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中国精品科技期刊2020
郑亚美, 任娇艳, 史传超. 蜜柚叶黄酮的提取及其抗氧化与降尿酸活性研究[J]. 食品工业科技, 2017, (08): 262-266. DOI: 10.13386/j.issn1002-0306.2017.08.042
引用本文: 郑亚美, 任娇艳, 史传超. 蜜柚叶黄酮的提取及其抗氧化与降尿酸活性研究[J]. 食品工业科技, 2017, (08): 262-266. DOI: 10.13386/j.issn1002-0306.2017.08.042
ZHENG Ya-mei, REN Jiao-yan, SHI Chuan-chao. Extraction of flavonoids from Honey pomelo leaves and study on its antioxidant and uric acid reduction activities[J]. Science and Technology of Food Industry, 2017, (08): 262-266. DOI: 10.13386/j.issn1002-0306.2017.08.042
Citation: ZHENG Ya-mei, REN Jiao-yan, SHI Chuan-chao. Extraction of flavonoids from Honey pomelo leaves and study on its antioxidant and uric acid reduction activities[J]. Science and Technology of Food Industry, 2017, (08): 262-266. DOI: 10.13386/j.issn1002-0306.2017.08.042

蜜柚叶黄酮的提取及其抗氧化与降尿酸活性研究

Extraction of flavonoids from Honey pomelo leaves and study on its antioxidant and uric acid reduction activities

  • 摘要: 研究蜜柚叶总黄酮的提取工艺、抗氧化活性及其对黄嘌呤氧化酶的抑制活性。采用正交实验对蜜柚叶黄酮的提取工艺进行优化,探究蜜柚叶黄酮的最佳提取工艺条件。并通过DPPH自由基、羟自由基及超氧阴离子清除实验探究蜜柚叶黄酮对自由基离子的清除活性;通过黄嘌呤氧化酶活性抑制实验初步判断其降尿酸功效。结果表明:蜜柚叶黄酮的最佳提取条件为料液比1:30(g/mL)、乙醇浓度80%、浸提时间6 h、浸提温度80℃,黄酮得率为12.41 mg/g。蜜柚叶黄酮对DPPH自由基、羟自由基及超氧阴离子均表现出较强的清除活性,IC50值分别为:1.47、1.04、1.49 mg/mL。同时,蜜柚叶黄酮对黄嘌呤氧化酶抑制活性的IC50值为4.8 mg/mL。 

     

    Abstract: In order to investigate the extraction processes of flavonoids from Honey pomelo leaves and its antioxidant and uric acid reduction activities, the extraction conditions of flavonoids were optimized primarily by orthogonal array design.In addition, the DPPH·, hydroxyl free radical and superoxide anion free radical scavenging activities were determined to evaluate the antioxidant activity of the flavonoids and the inhibition of xanthine oxidase activity was determined to preliminary judging its uric acid reduction activity.Results indicated that optimal extraction processing parameters were the ratio of material to solvent of 1: 30 ( g/mL) , ethanol concentration of 80%, extraction temperature of 80 ℃, extraction time of 6 h, the extraction efficiency of flavonoids from Honey pomelo leaves was 12.41 mg/g. Meanwhile, in DPPH radical, hydroxyl radical and superoxide anion scavenging assays, the IC50 of the scavenging activities of flavonoids from Honey pomelo leaves were 1.47, 1.04 mg/mL and1.49 mg/mL. The inhibition of xanthine oxidase assay illustrated that the flavonoids showed a certain degree of suppression effect of xanthine oxidase ( IC50: 4.8 mg/mL) .

     

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