Makhdoom Humera Shafi, Afzal Saira, Sultana Kishwar, Shah Syed Nisar Hussain, Mujahid Majida, Hassan Zulfiqar Ul, Munir Farida, Jahan Faryal, Abbas Zeerak, Abid Ali Imran, Khan Najm Ul Hassan
Faculty of Pharmacy, University of Lahore, Lahore 44000, Pakistan.
Clinical and Forensic Toxicology Department, Chughtai Healthcare, Lahore 54000, Pakistan.
ACS Omega. 2024 May 22;9(22):23355-23363. doi: 10.1021/acsomega.3c09669. eCollection 2024 Jun 4.
An increase in cocaine abuse has been observed globally since the past decade. Cocaine is among the commonly abused stimulants used for recreational purposes. In this study, the SPE-UHPLC-MS/MS method was developed and validated to be applied on real specimens of 20 chronic cocaine abusers to quantify cocaine/metabolites in conventional as well as alternative biological matrices. Cocaine was extracted from biological specimens using solid-phase extraction followed by liquid chromatography tandem mass spectrometry analysis. Chromatographic separation was achieved on a Poroshell120EC-18 column (2.1 mm × 50 mm, 2.7 μm particle size) using water-acetonitrile in 0.1% formic acid as a mobile phase in gradient elution mode. The flow rate of the mobile phase was 0.5 mL/min with a gradient varying the percentage of acetonitrile linearity ranging 15-95% in 6.0 min acquisition time, and the injection volume was set at 5 μL. Positive electrospray ionization with multireaction ion monitoring mode using two ion transitions for cocaine/metabolites and one for cocaine-d3 was employed. The quantification method demonstrated good linear ranges of 0.025-250 ng/mL in blood, urine, and oral fluid (ng/mg for hair and nail) with a ≥0.991% determination coefficient. The detection limit and lower quantification limit were 0.005 and 0.025 ng/mL in all matrices, respectively. The mean extraction recovery and ionization suppression ranged from 89.3 to 99.8% and -4.6 to -14.4% in the studied matrices. Within-run and between-days precisions were 1.8-7.2% and 1.9-6.1%, respectively. This study will not only help in quantifying cocaine/metabolites in alternative specimens (hair, nail, and oral fluid) but also guide clinical and forensic toxicologists in interpretation of exhumation cases. Furthermore, multiple specimens' analyses can be of significance in estimating the time/manner of drug exposure, in confirming the results of laboratories in cases of doubtful clinical histories, or in aiding medico-legal investigations.
自过去十年以来,全球可卡因滥用现象呈上升趋势。可卡因是常用于娱乐目的的常见滥用兴奋剂之一。在本研究中,开发并验证了固相萃取-超高效液相色谱-串联质谱法(SPE-UHPLC-MS/MS),用于分析20名慢性可卡因滥用者的实际样本,以定量常规及其他生物基质中的可卡因/代谢物。使用固相萃取从生物样本中提取可卡因,随后进行液相色谱串联质谱分析。采用Poroshell120EC-18柱(2.1 mm×50 mm,粒径2.7μm)进行色谱分离,以含0.1%甲酸的水-乙腈为流动相,采用梯度洗脱模式。流动相流速为0.5 mL/min,在6.0 min的采集时间内,乙腈百分比线性变化范围为15%-95%,进样量设定为5μL。采用正电喷雾电离和多反应离子监测模式,对可卡因/代谢物使用两个离子跃迁,对可卡因-d3使用一个离子跃迁。该定量方法在血液、尿液和口腔液中的线性范围良好,为0.025-250 ng/mL(毛发和指甲为ng/mg),测定系数≥0.991%。所有基质中的检测限和定量下限分别为0.005和0.025 ng/mL。在所研究的基质中,平均提取回收率和电离抑制率分别为89.3%-99.8%和-4.6%至-14.4%。批内精密度和日间精密度分别为1.8%-7.2%和1.9%-6.1%。本研究不仅有助于定量其他样本(毛发、指甲和口腔液)中的可卡因/代谢物,还可为临床和法医毒理学家解读尸体挖掘案件提供指导。此外,对多个样本的分析对于估计药物暴露的时间/方式、在临床病史存疑的情况下确认实验室结果或协助法医调查可能具有重要意义。