首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Validation of a LC-fluorescence method for determination of free captopril in human plasma, using a pre-column derivatization reaction with monobromobimane.
【24h】

Validation of a LC-fluorescence method for determination of free captopril in human plasma, using a pre-column derivatization reaction with monobromobimane.

机译:液相色谱荧光法测定人血浆中游离卡托普利的有效性,该方法采用了柱前衍生化反应与一溴二苯胺。

获取原文
获取原文并翻译 | 示例

摘要

Both derivatization of free captopril in human plasma samples using monobromobimane as fluorescent label and the corresponding HPLC-fluorescence detection (FLD) method were validated. Calibration curve for the fluorescent captopril derivative in plasma samples is linear in the ppb-ppm range with a detection limit of 4 ppb and an identification limit of 10 ppb (P%: 90; nu>/=5). These methods were successfully applied on bioequivalence studies carried out on some marketed pharmaceutical formulations.
机译:验证了使用单溴二苯醚作为荧光标记衍生化人血浆样品中游离卡托普利的方法和相应的HPLC-荧光检测(FLD)方法。血浆样品中荧光卡托普利衍生物的校准曲线在ppb-ppm范围内呈线性,检测限为4 ppb,鉴定限为10 ppb(P%:90; nu> = 5)。这些方法已成功应用于对某些市售药物制剂进行的生物等效性研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号