Sensitive gas chromatographic-mass spectrometric screening of acetylated benzodiazepines

被引:42
作者
Borrey, D
Meyer, E
Lambert, W
Van Calenbergh, S
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
[3] State Univ Ghent, Med Chem Lab, B-9000 Ghent, Belgium
关键词
derivatization; GC; pharmaceutical analysis; benzodiazepines;
D O I
10.1016/S0021-9673(00)01177-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
GC-MS screening conditions were developed for 15 low-dosed benzodiazepines, covering alprazolam, flunitrazepam, flurazepam, ketazolam, lorazepam and triazolam, and the corresponding metabolites alpha -hydroxyalprazolam, 4-hydroxy-alprazolam; 7-aminoflunitrazepam, desmethylflunitrazepam, 7-aminodesmethylflunitrazepam; hydroxyethylflurazepam, N-desalkylflurazepam; oxazepam and alpha -hydroxytriazolam, respectively. Benzodiazepines are analyzed on a polydimethylsiloxane column in both the scan and the multiple ion monitoring modes using on-column injection to attain maximal sensitivity. The reactive compounds are acetylated with pyridine and acetic anhydride for 20 min. The derivatives are stable for at least 4 days. The relative standard deviation observed with standard compounds at the low nanogram-level ranged from 1.13 to 4.87% within-day and from 1.12 to 4.94% between-day. Unequivocal identification potential, high chromatographic resolution and sensitivity are combined with minimal thermal degradation. The presented screening conditions provide the basis for a unique routine screening method for low-dosed benzodiazepines with a broad polarity range. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:105 / 118
页数:14
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