<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amruth Kiran</style></author><author><style face="normal" font="default" size="100%">Praveen Kumar S E</style></author><author><style face="normal" font="default" size="100%">Tatiyana Mandal</style></author><author><style face="normal" font="default" size="100%">K Ganesh Shenoy</style></author><author><style face="normal" font="default" size="100%">Vasudev R Pai</style></author><author><style face="normal" font="default" size="100%">Swati Sharma</style></author><author><style face="normal" font="default" size="100%">Arul Amuthan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Acute Toxicity Study of the Crude Aqueous Extract of Tribulus terrestris Dried Fruit with Potential Diuretic Effect</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">acute toxicity study</style></keyword><keyword><style  face="normal" font="default" size="100%">crude aqueous extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Indian traditional medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Siddha system of medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Tribulus terrestris</style></keyword><keyword><style  face="normal" font="default" size="100%">Wistar Rats</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">566-576</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Tribulus terrestris&lt;/em&gt; is an important medicinal plant used in Indian traditional medicine, the crude aqueous extract of the plant is primarily used to induce diuresis for treating cardiovascular diseases and managing renal stones, etc... The safe dose and adverse effect profile of the extract was not explored adequately in preclinical studies. Hence, the present study was undertaken. &lt;strong&gt;Methods:&lt;/strong&gt; The acute toxicity was assessed based on the OECD guideline number 425: Acute Oral Toxicity – Up-and-Down-Procedure. A total of 11 animals were used in the study. Initially, one animal was administered with a dosage of 2000 mg/kg; and as the animal survived, four more animals were dosed and were observed for survival and other possible adverse drug reactions. The animals' body weight was measured before experimenting and at the end of the study. Biochemical and haematological examinations were done on normal control and test groups. Animals from the test group were sacrificed, and histopathological examinations of the vital organs were carried out. &lt;strong&gt;Results: &lt;/strong&gt;No signs of toxicity or changes in the behaviour were observed in the treatment group. As all the animals survived, it was decided that the LD&lt;sub&gt;50&lt;/sub&gt; was greater than 2000 mg/kg. However, the changes observed with platelets, total cholesterol and LDL were within the normal limits. Histological examination of the vital organs did not reveal any changes in the architecture of the organs. &lt;strong&gt;Conclusion:&lt;/strong&gt; Our study demonstrated that the crude aqueous extract of Tribulus terrestris dried fruit does not cause toxicity under the 2000 mg/kg dose limit.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">566</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Amruth Kiran&lt;sup&gt;1&lt;/sup&gt;, Praveen Kumar S E&lt;sup&gt;2&lt;/sup&gt;, Tatiyana Mandal&lt;sup&gt;1&lt;/sup&gt;, K Ganesh Shenoy&lt;sup&gt;1&lt;/sup&gt;, Vasudev R Pai&lt;sup&gt;3&lt;/sup&gt;, Swati Sharma&lt;sup&gt;4&lt;/sup&gt;, Arul Amuthan&lt;sup&gt;1,5,*&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Pharmacology, Department of Basic Medical Sciences, Manipal Academy of Higher Education, Manipal, India&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology, Manipal Tata Medical College, Manipal Academy of Higher Education, Manipal, INDIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacognosy, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, INDIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pathology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, INDIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Division of Siddha, Centre for Integrative Medicine and Research (CIMR), Manipal Academy of Higher Education, Manipal, India&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gornganok Piboonpol</style></author><author><style face="normal" font="default" size="100%">On-Anong Somsap</style></author><author><style face="normal" font="default" size="100%">Wanita Panthong</style></author><author><style face="normal" font="default" size="100%">Penporn Sujiwattanarat</style></author><author><style face="normal" font="default" size="100%">Anussara Kamnate</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antimicrobial and Antioxidant Activities of Phanera aureifolia (K.Larsen &amp; S.S.Larsen) Bandyop., P.P.Ghoshal &amp; M.K.Pathak Leaf Ethanolic Extracts</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimicrobial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoid compound</style></keyword><keyword><style  face="normal" font="default" size="100%">P.P.Ghoshal &amp; M.K.Pathak</style></keyword><keyword><style  face="normal" font="default" size="100%">Phanera aureifolia (K.Larsen &amp; S.S.Larsen) Bandyop.</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolic compound</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">365-369</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Natural antioxidants and antimicrobial agents are abundantly found in medicinal plants. &lt;strong&gt;Objective: &lt;/strong&gt;This study evaluated the antimicrobial and antioxidant activities of two colors from &lt;em&gt;Phanera aureifolia &lt;/em&gt;(K.Larsen &amp;amp; S.S.Larsen) Bandyop., P.P.Ghoshal &amp;amp; M.K.Pathak leaf ethanolic extracts including gold and green leaves. &lt;strong&gt;Method:&lt;/strong&gt; To assess antimicrobial efficacy, the agar well diffusion technique was analyzed. Scanning electron microscopy (SEM) was utilized to investigate the ultrastructural alterations in MRSA caused by leaf extracts. DPPH assay was used to assess antioxidant activity. The total amounts of phenolic compounds and flavonoids were evaluated through the Folin-Ciocalteu and aluminum chloride colorimetric techniques, respectively. The statistical analysis using an independent t-test. &lt;strong&gt;Results: &lt;/strong&gt;Both extracts demonstrated activity against &lt;em&gt;Pseudomonas aeruginosa &lt;/em&gt;TISTR146, &lt;em&gt;Micrococcus luteus&lt;/em&gt; TISTR884, &lt;em&gt;Staphylococcus aureus&lt;/em&gt; TISTR517 and Methicillin-resistant &lt;em&gt;S. aureus &lt;/em&gt;142 (MRSA142). Their activity against &lt;em&gt;M. luteus&lt;/em&gt; TISTR884 was the highest observed. The MIC of both extracts against MRSA were 10 mg/ml. SEM analysis revealed that the cells exhibited noticeable enlargement and swelling compared to untreated MRSA cells. Extract from the green leaves of Gold leaf Bauhinia showed greater radical scavenging activity, higher total phenolic and flavonoid contents, compared to those from the golden leaves. &lt;strong&gt;Conclusions: &lt;/strong&gt;The findings show that the extract from the green leaves of Gold leaf Bauhinia possess higher antioxidant potential compared to those from the golden leaves. In addition, both extracts exhibited antimicrobial activity, especially against MRSA.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">365</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Gornganok Piboonpol &lt;sup&gt;1*&lt;/sup&gt;, On-anong Somsap&lt;sup&gt;2&lt;/sup&gt;, Wanita Panthong&lt;sup&gt;2&lt;/sup&gt;, Penporn Sujiwattanarat&lt;sup&gt;2&lt;/sup&gt;, Anussara Kamnate&lt;sup&gt;3&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;1Department of Pharmacology, Faculty of medicine, Princess of Naradhiwas University, Narathiwat, Thailand&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;2Department of Biochemistry, Faculty of medicine, Princess of Naradhiwas University, Narathiwat, Thailand&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;3Department of Anatomy, Faculty of medicine, Princess of Naradhiwas University, Narathiwat, Thailand&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Anchana Babu</style></author><author><style face="normal" font="default" size="100%">Rekha D Kini</style></author><author><style face="normal" font="default" size="100%">Nayanatara Arun Kumar</style></author><author><style face="normal" font="default" size="100%">Megha Gokul</style></author><author><style face="normal" font="default" size="100%">Vandana Blossom</style></author><author><style face="normal" font="default" size="100%">Sreerag P</style></author><author><style face="normal" font="default" size="100%">Shymala Nayak</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antioxidant and Neuroprotective Potential of Ashwagandha In Aluminum-Induced Toxicity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Aluminum Chloride</style></keyword><keyword><style  face="normal" font="default" size="100%">Ashwagandha</style></keyword><keyword><style  face="normal" font="default" size="100%">Malondialdehyde</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidative stress</style></keyword><keyword><style  face="normal" font="default" size="100%">Reactive Oxygen Species</style></keyword><keyword><style  face="normal" font="default" size="100%">Reduced glutathione</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">336-341</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction : &lt;/strong&gt;Aluminium is the most abundant metal and the third most common element in the Earth’s crust, following oxygen and silicon. Exposure to aluminium is associated with oxidative damage, primarily due to its ability to disrupt redox balance, generate reactive oxygen species, and impair antioxidant defense mechanisms.This study was aimed to find the potential role of ashwagandha on aluminium induced brain toxicity. &lt;strong&gt;Methods: &lt;/strong&gt;In the present study rats were grouped into 4 groups of 6 rats in each. Brain tissue was removed and processed for biochemical and histopathological analysis. &lt;strong&gt;Results:&lt;/strong&gt; In the present study, administration of aluminium to rats resulted in a significant decrease in tissue GSH levels and a corresponding increase in MDA levels in the aluminium-treated group compared to the normal control.. Treatment with Ashwagandha showed a significant increase in GSH level and decrease in MDA level. Photomicrographic sections of the Brain in Ashwagandha-treated rats showed normla neuronal Count and exposure to Aluminium has caused significant reduction in the neuronal count. Experimental group pretreated with ashwagandha showed a visible increase in neuronal count in different regions of the rat brain.&lt;strong&gt; Conclusion: &lt;/strong&gt;The results revealed that oral administration of aluminium induced adverse oxidative effects in the exposed animals, while treatment with Ashwagandha markedly reduced the extent of aluminium chloride-induced brain injury.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">336</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Anchana Babu&lt;sup&gt;1&lt;/sup&gt;, Rekha D Kini&lt;sup&gt;1*&lt;/sup&gt;, Nayanatara Arun Kumar&lt;sup&gt;1&lt;/sup&gt;, Megha Gokul&lt;sup&gt;1&lt;/sup&gt;, Vandana Blossom&lt;sup&gt;2&lt;/sup&gt;, Sreerag P&lt;sup&gt;3&lt;/sup&gt;, Shymala Nayak&lt;sup&gt;4&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Physiology, Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Anatomy, Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Physiology, Srinivas Institute of Medical Sciences &amp;amp; Research Centre, Mukka, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biochemistry, Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">On-Anong Somsap</style></author><author><style face="normal" font="default" size="100%">Wasinee Poonsawat</style></author><author><style face="normal" font="default" size="100%">Ameena Benchamana</style></author><author><style face="normal" font="default" size="100%">Anussara Kamnate</style></author><author><style face="normal" font="default" size="100%">Gornganok Piboonpol</style></author><author><style face="normal" font="default" size="100%">Wanita Pantong</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anti-Tyrosinase, Anti-Inflammatory, and Cytotoxic Activity of Si Boo Gan Tang Rice and Rice Bran Extracts</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-tyrosinase</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">HaCaT cell</style></keyword><keyword><style  face="normal" font="default" size="100%">Si Boo Gan Tang Rice</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">22-27</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Si Boo Gan Tang is a widely cultivated variety of rice in the Tak Bai district of Narathiwat province, located in the southern region of Thailand. This study aimed to evaluate the biological properties of Si Boo Gan Tang rice and rice bran extracts, focusing on their anti-tyrosinase activity, anti-inflammatory activity, and cytotoxicity. The anti-tyrosinase assay revealed that the aqueous extract of rice (RW) significantly inhibited tyrosinase activity by 41.47%. Similarly, the ethanolic extract of rice (RE) exhibited anti-tyrosinase activity at 35.34%. The aqueous (RBW) and ethanolic (RBE) extracts of rice bran showed anti-tyrosinase activity with percentages of 19.26% and 29.08%, respectively. The anti-inflammatory experiment, conducted using RAW 264.7 cells, demonstrated that all extracts (RW, RBW, RE, and RBE) from rice and rice bran exhibited anti-inflammatory properties by reducing the release of nitric oxide (NO) from lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. The extracts had IC&lt;sub&gt;50&lt;/sub&gt; values of over 400 μg/ml and CC&lt;sub&gt;50&lt;/sub&gt; values over 400 μg/ml. Cytotoxicity was assessed using the MTT assay on HaCaT cells. The findings indicated that the IC&lt;sub&gt;50&lt;/sub&gt; values for both aqueous and ethanolic extracts of rice and rice bran were greater than 800 μg/ml.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">22</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;On-Anong Somsap&lt;sup&gt;1*&lt;/sup&gt;, Wasinee Poonsawat&lt;sup&gt;2&lt;/sup&gt;, Ameena Benchamana&lt;sup&gt;3&lt;/sup&gt;, Anussara Kamnate&lt;sup&gt;4&lt;/sup&gt;, Gornganok Piboonpol&lt;sup&gt;5&lt;/sup&gt;, Wanita Pantong&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biochemistry, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;The Center for Scientific and Technological Equipment, Walailak University, NaKhon Si Thammarat 80160, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Physiology, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Anatomy, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Pharmacology, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nefertiti EP</style></author><author><style face="normal" font="default" size="100%">Sudiarta KE</style></author><author><style face="normal" font="default" size="100%">Redemptus Y</style></author><author><style face="normal" font="default" size="100%">Biutifasari V</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Association Between Contraceptive Use and Pap Smear Findings in PKK Women in Bendul Merisi Surabaya</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cervical cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Contraceptives</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytology</style></keyword><keyword><style  face="normal" font="default" size="100%">Pap Smear</style></keyword><keyword><style  face="normal" font="default" size="100%">Uterine Cervix</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">642-643</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Cervical cancer remains a major health burden for women worldwide. Pap smear is a widely used screening tool, while contraceptive use, particularly hormonal methods, has been debated as a potential risk factor for cervical lesions. &lt;strong&gt;Objective:&lt;/strong&gt; This study aimed to investigate the association between contraceptive use and Pap smear findings among members of the Family Welfare Movement (PKK) in Bendul Merisi, Surabaya. &lt;strong&gt;Methods: &lt;/strong&gt;A cross-sectional study was conducted involving 64 respondents selected through purposive sampling. Data were collected using questionnaires and Pap smear results. Statistical analysis was performed using contingency coefficient tests. &lt;strong&gt;Results: &lt;/strong&gt;The study revealed a significant association between contraceptive use and Pap smear results (p = 0.001). Different types and duration of contraceptive use were significantly related to cytological outcomes, with hormonal methods showing a stronger association with abnormal findings such as LSIL (Low-grade Squamous Intraepithelial Lesion). &lt;strong&gt;Conclusions:&lt;/strong&gt; Contraceptive use, especially hormonal methods with longer duration, influences Pap smear findings, highlighting the need for regular cervical cancer screening among women using hormonal contraception&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">642</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nefertiti EP&lt;sup&gt;1&lt;/sup&gt;, Sudiarta KE&lt;sup&gt;2&lt;/sup&gt;, Redemptus Y&lt;sup&gt;3&lt;/sup&gt;, Biutifasari V&lt;sup&gt;4&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anatomical Pathology, Faculty of Medicine, Hang Tuah University, Surabaya, East Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Obstetrics Gynecology, Faculty of Medicine, Hang Tuah University, Surabaya, East Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Surgery, Faculty of Medicine, Hang Tuah University, Surabaya, East Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Clinical Pathology, Faculty of Medicine, Hang Tuah University, Surabaya, East Java, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pallab Kar</style></author><author><style face="normal" font="default" size="100%">Ayodeji O. Oriola</style></author><author><style face="normal" font="default" size="100%">Adebola O. Oyedeji</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Characterization of Green Synthesized Silver Nanoparticles from Clerodendrum thomsoniae Balf.f., and Their Antioxidant and Anti inflammatory Potential</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Clerodendrum thomsoniae; silver nanoparticles; antioxidant; anti-inflammatory</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">676-682</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Medicinal plant extracts and other natural products have continued to find useful applications in nanomedicines due to their interesting biological properties. &lt;em&gt;Clerodendrum thomsoniae&lt;/em&gt; (CT) is a plant used in traditional medicine to treat stress- and inflammation-related diseases, including jaundice, diabetes, and cancer. Objectives: This study, therefore, evaluated CT extract-based silver nanoparticles (Ag NPs) for their antioxidant and anti-inflammatory potential. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The nanoparticles were prepared using green synthesis methods. They were characterized using UVVis spectroscopy, scanning electron microscopy (SEM), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), and X-ray diffraction (XRD). Antioxidant study was based on NO, H2O2, superoxide, and hydroxyl radical scavenging spectrophotometric methods. The&lt;em&gt; in vitro &lt;/em&gt;anti-inflammatory test was based on a protein (egg albumin) denaturation assay. &lt;strong&gt;Results: &lt;/strong&gt;Results showed CT-Ag NPs ranged from spherical to cubic shapes. The UV absorption peak at 427 nm suggests CT-Ag NP formation. The presence of elemental Ag (96.04 %) by EDX analysis suggests the conversion of metallic silver into elemental silver. The crystallinity of the nanoparticles was shown on the X-ray diffractogram as a sharp peak at 38.12° [reflection index (111)] with an average particle size of 47 nm. CT-Ag NPs showed dose-dependent hydroxyl and nitric oxide radical scavenging activities with 67.63 ± 0.78 % and 58.48 ± 1.20 %, respectively, at 200 μg/mL. It showed a notable anti-inflammatory effect by inhibiting protein denaturation with an IC50 of 53.58 ± 17.78 μg/mL.&lt;strong&gt; Conclusions: &lt;/strong&gt;It can be deduced from this study that CT-Ag NPs show promise as antioxidant and anti-inflammatory agents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">676</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Pallab Kar&lt;sup&gt;1*&lt;/sup&gt;, Ayodeji O. Oriola&lt;sup&gt;2*&lt;/sup&gt;, Adebola O. Oyedeji&lt;sup&gt;1,2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;African Medicinal Flora and Fauna Research Niche, Walter Sisulu University, Nelson Mandela Drive, P/Bag X1, Mthatha 5117, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemical and Physical Sciences, Walter Sisulu University, Nelson Mandela Drive, P/ Bag X1, Mthatha 5117, SOUTH AFRICA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Neethi T P</style></author><author><style face="normal" font="default" size="100%">Prashanth Kumar C</style></author><author><style face="normal" font="default" size="100%">Chaitra Uppangala</style></author><author><style face="normal" font="default" size="100%">Barbara Coelho</style></author><author><style face="normal" font="default" size="100%">Nayanatara Arun Kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Evaluation of Dexmedetomidine versus Fentanyl Added to Hyperbaric Levobupivacaine for Subarachnoid Block: Effects on Sensory-Motor Blockade and Analgesic Duration</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">abdominal hysterectomy</style></keyword><keyword><style  face="normal" font="default" size="100%">Dexmedetomidine</style></keyword><keyword><style  face="normal" font="default" size="100%">Fentanyl</style></keyword><keyword><style  face="normal" font="default" size="100%">levobupivacaine</style></keyword><keyword><style  face="normal" font="default" size="100%">spinal anesthesia</style></keyword><keyword><style  face="normal" font="default" size="100%">subarachnoid block</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">638-641</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction :&lt;/strong&gt; Adjuvants to local anesthetics enhance the quality and duration of spinal anesthesia while reducing postoperative analgesic requirements. Opioids like fentanyl are effective but associated with significant side effects, whereas dexmedetomidine, an α2-adrenergic agonist, has shown promise as a non-opioid alternative. &lt;strong&gt;Objective : &lt;/strong&gt;To compare the effects of intrathecal dexmedetomidine and fentanyl, when added to levobupivacaine, on sensory and motor block characteristics, duration of analgesia, and complications in patients undergoing elective total abdominal hysterectomy. &lt;strong&gt;Methods: &lt;/strong&gt;In this prospective, double-blind, randomized controlled trial, 60 ASA I–II female patients aged 18–65 years were allocated into two groups (n = 30 each). Group D received 15 mg 0.5% hyperbaric levobupivacaine with 5 μg dexmedetomidine, and Group F received 15 mg 0.5% hyperbaric levobupivacaine with 25 μg fentanyl intrathecally. Block onset, duration of sensory and motor blockade, time to first rescue analgesia, hemodynamic changes, and side effects were recorded. &lt;strong&gt;Results: &lt;/strong&gt;Demographic variables were comparable between groups. The onset of sensory and motor block was significantly faster with fentanyl, while dexmedetomidine prolonged the duration of sensory block (458.83 vs 358.07 min, &lt;em&gt;p &lt;/em&gt;&amp;lt; 0.001), motor block (287.33 vs 217.33 min&lt;em&gt;, p&lt;/em&gt; &amp;lt; 0.001), and time to rescue analgesia (95.5 vs 55.5 min,&lt;em&gt; p &lt;/em&gt;&amp;lt; 0.001). Hypotension was the most common complication in both groups, without significant difference between two groups. Pruritus was observed only in the fentanyl group, while bradycardia was rare and not significant in the dexmedetomidine group. &lt;strong&gt;Conclusion: I&lt;/strong&gt;ntrathecal dexmedetomidine, as an adjuvant to levobupivacaine, provides prolonged sensory and motor block and superior postoperative analgesia compared to fentanyl, with fewer side effects. It may be considered a preferable adjuvant for spinal anesthesia in total abdominal hysterectomy&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">638</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Neethi T P&lt;sup&gt;1&lt;/sup&gt;, Prashanth Kumar C&lt;sup&gt;2&lt;/sup&gt;, Chaitra Uppangala&lt;sup&gt;3*&lt;/sup&gt;, Barbara Coelho&lt;sup&gt;2&lt;/sup&gt;, Nayanatara Arun Kumar&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anesthesiology, P K DAS Institute of Medical Sciences Palakkad, Kerala,INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Anesthesiology, Srinivas Institute of Medical Sciences and Research Centre, Mangalore, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Physiology, Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, India.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Patcharin Singdam</style></author><author><style face="normal" font="default" size="100%">Anussara Kamnate</style></author><author><style face="normal" font="default" size="100%">On-Anong Somsap</style></author><author><style face="normal" font="default" size="100%">Ruhainee Tohkayomatee</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Phytochemical, Antioxidant, and Antibacterial Study of Different Solvent Extracts of Cissus hastata Leaves</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Cissus hastata</style></keyword><keyword><style  face="normal" font="default" size="100%">Leaves</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">511-519</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Plants have long been utilized in traditional medicine for treating a variety of diseases. Plant-derived extracts are a rich source of phytochemicals with documented antibacterial and antioxidant properties. &lt;strong&gt;Objective:&lt;/strong&gt; This study aimed to investigate and compare the phytochemical profiles, antioxidant capacities, and antibacterial activities of various crude extracts from the leaves of &lt;em&gt;Cissus hastata.&lt;/em&gt; &lt;strong&gt;Methods: &lt;/strong&gt;Leaf extracts of &lt;em&gt;C. hastata&lt;/em&gt; were prepared using hexane (Hex), ethyl acetate (EtOAc), 95% ethanol (EtOH), and 50% ethanol (AqE). These extracts were analyzed for preliminary phytochemical constituents, total phenolic content (TPC), total flavonoid content (TFC), antioxidant activity (DPPH, ABTS, and FRAP assays), and antibacterial activity against five bacterial strains: Staphylococcus aureus (TISTR 517), methicillin-resistant &lt;em&gt;Staphylococcus aureus&lt;/em&gt; (MRSA 142)&lt;em&gt;, Bacillus cereus&lt;/em&gt; (ATCC 11778), &lt;em&gt;Escherichia coli &lt;/em&gt;(ESBL 182), and &lt;em&gt;Salmonella typhimurium &lt;/em&gt;(TISTR 292). &lt;strong&gt;Results: &lt;/strong&gt;Phytochemical screening of different solvent extracts of &lt;em&gt;C. hastata&lt;/em&gt; leaves revealed the presence of diverse bioactive compounds. The EtOAc and AqE extracts exhibited the highest TPC (65.31 ± 1.85 and 61.45 ± 3.34 mg GAE/g extract, respectively) (&lt;em&gt;p&lt;/em&gt; &amp;lt; 0.05). In contrast, the EtOH extract showed the highest TFC (29.92 ± 3.42 mg QE/g extract) (p &amp;lt; 0.05). The EtOH and AqE extracts also demonstrated the strongest antioxidant activities in the DPPH (IC50: 307.07 ± 7.18 μg/mL and 316.86 ± 11.78 μg/mL), ABTS (IC50: 160.21 ± 5.43 μg/mL and 208.45 ± 3.84 μg/ mL) (p &amp;lt; 0.05), and FRAP (4.69 ± 0.08 and 4.96 ± 0.07 mM FeSO4/mg extract) assays. The antibacterial activity was observed exclusively against Gram-positive bacteria. Among all the extracts, the AqE extract at a concentration of 100 mg/mL exhibited significant antibacterial effects against Staphylococcus aureus, methicillin-resistant Staphylococcus aureus, and Bacillus cereus, with zones of inhibition measuring 15.43 ± 0.46 mm, 14.76 ± 0.58 mm, and 15.66 ± 1.04 mm, respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; Ethanol-based extracts of&lt;em&gt; C. hastata&lt;/em&gt; leaves demonstrate high antioxidant and antibacterial activities and represent a promising source of bioactive compounds for developing natural therapeutic agents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">511</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Patcharin Singdam&lt;sup&gt;1*&lt;/sup&gt;, Anussara Kamnate&lt;sup&gt;2&lt;/sup&gt;, On-Anong Somsap&lt;sup&gt;3&lt;/sup&gt;, Ruhainee Tohkayomatee&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Anatomy, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biochemistry, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Thidarut Kwuansawat</style></author><author><style face="normal" font="default" size="100%">Suwakrit Sriplee</style></author><author><style face="normal" font="default" size="100%">Phattharawadee Meelek</style></author><author><style face="normal" font="default" size="100%">Patcharawan Sujayanont</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comprehensive Antioxidant Evaluation of Tiliacora triandra Extracts: Assays of Leaf, Stem, and Root</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">Five roots</style></keyword><keyword><style  face="normal" font="default" size="100%">Tiliacora triandra</style></keyword><keyword><style  face="normal" font="default" size="100%">Yanang</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">95-98</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This study evaluates the antioxidant potential of &lt;em&gt;Tiliacora triandra &lt;/em&gt;(locally known as “Yanang”) extracts from the leaves, stems, and roots using three established assays: DPPH (2,2-diphenyl-1-picrylhydrazyl), ABTS (2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid)), and FRAP (ferric reducing antioxidant power). The extracts were prepared using 95% ethanol, and their antioxidant activities were assessed in terms of IC50 and Trolox equivalents. The DPPH assay yielded IC&lt;sub&gt;50&lt;/sub&gt; values of 187.91±28.09 μg/ml, 85.93±10.91 μg/ml, and 71.31±11.29 μg/ml for the leaf, stem, and root extracts, respectively. Similarly, the ABTS assay showed IC50 values of 181.78±22.96 μg/ml for the leaf extract, 70.07±6.40 μg/ml for the stem extract, and 48.09±8.77 μg/ml for the root extract. In both assays, the root and stem extracts exhibited comparable antioxidant activity, whereas the leaf extract showed significantly lower activity (p &amp;lt; 0.05). The FRAP assay revealed no significant differences among the extracts, with Trolox equivalent values ranging from 190 to 211 mg TE/g extract. These findings suggest that the root and stem extracts possess strong antioxidant activity and may be used interchangeably in applications requiring such properties, whereas the leaf extract has comparatively lower potential. Further studies are recommended to explore the therapeutic properties and potential health benefits of these extracts.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">95</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Thidarut Kwuansawat&lt;sup&gt;1&lt;/sup&gt;, Suwakrit Sriplee&lt;sup&gt;2&lt;/sup&gt;, Phattharawadee Meelek&lt;sup&gt;2&lt;/sup&gt;, Patcharawan Sujayanont&lt;sup&gt;3,4*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Applied Thai Traditional Medicine, Faculty of Medicine, Mahasarakham University, Maha Sarakham 44000, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Bachelor of Applied Thai Traditional Medicine, Faculty of Medicine, Mahasarakham University, Maha Sarakham 44000, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Preclinical Department, Faculty of Medicine, Mahasarakham University, Maha Sarakham 44000, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Tropical Health Innovation Research Unit, Mahasarakham University, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aasia Kanwal</style></author><author><style face="normal" font="default" size="100%">Muhammad Hamdi Mahmood</style></author><author><style face="normal" font="default" size="100%">Mahad Butt</style></author><author><style face="normal" font="default" size="100%">Hidayat Ur Rahman</style></author><author><style face="normal" font="default" size="100%">Norhida Ramli</style></author><author><style face="normal" font="default" size="100%">Saiful Bahri Talip</style></author><author><style face="normal" font="default" size="100%">Showkat Ahmad Bhawani</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Components of Gamma Oryzanol on Toll-Like Receptor 4: Receptor Structure-Based Pharmacophore, Hit Identification, and In Silico Evidence</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory</style></keyword><keyword><style  face="normal" font="default" size="100%">Gamma oryzanol</style></keyword><keyword><style  face="normal" font="default" size="100%">Infertility</style></keyword><keyword><style  face="normal" font="default" size="100%">Polycystic ovarian syndrome</style></keyword><keyword><style  face="normal" font="default" size="100%">TLR4 antagonist</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">329-335</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Polycystic ovarian syndrome is a leading cause of female infertility. Inflammation has a central role in infertility. Persistent activation of Toll-like receptor 4 contributes to inflammation in PCOS. Gamma-oryzanol consists of esters of ferulic acid combined with phytosterols and triterpene alcohol derivatives of rice bran oil, and is known to have anti-inflammatory effects. However, the structural interaction of different gamma-oryzanol compounds with TLR4 remains unknown. &lt;strong&gt;Objectives: &lt;/strong&gt;The study aimed to investigate gamma oryzanol compounds as hit compounds and inhibitors of Toll-like receptor 4 by developing a pharmacophore model through a receptor structure-based approach coupled with molecular docking studies with the Molecular Operating Environment (MOE) software. &lt;strong&gt;Methods: &lt;/strong&gt;A structure-based pharmacophore model was generated from the co-crystalized structure of the TLR4– MD2 complex. Gamma-oryzanol derivatives were evaluated against the constructed pharmacophore model to identify potential hit compounds. The potential hit compounds that satisfied essential pharmacophoric features were subjected to molecular docking with TLR4. &lt;strong&gt;Results:&lt;/strong&gt; The pharmacophore consisted of three characteristics: a hydrogen bond donor, a hydrogen bond acceptor, and a hydrophobic. Cycloartenyl ferulate, 24-methylenecycloartenyl ferulate, Campesteryl ferulate, and β-sitosteryl ferulate were found to be the hit compounds against the generated pharmacophore. The docking experiment showed that Cycloartenyl ferulate had the most potent binding interaction with TLR4 (7.9933), followed by 24-methylenecycloartenyl ferulate (-7.8580), Campesteryl ferulate (-6.1675), and β-sitosteryl ferulate (-5.9673). &lt;strong&gt;Conclusion: &lt;/strong&gt;The present pharmacophore modeling and docking findings predict that gammaoryzanol may bind with the TLR4 ligand binding domain, providing structural insights into their therapeutic potential role as a modulator of the TLR4-mediated inflammatory pathway. These findings provide a theoretical foundation for future in vitro and in vivo validation studies aimed at elucidating the mechanistic basis of gamma-oryzanol’s anti-inflammatory activity in PCOS.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">329</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Aasia Kanwal&lt;sup&gt;1*&lt;/sup&gt;, Muhammad Hamdi Mahmood&lt;sup&gt;1&lt;/sup&gt;, Mahad Butt&lt;sup&gt;2&lt;/sup&gt;, Hidayat Ur Rahman&lt;sup&gt;1&lt;/sup&gt;, Norhida Ramli&lt;sup&gt;1&lt;/sup&gt;, Saiful Bahri Talip&lt;sup&gt;1&lt;/sup&gt;, Showkat Ahmad Bhawani&lt;sup&gt;3&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Medicine &amp;amp; Health Sciences, Universiti Malaysia Sarawak, 94300 Kota Samarahan, MALAYSIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medicine, Allama Iqbal Medical College, 54550 Lahore, PAKISTAN. 3Faculty of Resource Science and Technology, Universiti Malaysia Sarawak, 94300 Kota Samarahan, MALAYSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Urarat Nanna</style></author><author><style face="normal" font="default" size="100%">Jarinyaporn Naowaboot</style></author><author><style face="normal" font="default" size="100%">Linda Chularojmontri</style></author><author><style face="normal" font="default" size="100%">Rawiwun Kaewamatawong</style></author><author><style face="normal" font="default" size="100%">Sudarat Homhual</style></author><author><style face="normal" font="default" size="100%">Suvara Wattanapitayakul</style></author><author><style face="normal" font="default" size="100%">Wanwisa Suwannaloet</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of Citrus aurantifolia Root Ethanolic Extract on Lipogenesis in Palmitate-Induced Lipid Accumulation in HepG2 Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Citrus aurantifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">Lipid metabolism</style></keyword><keyword><style  face="normal" font="default" size="100%">Lipogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Nonalcoholic fatty liver disease</style></keyword><keyword><style  face="normal" font="default" size="100%">Obesity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">77-83</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Citrus aurantifolia &lt;/em&gt;(lime) is mostly found in tropical and subtropical region. The lime peel and lime juice extracts have antioxidant, antidiabetic and anti-inflammatory effects. However, the pharmacological effects of the lime root remain widely unknown. Thus, the current study investigated the effects of &lt;em&gt;Citrus aurantifolia&lt;/em&gt; root ethanolic extract (CA) on lipogenesis induced by palmitic acid (PA) in HepG2 cells. &lt;strong&gt;Methods: &lt;/strong&gt;The PA-induced lipogenesis in HepG2 cells was used for measuring lipogenic gene expression and lipid accumulation of CA. Phytochemical content was also determined in CA. &lt;strong&gt;Results: &lt;/strong&gt;In PA-treated group showed the state of hepatic lipid accumulation with increased lipogenic gene, acetyl-CoA carboxylase (ACC), fatty acid synthase (FAS) and sterol regulatory element binding protein1c (SREBP1c) as compared to the control group. Interestingly, administration of CA (5-10 μg/mL) effectively reduced lipid storage and significantly decreased the expression of these lipogenic gene in PA-treated cells. Notably, CA treatment increased the gene expression of fatty acid oxidation, carnitine palmitoyl transferase 1A (CPT1A) and peroxisome proliferator-activated receptor α (PPARα). Furthermore, this study found that the major bioactive component from CA was nordentatin (coumarin group).&lt;strong&gt; Conclusions:&lt;/strong&gt; The results indicated that the CA treatment might be a useful agent for improving abnormal lipid metabolism in obesity-related nonalcoholic fatty liver disease.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">77</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Urarat Nanna&lt;sup&gt;1&lt;/sup&gt;, Jarinyaporn Naowaboot&lt;sup&gt;1&lt;/sup&gt;, Linda Chularojmontri&lt;sup&gt;1&lt;/sup&gt;, Rawiwun Kaewamatawong&lt;sup&gt;2&lt;/sup&gt;, Sudarat Homhual&lt;sup&gt;2&lt;/sup&gt;, Suvara Wattanapitayakul&lt;sup&gt;3&lt;/sup&gt;, Wanwisa Suwannaloet&lt;sup&gt;4*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Preclinical Science, Faculty of Medicine, Thammasat University, Pathum Thani 12120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Pharmaceutical Sciences, Ubon Ratchathani University, Ubon Ratchathani, 34190, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacology, Faculty of Medicine, Srinakharinwirot University, Bangkok 10110, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;College of Medicine and Public Health, Ubon Ratchathani University, Ubon Ratchathani, 34190, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ashwani Kumar</style></author><author><style face="normal" font="default" size="100%">Prikshat Kumar Angra</style></author><author><style face="normal" font="default" size="100%">Suresh Chandra Akula</style></author><author><style face="normal" font="default" size="100%">Pritpal Singh</style></author><author><style face="normal" font="default" size="100%">Anuj Sharma</style></author><author><style face="normal" font="default" size="100%">Anup Sharma</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efficacy of Standardized Withania Somnifera as Neuro Agent in Tension-Type Headache: A Comparative Trial of Data in Transit</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biomarker Integrity</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical Standardization</style></keyword><keyword><style  face="normal" font="default" size="100%">Sustainable Research Framework</style></keyword><keyword><style  face="normal" font="default" size="100%">Tension-Type Headache</style></keyword><keyword><style  face="normal" font="default" size="100%">Withania somnifera</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">378-385</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; To evaluate the role of withania somnifera as a neuro-psychiatric agent in the treatment of Tension-Type Headache (TTH), there is a need to substantiate the therapy using solid therapeutic evidence. Although using traditional medicine has a great potential, it is difficult to demonstrate the efficacy of a particular phytochemical composition regarding the frequency of and physiological stress markers of the chronic Tension-Type Headache in standardized research. &lt;strong&gt;Objective: &lt;/strong&gt;The purpose of the study is to assess the therapeutic efficacy of a standardized Withania somnifera extract in reducing the frequency of and physiological stress markers of the chronic Tension-Type Headache. Methods: We used the study as a double-blind and randomized controlled trial (RCT). The subjects were randomly selected to be given a standardized extract of the root of W. somnifera, that has been titrated to contain 5 percent withanolides, or a placebo dose of 60 days. The paper ensured a rigorous &quot;molecular chain of custody&quot; with a batch of withanolides linked in clinical outcome reported where the mean frequency of headaches in the treatment group reduced by 42% (p [Less than] 0.005). &lt;strong&gt;Results:&lt;/strong&gt; Clinical outcome showed that there was a significant decline in the frequency of headaches in the treatment group by 42% (p [Less than] 0.005). Moreover, the Ashwagandha group was showing a significant drop in salivary cortisol levels, which means that there was a decrease in the level of physiological stress response to chronic TTH. &lt;strong&gt;Conclusion:&lt;/strong&gt; Standardized natural products should be integrated into clinical trials as it is the most beneficial to the development of sustainable pharmacognosy. This experiment can offer an unambiguous evidence base, a clear and reproducible basis of evidence regarding the use of Ashwagandha in the current neurological practice by showing the clear efficacy in reducing the frequency of Tension-Type Headaches and biological stress markers.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">378</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ashwani Kumar&lt;sup&gt;2*&lt;/sup&gt;, Prikshat Kumar Angra&lt;sup&gt;2&lt;/sup&gt;, Suresh Chandra Akula&lt;sup&gt;1&lt;/sup&gt;, Pritpal Singh&lt;sup&gt;1&lt;/sup&gt;, Anuj Sharma&lt;sup&gt;2&lt;/sup&gt;, Anup Sharma&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Mittal School of Business, Lovely Professional University, Phagwara, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;School of Computer Applications, Lovely Professional University, Phagwara, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Abhinav Dutta</style></author><author><style face="normal" font="default" size="100%">Jyothi Sujan Prasad</style></author><author><style face="normal" font="default" size="100%">Pradyum Anand</style></author><author><style face="normal" font="default" size="100%">Chandrashekar K.S</style></author><author><style face="normal" font="default" size="100%">Venkatesh Kamath B</style></author><author><style face="normal" font="default" size="100%">Vijaya Bhaskar K</style></author><author><style face="normal" font="default" size="100%">Aswatha Ram H.N</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Formulation and Analytical Evaluation of Herbal Rectal Suppositories Containing Senna Extract for the Management of Constipation</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Glycerine</style></keyword><keyword><style  face="normal" font="default" size="100%">herbal suppositories</style></keyword><keyword><style  face="normal" font="default" size="100%">senna extract</style></keyword><keyword><style  face="normal" font="default" size="100%">suppositories</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">438-443</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background.&lt;/strong&gt; Senna is a commonly used stimulant laxative that is typically administered orally as a senna extract tablet to treat constipation. This study aimed to formulate rectal suppositories containing senna extract, using glycerin as a base, to achieve site-specific drug delivery and reduce systemic side effects. &lt;strong&gt;Methodology. &lt;/strong&gt;The prepared suppositories were evaluated for various physicochemical and performance parameters, including visual appearance, disintegration time, in vitro dissolution, melting point, weight uniformity, drug content and HPTLC. &lt;strong&gt;Results.&lt;/strong&gt; The suppositories demonstrated satisfactory physical characteristics, with an average weight of 0.9707 g and a drug content of 0.150 ± 2% mg per suppository. The melting point was recorded at 37°C, and the complete dispersion time was 30 minutes. In vitro drug release studies revealed that the drug was fully released within 45 minutes. High-performance thin layer chromatography (HPTLC) was utilized to confirm the presence of active constituents by comparing the sample profile with that of a standard extract. &lt;strong&gt;Conclusion. &lt;/strong&gt;These findings suggest that senna extract suppositories are a promising alternative to oral tablets, providing targeted drug delivery through the rectal route for improved therapeutic outcomes.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">438</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Abhinav Dutta&lt;sup&gt;1&lt;/sup&gt;, Jyothi Sujan Prasad&lt;sup&gt;1&lt;/sup&gt;, Pradyum Anand&lt;sup&gt;1&lt;/sup&gt;, Chandrashekar K.S.&lt;sup&gt;1&lt;/sup&gt;, Venkatesh Kamath B&lt;sup&gt;2&lt;/sup&gt;, Vijaya Bhaskar K&lt;sup&gt;3&lt;/sup&gt;, Aswatha Ram H.N.&lt;sup&gt;1*&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal-576104, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Biotechnology, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal-576104, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmaceutical Chemistry, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal-576104, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Babiker Bashir Haroun Baraka</style></author><author><style face="normal" font="default" size="100%">Bhagya Venkanna Rao</style></author><author><style face="normal" font="default" size="100%">Tanuja Krishnamurthy</style></author><author><style face="normal" font="default" size="100%">Ramya Vasudev</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Housing In An Enriched Environment Enhances The Neuroprotective Effect Of Celastrus Paniculatus And Tribulus Terrestris In An Animal Model Of Chronic Stress</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chronic Immobilization stress</style></keyword><keyword><style  face="normal" font="default" size="100%">Depression</style></keyword><keyword><style  face="normal" font="default" size="100%">Enriched Environment</style></keyword><keyword><style  face="normal" font="default" size="100%">Hippocampus</style></keyword><keyword><style  face="normal" font="default" size="100%">Neurotrophic factor</style></keyword><keyword><style  face="normal" font="default" size="100%">Pro-inflammatory cytokines</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">191-202</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Prolonged exposure to stress can contribute to depressive episodes. Preclinical studies have shown that stimuli like environmental enrichment (EE) can produce beneficial effects against stress by positively modulating neuroplasticity, neurochemistry, and behaviour. Hence, we explored whether exposure to EE can augment the neuroprotective activities of &lt;em&gt;Celastrus paniculatus&lt;/em&gt; (CP) and &lt;em&gt;Tribulus terrestris&lt;/em&gt; (TT) in stressed conditions. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Rats were placed in immobilisation bags and stressed for two hours a day for ten days. After that, these stressed rats were treated by CP or TT, alone or in combination with enriched housing. Behavioural analysis in elevated plus maze, open field, forced swim and sucrose preference tests. The novel object recognition test and the rewarded alteration test on the T-maze were used to assess working memory. The brain-derived neurotrophic factor, interleukin-6, and tumour necrotic factor-alpha were measured in the hippocampus and prefrontal cortical tissues following stress and herbal treatment combined with an enriched environment.&lt;strong&gt; Results: &lt;/strong&gt;We found that &lt;em&gt;Celastrus paniculatus&lt;/em&gt; and &lt;em&gt;Tribulus terrestris&lt;/em&gt;, combined with an enriched environment, produced a synergistic neuroprotective effect. CP + EE and TT + EE improved working memory and recognition memory in CIS animals, but they also reduced anxiety and depressive-like behaviours. TNF-α and IL-6 levels were decreased while brain-derived neurotrophic factor levels were raised in the frontal cortex and hippocampus regions, respectively.&lt;strong&gt; Conclusion: &lt;/strong&gt;Our results show that living in an enriched environment can improve CP and TT neuromodulatory activities, highlighting the potential of combining sensory-motor interventions with herbal remedies for psychiatric disorders.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">191</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Babiker Bashir Haroun Baraka&lt;sup&gt;1,2&lt;/sup&gt;, Bhagya Venkanna Rao&lt;sup&gt;1*&lt;/sup&gt;, Tanuja Krishnamurthy&lt;sup&gt;1&lt;/sup&gt;, Ramya Vasudev&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, KLE College of Pharmacy, KLE Academy of Higher Education and Research Rajajinagar, Bengaluru-560010, Karnataka, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Dr.Prabhakar B Kore Basic Science Research Centre, KLE College of Pharmacy, KLE Academy of Higher Education and Research Rajajinagar, Bengaluru-560010, Karnataka, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Uratchat Vichaidit</style></author><author><style face="normal" font="default" size="100%">Chuntida Kamalashiran</style></author><author><style face="normal" font="default" size="100%">Kammal Kumar Pawa</style></author><author><style face="normal" font="default" size="100%">Pratya Phetkate</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hydrolyzed Collagen Tonic Drink Prevents Worsening of Skin Parameters and Improves Photoaging Classification in Healthy Thai Women: A Randomized Controlled Trial</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Dermal aging</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrolyzed collagen</style></keyword><keyword><style  face="normal" font="default" size="100%">photoaging</style></keyword><keyword><style  face="normal" font="default" size="100%">Skin elasticity</style></keyword><keyword><style  face="normal" font="default" size="100%">Wrinkle</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">644-652</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Skin aging represents a significant public health burden globally, with Southeast Asian populations experiencing accelerated photoaging due to intensive environmental ultraviolet exposure. &lt;strong&gt;Aim: &lt;/strong&gt;To evaluate the preventive efficacy of hydrolyzed collagen tonic drink on skin aging parameters in healthy Thai women. &lt;strong&gt;Methods: &lt;/strong&gt;A double-blind, randomized controlled trial was conducted with 135 Thai women aged 40-60 years. Participants were randomized to receive either hydrolyzed fish collagen peptides with supportive nutrients (n=67) or active fruit juice control (n=68) daily for 12 weeks. Primary outcomes included skin microtopography parameters measured by Visioscan, skin elasticity assessed by Cutometer, and clinical photoaging classification using Glogau scale. Secondary outcomes examined molecular biomarker changes in procollagen Type I synthesis. &lt;strong&gt;Results:&lt;/strong&gt; The collagen group demonstrated significantly attenuated skin surface deterioration compared to placebo. The Wrinkles parameter showed significant betweengroup differences at week 8 (-100.43 units, p=0.001). Smoothness parameter exhibited protective effects with significant between-group differences at week 8 (-80.08 units, p=0.002). Gross elasticity improved significantly within the collagen group at week 12 (p=0.033). Procollagen Type I synthesis demonstrated superior maintenance in the collagen group versus placebo (between-group percent change difference, p=0.002). Both groups achieved comparable Glogau classification improvements (23.9% versus 20.6%). &lt;strong&gt;Conclusion: &lt;/strong&gt;Daily hydrolyzed collagen supplementation with supportive nutrients effectively prevented skin surface parameter deterioration in Thai women, demonstrating meaningful preservation of skin integrity through medium effect sizes for key parameters. These findings support nutritional approaches as complementary strategies for photoaging management in high ultraviolet-exposure populations&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">644</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Uratchat Vichaidit&lt;sup&gt;1&lt;/sup&gt;, Chuntida Kamalashiran&lt;sup&gt;1&lt;/sup&gt;, Kammal Kumar Pawa&lt;sup&gt;1&lt;/sup&gt;, Pratya Phetkate&lt;sup&gt;1*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Integrative Medicine, Chulabhorn International College of Medicine, Thammasat University (Rangsit Campus), Pathum Thani, 12120, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vishu Manchanda</style></author><author><style face="normal" font="default" size="100%">Bhagyalakshmi K</style></author><author><style face="normal" font="default" size="100%">Nayanatara Arun Kumar</style></author><author><style face="normal" font="default" size="100%">Anupama N</style></author><author><style face="normal" font="default" size="100%">Rekha D Kini</style></author><author><style face="normal" font="default" size="100%">Sneha Shetty</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Intermittent Fasting as a Non-Invasive Strategy to Mitigate Diabetes-Induced Complications in Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Intermittent fasting; Type 2 diabetes mellitus; Alloxan; Wistar rats; Physiological changes; Biochemical parameters; Histological changes</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">632-637</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The global burden of diabetes mellitus is steadily increasing. Abnormal eating patterns and excess energy intake contribute to obesity and type 2 diabetes mellitus (T2DM). Although dietary modifications such as intermittent fasting have gained attention, evidence supporting their beneficial role in T2DM is limited. &lt;strong&gt;Objective: &lt;/strong&gt;To evaluate the beneficial effects of intermittent fasting on physiological, biochemical, and histological changes in a rat model of type 2 diabetes mellitus. &lt;strong&gt;Methods:&lt;/strong&gt; Healthy adult Wistar albino rats (150–200 g) were used. Diabetes was induced by administering alloxan (150 mg/kg). Animals were divided into four groups: Normal Control (Group I), Experimental Control (Group II), and Intermittent Fasting groups (Group III &amp;amp; Group IV). Physiological, biochemical, and histological parameters were assessed to determine the impact of intermittent fasting. Results: Intermittent fasting demonstrated a protective effect by reducing diabetes-induced physiological, biochemical, and histological alterations. Rats in the intermittent fasting groups showed improved outcomes compared to the experimental control group. &lt;strong&gt;Conclusion:&lt;/strong&gt; Intermittent fasting may serve as a potential non-invasive strategy to reduce diabetesrelated complications. Further studies focusing on molecular mechanisms are warranted to provide deeper insights into its protective role.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">632</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Vishu Manchanda&lt;sup&gt;1&lt;/sup&gt;, Bhagyalakshmi K&lt;sup&gt;1*&lt;/sup&gt;, Nayanatara Arun Kumar&lt;sup&gt;1&lt;/sup&gt;, Anupama N&lt;sup&gt;1&lt;/sup&gt;, Rekha D Kini&lt;sup&gt;1&lt;/sup&gt;, Sneha Shetty&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Physiology, Kasturba Medical College Mangalore, Manipal Academy Higher Education, Manipal, India&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Enkhtuul Bayarsaikhan</style></author><author><style face="normal" font="default" size="100%">Turtushikh Damba</style></author><author><style face="normal" font="default" size="100%">Buyanjargal Erdenebat</style></author><author><style face="normal" font="default" size="100%">Norovnyam Ryenchinbyambaa</style></author><author><style face="normal" font="default" size="100%">Otgonsuren Daramzav</style></author><author><style face="normal" font="default" size="100%">Khuvitavilan Battulga</style></author><author><style face="normal" font="default" size="100%">Munkhzul Boldbaatar</style></author><author><style face="normal" font="default" size="100%">Myagmarsuren Badamtsetseg</style></author><author><style face="normal" font="default" size="100%">Enkhjargal Dorjval</style></author><author><style face="normal" font="default" size="100%">Davaadagva Damdinjav</style></author><author><style face="normal" font="default" size="100%">Otgonbaatar Urjin</style></author><author><style face="normal" font="default" size="100%">Maria Halabalaki</style></author><author><style face="normal" font="default" size="100%">Wirginia Kukula-Koch</style></author><author><style face="normal" font="default" size="100%">Daariimaa Khurelbat</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Medicinal Application of the Iceland Poppy (Papaver nudicaule L.) in Traditional Mongolian Medicine</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alkaloids</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal plant</style></keyword><keyword><style  face="normal" font="default" size="100%">Nudicaulins</style></keyword><keyword><style  face="normal" font="default" size="100%">Papaver nudicaule L.</style></keyword><keyword><style  face="normal" font="default" size="100%">Protopine</style></keyword><keyword><style  face="normal" font="default" size="100%">Traditional Mongolian medicine</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">71-76</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;In recent years, there has been a considerable focus on the utilization of natural medicinal substances, including plant-based medicines and formulations. While traditional medicine has been utilizing various medicinal plants to treat a wide range of diseases, there are still many medicinal plants and substances that have not been thoroughly studied at the scientific level. One such plant is the Iceland poppy (&lt;em&gt;Papaver nudicaule L.&lt;/em&gt;) from the Papaveraceae family. Globally, the Papaveraceae family comprises 44 genera and 760 species of which 32 species, representing 7 genera, are identified within Mongolia. The Iceland poppy (&lt;em&gt;Papaver nudicaule L.&lt;/em&gt;) is extensively distributed throughout Mongolia, with all parts of the plant, including its fruit and flowers. In addition, it has been traditionally employed in Mongolian medicine to treat a variety of ailments. However, systematic research on the practical applications and studies of the status of the local Iceland poppy in both modern and traditional Mongolian medicine remains poorly reported. Therefore, we aim to conduct a comprehensive and comparative study of the Iceland poppy (Papaver nudicaule L.) and its application in the Traditional Mongolian medicinal literature and internationally published studies. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; In this study, data was collected from a comprehensive review of the international and Traditional Mongolian medicine literature to understand the medicinal application of the Iceland poppy. Additionally, current study results were analyzed to assess its practical applications and efficacy in modern medicinal contexts. &lt;strong&gt;Results:&lt;/strong&gt; &quot;In a variant of Mongolian medicinal prescriptions, the Iceland poppy (Papaver nudicaule L.) is combined with the herb “Govo jad-5” Mongolian traditional prescription for treating surgical wounds, torn blood vessels, and both old and new wounds. Furthermore, the book 'Methods and Prescriptions for Using Medicinal Plants in Traditional Mongolian Medicine reports that Iceland poppy is part of a mixture of four types of poppies used to treat conditions such as diarrhea, intestinal inflammation, and dysentery, by boiling and administering the concoction. A study by Otgonpurev Sukhbaatar et al., (2018) determined that the optimal conditions for callus and suspension biomass production of &lt;em&gt;Papaver nudicaule L.&lt;/em&gt; are 1 mg/L naphthalene acetic acid and 0.5 mg/L benzyl adenine in MS media. Additionally, Gerelt-Od Yadamsuren et al., reported that the alkaloids 8,14-dihydroamurin, 8,14-dihydroflavinantin, and flavinantin from Papaver nudicaule L. exhibit significant antiviral activity against human rhinovirus-14. &lt;strong&gt;Conclusion: &lt;/strong&gt;Iceland poppy (&lt;em&gt;Papaver nudicaule L.&lt;/em&gt;) has been used in traditional Mongolian medical practice for a long time. it has been historically widely used in Mongolian traditional medicine to treat wounds under the name of “wound healer”. As reported by the scientific literature, the primary uses of these plants include inhibiting acetylcholinesterase enzyme, anti-cancer effects, as well as antioxidant and anti-inflammatory properties. Furthermore, regarding its chemical composition, researchers have conducted studies that confirm the presence of alkaloids in this plant, specifically isoquinoline alkaloids. These compounds are known for their diverse biological activities and potential therapeutic effects, which may contribute to the plant's traditional medicinal uses. In summary, the Iceland poppy (&lt;em&gt;Papaver nudicaule L.&lt;/em&gt;) has been utilized in traditional medicine for treating a variety of illnesses; however, it suggests that more comprehensive research is necessary to scientifically substantiate these applications.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">71</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Enkhtuul Bayarsaikhan&lt;sup&gt;1&lt;/sup&gt;, Turtushikh Damba&lt;sup&gt;1&lt;/sup&gt;, Buyanjargal Erdenebat&lt;sup&gt;1&lt;/sup&gt;, Norovnyam Ryenchinbyambaa&lt;sup&gt;1&lt;/sup&gt;, Otgonsuren Daramzav&lt;sup&gt;2&lt;/sup&gt;, Khuvitavilan Battulga&lt;sup&gt;1&lt;/sup&gt;, Munkhzul Boldbaatar&lt;sup&gt;1&lt;/sup&gt;, Myagmarsuren Badamtsetseg&lt;sup&gt;3&lt;/sup&gt;, Enkhjargal Dorjval&lt;sup&gt;1&lt;/sup&gt;, Davaadagva Damdinjav&lt;sup&gt;2&lt;/sup&gt;, Otgonbaatar Urjin&lt;sup&gt;1&lt;/sup&gt;, Maria Halabalaki&lt;sup&gt;5&lt;/sup&gt;, Wirginia Kukula-Koch&lt;sup&gt;4&lt;/sup&gt;, Daariimaa Khurelbat&lt;sup&gt;1,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Chemistry and Pharmacognosy, School of Pharmacy, Mongolian National University of Medical Sciences, Ulaanbaatar, MONGOLIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Technology, School of Pharmacy, Mongolian National University of Medical Sciences, Ulaanbaatar, MONGOLIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Clinical pharmacy and management, School of Pharmacy, Mongolian National University of Medical Sciences, Ulaanbaatar, MONGOLIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacognosy with Medicinal Plants Garden, Medical University of Lublin, POLAND. 5Department of Pharmacy, National and Kapodistrian University of Athens, Greece&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aniruddha Kulkarni</style></author><author><style face="normal" font="default" size="100%">Manoj Tare</style></author><author><style face="normal" font="default" size="100%">Meera Singh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mucuna Pruriens Seeds Extract Loaded Phytosomal Intranasal Gel for the Effective Treatment of Parkinson’s Disease</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Gel</style></keyword><keyword><style  face="normal" font="default" size="100%">L-Dopa extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Mucuna pruriens</style></keyword><keyword><style  face="normal" font="default" size="100%">Nasal gel</style></keyword><keyword><style  face="normal" font="default" size="100%">Optimization</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytosome</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">129-154</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;One phytoconstituent derived from Mucuna pruriens (legumes) is levodopa. This medication's oral usage is limited by its high first-pass metabolism and low absorption. The goal of the present research was to develop a phytosomal gel filled with levodopa extract for better delivery and brain targeting. Various techniques, including solvent evaporation, salting out anti-solvent precipitation, direct egg yolk, and egg lipids methods, were used to create phytosomal formulations. Scanning electron microscopy, particle size, x-ray diffraction, and other techniques were used to characterize phytosomes. And added into gel formation, the more successful batch was examined for several parameters. The final batch underwent a variety of animal tests, including pharmacokinetic analysis, irritation to the nasal cavity testing. The most effective phytosomes were those made via the antisolvent precipitation approach. In this investigation, a 3&lt;sup&gt;2&lt;/sup&gt;-randomized complete factorial design was employed. Batch F4 had an entrapment efficiency of 70%, a particle size of 15 (μg) and 60% CDR. The gel-formulated batch F4G3 demonstrated improved results in terms of extrudability (90.82), amount of drug (89.32%), viscosity (5421 cps at 100 rpm), and spreadability (25.18). Batch F4G3 of the Mucuna pruriens phytosome gel exhibited Higuchi's kinetics. According to the findings of the animal study, dopamine levels were significantly elevated. The pharmacokinetic and nasal irritation studies showed notable in vitro penetration of the nasal mucosa without resulting in skin irritation. For improving Parkinson's disease treatment, the phytosomal gel formulation delivered via the nasal route would be the ideal option.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">129</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Aniruddha Kulkarni&lt;sup&gt;1*&lt;/sup&gt;, Manoj Tare&lt;sup&gt;2&lt;/sup&gt;, Meera Singh&lt;sup&gt;3&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutics Sinhgad Institute of Pharmaceutical Sciences, Lonavala, Pune, 410401 INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutics, Sitabai Thite College of Pharmacy (B. Pharm), Shirur, Pune Maharashtra, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmaceutics, Sinhgad College of Pharmacy, Vadgaon (Bk), Pune, M.S. INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pallab Kar</style></author><author><style face="normal" font="default" size="100%">Ayodeji O. Oriola</style></author><author><style face="normal" font="default" size="100%">Moganavelli Singh</style></author><author><style face="normal" font="default" size="100%">Adebola O. Oyedeji</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Myricitrin-Mediated Biogenic Silver Nanoparticle Synthesis, Characterization, and its Antioxidant, Anticancer, and DNA Cleavage Activities</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anticancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">DNA cleavage</style></keyword><keyword><style  face="normal" font="default" size="100%">Myricitrin</style></keyword><keyword><style  face="normal" font="default" size="100%">Silver nanoparticles</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">121-128</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Myricitrin (MY) is a potent antioxidant flavonoid that has recently gained research interest due to its wide applications in food, cosmetics, and medicine. &lt;strong&gt;Objective: &lt;/strong&gt;The current work reports MY, its isolation and characterization from &lt;em&gt;Eugenia uniflora&lt;/em&gt; leaves, and green synthesis with AgNO&lt;sub&gt;3&lt;/sub&gt; to afford myricitrin-based silver nanoparticles (MY-Ag NPs). &lt;strong&gt;Materials and Methods: &lt;/strong&gt;The biosynthesized nanoparticles (NPs) were characterized using UV, field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), High-resolution transmission electron microscopy (HRTEM) and Dynamic light scattering (DLS) methods. Antioxidant, anti-cancer, and DNA cleavage activities were based on standard&lt;em&gt; in vitro &lt;/em&gt;bioassay methods. &lt;strong&gt;Results: &lt;/strong&gt;The UV-vis absorption peak at 430 nm suggests the formation of silver-based NPs. The FESEM imaging showed spherical-to-cubical shaped MY-Ag NPs with an average size of 45.35 nm. The EDX analysis showed the presence of elemental Ag (89.40%) and N (10.22%), suggesting a successful synthesis. The XRD analysis revealed various peaks at 38.37⁰, 43.56⁰, 63.76⁰, and 77.77⁰, which suggest metallic silver reflections, further establishing the crystallinity of NPs. The MY-Ag NPs inhibited O&lt;sub&gt;2&lt;/sub&gt; -, OH-, H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;, and NO free radicals in a dose-dependent manner. At 50 and 80 μg/mL, it demonstrated a better inhibitory effect on OH- radical than &lt;em&gt;L&lt;/em&gt;-ascorbic acid. The cytotoxicity (IC&lt;sub&gt;50&lt;/sub&gt;) against human cancer cell lines of the kidney (ACHN) and the liver (HepG2) were 54.21 ± 0.06 μg/mL and 33.36 ± 2.25 μg/mL respectively at 48 h post-treatment. Lastly, at 20 mg/mL for 120 minutes, MY-Ag NPs cleaved DNA, acting as chemical nucleases. This may suggest its capacity to impede cancer cells by cleaving the genome. &lt;strong&gt;Conclusion: &lt;/strong&gt;Therefore, this study has shown that Myricitrinbased Ag NPs possess notable antioxidant and cytotoxicity that can be further exploited in the search for newer anticancer agents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">121</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Pallab Kar&lt;sup&gt;1&lt;/sup&gt;, Ayodeji O. Oriola&lt;sup&gt;2,*&lt;/sup&gt;, Moganavelli Singh&lt;sup&gt;3&lt;/sup&gt;, Adebola O. Oyedeji&lt;sup&gt;1,2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;African Medicinal Flora and Fauna Research Niche Area, Walter Sisulu University Nelson Mandela Drive, P/Bag X1, Mthatha 5117, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemical and Physical Sciences, Walter Sisulu University, Nelson Mandela Drive, P/ Bag X1, Mthatha 5117, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Nano-Gene and Drug Delivery Group, Discipline of Biochemistry, University of KwaZulu-Natal, Private Bag, Durban X54001, SOUTH AFRICA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pallab Kar</style></author><author><style face="normal" font="default" size="100%">Ayodeji O. Oriola</style></author><author><style face="normal" font="default" size="100%">Adebola O. Oyedeji</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Natural Flavonoid Glycoside-Based Zinc Oxide Nanoparticles: Compound Isolation, Nanoparticle Green Synthesis, Characterization, and in vitro Antioxidant, Anti-hyperglycaemic and Anti-inflammatory Effects</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammation</style></keyword><keyword><style  face="normal" font="default" size="100%">antihyperglycaemia</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Green synthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">natural flavonoid glycosides</style></keyword><keyword><style  face="normal" font="default" size="100%">ZnO Nanoparticles</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">531-541</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Recent advances in effective and efficient drug delivery have favoured the biological applications of phytochemical-based metal oxide nanoparticles (NPs). Objective: This study, therefore, utilized a flavonoid glycoside, Myricitrin (MY), isolated from &lt;em&gt;Eugenia uniflora &lt;/em&gt;as a biogenic substance for the synthesis of zinc oxide nanoparticles (ZnONPs) and evaluated the antioxidant, anti-hyperglycaemic, and anti-inflammatory potentials. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Flavonoid glycoside was isolated from the leaf of &lt;em&gt;E. uniflora&lt;/em&gt; following standard phytochemical techniques for extraction, solvent-partitioning, column chromatography, and thin-layer chromatography. The phytocompound was characterized by NMR and HRESI-MS methods. Zinc oxide NPs were green synthesized using the isolated flavonoid glycoside. The biogenic ZnONPs were characterized using UV-Vis, FESEM, EDX, and XRD techniques. The biological potential of the MY-ZnONPs was based on in vitro analysis. Nitric oxide (NO), H2O2, OH, and O2 - antioxidant methods were used. The anti-hyperglycaemic effect was based on α-amylase and α-glucosidase enzyme inhibition, while the egg albumin denaturation (EAD) method was used to determine the antiinflammatory effect. &lt;strong&gt;Results:&lt;/strong&gt; Flavonoid glycoside was isolated and characterized as myricitrin from &lt;em&gt;E. uniflora&lt;/em&gt;. The MY-ZnONPs were green synthesized as a greyish powder. The UV-Vis absorption peaks at 387 and 415 nm match the characteristic peaks for ZnONPs. The FESEM revealed petal-, irregular-, and spindle-shaped NPs of 30-80 nm size, which tend to agglomerate in clusters and bundles. The EDX analysis showed the elemental weight percentage of Zn and O to be 79.83% and 18.51%, respectively, indicating the successful formation of ZnO nanoparticles. The X-ray diffractogram showed the crystallinity of the NPs at 29.23⁰, 36.25⁰, 51.50⁰, 63.67⁰, 72.06⁰, and 78.90⁰. At 100 μg/mL, the NPs demonstrated a comparable 68% inhibition of O&lt;sub&gt;2&lt;/sub&gt; - to Quercetin, the standard antioxidant. They inhibited EAD in a dose-de pendent manner, having ≥75% inhibition at 200 μg/mL. Finally, they exhibited notable anti-hyperglycaemic properties against α-amylase and α-glucosidase with IC&lt;sub&gt;50&lt;/sub&gt; of 89.24±0.63 and 105.95±0.05 μg/mL, respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; This study has shown MY-ZnONPs as a flavonoid glycoside-based metal oxide nanoparticle with notable antioxidant, anti-diabetic, and anti-inflammatory activities.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">531</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Pallab Kar&lt;sup&gt;1,*&lt;/sup&gt;, Ayodeji O. Oriola&lt;sup&gt;2,*&lt;/sup&gt;, Adebola O. Oyedeji&lt;sup&gt;1,2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;African Medicinal Flora and Fauna Research Niche Area, Walter Sisulu University Nelson Mandela Drive, P/Bag X1, Mthatha 5117, SOUTH AFRICA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemical and Physical Sciences, Walter Sisulu University, Nelson Mandela Drive, P/ Bag X1, Mthatha 5117, SOUTH AFRICA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Patcharin Singdam</style></author><author><style face="normal" font="default" size="100%">Anussara Kamnate</style></author><author><style face="normal" font="default" size="100%">On-Anong Somsap</style></author><author><style face="normal" font="default" size="100%">Ruhainee Tohkayomatee</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Screening, Antioxidant Potential, and α-Glucosidase Inhibition of Causonis trifolia Leaf Extracts: A Solvent-Based Comparative Study</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antidiabetic</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Causonis trifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">α-glucosidase</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">164-170</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Medicinal plants are used in diabetes mellitus due to their proven minimal adverse effects in humans. &lt;em&gt;Causonis trifolia&lt;/em&gt; leaves have been used as traditional medicine for various treatments. &lt;strong&gt;Objective:&lt;/strong&gt; The aim of this research was to investigate the phytochemicals, the total flavonoid and phenolic content, and in-vitro antioxidant and antidiabetic activities of the extracts of &lt;em&gt;C. trifolia &lt;/em&gt;leaves. &lt;strong&gt;Method:&lt;/strong&gt; The leaves of &lt;em&gt;C. trifolia&lt;/em&gt; were sequentially extracted with maceration in hexane, ethyl acetate, ethanol, and 50% ethanol. Then, the &lt;em&gt;C. trifolia&lt;/em&gt; leaf extracts were assessed for antioxidant activity by the DPPH and ABTS radical scavenging and FRAP assay. Total phenolic and flavonoid contents were determined by the Folin- Ciocalteu and aluminum chloride colorimetric methods, respectively. Antidiabetic activity was evaluated by determination of α-glucosidase inhibitory effect. &lt;strong&gt;Results:&lt;/strong&gt; Preliminary phytochemical analysis of ethanol and 50% ethanol extracts of &lt;em&gt;C. trifolia&lt;/em&gt; leaves showed positive results for alkaloids, coumarin, tannins, saponins, cardiac glycosides, terpenoids, and steroids. The 50% ethanol extract had the best antioxidant activities of the three antioxidant assays (&lt;em&gt;p&lt;/em&gt; &amp;lt; 0.05). The results revealed higher phenolic and flavonoid contents in 50% ethanol extract than in the other extracts (p &amp;lt; 0.05). Moreover, the 50% ethanol extract exhibited the best potential as α-glucosidase inhibitors of all the extracts and acarbose (&lt;em&gt;p &lt;/em&gt;&amp;lt; 0.05). &lt;strong&gt;Conclusions:&lt;/strong&gt; The results conclude that the &lt;em&gt;C. trifolia&lt;/em&gt; leaves with 50% ethanol as the solvent possessed the potential to extract the highest levels of phytochemical content and have potential antioxidant and α-glucosidase inhibitory activities for diabetic therapy.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">164</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Patcharin Singdam&lt;sup&gt;1*&lt;/sup&gt;, Anussara Kamnate&lt;sup&gt;2&lt;/sup&gt;, On-Anong Somsap&lt;sup&gt;3&lt;/sup&gt;, Ruhainee Tohkayomatee&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Anatomy, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biochemistry, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Anchana Babu</style></author><author><style face="normal" font="default" size="100%">Rekha D Kini</style></author><author><style face="normal" font="default" size="100%">Nayanatara Arun Kumar</style></author><author><style face="normal" font="default" size="100%">Megha Gokul</style></author><author><style face="normal" font="default" size="100%">Bhagyalakshmi K</style></author><author><style face="normal" font="default" size="100%">Sneha Shetty B</style></author><author><style face="normal" font="default" size="100%">Vinodini NA</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Potential Role of Ashwagandha [Withania Somnifera] As An Antioxidant On Aluminium Chloride-Induced Testicular Damage In Wistar Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Malondialdehyde</style></keyword><keyword><style  face="normal" font="default" size="100%">Reactive Oxygen Species</style></keyword><keyword><style  face="normal" font="default" size="100%">Reduced glutathione</style></keyword><keyword><style  face="normal" font="default" size="100%">Sperm morphology</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">583-587</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Aluminium is most prevalent and third most abundant element in earth crust after oxygen. Its exposure in high concentration can accumulate in many organs that damage various organs in living organisms like humans and animals. Although aluminum (Al) is known to induce oxidative damage through various mechanisms including binding to negatively charged phospholipids on the membrane of various tissue cell which are rich in PUFA.Hence,this study was aimed to find the potential role of ashwagandha on aluminum induced testicular toxicity. &lt;strong&gt;Methods: &lt;/strong&gt;Animals were segregated into 4 groups of 6 rats in each. The control group, the Ashwagandha treated group, the Aluminum intoxicated group, pretreated with Ashwagandha with Aluminum intoxicity group. Testicular tissue was removed and were stored in 10% formalin saline and histopathological slides were done . A part of the tissues were processed for estimation of MDA and GSH level. &lt;strong&gt;Results: &lt;/strong&gt;In the present study administration of aluminum in rats showed a significant decrease in the testicular tissue level of GSH and sperm count, as well as increase in the level of MDA and sperm morphology in aluminum treated group compared to normal control. Treatment with Ashwagandha showed a significant increase in testicular GSH level, sperm count and decrease in MDA level sperm morphology. &lt;strong&gt;Conclusion:&lt;/strong&gt; The results of this study revealed that oral Aluminum Chloride administration induced adverse oxidative effects on the exposed animals and treatment with&lt;em&gt; W. somnifera &lt;/em&gt;reduced the extent of aluminium chloride-induced tissue injury&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">583</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Anchana Babu&lt;sup&gt;1&lt;/sup&gt;, Rekha D Kini&lt;sup&gt;1*&lt;/sup&gt;, Nayanatara Arun Kumar&lt;sup&gt;1&lt;/sup&gt;, Megha Gokul&lt;sup&gt;1&lt;/sup&gt;, Bhagyalakshmi K&lt;sup&gt;1&lt;/sup&gt;, Sneha Shetty B&lt;sup&gt;1&lt;/sup&gt;, Vinodini NA&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Physiology, Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, India&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amina DOUBBI BOUNOUA</style></author><author><style face="normal" font="default" size="100%">Mokhtaria Yasmina BOUFADI</style></author><author><style face="normal" font="default" size="100%">Karima BOUGUEROUA</style></author><author><style face="normal" font="default" size="100%">Soumia KEDDARI</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Preparation, Characterization and Wound Healing Effect of β Chitosan and Gelatin Hydrogels from Sepia Officinalis: In Vivo Study</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Gelatin</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydrogel</style></keyword><keyword><style  face="normal" font="default" size="100%">Os</style></keyword><keyword><style  face="normal" font="default" size="100%">Sepia Officinalis</style></keyword><keyword><style  face="normal" font="default" size="100%">Skin</style></keyword><keyword><style  face="normal" font="default" size="100%">Wound Healing</style></keyword><keyword><style  face="normal" font="default" size="100%">β Chitosan</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">244-251</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Wound healing is a fundamental process through which the body repairs itself following damage to the skin's integrity. This process is intricate and involves multiple biological mechanisms. The objective of this study is to assess the wound healing properties of β-chitosan and gelatin hydrogels. Twenty-five rats were divided into five groups to facilitate the evaluation of wound closure rates and histopathological changes. Upon analyzing the results, we noted a decrease in the initial surface area of all wounds examined. The extent of contraction varied depending on the type of hydrogel used. By day 14, the contraction was most significant in the hydrogel (ch + gel) group (97.30%), followed closely by β-chitosan (96.72%) and gelatin (96.63%), as well as the cicatryl-bio treatment (92.76%).&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">244</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Amina DOUBBI BOUNOUA&lt;sup&gt;1&lt;/sup&gt;, Mokhtaria Yasmina BOUFADI&lt;sup&gt;1,2,3*&lt;/sup&gt;, Karima BOUGUEROUA&lt;sup&gt;1&lt;/sup&gt;, Soumia KEDDARI&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Laboratory of Bioeconomics, Food Safety and Health, Faculty of Natural Sciences and Life, University of Abdelhamid Ibn Badis, Mostaganem 27000, ALGERIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of biology, University of Houari Boumediene USTHB Algiers 16000, ALGERIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Laboratory of Pharmaceutical Chemistry, Faculty of Pharmacy, Libre university of Brussels, 1050 Brussels, BELGIUM.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Paresh G. Koli</style></author><author><style face="normal" font="default" size="100%">Yashashri Shetty</style></author><author><style face="normal" font="default" size="100%">Reetu Sharma</style></author><author><style face="normal" font="default" size="100%">Bal Krishan Sevatkar</style></author><author><style face="normal" font="default" size="100%">Anaya A. Pathrikar</style></author><author><style face="normal" font="default" size="100%">Hemant S. Paradkar</style></author><author><style face="normal" font="default" size="100%">Mukesh B Chawda</style></author><author><style face="normal" font="default" size="100%">Sangam S. Narvekar</style></author><author><style face="normal" font="default" size="100%">Megha L. Nalawade</style></author><author><style face="normal" font="default" size="100%">Pawankumar R. Godatwar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Prospective, Multi-centre, Open label, Single arm Study to Evaluate the Efficacy and Safety of Amlapitta Mishran Suspension in Participants with Amlapitta (Symptomatic Gastritis)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ayurveda</style></keyword><keyword><style  face="normal" font="default" size="100%">Gastritis</style></keyword><keyword><style  face="normal" font="default" size="100%">Symptom scores</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">545-551</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;The multi-center clinical study was conducted to revalidate the efficacy and safety of Amlapitta Mishran Suspension in Amlapitta (symptomatic gastritis) in a larger sample size in improving Amlapitta Symptom Rating Scale Score, PPDS score, EPS score, and safety. &lt;strong&gt;Methods: &lt;/strong&gt;The study was a multi-centric, open-labeled, single-arm, prospective clinical trial in participants with Amlapitta (symptomatic gastritis). Participants with the presence of Amlapitta (symptomatic gastritis), as diagnosed by the Amlapitta Symptom Rating Scale Score ≥ 5 were included in the study. Participants were advised to take Amlapitta Mishran Suspension in a dose of 15 ml twice daily for 14 days. The study involved three visits. The investigator recorded the Amlapitta Symptom Rating Scale (ASRS) Score, Post Prandial Distress Syndrome (PPDS) Score, and Epigastric Pain Syndrome (EPS) Score at screening visit (Visit 1), baseline visit (Visit 2) and final visit (Visit 3). The p&amp;lt;0.05 was considered statistically significant measured by paired t-test or Wilcoxon Signed Rank test. &lt;strong&gt;Results: &lt;/strong&gt;In the multi-center study 204 participants completed the study. At final visit, a statistically significant (p&amp;lt;0.001) reduction was reported in mean Total ASRS score, PPDS score, and EPS score as compared to the baseline scores. The individual ASRS, PPDS, and EPS variables also exhibited significant reduction (p&amp;lt;0.001) at the final visit. None of the participants reported any adverse events during the study. &lt;strong&gt;Conclusion: &lt;/strong&gt;Amlapitta Mishran Suspension treatment for 14 days effectively and safely reduced the clinical symptoms of Amlapitta (symptomatic gastritis) assessed by Amlapitta Symptom Rating Scale, Postprandial Distress Syndrome and Epigastric Pain Syndrome scores.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">545</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Paresh G. Koli&lt;sup&gt;1*,&lt;/sup&gt; Yashashri Shetty&lt;sup&gt;1&lt;/sup&gt;, Reetu Sharma&lt;sup&gt;2&lt;/sup&gt;, Bal Krishan Sevatkar&lt;sup&gt;2&lt;/sup&gt;, Anaya A. Pathrikar&lt;sup&gt;3&lt;/sup&gt;, Hemant S. Paradkar&lt;sup&gt;3&lt;/sup&gt;, Mukesh B Chawda&lt;sup&gt;4&lt;/sup&gt;, Sangam S. Narvekar&lt;sup&gt;5&lt;/sup&gt;, Megha L. Nalawade&lt;sup&gt;6&lt;/sup&gt;, Pawankumar R. Godatwar&lt;sup&gt;7&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology and Therapeutics, Seth GS Medical College and KEM Hospital, Mumbai. INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Roga Nidana Evum Vikriti Vigyana, National Institute of Ayurveda, Madhav Vilas Palace, Jorawar Singh Gate Amer Road, Jaipur - 302 002. INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Kayachikitsa, Ayurvidya Prasarak Mandal’s, Seth R.V. Ayurvedic Hospital, Sion (E), Mumbai - 400 022. INDIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Medical Services, Solumiks Herbaceuticals Limited, 135, Nanubhai Desai Road, Khetwadi, Mumbai - 400 004. INDIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Medical Services, Shree Dhootapapeshwar Limited, 135, Nanubhai Desai Road, Khetwadi, Mumbai – 400 004. INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Shree Dhootapapeshwar Limited, 135, Nanubhai Desai Road, Khetwadi, Mumbai - 400 004. INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Roga Nidana Evum Vikriti Vigyana, National Institute of Ayurveda, Madhav Vilas Palace, Jorawar Singh Gate, Amer Road Jaipur - 302 002. INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Durga Prasad Kondeti</style></author><author><style face="normal" font="default" size="100%">T. Sundarrajan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Review on Chemical Profile and Pharmacological Properties of Marine Sponge Tectitethya Crypta</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anticancer drugs</style></keyword><keyword><style  face="normal" font="default" size="100%">Antiviral drugs</style></keyword><keyword><style  face="normal" font="default" size="100%">Bioactive compounds</style></keyword><keyword><style  face="normal" font="default" size="100%">Marine sponges</style></keyword><keyword><style  face="normal" font="default" size="100%">pharmacological properties</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">608-619</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Marine sponges have gained recognition as a valuable resource due to their significant pharmacological properties. The investigation of substances produced by sponges has been extensively researched to identify their pharmacological properties. Marine sponges, which are part of the phylum Porifera, are thought to be the main source of marine natural products. Sponges are multicellular organisms that have a number of pores and channels for exchanging water; the secondary metabolites they create are in turn influenced by their specific environmental circumstances. Natural products such as lipids, terpenoids, peptides, alkaloids, and steroids are abundant in the marine sponge genus Tectitethya crypta. These compounds have unique chemical structures and have shown promising biological activities, making them ideal candidates for the development of novel drugs to treat various ailments. Tectitethya crypta is a sessile filter-feeder that produces a variety of bioactive compounds, including nucleosides and other secondary metabolites. This article reviews the biology and chemistry of Tectitethya crypta and serves as an introduction to the organism. We discuss the taxonomic classification, morphology, and microenvironment of the sponge, as well as the chemical structures and biological activities of its bioactive compounds. Tectitethya crypta was the source for the development of vidarabine, ara-C, and gemcitabine, which are used to treat viruses and cancer, respectively. We discussed about how these molecules may be used to treat parasitic and infectious disorders.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">608</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Durga Prasad Kondeti&lt;sup&gt;1&lt;/sup&gt;, T. Sundarrajan&lt;sup&gt;1*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Chemistry, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prajna R H</style></author><author><style face="normal" font="default" size="100%">Shivananda Nayak</style></author><author><style face="normal" font="default" size="100%">Priya V</style></author><author><style face="normal" font="default" size="100%">Shruthi Rai P</style></author><author><style face="normal" font="default" size="100%">Shivaraja shankara Y M</style></author><author><style face="normal" font="default" size="100%">Prashanthkumar Goudappala</style></author><author><style face="normal" font="default" size="100%">Dinesh PV</style></author><author><style face="normal" font="default" size="100%">Namratha KG</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The role of TNF-Alpha, IL-6, Adiponectin, and Leptin in Inflammation and Metabolic Dysregulation in Type 2 Diabetes Mellitus</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adiponectin</style></keyword><keyword><style  face="normal" font="default" size="100%">IL-6</style></keyword><keyword><style  face="normal" font="default" size="100%">Inflammation</style></keyword><keyword><style  face="normal" font="default" size="100%">Leptin</style></keyword><keyword><style  face="normal" font="default" size="100%">Metabolic Dysregulation</style></keyword><keyword><style  face="normal" font="default" size="100%">TNF-Alpha</style></keyword><keyword><style  face="normal" font="default" size="100%">Type 2 diabetes mellitus</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">699-702</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Type 2 Diabetes Mellitus (T2DM) is characterized by chronic inflammation and metabolic dysregulation. The present study investigates the role of inflammatory markers, including TNF-alpha and IL-6, and metabolic hormones such as adiponectin and leptin, in individuals with T2DM. &lt;strong&gt;Methods:&lt;/strong&gt; A total of 147 participants diagnosed with T2DM were included in the study. Clinical and biochemical parameters, including fasting blood sugar (FBS), glycated hemoglobin (HbA1C), adiponectin, leptin, TNF-alpha, and IL-6, were measured. Descriptive statistics and correlation analysis were performed to determine associations between inflammatory markers and metabolic dysregulation.&lt;strong&gt; Results: &lt;/strong&gt;The mean age of participants was &lt;strong&gt;42.63 ± 6.38 &lt;/strong&gt;years, and the average BMI was &lt;strong&gt;28.38 ± 2.25 kg/m²&lt;/strong&gt;. FBS and HbA1C levels were &lt;strong&gt;175.72 ± 61.61 mg/dL&lt;/strong&gt; and &lt;strong&gt;7.26 ± 0.94%,&lt;/strong&gt; respectively. The mean adiponectin and leptin levels were &lt;strong&gt;4.71 ± 1.75 μg/mL&lt;/strong&gt; and &lt;strong&gt;20.58 ± 5.19 ng/mL&lt;/strong&gt;, respectively. TNF-alpha and IL-6 levels averaged &lt;strong&gt;132.00 ± 9.45 pg/mL&lt;/strong&gt; and &lt;strong&gt;33.52 ± 14.55 pg/mL&lt;/strong&gt;, respectively. Correlation analysis indicated an inverse relationship between adiponectin and BMI, while leptin was positively correlated with BMI and insulin levels. Elevated TNFalpha and IL-6 levels were associated with increased HbA1C and fasting blood glucose. &lt;strong&gt;Conclusion: &lt;/strong&gt;This study highlights the significant role of inflammatory markers in metabolic dysregulation among T2DM patients. Elevated TNF-alpha and IL-6 levels reinforce the link between chronic inflammation and impaired glucose metabolism. These findings underscore the need for anti-inflammatory strategies in diabetes management.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">699</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Prajna R H&lt;sup&gt;1,2&lt;/sup&gt;, Shivananda Nayak&lt;sup&gt;3&lt;/sup&gt;, Priya V&lt;sup&gt;4*&lt;/sup&gt;, Shruthi Rai P&lt;sup&gt;5&lt;/sup&gt;, Shivaraja shankara Y M&lt;sup&gt;6&lt;/sup&gt;, Prashanthkumar Goudappala&lt;sup&gt;7&lt;/sup&gt;, Dinesh PV&lt;sup&gt;8&lt;/sup&gt;, Namratha KG&lt;sup&gt;9&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Research scholar, SaveethaResearch Center, Saveetha Institute of Medical and Technical Sciences(SIMATS), Chennai, INDIA,600077&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Assistant Professor, Department of Biochemistry, KVG Medical College and Hospital, Sullia, INDIA, 574327&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Professor, Department of Biochemistry, Subbaiah Institute of Medical Science, Shivamogga, INDIA,577222&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Professor, Center of Molecular Medicine and Diagnostics (COMManD), Department of Biochemistry, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University Chennai, INDIA,600077&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Professor, Department of Biochemistry, KVG Medical College and Hospital, Sullia, INDIA, 574327&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Professor, Department of Biochemistry, KVG Medical College and Hospital, Sullia, INDIA, 574327&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Associate Professor, Department of Biochemistry, Sri Siddhartha Medical College, Sri Siddhartha Academy of Higher Education, Tumkur, INDIA ,572107&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Professor, Department of Community medicine, KVG Medical College and Hospital, Sullia, INDIA, 574327&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Professor, Department of Microbiology, KVG Medical College and Hospital,Sullia , INDIA, 574327.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amaresh Parimi</style></author><author><style face="normal" font="default" size="100%">Silambarasan K</style></author><author><style face="normal" font="default" size="100%">Prashantkumar Goudappala</style></author><author><style face="normal" font="default" size="100%">Ravi Mundugaru</style></author><author><style face="normal" font="default" size="100%">Parameswari Royapuram Parthasarathy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synergistic antioxidant and antidiabetic activities of Tinospora cordifolia and Azadirachta indica extracts supported by in-silico molecular docking and ADMET evaluation</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidants</style></keyword><keyword><style  face="normal" font="default" size="100%">Azadirachta indica</style></keyword><keyword><style  face="normal" font="default" size="100%">Health</style></keyword><keyword><style  face="normal" font="default" size="100%">Plants</style></keyword><keyword><style  face="normal" font="default" size="100%">PTP1B</style></keyword><keyword><style  face="normal" font="default" size="100%">Tinospora cordifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">α-amylase</style></keyword><keyword><style  face="normal" font="default" size="100%">α-glucosidase</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">310-321</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Type 2 Diabetes mellitus is a chronic metabolic disorder which worsens by increased oxidative stress resulting in other diabetes associated complications. Tinospora cordifolia (TC) and &lt;em&gt;Azadirachta indica&lt;/em&gt; (AI) are traditional medicinal plants that has been used for diabetes since ancient times, but their combined potential as a formulation has not been evaluated for the management of diabetes. &lt;strong&gt;Objectives:&lt;/strong&gt; This study aimed to profile the phytochemical composition of 70% hydroethanolic extracts of TC and AI, assess their antioxidant and antidiabetic activity individually and in combination, and further substantiate their efficacy through in-silico molecular docking and ADMET evaluation of their key bioactive compounds, berberine and nimbolide. &lt;strong&gt;Methods: &lt;/strong&gt;Hydroethanolic extracts of TC and AI were subjected to preliminary phytochemical screening, quantification of primary and secondary metabolites, and HPTLC profiling. Five combinations of TC:AI (1:1, 1:2, 2:1, 1:3, 3:1) were prepared and evaluated for antioxidant activity using DPPH, ABTS, and FRAP assays, and for antidiabetic potential using α-amylase, α-glucosidase, and PTP1B inhibition assays. IC&lt;sub&gt;₅₀&lt;/sub&gt; values were calculated. &lt;em&gt;In-silico&lt;/em&gt; studies were performed for berberine and nimbolide using AutoDock 4.2.6 against PPARγ, GLUT4, and IRS1. Drug-likeness and ADMET properties were predicted using SwissADME and pkCSM. &lt;strong&gt;Results:&lt;/strong&gt; Phytochemical profiling confirmed the presence of alkaloids, polyphenols, flavonoids, and tannins. TC demonstrated stronger inherent antioxidant and antidiabetic activity than AI. Among combinations, 1:1 and 3:1 formulations showed the highest potency with IC₅₀ values comparable to standards. Molecular docking revealed strong binding affinities of berberine and nimbolide toward PPARγ, GLUT4, and IRS1, while ADMET prediction indicated acceptable pharmacokinetic behaviour and good drug-likeness. &lt;strong&gt;Conclusion:&lt;/strong&gt; The TC:AI 1:1 formulation exhibited synergistic antioxidant and antidiabetic effects, supported by favorable &lt;em&gt;in-silico&lt;/em&gt; interactions and pharmacokinetic profiles, highlighting its potential as a natural therapeutic option for T2DM management.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">310</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Amaresh Parimi&lt;sup&gt;1,2&lt;/sup&gt;, Silambarasan K&lt;sup&gt;3&lt;/sup&gt;, Prashantkumar Goudappala&lt;sup&gt;4&lt;/sup&gt;, Ravi Mundugaru&lt;sup&gt;5&lt;/sup&gt;, Parameswari Royapuram Parthasarathy&lt;sup&gt;3*&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Saveetha Medical College and Hospital, Saveetha Institute of Medical and Technical Sciences (SIMATS), Chennai–602105, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology, Navodaya Medical College hospital and Research Centre, Raichur Karnataka, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Molecular Biochemistry Lab, Department of Biochemistry, Saveetha Medical College and Hospital, Saveetha Institute of Medical and Technical Sciences (SIMATS), Chennai–602105, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biochemistry, Sri Siddhartha Medical College, Sri Siddhartha Academy of Higher Education, Tumkur–572107, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Pharmacology, Adichunchangari Institute of Medical Sciences, B.G Nagar Mandya Karnataka, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ayodeji O. Oriola</style></author><author><style face="normal" font="default" size="100%">Pallab Kar</style></author><author><style face="normal" font="default" size="100%">Adebola O. Oyedeji</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and Characterization of Biogenic Silver Nanoparticles using Medicinally important Nigella sativa L. (black Cumin) and their Antioxidant, Anti‑inflammatory, and DNA Cleavage Potentials</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">DNA cleavage</style></keyword><keyword><style  face="normal" font="default" size="100%">Nigella sativa</style></keyword><keyword><style  face="normal" font="default" size="100%">Silver nanoparticles</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">282-288</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;The application of nanotechnology in herbal medicine offers promising prospects for drug delivery by enabling targeted, controlled, and efficient delivery of medicinal ingredients, potentially minimizing side effects and improving treatment outcomes. Nigella sativa L. (black Cumin) seed infusions are useful in Asian and African ethnomedicines in remedying stress and inflammatory-related ailments. &lt;strong&gt;Objective: &lt;/strong&gt;On this premise, black Cumin-based silver nanoparticles (BC-Ag NP) were developed and evaluated for their biological potential. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Silver nanoparticles (AgNPs) were green synthesized using the seed aqueous extract of black cumin (BC). The BC-AgNPs were characterized using scanning electron microscopy (SEM), field emission scanning electron microscopy (FESEM), highresolution transmission electron microscopy analysis (HRTEM), energy-dispersive X-ray spectroscopy (EDX), and X-ray diffraction (XRD). The biological potential of the NPs was based on NO, H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;, •OH, and O&lt;sub&gt;2&lt;/sub&gt; •– radical scavenging antioxidant, egg albumin denaturation (anti-inflammatory), and DNA cleavage assay methods.&lt;strong&gt; Results: &lt;/strong&gt;The SEM and FESEM revealed spherical-to-cubical-shaped ultrafine BC-Ag NPs with a size of less than 100 nm. The HR-TEM micrograph confirmed each NP to be spherical in shape and within the 10-50 nm range. The X-ray diffractogram showed the crystallinity of the NPs with a sharp peak at 38.12° [reflection index (111)] at an average size of 47 nm. The transformation of metallic silver into elemental silver was validated by EDX analysis, with 97.58% elemental Ag at ~3 keV acute curve. The BC-Ag NPs showed dose-dependent antioxidant activity, with IC50 of 87.56 ± 1.54 and 110.5 ± 2.27 μg/mL against H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; and O&lt;sub&gt;2&lt;/sub&gt; ._ free radicals, respectively. The anti-inflammatory activity of the NPs was one-third the potency of Diclofenac sodium (standard drug) at IC&lt;sub&gt;50&lt;/sub&gt; of 103.44 ± 5.35 μg/mL. Finally, the BC-Ag NPs acted as chemical nucleases to cleave DNA at a 20 mg/mL concentration for 120 minutes.&lt;strong&gt; Conclusion: &lt;/strong&gt;This study has shown that AgNPs biosynthesized with black Cumin seed extract possess notable antioxidant, anti-inflammatory, and DNA cleavage properties and, thus, may be a useful nanomaterial for efficient pharmaceutical delivery.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">282</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ayodeji O. Oriola&lt;sup&gt;1,*&lt;/sup&gt;, Pallab Kar&lt;sup&gt;2,*&lt;/sup&gt;, Adebola O. Oyedeji&lt;sup&gt;1,2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemical and Physical Sciences, Walter Sisulu University, Nelson Mandela Drive, P/ Bag X1, Mthatha 5117, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;African Medicinal Flora and Fauna Research Niche Area, Walter Sisulu University Nelson Mandela Drive, P/Bag X1, Mthatha 5117, SOUTH AFRICA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pallab Kar</style></author><author><style face="normal" font="default" size="100%">Ayodeji O. Oriola</style></author><author><style face="normal" font="default" size="100%">Adebola O. Oyedeji</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and Characterization of Biogenic Zinc Oxide Nanoparticles Using Eugenia uniflora Extract and its Anticancer Potential</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anticancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Eugenia uniflora</style></keyword><keyword><style  face="normal" font="default" size="100%">Green synthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">ZnO Nanoparticles</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">506-510</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Green synthesized nanoparticles have continued to be an important bioresource, exhibiting targeted delivery to diseases’ active sites with considerable eco-friendliness and effectiveness. &lt;strong&gt;Objective:&lt;/strong&gt; In this study, the medicinally useful Eugenia uniflora L. through green synthesis with zinc oxide nanoparticles (ZnONPs), was potentiated for its anticancer activity. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;The leaf aqueous extract of E. uniflora (EU) was biosynthesized with zinc acetate dihydrate precursor to develop EU-ZnONPs. Characterization was based on field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), ultraviolet-visible (UV-Vis) spectroscopy, and energy-dispersive X-ray (EDX) spectroscopy. The anticancer potential of EU-ZnONPs was based on MTT-based cytotoxicity (CC50) against human cancerous (HepG2 and ACHN) cell lines. &lt;strong&gt;Results:&lt;/strong&gt; The FESEM revealed spherical-to-cubical shaped EU-ZnONPs with 40 and 80 nm average size ranges. Further microscopic evaluation by HRTEM showed that the bulk of the nanoparticles (NPs) are spherical, ranging from 5–30 nm in size. The UV-Vis absorption peak at 387 nm agreed with the characteristic 300-400 nm peak range of biogenic ZnONPs. The presence of Zn and O at elemental weight percentages of 73.55 and 23.05% confirmed the successful green synthesis of the Eu-ZnONPs. At 48 h post-treatment, the cytotoxicity against HepG2 and ACHN cancer cell lines was concentration-dependent, with CC50 values of 54.21 ± 0.06 μg/mL and 33.36 ± 2.25 μg/mL, respectively. &lt;strong&gt;Conclusion: &lt;/strong&gt;This study has shown that EUZnONPs possess notable cytotoxicity against HepG2 and ACHN cancer cells, thus suggesting E. uniflora extract-based ZnONPs as a promising anticancer bioresource.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">506</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Pallab Kar&lt;sup&gt;1*&lt;/sup&gt;, Ayodeji O. Oriola&lt;sup&gt;2*&lt;/sup&gt;, Adebola O. Oyedeji&lt;sup&gt;1,2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;African Medicinal Flora and Fauna Research Niche Area, Walter Sisulu University, Nelson Mandela Drive, P/Bag X1, Mthatha 5117, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemical and Physical Sciences, Walter Sisulu University, Nelson Mandela Drive, P/ Bag X1, Mthatha 5117, SOUTH AFRICA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amruth Kiran</style></author><author><style face="normal" font="default" size="100%">Praveen Kumar S E</style></author><author><style face="normal" font="default" size="100%">Devasrita Dash</style></author><author><style face="normal" font="default" size="100%">Govindasamy Suresh</style></author><author><style face="normal" font="default" size="100%">Vasudev R Pai</style></author><author><style face="normal" font="default" size="100%">Arul Amuthan</style></author><author><style face="normal" font="default" size="100%">K Ganesh Shenoy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Tribulus terrestris: A Revisit to a Promising Herbal Diuretic</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">diuresis</style></keyword><keyword><style  face="normal" font="default" size="100%">diuretic agent</style></keyword><keyword><style  face="normal" font="default" size="100%">Herbal medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Indian traditional medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Siddha system of medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Tribulus terrestris</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">653-661</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Standard diuretics are essential for managing fluid as well as electrolyte overload and hypertension but are frequently associated with adverse effects such as electrolyte imbalances, renal dysfunction, and metabolic disturbances. This has prompted increased interest in safer, plant-based alternatives. &lt;em&gt;Tribulus terrestris&lt;/em&gt;, a medicinal herb used as a diuretic agent in traditional systems, has shown promising diuretic activity in recent experimental studies. &lt;strong&gt;Objective: &lt;/strong&gt;To provide an outline and assess the reported diuretic effects of &lt;em&gt;Tribulus terrestris&lt;/em&gt;, including its phytochemical profile, mechanisms of action, and findings from in vivo, in vitro, and in silico studies. &lt;strong&gt;Methods: &lt;/strong&gt;An extensive literature survey was performed on the PubMed, Scopus, ScienceDirect, and Google Scholar databases for studies published between 2000 and 2025. The inclusion criterion was original articles evaluating the diuretic activity of &lt;em&gt;Tribulus terrestris&lt;/em&gt;. Articles without diuretic activity were excluded. Data extraction included the plant part used, extract type, dosage, model used and observed effects. &lt;strong&gt;Results: &lt;/strong&gt;This review highlights the diuretic properties and phytoconstituents of &lt;em&gt;Tribulus terrestris&lt;/em&gt;. Most studies have used aqueous or ethanolic extracts of fruits or whole plants and reported significant increases in urine output and urinary sodium excretion, which are often comparable to those of standard diuretics such as furosemide. &lt;strong&gt;Conclusion: &lt;/strong&gt;This review highlights the preclinical diuretic activity of &lt;em&gt;Tribulus terrestris&lt;/em&gt;. It has shown effective and welltolerated diuretic potential in preclinical and human subjects. It is a promising, likely herbal-based diuretic, natural alternative or complement, adjunct to conventional diuretics, which warrants further investigation through clinical studies.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">653</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Amruth Kiran&lt;sup&gt;1&lt;/sup&gt;, Praveen Kumar S E&lt;sup&gt;2&lt;/sup&gt;, Devasrita Dash&lt;sup&gt;1&lt;/sup&gt;, Govindasamy Suresh&lt;sup&gt;1&lt;/sup&gt;, Vasudev R Pai&lt;sup&gt;3&lt;/sup&gt;, Arul Amuthan&lt;sup&gt;1,4*&lt;/sup&gt;, K Ganesh Shenoy&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Basic Medical Sciences, Manipal Academy of Higher Education, Manipal, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology, Manipal Tata Medical College, Manipal Academy of Higher Education, Manipal, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacognosy, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Coordinator, Division of Siddha, Centre for Integrative Medicine and Research (CIMR), Manipal Academy of Higher Education, Manipal, Karnataka, India&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ayodeji Oluwabunmi Oriola</style></author><author><style face="normal" font="default" size="100%">Pallab Kar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Zinc Oxide Nanoparticle Green Synthesis Using Black Cumin Seed Aqueous Extract: Its Characterization and in vitro Anti- Hyperglycaemic Properties</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-Hyperglycaemia</style></keyword><keyword><style  face="normal" font="default" size="100%">Black cumin</style></keyword><keyword><style  face="normal" font="default" size="100%">ZnO Nanoparticles</style></keyword><keyword><style  face="normal" font="default" size="100%">α-amylase</style></keyword><keyword><style  face="normal" font="default" size="100%">α-glucosidase</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2025</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">17</style></volume><pages><style face="normal" font="default" size="100%">434-437</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; α-Amylase and α-glucosidase are carbohydrate metabolizing enzymes that are known to be involved in postprandial hyperglycaemia in diabetic patients. &lt;strong&gt;Objective:&lt;/strong&gt; In a bid to source potent inhibitors of these enzymes, the study synthesized zinc oxide nanoparticles and evaluated the in vitro anti-hyperglycaemic activity.&lt;strong&gt; Materials and Methods:&lt;/strong&gt; The seed aqueous extract of black Cumin (BC) was used as a capping and/or reducing agent to synthesize ZnO NPs from zinc acetate precursor. The BC-ZnONPs were characterized by microscopy (FESEM and HRTEM) and spectroscopy (UV-Vis and EDX) methods. &lt;em&gt;In vitro &lt;/em&gt;anti-hyperglycaemic evaluation was based on α-amylase and α-glucosidase inhibition assays. &lt;strong&gt;Results:&lt;/strong&gt; The BC-ZnONPs showed a spherical-to-cubical shape with a 10-50 nm size range. The UV-Vis absorption peaks at 387 and 415 nm suggest the formation of biogenic ZnO NPs. The EDX spectrum revealed 68.92% and 27.49% weight compositions of Zn and O, respectively, to further substantiate ZnO nanoparticle synthesis. The BC-ZnONPs showed notable anti-hyperglycaemic properties with IC&lt;sub&gt;50&lt;/sub&gt; of 87.72±5.13 and 124.21±15.20 μg/mL against α-amylase and α-glucosidase, respectively.&lt;strong&gt; Conclusion: &lt;/strong&gt;Black Cumin seed extract was a useful biogenic material for synthesizing ZnO NPs. The BCZnONPs showed promising anti-hyperglycaemic properties based on the notable inhibitory activities against α-amylase and α-glucosidase enzymes. Future work may include evaluating the synergistic effects of black Cumin metabolites and ZnONPs, as well as determining the in vivo toxicity profile for safety considerations.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">434</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ayodeji Oluwabunmi Oriola&lt;sup&gt;1*&lt;/sup&gt;, Pallab Kar&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemical and Physical Sciences, Walter Sisulu University, Nelson Mandela Drive, P/ Bag X1, Mthatha 5117, SOUTH AFRICA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;African Medicinal Flora and Fauna Research Niche Area, Walter Sisulu University, Nelson Mandela Drive, P/Bag X1, Mthatha 5117, SOUTH AFRICA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sri Benti Etika</style></author><author><style face="normal" font="default" size="100%">Desy Kurniawati</style></author><author><style face="normal" font="default" size="100%">Melindra Mulia</style></author><author><style face="normal" font="default" size="100%">Rahni Darussalam</style></author><author><style face="normal" font="default" size="100%">Okta Suryani</style></author><author><style face="normal" font="default" size="100%">Edi Nasra</style></author><author><style face="normal" font="default" size="100%">Nada frista</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Adsorption of Metanil Yellow Using Flavonoid Extract from Longan Peel (Dimocarpus longan): Optimization of pH and Concentration</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adsorption</style></keyword><keyword><style  face="normal" font="default" size="100%">Batch</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Longan Peel</style></keyword><keyword><style  face="normal" font="default" size="100%">Metanil Yellow</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1315-1319</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Water pollution can come from industrial waste containing various toxic pollutants, one of which is dye. Hazardous dyes are stable and resistant to biodegradation due to their complex aromatic structure, so dyes need to be treated. Metanil Yellow is a dye that is harmful to aquatic life and the human body. One method that can be used is adsorption with the batch method because it has the advantage of low cost and simple processing. Flavonoid extracts have high potential to be used as biosorbents because they have hydroxyl and carbonyl groups. This study aims to determine the potential of flavonoid extracts to adsorb metanil yellow dye using optimum pH and solution concentration and to determine its absorption capacity. The results showed that the optimum pH obtained was at pH 2 and the optimum solution concentration was at 150 ppm with an absorption capacity of 9.22078 mg/g.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1315</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sri Benti Etika, Desy Kurniawati *, Melindra Mulia, Rahni Darussalam, Okta Suryani, Edi Nasra, Nada frista&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Khadijatul Fatiyah Mubarak</style></author><author><style face="normal" font="default" size="100%">Amran Razak</style></author><author><style face="normal" font="default" size="100%">Muhammad Alwy Arifin</style></author><author><style face="normal" font="default" size="100%">Balqis</style></author><author><style face="normal" font="default" size="100%">Muhammad Kardi</style></author><author><style face="normal" font="default" size="100%">Hasnawati Amqam</style></author><author><style face="normal" font="default" size="100%">Anwar Mallongi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Analysis of Implementation of the Prolanis-Diabetes Mellitus Chronic Disease Management Program in Majene Regency</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">BPJS Health and bureaucracy</style></keyword><keyword><style  face="normal" font="default" size="100%">Cronis Disease</style></keyword><keyword><style  face="normal" font="default" size="100%">Diabetes mellitus</style></keyword><keyword><style  face="normal" font="default" size="100%">Prolanis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">644-649</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;In the context of health maintenance for BPJS health participants who suffer from chronic diseases, PROLANIS is a proactive strategy and health care system that is implemented in an integrated way involving participants, health facilities, and BPJS health. In this work, a case study methodology is combined with a qualitative method. Content analysis was employed to analyze the data. Thirteen informants—four key informants and nine routine informants—were interviewed. The research on the communication between program implementers yielded positive results, the BPJS budget was allocated effectively, and the human resource numbers of the various health centers varied, but the facilities and infrastructure were more than sufficient, and the implementation skills were strong. Proceeding by current SOPs, the bureaucracy still needs improvement and regulation, and the BPJS incentives both reward and efficiently distribute money. Conclusion: Both Community Health Centers acknowledge that funding from BPJS is fairly good. Notifications and reminders of activities have been successfully implemented in the Diabetes Mellitus Chronic Disease Management Program (PROLANIS) policy, even though only those who are active and present are the same. Infrastructure and facilities are sufficient; however, there is room for improvement in the amount, quality, and integrity of human resources. Additionally, the appointment of bureaucracy requires attention, and it may be more effectively divided.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">644</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Khadijatul Fatiyah Mubarak&lt;sup&gt;1&lt;/sup&gt;*, Amran Razak&lt;sup&gt;2&lt;/sup&gt;, Muhammad Alwy Arifin&lt;sup&gt;3&lt;/sup&gt;, Balqis&lt;sup&gt;4&lt;/sup&gt;, Muhammad Kardi&lt;sup&gt;4&lt;/sup&gt;, Hasnawati Amqam&lt;sup&gt;4&lt;/sup&gt;, Anwar Mallongi&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Postgraduate Student Department of Health Administration and Policy, Faculty of Public Health Hasanuddin University, Makassar, South Sulawesi, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Health Administration and Policy, Faculty of Public Health Hasanuddin University, Makassar, South Sulawesi, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Chairman of Health Administration and Policy, Faculty of Public Health Hasanuddin University, Makassar, South Sulawesi, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Head of the Study Program Bachelor of Public Health Faculty of Public Health Hasanuddin University Maka&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Febri Kurniawati</style></author><author><style face="normal" font="default" size="100%">Sony Wibisono Mudjanarko</style></author><author><style face="normal" font="default" size="100%">Soebagijo Adi Soelistijo</style></author><author><style face="normal" font="default" size="100%">Titong Sugihartono</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Association of Triglyceride and Glucose Index with Non-Alcoholic Fatty Liver Disease in Type 2 Diabetes Mellitus Patients</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hepatic steatosis</style></keyword><keyword><style  face="normal" font="default" size="100%">Insulin resistance</style></keyword><keyword><style  face="normal" font="default" size="100%">NAFLD</style></keyword><keyword><style  face="normal" font="default" size="100%">TyG index</style></keyword><keyword><style  face="normal" font="default" size="100%">Type 2 diabetes mellitus</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1077- 1080</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Non-alcoholic fatty liver disease (NAFLD) is significantly linked to obesity, insulin resistance (IR), metabolic syndrome, and type 2 diabetes (T2DM). There isn't a single biomarker used to diagnose NAFLD. &lt;strong&gt;Objectives:&lt;/strong&gt; Analyzing the association between triglyceride and glucose index (TyG) with NAFLD in T2DM. &lt;strong&gt;Methods: &lt;/strong&gt;This cross-sectional study aimed to assess the efficacy of TyG as a potential NAFLD biomarker. The study was conducted on 103 diabetes outpatient clinics at the Dr. Soetomo General Academic Hospital from August to October 2023. Sixty-seven subjects experienced steatosis, while those who did not experience steatosis were 36. The statistical analysis used in this study is binary logistic regression with p &amp;lt;0.05. &lt;strong&gt;Results:&lt;/strong&gt; The receiver operating characteristic curves (ROC) analysis showed a TyG cut-off value of 9.334 (AUC = 0.660). Analysis of the risk of TyG on the incidence of steatosis was carried out using binary logistic regression. The results showed that TyG was a significant risk factor for steatosis. Patients with a TyG value above 9.334 risk developing steatosis 3.567 times greater than patients with a TyG value below 9.334 (OR 95% = 1.373 – 9.270, p = 0.009). &lt;strong&gt;Conclusion: &lt;/strong&gt;A significant association between TyG and NAFLD in T2DM patients, which the TyG index may be a more effective, valuable, and uncomplicated measure for detecting and controlling NAFLD.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1077</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Febri Kurniawati&lt;sup&gt;1,2&lt;/sup&gt;, Sony Wibisono Mudjanarko&lt;sup&gt;3,4*&lt;/sup&gt;, Soebagijo Adi Soelistijo&lt;sup&gt;3,4&lt;/sup&gt;, Titong Sugihartono&lt;sup&gt;3,5&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Internal Medicine Subspecialty Study Program, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Internal Medicine, Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Internal Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Division of Endocrinology, Diabetes, and Metabolism, Department of Internal Medicine, Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Division of Gastroentero-Hepatology, Department of Internal Medicine, Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">On-Anong Somsap</style></author><author><style face="normal" font="default" size="100%">Anussara Kamnate</style></author><author><style face="normal" font="default" size="100%">Amornrat Angajchariya</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Boletus griseipurpureus Corner: Antibacterial, Antioxidant Properties and Phytochemical Compositions</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant property</style></keyword><keyword><style  face="normal" font="default" size="100%">Boletus griseipurpureus Corner</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoid compound</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolic compound</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical compositions</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">296-301</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This study aims to investigate the properties of B. griseipurpureus Corner concerning its efficacy against various bacterial strains and its antioxidant capacity, along with its phytochemical composition. The antibacterial activity was evaluated using the agar well diffusion method, revealing pronounced efficacy against gram-negative bacteria, particularly noteworthy against E. coli ESBL182, known for its antibiotic resistance. The Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) of B. griseipurpureus Corner extract against E. coli ESBL182 were determined to be 75 and 300 mg/ml, respectively. The extract exhibited bacteriostatic activity by inhibiting cell growth, leading to a reduction in optical density at 600 nm. Additionally, examination of the supernatant from untreated and treated E. coli ESBL182 cells with B. griseipurpureus Corner extract indicated absorbance values of 0.088 and 0.248 at 260 nm, and 0.045 and 0.286 at 280 nm, respectively. Further investigation utilizing a scanning electron microscope revealed alterations in the morphology of treated cells, which displayed elongation and fragmentation, in contrast to untreated cells. The DPPH assay indicated that the IC50 of B. griseipurpureus Corner extract was 31.22 mg/ml. The IC50 value obtained from the ABTS assay was 47.31 mg/ml. Additionally, the FRAP assay revealed that the concentration of ascorbic acid equivalent in B. griseipurpureus Corner extract was 1.06 mg/g crude extract. Phytochemical analysis, conducted using a spectrophotometer at wavelengths of 750 nm and 510 nm, respectively, indicated phenolic and flavonoid contents of 0.22 mg gallic acid/g fresh weight and 3.23 mg quercetin/g fresh weight in the extract.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">296</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;On-Anong Somsap&lt;sup&gt;1*&lt;/sup&gt;, Anussara Kamnate&lt;sup&gt;2&lt;/sup&gt;, Amornrat Angajchariya&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biochemistry, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Anatomy, Faculty of Medicine, Princess of Naradhiwas University, Narathiwat 96000, THAILAND.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Science and Fisheries Technology, Rajamangala University of Technology Srivijaya, Trang campus 179 Moo 3 Maifad Sikao Trang 92150, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mahresya Kamajaya</style></author><author><style face="normal" font="default" size="100%">Lita Diah Rahmawati</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Case of Spondyloarthritis with Deep Vein Thrombosis</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Complication</style></keyword><keyword><style  face="normal" font="default" size="100%">Spondyloarthritis; Deep vein thrombosis</style></keyword><keyword><style  face="normal" font="default" size="100%">Treatment</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">993-997</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Spondyloarthritis (SpA) is an autoimmune disease that has several clinical manifestations with certain characteristics. In this report, we present the case of an immobilized 54-year-old female with SpA who complained of a painful swollen left leg. Laboratory workup and imaging study supported the diagnosis of SpA complicated with deep vein thrombosis (DVT). The patient was given glucocorticoid, an anticoagulant, and medical rehabilitation. Symptoms improved following treatment. SpA increases the inflammatory state, leading to the increased risk of DVT. Holistic and comprehensive treatment is required in SpA patients with DVT to prevent further exacerbation or poorer prognosis.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Case Report</style></work-type><section><style face="normal" font="default" size="100%">993</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Mahresya Kamajaya&lt;sup&gt;1,2&lt;/sup&gt;, Lita Diah Rahmawati&lt;sup&gt;1,2,3*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Internal Medicine, Dr Soetomo General Academic Hospital, Surabaya, Indonesia.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Internal Medicine, Faculty of Medicine – UNIVERSITAS AIRLANGGA, Surabaya, Indonesia.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Division of Rheumatology, Department of Internal Medicine, Dr Soetomo General Academic Hospital, Surabaya, Indonesia.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tabisa Diniso</style></author><author><style face="normal" font="default" size="100%">Ayodeji O. Oriola</style></author><author><style face="normal" font="default" size="100%">Gugulethu M. Miya</style></author><author><style face="normal" font="default" size="100%">Simon K. Kuria</style></author><author><style face="normal" font="default" size="100%">Yiseyon S. Hosu</style></author><author><style face="normal" font="default" size="100%">Opeoluwa O. Oyedeji</style></author><author><style face="normal" font="default" size="100%">Mike O. Ojemaye</style></author><author><style face="normal" font="default" size="100%">Ludwe Majiza</style></author><author><style face="normal" font="default" size="100%">Jerry O. Adeyemi</style></author><author><style face="normal" font="default" size="100%">Adebola O. Oyedeji</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Citrus Extract-Mediated Zinc Oxide Nanoparticles and Their Capacity to Attenuate Free Radicals and Inflammation</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory capacity</style></keyword><keyword><style  face="normal" font="default" size="100%">Citrus plants</style></keyword><keyword><style  face="normal" font="default" size="100%">Free Radical Scavenging Activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Nova mandarin</style></keyword><keyword><style  face="normal" font="default" size="100%">Zinc oxide nanoparticle green synthesis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1222-1233</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The exploitation of plant materials for the green synthesis of nanoparticles (NPs) for biological applications, is considered an eco-friendly technology because it does not involve the use of toxic chemicals. &lt;strong&gt;Objective: &lt;/strong&gt;The study was carried out to synthesize citrus extract-mediated ZnO NPs and evaluate their free radical scavenging and anti-inflammatory capacity. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;ZnO NPs were green synthesized, using the peel and leaf aqueous extracts of three citrus plants: Nova mandarin, Satsuma mandarin and Eureka lemon. The citrus extract based ZnO NPs were characterized by UV-Vis and FTIR spectroscopy, microscopy (SEM and TEM), EDX and XRD analyses. They were screened against 2,2-diphenyl-1-picrylhydrazyl (DPPH) and nitric oxide (NO) free radicals. Finally, their inhibitory effects against egg albumin denaturation (EAD) were determined spectrophotometrically. &lt;strong&gt;Results:&lt;/strong&gt; The six afforded biogenic NPs consistently exhibited FTIR vibrational band around 500 cm-1, which is characteristics of a metal oxide (Zn-O) band. They also showed UV-Vis absorption peaks at 387 and 415 nm, suggesting the formation of ZnO NPs. Nova mandarin peel (NMP) ZnO NPs exhibited the best DPPH and NO radical scavenging activities, with 50% inhibitory concentration (IC50) of 7.61±0.69 and 19.93±0.40 μg/mL, respectively. It also gave the best inhibition against EAD, with an IC50 of 14.80±1.29 μg/mL. Morphological assessment of NMP extract-based ZnO NPs revealed rod-shaped particles at 35-50 nm range. &lt;strong&gt;Conclusion: &lt;/strong&gt;It has been shown through this study that citrus extract based ZnO NPs, especially those prepared with NMP, may have the capacity to attenuate free radical release and inflammation in biological systems.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1222</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Tabisa Diniso&lt;sup&gt;1&lt;/sup&gt;, Ayodeji O. Oriola&lt;sup&gt;1*&lt;/sup&gt;, Gugulethu M. Miya&lt;sup&gt;1&lt;/sup&gt;, Simon K. Kuria&lt;sup&gt;2&lt;/sup&gt;, Yiseyon S. Hosu&lt;sup&gt;3&lt;/sup&gt;, Opeoluwa O. Oyedeji&lt;sup&gt;4&lt;/sup&gt;, Mike O. Ojemaye&lt;sup&gt;4&lt;/sup&gt;, Ludwe Majiza&lt;sup&gt;5&lt;/sup&gt;, Jerry O. Adeyemi&lt;sup&gt;1&lt;/sup&gt;, Adebola O. Oyedeji&lt;sup&gt;1*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemical and Physical Sciences, Walter Sisulu University, Mthatha, 5117, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biological and Environmental Sciences, Walter Sisulu University, Mthatha, 5117, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Business Management and Economics, Faculty of Economics and Financial Sciences.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Chemistry, University of Fort Hare, Alice, 5700, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Vunikhaya (PTY)LTD, Burnshill Location, Keiskammahoek, 5670, SOUTH AFRICA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Harris Kristanto Gunawan</style></author><author><style face="normal" font="default" size="100%">Evelyn Komaratih</style></author><author><style face="normal" font="default" size="100%">Rozalina Loebis</style></author><author><style face="normal" font="default" size="100%">Djoko Agus Purwanto</style></author><author><style face="normal" font="default" size="100%">Luki Indriaswati</style></author><author><style face="normal" font="default" size="100%">Wimbo Sasono</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparison of Asiatic Acid and Dexamethasone Effect on Interleukin-4 Expression and Eosinophile Cell Count Following Strabismus Surgery: An Experimental Study in New Zealand Rabbit</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Asiatic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Dexamethasone</style></keyword><keyword><style  face="normal" font="default" size="100%">Eosinophil</style></keyword><keyword><style  face="normal" font="default" size="100%">Interleukin-4</style></keyword><keyword><style  face="normal" font="default" size="100%">Strabismus</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1411-1417</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Postoperative strabismus inflammation can lead to fibrotic tissue formation. Dexamethasone, while generally effective as an anti-inflammatory post-surgery medication, can increase IOP and blood sugar levels. Research on asiatic acid suggests its potential as an anti-inflammatory and anti-fibrotic agent. &lt;strong&gt;Methods:&lt;/strong&gt; Superior rectus recession was conducted on 20 rabbits, which were divided into five groups based on the subconjunctival injection substance: aquadest, dexamethasone, asiatic acid at a concentration of 0.4 mg/0.5 mL, 0.8 mg/0.5 mL, and 1.6 mg/0.5 mL. After three days, exenteration was performed, and an immunohistochemical examination was performed to assess interleukin-4 expression. Hematoxylin and eosin staining was performed to assess eosinophile cell count. SPSS 26.0 facilitated the data analysis using the Kruskal-Wallis and Wilcoxon Mann-Whitney tests. P&amp;lt;0.05 was considered significant statistically. &lt;strong&gt;Results:&lt;/strong&gt; This study showed that interleukin-4 expression in the asiatic acid 0.4 mg/0.5 mL group was significantly decreased compared to the aquadest group (P = 0.029) and dexamethasone group (P = 0.029). Higher-dose groups did not exhibit a significant decrease. Dexamethasone also did not exhibit a significant decrease compare to aquadest. There was no significant reduction of eosinophile cell count among all groups.&lt;strong&gt; Conclusions:&lt;/strong&gt; This study highlighted the potential of asiatic acid, particularly at the concentration of 0.4 mg/0.5 mL, in reducing the inflammatory response, specifically interleukin-4 expression, after strabismus surgery in New Zealand rabbits.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1411</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Harris Kristanto Gunawan&lt;sup&gt;1&lt;/sup&gt;, Evelyn Komaratih&lt;sup&gt;1*&lt;/sup&gt;, Rozalina Loebis&lt;sup&gt;1&lt;/sup&gt;, Djoko Agus Purwanto&lt;sup&gt;2&lt;/sup&gt;, Luki Indriaswati&lt;sup&gt;1&lt;/sup&gt;, Wimbo Sasono&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Ophthalmology, Dr. Soetomo General Academic Hospital, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dewi Rochmawati</style></author><author><style face="normal" font="default" size="100%">Puspa Wardhani</style></author><author><style face="normal" font="default" size="100%">Yessy Puspitasari</style></author><author><style face="normal" font="default" size="100%">Tutik Kusmiati</style></author><author><style face="normal" font="default" size="100%">Atika</style></author><author><style face="normal" font="default" size="100%">Hartono Kahar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Concordance of Sputum and Feces Samples for Detecting Mycobacterium Tuberculosis using Xpert® MTB/RIF Ultra</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Feces AFB test</style></keyword><keyword><style  face="normal" font="default" size="100%">Feces Xpert® MTB/RIF Ultra test</style></keyword><keyword><style  face="normal" font="default" size="100%">Mycobacterium tuberculosis (MTB)</style></keyword><keyword><style  face="normal" font="default" size="100%">rifampicin resistance test</style></keyword><keyword><style  face="normal" font="default" size="100%">Xpert® MTB/RIF Ultra</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">167-173</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Tuberculosis (TB) remains a disease with high morbidity and mortality worldwide, and Indonesia ranks among the countries with the highest TB prevalence. There is a need to develop improved detection tools and explore alternative sample sources beyond sputum. Feces samples are one such nonsputum alternative. Xpert® MTB/RIF Ultra is a novel diagnostic tool used in Indonesia. This study aims to assess the concordance of both sputum and feces samples in detecting Mycobacterium tuberculosis (MTB) using Xpert® MTB/RIF Ultra. &lt;strong&gt;Methods: &lt;/strong&gt;An analytical observational study with a cross-sectional design was conducted on TB subjects at Dr. Soetomo Regional Public Hospital (RSUD Dr. Soetomo), Surabaya, and several community health centers (puskesmas) in Surabaya. Sputum and feces samples were collected from the same subjects. These subjects underwent Feces acid-fast bacilli (AFB) tests, sputum and Feces Xpert® MTB/RIF Ultra tests, and sputum culture tests (considered the gold standard), as well as rifampicin resistance tests for positive cultures. Sensitivity and positive predictive value (PPV) tests were conducted using Medcalc software, and the concordance test employed the Kappa value. &lt;strong&gt;Results:&lt;/strong&gt; The study involved 71 research subjects. The sensitivity of Feces AFB tests, sputum, and Feces Xpert® MTB/RIF Ultra tests was 7.3%, 97.6%, and 97.6%, respectively. The Cohen's Kappa consistency test for Feces AFB tests and sputum culture produced a Kappa value of 0.063 (p &amp;gt; 0.05). The Cohen's Kappa consistency test on sputum and Feces Xpert® MTB/RIF Ultra tests yielded a Kappa value of 0.409 (p &amp;lt; 0.05). The Cohen's Kappa consistency test on sputum and Feces Xpert® MTB/RIF Ultra tests compared with the rifampicin resistance tests resulted in Kappa values of 0.902 and 0.951 (p &amp;lt; 0.05). The CT value of Feces Xpert® MTB/RIF Ultra tests was higher than that of sputum Xpert® MTB/RIF Ultra tests. &lt;strong&gt;Conclusion:&lt;/strong&gt; A concordance exists between the results of sputum and Feces Xpert® MTB/RIF Ultra tests, but no concordance is observed between the results of Feces AFB tests and sputum culture tests. The higher CT value of Feces Xpert® MTB/RIF Ultra tests compared to sputum Xpert® MTB/RIF Ultra tests indicates a lower bacterial load in feces. Feces can be considered a viable alternative sample to sputum for MTB detection using Xpert® MTB/RIF Ultra.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">167</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Dewi Rochmawati&lt;sup&gt;1&lt;/sup&gt;, Puspa Wardhani&lt;sup&gt;1,2,3&lt;/sup&gt;, Yessy Puspitasari&lt;sup&gt;1&lt;/sup&gt;, Tutik Kusmiati&lt;sup&gt;4&lt;/sup&gt;, Atika&lt;sup&gt;5&lt;/sup&gt;, Hartono Kahar&lt;sup&gt;1,3&lt;/sup&gt;,*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Clinical Pathology, Faculty of Medicine, Universitas Airlangga, Dr. Soetomo General Academic Hospital, Surabaya, East Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Institute of Tropical Diseases, Universitas Airlangga, Surabaya, East Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Postgraduate School of Universitas Airlangga, Surabaya, East Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pulmonology and Respiratory Medicine, Faculty of Medicine, Universitas Airlangga, Dr. Soetomo General Academic Hospital, Surabaya, East Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Public Health Sciences Preventive Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, East Java, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Etty Hary Kusumastuti</style></author><author><style face="normal" font="default" size="100%">Stephanie Natasha Djuanda</style></author><author><style face="normal" font="default" size="100%">Grace Ariani</style></author><author><style face="normal" font="default" size="100%">Gondo Mastutik</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Correlation of N-Cadherin and MMP-9 Expression with Regional Nodal Metastasis in Laryngeal Squamous Cell Carcinoma</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Laryngeal cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Metastasis</style></keyword><keyword><style  face="normal" font="default" size="100%">MMP-9</style></keyword><keyword><style  face="normal" font="default" size="100%">N stages</style></keyword><keyword><style  face="normal" font="default" size="100%">N-cadherin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">679-683</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; In laryngeal carcinoma, regional nodal metastasis serves as a significant prognostic factor. A special biomarker is needed to predict the status of nodal metastases. N-cadherin, a binding protein, aids in cell migration and enabling tumor cells to spread to new locations. The involvement of matrix metalloproteinase-9 (MMP-9) in metastasis includes fostering the dissemination of tumor cells from the primary tumor and enhancing tumor cell motility. &lt;strong&gt;Objective:&lt;/strong&gt; This study seeks to explore the distinctions and relationships in N-cadherin and MMP-9 expression among patients with laryngeal squamous cell carcinoma at various N stages. &lt;strong&gt;Methods:&lt;/strong&gt; Employing a cross-sectional approach, this study conducted an analytic observational investigation on formalin-fixed paraffin-embedded patients whose histopathological diagnosis is laryngeal squamous cell carcinoma in the Pathology Laboratory of Dr. Soetomo Regional Public Hospital in 2018–2021. The samples were divided into N stages based on radiological imaging from the CT scan. Immunohistochemistry examinations were performed using N-cadherin and MMP-9 antibodies and scored using the immunoreactive score (IRS), based on percentage and intensity. The differences in expression and correlation between N-cadherin and MMP-9 were analyzed using statistical tests. &lt;strong&gt;Results:&lt;/strong&gt; Statistical insignificance was observed in N-cadherin expression at various N stages (p = 0.099). There were significant differences in MMP-9 expressions at various N stages (p = 0.0006338). There was no correlation between N-cadherin and MMP-9 expression at various N stages in laryngeal squamous cell carcinoma (p = 0.0638, rs = 0.27). &lt;strong&gt;Conclusion:&lt;/strong&gt; In laryngeal squamous cell carcinoma, MMP-9 serves as a predictor for lymph node metastasis, which, if present, deteriorates the patient's prognosis.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">679</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Etty Hary Kusumastuti&lt;sup&gt;1,2&lt;/sup&gt;*, Stephanie Natasha Djuanda&lt;sup&gt;1,2&lt;/sup&gt;, Grace Ariani&lt;sup&gt;1,2&lt;/sup&gt;, Gondo Mastutik&lt;sup&gt;2&lt;/sup&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Dr Soetomo Academic General Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Anatomical Pathology, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Novi Fajar Utami</style></author><author><style face="normal" font="default" size="100%">Berna Elya</style></author><author><style face="normal" font="default" size="100%">Hayun Hayun</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Syamsu Nur</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Bacterial Enzymes on Reducing Chlorogenic Acid Levels in Cascara Robusta Coffee (Coffea canephora L.)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Bacillus subtilis</style></keyword><keyword><style  face="normal" font="default" size="100%">Cascara</style></keyword><keyword><style  face="normal" font="default" size="100%">Chlorogenic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">332-335</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Coffee skin by-products, namely cascara, have several benefits, namely can ward off free radicals, with the ability of cascara to ward off free radicals so that cascara can potentially prevent the emergence of cancer cells. Cascara contains active compounds caffeine 1.3%, chlorogenic acid 2.6%, and caffeic acid 1.6%. &lt;strong&gt;Objective:&lt;/strong&gt; This study aims to determine chlorogenic acid levels in decaffeinated robusta coffee (Coffea canephora L.) and see the influence of Bacillus subtilis bacteria on reducing chlorogenic acid levels. &lt;strong&gt;Methods:&lt;/strong&gt; The experiment was conducted from June to August 2022 in the Pharmacy Laboratory, Faculty of Mathematics and Natural Sciences, Universitas Pakuan, Indonesia. Cascara robusta coffee is fermented using Bacillus subtilis with a concentration of 6% and a time of 24 hours. After fermentation, the extraction is carried out using the UAE (Ultrasonic Assisted Extraction) method. The chlorogenic acid levels and zero control of cascara robusta coffee obtained were then analyzed using Statistical Package for the Social Science (SPSS) with the Paired sample t-test method previously carried out with normality test and homogeneity test first. &lt;strong&gt;Results:&lt;/strong&gt; The study found chlorogenic acid levels produced from cascara robusta coffee that had undergone decaffeination. Quantitative analysis of chlorogenic acid levels in cascara robusta coffee was carried out using HPLC mobile phase methanolwater (adjust Orthoposphat pH 2.4), flow rate 0.7 mL/minute, with an isocratic system of an average of 14.8597%. &lt;strong&gt;Conclusion:&lt;/strong&gt; Chlorogenic acid levels in robusta coffee cascara decaffeinated by microbial enzymes can affect chlorogenic acid levels.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">332</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Novi Fajar Utami&lt;sup&gt;1,2&lt;/sup&gt;, Berna Elya&lt;sup&gt;1*&lt;/sup&gt;, Hayun Hayun&lt;sup&gt;3&lt;/sup&gt;, Kusmardi Kusmardi&lt;sup&gt;4,5,6&lt;/sup&gt;, Syamsu Nur&lt;sup&gt;7&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Phytochemistry and Pharmacognosy, Faculty of Pharmacy, Universitas Indonesia, Depok 16424 West Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Math and Science, Universitas Pakuan, Jl. Raya Pakuan 1 Bogor, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Pharmacy, Universitas Indonesia, Depok 16424 West Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Anatomic Pathology, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya No.6, Jakarta, 10430, Jakarta, Indonesia, 10430 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Drug Development Research Cluster, Indonesia Medical Educational and Research Institute, Jl. Salemba Raya No.6, Jakarta 10340, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Human Cancer Research Cluster, Indonesia Medical Educational and Research Institute, Jl. Salemba Raya No.6, Jakarta 10340, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Pharmaceutical Chemistry, Almarisah Madani University, Makassar, South Sulawesi, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Manggiasih Dwiayu Larasati</style></author><author><style face="normal" font="default" size="100%">Silvia W. Lestari</style></author><author><style face="normal" font="default" size="100%">Mulyoto Pangestu</style></author><author><style face="normal" font="default" size="100%">Andon Hestiantoro</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Cryopreservation on the Sperm Ultrastructure of Mus Musculus Albinus Strain DDY: Comparison of Nakagata vs Modified vs Kitazato Cryoprotectants</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">cryopreservation</style></keyword><keyword><style  face="normal" font="default" size="100%">glycerol</style></keyword><keyword><style  face="normal" font="default" size="100%">mice sperm</style></keyword><keyword><style  face="normal" font="default" size="100%">raffinose</style></keyword><keyword><style  face="normal" font="default" size="100%">Scanning electron microscope</style></keyword><keyword><style  face="normal" font="default" size="100%">Trehalose</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">563-569</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Sperm morphology analysis is very necessary to understand male fertility and the etiology of infertility. Currently, scanning electron microscopy (SEM) has been widely used to determine surface topology. In this study, we will compare the effects of spermatozoa cryopreservation using three different types of cryoprotectants, namely Nakagata, modification and Kitazato. The cryoprotectant compositions used are Nakagata (raffinose and skim milk), modified (glycerol and raffinose) and Kitazato (glycerol and trehalose). &lt;strong&gt;Methods:&lt;/strong&gt; SEM analysis was carried out on 8 sperm samples before cryopreservation and after the freeze-thaw process. &lt;strong&gt;Results:&lt;/strong&gt; The results obtain showed that cryoprotectant modification was able to protect spermatozoa morphology better than Nakagata and Kitazato. Analysis revealed damage to plasma membrane, acrosome and loss of mitochondria in all treatment groups compared to fresh sperm. SEM showed obvious signs of post-thaw damage such as missing plasma membranes, sperm showing damaged acrosomes and mitochondria in the middle showing structural disorganization. &lt;strong&gt;Conclusion: &lt;/strong&gt;SEM revealed that cryopreservation caused ultrastructural damage to mice sperm due to freezing and thawing. These details provide valuable data for further research to minimize the damage caused by cryopreservation to mice sperm. Apart from that, further examination using TEM is recommended to obtain a more comprehensive picture.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">563</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Manggiasih Dwiayu Larasati&lt;sup&gt;1&lt;/sup&gt;, Silvia W. Lestari&lt;sup&gt;2&lt;/sup&gt;,* Mulyoto Pangestu&lt;sup&gt;3&lt;/sup&gt;, Andon Hestiantoro&lt;sup&gt;4&lt;/sup&gt;, Kusmardi Kusmardi&lt;sup&gt;5-7&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctoral Program in Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya No. 6, Jakarta 10430 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jakarta 10430 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Education Program in Reproduction and Development, Department of Obstetrics and Gynecology, School of Clinical Sciences, Monash University, Victoria, AUSTRALIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, Faculty of Medicine, Universitas Indonesia, Jakarta 10430 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Pathological Anatomy, Faculty of Medicine, Universitas Indonesia, Jalan Salemba Raya No. 6, Jakarta 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Drug Development Research Center, Indonesia Medical Education and Research Institute (IMERI), Universitas Indonesia, Jalan Salemba Raya No. 6, Jakarta 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Human Cancer Research Center, Indonesia Medical Education and Research Institute (IMERI), Universitas Indonesia, Jalan Salemba Raya No. 6, Jakarta 10430, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sheinni Paradise</style></author><author><style face="normal" font="default" size="100%">M. Alimin Maidin</style></author><author><style face="normal" font="default" size="100%">Amran Razak</style></author><author><style face="normal" font="default" size="100%">Abdul Rahman KadirHegazy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Diet, Medication, Physical Activity on Glycemic Control of Type-2 Diabetes Mellitus Patients in Makassar City</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1110-1113</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The prevalence of diabetes mellitus continues to increase every year with various complications. This is caused by an unhealthy lifestyle. The complex management of type 2 diabetes mellitus triggers problems that cause therapeutic goals not to be achieved. The risk of complications is higher due to lack of attention to lifestyle including diet. A good diet, medication and physical activity are considered capable of improving blood sugar control so that the quality of life of people with diabetes mellitus becomes better. Objective: to analyze the effect of diet, medication, physical activity on glycemic control of patients with type 2 diabetes mellitus. Methods: the study was conducted in December 2023-February 2024 at Kassi-Kassi Health Center and Kalukubodoa Health Center, Makassar City, South Sulawesi. The sample size was type 2 diabetes mellitus patients in Kassi-Kassi Health Center as many as 184 people and Kalukubodoa Health Center as many as 168 people. The research group consisted of 2 groups, namely at Puskesmas Kassi- Kassi and Puskesmas Kalukubodoa with a combination intervention of food menu modules for diabetic patients and leaflets and Puskesmas Kassi-Kassi with food menu modules for diabetic patients. Both research groups were intervened for 3 (three) months with the assistance of doctors and nutritionists. There are two stages in this study, namely stage 1 making a prolanis intervention model with quantitative methods followed by stage 2, namely the intervention of food menu modules for diabetic patients and with quasi-experimental methods with a non-randomized pretest postest design. Results: In the aspects of diet, medication, physical activity there is a significant increase in Kassi-Kassi Health Center and Kalukubodoa Health Center (p=0.00) on glycemic control of type-2 diabetes mellitus patients. Conclusion: The results of the trial of the food menu module for patients with type 2 diabetes mellitus showed a value of 80%, meaning that the module was feasible to use based on the assessment of the material expert. Diet, medication, physical activity have a statistical effect and there is a difference in the mean value of glycemic control of type-2 diabetes mellitus patients.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1110</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sheinni Paradise*, M. Alimin Maidin, Amran Razak, Abdul Rahman Kadir&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Hasanuddin University, Makassar City, Province South Sulawesi, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zuraida</style></author><author><style face="normal" font="default" size="100%">Silvia Werdhy Lestari</style></author><author><style face="normal" font="default" size="100%">Mulyoto Pangestu</style></author><author><style face="normal" font="default" size="100%">Andon Hestiantoro</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Glutathione Supplementation in Cryoprotectant Modification on Tyrosine Phosphorylation, Acrosin Expression and Acrosome Reaction of Post-Thawing Spermatozoa Quality</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">acrosin expression</style></keyword><keyword><style  face="normal" font="default" size="100%">acrosome reaction</style></keyword><keyword><style  face="normal" font="default" size="100%">CPA modification</style></keyword><keyword><style  face="normal" font="default" size="100%">glutathione (GSH)</style></keyword><keyword><style  face="normal" font="default" size="100%">spermatozoa cryopreservation</style></keyword><keyword><style  face="normal" font="default" size="100%">tyrosine phosphorylation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">554-562</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Tyrosine phosphorylation, acrosin, and acrosome reaction play an important role in fertilisation. However, cryopreservation causes changes in tyrosine phosphorylation, acrosin expression, and acrosome reaction which affect the quality of spermatozoa. Cryoprotectant media added with antioxidants is needed to protect Spermatozoa from the effects of cryopreservation so that the quality of spermatozoa can be maintained. &lt;strong&gt;Objectives:&lt;/strong&gt; This research examined the effect of glutathione (GSH) supplementation in cryopreservation media on tyrosine phosphorylation, acrosin expression, and acrosome reaction. In this research, pure modified Cryoprotectant (CPA) was compared with CPA supplemented with GSH in three different concentrations. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The research sample was male mus musculus albinus strain Deutchland Denken Yoken (DDY). Mice spermatozoa was cryopreserved and several parameters were measured including tyrosine phosphorylation, acrosin expression, and acrosome reaction. &lt;strong&gt;Results:&lt;/strong&gt; The addition of GSH to the modified CPA increased tyrosine phosphorylation, acrosin expression, and acrosome reaction (maintaining acrosome integrity). The group with 1.00 mM GSH obtained the highest results among the other groups. Significant increases were found in tyrosine phosphorylation, acrosin expression, and acrosome reaction after the addition of 1.00 mM GSH. &lt;strong&gt;Conclusion:&lt;/strong&gt; Glutathione supplementation in modified CPA can increase tyrosine phosphorylation, acrosin expression, and acrosome reaction of frozen-thawed spermatozoa. Treatment using GSH at a dose of 1.00 mM is the most effective and modification of CPA with the addition of glutathione can improve the tyrosine phosphorylation, acrosin expression and acrosome reaction in cryopreserved spermatozoa.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">554</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Zuraida&lt;sup&gt;1,2&lt;/sup&gt;, Silvia Werdhy Lestari&lt;sup&gt;3&lt;/sup&gt;,*, Mulyoto Pangestu&lt;sup&gt;4&lt;/sup&gt;, Andon Hestiantoro&lt;sup&gt;5&lt;/sup&gt;, Kusmardi Kusmardi&lt;sup&gt;6-8&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctoral Program in Biomedical Sciences, Faculty of Medicine, Universitas Indonesia; Jl. Salemba Raya No. 6, Jakarta 10430 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Midwifery, Faculty of Health, Universitas Fort de Kock Bukittinggi, Jl. Soekarno Hatta No. 11, Bukittinggi, Sumbar 26117 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jakarta 10430 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Education Program in Reproduction and Development, Department of Obstetrics and Gynecology, School of Clinical Sciences, Monash University, Victoria, AUSTRALIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, Faculty of Medicine, Universitas Indonesia, Jakarta 10430 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Pathological Anatomy, Faculty of Medicine, Universitas Indonesia, Jalan Salemba Raya No. 6, Jakarta 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Drug Development Research Center, Indonesia Medical Education and Research Institute (IMERI), Universitas Indonesia, Jalan Salemba Raya No. 6, Jakarta 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Human Cancer Research Center, Indonesia Medical Education and Research Institute (IMERI), Universitas Indonesia, Jalan Salemba Raya No. 6, Jakarta 10430, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Andika Perdani Somawi</style></author><author><style face="normal" font="default" size="100%">Nancy Margarita Rehatta</style></author><author><style face="normal" font="default" size="100%">Prihatma Kriswidyatomo</style></author><author><style face="normal" font="default" size="100%">Kohar Hari Santoso</style></author><author><style face="normal" font="default" size="100%">Hamzah</style></author><author><style face="normal" font="default" size="100%">Pudji Lestari</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Propofol TIVA Compared Sevoflurane Inhalation Anesthesia on Triglyceride Levels After Elective Craniotomy Surgery</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Craniotomy</style></keyword><keyword><style  face="normal" font="default" size="100%">Sevoflurane</style></keyword><keyword><style  face="normal" font="default" size="100%">TIVA propofol</style></keyword><keyword><style  face="normal" font="default" size="100%">Triglycerides</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">597-601</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Propofol TIVA has been shown to be more effective than sevoflurane in craniotomy surgery. Propofol TIVA offers the benefit of giving better brain relaxation during surgery while also being less expensive than sevoflurane. Nonetheless, it is important to highlight that propofol has side effects that should be considered. Large doses and prolonged anesthesia may result in increased triglycerides (lipids) as well as Propofol Infusion Syndrome (PRIS). As part of their investigation into the detrimental effects of propofol, researchers discovered the necessity for controls to avoid confusing the effects of the surgery itself. Therefore, sevoflurane was chosen as the control group to comprehend and analyze the effects of propofol more accurately. &lt;strong&gt;Methods: &lt;/strong&gt;A prospective observational study analysis was conducted on elective craniotomy patients at RSUD Dr. Soetomo from November to December 2023. 52 subjects were divided into two groups, namely the TIVA Propofol and Sevoflurane Inhalation groups. Each group will be examined for preoperative triglyceride levels and postoperative triglyceride levels while already in the ICU. &lt;strong&gt;Results:&lt;/strong&gt; Postoperative triglyceride levels in the Propofol TIVA group were significantly higher. In the comparison test between the two anesthesia methods on triglyceride levels, there was a significant effect in the Propofol TIVA group. In the test of the relationship between the duration of anesthesia in both groups, there was no significant relationship. In the test of the relationship between the total dose of propofol and triglyceride levels, it was found that the greater the dose of propofol used, the higher the increase in triglyceride levels. In the test of the relationship between the total amount of sevoflurane and triglyceride levels, it was found that the greater the dose of sevoflurane used, the greater the decrease in triglyceride levels, which was statistically not significant.&lt;strong&gt; Conclusion:&lt;/strong&gt; TIVA Propofol increases triglyceride levels compared to sevoflurane inhalation in patients undergoing elective craniotomies.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">597</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Andika Perdani Somawi&lt;sup&gt;1&lt;/sup&gt;*, Nancy Margarita Rehatta&lt;sup&gt;1&lt;/sup&gt;, Prihatma Kriswidyatomo&lt;sup&gt;1&lt;/sup&gt;, Kohar Hari Santoso&lt;sup&gt;1&lt;/sup&gt;, Hamzah&lt;sup&gt;1&lt;/sup&gt;, Pudji Lestari&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Departement of Anesthesiology and Reanimation, Faculty of Medicine, Universitas Airlangga, Dr. Soetomo General Academic Hospital, Surabaya, East Java, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Departement of Public Health Science Preventive Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, East Java, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chutharat Saereewat</style></author><author><style face="normal" font="default" size="100%">Kusuma Sriyakul</style></author><author><style face="normal" font="default" size="100%">Parunkul Tungsukruthai</style></author><author><style face="normal" font="default" size="100%">Sunyarn Niempoog</style></author><author><style face="normal" font="default" size="100%">Sucharat Tungsukruthai</style></author><author><style face="normal" font="default" size="100%">Chuntida Kamalashiran</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efficacy and Safety of Traditional Transdermal Patch (Ya-Pok- Dud-Pid) in Primary Knee Osteoarthritis Patients: A Randomized Controlled Trial</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Diclofenac</style></keyword><keyword><style  face="normal" font="default" size="100%">Osteoarthritis of knee</style></keyword><keyword><style  face="normal" font="default" size="100%">Traditional</style></keyword><keyword><style  face="normal" font="default" size="100%">Transdermal Patch</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">570-575</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Patients with Knee Osteoarthritis (KOA) have a progressive decline in their social and physical abilities, which affects their quality of life. The Thai Traditional Transdermal Patch (Ya-Pok-Dud- Pid; YP) has been widely used for the treatment of KOA. &lt;strong&gt;Objective:&lt;/strong&gt; To determine the clinical efficacy and safety of YP in comparison with diclofenac gel (DG) for the treatment of KOA.&lt;strong&gt; Methods:&lt;/strong&gt; 74 primary KOA Patients were enrolled and randomly assigned to YP groups or DG groups. The outcomes were assessed the Visual Analog Scale (VAS), Time Up and Go (TUG), Active Knee Flexion (AKF) and Passive Knee Flexion, chair sit and reach, and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). &lt;strong&gt;Results:&lt;/strong&gt; YP and DG significantly improved VAS, TUG, AKF, PKF, chair sit and reach, and WOMAC (p &amp;lt; 0.05). Remarkably, YP experienced the same immediate pain relief after day 1 treatment as DG. The VAS scores of the YP group exhibited a significant reduction from 60±11.06 to 38.92±17.76, while DG decreased VAS score from 61.24±17.84 to 39.19±20.05 (p &amp;lt;0.001). However, there was no significant difference between the two treatment groups. For adverse event, skin reaction (rash, itchy, and dry skin) was noted in the YP group because of the participant receiving YP for an extended period. Altogether, YP has a similar effect to diclofenac gel on pain severity and physical function in patients with knee osteoarthritis. &lt;strong&gt;Conclusion:&lt;/strong&gt; YP is recommended as a natural therapeutic agent with efficacy and safety treatment for knee osteoarthritis.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">570</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Chutharat Saereewat&lt;sup&gt;1&lt;/sup&gt;, Kusuma Sriyakul1, Parunkul Tungsukruthai&lt;sup&gt;1&lt;/sup&gt;, Sunyarn Niempoog&lt;sup&gt;2&lt;/sup&gt;, Sucharat Tungsukruthai&lt;sup&gt;3&lt;/sup&gt;, Chuntida Kamalashiran&lt;sup&gt;1&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Integrative Medicine, Chulabhorn International College of Medicine, Thammasat University (Rangsit Campus), Pathum Thani, 12120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Orthopedic, Thammasat University (Rangsit Campus), Pathum Thani, 12120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Division of Health and Applied Sciences, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90110, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Neni Wahyu Hastuti</style></author><author><style face="normal" font="default" size="100%">Delfitri Munir</style></author><author><style face="normal" font="default" size="100%">Reno Keumalazia Kamarlis</style></author><author><style face="normal" font="default" size="100%">Bintang Yinke Magdalena Sinag</style></author><author><style face="normal" font="default" size="100%">Adang Bachtiar</style></author><author><style face="normal" font="default" size="100%">Farhat</style></author><author><style face="normal" font="default" size="100%">Amira Permatasari Tarigan</style></author><author><style face="normal" font="default" size="100%">Delyuzar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Eosinophil Cell and Mass Appearance in Atypical Mycobacterium Infection of Lymphadenitis</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Atypical mycobacterium</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytology</style></keyword><keyword><style  face="normal" font="default" size="100%">Eosinophil</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">664-667</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Atypical mycobacterium (ATM) is acid fast bacilli not including tuberculosis and may had opportunistic feature in environment either in air or soil. While symptoms of ATM infection may look similar with typical tuberculosis, these specific group of disease were harder to treat and would necessitate longer antibiotics consumption. While PCR may readily available to detect ATM, anatomical pathology method such as biopsy may be a cheaper alternative in low-resource settings to differentiate between atypical and typical mycobacterium infection. &lt;strong&gt;Aim:&lt;/strong&gt; To analyze correlation between eosinophil cells and eosinophil mass with ATM in lymphadenopathy patient. &lt;strong&gt;Methods: &lt;/strong&gt;This study is an analytical observational study with cross-sectional design which aimed to review diagnostic abilities of eosinophil cell and mass to detect ATM. Patient would undergo both PCR as gold standard of diagnosis and cytology biopsy aspiration as comparative diagnostic modalities. Data would be presented from SPSS v. 25. &lt;strong&gt;Results:&lt;/strong&gt; We collected 70 subjects that fulfill inclusion and exclusion criteria. Most samples were dominated by female in relatively young age. There are 37 patients with ATM in which 75,7% patients cytology result shown expression of eosinophil cells and 71,4% patients shown eosinophilic mass. Chi-square test revealed that statistical significance existed between eosinophilic cells with ATM. However, such statistical significance was not found between eosinophilic mass and ATM. &lt;strong&gt;Conclusion:&lt;/strong&gt; Eosinophilic cell can be used as alternative diagnostic modalities in diagnosing ATM. Further studies should further examine pathophysiological correlations and diagnostic power.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">664</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Neni Wahyu Hastuti&lt;sup&gt;1&lt;/sup&gt;*, Delfitri Munir&lt;sup&gt;2&lt;/sup&gt;, Reno Keumalazia Kamarlis&lt;sup&gt;3&lt;/sup&gt;, Bintang Yinke Magdalena Sinaga&lt;sup&gt;4&lt;/sup&gt;, Adang Bachtiar&lt;sup&gt;5&lt;/sup&gt;, Farhat&lt;sup&gt;2&lt;/sup&gt;, Amira Permatasari Tarigan&lt;sup&gt;4&lt;/sup&gt;, Delyuzar&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;6&lt;/strong&gt; &lt;/sup&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Philosophy Doctor in Medicine Program, Faculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Ear, Nose, Throat, Head and Neck Surgery, Faculty of Medicine, Universitas Sumatera Utara, Medan, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Anatomical Pathology, dr Zainoel Abidien Hospital, Universitas Syiah Kuala, Banda Aceh, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pulmonology and Respiratory Medicine, Faculty of Medicine, Universitas Sumatera Utara, Medan, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Health Policy and Administration, School of Public Health, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Anatomical Pathology, Faculty of Medicine, Universitas Sumatera Utara, Medan, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dewi Sartika</style></author><author><style face="normal" font="default" size="100%">Amran Razak</style></author><author><style face="normal" font="default" size="100%">Muhammad Alwy Arifin</style></author><author><style face="normal" font="default" size="100%">Balqis</style></author><author><style face="normal" font="default" size="100%">Muhammad Kardi</style></author><author><style face="normal" font="default" size="100%">Nurhaedar Jafar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of the Antenatal Care Service Program at the Tojo Una-Una District Health Office</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antenatal Care Services</style></keyword><keyword><style  face="normal" font="default" size="100%">Health Service</style></keyword><keyword><style  face="normal" font="default" size="100%">Program Evaluation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">615-623</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Through ANC, various information and education related to pregnancy and childbirth preparation can be provided to mothers as early as possible. ANC service is a program provided to pregnant women as a form of preventive service for disorders during pregnancy and also functions as an early detection of health problems experienced by pregnant women. Objective: This research is to evaluate the antenatal care service program in Tojo Una-una Regency based on Input, Process and Output. Method: This type of research uses a qualitative research design through in-depth interview techniques and document reviews. Determining informants using purposive sampling technique, numbering 11 informants. Data were collected through triangulation techniques, namely in-depth interviews, observation and documentation using interview guides. Results: research shows that the input to the antenatal care service program in terms of funding used for the ANC service program is still insufficient where the funds come from APBN funds in the form of non-physical DAK, BOK and BPJS funds, apart from that the availability of human resources is still inadequate, Some community health centers still feel inadequate because they have a large working area, making it difficult to carry out activities in the field or at the community health center because the village midwife, who is supposed to only work at the village health post, has concurrent duties at the community health center. In the process component, the community health center has implemented the antenatal care service program in accordance with the plan, although there are still several obstacles such as funding problems during the activity, problems with supervision being carried out by the health service only once a year and while the output is achieving coverage of the antenatal care service program in The Tojo Una Regency Health Service still has not met the target coverage that has been set due to the lack of optimal input and processes in the antenatal care service program system both at the health service and at the community health center. Conclusion: The evaluation at the Tojo Una-una District Health Service in 2023 is still not going well because the input is still inadequate, the process is still not carried out optimally so that the output to achieve program coverage still does not meet the target coverage that has been set.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">615</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Dewi Sartika&lt;sup&gt;1&lt;/sup&gt;*, Amran Razak&lt;sup&gt;2&lt;/sup&gt;, Muhammad Alwy Arifin&lt;sup&gt;3&lt;/sup&gt;,Balqis&lt;sup&gt;4&lt;/sup&gt;, Muhammad Kardi&lt;sup&gt;5&lt;/sup&gt;, Nurhaedar Jafar&lt;sup&gt;6&lt;/sup&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Masters Student of Health Administration and Policy, Faculty of Public Health, Hasanuddin University, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Health Administration and Policy, Faculty of Public Health, Hasanuddin University, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Health Administration and Policy, Faculty of Public Health, Hasanuddin University, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of nutritional sciences, Faculty of Public Health, Hasanuddin University, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Khairunnisa, Muhammad Faizi</style></author><author><style face="normal" font="default" size="100%">Nur Rochmah</style></author><author><style face="normal" font="default" size="100%">Yuni Hisbiyah</style></author><author><style face="normal" font="default" size="100%">Rayi Kurnia Perwitasari</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Girl with McCune-Albright Syndrome: Case Study</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">706-710</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;McCune-Albright syndrome (MAS) is a rare genetic disease characterized by skeletal, cutaneous, and endocrine system involvement. We report a 6-year-old girl with fibrous dysplasia, café-au-lait macula, and multiple hyperfunctional endocrinopathies. Treatment was palliative, the patient was planned for surgery on bilateral femur fractures and a rehabilitation program.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Case Report</style></work-type><section><style face="normal" font="default" size="100%">706</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Khairunnisa, Muhammad Faizi*, Nur Rochmah,Yuni Hisbiyah, Rayi Kurnia Perwitasari&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;Department of Child Health, Faculty of Medicine, Universitas Airlangga/Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Atheer A. Ali</style></author><author><style face="normal" font="default" size="100%">Enas F. Kadhim</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Histological Characterization of Modified Calcite Paste as Pulpotomy Material in Partially Pulpotomized Rabbit Incisors</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Calcite</style></keyword><keyword><style  face="normal" font="default" size="100%">Calcium carbonate</style></keyword><keyword><style  face="normal" font="default" size="100%">Pulpotomy</style></keyword><keyword><style  face="normal" font="default" size="100%">Rabbit incisor</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">415-421</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; increasing the demand for vital pulp therapy (VPT) as a minimally invasive treatment, evolving the need for bio-inspired capping material to optimize the outcome with more predictable results.&lt;strong&gt; Aim: &lt;/strong&gt;is to evaluate the biological efficacy of modified calcite paste as potential material for pulpotomy in terms of pulpal inflammatory response, dentin bridge formation and morphology. &lt;strong&gt;Methods:&lt;/strong&gt; 24 lower central incisors of New Zealand rabbits were used, subdivided into two groups of 12 teeth according to sacrificing time (1 and 4 weeks), in each group, six teeth were used as the control group, the pulp is traumatically exposed and partially amputated left free of capping material, and six teeth used as the experimental group, were the amputated pulp capped with Modified Calcite (MC) paste, the cavity of both groups sealed with resin modified glass ionomere cement (pulpdent, USA).animal were sacrificed and teeth were collected for histological examination. &lt;strong&gt;Results:&lt;/strong&gt; At 1-week and 4-week periods respectively, both groups showed non-significant differences in inflammatory extent, a highly significant difference in calcific bridge formation (P=0.002) and dentin morphology (P=0.002). The MC group showed faster dentin bridge formation with favourable morphology according to the scoring system in both periods compared to the control group. &lt;strong&gt;Conclusions:&lt;/strong&gt; MC composite is a promising novel pulpotomy material.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">415</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Atheer A. Ali, Enas F. Kadhim*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Oral Diagnosis, College of Dentistry, University of Baghdad, Baghdad, IRAQ.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dianasari</style></author><author><style face="normal" font="default" size="100%">Yunias Setiawati</style></author><author><style face="normal" font="default" size="100%">Royke Tony Kalalo</style></author><author><style face="normal" font="default" size="100%">Atika</style></author><author><style face="normal" font="default" size="100%">Farida Anwari</style></author><author><style face="normal" font="default" size="100%">ASM Morshed</style></author><author><style face="normal" font="default" size="100%">Auliya Yudia Yasyfin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Impact of Natural Products and Mindfulness Practices on Serum Serotonin Levels, Clinical Symptoms, and Mindfulness in Adolescents with ADHD Symptoms</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">CAMM</style></keyword><keyword><style  face="normal" font="default" size="100%">mindfulness</style></keyword><keyword><style  face="normal" font="default" size="100%">serotonin serum</style></keyword><keyword><style  face="normal" font="default" size="100%">SPPAHI</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1389-1395</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Attention Deficit Hyperactivity Disorder (ADHD) is a neurodevelopmental condition marked by impulsivity, hyperactivity, and impaired attention (inattention). Pharmacological treatments are often effective but have limitations, necessitating the exploration of alternative therapies. Interventions based on mindfulness (MBIs) have demonstrated effectiveness in alleviating symptoms of ADHD, but their effects on clinical symptoms, serotonin levels, and mindfulness in adolescents have not been thoroughly studied in Indonesia. This study aimed to evaluate the effectiveness of mindfulness-based interventions on the improvement of clinical symptoms, changes in serum serotonin levels, and mindfulness levels in adolescents with ADHD symptoms. &lt;strong&gt;Methods: &lt;/strong&gt;A true-experimental design with a randomized controlled trial was employed. ADHD symptoms were screened using the Abbreviated Conners’ Teacher Rating Scale (ACTRS) among adolescent students in grades 7 through 9 of junior high school (n = 1067). After meeting all inclusion and exclusion criteria, the study included 28 adolescents aged 12–16 years diagnosed with ADHD, divided into treatment (mindfulness) and control groups. Clinical symptoms were assessed using the SPPAHI questionnaire, mindfulness levels were measured with the CAMM scale, and serum serotonin levels were analyzed pre- and post-intervention. &lt;strong&gt;Results:&lt;/strong&gt; The mindfulness group demonstrated notable reductions in clinical symptoms and mindfulness levels in comparison to the control group. There was no notable difference in serum serotonin levels between the two groups. &lt;strong&gt;Conclusions: &lt;/strong&gt;MBIs effectively reduced ADHD symptoms and increased mindfulness levels in adolescents. No substantial changes were observed in serotonin levels, indicating that mindfulness impacts behavioral and cognitive aspects more than biochemical markers. These findings suggest that mindfulness may be a valuable complementary therapy for ADHD management in adolescents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1389</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Dianasari&lt;sup&gt;1,4&lt;/sup&gt;, Yunias Setiawati&lt;sup&gt;2*&lt;/sup&gt;, Royke Tony Kalalo&lt;sup&gt;2&lt;/sup&gt;, Atika&lt;sup&gt;3&lt;/sup&gt;, Farida Anwari&lt;sup&gt;4&lt;/sup&gt;, ASM Morshed&lt;sup&gt;5&lt;/sup&gt; and Auliya Yudia Yasyfin&lt;sup&gt;6&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Child and Adolescent Psychiatry Resident, Department of Psychiatry, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Child and Adolescent Division, Department of Psychiatry, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Public Health and Preventive Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Lecturer, Faculty of Health and Science, Universitas Anwar Medika, Sidoarjo, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Associate Professor and Head, Department of Psychiatry, Dr. Sirajul Islam Medical College, Dhaka, BANGLADESH.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Faculty of Medicine, Universitas Sebelas Maret, Surakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohamed Zaeim Hafez Ahmed</style></author><author><style face="normal" font="default" size="100%">Muhammad Abdelbaeth Hassan Elfiky</style></author><author><style face="normal" font="default" size="100%">Elsayed Elagamy Elsayed Mohamed</style></author><author><style face="normal" font="default" size="100%">Ramadan Hassan Ibrahim Thabet</style></author><author><style face="normal" font="default" size="100%">Ahmed Mohamed Gad Allah</style></author><author><style face="normal" font="default" size="100%">Ahmed Abdrabo Elshenawy Elsisi</style></author><author><style face="normal" font="default" size="100%">Ahmed Abdel Nasser Ahmed Mohamed</style></author><author><style face="normal" font="default" size="100%">Tarek Shikhon</style></author><author><style face="normal" font="default" size="100%">Mostafa Abo-akrab</style></author><author><style face="normal" font="default" size="100%">Sayed A.M.Mahmoud</style></author><author><style face="normal" font="default" size="100%">Mohamed AbdelAziz Doma</style></author><author><style face="normal" font="default" size="100%">Wael Ahmed Mahmoud Khattab</style></author><author><style face="normal" font="default" size="100%">Khaled Saleh Ali Elhamaky</style></author><author><style face="normal" font="default" size="100%">Mohamed El- Salamoni</style></author><author><style face="normal" font="default" size="100%">Fatma Mahmoud Abdelraheem</style></author><author><style face="normal" font="default" size="100%">Mahmoud Ahmad Mohamed Azab</style></author><author><style face="normal" font="default" size="100%">Mahmoud Ahmad Mohamed Azab6</style></author><author><style face="normal" font="default" size="100%">Mohamed E EL-Refaey</style></author><author><style face="normal" font="default" size="100%">Ahmed A. Abd El-Rhman</style></author><author><style face="normal" font="default" size="100%">Ahmed F. Abdel Ghany</style></author><author><style face="normal" font="default" size="100%">Ghada Adel Hegazy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of Chamomile Leaves extract in Different Doses on Renal Functions and Diabetic indices in Streptozotocin – Induced Diabetic Rat</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chamomile leaves</style></keyword><keyword><style  face="normal" font="default" size="100%">Diabetes mellitus</style></keyword><keyword><style  face="normal" font="default" size="100%">Streptozotocin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1029-1035</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; The prevalence of diabetes among Egyptians is rising. Therefore, there is always a demand for innovative natural medicines. Medicinal plants have long been a significant source in search of novel, effective alternatives for human therapy. Chamomile is one of the most widely used medicinal plants, which may help hyperglycemic patients by lowering blood sugar levels. Objectives: To determine how chamomile extract affects the kidneys when albino male rats with chronic diabetes are induced by streptozotocin (STZ). &lt;strong&gt;Methods:&lt;/strong&gt; The study was conducted in the Al-Azhar Faculty of Medicine (Assiut) pharmacology department animal laboratory. For this investigation, a local strain of fifty adult male albino rats was used as the animal model and weighed 120 to 150 g. In this study, rats were divided into five groups, body weight, and systolic blood pressure was measured, and blood samples were collected for measuring blood glucose and insulin level, HbA1c, Na, K, and renal function tests, and histopathological examination was done. &lt;strong&gt;Results:&lt;/strong&gt; After the study, mean glucose levels, HbA1c, urea, creatinine, K, and systolic blood pressure were significantly decreased in group IV &amp;amp; group V compared to group III. In contrast, body weight serum insulin level and Na increased dramatically in group IV &amp;amp; group V compared to group III.&lt;strong&gt; Conclusion:&lt;/strong&gt; The serum levels of urea and creatinine in diabetic patients may be positively affected by chamomile. Additionally, short-term chamomile uses benefits diabetic individuals by decreasing loss of body weight, lowering HbA1c, and increasing insulin levels.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1029</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Mohamed Zaeim Hafez Ahmed&lt;sup&gt;1*&lt;/sup&gt;, Muhammad Abdelbaeth Hassan Elfiky&lt;sup&gt;1&lt;/sup&gt;, Elsayed Elagamy Elsayed Mohamed&lt;sup&gt;2&lt;/sup&gt;, Ramadan Hassan Ibrahim Thabet&lt;sup&gt;2&lt;/sup&gt;, Ahmed Mohamed Gad Allah&lt;sup&gt;3&lt;/sup&gt;, Ahmed Abdrabo Elshenawy Elsisi&lt;sup&gt;2&lt;/sup&gt;, Ahmed Abdel Nasser Ahmed Mohamed&lt;sup&gt;2&lt;/sup&gt;, Tarek Shikhon&lt;sup&gt;4&lt;/sup&gt;, Mostafa Abo-akrab4, Sayed A.M.Mahmoud&lt;sup&gt;5&lt;/sup&gt;, Mohamed AbdelAziz Doma&lt;sup&gt;5&lt;/sup&gt;, Wael Ahmed Mahmoud Khattab&lt;sup&gt;6&lt;/sup&gt;, Khaled Saleh Ali Elhamaky&lt;sup&gt;7&lt;/sup&gt;, Mohamed El-Salamoni&lt;sup&gt;6&lt;/sup&gt;, Fatma Mahmoud Abdelraheem&lt;sup&gt;8,&lt;/sup&gt; Mahmoud Ahmad Mohamed Azab&lt;sup&gt;6&lt;/sup&gt;, Ashraf Abdel Aty Elshenawy Emara&lt;sup&gt;6&lt;/sup&gt;, Mohamed E EL-Refaey&lt;sup&gt;1&lt;/sup&gt;, Ahmed A. Abd El-Rhman&lt;sup&gt;1&lt;/sup&gt;, Ahmed F. Abdel Ghany&lt;sup&gt;1&lt;/sup&gt;, Ghada Adel&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Faculty of Medicine, Al-Azhar University (Assiut), Assiut, EGYPT.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Andi Muh. Maulana</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Erni Hernawati Purwaningsih</style></author><author><style face="normal" font="default" size="100%">Andon Hestiantoro</style></author><author><style face="normal" font="default" size="100%">Taifo Mahmud</style></author><author><style face="normal" font="default" size="100%">Heri Wibowo</style></author><author><style face="normal" font="default" size="100%">Bambang Pontjo Priosoeryanto</style></author><author><style face="normal" font="default" size="100%">Primariadewi Rustamadji</style></author><author><style face="normal" font="default" size="100%">Numlil Khaira Rusdi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Inhibitory Mechanisms of Soybean Extract on the Development of Breast Cancer Through Modulation of Cellular Immune Response</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Breast cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">CD4+</style></keyword><keyword><style  face="normal" font="default" size="100%">CD8+</style></keyword><keyword><style  face="normal" font="default" size="100%">Cellular immune response</style></keyword><keyword><style  face="normal" font="default" size="100%">Soybean extract</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">01-08</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Breast cancer is the most frequently diagnosed cancer in women worldwide. Consumption of soy products has been reported to reduce the incidence of and mortality rate for some cancers, including breast cancer. However, there are limited &lt;em&gt;in vivo&lt;/em&gt; studies on the inhibitory effect of soybean extracts on breast cancer. &lt;strong&gt;Objectives:&lt;/strong&gt; To examine the effect of soybean extracts on breast cancer cellular immunity and to determine the role of CD4&lt;sup&gt;+&lt;/sup&gt; and CD8&lt;sup&gt;+&lt;/sup&gt; T cells in the development and outcome of breast cancer. &lt;strong&gt;Material and Methods:&lt;/strong&gt; Rat were induced with DMBA 11 times to get a breast cancer model. A soybean extract was given at different doses starting one week before DMBA induction and continued until the end of the study. At the end of the study, peripheral blood was collected, and the lymphocytes were examined using flow cytometry. &lt;strong&gt;Results:&lt;/strong&gt; The phytochemical screening of soybean extract, using the Q-TOF LC/MS method, detected four bioactive components from the isoflavone and saponin groups. The incidence of tumor formation in the NeC, SE-D250, SE-D500, and SE-D1000 groups was 100%, 83%, 33%, and 33%, respectively. The highest proportion of CD4+ T cells was found in the NeC (69.35%), while the lowest was in the SE-D1000 (63.75%). The highest and lowest proportions of CD8+ T cells were found in the SE-D1000 and NeC groups, at 35.95% and 31.15%, respectively. &lt;strong&gt;Conclusions:&lt;/strong&gt; The soybean extract was able to reduce the incidence of breast tumor formation in DMBA-induced rat in a dose-dependent manner. The soy extract group's CD4+/CD8+ ratio was close to that of healthy rats compared to the DMBA-induced group without soy extract. A lowered CD4+/CD8+ ratio is followed by a lower risk of tumor formation.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">01</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Andi Muh. Maulana&lt;sup&gt;1,2&lt;/sup&gt;, Kusmardi Kusmardi&lt;sup&gt;1,3,4,5,&lt;/sup&gt;*, Erni Hernawati Purwaningsih&lt;sup&gt;1,4,6&lt;/sup&gt;, Andon Hestiantoro&lt;sup&gt;1,7&lt;/sup&gt;, Taifo Mahmud&lt;sup&gt;8&lt;/sup&gt;, Heri Wibowo&lt;sup&gt;9&lt;/sup&gt;, Bambang Pontjo Priosoeryanto&lt;sup&gt;10&lt;/sup&gt;, Primariadewi Rustamadji&lt;sup&gt;3&lt;/sup&gt;, Numlil Khaira Rusdi&lt;sup&gt;11&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctoral Program in Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Anatomy, Faculty of Medicine, Universitas Muhammadiyah Purwokerto, Banyumas, Central Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pathological Anatomy, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Drug Development Research Center, Indonesian Medical Education and Research Institute, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Human Cancer Research Center, Indonesian Medical Education and Research Institute, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Medical Pharmaceutical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Obstetrics and Gynecology, Faculty of Medicine, Universitas Indonesia – Dr. Cipto Mangunkusumo National General Hospital, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Department of Pharmaceutical Sciences, Oregon State University, 203 Pharmacy Building, Corvallis, Oregon 97331, UNITED STATES.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Department of Parasitology - Integrated Laboratory, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Division of Veterinary Pathology, School of Veterinary Medicine and Biomedical Sciences, IPB University, Bogor, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Faculty of Pharmacy and Sciences, Universitas Muhammadiyah Prof. DR. Hamka, Jakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Raden Anita Indriyanti</style></author><author><style face="normal" font="default" size="100%">Yuktiana Kharisma</style></author><author><style face="normal" font="default" size="100%">Meta Maulida Damayanti</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mangifera indica Linn. Waste Peel Ethanol Extract on Inducing Citrus amblycarpa Hassk. Ochese Antioxidant Activity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Citrus amblycarpa</style></keyword><keyword><style  face="normal" font="default" size="100%">Mangifera indica</style></keyword><keyword><style  face="normal" font="default" size="100%">Peel Extract</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1010-1014</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Excessive production of reactive oxygen species plays a significant role in the proliferation and evolution of numerous high-risk diseases in humans, the antioxidant capacity of bioactive substances is of immense importance.&lt;em&gt; Mangifera indica&lt;/em&gt; L., a medicinal plant has high bioactive metabolite contents and contributes to several positive biological processes in the plant. &lt;em&gt;Citrus amblycarpa&lt;/em&gt; H.O. contains an excellent source of chemical compounds and the presence of these compounds can be a potential pharmacological activity as antimicrobial, anti-inflammatory, antioxidant, and others. The aim of the study is to assess the effect of &lt;em&gt;Mangifera indica&lt;/em&gt; and &lt;em&gt;Citrus amblycarpa&lt;/em&gt; peel ethanol extract as an antioxidant agents.&lt;strong&gt; Method: &lt;/strong&gt;Phytochemical screening of&lt;em&gt; M. indica&lt;/em&gt; and &lt;em&gt;C. amblycarpa&lt;/em&gt; peeled ethanol extract was done to identify alkaloids, polyphenols, flavonoids, anthraquinone, tannins, and terpenoid contents. The antioxidant activity of the extract was determined using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) method. &lt;strong&gt;Result:&lt;em&gt; &lt;/em&gt;&lt;/strong&gt;&lt;em&gt;Mangifera indica &lt;/em&gt;and &lt;em&gt;Citrus amblycarpa &lt;/em&gt;peel ethanol extract have an antioxidant activity of IC&lt;sub&gt;50&lt;/sub&gt; 29,28 μg/mL and IC&lt;sub&gt;50&lt;/sub&gt; 669,52 μg/mL separately, while combination antioxidant activity was 48,05 μg/ mL. &lt;strong&gt;Conclusion:&lt;/strong&gt; &lt;em&gt;Mangifera indica&lt;/em&gt; Linn. peel ethanol extract could induce &lt;em&gt;Citrus amblycarpa&lt;/em&gt; antioxidant activity producing a potential antioxidant agent.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1010</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Raden Anita Indriyanti&lt;sup&gt;1*&lt;/sup&gt;, Yuktiana Kharisma&lt;sup&gt;2&lt;/sup&gt;, Meta Maulida Damayanti&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Faculty of Medicine, Bandung Islamic University, Bandung, West Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pathology Anatomy, Faculty of Medicine, Bandung Islamic University, Bandung, West Java, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wirda Anggraini</style></author><author><style face="normal" font="default" size="100%">Djoko Agus Purwanto</style></author><author><style face="normal" font="default" size="100%">Idha Kusumawati</style></author><author><style face="normal" font="default" size="100%">Isnaeni</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mechanism and Antifungal Activities Vulvovaginal Candidiasis Isolated from Patients Against Ethanol Extracts of Parameria laevigata (Juss.) Moldenke Stem Bark</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Candida albicans</style></keyword><keyword><style  face="normal" font="default" size="100%">Compound</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Microdilution method</style></keyword><keyword><style  face="normal" font="default" size="100%">Ultrasound Assisted Extraction</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">684-688</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Fungal diseases are not an exception to the current antibiotic resistance situation. Antimicrobial stewardship programs and high drug screening are two of the measures that are being used. Today, fungal infections are severe health problems. Utilizing plant-based natural compounds that are effective against various human pathogenic fungi is one method for preventing the issues associated with fungal infection. In this research, extracts are used as an option to treat patients with Candida albicans infection. The research aimed to examine the antifungal properties of an ethanol extract from Parameria laevigata (Juss.) Moldenke stem bark against C. albicans isolated from patients. &lt;strong&gt;Methods:&lt;/strong&gt; This research used a microdilution method. C. albicans from patients diagnosed with vulvovaginal candidiasis. The test sample is 70% and 96% ethanol extracted from P. laevigata stem bark. Data analysis used One-way ANOVA with a P value of 0.000. &lt;strong&gt;Results:&lt;/strong&gt; The result showed that PLE-70 can inhibit the growth of C. albicans with the highest %inhibition for ATCC 14053, CP-1, CP-2, CP-3, and CP-4, respectively 36.39%; 37.51%; 38.66%; 45.78%; 84.87%. PLE-96 can inhibit the growth of C. albicans with the highest %inhibition for ATCC 14053, CP-1, CP-2, CP-3, and CP-4 respectively 17.49%; 17.77%; 29.27%; 34.12%; 38.42%. Conclusion: It was concluded that the ethanol extract from P. laevigata stem bark can inhibit C. albicans isolated from vulvovaginal candidiasis patients.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">684</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Wirda Anggraini&lt;sup&gt;1,4&lt;/sup&gt;, Djoko Agus Purwanto&lt;sup&gt;2&lt;/sup&gt;*, Idha Kusumawati&lt;sup&gt;2&lt;/sup&gt;, Isnaeni&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Doctor of Pharmaceutical Sciences, Faculty of Pharmacy, Airlangga University, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Sciences, Faculty of Pharmacy, Airlangga University, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacy, Faculty of Health Science, Muhammadiyah University Surabaya, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacy, Faculty Medicine and Health Sciences, Maulana Malik Ibrahim State Islamic University Malang, Malang, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohammed Saarti</style></author><author><style face="normal" font="default" size="100%">Musab M Khalaf</style></author><author><style face="normal" font="default" size="100%">Zeina A. Althanoon</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Non-Nutritive Sweeteners Modulated Creatinine and Urea Levels in White Albino Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acesulfame-K</style></keyword><keyword><style  face="normal" font="default" size="100%">Artificial Sweeteners</style></keyword><keyword><style  face="normal" font="default" size="100%">Aspartame</style></keyword><keyword><style  face="normal" font="default" size="100%">Non-nutritive sweeteners</style></keyword><keyword><style  face="normal" font="default" size="100%">Saccharine</style></keyword><keyword><style  face="normal" font="default" size="100%">Sucralose</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">422-425</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Artificial sweeteners, also known as nonnutritive sweeteners have many benefits like low calories count. It is frequently used for reducing weight, controlling blood sugar levels and decreasing the chances of dental decay. This study evaluated the effects of NNS in the kidney function. Using the blood sample of the albino rats, the level of creatinine and urea was calculated after the use of NNS for 3 weeks. 70 rats were equally divided into 7 groups. The groups were given Stevia 200mg/kg/day, 10% solution of sucrose, Sucralose 3g/kg/day, Saccharine, Aspartame 250mg/kg/day and Acesulfame-k 250mg/kg/day respectively. In the controlled group, distilled water was used as a placebo. The results indicated that saccharin and aspartame both caused the urea to increase to 37±0.5 mg/dl from initial 30±1.5mg/dl and acesulfame-k represented the most increase in the urea, which elevated the levels from 30 mg/dl to 38±1.5 mg/dl. Additionally, saccharine and aspartame increased the creatinine levels from from 0.1 to 0.85±0.05 mg/ dl and sucralose elevated the level of creatinine from 0.1 mg/dl to 1.3±0.2 mg/dl. In the stevia group, the results remained the same as in the controlled group. This indicates the nephrotoxic effects of NNS and proves Stevia safe for the daily use as an alternative.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">422</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Mohammed Saarti, Musab M Khalaf, Zeina A. Althanoon*&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;Department of Pharmacology and Toxicology, College of Pharmacy, University of Mosul, Mosul, IRAQ.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mirawati Tongko</style></author><author><style face="normal" font="default" size="100%">Yahya Thamrin</style></author><author><style face="normal" font="default" size="100%">Syamsiar S. Russeng</style></author><author><style face="normal" font="default" size="100%">Lalu Muhammad Saleh</style></author><author><style face="normal" font="default" size="100%">Sukri Palutturi</style></author><author><style face="normal" font="default" size="100%">Ridwan Amiruddin</style></author><author><style face="normal" font="default" size="100%">Irwandy</style></author><author><style face="normal" font="default" size="100%">Anwar Mallongi</style></author><author><style face="normal" font="default" size="100%">Maria Kanan</style></author><author><style face="normal" font="default" size="100%">Fahrudin Lahay</style></author><author><style face="normal" font="default" size="100%">Almustari</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Occupational Diseases in Female Workers in the Industrial World, Indonesia: Hazard Types and Exposure Mechanisms – Literature Review</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Female Worker</style></keyword><keyword><style  face="normal" font="default" size="100%">Hazard</style></keyword><keyword><style  face="normal" font="default" size="100%">Industry</style></keyword><keyword><style  face="normal" font="default" size="100%">Occupational Disease</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">263-267</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Occupational diseases are diseases caused by work and the work environment. Specifically gender, women have a double burden, namely domestic work in the household and the burden of being a breadwinner who works outside the home, women are also faced with reproductive tasks, namely pregnancy, childbirth and breastfeeding, and bioanatomically women have physical strength different from men, so that women are specifically more vulnerable to health risks due to their work, both physically, mental and social. This research will review the types and mechanisms of the spread of Occupational Diseases (OD) in female workers in the industrial world. &lt;strong&gt;Methods: &lt;/strong&gt;The writing of this research was carried out using the Literature Review method which is a literature review method in which scientific articles are selected by researchers related to the research topic. &lt;strong&gt;Results:&lt;/strong&gt; According to the results of the study, the specific risk of occupational diseases in the female worker community is pregnancy and childbirth disorders, Anemia and Sexuall Transmitted Disease (STD), while other accompanying diseases are Pulmonary Obstruction Disease, Tinea pedis, Neurotoksic Symptoms, Noice Induce Hearing Loss (NIHL), Low Back Pain (LBP), MSDs, and Work Stress. &lt;strong&gt;Conclusion:&lt;/strong&gt; Every female worker has a susceptibility to occupational diseases according to the conditions and work environment experienced. The industry must pay attention to programs to improve occupational health by making anticipatory efforts so that occupational diseases do not become a life threat to female workers.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">263</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Mirawati Tongko&lt;sup&gt;1,&lt;/sup&gt;*, Yahya Thamrin&lt;sup&gt;1&lt;/sup&gt;, Syamsiar S. Russeng&lt;sup&gt;1&lt;/sup&gt;, Lalu Muhammad Saleh&lt;sup&gt;1&lt;/sup&gt;, Sukri Palutturi&lt;sup&gt;2&lt;/sup&gt;, Ridwan Amiruddin&lt;sup&gt;2&lt;/sup&gt;, Irwandy&lt;sup&gt;3&lt;/sup&gt;, Anwar Mallongi&lt;sup&gt;4&lt;/sup&gt;, Maria Kanan&lt;sup&gt;5&lt;/sup&gt;, Fahrudin Lahay&lt;sup&gt;6&lt;/sup&gt;, Almustari&lt;sup&gt;7&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Occupational Health and Safety, Faculty of Public Health Hasanuddin University, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Epidemiology, Faculty of Public Health, Hasanuddin University, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Hospital Management and Administration, Faculty of Public Health,&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohammad Anam Al Arif</style></author><author><style face="normal" font="default" size="100%">Sunaryo Hadi Warsito</style></author><author><style face="normal" font="default" size="100%">Mirni Lamid</style></author><author><style face="normal" font="default" size="100%">Widya Paramita Lokapirnasari</style></author><author><style face="normal" font="default" size="100%">Aswin Rafif Khairullah</style></author><author><style face="normal" font="default" size="100%">Siti Rani Ayuti</style></author><author><style face="normal" font="default" size="100%">Sugito</style></author><author><style face="normal" font="default" size="100%">Intan Permatasari Hermawan</style></author><author><style face="normal" font="default" size="100%">Oky Setyo Widodo</style></author><author><style face="normal" font="default" size="100%">Rakhi Gangil</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Analysis of Curry Leaf Extract (Murraya koenigii L.) as a Potential Animal Feed and Medicinal Ingredient</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Curry leaf extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Human health</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">471-477</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Herbal plants have been used for centuries as traditional medicine to treat various diseases. Green plants generally contain phytochemical compounds, such as vegetables and plants that add aroma to dishes, one of which is curry leaves (Murraya Koenigii). This research aims to identify the phytochemical compounds contained in curry leaves. This research was carried out from August 2023 to October 2023. The curry leaves that were obtained were converted into extract form and then the extract was tested for the content of alkaloids, flavonoids, saponins, phenolics and tannins. The research results showed that curry leaf extract contained 23.73% alkaloids, 1.24% flavonoids, 8.74% saponins, 4.4% phenolics, and 5.2% tannins. Alkaloids in plants have a role as a defense against biotic and abiotic disorders. The benefits of flavonoids in plants include anti-mutagenic, anti-inflammatory, antioxidant and anti-carcinogenic. Saponins have various benefits in the health sector, including being able to reduce cholesterol concentrations in the blood. Polyphenols have good antioxidant power because this group can provide electrons to neutralize free radical electrons formed in the body. Tannins also consist of polyphenolic compounds which have antibacterial, antioxidant and astringent activities. The results of the analysis regarding the content of secondary metabolite compounds in curry leaf extract play an important role in the development of future medicines and need to be carried out to provide knowledge to the public. This study can be a basis for bioactive content for further research to expand the use of medicinal plants in the future, especially curry plants.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">471</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Mohammad Anam Al Arif&lt;sup&gt;1&lt;/sup&gt;, Sunaryo Hadi Warsito&lt;sup&gt;1&lt;/sup&gt;, Mirni Lamid&lt;sup&gt;1*&lt;/sup&gt;, Widya Paramita Lokapirnasari&lt;sup&gt;1&lt;/sup&gt;, Aswin Rafif Khairullah&lt;sup&gt;2&lt;/sup&gt;, Siti Rani Ayuti3, Sugito&lt;sup&gt;3&lt;/sup&gt;, Intan Permatasari Hermawan&lt;sup&gt;4&lt;/sup&gt;, Oky Setyo Widodo&lt;sup&gt;1,5&lt;/sup&gt;, Rakhi Gangil&lt;sup&gt;6&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Animal Husbandry, Faculty of Veterinary Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Research Center for Veterinary Science, National Research and Innovation Agency, Bogor, INDONESIA&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Veterinary Medicine, Universitas Syiah Kuala, Aceh, INDONESIA&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Faculty of Veterinary Medicine, Universitas Wijaya Kusuma, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;5&lt;/sup&gt;Laboratory of Theriogenology Joint Faculty of Veterinary Medicine, Faculty of Veterinary Medicine, Yamaguchi University, Yamaguchi, JAPAN.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Veterinary Microbiology, College of Veterinary Science and AH MHOW, Nanaji Deshmukh Veterinary University Jabalpur, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sarath Lal P S</style></author><author><style face="normal" font="default" size="100%">Thirumal M</style></author><author><style face="normal" font="default" size="100%">Ajith Babu T K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical and Pharmacological Studies of Different Extracts of Stem Bark and Leaf of Flueggea leucopyrus Willd.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Extraction</style></keyword><keyword><style  face="normal" font="default" size="100%">Flueggea leucopyrus</style></keyword><keyword><style  face="normal" font="default" size="100%">In vitro anti-inflammatory activity</style></keyword><keyword><style  face="normal" font="default" size="100%">In vitro antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical evaluation</style></keyword><keyword><style  face="normal" font="default" size="100%">Spectral evaluation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1281-1289</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Traditional medicinal plants are generally extracted and evaluated to identify potential sources of effective drugs. Objective: The present study aimed to conduct the phytochemical and pharmacological evaluation of stem bark and leaf extracts of &lt;em&gt;Flueggea leucopyrus&lt;/em&gt;. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The collected plant material was dried, powdered, and extracted separately by soxhlation with different solvents viz., petroleum ether, n-hexane, chloroform, acetone, methanol, and water. All the extracts were subjected to phytochemical evaluation. Alkaloids were extracted and characterized from the powdered sample of leaf and bark. &lt;em&gt;In vitro&lt;/em&gt; antioxidant activity of the extracts was evaluated by DPPH (2, 2-diphenyl-1-picrylhydrazyl) and nitric oxide radical scavenging assay and anti-inflammatory activity by inhibition of protein denaturation and Human red blood cell (HRBC) membrane stabilization method. &lt;strong&gt;Results: &lt;/strong&gt;Extracts were found to be either semisolid or solid with different tints of green or brown colour. The preliminary phytochemical evaluation found alkaloids, glycoside, phenolic compounds, flavonoids, carbohydrates, sterol, and saponin. On spectral evaluation, the presence of an alkaloid, Securinol-A was found in a fraction extracted from the bark. In the &lt;em&gt;in vitro&lt;/em&gt; antioxidant and anti-inflammatory activity the tested samples showed a concentration-dependent rise of activity, particularly, the isolated fraction and acetone extract of stem bark revealed a significant activity. &lt;strong&gt;Conclusion:&lt;/strong&gt; Alkaloids, flavonoids, sterols, and saponins identified in these extracts may be responsible for these biological activities. Hopefully, our&lt;em&gt; in vitro&lt;/em&gt; and in &lt;em&gt;vivo &lt;/em&gt;evaluations&lt;em&gt; &lt;/em&gt;and compound-level studies in the future will reveal significant data for the development of clinically useful chemotherapeutic agents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1281</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sarath Lal P S&lt;sup&gt;1&lt;/sup&gt;, Thirumal M&lt;sup&gt;2*&lt;/sup&gt;, Ajith Babu T K&lt;sup&gt;3&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Research Scholar, Department of Pharmacognosy, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chengalpattu District-603203, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Associate Professor, Department of Pharmacognosy, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chengalpattu District-603203, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Professor &amp;amp; Principal, Malik Deenar College of Pharmacy, Seethangoli, Kasaragod, Kerala, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Okram Ronibala Devi</style></author><author><style face="normal" font="default" size="100%">Lutrika Moirangthem</style></author><author><style face="normal" font="default" size="100%">Ojit Singh Keithellakpam</style></author><author><style face="normal" font="default" size="100%">Nanaocha Sharma</style></author><author><style face="normal" font="default" size="100%">Kshetrimayum Birla Singh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Screening and Evaluation of Antioxidant Potential in Euryale ferox Salisb. and Eupatorium birmanicum DC. of Manipur, India</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoid</style></keyword><keyword><style  face="normal" font="default" size="100%">Foxnut</style></keyword><keyword><style  face="normal" font="default" size="100%">Northeast India</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenol</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1231-1237</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Euryale ferox Salisb. popularly called “Foxnut” is a spiny aquatic plant locally named “Thangjing” in Manipur and is one of the most highly consumed aquatic crops while &lt;em&gt;Eupatorium birmanicum&lt;/em&gt; DC. locally named “Langthrei” is an endemic ethnomedicinal plant found in Manipur, India. &lt;strong&gt;Methods: &lt;/strong&gt;This study was carried out to examine the phytochemical content, evaluate the Total Phenolic Content (TPC), Total Flavonoid Content (TFC) and the in vitro antioxidant potential (DPPH and ABTS assays) in the seeds, arils of &lt;em&gt;E. ferox&lt;/em&gt; and leaves of &lt;em&gt;E. birmanicum.&lt;/em&gt; &lt;strong&gt;Results: &lt;/strong&gt;Phytochemicals such as phenols, flavonoids, saponins, tannins, alkaloids and steroids were detected from the plant samples studied. Among the samples, TPC was found in the range 21.95 ± 1.18 mgGAE/g ext to 119.80 ± 2.63 mgGAE/g ext while, TFC was recorded in the range 2.57 ± 0.07 mgQE/g ext to 7.27 ± 0.28 mgQE/g ext with the highest value of TPC and TFC in &lt;em&gt;E. ferox &lt;/em&gt;seeds. In case of DPPH and ABTS assays, the recorded IC&lt;sub&gt;50&lt;/sub&gt; value were attained in the range 16.99 ± 0.49 μg/mL to 335.90 ± 2.19 μg/mL and 70.69 ± 1.83 μg/mL to 576.26 ± 4.41 μg/mL respectively with the lowest IC&lt;sub&gt;50&lt;/sub&gt; value recorded in &lt;em&gt;E. ferox&lt;/em&gt; seeds. &lt;strong&gt;Conclusions:&lt;/strong&gt; The results of our study revealed that seeds and arils of &lt;em&gt;E. ferox&lt;/em&gt; as well as leaves of &lt;em&gt;E. birmanicum &lt;/em&gt;contain a variety of phytochemicals and promising antioxidant activity which will contribute a scientific insight for exploration of their therapeutic potentials in the future.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1231</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Okram Ronibala Devi&lt;sup&gt;1&lt;/sup&gt;, Lutrika Moirangthem&lt;sup&gt;2&lt;/sup&gt;, Ojit Singh Keithellakpam&lt;sup&gt;3&lt;/sup&gt;, Nanaocha Sharma&lt;sup&gt;3&lt;/sup&gt;, Kshetrimayum Birla Singh&lt;sup&gt;1,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Zoology, Manipur University, Canchipur, Imphal, Manipur, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;²Department of Biochemistry, Manipur University, Canchipur, Imphal, Manipur, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;³Animal Bioresources Division, Institute of Bioresources and Sustainable Development, Takyelpat, Imphal, Manipur, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sabrina Chris Janiba Sanvee</style></author><author><style face="normal" font="default" size="100%">Bignoate Kombate</style></author><author><style face="normal" font="default" size="100%">Yendubé Toughelighan Kantati</style></author><author><style face="normal" font="default" size="100%">Pascaline Kindji Kpoyizoun</style></author><author><style face="normal" font="default" size="100%">Essotolom Badjabaissi</style></author><author><style face="normal" font="default" size="100%">Mindede Assih1 Aboudoulatif Diallo</style></author><author><style face="normal" font="default" size="100%">Batomayena Bakoma</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemistry, Antihyperglycemic, Antioxidant and Anti- Inflammatory Properties of Uvaria Chamae and Sida Linifolia Extracts: Potential Implication in Diabetic Disease</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Decoction</style></keyword><keyword><style  face="normal" font="default" size="100%">hyperglycemia</style></keyword><keyword><style  face="normal" font="default" size="100%">Neuroprotection</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemistry</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">582-590</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Uvaria chamae and Sida linifolia are plants traditionally used in Togo in diabetes treatment, an affection that often leads to several complications. This study aimed to evaluate the antihyperglycemic, anti-inflammatory, antioxidant activity and toxicity of these two plants extracts.&lt;strong&gt; Methods:&lt;/strong&gt; A phytochemical analysis was carried out on extracts obtained either by decoction or maceration in ethanol of Uvaria chamae leaves and Sida linifolia whole plant. Evaluation of the antihyperglycemic activity consisted in glucose absorption test using yeast and rats’ muscle and jejunum. DPPH test, total antioxidant capacity assay, hemolysis and egg albumin denaturation inhibition assays and evaluation of extracts acute toxicity were performed. &lt;strong&gt;Results: &lt;/strong&gt;Hydroalcoholic extract of Uvaria chamae showed the strongest antihyperglycemic activity (p&amp;lt;0.05); the highest phenolic contents (147.93 ± 1.01 mg/g), the best total antioxidant capacity (153.33 ± 4.07), the lowest IC50 (μg/mL) for DPPH test (296.96 ± 91.69), a capacity of hemolysis (825.99 ± 29.24) and egg albumin denaturation (738.10 ± 92.26) inhibition assays. In the same way, hydroalcoholic extract of Sida linifolia, showed the strongest antihyperglycemic activity (p&amp;lt;0.05), the highest phenolic contents (71.60 ± 2.16 mg/g), the best total antioxidant capacity (146.98 ± 2.81), lowest IC50 (μg/ mL) for DPPH test (788.28 ± 112.54), the hemolysis (882.03 ± 20.86) and egg albumin denaturation (1966.18 ± 35.94) inhibition assays. None of the extracts showed acute toxicity in rats. &lt;strong&gt;Conclusion: &lt;/strong&gt;the hydroalcoholic leaves extract of Uvaria chamae and of the whole plant of Sida linifolia could be candidates in the treatment of diabetes and its complications.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">582-590</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Sabrina Chris Janiba Sanvee&lt;sup&gt;1&lt;/sup&gt;*, Bignoate Kombate², Yendubé Toughelighan Kantati², Pascaline Kindji Kpoyizoun², Essotolom Badjabaissi&lt;sup&gt;1&lt;/sup&gt;, Mindede Assih&lt;sup&gt;1&lt;/sup&gt; Aboudoulatif Diallo&lt;sup&gt;1&lt;/sup&gt; Batomayena Bakoma&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Laboratory of Pharmaceutical Science, Faculty of Health Sciences, University of Lomé, Lomé- Togo, 01BP 1515, LOME.&lt;/p&gt;

