Imbert L, Dulaurent S, Mercerolle M, Morichon J, Lachâtre G, Gaulier J-M
Department of Pharmacology and Toxicology, University Hospital, 2, Avenue Martin-Luther-King, 87042 Limoges Cedex, France.
Department of Pharmacology and Toxicology, University Hospital, 2, Avenue Martin-Luther-King, 87042 Limoges Cedex, France; Laboratory of Toxicology, Faculty of Pharmacy, 2 rue Docteur Raymond Marcland, 87000 Limoges, France.
Forensic Sci Int. 2014 Jan;234:132-8. doi: 10.1016/j.forsciint.2013.11.004. Epub 2013 Nov 15.
The two major challenges in hair analysis are the limited amount of samples usually available and the low targeted concentrations. To overcome these limitations, a liquid chromatography-electrospray-tandem mass spectrometry method (LC-ESI-MS/MS) allowing the simultaneous analysis of 17 amphetamines (amphetamine, BDB, m-CPP, dexfenfluramine, DOB, DOM, ephedrine, MBDB, MDA, MDEA, MDMA, methamphetamine, methylphenidate, 4-MTA, norephedrine, norfenfluramine and PMA), 5 opiates (morphine, codeine, heroin, ethylmorphine, and 6AM), cocaine and 5 metabolites [ecgonine methyl ester (EME), benzoylecgonine (BZE), anhydroecgonine methyl ester (AME), cocaethylene, and norcocaine] has been developed. The validation procedure included linearity, intra-day and inter-day variability and accuracy for 5 days (5 replicates at 3 concentration levels). Proficiency studies were used to check the accuracy of the method. As a result, all amphetamines, opiates and cocaine derivatives were satisfactory identified by 2 MRM transitions in 15 min. Calibration curves were performed by a quadratic 1/X weighted regression. The calibration model fits from 0.05 to 10 ng/mg. The limits of detection (LODs) range between 0.005 and 0.030 ng/mg. Precision has been checked by intra-day and inter-day RSD, and associated relative bias, which were lower than 25% for the limits of quantifications (LOQs) and lower than 20% for the other levels tested. This method was routinely applied to hair samples: two positive results of adult drug addicts are presented.
毛发分析中的两大主要挑战是通常可获得的样本量有限以及目标浓度较低。为克服这些限制,已开发出一种液相色谱 - 电喷雾串联质谱法(LC - ESI - MS/MS),该方法可同时分析17种苯丙胺类药物(苯丙胺、BDB、间氯苯丙胺、右芬氟拉明、DOB、DOM、麻黄碱、MBDB、MDA、MDEA、摇头丸、甲基苯丙胺、哌醋甲酯、4 - MTA、去甲麻黄碱、去甲芬氟拉明和PMA)、5种阿片类药物(吗啡、可待因、海洛因、乙基吗啡和6 - AM)、可卡因及5种代谢物[芽子碱甲酯(EME)、苯甲酰芽子碱(BZE)、脱水芽子碱甲酯(AME)、可卡因乙烯酯和去甲可卡因]。验证程序包括线性、日内和日间变异性以及5天的准确度(在3个浓度水平下进行5次重复)。采用能力验证研究来检验该方法的准确性。结果表明,所有苯丙胺类药物、阿片类药物和可卡因衍生物均可在15分钟内通过2次多反应监测(MRM)转换得到满意鉴定。校准曲线通过二次1/X加权回归进行。校准模型在0.05至10 ng/mg范围内拟合良好。检测限(LOD)在0.005至0.030 ng/mg之间。通过日内和日间相对标准偏差(RSD)以及相关相对偏差来检查精密度,对于定量限(LOQ),其低于25%,对于其他测试水平,其低于20%。该方法已常规应用于毛发样本:展示了两名成年吸毒者的阳性检测结果。