A broad-spectrum LC-MS/MS method for screening and quantification of 100 analytes in clinical and autopsy blood samples

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of Chromatography B Pub Date : 2024-09-18 DOI:10.1016/j.jchromb.2024.124323
Dimitra Florou , Mathew Di Rago , Amvrosios Orfanidis , Dimitri Gerostamoulos , Vassiliki A. Boumba
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Abstract

Liquid chromatography coupled with mass spectrometry (LC-MS) has been tremendously used for screening purposes in forensic toxicology, because of their great adaptability and reasonable time/resource consumption. Herein, a fully validated method based on liquid-liquid extraction (LLE) in human whole blood, by a multiple reaction monitoring (MRM) analysis through LC-MS/MS, is described. The proposed method simultaneously detects 100 analytes (plus three deuterated internal standard compounds) belonging to many different classes, including drugs of abuse, prescription and over-the-counter drugs commonly involved in poisoning and medical malpractice cases in our territory, as well as certain new psychoactive substances (NPS) and toxic substances potentially associated with adverse effects. The optimised LLE employs one extraction step of 200 μL blood using 0.1 M HCl methyl-tert-butyl-ether (MTBE) (acidified with concentrated HCl) proved to be suitable for the extraction of basic and neutral substances; as a reconstitution solvent a mixture of 88:12v/v, 0.1 % formic acid in 10 mM aqueous ammonium acetate, pH 3.5: 0.1 % formic acid in acetonitrile was used, yielding satisfactory recoveries for all analytes. The method was sensitive, showing low LOD/ LOQ for all substances ranging from 0.01 to 5/ 0.05–20 ng/mL, respectively. Linearity ranged between 0.05–500 ng/mL (R2 = 0.9811–0.9995), and the inter- and intra-day precisions ranged between 3–15 % and 7–18 %, respectively. Accuracy was evaluated in terms of percentage recovery, lying within acceptable range. The matrix effect expressed as ion suppression/enhancement of each analyte was in the range ±25 % for all analytes. Post-preparative stability of analytes was higher than 85 %, while no carryover between runs was observed. The developed method has been successfully applied in routine toxicological analyses for the analysis of biological samples from clinical and autopsy cases.

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用于筛查和量化临床及尸检血液样本中 100 种分析物的广谱 LC-MS/MS 方法
液相色谱-质谱联用技术(LC-MS)因其极高的适应性和合理的时间/资源消耗,在法医毒理学筛选中得到了广泛应用。本文介绍了一种基于液液萃取(LLE)、通过 LC-MS/MS 进行多反应监测(MRM)分析的人体全血检测方法。该方法可同时检测 100 种不同类别的分析物(外加三种氚代内标化合物),其中包括滥用药物、我国中毒和医疗事故案例中常见的处方药和非处方药,以及某些新精神活性物质(NPS)和可能产生不良影响的有毒物质。经过优化的 LLE 方法采用 0.1 M HCl 甲基叔丁基醚 (MTBE)(用浓盐酸酸化)对 200 μL 血液进行一次萃取,证明该方法适用于碱性和中性物质的萃取;重组溶剂为 88:12v/v, 0.1 % 甲酸与 10 mM 乙酸铵水溶液的混合物,pH 值为 3.5:0.1 % 甲酸与乙腈的混合物,所有分析物的回收率均令人满意。该方法灵敏度高,所有物质的最低检出限/最低限均较低,分别为 0.01 至 5 纳克/毫升/ 0.05 至 20 纳克/毫升。线性范围为 0.05-500 ng/mL(R2 = 0.9811-0.9995),日间和日内精确度分别为 3-15 % 和 7-18 %。准确度按回收率评估,在可接受范围内。所有分析物的基质效应(以离子抑制/增强表示)均在±25%的范围内。分析物的分离后稳定性高于 85%,运行之间无携带现象。所开发的方法已成功应用于常规毒理学分析,用于分析来自临床和尸检病例的生物样本。
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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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