Determination of illicit drugs and their metabolites in human urine by liquid chromatography tandem mass spectrometry including relative ion intensity criterion

被引:29
作者
Concheiro, Marta [1 ]
De Castro, Ana [1 ]
Quintela, Oscar [1 ]
Cruz, Angelines [1 ]
Lopez-Rivadulla, Manuel [1 ]
机构
[1] Univ Santiago de Compostela, Forens Toxicol Serv, Santiago De Compostela, Spain
关键词
D O I
10.1093/jat/31.9.573
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method, using 0.5 mL of urine, was developed for the simultaneous determination of ecgonine methyl ester, benzoylecgonine, morphine, codeine, 6-acetylmorphine, amphetamine, methamphetamine, 3,4-methylenedioxyamphetamine (MDA), 3,4-methylenedioxymethamphetamine (MDMA), methadone, 2-ethylidene-1,5- dimethyl-3,3-diphenylpyrrolidine (EDDP), and d-lysergic acid diethylamide (LSD). The analysis was performed by liquid chromatography with tandem mass spectrometry, after solid-phase extraction in the presence of their deuterated analogues. Reversed-phase separation on an Atlantis dC18 column was achieved in 12.5 min, under gradient conditions. The method was fully validated, including linearity (1-2000 μg/L for ecgonine methyl ester, benzoylecgonine, 6-acetylmorphine, methamphetamine, MDMA, and EDDP; 2-2000 μg/L for morphine, codeine, MDA, and methadone; 2-1000 μg/L for amphetamine, and 0.2-100 μg/L for LSD; r2 > 0.99); recovery (> 65%), within-day and between-day precision, and accuracy (CV and MRE < 15%); limit of detection (0.1 μg/L for LSD, 0.5 μg/L for ecgonine methyl ester, benzoylecgonine, methamphetamine, MDMA, 6-monoacetylmorphine, and EDDP, and 1 μg/L for amphetamine, MDA, morphine, and methadone); quantitation (lowest level of the calibration curve); relative ion intensities, freeze-and-thaw stability, and matrix effect. The procedure showed to be sensitive and specific, and was applied to real cases and quality control samples from a quality control program.
引用
收藏
页码:573 / 580
页数:8
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