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采用液相色谱-串联质谱法对143种新型精神活性物质进行简单快速的筛查程序。

Simple and rapid screening procedure for 143 new psychoactive substances by liquid chromatography-tandem mass spectrometry.

作者信息

Adamowicz Piotr, Tokarczyk Bogdan

机构信息

Institute of Forensic Research, Westerplatte 9, 31-033, Krakow, Poland.

出版信息

Drug Test Anal. 2016 Jul;8(7):652-67. doi: 10.1002/dta.1815. Epub 2015 May 14.

DOI:10.1002/dta.1815
PMID:25976069
Abstract

In recent years, many new psychoactive substances (NPS) from several drug classes have appeared on the drug market. These substances, also known as 'legal highs', belong to different chemical classes. Despite the increasing number of NPS, there are few comprehensive screening methods for their detection in biological specimens. In this context, the purpose of this study was to develop a fast and simple liquid chromatography-tandem mass spectrometry (LC-MS/MS) screening procedure for NPS in blood. The elaborated method allows the simultaneous screening of 143 compounds from different groups (number of compounds): cathinones (36), phenethylamines (26), tryptamines (18), piperazines (9), piperidines (2), synthetic cannabinoids (34), arylalkylamines (7), arylcyclohexylamines (3), aminoindanes (2), and other drugs (6). Blood samples (0.2 mL) were precipitated with acetonitrile (0.6 mL). The separation was achieved with gradient mobile phase of 0.1% formic acid in acetonitrile and 0.1% formic acid in water in 14 min. Detection of all compounds was based on multiple reaction monitoring (MRM) transitions. The total number of transitions monitored in dynamic mode was 432. The whole procedure was rapid and simple. The limits of detection (LODs) estimated for 104 compounds were in the range 0.01-3.09 ng/mL. The extraction recoveries determined for 32 compounds were from 1.8 to 133%. The procedure was successfully applied to the analysis of forensic blood samples in routine casework. The developed method should have wide applicability for rapid screening of new drugs of abuse in forensic or clinical samples. The procedure can be easily expanded for more substances. Copyright © 2015 John Wiley & Sons, Ltd.

摘要

近年来,来自多个药物类别的许多新型精神活性物质(NPS)出现在毒品市场上。这些物质也被称为“合法兴奋剂”,属于不同的化学类别。尽管新型精神活性物质的数量不断增加,但在生物样本中检测它们的综合筛查方法却很少。在此背景下,本研究的目的是开发一种快速简便的液相色谱-串联质谱(LC-MS/MS)筛查程序,用于检测血液中的新型精神活性物质。精心制定的方法可同时筛查来自不同组别的143种化合物(化合物数量):卡西酮(36种)、苯乙胺(26种)、色胺(18种)、哌嗪(9种)、哌啶(2种)、合成大麻素(34种)、芳基烷基胺(7种)、芳基环己胺(3种)、氨基茚满(2种)和其他药物(6种)。取0.2 mL血液样本,用0.6 mL乙腈沉淀。在14分钟内,使用乙腈中0.1%甲酸和水中0.1%甲酸的梯度流动相实现分离。所有化合物的检测均基于多反应监测(MRM)转换。动态模式下监测的转换总数为432个。整个过程快速简便。104种化合物的估计检测限(LOD)在0.01 - 3.09 ng/mL范围内。32种化合物的萃取回收率在1.8%至133%之间。该程序已成功应用于常规案件工作中的法医血液样本分析。所开发的方法在法医或临床样本中快速筛查新型滥用药物方面应具有广泛的适用性。该程序可以很容易地扩展到更多物质。版权所有© 2015约翰威立父子有限公司。

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