Unit Toxicology, National Institute of Criminalistics and Criminology (NICC), Brussels, Belgium.
Department of Toxicology, Laboratoire de Sciences Judiciaires et de Médecine Légale, 1701 Parthenais St., Montréal, Québec, H2K 3S7, Canada.
Curr Pharm Des. 2022;28(15):1230-1244. doi: 10.2174/1381612828666220526152259.
The use of high-resolution mass spectrometry (HRMS) has increased over the past decade in clinical and forensic toxicology, especially for comprehensive screening approaches. Despite this, few guidelines in this field have specifically addressed HRMS issues concerning compound identification, validation, measurement uncertainty and quality assurance. To fully implement this technique, certainly in an era in which the quality demands for laboratories are ever-increasing due to various norms (e.g. the International Organization for Standardization's ISO 17025), these specific issues need to be addressed. This manuscript reviews 26 HRMSbased methods for qualitative systematic toxicological analysis (STA) published between 2011 and 2021. Key analytical data such as samples matrices, analytical platforms, numbers of analytes and employed mass spectral reference databases/libraries as well as the studied validation parameters are summarized and discussed. The article further includes a critical review of targeted and untargeted data acquisition approaches, available HRMS reference databases and libraries as well as current guidelines for HRMS data interpretation with a particular focus on identification criteria. Moreover, it provides an overview on current recommendations for the validation and determination of measurement uncertainty of qualitative methods. Finally, the article aims to put forward suggestions for method development, compound identification, validation experiments to be performed, and adequate determination of measurement uncertainty for this type of wide-range qualitative HRMSbased methods.
过去十年,高分辨率质谱(HRMS)在临床和法医毒理学中的应用有所增加,尤其是在全面筛选方法中。尽管如此,该领域几乎没有专门针对化合物鉴定、验证、测量不确定度和质量保证的 HRMS 问题的指南。为了充分实施这项技术,特别是在由于各种规范(例如国际标准化组织的 ISO 17025)对实验室的质量要求不断提高的时代,需要解决这些具体问题。本文回顾了 2011 年至 2021 年间发表的 26 种基于 HRMS 的定性系统毒理学分析(STA)方法。总结和讨论了关键分析数据,如样品基质、分析平台、分析物数量以及所采用的质谱参考数据库/库以及研究的验证参数。文章进一步对靶向和非靶向数据采集方法、可用的 HRMS 参考数据库和库以及 HRMS 数据解释的当前指南进行了批判性审查,特别侧重于鉴定标准。此外,它还概述了目前针对定性 HRMS 方法的验证和测量不确定度确定的建议。最后,本文旨在为这类广泛的定性 HRMS 方法的方法开发、化合物鉴定、验证实验的开展以及测量不确定度的充分确定提出建议。