Cytotoxicity effects of Melastoma malabathricum leaves methanolic extract on cell viability / Wan Norshahadah Wan Shamsuddin

Melastoma malabathricum has a wide distribution around this part of the world. It has been reported to be found growing wild in Southeast Asia including Malaysia. The present study aims to determine the anticancer activities of methanolic extracts from the leaves of Melastoma malabathricum using var...

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Main Author: Wan Shamsuddin, Wan Norshahadah
Format: Thesis
Language:English
Published: 2012
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Online Access:https://ir.uitm.edu.my/id/eprint/66822/1/66822.pdf
https://ir.uitm.edu.my/id/eprint/66822/
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spelling my.uitm.ir.668222022-09-15T08:16:14Z https://ir.uitm.edu.my/id/eprint/66822/ Cytotoxicity effects of Melastoma malabathricum leaves methanolic extract on cell viability / Wan Norshahadah Wan Shamsuddin Wan Shamsuddin, Wan Norshahadah Botanical chemistry. Phytochemicals Cancer Herbs. Herbal teas Melastoma malabathricum has a wide distribution around this part of the world. It has been reported to be found growing wild in Southeast Asia including Malaysia. The present study aims to determine the anticancer activities of methanolic extracts from the leaves of Melastoma malabathricum using various established in vitro assays. Four types of cell lines were utilized in this study which were breast cancer cells (MCF-7), hepatocellular carcinoma cells (HepG2), colon cancer cells (HCT 116) and normal liver cells (WRL 68). Cells were plated in 96-well plates and incubated in conditions at 370C under 95% O2 and 5% CO2. Five concentrations of M. malabathricum extracts; 0.1 μg/ml, 1 μg/ml, 10 μg/ml, 100 μg/ml, 1000 μg/ml were selected to verify the anticancer activities and MTT assay was chosen as the method to measure the cell viability. Concentration response curve for methanol extract of M. malabathricum were constructed to determine the effects of concentration on cell viability and the median inhibitory concentration (IC50) was calculated for each cell line. IC50 for methanolic extract of M. malabathricum in MCF-7 cells, HepG2 cells, HCT 116 cells and WRL 68 cells were 126.9 ± 19.9μg/ml, 130.6 ± 29.3μg/ml, 124.9 ± 44.1μg/ml and 261.4 ± 17.7μg/ml respectively. . From the result, MCF-7, HepG2 and HCT 116 cells showed greater cytotoxic activity compared to WRL 68 cells as IC50, the concentration of the extract that provides 50% inhibition to the cells is lower compared to WRL 68. This study can contribute to the development of more effective, safer and cheaper natural based anticancer drugs. 2012 Thesis NonPeerReviewed text en https://ir.uitm.edu.my/id/eprint/66822/1/66822.pdf Cytotoxicity effects of Melastoma malabathricum leaves methanolic extract on cell viability / Wan Norshahadah Wan Shamsuddin. (2012) Degree thesis, thesis, Universiti Teknologi MARA (UiTM). <http://terminalib.uitm.edu.my/66822.pdf>
institution Universiti Teknologi Mara
building Tun Abdul Razak Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Mara
content_source UiTM Institutional Repository
url_provider http://ir.uitm.edu.my/
language English
topic Botanical chemistry. Phytochemicals
Cancer
Herbs. Herbal teas
spellingShingle Botanical chemistry. Phytochemicals
Cancer
Herbs. Herbal teas
Wan Shamsuddin, Wan Norshahadah
Cytotoxicity effects of Melastoma malabathricum leaves methanolic extract on cell viability / Wan Norshahadah Wan Shamsuddin
description Melastoma malabathricum has a wide distribution around this part of the world. It has been reported to be found growing wild in Southeast Asia including Malaysia. The present study aims to determine the anticancer activities of methanolic extracts from the leaves of Melastoma malabathricum using various established in vitro assays. Four types of cell lines were utilized in this study which were breast cancer cells (MCF-7), hepatocellular carcinoma cells (HepG2), colon cancer cells (HCT 116) and normal liver cells (WRL 68). Cells were plated in 96-well plates and incubated in conditions at 370C under 95% O2 and 5% CO2. Five concentrations of M. malabathricum extracts; 0.1 μg/ml, 1 μg/ml, 10 μg/ml, 100 μg/ml, 1000 μg/ml were selected to verify the anticancer activities and MTT assay was chosen as the method to measure the cell viability. Concentration response curve for methanol extract of M. malabathricum were constructed to determine the effects of concentration on cell viability and the median inhibitory concentration (IC50) was calculated for each cell line. IC50 for methanolic extract of M. malabathricum in MCF-7 cells, HepG2 cells, HCT 116 cells and WRL 68 cells were 126.9 ± 19.9μg/ml, 130.6 ± 29.3μg/ml, 124.9 ± 44.1μg/ml and 261.4 ± 17.7μg/ml respectively. . From the result, MCF-7, HepG2 and HCT 116 cells showed greater cytotoxic activity compared to WRL 68 cells as IC50, the concentration of the extract that provides 50% inhibition to the cells is lower compared to WRL 68. This study can contribute to the development of more effective, safer and cheaper natural based anticancer drugs.
format Thesis
author Wan Shamsuddin, Wan Norshahadah
author_facet Wan Shamsuddin, Wan Norshahadah
author_sort Wan Shamsuddin, Wan Norshahadah
title Cytotoxicity effects of Melastoma malabathricum leaves methanolic extract on cell viability / Wan Norshahadah Wan Shamsuddin
title_short Cytotoxicity effects of Melastoma malabathricum leaves methanolic extract on cell viability / Wan Norshahadah Wan Shamsuddin
title_full Cytotoxicity effects of Melastoma malabathricum leaves methanolic extract on cell viability / Wan Norshahadah Wan Shamsuddin
title_fullStr Cytotoxicity effects of Melastoma malabathricum leaves methanolic extract on cell viability / Wan Norshahadah Wan Shamsuddin
title_full_unstemmed Cytotoxicity effects of Melastoma malabathricum leaves methanolic extract on cell viability / Wan Norshahadah Wan Shamsuddin
title_sort cytotoxicity effects of melastoma malabathricum leaves methanolic extract on cell viability / wan norshahadah wan shamsuddin
publishDate 2012
url https://ir.uitm.edu.my/id/eprint/66822/1/66822.pdf
https://ir.uitm.edu.my/id/eprint/66822/
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score 13.160551