ArticleViewAbstractPharmacognosy Journal,2025,17,6,727-732.DOI:10.5530/pj.2025.17.91Published:December 2025Type:Original ArticleCytotoxic Activity of Annona Muricata L, Momordica Charantia L. and Launaea Taraxacifolia Willd. from Benin: A Flow Cytometric ApproachHabib Ganfon, Axel Ahouansou, Celia Dechavanne, Callinice Capo-Chichi, Latifou Lagnika, Agnes Aubouy, Sebastien Dechavanne, and Achille Massougbodji Habib Ganfon1*, Axel Ahouansou1,2,3,4, Célia Dechavanne2,5, Callinice Capo- Chichi3, Latifou Lagnika4, Agnès Aubouy2,6, Sébastien Dechavanne2,5, Achille Massougbodji2 1Laboratoire de Pharmacognosie et Phytothérapie du Centre de Recherche et de Développement du Médicament (CRDM-PharmaLab), 01 BP 188, Université d’Abomey-Calavi (UAC), BENIN 2Institut de Recherche Clinique du Benin (IRCB), 04 BP 1114, Abomey-Calavi, BENIN 3Laboratoire de recherche sur les Biomarqueurs Moléculaires en Cancérologie et en Nutrition, Unité de Biochimie et Biologie Moléculaire UAC, BENIN 4Laboratoire de Biologie Intégrative pour l’Innovation Thérapeutique, Unité de Biochimie et des Substances Naturelles Bioactives, UAC, BENIN 5IRD, Inserm, MERIT, Université Paris Cité, F-75006 Paris, FRANCE 6UMR 152 PHARMADEV, IRD, Université de Toulouse, FRANCE Abstract:Background: Cancer is rising worldwide, causing approximately 9.7 million deaths in 2022. Treatments are costly, have significant side effects, and are sometimes unavailable in Benin. Medicinal plants offer promising avenues for new therapeutic agents. Objective: This study uses flow cytometry method to evaluate the cytotoxic activity of Annona muricata (Annonaceae), Momordica charantia (Cucurbitaceae) and Launaea taraxacifolia (Asteraceae), three plants from the Beninese pharmacopoeia known for their anti-cancer properties. Materials and Methods: The leaves of A. muricata, L. taraxacifolia and whole plants of M. charantia were collected in southern Benin. Extracts were prepared by aqueous decoction and sequential extraction with solvents of increasing polarity (dichloromethane, ethyl acetate, methanol). The phytochemical profiles of the extracts were determined using TLC and tube tests. The cytotoxicity of the extracts was evaluated on THP-1 cancer cells and PBMC healthy cells. After treatment with the extracts, cell viability was measured by flow cytometry after staining with Thiazole Orange and Hoechst 33258. Results: The dichloromethane extracts of A. muricata and M. charantia, and the ethyl acetate extract of M. charantia and L. taraxacifolia showed significant cytotoxic effects on THP-1 cells. Their half-maximal inhibitory concentrations (IC50) were 139.6 μg/mL, 72.89 μg/mL, 81.88 μg/mL and 106.3 μg/ mL, respectively. These extracts also demonstrated good selectivity toward normal cells. Phytochemical screening revealed the presence of alkaloids, coumarins, flavonoids, anthracene glycosides and triterpenes in the active extracts. Conclusion: This study demonstrated the cytotoxic potential of three medicinal plants from the Beninese pharmacopoeia which may serve to develop further new anticancer therapies. Keywords:Benin, Cancer, Cytotoxicity, Plant extracts, selectivity, THP-1 cellsView:PDF (548.68 KB) PDF Images PJ-17-6-2408 ‹ Phytochemical Profile and Bioactivity of Dioscorea transversa R. Br: Antioxidant and Anti-Inflammatory Potential of Leaf and Tuber up Microscopic Standardization and Bioactive Profiling of Cissampelos pareira Roots ›