&lt;p&gt;²Laboratory of Physiology/Pharmacology, Physiopathology Bioactive Substances and Innocuity Research Unit (PBSI), Faculty of Sciences, University of Lomé, Lomé - Togo, 01BP 1515. LOME.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ruqiah Ganda Putri Panjaitan</style></author><author><style face="normal" font="default" size="100%">Titin</style></author><author><style face="normal" font="default" size="100%">Yohanes Gatot Sutapa Yuliana</style></author><author><style face="normal" font="default" size="100%">Siti Khotimah</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Plants with Antidiabetic Efficacy among the Dayak Bidayuh Community, Sanggau Regency, West Kalimantan, Indonesia</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Dayak Bidayuh Tribe</style></keyword><keyword><style  face="normal" font="default" size="100%">Diabetes mellitus</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal plants</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">1342-1348</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The use of medicinal plants for diabetes mellitus has been practiced for generations by the Dayak communities in West Kalimantan, Indonesia. The aim of this study is to inventory and describe the utilization of medicinal plants for diabetes mellitus by the Dayak Bidayuh Kerambay, Dayak Golik, and Dayak Sinangkan’t communities in Sekayam, Beduai, and Entikong Districts, Sanggau Regency, West Kalimantan, Indonesia. &lt;strong&gt;Method:&lt;/strong&gt; This research is a qualitative descriptive study using triangulation method combining interview, observation, and documentation techniques of anti-diabetic mellitus medicinal plants among the Dayak communities. &lt;strong&gt;Results: &lt;/strong&gt;The plants used as anti-diabetic mellitus include Physalis angulata L.,&lt;em&gt; Ageratum&lt;/em&gt; &lt;em&gt;conyzoides &lt;/em&gt;L., &lt;em&gt;Piper betle&lt;/em&gt; L.,&lt;em&gt; Dillenia suffruticosa&lt;/em&gt; (Griff.) Martelli, &lt;em&gt;Syzygium polyanthum&lt;/em&gt; (Wight) Walp. &lt;em&gt;Stenochlaena palustris&lt;/em&gt; (Burm.f.) Bedd, &lt;em&gt;Gynura procumbens&lt;/em&gt; (Lour.) Merr, &lt;em&gt;Curcuma domestica Valeton&lt;/em&gt;,&lt;em&gt; Zingiber officinale Rosc&lt;/em&gt;., &lt;em&gt;Eleutherine palmifolia&lt;/em&gt; (L.) Merr, &lt;em&gt;Curcuma zedoaria&lt;/em&gt; (Christm.) Roscoe, &lt;em&gt;Orthosiphon stamineus&lt;/em&gt; B., &lt;em&gt;Nepenthes&lt;/em&gt; sp., &lt;em&gt;Solanum torvum&lt;/em&gt; Swartz, &lt;em&gt;Garcinia mangostana &lt;/em&gt;L. The plant parts most commonly used, in sequence, are leaves, rhizomes, roots, fruits, fruit peels, and sometimes the entire plant. The method of preparation for each type of plant is the same, which involves boiling and consuming the boiled decoction. &lt;strong&gt;Summary: &lt;/strong&gt;There are 15 types of plants used by the Dayak tribe community to address diabetes mellitus. Among these 15 types of plants, different parts are utilized, while the processing method remains the same, which is boiling.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1342</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ruqiah Ganda Putri Panjaitan&lt;sup&gt;1*&lt;/sup&gt;, Titin&lt;sup&gt;1&lt;/sup&gt;, Yohanes Gatot Sutapa Yuliana&lt;sup&gt;2&lt;/sup&gt;, Siti Khotimah&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Biology Education Program, Faculty of Teacher Training and Education, Tanjungpura University, Prof. Dr. H. Hadari Nawawi Street, Bansir Laut, Southeast Pontianak District, Pontianak City, West Kalimantan 78124, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;English Language Education Program, Faculty of Teacher Training and Education, Tanjungpura University, Prof. Dr. H. Hadari Nawawi Street, Bansir Laut, Southeast Pontianak District, Pontianak City, West Kalimantan 78124, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Biology Study Program, Faculty of Mathematics and Natural Sciences, Tanjungpura University, Prof. Dr. H. Hadari Nawawi Street, Bansir Laut, Southeast Pontianak District, Pontianak City, West Kalimantan 78124, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Novi Fajar Utami</style></author><author><style face="normal" font="default" size="100%">Berna Elya</style></author><author><style face="normal" font="default" size="100%">Hayun Hayun</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Quantification of Active Compounds from Coffea canephora Pierre ex A.Froehner cascara and their Potential Against MCF-7 and HeLa</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Breast cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Cascara</style></keyword><keyword><style  face="normal" font="default" size="100%">Coffea canephora</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxic</style></keyword><keyword><style  face="normal" font="default" size="100%">Isolation</style></keyword><keyword><style  face="normal" font="default" size="100%">servical cancer</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">509-518</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;The utilization of coffee cascara, a byproduct of coffee cultivation, in cancer therapy research. This research begins with the rationale of exploring medicinal plants, especially coffee, to obtain compounds that can target cancer cells with fewer side effects. &lt;strong&gt;Objectivity: &lt;/strong&gt;This research aims to extract and evaluate the secondary metabolites from robusta coffee cascara, such as friedelin, lupeol, stigmasterol, ursolic acid, caffeine, chlorogenic acid, caffeic acid, and catechin, for their cytotoxic activity against Hela and MCF-7 cells. The aim of this research is also to identify and understand the cytotoxic mechanisms of compounds like stigmasterol, which showed significant cytotoxicity against cancer cells, paving the way for developing targeted cancer therapies from natural sources. &lt;strong&gt;Methods:&lt;/strong&gt; Robusta coffee cascara then goes to the process of extraction using ethanol, fractionation, isolation, purification, and characterization, followed by bioactivity evaluation using in vitro method through breast cancer cell line MCF-7 and cervical cancer cell line HeLa and determination of active compound levels. &lt;strong&gt;Results:&lt;/strong&gt; The cascara, a byproduct of coffee cultivation, is rich in proteins, polysaccharides, and bioactive compounds. Through extraction and purification processes, eight compounds were isolated and characterized, including &lt;strong&gt;(1)&lt;/strong&gt; friedelin, &lt;strong&gt;(2)&lt;/strong&gt; lupeol,&lt;strong&gt; (3)&lt;/strong&gt; Stigmasterol, &lt;strong&gt;(4)&lt;/strong&gt; Ursolic acid, &lt;strong&gt;(5)&lt;/strong&gt; caffeine, &lt;strong&gt;(6)&lt;/strong&gt; Chlorogenic acid, &lt;strong&gt;(7)&lt;/strong&gt; caffeic acid, and &lt;strong&gt;(8)&lt;/strong&gt; catechin. Bioactivity evaluation shows that stigmasterol (3) is the most cytotoxic compound with a value against Hela cells with an IC50 value of 25.85 μg/mL in the toxic category and against MCF-7 cells with an IC50 value of 12.83 μg/mL in the very toxic category. The results of determining the levels of active compounds in robusta coffee cascara extract showed that friedelin &lt;strong&gt;(1)&lt;/strong&gt; 0.539±0.137%; lupeol &lt;strong&gt;(2)&lt;/strong&gt; levels were 0.087±0.015%; &lt;strong&gt;(3)&lt;/strong&gt; stigmasterol 0.126±0.046%; ursolic acid &lt;strong&gt;(4)&lt;/strong&gt; 0.627±0.002%; caffeine &lt;strong&gt;(5) &lt;/strong&gt;3,203±0.069%; chlorogenic acid &lt;strong&gt;(6)&lt;/strong&gt; 0.679±0.003%; caffeic acid &lt;strong&gt;(7) &lt;/strong&gt;0.153±0.003% and catechin &lt;strong&gt;(8)&lt;/strong&gt; 0.3590.012% mg/g extract. &lt;strong&gt;Conclusion:&lt;/strong&gt; The research on robusta coffee cascara extract as a potential source of anticancer compounds.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">509</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Novi Fajar Utami&lt;sup&gt;1,2&lt;/sup&gt;, Berna Elya&lt;sup&gt;1&lt;/sup&gt;*, Hayun Hayun&lt;sup&gt;3&lt;/sup&gt;, Kusmardi Kusmardi&lt;sup&gt;4,5,6&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Phytochemistry and Pharmacognosy, Faculty of Pharmacy, Universitas Indonesia, Depok 16424 West Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Math and Science, Universitas Pakuan, Jl. Raya Pakuan 1 Bogor, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Pharmacy, Universitas Indonesia, Depok 16424 West Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Anatomic Pathology, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya No.6, Jakarta, 10430, Jakarta, Indonesia, 10430 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Drug Development Research Cluster, Indonesia Medical Educational and Research Institute, Jl. Salemba Raya No.6, Jakarta 10340, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Human Cancer Research Cluster, Indonesia Medical Educational and Research Institute, Jl. Salemba Raya No.6, Jakarta 10340, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Junjungan Kristianto Manurung</style></author><author><style face="normal" font="default" size="100%">Prananda Surya Airlangga</style></author><author><style face="normal" font="default" size="100%">Hamzah Hamzah</style></author><author><style face="normal" font="default" size="100%">Prihatma Kriswidyatomo</style></author><author><style face="normal" font="default" size="100%">Anggraini Dwi Sensusiati</style></author><author><style face="normal" font="default" size="100%">Budi Utomo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Relationship Between Blood Levels of Ubiquitin Carboxyterminal Hydrolase L1 (UCH-L1) Protein and the Severity of Traumatic Brain Injury Based on the Glasgow Coma Scale and Rotterdam CT Score</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Glasgow Coma Scale</style></keyword><keyword><style  face="normal" font="default" size="100%">Rotterdam CT score</style></keyword><keyword><style  face="normal" font="default" size="100%">Traumatic Brain Injury</style></keyword><keyword><style  face="normal" font="default" size="100%">UCH-L1</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">695-699</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; Traumatic brain injury (TBI) is a leading cause of disability and death worldwide, with an estimated 64-74 million cases annually. The current gold standard for diagnosis is a computed tomography (CT) scan, which has limitations such as access, cost, and radiation risk. Therefore, a simple, accessible, and safe diagnostic modality is needed, one of which is biomarker examination. This study aims to establish the relationship between blood levels of the biomarker ubiquitin carboxy-terminal hydrolase-L1 (UCH-L1) and the severity of TBI based on the Glasgow Coma Scale (GCS) and Rotterdam CT score. &lt;strong&gt;Material and Methods: &lt;/strong&gt;This observational analytic study with a cross-sectional design involved 41 samples aged 18-50 years who presented to the Emergency Department of Dr. Soetomo General Hospital, Surabaya, within 3-24 hours of the incident. UCH-L1 levels were measured from blood samples using the ELISA method, and the data on UCH-L1, GCS, and Rotterdam CT scores were analyzed with SPSS 29. &lt;strong&gt;Results:&lt;/strong&gt; The mean UCH-L1 level was 0.522 ± 0.592, with a cutoff value of &amp;gt; 0.2057, indicating moderate to severe TBI if UCH-L1 levels exceeded 0.2057. Spearman's test and correlation coefficient analysis showed a strong relationship between UCH-L1 levels and Rotterdam CT score (p &amp;lt; 0.05), as well as between UCH-L1 levels and TBI severity based on GCS (p &amp;lt; 0.05). The cutoff value for Rotterdam CT score was &amp;gt; 2, indicating moderate to severe TBI if the score exceeded 2. &lt;strong&gt;Conclusion:&lt;/strong&gt; Serum UCH-L1 levels are significantly associated with the severity of TBI based on GCS and Rotterdam CT score.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">695</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Junjungan Kristianto Manurung&lt;sup&gt;1&lt;/sup&gt;, Prananda Surya Airlangga&lt;sup&gt;1&lt;/sup&gt;*, Hamzah Hamzah&lt;sup&gt;1&lt;/sup&gt;, Prihatma Kriswidyatomo&lt;sup&gt;1&lt;/sup&gt;, Anggraini Dwi Sensusiati&lt;sup&gt;2&lt;/sup&gt;, Budi Utomo&lt;sup&gt;3&lt;/sup&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anesthesiology and Intensive Care, Faculty of Medicine, Universitas Airlangga – Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Radiology, Faculty of Medicine, Universitas Airlangga – Airlangga University Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Departement of Public Health &amp;amp; Preventive Medicine, Faculty of Medicine, Universitas Airlangga – Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rian Nofiansyah</style></author><author><style face="normal" font="default" size="100%">Kohar Hari Santoso</style></author><author><style face="normal" font="default" size="100%">Prananda Surya Airlangga</style></author><author><style face="normal" font="default" size="100%">Prihatma Kriswidyatomo</style></author><author><style face="normal" font="default" size="100%">Hamzah</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Relationship Between Cerebrospinal Fluid S100B Levels with Glasgow Coma Scale and Rotterdam CT Score in Traumatic Brain Injury Patients</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Glasgow Coma Scale</style></keyword><keyword><style  face="normal" font="default" size="100%">Rotterdam CT score.</style></keyword><keyword><style  face="normal" font="default" size="100%">S100B</style></keyword><keyword><style  face="normal" font="default" size="100%">Traumatic Brain Injury</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">503-508</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;!-- x-tinymce/html --&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Traumatic brain injury (TBI) stands as one of the foremost reasons for mortality and incapacitation in young adults on a global scale, accounting for nearly half of all injury-related deaths. The severity of TBI can be assessed using various biomarkers, with the SI00B protein being one of them. While many studies have explored the correlation between serum protein levels and various aspects such as neuroimaging findings, clinical scores, and neuropsychological evaluations, there is a notable lack of research examining the correlation with cerebrospinal fluid (CSF) levels. &lt;strong&gt;Methods: &lt;/strong&gt;The research design of this study was prospective and observational, employing analytic methods for analysis. Fifteen TBI patients who met the inclusion and exclusion criteria and were fitted with ICP monitors comprised the study sample. GCS data used is post-resuscitation GCS. Data on SIOOB protein levels were taken from the examination of CSF samples taken when the ICP monitor was installed. Rotterdam CT score variables was taken from the last CT scan performed before the patient was fitted with an ICP monitor. The statistical analysis was conducted utilizing the SPSS version 26 software. &lt;strong&gt;Results: &lt;/strong&gt;Demographic characteristics for this study tended to be more male (73.3%), with ages ranging from 18 to 65 years, and a mean age of 34.60 ± 16.22 years. The majority of injury mechanisms were traffic accidents (80%), and the most common lesion type was ICH. The mean CSF S 100B value of the 15 samples was 2753.689 pg/ ml. The results of the relationship test between S 100B CSF and GCS using the Spearman test obtained a p-value of less than 0.05, indicating a meaningful correlation between S 100B CSF and GCS, with a correlation coefficient or r value of -0.684. The results of the SIOOB CSF relationship test with Rotterdam CT Score obtained a p-value &amp;lt;0.05, with a correlation coefficient or r value of 0.827. &lt;strong&gt;Conclusion: &lt;/strong&gt;Increased levels of S100B in cerebrospinal fluid are associated with decreased GCS and increased Rotterdam CT score in traumatic brain injury patients.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">503</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Rian Nofiansyah&lt;sup&gt;1&lt;/sup&gt;*, Kohar Hari Santoso&lt;sup&gt;2&lt;/sup&gt;, Prananda Surya Airlangga&lt;sup&gt;2&lt;/sup&gt;, Prihatma Kriswidyatomo&lt;sup&gt;2&lt;/sup&gt;, Hamzah&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Clinical Medicine Study Program, Master’s Degree, Faculty of Medicine, Universitas Airlangga – Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Anesthesiology and Reanimation, Faculty of Medicine, Universitas Airlangga – Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wibowo Artho Sutrisno</style></author><author><style face="normal" font="default" size="100%">Prananda Surya Airlangga</style></author><author><style face="normal" font="default" size="100%">Citrawati Dyah Kencono Wungu</style></author><author><style face="normal" font="default" size="100%">Prihatma Kriswidyatomo</style></author><author><style face="normal" font="default" size="100%">Hamzah</style></author><author><style face="normal" font="default" size="100%">Bambang Pujo Semedi</style></author><author><style face="normal" font="default" size="100%">Mahmudah</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Role of Neuron Specific Enolase, S100B, Glial Fibrillary Acidic Protein, and Myelin Basic Protein as Prognostic and Survival Values in Traumatic Brain Injury: Systematic Review and Meta-analysis</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Glial Fibriallary Acidic Protein</style></keyword><keyword><style  face="normal" font="default" size="100%">Myelin Basic Protein</style></keyword><keyword><style  face="normal" font="default" size="100%">Neuron Specific Enolase</style></keyword><keyword><style  face="normal" font="default" size="100%">Prognostic Value</style></keyword><keyword><style  face="normal" font="default" size="100%">S100B</style></keyword><keyword><style  face="normal" font="default" size="100%">Survival</style></keyword><keyword><style  face="normal" font="default" size="100%">Traumatic Brain Injury</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">478-484</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;The high number of accidents and traumatic brain injuries, especially in the productive age group, causes a lot of morbidity and mortality. A fast and accurate examination method is needed for the diagnosis and treatment of traumatic brain injury. Nerve damage biomarkers such as Neuron Specific Enolase, S100B, Glial Fibrillary Acidic Protein, and Myelin Basic Protein, have been used globally both for research and daily use to determine the severity of traumatic brain injury. &lt;strong&gt;Methods:&lt;/strong&gt; Searches and journal searches were carried out from Science Direct, Scopus, Springer Link, and PubMed, with the keywords &quot;Neuron Specific Enolase&quot;, &quot;S100B&quot;, &quot;Glial Fibrillary Acidic Protein&quot;, &quot;Myelin Basic Protein&quot;, and &quot;Traumatic Brain Injury ”. Screening was carried out using PRISMA 2021 to look for studies that met the criteria and were of sufficient study quality according to the Newcastle-Ottawa Scale. &lt;strong&gt;Results: &lt;/strong&gt;Twenty-three studies were collected and further grouped based on outcomes, both prognostic and survival outcomes. Neuron Specific Enolase, S100B, and Glial Fibrillary Acidic Protein values were higher in poor outcomes (all p values &amp;lt; 0.001) and poor survival (all p values &amp;lt; 0.001) in traumatic brain injury. Myelin Basic Protein was not significant in poor outcome (p = 0.35), but was higher in poor survival (p &amp;lt; 0.001) in traumatic brain injury. &lt;strong&gt;Conclusion:&lt;/strong&gt; Neuron Specific Enolase, S100B, and Glial Fibrillary Acidic Protein, can be used as markers for prognostic and survival value in traumatic brain injury. Myelin Basic Protein can be used as a marker for survival value in traumatic brain injury.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">478</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Wibowo Artho Sutrisno&lt;sup&gt;1&lt;/sup&gt;, Prananda Surya Airlangga&lt;sup&gt;1*&lt;/sup&gt;, Citrawati Dyah Kencono Wungu&lt;sup&gt;2&lt;/sup&gt;, Prihatma Kriswidyatomo&lt;sup&gt;1&lt;/sup&gt;, Hamzah1, Bambang Pujo Semedi&lt;sup&gt;1&lt;/sup&gt;, Mahmudah&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anesthesiology and Reanimation, Faculty of Medicine, Airlangga University - Dr Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Physiology and Medical Biochemistry, Faculty of Medicine, Airlangga University, Surabaya, INDONESIA. 3Department of Community Health, Faculty of Community Health, Airlangga University, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Henu Hadiyantama</style></author><author><style face="normal" font="default" size="100%">Lukisiari Agustini</style></author><author><style face="normal" font="default" size="100%">Sutjipto</style></author><author><style face="normal" font="default" size="100%">Evelyn Komaratih</style></author><author><style face="normal" font="default" size="100%">Ismi Zuhria</style></author><author><style face="normal" font="default" size="100%">Pudji Lestari</style></author><author><style face="normal" font="default" size="100%">Ridholia</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Role of α-SMA, Type 1 Collagen, and Myofibroblasts in Cicatrizing Conjunctivitis by Alkali Chemical Trauma</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cicatrizing conjunctivitis</style></keyword><keyword><style  face="normal" font="default" size="100%">Myofibroblasts</style></keyword><keyword><style  face="normal" font="default" size="100%">Type 1 collagen</style></keyword><keyword><style  face="normal" font="default" size="100%">α -SMA</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">591-596</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Chemical trauma to the eye is a serious condition in the field of ophthalmology and a leading factor contributing to global blindness. Cicatrizing conjunctivitis (CC) is a term used to describe conditions marked by inflammation and the formation of scars on the conjunctiva. CC can have various causes, with one of them being chemical injury to the eye. The development of CC involves the participation of several cytokines and cells, such as α-SMA, Type 1 collagen, and Myofibroblasts. Myofibroblasts have the ability to contract through the utilization of diverse cytoskeletal proteins, which are commonly present in smooth muscle cells, including α-SMA. Actin filaments contribute to mechanically supporting cells, defining cell morphology, and facilitating cell mobility. Actin, in conjunction with myosin, participates in the muscle contraction process within muscle cells. Subsequently, type 1 collagen contributes to the healing of conjunctival wounds by providing a tensile force that aids in the closure of such wounds. As a significant constituent of the extracellular matrix, type 1 collagen plays a crucial role in maintaining the integrity of tissues.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">591</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Henu Hadiyantama&lt;sup&gt;1&lt;/sup&gt;, Lukisiari Agustini&lt;sup&gt;1*&lt;/sup&gt;, Sutjipto&lt;sup&gt;1&lt;/sup&gt;, Evelyn Komaratih&lt;sup&gt;1&lt;/sup&gt;, Ismi Zuhria&lt;sup&gt;1&lt;/sup&gt;, Pudji Lestari&lt;sup&gt;2&lt;/sup&gt;, Ridholia&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Ophthalmology, Faculty of Medicine, Universitas Airlangga/Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Public Health, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA. 3Department of Pathology Anatomy, Faculty of Medicine/Dr. Soetomo General Academic Hospital, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Piracha Jumpa-ngern</style></author><author><style face="normal" font="default" size="100%">Parunkul Tungsukruthai</style></author><author><style face="normal" font="default" size="100%">Chuntida Kamalashiran</style></author><author><style face="normal" font="default" size="100%">Somboon Kietinun</style></author><author><style face="normal" font="default" size="100%">Kesara Na- Bangchang</style></author><author><style face="normal" font="default" size="100%">Kusuma Sriyakul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Safety Assessment of Oral Lysiphyllum strychnifolium Aqueous Extract in Healthy Volunteers</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Clinical study</style></keyword><keyword><style  face="normal" font="default" size="100%">Healthy volunteers</style></keyword><keyword><style  face="normal" font="default" size="100%">Lysiphyllum strychnifolium</style></keyword><keyword><style  face="normal" font="default" size="100%">Safety</style></keyword><keyword><style  face="normal" font="default" size="100%">Yanang Daeng</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">235-240</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Lysiphyllum strychnifolium&lt;/em&gt; (LS), widely known as Ya nang daeng in Thailand, is a traditional herbal remedy that has long been used to promote health and treat diverse health conditions, especially detoxification, by alleviating the severity of symptoms and lowering the risks associated with toxic exposures. Although it is extensively used in Thailand, human safety studies have been lacking. Thus, this study aimed to examine the safety of using LS capsules in healthy participants through a Phase I clinical trial. &lt;strong&gt;Objective:&lt;/strong&gt; This study aimed to investigate the safety of aqueous extract of LS in twenty-four healthy Thai participants. &lt;strong&gt;Method: &lt;/strong&gt;The participants were received 1,000 mg of LS aqueous extract each morning before their meals for seven days. All participants were examined safety assessment including history taking, physical examination, and laboratory tests at day 0, 8 and 14 (follow-up). &lt;strong&gt;Results:&lt;/strong&gt; The findings showed that there were no significant side effects or abnormalities found during the history taking, physical examination, or laboratory evaluation. Particularly, when compared to baseline, participants who received LS experienced statistically significant reductions in blood sugar, triglyceride, LDL cholesterol, and creatinine (P &amp;lt; 0.05), but still within normal ranges. &lt;strong&gt;Conclusions:&lt;/strong&gt; Dietary supplementation with 1,000 mg of LS aqueous extract per day may have a beneficial effect on blood sugar and cholesterol management while remaining safe for healthy people.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">235</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Piracha Jumpa-ngern&lt;sup&gt;1&lt;/sup&gt;, Parunkul Tungsukruthai&lt;sup&gt;1&lt;/sup&gt;, Chuntida Kamalashiran&lt;sup&gt;1&lt;/sup&gt;, Somboon Kietinun&lt;sup&gt;1&lt;/sup&gt;, Kesara Na-Bangchang&lt;sup&gt;2,3&lt;/sup&gt;, Kusuma Sriyakul&lt;sup&gt;1,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Integrative Medicine, Chulabhorn International College of Medicine, Thammasat University, Pathumthani 12120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Graduate Program in Bioclinical Sciences, Chulabhorn International College of Medicine, Thammasat. University, Pathum Thani 12120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Drug Discovery and Development Center, Office of Advanced Science and Technology, Thammasat University, Pathumthani 12120, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Intanri Kurniati</style></author><author><style face="normal" font="default" size="100%">Agustyas Tjiptaningrum</style></author><author><style face="normal" font="default" size="100%">Raja Iqbal Mulya Harahap</style></author><author><style face="normal" font="default" size="100%">Bayu Putra Danan Jaya</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Serum Trace Element Levels in Type 2 DM Patients and its Correlation with Glycemic Control</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Fasting blood glucose</style></keyword><keyword><style  face="normal" font="default" size="100%">glycemic control</style></keyword><keyword><style  face="normal" font="default" size="100%">HbA1c</style></keyword><keyword><style  face="normal" font="default" size="100%">trace element serum</style></keyword><keyword><style  face="normal" font="default" size="100%">Type 2 diabetes mellitus</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">660-663</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Type 2 diabetes mellitus, a chronic metabolic disorder, is known to impact serum trace element levels. Objectives: to investigates the association between serum trace elements (Co, Cr, and Cu) and glycemic control in individuals with type 2 diabetes. &lt;strong&gt;Material and Methods:&lt;/strong&gt; A 209 type 2 diabetes patients from Dr. H. Abdul Moeloek Hospital in Bandar Lampung and Hasan Sadikin Hospital in Bandung participated in the study. Patients underwent assessments for serum trace element levels (Co, Cr, and Cu) and glycemic control indicators (FBG and HbA1c). &lt;strong&gt;Results:&lt;/strong&gt; Results indicated significantly lower Co levels in uncontrolled diabetes versus controlled cases (P&amp;lt;0.05). Co, Cr, and Cu levels displayed a significant negative correlation with HbA1c (P&amp;lt;0.05), while Cr and Cu showed a significant negative correlation with FBG (P&amp;lt;0.05). Age did not show significant correlations with serum trace element levels. &lt;strong&gt;Conclusion:&lt;/strong&gt; serum trace element levels (Co, Cr, Cu) are inversely linked to glycemic control in type 2 diabetes individuals.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">660</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Intanri Kurniati&lt;sup&gt;1&lt;/sup&gt;*, Agustyas Tjiptaningrum&lt;sup&gt;1&lt;/sup&gt;, Raja Iqbal Mulya Harahap&lt;sup&gt;2&lt;/sup&gt;, Bayu Putra Danan Jaya&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Clinical Pathology, Faculty of Medicine, Universitas Lampung, Bandar Lampung, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Clinical Pathology, Faculty of Medicine, Universitas Padjajaran – Hasan Sadikin Hospital, Bandung, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Histology and Pathology Laboratory, Faculty of Medicine, Universitas Lampung, Bandar Lampung, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jane Wanja Mbiri</style></author><author><style face="normal" font="default" size="100%">Kenneth Ogila</style></author><author><style face="normal" font="default" size="100%">Patrick Kisangau</style></author><author><style face="normal" font="default" size="100%">Michael Gicheru</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Acute and Sub-acute Oral Toxicity Profile of Root Bark Methanol Extract of Carissa Edulis Vahl</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biochemical parameters</style></keyword><keyword><style  face="normal" font="default" size="100%">Body weights</style></keyword><keyword><style  face="normal" font="default" size="100%">hematological parameters</style></keyword><keyword><style  face="normal" font="default" size="100%">Organ weights.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">253-258</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Carissa edulis is widely used in traditional medicine to manage numerous ailments. However, few studies have assessed its toxicity. Therefore, this study aimed to determine acute and sub-toxicity levels of&lt;em&gt; C. edulis &lt;/em&gt;methanol extract. &lt;strong&gt;Methods:&lt;/strong&gt; In the acute toxicity probe, a limit test was conducted whereby the extract was given as a solo dose by gavage. The rats were observed for two weeks. The observations included mortality and changes in the general appearance and behavior of the experimental animals. The body weights of the rats were taken weekly. For the sub-acute toxicity probe, the rats received the extract daily at dosages 300, 520, and 900 mg/kg by gavage for 28 days. Body weights were also taken weekly. On day twenty-nine, the weights of the rats were taken, the rats were sacrificed, and blood was collected for biochemical and hematological analysis. Body organs were harvested, and their weights were taken. &lt;strong&gt;Results: &lt;/strong&gt;The results of the acute toxicity probe showed that the extract didn’t cause mortality or toxicity signs throughout the study duration. The LD50 of the extract was therefore deemed to be above 2,000 mg/kg. The sub-acute toxicity probe results demonstrated that the extract, at all the tested dosages, didn’t cause mortality or affect the rats’ organ weights, body weights, or hematological and biochemical parameters throughout the study duration. &lt;strong&gt;Conclusions&lt;/strong&gt;: In conclusion, the methanol extract of &lt;em&gt;C. edulis&lt;/em&gt; is not toxic since it didn’t cause mortality or toxicity signs in both acute and sub-acute toxicity probes.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">253</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Jane Wanja Mbiri&lt;sup&gt;1,*&lt;/sup&gt;, Kenneth Ogila&lt;sup&gt;1&lt;/sup&gt;, Patrick Kisangau&lt;sup&gt;2&lt;/sup&gt;, Michael Gicheru&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Jomo Kenyatta University of Agriculture and Technology, Department of Zoology, P.O. Box 43844-00100, Nairobi, KENYA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;South Eastern Kenya University, Department of Life Sciences, P.O Box 170-90200, Kitui, KENYA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Kenyatta University, Department of Zoology, P.O. Box 43844-00100, Nairobi, KENYA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Martohap Parotua Lumbanraja</style></author><author><style face="normal" font="default" size="100%">Kusnandar Anggadiredja</style></author><author><style face="normal" font="default" size="100%">Hubbi Nashrullah Muhammad</style></author><author><style face="normal" font="default" size="100%">Neng Fisheri Kurniati</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Alkaloids from Pandanus amaryllifolius Roxb Leaf as Promising Candidates for Antidyslipidemic Agents: An in silico study</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alkaloids</style></keyword><keyword><style  face="normal" font="default" size="100%">Dyslipidemia</style></keyword><keyword><style  face="normal" font="default" size="100%">In Silico.</style></keyword><keyword><style  face="normal" font="default" size="100%">Pandan</style></keyword><keyword><style  face="normal" font="default" size="100%">Pandanus amaryllifolius</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">106-111</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The plant &lt;em&gt;Pandanus amaryllifolius &lt;/em&gt;Roxb (pandan), has been shown to have antidyslipidemic potency. This study explored the potential of several alkaloids from pandan leaf as antidyslipidemia as well as their safety profile &lt;em&gt;in silico&lt;/em&gt;. &lt;strong&gt;Methods:&lt;/strong&gt; Analyses were carried out by studying the binding affinity of the alkaloids to 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, peroxisome proliferator activator receptor (PPAR) alpha and Niemann Pick C1 Like 1 (NPC1L1). The structures of the alkaloids were downloaded from the Pubchem database and optimized using the ChemDraw Professional 16.0 to obtain 3D structures in protein data bank (PDB) format. The&lt;em&gt; in silico &lt;/em&gt;testing was based on the interactions of the alkaloids with the HMG-CoA reductase (PDB ID 1HW9), PPAR alpha (PDB ID 6LX4) and NPC1L1 (PDB ID 7DFZ) proteins, downloaded from the Research Collaboratory for Structural Bioinformatics (RSCB) PDB website (http://www.rcsb.org/pdb). The preparation of protein structures was performed using the Discovery studio 2021 client and Gromacs applications, while optimization of the 3D structure of the alkaloids was carried out with the ChemDraw professional 16.0. Finally, validation was completed using AutoDock application. The safety profile was assessed by pkCSM online tool.&lt;strong&gt; Results&lt;/strong&gt;: The respective root mean square deviation (RMSD) values of the 1HW9, 6LX4 and 7DFZ proteins were 1.677, 0.918 and 1.706, respectively. The alkaloids pandanusine B, pandamarilactonine A, pandamarilactonine B had respective values of binding energy for HMG-CoA of -5.52, -5.51 and -5.46 kcal/mol. The binding energy of pandamarilactonine B, pandamarilactonine A and pandanamine for PPAR alpha were -9.14, -9.10 and -8.48 kcal/mol, respectively, with the corresponding energy for t NPC1L1 of -9.63, -9.71 and -8.54 kcal/mol. The toxicity tests indicated that the alkaloids were safe, pandamarilactonines had the highest LD&lt;sub&gt;50&lt;/sub&gt; (2.736 mol/ kg). &lt;strong&gt;Conclusion:&lt;/strong&gt; The studied pandan alkaloids have potential antidyslipidemic activity by interacting with HMG-CoA reductase, PPAR alpha, and NPC1L1, with good safety profile.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">106</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Martohap Parotua Lumbanraja, Kusnandar Anggadiredja*, Hubbi Nashrullah Muhammad, Neng Fisheri Kurniati&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Pharmacology and Clinical Pharmacy, School of Pharmacy Institut Teknologi Bandung, Jl. Ganesa 10 Bandung 40132, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Faradila Kilkoda</style></author><author><style face="normal" font="default" size="100%">Balqis</style></author><author><style face="normal" font="default" size="100%">Indar</style></author><author><style face="normal" font="default" size="100%">Darmawansyah</style></author><author><style face="normal" font="default" size="100%">Atjo Wahyu</style></author><author><style face="normal" font="default" size="100%">Anwar Daud</style></author><author><style face="normal" font="default" size="100%">Anwar Mallongi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Analysis Factors Affecting the Utilization of Antiretroviral Treatment Services in HIV Patients in Ambon City Puskesmas</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">AIDS</style></keyword><keyword><style  face="normal" font="default" size="100%">ARV</style></keyword><keyword><style  face="normal" font="default" size="100%">HIV</style></keyword><keyword><style  face="normal" font="default" size="100%">Puskesmas</style></keyword><keyword><style  face="normal" font="default" size="100%">Utilization</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">424-428</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Acquired Immune Deficiency Syndrome (AIDS) is a collection of symptoms that arise due to decreased immunity caused by HIV infection. Human Immunodeficiency Virus (HIV) is a type of virus that infects white blood cells which causes a decrease in human immunity. Efforts are being made at this time for people with HIV namely Antiretroviral treatment (ARV). This study aims to analyze the factors that influence the utilization of ARV treatment services in HIV patients at the Ambon City Health Center. This type of research is a quantitative analytic study with a cross sectional design. Respondents in this study were obtained using the Isaac and Michael method of 156 HIV patients from the Waihaong Health Center and Karpan Health Center in Ambon City using a questionnaire. Data processing was carried out using SPSS and for data analysis using statistical tests using descriptive statistical tests, comparative analysis tests and multivariate analysis tests. The results showed that there was no effect of knowledge on the use of ARV treatment in HIV patients at the Ambon City Health Center. Furthermore, there is an influence on the patient's actions, access distance, and peer and community support on the use of ARV treatment in HIV patients at the Ambon City Health Center. The action variable and access distance are the variables that have the strongest influence compared to the other variables.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">424</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Faradila Kilkoda&lt;sup&gt;1,*&lt;/sup&gt;, Balqis&lt;sup&gt;2&lt;/sup&gt;, Indar&lt;sup&gt;2&lt;/sup&gt;, Darmawansyah&lt;sup&gt;2&lt;/sup&gt;, Atjo Wahyu&lt;sup&gt;3&lt;/sup&gt;, Anwar Daud&lt;sup&gt;4&lt;/sup&gt;, Anwar Mallongi&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Students of the Postgraduate Study Program in Public Health, Faculty of Public Health, Hasanuddin University, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Health Administration and Policy, Faculty of Public Health, Hasanuddin University, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Departement of Occupational Safety and Health, Faculty of Public Health, Hasanuddin University INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Environmental Health, Faculty of Public Health, Hasanuddin University, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hartono Kahar</style></author><author><style face="normal" font="default" size="100%">Sari Prabandari Prasetyaningrum</style></author><author><style face="normal" font="default" size="100%">Munawaroh Fitriah</style></author><author><style face="normal" font="default" size="100%">Aryati</style></author><author><style face="normal" font="default" size="100%">Jusak Nugraha</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Analysis of Covid-19 Neutralizing Antibody Levels Post Vaccination using Ichroma™ and iFlash Covid-19 Nab</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ichroma</style></keyword><keyword><style  face="normal" font="default" size="100%">iFlash.</style></keyword><keyword><style  face="normal" font="default" size="100%">Neutralizing Antibody</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">171-174</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; One of the efforts to control SARS-CoV-2 infection in health workers is vaccination. In this study, the levels of SARS-CoV-2 neutralizing antibody (nAb) in health workers were measured with Ichroma and iFlash. &lt;strong&gt;Methods:&lt;/strong&gt; This study applied an observational analytic design with a prospective cohort and was conducted at Dr. Soetomo Regional Public Hospital, Surabaya, from January to November 2021. The population of this study included a total of 75 health workers after taking the second dose of the SARS-CoV-2 (Sinovac) vaccine. The Covid-19 NAb levels of the population were tested with Ichroma and iFlash on day 0 before vaccination, as well as days 14 and 28, and months 3 and 6 after vaccination. &lt;strong&gt;Results: &lt;/strong&gt;The Friedman test indicated a significant difference in NAb levels according to the iFlash test on day 14, day 28, month 3, and month 6 compared to those before vaccination (p &amp;lt; 0.05). The Wilcoxon test revealed a significant difference in NAb levels on day 14, day 28, month 3, and month 6. The results of the Cochran test showed a significant difference in the positivity of NAb according to the Ichroma test on day 14, day 28, month 3, and month 6 compared to those before vaccination (p &amp;lt; 0.05). McNemar's test demonstrated that the COI at month 3 was not significantly different from that before vaccination; The COI at month 6 was not significantly different from those at days 14 and 28. The results of the Pearson correlation test and Bland–Altman plot indicated a moderate correlation between Ichroma and iFlash (r = 0.592, p = 0.002).&lt;strong&gt; Conclusion:&lt;/strong&gt; Neutralizing antibodies for Covid-19 were formed after day 14 and started to increase on day 28 and started to decrease in months 3 and 6. The levels of NAb for Covid-19 were measured with Ichroma and iFlash in roughly the same pattern and had a moderate positive correlation.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">171</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Hartono Kahar&lt;sup&gt;1,*&lt;/sup&gt;, Sari Prabandari Prasetyaningrum&lt;sup&gt;2&lt;/sup&gt;, Munawaroh Fitriah&lt;sup&gt;2&lt;/sup&gt;, Aryati&lt;sup&gt;2&lt;/sup&gt;, Jusak Nugraha&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Laboratory Instalation, Dr. Soetomo Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Clinical Pathology Specialization Program, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fares Khenniche</style></author><author><style face="normal" font="default" size="100%">Abderachid Slimani</style></author><author><style face="normal" font="default" size="100%">Chawki Bensouici</style></author><author><style face="normal" font="default" size="100%">Ibtissem Magboune</style></author><author><style face="normal" font="default" size="100%">Manel Srief</style></author><author><style face="normal" font="default" size="100%">Hamed Hakkom</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative and Evaluative Study On Total Phenolic Content and Antioxidant Potential Within Hydromythanol Extracts and Their Fractions from All Parts of Drimia numidica (JORD. &amp; FOURR.) J.C. MANNING &amp; GOLDBLATT of Northeastern Algeria</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Drimia numidica</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydromythanol extracts and their fractions.</style></keyword><keyword><style  face="normal" font="default" size="100%">total phenolic content</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">64-81</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;&lt;em&gt;Drimia numidica&lt;/em&gt; is a polyphenol-rich species that has antioxidant capacity, which makes it very important. Nevertheless, &lt;em&gt;D. numidica&lt;/em&gt; has not been studied in depth. Moreover, its capsules have not been studied so far. This detailed study compared the values of total phenolic content and antioxidant activity of all &lt;em&gt;D. numidica&lt;/em&gt; parts (scapes, flowers, bulbs, capsules, leaves, roots), from Edough Peninsula, Annaba, Algeria, using hydromethanol extracts and their fractions (cyclohexane, chloroform, ethyl acetate, and n-butanol). &lt;strong&gt;Methods&lt;/strong&gt;: The total phenolic content was determined by Folin Ciocalteo assay, and the antioxidant activity by the following methods: DPPH, Reducing Powder, Phenanthroline, Silver Nanoparticles, CUPRAC, and ABTS. Statistical analysis was done using the ANOVA test and a correlation test (between antioxidant activity and total phenolic content). &lt;strong&gt;Results: &lt;/strong&gt;The Ethyl acetate fraction was found the sample with the highest phenolic content. The same was true for the antioxidant activity in all tests except for the silver nanoparticles test in which cyclohexane extracts scored the best. Considering the methods used in general, there is a correlation between phenolic content and the highest antioxidant activity, but there are some methods that have not recorded any correlation. &lt;strong&gt;Conclusion: &lt;/strong&gt;Choosing the appropriate method or extract/fraction type is extremely important. In addition, extracts of &lt;em&gt;D. numidica &lt;/em&gt;parts could be an important natural alternative to antioxidants industrial.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">64</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Fares Khenniche&lt;sup&gt;1,*&lt;/sup&gt;, Abderachid Slimani&lt;sup&gt;1&lt;/sup&gt;, Chawki Bensouici&lt;sup&gt;2&lt;/sup&gt;, Ibtissem Magboune&lt;sup&gt;2&lt;/sup&gt;, Manel Srief&lt;sup&gt;2,3&lt;/sup&gt;, Hamed Hakkom&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Laboratory of Plant Biology and Environnement «Médicinal Plants» Axis, Faculty of Sciences, University Badji Mokhtar- Annaba. BP 12, 23000 Annaba, ALGERIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Biotechnology Research Center, Ali Mendjeli UV 3, PBOX 73, El Khroub, Constantine, ALGERIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Biotechnology laboratory, National Higher School of Biotechnology, Constantine, ALGERIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">S. Nithya</style></author><author><style face="normal" font="default" size="100%">S. Dhanalakshmi</style></author><author><style face="normal" font="default" size="100%">S. Anand Babu</style></author><author><style face="normal" font="default" size="100%">S. Nirmala</style></author><author><style face="normal" font="default" size="100%">D. Bharathi</style></author><author><style face="normal" font="default" size="100%">L. Karpagavalli</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Study of Polyherbal Formulation for Antiarthritic Activity Having Cockle Shell, Egg Shell, Ginger and Balloon Vein in Gel Form and Oil Form: A Novel Preparation for Anti-Oxidant Activity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Herb formulation</style></keyword><keyword><style  face="normal" font="default" size="100%">In vitro studies – DPPH.</style></keyword><keyword><style  face="normal" font="default" size="100%">RA</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">714-718</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Inflammatory and chronic disease of the joints and tissues surrounding them, rheumatoid arthritis is known as the most common form of arthritis. Traditional medicines plays major role because of more advantageous like lesser side effects, naturally available and cost effective. A formulation for anti arthritis activity was developed, isolated, and evaluated in this study. Based on the extensive review of the literature, we have formulated three formulation like gel, polyherbal oil formulation with extract of herbs and polyherbal formulation with powders of herbs. We have selected, traditional herbs (Cockle shell, Egg shell, Ginger and Ballon Vein) based on the literature and does a comparative study between gel and the oil formulation to check which has better anti arthritis activity. The selected herbs for formulation of gel are cockle shell and egg shell which has rich calcium content and for oil formulation herbs like ballon vein and ginger were chosen.The chemical constituent present in herbs plays a major role in curing rheumatoid arthritis.Then finally we have done a evaluation like ph measurement, spreadability, specific gravity, antioxidant study etc., between the comparison of DPPH assay of the formulation, clearly reported that the efficacy in the medicated oil in the extract and well in the macerated oil showed significant antioxidant activity when compared to the gel.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">714</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;S. Nithya&lt;sup&gt;1,*&lt;/sup&gt;, S. Dhanalakshmi&lt;sup&gt;2&lt;/sup&gt;, S. Anand Babu&lt;sup&gt;2&lt;/sup&gt;, S. Nirmala&lt;sup&gt;3&lt;/sup&gt;, D. Bharathi&lt;sup&gt;4&lt;/sup&gt;, L. Karpagavalli&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Faculty of Pharmacy, Sri Ramachandra Institute of Higher Education and Research, Chennai, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacognosy, Department of Pharmaceutics, GRT Institute of Pharmaceutical Education and Research, Tiruttani, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacognosy, Faculty of Pharmacy, Sree Balaji Medical College and Hospital campus, Bharath Institute of Higher Education and Research, Chromepet, Chennai, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmaceutical chemistry, Jaya college of Pharmacy, Chennai, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Emranul Kabir</style></author><author><style face="normal" font="default" size="100%">M. R. O. Khan Noyon</style></author><author><style face="normal" font="default" size="100%">Monir Uzzaman</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Computational and Pharmacokinetic Investigation of Some Heterocyclic Amide Derivatives as Cyclooxygenase Inhibitors: An In-Silico Approach</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ADMET.</style></keyword><keyword><style  face="normal" font="default" size="100%">Cyclooxygenase (COX)</style></keyword><keyword><style  face="normal" font="default" size="100%">Heterocyclic amide derivatives</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">194-207</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The two most significant as well as historically important non-steroidal and anti-inflammatory medications (NSAIDs), aspirin and ibuprofen, are frequently used to treat fever, pain, and inflammation. By blocking the activity of cyclooxygenase (COX), it can prevent the production of prostaglandin. In an effort to examine the physiochemical and biological properties of some heterocyclic amide derivatives and quantum mechanical computations have been used to analyze the compounds. To clarify the thermochemical, molecular orbital, and equilibrium geometrical features in the gas phase, density functional theory (DFT) with the B3LYP/6- 31G basis set has been used. Binding affinities and modes of heterocyclic amide analogs have been investigated on human cyclooxygenase (COX-1 and COX-2) proteins (6Y3C and 5F19) using molecular docking as well as nonbonding interactions. Results from geometry and thermochemical analysis support the chemical sustainability of all the structures. Most of the compounds exhibited a significant affinity for binding to the receptor protein (5F19) than the standard drugs aspirin and ibuprofen. The improved pharmacokinetic features of certain derivatives with reduced acute oral toxicity were revealed by ADMET prediction. Overall, four heterocyclic amide analogs 3-6 were found to be more efficient in inhibiting COX- 2 (5F19) than COX-1 (6Y3C), suggesting that they may be useful as COX-2-related inflammation drug candidates.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">194</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Emranul Kabir&lt;sup&gt;1,2*&lt;/sup&gt;, M. R. O. Khan Noyon&lt;sup&gt;1&lt;/sup&gt;, Monir Uzzaman&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry, Faculty of Science, University of Chittagong, Chittagong-4331, BANGLADESH.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Electrical and Electronic Engineering, Faculty of Science, International Islamic University, Chittagong- 4318, BANGLADESH.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Rismi Verawati</style></author><author><style face="normal" font="default" size="100%">Rauza Sukma Rita</style></author><author><style face="normal" font="default" size="100%">Fadhli Ranuharja</style></author><author><style face="normal" font="default" size="100%">Musa Ghufron</style></author><author><style face="normal" font="default" size="100%">Agariadne Dwinggo Samala</style></author><author><style face="normal" font="default" size="100%">Herland Satriawan</style></author><author><style face="normal" font="default" size="100%">Muhammad Raffi Ghifari</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Amalia Putri Lubis</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Computational Evaluation of the Potential of Salicylate Compound from Syzygium aromaticum on Carbonic Anhydrase I as a Gastric Acid Stimulant</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Carbonic Anhydrase I</style></keyword><keyword><style  face="normal" font="default" size="100%">Gastric Acid Stimulant</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword><keyword><style  face="normal" font="default" size="100%">Salicylate</style></keyword><keyword><style  face="normal" font="default" size="100%">Syzygium Aromaticum.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">489-493</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This article explores the potential of the salicylate compound (&lt;em&gt;Syzygium Aromaticum&lt;/em&gt;) as a stimulant for Carbonic Anhydrase I in gastric acid secretion, using a computational approach. The research methods include molecular modeling with Pymol and Pyrex, determination of compound structure and interactions with Protein Plus, and examination of physicochemical properties using the Lipinski Rule. The results show that the Binding Affinity of salicylate with Carbonic Anhydrase I ranges from -7.3 to -6.5, with RMSD values of 0, 2.102, and 2.212, indicating good modeling quality. The interaction between salicylate and Carbonic Anhydrase I is also supported by the findings from Protein Plus. Furthermore, the salicylate compound complies with the Lipinski Rule, with a molecular weight of 137, 1 hydrogen bond donor, 3 hydrogen bond acceptors, a log P value of 0.34, and a molar reactivity of 34.16. This study highlights the prospect of salicylate as a potential modulator of Carbonic Anhydrase I.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">489</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Rahadian Zainul&lt;sup&gt;1,2,*&lt;/sup&gt;, Rismi Verawati&lt;sup&gt;1&lt;/sup&gt;, Rauza Sukma Rita&lt;sup&gt;3&lt;/sup&gt;, Fadhli Ranuharja&lt;sup&gt;4&lt;/sup&gt;, Musa Ghufron&lt;sup&gt;5&lt;/sup&gt;, Agariadne Dwinggo Samala&lt;sup&gt;6&lt;/sup&gt;, Herland Satriawan&lt;sup&gt;7&lt;/sup&gt;, Muhammad Raffi Ghifari&lt;sup&gt;8&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;9&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;10&lt;/sup&gt;, Amalia Putri Lubis&lt;sup&gt;1&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;11,12&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;13&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;14,15&lt;/sup&gt;, ANM Ansori&lt;sup&gt;11,12,13&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biochemistry, Faculty of Medicine, Universitas Andalas, Padang, INDONESIA. 4Electrical Department, Engineering Faculty, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Public Health and Community Medicine, Faculty of Medicine, Universitas Muhammadiyah Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Electronic Department, Engineering Faculty, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Institute of Ocean and Earth Sciences, Advanced Studies Complex, Universiti Malaya, 50603, Lembah Pantai, Kuala Lumpur, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Department of Radiology, Universitas Awalbros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Environmental and Policy Researcher, Environmental Science Program, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Muhamad Robiul Fuadi</style></author><author><style face="normal" font="default" size="100%">Jusak Nugraha</style></author><author><style face="normal" font="default" size="100%">I Gde Rurus Suryawan</style></author><author><style face="normal" font="default" size="100%">Hartono Kahar</style></author><author><style face="normal" font="default" size="100%">Aryati</style></author><author><style face="normal" font="default" size="100%">Gwenny Ichsan Prabowo</style></author><author><style face="normal" font="default" size="100%">Budi Utomo</style></author><author><style face="normal" font="default" size="100%">Reny I’tishom</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Correlation of Apo E Gene Polymorphism with Recurrent Acute Coronary Syndrome</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acute Coronary Syndrome</style></keyword><keyword><style  face="normal" font="default" size="100%">ApoE gene</style></keyword><keyword><style  face="normal" font="default" size="100%">PCR RFLP</style></keyword><keyword><style  face="normal" font="default" size="100%">Polymorphism</style></keyword><keyword><style  face="normal" font="default" size="100%">Public Health</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">450-453</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background&lt;/strong&gt;: Recurrent cardiovascular disease (CVD) incidence puts patients at higher risk for mortality and morbidity. One of the CVD symptoms is acute coronary syndrome (ACS). Many genetic polymorphisms are CVD risk factors. This study’s purpose was to investigate the correlation between recurrent ACS incidence and apolipoprotein E (ApoE) gene polymorphism.&lt;strong&gt; Method&lt;/strong&gt;: Case-control design was used in this study. About 90 patients who visited the cardiology and internal medicine clinics at UNAIR Hospital in Surabaya, Indonesia, served as the study's subjects. There were 30 patients with recurrent ACS, 30 patients with a single ACS, and 30 patients with no history of cardiovascular disease. Afterward, using the polymerase chain reaction-restriction fragment length method, the ApoE gene polymorphism examination was carried out. The Tropical Disease Center UNAIR Laboratory conducted all laboratory testing. R&lt;strong&gt;esults&lt;/strong&gt;: In the recurrent ACS group, ApoE polymorphism genotype patterns were 5 subjects for ε2ε2 (16.67%), 23 subjects for ε3ε3 (76.66%), and 2 subjects for ε4ε4 (6.67%). Meanwhile, in the single ACS group, ApoE polymorphism genotype patterns were 6 subjects for ε2ε2 (20%), 22 subjects for ε3ε3 (73.4%), 1 subject for ε4ε4 (3.33%), and 1 subject for ε2ε3 (3.33%). And, in the non- ACS group, ApoE polymorphism genotype patterns were4 subjects for ε2ε2 (13.34%), 25 subjects for ε3ε3 (83.33%), and1 subject for ε4ε4 (3.33%). There was no correlation of ApoE gene polymorphism with recurrent ACS incidence by Chi-square analysis (p &amp;gt; 0.05). &lt;strong&gt;Conclusion&lt;/strong&gt;: ApoE gene polymorphism cannot significantly affect recurrent ACS incidence.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">450</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Muhamad Robiul Fuadi&lt;sup&gt;1&lt;/sup&gt;, Jusak Nugraha&lt;sup&gt;2,*&lt;/sup&gt;, I Gde Rurus Suryawan&lt;sup&gt;3&lt;/sup&gt;, Hartono Kahar&lt;sup&gt;2&lt;/sup&gt;, Aryati&lt;sup&gt;2&lt;/sup&gt;, Gwenny Ichsan Prabowo&lt;sup&gt;4&lt;/sup&gt;, Budi Utomo&lt;sup&gt;5&lt;/sup&gt;, Reny I’tishom&lt;sup&gt;6&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctoral Program of Medical Science, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Clinical Pathology, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Cardiology and Vascular Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Physiology and Medical Biochemistry, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Public Health and Preventive Medicine Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Medical Biology, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Raden Muharam</style></author><author><style face="normal" font="default" size="100%">Nurhuda Sahar</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Luluk Yunaini</style></author><author><style face="normal" font="default" size="100%">Risqa Novita</style></author><author><style face="normal" font="default" size="100%">Rosalina Thuffi</style></author><author><style face="normal" font="default" size="100%">Conny Riana Tjampakasari</style></author><author><style face="normal" font="default" size="100%">Ponco Birowo</style></author><author><style face="normal" font="default" size="100%">Diyah Kristanty</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Decreased Expression of Endocrine Glands Vascular Endothelial Growth Factor (EG-VEGF) in Rat Endometrial After Stimulation with Recombinants FSH Can be Reduce Implantation Rates</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">EG-VEGF</style></keyword><keyword><style  face="normal" font="default" size="100%">Endometrial receptivity</style></keyword><keyword><style  face="normal" font="default" size="100%">rFSH</style></keyword><keyword><style  face="normal" font="default" size="100%">Secretory phase.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">707-713</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Decreased expression of EG-VEGF in human endometrium after administration of ovarian stimulators has been reported to adversely affect endometrial receptivity and low implantation rates. &lt;strong&gt;Objective:&lt;/strong&gt; To determine the effect of recombinant FSH administration on EG-VEGF protein in the endometrium of rats taken in the secretory phase and how it relates to endometrial receptivity. Design: A total of 36 female wistar rats with normal estrous cycles were randomly assigned to the natural cycle group (NC) and two stimulation groups (SC) which were injected with recombinant FSH at 12.5 IU and 25 IU intraperitoneally. Uterine necropsy and blood collection were performed on day 1, day 2, and day 3 after hCG administration. A total of 3 female rats from each group were mated with male rats (two males and three females in one cage). A successful marriage is indicated by the presence of a vaginal plug the next day. The level of EG-VEGF protein expression was assessed by immunohistochemical technique and steroid hormone levels were measured by the Elisa technique. &lt;strong&gt;Results&lt;/strong&gt;: ANOVA test, that the expression of EG-VEGF in the endometrial glands showed a significant decrease from the normal cycle group to the stimulated cycle group 1 (SC 1) and SC2 (P = 0.00), as well as the expression of EG-VEGF in the endometrial stroma. (P = 000). Steroid hormone levels did not show a significant decrease between the normal cycle group and the stimulated cycle group (P = 0.48 and P = 0.13). &lt;strong&gt;Conclusion:&lt;/strong&gt; Decreased EG-VEGF expression in rat endometrium after administration of recombinant FSH is associated with decreased endometrial receptivity which can reduce pregnancy rates.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">707</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Raden Muharam&lt;sup&gt;1&lt;/sup&gt;, Nurhuda Sahar&lt;sup&gt;2&lt;/sup&gt;, Kusmardi Kusmardi&lt;sup&gt;3,5,*&lt;/sup&gt;, Luluk Yunaini&lt;sup&gt;6&lt;/sup&gt;, Risqa Novita&lt;sup&gt;7&lt;/sup&gt;, Rosalina Thuffi&lt;sup&gt;8&lt;/sup&gt;, Conny Riana Tjampakasari&lt;sup&gt;9&lt;/sup&gt;, Ponco Birowo&lt;sup&gt;10&lt;/sup&gt;, Diyah Kristanty&lt;sup&gt;11&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Obstetrics and Gynecology, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pathology Anatomy, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Drug Development Research Center, Indonesia Medical Education and Research Institute, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Human Cancer Research Center, Indonesia Medical Education and Research Institute, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Center of Biomedical and Basic Health Technology, Ministry of Health of the Republic of Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Master Programe of Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Department of Microbiology, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Department of Urology Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Department of Clinical Pathology, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wachid Putranto</style></author><author><style face="normal" font="default" size="100%">Septina Hestiningrum</style></author><author><style face="normal" font="default" size="100%">Nur Ismi Mustika Febriani</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Ratih Tri Kusuma Dewi</style></author><author><style face="normal" font="default" size="100%">Santy Ayu Puspita Perdhana</style></author><author><style face="normal" font="default" size="100%">Nurhasan Agung Prabowo</style></author><author><style face="normal" font="default" size="100%">Yeremia Suryo Pratama</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Channa striata Extract on Serum Albumin and High Sensitive C-Reactive Protein in End-Stage Renal Disease Patients: A Randomized Controlled Trial</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Albumin</style></keyword><keyword><style  face="normal" font="default" size="100%">Channa striata</style></keyword><keyword><style  face="normal" font="default" size="100%">End-stage renal disease</style></keyword><keyword><style  face="normal" font="default" size="100%">hs-CRP</style></keyword><keyword><style  face="normal" font="default" size="100%">Supplementation.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">1-5</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Albumin is a marker of nutritioinal inflammation and mortality. Chronic inflammation, as indicated by the concentration of a proinflammatory cytokine, high sensitivity C-reactive protein (hs-CRP) was reported to be high in end-stage renal disease (ESRD) patients. &lt;em&gt;Channa striata&lt;/em&gt; (CS) contains high protein that can increase albumin levels and has anti-inflammatory effects. This study was conducted to determine the effect of CS extract on serum albumin and hs-CRP on ESRD patients. &lt;strong&gt;Methods: &lt;/strong&gt;This study is a randomized, double blind, placebo-controlled study in patients with ESRD on hemodialysis (HD) and continuous ambulatory peritoneal dialysis (CAPD). Subjects were randomized to either a CS or a placebo group and were given a three times daily dosage of 500 mg of CS extract or 500 mg maltodextrin, respectively for 21 days. Serum albumin and hs-CRP were measured at the baseline, and at the end of the study. &lt;strong&gt;Result: &lt;/strong&gt;Forty subjects were randomized into the study with 20 in the &lt;em&gt;Channa striata &lt;/em&gt;group and 20 in the placebo group, with HD and CAPD patient evenly distributed among the group. Significant increase in serum albumin levels (p&amp;lt;0,001) and significant decrease of hs-CRP (p&amp;lt;0,001) were observed in the treatment group compared to control group at the end of the study. At the end of the study, there was no significant difference between serum albumin, hs-CRP, and their gradient between HD and CAPD patients in the intervention group. &lt;strong&gt;Conclusion: &lt;/strong&gt;CS extract results in higher serum albumin and lower hs-CRP levels compared to placebo in our population.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">1</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Wachid Putranto&lt;sup&gt;1,2,*&lt;/sup&gt;, Septina Hestiningrum&lt;sup&gt;1,2&lt;/sup&gt;, Nur Ismi Mustika Febriani&lt;sup&gt;1,2&lt;/sup&gt;, Kusmardi Kusmardi&lt;sup&gt;3&lt;/sup&gt;, Ratih Tri Kusuma Dewi&lt;sup&gt;1,2&lt;/sup&gt;, Santy Ayu Puspita Perdhana&lt;sup&gt;1,2&lt;/sup&gt;, Nurhasan Agung Prabowo&lt;sup&gt;2,4&lt;/sup&gt;, Yeremia Suryo Pratama&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Nephrology, Department of Internal Medicine, Dr. Moewardi General Hospital, Faculty of Medicine, Sebelas Maret University, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Medicine, Sebelas Maret University, Surakarta, Jl. Ir. Sutami 36, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Anatomic Pathology, Doctoral Programme Study of Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Drug Development Research Cluster, Human Cancer Research Cluster, Indonesia Medical Educational and Research Institute, Jl. Salemba Raya No.6, Jakarta, 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Internal Medicine, Faculty of Medicine, Sebelas Maret University Hospital, Jl. A. Yani 200, Sukoharjo, INDONESIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Novi Primadewi</style></author><author><style face="normal" font="default" size="100%">Harijono Kariosentono</style></author><author><style face="normal" font="default" size="100%">Ari Probandari</style></author><author><style face="normal" font="default" size="100%">Budiyanti Wiboworini</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Combination between Green Tea Extract and Curcumin Extract from Mt. Lawu on BAX, Bcl-2 and Caspase-3 in Cisplatin-Induced Rat Models</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antiapoptotic</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Ototoxicity.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">370-374</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;The study determines effect of Combination between Green Tea and Curcumin Extract from Mount Lawu on BAX, Bcl-2 and Caspase-3 in Cisplatin (Cis)-induced rat models. &lt;strong&gt;Methods:&lt;/strong&gt; We treated four rats in each group and randomly distributed them into four groups: group C (−) was the negative control group with no treatment given, group C (+) was the positive control group given Cis only, group A1 was given green tea extract and curcumin extract combination after Cis, and group A2 was given Ginkgo biloba after Cis. Expression levels of BAX, Bcl-2, and Caspase-3 were assessed by ELISA. An ANOVA, a parametric test, was used if the data were normally distributed. If there were significant differences between the three groups regarding BAX, Bcl-2 and Caspase-3, a post hoc test was performed to determine the differences between treatments.&lt;strong&gt; Results:&lt;/strong&gt; The results of the study show that combination between green tea and curcumin extract can increase Bcl-2 levels with an average value of 15.42 + 0.76 ng/mL, better than Ginkgo biloba extract with a value of 13.50 + 0.47 ng/mL, reduce BAX and Caspase-3 levels with a value of 6.57 + 0.38 ng/mL and 2.89 + 0.19 ng/mL, better than Ginkgo biloba with a value of 7.34 + 1.06 ng/mL and 3.86 + 0.34 ng/mL. &lt;strong&gt;Conclusion: &lt;/strong&gt;This research shows that Combination between Green Tea and Curcumin Extract can increase Bcl-2 levels and reduce BAX and Caspase-3 in Cis rat models after fourteen days of treatment, better than Ginkgo biloba.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">370</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Novi Primadewi&lt;sup&gt;1,*&lt;/sup&gt;, Harijono Kariosentono&lt;sup&gt;2&lt;/sup&gt;, Ari Probandari&lt;sup&gt;3&lt;/sup&gt;, Budiyanti Wiboworini&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Medical Science Doctoral Study Program, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department Dermatovenereology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department Public Health, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Nutrition Sciences, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kadek Rachmawati</style></author><author><style face="normal" font="default" size="100%">Rochmah Kurnijasanti</style></author><author><style face="normal" font="default" size="100%">Emy Koestanti Sabdoningrum</style></author><author><style face="normal" font="default" size="100%">Sin War Naw</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effectiveness of Ketapang (Terminalia cattapa L.) Extract Against Avian Pathogenic Eschericia coli (APEC) Infections in Layer Performance</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Avian Pathogenic Escherichia coli.</style></keyword><keyword><style  face="normal" font="default" size="100%">Food security</style></keyword><keyword><style  face="normal" font="default" size="100%">Layer chicken performance</style></keyword><keyword><style  face="normal" font="default" size="100%">Terminalia cattapa L.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">417-422</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This study aimed to determine the activity of Ketapang extract (&lt;em&gt;Terminalia cattapa&lt;/em&gt; L.) in layers infected with APEC. In vitro study that was conducted dilution methods using Ketapang extract at 5%, 10%, 15%, 20%, 25% and 30% concentrations.&lt;em&gt; In vivo&lt;/em&gt; study was conducted by randomly dividing 20 layers into five treatment groups, four per group. The chickens (except in group P0−) were infected with APEC aged 24 weeks. Then, the treatment was conducted according to the divided groups in one week. The said treatments are P0− (uninfected APEC and unadministered with Ketapang extract), P0+ (infected with APEC and unadministered with Ketapang extract), and P1, P2, and P3 (infected with APEC and administered with Ketapang extract with 5%, 10%, and 20% concentrations, respectively). The data from layers’ performance were analyzed using ANOVA and Duncan’s test. The dilution method (MIC and MBC) exhibited the antibacterial ability of Ketapang extract against APEC at 5% dose. The Ketapang extract administration in layers exhibited improved performance of chickens infected with APEC, with the administration of 10% dose of Ketapang extract showing the best result. In summary, about 10% concentration Ketapang extract can serve as an antibacterial agent and showed the best results in layers infected with APEC.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">417</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kadek Rachmawati&lt;sup&gt;1,*&lt;/sup&gt;, Rochmah Kurnijasanti&lt;sup&gt;1&lt;/sup&gt;, Emy Koestanti Sabdoningrum&lt;sup&gt;2&lt;/sup&gt;, Sin War Naw&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Basic Veterinary Medicine Division, Faculty of Veterinary Medicine, Universitas Airlangga, 60115, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Animal Husbandry Division, Faculty of Veterinary Medicine, Universitas Airlangga, 60115, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Chemistry, Myitkyina University, Myitkyina, Myanmar&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sardar Hussain</style></author><author><style face="normal" font="default" size="100%">Komal KP</style></author><author><style face="normal" font="default" size="100%">Guruvayoorappan C</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Emilia Sonchifolia-A Critical and Comprehensive Review of its  Diverse Medicinal Potential and Future as Therapeutic</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-tumour</style></keyword><keyword><style  face="normal" font="default" size="100%">Emilia sonchifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal plant</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">1143-1149</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;em&gt;Emilia sonchifolia&lt;/em&gt; (L.) DC, it belongs to the family Asteraceae or Compositae, is conventionally used in ethnomedicine, and acquires various medicinal properties. This plant has been regarded as one of the widespread traditional vegetable salads in Malaysia, Bangladesh, and India. In addendum to its avail as a vegetable, the plant has been documented with several medicinal benefits in the extravagance of night blindness, epilepsy, malaria, asthma, burns, breast abscesses, and inflammatory diseases. On scrutinization of their pharmacological properties, it has been revealed that they possess numerous notable biological properties such as antimicrobial, analgesic, anti-inflammatory, antioxidant, hepatoprotective, antianxiety, and anticataract, as well as anticonvulsant activities. Concrete evidence suggests the presence of potential phytochemicals in this plant with a wide range of unknown applications. In this current review, we discuss the phytochemicals present in the plant &lt;em&gt;Emilia sonchifolia &lt;/em&gt;and emphasize the therapeutic and pharmacological activities reported so far concerning this plant.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1143</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Sardar Hussain&lt;sup&gt;1&lt;/sup&gt; , Komal KP&lt;sup&gt;2&lt;/sup&gt; , Guruvayoorappan C&lt;sup&gt;3&lt;/sup&gt;,*&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Ph.D. Scholar, R&amp;amp;D Centre, Bharathiar University, Coimbatore 641 046, Tamil Nādu; Assistant Professor, Department of Biotechnology, Government Science College, Chitradurga 577 501, Karnataka, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Assistant Professor, Department of Biochemistry, Government Science College, Chitradurga 577 501, Karnataka, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Associate Professor, Division of Cancer Research, Regional Cancer Centre, Thiruvananthapuram 695 011, Kerala, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sharada L. Deore</style></author><author><style face="normal" font="default" size="100%">Anjali A. Kide</style></author><author><style face="normal" font="default" size="100%">Bhushan A. Baviskar</style></author><author><style face="normal" font="default" size="100%">Somshekhar S. Khadabadi</style></author><author><style face="normal" font="default" size="100%">Bhavana A Shende</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Neuroprotective Efficacy of Indian Shankhpushpi Varieties in Alzheimer’s disease – North Vs South</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alzheimer’s disease</style></keyword><keyword><style  face="normal" font="default" size="100%">Dementia</style></keyword><keyword><style  face="normal" font="default" size="100%">Scopolamine</style></keyword><keyword><style  face="normal" font="default" size="100%">Scopoletin.</style></keyword><keyword><style  face="normal" font="default" size="100%">taraxerol</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">372-377</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background&lt;/strong&gt;: Shankhpushpi is a well-known Ayurvedic memory enhancing medicine associated with controversy. Among the various varieties, Convolvulus pleuricaulis and Clitorea ternatia are widely used in commercial memory enhancing formulations under the name of Shankhpushpi. Convolvulus pleuricaulis is recognized as true shankhpushpi in North side of India, however in southern part of India, Clitorea ternatia is accepted as Shankhpushpi. &lt;strong&gt;Objectives:&lt;/strong&gt; The present study aims to compare neuroprotective efficacy of &lt;em&gt;C. pleuricaulis &lt;/em&gt;and &lt;em&gt;C. ternatea&lt;/em&gt; by &lt;em&gt;in vitro&lt;/em&gt;, &lt;em&gt;in vivo &lt;/em&gt;methods and establish scientifically validated data to choose appropriate shankhpushpi variety for commercial use. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Both herbs were extracted in the Soxhlet apparatus with 70% ethanol for 5 - 6 hours at 60 - 65̊ C. The presence of neuroprotective principles - taraxerol and scopoletin in extracts was confirmed by the Thin Layer Chromatography. The preliminary screening for neuroprotective efficacy of extracts was done by in vitro free radical scavenging, Acetyl cholinesterase enzyme inhibition and LOX enzyme level estimation. Invivo study of extracts included behavioral assessment of adult rats by Y maze, Morris water maze using scopolamine induced Alzheimer’s disease like model. &lt;strong&gt;Result: &lt;/strong&gt;Extracts of both &lt;em&gt;C. pleuricaulis&lt;/em&gt; and &lt;em&gt;C. ternatea &lt;/em&gt;significantly scavenged free radicals, inhibited acetyl cholinesterase and LOX enzyme in vitro. But in in-vivo study, significant retention of spatial and working memory was observed in rats administered with &lt;em&gt;C. pleuricaulis&lt;/em&gt; as compared to&lt;em&gt; C. ternatea.&lt;/em&gt; &lt;strong&gt;Conclusion: &lt;/strong&gt;&lt;em&gt;C. pleuricaulis &lt;/em&gt;more significantly shields against memory loss and dementia by reducing oxidative stress, inflammation, and memory impairment. Hence should be used in commericial neuroprotective formulation as chief source of Shankhpushpi instead of &lt;em&gt;C. ternatea.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">372</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Sharada L. Deore, Anjali A. Kide*, Bhushan A. Baviskar, Somshekhar S. Khadabadi, Bhavana A Shende&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Government College of Pharmacy, Kathora Naka, Amravati -444601, Maharshtra, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Daya Banyu Bening</style></author><author><style face="normal" font="default" size="100%">Reni Prastyani</style></author><author><style face="normal" font="default" size="100%">Nurwasis</style></author><author><style face="normal" font="default" size="100%">Evelyn Komaratih</style></author><author><style face="normal" font="default" size="100%">Ismi Zuhria</style></author><author><style face="normal" font="default" size="100%">Hari Basuki Notobroto</style></author><author><style face="normal" font="default" size="100%">Dyah Fauziah</style></author><author><style face="normal" font="default" size="100%">Chrismawan Ardianto</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Expressions of Matrix Metalloproteinase-3 and Tissue Inhibitor Metalloproteinase-1 in Corneal Tissue Post Alkali Burn Treated with Topical Medroxyprogesterone Acetate and Doxycycline</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Corneal alkali burn</style></keyword><keyword><style  face="normal" font="default" size="100%">Doxycycline.</style></keyword><keyword><style  face="normal" font="default" size="100%">Medroxyprogesterone acetate</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">553-557</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Purpose: &lt;/strong&gt;This study aims to investigate the effects of topical Medroxyprogesterone acetate (MPA) and Doxycycline in inhibiting the expression of MMP-3 and TIMP-1 in ocular alkali burn models in animals. &lt;strong&gt;Methods: &lt;/strong&gt;A total of 18 New Zealand Rabbits were divided into 3 groups based on their post-alkali-burn treatment: PBS (G1/ control group), topical Doxycycline 1mg/ml (G2), and topical MPA 1% (G3). Alkali burn models were made by exposing 1N NaOH solution to the central cornea for 30 seconds. MMP-3 and TIMP-1 expression were evaluated using immunohistochemistry after 14 days of treatment. &lt;strong&gt;Results:&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;Statistically significant differences in the mean MMP-3 expression were found between the three groups (p=0.010). There was a significant difference in MMP-3 expression between the control group with MPA (p=0.017) and Doxycycline (p=0.028) but was not found between the MPA and Doxycycline groups (p=1,000). The mean differences in TIMP-1 expression between the three treatment groups were statistically significant (p=0.005), with a significant difference between the control group with Doxycycline (p=0.022) and MPA (p=0.007). There was no significant difference in TIMP-1 expression between the Doxycycline and MPA groups (P=1,000). &lt;strong&gt;Conclusion: &lt;/strong&gt;This study indicated that topical administration of Doxycycline or MPA in ocular alkali burn reduces the expression of MMP-3 and TIMP-1.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">553</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Daya Banyu Bening&lt;sup&gt;1&lt;/sup&gt;, Reni Prastyani&lt;sup&gt;1,*&lt;/sup&gt;, Nurwasis&lt;sup&gt;1&lt;/sup&gt;, Evelyn Komaratih&lt;sup&gt;1&lt;/sup&gt;, Ismi Zuhria&lt;sup&gt;1&lt;/sup&gt;, Hari Basuki Notobroto&lt;sup&gt;2&lt;/sup&gt;, Dyah Fauziah&lt;sup&gt;3&lt;/sup&gt;, Chrismawan Ardianto&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Ophthalmology, Dr. Soetomo General Academic Hospital / Faculty of Medicine, Airlangga University, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biostatistics and Population, Faculty of Public Health, Airlangga University, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Anatomical Pathology, Faculty of Medicine, Airlangga University, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Clinical Pharmacy, Faculty of Pharmacy, Airlangga University, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sunadi</style></author><author><style face="normal" font="default" size="100%">Saddam Al Aziz</style></author><author><style face="normal" font="default" size="100%">Fadhilah Fitri</style></author><author><style face="normal" font="default" size="100%">Devni Prima Sari</style></author><author><style face="normal" font="default" size="100%">Muhammad Raffi Ghifari</style></author><author><style face="normal" font="default" size="100%">Rismi Verawati</style></author><author><style face="normal" font="default" size="100%">Nita Yessirita</style></author><author><style face="normal" font="default" size="100%">Oski Illiandri</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Putri Azhari</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hepatitis E Inhibited by Rosmarinic Acid Extract from Clove Plant (Syzygium Aromaricum) through Computational Analysis</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hepatitis E</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular Docking.</style></keyword><keyword><style  face="normal" font="default" size="100%">Rosmarinic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Syzygium aromaricum</style></keyword><keyword><style  face="normal" font="default" size="100%">Tyrosine FYN</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">518-523</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This study aims to evaluate the potential of Rosmarinic Acid as an inhibitor against Hepatitis E by interacting with the active site of the Tyrosine FYN protein. Computational approaches were employed to predict the molecular interactions between Rosmarinic Acid and Tyrosine FYN. The research methodology involved the use of software such as Pymol, Pyrex, Protein Plus, and the Lepinski Rule. Docking analysis was conducted using Pymol to obtain information about the binding energy between Rosmarinic Acid and Tyrosine FYN. The results of the analysis showed that Rosmarinic Acid exhibited a Binding Affinity of -8.3, -8, and -7.9, indicating a strong affinity towards the target protein. Additionally, Root Mean Square Deviation (RMSD) values of 0, 15.905, and 17.014 were used to assess the stability of the formed protein-ligand complex. Analysis using Protein Plus revealed interactions between Rosmarinic Acid and Tyrosine FYN. Furthermore, analysis using the Lepinski Rule to examine the physicochemical properties of Rosmarinic Acid indicated that the molecule had a mass of 360, 5 hydrogen bond donors, 8 hydrogen bond acceptors, a log P value of 1.76, and a molar reactivity of 89.8. These findings highlight the potential of Rosmarinic Acid as an inhibitor of Hepatitis E through its interaction with the Tyrosine FYN protein, providing a basis for the development of potential new therapies in the treatment of this disease.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">518</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sunadi1, Saddam Al Aziz&lt;sup&gt;2&lt;/sup&gt;, Fadhilah Fitri&lt;sup&gt;3&lt;/sup&gt;, Devni Prima Sari&lt;sup&gt;4&lt;/sup&gt;, Muhammad Raffi Ghifari&lt;sup&gt;5&lt;/sup&gt;, Rismi Verawati&lt;sup&gt;6&lt;/sup&gt;, Nita&amp;nbsp;Yessirita&lt;sup&gt;7&lt;/sup&gt;, Oski Illiandri&lt;sup&gt;8&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;9&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;10&lt;/sup&gt;, Putri Azhari&lt;sup&gt;11&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;6,12,*&lt;/sup&gt;, Viol&amp;nbsp;Dhea Kharisma&lt;sup&gt;13,14&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;15&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;16,17&lt;/sup&gt;, ANM Ansori&lt;sup&gt;13,15&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Agrotechnology Study Program, Faculty of Agriculture, Universitas Tamansiswa, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Mathematics Department, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Statistics Department, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Mathematics Department, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Agricultural Product Technology Study Program, Faculty of Agriculture, Universitas Ekasakti, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Department of Biomedicine, Faculty of Medicine, Universitas Lambung Mangkurat, Banjarmasin, South Kalimantan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Environmental and Policy Researcher, Environmental Science Program, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Department of Radiology, Universitas Awalbros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Department of Agricultural Technology, Faculty of Agricultural Technology, Universitas Andalas, Padang, West Sumatra, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;16&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;17&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nita Yessirita</style></author><author><style face="normal" font="default" size="100%">Rismi Verawati</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Rollando Rollando</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Muhammad Thoriq Albari</style></author><author><style face="normal" font="default" size="100%">Putri Azhari</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Silico Study of Rhamnocitrin Extract from Clove Syzygium Aromaricum in Inhibiting Adenosine A1 Adenylate Cyclase Interaction</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adenosine A1</style></keyword><keyword><style  face="normal" font="default" size="100%">Adenylate Cyclase inhibition</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular Docking.</style></keyword><keyword><style  face="normal" font="default" size="100%">Rhamnocitrin</style></keyword><keyword><style  face="normal" font="default" size="100%">Syzygium aromaricum</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">512-517</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This study aims to analyze the potential of Rhamnocitrin, a compound found in clove extract (Syzygium aromaticum), as an inhibitor of Adenylate Cyclase through an in-silico approach. The research method involves the use of software such as Pymol, PyRx, Protein Plus, and Lipinski Rule for molecular interaction analysis and physicochemical characterization of Rhamnocitrin. The analysis results show that Rhamnocitrin has significant affinity towards Adenosine A1 with Binding Affinity values of -6.1, -5.8, and -5.7. RMSD analysis indicates good stability of the formed protein-ligand complexes, with RMSD values of 0, 3.129, and 3.696. Analysis using Protein Plus software reveals the interaction between Rhamnocitrin and Adenosine A1, while the lipinski analysis shows physicochemical characteristics of Rhamnocitrin that meet important criteria, such as a mass of 300, 3 hydrogen bond donors, 6 hydrogen bond acceptors, log P of 2.6, and molar reactivity of 77.27. These findings provide new insights into the development of potential therapies involving clove extract and Rhamnocitrin as inhibitors of Adenylate Cyclase, and further research is needed to validate their effectiveness and safety.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">512</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nita Yessirita&lt;sup&gt;1&lt;/sup&gt;, Rismi Verawati&lt;sup&gt;2&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;3&lt;/sup&gt;, Rollando Rollando&lt;sup&gt;4&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;5&lt;/sup&gt;, Muhammad Thoriq Albari&lt;sup&gt;6&lt;/sup&gt;, Putri Azhari&lt;sup&gt;7&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;2,8,*&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;9,10&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;11&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;12,13&lt;/sup&gt;, ANM Ansori&lt;sup&gt;9,10,11&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Agricultural Product Technology Study Program, Faculty of Agriculture, Universitas Ekasakti, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Radiology, Universitas Awalbros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Program of Pharmacy, Faculty of Science and Technology, Universitas Ma Chung, Malang 65151, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Environmental and Policy Researcher, Environmental Science Program, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Agricultural Technology, Faculty of Agricultural Technology, Universitas Andalas, Padang, West Sumatra, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Generasi Biologi Indonesia Foundation, Gresik, INDONESIA. 11Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Linda Rosalina</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Rismi Verawati</style></author><author><style face="normal" font="default" size="100%">Okta Suryani</style></author><author><style face="normal" font="default" size="100%">Muhammad Arya Ghifari</style></author><author><style face="normal" font="default" size="100%">Amalia Putri Lubis</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Silico Study on the Inhibition of Sitogluside from Clove Plant (Syzygium aromaticum) on Interleukin 2 in B and T Cell Proliferation</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cell Proliferation</style></keyword><keyword><style  face="normal" font="default" size="100%">Interleukin-2</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword><keyword><style  face="normal" font="default" size="100%">Sitogluside</style></keyword><keyword><style  face="normal" font="default" size="100%">Syzygium.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">575-580</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This research discusses an in-silico study of sitogluside found in the clove plant (&lt;em&gt;Syzygium aromaticum&lt;/em&gt;) as a potential inhibitor of B and T cell proliferation through interaction with Interleukin-2. This study utilizes methods such as Swiss Target Prediction, Pymol, Pyrex, Protein Plus, and Lipinski's Rule to predict the biological activity and pharmacokinetic characteristics of sitogluside. From the docking simulation results, sitogluside exhibited strong interactions with interleukin-2 with RMSD values of 0, 1.637, and 2.299, and Binding Affinities of -5.7, -5.5, and -5.5, indicating its potential effectiveness as an inhibitor. In addition, sitogluside fulfills Lipinski's rule with a molecular mass of 520, 4 hydrogen bond donors and acceptors, a log P value of 2.3, and a molar reactivity of 133, indicating a high potential for good bioavailability in biological systems. These results suggest that sitogluside from the clove plant holds potential as a new therapy in inhibiting B and T cell proliferation, however further research is needed to validate these findings and explore its potential in clinical treatments.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">575</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Linda Rosalina&lt;sup&gt;1&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;2&lt;/sup&gt;, Rismi Verawati&lt;sup&gt;3&lt;/sup&gt;, Okta Suryani&lt;sup&gt;3&lt;/sup&gt;, Muhammad Arya Ghifari&lt;sup&gt;4&lt;/sup&gt;, Amalia Putri Lubis&lt;sup&gt;3&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;3&lt;/sup&gt;,*, Riso Sari Mandeli&lt;sup&gt;5&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;6,7&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;8&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;9,10&lt;/sup&gt;, ANM Ansori&lt;sup&gt;6,7,8&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Makeup and Beauty, Faculty of Tourism and Hospitality, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Radiology Engineering, Universitas Awalbros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Environmental and Policy Researcher, Environmental Science Program, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA. 7Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Rismi Verawati</style></author><author><style face="normal" font="default" size="100%">Agus Suprijono</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Asri Peni Wulandari</style></author><author><style face="normal" font="default" size="100%">Dony Novaliendry</style></author><author><style face="normal" font="default" size="100%">Ritmaleni</style></author><author><style face="normal" font="default" size="100%">Linda Rosalina</style></author><author><style face="normal" font="default" size="100%">Muhammad Arya Ghifari</style></author><author><style face="normal" font="default" size="100%">Amalia Putri Lubis</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Silico Study on the Potential of Guaiacol Extract from Green Tea (Camellia sinensis) as a Stimulant for Carbanoic Anhydrase II in Renal Tubular Acidosis</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Camellia sinensis.</style></keyword><keyword><style  face="normal" font="default" size="100%">Carbanoic Anhydrase II</style></keyword><keyword><style  face="normal" font="default" size="100%">Guaiacol</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword><keyword><style  face="normal" font="default" size="100%">Renal Tubular Acidosis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">494-499</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This study explores the potential of Guaiacol, a green tea extract from &lt;em&gt;Camellia &lt;/em&gt;sinensis, as a stimulant in renal tubular acidosis through &lt;em&gt;in-silico&lt;/em&gt; investigation on the Carbanoic Anhydrase II enzyme. Utilizing comprehensive computational tools including PyMOL, PyRx, Protein Plus, and the Lipinski's Rule of Five, a detailed examination of the molecular structure and its interactions with the target enzyme was conducted. The results from Protein Plus revealed interactions between Guaiacol and Carbanoic Anhydrase II. Quantitative parameters were determined with Binding Affinity values of -5, -4.7, and -4.5, along with RMSD values of 0, 0.956, and 1.412. The Lipinski's Rule of Five was employed to evaluate the compound's drug-like properties, with the findings indicating a molecular weight of 124, one hydrogen bond donor, two hydrogen bond acceptors, a log P of 1.4, and a molar reactivity of 34.65. Overall, these findings suggest that Guaiacol holds promising therapeutic potential in the treatment of renal tubular acidosis.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">494</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Rahadian Zainul&lt;sup&gt;1,9,*&lt;/sup&gt;, Rismi Verawati&lt;sup&gt;1&lt;/sup&gt;, Agus Suprijono&lt;sup&gt;2&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;3&lt;/sup&gt;, Asri Peni Wulandari&lt;sup&gt;4&lt;/sup&gt;, Dony Novaliendry&lt;sup&gt;5&lt;/sup&gt;, Ritmaleni6, Linda Rosalina&lt;sup&gt;7&lt;/sup&gt;, Muhammad Arya Ghifari&lt;sup&gt;8&lt;/sup&gt;, Amalia Putri Lubis&lt;sup&gt;1&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;10,11&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;12&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;13,14&lt;/sup&gt;, ANM Ansori&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;10,12&lt;/strong&gt; &lt;/sup&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacy, Sekolah Tinggi Ilmu Farmasi Yayasan Pharmasi Semarang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Environmental and Policy Researcher, Environmental Science Program Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Electronic Department, Engineering Faculty, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Laboratory of Medicinal Chemistry, Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Universitas Gadjah Mada, North Sekip, Yogyakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Makeup and Beauty, Faculty of Tourism and Hospitality, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wirda Anggraini</style></author><author><style face="normal" font="default" size="100%">Djoko Agus Purwanto</style></author><author><style face="normal" font="default" size="100%">Idha Kusumawati</style></author><author><style face="normal" font="default" size="100%">Isnaeni3, Suryanto</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of the Environment on Biofilm Formation Candida albicans of Vulvovaginal Candidiasis Isolate Patient</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biofilm formation; Candida albicans; sabourau dextrose broth; potato dextrose broth; vulvovaginal candidiasis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">216-222</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Context: &lt;/strong&gt;Candida albicans is a type of fungus that can produce biofilms and may cause Vulvovaginal Candidiasis (VVC) disease. We investigated the effect of environment on biofilm formation of &lt;em&gt;C. albicans&lt;/em&gt; patient isolates and ATCC 14053. Biofilm formation is influenced by several factors such as environments and nutrients. Objectives: To investigated the effect of environment on biofilm formation of &lt;em&gt;C. albicans&lt;/em&gt; patient isolates and ATCC 14053. &lt;strong&gt;Methods:&lt;/strong&gt; The samples using &lt;em&gt;C. albican&lt;/em&gt;s ATCC 14053,&lt;em&gt; C. albicans,&lt;/em&gt; which may form biofilms, was isolated from patient Dermatology and Venereology and Obstetrics and Gynecology from a hospital in Malang. TCP (A tissue Culture Plate) is the biofilm formation method used. &lt;strong&gt;Results: &lt;/strong&gt;Biofilm formation took 48-72 hours at 25 °C and 96-120 hours at 37 °C. Based on the result biofilm formation of &lt;em&gt;C. albicans&lt;/em&gt; is influenced by environmental factors and characterized by a high OD value. &lt;strong&gt;Conclusions:&lt;/strong&gt; Biofilm formation is accelerated in temperature incubation needed at 25 °C for 48-72 hours, using biomass 107 CFU/mL, nutrition using Potato Dextrose Broth media and 1% glucose, and the solvent of 30% acetic acid to obtain acid condition.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">216</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Wirda Anggraini&lt;sup&gt;1,2&lt;/sup&gt;, Djoko Agus Purwanto&lt;sup&gt;1*&lt;/sup&gt;, Idha Kusumawati&lt;sup&gt;1&lt;/sup&gt;, Isnaeni&lt;sup&gt;3&lt;/sup&gt;, Suryanto&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctor of Science Pharmacy, Faculty Pharmacy, Airlangga University, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacy, Faculty Medicine and Health Sciences, Maulana Malik Ibrahim State Islamic University Malang, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacy, Faculty Health Science, Muhammadiyah University Surabaya, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Master Student of Science Pharmacy, Faculty of Pharmacy, Airlangga University, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Rismi Verawati</style></author><author><style face="normal" font="default" size="100%">Gemini Alam</style></author><author><style face="normal" font="default" size="100%">Khoirun Nisyak</style></author><author><style face="normal" font="default" size="100%">Trisna Kumala Sari</style></author><author><style face="normal" font="default" size="100%">Muhammad Arya Ghifari</style></author><author><style face="normal" font="default" size="100%">Ritbey Ruga</style></author><author><style face="normal" font="default" size="100%">Putri Azhari</style></author><author><style face="normal" font="default" size="100%">Romadhon</style></author><author><style face="normal" font="default" size="100%">Himmatul Barroroh</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Interaction of Cynaroside from Orthosiphon Aristatus Plant Extract on TNF Alpha as a Stimulant in Malaria and Asthma</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Asthma.</style></keyword><keyword><style  face="normal" font="default" size="100%">Cynaroside</style></keyword><keyword><style  face="normal" font="default" size="100%">Malaria</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword><keyword><style  face="normal" font="default" size="100%">Orthosiphon aristatus</style></keyword><keyword><style  face="normal" font="default" size="100%">TNF Alpha</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">581-586</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This research aims to investigate the interaction between cynaroside, a natural compound found in &lt;em&gt;Orthosiphon aristatus&lt;/em&gt; plant extract, with TNF Alpha as a stimulant in the context of malaria and asthma. The research method involved an&lt;em&gt; in-silico &lt;/em&gt;approach using software such as Pymol, PyRx, Protein Plus, and the Lepinski Rule. The results of the study showed that cynaroside has a significant interaction with TNF Alpha, as indicated by high Binding Affinity values of -9.6, -9.3, and -9.2. Analysis using Protein Plus confirmed the interaction between cynaroside and TNF Alpha. Additionally, evaluation using the Lepinski Rule of Five revealed that cynaroside has physicochemical characteristics suitable as a potential drug compound, with a mass of 448, hydrogen bond donors of 7, hydrogen bond acceptors of 11, log p -0.401, and molar reactivity of 105.2. These findings provide a deeper understanding of the potential of cynaroside in regulating the immune response to malaria and asthma through its interaction with TNF Alpha. These results can serve as an important basis for further research in the development of more targeted and effective therapies for both of these diseases&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">581</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Rahadian Zainul&lt;sup&gt;1,11,*&lt;/sup&gt;, Rismi Verawati&lt;sup&gt;1&lt;/sup&gt;, Gemini Alam&lt;sup&gt;2&lt;/sup&gt;, Khoirun Nisyak&lt;sup&gt;3&lt;/sup&gt;, Trisna Kumala Sari&lt;sup&gt;1&lt;/sup&gt;, Muhammad Arya Ghifari&lt;sup&gt;4&lt;/sup&gt;, Ritbey Ruga&lt;sup&gt;5&lt;/sup&gt;, Putri Azhari&lt;sup&gt;6&lt;/sup&gt;, Romadhon&lt;sup&gt;7&lt;/sup&gt;, Himmatul Barroroh&lt;sup&gt;8&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;9&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;10&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;12,13&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;14&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;15,16&lt;/sup&gt;, ANM Ansori&lt;sup&gt;12,13,14&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacognosy-Phytochemistry Laboratory, Faculty of Pharmacy, Universitas Hasanuddin, Makassar, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacy, Faculty of Health Science, Universitas Anwar Medika, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Mulawarman, Samarinda, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Agricultural Technology, Faculty of Agricultural Technology, Universitas Andalas, Padang, West Sumatra, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Fisheries Product Technology Study Program, Universitas Diponegoro Semarang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Chemistry Department, Faculty of Science and Technology, Universitas Islam Maulana Malik Ibrahim, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Environmental and Policy Researcher, Environmental Science Program, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Department of Radiology, Universitas Awalbros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;16&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fatmawati</style></author><author><style face="normal" font="default" size="100%">Suriana Koro</style></author><author><style face="normal" font="default" size="100%">Nadimin</style></author><author><style face="normal" font="default" size="100%">Kameriah Gani</style></author><author><style face="normal" font="default" size="100%">Hasan</style></author><author><style face="normal" font="default" size="100%">Ellyani Abadi</style></author><author><style face="normal" font="default" size="100%">Anwar Mallongi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Intervention of Giving Moringa Biscuits (Moringa Oliefera) Mix Sori Fish Flour to Increased Blood Hemoglobin Levels in Young Girls, Kendari, INDONESIA</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adolescents.</style></keyword><keyword><style  face="normal" font="default" size="100%">Blood Haemoglobin</style></keyword><keyword><style  face="normal" font="default" size="100%">Moringa Biscuits</style></keyword><keyword><style  face="normal" font="default" size="100%">Sori Fish</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">414-417</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Adolescents are the next generation and national development assets, one of the nutritional problems in adolescents is anemia, namely the lack of hemoglobin levels below normal (12 mg/dl). Efforts to deal with anemia are making food in the form of Moringa biscuits and sori fish which are rich in nutrients. The purpose of this study was to determine the effect of giving Moringa mixed sori biscuits on blood hemoglobin levels in adolescents. The type of research is a quasi-experimental conducted in June- September 2021 at Coastal Region Public Middle Schools throughout Kendari City in 2021, namely at SMPN 4 Kendari, SMPN 5 Kendari, SMPN 10 Kendari, SMPN 15 Kendari and SMPN 16 Kendari. The sample is anemic adolescent girls in the coastal area of Kendari City. The intervention sample was anemic adolescent girls who were given moringa biscuits mixed with sori fish flour as many as 36 people and the control sample was anemic adolescent girls who were not given moringa biscuits mixed with sori fish flour as many as 36 people. The case sampling technique used cluster random sampling and the control sample used matching. Data collection of blood hemoglobin levels using a portable device brand Easy Touch Meter. Data were analyzed using independent t-test test. The results of the study found blood hemoglobin levels before and after Moringa biscuits were given, namely in the case group before the intervention the average Hb level reached 10.51 mg/dl and after the intervention it reached 12.45 mg/ dl, while in the control group before the intervention it was 12.79 mg/dl and after intervention 13.49 mg/ dl. The results of the independent t-test obtained p value 0.000. The conclusion is that there is an effect of giving Moringa fish biscuits mixed with Sori fish flour on hemoglobin levels. Suggestions for young women are expected to increase the intake of protein sources of nutrients such as fish, eggs, tofu and tempeh and iron (Fe) which can be obtained from green vegetables such as Moringa to prevent and treat anemia.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">414</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Fatmawati&lt;sup&gt;1&lt;/sup&gt;, Suriana Koro&lt;sup&gt;2&lt;/sup&gt;, Nadimin&lt;sup&gt;3&lt;/sup&gt;, Kameriah Gani&lt;sup&gt;4&lt;/sup&gt;, Hasan&lt;sup&gt;5&lt;/sup&gt;, Ellyani Abadi&lt;sup&gt;6&lt;/sup&gt;, Anwar Mallongi&lt;sup&gt;7,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Nutrition, Polytechnic of the Ministry of Health, Kendari, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Nutrition, Polytechnic of the Ministry of Health, Kendari, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Public Health, Hasanuddin University Makassar, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Nutrition, Polytechnic of the Ministry of Health, Kendari, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Nutrition, Polytechnic of the Ministry of Health, Kendari, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Undergraduate Nutrition Study Program, STIKes Karya Kesehatan, Kendari, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Environmental Health, Faculty of Public Health, Hasanuddin University, Makassar, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amelia Shinta Prasetya</style></author><author><style face="normal" font="default" size="100%">Evelyn Komaratih</style></author><author><style face="normal" font="default" size="100%">Wimbo Sasono</style></author><author><style face="normal" font="default" size="100%">Mercia Chrysanti</style></author><author><style face="normal" font="default" size="100%">Maria Debora Niken Larasati</style></author><author><style face="normal" font="default" size="100%">I Ketut Sudiana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Intravitreal Resveratrol as Anti Apoptotic Agent Against Retinal  Ganglion Cell Loss in Ischemic Reperfusion Injury</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Apoptosis</style></keyword><keyword><style  face="normal" font="default" size="100%">Glaucoma</style></keyword><keyword><style  face="normal" font="default" size="100%">Ischemic-reperfusion injury</style></keyword><keyword><style  face="normal" font="default" size="100%">Neuroprotective</style></keyword><keyword><style  face="normal" font="default" size="100%">Resveratrol</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">1207-1212</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Glaucoma is an optic neuropathy caused by the apoptosis of retinal ganglion cells and results in progressive retinal ganglion cell injury. A decrease in intraocular pressure (IOP) is a modifiable risk factor for slowing the progression of the disease, and can be accomplished through medication, laser therapy, or surgery. Even though the intraocular pressure has decreased and attained normal levels, the injury to the retinal ganglion cells continues in some cases. It is believed that neuroprotective administration has a positive effect on preventing the loss of retinal ganglion cells.&lt;strong&gt; Methods:&lt;/strong&gt; Bax and Caspase-3 expression were measured involving 20 eyeballs of Rattus Norvegicus by immunohistochemistry examination. I-R injury was developed by increasing intraocular pressure (IOP) through the intracameral balanced salt solution (BSS) injection, then lowered after 60 minutes. Samples were divided into 4 groups: control, no further injection group, phosphate-buffered saline (PBS)-injected group and resveratrol-injected group. Each group was enucleated at days 7, 0, 7, and 7, respectively. Data with a non-normal distribution were examined using the Kruskal-Wallis test, and if the outcome was significant, the Mann-Whitney test. &lt;strong&gt;Results:&lt;/strong&gt; The highest mean Bax and Caspase-3 expression was found in PBS injected and enucleated at day 7 group (G2), 0.96±0.40 and 0.72 ± 0.30, respectively. When compared to PBS injection, the expression of Bax and Caspase-3 was lower in the resveratrol-injected group. &lt;strong&gt;Conclusion: &lt;/strong&gt;Bax and Caspase-3 expressions were lower in the intravitreal injection of Resveratrol in the dose of 100 µM following the I-R injury group compared to the group without intravitreal Resveratrol injection.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1207</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Amelia Shinta Prasetya&lt;sup&gt;1&lt;/sup&gt; , Evelyn Komaratih&lt;sup&gt;1,*&lt;/sup&gt;, Wimbo Sasono&lt;sup&gt;1&lt;/sup&gt; , Mercia Chrysanti&lt;sup&gt;1&lt;/sup&gt; , Maria Debora Niken Larasati&lt;sup&gt;1&lt;/sup&gt; , I Ketut Sudiana&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Ophthalmology, Faculty of Medicine, Universitas Airlangga/Dr. Soetomo General Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Departement of Anatomical Pathology, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sucharat Tungsukruthai</style></author><author><style face="normal" font="default" size="100%">Runtikan Pochairach</style></author><author><style face="normal" font="default" size="100%">Aungkana Krajarng</style></author><author><style face="normal" font="default" size="100%">Piracha Jumpa-ngern</style></author><author><style face="normal" font="default" size="100%">Parunkul Tungsukruthai</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Investigation of The Network Pharmacology and Mechanism of Action of Centella Asiatica Extract on The Atopic Dermatitis Model</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Atopic dermatitis</style></keyword><keyword><style  face="normal" font="default" size="100%">Centella asiatica</style></keyword><keyword><style  face="normal" font="default" size="100%">Network pharmacology</style></keyword><keyword><style  face="normal" font="default" size="100%">Skin inflammation.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">881-890</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Atopic dermatitis (AD) is a chronic relapsing inflammatory skin condition which has a negative impact on children health. The well-known medicinal plant Centella asiatica extract (CE) is used in herbal skin care products to produce various pharmacological effects in dermatology. However, the molecular target of CE in suppressing inflammatory is largely unknown. &lt;strong&gt;Objective&lt;/strong&gt;: the aim of this study was to examine anti-inflammatory properties and network pharmacology of CE in lipopolysaccharide (LPS)- induced AD &lt;em&gt;in vitro&lt;/em&gt; model.&lt;strong&gt; Method:&lt;/strong&gt; RAW264.7 cells were pre-treated with CE and then were stimulated with LPS and then were investigated cell viability, NO production, and the levels of pro-inflammatory mediators. In addition, the Search Tool for Retrieval of Interacting Genes (STRING), SwissTargetPrediction and the Kyoto Encyclopedia of Genes and Genomes (KEGG) were used to construct the defined mechanism of action and network pharmacology. &lt;strong&gt;Results:&lt;/strong&gt; CE showed the potent inhibitory effects on LPS-induced NO. In addition, CE significantly suppressed the expression of iNOS and COX-2, as well as the production of IL-2, IL-6, IL-10, and TNF- α. Furthermore, the network pharmacological analysis revealed the potential role of CE in biological processes such as regulating JAK/STATs pathway and inhibiting proinflammatory cytokines both of which were linked to AD pathogenesis. &lt;strong&gt;Conclusion:&lt;/strong&gt; Our findings confirm our hypothesis that CE could be developed as a therapeutic therapy for atopic dermatitis due to its pharmacological action and signaling mechanism in the modulation of allergic skin inflammation.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">881</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sucharat Tungsukruthai&lt;sup&gt;1&lt;/sup&gt;, Runtikan Pochairach&lt;sup&gt;2&lt;/sup&gt;, Aungkana Krajarng&lt;sup&gt;3&lt;/sup&gt;, Piracha Jumpa-ngern&lt;sup&gt;3&lt;/sup&gt;, Parunkul Tungsukruthai&lt;sup&gt;3,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Health and Applied Sciences, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90110, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Thammasat University Research Unit in Mechanisms of Drug Action and Molecular Imaging, Drug Discovery and Development Center, Office of Advanced Science and Technology, Thammasat University, Pathum Thani 12120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Chulabhorn International College of Medicine Thammasat University, Pathum Thani 12120, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Taleb Ali Khalid</style></author><author><style face="normal" font="default" size="100%">Aarab Ahmed</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Medicinal Plants Adopted as Aphrodisiacs by Traditional Gynecologists in the Souss Massa Region</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Nil</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">406-413</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The population of southern Morocco particularly that of Souss Massa uses traditional empirical care, several specialties of traditional medicine exist in the region including women healers considered traditional gynecologists, these women used medicinal plants to treat female genital disorders. This study was carried out in order to collect information on the therapeutic practices and medicinal plants adopted and used by women healers named locally by &quot;ferraga&quot; or &quot;tachrift&quot; and &quot;tagouramt&quot; in the Souss Massa region (Agadir Idaoutanan, Inzegane Ait Meloul and Chtouka Ait Baha), in order to preserve and protect this invaluable inheritance from loss and overlook. Using questionnaires, a series of surveys were conducted during the years 2020-2021, on the one hand, among the population (sample of 279 people) to determine the importance of these women healers in the health sector of the region of these women healers, and on the other hand, a survey was conducted among these women healers to collect the recipes adopted in the treatment of female genital disorders especially infertility and sterility in these situations they prescribe aphrodiasitic plants. we recorded 59 species, divided into 28 botanical families, of which the Lamiaceae (15%) and the Apiaceae (12%) are the most widespread, and generally Leaves (35.38%) and seeds (18.48%) are the most used plant parts. These results show that the women healers have a very important place in the health service, especially they have a very interesting knowledge of the treatment of female genital disorders. The plants identified in this study could constitute a data base for further research in the field of phytochemistry and pharmacology.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">406</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Taleb Ali Khalid*,&amp;nbsp;Aarab Ahmed&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Equipe de Recherche en Biotechnologie et Génie des Biomolécules, Université Abdelmalek Essaadi FST tanger, MOROCCO.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Rismi Verawati</style></author><author><style face="normal" font="default" size="100%">Herland Satriawan</style></author><author><style face="normal" font="default" size="100%">Teresa Liliana Wargasetia</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Amalia Putri Lubis</style></author><author><style face="normal" font="default" size="100%">Bahrun</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Muhammad Thoriq Albari</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular Docking of Thaflavine from Camellia sinensis in Inhibiting B-Cell Lymphoma Through BCl2 Apoptosis Regulator: An In Silico Study</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Apoptosis Regulator BCl2</style></keyword><keyword><style  face="normal" font="default" size="100%">B-cell Lymphoma</style></keyword><keyword><style  face="normal" font="default" size="100%">Camellia sinensis.</style></keyword><keyword><style  face="normal" font="default" size="100%">In-Silico Thaflavine</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">500-505</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This study aims to analyze the potential of Thaflavine, a compound found in green tea (&lt;em&gt;Camellia&lt;/em&gt; sinensis), as an inhibitor in inhibiting B-cell lymphoma through its interaction with the BCl2 apoptosis regulator using an &lt;em&gt;in-silico&lt;/em&gt; approach. The research methodology involved the use of software tools such as PyMOL, PyRx, Protein Plus, and the Lepinski Rule. Through molecular docking analysis using PyMOL and PyRx, the findings of this study demonstrate significant interactions between Thaflavine and BCl2, with Binding Affinity values of -5.5, -4.6, and -4.6, and RMSD values of 0, 1.436, and 2.292. The analysis using Protein Plus indicates the presence of interactions between Thaflavine and BCl2. Additionally, the analysis using the Lepinski Rule of Five reveals that Thaflavine meets the criteria as a potential drug compound, with a molecular weight of 549, 9 hydrogen bond donors, 12 hydrogen bond acceptors, a log P value of -2.5, and a molar reactivity of 119.17. The findings of this study provide important contributions to the development of therapies for B-cell lymphoma through an &lt;em&gt;in-silico&lt;/em&gt; approach. However, further research is needed for &lt;em&gt;in vitro &lt;/em&gt;and in vivo validation.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">500</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Rahadian Zainul&lt;sup&gt;1,8,*&lt;/sup&gt;, Rismi Verawati&lt;sup&gt;1&lt;/sup&gt;, Herland Satriawan&lt;sup&gt;2&lt;/sup&gt;, Teresa Liliana Wargasetia&lt;sup&gt;3&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;4&lt;/sup&gt;, Amalia Putri Lubis&lt;sup&gt;1&lt;/sup&gt;, Bahrun&lt;sup&gt;5&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;6&lt;/sup&gt;, Muhammad Thoriq Albari&lt;sup&gt;7&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;9,10&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;11&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;12,13&lt;/sup&gt;, ANM Ansori&lt;sup&gt;9,10,11&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Institute of Ocean and Earth Sciences, Advanced Studies Complex, University Malaya, Kuala Lumpur, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Medicine, Universitas Maranatha Christian, Bandung, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Radiology, Universitas Awalbros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Doctoral student of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Hasanuddin, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Environmental and Policy Researcher, Environmental Science Program, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sarah S. Ismael</style></author><author><style face="normal" font="default" size="100%">Noor Ahmed M. Waheed</style></author><author><style face="normal" font="default" size="100%">Seema Mahmood Kasim</style></author><author><style face="normal" font="default" size="100%">Yasser Fakri Mustafa</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Novel Coumarin-Indole Hybrids as Cytotoxic Candidates:  Synthesis and Antiproliferative Activity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-breast cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Coumarin</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Indole</style></keyword><keyword><style  face="normal" font="default" size="100%">Michael addition</style></keyword><keyword><style  face="normal" font="default" size="100%">MTT</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">1105-1111</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Cancer is regarded as a nightmare for humanity and a challenging task for medical professionals. Twelve hydrides &lt;strong&gt;(2a-2l)&lt;/strong&gt;, made of trifunctionalized coumarin and various substituted indoles, were created in an effort to realize the hope of a cancer cure. The 4,5-dimethoxysalicylaldehyde and ethyl acetoacetate were combined in a Knoevenagel reaction to create the coumarin component. The construction of the indole component involved converting various aminoindoles through diazotization and Sandmeyer reactions to twelve substituted indoles &lt;strong&gt;(1a-1l)&lt;/strong&gt;. These two components were combined through a Michael addition reaction to create the desired hybrids. Investigating their spectra released from various spectroscopical instruments allowed researchers to determine the 2D molecular frameworks of these hybrids. Studying the survival of nine tumor cell types after treatment with the synthesized hybrids enabled researchers to estimate there in vitro impact as cytotoxic candidates. By checking the cell viability using an MTT marker, it was possible to see that this effect was antiproliferative. The cytotoxicity measurements, IC50 scores, revealed a number of intriguing facts. To start, the synthetic hybrids displayed a relatively similar cytotoxic pattern against the cancerous cell lines under investigation. Second, compared to hybrids with chloride, hydroxyl, or methoxy substituents, fluorinated hybrids are more toxic to cancerous cells. Finally, hybrids with indole substituted at position-6 &lt;strong&gt;(2i-2l) &lt;/strong&gt;have the highest cytotoxicity among those with indole functionalized at position-4 &lt;strong&gt;(2a-2d)&lt;/strong&gt; or position-5 &lt;strong&gt;(2e-2h)&lt;/strong&gt;. From these facts, the authors concluded that hybrids with indole substituted at position-4 can represent potential candidates as antiproliferative applicants. Moreover, hybrid &lt;strong&gt;2i &lt;/strong&gt;may serve as a valuable model for creating potent anti-breast cancer therapies.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1105</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Sarah S. Ismael*, Noor Ahmed M. Waheed, Seema Mahmood Kasim, Yasser Fakri Mustafa&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Pharmaceutical Chemistry, College of Pharmacy, University of Mosul, Mosul, IRAQ.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nur Fitri Hayati Melida Ritonga</style></author><author><style face="normal" font="default" size="100%">Ferdy R. Marpaung</style></author><author><style face="normal" font="default" size="100%">Hartono Kahar</style></author><author><style face="normal" font="default" size="100%">Nunuk Mardiana</style></author><author><style face="normal" font="default" size="100%">Yessy Puspitasari</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Performance Comparison of Urine Sediment Analytical Tool by  Flowcytometry and Digital Imaging with Standardized Manual  Microscopic Testing</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Digital imaging</style></keyword><keyword><style  face="normal" font="default" size="100%">Flowcytometry</style></keyword><keyword><style  face="normal" font="default" size="100%">Microscopic</style></keyword><keyword><style  face="normal" font="default" size="100%">Urine sediment</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">1189-1196</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Urine sediment examination provides numerous information about patient's kidney condition. Flowcytometry and digital imaging system could conduct automatic urine sediment analysis. Therefore, determining the diagnostic performance of the examination is very important in the management carried out by the clinician. This study aims to determine the diagnostic performance of urine flowcytometry and digital imaging sediment examination tools compared to manual microscopes that are standardized as gold standards. &lt;strong&gt;Methods: &lt;/strong&gt;This study is an analytical observational study with a cross-sectional approach on 92 urine samples of patients who attended the Internal Medicine Nephrology Polyclinic of Dr. Soetomo Academic Hospital Surabaya. The performance of flowcytometry and digital imaging methods is assessed by calculating sensitivity and specificity. Analysis of the suitability of each urine sediment parameter used Cohen's kappa. Urine sediment analysis with a light microscope was conducted with the Shih-Yung method as a gold standard. &lt;strong&gt;Results: &lt;/strong&gt;The erythrocyte parameters revealed a very favorable result with the concordance of the flowcytometry with the Shih-Yung method (κ=0.82) and fair results for WBC (κ=0.25), Epithelium (κ=0.57) and Cast (κ=0.27). At the same time, yeast had substantial conformity (κ=0.63). The digital imaging method showed substantive fit for WBC (κ=0.676), RBC (κ=0.621), fair for SEC (κ=0.42) and NSE (κ=0.24), moderate for Yeast (κ=0.45), and slight for Hyaline Cast (κ=0.074) and Path Cast (κ= 0.134) &lt;strong&gt;Conclusion: &lt;/strong&gt;The urine flowcytometry demonstrates better performance compatibility with a standardized manual microscope compared to urine digital imaging. However, pathological samples should still be verified with a manual microscope&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1189</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Nur Fitri Hayati Melida Ritonga&lt;sup&gt;1&lt;/sup&gt; , Ferdy R. Marpaung&lt;sup&gt;1&lt;/sup&gt; , Hartono Kahar&lt;sup&gt;1 &lt;/sup&gt;, Nunuk Mardiana&lt;sup&gt;2&lt;/sup&gt; , Yessy Puspitasari&lt;sup&gt;1,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Clinical Pathology Dr Soetomo Academic Hospital/Faculty of Medicine Universitas Airlangga Surabaya, INDONESIA. &lt;sup&gt;2&lt;/sup&gt;Department of Internal Medicine Dr Soetomo Academic Hospital/Faculty of Medicine Universitas Airlangga Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arnida Arnida</style></author><author><style face="normal" font="default" size="100%">Dian Kurnia</style></author><author><style face="normal" font="default" size="100%">Sutomo Sutomo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic Characteristics and Antioxidant Activity of Gendola Stem (Basella Rubra L.) Ethanol Extract from South Kalimantan</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant.</style></keyword><keyword><style  face="normal" font="default" size="100%">Basella rubra L.</style></keyword><keyword><style  face="normal" font="default" size="100%">Gendola</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognostic</style></keyword><keyword><style  face="normal" font="default" size="100%">Stem</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">329-332</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Gendola (&lt;em&gt;Basella rubra&lt;/em&gt; L.) is a medicinal plant native to South Kalimantan. Therefore, this research aims to determine the antioxidant activity of &lt;em&gt;B. rubra &lt;/em&gt;and the specific as well as nonspecific parameters of its ethanolic stem extract through pharmacognostic tests. &lt;strong&gt;Objective:&lt;/strong&gt; The specific parameters comprise of the extract composition, phytochemical screening, TLC profile, organoleptic, and microscopic variables. Meanwhile, drying shrinkage and ash content were the non-specific parameters.&lt;strong&gt; Materials and Methods: &lt;/strong&gt;The Indonesian Herbal Pharmacopoeia was used as a reference for the pharmacognostic test method. Also, the antioxidant activity was determined through the DPPH method, which was based on the IC&lt;sub&gt;50&lt;/sub&gt; value. &lt;strong&gt;Results:&lt;/strong&gt; A tasteless, brownish-purple powder with a characteristic smell, was obtained from the simple organoleptic assay while the epidermis, cortex, endodermis, pith, xylem, phloem, cambium, cell walls, stoma, epidermal, guard, and neighboring cells were observed through microscopic examinations. The &lt;em&gt;B. rubra&lt;/em&gt; stem contains phenolic compounds, flavonoids, steroids, tannins, and saponins. A good TLC profile was shown by the eluents of n-hexane: ethyl acetate (3:7) and chloroform: methanol (9:1). The &lt;em&gt;B. rubra&lt;/em&gt; simplicia stem had a water- and ethanol-soluble extract, drying shrinkage, total ash, and acid insoluble ash contents of 16.433% ± 0.252, 10.5% ± 0.173, 8.467% ± 0.153, 6.5% ± 0.1, and 0.517% ± 0.115, respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; Moreover, the pharmacognostic test results were acceptable. The B. rubra stem ethanol extract had an antioxidant activity of 344,096 ppm based on the IC&lt;sub&gt;50 &lt;/sub&gt;value.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">329</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Arnida Arnida*, Dian Kurnia, Sutomo Sutomo&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Pharmacy Study Program, Faculty of Mathematics and Natural Sciences, Lambung Mangkurat University Jl. A. Yani Km 36 Banjarbaru, South Kalimantan 70714, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Julio Luis Díaz-Uribe</style></author><author><style face="normal" font="default" size="100%">María Elena Salazar-Salvatierra</style></author><author><style face="normal" font="default" size="100%">Julio Reynaldo Ruiz-Quiroz</style></author><author><style face="normal" font="default" size="100%">Oscar Herrera- Calderon</style></author><author><style face="normal" font="default" size="100%">Eddie Loyola-Gonzales</style></author><author><style face="normal" font="default" size="100%">Freddy Emilio Tataje-Napuri</style></author><author><style face="normal" font="default" size="100%">José Francisco Kong-Chirinos</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Profile, Antioxidant and Antibacterial Activity of the Essential Oil of Luma Chequen (Molina) A. Gray from Peru</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial.</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Aromatic plant</style></keyword><keyword><style  face="normal" font="default" size="100%">Essential oil</style></keyword><keyword><style  face="normal" font="default" size="100%">Luma chequeen</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal plant</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">777-780</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background&lt;/strong&gt;: Luma chequen belongs to Myrtaceae family and it is known as “arrayan”. In the traditional medicine from Peru, L chequen is used as aromatic plant, anti-inflammatory and hypocholesterolemic. Objective: To determine the phytochemical profile, evaluate the antioxidant and the antibacterial activity of &lt;em&gt;L. chequen&lt;/em&gt; essential oil. &lt;strong&gt;Material and Methods&lt;/strong&gt;: In the analysis of the volatile components a Gas Chromatography coupled to Mass Spectrometry (GC-MS) was used to identify the content of terpenes and sesquiterpenes. 2,2-diphenyl-1-picrylhydrazyl (DPPH) was the method used to determine the antioxidant activity and obtain the half inhibitory concentration (IC&lt;sub&gt;50&lt;/sub&gt;). For the antibacterial activity, a colorimetric macrodilution method was carried out to evaluate the effect of the essential oil of &lt;em&gt;L. chequen&lt;/em&gt; against &lt;em&gt;Staphylococcus aureus&lt;/em&gt; ATCC 25923 and Escherichia coli ATCC 25922. &lt;strong&gt;Results:&lt;/strong&gt; The analysis by GC-MS showed two major components alpha-pinene (62.89%) followed by 1,8-cineole (11.94%), and propanoic acid, 2-methyl-, 2-methylpropyl ester with 8.67%. In the antioxidant activity against DPPH radical, the essential oil of &lt;em&gt;L. chequen&lt;/em&gt; showed an IC&lt;sub&gt;50&lt;/sub&gt; equivalent to124.60 ± 2.0 μg/mL. In the antibacterial activity, &lt;em&gt;L. chequen&lt;/em&gt; had an MIC (minimum inhibitory concentration) for &lt;em&gt;Staphylococcus aureus &lt;/em&gt;ATCC 25923 and Escherichia coli ATCC 25922 of 4.35 ± 0 μg/mL and 8.71 ± 0 μg/mL respectively. &lt;strong&gt;Conclusion&lt;/strong&gt;: &lt;em&gt;L. chequen &lt;/em&gt;presented monoterpene compounds as main phytoconstituents as well as antioxidant and antibacterial activity in vitro. The essential oil might be used as antimicrobial agent in the future overall against S. aureus.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">777</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Julio Luis Díaz-Uribe&lt;sup&gt;1&lt;/sup&gt;, María Elena Salazar-Salvatierra&lt;sup&gt;2&lt;/sup&gt;, Julio Reynaldo Ruiz-Quiroz&lt;sup&gt;2&lt;/sup&gt;, Oscar Herrera-Calderon&lt;sup&gt;3,*&lt;/sup&gt;, Eddie Loyola- Gonzales&lt;sup&gt;4&lt;/sup&gt;, Freddy Emilio Tataje- Napuri&lt;sup&gt;5&lt;/sup&gt;, José Francisco Kong- Chirinos&lt;sup&gt;6&lt;/sup&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Basic and Applied Chemistry Department, Faculty of Pharmacy and Biochemistry, Universidad Nacional Mayor de San Marcos, Lima 15001, PERU.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Institute for Research in Biological Chemistry, Microbiology and Biotechnology “Marco Antonio Garrido Malo”, Faculty of Pharmacy and Biochemistry, Universidad Nacional Mayor de San Marcos, Lima 15001, PERU.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacology, Bromatology and Toxicology, Faculty of Pharmacy and Biochemistry, Universidad Nacional Mayor de San Marcos, Lima, PERU.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmaceutical Science, Faculty of Pharmacy and Biochemistry, Universidad Nacional San Luis Gonzaga, Ica 11001, PERU.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Departamento de Ciencias Comunitarias, Facultad de Odontología, Universidad Nacional San Luis Gonzaga, Ica 11001, PERU.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Surgical Clinical Sciences, Faculty of Human Medicine, Universidad Nacional San Luis Gonzaga, Ica 11001, PERU.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohammed I. Khalid</style></author><author><style face="normal" font="default" size="100%">Ibrahim A.A Rahmaan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Prevalence of Legionella pneumophila in a Variety of  Environmental Water Systems</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">987-994</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The purpose of the current study is to isolate and identify &lt;em&gt;Legionella pneumophila&lt;/em&gt; by bacteriological and molecular methods from water and swab samples collected from a variety of water systems in Fallujah City, Iraq. A total of 227 samples were collected, including 146 swab samples and 81 of 1 L water samples. Bacteriological and molecular assays were performed compromised cultural, gram stain, a set of biochemical tests, and serological tests. The phenotypically validated isolates underwent a 16s rRNA gene by conventional PCR assays. The results showed 28 (12.33%) were positive with the presence of &lt;em&gt;legionella pneumophila&lt;/em&gt; isolates. including 5 (17.86%) positive isolates from water samples and 23 (82.14%) positive isolates from swabs. The current study showed that the majority of the water and swab samples were detected to be negative, but there is an appropriate exposure to this pathogen in the community. The diversity of the presence of these bacteria in several water systems, as well as the diversity in the use of multiple sources of water and exposure to them, leads to an increase in the potential risks of infection by &lt;em&gt;L. pneumophila.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">987</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Mohammed I. Khalid&lt;sup&gt;1,*&lt;/sup&gt;, Ibrahim A.A. Rahmaan&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biology, College of Science, University of Anbar, Anbar, IRAQ.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;College of Applied Sciences, University of Fallujah, Fallujah, IRAQ.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Meilla Dwi Andrestian</style></author><author><style face="normal" font="default" size="100%">Meitria Syahadatina Noor</style></author><author><style face="normal" font="default" size="100%">Resa Ana Dina</style></author><author><style face="normal" font="default" size="100%">Ayunina Rizky Ferdina</style></author><author><style face="normal" font="default" size="100%">Zulfiana Dewi</style></author><author><style face="normal" font="default" size="100%">Niken Widyastuti Hariati</style></author><author><style face="normal" font="default" size="100%">Purnawati Hustina Rachman</style></author><author><style face="normal" font="default" size="100%">Muhammad Irwan Setiawan</style></author><author><style face="normal" font="default" size="100%">Windy Tri Yuana</style></author><author><style face="normal" font="default" size="100%">Ali Khomsan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Qualitative Study on Adolescent Marriage and The Risk of  Stunting in South Kalimantan</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adolescent marriage</style></keyword><keyword><style  face="normal" font="default" size="100%">Qualitative investigation</style></keyword><keyword><style  face="normal" font="default" size="100%">Stunting</style></keyword><keyword><style  face="normal" font="default" size="100%">Toddler feeding pattern</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">1016-1023</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; An exploratory qualitative investigation to determine the causes of adolescent marriage, analyze the effect of early marriage on stunting, and analyze the food patterns of toddlers in adolescent marriage in South Kalimantan, Indonesia.&lt;strong&gt; Method:&lt;/strong&gt; The method used is phenomenology using the FGD system and in-depth interviews. Participants include the FGD informants from the Family Planning Regional Apparatus Organization, the Office of Women's Empowerment and Child Protection and the Office of Religious Affairs from 13 Regencies/ Cities in South Kalimantan. In-depth interview informants were adolescent marriage offenders and their parents, adolescent pregnant women, midwives, integrated health service post cadres, and community leaders each taken from three Regencies/ Cities. &lt;strong&gt;Results: &lt;/strong&gt;There are not many formal adolescent marriages because they have to get a recommendation from the Religious Courts. Adolescent marriages mostly occur through informal marriages. The high rate of early marriage in South Kalimantan Province is caused by culture and weak enforcement of the rules. The incidence of adolescent marriage is caused by promiscuity and information. Meanwhile, adolescent marriage is mostly due to economic motives and limited education facilities in rural areas. Adolescent marriage is not closely related to the incidence of stunting, but low education can be a factor in the inability of parents to provide good parenting, especially feeding pratice. &lt;strong&gt;Conclusions:&lt;/strong&gt; Adolescent marriages appear to be triggered by economic motives and teenagers' desires, as well as driven by economic conditions, social influences, and a lack of encouragement to complete formal education. It was observed that stunting is more common among toddlers with adolescent mothers than toddlers with adult mothers. There is a poor feeding parenting pattern of toddlers with adolescent parents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1016</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Meilla Dwi Andrestian&lt;sup&gt;1,&lt;/sup&gt;*, Meitria Syahadatina Noor&lt;sup&gt;2&lt;/sup&gt; , Resa Ana Dina&lt;sup&gt;3&lt;/sup&gt; , Ayunina Rizky Ferdina&lt;sup&gt;4&lt;/sup&gt; , Zulfiana Dewi&lt;sup&gt;5&lt;/sup&gt; , Niken Widyastuti Hariati&lt;sup&gt;6&lt;/sup&gt; , Purnawati Hustina Rachman&lt;sup&gt;7&lt;/sup&gt; , Muhammad Irwan Setiawan&lt;sup&gt;8&lt;/sup&gt; , Windy Tri Yuana&lt;sup&gt;9&lt;/sup&gt; , Ali Khomsan&lt;sup&gt;10&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Nutrition, Polytechnic of Health Ministry of Health, Banjarbaru, South Kalimantan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Medicine, University of Lambung Mangkurat, Banjarmasin, South Kalimantan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Community Nutrition, Faculty of Human Ecology, IPB University, Bogor, West Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;National Research and Innovation Agency, Bogor, West Jawa, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Nutrition, Polytechnic of Health Ministry of Health, Banjarbaru, South Kalimantan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Nutrition, Polytechnic of Health Ministry of Health, Banjarbaru, South Kalimantan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Community Nutrition, Faculty of Human Ecology, IPB University, Bogor, West Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Faculty of Medicine, University of Lambung Mangkurat, Banjarmasin, South Kalimantan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;National Research and Innovation Agency, Bogor, West Jawa, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Department of Community Nutrition, Faculty of Human Ecology, IPB University, Bogor, West Java, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arti Gautam</style></author><author><style face="normal" font="default" size="100%">Lal Chand Pal</style></author><author><style face="normal" font="default" size="100%">Ch. V Rao</style></author><author><style face="normal" font="default" size="100%">Vikas Kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Role of Indian Magical Herb Selaginella bryopteris L. (Selaginaceae) in Pharmacotherapeutic Perspective: An Overview</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biflavonoid</style></keyword><keyword><style  face="normal" font="default" size="100%">S. bryopteris L.</style></keyword><keyword><style  face="normal" font="default" size="100%">Sanjeevni</style></keyword><keyword><style  face="normal" font="default" size="100%">Selaginaceae</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">14-20</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This review involves the medicinal as well as therapeutic applications of Sanjeevni (&lt;em&gt;Selaginella bryopteris&lt;/em&gt; L.) in curtailing different types of acute and chronic maladies. The magical herb (&lt;em&gt;Selaginella bryopteris&lt;/em&gt;) is utilized for its resurrecting and medicinal properties in various regions of the world. &lt;em&gt;S. bryopteris&lt;/em&gt; based formulations have been widely used in folk medicine to treat spermatorrhoea, colitis, epilepsy, leucorrhoea, urinary tract infections, fever, venereal illnesses, constipation, beri-beri, cancer, and many other ailments. The medicinal and pharmacological effects of &lt;em&gt;S. bryopteris &lt;/em&gt;have been extensively studied in recent years, employing a variety of&lt;em&gt; in vivo&lt;/em&gt; and&lt;em&gt; in vitro&lt;/em&gt; models and clinical studies. Many biochemical and pharmacological studies on &lt;em&gt;Selaginella bryopteris&lt;/em&gt; have been conducted, and many of its traditional applications have been validated scientifically. Different biological activities are concerned with it, like anti-bacterial, growth-promoting, anti-protozoan, relief from heat stroke and the burning sensation during urination, anti-stress cell death, memory improvement, relief from stomach-aches, anti-hyperglycemic activity, and anti-depressant activity. S. bryopteris is undeniably one of the most significant plants owing to its enormous pharmacological and therapeutic potential. On the other hand, several information gaps found in this article might spur fresh academic and R&amp;amp;D efforts to produce S. bryopteris-based herbal medications and nutraceuticals.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">14</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Arti Gautam&lt;sup&gt;1&lt;/sup&gt;, Lal Chand Pal&lt;sup&gt;2&lt;/sup&gt;, Ch. V Rao&lt;sup&gt;2&lt;/sup&gt;, Vikas Kumar&lt;sup&gt;1*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Sciences, Sam Higginbottom University of Agriculture, Technology &amp;amp; Sciences (SHUATS), Naini, Prayagraj, Uttar Pradesh, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacology Division, National Botanical Research Institute (CSIR), Lucknow, Uttar Pradesh, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Rismi Verawati</style></author><author><style face="normal" font="default" size="100%">Ritbey Ruga</style></author><author><style face="normal" font="default" size="100%">Muhammad Arya Ghifari</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Putri Azhari</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Stimulation of Emodin from Aloe Vera on Protein Kinase PIM1 in the Central Nervous System Through In Silico Analysis</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Central Nervous System</style></keyword><keyword><style  face="normal" font="default" size="100%">Emodin</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular Docking.</style></keyword><keyword><style  face="normal" font="default" size="100%">PIM1 Kinase</style></keyword><keyword><style  face="normal" font="default" size="100%">Stimulation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">587-592</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This study aims to investigate the potential of Emodin, a compound found in Aloe vera, as a stimulator of Protein Kinase PIM1 in the central nervous system using an &lt;em&gt;in-silico &lt;/em&gt;approach. The research method involves the use of software such as Pymol, Pyrex, Protein Plus, and Lepinski Rule. Firstly, the protein structure of the target Protein Kinase PIM1 was obtained from a protein database and prepared using Pymol. Next, the molecular structure of Emodin was imported into Pyrex and subjected to geometry optimization. Docking analysis using Pymol was performed to predict the molecular interactions between Emodin and Protein Kinase PIM1. Additionally, RMSD analysis was conducted to evaluate the stability of the protein-ligand complex formed. The docking analysis results showed that Emodin exhibited significant Binding Affinity, with values of -8.4, -8.3, and -8.2, indicating a strong affinity between Emodin and Protein Kinase PIM1. The RMSD analysis indicated the stability of the protein-ligand complex, with RMSD values of 0, 1.101, and 1.122. Furthermore, analysis using Protein Plus revealed the presence of interactions between Emodin and Protein Kinase PIM1 through hydrogen bonding and hydrophobic contacts. The results of the Lepinski Rule analysis demonstrated that Emodin fulfilled several important criteria in drug design, including a molecular weight of 270, 3 hydrogen bond donors, 5 hydrogen bond acceptors, a log p value of 1.887220, and a molar reactivity of 64.480385. These findings indicate the potential of Emodin as a stimulator of Protein Kinase PIM1 in the central nervous system and provide an important foundation for the development of potential therapies for central nervous system-related disorders.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">587</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Rahadian Zainul&lt;sup&gt;1,2,*&lt;/sup&gt;, Rismi Verawati&lt;sup&gt;3&lt;/sup&gt;, Ritbey Ruga&lt;sup&gt;4&lt;/sup&gt;, Muhammad Arya Ghifari&lt;sup&gt;5&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;6&lt;/sup&gt;, Putri Azhari&lt;sup&gt;7&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;8,9&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;10&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;11,12&lt;/sup&gt;, ANM Ansori&lt;sup&gt;8,9,10&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Mulawarman, Samarinda, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Radiology, Universitas Awalbros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Agricultural Technology, Faculty of Agricultural Technology, Universitas Andalas, Padang, West Sumatra, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Anni Faridah</style></author><author><style face="normal" font="default" size="100%">Rismi Verawati</style></author><author><style face="normal" font="default" size="100%">Budhi Oktavia</style></author><author><style face="normal" font="default" size="100%">Musa Ghufron</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Muhammad Raffi Ghifari</style></author><author><style face="normal" font="default" size="100%">Linda Rosalina</style></author><author><style face="normal" font="default" size="100%">Putri Azhari</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Study on the Inhibition of Sinensetin Extract from Cat's Whiskers Plant (Orthosiphon aristatus) on ATP Binding Cassette Sub-Family G Member 2 in Uric Acid</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ATP Binding Cassette</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword><keyword><style  face="normal" font="default" size="100%">Orthosiphon aristatus</style></keyword><keyword><style  face="normal" font="default" size="100%">Sinensetin</style></keyword><keyword><style  face="normal" font="default" size="100%">Uric Acid.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">506-511</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;This study aims to investigate the potential of sinensetin, a compound found in the Cat's Whiskers plant (&lt;em&gt;Orthosiphon aristatus&lt;/em&gt;), as an inhibitor in inhibiting uric acid through its interaction with ATP Binding Cassette Sub-Family G Member 2 (ABCG2). The &lt;em&gt;in-silico &lt;/em&gt;approach was employed using software tools such as Pymol, PyRx, Protein Plus, and Lepinski Rule. The results of molecular docking analysis using PyRx demonstrated significant interactions between sinensetin and ABCG2, with Binding Affinity values of -6.8, -6.6, and -6.6, and RMSD values of 0, 0.785, and 1.379. The analysis using Protein Plus confirmed the interaction between sinensetin and ABCG2, supporting the previous docking findings. Furthermore, the evaluation of pharmacokinetic parameters using the Lepinski Rule of Five revealed that sinensetin meets the criteria as a potential drug compound, with a molecular weight of 372, no hydrogen bond donors, seven hydrogen bond acceptors, a log P value of 3.345, and a molar reactivity of 98.5. This research provides new insights into the development of uric acid therapy through an &lt;em&gt;in-silico &lt;/em&gt;approach, and these findings can serve as a basis for further research involving in vitro and in vivo validation.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">506</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Anni Faridah&lt;sup&gt;1&lt;/sup&gt;, Rismi Verawati&lt;sup&gt;2&lt;/sup&gt;, Budhi Oktavia&lt;sup&gt;2&lt;/sup&gt;, Musa Ghufron&lt;sup&gt;3&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;4&lt;/sup&gt;, Muhammad Raffi Ghifari&lt;sup&gt;5&lt;/sup&gt;, Linda Rosalina&lt;sup&gt;6&lt;/sup&gt;, Putri Azhari&lt;sup&gt;7&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;2,8,*&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;9,10&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;11&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;12,13&lt;/sup&gt;, ANM Ansori&lt;sup&gt;9,10,11&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Tourism and Hospitality, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Public Health and Community Medicine, Faculty of Medicine, Universitas Muhammadiyah Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Radiology, Universitas Awalbros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Makeup and Beauty, Faculty of Tourism and Hospitality, Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Agricultural Technology, Faculty of Agricultural Technology, Universitas Andalas, Padang, West Sumatra, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Himyatul Hidayah</style></author><author><style face="normal" font="default" size="100%">Surya Amal</style></author><author><style face="normal" font="default" size="100%">Nia Yuniarsih</style></author><author><style face="normal" font="default" size="100%">Farhamzah</style></author><author><style face="normal" font="default" size="100%">Anggun Hari Kusumawati</style></author><author><style face="normal" font="default" size="100%">Neni Sri Gunarti</style></author><author><style face="normal" font="default" size="100%">Ermi Abriyani</style></author><author><style face="normal" font="default" size="100%">Iin Lidia Putama Mursal</style></author><author><style face="normal" font="default" size="100%">Adinda Khansa Sundara</style></author><author><style face="normal" font="default" size="100%">Maulana Yusuf Alkandahri</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sun Protection Factor Activity of Jamblang Leaves Serum Extract (Syzygium cumini)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Serum</style></keyword><keyword><style  face="normal" font="default" size="100%">Sun protection factor</style></keyword><keyword><style  face="normal" font="default" size="100%">Syzygium cumini</style></keyword><keyword><style  face="normal" font="default" size="100%">Ultraviolet.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">134-140</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;The development of serum preparations containing natural ingredients for sun protection is growing rapidly. Jamblang (&lt;em&gt;Syzygium cumini&lt;/em&gt;) leaves are rich in phenolic compounds that can inhibit free radicals causing premature aging. Therefore, this study aims to determine the potential of &lt;em&gt;S. cumin&lt;/em&gt;i serum extract as sun protection. &lt;strong&gt;Methods:&lt;/strong&gt; The extract was prepared and included in the serum base. The formulations were evaluated for rheological, pH, dispersion coefficient, and stability examinations. Furthermore, Sun Protection Factor was tested using a UV-Vis spectrophotometer. &lt;strong&gt;Results: &lt;/strong&gt;The test of phytochemical compounds showed the presence of alkaloids, flavonoids, polyphenols, tannins, saponins, quinones, monoterpenoids, sesquiterpenoids, triterpenoids, and steroids. The result also showed that all serum formulations met the predetermined requirements. Furthermore, the extract has protective activity against ultraviolet rays, which was indicated by the SPF value. The higher the dose of &lt;em&gt;S. cumini&lt;/em&gt; extracts in the serum formulation, the higher the value obtained. Formulations 1, 2, and 3 have SPF of 9.35±0.11, 13.26±0.16, and 26.05±0.31, respectively. This indicates that they all met the Indonesian National Standard, that a sun protection preparation must have a minimum protection factor of 4. &lt;strong&gt;Conclusion: &lt;/strong&gt;&lt;em&gt;S. cumini&lt;/em&gt; extract serum has the potential to be developed as a new sun protection agent against ultraviolet radiation. However, further studies are still needed to determine the mechanism of its constituent active compounds.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">134</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Himyatul Hidayah&lt;sup&gt;1&lt;/sup&gt;, Surya Amal&lt;sup&gt;1&lt;/sup&gt;, Nia Yuniarsih&lt;sup&gt;1&lt;/sup&gt;, Farhamzah&lt;sup&gt;1&lt;/sup&gt;, Anggun Hari Kusumawati&lt;sup&gt;1&lt;/sup&gt;, Neni Sri Gunarti&lt;sup&gt;1&lt;/sup&gt;, Ermi Abriyani&lt;sup&gt;1&lt;/sup&gt;, Iin Lidia Putama Mursal&lt;sup&gt;1&lt;/sup&gt;, Adinda Khansa Sundara&lt;sup&gt;2&lt;/sup&gt;, Maulana Yusuf Alkandahri&lt;sup&gt;1,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Pharmacy, Universitas Buana Perjuangan Karawang, Karawang, West Java, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Student of Pharmacy, Faculty of Pharmacy, Universitas Buana Perjuangan Karawang, Karawang, West Java, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sandy Novryanto Sakati</style></author><author><style face="normal" font="default" size="100%">Anwar Mallongi</style></author><author><style face="normal" font="default" size="100%">Erniwati Ibrahim</style></author><author><style face="normal" font="default" size="100%">Budimawan</style></author><author><style face="normal" font="default" size="100%">Stang</style></author><author><style face="normal" font="default" size="100%">Sukri Palutturi</style></author><author><style face="normal" font="default" size="100%">Maria Kanan</style></author><author><style face="normal" font="default" size="100%">Herawati</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Utilization of Rainwater as Consumable Water with Rainwater Harvesting Methods: A Literature Review</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Consumable</style></keyword><keyword><style  face="normal" font="default" size="100%">Harvesting</style></keyword><keyword><style  face="normal" font="default" size="100%">Rainwater</style></keyword><keyword><style  face="normal" font="default" size="100%">Utilization</style></keyword><keyword><style  face="normal" font="default" size="100%">Water Quality</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><pages><style face="normal" font="default" size="100%">1254-1257</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Water demand is expected to increase in all sectors. Rainwater can be a solution to the lack of the clean water crisis. The quality of rainwater harvested is highly dependent on the rainwater harvesting system. &lt;strong&gt;Methods: &lt;/strong&gt;This literature review is a narrative review using sources from the Scopus and Pubmed databases. The keywords used were utilization, rainwater, and rainwater harvesting methods. Of the 30 references identified in the search phase, ten were eligible for inclusion in this review. &lt;strong&gt;Results:&lt;/strong&gt; Harvested rainwater can be used for multiple purposes such as watering plants, washing, bathing, and even cooking if the water quality meets health standards. There are three fundamental components that should be present within the rainwater harvesting system: 1) a rainwater pipe that traps water, e.g., utilizing the shape of the roof surface, 2) a water distribution system, i.e., a system that transports water from the roof to the superficies through a gutter, and 3) a reservoir that stores rainwater such as barrels, tubs, or ponds. &lt;strong&gt;Conclusions:&lt;/strong&gt; Water conservation efforts are needed to meet the demand for water in the face of increasingly limited supply. Harvesting rainwater is one of the methods of water conservation that can be carried out by each household of the community to collect raw rainwater for consumption and use. If rainwater harvesting is practiced in a sustainable manner, it will help maintain water and environmental sustainability, thus supporting the livelihood of present and future generations.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">1254</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sandy Novryanto Sakati&lt;sup&gt;1,3&lt;/sup&gt;, Anwar Mallongi&lt;sup&gt;2,*&lt;/sup&gt;, Erniwati Ibrahim&lt;sup&gt;2&lt;/sup&gt; , Budimawan&lt;sup&gt;2&lt;/sup&gt; , Stang&lt;sup&gt;2&lt;/sup&gt; , Sukri Palutturi&lt;sup&gt;2&lt;/sup&gt; , Maria Kanan&lt;sup&gt;3&lt;/sup&gt; , Herawati&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Doctoral student, Public Health Sciences, Hasanudin University Makassar, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Public Health, Faculty of Public Health Sciences, Universitas Hasanuddin, Makassar, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Public Health, Faculty of Public Health Sciences, University of Tompotika, Luwuk Banggai, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ponco Birowo</style></author><author><style face="normal" font="default" size="100%">Nurhuda Sahar</style></author><author><style face="normal" font="default" size="100%">R. Muharam</style></author><author><style face="normal" font="default" size="100%">Dwi Ari Pujianto</style></author><author><style face="normal" font="default" size="100%">Rosalina Thuffi</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Conny Riana Tjempakasari</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Analysis of LH Receptor Expression in the Testes of Infertile Azoospermic Non-Obstructive (NOA) Men at High Serum Prolactin Concentrations</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hyperprolactinemia</style></keyword><keyword><style  face="normal" font="default" size="100%">LH receptor expression</style></keyword><keyword><style  face="normal" font="default" size="100%">Male infertility</style></keyword><keyword><style  face="normal" font="default" size="100%">Non obstructive azoospermia (NOA).</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">462-468</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Hyperprolactin is one of the endocrine disorders that causes male infertility (11%). The mechanism is not widely known; it is thought to occur through disruption of LH receptor activity on germ cells. &lt;strong&gt;Objective:&lt;/strong&gt; The aim of study to compare the level of prolactin secretion with receptor expression in non-azoospermic infertile men (NOA). &lt;strong&gt;Methods&lt;/strong&gt;: During the period from July 2019 to July 2021, 40 samples of testicular tissue and serum were obtained from infertile NOA men, aged 25-50 years who were recruited from Ciptomangunkusumo Hospital (RSCM) Jakarta, Faculty of Medicine, Universitas Indonesia and Bunda Hospital Jakarta. Subjects were divided into 4 groups based on prolactin levels (20 ng/ml, 20-50 ng/ml, 50-100 ng/ml and 100ng/ml). This group was tested for significance between groups and continued with a correlation test with the level of LH receptor expression. &lt;strong&gt;Results&lt;/strong&gt;: ANOVA test showed a significant decrease in LH receptor expression between prolactin levels &amp;lt; 20 ng/mL with levels of 50-100 ng/ml and prolactin levels &amp;gt; 100 ng/ml (P &amp;lt; 0.05). Furthermore, the results of the correlation test showed a significant decrease between prolactin levels and LH receptor expression (P &amp;lt; 0.05). &lt;strong&gt;Conclusion&lt;/strong&gt;: The higher the level of prolactin secretion in this sample, there is a decrease in LH receptor expression, so that testosterone production decreases and the spermatogenesis process will be disrupted.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">462</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ponco Birowo&lt;sup&gt;1&lt;/sup&gt;, Nurhuda Sahar&lt;sup&gt;2&lt;/sup&gt;, R. Muharam&lt;sup&gt;3&lt;/sup&gt;, Dwi Ari Pujianto&lt;sup&gt;2&lt;/sup&gt;, Rosalina Thuffi&lt;sup&gt;4&lt;/sup&gt;, Kusmardi Kusmardi&lt;sup&gt;5-8,*&lt;/sup&gt;, Conny Riana Tjempakasari&lt;sup&gt;9&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Urology, Faculty of Medicine, Universitas Indonesia Jl. Salemba Raya No.6, Jakarta, 10430, Jakarta, Indonesia, 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biology, Faculty of Medicine, University of Indonesia, Jl. Salemba Raya No.6, Jakarta, 10430, Jakarta, Indonesia, 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Obstetrics and Gynecology, Faculty of Medicine, Universitas Indonesia Jl. Salemba Raya No.6, Jakarta, 10430, Jakarta, Indonesia, 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Magister Program Biomedical sciences, Faculty of Medicine, Universitas Indonesia Jl. Salemba Raya No.6, Jakarta, 10430, Jakarta, Indonesia, 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Anatomic Pathology, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya No.6, Jakarta, 10430, Jakarta, Indonesia, 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Drug Development Research Cluster, Indonesia Medical Educational and Research Institute, Jl. Salemba Raya No.6, Jakarta 10340, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Human Cancer Research Cluster, Indonesia Medical Educational and Research Institute, Jl. Salemba Raya No.6, Jakarta 10340, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Doctoral Programme Study of Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, Jl. Salemba Raya No.6, Jakarta, 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Department of Microbiology Faculty of Medicine, Universitas Indonesia, Jakarta, 10430, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">N Aji</style></author><author><style face="normal" font="default" size="100%">S Kumala</style></author><author><style face="normal" font="default" size="100%">E Mumpuni</style></author><author><style face="normal" font="default" size="100%">D Rahmat</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antibacterial Activity and Active Fraction of Zingiber officinale Roscoe, Zingiber montanum (J.Koenig) Link ex A., and Zingiber zerumbet (L.) Roscoe ex Sm. Against Propionibacterium acnes</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">103-111</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Propionibacterium acnes is a commensal bacteria that play a role in developing acne vulgaris on the skin. Antibacterial activity assay in the last decades have shown that Propionibacterium acnes is resistant to several antibiotics. Potential zingiber genera such as &lt;em&gt;Z. officinale&lt;/em&gt;, Z. montanum, and&lt;em&gt; Z. zerumbet&lt;/em&gt; have potential as antibacterial. &lt;strong&gt;Objective:&lt;/strong&gt; This study aims to compare the antibacterial activity of &lt;em&gt;Z. officinale,&lt;/em&gt; &lt;em&gt;Z. montanum&lt;/em&gt; and Z. zerumbet against Propionibacterium acnes, the active fraction, and the components of the active fraction of the plant. &lt;strong&gt;Materials and Methods&lt;/strong&gt;: Antibacterial activity test using agar diffusion method, extracts with high antibacterial activity were partitioned with water: n-hexane, n-hexane: methanol, water: ethyl acetate. The fraction was tested for antibacterial activity against P. acnes. The active fraction obtained was identified for its phytochemical content using TLC and GC-MS methods.&lt;strong&gt; Results:&lt;/strong&gt; The results of the antibacterial activity test of&lt;em&gt; Z. officinale &lt;/em&gt;extract had a larger inhibition zone. The test results of the active fraction&lt;em&gt; Z. officinale&lt;/em&gt; had a higher activity than the extract. The results of screening using the GC-MS method obtained that the main components identified from &lt;em&gt;Z. officinale&lt;/em&gt; were volatile oil components (α-curcumene, α-zingiberene and zingerone) and oleoresin (6-shogaol). &lt;strong&gt;Conclusion: &lt;/strong&gt;Extracts of &lt;em&gt;Z. officinale&lt;/em&gt;, &lt;em&gt;Z. montanum &lt;/em&gt;and &lt;em&gt;Z. zerumbet &lt;/em&gt;had antibacterial activity against P. acnes. The highest antibacterial activity in&lt;em&gt; Z. officinal&lt;/em&gt;e both extract and ethyl acetate fraction which is known to contain terpenoids and oleoresin compounds (6-shogaol).&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Key words&lt;/strong&gt;: Antibacterial, Zingiber officinale, Zingiber montanum, Zingiber zerumbeth, Propionibacterium acnes.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">103</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;N Aji&lt;sup&gt;1,2*&lt;/sup&gt;, S Kumala&lt;sup&gt;1*&lt;/sup&gt;, E Mumpuni&lt;sup&gt;1&lt;/sup&gt;, D Rahmat&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Pharmacy, Pancasila University, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacy, Poltekkes Kemenkes Tasikmalaya, Tasikmalaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tiana Milanda</style></author><author><style face="normal" font="default" size="100%">Raden Maya Febriyanti</style></author><author><style face="normal" font="default" size="100%">Arif Satria Wira Kusuma</style></author><author><style face="normal" font="default" size="100%">Ajeng Diantini</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antibacterial and Cytotoxic Activity of Selected Raw-Consumed Vegetables in West Java, Indonesia</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Edible plants</style></keyword><keyword><style  face="normal" font="default" size="100%">West Java</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">289-295</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Raw-consumed vegetables, known as lalapan, is famous among Sundanese community in West Java because of their heath benefits. In the present study, nine selected raw-consumed vegetables, namely &lt;em&gt;Vigna unguiculata, Ocimum tenuiflorum Linn, Psophocarpus tetragonolobus, Etlingera elatior, Abelmoschus esculentus, Oenanthe javanica, Centella asiatica, Pluchea indica&lt;/em&gt; and &lt;em&gt;Pilea trinervia &lt;/em&gt;were screened for their antibacterial and cytotoxic activity. Antibacterial activity test were conducting using disc diffusion method against Serratia marcescens, Escherichia coli, Enterobacter cloacae. Whereas, the cytotoxic activity were examined using WST assay against lung cancer cell line A549. For the antibacterial activity, this study finds that &lt;em&gt;Ocimum tenuiflorum, Etlingera elatior and Pluchea indica&lt;/em&gt; have highest inhibition zone against tested bacteria. Furthemore, the results of the cytotoxicity assay indicated that among the nine plants tested, five plants showed IC&lt;sub&gt;50&lt;/sub&gt; &amp;lt; 20 μg/mL, including &lt;em&gt;Vigna unguiculata, Ocimum tenuiflorum Linn, Etlingera elatior, Centella asiatica&lt;/em&gt; and &lt;em&gt;Pilea trinervia &lt;/em&gt;with the IC&lt;sub&gt;50 &lt;/sub&gt;value 13.71 μg/mL, 7.43 μg/mL, 12.45 μg/mL, 5.51 μg/mL and 18.84 μg/mL respectively.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">289</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Tiana Milanda&lt;sup&gt;1&lt;/sup&gt;, Raden Maya Febriyanti&lt;sup&gt;2,*&lt;/sup&gt;, Arif Satria Wira Kusuma&lt;sup&gt;3&lt;/sup&gt;, Ajeng Diantini&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Associate Professor at Department of Pharmaceutical Biology, Faculty of Pharmacy, Padjadjaran University, Jatinangor, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Doctor in the field of Ethnopharmacy and Lecturer at Department of Pharmaceutical Biology, Faculty of Pharmacy, Padjadjaran University, Jatinangor, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;PhD Student in Molecular Bioscience Program Rutgers the State University of New Jersey, United States of America and lecturer at Department of Pharmaceutical Biology, Faculty of Pharmacy, Padjadjaran University, Jatinangor, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Professor in Pharmacology and Clinical Pharmacy at Faculty of Pharmacy, Padjadjaran University, Jatinangor, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Asep Sukohar</style></author><author><style face="normal" font="default" size="100%">Suharyani</style></author><author><style face="normal" font="default" size="100%">Sutyarso</style></author><author><style face="normal" font="default" size="100%">Hendri Busman</style></author><author><style face="normal" font="default" size="100%">Nuning Nurcahyani</style></author><author><style face="normal" font="default" size="100%">Evi Kurniawaty</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antioxidant and Cytotoxic Activities of Melinjo (Gnetum gnemon L.) Seed Fractions on HeLa Cell Line an In Vitro</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxic</style></keyword><keyword><style  face="normal" font="default" size="100%">HeLa.</style></keyword><keyword><style  face="normal" font="default" size="100%">Melinjo</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">559-564</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Medicinal plants have been investigated for possible anti-cancer effects. One of them is&lt;em&gt; Gnetum gnemon&lt;/em&gt; L (melinjo). This study aims determined&lt;em&gt; in vitro &lt;/em&gt;antioxidant activity and the cytotoxic effects of polar, semipolar and non polar melinjo seed fractions againts HeLa cell line. &lt;strong&gt;Methods: &lt;/strong&gt;The melinjo seed were extracted with ethanol as a solvent. Then, the fractionation was done using liquidliquid extraction method with three different polarity solvent. Cytotoxic activity was carried out using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) colorimetric assay in HeLa cell lines at concentrations ranging from 25 to 400 μg/mL. Antioxidant activity was determined by the diphenyl picryl hidrazil (DPPH) radical scavenging method. &lt;strong&gt;Results: &lt;/strong&gt;Phytochemical screening indicated the presence of phyto-constituents like flavonoids, terpenoid and tanin. The DPPH scavenging activity by the melinjo seed aqueous, ethyl acetate and N-hexane fraction was 733,12 ± 18,95 μg/mL; 68,40 ± 1,9 μg/mL and 2035,70 ± 65,59 μg/mL, respectively. The cytotoxic activity of the melinjo seed fractions showed that the ethyl acetate was the most active fraction against HeLa cell line with IC&lt;sub&gt;50&lt;/sub&gt; value 45,27 μg/mL.&lt;strong&gt; Conclusion:&lt;/strong&gt; In this study, we have observed that the melinjo seed fractions exhibited antioxidant and cytotoxic activity against HeLa cell lines. This is presumably due to the content of phytochemicals and stilbenoids such as resveratrol and gnetin C. Melinjo seeds are more potent as anticancer Compared with other plants that also contain RSV such as grape extract (&lt;em&gt;Vitis vinifera&lt;/em&gt; L.) against lung cancer cells (A549). From the three fractions, the ethyl acetate fraction had the highest antioxidant and cytotoxic effect compared to the water and n-hexane fractions. &lt;em&gt;Gnetum gnemon&lt;/em&gt; L. can be considered as a potential source of anticancer agents. However, more research is needed to determine the mechanism of action.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><accession-num><style face="normal" font="default" size="100%">11</style></accession-num><section><style face="normal" font="default" size="100%">559</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Asep Sukohar1, Suharyani&lt;sup&gt;1,2,*&lt;/sup&gt;, Sutyarso&lt;sup&gt;2&lt;/sup&gt;, Hendri Busman&lt;sup&gt;2&lt;/sup&gt;, Nuning Nurcahyani&lt;sup&gt;2&lt;/sup&gt;, Evi Kurniawaty&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Medicine, University of Lampung, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Magister Biology, Faculty of Mathematics and Natural Sciences, University of Lampung, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">ANM Ansori</style></author><author><style face="normal" font="default" size="100%">VD Kharisma</style></author><author><style face="normal" font="default" size="100%">AA Parikesit</style></author><author><style face="normal" font="default" size="100%">FA Dian</style></author><author><style face="normal" font="default" size="100%">RT Probojati</style></author><author><style face="normal" font="default" size="100%">M Rebezov</style></author><author><style face="normal" font="default" size="100%">P Scherbakov</style></author><author><style face="normal" font="default" size="100%">P Burkov</style></author><author><style face="normal" font="default" size="100%">G Zhdanova</style></author><author><style face="normal" font="default" size="100%">A Mikhalev</style></author><author><style face="normal" font="default" size="100%">Y Antonius</style></author><author><style face="normal" font="default" size="100%">MRF Pratama</style></author><author><style face="normal" font="default" size="100%">NI Sumantri</style></author><author><style face="normal" font="default" size="100%">TH Sucipto</style></author><author><style face="normal" font="default" size="100%">R Zainul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bioactive Compounds from Mangosteen (Garcinia mangostana L.) as an Antiviral Agent via Dual Inhibitor Mechanism against SARSCoV- 2: An In Silico Approach</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">85-90</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Severe acute respiratory syndrome coronavirus 2 (SARS‑CoV‑2) is the virus that causes COVID-19 which is responsible for respiratory illness infection in humans. The virus was first identified in China in 2019 and later spread to other countries worldwide. This study aims to identify the bioactive compounds from mangosteen (&lt;em&gt;Garcinia mangostana &lt;/em&gt;L.) as an antiviral agent via dual inhibitor mechanisms against two SARS-CoV-2 proteases through the &lt;em&gt;in silico &lt;/em&gt;approach. The three-dimensional structure of various bioactive compounds of mangosteen from the database was examined. Furthermore, all the target compounds were analyzed for drug, antiviral activity prediction, virtual screening, molecular interactions, and threedimensional structure visualization. It aimed to determine the potential of the bioactive compounds from mangosteen that can serve as antiviral agents to fight SARS-CoV-2. Results showed that the bioactive compounds from mangosteen have the prospective to provide antiviral agents that contradict the virus via dual inhibitory mechanisms. In summary, the binding of the various bioactive compounds from mangosteen results in low binding energy and is expected to have the ability to induce any activity of the target protein binding reaction. Therefore, it allows various bioactive compounds from mangosteen to act as dual inhibitory mechanisms for COVID-19 infection.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Antiviral agent, COVID-19, &lt;em&gt;Garcinia mangostana&lt;/em&gt; L., In silico approach, SARS-CoV-2.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">85</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;ANM Ansori&lt;sup&gt;1&lt;/sup&gt;, VD Kharisma&lt;sup&gt;2&lt;/sup&gt;, AA Parikesit&lt;sup&gt;3&lt;/sup&gt;, FA Dian&lt;sup&gt;4&lt;/sup&gt;, RT Probojati&lt;sup&gt;5&lt;/sup&gt;, M Rebezov&lt;sup&gt;6,7&lt;/sup&gt;, P Scherbakov&lt;sup&gt;8&lt;/sup&gt;, P Burkov&lt;sup&gt;9&lt;/sup&gt;, G Zhdanova7, A Mikhalev&lt;sup&gt;7&lt;/sup&gt;, Y Antonius&lt;sup&gt;10&lt;/sup&gt;, MRF Pratama&lt;sup&gt;11,12&lt;/sup&gt;, NI Sumantri&lt;sup&gt;13&lt;/sup&gt;, TH Sucipto&lt;sup&gt;14&lt;/sup&gt;, R Zainul&lt;sup&gt;15&lt;/sup&gt;,*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctoral Program of Veterinary Science, Faculty of Veterinary Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Master Program of Biology, Department of Biology, Faculty of Mathematics and Natural Sciences, Brawijaya University, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Bioinformatics, School of Life Sciences, Indonesia International Institute for Life Sciences, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biochemistry and Biotechnology, Faculty of Agronomy, Horticulture and Bioengineering, Poznan University of Life Sciences, Poznan, POLAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Faculty of Agriculture, Universitas Kadiri, Kediri, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;K.G. Razumovsky Moscow State University of Technologies and Management (The First Cossack University), Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Department of Infectious Diseases and Veterinary, South Ural State Agrarian University, Troitsk, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Center for Biotechnology of Animal Reproduction, South Ural State Agrarian University, Troitsk, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Faculty of Biotechnology, University of Surabaya, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Doctoral Program of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Department of Pharmacy, Faculty of Health Sciences, Universitas Muhammadiyah Palangkaraya, Palangka Raya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Biomedical Engineering Study Program, Department of Electrical Engineering, Faculty of Engineering, Universitas Indonesia, Depok, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Dengue Study Group, Institute of Tropical Disease, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nur Sofiatul Aini</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Muhammad Hermawan Widyananda</style></author><author><style face="normal" font="default" size="100%">Ahmad Affan Ali Murtadlo</style></author><author><style face="normal" font="default" size="100%">Rasyadan Taufiq Probojati</style></author><author><style face="normal" font="default" size="100%">Dora Dayu Rahma Turista</style></author><author><style face="normal" font="default" size="100%">Muhammad Badrut Tamam</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Dony Novaliendry</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Budhi Oktavia</style></author><author><style face="normal" font="default" size="100%">Muhammad Thoriq Albari</style></author><author><style face="normal" font="default" size="100%">Saddam Al Aziz</style></author><author><style face="normal" font="default" size="100%">Muhammad Raffi Ghifari</style></author><author><style face="normal" font="default" size="100%">Okta Suryani</style></author><author><style face="normal" font="default" size="100%">Putri Azhari</style></author><author><style face="normal" font="default" size="100%">Muhammad Arya Ghifari</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Agariadne Dwinggo Samala</style></author><author><style face="normal" font="default" size="100%">Mirella Fonda Maahury</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bioactive Compounds from Purslane (Portulaca oleracea L.) and Star Anise (Illicium verum Hook) as SARS-CoV-2 Antiviral Agent via Dual Inhibitor Mechanism: In Silico Approach</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antiviral agent</style></keyword><keyword><style  face="normal" font="default" size="100%">Illicium verum Hook</style></keyword><keyword><style  face="normal" font="default" size="100%">in silico</style></keyword><keyword><style  face="normal" font="default" size="100%">Portulaca oleracea L.</style></keyword><keyword><style  face="normal" font="default" size="100%">SARS-CoV-2</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">352-357</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes the COVID-19 pandemic that infects humans and attacks the body's immune system. The purpose of the study was to identify the potential of bioactive compounds in purslane (&lt;em&gt;Portulaca oleracea&lt;/em&gt; L.) and star anise (&lt;em&gt;Illicium verum&lt;/em&gt; Hook) via a dual inhibitor mechanism against SARS-CoV-2 proteases with an&lt;em&gt; in silico &lt;/em&gt;approach. The samples were obtained from PubChem and RSCB PDB. Antivirus probability prediction was performed on PASS Online. Virtual screening was performed with PyRx via molecular docking. Visualization was used by PyMol and Discovery Studio. Compounds with the best antiviral potential are indicated by the low binding affinity value to the target proteins, namely SARS-CoV-2 TMPRSS2 and PLpro. The results showed that purslane luteolin has the best antiviral potential. However, further studies are required to validate this computational prediction.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><accession-num><style face="normal" font="default" size="100%">14</style></accession-num><section><style face="normal" font="default" size="100%">352</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nur Sofiatul Aini&lt;sup&gt;1&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;2&lt;/sup&gt;, Muhammad Hermawan Widyananda&lt;sup&gt;2,3&lt;/sup&gt;, Ahmad Affan Ali Murtadlo&lt;sup&gt;2&lt;/sup&gt;, Rasyadan Taufiq Probojati&lt;sup&gt;2,4&lt;/sup&gt;, Dora Dayu Rahma Turista&lt;sup&gt;5&lt;/sup&gt;, Muhammad Badrut Tamam&lt;sup&gt;6&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;7&lt;/sup&gt;, Dony Novaliendry&lt;sup&gt;8,9&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;8,10&lt;/sup&gt;, Budhi Oktavia&lt;sup&gt;8,11&lt;/sup&gt;, Muhammad Thoriq Albari&lt;sup&gt;8,12&lt;/sup&gt;, Saddam Al Aziz&lt;sup&gt;8,13&lt;/sup&gt;, Muhammad Raffi Ghifari&lt;sup&gt;8,12&lt;/sup&gt;, Okta Suryani&lt;sup&gt;8,11&lt;/sup&gt;, Putri Azhari&lt;sup&gt;8,14&lt;/sup&gt;, Muhammad Arya Ghifari&lt;sup&gt;8,12&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;8,15,&lt;/sup&gt; Agariadne Dwinggo Samala&lt;sup&gt;8,16&lt;/sup&gt;, Mirella Fonda Maahury&lt;sup&gt;17&lt;/sup&gt;, ANM Ansori&lt;sup&gt;18&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;8,11,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Mathematics and Natural Sciences, State University of Surabaya, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Division of Molecular Biology and Genetics, Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences, Brawijaya University, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Faculty of Agriculture, Universitas Kadiri, Kediri, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Biology Education Department, Faculty of Teacher Training and Education, Mulawarman University, Samarinda, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Biology, Faculty of Sciences and Technology, Universitas Muhammadiyah Lamongan, Lamongan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysics Informatics (CAMP-BIOTICS), Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Study Program of Informatics, Faculty of Engineering, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Environmental Science, Postgraduate Programme, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Department of Information Technology, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Department Mathematics Education, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Department of Agricultural Technology, Faculty of Agricultural Technology, Andalas University, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Department of Radiology Engineering, Universitas Awal Bros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;16&lt;/sup&gt;Department Informatics and Computer Engineering Education, Faculty of Engineering, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;17&lt;/sup&gt;Chemistry Department, Faculty Mathematics and Natural Sciences, Universitas Pattimura, Ambon, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;18&lt;/sup&gt;Professor Nidom Foundation, Surabaya, INDONESIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Duaa Adnan Alghafli</style></author><author><style face="normal" font="default" size="100%">Zeneb Ali Albahrani</style></author><author><style face="normal" font="default" size="100%">Fatemah Hussain Alnasser</style></author><author><style face="normal" font="default" size="100%">Aldanah Ibrahim Alnajdi</style></author><author><style face="normal" font="default" size="100%">Gharam Mohammed Alanazi</style></author><author><style face="normal" font="default" size="100%">Hussein Ali Burshed</style></author><author><style face="normal" font="default" size="100%">Marwan Mohamed Alshawush</style></author><author><style face="normal" font="default" size="100%">Hany Ezzat Khalil</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chemical Profiling and In Vitro α-amylase Antidiabetic Assessment of Carissa Macrocarpa Flower Extract Cultivated in Saudi Arabia</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antidiabetic</style></keyword><keyword><style  face="normal" font="default" size="100%">Apocynaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Caffeic acid.</style></keyword><keyword><style  face="normal" font="default" size="100%">Carissa macrocarpa</style></keyword><keyword><style  face="normal" font="default" size="100%">α-amylase inhibitory</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">759-765</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;em&gt;Carissa macrocarpa &lt;/em&gt;is commonly known as Natal plum. Its fruits are palatable and used in manufacture of jams while other parts of the plant are used in traditional medicine to treat various diseases. The main objective of current study was to screen the presence of and isolate the various phytochemicals applying standard procedures and to evaluate the&lt;em&gt; in vitro&lt;/em&gt; antidiabetic activity using α-amylase inhibitory assay. The total methanol extract of flower (TMEF) of &lt;em&gt;Carissa macrocarpa &lt;/em&gt;was subjected to several chromatographic procedures. Results demonstrated that TMEF of &lt;em&gt;Carissa macrocarpa &lt;/em&gt;is characterized by the content of different constituents such as flavonoids, steroids, saponins, tannins and carbohydrates at different levels. Chromatographic isolation led to the isolation of kaempferol-3-O-robinobioside and caffeic acid, which were confirmed via using &lt;sup&gt;1&lt;/sup&gt;H, &lt;sup&gt;13&lt;/sup&gt;C, DEPT, COSY, HMQC and HMBC NMR spectroscopic analyses. TMEF exhibited α-amylase inhibitory activity with IC&lt;sub&gt;50 &lt;/sub&gt;value of 65.4 μg/ml when compared to that of the acarbose (standard) (IC&lt;sub&gt;50&lt;/sub&gt; = 39.6 μg/ml). In conclusion, current investigation endorses the traditional use of &lt;em&gt;Carissa macrocarpa &lt;/em&gt;as antidiabetic herb. Hence, the studied TMEF of &lt;em&gt;Carissa macrocarp&lt;/em&gt;a may have the potential being nutraceuticals products for pharmaceutical applications as antidiabetic herbal remedy.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">759</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Duaa Adnan Alghafli*, Zeneb Ali Albahrani, Fatemah Hussain Alnasser, Aldanah Ibrahim Alnajdi, Gharam Mohammed Alanazi, Hussein Ali Burshed, Marwan Mohamed Alshawush, Hany Ezzat Khalil*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, SAUDI ARABIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Marwan Mohamed Alshawush</style></author><author><style face="normal" font="default" size="100%">Hussein Ali Burshed</style></author><author><style face="normal" font="default" size="100%">Abdullah Jalal Alasoom</style></author><author><style face="normal" font="default" size="100%">Abdullah Abdulhamid Altaweel</style></author><author><style face="normal" font="default" size="100%">Hany Ezzat Khalil</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chemical Profiling, Antioxidant and Lipoxygenase Enzyme Inhibition Activities of Wild Edible Truffle (Terfezia boudieri) from Northern Borders of Saudi Arabia</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">Gallic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Lipoxygenase inhibition</style></keyword><keyword><style  face="normal" font="default" size="100%">Terfezia boudieri</style></keyword><keyword><style  face="normal" font="default" size="100%">Truffle</style></keyword><keyword><style  face="normal" font="default" size="100%">β-sitosterol</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">319-326</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Truffles are natural food product very famous for its health benefits for being significant biosource of essential fatty acids, proteins and other antioxidant and phenolic compounds. The current study was conducted to evaluate the phytochemicals, antioxidant and lipoxygenase inhibition activities of &lt;em&gt;Terfezia boudieri of &lt;/em&gt;Saudi origin. Various phytochemicals were screened applying standard procedures. The total methanol extract (TME) of the truffle was subjected to several chromatographic procedures. The antioxidant activity was evaluated by DPPH antioxidant procedure, comparing results with trolox as standard. Results demonstrated that &lt;em&gt;Terfezia boudieri &lt;/em&gt;chemically characterized by the availability of various constituents such as flavonoids, steroids, saponins, tannins and carbohydrates at different levels. Phytochemical investigation led to the isolation of β-sitosterol and gallic acid that were identified using 1H, &lt;sup&gt;13&lt;/sup&gt;C, DEPT, COSY, HMQC and HMBC NMR spectroscopic data. Results demonstrated high antioxidant activity with IC&lt;sub&gt;50&lt;/sub&gt;: 50.4 μg/ml and 31.4 μg/ml for TME and gallic acid, respectively. TME and gallic acid exhibited lipoxygenase inhibitory activity with IC&lt;sub&gt;50&lt;/sub&gt; values 4.59 and 0.53 μg/ml for TME and gallic acid, respectively. The higher lipoxygenase inhibitory activity was presumably correlated to the high antioxidant activity. In conclusion, current investigation confirms the folklore use of &lt;em&gt;Terfezia boudieri&lt;/em&gt; as&lt;em&gt; &lt;/em&gt;antinflammatory food. Hence, the studied &lt;em&gt;Terfezia boudieri &lt;/em&gt;may have a great potential as antioxidant and antinflammatory functional food and nutraceuticals products for pharmaceutical applications.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><accession-num><style face="normal" font="default" size="100%">10</style></accession-num><section><style face="normal" font="default" size="100%">319</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Marwan Mohamed Alshawush*, Hussein Ali Burshed, Abdullah Jalal Alasoom, Abdullah Abdulhamid Altaweel, Hany Ezzat Khalil*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, SAUDI ARABIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shahad Mohammed Nasser Alqahtani</style></author><author><style face="normal" font="default" size="100%">Dalya Ramzi Alsuliman</style></author><author><style face="normal" font="default" size="100%">Abdullah Jalal Alasoom</style></author><author><style face="normal" font="default" size="100%">Hussein Ali Burshed</style></author><author><style face="normal" font="default" size="100%">Marwan Mohamed Alshawush</style></author><author><style face="normal" font="default" size="100%">Abdullah Abdulhamid Altaweel</style></author><author><style face="normal" font="default" size="100%">Hany Ezzat Khalil</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cichorioside a biocoumarin modulates lipid and glucose storage on 3T3-L1 cell lines: In vitro and in silico approach</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">3T3-L1cell lines</style></keyword><keyword><style  face="normal" font="default" size="100%">Cichorioside</style></keyword><keyword><style  face="normal" font="default" size="100%">Oil red O staining</style></keyword><keyword><style  face="normal" font="default" size="100%">PPARγ</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">933-937</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Natural coumarins are reputed to demonstrate several biological effects to improve adverse health conditions including; obesity. This study was conducted to explore the potential&lt;em&gt; in vitro&lt;/em&gt; lipid and glucose modulatory activity of cichorioside on 3T3-L1 cell lines .&lt;strong&gt; Methods: &lt;/strong&gt;The 3T3-L1 cell lines were cultured and cell viability was assessed. Glucose content in medium of cultured cells was measured. Differentiation of 3T3-L1 cells from pre-adipocytes to adipocytes was evaluated upon addition of cichorioside. Expression of mRNA of the peroxisome proliferator-activated receptor gamma (PPARγ) was estimated. &lt;strong&gt;Results: &lt;/strong&gt;Survival of around 90% of cultured cells was observed at 10μM cichorioside. Cichorioside inhibited glucose uptake from the medium by the 3T3-L1 cell lines. Cichorioside considerably inhibited pre-adipocyte differentiation and the lipid content in intercellular storage. Cichorioside demonstrated an upregulation of the mRNA expression of PPARγ. Moreover, the docking studies supported the results &lt;em&gt;via &lt;/em&gt;the deep interaction of cichorioside with amino acids residue of PPAR-γ. Taken together, these findings are the first report on &lt;em&gt;in vitro&lt;/em&gt; evaluation of cichorioside to modulate the lipid storage and glucose uptake of cultured 3T3-L1 cell lines&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">933</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Shahad Mohammed Nasser Alqahtani*, Dalya Ramzi Alsuliman, Abdullah Jalal Alasoom, Hussein Ali Burshed, Marwan Mohamed Alshawush, Abdullah Abdulhamid Altaweel, Hany Ezzat Khalil*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, SAUDI ARABIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ichwan Baihaki</style></author><author><style face="normal" font="default" size="100%">Beti Ernawati Dewi</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Ahmad Affan Ali Murtadlo</style></author><author><style face="normal" font="default" size="100%">Muhammad Badrut Tamam</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Nunuk Hariani Soekamto</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author><author><style face="normal" font="default" size="100%">Kuswati</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Kawther Ameen Muhammed Saeed Aledresi</style></author><author><style face="normal" font="default" size="100%">Nur Farhana Mohd Yusof</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">Pavel Burkov</style></author><author><style face="normal" font="default" size="100%">Marina Derkho</style></author><author><style face="normal" font="default" size="100%">Pavel Scherbakov</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Muhammad Raffi Ghifari</style></author><author><style face="normal" font="default" size="100%">Asmi Citra Malina AR Tasakka</style></author><author><style face="normal" font="default" size="100%">Tengku Siti Hajar Haryuna</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Correlation of the Presence of Non Structural-1 (NS1) Antigen Dengue Virus with Severity of Dengue Infection</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Dengue virus</style></keyword><keyword><style  face="normal" font="default" size="100%">NS1 antigen</style></keyword><keyword><style  face="normal" font="default" size="100%">Thrombocytopenia</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">813-816</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Dengue is a major public health threat worldwide, affecting approximately 3 billion people. More than 100 countries in the world located in tropical and subtropical areas, there are at least 100 to 400 million people infected with the dengue virus which causes dengue hemorrhagic fever (DHF). Soluble Non Structural Protein (sNS1) DENV is a soluble NS1 protein that is secreted and found in the serum of patients during acute infection. Because of its presence early in infection, sNS1 is used as a diagnostic indicator of acute dengue infection. NS1 can directly activate platelets through TLR4 and can further increase platelet aggregation, endothelial cell adhesion, and phagocytosis by macrophages that can cause thrombocytopenia so that high sNS1 levels are associated with disease severity. From the results of the study showed p &amp;lt;0.05. This indicates that there is a correlation between the presence of NS1 and the severity of dengue infection.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><section><style face="normal" font="default" size="100%">813</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ichwan Baihaki&lt;sup&gt;1&lt;/sup&gt;, Beti Ernawati Dewi&lt;sup&gt;2,3&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;4,5&lt;/sup&gt;, Ahmad Affan Ali Murtadlo&lt;sup&gt;5&lt;/sup&gt;, Muhammad Badrut Tamam&lt;sup&gt;6&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;7&lt;/sup&gt;, Nunuk Hariani Soekamto&lt;sup&gt;8&lt;/sup&gt;, ANM Ansori&lt;sup&gt;9&lt;/sup&gt;, Kuswati&lt;sup&gt;10&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;11&lt;/sup&gt;, Kawther Ameen Muhammed Saeed Aledresi&lt;sup&gt;12&lt;/sup&gt;, Nur Farhana Mohd Yusof&lt;sup&gt;13&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;14&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;15&lt;/sup&gt;,&lt;sup&gt;16,17&lt;/sup&gt;, Pavel Burkov&lt;sup&gt;18&lt;/sup&gt;, Marina Derkho&lt;sup&gt;18&lt;/sup&gt;, Pavel Scherbakov&lt;sup&gt;18&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;19,20,*&lt;/sup&gt;, Muhammad Raffi Ghifari&lt;sup&gt;21&lt;/sup&gt;, Asmi Citra Malina AR Tasakka&lt;sup&gt;22&lt;/sup&gt;, Tengku Siti Hajar Haryuna&lt;sup&gt;23&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Master Programme in Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Microbiology, Faculty of Medicine, Universitas Indonesia-RSUPN Cipto Mangunkusumo, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Infectious Disease and Immunology Cluster, Indonesian Medical Education and Research Institute, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biology, Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Division of Molecular Biology and Genetics, Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Biology, Faculty of Sciences and Technology, Universitas Muhammadiyah Lamongan, Lamongan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Radiology Engineering, Universitas Awal Bros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Chemistry Department, Faculty of Mathematics and Natural Science, Hasanuddin University, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Professor Nidom Foundation, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Biology Education Study Program, Faculty of Teacher Training and Education, Jember University, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Environmental Science, Postgraduate Programme, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Biochemistry Department, Hawler Medical University, Erbil, Arbil Governorate, Iraqi Kurdistan, IRAQ.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;College of Engineering (Chemical), Universiti Teknologi MARA (UiTM), Jalan Purnama, Bandar Seri Alam, Masai, Johor, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;16&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;17&lt;/sup&gt;Department of Scientific Research, Russian State Agrarian University, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;18&lt;/sup&gt;Institute of Veterinary Medicine, South Ural State Agrarian University, Troitsk, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;19&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMP-BIOTICS), Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;20&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;21&lt;/sup&gt;Department of Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;22&lt;/sup&gt;Faculty of Marine Science and Fisheries, Universitas Hasanuddin, Makassar, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;23&lt;/sup&gt;Department of Otorhinolaryngology - Head and Neck Surgery, Faculty of Medicine, Universitas Sumatera Utara, Medan, INDONESIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kumboyono Kumboyono</style></author><author><style face="normal" font="default" size="100%">Indah Nur Chomsy</style></author><author><style face="normal" font="default" size="100%">Fitria Nugraha Aini</style></author><author><style face="normal" font="default" size="100%">Titin Andri Wihastuti</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Correlation Pattern of oxLDL, cortisol, hsCRP, and Adiponectin Levels in Atherosclerosis Risk Population-Based on Framingham Risk Score</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">14-20</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; The central pathology of cardiovascular disease (CVD) is atherosclerosis. Therefore, it is necessary to examine proteins involved in the and CVD disease mechanism to predict the occurrence of cardiovascular disease due to atherosclerosis. &lt;strong&gt;Purpose: &lt;/strong&gt;This study analysed the correlation pattern of hsCRP, oxLDL, cortisol, and adiponectin levels in atherosclerotic risk population based on the Framingham Risk Score (FRS) to determine the risk of atherosclerosis. &lt;strong&gt;Methods&lt;/strong&gt; Participants were selected using the purposive sampling method,158 participants classes were fired into three risk groups according to FRS. Blood samples were collected, a hsCRP, oxLDL, cortisol, and adiponectin levels were measured using Enzyme-linked Immunosorbent Assay (ELISA). &lt;strong&gt;Results and Discussion&lt;/strong&gt;: Using the inner model test result, four significant direct relationships are formed, indicated by p-value&amp;lt; 0.000. It was FRS to oxLDL, cortisol adiponectin, cortisol to oxLDL, and oxLDL to adiponectin. Based on the indirect effect analysis, it is known that the indirect effect of FRS on Adiponectin through the increase in hs-CRP levels (0.211), FRS on Adiponectin increases in OxLDL levels is significant (-0.224). The coefficient of the effect of the FRS on Adiponectin levels through an increase in OxLDL levels is negative, and also FRS on Adiponectin. The indirect effect of FRS on Adiponectin is that the indirect effect and is not significant (4.083) through the increase in cortisol levels. &lt;strong&gt;Conclusion&lt;/strong&gt;: All variables used in this study are correlated with each other. FRS with hsCRP and adiponectin form a relationship that directly affects each other. Meanwhile, FRS affect adiponectin through OxLDL and cortisol.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Adiponectin, Atherosclerosis, Cardiovascular disease, Framingham Risk Factor, hsCRP.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">14</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kumboyono Kumboyono&lt;sup&gt;1&lt;/sup&gt;, Indah Nur Chomsy&lt;sup&gt;2&lt;/sup&gt;, Fitria Nugraha Aini&lt;sup&gt;3&lt;/sup&gt;, Titin Andri Wihastuti&lt;sup&gt;1&lt;/sup&gt;,*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;School of Nursing, Faculty of Medicine, University of Brawijaya, Malang, 65145, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Doctoral Program of Medical Science, Faculty of Medicine, University of Brawijaya, Malang, 65145, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Medicine, University of Islam Malang, Malang, INDONESIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Emranul Kabir</style></author><author><style face="normal" font="default" size="100%">M. R. O. Khan Noyon</style></author><author><style face="normal" font="default" size="100%">Md. Amjad Hossain</style></author><author><style face="normal" font="default" size="100%">Pranta Acharjee</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">DFT and Pharmacokinetic Study of Some Heterocyclic Aspirin Derivatives as The Cyclooxygenase Inhibitors: An In-Silico Approach</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ADMET.</style></keyword><keyword><style  face="normal" font="default" size="100%">Aspirin</style></keyword><keyword><style  face="normal" font="default" size="100%">DFT</style></keyword><keyword><style  face="normal" font="default" size="100%">Heterocyclic compound</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">1005-1021</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Ibuprofen and aspirin are frequently used to relieve inflammation, pain, and fever. These are the two most significant non-steroidal and anti-inflammatory drugs (NSAIDs). They prevent the development of prostaglandin by blockampounds have been assessed by ibuprofen as well as quantum mechanical computations. Density functional theory (DFT) with the B3LYP/6-31G+ basis function has been used to elucidate the thermo-chemical, molecular orbital, and optimum geometrical aspects in the gas phase. Using molecular docking and non-bonding interactions, the binding affinities and behaviors of some heterocyclic aspirin analogs have been studied on human cyclooxygenase (COX-1 as well as COX-2) proteins (6Y3C and 5F19). The chemical stability of all structures is supported by geometry and thermo-chemical findings. In contrast to aspirin and ibuprofen, almost all tested analogs exhibited a substantial binding score to the receptor protein (5F19). The ADMET prediction revealed the enhanced pharmacokinetic properties of some derivatives with less acute oral toxicity. Overall, eight heterocyclic aspirin analogues 2-9 were shown to be more effective in inhibiting Cyclooxygenase-2 (5F19) than Cyclooxygenase-1 (6Y3C), indicating that they may be effective as COX-2-related inflammation therapeutic candidates.&lt;/p&gt;
