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液相色谱/超声喷雾电离质谱法测定对甲氧基苯丙胺及其他与苯丙胺有关的设计药物

Determination of paramethoxyamphetamine and other amphetamine-related designer drugs by liquid chromatography/sonic spray ionization mass spectrometry.

作者信息

Mortier Kjell A, Dams Riet, Lambert Willy E, De Letter Els A, Van Calenbergh Serge, De Leenheer André P

机构信息

Laboratorium voor Toxicologie, Universiteit Gent, Harelbekestraat 72, B-9000 Gent, Belgium.

出版信息

Rapid Commun Mass Spectrom. 2002;16(9):865-70. doi: 10.1002/rcm.657.

Abstract

Paramethoxyamphetamine (PMA) is an amphetamine-like designer drug that has emerged recently on the European illicit drug market. This drug has a wicked reputation, as a number of lethal intoxications have occurred. A method using high-performance liquid chromatography coupled to ion trap based mass spectrometry (LC/MS) is described for the determination of this compound together with 3,4-methylenedioxymethamphetamine (XTC or MDMA), amphetamine and 3,4-methylenedioxyamphetamine (MDA) in human matrices. A liquid/liquid extraction (LLE) was applied to whole blood, urine and postmortem tissues. Reversed-phase liquid chromatography was performed on a narrow-bore phenyl-type column at a flow rate of 0.3 mL/min. A switch box allowed disposal of early-eluting irrelevant material to waste, protecting the mass spectrometer from contamination. The column effluent was directed into an ion trap mass spectrometer by a sonic spray ionization (SSI) interface. The method was validated for all three matrices, proving the applicability of SSI even when dealing with complex biological matrices. The within-and between-day precisions were less than 17.5% and accuracy was below 16.2%. Weighted (1/x) quadratic calibration curves were generated ranging from 10 to 1000 ng/mL (blood and urine) or 20 to 2000 ng/g (tissue) and correlation coefficients (r(2)) always exceeded 0.995. In addition, the mass spectrum of PMA is given together with a proposed fragmentation pattern for the obtained LC/MS spectrum. This information can be useful for future identification of PMA with LC/MS in biological matrices as well as in confiscated powders or tablets.

摘要

对甲氧基苯丙胺(PMA)是一种类似苯丙胺的合成毒品,最近出现在欧洲非法毒品市场上。这种毒品声名狼藉,已经发生了多起致命中毒事件。本文描述了一种使用高效液相色谱与基于离子阱的质谱联用(LC/MS)的方法,用于测定人体样本中的该化合物以及3,4-亚甲基二氧基苯丙胺(摇头丸或MDMA)、苯丙胺和3,4-亚甲基二氧基苯丙胺(MDA)。采用液-液萃取(LLE)法处理全血、尿液和死后组织。在窄孔苯基型柱上以0.3 mL/min的流速进行反相液相色谱分析。一个切换盒可将早期洗脱的无关物质排至废液,保护质谱仪不受污染。柱流出物通过超声喷雾电离(SSI)接口导入离子阱质谱仪。该方法在所有三种样本基质中均得到验证,证明了即使处理复杂生物基质时SSI的适用性。日内和日间精密度均小于17.5%,准确度低于16.2%。生成了加权(1/x)二次校准曲线,范围为10至1000 ng/mL(血液和尿液)或20至2000 ng/g(组织),相关系数(r²)始终超过0.995。此外,还给出了PMA的质谱图以及所获得的LC/MS谱图的拟碎片模式。这些信息对于未来在生物基质以及没收的粉末或片剂中用LC/MS鉴定PMA可能会有用。

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