Simultaneous determination of fifteen low-dosed benzodiazepines in human urine by solid-phase extraction and gas chromatography-mass spectrometry

被引:62
作者
Borrey, D
Meyer, E
Lambert, W
Van Peteghem, C
De Leenheer, AP
机构
[1] State Univ Ghent, Toxicol Lab, B-9000 Ghent, Belgium
[2] State Univ Ghent, Lab Fysiol Biochem & Biometrie, B-9820 Merelbeke, Belgium
来源
JOURNAL OF CHROMATOGRAPHY B | 2001年 / 765卷 / 02期
关键词
benzodiazepines;
D O I
10.1016/S0378-4347(01)00419-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A gas chromatographic-mass spectrometric method was developed for the simultaneous analysis of 15 low-dosed benzodiazepines, both parent compounds and their corresponding metabolites, in human urine. The target compounds are alprazolam, alpha -hydroxyalprazolam, 4-hydroxyalprazolam, flunitrazepam, 7-aminoflunitrazepam, desmethylflunitrazepam, flurazepam, hydroxyethylflurazepam, nitrogen-desalkylflurazepam, ketazolam, oxazepam, lormetazepam, lorazepam, triazolam and alpha -hydroxytriazolam. Nitrogen-methylclonazepam is used as the internal standard. The urine sample preparation involves enzymatic hydrolysis of the conjugated metabolites with Helix pomatia beta -glucuronidase for 1 h at 56 degreesC followed by solid-phase extraction on a phenyl-type column. The extracted benzodiazepines are subsequently analyzed on a polydimethylsiloxane column using on-column injection to enhance sensitivity. The extraction efficiency exceeded 80% for all compounds except for oxazepam, lorazepam and 4-hydroxyalprazolam which had recoveries of about 60%. The LODs ranged from 13 to 30 ng/ml in the scan mode and from 1.0 to 1.7 ng/ml in the selected ion monitoring (SIM) mode. Linear calibration curves were obtained in the concentration ranges from 50 to 1000 ng/ml in the scan mode and from 5 to 100 ng/ml in the SLM mode. The within-day and day-to-day relative standard deviations at three different concentrations never exceeded 15%. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:187 / 197
页数:11
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