Alsenedi Khalid A, Morrison Calum
Forensic Medicine and Science, School of Medicine, Dentistry and Nursing, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, United Kingdom.
J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Feb 15;1076:91-102. doi: 10.1016/j.jchromb.2018.01.027.
A method was developed for the screening and quantification of seven amphetamine-type stimulants (ATS) and 22 cathinones, including three metabolites, in urine with Gas Chromatography-Mass Spectrometry. This method allowed the detection and quantification of ATS and cathinones group molecules using one procedure. A study of the stability of the drug mixtures for a period of 201 days in human urine samples under three different conditions has been carried. The ATS and cathinones include amphetamine, methamphetamine, MDA, MDEA, MDMA, PMA, PMMA, cathinone, methcathinone, 3'-position-substituted, ring-substituted, methylenedioxy-substituted, N-alkyl-substituted and pyrrolidinyl-substituted. Twenty drugs out of twenty-nine were validated with a quantitative method. This method can be applied to the nine remaining drugs as a screening method. The linearity of the assay was from 50 to 2000 ng/ml, with limits of detection of 0.5 to 10 ng/ml. In terms of accuracy, between-run and within-run precision were ≤20% for 20 compounds with good selectivity. No carryover was seen, and the recovery was between 80 and 120% for most drugs tested. ATS and pyrrolidinyl-substituted groups were conducted to be stable compounds under all conditions. All compounds tested were stable at -20 °C. Some cathinones were primarily degraded after 21 days at 4 °C. They were detectable but unstable after 201 days at 4 °C. Most cathinones were unstable after a day and completely lost after 28 days at RT.
开发了一种采用气相色谱 - 质谱法筛查和定量尿液中七种苯丙胺类兴奋剂(ATS)和22种卡西酮(包括三种代谢物)的方法。该方法可通过一个程序检测和定量ATS和卡西酮类分子。对药物混合物在三种不同条件下于人类尿液样本中201天的稳定性进行了研究。ATS和卡西酮包括苯丙胺、甲基苯丙胺、MDA、MDEA、MDMA、PMA、PMMA、卡西酮、甲基卡西酮、3'-位取代、环取代、亚甲二氧基取代、N-烷基取代和吡咯烷基取代的化合物。29种药物中的20种通过定量方法进行了验证。该方法可作为筛查方法应用于其余9种药物。该检测方法的线性范围为50至2000 ng/ml,检测限为0.5至10 ng/ml。在准确性方面,20种具有良好选择性的化合物的批间和批内精密度≤20%。未观察到残留,大多数测试药物的回收率在80%至120%之间。结果表明,ATS和吡咯烷基取代的化合物在所有条件下均为稳定化合物。所有测试化合物在-20°C下均稳定。一些卡西酮在4°C下21天后主要降解。在4°C下201天后它们仍可检测到但不稳定。大多数卡西酮在室温下一天后不稳定,28天后完全消失。