Antifungal activity and toxicity of bioactive compounds isolated from the leaf of Ximenia caffra Sond. var. natalensis

Q4 Economics, Econometrics and Finance Journal of Medicinal Plants for Economic Development Pub Date : 2023-12-19 DOI:10.4102/jomped.v7i1.219
D. M. Tlaamela, Salome Mahlo, M. Abdalla, L. McGaw
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Abstract

Background: Based on high frequency index, Ximenia caffra Sond. var. natalensis was selected for further phytochemical investigation and biological assays.Aim: The study aimed to isolate the active antifungal compounds from the leaves of X. caffra var. natalensis.Setting: The ethnobotanical study was conducted in Aganang Local Municipality, Capricorn District.Methods: Acetone extract was partitioned five times with hexane, chloroform, ethyl acetate, butanol and water, respectively. Fractions were screened for antifungal activity against Candida albicans using the microplate method and bioautography assays. The structures of isolated compounds were identified using nuclear magnetic resonance (NMR) and mass spectrometry. Cytotoxicity of isolated compounds was determined using 3-(4,5-dimethylthiazol)-2,5-diphenyl tetrazolium bromide (MTT) assay.Results: Bioassay-guided fractionation of the ethyl acetate fraction led to the isolation of four compounds, out of which only two were identified. Compound 1 was identified as epigallocatechin gallate, and Compound 3 was confirmed as kaempferol-3-O-rhamnoside. Epigallocatechin gallate exhibited moderate antifungal activity with minimum inhibitory concentration (MIC) of 0.5mg/mL and less toxic to the cells with LC50 = 32.32 µg/mL.Conclusion: The antifungal activity and cytotoxicity of isolated compounds validate the use of X. caffra Sond. var. natalensis in combating oral candidiasis.Contribution: The results have shown the potential bioactivity of X. caffra Sond. var. natalensis in the treatment of oral candidiasis.
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从 Ximenia caffra Sond. var. natalensis 叶中分离的生物活性化合物的抗真菌活性和毒性
研究背景目的:该研究旨在从 X. caffra var. natalensis 的叶子中分离出活性抗真菌化合物:人种植物学研究在摩羯区阿加南地方市进行:丙酮提取物分别与正己烷、氯仿、乙酸乙酯、丁醇和水进行五次分配。采用微孔板法和生物层析法筛选萃取物对白色念珠菌的抗真菌活性。利用核磁共振(NMR)和质谱鉴定了分离化合物的结构。利用 3-(4,5-二甲基噻唑)-2,5-二苯基溴化四唑(MTT)测定法确定了分离化合物的细胞毒性:在生物测定指导下对乙酸乙酯馏分进行分馏,分离出四种化合物,其中只有两种得到鉴定。化合物 1 被确认为表没食子儿茶素没食子酸酯,化合物 3 被确认为山奈酚-3-O-鼠李糖苷。表没食子儿茶素没食子酸酯表现出中等的抗真菌活性,最低抑菌浓度(MIC)为 0.5 毫克/毫升,对细胞的毒性较低,LC50 = 32.32 微克/毫升:结论:分离化合物的抗真菌活性和细胞毒性验证了 X. caffra Sond:结果表明,X. caffra Sond. var.
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来源期刊
Journal of Medicinal Plants for Economic Development
Journal of Medicinal Plants for Economic Development Economics, Econometrics and Finance-Economics and Econometrics
CiteScore
0.90
自引率
0.00%
发文量
14
审稿时长
32 weeks
期刊最新文献
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