Yang Chu-An, Liu Hsiu-Chuan, Lin Dong-Liang, Liu Ray H, Hsieh You-Zung, Wu Shu-Pao
Department of Applied Chemistry, National Chiao Tung University, 1001 University Road, Hsinchu 30010, Taiwan.
Department of Forensic Toxicology, Institute of Forensic Medicine, Ministry of Justice, No. 123, Min-An St., Zhonghe Dist., New Taipei City 23548, Taiwan.
J Anal Toxicol. 2017 Oct 1;41(8):679-687. doi: 10.1093/jat/bkx057.
Heroin, methamphetamine and ketamine have been the most commonly abused drugs in Taiwan. The presence of these drugs and their metabolites in postmortem specimens has been routinely monitored in our laboratory mostly by gas chromatographic-mass spectrometric methods. This study aimed to evaluate a more effective approach to simultaneously quantify these analytes (i.e., amphetamine, methamphetamine, 3,4-methylenedioxyamphetamine, 3,4-methylenedioxymethamphetamine (MDMA), morphine, codeine, 6-acetylmorphine, 6-acetylcodeine, ketamine and norketamine) in postmortem urine and blood specimens by liquid chromatography-tandem mass spectrometry (LC-MS-MS). Samples (1 mL) were extracted via solid-phase extraction, evaporated and reconstituted in the mobile phase for injection into the LC-MS-MS system. Respective deuterated analogs of these analytes were used as internal standards. Chromatographic separation was achieved by an Agilent Zorbax SB-Aq analytical column at 50°C. Mass spectrometric analysis was performed by electrospray ionization in positive-ion dynamic multiple reaction monitoring mode with optimized collision energy for respective precursor ion selected for each analyte, and the monitoring of two transition ions. Performance characteristics were assessed using drug-free samples that were fortified with 50-1,000 ng/mL of the 10 analytes. Analytical parameters evaluated and resulting data are as follows: (i) average extraction recoveries (n= 3) were better than 80%, except for MDMA (71%) and morphine (74%); (ii) inter-day and intra-day precision ranges (%CV) were 1.59-8.80% and 0.57-3.89%, respectively; (iii) calibration linearity (r2), detection limit and quantitation limit for all analytes were >0.999, 1 and 5 ng/mL, respectively; (iv) matrix effects (ion suppression) were observed for three analytes, but were satisfactorily compensated for by the deuterated internal standards adopted in the analytical protocol. This method was successfully applied to the analysis of specimens collected from unknown death cases from various district prosecutors' offices in Taiwan, and was also found helpful to understanding whether the detected opiates were derived from heroin or legal morphine/codeine-containing medications.
海洛因、甲基苯丙胺和氯胺酮一直是台湾地区最常被滥用的毒品。在我们实验室,主要通过气相色谱 - 质谱法对死后标本中这些毒品及其代谢物的存在情况进行常规监测。本研究旨在评估一种更有效的方法,通过液相色谱 - 串联质谱法(LC - MS - MS)同时定量死后尿液和血液标本中的这些分析物(即苯丙胺、甲基苯丙胺、3,4 - 亚甲基二氧基苯丙胺、3,4 - 亚甲基二氧基甲基苯丙胺(摇头丸)、吗啡、可待因、6 - 乙酰吗啡、6 - 乙酰可待因、氯胺酮和去甲氯胺酮)。取1 mL样品通过固相萃取进行提取,蒸发后再用流动相复溶,然后注入LC - MS - MS系统。这些分析物各自的氘代类似物用作内标。在50°C下,通过安捷伦Zorbax SB - Aq分析柱实现色谱分离。质谱分析采用电喷雾电离,在正离子动态多反应监测模式下进行,针对每种分析物选择的前体离子具有优化的碰撞能量,并监测两个跃迁离子。使用不含药物的样品进行性能特征评估,这些样品添加了浓度为50 - 1000 ng/mL的10种分析物。评估的分析参数及所得数据如下:(i)平均提取回收率(n = 3)除摇头丸(71%)和吗啡(74%)外均优于80%;(ii)日间和日内精密度范围(%CV)分别为1.59 - 8.80%和0.57 - 3.89%;(iii)所有分析物的校准线性(r2)、检测限和定量限分别>0.999、1 ng/mL和5 ng/mL;(iv)观察到三种分析物存在基质效应(离子抑制),但通过分析方案中采用的氘代内标得到了满意的补偿。该方法成功应用于台湾各地地方检察官办公室从不明死亡案件中收集的标本分析,并且还发现有助于了解检测到的阿片类药物是源自海洛因还是含合法吗啡/可待因的药物。