<?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%">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%">Dachriyanus</style></author><author><style face="normal" font="default" size="100%">Nova Susanti Asjar</style></author><author><style face="normal" font="default" size="100%">Meri Susanti</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Determination of Rubraxanthone in the Latex of Asam Kandis (Garcinia cowa Roxb) by Reverse Phase High Performance Liquid Chromatography.</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Counterfeiting</style></keyword><keyword><style  face="normal" font="default" size="100%">Isocratic method</style></keyword><keyword><style  face="normal" font="default" size="100%">Latex of Garcinia cowa Roxb</style></keyword><keyword><style  face="normal" font="default" size="100%">RP-HPLC</style></keyword><keyword><style  face="normal" font="default" size="100%">rubraxanthone</style></keyword><keyword><style  face="normal" font="default" size="100%">Standarization</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/317</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">288-291</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; Rubraxanthone is a major compound found in &lt;em&gt;Garcinia cowa&lt;/em&gt; Roxb which has various biological activities. This compound is likely to be responsible for the pharmacological activities of this plant. The latex of this plant was one of the source of this compound. To prevent counterfeiting, it is essential to develop a method of analysis to determine the levels of these compounds in the latex of &lt;em&gt;G. cowa&lt;/em&gt;. &lt;strong&gt;Aims:&lt;/strong&gt; To develop and validated a reverse phase-high performance liquid chromatography (RP-HPLC) technique for determination of rubraxanthone in the latex of &lt;em&gt;G. cowa&lt;/em&gt;. &lt;strong&gt;Settings and Design:&lt;/strong&gt; RP-HPLC analysis. &lt;strong&gt;Methods and Material:&lt;/strong&gt; The sample was powdered and dissolve in methanol and then subjected to Reverse Phase High Performace Liquid Chromatoraphy (RP-HPLC). Separation was carried out in a reversed-phase column Shimadzu Shimp-pack VP&amp;ndash;ODS (4.6 x 250 mm). The elution was performed with isocratic solvent using formic acid 0.4 % v/v in methanol (15:85) with a flow rate 1 ml/minute. The solvents used for the mobile phase were filtered through membrane filter (0.45 mm pore size) and degassed before use. Total running time was 20 minutes and the sample injection volume of injection was 20 ml. While the wavelength of the UV-VIS detector was set at 243.2 nm. &lt;strong&gt;Results:&lt;/strong&gt; The detection and the quantitation limits of rubraxanthone were 1.119 mg/mL and 3.731 &amp;mu;g/mL, respectively. A regression analysis was performed, with the observation of good linearity (r = 0.998). The values obtained for precision and accuracy determination are in agreement with ICH guidelines. It was found that rubraxanthone in dichloromethane extract of latex &lt;em&gt;G. cowa&lt;/em&gt; was 56.56%. &lt;strong&gt;Conclusions:&lt;/strong&gt; The results demonstrated that the developed method is a reliable HPLC technique for determination of rubraxanthone in the latex of &lt;em&gt;G. cowa&lt;/em&gt;.&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%">288</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Dachriyanus*, Nova Susanti Asjar, Meri Susanti &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Department of Andalas University, Kampus Limau Manis, Padang, West Sumatra, 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%">Sajad Hassan Wani</style></author><author><style face="normal" font="default" size="100%">Hilal Ahmad Bhat</style></author><author><style face="normal" font="default" size="100%">Javid Iqbal Mir</style></author><author><style face="normal" font="default" size="100%">Shahid Ali Akbar</style></author><author><style face="normal" font="default" size="100%">Sajad Un Nabi</style></author><author><style face="normal" font="default" size="100%">Desh Beer Singh</style></author><author><style face="normal" font="default" size="100%">Nazeer Ahmad</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Quantitative Analysis of Irigenin in the Different Species of Iris Plant by RP- HPLC and its Efficacy Against Different Plant 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%">Bio efficacy</style></keyword><keyword><style  face="normal" font="default" size="100%">Irigenin</style></keyword><keyword><style  face="normal" font="default" size="100%">Iris Plant</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%">November 2017</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/377</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">s23-s27</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;Irigenin belongs to family of &lt;em&gt;isoflavonoids&lt;/em&gt;, isolated from &lt;em&gt;Iris Plant&lt;/em&gt; of Kashmir Himalaya. A rapid and specific reverse phase high pressure chromatography (RP HPLC) method for quantitative analysis of irigenin in the different species of &lt;em&gt;Iris Plant&lt;/em&gt; was developed. The samples were analyzed on RP-C&lt;sub&gt;18&lt;/sub&gt; e column (chromolith, 5&amp;mu;m, 4.6&amp;times;100 mm). The HPLC system was operated at ambient temperature (&amp;plusmn;30c). The mobile phase consisted of methanol: water. The detecting wavelength at 260 nm and flow rate of 0.6 ml/min. The standard irigenin was diluted using the mobile phase at a known concentration of 1mg/ml; the sample was filtered through sample filter of 0.45 &amp;mu; pore size. The filtrate was introduced