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一种用于测定口腔液中3,4-亚甲基二氧甲基苯丙胺(摇头丸)的高速基质辅助激光解吸电离串联四极杆质谱法的开发。

Development of a high-speed MALDI-triple quadrupole mass spectrometric method for the determination of 3,4-methylenedioxymethamphetamine (MDMA) in oral fluid.

作者信息

Poetzsch Michael, Steuer Andrea E, Hysek Cedric M, Liechti Matthias E, Kraemer Thomas

机构信息

Department of Forensic Pharmacology and Toxicology, ZIFM - Zurich Institute of Forensic Medicine, University of Zurich, Zurich, Switzerland.

Departement of Biomedicine, Division of Clinical Pharmacology and Toxicology, University Hospital Basel, University of Basel, Basel, Switzerland.

出版信息

Drug Test Anal. 2016 Feb;8(2):235-40. doi: 10.1002/dta.1810. Epub 2015 May 19.

DOI:10.1002/dta.1810
PMID:25990956
Abstract

3,4-Methylenedioxymethamphetamine (MDMA, ecstasy) is still a widely used illicit designer drug and its detection in different matrices is of major importance for forensic purposes (e.g. driving under the influence) as well as for workplace drug testing or abstinence control. Established analytical methods for the determination of MDMA are mainly employing high performance liquid chromatography (HPLC) or gas chromatography (GC) coupled to mass spectrometric detection. Matrix assisted laser desorption/ionization-triple quadrupole-tandem mass spectrometry (MALDI-QqQ-MS/MS) is so far rarely used in forensics and offers an ultrafast high-throughput platform. The Quantisal™ Oral Fluid Collection Device was used for sample collection. After addition of the deuterated internal standard and a carbonate buffer (0.75 M Na2 CO3 ), oral fluid samples were liquid-liquid extracted (ButOAc/EtOAc, 1:1). As little as 1 microlitre of a mixture of this extract and the MALDI matrix (alpha-cyano-4-hydroxycinnamic acid) was spotted onto the MALDI plate and could directly be analyzed. With MALDI omitting chromatographic separation, very short analysis times of about 10 s per sample were possible. The method was developed and validated according to international guidelines including specificity, recovery, matrix effects, accuracy and precision, stabilities and limit of quantification. All validation criteria were fulfilled except for ion suppression/enhancement. Comparison with a routine liquid chromatography-tandem mass spectrometry (LC-MS/MS) method showed good agreement of the results. Applicability of the method was shown by analyzing about 250 oral fluid samples collected after controlled administration of 125 mg MDMA in a pharmacokinetic study. The whole lot of samples could be analyzed in less than 1 h, proving the ultra-high-speed of the method.

摘要

3,4-亚甲基二氧甲基苯丙胺(摇头丸)仍是一种广泛使用的非法合成毒品,在不同基质中检测到它对于法医鉴定(如酒驾)以及职场药物检测或戒毒管控至关重要。已有的测定摇头丸的分析方法主要采用高效液相色谱(HPLC)或气相色谱(GC)与质谱检测联用。基质辅助激光解吸/电离-三重四极杆-串联质谱(MALDI-QqQ-MS/MS)迄今为止在法医鉴定中很少使用,但它提供了一个超快速高通量平台。使用Quantisal™口腔液采集装置进行样本采集。加入氘代内标和碳酸盐缓冲液(0.75 M Na2CO3)后,对口腔液样本进行液-液萃取(乙酸丁酯/乙酸乙酯,1:1)。将仅1微升的该萃取物与MALDI基质(α-氰基-4-羟基肉桂酸)的混合物点样到MALDI板上,即可直接进行分析。由于MALDI无需色谱分离,每个样本的分析时间可短至约10秒。该方法按照国际指南进行开发和验证,包括特异性、回收率、基质效应、准确度和精密度、稳定性以及定量限。除离子抑制/增强外,所有验证标准均已满足。与常规液相色谱-串联质谱(LC-MS/MS)方法的比较表明结果吻合良好。在一项药代动力学研究中,通过分析在服用125毫克摇头丸后采集的约250份口腔液样本,证明了该方法的适用性。所有样本能够在不到1小时内完成分析,证明了该方法的超高速特性。

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