&lt;quillbot-extension-portal&gt;&lt;/quillbot-extension-portal&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><section><style face="normal" font="default" size="100%">1005</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Emranul Kabir&lt;sup&gt;1, 2,*&lt;/sup&gt;, M. R. O. Khan Noyon&lt;sup&gt;1&lt;/sup&gt;, Md. Amjad Hossain&lt;sup&gt;1&lt;/sup&gt;, Pranta Acharjee&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Science, Department of Chemistry, University of Chittagong, Chittagong, 4331, BANGLADESH.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Electrical and Electronic Engineering, International Islamic University Chittagong, Chittagong, 4318, BANGLADESH.&lt;/p&gt;
&lt;quillbot-extension-portal&gt;&lt;/quillbot-extension-portal&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Etty Hary Kusumastuti</style></author><author><style face="normal" font="default" size="100%">Priangga Adi Wiratama</style></author><author><style face="normal" font="default" size="100%">Grace Ariani</style></author><author><style face="normal" font="default" size="100%">Stephanie Natasha Djuanda</style></author><author><style face="normal" font="default" size="100%">Alphania Rahniayu</style></author><author><style face="normal" font="default" size="100%">Nila Kurniasari</style></author><author><style face="normal" font="default" size="100%">Dyah Fauziah</style></author><author><style face="normal" font="default" size="100%">Anny Setijo Rahaju</style></author><author><style face="normal" font="default" size="100%">Isnin Anang Marhana</style></author><author><style face="normal" font="default" size="100%">Alfian Nur Rosyid</style></author><author><style face="normal" font="default" size="100%">Dwi Wahyu</style></author><author><style face="normal" font="default" size="100%">Gilang Muhammad Setyo Nugroho</style></author><author><style face="normal" font="default" size="100%">Adhitri Anggoro</style></author><author><style face="normal" font="default" size="100%">I Komang Rusgi Yandi</style></author><author><style face="normal" font="default" size="100%">Bambang Pujo Semedi</style></author><author><style face="normal" font="default" size="100%">Jilientasia Godrace Lilihata</style></author><author><style face="normal" font="default" size="100%">Ummi Maimunah</style></author><author><style face="normal" font="default" size="100%">Supriadi</style></author><author><style face="normal" font="default" size="100%">Achmad Lefi</style></author><author><style face="normal" font="default" size="100%">Lalu Galih Pratama Rinjani</style></author><author><style face="normal" font="default" size="100%">Edi Suyanto</style></author><author><style face="normal" font="default" size="100%">Ricardo Ardian Nugraha</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Differences in interleukin-6 and interleukin-17 expression in covid-19 post-mortem lung tissue biopsy compared with noncovid- 19</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biopsy</style></keyword><keyword><style  face="normal" font="default" size="100%">COVID-19</style></keyword><keyword><style  face="normal" font="default" size="100%">IL-17</style></keyword><keyword><style  face="normal" font="default" size="100%">IL-6</style></keyword><keyword><style  face="normal" font="default" size="100%">Post mortem lung tissue.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">887-892</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; COVID-19 has spread rapidly around the world. It is necessary to study lung tissue of postmortem COVID19 patients to determine the molecular alteration particularly the role of IL-6 and IL-17 in causing fatality. &lt;strong&gt;Objective:&lt;/strong&gt; This study aims to determine the differences in the expressions of IL-6 and IL-17 in lung tissue of post-mortem COVID-19 patients compared to non-COVID-19 patients. This study also aimed to analyze the correlation between the expressions of IL-6 and IL-17 in lung tissue of post-mortem COVID-19 patients. Methods: This research is an observational analytic study with crosssectional approach. The samples were 15 paraffin blocks of post-mortem lung tissue biopsy of COVID-19 patients, and 15 paraffin blocks of inflammatory lung tissue biopsy or surgery of non-COVID-19 patients. IL-6 and IL-17 expressions were evaluated by immunohistochemical procedure. &lt;strong&gt;Result: &lt;/strong&gt;There was a significant difference in the expression of IL-6 in the COVID-19 group and the non-COVID-19 group with a p-value = 0.001 (p &amp;lt; 0.05). There was a significant difference in the expression of IL-17 in the COVID-19 group and the non-COVID-19 group with p-value = 0.001 (p &amp;lt; 0.05). There was a significant correlation between the expressions of IL-6 and IL-17 in the COVID-19 group, with the Spearman coefficient value (rs) of 0.548 with p = 0.034 (p &amp;lt; 0.05).&lt;strong&gt; Conclusion:&lt;/strong&gt; There are differences in the expression of IL-6 and IL-17 between COVID-19 and non-COVID-19 lung tissue. There is a significant correlation between the expressions of IL-6 and IL-17 in post-mortem lung tissue of COVID-19 patients.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">887</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Etty Hary Kusumastuti&lt;sup&gt;1,*&lt;/sup&gt;, Priangga Adi Wiratama&lt;sup&gt;1&lt;/sup&gt;, Grace Ariani&lt;sup&gt;1&lt;/sup&gt;, Stephanie Natasha Djuanda&lt;sup&gt;1&lt;/sup&gt;, Alphania Rahniayu&lt;sup&gt;1&lt;/sup&gt;, Nila Kurniasari&lt;sup&gt;1&lt;/sup&gt;, Dyah Fauziah1, Anny Setijo Rahaju&lt;sup&gt;1&lt;/sup&gt;, Isnin Anang Marhana&lt;sup&gt;2&lt;/sup&gt;, Alfian Nur Rosyid&lt;sup&gt;2&lt;/sup&gt;, Dwi Wahyu&lt;sup&gt;2&lt;/sup&gt;, Gilang Muhammad Setyo Nugroho&lt;sup&gt;2&lt;/sup&gt;, Adhitri Anggoro&lt;sup&gt;2&lt;/sup&gt;, I Komang Rusgi Yandi&lt;sup&gt;2&lt;/sup&gt; Bambang Pujo Semedi&lt;sup&gt;3&lt;/sup&gt;, Jilientasia Godrace Lilihata&lt;sup&gt;3&lt;/sup&gt;, Ummi Maimunah&lt;sup&gt;4&lt;/sup&gt;, Supriadi&lt;sup&gt;4&lt;/sup&gt;, Achmad Lefi&lt;sup&gt;5&lt;/sup&gt;, Lalu Galih Pratama Rinjani&lt;sup&gt;5&lt;/sup&gt;, Edi Suyanto&lt;sup&gt;6&lt;/sup&gt;, Ricardo Ardian Nugraha&lt;sup&gt;6&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anatomical Pathology, Faculty of Medicine, Universitas Airlangga – Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pulmonology and Respiratory Medicine, Faculty of Medicine, Universitas Airlangga – Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Anesthesiology and Reanimation, Faculty of Medicine, Universitas Airlangga University – Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Internal Medicine, Faculty of Medicine, Universitas Airlangga – Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Cardiology and Vascular Medicine, Faculty of Medicine, Universitas Airlangga – Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Forensics and Medicolegal Medicine, Faculty of Medicine, Universitas Airlangga – Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Paulus Anthony Halim</style></author><author><style face="normal" font="default" size="100%">Wachid Putranto</style></author><author><style face="normal" font="default" size="100%">Aryo Tedjo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Omega-3 Rich Fish Oil on the Kidney Changes in Mice Induced by Azoxymethane and Dextran Sodium Sulfate</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Azoxymethane</style></keyword><keyword><style  face="normal" font="default" size="100%">Dextran sodium sulfate</style></keyword><keyword><style  face="normal" font="default" size="100%">Fish oil</style></keyword><keyword><style  face="normal" font="default" size="100%">Histopathology</style></keyword><keyword><style  face="normal" font="default" size="100%">Kidney</style></keyword><keyword><style  face="normal" font="default" size="100%">Mice</style></keyword><keyword><style  face="normal" font="default" size="100%">Omega-3</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">259-266</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background&lt;/strong&gt;: The study aimed to investigate the effect of omega-3 rich fish oil to kidney of mice induced by Azoxymethane (AOM) and DSS using histopathology parameters. &lt;strong&gt;Method:&lt;/strong&gt; The experimental mice were induced using 10 mg/kg AOM and 2% DSS for 2 weeks randomly allocated randomly into four groups as follows;&lt;strong&gt; Control Group:&lt;/strong&gt; mice that not received fish oil, Low Dose Group: mice that received 1.5 mg/day fish oil, Medium Dose Group: mice that received 3 mg/day fish oil, and High Dose Group: mice that received 6 mg/day fish oil. The omega-3 rich fish oil was given for 12 weeks. &lt;strong&gt;Result:&lt;/strong&gt; The administration of high dose omega-3 rich fish oil was able to reduced necrosis and inflammation foci compared to the control group (p&amp;lt;0.05). Furthermore, the administration of low, medium, and high dose omega-3 rich fish oil was able to significantly reduced vascular edema and cell degeneration foci (p&amp;lt;0.05). The administration of medium and high dose of omega-3 rich fish oil were able to reduce the amount of fibrosis foci compared to the control group (p&amp;lt;0.05) compared to the control group. &lt;strong&gt;Conclusion: &lt;/strong&gt;The result suggested anti-nephrotoxic effect of omega-3 rich fish oil in mice induced by azoxymethane and DSS.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><accession-num><style face="normal" font="default" size="100%">02</style></accession-num><section><style face="normal" font="default" size="100%">259</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kusmardi Kusmardi&lt;sup&gt;1&lt;/sup&gt;, Paulus Anthony Halim&lt;sup&gt;3&lt;/sup&gt;, Wachid Putranto&lt;sup&gt;4,*&lt;/sup&gt;, Aryo Tedjo&lt;sup&gt;2,5&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anatomic Pathology, Doctoral Programme Study of Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Drug Development Research Cluster, Human Cancer Research Cluster, Indonesia Medical Educational and Research Institute, Jl. Salemba Raya No.6, Jakarta, 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Drug Development Research Cluster, Indonesia Medical Educational and Research Institute, Jl. Salemba Raya No.6, Jakarta 10340, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Medicine, Universitas Indonesia, Jakarta, Jl. Salemba Raya No.6, Jakarta, 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Division of Nephrology, Department of Internal Medicine, Dr. Moewardi General Hospital, Faculty of Medicine, Sebelas Maret University, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Medical Chemistry, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya No.6, Jakarta, 10430, Jakarta, Indonesia, 10430, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Raja Yasmin Khalilah</style></author><author><style face="normal" font="default" size="100%">E Zuraidah</style></author><author><style face="normal" font="default" size="100%">Ari Estuningtyas</style></author><author><style face="normal" font="default" size="100%">Aryo Tedjo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Pomegranate Peel Ethanol Extract to TNF-α Expression of Mice Colonic Epithelial Cells Induced Using Dextran Sodium Sulfate (DSS)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Colonic epithelial cells</style></keyword><keyword><style  face="normal" font="default" size="100%">Dextran sodium sulfate</style></keyword><keyword><style  face="normal" font="default" size="100%">Mice.</style></keyword><keyword><style  face="normal" font="default" size="100%">Pomegranate peel ethanol extract</style></keyword><keyword><style  face="normal" font="default" size="100%">TNF-α</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">480-488</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;The conventional drugs for inflammatory bowel disease (IBD) have many side effects that impact patient’s quality of life, leading to the emergence of alternative therapies such as pomegranate peel ethanol extract (PPE). This study aims to investigate the anti-inflammatory effect of PPE by observing TNF-α expression in mice induced chronic inflammation of the colon using dextran sodium sulfate (DSS). &lt;strong&gt;Methods:&lt;/strong&gt; 28 Swiss Webster mice samples were taken and divided into five groups, the control group (6 mice), the negative control group (5 mice), the group that was given DSS and aspirin (6 mice), the group was given DSS and a high dose of PPE (5 mice), and the group was given DSS and a low dose of PPE (6 mice). In mice, distal colonic tissue was taken and then stained immunohistochemically against TNF-α and observed with light microscopy at 400x magnification, and TNF-α expression was assessed using the H-Score. &lt;strong&gt;Results:&lt;/strong&gt; TNF-α expression was significantly lower in the group given a high dose of PPE than the negative control group (p &amp;lt;0.05), with mean rank scores of 3.00 and 8.00. There was no significant difference between the group given PPE with a high dose and aspirin (p&amp;gt; 0.05). &lt;strong&gt;Conclusion:&lt;/strong&gt; TNF-α expression in colonic epithelial cells of mice given DSS decreased upon treatment of a high dose of PPE, indicating a mechanism of decreasing inflammation. PPE also has the same effect as aspirin in reducing inflammation.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><accession-num><style face="normal" font="default" size="100%">01</style></accession-num><section><style face="normal" font="default" size="100%">480</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kusmardi Kusmardi&lt;sup&gt;1-4, &lt;/sup&gt;Raja Yasmin Khalilah&lt;sup&gt;5&lt;/sup&gt;, E Zuraidah&lt;sup&gt;1,*&lt;/sup&gt;, Ari Estuningtyas&lt;sup&gt;6&lt;/sup&gt;, Aryo Tedjo&lt;sup&gt;2,7&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anatomic Pathology, Faculty of Medicine, Universitas Indonesia, Salemba Raya Street no.6, 10430, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Drug Development Research Cluster, Indonesian Medical Education and Research Institute, Universitas Indonesia, Salemba Raya Street no.6, 10430, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Human Cancer Research Cluster, Indonesian Medical Education and Research Institute, Universitas Indonesia, Salemba Raya Street no.6, 10430, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Doctoral Program for Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Salemba Raya Street no.6, 10430, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Faculty of Medicine, Universitas Indonesia, Salemba Raya Street no.6, 10430, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Pharmacology and Therapeutic, Faculty of Medicine Universitas Indonesia, Salemba Raya Street no.6, 10430, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Medical Chemistry, Faculty of Medicine Universitas Indonesia, Salemba Raya Street no.6, 10430, Jakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Trisnawati Mundijo</style></author><author><style face="normal" font="default" size="100%">Yurnadi Hanafi Midoen</style></author><author><style face="normal" font="default" size="100%">Franciscus D. Suyatna</style></author><author><style face="normal" font="default" size="100%">Agung Eru Wibowo</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Seahorse Extract (Hippocampus comes L.) on Caspase-3 and TUNEL assay in Rats After Depot Medroxyprogesterone Acetate Induction</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Apoptotic</style></keyword><keyword><style  face="normal" font="default" size="100%">Caspase-3</style></keyword><keyword><style  face="normal" font="default" size="100%">DMPA</style></keyword><keyword><style  face="normal" font="default" size="100%">Seahorse</style></keyword><keyword><style  face="normal" font="default" size="100%">TUNEL assay</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">253-258</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Seahorse (&lt;em&gt;Hippocampus spp&lt;/em&gt;) is marine fish and have pharmacological activity, such as an antiinflammatory, antioxidative, antifatigue and improve the fertility. Depot medroxyprogesterone acetate (DMPA) is a contraception drug for male and affect the endocrine system by inhibiting pituitary gonadotropin with reduce testosterone levels in 12 weeks. There are limited studies reported the effects seahorse extract (SE) on Caspase-3 and TUNEL assay in rats induced by DMPA. Thirty &lt;em&gt;Sprague-Dawley &lt;/em&gt;(SD) male rats that were induced by 1.25mg/kgbw DMPA in 0 and 12 weeks. The animals were randomly into five groups, following: aquadest (G1), CMC 1% (G2), SE dose of 150 mg/kgbw (G3), SE dose of 225 mg/kgbw (G4), SE dose of 300 mg/kgbw (G5). The rats were gavage every day from seven until week eighteen. On the last week, we taken the right and left testis to observed the apoptotic on Caspase-3 and TUNEL assay. Apoptotic marker was observed through immunohistochemistry from testicular tissue and analysed with plugin ImageJ IHC profiler, which is H-score as the results. Data were analysed using One-Way ANOVA and Bonferroni’s post hoc tests. The SE decrease the Caspase-3 and TUNEL assay expression in rats induced by DMPA until eighteen weeks, with dose 150 mg/kgbw given the significant difference with p=0.028; &amp;lt;0.05 and p=0.000; &amp;lt;0.01. These results suggest that SE decreased germ cells apoptotic in DMPA induced rats.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><accession-num><style face="normal" font="default" size="100%">01</style></accession-num><section><style face="normal" font="default" size="100%">253</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Trisnawati Mundijo&lt;sup&gt;1,2&lt;/sup&gt;, Yurnadi Hanafi Midoen&lt;sup&gt;3,*&lt;/sup&gt;, Franciscus D. Suyatna&lt;sup&gt;4&lt;/sup&gt;, Agung Eru Wibowo&lt;sup&gt;5&lt;/sup&gt;, Kusmardi Kusmardi,&lt;sup&gt;1,6-8&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctoral Programme Biomedical Science, Faculty of Medicine, Universitas Indonesia, Jakarta, Jl. Salemba Raya No.6, Jakarta, 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medical Biology, Faculty of Medicine, Universitas Muhammadiyah Palembang, Jl. KH Bhalqi No. 13 Ulu, Palembang, 30263, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya No.6, Jakarta, 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacology and Therapeutics, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya No.6, Jakarta, 10430, Indonesia.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;National Research and Innovation Agency, Indonesia, Puspiptek Street, Serpong, 15314, South Tangerang, Banten, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Anatomic Pathology, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya No.6, Jakarta, 10430, Indonesia.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Drug Development Research Cluster, Indonesia Medical Educational and Research Institute, Jl. Salemba Raya No.6, Jakarta 10340, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Human Cancer Research Cluster, Indonesia Medical Educational and Research Institute, Jl. Salemba Raya No.6, Jakarta 10340, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prasetyo Sarwono Putro</style></author><author><style face="normal" font="default" size="100%">Dono Indarto</style></author><author><style face="normal" font="default" size="100%">Bambang Purwanto</style></author><author><style face="normal" font="default" size="100%">Widyastuti Soewondo</style></author><author><style face="normal" font="default" size="100%">Sulistyani Kusumaningrum</style></author><author><style face="normal" font="default" size="100%">Khim Yatul Nguzum</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effects of Leaves Extract of Toddalia aculeata on Body Weight, Body Mass Index, Body Fat Content and Resistive Index in Male Rats with High-Fat Diet</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Body Fat Content</style></keyword><keyword><style  face="normal" font="default" size="100%">Body Mass Index</style></keyword><keyword><style  face="normal" font="default" size="100%">Obesity</style></keyword><keyword><style  face="normal" font="default" size="100%">Resistive Index</style></keyword><keyword><style  face="normal" font="default" size="100%">Toddalia Aculeata Extract.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">771-777</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;&lt;em&gt;Dictamine&lt;/em&gt; is found in the Toddalia aculeata plant and is able to interact with &lt;em&gt;Flavin- Containing Monooxygenase-3 &lt;/em&gt;(FMO3) in silico, which mediates endogenous atherosclerosis formation. Therefore, this study aimed to investigate the effects of&lt;em&gt; T. aculeata&lt;/em&gt; extract (TAE) administration on Body Weight (BW), Body Mass Index (BMI), Body Fat Content (BFC), and Resistive Index (RI) in rats with a high-fat diet. &lt;strong&gt;Methods: &lt;/strong&gt;Forty male Sprague-Dawley rats were randomly divided into the negative control (NC), positive control (PC) + 2.98 μg/kg BW &lt;em&gt;dictamine&lt;/em&gt; and treatment (TAE1-3) + 200, 400, and 800 mg/ kg BW TAE respectively. All rats were given a high-fat diet (HFD) for 28 days. The data were analyzed statistically using one-way ANOVA, repeated-measured ANOVA, and Friedman’s tests with p&amp;lt;0.05. &lt;strong&gt;Results:&lt;/strong&gt; The average of rats’ BW in TAE2 (270±13.78 g) and TAE3 (276.62±40.31 g) was lower than that of the NC (304.12± 4.16 g) but only the TAE2 group was significantly different (p=0.032). Rats in the TAE 1-3 groups had the average BMI (26.03±5.61; 21.84±0.81; 20.78±2.17 g/cm&lt;sup&gt;3&lt;/sup&gt;) significantly lower than the NC (29.61±2.28 g/cm&lt;sup&gt;3&lt;/sup&gt;) and the PC (28.67±1.68 g/cm&lt;sup&gt;3&lt;/sup&gt;) for TAE2 and 3. The same pattern was also observed in BFC. All treatment groups had significantly lower RI compared to the NC group (0.62±0.07 cm).&lt;strong&gt; Conclusion&lt;/strong&gt;: Administration of 400 and 800 mg/kg BW TAE for 28 days decreases BW, BMI, BFC, and RI in rats with a high-fat diet. &lt;em&gt;Dictamine&lt;/em&gt; in the ethanol extract of &lt;em&gt;T. aculeata&lt;/em&gt; leaves might contribute to the reduction of RI in rats with a high-fat diet.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">771</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Prasetyo Sarwono Putro&lt;sup&gt;1,2&lt;/sup&gt;, Dono Indarto&lt;sup&gt;1,3,4,*&lt;/sup&gt;, Bambang Purwanto&lt;sup&gt;1,5&lt;/sup&gt;, Widyastuti Soewondo&lt;sup&gt;2&lt;/sup&gt;, Sulistyani Kusumaningrum&lt;sup&gt;1,2&lt;/sup&gt;, Khim Yatul Nguzum&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctorate Program of Medical Sciences, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Radiology, Dr. Moewardi General Hospital/Faculty of Medicine, Universitas Sebelas Maret, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Physiology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Biomedical Laboratory, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Internal Medicine, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rungtiwa Kanthain</style></author><author><style face="normal" font="default" size="100%">Jirakrit Leelarungrayub</style></author><author><style face="normal" font="default" size="100%">Surinporn Likhitsathian</style></author><author><style face="normal" font="default" size="100%">Surapol Natakankitkul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efficacy of Combined Relaxed Deep-Breathing with Chest Mobilization Exercise and Vernonia cinerea-Hard Candy on Smoking Cessation and Oxidative Stress in Active Teenage Smokers</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">7-day point prevalence abstinence rate</style></keyword><keyword><style  face="normal" font="default" size="100%">Chest mobilization exercise</style></keyword><keyword><style  face="normal" font="default" size="100%">Continuous abstinence rate</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidative stress</style></keyword><keyword><style  face="normal" font="default" size="100%">Relaxation deep-breathing</style></keyword><keyword><style  face="normal" font="default" size="100%">Smoking cessation</style></keyword><keyword><style  face="normal" font="default" size="100%">Vernonia cinerea-hard candy.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">720-727</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Smoking cessation is very important worldwide. Chronic smoking can induce oxidative stress and inflammatory status and induce dangerous diseases such as hypertension and lung cancer. Standardized counseling is an important process in a routine program for smoking cessation. Withdrawal symptoms from smoking cessation are a significant barrier to a successful result, and they can be relieved by relaxed deep-breathing exercise. At present, the Thai herb, &lt;em&gt;Vernonia cinerea &lt;/em&gt;(VC), has been claimed to reduce cigarette smoking because of its antioxidant compounds and nicotine that are modified and used as lozenges, gum, and hard candy. However, its efficacy in smoking cessation has not been confirmed. Furthermore, the efficacy of relaxed deep-breathing (rDB) during the chest mobilization exercise (CME) with VC hard candy on smoking cessation and oxidative stress is unclear. Objective: This study aimed to evaluate the combined effects of rDB/CME and VC-hard candy on smoking cessation and oxidative stress status in active teenage smokers. &lt;strong&gt;Methods&lt;/strong&gt;: Hard candy with honey and VC powder from whole mixed parts of the stem, flowers and leaves was developed industrially under the spray dry technique. Thirty active smokers were randomized into three groups; product group (rDB/CME+ product) (aged 25.0 ± 3.0 years, n = 10), placebo group (rDB/CME + placebo) (aged 26.9 ± 3.7 years, n = 10), and a control group with no product or placebo administered (aged 25.6 ± 2.7 years, n=10). All of the groups received consultation on specific smoking cessation and two weeks of strict observation, which was followed up for 8 weeks. The 7-day point prevalence abstinence rates (7-day PAR) and continuous abstinence rate (CAR) were reported at week 2, 4, 6 and 8. In addition, the oxidative stress status with lipid peroxide and glutathione (GSH) in blood was evaluated before the program and after 2 weeks. &lt;strong&gt;Results: &lt;/strong&gt;The results of 7-day PARs in the control group showed no statistical changes at week 2 (0%), 4 (10%), 6 (20%) and 8 (20%), which was the same in the rDB/CME + placebo group (10%, 20%, 30% and 40%, respectively). Whereas, a significant difference was presented in the rDB/CME+ product group (20%, 60%, 80% and 90% respectively). When comparing between the groups, 7-day PARs at week 2 was not statistically different, but it was in the follow-up period at week 4, 6 and 8. There was no statistical difference at week 4 between the three groups, but there was between the rDB/CME+ product, control and rDB/CME+ placebo groups at week 6 and 8. The results of CAR showed no statistical difference between the control and rDB/CWE+ placebo group in any of the periods. Whereas the rDB/CWE+ product group showed a significant difference after week 4. The CAR was statistically different between the groups after week 6 and 8. At week 6, the CAR of the rDB/CWE+ product group was different to the control group. There was no difference between the control and rDB/CWE+ placebo groups, or between the rDB/CWE+ product and placebo groups. At week 8, the CAR of the rDB/CWE+ product group was different from that of the control, but not from the rDB/CWE+ placebo group. Finally, the GSH level increased significantly in the rDB/CWE + product group when compared to the rDB/CWE+placebo group. Moreover, malondialdehyde (MDA) levels decreased significantly in both the placebo and product groups. In addition, MDA levels showed a significant difference between baseline and after 2 weeks in the rDB/CWE + placebo and product groups&lt;strong&gt;. Conclusion:&lt;/strong&gt; Integrating relaxed-deep breathing with chest mobilization exercise and VC hard candy for 2 weeks can help smoking cessation during consultation, and possibly reduce oxidative stress status among active teenage smokers.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">720</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Rungtiwa Kanthain&lt;sup&gt;1&lt;/sup&gt;, Jirakrit Leelarungrayub&lt;sup&gt;2,*&lt;/sup&gt;, Surinporn Likhitsathian&lt;sup&gt;3&lt;/sup&gt;, Surapol Natakankitkul&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Physical Therapy, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Physical Therapy, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Psychiatry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmaceutical Sciences, Faculty of Pharmacology, Chiang Mai University, Chiang Mai 50200, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wendy Nora Martian</style></author><author><style face="normal" font="default" size="100%">Dini Kesuma</style></author><author><style face="normal" font="default" size="100%">Rima Via Angraini</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fingerprint and Multivariate Analysis of Apium Graveolens L. From Different Geographic with Spectroscopic ATR-FTIR</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Apium graveolens L</style></keyword><keyword><style  face="normal" font="default" size="100%">ATR-FTIR fingerprint area</style></keyword><keyword><style  face="normal" font="default" size="100%">Multivariate analysis.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">1022-1028</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background&lt;/strong&gt;: &lt;em&gt;Apium graveolens&lt;/em&gt; L. or widely known as celery is a plant that comes from the Apiaceae family. &lt;em&gt;Apium graveolens &lt;/em&gt;L. is found in the Indonesian Herbal Pharmacopoeia as a nutritious plant. Plants that spread throughout Indonesia, both highlands and lowlands, contain 3-n-butylphthalide, D-limonene, Linalool, Luteolin, Apigenin and Apiin compounds. Differences in geographical location of growth resulted in differences in the content and concentration of &lt;em&gt;Apium graveolens&lt;/em&gt; L. Aim and Objectives: This study was conducted to determine the differences of &lt;em&gt;Apium graveolen&lt;/em&gt;s L. based on its distribution in Indonesia. Indonesia does not yet have a standard for &lt;em&gt;Apium graveolens&lt;/em&gt; L. &lt;strong&gt;Material and Methods&lt;/strong&gt;: this research uses &lt;em&gt;Apium graveolens &lt;/em&gt;provided by the Center for Research and Development of Traditional Medicinal and Medicinal Plants (B2P2TOOT) Tawangmangu. 10 samples from different regions in Indonesia will be read using the ATR-FTIR instrument in the finger print area as well as PCA (principal principal) multivariate analysis. component analysis) and HCA (Hierarchical Clustering Analysis). &lt;strong&gt;Results: &lt;/strong&gt;The PCA results show the highest number of variants on PC 1 91,98% and PC 2 variants at 4,71%. In the quadrant 4 score plot, it was found that there was a closeness between the standard sample and the S2 sample (Materia Medika Batu). &lt;strong&gt;Conclusion: &lt;/strong&gt;The result of this study is that there is a mutually supportive relationship from spectrum readings, sample location (temperature, soil moisture content, height (m a.s.l) with multivariate analysis (PCA, HCA results) when compared to the geographic location of each sample.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><section><style face="normal" font="default" size="100%">1022</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Wendy Nora Martian&lt;sup&gt;1&lt;/sup&gt;, Dini Kesuma&lt;sup&gt;2,*&lt;/sup&gt;, Rima Via Angraini&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Master of Industrial Pharmacy, Faculty of Pharmacy, University of Surabaya, Surabaya, East Java 60293, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Surabaya, Surabaya, East Java 60293, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Narasimha Baba Brindavanam</style></author><author><style face="normal" font="default" size="100%">Gurinderjit Singh Goraya</style></author><author><style face="normal" font="default" size="100%">Santosh Pal Singh</style></author><author><style face="normal" font="default" size="100%">Amandeep Kumar</style></author><author><style face="normal" font="default" size="100%">Ankita Tiwari</style></author><author><style face="normal" font="default" size="100%">Badari Narayan Sarvepalli</style></author><author><style face="normal" font="default" size="100%">Pankaj Prasad Raturi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Genetic Diversity in Commiphora wightii (Arn.) Bhandari (Guggul): An Assessment of Populations in Conservation Sites of Kachchh Region (Gujarat) of India</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Gene Pool</style></keyword><keyword><style  face="normal" font="default" size="100%">Guggulu</style></keyword><keyword><style  face="normal" font="default" size="100%">In-situ conservation</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal Plants Conservation Area</style></keyword><keyword><style  face="normal" font="default" size="100%">MPCA</style></keyword><keyword><style  face="normal" font="default" size="100%">UPGMA</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">379-387</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;em&gt; &lt;/em&gt;&lt;/strong&gt;&lt;em&gt;Commiphora wightii&lt;/em&gt; (Arn.) Bhandari (Guggul) is native to semi-arid to arid zones. Its oleoresin gum is used for both medicinal and non-medicinal applications. Reportedly, the species faces high degree conservation threats. A network of Four Medicinal Plants Conservation Areas (MPCA) was carved out in Kachchh region- under financial support from National Medicinal Plants Board. The species also occurs in sanctuary and protected by default. It is considered important to assess genetic diversity of these conserved populations. &lt;strong&gt;Methods:&lt;/strong&gt; A total of 38 accessions of Guggul leaves were collected from five study sites and the whole genomic DNA was extracted for each sample. Genetic study was carried out using ISSR technique. Scorable bands were obtained for 14 out of 40 primers tested. A total of 49 bands were obtained of which 20 were polymorphic in nature. UPGMA dendrograms were constructed for individual sites and also a collective dendrogram for all the study sites.&lt;strong&gt; Results:&lt;/strong&gt; All the 8 accessions of Tharawada MPCA were observed to share a high similarity coefficient. Among rest of three sites, genetic diversity was seen to be narrow. The accessions obtained from NSWS displayed good diversity. These accessions were also noted to be distant to the populations captured in the MPCA sites. &lt;strong&gt;Conclusions&lt;/strong&gt;: Established MPCA sites capture the available gene pool of &lt;em&gt;Commiphora wightii&lt;/em&gt; of Kachchh region. Since NSWS populations are distant to rest of the region, it is suggested to create another site for this purpose. It is desirable to assess the genetic diversity in rest of the MPCA sites.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><accession-num><style face="normal" font="default" size="100%">19</style></accession-num><section><style face="normal" font="default" size="100%">379</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Narasimha Baba Brindavanam&lt;sup&gt;1,*&lt;/sup&gt;, Gurinderjit Singh Goraya&lt;sup&gt;2&lt;/sup&gt;, Santosh Pal Singh&lt;sup&gt;3&lt;/sup&gt;, Amandeep Kumar&lt;sup&gt;4&lt;/sup&gt;, Ankita Tiwari&lt;sup&gt;4&lt;/sup&gt;, Badari Narayan Sarvepalli4, Pankaj Prasad Raturi&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Research Scholar, Amity School of Natural Resources and Sustainable Development, Amity University, Uttar Pradesh, Noida, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;IFS (Retired), (Formerly Principal Chief Conservator of Forests, Government of Himachal Pradesh and Dy. Director General, Indian Council of Forestry Research and Education, Dehradun), INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Director, Amity School of Natural Resources and Sustainable Development, Amity University, Uttar Pradesh, NOIDA (Formerly Principal Chief Conservator of Forests, Government of Assam and Dy. Director General, Indian Council of Forestry Research and Education, Dehradun), INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Bioresources Development Group, Dabur Research and Development Centre, Ghaziabad (UP), INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ermin Rachmawati</style></author><author><style face="normal" font="default" size="100%">M Saifur Rohman</style></author><author><style face="normal" font="default" size="100%">Lintang Widya Sishartami</style></author><author><style face="normal" font="default" size="100%">Djanggan Sargowo</style></author><author><style face="normal" font="default" size="100%">Umi Kalsum</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Silico Modelling, Regulation of Cell Viability and Anti Atherosclerotic Effect in Macrophage by Decaffeinated Coffee and Green Tea Extract</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">46-55</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;The evidence of decaffeinated coffee and green tea extract (DCGTE) in amelioration of atherosclerosis through foam cell formation inhibition has not been established. This study tried to predict the potential role of coffee and tea in foam cell inhibition through&lt;em&gt; in silico&lt;/em&gt; modelling and to investigate the effect of DCGTE on the viability and regulation of foam cell inhibition effect in macrophage cell. &lt;strong&gt;Methods&lt;/strong&gt;: Prediction of physicochemical properties of secondary metabolite of coffee and tea was computed with Swiss ADME. Simulation of molecular docking was performed using PyRx Autodock Vina. Prediction of biological activities was done with PASS SERVER and analyzed the suitability with KEGG Pathway: lipid and atherosclerosis. The effect of DGCTE on macrophage viability was assessed with WST-1 assay then synergistic score was calculated with Synergy Finder. The effect of DCGTE in foam cell formation was examined with light microscope after stained with ORO on oxLDL-stimulated Raw264.7. &lt;strong&gt;Results:&lt;/strong&gt; Molecular docking analysis revealed a strong affinity binding between all active compound of tea or coffee with CD36, but not with PPARγ. Except EGCG, the active compound of tea and coffee fulfil the criteria of drug-likeness. The online prediction function demonstrated that secondary metabolites of coffee and tea potentially inhibit foam cell atherosclerosis. No cytotoxicity effect was obtained after the 24 hours treatment of serial dose of DGCTE 10-640 μg/ml (p=0.000). Moreover, the DGCTE (320/320 μg/ml) had a synergistic effect (Loewe score = 17.26417) and significantly reduced the foam cell number in oxLDL-stimulated Raw264.7 compared to control (p=0.000). &lt;strong&gt;Conclusion:&lt;/strong&gt; The DCGTE exhibit potential benefit as candidate agent for the prevention of atherosclerosis-based diseases.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Atherosclerosis, Coffee polyphenol, Foam cells, Molecular docking, Tea flavonoid.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">46</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ermin Rachmawati&lt;sup&gt;1,2,*&lt;/sup&gt;, M Saifur Rohman&lt;sup&gt;3&lt;/sup&gt;, Lintang Widya Sishartami&lt;sup&gt;4&lt;/sup&gt;, Djanggan Sargowo&lt;sup&gt;3&lt;/sup&gt;, Umi Kalsum &lt;sup&gt;5&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctoral Program of Medical Science, Faculty of Medicine, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biomedical Sciences, Faculty of Medicine and Health Sciences UIN Maulana Malik Ibrahim Malang, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Cardiology and Vascular Medicine, Faculty of Medicine, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Master Program in Biomedical Sciences, Faculty of Medicine, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Pharmacology, Faculty of Medicine, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Priscilla Listiyani</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Arif Nur Muhammad Ansori</style></author><author><style face="normal" font="default" size="100%">Muhammad Hermawan Widyananda</style></author><author><style face="normal" font="default" size="100%">Rasyadan Taufiq Probojati</style></author><author><style face="normal" font="default" size="100%">Ahmad Affan Ali Murtadlo</style></author><author><style face="normal" font="default" size="100%">Dora Dayu Rahma Turista</style></author><author><style face="normal" font="default" size="100%">Md. Emdad Ullah</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Silico Phytochemical Compounds Screening of Allium sativum Targeting the Mpro of SARS-CoV-2</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">604-609</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The global pandemic of coronavirus disease is still widely spread across the world causing catastrophic effect in both human life and global economy. By the end of year 2021, it has caused a total of 5.437.636 deaths across the world. Indonesia has rich plant biodiversity including medicinal plants that may be used for combating the virus. One of the commonly used medicinal plants comes from Allium species and it has been proved to have antiviral activity. Conducting an&lt;em&gt; in silico &lt;/em&gt;study, we screened bioactive compounds that came from &lt;em&gt;Allium sativum&lt;/em&gt; to fight against coronavirus through the inhibition of 3CL-Pro, one of the major protease that have an active role for viral replication. Molecular docking of compounds from &lt;em&gt;Allium sativum&lt;/em&gt; to 3CL-Pro resulting in the discovery of 5 compounds that have the best binding affinity to 3CL-Pro, which are squalene, 1,4-dihydro-2,3-benzoxathiin 3-oxide, 1,2,3-propanetriyl ester, trans-13-octadecenoic acid and methyl-11-hexadecenoate with binding affinity of -7, -6.5, -5.9, -5.7 and -5.6 kcal/mol, respectively. It is very likely that these compounds can be candidates for therapeutic agents and these candidates need to be studied further.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><accession-num><style face="normal" font="default" size="100%">18</style></accession-num><section><style face="normal" font="default" size="100%">604</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Priscilla Listiyani&lt;sup&gt;1&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;1&lt;/sup&gt;, Arif Nur Muhammad Ansori&lt;sup&gt;2&lt;/sup&gt;, Muhammad Hermawan Widyananda&lt;sup&gt;1,3&lt;/sup&gt;, Rasyadan Taufiq Probojati&lt;sup&gt;1,4&lt;/sup&gt;, Ahmad Affan Ali Murtadlo&lt;sup&gt;1&lt;/sup&gt;, Dora Dayu Rahma Turista&lt;sup&gt;5&lt;/sup&gt;, Md. Emdad Ullah&lt;sup&gt;6&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;7&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;8,9,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Molecular Biology and Genetics, Genera si Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Professor Nidom Foundation, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Sciences, Brawijaya University, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Faculty of Agriculture, Universitas Kadiri, Kediri, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Biology Education Department, Faculty of Teacher Training and Education, Mulawarman University, Samarinda, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Chemistry, Mississippi State University, Mississippi State, UNITED STATES.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nur Sofiatul Aini</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Muhammad Hermawan Widyananda</style></author><author><style face="normal" font="default" size="100%">Ahmad Affan Ali Murtadlo</style></author><author><style face="normal" font="default" size="100%">Rasyadan Taufiq Probojati</style></author><author><style face="normal" font="default" size="100%">Dora Dayu Rahma Turista</style></author><author><style face="normal" font="default" size="100%">Muhammad Badrut Tamam</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Elsa Yuniarti</style></author><author><style face="normal" font="default" size="100%">Saddam Al Aziz</style></author><author><style face="normal" font="default" size="100%">Muhammad Raffi Ghifari</style></author><author><style face="normal" font="default" size="100%">Muhammad Thoriq Albari</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Muhammad Arya Ghifari</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Budhi Oktavia</style></author><author><style face="normal" font="default" size="100%">Amalia Putri Lubis</style></author><author><style face="normal" font="default" size="100%">Fajriah Azra</style></author><author><style face="normal" font="default" size="100%">Fadhilah Fitri</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Silico Screening of Bioactive Compounds from Garcinia mangostana L. Against SARS-CoV-2 via Tetra Inhibitors</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antiviral agent</style></keyword><keyword><style  face="normal" font="default" size="100%">Garcinia mangostana L.</style></keyword><keyword><style  face="normal" font="default" size="100%">in silico</style></keyword><keyword><style  face="normal" font="default" size="100%">SARS-CoV-2</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">575-579</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The global COVID-19 pandemic caused by SARS-CoV-2 has been the resulted of massive human deaths since early 2020. The purpose of this study was to determine the potential of mangosteen (&lt;em&gt;Garcinia mangostana &lt;/em&gt;L.) as an inhibitor of RBD spike, helicase, Mpro, and RdRp activity of SARS-CoV-2 with an&lt;em&gt; in silico &lt;/em&gt;approach. The samples were obtained from PubChem and RCSB PDB. Analysis of the similarity of the drug was carried out with the Swiss ADME on the basis of Lipinski rule of five. Prediction of antivirus probabilities was carried out using PASS Online. Molecular screening was performed using PyRx through molecular docking. Discovery Studio was used for visualization. The bioactive compounds with the highest antiviral potential were indicated with the lowest binding affinity to the targeted proteins RBD spike, helicase, Mpro, and RdRp of SARS-CoV-2. The results indicated that mangiferin has the greatest potential as a potential antiviral. However, more research is required to validate the results of these computational predictions.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">575</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nur Sofiatul Aini&lt;sup&gt;1&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;2&lt;/sup&gt;, Muhammad Hermawan Widyananda&lt;sup&gt;2,3&lt;/sup&gt;, Ahmad Affan Ali Murtadlo&lt;sup&gt;2&lt;/sup&gt;, Rasyadan Taufiq Probojati&lt;sup&gt;2,4&lt;/sup&gt;, Dora Dayu Rahma Turista&lt;sup&gt;5&lt;/sup&gt;, Muhammad Badrut Tamam&lt;sup&gt;6&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;7&lt;/sup&gt;, Elsa Yuniarti&lt;sup&gt;8,9&lt;/sup&gt;, Saddam Al Aziz&lt;sup&gt;8,10&lt;/sup&gt;, Muhammad Raffi Ghifari&lt;sup&gt;8,11&lt;/sup&gt;, Muhammad Thoriq Albari&lt;sup&gt;8,11&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;8,12&lt;/sup&gt;, Muhammad Arya Ghifari&lt;sup&gt;8,11&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;8,13&lt;/sup&gt;, Budhi Oktavia&lt;sup&gt;8,14&lt;/sup&gt;, Amalia Putri Lubis&lt;sup&gt;8,14&lt;/sup&gt;, Fajriah Azra&lt;sup&gt;8,14&lt;/sup&gt;, Fadhilah Fitri&lt;sup&gt;8,15&lt;/sup&gt;, ANM Ansori&lt;sup&gt;16&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;17,18,19&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;8,14,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Mathematics and Natural Sciences, State University of Surabaya, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Division of Molecular Biology and Genetics, Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences, Brawijaya University, Malang, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Faculty of Agriculture, Universitas Kadiri, Kediri, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Biology Education Department, Faculty of Teacher Training and Education, Mulawarman University, Samarinda, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Biology, Faculty of Sciences and Technology, Universitas Muhammadiyah Lamongan, Lamongan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Department Mathematics Education, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Department of Information Technology, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Environmental Science, Postgraduate Programme, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Department of Radiology Engineering, Universitas Awal Bros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Department of Statistics, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;16&lt;/sup&gt;Professor Nidom Foundation, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;17&lt;/sup&gt;Department of Scientific Research, Russian State Agrarian University - Moscow Timiryazev Agricultural Academy, Moscow, RUSSIAN FEDERATION&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;18&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;19&lt;/sup&gt;Department of Scientific Research, K.G. Razumovsky Moscow State University of Technologies and Management (The First Cossack University), Moscow, RUSSIAN FEDERATION&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nur Sofiatul Aini</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Muhammad Hermawan Widyananda</style></author><author><style face="normal" font="default" size="100%">Ahmad Affan Ali Murtadlo</style></author><author><style face="normal" font="default" size="100%">Rasyadan Taufiq Probojati</style></author><author><style face="normal" font="default" size="100%">Dora Dayu Rahma Turista</style></author><author><style face="normal" font="default" size="100%">Muhammad Badrut Tamam</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Devni Prima Sari</style></author><author><style face="normal" font="default" size="100%">Muhammad Thoriq Albari</style></author><author><style face="normal" font="default" size="100%">Devi Pernamasari</style></author><author><style face="normal" font="default" size="100%">Muhammad Arya Ghifari</style></author><author><style face="normal" font="default" size="100%">Muhammad Raffi Ghifari</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Muhardi</style></author><author><style face="normal" font="default" size="100%">Budhi Oktavia</style></author><author><style face="normal" font="default" size="100%">Trisna Kumala Sari</style></author><author><style face="normal" font="default" size="100%">Titi Sriwahyuni</style></author><author><style face="normal" font="default" size="100%">Putri Azhari</style></author><author><style face="normal" font="default" size="100%">Mirella Fonda Maahury</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Silico Screening of Bioactive Compounds from Syzygium cumini L. and Moringa oleifera L. Against SARS-CoV-2 via Tetra Inhibitors</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antiviral agent</style></keyword><keyword><style  face="normal" font="default" size="100%">in silico</style></keyword><keyword><style  face="normal" font="default" size="100%">Moringa Oleifera L</style></keyword><keyword><style  face="normal" font="default" size="100%">SARS-CoV-2</style></keyword><keyword><style  face="normal" font="default" size="100%">Syzygium cumini L.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">267-272</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The global pandemic of COVID-19 has caused disastrous consequences for both humans and the economy. The purpose of this study was to determine the potential of juwet (&lt;em&gt;Syzygium cumini&lt;/em&gt; L.) and moringa (&lt;em&gt;Moringa oleifera&lt;/em&gt; L.) as inhibitors of RBD spike, helicase, Mpro, and RdRp activity of SARS-CoV-2 with an &lt;em&gt;in-silico &lt;/em&gt;approach. Samples were obtained from PubChem and RSCB PDB databases. The drug similarity analysis was determined using Swiss ADME and the Lipinski rule of five. Prediction of antivirus probabilities is carried out with PASS Online. Molecular screening is performed by molecular docking using PyRx. Visualization was used using PyMol and Discovery Studio. The bioactive compounds with the best antiviral potential had the lowest affinity bonds to the target proteins against RBD spike, helicase, Mpro, and RdRp of SARS-CoV-2. Results show that ellagic acid from java plum and myricetin from moringa have the best potential as potential antivirals. However, more research is required to validate the results of these computational predictions.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><accession-num><style face="normal" font="default" size="100%">03</style></accession-num><section><style face="normal" font="default" size="100%">267</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nur Sofiatul Aini&lt;sup&gt;1&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;2&lt;/sup&gt;, Muhammad Hermawan Widyananda&lt;sup&gt;2,3&lt;/sup&gt;, Ahmad Affan Ali Murtadlo&lt;sup&gt;2&lt;/sup&gt;, Rasyadan Taufiq Probojati&lt;sup&gt;2,4&lt;/sup&gt;, Dora Dayu Rahma Turista&lt;sup&gt;5,&lt;/sup&gt; Muhammad Badrut Tamam&lt;sup&gt;6&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;7&lt;/sup&gt;, Devni Prima Sari&lt;sup&gt;8,9&lt;/sup&gt;, Muhammad Thoriq Albari&lt;sup&gt;8,10&lt;/sup&gt;, Devi Pernamasari&lt;sup&gt;8,11&lt;/sup&gt;, Muhammad Arya Ghifari&lt;sup&gt;8,10&lt;/sup&gt;, Muhammad Raffi Ghifari&lt;sup&gt;8,10&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;8,12&lt;/sup&gt;, Muhardi&lt;sup&gt;8,13&lt;/sup&gt;, Budhi Oktavia&lt;sup&gt;8,14&lt;/sup&gt;, Trisna Kumala Sari&lt;sup&gt;8,14&lt;/sup&gt;, Titi Sriwahyuni&lt;sup&gt;8,15&lt;/sup&gt;, Putri Azhari&lt;sup&gt;8,16&lt;/sup&gt;, Mirella Fonda Maahury&lt;sup&gt;17&lt;/sup&gt;, ANM Ansori&lt;sup&gt;18&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;8,14,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Mathematics and Natural Sciences, State University of Surabaya, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Division of Molecular Biology and Genetics, Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences, Brawijaya University, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Faculty of Agriculture, Universitas Kadiri, Kediri, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Biology Education Department, Faculty of Teacher Training and Education, Mulawarman University, Samarinda, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Biology, Faculty of Sciences and Technology, Universitas Muhammadiyah Lamongan, Lamongan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Department of Mathematics, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Department of Information Technology, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Department of Radiology Engineering, Universitas Awal Bros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Environmental Science, Postgraduate Programme, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;STMIK Universitas Hang Tuah Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Department Electronic Engineering Education, Faculty of Engineering, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;16&lt;/sup&gt;Department of Agricultural Technology, Faculty of Agricultural Technology, Andalas University, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;17&lt;/sup&gt;Chemistry Department, Faculty Mathematics and Natural Sciences, Universitas Pattimura, Ambon, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;18&lt;/sup&gt;Professor Nidom Foundation, Surabaya, Indonesia&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nala Mawaddani</style></author><author><style face="normal" font="default" size="100%">Ekris Sutiyanti</style></author><author><style face="normal" font="default" size="100%">Muhammad Hermawan Widyananda</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Dora Dayu Rahma Turista</style></author><author><style face="normal" font="default" size="100%">Muhammad Badrut Tamam</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Syamsurizal</style></author><author><style face="normal" font="default" size="100%">Bayu Ramadhani Fajri</style></author><author><style face="normal" font="default" size="100%">Muhammad Raffi Ghifari</style></author><author><style face="normal" font="default" size="100%">Muhammad Thoriq Albari</style></author><author><style face="normal" font="default" size="100%">Muhammad Arya Ghifari</style></author><author><style face="normal" font="default" size="100%">Amalia Putri Lubis</style></author><author><style face="normal" font="default" size="100%">Dony Novaliendry</style></author><author><style face="normal" font="default" size="100%">Dwi Hilda Putri</style></author><author><style face="normal" font="default" size="100%">Fadhilah Fitri</style></author><author><style face="normal" font="default" size="100%">Devni Prima Sari</style></author><author><style face="normal" font="default" size="100%">Alexander Patera Nugraha</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Silico Study of Entry Inhibitor from Moringa oleifera Bioactive Compounds against SARS-CoV-2 Infection</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Active site</style></keyword><keyword><style  face="normal" font="default" size="100%">COVID-19</style></keyword><keyword><style  face="normal" font="default" size="100%">Moringa oleifera</style></keyword><keyword><style  face="normal" font="default" size="100%">Mpro</style></keyword><keyword><style  face="normal" font="default" size="100%">RdRp</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">565-574</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The aim of this study is to screen the content of bioactive compounds of &lt;em&gt;Moringa oleifera &lt;/em&gt;and to identify its potential as an antiviral against COVID 19 through an entry inhibitor mechanism using bioinformatics tools. The sample was obtained from PubChem database. Amino acis sequences were obtained from the NCBI. Protein modeling is made through the SWISSMODEL site. The target proteins for this study were SARS-CoV-2 M&lt;sup&gt;pro&lt;/sup&gt; and RdRp. The protein-inhibitory interaction of the drug from &lt;em&gt;M. oleifera&lt;/em&gt; bioactive compounds to SARS-CoV-2 was predicted by molecular docking with PyRx software. The result shows that&lt;em&gt; M. oleifera &lt;/em&gt;was a potential antiviral candidate for SARS-CoV-2 with an entry inhibitor mechanism through a compound, especially quercetin. The RFMS value of both interactions between M&lt;sup&gt;pro &lt;/sup&gt;and quercetion and RdRp with quercetin were not higher than 1.05. This result still needed further research to prove this prediction.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">565</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nala Mawaddani&lt;sup&gt;1&lt;/sup&gt;, Ekris Sutiyanti&lt;sup&gt;2&lt;/sup&gt;, Muhammad Hermawan Widyananda&lt;sup&gt;1&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;3&lt;/sup&gt;, Dora Dayu Rahma Turista&lt;sup&gt;4&lt;/sup&gt;, Muhammad Badrut Tamam&lt;sup&gt;5&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;6&lt;/sup&gt;, Syamsurizal&lt;sup&gt;7,8&lt;/sup&gt;, Bayu Ramadhani Fajri&lt;sup&gt;7,9&lt;/sup&gt;, Muhammad Raffi Ghifari&lt;sup&gt;7,10&lt;/sup&gt;, Muhammad Thoriq Albari&lt;sup&gt;7,10&lt;/sup&gt;, Muhammad Arya Ghifari&lt;sup&gt;7,10&lt;/sup&gt;, Amalia Putri Lubis&lt;sup&gt;7,11&lt;/sup&gt;, Dony Novaliendry&lt;sup&gt;7,12&lt;/sup&gt;, Dwi Hilda Putri&lt;sup&gt;7,8&lt;/sup&gt;, Fadhilah Fitri&lt;sup&gt;7&lt;/sup&gt;,&lt;sup&gt;13&lt;/sup&gt;, Devni Prima Sari&lt;sup&gt;7,14&lt;/sup&gt;, Alexander Patera Nugraha&lt;sup&gt;15&lt;/sup&gt;, ANM Ansori&lt;sup&gt;16&lt;/sup&gt; , Maksim Rebezov&lt;sup&gt;17,18,19&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;7,11,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Tropical Biology, Faculty of Biology, Universitas Gadjah Mada, Yogyakarta, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Division of Molecular Biology and Genetics, Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Biology Education Department, Faculty of Teacher Training and Education, Mulawarman University, Samarinda, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Biology, Faculty of Sciences and Technology, Universitas Muhammadiyah Lamongan, Lamongan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysics Informatics (CAMP-BIOTICS), Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Information Technology, Dapartement of Electronic, Faculty of Engineering, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Department of Information Technology, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Program Study Informatics, Faculty of Engineering, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Department of Statistics, Faculty of Mathematics and Natural Sciences Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Department of Mathematics, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Department of Orthodontics, Faculty of Dental Medicine, Universitas Airlangga, Surabaya, INDONESIA. 16Professor Nidom Foundation, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;17&lt;/sup&gt;Department of Scientific Research, Russian State Agrarian University - Moscow Timiryazev Agricultural Academy, Moscow, RUSSIAN FEDERATION&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;18&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;19&lt;/sup&gt;Department of Scientific Research, K.G. Razumovsky Moscow State University of Technologies and Management (The First Cossack University), Moscow, RUSSIAN FEDERATION&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aldi Tamara Rahman</style></author><author><style face="normal" font="default" size="100%">Rafia</style></author><author><style face="normal" font="default" size="100%">Aiken Jethro</style></author><author><style face="normal" font="default" size="100%">Putra Santoso</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Ahmad Affan Ali Murtadlo</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Nunuk Hariani Soekamto</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author><author><style face="normal" font="default" size="100%">Kuswati</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Kawther Ameen Muhammed Saeed Aledresi</style></author><author><style face="normal" font="default" size="100%">Nur Farhana Mohd Yusof</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Kiran Dobhal</style></author><author><style face="normal" font="default" size="100%">Tarun Parashar</style></author><author><style face="normal" font="default" size="100%">Muhammad Arya Ghifari</style></author><author><style face="normal" font="default" size="100%">Deffi Ayu Puspito Sari</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Silico Study of the Potential of Endemic Sumatra Wild Turmeric Rhizomes (Curcuma Sumatrana: Zingiberaceae) As Anti-Cancer</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anticancer</style></keyword><keyword><style  face="normal" font="default" size="100%">C. sumatrana</style></keyword><keyword><style  face="normal" font="default" size="100%">in silico</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">806-812</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Cancer is one of the diseases that is the highest cause of death in humans. Most human cancer cells are formed as a result of over-expression of anti-apoptotic proteins. Thus, the activation of these proteins can inhibit pro-apoptotic proteins, then apoptosis will be inhibited so that other apoptotic pathways need to be activated to prevent cancer cells from developing. Current cancer treatments, such as chemotherapy using synthetic compounds, have various side effects, so research on natural based therapies can be used as an alternative in cancer treatment. &lt;em&gt;Curcuma sumatrana&lt;/em&gt; is one of the plants of the Zingiberaceae family which is an endemic plant from Sumatra which is found along the Bukit Barisan. The research was carried out in silico by analyzing the potential bioactivity of the compounds, testing the bioavailability, toxicity, and molecular docking of the bioactive compounds from the ethanol extract of the rhizome of&lt;em&gt; C. sumatrana&lt;/em&gt; which had been previously identified through gas chromatography-mass spectroscopy (GCMS) analysis. The results obtained that the compound 9-Acetyl-S-octahydrophenanthrene and 3-Oxoandrosta- 1,4-dien-17.beta.-spiro-2'-3'-oxo-oxetanecontained in &lt;em&gt;C. sumatrana &lt;/em&gt;has the potential to be developed as an anticancer where the compound has good bioavailability value and is not toxic and potentially can trigger apoptosis. However, the results of this study need to be analyzed further with an in vitro or in vivo approach.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><section><style face="normal" font="default" size="100%">806</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Aldi Tamara Rahman&lt;sup&gt;1&lt;/sup&gt;, Rafia&lt;sup&gt;1&lt;/sup&gt;, Aiken Jethro&lt;sup&gt;2&lt;/sup&gt;, Putra Santoso&lt;sup&gt;1&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;3,4&lt;/sup&gt;, Ahmad Affan Ali Murtadlo&lt;sup&gt;4&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;5&lt;/sup&gt;, Nunuk Hariani Soekamto&lt;sup&gt;6&lt;/sup&gt;, ANM Ansori&lt;sup&gt;7&lt;/sup&gt;, Kuswati&lt;sup&gt;8&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;9&lt;/sup&gt;, Kawther Ameen Muhammed Saeed Aledresi&lt;sup&gt;10&lt;/sup&gt;, Nur Farhana Mohd Yusof&lt;sup&gt;11&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;12&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;13,14,15&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;16,17,*&lt;/sup&gt;, Kiran Dobhal&lt;sup&gt;12&lt;/sup&gt;, Tarun Parashar&lt;sup&gt;12&lt;/sup&gt;, Muhammad Arya Ghifari&lt;sup&gt;18&lt;/sup&gt;, Deffi Ayu Puspito Sari&lt;sup&gt;19&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences, Andalas University, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medicine, Faculty of Medicine, Andalas University, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biology, Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Division of Molecular Biology and Genetics, Generasi Biology Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Radiology Engineering, Universitas Awal Bros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Chemistry Department, Faculty of Mathematics and Natural Science, Hasanuddin University, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Professor Nidom Foundation, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Biology Education Study Program, Faculty of Teacher Training and Education, Jember University, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Environmental Science, Postgraduate Programme, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Biochemistry Department, Hawler Medical University, Erbil, Arbil Governorate, Iraqi Kurdistan, IRAQ.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;College of Engineering (Chemical), Universiti Teknologi MARA (UiTM), Jalan Purnama, Bandar Seri Alam, Masai, Johor, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Department of Scientific Research, Russian State Agrarian University, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;16&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, Padang, INDONESIA. &lt;sup&gt;17&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;18&lt;/sup&gt;Department of Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;19&lt;/sup&gt;Environmental Engineering Program Study, Faculty of Engineering and Computer Sciences, Universitas Bakrie, Jakarta, INDONESIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Tarun Parashar</style></author><author><style face="normal" font="default" size="100%">Pallavi Ghildiyal</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author><author><style face="normal" font="default" size="100%">Rajeev Kumar Sharma</style></author><author><style face="normal" font="default" size="100%">N. G. Raghavendra Rao</style></author><author><style face="normal" font="default" size="100%">Kapil Kalra</style></author><author><style face="normal" font="default" size="100%">Nishan Singh</style></author><author><style face="normal" font="default" size="100%">Nidhi Nainwal</style></author><author><style face="normal" font="default" size="100%">Rajeev Kumar Singh</style></author><author><style face="normal" font="default" size="100%">M. P Singh</style></author><author><style face="normal" font="default" size="100%">Vishwadeepak Kimothi</style></author><author><style face="normal" font="default" size="100%">Alok Bhatt</style></author><author><style face="normal" font="default" size="100%">Ashish Dimri</style></author><author><style face="normal" font="default" size="100%">Ravi Kumar</style></author><author><style face="normal" font="default" size="100%">Amit Semwal</style></author><author><style face="normal" font="default" size="100%">Nur Sofiatul Aini</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">An In Silico Study to Explore the Role of EGFR in Ovarian Cancer</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">EGFR</style></keyword><keyword><style  face="normal" font="default" size="100%">In silico study</style></keyword><keyword><style  face="normal" font="default" size="100%">Protein-protein docking</style></keyword><keyword><style  face="normal" font="default" size="100%">Tyrosine kinases</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">817-821</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;EGFR is a tyrosine kinase receptor that has a role in the tumorigenesis of many types of solid tumors. Aberrantly phosphorylated or overexpressed EGFR is associated with cellular proliferation, prevention of apoptosis, activation of invasion and metastasis, and stimulation of tumor-induced neovascularization. EGFR’s hyperactivity has been observed in ovarian cancer. Although conventional chemotherapy and surgery for advanced ovarian cancer have improved over the years, still there is a critical need for the development of molecular targeted therapies. The major challenge for this approach is the complete understanding of the protein structure of this mega receptor. In this study, we explored this receptor using &lt;em&gt;in silico&lt;/em&gt; tools. The protein structure of the EGFR kinase domain (PDB ID: 1M17) and co-crystal containing EGFR and PTP1B kinase domain fragment (PDB ID: 3I7Z) were obtained from the RCSB Protein Data Bank. We performed protein-protein docking using BioLuminate. It was found in this study that the DADEYL segment of EGFR (position 988-993) which includes autophosphorylated tyrosine at position 992, is the segment that is responsible for the overexpression of this receptor in ovarian cancer. There are currently two main classes of clinically-approved drugs which downregulate EGFR activity; tyrosine kinase inhibitors (TKIs) and monoclonal antibodies (Mabs). However, treatment with both type of therapies has been met with shortcomings. Therefore, there is a need for further studies to explore the suitable ligands that can downregulate its activity.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><section><style face="normal" font="default" size="100%">817</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Vikash Jakhmola&lt;sup&gt;1,*&lt;/sup&gt;, Tarun Parashar&lt;sup&gt;1&lt;/sup&gt;, Pallavi Ghildiyal&lt;sup&gt;1&lt;/sup&gt;, ANM Ansori&lt;sup&gt;2&lt;/sup&gt;, Rajeev Kumar Sharma&lt;sup&gt;3&lt;/sup&gt;, N. G. Raghavendra Rao&lt;sup&gt;4&lt;/sup&gt;, Kapil Kalra&lt;sup&gt;5&lt;/sup&gt;, Nishan Singh&lt;sup&gt;6&lt;/sup&gt;, Nidhi Nainwal&lt;sup&gt;1&lt;/sup&gt;, Rajeev Kumar Singh&lt;sup&gt;7&lt;/sup&gt;, M. P Singh&lt;sup&gt;8&lt;/sup&gt;, Vishwadeepak Kimothi&lt;sup&gt;9&lt;/sup&gt;, Alok Bhatt&lt;sup&gt;10&lt;/sup&gt;, Ashish Dimri&lt;sup&gt;11&lt;/sup&gt;, Ravi Kumar&lt;sup&gt;1&lt;/sup&gt;, Amit Semwal&lt;sup&gt;1&lt;/sup&gt;, Nur Sofiatul Aini&lt;sup&gt;12&lt;/sup&gt;, Maksim Rebezov&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;13,14,15&lt;/strong&gt; &lt;/sup&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Professor Nidom Foundation, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;School of Pharmaceutical and population health informatics, DIT University, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Professor, Kiet School Of Pharmacy, Kiet Group Of Institutions. Delhi-Ncr, Meerut Road, Ghaziabad - 201206 Uttar Pradesh, India&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Alpine College of Management and Technology Dehradun, Uttarakhand, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Srajan Institute of Pharmacy, Lakhimpur Kheri, Uttar Pradesh, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Apex Institute of Pharmacy, Samaspur, Chunar, Mirzapur Uttar Pradesh, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;School of Agriculture, Uttaranchal University, Dehradun, Uttarakhand, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Himalayan Institute of Pharmacy and Research Dehradun, Uttarakhand, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;School of Pharmaceutical Sciences, Himgiri Zee University, Dehradun, Uttarakhand, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;GRD(PG) IMT Dehradun, Uttarakhand, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Faculty of Mathematics and Natural Sciences, State University of Surabaya, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Department of Scientific Research, Russian State Agrarian University - Moscow Timiryazev Agricultural Academy, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Department of Scientific Research, K.G. Razumovsky Moscow State University of technologies and management (The First Cossack University), Moscow, RUSSIAN FEDERATION.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Min Rahminiwati</style></author><author><style face="normal" font="default" size="100%">Trivadila</style></author><author><style face="normal" font="default" size="100%">Dyah Iswantini</style></author><author><style face="normal" font="default" size="100%">Hiroshi Takemori</style></author><author><style face="normal" font="default" size="100%">Mamoru Koketsu</style></author><author><style face="normal" font="default" size="100%">Rut Novalia Rahmawati Sianipar</style></author><author><style face="normal" font="default" size="100%">Suminar Setiati Achmadi</style></author><author><style face="normal" font="default" size="100%">Ahmad Sjahriza</style></author><author><style face="normal" font="default" size="100%">Betty Marita Soebrata</style></author><author><style face="normal" font="default" size="100%">Armi Wulanawati</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Indonesian Medicinal Plants with Anti-inflammatory Properties and Potency as Chronic Obstructive Pulmonary Disease (COPD) Herbal Medicine</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory</style></keyword><keyword><style  face="normal" font="default" size="100%">Bioactive compounds</style></keyword><keyword><style  face="normal" font="default" size="100%">Biological activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Chronic obstructive pulmonary disease</style></keyword><keyword><style  face="normal" font="default" size="100%">Indonesian medicinal plants</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">432-444</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Indonesia is a tropical country with mega-biodiversity. Several medicinal plants locally have been recognized for their anti-inflammatory properties and are traditionally used to help treat respiratory diseases. Chronic obstructive pulmonary disease (COPD) is one of the diseases known as the high cause of death globally, and one of the treatment efforts is by using anti-inflammatory drugs. In developing alternative remedies for COPD, this review summarizes the potential of Indonesian medicinal plants and their ingredients known to have an anti-inflammatory activity to develop alternative remedies for COPD. Primarily, we focus on the medicinal plants that have been scientifically proven to pose some biological activities, such as legetan warak (&lt;em&gt;Adenostemma lavenia&lt;/em&gt;), celery &lt;em&gt;(Apium graveolens&lt;/em&gt;),&lt;em&gt; pegagan&lt;/em&gt; (&lt;em&gt;Centella asiatica&lt;/em&gt;),&lt;em&gt; kenikir &lt;/em&gt;(&lt;em&gt;Cosmos caudatus&lt;/em&gt;), and &lt;em&gt;kersen (Muntingia calabura). &lt;/em&gt;This review is expected to provide more information about Indonesian medicinal plants and their potencies to be developed as COPD herbal medicine and, further, as a treatment to help patients suffering from coronavirus disease (COVID-19).&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><accession-num><style face="normal" font="default" size="100%">26</style></accession-num><section><style face="normal" font="default" size="100%">432</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Min Rahminiwati&lt;sup&gt;1,4,*&lt;/sup&gt;, Trivadila&lt;sup&gt;2,4&lt;/sup&gt;, Dyah Iswantini&lt;sup&gt;2,4&lt;/sup&gt;,*, Hiroshi Takemori&lt;sup&gt;3&lt;/sup&gt;, Mamoru Koketsu&lt;sup&gt;3&lt;/sup&gt;, Rut Novalia Rahmawati Sianipar&lt;sup&gt;2&lt;/sup&gt;, Suminar Setiati Achmadi&lt;sup&gt;2,4&lt;/sup&gt;, Ahmad Sjahriza&lt;sup&gt;2&lt;/sup&gt;, Betty Marita Soebrata&lt;sup&gt;2&lt;/sup&gt;, Armi Wulanawati&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anatomy, Physiology, and Pharmacology, Faculty of Veterinary Medicine, IPB University, Bogor 16680, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, IPB University, Bogor 16680, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Chemistry and Biomolecular Science, Faculty of Engineering, Gifu University, 1-1 Yanagido, Gifu 501-1193, JAPAN.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Tropical Biopharmaca Research Center, IPB University, Bogor 16128, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Linda Chularojmontri</style></author><author><style face="normal" font="default" size="100%">Urarat Nanna</style></author><author><style face="normal" font="default" size="100%">Rawiwun Kaewamatawong</style></author><author><style face="normal" font="default" size="100%">Sudarat Homhual</style></author><author><style face="normal" font="default" size="100%">Wanwisa Suwannaloet</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Inhibitory Effect of Carallia Brachiata Extract Through Regulation of Adipogenesis Pathways in 3T3-L1 Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">3T3-L1 adipocytes</style></keyword><keyword><style  face="normal" font="default" size="100%">Adipogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Carallia brachiata</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">655-660</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Pharmacological effects of &lt;em&gt;Carallia brachiata Merr&lt;/em&gt;. has been reported to show antioxidant effects against the development of diabetes. However, the mechanism underlying antiadipogenic activity have not been investigated. &lt;strong&gt;Objective:&lt;/strong&gt; Effect of&lt;em&gt; Carallia brachiata&lt;/em&gt; ethanolic extract was determined on inhibition of adipogenesis in 3T3-L1 adipocytes.&lt;strong&gt; Materials and Methods&lt;/strong&gt;: Adipose tissue development was performed in preadipocyte 3T3-L1 cells culture. &lt;em&gt;Carallia brachiata&lt;/em&gt; leaf (CL) and stem (CS) part were selected for measuring cytotoxicity, accumulation of lipids, and genes involved in adipogenic differentiation. &lt;strong&gt;Results:&lt;/strong&gt; During the adipogenic differentiation, CS down-regulated gene expression of adipogenic transcription factors (PPARγ, C/EBPα, aP2, FAS, LPL and SREBP1c). However, CL only suppressed SREBP1c and aP2 genes. The accumulation of lipids was suppressed by CS, but CL could not show this effect. &lt;strong&gt;Conclusion&lt;/strong&gt;: Our findings suggest that ethanol extract of &lt;em&gt;Carallia brachiata&lt;/em&gt; stem has a better anti-adipogenesis effect than the leaf part by suppressing adipogenesis-related gene expression. Moreover, inhibition of lipid storage could be decreased insulin resistance risk.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">655</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Linda Chularojmontri&lt;sup&gt;1&lt;/sup&gt;, Urarat Nanna&lt;sup&gt;1&lt;/sup&gt;, Rawiwun Kaewamatawong&lt;sup&gt;2&lt;/sup&gt;, Sudarat Homhual&lt;sup&gt;2&lt;/sup&gt;, Wanwisa Suwannaloet&lt;sup&gt;3,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Preclinical Science, Faculty of Medicine, Thammasat University, Pathum Thani 12120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Pharmaceutical Sciences, Ubon Ratchathani University, Ubon Ratchathani, 34190, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;College of Medicine and Public Health, Ubon Ratchathani University, Ubon Ratchathani, 34190, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Abdullah Abdulhamid Altaweel</style></author><author><style face="normal" font="default" size="100%">Abdullah Jalal Alasoom</style></author><author><style face="normal" font="default" size="100%">Hussein Ali Burshed</style></author><author><style face="normal" font="default" size="100%">Marwan Mohamed Alshawush</style></author><author><style face="normal" font="default" size="100%">Hany Ezzat Khalil</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Insight into Screening of Secondary Metabolites, Phenolic and Flavonoid Contents and Antioxidant Activity of Raphanus sativus L. Cultivated in Eastern Province of Saudi Arabia</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">Folin-Ciocalteau</style></keyword><keyword><style  face="normal" font="default" size="100%">Raphanus sativus</style></keyword><keyword><style  face="normal" font="default" size="100%">total flavonoid.</style></keyword><keyword><style  face="normal" font="default" size="100%">total phenolic</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">313-318</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Medicinal plants and vegetables are promising source of antioxidant products. The purpose of this study is to evaluate the phytochemicals and antioxidant activity of leaves and roots of &lt;em&gt;Raphanus sativus &lt;/em&gt;of Saudi origin. Various phytochemicals were screened in n-hexane, chloroform, ethyl acetate and aqueous fractions of leaves and roots of &lt;em&gt;Raphanus sativus &lt;/em&gt;using standard protocols and IR screening method. Total phenolic (TPC) and flavonoid (TFC) contents were assessed by Folin-Ciocalteau and aluminium chloride methods respectively. The antioxidant activity was evaluated by DPPH antioxidant protocol, using trolox as standard. Results demonstrated that &lt;em&gt;Raphanus sativus&lt;/em&gt; chemically characterized by the availability of various constituents such as flavonoids, steroids, saponins, tannins and carbohydrates at different levels in fractions of leaves and roots of&lt;em&gt; Raphanus sativus&lt;/em&gt; and the absence of cardiac glycosides, anthraquinones and alkaloids which was further confirmed using FTIR analysis. TPC was ranged from (8.92±1.01) and (211.80±1.57) mg GAE/g extract and TFC was ranged from (0.036±0.03) and (11.57±0.60) mg QE/g extract for leaves and roots extracts respectively. Due to the high phenolic and flavonoid content in aqueous and ethyl acetate fractions of leaves and roots extracts , results demonstrated high antioxidant activity with IC&lt;sub&gt;50&lt;/sub&gt;: (56.3±1.3) and (69.7±1.8) for aqueous fractions and (47.2±1.5) and (58.7±0.7) for ethyl acetate fractions of leaves and roots extracts respectively Study revealed that ethyl acetate and aqueous fractions of leaves and roots of&lt;em&gt; Raphanus sativus &lt;/em&gt;could develop a potential natural antioxidant herbal remedy. The study recommends future investigation to isolate and identify the bioactive secondary metabolites in &lt;em&gt;Raphanus sativus.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><accession-num><style face="normal" font="default" size="100%">09</style></accession-num><section><style face="normal" font="default" size="100%">313</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Abdullah Abdulhamid Altaweel*, Abdullah Jalal Alasoom, Hussein Ali Burshed, Marwan Mohamed Alshawush, Hany Ezzat Khalil*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, SAUDI ARABIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Taleb Ali Khalid</style></author><author><style face="normal" font="default" size="100%">Aarab Ahmed</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Medicinal Plants Adopted to Treat Children's Diseases by Traditional Pediatrics ''Women Healers'' In The Souss Massa Region (Agadir Idaoutanan, Inzegane Ait Meloul and Chtouka Ait Baha) Morocco</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Children's diseases</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal plants</style></keyword><keyword><style  face="normal" font="default" size="100%">Traditional medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Women healers</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">880-886</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The population of southern Morocco, particularly that of Souss Massa, uses traditional empirical care, several specialties of traditional medicine exist in the region including women healers considered traditional pediatricians, these women used medicinal plants to treat diseases of infants and children. this study was carried out in order to collect information on the therapeutic practices and medicinal plants adopted and used by women healers named locally by &quot;ferraga&quot; or &quot;tachrift&quot; and &quot;tagouramt&quot; in the Souss Massa region (Agadir Idaoutanan, Inzegane Ait Meloul and Chtouka Ait Baha), in order to preserve and protect this invaluable inheritance from loss and overlook.Using questionnaires, a series of surveys were conducted during the years 2018-2019 and 2019-2020, on the one hand, among the population (sample of 279 people) to determine the importance of these women healers in the health sector of the region of these women healers, and on the other hand, a survey was conducted among these women healers to collect the recipes adopted in the treatment of children's diseases. The population that uses traditional medicine frequently resorts frequently to these women healers to treat digestive and respiratory diseases and the incessant crying. The population that uses traditional medicine resorts to these women healers to treat digestive (30% of population) and respiratory diseases and the incessant crying (24% of population). The floristic analysis of the adopted recipes has revealed 56 plant species divided into 35 botanical families. The most used families are Lamiaceae (12,5%) and Apiaceae (10,71%). the leaves constitute the part more used 32.26% followed by the seeds 22.58%, the infusion is the mode of preparation most used by 35% and the dose is generally by pinch, spoonful or by handful These results show that the women healers have a very important place in the health service, especially they have a very interesting knowledge of the treatment of digestive and respiratory disorders and especially of the effects attributed to sorcery. The plants identified in this study could constitute a data base for further research in the field of phytochemistry and pharmacology.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">880</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Taleb Ali Khalid*, Aarab Ahmed&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Biotechnology and Biomolecule Engineering Research Team, Faculty of Science and Technology, University Abdelmalek Essaadi Tangier Morocco, MOROCCO.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Syeftyan Muhammad Ali Hamami</style></author><author><style face="normal" font="default" size="100%">Michelle Fai</style></author><author><style face="normal" font="default" size="100%">Ahmad Fariduddin Aththar</style></author><author><style face="normal" font="default" size="100%">M Nizam Zulfi Zakaria</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Ahmad Affan Ali Murtadlo</style></author><author><style face="normal" font="default" size="100%">Muhammad Badrut Tamam</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Muhammad Hermawan Widyananda</style></author><author><style face="normal" font="default" size="100%">Dora Dayu Rahma Turista</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">Nikolai Maksimiuk</style></author><author><style face="normal" font="default" size="100%">Nataliya Kulmakova</style></author><author><style face="normal" font="default" size="100%">Evgeniya Latynina</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Oski Illiandri</style></author><author><style face="normal" font="default" size="100%">Khoirun Nisyak</style></author><author><style face="normal" font="default" size="100%">Ernarisa Fitri</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nano Transdermal Delivery Potential of Fucoidan from Sargassum sp. (Brown Algae) as Chemoprevention Agent for Breast Cancer Treatment</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anticancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Breast cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Fucoidan</style></keyword><keyword><style  face="normal" font="default" size="100%">Nano transdermal</style></keyword><keyword><style  face="normal" font="default" size="100%">Sargassum sp. .</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">789-795</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Conventional chemotherapy substances are associated with mild to severe side effects that affect both healthy and cancer cells. It is presumed to improve therapeutic efficacy in coexistence reducing chemotherapy’s side effects. Fucoidan is an anticancer bioactive compound derived from &lt;em&gt;Sargassum sp&lt;/em&gt;. that has low cytotoxic activity. The purpose of this study was to explore the effectiveness of anticancer activities of fucoidan from &lt;em&gt;Sargassum sp.&lt;/em&gt; against breast cancer then analyze the suitability of nano transdermal patch of fucoidan and blueprint the long-term research design of nano transdermal patch as a chemoprevention agent in the chemotherapeutic management of breast cancer. This research was performed through a literature study and &lt;em&gt;in silico&lt;/em&gt; study by imposing carbonic anhydrase IX (CA IX) as a marker of hypoxia and metastatic state of cancer cells. The results showed that the fucoidan from &lt;em&gt;Sargassum sp&lt;/em&gt;. effectively induced apoptosis and prevented metastasis of breast cancer cells through the Bcl-2, Bcl-w, and bad pathways. Fucoidan, in addition, was predicted to inhibit CA IX by Glu4 Glu5, Leu7, Pro8, and Asp6 residues. Therefore, the delivery of fucoidan is favored to have a local effect on the site of breast cancer cells by nano transdermal patch preparations using fucoidan nanoparticle polymer. Further nano transdermal patch development as a treatment for breast cancer is suggested through the stages of formulation optimization, optimum formula activity testing, patent filing, and distribution in health services.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><section><style face="normal" font="default" size="100%">789</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Syeftyan Muhammad Ali Hamami&lt;sup&gt;1&lt;/sup&gt;, Michelle Fai&lt;sup&gt;1&lt;/sup&gt;, Ahmad Fariduddin Aththar&lt;sup&gt;1&lt;/sup&gt;, M Nizam Zulfi Zakaria&lt;sup&gt;1&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;2,3&lt;/sup&gt;, Ahmad Affan Ali Murtadlo&lt;sup&gt;3&lt;/sup&gt;, Muhammad Badrut Tamam&lt;sup&gt;4&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;5&lt;/sup&gt;, Muhammad Hermawan Widyananda&lt;sup&gt;1,3,&lt;/sup&gt; Dora Dayu Rahma Turista&lt;sup&gt;6&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;7,8,9&lt;/sup&gt;, Nikolai Maksimiuk&lt;sup&gt;10&lt;/sup&gt;, Nataliya Kulmakova&lt;sup&gt;11&lt;/sup&gt;, Evgeniya Latynina&lt;sup&gt;11&lt;/sup&gt;, ANM Ansori&lt;sup&gt;12&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;13,14,*&lt;/sup&gt;, Riso Sari Mandeli &lt;sup&gt;15&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;16&lt;/sup&gt;, Oski Illiandri&lt;sup&gt;17&lt;/sup&gt;, Khoirun Nisyak&lt;sup&gt;18&lt;/sup&gt;, Ernarisa Fitri&lt;sup&gt;19&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Life Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biology, Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Division of Molecular Biology and Genetics, Generasi Biology Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biology, Faculty of Sciences and Technology, Universitas Muhammadiyah Lamongan, Lamongan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Biology Education, Faculty of Teacher Training and Education, Mulawarman University, Samarinda, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Department of Scientific Research, Russian State Agrarian University Moscow Timiryazev Agricultural Academy, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Institute of Medical Education, Yaroslav-the-Wise Novgorod State University, Velikiy Novgorod, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Department of Veterinary Medicine, Russian State Agrarian University - Moscow Timiryazev Agricultural Academy, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Professor Nidom Foundation, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMP-BIOTICS), Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Environmental Science, Postgraduate Programme, Universitas Negeri Padang, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;16&lt;/sup&gt;Department of Radiology Engineering, Universitas Awal Bros, Pekanbaru, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;17&lt;/sup&gt;Department of Biomedicine, School of Medicine, Lambung Mangkurat University, Banjarmasin, Indonesia&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;18&lt;/sup&gt;Department of Pharmacy, Faculty of Public Health, Universitas Anwar Medika, Sidoarjo, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;19&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Andalas, Padang, INDONESIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Herman</style></author><author><style face="normal" font="default" size="100%">Fajar Prasetya</style></author><author><style face="normal" font="default" size="100%">Supriatno Salam</style></author><author><style face="normal" font="default" size="100%">Hifdzur Rashif Rijai</style></author><author><style face="normal" font="default" size="100%">Hadi Kuncoro</style></author><author><style face="normal" font="default" size="100%">Rolan Rusli</style></author><author><style face="normal" font="default" size="100%">Agung Rahmadani</style></author><author><style face="normal" font="default" size="100%">Hady Anshory Tamhid</style></author><author><style face="normal" font="default" size="100%">Kuswandi</style></author><author><style face="normal" font="default" size="100%">Dewanto Harjunowibowo</style></author><author><style face="normal" font="default" size="100%">Islamudin Ahmad</style></author><author><style face="normal" font="default" size="100%">Laode Rijai</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic Profile of Simplicia and Ethanolic Leaves Extract from Indonesian Piper betle var. nigra</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Black betle</style></keyword><keyword><style  face="normal" font="default" size="100%">Non-specific parameters</style></keyword><keyword><style  face="normal" font="default" size="100%">Piper betle var. nigra</style></keyword><keyword><style  face="normal" font="default" size="100%">Specific parameters</style></keyword><keyword><style  face="normal" font="default" size="100%">standardization</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">610-618</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;em&gt;Piper betle&lt;/em&gt; var. nigra has potency as an herbal medication. Thus it can be used as a source of medicinal raw materials. &lt;em&gt;Piper betle&lt;/em&gt; var. nigra simplicia and extracts must be controlled to obtain unswerving quality and ensure their pharmacological effects by standardizing them through several specific and non-specific parameters. Specific parameters were analyzed organoleptically in the ethanol extract, namely having a thick consistency, brownish-green or blackish-green color, a mild peculiar odor, a bitter, cherish taste, and a slightly spicy flavor. The microscopic simplicia powder profile is as follows: the lower epidermis with idioblasts in oil cells contour and upper epidermis, sclerenchyma, covering hairs, and transport bundles ladder-type thickening, and idioblasts in oil cells contour. Extract content analysis of simplicia and black betle leaves ethanol extract showed water-soluble extract content of 2.77% and 12.45% and ethanolsoluble extract content of 1.38% and 19.1%. Secondary metabolites in the ethanol extract are flavonoids, polyphenols, tannins, saponins, alkaloids, and steroids. The non-specific parameters of the simplicia and extract are as follows; total ash content of 12.1% and 7.43%; acid insoluble ash content of 4.45% and 1.57%; drying shrinkage of 14.5% and 15.85%; total lead (Pb) contamination 47.5 ppm and 1.2 ppm; and the total cadmium (Cd) contamination &amp;lt;0.2 ppm. The total bacterial contamination in the extract was 4.3x105 colonies/g. The total yeast contamination was 8.3x105 colonies/g and volumetric mass density of the water-soluble extract of 0.96 g/mL and the volumetric mass density of the ethanol-soluble extract of 1.01 g/mL.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">610</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Herman&lt;sup&gt;1,2,*&lt;/sup&gt;, Fajar Prasetya&lt;sup&gt;1,2&lt;/sup&gt;, Supriatno Salam&lt;sup&gt;1,2&lt;/sup&gt;, Hifdzur Rashif Rijai&lt;sup&gt;1,2&lt;/sup&gt;, Hadi Kuncoro&lt;sup&gt;1,2&lt;/sup&gt;, Rolan Rusli&lt;sup&gt;1,2&lt;/sup&gt;, Agung Rahmadani&lt;sup&gt;3&lt;/sup&gt;, Hady Anshory Tamhid&lt;sup&gt;4&lt;/sup&gt;, Dewanto Harjunowibowo&lt;sup&gt;5&lt;/sup&gt;, Islamudin Ahmad&lt;sup&gt;1,2&lt;/sup&gt;, Laode Rijai&lt;sup&gt;1,2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Pharmacy, Universitas Mulawarman, Samarinda 75123, Kalimantan Timur, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmaceuticals Research and Development Laboratory of Pharmaca Tropics, Faculty of Pharmacy, Universitas Mulawarman, Samarinda 75123, Kalimantan Timur, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Departement of Chemistry Education, Faculty of Teaching and Education, Mulawarman University, Samarinda 75123, Kalimantan Timur, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Departement of Pharmacy, Faculty of Mathematics and Natural Sciences, Islamic University of Indonesia, Jogjakarta 55584, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Physics Education, Universitas Sebelas Maret, Surakarta, 57126, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Funsho Oyetunde-Joshua</style></author><author><style face="normal" font="default" size="100%">Roshila Moodley</style></author><author><style face="normal" font="default" size="100%">Hafizah Cheniah</style></author><author><style face="normal" font="default" size="100%">Rene Khan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical and Biological Studies of Helichrysum acutatum DC</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Caffeic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Magnetic resonance</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">603-609</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;em&gt;Helichrysum acutatum &lt;/em&gt;from the Asteraceae family is a shrub indigenous to Southern Africa. The plant is used in traditional medicine as an enema for newborn babies. This study aimed to isolate and identify the bioactive constituents from &lt;em&gt;H. acutatum.&lt;/em&gt; In addition, the crude extracts and isolated compounds were tested for their antioxidant, antibacterial and cytotoxic activities. The phytochemical investigation afforded the known compounds stigmasterol, stigmasterol glucoside, and caffeic acid. The antioxidant activity of the ethyl acetate extract showed higher activity compared to other extracts, ascorbic acid and butylated hydroxytoluene. Antibacterial profiling of all the extracts showed no activity against Gram-negative and Gram-positive bacterial strains. The cytotoxic activity of the crude extracts was assayed&lt;em&gt; in vitro&lt;/em&gt; against two human cancer cell lines, liver hepatoblastoma (HepG2) and colorectal adenocarcinoma (Caco-2). The human embryonic kidney cell line (Hek-293) was used as the non-transformed control. The plant extracts showed insufficient antiproliferative or cytotoxic activity to the tumour and regular cell lines tested, which signifies suitable for human consumption. Overall, this plant has better antioxidant activity than other plants in the genus, which needs further exploration.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">603</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Funsho Oyetunde-Joshua&lt;sup&gt;1&lt;/sup&gt;, Roshila Moodley&lt;sup&gt;1,*&lt;/sup&gt;, Hafizah Cheniah&lt;sup&gt;2&lt;/sup&gt;, Rene Khan&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;School of Chemistry and Physics, University of KwaZulu-Natal, Westville Campus, Private Bag X 54001, Durban, 4000, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;School of Life Sciences, University of KwaZulu- Natal, Westville Campus, Private Bag X54001, Durban 4000, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Howard College Campus, Durban 4041, SOUTH AFRICA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Erna Harfiani</style></author><author><style face="normal" font="default" size="100%">Yudhi Nugraha</style></author><author><style face="normal" font="default" size="100%">Citra Ayu Aprilia</style></author><author><style face="normal" font="default" size="100%">Feda Anisah Makkiyah</style></author><author><style face="normal" font="default" size="100%">Ratna Puspita</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Muhammad Hermawan Widyananda</style></author><author><style face="normal" font="default" size="100%">Ahmad Affan Ali Murtadlo</style></author><author><style face="normal" font="default" size="100%">Dora Dayu Rahma Turista</style></author><author><style face="normal" font="default" size="100%">Muhammad Badrut Tamam</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Mirella Fonda Maahury</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Muhammad Arya Ghifari</style></author><author><style face="normal" font="default" size="100%">Muhammad Thoriq Albari</style></author><author><style face="normal" font="default" size="100%">Muhammad Raffi Ghifari</style></author><author><style face="normal" font="default" size="100%">Asmi Citra Malina A. R. Tasakka</style></author><author><style face="normal" font="default" size="100%">Alexander Patera Nugraha</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The phytochemical and pharmacological activity of extract Kirinyuh (Chromolaena odorata L.) leaves: A Review</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Characterization</style></keyword><keyword><style  face="normal" font="default" size="100%">Chromolaena odorata</style></keyword><keyword><style  face="normal" font="default" size="100%">Kirinyuh</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacological activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">580-586</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;em&gt;C. odorata&lt;/em&gt; L. is considered to be a plant weed that is scattered in various climates. As a weed, this plant contains a variety of beneficial secondary metabolites. Several studies have shown the benefits of &lt;em&gt;C. odorata&lt;/em&gt; L. leaf extract. This study reviews the metabolite content and the pharmacological activities of &lt;em&gt;C. odorata&lt;/em&gt; L. leaf extract. A literature search was carried out to obtain various studies related to the use of this plant extract. Secondary metabolites identified in &lt;em&gt;C. odorata&lt;/em&gt; L. are alkaloids, flavonoids, tannins, saponins, and steroids. Several reports have also shown that even though it is considered a weed, &lt;em&gt;C. odorata &lt;/em&gt;L. leaf extract also provides many benefits due to its pharmacological activities. Various pharmacological activities include anti-inflammatory, anti-microbial, antioxidant, antidyslipidemia, hematologic agent, antidiabetic and anti-cataract, analgesic and antipyretic, wound healing, anti-malaria, mosquito larvicidal, antihypercholesterolemia, and antifungal.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">580</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Erna Harfiani&lt;sup&gt;1&lt;/sup&gt;, Yudhi Nugraha&lt;sup&gt;2&lt;/sup&gt;, Citra Ayu Aprilia&lt;sup&gt;1&lt;/sup&gt;, Feda Anisah Makkiyah&lt;sup&gt;3&lt;/sup&gt;, Ratna Puspita&lt;sup&gt;4&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;5&lt;/sup&gt;, Muhammad Hermawan Widyananda&lt;sup&gt;5,6&lt;/sup&gt;, Ahmad Affan Ali Murtadlo&lt;sup&gt;5&lt;/sup&gt;, Dora Dayu Rahma Turista&lt;sup&gt;7&lt;/sup&gt;, Muhammad Badrut Tamam&lt;sup&gt;8&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;9&lt;/sup&gt;, Mirella Fonda Maahury&lt;sup&gt;10&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;11&lt;/sup&gt;, Muhammad Arya Ghifari&lt;sup&gt;12&lt;/sup&gt;, Muhammad Thoriq Albari&lt;sup&gt;12&lt;/sup&gt;, Muhammad Raffi Ghifari&lt;sup&gt;12&lt;/sup&gt;, Asmi Citra Malina A. R. Tasakka&lt;sup&gt;13&lt;/sup&gt;, Alexander Patera Nugraha&lt;sup&gt;14&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;15,16,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology and Pharmacy, Medical Faculty, UPN Veteran Jakarta, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Badan Riset dan Inovasi Nasional, Jakarta, INDONESIA. 3Department of Surgery, Medical Faculty, UPN Veteran Jakarta, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biochemistry, Medical Faculty, UPN Veteran Jakarta, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Division of Molecular Biology and Genetics, Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences, Brawijaya University, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Biology Education Department, Faculty of Teacher Training and Education, Mulawarman University, Samarinda, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Department of Biology, Faculty of Sciences and Technology, Universitas Muhammadiyah Lamongan, Lamongan, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Environmental Science, Postgraduate Programme, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Pattimura, Ambon, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Department of Radiology Engineering, Universitas Awal Bros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Department of Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Faculty of Marine Science and Fisheries, Universitas Hasanuddin, Makassar, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Department of Orthodontics, Faculty of Dental Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;16&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohammed Wasel Matar</style></author><author><style face="normal" font="default" size="100%">Shahad Mohammed Nasser Alqahtani</style></author><author><style face="normal" font="default" size="100%">Duaa Adnan Alghafli</style></author><author><style face="normal" font="default" size="100%">Abdullah Abdulhamid Altaweel</style></author><author><style face="normal" font="default" size="100%">Abdullah Jalal Alasoom</style></author><author><style face="normal" font="default" size="100%">Hussein Ali Burshed</style></author><author><style face="normal" font="default" size="100%">Marwan Mohamed Alshawush</style></author><author><style face="normal" font="default" size="100%">Hany Ezzat Khalil</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Approach Including Total Phenolic and Flavonoid Contents and Evaluation of in vitro ABTS Antioxidant Capacity and Lipoxygenase Inhibition of Anisosciadium lanatum</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ABTS</style></keyword><keyword><style  face="normal" font="default" size="100%">Anisosciadium lanatum</style></keyword><keyword><style  face="normal" font="default" size="100%">Lipoxygenase</style></keyword><keyword><style  face="normal" font="default" size="100%">total flavonoid</style></keyword><keyword><style  face="normal" font="default" size="100%">total phenolic</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">928-932</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;em&gt;Anisosciadium lanatum&lt;/em&gt; Boiss is commonly known in Bedouins as besbas. Traditional, it is palatable plant and used in medicine of livestock to treat skin conditions . The main objective of current approach was to screen the presence of different kind of metabolites applying standard procedures followed by assessment of total phenolic (TPC) and flavonoids (TFC) contents. In addition, the&lt;em&gt; in vitro &lt;/em&gt;ABTS antioxidant and lipoxygenase activities were evaluated. Different organs (leaves, stems and flowers) of &lt;em&gt;Anisosciadium lanatum&lt;/em&gt; were extracted using 70% methanol to yield total methanol extracts of leaves (TML), stems (TMS) and flowers (TMF). Results demonstrated that TML, TMS and TMF are characterized by the content of different constituents such as flavonoids, phenolics/tannins, steroids, saponins, and carbohydrates at different levels. Ethyl acetate (EA) and butanol (BT) fractions of TML and TMS demonstrated the highest percentage of TPC and TFC. The results demonstrated the competence of EA and BT as free radical scavenger fractions compared to other fractions and its opportunity to contain bioactive antioxidant metabolites . TML, TMS and TMF exhibited Lipoxygenase inhibitory activity with IC50 values of 4.88, 5.40 and 6.05 μg/mL, respectively when compared to that of the positive control baicalein (IC50: 0.27 μg /mL). In conclusion, present investigation highlighted the potential of &lt;em&gt;Anisosciadium lanatum&lt;/em&gt; to be promising candidate with activity against wide range of inflammatory-related diseases.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">928</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Mohammed Wasel Matar*, Shahad Mohammed Nasser Alqahtani, Duaa Adnan Alghafli, Abdullah Abdulhamid Altaweel, Abdullah Jalal Alasoom, Hussein Ali Burshed, Marwan Mohamed Alshawush, Hany Ezzat Khalil*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, SAUDI ARABIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veshalini K</style></author><author><style face="normal" font="default" size="100%">Daryl Jesus Arapoc</style></author><author><style face="normal" font="default" size="100%">Zainah Adam</style></author><author><style face="normal" font="default" size="100%">Rosniza Razali</style></author><author><style face="normal" font="default" size="100%">Noor Azuin Suliman</style></author><author><style face="normal" font="default" size="100%">Noor Azlina Abu Bakar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Screening, In vitro Antioxidant Activities and Zebrafish Embryotoxicity of Abelmoschus esculentus Extracts</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Abelmoschus esculentus</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant Capacity</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword><keyword><style  face="normal" font="default" size="100%">Zebrafish embryotoxicity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">690-701</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Abelmoschus esculentus&lt;/em&gt; (L.) Moench (&lt;em&gt;A. esculentus&lt;/em&gt;) commonly known as okra is being used as a medicinal plant traditionally, due to its phytochemical content that exhibits significant biological activities. &lt;strong&gt;Objective: &lt;/strong&gt;The present study was undertaken to determine phytochemicals, antioxidant activity and embryotoxic effects of hexane extract (HE), chloroform extract (CE), methanol extract (ME), and aqueous extract (AE) of &lt;em&gt;A. esculentus &lt;/em&gt;cultivated in Malaysia. &lt;strong&gt;Materials and Methods&lt;/strong&gt;:&lt;em&gt; A. esculentus&lt;/em&gt; extracts were screened for the phytochemicals while&lt;em&gt; in vitro &lt;/em&gt;antioxidant activities were evaluated by performing 1,1-diphenyl-2-picrylhidrazyl (DPPH) assay and reducing power assay. Meanwhile, the embryotoxicity were accessed by exposing zebrafish embryos to the extracts and developmental endpoint recorded with median lethal concentration (LC&lt;sub&gt;50&lt;/sub&gt;)&lt;strong&gt;. Results: &lt;/strong&gt;The phytochemical screening showed the presence of flavonoids, tannins, phenols, saponins, anthraquinones, alkaloids and reducing sugars. The highest phenolic content was obtained in the CE at 143.85 μg (GAE)/mg extract. Whereas the HE depicted the highest flavonoid content at 63.76 μg (QE)/mg extract. At 1000 μg/mL, ME showed the highest free radical scavenging activity at 28.86 % and reducing power at 0.271, in both DPPH and reducing power assay, respectively. While the CE presented a significant embryotoxic effect on zebrafish with the LC&lt;sub&gt;50&lt;/sub&gt; at 236.07 μg/mL. The morphological malformation of embryos, scoliosis and pericardial oedema were observed at 500 μg/mL of HE and ME treatment. &lt;strong&gt;Conclusion:&lt;/strong&gt; As a result, with various ranges of phytochemical compounds, antioxidant capacities and lower toxic effects of&lt;em&gt; A. esculentus &lt;/em&gt;extracts may be efficient in reducing the inflammation precursors that drive chronic inflammatory illnesses.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><accession-num><style face="normal" font="default" size="100%">28</style></accession-num><section><style face="normal" font="default" size="100%">690</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Veshalini K&lt;sup&gt;1,2&lt;/sup&gt;, Daryl Jesus Arapoc&lt;sup&gt;2&lt;/sup&gt;, Zainah Adam2, Rosniza Razali&lt;sup&gt;2&lt;/sup&gt;, Noor Azuin Suliman&lt;sup&gt;1,*&lt;/sup&gt;, Noor Azlina Abu Bakar&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Medicine, Universiti Sultan Zainal Abidin, Medical Campus, 20400 Kuala Terengganu, Terengganu, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Medical Technology Group, Malaysian Nuclear agency, 43000 Kajang, Selangor, MALAYSIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Faratisha IFD</style></author><author><style face="normal" font="default" size="100%">Cahyono AW</style></author><author><style face="normal" font="default" size="100%">Erwan NE</style></author><author><style face="normal" font="default" size="100%">Putri AM</style></author><author><style face="normal" font="default" size="100%">Ariel DG</style></author><author><style face="normal" font="default" size="100%">Yunita KC</style></author><author><style face="normal" font="default" size="100%">Nugraha RYB</style></author><author><style face="normal" font="default" size="100%">Mardhiyyah K</style></author><author><style face="normal" font="default" size="100%">Fitri LE</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Potential Effect of Nigericin from Streptomyces hygroscopicus subsp. Hygroscopicus Against the Syndemic of Malaria and COVID-19 through Molecular Docking Perspective</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">COVID-19</style></keyword><keyword><style  face="normal" font="default" size="100%">Malaria</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword><keyword><style  face="normal" font="default" size="100%">Nigericin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">268-275</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background&lt;/strong&gt;: Malaria is a constantly challenging problem, notably in the Coronavirus Disease-19 (COVID-19) pandemic. The syndemic condition, malaria-COVID-19 co-infections, had been reported. Our previous study successfully revealed several compounds from&lt;em&gt; Streptomyces hygroscopicus s&lt;/em&gt;ubsp. Hygroscopicus, including nigericin that has both antimalarial and antiviral effects. In malaria infection, &lt;em&gt;Plasmodium falciparum &lt;/em&gt;Chloroquine Resistance Transporter (PfCRT) is the potential target for eliminating &lt;em&gt;Plasmodium.&lt;/em&gt; Meanwhile, for SARS-CoV-2 infection, MPro is an essential protein for SARS-CoV-2 survival. This research aims to examine the potential effect of nigericin towards&lt;em&gt; Plasmodium&lt;/em&gt; and SARS-CoV-2 by assessing its molecular interaction with PfCRT and MPro through molecular docking study.&lt;strong&gt; Methods: &lt;/strong&gt;The protein target PfCRT and MPro were obtained from Protein Data Bank. Nigericin and the control ligand (chloroquine and N3) were obtained from PubChem. The pharmacokinetic analysis was done using SwissADME. Specific molecular docking was conducted using PyRx 0.9 and was visualized using LigPlot and PyMOL. &lt;strong&gt;Results:&lt;/strong&gt; Nigericin has a large molecular weight, leading to the non-fulfillment of the Lipinski rule for oral administration. Through molecular docking study, the binding affinity of the Nigericin-PfCRT complex was -8.1 kcal/mol, and Nigericin-MPro was -8.6 kcal/mol. These binding affinities were stronger than the control ligand. The interaction between Nigericin-PfCRT and Nigericin-MPro share a similar pocket-site and amino acid residues as the control ligands. &lt;strong&gt;Conclusion: &lt;/strong&gt;Nigericin has potential antimalarial and anti-coronavirus effects through molecular docking perspective by assessing the binding affinity and similarity of amino acid residues compared to control. Administration of systemic route can be an option in giving nigericin.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">268</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Faratisha IFD&lt;sup&gt;1&lt;/sup&gt;, Cahyono AW&lt;sup&gt;1,2&lt;/sup&gt;, Erwan NE&lt;sup&gt;1,3&lt;/sup&gt;, Putri AM&lt;sup&gt;1,3&lt;/sup&gt;, Ariel DG&lt;sup&gt;1&lt;/sup&gt;, Yunita KC&lt;sup&gt;1&lt;/sup&gt;, Nugraha RYB&lt;sup&gt;1,4&lt;/sup&gt;, Mardhiyyah K&lt;sup&gt;1,2,5&lt;/sup&gt;, Fitri LE&lt;sup&gt;1,4&lt;/sup&gt;,*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Malaria Research Group, Faculty of Medicine, Universitas Brawijaya, Malang 65145, East Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Doctoral Program in Medical Science, Faculty of Medicine, Universitas Brawijaya, Malang 65145, East Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Master Program in Biomedical Science, Faculty of Medicine, Universitas Brawijaya, Malang 65145, East Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Parasitology, Faculty of Medicine, Universitas Brawijaya, 65145 Malang, East Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Biochemistry &amp;amp; Biomolecular, Faculty of Medicine, Universitas Brawijaya, 65145 Malang, East Java, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Noor Ahmed Abed</style></author><author><style face="normal" font="default" size="100%">Musab Mohammed Khalaf</style></author><author><style face="normal" font="default" size="100%">Mohammed Khalid Jamaludeen Alnori</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%"> The Potential Effect of Silymarin Against Paracetamol-Induced Hepatotoxicity in Male Albino Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">APAP</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">NAC</style></keyword><keyword><style  face="normal" font="default" size="100%">Paracetamol</style></keyword><keyword><style  face="normal" font="default" size="100%">Silymarin</style></keyword><keyword><style  face="normal" font="default" size="100%">TNF-α</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">558-564</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background&lt;/strong&gt;: Being the main metabolic organ, liver stays in touch with toxicity of introduced materials including, drugs. Protection is priceless to avoid complication of liver toxicity. &lt;strong&gt;Objectives&lt;/strong&gt;: This research aimed to assess the protective impact of silymarin (SIL) on hepatotoxicity based on acute paracetamol (APAP) intoxication in rats in comparison with N-acetylcysteine (NAC). &lt;strong&gt;Methods: &lt;/strong&gt;To do so serum was collected and the liver was analyzed for histological findings on rat model-paracetamol toxicity whether alone or in combination with SIL or NAC. The scenario was based on either preconditioning with SIL/NAC before induction of toxicity or afterwards. Serum liver function tests, pro-oxidant/antioxidant status, and proinflammatory markers were detected alongside liver histological study. &lt;strong&gt;Results: &lt;/strong&gt;The results showed that liver function indices, oxidative state, and pro-inflammatory parameters were significantly changed, and histopathological alterations were detected in the liver of the intoxicated group. These modifications were inverted in groups treated with either SIL or NAC. The results of the current study suggested that SIL might be employed as a hepatoprotective drug against liver damage induced by APAP because of its ability to reduce lipid peroxidation, improve antioxidant defense status, and have anti-inflammatory effects.&lt;strong&gt; Conclusion:&lt;/strong&gt; These results are equivalent to NAC therapy which is a standard drug against APAPrelated hepatotoxicity.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">558</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Noor Ahmed Abed&lt;sup&gt;1&lt;/sup&gt;, Musab Mohammed Khalaf&lt;sup&gt;1&lt;/sup&gt;, Mohammed Khalid Jamaludeen Alnori&lt;sup&gt;2,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology and Toxicology, College of Pharmacy, University of Mosul, IRAQ.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Clinical Laboratory Sciences, College of Pharmacy, University of Mosul, IRAQ.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yuna Islamiati</style></author><author><style face="normal" font="default" size="100%">Yani Suryani</style></author><author><style face="normal" font="default" size="100%">Ayuni Adawiyah</style></author><author><style face="normal" font="default" size="100%">Opik Taufiqurrohman</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Devi Purnamasari</style></author><author><style face="normal" font="default" size="100%">Nunuk Hariani Soekamto</style></author><author><style face="normal" font="default" size="100%">Anny Setijo Rahaju</style></author><author><style face="normal" font="default" size="100%">Kuswati</style></author><author><style face="normal" font="default" size="100%">Riso Sari Mandeli</style></author><author><style face="normal" font="default" size="100%">Kawther Ameen Muhammed Saeed Aledresi</style></author><author><style face="normal" font="default" size="100%">Nur Farhana Mohd Yusof</style></author><author><style face="normal" font="default" size="100%">Maksim Rebezov</style></author><author><style face="normal" font="default" size="100%">Shimanovskaya Yanina</style></author><author><style face="normal" font="default" size="100%">Belyakova Natalia</style></author><author><style face="normal" font="default" size="100%">Dmitriy Kulikov</style></author><author><style face="normal" font="default" size="100%">Gulnara Mullagulova</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author><author><style face="normal" font="default" size="100%">Muhammad Thoriq Albari</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Potential of Antivirus Compounds in Gletang (Tridax procumbens Linn.) in Inhibiting 3CLpro Receptor of SARS-CoV-2 Virus by In Silico</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">3CLpro receptor</style></keyword><keyword><style  face="normal" font="default" size="100%">Antivirus</style></keyword><keyword><style  face="normal" font="default" size="100%">Gletang</style></keyword><keyword><style  face="normal" font="default" size="100%">In-silico</style></keyword><keyword><style  face="normal" font="default" size="100%">SARS-CoV-2.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">796-805</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;SARS-CoV-2 virus has caused pandemic disease since the end of 2019. Virus transmission occurs through droplet and infects the host's respiratory tract rapidly. Viral propagation occurs through translation process of genome +ssRNA, then it being replicated forming some new body parts of virus and assemblied into virions that ready to infect. During the replication process, the translated viral genome in the form of polyprotein will be cut into smaller components by proteases, which one is 3CLpro. The presence of the 3CLpro receptor is used in drug development through &lt;em&gt;in-silico &lt;/em&gt;molecular docking process to minimize failures before laboratory test. The antivirus compounds that used to inhibit the 3CLpro receptor are from gletang plant (&lt;em&gt;Tridax procumbens&lt;/em&gt; Linn.). This study aim is to determine the value of binding affinity, the interaction between compounds and receptor, and the effect of drug components. The research was conducted by&lt;em&gt; in-silico&lt;/em&gt; through the molecular docking process of 3CLpro receptor and antivirus compounds of gletang (&lt;em&gt;Tridax procumbens&lt;/em&gt; Linn.), including betulinic acid, kaempferol and lignan. The results showed that the binding affinity of betulinic acid was -6.6 kcal/mol, kaempferol was -5.6 kcal/ mol and lignan was -5.4 kcal/mol. The interaction form of compounds and receptor was hydrogen bond, electrostatic, hydrophobic, and van der Waals. Compared to baicalein compound as a positive control with the value of binding affinity was -6.7 kcal/mol and its interaction with 3CLpro receptor, showed betulinic acid, kaempferol and lignan have smaller ability but they have the potential to inhibit the 3CLpro receptor.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><section><style face="normal" font="default" size="100%">796</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Yuna Islamiati&lt;sup&gt;1&lt;/sup&gt;, Yani Suryani&lt;sup&gt;1&lt;/sup&gt;, Ayuni Adawiyah&lt;sup&gt;1&lt;/sup&gt;, Opik Taufiqurrohman&lt;sup&gt;1&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;2,3&lt;/sup&gt;, Devi Purnamasari&lt;sup&gt;4&lt;/sup&gt;, Nunuk Hariani Soekamto&lt;sup&gt;5&lt;/sup&gt;, Anny Setijo Rahaju&lt;sup&gt;6&lt;/sup&gt;, Kuswati&lt;sup&gt;7&lt;/sup&gt;, Riso Sari Mandeli&lt;sup&gt;8&lt;/sup&gt;, Kawther Ameen Muhammed Saeed Aledresi&lt;sup&gt;9&lt;/sup&gt;, Nur Farhana Mohd Yusof&lt;sup&gt;10&lt;/sup&gt;, Maksim Rebezov&lt;sup&gt;11,12,13&lt;/sup&gt;, Shimanovskaya Yanina&lt;sup&gt;14&lt;/sup&gt;, Belyakova Natalia&lt;sup&gt;15&lt;/sup&gt;, Dmitriy Kulikov&lt;sup&gt;15&lt;/sup&gt;, Gulnara Mullagulova&lt;sup&gt;15&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;16,17,*&lt;/sup&gt;, Muhammad Thoriq Albari&lt;sup&gt;18&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biology, Faculty of Science and Technology, UIN Sunan Gunung Djati Bandung, Bandung, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biology, Faculty of Science and Technology, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Division of Molecular Biology and Genetics, Generasi Biology Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Radiology Engineering, Universitas Awal Bros, Pekanbaru, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Science, Hasanuddin University, INDONESIA&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Pathology, Faculty of Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;7&lt;/sup&gt;Biology Education Study Program, Faculty of Teacher Training and Education, Jember University, INDONESIA&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;8&lt;/sup&gt;Environmental Science, Postgraduate Programme, Universitas Negeri Padang, Padang, INDONESIA&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;9&lt;/sup&gt;Biochemistry Department, Hawler Medical University, Erbil, Arbil Governorate, Iraqi Kurdistan, IRAQ.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;10&lt;/sup&gt;College of Engineering (Chemical), Universiti Teknologi MARA (UiTM), Jalan Purnama, Bandar Seri Alam, Masai, Johor, MALAYSIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;11&lt;/sup&gt;Department of Scientific Research, V. M. Gorbatov Federal Research Center for Food Systems, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;12&lt;/sup&gt;Faculty of Biotechnology and Food Engineering, Ural State Agrarian University, Yekaterinburg, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;13&lt;/sup&gt;Department of Scientific Research, Russian State Agrarian University, Moscow, RUSSIAN FEDERATION&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;14&lt;/sup&gt;Russian State Social University, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;15&lt;/sup&gt;K.G. Razumovsky Moscow State University of Technologies and Management (the First Cossack University), Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;16&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMP-BIOTICS), Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;17&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;18&lt;/sup&gt;Department of Informatics Engineering, Faculty of Computer Sciences, Universitas Brawijaya, Malang, INDONESIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yulius Baki Korassa</style></author><author><style face="normal" font="default" size="100%">Nyi Mekar Saptarini</style></author><author><style face="normal" font="default" size="100%">Resmi Mustarichie</style></author><author><style face="normal" font="default" size="100%">Rini Hendriani</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Potential of Moringa (Moringa oleifera Lamk) Seed Oil as Anti- Alopecia</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-alopecia</style></keyword><keyword><style  face="normal" font="default" size="100%">Fatty Acids</style></keyword><keyword><style  face="normal" font="default" size="100%">Moringa Seed Oil</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytosterol</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">379-387</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; This review article aimed to examine the potentiality of moringa seed oil as anti-alopecia. &lt;strong&gt;Method:&lt;/strong&gt; The data was collected by studying national and international journal articles using several search engines, namely Google and Google Scholar websites, Research Gate, Sciencedirect and Scimagojr. The keywords for this article include moringa seed oil, fatty acids, phytosterol, and anti-alopecia.&lt;strong&gt; Results: &lt;/strong&gt;The result was tabulated in a table and described according to the mechanism of action of the active compounds found in moringa seed oil, fatty acids, phytosterol, and anti-alopecia. Moringa seed oil contain the phytosterol compounds (β-sitosterol, ergosterol and campesterol) show the activities that obstruct the formation of the dihydrotestosterone (DHT) compound known to be the cause of alopecia. The fatty acid compounds found in moringa seed oil (lauric acid, linoleic acid, palmitoleic acid, palmitic acid, and oleic acid) reinforce its potential to be an anti-alopecia. &lt;strong&gt;Conclusion&lt;/strong&gt;: The phytosterol and fatty acid compounds supported the growth of hair to be fertile and healthy.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><section><style face="normal" font="default" size="100%">379</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Yulius Baki Korassa&lt;sup&gt;1,2&lt;/sup&gt;, Nyi Mekar Saptarini&lt;sup&gt;1,*&lt;/sup&gt;, Resmi Mustarichie&lt;sup&gt;1&lt;/sup&gt;, Rini Hendriani&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Analysis and Medicinal Chemistry, Faculty of Pharmacy, Universitas Padjadjaran. Jl. Raya Bandung Sumedang, Jatinangor, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacy Study Program, Health Polytechnic of Ministry of Health in Kupang, Jl. Piet A. Tallo, Liliba, Kupang – East Nusa Tenggara, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacology &amp;amp; Clinical Pharmacy, Faculty of Pharmacy, Universitas Padjadjaran. Jl. Raya Bandung Sumedang, Km. 21 Jatinangor 45363&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nur Sofiatul Aini</style></author><author><style face="normal" font="default" size="100%">Arif Nur Muhammad Ansori</style></author><author><style face="normal" font="default" size="100%">Viol Dhea Kharisma</style></author><author><style face="normal" font="default" size="100%">Muhammad Farraz Syadzha</style></author><author><style face="normal" font="default" size="100%">Muhammad Hermawan Widyananda</style></author><author><style face="normal" font="default" size="100%">Ahmad Affan Ali Murtadlo</style></author><author><style face="normal" font="default" size="100%">Rasyadan Taufiq Probojati</style></author><author><style face="normal" font="default" size="100%">Md. Emdad Ullah</style></author><author><style face="normal" font="default" size="100%">Sin War Naw</style></author><author><style face="normal" font="default" size="100%">Vikash Jakhmola</style></author><author><style face="normal" font="default" size="100%">Rahadian Zainul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Potential Roles of Purslane (Portulaca oleracea L.) as Antimetabolic Syndrome: A Review</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Body weight</style></keyword><keyword><style  face="normal" font="default" size="100%">Insulin resistance</style></keyword><keyword><style  face="normal" font="default" size="100%">Metabolic syndrome</style></keyword><keyword><style  face="normal" font="default" size="100%">Obesity.</style></keyword><keyword><style  face="normal" font="default" size="100%">Portulaca oleracea</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">710-714</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The number of cases of obesity and type 2 diabetes mellitus (T2DM) is part of the metabolic syndrome case. Purslane (&lt;em&gt;Portulaca oleracea&lt;/em&gt; L.) is a plant that has been clinically tested and has the potential to prevent and treat metabolic syndrome as well as pathogenic and pathophysiological activities that cause disease. The aim of this study is to discuss and conclude information regarding the activity and use of purslane (&lt;em&gt;P. oleracea&lt;/em&gt;) as an antimetabolic. This review article is based on scientific publications found on Google Scholar and PubMed databases using the keywords of “Portulaca obesity”, “&lt;em&gt;Portulaca &lt;/em&gt;overweight”, “Portulaca dyslipidemia”, and “&lt;em&gt;Portulaca&lt;/em&gt; metabolic syndrome”. This plant acts on numerous pathways in the metabolic syndrome such as reduction of lipids, blood sugar, body weight and total cholesterol. Purslane (&lt;em&gt;P. oleracea&lt;/em&gt;) can be used as a candidate for a new herbal plant as an anti-metabolic syndrome.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><accession-num><style face="normal" font="default" size="100%">30</style></accession-num><section><style face="normal" font="default" size="100%">710</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nur Sofiatul Aini&lt;sup&gt;1&lt;/sup&gt;, Arif Nur Muhammad Ansori&lt;sup&gt;2&lt;/sup&gt;, Viol Dhea Kharisma&lt;sup&gt;3,4&lt;/sup&gt;, Muhammad Farraz Syadzha&lt;sup&gt;4&lt;/sup&gt;, Muhammad Hermawan Widyananda&lt;sup&gt;3,4&lt;/sup&gt;, Ahmad Affan Ali Murtadlo&lt;sup&gt;4&lt;/sup&gt;, Rasyadan Taufiq Probojati&lt;sup&gt;4&lt;/sup&gt;, Md. Emdad Ullah&lt;sup&gt;5&lt;/sup&gt;, Sin War Naw&lt;sup&gt;6&lt;/sup&gt;, Vikash Jakhmola&lt;sup&gt;7&lt;/sup&gt;, Rahadian Zainul&lt;sup&gt;8,9,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Mathematics and Natural Sciences, State University of Surabaya, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Professor Nidom Foundation, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Mathematics and Natural Sciences, Brawijaya University, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Division of Molecular Biology and Genetics, Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Chemistry, Mississippi State University, Mississippi State, UNITED STATES.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Chemistry, Myitkyina University, Myitkyina, MYANMAR.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Deepika NP</style></author><author><style face="normal" font="default" size="100%">Shyamala Baragur</style></author><author><style face="normal" font="default" size="100%">Mudavath Ravi Naik</style></author><author><style face="normal" font="default" size="100%">Shanker Kalakotla</style></author><author><style face="normal" font="default" size="100%">Muhasina KM</style></author><author><style face="normal" font="default" size="100%">Puja Ghosh</style></author><author><style face="normal" font="default" size="100%">Basavan Duraiswamy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Preparation of Karkataka Taila, an Edible crab Rasayana, and assessment of its toxicological effects on SH-SY5Y cell line and on Drosophila melanogaster embryos</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Drosophila melanogaster</style></keyword><keyword><style  face="normal" font="default" size="100%">Rasayana</style></keyword><keyword><style  face="normal" font="default" size="100%">SH-SY5Y</style></keyword><keyword><style  face="normal" font="default" size="100%">Toxicology</style></keyword><keyword><style  face="normal" font="default" size="100%">Virgin coconut oil.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">423-431</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Karkataka Taila (KT) is a virgin coconut oil (VCO) based Rasayana formulation that is enriched with the flesh of freshwater edible crab, &lt;em&gt;Scylla serrata, &lt;/em&gt;used to treat Parkinson’s Disease (PD) or Kampavata by local Ayurveda practitioners of Kerala state. There is no scientific study carried out on its toxicological effects so far. &lt;strong&gt;Objective:&lt;/strong&gt; To understand the ayurvedic preparation method for KT and assessment of the toxicological effects of the KT and VCO on SH-SY5Y cell lines and&lt;em&gt; Drosophila melanogaster&lt;/em&gt; embryos. &lt;strong&gt;Materials and methods: &lt;/strong&gt;The SH-SY5Y cell lines treated with different concentrations of KT and VCO range from 6.25 μg/ml to 100 μg/ml and&lt;em&gt; Drosophila melanogaster &lt;/em&gt;embryos fed with food containing different concentrations of KT and VCO, ranging from 0.005 % to 10 %. &lt;strong&gt;Results&lt;/strong&gt;: KT and VCO did not show any significant cytotoxicity effect on SH-SY5Y cell lines up to a dose concentration of 25 μg. But, at 50 μg and 100 μg concentrations, KT has shown a cytotoxic effect and it was higher than the VCO. The toxicological analysis in &lt;em&gt;Drosophila&lt;/em&gt; has shown that the survival rate of the KT treated group at concentration ranges from 0.005 % to 10 % is significantly decreased from 78.8 % to 27.7 %, compared to the control group, whereas in VCO treated group, at 0.005 % to 10 %, the survival rate has decreased from 76.2 % to 66 %, which is marginally higher than the KT treated group. &lt;strong&gt;Conclusion:&lt;/strong&gt; Our findings revealed that as the concentration of Rasayana in the medium increases, there is a noticeable adverse effect on the percentage viability in SH-SY5Y cell lines and in the number of offspring in &lt;em&gt;Drosophila. &lt;/em&gt;The effect of vehicle, VCO, at the same concentration has shown a protective effect on cell lines and flies. It can be concluded that the toxic effect has been observed only at higher concentrations of KT and at the lower concentration, the toxic effect has been minimal.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><accession-num><style face="normal" font="default" size="100%">25</style></accession-num><section><style face="normal" font="default" size="100%">423</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Deepika NP&lt;sup&gt;1&lt;/sup&gt;, Shyamala Baragur&lt;sup&gt;2&lt;/sup&gt;, Mudavath Ravi Naik&lt;sup&gt;3&lt;/sup&gt;, Shanker Kalakotla&lt;sup&gt;1&lt;/sup&gt;, Muhasina KM&lt;sup&gt;1&lt;/sup&gt;, Puja Ghosh&lt;sup&gt;1&lt;/sup&gt;, Basavan Duraiswamy&lt;sup&gt;*,1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, 643001, The Nilgiris, Tamilnadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Zoology, University of Mysore, Mysore, Karnataka, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacology, JSS College of Pharmacy, JSS Academy of Higher Education and Research, Ooty, 643001, The Nilgiris, Tamilnadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dalya Ramzi Alsuliman</style></author><author><style face="normal" font="default" size="100%">Zainab Mohammed Al Sultan</style></author><author><style face="normal" font="default" size="100%">Maryam Khalil Almajhad</style></author><author><style face="normal" font="default" size="100%">Nour Kamal Alhajri</style></author><author><style face="normal" font="default" size="100%">Abdullah Abdulhamid Altaweel</style></author><author><style face="normal" font="default" size="100%">Abdullah Jalal Alasoom</style></author><author><style face="normal" font="default" size="100%">Hany Ezzat Khalil</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Profound Assessment of Phytochemical, Botanical and Antioxidant Characteristics Including Determination of Total Phenolic and Flavonoid Contents of Stem Bark of Cordia obliqua L.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ABTS.</style></keyword><keyword><style  face="normal" font="default" size="100%">Boraginaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Cordia obliqua</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">Folin-Ciocalteau</style></keyword><keyword><style  face="normal" font="default" size="100%">Total phenolic and flavonoid</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">753-758</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;em&gt;Cordia obliqua i&lt;/em&gt;s known as Bumber. Its fruits and leaves are popularly used because of antioxidant and anti-diabetic activities. The purpose of this study is to evaluate the phytochemicals and antioxidant activity as well as botanical features of stem bark of &lt;em&gt;Cordia obliqua&lt;/em&gt;. Chemical components were preliminary screened in various fractions based on the polarities including; n-hexane, chloroform, ethyl acetate, butanol and aqueous fractions of using standard procedures. Total phenolic (TPC) and flavonoid (TFC) contents were assessed by Folin-Ciocalteau and aluminium chloride methods respectively. The antioxidant activity was evaluated by ABTS antioxidant procedure, using ascorbic acid as standard. Results confirmed that stem bark of&lt;em&gt; Cordia obliqua&lt;/em&gt; chemically is characterized by the presences of flavonoids, alkaloids, steroids, saponins, tannins and carbohydrates at different levels in various fractions and the absence of cardiac glycosides and anthraquinones. Microscopically, the plant is characterized by presence of big Ca oxalate clusters, various types of xylem vessels and big amount of cork cells. TPC was ranged from 13.6±1.4 and 220.5±3.4 mg GAE/g dry plant extract and TFC was ranged from 0.029±0.12and 15.46±0.33 mg QE/g dry plant extract. Due to the high phenolic and flavonoid content in butanol and ethyl acetate fractions; results of antioxidant using ABTS assay showed high antioxidant activity with IC&lt;sub&gt;5&lt;/sub&gt;0 valued 11.84±1.2 μg/ ml for butanol fraction and 14.81±1.1 μg/ml for ethyl acetate fraction. Taken together, the research work demonstrated the potential natural antioxidant value of the waste product stem bark of &lt;em&gt;Cordia obliqua.&lt;/em&gt; The study endorses forthcoming work to isolate and identify the chemical constituents in stem bark of Cordia obliqua.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article </style></work-type><section><style face="normal" font="default" size="100%">753</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Dalya Ramzi Alsuliman*, Zainab Mohammed Al Sultan, Maryam Khalil Almajhad, Nour Kamal Alhajri, Abdullah Abdulhamid Altaweel, Abdullah Jalal Alasoom, Hany Ezzat Khalil*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982, SAUDI ARABIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Angelina V. Strelyaeva</style></author><author><style face="normal" font="default" size="100%">Anna G. Kharitonova</style></author><author><style face="normal" font="default" size="100%">Larisa B. Vaskova</style></author><author><style face="normal" font="default" size="100%">Alexander N. Luferov</style></author><author><style face="normal" font="default" size="100%">Dmitry O. Bokov</style></author><author><style face="normal" font="default" size="100%">Alina A. Bondar</style></author><author><style face="normal" font="default" size="100%">Natalia V. Bobkova</style></author><author><style face="normal" font="default" size="100%">Nevena Jeremic</style></author><author><style face="normal" font="default" size="100%">Yulia B. Lazareva</style></author><author><style face="normal" font="default" size="100%">Alla M. Antsyshkina</style></author><author><style face="normal" font="default" size="100%">Tatiana V. Prostodusheva</style></author><author><style face="normal" font="default" size="100%">Roman M. Kuznetsov</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Research on External Signs and Chemical Composition of Medicinal Plant Raw Material -Leaves of Ficus Elastica</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chromato-mass spectrometry</style></keyword><keyword><style  face="normal" font="default" size="100%">Ficus elastic</style></keyword><keyword><style  face="normal" font="default" size="100%">Methyl</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytol</style></keyword><keyword><style  face="normal" font="default" size="100%">Vitamin E.</style></keyword><keyword><style  face="normal" font="default" size="100%">б-D-Glucopyranoside</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">958-972</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;em&gt;Ficus elastica &lt;/em&gt;is a species of the plant in the genus Ficus, from the family Moraceae. &lt;em&gt;Ficus elastica,&lt;/em&gt; which is the object of our study, has been used for many years in phytodesign, however in terms of medicine, it remains a poorly studied plant. While studying the external signs and chemical composition of medicinal plant raw materials of leaves&lt;em&gt; Fícus elastica&lt;/em&gt;, chromato-mass spectrometry was used. During the process of studying, some diagnostic signs of&lt;em&gt; Ficus elastica&lt;/em&gt; were identified. Chromato-mass spectrometry was used to identify 68 compounds. The maximum amount was accounted for &lt;em&gt;б-D-Glucopyranoside&lt;/em&gt;, methyl (28,99%), Phytol (9,90%), 2-Hydroxy-3-methylsuccinic acid (6,93%), Lanosterol (6,13%), Hydroquinone (5,55%), 9,12,15-Octadecatrienoic acid, ethyl ester, (Z,Z,Z)- (4,86%), Lup-20(29)-en-3- one (4,17%), 1,2-Benzenediol (3,33%), Lupeol (2,95%), 16-Allopregnene-3б,9а-diol-20-one 3-O-acetate (2,77%), 9-Octadecenamide, (Z)- (2,67%), 9,12,15-Octadecatrienoic acid, (Z,Z,Z)- (2,05%), з-Sitosterol (1,84%), а-d-Lyxofuranoside, methyl (1,57%), Dasycarpidan-1-methanol, acetate (ester) (1,52%), n-Hexadecanoic acid (1,45%), Hexadecanoic acid, ethyl ester (1,33%), 1,8-Dioxacyclohexadecane-2,10- dione, 5,6:12,13-diepoxy-8,16-dimethyl- (1,15%), &lt;em&gt;Vitamin E&lt;/em&gt; (0,64%). Identified morphological features of the leaves of &lt;em&gt;Ficus elastica &lt;/em&gt;can be used in diagnosis of this species and may help to develop indicators of authenticity for promising medicinal leaves. As mentioned earlier, by means of chromato-mass spectrometry were identified 68 compounds, and the relative percentage of identified compounds was determined using a simple normalization method.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><section><style face="normal" font="default" size="100%">958</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Angelina V. Strelyaeva&lt;sup&gt;1&lt;/sup&gt;, Anna G. Kharitonova&lt;sup&gt;1,*&lt;/sup&gt;, Larisa B. Vaskova&lt;sup&gt;1&lt;/sup&gt;, Alexander N. Luferov&lt;sup&gt;1&lt;/sup&gt;, Dmitry O. Bokov&lt;sup&gt;1&lt;/sup&gt;, Alina A. Bondar&lt;sup&gt;1&lt;/sup&gt;, Natalia V. Bobkova&lt;sup&gt;1&lt;/sup&gt;, Nevena Jeremic&lt;sup&gt;1,2&lt;/sup&gt;, Yulia B. Lazareva&lt;sup&gt;1&lt;/sup&gt;, Alla M. Antsyshkina&lt;sup&gt;1&lt;/sup&gt;, Tatiana V. Prostodusheva&lt;sup&gt;1&lt;/sup&gt;, Roman M. Kuznetsov&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Sechenov First Moscow State Medical University, 8, Trubetskaya St., bldg. 2, 119991, Russian Federation, RUSSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, SERBIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Swathi Priya K</style></author><author><style face="normal" font="default" size="100%">Rajasekaran S</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">RETRACTED: Phytochemical Screening, Gc-Ms Analysis and Antioxidant Activity of Marine Algae Obtained from Coastal Andhra Pradesh, India</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">GCMS analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Physicochemical.</style></keyword><keyword><style  face="normal" font="default" size="100%">Spongomorpha indica</style></keyword><keyword><style  face="normal" font="default" size="100%">Superoxide</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">641-649</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The Article has been Retracted based on the Authors' Request.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><accession-num><style face="normal" font="default" size="100%">23</style></accession-num><section><style face="normal" font="default" size="100%">641</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Swathi Priya K&lt;sup&gt;1,*&lt;/sup&gt;, Rajasekaran S&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Research Scholar, Department of Pharmacy, Bhagwant University, Sikar Rd, Ajmer, Rajasthan, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of pharmacology, Bhagwant University, Sikar Rd, Ajmer, Rajasthan, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arifia Safira</style></author><author><style face="normal" font="default" size="100%">Prasita Widayani</style></author><author><style face="normal" font="default" size="100%">Dhiya An-Najaaty</style></author><author><style face="normal" font="default" size="100%">Cinta Atsa Mahesa Rani</style></author><author><style face="normal" font="default" size="100%">Mela Septiani</style></author><author><style face="normal" font="default" size="100%">Yan Arengga Syah Putra</style></author><author><style face="normal" font="default" size="100%">Tridiganita Intan Solikhah</style></author><author><style face="normal" font="default" size="100%">Aswin Rafif Khairullah</style></author><author><style face="normal" font="default" size="100%">Hartanto Mulyo Raharjo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Review of an Important Plants: Annona squamosa Leaf</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Annona squamosa</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacology</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">Traditional medicinal plant</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">456-463</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Plants have been utilized extensively in traditional medicine by a range of nations since ancient times, and more research into their safety, efficacy, and quality value is needed. One of the plants that have been widely used by society in traditional medicine is Annona squamosa L. &lt;em&gt;A. squamosa &lt;/em&gt;is commonly cultivated in tropical and subtropical regions. Based on previous research, all parts of&lt;em&gt; A. squamosa&lt;/em&gt; including bark, leaf, and roots have proven biological activities such as antioxidant, antifungal, and anticancer, especially on the leaves. Indian people have long history used young leaves of &lt;em&gt;A. squamosa &lt;/em&gt;for antidiabetic, besides in South China, they use seeds to decrease the cancer effect in the human body. The pharmacological activities of &lt;em&gt;A. squamosa&lt;/em&gt; leaves are antimicrobial, antifungal, anti-inflammatory, anticancer, antiulcer, antidiabetic, antidiarrheals, antiplatelet, antioxidant, and hepatoprotective, neuroprotective, and cytoprotective. Phytochemicals in &lt;em&gt;A. squamosa&lt;/em&gt; leaves include coumarins, tannins, cardiac glycosides, flavonoids, carbohydrates, and saponins. Meanwhile based on nutritional analysis shows that the &lt;em&gt;A. squamosa &lt;/em&gt;leaves are water, protein, lipids, Fiber Ash and Calcium.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">456</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Arifia Safira&lt;sup&gt;1&lt;/sup&gt;, Prasita Widayani&lt;sup&gt;1&lt;/sup&gt;, Dhiya An-Najaaty&lt;sup&gt;1&lt;/sup&gt;, Cinta Atsa Mahesa Rani&lt;sup&gt;1&lt;/sup&gt;, Mela Septiani&lt;sup&gt;1&lt;/sup&gt;, Yan Arengga Syah Putra&lt;sup&gt;1&lt;/sup&gt;, Tridiganita Intan Solikhah&lt;sup&gt;1,*&lt;/sup&gt;, Aswin Rafif Khairullah&lt;sup&gt;2&lt;/sup&gt;, Hartanto Mulyo Raharjo&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Veterinary Clinic, Faculty of Veterinary Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Doctoral Program in Veterinary Science, Faculty of Veterinary Medicine, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Center of Excellence Fish Infectious Disease, Department of Veterinary Microbiology, Faculty of Veterinary Science, Chulalongkorn University, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ditya Indrawati</style></author><author><style face="normal" font="default" size="100%">Linda Astari</style></author><author><style face="normal" font="default" size="100%">Afif Nurul Hidayati</style></author><author><style face="normal" font="default" size="100%">Sawitri, Damayanti</style></author><author><style face="normal" font="default" size="100%">Budi Utomo</style></author><author><style face="normal" font="default" size="100%">Bagus Haryo Kusumaputra</style></author><author><style face="normal" font="default" size="100%">Medhi Denisa Alinda</style></author><author><style face="normal" font="default" size="100%">Cita Rosita Sigit Prakoeswa</style></author><author><style face="normal" font="default" size="100%">M. Yulianto Listiawan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Risk Factors of Acute and Chronic Erythema Nodosum Leprosum in Dr. Soetomo General Academic Hospital Surabaya</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acute ENL</style></keyword><keyword><style  face="normal" font="default" size="100%">Chronic ENL</style></keyword><keyword><style  face="normal" font="default" size="100%">ENL</style></keyword><keyword><style  face="normal" font="default" size="100%">Leprosy</style></keyword><keyword><style  face="normal" font="default" size="100%">Neglected disease.</style></keyword><keyword><style  face="normal" font="default" size="100%">Risk factors</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">766-770</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Leprosy is a chronic granulomatous infection and is one of the neglected diseases caused by &lt;em&gt;Mycobacterium leprae.&lt;/em&gt; ENL is a complex syndrome, that caused inflammation of the skin, nerves, and other organs due to an inflammatory immune response to &lt;em&gt;Mycobacterium leprae &lt;/em&gt;antigens. Acute ENL was defined as the first episode of ENL with a duration of less than 24 weeks. Chronic ENL was defined as ENL that persisted for more than 24 weeks. These types of ENL can have different risk factors and require different therapeutic interventions. Purpose: The onset of ENL is acute, but may progress to a chronic or recurrent phase and require long-term therapy. Early detection of leprosy is very important, because the infection is curable and prompt treatment can reduce nerve damage and associated stigma. Chronic ENL patients require prolonged high doses of corticosteroids to control inflammation in ENL and cause severe complications and side effects associated with morbidity and mortality.&lt;strong&gt; Methods: &lt;/strong&gt;This retrospective study was conducted using a non-probability sampling technique consecutively using a casecontrol formula in leprosy patients with ENL in the Leprosy Division of the Outpatient Dermatology and Venereology Unit RSUD Dr. Soetomo Surabaya for the period 2015 – 2020, using secondary data in the form of medical record data.&lt;strong&gt; Result: &lt;/strong&gt;The results of this study obtained leprosy patients with ENL as many as 234 patients, 56 patients with acute ENL and 89 patients with chronic ENL. 45 patients with acute ENL and 45 patients with chronic ENL were obtained from the case-control minimal sample size formula. &lt;strong&gt;Conclusion:&lt;/strong&gt; The results of the bivariate analysis test showed that there was a relationship between risk factors for coinfection and steroid therapy with the type of ENL. The presence of coinfection and steroid therapy showed that patients tend to be chronic ENL, conversely, in the absence of coinfection and without steroid therapy, patients tend to be acute ENL. The multivariate logistic regression analysis test showed a significant association between risk factors for ENL onset before MDT and the presence of coinfection with chronic ENL, whereas ENL onset after MDT and absence of coinfection were associated with acute ENL.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">766</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ditya Indrawati, Linda Astari, Afif Nurul Hidayati, Sawitri, Damayanti, Budi Utomo, Bagus Haryo Kusumaputra, Medhi Denisa Alinda, Cita Rosita Sigit Prakoeswa, M. Yulianto Listiawan*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Resident of Dermatology and Venereology, Faculty of Medicine, Universitas Airlangga/ Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Diny Kamilah</style></author><author><style face="normal" font="default" size="100%">Berna Elya</style></author><author><style face="normal" font="default" size="100%">Robiatul Adawiyah</style></author><author><style face="normal" font="default" size="100%">Annysa Ellycornia Silvyana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Senna Siamea Hexane Extract: Potent Antifungal Activity Against Candida albicans, Candida Krusei and Identification of Its Chemicals Content</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antifungal</style></keyword><keyword><style  face="normal" font="default" size="100%">Chemical content.</style></keyword><keyword><style  face="normal" font="default" size="100%">Hexane extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Senna siamea</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2023</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">999-1004</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt;&lt;em&gt; Senna siamea&lt;/em&gt; contains several chemical: flavonoid, steroids, terpenoids, alkaloid, and tanin which is as an antifungal againts of Candida sp because interfere function of the fungal cell membrane and inhibit syntesis of chitin. Candida albicans and Candida krusei could causing oral candidiasis, vulvovaginal infections, life threatening candidiasis, such as candidemia and internal organ infections&lt;em&gt;. S. siamea&lt;/em&gt; is a medicinal plant which empirically used as antifungal. &lt;em&gt;S. siamea &lt;/em&gt;leaves has been reported to exhibit activity against Candida sp but limited to ethanol extract. Thus, the evaluation of other extract- and identification of active compound(s) against&lt;em&gt; C. albicans&lt;/em&gt; and&lt;em&gt; C. krusei &lt;/em&gt;is needed to be explore. &lt;strong&gt;Methods:&lt;/strong&gt; First, the microscopic morphology of&lt;em&gt; S. siamea &lt;/em&gt;leaves were observed using Scanning Electron Microscope. The leaves were then extracted sequentially by hexane, ethyl acetate, and methanol solvent using the ultrasonic assisted extraction method, followed by its&lt;em&gt; in vitro &lt;/em&gt;antifungal activity evaluation. The most active extract was further evaluated for its chemical(s) content by LC MS. &lt;strong&gt;Results:&lt;/strong&gt; Scanning Electron Microscope identified the presence of oxalate in the leaves of&lt;u&gt; S. siamea&lt;/u&gt;. Evaluation of the antifungal activity showed that the hexane extract had highest antifungal compared to others.&lt;strong&gt; Conclusions:&lt;/strong&gt; &lt;em&gt;S. siamea &lt;/em&gt;hexane extract leaf is prospective to be developed as an antifungal. Further in vivo research are needed.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Research Article </style></work-type><section><style face="normal" font="default" size="100%">999</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Diny Kamilah&lt;sup&gt;1&lt;/sup&gt;, Berna Elya1, Robiatul Adawiyah&lt;sup&gt;2,*&lt;/sup&gt;, Annysa Ellycornia Silvyana&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Pharmacy, Universitas Indonesia, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Parasitology Department , Faculty of Medicine, Universitas Indonesia, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Study Program of Pharmacy, Sekolah Tinggi Ilmu Kesehatan Medistra Indonesia&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kebede Feyisa</style></author><author><style face="normal" font="default" size="100%">Wondu Feyisa</style></author><author><style face="normal" font="default" size="100%">Ture Girma</style></author><author><style face="normal" font="default" size="100%">Teyiba Kemal</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Traditional Medicinal Plants Used for the Treatment of Urological and Urogenital Diseases in Ethiopia: A Review</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ethiopia.</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethnobotany</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal plants</style></keyword><keyword><style  face="normal" font="default" size="100%">Traditional medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Urological diseases</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">722-733</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Ethiopia is recognized as one of the richest biodiversity in Africa. The present review aimed to compile relevant information on medicinal plants traditionally used to manage urogenital diseases in Ethiopia. &lt;strong&gt;Methods:&lt;/strong&gt; Different literatures published specifically on ethnobotanical use of medicinal plants in scientific journals, books, theses and proceedings were reviewed. Data from literatures were analyzed using statistical package for social sciences (SPSS) Version 20 and an Excel spreadsheet and reported using descriptive statistics, frequency, and percentage. &lt;strong&gt;Results&lt;/strong&gt;: A total of 146 medicinal plants are reported in the reviewed literature. It was distributed in 127 genera and 64 families.&lt;em&gt; Cucurbitaceae&lt;/em&gt; (7.51%), Asteriaceae (7.51%), &lt;em&gt;Euphorbaceae&lt;/em&gt; (6.20%) and &lt;em&gt;Apiaceae &lt;/em&gt;(4.80%) were family’s accounts of high number of species. A higher diversity of medicinal plants was reported from Southern nations and nationalities (44.5%), Oromia (41.1%) and Amhara (27.4%) regional states. The most frequently reported growth form of medicinal plants indicated in the review was herbs (46.8%), followed by shrubs (32.6%). Root (36.2%) and leaves (35.3%) were the most used parts. Decoction (26.1%), concoction (16.5%) and pounding (11.9%) were the most frequently reported remedy preparation methods and were administered orally.&lt;strong&gt; Conclusion: &lt;/strong&gt;The present review indicated that urogenital diseases were managed with different medicinal plants throughout the regions of Ethiopian needed scientifically confirmed in order to produce safe and effective drugs from natural products.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><accession-num><style face="normal" font="default" size="100%">32</style></accession-num><section><style face="normal" font="default" size="100%">722</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kebede Feyisa&lt;sup&gt;1,*&lt;/sup&gt;, Wondu Feyisa&lt;sup&gt;2&lt;/sup&gt;, Ture Girma&lt;sup&gt;3&lt;/sup&gt;, Teyiba Kemal&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of pharmacy, College of Medicine and Health Sciences, Bahir Dar University, Bahir Dar, ETHIOPIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Midwifery, College of Medicine and Health Sciences, Bahir Dar University, Bahir Dar, ETHIOPIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biology, College of Natural and Computational Sciences, Dilla University, Dilla, ETHIOPIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacy, College of Health and Medical Science, Haramaya University, Harar, ETHIOPIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">AF Dibha</style></author><author><style face="normal" font="default" size="100%">S Wahyuningsih</style></author><author><style face="normal" font="default" size="100%">ANM Ansori</style></author><author><style face="normal" font="default" size="100%">VD Kharisma</style></author><author><style face="normal" font="default" size="100%">MH Widyananda</style></author><author><style face="normal" font="default" size="100%">AA Parikesit</style></author><author><style face="normal" font="default" size="100%">MT Sibero</style></author><author><style face="normal" font="default" size="100%">RT Probojati</style></author><author><style face="normal" font="default" size="100%">AAA Murtadlo</style></author><author><style face="normal" font="default" size="100%">JP Trinugroho</style></author><author><style face="normal" font="default" size="100%">TH Sucipto</style></author><author><style face="normal" font="default" size="100%">DDR Turista</style></author><author><style face="normal" font="default" size="100%">I Rosadi</style></author><author><style face="normal" font="default" size="100%">ME Ullah</style></author><author><style face="normal" font="default" size="100%">V Jakhmola</style></author><author><style face="normal" font="default" size="100%">R Zainul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Utilization of Secondary Metabolites in Algae Kappaphycus alvarezii as a Breast Cancer Drug with a Computational Method</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Breast cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">K. alvarezii</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular Docking.</style></keyword><keyword><style  face="normal" font="default" size="100%">NF kB protein kinase</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2022</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">14</style></volume><pages><style face="normal" font="default" size="100%">536-543</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Breast cancer is one of the worst diseases that affect female people. Long-term treatment with therapy or surgery has a detrimental impact on the patient. The algae &lt;em&gt;Kappaphycus alvarezii&lt;/em&gt; has gotten a lot of interest as a breast cancer medication because it contains chemicals that are expected to be anti-cancer. The objectives of this paper were to see how secondary metabolites in algae interact with the Nuclear Factor- kappaB protein kinase in breast cancer. The ligands and proteins were obtained from the PubChem and PDB websites, respectively. Swiss ADME was then used to assess the Pharmacokinetics and Drug likeness Properties. The last stage involved using molecular docking with PyRx and molecular dynamics to identify the interaction and visualization between the ligand and the target protein. The findings of the test revealed that the maraniol chemical had a superior binding capacity with NF kB protein kinase because it has a chromone group that controls transport efficiently in preventing breast cancer proliferation.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><accession-num><style face="normal" font="default" size="100%">08</style></accession-num><section><style face="normal" font="default" size="100%">536</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;AF Dibha&lt;sup&gt;1&lt;/sup&gt;, S Wahyuningsih&lt;sup&gt;2&lt;/sup&gt;, ANM Ansori&lt;sup&gt;3&lt;/sup&gt;, VD Kharisma&lt;sup&gt;4&lt;/sup&gt;, MH Widyananda&lt;sup&gt;4,5&lt;/sup&gt;, AA Parikesit&lt;sup&gt;6&lt;/sup&gt;, MT Sibero&lt;sup&gt;7&lt;/sup&gt;, RT Probojati&lt;sup&gt;4,8&lt;/sup&gt;, AAA Murtadlo&lt;sup&gt;4&lt;/sup&gt;, JP Trinugroho&lt;sup&gt;9&lt;/sup&gt;, TH Sucipto&lt;sup&gt;10&lt;/sup&gt;, DDR Turista&lt;sup&gt;11&lt;/sup&gt;, I Rosadi&lt;sup&gt;12&lt;/sup&gt;, ME Ullah&lt;sup&gt;13,&lt;/sup&gt; V Jakhmola&lt;sup&gt;14&lt;/sup&gt;, R Zainul&lt;sup&gt;15,16,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Brawijaya University, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Biology, Gadjah Mada University, Yogyakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Professor Nidom Foundation, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Division of Molecular Biology and Genetics, Generasi Biologi Indonesia Foundation, Gresik, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences, Brawijaya University, Malang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Bioinformatics, School of Life Sciences, Indonesia International Institute for Life Sciences, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Marine Science, Faculty of Fisheries and Marine Science, Universitas Diponegoro, Semarang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Faculty of Agriculture, Universitas Kadiri, Kediri, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;9&lt;/sup&gt;Department of Life Sciences, Imperial College London, South Kensington Campus, London, UNITED KINGDOM.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;10&lt;/sup&gt;Dengue Study Group, Institute of Tropical Disease, Universitas Airlangga, Surabaya, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;11&lt;/sup&gt;Biology Education Department, Faculty of Teacher Training and Education, Mulawarman University, Samarinda, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;12&lt;/sup&gt;Department of Biology, Faculty of Mathematics and Natural Sciences, Mulawarman University, Samarinda, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;13&lt;/sup&gt;Department of Chemistry, Mississippi State University, Mississippi State, UNITED STATES.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;14&lt;/sup&gt;Uttaranchal Institute of Pharmaceutical Sciences, Uttaranchal University, Dehradun, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;15&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;16&lt;/sup&gt;Center for Advanced Material Processing, Artificial Intelligence, and Biophysic Informatics (CAMPBIOTICS), Universitas Negeri Padang, Padang, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Liudmyla Zotsenko</style></author><author><style face="normal" font="default" size="100%">Nataliia Nuzhyna</style></author><author><style face="normal" font="default" size="100%">Viktoria Kyslychenko</style></author><author><style face="normal" font="default" size="100%">Oksana Futorna</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anatomical and Ultrastructure Differences Between Some Species of the Genus Elsholtzia Willd. of Flora of Ukraine</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Elsholtzia ciliate</style></keyword><keyword><style  face="normal" font="default" size="100%">Elsholtzia stauntonii</style></keyword><keyword><style  face="normal" font="default" size="100%">Leaf anatomy</style></keyword><keyword><style  face="normal" font="default" size="100%">Petal</style></keyword><keyword><style  face="normal" font="default" size="100%">Petiole</style></keyword><keyword><style  face="normal" font="default" size="100%">Stem</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">977-987</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Elsholtzia&lt;/em&gt; species are very popular in Chinese, Tibetan and Vietnamese folk medicine to treat several diseases. Despite the wide range of biological activity and the study of the chemical composition of individual species, the microscopic characteristics of plants of this genus are insufficiently studied. In the article the anatomical structure of two species &lt;em&gt;Elsholtzia &lt;/em&gt;Willd. of flora of Ukraine is represented. The sources of literature provide only a morphological description of &lt;em&gt;Elsholtzia&lt;/em&gt; &lt;em&gt;stauntonii&lt;/em&gt; and &lt;em&gt;Elsholtzia ciliate.&lt;/em&gt; We analyzed crosssections and ultrastructure of leaf blade, petiole, petal and stem, determined their anatomical features, and investigated the ultrastructure of seeds. We have compared the obtained data between this two species of this genus that grow on the territory of Ukraine under similar conditions. &lt;strong&gt;Methods:&lt;/strong&gt; Microscopic analysis was carried out by the well-known methods using the microscope XSP-146TR and ImageJ program. Anatomical structure of &lt;em&gt;Elsholtzia stauntonii&lt;/em&gt; Benth. and&lt;em&gt; Elsholtzia&lt;/em&gt; ciliate Thun. are studied and main diagnostic features are highlighted. The ultrastructure of the surface of the epidermal tissue of leaves, stems and seeds were studied additionally, using scanning microscopy methods. &lt;strong&gt;Results: &lt;/strong&gt;The diagnostic microscopic distinguishing features of &lt;em&gt;E. ciliate &lt;/em&gt;raw material from &lt;em&gt;E. stauntonii &lt;/em&gt;are: the presence of small glandular triсhomes, singly placed on the veins and the presence of long non glandular triсhomes on the central vein of abaxial side. Non glandular triсhomes of &lt;em&gt;E. ciliate &lt;/em&gt;are three times longer compared to another investigated species. The presence of numerous triсhomes and massive clusters of stem sclerenchyma &lt;em&gt;E. stauntonii &lt;/em&gt;can be considered additional taxonomic criteria for comparing the studied species.&lt;strong&gt; Conclusion:&lt;/strong&gt; The practical significance of our research will use to develop of quality control methods for medicinal herbal raw material – «Herba &lt;em&gt;Elsholtziae&lt;/em&gt; Stauntonii», «Herba &lt;em&gt;Elsholtziae &lt;/em&gt;ciliate».&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">977</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Liudmyla Zotsenko&lt;sup&gt;1,&lt;/sup&gt;*, Nataliia Nuzhyna&lt;sup&gt;2&lt;/sup&gt;, Viktoria Kyslychenko&lt;sup&gt;3&lt;/sup&gt;, Oksana Futorna&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;State Laboratory of Quality Control of Medicines, State Institution, Institute of Pharmacology and Toxicology National Academy of Medical Sciences of Ukraine, Kyiv, UKRAINE.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;NSC &quot;Institute of Biology and Medicine&quot; Taras Shevchenko National University of Kyiv, Kyiv, UKRAINE.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;National University of Pharmacy, Department of Chemistry of Natural Compounds, Kharkiv, UKRAINE.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sisilia Teresia Rosmala Dewi</style></author><author><style face="normal" font="default" size="100%">M Sabir</style></author><author><style face="normal" font="default" size="100%">Sesilia Rante Pakadang</style></author><author><style face="normal" font="default" size="100%">Sainal Edi Kamal</style></author><author><style face="normal" font="default" size="100%">Santi Sinala</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anti-Cancer Potential of Nggorang Leaves Extract (Salvia Occidentalis SW.) as a Protein P53 Supressor in T47D Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anticancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Nggorang Leaves Extract (Salvia occidentalis Sw)</style></keyword><keyword><style  face="normal" font="default" size="100%">Protein P53</style></keyword><keyword><style  face="normal" font="default" size="100%">T47D</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1036-1045</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Breast cancer is one of the most common types of cancer in women. The high incidence of breast cancer has led to the development of anticancer drugs that are more selective against cancer cells without damaging normal tissues. One of the alternatives in cancer treatment by looking for natural sources that can be developed, Nggorang leaves (&lt;em&gt;Salvia occidentalis &lt;/em&gt;Sw.). This plant is found in Tenda Village, Langke Rembong District, Manggarai Regency, NTT Province, when the leaves are harvested for one year and are used as medicine. As a preventive, this leaf has been used for generations as an anticancer (7 leaves boiled with 200 ml of water to 100 ml and then drunk), for wounded breast cancer (crushed leaves and attached to the wound); stamina enhancer, cough, influenza, hemorrhoids, diarrhea, nosebleeds (Primary data, 2014). This study aims to prove the potential of EDG (Nggorang Leaves Extract) as an antiproliferative against Hela cancer cells and protein P53 suppressor. The method used is the Quasy experiment, because this study uses laboratory tests in sample testing. The results of the cytotoxic test of Nggorang Leaves Extract have the potential to be anti-proliferative against cancer cells T47D IC50 at 201 ppm and Nggorang Leaves Extract (EDG) has the potential to increase p53 gene suppression in T47D cancer cells by 94.13% at a concentration of 50 ppm.