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In vitro anti-cancer efficacy and phyto-chemical screening of solvent extracts of Kigelia africana (Lam.) Benth

BACKGROUND AND OBJECTIVES: Kigelia africana is a medicinal plant growing naturally in many parts of Africa. In Kenya, a water concoction of the plant is used to treat breast and prostate cancers. Laboratory data on its anti-cancer activity and active principles is limited, hence no scientific ration...

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Autores principales: Wambua Mukavi, Justus, Wafula Mayeku, Philip, Muhoro Nyaga, Justin, Naulikha Kituyi, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372144/
https://www.ncbi.nlm.nih.gov/pubmed/32715139
http://dx.doi.org/10.1016/j.heliyon.2020.e04481
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author Wambua Mukavi, Justus
Wafula Mayeku, Philip
Muhoro Nyaga, Justin
Naulikha Kituyi, Sarah
author_facet Wambua Mukavi, Justus
Wafula Mayeku, Philip
Muhoro Nyaga, Justin
Naulikha Kituyi, Sarah
author_sort Wambua Mukavi, Justus
collection PubMed
description BACKGROUND AND OBJECTIVES: Kigelia africana is a medicinal plant growing naturally in many parts of Africa. In Kenya, a water concoction of the plant is used to treat breast and prostate cancers. Laboratory data on its anti-cancer activity and active principles is limited, hence no scientific rationale for its medicinal use. This study reports on in-vitro toxic activities of dichloromethane and methanol extracts of the plant against human breast cancer cells and phytochemical screening of the two extracts. METHODOLOGY: Plant extracts were obtained by sequential solvent extraction of dry plant material (stem bark) using analytical grade dichloromethane: methanol (1:1) and methanol (Sigma Aldrich). In-vitro anti-cancer activities of the extracts were determined using the suphorhodamine (SRB) assay against a human breast cancer cell line (HCC 1937). Preliminary Thin layer chromatography of plant extracts was done using POLYGRAM® SIL G/UV(254) plates (Merck) to establish presence of different classes of secondary metabolites. RESULTS: In-vitro cytotoxic activities of the two extracts were significantly different (P = 0.05). The methanol extract exhibited higher activity (IC(50) = 26.02 μg/ml) compared to that of dichloromethane: methanol (1:1) (IC(50) = 55.01 μg/ml). Phyto-chemical screening of the two extracts revealed the presence of terpenoids, phenols, steroids and flavonoids. CONCLUSION: The high in-vitro anti-cancer activities of solvent extracts of Kigelia africana justify its use in traditional medicine to manage breast cancer. Phytochemical analysis of the extracts reveal similar profiles hence the differences in their anti-cancer activities can be attributed to quantitative variations of various classes of secondary metabolites.
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spelling pubmed-73721442020-07-23 In vitro anti-cancer efficacy and phyto-chemical screening of solvent extracts of Kigelia africana (Lam.) Benth Wambua Mukavi, Justus Wafula Mayeku, Philip Muhoro Nyaga, Justin Naulikha Kituyi, Sarah Heliyon Article BACKGROUND AND OBJECTIVES: Kigelia africana is a medicinal plant growing naturally in many parts of Africa. In Kenya, a water concoction of the plant is used to treat breast and prostate cancers. Laboratory data on its anti-cancer activity and active principles is limited, hence no scientific rationale for its medicinal use. This study reports on in-vitro toxic activities of dichloromethane and methanol extracts of the plant against human breast cancer cells and phytochemical screening of the two extracts. METHODOLOGY: Plant extracts were obtained by sequential solvent extraction of dry plant material (stem bark) using analytical grade dichloromethane: methanol (1:1) and methanol (Sigma Aldrich). In-vitro anti-cancer activities of the extracts were determined using the suphorhodamine (SRB) assay against a human breast cancer cell line (HCC 1937). Preliminary Thin layer chromatography of plant extracts was done using POLYGRAM® SIL G/UV(254) plates (Merck) to establish presence of different classes of secondary metabolites. RESULTS: In-vitro cytotoxic activities of the two extracts were significantly different (P = 0.05). The methanol extract exhibited higher activity (IC(50) = 26.02 μg/ml) compared to that of dichloromethane: methanol (1:1) (IC(50) = 55.01 μg/ml). Phyto-chemical screening of the two extracts revealed the presence of terpenoids, phenols, steroids and flavonoids. CONCLUSION: The high in-vitro anti-cancer activities of solvent extracts of Kigelia africana justify its use in traditional medicine to manage breast cancer. Phytochemical analysis of the extracts reveal similar profiles hence the differences in their anti-cancer activities can be attributed to quantitative variations of various classes of secondary metabolites. Elsevier 2020-07-19 /pmc/articles/PMC7372144/ /pubmed/32715139 http://dx.doi.org/10.1016/j.heliyon.2020.e04481 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Wambua Mukavi, Justus
Wafula Mayeku, Philip
Muhoro Nyaga, Justin
Naulikha Kituyi, Sarah
In vitro anti-cancer efficacy and phyto-chemical screening of solvent extracts of Kigelia africana (Lam.) Benth
title In vitro anti-cancer efficacy and phyto-chemical screening of solvent extracts of Kigelia africana (Lam.) Benth
title_full In vitro anti-cancer efficacy and phyto-chemical screening of solvent extracts of Kigelia africana (Lam.) Benth
title_fullStr In vitro anti-cancer efficacy and phyto-chemical screening of solvent extracts of Kigelia africana (Lam.) Benth
title_full_unstemmed In vitro anti-cancer efficacy and phyto-chemical screening of solvent extracts of Kigelia africana (Lam.) Benth
title_short In vitro anti-cancer efficacy and phyto-chemical screening of solvent extracts of Kigelia africana (Lam.) Benth
title_sort in vitro anti-cancer efficacy and phyto-chemical screening of solvent extracts of kigelia africana (lam.) benth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7372144/
https://www.ncbi.nlm.nih.gov/pubmed/32715139
http://dx.doi.org/10.1016/j.heliyon.2020.e04481
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