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In vitro antioxidant and cytotoxicity activities of selected indigenous South African medicinal plants

BACKGROUND: Medicinal plants are regarded as a large source of phytochemicals that may have anticancer properties. This could lead to the development of innovative drugs or alternative therapy against cancer. OBJECTIVE: This study was designed to determine the antioxidant and cytotoxicity effect of...

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Autores principales: Vakele, Yonela, Odun-Ayo, Frederick, Reddy, Lalini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Makerere Medical School 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9382541/
https://www.ncbi.nlm.nih.gov/pubmed/36032452
http://dx.doi.org/10.4314/ahs.v22i1.48
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author Vakele, Yonela
Odun-Ayo, Frederick
Reddy, Lalini
author_facet Vakele, Yonela
Odun-Ayo, Frederick
Reddy, Lalini
author_sort Vakele, Yonela
collection PubMed
description BACKGROUND: Medicinal plants are regarded as a large source of phytochemicals that may have anticancer properties. This could lead to the development of innovative drugs or alternative therapy against cancer. OBJECTIVE: This study was designed to determine the antioxidant and cytotoxicity effect of 5 selected indigenous South African medicinal plants namely; Bulbine frutescens, Bulbine natalensis, Chlorophytum comosum, Kniphofia uvaria, and Tulbaghia violacea. METHOD: Phytochemical extracts namely; methanol, 50%, 100% ethanol, and water extracts were prepared from the root and shoot of the plants. The antioxidant effect of methanol extracts of the plant materials was performed using a DPPH assay. A preliminary cytotoxicity screening of the phytochemical extracts in the human colon (Caco-2), cervical (HeLa), and hepatocellular (HepG2) cell lines were determined followed by the half-maximal inhibitory concentration (IC50) using MTT assay. RESULT: The methanol root extract of B. natalensis and B. frutescens (33.20% and 26.33% respectively) and shoot extract of K. uvaria (17.10%) showed the highest antioxidant. Out of the 5 plants, only 100% ethanol extract of C. comosum, K. uvaria, and T. violacea caused more than 80% cytotoxicity in HepG2 and Caco-2 cell lines. The shoot of B. frutescens (10.43 µg/ml), K. uvaria (23.0 µg/ml), and root of C. comosum (23.77 µg/ml) were the most active with the highest cytotoxicity. CONCLUSION: C. comosum, K. uvaria, and T. violacea possess significant cytotoxicity that is promising in developing alternative drugs against colon and liver cancers. Our results provided new pieces of evidence for antioxidant and cytotoxic activities of these plants which could be useful for developing new anticancer therapies.
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spelling pubmed-93825412022-08-25 In vitro antioxidant and cytotoxicity activities of selected indigenous South African medicinal plants Vakele, Yonela Odun-Ayo, Frederick Reddy, Lalini Afr Health Sci Articles BACKGROUND: Medicinal plants are regarded as a large source of phytochemicals that may have anticancer properties. This could lead to the development of innovative drugs or alternative therapy against cancer. OBJECTIVE: This study was designed to determine the antioxidant and cytotoxicity effect of 5 selected indigenous South African medicinal plants namely; Bulbine frutescens, Bulbine natalensis, Chlorophytum comosum, Kniphofia uvaria, and Tulbaghia violacea. METHOD: Phytochemical extracts namely; methanol, 50%, 100% ethanol, and water extracts were prepared from the root and shoot of the plants. The antioxidant effect of methanol extracts of the plant materials was performed using a DPPH assay. A preliminary cytotoxicity screening of the phytochemical extracts in the human colon (Caco-2), cervical (HeLa), and hepatocellular (HepG2) cell lines were determined followed by the half-maximal inhibitory concentration (IC50) using MTT assay. RESULT: The methanol root extract of B. natalensis and B. frutescens (33.20% and 26.33% respectively) and shoot extract of K. uvaria (17.10%) showed the highest antioxidant. Out of the 5 plants, only 100% ethanol extract of C. comosum, K. uvaria, and T. violacea caused more than 80% cytotoxicity in HepG2 and Caco-2 cell lines. The shoot of B. frutescens (10.43 µg/ml), K. uvaria (23.0 µg/ml), and root of C. comosum (23.77 µg/ml) were the most active with the highest cytotoxicity. CONCLUSION: C. comosum, K. uvaria, and T. violacea possess significant cytotoxicity that is promising in developing alternative drugs against colon and liver cancers. Our results provided new pieces of evidence for antioxidant and cytotoxic activities of these plants which could be useful for developing new anticancer therapies. Makerere Medical School 2022-03 /pmc/articles/PMC9382541/ /pubmed/36032452 http://dx.doi.org/10.4314/ahs.v22i1.48 Text en © 2022 Vakele Y et al. https://creativecommons.org/licenses/by/4.0/Licensee African Health Sciences. This is an Open Access article distributed under the terms of the Creative commons Attribution License (https://creativecommons.org/licenses/BY/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Vakele, Yonela
Odun-Ayo, Frederick
Reddy, Lalini
In vitro antioxidant and cytotoxicity activities of selected indigenous South African medicinal plants
title In vitro antioxidant and cytotoxicity activities of selected indigenous South African medicinal plants
title_full In vitro antioxidant and cytotoxicity activities of selected indigenous South African medicinal plants
title_fullStr In vitro antioxidant and cytotoxicity activities of selected indigenous South African medicinal plants
title_full_unstemmed In vitro antioxidant and cytotoxicity activities of selected indigenous South African medicinal plants
title_short In vitro antioxidant and cytotoxicity activities of selected indigenous South African medicinal plants
title_sort in vitro antioxidant and cytotoxicity activities of selected indigenous south african medicinal plants
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9382541/
https://www.ncbi.nlm.nih.gov/pubmed/36032452
http://dx.doi.org/10.4314/ahs.v22i1.48
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