金合欢乙酸乙酯部位多酚类化合物的抗氧化活性研究。

Q1 Chemistry Chemistry Central Journal Pub Date : 2018-01-25 DOI:10.1186/s13065-018-0373-x
Tayyaba Afsar, Suhail Razak, Maria Shabbir, Muhammad Rashid Khan
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引用次数: 43

摘要

背景:水合金合欢属豆科植物,具有抗氧化、抗炎和抗癌活性。在我们的研究过程中,我们进行了生物测定引导分离,得到了具有自由基清除活性的抗氧化化合物。材料与方法:采用真空液相色谱和中压液相色谱相结合的方法,对水草提取物中的多酚类化合物进行分离。采用高压液相色谱、质谱esi和核磁共振等方法对分离化合物的结构非均质性进行了表征。采用1,1-二苯基-2-吡啶酰肼(DPPH)、一氧化氮清除电位、羟基自由基清除电位、铁还原/抗氧化能力(FRAP)模型体系和总抗氧化能力测定等方法研究了分离化合物的抗氧化能力。结果:分离得到的化合物具有7- o -没食子酸儿茶素、儿茶素和没食子酸甲酯的显性信号。快速色谱分离得到750毫克的7-O没食子酸儿茶素,400毫克的儿茶素和150毫克的没食子酸甲酯从4克装载的部分ISCO。结果表明,C1对DPPH (EC50为1.60±0.035µM)、一氧化氮自由基(EC50为6±0.346µM)的抗氧化能力最强,12.5µM剂量下的抗氧化指数(1.710±0.04)和FRAP(649.5±1.5µM Fe(II)/g)的抗氧化能力最强,C3对OH自由基的清除能力较C2、C3低(4.33±0.618µM)。结论:首次报道了水仙多酚类化合物的抗氧化活性。结果表明,该方法简便、准确,与提取液中其他成分分离效果好。新种中儿茶素的分离为从绿茶中获得大量儿茶素和儿茶素异构体提供了多种途径。从水杨中分离的儿茶素异构体的自由基清除特性值得进一步研究这种植物在氧化应激相关疾病中的消耗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Antioxidant activity of polyphenolic compounds isolated from ethyl-acetate fraction of Acacia hydaspica R. Parker.

Background: Acacia hydaspica belongs to family leguminosae possess antioxidant, anti-inflammatory and anticancer activities. During our search for antioxidant compounds from A. hydaspica, we carried out bioassay guided fractionation and obtained antioxidant compounds with free radical scavenging activity.

Materials and methods: The polyphenol compounds in the plant extract of A. hydaspica were isolated by combination of different chromatographic techniques involving vacuum liquid chromatography and medium pressure liquid chromatography. The structural heterogeneity of isolated compounds was characterized by high pressure liquid chromatography, MS-ESI and NMR spectroscopic analyses. The antioxidant potential of isolated compounds has been investigated by 1,1-diphenyl-2-picrylhydrazyl (DPPH), nitric oxide scavenging potential, hydroxyl radical scavenging potential, ferric reducing/antioxidant power (FRAP) model systems and total antioxidant capacity measurement.

Results: The isolated compounds show the predominance of signals representative of 7-O-galloyl catechins, catechins and methyl gallate. Flash chromatographic separation gives 750 mg of 7-O galloyl catechin, 400 mg of catechin and 150 mg of methyl gallate from 4 g loaded fraction on ISCO. Results revealed that C1 was the most potent compound against DPPH (EC50 1.60 ± 0.035 µM), nitric oxide radical (EC50 6 ± 0.346 µM), showed highest antioxidant index (1.710 ± 0.04) and FRAP [649.5 ± 1.5 µM Fe(II)/g] potency at 12.5 µM dose compared to C2, C3 and standard reference, whereas C3 showed lower EC50 values (4.33 ± 0.618 µM) in OH radical scavenging assay.

Conclusion: Present research reports for the first time the antioxidant activity of polyphenolic compounds of A. hydaspica. Result showed good resolution and separation from other constituents of extract and method was found to be simple and precise. The isolation of catechin from this new species could provide a varied opportunity to obtain large quantities of catechin and catechin isomers beside from green tea. Free radical scavenging properties of isolated catechin isomers from A. hydaspica merit further investigations for consumption of this plant in oxidative stress related disorders.

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来源期刊
Chemistry Central Journal
Chemistry Central Journal 化学-化学综合
CiteScore
4.40
自引率
0.00%
发文量
0
审稿时长
3.5 months
期刊介绍: BMC Chemistry is an open access, peer reviewed journal that considers all articles in the broad field of chemistry, including research on fundamental concepts, new developments and the application of chemical sciences to broad range of research fields, industry, and other disciplines. It provides an inclusive platform for the dissemination and discussion of chemistry to aid the advancement of all areas of research. Sections: -Analytical Chemistry -Organic Chemistry -Environmental and Energy Chemistry -Agricultural and Food Chemistry -Inorganic Chemistry -Medicinal Chemistry -Physical Chemistry -Materials and Macromolecular Chemistry -Green and Sustainable Chemistry
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