HPLC测定3种葛根素注射液中葛根素含量  

Determintion for Content of Puerarin in Three Kinds of Puerarin Injections by HPLC Method

作　　者：李昌勤[1] 李丹[1] 王培卿[1] 张丹[1] 康文艺[1] 程力[2] 

机构地区：[1]河南大学中药研究所,河南开封475004 [2]贵阳中医学院第二附属医院,贵阳550003

出　　处：《中国实验方剂学杂志》2014年第24期60-63,共4页Chinese Journal of Experimental Traditional Medical Formulae

基　　金：河南省科技厅重点攻关项目(122102310272);河南大学研究生教育综合改革项目(Y141108)

摘　　要：目的：应用高效液相色谱法同时测定葛根素注射液、葛根素葡萄糖注射液和葛根素氯化钠注射液中葛根素的含量。方法：采用Merk,Purospher STAR RP-C18色谱柱（4.6 mm×250 mm,5μm）,流动相甲醇-1%冰乙酸水溶液（25∶75）,流速1.0 m L·min^-1,柱温29℃,检测波长250 nm,进样量10μL。结果：对照品葛根素在0.192~1.152μg呈良好曲线关系,线性回归方程Y=468 374X＋3 105.25（r=0.999 8）,平均加样回收率为99.81%,RSD 0.42%。结论：3种注射液中的葛根素均可在选定的条件下得到较好的分离,线性关系良好。该方法简单快速、合理可行,可为葛根素注射液的质量控制提供科学依据。Objective： An HPLC method was established to determine the content of pueratin in three types of injection. Method： Separation was achieved by a Merk, Purospher STAR RP-C18 column used at 29 ~C , and mobile phase was methanol and 1% acetic acid, water with the flow rate of 1.0 mL·min^-1, detection wavelength of 250 nm. Result： The puerarin was separated with good linearity in the sample size range of 0. 192- 1. 152 μg. The average recovery was 99.81% , with RSD value of 0.42%. Conclusion： The puerarin in three types of puerarin injection could be well separated under the selected conditions, showing good linear relationship. The method was simple and quick, feasible and could provide scientific basis for the quality control of puerarin injection.

关 键 词：高效液相色谱法 葛根素注射液 葛根素葡萄糖注射液 葛根素氯化钠注射液 葛根素 

分 类 号：R284.1[医药卫生—中药学]