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1036</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sisilia Teresia Rosmala Dewi&lt;sup&gt;1&lt;/sup&gt;, M. Sabir&lt;sup&gt;2&lt;/sup&gt;, Sesilia Rante Pakadang&lt;sup&gt;1&lt;/sup&gt;, Sainal Edi Kamal&lt;sup&gt;3&lt;/sup&gt;, Santi Sinala&lt;sup&gt;1,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Health Polytechnic of the Makassar Ministry of Health, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Medicine University of Tadulako Palu, INDONESIA. 3Polytechnic Sandi Karsa Makassar, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Maulana Yusuf Alkandahri</style></author><author><style face="normal" font="default" size="100%">Dani Sujana</style></author><author><style face="normal" font="default" size="100%">Dadang Muhammad Hasyim</style></author><author><style face="normal" font="default" size="100%">Mareetha Zahra Shafirany</style></author><author><style face="normal" font="default" size="100%">Lela Sulastri</style></author><author><style face="normal" font="default" size="100%">Maya Arfania</style></author><author><style face="normal" font="default" size="100%">Dedy Frianto</style></author><author><style face="normal" font="default" size="100%">Farhamzah</style></author><author><style face="normal" font="default" size="100%">Anggun Hari Kusumawati</style></author><author><style face="normal" font="default" size="100%">Nia Yuniarsih</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antidiabetic Activity of Extract and Fractions of Castanopsis costata Leaves on Alloxan-induced Diabetic Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antidiabetic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Castanopsis costata</style></keyword><keyword><style  face="normal" font="default" size="100%">Diabetes mellitus</style></keyword><keyword><style  face="normal" font="default" size="100%">North Sumatra.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1589-1593</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;In North Sumatra, Castanopsis costata is commonly used by traditional practitioners for the treatment of diabetes mellitus, however, no studies have been carried out to substantiate this practice. Therefore, this study aims to evaluate the anti-diabetic activity of extract and fractions of C. costata leaves in mice with alloxan-induced diabetes. &lt;strong&gt;Methods:&lt;/strong&gt; Swiss albino mice with alloxan-induced diabetes, were acquired and subjected to the experimental evaluations. Subsequently, the fasting blood glucose levels of the diabetic mice groups treated with glibenclamid, extract and fractions, as well as the untreated group, were evaluated after two weeks of therapy. &lt;strong&gt;Results: &lt;/strong&gt;Based on the results, the ethanolic extract of C. costata considerably reduced the mice’s blood glucose levels in a dose-dependent manner, at dosages of 25, 50, 100, and 200 mg/kgBW (% DBGL: 21.10%, 46.36%, 58.94%, and 60.93%, respectively). In addition, the water fraction of C. costata leaves produced a greater reduction in blood glucose levels (% DBGL: 78.93%), compared to the ethyl acetate and n-hexane fractions (% DBGL: 67.06% and 58.83%), respectively. Meanwhile, treatment with the antidiabetic drug, glibenclamide (5 mg/kgBW) produced a 50.75% reduction in blood glucose levels. &lt;strong&gt;Conclusion: &lt;/strong&gt;Based on the findings, the extract and fractions of C. costata leaves were concluded to exhibit significant anti-diabetic activity. This supported the claim that traditional practitioners in North Sumatra use the plant extract for diabetes treatment.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1589</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Maulana Yusuf Alkandahri&lt;sup&gt;1&lt;/sup&gt;,&lt;sup&gt;*&lt;/sup&gt;, Dani Sujana&lt;sup&gt;2&lt;/sup&gt;, Dadang Muhammad Hasyim&lt;sup&gt;2&lt;/sup&gt;, Mareetha Zahra Shafirany&lt;sup&gt;3&lt;/sup&gt;, Lela Sulastri&lt;sup&gt;4&lt;/sup&gt;, Maya Arfania&lt;sup&gt;1&lt;/sup&gt;, Dedy Frianto&lt;sup&gt;1&lt;/sup&gt;, Farhamzah&lt;sup&gt;1&lt;/sup&gt;, Anggun Hari Kusumawati&lt;sup&gt;1&lt;/sup&gt;, Nia Yuniarsih&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Pharmacy, Buana Perjuangan Karawang University, Karawang, West Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Diploma Program of Pharmacy, Karsa Husada Garut College of Health Sciences, Garut, West Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmaceutical Biology, School of Pharmacy Muhammadiyah Cirebon, Cirebon, West Java, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmaceutics and Pharmaceutical Technology, School of Pharmacy Muhammadiyah Cirebon, Cirebon, West Java, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aseel Aljaghwani</style></author><author><style face="normal" font="default" size="100%">Khaled S Allemailem</style></author><author><style face="normal" font="default" size="100%">Lujain F Aljaghwani</style></author><author><style face="normal" font="default" size="100%">Faris Alrumaihi</style></author><author><style face="normal" font="default" size="100%">Rejo Jacob Joseph</style></author><author><style face="normal" font="default" size="100%">Amjad Ali Khan</style></author><author><style face="normal" font="default" size="100%">Mohammad aljaghwani</style></author><author><style face="normal" font="default" size="100%">Arshad H Rahmani</style></author><author><style face="normal" font="default" size="100%">Ahmad Almatroudi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antimicrobial Effect of Different Types of Honey on Selected ATCC Bacterial Strains</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Enterococcus faecalis</style></keyword><keyword><style  face="normal" font="default" size="100%">Staphylococcus aureus</style></keyword><keyword><style  face="normal" font="default" size="100%">Talha honey</style></keyword><keyword><style  face="normal" font="default" size="100%">Zahoor honey and Manuka honey</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">217-225</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Honey is a complex sweet highly viscous liquid and is composed of various ingredients such as sugar, proteins, minerals, and polyphenolic compounds. Honey is used in traditional medicine systems for centuries because of its ability to inhibit the pathogenesis of various diseases through modulating various biological activities. In this study, antimicrobial potential of different types of honey was tested against selected pathogenic bacterial strains through agar well diffusion method. Four types of honey were used in the present investigation, and the potential antimicrobial activities of these varieties were further compared with that of antibiotics commonly used against targeted microbial strains. Among all of the four tested honey, three types were classified as blossom honey, being Talha (&lt;em&gt;Acacia &lt;/em&gt;sp) honey (TH), Zahoor (mixed flower) honey (ZH), and Manuka (&lt;em&gt;Leptospermum &lt;/em&gt;based honey) honey (MH). Both gram positive and gram negative bacterial species were used for this investigation. The pathogenic gram-positive bacterial strains included&lt;em&gt;Escherichia coli&lt;/em&gt; ATCC 29213, Enterococcus faecalis ATCC 29212 and methicillin-resistant Staphylococcus (MRSA) ATCC 43300. Three gram negative bacteria like &lt;em&gt;Escherichia coli&lt;/em&gt; ATCC 25922,&lt;em&gt; Klebsiella pneumonia&lt;/em&gt; ATCC 700603 and &lt;em&gt;Pseudomonas aeruginosa&lt;/em&gt; ATCC 27853 were also used to confirm the antimicrobial activities. As reflected from our study, we found that three varieties of honey including TH, ZH, and MH (with different UMF +20, +16, +5) displayed a broad spectrum antibacterial activity against all tested microbial strains. However, all strains showed a high frequency of resistance to BF honey. Gram-positive (G+) bacteria were found to be more sensitive to all tested honey types except (BF) as indicated by significantly higher zone of inhibition (ZOI) values than those of gram-negative (G-) bacteria. As a conclusion, this study suggests that antimicrobial potential of honey types might be helpful in order to treat the pathogenic microorganisms threatening the public health and changing antibiotics into last-resort drugs.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">217</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Aseel Aljaghwani&lt;sup&gt;1&lt;/sup&gt;, Khaled S Allemailem&lt;sup&gt;1&lt;/sup&gt;, Lujain F. Aljaghwani&lt;sup&gt;2&lt;/sup&gt;, Faris Alrumaihi&lt;sup&gt;1&lt;/sup&gt;, Rejo Jacob Joseph&lt;sup&gt;3&lt;/sup&gt;, Amjad Ali Khan&lt;sup&gt;3&lt;/sup&gt;, Mohammad aljaghwani&lt;sup&gt;4&lt;/sup&gt;, Arshad H. Rahmani&lt;sup&gt;1&lt;/sup&gt;, Ahmad Almatroudi&lt;sup&gt;1,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, SAUDI ARABIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Obstetrics and Gynecology, Maternity and Children Hospital, Buraydah, SAUDI ARABIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Basic Health Sciences, College of Applied Medical Sciences, Qassim University, Buraydah, SAUDI ARABIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Cardiovascular and Catheter Laboratory, Prince Sultan Center for Cardiac Medicine and Surgery, Buraydah, SAUDI ARABIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Joseph M Kathare</style></author><author><style face="normal" font="default" size="100%">James M Mbaria</style></author><author><style face="normal" font="default" size="100%">Joseph M Nguta</style></author><author><style face="normal" font="default" size="100%">Gervason A Moriasi</style></author><author><style face="normal" font="default" size="100%">Alfred O Mainga</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antimicrobial Efficacy, Cytotoxicity, Acute Oral Toxicity, and Phytochemical Investigation of the Aqueous and Methanolic Stem Bark Extracts of Bridellia micrantha (Hochst.) Baill</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Brine shrimp lethality Assay</style></keyword><keyword><style  face="normal" font="default" size="100%">Median lethal concentration (LC50)</style></keyword><keyword><style  face="normal" font="default" size="100%">median lethal dose (LD50)</style></keyword><keyword><style  face="normal" font="default" size="100%">Minimum inhibitory concentration</style></keyword><keyword><style  face="normal" font="default" size="100%">Zone of Inhibition</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1248-1256</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Microbial infections cause high morbidity and mortality in humans globally. Antimicrobial resistance, emergence of new strains, high costs of antibiotics, inaccessibility-especially in remote areas, and adverse effects, impede successful eradications of pathogens, hence the need for novel strategies. &lt;em&gt;Bridellia micrantha&lt;/em&gt; is used in traditional medicine to treat microbial infections; however, it has not been empirically validated.&lt;strong&gt; Methods:&lt;/strong&gt; Antimicrobial activity of the aqueous and methanolic stem bark extracts of &lt;em&gt;Bridellia micrantha&lt;/em&gt; was investigated using the disk diffusion and broth microdilution techniques, described by the Clinical Laboratory Standards Institute (CLSI) guidelines. The brine shrimp lethality assay technique was used to investigate the cytotoxic effects of the studied plant extracts in exposed nauplii. Acute oral toxicity effects of the studied plant extracts in Winstar rats were investigated following the up-and-down procedure described by the Organisation for Economic Development and Co-operation (OECD). Qualitative phytochemical screening was performed following standard procedures. &lt;strong&gt;Results: &lt;/strong&gt;The aqueous and methanolic extract of B. micrantha indicated varied antimicrobial activities against &lt;em&gt;E. coli, S. typhimurium, S. aureus,&lt;/em&gt; and &lt;em&gt;C. albicans,&lt;/em&gt; with inhibition zones ranging from 6.00mm to 19.00mm. Furthermore, the studied plant extracts exhibited low MIC values (≤100 μg/ml) on selected microbes. Since the MIC values were much lower than 1000μg/ml (the cutoff for antimicrobial efficacy appraisal), it is anticipated that, the studied plant extracts can be strong antibiotics. The aqueous and methanolic stem bark extracts of &lt;em&gt;B. micrantha&lt;/em&gt; were cytotoxic to brine shrimp nauplii, with LC50 values of 486.67±3.15 μg/ml and 458.33±2.87 μg/ml, respectively; however, these extracts did not elicit any observable signs of toxicity in rat models. Pharmacologically active phytochemicals, including flavonoids, alkaloids, saponins, tannins, phenols, and anthraquinones were detected in the two studied extracts.&lt;strong&gt; Conclusions:&lt;/strong&gt; The aqueous and methanolic stem bark extracts of &lt;em&gt;B. micrantha&lt;/em&gt; have appreciable antimicrobial activity against &lt;em&gt;E. coli, S. typhimurium, S. aureus&lt;/em&gt; and &lt;em&gt;C. albicans&lt;/em&gt;. Besides, the studied plant extracts are cytotoxic to brine shrimp nauplii; but they do not cause acute oral toxicity effects in rat models. Additionally, the studied plant extracts contain bioactive phytochemicals, with antimicrobial activity.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1248</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Joseph M. Kathare&lt;sup&gt;1,&lt;/sup&gt;*, James M. Mbaria&lt;sup&gt;1&lt;/sup&gt;, Joseph M. Nguta&lt;sup&gt;1&lt;/sup&gt;, Gervason A. Moriasi&lt;sup&gt;2&lt;/sup&gt;, Alfred O. Mainga&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Public Health, Pharmacology, and Toxicology, College of Veterinary and Agricultural Sciences, University of Nairobi, P.O. Box 29053- 00625, Nairobi, KENYA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medical Biochemistry, School of Medicine, College of Health Sciences, Mount Kenya University, P.O. 342-01000, Thika, KENYA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Iman A. A. Kassem</style></author><author><style face="normal" font="default" size="100%">Sally A. El Awdan</style></author><author><style face="normal" font="default" size="100%">Dalia O. Saleh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Characterization of Flavonoids and Saponins from Gleditsia triacanthos by LC-ESI/MS/MS Analysis: Pharmacological Assessment of the Anti-hyperglycemic and Anti-ulcerogenic Activities of G. triacanthos methanolic Fruit Extract and its n-Butanol Fraction</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-diabetic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Gleditsia triacanthos</style></keyword><keyword><style  face="normal" font="default" size="100%">Hypoglycemic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Ulceroprotective effect</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">631-639</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;&lt;em&gt;Gleditsia triacanthos&lt;/em&gt; is known to possess various pharmacological activities. &lt;strong&gt;Objective: &lt;/strong&gt;The composition of n-butanol fraction of &lt;em&gt;Gleditsia triacanthos &lt;/em&gt;methanolic seedless fruit extract was identified from the LC-ESI/MS/MS spectra. Total methanolic extract of the seedless &lt;em&gt;G. triacanthos&lt;/em&gt; fruits (MEGT) and its n-butanol fraction (BFGT) at three dose levels 70, 140 and 280 mg/kg were studied for their anti-diabetic and anti-ulcerogenic effects. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The anti-diabetics properties of MEGT and BFGT were orally assessed in streptozotocin (STZ; 55 mg/kg; i.p.)-induced hyperglycemic rats. Their anti-ulcerogenic activities were also evaluated in ethanol-induced peptic ulcer in rats.&lt;strong&gt; Results:&lt;/strong&gt; Two phenolic acids, five flavonoids as well as four saponins were identified from BFGT. Both MEGT and BFGT showed high potential in decreasing the elevated serum glucose, total triglycerides and total cholesterol levels in rats, dose dependently, comparable with the anti-diabetic reference drug; gliclazide (Glz; 10 mg/kg; p.o.). They also showed an elevation insulin and α-amylase serum levels. On the other hand, MEGT and BFGT showed significant ulceroprotective activities through decreasing both number and severity of ethanol-induced gastric lesions in rats, dose dependently, comparable with the anti-ulcer reference drug; ranitidine (20 mg/kg; p.o.) with MEGT at 280 mg/kg showing highest activity. &lt;strong&gt;Conclusion:&lt;/strong&gt; From all the previous results, it can be concluded that the observed pharmacological properties are attributed to the augmented activities of the saponin and flavonoidal content of G. triacanthos fruits.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">631</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Iman A. A. Kassem&lt;sup&gt;1&lt;/sup&gt;, Sally A. El Awdan&lt;sup&gt;2&lt;/sup&gt;, Dalia O. Saleh&lt;sup&gt;2,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Chemistry of Natural Compounds Department, National Research Centre, Dokki, Cairo 12622, EGYPT.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacology Department, National Research Centre, Dokki, Cairo 12622, EGYPT.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rima Farah AOUAD</style></author><author><style face="normal" font="default" size="100%">Mokhtaria Yasmina BOUFADI</style></author><author><style face="normal" font="default" size="100%">Djallal Eddine Houari ADLI</style></author><author><style face="normal" font="default" size="100%">Faiza MOULAI-HACENE</style></author><author><style face="normal" font="default" size="100%">Khaled KAHLOULA</style></author><author><style face="normal" font="default" size="100%">Miloud SLIMANI</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chemical Composition and Protective Effect of Rosmarinus officinalis on Alcohol-Induced Serum Hepatic Changes and Liver Injury in Male Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ethylism</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC/UV</style></keyword><keyword><style  face="normal" font="default" size="100%">Liver stress oxidatives</style></keyword><keyword><style  face="normal" font="default" size="100%">Rosmarinus officinalis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1205-1215</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Is a pleasant-smelling perennial shrub that grows in many parts of the world, &lt;em&gt;Rosmarinus officinalis &lt;/em&gt;a well known valuable herbal medicine which is widely used in pharmaceuticals and traditional medicine as a digestive, tonic, astringent, diuretic, diaphoretic and useful for urinary ailments. &lt;strong&gt;Objective: &lt;/strong&gt;The objective of this study has, on the one hand, focused on the changes in hepatotoxicity induced by the chronic administration of ethyl alcohol according to a biochemical and histological experimental approach and, on the other hand, on the chemical composition which was determined. As well as, the hepato-protective effect of the ethanolic extract of &lt;em&gt;Rosmarinus officinalis &lt;/em&gt;(EER), whether to restore or not the harmful alterations due to ethylism was evaluated. &lt;strong&gt;Method: &lt;/strong&gt;The study included twenty-four male Wistar albino rats which were divided into four groups. The rats received ethanolic extraction of &lt;em&gt;Rosmarinus officinalis&lt;/em&gt; orally at a dose of 200 mg/kg. Hepatotoxicity was induced orally with a daily dose of 05 mL of 20% alcoholic solution for 90 days. &lt;strong&gt;Results:&lt;/strong&gt; The chemical characterization of the ethanolic extract of&lt;em&gt; Rosmarinus officinalis &lt;/em&gt;(EER) by HPLC/UV shows the presence of polyphenolic compounds and numerous flavonoids, the main constituent of which is rosmarinic acid. It was noticed that the Ethanol caused an increase in liver function parameters (aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, triglyceride and cholesterol, total bilirubin) compared to the control and oxidative stress through a significant decrease in antioxidant liver enzymes Superoxidase dismutase (9.39 U/mg), glutathione peroxidase (12.89 U/mg) and catalase (25.39 U/mg) and increased malondialdehyde levels. The histological study showed significant lesions in the liver. &lt;strong&gt;Conclusion:&lt;/strong&gt; The disturbances in liver function, antioxidant status and structural damage to the liver caused by ethanol have been restored by the administration of the ethanolic extract of&lt;em&gt; Rosmarinus officinalis &lt;/em&gt;which strongly justifies its therapeutic effect.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1205</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Rima Farah AOUAD&lt;sup&gt;1&lt;/sup&gt;, Mokhtaria Yasmina BOUFADI&lt;sup&gt;2,3,&lt;/sup&gt;*, Djallal Eddine Houari ADLI&lt;sup&gt;1&lt;/sup&gt;, Faiza Moulai-Hacene&lt;sup&gt;2&lt;/sup&gt;, Khaled KAHLOULA&lt;sup&gt;1&lt;/sup&gt;, Miloud SLIMANI&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Laboratory of Biotoxicology, Pharmacognosy and Biological Valorisation of plants (LBPVBP). Department of Biology, Faculty of Natural and Life Sciences, Moulay Tahar University, Saida, ALGERIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Laboratory of Bioeconomics, Food Safety and Health, Faculty of Natural Sciences and Life, Université de Abdelhamid Ibn Badis, Mostaganem, ALGERIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Laboratory of Pharmaceutical Chemistry, Faculty of Pharmacy, Université Libre de Bruxelles, Brussels, BELGIUM.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mokhtaria Yasmina BOUFADI</style></author><author><style face="normal" font="default" size="100%">Soumia KEDDARI</style></author><author><style face="normal" font="default" size="100%">Faiza MOULAI-HACENE</style></author><author><style face="normal" font="default" size="100%">Sara CHAA</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chemical Composition, Antioxidant and Anti-Inflammatory Properties of Salvia Officinalis Extract from Algeria</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biomarkers of inflammation</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC/UV</style></keyword><keyword><style  face="normal" font="default" size="100%">Lipoperoxydation</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxydative stress</style></keyword><keyword><style  face="normal" font="default" size="100%">Salvia officinalis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">506-515</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Due to its flavoring and seasoning properties, &lt;em&gt;Salvia officinalis &lt;/em&gt;has been widely used in the preparation of many foods. In folk medicine in Asia and Latin America, it has been used for the treatment of various types of disorders, including seizures, ulcers, rheumatism, inflammation, dizziness, and high blood sugar. &lt;strong&gt;Objective: &lt;/strong&gt;The purpose of this study is to determine the chemical composition by HPLC/UV, antioxidant activity and lipid peroxidation; thus the, the anti-inflammatory effect of the ethanolic extract of &lt;em&gt;Salvia officinalis &lt;/em&gt;(EES) on certain homeostatic parameters, inflammatory biomarkers and antioxidant status in Wistar rats subjected to inflammation induced by carrageenan. &lt;strong&gt;Method:&lt;/strong&gt; Male rats (&lt;em&gt;n&lt;/em&gt; = 24) were exposed to inflammation of the peritoneal by carrageenan (200 μL: 2%) and treated for 5 days with ethanolic extract of &lt;em&gt;Salvia officinalis&lt;/em&gt; (EES) in order to repair the damage caused by inflammation on homeostasis, TNF-α and PGE2. &lt;strong&gt;Results:&lt;/strong&gt; The results of scavenging of DPPH and lipoperoxidation of the extract, showed an IC&lt;sub&gt;50 &lt;/sub&gt;of 29.69 ± 1.32 and 46.17 ± 1.51 μg/mL, respectively. The identification of EEC by HPLC shows the presence of polyphenolic acids (salvianolic acid, rosmarinic acid, caffeic acid, ferulic acid) and many flavonoids (Cirsimaritin, Catechin, Acacetin, kaempferol, pinocembrine, quercetin). Salvia extract contains 221.08 ± 2.36 mg EAG/g and 80.54 ± 1.3 mg EQ/g dry extract. Compared to the control group, carrageenan induced a substantial decrease (P&amp;lt;0.05) in antioxidant enzymes and a highly significant increase (P&amp;lt;0.05) in homeostatic parameters (blood sugar, CRP and fibrinogen), biomarkers of inflammation (TNF-α and PGE2) and malondialdehyde levels. &lt;strong&gt;Conclusion:&lt;/strong&gt; The administration of Salvia extract corrects this perturbation where there is an improvement in antioxidant enzymes and a decrease in biomarkers of inflammation. &lt;em&gt;Salvia officinalis&lt;/em&gt; has been able to repair carrageenin-induced perturbations homeostasis and inflammation markers in Wistar rats.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">506</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Mokhtaria Yasmina BOUFADI&lt;sup&gt;1,2,&lt;/sup&gt;*, Soumia KEDDARI&lt;sup&gt;1&lt;/sup&gt;, Faiza MOULAIHACENE&lt;sup&gt;1&lt;/sup&gt;, Sara CHAA&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Laboratory of Beneficial Microorganisms, Functional Food and Health (LMBAFS). Faculty of Natural Sciences and Life. Abdelhamid Ibn Badis University, Mostaganem, ALGERIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Laboratory of Pharmaceutical Chemistry, Faculty of Pharmacy, Libre University, Brussels, BELGIUM.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sharada L Deore</style></author><author><style face="normal" font="default" size="100%">Shital R Ingole</style></author><author><style face="normal" font="default" size="100%">Bhushan A Baviskar</style></author><author><style face="normal" font="default" size="100%">Anjali A kide</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Pharmacognostical, Phytochemical and Biological Evaluation of Five Ocimum Species</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ocimum americanum</style></keyword><keyword><style  face="normal" font="default" size="100%">Ocimum basilicum</style></keyword><keyword><style  face="normal" font="default" size="100%">Ocimum gratissimum</style></keyword><keyword><style  face="normal" font="default" size="100%">Ocimum kilimandscharicum</style></keyword><keyword><style  face="normal" font="default" size="100%">Ocimum sanctum</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">463-474</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;There are about 150 species of &lt;em&gt;Ocimum&lt;/em&gt; in the world and out of that 68 species are found in India. Comparative pharmacognostic study of these &lt;em&gt;Ocimum&lt;/em&gt; species is unspecified. Growing demand of &lt;em&gt;Ocimum&lt;/em&gt; plants demands quality standards for correct identification of desired &lt;em&gt;Ocimum &lt;/em&gt;species. &lt;strong&gt;Objectives:&lt;/strong&gt; Hence aim of present study is to establish comparative pharmacognostical, phytochemical and biological standards for most commonly found and morphologically confusing five species of &lt;em&gt;Ocimum&lt;/em&gt;. &lt;strong&gt;Methods:&lt;/strong&gt; Macroscopic, microscopic, preliminary phytochemical evaluations, extraction of essential oils, TLC analysis, &lt;em&gt;in vitro&lt;/em&gt; antioxidant and antimicrobial potency of selected five species carried out and compared. &lt;strong&gt;Results:&lt;/strong&gt; This comparative study reports that &lt;em&gt;O. sanctum&lt;/em&gt; should be preferred in medicine use among selected five species based on phytochemical composition, antioxidant and antimicrobial potency.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">463</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sharada L Deore*, Shital R. Ingole, Bhushan A Baviskar, Anjali A. kide&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Govt. College of Pharmacy, Amravati-444 604, Maharashtra, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Akanksha Mittal</style></author><author><style face="normal" font="default" size="100%">Sunil Tejaswi</style></author><author><style face="normal" font="default" size="100%">Mruthunjaya K</style></author><author><style face="normal" font="default" size="100%">Suneeth Shetty</style></author><author><style face="normal" font="default" size="100%">Ambikathanaya UK</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparison of Antibacterial Activity of Calcium Hydroxide, Azadirachta Indica (Neem), Ocimum Tenuiflorum (Tulsi) and Punica Granatum (Pomegranate) Gels as Intracanal Medicaments Against Enterococcus Faecalis: An in-vitro Study</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Calcium hydroxide</style></keyword><keyword><style  face="normal" font="default" size="100%">Enterococcus faecalis</style></keyword><keyword><style  face="normal" font="default" size="100%">Herbal</style></keyword><keyword><style  face="normal" font="default" size="100%">Intracanal medicaments</style></keyword><keyword><style  face="normal" font="default" size="100%">Microbial sensitivity tests</style></keyword><keyword><style  face="normal" font="default" size="100%">Root canal therapy</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2017</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">988-994</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Aim: &lt;/strong&gt;This study aimed to evaluate the antibacterial activity of Calcium hydroxide, Azadirachta indica (Neem), Ocimum tenuiflorum (Tulsi) and Punica granatum (Pomegranate) gels as intracanal medicaments against &lt;em&gt;Enterococcus faecalis&lt;/em&gt;. &lt;strong&gt;Methodology:&lt;/strong&gt; Crude extracts of Pomegranate peel, Neem leaves and Tulsi leaves were used to determine MIC following which gels of 5% neem, 10% tulsi and 10% pomegranate were prepared. Forty-eight single rooted human premolars were procured and inoculated with E.faecalis for 7 days. Specimens were then randomly distributed into 4 groups.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Group I- Calcium hydroxide&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Group II- 5% A. indica (Neem) gel&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Group III- 10% O. tenuiflorum (Tulsi) gel&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Group IV-10%&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;P. granatum (Pomegranate) gel The experimental gels were then introduced into the samples and were sealed at both ends. The antimicrobial activity of medicaments was assessed by measuring CFU/ml at the end of 1, 3 and 5 days. &lt;strong&gt;Results:&lt;/strong&gt; Calcium hydroxide showed the maximum antibacterial activity (5.3X10&lt;sup&gt;4 &lt;/sup&gt;CFU/ml) followed by Pomegranate gel (5.4 X10&lt;sup&gt;4&lt;/sup&gt; CFU/ml) with no statistically significant difference between them. Similarly, no statistically significant difference was observed between the mean CFU/ml values of the neem (10.2 X10&lt;sup&gt;4 &lt;/sup&gt;CFU/ml) and tulsi gel (10.2 X10&lt;sup&gt;4&lt;/sup&gt; CFU/ml). However, pomegranate gel showed statistically significant antibacterial activity when compared to Neem and Tulsi. (Table 1, Table 2, Table 3, table 4) (Figure 1). &lt;strong&gt;Conclusion:&lt;/strong&gt; Calcium hydroxide showed the best antibacterial activity against E.faecalis. Among herbal gels, pomegranate showed the maximum antibacterial activity, however, further &lt;em&gt;in-vivo&lt;/em&gt; research is required for it to be used as a sole intracanal medicament clinically.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">988</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Akanksha Mittal, Sunil Tejaswi*, Mruthunjaya K, Suneeth Shetty, Ambikathanaya UK&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;JSS Dental College and Hospital, Mysuru, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Soumia KEDDARI</style></author><author><style face="normal" font="default" size="100%">Mokhtaria Yasmina BOUFADI</style></author><author><style face="normal" font="default" size="100%">Meriem MOKHTAR</style></author><author><style face="normal" font="default" size="100%">Djahira HAMED</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Culture of Lactic Acid Bacteria in Natural Environments Based on Dates</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Dates</style></keyword><keyword><style  face="normal" font="default" size="100%">Fermentation</style></keyword><keyword><style  face="normal" font="default" size="100%">Lactic acid bacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">Medium</style></keyword><keyword><style  face="normal" font="default" size="100%">MRS</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">675-681</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Lactic acid bacteria are used in the food industry and have restrictive criteria for probiotic potential. The most common growth media used for lactic acid bacteria is de Man, Rogosa, and Sharpe culture medium (MRS). &lt;strong&gt;Methods: &lt;/strong&gt;In this study, three culture media were developed (date powder DP, date core DC and date core associated with lentils CL) based on locally available plant materials with a low market value to obtain a less expensive culture medium compared to the reference medium MRS for the growth of lactic acid bacteria. Four lactic strains were used (&lt;em&gt;Lactobacillus acidophilus&lt;/em&gt; LbA-CECT4529, &lt;em&gt;Lactobacillus plantarum &lt;/em&gt;LbP-CECT 748, &lt;em&gt;Bifidobacterium animalis &lt;/em&gt;subsp lactis Bb12 and &lt;em&gt;Bifidobacterium bifidum &lt;/em&gt;Bb 443). The growth and acidification kinetics of the tested strains were evaluated. The content sugar was determinate with HPLC.&lt;strong&gt; Results: &lt;/strong&gt;All lactic bacteria were able to grow on all culture media, but the best results were obtained with MRS and DP media. No significant difference (&lt;em&gt;p&lt;/em&gt; &amp;lt;0.05) was observed between DP and MRS medium. The consumption of sugars and proteins in the DP medium was good with all tested bacteria (70.87 to 81.96% and 71.42 to 80.90%, respectively). After the analysis of sugar content of DP medium before and after fermentation with high-performance liquid chromatography (HPLC), fructose was the only sugar detected (45.28μg/ml ± 0.24). After fermentation, 83% of fructose was consumed by Bb12. &lt;strong&gt;Conclusion: &lt;/strong&gt;The present data allow us to conclude that date medium promotes the growth of lactic bacteria and can be considered as MRS standard medium substitute.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">675</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Soumia KEDDARI&lt;sup&gt;1,&lt;/sup&gt;*, Mokhtaria Yasmina BOUFADI&lt;sup&gt;1&lt;/sup&gt;, Meriem MOKHTAR&lt;sup&gt;1&lt;/sup&gt;, Djahira HAMED&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Laboratory of Beneficial Microorganisms, Functional Foodand Health (LMBAFS), Faculty of Natural Sciences and Life. Abdelhamid Ibn Badis University, Mostaganem, ALGERIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nur Haseena Kajahmohideen</style></author><author><style face="normal" font="default" size="100%">Siti NurSyafiqah Razi</style></author><author><style face="normal" font="default" size="100%">Ghasak Ghazi Faisal</style></author><author><style face="normal" font="default" size="100%">Abdelkader Elbadawy Ashour</style></author><author><style face="normal" font="default" size="100%">Anisa Kusumawardani</style></author><author><style face="normal" font="default" size="100%">Essam A. Makky</style></author><author><style face="normal" font="default" size="100%">OE Ibrahim</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cytotoxic Activity of Eurycoma Longifolia Jack Root Extract Against Nasopharyngeal Carcinoma Cell Line</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cytotoxic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">E. longifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">Nasopharyngeal carcinoma</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1014-1018</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Eurycoma longifolia &lt;/em&gt;(&lt;em&gt;E. longifolia&lt;/em&gt;) or Tongkat Ali is a tree that grows in southeast Asia, the roots of which contain bioactive components that exhibit cytotoxic properties against various cancer cell lines. However, no study has been conducted to relate the cytotoxic properties against nasopharyngeal carcinoma (NPC), a type of cancer that shows poor prognosis for metastatic disease. The purpose of this study was to determine whether the &lt;em&gt;E. longifolia&lt;/em&gt; root extract exerts cytotoxic activity against nasopharyngeal carcinoma (ORL-115) cell lines. &lt;strong&gt;Materials and Method: &lt;/strong&gt;&lt;em&gt;E. longifolia&lt;/em&gt; root extracts were obtained through Soxhlet extraction method and by using two different solvents; ethanol and dicholoromethane. MTS assay was used to evaluate the cytotoxic effect of the root extracts against ORL-115 cell line for three different incubation time which were 24-hour, 48-hour and 72-hour. &lt;strong&gt;Results: &lt;/strong&gt;Ethanol extract was significantly more potent compared to DCM extract. Ethanol extract exhibited lower IC&lt;sub&gt;50&lt;/sub&gt; value compared to DCM extract. The IC&lt;sub&gt;50 &lt;/sub&gt;of ethanol extract were 232.1 μg/ml, 66.86 μg/ml and 42.6 μg/ml. Meanwhile the IC&lt;sub&gt;50&lt;/sub&gt; of DCM extract were 678.87 μg/ml, 136.71 μg/ml, 73.72 μg/ml for 24-hour, 48-hour and 72-hour incubation period respectively. The cytotoxic activity of both extracts increased as the incubation time prolonged. The cytotoxic activity of ethanol extract at each incubation time was significantly different from DCM extract except at 72 hours. &lt;strong&gt;Conclusion:&lt;/strong&gt; &lt;em&gt;E. longifolia&lt;/em&gt; root extracts exerted cytotoxic activity against the nasopharyngeal carcinoma (ORL-115) cell line. Ethanol extract exhibited lower IC&lt;sub&gt;50&lt;/sub&gt; value compared to DCM extract. The cytotoxic activity of both extracts were dose dependent and time dependent.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1014</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nur Haseena Kajahmohideen&lt;sup&gt;1&lt;/sup&gt;, Siti NurSyafiqah Razi&lt;sup&gt;1&lt;/sup&gt;, Ghasak Ghazi Faisal&lt;sup&gt;2,&lt;/sup&gt;*, Abdelkader Elbadawy Ashour&lt;sup&gt;3&lt;/sup&gt;, Anisa Kusumawardani&lt;sup&gt;4&lt;/sup&gt;, Essam A. Makky&lt;sup&gt;5&lt;/sup&gt;, O.E. Ibrahim&lt;sup&gt;6&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Kulliyyah of Dentistry, IIUM, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Lecturer, Department of fundamental dental and medical sciences, Kulliyyah of Dentistry, IIUM, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Lecturer, Basic Medical Science Unit, Kulliyyah of Medicine, IIUM, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Restorative Dentistry, Kuliyyah of Dentistry, IIUM, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Faculty of Industrial Sciences &amp;amp; Technology, Universiti Malaysia Pahang (UMP), Gambang, 26300 Kuantan, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Faculty of Dentistry, Universiti Teknologi MARA, MALAYSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Urarat Nanna</style></author><author><style face="normal" font="default" size="100%">Linda Chularojmontri</style></author><author><style face="normal" font="default" size="100%">Pholawat Tingpej</style></author><author><style face="normal" font="default" size="100%">Rawiwun Kaewamatawong</style></author><author><style face="normal" font="default" size="100%">Sudarat Homhual</style></author><author><style face="normal" font="default" size="100%">Wanwisa Suwannaloet</style></author><author><style face="normal" font="default" size="100%">Thanes Fuangfoo</style></author><author><style face="normal" font="default" size="100%">Jarinyaporn Naowaboot</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Aporosa villosa Stem Ethanolic Extract on Adipogenesis in 3T3-L1 Adipocytes</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Aporosa villosa; Adipogenesis; Obesity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1422-1427</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background&lt;/strong&gt;: An excessive fat accumulation is related to development of obesity. Obesity is associated with the induction of insulin resistance and diabetes mellitus conditions. &lt;em&gt;Aporosa villosa &lt;/em&gt;is a plant that found in the Northern and Northeastern region of Thailand.&lt;strong&gt; Objective: &lt;/strong&gt;The present study used 3T3-L1 adipocytes for investigating the effect of &lt;em&gt;Aporosa villosa&lt;/em&gt; stem ethanolic extract (AS) on adipogenesis. &lt;strong&gt;Materials and Methods&lt;/strong&gt;: 3T3-L1 adipocytes were used for measuring the cytotoxicity of AS at a concentration range of 3-100 μg/mL. After adipocyte cells treated with AS (3-100 μg/mL) for 8 days, the lipid accumulation was detected by Oil Red O staining and adipogenic gene expression were determined by quantitative real-time PCR. &lt;strong&gt;Results: &lt;/strong&gt;AS extracts (3-100 μg/mL) did not show cytotoxicity on cell proliferation. After 8 days of treating 3T3-L1 adipocytes with AS at doses of 3, 10, 30 and 100 μg/mL, the lipid droplets were reduced as compared to non-treated cells. Furthermore, the adipogenic genes were measured. The regulators of adipogenesis, CCAAT/enhancer-binding protein α (C/EBPα), peroxisome proliferatoractivated receptor γ (PPARγ) and sterol regulatory element binding protein 1c (SREBP1c) were found decreasing in AS extracts. The downstream target genes of these regulators cluster of differentiation (CD) 36, fatty acid synthase (FAS) and lipoprotein lipase (LPL) were also reduced by AS treatments. &lt;strong&gt;Conclusion:&lt;/strong&gt; These findings indicate that AS extract has an inhibitory activity on adipogenesis in 3T3-L1 adipocytes via suppressing C/EBPα, PPARγ and SREBP1c.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1422</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Urarat Nanna&lt;sup&gt;1&lt;/sup&gt;, Linda Chularojmontri&lt;sup&gt;1&lt;/sup&gt;, Pholawat Tingpej&lt;sup&gt;1&lt;/sup&gt;, Rawiwun Kaewamatawong&lt;sup&gt;2&lt;/sup&gt;, Sudarat Homhual&lt;sup&gt;2&lt;/sup&gt;, Wanwisa Suwannaloet&lt;sup&gt;3&lt;/sup&gt;, Thanes Fuangfoo&lt;sup&gt;4 &lt;/sup&gt;&amp;nbsp;Jarinyaporn Naowaboot&lt;sup&gt;1,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Preclinical Science, Faculty of Medicine, Thammasat University, Pathum Thani 12120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Pharmaceutical Sciences, Ubon Ratchathani University, Ubon Ratchathani, 34190, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Medicine, Ubon Ratchathani University, Ubon Ratchathani, 34190, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacology, College of Pharmacy, Rangsit University, Pathum Thani 12120, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Muhamad Iyad bin Ramzi</style></author><author><style face="normal" font="default" size="100%">Muhammad Hazzim bin Kosnin</style></author><author><style face="normal" font="default" size="100%">Ghasak Ghazi Faisal</style></author><author><style face="normal" font="default" size="100%">Mohd Hafiz Arzmi</style></author><author><style face="normal" font="default" size="100%">Anisa Kusumawardani</style></author><author><style face="normal" font="default" size="100%">ASM Sabere</style></author><author><style face="normal" font="default" size="100%">Essam A Makky</style></author><author><style face="normal" font="default" size="100%">OE Ibrahim</style></author><author><style face="normal" font="default" size="100%">Ghasak Ghazi Faisal</style></author><author><style face="normal" font="default" size="100%">Mohd Hafiz Arzmi</style></author><author><style face="normal" font="default" size="100%">Anisa Kusumawardani</style></author><author><style face="normal" font="default" size="100%">ASM Sabere</style></author><author><style face="normal" font="default" size="100%">Essam A Makky</style></author><author><style face="normal" font="default" size="100%">OE Ibrahim</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Eurycoma Longifolia Jack (Tongkat Ali) Root Extract on salivary S. Mutans, Lactobacillus and Candida Albicans Isolated from High-Risk Caries Adult Patients</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimicrobial effect</style></keyword><keyword><style  face="normal" font="default" size="100%">Eurycoma longifolia Jack</style></keyword><keyword><style  face="normal" font="default" size="100%">Inhibition</style></keyword><keyword><style  face="normal" font="default" size="100%">Salivary isolate</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">787-791</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Introduction: The roots of &lt;em&gt;E. longifolia jack&lt;/em&gt; (E.L.) or Tongkat Ali have been used in traditional medicine as well as supplements and food additives. Many chemical compounds have been detected in extracts of its roots which are believed to be responsible for its medicinal properties. In this study, our objectives were to study the effects of EL root extracts on the growth of &lt;em&gt;Streptococcus Mutans, Lactobacillus&lt;/em&gt; and &lt;em&gt;Candida Albicans &lt;/em&gt;isolated from saliva of adult patients with high caries risk. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;The ethanolic extract of the root of this plant was tested against saliva isolated &lt;em&gt;Streptococcus Mutans, Lactobacillus&lt;/em&gt; and&lt;em&gt; Candida Albicans&lt;/em&gt; via disc diffusion assay at a concentration of 200mg/mL. The minimum inhibitory concentration was carried out by the standard broth microdilution method. Cell viability of test microorganisms against different concentration of the extract and inhibition zones were calculated.&lt;strong&gt; Results:&lt;/strong&gt; Disk diffusion assay showed positive zones of inhibition for all test microorganisms with &lt;em&gt;S. mutans, Lactobacillus &lt;/em&gt;and &lt;em&gt;C. albicans&lt;/em&gt; exhibiting zones of inhibition of 8.3 ± 0.7mm, 12.4 ± 2.4mm and 21.4 ± 2.7mm respectively. For minimum inhibitory concentration, the test microorganisms were tested at concentration of 250mg/ mL, 125mg/mL, 62.5mg/mL, 31.3mg/mL and 0mg/mL. The minimum inhibitory concentration showed that MIC of S. mutans was at 62.5mg/mL, Lactobacillus at 125mg/mL and C. albicans at 31.3mg/mL. Lastly, the cell viability results supported the MIC determined prior. &lt;strong&gt;Conclusion:&lt;/strong&gt; Ethanol-based &lt;em&gt;E.&lt;/em&gt; &lt;em&gt;longifolia Jack&lt;/em&gt; root extract has an antimicrobial effect on the following microorganisms isolated from the saliva of high-risk caries adult patients: &lt;em&gt;S. mutans, Lactobacillus&lt;/em&gt; and &lt;em&gt;C. albicans.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">787</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Muhamad Iyad bin Ramzi1, Muhammad Hazzim bin Kosnin&lt;sup&gt;1&lt;/sup&gt;, Ghasak Ghazi Faisal&lt;sup&gt;2,&lt;/sup&gt;*, Mohd Hafiz Arzmi&lt;sup&gt;2&lt;/sup&gt;, Anisa Kusumawardani&lt;sup&gt;3&lt;/sup&gt;, ASM Sabere&lt;sup&gt;4&lt;/sup&gt;, Essam A. Makky&lt;sup&gt;5&lt;/sup&gt;, O.E. Ibrahim&lt;sup&gt;6&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Kuliyyah of Dentistry, International Islamic University Malaysia (IIUM), MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Fundamental Dental and Medical Sciences, Kuliyyah of Dentistry, IIUM, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Restorative Dentistry, Kuliyyah of Dentistry, IIUM, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Kulliyyah of Pharmacy, International Islamic University, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Faculty of Industrial Sciences &amp;amp; Technology, Universiti Malaysia Pahang (UMP), Gambang, 26300 Kuantan, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Faculty of Dentistry, Universiti Teknologi MARA, MALAYSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Natasha Yemima Situmorang</style></author><author><style face="normal" font="default" size="100%">Endah Zuraidah</style></author><author><style face="normal" font="default" size="100%">Ari Estuningtyas</style></author><author><style face="normal" font="default" size="100%">Aryo Tedjo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Mahkota Dewa (Phaleria macrocarpa) Leaf Extract on the Mucin 1 Expression in Mice Colonic Epithelial Cells Induced by Dextran Sodium Sulfate (DSS)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory agent</style></keyword><keyword><style  face="normal" font="default" size="100%">Colon epithelial cell</style></keyword><keyword><style  face="normal" font="default" size="100%">Inflammatory bowel Disease</style></keyword><keyword><style  face="normal" font="default" size="100%">Mahkota Dewa (Phaleria macrocarpa)</style></keyword><keyword><style  face="normal" font="default" size="100%">MUC 1 expression</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1509-1515</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Inflammatory bowel disease is a chronic inflammation caused by the malignant inflammation response and if not treated, could lead to colorectal cancer. One of the researched treatment is mahkota dewa (&lt;em&gt;Phaleria macrocarpa&lt;/em&gt;) leaf extract that has flavonoid compound known to reduce inflammation. This study was aimed to prove that mahkota dewa leaf extract could reduce inflammation of mice colon induced with dextran sodium sulfate (DSS) and observe MUC1 expression from colon epithelial crypt of Lieberkuhn. &lt;strong&gt;Methods&lt;/strong&gt;: This was a laboratory experiment using biological material (paraffin block) taken from 28 mice and divided into 5 groups: normal, aspirin, low and high dose mahkota dewa, and negative control. They were processed into immunohistochemistry and stained microscopic slides. Afterwards, they were observed with 400x magnification and 5 field-of-view of mice colon crypt of lieberkuhn. Then MUC1 expression was counted using ImageJ to obtain mean immunohistochemistry score and analyzed with SPSS. &lt;strong&gt;Results:&lt;/strong&gt; There were significant reduction of MUC1 expressions from normal, aspirin, and high dose mahkota dewa groups compared to the negative control group. The result shown MUC1 expression from high dose mahkota dewa (M=149.90,SD=3.81) and aspirin (M=158.92,SD=5.28) were closer to normal group (M=148.02,SD=5.28). There were no significant results between negative (M=175.39,SD=14.30) and low dose mahkota dewa group (M=149.90,SD=5.02).&lt;strong&gt; Conclusion:&lt;/strong&gt; There was a reduction of MUC1 expression in DSS-induced mice colonic epithelial cells for high dose mahkota dewa group. This shown that high dosage mahkota dewa leaf extract could reduce inflammation like aspirin.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1509</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kusmardi Kusmardi&lt;sup&gt;1-3,*&lt;/sup&gt;, Natasha Yemima Situmorang&lt;sup&gt;4&lt;/sup&gt;, Endah Zuraidah&lt;sup&gt;5&lt;/sup&gt;, Ari Estuningtyas&lt;sup&gt;6&lt;/sup&gt;, Aryo Tedjo&lt;sup&gt;2,7&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anatomic Pathology, Faculty of Medicine – Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Drug Development Research Center, Indonesia Medical Education and Resesarch Institute (IMERI), Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Human Cancer Research Center, IMERI, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Anatomic Pathology, Faculty of Medicine – Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Pharmacology and Therapeutic, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Department of Medical Chemistry, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Baiqi Nur Hairi</style></author><author><style face="normal" font="default" size="100%">Nadar Sukri Lubis</style></author><author><style face="normal" font="default" size="100%">Tri Wahyuni Lestari</style></author><author><style face="normal" font="default" size="100%">Putri Reno Intan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Sambiloto and Spirulina Combination on Mucin-1 Protein Expression in Medial Colon of Plasmodium berghei ANKA Infected Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Medial colon</style></keyword><keyword><style  face="normal" font="default" size="100%">Muc-1</style></keyword><keyword><style  face="normal" font="default" size="100%">Plasmodium berghei Anka</style></keyword><keyword><style  face="normal" font="default" size="100%">Sambiloto</style></keyword><keyword><style  face="normal" font="default" size="100%">Spirulina</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1359-1365</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Malaria still be health problem in the world, especially in Eastern Indonesia. Malaria’s inflammation and metabolism defect can cause colonic damage, such as enhancement Muc-1 protein expression and goblet cells hyperplasia. Sambiloto and spirulina combination as antiinflammatory and antioxidative agent can prevent medial colon damage &lt;em&gt;Plasmodium berghei &lt;/em&gt;ANKA infected mice. The aim of the study to show the effect of sambiloto and spirulina combination on Muc-1 protein activity in medial colon &lt;em&gt;Plasmodium berghei&lt;/em&gt; ANKA infected mice. This study use preserve male Swiss Webser mice colonic tissue which has inoculated by&lt;em&gt; Plasmodium berghei &lt;/em&gt;ANKA, whose treatment group include positive control (dehyroartemisin piperaquine), negative control (carboxymethil cellulose), AP (sambiloto), AP+ES (sambiloto+spirulina extract), and AP+PS (sambiloto+spirulina powder) and terminated after 28 days of treatment. Colonic tissue was stained with immunohistochemistry and observed using light microscope (400x) in five different field and was analyzed with ImageJ® sowtware, and statisitcal analysis was done with SPSS 20.0. According to One Way ANOVA and Duncan posthoc test, only AP+PS(120,98 ±3,37), which significantly difference between negative control, AP, and AP+ES group. Meanwhile, between DHP, AP+PS group not significantly differenece. Sambiloto extract and spirulina powder combination can reduce Muc-1 protein expression in medial colon &lt;em&gt;Plasmodium berghei &lt;/em&gt;ANKA infected mice.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1359</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kusmardi Kusmardi&lt;sup&gt;1-4&lt;/sup&gt;,*, Baiqi Nur Hairi&lt;sup&gt;5&lt;/sup&gt;, Nadar Sukri Lubis&lt;sup&gt;6&lt;/sup&gt;, Tri Wahyuni Lestari&lt;sup&gt;7&lt;/sup&gt;, Putri Reno Intan&lt;sup&gt;8&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Anatomical Pathology Department, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Drug Development Research Cluster, Indonesia Medical Educational and Research Institute, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Human Cancer Research Cluster, Indonesia Medical Educational and Research Institute, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Doctoral Program in Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Undergraduate Program, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Parasitology Department, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;National Institute of Health Research and Development, Ministry of Health of Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Centre for Research and Development of Biomedical and Basic Health Technology, National Institute of Health Research and Development, Ministry of Health, Jakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tanti Azizah Sujono</style></author><author><style face="normal" font="default" size="100%">Ika Trisharyanti Dian Kusumowati</style></author><author><style face="normal" font="default" size="100%">Rima Munawaroh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of Jamaican cherry (Muntingia calabura L.) Fruits Extract on Immunoglobulin G Levels and Hematological Profiles in Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hematological profile</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatitis B vaccine</style></keyword><keyword><style  face="normal" font="default" size="100%">Immunoglobulin G</style></keyword><keyword><style  face="normal" font="default" size="100%">Jamaican cherry (Muntingia calabura L.)</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">535-541</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Jamaican cherry (&lt;em&gt;Muntingia calabura&lt;/em&gt; L.) fruits contain potential immunomodulatory agents such as phenolic and flavonoid compounds. However, previous research was limited only to the effect of Jamaican cherry fruits on non-specific immune response namely the phagocytic index. &lt;strong&gt;Objective:&lt;/strong&gt; This study aims to determine the immunomodulatory activity of Jamaican cherry fruits against specific immune response by measuring the antibody formation named immunoglobulin G (IgG). In addition, the hematological profile of the animals induced by hepatitis B vaccine was also evaluated. &lt;strong&gt;Materials and methods: &lt;/strong&gt;forty male mice were grouped into 8 groups consist of control, treatment, and standard groups. Control group was given CMC-Na 0.5%, six treatment groups were each given either the methanol extract of Jamaican cherry fruits (MEJF), or ethyl acetate fraction of Jamaican cherry fruits (EAJFJ) with the doses of 50, 100, and 200 mg/kg BW (each dose for one group), and levamisole was given to the standard group. Levamisole and extract of Jamaican cherry fruits were prepared as a suspension in CMCNa 0.5% and administered orally for 15 days. Mice were induced with hepatitis B vaccine intraperitoneally twice. The levels of IgG, hematological profiles, and organ index were measured on the 16&lt;sup&gt;th&lt;/sup&gt; day. &lt;strong&gt;Results:&lt;/strong&gt; The administration of MEJF and EAFJF stimulated IgG production significantly compared to the control group (p&amp;lt;0.05). Meanwhile, the MEJF and EAFJF did not influence the hematological profile. An increase of the spleen index was found in the EAFJF group compared to the control. Both MEJF and EAFJF were shown to have flavonoids, phenolics, and triterpenoids contents. &lt;strong&gt;Conclusion: &lt;/strong&gt;MEJF and EAFJF possessed immunostimulant properties by increasing the specific (humoral) immune response (IgG) after induction with the hepatitis B vaccine.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">535</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Tanti Azizah Sujono&lt;sup&gt;1,&lt;/sup&gt;*, Ika Trisharyanti Dian Kusumowati&lt;sup&gt;2&lt;/sup&gt;, Rima Munawaroh&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology and Clinical Pharmacy, Faculty of Pharmacy, Universitas Muhammadiyah Surakarta, 57162, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Universitas Muhammadiyah Surakarta, 57162, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biology Pharmacy, Faculty of Pharmacy, Universitas Muhammadiyah Surakarta, 57162, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Neeraj Choudhary</style></author><author><style face="normal" font="default" size="100%">Pranav Kumar Prabhakar</style></author><author><style face="normal" font="default" size="100%">Gopal L Khatik</style></author><author><style face="normal" font="default" size="100%">Subba Rao Chamakuri</style></author><author><style face="normal" font="default" size="100%">Devesh Tewari</style></author><author><style face="normal" font="default" size="100%">Ashish Suttee</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Acute toxicity, In-vitro, In-vivo Antidiabetic Potential of the Flavonoid Fraction of the plant Chenopodium album L</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acute toxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Alpha-amylase</style></keyword><keyword><style  face="normal" font="default" size="100%">Antidiabetic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Chenopodium album</style></keyword><keyword><style  face="normal" font="default" size="100%">Lc-Ms</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">765-779</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;The &lt;em&gt;Chenopodium album &lt;/em&gt;L. commonly recognized as Bathua, is widely distributed globally and contains various phytoconstituents that help treat several diseases. However, until now, aerial parts' antidiabetic potential and the plant's acute toxicity at fraction level have never been established. &lt;strong&gt;Objectives: &lt;/strong&gt;To investigate the acute toxicity, the&lt;em&gt; in-vitro&lt;/em&gt;,&lt;em&gt; in-vivo&lt;/em&gt; antidiabetic potential of the plant at fraction level. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;The aerial parts of the plant were fractionated into different fractions, i.e., flavonoid fraction (CAFF), tannin fraction (CATF), alkaloid fraction (CAAF), saponin fraction (CASF), and were analyzed for&lt;em&gt; in-vitro &lt;/em&gt;alpha-amylase inhibition assay. The CAFF, CATF, and CAAF were selected based on&lt;em&gt; in-vitro &lt;/em&gt;alpha-amylase inhibition assay results and were further screened for its acute toxicity and&lt;em&gt; in vivo &lt;/em&gt;antidiabetic activity using a high-fat diet and streptozotocin-induced diabetes model. The CAFF was characterized by LC-MS, and a molecular docking study was carried out. &lt;strong&gt;Results:&lt;/strong&gt; The &lt;em&gt;in-vitro &lt;/em&gt;alpha-amylase inhibition assay revealed that CAFF was found to be more potent than standard Acarbose having IC&lt;sub&gt;50&lt;/sub&gt; values 122.18 ± 1.15 and 812.83± 1.07 μg/ml, respectively. The CAFF fraction was found to possess potent antidiabetic activity in a dose-dependent manner in both in vitro and &lt;em&gt;in vivo &lt;/em&gt;diabetic models and did not produce any sign of severe toxicity. Furthermore, the bioactive CAFF fraction was characterized by LC-MS, showed the presence of quercetin 3-O-(2’’,6’’-di-O-rhamnosyl) glucoside (QRG) or quercetin 3-O-(2’’,6’’-di-Orhamnosyl) galactoside (QRGa) and quercetin 3-O-rutinoside (rutin) (QR). It is predicted from the molecular docking study that the CAFF fraction primarily acts as an alphaamylase inhibitor. &lt;strong&gt;Conclusion:&lt;/strong&gt; The CAFF fraction was found to poses dose-dependent potent antidiabetic activity and did not produce any sign of severe toxicity and primarily act as an alpha-amylase inhibitor.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">765</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Neeraj Choudhary&lt;sup&gt;1,2&lt;/sup&gt;, Pranav Kumar Prabhakar&lt;sup&gt;1&lt;/sup&gt;, Gopal L. Khatik&lt;sup&gt;1&lt;/sup&gt;, Subba Rao Chamakuri&lt;sup&gt;1&lt;/sup&gt;, Devesh Tewari&lt;sup&gt;1&lt;/sup&gt;, Ashish Suttee&lt;sup&gt;1,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;School of Pharmaceutical Sciences, Lovely Professional University, Punjab, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Pharmaceutical Sciences, PCTE Group of Institutes, Ludhiana, Punjab, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Asmaa Sayed Abd Elkarim</style></author><author><style face="normal" font="default" size="100%">Amal H. Ahmed</style></author><author><style face="normal" font="default" size="100%">Abdelbaset M. Elgamal</style></author><author><style face="normal" font="default" size="100%">Radwan El Haggar</style></author><author><style face="normal" font="default" size="100%">Alaa Khedr</style></author><author><style face="normal" font="default" size="100%">Mohamed Fouad Shalaby</style></author><author><style face="normal" font="default" size="100%">Roula Bayram</style></author><author><style face="normal" font="default" size="100%">Samah Shabana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evidence Based Evaluation of Pharmacological Activity and Herb-Herb interaction of Organic Extracts of Certain Natural Anti- Diabetic Mixtures</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-diabetic herbs</style></keyword><keyword><style  face="normal" font="default" size="100%">Herb-herb interaction</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal Plants.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1366-1376</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective: &lt;/strong&gt;This work aims to find a new treatment based on the development of safe natural anti-diabetic mixtures. It assesses the hypoglycemic activity of natural mixtures and determines whether there are any negative side effects from the interaction of the herbs and the herbs. &lt;strong&gt;Methods:&lt;/strong&gt; Six natural mixtures were tested for anti-diabetic activity, which was confirmed by a pathological histological examination. We performed a GC-MS analysis on active mixtures 1 and 2, yielding 54 and 38 compounds, respectively. The major compounds were Gingerol, Butan-2-one and 4-(3-hydroxy-2-methoxyphenyl) (97 and 64.02 per cent). &lt;strong&gt;Results: &lt;/strong&gt;Among the six samples, the organic extract of mixture 1 and 2 showed a significant reduction in BGL compared to the standard drug glimepiride at a dose of 10 mg/kg ip and demonstrated a beneficial effect on renal function in alloxan-induced diabetic mice. These results were confirmed by a histopathological study which revealed that both mixture 1 and mixture 2 had decreased morphological and ultrastructural changes in the triggered liver. Docking of cuminaldehyde, Gingerol and α-Copaenin at the active site of human pancreatic enzymes α-amylase and aldol reductase revealed that these compounds had binding affinity at the active site of the enzymes. &lt;strong&gt;Conclusion: &lt;/strong&gt;Our results revealed the anti-diabetic activity of non-polar mixtures consisting of long chain hydrocarbons, oils and non-polar components, thus suggesting that the herbal formulation is safe and effective for the treatment and complication of type 2 diabetes.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1366</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Asmaa Sayed Abd Elkarim&lt;sup&gt;1,*&lt;/sup&gt;, Amal H. Ahmed&lt;sup&gt;2,&lt;/sup&gt; Abdelbaset M. Elgamal&lt;sup&gt;3&lt;/sup&gt;, Radwan El Haggar&lt;sup&gt;4&lt;/sup&gt;, Alaa Khedr&lt;sup&gt;5&lt;/sup&gt;, Mohamed Fouad Shalaby&lt;sup&gt;5&lt;/sup&gt;, Roula Bayram&lt;sup&gt;5&lt;/sup&gt;, Samah Shabana&lt;sup&gt;5&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Chemistry of Tanning Materials and Leather Technology Department, National Research Centre, 33 El Bohouthst. (former EL Tahrirst.)- Dokki-Giza, EGYPT.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacognosy Department, Faculty of Pharmacy, Al-azhar University, 11884 Nasr City, Cairo, EGYPT.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Chemistry of Natural and Microbial Products Department, National Research Centre, 33 El Bohouth st. (former EL Tahrir st.)-Dokki- Giza-EGYPT.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Pharmaceutical Chemistry Department, Faculty of Pharmacy, Helwan University, Cairo 11795, EGYPT.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;5&lt;/sup&gt;Department of pharmacognosy, Faculty of Pharmaceutical Sciences and Drug Manufacturing, Misr University for Science and Technology, MUST, 6th October City, EGYPT.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nur Alisa Kamarudin</style></author><author><style face="normal" font="default" size="100%">Norhazilah Muhamad</style></author><author><style face="normal" font="default" size="100%">Nik Nur Hakimah Nik Salleh</style></author><author><style face="normal" font="default" size="100%">Suat Cheng Tan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Impact of Solvent Selection on Phytochemical Content, Recovery of Tannin and Antioxidant Activity of Quercus Infectoria Galls</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Gallotannin</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus infectoria (QI) galls</style></keyword><keyword><style  face="normal" font="default" size="100%">Tannin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1195-1204</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;&lt;em&gt;Quercus infectoria &lt;/em&gt;(QI) is medicinal plant well known to exhibit enormous therapeutic values. The main medicinal part of QI plant exists in its edible nutritious gall. This study aimed to determine the effects of extraction solvents on the overall phytochemical content, recovery of tannin and antioxidant activity of the QI galls. &lt;strong&gt;Methods: &lt;/strong&gt;Two solvents of different polarity namely water and methanol, were used to extract bioactive compounds from the QI galls using soxhlet extraction technique. Phytochemical, TLC and HPLC assays were performed to detect and quantify the extracted compounds. DPPH assay was conducted to evaluate the antioxidant potential of the extracted compounds. &lt;strong&gt;Results:&lt;/strong&gt; After 6 hours of extraction at respective solvent boiling points, methanol solvent successfully generated 1.8-fold higher crude yield (34.0%) compared to water solvent (18.9%). Phytochemical analysis revealed that both solvent extracts contained different secondary metabolites. The methanol extract was found richer in flavonoid, while the aqueous extract was found richer in phenol, tannin, gallotannin, triterpene and cardiac glycosides. Interestingly, we found that the major type of tannin presence in QI galls was gallotannin (hydrolysable tannin) instead of phlobatannin (non-hydrolysable tannin). The quantification results demonstrated that QI aqueous extract contained significantly higher gallotannin (75.0 μg/mL) compared to QI methanol extract (46.8 μg/mL). Furthermore, the aqueous extract also exhibited significant higher antioxidant activity compared to the methanol extract at concentration of 2 μg/mL. &lt;strong&gt;Conclusions:&lt;/strong&gt; This study strongly support the utilization of water solvent for optimum gallotannin extraction from QI galls.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1195</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nur Alisa Kamarudin&lt;sup&gt;1&lt;/sup&gt;, Norhazilah Muhamad&lt;sup&gt;1,2&lt;/sup&gt;, Nik Nur Hakimah Nik Salleh&lt;sup&gt;1&lt;/sup&gt;, Suat Cheng Tan&lt;sup&gt;1,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;School of Health Sciences, Health Campus, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Medicine, Medical Campus, University Sultan Zainal Abidin, 20400 Kuala Terengganu, Terengganu, MALAYSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">V Sebastin</style></author><author><style face="normal" font="default" size="100%">G Gopalakrishnan</style></author><author><style face="normal" font="default" size="100%">M Sreejith</style></author><author><style face="normal" font="default" size="100%">KI Anoob Kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In vitro and In vivo Antidiabetic Evaluation of Whole Plant Extracts of Argyreia imbricata (Roth) Sant. and Patel</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Argyreia imbricata extracts</style></keyword><keyword><style  face="normal" font="default" size="100%">in vitro antidiabetic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">In vivo antidiabetic activity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">30-36</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Plants of the genus Argyreia have been used in traditional and folk medicines and a variety of pharmacological activities have also been reported. &lt;strong&gt;Objective: &lt;/strong&gt;The present study was aimed to evaluate the antidiabetic activity&lt;em&gt; in vitro &lt;/em&gt;and in&lt;em&gt; vivo &lt;/em&gt;of the different extracts of the whole plant &lt;em&gt;Argyreia imbricata. &lt;/em&gt;&lt;strong&gt;Materials and Methods: &lt;/strong&gt;The powdered material of the whole plant &lt;em&gt;Argyreia imbricata&lt;/em&gt; was extracted with solvents such as petroleum ether, chloroform, ethyl acetate and methanol by soxhelation. &lt;em&gt;In vitro&lt;/em&gt; antidiabetic activity of all the extracts was evaluated by α–amylase and α–glucosidase inhibition assay. Based on the results of &lt;em&gt;in vitro &lt;/em&gt;evaluation, the extracts selected were subjected to &lt;em&gt;in vivo &lt;/em&gt;evaluation on the Wistar albino rats with streptozotocin-induced diabetes mellitus. Initially, acute toxicity of the extracts was evaluated and the effective dose (ED&lt;sub&gt;50&lt;/sub&gt;) was fixed. Standard drug Glibenclamide was used for the comparative evaluation. Two doses of test extracts, low dose and high dose were administered to the test animals and their antidiabetic activity was evaluated by means of monitoring the changes in the blood glucose level, hematological and biochemical parameters and histopathology of liver and pancreas of test animals. &lt;strong&gt;Results: &lt;/strong&gt;Based on the results of &lt;em&gt;in vitro &lt;/em&gt;evaluation, the ethyl acetate and methanol extracts were selected for the in vivo evaluation. ED50 of the test extracts were fixed as 200mg.kg&lt;sup&gt;-1&lt;/sup&gt;. Two doses, 200mg.kg&lt;sup&gt;-1&lt;/sup&gt; and 400mg.kg&lt;sup&gt;-1&lt;/sup&gt; of the test extracts were subjected to evaluation. Both the tested extracts possessed the activity, but the methanol, extracts showed significant activity in all aspects. &lt;strong&gt;Conclusion: &lt;/strong&gt;Results of the present study strongly support the antidiabetic activity of tested extracts. Further studies on toxicity, identification isolation of the potential compounds may give useful results for the development of clinically useful chemotherapeutic agents in the future.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">30</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;V. Sebastin&lt;sup&gt;1,&lt;/sup&gt;*, G. Gopalakrishnan&lt;sup&gt;2&lt;/sup&gt;, M. Sreejith&lt;sup&gt;3&lt;/sup&gt;, K. I. Anoob Kumar&lt;sup&gt;4&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Associate Professor, Department of Pharmaceutical Chemistry, Malik Deenar College of Pharmacy, Seethangoli, Kasaragod, Kerala, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Assistant Professor, Department of Pharmacy, Annamalai University, Annamalai Nagar, Chidambaram, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Professor, Department of Pharmaceutical Chemistry, Nazareth College of Pharmacy, Thiruvalla, Pathanamthitta, Kerala, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Associate Professor, Department of Pharmaceutical Chemistry, KVM College of Pharmacy, Cherthala, Alappuzha, Kerala, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">K. I. Anoob Kumar</style></author><author><style face="normal" font="default" size="100%">M. Swamivel Manickam</style></author><author><style face="normal" font="default" size="100%">M. Sreejith</style></author><author><style face="normal" font="default" size="100%">V. Sebastin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Vitro and In Vivo Anti-Inflammatory Evaluation of the Whole Plant Extracts of Crotalaria Biflora (L)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Crotalaria biflora extracts</style></keyword><keyword><style  face="normal" font="default" size="100%">In vitro anti-inflammatory evaluation</style></keyword><keyword><style  face="normal" font="default" size="100%">In vivo antiinflammatory evaluation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">620-625</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Several species of Crotalaria are cultivated and consumed across the world by the rural population for a variety of purposes that include medicine, food, green manure, fodder etc. Objective: The present study was aimed to evaluate the anti-inflammatory activity of different extracts of the whole plant&lt;em&gt; Crotalaria biflora&lt;/em&gt; by&lt;em&gt; in vitro &lt;/em&gt;and &lt;em&gt;in vivo&lt;/em&gt; methods. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The powdered material of the whole plant &lt;em&gt;Crotalaria biflora &lt;/em&gt;was extracted by soxhelation with different solvents such as petroleum ether, chloroform, ethyl acetate and methanol. Stabilization of human red blood cell (HRBC) membrane is the method employed for the &lt;em&gt;in vitro&lt;/em&gt; evaluation. The extracts selected based on the results of &lt;em&gt;in vitro &lt;/em&gt;evaluation was further subjected to&lt;em&gt; in vivo &lt;/em&gt;evaluation by carrageenan-induced rat paw oedema method. In both &lt;em&gt;in vitro &lt;/em&gt;and &lt;em&gt;in vivo&lt;/em&gt; evaluations, Indomethacin was used as the standard control. Results: Among the four tested extracts in six different concentrations subjected to the &lt;em&gt;in vitro &lt;/em&gt;evaluation, the ethyl acetate and methanol extracts (1000μg/ml) showed significant activity which was selected for the &lt;em&gt;in vivo&lt;/em&gt; evaluation. Among the two doses of extracts (200mg.kg&lt;sup&gt;-1&lt;/sup&gt; and 400mg.kg&lt;sup&gt;-1&lt;/sup&gt;) selected for the &lt;em&gt;in vivo&lt;/em&gt; evaluation, the methanol extract (400mg.kg-1) showed significant activity followed by the ethyl acetate extract in the same dose. &lt;strong&gt;Conclusion: &lt;/strong&gt;Further studies on the phytochemicals present in these extracts may give more significant results&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">620</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;K. I. Anoob Kumar&lt;sup&gt;1,&lt;/sup&gt;*, M. Swamivel Manickam&lt;sup&gt;2&lt;/sup&gt;, M. Sreejith&lt;sup&gt;3&lt;/sup&gt;, V. Sebastin&lt;sup&gt;4&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Chemistry, KVM College of Pharmacy, Cherthala, Alappuzha, Kerala, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacy, Annamalai University, Annamalai Nagar, Chidambaram, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmaceutical Chemistry, Nazareth College of Pharmacy, Thiruvalla, Pathanamthitta, Kerala, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmaceutical Chemistry, Malik Deenar College of Pharmacy, Seethangoli, Kasaragod, Kerala, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Numlil Khaira Rusdi</style></author><author><style face="normal" font="default" size="100%">Erni Hernawati Purwaningsih</style></author><author><style face="normal" font="default" size="100%">Andon Hestiantoro</style></author><author><style face="normal" font="default" size="100%">Berna Elya</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In Vivo Antimammary Tumor Effects of Soybean Extract with Targeted Lunasin (ET-Lun)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Breast cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">EGFR</style></keyword><keyword><style  face="normal" font="default" size="100%">HER2</style></keyword><keyword><style  face="normal" font="default" size="100%">In-vivo</style></keyword><keyword><style  face="normal" font="default" size="100%">Soybean</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1269-1276</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background/Objective: &lt;/strong&gt;Lunasin is a peptide, consist of 44 amino acids which have anti-cancer, antioxidant, and anti-inflammatory activity. The price of commercial Lunasin was very expensive due to the high cost of lunasin synthesis and the lack of methods to obtain the pure lunasin weight from plant sources, involving time-consuming analytical instruments. To overcome these problems, the soybean extract with targeted Lunasin (ET-Lun) was made. The aim of this study was to investigate anti-cancer properties of ET-Lun in breast cancer models &lt;em&gt;in vivo&lt;/em&gt;. &lt;strong&gt;Methods:&lt;/strong&gt; Effect of ET-Lun was evaluated in 7,12-Dimetilbenz[a]antrasen (DMBA) induced breast cancer rat model. Tumor Mass, volume, and number were measured. The expression of HER2 and EGFR from each treatment group in DMBA-induced rat was evaluated using immunohistochemistry. &lt;strong&gt;Results: &lt;/strong&gt;The results shown that ET-Lun could reduced tumor volume (p=0,021). ET-Lun decreased EGFR expression compared to negative control DMBA (p=0,012). &lt;strong&gt;Conclusions: &lt;/strong&gt;These results indicated that the ET-Lun has anti-breast cancer activit&lt;em&gt;y in vivo.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1269</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Numlil Khaira Rusdi&lt;sup&gt;1,2&lt;/sup&gt;, Erni Hernawati Purwaningsih&lt;sup&gt;3,7&lt;/sup&gt;, Andon Hestiantoro&lt;sup&gt;4&lt;/sup&gt;, Berna Elya&lt;sup&gt;5&lt;/sup&gt;, Kusmardi Kusmardi&lt;sup&gt;6-8,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctoral Program for Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Pharmacy and Sciences, Universitas Muhammadiyah Prof. DR. Hamka, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacy, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department Obstetrics and Gynaecology, School of Medicine, Universitas Indonesia, Dr Cipto Mangunkusumo Hospital, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Phytochemistry, Faculty of Pharmacy, Universitas Indonesia, Depok, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Anatomic Pathology, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA. '&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Drug Development Research Cluster, Indonesian Medical Education and Reseach Institute, Universitas INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;8&lt;/sup&gt;Human Cancer Research Cluster, Indonesian Medical Education and Research Institute, Universitas INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Saleh A Almatroodi</style></author><author><style face="normal" font="default" size="100%">Mohammed A Alsahli</style></author><author><style face="normal" font="default" size="100%">Ahmad Almatroudi</style></author><author><style face="normal" font="default" size="100%">Amjad Ali Khan</style></author><author><style face="normal" font="default" size="100%">Arshad Husain Rahmani</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Peppermint, (Mentha × piperita): Role in Management of Diseases through Modulating Various Biological Activities</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-microbial</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Mentha ×piperita</style></keyword><keyword><style  face="normal" font="default" size="100%">Pathogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Peppermint</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">822-827</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Peppermint, (&lt;em&gt;Mentha&lt;/em&gt; ×piperita), aromatic perennial herb of the mint family (Lamiaceae). It is a natural hybrid of &lt;em&gt;Mentha spicata&lt;/em&gt; and&lt;em&gt; Mentha aquatica&lt;/em&gt; and is found wild with its parent species in central as well as southern Europe. It holds various types of ingredients including menthol, menthone and cineol. Menthol, which is extracted from peppermint, play an important role in the inhibition of various types of pathogenesis. Peppermint oil also acts as a mild carminative agent and used for disorder of the large intestines that causes stomach pain. Moreover, experimental studies have confirmed its role in health management through anti-oxidant, antiinflammatory, anti-inflammatory, anti-diabetic, neuroprotection and hepatoprotective effects. its topical application shows relief from cold, muscle pain, and headache. The health promoting role of Peppermint has gained a noteworthy scientific attention, but the exact mechanism of its action still remains not clear. The current review mainly emphases on the pharmalogical effects of peppermint in the inhibition of pathogenesis. The purpose of this review is to provide an overview of peppermint in the management of various types of diseases.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">822</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Saleh A. Almatroodi&lt;sup&gt;1&lt;/sup&gt;, Mohammed A. Alsahli&lt;sup&gt;1&lt;/sup&gt;, Ahmad Almatroudi&lt;sup&gt;1&lt;/sup&gt;, Amjad Ali Khan&lt;sup&gt;2&lt;/sup&gt;, Arshad Husain Rahmani&lt;sup&gt;1,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Medical Laboratories, College of Applied Medical Science, Buraidah 52571, Qassim University, SAUDI ARABIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Basic Health Sciences, College of Applied Medical Sciences, Qassim University, Buraydah, SAUDI ARABIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">SM Abdul Aziz Barbhuiya</style></author><author><style face="normal" font="default" size="100%">SH Victoria Devi</style></author><author><style face="normal" font="default" size="100%">Ajay Kakati</style></author><author><style face="normal" font="default" size="100%">Rejwan Ahmed Choudhury</style></author><author><style face="normal" font="default" size="100%">Muslek Uddin Mazumder</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharamacognostic Profile and Comparative in vitro Anti- Inflammatory Activity Study of Ethanomedicinal Plants of North East India</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory</style></keyword><keyword><style  face="normal" font="default" size="100%">Diclofenac sodium</style></keyword><keyword><style  face="normal" font="default" size="100%">Macroscopic</style></keyword><keyword><style  face="normal" font="default" size="100%">Microscopic</style></keyword><keyword><style  face="normal" font="default" size="100%">Northeast India</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognostic study</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">317-324</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; In ethno-medicinal practices, the leaves of &lt;em&gt;Alocasia macrrorhizos&lt;/em&gt;, &lt;em&gt;Canavalia ensiformis, Amaranthus cruentus, Averrhoea carambola, Bauhina tenifloara&lt;/em&gt;&amp;nbsp;and &lt;em&gt;Capsicum Chinese&lt;/em&gt; have different pharmacological activities. The problem encountered with the proper utilization of herbal drugs is lack of documentation and standard parameter, which create problem in acceptance and importance of these plants. &lt;strong&gt;Objective:&lt;/strong&gt; The objectives of our study are to establish scientifically evaluated pharmacognostic profile and &lt;em&gt;in vitro&lt;/em&gt; antiinflammatory screening of six plants. &lt;strong&gt;Methods:&lt;/strong&gt; Leaf sample from each plant was evaluated by macroscopic, microscopic and physicochemical parameters (As per WHO recommended methods of standardization). The anti-inflammatory activity screening of methanolic extracts was carried out against inhibition of protein denaturation method taking diclofenac sodium as a benchmark. &lt;strong&gt;Results: &lt;/strong&gt;The macroscopic characteristic and microscopical evaluation reveals the type of stomata within the leaves and presence of parenchyma cells, collenchyma cells, upper epidemis, lower epidermis, vascular bundle, palisade cells and trichomes in the transverse section of leaves. Physicochemical parameter reveals the total ash, acid insoluble ash, water soluble, methanol soluble extractives and moisture content. The IC&lt;sub&gt;50&lt;/sub&gt; value of &lt;em&gt;MEAM, MECE, MEAC, MEAC1, MECC&lt;/em&gt;&amp;nbsp;and &lt;em&gt;MEBT&lt;/em&gt; against inhibiton of protein denaturation was found to be 72.88, 841.78, 735.12, 303.75, 188, and 354.1855 μg/mL respectively. &lt;strong&gt;Conclusion: &lt;/strong&gt;The present study contributes useful information that will help in the exact identification as well as assessment of purity of crude drugs. Methanolic extract of&lt;em&gt; Alocasia macrorrhizos&lt;/em&gt; could be a potential anti-inflammatory agent from the natural sources.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">317</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;SM Abdul Aziz Barbhuiya, SH Victoria Devi*, Ajay Kakati, Rejwan Ahmed Choudhury, Muslek Uddin Mazumder&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Regional Institute of Paramedical and Nursing Sciences, Zemabawk, Aizwal - 796017, Mizoram, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Darunee Puangpronpitag</style></author><author><style face="normal" font="default" size="100%">Puangpaka Tankitjanon</style></author><author><style face="normal" font="default" size="100%">Adisak Sumalee</style></author><author><style face="normal" font="default" size="100%">Ampa Konsue</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Screening and Antioxidant Activities of the Seedling Extracts from Inca Peanut Plukenetia volubilis</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Inca peanut seedling</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolic compounds</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical screening</style></keyword><keyword><style  face="normal" font="default" size="100%">Plukenetia Volubilis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">52-58</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Plukenetia volubilis&lt;/em&gt; L., Inca peanut is an oleaginous plant, widely cultivated as commercially in South East Asia, especially in Thailand. The oil from the seed plant is a greatest interesting a natural source. &lt;strong&gt;Objectives:&lt;/strong&gt; The aims of this study were investigated phytochemical screening, to evaluated the total flavonoids and phenolic compound contents as well as antioxidant activities of seedling extract from &lt;em&gt;P. volubilis. &lt;/em&gt;&lt;strong&gt;Methods: &lt;/strong&gt;The dried &lt;em&gt;P. volubilis&lt;/em&gt; seedlings of 21 days growing period were extracted by using different solvent including aqueous (ASS), 50% ethanolic (HESS), and 95% ethanolic (ESS) extracts. The phytochemical screenings were determined on total phenolic compound (TPC) and flavonoid (TFC) contents. The antioxidation were tested by using 2,2-diphenyl-1-picrylhydrazy radical scavenging (DPPH), 2,2 -azinobis-(3-ethylbenzothiazoline-6-sulphonate) (ABTS&lt;sup&gt;+&lt;/sup&gt;) assay, and ferric reducing antioxidant power (FRAP). &lt;strong&gt;Results: &lt;/strong&gt;The results found that the ESS were significantly highest amount on total phenolic compound (23.0809±0.8632 mgGE/gExt ) and flavonoid (466.3839±1.5580 mgQE/gExt) contents. In this study, ascorbic acid (IC&lt;sub&gt;50 &lt;/sub&gt;=0.016±0.0003 mg/mL) and Trolox (IC&lt;sub&gt;50&lt;/sub&gt; =0.044±0.0008 mg/mL) as standard substances were showed more potent than all of the extracts from &lt;em&gt;P. volubilis &lt;/em&gt;seedlings. Surprisingly, the ESS has more potent on free radical scavenging higher than different solvents; DPPH=0.007± 0.001 (IC&lt;sub&gt;50&lt;/sub&gt;=mg/mL), ABTS= 1.4065± 0.0505 (IC&lt;sub&gt;50&lt;/sub&gt;=mg/mL),and FRAP= 74.4960± 2.6067 (mg=TE/gExt). &lt;strong&gt;Conclusion:&lt;/strong&gt; the plant seedling extracts composed with high amount of flavonoids and phenolic compound contents possess valuable to antioxidant activities. The seedling extracts from the plant could apply to supplementary food, cosmetic, pharmaceutical, and horticultural industries. Next study, chemical compositions, the major active compound(s), and biological activities will be clarified.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">52</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Darunee Puangpronpitag&lt;sup&gt;1&lt;/sup&gt;, Puangpaka Tankitjanon&lt;sup&gt;2&lt;/sup&gt;, Adisak Sumalee&lt;sup&gt;2&lt;/sup&gt;, Ampa Konsue&lt;sup&gt;3,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Biomedical Research Unit, Faculty of Medicine, Mahasarakham University, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Sukhothai Thammatirat Open University, Nonthaburi, 11120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Thai Traditional Medicinal Research Unit, Applied Thai Traditional Medical Program, Faculty of Medicine, Mahasarakham University, Maha Sarakham, 44000, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mruthunjaya Kenganora</style></author><author><style face="normal" font="default" size="100%">Sushma Rudraswamy</style></author><author><style face="normal" font="default" size="100%">Jai Shankar Puttabuddi Hombarvalli</style></author><author><style face="normal" font="default" size="100%">Nagabhushana Doggalli</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemicals  A Novel Therapeutic Approach to Control Oral Biofilm</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Dental plaque</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal herbs</style></keyword><keyword><style  face="normal" font="default" size="100%">Microbial resistance</style></keyword><keyword><style  face="normal" font="default" size="100%">Oral biofilm</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant extracts</style></keyword><keyword><style  face="normal" font="default" size="100%">Quorum sensing</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">730-736</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Humans and micro-organisms have co-evolved having a synergetic relationship with their resident microbiome. The mouth features a diverse microbiota that grows on oral surfaces as functionally and structurally organized biofilms. The oral biofilms are accountable for causing a wide range of chronic diseases and owing to the development of antibiotic-resistant bacteria it has really become tough to treat with efficacy. Operative control of oral biofilm and the resulting infectious diseases epitomizes a significant universal challenge. For this kind of therapeutics, natural herbal products are perfect candidates because of their unique properties. The current review presents a novel approach to control and eradicate oral biofilm by the phytochemicals. Research on phytochemicals is zealously focused on health promotion, disease prevention, and also on the development of novel therapeutic interventions.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">730</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Mruthunjaya Kenganora&lt;sup&gt;1&lt;/sup&gt;, Sushma Rudraswamy&lt;sup&gt;2,&lt;/sup&gt;*, Jai Shankar Puttabuddi Hombarvalli&lt;sup&gt;3&lt;/sup&gt;, Nagabhushana Doggalli&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, J.S.S College of Pharmacy, Mysore, J.S.S Academy of Higher Education and Research, Mysore, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Public Health Dentistry, J.S.S Dental College and Hospital, J.S.S Academy of Higher Education and Research, Mysore, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Oral Medicine and Radiology, J.S.S Dental College and Hospital, J.S.S Academy of Higher Education and Research, Mysore, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Oral Medicine and Radiology, J.S.S Dental College and Hospital, J.S.S Academy of Higher Education and Research, Mysore, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Elvan Wiyarta</style></author><author><style face="normal" font="default" size="100%">Ari Estuningtyas</style></author><author><style face="normal" font="default" size="100%">Nurhuda Sahar</style></author><author><style face="normal" font="default" size="100%">Yurnadi Hanafi Midoen</style></author><author><style face="normal" font="default" size="100%">Aryo Tedjo</style></author><author><style face="normal" font="default" size="100%">Alfred Pakpahan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Potential Inhibition by Phaleria macrocarpa Leaves Ethanol Extract on Ki-67 Expression in Distal Colon Mouse</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Dextran sodium sulphate</style></keyword><keyword><style  face="normal" font="default" size="100%">Inflamation</style></keyword><keyword><style  face="normal" font="default" size="100%">Ki- 67</style></keyword><keyword><style  face="normal" font="default" size="100%">Mahkota Dewa (Phaleria macrocarpa)</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">443-449</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Ulcerative colitis (UC) has been an important aspect of an incurable chronic inflammatory disease over the last few decades. To find useful therapies for UC, one of which is herbal therapy, many researches have been conducted. Due to its anti-inflammatory effects, &lt;em&gt;Phaleria macrocarpa &lt;/em&gt;(PM), an Indonesian indigenous herb, is considered to be the alternative therapy for UC.&lt;em&gt; Phaleria macrocarpa &lt;/em&gt;Leaves Ethanol Extract (PMLEE) is then used in this research to determine its effect on UC by using Ki-67 as a marker of proliferation. PMLEE was created from dry PM content undergoing maceration. The animals were classified into six categories: normal, positive control, negative control and PMLEE group (100, 200, 300 mg/kgBW). PMLEE was then injected for 7 consecutive days into BALB/c mice that were caused by dextran sodium sulphate (DSS). DSS is used for modeling UC in the colon tissue of mice. All mice were terminated and then stained with anti-Ki-67 after their colons were extracted. Subsequently, the stained parts were analyzed with ImageJ based on the color intensity produced by the results of H-score. Based on H-score, PMLEE 300mg and 200mg has significantly decreased the expression of Ki-67 compare to the negative control (p=0.001 and p=0.01). PMLEE also has a tendency to be dose dependent based on the significant difference from PMLEE 300mg and 100mg (p=0.002). It then concludes that PMLEE is related to Ki-67 expression in cells, as it was inversely proportional in this analysis.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">443</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kusmardi Kusmardi&lt;sup&gt;1,&lt;/sup&gt;*, Elvan Wiyarta&lt;sup&gt;2&lt;/sup&gt;, Ari Estuningtyas&lt;sup&gt;3&lt;/sup&gt;, Nurhuda Sahar&lt;sup&gt;4&lt;/sup&gt;, Yurnadi Hanafi Midoen&lt;sup&gt;4&lt;/sup&gt;, Aryo Tedjo&lt;sup&gt;5&lt;/sup&gt;, Alfred Pakpahan&lt;sup&gt;6&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anatomic Pathology, Drug Development Research Cluster, Human Cancer Research Center, IMERI, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya 6 Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya 6 Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacology and Therapeutic, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya 6 Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya 6 Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Medical Chemistry, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Jakarta, INDONESIA. 6Department of Oral Biology, Faculty of Dentistry, Universitas Trisakti, Jl. Kyai Tapa Jakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Elvan Wiyarta</style></author><author><style face="normal" font="default" size="100%">Ari Estuningtyas</style></author><author><style face="normal" font="default" size="100%">Nurhuda Sahar</style></author><author><style face="normal" font="default" size="100%">Yurnadi Hanafi Midoen</style></author><author><style face="normal" font="default" size="100%">Aryo Tedjo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Potential of Phaleria macrocarpa Leaves Ethanol Extract to Upregulate the Expression of Caspase-3 in Mouse Distal Colon after Dextran Sodium Sulphate Induction</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Apoptosis</style></keyword><keyword><style  face="normal" font="default" size="100%">Inflammation</style></keyword><keyword><style  face="normal" font="default" size="100%">Mahkota Dewa</style></keyword><keyword><style  face="normal" font="default" size="100%">Ulcerative colitis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">23-29</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Ulcerative colitis (UC) is a part of incurable chronic inflammatory disease that has gained importance over the past few decades. A lot of research has been done to find effective treatments for UC, one of which is herbal medicine. &lt;em&gt;Phaleria macrocarpa&lt;/em&gt; (PM), an Indonesian native plant, is thought to be an alternative therapy for UC because of its anti-inflammatory properties. Therefore, in this research, &lt;em&gt;Phaleria macrocarpa&lt;/em&gt; Leaves Ethanol Extract (&lt;em&gt;PM&lt;/em&gt;LEE) is used to assess its effect on UC by using Caspase-3 as apoptosis marker. PMLEE was made from dried material of PM that undergo maceration. Animals were separated into six groups: normal, negative control, positive control, and PMLEE groups (100, 200, 300 mg/kgBW). PMLEE was then injected to BALB/c mice that have been induced by dextran sodium sulphate (DSS) for 7 consecutive days. DSS is used to model UC in mice colon tissue. All animals were sacrificed and their colons were collected then stained with anti-Caspase-3. The stained sections were subsequently examined with ImageJ based on color intensity which generated H-Score as the results. Based on H-Score of each group, PMLEE 300mg has significantly upregulate the expression of Caspase-3 compare to the negative control (p=0.015). PMLEE also has a tendency to be dose dependent based on the significant difference between PMLEE doses. Therefore, it concludes that PMLEE is able to upregulate the expression of Caspase-3 in colon cells as in this study it was directly proportional. &lt;strong&gt;Key words:&lt;/strong&gt; Mahkota Dewa, Inflammation, Apoptosis, Ulcerative colitis.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">23</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kusmardi Kusmardi&lt;sup&gt;1&lt;/sup&gt;, Elvan Wiyarta&lt;sup&gt;2,&lt;/sup&gt;*, Ari Estuningtyas&lt;sup&gt;3&lt;/sup&gt;, Nurhuda Sahar&lt;sup&gt;4&lt;/sup&gt;, Yurnadi Hanafi Midoen&lt;sup&gt;4&lt;/sup&gt;, Aryo Tedjo&lt;sup&gt;5 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anatomic Pathology, Drug Development Research Cluster, Human Cancer Research Center, IMERI, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya 6 Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya 6 Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacology and Therapeutic, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya 6 Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya 6 Jakarta, INDONESIA&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;5Department Medical Chemistry, Faculty of Medicine, Universitas Indonesia, Jl. Salemba Raya 6 Jakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shalini K</style></author><author><style face="normal" font="default" size="100%">Ilango K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Preliminary Phytochemical Studies, GC-MS Analysis and In vitro Antioxidant Activity of Selected Medicinal Plants and its Polyherbal Formulation</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Macroscopical</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical</style></keyword><keyword><style  face="normal" font="default" size="100%">Polyherbal formulation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">648-659</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Novel polyherbal formulation (PHF) is the utilization of more than one herb in the preparation of herbal medication. The thought is found in the conventional system of medicine where the variety of herbs in a specific proportion of illness. Because of synergism, polyherbalism presents a few advantages which aren’t accessible in single herbal medication. It is utilized in these medications for the treatment of numerous sicknesses including antioxidants. &lt;strong&gt;Objective: &lt;/strong&gt;To develop a phytochemical screening and GC-MS analysis of Novel Polyherbal formulation for &lt;em&gt;In vitro&lt;/em&gt; antioxidant activity. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Macroscopical, preliminary phytochemical, quantitative phytoconstituents, and In-vitro antioxidant activity of all the individual extract and polyherbal formulation was done by chemical method. Identification of phytoconstituents with the aid of Gas chromatography – Mass spectroscopy (GC-MS).&lt;strong&gt; Results:&lt;/strong&gt; Macroscopical study and physicochemical examination, for example, ash value, extractive value, loss on drying, and pH were reported to&lt;em&gt; A. racemosus, B. variegata, C. bonducella, S. asoka,&lt;/em&gt; and &lt;em&gt;S. racemosus&lt;/em&gt; and novel polyherbal formulation. Qualitative phytochemical investigation revealed the presence of alkaloids, flavonoids, gums &amp;amp; mucilage, carbohydrates, steroids, proteins &amp;amp; amino acids, fats &amp;amp; fixed oils, glycoside, phenols, and saponins. Quantitative estimation such as TAC, TFC, TGC, TSC, and TPC was showed positive results. All the individual extract and PHF were subjected to GC-MS analysis. All the individual extract and polyherbal formulation displayed strong antioxidant activity. &lt;strong&gt;Conclusions:&lt;/strong&gt; To conclude the PHF was reported that high level of bioactive contents present and strong antioxidant activity in contrast to the preferred ascorbic acid. The GC-MS uncovered the presence of bioactive compounds and these compounds are suggested to treat antibacterial, antioxidant, anti-inflammatory, and antiviral, anti-tumor, anti-proliferative activity, and antifungal activity.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">648</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Shalini K&lt;sup&gt;1&lt;/sup&gt;, Ilango K&lt;sup&gt;2,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Pharmacognosy and Phytochemistry, Interdisciplinary Institute of Indian System of Medicine (IIISM), SRM Institute of Science and Technology, Kattankulathur - 603 203, Chengalpattu (Dt), Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Chemistry, SRM College of Pharmacy, SRM Institute of Science and Technology Kattankulathur-603 203, Chengalpattu (Dt), Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Namira Khairunnisa</style></author><author><style face="normal" font="default" size="100%">Feda Anisah Makkiyah</style></author><author><style face="normal" font="default" size="100%">Tashya Anggraeni Sinaga</style></author><author><style face="normal" font="default" size="100%">Rahmah Hida Nurrizka</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Prognostic Factors in Predicting Primary Brainstem Hemorrhage Patients: An Experience in Indonesia’s Rural Hospital</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Brainstem</style></keyword><keyword><style  face="normal" font="default" size="100%">Factor</style></keyword><keyword><style  face="normal" font="default" size="100%">Intracerebral hemorrhage</style></keyword><keyword><style  face="normal" font="default" size="100%">Primary</style></keyword><keyword><style  face="normal" font="default" size="100%">Prognosis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1445-1449</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Primary brainstem hemorrhage is a rare type of hemorrhagic stroke with a very high reported mortality rate in Indonesia.&lt;strong&gt; Aim:&lt;/strong&gt; This study aims to demonstrate the mortality rate of cases in one of Indonesia’s rural hospitals. To help reduce the mortality rate, the prognostic factors of several cases were studied. These steps are needed to be able to predict the prognosis of primary brainstem hemorrhage patients and to give a better explanation to the family of the patients. &lt;strong&gt;Methods:&lt;/strong&gt; A cross-sectional study was undertaken with collecting medical and radiological records from January 2018 to August 2020. A total sampling technique was done, and 340 patients were diagnosed with hemorrhagic stroke during that period. Only ten patients met the inclusion criteria and were included as the study samples. Statistical analysis using SPSS 22 and the Spearman correlation test adjusted for each variable. &lt;strong&gt;Results&lt;/strong&gt;: Low prevalence of primary brainstem hemorrhage (7%). There were correlation between GCS score, brainstem hemorrhage location, and length of stay with the patient’s prognosis.&lt;strong&gt; Conclusion:&lt;/strong&gt; Understanding these prognostic factors would reduce the prevalence of this primary brainstem hemorrhage and to ease the process of explaining the patients’ condition to the family.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1445</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Namira Khairunnisa&lt;sup&gt;1&lt;/sup&gt;, Feda Anisah Makkiyah&lt;sup&gt;1,*&lt;/sup&gt;, Tashya Anggraeni Sinaga&lt;sup&gt;1&lt;/sup&gt;, Rahmah Hida Nurrizka&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Medicine, Universitas Pembangunan Nasional Veteran Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Public Health, UIN Syarif hidayatullah, Jakarta&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amel CHOUABIA</style></author><author><style face="normal" font="default" size="100%">Samir DJEMLI</style></author><author><style face="normal" font="default" size="100%">Cherif ABDENNOUR</style></author><author><style face="normal" font="default" size="100%">Leila MALLEM</style></author><author><style face="normal" font="default" size="100%">Labiba KAHALERRAS</style></author><author><style face="normal" font="default" size="100%">Fatma Zohra ARKOUB</style></author><author><style face="normal" font="default" size="100%">Narimene BOUABDALLAH</style></author><author><style face="normal" font="default" size="100%">Abdelkrim TAHRAOUI</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Protective effect of Salvia officinalis against cypermethrininduced reprotoxicity in male Wistar rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cypermethrin</style></keyword><keyword><style  face="normal" font="default" size="100%">Histology</style></keyword><keyword><style  face="normal" font="default" size="100%">Rats</style></keyword><keyword><style  face="normal" font="default" size="100%">Salvia officinalis</style></keyword><keyword><style  face="normal" font="default" size="100%">Spermatozoa</style></keyword><keyword><style  face="normal" font="default" size="100%">Toxicity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1413-1421</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Medicinal plants are a reservoir of biologically active compounds with therapeutic properties that, over time, have been used for the treatment of various diseases. This study aims to evaluate the protective effect of the aqueous extract of the leaves of&lt;em&gt; Salvia officinalis &lt;/em&gt;against cypermethrin-induced toxicity. &lt;strong&gt;Methods: &lt;/strong&gt;30 male rats weighing approximately 240 g were divided into equal six groups; the control group received tap water, the positive control received the aqueous extract of sage leaves (SLE) at a dose of (0.5g/kg bw), the groups treated with cypermethrin (Cyp1) at 8.33 mg/kg bw and (Cyp2) at 25 mg/kg bw, and the groups treated by cypermethrin combined with aqueous extract of sage SLE+Cyp1 (0.5g/kg bw+8.33 mg/kg bw) and SLE+Cyp2 (0.5g/kg bw+25 mg/kg bw) for four days/week. After 4 weeks of oral administration, epididymal seminal fluid was analyzed via the CASA system, in addition to the histological study testis and epididymis. &lt;strong&gt;Results: &lt;/strong&gt;The obtained results showed a decrease in the absolute weight of the reproductive organs, with a significant decrease in sperm concentration, motility and speed in the cypermethrin-treated group compared to the control. Histological study of the testes and epididymis indicates an alteration in the stages of spermatogenesis in groups Cyp1 and Cyp2 compared to the control. However, the above-mentioned parameters were maintained almost normal in the groups that received the aqueous extract of sage with both doses of cypermethrin. &lt;strong&gt;Conclusion:&lt;/strong&gt; it can be demonstrated that SLE has been shown to protect rats from cypermethrin-induced reprotoxicity.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1413</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Amel CHOUABIA&lt;sup&gt;1&lt;/sup&gt;, Samir DJEMLI&lt;sup&gt;2&lt;/sup&gt;,*, Cherif ABDENNOUR&lt;sup&gt;1&lt;/sup&gt;, Leila MALLEM&lt;sup&gt;1&lt;/sup&gt;, Labiba KAHALERRAS&lt;sup&gt;1&lt;/sup&gt;, Fatma Zohra ARKOUB&lt;sup&gt;1&lt;/sup&gt;, Narimene BOUABDALLAH&lt;sup&gt;1&lt;/sup&gt;, Abdelkrim TAHRAOUI&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Sciences, Animal Ecophysiology Laboratory, Department of Biology, Badji Mokhtar University, Annaba, ALGERIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Sciences, Applied Neuroendocrinology Laboratory, Department of Biology, Badji Mokhtar University, Annaba, ALGERIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Numlil Khaira Rusdi</style></author><author><style face="normal" font="default" size="100%">Weri Lia Yuliana</style></author><author><style face="normal" font="default" size="100%">Erni Hernawati Purwaningsih</style></author><author><style face="normal" font="default" size="100%">Andon Hestiantoro</style></author><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Subchronic Toxicity of Lunasin Targeted Extract (ET-Lun) from Soybean Seed (Glycine max (L.) Merr.): Perspective from Liver Histopathology, SGOT, and SGPT Levels in Sprague Dawley Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Liver</style></keyword><keyword><style  face="normal" font="default" size="100%">Lunasin</style></keyword><keyword><style  face="normal" font="default" size="100%">SGOT</style></keyword><keyword><style  face="normal" font="default" size="100%">SGPT</style></keyword><keyword><style  face="normal" font="default" size="100%">Soybean</style></keyword><keyword><style  face="normal" font="default" size="100%">Subchronic Toxicity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1384-1388</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Lunasin Targeted Extract (ET-Lun) has a pharmacology effect in inhibiting inflammation by decreasing COX-2 and iNOS expression. ET-Lun could increase apoptosis and decrease dysplasia (p &amp;gt; 0,05). In addition, ET-Lun could decrease EGFR expression in breast cancer rats. The acute toxicity showed ET-Lun has LD50 more than 5000 mg/kg BW and was practically non-toxic. Objective: this study aimed to determine the subchronic toxicity of ET-Lun. &lt;strong&gt;Methods: &lt;/strong&gt;Male and female Sprague Dawley rats (n=40) were divided into 4 groups, the control group and treatment group ET-Lun dose of 250 mg/Kg BW, 500 mg/kg BW, and 750 mg/kg BW. The ET-Lun was administered for 90 days. On the 91st day, the animals were dissected and examined for SGOT-SGPT levels, liver histopathology, and diameter of the central vein.&lt;strong&gt; Results:&lt;/strong&gt; The SGOT-SGPT levels showed no significant difference between the treatment group and the control group (p &amp;gt; 0.05). On microscopic observation, there was no change or damage to the liver of rats in each group. The diameter of the central vein of the rat liver shows no significant difference between the control and treatment groups. &lt;strong&gt;Conclusion:&lt;/strong&gt; The ET-Lun does not produce adverse effects in liver rats after subchronic treatment.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1384</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Numlil Khaira Rusdi&lt;sup&gt;1,2&lt;/sup&gt;, Weri Lia Yuliana&lt;sup&gt;2&lt;/sup&gt;, Erni Hernawati Purwaningsih&lt;sup&gt;3,4&lt;/sup&gt;, Andon Hestiantoro&lt;sup&gt;5&lt;/sup&gt;, Kusmardi Kusmardi&lt;sup&gt;1,4,6,7,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Doctoral Program for Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Pharmacy and Sciences, Universitas Muhammadiyah Prof. DR. Hamka, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacy, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Drug Development Research Cluster, Indonesian Medical Education and Reseach Institute, Universitas INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department Obstetrics and Gynaecology, School of Medicine, Universitas Indonesia, Dr Cipto Mangunkusumo Hospital, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Anatomic Pathology, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Human Cancer Research Cluster, Indonesian Medical Education and Reseach Institute, Universitas INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sujithra M</style></author><author><style face="normal" font="default" size="100%">Vimala KS</style></author><author><style face="normal" font="default" size="100%">Sabitha M</style></author><author><style face="normal" font="default" size="100%">Priya S</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">An Analytical and in-vivo Study to Evaluate the Effect of Triphala Kaṣāya Vāsita Godhūma (Triticum aestivum grains soaked in Triphala Kaṣāya) on its Glycemic Index compared to Raw Godhūma (Raw Triticum aestivum grains)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ayurveda</style></keyword><keyword><style  face="normal" font="default" size="100%">Diabetes</style></keyword><keyword><style  face="normal" font="default" size="100%">Gluten</style></keyword><keyword><style  face="normal" font="default" size="100%">Glycemic index</style></keyword><keyword><style  face="normal" font="default" size="100%">Godhūma</style></keyword><keyword><style  face="normal" font="default" size="100%">Prameha</style></keyword><keyword><style  face="normal" font="default" size="100%">Triphala kaṣāya</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">526-534</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Diabetes is generally referred to as a Metabolic Disorder or a Lifestyle Disorder, that is mainly characterized by the symptom of Hyperglycemia caused by the defective insulin secretion, congenital or acquired. Diabetes requires management of diet and lifestyle with or without medications to keep the blood sugar under control. Foods with medium Glycemic Index (GI) is best preferred for Diabetics, because high GI foods will rapidly increase the blood sugar level, and low GI will cause grave health issues. In practice, wheat is the highly recommended diet for diabetics as the GI is medium in comparison to rice that belongs to a high GI group. But wheat causes digestive problems, and flatulence in addition to the Gluten allergy that many people suffer from. However in Āyurveda, the Classical Text Aṣṭāṅga Hṛdaya (AH) mentions in Prameha Cikitsa Adhyāya (Chapter on Treatment of Diabetes) that Godhūma (grains of Wheat - Triticum aestivum L) has to be kept soaked in Triphala Kaṣāya (Decoction prepared with the fruits of Terminalia chebula, T. bellerica and Phyllanthus emblica) and then dried and powdered before being used as a diet for a diabetic. The grains of Godhūma were kept soaked in Triphala Kaṣāya and then dried and powdered. A comparative analytical study was done for the two samples- treated wheat grains (Triphala Kaṣāya Vāsita Godhūma) and untreated/raw wheat grains. An In vivo study was also done to assess the GI value of both the samples of wheat. The analytical and In vivo study results prove that while the GI is still maintained within medium range, the allergen gluten is completely eliminated, total fat and total protein have reduced while still maintaining the nutritive value, in the treated sample when compared to the raw sample. Based on the results obtained from the analytical and in-vivo study, it can be concluded that Triphala Kaṣāya Vāsita Godhūma becomes even more compatible and healthy for a diabetic, in gluten allergy and discomforts caused by wheat consumption, in comparison to the untreated wheat grains.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">526</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sujithra M&lt;sup&gt;1,&lt;/sup&gt;*, Vimala KS&lt;sup&gt;2&lt;/sup&gt;, Sabitha M&lt;sup&gt;3&lt;/sup&gt;, Priya S&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;PG Scholar, Department of Dravya Guna Vijnana (Ayurvedic Pharmacology), Amrita School of Ayurveda, Amritapuri; Amrita Vishwa Vidyapeetham, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Professor, Department of Dravya Guna Vijnana (Ayurvedic Pharmacology), Amrita School of Ayurveda, Amritapuri; Amrita Vishwa Vidyapeetham, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Principal, Amrita School of Pharmacy, Cochin; Amrita Vishwa Vidyapeetham, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;HOD &amp;amp; Professor, Department of Dravya Guna Vijnana (Ayurvedic Pharmacology), Amrita School of Ayurveda, Amritapuri; Amrita Vishwa Vidyapeetham, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Victoria Vladimirovna Fedotova</style></author><author><style face="normal" font="default" size="100%">Dmitry Alexeevich Konovalov</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anatomical Characteristics of Leaves and Flowers of Cornus sanguine subsp. australis (C.A.Mey.) Jav.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Collenchyma</style></keyword><keyword><style  face="normal" font="default" size="100%">Cornus sanguinea subsp. australis (C.A.Mey.) Jav.</style></keyword><keyword><style  face="normal" font="default" size="100%">Cross-section</style></keyword><keyword><style  face="normal" font="default" size="100%">Mesophyll</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomatal anomocytic type</style></keyword><keyword><style  face="normal" font="default" size="100%">Vascular bundle</style></keyword><keyword><style  face="normal" font="default" size="100%">Т-shaped trichomes</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">448-451</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Cornus sanguinea &lt;/em&gt;subsp. &lt;em&gt;australis &lt;/em&gt;(C.A.Mey.) Jav. is a widespread plant of the Caucasus (Russia). This is a small decorative tree with a large mass of raw material of leaves and flowers, which contain phenolic compounds. Currently, this plant is used in traditional medicine in some countries. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;&lt;em&gt;C. australis &lt;/em&gt;leaves, and flowers were collected during the flowering period on the Mount Mashuk in Pyatigorsk, Stavropol region, Russia in June 2019. The anatomical structure of &lt;em&gt;C. australis &lt;/em&gt;is considered in accordance with the requirements of the State Pharmacopoeia XIV.&lt;strong&gt; Results:&lt;/strong&gt; There are heavily sinuous walls of cells of the upper and lower epidermis in microscopy of the leaves of &lt;em&gt;C. australis,&lt;/em&gt; stomatal anomocytic type, Т-shaped trichomes, two types of mesophyll: palisade and spongy. In the vascular system of the leaf and petiole, there are two vascular bundles: small and larger. In the small vascular bundle, the xylem is located from the abaxial surface, the phloem – from the adaxial surface, in the big vascular bundle on the contrary. The lower epidermis of the petal and sepal is covered with T-shaped trichomes. &lt;strong&gt;Conclusion: &lt;/strong&gt;Obtained anatomical signs are necessary for identification, authenticity, standardization for the use of &lt;em&gt;C. australis&lt;/em&gt; as raw materials for pharmaceutical purposes.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">448</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Victoria Vladimirovna Fedotova&lt;sup&gt;1&lt;/sup&gt;, Dmitry Alexeevich Konovalov&lt;sup&gt;1,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;Department of Pharmacognosy, Botany and Technology of Phytopreparations, Pyatigorsk Medical and Pharmaceutical Institute, a Branch of Volgograd State Medical University Ministry of Health of Russian Federation, Pyatigorsk, 357532, Kalinina 11, RUSSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">P Praveen Kumar</style></author><author><style face="normal" font="default" size="100%">K Prabhu</style></author><author><style face="normal" font="default" size="100%">Mudiganti Ram Krishna Rao</style></author><author><style face="normal" font="default" size="100%">Mallika Jain</style></author><author><style face="normal" font="default" size="100%">K Kalaivani</style></author><author><style face="normal" font="default" size="100%">Shruthi Dinakar</style></author><author><style face="normal" font="default" size="100%">Sampad Shil</style></author><author><style face="normal" font="default" size="100%">N Vijayalakshmi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anti-arthritic Property of Sahacharadi Kashayam Against Freund's Complete</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-arthritic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Arthritis</style></keyword><keyword><style  face="normal" font="default" size="100%">Biomarkers</style></keyword><keyword><style  face="normal" font="default" size="100%">Sahacharadi Kashayam</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">459-464</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;The available modern molecular drugs for the therapy of Rheumatoid arthritis are beset with several side effects and alternative drugs are urgently needed. The present investigation was performed to evaluate the anti-arthritic activity of Sahacharadi Kashayam (SK), an Ayurvedic formulation, against Freund's complete adjuvant (CFA) - induced arthritis in rats. &lt;strong&gt;Methods: &lt;/strong&gt;In this experimental trial, SK was administered at doses of 0.5, 1.0 and 1.5 ml/kg body weight orally to adjuvant (CFA) induced arthritic rats. The anti-arthritic activity was evaluated by using paw volume, haematological parameters and arthritic biomarkers. The efficacy of the Kashayam was compared with the standard Leflunomide (10 mg/kg) drug. &lt;strong&gt;Results: &lt;/strong&gt;Significant reduction in paw volume and thickness by SK (0.5 ml dose) has been found and there was considerably improvement in haematological parameters and arthritic markers in CFA rats till 14 days. After 14&lt;sup&gt;th&lt;/sup&gt; day SK treatment with doses (1.0 and 1.5ml), however, reoccurrence of inflammation and pathological changes were observed in rats.&lt;strong&gt; Conclusion: &lt;/strong&gt;The study clearly indicated the anti-arthritic role of SK. Future studies, however, are warranted to provide a new approach in relation to the therapeutic dose and treatment period of SK which may eventually lead to the development of a new category of the anti-arthritic agent.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">459</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;P Praveen Kumar&lt;sup&gt;1&lt;/sup&gt;, K Prabhu&lt;sup&gt;2&lt;/sup&gt;, Mudiganti Ram Krishna Rao&lt;sup&gt;3,&lt;/sup&gt;*, Mallika Jain&lt;sup&gt;4&lt;/sup&gt;, K Kalaivani&lt;sup&gt;5&lt;/sup&gt;, Shruthi Dinakar&lt;sup&gt;6&lt;/sup&gt;, Sampad Shil&lt;sup&gt;7&lt;/sup&gt;, N. Vijayalakshmi&lt;sup&gt;7&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Research Scholar, Sree Balaji Medical College and Hospital, Bharath University, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Associate Professor, Department of Anatomy, Sree Balaji Medical College and Hospital, Bharath University, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Professor, Department of Industrial Biotechnology, Bharath Institute of Higher Education and Research, Chennai, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Scientist, Bright Care Research Private Ltd, Chennai, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Professor, Indira Priyadarshini Dental College, Chennai, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Ayurvedic Practitioner, Kottakkal Arya Vaidhya Sala, Chennai, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;Student, Department of Industrial Biotechnology, Bharath Institute of Higher Education and Research, Chennai, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Raceline Gounoue Kamkumo</style></author><author><style face="normal" font="default" size="100%">Abel Narcisse Messi Betene</style></author><author><style face="normal" font="default" size="100%">Patrick Valere Tsouh Fokou</style></author><author><style face="normal" font="default" size="100%">Jean Hubert Donfack</style></author><author><style face="normal" font="default" size="100%">Marius Jaurès Tsakem Nangap</style></author><author><style face="normal" font="default" size="100%">Albertine Ngako</style></author><author><style face="normal" font="default" size="100%">Roberto Fokou</style></author><author><style face="normal" font="default" size="100%">Mariscal Brice Tchatat Tali</style></author><author><style face="normal" font="default" size="100%">Florence Ngueguim Tsofack</style></author><author><style face="normal" font="default" size="100%">Théophile Dimo</style></author><author><style face="normal" font="default" size="100%">Fabrice Fekam Boyom</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antimalarial Effects of the Aqueous Extract of Entandrophragma angolense Bark on Plasmodium berghei Infection in Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antiplasmodial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">E. angolense</style></keyword><keyword><style  face="normal" font="default" size="100%">Malaria infection</style></keyword><keyword><style  face="normal" font="default" size="100%">Mice</style></keyword><keyword><style  face="normal" font="default" size="100%">P. berghei</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">687-698</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Research for new antimalarial drugs remains a permanent quest for the control of malaria. &lt;strong&gt;Objective:&lt;/strong&gt; The present study investigates the effects of the aqueous extract of &lt;em&gt;Entandrophragma angolense&lt;/em&gt; bark on&lt;em&gt; P. berghei-&lt;/em&gt;induced malaria in mice. &lt;strong&gt;Methods: &lt;/strong&gt;Eight weeks old mice, were intraperitoneally infested with 200 μl of blood, containing 1x10&lt;sup&gt;6&lt;/sup&gt; &lt;em&gt;P. berghei&lt;/em&gt;-infected-erythrocytes. Parasitaemia was determined using a 10% giemsa stained blood smear read under optical microscope (x100). The infected animals were randomized into 5 groups of 10 animals each and daily treated for 5 days with the plant extract at 125, 250 and 500 mg/kg. The normal control and malaria control received water while the chloroquine control was treated with 10 mg/kg of chloroquine. Body weight, parasitaemia and survival time were monitored daily during treatment and follow up periods. Five animals from each group were sacrificed under anaesthesia at the end of treatment (d8) and after the follow up period (d28). Venous blood was used for haematological and biochemical tests. Organs (liver, kidneys and spleen) were also collected for biochemical and histological analyses. &lt;strong&gt;Results: &lt;/strong&gt;Administration of the aqueous extract of &lt;em&gt;E. angolense &lt;/em&gt;bark to infected mice significantly inhibited parasite development (&lt;em&gt;p&lt;/em&gt; &amp;lt;0.001) with ED&lt;sub&gt;50&lt;/sub&gt; estimated at 25.32 mg/kg. The extract prevented animal from death, body weight loss, anaemia, leucocytosis, high transaminases (ALT and AST), high bilirubin, creatinine and MDA levels, oxidative stress and anatomical alteration in organs as compared to the malaria control.&lt;strong&gt; Conclusion:&lt;/strong&gt; The &lt;em&gt;E. angolense &lt;/em&gt;bark possesses antimalarial properties, supporting its use in traditional medicine to treat malaria.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">687</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Raceline Gounoue Kamkumo&lt;sup&gt;1,2,&lt;/sup&gt;*, Abel Narcisse Messi Betene&lt;sup&gt;1,2&lt;/sup&gt;, Patrick Valère Tsouh Fokou&lt;sup&gt;2,3&lt;/sup&gt;, Jean Hubert Donfack&lt;sup&gt;4&lt;/sup&gt;, Marius Jaurès Tsakem Nangap&lt;sup&gt;1,2&lt;/sup&gt;, Albertine Ngako&lt;sup&gt;1,2&lt;/sup&gt;, Roberto Fokou&lt;sup&gt;1,2&lt;/sup&gt;, Mariscal Brice Tchatat Tali&lt;sup&gt;2&lt;/sup&gt;, Florence Ngueguim Tsofack&lt;sup&gt;1&lt;/sup&gt;, Théophile Dimo&lt;sup&gt;1&lt;/sup&gt;, Fabrice Fekam Boyom&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Animal Biology and Physiology, University of Yaoundé 1, P.O. Box 812, Yaounde, CAMEROON.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biochemistry, Faculty of Science, University of Yaoundé 1, P.O. Box 812, Yaoundé, CAMEROON.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biochemistry, Faculty of Science, University of Bamenda, P.O. Box 39, Bamenda, CAMEROON.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmaceutical Sciences, University of Dschang, P.O. Box 67, Dschang, CAMEROON.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Malatee Tayeh</style></author><author><style face="normal" font="default" size="100%">Poonsit Hiransai</style></author><author><style face="normal" font="default" size="100%">Hathaichanok Kommen</style></author><author><style face="normal" font="default" size="100%">Ramida Watanapokasin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anti-migration and Anti-invasion Abilities of Methanolic Leaves Extract of Clerodendrum Inerme on Lung Cancer Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-invasion</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-migration</style></keyword><keyword><style  face="normal" font="default" size="100%">Clerodendrum inerme</style></keyword><keyword><style  face="normal" font="default" size="100%">Human lung adenocarcinoma</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1024-1031</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Clerodendrum inerme &lt;/em&gt;is a folk medicinal plant used in the treatment of various illnesses such as a cough, scrofulous infection, venereal infection, skin diseases and tumors. It exhibited many pharmacological effects including hepatoprotective, anti-inflammatory, antibacterial, anti-oxidant and anticancer properties. &lt;strong&gt;Objective: &lt;/strong&gt;The purpose of this study was to investigate the influence of methanolic extract of&lt;em&gt; C. inerme&lt;/em&gt; leaves on migration, invasion and adhesion activities on human lung adenocarcinoma. &lt;strong&gt;Materials and methods:&lt;/strong&gt; Cytotoxicity, cell motility, migration, invasion and adhesion abilities were detected by MTT, wound healing, trans-well mobilization, modified Boyden chamber and cell adhesion assay, respectively. &lt;strong&gt;Results: &lt;/strong&gt;The results demonstrated that up to 400 μg/mL methanolic leaves extract has low toxicity on A549 cells showing more than 50% cell viability. At non-cytotoxic and sub-toxic doses (200 and 400 μg/mL) of methanolic leave extract significantly suppressed cell motility, migration, invasion and cell adhesion compared with the untreated control. &lt;strong&gt;Conclusion:&lt;/strong&gt; These results suggested that methanolic leaves extract of &lt;em&gt;C. inerme &lt;/em&gt;inhibited migration, invasion and adhesion of A549 cells. These findings showed new therapeutic potential for &lt;em&gt;C. inerme&lt;/em&gt; in anti-metastatic therapy.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1024</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Malatee Tayeh&lt;sup&gt;1,&lt;/sup&gt;*, Poonsit Hiransai&lt;sup&gt;1&lt;/sup&gt;, Hathaichanok Kommen&lt;sup&gt;2&lt;/sup&gt;, Ramida Watanapokasin&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;School of Allied Health Sciences, Walailak University, Nakhon Si Thammarat 80160, THAILAND.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;School of Sciences, Walailak University, Nakhon Si Thammarat 80160, THAILAND.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biochemistry, Faculty of Medicine, Srinkharinwirot University, Bangkok 10110, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Muhammad Almurdani</style></author><author><style face="normal" font="default" size="100%">Adel Zamri</style></author><author><style face="normal" font="default" size="100%">Titania T Nugroho</style></author><author><style face="normal" font="default" size="100%">Jasril Karim</style></author><author><style face="normal" font="default" size="100%">Yum Eryanti</style></author><author><style face="normal" font="default" size="100%">Rudi Hendra</style></author><author><style face="normal" font="default" size="100%">Hilwan Yuda Teruna</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antioxidant and Antidiabetic Activities of Mempening (Lithocarpus bancanus) Leaves</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antidiabetic</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Lithocarpus bancanus</style></keyword><keyword><style  face="normal" font="default" size="100%">Talang Mamak Tribe</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">328-334</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Lithocarpus bancanus &lt;/em&gt;or commonly called as mempening in Talang Mamak Tribe, Indonesia is a plant that is used as a traditional medicine.&lt;strong&gt; Objective: &lt;/strong&gt;This study aim to evaluated antioxidant and antidiabetic activities of &lt;em&gt;L. bancanus&lt;/em&gt; leaves extract. &lt;strong&gt;Material and Methods:&lt;/strong&gt; The methanol extract was obtained by maceration of the leaves. The n-hexane, dichloromethane and ethyl acetate fractions were prepared by successive partition process of the methanol extract. Antioxidant activities were evaluated by various antioxidant assays, including DPPH (1,1-diphenyl-2-picrylhydrazyl), FRAP (ferric reducing antioxidant power), CUPRAC (&lt;em&gt;cupric reducing antioxidant capacity&lt;/em&gt;), and ABTS (&lt;em&gt;2,2’-azonobis 3-ethylbenzothiazoline-6-sulfonic acid&lt;/em&gt;) method. Total phenolics were estimated based on the Folin–Ciocalteu method, while, aluminum chloride methods were employed to estimate total flavonoids. Antidiabetic activies was determined by inhibiting the activity of α-glucosidase method. Results: antioxidant activity assay against DPPH radical as well as the total phenolic and flavonoid content of &lt;em&gt;L. bancanus&lt;/em&gt; leaves showed that the methanol extract possessed IC&lt;sub&gt;50&lt;/sub&gt; value of 39.469 ± 0.273 μg/mL with total phenol and flavonoid were 11.426 ± 0.432 mg GAE/g dry weight sample and 15.423 ± 0.213 mg QE/g respectively. The FRAP, CUPRAC and ABTS values of methanol extract were 3494.302 ±0.456, 26665.501 ± 5.940 and 2857.977 ± 0.715 μM TE/g dry weight sample respectively. Antidiabetic activity of methanol extract with IC&lt;sub&gt;50&lt;/sub&gt; value of 30.565 ± 0.331 μg/mL. Conclusion: It could be concluded that leaves of &lt;em&gt;L. bancanus&lt;/em&gt; have antioxidant and antidiabetic properties.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">328</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Muhammad Almurdani&lt;sup&gt;1&lt;/sup&gt;, Adel Zamri&lt;sup&gt;1&lt;/sup&gt;, Titania T. Nugroho&lt;sup&gt;1&lt;/sup&gt;, Jasril Karim&lt;sup&gt;1&lt;/sup&gt;, Yum Eryanti&lt;sup&gt;1&lt;/sup&gt;, Rudi Hendra&lt;sup&gt;1&lt;/sup&gt;, Hilwan Yuda Teruna&lt;sup&gt;1,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Riau, Pekanbaru 28293, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">S Suman</style></author><author><style face="normal" font="default" size="100%">SV Suresh Kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antiurolithiatic Activity of Ethanolic Extract of Piper cubeba Dried Fruits: An in-vitro and in-vivo Study</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">calcium oxalate</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethylene glycol</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">HPTLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Terpenoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Urolithiasis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1289-1296</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Piper cubeba &lt;/em&gt;is a well-known traditional plant used in unani medicine belonging to the Piperaceae family and has been examined for the treatment of urolithiasis produced by calcium oxalate.&lt;strong&gt; Methods: &lt;/strong&gt;Ethanolic extract of &lt;em&gt;Piper cubeba &lt;/em&gt;(&lt;em&gt;EEPC&lt;/em&gt;) dried fruits was subjected to phytochemical analysis and HPTLC fingerprinting. An in vitro antiurolithiatic analysis took place through conductometric titrations of CaCl&lt;sub&gt;2&lt;/sub&gt; with Na&lt;sub&gt;2&lt;/sub&gt;C&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt;. Acute toxicity studies conducted as per OECD guidelines. Urolithiasis was established in rats by supplementing 28 days with 0.75% ethylene glycol in the ingesting water. Beside ethylene glycol, &lt;em&gt;EEPC&lt;/em&gt; (100, 200 and 400 mg/kg) was given orally from 15 - 28 days, serum and urine were collected from individual animals and biochemical parameters like BUN, creatinine along with uric acid in serum as well as calcium, oxalate and phosphate in urine the kidney homogenate have been measured on 28&lt;sup&gt;th&lt;/sup&gt; day. Kidney sections have been organized and histopathologically tested for calcium oxalate crystals. &lt;strong&gt;Results:&lt;/strong&gt; Phytochemical analysis of &lt;em&gt;EEPC &lt;/em&gt;disclose the presence of phenolics, tannins, steroids, terpenoids and flavonoids and HPTLC fingerprinting shows the presence of 7 terpenoids, 2 flavonoids when scanned at 540nm and 366nm. &lt;em&gt;In vitro &lt;/em&gt;studies showed reduction in CaOx crystal aggregation and promoted nucleation after treatment with&lt;em&gt; EEPC&lt;/em&gt;.&lt;em&gt; In vivo &lt;/em&gt;studies also showed reduction in elevated levels of serum creatinine, BUN, uric acid, and levels of calcium, oxalate and phosphate in urine and kidney homogenate as compared to disease control rats. The results were supported by histopathological studies.&lt;strong&gt; Conclusion: &lt;/strong&gt;The EEPC have shown significant antiurolithiatic activity by reducing calculi.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1289</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;S. Suman&lt;sup&gt;1,&lt;/sup&gt;*, S.V. Suresh Kumar&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Research Scholar, Jawaharlal Nehru technological University Anantapur, Ananthapuramu-515002, Andhra Pradesh, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacognosy, Creative Educational Society’s college of Pharmacy, NH-7, Chinnatekur, Kurnool-518218, Andhra Pradesh, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Faiza MOULAI-HACENE</style></author><author><style face="normal" font="default" size="100%">Mokhtaria Yasmina BOUFADI</style></author><author><style face="normal" font="default" size="100%">Soumia KEDDARI</style></author><author><style face="normal" font="default" size="100%">Abdelkader HOMRANI</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chemical Composition and Antimicrobial Properties of Elettaria cardamomum Extract</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimicrobial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Chemical composition</style></keyword><keyword><style  face="normal" font="default" size="100%">Elettaria cardamomum</style></keyword><keyword><style  face="normal" font="default" size="100%">Pathogenic strains</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1058-1063</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Cardamom, also known as&lt;em&gt; Elettaria cardamomum,&lt;/em&gt; a venerated perennial herb like the &quot;Queen of Spices&quot; belongs to the Zingiberaceae family. She holds various pharmacological activities due to its phytochemicals it contains such as; phenols, tannins, terpenoids, flavonoids, sterols. &lt;strong&gt;Methods: &lt;/strong&gt;The study included the determination of the chemical composition of&lt;em&gt; Elettaria cardamomum&lt;/em&gt; ethanolic extract (EEC) by HPLC/UV and evaluated their antimicrobial potential against ten pathogenic reference strains using two complementary techniques: the method of diffusion from solid discs and the determination of minimum inhibitory concentrations (MIC). &lt;strong&gt;Results:&lt;/strong&gt; The results obtained from chemical identification of the EEC showed the presence of polyphenolic acids (rosmarinic acid, caffeic acid, ferulic acid, etc.) and many flavonoids (kaempferol, chrysin, galangin, pinocembrine, quercetin, etc.). The results of the antimicrobial effect showed that the extract reacted positively on almost all the microbial strains tested. The EEC extract significantly inhibited the growth of microbial strains, with a broader antimicrobial spectrum with extensive action with inhibitory zones between 8 and 33 mm in diameter. Thus, this extract revealed a dose-dependent antimicrobial activity on these microbial strains used. However, the inhibitory potential of the cardamom extract was variable compared to their MIC ranging from 6.25 to 12.5 mg of dry extract/mL. Therefore, the strains least susceptible to EEC are &lt;em&gt;Bacillus subtilis, Escherichia coli, Aspergillus niger&lt;/em&gt; and&lt;em&gt; Candida albicans&lt;/em&gt;. &lt;strong&gt;Conclusion: &lt;/strong&gt;This activity is due to the phenolic compounds produced by the EEC extract. This extract can be used for the development of plant medicines against microbial infections and fungal infestations.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1058</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Faiza MOULAI-HACENE&lt;sup&gt;1&lt;/sup&gt;, Mokhtaria Yasmina BOUFADI&lt;sup&gt;2,3,&lt;/sup&gt;*, Soumia KEDDARI&lt;sup&gt;2&lt;/sup&gt;, Abdelkader HOMRANI&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Laboratory of Sciences and Techniques of Animal Production (LSTPA), Faculty of Natural Sciences and Life, Abdelhamid Ibn Badis University, Mostaganem, ALGERIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Laboratory of Beneficial Microorganisms, Functional Food and Health (LMBAFS), Faculty of Natural Sciences and Life, Abdelhamid Ibn Badis University, Mostaganem, ALGERIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Laboratory of Pharmaceutical Chemistry, Faculty of Pharmacy, Université Libre de Bruxelles, Brussels, BELGIUM.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Phakamani Hopewell Tsilo</style></author><author><style face="normal" font="default" size="100%">Sidney Tsolanku Maliehe</style></author><author><style face="normal" font="default" size="100%">Jabulani Siyabonga Shandu</style></author><author><style face="normal" font="default" size="100%">Rene Khan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chemical Composition and Some Biological Activities of the Methanolic Encephalartos ferox Fruit Extract</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-quorum sensing</style></keyword><keyword><style  face="normal" font="default" size="100%">Antibacterial</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1190-1197</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Although literature reports the therapeutic properties of &lt;em&gt;Encephalartos ferox&lt;/em&gt;, there are limited pharmacological studies of its fruit. &lt;strong&gt;Objective: &lt;/strong&gt;This study sought to evaluate the antibacterial, antioxidant, anti-quorum sensing and &lt;em&gt;in vitro &lt;/em&gt;cytotoxic activities of the methanolic&lt;em&gt; E. ferox&lt;/em&gt; fruit extract. &lt;strong&gt;Methods: &lt;/strong&gt;The chemical constituent of the methanolic fruit extract was analysed using gas chromatography-mass spectrometry. Antibacterial activity of the extract was investigated against &lt;em&gt;Staphylococcus aureus &lt;/em&gt;(ATCC 25923), &lt;em&gt;Bacillus cereus&lt;/em&gt; (ATCC 10102), &lt;em&gt;Escherichia coli &lt;/em&gt;(ATCC 25922) and &lt;em&gt;Pseudomonas aeruginosa&lt;/em&gt; (ATCC 27853) using the broth dilution method. The standard 2.2-diphenyl-1-picrylhydrazyl (DPPH) and 2.2-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) methods were used to evaluate the scavenging activities of the extract. Anti-quorum sensing activity was assessed against biosensor strain- &lt;em&gt;Chromobacterium violaceum &lt;/em&gt;(ATCC 12472). Cytotoxicity in HepG2 cells was investigated using the tetrazolium-based colorimetric (MTT) assay. &lt;strong&gt;Results: &lt;/strong&gt;The extract revealed eight volatile compounds with cis-Vaccenic acid (87.06%) and 9-Octadecenoic acid, 1,2,3-propanetriyl ester (5.21%) as the major components. Antibacterial activity against all tested strains with minimum inhibitory concentration range of 1.56 - 12.5 mg/mL was observed. The DPPH and ABTS assays demonstrated scavenging activities with the median inhibitory concentration (IC&lt;sub&gt;50&lt;/sub&gt;) values of 0.09 mg/mL and 0.003 mg/mL, respectively. The extract also displayed strong anti-quorum sensing activity with 93% inhibition of violacein production at 25 mg/mL. A half maximum inhibitory concentration (IC&lt;sub&gt;50&lt;/sub&gt;) of 5370 μg/mL was computed in HepG2 cells. &lt;strong&gt;Conclusion:&lt;/strong&gt; The extract has potential to be used as a source of therapeutic compounds in pharmaceutical applications.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">1190</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Phakamani Hopewell Tsilo&lt;sup&gt;1,&lt;/sup&gt;*, Sidney Tsolanku Maliehe&lt;sup&gt;1&lt;/sup&gt;, Jabulani Siyabonga Shandu&lt;sup&gt;1&lt;/sup&gt;, Rene Khan&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biochemistry and Microbiology, University of Zululand, KwaDlangezwa 3886, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Discipline of Medical Biochemistry, College of Health Sciences, University of KwaZulu- Natal, Private Bag X 54001, Durban 4000, SOUTH AFRICA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Srikalyani V</style></author><author><style face="normal" font="default" size="100%">Ilango K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chemical Fingerprint by HPLC-DAD-ESI-MS, GC-MS Analysis and Anti-Oxidant Activity of Manasamitra Vatakam: A Herbomineral Formulation</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Classical formulation</style></keyword><keyword><style  face="normal" font="default" size="100%">Diffusion and dilution methods</style></keyword><keyword><style  face="normal" font="default" size="100%">Heavy metals</style></keyword><keyword><style  face="normal" font="default" size="100%">MIC</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February  2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">115-123</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Manasamitra Vatakam is a classical ayurvedic herbo mineral formulation used for the treatment of neurodegerative properties and epileptic disorders. The wide range mixture of herbal extracts and minerals were used in the formulation. &lt;strong&gt;Aim:&lt;/strong&gt; The aim of the study implies in performing the chemo-profiling, chromatographic fingerprint analysis by HPLC-DAD-ESI-MS for the selected formulations of Manasamitra Vatakam followed by the identification of bioactive compounds by Gas Chromatography – Mass Spectrometric (GC-MS) analysis, to evaluate the diffusion and dilution methods for the determination of anti-bacterial activity in the methanolic extracts of Manasamitra Vatakam (MMV). &lt;strong&gt;Materials and Methods: &lt;/strong&gt;The antibacterial activity was performed by both diffusion and dilution methods whereas the antioxidant activity was performed by free radical scavenging of 2,2-diphenyl-1-picrylhydrazy and hydrogen peroxide scavenging assay method. &lt;strong&gt;Results:&lt;/strong&gt; The estimation of bioactive constituents showed positive results by qualitative analysis. Antibacterial activity of MMV was evaluated against two-gram positive &lt;em&gt;Staphylococcus aureus&lt;/em&gt; and &lt;em&gt;Bacillus cereus&lt;/em&gt;, two gram negative &lt;em&gt;Escherichia coli &lt;/em&gt;and&lt;em&gt; Klebsiella pneumonia &lt;/em&gt;by disk diffusion (0.078-10μg mL&lt;sup&gt;-1&lt;/sup&gt;), broth dilution (0.078-10μg mL&lt;sup&gt;-1&lt;/sup&gt;) and broth micro dilution method (0.39-50μg mL&lt;sup&gt;-1&lt;/sup&gt;) respectively. The bioactive constituents were analysed by GC-MS analysis for the methanolic extract of the formulation. &lt;strong&gt;Conclusion:&lt;/strong&gt; To conclude, the formulation was found abundant with phenolic and flavonoid compounds by HPLC-ESI-MS analysis, the bioactive compounds identified are responsible for the anti-bacterial activity. The broth microdilution method performed by resazurin method was observed as the fast screening, sensitive and accurate method for the quantitative determination of antibacterial activity.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">115</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Srikalyani V&lt;sup&gt;1&lt;/sup&gt;, Ilango K&lt;sup&gt;1,2,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Analytical Chemistry, Interdisciplinary Institute of Indian System of Medicine (IIISM), SRM Institute of Science and Technology, Kattankulathur- 603 203, Kancheepuram (Dt), Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Chemistry, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur-603 203, Kancheepuram (Dt), Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Manish Kumar</style></author><author><style face="normal" font="default" size="100%">Ankita Misra</style></author><author><style face="normal" font="default" size="100%">Akanksha Srivastava</style></author><author><style face="normal" font="default" size="100%">Pushpendra Kumar Shukla</style></author><author><style face="normal" font="default" size="100%">L M Tewari</style></author><author><style face="normal" font="default" size="100%">Sharad Srivastava</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Pharmacognostical and Pharmacological Evaluation of Costus speciosus (Koen) J.E. Sm. Germplasm Collected from Eastern Ghats of India</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-diabetic</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory</style></keyword><keyword><style  face="normal" font="default" size="100%">Costus speciosus</style></keyword><keyword><style  face="normal" font="default" size="100%">Diosgenin</style></keyword><keyword><style  face="normal" font="default" size="100%">HPTLC</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February  2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">150-156</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Costus speciosus &lt;/em&gt;is an erect perennial herb belonging to family Costaceae, an important medicinal plant widely used in several indigenous medicinal formulations. &lt;strong&gt;Objective: &lt;/strong&gt;A comparative evaluation of Pharmacognostical and Pharmacological potential of &lt;em&gt;Costus speciosus &lt;/em&gt;for the validation of traditional claims and quality parameters for industry. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Pharmacognostical studies were performed as per Ayurvedic Pharmacopeia of India and quantification of diosgenin was done through HPTLC. &lt;em&gt;In vitro&lt;/em&gt; antidiabetic activity was evaluated by α-amylase inhibition assay based on starch iodine method and &lt;em&gt;in vitro &lt;/em&gt;anti-inflammatory were done by using inhibition of protein denaturation assay. &lt;strong&gt;Results: &lt;/strong&gt;The pharmacognostical standards were also laid down for each sample. Morpho-anatomical characters had no distinct variation in all the collected samples of Eastern Ghats. The quantification of diosgenin (without hydrolysis of samples) in the collected germplasm varies significantly from 0.002 to 0.076 % on dry weight basis. The maximum content was recorded in NBCS-06 from Patiya, Bhubaneswar and was identified as distinct chemotype with high metabolite content. IC&lt;sub&gt;50&lt;/sub&gt; value of&lt;em&gt; Costus speciosus &lt;/em&gt;extract in starch-iodine assay was found to be maximum in NBCS- 6 (87.54 μg/ml) and inhibition of protein denaturation assay was found to be maximum in NBCS- 11 (73.91 μg/ml), respectively. &lt;strong&gt;Conclusion: &lt;/strong&gt;The study suggests that the &lt;em&gt;Costus speciosus&lt;/em&gt; germplasm possess potential anti-inflammatory and anti-diabetic activity and comparative pharmacognostical parameters will be useful in collection of location specific potential samples for industrial usage along with quality control of raw materials.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">150</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Manish Kumar&lt;sup&gt;1,2&lt;/sup&gt;, Ankita Misra&lt;sup&gt;1&lt;/sup&gt;, Akanksha Srivastava&lt;sup&gt;1&lt;/sup&gt;, Pushpendra Kumar Shukla&lt;sup&gt;1&lt;/sup&gt;, L. M. Tewari&lt;sup&gt;2&lt;/sup&gt;, Sharad Srivastava&lt;sup&gt;1,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Pharmacognosy Division, CSIR-National Botanical Research Institute, Lucknow (U.P.) 226001, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Botany, D.S.B. Campus, Kumaun University, Nainital-263002, Uttarakhand, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nandhini S</style></author><author><style face="normal" font="default" size="100%">Ilango K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Study on Pharmacognostical, Phytochemical Investigations and Quantification of Vasicine Content in the Extracts of Adhatoda vasica Nees and Adhatoda beddomei CB Clarke</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adhatoda beddomei</style></keyword><keyword><style  face="normal" font="default" size="100%">Adhatoda vasica</style></keyword><keyword><style  face="normal" font="default" size="100%">HPTLC fingerprint</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognosy</style></keyword><keyword><style  face="normal" font="default" size="100%">Vasicine</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">884-896</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Adhatoda, a perennial shrub of family Acanthaceae are well-known medicinal plant for the treatment and management of respiratory disorders such as asthma and bronchitis. &lt;em&gt;Adhatoda vasica &lt;/em&gt;and&lt;em&gt; Adhatoda beddomei&lt;/em&gt; are the species of Adhatoda, has been widely used in Indian system of medicine. Although, phytochemical and pharmacological investigations were reported on &lt;em&gt;A. vasica, &lt;/em&gt;there has been comparative investigations on different Adhatoda species are lacking. &lt;strong&gt;Objective:&lt;/strong&gt; The study was undertaken to compare the pharmacognostical and phytochemical parameters of two species of Adhatoda for rapid identification and authentication of the plants. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Pharmacognostical features were studied by macroscopic, microscopic studies and physicochemical analysis such as determination of foreign matter, ash value, extractive value and loss on drying. Phytochemical investigations were analysed using phytochemical screening, bioactive content determination, HPTLC fingerprint analysis and estimation of vasicine content by HPLC analysis. &lt;strong&gt;Results: &lt;/strong&gt;Microscopic study differentiated the pharmacognostical features between two species by demonstrating the anatomical characteristics. Powder microscopy of &lt;em&gt;A. vasica&lt;/em&gt; revealed the presence of diacytic stomata, glandular and non-glandular trichomes whereas rod shaped crystals were seen only in &lt;em&gt;A. beddomei. &lt;/em&gt;Qualitative and quantitative phytochemical investigations revealed the presence and estimation of various phytoconstituents in both the species. HPTLC fingerprint profiling evaluated the number of constituents present in the extracts and HPLC analysis revealed high content of vasicine in&lt;em&gt; A. vasica&lt;/em&gt; extracts when compared to &lt;em&gt;A. beddomei.&lt;strong&gt; &lt;/strong&gt;&lt;/em&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; The present study provides the useful information to differentiate the plant species and can serve as a diagnostic tool for the standardization and identification of adulterant in the crude drug market.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">884</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nandhini S&lt;sup&gt;1&lt;/sup&gt;, Ilango K&lt;sup&gt;1,2,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Pharmacognosy and Phytochemistry, Interdisciplinary Institute of Indian System of Medicine (IIISM), SRM Institute of Science and Technology, Kattankulathur - 603 203, Chengalpattu (Dt), Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Chemistry, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur- 603 203, Chengalpattu (Dt), Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Iman AA Kassem</style></author><author><style face="normal" font="default" size="100%">Ayman A Farghaly</style></author><author><style face="normal" font="default" size="100%">Neveen S Ghaly</style></author><author><style face="normal" font="default" size="100%">Zeinab M Hassan</style></author><author><style face="normal" font="default" size="100%">Marian Nabil</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Composition and Genoprotective Effect of the Flavonoidal Content of Lepidium sativum L. Methanolic Seed Extract against Cyclophosphamide- Induced DNA Damage in Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Chromosomal abberations</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Lipidium sativum</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February  2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">124-130</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Lepidium sativum&lt;/em&gt; L. (Family Brassicaceae) is known to possess different pharmacological properties. &lt;strong&gt;Objective: &lt;/strong&gt;The genoprotective role of flavonoids of &lt;em&gt;L. sativum &lt;/em&gt;methanolic seed extract (LSF) against cyclophosphamide (CP)-induced DNA damage, in somatic and germ cells of mice, as well as characterization of the flavonoidal content were carried out in this study. Chromosomal aberration analysis in somatic and germ cells were also included. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Six mice groups were used for this study. Group 1 served as a negative control. Group 2 received oral LSF (100 mg/kg b.wt.) for 5 consecutive days. Group 3 served as a positive control by receiving a single intraperitoneal (i.p.) CP dose (20 mg/kg b.wt.). The three other groups were orally administered 25, 50 and 100 mg/kg b.wt. LSF, respectively, for 5 consecutive days. On the last day of treatment, the three groups received i.p. injection of CP (20 mg/kg b.wt.). Flavonoids were identified using spectral analysis.&lt;strong&gt; Results: &lt;/strong&gt;LSF inhibited DNA aberrations in mice caused by cyclophosphamide dose dependently in the three groups with significant difference in the two groups that received doses of 50 and 100 mg/kg b.wt. The chromosomal aberrations inhibitory indices were calculated as 18 and 31 in mice somatic cells and 27 and 48 in germ cells, respectively. LSF was found to contain the flavonoids kaempferol, quercetin, kaempferol-3-O-α-L-rhamnopyranoside, kaempferol-3-O-β-D-glucopyranoside, and quercetin-3-O-β-D-galactopyranoside. &lt;strong&gt;Conclusion: &lt;/strong&gt;LSF inhibited the DNA damage induced by CP in somatic and germ cells of mice dose-dependently. The antioxidant properties associated with flavonoids might account for the genoprotective activity.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">124</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Iman AA Kassem&lt;sup&gt;1,&lt;/sup&gt;*, Ayman A Farghaly&lt;sup&gt;2&lt;/sup&gt;, Neveen S Ghaly&lt;sup&gt;1&lt;/sup&gt;, Zeinab M Hassan&lt;sup&gt;1&lt;/sup&gt;, Marian Nabil&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Chemistry of Natural Compounds Department, National Research Centre, Dokki 12622, Giza, EGYPT.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Genetics and Cytology Department, National Research Centre, Dokki 12622, Giza, EGYPT.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nanthakarn Woottisin</style></author><author><style face="normal" font="default" size="100%">Sumet Kongkiatpaiboon</style></author><author><style face="normal" font="default" size="100%">Sophida Sukprasert</style></author><author><style face="normal" font="default" size="100%">Korbtham Sathirakul</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Development and Validation of Stability Indicating HPLC Method for Determination of Caffeic Acid, Vitexin and Rosmarinic Acid in Thunbergia laurifolia Leaf Extract</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Force degradation</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolic compound</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical screening</style></keyword><keyword><style  face="normal" font="default" size="100%">Stabilityindicating method</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">611-618</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;em&gt;Thunbergia laurifolia &lt;/em&gt;has been a popular herb used in Thai traditional medicine for detoxification and as antipyretic. It contains rosmarinic acid (RA), caffeic acid (CA) and vitexin as major compounds. In order to control the herbal quality, the stability indicating high-performance liquid chromatography (HPLC) was developed and validated. The stability study of compounds in &lt;em&gt;T. laurifolia&lt;/em&gt; leaf extract was investigated. The chromatographic separation was performed using a reversed-phase C18 column and mobile phase consisted of 0.5% acetic acid and methanol using a gradient elution with 1.0 mL/min flow rate. The detection wavelength was set at 330 nm. The method was validated for its linearity, precision, accuracy, limit of detection and limit of quantitation. Forced degradation of three compounds in extract showed that they were stable in oxidative condition, but highly labile under alkaline hydrolytic conditions. All three compounds in &lt;em&gt;T. laurifolia &lt;/em&gt;leaf extract were stable at room temperature at least 3 months while a remarkable decrease of RA, vitexin and CA in the extract were found in accelerated condition. This finding could be applied for predicting the storage recommendation and expiry of&lt;em&gt; T. laurifolia&lt;/em&gt; extract and its related pharmaceutical products.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">611</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nanthakarn Woottisin&lt;sup&gt;1&lt;/sup&gt;, Sumet Kongkiatpaiboon&lt;sup&gt;2&lt;/sup&gt;, Sophida Sukprasert&lt;sup&gt;1,3,&lt;/sup&gt;*, Korbtham Sathirakul&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Integrative Medicine, Chulabhorn International College of Medicine, Thammasat University (Rangsit Campus), Pathum Thani 12120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Drug Discovery and Development Center, Office of Advanced Science and Technology, Thammasat University (Rangsit Campus), Pathum Thani 12120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Protein and Proteomics Research Center for Commercial and Industrial Purposes (ProCCI), Khon Kaen University, Khon Kaen 40002, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok 10400, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sundarapandian Subramanian</style></author><author><style face="normal" font="default" size="100%">Mohammed Junaid Hussain Dowlath</style></author><author><style face="normal" font="default" size="100%">Sathish Kumar Karuppannan</style></author><author><style face="normal" font="default" size="100%">Saravanan M</style></author><author><style face="normal" font="default" size="100%">Kantha Devi Arunachalam</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Solvent on the Phytochemical Extraction and GC-MS Analysis of Gymnema sylvestre</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chromatography</style></keyword><keyword><style  face="normal" font="default" size="100%">Cold maceration</style></keyword><keyword><style  face="normal" font="default" size="100%">Gymnema sylvestre</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal plants</style></keyword><keyword><style  face="normal" font="default" size="100%">plant constituents</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">749-761</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;The medicinal plant &lt;em&gt;Gymnema sylvestre&lt;/em&gt; found in the Indian subcontinent and Srilanka is known for its anti-diabetic, diuretic, anti-obesity, anti-cancer, antimicrobial, anti-inflammatory properties. The current study is focused on the phyto compound extraction efficiency of different solvents like ethanol, methanol, ethyl acetate, hexane, benzene and chloroform by gas chromatography–mass spectrometry analysis of &lt;em&gt;Gymenma sylvestre. &lt;/em&gt;From the results, it is concluded that &lt;em&gt;G. sylvestre&lt;/em&gt; leaves extracts contains more than 38 phyto compounds with natural antioxidants potential. Further analysis of the extract will help in identifying the effective compounds which can be of potent use in the pharmacological field.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">749</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sundarapandian Subramanian&lt;sup&gt;1&lt;/sup&gt;, Mohammed Junaid Hussain Dowlath&lt;sup&gt;1&lt;/sup&gt;, Sathish Kumar Karuppannan&lt;sup&gt;1&lt;/sup&gt;, Saravanan M&lt;sup&gt;2&lt;/sup&gt;, Kantha Devi Arunachalam&lt;sup&gt;1,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Center for Environmental Nuclear Research, Directorate of Research, SRM Institute of Science and Technology, Kattankulathur, Chennai 603203, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biotechnology, School of Bioengineering, SRM Institute of Science and Technology, Kattankulathur, Chennai 603203, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohammed Junaid Hussain Dowlath</style></author><author><style face="normal" font="default" size="100%">Sathish Kumar Karuppannan</style></author><author><style face="normal" font="default" size="100%">Darul Raiyaan GI</style></author><author><style face="normal" font="default" size="100%">Mohamed Khalith SB</style></author><author><style face="normal" font="default" size="100%">Sundarapandian Subramanian</style></author><author><style face="normal" font="default" size="100%">Kantha Deivi Arunachalam</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Solvents on Phytochemical Composition and Antioxidant Activity of Cardiospermum halicacabum (L.) Extracts</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cardiospermum halicacabum</style></keyword><keyword><style  face="normal" font="default" size="100%">Cold maceration</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal plants</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword><keyword><style  face="normal" font="default" size="100%">Radical scavenging activity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1241-1251</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Cardiospermum halicacabum&lt;/em&gt; (&lt;em&gt;C. halicacabum&lt;/em&gt;) is a common medicinal herb found in India and other Asian countries. It has various medicinal properties such as antimicrobial, pain relief, antibiotics, anti-inflammatory, antioxidants, anticancer etc. It is commonly used for treating diabetes, arthritis, limbs stiffness, rheumatism, lumbago, earache, fever. Type of solvent and polarity intensively affects the antioxidant activity of the extracts due to the solubility of the phytocompounds such as polyphenols and flavonoids in various solvents.&lt;strong&gt; Materials and Methods: &lt;/strong&gt;In this study, different solvents like, ethanol, methanol, chloroform and petroleum ether were used for the extraction of &lt;em&gt;C. halicacabum&lt;/em&gt;. Cold maceration method was followed for extraction. The crude extracts were screened preliminary and then confirmed using Fourier transform-infrared spectroscopy analysis. Gas chromatography-mass spectrometry was used to determine the chemical composition of each extract. The DPPH (2,2-diphenyl- 1-picrylhydrazyl) method was used for the evaluation of the antioxidant activity of different crude extracts of &lt;em&gt;C. halicacabum.&lt;/em&gt; &lt;strong&gt;Results:&lt;/strong&gt; The results showed that there is significant influence of solvent type in preserving various phytocompounds of the &lt;em&gt;C. halicacabum&lt;/em&gt; leaves extract. The evaluation of the antioxidant capacity of different crude extracts was in the order of ethanol &amp;gt; methanol &amp;gt; petroleum ether &amp;gt; chloroform extract.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1241</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Mohammed Junaid Hussain Dowlath, Sathish Kumar Karuppannan, Darul Raiyaan GI, Mohamed Khalith SB, Sundarapandian Subramanian and Kantha Deivi Arunachalam*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Center for Environmental Nuclear Research, Directorate of Research, SRM Institute of Science and Technology, Kattankulathur- 603203, India.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ratika Rahmasari</style></author><author><style face="normal" font="default" size="100%">Takahiro Haruyama</style></author><author><style face="normal" font="default" size="100%">Muhareva Raekiansyah</style></author><author><style face="normal" font="default" size="100%">Farhana Mossadeque</style></author><author><style face="normal" font="default" size="100%">Marina Ika Irianti</style></author><author><style face="normal" font="default" size="100%">Ayun Erwina Arifianti</style></author><author><style face="normal" font="default" size="100%">Nobuyuki Kobayashi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Establishment of Simple Cell-based Screening Assay and the Identification of Potent Antiviral Activity of a Plant Extract against HSV-1</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">HSV-1</style></keyword><keyword><style  face="normal" font="default" size="100%">Natural product activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Simple cell-based screening</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">251-259</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Backgrounds: &lt;/strong&gt;Drug screening is a time-consuming and costly process confronted with low productivity and challenges in using animals, which limits the discovery of new drugs. The cellbased assay allows the minimization of using the animal models and can provide more relevant &lt;em&gt;in vivo &lt;/em&gt;biological information than biochemical assay. &lt;strong&gt;Objective:&lt;/strong&gt; We aimed to establish a simple cell-based screening assay for the discovery of lead extract against HSV-1. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Assay setting up was performed by optimization of the cell, incubation time, virus titer, and determination of Z value. &lt;strong&gt;Results: &lt;/strong&gt;We have successfully established reproducible methods, by setting up assay plate including determination: 1) Vero cells as a model for HSV-1 infection, 2) Incubation for 5 days as sufficient time for CPE endpoint at monolayer cells, 3) 100 TCID&lt;sub&gt;50&lt;/sub&gt;/well HSV-1 as infection titer which caused high percentage of cell detachment, 4) determination of Z value of 100 TCID&lt;sub&gt;50&lt;/sub&gt;/well infection &amp;gt; 0.5. In addition, the established system was tested using ACV as the most common anti-HSV drug. Furthermore, we demonstrated the current system to screen extracts from &lt;em&gt;Acacia nilotica, Uncaria gambir &lt;/em&gt;and &lt;em&gt;Aspalathus linearis &lt;/em&gt;against HSV-1. It was observed that the alkaline extract of Uncaria gambir exhibited the highest SI (12.5) compared to other extracts. &lt;strong&gt;Conclusion: &lt;/strong&gt;We demonstrated current cellbased screening system was reproducible and able to identify lead extracts against HSV-1 infection.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">251</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ratika Rahmasari&lt;sup&gt;1&lt;/sup&gt;, Takahiro Haruyama&lt;sup&gt;2&lt;/sup&gt;, Muhareva Raekiansyah&lt;sup&gt;3&lt;/sup&gt;, Farhana Mossadeque&lt;sup&gt;4&lt;/sup&gt;, Marina Ika Irianti&lt;sup&gt;1&lt;/sup&gt;, Ayun Erwina Arifianti&lt;sup&gt;1&lt;/sup&gt;, Nobuyuki Kobayashi&lt;sup&gt;2,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Pharmacy, University of Indonesia, Depok, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Central Research Center, AVSS, Okinawa, JAPAN.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;PT Sciencewerke Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Institute of Tropical Medicine, Nagasaki University, Nagasaki, JAPAN.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Retno Susilowati</style></author><author><style face="normal" font="default" size="100%">Lailatul Khoiriyah</style></author><author><style face="normal" font="default" size="100%">Exma Mutatal Hikmah</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Estrogenic Effect of the Leaves from Katuk (Sauropus androgynus L. Merr) on Vaginal and Endometrial Atrophy in Perimenopausal Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Endometrial atrophy</style></keyword><keyword><style  face="normal" font="default" size="100%">Estrogenic effect</style></keyword><keyword><style  face="normal" font="default" size="100%">Laboratory mice</style></keyword><keyword><style  face="normal" font="default" size="100%">Perimenopause</style></keyword><keyword><style  face="normal" font="default" size="100%">S. androgynus leaf extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Vaginal atrophy</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">240-245</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To examine the potency of estrogenic effect of Katuk (or star gooseberry or sweet leaf) &lt;em&gt;Sauropus androgynus&lt;/em&gt; L. Merr (Phyllanthaceae) leaf extract on the vaginal and endometrial atrophy in perimenopausal mice model. &lt;strong&gt;Methods: &lt;/strong&gt;Completely random experiments divided into 4 groups with 5 female mice in each group: control group (N), perimenopause group which induced by 4-vynil cyclohexene dioxide (VCD) (P0), perimenopause group followed by &lt;em&gt;S. androgynus &lt;/em&gt;leaves extract administration with 15 and 30 mg/kg BW (P15 and P30). The mice were induced to artificial perimenopause with 160 mg/kg body weight (BW) of VCD 5 times/week for 2 weeks and continuously treated with &lt;em&gt;S. androgynus&lt;/em&gt; leaf extract for 30 days. Vaginal smear examination, maturation index (MI), vaginal epithelium and endometrial thickness were observed. Data were analyzed using a standard one-way ANOVA with LSD Test by SPSS 16.0 for Windows. &lt;strong&gt;Results: &lt;/strong&gt;Administration of &lt;em&gt;S. androgynus&lt;/em&gt; leaf extract for 30 days to perimenopausal mice model significantly decreased the duration of mice diestrus phase (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.01) compared to perimenopause mice.&lt;em&gt; S. androgynus &lt;/em&gt;leaf extract treatment at dose 30 mg/kg BW led to higher vaginal epithelium thickness and maturation index compared to another group (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.01). The effective dose to enhance the vaginal epithelial and endometrial cells proliferation was 30 mg/ kg BW. &lt;strong&gt;Conclusions:&lt;/strong&gt;&lt;em&gt; S. androgynus&lt;/em&gt; leaf extract had a good estrogenic action that it might be useful for therapy of vaginal and endometrial atrophy caused by perimenopause effect.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">240</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Retno Susilowati*, Lailatul Khoiriyah, Exma Mutatal Hikmah&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Biology, Faculty of Science and Technology, State Islamic University of Maulana Malik Ibrahim Malang, Malang 65144, East Java, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sharada Laxman Deore</style></author><author><style face="normal" font="default" size="100%">Someshekhar S Khadabadi</style></author><author><style face="normal" font="default" size="100%">Bhushan A Baviskar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Expression of Heat-labile Enterotoxin of Escherichia coli in Biolistic Transformed Hairy Roots of Daucus carota L.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Carrot</style></keyword><keyword><style  face="normal" font="default" size="100%">Gene gun</style></keyword><keyword><style  face="normal" font="default" size="100%">hairy root</style></keyword><keyword><style  face="normal" font="default" size="100%">LTB</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1440-1443</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Expression and secretion of recombination proteins in transgenic hairy roots have opened door to simple, feasible and economic option compared to animal and bacterial systems. Here, we report a feasibility study for producing the nontoxic B subunit of Escherichia coli heatlabile enterotoxin (LTB) in &lt;em&gt;Daucus carota&lt;/em&gt; L hairy root where transformation is achieved by biolistic gene gun method. &lt;em&gt;Agrobacterium rhizogenes &lt;/em&gt;strain (R-1000) cells containing synthetic LTB gene in pMYO51T plant expression vector under the CaMV 35S promoter introduced to &lt;em&gt;Daucus carota&lt;/em&gt; L roots by biolistic gene gun method. PCR amplification confirmed the integration of synthetic LTB gene in carrot hairy roots. Western blot analysis confirmed production of LTB pentamer in similar banding pattern to the native bacterial derived LTB. 0.50-0.70% of LTB protein estimated in carrot hairy roots. GM1-ganglioside assay indicated formation of biological active pentamers. LTB protein with biochemical properties identical to native LTB protein in the hairy roots of edible carrot roots opens the way for inexpensive, safe, and effective plant-based edible vaccines for humans and animals.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1440</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sharada Laxman Deore*, Someshekhar S. Khadabadi, Bhushan A. Baviskar &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Govt. College of Pharmacy, Kathora naka, Amravati-444604, MS, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lal Chand Pal</style></author><author><style face="normal" font="default" size="100%">Anil kumar</style></author><author><style face="normal" font="default" size="100%">Veena Pande</style></author><author><style face="normal" font="default" size="100%">Ch V Rao</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hepatoprotective Effect of Bioactive Fraction of Lagerstroemia speciosa (L.) Pers. Bark Against Monosodium Glutamate-Induced Liver Toxicity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Apoptosis</style></keyword><keyword><style  face="normal" font="default" size="100%">Lagerstroemia speciosa</style></keyword><keyword><style  face="normal" font="default" size="100%">Monosodium glutamate</style></keyword><keyword><style  face="normal" font="default" size="100%">Superoxide dismutase</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1630-1640</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; The phenolics and flavanoid enriched bioactive fraction of &lt;em&gt;L. speciosa&lt;/em&gt; bark were reported for its medicinal value in various illness however hepatoprotective activity against monosodium glutamate-induced liver toxicity yet to be reported. &lt;strong&gt;Objective:&lt;/strong&gt; To evaluate the hepatoprotective and antioxidant potential of &lt;em&gt;L. speciosa&lt;/em&gt; bark extract fraction against monosodium glutamate-induced liver toxicity. &lt;strong&gt;Methods: &lt;/strong&gt;The phytochemical constituent of ethyl acetate fraction of &lt;em&gt;L. speciosa&lt;/em&gt; bark extract (LSE) were identified by GC-MS analysis. The antioxidant activity of LSE were analyzed with &lt;em&gt;in-vitro&lt;/em&gt; antioxidant assay and subjected to evaluate hepatoprotective activity against monosodium glutamate induced liver toxicity in rat. &lt;strong&gt;Results:&lt;/strong&gt; LSE evaluated as rich in phenolics and flavonoid content along with potent hepatoprotective activity. GC-MS analysis of bioactive fraction exhibits Palmitic Acid, Octadecanoic acid, 5-methyluridine, catechine, epigallocatechin, and norgestrel as major biologically active phytocompounds. Oral administration of LSE (100 and 200 mg/kg.) declined the elevated levels of the biochemical marker as well as interleukins while enhanced the enzymatic antioxidant activity and reduced the increased level of stress marker (MDA) in monosodium glutamate-induced rats. It also restored the altered expression level of proapoptotic genes, but there is no significant change in the expression level of the anti-apoptotic gene. LSE improved histopathology of the liver through the improvement of hepatocellular architecture, inflammation, and attenuation of vascular and cellular degeneration. &lt;strong&gt;Conclusion:&lt;/strong&gt; The bioactive fraction of &lt;em&gt;L. speciosa&lt;/em&gt; bark was found to exhibit strong antioxidant and hepatoprotection in monosodium glutamate induced liver toxicity in rats.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1630</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Lal Chand Pal&lt;sup&gt;1,2&lt;/sup&gt;, Anil kumar&lt;sup&gt;1,2&lt;/sup&gt;, Veena Pande&lt;sup&gt;2&lt;/sup&gt;, Ch.V. Rao&lt;sup&gt;1,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;CSIR-National Botanical Research Institute, Lucknow, UP, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biotechnology, Kumaun University, Nainital, Uttarakhand- 263001, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Noor Azlina Kamaruding</style></author><author><style face="normal" font="default" size="100%">Noraznawati Ismail</style></author><author><style face="normal" font="default" size="100%">Noormaizura Sokry</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Identification of Antibacterial Activity with Bioactive Compounds from Selected Marine Sponges</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Diethyl ether</style></keyword><keyword><style  face="normal" font="default" size="100%">HPTLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Iotrochota baculifera</style></keyword><keyword><style  face="normal" font="default" size="100%">Minimum inhibitory concentration</style></keyword><keyword><style  face="normal" font="default" size="100%">X. muta</style></keyword><keyword><style  face="normal" font="default" size="100%">Xetospongia exigua</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">493-502 </style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Marine sponges (phylum Porifera) are sessile filter-feeders from the ocean that are becoming the wealthiest sources of pharmacologically active compounds. &lt;strong&gt;Objectives:&lt;/strong&gt; Our objectives are to identify bioactive compounds from marine sponges (&lt;em&gt;Xestospongia exigua, Xestospongia muta&lt;/em&gt;, and &lt;em&gt;Iotrochota baculifera&lt;/em&gt;) and to determine their antibacterial activity. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Methanolic crude extracts were subjected to two-steps fractionation: first, solvent partitioning was conducted using diethyl ether and butanol, followed by column chromatography. The resulting fractions were tested for antibacterial activity against four bacterial strains (&lt;em&gt;Staphylococcus aureus&lt;/em&gt; ATCC 25923,&lt;em&gt; Micrococcus luteus &lt;/em&gt;ATCC 4698, &lt;em&gt;Escherichia coli &lt;/em&gt;ATCC 11775, and &lt;em&gt;Salmonella typhimurium&lt;/em&gt; ATCC 14128). The fractions were subsequently profiled using High-Performance Thin Layer Chromatography (HPTLC), and the component of active sub-fractions (SF) was identified using Gas ChromatographyMass Spectrometry (GC-MS). &lt;strong&gt;Results: &lt;/strong&gt;Although no antibacterial activity was recorded of the methanolic extracts in all marine sponges samples, the response towards diethyl ether extracts of &lt;em&gt;X. exigua &lt;/em&gt;was strong. Out of 17 sub-fractions of diethyl ether profiled, three sub-fractions, i.e. 5, 13, and 14 were active. GC-MS identified five compounds in SF 5, four compounds in SF 13, and three compounds in SF 14. Furthermore, SF 13 and SF 14 could inhibit the growth of all bacteria tested, indicating a broad-spectrum activity. On the contrary, SF 5 showed selective inhibition only to &lt;em&gt;E. coli &lt;/em&gt;and &lt;em&gt;S. typhimurium&lt;/em&gt;, indicating narrow-spectrum activity. &lt;strong&gt;Conclusion: &lt;/strong&gt;Bioactive SF 13 of &lt;em&gt;X. exigua&lt;/em&gt; has a high potential as an antibacterial agent but in vitro assessment such as cytotoxicity against mammalian cell lines is needed to determine the toxicity and drug response.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">493</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Noor Azlina Kamaruding, Noraznawati Ismail*, Noormaizura&amp;nbsp;Sokry &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Institute of Marine Biotechnology, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, MALAYSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Qotrunnada Fithrotunnisa</style></author><author><style face="normal" font="default" size="100%">Ade Arsianti</style></author><author><style face="normal" font="default" size="100%">Gerry Kurniawan</style></author><author><style face="normal" font="default" size="100%">Fona Qorina</style></author><author><style face="normal" font="default" size="100%">Nadzila Anindya Tejaputri</style></author><author><style face="normal" font="default" size="100%">Norma Nur Azizah</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In vitro Cytotoxicity of Hibiscus sabdariffa Linn Extracts on A549 Lung Cancer Cell Line</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">A549 Lung Cancer Cell Line</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Hibiscus sabdariffa Linn</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February  2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">14-19</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Lung cancer is the one of the leading causes of cancer death. However, current treatments for lung cancer are expensive and show negative side effects. Therefore, the study concerning natural anticancer from plants has intensified. &lt;em&gt;Hibiscus sabdariffa&lt;/em&gt; Linn are Indonesian herb plants which have been consumed as a drink, are known to have anticancer activity against several cancer cell lines. However, its potential cytotoxic activity on A549 lung cancer cell line is still unclear. &lt;strong&gt;Objective:&lt;/strong&gt; This study aimed to identify cytotoxic activity of &lt;em&gt;Hibiscus sabdariffa&lt;/em&gt; Linn extracts on A549 lung cancer cell line. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;&lt;em&gt;Hibiscus sabdariffa&lt;/em&gt; Linn flowers from Tangerang, province of Banten, Indonesia, were macerated in three different solvents: ethyl acetate, ethanol, and n-hexane. Afterwards, cytotoxic activity of &lt;em&gt;Hibiscus sabdariffa &lt;/em&gt;Linn extracts on A549 lung cancer cell line were evaluated using MTT assay. There were eight variety of concentration of the extracts, the experiment has been done triplicate for each concentration. The anticancer activity is expressed by IC&lt;sub&gt;50&lt;/sub&gt; value. &lt;strong&gt;Results: &lt;/strong&gt;&lt;em&gt;Hibiscus sabdariffa&lt;/em&gt; Linn extracts in ethanol, ethyl acetate, and n-hexane showed IC&lt;sub&gt;50&lt;/sub&gt; value of 374.01 μg/mL, 719.28 μg/mL, and 906.57 μg/mL respectively, in which indicated weak cytotoxic activity on A549 lung cancer cell line. &lt;strong&gt;Conclusion:&lt;/strong&gt; Ethanol, ethyl acetate, and n-hexane extracts of &lt;em&gt;Hibiscus sabdariffa&lt;/em&gt; Linn are potential to be further developed as natural anticancer agents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">14</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Qotrunnada Fithrotunnisa&lt;sup&gt;1&lt;/sup&gt;, Ade Arsianti&lt;sup&gt;2,3,&lt;/sup&gt;*, Gerry Kurniawan&lt;sup&gt;1&lt;/sup&gt;, Fona Qorina&lt;sup&gt;1&lt;/sup&gt;, Nadzila Anindya Tejaputri&lt;sup&gt;1&lt;/sup&gt;, Norma Nur Azizah&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Medical Student, Department of Medical Chemistry, Faculty of Medicine University of Indonesia, Depok, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medical Chemistry, Faculty of Medicine, University of Indonesia, Depok, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Drug Development Research Cluster, Drug Discovery Division, Indonesia Medical Education and Research Institute (IMERI), Faculty of Medicine, University of Indonesia, Jalan Salemba Raya 6 Jakarta 10430, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Budi Santosa</style></author><author><style face="normal" font="default" size="100%">Budi Santosa</style></author><author><style face="normal" font="default" size="100%">Aprilia Indah Kartika</style></author><author><style face="normal" font="default" size="100%">Fitri Nuroini</style></author><author><style face="normal" font="default" size="100%">Aditya Rahman Ernanto</style></author><author><style face="normal" font="default" size="100%">Annisa Ayuningtyas</style></author><author><style face="normal" font="default" size="100%">Mohd Nazil Salleh</style></author><author><style face="normal" font="default" size="100%">Siti Thomas Zulaikhah</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Isolation, Identification Similarity and Qualitative Expression of Metallothionein Gene in IR-Bagendit Rice (Oryza sativa)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">IR-Bagendit</style></keyword><keyword><style  face="normal" font="default" size="100%">Metal Exposure</style></keyword><keyword><style  face="normal" font="default" size="100%">Metallothionein</style></keyword><keyword><style  face="normal" font="default" size="100%">MTs-like gene</style></keyword><keyword><style  face="normal" font="default" size="100%">Rice</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">709-715</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Metallothionein (MTs) is an enzyme that plays a role in the binding of metals in plants. Various types of rice have been known to contain MTs and IR-Bagendit rice leaves have the highest MTs protein content compared to other rice varieties. However, MTs coding gene in IRBagendit rice variety is still unknown. OsRAC1 gene is reported as the down-regulator of MTs and there is an analogous gene for MTs-like gene using RAP1 and RAP2 primers in various plants. This study aimed to isolate, identification of similarity, and analysis of qualitative expression of MTs gene in IR-Bagendit rice as compared to Inpari, IR-36, and IR-34. The steps of this research were DNA isolation, PCR in OsRAC1 gene, RNA isolation and cDNA reverse transcription using primer RP1 and RP2, and agarose gel electrophoresis. Amplification quality of OsRAC1 gene in IR-Bagendit, Inpari, IR-36, and IR-34 showed the same result. Qualitative expression of MTs by reverse transcription showed that IR-Bagendit has the highest MTs-like gene compared to other samples.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">709</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Budi Santosa&lt;sup&gt;1&lt;/sup&gt;, Sri Darmawati&lt;sup&gt;1&lt;/sup&gt;, Aprilia Indah Kartika&lt;sup&gt;1&lt;/sup&gt;, Fitri Nuroini&lt;sup&gt;1&lt;/sup&gt;, Aditya Rahman Ernanto&lt;sup&gt;1&lt;/sup&gt;, Annisa Ayuningtyas&lt;sup&gt;2&lt;/sup&gt;, Mohd Nazil Salleh&lt;sup&gt;3&lt;/sup&gt;, Siti Thomas Zulaikhah&lt;sup&gt;4,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Medical Laboratory Technology, Faculty of Nursing and Health Science, Universitas Muhammadiyah Semarang, 50273 Semarang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Nutrition Division, Faculty of Nursing and Health Science Universitas Muhammadiyah Semarang, 50273 Semarang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Engineering and Life Sciences, Universiti Selangor, Campus Shah Alam, 40000 Selangor, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Public Health, Faculty of Medicine, Sultan Agung Islamic University, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">S Jagadeep Chandra</style></author><author><style face="normal" font="default" size="100%">Naganagouda V Kote</style></author><author><style face="normal" font="default" size="100%">S Sandya</style></author><author><style face="normal" font="default" size="100%">Sharath Chandra SP</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Lithium Nitrate Induced Biochemical Modifications in catla catla upon Short Term Exposure</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1705-1709</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Alkali metals such as lithium nitrate due to its properties have found their application in industries. However, reports of acute toxicological impact of lithium nitrate on aquatic animals are largely not available in the literature. &lt;strong&gt;Objective: &lt;/strong&gt;With this interest, we have assessed the impact of LiNO&lt;sub&gt;3&lt;/sub&gt; on Catla catla, a freshwater fish widely consumed. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; In this study, LC&lt;sub&gt;50&lt;/sub&gt; of LiNO&lt;sub&gt;3&lt;/sub&gt; was determined to be 5ppm, for 24 h. Following this, 1/10th of the LC50 levels of LiNO&lt;sub&gt;3&lt;/sub&gt; (0.5ppm) was chosen for acute investigation of 96 h. Results: The results demonstrated increase in serum aspartate transaminase (AST), alanine transaminase (ALT) and lactate dehydrogenase (LDH) in treated fish. Further examinations disclosed changes in antioxidant enzyme systems with remarkable changes in the serum catalase (CAT) and superoxide dismutase (SOD) contents, with elevation in malondialdehyde (MDA). The investigation found increased glutamate levels in the brain tissue of treated groups, demonstrating tissue damage. &lt;strong&gt;Conclusion: &lt;/strong&gt;The study underlines the toxicological impact of LiNO&lt;sub&gt;3&lt;/sub&gt; and role of certain potential biomarkers which determine the impact of these toxicants in aquatic environment.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1705</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;S. Jagadeep Chandra&lt;sup&gt;1&lt;/sup&gt;, Naganagouda. V. Kote&lt;sup&gt;2&lt;/sup&gt;, S.Sandya&lt;sup&gt;3&lt;/sup&gt;, Sharath Chandra SP&lt;sup&gt;4,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Microbiology, Faculty of Life Sciences, JSS academy of higher education and research, Mysuru, India.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biochemistry, Maharani`s Science College for Women, Bengaluru, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biochemistry, Government Science College, Hassan, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sunayana Vikhe</style></author><author><style face="normal" font="default" size="100%">Rahul Kunkulol</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Microscopic Investigations and Pharmacognosy of Striga orobanchioides Benth</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Pharmacognosy</style></keyword><keyword><style  face="normal" font="default" size="100%">Stem</style></keyword><keyword><style  face="normal" font="default" size="100%">Striga Orobanchioides</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1325-1331</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; To study delineate Pharmacognosy of the stem of plant S&lt;em&gt;triga Orobanchioides &lt;/em&gt;Benth (Scrophulariaceae), prime plant in Indian system of medicine. A comprehensive account on standardization of herbal drug &lt;em&gt;Striga Orobanchioides&lt;/em&gt; Benth by using microscopic as well as Pharmacognostic parameters. In the field of herbal medicines, the main issues are quality, purity, and effectiveness, as in many cases herbal drugs are knowingly or unknowingly substituted or adulterated with similar species or varieties. &lt;strong&gt;Methods:&lt;/strong&gt; The macroscopy, microscopy, physicochemical analysis, preliminary phytochemical testing of the powder of plant stem and other WHO recommended methods for standardization was done. &lt;strong&gt;Results: &lt;/strong&gt;T S of young as well as old stem was studied. T.S. of the young stem confirmed the presence of thin epidermal layer, fairly wide cortex and thin vascular cylinder having the pith disintegrated or retained as homogeneous parenchymatous tissue. T.S. of the old stem confirmed the presence of cortical cells, parenchyma cells, sclerenchyma cells, vascular tissue. The lower conical part of the stem has epidermis cortical zone and vascular cylinder continued from its wide upper part. The cortical zone consists of parenchymatous ground tissue with sealed masses of sclerenchyma cells. The xylem tissue becomes gradually narrow and thin in the end of the stem. It includes compact radial lines of vessels, filnes and xylem rays. &lt;strong&gt;Conclusion: &lt;/strong&gt;The above parameters, being reported to the first time for the studied plant species, and are significant towards establishing the microscopic and Pharmacognostic standards for future identification and authentication of genuine herbal drug. It can be concluded that the Pharmacognostic outline of&lt;em&gt; Striga Orobanchioides &lt;/em&gt;plant is beneficial in developing standards for quality, purity and sample identification.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1325</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sunayana Vikhe&lt;sup&gt;1,&lt;/sup&gt;*, Rahul Kunkulol&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Pravara Rural College of Pharmacy, Loni, (413736), Maharashtra, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology, Pravara Institute of Medical Sciences, Loni, (413736), Maharashtra, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">S Dhanalakshmi</style></author><author><style face="normal" font="default" size="100%">N Harikrishnan</style></author><author><style face="normal" font="default" size="100%">N Srinivasan</style></author><author><style face="normal" font="default" size="100%">P Pandian</style></author><author><style face="normal" font="default" size="100%">BA Tanisha</style></author><author><style face="normal" font="default" size="100%">M Tharun Kumar</style></author><author><style face="normal" font="default" size="100%">V Lokesh</style></author><author><style face="normal" font="default" size="100%">N Yuvashri</style></author><author><style face="normal" font="default" size="100%">S Supriya</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Perspective Overview on Hygrophila auriculata</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hygrophila auriculata</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacological activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemistry</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1748-1752</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;em&gt;Hygrophila auriculata, &lt;/em&gt;belonging to the family Acanthaceae, is a promising medicinal plant with great economic potential. The medicinal value of &lt;em&gt;H. auriculata&lt;/em&gt; has been appreciated in the ancient medical literature. The plant contains terpenoids, alkaloids, flavonoids, and is traditionally known as an aphrodisiac, renal tonic, and for its health-promoting properties. The plant is cultivated throughout India. However, systematic information on the different aspects of this species is not available. In this review, an attempt has been made to present this information.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">1748</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;S Dhanalakshmi&lt;sup&gt;1,&lt;/sup&gt;*, N Harikrishnan&lt;sup&gt;2&lt;/sup&gt;, N Srinivasan&lt;sup&gt;3&lt;/sup&gt;, P Pandian&lt;sup&gt;4&lt;/sup&gt;, BA Tanisha&lt;sup&gt;5&lt;/sup&gt;, M Tharun Kumar&lt;sup&gt;5&lt;/sup&gt;, V Lokesh&lt;sup&gt;5&lt;/sup&gt;, N Yuvashri&lt;sup&gt;5&lt;/sup&gt;, S Supriya&lt;sup&gt;5&lt;/sup&gt;&lt;/strong&gt;&lt;sup&gt; &lt;/sup&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Faculty of Pharmacy, Dr.M.G.R Educational and Research Institute (Deemed to be Univ),Velappanchavadi, Chennai – 600 077, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Chemistry &amp;amp; Analysis, Faculty of Pharmacy, Dr.M.G.R Educational and Research Institute (Deemed to be Univ),Velappanchavadi, Chennai – 600 077, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacy, Faculty of Engineering and Technology, Annamalai University, Annamalai Nagar, Chidambaram, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacognosy, Faculty of Engineering and Technology, Annamalai University, Annamalai Nagar, Chidambaram, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Pharma buddy, Faculty of Pharmacy, Dr.M.G.R Educational and Research Institute (Deemed to be Univ), Velappanchavadi, Chennai – 600 077, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jaya Kuruvilla</style></author><author><style face="normal" font="default" size="100%">M Anilkumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic and Phytochemical Evaluation of the bark of Grewia tiliifolia Vahl.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Grewia tiliifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognostic studies</style></keyword><keyword><style  face="normal" font="default" size="100%">Physicochemical evaluation</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical screening</style></keyword><keyword><style  face="normal" font="default" size="100%">Quantification of phytoconstituents</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">967-976</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;&lt;em&gt;Grewia tiliifolia &lt;/em&gt;Vahl. is an important ethnomedicinal tree widely distributed in the tropical and sub-tropical areas and has been used as a source of herbal shampoo by the local communities in many places of Kerala, India. It has been routinely used in the traditional Ayurvedic medicines against cough, ulcers, cancer, skin diseases, pruritus, wounds and urinary infections. &lt;strong&gt;Objective:&lt;/strong&gt; The aim of this study was the pharmacognostical standardisation of &lt;em&gt;G. tiliifolia. &lt;/em&gt;Methods: Pharmacognostic evaluation of G.tiliifolia bark was carried out by usual macroscopic and microscopic examinations and phytochemical screening. In addition, the quantification of major phytoconstituents such as alkaloids, flavonoids, phenols, tannins, saponins and carotenoids were carried out by standard procedures which can further throw light on the medicinal use of this ethnobotanically important plant. &lt;strong&gt;Results: &lt;/strong&gt;Anatomical studies revealed the presence of prismatic crystals of calcium oxalate and druses in the stem and bark. Mucilage cavities were observed only in the stem. Histochemical studies revealed that the tissues of phloem parenchyma are the main localising region of various phytoconstituents. The physicochemical examinations along with the estimation of alkaloids, flavonoids, phenols, tannins, saponins and carotenoids will help in setting the pharmacopoeial standards of &lt;em&gt;G.tiliifolia. &lt;/em&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;The present study provides useful information that will help in the exact identification as well as assessment of purity of crude drugs of&lt;em&gt; G.tiliifoia.