Chen Lizhu, Yu Yingjia, Duan Gengli, Wang Xin, Shen Baohua, Xiang Ping
Shanghai Key Laboratory of Forensic Medicine, Department of Forensic Toxicology, Academy of Forensic Science, Shanghai, China.
Department of Pharmaceutical Analysis, School of Pharmacy, Fudan University, Shanghai, China.
Front Chem. 2019 Apr 17;7:248. doi: 10.3389/fchem.2019.00248. eCollection 2019.
Chiral analysis is a crucial method to differentiate selegiline intake from drug abuse. A dried urine spot (DUS) analytical method based on spotting urine samples (10 μL) onto dried spot collection cards, and followed by air-drying and extraction, was developed and validated for the determination of selegiline, desmethylselegiline, R/S-methamphetamine, and R/S-amphetamine. Methanol (0.5 mL) was found to be the ideal extraction solvent for target extraction from DUSs under orbital-horizontal stirring on a lateral shaker at 1,450 rpm for 30 min. Determinations were performed by direct electrospray ionization tandem mass spectrometry (ESI-MS/MS) under positive electrospray ionization conditions using multiple reaction monitoring mode. The chromatographic system consisted of a Chirobiotic V2 column (2.1 × 250 mm, 5 μm) and a mobile phase of methanol containing 0.1% (v/v) glacial acetic acid and 0.02% (v/v) ammonium hydroxide. The calibration curves were linear from 50 to 5,000 ng/mL, with > 0.995 for all analytes, imprecisions ≤ 15% and accuracies between -11.4 and 11.7%. Extraction recoveries ranged from 48.6 to 105.4% with coefficients of variation (CV) ≤ 13.7%, and matrix effects ranged from 45.4 to 104.1% with CV ≤ 10.3%. The lower limit of quantification was 50 ng/mL for each analyte. The present method is simple, rapid (accomplished in 12 min), sensitive, and validated by a pharmacokinetic study in human urine collected after a single oral administration of SG.
手性分析是区分司来吉兰摄入与药物滥用的关键方法。开发并验证了一种基于将尿液样本(10 μL)点样到干血斑采集卡上,然后进行风干和萃取的干尿斑(DUS)分析方法,用于测定司来吉兰、去甲基司来吉兰、R/S-甲基苯丙胺和R/S-苯丙胺。结果发现,甲醇(0.5 mL)是在横向振荡器上以1450 rpm的转速进行轨道水平搅拌30分钟从DUS中萃取目标物的理想萃取溶剂。在正电喷雾电离条件下,使用多反应监测模式通过直接电喷雾电离串联质谱(ESI-MS/MS)进行测定。色谱系统由Chirobiotic V2柱(2.1×250 mm,5 μm)和含有0.1%(v/v)冰醋酸和0.02%(v/v)氢氧化铵的甲醇流动相组成。校准曲线在50至5000 ng/mL范围内呈线性,所有分析物的相关系数>0.995,精密度≤15%,准确度在-11.4%至11.7%之间。萃取回收率在48.6%至105.4%之间,变异系数(CV)≤13.7%,基质效应在45.4%至104.1%之间,CV≤10.3%。每种分析物的定量下限为50 ng/mL。本方法简单、快速(12分钟内完成)、灵敏,并通过单次口服司来吉兰后收集的人尿药代动力学研究进行了验证。