茴香不同提取物抗氧化活性的比较。种子

Fatema Tuz Zohera, R. Habib, M. Z. Imam, Ehsanul Hoque Mazumder, S. Rana
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引用次数: 11

摘要

摘要本研究旨在比较芹菜种子甲醇、乙酸乙酯、pet醚和水提取物的抗氧化能力。采用总酚和类黄酮含量测定法、总抗氧化能力、1,1-二苯基-2-苦酰肼(DPPH)自由基测定法、还原能力测定法、一氧化氮(NO)清除法和铜离子还原能力测定法(CUPRAC法)评价抗氧化活性。提取物表现出中等的抗氧化活性,且呈剂量依赖性。提取物中含有酚类化合物和类黄酮化合物。在DPPH自由基清除实验中,乙酸乙酯提取物的ic50值较抗坏血酸最低,为585.58μg/ml。在一氧化氮清除实验中,水、甲醇、乙酸乙酯和Pet醚提取物的ic50值分别为122.99μg/ml、320.54μg/ml、601.81μg/ml和206.37μg/ml,而参比抗坏血酸的ic50值为6.83μg/ml。提取物也表现出良好的还原力。本研究结果表明,该提取物具有显著的抗氧化潜力,其中乙酸乙酯提取物具有最高的抗氧化潜力。关键词:蛇芹;抗氧化剂;DPPH;没有清除;CUPRAC;ROS。DOI: 10.3329/sjps.v3i1.6802 S. J. Pharm。科学通报3(1):68-74
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Antioxidant Potential of Different Extracts of Celastrus paniculatus Willd. Seed
The objective of the present study was to evaluate the comparative antioxidant potential of methanol, ethyl acetate, pet ether and water extracts of Celastrus paniculatus seed. Antioxidant activity was evaluated by using total phenol and flavonoid content determination assays, total antioxidant capacity, 1,1-diphenyl-2- picryl-hydrazil (DPPH) free radical assay, Reducing power assessment, Nitric oxide (NO) scavenging assay and Cupric ion reducing capacity assay (CUPRAC method). The extracts showed moderate antioxidant activity in a dose dependent manner. The extracts were found to contain phenolics and flavonoid compounds. In DPPH radical scavenging assay, ethyl acetate extract had the lowest IC 50 value (585.58μg/ml) compared to ascorbic acid. In nitric oxide scavenging assay IC 50 value was found to be 122.99μg/ml, 320.54μg/ml, 601.81μg/ml and 206.37μg/ml respectively for the Water, Methanol, Ethyl Acetate and Pet Ether extracts compared to 6.83μg/ml which was the IC 50 value for the reference ascorbic acid. The extracts also showed good reducing power. The results of the present study indicate that the extracts possesses significant antioxidant potential of which ethyl acetate extract is the most promising one and possess highest antioxidant potential. Key Words: Celastrus paniculatus ; antioxidant; DPPH; NO scavenging; CUPRAC; ROS. DOI: 10.3329/sjps.v3i1.6802 S. J. Pharm. Sci. 3(1): 68-74
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