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">967</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Jaya Kuruvilla&lt;sup&gt;1&lt;/sup&gt;, M. Anilkumar&lt;sup&gt;2,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Botany, St. Xavier’s College, Aluva-683102, Ernakulam, Kerala, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Botany, Union Christian College, Aluva-683102, Ernakulam, Kerala, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sathish Kumar Karuppannan</style></author><author><style face="normal" font="default" size="100%">Mohammed Junaid Hussain Dowlath</style></author><author><style face="normal" font="default" size="100%">Mohamed Khalith SB</style></author><author><style face="normal" font="default" size="100%">Darul Raiyaan GI</style></author><author><style face="normal" font="default" size="100%">Sundarapandian Subramanian</style></author><author><style face="normal" font="default" size="100%">Kantha Deivi Arunachalam</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical and Antibacterial Activity of Cardiospermum halicacabum Against Wound Pathogens</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Cardiospermum halicacabum</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1303-1310</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Plants serve as an important source for curing various medical ailments for a wide variety of human and animal diseases. It is therefore necessary to prove the biological activities of the selected plants scientifically using modern technology. The current study focuses on the use of &lt;em&gt;Cardiospermum halicacabum &lt;/em&gt;in their wound healing applications. &lt;em&gt;Cardiospermum halicacabum&lt;/em&gt; is a well-known plant that has antibacterial, anti-inflammatory, anti-rheumatic properties and it is also used to treat joint pains, muscle tears, back pain, etc. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; In this study methanolic extracts of the active compounds from &lt;em&gt;Cardiospermum halicacabum &lt;/em&gt;were tested for its phytochemical attributes by qualitative method, GC-MS, and the antioxidant properties were also assessed. The bactericidal activity and Minimal Inhibitory concentration (MIC) of the plant extract has been evaluated in both Gram +ve and Gram -ve microorganisms using the disc diffusion method. &lt;strong&gt;Results:&lt;/strong&gt; The results obtained showed the presence of significant antibacterial and antioxidant activity. The plant extract was found to be more active against Gram positive microbes compared to Gram negative microbes. The extract has the radical scavenging activity of about 77%. And the GCMS results showed the presence of different phytocompounds which are greatly known for their pharmacognistic activities.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1303</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sathish Kumar Karuppannan, Mohammed Junaid Hussain Dowlath, Mohamed Khalith S B, Darul Raiyaan G I, Sundarapandian Subramanian, Kantha Deivi Arunachalam* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Center for Environmental Nuclear Research, Directorate of Research, SRM Institute of Science and Technology, Kattankulathur-603203, India.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ade Arsianti</style></author><author><style face="normal" font="default" size="100%">Anton Bahtiar</style></author><author><style face="normal" font="default" size="100%">Vincent Kharisma Wangsaputra</style></author><author><style face="normal" font="default" size="100%">Norma Nur Azizah</style></author><author><style face="normal" font="default" size="100%">Wilzar Fachri</style></author><author><style face="normal" font="default" size="100%">Lince Dameria Nadapdap</style></author><author><style face="normal" font="default" size="100%">Ajeng Megawati Fajrin</style></author><author><style face="normal" font="default" size="100%">Hiroki Tanimoto</style></author><author><style face="normal" font="default" size="100%">Kiyomi Kakiuchi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Composition and Evaluation of Marine Algal Sargassum polycystum for Antioxidant Activity and In Vitro Cytotoxicity on Hela Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">HeLa cells</style></keyword><keyword><style  face="normal" font="default" size="100%">phytochemisty</style></keyword><keyword><style  face="normal" font="default" size="100%">Sargassum polycystum</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February  2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">88-94</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;&lt;em&gt;Sargassum polycystum&lt;/em&gt; is one of marine algal which has a potent antioxidant anticancer activities. This research aims to investigate phytochemical composition, antioxidant activity and &lt;em&gt;in vitro &lt;/em&gt;cytotoxicity of marine algal &lt;em&gt;Sargassum polycystum &lt;/em&gt;on cervical HeLa cancer.&lt;strong&gt; Methods:&lt;/strong&gt; &lt;em&gt;Sargassum polycystum&lt;/em&gt; collected from Dompu beach, Lombok, Nusa Tenggara Barat Province, Indonesia, were extracted into organic solvent of n-hexane, ethylacetate, chloroform and ethanol, respectively. Subsequently, &lt;em&gt;Sargassum polycystum&lt;/em&gt; extracts were applied for Thin Layer Chromatography (TLC) analysis, phytochemistry test, total phenolic and total flavonoid contents, as well as for antioxidant activity test by DPPH (2,2-diphenyl-1-picrylhydrazyl) method, and in vitro cytotoxicity evaluation on HeLa cells by MTT (3-[4,5-dimethylthiazol-2-yl]-2,5- diphenyltetrazolium bromide) assay. &lt;strong&gt;Results: &lt;/strong&gt;Phytochemical analysis of&lt;em&gt; S. polycystum&lt;/em&gt; extracts are positive for metabolites of flavonoid, steroid, tannin and glycoside. TLC analysis revealed that &lt;em&gt;S. polycystum&lt;/em&gt; extracts containing four phytochemical components. Ethylacetate extract of&lt;em&gt; S. polycystum&lt;/em&gt; showed the highest total phenolic content, and exhibited greater antioxidant activity than ethanol extract. Total phenolic and total flavonoid content in ethylacetate extract are 548.61 μg/mL and 40.06 μg /mL, respectively. Ethylacetate extract of &lt;em&gt;S. polycystum&lt;/em&gt; with IC&lt;sub&gt;50&lt;/sub&gt; value of 298.3 μg/mL is assigned to have a weak antioxidant activity against DPPH free radical. The results indicate that antioxidant activity of ethylacetate extracts of &lt;em&gt;S. polycystum&lt;/em&gt; is directly correlated with its total phenolic and flavonoid content. Moreover, &lt;em&gt;S. polycystum&lt;/em&gt; extracts demonstrated a strong anticancer activity on cervical HeLa cells with IC&lt;sub&gt;50 &lt;/sub&gt;ranging from 38.3 μg/mL to 112.8 μg/mL. &lt;strong&gt;Conclusion:&lt;/strong&gt; This work confirmed that S.polycystum are promising natural antioxidant and anti-cervical cancer agents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">88</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ade Arsianti&lt;sup&gt;1,2,&lt;/sup&gt;*, Anton Bahtiar&lt;sup&gt;3&lt;/sup&gt;, Vincent Kharisma Wangsaputra&lt;sup&gt;4&lt;/sup&gt;, Norma Nur Azizah&lt;sup&gt;2&lt;/sup&gt;, Wilzar Fachri&lt;sup&gt;5,2&lt;/sup&gt;, Lince Dameria Nadapdap&lt;sup&gt;2&lt;/sup&gt;, Ajeng Megawati Fajrin1, Hiroki Tanimoto&lt;sup&gt;6&lt;/sup&gt;, Kiyomi Kakiuchi&lt;sup&gt;6&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Medical Chemistry, Faculty of Medicine, University of Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Drug Development Research Cluster, Indonesia Medical Education and Research Institute (IMERI), Faculty of Medicine, University of Indonesia, Jalan Salemba Raya 6 Jakarta 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacology, Faculty of Pharmacy, University of Indonesia, Depok, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Medical Student, Faculty of Medicine University of Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Medical Pharmacy, Faculty of Medicine, University of Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma, Nara, JAPAN.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kanoktip Pansuksan</style></author><author><style face="normal" font="default" size="100%">Sophida Sukprasert</style></author><author><style face="normal" font="default" size="100%">Netiya Karaket</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Compounds in Arundo donax L. Rhizome and Antimicrobial Activities</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Bacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS</style></keyword><keyword><style  face="normal" font="default" size="100%">Giant reed</style></keyword><keyword><style  face="normal" font="default" size="100%">HCA</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">287-292</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;The aerial part of &lt;em&gt;Arundo donax&lt;/em&gt; L., giant reed, is a well-known fuel source used in many countries. &lt;strong&gt;Methods:&lt;/strong&gt; Phytochemical compounds in &lt;em&gt;A. donax&lt;/em&gt; L. rhizome, sequentially extracted with hexane (HEX), dichloromethane (DCM), ethyl acetate (EA), and methanol (MeOH), were identified using gas chromatography-mass spectrometry. Antimicrobial activities of the rhizome extracts were evaluated using disc diffusion assay against yeast (&lt;em&gt;Candida albicans&lt;/em&gt;), and bacteria Gram-positive (&lt;em&gt;Staphylococcus aureus &lt;/em&gt;ATCC 25923, &lt;em&gt;Bacillus cereus&lt;/em&gt; ATCC11778, and &lt;em&gt;Bacillus subtilis &lt;/em&gt;ATCC6633) and Gram-negative (&lt;em&gt;Escherichia coli&lt;/em&gt; ATCC25922). &lt;strong&gt;Results: &lt;/strong&gt;The detected phytochemicals were screened against WILEY07 library; 84 compounds matched with a similarity ≥ 90%. All the characterized compounds were grouped based on their functional group. The major phytochemicals in the HEX, DCM, and EA extracts belonged to sterol groups, while lipids, fatty acids, and related conjugates were the main components of the methanolic extract. The other characterized compounds were hydrocarbons, phenolics, terpenoids, xanthones, and xanthene. Growth of &lt;em&gt;B. subtilis&lt;/em&gt; was inhibited by the HEX, DCM, EA, and MeOH extracts, whereas B. cereus growth was inhibited only by the DCM and EA extracts. However, growth of &lt;em&gt;E. coli &lt;/em&gt;and &lt;em&gt;C. albicans&lt;/em&gt; could be not inhibited by &lt;em&gt;A. donax&lt;/em&gt; L. rhizome extracts. Analysis of the compounds as well as their antibacterial activities via hierarchical clustering showed that hexadecanoic acid is the major compound influencing &lt;em&gt;B. subtilis&lt;/em&gt; growth, while, B. cereus growth was affected by xanthone. &lt;strong&gt;Conclusions: &lt;/strong&gt;Rhizomes of &lt;em&gt;A. donax&lt;/em&gt; L. is one potential source of antimicrobial agents and further applied in medicinal uses.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">287</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kanoktip Pansuksan&lt;sup&gt;1,&lt;/sup&gt;*, Sophida Sukprasert&lt;sup&gt;1,2&lt;/sup&gt;, Netiya Karaket&lt;sup&gt;3,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Chulabhorn International College of Medicine, Thammasat University, 99, Phaholyothin Rd., Khlong 1 Sub District, Khlong Luang District, Pathumthani 12120, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Protein and Proteomics Research Center for Commercial and Industrial Purposes (ProCCI), Khonkaen University, Khonkaen, 40002, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;School of Interdisciplinary Studies, Mahidol University Kanchanaburi Campus, 199 Sangchuto Rd., Saiyok, Kanchanaburi, 71150, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ade Arsianti</style></author><author><style face="normal" font="default" size="100%">Gerry Kurniawan</style></author><author><style face="normal" font="default" size="100%">Nadzila Anindya Tejaputri</style></author><author><style face="normal" font="default" size="100%">Fona Qorina</style></author><author><style face="normal" font="default" size="100%">Qotrunnada Fithrotunnisa</style></author><author><style face="normal" font="default" size="100%">Norma Nur Azizah</style></author><author><style face="normal" font="default" size="100%">Ajeng Megawati Fajrin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Profile, Antioxidant Activity and Cell Line Study of Marine Red Macroalgae Eucheuma cottonii on Lung A-549 Cancer Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Cell line study</style></keyword><keyword><style  face="normal" font="default" size="100%">Eucheuma cottonii</style></keyword><keyword><style  face="normal" font="default" size="100%">Lung A-549 cells</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">276-281</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;In this century, cancer has increased in incidence and become one of the deadliest disease in the world. However, to date, lung cancer treatments are still not fully effective, quite expensive and very exhaustive for the patient. &lt;em&gt;Eucheuma cottonii&lt;/em&gt; is an abundant marine red macroalgae in Indonesia which have a potential anti-lung cancer properties. Aim of this research is to determine phytochemical profile of &lt;em&gt;Eucheuma cottonii &lt;/em&gt;extracts, as well as to evaluate its antioxidant and cytotoxic effects on Lung A-549 cancer cells.&lt;strong&gt; Methods:&lt;/strong&gt; &lt;em&gt;Eucheuma cottonii&lt;/em&gt; obtained from Sorong beach, West Papua Province, Indonesia, were extracted with three different solvents, that is ethanol, ethylacetate, and n-hexane. These three &lt;em&gt;Eucheuma cottonii &lt;/em&gt;extracts were identified for its phytochemical profiles, antioxidant activity by DPPH (2,2-diphenyl-1-picrylhydrazyl) assay, and cytotoxic activity on lung A-549 cells by MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) assay. &lt;strong&gt;Results:&lt;/strong&gt; Phytochemical analysis revealed that &lt;em&gt;Eucheuma cottonii&lt;/em&gt; contains metabolites of triterpenoid and alkaloid. Antioxidant activity evaluation showed ethanol extract of &lt;em&gt;Eucheuma cottonii &lt;/em&gt;has IC&lt;sub&gt;50&lt;/sub&gt; value of 559.76 μg/mL against DPPH free radical. Whereas cytotoxicity evaluation showed that ethanol extract and ethylacetate extract of &lt;em&gt;Eucheuma cottonii&lt;/em&gt; have cytotoxic effects on Lung A-549 cancer cells, with IC&lt;sub&gt;50 &lt;/sub&gt;value of 251.73 μg/ mL and 261.41 μg/mL, respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; These results suggesting that &lt;em&gt;Eucheuma cottonii &lt;/em&gt;extract could be further developed as a natural anti-lung cancer agent.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">276</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ade Arsianti&lt;sup&gt;1,2,&lt;/sup&gt;*, Gerry Kurniawan&lt;sup&gt;3&lt;/sup&gt;, Nadzila Anindya Tejaputri&lt;sup&gt;3&lt;/sup&gt;, Fona Qorina&lt;sup&gt;3&lt;/sup&gt;, Qotrunnada Fithrotunnisa&lt;sup&gt;3&lt;/sup&gt;, Norma Nur Azizah&lt;sup&gt;2&lt;/sup&gt;, Ajeng Megawati Fajrin&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Medical Chemistry, Faculty of Medicine, University of Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Drug Development Research Cluster, Indonesia Medical Education and Research Institute (IMERI), Faculty of Medicine, University of Indonesia, Jalan Salemba Raya 6 Jakarta 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Medical Student, Faculty of Medicine University of Indonesia, Jakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Awa KA</style></author><author><style face="normal" font="default" size="100%">Kady Diatta Badji</style></author><author><style face="normal" font="default" size="100%">Moustapha Bassimbé Sagna</style></author><author><style face="normal" font="default" size="100%">Aliou Guissé</style></author><author><style face="normal" font="default" size="100%">Emmanuel Bassène</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Screening and Antioxidant Activity of the Fruits of Boscia senegalensis (Pers.) Lam. e.g. Pear. (Capparaceae)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Boscia senegalensis</style></keyword><keyword><style  face="normal" font="default" size="100%">Fruits</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical screening</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1042-1049</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective: &lt;/strong&gt;This study aims to assess the phytochemical composition and antioxidant activity of the fruits (pulp and seeds) of &lt;em&gt;Boscia senegalensis&lt;/em&gt; from the Ferlo zone in Northern Senegal.&lt;strong&gt; Material and Methods: &lt;/strong&gt;Fruit collection of &lt;em&gt;Boscia senegalensis&lt;/em&gt; was carried out in three Ferlo’s localities: Tessékéré, Labgar and Ranérou. The sample consists of 36 individuals selected randomly from each locality. The major chemical groups were determined by conventional methods using specific general reagents. The determination of total polyphenols and total flavonoids, the 2,2-diphenyl-1picrylhydrazyl (DPPH.) radical scavenging activity and ferric reducing of antioxidant power (FRAP) were evaluated by spectrophotometry. &lt;strong&gt;Results and Discussion: &lt;/strong&gt;The results of the photochemical screening revealed the presence of saponins, alkaloids, sterols and triterpenes, flavonoids and polyphenols in both parts of the fruit (pulp and seeds). Assays carried out on extracts of pulp and seed powders reveals higher levels of total polyphenols and flavonoids in the pulp. The study of antioxidant activity has shown that hydro-ethanol extracts of pulp and seeds have a very interesting reducing activity, particularly in the pulp. However, we can see a weak antiradical activity of these extracts. The origin effect has a weak influence on the antiradical and reducing activity of the pulp and seed extracts.&lt;strong&gt; Conclusions: &lt;/strong&gt;The biological activity of the harvested &lt;em&gt;Boscia senegalensis&lt;/em&gt; extracts highlighted in this study could justify the traditional uses of this plant in the treatment of several pathologies. This fruit should be consumed in order to prevent few dietary imbalances or valorized in order to develop new bioactive compounds.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1042</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Awa KA&lt;sup&gt;1,2&lt;/sup&gt;, Kady Diatta Badji&lt;sup&gt;1,4&lt;/sup&gt;, Moustapha Bassimbé Sagna&lt;sup&gt;2&lt;/sup&gt;, Aliou Guissé&lt;sup&gt;2,3,4,&lt;/sup&gt;*, Emmanuel Bassène&lt;sup&gt;1,4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Pharmacognosy and Botany Laboratory, Cheikh Anta Diop University, B.P. 5005, Dakar-Fann, SÉNÉGAL.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Plant Biology, Faculty of Science and Technology, Cheikh Anta Diop University, B.P.5005. Dakar-Fann, SÉNÉGAL.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Human Observatory International Environment, Tessékéré (UCAD/CNRS), SÉNÉGAL.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;UMI 3189 &quot;Environment, Health, Societies&quot;, SÉNÉGAL.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Apinya Rachkeeree</style></author><author><style face="normal" font="default" size="100%">Kuttiga Kantadoung</style></author><author><style face="normal" font="default" size="100%">Ratchadawan Puangpradub</style></author><author><style face="normal" font="default" size="100%">Ratchuporn Suksathan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemicals, Antioxidants and Anti-tyrosinase Analyses of Selected Ginger Plants</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ABTS assay</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-tyrosinase</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH assay</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolic content</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword><keyword><style  face="normal" font="default" size="100%">Zingiberaceae</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">872-883</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Some of Zingeberaceae are not widely used for medicine of food, although in Thailand have been used them for many reasons about health or the diet. This study evalued the phytochemicals and anti-tyrosinase activities of 16 plant species of &lt;em&gt;Alpinia, Amomum, Curcuma, Etlingera&lt;/em&gt; and &lt;em&gt;Kaemferia &lt;/em&gt;(Zingiberaceae). &lt;strong&gt;Methods:&lt;/strong&gt; The extractions of dried powdered rhizomes were performed using n-hexane, ethylacetate and ethanol. Percentage extract yield of the samples varied among species and solvent extracts. Chemical groups (alkaloids, flavonoids, tannins, polyphenols, steroids and terpenoids) were identified using phytochemical screening. The total phenolic contents (TPC) were analyzed using the Folin-Ciocalteu’s reagent, while antioxidant activities were detected using 2,2-diphenyl-1- picrylhydrazyl (DPPH) and the 2,2’-azino-bis (3-ethylbenzothizoline-6-sulphonic acid) (ABTS.+). The anti-tyrosinase was expressed to the half maximal inhibitory concentration (IC&lt;sub&gt;50&lt;/sub&gt;) value (mg/mL). &lt;strong&gt;Results:&lt;/strong&gt; The ethyl acetate extract of &lt;em&gt;Amomum &lt;/em&gt;showed the highest value of TPC. The strongest antioxidant activity were found in &lt;em&gt;Amomum&lt;/em&gt; and &lt;em&gt;Kaemferia&lt;/em&gt; extracts, while ethyl acetate and ethanol extracts of all samples have a better antioxidant properties than the n-hexane extracts. On the other hand, the n-hexane extracts have the highest anti-tyrosinase potential in all samples and of these, &lt;em&gt;Curcuma&lt;/em&gt; extracts were the best group. &lt;strong&gt;Conclusion: &lt;/strong&gt;Our research indicated that plants of the Zingiberaceae would be new sources of antioxidants and anti-tyrosinase for further natural product developments in cosmetics, food or nutraceuticals.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">872</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Apinya Rachkeeree, Kuttiga Kantadoung, Ratchadawan Puangpradub, Ratchuporn Suksathan*&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Queen Sirikit Botanic Garden, The Botanical Garden Organization, P.O. Box 7 Mae Rim, Chiang Mai, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rungtiwa Kanthain</style></author><author><style face="normal" font="default" size="100%">Supawatchara Singhatong</style></author><author><style face="normal" font="default" size="100%">Surapol Natakankitkul</style></author><author><style face="normal" font="default" size="100%">Nathupakorn Dechsupa</style></author><author><style face="normal" font="default" size="100%">Jirakrit Leelarungrayub</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Potential of Hard Candy Containing Spray-Dried Vernonia cinerea Extract with Total Phenolic Compounds, Total Flavonoids and Nicotine Replacement as an Anti-Smoking Aid</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Hard candy</style></keyword><keyword><style  face="normal" font="default" size="100%">Nicotine</style></keyword><keyword><style  face="normal" font="default" size="100%">Total flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Total phenolic compounds</style></keyword><keyword><style  face="normal" font="default" size="100%">Vernonia cinerea</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February  2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">35-43</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Backgound: &lt;/strong&gt;&lt;em&gt;Vernonia cinerea&lt;/em&gt; (VC) is a natural plant claimed to reduce cigarette smoking. Some pilot anti-smoking products with nicotine replacement, such as lozenges or gum, have been presented, but with some adverse effects. Thus, application of VC as a new-anti-smoking product is very challenging. &lt;strong&gt;Objectives: &lt;/strong&gt;The aims of this study were to compare the active compounds; total phenolic compounds, total flavonoids and nicotine, and study antioxidant activity on scavenging 2,2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) and 1,1-diphenyl-2-picryl hydrzayl (DPPH) radicals of extracts prepared by spray drying (SD) and freeze drying (FD) techniques for pilot hard candy. &lt;strong&gt;Methods: &lt;/strong&gt;Raw VC materials of mixed parts, i.e., the stem, flowers and leaves, were made to form extracts by FD and SD techniques. Then, extract from the SD technique was manufactured industrially into hard candy containing glucose syrup and refined glucose. Total phenolic compounds, total flavonoids, nicotine, scavenging activity of extracts, VC hard candy and placebo candy were evaluated by folin-ciocalteau reagent, aluminum chloride colorimetric assay, high-performance liquid chromatography, ABTS cation decolorization and DPPH protocols.&lt;strong&gt; Results: &lt;/strong&gt;Total phenolic compounds were significantly different between extracts, but total flavonoids and nicotine were slightly higher in SD extract. Antioxidant activity of both extracts on ABTS radicals was not significantly different, but the half-maximal inhibitory concentration (IC&lt;sub&gt;50&lt;/sub&gt;) on DPPH radicals was significantly higher in SD extract when compared to the FD extract. Finally, total phenolic compounds, total flavonoids and nicotine, as well as scavenging activity could be detected in hard candy. &lt;strong&gt;Conclusion: &lt;/strong&gt;VC can be used as an anti-smoking aid with nicotine replacement and anti-oxidant compounds in pilot hard candy.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">35</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Rungtiwa Kanthain&lt;sup&gt;1&lt;/sup&gt;, Supawatchara Singhatong&lt;sup&gt;2&lt;/sup&gt;, Surapol Natakankitkul&lt;sup&gt;3&lt;/sup&gt;, Nathupakorn Dechsupa&lt;sup&gt;4&lt;/sup&gt;, Jirakrit Leelarungrayub&lt;sup&gt;5,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Movement and Exercise Sciences, Department of Physical Therapy, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Division of Clinical Chemistry, Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmaceutical Sciences, Faculty of Pharmacy, Chiang Mai University, Chiang Mai 50200, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Radiologic Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Physical Therapy, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sakulrat Rattanakiat</style></author><author><style face="normal" font="default" size="100%">Pawitra Pulbutr</style></author><author><style face="normal" font="default" size="100%">Wanwisa Khunawattanakul</style></author><author><style face="normal" font="default" size="100%">Bunleu Sungthong</style></author><author><style face="normal" font="default" size="100%">Kritsanee Saramunee</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Prebiotic Activity of Polysaccharides Extracted from Jerusalem Artichoke Tuber and Development of Prebiotic Granules</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Granule</style></keyword><keyword><style  face="normal" font="default" size="100%">Helianthus tuberosus</style></keyword><keyword><style  face="normal" font="default" size="100%">Jerusalem artichoke</style></keyword><keyword><style  face="normal" font="default" size="100%">Prebiotic effect</style></keyword><keyword><style  face="normal" font="default" size="100%">Probiotics</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Research Article</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1402-1411</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Jerusalem artichoke tubers (JA) contain non-digestible carbohydrates, especially inulin-type fructans, which have been found to possess various benefits on human health, including the prebiotic effect. Although many studies established the prebiotic property of inulin or fructo-oligosaccharides, there are less information of the prebiotic potential of JA crude extract. This study aimed to investigate prebiotic effect of the JA extract and develop prebiotic granules from JA extract.&lt;strong&gt; Material and Methods: &lt;/strong&gt;Crude polysaccharide extract of JA was obtained using hot water and freeze-dried method. The selected probiotics, including&lt;em&gt; L. plantarum, L. acidophilus, B. longum&lt;/em&gt; and&lt;em&gt; B. breve &lt;/em&gt;were used in this study. The prebiotic effect of the JA extract was indicated by bacterial growth and acid production. Parallelly, JA extract granule formulation was developed to be a prebiotic food product. &lt;strong&gt;Results:&lt;/strong&gt; The JA extract at the highest concentration tested (2%) caused a significant increase in the growth and acid production of every probiotics tested, including&lt;em&gt; L. plantarum, L. acidophilus, B. longum &lt;/em&gt;and &lt;em&gt;B. breve.&lt;/em&gt; The growth promoting effects of the 2% JA extract were detected as early as 12 hour-incubation, and this action was maintained throughout the observed incubation period.&lt;strong&gt; Conclusions:&lt;/strong&gt; The developed JA extract granules possessed desirable properties with the moisture content of 4.00±0.20%. The formulated granule was soluble in water and produced a brown and clear solution with slightly sweet taste. Nonetheless,&lt;em&gt; in vivo&lt;/em&gt; experiments on the prebiotic effect of the developed preparation should be performed further.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1402</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sakulrat Rattanakiat&lt;sup&gt;1,&lt;/sup&gt;*, Pawitra Pulbutr&lt;sup&gt;1&lt;/sup&gt;, Wanwisa Khunawattanakul&lt;sup&gt;1&lt;/sup&gt;, Bunleu Sungthong&lt;sup&gt;1&lt;/sup&gt;, Kritsanee Saramunee&lt;sup&gt;1 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Pharmacy, Mahasarakham University, Maha Sarakham, 44150, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dwirini Retno Gunarti</style></author><author><style face="normal" font="default" size="100%">Megawati Kartika</style></author><author><style face="normal" font="default" size="100%">Mohamad Sadikin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Properties of A Thiamine Binding Protein Purified from Mung Bean</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Binding capacity</style></keyword><keyword><style  face="normal" font="default" size="100%">Mung bean thiamine binding protein (MBTBP)</style></keyword><keyword><style  face="normal" font="default" size="100%">Thiamine</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">266-270</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Thiamine (vitamin B1) was the first B vitamin which has been identified. It serves as a cofactor for several enzymes involved in energy metabolism. The laboratory test against thiamine deficiency can be done by measuring thiamine levels in the blood. The aim of this study was to identify the stability and the binding activity characters of TBP. The equilibrium dialysis technique was used to see the factors affecting the bond between TBP and thiamine. The MBTBP concentration of post-chromatographic affinity resulted from dilution of lyophilisate was stable for 30 days at -20°C and 3 days at 4°C. The optimal pH for binding MBTBP to thiamine was 7.5. Alkylation with iodoacetic acid decreased the binding capacity of TBP which suggested the presence of a–SH or imidazol group in its active site. The importance of disulfide bridge was proven by decreasing of Thiamine binding capacity of TBP after β-mercaptoethanol treatment. This binding activity was also affected by oxidizing agents, but it was less affected by calcium ions and heavy metals.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">266</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Dwirini Retno Gunarti&lt;sup&gt;1,&lt;/sup&gt;*, Megawati Kartika&lt;sup&gt;2&lt;/sup&gt;, Mohamad Sadikin&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Departement Biochemistry and Molecular Biology, Faculty of Medicine, University of Indonesia, Jl. Salemba Raya No. 6, Jakarta 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Master Program in Biomedical Science, Faculty of Medicine, University of Indonesia, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sergey Kondrashev</style></author><author><style face="normal" font="default" size="100%">Nadezhda Nesterova</style></author><author><style face="normal" font="default" size="100%">Alexey Luzin</style></author><author><style face="normal" font="default" size="100%">Vitaliy Kochanov</style></author><author><style face="normal" font="default" size="100%">Anna Luzina</style></author><author><style face="normal" font="default" size="100%">Alexey Matyushin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Qualitative and Quantitative Assay of Hydroxycinnamates of Prunus spinosa L.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Blackthorn</style></keyword><keyword><style  face="normal" font="default" size="100%">Herbal raw material</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydroxycinnamic acids</style></keyword><keyword><style  face="normal" font="default" size="100%">Prunus Spinosa L.</style></keyword><keyword><style  face="normal" font="default" size="100%">Spectrophotometry</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February  2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">157-161</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Blackthorn (&lt;em&gt;Prunus spinosa &lt;/em&gt;L.) is a plant commonly found in the Russian Federation on the roadsides, forest margins, and meadows. Despite lack of recognition by the official medicine, blackthorn fruits possess antioxidant properties and are used in homeopathic preparations. They may also demonstrate antibacterial and anticancer potential due to hydroxycinnamic acids. The aim of present study was to identify and assay hydroxycinnamates in fruits of &lt;em&gt;P. spinosa&lt;/em&gt; cultivated in Moscow Region. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Fresh and dried fruits of &lt;em&gt;P. spinosa&lt;/em&gt;, gathered from plants cultivated in Moscow Region in the harvest maturity stage, were used in the study. Qualitative composition of hydroxycinnamic acids was assessed by high performance liquid chromatography, using reversed phase C18 column. Total hydroxycinnamic acids (THA) content was assessed spectrophotometrically.&lt;strong&gt; Results:&lt;/strong&gt; Similar chromatographic profiles were obtained for both fresh and dried blackthorn fruits, the two most abundant compounds being epicatechin (2.91%) and chicoric acid (2.90%). Fruits gathered in Chekhovsky District had lower content of hydroxycinnamates (0.798 ± 0.89) than those coming from Klinsky District (0.886 ± 0.92). However, the THA content in dried fruits grown in both districts was found to be similar (0.540 ± 0.71 and 0.557 ± 0.74, respectively).&lt;strong&gt; Conclusions: &lt;/strong&gt;It can be concluded that blackthorn fruits can be considered as a source of hydroxycinnamic acids, as both fresh and dried fruits contain at least eleven hydroxycinnamates. It was found that the dried fruits have similar content of hydroxycinnamic acids, independently of their origin. Future research should be aimed at drying method optimization.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">157</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Sergey Kondrashev&lt;sup&gt;1&lt;/sup&gt;, Nadezhda Nesterova&lt;sup&gt;3&lt;/sup&gt;, Alexey Luzin&lt;sup&gt;1&lt;/sup&gt;, Vitaliy Kochanov&lt;sup&gt;1&lt;/sup&gt;, Anna Luzina&lt;sup&gt;4&lt;/sup&gt;, Alexey Matyushin&lt;sup&gt;2,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry, Sechenov First Moscow State Medical University, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Analytical and Forensic Toxicology, Sechenov First Moscow State Medical University, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Natural Science in Pharmacy, Sechenov First Moscow State Medical University, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Dentistry, Sechenov First Moscow State Medical University, Moscow, RUSSIAN FEDERATION.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jagadeep Chandra S</style></author><author><style face="normal" font="default" size="100%">Chandana GL</style></author><author><style face="normal" font="default" size="100%">Naganagouda V Kote</style></author><author><style face="normal" font="default" size="100%">Sharath Chandra SP</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Recent Scenario of Impact of Xenobiotics on Marine Fish: An Overview</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Fish</style></keyword><keyword><style  face="normal" font="default" size="100%">Litters</style></keyword><keyword><style  face="normal" font="default" size="100%">Marine</style></keyword><keyword><style  face="normal" font="default" size="100%">Xenobiotics</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1797-1800</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Xenobiotics from chemicals to plastics have seriously interfered with the biological process of living system. Their impact on aquatic ecosystem, fish in precise is studied with significant interest. However, studies on impact of xenobiotics on marine fish are limited. This literature review integrates and summarizes the impact of xenobiotics on marine fish. The review tries to understand the impact of macro and micro litters, microplastic, metals like mercury and nanoparticles. Finally, we conclude with the ways to regulate the presence and distribution of these xenobiotics in marine environment.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">1797</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Jagadeep Chandra S&lt;sup&gt;1&lt;/sup&gt;, Chandana GL&lt;sup&gt;2&lt;/sup&gt;, Naganagouda V Kote&lt;sup&gt;3&lt;/sup&gt;, Sharath Chandra SP&lt;sup&gt;4,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Microbiology, Faculty of Life Sciences, JSS Academy of higher education and research, Mysuru, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biochemistry, Hassan Institute of Medical Sciences, Hassan, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biochemistry, Maharani`s Science College for Women, Bengaluru, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biochemistry, Government Science College, Hassan, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nandhini S</style></author><author><style face="normal" font="default" size="100%">Ilango K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Simultaneous Quantification of Lupeol, Stigmasterol and β- Sitosterol in Extracts of Adhatoda vasica Nees Leaves and its Marketed Formulations by a Validated RP-HPLC Method</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adhatoda vasica Nees</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Lupeol</style></keyword><keyword><style  face="normal" font="default" size="100%">Simultaneous quantification</style></keyword><keyword><style  face="normal" font="default" size="100%">Stigmasterol</style></keyword><keyword><style  face="normal" font="default" size="100%">β-sitosterol</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">850-856</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Adhatoda vasica &lt;/em&gt;Nees (Acanthaceae) is a well-known medicinal plant used for the treatment of respiratory disorders such as asthma and bronchitis. &lt;strong&gt;Objective: &lt;/strong&gt;To develop a simple and precise RP-HPLC method for the simultaneous assessment of lupeol, stigmasterol and β-sitosterol of various extracts of &lt;em&gt;Adhatoda vasica &lt;/em&gt;Nees. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;The compounds were separated on RP-Phenomenex C&lt;sub&gt;18 &lt;/sub&gt;(250mm×4.6mm; 5μ) column with a mobile phase comprising of 0.1%v/v formic acid in water and methanol (28:82%v/v) splashed at a flow of 0.8mL/min with PDA detector at 208nm. &lt;strong&gt;Results: &lt;/strong&gt;The retention time of lupeol, stigmasterol and β-sitosterol was found to be 16.89, 18.26 and 20.72 minutes respectively. The amount of lupeol was abundant in hexane extract (0.952%w/w) and formulation III (23.72ng/g) whereas, stigmasterol (0.285%w/w) and β-sitosterol (8.649%w/w) was highly abundant in chloroform extract and formulation I stigmasterol (2.57ng/g) and β-sitosterol (0.98ng/g). The optimized method was validated for different parameters and all the validated constraints were within the limits as per ICH guidelines. The proposed method was linear over the concentration range of 12.5-200μg/mL with correlation coefficients greater than 0.997. The LOD and LOQ values of lupeol, stigmasterol and β-sitosterol were found to be 0.66, 5.64 and 12.8μg/mL and 2.01, 17.10 and 36.62μg/mL respectively. &lt;strong&gt;Conclusion: &lt;/strong&gt;To conclude, the developed method for the simultaneous estimation of lupeol, stigmasterol and β-sitosterol was simple, precise, accurate and thus reliable for the quality control investigations of crude drugs and its herbal formulations.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">850</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nandhini S&lt;sup&gt;1&lt;/sup&gt;, Ilango K&lt;sup&gt;1,2,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Pharmacognosy and Phytochemistry, Interdisciplinary Institute of Indian System of Medicine (IIISM), SRM Institute of Science and Technology, Kattankulathur - 603 203, Chengalpattu (Dt), Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Chemistry, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur- 603 203, Chengalpattu (Dt), Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Angelina V Strelyaeva</style></author><author><style face="normal" font="default" size="100%">Olga A Larina</style></author><author><style face="normal" font="default" size="100%">Alla M Antsyshkina</style></author><author><style face="normal" font="default" size="100%">Roman M Kuznetsov</style></author><author><style face="normal" font="default" size="100%">Alina A Bondar</style></author><author><style face="normal" font="default" size="100%">Vladimir A Sorokin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Study of External Signs, Microscopy and Chemical Composition of Medicinal Plant Materials of Verоnica beccabunga L. Herb</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">1-Benzyl-1H-benzimidazole 3-oxide</style></keyword><keyword><style  face="normal" font="default" size="100%">Verоnica beccabunga L.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">391-403</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Veronica beccabunga&lt;/em&gt; L. belongs to the class dicotyledons, order &lt;em&gt;Lamiáles&lt;/em&gt;, family &lt;em&gt;Scrophulariaceae.&lt;/em&gt; Representatives of the genus Veronica have long been used in folk medicine as antiinflammatory, antibacterial, antiseptic, wound healing, hemostatic, choleretic and antispasmodic drugs. Widely studied species are &lt;em&gt;Veronica officinalis&lt;/em&gt; and&lt;em&gt; Veronica chamaedrys.&lt;/em&gt; &lt;em&gt;Veronica beccabunga &lt;/em&gt;L., which is the object of our study, remains a poorly studied plant. &lt;strong&gt;Aim:&lt;/strong&gt; The study of external signs, microscopy and chemical composition of medicinal plant materials of &lt;em&gt;Verоnica beccabunga&lt;/em&gt; L. herb. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Chromato-mass spectrometry was used in the work. &lt;strong&gt;Results and Discussion: &lt;/strong&gt;When describing external signs and microscopy, diagnostic signs of &lt;em&gt;Verоnica beccabunga&lt;/em&gt; were revealed. 27 compounds were identified by chromatography-mass spectrometry. The maximum content falls on: Citronellol epoxide (R or S) (30.5 %), Linolenic acid, ethyl ester (15.18), Diethyl succinate (12.17%), Ethyl palmitate (6.43%), Phytol (4.89%), Acetaldehyde ethyl amyl acetal (3.94%), Dibenzylamine (3.01%), Oleamide (2.77%), 2-(1-Methylbutyl)oxirane (2.7%), Butyl octyl phthalate(1.7%), Ethyl 10-bromodecanoate (1.68), Valeric acid, 4-methyl-, ethyl ester (1.58). Glycoside detected : 1-Benzyl-1Hbenzimidazole 3-oxide (0.76%). &lt;strong&gt;Conclusion: &lt;/strong&gt;The revealed morphological and anatomical signs of &lt;em&gt;Verоnica beccabunga &lt;/em&gt;herb can be used to diagnose this species and develop authenticity indicators for promising medicinal herbs. 27 compounds were identified by chromatographymass spectrometry. Using the method of simple normalization, the relative percentage of identified compounds was determined.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">391</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Angelina V Strelyaeva, Olga A Larina*, Alla M Antsyshkina, Roman M Kuznetsov, Alina A Bondar, Vladimir A Sorokin &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;I.M. Sechenov First Moscow State Medical University, Pharmaceutical Natural, Science Department Izmailovsky Boulevard, 8, 105043, Moscow, RUSSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Emelia Oppong Bekoe</style></author><author><style face="normal" font="default" size="100%">Cindy Kitcher</style></author><author><style face="normal" font="default" size="100%">Philip Debrah</style></author><author><style face="normal" font="default" size="100%">Patrick Amoateng</style></author><author><style face="normal" font="default" size="100%">Paul Owusu Donkor</style></author><author><style face="normal" font="default" size="100%">Sarfoa Martinson</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Study on Phyllanthus amarus; Pharmacognostic, Mycobactericidal and Mutagenic Properties</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Fluorescence</style></keyword><keyword><style  face="normal" font="default" size="100%">Mutagenic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">P. amarus</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognostic</style></keyword><keyword><style  face="normal" font="default" size="100%">Tuberculosis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1732-1739</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Phyllanthus amarus&lt;/em&gt; is a medicinal plant used in the treatment of various ailments which include gonorrhoea, jaundice, diabetes, kidney diseases, bladder and intestinal infections, influenza, measles, viral infections, and tuberculosis. Tuberculosis treatment is faced with many challenges, resulting in a prolonged treatment regimen and potential treatment failure. There is a need to search for more favourable treatment options. &lt;strong&gt;Objective:&lt;/strong&gt; This study aimed at investigating the pharmacognostic and mycobactericidal properties of &lt;em&gt;P. amarus. &lt;/em&gt;Since toxicity could also be an issue, the mutagenic activity of this plant was also assessed. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The macroscopic, microscopic, and physicochemical characteristics were assessed with reference to the Quality Control Methods for Herbal Material WHO (2011). The mycobactericidal activity was determined by the agar diffusion and broth dilution methods, while mutagenicity was investigated by the Ames test. &lt;strong&gt;Results:&lt;/strong&gt; &lt;em&gt;P. amarus &lt;/em&gt;contained tannins, flavonoids, glycosides, saponins and steroids. The 50% ethanol extract exhibited activity against &lt;em&gt;M. smegmatis&lt;/em&gt; at 100 mg/mL with an inhibitory zone of 2.0 cm.&lt;em&gt; P. amarus&lt;/em&gt; had a minimum inhibitory concentration of 50 mg/mL while that of rifampin was 0.1 μg/mL. &lt;em&gt;P. amarus&lt;/em&gt; showed weak mutagenicity at a concentration of 10 μg/mL. &lt;strong&gt;Conclusion:&lt;/strong&gt; The documented pharmacognostic characteristics can be used for quality control of the crude plant material. The mycobactericidal activity also affirmed its folkloric use in the treatment of tuberculosis. The mycobactericidal activity can be further exploited for drug development.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1732</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Emelia Oppong Bekoe&lt;sup&gt;1,&lt;/sup&gt;*, Cindy Kitcher&lt;sup&gt;1&lt;/sup&gt;, Philip Debrah&lt;sup&gt;2&lt;/sup&gt;, Patrick Amoateng&lt;sup&gt;3&lt;/sup&gt;, Paul Owusu Donkor&lt;sup&gt;1&lt;/sup&gt;, Sarfoa Martinson&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy and Herbal Medicine, School of Pharmacy, University of Ghana, GHANA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutics and Microbiology, School of Pharmacy, University of Ghana, GHANA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacology and Toxicology, School of Pharmacy, University of Ghana, GHANA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ade Arsianti</style></author><author><style face="normal" font="default" size="100%">Anton Bahtiar</style></author><author><style face="normal" font="default" size="100%">Fadilah Fadilah</style></author><author><style face="normal" font="default" size="100%">Vincent Kharisma Wangsaputra</style></author><author><style face="normal" font="default" size="100%">Rafika Indah Paramita</style></author><author><style face="normal" font="default" size="100%">Norma Nur Azizah</style></author><author><style face="normal" font="default" size="100%">Lince Dameria Nadapdap</style></author><author><style face="normal" font="default" size="100%">Ajeng Megawati Fajrin</style></author><author><style face="normal" font="default" size="100%">Hiroki Tanimoto</style></author><author><style face="normal" font="default" size="100%">Kiyomi Kakiuchi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis, Characterization, and Cytotoxicity Evaluation of Gallic Acid Nanoparticles Towards Breast T47D Cancer Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Gallic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Nanoparticle</style></keyword><keyword><style  face="normal" font="default" size="100%">Synthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">T47D cells</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">321-327</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Gallic acid is a naturally polyphenolic acid which shows cytotoxicity against several cancer cells, as well as it displays chemo-preventive activity which is attributed to its strong apoptosis- inducing and antioxidant effects. Thus, gallic acid has become an attractive substance to be further developed due to its strong cytotoxic activity. This study aimed to synthesize gallic acid nanoparticle coating with alginate-chitosan, and evaluate its cytotoxicity against breast T47D cancer cells.&lt;strong&gt; Methods: &lt;/strong&gt;Gallic acid nanoparticle was synthesized using ionic gelation method. The yield, size and morphology of the nanoparticles were determined by UV-Vis Spectroscopy, Transmission electron microscopy (TEM) and Fourier Transform Infrared (FTIR) spectroscopy. Cytotoxicity evaluation of gallic acid nanoparticle towards breast T47D cancer cell is carried out by MTT(3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazoliumbromide) assay. &lt;strong&gt;Results:&lt;/strong&gt; Spherical nanoparticles of gallic acid with the size of 100-200 nm has been successfully synthesized in 96% of yield. Compared to gallic acid (IC&lt;sub&gt;50&lt;/sub&gt;: 20.86 μg/mL) and alginate-chitosan nanoparticle (IC&lt;sub&gt;50&lt;/sub&gt;: 38.46 μg/mL), gallic acid coating with alginate-chitosan nanoparticles demonstrated higher cytotoxicity towards breast T47D cancer cells with IC&lt;sub&gt;50 &lt;/sub&gt;value of 9.03μg/mL. &lt;strong&gt;Conclusion:&lt;/strong&gt; Our results clearly confirmed that gallic acid nanoparticles coating with alginate-chitosan showed a strong cytotoxicity towards breast T47D cancer cells, which is potential to be developed as a candidate for new anti-breast cancer agent.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">321</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Ade Arsianti&lt;sup&gt;1,2,&lt;/sup&gt;*, Anton Bahtiar&lt;sup&gt;3&lt;/sup&gt;, Fadilah Fadilah&lt;sup&gt;1,2&lt;/sup&gt;, Vincent Kharisma Wangsaputra&lt;sup&gt;4&lt;/sup&gt;, Rafika Indah Paramita&lt;sup&gt;1&lt;/sup&gt;, Norma Nur Azizah&lt;sup&gt;2&lt;/sup&gt;, Lince Dameria Nadapdap&lt;sup&gt;2&lt;/sup&gt;, Ajeng Megawati Fajrin&lt;sup&gt;1&lt;/sup&gt;, Hiroki Tanimoto&lt;sup&gt;5&lt;/sup&gt;, Kiyomi Kakiuchi&lt;sup&gt;5 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Medical Chemistry, Faculty of Medicine, University of Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Drug Development Research Cluster, Indonesia Medical Education and Research Institute (IMERI), Faculty of Medicine, University of Indonesia, Jalan Salemba Raya 6 Jakarta 10430, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacology, Faculty of Pharmacy, University of Indonesia, Depok, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Medical Student, Faculty of Medicine University of Indonesia, Jakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma, Nara, JAPAN.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kartini Kartini</style></author><author><style face="normal" font="default" size="100%">Ervina Rustiana Dewi</style></author><author><style face="normal" font="default" size="100%">Fandi Achmad</style></author><author><style face="normal" font="default" size="100%">Nikmatul Ikhrom Eka Jayani</style></author><author><style face="normal" font="default" size="100%">Mochammad Arbi Hadiyat</style></author><author><style face="normal" font="default" size="100%">Christina Avanti</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thin Layer Chromatography Fingerprinting and Clustering of Orthosiphon stamineus Benth. from Different Origins</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Geographical origin</style></keyword><keyword><style  face="normal" font="default" size="100%">Herbal medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Marker</style></keyword><keyword><style  face="normal" font="default" size="100%">Principal Component Analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Quality</style></keyword><keyword><style  face="normal" font="default" size="100%">TLC</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February  2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">79-87</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Orthosiphon stamineus&lt;/em&gt; has been widely used across Asian countries for the treatment of various diseases. The quality of herbal medicine determine its safety as well as efficacy; and geographical origin is important factor contributing on the quality of herb and its products. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Thin Layer Chromatography (TLC) method combined with chemometric, Principal Component Analysis (PCA), has been employed to evaluate the quality of &lt;em&gt;Orthosiphon stamineus&lt;/em&gt; leaves collected from eleven origins in Indonesia.&lt;strong&gt; Results:&lt;/strong&gt; The results showed that mobile phase suitable for &lt;em&gt;Orthosiphon stamineus&lt;/em&gt; was chloroform, dichloromethane, ethyl acetate (7:4:1). The method used has met the requirements of TLC system stability and precision. TLC-fingerprints analyzed with chemometrics showed an ability to discriminate &lt;em&gt;Orthosiphon stamineus&lt;/em&gt; from various origins. PCA score plot of the first two principal components (PC) clearly distinguished 3 clusters of samples, whereas the loading plot of the first two PC showed that compounds with the Rf values of 0.0-0.1, 0.1-0.2, 0.2-0.3, and 0.9-1.0 are the most important compounds for clustering of samples. &lt;strong&gt;Conclusions:&lt;/strong&gt; TLCfingerprint combined with the PCA was able to discriminate among the leaves of &lt;em&gt;Orthosiphon stamineus&lt;/em&gt; originated from various locations. TLC-fingerprints analyzed with chemometrics can be used as an alternative of marker-oriented method to evaluate the quality of &lt;em&gt;Orthosiphon stamineus.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">79</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kartini Kartini&lt;sup&gt;1,&lt;/sup&gt;*, Ervina Rustiana Dewi&lt;sup&gt;1&lt;/sup&gt;, Fandi Achmad&lt;sup&gt;1&lt;/sup&gt;, Nikmatul Ikhrom Eka Jayani&lt;sup&gt;1&lt;/sup&gt;, Mochammad Arbi Hadiyat&lt;sup&gt;2&lt;/sup&gt;, Christina Avanti&lt;sup&gt;3&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Biology, Faculty of Pharmacy, University of Surabaya, Raya Kalirungkut Road, Surabaya 60293, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Industrial Engineering, Faculty of Engineering, University of Surabaya, Raya Kalirungkut Road, Surabaya 60293, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmaceutic, Faculty of Pharmacy, University of Surabaya, Raya Kalirungkut Road, Surabaya 60293, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hesham I Elaskary</style></author><author><style face="normal" font="default" size="100%">Omar M Sabry</style></author><author><style face="normal" font="default" size="100%">Asmaa M Khalil</style></author><author><style face="normal" font="default" size="100%">Soheir M El Zalabani</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">UPLC-PDA-ESI-MS/MS Profiling of Clerodendrum inerme and Clerodendrum splendens and Significant Activity Against Mycobacterium tuberculosis</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Clerodendrum</style></keyword><keyword><style  face="normal" font="default" size="100%">Diterpenoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Iridoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Mycobacterium</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenyl-propanoids</style></keyword><keyword><style  face="normal" font="default" size="100%">UPLC profiling</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2020</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">1518-1524</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Antibiotic resistance is a major problem that is spreading and increasing while the development of new antibiotics is ceasing. As a result, some bacterial infections that were easily treated previously became untreatable. The antibacterial activity of &lt;em&gt;Clerodendrum inerme&lt;/em&gt; and &lt;em&gt;Clerodendrum splendens &lt;/em&gt;leaves were investigated against Mycobacterium tuberculosis, the widely known multi-drug resistant bacterium. UPLC-PDA-ESI-MS/MS is characterized by high sensitivity, resolution and speed for identification of plant metabolites even the minor ones. The chemical constituents of the leaves of &lt;em&gt;C. inerme &lt;/em&gt;and&lt;em&gt; C. splendens&lt;/em&gt; were investigated by UPLC-PDA-ESI-MS/MS metabolic analysis. &lt;strong&gt;Methods: &lt;/strong&gt;The antibacterial activity of the ethanol extracts of the leaves of the two species under investigation was evaluated against the multi-ethanol drug resistant bacterium &lt;strong&gt;Mycobacterium tuberculosis&lt;/strong&gt; using MABA assay. The methanol extracts of the leaves of &lt;em&gt;C. inerme&lt;/em&gt; and &lt;em&gt;C. splendens&lt;/em&gt; were subjected to comparative UPLC-PDA-ESI-MS/MS analysis. &lt;strong&gt;Results: &lt;/strong&gt;The ethanol extract of C .inerme leaves showed significant antibacterial activity against &lt;strong&gt;Mycobacterium tuberculosis&lt;/strong&gt;, while that of &lt;em&gt;C. splendens&lt;/em&gt; showed moderate activity. The UPLC-PDA-ESI-MS/MS analysis revealed a total of 36 metabolites detected and tentatively identified in the two species under investigation, among them 28 chromatographic peaks were assigned in&lt;em&gt; C. inerme&lt;/em&gt; while only 14 were assigned in these &lt;em&gt;C. splendens.&lt;/em&gt; The main classes of secondary metabolites detected were Phenylpropanoid and, iridoid glycosides, flavonoids, diterpenoids, phenolic acid and fatty acid derivatives. &lt;strong&gt;Conclusion: &lt;/strong&gt;The results of the antibacterial activity and UPLC-PDA-ESI-MS/ MS analysis showed stronger activity and higher number of metabolites for &lt;em&gt;C. inerme&lt;/em&gt; as compared to &lt;em&gt;C. splendens.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1518</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Hesham I. Elaskary, Omar M. Sabry*, Asmaa M. Khalil, Soheir M. El Zalabani &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, Cairo 11562, EGYPT.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Welly Ratwita</style></author><author><style face="normal" font="default" size="100%">Elin Yulinah Sukandar</style></author><author><style face="normal" font="default" size="100%">I Ketut Adnyana</style></author><author><style face="normal" font="default" size="100%">Neng Fisheri Kurniati</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Alpha Mangostin and Xanthone Activity on Fasting Blood Glucose, Insulin and Langerhans Islet of Langerhans in Alloxan Induced Diabetic Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Fasting blood glucose</style></keyword><keyword><style  face="normal" font="default" size="100%">Insulin plasma</style></keyword><keyword><style  face="normal" font="default" size="100%">Langerhans</style></keyword><keyword><style  face="normal" font="default" size="100%">Xanthone</style></keyword><keyword><style  face="normal" font="default" size="100%">α-mangostin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">64-68</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Objective:&lt;/strong&gt; This research elaborated role of alpha mangostin and xanthone on fasting blood glucose, insulin and langerhans islet in alloxan induced diabetic mice. &lt;strong&gt;Methods:&lt;/strong&gt; Fasting blood glucose, insulin and langerhans islet test were conducted using male &lt;em&gt;Mus musculus&lt;/em&gt; mice, divided into 10 groups randomly, which were normal, control (alloxan induced only), glibenclamide, various doses of α-mangostin and xanthone (5, 10, 20 mg/kgbw). Mice were treated for 21 days. Overnight-fasted mice (12 h) were sacrificed by cervical decapitation on day 21st, following the ethical norms granted by the ethics committee. Fasting blood glucose and insulin plasma were checked. Pancreatic tissues were excised from sacrificed animals, and then fixed in 10 % (v/v) neutral buffered formalin. Histologic observations for Langerhans area were performed after staining using Gomori staining method. &lt;strong&gt;Results:&lt;/strong&gt; The effects of alpha mangostin and xanthone on fasting blood glucose different significantly to control, and were not significantly different from glibenclamide and metformin. Increasing alpha mangostin/xanthone dose from 5 mg/kgbw to 20 mg/bw also did not cause significant differences, although the best results were obtained at a dose of 20 mg/kgbw. Insulin plasma analize showed that there were no significant difference between alpha mangostin/xanthone to normal group, except xanthone 10 mg/kgbw. Langerhans area showed significant difference between alpha mangostin/xanthone to control group. But there’s still had significant difference if we compare to glibenclamid/metformin group.&lt;strong&gt; Conclusion:&lt;/strong&gt; Alpha mangostin and xanthone are two substances that showed antidiabetic effect on fasting blood glucose level, insulin plasma and Langerhans islet.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">64</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Welly Ratwita&lt;sup&gt;*,1&lt;/sup&gt;,&amp;nbsp;Elin Yulinah Sukandar&lt;sup&gt;2&lt;/sup&gt; I Ketut Adnyana&lt;sup&gt;2&lt;/sup&gt; Neng Fisheri Kurniati&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Jenderal Achmad Yani University-Department of Pharmacology and Clinical Pharmacy, School of Pharmacy, Bandung Institute of Technology, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Departement of Pharmacology and Clinical Pharmacy, Bandung Institute of Technology, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Avilekh Naryal</style></author><author><style face="normal" font="default" size="100%">Pushpender Bhardwaj</style></author><author><style face="normal" font="default" size="100%">Anil Kant</style></author><author><style face="normal" font="default" size="100%">OP Chaurasia</style></author><author><style face="normal" font="default" size="100%">Tsering Stobdan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Altitude and Seed Phenotypic Effect on Amygdalin Content in Apricot (Prunus armeniaca L.) Kernel</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Bitterness</style></keyword><keyword><style  face="normal" font="default" size="100%">Cyanide</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevation</style></keyword><keyword><style  face="normal" font="default" size="100%">Ladakh</style></keyword><keyword><style  face="normal" font="default" size="100%">Seed Coat</style></keyword><keyword><style  face="normal" font="default" size="100%">Sweetness</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year></dates><pages><style face="normal" font="default" size="100%">xx-xx</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; Genetic component influencing amygdalin content in apricot kernel is well documented. This study aims to evaluate influence of altitude and seed phenotypic characters on amygdalin content in apricot kernel. &lt;strong&gt;Methods:&lt;/strong&gt; Fruits from 126 genotypes differing in kernel taste and seed coat colour were collected from seven locations from 3008-3346 m asl in trans-Himalaya. Amygdalin content in kernel was determined. &lt;strong&gt;Results:&lt;/strong&gt; Amygdalin content in bitter kernel was significan tly higher (44.6±9.0 mg.g&lt;sup&gt;-1&lt;/sup&gt;) than that of sweet kernel (3.1±1.8 mg.g&lt;sup&gt;-1&lt;/sup&gt;) with brown seed coat. The geographical elevation had no influence on kernel amygdalin content. Similarly, seed and kernel physical characters, except seed coat color, had no significant effect on kernel amygdalin content. High variability within genotypes was observed suggesting that genotype played significant role on amygdalin content in apricot kernel. Low amygdalin content (2.4±1.2 mg.&lt;sup&gt;g-1&lt;/sup&gt;) in apricot kernel with white seed coat phenotype confirmed our earlier finding that the white phenotypic marker is associated with sweet kernel. &lt;strong&gt;Conclusion:&lt;/strong&gt; The geographical elevation had no influence on kernel amygdalin content. White seed coat phenotype can be taken as a marker for low amygdalin content in future studies.&lt;/p&gt;
</style></abstract><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">xx</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Avilekh Naryal&lt;sup&gt;1&lt;/sup&gt;, Pushpender Bhardwaj&lt;sup&gt;1&lt;/sup&gt;, Anil Kant&lt;sup&gt;2&lt;/sup&gt;, OP Chaurasia&lt;sup&gt;1&lt;/sup&gt;, Tsering Stobdan&lt;sup&gt;1* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Defence Institute of High-Altitude Research, Defence Research and Development Organisation, Leh-Ladakh-194101, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Jaypee University of Information Technology, Wakhnaghat, Solan-173215, Himachal Pradesh, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">VV Fedotova</style></author><author><style face="normal" font="default" size="100%">DA Konovalov</style></author><author><style face="normal" font="default" size="100%">АА Kruglaya</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anatomical Study of Pachyphragma macrophyllum (Hoffm.) N. Busch</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Collenchyma</style></keyword><keyword><style  face="normal" font="default" size="100%">Cross-section</style></keyword><keyword><style  face="normal" font="default" size="100%">Mesophyll</style></keyword><keyword><style  face="normal" font="default" size="100%">Outgrowths on the edge of the leaf</style></keyword><keyword><style  face="normal" font="default" size="100%">Pachyphragma macrophyllum</style></keyword><keyword><style  face="normal" font="default" size="100%">Stomata anisocytic type</style></keyword><keyword><style  face="normal" font="default" size="100%">Vascular bundle</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1587-1590</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;&lt;em&gt;Pachyphragma macrophyllum &lt;/em&gt;(&lt;em&gt;Hoffm&lt;/em&gt;.) N. Busch is not studied endemic of the Caucasus (Russia) and Turkey. Now in medicine, it is not applied yet, but preliminary data confirm potential use of this plant. For this purpose, it is necessary to carry out the analysis of &lt;em&gt;P. macrophyllum,&lt;/em&gt; and we began with morphological, anatomic studying. &lt;strong&gt;Materials and Methods:&lt;/strong&gt;&lt;em&gt; P. macrophyllum&lt;/em&gt; herb was collected during the flowering period on the Mount Mashuk in Pyatigorsk, Stavropol region, Russia in April 2019. The anatomical structure of &lt;em&gt;P. macrophyllum &lt;/em&gt;is considered in accordance with the requirements of the State Pharmacopoeia XIV. &lt;strong&gt;Results: &lt;/strong&gt;The main morphological signs of &lt;em&gt;P. macrophyllum: &lt;/em&gt;basal leaves have petioles; cordate or reniform. Stem leaves oval, petioles short. The leaves have a serrated margin. The inflorescences grow in a raceme. Fruit cordate silicula. Microscopic signs: on the edge of the leaf blade are outgrowths, walls of cells of the upper and lower epidermis heavily sinuous, stomata as a rule anisocytic type. In cross-section of the leaf, two types of mesophyll: palisade and spongy; vascular bundle collateral round shape. On the cross-section of the stem, the epidermis, collenchyma, parenchyma, collateral vascular bundles are located around. Cells of epidermis of a petal and sepal of a flower polygonal. &lt;strong&gt;Conclusion: &lt;/strong&gt;The received standards will provide reference information for identification, purity, standardisation for the use of &lt;em&gt;P. macrophyllum &lt;/em&gt;as raw materials for medicines.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1587</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;VV Fedotova, DA Konovalov*, АА Kruglaya&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Pharmacognosy, Botany and Technology of Phytopreparations, Pyatigorsk Medical and Pharmaceutical Institute, a Branch of Volgograd State Medical University Ministry of Health of Russian Federation, Pyatigorsk, 357532, Kalinina 11, RUSSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zulhabri Othman</style></author><author><style face="normal" font="default" size="100%">Hamimi Rasyiqah Hassan Khalep</style></author><author><style face="normal" font="default" size="100%">Azrina Zainal Abidin</style></author><author><style face="normal" font="default" size="100%">Halijah Hassan</style></author><author><style face="normal" font="default" size="100%">Santosh Fattepur</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Anti-Angiogenic Properties of Morinda citrifolia. L (Mengkudu) Leaves Using Chicken Chorioallantoic Membrane (CAM) Assay</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-angiogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Chicken Chorioallantoic Membrane (CAM) assay</style></keyword><keyword><style  face="normal" font="default" size="100%">Morinda citrifolia. L leaves</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical</style></keyword><keyword><style  face="normal" font="default" size="100%">White Leghorn eggs</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">12-15</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Background:&lt;/strong&gt; Anti-angiogenesis or inhibition of blood vessel formation is the best way to prevent the growth and metastasis of tumors. The use &lt;em&gt;Morinda citrifolis.&lt;/em&gt; L extracts have been reported to exhibit a broad range of therapeutic effects, including antibacterial and antitumor. Objective: This study aims to investigate the anti-angiogenic properties of &lt;em&gt;Morinda citrifolia&lt;/em&gt;. L leaves extracts using Chicken Chorioallantoic Membrane (CAM) assay. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The Fertile White Leghorn eggs were divided into five groups which were control, Bevacizumab drug and treatment groups with 25%, 50% and 75% of &lt;em&gt;Morinda citrifolia&lt;/em&gt;. L leaves extracts respectively. The reduction of the blood vessel was counted after 12 h and 24 h post-treatment. &lt;strong&gt;Results:&lt;/strong&gt; Analysis have shown significant differences (&lt;em&gt;P&lt;/em&gt;&amp;lt;0.05) in the reduction of the blood vessel between each group at 24 h post-treatment. The group with 75% extracts showed 37.1% reductions of blood vessel compared to groups 50% and 25% extracts which showed 4% and 12.8% respectively. The phytochemical screening has showed that &lt;em&gt;Morinda citrifolia&lt;/em&gt;. L leaves extracts was positive for flavonoid, phenols and phytosterols. &lt;strong&gt;Conclusion:&lt;/strong&gt; &lt;em&gt;Morinda citrifolia&lt;/em&gt;. L leaves extracts consist of the phytochemical compounds that have the ability to inhibit the angiogenesis.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">12</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Zulhabri Othman&lt;sup&gt;1,2*&lt;/sup&gt;, Hamimi Rasyiqah Hassan Khalep&lt;sup&gt;1&lt;/sup&gt;, Azrina Zainal Abidin&lt;sup&gt;1&lt;/sup&gt;, Halijah Hassan&lt;sup&gt;1&lt;/sup&gt;, Santosh Fattepur&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Diagnostic and Allied Health Science, Faculty of Health and Life Sciences, Management and Science University, 40100 Shah Alam, Selangor, MALAYSIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;School of Graduate Studies, Post-Graduate Centre, Management and Science University, MALAYSIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;School of Pharmacy, Management and Science University, 40100 Shah Alam, Selangor, MALAYSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Andi Hamdillah</style></author><author><style face="normal" font="default" size="100%">Alim Isnansetyo</style></author><author><style face="normal" font="default" size="100%">Indah Istiqomah</style></author><author><style face="normal" font="default" size="100%">Indun Dewi Puspita</style></author><author><style face="normal" font="default" size="100%">Desy Putri Handayani</style></author><author><style face="normal" font="default" size="100%">Takushi Kaneko</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antibacterial Activity of Coastal Plants and Marine Sponges from Kei Island Indonesia against Bacterial Fish Pathogens</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Bacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">Coastal plant</style></keyword><keyword><style  face="normal" font="default" size="100%">Fish pathogen</style></keyword><keyword><style  face="normal" font="default" size="100%">Marine sponge</style></keyword><keyword><style  face="normal" font="default" size="100%">Secondary metabolite</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">812-817</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; The objective of this study was to investigate the antibacterial activity of coastal plants and marine sponges extracts against fish bacterial pathogens. &lt;strong&gt;Methods:&lt;/strong&gt; Samples were extracted by maceration and the extracts were examined for their antibacterial activities against &lt;em&gt;Streptococcus&lt;/em&gt; sp. BJ0509, &lt;em&gt;Staphylococcus aureus&lt;/em&gt; ATCC 6538,&lt;em&gt; Aeromonas hydrophila&lt;/em&gt; BA03 and &lt;em&gt;Vibrio parahaemolyticus&lt;/em&gt; 29S by means of paper disc diffusion method. Active extracts were partitioned and purified by column chromatography. The purified substance was tested for Minimum Inhibitory Concentration (MIC) against seven bacterial fish pathogens namely&lt;em&gt; Streptococcus &lt;/em&gt;sp., &lt;em&gt;Vibrio parahaemolyticus&lt;/em&gt;, &lt;em&gt;V. alginolyticus, V. harveyi, Photobacterium damselae, Aeromonas hydrophila and A. dhakensis.&lt;/em&gt; &lt;strong&gt;Results: &lt;/strong&gt;The highest antibacterial activity against all bacteria used in the assay was demonstrated by OKA 6, a bark extract sample of a coastal plant, &lt;em&gt;Diospyros maritima.&lt;/em&gt; It showed a diameter of inhibition zones against &lt;em&gt;Streptococcus &lt;/em&gt;sp. BJ0509, &lt;em&gt;S. aureus&lt;/em&gt; ATCC 6538, &lt;em&gt;A. hydrophila&lt;/em&gt; BA03 and &lt;em&gt;V. parahaemolyticus&lt;/em&gt; 29S of 19, 33, 18, and 18 mm, respectively. The column chromatography fraction of OKA 6 inhibited the growth of &lt;em&gt;S. aureus&lt;/em&gt; ATCC 6538 with MIC of 3.125 μg/mL. The MIC of this fraction against seven bacterial fish pathogens ranged &amp;lt; 0.098 to 3.125 μg/mL. The antibacterial activity of partially purified substance obtained from column chromatography fractionation of OKA 6 was higher than those of oxytetracycline and kanamycin. &lt;strong&gt;Conclusions: &lt;/strong&gt;This result indicates that antibacterial activity of the partially purified substance is potentially higher than those of the commercial antibiotics tested. It further indicates that OKA 6 extract from &lt;em&gt;D. maritima&lt;/em&gt; can serve as a promising resource for the development of therapeutic agents against bacterial infections in aquaculture.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">812</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Andi Hamdillah&lt;sup&gt;1&lt;/sup&gt;, Alim Isnansetyo&lt;sup&gt;1,*&lt;/sup&gt;, Indah Istiqomah&lt;sup&gt;1&lt;/sup&gt;, Indun Dewi Puspita&lt;sup&gt;1&lt;/sup&gt;, Desy Putri Handayani&lt;sup&gt;1&lt;/sup&gt;, Takushi Kaneko&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Fisheries, Faculty of Agriculture, Universitas Gadjah Mada, Jl. Flora, Bulaksumur, Yogyakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Global Alliance for TB Drug Development, Research and Development, 40 Wall Street, 24&lt;sup&gt;th&lt;/sup&gt; Floor, New York, NY, USA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ahmed Al-Ghamdi</style></author><author><style face="normal" font="default" size="100%">Thanaa Elkholy</style></author><author><style face="normal" font="default" size="100%">Shahd Abuhelal</style></author><author><style face="normal" font="default" size="100%">Hatim Al-Abbadi</style></author><author><style face="normal" font="default" size="100%">Dina Qahwaji</style></author><author><style face="normal" font="default" size="100%">Nahlaa Khalefah</style></author><author><style face="normal" font="default" size="100%">Hanaan Sobhy</style></author><author><style face="normal" font="default" size="100%">Mohammad Abu-Hilal</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antibacterial and Antifungal Activity of Jojoba Wax Liquid (Simmondsia chinensis)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial</style></keyword><keyword><style  face="normal" font="default" size="100%">Antimicrobial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Jojoba oil</style></keyword><keyword><style  face="normal" font="default" size="100%">Minimum inhibitory concentration (MIC)</style></keyword><keyword><style  face="normal" font="default" size="100%">Simmondsia chinesisis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">191-194</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;!-- x-tinymce/html --&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: Plants are a rich source of bioactive compounds. &lt;em&gt;Simmondsia chinensis&lt;/em&gt;, also known as Jojoba, is the sole member the Simmondsiaceae’s family and has been known traditionally for many medical uses. Objectives: Herein we evaluate the value of crude jojoba oil (J.O) as an antimicrobial agent in vitro.&lt;strong&gt; Methods&lt;/strong&gt;: J.O was tested for potential antimicrobial activity against &lt;em&gt;Bacillus subtilis&lt;/em&gt;, &lt;em&gt;Staphylococcus aureus, Proteus vulgaris, P. mirabilis, Salmonella typhimurium, Escherichia coli, Pseudomonas aeruginosa, Candida albicans and Asperigillus flavus&lt;/em&gt;. &lt;strong&gt;Results&lt;/strong&gt;: Our results did not show any effect on fungi or yeast. However, a significant antibacterial activity was observed against &lt;em&gt;B. subtilis, S. aureus, P. vulgaris, P. mirabilis&lt;/em&gt;. A high activity was observed for J.O at Minimum inhibitory concentration (MIC) level of 12.5 mg/ml. Interestingly, &lt;em&gt;S. typhimurium, E. coli and Ps. aeruginosa&lt;/em&gt; were found to be highly resistant. &lt;strong&gt;Conclusion&lt;/strong&gt;: Our findings suggest that J.O may have a medicinal potential as natural antibacterial agent.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">191</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;!-- x-tinymce/html --&gt;&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Ahmed Al-Ghamdi&lt;sup&gt;1,&lt;/sup&gt;*, Thanaa Elkholy&lt;sup&gt;2&lt;/sup&gt;, Shahd Abuhelal&lt;sup&gt;3&lt;/sup&gt;, Hatim Al-Abbadi&lt;sup&gt;4&lt;/sup&gt;, Dina Qahwaji&lt;sup&gt;5&lt;/sup&gt;, Nahlaa Khalefah&lt;sup&gt;5&lt;/sup&gt;, Hanaan Sobhy&lt;sup&gt;6&lt;/sup&gt;, Mohammad Abu-Hilal&lt;sup&gt;7&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, SAUDI ARABIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Al-Azhar University, Al Mokhaym Al Daem, Cairo, Cairo Governorate, EGYPT.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Institute of Pharmaceutical Science, Faculty of Life Sciences and Medicine, King’s College London, Franklin-Wilkins building, 150 Stamford Street, London SE1 8NH, UNITED KINGDOM.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Consultant General Laparoscopic Surgeon, King Abdulaziz University, University Hospital, Director of Experimental Surgery Unit, KFMRC*, Jeddah, SAUDI ARABIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;5&lt;/sup&gt;Departments of Clinical Nutrition, Faculty of Applied Medical Sciences, King Abdul-Aziz University, Jeddah, SAUDI ARABIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;6&lt;/sup&gt;Head of Pharmacology Unit, -Biochemical, and Toxicology and Food Deficiency.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;7&lt;/sup&gt;Consultant Hepatobiliary and Pancreatic Surgery, University Hospital, Southampton University, UNITED KINGDOM.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sachin Chaudhary</style></author><author><style face="normal" font="default" size="100%">Harish Chandra Verma</style></author><author><style face="normal" font="default" size="100%">Mandeep Kumar Gupta</style></author><author><style face="normal" font="default" size="100%">Hitesh Kumar</style></author><author><style face="normal" font="default" size="100%">Sudhansu Ranjan Swain</style></author><author><style face="normal" font="default" size="100%">Ramesh Kumar Gupta</style></author><author><style face="normal" font="default" size="100%">Abdel-Nasser El-Shorbagi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antidiabetic Aptitude of Cordia sebestena and its Outcome on Biochemical Parameters, Serum Electrolytes, and Hematological Markers</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anemia</style></keyword><keyword><style  face="normal" font="default" size="100%">Antidiabetic</style></keyword><keyword><style  face="normal" font="default" size="100%">Cordia sebestena</style></keyword><keyword><style  face="normal" font="default" size="100%">Glucose</style></keyword><keyword><style  face="normal" font="default" size="100%">Streptozotocin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">418-423</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; The present study investigated the antidiabetic outcome of ethanolic extract of &lt;em&gt;Cordia sebestena&lt;/em&gt; fruit (EECSF) in streptozotocin (STZ)-induced diabetogenic rodents and evaluated its consequence to improve the level of biochemical parameters, serum electrolytes level, and hematological indices along with its impact on body weight. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The albino rodents were selected to observe oral glucose tolerance test by oral intake of aqueous glucose solution (4 g/kg, body weight) in normal rodents and assessment of blood glucose level after administration of EECSF at 100 and 200 mg/kg and standard drug glibenclamide at 0.6 mg/kg, body weight. Antidiabetic activity was estimated in the chronic biological model by STZ (65 mg/kg/i.p.)-induced diabetes in rodents escorted by the determination of blood glucose. Further pharmacological research was carried out to explore the effect of EECSF on body weight, variations in biochemical parameters including aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, total bilirubin, and total protein, transformations in serum electrolytes such as Na&lt;sup&gt;+&lt;/sup&gt;, K&lt;sup&gt;+&lt;/sup&gt;, Cl&lt;sup&gt;−&lt;/sup&gt;, and Ca&lt;sup&gt;2+&lt;/sup&gt; along with estimation of hematological indices such as red blood cells, white blood cells, hemoglobin, lymphocytes, neutrophils, eosinophils, and monocytes. &lt;strong&gt;Results:&lt;/strong&gt; It was discovered that EECSF significantly lowered the blood glucose level of diabetic rodents along with enhancement in body weight. Correspondingly, EECSF significantly ameliorated the biochemical parameters, serum electrolytes, and hematological indices. &lt;strong&gt;Conclusion:&lt;/strong&gt; The results demonstrated the antidiabetic potential of EECSF in STZ-induced diabetes in rodents, and it could be selected to benefit from diabetes and its affiliated complexities inclusive of anemia, diabetic nephropathy, retinopathy, neuropathy, and hepatitis.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">418</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Sachin Chaudhary&lt;sup&gt;1&lt;/sup&gt;, Harish Chandra Verma&lt;sup&gt;2&lt;/sup&gt;, Mandeep Kumar Gupta&lt;sup&gt;2&lt;/sup&gt;, Hitesh Kumar&lt;sup&gt;2&lt;/sup&gt;, Sudhansu Ranjan Swain&lt;sup&gt;2&lt;/sup&gt;, Ramesh Kumar Gupta&lt;sup&gt;2&lt;/sup&gt;, Abdel-Nasser El-Shorbagi&lt;sup&gt;1,3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Medicinal Chemistry, College of Pharmacy, University of Sharjah, UNITED ARAB EMIRATES.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Chemistry and Pharmaceutics, Moradabad Educational Trust, Group of Institutions, Faculty of Pharmacy, Uttar Pradesh, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Sharjah Institute for Medical Research, University of Sharjah, Sharjah, UNITED ARAB EMIRATES.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rohan S. Phatak</style></author><author><style face="normal" font="default" size="100%">Chitra C. Khanwelkar</style></author><author><style face="normal" font="default" size="100%">Somnath M. Matule</style></author><author><style face="normal" font="default" size="100%">Kailas D. Datkhile</style></author><author><style face="normal" font="default" size="100%">Anup S. Hendre</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antihyperlipidemic Activity of Murraya koenigii Leaves Methanolic and Aqueous Extracts on Serum Lipid Profile of High Fat-Fructose Fed Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Atherogenic index</style></keyword><keyword><style  face="normal" font="default" size="100%">High fat-fructose diet</style></keyword><keyword><style  face="normal" font="default" size="100%">Hyperlipidemia</style></keyword><keyword><style  face="normal" font="default" size="100%">lipid profile</style></keyword><keyword><style  face="normal" font="default" size="100%">Murraya Koenigii</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">836-841</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Dyslipidemia has been considered as one of coronary risk factors contributing to the cardiovascular diseases. The beneficial effects of &lt;em&gt;Murraya koenigii&lt;/em&gt; leaf on HFFD induced hyperlipidemia in rats has been very less reported in the recent review of literature.&lt;strong&gt; Aim and Objectives:&lt;/strong&gt; To study the hypolipidemic activity of &lt;em&gt;Murraya koenigii&lt;/em&gt; leaves on the serum lipid profile in HFFD rat model. &lt;strong&gt;Material and Methods:&lt;/strong&gt; Thirty-six rats of either sex were randomly divided into six groups of six animals each. HFFD was fed p.o to all rats from Groups I, II, IV, V and VI except Group III throughout the period of 14 weeks. Group III rats received normal diet and water &lt;em&gt;ad libitum &lt;/em&gt;only. Group I, II, IV and V were treated respectively with AEMK (200 mg/kg/day, p. o), MEMK (200 mg/kg/day, p. o), MET (50 mg/kg/day, p. o) and ATO (10 mg/kg/day, p. o). On the last day of experimental study, blood was collected by retro-orbital puncture method. BSL and lipid profile were assessed. &lt;strong&gt;Results: &lt;/strong&gt;Elevated levels of TC, TG, LDL-C, VLDL-C and diminished level of HDL-C were observed in group VI. &lt;em&gt;Murraya koenigii&lt;/em&gt; leaves extract exhibited significant hypolipidemic effect on serum TC and LDL-C in rats owing to its hypocholesterolemic properties. AIP was highly significant in both of AEMK and MEMK extracts. &lt;strong&gt;Conclusion:&lt;/strong&gt; Results of the present study have suggested that the antihyperlipidemic activity of &lt;em&gt;Murraya koenigii&lt;/em&gt; leaves leading to decrease in serum lipid parameters mainly TC, LDL-C along with atherogenic risk might be due to its presence of bioactive compounds.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">836</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Rohan S. Phatak&lt;sup&gt;1,*&lt;/sup&gt;, Chitra C. Khanwelkar&lt;sup&gt;1&lt;/sup&gt;, Somnath M. Matule&lt;sup&gt;1&lt;/sup&gt;, Kailas D. Datkhile&lt;sup&gt;2&lt;/sup&gt;, Anup S. Hendre&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Krishna Institute of Medical Sciences, Karad-415110, Maharashtra, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Molecular Biology and Genetics, Krishna Institute of Medical Sciences, Karad-415110, Maharashtra, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Biochemistry, Krishna Institute of Medical Sciences, Karad-415110, Maharashtra, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Luján-Carpio Elmer</style></author><author><style face="normal" font="default" size="100%">Medina-Salazar Henry</style></author><author><style face="normal" font="default" size="100%">Mayor-Vega Alexander</style></author><author><style face="normal" font="default" size="100%">Medrano-Canchari Karola</style></author><author><style face="normal" font="default" size="100%">Mazuelos-Rivas María</style></author><author><style face="normal" font="default" size="100%">Lizarraga-Castañeda Zaida</style></author><author><style face="normal" font="default" size="100%">Pante-Medina Carlos</style></author><author><style face="normal" font="default" size="100%">Salazar-Granara Alberto</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anti-Inflammatory and Neurobehavioral Effects of the Leaves from Maytenus macrocarpa (Ruiz and Pavon) Briquet in Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammation</style></keyword><keyword><style  face="normal" font="default" size="100%">Diclofenac</style></keyword><keyword><style  face="normal" font="default" size="100%">Leaves</style></keyword><keyword><style  face="normal" font="default" size="100%">Maytenus</style></keyword><keyword><style  face="normal" font="default" size="100%">Mice</style></keyword><keyword><style  face="normal" font="default" size="100%">Neurobehavioral manifestations</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">75-80</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Context:&lt;/strong&gt; &lt;em&gt;Maytenus macrocarpa&lt;/em&gt; (Chuchuhuasi) has long been employed in Peru as a traditional alternative therapy for several diseases, including cancer, arthritis and diarrhea. Recent studies show that several species of Maytenus have effects on nociceptive and inflammatory signaling, as well as toxic effects on behavioral neuronal pathways.&lt;strong&gt; Aims:&lt;/strong&gt; The aim of this study is to evaluate the anti-inflammatory effects and neurobehavioral side manifestations of the leaf of&lt;em&gt; Maytenus macrocarpa&lt;/em&gt; (Ruiz and Pavón) Briquet. &lt;strong&gt;Methods and Materials:&lt;/strong&gt; Experimental study, double blind. 60 male albino mice strain Balb/c were divided in ten groups and each group, was orally feed with different doses of ethanolic extracts of &lt;em&gt;Maytenus macrocarpa&lt;/em&gt; (500, 750, 1000, 1250 and 1500 mg/kg), others group received distilled water, caffeine 32 mg/kg, diazepam 32 mg/kg, diclofenac 15 mg/kg and the last group without substance. Neurobehavioral effects were assessed by the Irwin test. The anti-inflammatory activity was measured by the Carrageenan paw oedema test. Statistical analysis was performed with ANOVA test and Fisher exact test. &lt;strong&gt;Results:&lt;/strong&gt; Anti-inflammatory effects of &lt;em&gt;M. macrocarpa&lt;/em&gt; were observed in a non-significant trend of dose dependent form. &lt;em&gt;M. macrocarpa&lt;/em&gt; displayed an anti-inflammatory effect at 1250 mg/kg and these effects were higher in comparison with diclofenac (74.14% vs 58.62%, one way ANOVA, &lt;em&gt;p&lt;/em&gt;&amp;lt;0.05). Neurobehavioral side effects secondary to &lt;em&gt;M. macrocarpa&lt;/em&gt; therapy were also identified, these included excitation, abnormal gait, abdominal cramps, piloerection, stereotypes and scratching (Fisher exact, p&amp;lt;0.05, CI 95%). &lt;strong&gt;Conclusion:&lt;/strong&gt; &lt;em&gt;M. macrocarpa&lt;/em&gt; leaves presented anti-inflammatory activity and concomitants neurobehavioral side effects.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">75</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Luján-Carpio Elmer&lt;sup&gt;1,2&lt;/sup&gt;, Medina-Salazar Henry&lt;sup&gt;1,2&lt;/sup&gt;, Mayor-Vega Alexander&lt;sup&gt;1,2&lt;/sup&gt;, Medrano-Canchari Karola&lt;sup&gt;1&lt;/sup&gt;, Mazuelos-Rivas María&lt;sup&gt;1&lt;/sup&gt;, Lizarraga-Castañeda Zaida&lt;sup&gt;1,2&lt;/sup&gt;, Pante-Medina Carlos&lt;sup&gt;1&lt;/sup&gt;, Salazar-Granara Alberto&lt;sup&gt;1,2,* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Universidad de San Martín de Porres. Facultad de Medicina Humana. Instituto de Investigación, Centro de Investigación de Medicina Tradicional y Farmacología. Lima, PERÚ.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Sociedad Científica de Estudiantes de Medicina de la Universidad de San Martin de Porres. Lima, PERÚ.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kartini Kartini</style></author><author><style face="normal" font="default" size="100%">Christina Avanti</style></author><author><style face="normal" font="default" size="100%">Chutima Phechkrajang</style></author><author><style face="normal" font="default" size="100%">Omboon Vallisuta</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antioxidant Activity, HPTLC Fingerprint and Discriminant Analysis of Plantago major Leaves from Diverse Origins in Indonesia</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chemometrics</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Herbal medicines</style></keyword><keyword><style  face="normal" font="default" size="100%">Pattern-oriented</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolics</style></keyword><keyword><style  face="normal" font="default" size="100%">PLSDA</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1483-1489</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Plantago major &lt;/em&gt;L. (&lt;em&gt;Plantaginaceae&lt;/em&gt;) is a perennial herb having contribution to the folk medicine all around the world, including Indonesia with wide geographical distribution. Plant materials origin is one factor that significantly influences the quality of herbal medicines. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; In this paper, High-Performance Thin Layer Chromatography (HPTLC) method using pattern-oriented approach has been employed to evaluate the quality of &lt;em&gt;Plantago major&lt;/em&gt; leaves collected from seven origins in Indonesia. To differentiate the antioxidant capacities of those plant materials, the crude extracts were tested using 1,1-diphenyl-2-picrylhydrazyl (DPPH), total phenolics, and total flavonoids assay methods. &lt;strong&gt;Results:&lt;/strong&gt; The results showed that radical scavenging activity, total phenolics, and total flavonoids of plant material from seven origins were significantly different. Moreover, HPTLC fingerprints analyzed with chemometrics showed an ability to discriminate the leaves samples from various origins as well as detect chemicals responsible for discrimination. Two models using principal component analysis (PCA) and partial least squares (PLS-DA) were built in chemometrics test. The PCA model was able to describe the studied samples by using four principal components with a value of explained variance of 95%, whereas PLS-DA model accurately classified the leaves samples with prediction ability of 100%. In the PCA, loading plot of the first PC showed that peaks number 10 and 12 are the most important peaks for clustering of the samples. &lt;strong&gt;Conclusions: &lt;/strong&gt;&lt;em&gt;Plantago major &lt;/em&gt;collected from different origins revealed different radical scavenging activity and concentration of total phenolics as well as total flavonoids. HPTLC fingerprints coupled with chemometrics analysis can be used as an alternative to marker-oriented method for the quality control of &lt;em&gt;Plantago major&lt;/em&gt;.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1483</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kartini Kartini&lt;sup&gt;1,&lt;/sup&gt;*, Christina Avanti&lt;sup&gt;2&lt;/sup&gt;, Chutima Phechkrajang&lt;sup&gt;3&lt;/sup&gt;, Omboon Vallisuta&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Biology, Faculty of Pharmacy, University of Surabaya, Raya Kalirungkut Road, Surabaya 60293, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutic, Faculty of Pharmacy, University of Surabaya, Raya Kalirungkut Road, Surabaya 60293, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Mahidol University, 447 Sri-Ayudhaya Road, Ratchathewi, Bangkok 10400, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacognosy, Faculty of Pharmacy, Mahidol University, 447 Sri-Ayudhaya Road, Ratchathewi, Bangkok 10400, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nagarajan Keerthiga</style></author><author><style face="normal" font="default" size="100%">Roy Anitha</style></author><author><style face="normal" font="default" size="100%">S Rajeshkumar</style></author><author><style face="normal" font="default" size="100%">Thangavelu Lakshmi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antioxidant Activity of Cumin Oil Mediated Silver Nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">AgNP</style></keyword><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Biosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Cumin oil</style></keyword><keyword><style  face="normal" font="default" size="100%">Nanoparticles</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">787-789</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Aim: &lt;/strong&gt;The aim of the study was to employ cumin oil in the synthesis of silver nanoparticles and check the antioxidant activity of the cumin oil mediated silver nanoparticles. &lt;strong&gt;Background:&lt;/strong&gt; The introduction of Nanoparticles (NPs) has revolutionized every field including medicine, nutrition and energy. The use of nanotechnology in medicine especially for drug delivery is shown to have various benefits. Nanoparticles are being used to reduce toxicity and side effects that drugs may impose to the patient. Cumin (&lt;em&gt;Cuminum cyminum&lt;/em&gt;) is a common spice used for its distinct aromatic effect. Plant mediated biological synthesis of nanoparticles has been gaining importance due to its simplicity and eco friendliness. This study therefore was aimed to synthesize cumin oil mediated silver nanoparticles and assess its antioxidant activity. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Cumin oil mediated silver nanoparticles were initially synthesised and characterised by UV-Visible spectrophotometer and TEM. Further the cumin oil mediated AgNPs were subjected to DPPH assay to determine the antioxidant activity. &lt;strong&gt;Results: &lt;/strong&gt;Cumin oil mediated AgNPs were biosynthesised with ease and showed good antioxidant activity compared to standard. &lt;strong&gt;Conclusion:&lt;/strong&gt; This study conclude that cumin seed oil mediated silver nanoparticles have the potential to be used as an effective antioxidant. Hence, it may be employed in large scale production and may be used in many medicinal applications where there is a need for antioxidant.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Research Study</style></work-type><section><style face="normal" font="default" size="100%">787</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nagarajan Keerthiga, Roy Anitha*, S Rajeshkumar, Thangavelu Lakshmi &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Saveetha Dental College, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rasmita Jena</style></author><author><style face="normal" font="default" size="100%">Durga Madhab Kar</style></author><author><style face="normal" font="default" size="100%">Diptirani Rath</style></author><author><style face="normal" font="default" size="100%">Kaushik Sur Roy</style></author><author><style face="normal" font="default" size="100%">Goutam Ghosh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antiulcer Property of Mussaenda philippica</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-secretory</style></keyword><keyword><style  face="normal" font="default" size="100%">Gastric volume</style></keyword><keyword><style  face="normal" font="default" size="100%">Methanol extracts</style></keyword><keyword><style  face="normal" font="default" size="100%">Mussaenda philippica</style></keyword><keyword><style  face="normal" font="default" size="100%">Pylorus ligation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">603-607</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Mussaenda philippica &lt;/em&gt;(Rubiaceae) is a shrub distributed in all the planes of India, Philippines and South-East Asia. Its synonyms are &lt;em&gt;M. grandiflora, M. acutifolia, M. frondosa&lt;/em&gt; etc. The plant is preferred as medication for the treatment of jaundice, dysentery, stomachache and influenza. The current study was based on the evaluation of antiulcer property of &lt;em&gt;M. philippica &lt;/em&gt;leaves extract. &lt;strong&gt;Methods:&lt;/strong&gt; The methods used were pylorus ligated, ethanol induced and 0.2(M) NaOH induced ulcer in rats. &lt;strong&gt;Results:&lt;/strong&gt; In pylorus ligation model, aqueous extract (200 mg/kg) produced a substantial reduction in ulcer index followed by decrease in gastric volume, total acidity associated with a raise in pH, which, confirmed that tested extract of the plant act by altering the mucosal barrier Thus, the gastro protective effect of this extract may be due to the presence of flavonoid in the plant. In the same way, aqueous extract of the plant showed significant effect against ethanol induced gastric ulcer in rat as compared to methanol-treated group, which, may be due to leukotriene antagonistic effect or the inhibition of 5-lipooxygenase pathway. In NaOH induced ulcer model, aqueous extract of &lt;em&gt;M. philippica &lt;/em&gt;revealed significant antiulcer effects on the basis of pH effect and ulcer index in rats. The anti-ulcerogenic and anti-secretory effect of the tested &lt;em&gt;M. philippica&lt;/em&gt; leaves extracts point out its possible cyto-protective effect. &lt;strong&gt;Conclusion:&lt;/strong&gt; In conclusion the aqueous extract of &lt;em&gt;M. philippica &lt;/em&gt;leaves possess potential antiulcer activity in experimental rat models.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">603</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Rasmita Jena*, Durga Madhab Kar, Diptirani Rath, Kaushik Sur Roy, Goutam Ghosh &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Pharmacology, School of Pharmaceutical Sciences, S ‘O’ A Deemed to be University, Bhubaneswar, Odisha– 751003, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Susha Antony</style></author><author><style face="normal" font="default" size="100%">Kunnambath Krishna Kumar</style></author><author><style face="normal" font="default" size="100%">Jalaja Sudhi Menon</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Assessment of Phyto-Constituents by GC-MS and Anti-Tumour Activity of Garlic Grown in Different Altitude: A Comparative Study</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-tumour</style></keyword><keyword><style  face="normal" font="default" size="100%">Garlic oil</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS</style></keyword><keyword><style  face="normal" font="default" size="100%">MTT</style></keyword><keyword><style  face="normal" font="default" size="100%">Phyto-constituents</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">350-354</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Garlic (&lt;em&gt;Allium sativum&lt;/em&gt; L.) is most important spice containing highest sources of total phenolic compounds. It has been used as a component of traditional and modern medicine. Pharmacological properties of garlic is mainly depend on its phyto-constituents content, which varies between geographical regions. The aim of this study was to evaluate and compare the phyto-constituents content of garlic sample collected from high ranges of Idukki (Kanthallur) with that of Tamil Nadu (Mettupalayam market) garlic sample. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; garlic clove sample were collected from high ranges of kanthallur region (GSK) and Mettupalayam region (GSM). The garlic oil was extracted from the collected garlic sample by solvent extraction method. The phytochemical study of extracted garlic oil were conducted using standard methods of analysis and subjected GC-MS analysis. Further, the extracted oil samples were studied for their anti-tumour activity against Dalton Lymphoma Cell Lines (DLA) in an &lt;em&gt;in vitro&lt;/em&gt; model. &lt;strong&gt;Results:&lt;/strong&gt; The obtained results revealed that garlic oil of GSK showed highest percentage of yield of oil (1.1%) than garlic oil of GSM (0.6%). The phytochemical screening of GSK indicated the presence of alkaloids and flavonoid, whereas GSM showed presence of alkaloids only. GC-MS analysis of garlic oil study indicated that garlic oil of GSK was found to have eugenol as a novel source compared with garlic oil of GSM. Garlic oil of GSK showed significant anti-tumour activity against DLA cells, compared with garlic oil of GSM.&lt;strong&gt; Conclusion:&lt;/strong&gt; Garlic oil of GSK exhibited potential anti-tumour activity against DLA cells due to presence of eugenol compound as novel source.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">350</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Susha Antony&lt;sup&gt;1&lt;/sup&gt;, Kunnambath Krishna Kumar&lt;sup&gt;1,2,*&lt;/sup&gt;, Jalaja Sudhi Menon&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Chemistry, St James College of Pharmaceutical Sciences, Chalakudy, Kerala, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;St James Hospital Trust Pharmaceutical Research Centre (DSIR Recognized), Chalakudy, Kerala, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Kerala Agriculture University, College of horticulture, Vellanikkara, Trissur, Kerala, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rifki Febriansah</style></author><author><style face="normal" font="default" size="100%">Titi Komalasari</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Co-Chemotherapeutic Effect of Ageratum conyzoides L. Chloroform Fraction and 5-Fluorouracil on Hela Cell Line</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ageratum conyzoides L.</style></keyword><keyword><style  face="normal" font="default" size="100%">Bcl-XL protein</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxic assay</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword><keyword><style  face="normal" font="default" size="100%">Nobiletin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">913-918</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; This study was to determine the co-chemotherapeutic effect of the chloroform fraction of bandotan (&lt;em&gt;Ageratum conyzoides&lt;/em&gt; L.) (CFB) and its combination with 5-Fluorouracil (5-FU) by&lt;em&gt; in vitro&lt;/em&gt; and&lt;em&gt; in silico &lt;/em&gt;assay. &lt;strong&gt;Methods:&lt;/strong&gt; Ethanolic extract of bandotan were fractionated with chloroform. Thin Layer Chromatography (TLC) used to identify active compound and &lt;em&gt;in vitro&lt;/em&gt; study with MTT Assay to determine the viability of HeLa cells after extract treatment.&lt;em&gt; Molecular docking&lt;/em&gt; used Autodock Vina for &lt;em&gt;in silico&lt;/em&gt; study to visualize molecular interaction and affinity between nobiletin and 5-FU with Bcl-XL protein. &lt;strong&gt;Results:&lt;/strong&gt; The result of TLC for CFB showed the Rf value of 0.75, it has the similar value with quersetin standard and indicated that CFB contains flavonoid compound. The &lt;em&gt;Molecular docking&lt;/em&gt; had ΔG for nobiletin and 5-FU were -8.0 and -4.7 kcal/mol, respectively. This result showed that the affinity of nobiletin with Bcl-XL protein higher than 5-FU. Single cytotoxic assay of CFB and 5-FU showed the IC&lt;sub&gt;50&lt;/sub&gt; value of 30 μg/ml and 45 μg/ml, respectively. Combination assay of CFB and 5-FU showed the CI value of 0.36, meaning the presence of synergistic effects. &lt;strong&gt;Conclusion:&lt;/strong&gt; CFB has a positive effect to inhibit viability of HeLa cervical cancer cells and potential to develop as co-chemotherapy agent with 5-FU.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">913</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Rifki Febriansah*, Titi Komalasari&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;School of Pharmacy, Faculty of Medicine and Health Sciences, Universitas Muhammadiyah Yogyakarta, Yogyakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Rahyussalim</style></author><author><style face="normal" font="default" size="100%">Rizky Priambodo Wisnubaroto</style></author><author><style face="normal" font="default" size="100%">Dilla Firzani</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Combination of Spirulina Extract and Sambiloto Effect Histopathologically on Medial Colon from Plasmodium berghei Anka Infected Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Malaria</style></keyword><keyword><style  face="normal" font="default" size="100%">Medial colon</style></keyword><keyword><style  face="normal" font="default" size="100%">Plasmodium berghei Anka</style></keyword><keyword><style  face="normal" font="default" size="100%">Sambiloto</style></keyword><keyword><style  face="normal" font="default" size="100%">Spirulina</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">564-569</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Malaria is one of the biggest burden in medical section in Indonesia, as the prevalence is still high and half of the provinces in Indonesia considered as endemic area.&lt;sup&gt;1-4&lt;/sup&gt; Moreover, the drug resistant case number has grown larger within years.&lt;sup&gt;3-7&lt;/sup&gt; Indonesian people are very close with traditional drug regiment that derived from plants, for example &lt;em&gt;Sambiloto&lt;/em&gt; and &lt;em&gt;Spirulina.&lt;/em&gt;&lt;sup&gt;7-9 &lt;/sup&gt;This research done in order to see the effect of &lt;em&gt;Sambiloto and Spirulina&lt;/em&gt; combination from histopathologic aspect in medial colon of &lt;em&gt;P. berghei &lt;/em&gt;infected mice. &lt;strong&gt;Method:&lt;/strong&gt; The data taken from experimental study using male Swiss Webster mice that has been infected with &lt;em&gt;Plasmodium berghei &lt;/em&gt;Anka. The four groups of mice were given different treatment. The first group treated with &lt;em&gt;Sambiloto &lt;/em&gt;only, the second one with &lt;em&gt;Sambiloto&lt;/em&gt; and Spirulina extract, the third group with &lt;em&gt;Sambiloto and &lt;/em&gt;Spirulina powder and the last one the control group with administration of DHP. &lt;strong&gt;Results:&lt;/strong&gt; The result shows that the group with extract and powder spirulina show a significant result in the inflammatory focus and angiogenesis. However, this research does not necessarily prove the correlation between &lt;em&gt;Sambiloto&lt;/em&gt;-Spirulina and their effect on the goblet cell and dysplasia grade on the infected mice, as the result for both category is insignificant. &lt;strong&gt;Conclusion: &lt;/strong&gt;The study showed that spirulina has positive effect on inflamatory focus and angiogenesis, but the goblet cells count and dysplasia grade result is not noteworthy, as it requires prolonged inflammation process in order to achieve the optimal result.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">564</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kusmardi Kusmardi&lt;sup&gt;1&lt;/sup&gt;, Rahyussalim&lt;sup&gt;2&lt;/sup&gt;, Rizky Priambodo Wisnubaroto&lt;sup&gt;2,*&lt;/sup&gt;, Dilla Firzani&lt;sup&gt;3&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pathological Anatomy, Faculty of Medicine Indonesia, Universitas Indonesia, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Orthopaedic and Traumatology, Faculty of Medicine, Universitas Indonesia, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Undergraduate student Faculty of Medicine, Universitas Indonesia, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Swarna SK</style></author><author><style face="normal" font="default" size="100%">Nivedhitha MS</style></author><author><style face="normal" font="default" size="100%">Vishnu Priya V</style></author><author><style face="normal" font="default" size="100%">Gayathri R</style></author><author><style face="normal" font="default" size="100%">Selvaraj J</style></author><author><style face="normal" font="default" size="100%">Madhan K</style></author><author><style face="normal" font="default" size="100%">Shyamala Devi B</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Evaluation of Anti-Inflammatory Potential of Ethanolic Extract of Leaf, Bark and Flower of Tecoma stans with Ibuprofen- An In vitro Analysis</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory Effect</style></keyword><keyword><style  face="normal" font="default" size="100%">Bark</style></keyword><keyword><style  face="normal" font="default" size="100%">Flower</style></keyword><keyword><style  face="normal" font="default" size="100%">Leaf</style></keyword><keyword><style  face="normal" font="default" size="100%">Tecoma stans</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1088-1092</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Endodontics has always been indebted to pharmaceutical sciences to provide it with necessary analgesics and anti-inflammatory agents. More specifically, there has always been a need for anti-inflammatory phytotherapeutic agents as the commercially available synthetic anti inflammatory drugs have their own limitations due to undesirable side effects. Hence, novel potent analgesic and anti-inflammatory drugs without considerable side effects from the natural sources are under evaluation. &lt;em&gt;Tecoma stans&lt;/em&gt; (Bignoniaceae) is an ornamental plant found throughout India. It has been shown to have variety of medicinal properties. In the present study, we have shown that potential anti inflammatory activity of different parts of &lt;em&gt;Tecoma stans &lt;/em&gt;(&lt;em&gt;T.stants&lt;/em&gt;) and compared with standard drug. &lt;strong&gt;Aim: &lt;/strong&gt;To evaluate the &lt;em&gt;in vitro&lt;/em&gt; anti inflammatory potential of different parts of &lt;em&gt;T.stans&lt;/em&gt; ethanolic extract and to compare the anti inflammatory activity with standard drug ibuprofen. &lt;strong&gt;Methodology:&lt;/strong&gt; The ethanolic extraction of &lt;em&gt;T.stans’s&lt;/em&gt; bark, leaves and floweres was done as per the standard method. Different concentrations (100, 200, 300, 400 and 500 μg/ml) of the extracts were used for anti-inflammatory activity by inhibition of albumin denaturation. All samples were analyzed in triplicate. The results were statistically analyzed. &lt;strong&gt;Results: &lt;/strong&gt;All the three parts of the plant extract have shown to have anti inflammatory activity in a dose-dependent manner. However, the leaf and flower extracts of &lt;em&gt;T.stans&lt;/em&gt; were found to have 100 percent anti-inflammatory pontential than standard drug ibuprofen. &lt;strong&gt;Conclusion:&lt;/strong&gt; It is concluded from the present findings that T.stants possess anti-inflammatory properties which could be due to presence of active constitutents presen in the plant extracts. Hence,&lt;em&gt; T.stans&lt;/em&gt; may serve as one of the anti inflammatory herbal durgs for Endontic infection-induced inflammation and related to dental diseases. Further studies on the identification of the active principles present in the leaf and flower extract are warranted to assertatin its potentials.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1088</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Swarna SK&lt;sup&gt;1&lt;/sup&gt;, Nivedhitha MS&lt;sup&gt;1&lt;/sup&gt;, Vishnu Priya V&lt;sup&gt;2,&lt;/sup&gt;*, Gayathri R&lt;sup&gt;2&lt;/sup&gt;, Selvaraj J&lt;sup&gt;2&lt;/sup&gt;, Madhan K&lt;sup&gt;2&lt;/sup&gt;, Shyamala Devi B&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Conservative Dentistry &amp;amp; Endodontics, Saveetha Dental College &amp;amp; Hospitals, Saveetha Institute of Medical &amp;amp; Technical Sciences, Saveetha University, Chennai – 600 077, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biochemistry, Saveetha Dental College &amp;amp; Hospitals, Saveetha Institute of Medical &amp;amp; Technical Sciences, Saveetha University, Chennai – 600 077, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Nurrashida Binti Mok Hallim</style></author><author><style face="normal" font="default" size="100%">Aryo Tedjo</style></author><author><style face="normal" font="default" size="100%">Anwar Ibrahim</style></author><author><style face="normal" font="default" size="100%">Salinah</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparison between the Effect of Precipitate and Supernatant Aloe vera Gel on Experimental Cutaneous Wound Healing Using Optical Coherence Tomography</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Aloe vera</style></keyword><keyword><style  face="normal" font="default" size="100%">OCT</style></keyword><keyword><style  face="normal" font="default" size="100%">Precipitate</style></keyword><keyword><style  face="normal" font="default" size="100%">Supernatant</style></keyword><keyword><style  face="normal" font="default" size="100%">Wound Healing</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">405-412</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;!-- x-tinymce/html --&gt;&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Background:&lt;/strong&gt; Wound healing is a fundamental response to injured tissue that results in the restoration of tissue integrity. One of the famous herbs that promote wound healing is &lt;em&gt;Aloe vera&lt;/em&gt;. Despite well known for its therapeutic effect, several studies reported inconclusive evidence regarding this. Besides, lack of evidence to postulate the superior effect of two components of Aloe vera which are the precipitate and supernatant. &lt;strong&gt;Objective:&lt;/strong&gt; Study compares the effects of precipitate and supernatant in promoting tissue repair. Evaluation takes place by using optical Coherence Tomography (OCT) and is comparable with histopathology study. &lt;strong&gt;Methods:&lt;/strong&gt; Twelve male mice were randomly divided into four groups (precipitate, supernatant, control 50% ethanol, and normal). 200 mg of Aloe vera was extracted. A standardized 2 cm longitudinal incision wound was created. All mice were given topical &lt;em&gt;Aloe vera&lt;/em&gt;, 0.5 g each, once daily and assessment of wound surface was performed using OCT. The animals were sacrificed on day 10 to evaluate histopathologically. &lt;strong&gt;Results:&lt;/strong&gt; R parameter from the OCT was utilized to analyze the data. There is no significant difference in the treatment effect between &lt;em&gt;Aloe vera&lt;/em&gt; treated group and control on day 10 post-injury. Treated animals with precipitate did not differ significantly from supernatant treated group. Nevertheless, from histopathology analysis, precipitate showed better wound reepithelialisation, collagen formation and angionesis despite having numerous inflammatory cells. &lt;strong&gt;Conclusion:&lt;/strong&gt; OCT using R parameter is not the best choice to detect wound healing. Nevertheless, from histopathological perspective, Aloe vera accelerates wound healing and precipitate Aloe vera gel does have a superior effect from supernatant in promoting wound healing.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">405</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;!-- x-tinymce/html --&gt;&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Kusmardi Kusmardi&lt;sup&gt;1&lt;/sup&gt;, Nurrashida Binti Mok Hallim&lt;sup&gt;1&lt;/sup&gt;, Aryo Tedjo&lt;sup&gt;2&lt;/sup&gt;, Anwar Ibrahim&lt;sup&gt;3&lt;/sup&gt;, Salinah&lt;sup&gt;1,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Departement of Anatomical Pathology, Faculty of Medicine, Universitas, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Departement of Medicinal Chemistry, Faculty of Medicine, Universitas, INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Departement of Medicinal Physic, Faculty of Medicine, Universitas, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pharnuwan Chanhan</style></author><author><style face="normal" font="default" size="100%">Ampa Konsue</style></author><author><style face="normal" font="default" size="100%">Rachanee Nammatra</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Agricultural Model of using Fertilizer, Harvesting Time and Extraction Method on Phytochemical Contents and Antioxidant Activities from Mulberry Leaves Grown in Maha Sarakham Province, Thailand</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidation</style></keyword><keyword><style  face="normal" font="default" size="100%">Fertilizer</style></keyword><keyword><style  face="normal" font="default" size="100%">Harvesting</style></keyword><keyword><style  face="normal" font="default" size="100%">Mulberry leaves</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemistry</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">531-535</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Aims:&lt;/strong&gt; Phytochemical contents and free radical scavenging of Mulberry leaf extracts by using different fertilizer, time of harvesting and solvent extraction were evaluated. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Dried Mulberry leaves were extracted by using different solvent including aqueous, 50% ethanol and 95% ethanol. The phytochemical screening were determined by Total Phenolic Compounds (TPC) and Total Flavonoid Contents (TFC). The anti-oxidation were tested by using 2,2-diphenyl-1-picrylhydrazy (DPPH) radical scavenging and 2,2 -azinobis-(3- ethylbenzothiazoline-6-sulphonate) (ABTS&lt;sup&gt;+&lt;/sup&gt;) assay. &lt;strong&gt;Results: &lt;/strong&gt;This experimental study found that the mulberry leaf extract were given extraction with 95% ethanol, all of fertilizer and at Week 4 showed highest total phenolic contents espectcially BET2 was high amount of TPC (124.444±0.609 mgGE/gExt). The harvest time, all of groups at the Week 4 were significantly higher than all of groups at the Week 2. On the other hand, total flavonoid contents, the DET1 (Fertilizer formula 15-15-15, extraction with 95% ethanol at the Week 2; 110.913±3.208 mgQE/gExt) showed highest amount. The Antioxidant activities, DPPH free radical scavenging activity, The groups were given extraction with 95% ethanol, all of fertilizer at the Week 4 including CHT2 (IC&lt;sub&gt;50&lt;/sub&gt; =0.00459±0.00001 mg/mL), BHT2 (IC&lt;sub&gt;50&lt;/sub&gt; =0.00487 ±0.00005 mg/mL), AHT2 (IC&lt;sub&gt;50&lt;/sub&gt; =0.00499±0.00007 mg/mL), DHT2 (IC&lt;sub&gt;50&lt;/sub&gt; =0.00499±0.00005 mg/mL) and EHT2 (IC&lt;sub&gt;50&lt;/sub&gt; =0.00667 ±0.00039 mg/mL) were more potent on free radical scavenging higher than all of groups. The ABTS+ assay, at the Week 2 of all fertilizer groups were given with all solvent extraction including BHT1 (IC&lt;sub&gt;50&lt;/sub&gt; =0.03191±0.00257 mg/mL), CHT1 (IC&lt;sub&gt;50&lt;/sub&gt; =0.03247±0.00044 mg/mL), AHT1 (IC&lt;sub&gt;50&lt;/sub&gt; =0.03320±0.00120 mg/mL), EHT1 (IC&lt;sub&gt;50 &lt;/sub&gt;=0.03342±0.00116 mg/mL) and AAT1 (IC&lt;sub&gt;50&lt;/sub&gt; =0.03792±0.00076 mg/mL) showed free radical scavenging activity not different from standard substances, ascorbic acid (IC&lt;sub&gt;50&lt;/sub&gt; =0.00699 ±0.00004 mg/mL) and Trolox&lt;sup&gt;&lt;/sup&gt;&amp;nbsp;(IC&lt;sub&gt;50&lt;/sub&gt; =0.01594±0.00116 mg/mL).&lt;strong&gt; Conclusion:&lt;/strong&gt; The study was undertaken to investigate it’s fertilizer use, harvest time and extraction method for biologically activities also chemical composition contents and their antioxidant potentials. Therefore, our data might be help to good cultivation and harvesting practice selection in order to produce better of mulberry leaf production.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">531</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Pharnuwan Chanhan&lt;sup&gt;1&lt;/sup&gt;, Ampa Konsue&lt;sup&gt;2&lt;/sup&gt;, Rachanee Nammatra&lt;sup&gt;3,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Center of Excellence for Silk Innovation, Mahasarakham University, Maha Sarakham, 44150, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Medicine, Thai Traditional Medicine Research Unit, Mahasarakham University, Maha Sarakham, 44000, THAILAND.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Production and Quantity Control of Herbal Tea Laboratory, Biodiversity and Conservation Research Unit, Walai Rukhavej Botanical Research Institute, Mahasarakham University, Maha Sarakham, 44150, THAILAND.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dwisari Dillasamola</style></author><author><style face="normal" font="default" size="100%">Yufri Aldi</style></author><author><style face="normal" font="default" size="100%">Marselani Kolobinti</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Coriander Ethanol Extract (Coriandrum sativum L.) Against Phagocytosis Activity and Capacity of the Macrophage Cells and the Percentage of Leukocyte Cells in White Male Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Coriandrum sativum</style></keyword><keyword><style  face="normal" font="default" size="100%">Leukocytes</style></keyword><keyword><style  face="normal" font="default" size="100%">Macrophages</style></keyword><keyword><style  face="normal" font="default" size="100%">Phagocytosis capacity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1290-1298</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Coriander has long been used by humans as a traditional drug and to enhances the taste of foods. This study aims to know the effects of coriander ethanol extract against phagocytosis activity and capacity of the macrophage cells and the percentage of leukocytes. The test animals used were white male mice which divided into 4 groups and each group consists of 5 mice. The first group (control) was given with 0.5% Na CMC suspension. The second, the third, and the fourth groups were given with coriander extract each with doses of 100 mg/kg, 140 mg/kg and 200 mg/kg orally for 7 days long. On the 8th day, the mice were induced by &lt;em&gt;Staphylococcus aureus &lt;/em&gt;to help their immune system. The results showed that the administration of coriander extract at doses of 100, 140 and 200 mg/kg can increase the phagocytic activity of macrophages by 44.6%; 54.2%; and 60.2% each, while the phagocytic capacity replaces the results of 95.8; 104.4; and 126 cells. The total number of leukocytes showed were 5210, 6190, and 7310 /μL blood. In the number of leukocyte cells, the amount of coriander extract can reduce the number of neutrophil and monocyte cell segments. The conclusion of this study regarding coriander ethanol extract at doses of 100, 140 and 200 mg/kg can increase phagocytosis activity and capacity of the macrophage cells and the total leukocyte cell counts in male white mice.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1290</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Dwisari Dillasamola*, Yufri Aldi, Marselani Kolobinti&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Faculty of Pharmacy, Department of Pharmacology, Andalas University, Padang, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rezi Riadhi Syahdi</style></author><author><style face="normal" font="default" size="100%">Aditya Sindu Sakti</style></author><author><style face="normal" font="default" size="100%">Agung Kristiyanto</style></author><author><style face="normal" font="default" size="100%">Riky Redmawati</style></author><author><style face="normal" font="default" size="100%">Abdul Mun’im</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Gamma Irradiation on Some Pharmacological Properties and Microbial Activities of Melinjo (Gnetum gnemon Linn.) Seeds</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Dipeptidyl peptidase-4</style></keyword><keyword><style  face="normal" font="default" size="100%">Gamma irradiation</style></keyword><keyword><style  face="normal" font="default" size="100%">Gnetum gnemon</style></keyword><keyword><style  face="normal" font="default" size="100%">HMG-CoA reductase</style></keyword><keyword><style  face="normal" font="default" size="100%">Resveratrol</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">177-182</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Background:&lt;/strong&gt; Ionizing radiation, such as gamma irradiation, serves as a useful approach to inhibit spore germination and to control pathogens in postharvest seeds. Recently, its application on phytochemical sources and its influence on antioxidant activity of various phytochemical compounds has become an interesting topic to be explored.&lt;strong&gt; Objective:&lt;/strong&gt; The objectives of this study were to determine the effect of gamma irradiation as sterilization method on the resveratrol content and its antioxidant, HMG-CoA reductase inhibitory and dipeptidyl peptidase-4 (DPP-4) inhibitory activities of Melinjo (&lt;em&gt;Gnetum gnemon&lt;/em&gt;) seeds. &lt;strong&gt;Methods:&lt;/strong&gt; In this research, melinjo seeds were irradiated by 0.0; 2.5; 5.0; 7.5; and 10.0 kGy with gamma irradiation and then extracted with ethanol. The extracts were tested for resveratrol content with HPLC, antioxidant activities by DPPH assay, HMG-CoA inhibitory activity using HMG-CoA reductase assay kit and DPP-4 inhibitory activity using DPP-4 Inhibitor Screening Assay Kit. Gamma irradiation has effect on resveratrol content, antioxidant activity, HMG-CoA reductase inhibition and DPP-4 inhibitory activity. &lt;strong&gt;Results:&lt;/strong&gt; From the research, the highest value of resveratrol content is 0.18±0.004 mg/g seeds powder found in 5.0 kGy gamma irradiation treatment with IC50 94.64±0.236 μg/mL, while the highest HMG-CoA reductase inhibition is shown in 2.5 kGy irradiation dose. Melinjo seeds irradiated by 2.5 kGy gamma irradiation also shown a significant increase of DPP-4 inhibition activity. &lt;strong&gt;Conclusion:&lt;/strong&gt; This study suggests that 2.5-5 kGy radiation is the effective gamma irradiation dose to improve the quality of melinjo seeds.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">177</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Rezi Riadhi Syahdi&lt;sup&gt;1&lt;/sup&gt;, Aditya Sindu Sakti&lt;sup&gt;2&lt;/sup&gt;, Agung Kristiyanto&lt;sup&gt;2&lt;/sup&gt;, Riky Redmawati&lt;sup&gt;2&lt;/sup&gt;, Abdul Mun’im&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Departement of Medicinal Chemistry, Analysis and Biomedics Laboratory, Faculty of Pharmacy, Universitas INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Drug Development Laboratory, Faculty of Pharmacy, Universitas INDONESIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Departement of Pharmacognosy-Phytochemistry, Universitas INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yufri Aldi</style></author><author><style face="normal" font="default" size="100%">Hasanatul Khairiyah</style></author><author><style face="normal" font="default" size="100%">Nila Kasuma</style></author><author><style face="normal" font="default" size="100%">Afriwardi</style></author><author><style face="normal" font="default" size="100%">Agus Sri Banowo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Noni Fruit Extract (Morinda citrifolia L.) in Gingivitis Patient</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chlorhexidine</style></keyword><keyword><style  face="normal" font="default" size="100%">Gingival index</style></keyword><keyword><style  face="normal" font="default" size="100%">Morinda citrifolia L.</style></keyword><keyword><style  face="normal" font="default" size="100%">Mouthwash</style></keyword><keyword><style  face="normal" font="default" size="100%">Noni fruit extract</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">678-682</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Antiseptic mouthwash (chlorhexidine and povidone iodine) is usually used to decrease the number of colonies of pathogenic bacteria. But, somehow it gives side effect if it used for a long time. So, it should take another alternative as a raw material to make a mouthwash with minimal side effects, economical and efficacious. &lt;strong&gt;Aim: &lt;/strong&gt;The aim of this research was to examine the effect of noni fruit extract (&lt;em&gt;Morinda citrifolia &lt;/em&gt;L.) that given as mouthwash on 15 gingivitis patients.&lt;strong&gt; Materials and Methods: &lt;/strong&gt;The research was conducted for 7 days in a row and gingival index of each patient was measured before and after the treatment. The patients were divided into 3 group and given 3 different treatments. Group I used mouthwash noni fruit extract 5%; Group II used chlorhexidine 0.1%; and Group III used a mixture of extracts of noni: chlorhexidine (2.5% : 0.05%). The mouthwash was used in the morning and at the night before going to sleep as much as 15 ml and gargling it for 30 sec. &lt;strong&gt;Results: &lt;/strong&gt;The results showed the gingival index was declined in every group treatment (mouthwash noni fruit extract 5%, chlorhexidine 0.1% and a mixture of extracts of noni: chlorhexidine (2.5% : 0.05%). The differences between each group were not significant (&lt;em&gt;p&lt;/em&gt; &amp;gt; 0.05).&lt;strong&gt; Conclusion:&lt;/strong&gt; Despite it give the same effect, the extract of noni fruit should be used as an alternative to mouthwash because it gives the same effect as much as chlorhexidine and it also economical, efficacious and minimal side effects.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">678</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Yufri Aldi&lt;sup&gt;1,*&lt;/sup&gt;, Hasanatul Khairiyah&lt;sup&gt;1&lt;/sup&gt;, Nila Kasuma&lt;sup&gt;2&lt;/sup&gt;, Afriwardi&lt;sup&gt;3&lt;/sup&gt;, Agus Sri Banowo&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Faculty of Pharmacy, Universitas Andalas, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Departement Oral Biology, Faculty of Dentistry, Universitas Andalas, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department Physiology Medicine, Faculty of Medicine, Universitas Andalas, Padang, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department Mental Health and Community Nursing, Faculty of Nursing, Universitas Andalas, Padang, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">T Sundarrajan</style></author><author><style face="normal" font="default" size="100%">V Velmurugan</style></author><author><style face="normal" font="default" size="100%">MK Kathiravan</style></author><author><style face="normal" font="default" size="100%">K Manikandan</style></author><author><style face="normal" font="default" size="100%">KS Lakshmi</style></author><author><style face="normal" font="default" size="100%">MR Ganesh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Effect of Ultraviolet-B Radiation Exposure on Hibiscus cannabinus Linn with its Phytochemical and Pharmacological Responses</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cancer cells line HT-29</style></keyword><keyword><style  face="normal" font="default" size="100%">Hibiscus cannabinus Linn</style></keyword><keyword><style  face="normal" font="default" size="100%">Total Phenolic Contents</style></keyword><keyword><style  face="normal" font="default" size="100%">UV-B radiation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1540-1543</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Aim: &lt;/strong&gt;Exposure of UV-B Radiation on&amp;nbsp;&lt;em&gt;Hibiscus cannabinus&lt;/em&gt; Linn and to evaluate both Phytochemical and Pharmacological responses. &lt;strong&gt;Objective:&lt;/strong&gt; UV-B can increase the nutrients contents from plants, plants become tastier and increases the yield and UV-will make plants resistant to fungal infections and stimulate the production of phytomarkers. &lt;strong&gt;Material and Methods: &lt;/strong&gt;&lt;em&gt;Hibiscus cannabinus&lt;/em&gt; Linn seeds were soaked with 50% H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; for 12 hours and then inoculated with the Azospirillum. UV-B radiation cabinet was provided by UV lamps which are above 15 cm from control maintained. Normal daylight exposed control group Seedlings irradiated for 2 hour per day (12.30 pm to 2.30 pm) for 20 days. &lt;strong&gt;Results and Discussion: &lt;/strong&gt;20 days treatment increases total phenolic contents and sugars content were decreased in uncovered leaf tissue. Protein content was at first diminished but expanded on the 20 day of UV-B treatment. Also, perform pharmacological studies no toxic elements are observed 20 days treatment and pharmacological activity by using anticancer activity by using human colon HT-29 cancer cell line. UV light exposed plants shows good anticancer activity when compared with non UV exposed Plant.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1540</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;T Sundarrajan&lt;sup&gt;1,&lt;/sup&gt;*, V Velmurugan&lt;sup&gt;1&lt;/sup&gt;, MK Kathiravan&lt;sup&gt;2&lt;/sup&gt;, K Manikandan&lt;sup&gt;3&lt;/sup&gt;, KS Lakshmi&lt;sup&gt;3&lt;/sup&gt;, MR Ganesh&lt;sup&gt;4&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Chemistry SRM College of Pharmacy, SRMIST, Kattankulathur, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;209, Dr. APJ Abdul Kalam Research Lab SRM College of Pharmacy, SRMIST, Kattankulathur, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmaceutical Analysis, SRM College of Pharmacy, SRMIST, Kattankulathur, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;IIISM, SRM IST, Kattankulathur, Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Eka Sunarwidhi Prasedya</style></author><author><style face="normal" font="default" size="100%">Ni Wayan Riyani Martyasari</style></author><author><style face="normal" font="default" size="100%">Candra Dwipayana Hamdin</style></author><author><style face="normal" font="default" size="100%">Masao Miyake</style></author><author><style face="normal" font="default" size="100%">Daisuke Kobayashi</style></author><author><style face="normal" font="default" size="100%">Sri Widyastuti</style></author><author><style face="normal" font="default" size="100%">Akihiro Hazama</style></author><author><style face="normal" font="default" size="100%">Haji Sunarpi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effectiveness of Methanol Solvent Extraction for Red Macroalgae Acanthophora spicifera Antitumoric Activity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acanthophora</style></keyword><keyword><style  face="normal" font="default" size="100%">Antiproliferative</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Indonesia</style></keyword><keyword><style  face="normal" font="default" size="100%">Macroalgae</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">450-454</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Red macroalgae &lt;em&gt;Acanthophora spicifera&lt;/em&gt; is commonly found in most parts of Indonesia coastal areas. However, information regarding their potential pharmaceutical uses remains largely unexplored. This study evaluates the antiproliferative activity of &lt;em&gt;Acanthophora spicifera&lt;/em&gt; collected from Indonesian extracted with different solvents of ethanol and methanol. &lt;strong&gt;Methods:&lt;/strong&gt; Cytotoxicity and antiproliferative activity of &lt;em&gt;A. spicifera&lt;/em&gt; crude ethanol extract (AS-EtOH) and &lt;em&gt;A. spicifera&lt;/em&gt; crude methanol extract (AM-MetOH) were evaluated with Lactate dehidrogenase (LDH) and Trypan blue exclusion assay in Human cervical cancer (HeLa) cells for 72h. Concentration of extracts treated in HeLa cells were 6.25 to 200 &lt;em&gt;μ&lt;/em&gt;g/mL. Viability staining with fluorescence stain Hoechst33342/PI was conducted to investigate apoptotic activity. Potential apoptotic activity of treatments was confirmed by DNA fragmentation assay. &lt;strong&gt;Results:&lt;/strong&gt; AS-MetOH demonstrated high cytotoxicity in HeLa cells with IC&lt;sub&gt;50&lt;/sub&gt; of 127.3 ± 33.13 &lt;em&gt;μ&lt;/em&gt;g/mL. However, AS-EtOH IC&lt;sub&gt;50&lt;/sub&gt; values could not be determined in this study. Antiproliferative activity was highly significant in AS-MetOH treated cells as cell density was suppressed to 20 x 10&lt;sup&gt;4&lt;/sup&gt; cells/mL compared to AS-EtOH (73 x 10&lt;sup&gt;4&lt;/sup&gt; cells/mL) and untreated cells (83 x 10&lt;sup&gt;4&lt;/sup&gt; cells/mL). Finally, apoptotic activity could be determined in AS-MetOH treated cells with increase PI fluorescence emitting cells and DNA fragmentation. On the other hand, apoptotic activity was not observable in AS-EtOH treated cells based on fluorescence viability staining and DNA fragmentation assay. &lt;strong&gt;Conclusion:&lt;/strong&gt; Current results show methanol solvent as an effective solvent to promote potential pharmaceutical properties of macroalgae &lt;em&gt;A. spicifera. &lt;/em&gt;Further advanced studies in a compound level from&lt;em&gt; A. spicifera&lt;/em&gt; methanol fraction would be reasonable for development of macroalgae based anticancer agent.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">450</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Eka Sunarwidhi Prasedya&lt;sup&gt;1&lt;/sup&gt;, Ni Wayan Riyani Martyasari&lt;sup&gt;2&lt;/sup&gt;, Candra Dwipayana Hamdin&lt;sup&gt;2&lt;/sup&gt;, Masao Miyake&lt;sup&gt;4&lt;/sup&gt;, Daisuke Kobayashi&lt;sup&gt;4&lt;/sup&gt;, Sri Widyastuti&lt;sup&gt;3&lt;/sup&gt;, Akihiro Hazama&lt;sup&gt;4&lt;/sup&gt;, Haji Sunarpi&lt;sup&gt;1,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Bioscience and Biotechnology Research Centre, Faculty of Mathematics and Natural Sciences, University of Mataram, Nusa Tenggara Bar- 83126, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacy, Medical Faculty, University of Mataram, Nusa Tenggara Bar-83126 INDONSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Food Science and Agroindustrial Technology, University of Mataram, Nusa Tenggara Bar-83126 INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Cellular and Integrative Physiology, Fukushima Medical University, Fukushima, JAPAN.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vinodini NA</style></author><author><style face="normal" font="default" size="100%">Pratik Kumar Chatterjee</style></author><author><style face="normal" font="default" size="100%">Kunal</style></author><author><style face="normal" font="default" size="100%">Suman VB</style></author><author><style face="normal" font="default" size="100%">Rashmi KS</style></author><author><style face="normal" font="default" size="100%">Nayanatara AK</style></author><author><style face="normal" font="default" size="100%">Anupama N</style></author><author><style face="normal" font="default" size="100%">Ramesh M. Bhat</style></author><author><style face="normal" font="default" size="100%">Sheela Joice P</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effectiveness of Moringa oleifea Extract in Attenuating the Toxic Effect on Platelet Count: An Experiment on Cadmium Exposed Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cadmium</style></keyword><keyword><style  face="normal" font="default" size="100%">Clotting Mechanisms</style></keyword><keyword><style  face="normal" font="default" size="100%">Moringa oleifera</style></keyword><keyword><style  face="normal" font="default" size="100%">Platelet Count</style></keyword><keyword><style  face="normal" font="default" size="100%">Toxicity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">689-693</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Aims and Objective:&lt;/strong&gt; To determine the role of &lt;em&gt;Moringa oleifera&lt;/em&gt; on total platelet count alterations (T-PC) in rats treated with cadmium. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;In the present study female adult Wistar Albino rats, (180-200) gm were divided into, Group I-normal control, Group II-pretreated control, group III-cadmium treated , group IV- pre-treated with &lt;em&gt;Moringa oleifera &lt;/em&gt;leaf extract (MOE) and then administered oral cadmium for a day, with &lt;em&gt;n&lt;/em&gt;=6 each &lt;strong&gt;Results: &lt;/strong&gt;Indicate that the pre-treatment with MOE (100 mg/kg/bw) prior to cadmium infusion augmented the level of total platelet count (&lt;em&gt;p&lt;/em&gt;≤0.001) as compared to the cadmium-exposed group, which might have a role in clotting mechanisms also. &lt;strong&gt;Conclusion: &lt;/strong&gt;&lt;em&gt;Moringa oleifera &lt;/em&gt;extract has a beneficial effect on platelet count in cadmium-induced animal model.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">689</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Vinodini NA&lt;sup&gt;1&lt;/sup&gt;, Pratik Kumar Chatterjee&lt;sup&gt;1,*&lt;/sup&gt;, Kunal&lt;sup&gt;1&lt;/sup&gt;, Suman VB&lt;sup&gt;1&lt;/sup&gt;, Rashmi KS&lt;sup&gt;1&lt;/sup&gt;, Nayanatara AK&lt;sup&gt;1&lt;/sup&gt;, Anupama N&lt;sup&gt;1&lt;/sup&gt;, Ramesh M. Bhat&lt;sup&gt;1&lt;/sup&gt;, Sheela Joice P&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Physiology, Kasturba Medical College, Mangalore, Manipal Academy of Higher Education (MAHE), Manipal, Karnataka, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Physiology, MES Medical College, Perinthalmanna, Kerala, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nitin Govindrao Dumore</style></author><author><style face="normal" font="default" size="100%">Milind Janrao Umekar</style></author><author><style face="normal" font="default" size="100%">Brijesh Gulabrao Taksande</style></author><author><style face="normal" font="default" size="100%">Manish Manohar Aglawe</style></author><author><style face="normal" font="default" size="100%">Nandkishor Ramdasji Kotagale</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of Withania somnifera Nicotine Induced Conditioned Place Preference in Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Condition place preference</style></keyword><keyword><style  face="normal" font="default" size="100%">Nicotine</style></keyword><keyword><style  face="normal" font="default" size="100%">Withania somnifera</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">43-47</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Background:&lt;/strong&gt; Herbal medicines can be novel treatment strategies for management of nicotine addiction. Withania somnifera (Ashwagandha) is an Indian medicinal plant of great medicinal value; used in many clinically proven conditions. Objective: In present study we aimed at investigating the effect of withania somnifera extract (WSE) on preventing nicotine mediated effects attributed for the development of addiction. &lt;strong&gt;Material and Methods:&lt;/strong&gt; Mice were treated with nicotine and/or WSE and subjected to nicotine induced conditioned place preference (CPP) in male albino mice was checked.&lt;strong&gt; Results: &lt;/strong&gt;Application of two-way ANOVA showed that with preconditioning and post-conditioning values as a within-subjects (column) factor and treatment as an independent between subject (row) factor. Two-way ANOVA revealed significant effect of treatment [F(3,40)=4.119, p&amp;lt;0.05], time [F(1,40)=23.76, p&amp;lt;0.001] and interactiontreatment x time [F(3,40)=5.244, p&amp;lt;0.01] on Intra-peritoneal (ip) administration of nicotine (1 mg/kg). WSE did not produce any changes in the preference to drug-paired compartment. Factors like treatment [F(3,40) = 0.656, p&amp;gt;0.05], time [F(1,40) = 7.383, p&amp;lt;0.01] and interactiontreatment x time [F(3,40) = 0.5748, p&amp;gt;0.05] showed insignificant effects. Withania somnifera (50,100,200 mg/kg ip) coadministered with nicotine during the 6 days conditioning sessions completely abolished the acquisition of nicotine-induced CPP in mice. &lt;strong&gt;Conclusion:&lt;/strong&gt; Above data indicate that withania somnifera attenuate nicotine induced CPP. Hence it has potential as an anti-addictive therapy.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">43</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Nitin Govindrao Dumore&lt;sup&gt;1,2*&lt;/sup&gt;, Milind Janrao Umekar&lt;sup&gt;1&lt;/sup&gt;, Brijesh GulabraoTaksande&lt;sup&gt;1&lt;/sup&gt;, Manish Manohar Aglawe&lt;sup&gt;1&lt;/sup&gt;, Nandkishor Ramdasji Kotagale&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Neuroscience, Department of Pharmacology, Smt.kishoritai Bhoyar College of pharmacy Kamptee, Nagpur 441002 Maharashtra, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Dadasaheb Balpande College of Pharmacy, Besa, Nagpur,440037 Maharashtra, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacognosy, Government college of Pharmacy, Amaravati, 444601, Maharashtra, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kishor Mazumder</style></author><author><style face="normal" font="default" size="100%">Ziku Chandra Dey</style></author><author><style face="normal" font="default" size="100%">Suparna Dey</style></author><author><style face="normal" font="default" size="100%">Md. Fazlul Kabir</style></author><author><style face="normal" font="default" size="100%">Minhazur Rahman</style></author><author><style face="normal" font="default" size="100%">Sadiur Rahman Sajon</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Anti-diarrheal and Anti-nociceptive Activity of Methanolic Unripe Fruit Peels Extract of Masua ferrea Linn. on Mice Models</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-diarrheal</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-nociceptive</style></keyword><keyword><style  face="normal" font="default" size="100%">Castor oil</style></keyword><keyword><style  face="normal" font="default" size="100%">Intestinal transit</style></keyword><keyword><style  face="normal" font="default" size="100%">Mesua ferrea</style></keyword><keyword><style  face="normal" font="default" size="100%">Tail immersion method</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">828-835</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Though traditionally the plant &lt;em&gt;Masua ferrea &lt;/em&gt;has been used by south east Asian people in inflammation and septic conditions, the present study was designed to investigate the anti-diarrheal and anti-nociceptive activities of unripe fruit peel of &lt;em&gt;Mesua ferrea&lt;/em&gt; on animal models. &lt;strong&gt;Methods:&lt;/strong&gt; Various methods were employed for investigating these activities such as castor-oil induced diarrhea, castor-oil induced enteropooling and gastrointestinal motility test, acetic acid induced writhing test, tail immersion and hot plate methods. &lt;strong&gt;Results: &lt;/strong&gt;From the experimental data it was found that the diarrheal episode was inhibited by 39.68% and 49.21% for methanol extract at the doses of 100 and 200 mg/kg respectively. The extract significantly lessened the intestinal volume for methanolic extract at 200 mg/Kg dose 0.54 ± 0.01 ml (&lt;em&gt;p &lt;/em&gt;&amp;lt; 0.05) and at 200 mg/Kg dose 0.47 ± 0.02 ml (&lt;em&gt;p&lt;/em&gt; &amp;lt; 0.01) compared to control 0.65 ± 0.03 ml in castor-oil induced enteropooling and also decreased intestinal transit 29.07 – 48.54% for methanolic extract comparable with standard (loperamide 5 mg/kg). &lt;em&gt;Mesua ferrea&lt;/em&gt; peels significantly (&lt;em&gt;P&lt;/em&gt; &amp;lt; 0.05, &lt;em&gt;P&lt;/em&gt; &amp;lt; 0.01 and &lt;em&gt;P&lt;/em&gt; &amp;lt; 0.001) reduced the number of writhing, increased latency to flick tail in tail immersion method and elevated the mean basal reaction time in hot plate method respectively. Besides, no delayed toxicity was observed in given doses. &lt;strong&gt;Conclusion:&lt;/strong&gt; The methanolic extract exhibited highly significant anti-diarrheal and antinociceptive activity in a dose-dependent manner, which supports its use in traditional herbal medicine.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">828</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Kishor Mazumder&lt;sup&gt;1,3,*&lt;/sup&gt;, Ziku Chandra Dey&lt;sup&gt;2&lt;/sup&gt;, Suparna Dey&lt;sup&gt;4&lt;/sup&gt;, Md. Fazlul Kabir&lt;sup&gt;2&lt;/sup&gt;, Minhazur Rahman&lt;sup&gt;2&lt;/sup&gt;, Saidur Rahaman sajon&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacy, Jessore University of Science and Technology, Jessore-7408, Jessore, BANGLADESH.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;University of Science and Technology Chittagong (USTC), Chittagong, BANGLADESH.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;School of Biomedical Sciences and Graham Centre for Agricultural Innovation, Charles Sturt University, Boorooma St, Wagga Wagga, NSW, AUSTRALIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Center for Specialized Care and Research, Chittagong-4000, BANGLADESH.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lubna F. Abu-Niaaj</style></author><author><style face="normal" font="default" size="100%">Ibrahim Katampe</style></author><author><style face="normal" font="default" size="100%">Shtaywy S. Abdalla</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Antispasmodic Effect of Arcapillin on Smooth Muscles of Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antispasmodic</style></keyword><keyword><style  face="normal" font="default" size="100%">Arcapillin</style></keyword><keyword><style  face="normal" font="default" size="100%">Artemisia monosperma</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavone</style></keyword><keyword><style  face="normal" font="default" size="100%">Smooth Muscles</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">712-717</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Arcapillin, 2',4',5-trihydroxy-5',6,7–trimethoxyflavone, is a flavone aglycone isolated from several &lt;em&gt;Artemisia&lt;/em&gt; species, though, it was first identified from &lt;em&gt;A. capillaris&lt;/em&gt;. The &lt;em&gt;Artemisia&lt;/em&gt; species are used in folk medicine as a remedy for gastrointestinal and liver illnesses, hypertension, fever and inflammation. Studies indicated a potential role of arcapillin to relieve symptoms of liver disorders; however, there is no report yet in the literature of its effect on smooth muscles. &lt;strong&gt;Objective:&lt;/strong&gt; Our study aims to evaluate the effect of arcapillin, isolated from &lt;em&gt;A. monosperma&lt;/em&gt;, on the contractile activity of rat smooth muscles. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Increased concentrations of arcapillin were tested on isolated rat ileum, pulmonary artery, trachea, and urinary bladder. The muscle contraction was recorded upon addition of arcapillin in eight cumulative concentrations of half log units in the range of [10&lt;sup&gt;-7&lt;/sup&gt; M -3×10&lt;sup&gt;-4 &lt;/sup&gt;M]. Depending on the organ-containing muscles, the preparations were treated with arcapillin either at basal tonus or after pre-stimulated via a contractile agent; 10&lt;sup&gt;-3&lt;/sup&gt; M O-acetylcholine on ileum and 10&lt;sup&gt;-5&lt;/sup&gt; M L-phenylephrine on pulmonary artery rings. Control tissues were treated with sodium hydroxide in an equivalent concentration to that used to dissolve the flavone. &lt;strong&gt;Results:&lt;/strong&gt; Arcapillin caused a dose-dependent relaxation on ileum preparation and pulmonary artery. The inhibition of the contractile activity of ileum was reversible within 60 seconds after washing off the flavone. The urinary bladder showed a slight increase in contraction at the highest concentrations starting at [10&lt;sup&gt;-4 &lt;/sup&gt;M] of arcapillin. There was no observed effect on the contraction of tracheal smooth muscles by all tested concentrations of arcapillin. &lt;strong&gt;Conclusion:&lt;/strong&gt; The antispasmodic activity of arcapillin may contribute to the pharmaceutical importance of &lt;em&gt;A. monosperma &lt;/em&gt;in particularly to treat gastrointestinal disorders.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">712</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Lubna F. Abu-Niaaj&lt;sup&gt;1,*&lt;/sup&gt;, Ibrahim Katampe&lt;sup&gt;1&lt;/sup&gt;, Shtaywy S. Abdalla&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Agricultural and Life Sciences, Central State University, Wilberforce, OH 45384, USA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biological Sciences, University of Jordan, Amman, JORDAN.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Puneshwar Keshari</style></author><author><style face="normal" font="default" size="100%">Pradeep</style></author><author><style face="normal" font="default" size="100%">Sudhakar Bhat</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Hepatoprotective Potential of Rhododendron arboreum Sm. Stem Bark as Abhava Pratinidhi Dravya (Substitute) of Rohitaka (Tecomella undulata (Sm.) Seem.) Against Paracetamol Induced Hepatotoxicity in Experimental Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Abhava Pratinidhi Dravya</style></keyword><keyword><style  face="normal" font="default" size="100%">Choorna</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatoprotective</style></keyword><keyword><style  face="normal" font="default" size="100%">Kwatha</style></keyword><keyword><style  face="normal" font="default" size="100%">Rhododendron arboreum</style></keyword><keyword><style  face="normal" font="default" size="100%">Rohitaka</style></keyword><keyword><style  face="normal" font="default" size="100%">Substitute</style></keyword><keyword><style  face="normal" font="default" size="100%">Tecomella undulata</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1148-1154</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Rohitaka (&lt;em&gt;Tecomella undulata&lt;/em&gt; (Sm.) Seem.) has been considered as threatened and listed as rare at international level (IUCN, 2000). In Ayurveda classics, Rohitaka is described as Yakritpleehgulmodarhara (useful in liver and spleenic disorders). &lt;em&gt;Rhododendron arboreum&lt;/em&gt; Sm. is used by folklore practitioners for treatment of Jaundice and marketed as Rohitaka in Nepal. &lt;strong&gt;Aim: &lt;/strong&gt;To evaluate &lt;em&gt;Rhododendron arboreum&lt;/em&gt; Sm. as an effective pratinidhi dravya (substitute) in abhava (absence) of Rohitaka (&lt;em&gt;Tecomella undulata&lt;/em&gt; (Sm.) Seem.) with special reference to hepatoprotective activity in paracetamol induced hepatotoxicity in rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; In the present study, hepatoprotective effect of Choorna (powder) and Kwatha (decoction) of &lt;em&gt;Rhododendron arboreum&lt;/em&gt; Sm. and &lt;em&gt;Tecomella undulata&lt;/em&gt; (Sm.) Seem. (Choorna-0.54 g/kg body wt. and Kwatha- 4.32 ml/kg body wt. p. o. for 10 days along with paracetamol toxicant 3 g/kg body wt. p. o. on 6&lt;sup&gt;th&lt;/sup&gt; and 8&lt;sup&gt;th &lt;/sup&gt;day) were investigated against paracetamol induced hepatotoxicity. Silymarin (100 mg/kg body wt.) was used as standard hepatoprotective reference drug. &lt;strong&gt;Statistical Analysis Used:&lt;/strong&gt; The obtained data were analyzed by ANOVA with Dunnet's multiple ‘t’ test and level of p&amp;lt;0.05 was considered as statistically significant. &lt;strong&gt;Results: &lt;/strong&gt;Paracetamol treatment led to elevated levels of liver marker enzymes and disorientation in histological observations which were significantly reversed by treatment with &lt;em&gt;Rhododendron arboreum&lt;/em&gt; Sm. and &lt;em&gt;Tecomella undulata&lt;/em&gt; (Sm.) Seem. dependent on dosage forms. &lt;strong&gt;Conclusion: &lt;/strong&gt;The study revealed that both the drugs have similar hepatoprotective effect and thus &lt;em&gt;Rhododendron arboreum&lt;/em&gt; Sm. as “Abhava Pratinidhi Dravya” for &lt;em&gt;Tecomella undulata&lt;/em&gt; (Sm.) Seem. with special reference to hepatoprotective activity is justified.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1148</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Puneshwar Keshari*, Pradeep, Sudhakar Bhat &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Department of Dravyaguna, SDM College of Ayurveda and Hospital, Hassan- 573201, Karnataka, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">D.Sivaraman</style></author><author><style face="normal" font="default" size="100%">N.Anbu</style></author><author><style face="normal" font="default" size="100%">N.Kabilan</style></author><author><style face="normal" font="default" size="100%">M.Pitchiah Kumar</style></author><author><style face="normal" font="default" size="100%">P.Shanmugapriya</style></author><author><style face="normal" font="default" size="100%">G.J.Christian</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Exploration of Anti-Urolithiasis Potential of Traditional Siddha Formulations Amukkara Chooranam and Karisalai Karpam Chooranam by Struvite Crystal Growth Inhibition Assay</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Amukkara Chooranam</style></keyword><keyword><style  face="normal" font="default" size="100%">Crystals</style></keyword><keyword><style  face="normal" font="default" size="100%">Karisalai karpam chooranam</style></keyword><keyword><style  face="normal" font="default" size="100%">Lithotripsy</style></keyword><keyword><style  face="normal" font="default" size="100%">Polyherbal</style></keyword><keyword><style  face="normal" font="default" size="100%">Traditional medicines</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">683-688</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;Urolithiasis is a medical condition characterized by formation of stone which comprises of calcium oxalate, magnesium ammonium phosphate and uric acid. Reoccurrence becomes the primary hindering factor in providing relief for urolithiasis; hence there is a need of alternate therapeutic strategy that may effectively combat and halt the formation and nucleation of the crystals. &lt;strong&gt;Objective: &lt;/strong&gt;The main aim of the present investigation is to explore the anti-urolithiasis potential of the two versatile siddha formulations Amukkara Chooranam (AKC) and Karisalai Karpam Chooranam (KKC) using diffusion gel growth technique. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Silica hydrogel matrix was divided in to three groups which were control, AKC and KKC treated groups. Test drugs were screened at two dose levels of 0.5% and 1%. The efficiency of the formulations was screened by comparing the crystal size of the control and treatment medium. &lt;strong&gt;Results: &lt;/strong&gt;The average size of the crystals in the control medium was found to be 2.12 ± 0.22 cm, whereas the crystal size was significantly decreased in medium contains 0.5% and 1% of AKC with the size of 1.4 ± 0.15 and 1.14 ± 0.18 cm. Similar type of findings were observed in medium consist of 0.5% and 1 % KKC with the size of 1.52 ± 0.13 and 1.08 ± 0.17 cm. &lt;strong&gt;Conclusion: &lt;/strong&gt;Results clearly indicates that both the siddha formulations offers maximum percentage inhibition on the crystal growth in the tested medium, this efficacy may be due to presence of versatile phytocomponents present in the formulations.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">683</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;D.Sivaraman&lt;sup&gt;1,&lt;/sup&gt;*, N.Anbu&lt;sup&gt;2&lt;/sup&gt;, N.Kabilan&lt;sup&gt;3&lt;/sup&gt;, M.Pitchiah Kumar&lt;sup&gt;4&lt;/sup&gt;, P.Shanmugapriya&lt;sup&gt;5&lt;/sup&gt;, G.J.Christian&lt;sup&gt;6&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Centre for Laboratory Animal Technology and Research, Col.Dr.Jeppiaar Research Park, Sathyabama Institute of Science and Technology , Jeppiaar Nagar, Rajiv Gandhi road, Chennai – 600 119,Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pothu Maruthuvam, Govt. Siddha Medical College, Chennai-600106, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Siddha, The Tamil Nadu Dr.M.G.R. Medical University, Chennai - 600032, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;State Drug Licensing Authority (Indian System of Medicine), Arumbakkam, Chennai – 600106, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Nanjunoolum Maruthuva Neethi Noolum, National Institute of Siddha, Tambaram Sanatorium, Chennai-47, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Noi Naadal, National Institute of Siddha, Tambaram Sanatorium, Chennai-47, Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Boualem HARFI</style></author><author><style face="normal" font="default" size="100%">Lakhdar KHELIFI</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hairy Root Technology: Effect of Etiolation on Datura sp. Transgenic Root Induction and Hyoscyamine Production</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Datura sp.</style></keyword><keyword><style  face="normal" font="default" size="100%">Etiolation</style></keyword><keyword><style  face="normal" font="default" size="100%">Gas chromatography</style></keyword><keyword><style  face="normal" font="default" size="100%">Hairy roots</style></keyword><keyword><style  face="normal" font="default" size="100%">Hyoscyamine</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">991-995</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Hyoscyamine, because of its medicinal properties, is an important tropane alkaloid. In order to implement a biotechnological process for its production, hairy roots of&lt;em&gt; Datura &lt;/em&gt;species resulting from genetic transformation by &lt;em&gt;Agrobacterium rhizogenes&lt;/em&gt; A4 strain have been the subject of this work. In the &lt;em&gt;in vitro &lt;/em&gt;alkaloids production programs, optimization of the transformation is a crucial step for obtaining a large number of root lines allowing the selection of efficient lines. &lt;strong&gt;Methods:&lt;/strong&gt; The conditions for hairy roots induction were explored by studying the effect of &lt;em&gt;Datura&lt;/em&gt; sp. &lt;em&gt;in vitro&lt;/em&gt; seedling etiolation on the genetic transformation. The first step was the establishment of &lt;em&gt;Datura&lt;/em&gt; &lt;em&gt;in vitro&lt;/em&gt; plantlet cultures followed by the hairy roots induction with A4 strain of &lt;em&gt;A. rhizogenes&lt;/em&gt;. The confirmation of the genetic transformation was performed by polymerase chain reaction (PCR) analysis of rolB gene in the roots. After hyoscyamine extraction, it was analyzed (quantitatively and qualitatively) by gas chromatography. Results: 343 root lines were obtained in total, 96 root lines from non-etiolated &lt;em&gt;Datura in vitro&lt;/em&gt; seedlings and 247 root lines from etiolated &lt;em&gt;in vitro&lt;/em&gt; plantlets. After the selection of six transgenic root lines, tow root lines from each species (&lt;em&gt;D. tramonium, D. tatula &lt;/em&gt;and&lt;em&gt; D. innoxia&lt;/em&gt;), one from non-etiolated &lt;em&gt;in vitro &lt;/em&gt;plantlet and one from etiolated &lt;em&gt;in vitro&lt;/em&gt; plantlet, the most hyoscyamine content was 8.43 mg/g D.W. obtained with &lt;em&gt;D. tatula&lt;/em&gt; etiolated &lt;em&gt;in vitro&lt;/em&gt; seedling. &lt;strong&gt;Conclusion: &lt;/strong&gt;The etiolated&lt;em&gt; in vitro&lt;/em&gt; plantlets seem more favorable to hairy roots induction.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">991</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Boualem HARFI&lt;sup&gt;1,2,&lt;/sup&gt;*, Lakhdar KHELIFI&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Biotechnology Research Center (C.R.Bt), Constantine, ALGERIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;National Higher School of Agronomy (ENSA – El-Harrach), Algiers, ALGERIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gan B Bajracharya</style></author><author><style face="normal" font="default" size="100%">Pratigya KC</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A High Antibacterial Efficacy of Fruits of Litsea cubeba (Lour.) Pers from Nepal. GC-MS and Antioxidative Capacity Analyses</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Brine-shrimp assay</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH assay</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Litsea oil</style></keyword><keyword><style  face="normal" font="default" size="100%">Minimum bactericidal concentration</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">889-893</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Biological activities of the plant materials may vary with different geographic origin. &lt;em&gt;Litsea cubeba &lt;/em&gt;fruits are consumed in Nepal as a spice ingredient and are considered to be possessed antibacterial property. &lt;strong&gt;Objectives:&lt;/strong&gt; Aims of this work are: to compare phytoconstituents present in litsea oil by GC-MS analysis, and to evaluate antibacterial and antioxidant activities of the volatile oil and the fruit extracts. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Hydrodistillation of &lt;em&gt;L. cubeba&lt;/em&gt; fruits was performed to obtain litsea oil followed by extractions with boiling methanol. Fractionations of the extract provided hexane, dichloromethane, ethyl acetate and aqueous extracts. The oil and extracts were analysed for the phytochemicals present. They were evaluated by using antibacterial susceptibility, brine-shrimp lethality and antioxidant capacity assays. &lt;strong&gt;Results:&lt;/strong&gt; All together 49 compounds (accounting 93.66%) were identified in the litsea oil by GC-MS. Monoterpenes being dominant components, the oil constituted 15.96% of citral (geranial and neral). Other major constituents were capric acid (12.44%), β-caryophyllene oxide (7.69%), linalool (5.96%), eucalyptol (5.13%) and cis- β-terpineol (4.22%). Litsea oil, hexane extract and dichloromethane extract displayed very effective antibacterial property. Ethyl acetate extract (LC&lt;sub&gt;50&lt;/sub&gt; = 21.52 μg mL‒1) and litsea oil (LC&lt;sub&gt;50&lt;/sub&gt; = 31.62 μg mL‒1) were found highly cytotoxic against brine-shrimp nauplii. Ethyl acetate (IC&lt;sub&gt;50&lt;/sub&gt; = 124.57 μg mL‒1) and dichloromethane (IC&lt;sub&gt;50&lt;/sub&gt; = 271.08 μg mL‒1) extracts displayed a modest DPPH free radical scavenging activity. &lt;strong&gt;Conclusion:&lt;/strong&gt; Phytoconstituents present in the &lt;em&gt;L. cubeba&lt;/em&gt; fruits from Nepal were analysed. Litsea oil and the extracts have displayed high antibacterial and potentially anticarcinogenic activities.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">889</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Gan B Bajracharya&lt;sup&gt;1,&lt;/sup&gt;*, Pratigya KC&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Science, Nepal Academy of Science and Technology (NAST), Khumaltar, Lalitpur, NEPAL.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemistry, Tri-Chandra Multiple Campus, Tribhuvan University, Kathmandu, NEPAL.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Emmanuel Kofi Kumatia</style></author><author><style face="normal" font="default" size="100%">Stephen Antwi</style></author><author><style face="normal" font="default" size="100%">Henry Brew-Daniels</style></author><author><style face="normal" font="default" size="100%">Alfred Ampoma Appiah</style></author><author><style face="normal" font="default" size="100%">Augustine Ocloo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In vivo Comparative Anti-Inflammatory and Analgesic Activities of Root Bark, Stem and Leaf Extracts of Capparis erythrocarpus (Capparaceae)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hot plate</style></keyword><keyword><style  face="normal" font="default" size="100%">Oedema</style></keyword><keyword><style  face="normal" font="default" size="100%">Pain</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical constituents</style></keyword><keyword><style  face="normal" font="default" size="100%">Writhing assay</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">515-520</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;The root bark powder of the medicinal plant &lt;em&gt;Capparis erythrocarpus &lt;/em&gt;is used at the Centre for Plant Medicine Research (In Ghana) against inflammatory pain disorders. The whole plant is destroyed to obtain the root bark which constitutes only 11.1 % of the plant. Hence, the plant is going extinct. We therefore sought to evaluate anti-inflammatory and analgesic activities of the root bark, stem and leaf of &lt;em&gt;C. erythrocarpus&lt;/em&gt; in order to explore them as substitute(s) anti-inflammatory and analgesic agent to the root bark. &lt;strong&gt;Methods:&lt;/strong&gt; Carrageenan induced paw oedema assay was used to evaluate anti-inflammatory activity. Hot plate and acetic acid induced writhing assays were employed to ascertain analgesic activity. &lt;strong&gt;Results:&lt;/strong&gt; The extracts of the root bark (CRB) and leaf (CL) produced significant (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05) antiinflammatory activity of 48.93 and 37.42 % at 50 and 200 mg/kg p.o. respectively whereas the stem extract (CS) was inactive. Moreover, the extracts produced significant (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05) analgesic activity. The analgesic activity (178.20 – 248.70 %) of the extracts were higher than that of morphine (136.70%) at 5 mg/kg i.m. in the hot plate assay. CS (200 mg/kg p.o.) produced the highest analgesic activity (54.61%) among the extracts and diclofenac sodium (41.15%) at 5 mg/kg p.o. in the writhing assay. &lt;strong&gt;Conclusion:&lt;/strong&gt; These results indicates that the leaf of &lt;em&gt;C. erythrocarpus &lt;/em&gt;can be substituted for the root as analgesic and anti-inflammatory agent. Whiles, the stem can also be used as analgesic agent. This will save the plant from extinction.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">515</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Emmanuel Kofi Kumatia&lt;sup&gt;1,*&lt;/sup&gt;, Stephen Antwi&lt;sup&gt;2&lt;/sup&gt;, Henry Brew-Daniels&lt;sup&gt;1&lt;/sup&gt;, Alfred Ampomah Appiah&lt;sup&gt;1&lt;/sup&gt;, Augustine Ocloo&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Phytochemistry, Centre for Plant Medicine Research, Mampong-Akwapim, GHANA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology, Centre for Plant Medicine Research, Mampong-Akwapim, GHANA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">KM Meselhy</style></author><author><style face="normal" font="default" size="100%">Ghada A Abdel-latif</style></author><author><style face="normal" font="default" size="100%">Amany A sleem</style></author><author><style face="normal" font="default" size="100%">Walaa Ayman</style></author><author><style face="normal" font="default" size="100%">Maram K Imam</style></author><author><style face="normal" font="default" size="100%">Kholoud A Kassab</style></author><author><style face="normal" font="default" size="100%">Sherouk Eissa</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of Milk on Phenolic Composition and Antioxidant Power of Black Tea</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Black tea</style></keyword><keyword><style  face="normal" font="default" size="100%">Glutathione</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC. Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Milk</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolics</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">October 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1262-1268</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Tea leaves are rich in several polyphenolics and flavonoidal compounds that could potentially have health-promoting properties. The objective of the present study was to analyze the antioxidant capacity of black tea and to study the effect of addition of fresh milk and packed milk on the phenolics concentrations and antioxidant efficacy. &lt;strong&gt;Methods:&lt;/strong&gt; The black tea infusion (BT), black tea infusion with fresh milk (BTFM) &amp;amp; black tea infusion with packed milk (BTPM) samples were comparatively analyzed for total phenolics, flavonoids and HPLC profiling of major phenolic content. All samples were investigated for their total antioxidant capacity and glutathione level in different organs (brain, liver, kidney and heart). &lt;strong&gt;Results:&lt;/strong&gt; The results shown that BT(black tea infusion) had higher total phenolics and flavonoids followed by BTPM (black tea infusion with packed milk) and then the BTFM (black tea infusion with fresh milk). The analytical HPLC results obtained also indicated that BT contained higher amount of catechins and garlic acid derivatives than BTFM, and BTPM may be due to chelation of free phenolics with some fats and protein in the tested milk samples, which reduces the levels of free phenolics significantly. Concerning antioxidants capacity both tested milk samples reduced antioxidant capacity to more than 50% in different tested tissues. &lt;strong&gt;Conclusion: &lt;/strong&gt;We conclude that black tea is a valuable source of antioxidants and that the inhibitory effect of milk on the total antioxidant capacity may be related to complex formation of the fat &amp;amp; protein content of the milk with major phenolics in the black tea.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1262</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;KM Meselhy&lt;sup&gt;1&lt;/sup&gt;,*, Ghada A Abdel-latif&lt;sup&gt;2&lt;/sup&gt;, Amany A sleem&lt;sup&gt;3&lt;/sup&gt;, Walaa Ayman&lt;sup&gt;4&lt;/sup&gt;, Maram.K.Imam&lt;sup&gt;4&lt;/sup&gt;, Kholoud A Kassab&lt;sup&gt;4&lt;/sup&gt;, Sherouk Eissa&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Pharmacognosy Department, Faculty of Pharmacy, Cairo University, EGYPT.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacology and Toxicology Department, Faculty of Pharmacy, Misr International University, EGYPT.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Pharmacology Department, National Research Center, Giza, EGYPT.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Fresh graduates, research center, Faculty of Pharmacy, Misr International University, EGYPT.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lakshmanan G</style></author><author><style face="normal" font="default" size="100%">Sivaraj C</style></author><author><style face="normal" font="default" size="100%">Ammar A</style></author><author><style face="normal" font="default" size="100%">Anantha Krishnan D</style></author><author><style face="normal" font="default" size="100%">Gopinath S</style></author><author><style face="normal" font="default" size="100%">Saravanan K</style></author><author><style face="normal" font="default" size="100%">Gunasekaran K</style></author><author><style face="normal" font="default" size="100%">Murugesan K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Isolation and Structural Elucidation of Allantoin a Bioactive Compound from Cleome viscosa L.: A Combined Experimental and Computational Investigation</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Allantoin</style></keyword><keyword><style  face="normal" font="default" size="100%">Antibacterial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Cleome viscosa</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword><keyword><style  face="normal" font="default" size="100%">XRD</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1391-1400</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Allantoin, a crystalline compound was isolated from the methanolic extract of &lt;em&gt;Cleome viscosa &lt;/em&gt;and it was reported for first time from this plant. The structure of Allantoin was elucidated by single crystal XRD and it was further confirmed through FTIR and ESI-MS spectroscopy techniques. It was crystallized in monoclinic crystal system with the space group P2i/c. Electronic structure characterization of the isolated Allantoin was done through density functional theory calculation. The atomic charges, dipole moment, frontier molecular orbital and the electrostatic potential map of the molecule in the gaseous phase and in the active site have also been analyzed. The optimized geometry was used for molecular docking to identify the possible binding mode. Furthermore, the &lt;em&gt;in vitro &lt;/em&gt;antibacterial activity of the isolated Allantoin against Gram-positive and Gram-negative bacteria was evaluated. Maximum Inhibitory Concentrations (MIC) of isolated Allantoin results showed 4 μg/mL for &lt;em&gt;B. subtilis&lt;/em&gt; and 8 μg/mL for &lt;em&gt;S. aureus, E. coli and K. pneumoniae.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1391</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Lakshmanan G&lt;sup&gt;1&lt;/sup&gt;, Sivaraj C&lt;sup&gt;2&lt;/sup&gt;, Ammar A&lt;sup&gt;3,&lt;/sup&gt;*, Anantha Krishnan D&lt;sup&gt;4&lt;/sup&gt;, Gopinath S&lt;sup&gt;5&lt;/sup&gt;, Saravanan K&lt;sup&gt;6&lt;/sup&gt;, Gunasekaran K&lt;sup&gt;4&lt;/sup&gt;, Murugesan K&lt;sup&gt;7&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;CAS in Botany, University of Madras, Guindy Campus, Chennai – 600025, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;ARMATS Biotek Training and Research Institute, Guindy, Chennai – 600032, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Food science department, College of Agriculture, University of Basrah, 61004, IRAQ.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;CAS in Crystallography and Biophysics, University of Madras, Guindy Campus, Chennai – 600025, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Physics, RKM Vivekananda College (Autonomous), Mylapore, Chennai – 600004, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Physics, Periyar University, Salem – 636011, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;7&lt;/sup&gt;SRM – Institute of Science &amp;amp; Technology, Ramapuram Campus, Chennai – 600089, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nartunai Govindarajan</style></author><author><style face="normal" font="default" size="100%">Susikumar Sundharamoorthy</style></author><author><style face="normal" font="default" size="100%">Narayanan Kannan</style></author><author><style face="normal" font="default" size="100%">Ilavarasan Raju</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Macro-Microscopic Identification of Dried Flowers of Hibiscus rosa-sinensis L. and its Differentiation from Adulterant Rhododendron arboreum Sm.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adulteration</style></keyword><keyword><style  face="normal" font="default" size="100%">Hibiscus rosa-sinensis</style></keyword><keyword><style  face="normal" font="default" size="100%">Macro-microscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">Rhododendron arboreum</style></keyword><keyword><style  face="normal" font="default" size="100%">Semparathai</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">613-616</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Hibiscus rosa-sinensis&lt;/em&gt; Linn. (Fam.Malvaceae) is a small evergreen shrub cultivated in gardens throughout India. The decoction of flowers is used in Indian system of Medicine for bronchial inflammation, urinary astringent and cardio tonic, to promote growth and to prevent graying of hair. The dried flowers of &lt;em&gt;Rhododendron arboreum&lt;/em&gt; Sm. (Fam.Ericaceae) are morphologically looking similar to &lt;em&gt;Hibiscus rosa-sinensis&lt;/em&gt; and used as adulterant in the market. Hence, the morphological, Micro-morphological and powder microscopical studies on dried flowers of &lt;em&gt;Hibiscus rosa-sinensis&lt;/em&gt; and &lt;em&gt;Rhododendron arboreum &lt;/em&gt;was carried out and reported. &lt;strong&gt;Objective: &lt;/strong&gt;To identify the dried flowers of Hisbiscus rosa-sinensis macro-microscopically and to differentiate it from adulterant &lt;em&gt;Rhododendron arboreum&lt;/em&gt;. &lt;strong&gt;Methods:&lt;/strong&gt; The morphology and powder microscopy were observed following standard methods and photographed. &lt;strong&gt;Results: &lt;/strong&gt;The colour, taste, arrangement and appearance of calyx, corolla and stamen, trichomes, calcium oxalate crystals, sclereids, oil globules and pollen grains are found to be differentiating diagnostic characters in raw drug/powdered form of dried flowers of &lt;em&gt;Hibiscus rosa-sinensis&lt;/em&gt; and &lt;em&gt;Rhododendron arboreum&lt;/em&gt;. &lt;strong&gt;Conclusion:&lt;/strong&gt; The finding of present study is helpful in standardization of formulation consists of &lt;em&gt;Hibiscus rosa-sinensis &lt;/em&gt;as ingredient in their powdered form and also for authentication/identification of dried flowers of&lt;em&gt; Hibiscus rosa-sinensis&lt;/em&gt;.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Short Communication</style></work-type><section><style face="normal" font="default" size="100%">613</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Nartunai Govindarajan&lt;sup&gt;1,*&lt;/sup&gt;, Susikumar Sundharamoorthy&lt;sup&gt;2&lt;/sup&gt;, Narayanan Kannan&lt;sup&gt;3&lt;/sup&gt;, Ilavarasan Raju&lt;sup&gt;4&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Research Officer, Department of Pharmacognosy, Captain Srinivasa Murthy Regional Ayurveda Drug Development Institute, CCRAS, Govt. of India, Chennai – 600 106, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Research Scholar, Captain Srinivasa Murthy Regional Ayurveda Drug Development Institute, CCRAS, Govt. of India, Chennai – 600 106, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Laboratory Technician, Captain Srinivasa Murthy Regional Ayurveda Drug Development Institute, CCRAS, Govt. of India, Chennai – 600 106, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Assistant Director, Captain Srinivasa Murthy Regional Ayurveda Drug Development Institute, CCRAS, Govt. of India, Chennai – 600 106, Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mansi Chitkara</style></author><author><style face="normal" font="default" size="100%">Rajneet Kohli</style></author><author><style face="normal" font="default" size="100%">Inderjeet Singh Sandhu</style></author><author><style face="normal" font="default" size="100%">Didar Singh</style></author><author><style face="normal" font="default" size="100%">Gagandeep Kaur</style></author><author><style face="normal" font="default" size="100%">Rakesh Kumar Sindhu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mineral Content Analysis of Polyherbal Energy Bar Using X-Ray Fluorescence Technique</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Calcium</style></keyword><keyword><style  face="normal" font="default" size="100%">Energy bar</style></keyword><keyword><style  face="normal" font="default" size="100%">Iron</style></keyword><keyword><style  face="normal" font="default" size="100%">Mineral content</style></keyword><keyword><style  face="normal" font="default" size="100%">Polyherbal</style></keyword><keyword><style  face="normal" font="default" size="100%">Potassium</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">53-56</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Aim:&lt;/strong&gt; The objective of the present study was to develop a novel energy bar which is nutritious and cost effective. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The components used for the novel energy bar were banana, orange, peanuts, raisins, cocoa butter, stevia leaves and oats. Mineral contents of energy bar were analysed by XRF technique. &lt;strong&gt;Results:&lt;/strong&gt; The mineral contents were present in comparable amount. Major elements viz. K 17.15%, P 4.57%, Mg 1.43%, Ca 0.93%, Na 0.66%, S 0.54%, Fe 0.15%, Zn 0.05% and Cu 0.02% were present in energy bar. &lt;strong&gt;Conclusion:&lt;/strong&gt; Minerals are good for overall growth of body. The energy bar also contains no preservatives, binding agents and sugar free. So, the energy bar is major source of energy and minerals for all age group individuals.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">53</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Mansi Chitkara&lt;sup&gt;1&lt;/sup&gt;, Rajneet Kohli&lt;sup&gt;2&lt;/sup&gt;, Inderjeet Singh Sandhu&lt;sup&gt;1&lt;/sup&gt;, Didar Singh&lt;sup&gt;2&lt;/sup&gt;, Gagandeep Kaur&lt;sup&gt;3&lt;/sup&gt;, Rakesh Kumar Sindhu&lt;sup&gt;3* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Nanomaterials Research Laboratory, Department of Applied Sciences, Chitkara University, Rajpura, Patiala – 140401, Punjab, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Chitkara College of Hotel Management and Catering, Chitkara University, Rajpura, Patiala –140401, Punjab, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacognosy and Natural Products, Chitkara College of Pharmacy, Chitkara University, Rajpura, Patiala – 140401, Punjab, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vivek Jagadeesan Sharavanan</style></author><author><style face="normal" font="default" size="100%">Muthusaravanan Sivaramakrishnan</style></author><author><style face="normal" font="default" size="100%">Ram Kothandan</style></author><author><style face="normal" font="default" size="100%">Shanmugaprakash Muthusamy</style></author><author><style face="normal" font="default" size="100%">Kumaravel Kandaswamy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular Docking Studies of Phytochemicals from Leucas aspera Targeting Escherichia coli and Bacillus subtilis Subcellular Proteins</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimicrobials</style></keyword><keyword><style  face="normal" font="default" size="100%">Computational screening</style></keyword><keyword><style  face="normal" font="default" size="100%">Docking</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword><keyword><style  face="normal" font="default" size="100%">Subcellular proteins</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">278-285</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;!-- x-tinymce/html --&gt;&lt;strong&gt;Objective:&lt;/strong&gt; Bacterial subcellular proteins play a vital role in cell division, pilus assembly and virulence. In addition, such proteins were perceived as potential antimicrobial targets. Therefore, in this article we attempt to screen for potential phytochemicals that can target those subcellular proteins. &lt;strong&gt;Methods:&lt;/strong&gt; A computational screening for phytochemicals from Leucas aspera with better bioavailability followed by molecular docking studies for better understanding of interaction between phytochemical and target proteins. &lt;strong&gt;Results:&lt;/strong&gt; erythro-2-(4-allyl-2,6- dimethoxyphenoxy)-1-(4-hydroxy-3-methoxyphenyl) propan-1-ol and Leucasperone B from Leucas aspera possess great binding affinity (&amp;gt; -100 kcal/mol) towards one or more bacterial subcellular protein targets and possess bioavailability. &lt;strong&gt;Conclusion:&lt;/strong&gt; Based on the docking result we claim that erythro-2-(4-allyl-2,6-dimethoxyphenoxy)-1-(4-hydroxy-3-methoxyphenyl) propan-1-ol and Leucasperone B could serve as an effective antimicrobial compounds to treat bacterial infections.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">278</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;!-- x-tinymce/html --&gt;&lt;!-- x-tinymce/html --&gt;&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Vivek Jagadeesan Sharavanan, Muthusaravanan Sivaramakrishnan, Ram Kothandan, Shanmugaprakash Muthusamy, Kumaravel Kandaswamy*&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&amp;nbsp;Department of Biotechnology, Laboratory of Molecular Biology and Genetic Engineering, Kumaraguru College of Technology, Coimbatore, Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Digvijay Verma</style></author><author><style face="normal" font="default" size="100%">Shilpi Singh</style></author><author><style face="normal" font="default" size="100%">Renu Arya</style></author><author><style face="normal" font="default" size="100%">Soundararajan Rajan</style></author><author><style face="normal" font="default" size="100%">Bhopal Singh Arya</style></author><author><style face="normal" font="default" size="100%">Anil Khurana</style></author><author><style face="normal" font="default" size="100%">Raj Kumar Manchanda</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Morpho-anatomical Observations on Homoeopathic Plant Drug Hygrophila spinosa T. Anderson</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Drug</style></keyword><keyword><style  face="normal" font="default" size="100%">Homoeopathy</style></keyword><keyword><style  face="normal" font="default" size="100%">Macroscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">microscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">Organoleptic</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">286-291</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Hygrophila auriculata&lt;/em&gt; (Schumach.) Heine synonym &lt;em&gt;Hygrophila spinosa&lt;/em&gt; T. Anderson is used in the homoeopathic system of medicine belongs to the family Acanthaceae. Plant contains terpenoids, alkaloids, flavonoids and is traditionally known as an aphrodisiac, renal tonic and for its health-promoting properties, this drug is most popularly used by homoeopathic practitioners for the treatment of urticaria, conjunctivitis, gastroenteritis, nausea etc. Complete morphological characterization of whole plant has not been reported so for. This study may provide complete information on the basis of morphological, anatomical and powdered studies. That will assist to differentiate between adulterants and authentic raw drug to maintain the quality of drugs. &lt;strong&gt;Objective:&lt;/strong&gt; The aim of the present study is to examine the morpho-anatomical, powder and fluorescence analysis of whole plant i.e. root, stem, and leaf of the plant used in homoeopathy.&lt;strong&gt; Material and methods:&lt;/strong&gt; The macroscopical, microscopical and powdered analysis of drug was performed. For morphological study simple observational methods applied while for anatomical and bio-statistical parameters microscopy including powder microscopy was performed by using different methods. &lt;strong&gt;Results:&lt;/strong&gt; The drug was in form of dried pieces of leaves, small quadrangular pieces of stem with spines and roots. Microscopy showed few features like aerenchymatous cortex in the middle region of root; semi-quadrangular outline, four vascular bundles at each corner in young stem and developing fascicular vascular bundles between them, in mature stem 6 vascular bundles viz. 4 vascular bundles at corner and 2 vascular bundles present in between opposite to each other; broad cortical aerenchyma in mature stem, leaf amphistomatous, anomocytic stomata, crescent-shaped meristele in leaf. &lt;strong&gt;Conclusion:&lt;/strong&gt; Present study can assist the diagnostic characters of &lt;em&gt;Hygrophila spinosa&lt;/em&gt; may be taken as pharmacognostical standards for the identification of plant drug.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">286</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Digvijay Verma&lt;sup&gt;1,*&lt;/sup&gt;, Shilpi Singh&lt;sup&gt;1&lt;/sup&gt;, Renu Arya&lt;sup&gt;3&lt;/sup&gt;, Soundararajan Rajan&lt;sup&gt;2&lt;/sup&gt;, Bhopal Singh Arya&lt;sup&gt;1&lt;/sup&gt;, Anil Khurana&lt;sup&gt;3&lt;/sup&gt;, Raj Kumar Manchanda&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Pharmacognosy Division, Drug Standardization Unit, Dr. D. P. Rastogi Central Research Institute for Homoeopathy, A-1/1, Sector 24 Noida, Uttar Pradesh-201301, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Medicinal Plant Garden Unit, Center for Medicinal Plants Research in Homoeopathy, 3/126 Indira Nagar Emerald, Tamil Nadu- 643209, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Drug Standardization Unit, Central Council for Research in Homoeopathy, D Block, Janakpuri, New Delhi- 110058, INDIA..&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nguyen Van Long</style></author><author><style face="normal" font="default" size="100%">Chu Van Men</style></author><author><style face="normal" font="default" size="100%">Anh Vu Tuan</style></author><author><style face="normal" font="default" size="100%">Nguyen Van Manh</style></author><author><style face="normal" font="default" size="100%">Thanh Chu Duc</style></author><author><style face="normal" font="default" size="100%">Ha Bui Thi Thu</style></author><author><style face="normal" font="default" size="100%">Hoang Van Luong</style></author><author><style face="normal" font="default" size="100%">Le Bach Quang</style></author><author><style face="normal" font="default" size="100%">Pham Gia Khanh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A New LC/MS/MS Method for the Analysis of Phyllanthin in Rat Plasma and its Application on Comparative Bioavailability of Phyllanthin in Different Formulations after Oral Administration in Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">LC-MS/MS</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacokinetics</style></keyword><keyword><style  face="normal" font="default" size="100%">Phospholipid</style></keyword><keyword><style  face="normal" font="default" size="100%">Phyllanthin</style></keyword><keyword><style  face="normal" font="default" size="100%">Plasma</style></keyword><keyword><style  face="normal" font="default" size="100%">Quantitation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">968-975</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;A simple, short UPLC/MS/MS method for quantitation of phyllanthin in rat plasma in less than 2 minutes have been developed and fully validated. The validated method was used to investigate the pharmacokinetic properties of phyllanthin in PA extract and phospholipid complex of PA extract in rat. &lt;strong&gt;Methods:&lt;/strong&gt; The separation was carried out on Acquity C&lt;sub&gt;18 &lt;/sub&gt;(50 x 2.1 mm; 1.7 μm), with a mobile phase of 10 mM aqueous amonium acetate and acetonitrile (10:90; v/v), at a flow rate of 0.2 mL/min. Felodipin was used as internal standard. Phyllanthin is extracted from a small volume of rat plasma (100 μl) by means of liquid-liquid extraction method with tert butyl methyl ether. Electrospray ionization (ESI) mass spectrometry was applied in positive mode at capillary voltage of 4000 V for both phyllanthin and IS, cone voltage of 24 V for phyllanthin and 20 V for IS, desolvation temperature of 360oC, cone gas flow of 25 L/h, collision energy of 12 V for phyllanthin and 10 V for IS. Multiple reaction monitoring (MRM) was used to monitor the transitions at m/z (Q1/Q3) 436.41/355.36 for phyllanthin and 384.20/352.18 for IS. &lt;strong&gt;Results:&lt;/strong&gt; The linear calibration curve of phyllanthin was obtained over the concentration range of 0.5 – 100 ng/mL. The intra‐ and inter‐day precisions were less than 7.08 % and the accuracies were within ± 7.55%. The Cmax values of phyllanthin from two different preparations in rat plasma after oral administration of 2.0 mg/kg were 11.44 and 31.44 ng/ml, and the AUC values were 18.07 and 41.43 h.ng/ml, respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; A simple, short UPLC/MS/MS method for quantitation of phyllanthin in rat plasma in less than 2 minutes have been developed and fully validated. The bioavailability of phyllanthin from the phospholipid complex of PA extract in rat plasma was significantly improved compared with that of raw PA extract after oral administration.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">968</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Nguyen Van Long&lt;sup&gt;#&lt;/sup&gt;, Chu Van Men&lt;sup&gt;#,&lt;/sup&gt;*, Anh Vu Tuan, Nguyen Van Manh, Thanh Chu Duc, Ha Bui Thi Thu, Hoang Van Luong, Le Bach Quang, Pham Gia Khanh&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;nstitute of Biomedicine and Pharmacy, Vietnam Military Medical University, 222-Phung Hung Street, Ha Dong District, Hanoi, VIETNAM.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;#&lt;/sup&gt;These authors contributed equally to this work&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Srinivasa Naidu Parijatham Kanchana</style></author><author><style face="normal" font="default" size="100%">Agnel Arul John Nayagam</style></author><author><style face="normal" font="default" size="100%">Sandra Horta</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic Profile of Root and Stem of Indigofera Tirunelvelica Sanjappa</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alkaloid</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoid</style></keyword><keyword><style  face="normal" font="default" size="100%">Indigofera tirunelvelica Sanjappa</style></keyword><keyword><style  face="normal" font="default" size="100%">Root</style></keyword><keyword><style  face="normal" font="default" size="100%">Stem</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1580-1586</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;The focus on herbal plants as medicine is increasing rapidly because of their efficacy and less side effects. The medicinal plants are great alternative as they are renewable and non exhaustive resources. In India these medicinal plants have been part of the people’s life dating back from centuries. &lt;strong&gt;Objectives:&lt;/strong&gt; The present study is aimed to evaluate anatomical characterization of stem and root of &lt;em&gt;Indigofera tirunelvelica&lt;/em&gt; Sanjappa for the first time which can be used in the identification and standardisation of &lt;em&gt;Indigofera tirunelvelica&lt;/em&gt; Sanjappa. &lt;strong&gt;Results: &lt;/strong&gt;The stem and root of the plant were evaluated for their microscopic features. In that histochemical localisation of secondary metabolites and transverse section of stem and root were studied. The histochemical localisation result reveals the presence of terpenoids, alkaloids, flavonoids and lignin were found in epidermal, cortical and xylem regions of the stem. Alkaloids, Terpenoids, phenols and lignin were found in the different areas of root. &lt;strong&gt;Conclusion: &lt;/strong&gt;The present study thus emphasis the potentiality of the plant as a drug.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1580</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Srinivasa Naidu Parijatham Kanchana&lt;sup&gt;1&lt;/sup&gt;, Agnel Arul John Nayagam&lt;sup&gt;2,&lt;/sup&gt;*, Sandra Horta&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biochemistry, St, Francis College for Women (Autonomous), Hyderabad, Telangana, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;PG and research Department of Biochemistry, Srimad Andavan Arts and Science College (Autonomous), Tiruchirappalli, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Assistant Professor, Department of Biochemistry, St, Francis College for Women (Autonomous), Hyderabad, Telangana, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Twumasi Mary A</style></author><author><style face="normal" font="default" size="100%">Ekuadzi Edmund</style></author><author><style face="normal" font="default" size="100%">Mante Priscilla K</style></author><author><style face="normal" font="default" size="100%">Boakye-Gyasi Mariam E</style></author><author><style face="normal" font="default" size="100%">Mensah Merlin LK</style></author><author><style face="normal" font="default" size="100%">Woode Eric</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic Studies of the Leaves, Stem and Root of Capparis erythrocarpos Isert (Capparaceae)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Capers</style></keyword><keyword><style  face="normal" font="default" size="100%">Cicatrices</style></keyword><keyword><style  face="normal" font="default" size="100%">crystal sheaths</style></keyword><keyword><style  face="normal" font="default" size="100%">Herbal medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Morphological features</style></keyword><keyword><style  face="normal" font="default" size="100%">Physicochemical parameters</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">112-118</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The roots of &lt;em&gt;Capparis erythrocarpos&lt;/em&gt; are used traditionally across Africa for the management of pain, arthritis and other forms of inflammatory conditions. Owing to its proven efficacy, it has gained commercial value, particularly as a key ingredient in several herbal products and alcoholic beverages. The increased scarcity owing to demand outstripping supply lend the roots of &lt;em&gt;C. erythrocarpos&lt;/em&gt; to adulteration. This paper presents a detailed pharmacognostic evaluation of the leaf, stem and root of &lt;em&gt;C. erythrocarpos&lt;/em&gt; which will be used in its identification and consequent standardization. &lt;strong&gt;Methods:&lt;/strong&gt; The leaf, stem and root were evaluated for their macroscopic and microscopic features as were the physicochemical parameters and phytochemical screening done. &lt;strong&gt;Results:&lt;/strong&gt; Leaves are alternately arranged, have collateral vascular bundle, crystal sheaths and a pericyclic fibre. Actinocytic stomata and secretory cells were contained in powdered leaves. The stem showed lenticels and thorns, stellate and branched trichomes which leave off cicatrices in older stems. The powdered stem and roots contained stone cells, secretory cells and scalariform vessels. However, the roots lacked thorns, trichomes and had smaller secretory cells. Aqueous and ethanolic extracts of the leaves, stem and roots were slightly acidic to neutral. Ash values of leaves, stem and roots are (16.58 ± 0.09) % w/w, (5.01 ± 0.09) % w/w and (6.53 ± 0.19) % w/w respectively. Preliminary phytochemical screening of the leaves, stem and roots showed the presence of glycosides, flavonoids and tannins. &lt;strong&gt;Conclusion:&lt;/strong&gt; The determined parameters for the leaf, stem and root of &lt;em&gt;C. erythrocarpos&lt;/em&gt; constitute quality parameters for their unequivocal identification.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">112</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Twumasi Mary A&lt;sup&gt;1&lt;/sup&gt;, Ekuadzi Edmund&lt;sup&gt;1,*&lt;/sup&gt;, Mante Priscilla K&lt;sup&gt;2&lt;/sup&gt;, Boakye-Gyasi Mariam E&lt;sup&gt;3&lt;/sup&gt;, Mensah Merlin LK&lt;sup&gt;4&lt;/sup&gt;, Woode Eric&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Faculty of Pharmacy and Pharmaceutical Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, GHANA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology, Faculty of Pharmacy and Pharmaceutical Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, GHANA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmaceutics, Faculty of Pharmacy and Pharmaceutical Sciences, Kwame Nkrumah University of Science and Technology, GHANA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Herbal Medicine, Faculty of Pharmacy and Pharmaceutical Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, GHANA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chinnapillai Arunachalam</style></author><author><style face="normal" font="default" size="100%">Balasundaram Maheshwari</style></author><author><style face="normal" font="default" size="100%">Govindarajan Nartunai</style></author><author><style face="normal" font="default" size="100%">Raju Ilavarasan</style></author><author><style face="normal" font="default" size="100%">Koppala Narayana Sunil Kumar</style></author><author><style face="normal" font="default" size="100%">Parameswaran Sathiyarajeswaran</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Pharmacognosy Approach to the Botanical Source of a Cinnamon Fruit Traded as Nāgakeśara and Sirunagappu in Raw Drug Markets</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">HPTLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Lauraceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Market substitute</style></keyword><keyword><style  face="normal" font="default" size="100%">Quality standards</style></keyword><keyword><style  face="normal" font="default" size="100%">Siddha</style></keyword><keyword><style  face="normal" font="default" size="100%">ulteration</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">81-87</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Background:&lt;/strong&gt; Adulteration and substitution of Nagakesara is a well-established fact in the medicinal plant literature though it is referred by the authors of important Ayurvedic texts to cure piles, dysentery, hiccup etc. The botanical identities of controversial sources of Nagakesara are flowers of Mesua ferrea L. and Ochrocarpus longifolius Benth. and Hook. f., &lt;em&gt;Calophyllum inophyllum&lt;/em&gt; L., Dillenia pentagyna Roxb. and perchance their allied species. Though immature fruits of some &lt;em&gt;Cinnamomum&lt;/em&gt; species are also reported to be sold as&lt;em&gt; Nagakesara/Sirunagappu&lt;/em&gt; in the crude drug markets there are no pharmacognostic studies available for the identification and analysis of this crude drug. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; In this study, marketed Nagakesara/ Sirunagappu samples were procured from Chennai raw drug market and analyzed as per the standard methodologies for pharmacognostic studies. &lt;strong&gt;Results:&lt;/strong&gt; Macro-microscopical characters and chemical identity of the samples of immature fruits were established to derive set of characters for the identification of this marketed material. The proposed results would help in identification of this crude drug while used as substitute drug for the official source. &lt;strong&gt;Conclusion:&lt;/strong&gt; The botanical Nagakesara or Sirunagappu is neither stamen nor flower, but it is fruit of &lt;em&gt;Cinnamomum&lt;/em&gt; species. As Western Ghats is habitat for several similar looking species of &lt;em&gt;Cinnamomum&lt;/em&gt;, there is necessity to study the pharmacognostical characters of all species of&lt;em&gt; Cinnamomum&lt;/em&gt; before concluding the botanical source of this ambiguous raw drug of Ayurveda and Siddha.&lt;/p&gt;

