DPPH法测定白花檵木乙醇提取物及其不同极性部位抗氧化活性  

Determination of the Antioxidant Activity of Ethanol Extract and Its Different Polarity Fractions from Loropetalum chinense with DPPH Assay in vitro

作　　者：邵海华[1] 何明珍[2] 张武岗[1,2] 欧阳辉[1] 冯育林[1,2] 杨世林[1,2] 

机构地区：[1]江西中医学院,江西南昌330006 [2]中药固体制剂制造技术国家工程研究中心,江西南昌330006

出　　处：《时珍国医国药》2013年第7期1577-1579,共3页Lishizhen Medicine and Materia Medica Research

基　　金：国家"十一五"科技支撑计划重点项目(No.2009BADC3B03);江西省博士后科研项目择优资助项目(No.2012);江西省卫生厅中医药科研计划项目(No.2012A162)

摘　　要：目的研究白花檵木乙醇提取物及其不同极性部位体外抗氧化活性。方法对白花檵木乙醇提取物及其经大孔树脂分离所得洗脱物,进行DPPH自由基清除实验;并通过紫外吸收光谱扫描分析其化学组成。结果白花檵木乙醇提取物及各极性部位均具有较强抗氧化活性且呈浓度依赖性。其中乙醇提取物的IC50值为(17.54±0.71)μg/ml,10%乙醇洗脱物的IC50值为(11.47±0.91)μg/ml,70%乙醇洗脱物的IC50值为(9.73±0.26)μg/ml。结论白花檵木乙醇提取物具有较强抗氧化活性,经大孔树脂纯化,抗氧化能力显著增强。Objective To investigate the in vitro antioxidant activity of ethanol extract and its different polarities from Loropetalum chinense.Methods The DPPH radical scavenging activity was investigated by dividing an ethanol extract of Loropetalum chinense into four fractions from macroporous resin.Absorption spectrums of active parts were scanned from 190 to 900nm.Results The extract and its different polarities exhibited significant and dose-dependent DPPH free radical scavenging activities.The 50% inhibitory concentration（IC50） values were（17.54 ± 0.71） μg / ml for the extract,（11.47 ± 0.91） μg / ml for 10% ethanol eluate and（9.73 ± 0.26） μg / ml for 70% ethanol eluate.Conclusion 10% and 70% ethanol eluates from Macroporous resin exhibited significant antioxidant activity comparable to this obtained from the extract of Loropetalum chinense.

关 键 词：白花檵木 DPPH 鞣质 黄酮 抗氧化活性 

分 类 号：R285[医药卫生—中药学]