HPLC法测定隔山消中没食子酸的含量研究  

Determination of Gallic Acid in Geranium Strictipe R. Kunth by HPLC

作　　者：肖培云[1] 蓝海[1] 李龙星[1] 

机构地区：[1]大理学院药学院,云南大理671000

出　　处：《大理学院学报（综合版）》2009年第6期9-11,共3页Journal of Dali University

基　　金：云南省教育厅科研基金资助项目(08C0194);大理州科学技术局资助项目(08DL102)

摘　　要：目的:建立HPLC法测定隔山消中没食子酸的含量。方法:测定没食子酸的色谱条件是Agilent ZOR-BAX SB C18色谱柱(4.6mm×150mm,5μm),流动相为甲醇-0.4%磷酸水溶液(10∶90),检测波长为273nm,流速为1.0ml/min,柱温为25℃。结果:没食子酸在0.05～0.5μg范围内线性关系良好,r值为0.999 9,平均回收率为98.46%,RSD为2.56%。结论:本法操作简便、快速、分离效果好、稳定性高、重现性好,为建立隔山消质量标准和进一步研究隔山消提供科学依据。Objective： To establish a method for determination of gallic acid in Geranium strictipe R.Kunth. Method： The chromatographic condition for gallic acid was that the Agilent ZORBAX SB C18 （4.6mm×150mm,5μm） was used; the mobile phase consisted of CH3OH-H2O （0.4%H3PO4）; the UV wavelength of gallic acid was 273nm; the flow rate was 1.0ml/min; the temperature of column was 25℃. Result： Gallic acid was good linearity over the range of 0.05-0.5μg,（r=0.999 9）, The average recovery was 98.46%; RSD was 2.56%. Conclusion： The method is simple, sensitive, accurate, reproducible and can be used to control the quality of Geranium strictipes R.Kunth.

关 键 词：隔山消 没食子酸 高效液相色谱 

分 类 号：R917[医药卫生—药物分析学]