首页 | 本学科首页   官方微博 | 高级检索  
检索        

高效液相色谱法测定抗骨增生丸中淫羊藿苷的含量
引用本文:蒋桂平.高效液相色谱法测定抗骨增生丸中淫羊藿苷的含量[J].中南药学,2008,6(3):322-323.
作者姓名:蒋桂平
作者单位:湖南省涟钢医院,湖南,娄底,417009
摘    要:目的建立抗骨增生丸中淫羊藿苷含量的高效液相色谱法测定方法。方法样品经处理后,由Diamonsil C18(4.6mm×200mm,5μm)色谱柱分离,流动相:乙腈-水(26∶74),流速:1.0mL.min^-1,检测波长:270nm。结果方法分离良好,样品中杂质不干扰淫羊藿苷的分离测定,淫羊藿苷浓度在0.0404-0.504μg内与峰面积线性关系好,r=0.9999,平均回收率为98.4%,RSD为0.7%(n=6)。结论本法测定简便,结果准确,重复性和分离度好,可用于抗骨增生丸的质量控制。

关 键 词:高效液相色谱法  淫羊藿苷  抗骨增生丸  含量测定
文章编号:1672-2981(2008)04-0322-02
修稿时间:2008年3月6日

Determination of icariin in kangguzengsheng pills by HPLC
JIANG Gui-ping.Determination of icariin in kangguzengsheng pills by HPLC[J].Central South Pharmacy,2008,6(3):322-323.
Authors:JIANG Gui-ping
Institution:JIANG Gui-ping(Liangang Hospital of Hunan Province,Loudi Hunan 417009)
Abstract:Objective To develop an HPLC method for the determination of icariin in Kangguzengsheng pills.Methods A C18 column(4.6 mm×200 mm,5 μm),and a mobile phase composed of acetonitrile-water(26∶74)were adopted.The flow rate was 1.0 mL·min^-1 and wave length was 270 nm.Results The linear range was 0.040 4~0.504 μg,r=0.999 98.The recovery of paeoniflorin was 98.4% with RSD=0.7%(n=6).Conclusion The determination method is simple and accurate,and can be used for the quality control of Kangguzengsheng pills.
Keywords:HPLC  icariin  kangguzengsheng pills  determination
本文献已被 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号