&lt;p&gt;&amp;nbsp;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">81</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Chinnapillai Arunachalam&lt;sup&gt;1&lt;/sup&gt;, Balasundaram Maheshwari&lt;sup&gt;1&lt;/sup&gt;, Govindarajan Nartunai&lt;sup&gt;1&lt;/sup&gt;, Raju Ilavarasan&lt;sup&gt;1&lt;/sup&gt;, Koppala Narayana Sunil Kumar&lt;sup&gt;1,2*&lt;/sup&gt;, Parameswaran Sathiyarajeswaran&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Captain Srinivasa Murthy Regional Ayurveda Drug Development Institute India, Chennai- 600106, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Siddha Central Research Institute, Arignar Anna Hospital Campus, Arumbakkam, Chennai- 600106, Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Meselhy KM</style></author><author><style face="normal" font="default" size="100%">Shams MM</style></author><author><style face="normal" font="default" size="100%">Sherif NH</style></author><author><style face="normal" font="default" size="100%">El-Sonbaty SM</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phenolic Profile and In Vivo Cytotoxic Activity of Rice Straw Extract</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cytotoxic</style></keyword><keyword><style  face="normal" font="default" size="100%">Histopathology</style></keyword><keyword><style  face="normal" font="default" size="100%">LC/MS/MS</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolics</style></keyword><keyword><style  face="normal" font="default" size="100%">Rice straw</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">849-857</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Previous work of our team exhibited that rice straw (RS) has antitumor activity &lt;em&gt;in vitro &lt;/em&gt;and inhibit proliferation of liver, lung, prostate, and breast cancer human cell lines. In this work, we extended our research to screen the antitumor activity of RS ethanol extract as a single treatment and in the presence of combined radiotherapy with a low dose of gamma radiation against murine Ehrlich solid carcinoma (EAC) model. &lt;strong&gt;Objective:&lt;/strong&gt; To evaluate the most common waste in Egypt RS to screen out its &lt;em&gt;in vivo&lt;/em&gt; cytotoxic activity and as combined therapy with radiotherapy.&lt;strong&gt; Method:&lt;/strong&gt; Tested sample RS was investigated for its content of phenolics by LC/MS/MS, in addition, ethanolic extracts of the tested sample were investigated as antitumor on female mice inoculated with EAC cells as a single treatment and in the presence of combined radiotherapy with a low dose of gamma radiation (LDR). &lt;strong&gt;Results:&lt;/strong&gt; LC/MS/MS revealed that rice straw was rich in phenolic acids (vanillic, p-coumaric, ferulic, and sinapic acid) along with catechin and flavonoids aglycones (quercetin, apigenin, and kaempferol). Rice straw and/or exposure to a low dose of γ-radiation caused a marked suppression of tumor growth and induced significant reduction in VEGF level &amp;amp; in IL-6 level with significant elevation in IL-10 serum level. Rice straw caused a significant down regulation in the gene transcription level of MCL1 and b-catenin, and a significant up-regulation of Caspase-3 and Bax gene expression. RS extract and LDR (EC + RS + R group) revealed that there was a mild form of necrosis with severe apoptosis in the tumor cells. &lt;strong&gt;Conclusion:&lt;/strong&gt; From the aforementioned results, it can be concluded that RS/LDR effectively and synergistically work towards inhibition of cancer cell proliferation. These findings were well supported with histopathological studies suggesting that RS/low dose gamma radiation can serve as a good therapeutic agent against cancer but still need further clinical studies.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">849</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Meselhy KM&lt;sup&gt;1,&lt;/sup&gt;*, Shams MM&lt;sup&gt;2&lt;/sup&gt;, Sherif NH&lt;sup&gt;3,4&lt;/sup&gt;, El-Sonbaty SM&lt;sup&gt;5&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, EGYPT.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medicinal Plants and Natural Products, National Organization for Drug Control &amp;amp; Research (NODCAR), Giza, EGYPT.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Drug Radiation Research Department, National Centre for Radiation Research and Technology (NCRRT), Atomic Energy Authority, Nasr City, EGYPT.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Pharmacognosy Department, Faculty of Pharmacy, Nahda University, Beni Suef, EGYPT.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Radiation Microbiology, The National Center for Radiation Research and Technology (NCRRT), Atomic Energy Authority, Nasr City, EGYPT.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dina Kanj</style></author><author><style face="normal" font="default" size="100%">Karim Raafat</style></author><author><style face="normal" font="default" size="100%">Abdalla El-Lakany</style></author><author><style face="normal" font="default" size="100%">Safaa Baydoun</style></author><author><style face="normal" font="default" size="100%">Maha Aboul-Ela</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Compounds Of Cichorium intybus by Exploring its Antioxidant and Antidiabetic Activities</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antidiabetic effects</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Cichorium Intybus</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Serum insulin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">248-257</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;!-- x-tinymce/html --&gt;&lt;strong&gt;Introduction&lt;/strong&gt;: The current study aims to evaluate the therapeutic effect of &lt;em&gt;Cichorium intybus&lt;/em&gt; n-hexane extract on &lt;em&gt;diabetes mellitus&lt;/em&gt; and its antioxidant effect &lt;em&gt;in vivo&lt;/em&gt; in alloxinated animals. Diabetic neuropathy improvement was also tested as well as insulin levels and histology of the pancreas were performed. &lt;strong&gt;Methods&lt;/strong&gt;: The chromatographic standardization of &lt;em&gt;C. intybus&lt;/em&gt; extract was performed using isocratic HPLC, which indicated the presence of numerous phyto-constituents. The hexane extract was studied for its effect on blood glucose levels and painful diabetic neuropathy (DN) in diabetic mice. Hyperalgesia and mechanical-allodynia were evaluated using thermal stimuli, pain response to radiant energy experiments and a mechanical sensitivity test respectively. Subsequently, after eight weeks of being alloxinated, BGL, body weight, antioxidant activity, insulin levels and glycated hemoglobin were recorded to evaluate antidiabetic potential and the DN. &lt;strong&gt;Results&lt;/strong&gt;: The administration of &lt;em&gt;Cichorium intybus&lt;/em&gt; extract (50, 75 and 100 mg/kg) and a combination of &lt;em&gt;Cichorium intybus&lt;/em&gt; extract and &lt;em&gt;Camellia sinensis&lt;/em&gt; (50 + 200 mg/kg, respectively) have revealed an acute hypoglycemic effect ranging from 14.15% and 42.4%. The sub-chronic anti-diabetic effect ranged from 23.41% and 44.8%. They diminished hyperalgesia and tangible allodynia significantly (p&amp;lt;0.05), (n=7 per group). The powerful neuroprotective properties might serve as potential lead-compounds for further analysis. &lt;strong&gt;Conclusion&lt;/strong&gt;: The histological study and the potent antioxidant effect showed that they could assist in the management of diabetes mellitus and DN by amelioration of insulin levels and regeneration of pancreatic beta cells.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">248</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;!-- x-tinymce/html --&gt;&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Dina Kanj&lt;sup&gt;1&lt;/sup&gt;, Karim Raafat&lt;sup&gt;1,&lt;/sup&gt;*, Abdalla El-Lakany&lt;sup&gt;1&lt;/sup&gt;, Safaa Baydoun&lt;sup&gt;2&lt;/sup&gt;, Maha Aboul-Ela&lt;sup&gt;1 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Sciences, Faculty of Pharmacy, Beirut Arab University, Beirut 115020, LEBANON.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Research Center for Environment and Development, Beirut Arab University, Taanayel, LEBANON.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Edwina O Uzunuigbe</style></author><author><style face="normal" font="default" size="100%">Foluso O Osunsanmi</style></author><author><style face="normal" font="default" size="100%">Priscilla Masamba</style></author><author><style face="normal" font="default" size="100%">Rebamang A Mosa</style></author><author><style face="normal" font="default" size="100%">Rebamang A Mosa</style></author><author><style face="normal" font="default" size="100%">Andrew R Opoku</style></author><author><style face="normal" font="default" size="100%">Abidemi P Kappo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Constituents and Antioxidant Activities of Crude Extracts from Acacia Senegal Leaf Extracts</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ABTS</style></keyword><keyword><style  face="normal" font="default" size="100%">Acacia Senegal</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidants</style></keyword><keyword><style  face="normal" font="default" size="100%">crude extract</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">Free Radicals</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1409-1414</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Acacia senegal&lt;/em&gt; (&lt;em&gt;Fabaceae&lt;/em&gt;) Wild is a leguminous tree with economic values, but its leaves are under-utilised. &lt;strong&gt;Objective:&lt;/strong&gt; To investigate the phytochemical constituents and antioxidant potential of crude extracts from &lt;em&gt;A. Senegal’s&lt;/em&gt; leaves. Methods: Methanol and acetone crude extracts of leaves of &lt;em&gt;A. senegal &lt;/em&gt;were prepared by maceration using organic solvents, methanol and acetone respectively. Qualitative and quantitative phytochemical analysis of the crude extracts were evaluated using Association of Agricultural and Chemist (AOAC) protocols. Antioxidant activities of the crude extracts were determined using 2, 2′-azino-bis-(3-ethylbenzothiazoline-6-sulphonic acid (ABTS) and 2, 2-diphenyl-1-picrylhydrazyl (DPPH) respectively. &lt;strong&gt;Results:&lt;/strong&gt; The crude extracts (acetone and methanol) showed vary quality of phytochemical constituent including flavonoid, alkaloids, carbohydrate, saponins, tannin, steroids, and terpenoids. Acetone crude possessed significant (&lt;em&gt;P&lt;/em&gt; &amp;lt; 0.05) higher total flavonoid and proanthocyanidin content in comparison with methanol extracts. Whereas, methanol crude extract possessed significant higher total phenol content compared with acetone crude extract. The crude extracts showed antioxidant activities as evidence in scavenging ABTS and DPPH radicals. However, acetone crude with lower IC&lt;sub&gt;50&lt;/sub&gt; of 0.09 mg/mL possessed significant higher ABTS scavenging ability compared to methanol (0.07 mg/mL) and ascorbic acid (0.07 mg/mL). &lt;strong&gt;Conclusion: &lt;/strong&gt;The crude extracts could serve as a promising natural antioxidant agent in management of oxidative stress diseases. For further studies, bioactive compounds need to be ascertained.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1409</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Edwina O Uzunuigbe&lt;sup&gt;1,2,&lt;/sup&gt;*, Foluso O Osunsanmi&lt;sup&gt;3&lt;/sup&gt;, Priscilla Masamba&lt;sup&gt;1&lt;/sup&gt;, Rebamang A Mosa&lt;sup&gt;4&lt;/sup&gt;, Andrew R Opoku&lt;sup&gt;1&lt;/sup&gt;, Abidemi P Kappo&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Biotechnology and Structural Biochemistry (BSB) Group, Department of Biochemistry and Microbiology, University of Zululand, KwaDlangezwa 3886, KwaZulu-Natal, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Rubber Research Institute of Nigeria (RRIN), Iyanomo, P.M.B 1049, Benin City, Edo State, NIGERIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Agriculture Science, University of Zululand, KwaDlangezwa 3886, KwaZulu-Natal, SOUTH AFRICA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biochemistry, University of Pretoria, Private Bag X 20, Hatfield 0028, SOUTH AFRICA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pushpender Bhardwaj</style></author><author><style face="normal" font="default" size="100%">Mohan Singh Thakur</style></author><author><style face="normal" font="default" size="100%">Sahil Kapoor</style></author><author><style face="normal" font="default" size="100%">Ashwani Kumar Bhardwaj</style></author><author><style face="normal" font="default" size="100%">Ajay Sharma</style></author><author><style face="normal" font="default" size="100%">Shweta Saxena</style></author><author><style face="normal" font="default" size="100%">Om Prakash Chaurasia</style></author><author><style face="normal" font="default" size="100%">Raj kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Screening and Antioxidant Activity Study of Methanol Extract of Stems and Roots of Codonopsis clematidea from Trans-himalayan Region</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Codonopsis clematidea</style></keyword><keyword><style  face="normal" font="default" size="100%">Fructose</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS</style></keyword><keyword><style  face="normal" font="default" size="100%">MER</style></keyword><keyword><style  face="normal" font="default" size="100%">MES</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">536-546</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Aim:&lt;/strong&gt; The present report aimed to study the therapeutic and phytochemical properties of stems and roots of trans-himalayan plant &lt;em&gt;Codonopsis clematidea.&lt;/em&gt; &lt;strong&gt;Material and Methods:&lt;/strong&gt; The crude samples of stems and roots were explored for their chlorophyll, carotenoid and carbohydrate content in order to understand the matrix of these two plant parts. The extraction of phytochemicals was carried out by three different methods&lt;em&gt; viz&lt;/em&gt;. sonication, maceration and soxhlet in methanol to identify the best extraction method. Further, analysis of Total Flavonoid Content (TFC) and Total Polyphenolic Content (TPC) were carried out using rutin trihydrate and gallic acid as a reference standard. Antioxidant capacity was estimated using three methods viz. 1,1-diphenyl-2-picrylhydrazyl (DPPH), 2,2’-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical scavenging assay and Ferric Reducing Antioxidant Power (FRAP) assay. In addition to this, GC-MS analysis was also performed for the identification of volatile constituents of Methanol Extract of Stems (MES) and Methanol Extract of Roots (MER). &lt;strong&gt;Results: &lt;/strong&gt;The MES and Dimethylsulfoxide Extract of Stems (DES) were found to have higher Chlorophyll a (Ch&lt;sub&gt;a&lt;/sub&gt;) content in comparison to Chlorophyll b (Ch&lt;sub&gt;b&lt;/sub&gt;) and Carotenoids (C&lt;sub&gt;ca&lt;/sub&gt;). Carbohydrate profile showed that stems and roots have the highest content of fructose in comparison to other sugar moieties. The soxhlet method showed the highest percentage extractive yield in the stems as well as roots. Results revealed that the MES showed higher antioxidant potential as compared to the MER. A correlation has also found to exist between the results of TPC, TFC and antioxidant assays, since TPC and TFC are key constituents responsible for the antioxidant potential. &lt;strong&gt;Conclusion: &lt;/strong&gt;These results have been found to suggest the richness of MES in natural phenols, flavonoids and antioxidants. Further, study should be conducted over identification and characterization of compounds present in the extract.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">536</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Pushpender Bhardwaj&lt;sup&gt;1&lt;/sup&gt;, Mohan Singh Thakur&lt;sup&gt;1&lt;/sup&gt;, Sahil Kapoor&lt;sup&gt;1&lt;/sup&gt;, Ashwani Kumar Bhardwaj&lt;sup&gt;1&lt;/sup&gt;, Ajay Sharma&lt;sup&gt;2&lt;/sup&gt;, Shweta Saxena&lt;sup&gt;1&lt;/sup&gt;, Om Prakash Chaurasia&lt;sup&gt;1&lt;/sup&gt;, Raj Kumar&lt;sup&gt;1,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Medicinal Plant, Defence Institute of High-Altitude Research c/o 56 APO, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemistry, Sant Longowal Institute of Engineering and Technology, Longowal, Sangrur, Punjab-148106, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Imad M Al-Ani</style></author><author><style face="normal" font="default" size="100%">Norsidah Ku-Zaifah</style></author><author><style face="normal" font="default" size="100%">Fakhria A. Al-Joufi</style></author><author><style face="normal" font="default" size="100%">Rafidah H.Mokhtar</style></author><author><style face="normal" font="default" size="100%">Norlelawati A. Talib</style></author><author><style face="normal" font="default" size="100%">Ghasak Ghazi Faisal</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Protective Role of Eurycoma longifolia Jack Root Extract Against High-Fat Diet Induced Testicular Damage in Sprague-Dawley Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Eurycoma Longifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">High-Fat-Diet</style></keyword><keyword><style  face="normal" font="default" size="100%">Seminiferous Tubules Tongkat Ali</style></keyword><keyword><style  face="normal" font="default" size="100%">Testis</style></keyword><keyword><style  face="normal" font="default" size="100%">Testosterone</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">808-811</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective: &lt;/strong&gt;The aims of this study were to investigate the adverse effects of the high-fat-diet (HFD) on the testosterone level and testicular structure of male rats as well as to examine whether &lt;em&gt;Eurycoma longifolia&lt;/em&gt; (EL) is able to ameliorate these effects. &lt;strong&gt;Methods:&lt;/strong&gt; Twenty-four male Sprague-Dawley (SD) rats were divided into four groups each containing 6 rats. Group ND was given only normal diet, group NDEL was given normal diet and EL extracts (15 mg/ kg) dissolved in distilled water, group HFD was given only high-fat-diet and group HFDEL was given high-fat-diet and EL extracts (15 mg/kg). EL was administered orally for 12 weeks. The animal’s testosterone level was measured at week 0, 6 and 12. The rats were sacrificed at the end of 12&lt;sup&gt;th &lt;/sup&gt;weeks and the testes samples were processed for histological examination&lt;strong&gt; Results: &lt;/strong&gt;The testosterone level was significantly increased (&lt;em&gt;p&lt;/em&gt; &amp;lt; 0.05) in the in the treated rats with EL (NDEL and HFDEL) compared with ND and HFD groups. Treatment with HFD revealed a marked degeneration of the seminiferous tubule epithelium and disruption of interstitial cells of the testis thereby interfering with spermatogenesis. Treatment of HFD rats with El reduced the adverse effects of HFD and improved the morphological structure of the seminiferous tubules. &lt;strong&gt;Conclusion: &lt;/strong&gt;These findings revealed that EL has ameliorative effects against the testicular damage caused by high-fat-diet.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">808</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Imad M Al-Ani&lt;sup&gt;1&lt;/sup&gt;, Norsidah Ku-Zaifah&lt;sup&gt;2&lt;/sup&gt;, Fakhria A. Al- Joufi&lt;sup&gt;3&lt;/sup&gt;, Rafidah H.Mokhtar&lt;sup&gt;4&lt;/sup&gt;, Norlelawati A. Talib&lt;sup&gt;5&lt;/sup&gt;, Ghasak Ghazi Faisal&lt;sup&gt;6,&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Dentistry, Al-Hikmah University College, Al-Yarmook, Baghdad, IRAQ.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Basic Medical Sciences, Kulliyyah of Medicine, International Islamic University, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;College of Pharmacy, Al Jouf University, Aljouf, Skaka KSA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Faculty of Medicine, Universiti Sains Islam Malaysia, Nilai, Negeri Sembilan, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Pathology and Laboratory Medicine, Kulliyyah of Medicine, International Islamic University, MALAYSIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Department of Fundamental Dental and Medical sciences, Kulliyyah of Dentistry, International Islamic University, MALAYSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chethankumara Ganadhal Puttaramaiah</style></author><author><style face="normal" font="default" size="100%">Krishna Venkatarangaiah</style></author><author><style face="normal" font="default" size="100%">Nagaraj Kakanahalli</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Screening In vitro Anticancer Activity of Alseodaphne semecarpifolia Nees Stem Bark Extracts against some Cancer Cell lines</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alseodaphne semecarpifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">Carcinoma</style></keyword><keyword><style  face="normal" font="default" size="100%">Cell lines</style></keyword><keyword><style  face="normal" font="default" size="100%">Cell viability</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Lymphoma</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">884-888</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Cancer is considered as the prime lethal disease that affects different organs of the body. Even with the rapid developments in the medical sciences, there are no proper medicines to cure specific kind of cancer without side effects. The inhibition of tumour cell growth without side effects either by the use herbal or synthetic drugs is considered as an important target in cancer therapy. In traditional medicinal system &lt;em&gt;A. semecarpifolia&lt;/em&gt; stem bark is the prime source of herbal drug to treat lymphatic and skin cancers. &lt;strong&gt;Objective:&lt;/strong&gt; The purpose of this study is to evaluate the anticancer potential of &lt;em&gt;A. semecarpifolia&lt;/em&gt; stem bark extracts against some cancer cell lines. &lt;strong&gt;Methods:&lt;/strong&gt; The&lt;em&gt; in vitro&lt;/em&gt; anticancer activity was evaluated against DLA, EAC, HeLa, HepG2 and L929 cell lines by trypan blue dye exclusion assay and SRB assay. &lt;strong&gt;Results:&lt;/strong&gt; The results of the anticancer activity revealed that, when compared to standard drug Cyclophosphamide, SBPEE and SBCE of A. semecarpifolia showed significant anticancer activity against DLA and EAC cell lines, without causing any toxicity to the normal mouse fibroblast cells L929. Whereas, none of the three extracts showed cytotoxicity against HeLa, HepG2 and L929 cell lines. &lt;strong&gt;Conclusion: &lt;/strong&gt;The present study suggested that, SBPEE and SBCE possesses significant cytotoxic activity against DLA and EAC cell lines, which confirms the traditional medicinal claim of &lt;em&gt;A. semecarpifolia&lt;/em&gt; as a potent anticancer plant against lymphatic and skin cancer.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">884</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Chethankumara Ganadhal Puttaramaiah&lt;sup&gt;1&lt;/sup&gt;, Krishna Venkatarangaiah&lt;sup&gt;2&lt;/sup&gt;, Nagaraj Kakanahalli&lt;sup&gt;3,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Research Scholar, Department of PG Studies and Research in Applied Zoology, Kuvempu University, Shivamogga, Karnataka, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Professor, Department of PG Studies and Research in Biotechnology, Kuvempu University, Shivamogga, Karnataka, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Professor, Department of PG Studies and Research in Applied Zoology, Kuvempu University, Shivamogga, Karnataka, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Muhammad Nursid</style></author><author><style face="normal" font="default" size="100%">Endar Marraskuranto</style></author><author><style face="normal" font="default" size="100%">Azizah Kuswardini</style></author><author><style face="normal" font="default" size="100%">Tjahyo Winanto</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Screening of Tyrosinase Inhibitor, Antioxidant and Cytotoxicity of Dried Sea Cucumber from Tomini Bay, Indonesia</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Screening</style></keyword><keyword><style  face="normal" font="default" size="100%">Sea cucumber</style></keyword><keyword><style  face="normal" font="default" size="100%">Tyrosinase inhibitor</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">555-558</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Indonesia, as a tropical country, is one of the important producers of sea cucumbers (beche-de-mer). Sea cucumber is a marine invertebrate that contains attractive bioactive secondary metabolites and these metabolites can be used for health as well as cosmetics. &lt;strong&gt;Objective:&lt;/strong&gt; The aim of the study was to determine the activity of tyrosinase inhibitors, antioxidants, and cytotoxicity of sea cucumber methanolic extract. &lt;strong&gt;Methods:&lt;/strong&gt; Dried sea cucumber samples were taken from Boalemo waters, Tomini Bay, Indonesia. Tyrosinase inhibitor assay was carried out spectrophotometrically using tyrosinase enzymes and L-DOPA as a substrate and antioxidant tests were carried out by DPPH method. Cytotoxicity test against human breast cancer cell line (T47D) was conducted using the MTT assay. &lt;strong&gt;Results:&lt;/strong&gt; The study showed that &lt;em&gt;Bohadschia vitiensis&lt;/em&gt; had the best tyrosinase inhibitor activity with IC&lt;sub&gt;50&lt;/sub&gt; value of 0.28 mg/ml. The DPPH free radical scavenging testing showed that all sea cucumbers had weak antioxidant activity. On the other hand, cytotoxicity assay revealed that several sea cucumbers had good cytotoxicity against T47D cells, where &lt;em&gt;Holothuria atra&lt;/em&gt; and &lt;em&gt;Bohadschia marmorata &lt;/em&gt;showed strong cytotoxicities with IC&lt;sub&gt;50&lt;/sub&gt; values of 23.0 and 28.1 ug/mL, respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; Based on the study, it can be concluded that the dried sea cucumber from the Tomini bay region, Indonesia, has the potential to be developed as a source of tyrosinase inhibitors and cytotoxic agents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">555</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Muhammad Nursid&lt;sup&gt;1,*&lt;/sup&gt;, Endar Marraskuranto&lt;sup&gt;1&lt;/sup&gt;, Azizah Kuswardini&lt;sup&gt;2&lt;/sup&gt;, Tjahyo Winanto&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Research Center for Marine and Fisheries Product Processing and Biotechnology, Ministry of Marine and Fisheries Affairs, REPUBLIC OF INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Marine and Fisheries Science, University of Jenderal Soedirman, Purwokerto, INDONESIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shikha Rangra Chandel</style></author><author><style face="normal" font="default" size="100%">Vikas Kumar</style></author><author><style face="normal" font="default" size="100%">Shikha Guleria</style></author><author><style face="normal" font="default" size="100%">Nitin Sharma</style></author><author><style face="normal" font="default" size="100%">Anuradha Sourirajan</style></author><author><style face="normal" font="default" size="100%">Prem Kumar Khosla</style></author><author><style face="normal" font="default" size="100%">David J. Baumler</style></author><author><style face="normal" font="default" size="100%">Kamal Dev</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sequential Fractionation by Organic Solvents Enhances the Antioxidant and Antibacterial Activity of Ethanolic Extracts of Fruits and Leaves of Terminalia bellerica from North Western Himalayas, India</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimicrobial</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethanolic extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Fruits</style></keyword><keyword><style  face="normal" font="default" size="100%">Leaves</style></keyword><keyword><style  face="normal" font="default" size="100%">Terminalia bellerica</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">94-101</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Terminalia bellerica&lt;/em&gt; belonging to family combretaceae is one of the major components of “Triphala”, an Ayurvedic formulation. &lt;strong&gt;Objective:&lt;/strong&gt; To evaluate antioxidant potential in the ethanolic extract and its active fraction (chloroform, ethyl acetate, n- butanol and aqueous fraction) from fruits and leaves of&lt;em&gt; Terminalia bellerica&lt;/em&gt;. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Folin-Ciocalteau method and aluminium chloride method was used to quantify total phenolic and flavonoid content respectively in ethanolic extract and their fractions from fruits and leaves of &lt;em&gt;T. bellerica&lt;/em&gt;. The antioxidant activity was evaluated using total antioxidant activity, DPPH, FRAP and total antioxidant activity methods. &lt;strong&gt;Results:&lt;/strong&gt; Total phenolics (254.72±3.03 mg/g GAE and 227.52±1.38 mg/g GAE) and flavonoids (64.77±1.24 mg/gm RE and 75.57±1.38 mg/gm RE) content was higher in ethyl acetate fraction of both fruits and leaves sample of &lt;em&gt;T. bellerica&lt;/em&gt;, respectively. The order of free radical scavenging activities was ethyl acetate fraction &amp;gt; crude ethanolic extract &amp;gt; n-butanol fraction &amp;gt; chloroform fraction &amp;gt; aqueous fraction. Similarly, ethyl acetate fraction of both fruits and leaves exhibited more antimicrobial activity as compared to that of ethanolic extract as revealed from agar well diffusion method with diameter of zone of inhibi¬tion of 14.0±1.41 mm, 21.0±1.41 mm, 14.0±1.41 mm, 14.5±0.71 mm in fruits and 18.0±1.41 mm, 22.5±2.12 mm, 15.5±2.12 mm, 14.5±3.53 mm in leaves against &lt;em&gt;B. subtilis&lt;/em&gt;,&lt;em&gt; S. aureus,&lt;/em&gt; &lt;em&gt;E. coli&lt;/em&gt;, &lt;em&gt;K. pneumoniae&lt;/em&gt;, respectively. MIC values for fruits were 3.125 mg/ml, 0.375 mg/ml, 3.125 mg/ml, 3.125 mg/ml and for leaves were 1.5625 mg/ml, 0.19 mg/ml, 0.78 mg/ ml, 0.78 mg/ml against &lt;em&gt;B. subtilis,&lt;/em&gt; &lt;em&gt;S. aureus,&lt;/em&gt; &lt;em&gt;E. coli, K. pneumoniae&lt;/em&gt;, respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; The present study provides the evidence for comparative antioxidant and antibacterial potential of ethanolic extracts of fruits and leaves of &lt;em&gt;T. bellerica&lt;/em&gt;. . Moreover, leaves can be promoted to be used for therapeutics and natural antioxidants.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">94</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Shikha Rangra Chandel&lt;sup&gt;1&lt;/sup&gt;, Vikas Kumar&lt;sup&gt;1&lt;/sup&gt;, Shikha Guleria&lt;sup&gt;1&lt;/sup&gt;, Nitin Sharma&lt;sup&gt;2&lt;/sup&gt;&lt;sub&gt;,&amp;nbsp;&lt;/sub&gt;Anuradha Sourirajan&lt;sup&gt;1&lt;/sup&gt;, Prem Kumar Khosla&lt;sup&gt;1&lt;/sup&gt;, David J. Baumler&lt;sup&gt;3,4,5&lt;/sup&gt;, Kamal Dev&lt;sup&gt;1,3* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Applied Sciences and Biotechnology, Shoolini University, Post Box No. 9, Head Post Office, Solan, Himachal Pradesh, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biotechnology, Chandigarh Group of Colleges, Landran, Mohali, Punjab, INDIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Food Science and Nutrition, University of Minnesota-Twin Cities, St. Paul, MN, USA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Microbial and Plant Genome Institute, University of Minnesota-Twin Cities, St. Paul, MN, USA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Biotechnology Institute, University of Minnesota-Twin Cities, St. Paul, MN, USA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Marian Nabil</style></author><author><style face="normal" font="default" size="100%">Neveen S Ghaly</style></author><author><style face="normal" font="default" size="100%">Iman AA Kassem</style></author><author><style face="normal" font="default" size="100%">Mary H Grace</style></author><author><style face="normal" font="default" size="100%">Farouk R Melek</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Two Triterpenoid Saponins with alpha-glucosidase Inhibitory Activity from Harpullia pendula Seed Extract</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Harpullia pendula</style></keyword><keyword><style  face="normal" font="default" size="100%">Sapindaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Triterpenoid saponins</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1386-1390</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Harpullia pendula &lt;/em&gt;Planch (family Sapindaceae) is a small to medium rainforest tree native to Australia. &lt;strong&gt;Objective: &lt;/strong&gt;This study aims to isolate triterpenoid saponins from &lt;em&gt;H. pendula &lt;/em&gt;and test them as α-glucosidase inhibitors. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;The saponin compounds were obtained using variable chromatographic techniques and characterized by spectral analysis. &lt;strong&gt;Results:&lt;/strong&gt; Two new triterpenoid saponins were obtained as an inseparable mixture from &lt;em&gt;H. pendula&lt;/em&gt; methanolic seed extract. Their structures were determined as 3-O-β-D-glucopyranosyl-(1→2)-[α-L-arabinofuranosyl-(1→3)]-βD-glucuronopyranosyl22-OangeloylA1- barrigenol and 3-O-β-D-galactopyranosyl-(1→2)-[α-L-arabinofuranosyl-(1→3)]-β-Dglucuronopyranosyl 22-O-(2-methylbutyroyl)-A1 barrigenol, respectively. The triterpene part 22-O-(2-methyl butyroyl) A1-barrigenol has never been characterized before. The α- glucosidase inhibitory activity of the two saponin mixture was evaluated &lt;em&gt;invitro&lt;/em&gt; and proved to exhibit strong activity with IC&lt;sub&gt;50&lt;/sub&gt; value equals to 13.3 ± 5.0 ppm and IC&lt;sub&gt;90 &lt;/sub&gt;value equals to 21.5 ± 8.0 ppm. &lt;strong&gt;Conclusion: &lt;/strong&gt;Two new saponins were characterized from their mixture and found to exhibit α-glucosidase inhibitory activity.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1386</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Marian Nabil, Neveen S. Ghaly, Iman A.A. Kassem, Mary H. Grace and Farouk R. Melek* &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;Chemistry of Natural Compounds Department, National Research Centre, Dokki,12622, Giza, EGYPT.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hadi Kuncoro</style></author><author><style face="normal" font="default" size="100%">Aty Widyawaruyanti</style></author><author><style face="normal" font="default" size="100%">Taslim Ersam</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Alpha-Mangostin Effect on Inhibition Development Stadium and Globin Accumulation Against Plasmodium falciparum</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Development stage inhibition</style></keyword><keyword><style  face="normal" font="default" size="100%">Garcinia tetrandra</style></keyword><keyword><style  face="normal" font="default" size="100%">Plasmodium falciparum</style></keyword><keyword><style  face="normal" font="default" size="100%">SDS-PAGE</style></keyword><keyword><style  face="normal" font="default" size="100%">α-mangostin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/670</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">783-788</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&amp;alpha;--Mangostin is a widely reported group of Xanthone compounds from the Clusiaceae family of 40 genera and over 1000 species spread across the tropics and subtropics area. The Objective for determine effect of &amp;alpha;-mangostin from &lt;em&gt;Garcinia tetrandra&lt;/em&gt; Pierre stem bark against development stadium inhibition and globin accumulation of &lt;em&gt;Plasmodium falciparum&lt;/em&gt;. Inhibition stadium development assay used based on the Rosenthal method. &lt;em&gt;Plasmodium falciparum&lt;/em&gt; parasitic globin accumulation assay. Globin accumulation assay used the highest concentration of in vitro antimalarial test using SDS-PAGE with positive control E-64 and &amp;alpha;-mangostin were incubated together with the malaria parasite during 24 h. Result of Inhibition stadium development of Plasmodium falciparum against &amp;alpha;-mangostin show inhibition from development stadium of the malaria parasite &lt;em&gt;Plasmodium falciparum&lt;/em&gt;, Electrophoresis show globin accumulation from electrophoresis followed by staining using &lt;em&gt;Coomassie brilliant blue&lt;/em&gt;. &amp;alpha;-mangostin showed inhibition the growth of malaria parasite &lt;em&gt;Plasmodium falciparum&lt;/em&gt; with dose 10 &amp;mu;g/ml is expected to occur a large accumulation of globin, which can be viewed both morphologically and by the method of SDS-PAGE.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">783</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Hadi Kuncoro&lt;sup&gt;1&lt;/sup&gt;*, Aty Widyawaruyanti&lt;sup&gt;2&lt;/sup&gt;, Taslim Ersam&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Laboratorium Penelitian dan Pengembangan Kefarmasian FARMAKA TROPIS, Fakultas Farmasi, Mulawarman University, Samarinda 75119, East Kalimantan, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacognosy and Phytochemistry, Faculty of Pharmacy, Airlangga University, Surabaya, 60286, Indonesia, Center for Natural Product Medicine Research and Development, Institute of Tropical Disease, Airlangga University, Surabaya 60115, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Institut Teknologi Sepuluh November, Kampus ITS-Sukolilo, Surabaya 60111, INDONESIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amira Kamalrudin</style></author><author><style face="normal" font="default" size="100%">Malina Jasamai</style></author><author><style face="normal" font="default" size="100%">Mahanem Mat Noor</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ameliorative Effect of Moringa oleifera Fruit Extract on Reproductive Parameters in Diabetic-induced Male Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Diabetes mellitus</style></keyword><keyword><style  face="normal" font="default" size="100%">Fasting blood glucose level</style></keyword><keyword><style  face="normal" font="default" size="100%">Male reproductive</style></keyword><keyword><style  face="normal" font="default" size="100%">Moringa oleifera fruit</style></keyword><keyword><style  face="normal" font="default" size="100%">Sperm quality</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">s54-s58</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Diabetes mellitus negatively impact the male reproductive parameters. The ability of &lt;em&gt;Moringa oleifera&lt;/em&gt; fruit to improve the reproductive parameters in diabetic-induced male has yet to be documented. Aim: To investigate the anti-hyperglycaemic potential of &lt;em&gt;M. oleifera&lt;/em&gt; fruit aqueous extract and its effect on reproductive parameters in diabetic-induced male rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; A total of 20 male Sprague Dawley rats were divided into four groups; normal control (without diabetic induction), negative control (diabetes without treatment), positive control (diabetes with metformin) and treatment group (diabetes with 500 mg/kg &lt;em&gt;M. oleifera&lt;/em&gt; fruit aqueous extract). Treatments were given&lt;em&gt; via&lt;/em&gt; oral gavage for 21 consecutive days. Analysis of fasting blood glucose level, sperm quality, testicular histology and relative testis weight were performed. &lt;strong&gt;Results:&lt;/strong&gt; The administration of &lt;em&gt;M. oleifera&lt;/em&gt; fruit aqueous extract exhibited a significant reduction in fasting blood glucose level and a pronounced increase in sperm quality (sperm count, motility, viability and morphology) compared with the negative control group. &lt;em&gt;M. oleifera&lt;/em&gt; fruit extract restored the histology of the testes as they were seen to be packed with sperms and showed an organised spermatogenesis. The relative testis weight showed no significant difference between all groups. &lt;strong&gt;Conclusion:&lt;/strong&gt; The results obtained suggested that &lt;em&gt;M. oleifera&lt;/em&gt; fruit aqueous extract possessed an antihyperglycaemic property and improved the reproductive parameters in diabetic-induced rats&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s54</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Amira&lt;/strong&gt;&lt;strong&gt; Kamalrudin&lt;sup&gt;1&lt;/sup&gt;, Malina Jasamai&lt;sup&gt;2&lt;/sup&gt;, Mahanem Mat Noor&lt;sup&gt;1* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;School of Biosciences and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor, MALAYSIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt; 2&lt;/sup&gt;Drug and Herbal Research Centre, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, 50300, Kuala Lumpur, MALAYSIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nandan Padmanabha</style></author><author><style face="normal" font="default" size="100%">Nirupama Muralimunglimane</style></author><author><style face="normal" font="default" size="100%">Nayanatara Arun Kumar</style></author><author><style face="normal" font="default" size="100%">Bhagyalakshmi Kodavanji</style></author><author><style face="normal" font="default" size="100%">Jyoti Ramnath Kini</style></author><author><style face="normal" font="default" size="100%">Roopesh Poojary</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ameliorative Role of Vitamin D on Prenatal and Postnatal Exposure of Monosodium Glutamate Induced Steatohepatitis in Rat Pups</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Gestation</style></keyword><keyword><style  face="normal" font="default" size="100%">Glutamate</style></keyword><keyword><style  face="normal" font="default" size="100%">MSG</style></keyword><keyword><style  face="normal" font="default" size="100%">Steatohepatisis</style></keyword><keyword><style  face="normal" font="default" size="100%">Vitamin D</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/493</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">371-375</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Monosodium glutamate (MSG) is a widely used flavor enhancer has been linked to obesity and metabolic syndrome, including progressive liver disease. Nonalcoholic Fatty Liver Disease (NAFLD) is the most common hepatic disorder with an etiology related to changes in diet and lifestyle. Prenatal and postnatal exposure to MSG been shown to affect developing tissues in growing animals. Increased Risk of Non-alcoholic Steatohepatitis has been associated with Vitamin D deficiency. The present study was aimed to investigate the ameliorative effect of vitamin D on MSG induced animal models of steatohepatitis in neonatal rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Eighteen nulliparous female wistar rats were randomly divided into three groups (n=6/group). Group-I received a daily oral dose of 5g/kg body weight of MSG. Group-II received the same dose of MSG along with calcitriol (0.2&amp;mu;g/kg BW). Group-III was treated with saline served as the control. The rats could mate, and treatment was given for the entire period of gestation and thirty days thereafter, during lactation. The histological changes in the liver was observed. &lt;strong&gt;Results:&lt;/strong&gt; Pan-lobular microvesicular steatosis, lobular inflammation and ballooning of hepatocytes was observed in the MSG-treated group. These histotoxic changes were ameliorated in the vitamin D treated group. &lt;strong&gt;Conclusion:&lt;/strong&gt; Vitamin D might be beneficial in the protection of the pre-and postnatal exposed MSG induced steatohepatitis. Further, induction of steatohepatitis in a shorter period could also make it an ideal study model of non-alcoholic steatohepatitis.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">371</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Nandan Padmanabha&lt;sup&gt;1&lt;/sup&gt;, Nirupama Muralimunglimane&lt;sup&gt;2&lt;/sup&gt;, Nayanatara Arun Kumar&lt;sup&gt;3&lt;/sup&gt;*, Bhagyalakshmi Kodavanji&lt;sup&gt;3&lt;/sup&gt;, Jyoti Ramnath Kini&lt;sup&gt;2&lt;/sup&gt;, Roopesh Poojary&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Medical Student, Final MBBS-1, Kasturba Medical College Mangalore, Manipal Academy of Higher Education (MAHE), Karnataka, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pathology, Kasturba Medical College, Manipal Academy of Higher Education (MAHE), Mangalore, Karnataka, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Physiology, Kasturba Medical College, Manipal Academy of Higher Education (MAHE), Mangalore, Karnataka, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Senior Research Fellow, Department of Physiology. Kasturba Medical College, Mangalore, Manipal Academy of Higher Education (MAHE), Karnataka, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Krishnaprasad Ganapati Koorse</style></author><author><style face="normal" font="default" size="100%">Sujith Samraj</style></author><author><style face="normal" font="default" size="100%">Preethy John</style></author><author><style face="normal" font="default" size="100%">Priya Manakkulaparambil Narayanan</style></author><author><style face="normal" font="default" size="100%">Devi SS</style></author><author><style face="normal" font="default" size="100%">Usha PTA</style></author><author><style face="normal" font="default" size="100%">Surya Sunilkumar</style></author><author><style face="normal" font="default" size="100%">Gleeja VL</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anthelmintic Activity of Fruit Extract and Fractions of Piper longum L. In vitro</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adulticidal</style></keyword><keyword><style  face="normal" font="default" size="100%">GCMS</style></keyword><keyword><style  face="normal" font="default" size="100%">IC50</style></keyword><keyword><style  face="normal" font="default" size="100%">Larvicidal</style></keyword><keyword><style  face="normal" font="default" size="100%">Ovicidal</style></keyword><keyword><style  face="normal" font="default" size="100%">Piper longum.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/487</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">333-340</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;The present study was aimed to assess the &lt;em&gt;in vitro&lt;/em&gt; ovicidal, larvicidal and adulticidal activity of methanolic extract and its fractions from fruits of &lt;em&gt;Piper longum&lt;/em&gt; against strongyle ova, larvae and adult amphistomes respectively. The fruits of &lt;em&gt;P. longum&lt;/em&gt; was identified and the accession number 006 was obtained. The phytochemical analysis revealed the presence of tannins, flavonoids, glycosides, phenolics, diterpenes and triterpenes in extract and fractions of &lt;em&gt;P. longum&lt;/em&gt;. The extract and fractions were diluted serially in 6.25 per cent tween 80 to obtain concentrations of 500, 250, 125, 62.5, 31.25, 15.63, 7.81, 3.91 and 1.95 mg/mL. Ivermectin and thiabendazole at 10 &amp;mu;g/mL acted as positive controls and 6.25 per cent tween 80 as negative control. The methanolic extract was highly active against ova with IC&lt;sub&gt;50&lt;/sub&gt; of 0.026 mg/mL. The n-hexane fraction was potent in inducing larval mortality with IC&lt;sub&gt;50&lt;/sub&gt; of 1.383 mg/mL while chloroform fraction inhibited larval migration with IC&lt;sub&gt;50&lt;/sub&gt; of 1.796 mg/mL. Amphistomes were highly sensitive for methanolic extract of &lt;em&gt;P. longum&lt;/em&gt; which possessed IC&lt;sub&gt;50&lt;/sub&gt; of 5.493 mg/mL Based on IC&lt;sub&gt;50&lt;/sub&gt; values, the methanolic extract was found to be most potent while chloroform fraction was effective against ova, larvae and also adults. GCMS analysis of potent methanolic extract revealed the presence of piperidinone, hydrocinnamic acid, ethylhexahydro azepine, methyleugenol, hexadecanoic acid and caryophyllene oxide which may have contributed for the anthelmintic activity. The acute oral toxicity study revealed mild vascular changes in liver. From the present study, it can be concluded that chloroform fraction of &lt;em&gt;P. longum&lt;/em&gt; possessed maximum broad spectrum anthelmintic activity comparable to controls.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">333</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Krishnaprasad Ganapati Koorse&lt;sup&gt;1&lt;/sup&gt;*, Sujith Samraj&lt;sup&gt;1&lt;/sup&gt;, Preethy John&lt;sup&gt;1&lt;/sup&gt;, Priya Manakkulaparambil Narayanan&lt;sup&gt;2&lt;/sup&gt;, Devi SS&lt;sup&gt;3&lt;/sup&gt;, Usha PTA&lt;sup&gt;1&lt;/sup&gt;, Surya Sunilkumar&lt;sup&gt;1&lt;/sup&gt;, Gleeja VL&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Veterinary Pharmacology and Toxicology, College of Veterinary and Animal Sciences, Mannuthy, Thrissur, Kerala, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Veterinary Parasitology, College of Veterinary and Animal Sciences, Mannuthy, Thrissur, Kerala, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;3Department of Veterinary Pathology, College of Veterinary and Animal Sciences, Mannuthy, Thrissur, Kerala, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Statistics, College of Veterinary and Animal Sciences, Mannuthy, Thrissur, Kerala, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gaurav Sharma</style></author><author><style face="normal" font="default" size="100%">Sunil Kumar</style></author><author><style face="normal" font="default" size="100%">Megha Sharma</style></author><author><style face="normal" font="default" size="100%">Navneet Upadhyay</style></author><author><style face="normal" font="default" size="100%">Sunil Kumar</style></author><author><style face="normal" font="default" size="100%">Zabeer Ahmed</style></author><author><style face="normal" font="default" size="100%">Neeraj Mahindroo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anti-Diabetic, Anti-Oxidant and Anti-Adipogenic Potential of Quercetin Rich Ethyl Acetate Fraction of Prunus persica</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-adipogenic</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-diabetic</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-oxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Prunus persica</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercetin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/509</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">463-469</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Diabetes mellitus is enfeebling threatening diseases with continuously increasing rates of incidence and mortality and it may rise tremendously by 2025. &lt;strong&gt;Objective:&lt;/strong&gt; Quercetin rich ethyl acetate fraction (PP-EtOA) of leaves of &lt;em&gt;Prunus persica&lt;/em&gt; was evaluated for antidiabetic, anti-oxidant and anti-adipogenic activities. Material and Methods: Streptozotocin (STZ)-induced diabetic rat model, oral glucose tolerance test (OGTT) and normalglycemic rat models were investigated at the doseof 100 and 200 mg/kg,&lt;em&gt;p.o&lt;/em&gt;. of PP-EtOA. &lt;strong&gt;Results:&lt;/strong&gt; At 200 mg/kg, significant anti-hyperglycaemic activity(&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05) was observed in all the rat models. In STZ induced diabetic rat model, improvement in body weight and lipid profile was also observed.DPPH (2,2&amp;rsquo;-diphenyl-1-picrylhydrazyl) free radical scavenging method showed dose dependent scavenging. Preadipocyte differentiation assay (3T3-L1) showed significant inhibition of differentiation. HPLC fingerprinting analysis of fraction was also performed. &lt;strong&gt;Conclusion:&lt;/strong&gt; PP-EtOA possesses potent free radical scavenging property. Its antihyperglycemic and antiadipogenic activities may be due to quercetin (flavonoid) and may prove to be effective in the treatment of diabetes mellitus and diabetes driven dyslipidemic conditions.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">463</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Gaurav Sharma&lt;sup&gt;1*&lt;/sup&gt;, Sunil Kumar&lt;sup&gt;1&lt;/sup&gt;, Megha Sharma&lt;sup&gt;1&lt;/sup&gt;,&amp;nbsp;Navneet Upadhyay&lt;sup&gt;1&lt;/sup&gt;, Sunil Kumar&lt;sup&gt;2&lt;/sup&gt;, Zabeer Ahmed&lt;sup&gt;3&lt;/sup&gt;, Neeraj Mahindroo&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;School of Pharmaceutical Sciences, Shoolini University, Solan, Himachal Pradesh, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medical Parasitology, Post Graduate Institute of Medical Education and Research, Chandigarh, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Division of Pharmacology, Indian Institute of Integrative Medicine (CSIR), Jammu, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Greeshma Geetha Mohandas</style></author><author><style face="normal" font="default" size="100%">Murugan Kumaraswamy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antioxidant Activities of Terpenoids from Thuidium tamariscellum (C. Muell.) Bosch. and Sande-Lac. a Moss</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Moss</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenols</style></keyword><keyword><style  face="normal" font="default" size="100%">Terpenoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Thuidium tamariscellum</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/644</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">645-649</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Thuidium tamariscellum&lt;/em&gt; is a small creeping epiphytic moss growing on trunks and branches of trees as well as on moist shady rocky surface at high altitudes areas.&lt;strong&gt; Methods:&lt;/strong&gt; The present study was undertaken to analyze the phytochemicals in the species and its antioxidant potentialities interms of DPPH, ABTS, H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;, FRAP and metal chelating ability. &lt;strong&gt;Results:&lt;/strong&gt; Total terpenoids level was remarkable. Interestingly, a concentration dependent free radical scavenging potential was noticed and was comparable with the synthetic antioxidant ascorbate. Further, the FTIR analysis of petroleum ether, chloroform, ethyl acetate, and methanol extract confirmed the presence of alcohols/phenols, primary, secondary amines, amides, alkanes, aldehydes, saturated aliphatic alkenes aromatics and aromatic amines, nitro compounds, carboxylic acids, esters, ethers, aliphatic amines, alkyl halides and carbonyls in the moss indicating the presence of medicinally important compounds like flavonoids, terpenoids and alkaloids in the various solvent extracts of the moss. &lt;strong&gt;Conclusion:&lt;/strong&gt; The overall result of the present study showed that the moss is rich in important pharmaceutical compounds and was reflected as its antioxidant potential. Further studies are warranted to isolate, identify and purify the lead terpenoid present in the moss.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">645</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Greeshma Geetha Mohandas&lt;sup&gt;1&lt;/sup&gt;, Murugan Kumaraswamy&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;2&lt;/strong&gt; &lt;/sup&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Botany, University College&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Botany and Biotechnology, Govt. Arts College, Thiruvananthapuram, Kerala, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rekha Durgadas Kini</style></author><author><style face="normal" font="default" size="100%">Nayanatara Arun Kumar</style></author><author><style face="normal" font="default" size="100%">Anupama Noojibail</style></author><author><style face="normal" font="default" size="100%">Bhagyalakhshmi K</style></author><author><style face="normal" font="default" size="100%">Sneha Shetty Bhoja</style></author><author><style face="normal" font="default" size="100%">Pratik Kumar Chatterjee</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antioxidant Role of Beta Carotene: Protection against Cadmium Induced Testicular Toxicity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Lipid peroxidation</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidative stress</style></keyword><keyword><style  face="normal" font="default" size="100%">Superoxide demutase</style></keyword><keyword><style  face="normal" font="default" size="100%">Testis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">s66-s70</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Cadmium (Cd) is an industrial pollutant that affects the male reproductive system. The purpose of present study was to investigate the protective role of Beta carotene on cadmium induced testicular damage. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The present study was conducted following approval from Institutional Bioethical Committee and strict internationally accepted guidelines, for the usage of animals in experimental study were. Rats were divided into four groups with 8 rats in each.The Gr. I rats were administered with the single dose of normal saline intraperitoneally. Group II received Beta carotene (10 mg/kg bw) orally for 30 days. Group III received a single dose of 1 mg/kg bw cadmium chloride and Group IV received Beta carotene for 30 days prior to cadmium administration. After the desired protocol, rats were sacrificed and both the testes were removed for biochemical and histopathological evaluation. One testis was fixed in Bouvins fluid and processed or histopathological studies. The levels of lipid peroxides (LPO) and glutathione (GSH) and superoxide dismutase (SOD) were detected in the tissue homogenates of other testis. &lt;strong&gt;Results:&lt;/strong&gt; In the present study, the level of lipid peroxidation (LPO) was significantly high and GSH and SOD (&lt;em&gt;P&lt;/em&gt;&amp;lt;0.001) were low in cadmium treated rats compared to normal control. Pre-treatment with beta carotene showed a protective effect by decreasing LPO and increasing GS Hand SOD level (&lt;em&gt;P&lt;/em&gt;&amp;lt;0.001). The morphological changes like atrophy of tubules, edema and decreased spermatogenesis in the testis of rats exposed to cadmium chloride. But, antioxidant showed the normal architecture of the testis. &lt;strong&gt;Conclusion:&lt;/strong&gt; Results of the present study showed the antioxidative role of beta carotene in protecting the testis from cadmium induced toxicity.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s66</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Rekha Durgadas Kini&lt;sup&gt;*&lt;/sup&gt;, Nayanatara Arun Kumar, Anupama Noojibail, Bhagyalakhshmi K, Sneha Shetty Bhoja, Pratik Kumar Chatterjee &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Physiology, Kasturba Medical College, Manipal Academy of Higher Education (MAHE), Mangalore, INDIA&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hayat Mohammad Mukhtar</style></author><author><style face="normal" font="default" size="100%">Amandeep Singh</style></author><author><style face="normal" font="default" size="100%">Hardeep Kaur</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bioassay Guided Fractionation and in vitro Anti-plasmodial Activity of Ficus deltoidea and Ficus benjamina</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antiplasmodial</style></keyword><keyword><style  face="normal" font="default" size="100%">Bioassay guided fractionation</style></keyword><keyword><style  face="normal" font="default" size="100%">Ficus deltoidea Ficus benjamina</style></keyword><keyword><style  face="normal" font="default" size="100%">Malaria</style></keyword><keyword><style  face="normal" font="default" size="100%">Schizont maturation inhibition assay</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/471</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">235-240</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Malaria is infectious vector born disease affecting 212 million people belonging to 97 countries globally in the year 2016. Although this number has reduced progressively from last one decade but recent failure of currently available antimalarial drug therapy has accentuated the urgent need to explore different novel approaches in &lt;em&gt;Anti-plasmodial&lt;/em&gt; drug discovery. Objective: The aim of the present study was to evaluate the &lt;em&gt;Anti-plasmodial&lt;/em&gt; activity of traditional medicinal plants &lt;em&gt;Ficus deltoidea and Ficus benjamina&lt;/em&gt;. Materials and Methods: Crude petroleum ether and hydro alcoholic extract of both the plant species were evaluated for &lt;em&gt;Anti-plasmodial&lt;/em&gt; activity by schizont maturation inhibition assay using 3D7 &lt;em&gt;plasmodium&lt;/em&gt; strains. Results: It was observed that petroleum ether extract of &lt;em&gt;F. benjamina &lt;/em&gt;leaves showed most promising inhibitory effect on the growth of schizonts with IC&lt;sub&gt;50&lt;/sub&gt; 14.5 &amp;mu;g/ml. Bio-assay guided fractionation of petroleum ether extract of &lt;em&gt;F. benjamina&lt;/em&gt; led to the hexane and chloroform fraction with high &lt;em&gt;Anti-plasmodial&lt;/em&gt; activity (IC&lt;sub&gt;50&lt;/sub&gt; 4.0 &amp;mu;g/ml and IC&lt;sub&gt;50&lt;/sub&gt; 7.8 &amp;mu;g/ml respectively). Further, phytochemical investigation of &lt;em&gt;F. benjamina&lt;/em&gt; indicated the presence of various valuable phytochemicals belonging to class of steroids, terpenoids and phytosterols. Conclusion: This study has revealed the &lt;em&gt;Anti-plasmodial&lt;/em&gt; activity of F. deltoidea and &lt;em&gt;F. benjamina&lt;/em&gt; for the first time. Significant &lt;em&gt;Anti-plasmodial&lt;/em&gt; activity and preliminary phytochemical studies of &lt;em&gt;F. benjamina&lt;/em&gt; indicates its rich chemical diversity which make this plant a good candidate for isolating new molecule that could serve as new lead in &lt;em&gt;Anti-plasmodial&lt;/em&gt; drug discovery.&amp;nbsp;&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">235</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Hayat Mohammad Mukhtar&lt;sup&gt;1&lt;/sup&gt;, Amandeep Singh&lt;sup&gt;2&lt;/sup&gt;*, Hardeep Kaur&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;S.B.S. College of Pharmacy, Patti, Tarn Taran, Punjab, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Pharmaceutical Sciences, IKG Punjab Technical University, Punjab, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;PG Department of Chemistry, Khalsa College Amritsar, Punjab, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sanjay Kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chromosomal Disturbances during Mitotic Activity of Root Tip Cells in Allium by Certain Commonly Used Antibiotics</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Allium cepa</style></keyword><keyword><style  face="normal" font="default" size="100%">Antibiotics</style></keyword><keyword><style  face="normal" font="default" size="100%">Chromosomal disturbances</style></keyword><keyword><style  face="normal" font="default" size="100%">Clastogenic abnormalities</style></keyword><keyword><style  face="normal" font="default" size="100%">Physiological disturbances</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/490</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">355-365</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The certain commonly used antibiotics (cefixime, metronidazole, ciprofloxacin, cefpodoxime and cetirizine) purchased from the chemist shop in Mokokchung town, Nagaland and effects on mitotic activity of root tip meristematic cells of &lt;em&gt;Allium Cepa&lt;/em&gt; were observed. &lt;strong&gt;Methods:&lt;/strong&gt; The different concentrations were prepared by retaining the original effective concentrations (400, 400, 500, 200 and 10 mg) of the antibiotics and treated the root tips of &lt;em&gt;Allium&lt;/em&gt; at different times (6, 12 and 24 h) to record the effects or abnormalities. &lt;strong&gt;Results:&lt;/strong&gt; All the concentrations (ppm) and time (h) were effective to induce the chromosomal disturbances during the mitotic activity of root tip cells in &lt;em&gt;Allium&lt;/em&gt;. &lt;strong&gt;Conclusion:&lt;/strong&gt; The mean value (&amp;plusmn;S.E.) recorded for mitotic cells, mitotic stages, physiological and clastogenic abnormalities and showed a mixed response which could not predict dose response curve in actual.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">355</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Sanjay Kumar &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Botany, Banaras Hindu University, Varanasi-221005, Uttar Pradesh, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Serebryanaya Fatima Kazbekovna</style></author><author><style face="normal" font="default" size="100%">Orlov Aleksei Nikolaevich</style></author><author><style face="normal" font="default" size="100%">Konovalov Dmitryi Alexeevich</style></author><author><style face="normal" font="default" size="100%">Naida Mahmudovna Nasuhova</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Morphological and Anatomical Research of Leaves 6 Sorts of Laurels Noble (Laurus Nobilis L.), Growing in the Conditions of an Introduction in the Nikitsky Botanical Garden</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anatomical topographical schemes</style></keyword><keyword><style  face="normal" font="default" size="100%">Comparative micromorphological study</style></keyword><keyword><style  face="normal" font="default" size="100%">Cross-section of leaf and petiole</style></keyword><keyword><style  face="normal" font="default" size="100%">Laurus Nobilis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/415</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">172-178</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;This research is a fragment of complex studying of grades of laurels of the noble, growing in the territory of botanical gardens of Pyatigorsk medical and pharmaceutical institute and the Nikitsky botanical garden which is carried out based on department of botany and a pharmacognosy of the Pyatigorsk medical and pharmaceutical institute. &lt;strong&gt;Introduction:&lt;/strong&gt; Research objective is to conduct a comparative morphological and anatomical research of leaves of 6 sorts of Laurus nobilis. &lt;strong&gt;Material and Methods:&lt;/strong&gt; The exemplars of leaves of 6 grades of laurels noble, growing in the territory of the Nikitsky botanical garden (the settlement of Nikita, Crimea republic). When carrying out comparative morphometric, micromorphological, histochemical methods. &lt;strong&gt;Results:&lt;/strong&gt; The comparative morphometric research of a leaf plate is conducted, at the same time the form of a leaf plate, character of a top, basis and margined of a leaf plate were estimated. In the analysis of features of a micromorphological structure carried out the analysis of an anatomic structure of scapes of leaves and a structure of a transversal cut of a sheet plate, a top and bottom epidermal of a sheet plate. The form of the cross- section of the petiole is horseshoe-shaped, dredging is absent or falciform with the expressed dredging, rounded triangular form, dredging is absent. The presence or absence of coverage trichomes, the presence only at the top party of a scape and it is presented by individual monocelled lengthiest hairs, is presented by a small amount of individual, monocelled small hairs on the top party of a petiole it is presented by individual monocelled small hairs. Existence and arrangement of a resin ducts are presented in big quantity, especially there is a lot of around a phloem part of a vascular bundle or the ducts are presented in a great many, there is a lot of them, both around a phloem part of a vascular bundle, and under epidermis. Existence and arrangement of a sclerenchyme &amp;ndash;around the vascular bundle from two parties or it is presented by groups of fibers around the vascular bundle or absent. &lt;strong&gt;Conclusion:&lt;/strong&gt; As for an anatomic structure of an epidermis of a leaf plate, differences in a histological structure of an epidermis of the studied grades of laurels noble it is not revealed. The following signs are characteristic of all studied exemplars: leaf plate of hypostomatic type. Stomates are present only at the lower part of an epidermis. The stomatal type is anomocytic. Epidermal cages of the lower epidermis have the extended form with sinuous anticlinal walls. Anticlinal walls of the main cages of the top epidermis have the reference uniform thickenings In the analysis of features of a micromorphological structure carried out the analysis of an anatomic structure of scapes of leaves and a structure of a transversal cut of a sheet plate, a top and bottom epidermal of a sheet plate.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">172</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Serebryanaya Fatima Ka-zbekovna&lt;sup&gt;1,2&lt;/sup&gt;, Orlov Aleksei Nikolaevich&lt;sup&gt;1&lt;/sup&gt;, Konovalov Dmitryi Alexeevich&lt;sup&gt;1&lt;/sup&gt;, Naida Mahmudovna Nasuhova&lt;sup&gt;1 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy and Botany, Pyatigorsk Medical and Pharmaceutical Institute, a branch of Volgograd State Medical University Ministry of Health of the Russian Federation, Pyatigorsk, 357532, Kalinina av.11, RUSSIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Ecological and botanical station Pyatigorsk of Botanical institute of Russian Academy of sciences, 197376, Saint-Petersburg, Prof. Popova av. 2, RUSSIA.&amp;nbsp;&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ghazi Faisal Najmuldeen</style></author><author><style face="normal" font="default" size="100%">Kamalanathan  Narayanan</style></author><author><style face="normal" font="default" size="100%">Deeveeya A/P Kirubananthan</style></author><author><style face="normal" font="default" size="100%">Ghasak Ghazi Faisal</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparison of Tongkat Ali Root Chemical Composition Extracted by Soxhlet, Conventional Steam and Microwave Assisted Extraction Techniques</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Conventional Steam Extraction (CSE)</style></keyword><keyword><style  face="normal" font="default" size="100%">Essential oil</style></keyword><keyword><style  face="normal" font="default" size="100%">Eurycoma longifolia Jack</style></keyword><keyword><style  face="normal" font="default" size="100%">Microwave assisted extraction</style></keyword><keyword><style  face="normal" font="default" size="100%">Soxhlet Extraction</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">916-920</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Eurycoma longifolia Jack (Tongkat Ali) roots are used in traditional medicines for its wide range of biological effects. The process of extracting out this essential oil from the plant requires a delicate and efficient method. In this research the extract of the essential oil of &lt;em&gt;Eurycoma longifolia&amp;rsquo;s&lt;/em&gt; root using Microwave Assisted Extraction (MAE), Soxhlet Extraction and Conventional Steam Extraction (CSE) methods, is characterized to identify the components of essential oil extracted and then to compare the yield percentage and components of the extracts from both methods. The extract obtained was characterized using gas chromatography mass spectroscopy (GC-MS) by comparing the compositions of components present in commercial Tongkat Ali oil stored in the GC-MS library. The findings showed that the MAE gives a maximum yield percentage of 5% with six chemical components extracted in 20 min while SE and CSE gives high yield percentage of 28.3% in 3 h and 2.5 % in 6 h respectively with only three chemical components extracted. Therefore, MAE is the optimum method for extracting essential oil from Tongkat Ali with a high quality.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">916</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Ghazi Faisal Najmuldeen&lt;sup&gt;1&lt;/sup&gt;, Kamalanathan  Narayanan&lt;sup&gt;1&lt;/sup&gt;, Deeveeya A/P Kirubananthan&lt;sup&gt;1&lt;/sup&gt;, Ghasak Ghazi Faisal&lt;sup&gt;2&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Chemical and Natural Resources Engineering, University Malaysia Pahang, 26300 Gambang, Pahang, MALAYSIA.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt; 2&lt;/sup&gt;Department of Fundamental Dental and Medical Sciences, Kulliyya of Dentistry, International Islamic University, MALAYSIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ramdan Btissam</style></author><author><style face="normal" font="default" size="100%">El Malki Fatima</style></author><author><style face="normal" font="default" size="100%">Eddarraji Kamal</style></author><author><style face="normal" font="default" size="100%">Greche Hassane</style></author><author><style face="normal" font="default" size="100%">NHIRI Mohamed</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Composition and Antibacterial Activity of Hydro-Alcohol and Aqueous Extracts Obtained from the Lamiaceae Family</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Aqueous Extract.</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoic Content</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydro-Alcohol Extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Lamiaceae Family</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolic compounds</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/402</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">81-91</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Context:&lt;/strong&gt; Plant from the &lt;em&gt;Lamiaceae&lt;/em&gt; family are considered as dietary spices and medicinal herbs traditionally used in medicine for the treatment of several pathologies. &lt;strong&gt;Objective:&lt;/strong&gt; Evaluation of the &lt;em&gt;in vitro&lt;/em&gt; antibacterial activity of ethanol and aqueous extracts of nine Moroccan plants from the Lamiaceae family against six bacterial strains regularly implicated in toxiinfection. &lt;strong&gt;Method:&lt;/strong&gt; The antibacterial activities of hot (HAE), cold (CAE) aqueous extracts and ethanolic extracts (EE) were evaluated using agar-well diffusion method, minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) and IC&lt;sub&gt;50&lt;/sub&gt; against six foodborne bacteria (&lt;em&gt;Bacillus cereus, Listeria monocytogenes, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa&lt;/em&gt; and &lt;em&gt;Salmonella enterica&lt;/em&gt;). Total phenolic and flavonoid contents were assessed as well. &lt;strong&gt;Results:&lt;/strong&gt; In the present study, the ethanol extracts were rich in polyphenols, with middling values of flavonoids, and relatively poor in condensed tannins. The presence of saponins, essential oils, irroides, alkaloids, anthocyanins, and aldehydes was recorded. The effect of the extracts was directly bactericidal for &lt;em&gt;B. cereus&lt;/em&gt; and &lt;em&gt;L. monocytogenes&lt;/em&gt;; for the other strains, the MBC value was twice higher than that of MIC. However, the ethanol extract (EE) of &lt;em&gt;O. majorana&lt;/em&gt; and &lt;em&gt;T. satureioides &lt;/em&gt;showed the highest antibacterial activity. With the principal component analysis, it was demonstrated that the nine &lt;em&gt;Lamiaceae&lt;/em&gt; family plants possess a powerful antibacterial effect, correlated with their phenolic content. &lt;strong&gt;Statistical analysis:&lt;/strong&gt; Analysis of variance was performed by uni-varied ANOVA in the software SPSS 22 Fr. &lt;strong&gt;Conclusion:&lt;/strong&gt; The active compounds were thermostable and soluble in ethanol and water. The antimicrobial activities of the plants extracts investigated may contribute to understand their involvement in traditional medicine against many microbial infections.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">81</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Ramdan Btissam&lt;sup&gt;1&lt;/sup&gt;, El Malki Fatima&lt;sup&gt;2&lt;/sup&gt;, Eddarraji Kamal&lt;sup&gt;1,2&lt;/sup&gt;, Greche Hassane&lt;sup&gt;3&lt;/sup&gt; and Nhiri Mohamed&lt;sup&gt;1&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;sup&gt; 1&lt;/sup&gt;Department of Biology, Laboratory of Biochemistry and Molecular Genetics, Faculty of Science and Technology, University Abdelmalek Essaadi, BP 416, Tangier 90000, MOROCCO.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Laboratory of Microbiology, Department of Hygiene and Food Safety, Pasteur Institute of Morocco, Tangier 90000, MOROCCO.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;National Institute of Medicinal and Aromatic Plants, University of Sidi Mohamed Ben Abdellah, BP 8857, 30100 Atlas, Fes, MOROCCO.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ampa Konsue</style></author><author><style face="normal" font="default" size="100%">Chusri Talubmook</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Thai Folklore Recipe from Abutilon indicum and Mimosa pudica in Streptozotocin-Induced Diabetic Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">A. indicum</style></keyword><keyword><style  face="normal" font="default" size="100%">Fasting blood glucose</style></keyword><keyword><style  face="normal" font="default" size="100%">M. pudica</style></keyword><keyword><style  face="normal" font="default" size="100%">Thai folklore recipe</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/512</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">480-485</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Context:&lt;/strong&gt; &lt;em&gt;Abutilon indicum&lt;/em&gt; and &lt;em&gt;Mimosa pudica&lt;/em&gt; were a folklore recipe in Northeastern of Thailand. The recipe was reported that claim to diabetic treatment. &lt;strong&gt;Aims:&lt;/strong&gt; The studies were evaluated to hypoglycemic effect, serum insulin secretion and blood biochemistry in streptozotocin (STZ)-induced diabetic rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The recipe were composed of whole plants from &lt;em&gt;A. indicum&lt;/em&gt; and &lt;em&gt;M. Pudica&lt;/em&gt; (1:1 w/w) powder. The pound plants were macerated with aqueous (AMA), hydro-ethanol (AMHE) and 80% ethanol (AME) to crude extracts. The AMA, AMHE and AME at the doses of 125, 250 and 500 mg/kg body weight (b.w.) were administered orally daily in diabetic rats during eight weeks. Fasting blood glucose levels (FBG) were measured at weekly. The serum insulin levels and blood biochemical data including blood urea nitrogen (BUN), creatinine (CREA), total protein (TP), albumin (Alb), serum aspartate aminotransferase (AST), serum alanine aminotransferase (ALT), alkaline phosphatase (ALP), triglycerides (TG), total cholesterol (TC), high-density lipoprotein (HDL) and low-density lipoprotein (LDL) were estimated at the end of experiment. &lt;strong&gt;Results:&lt;/strong&gt; All doses of the extracts were showed significantly (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05) decreasing percent age of FBG in diabetic rats. Especially, AME 125 mg/ kg b.w. was showed more potent significantly (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05) decreasing percentage of FBG at week of 2, 5, 7 and 8. The serum insulin levels of all doses administered with the extracts were significantly (&lt;em&gt;p&lt;/em&gt;&amp;lt; 0.05) higher than diabetic control group. On the other hand, all doses of the extracts were significantly (&lt;em&gt;p&lt;/em&gt;&amp;lt; 0.05) decreasing ALT and ALP lower than diabetic control group. While, AMA and AMHE at the doses of 250 and 500 mg/kg b.w. were increased HDL, but decreased TC, TG and LDL. &lt;strong&gt;Conclusion:&lt;/strong&gt; The study was proved to diabetic treatment and improvement of diabetic stage and blood biochemical parameters. In addition, the experiment was confirmed to folklore traditional use.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">480</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Ampa Konsue&lt;sup&gt;1*&lt;/sup&gt;, Chusri Talubmook&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Medicine, Mahasarakham University, Maha Sarakham, THAILAND.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biology, Faculty of Sciences, Mahasarakham University, Maha Sarakham, THAILAND.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ampa Konsue</style></author><author><style face="normal" font="default" size="100%">Chusri Talubmook</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Thai Folklore Recipe from Abutilon indicum and Mimosa pudica in Streptozotocin-Induced Diabetic Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">A. indicum</style></keyword><keyword><style  face="normal" font="default" size="100%">Fasting blood glucose.</style></keyword><keyword><style  face="normal" font="default" size="100%">M. pudica</style></keyword><keyword><style  face="normal" font="default" size="100%">Thai folklore recipe</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">x</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">x</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Context:&lt;/strong&gt; &lt;em&gt;Abutilon indicum&lt;/em&gt; and &lt;em&gt;Mimosa pudica&lt;/em&gt; were a folklore recipe in Northeastern of Thailand. The recipe was reported that claim to diabetic treatment. &lt;strong&gt;Aims:&lt;/strong&gt; The studies were evaluated to hypoglycemic effect, serum insulin secretion and blood biochemistry in streptozotocin (STZ)-induced diabetic rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The recipe were composed of whole plants from &lt;em&gt;A. indicum&lt;/em&gt; and &lt;em&gt;M. Pudica&lt;/em&gt; (1:1 w/w) powder. The pound plants were macerated with aqueous (AMA), hydro-ethanol (AMHE) and 80% ethanol (AME) to crude extracts. The AMA, AMHE and AME at the doses of 125, 250 and 500 mg/kg body weight (b.w.) were administered orally daily in diabetic rats during eight weeks. Fasting blood glucose levels (FBG) were measured at weekly. The serum insulin levels and blood biochemical data including blood urea nitrogen (BUN), creatinine (CREA), total protein (TP), albumin (Alb), serum aspartate aminotransferase (AST), serum alanine aminotransferase (ALT), alkaline phosphatase (ALP), triglycerides (TG), total cholesterol (TC), high-density lipoprotein (HDL) and low-density lipoprotein (LDL) were estimated at the end of experiment. &lt;strong&gt;Results:&lt;/strong&gt; All doses of the extracts were showed significantly (p&amp;lt;0.05) decreasing percent age of FBG in diabetic rats. Especially, AME 125 mg/ kg b.w. was showed more potent significantly (p&amp;lt;0.05) decreasing percentage of FBG at week of 2, 5, 7 and 8. The serum insulin levels of all doses administered with the extracts were significantly (&lt;em&gt;p&lt;/em&gt;&amp;lt; 0.05) higher than diabetic control group. On the other hand, all doses of the extracts were significantly (p&amp;lt; 0.05) decreasing ALT and ALP lower than diabetic control group. While, AMA and AMHE at the doses of 250 and 500 mg/kg b.w. were increased HDL, but decreased TC, TG and LDL. &lt;strong&gt;Conclusion:&lt;/strong&gt; The study was proved to diabetic treatment and improvement of diabetic stage and blood biochemical parameters. In addition, the experiment was confirmed to folklore traditional use.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Thai folklore recipe, A. indicum , M. pudica , Fasting blood glucose.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2s</style></issue><work-type><style face="normal" font="default" size="100%">x</style></work-type><section><style face="normal" font="default" size="100%">x</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ampa Konsue&lt;sup&gt;1*&lt;/sup&gt;, Chusri Talubmook&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Medicine, Mahasarakham University, Maha Sarakham, THAILAND.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biology, Faculty of Sciences, Mahasarakham University, Maha Sarakham, THAILAND.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Marni Karo</style></author><author><style face="normal" font="default" size="100%">Mochammad Hatta</style></author><author><style face="normal" font="default" size="100%">WaOde Salma</style></author><author><style face="normal" font="default" size="100%">Ilhamjaya Patellongi</style></author><author><style face="normal" font="default" size="100%">Rosdiana Natzir</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effects of Miana (Coleus scutellariodes (L) Benth) to Expression of mRNA IL-37 in Balb/c Mice Infected Candida albicans</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">CFU</style></keyword><keyword><style  face="normal" font="default" size="100%">Interleukin-37 mRNA</style></keyword><keyword><style  face="normal" font="default" size="100%">Miana</style></keyword><keyword><style  face="normal" font="default" size="100%">Realtime PCR</style></keyword><keyword><style  face="normal" font="default" size="100%">Vulvovaginal Candidiasis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/358</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">16-19</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Miana (&lt;em&gt;Coleus scutellariodes&lt;/em&gt; (L) Benth) are a herbal medicine with potential anti-inflammatory properties in patients infected with vulvovaginal candidiasis. The objective of this work was to the analyze IL-37 expression following administration of miana leaf extract (MLE) in an animal model of vulvovaginal candidiasis. &lt;strong&gt;Material and Methods:&lt;/strong&gt; Adult Balb/c mice, aged 8&amp;ndash;12 weeks and weighing 30&amp;ndash;40 g, were divided into five groups. Four groups were administered &lt;em&gt;Candida albicans&lt;/em&gt; via intravaginal inoculation with a diluted dose of 10&lt;sup&gt;-2&lt;/sup&gt;/ ml and were treated with either MLE, a placebo, or ketoconazole; one group constituted the healthy control and was only treated with MLE. Real-time PCR was used to measure the expression of IL-37. &lt;strong&gt;Results:&lt;/strong&gt; These findings indicated that a component within MLE may mediate its anti-inflammatory characteristics, as indicated by the increase in mRNA IL-37 expression in mice inoculated with &lt;em&gt;C. albicans&lt;/em&gt;. The highest increase in fungal load to 101.6 CFU was observed in the placebo group at day 14. Whereas for the mice treated with MLE at 750 mg/kg b.w, the fungal load only increased to 30.0 CFU, similar to that of mice treated with ketoconazole (29.6 CFU). In the mice treated with MLE at 500 mg/kg b.w, the fungal load increased to 68.2 CFU. &lt;strong&gt;Conclusion:&lt;/strong&gt;&amp;nbsp;Fungiostatic effect of MLE 750 mg/kg BB is not less than ketoconazole and MLE may act as anti-inflammatory throught its role as an antioxidant so it could potentially be used as an alternative treatment in humans especially patients with vulvovaginal candidiasis.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">16</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Marni Karo&lt;sup&gt;1&lt;/sup&gt;, Mochammad Hatta&lt;sup&gt;2&lt;/sup&gt;*, WaOde Salma&lt;sup&gt;3&lt;/sup&gt;, Ilhamjaya Patellongi&lt;sup&gt;4&lt;/sup&gt;, Rosdiana Natzir&lt;sup&gt;5&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Midwifey Program of Medistra Health Higher School, Jakarta. Indonesia andSchool of Post Graduate Faculty of Medicine, Hasanuddin University, Makassar, INDONESIA.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Molecular Biology and Immunology Laboratory for Infection Diseases, Faculty of Medicine, Hasanuddin University, Makassar, INDONESIA.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt; 3&lt;/sup&gt;Department Nutrition, Faculty of Medicine, Halu Oleo University, Kendari, INDONESIA.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biostatistic, Faculty of Medicine, Hasanuddin University, Makassar, INDONESIA.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Biochemistry Faculty of Medicine, Hasanuddin University, Makassar, INDONESIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tetiana Derkach</style></author><author><style face="normal" font="default" size="100%">Volodymyr Khomenko</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Elemental Composition of the Medicinal Plants Hypericum perforatum, Urtica dioica and Matricaria chamomilla Grown in Ukraine: A Comparative Study</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Atomic absorption spectroscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">Cd contamination</style></keyword><keyword><style  face="normal" font="default" size="100%">Elemental composition</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal plants</style></keyword><keyword><style  face="normal" font="default" size="100%">Pb</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/513</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">486-491</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; To determine concentrations of essential microelements Fe, Cu, Mn and Zn, as well as toxic metals Pb, Cd, Cr and Co, in three herbal remedies and compare the experimental data obtained with available literature data. Materials and &lt;strong&gt;Methods:&lt;/strong&gt; Elemental compositions of three herbal remedies, Chamomile flowers, Urtica folia (nettle) and Hyperichi herba (St John&amp;rsquo;s wort), grown and produced in Ukraine, were studied by flame atomic absorption spectroscopy. &lt;strong&gt;Results:&lt;/strong&gt; The Fe concentration decreases, as well as the Zn and Mn concentrations, increase in going from nettle through chamomile to St John&amp;rsquo;s wort. The Cu content is virtually independent of the plant type. Statistically significant negative correlations between the element concentrations were found in Fe-Mn and Fe-Zn pairs. The studied samples of St John&amp;rsquo;s wort are more contaminated with Cd than other plants, while the highest Pb content is observed in some samples of nettle. &lt;strong&gt;Conclusion:&lt;/strong&gt; The measured levels of both Pb and Cd still secure against overuse of toxic metals with herbal remedies.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Medicinal plants, Atomic absorption spectroscopy, Elemental composition, Pb, Cd contamination.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">486</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Tetiana Derkach&lt;sup&gt;1*&lt;/sup&gt;, Volodymyr Khomenko&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Industrial Pharmacy, Kyiv National University of Technologies and Design, Nemyrovicha-Danchenko Str. 2, Kyiv, 01011, UKRAINE.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Electrochemical Energetics and Chemistry, Kyiv National University of Technologies and Design, Nemyrovicha-Danchenko Str. 2, Kyiv, 01011, UKRAINE.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Victoria Vladimirovna Fedotova</style></author><author><style face="normal" font="default" size="100%">Dmitry Alexeevich Konovalov</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Essential Oil and Anatomical Study of Flowers Solidago caucasica Kem.-Nath.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chromoplasts</style></keyword><keyword><style  face="normal" font="default" size="100%">Humulene epoxide</style></keyword><keyword><style  face="normal" font="default" size="100%">Pathulenol</style></keyword><keyword><style  face="normal" font="default" size="100%">Solidago caucasica Kem.-Nath.</style></keyword><keyword><style  face="normal" font="default" size="100%">Trichomes</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">s63-s65</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Plant &lt;em&gt;Solidago caucasica&lt;/em&gt; Kem.-Nath. (Asteraceae) is studied by us for the first time. We have established its diuretic and antimicrobial action. The study of essential oil and the anatomical structure of &lt;em&gt;S. caucasica&lt;/em&gt; flowers is presented for the first time in this article.&lt;strong&gt; Materials and Methods:&lt;/strong&gt; &lt;em&gt;S. caucasica&lt;/em&gt; flowers were collected at the beginning of flowering in the botanical garden of the Pyatigorsk Medical and Pharmaceutical Institute. Essential oil was obtained by hydro distillation. The component composition of the essential oil was studied by liquid chromatography&amp;ndash;mass spectrometry. Results: The main components of essential oil and microscopic diagnostic signs of &lt;em&gt;S. caucasica&lt;/em&gt; flowers were established. &lt;em&gt;Solidago&lt;/em&gt; &lt;em&gt;caucasica&lt;/em&gt; flowers contain 0.57% essential oil. It contains humulene epoxide H (-)-spathulenol, &amp;beta;-linalool, &amp;alpha;-terpinol, trans-geraniol, carvacrol and others. Numerous pappus hairs meet in the microscopy of the flower. Ligulate florets are characterized by round chromoplasts, covering trichomes multicellular. Epidermal cells of the tubular florets have polygonal chromoplasts, trichomes, consisting of several cells fused with each other, covering trichomes with a thick wall and a thin cavity inside. On the epidermis of the involucre there are stomata of anomocytic type, glandular trichomes, trichomes cone-shaped, trichomes wide and essential oil glands. &lt;strong&gt;Conclusion:&lt;/strong&gt; The obtained standards will provide referential information for correct identification, purity, standardization and preparation of monograph of&lt;em&gt; S. caucasica&lt;/em&gt;.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s63</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Victoria Vladimirovna Fedotova, Dmitry Alexeevich Konovalov&lt;sup&gt;* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Pharmacognosy and Botany, Pyatigorsk Medical and Pharmaceutical Institute, A Branch of Volgograd State Medical University, Ministry of Health of Russian Federation, Pyatigorsk, 357532, Kalinina 11, RUSSIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohd Saidur Rahman</style></author><author><style face="normal" font="default" size="100%">Md. Mujahid</style></author><author><style face="normal" font="default" size="100%">Mohd Aftab Siddiqui</style></author><author><style face="normal" font="default" size="100%">Md. Azizur Rahman,</style></author><author><style face="normal" font="default" size="100%">Muhammad Arif</style></author><author><style face="normal" font="default" size="100%">Shimaila Eram</style></author><author><style face="normal" font="default" size="100%">Anayatullah Khan</style></author><author><style face="normal" font="default" size="100%">Md Azeemuddin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ethnobotanical Uses, Phytochemistry and Pharmacological Activities of Pterocarpus marsupium: A Review</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antidiabetic</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Epicatechin</style></keyword><keyword><style  face="normal" font="default" size="100%">Indian Kino</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacology</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">Pterocarpus marsupium</style></keyword><keyword><style  face="normal" font="default" size="100%">Tannin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">s1-s8</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;em&gt;Pterocarpus marsupium&lt;/em&gt; is an important therapeutic and medicinal plant belonging to family Fabaceae and commonly named as Indian Kino tree, Bijasal, Venga or Vijayasara. It is a huge deciduous plant and widely distributed in the Central, Western and Southern regions of India. Role of&lt;em&gt; P. marsupium&lt;/em&gt; is found in Ayurveda, Homeopathic and Unani systems of medicine. It is a decent source of tannins and flavonoids hence, used as influential astringent, anodyne, cooling, regenerating agent and also used for the treatments of leprosy, leucoderma, toothache, fractures, diarrhea, passive hemorrhage, and dysentery, bruises and diabetes. It is also used to treat rheumatoid arthritis, gout, diabetic anemia, indigestion, asthma, cough, discoloration of hair, bronchitis, ophthalmic complications, elephantiasis and erysipelas. Researchers have been stated the presence of several phytoconstituents in &lt;em&gt;P. marsupium&lt;/em&gt; and also their pharmacological activities. The current review aimed to define the phytochemical and pharmacological aspects of &lt;em&gt;P. marsupium&lt;/em&gt; which will have been help in the researchers for further qualitative research.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">s1</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Mohd SaidurRahman, Md. Mujahid&lt;sup&gt;*&lt;/sup&gt;, Mohd Aftab Siddiqui, Md. Azizur Rahman, Muhammad Arif, Shimaila Eram, Anayatullah Khan, Md Azeemuddin&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;Department of Pharmacy, Herbal Bioactive Research Laboratory, Faculty of Pharmacy, Integral University, Lucknow, Uttar Pradesh -226026, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lubna Azmi</style></author><author><style face="normal" font="default" size="100%">Ila Shukla</style></author><author><style face="normal" font="default" size="100%">Shyam Sundar Gupta</style></author><author><style face="normal" font="default" size="100%">Aniruddh Chaudhary</style></author><author><style face="normal" font="default" size="100%">Padam Kant</style></author><author><style face="normal" font="default" size="100%">Narayan Prasad Yadav</style></author><author><style face="normal" font="default" size="100%">Chandana Venkateswara Rao</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Chemoprotective Effect of Quercetin from Argyreia speciosa against N-methyl-N-Nitro-N-Nitrosoguanidine and NaCl-Induced Gastric Carcinomas in Wistar Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Argyreia speciosa</style></keyword><keyword><style  face="normal" font="default" size="100%">Gastric carcinoma</style></keyword><keyword><style  face="normal" font="default" size="100%">Immunochemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercetin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/467</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">215-220</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objectives:&lt;/strong&gt; This study was carried out to investigate the chemo protective potential of Quercetin, an isolated compound from &lt;em&gt;Argyreia speciosa&lt;/em&gt;, on N-methyl-N-nitro-N-nitrosoguanidine and NaCl-induced gastric carcinomas in Wistar rats. &lt;strong&gt;Methods:&lt;/strong&gt; The rats were fed with a diet supplemented with 8% NaCl and simultaneously given N-methyl-N-nitro-N-nitrosoguanidine. After administration of the carcinogen, quercetin was administered. The whole stomach and a part of duodenum were sampled, cut open and tumors were recorded. The specimens were histopathologically investigated and the expression of surviving was examined with immunohistochemical analysis.&lt;strong&gt; Results and Conclusions:&lt;/strong&gt; The treatment with quercetin significantly increases body weight in the rats after N-methyl-N-nitro-N-nitrosoguanidine administration. Survivin expression in glandular stomachs of normal rats, of rats in adenocarcinomas and quercetin at dose dependent manner treated rats were 0%, 90%, 75%, 33.3-25%, respectively. Compared with the survivin expression in negative rats, the differences were significant. Compared with the survivin expression in normal rats, the differences were significant. Histological observations of stomach tissues too correlated with the biochemical observations. These findings indicated that the Quercetin treatment could stimulate immunity activity in rats with N-methyl-N-nitro-N-nitrosoguanidine induced gastric carcinoma and have pronounced effect on survivin which is an attractive target for gastric cancer therapy.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">215</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Lubna Azmi &lt;sup&gt;1,2&lt;/sup&gt;, Ila Shukla&lt;sup&gt;1&lt;/sup&gt;, Shyam Sundar Gupta&lt;sup&gt;1&lt;/sup&gt;, Aniruddh Chaudhary&lt;sup&gt;2&lt;/sup&gt;, Padam Kant&lt;sup&gt;2&lt;/sup&gt;, Narayan Prasad Yadav&lt;sup&gt;3&lt;/sup&gt;, Chandana Venkateswara Rao&lt;sup&gt;1* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Pharmacognosy and Ethnopharmacology Division, CSIR-National Botanical Research Institute, Lucknow, Uttar Pradesh, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemistry, University of Lucknow, Lucknow, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Botany and Pharmacognosy Department, CSIR-Central Institute of Medicinal and Aromatic Plants, P.O. CIMAP, Lucknow, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lorina Ineta Badger-Emeka</style></author><author><style face="normal" font="default" size="100%">Hany Ezzat Khalil</style></author><author><style face="normal" font="default" size="100%">Promise Madu Emeka</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Different Fractions of Garcinia kola Extracts against Multidrug Resistant Clinical Bacterial and Fungal Isolates</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Clinical isolates</style></keyword><keyword><style  face="normal" font="default" size="100%">Garcinia kola</style></keyword><keyword><style  face="normal" font="default" size="100%">Minimum inhibitory concentration</style></keyword><keyword><style  face="normal" font="default" size="100%">Multidrug resistant bacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">Sensitivity</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">1055-1060</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; The effectiveness of antibiotics used in the treatment of bacterial infections has been on the decline due to bacterial resistance. To improve clinical management of recalcitrant bacterial infections, alternative therapy such as medicinal plant products are now being evaluated. This study investigates the antimicrobial effects of &lt;em&gt;Garcinia kola&lt;/em&gt; fractions on clinical isolates of multidrug resistant gram negative bacteria and Candida. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; &lt;em&gt;Escherichia coli&amp;nbsp;&lt;/em&gt;, &lt;em&gt;Acinetobacter baumannii&lt;/em&gt;, &lt;em&gt;Serratia marcescens&lt;/em&gt; and &lt;em&gt;Candida species&lt;/em&gt; were used for the study. Microbial isolation and antimicrobial susceptibility test was carried out using basic microbiological procedures. Confirmation of all isolates was done using the VITEK 2 compact automated system (BioMerieux, Marcy I&amp;rsquo;Etoile France). The powdered dried seeds of&lt;em&gt; G. kola&lt;/em&gt; were extracted with 70% methanol for 7 days, using a cold maceration method. The crude extracts were evaporated to dryness, using different solvents to obtain the fractions according to standard fractionation techniques. &lt;strong&gt;Results:&lt;/strong&gt; The aqueous, butanol, chloroform and hexane fractions at minimum inhibitory concentrations (MIC) of 25mg/ml were active against &lt;em&gt;A. baumannii&lt;/em&gt;. Ethyl acetate fraction at MIC of 20 mg/ml also produced growth inhibition of same isolates. At the same MICs, the different fractions were observed to inhibit the growth of candida albicans (CF1) isolate. Overall, aqueous fraction of &lt;em&gt;G. kola&lt;/em&gt; produced more growth inhibition followed by butanol fractions, with chloroform fractions producing the least effects. &lt;strong&gt;Conclusion:&lt;/strong&gt; The antibacterial potencies of these extracts could be useful for the treatment of multi-drug-resistant&lt;em&gt; A. baumannii&lt;/em&gt;. The aqueous fraction showed better activities than the other fractions studied.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1055</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Lorina Ineta Badger-Emeka&lt;sup&gt;1&lt;/sup&gt;*, Hany Ezzat Khalil&lt;sup&gt;2&lt;/sup&gt;, Promise Madu Emeka&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biomedical Sciences, College of Medicine, King Faisal University. Al-Ahsa, KINGDOM OF SAUDI ARABIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa, KINGDOM OF SAUDI ARABIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sachin Annasaheb Nitave</style></author><author><style face="normal" font="default" size="100%">Nilesh B. Chougule</style></author><author><style face="normal" font="default" size="100%">Kailasam Koumaravelou</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Formulation and Evaluation of Solid Dispersion Tablet of Andrographis paniculata Extract</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Andrographis paniculata</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethanolic extract</style></keyword><keyword><style  face="normal" font="default" size="100%">PEG 6000</style></keyword><keyword><style  face="normal" font="default" size="100%">Solid dispersion</style></keyword><keyword><style  face="normal" font="default" size="100%">Soluplus</style></keyword><keyword><style  face="normal" font="default" size="100%">Solvent evaporation technique</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">1047-1054</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; To enhance solubility of ethanolic extract of &lt;em&gt;Andrographis paniculata&lt;/em&gt; by solid dispersion technique and to perform formulation and evaluation of solid dispersion tablet. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Solid dispersion of &lt;em&gt;Andrographis paniculata&lt;/em&gt; extract has been prepared by solvent evaporation technique using soluplus and PEG 6000. Prepared solid dispersions have been evaluated for various micromeritic properties. The tablets of solid dispersion were prepared by direct compression technique and were evaluated for various physical tests and&lt;em&gt; in-vitro&lt;/em&gt; dissolution study. &lt;strong&gt;Results:&lt;/strong&gt; The study showed that prepared solid dispersion has good flow property and compressibility. The solubility of extract was found to be more from solid dispersion prepared by using soluplus than that of prepared by using PEG 6000. The rate of drug release was found to be higher in acidic buffer at pH 1.2 as compared to that of in phosphate buffer at pH 6.8. &lt;strong&gt;Conclusion:&lt;/strong&gt; The study concludes that the solid dispersion tablet of ethanolic extract of &lt;em&gt;Andrographis paniculata&lt;/em&gt; can be effectively prepared using soluplus by solvent evaporation techniqu&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1047</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Sachin Annasaheb Nitave&lt;sup&gt;1,2&lt;/sup&gt;*, Nilesh B. Chougule&lt;sup&gt;1,3&lt;/sup&gt;, Kailasam Koumaravelou&lt;sup&gt;4&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Research Scholar, Centre for Research and Development, PRIST University, Vallam, Thanjavur, 613 403, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Principal, Dr. J. J. Magdum Trust&amp;rsquo;s Anil alias Pintu Magdum Memorial Pharmacy College Dharangutti, 416101, Shirol, Kolhapur, Maharashtra, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Principal, Annasaheb Dange College of Pharmacy, Ashta, Sangli, Maharashtra, INDIA. 4Director, PRIST University, Puducherry Campus, 605007, Puducherry, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Somanjana Khatua</style></author><author><style face="normal" font="default" size="100%">Krishnendu Acharya</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Functional Ingredients and Medicinal Prospects of Ethanol Extract from Macrocybe lobayensis</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant potential</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethanol Extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Wild edible mushroom</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">1154-1158</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Mushrooms are a good source of bioactive components and have been traditionally consumed across the globe for maintaining health. However, information concerning medicinal activity of ethnically popular macrofungi still remains limited. &lt;strong&gt;Aim:&lt;/strong&gt; Therefore, the present study was aimed for determination of functional constituents and therapeutic efficacy of a less explored mushroom, &lt;em&gt;Macrocybe lobayensis&lt;/em&gt; that has been habitually used in local diets. &lt;strong&gt;Method:&lt;/strong&gt; In this context, an ethanol extract was prepared from dried basidiocarps and characterized by spectrophotometry and HPLC to identify bioactive constituents. Alongside, the fraction was also subjected for evaluation of medicinal properties namely antioxidant and antibacterial effects. &lt;strong&gt;Results:&lt;/strong&gt; The formulation was found to be consisted mainly of phenolic compounds (pyrogallol&amp;gt; cinnamic acid&amp;gt; &lt;em&gt;p&lt;/em&gt;-coumaric acid&amp;gt; &lt;em&gt;p&lt;/em&gt;-hydroxybenzoic acid). As a result, the fraction exhibited strong antioxidant activity evident by the ability of quenching DPPH and ABTS radicals, chelating capacity of Fe&lt;sup&gt;2+&lt;/sup&gt; as well as reducing components with EC&lt;sub&gt;50&lt;/sub&gt; of 1000 to 2264 &amp;mu;g/ml. Besides, the formulation also emerged as a potent source of antibiotic as it inhibited growth of investigating microbes in order of &lt;em&gt;Staphylococcus aureus&lt;/em&gt;&amp;gt; &lt;em&gt;Escherichia coli&lt;/em&gt;&amp;gt; &lt;em&gt;Bacillus subtilis&lt;/em&gt;&amp;gt; &lt;em&gt;Salmonella typhimurium&lt;/em&gt;&amp;gt; &lt;em&gt;Listeria monocytogenes&lt;/em&gt;. &lt;strong&gt;Conclusion:&lt;/strong&gt; Thus, the outcome might encourage use of &lt;em&gt;M. lobayensis&lt;/em&gt; as natural antioxidant and antibacterial agent in pharmaceutical, cosmetic or food industries.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1154</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Somanjana Khatua, Krishnendu Acharya* &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Botany, Molecular and Applied Mycology and Plant Pathology Laboratory, Centre of Advanced Study, University of Calcutta, 35, Ballygunge Circular Road, Kolkata - 700019, West Bengal, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Aryo Tedjo</style></author><author><style face="normal" font="default" size="100%">Fadilah Fadilah</style></author><author><style face="normal" font="default" size="100%">Ade Arsianti</style></author><author><style face="normal" font="default" size="100%">Rafika Indah Paramita</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Identification by Docking Simulation And In Vivo Effect of Essential Oil From Cinnamommum Burmannii as Antiobesity With Leptin Receptor In The Olfactory System of Mice Balb C</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July/2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">73-77</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aim:&lt;/strong&gt; This study examines the effect of inhalation of essential oil of cinnamon (&lt;em&gt;Cinnamomum burmannii&lt;/em&gt;) on the metabolic activity of hormone receptors olfactory system of mice balb C. &lt;strong&gt;Methodology:&lt;/strong&gt; Effects of agonist or antagonist compounds in cinnamon essential oil on metabolic hormone receptors in the olfactory system are predicted using molecular docking simulation. Changes in the metabolic processes that occur views of changes in body weight, change in food intake, as well as lipid profile and blood glucose of mice. &lt;strong&gt;Result:&lt;/strong&gt; The results showed Expression of leptin receptors (Lep-R) in the brains of mice given either inhalation of essential oils derived from the leaves and stems, in contrast to the control group who did not get essential oils. Provision of essential oils through inhalation increased lep-R expression in the brain of mice. Both in silico and in vivo evidence that essential oils from cinnamon plants are extracted from &lt;em&gt;Cinnamommum burmannii&lt;/em&gt; and given by inhalation in Balb C mice are known to improve glucose and lipid metabolism by reducing the concentration of serum leptin concentrations and increased sensitivity to insulin.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Keywords:&lt;/strong&gt; olfactory system, leptin receptors, &lt;em&gt;Cinnamomum burmannii&lt;/em&gt;, docking simulation, immunohistochemistry&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">73</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Kusmardi Kusmardi,1 Aryo Tedjo,&lt;sup&gt;2&lt;/sup&gt; Fadilah Fadilah,&lt;sup&gt;2&lt;/sup&gt; Ade Arsianti,&lt;sup&gt;2&lt;/sup&gt; Rafika Indah Paramita&lt;sup&gt;2&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt; 1&lt;/sup&gt;Department of Anatomical Pathology, Faculty of Medicine, University of Indonesia, Jakarta - 10430, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt; 2&lt;/sup&gt;Department of Medical Chemistry, Drug Development Research Center - IMERI, Faculty of Medicine, University of Indonesia, Jakarta - 10430, INDONESIA. *e-mail : fika.paramita@gmail.com / rafikaindah@ ui.ac.id&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Aryo Tedjo</style></author><author><style face="normal" font="default" size="100%">Fadilah Fadilah</style></author><author><style face="normal" font="default" size="100%">Ade Arsianti</style></author><author><style face="normal" font="default" size="100%">Rafika Indah Paramita</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Identification by Docking Simulation and in vivo Effect of Essential Oil from Cinnamommum burmannii as Anti-obesity with Leptin Receptor in the Olfactory System of Mice Balb C</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cinnamomum burmannii</style></keyword><keyword><style  face="normal" font="default" size="100%">docking simulation</style></keyword><keyword><style  face="normal" font="default" size="100%">immunohistochemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">leptin receptors</style></keyword><keyword><style  face="normal" font="default" size="100%">olfactory system</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">875-879</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aim:&lt;/strong&gt; This study examines the effect of inhalation of essential oil of cinnamon (&lt;em&gt;Cinnamomum burmannii&lt;/em&gt;) on the metabolic activity of hormone receptors olfactory system of mice Balb C. &lt;strong&gt;Methodology:&lt;/strong&gt; Effects of agonist or antagonist compounds in cinnamon essential oil on metabolic hormone receptors in the olfactory system are predicted using molecular docking simulation. Changes in the metabolic processes that occur views of changes in body weight, change in food intake, as well as lipid profile and blood glucose of mice. &lt;strong&gt;Result:&lt;/strong&gt; The results showed Expression of leptin receptors (Lep-R) in the brains of mice given either inhalation of essential oils derived from the leaves and stems, in contrast to the control group who did not get essential oils. Provision of essential oils through inhalation increased lep-R expression in the brain of mice. Both &lt;em&gt;in silico&lt;/em&gt; and &lt;em&gt;in vivo&lt;/em&gt; evidence that essential oils from cinnamon plants are extracted from &lt;em&gt;Cinnamommum burmannii&lt;/em&gt; and given by inhalation in Balb C mice are known to improve glucose and lipid metabolism by reducing the concentration of serum leptin concentrations and increased sensitivity to insulin.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">875</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Kusmardi Kusmardi&lt;sup&gt;1&lt;/sup&gt;, Aryo Tedjo&lt;sup&gt;2&lt;/sup&gt;, Fadilah Fadilah&lt;sup&gt;2&lt;/sup&gt;, Ade Arsianti&lt;sup&gt;2&lt;/sup&gt;, Rafika Indah Paramita&lt;sup&gt;2*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anatomical Pathology, Faculty of Medicine, University of Indonesia, Jakarta - 10430, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medical Chemistry, Drug Development Research Center - IMERI, Faculty of Medicine, University of Indonesia, Jakarta - 10430, INDONESIA.&amp;nbsp;&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kunal</style></author><author><style face="normal" font="default" size="100%">Subbalakshmi Narasajjana Krishnadasa</style></author><author><style face="normal" font="default" size="100%">Pai Sheila R</style></author><author><style face="normal" font="default" size="100%">Rashmi Kaup Shiva</style></author><author><style face="normal" font="default" size="100%">Nayanatara Arunkumar</style></author><author><style face="normal" font="default" size="100%">Vinodini Nithyananda Anantharaya</style></author><author><style face="normal" font="default" size="100%">Pratik Kumar Chatterjee</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Impact of Regularly Supervised Training of Pranayama and Omkar Meditation on the Cardio-Respiratory Parameters and Short-Term Memory of Persons with Special Needs</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Meditation</style></keyword><keyword><style  face="normal" font="default" size="100%">Mental retardation</style></keyword><keyword><style  face="normal" font="default" size="100%">Pranayama</style></keyword><keyword><style  face="normal" font="default" size="100%">Short term memory</style></keyword><keyword><style  face="normal" font="default" size="100%">Yoga</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/491</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">366-370</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Yogic practices are known to affect the cardiac, respiratory and mental status of people. &lt;strong&gt;Objective:&lt;/strong&gt; To investigate if the regularly supervised training of pranayama and meditation affects the basic cardio-respiratory parameters and short-term-memory (STM) of mentally challenged young adults. &lt;strong&gt;Material and methods:&lt;/strong&gt; 80 mentally challenged young adults attending a special school were randomly divided into the control group and Yoga group. Yoga group performed &lt;em&gt;Naadishodhan, Kapalbhati pranayama&lt;/em&gt; and &lt;em&gt;Aum Chanting&lt;/em&gt; under total supervision for 30 min daily for 3 weeks, except on Sundays. Control group was involved with the regular school curriculum. The parameters were measured twice, before (baseline) and after (follow-up) the study period. STM was evaluated under two subcategories, first by the ability to repeat the numbers in reverse order and second, repeating the words in the same order. Respiratory rate, pulse, systolic and diastolic blood pressures were measured as cardio-respiratory parameters. &lt;strong&gt;Results:&lt;/strong&gt; Both groups had similar baseline scores. At follow-up, highly significant improvements were observed in Yoga-group as compared to control. In the Yoga-group scores of both the sub-categories of STM were higher, respiratory-rate and heart-rate were lower but was within normal range. However, both systolic and diastolic blood pressures of Yoga group showed no changes as compared to control. &lt;strong&gt;Conclusion:&lt;/strong&gt; The pranayama and meditation has beneficial influences on heart rate, breathing rate and STM of mentally-challenged people.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">366</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Kunal*, Subbalakshmi Narasajjana Krishnadasa, Pai Sheila R., Rashmi Kaup Shiva, Nayanatara Arunkumar, Vinodini Nithyananda Anantharaya, Pratik Kumar Chatterjee &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Physiology, Kasturba Medical College (KMC), Manipal Academy of Higher Education (MAHE),&amp;nbsp;Mangalore, Karnataka, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Palanisamy Sampathkumar</style></author><author><style face="normal" font="default" size="100%">Subramanian Kalavathy</style></author><author><style face="normal" font="default" size="100%">Arumugam Vijaya Anand</style></author><author><style face="normal" font="default" size="100%">Thangavelu Sangeetha</style></author><author><style face="normal" font="default" size="100%">Purusothaman Sujeetha</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Impact of Tridax procumbens on Hematological Parameters in aflatoxin Induced Liver Toxicity in Albino Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacog Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">alfatoxin</style></keyword><keyword><style  face="normal" font="default" size="100%">etc</style></keyword><keyword><style  face="normal" font="default" size="100%">Haemoglobin</style></keyword><keyword><style  face="normal" font="default" size="100%">Packed cell volume</style></keyword><keyword><style  face="normal" font="default" size="100%">Prothrombin time</style></keyword><keyword><style  face="normal" font="default" size="100%">Red blood corpus cells</style></keyword><keyword><style  face="normal" font="default" size="100%">Tridax procumbens</style></keyword><keyword><style  face="normal" font="default" size="100%">White blood corpus cells</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January-2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/483</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">304-308</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; &lt;em&gt;Tridax procumbens &lt;/em&gt;comes under the family Asteraceae Tridax which is found to have anti-inflammatory, analgesic properties. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The morphological parameters such as the body weight, liver and kidney weight of experimental animals which were fed by alfatoxin and thereby treating with extracts of &lt;em&gt;T. procumbens&lt;/em&gt; were studied along with the Hematological parameters such as Haemoglobin (Hb), Red Blood Corpus Cells (RBC), White Blood Corpus Cells (WBC) , Packed Cell Volume (PCV) and Prothrombin time (PT). &lt;strong&gt;Results:&lt;/strong&gt; The results of this study shows that there is an significant changes in the body weight liver and kidney weight in &lt;em&gt;T. procumbens&lt;/em&gt; treated animals and also significant raise in blood level was seen in the &lt;em&gt;T. procumbens &lt;/em&gt;treated animals. &lt;strong&gt;Conclusion:&lt;/strong&gt; Based on the results obtained, we concluded that &lt;em&gt;T. procumbens&lt;/em&gt; have an antiaflatoxicosis potency.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">304</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Palanisamy Sampathkumar&lt;sup&gt;1,&lt;/sup&gt; Subramanian Kalavathy&lt;sup&gt;2&lt;/sup&gt;, Arumugam Vijaya Anand&lt;sup&gt;3&lt;/sup&gt;, Thangavelu Sangeetha&lt;sup&gt;3&lt;/sup&gt;, Purusothaman Sujeetha&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;3&lt;/strong&gt; &lt;/sup&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry and Biosciences, SASTRA Deemed University, Srinivasa Ramanujan Centre, Kumbakonam, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Botany, Bishop Heber College,Thiruchirappalli,Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Human Genetics and Molecular Biology, Bharathiar University, Coimbatore,Tamil Nadu, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kusmardi Kusmardi</style></author><author><style face="normal" font="default" size="100%">Tedjo Aryo</style></author><author><style face="normal" font="default" size="100%">Wuyung Puspita Eka</style></author><author><style face="normal" font="default" size="100%">Fadilah Fadilah</style></author><author><style face="normal" font="default" size="100%">Priosoeryanto Bambang Pontjo</style></author><author><style face="normal" font="default" size="100%">Fachri Wilzar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In silico, in vitro and in vivo Tests of Ficus deltoidea Jack Leaves Extract as Inhibitor for Beta-Catenin Expression in Colon Carcinogenesis Model</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Azoxymethane</style></keyword><keyword><style  face="normal" font="default" size="100%">Colon carcinogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Ficus deltoidea</style></keyword><keyword><style  face="normal" font="default" size="100%">in silico</style></keyword><keyword><style  face="normal" font="default" size="100%">β-catenin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/675</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">808-813</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Context:&lt;/strong&gt; &lt;em&gt;Ficus deltoidea&lt;/em&gt; Jack leaves extract as anticolorectal cancer. &lt;strong&gt;Aims:&lt;/strong&gt; This study aims to analyze the potential of FD extract to be an anti-colon cancer by investigating the extract capability in reducing &amp;beta;-catenin expression and inhibiting colon cancer cells growth. &lt;strong&gt;Settings |and Design:&lt;/strong&gt; The research was conducted in Medical Faculty Universitas Indonesia with experimental design. &lt;strong&gt;Methods and Material:&lt;/strong&gt; FD ethanol extracts was tested in vitro, in silico and &lt;em&gt;in vivo&lt;/em&gt;. &lt;em&gt;In vitro&lt;/em&gt; test was conducted to human colon cell lines. &lt;em&gt;In vivo&lt;/em&gt; test was conducted to Balb/c mice induced with 10 mg/kg azoxymethane (AOM) and dextran sodium sulfate 1% (DSS). The colonic tissue collected was the distal portion. &amp;beta;-catenin expressions in the cytoplasm and nuclei of the epithelial cells of the colon crypt were semi quantitatively assessed using the immunohistochemistry staining on ten visual fields with 400x magnification. &lt;strong&gt;Statistical analysis used:&lt;/strong&gt; SPSS. &lt;strong&gt;Results:&lt;/strong&gt; FD ethanol extracts inhibit the expression of &amp;beta;-catenin in the crypt ephitelial cells of mice colon induced with AOM/DSS. The extracts also inhibit the growth of human colon cancer (HCT 116) with IC&lt;sub&gt;50&lt;/sub&gt; value of 5.41 mg/mL. Phytochemical screening to the extracts gave three groups of compounds: alkaloid, flavonoid, and tannin. Water fraction is the best fraction. Based on in the results of in silico analysis with molecular docking, FD extract is believed to influence the expression of &amp;beta;-catenin, in which vitexin and isovitexin are the main candidate compounds to influence the expression of the protein. &lt;strong&gt;Conclusion:&lt;/strong&gt; FD ethanol extract is potential to be an anti-colon cancer proven by the extract capability to reduce &amp;beta;-catenin expression.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">808</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Kusmardi Kusmardi&lt;sup&gt;1&lt;/sup&gt;, Tedjo Aryo&lt;sup&gt;2&lt;/sup&gt;, Wuyung Puspita Eka&lt;sup&gt;1&lt;/sup&gt;, Fadilah&lt;sup&gt;2&lt;/sup&gt;, Priosoeryanto Bambang Pontjo&lt;sup&gt;3&lt;/sup&gt;, Fachri Wilzar&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;4&lt;/strong&gt;* &lt;/sup&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anatomic Pathology, Faculty of Medicine, Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Deparment of Chemisty, Faculty of Medicine Universitas Indonesia, Jakarta, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Laboratory of Pathology, Faculty of Veterinary, Institut Pertanian Bogor, Bogor, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Drug Development Research Center, Indonesian Medical Education and Research Institute, Faculty of Medicine Universitas Indonesia, INDONESIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Micheylla Kusumaning Dewi</style></author><author><style face="normal" font="default" size="100%">Ade Arsianti</style></author><author><style face="normal" font="default" size="100%">Cut Raisya Zahira Zagloel</style></author><author><style face="normal" font="default" size="100%">Yully Astika Nugrahayning Aziza</style></author><author><style face="normal" font="default" size="100%">Kartika Dwi Kurniasari</style></author><author><style face="normal" font="default" size="100%">Baiq Kirana Dyahningrum Mandasari</style></author><author><style face="normal" font="default" size="100%">Riathul Masita</style></author><author><style face="normal" font="default" size="100%">Futihati Ruhama Zulfa</style></author><author><style face="normal" font="default" size="100%">Norma Nur Azizah</style></author><author><style face="normal" font="default" size="100%">Rista Putrianingsih</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In vitro Evaluation of Seaweed Gracilaria verrucosa for Cytotoxic Activity against Cervical HeLa Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Gracillaria verrucosa</style></keyword><keyword><style  face="normal" font="default" size="100%">HeLa cervical cancer cells</style></keyword><keyword><style  face="normal" font="default" size="100%">IC50 value</style></keyword><keyword><style  face="normal" font="default" size="100%">MTT Assay</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">1007-1011</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Seaweed macroalgae of &lt;em&gt;Gracilaria verrucosa &lt;/em&gt;has been known to have a potent anticancer activity, however the cytotoxicity against cervical cancer has not been explored further. &lt;strong&gt;Objective:&lt;/strong&gt; This study aims to utilize Indonesia&amp;rsquo;s marine resource which is focused on seaweed macroalgae G. verrucosa as a future anti-cervical cancer agent. &lt;strong&gt;Materials and Method:&lt;/strong&gt; Seaweed &lt;em&gt;G. verrucosa&lt;/em&gt; originated from Labuan Aji beach, Nusa Tenggara Barat, Indonesia, extracted, macerated, and fractionated into four organic solvents of different polarity, consisting of hexane, ethyl acetate, chloroform and ethanol. Then, the macroalgae extracts are diluted into 8 different concentrations. Afterwards,&lt;em&gt; in vitro&lt;/em&gt; anticancer activity evaluation of hexane, ethyl acetate, chloroform and ethanol extracts of &lt;em&gt;G. verrucosa&lt;/em&gt; against cervical HeLa cells were conducted by MTT cell proliferation assay. Triplo mechanism is also applied in this study to increase the accuracy of the results. The anticancer activity is measured using IC&lt;sub&gt;50&lt;/sub&gt; value. &lt;strong&gt;Results:&lt;/strong&gt; The four concentrated extracts &lt;em&gt;G. verrucosa &lt;/em&gt;showed cytotoxicity against cervical HeLa cells. The greatest anticancer activity is depicted by hexane extract with an IC&lt;sub&gt;50&lt;/sub&gt; of 14.94 &amp;mu;g/mL, followed by chloroform (IC&lt;sub&gt;50&lt;/sub&gt; 15.74 &amp;mu;g/mL), ethyl acetate (IC&lt;sub&gt;50&lt;/sub&gt; 16.18 &amp;mu;g/mL), and ethanol (IC&lt;sub&gt;50&lt;/sub&gt; 19.43 &amp;mu;g/mL). &lt;strong&gt;Conclusion:&lt;/strong&gt; Our results clearly indicate that hexane, ethanol, chloroform, and ethyl acetate extracts of seaweed &lt;em&gt;G. verrucosa&lt;/em&gt; can be further developed to be anti-cervical cancer agents, with hexane extract displaying the greatest cytotoxic effect.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1007</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Micheylla Kusumaning Dewi&lt;sup&gt;1&lt;/sup&gt;, Ade Arsianti&lt;sup&gt;2,3*&lt;/sup&gt;, Cut Raisya Zahira Zagloel&lt;sup&gt;1&lt;/sup&gt;, Yully Astika Nugrahayning Aziza&lt;sup&gt;1&lt;/sup&gt;, Kartika Dwi Kurniasari&lt;sup&gt;1&lt;/sup&gt;, Baiq Kirana Dyahningrum Mandasari&lt;sup&gt;1&lt;/sup&gt;, Riathul Masita&lt;sup&gt;1&lt;/sup&gt;, Futihati Ruhama Zulfa&lt;sup&gt;1&lt;/sup&gt;, Norma Nur Azizah&lt;sup&gt;3&lt;/sup&gt;, Rista Putrianingsih&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Medical Student, Department of Medical Chemistry, Faculty of Medicine University of Indonesia, Depok, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Medical Chemistry, Faculty of Medicine, University of Indonesia, Depok, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Drug Development Research Cluster, Drug Discovery Division, Indonesia Medical Education and Research Institute (IMERI), Faculty of Medicine, University of Indonesia, Jalan Salemba Raya 6 Jakarta 10430, INDONESIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wanwisa Khunawattanakul</style></author><author><style face="normal" font="default" size="100%">Passakorn Boonma</style></author><author><style face="normal" font="default" size="100%">Ronnarit Kampetch</style></author><author><style face="normal" font="default" size="100%">Achida Jaruchotikamol</style></author><author><style face="normal" font="default" size="100%">Benjamart Cushnie</style></author><author><style face="normal" font="default" size="100%">Sakulrat Rattanakiat</style></author><author><style face="normal" font="default" size="100%">Pawitra Pulbutr</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Inhibitory Actions of Lagerstroemia speciosa (L.) Pers. Aqueous and Ethanolic Leaf Extracts against Carbohydrate-digesting Enzymes</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Diabetes mellitus</style></keyword><keyword><style  face="normal" font="default" size="100%">Lagerstroemia speciosa (L.) Pers.</style></keyword><keyword><style  face="normal" font="default" size="100%">α-amylase</style></keyword><keyword><style  face="normal" font="default" size="100%">α-glucosidase</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">s113-s118</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Context:&lt;/strong&gt; The leaves of &lt;em&gt;Lagerstroemia speciosa&lt;/em&gt; (L.) Pers. (banaba) have been consumed traditionally in several Southeast Asian countries for the treatment of diabetes mellitus. The plasma glucose lowering actions of this medicinal plant were proposed to be linked with several mechanisms of action. However, its inhibitory actions against &amp;alpha;-amylase and &amp;alpha;-glucosidase, which play a major role in the regulation of postprandial plasma glucose, have not been clearly established. &lt;strong&gt;Aims:&lt;/strong&gt; This study thus aimed to investigate the effects of &lt;em&gt;Lagerstroemia speciosa&lt;/em&gt; (L.) Pers. aqueous and ethanolic leaf extracts (LSA and LSE extracts, respectively) on in vitro carbohydrate-digesting enzyme activities and enzyme kinetics. Settings and Design: In vitro carbohydrate-digesting enzyme activity assay. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The activities of &amp;alpha;-amylase and &amp;alpha;-glucosidase were indicated by the amounts of maltose and p-nitrophenol generated in the reactions, respectively.&lt;strong&gt; Statistical analysis used:&lt;/strong&gt; The data were analysed by using one-way ANOVA, followed by Bonferroni post-hoc test. &lt;strong&gt;Results:&lt;/strong&gt; The LSA extract significantly inhibited both &amp;alpha;-amylase and &amp;alpha;-glucosidase enzymes with the IC&lt;sub&gt;50&lt;/sub&gt;s of 1.21&amp;plusmn;0.16 and 49.71&amp;plusmn;0.86 &amp;mu;g/mL, respectively. Meanwhile, the LSE extract selectively inhibited &amp;alpha;-amylase activity (IC&lt;sub&gt;50 &lt;/sub&gt;= 22.21&amp;plusmn;4.00 &amp;mu;g/mL) with no apparent inhibition against &amp;alpha;-glucosidase activity. Both LSA and LSE extracts inhibited &amp;alpha;-amylase enzyme in a mixed inhibition manner whilst the LSA extract also acted as a mixed inhibitor against &amp;alpha;-glucosidase enzyme. The extracts possessed higher binding affinities toward the enzymes, indicated by the lower Ki values, when compared to acarbose (positive control). &lt;strong&gt;Conclusion:&lt;/strong&gt; These results suggest the potential use of the extracts for a control of postprandial plasma glucose.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s113</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Wanwisa Khunnawattanakul, Passakorn Boonma, Ronnarit Kampetch, Achida Jaruchotikamol, Benjamart Cushnie, Sakulrat Rattanakiat, Pawitra Pulbutr&lt;sup&gt;*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Pharmaceutical Chemistry and Natural Product Research Unit, Faculty of Pharmacy, Mahasarakham University, Maha Sarakham, 44150, THAILAND.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vasuki K</style></author><author><style face="normal" font="default" size="100%">Murugananthan G</style></author><author><style face="normal" font="default" size="100%">Banupriya C</style></author><author><style face="normal" font="default" size="100%">Ramya R</style></author><author><style face="normal" font="default" size="100%">Mohana priya C</style></author><author><style face="normal" font="default" size="100%">Shenjudar D</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Investigation of Immunomodulatory Potential of Whole Plant of Boerhavia erecta Linn.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Boerhavia erecta</style></keyword><keyword><style  face="normal" font="default" size="100%">Candida albicans</style></keyword><keyword><style  face="normal" font="default" size="100%">Phagocytosis stimulation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">January 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/472</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">241-244</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;The present study was designed to investigate immunomodulatory activity of aqueous extract of whole plant &lt;em&gt;Boerhavia erecta&lt;/em&gt;. The concept of immunomodulation has been gaining much significance worldwide as people started realizing the indispensible role of the immune system in maintaining a disease-free state. Natural products have been considered a plentiful source in the search for new chemical entities that modulate the immune system with reduced adverse effects. Pharmacological evaluation of the crude ethanolic extract of &lt;em&gt;Boerhavia diffusa &lt;/em&gt;roots has shown to possess anti proliferative and immunomodulatory properties but not reported from &lt;em&gt;Boerhavia erecta&lt;/em&gt;. Due to that, immunomodulatory activity was carried out for the aqueous extract of &lt;em&gt;Boerhavia erecta&lt;/em&gt; (Family: Nyctaginaceae). In this present study, aqueous extract of whole plant of &lt;em&gt;Boerhavia erecta&lt;/em&gt; exhibited phagocytosis stimulation of human neutrophils against &lt;em&gt;Candida albicans&lt;/em&gt; in a dose dependent manner.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">241</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Vasuki K&lt;sup&gt;1&lt;/sup&gt;*, Murugananthan G&lt;sup&gt;1&lt;/sup&gt;, Banupriya C&lt;sup&gt;2&lt;/sup&gt;, Ramya R&lt;sup&gt;2&lt;/sup&gt;, Mohana Priya C&lt;sup&gt;2&lt;/sup&gt;, Shenjudar D&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Swamy Vivekanandha College of Pharmacy, Tiruchengode, Tamil Nadu, INDIA - 637 205.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;U.G. Students, Swamy Vivekanandha College of Pharmacy, Tiruchengode, Tamil Nadu, INDIA - 637 205.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lubna Abu-Niaaj</style></author><author><style face="normal" font="default" size="100%">Ibrahim Katampe</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Isolation and Characterization of Flavones from Artemisia monosperma</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimicrobial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidants</style></keyword><keyword><style  face="normal" font="default" size="100%">Artemisia monosperma</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavones</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">1018-1023</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Artemisia monosperma&lt;/em&gt; (Delile) is a green aromatic shrub that grows widely in the deserts of Middle East, Africa and China. This plant is commonly used in folk medicine as a remedy of a wide range of illness including gastrointestinal disorders, inflammation, diabetes and microbial infection. The different categories of the secondary metabolites identified from Artemisia species are recognized for their biological activities as antioxidants, anti-inflammatory and antimicrobial compounds. &lt;strong&gt;Objective:&lt;/strong&gt; This study aims to isolate new flavonoids from &lt;em&gt;A. monosperma&lt;/em&gt; that might have potential biological activities thus be translated into pharmaceutical uses. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Air-dried &lt;em&gt;A. monosperma&lt;/em&gt; extraction was done using different organic solvents. The methanolic extract was selected for isolation of flavonoids using column chromatography and thin layer chromatography. The chemical structures of the isolated flavones determined based on spectroscopic analysis of ultraviolet, mass and nuclear magnetic resonance spectra.&lt;strong&gt; Results:&lt;/strong&gt; Nine flavone aglycones were isolated and identified from the methanolic extract; four of which are reported for the first time from &lt;em&gt;A. monosperma&lt;/em&gt;. These include: 5-Hydroxy-3',4', 6,7-tetramethoxyflavone; 3',5-dihydroxy-4',6,7-trimethoxyflavone (eupatorin); 5,6-dihydroxy-4',7-dimethoxyflavone(ladanein); and 2',4',5-trihydroxy-5',6,7&amp;ndash; trimethoxyflavone (arcapillin). The remaining five flavones were previously identified from this plant as : 4',5-Dihydroxy-3',6,7-tri-methoxyflavone(cirsilineol);5,7-dihydroxy-3',4',6-trimethoxyflavone (eupatilin);4',5,7-trihydroxy-3',6-dimethoxyflavone(jaceosidin);4',5-dihydroxy-6,7-dimethoxy- flavone (circimaritin) and 4',5,7-trihydroxy-6-methoxyflavone (hispidulin). In addition, two acetophenone derivatives were isolated from fractions yielded selected flavones and these were identified as 4-hydroxyacetophenone and 3-(2-hydroxymethyl-2-buten-4-yl)-4-hydroxyaceto- phenone. &lt;strong&gt;Conclusion:&lt;/strong&gt; This successful isolation of these natural flavonoids from &lt;em&gt;A. monosperma&lt;/em&gt; can contribute further to the evaluation of bioactive compounds against disorders including but not limited to inflammatory associated disorders and microbial infections.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1018</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Lubna Abu-Niaaj* Ibrahim Katampe&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Natural Sciences, Central State University, 1400 Brush Row Road, Wilberforce, OH 45384, USA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">M Janib Achmad</style></author><author><style face="normal" font="default" size="100%">Alim Isnansetyo</style></author><author><style face="normal" font="default" size="100%">Noer Kasanah</style></author><author><style face="normal" font="default" size="100%">Ustadi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Macrophage Immunomodulatory Activity of Unsaturated Fatty Acid Isolated from the Crown-of-thorns Star Fish (acanthaster planci)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acanthaster planci</style></keyword><keyword><style  face="normal" font="default" size="100%">Immunomodulatory</style></keyword><keyword><style  face="normal" font="default" size="100%">North moluccas</style></keyword><keyword><style  face="normal" font="default" size="100%">Phagocytic capacity</style></keyword><keyword><style  face="normal" font="default" size="100%">Phagocytic index</style></keyword><keyword><style  face="normal" font="default" size="100%">Ternate island</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">951-957</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Immunomodulator are chemical compounds that can improve the body&amp;rsquo;s defense mechanisms both specific and non-specific, and non-specific induction of both cellular and humoral defense mechanisms.&lt;strong&gt; Objectives:&lt;/strong&gt; The objectives of this study were to investigate immunomodulator activity and to identify the chemical constituents of active fractions from star fish&lt;em&gt; Acanthaster planci&lt;/em&gt;, based on bioassay guided isolation.&lt;strong&gt; Materials and Methods:&lt;/strong&gt; &lt;em&gt;A. planci&lt;/em&gt; was collected from Ternate Island, North Moluccas, extracted with distilled methanol, partitioned with gradient chloroform-hexane-water and fractionated in column chromatography using silica gel and gradient hexane-ethyl acetate. Profiling chemical constituent was done by thin layer chromatograpahy and GC-MS. The immunomodulator activity was measured based on percentage of phagocytic capacity (PC) and phagocytic index (PI). &lt;strong&gt;Results:&lt;/strong&gt; The result showed that 3 partition fractions exhibited immunomodulator activity. Data analysis exhibited that the best fraction was hexane fraction, and the best dosesmost effective doses of PC and PI were at 0.5 mg/kg body weight (BW) and 0.7 mg/kg BW, respectively. Data analysis of the 3 hexane fractions exhibited that the best fraction was fraction 3 and the best doses of PC was at 0.5 mg/kg BW and that of PI was at 0.7 mg/kg BW. Metabolites analysis using GC-MS yielded a number of chemical constituents of fraction 2 dan fraction 3 that dominated by unsaturated fatty acid. The study concluded that star fish &lt;em&gt;A. planci&lt;/em&gt; from Ternate Island has a potential source of immunomodulator.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">951</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;M Janib Achmad&lt;sup&gt;1&lt;/sup&gt;, Alim Isnansetyo&lt;sup&gt;2&lt;/sup&gt;, Noer Hasanah&lt;sup&gt;2&lt;/sup&gt;,Ustadi&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Fisheries and Marine Science, University of Khairun Ternate Jl.Pertamina Kampus 2, Kel. Gambesi Ternate Selatan, INDONESIA. &lt;sup&gt;2&lt;/sup&gt;Department of Fisheries, University of Gadjah Mada Jl Flora Buluksumur, Yogyakarta, INDONESIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sri Kumalaningsih</style></author><author><style face="normal" font="default" size="100%">Muhammad Arwani</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nutritious Pure Herbal Whitening Sun Cream Processed from Seed and Leaf of Moringa oleifera Fortified with Red Rice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Herbal</style></keyword><keyword><style  face="normal" font="default" size="100%">Moringa oleifera</style></keyword><keyword><style  face="normal" font="default" size="100%">Red Rice</style></keyword><keyword><style  face="normal" font="default" size="100%">Sun Cream</style></keyword><keyword><style  face="normal" font="default" size="100%">ZnO</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/401</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">77-80</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;em&gt;Moringa oleifera&lt;/em&gt; seed and leaf contained available medium fatty acid profile and essential amino acid bound in the tissue which should be hydrolysed. The addition of red rice which has antioxidant compound namely ZnO that can have protected the skin from sun burn and also to make the gelatinous slurry due to reducing the moisture content. The utilization of oil seed and leaf as raw material and fortified with red rice for making a low-cost sun cream is beneficial mainly for women living at rural region. Two phases of experiments were carried out. The first phase was the effect of time and temperature on the yield and oleic acid content of the oil. A randomized block design with two factors was carried out. The temperature at three level (50, 55, 60oC) as the first factor, and the time of extraction at three levels (12, 15, 20 hours) as the second factor. It was found that treatment of 50oC at 20 hours extraction shown the best result. The yield of oil was 34% and the oleic acid content was a 71.9% from the extracted oil. A randomized block design was used to carried out the second phase of study. The time of steaming (30, 45, 60 minutes) as the first factor and the red rice concentration (5%, 10%, 15%) as the second factor. The result shown that the use of 60 minutes and 5% red rice concentration was the best result. The slurry has the moisture content of 40.4% and the protein content was 40.5%. The storage stability of the sun cream stored under low temperature (30&amp;plusmn;1oC) was 6 months and the characteristic of the slurry having oleic acid, essential amino acid and the ZnO.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">77</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Sri Kumalaningsih&lt;sup&gt;1&lt;/sup&gt;, Muhammad Arwani&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Agro-industrial Technology Brawijaya University, St Veteran 65145 Malang, East Java, INDONESIA.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Graduate Student of Agricultural Technology, Brawijaya University St Veteran 65145 Malang, East Java, INDONESIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pallavi Malleshappa</style></author><author><style face="normal" font="default" size="100%">Ramesh Chapeyil Kumaran</style></author><author><style face="normal" font="default" size="100%">Krishna Venkatarangaiah</style></author><author><style face="normal" font="default" size="100%">Sameera Parveen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Peels of Citrus Fruits: A Potential Source of Anti-inflammatory and Anti-nociceptive Agents</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Carrageenan</style></keyword><keyword><style  face="normal" font="default" size="100%">Citrus peel</style></keyword><keyword><style  face="normal" font="default" size="100%">Hot plate</style></keyword><keyword><style  face="normal" font="default" size="100%">HRBC</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword><keyword><style  face="normal" font="default" size="100%">Tail immersion</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">s172-s178</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The present study was contemplated to evaluate the anti-inflammatory and analgesic potentials in peels of some commercially grown Citrus fruits of South India &lt;em&gt;viz&lt;/em&gt;, Lime (&lt;em&gt;Citrus aurantifolia)&lt;/em&gt;, Orange (&lt;em&gt;Citrus reticulata&lt;/em&gt;), Sour Orange (&lt;em&gt;Citrus aurantium&lt;/em&gt;), Pomello (&lt;em&gt;Citrus grandis&lt;/em&gt;) and Citron (Citrus medica).&lt;strong&gt; Methods:&lt;/strong&gt; The peel of the fruits were separated and subjected to cold extraction using 70% alcohol. The extracts obtained were screened for the presence of phytoconstituents by qualitative phytochemical analysis; the anti-inflammatory activity of extracts at 250 and 500mg/Kg body weight concentrations were assessed by &lt;em&gt;in vivo&lt;/em&gt; Carrageenan induced rat paw edema model and &lt;em&gt;in vitro&lt;/em&gt; HRBC membrane stabilization assay whereas Tail immersion and Hot plate methods have been used to evaluate their analgesic property. Results: The results revealed that, all extracts treated animals have shown significant decrease in paw edema volume at 3&lt;sup&gt;rd&lt;/sup&gt; and 4&lt;sup&gt;th &lt;/sup&gt;hour of treatment and increase in reaction time in tail immersion and hot plate readings at 120 and 150 min and are comparable to the standards. From the results it was evident that Citron peel extract exhibited significant antiinflammatory and analgesic property in all models. Preliminary phytochemical investigation revealed that extracts were bestowed with presence of flavonoids, terpenoids, steroids, glycosides, alkaloids, carotenoids and phenolic compounds which might be responsible for the antinociceptive and anti-inflammatory activities. &lt;strong&gt;Conclusion:&lt;/strong&gt; From the results it was evident that all citrus fruits have prominent activity in terms of parameters assessed in a dose dependent manner and are more effective in the later phase. The study thus documents that Citrus peels are good sources of anti-inflammatory and anti-nociceptive agents.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s172</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Pallavi Malleshappa&lt;sup&gt;1&lt;/sup&gt;, Ramesh Chapeyil Kumaran&lt;sup&gt;1,*&lt;/sup&gt;, Krishna Venkatarangaiah&lt;sup&gt;2&lt;/sup&gt;, Sameera Parveen&lt;sup&gt;1 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of PG studies and Research in Biotechnology, Sahyadri Science College, Kuvempu University, Shimoga - 577 203, Karnataka, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt; 2&lt;/sup&gt;PG Department of Studies and Research in Biotechnology, Kuvempu University, Jnana Sahyadri, Shankaraghatta - 577 451, Shimoga, Karnataka, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Akanksha Srivastava</style></author><author><style face="normal" font="default" size="100%">Kuldeep Awasthi</style></author><author><style face="normal" font="default" size="100%">Bhanu Kumar</style></author><author><style face="normal" font="default" size="100%">Ankita Misra</style></author><author><style face="normal" font="default" size="100%">Sharad Srivastava</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic and Pharmacological Evaluation of Hyssopus officinalis L. (Lamiaceae) Collected from Kashmir Himalayas, India</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">HPTLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Hyssopus officinalis</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolic acids</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/652</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">690-693</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Hyssopus officinalis&lt;/em&gt; L. is a well-known herb for its culinary and medicinal significance. The purpose of this study was to perform the pharmacognostic evaluation. &lt;strong&gt;Methods:&lt;/strong&gt; Physicochemical and phytochemical analysis, HPTLC quantification and &lt;em&gt;in vitro&lt;/em&gt; antioxidant and antidiabetic activity were done. Results: Preliminary screening revealed the presence of phytomolecules such as alkaloid (0.99%), tannin (1.75%), sugar (1.96%) and starch (0.68%). Total phenolic and flavonoid content were found to be 2.32% and 1.16% respectively. HPTLC quantification data showed that the content of ferulic acid (0.034%) was higher than caffeic acid (0.0064%) on dry weight basis The IC&lt;sub&gt;50&lt;/sub&gt; value for the &lt;em&gt;in vitro&lt;/em&gt; DPPH radical scavenging assay was 0.50 &amp;mu;g/ml and &lt;em&gt;in vitro&lt;/em&gt; anti diabetic assay displayed IC50 value of 0.8366 mg/ml. &lt;strong&gt;Conclusion:&lt;/strong&gt; The study suggests presence of considerable amount of phenolic acids and antioxidant activity in the plant which supports its use in the traditional systems of medicine.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">690</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Akanksha Srivastava, Kuldeep Awasthi, Bhanu Kumar, Ankita Misra, Sharad Srivastava&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;*&lt;/strong&gt; &lt;/sup&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Pharmacognosy and Ethnopharmacology Division CSIR-National Botanical Research Institute, Lucknow, Uttar Pradesh, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Supattra Klangprapun</style></author><author><style face="normal" font="default" size="100%">Benjaporn Buranrat</style></author><author><style face="normal" font="default" size="100%">Wanida Caichompoo</style></author><author><style face="normal" font="default" size="100%">Somsak Nualkaew</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostical and Physicochemical Studies of Enhalus acoroides (L.F.) Royle (Rhizome)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Enhalus acoroides</style></keyword><keyword><style  face="normal" font="default" size="100%">Macroscopic</style></keyword><keyword><style  face="normal" font="default" size="100%">Microscopic</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognostic</style></keyword><keyword><style  face="normal" font="default" size="100%">Specification</style></keyword><keyword><style  face="normal" font="default" size="100%">standardization</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">s89-s94</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The rhizome of&lt;em&gt; Enhalus acoroides&lt;/em&gt; (L.f.) Royle is used in traditional medicine for treatment of many diseases e.g. muscle pains, wounds and stomach problems where pharmacognostical studies are lacking. Many chemical constituents; luteolin, apigenin, luteolin glycosides, stigmasterol, daucosterol have been reported. The aim of this work was to perform a pharmacognostical evaluation. &lt;strong&gt;Methods:&lt;/strong&gt; Macroscopical, microscopical and physicochemical parameters were assessed.&lt;strong&gt; Results:&lt;/strong&gt; &lt;em&gt;E. acoroides&lt;/em&gt; has characteristic morphology. Microscopical studies indicated the presence of vessels, fiber, parenchyma cells, sclereids, tracheids and trichomes. Physicochemical parameters of &lt;em&gt;E. acoroides&lt;/em&gt; rhizome; foreign matter, loss on drying and total ash content were measured. As well as chemical investigation through TLC and HPLC were specified. &lt;strong&gt;Conclusion:&lt;/strong&gt; The present study of &lt;em&gt;E. acoroides&lt;/em&gt; rhizome provides useful information that can serve as a diagnostic tool for the standardization of &lt;em&gt;E. acoroides &lt;/em&gt;and will be helpful in characterization of the crude drug in the market.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s89</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Supattra Klangprapun&lt;sup&gt;1&lt;/sup&gt;, Benjaporn Buranrat&lt;sup&gt;1&lt;/sup&gt;, Wanida Caichompoo&lt;sup&gt;2&lt;/sup&gt;, Somsak Nualkaew&lt;sup&gt;2,* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Medicine, Mahasarakham University, Mahasarakham, THAILAND.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmaceutical Chemistry and Natural Product Research Unit, Faculty of Pharmacy, Mahasarakham University, Mahasarakham, THAILAND.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Achintya Kumar Mandal</style></author><author><style face="normal" font="default" size="100%">Shakila Ramachandran</style></author><author><style face="normal" font="default" size="100%">Kallingilkalathil Gopi Divya</style></author><author><style face="normal" font="default" size="100%">Mattumal Rubeena</style></author><author><style face="normal" font="default" size="100%">Koppala Narayana Sunil Kumar</style></author><author><style face="normal" font="default" size="100%">Parameswaran Sathiyarajeswaran</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostical-physico-chemical Evaluation and Development of HPTLC Finger print for Cichorium intybus L. fruits</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chicory fruits</style></keyword><keyword><style  face="normal" font="default" size="100%">Monograph</style></keyword><keyword><style  face="normal" font="default" size="100%">Quality control</style></keyword><keyword><style  face="normal" font="default" size="100%">standardization</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/653</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">694-699</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Many herbal medicines are lacking pharmacognostical, phytochemical, pharmacological and toxicological data even though used widely for medicinal purposes. &lt;em&gt;Cichorium intybus&lt;/em&gt; L. (Asteraceae) &amp;ndash; chicory is an ancient folklore medicine. Various parts of these plants are in use for a wide range of ailments including those affecting liver and kidney. The aim of the current study is to standardize the fruit of &lt;em&gt;C. intybus&lt;/em&gt; for macroscopy, microscopy, physicochemical parameters, TLC photo documentation along with development of HPTLC fingerprint profiles. &lt;strong&gt;Methods:&lt;/strong&gt; Following standard pharmacopoeial procedures, detailed macro-microscopic characterization along with preliminary phytochemical features of the drug has been recorded from the current study. &lt;strong&gt;Results:&lt;/strong&gt; Macro-microscopic study has revealed the authenticity of this medicinal achene type fruit. Physico-chemical and HPTLC studies revealed constants for identification and authentication of fruits of &lt;em&gt;C. intybus&lt;/em&gt;. Conclusion: The current study will serve as a reference tool for quality maintenance, authentication as well as scientific validation of chicory fruits.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">694</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Achintya Kumar Mandal, Shakila Ramachandran&lt;sup&gt;*&lt;/sup&gt;, Kallingilkalathil Gopi Divya, Mattumal Rubeena, Koppala Narayana Sunil Kumar, Parameswaran Sathiyarajeswaran &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Siddha Central Research Institute (Central Council for Research in Siddha, Ministry of AYUSH), Arignar Anna Hospital Campus, Arumbakkam, Chennai-600 106, Tamil Nadu, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Desmond Ato Koomson</style></author><author><style face="normal" font="default" size="100%">Benjamin Danso Kwakye</style></author><author><style face="normal" font="default" size="100%">Williams Kweku Darkwah</style></author><author><style face="normal" font="default" size="100%">Bismark Odum</style></author><author><style face="normal" font="default" size="100%">Mabel Asante</style></author><author><style face="normal" font="default" size="100%">Gideon Aidoo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Constituents, Total Saponins, Alkaloids, Flavonoids and Vitamin C Contents of Ethanol Extracts of five Solanum torvum Fruits</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alkaloids</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethanol Extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword><keyword><style  face="normal" font="default" size="100%">Saponins</style></keyword><keyword><style  face="normal" font="default" size="100%">Solanum torvum fruits</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">946-950</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Phytochemicals are frequently used in chemotherapeutic treatment or may be used as chemo preventive agents with chemoprevention. The study report the quantification of phytochemical constituents and vitamin C contents from ethanol extracts of Solanum torvum fruits. &lt;strong&gt;Method:&lt;/strong&gt; The main objective for this research was to use standard procedures to determine phytochemical and vitamin C content. &lt;strong&gt;Results:&lt;/strong&gt; The estimated alkaloids found in mature fruits were 6.32 &amp;plusmn; 0.12 mg/g and 16.94 &amp;plusmn; 2.3 mg/g in the immature fruits. Total saponins in mature and immature fruits were 8.60 &amp;plusmn; 2.6 mg/g and 16.90 &amp;plusmn; 9.4 mg/g respectively. Total flavonoids in mature and immature fruits were 21.14 &amp;plusmn; 4.4 mg/g and 14.24 &amp;plusmn; 1.8 mg/g respectively. Also vitamin C contents were 11.79 &amp;plusmn; 2.0 mg/g in mature fruits and 8.70 &amp;plusmn; 0.26 mg/g in immature fruits. With the exception of alkaloids whose difference in the mature and immature was significant, other differences obtained were not significant. &lt;strong&gt;Conclusion:&lt;/strong&gt; The study showed that the extracts contain diversity of phytochemicals in appreciable amount that can expertly keep the body against oxidative stress triggered by free radicals and therefore be used as a source of potent natural products.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">946</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Desmond Ato Koomson&lt;sup&gt;1&lt;/sup&gt;, Benjamin Danso Kwakye&lt;sup&gt;2&lt;/sup&gt;, Williams Kweku Darkwah&lt;sup&gt;1,3&lt;/sup&gt;*, Bismark Odum&lt;sup&gt;3,4&lt;/sup&gt;, Mabel Asante&lt;sup&gt;5&lt;/sup&gt;, Gideon Aidoo&lt;sup&gt;6&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biochemistry, School of Biological Sciences, University of Cape Coast, Cape Coast, GHANA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Mathematics, College of Science, Hohai University, Nanjing, CHINA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Key Laboratory of Integrated Regulation and Resource Development on Shallow Lakes, Ministry of Education, Environmental Engineering Department, College of Environment, Hohai University, Nanjing, CHINA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Chemical Engineering Department, College of Engineering, Kwame Nkrumah University of Science and Technology, Kumasi, GHANA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Laboratory Technology, School of Physical Sciences, University of Cape Coast, Cape Coast, GHANA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;Clinical Research Laboratory Department, 37-Military Teaching Hospital, Accra , GHANA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nilesh Balasaheb Chougule</style></author><author><style face="normal" font="default" size="100%">Sachin Annasaheb Nitve</style></author><author><style face="normal" font="default" size="100%">Kailasam Koumaravelou</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Investigation and Screening for Inflammatory Bowel Disease Activity of Ethanolic Extract of Kariyat</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Indomithacin.</style></keyword><keyword><style  face="normal" font="default" size="100%">Inflammatory bowel Disease</style></keyword><keyword><style  face="normal" font="default" size="100%">Kariyat</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">602-610</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objectives:&lt;/strong&gt; The present study investigates the protective effect of Kariyat against Indomethacin and Acetic Acid induced Inflammatory Bowel Disease in male wistar rats. &lt;strong&gt;Material Method:&lt;/strong&gt; HPTLC and GC-MS investigations indicated presence of steroid, phenols, terpenoid, alkaloids, saponine, flavonoids. IBD was induced by administration of Indomethacin (7.5mg/kg b.w. S.c.), Acetic Acid (4% v/v). Two different models used to induce IBD named Indomethacin induces enter colitis and Acetic Acid induces enter colitis in case of Indomethacin induces enter colitis the compromises 5 groups (n=6), normal, control, standard treated (Prednisolone 2mg/kg p.o.), KEE treated (100 mg/kg b.w.), KEE treated (200 mg/kg b.w.) in case of Acetic Acid induces colitis the compromises 5 groups (n=6), normal, control, standard treated (Prednisolone 2mg/kg p.o.), KEE treated (100mg/kg b.w.), KEE treated(200mg/kg b.w.). After treatment of 7 days animals were sacrificed and colon was isolated for macroscopic and microscopic studies. Quantification of inflammation was done by using myeloperoxidase assay (MPO), Lactate dehydrogenase (LDH), Lipid peroxidase (LPO). &lt;strong&gt;Result:&lt;/strong&gt; Evaluation based on macroscopic features showed significantly lower score values for drug treated and standard drug treated groups compared to the disease control groups. Histological examination of disease control group showed massive necrosis of the mucosa and sub mucosa. Drug treated group showed mild lesions, regeneration and inflammatory reaction. The Prednisolone treated group showed suppressed inflammatory reaction. The results observed from MPO, LDH and LPO assays showed significant improvement of disease with extract treated groups compared to disease control group. Histopathological examination of Kariyat treated group revealed less damage compared to Indomethacin and Acetic Acid Induced group. &lt;strong&gt;Conclusion:&lt;/strong&gt; Kariyat have shown to be effective in Indomethacin and Acetic Acid induced colitis in rats, which has protected the animals against experimentally induced disease because of its antioxidant and anti-inflammatory activity.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">602</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Nilesh Balasaheb Chougule&lt;sup&gt;1, 2&lt;/sup&gt;, Sachin Annasaheb Nitve&lt;sup&gt;1,3&lt;/sup&gt;, Kailasam Koumaravelou&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Centre for Research and Development, PRIST University, Vallam, Thanjavur 613 403, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Annasaheb Dange College of D. Pharmacy, Ashta, Sangli, Maharashtra, INDIA.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Anil Alias Pintu Magdum College of D. Pharmacy, Dharnggutti, Kolhapur, Maharashtra, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tamilarasan Tamil Kumar</style></author><author><style face="normal" font="default" size="100%">Seeni Mohamed Salique</style></author><author><style face="normal" font="default" size="100%">Mohamed Hussain Muhammad Ilyas</style></author><author><style face="normal" font="default" size="100%">Nooruddin Thajuddin</style></author><author><style face="normal" font="default" size="100%">Annamalai Panneerselvam</style></author><author><style face="normal" font="default" size="100%">Mohamed Khan Syed Ali Padusha</style></author><author><style face="normal" font="default" size="100%">Hussain Syed Jahangir</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Screening and Antimicrobial Studies in Leaf Extracts of Indigofera aspalathoides (Vahl.)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimicrobial activities</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Indigofera aspalathoides</style></keyword><keyword><style  face="normal" font="default" size="100%">MS</style></keyword><keyword><style  face="normal" font="default" size="100%">NMR</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">1208-1215</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; In traditional Indian herbal medicine, the plant &lt;em&gt;Indigofera aspalathoides&lt;/em&gt; (Vahl.) has been used to treat various human ailments. &lt;strong&gt;Methods and Results:&lt;/strong&gt; Various phytochemical compounds (Rf value) such as Tannin (1.14), Flavonoid (1.14), Saponin (0.87), Sterol (0.88) and Phenol (0.86) were found in the leaf extract. The antimicrobial effects of the phytoconstituents were examined for three bacterial and fungal species. The highest anti-bacterial and antifungal activities were found in flavonoid compound, where the maximum zone of inhibition was recorded in &lt;em&gt;Staphylococcus aureus&lt;/em&gt; 18mm compared to positive control chloramphenicol (24mm). 13mm observed in &lt;em&gt;A. flavus&lt;/em&gt; and &lt;em&gt;A. ochraceous&lt;/em&gt; where positive control streptomycin exhibits 18mm. GC-MS analysis revealed the presence of three major compounds in 8&amp;alpha; (2H)-Phenanthrenol, 7-ethenyldodecahydro-1,1,4&amp;alpha;, 7-tetramethyl-, acetate, [4&amp;alpha;s(4&amp;alpha;&amp;alpha;, 4b&amp;alpha;, 7&amp;alpha;, 8&amp;alpha;&amp;alpha;, 10&amp;alpha;&amp;alpha;)], Benzoic acid, 4-methyl- , 2-oxo-2- phenylethyl ester and Cyclohexanol, 5-methyl-2-(1-methylethyl)-, [1S-(1&amp;alpha;,2&amp;alpha;,5&amp;alpha;)] in the crude extracts. The preparative HPLC analysis proved the presence of single peak from the crude flavonoid compounds, where the absorption maximum was between 207-290nm exhibited by the UV spectrum analysis. FTIR spectrum confirmed the presence of amide group, phenol group, carboxylic acid, alkynyl, alkene and aromatic ring. NMR studies proved the presence of phenyl group, methyl group and H&lt;sub&gt;2&lt;/sub&gt;C-CH group and their molecular weight recorded as 353 through the mass spectrum analysis. &lt;strong&gt;Conclusion:&lt;/strong&gt; The identified compound considered as the vital compound to design the &amp;ldquo;green antimicrobial drugs&amp;rdquo;.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1208</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Tamilarasan Tamil Kumar&lt;sup&gt;1&lt;/sup&gt;, Seeni Mohamed Salique&lt;sup&gt;1&lt;/sup&gt;, Mohamed Hussain Muhammad Ilyas&lt;sup&gt;1&lt;/sup&gt;, Nooruddin Thajuddin&lt;sup&gt;2&lt;/sup&gt;, Annamalai Panneerselvam&lt;sup&gt;3&lt;/sup&gt;, Mohamed Khan Syed Ali Padusha&lt;sup&gt;4&lt;/sup&gt;, Hussain Syed Jahangir&lt;sup&gt;1,&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Post Graduate and Research Department of Botany, Jamal Mohamed College (Autonomous), Tiruchirappalli-620020, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Microbiology, School of Life Sciences, Bharathidasan University, Tiruchirappalli-620024, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Post Graduate and Research Department of Botany and Microbiology, A. Veeriya Vandayar Memorial Sri Pushpam College (Autonomous), Poondi-613503, Thanjavur District, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Post Graduate and Research Department of Chemistry, Jamal Mohamed College (Autonomous), Tiruchirappalli-620020, Tamil Nadu, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ade Arsianti</style></author><author><style face="normal" font="default" size="100%">Yully Astika Nugrahayning Aziza</style></author><author><style face="normal" font="default" size="100%">Kartika Dwi Kurniasari</style></author><author><style face="normal" font="default" size="100%">Baiq Kirana Dyahningrum Mandasari</style></author><author><style face="normal" font="default" size="100%">Riathul Masita</style></author><author><style face="normal" font="default" size="100%">Futihati Ruhama Zulfa</style></author><author><style face="normal" font="default" size="100%">Micheylla Kusumaning Dewi</style></author><author><style face="normal" font="default" size="100%">Cut Raisya Zahira Zagloel</style></author><author><style face="normal" font="default" size="100%">Norma Nur Azizah</style></author><author><style face="normal" font="default" size="100%">Rista Putrianingsih</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Test and Cytotoxic Activity of Macroalgae Eucheuma cottonii against Cervical HeLa Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-cervical cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Eucheuma cottonii</style></keyword><keyword><style  face="normal" font="default" size="100%">HeLa cell lines</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical test</style></keyword><keyword><style  face="normal" font="default" size="100%">Seaweed</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">1012-1017</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Intoduction:&lt;/strong&gt; Marine resource of macroalgae &lt;em&gt;Eucheuma cottonii&lt;/em&gt; from East Lombok, Nusa Tenggara Barat, Indonesia, have potential as anti-cervical cancer agent. &lt;strong&gt;Objectives:&lt;/strong&gt; Finding cytotoxic activity of &lt;em&gt;Eucheuma cottonii&lt;/em&gt; hexane, ethylacetate, chloroform and ethanol extracts against cervical HeLa cells by MTT cell proliferation assay. &lt;strong&gt;Methods:&lt;/strong&gt; The extracts was tested in phytochemical and cytotoxic activity test. Phytochemical test to identify composition of secondary metabolite such as flavonoid, alkaloid, saponins, tannin, triterpenoid, steroid and glycoside. The amount of substances contained in the extract sample was analyzed by Thin Layer Chromatography (TLC). Cytotoxic activity using HeLa cells. Results: Phytochemical test of &lt;em&gt;E. cottonii&lt;/em&gt; extracts showed the positive result for metabolite of flavonoid, whereas the TLC analysis revealed that the extracts containing five chemical compounds. Ethanol, n-hexane, chloroform, and ethyl acetate extracts of &lt;em&gt;E. cottonii&lt;/em&gt; exhibited a strong cytotoxic activity against cervical HeLa cells with IC&lt;sub&gt;50&lt;/sub&gt; of 7.54 &amp;mu;g/mL, 5.73 &amp;mu;g /mL, 4.82 &amp;mu;g /mL and 4.34 &amp;mu;g / mL, respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; The results suggest that macroalgae &lt;em&gt;Eucheuma cottonii&lt;/em&gt; could be used as a new anti-cervical cancer&amp;rsquo;s candidate.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1012</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ade Arsianti&lt;sup&gt;1,2,*&lt;/sup&gt;, Yully Astika Nugrahayning Aziza&lt;sup&gt;3&lt;/sup&gt;, Kartika Dwi Kurniasari&lt;sup&gt;3&lt;/sup&gt;, Baiq Kirana Dyahningrum Mandasari&lt;sup&gt;3&lt;/sup&gt;, Riathul Masita&lt;sup&gt;3&lt;/sup&gt;, Futihati Ruhama Zulfa&lt;sup&gt;3&lt;/sup&gt;, Micheylla Kusumaning Dewi&lt;sup&gt;3&lt;/sup&gt;, Cut Raisya Zahira Zagloel&lt;sup&gt;3&lt;/sup&gt;, Norma Nur Azizah&lt;sup&gt;2&lt;/sup&gt;, Rista Putrianingsih&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Medical Chemistry, Faculty of Medicine, University of Indonesia, Jakarta, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Drug Development Research Cluster, Indonesia Medical Education and Research Institute (IMERI), Faculty of Medicine, University of Indonesia, Jalan Salemba Raya 6 Jakarta 10430, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Medical Student, Faculty of Medicine University of Indonesia, Depok, INDONESIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Robert Hotman Sirait</style></author><author><style face="normal" font="default" size="100%">Mochammad Hatta</style></author><author><style face="normal" font="default" size="100%">Syafri K.Arief</style></author><author><style face="normal" font="default" size="100%">Tigor P. Simanjuntak</style></author><author><style face="normal" font="default" size="100%">Bambang Suprayogi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Profile of HMGB1 mRNA Expression and TLR4 Protein in BALB/c Mice Model Sterile Injury after Systemic Lidocaine Administration</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">HMGB1 mRNA</style></keyword><keyword><style  face="normal" font="default" size="100%">lidocaine</style></keyword><keyword><style  face="normal" font="default" size="100%">Sterile injury</style></keyword><keyword><style  face="normal" font="default" size="100%">TLR4</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/529</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">586-589</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; High mobility group box 1 (HMGB1) is a cytokine proinflamation which contributes to inflammation. HMGB1 physically interacts with toll like receptor 4 (TLR4) to release macrophage cytokines. The aim of this study was to demonstrate the effectiveness of systemic lidocaine administration to inhibit the expression of HMGB1 mRNA and TLR4 protein in mice BALB/c mice with sterile injury. &lt;strong&gt;Material and Methods:&lt;/strong&gt; Twenty adult male BALB/c mice were divided into lidocaine and control groups. A sterile injury is done by closed fracturing the left thigh bone of the mice. The lidocaine group was treated with 2 mg/kgBW lidocaine through tail vein injection after 4 h of sterile injury. The control group was given distilled water therapy as a substitute for lidocaine. Mice blood is extracted from the tail vein before trauma, 4 h after trauma, and 2 h after the administration of lidocaine and distilled water is complete. The HMGB1 mRNA expression was examined by quantitative real-time polymerase chain reaction (qPCR) while the TLR4 protein level was determined with enzyme-linked immunosorbent assay (ELISA) according to the manufacturer&amp;rsquo;s instructions. &lt;strong&gt;Result:&lt;/strong&gt; The HMGB1 mRNA expression and TLR4 protein levels in BALB/c that sustained inflammation due to a sterile injury was significantly decreased in the lidocaine group (&lt;em&gt;p&lt;/em&gt; &amp;lt; 0.00). &lt;strong&gt;Conclusion:&lt;/strong&gt; Administration systemic 2 mg/kgBW of lidocaine is effectively inhibits HMGB1 mRNA and TLR4 protein in mice that sustain inflammation due to a sterile injury.&amp;nbsp;&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">586</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Robert Hotman Sirait&lt;sup&gt;1&lt;/sup&gt;, Mochammad Hatta&lt;sup&gt;2&lt;/sup&gt;, Syafri K.Arief&lt;sup&gt;3&lt;/sup&gt;, Tigor P. Simanjuntak&lt;sup&gt;4&lt;/sup&gt;, Bambang Suprayogi&lt;sup&gt;5&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Anesthesiology, Faculty of Medicine, Christian University of Indonesia, Jakarta, Indonesia&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Molecular Biology and Immunology Laboratory, Faculty of Medicine, University of Hasanuddin, Makassar, Indonesia&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Anesthesiology, Faculty of Medicine, University of Hasanuddin, Makassar, Indonesia&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Obstetric and Gynecology, Faculty of Medicine, Christian University of Indonesia, Jakarta, Indonesia&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Otorhinolaryngology, Faculty of Medicine, Christian University of Indonesia, Jakarta, Indonesia&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aswathy Jayasree Madanakumar</style></author><author><style face="normal" font="default" size="100%">Bosco Lawarence</style></author><author><style face="normal" font="default" size="100%">Manoj GS</style></author><author><style face="normal" font="default" size="100%">Murugan Kumaraswamy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Purified Anthocyanin from in vitro Culture of Bridelia retusa (L.) Spreng. Capable of Inhibiting the Growth of Human Oral Squamous Cell Carcinoma Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anthocyanin</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-metastatic potential</style></keyword><keyword><style  face="normal" font="default" size="100%">Apoptosis</style></keyword><keyword><style  face="normal" font="default" size="100%">Bridelia retusa</style></keyword><keyword><style  face="normal" font="default" size="100%">Cell suspension</style></keyword><keyword><style  face="normal" font="default" size="100%">in vitro culture</style></keyword><keyword><style  face="normal" font="default" size="100%">Purification</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/524</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">559-566</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;The present study aims &lt;em&gt;in vitro&lt;/em&gt; cell suspension culture of &lt;em&gt;Bridelia retusa&lt;/em&gt;, isolation of anthocyanin, purification, fractionation and its anti-metastatic potential against oral squamous carcinoma cells. Experimental results reveal that 2, 4-D either alone or in combination with kinetin supplemented in MS medium showed significant initiation of callus from leaf explants than stem. Growth hormones, pH, light, and carbon source influence anthocyanin synthesis. Maximum callus induction was noticed with 2.5 mg/L N6-benzyladenine (BA) + 2 mg/L 2, 4-dichlorophenoxyacetic acid (2, 4-D) (98.9%). Fresh and dry weight of the calli were i.e., 1.9 &amp;plusmn; 0.04 and 0.45 &amp;plusmn; 0. 03 g respectively. Optimal response was seen with light on MS medium contain 4% glucose + 2.5 mg/L BA and 2 mg/L 2, 4-D at pH 3.5 yielded 2.8 mg /g of anthocyanins. Suspension culture medium fortified with 2, 4-D (2.5 mg/L) + BA (2 mg/L) at pH 5.0 induced anthocyanin production at pH 4.4 &amp;ndash; 4.6. HCl-ethanol extraction for 90 min yielded the maximum anthocyanin content. Fractionation of anthocyanin using HPLC coupled with mass spectrometry revealed 07 fractions such as acylated cyanidins, two peonidins, cyanidin 3-p-coumaroyl and feruloyl diglucoside-5-glucosides. In the search of novel therapeutic drugs against cancer, cytotoxicity effect of &lt;em&gt;B.retusa&lt;/em&gt; anthocyanin extracts on human oral squamous cell carcinoma (SCC4, SCC9 and SCC25) cells using cell adhesion and cell viability assay was carried. The morphological alterations in SCCs cells after treatment with &lt;em&gt;B.retusa&lt;/em&gt; anthocyanin includes nuclear condensation, fragmentation and apoptotic cells as revealed by Hoechst stain. Flow cytometry showed arresting of SCC25 cells mostly in the G0/G1 and S-G2/M stages with a concomitant up regulation of sub-G1 fraction, indicating cell death by apoptosis. Apoptosis was further substantiated by the activation of caspase-3 expression in the SCC25 cells treated with &lt;em&gt;B.retusa&lt;/em&gt; anthocyanin. Thus, it is possible to suggest that &lt;em&gt;B.retusa&lt;/em&gt; anthocyanin cause apoptosis of SCCs and warrant further investigation using animal models.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">559</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aswathy Jayasree Madanakumar&lt;sup&gt;1&lt;/sup&gt;, Bosco Lawarence&lt;sup&gt;2&lt;/sup&gt;, Manoj GS&lt;sup&gt;3&lt;/sup&gt;,Murugan Kumaraswamy&lt;sup&gt;1*&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Botany, Plant Biochemistry and Molecular biology Laboratory, University College, Thiruvananthapuram, Kerala- 695 034, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Botany and Biotechnology, Govt. Arts College, Trivandrum-14, Kerala, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Botany, Nilamel NSS College, Kerala, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aswathy Jayasree Madanakumar</style></author><author><style face="normal" font="default" size="100%">Murugan Kumaraswamy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Purified Anthocyanin, its Elicitation from Cell Cultures of Begonia malabarica and Begonia rex-cultorum ‘Baby Rainbow’and it’s In vitro Cytotoxicity Analysis by MTT Assay</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anthocyanin</style></keyword><keyword><style  face="normal" font="default" size="100%">Begonia</style></keyword><keyword><style  face="normal" font="default" size="100%">Cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Cell suspension.</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">MTT Assay</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/523</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">553-558</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; According to recent statistics, cancer accounts about marked percentage of total deaths in the world, although there are many therapeutic approaches. Unfortunately, the cytotoxicity properties of most chemotherapy drug are nonspecific and therefore do not distinguish between normal healthy cells and tumor cells, these events have led to inappropriate and toxic therapeutic agents with a wide range of side effects. However, several experimental and epidemiological studies have suggested that fruits and vegetables are associated with low risk of various types of cancer. Anthocyanins are natural pigments that provide intense purple to red color in plants. Anthocyanin possess the ability to inhibit oxidative stress and to induce apoptosis in malignant cells, thus may prevent carcinogenesis. &lt;strong&gt;Methods:&lt;/strong&gt; Antiproliferative properties of purified anthocyanin extract from elicited cell suspension cultures of &lt;em&gt;Begonia malabarica&lt;/em&gt; and &lt;em&gt;Begonia rex-cultorum&lt;/em&gt; &amp;lsquo;Baby rainbow&amp;rsquo; was investigated in terms of MTT assay. Anthocyanin extracts were tested for their ability to inhibit the growth of HT29 (colon cancer cells), MG63 (Osteosarcoma), HeLa (Cervical cancer cells) and L929 (Mouse Fibroblast L929) cell lines. &lt;strong&gt;Results:&lt;/strong&gt; Cell viability decreased in a dose dependent manner in all the considered cell lines treated with anthocyanin extracts. The extract of &lt;em&gt;Begonia rex-cultorum&lt;/em&gt; &amp;lsquo;Baby rainbow&amp;rsquo; exhibited significant cytotoxic activity against all tumor cell lines than &lt;em&gt;Begonia malabarica&lt;/em&gt; extract. &lt;em&gt;Begonia malabarica&lt;/em&gt; and &lt;em&gt;Begonia rex-cultorum&lt;/em&gt; &amp;lsquo;Baby rainbow&amp;rsquo; anthocyanin extract exhibited the highest cytotoxicity towards HT29 and HeLa cell lines respectively. But, MG63 resulted in comparatively higher percentage of viability of cell lines at the same concentrations. The anthocyanin extract produced significant morphological alterations on cell lines in culture. Meanwhile, the extracts showed poor cytotoxicity against the normal cell line. &lt;strong&gt;Conclusion:&lt;/strong&gt; The morphological alteration of the treated cancer cells presented clear evidence of significant cytotoxicity of anthocyanin extracts of both Begonias in all the three cell lines. Thus, anthocyanin may act as chemopreventive agents for various cancer cell lines.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">553</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aswathy Jayasree Madanakumar, Murugan Kumaraswamy&lt;sup&gt;* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Plant Biochemistry and Molecular Biology Laboratory, Department of Botany, University College, Trivandrum, 695 034, Kerala, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ridzwan Norhaslinda</style></author><author><style face="normal" font="default" size="100%">Jumli Mimie Noratiqah</style></author><author><style face="normal" font="default" size="100%">Baig Atif Amin</style></author><author><style face="normal" font="default" size="100%">Rohin Mohd Adzim Khalili</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Quantitative and Optimization of Anthocyanin Extracted from Pomegranate (Punica Granatum) Extract by High-Performance Liquid Chromatography (HPLC)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">5-diglucoside</style></keyword><keyword><style  face="normal" font="default" size="100%">Cyanidin 3</style></keyword><keyword><style  face="normal" font="default" size="100%">Cyanidin 3-glucoside</style></keyword><keyword><style  face="normal" font="default" size="100%">Pelargonidin 3</style></keyword><keyword><style  face="normal" font="default" size="100%">Pelargonidin 3-glucoside</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/645</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">650-653</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; &lt;em&gt;P. granatum&lt;/em&gt; is one of the oldest edible fruits of tropical and subtropical regions. This fruit had high antioxidant contained by hydrolysable tannins and anthocyanin compounds that give many health benefit properties. This study aims to quantify and optimized anthocyanin from &lt;em&gt;P. granatum&lt;/em&gt; extract. &lt;strong&gt;Methods:&lt;/strong&gt; A total of 50g of the flesh was soaked into two different polar solvents; water and 50% ethanol within a ratio of 1:10; w/v for 24-hr. Then, three different methods of extraction were done and test each with HPLC analytical, respectively. &lt;strong&gt;Results:&lt;/strong&gt; The validated method proved to be linear in the range of 5 &amp;ndash; 30 ug/mL and with LOD and LOQ determined respectively for Cy3, Cy3, 5, Pg3, and Pg3, 5. The method also shows recovery (%) close to 100 when accuracy was accessed. For samples, blender water extract had a higher composition of Cy3, Cy3, 5 and Pg3, 5 (22.77 &amp;plusmn; 8.82 mg/100 g e.p; 25.36 &amp;plusmn; 9.95 mg/100 g e.p; 11.16 &amp;plusmn; 5.85 mg/100 g e.p) content as compared to other. &lt;strong&gt;Conclusion:&lt;/strong&gt; As a conclusion, the present methodology proved to be capable of detecting and quantifying Cy3, Cy3, 5, Pg3, Pg3, 5 in a single run. Also, comparatively the composition of each AC detected in blender water extract is significantly higher in value than the other methods. It should regard as a valuable source of antioxidant with the potential used for health benefits properties worldwide.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">650</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ridzwan Norhaslinda&lt;sup&gt;1&lt;/sup&gt;, Jumli Mimie Noratiqah&lt;sup&gt;1&lt;/sup&gt;, Baig Atif Amin&lt;sup&gt;2&lt;/sup&gt;, Rohin Mohd Adzim Khalili&lt;sup&gt;1,3,4&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;School of Nutrition and Dietetic, Faculty of Health Sciences, University Sultan Zainal Abidin (UniSZA), Gong Badak Campus, Kuala Nerus, Terengganu, MALAYSIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Medicine, University Sultan Zainal Abidin, Medical Campus, Jalan Sultan Mahmud, Kuala Terengganu, Terengganu Darul Iman, MALAYSIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Centre for Continuing Education (CCE), Universiti Sultan Zainal Abidin (UniSZA), Gong Badak Campus, 21300 Kuala Nerus, Terengganu, MALAYSIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Institute for Community (Health) Development, Universiti Sultan Zainal Abidin (UniSZA), Gong Badak Campus, 21300 Kuala Nerus, Terengganu, MALAYSIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jumli Mimie Noratiqah</style></author><author><style face="normal" font="default" size="100%">Ridzwan Norhaslinda</style></author><author><style face="normal" font="default" size="100%">Baig Atif Amin</style></author><author><style face="normal" font="default" size="100%">Rohin Mohd Adzim Khalili</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Quantitative and Optimization of Phenolic Acid Extracted from Pomegranate by High Performance Liquid Chromatography (HPLC)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Caffeic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Ellagic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Ferulic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Gallic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Pomegranate extract</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">969-972</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; Pomegranate is scientifically known as &lt;em&gt;Punica granatum&lt;/em&gt; L. which is a nutrient dense fruit rich in phytochemical compounds. Phenolic content is the main compound attribute for the most of the functional properties in pomegranate. The aim of this study is to quantify and optimize the composition of phenolic acids extracted from pomegranate extract by using High-performance Liquid Chromatography (HPLC). &lt;strong&gt;Method:&lt;/strong&gt; The pomegranate extracted with three different methods by using two different solvents which is 50% ethanol and water. The methods were blended (aril+ seed), Soaking (aril+ seed) and soaking + squeezed manually. HPLC-PDA was used as equipment to quantify and optimize the phenolic acids extracted from pomegranate. Result: Validation method of HPLC was analysed according to the percentage of recovery, LOD, LOQ and coefficient correlation. Result showed that GA was detected in all sample from different method of extraction applied while CA compound not detected in any of extraction method applied. FA compound was only detected in blended method by 50% ethanol and water as solvent while EA compound was detected only in water extraction of all three methods applied. &lt;strong&gt;Conclusion:&lt;/strong&gt; As a conclusion, according to the standard calibration data curve showed that this method proved to detect and quantify the targeted compounds. By comparing the data obtained from this study, it showed that water blended extract method is significantly higher content of targeted compound except for the CA compound. To the best of our knowledge, this sample can be a valuable source of antioxidant for better used in health benefits.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">969</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Jumli Mimie Noratiqah&lt;sup&gt;1&lt;/sup&gt;, Ridzwan Norhaslinda&lt;sup&gt;1&lt;/sup&gt;, Baig Atif Amin&lt;sup&gt;2&lt;/sup&gt;, Rohin Mohd Adzim Khalili&lt;sup&gt;1,3,4* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;School of Nutrition and Dietetic, Faculty of Health Sciences, Universiti Sultan Zainal Abidin (UniSZA), Gong Badak Campus, 21300 Kuala Nerus, Terengganu, MALAYSIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Medicine, Universiti Sultan Zainal Abidin (UniSZA), Medical Campus, Jalan Sultan Mahmud, 20400 Kuala Terengganu, Terengganu, MALAYSIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Centre for Continuing Education (CCE), Universiti Sultan Zainal Abidin (UniSZA), Gong Badak Campus, 21300 Kuala Nerus, Terengganu, MALAYSIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Institute for Community (Health) Development, Universiti Sultan Zainal Abidin (UniSZA), Gong Badak Campus, 21300 Kuala Nerus, Terengganu, MALAYSIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Noha A Khalil</style></author><author><style face="normal" font="default" size="100%">Amira Abdel Motaal</style></author><author><style face="normal" font="default" size="100%">Khaled Meselhy</style></author><author><style face="normal" font="default" size="100%">Soad M Abdel khalek</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Renin and Angiotensin Converting Enzyme Inhibition of Standardized Bioactive Fractions of Hyphaene thebaica L. Mart Growing in Egypt</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antihypertensive</style></keyword><keyword><style  face="normal" font="default" size="100%">Doum</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolics</style></keyword><keyword><style  face="normal" font="default" size="100%">standardization</style></keyword><keyword><style  face="normal" font="default" size="100%">Validation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/640</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">622-627</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Hyphaene thebaica&lt;/em&gt; L. fruit is known in Egypt for its antihypertensive activity. However a standardized herbal extract/fraction was never prepared.&lt;strong&gt; Methods:&lt;/strong&gt; A biologically guided fractionation was carried out &lt;em&gt;in-vitro&lt;/em&gt; for the 50% and 70% ethanol extracts of &lt;em&gt;Hyphaene thebaica&lt;/em&gt; L. fruit using the angiotensin converting enzyme (ACE) inhibition and renin inhibition assays. A validated reversed phase HPLC method was developed for the standardization of the active fractions. Results: The ethyl acetate fraction of the 70% extract contained higher percentages of the three bioactive markers chlorogenic acid, quercetin and apigenin (1.940 &amp;plusmn; 0.140%, 2.994 &amp;plusmn; 0.349% and 0.612 &amp;plusmn; 0.0354%, respectively) relative to the ethyl acetate fraction of the 50% extract (1.384 &amp;plusmn; 0.157%, 0.342 &amp;plusmn; 0.0834% and 0.070 &amp;plusmn; 0.00225%, respectively). The butanol fraction of the 70% extract was found to possess the highest antihypertensive activity (93.69 &amp;plusmn; 5.695 % renin inhibition activity at 0.5 mg/mL and IC&lt;sub&gt;50&lt;/sub&gt; of 0.001436 +0.00044 mg/mL for ACE inhibition activity). A standard calibration curve for the three compounds was established at a concentration range of 0.1-50 &amp;mu;g/Ml, they showed good linearity with a correlation coefficient (R&lt;sup&gt;2&lt;/sup&gt;) of (1.00, 1.00 and 0.999; respectively). A high degree of precision (relative standard deviation values &amp;lt;5%) was achieved. The limits of detection for the three compounds were 0.428, 0.368 and 0.849; respectively, while the limits of quantitation were 1.29, 1.11 and 2.57, respectively. &lt;strong&gt;Conclusions:&lt;/strong&gt; Current results showed that the butanol fraction of the 70% extract revealed the highest antihypertensive activity through ACE and renin inhibition mechanisms. In addition, recorded observations concerning linearity of the used bioactive markers offer a support for the possible utility of the tested fractions as potent standardized antihypertensive drugs.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">622</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Noha A Khalil&lt;sup&gt;1*&lt;/sup&gt;, Amira Abdel Motaal&lt;sup&gt;2,3&lt;/sup&gt;, K M Meselhy&lt;sup&gt;3&lt;/sup&gt;, Soad M Abdel Khalek&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;4&lt;/strong&gt; &lt;/sup&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Faculty of Pharmacy, Misr International University, EGYPT.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacognosy, College of Pharmacy, King Khaled University, Abha, KINGDOM OF SAUDI ARABIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, EGYPT.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacognosy, Faculty of Pharmacy, Nahda University, BeniSuef, Helwan University, EGYPT.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prasad Kadam</style></author><author><style face="normal" font="default" size="100%">Manohar Patil</style></author><author><style face="normal" font="default" size="100%">Kavita Yadav</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Review on Phytopharmacopial Potential of Epilobium angustifolium</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biological activities</style></keyword><keyword><style  face="normal" font="default" size="100%">Epilobium angustifolium L</style></keyword><keyword><style  face="normal" font="default" size="100%">Herbaceous</style></keyword><keyword><style  face="normal" font="default" size="100%">Oenothein B</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacological Effects</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">1076-1078</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;Nature has been a source of medicinal agents for thousands of years, and an impressive number of modern drugs have been isolated from natural sources which are based on their use in traditional medicine.&lt;em&gt; Epilobium angustifolium&lt;/em&gt; L is a perennial herbaceous plant that belongs to the &lt;em&gt;Onagraceae&lt;/em&gt; family. It exhibits various therapeutic properties like anticancer, antibacterial, anti-inflammatory, antioxidant, and anti-aging properties. &lt;em&gt;Epilobium angustifolium&lt;/em&gt; L. contains polyphenols and secondary metabolites like oenothein B. Information was collected via Medline, PubMed, and Science Direct. Also some data have been collected from scientific journals, books, and reports. This review gives the current information on the chemical composition, traditional uses, and documented biological activities of &lt;em&gt;Epilobium angustifolium&lt;/em&gt; L. These studies reveal that &lt;em&gt;Epilobium&lt;/em&gt; &lt;em&gt;angustifolium&lt;/em&gt; L is a source of medicinally active compounds and have various pharmacological effects. These studies will be helpful to create interest toward&lt;em&gt; Epilobium angustifolium&lt;/em&gt; L and may be useful in developing a new direction for further research.&lt;em&gt;Epilobium angustifolium&lt;/em&gt; L.is a medicinally important plant belongs to &lt;em&gt;Onagraceae&lt;/em&gt; family. Extract from the plant is used in the treatment of many diseases for its anti-tumor, antimicrobial, anti-inflammatory, antioxidant, anti-ulcer and many other properties. The medicinal properties of fireweed have been attributed to its high content in polyphenols and more particularly to the most abundant of its secondary metabolites: Oenothein B.