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HPLC法测定云南青牛胆清除DPPH自由基活性能力 被引量:5

DPPH radical scavenging activity of the extract from Tinospora sagittata var.yunnanensis
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摘要 采用HPLC法研究了不同溶剂对云南青牛胆提取物清除1,1-二苯基-2-三硝基苯肼(DPPH)自由基测定的方法。实验结果表明,云南青牛胆提取物具有良好的自由基清除能力,其顺序为:乙醇〉乙酸乙酯〉正丁醇〉丙酮。其中,乙醇提取物(IC50为0.69 mg/m L)的清除能力最大,除丙酮提取物(IC50为1.93 mg/m L)外,其他提取物的自由基清除能力均大于香草酸(IC50为1.82 mg/m L)的清除能力;相关分析结果表明,各提取物在一定浓度范围内与自由基清除率呈现良好的线性关系,DPPH自由基浓度c在0.1-1.0 mg/m L的浓度范围内与峰面积A呈线性相关,A=11146c-1083.3,r=0.9991。 DPPH(1,1-pheny-2-picrylhydrazyl) radical scavenging activities of the extracts of Tinospora sagittata var.yunnanensis in different solvent were analyzed by HPLC methods.The experimental results showd that the extracts have a good ability of DPPH radical scavenging activities,and the order is ethanolethyl acetaten-buohacetone.Among them,the ethanol extract(IC50 was 0.69 mg/mL) removal capacity is the largest,in addition to the acetone extracts(IC50 was 1.93 mg/mL),the DPPH radical scavenging capacity of other extract is greater than the vanillic acid(IC50 was 1.82 mg/mL).There are good linear relationships between the extracts in the certain concentration range and scavenging free radicals.Similarly,the mass concentration of DPPH radical in the range of 0.1 -1.0 mg/mL and the peak area also has a good linear relationship,the regression equation and the correlation coefficient is A=11146C-1083.3and 0.9991,respectively.
出处 《食品科技》 CAS 北大核心 2015年第7期314-317,共4页 Food Science and Technology
基金 国家自然科学基金项目(51262031 51462036) 云南省绿色化学与功能材料研究创新团队项目(2011HC008) 云南省高校绿色化学新能源与材料科技创新团队项目(2011UYN09)
关键词 云南青牛胆 DPPH自由基 HPLC 抗氧化活性 Tinospora sagittata var.yunnanensis DPPH radical HPLC antioxidative activity
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