COMPARATIVE IN-VITRO ANTICANCER EFFICACY EVALUATION: CASSIA ABBREVIATE MEDIATED COPPER-DOPED MAGNESIUM OXIDE NANOPARTICLES VSCRUDE AQUEOUS BARK EXTRACT.
AbstractBackground: In Zimbabwe, green synthesis of nanoparticles has recently drawn much attention due to its eco-friendliness, biocompatibility, and capability to augment the healing properties of medicinal plants. Cassia abbreviata (Muremberembe) is a cardinal Zimbabwean traditional medicinal plant used to manage various conditions. However, there is limited scientific evidence on the antiproliferative activity of both C. abbreviata extracts and C. abbreviata-mediated nanoparticles against cancer cell lines. Therefore, this study compared the in-vitro antiproliferative efficacy of an aqueous bark extract of C. abbreviata and biosynthesized copper-doped magnesium oxide nanoparticles mediated by C. abbreviata against the human breast cancer cell line HCC1937. Methods: Cytotoxicity assays were performed using the well-known and standardized Sulforhodamine B (SRB) colorimetric assay method over a concentration range (1). IC50 values were calculated using dose-response curve trend-line equations. Results: Both treatments significantly inhibited proliferation of HCC1937 breast cancer cells in a concentration-dependent manner (P < 0.0001). Cu₂O–MgO NPs showed higher antiproliferative activity than the aqueous bark extract with a lower IC₅₀ value (35.08 μg/mL vs. 61.43 μg/mL). Conclusion: Cassia abbreviata-mediated Cu₂O–MgO nanoparticles demonstrated significantly greater antiproliferative activity than the crude aqueous bark extract against HCC1937 breast cancer cells, highlighting their potential as promising candidates for further anticancer development.
Article Information
33
3214-3220
515 KB
6
English
IJPSR
T. Jakata* and J. Chifamba
Department of Pharmacy and Pharmaceutical Sciences, University of Zimbabwe, P O Box MP617, Mt Peasant, Harare, Zimbabwe.
tinashehj@gmail.com
11 June 2026
18 July 2026
25 September 2026
10.13040/IJPSR.0975-8232.17(10).3214-20
01 October 2026





