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人血浆中缬沙坦的药物浓度
引用本文:刘红梅,刘艳,金锐,王珍,孙考祥,陆义诚.高效液相色谱法测定人血浆中缬沙坦的药物浓度[J].中国药房,2001,12(7):414-415.
作者姓名:刘红梅  刘艳  金锐  王珍  孙考祥  陆义诚
作者单位:哈尔滨医科大学附属二院药学部
摘    要:目的 :测定人血浆中缬沙坦的药物浓度。方法 :采用液固萃取法提取 ,高效液相色谱法测定。色谱柱 :HypersilODSC18(4 6nm×200nm ,5μm ) ;流动相 :乙腈 -0 01mol/L的磷酸盐缓冲液 (50∶50 ,pH2 8) ;流速 :1 5ml/min ;荧光检测器 :λex为265nm ,λem为378nm。结果 :缬沙坦的保留时间为5 4min ,定量线性范围0 05~5μg/ml,方法回收率>90 % (n=5) ,日内、日间RSD<10 % (n=5)。结论 :本法快速 ,定量准确 ,可用于血药浓度测定及人体药代动力学研究

关 键 词:缬沙坦  血药浓度  高效液相色谱法
文章编号:1001-0408(2001)07-0414-02
修稿时间:2001年1月17日

Determination of Valsartan Concentration in Human Plasma With HPLC
LIU Hongmei,LIU Yan,JIN Rui,WANG Zhen,SUN Kaoxiang,LU Yicheng.Determination of Valsartan Concentration in Human Plasma With HPLC[J].China Pharmacy,2001,12(7):414-415.
Authors:LIU Hongmei  LIU Yan  JIN Rui  WANG Zhen  SUN Kaoxiang  LU Yicheng
Abstract:OBJECTIVE:To determine the valsartan concentration in human plasma METHODS:The plasma sample was extracted with a liquid-solid method and determined with HPLC,stationary phase was Hypensil ODS C18(4 6nm×200nm,5μm),mobile phase consisted of acetonitrile and 0 01mol/L KH2PO4 buffer(pH 2 8)(50∶50) The flow rate was 1 5ml/min Detection was performed with fluorescence detector at λex 265nm,λem 378nm RESULTS:The retention time of valsartan was about 5 4 minutes,and the linear range of quantity was 0 05~5μg/ml The recoveries of methodology were more than 90%(n=5) Inter-day and intra-day RSD were less then 10%(n=5) CONCLUSION:This method is rapid and accurate It can be applied to determining the plasma valsartan concentration and studying on pharmacokinetics
Keywords:valsartan  plasma concentration of drug  HPLC  
本文献已被 CNKI 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