Department of Physical and Analytical Chemistry, Faculty of Experimental Sciences, University of Jaén, Jaén, Spain.
J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Jul 15;879(22):2034-42. doi: 10.1016/j.jchromb.2011.05.034. Epub 2011 May 30.
In this work, an automated screening method for the simultaneous identification and quantitation of 30 representative multiclass drugs (including opiates, cocaine and its main metabolite, cannabinoids, amphetamines and other stimulants in hair samples) has been developed using fast liquid-chromatography time-of-flight mass spectrometry (LC-TOFMS). The identification and quantitation of the drugs were carried out by liquid chromatography using a C(18) column (4.6×50 mm) with 1.8 μm particle size. Accurate mass measurements of ions of interest (typically M+H) by electrospray time-of-flight mass spectrometry in the positive ionization mode were used for unambiguous confirmation of the targeted species. Three sample preparation methodologies were evaluated: (a) direct methanolic extraction by sonication, (b) acidic extraction, and (c) alkaline digestion. Direct methanolic extraction showed better recoveries and cleaner extracts. The limits of detection obtained in hair matrix were as low as 5 pg mg(-1) for cocaine and cannabidiol, ranging from 5 to 75 pg mg(-1) for the studied species while the LOQ ranged from 15 to 250 pg mg(-1). The method has been applied to six hair samples from drug consumer volunteers, where the presence of at least one drug was confirmed by accurate mass measurements within 2 ppm (mass error) in most cases. The present study demonstrates the usefulness of LC-TOFMS for both screening and quantitation purposes in drug testing in hair. In addition, the possibility of non-target or a posteriori data analysis of samples or the extension of the procedure for testing for additional compounds offers interesting features for forensic analysis.
本工作采用快速液相色谱飞行时间质谱(LC-TOFMS)建立了一种自动化筛选方法,用于同时鉴定和定量分析 30 种代表性多类药物(包括毛发样品中的阿片类药物、可卡因及其主要代谢物、大麻素、苯丙胺和其他兴奋剂)。采用 C(18)柱(4.6×50mm)和 1.8μm 粒径进行液相色谱,对药物进行鉴定和定量。采用电喷雾飞行时间质谱在正离子模式下对感兴趣的离子(通常为[M+H](+))进行精确质量测量,用于对目标物质进行明确确认。评估了三种样品制备方法:(a)直接甲醇超声提取,(b)酸性提取和(c)碱性消解。直接甲醇提取显示出更好的回收率和更清洁的提取物。在毛发基质中获得的检测限低至 5pgmg(-1),可卡因和大麻二酚的检测限为 5-75pgmg(-1),而研究物质的定量下限范围为 15-250pgmg(-1)。该方法已应用于 6 名药物消费者志愿者的毛发样本,在大多数情况下,通过精确质量测量在 2ppm(质量误差)内确认了至少一种药物的存在。本研究证明了 LC-TOFMS 在毛发药物检测中的筛选和定量目的的有用性。此外,对样品进行非靶向或事后数据分析或扩展检测其他化合物的程序的可能性为法医分析提供了有趣的特征。