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">1076</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Prasad Kadam&lt;sup&gt;1&lt;/sup&gt;*,&amp;nbsp;Manohar Patil&lt;sup&gt;2&lt;/sup&gt;,&amp;nbsp;Kavita Yadav&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Associate Professor, Marathwada Mitra Mandal&amp;rsquo;s College of Pharmacy, Pune- 411033, Maharashtra, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacognosy, Principal and Professor of Pharmacognosy, Marathwada Mitra Mandal&amp;rsquo;s College of Pharmacy, Pune-411033, Maharashtra, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Asser Ashraf Ahmad</style></author><author><style face="normal" font="default" size="100%">Ihab Ibrahim Al Khalifa</style></author><author><style face="normal" font="default" size="100%">Zead Helmi Abudayeh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Role of Pomelo Peel Extract for Experimentally Induced Wound in Diabetic Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Peel</style></keyword><keyword><style  face="normal" font="default" size="100%">Pomelo</style></keyword><keyword><style  face="normal" font="default" size="100%">Vitamin C</style></keyword><keyword><style  face="normal" font="default" size="100%">Wound</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">885-891</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Delayed wound healing is a chronic complication in diabetic patients than in healthy individuals. Pomelo belongs to the genus Citrus of the family Rutaceae, an important fruit with great benefits for humans in the world. Previous studies showed that pomelo peels contain an abundant bioactive compound, which may promote wound healing in experimental animals. &lt;strong&gt;Aim:&lt;/strong&gt; The current study was carried to prepare optimized extraction of pomelo peels using different experimental conditions and investigate the possible healing effect of oral treatment with pomelo peel extract (PPE) on induced excision skin wound in diabetic rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; This study was done on rats divided into five groups each of 8 rats (two treatment groups given PPE (400 and 600) mg/kg by oral gavage compared to two control groups and standard plant for wound healing). Diabetes was induced by intraperitoneal injection of a single dose of Streptozotocin (STZ) 65 mg\kg body weight. After diabetes induction, full thickness excision wound was made in rats, and the study continued for 3 weeks.&lt;strong&gt; Results:&lt;/strong&gt; This study showed significant reduction in blood glucose and both percentage and time to wound closure in the treated groups, also a significant increase in hydroxyproline and total protein content of the healed wound tissue in the treated groups compared with control groups and comparable to standard plant extract treated groups. &lt;strong&gt;Conclusion:&lt;/strong&gt; Experimental data proposed that oral administration of pomelo peel extract rich in vitamins and flavonoids has a good therapeutic potential in the treatment of complicated wounds in diabetes.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">885</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Asser Ashraf Ahmad&lt;sup&gt;1&lt;/sup&gt;, Ihab Ibrahim Al Khalifa&lt;sup&gt;2&lt;/sup&gt;, Zead Helmi Abudayeh&lt;sup&gt;3&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacy Science / pharmacology /Applied Pharmaceutical Science and Clinical Pharmacy/ Faculty of Pharmacy, Al-Isra University, Amman, JORDAN.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology and Toxicology/Pharmacy/AL-Rasheed University, Baghdad, IRAQ.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Pharmaceutical Chemistry and Pharmacognosy/ Applied Pharmaceutical Science and Clinical Pharmacy Department / Faculty of Pharmacy, Al-Isra University, Amman, JORDAN.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veeraprakash Bathini</style></author><author><style face="normal" font="default" size="100%">Suresh Kumar Kalakandan</style></author><author><style face="normal" font="default" size="100%">Muthukumaran Pakkirisamy</style></author><author><style face="normal" font="default" size="100%">Karthikeyen Ravichandran</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Structural Elucidation of Peanut, Sunflower and Gingelly Oils by Using FTIR and 1H NMR Spectroscopy</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">1H-NMR</style></keyword><keyword><style  face="normal" font="default" size="100%">FTIR</style></keyword><keyword><style  face="normal" font="default" size="100%">TAG</style></keyword><keyword><style  face="normal" font="default" size="100%">Unsaturation</style></keyword><keyword><style  face="normal" font="default" size="100%">WHO</style></keyword><keyword><style  face="normal" font="default" size="100%">Z-Conformation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/664</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">753-757</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aims:&lt;/strong&gt; The present study focused on FTIR and &lt;sup&gt;1&lt;/sup&gt;H-NMR spectroscopic methods to assign structural connectivity and purity of the oils. &lt;strong&gt;Methods:&lt;/strong&gt; Non-destructive Fourier Transform Infrared (FTIR) and &lt;sup&gt;1&lt;/sup&gt;H nuclear magnetic resonance (&lt;sup&gt;1&lt;/sup&gt;H-NMR) spectroscopy techniques are used to assign the structural confirmation of the triacylglyceride (TAG) functional component in three different oils namely Sunflower, Peanut, and Gingelly oils respectively. &lt;strong&gt;Results:&lt;/strong&gt; FTIR spectrum shows a very high intense band at 1744 cm&lt;sup&gt;-1&lt;/sup&gt; associated with the existence of the ester carbonyl functional group (O-C=O) and very weak shoulder peak of cis double-bond (C=C) stretching was noticed at &amp;sim;1655 cm&lt;sup&gt;-1&lt;/sup&gt;. In &lt;sup&gt;1&lt;/sup&gt;H-NMR spectrum shows well resolved chemical shift values in the range 5.3-0.8 ppm corresponding to characteristic group in aliphatic region. &lt;strong&gt;Conclusion:&lt;/strong&gt; Each distinct peak was determined based on chemical shift as well as splitting pattern values. For olefin signal as triplet, tertiary methine protons as singlet, well separated oxymethylene seen as triplet at ~4.2 ppm owing to presence of high electronegative oxygen atom connected to methylene chain gives more deshielding effect. As for bis-allylic, &amp;alpha;-carbonyl methylene, &amp;beta;-carbonyl methylene, allylic, saturated methylene along with terminal methyl proton signals are noticed in the span of 2.3-0.8 ppm. A remarkable feature of the spectra is well resolved chemical shift values is clearly support presence of longer hydrocarbon chains. Absence of multiplet coupling peaks and disappearance of signals in down shield region &amp;gt; 5.4 ppm confirms the absence of trans stereoisomer (E-conformation), aromatic and heterocyclic epoxide compounds.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">753</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Veeraprakash Bathini, Suresh Kumar Kalakandan&lt;sup&gt;*&lt;/sup&gt;, Muthukumaran Pakkirisamy,&amp;nbsp;Karthikeyen Ravichandran &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Food Safety Quality Testing Laboratory, Indian Institute of Food Processing Technology, Thanjavur, Tamil Nadu, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Paranthaman Ramakrishnan</style></author><author><style face="normal" font="default" size="100%">Sureshkumar Kalakandan</style></author><author><style face="normal" font="default" size="100%">Muthukumaran Pakkirisamy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Studies on Positive and Negative ionization mode of ESI-LC-MS/ MS for screening of Phytochemicals on Cassia auriculata (Aavaram Poo)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Caucalis platycarpos L.; Methanol</style></keyword><keyword><style  face="normal" font="default" size="100%">Eelectrospray ionization</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoids; UHPLCESI- MS</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/508</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">457-462</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Cassia auriculata&lt;/em&gt; (Avaram) is an important medicinal plant in India Improved awareness in medicinal flowers has led to an increased need for efficient extraction methods and screening of flavonoid derivatives. &lt;strong&gt;Objective:&lt;/strong&gt; To standardization of extraction solvent system and Characterization of flavonoids through positive and negative electrospray ionization mode using LC-MS/MS from &lt;em&gt;Cassia auriculata&lt;/em&gt; extract. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The different solvents like Methanol, Water, Acetonitrile, Ethyl Acetate, Ethanol, Chloroform, Hexane, Acetone Diethyl ether used frot he identification of flavonoids (Gallic acid, Theanine, Theobromine, Theophylline, Caffeic acid, Caffeine, Ferulic acid, Theacrine, Catechin, Quercetin, EpiGallo Catachin, catechin gallate, Epicatachin gallate and Quercetin hexoside. &lt;strong&gt;Results:&lt;/strong&gt; Based on the peak area percentage the extraction solvent was standardized. The percentage of relative &amp;amp; absolute intensity of screened flavonoids was observed using LC-MS in positive and negative electrospray ionization. The results show that the methanol extract has more percentage of peak area, relative intensity and absolute intensity. The MS results showed that the negative ionoization has more intensity values of flavonoids and the signal-to-noise ratio was high in negative ionization mode compare to positive mode. &lt;strong&gt;Conclusion:&lt;/strong&gt; Based on the results the methanol is the suitable extraction solvetnt and negative ionization mode of ESI-LC-MS/MS was appropriate for the screening of flavonoids on &lt;em&gt;Cassia auriculata&lt;/em&gt; flower extracts.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">457</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Paranthaman Ramakrishnan, Sureshkumar Kalakandan&lt;sup&gt;*&lt;/sup&gt;, Muthukumaran Pakkirisamy &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;(NABL Accredited and&amp;nbsp;FSSAI Referral lab) Indian Institute of Food Processing Technology (IIFPT), Ministry of Food Processing Industries, Govt. of India, Thanjavur-613 005, Tamil Nadu, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Suma Krishnaswamy</style></author><author><style face="normal" font="default" size="100%">Bopaiah A Kushalappa</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Systematic Review and Meta-analysis of Andrographis serpyllifolia (Rottler ex Vahl) Wight: An Ethno-pharmaco- botanical Perspective</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Andrographis serpyllifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">Botanical aspects</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethnobotany</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacological screening</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical screening</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">s14-s26</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;em&gt;Andrographis serpyllifolia&lt;/em&gt; (Rottler ex Vahl) Wight, belonging to Acanthaceae, has been recorded in ethnobotanical archives as a plant possessing potent anti- snake and scorpion venom activity. Its leaf extract has been proven a highly effective drug to combat bovine mastitis. The present review compiles most of the available experimental data emphasising phytochemical profiles and the pharmacological actitvty of this medicinal geophyte. This kind of systematic review encompassing all experimentally proven aspects of the plant, gaps in research and potential areas for future investigation is not available in literature published with regard to this plant so far.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">s14</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Suma Krishnaswamy&lt;sup&gt;1*&lt;/sup&gt;, Bopaiah A Kushalappa&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Research and Development Centre, Bharathiar University, Department of Botany, Coimbatore &amp;ndash; 641046, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;St. Joseph&amp;rsquo;s College for Post Graduate Studies, Department of Botany Langford Road, Bangalore &amp;ndash; 560 027, Karnataka, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nandkishor Ramdas Kotagale</style></author><author><style face="normal" font="default" size="100%">Ankit Kedia</style></author><author><style face="normal" font="default" size="100%">Rupali Gite</style></author><author><style face="normal" font="default" size="100%">Shubham Nilkanth Rahmatkar</style></author><author><style face="normal" font="default" size="100%">Dinesh Yugraj Gawande</style></author><author><style face="normal" font="default" size="100%">Milind Janraoji Umekar</style></author><author><style face="normal" font="default" size="100%">Brijesh Gulabrao Taksande</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Withaferin A attenuates Alcohol Abstinence Signs in Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anxiety</style></keyword><keyword><style  face="normal" font="default" size="100%">Corticosterone</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethanol withdrawal</style></keyword><keyword><style  face="normal" font="default" size="100%">HPA axis</style></keyword><keyword><style  face="normal" font="default" size="100%">Withaferin A.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">August 2018</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">1190-1195</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Withania somnifera&lt;/em&gt; (WS) have been reported to inhibit acquisition and expression conditioned place preference, self-administration and withdrawal anxiety of psychostimulants. In the present work, we have assessed the effect of withaferin A on somatic and affective symptoms of ethanol withdrawal syndrome in rats. &lt;strong&gt;Methods:&lt;/strong&gt; Animals had given free access to ethanol uninterrupted for 21 days through liquid diet. Withaferin A (5, 10 and 20 mg/kg) was injected (ip) either during the development of ethanol dependence phase (days 15 &amp;ndash; 21 or 30 min before ethanol withdrawal assessment. Withdrawal signs characterized by changes in somatic signs were measured in the open field followed by evaluation of anxiety parameters, locomotion, and depressive behavior. &lt;strong&gt;Results:&lt;/strong&gt; Withaferin A treatment 30 min before 24 h postethanol withdrawal assessment did not alter the scores of somatic behavioral signs in ethanol abstinence animals. However, withaferin A (10 and 20 mg/kg, ip) from day 15-21 prevented the ethanol withdrawal-induced elevated scores of somatic behaviors, hyperlocomotion, depressive behavior, and anxiety. Withaferin A treatment did not influence the blood ethanol levels in dependent and withdrawn animals. However, withaferin A administration attenuated the elevated plasma corticosterone and ACTH levels in ethanol-withdrawn rats, suggesting withaferin A induced anti-stress effect and stabilization of HPA axis activity could have facilitated the inhibitory effect of withaferin A on ethanol withdrawal syndrome. &lt;strong&gt;Conclusion:&lt;/strong&gt; The finding supports further investigation of withaferin A and other bioactive components of WS in alcohol addiction.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1190</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Nandkishor Ramdas Kotagale, Ankit Kedia, Rupali Gite, Shubham Nilkanth Rahmatkar, Dinesh Yugraj Gawande, Milind Janraoji Umekar, Brijesh Gulabrao Taksande&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Pharmacology, Division of Neuroscience, Shrimati Kishoritai Bhoyar College of Pharmacy, New Kamptee, Nagpur (M.S.), INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Surapong Rattana</style></author><author><style face="normal" font="default" size="100%">Teeraporn Katisart</style></author><author><style face="normal" font="default" size="100%">Bunleu Sungthong</style></author><author><style face="normal" font="default" size="100%">Chirapha Butiman</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Acute and Sub-acute Toxicities of Thai Silkworm Powder (Bombyx mori Linn.) From Three Races in Male Wistar Rats and In vitro Antioxidant Activities</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antioxidant activities.</style></keyword><keyword><style  face="normal" font="default" size="100%">hematological parameters</style></keyword><keyword><style  face="normal" font="default" size="100%">lipid profile</style></keyword><keyword><style  face="normal" font="default" size="100%">Silkworm</style></keyword><keyword><style  face="normal" font="default" size="100%">toxicities</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-4/10.5530pj.2017.4.87</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">541-545</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; The silkworm powder from Japanese and Korean races has a high biological activity. However, there was less scientific evidence regarding bioactivities in Thai silkworm races. &lt;strong&gt;Objective:&lt;/strong&gt; This research was interested in toxicity and antioxidant activities of Thai silkworm races. &lt;strong&gt;Material and methods:&lt;/strong&gt; The 5th instar, 3rd day of growth stage of Thai traditional silkworm (Nanglai, Nangnoi and Samrong races) were lyophilized by freeze dryer and ground as silkworm powder. The acute and sub-acute toxicities studies were carried out in male Wistar rats. The antioxidant capacities of silkworm powder were investigated with DPPH, ABTS and FRAP methods. &lt;strong&gt;Results:&lt;/strong&gt; The acute toxicity in rats by single dose oral administration show that the high dose at a concentration of 2,000 mg/kg b.w. did not have toxicity in rats. The sub-acute toxicity in rats by oral administration showed that the high dose concentration at 2,000 mg/kg body weight for 6 weeks had no toxicity in all group either. In addition, the hematological parameters and lipid profiles of treated group and control groups were not significantly different. The antioxidant study showed that silkworm powders were not significant difference in all groups of samples in three assays (DPPH, ABTS and FRAP). However, significant difference had been found in comparison to ascorbic acid (p &amp;lt; 0.05). &lt;strong&gt;Conclusion:&lt;/strong&gt; Silkworm powder from three races of Thai silkworm did not produce any toxicity in male rats. In addition, the silkworm powder also exhibited antioxidant activities.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">541</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Surapong Rattana&lt;sup&gt;1&lt;/sup&gt;*, Teeraporn Katisart&lt;sup&gt;2&lt;/sup&gt;, Bunleu Sungthong&lt;sup&gt;3&lt;/sup&gt;, Chirapha Butiman&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biology, Faculty of Science, Mahasarakham University, Maha Sarakham, 44150, THAILAND.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biology, Faculty of Science, Mahasarakham University, Maha Sarakham, 44150, THAILAND.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Pharmaceutical Chemistry and Natural Products Research Unit, Faculty of Pharmacy, Mahasarakham University, Maha Sarakham, 44150, THAILAND.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Silk Innovation Center, Mahasarakham University, Maha Sarakham, 44150, THAILAND.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Berna Elya</style></author><author><style face="normal" font="default" size="100%">Basah Katrin</style></author><author><style face="normal" font="default" size="100%">Roshamur Cahyan Forestrania</style></author><author><style face="normal" font="default" size="100%">Rosmalena Sofyan</style></author><author><style face="normal" font="default" size="100%">Ryan Adi Chandra</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Alkaloid from Phoebe declinata Nees Leaves</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alkaloid</style></keyword><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">MCF-7 cell line.</style></keyword><keyword><style  face="normal" font="default" size="100%">Phoebe declinata nees</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/165</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">713-720</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Genus Phoebe have been reported to produce isoquinoline alkaloids as aporphines, noraporphines, and benzylisoquinolines. Many of these isolates exhibit diversified biological activities, including cytotoxic activity. &lt;strong&gt;Objective:&lt;/strong&gt; The objective of this study is to determine cytotoxic activity of compound isolated from &lt;em&gt;Phoebe declinata&lt;/em&gt; againts MCF-7 (breast cancer cell line). &lt;strong&gt;Methods:&lt;/strong&gt; Extraction was done by reflux using n-hexane, antioxidant activity measured by DPPH method and reducing power method, cytotoxic activity measured by MTT assay using MCF-7 cell line, struture eucidation was confirmed by NMR. &lt;strong&gt;Results:&lt;/strong&gt; The antioxidant activity measured using DPPH method for 1 and 2 showed IC&lt;sub&gt;50&lt;/sub&gt; value of 6.42 and 11.80 &amp;mu;g/mL respectively and using reducing power method for 1 and 2 showed IC&lt;sub&gt;50&lt;/sub&gt; value of 7.02 and 13.74 &amp;mu;g/mL respectively. Compound (1) and (2) exhibited cytotoxic activity against MCF-7 cells with an IC&lt;sub&gt;50&lt;/sub&gt; value of 82.978 and 93.179 &amp;mu;g/mL. &lt;strong&gt;Conclusion:&lt;/strong&gt; Compound (1) and (2) exhibited antioxidant activity and cytotoxic activity against MCF-7.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">713</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Berna Elya&lt;sup&gt;1,2*&lt;/sup&gt;, Basah Katrin&lt;sup&gt;1&lt;/sup&gt;, Roshamur Cahyan Forestrania&lt;sup&gt;1&lt;/sup&gt;, Rosmalena Sofyan&lt;sup&gt;3,&amp;nbsp;&lt;/sup&gt;Ryan Adi Chandra&lt;sup&gt;3&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Faculty of Pharmacy, University of Indonesia, Kampus UI Depok,16424.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Center of Study on Natural Products, University of Indonesia, Kampus UI Depok,16424.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Medicine, University of Indonesia, Kampus UI depok, 16424.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Toru Konishi</style></author><author><style face="normal" font="default" size="100%">Masaaki Minami</style></author><author><style face="normal" font="default" size="100%">Toshiaki Makino</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antibacterial Activity Of Shin’iseihaito (Xinyiqingfeitang) And its Components Against Methicillin-Resistant Staphylococcus aureus</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Methicillin-resistant Staphylococcus aureus (MRSA)</style></keyword><keyword><style  face="normal" font="default" size="100%">Scutellaria baicalensis</style></keyword><keyword><style  face="normal" font="default" size="100%">Shin’iseihaito</style></keyword><keyword><style  face="normal" font="default" size="100%">Sinusitis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2017 </style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-3/10.5530pj.2017.3.53</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">310-314</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; Shin&amp;rsquo;iseihaito (xinyiqingfeitang in Chinese, SSHT), a formula in traditional Japanese Kampo medicine and Chinese medicine comprising nine crude drugs, Gypsum, Ophiopogon Tuber, Scutellaria Root (SR, root of &lt;em&gt;Scutellaria baicalensis&lt;/em&gt;), Gardenia Fruit, Anemarrhena Rhizome, Lilium Bulb, Magnolia Flower, Loquat Leaf, and Cimicifuga Rhizome (CR, rhizome of &lt;em&gt;Cimicifuga heracleifolia&lt;/em&gt;), is commonly used to treat sinusitis associated with purulent nasal discharge and reddish nasal mucosa. We evaluated anti-bacterial activity of SSHT extract on methicillin-resistant &lt;em&gt;Staphylococcus aureus&lt;/em&gt; (MRSA), one cause of bacterial sinusitis. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Sterile paper disks impregnated with SSHT extract, the combination of crude drugs composing SSHT according to the traditional pharmacological theory, or each component were placed on Mueller-Hinton agar plates inoculated with several strains of MRSA isolated from the patients. The diameter of inhibitory zone was measured after 18&amp;ndash;24 h incubation. &lt;strong&gt;Results:&lt;/strong&gt; SSHT extract showed antibacterial activity against 128/190 (66.8%) MRSA clinical isolates. The effect of the extract of SSHT without heat-clearing drugs (SSHT&amp;ndash;HC) or without exterior-releasing drugs (SSHT&amp;ndash;ER) were significantly lower than that of SSHT extract. Each water extract of SR, Loquat Leaf, Magnolia Flower and CR showed significant anti-MRSA activity, and SR extract exhibited the largest inhibitory zone. &lt;strong&gt;Conclusions:&lt;/strong&gt; SSHT has antibacterial activity against MRSA clinical isolates, and SR mainly contributes to the antibacterial activity of SSHT against MRSA clinical isolates.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">310</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Toru Konishi&lt;sup&gt;1&lt;/sup&gt;, Masaaki Minami&lt;sup&gt;2&lt;/sup&gt;, Toshiaki Makino&lt;sup&gt;1* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-dori, Mizuho-ku, Nagoya 467-8603, JAPAN.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Bacteriology, Graduate School of Medical Sciences, Nagoya City University,1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, JAPAN.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arif Budiman</style></author><author><style face="normal" font="default" size="100%">Diah Lia Aulifa</style></author><author><style face="normal" font="default" size="100%">Arif Satria Wira Kusuma</style></author><author><style face="normal" font="default" size="100%">Astri Sulastri</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antibacterial and Antioxidant Activity of Black Mulberry (Morus nigra L.) Extract for Acne Treatment</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti acne</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Morus Nigra Extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Propionibacterium Acnes</style></keyword><keyword><style  face="normal" font="default" size="100%">Staphylococcus Epidermidis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/pj-9-5/10.5530pj.2017.5.97/index.html</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">611-614</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Black mulberry is rich in phenols and is hence usable in the treatment of acne. It also contains anthocyanin, a well-known antioxidant. This study aimed to examine the antibacterial and antioxidant properties of black mulberry (&lt;em&gt;Morus nigra L.&lt;/em&gt;) extract as a potential raw material for use in beauty care products. &lt;strong&gt;Method: &lt;/strong&gt;Fruit extract was obtained using maceration method with 96% ethanol. The antibacterial activity of the extract was determined by disc diffusion method, while the minimal inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were determined by microdilution method. Furthermore, the antioxidant activity of the extract was tested by DPPH method. &lt;strong&gt;Result:&lt;/strong&gt; The results showed a 2.5% MIC against &lt;em&gt;S. epidermidis&lt;/em&gt; and &lt;em&gt;P. acnes,&lt;/em&gt; confirming the antibacterial activity of black mulberry extract. The MBC values for the respective bacterium were 2.5% and 5%. Regarding antioxidant activity, the IC&lt;sub&gt;50&lt;/sub&gt; value of black mulberry extract was 146.731 mg/mL, suggesting its medium potential. &lt;strong&gt;Conclusion:&lt;/strong&gt; &lt;em&gt;Morus nigra&lt;/em&gt; extract has antibacterial activity against &lt;em&gt;S. epidermidis &lt;/em&gt;and &lt;em&gt;P. acnes&lt;/em&gt;, and has medium potential as antioxidant.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">611</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Arif Budiman&lt;sup&gt;1*&lt;/sup&gt;, Diah Lia Aulifa&lt;sup&gt;2&lt;/sup&gt;, Arif Satria Wira Kusuma&lt;sup&gt;1&lt;/sup&gt;, Astri Sulastri&lt;sup&gt;1 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Departement of Pharmaceutical and Technology Pharmacy, Universitas Padjadjaran Jatinangor, INDONESIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Sekolah Tinggi Farmasi Indonesia, Jl. Soekarno Hatta No. 354, Bandung, INDONESIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Surapong Rattana</style></author><author><style face="normal" font="default" size="100%">Teeraporn Katisart</style></author><author><style face="normal" font="default" size="100%">Chirapha Butiman</style></author><author><style face="normal" font="default" size="100%">Bunleu Sungthong</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antihyperglycemic Effect of Silkworm Powder, Fibroin and Sericin from Three Thai Silkworm (Bombyx mori Linn.) in Streptozotocin-Induced Diabetic Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antihyperglycemic effect</style></keyword><keyword><style  face="normal" font="default" size="100%">Diabetic rats</style></keyword><keyword><style  face="normal" font="default" size="100%">Fibroin.</style></keyword><keyword><style  face="normal" font="default" size="100%">Sericin</style></keyword><keyword><style  face="normal" font="default" size="100%">Silkworm</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-4/10.5530pj.2017.4.89</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">559-564</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; The present study was aimed to investigate the antihyperglycemic activities of Thai silkworm (&lt;em&gt;Bombyx mori &lt;/em&gt;Linn.) powder, fibroin and sericin from three races of Thai silkworm including Nangnoi, Nanglai, and Samrong in streptozotocin-induced diabetic rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; All rats were daily and orally administered with silkworm powder (5&lt;sup&gt;th&lt;/sup&gt;-instar, 3&lt;sup&gt;rd&lt;/sup&gt;-day), fibroin, and sericin at a dose of 250 mg/kg for 6 weeks. After that, various parameters including body weight, blood glucose, hematological and biochemical parameters were determined. &lt;strong&gt;Results:&lt;/strong&gt; The results revealed that fasting plasma glucose level in 6&lt;sup&gt;th&lt;/sup&gt; week of Nanglai fibroin, Nangnoi fibroin and Nangnoi sericin expressed a better reduction of FPG in diabetic rats compared with diabetic control groups (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05). All hematological parameters of each group were not different within those values (&lt;em&gt;p&lt;/em&gt;&amp;gt;0.05). In case of blood urea nitrogen, creatinine and alkaline phosphatase value showed that some of treated groups was different from diabetic control (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05), while all of treated groups showed different in cholesterol and high density lipoprotein value (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05). &lt;strong&gt;Conclusion:&lt;/strong&gt; Silkworm powders, fibroin and sericin of three races exhibited a therapeutic potential for the reduction plasma glucose level. Treatments of silkworm powder, fibroin and sericin did not have any effect on hematological parameters. Improvement of blood urea nitrogen, creatinine, alkaline phosphatase values and lipid profiles also were also observed in the treatment groups.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">559</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Surapong Rattana&lt;sup&gt;1*&lt;/sup&gt;, Teeraporn Katisart&lt;sup&gt;2&lt;/sup&gt;, Chirapha Butiman&lt;sup&gt;3&lt;/sup&gt;, Bunleu Sungthong&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;em&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biology, Faculty of Science, Mahasarakham University, Maha Sarakham, 44150, THAILAND. &lt;/em&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;em&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biology, Faculty of Science, Mahasarakham University, Maha Sarakham, 44150, THAILAND. &lt;/em&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;em&gt;&lt;sup&gt;3&lt;/sup&gt;Silk Innovation Center, Mahasarakham University, Maha Sarakham, 44150, THAILAND. &lt;/em&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;em&gt;&lt;sup&gt;4&lt;/sup&gt;Pharmaceutical Chemistry and Natural Products Research Unit, Faculty of Pharmacy, Mahasarakham University, Maha Sarakham, 44150, THAILAND.&lt;/em&gt;&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dinesh Murugan Girija</style></author><author><style face="normal" font="default" size="100%">Mangathayaru Kalachaveedu</style></author><author><style face="normal" font="default" size="100%">Rajasekaran Subbarayan</style></author><author><style face="normal" font="default" size="100%">Preethi Jenifer</style></author><author><style face="normal" font="default" size="100%">Suresh Ranga Rao</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Aristolochia bracteolata Enhances Wound Healing in vitro through Anti-inflammatory and Proliferative Effect on Human Dermal Fibroblasts and Keratinocytes</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">A. bracteolata</style></keyword><keyword><style  face="normal" font="default" size="100%">Fibroblast</style></keyword><keyword><style  face="normal" font="default" size="100%">Keratinocytes</style></keyword><keyword><style  face="normal" font="default" size="100%">RAW 264.7</style></keyword><keyword><style  face="normal" font="default" size="100%">Scratch assay</style></keyword><keyword><style  face="normal" font="default" size="100%">Wound Healing</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/394</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s129-s136</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; In the present study, we examined the effect of &lt;em&gt;Aristolochia bracteolata&lt;/em&gt; extract on Human dermal fibroblast (HDF) and Human keratinocyte cell line (HaCaT) proliferation and migration during&lt;em&gt; in vitro&lt;/em&gt; wound healing and its underlying mechanism. &lt;strong&gt;Method:&lt;/strong&gt; &lt;em&gt;A. bracteolata&lt;/em&gt; was collected and extracted using methanol. Cytotoxiciy effect of plant extract was determined by MTT assay in HDF and HaCaT. &lt;em&gt;In vitro&lt;/em&gt; Scratch assay determined the effect of plant extracts on migration of cells and its underlying mechanism was determined by RT-PCR analysis. &lt;strong&gt;Result:&lt;/strong&gt; The plant extract of &lt;em&gt;A. bracteolata&lt;/em&gt; selectively inhibited proliferation of both the cells at higher concentration (&amp;gt;100 &amp;mu;g/mL) and at lower concentrations (&amp;lt;25 &amp;mu;g/mL), it exhibited linear and dose-dependent cell proliferation. IC&lt;sub&gt;50&lt;/sub&gt; value was 87.60&amp;plusmn;1.67 &amp;mu;g/mL for HDF and 85.50&amp;plusmn;1.65 &amp;mu;g/mL after 24 h treatment. &lt;em&gt;In vitro&lt;/em&gt; scratch wound healing studies showed wound closure of 50.38%&amp;plusmn;1.39 and 69.81%&amp;plusmn;1.89 at a concentration of 25 &amp;mu;g/mL after 24 h and 48 h, respectively. The extract was tested for anti-inflammatory activity by determination of inhibitory activity on lipopolysaccharide (LPS) induced nitric oxide (NO) production in RAW 264.7 cell lines. We found that &lt;em&gt;A. bracteolata&lt;/em&gt; has a strong inhibitory effect on the production of NO and tumor necrosis factor-&amp;alpha; (TNF-&amp;alpha;). The plant extract of &lt;em&gt;A. bracteolata&lt;/em&gt; inhibited inducible nitric oxide synthase (iNOS) gene expression by lipopolysaccharide (LPS). To explore the mechanism responsible for the inhibition of iNOS, gene expression was analyzed by Real- Time PCR. &lt;em&gt;A. bracteolata&lt;/em&gt; showed a decrease in the expression of pro-inflammatory cytokine mRNA in a concentration-dependent manner. Treatment with the plant extract resulted in enhanced expression of Collagen 1 a (I) and Collagen IV in HDFs by regulating the mRNA levels of extracellular matrix (ECM) proteins and Matrix metalloproteinase-2. &lt;strong&gt;Conclusion:&lt;/strong&gt; Thus, the present investigation scientifically validates the use of &lt;em&gt;A. bracteolata &lt;/em&gt;in wound healing.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s129</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Dinesh Murugan Girija&lt;sup&gt;1&lt;/sup&gt;, Mangathayaru Kalachaveedu&lt;sup&gt;2&lt;/sup&gt;*, Rajasekaran Subbarayan&lt;sup&gt;3&lt;/sup&gt;, Preethi Jenifer&lt;sup&gt;2&lt;/sup&gt;, Suresh Ranga Rao&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Centre for Indian Systems of Medicine Quality Assurance and Standardization Sri Ramachandra University, Chennai, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Pharmacy, Sri Ramachandra University, Chennai, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Centre for Regenerative Medicine and Stem Cell Research, Sri Ramachandra University, Chennai, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Periodontology, Sri Ramachandra University, Chennai, Tamil Nadu, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ajay Pal</style></author><author><style face="normal" font="default" size="100%">Kandikattu Hemanth Kumar</style></author><author><style face="normal" font="default" size="100%">Bharat Bhushan</style></author><author><style face="normal" font="default" size="100%">Vinod Saharan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ashwagandha Root Extract Inhibits Acetylcholine Esterase, Protein Modification and Ameliorates H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;-Induced Oxidative Stress in Rat Lymphocytes</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acetylcholine esterase</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidants</style></keyword><keyword><style  face="normal" font="default" size="100%">Ashwagandha</style></keyword><keyword><style  face="normal" font="default" size="100%">DNA damage</style></keyword><keyword><style  face="normal" font="default" size="100%">Protein carbonylation</style></keyword><keyword><style  face="normal" font="default" size="100%">Rat lymphocytes</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2017 </style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-3/10.5530pj.2017.3.52</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">302-309</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Herbs have long been the basis of medical treatment but the practice of herbalism is not strictly based on evidences gathered using scientific methods. Ashwagandha (&lt;em&gt;Withania somnifera L&lt;/em&gt;.) is a traditional medicinal herb used in the treatment of various ailments. &lt;strong&gt;Objective:&lt;/strong&gt; In current study we have evaluated the acetylcholine esterase (AChE) inhibitory and antioxidant potential of Ashwagandha root extract (ARE) in in-vitro and &lt;em&gt;ex-vivo&lt;/em&gt; models to give a scientific base to its use in herbal medicine. &lt;strong&gt;Methodology:&lt;/strong&gt; Simplest extraction e.g. maceration method was performed for preparation of extracts using methanol as solvent. Both &lt;em&gt;in vitro&lt;/em&gt; and &lt;em&gt;in vivo&lt;/em&gt; experimental trial were executed to evaluate the efficacy of root extract. &lt;strong&gt;Result and Discussion:&lt;/strong&gt; ARE substantially scavenged free radicals and effectively prevented protein degradation as well as modification as studied by SDS-PAGE and Western blotting. Pre-treatment with ARE protected rat lymphocytes against H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;-induced oxidative damage. H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; treatment resulted in DNA fragmentation and significantly decreased the activities of key antioxidant enzymes namely superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase, glucose-6-phosphate dehydrogenase while decreased and increased the content of glutathione and malondialdehyde, respectively. ARE pre-treatment almost reversed these changes indicating its efficiency to suppress hydrogen peroxide-induced oxidative stress. &lt;strong&gt;Conclusion:&lt;/strong&gt; The study provides the scientific basis of pleiotropic functions of Ashwagandha.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">302</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ajay Pal&lt;sup&gt;1&lt;/sup&gt;, Kandikattu Hemanth Kumar&lt;sup&gt;2&lt;/sup&gt;, Bharat Bhushan&lt;sup&gt;*1&lt;/sup&gt; and Vinod Saharan&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry and Biochemistry, Chaudhary Charan Singh Haryana Agricultural University, Hisar, Haryana, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Biochemistry and Nanosciences Discipline, Defence Food Research Laboratory, Mysore, Karnataka, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Molecular Biology and Biotechnology, Maharana Pratap University of Agriculture and Technology, Udaipur, Rajasthan, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sivadasan Deepa</style></author><author><style face="normal" font="default" size="100%">Pitchiah Venkateshwaran</style></author><author><style face="normal" font="default" size="100%">Nambali Valsalan Vinithkumar</style></author><author><style face="normal" font="default" size="100%">Ramalingam Kirubagaran</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bioactive Propensity of Macroalgae from the Andaman &amp; Nicobar Islands</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibiofilm</style></keyword><keyword><style  face="normal" font="default" size="100%">Antifouling</style></keyword><keyword><style  face="normal" font="default" size="100%">Antimicrobial</style></keyword><keyword><style  face="normal" font="default" size="100%">Bioactivity</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxic Effect</style></keyword><keyword><style  face="normal" font="default" size="100%">Marine Macro Algae.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/180</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">815-820</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aims:&lt;/strong&gt; Marine macroalgae are the rich source of biologically active metabolites and potential source for development of novel biotechnological products. The present study was made to explore the metabolically active compounds from the macroalgae of the Andaman &amp;amp; Nicobar Islands. Methods and &lt;strong&gt;Material:&lt;/strong&gt; Different solvents such as methanol (MeOH), ethyl acetate (EtoAc), butanol (BuOH) and aqueous (H&lt;sub&gt;2&lt;/sub&gt;O) extracts of nine macroalgae were tested for antimicrobial, antibiofilm and cytotoxicity (brine shrimp larvae).&lt;strong&gt; Results:&lt;/strong&gt; Out of the 36 extracts 27 extracts showed antimicrobial activity against the human pathogens and 14 extracts revealed antibiofilm activities. The three EtoAc extracts of &lt;em&gt;Sargassum ilicifolium&lt;/em&gt;, MeOH extract of Sargassum sp. and MeOH extract of &lt;em&gt;Padina tetrastromatica&lt;/em&gt; showed inhibition against 8 pathogenic bacteria. Also, aqueous extract of &lt;em&gt;Padina tetrastromatica&lt;/em&gt; (71.82 %) and BuOH extract of &lt;em&gt;Dictyosphaeria cavernosa&lt;/em&gt; (71.58 %) exhibited higher antibiofilm nature. The highest cytotoxic effect was exhibited by species &lt;em&gt;Actinotrichia fragilis&lt;/em&gt; and all its four extracts significantly (P&amp;lt;0.01) inhibited the brine shrimp larvae, among this aqueous extract showed the lowest LC&lt;sub&gt;50&lt;/sub&gt; value, 31.7 &amp;mu;g/ml, followed by EtoAc extract, 89.33 &amp;mu;g/ml. &lt;strong&gt;Conclusion:&lt;/strong&gt; It was observed that different species have different kind of bioactive nature.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">815</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Sivadasan Deepa&lt;sup&gt;1*&lt;/sup&gt; Pitchiah Venkateshwaran&lt;sup&gt;1&lt;/sup&gt;, Nambali Valsalan Vinithkumar&lt;sup&gt;1&lt;/sup&gt;, Ramalingam Kirubagaran&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Andaman and Nicobar Centre for Ocean Science and Technology, Earth System Sciences Organizations- National Institute of Ocean Technology (ESSO-NIOT), Ministry of Earth Sciences, Government of India, Port Blair 744 103, Andaman &amp;amp; Nicobar Islands, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt; Earth System Sciences Organizations- National Institute of Ocean Technology (ESSO-NIOT), Ministry of Earth Sciences, Government of India, Chennai 600 100, Tamil Nadu, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Saffidine Karima</style></author><author><style face="normal" font="default" size="100%">Chirol Nadine</style></author><author><style face="normal" font="default" size="100%">Benayache Fadila</style></author><author><style face="normal" font="default" size="100%">Jay Maurice</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Characterization and Distribution of Flavonoids from Flowers in Different Horticultural Types of Begonia.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Begonia</style></keyword><keyword><style  face="normal" font="default" size="100%">Chemotype</style></keyword><keyword><style  face="normal" font="default" size="100%">Distribution</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/186</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">850-855</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; The &lt;em&gt;begonias&lt;/em&gt; are ornamental plants known by the varied forms and colors of their flowers, as well as their decorative foliage. &lt;strong&gt;Objective:&lt;/strong&gt; This study attempts to characterize the flavonoids isolated from flower extracts of different horticultural cultivars of the genus &lt;em&gt;Begonia&lt;/em&gt;. &lt;strong&gt;Material and methods:&lt;/strong&gt; The compounds of the ethyl acetate and aqueous extracts were separated by chromatographic methods and identified by UV spectra and chemical techniques. &lt;strong&gt;Results:&lt;/strong&gt; The analysis allowed the characterization of flavonoids belonging to flavonol types in the free aglycones and glycoside forms of kaempferol and quercetin. On the other hand, fingerprinting analysis and quantification of major flavonoids of 184 cultivars were performed by high-performance liquid chromatography (HPLC). Among twenty five (25) components which were detected and separated: ten were corresponding to quercetin 3-Oglucosyl- rhamnoside (Rt=23.5), quercetin 3-O-glucoside (Rt=25), kaempferol 3-O-glucosylrhamnoside and its acylated derivative (Rt=32), kaempferol 3-O-glucoside (Rt=33), quercetin 3-O-p.coumaroyl-diglucoside (Rt=37), quercetin 3-O-P.coumaroyl-glucoside (Rt=40.5), quercetin (Rt=41.5), kaempferol and its acylated derivative (Rt=47). Only non-acylated glycosides of quercetin and kaempferol contributed to chemical variations among different cultivars based on the results of PCA. &lt;strong&gt;Conclusion:&lt;/strong&gt; The genus &lt;em&gt;Begonia&lt;/em&gt; is very heterogeneous and it is possible to distinguish several chemotypes whose differences rely on the complementarities between the metabolic pathways involved in the biosynthesis of glycosides of quercetin and kaempferol.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">850</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Saffidine Karima&lt;sup&gt;1*&lt;/sup&gt;, Chirol Nadine&lt;sup&gt;2&lt;/sup&gt;, Benayache Fadila&lt;sup&gt;3&lt;/sup&gt;, Jay Maurice&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Medicine, Faculty of Medicine, University Ferhat Abbas, S&amp;eacute;tif, ALGERIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Laboratory of Phytochemistry, University Claude Bernard-Lyon I, Villeurbanne, FRANCE.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;University Fr&amp;egrave;res Mentouri Constantine 1, Constantine, ALGERIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mahendra Shivshankar Khyade</style></author><author><style face="normal" font="default" size="100%">Mohan Baban Waman</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chemical Profile and Antioxidant Properties of Mundulea sericea</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS</style></keyword><keyword><style  face="normal" font="default" size="100%">Leaf extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Mundulea sericea</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolics</style></keyword><keyword><style  face="normal" font="default" size="100%">RP-HPLC</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">February 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://phcogj.com/fulltext/303</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">213-220</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objectives:&lt;/strong&gt; To evaluate the phytochemical composition and the antioxidant activity of aqueous-methanolic (20:80) leaves extract of &lt;em&gt;Mundulea sericea&lt;/em&gt; Willd. &lt;strong&gt;Methods:&lt;/strong&gt; The extract of leaves was tested for antioxidant activity using various &lt;em&gt;in vitro&lt;/em&gt; models viz., 2,2-diphenyl-1-picrylhydrazyl (DPPH), nitric oxide, ABTS, ferric reducing antioxidant power (FRAP), total antioxidant activity and reducing power. The phytochemical composition (GC-MS and HPLC) along with total phenolic and flavonoid content of the extract at different concentrations were also determined. &lt;strong&gt;Results:&lt;/strong&gt; Total phenolic and flavonoid contents were found to be equivalents to 107.86 &amp;plusmn; 0.53 &lt;em&gt;&amp;mu;&lt;/em&gt;g of gallic acid and 44.53 &amp;plusmn; 0.156 &lt;em&gt;&amp;mu;&lt;/em&gt;g of rutin /mg of dried hydro-methanolic methanolic extract, respectively. Among various antioxidant assays performed, maximum inhibition was observed for ABTS (IC&lt;sub&gt;50&lt;/sub&gt; 13.26 &amp;plusmn; 0.396 &lt;em&gt;&amp;mu;&lt;/em&gt;g) followed by DPPH (IC&lt;sub&gt;50&lt;/sub&gt; 79.83 &amp;plusmn; 0.306 &lt;em&gt;&amp;mu;&lt;/em&gt;g) and NO (IC&lt;sub&gt;50&lt;/sub&gt; 6.35 &amp;plusmn; 0.23 &lt;em&gt;&amp;mu;&lt;/em&gt;g/mL) assay. The GC-MS analysis revealed over 38 compounds; the prevailing compounds were Sec- Butyl ethyl sulfoxide and Di-methyl sulfoxonium formyl methylide. The RP-HPLC analysis further confirmed the presence of rutin, cinnamic acid and salicylic acid. &lt;strong&gt;Conclusion:&lt;/strong&gt; The results of the present study demonstrated that &lt;em&gt;Mundulea sericea&lt;/em&gt; leaves possess high phenolic with flavonoid contents and also revealed potential antioxidant activity so these leaves could be used as a viable source of natural antioxidants for industrial and pharmaceutical preparations.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">213</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Mahendra Shivshankar Khyade*&lt;sup&gt;1&lt;/sup&gt;, Mohan Baban Waman&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Botany, S.N. Arts, D.J.M. Commerce and B.N.S. Science College, Sangamner- 422605.Affiliated to Savitribai Phule Pune University, Pune (MS), INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Dr. D.Y. Patil Arts, Commerce and Science College, Pune- 411044, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Areeya Suchantabud</style></author><author><style face="normal" font="default" size="100%">Teeraporn Katisart</style></author><author><style face="normal" font="default" size="100%">Chusri Talubmook</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chronic Toxicity of Leaf Extract from Sphagneticola trilobata (L.) Pruski</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Blood biochemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">Chronic toxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Hematological values</style></keyword><keyword><style  face="normal" font="default" size="100%">Histological feature</style></keyword><keyword><style  face="normal" font="default" size="100%">S. trilobata</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2017 </style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-3/10.5530pj.2017.3.55</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">323-328</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Context:&lt;/strong&gt; &lt;em&gt;Sphagneticola trilobata&lt;/em&gt; (L.) Pruski. is a member of the family Asteraceae and has used traditionally in the prevention and treatment of various diseases. &lt;strong&gt;Aim:&lt;/strong&gt; The research was aimed to determine chronic toxicity of 80% ethanolic leaf extract from &lt;em&gt;S.trilobata&lt;/em&gt; (STLE). Materials and Methods: STLE at the doses of 200 or 400 mg/kg b. w. was oral given to the healthy Wistar rats daily for 90 days. &lt;strong&gt;Statistical analysis used:&lt;/strong&gt; Statistical analysis was carried out using F-test (One-Way ANOVA) followed by Duncan&amp;rsquo;s New Multiple Range Test. &lt;strong&gt;Results:&lt;/strong&gt; STLE did not produce any signs or symptoms of chronic toxicity. And also, the mortal rat was not observed during a period of an observation. Furthermore, STLE did not alter the body weight, relative organ (liver, pancreas, kidney and heart) weight, hemoglobin (Hb), hematocrit (Hct), red blood cell (RBC), white blood cell (WBC), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), neutrophil, lymphocyte, monocyte, platelet, alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), blood urea nitrogen (BUN), creatinine, blood cell characteristics, ultrastructure of RBC, and histological features of hepatic, pancreatic and renal tissues in the STLE treated rats comparing to control rats. &lt;strong&gt;Conclusions:&lt;/strong&gt; These findings indicate that the leaf extract from &lt;em&gt;S. trilobata&lt;/em&gt; exerts non chronic toxicity in rats and can be used safely as a traditional medicine or diet complement without any effect on hepatic and renal functions. &lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">323</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Areeya Suchantabud&lt;sup&gt;1*&lt;/sup&gt;, Teeraporn Katisart&lt;sup&gt;2&lt;/sup&gt;, Chusri Talubmook&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Candidate, Faculty of Science, Mahasarakham University, Kantarawichai, Maha Sarakham, 44150, THAILAND.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Science, Mahasarakham University, Kantarawichai, Maha Sarakham,44150, THAILAND.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Suresh Kumar Karri</style></author><author><style face="normal" font="default" size="100%">Angappan Sheela</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative in vitro Antidiabetic and Immunomodulatory Evaluation of Standardized Five Select Medicinal Herbs and Spectral Analysis of Boerhavia erecta L. (Nyctaginaceae)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">NBT assay</style></keyword><keyword><style  face="normal" font="default" size="100%">Nitric oxide</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognostic</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical</style></keyword><keyword><style  face="normal" font="default" size="100%">Quality control</style></keyword><keyword><style  face="normal" font="default" size="100%">TNF -α</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2017 </style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-3/10.5530pj.2017.3.57</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">336-344</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aim:&lt;/strong&gt; The present work compares standardized hydro-alcoholic extracts of root and stem parts of &lt;em&gt;Boerhavia erecta L.&lt;/em&gt; (&lt;em&gt;Nyctaginaceae&lt;/em&gt;), l&lt;em&gt;eaves of Plumeria acuminate&lt;/em&gt; R. Br. (Apocyanaceae), rhizomes of &lt;em&gt;Alpinia galanga&lt;/em&gt; Sw. (&lt;em&gt;Zingiberaceae&lt;/em&gt;), whole plant of &lt;em&gt;Picrorhiza kurroa&lt;/em&gt; Royle ex Benth. (Plantaginaceae), fruits of Trapa natans L. (Trapaceae) for their &lt;em&gt;in vitro&lt;/em&gt; antidiabetic and immunomodulatory activities, commonly used by the Trichigadi tribes (Kotas) of south India for various inflammatory disorders. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Antidiabetic activity of these herbal extracts was assessed through inhibition of glycosylation of hemoglobin and glucose uptake in yeast cells methods at 50, 100 and 200 &amp;mu;g/mL for 72 h. Their respective immunomodulatory activities were evaluated through preservation of heat and hypotonic induced hemolysis, nitroblue terazolium assay and by inhibition of TNF-&amp;alpha; and nitric oxide (NO) production in RAW cell lines. &lt;strong&gt;Results:&lt;/strong&gt; B. erecta has shown least cytotoxicity (CTC&lt;sub&gt;50&lt;/sub&gt; 15.7%) and highest % inhibition of TNF-&amp;alpha; (58.1) and NO (45.6), statistically significant (p&amp;lt;0.01) to that of normal control. Also, B. erecta (BE), and P. acuminate (PA) exhibited relatively better IC50 values for TNF-&amp;alpha; and NO at a concentration less than their respective CTC&lt;sub&gt;50&lt;/sub&gt; values. &lt;strong&gt;Conclusions&lt;/strong&gt;: Spectral analysis of chloroform fraction of BE hydro-alcoholic extract established the presence of biologically active molecule in it. Root and stem parts of BE extract not only proved to be safe but also demonstrated relatively better efficacy than other established medicinal herbs in selected immune models, may be due to flavonoids or phenolic groups. Further &lt;em&gt;in vivo&lt;/em&gt; studies on active molecule of BE towards antidiabetic and immunomodulatory activity are warranted.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">336</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Suresh Kumar Karri, Angappan Sheela* &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Chemistry, School of Advanced Sciences, VIT University, Vellore 632014, Tamil Nadu, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bosco Lawarence</style></author><author><style face="normal" font="default" size="100%">Murugan K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comprehensive Evaluation of Antioxidant Potential of Selected Osbeckia species and their in vitro Culture, Purification and Fractionation</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anthocyanins</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant Capacity</style></keyword><keyword><style  face="normal" font="default" size="100%">Free Radicals</style></keyword><keyword><style  face="normal" font="default" size="100%">Osbeckia Spp.</style></keyword><keyword><style  face="normal" font="default" size="100%">Reactive Oxygen Species</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/pj-9-5/10.5530pj.2017.5.107/index.html</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">674-682</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Health-benefit properties of natural pigments have been intensely studied, especially the anthocyanins. In the last few decades, research on anthocyanins has attracted biologists by the increasing evidence of their health beneficial effects. &lt;em&gt;Osbeckia,&lt;/em&gt; belongs to Melastomataceae and is well-known for colouring pigments and other bioactive compounds. In the present study, total anthocyanin and antioxidant capacity indicators were evaluated from 8 &lt;em&gt;Osbeckia&lt;/em&gt; spp. and anthocyanin was extracted from &lt;em&gt;in vitro&lt;/em&gt; cultures of &lt;em&gt;O. aspera&lt;/em&gt; and &lt;em&gt;O. reticulata&lt;/em&gt;. Materials and &lt;strong&gt;Methods:&lt;/strong&gt; The antioxidant effect was studied using ABTS (2, 2&amp;rsquo;-azino-bis-3-ethyl benzthiazoline-6-sulphonic acid) radical cation decolourisation assay, the FRAP, the scavenging ability of hydroxyl radicals and the superoxide anion scavenging activity. Anthocyanin extracted from &lt;em&gt;in vitro&lt;/em&gt; cultures were purified and fractionated using column chromatography and LC-MS MS analysis. &lt;strong&gt;Results:&lt;/strong&gt; &lt;em&gt;In vitro&lt;/em&gt; cultures of &lt;em&gt;O. aspera&lt;/em&gt; was obtained in MS medium fortified with various combinations of Benzyl Adenine (BA), Naphthalene acetic acid (NAA) and 2, 4-D. The chromatograms of &lt;em&gt;O. aspera&lt;/em&gt; revealed the presence of malvidin-3 -diglucoside, peonidin, delphinidin and cyanindin whereas &lt;em&gt;O. reticulata &lt;/em&gt;cultures accumulated large amounts of malvidin, cyanindin and cyanidin aglycone. The purified anthocyanins of these species were evaluated for their antioxidant potential and was found more remarkable than the crude extracts. &lt;strong&gt;Conclusion&lt;/strong&gt;: &lt;em&gt;Osbeckia&lt;/em&gt; species are rich in anthocyanin and therefore display potential AOX power. &lt;em&gt;O. aspera&lt;/em&gt; and &lt;em&gt;O. reticulata&lt;/em&gt; callus was induced &lt;em&gt;in vitro&lt;/em&gt; production of anthocyanins. The pool of anthocyanins was purified and fractionated by LCMS/ MS and AOX assays were performed with the purified anthocyanin which showed higher level activities.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">674</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Bosco Lawarence and Murugan K &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Plant Biochemistry and Molecular Biology Laboratory, University College, Trivandrum, Kerala, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gunjan Biswas</style></author><author><style face="normal" font="default" size="100%">Sudeshna Nandi</style></author><author><style face="normal" font="default" size="100%">Debashis Kuila</style></author><author><style face="normal" font="default" size="100%">Krishnendu Acharya</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Comprehensive Review on Food and Medicinal Prospects of Astraeus hygrometricus</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Astrakurkurone</style></keyword><keyword><style  face="normal" font="default" size="100%">Immunomodulation</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal Mushroom</style></keyword><keyword><style  face="normal" font="default" size="100%">Nutritive Value.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/178</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">799-806</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;Edible mushrooms contain unique flavours and textures. They have high nutritional and medicinal values and have been consumed worldwide. &lt;em&gt;Astraeus hygrometricus&lt;/em&gt; (Pers.) Morg. a wild ectomycorrhizal mushroom recognized as a food by the local people in South-East Asia as well as in Bihar, Jharkhand, South west India and South-Western region of West Bengal. However, it is considerably unknown to the communities in other parts of the world and it remains underutilized so far. Recent investigations from our laboratory have manifested the potential role of this mushroom in human health. Basidiocarps of &lt;em&gt;A. hygrometricus&lt;/em&gt; are rich in proteins, carbohydrates, minerals, crude fibre and essential amino acids with lower concentration of fat. Experiments on animal models reveal the hepatoprotective, cardioprotective, anti-inflammatory, anticancer and hypoglycaemic efficacy of the mushroom. Additionally, researchers have found this taxon to contain many bioactive compounds shown to be responsible for antitumor, anti-leishmanial, anticandidal, antioxidant and immunomodulatory activity. The present review, summarized the scattered literature on &lt;em&gt;A. hygrometricus&lt;/em&gt; with an emphasis on its nutritional and health promoting aspects.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">799</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Gunjan Biswas&lt;sup&gt;1*&lt;/sup&gt;, Sudeshna Nandi&lt;sup&gt;2*&lt;/sup&gt;, Debashis Kuila&lt;sup&gt;1&lt;/sup&gt;, Krishnendu Acharya&lt;sup&gt;2*&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Botany &amp;amp; Forestry, Vidyasagar University, Midnapore- 721102, West Bengal, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Molecular and Applied Mycology and Plant Pathology Laboratory, Department of Botany, University of Calcutta, 35, Ballygunge Circular Road, Kolkata, 700019, West Bengal, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rohin Mohd Adzim Khalili</style></author><author><style face="normal" font="default" size="100%">Jumli Mimie Noratiqah</style></author><author><style face="normal" font="default" size="100%">Ridzwan Norhaslinda</style></author><author><style face="normal" font="default" size="100%">Abd Hadi Norhayati</style></author><author><style face="normal" font="default" size="100%">Baig Atif Amin</style></author><author><style face="normal" font="default" size="100%">Arshad Roslan</style></author><author><style face="normal" font="default" size="100%">A. Latif Ahmad Zubaidi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cytotoxicity Effect and Morphological Study of Different Duku(Lansium domesticum corr.) Extract towards Human Colorectal Adenocarcinoma Cells Line (HT-29)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-proliferative effect</style></keyword><keyword><style  face="normal" font="default" size="100%">colorectal cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">IC50 value.</style></keyword><keyword><style  face="normal" font="default" size="100%">MTT Assay</style></keyword><keyword><style  face="normal" font="default" size="100%">polarity extracts</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/172</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">757-761</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Context:&lt;/strong&gt; &lt;em&gt;Lansium domesticum&lt;/em&gt; corr. is a member of the family Meliaceae, and known locally as duku and has been used traditionally in the prevention and treatment of various illness. &lt;strong&gt;Aim:&lt;/strong&gt; To study the cytotoxic effect and morphological changes of human colorectal adenocarcinoma cells (HT-29) treated with different duku &lt;em&gt;(Lansium domesticum&lt;/em&gt; corr.) extracts. &lt;strong&gt;Methods:&lt;/strong&gt; The &lt;em&gt;L.domesticum&lt;/em&gt; corr. fruit extracts were processed involving three different solvents; methanol, ethanol and ethyl acetate. HT-29 cell lines were treated with different concentrations of &lt;em&gt;L. domesticum&lt;/em&gt; corr. (0-100 &amp;mu;g/ml) extracts for a total of 24, 48 and 72 hours. Cytotoxicity of cells line was determined by using MTT assay as per IC&lt;sub&gt;50&lt;/sub&gt; values. &lt;strong&gt;Results:&lt;/strong&gt; Methanol extract of &lt;em&gt;L. domesticum&lt;/em&gt; corr. showed IC&lt;sub&gt;50&lt;/sub&gt; value at 6.79 &amp;plusmn; 0.00 &amp;mu;g/ml and 50.0 &amp;plusmn; 0.00 &amp;mu;g/ml respective, while ethyl acetate extract of L. domesticum corr. reached IC&lt;sub&gt;50&lt;/sub&gt; value at 86.00 &amp;plusmn; 0.08 &amp;mu;g/ml, and 96.0 &amp;plusmn; 0.12 &amp;mu;g/ml. There was no IC&lt;sub&gt;50&lt;/sub&gt; value of ethanol extract from &lt;em&gt;L.domesticum&lt;/em&gt; corr. Only methanol extract showed toxicity towards HT-29 cells line. &lt;strong&gt;Conclusion:&lt;/strong&gt; To the best of our knowledge, this is the first repeat the exploring the effect of duku (&lt;em&gt;L. domesticum&lt;/em&gt; corr.) extract on HT-29 cells line.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">757</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Rohin Mohd Adzim Khalili, Jumli Mimie Noratiqah, Ridzwan Norhaslinda, Abd Hadi Norhayati, Baig Atif Amin, Arshad Roslan, A. Latif Ahmad Zubaidi&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Faculty of Health Sciences, Universiti Sultan Zainal Abidin, Gong Badak Campus, Hafsah Block, 21300 Kuala Nerus, Terengganu Darul Iman, MALAYSIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mariam Koleilat</style></author><author><style face="normal" font="default" size="100%">Karim Raafat</style></author><author><style face="normal" font="default" size="100%">Abdalla El-Lakany</style></author><author><style face="normal" font="default" size="100%">Maha Aboul-Ela</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Designing monographs for Rosmarinus officinalis L. and Lavandula angustifolia L.: Two Lebanese species with significant medicinal potentials</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Glandular trichome</style></keyword><keyword><style  face="normal" font="default" size="100%">Optical rotation</style></keyword><keyword><style  face="normal" font="default" size="100%">Prismatic crystals of Calcium oxalate</style></keyword><keyword><style  face="normal" font="default" size="100%">Refractive index</style></keyword><keyword><style  face="normal" font="default" size="100%">Rosmarinic acid</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-4/10.5530pj.2017.4.75</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">452-474</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The world health organization recommends validating medicinal plants to ensure safety and efficacy. Lavandula is valued for the production of essential oil used in aromatherapy. &lt;em&gt;Rosmarinus &lt;/em&gt;is known for its folk use as anti-oxidant and antidiabetic. This study aims to design monographs for &lt;em&gt;Rosmarinus officinalis&lt;/em&gt; (Linn.) and &lt;em&gt;Lavandula angustifolia&lt;/em&gt; (Linn.) cultivated, in conditions similar to their natural habitat, at Beirut Arab University botanical garden. Also screening the antioxidant activity of both plants, and assessing the antidiabetic effect of &lt;em&gt;R. officinalis&lt;/em&gt; (Linn.). &lt;strong&gt;Methods:&lt;/strong&gt; macroscopic and microscopic examination, hydrodistillation to obtain essential oils (EOs), thin layer chromatography, Gas chromatography-Mass spectrometry, and physiochemical properties of the EOs were determined. The antioxidant effect of the EOs is determined by DPPH assay. The antidiabetic effect of Rosemary EO is investigated using alloxan-induced diabetic mice. &lt;strong&gt;Results:&lt;/strong&gt; the qualities of studied species are in agreement with the standards described in WHO monographs and in the British pharmacopeia. Composition of the EO produced from either Rosemary (REO) or Lavender (LEO) collected at different months showed differences. The EO of both showed significant antioxidant effects in DPPH assay (p&amp;lt;0.05). &lt;em&gt;In vivo&lt;/em&gt; investigation of the antidiabetic effect of REO showed a significant antidiabetic effect in diabetic mouse model (p&amp;lt;0.05). &lt;strong&gt;Conclusion:&lt;/strong&gt; both plant species and their EOs fulfilled most of standards specified by the British Pharmacopeia 2013. Rosemary collected in April (Spring) showed the best antioxidant activity. Lavender collected in September (Early Fall) showed the best antioxidant activity. REO revealed significant lowering in blood glucose level at the dose of 110 mg/kg.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">452</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Mariam Koleilat, Karim Raafat*, Abdalla El-Lakany, Maha Aboul- Ela &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Pharmaceutical Sciences, Faculty of Pharmacy, Beirut Arab University, 115020 Beirut, LEBANON.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Venkata Siva Satyanarayana Kantamreddi</style></author><author><style face="normal" font="default" size="100%">V. Thirumala Veni</style></author><author><style face="normal" font="default" size="100%">Murali Krishna Malasani</style></author><author><style face="normal" font="default" size="100%">Boddana Simhachalam</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Differentiation of Five Commercially Available Triphala churnas of an Ayurvedic Formulation by Elemental Fingerprint</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ayurvedic Drugs</style></keyword><keyword><style  face="normal" font="default" size="100%">Elemental Fingerprint</style></keyword><keyword><style  face="normal" font="default" size="100%">Fuzzy c-Means</style></keyword><keyword><style  face="normal" font="default" size="100%">Hierarchical Cluster Analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Inductively Coupled Plasma Mass Spectrometry</style></keyword><keyword><style  face="normal" font="default" size="100%">k-Means</style></keyword><keyword><style  face="normal" font="default" size="100%">Triphala churna</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">117-122.</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt;&lt;em&gt;Triphala churna&lt;/em&gt;&lt;/span&gt; (TPC) is one of the well known &lt;em&gt;Ayurvedic&lt;/em&gt; powdered preparations of Indian System of Medicine and is used in the treatment of various diseases. Elemental pattern of TPC was developed in order to investigate the identity and quality of commercial TPC drugs. &lt;strong&gt;Method:&lt;/strong&gt; Inductively coupled plasma mass spectrometry (ICP-MS) was used for the quantitative determination of ten essential and trace elements in five marketed samples of &lt;em&gt;Triphala churna&lt;/em&gt;. The concentration patterns of these elements were deciphered by multivariate statistical analysis such as hierarchical cluster analysis (HCA), fuzzy c-means (FCM) and k-means (KM) cluster analysis. &lt;strong&gt;Results:&lt;/strong&gt; The elemental concentrations ranged from 1.3 mg/kg (Cr, TPC3) to 14220 mg/kg (K, TPC4). The elemental fingerprint of &lt;em&gt;Triphala churna&lt;/em&gt; was established based on three churnas viz. TPC1, TPC3 and TPC5, which were found in one cluster with a very high degree of similarity by KM, FCM and HCA techniques. &lt;strong&gt;Conclusion:&lt;/strong&gt; Based on the results, the graphical pattern of elements detected in these samples can be considered as elemental fingerprint of &lt;em&gt;Triphala churna&lt;/em&gt; and can be used for authentication and/or to determine the quality of commercial TPC drugs.&amp;nbsp;&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">117</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Venkata Siva Satyanarayana Kantamreddi&lt;sup&gt;1&lt;/sup&gt;&lt;sup&gt;,2&lt;/sup&gt;*, Thirumala Veni Vasupalli&lt;sup&gt;1&lt;/sup&gt;, Murali Krishna Malasani&lt;sup&gt;2&lt;/sup&gt;, and Simhachalam Boddana&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Centre for Chemical Analysis, Central Research Laboratory, GIT, GITAM University, Visakhapatnam, INDIA&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;S.V. Enviro Labs &amp; Consultants, IDA, Auto Nagar, Visakhapatnam, INDIA&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Mathematics, GIT, GITAM University, Visakhapatnam, INDIA&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ankita Misra</style></author><author><style face="normal" font="default" size="100%">Akanksha Srivastava</style></author><author><style face="normal" font="default" size="100%">Mohammad Khalid</style></author><author><style face="normal" font="default" size="100%">Poonam Kushwaha</style></author><author><style face="normal" font="default" size="100%">Sharad Srivastava</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Anti Arthritic Potential of Gloriosa superba (L.) Elite Germplasm Collected from Eastern Himalayas, India</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti arthritic</style></keyword><keyword><style  face="normal" font="default" size="100%">Colchicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Elite chemotype</style></keyword><keyword><style  face="normal" font="default" size="100%">G. superba</style></keyword><keyword><style  face="normal" font="default" size="100%">HPTLC</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/387</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s87-s92</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Gloriosa superba&lt;/em&gt; (L.) is a traditionally known medicinal plant for its potential antigout property. The species is rich source of colchicine alkaloid and is commercially exploit in the international market for the same. &lt;strong&gt;Method:&lt;/strong&gt; In the present study, elite chemotype of &lt;em&gt;G. superba&lt;/em&gt; was identified from natural population in Eastern Himalayas based on their colchicine content through HPTLC calibrated method. The selected elite chemotypes were further evaluated for &lt;em&gt;in vitro&lt;/em&gt; anti-arthritic potential via inhibition of protein denaturation along with hydroxyl radical scavenging potential. &lt;strong&gt;Result:&lt;/strong&gt; The HPTLC quantification data reveals that the content of colchicine varies from 0.044 to 0.184% having maximum content in NBG-128 from Jorhat, Assam. The results of bioassay reflect a potentiating anti-arthritic and hydroxyl radical scavenging with statistically insignificant difference within the elite germplasms. &lt;strong&gt;Conclusion:&lt;/strong&gt; The presence of bioactive polyphenolics with significant hydroxyl radical scavenging will further suggest that inhibition of inflammatory mediator cells by extract is superimposed action of colchicine and other chemical inhibitors like polyphenolics. The study will aid in site specific exploration of high metabolite yielding chemotype(s) with validated pharmacological action for commercial cultivation to meet out the industrial demand of colchicine and herbal product development.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s87</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ankita Misra&lt;sup&gt;1,2,&lt;/sup&gt; Akanksha Srivastava&lt;sup&gt;1&lt;/sup&gt;, Mohammad Khalid&lt;sup&gt;2&lt;/sup&gt;, Poonam Kushwaha&lt;sup&gt;2&lt;/sup&gt;, Sharad Srivastava&lt;sup&gt;1&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Pharmacognosy and Ethnopharmacology Division, CSIR-National Botanical Research Institute, Lucknow, Uttar Pradesh 226001, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Pharmacy, Integral University, Lucknow, Uttar Pradesh 226001, INDIA.&amp;nbsp;&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Divneet Kaur</style></author><author><style face="normal" font="default" size="100%">Richa Shri</style></author><author><style face="normal" font="default" size="100%">Anjoo Kamboj</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Anti-Anxiety Effect of Brassica oleracea L. Extracts in Experimental Animals</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antianxiety</style></keyword><keyword><style  face="normal" font="default" size="100%">Brassica oleracea</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated Plus Maze</style></keyword><keyword><style  face="normal" font="default" size="100%">Hole Board</style></keyword><keyword><style  face="normal" font="default" size="100%">Mirror Chamber Test</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/pj-9-5/10.5530pj.2017.5.101/index.html</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">638-643</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Oxidative stress in the brain causes nervous system impairment. Hence the use of antioxidants could be an effective approach to prevent disorders such as anxiety. Plants containing phenolic constituents are reported to be potent antioxidants. &lt;em&gt;Brassica oleracea&lt;/em&gt; L. commonly known as broccoli, is rich in phenolics mainly flavonoids and possesses excellent antioxidant property, however its anxiolytic potential has not been investigated. Thus in the present study antianxiety activity of extracts of broccoli was evaluated in experimental animals. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Various pharmacognostic parameters of the plant material were studied following standard procedures. Groups of six mice each were taken as different treatment groups. Control group received vehicle (1% Carboxy Methyl Cellulose), positive control received Diazepam (2mg/kg) as standard drug while test groups received petroleum ether and hydroalcoholic extracts (50, 100 and 200 mg/kg body weight, p.o.). The effects were evaluated on Elevated Plus Maze (EPM), hole board and mirror chamber tests. Statistical analysis was performed using ANOVA, followed by Turkey&amp;rsquo;s post-hoc test. &lt;strong&gt;Results:&lt;/strong&gt; Hydroalcoholic extract shows dose dependent increase in the average time spent and frequency of entries in the open arms of the EPM; decreased latency, increased time spent and frequency of entries in the mirror chamber; increased number of head dips in hole board test as compared to control was observed. These effects were comparable to the effect produced by diazepam. Phytochemical screening of the bioactive extract revealed the presence of alkaloids, phenols, flavonoids and tannins. &lt;strong&gt;Conclusion:&lt;/strong&gt; From our study, it can be concluded that hydroalcoholic extract of &lt;em&gt;Brassica oleracea &lt;/em&gt;at the dose of 200 mg/kg possesses marked anxiolytic activity.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">638</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Divneet Kaur,&lt;sup&gt;1&lt;/sup&gt; Richa Shri,&lt;sup&gt;2&lt;/sup&gt; Anjoo Kamboj&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;I.K.Gujral Punjab Technical University, Jalandhar, INDIA&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Sciences and Drug Research, Patiala, INDIA&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Chandigarh College of Pharmacy, Landran, Mohali, Punjab, INDIA&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Krishnendu Acharya</style></author><author><style face="normal" font="default" size="100%">Kanad Das</style></author><author><style face="normal" font="default" size="100%">Soumitra Paloi</style></author><author><style face="normal" font="default" size="100%">Arun Kumar Dutta</style></author><author><style face="normal" font="default" size="100%">Manoj Emanuel Hembrom</style></author><author><style face="normal" font="default" size="100%">Somanjana Khatua</style></author><author><style face="normal" font="default" size="100%">Arvind Parihar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Exploring a novel edible mushroom Ramaria subalpina: Chemical characterization and Antioxidant activity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">Ferrous ion chelating</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC</style></keyword><keyword><style  face="normal" font="default" size="100%">India.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">30-34</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; During macrofungal inventorisation from an unexplored subalpine forest of Sikkim Himalayas, a new edible mushroom, &lt;em&gt;Ramaria subalpina&lt;/em&gt; was found and documented in consultation with the forest dwellers. &lt;strong&gt;Objective:&lt;/strong&gt; The aim of the present study was to understand the antioxidative potentiality and bioactive constituents of a novel taxon, &lt;em&gt;Ramaria subalpina&lt;/em&gt;, that is highly prized by the ethnic people of subalpine Sikkim Himalayas, India, for its flavor, texture and gastronomic delicacy since time immemorial. &lt;strong&gt;Methods:&lt;/strong&gt; Chemical composition and antioxidant properties of methanolic extract of dried basidiocarps were assessed using HPLC and several in vitro assay systems. &lt;strong&gt;Results:&lt;/strong&gt; Methanolic extract had phenolics in highest amount, among which pyrrogallol was identified. It also showed potent antioxidant activity. Conclusion: The present study suggests that &lt;em&gt;Ramaria subalpina&lt;/em&gt; has strong medicinal prospects. This novel mushroom can safely be added to the world&amp;rsquo;s edible mushrooms list.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">30</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Krishnendu Acharya&lt;sup&gt;1*&lt;/sup&gt;, Kanad Das&lt;sup&gt;2&lt;/sup&gt;, Soumitra Paloi&lt;sup&gt;1&lt;/sup&gt;, Arun Kumar Dutta&lt;sup&gt;1&lt;/sup&gt;, Manoj Emanuel Hembrom&lt;sup&gt;3&lt;/sup&gt;, Somanjana Khatua&lt;sup&gt;1&lt;/sup&gt;, and Arvind Parihar&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Botany, Molecular and Applied Mycology and Plant Pathology Laboratory, University of Calcutta, 35, Ballygunge Circular Road, Kolkata&amp;ndash;700019, West Bengal, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Cryptogamic Unit, Botanical Survey of India, P.O.&amp;ndash;Botanic Garden, Howrah&amp;ndash;711103, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Central National Herbarium, Botanical Survey of India, Central National Herbarium, P. O.&amp;ndash;Botanic Garden, Howrah &amp;ndash; 711103, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ampa Konsue</style></author><author><style face="normal" font="default" size="100%">Chayan Picheansoonthon</style></author><author><style face="normal" font="default" size="100%">Chusri Talubmook</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fasting Blood Glucose Levels and Hematological Values in Normal and Streptozotocin-Induced Diabetic Rats of Mimosa pudica L. Extracts</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Blood glucose level</style></keyword><keyword><style  face="normal" font="default" size="100%">Hematological values</style></keyword><keyword><style  face="normal" font="default" size="100%">Mimosa pudica</style></keyword><keyword><style  face="normal" font="default" size="100%">Red blood cell</style></keyword><keyword><style  face="normal" font="default" size="100%">White blood cell</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-3/10.5530pj.2017.3.54</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">315-322</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Context:&lt;/strong&gt;&amp;nbsp;&lt;em&gt;M. pudica&lt;/em&gt; is a common plant found in moist waste ground, lawns, open plantations and weedy thickets. &lt;strong&gt;Aims:&lt;/strong&gt; The fasting blood glucose levels (FBG) and hematological values of &lt;em&gt;M. pudica aqueous&lt;/em&gt;(MPA) and hydro-ethanolic (MPHE) extract were evaluated in normal and streptozotocin (STZ)-induced diabetic rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; MPA and MPHE 125, 250 and 500 mg/kg body weight (b.w.) were administered orally and daily to the rats for 8 weeks. The FBG were determined weekly. Red blood cells (RBC), hemoglobin (HM. pudicab), hematocrit (Hct), platelet, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), white blood cells (WBC), lymphocytes, monocytes, neutrophils and eosinophil were evaluated. &lt;strong&gt;Results:&lt;/strong&gt; MPA and MPHE had no effect on blood glucose levels in normal rats. All doses of all extracts showed significantly (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05) decreasing FBG in diabetic rats. Especially MPA at the dose of 250 mg/kg b.w. showed more potent significantly (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05) decreasing blood glucose levels than anti-diabetic drug glibenclamide at the end of experiment. All extracts had no effect on RBC, Hb, Hct, platelet, MCH, MCHC, lymphocytes, monocytes neutrophils and eosinophils. Surprisingly, the extracts were decreased WBC and MCV in diabetic rats. In addition, all of the extracts did not produce the alteration of blood cells structure in all rats. &lt;strong&gt;Conclusion:&lt;/strong&gt; This study indicated that the extracts were hypoglycemic effect and improve hematological values in diabetes which confirms the traditional use of the plant.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">315</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Ampa Konsue&lt;sup&gt;1&lt;/sup&gt;, Chayan Picheansoonthon&lt;sup&gt;2,3&lt;/sup&gt;, Chusri Talubmook&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Candidate, Faculty of Medicine, Mahasarakham University, Maha Sarakham, 44000, THAILAND.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Alternative Medicine College Chandrakasem Rajabhat University, Chatuchak, Bangkok 10900, THAILAND.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt; 3&lt;/sup&gt;The Academy of science, The Royal Institute Sanam Suea Pa Khet Dusti Bangkok 10300, THAILAND.&lt;/p&gt;
&lt;p&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biology, Faculty of Sciences, Mahasarakham University, Maha Sarakham 44150, THAILAND.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohamed Saleem Thattakudian Sheik Uduman</style></author><author><style face="normal" font="default" size="100%">Prema Rathinam</style></author><author><style face="normal" font="default" size="100%">Yogendrachari Karuru</style></author><author><style face="normal" font="default" size="100%">Gangadhar Obili</style></author><author><style face="normal" font="default" size="100%">Gopinath Chakka</style></author><author><style face="normal" font="default" size="100%">Ashok Kumar Janakiraman</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">GC-MS Analysis of Ethyl Acetate Extract of Whole Plant of Rostellularia diffusa</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Bioactive compounds</style></keyword><keyword><style  face="normal" font="default" size="100%">Gas chromatography</style></keyword><keyword><style  face="normal" font="default" size="100%">Mass spectrometry</style></keyword><keyword><style  face="normal" font="default" size="100%">phytosterol.</style></keyword><keyword><style  face="normal" font="default" size="100%">Rostellularia diffusa</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">70-72</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; To identify the various phyto constituents present in the unexplored plant &lt;em&gt;Rostellularia diffusa&lt;/em&gt; (Willd.) by using gas chromatography and mass spectrometry. &lt;strong&gt;Methods:&lt;/strong&gt; The whole plant of &lt;em&gt;Rostellularia diffusa &lt;/em&gt;was extracted with ethyl acetate at room temperature for 72 h. The concentrated extract was subjected to GCMS analysis to detect the phyto constituents. &lt;strong&gt;Results:&lt;/strong&gt; Totally 40 compounds were identified and the chromatograph showed 40 peaks with 40 individual compounds. The major constituents were identified in the extract were 16-Hentriacontanone (22.59%), Hexadecanoic acid (11.23%), Stigmast-5-en-3-ol (6.78%), 9-Octadecenoic acid (6.30%) and many other compounds were identified as low level. This preliminary study gives an idea to isolate the major active constituents present in the plant and also helps to develop potential pharmacologically active compounds&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">70</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Mohamed Saleem Thattakudian Sheik Uduman&lt;sup&gt;1*&lt;/sup&gt;, Prema Rathinam&lt;sup&gt;1&lt;/sup&gt;, Yogendrachari Karuru&lt;sup&gt;1&lt;/sup&gt;, Gangadhar Obili&lt;sup&gt;1&lt;/sup&gt;, Gopinath Chakka&lt;sup&gt;1&lt;/sup&gt;, Ashok Kumar Janakiraman&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Annamacharya College of Pharamcy, Rajampet, YSR Kadapa, A.P, INDIA.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, UCSI University, Kuala Lumpur, MALAYSIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sakshi Bajaj</style></author><author><style face="normal" font="default" size="100%">Sharad Wakode</style></author><author><style face="normal" font="default" size="100%">Washim Khan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">HPTLC Analysis and Antiproliferative Effect of Various Extracts of Swertia alata on Growth of Leishmania donovani Promastigotes in vitro</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antiproliferative</style></keyword><keyword><style  face="normal" font="default" size="100%">HPTLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Oleanolic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Quality control</style></keyword><keyword><style  face="normal" font="default" size="100%">Swertiamarin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/391</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s107-s116</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The present study was carried out to evaluate the quality control analysis and antiproliferative effects of petroleum ether, chloroform, ethanol and aqueous extracts of Swertia alata (family Gentianaceae) on Leishmania donovani. A basic, exact, quick and reproducible high performance thin layer chromatography (HPTLC) has been created for synchronous analysis of Oleanolic acid and Swertiamarin from S. alata. &lt;/p&gt;

Read more...</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s107</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Sakshi Bajaj&lt;sup&gt;1&lt;/sup&gt;*, Sharad Wakode&lt;sup&gt;2&lt;/sup&gt;, Washim Khan&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy and Phytochemistry, University of Delhi, DIPSAR, Sec-III, Pushp Vihar, M.B Road, Delhi-110017, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Professor, Department of Pharmaceutical Chemistry, University of Delhi, DIPSAR, Sec-III, Pushp Vihar, M.B Road, Delhi-110017, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Ph.D Scholar, Faculty of Pharmacy, Department of Pharmacognosy and Phytochemistry, Jamia Hamdard (Hamdard University), Hamdard Nagar, New Delhi - 110062, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Teeraporn Katisart</style></author><author><style face="normal" font="default" size="100%">Surapong Rattana</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hypoglycemic Activity of Leaf Extracts from Tiliacora triandra in Normal and Streptozotocin-Induced Diabetic Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hypoglycemic Effect</style></keyword><keyword><style  face="normal" font="default" size="100%">Streptozotocin-Induced Diabetic Rats.</style></keyword><keyword><style  face="normal" font="default" size="100%">Tiliacora triandra</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/pj-9-5/10.5530pj.2017.5.99/index.html</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">621-625</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Tiliacora triandra&lt;/em&gt; is a common plant found in southeast Asian countries. It is traditionally used as anti-pyrogenic agent. &lt;strong&gt;Objective:&lt;/strong&gt; The present study was aimed to investigate the hypoglycemic activities leaf extracts from &lt;em&gt;Tiliacora triandra&lt;/em&gt; (TTE) in normal and streptozotocin- induced diabetic rats. &lt;strong&gt;Methods:&lt;/strong&gt; TTE was prepared and daily and orally administered at dose of 300 mg/kg b.w. to the rats for 8 weeks. The body weight and blood glucose level were measured weekly. At the end of the experiments, blood samples were collected from cardiac puncture and analyzed for serum insulin levels. The pancreatic tissues were stained by hematoxylin-eosin for histo-pathological investigations. &lt;strong&gt;Results:&lt;/strong&gt; Normal and diabetic rats treated with TTE and glibenclamide tended to have an increased body weight. TTE significantly decreased the blood glucose level by 25.01 &amp;plusmn; 19.77% in week 3 in diabetic rats and similar to that of glibenclamide group (27.01 &amp;plusmn; 11.89%). However, the extracts slightly decreased the blood glucose level in normal rats by 9.48 &amp;plusmn; 2.14% in week 2. TTE significantly increased serum insulin level by 21.63 &amp;plusmn; 1.39 IU/mL in diabetic rats compared to the controls (10.63 &amp;plusmn; 0.37 IU/mL) but not in normal rats. In additions, TTE activated the regeneration of pancreatic Islets of Langerhans in diabetic rats which in turn stimulated insulin secretion. &lt;strong&gt;Conclusion:&lt;/strong&gt; TTE exhibits the hypoglycemic potential by stimulating insulin secretion from the pancreas.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">621</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Teeraporn Katisart&lt;sup&gt;1*&lt;/sup&gt;, Surapong Rattana&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biology, Faculty of Science, Mahasarakham University, THAILAND&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmaceutical chemistry and Natural Products Research Unit, Faculty of Pharmacy, Mahasarakham University, THAILAND&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Piyapong Yupparach</style></author><author><style face="normal" font="default" size="100%">Ampa Konsue</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hypoglycemic and Hypolipidemic Activities of Ethanolic Extract from Mimosa pudica L. in Normal and Streptozotocin-Induced Diabetic Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hypoglycemic</style></keyword><keyword><style  face="normal" font="default" size="100%">Hypolipidemic</style></keyword><keyword><style  face="normal" font="default" size="100%">Mimosa pudica</style></keyword><keyword><style  face="normal" font="default" size="100%">Oral glucose tolerance test.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/183</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">834-837</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Context:&lt;/strong&gt; &lt;em&gt;Mimosa pudica&lt;/em&gt; L. its unique property to collapse when touched and opens up. &lt;strong&gt;Aims:&lt;/strong&gt; To evaluate hypoglycemic and hypolipidemic activities of 80% ethanolic extract from whole plant of &lt;em&gt;Mimosa pudica&lt;/em&gt; L. (MPE) by measuring fasting blood glucose in normal and streptozotocin (STZ)-induced diabetic rats treated with MPE. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; An eight-week study using MPE was performed in normal and streptozotocin (STZ)-induced diabetic rats. Hypoglycemic activities in normal and STZ-induced diabetic rats and oral glucose tolerance test (OGTT) and biochemical data include total cholesterol (TC), triglycerides (TG), high-density lipoprotein (HDL) and low-density lipoprotein (LDL) of MPE were compared with glibenclamide, a standard anti-diabetic drug. &lt;strong&gt;Results:&lt;/strong&gt; OGTT showed that MPE did not decrease blood glucose both in normal and STZ-induced diabetic rats comparable to controls and glibenclamide treated rats. Moreover, MPE did not affect FBG in the normal rats. However, it significantly (&lt;em&gt;p&lt;/em&gt;&amp;lt;0.05) decreased FBG in the diabetic rats while MPE increased HDL and decreased TC, TG and LDL in the diabetic rats. &lt;strong&gt;Conclusions:&lt;/strong&gt; The results from this study confirmed the traditional use of &lt;em&gt;Mimosa pudica&lt;/em&gt; L. for the treatment of diabetes mellitus.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">834</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Piyapong Yupparach, Ampa Konsue&lt;sup&gt;*&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Faculty of Medicine, Mahasarakham University, Maha Sarakham, 44000, THAILAND.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rudra Pratap Singh</style></author><author><style face="normal" font="default" size="100%">Gangadharappa H.V.</style></author><author><style face="normal" font="default" size="100%">Mruthunjaya K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">&lt;i&gt;Cuminum cyminum&lt;/i&gt; – A Popular Spice: An Updated Review</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cumin</style></keyword><keyword><style  face="normal" font="default" size="100%">Cuminaldehyde</style></keyword><keyword><style  face="normal" font="default" size="100%">Cymene</style></keyword><keyword><style  face="normal" font="default" size="100%">Spice</style></keyword><keyword><style  face="normal" font="default" size="100%">Thymol</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2017 </style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-3/10.5530pj.2017.3.51</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">292-301</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;Spices are bio-nutrient supplements that enhance the taste, flavor and aroma of food and also treat several diseases. Cumin (&lt;em&gt;Cuminum cyminum&lt;/em&gt;) is one such most popular spice that is used as a culinary spice for their special aromatic effect. Cumin is a traditional and much used spice from Middle Ages because it was an icon of love and fidelity. Cumin is available in different appearances such as anise, fennel and black cumin and the difference between them is their characteristics. The proximate analysis of the cumin seeds reveals that they contain fixed oil, volatile oils, acids, essential oils, protein and other elements. In cumin, contains an important component such as pinene, cymene, terpinene, cuminaldehyde, oleoresin, thymol and others that have shown their uses according to the disease. Cumin has proved several benefits with the help of availability of nutrients. It is an important element of iron for energy, immunity systems, lactation and skin diseases. Cumin also shown various pharmacological effects but has some side effects. So, volatile plants generally come out as a complex mixture of less molecular weight lipophilic compounds that derived from different biosynthetic pathways and also contribute to a variety of physiological functions.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Review article</style></work-type><section><style face="normal" font="default" size="100%">292</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Rudra Pratap Singh, Gangadharappa H.V.*, Mruthunjaya K &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Pharmaceutics, JSS College of Pharmacy, JSS University, Sri Shivarathreeshwara Nagar, Mysuru, Karnataka, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sunil Kumar</style></author><author><style face="normal" font="default" size="100%">Gaurav Sharma</style></author><author><style face="normal" font="default" size="100%">Amit Kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Immunomodulatory Activity of Bioactive Fraction (PBC) from Phyllostachys bambusoides</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cytokine.</style></keyword><keyword><style  face="normal" font="default" size="100%">Ha Titre</style></keyword><keyword><style  face="normal" font="default" size="100%">Immunostimulation</style></keyword><keyword><style  face="normal" font="default" size="100%">Macrophages</style></keyword><keyword><style  face="normal" font="default" size="100%">Phyllostachys Bambusoides</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/176</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">786-791</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; The lack of vaccines and limitations of currently available strategies demand a need to develop safe and efficacious immunomodulators. &lt;em&gt;Phyllostachys bambusoides&lt;/em&gt; is traditionally used for various autoimmune and infectious disorders, a property possibly attributable to presence of flavonoids like orientin and iso-orientin. &lt;strong&gt;Objective:&lt;/strong&gt; the objective of this study was, to search a potent immunomodulator which elicit both Th1 and Th2 immune response. &lt;strong&gt;Methods:&lt;/strong&gt; The animals were (Balb/c) treated with the bioactive fraction (PBC) from &lt;em&gt;P. bambusoides&lt;/em&gt; (100 and 200 mg/kg body weight) for 14 days with SRBC (Sheep Red Blood Cells) as an antigen. Haemagglutination antibody (HA) titre, delayed type hypersensitivity (DTH) reaction, phagocytic index, NO production, analysis of cytokines in serum and CD80/ CD86 population in spleen. &lt;strong&gt;Results:&lt;/strong&gt; PBC significantly enhanced the expression of IgM and IgG titre and DTH response in a dose dependant manner after 24 and 48 h in BALB/c mice with a maximum response at 200 mg/Kg. Besides humoral and cell mediated immunity, it also enhanced phagocytic index, nitric oxide production, which further leads to protection against &lt;em&gt;Candida albicans&lt;/em&gt; infection. It also, enhanced the expression of CD80 and CD86 in splenic cells. &lt;strong&gt;Conclusion:&lt;/strong&gt; Taken together these i&lt;em&gt;n vitro&lt;/em&gt; and &lt;em&gt;in vivo&lt;/em&gt; data, our results suggest that PBC acts as an effective immunostimulator which specially enhances macrophage function during infection. This further supports the role of PBC in immunopharmacologic applications.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">786</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Sunil Kumar&lt;sup&gt;1*&lt;/sup&gt;, Gaurav Sharma&lt;sup&gt;1&lt;/sup&gt;, Amit Kumar&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, School of Pharmaceutical Sciences Shoolini University Solan,  Himachal Pradesh 173229, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Indian Institute of Integrative Medicine (CSIR), Jammu 180001, Jammu and
Kashmir, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Preetham Jinadatta</style></author><author><style face="normal" font="default" size="100%">Kiran Sundera Raja Rao</style></author><author><style face="normal" font="default" size="100%">Sharath Rajshekarappa</style></author><author><style face="normal" font="default" size="100%">Sujan Ganapathy Pasura Subbaiah</style></author><author><style face="normal" font="default" size="100%">Mruthunjaya Kenganora</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In vitro Antioxidant and Hepatoprotective Activity of Bridelia scandens (Roxb.)Willd</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Bridelia scandens</style></keyword><keyword><style  face="normal" font="default" size="100%">BRL3A</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatoprotective</style></keyword><keyword><style  face="normal" font="default" size="100%">MTT</style></keyword><keyword><style  face="normal" font="default" size="100%">ORAC</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/392</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s117-s121</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;Natural products are emerging out as potent and alternative therapies for many diseases. Today herbs have become the part of mankind, because of its manifold ways in targeting diseased cells with minimal effects on normal cells and tissues. The present research investigated the &lt;em&gt;in vitro&lt;/em&gt; antioxidant activity and hepatoprotective of &lt;em&gt;B.scandens&lt;/em&gt; leaf. Preliminary phytochemical analysis exhibited the presence of most of the constituent in ethanol extract (BSE). Antioxidant capacity of various extracts of &lt;em&gt;B.scandens&lt;/em&gt; was examined. DPPH assay revealed that ethanol extract has a good antioxidant with IC&lt;sub&gt;50&lt;/sub&gt; value of 31.68&amp;mu;g/ml, whereas standard ascorbic acid with 8.78 &amp;mu;g/ml. BSE revealed dose dependent response with increase in concentration for reducing power assay. ORAC assay directly measured the scavenging capacity and BSE (2485 trolox eq/gm) was found to be potent than other extracts. &lt;em&gt;In vitro&lt;/em&gt; hepatoprotective activity was performed for BSE using MTT assay in BRL 3A cell line, which revealed nontoxic dose with CTC&lt;sub&gt;50&lt;/sub&gt; value more than 1000 &amp;mu;g/ml. At the dose 200 &amp;mu;g/ml, BSE and standard silymarin offered cell protection of 57% and 76 % respectively. Present study concludes that &lt;em&gt;B.scandens&lt;/em&gt; leaf extract possess antioxidant potential and protect the liver cells against CCl&lt;sub&gt;4&lt;/sub&gt; damage. However in vivo studies are being carried out to validate the traditional usage of &lt;em&gt;Bridelia scandens&lt;/em&gt;.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s117</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Preetham Jinadatta&lt;sup&gt;1&lt;/sup&gt;*, Kiran Sundera Raja Rao&lt;sup&gt;1&lt;/sup&gt;, Sharath Rajshekarappa&lt;sup&gt;2&lt;/sup&gt;, Sujan Ganapathy Pasura Subbaiah&lt;sup&gt;3&lt;/sup&gt;, Mruthunjaya Kenganora&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biotechnology, Dayananda Sagar College of Engineering, Kumaraswamy Layout, Bangalore-560078, Karnataka, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biotechnology, M.S. Ramaiah Institute of Technology, MSRIT Post Bangalore 560054, Karnataka, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Research and Development Centre, Indusviva International Private Limited, No.7450, Near Navayuga Toll Gate Office, NH-4, Nelamangala, Bangalore &amp;ndash; 562123, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacognosy, JSS College of Pharmacy, JSS University, Mysuru-570015 Karnataka, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Srikanth Jeyabalan</style></author><author><style face="normal" font="default" size="100%">Kavimani Subramanian</style></author><author><style face="normal" font="default" size="100%">Uma Maheswara Reddy Cheekala</style></author><author><style face="normal" font="default" size="100%">Chitra Krishnan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In vitro &amp; ex vivo Acetylcholinesterase Inhibitory Activity of Morinda citrifolia Linn (Noni) Fruit Extract</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acetylcholinesterase</style></keyword><keyword><style  face="normal" font="default" size="100%">ex vivo.</style></keyword><keyword><style  face="normal" font="default" size="100%">in vitro</style></keyword><keyword><style  face="normal" font="default" size="100%">Morinda citrifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">Neuroprotective activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Noni</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/194</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">900-905</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Psychological problem is a key medical issue for numerous neuropsychiatric and neurodegenerative diseases, for example, schizophrenia, Alzheimer&amp;rsquo;s, dementia, seizure and Parkinsonism. &lt;em&gt;Morinda citrifolia&lt;/em&gt; (Noni) has been utilized for a considerable length of time to cure or counteract assortment of diseases by conventional therapeutic professionals in Hawaii and Polynesia. &lt;strong&gt;Objective:&lt;/strong&gt; The present study is focused to identify the neuroprotective activity of &lt;em&gt;Morinda citrifolia &lt;/em&gt;fruit extract (MCFE) on &lt;em&gt;in vitro&lt;/em&gt; and ex vivo animal model by inhibition of acetylcholinesterase (AChE), an enzyme target used for the treatment of Alzheimer&amp;rsquo;s disease. &lt;strong&gt;Methods:&lt;/strong&gt; Acetylcholinesterase inhibition assay was performed by &lt;em&gt;in vitro&lt;/em&gt; &amp;amp; &lt;em&gt;ex vivo&lt;/em&gt; methods as described by Ellman et al.&lt;em&gt; In vitro&lt;/em&gt; antioxidant assay of the extract was performed by DPPH free radical scavenging activity &amp;amp; nitric oxide scavenging activity. &lt;strong&gt;Statistical analysis used:&lt;/strong&gt; Statistical analysis was carried out using non linear regression analysis for plotting the line of best fit for the observed values using Graph- Pad Prism software. &lt;strong&gt;Results:&lt;/strong&gt; By performing &lt;em&gt;in vitro&lt;/em&gt; antioxidant assay the IC&lt;sub&gt;50&lt;/sub&gt; value of the standard quercetin was found to be 46.22 &amp;mu;g/ml as compared to the MCFE which has an IC&lt;sub&gt;50&lt;/sub&gt; value of 43.14 &amp;mu;g/ml for DPPH free radical scavenging activity. Similarly the IC&lt;sub&gt;50&lt;/sub&gt; value of the standard ascorbic acid was found to be 81.85 &amp;mu;g/ml as compared to the MCFE which has an IC&lt;sub&gt;50&lt;/sub&gt; value of 148.0 &amp;mu;g/ml for nitric oxide scavenging activity. Acetylcholinesterase inhibition assay was performed by &lt;em&gt;in vitro&lt;/em&gt; method and the IC&lt;sub&gt;50&lt;/sub&gt; value of MCFE and neostigmine was found to be 31.84 &amp;mu;g/ml &amp;amp; 19.71 &amp;mu;g/ml respectively. Conclusions: The present study investigated the neuroprotective activity of MCFE and it was identified by both &lt;em&gt;in vitro&lt;/em&gt; and&lt;em&gt; ex vivo&lt;/em&gt; techniques that the phytoconstituents has the ability to improve the learning and memory function by inhibiting the acetylcholinesterase.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">900</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Srikanth Jeyabalan&lt;sup&gt;1*&lt;/sup&gt;, Kavimani Subramanian&lt;sup&gt;2&lt;/sup&gt;, Uma Maheswara Reddy Cheekala&lt;sup&gt;3&lt;/sup&gt;, Chitra Krishnan&lt;sup&gt;4&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Faculty of Pharmacy, Sri Ramachandra University, Porur, Chennai &amp;ndash; 600 116, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology, Mother Theresa Post Graduate and Research Institute of Health Sciences, Puducherry - 605006, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacology, Faculty of Pharmacy, Sri Ramachandra University, Porur, Chennai &amp;ndash; 600 116, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmaceutical chemistry, Faculty of Pharmacy, Sri Ramachandra University, Porur, Chennai &amp;ndash; 600 116, Tamil Nadu, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Endang Hanani</style></author><author><style face="normal" font="default" size="100%">Rini Prastiwi</style></author><author><style face="normal" font="default" size="100%">Lina Karlina</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Indonesian Mirabilis jalapa Linn. : A Pharmacognostical and Preliminary Phytochemical Investigations</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Chromatography Profile</style></keyword><keyword><style  face="normal" font="default" size="100%">Flourescence Character</style></keyword><keyword><style  face="normal" font="default" size="100%">Microscopic</style></keyword><keyword><style  face="normal" font="default" size="100%">Nyctaginaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Physicochemical</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/pj-9-5/10.5530pj.2017.5.108/index.html</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">683-688</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Mirabilis jalapa Linn.&lt;/em&gt; is an important medicinal plant and used extensively by the people from different countries for the treatment of several disorders. The plant was the raw material for the herb-drug product, so some parameters identified were needed to ensure the safety, quality and efficacy of the product. &lt;strong&gt;Objective:&lt;/strong&gt; The aim of this study was to undertake pharmacognostical studies to fulfill the work required for the identification the &lt;em&gt;M. jalapa&lt;/em&gt; plant, which is collected from the Bogor area, Indonesia. &lt;strong&gt;Methods:&lt;/strong&gt; Macroscopic and microscopic evaluation, fluorescence standards, phytochemical screening and physicochemical parameters were carried out on the above plant. &lt;strong&gt;Results:&lt;/strong&gt; The parameters values of total ash, water soluble and acid insoluble ash were obtained 11.81, 5.06 and 0.41%, respectively. Moisture content, alcohol, water and ether soluble extractive were found to be 12.41, 11.02, 18.63 and 7.17% respectively. The results of preliminary phytochemical analysis of aqueous ethanolic extract of this drug were positive for alkaloids, tannins, flavonoids, steroid, triterpenoids, saponin, phenols, glycosides and carbohydrate. Thin layer chromatography (TLC) of alcoholic, chloroform and aqueous extracts showed 9, 7 and 4 spots respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; The present study on botanical pharmacognosy and TLC profile of this plant above thus provides useful information for correct identification and quality control parameters for the crude drugs, and also will be useful in making monograph of the plant.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">683</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Endang Hanani*, Rini Prastiwi, Lina Karlina &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Faculty of Pharmacy and Sciences, University of Muhammadiyah Prof. Dr. HAMKA Jl. Delima II/IV Klender, Jakarta 13460, INDONESIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aswathy Jayasree Madanakumar</style></author><author><style face="normal" font="default" size="100%">Greeshma Murukan</style></author><author><style face="normal" font="default" size="100%">Bosco Lawarence</style></author><author><style face="normal" font="default" size="100%">Murugan Kumaraswamy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Isolation, Purification of Quercetin from in vitro Cell Suspension Culture of Caesalpinia pulcherrima and its Analysis by HPLC-DAD and NMR</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Caesalpinia pulcherrima</style></keyword><keyword><style  face="normal" font="default" size="100%">Callus</style></keyword><keyword><style  face="normal" font="default" size="100%">Cell suspension culture</style></keyword><keyword><style  face="normal" font="default" size="100%">Elicitors; growth hormones</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercetin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/380</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s44-s51</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Caesalpinia pulcherrima&lt;/em&gt;, belongs to Caesapiniaceae, is a known medicinal plant widely distributed in India and is used in traditional medicine for the treatment of various ailments. Many phytochemicals are reported from the plant as potential source of crude drug. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; An efficient and simple reproducible protocol was developed for callus production using leaf explants of &lt;em&gt;C. pulcherrima&lt;/em&gt;. The combination of 2, 4-D, kin and BA, was used for the callus induction. Subsequently, cell suspension culture and quercetin synthesis from &lt;em&gt;in vitro&lt;/em&gt; callus was attempted. Role of effect of elicitors (Sucrose, ABA and salicylic acid) in cell suspension culture was carried in MS medium containing 2,4-D + BA + kinetin. Flavonoids was purified, fractionated by HPLC-DAD and NMR.&lt;strong&gt; Results:&lt;/strong&gt; 2, 4-D (2.5 mg/L), BA (2.5 mg/L) + kin (1 mg/mL) was effective for maximum callus induction from leaf explants. Significant cell suspension culture was noticed with liquid MS medium containing 2,4-D (2 mg/L)+ BA (1mg/L)+ kinetin (1.5 mg/L). Sucrose, ABA and salicylic acid (SA) at different concentrations influenced cell biomass and quercetin accumulation. The addition of ABA/SA along with sucrose was found to have no remarkable effect on cell biomass and also quercetin synthesis. However, cells cultured in the medium fortified with 45 g/L sucrose without ABA/ SA showed the highest quercetin content (16.5 mg/g). Flavonoids was purified, fractionated by HPLC-DAD and NMR revealed the presence of 9 components such as quercetin, isoquercetin, quercetrin, rutin, quercetin 3-O-&amp;beta;-D-xyloside, quercetin 3-Oarabinopyranoside, quercetin 3-O- &amp;alpha;-arabinopyranosyl (1&amp;rarr;2) &amp;beta;-galactopyranoside, isorhamnetin 3-O-rutinoside and an unknown compound. &lt;strong&gt;Conclusion:&lt;/strong&gt; &lt;em&gt;C. pulcherima&lt;/em&gt; reveals significant synthesis of quercetin. Quercetin content recorded in cell suspension culture was significantly higher compared with &lt;em&gt;in vivo&lt;/em&gt; plants grown in fields and the compounds were identified by NMR.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s44</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aswathy Jayasree Madanakumar, Greeshma Murukan, Bosco Lawarence, Murugan Kumaraswamy* &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Plant Biochemistry and Molecular Biology Laboratory, University College, Trivandrum, Kerala, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Somanjana Khatua</style></author><author><style face="normal" font="default" size="100%">Sandipta Ghosh</style></author><author><style face="normal" font="default" size="100%">Krishnendu Acharya</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Laetiporus sulphureus (Bull.: Fr.) Murr. as Food as Medicine</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Bioactive components</style></keyword><keyword><style  face="normal" font="default" size="100%">Commercial Importance</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethnic Relevance</style></keyword><keyword><style  face="normal" font="default" size="100%">Nutritious Food</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacological Effects</style></keyword><keyword><style  face="normal" font="default" size="100%">“Chicken of the Woods”</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/374</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s1-s15</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;em&gt;Laetiporus sulphureus&lt;/em&gt; is a sulphur yellow coloured polyporous mushroom and popularly known as &amp;ldquo;chicken of the woods&amp;rdquo;. Over the generations, this cosmopolitan macrofungus has become an integral part of tribal cuisines particularly for its taste. Besides, it has equal importance in folk medicine being widely used for treatment of pyretic diseases, coughs, gastric cancer and rheumatism. Thus, the species is considered as a natural reservoir of both nourishment as well as drug therapy and consequently it has become increasingly popular in scientific world. Nutritional sciences recently have witnessed it as a sustainable food supply to growing population due to enrichment of carbohydrate (trehalose&amp;gt; mannitol&amp;gt; fructose), protein (histidine, isoleucine, leucine, lysine, methionine, threonine), minerals (calcium, phosphorus, magnesium, sodium, potassium, iron, zinc, manganese, copper), vitamins (B, D, E), polyunsaturated fatty acids (linoleic acid, oleic acid, palmitic acid) and fibre. Conversely, the mushroom has also been regarded as an abundant source of chemical compounds including phenolics, triterpenes, polysaccharides with wide range of biological activities such as antiinflammatory, antimicrobial, antioxidant, antihyperglycemic, antitumor and immunomodulation effects. Therefore, a complete summary of the research progress on this fungus is necessary for further studies and commercial exploitation. In this context, the present review attempts to congregate current knowledge on nutritional value, myco-chemistry and therapeutic potential of this culturally important species. However, investigation on bioavailability, quality control, toxicology data and clinical assessment are highly recommended for future research.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">s1</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Somanjana Khatua, Sandipta Ghosh, Krishnendu Acharya* &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Molecular and Applied Mycology and Plant Pathology Laboratory, Department of Botany, University of Calcutta, 35, Ballygunge Circular Road, Kolkata, 700019, West Bengal, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Morvin Yabesh Jobu Esther</style></author><author><style face="normal" font="default" size="100%">Vijayakumar Subramaniyan</style></author><author><style face="normal" font="default" size="100%">Arulmozhi Praveen Kumar</style></author><author><style face="normal" font="default" size="100%">Mahadevan Subramanian</style></author><author><style face="normal" font="default" size="100%">Manogar Palani</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular Docking, ADMET Analysis and Dynamics Approach to Potent Natural Inhibitors against Sex Hormone Binding Globulin in Male Infertility</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ADMET property</style></keyword><keyword><style  face="normal" font="default" size="100%">Male infertility</style></keyword><keyword><style  face="normal" font="default" size="100%">MD simulations</style></keyword><keyword><style  face="normal" font="default" size="100%">Molecular docking</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytocompounds</style></keyword><keyword><style  face="normal" font="default" size="100%">SHBG</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/379</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s35-s43</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objectives:&lt;/strong&gt; The Sex Hormone Binding Globulin (SHBG) plays an important role in male infertility. &lt;strong&gt;Methods:&lt;/strong&gt; The present research computationally emphases to SHBG protein with 47 natural phytocompounds using docking studies. &lt;strong&gt;Results:&lt;/strong&gt; From the results showed the interactions between 1KDM protein with 47 phytocompounds, a natural compound chlorogenic acid showed the best glide docking XP score -7.255 kcal/mol and the binding energy value of -47.869 kcal/ mol. Based on the result, the chlorogenic acid and target were run on MD simulations stable at 10 ns. &lt;strong&gt;Conclusion:&lt;/strong&gt; Finally, this study concludes the chlorogenic acid is a suitable drug candidate for infertility.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s35</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Morvin Yabesh Jobu Esther*, Vijayakumar Subramaniyan, Arulmozhi Praveen Kumar, Mahadevan Subramanian and Manogar Palani &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Computational Phytochemistry Lab, PG and Research Department of Botany and Microbiology, AVVM Sri Pushpam College (Autonomous), Poondi, Thanjavur, Tamil Nadu, India&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fatima Kazbekovna Serebrynaya</style></author><author><style face="normal" font="default" size="100%">Naida Mahmudovna Nasuhova</style></author><author><style face="normal" font="default" size="100%">Dmitryi Alexeevich Konovalov</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Morphological and Anatomical Study of the leaves of Laurus nobilis L. (Lauraceae), growing in the Introduction of the Northern Caucasus region (Russia)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anatomical Structure of Leaf</style></keyword><keyword><style  face="normal" font="default" size="100%">Essential Oil.</style></keyword><keyword><style  face="normal" font="default" size="100%">Laurus Nobilis</style></keyword><keyword><style  face="normal" font="default" size="100%">Morphological and Anatomical Study</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-4/10.5530pj.2017.4.83</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">519-522</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;In this article results of morphological and anatomical research &lt;em&gt;Laurus nobilis&lt;/em&gt; L. are resulted. These plants are growing in the conditions of culture in the Botanical garden of Pyatigorsk medical and pharmaceutical institute (Northern Caucasus region). &lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Laurus nobilis&lt;/em&gt; L. is grown up as a decorative species in Europe, RUSSIA, the USA and other countries. Chemical composition of the leaves is characterized by essential oil components, sesquiterpene lactones, phenolic and other compounds.&lt;strong&gt; Material And Methods:&lt;/strong&gt; Micro morphological research of vegetative bodies was carried out with the help of a well-known technique. We carry out morphological and anatomical research of a leaf blade and a petiole of a leaf of a plant, which is grown up in a Botanical garden in the Pyatigorsk medical and pharmaceutical institute. &lt;strong&gt;Results:&lt;/strong&gt; The diagnostic characteristics of a leaf blade necessary for an establishment of authenticity of raw materials are revealed. The leaf is hypostomal, dorsoventral, stomatal apparatus of paracytic type. The idioblasts with the essential oil are obtained between mesophyll cells. Idioblasts thin-walled, large enough. In the field of the main vein under an epidermis the collenchyma of lamellar type in 4-7 layers settles down. The leaf petiole on cross-section section has the saddle-like form, without a ledge on the abaxial side of leaf. Under an epidermis the parenchyma settles down, is presented by live cells of the roundish or oval form. Between parenchyma cells it is possible to observe numerous cells-idioblasts with contents of yellow colour. &lt;strong&gt;Conclusions:&lt;/strong&gt; As diagnostic signs of leaf (a leaf blade and a petiole) it is possible to consider numerous cells - idioblasts with an essential oil, the leaf is &lt;em&gt;hypostomatical,&lt;/em&gt; dorsoventral, stomatal apparatus of paracytic type. The idioblasts with the essential oil are obtained between mesophyll cells.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">519</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Fatima Kazbekovna Serebrynaya*, Naida Mahmudovna Nasuhova, Dmitryi Alexeevich Konovalov &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Botany and Department of Pharmacognozy, Pyatigorsk Medical and Pharmaceutical Institute, a branch of Volgograd State Medical University Ministry of Health of the Russian Federation, Pyatigorsk, 357532, Kalinina Av.11, RUSSIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Karim Raafat</style></author><author><style face="normal" font="default" size="100%">Rawan El-Haj</style></author><author><style face="normal" font="default" size="100%">Dania Shoumar</style></author><author><style face="normal" font="default" size="100%">Rana Alaaeddine</style></author><author><style face="normal" font="default" size="100%">Yousra Fakhro</style></author><author><style face="normal" font="default" size="100%">Natalie Tawil</style></author><author><style face="normal" font="default" size="100%">Farah Shaer</style></author><author><style face="normal" font="default" size="100%">Amani Daher</style></author><author><style face="normal" font="default" size="100%">Natalie Awada</style></author><author><style face="normal" font="default" size="100%">Ali Sabra</style></author><author><style face="normal" font="default" size="100%">Khouloud Atwi</style></author><author><style face="normal" font="default" size="100%">Malak Khaled</style></author><author><style face="normal" font="default" size="100%">Raneem Messi</style></author><author><style face="normal" font="default" size="100%">Nour Abouzaher</style></author><author><style face="normal" font="default" size="100%">Mohamed Houri</style></author><author><style face="normal" font="default" size="100%">Samer Al Jallad</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Neuropathic Pain: Literature Review and Recommendations of Potential Phytotherapies</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Current therapies</style></keyword><keyword><style  face="normal" font="default" size="100%">Diagnosis</style></keyword><keyword><style  face="normal" font="default" size="100%">Mechanisms</style></keyword><keyword><style  face="normal" font="default" size="100%">Neuropathy Pain</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytotherapies</style></keyword><keyword><style  face="normal" font="default" size="100%">Recommendations</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-4/10.5530pj.2017.4.72</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">425-434</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; One of the common syndromes that affect humanity is neuropathic pain (NP), yet poorly understood with no efficient treatment till now. Consequently, it is extremely crucial to seek further evidence for accurate diagnosis and optimum treatment. The aim of this work is to summarize the findings related to neuropathic pain in terms of etiology, types, diagnosis, current and future management prospective, and identify the gaps in neuropathic pain therapy. &lt;strong&gt;Methods:&lt;/strong&gt; A literature investigation was carried out by analyzing classical peer reviewed papers and textbooks, taking into consideration worldwide well established scientific databases mainly PUBMED and SCOPUS to retrieve accessible published literature. The selection of phytotherapies was based upon their potentials in relieving NP in pre-clinical or clinical models. &lt;strong&gt;Results:&lt;/strong&gt; One of the most critical points in this research is that recommendations of the future plans should be focused on the engagement of phytotherapy in the treatment regimen aiming at improving patients&amp;rsquo; quality of life and reaching optimum efficacy and minimum toxicity. Phytotherapies offer relatively low-risk options to NP patients and have an increasing evidence to be the future of neuropathic pain management. Patients suffering from neuropathy are depending increasingly on phytotherapies; however, they need more clinical trials in order to fully understand their mechanism of actions. &lt;strong&gt;Conclusion:&lt;/strong&gt; Health-care specialists should be regularly informed about neuropathic pain current therapies and promising future phytotherapies, bearing in mind the risk/benefit profile of the utilization of these therapies in the amelioration of NP.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">425</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Karim Raafat&lt;sup&gt;*&lt;/sup&gt;, Rawan El-Haj, Dania Shoumar, Rana Alaaeddine, Yousra Fakhro, Natalie Tawil, Farah Shaer, Amani Daher, Natalie Awada, Ali Sabra, Khouloud Atwi, Malak Khaled, Raneem Messi, Nour Abouzaher, Mohamed Houri and Samer Al Jallad &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Pharmaceutical Sciences, Faculty of Pharmacy, Beirut Arab University, 115020 Beirut, LEBANON,&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Umbreen Khattak</style></author><author><style face="normal" font="default" size="100%">Rehman Ullah</style></author><author><style face="normal" font="default" size="100%">Shafqat Ali Khan</style></author><author><style face="normal" font="default" size="100%">Barkatullah</style></author><author><style face="normal" font="default" size="100%">Sami Ullah</style></author><author><style face="normal" font="default" size="100%">Saima</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic Evaluation and Analgesic Efficacy of Ethanolic Extract of Euphorbia dracunculoides L.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Analgesic activity.</style></keyword><keyword><style  face="normal" font="default" size="100%">Euphorbia Dracunculoides L. Macroscopic Study</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognostic evaluation</style></keyword><keyword><style  face="normal" font="default" size="100%">Physio chemical Analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Powder Drug Study</style></keyword><keyword><style  face="normal" font="default" size="100%">Whole plant</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/pj-9-5/10.5530pj.2017.5.102/index.html</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">644-653</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Euphorbia dracunculoides&lt;/em&gt; L is available in market in raw form. It is used by people for the treatment of warts, snake bite and epilepsy. Present study is about &lt;em&gt;Euphorbia dracunculoides&lt;/em&gt; L. belonging to the family Euphorbiaceae, comprises pharmacognostic study, physiochemical analysis and their pharmacological efficacy. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The macroscopic study was carried out through sensory organs like size, shape, texture etc. Physiochemical analysis was carried out through proper procedure from relevant literature, and analgesic activity was done through proper method by following literature. &lt;strong&gt;Results:&lt;/strong&gt; Macroscopic study showed that the plant is an annual herb, stem is branched from the base, yellow green at the bottom and light green at the top, glabrous, smooth, contains white latex, its leaves are sessile, alternate, dark green, simple, stipulated, sub-acute or acute at the apex and entire margin. Root is yellowish in colour, conical in shape, smooth texture, downward in position. Powder drug study which was performed revealed various structures. Phytochemical screening includes both qualitative and quantitative analysis which was carried out indicated the presence of carbohydrates, proteins, saponins, sterols, alkaloids, phenolic compounds, glycosides, flavonoids and tannins. Proximate analysis showed proteins, crude fat, crude fibre, carbohydrates, moisture contents and ash. Elemental analysis revealed the presence of macro and micronutrients i-e Na, Zn, Mg and Fe, Cu, Ag and Au. Analgesic effect was dose dependent. Plant extract showed maximum inhibition of writhing 1.66&amp;plusmn;0.32 (96.61%) at 300 &amp;mu;g/ml. &lt;strong&gt;Conclusion:&lt;/strong&gt; The pharmacognostic study, physiochemical analysis and their pharmacological efficacy is helpful in the standardization of drug.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">644</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Umbreen Khattak,&lt;sup&gt;1&lt;/sup&gt; Rehmanullah,&lt;sup&gt;2&lt;/sup&gt; Shafqat Ali Khan,&lt;sup&gt;*1&lt;/sup&gt; Barkatullah,&lt;sup&gt;1&lt;/sup&gt; Sami Ullah&lt;sup&gt;2 &lt;/sup&gt; and Saima&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Botany, Islamia College University, Peshawar, PAKISTAN.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Botany, University of Peshawar, PAKISTAN.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prashant Kumar</style></author><author><style face="normal" font="default" size="100%">Abhishek Gupta</style></author><author><style face="normal" font="default" size="100%">Anita Singh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic Evaluation and Determination of Secondary Plant Metabolites by HPTLC and its Antioxidant Activity in Myrica esculenta</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">Gallic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">HPTLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Myrica Esculenta</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/390</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s103-s106</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Myrica esculenta&lt;/em&gt; Buch.-Ham. (Myricaceae) is commonly known as Box Berry, Kaiphal, and Katphala in Ayurveda. As per the Ayurvedic literature the palnt is used for variety of diseases and disorders. &lt;strong&gt;Method:&lt;/strong&gt; The present study deals with the pharmacognostical standardization, HPTLC analysis and antioxidant activity of methanolict extracts of the leaves of &lt;em&gt;M. esculenta&lt;/em&gt;. The plant showed high phenolic and flavonoid content. &lt;em&gt;In-vitro&lt;/em&gt; antioxidant study of dried leaves of &lt;em&gt;Myrica esculanta&lt;/em&gt; was performed using methanolic extract. &lt;strong&gt;Results:&lt;/strong&gt; Antioxidant activity of &lt;em&gt;M. esculenta&lt;/em&gt; methanolic extract showed the least IC&lt;sub&gt;50&lt;/sub&gt; value of 60 &amp;plusmn; 1.15 &amp;mu;g/ml. Standard ascorbic acid showed an IC&lt;sub&gt;50&lt;/sub&gt; value of 2.03 &amp;plusmn; 0.06 &amp;mu;g/ml. The calibration curve of Gallic acid showed r&lt;sup&gt;2&lt;/sup&gt; of 0.949 and R&lt;sub&gt;f&lt;/sub&gt; of gallic acid was found to be 0.44 &amp;plusmn; 0.006. Quantification of gallic acid in the samples of leaves of &lt;em&gt;M. esculenta &lt;/em&gt;has been performed and the gallic acid was found to be 0.056%. &lt;strong&gt;Conclusion:&lt;/strong&gt; The presence of gallic acid has not yet been reported and quantified in this species which may be utilized for the proper standardization of the drug. The present study showed new natural antioxidant that can replace the synthetic ones to be used in foods and cosmetics.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s103</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Prashant Kumar&lt;sup&gt;1&lt;/sup&gt;, Abhishek Gupta&lt;sup&gt;2&lt;/sup&gt;, Anita Singh&lt;sup&gt;1&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Sciences Kumaun University Bhimtal, Uttarakhand, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacognosy &amp;amp; Ethnopharmacology Division, CSIR-NBRI, Lucknow, INDIA.&amp;nbsp;&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mamta Arora</style></author><author><style face="normal" font="default" size="100%">Gurjinder Kaur</style></author><author><style face="normal" font="default" size="100%">Parvinderdeep S Kahlon</style></author><author><style face="normal" font="default" size="100%">Anupama Mahajan</style></author><author><style face="normal" font="default" size="100%">Jaspreet K Sembi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic Evaluation &amp; Antimicrobial Activity of Endangered Ethnomedicinal Plant Crepidium acuminatum (D. Don) Szlach</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimicrobial</style></keyword><keyword><style  face="normal" font="default" size="100%">Crepidium acuminatum (D. Don) Szlach</style></keyword><keyword><style  face="normal" font="default" size="100%">Histochemical</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognostic evaluation</style></keyword><keyword><style  face="normal" font="default" size="100%">Physicochemical</style></keyword><keyword><style  face="normal" font="default" size="100%">Zone of Inhibition</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/382</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s56-s63</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Crepidium acuminatum&lt;/em&gt; (D. Don) Szlach (family Orchidaceae) is an ethnomedicinal plant. It is used in breathing disorders, burning sensation, Cough, decrease in bone tissue, blood disorders, tuberculosis, as refrigerant, aphrodisiac, in insect bites, rheumatism, as tonic and in general debility. It is vital component of Ayurvedic formulation &amp;ldquo;Astavarga&amp;rdquo; with trade name &amp;ldquo;Jeevak means vitality of life. Despite the common utilization of this plant, no conclusive study has been reported so far regarding the pharmacognostic evaluation and antimicrobial activity. &lt;strong&gt;Aim:&lt;/strong&gt; The present study was carried to evaluate pharmacognostic evaluation and the potential of &lt;em&gt;C. acuminatum&lt;/em&gt; as antimicrobial. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Organoleptic, histochemical, microscopic, physicochemical, extractive yield were studied to standardise pharmacognostic characters and well diffusion method were carried out for antimicrobial activity. Five extracts viz. Hexane, Chloroform, Ethanol, Ethyl acetate and aqueous were evaluated against 4 bacterial strains viz. &lt;em&gt;E. coli&lt;/em&gt; (MTCC 40), &lt;em&gt;S. aureus&lt;/em&gt; (MTCC 87),&lt;em&gt; P. aeruginosa&lt;/em&gt; (MTCC 424), &lt;em&gt;B. subtilis&lt;/em&gt; (MTCC 121). &lt;strong&gt;Results:&lt;/strong&gt; The diagnostic characters were evaluated and documented. All the extracts showed good antimicrobial activity. &lt;strong&gt;Conclusion:&amp;nbsp;&lt;/strong&gt;Obtained standards will provide referential information for correct identification, purity, standardization and preparation of monograph. The work confirms that the studied plant has potent antimicrobial activity and has potential for antimicrobial drug. These results may constitute a basis for promising future applied research that could investigate the use of this plant as antimicrobial drug.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s56</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Mamta Arora&lt;sup&gt;1&lt;/sup&gt;, Gurjinder Kaur&lt;sup&gt;2&lt;/sup&gt;, Parvinderdeep S Kahlon&lt;sup&gt;3&lt;/sup&gt;, Anupama Mahajan&lt;sup&gt;4&lt;/sup&gt;, Jaspreet K Sembi&lt;sup&gt;5&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biotechnology, A.S.B.A.S.J.S.M. College, Bela Rupnagar, Punajb, INDIA, Research scholar of IK Gujral Punjab Technical University, Kapurthala, Punjab, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;St. Lawrence College (CANADA).&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Institute of Cellular and Molecular Botany, University of Bonn, Bonn, GERMANY.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biotechnology, SUS College of Engineering and Technology, Tangori, Mohali, Punjab, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Botany, Panjab University, Chandigarh, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mahendrakumar M</style></author><author><style face="normal" font="default" size="100%">Nirmalraj S</style></author><author><style face="normal" font="default" size="100%">Ravikumar M</style></author><author><style face="normal" font="default" size="100%">Bharath B</style></author><author><style face="normal" font="default" size="100%">Seeni S</style></author><author><style face="normal" font="default" size="100%">Perinbam K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic, Phytochemical and Physicochemical Investigations of Hypericum hookerianum Wight &amp; Arn. (Hypericaceae) of Palni Hills, India</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hypericum hookerianum</style></keyword><keyword><style  face="normal" font="default" size="100%">Palni Hills.</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognosy</style></keyword><keyword><style  face="normal" font="default" size="100%">Physiochemistry</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/171</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">750-756</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Hypericum hookerianum&lt;/em&gt; Wight and Arn. (Hooker&amp;rsquo;s wort) is a lesser known unfamiliar yet critically endangered native therapeutically active native medicinal plant. It is being characterized by the presence of various secretory glands. &lt;strong&gt;Methodology:&lt;/strong&gt; In this present study, characterization of the plant in terms of morphology, anatomy and histochemistry of tissues and phytochemicals and antimicrobial potentials were made. &lt;strong&gt;Results:&lt;/strong&gt; The epidermal layer contains oil cells while histochemistry showed the presence of the secondary metabolites. Qualitative analysis indicated presence of maximum phytocompounds in the high polar ethanolic extract; flavonoids, anthocyanin and phenol are prominently present and quantified. &lt;strong&gt;Conclusion:&lt;/strong&gt; The results suggest that the less studied herb, &lt;em&gt;H. hookerianum&lt;/em&gt; is a multifaceted high value species having a wide range of phytochemicals with abundant medicinal properties.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">750</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Mahendrakumar M&lt;sup&gt;1&lt;/sup&gt;, Nirmalraj S&lt;sup&gt;1&lt;/sup&gt;, Ravikumar M&lt;sup&gt;1&lt;/sup&gt;, Bharath B&lt;sup&gt;1&lt;/sup&gt;, Seeni S&lt;sup&gt;2&lt;/sup&gt;, Perinbam K&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;PG and Research Department of Plant Biology and Plant Biotechnology, Government Arts College for Men, (Autonomous), Nandanam, Chennai, Tamil Nadu, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;School of Biosciences, Mar Athanasios College for Advanced Studies (MACFAST), Tiruvalla, Kerala, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amna Parveen</style></author><author><style face="normal" font="default" size="100%">Zahra</style></author><author><style face="normal" font="default" size="100%">Muhammad Qudratullah Farooqi</style></author><author><style face="normal" font="default" size="100%">Whang Wan Kyunn</style></author><author><style face="normal" font="default" size="100%">Muhammad Arshad</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Screening and Content Determination of Different Species of Genus Caesalpinia belonging to Different Origin with Antidiabetic Activity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antidiabetic</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidants</style></keyword><keyword><style  face="normal" font="default" size="100%">Caesalpinia</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC Fingerprint</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical content.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/170</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">743-749</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aim:&lt;/strong&gt; The main aim of the study is to investigate the phytochemical screening of &lt;em&gt;C. decapetala&lt;/em&gt; along with the content determination of different species of genus &lt;em&gt;Caesalpinia&lt;/em&gt; with respect to their antidiabetic activity and identification of most bioactive species belonging to different origins. &lt;strong&gt;Methods:&lt;/strong&gt; To achieve our goal different species of genus &lt;em&gt;Caesalpinia&lt;/em&gt; collected from China and Pakistan were subjected to open column chromatography, High Pressure Liquid Chromatography (HPLC), antioxidant, and antidiabetic assays for evaluation. &lt;strong&gt;Results:&lt;/strong&gt; From &amp;eta;-BuOH fraction of &lt;em&gt;C. decapetala&lt;/em&gt; extract, eight compounds were isolated using open column chromatography and identified as apigenin-7-rhamnoside (1), 4-O-methylepisappanol (2), caesalpinol (3), daucosterol (4), astragalin (5), kaempferol (6), quercitrin (7), and naringin (8) using Nuclear Magnetic Resonance (NMR) spectroscopy. HPLC analysis of different species of genus &lt;em&gt;Caesalpinia&lt;/em&gt; showed that the most active antidiabetic compound &amp;lsquo;quercitrin&amp;rsquo; was present more in &lt;em&gt;C. pulcherrima&lt;/em&gt; followed by decreasing order in &lt;em&gt;C. sappan, C.decapetala,&lt;/em&gt; and &lt;em&gt;C. bonduc.&lt;/em&gt; &lt;strong&gt;Conclusion:&lt;/strong&gt; The results indicated that quercitrin is the most bioactive content and &lt;em&gt;C. pulcherrima&lt;/em&gt; is most bioactive specie of China origin from genus &lt;em&gt;Caesalpinia&lt;/em&gt;.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">743</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Amna Parveen&lt;sup&gt;1,2,3,*&lt;/sup&gt;, Zahra&lt;sup&gt;4&lt;/sup&gt;, Muhammad Qudratullah Farooqi&lt;sup&gt;5&lt;/sup&gt;, Whang Wan Kyunn&lt;sup&gt;2&lt;/sup&gt;, Muhammad Arshad&lt;sup&gt;4&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;College of Pharmacy, Gachon University, No. 191, Hambakmoero, Yeonsu-gu, Incheon 406-799, REPUBLIC OF KOREA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&amp;nbsp;&lt;/sup&gt;Pharmaceutical Resources Botany Laboratory, Department of Pharmacognosy, College of Pharmacy, Chung-Ang University, Room No:416, bldg.: 102, 221, Heukseok-dong, Dongjak gu, Seoul 156-756, REPUBLIC OF KOREA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacognosy, College of Pharmacy, Government College University Faisalabad, Faisalabad, PAKISTAN.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Institute of Environmental Sciences and Engineering, School of Civil and Environmental Engineering, National University of Sciences and Technology, Sector H-12, Islamabad 44000, PAKISTAN.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Applied Plant Sciences, College of Agriculture and Life Sciences, Kangwon National University, Chuncheon 24341, REPUBLIC OF KOREA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Muthukumaran Pakkirisamy</style></author><author><style face="normal" font="default" size="100%">Suresh Kumar Kalakandan</style></author><author><style face="normal" font="default" size="100%">Karthikeyen Ravichandran</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Screening, GC-MS, FT-IR Analysis of Methanolic Extract of Curcuma caesia Roxb (Black Turmeric)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Curcuma caesia Roxb</style></keyword><keyword><style  face="normal" font="default" size="100%">FT-IR</style></keyword><keyword><style  face="normal" font="default" size="100%">GC MS</style></keyword><keyword><style  face="normal" font="default" size="100%">Phyto chemical</style></keyword><keyword><style  face="normal" font="default" size="100%">α-Santalol and Retinal.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/202</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">952-956</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aims:&lt;/strong&gt; The purpose of the current study is to monitor the phytochemical constituents in the &lt;em&gt;Curcuma caesia&lt;/em&gt; Roxb.by GC MS and FT-IR analysis. &lt;strong&gt;Methods:&lt;/strong&gt; The Rhizomes of &lt;em&gt;Curcuma caesia&lt;/em&gt; Roxb was extracted with Methanol at room temperature for 8 h. The bioactive compounds of &lt;em&gt;Curcuma caesia&lt;/em&gt; Roxb have been evaluated using GC-MS and FT-IR. &lt;strong&gt;Results:&lt;/strong&gt; Preliminary phytochemical analysis revealed the presence of tannins, terpenoids, flavonoid, alkaloid, phenol, phytosterol Quinones and saponins. Totally 15 compounds were identified and the chromatograph showed peaks with individual compounds. The major constituents were identified in the Methanolic extract were &amp;alpha;-Santalol (46.90%), Retinal (10.72%), Ar-tumerone(10.38%), Alloaromadendrene (5.93%), Megastigma-3,7(E),9-triene (4.80%), Benzene, 1-(1,5-dimethyl- 4-hexenyl)-4-methyl(4.38%) , 5,8,11,14,17-Eicosapentaenoic acid, methyl ester, (all-Z)-(4.26%) Tricyclo[8.6.0.0(2,9)]hexadeca-3,15-diene, trans-2,9-anti-9,10-trans-1,10 (3.26%) and many other compounds were identified as low level. The FTIR analysis confirmed the presence of N-H , O-H , C=C , C-H, C-O and CH3 functional groups. &lt;strong&gt;Conclusion:&lt;/strong&gt; The result of this study offer a platform of using &lt;em&gt;Curcuma caesia&lt;/em&gt; Roxb as herbal alternative for various diseases and it can be used as functional and pharmaceutical food.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">952</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Muthukumaran Pakkirisamy, Suresh Kumar Kalakandan&lt;sup&gt;*&lt;/sup&gt; and Karthikeyen Ravichandran &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Food Safety and Quality Testing Laboratory, Indian Institute of Food Processing Technology.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pratik Kumar Chatterjee</style></author><author><style face="normal" font="default" size="100%">Vinodini Nithyananda Madom Anantharaya</style></author><author><style face="normal" font="default" size="100%">Rashmi Kaup Shiva</style></author><author><style face="normal" font="default" size="100%">Nayanatara Arun Kumar</style></author><author><style face="normal" font="default" size="100%">Sneha Bhoja Shetty</style></author><author><style face="normal" font="default" size="100%">Suman Veerappa Budihal</style></author><author><style face="normal" font="default" size="100%">Mangalore Ramesh Bhat</style></author><author><style face="normal" font="default" size="100%">Kunal</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pre and Post-Treatment Effects: Estimation of Serum Testosterone and Lipid Peroxidation Levels on Moringa olifera Extract Induced Cadmium Exposed Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cadmium</style></keyword><keyword><style  face="normal" font="default" size="100%">MDA</style></keyword><keyword><style  face="normal" font="default" size="100%">Morniga olifera extract.</style></keyword><keyword><style  face="normal" font="default" size="100%">Oxidative stress</style></keyword><keyword><style  face="normal" font="default" size="100%">Testosterone</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/185</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">846-849</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Cadmium (Cd), is a toxic metal which affects various organs including testis. It produces oxidative stress leading to male infertility. Moringa tree, is a natural plant with a great therapeutic value and hence it is found to be effective both in prevention and treatment of various conditions including reducing toxicity of hazardous materials. The aim of the present study was to examine the effects of Pre-and Post-treatment with &lt;em&gt;Moringa oliefera&lt;/em&gt; leaf extract (MoE) on testis in cadmium exposed rats. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The present study was conducted at the Department of Physiology, Kasturba Medical College (KMC), Mangalore, Manipal University (MU), Karnataka, India, between (2011-2013). This prospective study consisted a total of 30 rats. These were divided into 5 groups with group I being the control. Data were presented as mean &amp;plusmn;SD. student&amp;rsquo;s t test was used as statistical tool, &lt;em&gt;p&lt;/em&gt;&amp;lt;0.05 considered statistically significant. Group IV and V were pre-and post-MoE treated groups respectively. Serum testosterone and tissue lipid peroxidation levels were estimated.&lt;strong&gt; Results:&lt;/strong&gt; Treatment with MoE prior and after administration of cadmium, respectively showed an increase significantly in the testosterone levels and a decrease in the tissue lipid peroxidation as compared to the group treated with cadmium. However, the pre-treatment showed better results in combatting the toxic effects of cadmium. &lt;strong&gt;Conclusion:&lt;/strong&gt; This study shows that &lt;em&gt;Moringa olifera&lt;/em&gt; leaf extract altered the testosterone and tissue lipid peroxidation levels. Also, pre-treatment showed better outcome.&lt;/p&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; contenteditable=&quot;true&quot; aria-hidden=&quot;true&quot;&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;Background: Cadmium (Cd), is a toxic metal which affects various organs including testis.&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;It produces oxidative stress leading to male infertility. Moringa tree, is a natural plant with&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;a great therapeutic value and hence it is found to be effective both in prevention and treatment&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;of various conditions including reducing toxicity of hazardous materials. The aim of the&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;present study was to examine the effects of Pre-and Post-treatment with Moringa oliefera&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;leaf extract (MoE) on testis in cadmium exposed rats. Materials and Methods: The present&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;study was conducted at the Department of Physiology, Kasturba Medical College (KMC),&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;Mangalore, Manipal University (MU), Karnataka, India, between (2011-2013). This prospective&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;study consisted a total of 30 rats. These were divided into 5 groups with group I being&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;the control. Data were presented as mean &amp;plusmn;SD. student&amp;rsquo;s t test was used as statistical tool,&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;p&amp;lt;0.05 considered statistically significant. Group IV and V were pre-and post-MoE treated&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;groups respectively. Serum testosterone and tissue lipid peroxidation levels were estimated.&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;Results: Treatment with MoE prior and after administration of cadmium, respectively showed&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;an increase significantly in the testosterone levels and a decrease in the tissue lipid peroxidation&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;as compared to the group treated with cadmium. However, the pre-treatment showed&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;better results in combatting the toxic effects of cadmium. Conclusion: This study shows that&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;Moringa olifera leaf extract altered the testosterone and tissue lipid peroxidation levels. Also,&lt;/div&gt;
&lt;div class=&quot;ephox-sloth-bin ephox-sloth-bin_22207819311505710213931&quot; style=&quot;position: fixed; top: 0px; width: 100px; height: 100px; overflow: hidden; opacity: 0; left: -100000px;&quot; aria-hidden=&quot;true&quot;&gt;pre-treatment showed better outcome.&lt;/div&gt;
&lt;/div&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">846</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Pratik Kumar Chatterjee, Vinodini Nithyananda Madom Anantharaya, Rashmi Kaup Shiva, Nayanatara Arun Kumar, Sneha Bhoja Shetty, Suman Veerappa Budihal, Mangalore Ramesh Bhat, Kunal &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Department of Physiology, Kasturba Medical College (KMC), Mangalore-575004, Manipal University (MU), Karnataka, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ming Shin Neo</style></author><author><style face="normal" font="default" size="100%">Shraddha Manish Gupta</style></author><author><style face="normal" font="default" size="100%">Tahir Mehmood Khan</style></author><author><style face="normal" font="default" size="100%">Manish Gupta</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Quantification of Ethanol Content in Traditional Herbal Cough Syrups</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alcohol content</style></keyword><keyword><style  face="normal" font="default" size="100%">Enzymatic analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethanol concentration</style></keyword><keyword><style  face="normal" font="default" size="100%">Herbal cough medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Herbal preparation</style></keyword><keyword><style  face="normal" font="default" size="100%">Quantitative analysis.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/181</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">821-827</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The use of alcohol as an excipient in pharmaceutical preparations raises safety concerns, especially when used in high concentration. This study aims to scrutinize the ethanol concentration in traditional herbal cough syrups available over-the-counter (OTC) in Malaysia. &lt;strong&gt;Method:&lt;/strong&gt; Enzymatic analysis was adopted to estimate the alcohol contents of five selected syrups. The principle reaction involved ethanol oxidation by nicotinamide-adenine dinucleotide (NAD) in the presence of the enzyme alcohol dehydrogenase (ADH), forming acetaldehyde, reduced NAD (NADH) and a proton. The ethanol concentration of each syrup was quantitatively determined by detecting NADH using UV spectrophotometry at detection wavelength of 340 nm. &lt;strong&gt;Results:&lt;/strong&gt; The ethanol percentage by volume (% v/v) in the tested syrups ranges from 0.102% to 2.576%. All five syrups studied comply with the FDA requirement for drugs for adults and children &amp;gt;6 years since they do not contain more than 5% ethanol. However, three syrups do not fulfil the requirement for use in children &amp;lt;6 years as they contain higher than 0.5% ethanol, yet they are inappropriately indicated on their packaging for use in children &amp;gt;3 years. In terms of safety, all studied syrups fulfil European Medicine Agency&amp;rsquo;s (EMA) recommendation as they will not induce a blood alcohol concentration (BAC) higher than 0.125g/L after a single dose. Nevertheless, none of these syrups comply with Malaysian Drug Registration Guidance on labelling requirements as they do not disclose their alcohol contents on the packaging. &lt;strong&gt;Conclusion:&lt;/strong&gt; More rigorous regulation on alcohol content in herbal preparations, and disclosure of alcohol content in product packagings should be enforced.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">821</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ming Shin Neo&lt;sup&gt;1&lt;/sup&gt;, Shraddha Manish Gupta&lt;sup&gt;1&lt;/sup&gt;,&lt;sup&gt;2&lt;/sup&gt;, Tahir Mehmood Khan&lt;sup&gt;1&lt;/sup&gt;, Manish Gupta&lt;sup&gt;1*&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;School of Pharmacy, Monash University Malaysia, Selangor, MALAYSIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Gurukrupa Institute of Pharmacy, NH 222, Near Chhatrapati Sugar Factory, Malipargaon Phata , Majalgoan, Beed 431131, Maharashtra, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Venkata Siva Satyanarayana Kantamreddi</style></author><author><style face="normal" font="default" size="100%">V. Thirumala Veni</style></author><author><style face="normal" font="default" size="100%">G. Y. S. K. Swamy</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Quantitative Approach to Estimate both Essential and Non-essential Elements in Some Commercial Samples of Triphala churna by using WD-XRF Spectrometry</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ayurveda</style></keyword><keyword><style  face="normal" font="default" size="100%">Elemental analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">ICP-MS</style></keyword><keyword><style  face="normal" font="default" size="100%">ISM</style></keyword><keyword><style  face="normal" font="default" size="100%">Triphala churna</style></keyword><keyword><style  face="normal" font="default" size="100%">WD-XRF</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">April 2017 </style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-3/10.5530pj.2017.3.64</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">378-381</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The need for quality control of herbal drugs is in demand in order to ensure the purity, safety and efficacy of herbal products. A total of 19 elements including essential and non-essential elements were characterized in five commercial samples of &lt;em&gt;Triphala churna&lt;/em&gt; using WD-XRF spectrometry. &lt;strong&gt;Method:&lt;/strong&gt; The WD-XRF method was validated for each element by a pre-calibrated program using five Chinese certified reference materials of vegetable standards (NCS ZC73012, NCS ZC73013, NCS ZC73017, NCS ZC85006 and NCS DC73348). &lt;strong&gt;Results:&lt;/strong&gt; The following elements were detected in all the samples out of 19 elements tested with increasing order of concentrations (mg/kg): Cr (3) &amp;lt; Cu (7) &amp;lt; Ba (24) &amp;lt; Zn (31) &amp;lt; Pb (46) &amp;lt; Mn (57) &amp;lt; S (700) &amp;lt; Na (1064) &amp;lt; Mg (1250) &amp;lt; Fe (1329) &amp;lt; P (1400) &amp;lt; Cl (2960) &amp;lt; Ca (3110) &amp;lt; Si (4350) &amp;lt; K (15130). Lead (41-46 mg/kg), a nonessential element was found above its PDE limit (&amp;le; 10 mg/kg). &lt;strong&gt;Conclusion:&lt;/strong&gt; WD-XRF method was found simple, rapid, reliable and non-destructive technique to investigate the elemental concentrations in herbal drugs.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">378</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Venkata Siva Satyanarayana Kantamreddi&lt;sup&gt;1*&lt;/sup&gt;, V. Thirumala Veni&lt;sup&gt;1&lt;/sup&gt; and G. Y. S. K. Swamy&lt;sup&gt;2 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Centre for Chemical Analysis, Central Research Laboratory, GIT, GITAM University, Visakhapatnam, Andhra Pradesh, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Laboratory of X-ray Crystallography, Indian Institute of Chemical Technology, CSIR, Hyderabad, Telangana, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tom Mathew Kalappurayil</style></author><author><style face="normal" font="default" size="100%">Benny Pulinilkkumthadathil Joseph</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Review of Pharmacognostical Studies on Moringa oleifera Lam. flowers</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Bioactivity</style></keyword><keyword><style  face="normal" font="default" size="100%">Bioassay</style></keyword><keyword><style  face="normal" font="default" size="100%">Extracts</style></keyword><keyword><style  face="normal" font="default" size="100%">Flower</style></keyword><keyword><style  face="normal" font="default" size="100%">GCMS</style></keyword><keyword><style  face="normal" font="default" size="100%">Moringa</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword><keyword><style  face="normal" font="default" size="100%">Therapeutic</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2016</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-3/10.5530pj.2017.1.1</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">1-7</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;em&gt;Moringa oleifera&lt;/em&gt; Lam. of the family Moringaceae, popularly called &amp;lsquo;miracle tree&amp;rsquo; is a native of sub Himalayan tracts of Northern India and is widely cultivated in tropical and subtropical regions. Research on Moringa mainly pivoted around its leaves and seeds because of their immense nutraceutical potential but recently there is a greater interest in flowers too, mostly inspired by the positive outcomes of several pharmacognostical studies on flowers. Moringa flower is a rich reservoir of bioactive phytochemicals and crude flower extracts showed promising antibacterial, antifungal, anti larval, antioxidant, anti inflammatory and anticancer properties. This review concisely presents the various phytochemicals identified and isolated as well as the various bioassays employed to validate the therapeutic potential of flower. It is prepared after a detailed search on Google scholar. Reports on &lt;em&gt;Moringa oleifera&lt;/em&gt; flower were sorted and tabulated based on the bioassays performed and solvents used for extraction. A grading pattern is adopted for comparing efficiency of different extracts in eliciting bioactivities. Many of these studies are at the preliminary stage but two of them present advanced mechanisms. First is the presence of a proteinaceous larvicidal compound &amp;lsquo;MoFTI&amp;rsquo; in the flower capable of inhibiting larval trypsin of &lt;em&gt;Aedes aegypti&lt;/em&gt;. The second describes flower extract&amp;rsquo;s anti inflammatory mechanism effecting via NF-KB pathway and consequent suppression of inflammatory mediators&amp;rsquo; activation, but short of identifying lead compound/compounds behind this effect. Thus authors suggest further studies to elucidate the detailed mechanisms, identify and isolate the active compound or compounds of synergism behind the many therapeutic potential of the Moringa flower extracts.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">1</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Tom Mathew Kalappurayil&lt;sup&gt;*&lt;/sup&gt;, Benny Pulinilkkumthadathil Joseph&lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Zoology, St Thomas College, Pala PIN 686574, Kottayam district, Kerala, INDIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arshad Husain Rahmani</style></author><author><style face="normal" font="default" size="100%">Amjad Ali Khan</style></author><author><style face="normal" font="default" size="100%">Yousef Homood Aldebasi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Saffron (Crocus sativus) and its Active Ingredients: Role in the Prevention and Treatment of Disease</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-tumour activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Crocus sativus</style></keyword><keyword><style  face="normal" font="default" size="100%">Toxicity level.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/190</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">873-879</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Crocus sativus&lt;/em&gt; is a member of iridaceae family and its use in health management is in practice since ancient time. Additionally, research based on clinical trials and animal models have advocates its role in disease cure without any severe adverse complications. The aim of this study is to summarize the study of saffron and its ingredients based on &lt;em&gt;in vivo&lt;/em&gt; and &lt;em&gt;in vitro&lt;/em&gt; and role in disease cure and prevention. &lt;strong&gt;Materials:&lt;/strong&gt; This study was designed through the search engines such as Pub Med, Scopus and Google Scholar. The keywords used for the search were mainly focused on Saffron with health benefit and its therapeutics role in different diseases. &lt;strong&gt;Result:&lt;/strong&gt; Saffron stigma is mixture of various components and recent studies have proven that saffron and its active ingredients play a key role in disease management. Moreover, clinical trials based study on the use of saffron and its individual components have confirmed the health promising effects. &lt;strong&gt;Conclusion:&lt;/strong&gt; Although Saffron has potential role in the disease cure and prevention via modulation of anti-oxidant, anti-inflammatory, anti-tumour, anti-microbial and anti-diabetic activity. Furthermore, advanced research is needed to elaborate the role of saffron in health management and its mechanism of action in the modulation of biological activities.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">873</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Arshad Husain Rahmani&lt;sup&gt;1*&lt;/sup&gt;, Amjad Ali Khan &lt;sup&gt;2&lt;/sup&gt;, Yousef Homood Aldebasi&lt;sup&gt;3&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, SAUDI ARABIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Basic Health Science, College of Applied Medical Sciences, Qassim University, SAUDI ARABIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Optometry, College of Applied Medical Sciences, Qassim University, SAUDI ARABIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Cennet Ragbetli</style></author><author><style face="normal" font="default" size="100%">Semiha Dede</style></author><author><style face="normal" font="default" size="100%">Feride Koc</style></author><author><style face="normal" font="default" size="100%">Veysel Yuksek</style></author><author><style face="normal" font="default" size="100%">Murat Cetin Ragbetli</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The Serum Protein Fractions in Streptozotocin (STZ) Administrated Rat Models</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">electrophoresis</style></keyword><keyword><style  face="normal" font="default" size="100%">experimental diabetes</style></keyword><keyword><style  face="normal" font="default" size="100%">Rat</style></keyword><keyword><style  face="normal" font="default" size="100%">serum proteins</style></keyword><keyword><style  face="normal" font="default" size="100%">STZ</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">35-38</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Experimental diabetes can be induced using chemical agents such as streptozotocin. &lt;strong&gt;Objective:&lt;/strong&gt; This study aimed to investigate the effect of streptozotocin (STZ) which is most important agent to produce experimental diabetic model at two different doses on serum protein fractions in rat models. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Twenty-four male rats that weighed an average of 250 g and were 3&amp;ndash;4 months old were used as the experimental models. They were sorted into three groups composed of eight rats each of STZ 55 mg/kg, STZ 65 mg/kg and control. Diabetes was induced by administering STZ 55 mg/kg and 65 mg/kg intraperitoneally. The serum protein fractions were analyzed by cellulose acetate electrophoresis. &lt;strong&gt;Results:&lt;/strong&gt; No significant difference was observed between the groups for all fractions except alpha-2 and beta globulins. The alpha-2 and beta globulin levels were significantly higher in the 55 mg/kg group than in the 65 mg/kg STZ and control groups (p&amp;lt;0.05). &lt;strong&gt;Conclusion:&lt;/strong&gt; This increase may be due to the involvement of different proteins in the alpha-2 and beta globulin protein fractions.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">35</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Cennet Ragbetli&lt;sup&gt;1&lt;/sup&gt;, Semiha Dede&lt;sup&gt;2&lt;/sup&gt;*, Feride Koc&lt;sup&gt;3&lt;/sup&gt;, Veysel Yuksek&lt;sup&gt;4&lt;/sup&gt;, Murat Cetin Ragbetli&lt;sup&gt;5&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Microbiology, Medicine Faculty, Veterinary Medicine School, Van, 65080 TURKEY.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biochemistry, Veterinary Medicine Faculty, Veterinary Medicine School, Van, 65080 TURKEY.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department Pharmacology and Toxicology, Veterinary Faculty Erciyes University, Veterinary Medicine School, Biochemistry Department, Van, 65080 Turkey.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Ozalp Vocational High School, YuzuncuYil University, Veterinary Medicine School, Van, 65080 TURKEY.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Histology and Embryology, Medicine Faculty, Veterinary Medicine School, Biochemistry Department, Van, 65080 TURKEY.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ankita Misra</style></author><author><style face="normal" font="default" size="100%">Pushpendra Kumar Shukla</style></author><author><style face="normal" font="default" size="100%">Bhanu Kumar</style></author><author><style face="normal" font="default" size="100%">Abhishek Niranjan</style></author><author><style face="normal" font="default" size="100%">AKS Rawat</style></author><author><style face="normal" font="default" size="100%">Sharad Srivastava</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Simultaneous-HPLC Quantification of Phenolic Acids in Traditionally used Ayurvedic Herb Diplocyclos palmatus (L.) Jeffry</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti diabetic</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti oxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Diplocyclos palmatus</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolic acid</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">/files/PJ-9-4/10.5530pj.2017.4.78</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">483-487</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt;The present study deals with the simultaneous HPLC-quantification of phenolic acid(s) in the aerial parts of &lt;em&gt;Diplocyclos palmatus &lt;/em&gt;(Cucurbitaceae) and evaluation of their bioactivity potential through &lt;em&gt;in vitro &lt;/em&gt;antioxidant assay&amp;rsquo;s. &lt;strong&gt;Method:&lt;/strong&gt; The HPLC elution was done using C&lt;sub&gt;18&lt;/sub&gt; column using gradient (binary phases) solvent system at a flow rate of 0.6 ml/min. Total phenolic and, flavonoid contents were determined and the antioxidant potential was estimated by four assay&amp;rsquo;s viz. DPPH radical scavenging assay, ferric reducing power assay, total antioxidant capacity and 2-deoxy ribose assay. &lt;strong&gt;Results:&lt;/strong&gt; The species is rich in three phenolic acids, among which gallic acid (1708 ug/g) is in maximum concentration followed by caeffic acid (437 ug/g) and protocateuchic acid (337.7 ug/g). Total phenolic content was higher (10.5 mg/g) than flavonoid content (3.78 mg/g) and TAC was found at 0.137 mg/g ASE (ascorbic acid equivalent). IC&lt;sub&gt;50&lt;/sub&gt; of &lt;em&gt;D. palmatus &lt;/em&gt;extract for scavenging of hydroxyl radical by 2-deoxy ribose and DPPH was at concentration of 125.61 &amp;plusmn; 0.834 (&amp;mu;g/ml) and 353.71 &amp;plusmn; 0.663 (&amp;mu;g/ml) respectively. &lt;em&gt;In vitro &lt;/em&gt;antidiabetiv potential, via inhibition of alpha amylase enzyme through starch iodine and 3,5- DNS assay reveals the IC&lt;sub&gt;50&lt;/sub&gt; of extract at 146.31 &amp;plusmn; 0.415 ug/ml and 286.23 &amp;plusmn; 0.671 ug/ ml respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt;&amp;nbsp;The species (aerial part) was rich in phenolic acid with potential bioactivity, identified leads will be useful&amp;nbsp;in further chemical characterization and pharmacological validation.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><section><style face="normal" font="default" size="100%">483</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ankita Misra, Pushpendra Kumar Shukla, Bhanu Kumar, Abhishek Niranjan, AKS Rawat and Sharad Srivastava&lt;sup&gt;* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;em&gt;Pharmacognosy and Ethnopharmacology Division, CSIR-National Botanical Research Institute Lucknow (U.P.) 226001, INDIA.&lt;/em&gt;&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gopichand</style></author><author><style face="normal" font="default" size="100%">RL Meena</style></author><author><style face="normal" font="default" size="100%">P Kaur</style></author><author><style face="normal" font="default" size="100%">RD Singh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Standardization of Agrotechniques and Biochemical Assessment of Crataegus oxyacantha in Western Himalaya</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Bioactive compounds</style></keyword><keyword><style  face="normal" font="default" size="100%">Crataegus oxyacantha</style></keyword><keyword><style  face="normal" font="default" size="100%">FYM</style></keyword><keyword><style  face="normal" font="default" size="100%">Hormones</style></keyword><keyword><style  face="normal" font="default" size="100%">Spacing</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/385</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s69-s76</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;em&gt;C. oxyacantha&lt;/em&gt; is a high valued medicinal plant of Rosacea family. It is used to cure cardiac disorder in ayurvedic medicines. A field experiment was laid out in 2004 in CSIR-IHBT farm, by using different quantity of FYM and various spacing. Low growth in plant height was observed in first five years with higher dose of FYM, but in 2015 the significant height growth was recorded. From 2008 to 2015 all types of FYM applications produced statistically significant yield of seed production except in 2012 and 2014. The 22.50t/ha was the most statistically significant dose of FYM in relation to seed yield. The spacing did not produce any significant results for seed production. A vegetative propagation trial of &lt;em&gt;C. oxyacantha &lt;/em&gt;was also laid out using semi hard stem cuttings and some selected hormones (IAA, IBA, GA3 and Abscisic acid) with different concentrations. Statistically significant shoot sprouting (78.35%) was recorded when IBA of 1000 mg/L was used followed by 67.74% in case of 1500 mg/L of the same hormone. While lowest shoot sprouting (27.85%) was observed using 2000 mg/L of Abscisic acid. A statistically significant 5.67 cm and 5.33 cm shoot lengths were observed using 2000 mg/L of IAA and 1000 mg/L of IBA, respectively. In the case of shoot tillers 3.33 was recorded in 1500 mg/l. of IAA. Two new compounds and 9 known compounds were isolated from fruit extract.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">s69</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Gopichand&lt;sup&gt;1&lt;/sup&gt;*, RL Meena&lt;sup&gt;1&lt;/sup&gt;, P Kaur&lt;sup&gt;2&lt;/sup&gt;, RD Singh&lt;sup&gt;1 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of High Altitude Biology, CSIR - Institute of Himalayan Bioresource Technology, Palampur (H.P.) 176061 INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Sri Guru Gobind Singh College, Sector-26, Chandigarh-160019, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pawan Kumar Verma</style></author><author><style face="normal" font="default" size="100%">Rajinder Raina</style></author><author><style face="normal" font="default" size="100%">Mudasir Sultana</style></author><author><style face="normal" font="default" size="100%">Maninder Singh</style></author><author><style face="normal" font="default" size="100%">Pawan Kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Acetaminophen Induced Oxidative and Histopathological Alterations in Hepatic Tissue: Protective Effects of Alstonia Scholaris Leaf Extracts</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acetaminophen</style></keyword><keyword><style  face="normal" font="default" size="100%">Alstonia scholaris</style></keyword><keyword><style  face="normal" font="default" size="100%">Malondialdehyde.</style></keyword><keyword><style  face="normal" font="default" size="100%">Super oxide dismutase</style></keyword><keyword><style  face="normal" font="default" size="100%">Total antioxidant status</style></keyword><keyword><style  face="normal" font="default" size="100%">Total thiols</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June/2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">385-391</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Alstonia scholaris&lt;/em&gt; Linn. is the common ingredients of various herbal formulation. &lt;strong&gt;Objectives:&lt;/strong&gt; Present study was aimed to evaluate the oxidative and histopathological alterations in acetaminophen (APAP) induced hepatotoxicity and protective mechanisms of different leaf extracts of &lt;em&gt;A. scholaris&lt;/em&gt;. &lt;strong&gt;Methods:&lt;/strong&gt; Forty two wistar rats were randomly divided into seven groups with six rats in each and subjected to different treatments. Alterations in total oxidant status (TOS), total antioxidant status (TAS), oxidative stress index (OSI), total thiols (TTH), catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione-s-transferase (GST), malondialdehyde (MDA) levels and histopathological alterations in hepatic tissue were analyzed to assess the extent of hepatic damage induced by APAP and the protection imparted against it by aqueous or ethanolic leaf extract of &lt;em&gt;A. scholaris&lt;/em&gt;. &lt;strong&gt;Results:&lt;/strong&gt; Single high oral dose of APAP administration increased (p&amp;lt;0.05) hepatic levels of TOS, OSI and MDA and reduced TAS, TTH, SOD, CAT, GPx and GST activities indicating alteration in antioxidant system of hepatic tissue. The histopathological studies showed severe hepatic degeneration, vacuolization and granulation in cytoplasm, fragmentation of nuclei and membranes and infiltration of mononuclear cells on APAP treatment. Pre and post-treatments of aqueous or ethanolic extract following APAP administration restored TTH, reduced MDA and TOS and increased TAS compared to APAP treatment alone. &lt;strong&gt;Conclusions: &lt;/strong&gt;Observations of histopathological and antioxidant parameters indicates that restoration of TAS and TTH levels by leaf extracts may be the primary protective mechanism in APAP induced hepatotoxicity. Further treatments with ethanolic extract showed more hepatoprotective potential than the aqueous extract of &lt;em&gt;A. scholaris&lt;/em&gt;.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">385</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Pawan Kumar Verma&lt;sup&gt;1*&lt;/sup&gt;, Rajinder Raina&lt;sup&gt;1&lt;/sup&gt;, Mudasir Sultana&lt;sup&gt;1&lt;/sup&gt;, Maninder Singh&lt;sup&gt;2&lt;/sup&gt;, Pawan Kumar&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Division of Veterinary Pharmacology and Toxicology, Faculty of Veterinary Sciences and Animal Husbandry, R S Pura, Jammu, 181102, Jammu &amp;amp; Kashmir, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Division of Veterinary Public Health and Epidemiology, Faculty of Veterinary Sciences and Animal Husbandry, R S Pura, Jammu, 181102, Jammu &amp;amp; Kashmir, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Division of Pathology, Indian Veterinary Research Institute, Izatnagar, Bareilly, UP. 243122, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tanuja Singh</style></author><author><style face="normal" font="default" size="100%">Ruchi</style></author><author><style face="normal" font="default" size="100%">Anjali singh</style></author><author><style face="normal" font="default" size="100%">Ravish Kumar</style></author><author><style face="normal" font="default" size="100%">Jitendra Kumar Singh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Acute toxicity study of Phyllanthus niruri and its effect on the cyto-architectural structure of nephrocytes in Swiss albino mice Mus-musculus</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biochemical</style></keyword><keyword><style  face="normal" font="default" size="100%">Histological analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Kidney</style></keyword><keyword><style  face="normal" font="default" size="100%">LD50</style></keyword><keyword><style  face="normal" font="default" size="100%">P. niruri.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">09/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">77-80</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; In the era of herbal renaissance, world is moving towards the medicinal plant that repairs and strengthening the body system without any toxic side effects. Popular medicinal plant &lt;em&gt;Phyllanthus niruri&lt;/em&gt; contains various bioactive molecules, the present study aimed to observe the biochemical and cyto-architectural alterations in kidney associated with acute oral toxicity (LD&lt;sub&gt;50&lt;/sub&gt;) of aqueous extract of &lt;em&gt;P.niruri&lt;/em&gt; in Swiss albino mice. However, limited data is available about the toxicity of herbal remedies used for medication, which is a critical constrain. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; For the acute oral toxicity study, the animals were divided into six groups of 6 mice each. Group&amp;ndash;I was named control group and the treatment groups were administered aqueous leaf extract of &lt;em&gt;P.niruri&lt;/em&gt; orally at different doses of 500 mg/Kg bw (Group-II), 1000 mg/Kg bw (Group-III), 2000 mg/Kg bw (Group-IV), 2500 mg/Kg bw (Group-V) and 3000 mg/Kg bw (Group-VI) for 15 consecutive days. The mice were sacrificed on and serum was collected for the biochemical analysis. The kidney was dissected and processed for histological analysis. &lt;strong&gt;Results:&lt;/strong&gt; The LD&lt;sub&gt;50&lt;/sub&gt; dose of &lt;em&gt;P.niruri &lt;/em&gt;was found to be 2590.984 mg/Kg bw in Swiss albino mice model in laboratory condition. The result showed the elevated serum level of urea in treated group of mice at higher doses which was found to be statistically significant as compared to the control (Group&amp;ndash;I). There were no any significant increase in serum creatinine has been observed. Histological alteration were observed at higher dose more than 2500 mg/Kg bw (Group-VI). &lt;strong&gt;Conclusion:&lt;/strong&gt; It is evident from our study that &lt;em&gt;P. niruri &lt;/em&gt;may have toxic effect at high doses. Therefore, it should be ingested with precautions.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">77</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Tanuja Singh&lt;sup&gt;1&lt;/sup&gt;, Ruchi&lt;sup&gt;2&lt;/sup&gt;, Anjali Singh&lt;sup&gt;3&lt;/sup&gt;, Ravish Kumar&lt;sup&gt;3&lt;/sup&gt; and Jitendra Kumar Singh&lt;sup&gt;4&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Botany, Thakur Prasad Singh, College, Magadh University, Patna.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Botany, Braj Mohan Das College, Dayalpur, Babasaheb Bhimrao Ambedkar, Bihar University, Bihar, India&amp;ndash;844502.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Research Centre, Mahavir Cancer Sansthan, Phulwarisharif, Patna, India.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Research, S.S. Hospital and Research Institute, Patna, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Toru Konishi</style></author><author><style face="normal" font="default" size="100%">Masaaki Minami</style></author><author><style face="normal" font="default" size="100%">Zhixia Jiang</style></author><author><style face="normal" font="default" size="100%">Tetsuya Arai</style></author><author><style face="normal" font="default" size="100%">Toshiaki Makino</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antibacterial activity of Shin'iseihaito (Xin Yi Qing Fei Tang) against Streptococcus pneumoniae</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Baicalin</style></keyword><keyword><style  face="normal" font="default" size="100%">Scutellaria baicalensis</style></keyword><keyword><style  face="normal" font="default" size="100%">Shin'iseihaito</style></keyword><keyword><style  face="normal" font="default" size="100%">Sinusitis</style></keyword><keyword><style  face="normal" font="default" size="100%">Streptococcus pneumoniae.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">09/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">20-23</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective: &lt;/strong&gt;Shin&amp;#39;iseihaito (Xin yi qing fei tang in Chinese, SSHT), a formula in traditional Japanese Kampo medicine and Chinese medicine comprising nine crude drugs, Gypsum, Ophiopogon Tuber, Scutellaria Root (SR, root of &lt;em&gt;Scutellaria baicalensis&lt;/em&gt;), &lt;em&gt;Gardenia Fruit&lt;/em&gt;, Anemarrhena Rhizome, Lilium Bulb, Magnolia Flower, Loquat Leaf, and Cimicifuga Rhizome, is commonly used to treat sinusitis associated with purulent nasal discharge and reddish nasal mucosa. We evaluated anti-bacterial activity of SSHT extract on &lt;em&gt;Streptococcus pneumoniae&lt;/em&gt;, the major cause of bacterial sinusitis. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Sterile paper disks impregnated with SSHT extract or each extract of its component were placed on sheep blood agar plates inoculated with &lt;em&gt;Streptococcus pneumoniae &lt;/em&gt;(ATCC 49619). The diameter of inhibitory zone was measured after 20-24 h incubation.&lt;strong&gt; Results: &lt;/strong&gt;SSHT extract and each water extract of Ophiopogon Tuber, SR, &lt;em&gt;Gardenia Fruit&lt;/em&gt;, Anemarrhena Rhizome, Lilium Bulb, Magnolia Flower, and Cimicifuga Rhizome showed significant antibacterial activity against &lt;em&gt;Streptococcus&lt;/em&gt;&lt;em&gt; pneumoniae&lt;/em&gt;, and SR extract exhibited the largest inhibitory zone. SR extract was partitioned into AcOEt, BuOH, and water layer, and water layer was further separated into 80% EtOH soluble and insoluble fraction. Among them, only 80% EtOH soluble fraction was exhibited antibacterial activity. In this fraction, we found baicalin as the major compounds, and baicalin exhibited antibacterial activity against &lt;em&gt;Streptococcus&lt;/em&gt;&lt;em&gt; pneumoniae &lt;/em&gt;in concentration-dependent manner. &amp;nbsp;&lt;strong&gt;Conclusion:&lt;/strong&gt; SSHT has antibacterial activity against &lt;em&gt;Streptococcus&lt;/em&gt;&lt;em&gt; pneumoniae&lt;/em&gt;, and SR and its major constituent baicalin contribute to the antibacterial activity of SSHT against &lt;em&gt;Streptococcus pneumoniae.&lt;/em&gt;&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">20</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Toru Konishi&lt;sup&gt;1&lt;/sup&gt;, Masaaki Minami&lt;sup&gt;2&lt;/sup&gt;, Zhixia Jiang&lt;sup&gt;3&lt;/sup&gt;, Tetsuya Arai&lt;sup&gt;3&lt;/sup&gt; and Toshiaki Makino&lt;sup&gt;1*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-dori, Mizuho-ku, Nagoya 467-8603, Japan.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Bacteriology, Graduate School of Medical Sciences, Nagoya City University,1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Research and Development Center, Kobayashi Pharmaceutiucal Co. Ltd., 4-10 Doshomachi 4-chome, Chuo-ku, Osaka, Japan.&lt;/p&gt;

