Institute of Clinical Pharmacology, Medical Faculty Carl Gustav Carus, Dresden University of Technology, 01307 Dresden, Germany.
Leibniz Institute of Polymer Research Dresden and the Max Bergmann Center of Biomaterials, 01069 Dresden, Germany.
J Chromatogr A. 2018 Feb 2;1535:80-87. doi: 10.1016/j.chroma.2018.01.001. Epub 2018 Jan 2.
Liquid chromatography with electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) technique is gaining more and more attraction as the method of choice for multi-sample analysis. However, it is strongly susceptible to the influence of matrix components. Matrix effects are the main source of substantial losses in detection sensitivity and have to be compensated via complex quantification methods In this work, we introduce a sophisticated quantification method for the LC-ESI-MS/MS analysis of 16 substances in urine samples using a single continuously post-column infused internal standard (PCI-IS) for matrix effect correction. The performance of the introduced technique was proven by the simultaneous quantification using internal standards. Our results demonstrate that a single post-column infused internal standard suffices to analyze multiple target analytes. The introduced method is a new approach to analyze complex matrices and represents a powerful alternative to the classic internal standard methodology. The proposed technique significantly reduces the required steps for sample preparation, costs of additional stable isotopically-labeled internal standards, and self-induced matrix effects.
液相色谱-电喷雾串联质谱(LC-ESI-MS/MS)技术作为多样品分析的首选方法,越来越受到关注。然而,它非常容易受到基质成分的影响。基质效应是检测灵敏度大幅损失的主要原因,必须通过复杂的定量方法进行补偿。在这项工作中,我们引入了一种复杂的定量方法,用于使用单个连续柱后注入内标(PCI-IS)进行基质效应校正的尿液样品中 16 种物质的 LC-ESI-MS/MS 分析。同时使用内标进行定量证明了所介绍技术的性能。我们的结果表明,单个柱后注入的内标足以分析多个目标分析物。所介绍的方法是分析复杂基质的新方法,是经典内标方法的有力替代方法。该技术大大减少了样品制备所需的步骤、额外稳定同位素标记内标物的成本以及自诱导的基质效应。