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高效液相色谱法测定生物样品中萘哌地尔浓度

METHODOLOGICAL STUDY ON THE DETERMINATILN OF NAFTOPIDIL CONCENTRATION IN BIOLOGICAL SAMPLES BY HPLC

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【作者】 於东晖万里涛楼雅卿

【Author】 DH Yu,LT Wan and YQ Lou(Department of Pharmacology,Bijing Medical Universty,Beijing100083)

【机构】 北京医科大学基础医学院药理学系

【摘要】 以美托洛尔为内标,建立了HPLC-UV测定大鼠血浆、尿、粪、胆汁及肝脑组织匀浆中药物浓度的方法。流动相为甲醇、乙腈、水及0.2mol·L-1醋酸钠缓冲液,以C18柱分离,紫外检测波长232nm,生物样品在不同条件下经两次乙醚处理可获得良好分离。血浆样品最低检测浓度为5ng·ml-1,日内RSD和日间RSD为3.17~10.88%,平均回收率为79.35~95.72%。本法简便、灵敏、可靠,经大鼠单次灌胃20mg·kg-1后血药浓度的测定验证,可满足临床前药代动力学研究的需要。

【Abstract】 A method was developed for the determination of the novel antihypertensive drugnaftopidil in biological samples by HPLC,Metoprolol was used as the internal standard.The analyticalcolumn was a stainless steel column filled with 10 μmC1s packing.The mobile phase was a mixture ofmethanol-acetonitrile-water-0.2 mol·L-1Ac-0.2 mol·L-1aAc(50 :45 :5:0.9:0.1).Detection was performed at UV 232 nm,Biologieal samples can be well purified after twoextractions with ether.The lowest detection limit was 5 ng· ml-1.The precision and accuracywithin-day and day-to-day ranged from 3.17 to l0. 88%,The mean recoveries were 79.35%to95.72%,The results showed that this method was simple,sensitive and good enough to be used inpharmacokinetic study of naftopidil。

【关键词】 高效液相色谱法萘哌地尔药代动力学
【Key words】 HPLCNaftopidilPharmacokinetics
  • 【文献出处】 药学学报 ,ACTA PHARMACEUTICA SINICA , 编辑部邮箱 ,1995年04期
  • 【分类号】R927.2
  • 【被引频次】10
  • 【下载频次】77
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