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Column-switching procedures for the fast analysis of drugs in biologic samples.

机译:快速切换生物样品中药物的色谱柱切换程序。

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摘要

Liquid chromatography coupled with mass spectrometry in single and dual mode (LC-MS and LC-MS/MS) is the method of choice for the quantification of drugs and their metabolites in biologic fluids. Following the new challenges encountered in the process of drug development, liquid chromatography-mass spectrometry has been found to achieve high-throughput analysis. With this impressive tool, the sample preparation step before analysis is simplified, and the analytic process speeded up. Several generic approaches have recently been developed for the sample extraction coupled on line with a LC-MS system. In this paper, different extraction supports allowing the direct injection of biologic fluids were investigated, namely, restricted-access media, large-size particle, and monolithic phases. In the column-switching configuration, these supports, coupled with microbore analytic columns, were found suitable for the fast analysis (total analysis time of less than 10 minutes) of different drugs and their metabolites in biologic matrices at the nanogram per milliliter level.
机译:液相色谱与单模式和双模式质谱联用(LC-MS和LC-MS / MS)是定量生物流体中药物及其代谢物的一种选择方法。继药物开发过程中遇到的新挑战之后,发现液相色谱-质谱联用技术可实现高通量分析。有了这个令人印象深刻的工具,可以简化分析之前的样品制备步骤,并加快分析过程。最近开发了几种通用方法,用于与LC-MS系统在线耦合的样品提取。在本文中,研究了允许直接注入生物流体的不同萃取载体,即限制进入的介质,大粒径颗粒和整体相。在柱切换配置中,发现这些支持物与微孔分析柱相结合,适用于在生物基质中以纳克/毫升为水平快速分析不同药物及其代谢产物的总分析时间(少于10分钟)。

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