Abstract

Cancer treatments usually cause adverse drug reactions. Therefore, safe anticancer drugs are needed in the treatment of cancer. One source of medicine that can be explored is plant. Extracts of longan leaves (Dimocarpus longan), jamaican cherry leaves (Muntingia calabura), and avocado leaves (Persea americana) have been tested for cytotoxic activity against several cancer cell lines. This study aims to determine the cytotoxic activity of ethanolic extract of longan leaves, jamaican cherry leaves, and avocado leaves against T47D and WiDr cells and to identify secondary metabolites in the extracts which have the highest activity. Ethanolic extract of longan leaves, jamaican cherry leaves, and avocado leaves were tested for their cytotoxic activity using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method. Identification of secondary metabolites in the ethanolic extract of avocado leaves was carried out by thin layer chromatography method using silica gel GF254 as the stationary phase and a mixture of n-hexane and acetone (6:4) as the mobile phase. Cytotoxic test results show that ethanolic extract of longan leaves and cherry leaves with concentration of up to 1600 μg/mL do not reduce the T47D and WiDr living cells to 50%. Avocado leaf extract decreases the percentage of living T47D cells and WiDr with IC50 values of 790.679 µg/mL and 1072.2 µg/mL, respectively. The ethanolic extract of avocado leaves contains flavonoid, phenolic, and terpenoid. Ethanolic extract of longan leaves, cherry leaves and avocado leaves do not have cytotoxic activity against T47D and WiDr cells.

Highlights

  • Cancer treatments usually cause adverse drug reactions

  • This study aims to determine the cytotoxic activity of ethanolic extract of longan leaves, jamaican cherry leaves, and avocado leaves against T47D and WiDr cells and to identify secondary metabolites in the extracts which have the highest activity

  • American Journal of Chinese Medicine, 39(1), pp. 183-200

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Summary

METODE PENELITIAN

Alat yang digunakan dalam penelitian ini adalah autoklaf (Hirayama), oven (Memmert), cytoculture cabinet (ESCO), inkubator CO2. (Binder), mikroskop (Olympus), sonikator (Branson 2510), ELISA reader (BioTek), mikropipet (Socorex), hemasitometer, lampu. Bahan yang digunakan dalam penelitian ini adalah ekstrak etanol daun kelengkeng, daun alpukat, dan daun kersen yang diperoleh dari ekstraksi serbuk daun menggunakan etanol 70%, akuades, culture flask, conical tube, kertas filter, media Roswell Park. Memorial Institute (RPMI), penisilinstreptomisin, fetal bovine serum (FBS), tripsin-EDTA, phosphate buffered saline (PBS), dimetil sulfoksida (DMSO), reagen. MTT (3-(4,5-dimetiltiazol-2-il)-2,5 difeniltetrazolium bromida), sodium dodesil sulfat (SDS) 10% dalam 0,01 N HCl, etanol. 70%, 96-well plate, microcentrifuge tube, sitroborat, FeCl3, anisaldehid-asam sulfat, nheksan p.a., aseton p.a., dan silika gel GF254

Uji Sitotoksik
HASIL DAN PEMBAHASAN Hasil uji sitotoksik ekstrak terhadap sel
Konsentrasi Sel WiDr
Daftar Pustaka
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