Simultaneous quantification of amphetamine, opiates, ketamine and relative metabolites in urine for confirmatory analysis by liquid chromatography tandem mass spectrometry

被引:39
作者
Lin, Huei-Ru [1 ,2 ,3 ]
Choi, Ka-Ian [1 ]
Lin, Tzu-Chieh [3 ]
Hu, Anren [1 ,2 ,3 ]
机构
[1] Tzu Chi Univ, Dept Lab Med & Biotechnol, Hualien 970, Taiwan
[2] Tzu Chi Univ, Inst Med Biotechnol, Hualien 970, Taiwan
[3] Tzu Chi Univ, Ctr Drug Anal, Hualien 970, Taiwan
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2013年 / 929卷
关键词
Superficially porous liquid chromatography; Liquid chromatography tandem mass spectrometry; Confirmatory assay; Amphetamine; Opiates; Ketamine; LC-MS-MS; GAS-CHROMATOGRAPHY; ILLICIT DRUGS; IDENTIFICATION; ABUSE; PARTICLES; VALIDITY; MORPHINE; CRITERIA; CODEINE;
D O I
10.1016/j.jchromb.2013.03.022
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The rise in amphetamine, ketamine and opiates abuse in Taiwan has created a need for a reliable confirmatory assay. A method that combines superficially porous liquid chromatography tandem mass spectrometry (LC-MS/MS) with solid-phase extraction (SPE) was developed for the simultaneous quantification of amphetamine, 3,4-methylenedioxymethamphetamine (MDMA), ketamine, opiates, and their corresponding metabolites in urine. The total run time of the method was 6.7 min including equilibration time. The method was validated in accordance with the European Commission (EC) Decision 2002/642/EC. The within- and between-day precision was below 13.6% and the accuracy ranged from -17.1% to +9.9% for all analytes. Ion suppression was observed but compensated by using deuterated internal standards. No carryover was detected and the analytes were stable at room temperature for 16 h, and for 72 h at 4 degrees C, and three-thaw cycles. The method was further validated by comparison with a reference gas chromatography-mass spectrometry (GC-MS) method, using 52 authentic urine samples. The results indicated that for the target analytes studied, the LC-MS/MS analysis was as precise, accurate, and specific as the GC-MS method. In conclusion, the present LC-MS/MS method is robust and reliable, and suitable for use as a confirmation assay in the simultaneous urine drug testing and quantification of amphetamines, ketamines, and opiates. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:133 / 141
页数:9
相关论文
共 24 条
[1]   Interference by venlafaxine ingestion in the detection of tramadol by liquid chromatography linked to tandem mass spectrometry for the screening of illicit drugs in human urine [J].
Allen, KR .
CLINICAL TOXICOLOGY, 2006, 44 (02) :147-153
[2]  
[Anonymous], FED REG, V69, P19644
[3]  
[Anonymous], TD2010DCR WADA
[4]  
[Anonymous], 2011, STAT TABL UR DRUG TE
[5]  
[Anonymous], 2003, GUID IND MASS SPECTR
[6]  
Bland JM, 1999, STAT METHODS MED RES, V8, P135, DOI 10.1177/096228029900800204
[7]   Determination of illicit drugs and their metabolites in human urine by liquid chromatography tandem mass spectrometry including relative ion intensity criterion [J].
Concheiro, Marta ;
De Castro, Ana ;
Quintela, Oscar ;
Cruz, Angelines ;
Lopez-Rivadulla, Manuel .
JOURNAL OF ANALYTICAL TOXICOLOGY, 2007, 31 (09) :573-580
[8]   Online extraction LC-MS/MS method for the simultaneous quantitative confirmation of urine drugs of abuse and metabolites: Amphetamines, opiates, cocaine, cannabis, benzodiazepines and methadone [J].
de Jager, Andrew D. ;
Bailey, Neville L. .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2011, 879 (25) :2642-2652
[9]   Characteristics of superficially-porous silica particles for fast HPLC:: Some performance comparisons with sub-2-μm particles [J].
DeStefano, J. J. ;
Langlois, T. J. ;
Kirkland, J. J. .
JOURNAL OF CHROMATOGRAPHIC SCIENCE, 2008, 46 (03) :254-260
[10]   Simultaneous determination of multiple drugs of abuse and relevant metabolites in urine by LC-MS-MS [J].
Feng, June ;
Wang, Lanqing ;
Dai, Ingrid ;
Harmon, Tia ;
Bernert, John T. .
JOURNAL OF ANALYTICAL TOXICOLOGY, 2007, 31 (07) :359-368