on to a reverse phase analytical column. The content of irigenin in the different species of &lt;em&gt;Iris Plant&lt;/em&gt; was determined. The HPLC showed an excellent performance in separating the irigenin in different species of &lt;em&gt;Iris Plant&lt;/em&gt;. Furthermore, the antipathogenic activity. The test compound at each respective concentration was found to be statistically superior against scab. Furthermore, the test compound @ 5000 ppm proved significantly most effective by providing (82.49%) inhibition in the mycelia growth of apple scab. It was followed by fusarium (77.27%) at 5000 ppm. Lowest reduction in mycelia growth (65.78%) was recorded in &lt;em&gt;marssonina&lt;/em&gt; and did not differ significantly from Alternaria (67.47%) at 5000 ppm. Furthermore, lowest inhibition of mycelia growth was recorded at 1000 ppm. Similar trend was recorded for rest of the pathogens i.e. highest reduction at 5000 ppm, lowest at 1000 ppm and at 2000, 3000 and 4000 ppm it ranges between the first two but increases with increase in concentration. From this study irigenin is potent compound which can be used for controlling the growth of respective pathogens.&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%">s23</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Sajad Hassan Wani&lt;sup&gt;1&lt;/sup&gt;*, Hilal Ahmad Bhat&lt;sup&gt;1&lt;/sup&gt;, Javid Iqbal Mir&lt;sup&gt;1&lt;/sup&gt;, Shahid Ali Akbar&lt;sup&gt;2&lt;/sup&gt;, Sajad un Nabi&lt;sup&gt;3&lt;/sup&gt;, Desh Beer Singh&lt;sup&gt;4&lt;/sup&gt;, Nazeer Ahmad&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;Biotechnology division, Central Institute of Temperate Horticulture- ICAR, Srinagar, Jammu and Kashmir, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Entomology division, Central Institute of Temperate Horticulture- ICAR, Srinagar, Jammu and Kashmir, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Plant Pathology, Central Institute of Temperate Horticulture- ICAR, Srinagar, Jammu and Kashmir, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Central Institute of Temperate Horticulture- ICAR, Srinagar, Jammu and Kashmir, INDIA.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Sheri Kashmir University of Agriculture Science and Technology Kashmir (SKUAST-K), Jammu, 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%">Sunita Shailajan</style></author><author><style face="normal" font="default" size="100%">Sasikumar Menon</style></author><author><style face="normal" font="default" size="100%">Dipti Singh</style></author><author><style face="normal" font="default" size="100%">Gauri Swar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Validated analytical RP-HPLC method for quantitation of wedelolactone from Eclipta alba and marketed Ayurvedic formulations</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Eclipta alba</style></keyword><keyword><style  face="normal" font="default" size="100%">Formulations</style></keyword><keyword><style  face="normal" font="default" size="100%">RP-HPLC</style></keyword><keyword><style  face="normal" font="default" size="100%">Validation</style></keyword><keyword><style  face="normal" font="default" size="100%">Wedelolactone.</style></keyword><keyword><style  face="normal" font="default" size="100%">Whole plant</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%">132-139</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;Eclipta alba&lt;/em&gt; Linn. (Asteraceae) is an important ingredient of several Ayurvedic formulations. The monograph on different parts of plant like flowers, leaves, roots are listed in Ayurvedic pharmacopeia of India. The plant is reported to be effective for broad range maladies like inflammation, reproductive problems of females etc. It is also used as a hepatoprotectant, analgesic, antibacterial and antidiabetic agent. Wedelolactone is used as a bioactive marker to establish the quality of the crude drug and its formulations. In the present study, wedelolactone-based standardization of &lt;em&gt;Eclipta alba&lt;/em&gt; and its quantitation from marketed herbal and Ayurvedic formulations has been documented using RP-HPLC. &lt;strong&gt;Methods&lt;/strong&gt;: In the current work, an isocratic method has been developed and validated to quantitate wedelolactone from whole plant of &lt;em&gt;Eclipta alba&lt;/em&gt;. This method is validated as per ICH guidelines and is used to quantitate the content of wedelolactone in polyherbal formulations like Liv52, Geriforte, Mahabhringaraj oil etc. &lt;strong&gt;Results: &lt;/strong&gt;The LOD is found to be 0.5 &amp;mu;g/mL and the LOQ is 1 &amp;mu;g/mL. The linearity range of response is from 5 &amp;mu;g/mL to 100 &amp;mu;g/mL. &lt;strong&gt;Conclusion:&lt;/strong&gt; The validated method is found to be simple, sensitive, accurate, rugged and reproducible. This developed method can be recommended for quality assurance and marker-based standardization of polyherbal formulations containing whole plant of &lt;em&gt;Eclipta alba.&lt;/em&gt;&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%">132</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Sunita Shailajan&lt;sup&gt;1&lt;/sup&gt;, Sasikumar Menon&lt;sup&gt;2&lt;/sup&gt;, Dipti Singh&lt;sup&gt;1&lt;/sup&gt;, Gauri Swar&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, Mumbai - 400 019, India&lt;/p&gt;

&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Institute for Advanced Training and Research in Interdisciplinary Science, Plot No. 194, Scheme No. 6, Road No. 15, Sion Koliwada, Sion (East), Mumbai-400 022, 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></records></xml>