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快速 MALDI-MS 法在生物基质药物定量分析中的应用:经验教训、新进展和未来展望。

Rapid MALDI-MS Assays for Drug Quantification in Biological Matrices: Lessons Learned, New Developments, and Future Perspectives.

机构信息

Department of Clinical Pharmacology and Pharmacoepidemiology, Heidelberg University Hospital, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.

National Center for Tumor Diseases Heidelberg, Department of Medical Oncology, Heidelberg University Hospital, Im Neuenheimer Feld 460, 69120 Heidelberg, Germany.

出版信息

Molecules. 2021 Feb 26;26(5):1281. doi: 10.3390/molecules26051281.

DOI:10.3390/molecules26051281
PMID:33652935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7956427/
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.

摘要

基质辅助激光解吸/电离质谱(MALDI-MS)在治疗药物监测领域的应用很少,部分原因是待定量化合物与多种 MALDI 基质之间的电离过程复杂。开发符合监管指南中关于生物分析方法验证的可行 MALDI-MS 方法需要事先了解以下方面的适用性:(i) MALDI 基质与分析物类别和电离特性,(ii) MALDI 基质的结晶特性与自动化功能,以及 (iii) 用于实现灵敏和特异测量的 MS 仪器,以便在生物基质中测定低药理学药物浓度。在本综述文章/白皮书,我们回顾了建立 MALDI-MS 测定法以定量组织和血浆中药物所需的发展,并用具体结果说明了不同步骤。我们总结了根据监管机构的要求,成功开发完全验证的 MALDI-MS 方法所需的必要参数,以及目前尚未解决的问题和有希望解决这些问题的方法。最后,我们提出了关于未来展望和需求的专家意见,以确立 MALDI-MS 作为治疗药物监测的通用方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78dd/7956427/b3e58ef9343c/molecules-26-01281-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78dd/7956427/fe640f0fb639/molecules-26-01281-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78dd/7956427/3a8f0f1e7c15/molecules-26-01281-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78dd/7956427/ae90af797a73/molecules-26-01281-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78dd/7956427/9da26fbf942e/molecules-26-01281-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78dd/7956427/b3e58ef9343c/molecules-26-01281-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78dd/7956427/fe640f0fb639/molecules-26-01281-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78dd/7956427/3a8f0f1e7c15/molecules-26-01281-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78dd/7956427/ae90af797a73/molecules-26-01281-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78dd/7956427/9da26fbf942e/molecules-26-01281-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78dd/7956427/b3e58ef9343c/molecules-26-01281-g005.jpg

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