Sergi M, Bafile E, Compagnone D, Curini R, D'Ascenzo G, Romolo F S
Department of Food Science, University of Teramo, Via C. R. Lerici 1, Mosciano S.A., 64023, Teramo, Italy.
Anal Bioanal Chem. 2009 Jan;393(2):709-18. doi: 10.1007/s00216-008-2456-3. Epub 2008 Nov 4.
An analytical procedure for the simultaneous determination in human plasma and oral fluids of several illicit drugs belonging to different chemical and toxicological classes is presented. Amphetamine, methamphetamine, morphine, 6-monoacetylmorphine, methylenedioxyamphetamine, methylenedioxyethylamphetamine, methylenedioxymethamphetamine, cocaine, benzoylecgonine, tetrahydrocannabinol, carboxytetrahydrocannabinol, ketamine, and phencyclidine have been quantified in real samples using a very rapid sample treatment, basically a protein precipitation. The quantitative analysis was performed by liquid chromatography-tandem mass spectrometry and has been fully validated. All the analytes were detected in positive ionization mode using a TurboIonSpray source, except carboxytetrahydrocannabinol, which was detected in negative ionization mode. The use of a diverter valve between the column and the mass spectrometer allows the preservation of the ion source performances for high-throughput analysis.
本文介绍了一种同时测定人血浆和口腔液中几种属于不同化学和毒理学类别的非法药物的分析方法。使用非常快速的样品处理方法(基本上是蛋白质沉淀法)对苯丙胺、甲基苯丙胺、吗啡、6-单乙酰吗啡、亚甲二氧基苯丙胺、亚甲二氧基乙基苯丙胺、亚甲二氧基甲基苯丙胺、可卡因、苯甲酰芽子碱、四氢大麻酚、羧基四氢大麻酚、氯胺酮和苯环利定在实际样品中进行了定量分析。通过液相色谱-串联质谱法进行定量分析,并已得到充分验证。除羧基四氢大麻酚在负离子模式下检测外,所有分析物均使用TurboIonSpray源在正离子模式下检测。在柱和质谱仪之间使用分流阀可保持离子源性能以进行高通量分析。