&lt;p&gt;&amp;nbsp;&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sayeli Vinaykumar</style></author><author><style face="normal" font="default" size="100%">Urval Pundarik Rathnakar</style></author><author><style face="normal" font="default" size="100%">Ullal Sheetal Dinkar</style></author><author><style face="normal" font="default" size="100%">Kamath Priyanka</style></author><author><style face="normal" font="default" size="100%">Tiwary Gaurav</style></author><author><style face="normal" font="default" size="100%">Shenoy Ashok Kudgi</style></author><author><style face="normal" font="default" size="100%">Revappala Sekhar Nishith</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anti-inflammatory activity of BCM-95 (bio-enhanced formulation of turmeric with increased bioavailabilty) compared to Curcumin in Wistar rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-Inflammatory agents</style></keyword><keyword><style  face="normal" font="default" size="100%">Bioavailability</style></keyword><keyword><style  face="normal" font="default" size="100%">Curcumin</style></keyword><keyword><style  face="normal" font="default" size="100%">Inflammation</style></keyword><keyword><style  face="normal" font="default" size="100%">Wistar rats.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June/2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">380-384</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Objective&lt;/strong&gt;: To evaluate anti-inflammatory activity of bioenhanced turmeric formulation (BCM-95) compared to commercial Curcumin formulation (Curcuminoids 95%) in Carrageenan-induced acute inflammatory model. &lt;strong&gt;Materials and Methods&lt;/strong&gt;: Thirty six Wistar rats were divided into six groups-Normal control (2 ml of vehicle), Standard control (Indomethacin 10 mg/kg), 2 doses of BCM 95 (10 and 20 mg/kg) and Curcuminoids 95% (10 and 20 mg/kg). Paw volume was measured using a digital plethysmometer. Vehicle or test drugs were given to rats 30 min before carrageenan administration. Baseline paw volume reading (V&lt;sub&gt;0&lt;/sub&gt;) was noted just prior to administration of 0.1 ml of 1% carrageenan to right hind paw of the rat. Test paw volume readings (V&lt;sub&gt;t&lt;/sub&gt;) were measured at 30, 60, 120, 180, 240, 300 and 360 min, after carrageenan injection. Oedema expressed as increased paw volume (v&lt;sub&gt;t&lt;/sub&gt;-v&lt;sub&gt;0&lt;/sub&gt;) was noted and percentage inhibition of oedema was calculated for all treatment groups. &lt;strong&gt;Statistical analysis&lt;/strong&gt;: Difference between groups were analyzed with ANOVA followed by Tukey test. &lt;strong&gt;Results:&lt;/strong&gt; All treatment groups demonstrated significant (p&amp;lt;0.05) anti-inflammatory activity (oedema suppression) compared to normal control&lt;strong&gt;. &lt;/strong&gt;Anti-inflammatory activity of BCM 95 treated groups were comparable to standard control group except at certain time points, whereas the same activity at all-time points with Curcuminoid 95% treated groups were significantly less than standard control group. Percentage inhibition of paw oedema was maximum with standard control group followed by BCM 95 treated groups followed by Curcuminoid 95% treated groups. &lt;strong&gt;Conclusion:&lt;/strong&gt; BCM 95 treated groups showed significant anti-inflammatory activity compared to Curcuminoid 95% treated groups.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">380</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Sayeli Vinaykumar&lt;sup&gt;1&lt;/sup&gt;, Urval Pundarik Rathnakar&lt;sup&gt;2&lt;/sup&gt;, Ullal Sheetal Dinkar&lt;sup&gt;1&lt;/sup&gt;*, Kamath Priyanka&lt;sup&gt;1&lt;/sup&gt;, Tiwary Gaurav&lt;sup&gt;1&lt;/sup&gt;, Ashok Shenoy Kudgi&lt;sup&gt;1&lt;/sup&gt;, Revappala Sekhar Nishith&lt;sup&gt;3&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Kasturba Medical College, Mangaluru, Manipal University, Manipal, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology, Kanachur Institute of Medical Sciences, Deralakatte, Mangaluru. 575018, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Scoop Med Inc, Bengaluru, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sachin Kumar</style></author><author><style face="normal" font="default" size="100%">Ramesh B. Bodla</style></author><author><style face="normal" font="default" size="100%">Himangini Bansal</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antioxidant Activity of Leaf Extract of Aegle marmelos Correa ex Roxb.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Aegle marmelos</style></keyword><keyword><style  face="normal" font="default" size="100%">Cation scavenging</style></keyword><keyword><style  face="normal" font="default" size="100%">Free radical scavenging</style></keyword><keyword><style  face="normal" font="default" size="100%">Reducing power.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Oct 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">447-450</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Leaf extracts of &lt;em&gt;Aegle marmelos&lt;/em&gt; are reported to have hypoglycemic and anticancer effects. While a lot of information is available about the antioxidant activity of fruit of&lt;em&gt; A. marmelos&lt;/em&gt; not much information is available about the antioxidant activity of the leaf of&lt;em&gt; A. marmelos&lt;/em&gt;. &lt;strong&gt;Objective: &lt;/strong&gt;The primary objective if this study was to ascertain the antioxidant activity of leaf extract of &lt;em&gt;A. marmelos&lt;/em&gt; (AME). &lt;strong&gt;Methods:&lt;/strong&gt; AME was evaluated for total phenolic content (TPC) and total flavonoid content (TFC) by Folin-Ciocalteau reagent method and by aluminium chloride method, respectively. Antioxidant activity of AME was assessed by FRAP assay, DPPH assay, ABTS cation scavenging activity and by reducing power determination. &lt;strong&gt;Results&lt;/strong&gt;: High levels of TPC and TFC were found in AME which showed antioxidant activity comparable to vitamin C. Significant correlation between TPC, TFC and antioxidant activity of AME was found when Pearson&amp;rsquo;s correlation is applied. &lt;strong&gt;Conclusion:&lt;/strong&gt; This study proved that the leaves of&lt;em&gt; A. marmelos&lt;/em&gt; have high antioxidant component.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">447</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Sachin Kumar&lt;sup&gt;1*&lt;/sup&gt;, Ramesh B. Bodla&lt;sup&gt;2&lt;/sup&gt;, Himangini Bansal&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, DIPSAR, New Delhi, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmaceutical Chemistry, DIPSAR, New Delhi, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aditi Gupta</style></author><author><style face="normal" font="default" size="100%">Sunil Kumar</style></author><author><style face="normal" font="default" size="100%">Neeraj Mahindroo</style></author><author><style face="normal" font="default" size="100%">Reena Vohra Saini</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bioactive Fraction from Datura stramonium Linn. Promotes Human immune Cells Mediated Cytotoxicity towards Lung and Breast Cancer Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anticancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytokine</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxic</style></keyword><keyword><style  face="normal" font="default" size="100%">Datura stramonium.</style></keyword><keyword><style  face="normal" font="default" size="100%">Immunomodulation</style></keyword><keyword><style  face="normal" font="default" size="100%">PBMC</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Oct 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">435-439</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aim: &lt;/strong&gt;The aim of the present study was to evaluate immune modulatory effect of fractions of &lt;em&gt;D. stramonium&lt;/em&gt; L. leaves on human peripheral blood mononuclear cells (PBMC) followed by assessment of cytotoxic abilities of immunomodulated PBMC toward cancer cells. &lt;strong&gt;Material and methods: &lt;/strong&gt;Bioassay (PBMC proliferation) guided fractionation of methanolic leaf extract of &lt;em&gt;D. stramonium&lt;/em&gt; was performed to get active fraction and LC-MS was performed to identify the phytocompounds present in the bioactive fraction. The immunomodulatory potential of&lt;em&gt; D.&lt;/em&gt; &lt;em&gt;stramonium&lt;/em&gt; active fraction was assessed by i) MTT microcytotoxicity assay using A549 (lung carcinomas) and MCF-7 (breast cancer) cell lines and ii) analyzing the production of IL-2 and IFN-&amp;gamma; by human PBMC in the presence of active fraction. &lt;strong&gt;Results:&lt;/strong&gt; Chromatographic fractionation guided by PBMC proliferation assay of &lt;em&gt;D. stramonium&lt;/em&gt; extract resulted in bioactive fraction (fraction-10) exhibiting significant immunostimulatory activity [EC&lt;sub&gt;50&lt;/sub&gt;=19.1&amp;plusmn;1.5 (&amp;mu;g/ml)] on human blood lymphocytes. Fraction-10 pretreated PBMC displayed enhanced cytotoxicity towards A549 and MCF-7 (59%&amp;plusmn;2.1% and 62%&amp;plusmn;2.3% at 1:20 effector:target ratio respectively). Moreover, fraction-10 also enhanced the secretion of IL-2 (8 fold) and IFN-&amp;gamma; (10 fold) by human PBMC. The preliminary phytochemical analysis of fraction-10 from&lt;em&gt; D. stramonium&lt;/em&gt; showed the presence of terpenoids and steroids. LC-MS analysis depicted presence of four major phytoconstituents in fraction-10 as daturaolone, daturadiol, stigmasterol and sitosterol with corresponding mass spectrum (m/z) of 440, 442, 412 and 414 respectively. &lt;strong&gt;Conclusion: &lt;/strong&gt;The present report concluded that active fraction-10 of&lt;em&gt; D. stramonium&lt;/em&gt; possesses potential immunostimulators that are capable of enhancing anticancer responses of human blood lymphocytes.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">435</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Aditi Gupta&lt;sup&gt;1&lt;/sup&gt;, Sunil Kumar&lt;sup&gt;2&lt;/sup&gt;, Neeraj Mahindroo&lt;sup&gt;2&lt;/sup&gt;, Reena Vohra Saini&lt;sup&gt;1*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Animal Biotechnology Laboratory, Faculty of Applied Sciences and Biotechnology, Shoolini University, Himachal Pradesh, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacology Laboratory, Faculty of Pharmaceutical Sciences, Shoolini University, Himachal Pradesh, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jitender Singh</style></author><author><style face="normal" font="default" size="100%">Ashwani Kumar</style></author><author><style face="normal" font="default" size="100%">Anupam Sharma</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bioactivity Guided Fractionation of Ethanol Extract of Caesalpinia digyna Rottler Roots</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antianxiety</style></keyword><keyword><style  face="normal" font="default" size="100%">Bioactivity-guided fractionation</style></keyword><keyword><style  face="normal" font="default" size="100%">Caesalpinia digyna</style></keyword><keyword><style  face="normal" font="default" size="100%">Elevated plus-maze.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">165-167</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Authors have reported earlier that ethanol extract of &lt;em&gt;Caesalpinia digyna&lt;/em&gt; Rottler roots exhibits significant antianxiety activity at 400 mg/kg, po, in mice using elevated plus-maze (EPM).&lt;strong&gt; Objective&lt;/strong&gt;: Aim of the study was to isolate antianxiety principle(s) from ethanol extract of &lt;em&gt;C. digyna&lt;/em&gt; roots following bioactivity guided fractionation approach. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Bioactive ethanol extract was partitioned with ethyl acetate to get ethyl acetate soluble (EASF) and ethyl acetate insoluble (EAIF) fractions. A compound (CD&lt;sub&gt;1&lt;/sub&gt;) precipitated from EASF. The two fractions and CD&lt;sub&gt;1&lt;/sub&gt; were evaluated for antianxiety activity in mice. Column chromatography of EASF yielded 5 fractions (F&lt;sub&gt;1&lt;/sub&gt;-F&lt;sub&gt;5&lt;/sub&gt;), all of which were evaluated for antianxiety activity using EPM.&lt;strong&gt; Results:&lt;/strong&gt; Present study revealed that EASF (80 mg/kg) and CD&lt;sub&gt;1&lt;/sub&gt; (40 mg/kg) exhibited significant antianxiety activity, while EAIF does not. Among the five fractions, only F4 (40 mg/kg, po), exhibited significant antianxiety activity, which was statistically comparable to that of diazepam (2 mg/kg). &lt;strong&gt;Conclusion: &lt;/strong&gt;Present investigation reveals that EASF obtained by partitioning of ethanol extract of &lt;em&gt;C. digyna &lt;/em&gt;roots with ethyl acetate, and a compound CD&lt;sub&gt;1&lt;/sub&gt;, isolated from EASF, exhibit significant antianxiety activity. Among 5 fractions (F&lt;sub&gt;1&lt;/sub&gt;-F&lt;sub&gt;5&lt;/sub&gt;) obtained from column chromatography of EASF, only F4 exhibited significant antianxiety activity. F4 is being processed further to isolate the anxiolytic constituent(s), and CD&lt;sub&gt;1&lt;/sub&gt; is being characterized.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">165</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Jitender Singh, Ashwani Kumar*, Anupam Sharma&lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;Department of Pharmacognosy, University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh-160014, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&amp;nbsp;&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kumara Shanthamma Kavitha</style></author><author><style face="normal" font="default" size="100%">Sreedharamurthy Satish</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bioprospecting of some medicinal plants explored for antifungal activity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">09/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">59-65</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;In the present study, evaluation of different plant parts of fifteen medicinal plants belongs to different families have been screened for &lt;em&gt;in vitro&lt;/em&gt; efficacy of antifungal activity against phyto pathogenic (&lt;em&gt;Aspergillus&lt;/em&gt; and &lt;em&gt;Fusarium&lt;/em&gt; species) as well as human pathogenic fungi (&lt;em&gt;Candida albicans&lt;/em&gt; and &lt;em&gt;Microsporum&lt;/em&gt; species) using agar well diffusion assay. The results showed that among fifteen medicinal plants, crude extracts of different solvents viz., petroleum ether, chloroform, ethyl acetate and methanol tested for antifungal activity, twelve plants were found to be effective against one or the other test fungi, among these plants, solvent extracts of &lt;em&gt;Callistemon lanceolatus&lt;/em&gt; showed significant activity against &lt;em&gt;C&lt;/em&gt;. &lt;em&gt;albicans&lt;/em&gt;, &lt;em&gt;Microsporum gypseum&lt;/em&gt;, &lt;em&gt;Cordia dichrotoma&lt;/em&gt; leaves extracts exhibited significant activity against &lt;em&gt;A&lt;/em&gt;. &lt;em&gt;niger&lt;/em&gt;, &lt;em&gt;A&lt;/em&gt;. &lt;em&gt;flavus&lt;/em&gt; and &lt;em&gt;C&lt;/em&gt;. &lt;em&gt;albicans&lt;/em&gt;. &lt;em&gt;Sphaeranthus indicus&lt;/em&gt; L. whole plant extracts exhibited significant activity against &lt;em&gt;Aspergillus&lt;/em&gt; spp.,&lt;em&gt; C&lt;/em&gt;. &lt;em&gt;albicans&lt;/em&gt; and &lt;em&gt;Microsporum&lt;/em&gt; &lt;em&gt;canis&lt;/em&gt;. Leaves extracts of &lt;em&gt;Vitex negundo&lt;/em&gt; exhibited significant activity against &lt;em&gt;A&lt;/em&gt;. &lt;em&gt;niger&lt;/em&gt;, &lt;em&gt;A&lt;/em&gt;. &lt;em&gt;flavus&lt;/em&gt;, &lt;em&gt;F&lt;/em&gt;. &lt;em&gt;verticillioides&lt;/em&gt;, &lt;em&gt;C&lt;/em&gt;. &lt;em&gt;albicans&lt;/em&gt; and moderate activity against &lt;em&gt;F&lt;/em&gt;. &lt;em&gt;crookwellense&lt;/em&gt;. Extracts of &lt;em&gt;Butea monosperma&lt;/em&gt; exhibited significant to moderate activity against all test pathogens except &lt;em&gt;C&lt;/em&gt;. &lt;em&gt;albicans&lt;/em&gt;. The obtained results imparts a preliminary piece of significant information regarding the antifungal potentiality of screened medicinal plants and thus our present investigation depicted an outline interpretation of significant activity with crude solvent extracts, which could be exploit for further isolation and investigation of antifungal agents for crop diseases management and human health.&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Keywords:&lt;/strong&gt; Nill&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">59</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Kumara Shanthamma Kavitha and Sreedharamurthy Satish*&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;Herbal Drug Technological Laboratory, Department of Studies in Microbiology, University of Mysore, Manasagangotri, Mysore 570 006 Karnataka, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Anusha T S</style></author><author><style face="normal" font="default" size="100%">Joseph M V</style></author><author><style face="normal" font="default" size="100%">Elyas K K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Callus Induction and Elicitation of Total Phenolics in Callus Cell Suspension Culture of Celastrus paniculatus – willd, an Endangered Medicinal Plant in India</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Bioactive constituents</style></keyword><keyword><style  face="normal" font="default" size="100%">Callogenesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Celastrus paniculatus</style></keyword><keyword><style  face="normal" font="default" size="100%">Elicitors</style></keyword><keyword><style  face="normal" font="default" size="100%">Total phenolics.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Oct 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">471-475</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;em&gt;Celastrus paniculatus&lt;/em&gt; - Willd belonging to the family Celastraceae is a vulnerable medicinal plant in India. It has been employed as a stimulant, nervine tonic, rejuvenant, sedative, tranquilizer and diuretic. It is also used in the treatment of leprosy, leucoderma, rheumatism, gout, paralysis and asthma. Because of its high pharmaceutical application, this plant species were over exploited and now considered under threatened species. So the highlight of the present investigation is the induction of callus by using different concentration of various phytohormones such as 2, 4-D (0.5 - 3.0 mg/l) and NAA (0.5 - 2.5 mg/l). In order to ensure the presence of the bioactive compounds preliminary phytochemical screening of the various extracts of callus were performed. Finally elicitation of total phenolics were done in callus cell suspension cultures by using elicitors such as jasmonic acid, salicylic acid and copper sulphate. Among the applied elicitors jasmonic acid showed superiority. To our knowledge, this is the first report of the elicitation of secondary metabolites especially total phenolics from callus cell suspension cultures of &lt;em&gt;Celastrus Paniculatus.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">471</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Anusha T S, Joseph M V and Elyas K K&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;Department of Biotechnology, University of Calicut, Thenjipalam, Kerala, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lavanya Kakarla</style></author><author><style face="normal" font="default" size="100%">Rajath Othayoth</style></author><author><style face="normal" font="default" size="100%">Mahendran Botlagunta</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Biochemical Studies on Indian Sedges Cyperus scariosus R.Br and Cyperus rotundus L.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">EDAX (Energy Dispersive X-ray Analysis) and COX-2 (Cyclooxygenase- 2).</style></keyword><keyword><style  face="normal" font="default" size="100%">GC-MS (Gas chromatography and Mass Spectroscopy)</style></keyword><keyword><style  face="normal" font="default" size="100%">SEM (Scanning Electron Microscopy)</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">598-609</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Cyperus scariosus&lt;/em&gt; R.Br and &lt;em&gt;Cyperus rotundus &lt;/em&gt;L are well known Indian medicinal plants in ayurveda and herbal industry. These two species are often treated as synonymous to each other, although they grow in different agro climatic conditions. &lt;strong&gt;Objective: &lt;/strong&gt;In the present study, we made an attempt on comparative biochemical studies among these two species by using various spectroscopic, analytical and &lt;em&gt;in silico&lt;/em&gt; molecular docking studies.&lt;strong&gt; Materials and Methods:&lt;/strong&gt; Rhizome methanolic extracts of both the species were subjected to GC-MS and elemental analysis to identify the presence of phytochemical constituents and trace elements respectively. Following confirmation, the identified compounds were subjected to molecular docking analysis using anti-inflammatory protein COX-2 as the target receptor. Further these extracts were encapsulated into biodegradable chitosan nanoparticles and they were characterised using SEM and FT-IR analysis. Finally, the antioxidant and anti-inflammatory activity of these extract loaded nanoparticles were evaluated using &lt;em&gt;in vitro &lt;/em&gt;assays.&lt;strong&gt; Results: &lt;/strong&gt;Compounds present in both plant extracts form strong hydrogen bond interactions with COX-2. SEM analysis of &lt;em&gt;C. scariosus &lt;/em&gt;showed chitosan nanoparticles are spherical in shape. Whereas &lt;em&gt;C. rotundus&lt;/em&gt; forms aggregates, although they are well-dispersed in water following lyophilisation. FT-IR analysis showed that both plant extracts have different compounds, which is evident from the wavelength difference and their shift pattern as compared to blank nanoparticles. In spite of the differences, both of the drug encapsulated plant extracts showed good antioxidant and anti-inflammatory properties. &lt;strong&gt;Conclusion:&lt;/strong&gt; &lt;em&gt;C. scariosus&lt;/em&gt; and &lt;em&gt;C. rotundus&lt;/em&gt; are different, but similar with some of the phytochemical constituents and pharmaceutical values.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">598</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Lavanya Kakarla, Rajath Othayoth and Mahendran Botlagunta* &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;Biomedical Research Laboratory, Department of Biotechnology, K L E F University, Vaddeswaram, Guntur-522502, Andhra Pradesh, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sunita Shailajan</style></author><author><style face="normal" font="default" size="100%">Suman Kumaria</style></author><author><style face="normal" font="default" size="100%">Suhas Pednekar</style></author><author><style face="normal" font="default" size="100%">Sasikumar Menon</style></author><author><style face="normal" font="default" size="100%">Hiranjit Choudhury</style></author><author><style face="normal" font="default" size="100%">Archana Matani</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Estrogenic Potential of Flemingia vestita Benth Tubers in Ovariectomized Rat Model</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Estrogenic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Flemingia vestita</style></keyword><keyword><style  face="normal" font="default" size="100%">genistein</style></keyword><keyword><style  face="normal" font="default" size="100%">HPLC</style></keyword><keyword><style  face="normal" font="default" size="100%">ovariectomized rats.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">09/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">44-49</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective: &lt;/strong&gt;This study investigates the potential estrogenic activity of the ethanolic extract of &lt;em&gt;Flemingia vestita&lt;/em&gt; Benth tubers using ovariectomized rat model.&lt;strong&gt; Materials and Methods:&lt;/strong&gt; The ethanolic extract of &lt;em&gt;F. vestita&lt;/em&gt; tubers has been standardized using validated HPLC method in terms of its genistein content (8.43 &amp;plusmn; 0.05 mg/g of extract). Three to four week old young albino Wistar female rats were ovariectomized and treated for 14 days post ovariectomy with the standardized ethanolic extract at three different dose levels (100, 250, 500 mg/kg body weight) with a positive control of Estradiol valerate (1 mg/kg/day). The parameters evaluated were uterine weight, uterine glycogen, G6PDH, LDH, 17&amp;beta;-estradiol, progesterone, total cholesterol, triglycerides, HDL and histo architecture of uterus. &lt;strong&gt;Results:&lt;/strong&gt; Treatment with the ethanolic extract of &lt;em&gt;F. vestita &lt;/em&gt;tubers showed dose dependent increase in uterine weight, glycogen levels, G6PDH levels, estrogen and progesterone levels when compared with the ovariectomized control. Amongst three dose levels, high dose of plant extract showed significant increase in the uterine weight (p &amp;lt; 0.001), uterine glycogen content (p &amp;lt; 0.001), 17-&amp;beta; estradiol and progesterone levels (p &amp;lt; 0.001), G6PDH and LDH levels (p &amp;lt; 0.001) as well as significant decrease in HDL and triglycerides levels (p &amp;lt; 0.001) compared to ovariectomized control. Histopathological evaluation of uteri sections revealed that the high dose of the plant show increase in the endometrial response as indicated by proliferation of endometrial glands and luminal epithelium of the ovariectomized rats. &lt;strong&gt;Conclusion:&lt;/strong&gt; Thus, these data suggests that ethanolic extract (500 mg/kg body weight) of &lt;em&gt;F. vestita&lt;/em&gt; tubers may exhibit good estrogenic activity in ovariectomized rat model.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Estrogenic activity, &lt;em&gt;Flemingia vestita&lt;/em&gt;, genistein, HPLC, ovariectomized rats.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">44</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;margin-left: 9pt; text-align: justify;&quot;&gt;&lt;strong&gt;Sunita Shailajan&lt;sup&gt;1*&lt;/sup&gt;, Suman Kumaria&lt;sup&gt;2&lt;/sup&gt;, Suhas Pednekar&lt;sup&gt;1&lt;/sup&gt;, Sasikumar Menon&lt;sup&gt;3&lt;/sup&gt;,&lt;/strong&gt;&lt;strong&gt; Hiranjit Choudhury&lt;sup&gt;2&lt;/sup&gt; and Archana Matani&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Herbal Research Lab, Ramnarain Ruia College, Matunga (East), Mumbai - 400019, India.&lt;sup&gt; &lt;/sup&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Botany, North-Eastern Hill University, Umshing Mawkynroh, Shillong - 793022, Meghalaya, India.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Institute for Advanced Training and Research in Interdisciplinary Sciences, 194, Scheme No. 6, Road No. 15, Sion Koliwada, Sion (E), Mumbai - 400022, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mrinmoy Nag</style></author><author><style face="normal" font="default" size="100%">Pulok k Mukherjee</style></author><author><style face="normal" font="default" size="100%">Rajarshi Biswas</style></author><author><style face="normal" font="default" size="100%">Joydeb Chanda</style></author><author><style face="normal" font="default" size="100%">Amit Kar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Antimicrobial Potential of Some Indian Ayurvedic Medicinal Plants</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ananas comosus Merrill</style></keyword><keyword><style  face="normal" font="default" size="100%">Annona squamosa</style></keyword><keyword><style  face="normal" font="default" size="100%">Antibacterial</style></keyword><keyword><style  face="normal" font="default" size="100%">Capsicum annuum cayenne</style></keyword><keyword><style  face="normal" font="default" size="100%">Stereospermum suaveolens Roxb</style></keyword><keyword><style  face="normal" font="default" size="100%">Viscum articulatum Burm.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">525-533</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Stereospermum suaveolens&lt;/em&gt; Roxb., &lt;em&gt;Viscum articulatum&lt;/em&gt; Burm., &lt;em&gt;Annona squamosa, Capsicum annuum&lt;/em&gt; cayenne, &lt;em&gt;Ananas comosus&lt;/em&gt; Merrill. are used for the management of microbial infection in Ayurveda. The present study was designed to standardize the extract of &lt;em&gt;S. suaveolens&lt;/em&gt; bark (SSB), &lt;em&gt;V. articulatum&lt;/em&gt; aerial part (VAAP), &lt;em&gt;A. squamosa&lt;/em&gt; leaf (ASL), &lt;em&gt;C. annuum&lt;/em&gt; fruit (CACF), &lt;em&gt;A. comosus&lt;/em&gt; fruit (ACF) and performed antibacterial activity. &lt;strong&gt;Methods: &lt;/strong&gt;The antibacterial activity of the five extracts were evaluated against certain bacteria such as &lt;em&gt;B. subtilis, B. cereus, S. aureus &lt;/em&gt;(gram positive); &lt;em&gt;E. coli, S. typhi,&lt;/em&gt; and &lt;em&gt;P. aureugenosa&lt;/em&gt; (gram negative) by disc diffusion method, time course assay, pH sensitivity assay and minimum inhibitory concentration (MICs) through broth micro-dilution method. &lt;strong&gt;Results: &lt;/strong&gt;The plants extracts VAAP, ASL, and CACF showed potent inhibitory activity against &lt;em&gt;S. aureus&lt;/em&gt; with MIC 728, 742, and 698 &lt;em&gt;&amp;mu;&lt;/em&gt;g ml&lt;sup&gt;-1&lt;/sup&gt;, respectively, while CACF showed inhibitory activity against &lt;em&gt;B. subtilis&lt;/em&gt; with MIC 690 &lt;em&gt;&amp;mu;&lt;/em&gt;g ml&lt;sup&gt;-1&lt;/sup&gt;. The results further demonstrated that the inhibitory activity of CACF against &lt;em&gt;E. coli &lt;/em&gt;with MIC 760 &lt;em&gt;&amp;mu;&lt;/em&gt;g ml&lt;sup&gt;-1&lt;/sup&gt;. &lt;em&gt;P. aeruginosa&lt;/em&gt; was inhibited by ASL and CACF with MIC 1100 and 1120 &lt;em&gt;&amp;mu;&lt;/em&gt;g ml&lt;sup&gt;-1&lt;/sup&gt;, respectively. The ASL showed notable MBC against the tested microorganism. Moreover, all extracts were completely inactivated bacterial strains (except &lt;em&gt;B. cereus, S. typhi&lt;/em&gt;) within 2-10 h of exposure, determined by time course assay. &lt;strong&gt;Conclusion: &lt;/strong&gt;The outcomes of our study elucidate that standardized extracts of &lt;em&gt;A. comosus, A. squamosa, C. annuum, S. suaveolens, &lt;/em&gt;and&lt;em&gt; V. articulatum&lt;/em&gt; may be used as natural antimicrobial agents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">525</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Mrinmoy Nag, Pulok k Mukherjee *, Rajarshi Biswas, Joydeb Chanda, Amit Kar &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Pharmaceutical Technology, Jadavpur University, Kolkata-700032, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zahoor Ahmad Rather</style></author><author><style face="normal" font="default" size="100%">Nateshprabhu M</style></author><author><style face="normal" font="default" size="100%">Sushma DS</style></author><author><style face="normal" font="default" size="100%">Rakesh Kb</style></author><author><style face="normal" font="default" size="100%">Sunil Pai</style></author><author><style face="normal" font="default" size="100%">Ullal sheetal D</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of Costus speciosus in Experimental Models of Depression in Albino Mice</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antidepressant</style></keyword><keyword><style  face="normal" font="default" size="100%">Costus speciosus</style></keyword><keyword><style  face="normal" font="default" size="100%">Forced swim test</style></keyword><keyword><style  face="normal" font="default" size="100%">Tail suspension</style></keyword><keyword><style  face="normal" font="default" size="100%">Test.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Oct 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">483-486</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Despite theavailability of numerous antidepressant drugs the therapy of depression is far from satisfactory. Two of the many reasons for this are the delay in onset of effect and the adverse effects associated with most of the antidepressants. &lt;em&gt;Costus speciosus&lt;/em&gt; rhizome has shown adaptogenic activity. &lt;strong&gt;Objective: &lt;/strong&gt;To evaluate the antidepressant activity of50% aqueous-ethanol extract of &lt;em&gt;Costus speciosus&lt;/em&gt; (CS) leaves in experimental models of depression.&lt;strong&gt; Materials and Methods:&lt;/strong&gt; Male albino mice were randomly assigned to five groups of six each. We studied three doses of the leaf extract (100, 200 and 400 mg/kg) on two models of depression &amp;ndash; forced swim test and tail suspension test. Imipramine was used as the standard control. Both acute and chronic effects were studied. Drugs (test drug, standard control and vehicle) were administeredorally, one hour before the experiment in the acute study and daily for 14 days for the chronic study. &lt;strong&gt;Results:&lt;/strong&gt; Imipramine showed significant antidepressant activity as demonstrated by a reduction in duration of immobility in both acute and chronic studies of forced swim test and tail suspension test. CS showed a dose dependent antidepressant activity. CS_100 demonstrated an antidepressant effect only in the acute forced swim test. CS_200 demonstrated an antidepressant activity in both acute and chronic forced swim test but not in tail suspension test. CS_400 showed maximum antidepressant activity in both acute and chronic studies, which was comparable to that of the standard drug imipramine.&lt;strong&gt; Conclusion:&lt;/strong&gt; CS showed dose dependent antidepressant activity with CS_400 mg/kg showing maximum effect.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">483</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Zahoor Ahmad Rather&lt;sup&gt;1&lt;/sup&gt;, Nateshprabhu M&lt;sup&gt;2&lt;/sup&gt;, Sushma DS&lt;sup&gt;3&lt;/sup&gt;, Rakesh Kb&lt;sup&gt;1&lt;/sup&gt;, Sunil Pai&lt;sup&gt;1&lt;/sup&gt;, Ullal Sheetal D&lt;sup&gt;1*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, Kasturba Medical College, Mangalore, Manipal University, Karnataka, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology, Dhanalakshmi Srinivasan Medical College and Hospital, Perambalur, TamilNadu, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacology, Khaja Banda nawaz Institute of Medical Sciences, Kalburgi Karnataka, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohammad Ali</style></author><author><style face="normal" font="default" size="100%">Mruthunjaya Kenganora</style></author><author><style face="normal" font="default" size="100%">Santhepete Nanjundaiah Manjula</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Health Benefits of Morinda citrifolia (Noni): A Review</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anticancer.</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Morinda citrifolia</style></keyword><keyword><style  face="normal" font="default" size="100%">Neutraceutical</style></keyword><keyword><style  face="normal" font="default" size="100%">Phyto-constituents</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June/2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">321-334</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Morinda citrifolia &lt;/em&gt;(Noni) has been used widely as a complementary and alternative therapy in many countries owing to its potent antioxidant activity and proven health benefits. Traditionally, it finds used as a therapeutic remedy to various diseases as an antibacterial, antitumor, anthelminthic, analgesic, anti-inflammatory, immunostimulant. Also it has proved beneficial in conditions like gastritis, skin diseases, respiratory infections, menstrual and urinary tract disorders, fever, diabetes and venereal diseases. &lt;strong&gt;Objective:&lt;/strong&gt; This review emphasizes on the phytochemical and mineral profile of the different parts of Noni plant. In addition, this review corroborates the pharmacological basis for the various health benefits, traditional and medicinal applications of Noni. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; All the available information of Noni were collected from electronic databases such as Academic Journals, Ethnobotany, Ethnopharmacology, Springer, PubMed, Google Scholar, Science Direct and other primary and secondary sources.&lt;strong&gt; Results:&lt;/strong&gt; According to our search results pertaining to scientific literature, &lt;em&gt;Morinda citrifolia&lt;/em&gt; is used for more than 40 types of ailments worldwide. Crude extract of various parts of plant and fruit juice are reported to contain amino acids, anthraquinones, fatty acids, flavonoids, iridoids, lignans, polysaccharides, sterols, sugars, terpenoids etc. which are therapeutically useful for a broad range of pathological conditions. Fourteen human clinical trials have validated the remarkable health benefits of Noni. &lt;strong&gt;Conclusion:&lt;/strong&gt; Literatures prove that Noni is pharmacologically active and is used in different forms of cancer, viz. colon, esophageal, breast, colorectal cancers; cardiovascular diseases, diabetes, arthritis, hypertension. These properties are substantiated by the preclinical or/and clinical investigations.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">321</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Mohammad Ali, Mruthunjaya Kenganora, Santhepete Nanjundaiah Manjula* &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Pharmacology, JSS College of Pharmacy, JSS University, Sri Shivarathreeshwara Nagar- 570015, Dist-Mysore, State- Karnataka, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Varsha Raj</style></author><author><style face="normal" font="default" size="100%">Arun Kumar Mishra</style></author><author><style face="normal" font="default" size="100%">Amrita Mishra</style></author><author><style face="normal" font="default" size="100%">Najam Ali Khan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hepatoprotective effect of Prunus armeniaca L. (Apricot) leaf extracts on Paracetamol induced liver damage in Wistar rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Apricot</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Liver toxicity.</style></keyword><keyword><style  face="normal" font="default" size="100%">Paracetamol</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">154-158</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Objective&lt;/strong&gt;: To evaluate the hepatoprotective effect of &lt;em&gt;Prunus armeniaca&lt;/em&gt; L. (Apricot) leaf on paracetamol induced liver toxicity in rats. &lt;strong&gt;Method: &lt;/strong&gt;Phytochemical investigation was performed to find active constituents of the plant extracts by the different phytochemical tests. After induction of liver toxicity, the biochemical parameters such as serum glutamic pyruvic transaminase (sGPT), serum glutamic oxaloacetic transaminase (sGOT), serum alkaline phosphatase (sALP), serum bilirubin (SB), thiobarbituric acid reactive substances (TBARS), &amp;gamma;-glutamyl transferase (GGT), lactate dehydrogenase (LDH), total protein (TP), albumin. The physical parameters including liver weight, body weight and histopathological changes in the liver were studied with Ursodeoxycholic acid as standard hepatoprotective agents.&lt;strong&gt; Results: &lt;/strong&gt;The phytochemical investigation of the extracts showed the presence of Alkaloids, volatile oil, saponin glycosides, condensed tanins, terpenoids, steroids and flavonoids. Methanol and aqueous extract before the paracetamol administration caused a significant reduction in the values of sGOT, sGPT, sALP, TBARS, GGT, LDH TP, Albumin and sB (P&amp;lt;0.01) almost comparable to the Ursodeoxycholic acid. The hepatoprotective activity was confirmed by histopathological examination of the liver tissue of control and treated animals. &lt;strong&gt;Conclusions:&lt;/strong&gt; The result concludes that &lt;em&gt;Prunus armeniaca&lt;/em&gt; L. possesses the hepatoprotective effect against paracetamol induced liver toxicity in rats.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">154</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Varsha Raj*, Arun Kumar Mishra, Amrita Mishra, Najam Ali Khan&lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;Department of Pharmacy, Pharmacology Research Lab, IFTM University, Moradabad, 244102, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Badarinath Druvarao Kulkarni</style></author><author><style face="normal" font="default" size="100%">Samim Sultana</style></author><author><style face="normal" font="default" size="100%">Mayuri Bora</style></author><author><style face="normal" font="default" size="100%">Ishita Dutta</style></author><author><style face="normal" font="default" size="100%">Padmaa Milaap Paarakh</style></author><author><style face="normal" font="default" size="100%">Vedamurthy Ankala Basappa.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">In vitro Cytotoxicity Studies of Zn (Zinc) Nanoparticles Synthesized from Abutilon indicum L. against Human Cervical Cancer (HeLa) Cell Lines.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Abutilon indicum</style></keyword><keyword><style  face="normal" font="default" size="100%">Cervical cancer</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">MTT Assay</style></keyword><keyword><style  face="normal" font="default" size="100%">Zn nanoparticles</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">127-131</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; The Zn nanoparticles synthesized from the plant sources are ecofriendly and are potent anticancer agents. &lt;strong&gt;Objective&lt;/strong&gt;: The objective of the present work was to evaluate &lt;em&gt;In vitr&lt;/em&gt;o cytotoxic activity of Zn nanoparticles green synthezised from &lt;em&gt;Abutilon indicu&lt;/em&gt;m extract against HeLa cell lines (cervical cancer). &lt;strong&gt;Methods:&lt;/strong&gt; The aqueous extract is prepared by cold extraction (maceration) using water as a solvent. Phytochemical analysis was done by using the standard procedures. Aqueous extract of &lt;em&gt;A. indicum&lt;/em&gt; was used for synthesis of Zn nanoparticles. The nanoparticles were characterized by UV-Visible spectrometry and Scanning electron microscopy (SEM) techniques. &lt;em&gt;In vitro&lt;/em&gt; cytotoxicity studies of Zn nanoparticles were done by MTT assay using HeLa cell lines. &lt;strong&gt;Results:&lt;/strong&gt; The preliminary phytochemical results revealed that the aqueous extract of &lt;em&gt;A. indicum&lt;/em&gt; contains broad spectrum of secondary metabolites like Tannins, Saponins, Glycosides, Flavonoids, Anthroquinones, Terpenoids and Steroids. The U.V spectrophotometeric analysis of Zn nanoparticles displayed maximum absorption at 270 nm and scanning electron microscopic studies showed that the nanoparticles size ranges from 50-500 nm. The MTT assay results revealed that the of Zn nanoparticles exhibits potent cytotoxicity against HeLa cell lines with IC&lt;sub&gt;50&lt;/sub&gt; value of 45.82 &amp;mu;g/ml. &lt;strong&gt;Conclusion:&lt;/strong&gt; Thus the present study concludes that Zn nanoparticles can be used as a potent drug in alternative therapy for treating the cervical cancer patients.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">127</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Badarinath Druvarao Kulkarni&lt;sup&gt;1&lt;/sup&gt;, Samim Sultana&lt;sup&gt;2&lt;/sup&gt;, Mayuri Bora&lt;sup&gt;2&lt;/sup&gt;, Ishita Dutta&lt;sup&gt;2&lt;/sup&gt;, Padmaa Milaap Paarakh&lt;sup&gt;3&lt;/sup&gt;, Vedamurthy Ankala Basappa&lt;sup&gt;1&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biotechnology and Microbiology, Karnatak University, Dharwad, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biotechnology, The Oxford College of Science, Bangalore, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacognosy, The Oxford College of Pharmacy, Bangalore-560 068, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dinesh Kumar Yadav</style></author><author><style face="normal" font="default" size="100%">Mohammed Ali</style></author><author><style face="normal" font="default" size="100%">Ashoke Kumar Ghosh</style></author><author><style face="normal" font="default" size="100%">Babita Kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Isolation of flavonoid from Abies webbiana leaves and its activity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">1-H NMR</style></keyword><keyword><style  face="normal" font="default" size="100%">Abies webbiana</style></keyword><keyword><style  face="normal" font="default" size="100%">CCl4.</style></keyword><keyword><style  face="normal" font="default" size="100%">Cisplatin</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercetin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June/2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">341-345</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Abies webbiana &lt;/em&gt;commonly known as Talispatra in Bengali and Hindi, Talispatram in Sanskrit and Indian Silver Fir in English. This is a large, tall, evergreen tree occurring in the Himalayan region from Kashmir to Assam in India. It comes under the Family: Pinaceae. The present study was designed for isolation of flavonoid from ethyl acetate extract of &lt;em&gt;A. webbiana&lt;/em&gt; leaves and assessed their toxic effect on liver and kidney. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The isolation of flavonoid using different chromatographic methods (thin layer and column chromatography). The isolated flavonoid was identified; Structures and chemical bonds were analyzed by using MP, FTIR, 1-H NMR and MS spectral analysis. Effect of flavonoid on liver and kidney was assessed by inducing (0.1 ml/kg) CCl&lt;sub&gt;4&lt;/sub&gt; (i.p.) and (6 mg/kg) Cisplatin (i.p.) respectively measured by biochemical marker of liver and kidney. &lt;strong&gt;Results and Discussion: &lt;/strong&gt;It was identified that isolated compound was as 4&amp;rsquo;-hydroxy quercetin on the basis of FTIR, 1-H NMR and MS spectral analysis. Isolated flavonoid reduced the increased biochemical marker (BM) of liver and kidney. The BM was increased by inducing CCl&lt;sub&gt;4&lt;/sub&gt; and Cisplatin respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; Isolated compound was 4&amp;rsquo;-methoxy quercetin and significantly protect the liver and kidney.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">341</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Dinesh Kumar Yadav&lt;sup&gt;1&lt;/sup&gt;*, Mohammed Ali&lt;sup&gt;2&lt;/sup&gt;, Ashoke Kumar Ghosh&lt;sup&gt;3&lt;/sup&gt;, Babita Kumar&lt;sup&gt;1&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;College of Pharmacy, Shree Ganpati Institute of Technology, Ghaziabad (U.P.), INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacognosy &amp;amp; Phytochemistry, Phytochemistry Research Laboratory, Faculty of Pharmacy, Jamia Hamdard, Hamdard Nagar, New Delhi 110062, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;School of Pharmaceutical Sciences, IFTM University, Moradabad (U.P.), INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kalpna Rakholiya</style></author><author><style face="normal" font="default" size="100%">Mital Kaneria</style></author><author><style face="normal" font="default" size="100%">Sumitra Chanda</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Physicochemical and Phytochemical Analysis of Different Parts of Indian Kesar Mango–A unique variety from Saurashtra Region of Gujarat</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Kesar Mango</style></keyword><keyword><style  face="normal" font="default" size="100%">Physicochemical parameters</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Ripe and Unripe Peel</style></keyword><keyword><style  face="normal" font="default" size="100%">Ripe and Unripe Seeds</style></keyword><keyword><style  face="normal" font="default" size="100%">Stem.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Oct 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">502-506</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;The aim of the present study was to evaluate physicochemical and phytochemical analysis of different parts (ripe seed, unripe seed, ripe peel, unripe peel and stem) of Indian mango (var. &amp;lsquo;&lt;em&gt;Kesar&lt;/em&gt;&amp;rsquo;) collected from Saurashtra region of Gujarat. The physiochemical properties such as loss on drying, total ash value, acid insoluble ash value, water soluble ash value and extractive values were carried out. The phytochemical properties such as alkaloids, flavonoids, tannins, phlobatanins, triterpenes, steroids, saponins and cardiac glycosides were also carried out. In phytochemical analysis, tannins showed maximum amounts in all five parts. The present study provides the details physicochemical and phytochemical properties of different parts of kesar mango which are useful in laying down standardization and pharmacopeia parameters.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">502</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Kalpna Rakholiya*, Mital Kaneria and Sumitra Chanda&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;Department of Biosciences, Saurashtra University, Rajkot-360 005, Gujarat, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tanayen Julius Kihdze</style></author><author><style face="normal" font="default" size="100%">Ajayi Abayomi Mayowa</style></author><author><style face="normal" font="default" size="100%">Oloro Joseph</style></author><author><style face="normal" font="default" size="100%">Ezeonwumelu Joseph OC</style></author><author><style face="normal" font="default" size="100%">Tanayen Grace Ghaife</style></author><author><style face="normal" font="default" size="100%">Adzu Bulus</style></author><author><style face="normal" font="default" size="100%">Arthur van Aerschot</style></author><author><style face="normal" font="default" size="100%">Gert Laekeman</style></author><author><style face="normal" font="default" size="100%">Agaba Amon Ganafa</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical and Antidiabetic Evaluation of the Methanolic Stem Bark Extract of Spathodea campanulata (P. Beauv.) Bignoniaceae</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Saponins</style></keyword><keyword><style  face="normal" font="default" size="100%">Spathodea campanulata (P. Beauv.) Bignoniaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">TLC Tannins</style></keyword><keyword><style  face="normal" font="default" size="100%">Uganda.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan/2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">243-249</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background&lt;/strong&gt;: &lt;em&gt;Spathodea campanulata (P. Beauv.) Bignoniaceae &lt;/em&gt;extract&amp;nbsp;(SCE) is one of many herbal medicines&amp;nbsp;used widely in Ugandan traditional&amp;nbsp;medicine for various ailments. Generally most of these herbal&amp;nbsp;medicines&amp;nbsp;are yet to be standardized or have their phytochemical content characterized.&amp;nbsp;&lt;strong&gt;Method: &lt;/strong&gt;This study identified the secondary metabolites in the stem bark&amp;nbsp;methanolic extract and quantified them. The same extract was subjected&amp;nbsp;to serial solvent fractionation, TLC characterization and antidiabetic testing.&amp;nbsp;&lt;strong&gt;Results: &lt;/strong&gt;The secondary metabolites were found to comprise of 7.5% alkaloids,&amp;nbsp;10% flavonoids, 13% tannins and 17% saponins per gram of plant material.&amp;nbsp;The TLC characteristics of the fractions (hexane (HX), ethylacetate (EA)&amp;nbsp;and methanol (ME)) viewed under UV light revealed spots with the following&amp;nbsp;Rf values; the hexane partition gave HX7EA3 (0.96 and 0.68) HX9EA1&amp;nbsp;(0.68 and 0.3), EA1ME9 (0.86 and 0.58), EA3ME7 (0.87), EA7ME3 (0.85)&amp;nbsp;and EA9ME1 (0.85). The ethylacetate partition gave the following HX1EA9 (0.53, 0.34 and 0.18), HX3EA7 (0.59, 0.40 and 0.26). &lt;strong&gt;Discussion: &lt;/strong&gt;All the&amp;nbsp;fractions produced nominal reduction of hyperglycemia. Except hexane&amp;nbsp;fraction at 50 mg/kg and ethylacetate fraction at 200 mg/kg all the fractions&amp;nbsp;had percentage reductions of glucose greater than that of the control at&amp;nbsp;the experimental doses. Although the values of percentage reductions of&amp;nbsp;hyperglycemia by the hexane fraction were apparently dose-dependent,&amp;nbsp;the greatest margin of reduction of hyperglycemia was observed in the&amp;nbsp;residual aqueous fraction. &lt;strong&gt;Conclusion: &lt;/strong&gt;It was found that SCE contains&amp;nbsp;valuable phytochemicals in appreciable quantities which are antidiabetic.&amp;nbsp;The residual aqueous fraction is the most potent antihyperglycemic of the&amp;nbsp;solvent fractions.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">243</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Tanayen Julius Kihdze&lt;sup&gt;1,3&lt;/sup&gt;, Ajayi Abayomi Mayowa&lt;sup&gt;2,3&lt;/sup&gt;, Oloro Joseph&lt;sup&gt;1,3&lt;/sup&gt;, Ezeonwumelu Joseph OC&lt;sup&gt;3&lt;/sup&gt;, Tanayen Grace Ghaife&lt;sup&gt;5&lt;/sup&gt;, Adzu Bulus&lt;sup&gt;3,4&lt;/sup&gt;, Arthur van Aerschot&lt;sup&gt;6&lt;/sup&gt;, Gert Laekeman&lt;sup&gt;6&lt;/sup&gt;, Agaba Amon Ganafa&lt;sup&gt;1&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology and Therapeutics, Mbarara University of Science and Technology, P.O. Box 1410 Mbarara, UGANDA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology and Therapeutics, University of Ibadan, Ibadan, NIGERIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Kampala International University, Complementary and Alternative Medicine Research (KIU-CAMRES) group.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;National Institute for Pharmaceutical Research and Development (NIPRD) PMB 21 Abuja, NIGERIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Medical Laboratory Sciences, Kampala International University Bushenyi, UGANDA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;KU Leuven&amp;ndash;University of Leuven, Department of Pharmaceutical and Pharmacological Sciences 3000 BELGIUM.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ramasamy Manikandan</style></author><author><style face="normal" font="default" size="100%">Arumugam Vijaya Anand</style></author><author><style face="normal" font="default" size="100%">Sampath Kumar</style></author><author><style face="normal" font="default" size="100%">Pushpa</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical and In vitro Antidiabetic Activity of Psidium Guajava Leaves</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alpha amylase</style></keyword><keyword><style  face="normal" font="default" size="100%">Alpha glucosidase</style></keyword><keyword><style  face="normal" font="default" size="100%">P. guajava</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June/2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">392-394</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; The present investigation includes the preliminary screening of phytochemicals and evaluation of &lt;em&gt;in vitro&lt;/em&gt; antidiabetic activity of &lt;em&gt;Psidium guajava&lt;/em&gt; leaves extracts. &lt;strong&gt;Materials&lt;/strong&gt; &lt;strong&gt;and Methods:&lt;/strong&gt; Plant material was subjected to the extraction preparation by soxhlet apparatus by using various solvents such as aqueous, ethanol, chloroform, petroleum ether and hexane. The various kinds of phytochemicals were detected and then &lt;em&gt;in vitro&lt;/em&gt; antidiabetic activity of &lt;em&gt;P. guajava &lt;/em&gt;were detected by using alpha amylase and alpha glucosidase enzyme in an &lt;em&gt;in vitro&lt;/em&gt; model. &lt;strong&gt;Results:&lt;/strong&gt; The study reveals the presence of phytochemicals such as carbohydrate, tannin, flavonoids, phenols etc., Among the various extracts the aqueous and ethanolic extracts which contains the large number of phytoconstituents. The &lt;em&gt;P. guajava &lt;/em&gt;leaves has been successfully inhibited both the enzymes in an &lt;em&gt;in vitro&lt;/em&gt; model. The aqueous extracts of &lt;em&gt;P. guajava&lt;/em&gt; leaves inhibited the alpha amylase and alpha glucosidase enzymes as 72.1% and 74.8% respectively. The ethanolic extract of &lt;em&gt;P. guajava &lt;/em&gt;leaves inhibited the alpha amylase and alpha glucosidase enzymes as 97.5% and 91.8% respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; From the results obtained in the current studies, the &lt;em&gt;P. guajava &lt;/em&gt;leaves have a prominent antidiabetic property in an &lt;em&gt;in vitro&lt;/em&gt; model and further studies can be carried out in an &lt;em&gt;in vivo&lt;/em&gt; model and the isolation of activie compound from&lt;em&gt; P. guajava &lt;/em&gt;leaves extract is needed&lt;em&gt;.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">392</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ramasamy Manikandan&lt;sup&gt;1&lt;/sup&gt;, Arumugam Vijaya Anand&lt;sup&gt;2&lt;/sup&gt;, Sampath Kumar&lt;sup&gt;3&lt;/sup&gt; and Pushpa&lt;sup&gt;4 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of BioChemistry, M.I.E.T Arts and Science College, Trichirappalli-620 007, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Human Genetics and Molecular Biology, Bharathiar University, Coimbatore-641 046, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Chemistry and Biosciences, SASTRA University, Kumbakonam&amp;ndash;612 001, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Microbiology, Cauvery College for Women, Tiruchirappalli&amp;ndash;620 018, Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vijaya Anand</style></author><author><style face="normal" font="default" size="100%">Manikandan</style></author><author><style face="normal" font="default" size="100%">Vijaya Kumar</style></author><author><style face="normal" font="default" size="100%">Sampath Kumar</style></author><author><style face="normal" font="default" size="100%">Pushpa</style></author><author><style face="normal" font="default" size="100%">Agaath Hedina</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytopharmacological overview of Psidium guajava Linn.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anticancer.</style></keyword><keyword><style  face="normal" font="default" size="100%">Antidiabetic</style></keyword><keyword><style  face="normal" font="default" size="100%">Antimicrobial</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatoprotective</style></keyword><keyword><style  face="normal" font="default" size="100%">Psidium guajava</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June/2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">314-320</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;em&gt;Psidium guajava &lt;/em&gt;Linn. possesses useful medicinal benefits. It has been recognized as the medicinally essential phytoconstituents, such as phenolic, flavonoid and carotenoid. Numerous pharmacological investigation have confirmed that the ability of this plant is to exhibit antimicrobial, antidiabetic, cardioprotective, neuroprotective, hepatoprotective, antioxidant and anticancer activities and it supports the traditional uses. This is a comprehensive of the phytoconstituents and pharmacological benefits.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">314</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Vijaya Anand&lt;sup&gt;1&lt;/sup&gt;, Manikandan&lt;sup&gt;2&lt;/sup&gt;, Vijaya Kumar&lt;sup&gt;2&lt;/sup&gt;, Sampath Kumar&lt;sup&gt;3&lt;/sup&gt;, Pushpa&lt;sup&gt;4&lt;/sup&gt;, Agaath Hedina&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Human Genetics and Molecular Biology, Bharatiar University, Coimbatore-641 046, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biochemistry, M.I.E.T. Arts and Science College,Tiruchirappalli-620 007, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Chemistry and Biosciences, SASTRA University, Kumbakonam-612 001, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Microbiology, Cauvery College for Women, Tiruchirappalli-620 018,Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Agaath Hedina</style></author><author><style face="normal" font="default" size="100%">Punniya Kotti</style></author><author><style face="normal" font="default" size="100%">Juveriyah Kausar</style></author><author><style face="normal" font="default" size="100%">Sivasamy</style></author><author><style face="normal" font="default" size="100%">Vijaya Anand</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytopharmacological overview of Terminalia chebula Retz</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-arthritic</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-carcinogenic</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-fungal</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-inflammatory.</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-oxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Free radical</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytoconstituents</style></keyword><keyword><style  face="normal" font="default" size="100%">Renoprotective</style></keyword><keyword><style  face="normal" font="default" size="100%">Terminalia chebula</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June/2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">307-309</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;Phytotherapy is the traditional method used to cure many diseases. Various medicinal plants found in many parts of India are well known for their various medicinal values. The &lt;em&gt;Terminalia chebula&lt;/em&gt; Retz. a native plant of Asia is found to have various properties like anti-oxidant and free radical scavenging activity, anti-carcinogenic activity, ant-imutagenic activity, anti-bacterial activity, anti-fungal activity, anti-viral activity, anti-diabetic, renoprotective activity, cardio-protective activity, anti-inflammatory and anti-arthritic activity. These properties of &lt;em&gt;T. chebula&lt;/em&gt; discussed in this review are mainly due to the presence of various types of phytoconstituents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">307</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Agaath Hedina&lt;sup&gt;1&lt;/sup&gt;, Punniya Kotti&lt;sup&gt;2&lt;/sup&gt;, Juveriyah Kausar&lt;sup&gt;1&lt;/sup&gt;, Sivasamy&lt;sup&gt;1&lt;/sup&gt;, Vijaya Anand&lt;sup&gt;1&lt;/sup&gt;* &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Human Genetics and Molecular Biology, Bharathiar University, Coimbatore, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biochemistry, Kanchi Shri Krishna College of Arts and Science, Kancheepuram, Tamil Nadu, INDIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Reena Kulkarni</style></author><author><style face="normal" font="default" size="100%">Suhas Kumar Shetty</style></author><author><style face="normal" font="default" size="100%">Rajarajeshwari N M</style></author><author><style face="normal" font="default" size="100%">Prasanna Narasimha Rao</style></author><author><style face="normal" font="default" size="100%">Nayan J</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Rasayana Herbs of Ayurveda to Treat age Related Cognitive Decline: An Update</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ayurveda</style></keyword><keyword><style  face="normal" font="default" size="100%">cognitive decline</style></keyword><keyword><style  face="normal" font="default" size="100%">Dementia</style></keyword><keyword><style  face="normal" font="default" size="100%">Herbs</style></keyword><keyword><style  face="normal" font="default" size="100%">Medhya</style></keyword><keyword><style  face="normal" font="default" size="100%">Rasayana.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Oct 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">411-423</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Cognitive decline associated with aging could be minor or major neuro-cognitive disorder presenting with progressive intellectual deterioration interfering with day to day activities. Behaviour and personality changes may complicate the life in due course. Significant increase in global prevalence of people aged above 60 years has raised concerns on effective management of old age problems. Age related cognitive deficits and dementia raise to the level of epidemics and established management is yet underway. Principles of preventive health and rasayana (rejuvenative) herbs of Ayurveda are being extensively researched up on for their effectiveness in dementia. In this fourteen such herbs with anti dementia property are discussed with relevant research update. &lt;strong&gt;Methods:&lt;/strong&gt; Herbs like amalaki (&lt;em&gt;Emblica officinalis&lt;/em&gt;), hareetaki (&lt;em&gt;Terminalia chebula&lt;/em&gt;), haridra (&lt;em&gt;Curcuma longa&lt;/em&gt;), manduka parni (&lt;em&gt;Centella asiatica&lt;/em&gt;), aindri (&lt;em&gt;Bacopa monniera&lt;/em&gt;), yastimadhu (&lt;em&gt;Glycirrhiza glabra&lt;/em&gt;), guduchi (&lt;em&gt;Tinospora cordifolia&lt;/em&gt;), shankhapushpi (&lt;em&gt;Convolvulus pleuricaulis&lt;/em&gt;), vacha (&lt;em&gt;Acorus calamus&lt;/em&gt;), jyotishmati (&lt;em&gt;Celastrus panniculata&lt;/em&gt;), kushmanda (&lt;em&gt;Benincasa hispida&lt;/em&gt;), Jatamamsi (&lt;em&gt;Nardostachys jatamamsi&lt;/em&gt;), ashvagandha (&lt;em&gt;Withania somnifera&lt;/em&gt;) and kapikacchu (&lt;em&gt;Mucuna pruriens&lt;/em&gt; (&lt;em&gt;Linn&lt;/em&gt;.)) are already proven of their efficacy in experimental and preclinical levels. The contents and research evidences are collected from ayurveda database on medicinal plants used in Ayurveda and Siddha and other authentic literature, Google scholar, Science direct, online and print journals. &lt;strong&gt;Discussion:&lt;/strong&gt; The herbs in discussion mostly act on reactive oxygen species and oxidative stress injury by antioxidant properties and neuroprotective activity. Acetylcholine esterase inhibition, N-Methyl-D-Aspartate antagonism, Dopaminergic activity, Anti-amyloidogenic activity, Inhibition of Tau aggregation, neuroprotection and immune modulation are activity path ways. Tridosha namely Kapha, Pitta and Vata may be viewed to be categorically predominant in initial, middle and final stage of dementia. Selected herbs thus can be specific based on the pathology and relevant dosha predominance.&lt;strong&gt; Conclusion: &lt;/strong&gt;Rasayana herbs with current updates and inferences can serve as an eye-opener for further researches at molecular and clinical aspect.&lt;/p&gt;

</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">411</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Reena Kulkarni&lt;sup&gt;1*&lt;/sup&gt;, Suhas Kumar Shetty&lt;sup&gt;2&lt;/sup&gt;, Rajarajeshwari N M&lt;sup&gt;3&lt;/sup&gt;, Prasanna Narasimha Rao&lt;sup&gt;4&lt;/sup&gt; and Nayan J&lt;sup&gt;5 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Kaumarabhritya, SDM College of Ayurveda, Tanniruhalla, Hassan-INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Manasa Roga, SDM College of Ayurveda, Tanniruhalla, Hassan-INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Samhita and Siddhanta, SDM College of Ayurveda, Tanniruhalla, Hassan-INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Shalya Tantra, SDM College of Ayurveda, Tanniruhalla, Hassan-INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Agada tantra, Sri Kalabairaveshvara Swamy Ayurveda Medical College, RPC layout, Vijayanagar, Bengaluru-40, Karnataka, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Juveriyah Kausar</style></author><author><style face="normal" font="default" size="100%">Durai Muthumani</style></author><author><style face="normal" font="default" size="100%">Agaath Hedina</style></author><author><style face="normal" font="default" size="100%">Sivasamy</style></author><author><style face="normal" font="default" size="100%">Vijaya Anand</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Review of the phytochemical and pharmacological activities of Euphorbia hirta Linn.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anti-apoptotic.</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-bacterial</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-oxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Diuretic</style></keyword><keyword><style  face="normal" font="default" size="100%">Euphorbia hirta</style></keyword><keyword><style  face="normal" font="default" size="100%">Sedative</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June/2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">310-313</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;The use of plant extract to cure diseases has been the traditional way used in many parts of the world. The synthetic drugs used now are more prone to cause side effects than curing the disease. Hence, the use of plant extract has now emerged due to their effective action against the disease without causing any side effects. The plants belonging to the family called Euphorbia are widely used in medicine for its wide medicinal properties. The plant &lt;em&gt;Euphorbia hirta&lt;/em&gt; has properties like anti-bacterial, anti-diarrheal, anti-allergic, diuretic, anti-oxidant, anti-tumor, anti-diabetic, anxiolytic and sedative activity. This review contains the detailed information about all the properties of &lt;em&gt;E. hirta.&lt;/em&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">310</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Juveriyah Kausar &lt;sup&gt;1&lt;/sup&gt;, Durai Muthumani &lt;sup&gt;2&lt;/sup&gt;, Agaath Hedina &lt;sup&gt;1&lt;/sup&gt;, Sivasamy &lt;sup&gt;1&lt;/sup&gt;, Vijaya Anand &lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Human Genetics and Molecular Biology, Bharatiar University, Coimbatore &amp;ndash; 641 046, Tamil Nadu, INDIA.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biochemistry, Kanchi Shri Krishna College of Arts and Science, Kilambi,&amp;nbsp;Kancheepuram &amp;ndash; 631 551, Tamil Nadu, INDIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Abirami Hariharan</style></author><author><style face="normal" font="default" size="100%">Tajuddin Nargis Begum</style></author><author><style face="normal" font="default" size="100%">Mohamed Hussain Muhammad Ilyas</style></author><author><style face="normal" font="default" size="100%">Hussain Syed Jahangir</style></author><author><style face="normal" font="default" size="100%">Premkumar Kumpati</style></author><author><style face="normal" font="default" size="100%">Shilu Mathew</style></author><author><style face="normal" font="default" size="100%">Archunan Govindaraju</style></author><author><style face="normal" font="default" size="100%">Ishtiaq Qadri</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis of Plant Mediated gold Nanoparticles using Azima Tetracantha Lam. Leaves extract and Evaluation of their Antimicrobial Activities</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimicrobial Activity.</style></keyword><keyword><style  face="normal" font="default" size="100%">Azima tetracantha Leaves Extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Biosynthesis</style></keyword><keyword><style  face="normal" font="default" size="100%">Characterization</style></keyword><keyword><style  face="normal" font="default" size="100%">Gold Nanoparticles</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Oct 2016</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">507-512</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Aim: &lt;/strong&gt;The demand for nanoparticles is increasing day by day due to their wide range of applications in various areas including pharmaceutical industry. Nanoparticles are formally synthesized by chemical methods in which the toxic and flammable chemicals are used. &lt;strong&gt;Methods: &lt;/strong&gt;This article reports about an effective, rapid and eco-friendly technique for the fabrication of gold nanoparticles from gold chloride solution using &lt;em&gt;Azima tetracantha&lt;/em&gt; Lam. leaves extract. The effects of the leaves extract of &lt;em&gt;Azima tetracantha&lt;/em&gt;, the concentration of Gold chloride solution, the time of the reaction and the effect of tem&amp;not;perature on the rate of the reaction were investigated. The synthesized gold nanoparticles (AuNPs) were characterized by using various techniques such as Dynamic Light Spectroscopy (DLS), Scanning Electron Microscopy (SEM), UV-Vis spectra gave surface plasmon resonance (SPR) at 540 nm, Fourier Transform Infrared spectroscopy (FTIR) and X-ray diffraction (XRD). This revealed the reduction of gold ions (Au&lt;sup&gt;+&lt;/sup&gt;) to gold metal (Au&lt;sup&gt;0&lt;/sup&gt;) which indicated the formation of gold nanoparticles (AuNPs). &lt;strong&gt;Results:&lt;/strong&gt; The antimicrobial action of biosynthesized AuNPs indicated effective activity against bacterial pathogens &lt;em&gt;Aeromonas liquefaciens&lt;/em&gt;, &lt;em&gt;Enterococcus fecalis&lt;/em&gt;, &lt;em&gt;Micrococcus luteus&lt;/em&gt;, &lt;em&gt;Salmonella typhimurium&lt;/em&gt; and fungal pathogens &lt;em&gt;Candida albicans&lt;/em&gt;, &lt;em&gt;Cryptococcus sp, Microsporum canis, Trichophyton rubrum&lt;/em&gt;.&lt;strong&gt; Conclusion:&lt;/strong&gt; This revealed that gold nanoparticles could provide a safer alternative to conventional antimicrobial agents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">507</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Abirami Hariharan&lt;sup&gt;1&lt;/sup&gt;, Tajuddin Nargis Begum&lt;sup&gt;2&lt;/sup&gt;, Mohamed Hussain Muhammad Ilyas&lt;sup&gt;3&lt;/sup&gt;, Hussain Syed Jahangir&lt;sup&gt;3&lt;/sup&gt;, Premkumar Kumpati&lt;sup&gt;4&lt;/sup&gt;, Shilu Mathew&lt;sup&gt;2&lt;/sup&gt;, Archunan Govindaraju&lt;sup&gt;5&lt;/sup&gt;, and Ishtiaq Qadri&lt;sup&gt;6*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;1Department of Biotechnology, Cauvery College for Women, Trichy- 18, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biotechnology, Jamal Mohamed College (Autonomous), Trichy-20, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Botany, Jamal Mohamed College (Autonomous), Trichy-20, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Biomedical Sciences, Bharathidasan University, Trichy-24, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Animal Science, Center for Pheromone Technology, Bharathidasan University Tiruchirappalli-620 024, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;6&lt;/sup&gt;King Fahad Medical Research Centre, King Abdul Aziz University, Jeddah, SAUDI ARABIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rajagopal Ramasubramania raja</style></author><author><style face="normal" font="default" size="100%">Koumara Velou Kailasam</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Abutilon indicum L (Malvaceae)-Medicinal Potential Review</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Abutilon indicum</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti asthmatic</style></keyword><keyword><style  face="normal" font="default" size="100%">Anti-proliferative activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatoprotective activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolic compounds</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Nov-Dec 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">330-332</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;The plant Abutilon Indicum (Linn.) is belonging to malvaceae family; Also known as Mallow in english, Abutilon indicum is used as a medicinal plant. It has been reported that Abutilon indicum has Anti inflammatory and Antiproliferative activity, Anti-Arthritic activity, Analgesic and Sedative property, Antioxidant and Antimicrobial activity, Hepatoprotective activity, Anti diabetic, Anti cancer, Anti diarrhoeal, Anti-convulsant, Larvicidal, Wound healing, Anti asthmatic, Diuretic, Immunomodulatory, and Anti-estrogenic activity. It is proved that this plant contains carbohydrates, proteins and aminio acids, saponins, flavanoids, glycosides, phytosterols and phenolic compounds&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">330</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Rajagopa&lt;sup&gt;l&lt;/sup&gt; Ramasubramania raja&lt;sup&gt;*1&lt;/sup&gt; and Koumara Velou Kailasam&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacy, Research Scholar PRIST University, Thanjavur, T.N, India. 2Registrar, PRIST University, Thanjavur, T.N, India&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vijay Kumar Matta</style></author><author><style face="normal" font="default" size="100%">Praveen Kumar Pasala</style></author><author><style face="normal" font="default" size="100%">Silvia Netala</style></author><author><style face="normal" font="default" size="100%">Satish Pandrinki</style></author><author><style face="normal" font="default" size="100%">Prasad Konduri</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anti Hypertensive Activity of the Ethanolic Extract of Lantana camara leaves on high salt loaded wistar albino rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">EELC (Ethanolic extract of Lantana camara leaves)</style></keyword><keyword><style  face="normal" font="default" size="100%">Hypertension</style></keyword><keyword><style  face="normal" font="default" size="100%">Mean arterial blood pressure (MABP) and Normotensive rats (NTR).</style></keyword><keyword><style  face="normal" font="default" size="100%">Wistar albino rats</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">01/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">289-295</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Hypertension is the most common and major cardiovascular disease. There is an urgent need for treament of hypertension by exploration of several medicinal plants having potent anti hypertensive activity as the modern medicines are having many side effects. &lt;strong&gt;Objective:&lt;/strong&gt; The study focus on scientific evaluation of antihypertensive activity of ethanolic extract of &lt;em&gt;Lantana camara&lt;/em&gt; leaves (EELC) in different experimental models. &lt;strong&gt;Material &amp;amp; methods:&lt;/strong&gt; Antihypertensive activity was conducted on wister albino rats by determining serum glutamic oxaloacetic transaminase (SGOT), serum glutamic pyruvic transaminase (SGPT), creatinine and Sodium levels by using Semi Autoanalyser and Flame photometer; chick mean arterial blood pressure by using condon&amp;rsquo;s mercury manometer and isolated frog heart for recording cardic responses using student kymograph. &lt;strong&gt;Results:&lt;/strong&gt; EELC produced negative inotropic and negative chronotropic effect, antagonised by atropine on isolated frog heart. EELC shows dose dependent (p&amp;lt;0.05) decreased mean arterial blood pressure (MABP) in anaesthetic chick. Salt treated rats displayed significant (p&amp;lt;0.05) increase in blood level of SGOT, SGPT, Creatinine and sodium, decrease in pottassim levels in comparision with normal rats. Treatment with EELC (200 and 400 mg/kg) significantly balanced the ionic levels such as lower the sodium and elevate the potassium levels. Creatinine levels were signifi-cantly (p&amp;lt;0.05) reduced by the treatment with EELC. There are no significant changes occurred in serum SGOT and SGPT upon EELC administration. The present study suggests that treatment of salt hypertensive rats with EELC protects against renal injuries.&lt;strong&gt; Conclusion:&lt;/strong&gt; It was concluded that ethanolic extract of &lt;em&gt;Lantana camara&lt;/em&gt; leaves reduces work load of heart, maintain inotonic levels by negative chronotropic effect, relaxes the smooth muscles in chick and salt hypertensive rats against renal and vascular injuries is proved.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">289</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Vijay Kumar Matta, Praveen Kumar Pasala&lt;sup&gt;*&lt;/sup&gt;, Silvia Netala, Satish Pandrinki and Prasad Konduri &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Pharmacology, Shri Vishnu College of Pharmacy, Bhimavaram, Andhra Pradesh, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nahid Mahmoud Hassan El-Ameen</style></author><author><style face="normal" font="default" size="100%">Manal Mohamed Elhassan Taha</style></author><author><style face="normal" font="default" size="100%">Siddig Ibrahim Abdelwahab</style></author><author><style face="normal" font="default" size="100%">Asaad Khalid</style></author><author><style face="normal" font="default" size="100%">Fatima Elfatih</style></author><author><style face="normal" font="default" size="100%">Mona Awad Kamel</style></author><author><style face="normal" font="default" size="100%">Bassem Yousif Sheikh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anti-diabetic Properties of Thymoquinone is unassociated with Glycogen Phosphorylase Inhibition</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Diabetes</style></keyword><keyword><style  face="normal" font="default" size="100%">Docking</style></keyword><keyword><style  face="normal" font="default" size="100%">Enzyme</style></keyword><keyword><style  face="normal" font="default" size="100%">Glycogen phosphorylase inhibition</style></keyword><keyword><style  face="normal" font="default" size="100%">Streptozotocin</style></keyword><keyword><style  face="normal" font="default" size="100%">Thymoquinone.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">01/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">406-410</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Nigella sativa&lt;/em&gt; L. (Black seed), is commonly used by traditional healers as a remedy for more than four thousand years. The antidiabetic property of &lt;em&gt;N. sativa&lt;/em&gt; seeds oil is attributable to the presence of Thymoquinone (TQ). On the other hand many studies have been designed to investigate the possible effects of the TQ in Streptozotocin (STZ) and nicotinamide (NA)-induced diabetes in rats. &lt;strong&gt;Aim of the study: &lt;/strong&gt;The aim of this study was to elucidate the mechanisms underlying the glucose lowering effects of thymoquinone. &lt;strong&gt;Methods:&lt;/strong&gt; &lt;em&gt;In vitro&lt;/em&gt; and &lt;em&gt;in silico&lt;/em&gt; using glycogen phosphorylase (GPa) enzyme assay and docking tools were used. &lt;strong&gt;Results:&lt;/strong&gt; Oral administration of TQ for 60 days, dose dependently improved the glycemic status in STZ-NA induced diabetic rats. GPa activity was measured in the direction of glycogen synthesis by the release of phosphate from glucose-1-phosphate. TQ at a concentration of 0.05 Mm inhibits GPa activity by only 14.9%. &lt;strong&gt;Conclusion:&lt;/strong&gt; These results show that TQ at 60 mg/kg b.w is associated with potential antihyperglycemic effects. Furthermore, anti-diabetic properties of TQ are unassociated with glycogen phosphorylase inhibition.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">406</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Nahid Mahmoud Hassan El-Ameen&lt;sup&gt;1*&lt;/sup&gt;, Manal Mohamed Elhassan Taha&lt;sup&gt;1*&lt;/sup&gt;, Siddig Ibrahim Abdelwahab&lt;sup&gt;1&lt;/sup&gt;, Asaad Khalid&lt;sup&gt;1&lt;/sup&gt;, Fatima Elfatih&lt;sup&gt;2&lt;/sup&gt;, Mona Awad Kamel&lt;sup&gt;1&lt;/sup&gt; and Bassem Yousif Sheikh&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biomedical Research Unit, Researcher at Medical Research Center, Jazan University, Jazan, Saudi Arabia.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Biochemistry Medicinal and Aromatic Plants Research Institute, National Centre for Research, P. O. Box 2420 Khartoum, Sudan.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Surgery, MABL Chair, College of Medicine, Taibah University, Saudi Arabia.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bassem Yousef Sheikh</style></author><author><style face="normal" font="default" size="100%">Manal Mohamed Elhassan Taha</style></author><author><style face="normal" font="default" size="100%">Waleed Syaed Koko</style></author><author><style face="normal" font="default" size="100%">Siddig Ibrahim Abdelwahab</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antimicrobial Effects of Thymoquinone on Entamoeba histolytica and Giardia lamblia</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Entamoeba histolytica</style></keyword><keyword><style  face="normal" font="default" size="100%">Giardia lamblia.</style></keyword><keyword><style  face="normal" font="default" size="100%">Nigella sativa</style></keyword><keyword><style  face="normal" font="default" size="100%">Prophetic Medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Thymoquinone</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">December 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><pages><style face="normal" font="default" size="100%">168-170</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background&lt;/strong&gt;: Parasitic infections are a major difficulty in tropical and subtropical countries. Traditionally medicinal plants have been used in folk medicine to treat parasitic infections and are a valuable source of novel anti-parasitics. &lt;strong&gt;Objective: &lt;/strong&gt;In our search for therapeutic alternatives to anti- protozoal chemotherapy, thymoquinone, the active ingredient of Black cumin (Nigella sativa) was examined. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Thymoquinone was tested against Entamoeba histolytica and Giardia lamblia using in vitro susceptibility assays and the mortality of the parasites were then obtained using the standard calculations. The compound was also tested for 48 and 72 hours on both parasites. &lt;strong&gt;Results:&lt;/strong&gt; The current study indicate that the mortality of TQ showed 85.5%, 91.5% and 96.8% mortality on E. histolytica for 25 ppm at 24 hr, 48 and 72 hr, respectively, with IC50 2&amp;yen;10-19,. On the other hand, this natural compound showed a mortality of 82.83%, 91.76% and 96.62% mortality on G. lamblia for 25 ppm at 24 hr, 48 and 72 hr, respectively, with IC50 4.8&amp;yen;10-5. Metrondizole powder gave 70.9% mortality at 156 ppm at the same times.&lt;strong&gt; Conclusion:&lt;/strong&gt; The current results indicate that TQ is more potent on E. histolytica compared to G. lamblia. Further pharmacological studies were needed to help in the clinical presentation of thymoquinone.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">168</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Bassem Yousef Sheikh&lt;sup&gt;1&lt;/sup&gt;, Manal Mohamed Elhassan Taha&lt;sup&gt;2,&lt;/sup&gt; Waleed Syaed Koko&lt;sup&gt;3&lt;/sup&gt;, and Siddig Ibrahim Abdelwahab&lt;sup&gt;3&lt;/sup&gt;*&lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Al-Moalim MA Bin Ladin (MABL) chair for Scientific Miracles of Prophetic Medicine, College of Medicine, Taibah University, SAUDI ARABIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Unit of Biomedical Research, Medical Research Centre, Jazan University, P.O. Box 114 Jazan, Jazan 45142, SAUDI ARABIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Microbiology, Medicinal and Aromatic Research Institute, National Research Centre, Khartoum, SAUDI ARABIA. 4Unit of Biomedical Research, Substance Abuse Research Centre, Jazan University, P.O. Box 114 Jazan, Jazan 45142, SAUDI ARABIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Girindrababu Venkattappa Jayashree</style></author><author><style face="normal" font="default" size="100%">Puttasiddiah Rachitha</style></author><author><style face="normal" font="default" size="100%">Krishnaswamy Krupashree</style></author><author><style face="normal" font="default" size="100%">Kandikattu Hemanth Kumar</style></author><author><style face="normal" font="default" size="100%">Farhath Khanum</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antioxidant and DNA Damage Protective Effects of Asparagus racemosus in Human Colon and Mice Muscle Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">AAPH</style></keyword><keyword><style  face="normal" font="default" size="100%">Asparagus racemosus</style></keyword><keyword><style  face="normal" font="default" size="100%">C2C12</style></keyword><keyword><style  face="normal" font="default" size="100%">HT29</style></keyword><keyword><style  face="normal" font="default" size="100%">Protein oxidation</style></keyword><keyword><style  face="normal" font="default" size="100%">Single cell gel electrophoresis.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">01/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">182-190</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The present study was designed to investigate the &lt;em&gt;in vitro&lt;/em&gt; antioxidant and macromolecule damage protective effects of &lt;em&gt;Asparagus racemosus&lt;/em&gt; water (AWE) and methanolic (AME) fractions of roots. &lt;strong&gt;Methods:&lt;/strong&gt; The &lt;em&gt;in vitro&lt;/em&gt; antioxidant activity of AWE/AME was estimated by free radical scavenging assays. The DNA damage of HT29 and C2C12 cells was analyzed by comet assay. The plasmid DNA damage and protein oxidation were carried out by agarose gel electrophoresis and SDS-PAGE analysis respectively, where as lipid peroxidation was performed by TBARS assay. &lt;strong&gt;Results:&lt;/strong&gt; Both the extracts showed scavenging activity with IC&lt;sub&gt;50&lt;/sub&gt; values of 417.4 &amp;plusmn; 19.5 / 298 &amp;plusmn; 13.5, 381 &amp;plusmn; 18.2 / 235 &amp;plusmn; 11.9, 54.8 &amp;plusmn; 2.95 / 31.6 &amp;plusmn; 1.52, 28.9 &amp;plusmn; 1.73 / 19.7 &amp;plusmn; 1.55 &amp;mu;g/mL for DPPH, metal chelating, ABTS and Nitric oxide scavenging activities respectively. Similarly the methanolic extract showed more potent reducing power and total antioxidant activities over water fraction. The AME showed 56.8% and 41.2% protection against H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; (Hydrogen peroxide) induced DNA damage of HT29 human colon cells and C2C12 murine myoblasts. The extract also showed protection against H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; induced plasmid DNA damge, AAPH induced protein oxidation of bovine serum albumin (BSA) and lipid peroxidation of rat hepatic tissue. &lt;strong&gt;Conclusion: &lt;/strong&gt;Over all this study showed remarkable antioxidant and macromolecule damage protective effects of &lt;em&gt;A. racemosus.&lt;/em&gt; The observed biological properties may be attributed to the high content phenols and flavonoids in the methanolic extract &lt;em&gt;A. racemosus&lt;/em&gt; over water extract.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">182</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Girindrababu Venkattappa Jayashree, Puttasiddiah Rachitha, Krishnaswamy Krupashree, Kandikattu Hemanth Kumar, Farhath Khanum&lt;sup&gt;*&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Biochemistry and Nanosciences discipline, Defence food research laboratory, Siddartha Nagar, Mysore, Karnataka-570 011, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Girindrababu Venkattappa Jayashree</style></author><author><style face="normal" font="default" size="100%">Puttasiddiah Rachitha</style></author><author><style face="normal" font="default" size="100%">Krishnaswamy Krupashree</style></author><author><style face="normal" font="default" size="100%">Kandikattu Hemanth Kumar</style></author><author><style face="normal" font="default" size="100%">Farhath Khanum</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antioxidant and DNA Damage Protective Effects of Asparagus racemosus in Human Colon and Mice Muscle Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">AAPH</style></keyword><keyword><style  face="normal" font="default" size="100%">Asparagus racemosus</style></keyword><keyword><style  face="normal" font="default" size="100%">Protein oxidation</style></keyword><keyword><style  face="normal" font="default" size="100%">Single cell gel electrophoresis.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">9th Feb, 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">182-190</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The present study was designed to investigate the in vitro antioxidant and macromolecule damage protective effects of Asparagus racemosus water (AWE) and methanolic (AME) fractions of roots. &lt;strong&gt;Methods:&lt;/strong&gt; The in vitro antioxidant activity of AWE/AME was estimated by free radical scavenging assays. The DNA damage of HT29 and C2C12 cells was analyzed by comet assay. The plasmid DNA damage and protein oxidation were carried out by agarose gel electrophoresis and SDS-PAGE analysis respectively, where as lipid peroxidation was performed by TBARS assay. &lt;strong&gt;Results:&lt;/strong&gt; Both the extracts showed scavenging activity with IC&lt;sub&gt;50&lt;/sub&gt; values of 417.4 &amp;plusmn; 19.5 / 298 &amp;plusmn; 13.5, 381 &amp;plusmn; 18.2 / 235 &amp;plusmn; 11.9, 54.8 &amp;plusmn; 2.95 / 31.6 &amp;plusmn; 1.52, 28.9 &amp;plusmn; 1.73 / 19.7 &amp;plusmn; 1.55 &amp;mu;g/mL for DPPH, metal chelating, ABTS and Nitric oxide scavenging activities respectively. Similarly the methanolic extract showed more potent reducing power and total antioxidant activities over water fraction. The AME showed 56.8% and 41.2% protection against H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; (Hydrogen peroxide) induced DNA damage of HT29 human colon cells and C2C12 murine myoblasts. The extract also showed protection against H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; induced plasmid DNA damge, AAPH induced protein oxidation of bovine serum albumin (BSA) and lipid peroxidation of rat hepatic tissue. &lt;strong&gt;Conclusion: &lt;/strong&gt;Over all this study showed remarkable antioxidant and macromolecule damage protective effects of A.racemosus. The observed biological properties may be attributed to the high content phenols and flavonoids in the methanolic extract A. racemosus over water extract.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words: &lt;/strong&gt;AAPH, &lt;em&gt;Asparagus racemosus&lt;/em&gt;, C2C12, HT29, Protein oxidation, Single cell gel electrophoresis.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">182</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Girindrababu Venkattappa Jayashree, Puttasiddiah Rachitha, Krishnaswamy Krupashree, Kandikattu Hemanth Kumar, Farhath Khanum&lt;sup&gt;*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align:justify&quot;&gt;Department of Biochemistry and Nanosciences discipline, Defence food research laboratory, Siddartha Nagar, Mysore, Karnataka-570 011, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ravinder Kaur</style></author><author><style face="normal" font="default" size="100%">Sarabjit Kaur</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anxiolytic Potential of Methanol Extract from Ageratum conyzoides Linn Leaves</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ageratum conyzoides</style></keyword><keyword><style  face="normal" font="default" size="100%">Anxiolytic</style></keyword><keyword><style  face="normal" font="default" size="100%">Methanol extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercetin</style></keyword><keyword><style  face="normal" font="default" size="100%">TLC</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jul-Aug 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">236-241</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Objective:&lt;/strong&gt; Ageratum conyzoides Linn. (Asteraceae) has been widely used in African traditional medicine for healing mental and infectious diseases. The present study was designed to scientifically validate the traditional claim of A. conzyoides as anti-anxiety drug and to identify the compound responsible for the anxiolytic effects of A. conzyoides. &lt;strong&gt;Method:&lt;/strong&gt; The methanol extract of A. conzyoides was prepared by soxhlet apparatus. The methanol extract was fractionated into ethylacetate and butanol fractions by liquid-liquid partitioning method. Methanol extract (100 and 200 mg/kg; p.o.) and its prepared fractions (25 and 50 mg/kg; p.o.) were evaluated for anxiolytic activity in mice by using elevated plus maze (EPM) model. Thin layer chromatography studies were performed to identify the possible anxiolytic component. &lt;strong&gt;Results:&lt;/strong&gt; Methanol extract at both doses showed significant, when compared to vehicle control group, increase in time spent and number of entries in open arms of EPM confirming the anti-anxiety effects of A. conzyoides. Liquid-liquid partitioning of methanol extract gave two fractions (ethylacetate and butanol) which were administrated at 25 and 50 mg/kg doses to mice in EPM, respectively. Results showed that ethylacetate fraction was responsible for anxiolytic effects of methanol extract of A. conzyoides. The TLC studies were carried out for ethylacetate fraction and Quercetin was identified by comparing Rf values with the standard (Quercetin). &lt;strong&gt;Conclusion: &lt;/strong&gt;The present investigation revealed that the extract has significant anxiolytic effect. The flavonoid quercetin may be responsible for the observed anxiolytic effects of A. conyzoides.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">236</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Ravinder Kaur&lt;sup&gt;1&lt;/sup&gt; and Sarabjit Kaur&lt;sup&gt;1*&lt;/sup&gt; &lt;/strong&gt;Department of Pharmaceutical Sciences, Pharmacognosy and Phytochemistry Laboratory, Guru Nanak Dev University, Amritsar-143005, INDIA&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ravinder Kaur</style></author><author><style face="normal" font="default" size="100%">Sarabjit Kaur</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anxiolytic Potential of Methanol Extract from Ageratum conyzoides Linn Leaves</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ageratum conyzoides</style></keyword><keyword><style  face="normal" font="default" size="100%">Anxiolytic</style></keyword><keyword><style  face="normal" font="default" size="100%">Methanol extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercetin</style></keyword><keyword><style  face="normal" font="default" size="100%">TLC.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">29th Apr, 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">236-241</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective: &lt;/strong&gt;&lt;em&gt;Ageratum conyzoides&lt;/em&gt; Linn. (&lt;em&gt;Asteraceae&lt;/em&gt;) has been widely used in African traditional medicine for healing mental and infectious diseases. The present study was designed to scientifically validate the traditional claim of A. conzyoides as anti-anxiety drug and to identify the compound responsible for the anxiolytic effects of A. conzyoides.&lt;strong&gt; Method:&lt;/strong&gt; The methanol extract of A. conzyoides was prepared by soxhlet apparatus. The methanol extract was fractionated into ethylacetate and butanol fractions by liquid-liquid partitioning method. Methanol extract (100 and 200 mg/kg; p.o.) and its prepared fractions (25 and 50 mg/kg; p.o.) were evaluated for anxiolytic activity in mice by using elevated plus maze (EPM) model. Thin layer chromatography studies were performed to identify the possible anxiolytic component. &lt;strong&gt;Results: &lt;/strong&gt;Methanol extract at both doses showed significant, when compared to vehicle control group, increase in time spent and number of entries in open arms of EPM confirming the anti-anxiety effects of A. conzyoides. Liquid-liquid partitioning of methanol extract gave two fractions (ethylacetate and butanol) which were administrated at 25 and 50 mg/kg doses to mice in EPM, respectively. Results showed that ethylacetate fraction was responsible for anxiolytic effects of methanol extract of A. conzyoides. The TLC studies were carried out for ethylacetate fraction and Quercetin was identified by comparing R&lt;sub&gt;f&lt;/sub&gt; values with the standard (Quercetin). &lt;strong&gt;Conclusion: &lt;/strong&gt;The present investigation revealed that the extract has significant anxiolytic effect. The flavonoid quercetin may be responsible for the observed anxiolytic effects of A. conyzoides.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;em&gt;&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;Ageratum conyzoides&lt;/em&gt;, Anxiolytic, Methanol extract, Quercetin, TLC.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">236</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ravinder Kaur&lt;sup&gt;1&lt;/sup&gt; and Sarabjit Kaur&lt;sup&gt;1*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Pharmaceutical Sciences, Pharmacognosy and Phytochemistry Laboratory, Guru Nanak Dev University, Amritsar-143005, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Siddig Ibrahim Abdelwahab</style></author><author><style face="normal" font="default" size="100%">Rashad Bin Mohammed Alsanosy</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Syam Mohan</style></author><author><style face="normal" font="default" size="100%">Manal Moahmed Elhassan Taha</style></author></secondary-authors><tertiary-authors><author><style face="normal" font="default" size="100%">Hamed Karimian</style></author></tertiary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Assessment of Cytotoxicity of Smokeless Tobacco (Shammah) In Hepg2 and WRL68 Cells Line</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hepatotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">In vitro models</style></keyword><keyword><style  face="normal" font="default" size="100%">Saudi Arabia</style></keyword><keyword><style  face="normal" font="default" size="100%">Shammah</style></keyword><keyword><style  face="normal" font="default" size="100%">Smokeless tobacco</style></keyword><keyword><style  face="normal" font="default" size="100%">Substance Absue Research Centre</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jul-Aug 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">242-248</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Shammah is a traditional form of chewing tobacco [Smokeless tobacco, (ST)] that is commonly used in the Middle east specially Saudi Arabia (KSA), Yemen and Sudan. The cytotoxicity of Sudanese and Yemenis ST hexane and methanol extracts was evaluated using MTT assay. Annexin-V assay has been used to detect the induction of apoptosis. Luminescence based assay also been conducted to check the level of caspases enzyme. The involvement of cell cycle check point arrest has been performed using flow cytometry analysis. The current study found that ST has the capacity to induce cell toxicity in human liver cells. The inhibitory capacity of ST in HepG2 and WRL 68 has been found to be 151 &amp;plusmn; 2.5 and 305 &amp;plusmn; 11.5 &amp;mu;g/ml for 24 h. An early apoptosis induction in HepG2 cells was observed by annexin V assay, which clearly exhibited significantly increased early and late apoptosis phases both at 24 and 48 h. Both the caspases-8 and-9 level was found to be increased by the introduction of ST to HepG2 cells significantly (p&amp;lt;0.05). Moreover the ST extract was able to arrest the cell cycle check point at G2/M phase. A significantly increasing pattern of hypodiploid phases of cells also been observed, which confirm the apoptosis induction again. Collectively, results presented in this study demonstrated that the ST, which is used as a euphoritic substance of abuse also, has significant level of toxicity in human cells. Moreover the mode of cell death was found to be though programmed cell death which is closely associated with cell cycle arrest&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">242</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Siddig Ibrahim Abdelwahab&lt;sup&gt;*1&lt;/sup&gt;, Syam Mohan&lt;sup&gt;2&lt;/sup&gt;, Manal Moahmed Elhassan Taha&lt;sup&gt;2&lt;/sup&gt;, Rashad Bin Mohammed Alsanosy&lt;sup&gt;1&lt;/sup&gt; and Hamed Karimian&lt;sup&gt;3&lt;/sup&gt;&lt;/strong&gt; &lt;sup&gt;1&lt;/sup&gt;Substance Abuse Research Centre, Jazan University, 11420, Jazan, Saudi Arabia 2Medical Research Center, Jazan University, 11420, Jazan, Saudi Arabia 3Department of Pharmacy, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Siddig Ibrahim Abdelwahab</style></author><author><style face="normal" font="default" size="100%">Syam Mohan,</style></author><author><style face="normal" font="default" size="100%">Manal Moahmed Elhassan Taha</style></author><author><style face="normal" font="default" size="100%">Rashad Bin Mohammed Alsanosy</style></author><author><style face="normal" font="default" size="100%">Hamed Karimian</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Assessment of Cytotoxicity of Smokeless Tobacco (Shammah) In Hepg2 and WRL68 Cells Line</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hepatotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">In vitro models</style></keyword><keyword><style  face="normal" font="default" size="100%">Saudi Arabia</style></keyword><keyword><style  face="normal" font="default" size="100%">Shammah.</style></keyword><keyword><style  face="normal" font="default" size="100%">Smokeless tobacco</style></keyword><keyword><style  face="normal" font="default" size="100%">Substance Absue Research Centre</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">29th Apr, 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">242-248</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;Shammah is a traditional form of chewing tobacco [Smokeless tobacco, (ST)] that is commonly used in the Middle east specially Saudi Arabia (KSA), Yemen and Sudan. The cytotoxicity of Sudanese and Yemenis ST hexane and methanol extracts was evaluated using MTT assay. Annexin-V assay has been used to detect the induction of apoptosis. Luminescence based assay also been conducted to check the level of caspases enzyme. The involvement of cell cycle check point arrest has been performed using flow cytometry analysis. The current study found that ST has the capacity to induce cell toxicity in human liver cells. The inhibitory capacity of ST in HepG2 and WRL 68 has been found to be 151 &amp;plusmn; 2.5 and 305 &amp;plusmn; 11.5 &amp;mu;g/ml for 24 h. An early apoptosis induction in HepG2 cells was observed by annexin V assay, which clearly exhibited significantly increased early and late apoptosis phases both at 24 and 48 h. Both the caspases-8 and-9 level was found to be increased by the introduction of ST to HepG2 cells significantly (p&amp;lt;0.05). Moreover the ST extract was able to arrest the cell cycle check point at G2/M phase. A significantly increasing pattern of hypodiploid phases of cells also been observed, which confirm the apoptosis induction again. Collectively, results presented in this study demonstrated that the ST, which is used as a euphoritic substance of abuse also, has significant level of toxicity in human cells. Moreover the mode of cell death was found to be though programmed cell death which is closely associated with cell cycle arrest.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words: &lt;/strong&gt;Hepatotoxicity,&lt;em&gt; In vitro&lt;/em&gt; models, Saudi Arabia, Smokeless tobacco, Substance Absue Research Centre, Shammah.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">242</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Siddig Ibrahim Abdelwahab&lt;sup&gt;*1&lt;/sup&gt;, Syam Mohan&lt;sup&gt;2&lt;/sup&gt;, Manal Moahmed Elhassan Taha&lt;sup&gt;2&lt;/sup&gt;, Rashad Bin Mohammed Alsanosy&lt;sup&gt;1&lt;/sup&gt; and Hamed Karimian&lt;sup&gt;3 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Substance Abuse Research Centre, Jazan University, 11420, Jazan, Saudi Arabia&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Medical Research Center, Jazan University, 11420, Jazan, Saudi Arabia&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmacy, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Swati Vyas</style></author><author><style face="normal" font="default" size="100%">Sumita Kachhwaha</style></author><author><style face="normal" font="default" size="100%">S. L. Kothari</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative analysis of phenolic contents and total antioxidant capacity of Moringa oleifera Lam</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">oxidation.</style></keyword><keyword><style  face="normal" font="default" size="100%">sequential extract</style></keyword><keyword><style  face="normal" font="default" size="100%">total flavonoid content</style></keyword><keyword><style  face="normal" font="default" size="100%">total phenolic content</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">01/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">44-51</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Accumulation of reactive species higher than permissible limits in biological systems may lead to various degenerative disorders due to oxidative damage. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Oxidation is a serious concern faced by the food industry causing deterioration of shelved-food quality. Antioxidant compounds like polyphenolics scavenge such free radicals and thus protect against oxidative stress. Consumption of polyphenol-rich plants as dietary component confers protection against such cellular damage. &lt;strong&gt;Results:&lt;/strong&gt; Present study explores antioxidant capacity, total phenolic content (TPC) and total flavonoid content (TFC) of different extracts prepared from various parts of &lt;em&gt;Moringa oleifera &lt;/em&gt;Lam. Higher TPC, TFC and antioxidant activity was shown by methanolic extracts followed by aqueous, petroleum benzene and chloroform extracts.The present study suggests that all the extracts might act as radical scavengers to certain extent possibly due to presence of polyphenolic compounds. &lt;strong&gt;Conclusion:&lt;/strong&gt; &lt;em&gt;M. oleifera&lt;/em&gt; exhibits strong antioxidant activity and could serve as prospective source of natural antioxidants to food and health industries.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">44</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Swati Vyas&lt;sup&gt;1&lt;/sup&gt;, Sumita Kachhwaha&lt;sup&gt;1&lt;/sup&gt; and S. L. Kothari&lt;sup&gt;1,2*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Botany, University of Rajasthan, Jaipur, Rajasthan, India&amp;ndash;302004.&lt;/p&gt;

&lt;p&gt;&lt;sup&gt;2&lt;/sup&gt;Institute of Biotechnology, Amity University, Rajasthan, Jaipur, Rajasthan, India-302019.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Deepa Chundayil Kalarickal</style></author><author><style face="normal" font="default" size="100%">Sujith Samraj</style></author><author><style face="normal" font="default" size="100%">Darsana Udayan</style></author><author><style face="normal" font="default" size="100%">Priya Manakkulaparambil Narayanan</style></author><author><style face="normal" font="default" size="100%">Sreedevi Ramachandran</style></author><author><style face="normal" font="default" size="100%">Sreeshitha Sreedharan Gouri</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of various extracts of Ocimum sanctum and Mallotus phillipensis on Setaria digitata</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Albendazole</style></keyword><keyword><style  face="normal" font="default" size="100%">Anthelmintic</style></keyword><keyword><style  face="normal" font="default" size="100%">Mallotus phillipensis</style></keyword><keyword><style  face="normal" font="default" size="100%">Ociumum sanctum</style></keyword><keyword><style  face="normal" font="default" size="100%">Setaria digitata</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Nov-Dec 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">344-347</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;The anthelmintic activity of various extracts of leaves of Ocimum sanctum and Mallotus phillipensis was assessed in vitro against Setaria digitata. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The leaves of Ocimum sanctum and Mallotus phillipensis were collected and were extracted using methanol, dried and stored under refrigeration till further use. The aqueous extract was taken as a decoction. The methanolic extract was further fractionated by taking solvents of increasing polarity viz, hexane, chloroform, n-butanol and water. The extract as well as the fractions were analysed qualitatively for various phytochemical constituents. Fresh nematodes (Setaria digitata) were recovered manually from the peritoneum of infested buffalo, were washed and transferred to the extract containing petriplates (concentrations of 50, 25, 12.5, 6.25, 3.125 and 1.56 mg/ml) immediately and the motility/death of Setaria digitata was noted. &lt;strong&gt;Results:&lt;/strong&gt; The presence of flavonoids and tannins were detected in all the extracts where was phenolics as absent in the hexane fraction. The methanolic extract of Tulsi and Kamla produced death of nematodes in concentrations of 3.125 mg/ml and the extract of tulsi was found to be more potent. Similar results were also observed in the case of hydro alcoholic extract whereas the aqueous extract showed no effect. The chloroform fraction of Ocimum sanctum and n-butanol and chloroform fractions of Mallotus were equally potent in inhibiting the motility and producing death of the worms. The control drug, albendazole produced death in 30 minutes in both the concentrations. &lt;strong&gt;Conclusion:&lt;/strong&gt; It could be concluded that higher doses of the extract are as potent as albendazole.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">344</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Deepa Chundayil Kalarickal, Sujith Samraj*, Darsana Udayan, Priya Manakkulaparambil Narayanan, Sreedevi Ramachandran and Sreeshitha Sreedharan Gouri&lt;/strong&gt; Department of Veterinary Pharmacology and Toxicology, College of Veterinary and Animal Sciences, Pookode Kerala, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ramaraj Thirugnanasampandan</style></author><author><style face="normal" font="default" size="100%">Gunasekar Ramya</style></author><author><style face="normal" font="default" size="100%">Madhusudhanan Gogulramnath</style></author><author><style face="normal" font="default" size="100%">Rajarajeswaran Jayakumar</style></author><author><style face="normal" font="default" size="100%">M.S. Kanthimathi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of cytotoxic, DNA protecting and LPS induced MMP-9 down regulation activities of Plectranthus amboinicus (Lour) Spreng. essential oil</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antigenotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Essential oil</style></keyword><keyword><style  face="normal" font="default" size="100%">RT- PCR.</style></keyword><keyword><style  face="normal" font="default" size="100%">Zymogram</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">01/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">32-36</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;em&gt;Plectranthus amboinicus&lt;/em&gt; (Lour) Spreng is a known medicinal plant used in Siddha and Ayurveda medicines in India. It has enormous medicinal potential to treat various diseases. &lt;strong&gt;Methods:&lt;/strong&gt; The present study focused on the use of essential oil obtained from the leaves of Plectranthusamboinicusto test cytotoxicity against breast (MCF-7) and colorectal (HT-29) cancer cell lines, to protect DNA from H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; induced genotoxicity through comet assay and to treat inflammation in lipopolysaccharide (LPS) induced over expression of matrix metalloproteinase-9 (MMP-9) in human peripheral blood mononuclear cells (PBMCs) by gelatin zymogram and inhibition at transcriptional level confirmed using RT-PCR (reverse transcriptase polymerase chain reaction). &lt;strong&gt;Results:&lt;/strong&gt; Cytotoxicity of essential oil against MCF-7 and HT-29 cancer cell lines revealed the IC&lt;sub&gt;50&lt;/sub&gt; values of 53 &amp;plusmn; 0.01 and 87 &amp;plusmn; 0.01 &amp;mu;g/mL respectively. At 200 &amp;mu;g/mL essential oil protected against 75% of DNA damage in 3T3-L1 fibroblast cells. Essential oil showed significant reduction in production of MMP-9 in a concentration dependent manner. &lt;strong&gt;Conclusion:&lt;/strong&gt; Overall, the results showed that essential oil of &lt;em&gt;P. amboinicus&lt;/em&gt; is a potent bioactive substance and it could be used in herbal medicine preparations.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">32</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ramaraj Thirugnanasampandan&lt;sup&gt;a,*&lt;/sup&gt;, Gunasekar Ramya&lt;sup&gt;a&lt;/sup&gt;, Madhusudhanan Gogulramnath&lt;sup&gt;a&lt;/sup&gt;, Rajarajeswaran Jayakumar&lt;sup&gt;b&lt;/sup&gt;, M.S. Kanthimathi&lt;sup&gt;b&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;a&lt;/sup&gt;Laboratory of Plant Tissue Culture and Molecular Bioprospection, PG and Research Department of Biotechnology, Kongunadu Arts and Science College, GN Mills, Coimbatore, Tamil Nadu, India.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;b&lt;/sup&gt;Department of Molecular Medicine, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ramaraj Thirugnanasampandan</style></author><author><style face="normal" font="default" size="100%">Gunasekar Ramya</style></author><author><style face="normal" font="default" size="100%">Madhusudhanan Gogulramnath</style></author><author><style face="normal" font="default" size="100%">Rajarajeswaran Jayakumar</style></author><author><style face="normal" font="default" size="100%">M.S. Kanthimathi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation of cytotoxic, DNA protecting and LPS induced MMP-9 down regulation activities of Plectranthus amboinicus (Lour) Spreng. essential oil.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antigenotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Essential oil</style></keyword><keyword><style  face="normal" font="default" size="100%">RT- PCR</style></keyword><keyword><style  face="normal" font="default" size="100%">Zymogram</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">27th Nov, 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">32-36</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt;&lt;em&gt;Plectranthus amboinicus&lt;/em&gt; (Lour) Spreng is a known medicinal plant used in Siddha and Ayurveda medicines in India. It has enormous medicinal potential to treat various diseases. &lt;strong&gt;Methods:&lt;/strong&gt; The present study focused on the use of essential oil obtained from the leaves of &lt;em&gt;Plectranthus amboinicus&lt;/em&gt; to test cytotoxicity against breast (MCF-7) and colorectal (HT-29) cancer cell lines, to protect DNA from H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt; induced genotoxicity through comet assay and to treat inflammation in lipopolysaccharide (LPS) induced over expression of matrix metalloproteinase-9 (MMP-9) in human peripheral blood mononuclear cells (PBMCs) by gelatin zymogram and inhibition at transcriptional level confirmed using RT-PCR (reverse transcriptase polymerase chain reaction). &lt;strong&gt;Results:&lt;/strong&gt; Cytotoxicity of essential oil against MCF-7 and HT-29 cancer cell lines revealed the IC50 values of 53 &amp;plusmn; 0.01 and 87 &amp;plusmn; 0.01&amp;mu;g/mL respectively. At 200 &amp;mu;g/mL essential oil protected against 75% of DNA damage in 3T3-L1 fibroblast cells. Essential oil showed significant reduction in production of MMP-9 in a concentration dependent manner. &lt;strong&gt;Conclusion:&lt;/strong&gt; Overall, the results showed that essential oil of &lt;em&gt;P. amboinicus&lt;/em&gt; is a potent bioactive substance and it could be used in herbal medicine preparations.&lt;br /&gt;&lt;strong&gt;Key words:&lt;/strong&gt;&lt;em&gt; Essential oil , Cytotoxicity , Antigenotoxicity, Zymogram, RT- PCR.&lt;/em&gt;&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><custom1><style face="normal" font="default" size="100%">Ramaraj Thirugnanasampandan, Gunasekar Ramya, Madhusudhanan Gogulramnath, Rajarajeswaran Jayakumar, M.S. Kanthimathi</style></custom1><section><style face="normal" font="default" size="100%">32</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ramaraj Thirugnanasampandan&lt;sup&gt;a,*&lt;/sup&gt;, Gunasekar Ramya&lt;sup&gt;a&lt;/sup&gt;, Madhusudhanan Gogulramnath&lt;sup&gt;a&lt;/sup&gt;, Rajarajeswaran Jayakumar&lt;sup&gt;b&lt;/sup&gt;, M.S. Kanthimathi&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;b&lt;/strong&gt;&lt;/sup&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;a&lt;/sup&gt;Laboratory of Plant Tissue Culture and Molecular Bioprospection, PG and Research Department of Biotechnology, Kongunadu Arts and Science College, GN Mills, Coimbatore, Tamil Nadu, India&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;b&lt;/sup&gt;Department of Molecular Medicine, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Haroon Khan</style></author><author><style face="normal" font="default" size="100%">Murad Ali Khan</style></author><author><style face="normal" font="default" size="100%">Abdul Rauf</style></author><author><style face="normal" font="default" size="100%">Ashhad Haleemi</style></author><author><style face="normal" font="default" size="100%">Shivkanya Fuloria</style></author><author><style face="normal" font="default" size="100%">Neeraj Kumar Fuloria</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Inhibition on Urease and Thermal Induced Protein Denaturation of commonly used Antiulcer Herbal Products. Study based on in-vitro assays</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Akseer ULCER</style></keyword><keyword><style  face="normal" font="default" size="100%">Antiurease activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Endemali</style></keyword><keyword><style  face="normal" font="default" size="100%">Thermal induced protein denaturation.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">16th Jan, 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">147-151</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;In-vitro&lt;/em&gt; urease inhibitory and thermal induced protein denaturation inhibitory activitieswasperformed for two commonly used herbal productsEndemali and Akseer ULCER in the treatment of ulcers.&lt;strong&gt;Objectives: &lt;/strong&gt;to evaluate the antiulcer potential of two commonly used herbal products, Endemali, Akseer ULCER. &lt;strong&gt;Material and Method:&lt;/strong&gt; In urease inhibitory assay , enzyme solution, extract, diferentregaents added and absorbance was measured at 630 nm (50 min, pH 8.2) and thiourea used as standard. In protein denaturation assay the egg albumin was mixed with different concentration of test compounds, buffer absorbance was measured. Aspirin was used as standard. &lt;strong&gt;Results:&lt;/strong&gt; The Endemalihad a profound effect on the urease activity in a concentration dependent manner with EC&lt;sub&gt;50&lt;/sub&gt; valueof 0.468 mg/ml. The Akseer ULCER antagonized the urease activity markedly with EC&lt;sub&gt;50 &lt;/sub&gt;value of 0.374 mg/ml.These tested herbal products caused marked inhibition of thermal induced protein denaturation in a concentration dependent manner. The potency in the form of EC&lt;sub&gt;50 &lt;/sub&gt;for Endemali, Akseer ULCER was measured as 323, 337 &amp;micro;g/mlrespectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; In short, the tested herbal drug showed strong inhibition on urease activity and inhibition on thermal induced protein denaturation thus our study validated their uses in the treatment of ulcers.&lt;/p&gt;&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Akseer ULCER, Endemali, Antiurease activity, Thermal induced protein denaturation.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">147</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Haroon Khan&lt;sup&gt;*1&lt;/sup&gt;, Murad Ali Khan&lt;sup&gt;2&lt;/sup&gt;, Abdul Rauf&lt;sup&gt;3&lt;/sup&gt;, Ashhad Haleemi&lt;sup&gt;4&lt;/sup&gt;, Shivkanya Fuloria&lt;sup&gt;5&lt;/sup&gt;, Neeraj Kumar Fuloria&lt;sup&gt;5 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacy, Abdul Wali Khan University Mardan 23200, Pakistan&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemistry, Kohat University of Science and Technology, Kohat, Pakistan&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Institute of Chemical Sciences, University of Peshawar, Peshawar -25120, Pakistan&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacy, University of Peshawar, Peshawar -25120, Pakistan&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Pharmcy, AIMST University,Semeling Campus, Bedong, Kedah Darul Aman-08100, Malyasia&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Haroon Khan</style></author><author><style face="normal" font="default" size="100%">Murad Ali Khan</style></author><author><style face="normal" font="default" size="100%">Abdul Rauf</style></author><author><style face="normal" font="default" size="100%">Ashhad Haleemi</style></author><author><style face="normal" font="default" size="100%">Shivkanya Fuloria</style></author><author><style face="normal" font="default" size="100%">Neeraj Kumar Fuloria</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Inhibition on Urease and Thermal Induced Protein Denaturation of commonly used Antiulcer Herbal Products. Study based on in-vitro assays</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Akseer ULCER</style></keyword><keyword><style  face="normal" font="default" size="100%">Antiurease activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Endemali</style></keyword><keyword><style  face="normal" font="default" size="100%">in-vitro assay</style></keyword><keyword><style  face="normal" font="default" size="100%">Thermal induced protein denaturation.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">01/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">147-151</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;In-vitro&lt;/em&gt; urease inhibitory and thermal induced protein denaturation inhibitory activities was performed for two commonly used herbal products Endemali and Akseer ULCER in the treatment of ulcers. &lt;strong&gt;Objectives:&lt;/strong&gt; To evaluate the antiulcer potential of two commonly used herbal products, Endemali, Akseer ULCER. &lt;strong&gt;Material and Method:&lt;/strong&gt; In urease inhibitory assay, enzyme solution, extract, diferent regaents added and absorbance was measured at 630 nm (50 min, pH 8.2) and thiourea used as standard. In protein denaturation assay, the egg albumin was mixed with different concentration of test compounds, buffer absorbance was measured. Aspirin was used as standard. &lt;strong&gt;Results:&lt;/strong&gt; The Endemali had a profound effect on the urease activity in a concentration dependent manner with EC50value of 0.468 mg/ml. The Akseer ULCER antagonized the urease activity markedly with EC&lt;sub&gt;50&lt;/sub&gt; value of 0.374 mg/ml. These tested herbal products caused marked inhibition of thermal induced protein denaturation in a concentration dependent manner. The potency in the form of EC&lt;sub&gt;50&lt;/sub&gt; for Endemali, Akseer ULCER was measured as 323, 337 &amp;mu;g/ml respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; In short, the tested herbal drug showed strong inhibition on urease activity and inhibition on thermal induced protein denaturation thus our study validated their uses in the treatment of ulcers.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">147</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Haroon Khan&lt;sup&gt;*1&lt;/sup&gt;, Murad Ali Khan&lt;sup&gt;2&lt;/sup&gt;, Abdul Rauf&lt;sup&gt;3&lt;/sup&gt;, Ashhad Haleemi&lt;sup&gt;4&lt;/sup&gt;, Shivkanya Fuloria&lt;sup&gt;5&lt;/sup&gt;, Neeraj Kumar Fuloria&lt;sup&gt;5&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacy, Abdul Wali Khan University Mardan 23200, Pakistan.&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Chemistry, Kohat University of Science and Technology, Kohat, Pakistan.&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Institute of Chemical Sciences, University of Peshawar, Peshawar-25120, Pakistan.&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Department of Pharmacy, University of Peshawar, Peshawar-25120, Pakistan.&lt;/p&gt;

&lt;p style=&quot;text-align:justify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Pharmcy, AIMST University,Semeling Campus, Bedong, Kedah Darul Aman-08100, Malyasia.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sowmyashree Gangaraju</style></author><author><style face="normal" font="default" size="100%">Bhagyalakshmi Manjappa</style></author><author><style face="normal" font="default" size="100%">Girish Kesturu Subbaiah</style></author><author><style face="normal" font="default" size="100%">Kemparaju Kempaiah</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Jackfruit (Artocarpus heterophyllus) seed extract exhibits fibrino(geno)lytic activity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Fibrino(geno)lysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Hemostasis</style></keyword><keyword><style  face="normal" font="default" size="100%">Jackfruit</style></keyword><keyword><style  face="normal" font="default" size="100%">Moraceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Non-hemorrhagic</style></keyword><keyword><style  face="normal" font="default" size="100%">Serine/cysteine protease.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">09th Mar, 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">171-177</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; The current study assesses the fibrinogen and fibrin clot hydrolyzing activities of aqueous seed extract of Jackfruit (AqSEJ).&lt;strong&gt; Methods:&lt;/strong&gt; The protein banding pattern of AqSEJ (100 &amp;mu;g) was analyzed on SDS-PAGE. The proteolytic activity of AqSEJ was confirmed by spectrophotometer and zymography experiments. Fibrinogen, fibrin and plasma protein hydrolyzing activities of AqSEJ were analyzed on SDS-PAGE under reduced conditions. Plasminogen activation and indirect hemolytic activities was analyzed using spectrophotometer. The non-toxic property of AqSEJ was tested by edema, hemorrhage in experimental mice. &lt;strong&gt;Results: &lt;/strong&gt;AqSEJ exhibited proteolytic activity and the specific activity was found to be 1.04 units/mg/min. Furthermore, AqSEJ non-specifically hydrolyzed A&amp;alpha;, followed by B&amp;beta; and &amp;gamma; chains of human fibrinogen and specifically hydrolyzed &amp;alpha; polymer and &amp;alpha; chain of partially cross linked human fibrin clot without affecting &amp;beta; chain and &amp;gamma;-&amp;gamma; dimer even up to the tested dose of 30 &amp;micro;g for the incubation period of 8 hours. Importantly, AqSEJ did not hydrolyze other plasma proteins and devoid of plasminogen activation property. The proteolytic activity of AqSEJ was completely neutralized by PMSF and IAA, while EDTA, EGTA, 1,10-Phenanthroline did not, suggesting the presence of serine and cysteine family proteases. Moreover, AqSEJ did not cause edema and hemorrhage in experimental mice up to the tested dose of 200 &amp;micro;g and nontoxic to RBC cells. &lt;strong&gt;Conclusion: &lt;/strong&gt;AqSEJ hydrolyzes fibrinogen and fibrin clot and non-toxic in nature. Hence, this work showcases the potential applications of Jack fruit seed proteases in the treatment of thrombotic disorders.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Fibrino(geno)lysis, Hemostasis, Jackfruit, Moraceae, Non-hemorrhagic, Serine/cysteine protease.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">171</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Sowmyashree Gangaraju&lt;sup&gt;1&lt;/sup&gt;, Bhagyalakshmi Manjappa&lt;sup&gt;1&lt;/sup&gt;, Girish Kesturu Subbaiah&lt;sup&gt;1&lt;/sup&gt;, Kemparaju Kempaiah&lt;sup&gt;2&lt;/sup&gt;, Rangaiah Shashidhara Murthy&lt;sup&gt;3&lt;/sup&gt;, Jane Hoover Plow&lt;sup&gt;4&lt;/sup&gt;, Sebastin Santhosh Martin&lt;sup&gt;5&lt;/sup&gt;, Manohar Shinde&lt;sup&gt;1&lt;/sup&gt;, and Devaraja Sannaningaiah&lt;sup&gt;1*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1,*&lt;/sup&gt;Department of Studies and Research in Biochemistry and Centre for Bioscience and Innovation, Tumkur University, Tumkur- 572103, India&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Departments of Studies in Biochemistry, University of Mysore, Manasagangothry, Mysore-570 006, India&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmaceutical Sciences, Philadelphia College of Osteopathic Medicine. Atlanta, Georgia, USA&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Joseph J. Jacobs Center for Thrombosis and Vascular Biology, Department of Molecular Cardiology, Cleveland Clinic Lerner Research Institute, Cleveland, OH&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Department of Medical Biochemistry and Biophysics, Karolinska Institute, SE 17177, Stockhlm, Sweden&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sowmyashree Gangaraju</style></author><author><style face="normal" font="default" size="100%">Bhagyalakshmi Manjappa</style></author><author><style face="normal" font="default" size="100%">Girish Kesturu Subbaiah</style></author><author><style face="normal" font="default" size="100%">Kemparaju Kempaiah</style></author><author><style face="normal" font="default" size="100%">Rangaiah Shashidharamurthy</style></author><author><style face="normal" font="default" size="100%">Jane Hoover Plow</style></author><author><style face="normal" font="default" size="100%">Sebastin Santhosh Martin</style></author><author><style face="normal" font="default" size="100%">Manohar Shinde</style></author><author><style face="normal" font="default" size="100%">Devaraja Sannaningaiah</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Jackfruit (Artocarpus heterophyllus) seed extract exhibits fibrino(geno)lytic activity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Fibrino(geno)lysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Hemostasis</style></keyword><keyword><style  face="normal" font="default" size="100%">Jackfruit</style></keyword><keyword><style  face="normal" font="default" size="100%">Moraceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Non-hemorrhagic</style></keyword><keyword><style  face="normal" font="default" size="100%">Serine/cysteine protease.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">01/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">171-177</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Objective: &lt;/strong&gt;The current study assesses the fibrinogen and fibrin clot hydrolyzing activities of aqueous seed extract of Jackfruit (AqSEJ). &lt;strong&gt;Methods:&lt;/strong&gt; The protein banding pattern of AqSEJ (100 &amp;mu;g) was analyzed on SDS-PAGE. The proteolytic activity of AqSEJ was confirmed by spectrophotometer and zymography experiments. Fibrinogen, fibrin and plasma protein hydrolyzing activities of AqSEJ were analyzed on SDS-PAGE under reduced conditions. Plasminogen activation and indirect hemolytic activities was analyzed using spectrophotometer. The non-toxic property of AqSEJ was tested by edema, hemorrhage in experimental mice. &lt;strong&gt;Results:&lt;/strong&gt; AqSEJ exhibited proteolytic activity and the specific activity was found to be 1.04 units/mg/min. Furthermore, AqSEJ non-specifically hydrolyzed A&amp;alpha;, followed by B&amp;beta; and &amp;gamma; chains of human fibrinogen and specifically hydrolyzed &amp;alpha; polymer and &amp;alpha; chain of partially cross linked human fibrin clot without affecting &amp;beta; chain and &amp;gamma;-&amp;gamma; dimer even up to the tested dose of 30 &amp;micro;g for the incubation period of 8 hours. Importantly, AqSEJ did not hydrolyze other plasma proteins and devoid of plasminogen activation property. The proteolytic activity of AqSEJ was completely neutralized by PMSF and IAA, while EDTA, EGTA, 1,10-Phenanthroline did not, suggesting the presence of serine and cysteine family proteases. Moreover, AqSEJ did not cause edema and hemorrhage in experimental mice up to the tested dose of 200 &amp;micro;g and non-toxic to RBC cells. &lt;strong&gt;Conclusion:&lt;/strong&gt; AqSEJ hydrolyzes fibrinogen and fibrin clot and non-toxic in nature. Hence, this work showcases the potential applications of Jack fruit seed proteases in the treatment of thrombotic disorders.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">171</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Sowmyashree Gangaraju&lt;sup&gt;1&lt;/sup&gt;, Bhagyalakshmi Manjappa&lt;sup&gt;1&lt;/sup&gt;, Girish Kesturu Subbaiah&lt;sup&gt;1&lt;/sup&gt;, Kemparaju Kempaiah&lt;sup&gt;2&lt;/sup&gt;, Rangaiah Shashidharamurthy&lt;sup&gt;3&lt;/sup&gt;, Jane Hoover Plow&lt;sup&gt;4&lt;/sup&gt;, Sebastin Santhosh Martin&lt;sup&gt;5&lt;/sup&gt;, Manohar Shinde&lt;sup&gt;1&lt;/sup&gt;, and Devaraja Sannaningaiah&lt;sup&gt;1*&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1,*&lt;/sup&gt;Department of Studies and Research in Biochemistry and Centre for Bioscience and Innovation, Tumkur University, Tumkur- 572103, India.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Studies in Biochemistry, University of Mysore, Manasagangothry, Mysore-570 006, India.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Pharmaceutical Sciences, Philadelphia College of Osteopathic Medicine. Atlanta, Georgia, USA .&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Joseph J. Jacobs Center for Thrombosis and Vascular Biology, Department of Molecular Cardiology, Cleveland Clinic Lerner Research Institute, Cleveland, OH 5Department of Medical Biochemistry and Biophysics, Karolinska Institute, SE 17177, Stockhlm, Sweden.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shweta Kumar</style></author><author><style face="normal" font="default" size="100%">Balakrishnan Natarajan</style></author><author><style face="normal" font="default" size="100%">Lakshmi Puthanparambil Kanakamma</style></author><author><style face="normal" font="default" size="100%">Toppo Fedelic Ashish</style></author><author><style face="normal" font="default" size="100%">Rajesh Singh Pawar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostical and Phytochemical evaluation of Ventilago calyculata Tul. (Bark)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">standardization</style></keyword><keyword><style  face="normal" font="default" size="100%">total flavonoid content</style></keyword><keyword><style  face="normal" font="default" size="100%">total phenolic content</style></keyword><keyword><style  face="normal" font="default" size="100%">Ventilago denticulata Willd</style></keyword><keyword><style  face="normal" font="default" size="100%">Ventilago madraspatana var. calyculata (Tul.) King.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">01/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">271-275</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; &lt;em&gt;Ventilago calyculata&lt;/em&gt; Tul. (&amp;lsquo;kevati&amp;rsquo;), is found throughout India as climbing shrub. It is widely used in various traditional system of medicine. &lt;strong&gt;Objective:&lt;/strong&gt; In the present work pharmacognostical standardization has been developed for the systematic identification of the bark of &lt;em&gt;Ventilago calyculata&lt;/em&gt;. Phenols and flavonoids were also quantified. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Morphological, microscopical and phytochemical studies were performed. Various physicochemical parameters conforming the identity, quality, purity of the bark. The quantity of phenols and flavonoids were estimated. &lt;strong&gt;Results:&lt;/strong&gt; The bark was oval, brownish yellow, bitter with characteristic odour and rough texture. The microscopical studies revealed the presence of cork with brownish contents, crimson inner cork, collenchyma, cellulosic parenchyma with cuboidal calcium oxalate crystals and schlereids. The total ash value, acid insoluble ash value and water soluble ash values of stem bark were found to be 15% w/w, 3.4% w/w and 11.6% w/w respectively. The percentage yields, total phenolic content and the total flavonoid content of the petroleum ether, chloroform, ethyl acetate, ethanol and aqueous extracts were 2.77% w/w, 2.66% w/w, 3.8% w/w, 5.8% w/w, 11.0% w/w; 2.16 &amp;plusmn; 0.04, 4.16 &amp;plusmn; 1.04, 9.12 &amp;plusmn; 1.14, 7.16&amp;plusmn;1.16, 1.16 &amp;plusmn;1.02 mg/g (gallic acid equivalent) and 4.5 &amp;plusmn; 0.55, 8.20 &amp;plusmn; 1.12, 10.1 &amp;plusmn; 0. 26, 6.5 &amp;plusmn; 1.3, 0.66 &amp;plusmn; 1.13 mg/g (rutin equivalent) respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; There was a need to evaluate the extracts of the plant in order to provide scientific proof for its application and to explore the possibility of treating various diseases and disorders. Literature review indicates that very less work has been done on this plant and there is a wide scope for investigation.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">271</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Shweta Kumar&lt;sup&gt;2&lt;/sup&gt;, Balakrishnan Natarajan&lt;sup&gt;1&lt;/sup&gt;, Lakshmi Puthanparambil Kanakamma&lt;sup&gt;2&lt;/sup&gt;, Toppo Fedelic Ashish&lt;sup&gt;2&lt;/sup&gt; and Rajesh Singh Pawar&lt;sup&gt;2*&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Technocrats Institute of Technology-Pharmacy, Bhopal, Madhya Pradesh, 462021, INDIA.&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacognosy and Phytochemistry Laboratory, Faculty of Pharmacy, VNS Group of Institutions, Neelbud, Bhopal, Madhya Pradesh, 462044, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kumar Shweta</style></author><author><style face="normal" font="default" size="100%">Balakrishnan N</style></author><author><style face="normal" font="default" size="100%">Lakshmi P. K</style></author><author><style face="normal" font="default" size="100%">Toppo F. A</style></author><author><style face="normal" font="default" size="100%">Toppo F. A</style></author><author><style face="normal" font="default" size="100%">Pawar RS</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostical and phytochemical evaluation of Ventilago calyculata Tul. (Bark)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">standardization</style></keyword><keyword><style  face="normal" font="default" size="100%">total flavonoid content</style></keyword><keyword><style  face="normal" font="default" size="100%">total phenolic content</style></keyword><keyword><style  face="normal" font="default" size="100%">Ventilago denticulata Willd</style></keyword><keyword><style  face="normal" font="default" size="100%">Ventilago madraspatana var. calyculata (Tul.) King.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">29th Apr, 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">1-1</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt;&lt;em&gt;Ventilago calyculata&lt;/em&gt; Tul. (&amp;lsquo;kevati&amp;rsquo;), is found throughout India as climbing shrub. It is widely used in various traditional system of medicine.&lt;strong&gt; Objective: &lt;/strong&gt;In the present work pharmacognostical standardization has been developed for the systematic identification of the bark of Ventilago calyculata. Phenols and flavonoids were also quantified. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Morphological, microscopical and phytochemical studies were performed. Various physicochemical parameters conforming the identity, quality, purity of the bark. The quantity of phenols and flavonoids were estimated. &lt;strong&gt;Results:&lt;/strong&gt; The bark was oval, brownish yellow, bitter with characteristic odour and rough texture. The microscopical studies revealed the presence of cork with brownish contents, crimson inner cork, collenchyma, cellulosic parenchyma with cuboidal calcium oxalate crystals and schlereids. The total ash value, acid insoluble ash value and water soluble ash values of stem bark were found to be 15% w/w, 3.4% w/w and 11.6% w/w respectively. The percentage yields, total phenolic content and the total flavonoid content of the petroleum ether, chloroform, ethyl acetate, ethanol and aqueous extracts were 2.77% w/w, 2.66% w/w, 3.8% w/w, 5.8% w/w, 11.0% w/w; 2.16 &amp;plusmn; 0.04, 4.16 &amp;plusmn; 1.04, 9.12 &amp;plusmn; 1.14, 7.16&amp;plusmn;1.16, 1.16&amp;plusmn;1.02 mg/g (gallic acid equivalent) and 4.5 &amp;plusmn; 0.55, 8.20 &amp;plusmn; 1.12, 10.1 &amp;plusmn; 0. 26, 6.5 &amp;plusmn; 1.3, 0.66 &amp;plusmn; 1.13 mg/g (rutin equivalent) respectively. &lt;strong&gt;Conclusion: &lt;/strong&gt;There was a need to evaluate the extracts of the plant in order to provide scientific proof for its application and to explore the possibility of treating various diseases and disorders. Literature review indicates that very less work has been done on this plant and there is a wide scope for investigation.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key Words:&lt;/strong&gt; Standardization, Total flavonoid content, Total phenolic content, Ventilago denticulata Willd, Ventilago madraspatana var. calyculata (Tul.) King.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Kumar Shweta&lt;sup&gt;2&lt;/sup&gt;, Balakrishnan N&lt;sup&gt;1&lt;/sup&gt;, Lakshmi P. K&lt;sup&gt;2&lt;/sup&gt;, Toppo F. A&lt;sup&gt;2&lt;/sup&gt; and Pawar R. S&lt;sup&gt;2* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy, Technocrats Institute of Technology-Pharmacy, Bhopal, Madhya Pradesh, 462021, INDIA.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Pharmacognosy and Phytochemistry Laboratory, Faculty of Pharmacy, VNS Group of Institutions, Neelbud, Bhopal, Madhya Pradesh,462044, INDIA.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Manisha Khaneja</style></author><author><style face="normal" font="default" size="100%">Sumeet Gupta</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Anupam Sharma</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostical and Preliminary Phytochemical Investigations on fruit of Vaccinium macrocarpon aiton</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Fruit</style></keyword><keyword><style  face="normal" font="default" size="100%">microscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">Morphoanataomical</style></keyword><keyword><style  face="normal" font="default" size="100%">Physicochemical analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Vaccinium macrocarpon aiton</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Nov-Dec 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">333-338</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Vaccinium species are hostile nutraceutical fruit in India as well as all over the world. In recent years, Vaccinium macrocarpon Aiton is used as a functional food for treating various diseases without authentication. &lt;strong&gt;Objective:&lt;/strong&gt; The current work was investigated to perform the morphoanatomical and physicochemical of Vaccinium macrocarpon Aiton fruit. &lt;strong&gt;Method: &lt;/strong&gt;Pharmacognostic studies were carried out for different parameters include organoleptic, macroscopic, microscopic, fluorescence and physicochemical analysis.&lt;strong&gt; Results:&lt;/strong&gt; The fruit was shining burgundy purple in colour having smooth lustrous surface, globular to ellipsoidal in shape with 10-15 mm in length and diameter was 9 mm. The main microscopic characteristic of fruit showed ovules, compact angular parenchyma cells, developed sclerenchymatous outer sheath, central xylem and phloem strands. Fruit powder showed oil bodies, spherical parenchyma cells in large thick masses and walls of the epicarp demonstrated cellulose content. Further, physicochemical examination of fruit powder showed loss on drying, total ash, insoluble ash as 9.23, 7.8, and 9.16% w/w respectively. The water and alcohol soluble extractives values of the fruit were 24.74 and 76.88% respectively. Anthocyanins and flavonids were also confirmed by phytochemical screening.&lt;strong&gt; Conclusion:&lt;/strong&gt; A variety of pharmacognostic features was found in fruitful way which may help in identification and standardization of Vaccinium macrocarpon Aiton fruit in a crude form.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">333</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Manisha Khaneja&lt;sup&gt;1&lt;/sup&gt;, Sumeet Gupta&lt;sup&gt;*1&lt;/sup&gt; and Anupam Sharma&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt; &lt;sup&gt;1&lt;/sup&gt;Department of Pharmacology, M. M. College of Pharmacy, M. M. University, Mullana, (Ambala), Haryana, India. &lt;sup&gt;2&lt;/sup&gt;University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">G Phani Kumar</style></author><author><style face="normal" font="default" size="100%">K.R. Anilakumar</style></author><author><style face="normal" font="default" size="100%">S. Naveen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemicals Having Neuroprotective Properties from Dietary Sources and Medicinal Herbs</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Dietary sources.</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal herbs</style></keyword><keyword><style  face="normal" font="default" size="100%">Neuroprotection</style></keyword><keyword><style  face="normal" font="default" size="100%">Nootropics</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">27th Nov, 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">01-17</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;Many neuropsychiatric and neurodegenerative disorders, such as Alzheimer&amp;#39;s disease, anxiety, cerebrovascular impairment, depression, seizures, Parkinson&amp;#39;s disease, etc. are predominantly appearing in the current era due to the stress full lifestyle. Treatment of these disorders with prolonged administration of synthetic drugs will lead to severe side effects. In the recent years, scientists have focused the attention of research towards phytochemicals to cure neurological disorders. Nootropic herb refers to the medicinal role of various plants/parts for their neuroprotective properties by the active phytochemicals including alkaloids, steroids, terpenoids, saponins, phenolics, flavonoids, etc. Phytocompounds from medicinal plants play a major part in maintaining the brain&amp;#39;s chemical balance by acting upon the function of receptors for the major inhibitory neurotransmitters. Medicinal plants viz. &lt;em&gt;Valeriana officinalis, Nardostachys jatamansi, Withania somnifera, Bacopa monniera, Ginkgo biloba and Panax ginseng&lt;/em&gt; have been used widely in a variety of traditional systems of therapy because of their adaptogenic, psychotropic and neuroprotective properties. This review highlights the importance of phytochemicals on neuroprotective function and other related disorders, in particular their mechanism of action and therapeutic potential.&lt;/p&gt;&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Neuroprotection, Phytochemicals, Medicinal herbs, Nootropics, Dietary sources.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Review Articles</style></work-type><custom1><style face="normal" font="default" size="100%">G. Phani Kumar, K.R. Anilakumar and S. Naveen</style></custom1><section><style face="normal" font="default" size="100%">1</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;G. Phani Kumar&lt;sup&gt;*&lt;/sup&gt;, K.R. Anilakumar and S. Naveen &lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;Applied Nutrition Division, Defence Food Research Laboratory (DRDO), Ministry of Defence, India&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">G Phani Kumar</style></author><author><style face="normal" font="default" size="100%">K R Anila kumar</style></author><author><style face="normal" font="default" size="100%">S Naveen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemicals Having Neuroprotective Properties from Dietary Sources and Medicinal Herbs</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Dietary sources.</style></keyword><keyword><style  face="normal" font="default" size="100%">Medicinal herbs</style></keyword><keyword><style  face="normal" font="default" size="100%">Neuroprotection</style></keyword><keyword><style  face="normal" font="default" size="100%">Nootropics</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemicals</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">01/2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">1-17</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;Many neuropsychiatric and neurodegenerative disorders, such as Alzheimer&amp;#39;s disease, anxiety, cerebrovascular
impairment, depression, seizures, Parkinson&amp;#39;s disease, etc. are predominantly appearing in the current era due to the stress full lifestyle. Treatment of these disorders with prolonged administration of synthetic drugs will lead to severe side effects. In the recent years, scientists have focused the attention of research towards phytochemicals to cure neurological disorders. Nootropic herb refers to the medicinal role of various plants/parts for their neuroprotective properties by the active phytochemicals including alkaloids, steroids, terpenoids, saponins, phenolics, flavonoids, etc. Phytocompounds from medicinal plants play a major part in maintaining the brain&amp;#39;s chemical balance by acting upon the function of receptors for the major inhibitory neurotransmitters. Medicinal plants viz. &lt;em&gt;Valeriana officinalis&lt;/em&gt;, &lt;em&gt;Nardostachys jatamansi&lt;/em&gt;, &lt;em&gt;Withania somnifera&lt;/em&gt;, &lt;em&gt;Bacopa monniera, Ginkgo biloba and Panax ginseng&lt;/em&gt; have been used widely in a variety of traditional systems of therapy because of their adaptogenic, psychotropic and neuroprotective properties. This review highlights the importance of phytochemicals on neuroprotective function and other related disorders, in particular their mechanism of action and therapeutic potential.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Review Article</style></work-type><section><style face="normal" font="default" size="100%">1</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;G. Phani Kumar*, K.R. Anila kumar and S. Naveen&lt;/strong&gt;&lt;br /&gt;
Applied Nutrition Division, Defence Food Research Laboratory (DRDO), Ministry of Defence, India&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Alpana Kulkarni</style></author><author><style face="normal" font="default" size="100%">Shreya Rumalla</style></author><author><style face="normal" font="default" size="100%">Swati Andhale</style></author><author><style face="normal" font="default" size="100%">Bhanudas Kuchekar</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Ajit Kolatkar</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Taste Masking of Ayurvedic Nutraceutical Formulation by Pan Coating Process</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ayurveda</style></keyword><keyword><style  face="normal" font="default" size="100%">Coating</style></keyword><keyword><style  face="normal" font="default" size="100%">Eudragit E 100</style></keyword><keyword><style  face="normal" font="default" size="100%">Nutraceutical</style></keyword><keyword><style  face="normal" font="default" size="100%">Taste Masking</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jul-Aug 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">215-220</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Background:&lt;/strong&gt; Ayurvedic medicines and nutraceuticals are gaining popularity among physicians and patients for better therapeutic value. Lack of quality standards and problems, in preparing or testing them, are the main hurdles experienced by both the practitioners and the patients.&lt;strong&gt; Objective:&lt;/strong&gt; The objective of the study was to improve the palatability of the Ayurvedic Nutraceutical Preparation (ADS) by masking its bitter taste and to standardize the taste masking procedure. In the present study Eudragit E 100 was used as an acid soluble coating material. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; ADS powder was converted into granules with PVP K30 as a granulating agent and the ADS granules were coated with Eudragit E 100 coating solution by pan coating process. Various IPQC tests namely flow properties, moisture content were performed on the granules before and after coating for determination of endpoint of granulation and coating respectively. The ADS powder and granules were evaluated for bitter taste. &lt;strong&gt;Results:&lt;/strong&gt; ADS granules were advantageous over ADS powder since the flow properties of ADS granules were better than the flow properties of ADS powder, a prerequisite of pan coating process. Eudragit E 100 inhibited the contact in between the plant extracts and the taste buds due to insolubility of Eudragit E 100 in saliva. Sensory evaluation of taste indicated that the taste of coated granules was significantly masked.&lt;strong&gt; Conclusion: &lt;/strong&gt;The bitter taste of ADS was improved successfully with Eudragit E 100 as a coating agent and the pan coating process. An attempt was made to standardize the pan coating process.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">215</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Alpana Kulkarni&lt;sup&gt;*1&lt;/sup&gt;, Shreya Rumalla&lt;sup&gt;1&lt;/sup&gt;, Swati Andhale&lt;sup&gt;1&lt;/sup&gt;, Ajit Kolatkar&lt;sup&gt;2&lt;/sup&gt; and Bhanudas Kuchekar&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt; 1Department of Quality Assurance, MAEER&amp;rsquo;S Maharashtra Institute of Pharmacy, S. No. 124, MIT Campus, Paud Road, Kothrud, Pune-411038, Maharashtra, India 2Department of Integrative Science, Ayurved Consultant, Partner &amp;amp; Director, Arya Rasyan Bioresearch Labs LLP, Pune, Maharashtra, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">AlpanaKulkarni</style></author><author><style face="normal" font="default" size="100%">Shreya Rumalla</style></author><author><style face="normal" font="default" size="100%">Swati Andhale</style></author><author><style face="normal" font="default" size="100%">Ajit Kolatkar</style></author><author><style face="normal" font="default" size="100%">Bhanudas Kuchekar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Taste Masking of AyurvedicNutraceutical Formulation by Pan Coating Process</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ayurveda</style></keyword><keyword><style  face="normal" font="default" size="100%">Coating</style></keyword><keyword><style  face="normal" font="default" size="100%">Eudragit E 100</style></keyword><keyword><style  face="normal" font="default" size="100%">Nutraceutical</style></keyword><keyword><style  face="normal" font="default" size="100%">Taste Masking.</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">29th Apr, 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">215-220</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Ayurvedic medicines and nutraceuticals are gaining popularity among physicians and patients for better therapeutic value. Lack of quality standards and problems, in preparing or testing them, are the main hurdles experienced by both the practitioners and the patients. &lt;strong&gt;Objective: &lt;/strong&gt;The objective of the study was to improve the palatability of the Ayurvedic Nutraceutical Preparation (ADS) by masking its bitter taste and to standardize the taste masking procedure. In the present study Eudragit E 100 was used as an acid soluble coating material. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; ADS powder was converted into granules with PVP K30 as a granulating agent and the ADS granules were coated with Eudragit E 100 coating solution by pan coating process. Various IPQC tests namely flow properties, moisture content were performed on the granules before and after coating for determination of endpoint of granulation and coating respectively. The ADS powder and granules were evaluated for bitter taste. &lt;strong&gt;Results: &lt;/strong&gt;ADS granules were advantageous over ADS powder since the flow properties of ADS granules were better than the flow properties of ADS powder, a prerequisite of pan coating process. Eudragit E 100 inhibited the contact in between the plant extracts and the taste buds due to insolubility of Eudragit E 100 in saliva. Sensory evaluation of taste indicated that the taste of coated granules was significantly masked. &lt;strong&gt;Conclusion: &lt;/strong&gt;The bitter taste of ADS was improved successfully with Eudragit E 100 as a coating agent and the pan coating process. An attempt was made to standardize the pan coating process.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words: &lt;/strong&gt;Ayurveda, Coating, Eudragit E 100, Nutraceutical, Taste Masking.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">215</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Alpana Kulkarni&lt;sup&gt;*1&lt;/sup&gt;, Shreya Rumalla&lt;sup&gt;1&lt;/sup&gt;, Swati Andhale&lt;sup&gt;1&lt;/sup&gt;, Ajit Kolatkar&lt;sup&gt;2&lt;/sup&gt; and Bhanudas Kuchekar&lt;sup&gt;1 &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Quality Assurance, MAEER&amp;rsquo;S Maharashtra Institute of Pharmacy, S. No. 124, MIT Campus, Paud Road, Kothrud, Pune-411038, Maharashtra, India&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Integrative Science, Ayurved Consultant, Partner &amp;amp; Director, Arya Rasyan Bioresearch Labs LLP, Pune, Maharashtra, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Praveen kumar P,</style></author><author><style face="normal" font="default" size="100%">Ramesh A,</style></author><author><style face="normal" font="default" size="100%">Prasad K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Assessment of anti hyperglycemic fractions isolated from Albizia procera stem bark chloroform extract using STZ induced diabetic albino rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Albizia procera</style></keyword><keyword><style  face="normal" font="default" size="100%">hyperglycemia</style></keyword><keyword><style  face="normal" font="default" size="100%">Streptozocin (STZ)</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">8th April 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">29-35</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; The present Study was to identify more effective hypoglycemic fractions from chloroform extract of &lt;em&gt;Albizia procera stem bark&lt;/em&gt;. &lt;strong&gt;Material and methods:&lt;/strong&gt; Isolated fractions of Albizia procera stem bark chloroform extract were given individually to different batches of rats both normal (80 mg/kg of b.wt animals) and STZ induced diabetic rats (160mg/kg b.wt animals) after an overnight fast. The blood glucose levels were measured at 0, 1, 2, 3, 5 and 6 hours after the treatment. Fractions were also treated to STZ induced diabetic rats by chronically (80mg/kg b.wt).&lt;strong&gt; Results:&lt;/strong&gt; The fractions E of &lt;em&gt;Albizia procera stem bark chloroform extract&lt;/em&gt; was shown maximum blood glucose lowering effect in both normal and STZ diabetic rats with acute and chronic treatment. The other fractions are also showing hypoglycemic and antihyperglycemic activity, but the effect is significantly less than that of fraction E. The antihyperglycemic activity of fractions of &lt;em&gt;Albizia procera stem bark chloroform extract&lt;/em&gt; was compared with the treatment of glibenclamide. &lt;strong&gt;Conclusion:&lt;/strong&gt; The present data confirm the anti diabetic activity of Albizia procera in Indian traditional medicine for Diabetes mellitus treatment. The anti hyperglycemic action attributed to the presence of valuable flavonoids, terpinoids in the fraction E.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words: &lt;/strong&gt;&lt;em&gt;Albizia procera&lt;/em&gt;, &lt;em&gt;hyperglycemia&lt;/em&gt;, Streptozocin (STZ).&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Praveen kumar P&lt;sup&gt;*&lt;/sup&gt;, Ramesh A&lt;sup&gt;1&lt;/sup&gt; and Prasad K&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;2&lt;/strong&gt;&lt;/sup&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Vishnu Institute of Pharmaceutical Education &amp;amp; Research,Vishnupur, Narsapur, Medak&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;*,2&lt;/sup&gt;Shri Vishnu college of Pharmacy, Bhimavaram, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Swati Vyas</style></author><author><style face="normal" font="default" size="100%">Sumita Kachhwah</style></author><author><style face="normal" font="default" size="100%">S.L. Kothari</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative analysis of phenolic contents and total antioxidant capacity of Moringa oleifera Lam.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">oxidation</style></keyword><keyword><style  face="normal" font="default" size="100%">sequential extract</style></keyword><keyword><style  face="normal" font="default" size="100%">total flavonoid content</style></keyword><keyword><style  face="normal" font="default" size="100%">total phenolic content</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">27th Nov, 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">44-51</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Accumulation of reactive species higher than permissible limits in biological systems may lead to various degenerative disorders due to oxidative damage.&lt;strong&gt; Materials and Methods: &lt;/strong&gt;Oxidation is a serious concern faced by the food industry causing deterioration of shelved-food quality. Antioxidant compounds like polyphenolics scavenge such free radicals and thus protect against oxidative stress. Consumption of polyphenol-rich plants as dietary component confers protection against such cellular damage. Present study explores antioxidant capacity, total phenolic content (TPC) and total flavonoid content (TFC) of different extracts prepared from various parts of &lt;em&gt;Moringa oleifera&lt;/em&gt; Lam. &lt;strong&gt;Results: &lt;/strong&gt;Higher TPC, TFC and antioxidant activity was shown by methanolic extracts followed by aqueous, petroleum benzene and chloroform extracts. The present study suggests that all the extracts might act as radical scavengers to certain extent possibly due to presence of polyphenolic compounds. &lt;strong&gt;Conclusion: &lt;/strong&gt;&lt;em&gt;M. oleifera&lt;/em&gt; exhibits strong antioxidant activity and could serve as prospective source of natural antioxidants to food and health industries.&lt;/p&gt;&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt;&amp;nbsp; Antioxidant activity, total phenolic content, total flavonoid content, sequential extract, oxidation.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><custom1><style face="normal" font="default" size="100%">Swati Vyas, Sumita Kachhwaha and S.L.Kothari</style></custom1><section><style face="normal" font="default" size="100%">44</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Swati Vyas&lt;sup&gt;1&lt;/sup&gt;, Sumita Kachhwaha&lt;sup&gt;1&lt;/sup&gt; and S.L.Kothari&lt;sup&gt;1,2&lt;/sup&gt;&lt;sup&gt;*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align:justify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Botany, University of Rajasthan, Jaipur, Rajasthan, India&amp;ndash;302004&lt;/p&gt;&lt;p style=&quot;text-align:justify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Institute of Biotechnology, Amity University, Rajasthan, Jaipur, Rajasthan, India-302019&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Janna Vladimirovna Daironas</style></author><author><style face="normal" font="default" size="100%">Fatima Kazbekovna Serebryanaya</style></author><author><style face="normal" font="default" size="100%">Ifrat Nazimovich Zilfi karov</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative Morphological and Anatomical Study of Onosma caucasica Levin. ex M. Pop. and Onosma sericea Willd. (Boraginaceae Juss.)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anatomy</style></keyword><keyword><style  face="normal" font="default" size="100%">Boraginaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Morphology</style></keyword><keyword><style  face="normal" font="default" size="100%">Onosma</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2nd July 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">22-28</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Finding sources of drugs among the species of genus &lt;em&gt;Onosma&lt;/em&gt; of the local fl ora is actual direction. Many of the species of genus &lt;em&gt;Onosma&lt;/em&gt; are weeds, some live exclusively on dry sandy or rocky slopes. Many of the species of genus &lt;em&gt;Onosma&lt;/em&gt; have used in ethnopharmacology as anti-infl ammatory, analgesic, and wound health remedies. The purpose of this research is morphological and anatomical study of herbs of &lt;em&gt;Onosma caucasica&lt;/em&gt; Levin. ex M. Pop. and &lt;em&gt;Onosma sericea&lt;/em&gt; Willd. (Boraginaceae). &lt;strong&gt;Materials and Methods:&lt;/strong&gt; The objects of the study were collected in North Caucasus (Russia) in June 2011. Materials morphological study herbarium specimens were stored in the herbarium fund the Department of Botany (acronym PGFA). Materials micromorphological study were temporary slides are the leaf, stem and fl owers. &lt;strong&gt;Results:&lt;/strong&gt; The morphological results were compared with the Flora of the USSR. Anatomical characters of leaves and stems of the species were observed to be similar to the usual features of Boraginaceae anatomy. All results are supported by photographs. The nature of trichomes on the leaf blade has a major diagnostic value in determining the authenticity of herbs the studied species. &lt;strong&gt;Conclusion:&lt;/strong&gt; The severity of downy leaf blade and the corolla, and the structure of the hair can reliably identify this type of raw material and serve as the basis for the development of the regulatory documentation for its standardization.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Anatomy, Boraginaceae, morphology, &lt;em&gt;Onosma&lt;/em&gt;.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Janna Vladimirovna Daironas&lt;sup&gt;1*&lt;/sup&gt;, Fatima Kazbekovna Serebryanaya&lt;sup&gt;1&lt;/sup&gt;, Ifrat Nazimovich Zilfi karov&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;2&lt;/strong&gt;&lt;/sup&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy and Department of Botany, Pyatigorsk Medical and Pharmaceutical Institute, a Branch of Volgograd State Medical University Ministry of Health of Russian Federation, Pyatigorsk, 357532, Kalinina 11, Russia,&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Phytochemistry, The State Scientifi c Institution the All-Russia Scientifi c Research Institute of Medicinal and Aromatic Plants (VILAR), Moscow, Grin Str. 7, Russia.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sharada L. Deore</style></author><author><style face="normal" font="default" size="100%">Sharad Chaudhari</style></author><author><style face="normal" font="default" size="100%">Bhushan A. Baviskar</style></author><author><style face="normal" font="default" size="100%">Somshekhar S. Khadabadi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Development and Antifungal Evaluation of Cinnamaldehyde Containing Silver Nanoparticles against Candida albicans</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Letter to the Editor</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2nd July 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">63-65</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p &gt;NA&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Letter To The Editor</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Sharada L. Deore&lt;sup&gt;1*&lt;/sup&gt;, Sharad Chaudhari&lt;sup&gt;1&lt;/sup&gt;, Bhushan A. Baviskar&lt;sup&gt;1&lt;/sup&gt;, Somshekhar S. Khadabadi&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;2 &lt;/strong&gt;&lt;/sup&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmacognosy and Phytochemistry, Government College of Pharmacy, Amravati, Maharashtra, India,&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacognosy and Phytochemistry, Government College of Pharmacy, Aurangabad, Maharashtra, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ananth Kumar Kammalla,</style></author><author><style face="normal" font="default" size="100%">Mohan Kumar Ramasamy,</style></author><author><style face="normal" font="default" size="100%">Agarwal Aruna,</style></author><author><style face="normal" font="default" size="100%">Dubey GP,</style></author><author><style face="normal" font="default" size="100%">Ilango Kaliappan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Development and validation of a RP-HPLC method for the simultaneous determination of Mangiferin, Ellagic acid and Hydroxycitric acid in polyherbal formulation</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Ellagic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Hydroxycitric acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Mangiferin</style></keyword><keyword><style  face="normal" font="default" size="100%">Polyherbal formulation</style></keyword><keyword><style  face="normal" font="default" size="100%">RP-HPLC</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">8th April 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">23-28</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;The US patented polyherbal formulation for the prevention and management of Type II diabetes and its vascular complications was used for the present study. The formulation consists of roots of &lt;em&gt;Salacia species&lt;/em&gt;, leaves of &lt;em&gt;Lagestroemia parviflora&lt;/em&gt; and fruit rind of &lt;em&gt;Garcinia indica&lt;/em&gt;. The use of reversed phase C&lt;sub&gt;18&lt;/sub&gt; HPLC column was used and eluted with isocratic mobile phase of acetonitrile and phosphoric acid buffer solution enabled the efficient separation of chemical markers within 20min. Validation of the method was performed in order to demonstrate its selectivity, accuracy, precision, repeatability and recovery. All calibration curve shows good linear correlation coefficients (r&lt;sup&gt;2&lt;/sup&gt;&amp;gt;0.995) within tested ranges. Three markers in this polyherbal formulation were quantified were Mangiferin (1.53% w/w), Ellagic acid (0.9655 w/w), Hydroxycitric acid (5.3% w/w). Intra and inter day RSDs of retention times and peak areas were less than 3%. The recoveries were between 95% and 102.5%. In conclusion a method has been developed for the simultaneous quantification of three markers in this polyherbal formulation. The established RP-HPLC method was simple, precise and accurate and can be used for the quality control of the raw materials as well as formulations.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Polyherbal formulation, Mangiferin, Ellagic acid, Hydroxycitric acid, RP-HPLC.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ananth Kumar Kammalla&lt;sup&gt;1&lt;/sup&gt;, Mohan Kumar Ramasamy&lt;sup&gt;1&lt;/sup&gt;, Agarwal Aruna&lt;sup&gt;2&lt;/sup&gt;, Dubey GP&lt;sup&gt;3&lt;/sup&gt; and Ilango Kaliappan&lt;sup&gt;1*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Interdisciplinary School of Indian System of Medicine, SRM University, Kattankulathur-603203, Tamil Nadu, India&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;National Facility for Tribal &amp;amp; Herbal Medicine, Institute of Medical sciences, Banaras Hindu University, Varanasi, India&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Faculty of Ayurveda, Institute of Medical sciences, Banaras Hindu University, Varanasi, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Natesh Prabhu</style></author><author><style face="normal" font="default" size="100%">Sanjay Hadigal</style></author><author><style face="normal" font="default" size="100%">Ullal sheetal D</style></author><author><style face="normal" font="default" size="100%">Sushma DS</style></author><author><style face="normal" font="default" size="100%">Ashok Shenoy K</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Tribulus Terrestris on Learning And Memory in Wistar Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Hebb William Maze</style></keyword><keyword><style  face="normal" font="default" size="100%">Learning</style></keyword><keyword><style  face="normal" font="default" size="100%">Memory</style></keyword><keyword><style  face="normal" font="default" size="100%">T Maze</style></keyword><keyword><style  face="normal" font="default" size="100%">Tribulus terrestris</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">26th May 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">68-71</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objectives: &lt;/strong&gt;The present study was designed to evaluate the effect of aqueous extract of fruits of &lt;em&gt;Tribulus terrestri&lt;/em&gt;s on learning and memory in rodents. &lt;strong&gt;Materials and methods:&lt;/strong&gt; Thirty wistar rats were divided in 5 groups of 6 rats each. Baseline values for the time taken to reach reward chamber (TRC) in the Hebb William Maze and transfer latency (TL) in the T-maze were recorded on Day 1. Mean of 5 sessions was calculated for each rat. Group I was normal control, group II piracetam standard, group III, IV and V received &lt;em&gt;Tribulus terrestris&lt;/em&gt; orally at 100mg/kg, 200mg/kg and 400mg/kg respectively for 14 days. At the end of 14 days, each rat was tested for TRC and TL and compared with the control group. &lt;strong&gt;Results:&lt;/strong&gt; Group IV showed a significant decrease in TRC when compared to group I in Hebb William Maze (p&amp;lt;0.0001). Group IV also showed a significant decrease in TL when compared to group I in T-maze (p&amp;lt;0.0001). Group III showed a significant decrease in TL when compared to group I in the T-maze (p=0.035), however there was no decrease in TRC in this group.&lt;strong&gt; Conclusion: &lt;/strong&gt;The aqueous extract of fruits of &lt;em&gt;Tribulus terrestris&lt;/em&gt; showed a dose dependent beneficial effect in learning and memory models in rats, with 200mg/kg being most beneficial.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Hebb William Maze, Learning, Memory, T Maze, &lt;em&gt;Tribulus terrestris&lt;/em&gt;&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Natesh Prabhu, Sanjay Hadigal, Ullal Sheetal D&lt;sup&gt;*&lt;/sup&gt;, Sushma DS and Ashok Shenoy K&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Pharmacology, Kasturba Medical College, Light House Hill Road, Mangalore-575001, Manipal University, Manipal, Karnataka, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">D R Kar</style></author><author><style face="normal" font="default" size="100%">G Ghosh</style></author><author><style face="normal" font="default" size="100%">P K Sahu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Estrogenic Effect of Methanolic Extract of Avicennia alba Blume. Aerial Parts in Female Wistar Albino Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Avicennia alba</style></keyword><keyword><style  face="normal" font="default" size="100%">contraceptive</style></keyword><keyword><style  face="normal" font="default" size="100%">Estrogenic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Uterus</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">26th May 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">53-58</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objectives:&lt;/strong&gt; To investigate the estrogenic effect of &lt;em&gt;Avicennia alba&lt;/em&gt; (Blume) aerial parts as identified in the folklore recipes as a contraceptive&lt;strong&gt; Methodology: &lt;/strong&gt;The estrogenic activity study of the methanolic extract was carried out by studying the histopathology of the uterus. The uterine weight and vaginal cornification were also observed. The diameter of uterus, thickness of endometrium and height of the endometrial epithelium were measured using a calibrated ocular micrometer. The estimation of total protein and cholesterol was carried out using a standard method described by Lowely et al. &lt;strong&gt;Results:&lt;/strong&gt; The presence of alkaloids, anthraquinone glycosides, flavonoids, steroids, polyphenolics were detected in the aerial parts of Avicennia alba. The methanolic extract of &lt;em&gt;Avicennia alba&lt;/em&gt; at 400 mg/kg body weight showed a significant (&lt;em&gt;p&lt;/em&gt;&amp;lt; 0.05) increase in uterine weight, diameter of uterus, thickness of endometrium and height of the endometrial epithelium compared to the control. There was increase in vaginal cornification status. The histological examination of the uterus also showed estrogenic influence. A significant increase (&lt;em&gt;p&lt;/em&gt;&amp;lt; 0.05) in total protein and cholesterol content in the uterus of standard and test drug treated rats was also observed.&lt;strong&gt; Conclusion:&lt;/strong&gt; The methanolic extract of &lt;em&gt;Avicennia alba&lt;/em&gt; at 400 mg/kg body weight showed significant estrogenic activity and the results are in consistent with the folkloric claim reports related to oral contraceptive effect of &lt;em&gt;Avicennia alba&lt;/em&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt;&lt;em&gt;Avicennia alba&lt;/em&gt;, contraceptive, estrogenic activity, uterus.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;D R Kar&lt;sup&gt;1*&lt;/sup&gt;, G Ghosh&lt;sup&gt;1&lt;/sup&gt; and P K Sahu&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;1&lt;/strong&gt;&lt;/sup&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1*&lt;/sup&gt;School of Pharmaceutical Sciences, Siksha &amp;lsquo;O&amp;rsquo; Anusandhan University, Bhubaneswar, Odisha-751030, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Noor Kamil</style></author><author><style face="normal" font="default" size="100%">Hafi z Syed Imran-ul-Haque</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hepatoprotective Effect of Calotropis procera in Isoniazid and Rifampicin Induced Hepatotoxicity</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Calotropis procera</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatoprotective</style></keyword><keyword><style  face="normal" font="default" size="100%">isoniazid</style></keyword><keyword><style  face="normal" font="default" size="100%">rifampicin</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2nd July 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">9-14</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; In this study anti-tubercular drugs (isoniazid and rifampicin) induced liver toxicity has been studied for the hepatoprotective effect of hydroethanolic extract of &lt;em&gt;Calotropis procera&lt;/em&gt; (CP) flowers in rats. &lt;strong&gt;Materials and Method:&lt;/strong&gt; Animals were divided into four groups, group Awas given normal saline (1ml/kg), group B received Isoniazid (INH) (50mg/kg) and Rifampicin (RMP)(100mg/kg) group C received INH (50mg/kg), RMP(100mg/kg) and CP(150mg/kg)orally for fourteen days. &lt;strong&gt;Results:&lt;/strong&gt; Biochemical markers of liver toxicity such as AST,ALT,ALP, bilirubin and tissue histology were done inall groups. Anti-Tubercular (Anti-TB) drugs (INH 50mg/kg and RMP100mg/kg) have enhanced the ALT, AST, ALP, bilirubin and histological changes in liver, whereas co-administration of anti-TB drugs with Calotropis procera has reduced these levels within the normal range. &lt;strong&gt;Conclusion:&lt;/strong&gt; Findings of this study showed the hepatoprotective effct of Calotropis Proceraagainst Isoniazid and Rifampicinadministration to reduce the liver damage for chronic treatment.&lt;/p&gt;&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Isoniazid, Rifampicin, &lt;em&gt;Calotropis procera&lt;/em&gt;, Hepatoprotective.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Noor Kamil&lt;sup&gt;1&lt;/sup&gt;, Hafiz Syed Imran-ul-Haque&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;2 &lt;/strong&gt;&lt;/sup&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa 31982-KSA,&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Department of Pharmacology, Dow International Medical College, Dow University of Health Sciences, Karachi-Pakistan.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fernanda P.C. Ribeiro</style></author><author><style face="normal" font="default" size="100%">Hélio M Kamida</style></author><author><style face="normal" font="default" size="100%">Paulo R.M. Almeida</style></author><author><style face="normal" font="default" size="100%">Ana P.T. Uetanabaro</style></author><author><style face="normal" font="default" size="100%">Larissa C.B. Costa</style></author><author><style face="normal" font="default" size="100%">Alexsandro Branco</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Isolation and identification of endophytic fungi in the medicinal plant Mikania laevigata (Asteraceae)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Asteraceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Endophytic fungi</style></keyword><keyword><style  face="normal" font="default" size="100%">Mikania laevigata</style></keyword><keyword><style  face="normal" font="default" size="100%">Xylariaceae</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">26th May 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">10-15</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;The &lt;em&gt;Mikania laevigata&lt;/em&gt; (Asteraceae) is a Brazilian medicinal plant used to treat respiratory tract diseases.It is produced on a large scale for phytotherapic formulation. No studies on the endophytes of &lt;em&gt;Mikania laevigata&lt;/em&gt; have been described in the literature. The endophytic fungi isolated from the leaves of &lt;em&gt;M. laevigata&lt;/em&gt; cultivated in a floral garden located in the south region of the Bahia state, Brazil, were investigated. After surface disinfection, the performing the isolation procedure, a total of forty endophytic fungi were obtained and grouped into different morphospecies. The fungi were characterized by molecular sequencing the ITS rDNA regions, and they were identified by comparing the results published Gen Bank sequences.The phylogenetic analyses revealed four major clades of fungi from the sequenced ITS-rDNA regions: &lt;em&gt;Nodulisporium&lt;/em&gt; sp. (3 isolates), &lt;em&gt;Hypoxylon &lt;/em&gt;sp.(3 isolates), &lt;em&gt;Daldinia&lt;/em&gt; sp. (1isolate) and &lt;em&gt;Xylaria luteo stromata&lt;/em&gt; (aunique isolate).The Xylariaceae Genus was the dominant group of fungi associated with &lt;em&gt;Mikania laevigata&lt;/em&gt;.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt;&amp;nbsp; &lt;em&gt;Mikania laevigata&lt;/em&gt;, Asteraceae, Xylariaceae, Endophytic fungi.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Fernanda P.C. Ribeiro&lt;sup&gt;&amp;ordf;&lt;/sup&gt;, H&amp;eacute;lio M Kamida&lt;sup&gt;b&lt;/sup&gt;, Paulo R.M. Almeida&lt;sup&gt;b&lt;/sup&gt;, Ana P.T. Uetanabaro&lt;sup&gt;c&lt;/sup&gt;, Larissa C.B. Costa&lt;sup&gt;c&lt;/sup&gt; and Alexsandro Branco&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;&amp;ordf;&lt;/strong&gt;&lt;/sup&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;&amp;ordf;&lt;/sup&gt;Laborat&amp;oacute;rio de Fitoqu&amp;iacute;mica, Departamento de Sa&amp;uacute;de, Universidade Estadual de Feira de Santana, Campus Universit&amp;aacute;rio, Av. Transnordestina, s/n&amp;ordm;, Novo Horizonte, 44.036&amp;ndash;900 Feira de Santana, BA, Brazil&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;b&lt;/sup&gt;Laborat&amp;oacute;rio de Pesquisa em Microbiologia, Departamento de Biologia, Universidade Estadual de Feira de Santana,Campus Universit&amp;aacute;rio, Av. Transnordestina, s/n&amp;ordm;, Bairro Novo Horizonte, 44.036&amp;ndash;900 Feira de Santana, BA, Brazil&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;c&lt;/sup&gt;Departamento de Ci&amp;ecirc;ncias Biol&amp;oacute;gicas, Universidade Estadual de Santa Cruz, 45.662&amp;ndash;900 Ilheus, BA,Brazil.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">B. Komuraiah</style></author><author><style face="normal" font="default" size="100%">Srinivas Chinde</style></author><author><style face="normal" font="default" size="100%">A. Niranjana Kumar</style></author><author><style face="normal" font="default" size="100%">K.V.N. Satya Srinivas</style></author><author><style face="normal" font="default" size="100%">Ch. Venu</style></author><author><style face="normal" font="default" size="100%">J. Kotesh Kumar</style></author><author><style face="normal" font="default" size="100%">K.P. Sastry</style></author><author><style face="normal" font="default" size="100%">Paramjit Grover</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Isolation of Phytochemicals From Anticancer Active Extracts of  Syzygium alternifolium Walp. Leaf</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Anticancer activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Epibetulinic acid</style></keyword><keyword><style  face="normal" font="default" size="100%">Eucalyptin</style></keyword><keyword><style  face="normal" font="default" size="100%">Myrtaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Syzygium alternifolium</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">26th May 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">83-85</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective: &lt;/strong&gt;The aim of the present study was to isolate the phyto molecules from the leaf of endemic medicinal pant, &lt;em&gt;Syzygium alternifolium&lt;/em&gt;. The phytochemical investigation of the leaf of the plant yielded a flavonoid Eucalyptin 1 and a triterpinoid Epibetulinic acid 2 in pure state. &lt;strong&gt;Results:&lt;/strong&gt; The compound 1 is being reported for the first time from this plant. The anti-cancer activity showed leaf hexane extract (IC&lt;sub&gt;50&lt;/sub&gt; values 8.177 and 2.687 &amp;micro;g/ml) was significantly active, when compared to extracts and compounds, against human cancer cell lines MCF-7 and DU-145. Also, hexane extract potentially inhibited the growth of DU-145 cell lines when compared with the reference compound doxorubicin. Amongst the isolated compounds, 1 was better cytotoxic than 2. &lt;strong&gt;Conclusion:&lt;/strong&gt; The hexane extract of leaves of &lt;em&gt;S. alternifolium&lt;/em&gt; yielded compounds 1 and 2 and the structure elucidation, based on spectroscopy, revealed them as Eucalyptin and Epibetulinic acid respectively. The compound 1 is being reported for the first time from this plant. The anti-cancer activity showed leaf hexane extract (IC&lt;sub&gt;50&lt;/sub&gt; values 8.177 and 2.687 mg/mL) was significantly active, when compared to extracts and compounds, against human cancer cell lines MCF-7 and DU-145. Also, hexane extract potentially inhibited the growth of DU-145 cell lines when compared with the reference compound doxorubicin. Amongst the isolated compounds, 1 was better cytotoxic than 2.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key Words: &lt;/strong&gt;&lt;em&gt;Syzygium alternifolium&lt;/em&gt;, Myrtaceae, Eucalyptin, Epibetulinic acid, anticancer activity.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;B Komuraiah&lt;sup&gt;1&lt;/sup&gt;, Srinivas Chinde&lt;sup&gt;2&lt;/sup&gt;, A Niranjana Kumar&lt;sup&gt;1&lt;/sup&gt;, K V N Satya Srinivas&lt;sup&gt;1&lt;/sup&gt;, Ch Venu&lt;sup&gt;1&lt;/sup&gt;, J Kotesh Kumar&lt;sup&gt;1*&lt;/sup&gt;, K P Sastry&lt;sup&gt;1&lt;/sup&gt; and Paramjit Grover&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;CSIR-Central institute of Medicinal and Aromatic Plants, Research Centre, Boduppal, Hyderabad-500 092, Andhra Pradesh, India&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Toxicology Unit, Biology Division, CSIR-IICT, Hyderabad, Tarnaka, Hyderabad-500007, Andhra Pradesh, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chuanchom Khuniad</style></author><author><style face="normal" font="default" size="100%">Worathat Thitikornpong</style></author><author><style face="normal" font="default" size="100%">Chanida Palanuvej</style></author><author><style face="normal" font="default" size="100%">Nijsiri Ruangrungsi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic evaluation and chrysazin quantitation of Xyris indica flowering heads</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimicrobial activities</style></keyword><keyword><style  face="normal" font="default" size="100%">Chrysazin</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognostic specification</style></keyword><keyword><style  face="normal" font="default" size="100%">Quantitative analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Xyris indica</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">26th May 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">16-22</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objectives: &lt;/strong&gt;The present study aimed to establish quality specification of &lt;em&gt;Xyris indica&lt;/em&gt; L. flowering heads. The pharmacognostic parameters were investigated. Chrysazin contents were analyzed by TLC image analysis using ImageJ software compared to TLC-densitometry. &lt;strong&gt;Methods: &lt;/strong&gt;&lt;em&gt;X. indica&lt;/em&gt; flowering heads from 15 different sources in Thailand were collected. Morphological and physicochemical parameters were characterized. Chrysazin was successively extracted and determined by TLC image analysis using ImageJ software and TLC-densitometry. &lt;strong&gt;Results:&lt;/strong&gt; Macroscopic study was illustrated as whole plant drawing. The microscopic study showed fragment of corolla, seeds, pollen grain and staminode. The pharmacognostic parameters revealed that the loss on drying, total ash, acid-insoluble ash and water content should be not more than 6.90, 2.50, 0.41, and 11.12 of % dry weight respectively while water and ethanol-soluble extractive values should be not less than 6.59 and 4.03 of % dry weight respectively. TLC fingerprint revealed clearly chrysazin yellow fluorescent band at 365 nm. Chrysazin quantitation by TLC image analysis and TLC densitometry were developed and validated. Chrysazin content was 0.022 &amp;plusmn; 0.001 % dry weight by both methods. There was no statistically significantly difference between these methods. &lt;strong&gt;Conclusion: &lt;/strong&gt;This study provided pharmacognostic specification and chrysazin content of &lt;em&gt;X. indica&lt;/em&gt; flowering heads that can be used for basic quality control and standardization of plant material. TLC image analysis using ImageJ software showed reliable and convenient for analysis of chrysazin content in this crude drug.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words: &lt;/strong&gt;&lt;em&gt;Xyris indica&lt;/em&gt;, Pharmacognostic specification, Chrysazin, Quantitative analysis, Antimicrobial activities&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Chuanchom Khuniad&lt;sup&gt;a&lt;/sup&gt;, Worathat Thitikornpong&lt;sup&gt;b&lt;/sup&gt;, Chanida Palanuvej&lt;sup&gt;a*&lt;/sup&gt; and Nijsiri Ruangrungsi&lt;sup&gt;a,c&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;a&lt;/sup&gt;College of Public Health Sciences, Chulalongkorn University, Bangkok-10330, Thailand&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;b&lt;/sup&gt;Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok-10330, Thailand&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;c&lt;/sup&gt;Faculty of Pharmacy, Rangsit University, Pathumthani-12000, Thailand.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zlatina Kokanova-Nedialkova</style></author><author><style face="normal" font="default" size="100%">Paraskev T. Nedialkov</style></author><author><style face="normal" font="default" size="100%">Stefan D. Nikolov</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic investigations of the aerial parts of Chenopodium foliosum Asch. and radical-scavenging activities of five flavonoids isolated from methanol extract of the plant</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ABTS</style></keyword><keyword><style  face="normal" font="default" size="100%">Chenopodium</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">Flavonoids</style></keyword><keyword><style  face="normal" font="default" size="100%">phytochemical investigations</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">26th May 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">43-48</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background: &lt;/strong&gt;&lt;em&gt;Chenopodium foliosum&lt;/em&gt; Asch. also known in Bulgarian folk medicine as &amp;ldquo;garliche&amp;rdquo; or &amp;ldquo;svinski yagodi&amp;rdquo; (swine&amp;rsquo;s berries) has been used as a decoct of aerial parts for treatment of cancer, as antioxidant and immunostimulant. This study was undertaken to investigate its phytochemical, physicochemical and radicalscavenging activities of the aerial parts of the plant. &lt;strong&gt;Materials and Methods:&lt;/strong&gt; Physico-chemical parameters: moisture content, foaming index, total ash, dichloromethane, alcohol and water soluble extractive, pleliminary phytochemical screening and TLC finger print profile were determined. Three new flavonol glycosides, 3-&lt;em&gt;O-&amp;szlig&lt;/em&gt;;-gentiobiosides of 6-methoxykaempferol andg omphrenol and a new gomphrenol trioside as well as the known 3-&lt;em&gt;O-&amp;szlig&lt;/em&gt;;-gentiobiosides of patuletin and spinacetin, previously isolated from the aerial parts of &lt;em&gt;Chenopodium foliosum&gt; Asch&lt;/em., were analyzed for radical-scavenging activity using DPPH-, ABTS- free radicals. &lt;strong&gt;Results: &lt;/strong&gt;The results of physico-chemical parameters showed moisture content- 6.05%, foaming index-250, total ash- 12.19% and dichloromethane, alcohol and water soluble extractive respectively 2.52%, 13.20% and 12.01%. Preliminary phytochemical screening of the aerial parts of C. foliosum reveals the presence of carbohydrates, flavonoids, phytosterols, saponins and alkaloids/ amines. Patuletine-3-O-gentiobioside showed the highest DPPH (95.03 &amp;plusmn; 0.09) and ABTS (87.20 &amp;plusmn; 0.13) activity, compared to Vit C. 6-Methoxykaempferol-3-O-gentiobioside showed significant ABTS (81.09 &amp;plusmn; 0.06) activity, but DPPH activity was lacking. The other flavonoids showed low DPPH activity, but moderate ABTS activity compared with BHT. &lt;strong&gt;Conclusion:&lt;/strong&gt; The results of this study could be useful for correct identification of the plant and further standardization. In addition this study suggesting that the decoction prepared from &lt;em&gt;C. foliosum&lt;/em&gt; could be a potential source of nutraceuticals with radical-scavenging activity.&lt;/p&gt;&lt;p style=&quot;text-align:justify&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt;&lt;em&gt;Chenopodium&lt;/em&gt;, phytochemical investigations, flavonoids, DPPH, ABTS.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Zlatina Kokanova-Nedialkova&lt;sup&gt;*&lt;/sup&gt;, Paraskev T. Nedialkov and Stefan D. Nikolov&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Pharmacognosy, Faculty of Pharmacy, Medical University of Sofia, Dunav str. 2, 1000 Sofia, Bulgaria.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">C.V. Panchal,</style></author><author><style face="normal" font="default" size="100%">Jyotiram A. Sawale,</style></author><author><style face="normal" font="default" size="100%">B. N. Poul,</style></author><author><style face="normal" font="default" size="100%">Khandelwal, K. R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognostic studies of Lagenaria siceraria (Molina) standley fruits</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Bhopla</style></keyword><keyword><style  face="normal" font="default" size="100%">Cucurbitaceae</style></keyword><keyword><style  face="normal" font="default" size="100%">Lagenaria siceraria</style></keyword><keyword><style  face="normal" font="default" size="100%">Pharmacognostic</style></keyword><keyword><style  face="normal" font="default" size="100%">standardization</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">18th Feb,2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">07-11</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt;&lt;em&gt; Lagenaria siceraria&lt;/em&gt; (LS) fruits belonging to Cucurbitaceae family is widely used in Indian traditional medicine for its various medicinal values. As per best of our knowledge there were no pharmacognostical reports, specifically to determine anatomical and other physicochemical standards required for its standardization. &lt;strong&gt;Material and Methods:&lt;/strong&gt; In this study various standardization parameters like macroscopic and microscopic studies, physico-chemical constants, extractive values and preliminary phytochemical screening were studied and reported. &lt;strong&gt;Results:&lt;/strong&gt; Different standardization parameters were reported, which would be of immense use to identify and establish the authenticity of the plant. &lt;strong&gt;Conclusion:&lt;/strong&gt; Preliminary pharmacognostic evaluation of &lt;em&gt;Lagenaria siceraria&lt;/em&gt; fruits can give some useful information, which will be further used for standardization.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Pharmacognostic, Bhopla, Cucurbitaceae, standardization, Lagenaria siceraria.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;C.V. Panchal&lt;sup&gt;a,*&lt;/sup&gt;, Jyotiram A. Sawale&lt;sup&gt;b&lt;/sup&gt;, B. N. Poul&lt;sup&gt;a&lt;/sup&gt; and K.R. Khandelwal&lt;sup&gt;c&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;a&lt;/sup&gt;Maharashtra College of Pharmacy, Nilanga, Dist. Latur (M.S.) PIN-413521&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;b&lt;/sup&gt;IES College of Pharmcy, Kalkheda Ratibad Main Road, Bhopal (M.P.) PIN-462001&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;c&lt;/sup&gt;Rajarshi Shahu College of Pharmacy and Research, Tathwade, Pune-33 (M.S.)&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Harita Parikh</style></author><author><style face="normal" font="default" size="100%">Aparna Khanna</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Pharmacognosy and Phytochemical Analysis of Brassica juncea Seeds</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Fourier Transform Infrared Spectroscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">High performance Thin layer Chromatography</style></keyword><keyword><style  face="normal" font="default" size="100%">microscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">Phenolics</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2nd July 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">47-54</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt;&lt;em&gt;Brassica juncea&lt;/em&gt; is an economically important plant that has been well-known in India for centuries for its medicinal and nutritive values. The broad spectrum of beneficial effects of the seeds perceived with this plant warrants further exploration of &lt;em&gt;B. juncea&lt;/em&gt; seeds as a potential source for obtaining pharmacologically standardized phytotherapeutics, which could be potentially useful. The objective of the present study was to perform the pharmacognosy of mustards seeds inclusive of qualitative and quantitative phytochemical analysis, fingerprinting by infrared spectroscopy and high performance thin layer chromatography analysis and toxicity assessment &lt;em&gt;in vitro&lt;/em&gt;. &lt;strong&gt;Methods: &lt;/strong&gt;Different sections of seeds were taken and stained with 0.1% phloroglucinol for microscopic examination. The seeds were extracted by 80% alcohol on a rotary shaker to perform phytochemical analysis and fingerprinting. The toxicity assessment of this extract was performed on human dermal fibroblast cells. &lt;strong&gt;Results:&lt;/strong&gt; Microscopic examination of seeds showed characteristic features of mustard seeds. The extraction of these seeds by 20% alcohol resulted in IC&lt;sub&gt;50&lt;/sub&gt; value of 103 &amp;plusmn; 3 &amp;mu;g/mL for 2,2-diphenyl-1-(2,4,6-trinitrophenyl) hydrazyl radical scavenging assay. The fingerprinting analysis of this extract indicated probable presence of sinigrin, quercetin, vanillin, catechin, vitamin E and sulfur-containing compounds. This extract exhibited 50% toxicity (IC&lt;sub&gt;50&lt;/sub&gt;) at 1.79 mg/mL. &lt;strong&gt;Conclusion:&lt;/strong&gt; The result achieved will be used to assess the therapeutic efficacy of seed extracts for future pharmacological evaluations.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Antioxidant, cytotoxicity, Fourier transform infrared spectroscopy, high performance thin layer chromatography, microscopy, phenolics.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Harita Parikh, Aparna Khanna&lt;sup&gt;*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Biological Sciences, School of Science, NMIMS University, Vile Parle (West), Mumbai, Maharashtra, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ponnam Devendar</style></author><author><style face="normal" font="default" size="100%">K.V.N. Satya Srinivas</style></author><author><style face="normal" font="default" size="100%">J. Kotesh Kumar</style></author><author><style face="normal" font="default" size="100%">T. Sandeep Kumar</style></author><author><style face="normal" font="default" size="100%">Savita Bhagel</style></author><author><style face="normal" font="default" size="100%">K.P. Sastry</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phytochemical Investigation, Antioxidant and Antifungal Activities of Rhizomes of Euphorbia Fusiformis</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antifungal activity</style></keyword><keyword><style  face="normal" font="default" size="100%">antioxidant activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Coumarins</style></keyword><keyword><style  face="normal" font="default" size="100%">Euphorbia fusiformis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">26th May 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">78-82</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; Isolation of compounds from &lt;em&gt;Euphorbia fusiformis&lt;/em&gt; rhizomes and evaluation of extracts and each isolates for its antioxidant and antifungal activities.&lt;strong&gt; Results:&lt;/strong&gt; Five compounds were isolated including Euphol 1, &amp;beta;-Sitosterol 2, Caudicifolin 3, Scoparone 4 and Scopoletin 5. The occurrence of the compounds 2, 4 and 5 in the herb reported here for the first time. The ethyl acetate extract showed significant antioxidant activity (IC&lt;sub&gt;50&lt;/sub&gt; = 2.781 mg/ml) and its yielded compound 3 showed moderate antioxidant activity (IC&lt;sub&gt;50&lt;/sub&gt; = 3.25 mg/ml) using DPPH method. The ethyl acetate extract showed better antifungal activity against &lt;em&gt;Aspergillus niger&lt;/em&gt; and &lt;em&gt;Candida albican&lt;/em&gt;s. &lt;strong&gt;Conclusion:&lt;/strong&gt; Compounds&lt;strong&gt; 2, 4, 5 &lt;/strong&gt;were isolated first time from this plant. The ethyl acetate extract showed significant antioxidant and antifungal activity against&lt;em&gt; A. nigar&lt;/em&gt; and &lt;em&gt;C. Albicans&lt;/em&gt;. Thus, this study concludes by demonstrating the isolation, characterization, antioxidant and antifungal properties of &lt;em&gt;E. fusiformis&lt;/em&gt;, which may have further therapeutic value.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key Words:&lt;/strong&gt;&lt;em&gt;Euphorbia fusiformis&lt;/em&gt;, coumarins, antioxidant activity, antifungal activity.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Ponnam Devendar, K V N Satya Srinivas, J Kotesh Kumar,&lt;sup&gt;*&lt;/sup&gt; T Sandeep Kumar, Savita Bhagel and K P Sastry &lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;CSIR-Central Institute of Medicinal and Aromatic Plants-Research Centre, Boduppal, Hyderabad-500092, Telangana State, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">D. R Ch Sekhara Reddy</style></author><author><style face="normal" font="default" size="100%">G Siva Kumar</style></author><author><style face="normal" font="default" size="100%">B. M. Vrushabendra Swamy</style></author><author><style face="normal" font="default" size="100%">K. Phani Kumar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Protective effect of cissampelos pareira linn. Extract on gentamicin-induced nephrotoxicity and oxidative damage in rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cissampelos pareira</style></keyword><keyword><style  face="normal" font="default" size="100%">Creatinine</style></keyword><keyword><style  face="normal" font="default" size="100%">DPPH</style></keyword><keyword><style  face="normal" font="default" size="100%">Gentamicin</style></keyword><keyword><style  face="normal" font="default" size="100%">Glucose</style></keyword><keyword><style  face="normal" font="default" size="100%">Glutathione</style></keyword><keyword><style  face="normal" font="default" size="100%">Lipid peroxidation</style></keyword><keyword><style  face="normal" font="default" size="100%">Reducing power</style></keyword><keyword><style  face="normal" font="default" size="100%">urea</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">26th May 2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">59-67</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; To evaluate the potential nephroprotective and antioxidant activity of hydroalcoholic Cissampelos pareira (&lt;em&gt;C. pareira&lt;/em&gt;) whole plant extract using gentamicin-induced rats. &lt;strong&gt;Methods:&lt;/strong&gt; For studying acute toxicity study, single oral dose of 2g/kg hydroalcoholic extract of &lt;em&gt;C. pareira&lt;/em&gt; was evaluated in rats by oral gavage. The nephroprotective activity was evaluated using gentamicin-induced model in rats. &lt;em&gt;In-vitro&lt;/em&gt; antioxidant activity was evaluated by using DPPH assay and reducing power assay. &lt;em&gt;In-vivo&lt;/em&gt; antioxidant activity was evaluated by using glutathione and lipid peroxidation estimations in gentamicin-induced rats. Hydroalcoholic &lt;em&gt;C. pareira&lt;/em&gt; whole plant extract was given at a dose of 200 and 400 mg/kg p.o. &lt;strong&gt;Results:&lt;/strong&gt; For acute toxicity testing rats administered with the extract at a dose 2 g/ kg. the result showed no toxicity. Hydroalcoholic &lt;em&gt;C. Pareira&lt;/em&gt; whole plant extract (200 and 400 mg/kg p.o) significantly decrease the elevated urinary glucose levels in the urine, decrease the elevated urea and creatinine levels in blood and increase the urinary creatinine levels in gentamicin-induced nephrotoxic rats. The extract had shown significant dose dependent increase in the DPPH and reducing power activity. There were a dose dependent decreasing and increasing of lipid peroxidation, glutathione levels in hydoalcoholic extract treated groups respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; This study exhibits that hydroalcoholic &lt;em&gt;C. pareira&lt;/em&gt; whole plant extract poses nephroprotective activity which may be due to its antioxidant activity.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words: &lt;/strong&gt;Gentamicin, &lt;em&gt;Cissampelos pareira&lt;/em&gt;, creatinine, urea, glucose, lipid peroxidation, glutathione, reducing power, DPPH.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;D. R Ch Sekhara Reddy&lt;sup&gt;1*&lt;/sup&gt;, G. Siva Kumar &lt;sup&gt;2&lt;/sup&gt;, B. M. Vrushabendra Swamy&lt;sup&gt;2&lt;/sup&gt; and K. Phani Kumar&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;1&lt;/strong&gt;&lt;/sup&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Acharya Nagarjuna University College of Pharmaceutical Sciences, Nagarjuna Nagar, Guntur-522510, India&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Gautham College of Pharmacy, Bhuvaneswari Nagar, Bengaluru-560032, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Snehal Suryavanshi,</style></author><author><style face="normal" font="default" size="100%">Anand Zanwar,</style></author><author><style face="normal" font="default" size="100%">Mahabaleshwar Hegde,</style></author><author><style face="normal" font="default" size="100%">Ruchika Kaul-Ghanekar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Standardization of a polyherbal formulation (HC9) and comparative analysis of its cytotoxic activity with the individual herbs present in the composition in breast cancer cell lines</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">HPTLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Physicochemical</style></keyword><keyword><style  face="normal" font="default" size="100%">Phytochemical</style></keyword><keyword><style  face="normal" font="default" size="100%">polyherbal formulation HC9</style></keyword><keyword><style  face="normal" font="default" size="100%">standardization</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">18th Feb,2014</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">6</style></volume><pages><style face="normal" font="default" size="100%">87-95</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The present study aims to standardize a polyherbal formulation (HC9) that was previously shown to exhibit excellent antioxidant and cytotoxic activity in breast cancer cells. Here, we have compared the cytotoxic activity of HC9 with its individual components in breast cancer and non-cancerous cells. &lt;strong&gt;Methods:&lt;/strong&gt; Physico-chemical and phytochemical evaluation of HC9 was performed. Qualitative and quantitative HPTLC analysis of component herbs and HC9 was done by using specific markers. The cytotoxic activity of HC9 with its individual components was evaluated in breast cancer (MCF-7 and MDA MB-231) and non-cancerous cell lines (HEK-293, HaCaT and MCF-10A) by MTT dye uptake.&lt;strong&gt; Results:&lt;/strong&gt; Physico-chemical results revealed that HC9 contained 7.24% total ash content, 9.52% of alcohol-soluble extractive, 0.801 specific gravity, 0.50g/ml bulk density and exhibited 7.18% loss on drying. Phytochemical results revealed the presence of alkaloids, carbohydrates, flavanoids, saponins, tannins and phenolic compounds, and absence of terpenoids. The individual herbs of HC9 and the formulation showed the presence of marker compounds such as picroside-I, nootkatone, 6-gingerol, matairesinol, swertiamarin, berberine, connesine and 2-hydroxy-4-methoxybenzaldehyde. At 160&amp;mu;g/ml concentration, HC9 exhibited cytotoxicity in both MCF7 and MDA MB231 with no cytotoxicity in MCF-10A, HaCaT and HEK-293. In contrast, at this concentration, the individual herbs of HC9 exhibited cytotoxicity not only in cancerous cells, but also in non-cancerous cells.&lt;strong&gt; Conclusion:&lt;/strong&gt; These results suggest that the standardized HC9 formulation was safe to non-cancerous cells and exhibited significant antineoplastic potential in breast cancer cells. Thus, HC9 could be a potential drug candidate in breast cancer.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Cytotoxicity, HPTLC, physicochemical, polyherbal formulation HC9, phytochemical, standardization.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">87</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Snehal Suryavanshi, Anand Zanwar, Mahabaleshwar Hegde and Ruchika Kaul-Ghanekar&lt;/strong&gt;&lt;sup&gt;&lt;strong&gt;*&lt;/strong&gt;&lt;/sup&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;Interactive Research School for Health Affairs (IRSHA), Bharati Vidyapeeth University Medical College Campus, Dhankawadi, Pune-Satara Road, Pune-411043, India.&lt;/p&gt;</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sumet Kongkiatpaiboon</style></author><author><style face="normal" font="default" size="100%">Piyanuch Rojsanga,</style></author><author><style face="normal" font="default" size="100%">Virote Pattarajinda,</style></author><author><style face="normal" font="default" size="100%">Wandee Gritsanapan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Acetylcholinesterase inhibitory activity of didehydrostemofoline, stemofoline alkaloids and extracts from Stemona collinsiae Craib roots</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Acetylcholinesterase inhibition</style></keyword><keyword><style  face="normal" font="default" size="100%">Didehydrostemofoline</style></keyword><keyword><style  face="normal" font="default" size="100%">Stemofoline</style></keyword><keyword><style  face="normal" font="default" size="100%">Stemona collinsiae</style></keyword><keyword><style  face="normal" font="default" size="100%">Stemonaceae</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><volume><style face="normal" font="default" size="100%">5</style></volume><pages><style face="normal" font="default" size="100%">56-59</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; Acetylcholinesterase (AChE) inhibition is one of insect toxicity mechanisms found in many plants. &lt;em&gt;Stemona collinsiae&lt;/em&gt; Craib, a traditional insecticidal plant, has been of interest for its AChE inhibitory activity.&lt;strong&gt; Methods:&lt;/strong&gt; Powdered roots of &lt;em&gt;S. collinsiae&lt;/em&gt; were successively extracted with hexane, dichloromethane, and methanol. The contents of major active insecticidal components, didehydrostemofoline and stemofoline alkaloids, were analyzed by HPLC. Anti-AChE activity was evaluated using Ellman&amp;rsquo;s colorimetric method and TLC-bioautography. &lt;strong&gt;Results:&lt;/strong&gt; The contents of didehydrostemofoline and stemofoline alkaloids in the hexane, dichloromethane, and methanol extracts were 3.59 and 0.18, 40.78 and 0.74, and 1.43 and 0.09% w/w, respectively. TLC fingerprints of each extract showed major spots of didehydrostemofoline and stemofoline of which TLC bioassays indicated active AChE inhibitory activity. IC&lt;sub&gt;50&lt;/sub&gt; values on anti-AChE activities of hexane, dichloromethane and methanol extracts were 126.72, 73.78, and &amp;gt;1000 mg/ml, respectively while those of didehydrostemofoline, stemofoline, and standard galanthamine were 131.3, 102.1, and 1.30 mM, respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; The AChE inhibitory activity of hexane, dichloromethane and methanol extracts from &lt;em&gt;S. collinsiae&lt;/em&gt; roots and their major alkaloids, didehydrostemofoline and stemofoline, were determined. The data support the traditional utilization of this plant as a natural insecticide.&lt;/p&gt;&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; Acetylcholinesterase inhibition, Didehydrostemofoline, Stemofoline, &lt;em&gt;Stemona collinsiae&lt;/em&gt;, Stemonaceae.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify; &quot;&gt;&lt;strong&gt;Sumet Kongkiatpaiboon&lt;sup&gt;a&lt;/sup&gt;, Piyanuch Rojsanga&lt;sup&gt;b&lt;/sup&gt;, Virote Pattarajinda&lt;sup&gt;c&lt;/sup&gt;, Wandee Gritsanapan&lt;sup&gt;a,*&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p style=&quot;text-align: justify; &quot;&gt;&lt;sup&gt;a&lt;/sup&gt;Department of Pharmacognosy, Faculty of Pharmacy, Mahidol University, 447 Sri-Ayutthaya Rd, Ratchathewi, Bangkok 10400, Thailand&lt;/p&gt;&lt;p style=&quot;text-align: justify; &quot;&gt;&lt;sup&gt;b&lt;/sup&gt;Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Mahidol University, Bangkok 10400, Thailand&lt;/p&gt;&lt;p style=&quot;text-align: justify; &quot;&gt;&lt;sup&gt;c&lt;/sup&gt;Department of Animal Science, Faculty of Agriculture, Khon Kaen University, Khon Kaen 40002, Thailand&lt;/p&gt;</style></auth-address></record></records></xml>