Lanckmans Katrien, Sarre Sophie, Smolders Ilse, Michotte Yvette
Research Group Experimental Pharmacology, Department of Pharmaceutical Chemistry, Drug Analysis and Drug Information, Vrije Universiteit Brussel, Laarbeeklaan 103, 1090 Brussels, Belgium.
Talanta. 2008 Jan 15;74(4):458-69. doi: 10.1016/j.talanta.2007.07.027. Epub 2007 Aug 2.
Microdialysis (MD) is an in vivo sampling technique used to investigate biochemical events in the extracellular fluid of animal and human tissues. MD produces protein- and cell-free, aqueous samples which can be analyzed without further sample clean-up. Liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) is a sensitive and selective analysis technique which is suitable to quantify low concentrated target analytes in microdialysates. This paper reviews the LC-MS/MS methods which are described for the quantification of endogenous molecules, such as neurotransmitters and peptides, and of exogenous molecules, such as drugs, in microdialysates. Since miniaturization of the LC-MS/MS methods is the key to obtain maximal sensitivity of the analytical technique, this feature is discussed in the paper. In addition, critical issues related to the quantification of low concentrated molecules in microdialysates are described such as the presence of matrix effects, the low MD efficiency and the sticking of, for instance, neuropeptides.
微透析(MD)是一种体内采样技术,用于研究动物和人体组织细胞外液中的生化事件。微透析产生无蛋白质和细胞的水性样品,无需进一步样品净化即可进行分析。液相色谱-串联质谱联用(LC-MS/MS)是一种灵敏且具有选择性的分析技术,适用于定量微透析液中低浓度的目标分析物。本文综述了用于定量微透析液中内源性分子(如神经递质和肽)以及外源性分子(如药物)的LC-MS/MS方法。由于LC-MS/MS方法的小型化是获得该分析技术最大灵敏度的关键,本文对此特性进行了讨论。此外,还描述了与微透析液中低浓度分子定量相关的关键问题,如基质效应的存在、微透析效率低以及例如神经肽的黏附等。