...
首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Development of a novel ion-pairing UPLC method with cation-exchange solid-phase extraction for determination of free timolol in human plasma
【24h】

Development of a novel ion-pairing UPLC method with cation-exchange solid-phase extraction for determination of free timolol in human plasma

机译:一种具有阳离子交换固相萃取的新型离子配对UPLC方法,用于测定人血浆中游离薯醇的方法

获取原文
获取原文并翻译 | 示例
           

摘要

A novel UPLC-UV method was developed for analysis of timolol in human plasma using a simple, fast, and cost effective ion-exchange SPE procedure, followed by separation on a C-18 UPLC column with a mobile phase consisting of acetonitrile, phosphate buffer, and sodium 1-octane sulfonate as an ion pairing agent. The method was fully validated according to US-FDA guidelines, and was found to be sufficiently accurate and precise for analysis of timolol in human plasma for clinical pharmacokinetic studies. The application of ion-exchange SPE cartridges for purification of timolol in plasma produced excellent percent recoveries and good sample clean-up, while the ion-pairing separation described here allowed quantitation of timolol without interference from endogenous sample components. The method lower limit of detection was 1.7 ng/mL and the lower limit of quantitation was 5.0 ng/mL, allowing for analysis of therapeutic concentrations of timolol in plasma.
机译:开发了一种新型UPLC-UV方法,用于使用简单,快速,经济高效的离子交换SPE程序分析人血浆中的氏炎,然后在C-18 UPLC柱上分离,其流动相由乙腈,磷酸盐缓冲液组成 ,和1-辛烷磺酸钠作为离子配对剂。 该方法根据US-FDA指南完全验证,发现对临床药代动力学研究的人血浆中氏酒醇进行了足够的准确和精确。 离子交换SPE盒在血浆中纯化纯化的纯化产生优异的回收率和良好的样品清理,而这里描述的离子配对分离允许定量氏炎,而不会从内源样品组分干扰干扰。 检测的方法下限为1.7 ng / ml,定量下限为5.0ng / ml,允许分析血浆中蒂罗酚的治疗浓度。

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