Björnstad Kristian, Beck Olof, Helander Anders
Department of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden.
J Chromatogr B Analyt Technol Biomed Life Sci. 2009 Apr 15;877(11-12):1162-8. doi: 10.1016/j.jchromb.2009.03.004. Epub 2009 Mar 11.
A sensitive and specific LC-MS/MS method for simultaneous detection of 10 plant-derived psychoactive substances (atropine, N,N-dimethyltryptamine, ephedrine, harmaline, harmine, ibogaine, lysergic acid amide, psilocin, scopolamine and yohimbine) in urine was developed. Direct injection of urine diluted with 3 deuterated internal standards allowed for a readily accessible method suitable for application in clinical intoxication cases. Separation was achieved using reversed phase chromatography and gradient elution with a total analysis time of 14 min. Electrospray ionization was used and ions were monitored in the positive selected reaction monitoring mode. The calibration curves were linear (r(2)>0.999) and the total imprecision at high (1000 microg/L) and low (50 microg/L) substance concentrations were 4.9-13.8% and 8.3-26%, respectively. Infusing the analytes post column and injecting matrix samples showed limited influence by ion suppression. The multi-component method proved to be useful for investigation of authentic cases of intoxication with plant-derived psychoactive drugs and was indicated to cover the clinically relevant concentration ranges.
建立了一种灵敏且特异的液相色谱-串联质谱法,用于同时检测尿液中的10种植物源性精神活性物质(阿托品、N,N-二甲基色胺、麻黄碱、骆驼蓬碱、哈尔明碱、伊博格碱、麦角酰胺、裸盖菇素、东莨菪碱和育亨宾)。直接进样经3种氘代内标物稀释的尿液,得到了一种适用于临床中毒病例的便捷方法。采用反相色谱和梯度洗脱实现分离,总分析时间为14分钟。使用电喷雾电离,在正离子选择反应监测模式下监测离子。校准曲线呈线性(r(2)>0.999),在高(1000μg/L)、低(50μg/L)物质浓度下的总不精密度分别为4.9 - 13.8%和8.3 - 26%。柱后注入分析物和进样基质样品显示离子抑制影响有限。该多组分方法被证明对植物源性精神活性药物中毒真实病例的调查有用,并表明涵盖了临床相关浓度范围。