| Literature DB >> 33652935 |
Margaux Fresnais1, Esra Yildirim1, Seda Karabulut1, Dirk Jäger2, Inka Zörnig2, Julia Benzel3,4, Kristian W Pajtler3,4,5, Stefan M Pfister3,4,5, Jürgen Burhenne1, Walter E Haefeli1, Rémi Longuespée1.
Abstract
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) has rarely been used in the field of therapeutic drug monitoring, partly because of the complexity of the ionization processes between the compounds to be quantified and the many MALDI matrices available. The development of a viable MALDI-MS method that meets regulatory guidelines for bioanalytical method validation requires prior knowledge of the suitability of (i) the MALDI matrix with the analyte class and properties for ionization, (ii) the crystallization properties of the MALDI matrix with automation features, and (iii) the MS instrumentation used to achieve sensitive and specific measurements in order to determine low pharmacological drug concentrations in biological matrices. In the present hybrid article/white paper, we review the developments required for the establishment of MALDI-MS assays for the quantification of drugs in tissues and plasma, illustrated with concrete results for the different steps. We summarize the necessary parameters that need to be controlled for the successful development of fully validated MALDI-MS methods according to regulatory authorities, as well as currently unsolved problems and promising ways to address them. Finally, we propose an expert opinion on future perspectives and needs in order to establish MALDI-MS as a universal method for therapeutic drug monitoring.Entities:
Keywords: MALDI; mass spectrometry; targeted quantification; therapeutic drug monitoring
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Year: 2021 PMID: 33652935 PMCID: PMC7956427 DOI: 10.3390/molecules26051281
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411