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自动化固相微萃取和薄膜微萃取在高通量生物流体分析和配体-受体结合研究中的应用。

Automated solid-phase microextraction and thin-film microextraction for high-throughput analysis of biological fluids and ligand-receptor binding studies.

机构信息

Department of Chemistry, University of Waterloo, Waterloo, Ontario, Canada.

出版信息

Nat Protoc. 2010 Jan;5(1):140-61. doi: 10.1038/nprot.2009.180. Epub 2010 Jan 7.

Abstract

This protocol describes how to perform automated solid-phase microextraction (SPME) and thin-film microextraction (TFME) in a 96-well plate format for high-throughput analysis of drugs, metabolites and any other analytes of interest in biological fluids using liquid chromatography-electrospray tandem mass spectrometry. Sample preparation time required is typically 1 min per sample; hence, the throughput achievable with automated SPME/TFME is comparable with automated 96-well liquid-liquid extraction and solid-phase extraction methods, but greater than most online solid-phase extraction methods. The technique is applicable to complex samples such as whole blood without additional pretreatment. The amount of analyte extracted by SPME/TFME is proportional to the free (unbound) concentration of the analyte; hence, SPME/TFME can be used to determine both total and free concentrations of analytes from a single biofluid sample and to perform automated ligand-receptor binding studies in order to determine binding affinity and/or overall extent of ligand binding to a complex biofluid.

摘要

本方案描述了如何在 96 孔板格式中进行自动化固相微萃取(SPME)和薄膜微萃取(TFME),以使用液相色谱-电喷雾串联质谱法对生物体液中的药物、代谢物和任何其他感兴趣的分析物进行高通量分析。通常,每个样品的样品制备时间需要 1 分钟;因此,自动化 SPME/TFME 的通量可与自动化 96 孔液-液萃取和固相萃取方法相媲美,但大于大多数在线固相萃取方法。该技术适用于全血等复杂样品,无需额外预处理。SPME/TFME 萃取的分析物量与分析物的游离(未结合)浓度成正比;因此,SPME/TFME 可用于从单个生物流体样品中同时测定分析物的总浓度和游离浓度,并进行自动化配体-受体结合研究,以确定配体与复杂生物流体的结合亲和力和/或结合程度。

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