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通过比较流动-流动电膜萃取-质谱系统与液相色谱-质谱联用仪获得的药物代谢谱验证电膜萃取的实时萃取动力学

Real Time Extraction Kinetics of Electro Membrane Extraction Verified by Comparing Drug Metabolism Profiles Obtained from a Flow-Flow Electro Membrane Extraction-Mass Spectrometry System with LC-MS.

作者信息

Fuchs David, Jensen Henrik, Pedersen-Bjergaard Stig, Gabel-Jensen Charlotte, Hansen Steen Honoré, Petersen Nickolaj Jacob

机构信息

Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen, Denmark.

出版信息

Anal Chem. 2015 Jun 2;87(11):5774-81. doi: 10.1021/acs.analchem.5b00981. Epub 2015 May 11.

DOI:10.1021/acs.analchem.5b00981
PMID:25920035
Abstract

A simple to construct and operate, "dip-in" electromembrane extraction (EME) probe directly coupled to electrospray ionization-mass spectrometry (ESI-MS) for rapid extraction and real time analysis of various analytes was developed. The setup demonstrated that EME-MS can be used as a viable alternative to conventional protein precipitation followed by liquid chromatography-mass spectrometry (LC-MS) for studying drug metabolism. Comparison of EME-MS with LC-MS for drug metabolism analysis demonstrated for the first time that real time extraction of analytes by EME is possible. Metabolism kinetics were investigated for three different drugs: amitriptyline, promethazine, and methadone. By comparing the EME-MS extraction profiles of the drug substances and formed drug metabolites with the metabolism profiles obtained by conventional protein precipitation followed by LC-MS good correlation was obtained with only very limited time delay in the extraction. The results indicate that, by tuning the electromembrane properties, for example, by optimizing the extraction voltage, extremely fast extraction kinetics can be obtained. A metabolic profile could be generated while the drug was metabolized offering a significant time saving as compared to conventional LC-MS where laborious protein precipitation or other sample pretreatments are required before analysis. This makes the developed EME-MS setup a highly promising sample preparation method for various kinds of applications where fast and real-time analysis of analytes is of interest.

摘要

开发了一种易于构建和操作的“浸入式”电膜萃取(EME)探针,该探针直接与电喷雾电离质谱(ESI-MS)耦合,用于快速萃取和实时分析各种分析物。该装置表明,对于研究药物代谢,EME-MS可作为传统蛋白质沉淀后接液相色谱-质谱(LC-MS)的可行替代方法。EME-MS与LC-MS在药物代谢分析方面的比较首次表明,通过EME实时萃取分析物是可行的。研究了三种不同药物(阿米替林、异丙嗪和美沙酮)的代谢动力学。通过将药物物质和形成的药物代谢物的EME-MS萃取图谱与传统蛋白质沉淀后接LC-MS获得的代谢图谱进行比较,在萃取过程中仅存在非常有限的时间延迟的情况下,获得了良好的相关性。结果表明,通过调整电膜特性,例如通过优化萃取电压,可以获得极快的萃取动力学。在药物代谢时可以生成代谢图谱,与传统的LC-MS相比,这节省了大量时间,传统LC-MS在分析前需要进行费力的蛋白质沉淀或其他样品预处理。这使得所开发的EME-MS装置成为一种极具前景的样品制备方法,适用于各种需要对分析物进行快速和实时分析的应用。

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