Fast LC-MS/MS method for the determination of amphetamine, methamphetamine, MDA, MDMA, MDEA, MBDB and PMA in urine

被引:70
作者
Concheiro, Marta
Sadler Simoes, Susana Maria dos Santos
Quintela, Oscar
de Castro, Ana
Rodrigues Dias, Mario Joao
Cruz, Angelines
Lopez-Rivadulla, Manuel
机构
[1] Univ Santiago de Compostela, Inst Med Legale, Forens Toxicol Serv, Santiago De Compostela 15782, Spain
[2] Natl Inst Legal Med, Forens Toxicol Serv, Lisbon Dept, P-1169201 Lisbon, Portugal
关键词
amphetamine; MDMA; PMA; LC-MS/MS; urine;
D O I
10.1016/j.forsciint.2006.10.004
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
A fast method was designed for the simultaneous determination of amphetamine (A), methamphetamine (MA), PMA, MDA, MDMA, MDEA and MBDB in urine. The drugs were analysed by LC (ESI)-MS/MS, after a simple liquid-liquid extraction in the presence of the deuterated analogues. Reverse phase separation on an Atlantis dC 18 Intelligent Speed column was achieved in less than 4 min under gradient conditions, and the total run time was 8 min. The method was fully validated, including linearity (1-1000 ng/mL for A, MDMA, MDEA and MBDB; 2-1000 ng/ mL for MDA and PMA; 1-200 ng/mL for MA; r(2) > 0.99 for all compounds), recovery (> 80%), within-day and between-day precision and accuracy (CV and MRE < 12.7% for intermediate level and ULOQ, and < 17.2% for LLOQ), limit of detection (0.2 ng/mL for MDMA, MDEA and MBDB; 0.5 ng/mL for A, MA and PMA; 1 ng/mL for MDA) and quantitation (1 ng/mL for A, MA, MDMA, MDEA and MBDB; 2 ng/mL for MDA and PMA) and relative ion intensities. No matrix effect was observed. The procedure proved to be sensitive, specific and rapid, and was applied to real forensic cases. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:44 / 51
页数:8
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