COMPARATIVE IN VITRO ANTICANCER ACTIVITY OF METHANOLIC EXTRACT OF TRADITIONALLY USED MEDICINAL PLANT OF MIZORAM
Objective: The main objective was to find out the in vitro comparative anticancer activity of various methanolic extract. Methods: Plants samples such as Mikania micrantha, Allium hookeri, Eryngium foetidium, and Alpinea galanga were collected, identified and authenticated. By using Trypan blue test...
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Veröffentlicht in: | International journal of current pharmaceutical research 2019-07, p.84-87 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Objective: The main objective was to find out the in vitro comparative anticancer activity of various methanolic extract.
Methods: Plants samples such as Mikania micrantha, Allium hookeri, Eryngium foetidium, and Alpinea galanga were collected, identified and authenticated. By using Trypan blue test Human cervical cancer (Hela) cells were counted. TheHuman cervical cancer (Hela) cells were treated with methanolic extract of Mikania micrantha, Allium hookeri, Eryngium foetidium and Alpinia galanga.20 µl of MTT (5 mg/ml) solution was added to cells per well, and the plate was moved to a cell incubator. Measurement was performed using a Spectramax M2 Microplate Reader (Molecular Diagnostic, Inc.) at a wavelength of 570 nm.
Results: The Cytotoxicity of studied medicinal plants of Mizoram such as Mikania micrantha, Allium hookeri, Eryngium foetidium and Alpinia galanga exhibited cytotoxicity in an increased manner with increase concentration against Hela cells. Their IC50 values were 49.02, 138.5, 199.7 and 209.4 µg ml-1 respectively. The IC50 of doxorubicin was found to be 3.305µg ml-1. The anticancer activity of the leaves related to their content of flavanoids. This study validates the traditional use of plants in the management of cancer.
Conclusion: The Cytotoxicity of studied medicinal plants of Mizoram such as Mikania micrantha, Allium hookeri, Eryngium foetidium and Alpinia galanga exhibited cytotoxicity in an increased manner with increase concentration against HeLa cells. |
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ISSN: | 0975-7066 0975-7066 |
DOI: | 10.22159/ijcpr.2019v11i4.34929 |