北阿坎德邦加尔瓦尔地区抗氧化成分的地理变异:中国制动蕨(Pteris vittata)

K. Dobhal, A. Semwal, A. Negi
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引用次数: 2

摘要

生物体内存在多种抗氧化剂或保护剂,如谷胱甘肽是肝脏产生的主要抗氧化剂,利用自由基净化身体。天然植物中抗氧化剂的含量越来越受到科学研究和工业应用的关注。蕨类植物(蕨类和蕨类同属植物)自古以来就受到植物探索者和园艺界的关注。在北阿坎德邦不同的地理区域采集了维塔翼属植物。以乙醇为溶剂提取的植物提取物得率最高,为5.07 ~ 9.67%。DPPH自由基清除试验表明,DPPH提取物在0.1 mg/ml浓度下对抗坏血酸的抑制率最高为89.32%,接近91.96%。结果表明,DPV提取物和抗坏血酸的IC50分别为0.543和0.495 mg/ml。过氧化氢自由基清除率为0.8 mg/ml时,DPV提取物对BHA的最大抑制率为72.33%,相对接近77.42%。结果表明,DPV提取物和BHA的IC50值分别为0.279±0.005 mg/ml和0.257±0.002 mg/ml。DPV提取物对抗坏血酸的最大抑制率为84.32%,接近于0.8 mg/ml的抗坏血酸的抑制率87.96%。DPV提取物和BHA的IC50值为0.233±0.002 mg/ml ~ 0.218±0.006 mg/ml。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Geographical Variation of Antioxidant Constituent in Garhwal Region of Uttarakhand: Chinese Brake Fern (Pteris vittata)
Numerous kind of antioxidants or protecting agent are present in the living body like Glutathione is the master antioxidant produce by the liver and uses free radicals to purify the body. Natural plant consuming antioxidants content is growing the interest for scientific research as well as industrial purposes. Pteridophytes (fern and fern allies) have drawn attention of plants seekers and horticultures since ancient period. Plant of Pteris vittata were collected from different geographical region of Uttarakhand Garhwal. The maximum yield of plant extract was found via the ethanol solvent i.e. 5.07-9.67%. DPV extract exhibited a maximum inhibition of 89.32 relatively closed to 91.96% inhibition of Ascorbic acid at the concentration of 0.1 mg/ml by DPPH radical scavenging assay method. The IC50 of the DPV extract and Ascorbic acid was found to be 0.543 and 0.495 mg/ml by same. DPV extract showed a maximum inhibition of 72.33 % relatively close to 77.42% inhibition of BHA at the concentration of 0.8 mg/ml by Hydrogen peroxide radical scavenging method. The IC50 value of the DPV extract & BHA was found to be 0.279 ± 0.005 mg/ml & 0.257 ± 0.002 mg/ml by same. DPV extract showed a maximum inhibition of 84.32% relatively close to 87.96% inhibition of ascorbic acid at the concentration of 0.8 mg/ml by Nitrogen oxide scavenging method. The IC50 value of the DPV extract & BHA was found to be 0.233 ± 0.002 mg/ml to 0.218 ± 0.006 mg/ml by same.
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