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对萼猕猴桃叶中黄酮类成分的含量分析
引用本文:吴迎春,辛海量,盛佳钰,张亚妮,凌昌全.对萼猕猴桃叶中黄酮类成分的含量分析[J].中医药学刊,2010(5):954-958.
作者姓名:吴迎春  辛海量  盛佳钰  张亚妮  凌昌全
作者单位:[1]上海中医药大学中药化学教研室,上海201203 [2]第二军医大学长海医院,上海200433
基金项目:国家自然科学基金资助项目(30572360); 上海市科委中药现代化专项基金资助项目(04DZ19808)
摘    要:目的:分析对萼猕猴桃叶中总黄酮以及黄酮类成分山柰酚-3-O-β-D-吡喃半乳糖苷(ry-1)、对萼猕猴桃苷E(ry-2)、对萼猕猴桃苷F(ry-3)的含量,为对萼猕猴桃叶品质评价和质量控制提供依据。方法:采用芦丁比色法对对萼猕猴桃叶中总黄酮进行含量分析;建立HPLC法对对萼猕猴桃叶中黄酮类成分ry-1、ry-2、ry-3进行含量分析。色谱柱:Shim-packCLC-ODS色谱柱(4.6mm×25mm,5μm);保护柱:DIKMAEasy-Guard C18(10mm×4.6mm),流动相:乙腈-0.5%醋酸水溶液梯度洗脱;柱温:26℃;检测波长:360nm;流速:1.00mL/min。结果:总黄酮的回归方程为A=8.26×10^-2+1.90×10^-3,r=0.9995,线性范围:0.01~0.09mg/mL;ry-1回归方程为A=6.84×10^-5C+6.53×10^-2,r=0.9999,线性范围:0.792~23.760μg/mL;ry-2回归方程为A=8.58×10^-5C+0.124,r=0.9999,线性范围:2.570~77.100μg/mL;ry-3回归方程为A=7.89×10^-5C+9.54×10-2,r=0.9999,线性范围:2.168~65.040μg/mL。结论:该方法前处理简便,分析准确、快速,可以作为对萼猕猴桃叶中总黄酮以及ry-1、ry-2、ry-3的定量分析方法,也为对萼猕猴桃叶的质量控制和品质评价提供了重要的依据。

关 键 词:对萼猕猴桃叶  黄酮  含量测定  HPLC

Quantitative Analysis of Flavonoids in Leaves of Actinidia valvata
WU Ying-chun,XIN Hai-liang,SHENG Jia-yu,ZHANG Ya-ni,LING Chang-Quan.Quantitative Analysis of Flavonoids in Leaves of Actinidia valvata[J].Study Journal of Traditional Chinese Medicine,2010(5):954-958.
Authors:WU Ying-chun  XIN Hai-liang  SHENG Jia-yu  ZHANG Ya-ni  LING Chang-Quan
Affiliation:1.Department of Traditional Chinese Medicine Chemistry,Shanghai University of Traditional Chinese Medicine,Shanghai 201203,China;2.Changhai Hospital of Second Military Medical University,Shanghai 200433,China)
Abstract:Objective:To determine content of total flavonoid and in leaves of Actinidia valvata,which may provide experimental evidence for its qualitative control and evaluation.Methods:Rutoside-UV method was used for the determination of total flavonoid and HPLC method was developed for the determination of kaempferol-3-O-β-D-galactopyranoside(ry-1),actinoside E(ry-2) and actinoside F(ry-3) in leaves of Actinidia valvata.The HPLC method was developed with the conditions as following:Shim-pack CLC-ODS column(4.6mm×25mm,5μm),DIKMA Easyguard C18 (10mm×4.6mm),gradient elution was employed with the mobile phase acetonitrile-0.5% acetic acid solution at flow rate of 1.00mL/min;Column temperature:26 ℃;Detection wavelength:360 nm.Results:The standard curves of total flavonoid,ry-1,ry-2 and ry-3 were A=8.26×10^-2C+ 1.90×10^-3 (r=0.9995),A=6.84×10^-5C +6.53×10^-2 (r=0.9999),A=8.58×10^-5C+0.124(r=0.9999) and A=7.89×10^-5C +9.54×10^-2 (r=0.9999),respectively.The standard curves of total ry-1,ry-2 and ry-3 were linear in the range of 0.01~0.09 mg/mL,0.792~23.760 μg/mL,2.570~77.100μg/mL and 2.168~65.040μg/mL,respectively.Conclusion:The method is feasible for quantitative analysis of total flavonoid,ry-1,ry-2 and ry-3 in leaves of Actinidia valvata,and also provided meaningful evidence for its qualitative control and evaluation.
Keywords:leaves of Actinidia valvata  flavonoid  quantitative-analysis  HPLC
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