植物提取物对马拉塞菌药敏试验的研究

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摘要

以酮康唑为阳性参比标准物,对荷叶莲、木耳、鼠尾草、万寿菊、番石榴、银荷、木犀草、辣木、甘草等10种植物提取物的抑菌活性进行了研究。用不同浓度的提取物在不同溶剂中测定其抗疟菌效果。采用Kirby Bauer圆盘扩散法对10种植物提取物进行初步筛选,结果表明,金针叶水提物和金针叶乙醇提物对马拉色霉具有较强的抗真菌活性。采用薄层色谱(TLC)技术对菝葜和菝葜进行了分离纯化和部分鉴定。最小抑菌浓度(MIC)测定。以50 μg/ ml的酮康唑为对照品,Kirby - Bauer法对毛螨的药效分别为0.312mg/ ml和0.625mg/ ml。经植物化学分析,山茱萸和山茱萸均含有萜类、甾体、单宁和多酚类物质,其中多酚类物质和黄酮类物质含量显著高于山茱萸和山茱萸。因此,本研究得出结论,officinalis和H.sabdariffa对M. furfur具有有效的活性,从而减少头皮屑的流行,为未来的研究提供了前景,包括化合物的表征和细胞毒性。©2022 caproslaxy媒体。版权所有。
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An Indigenous Study on Malassezial Susceptibility Testing by Selected Plant Extracts
he present study was carried out to evaluate the antifungal activity of tenselected plant extracts of Nelumbo nucifera,Senna auriculata, Salvia officinalis, Tagetes erecta,Psidium guajava,Argemone mexicana,Hibiscussabdariffa, Hemidesmus indicus, Moringa oleifera,andGlycyrrhizaglabrawith ketoconazole as the positive reference standard. Their antimalassezial efficacy was tested using different concentrations of extracts in various solvents. The preliminary screening of plant extracts was determined by Kirby Bauer disc diffusion method and among the tenplantextracts, aqueous extract of S.officinalisand ethanol extract of H.sabdariffaextract exhibited potent antifungal activity against Malasseziafurfur. The purification and partial characterization of H. sabdariffa and S.officinalis were carriedout by Thin layer chromatography (TLC) technique.The Minimum Inhibitory Concentration (MIC) of H.sabdariffa andS.officinalisagainst M. furfur by Kirby Bauer method was0.312mg/mLand 0.625mg/mLrespectively against 50 μg/mLof Ketoconazole which was used as the standard. The phytochemical analysis of S.officinalis and H.sabdariffa revealed the presence of terpenoids, steroids, tannins, and polyphenols of which the concentration of polyphenols and flavonoids were significantly higher in S.officinalisand H.sabdariffa respectively. Thus, the present study concludes that S.officinalisand H.sabdariffa havea potent activity against M. furfur, thereby reducing the prevalence of dandruff, provided the future perspectives of the study that includecharacterization and cytotoxicity of the compound.©2022Caproslaxy Media. All rights reserved.
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