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液相色谱-串联质谱定量蛋白质组学在药物代谢与转运的体外-体内外推中的转化价值及选择合适技术的考量

Translational value of liquid chromatography coupled with tandem mass spectrometry-based quantitative proteomics for in vitro-in vivo extrapolation of drug metabolism and transport and considerations in selecting appropriate techniques.

作者信息

Al Feteisi Hajar, Achour Brahim, Rostami-Hodjegan Amin, Barber Jill

机构信息

a 1 Manchester Pharmacy School, University of Manchester , Oxford Road, Manchester, M13 9PT, UK.

出版信息

Expert Opin Drug Metab Toxicol. 2015;11(9):1357-69. doi: 10.1517/17425255.2015.1055245. Epub 2015 Jun 26.

Abstract

INTRODUCTION

Drug-metabolizing enzymes and transporters play an important role in drug absorption, distribution, metabolism and excretion and, consequently, they influence drug efficacy and toxicity. Quantification of drug-metabolizing enzymes and transporters in various tissues is therefore essential for comprehensive elucidation of drug absorption, distribution, metabolism and excretion. Recent advances in liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) have improved the quantification of pharmacologically relevant proteins.

AREAS COVERED

This report presents an overview of mass spectrometry-based methods currently used for the quantification of drug-metabolizing enzymes and drug transporters, mainly focusing on applications and cost associated with various quantitative strategies based on stable isotope-labeled standards (absolute quantification peptide standards, quantification concatemers, protein standards for absolute quantification) and label-free analysis.

EXPERT OPINION

In mass spectrometry, there is no simple relationship between signal intensity and analyte concentration. Proteomic strategies are therefore complex and several factors need to be considered when selecting the most appropriate method for an intended application, including the number of proteins and samples. Quantitative strategies require appropriate mass spectrometry platforms, yet choice is often limited by the availability of appropriate instrumentation. Quantitative proteomics research requires specialist practical skills and there is a pressing need to dedicate more effort and investment to training personnel in this area. Large-scale multicenter collaborations are also needed to standardize quantitative strategies in order to improve physiologically based pharmacokinetic models.

摘要

引言

药物代谢酶和转运体在药物吸收、分布、代谢和排泄过程中发挥着重要作用,因此会影响药物疗效和毒性。所以,对各种组织中的药物代谢酶和转运体进行定量分析,对于全面阐明药物吸收、分布、代谢和排泄至关重要。液相色谱-串联质谱联用技术(LC-MS/MS)的最新进展提高了药理学相关蛋白质的定量分析能力。

涵盖领域

本报告概述了目前用于定量分析药物代谢酶和药物转运体的基于质谱的方法,主要关注基于稳定同位素标记标准品(绝对定量肽标准品、定量串联体、绝对定量蛋白质标准品)和无标记分析的各种定量策略的应用及成本。

专家观点

在质谱分析中,信号强度与分析物浓度之间不存在简单的关系。因此,蛋白质组学策略较为复杂,在为特定应用选择最合适的方法时需要考虑多个因素,包括蛋白质数量和样本数量。定量策略需要合适的质谱平台,但选择往往受到合适仪器可用性的限制。定量蛋白质组学研究需要专业的实践技能,迫切需要投入更多精力和资源来培训该领域的人员。还需要开展大规模多中心合作,以规范定量策略,从而改进基于生理的药代动力学模型。

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