褐藻分离次级代谢物对人念珠菌体外拮抗作用的研究。

A. Manilal, G. Ameya, T. Gezmu, B. Merdekios, S. Balu, AkbarIdhayadhulla, R. Kumar
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引用次数: 3

摘要

目的:考察褐藻的抗药力,并通过气相色谱-质谱分析阐明其生物活性原理。方法:对海洋褐藻S. swartzii进行有机溶剂提取和分离,定量分析其对5种临床相关念珠菌的体外抗念珠菌效力。结果:粗藻提取物的分离产生了生物活性的藻类部分,表现出最广泛的活性光谱。不同程度地抑制了酵母菌病原菌的生长。对白色念珠菌的最大活性记录。活性藻组分的气相色谱-质谱分析证实了三种化学成分的存在。因此,对人类念珠菌的有效广谱活性可能是由于主要原理1,2-苯二甲酸,二异辛酯的存在,或者可能与所有成分的协同活性有关。结论:本研究结果表明,该藻类部分的生物活性原理可作为先导分子开发天然抗真菌药物,以对抗致病性念珠菌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the In Vitro Antagonism of Secondary Metabolites Fractionated from the Brown Algae, Sargassum swartzii against Human Candida spp.
Objective: To inspect the anticandidal potency of brown algae S. swartzii and GC-MS analysis to delineate its bioactive principles. Methods: The marine brown algae S. swartzii, was extracted and fractionated in organic solvents and quantitatively analyzed for its in vitro anticandidal potency against a battery of five clinically relevant species of Candida. Results: The fractionation of the crude algal extract yielded a bioactive algal fraction that exhibited broadest spectra of activity. It impeded the growth of all the evaluated Yeast pathogens in variable degrees. The maximal activity was recorded against the Candida albicans. The GC-MS studies of active algal fraction evinced the presence of three chemical constituents. Thence, the potent broad spectra of activity against the human Candida could be due the presence of major principle 1,2-Benzenedicarboxylic acid, diisooctyl ester, or could be pertained to the synergistic activity all the components. Conclusion: The overall results of this study implicates that the bioactive principles found in this algal fraction could be utilized as a lead molecule to develop natural antifungal drug to combat pathogenic Candida species.
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