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利用液相色谱-串联质谱法鉴定和定量死后全血中的六十种药物及其代谢物的方法。

Method for the identification and quantification of sixty drugs and their metabolites in postmortem whole blood using liquid chromatography tandem mass spectrometry.

机构信息

King Abdulaziz Hospital, Jeddah, Makkah Al-Mukharma, Saudi Arabia.

出版信息

Forensic Sci Int. 2020 Apr;309:110193. doi: 10.1016/j.forsciint.2020.110193. Epub 2020 Feb 11.

DOI:10.1016/j.forsciint.2020.110193
PMID:32142991
Abstract

The aim of this work was to develop and validate a liquid chromatography tandem mass spectrometry method for detecting sixty drugs and metabolites that are most commonly encountered in postmortem whole blood analysis. Although a large number of drugs were included in the panel, acceptance criteria for method validation were achieved. All calibration curves were found to be linear with coefficients of determination greater than 0.99. The limits of detection ranged from 0.2ng/mL to 1.0ng/mL and the limits of quantification range from 1.0ng/mL to 5.0ng/mL. Using three controls, within-run precision was 0.7%-10.3% and between-run precision was 0.6%-9.0%. Accuracy was ranged from 95.0%-104.1%. Matrix effects ranged from -15% to +22%. After excluding matrix effects, analytical recoveries ranged from 76% to 100%. Coefficients of variation for matrix effects ranged from 0.5%-13% and coefficients of variation for recovery ranged from 0.9%-13.0%. Over 1000 postmortem blood samples were analyzed. Among them, 435 cases (45%) tested positive for at least one analyte of interest. In conclusion, this study presents a technique for multianalyte screening of sixty drugs and metabolites that are commonly encountered in postmortem toxicology. This technique was then applied in routine analysis of autopsy blood samples in order to assess the applicability of this method. Data from postmortem cases is rarely reported from Saudi Arabia, and one of the current study goals is to present new information from postmortem cases to help prevent wide-spread drug use.

摘要

本研究旨在建立并验证一种液相色谱-串联质谱法,用于检测 60 种最常用于死后全血分析的药物和代谢物。虽然该检测panel 中包含了大量药物,但仍达到了方法验证的接受标准。所有的校准曲线均具有良好的线性,决定系数大于 0.99。检测限范围为 0.2ng/mL 至 1.0ng/mL,定量限范围为 1.0ng/mL 至 5.0ng/mL。使用三个质控品,批内精密度为 0.7%-10.3%,批间精密度为 0.6%-9.0%。准确度在 95.0%-104.1%之间。基质效应范围为-15%至+22%。排除基质效应后,分析回收率范围为 76%-100%。基质效应的变异系数范围为 0.5%-13%,回收率的变异系数范围为 0.9%-13.0%。对 1000 多份死后血样进行了分析。其中,435 例(45%)至少有一种感兴趣的分析物呈阳性。总之,本研究提出了一种用于检测死后毒理学中常见的 60 种药物和代谢物的多分析物筛选技术。然后,该技术被应用于常规分析尸检血样,以评估该方法的适用性。来自沙特阿拉伯的死后案例数据很少有报道,本研究的目标之一是提供来自死后案例的新信息,以帮助预防广泛的药物使用。

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