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dc.contributor.authorDenis Mabeya Ogato, Eliakim Mbaka Mauti, Godfrey Omare Mauti, Barasa Ambrose, David Keno
dc.date.accessioned2022-10-09T13:15:54Z
dc.date.available2022-10-09T13:15:54Z
dc.date.issued2015
dc.identifier.issn2230-480X
dc.identifier.urihttps://repository.maseno.ac.ke/handle/123456789/5385
dc.descriptionOnline at: www.phytopharmajournal.comen_US
dc.description.abstractCancer is a life-threatening disease and leads to high rates of mortality worldwide, after cardiovascular disease, is the second leading cause of death. Investigations for finding new plant based anticancer compounds are imperative and interesting. There are many studies on anticancer herb/plant extracts in cell line models. Eugenia jambolana has been reported to contain phytochemicals like coumarin, flavanoids, glycosides, phenols, tannins and steroids. The various part of Eugenia jambolana have therapeutic applications. Plant active components were extracted using the decoction extraction method and the filtrate was obtained by means of filtering through a Whattman no.1 filter paper. The filtrate was evaporated in a weighed flask in a hot air oven set at 50°C. Extracts were reconstituted by re-dissolving in respective solvents. Different concentration i.e. 8, 15.6, 31.25, 62.5, 125, 250, 500 and 1000 µg. of the plant extracts were tested for the anticancer activity. The anticancer assay was performed on Human laryngeal epithiloma cells (Hep 2) obtained from King Institute of Preventive Medicine, Chennai, India. The cell viability was measured using MTT assay. Controls were maintained throughout the experiment (Untreated wells as cell control and diluent treated wells as diluent control). The assay was performed in triplicates for each of the extracts.en_US
dc.publisherResearchGateen_US
dc.subjectEugenia jambolana, Human laryngeal epithiloma cells (Hep2), MTT assay, Anticanceren_US
dc.titleAnticancer activity of Eugenia jambolana seeds against Hep2 cell linesen_US
dc.typeArticleen_US


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