Simultaneous Quantification of Triazolam and its Metabolites in Human Urine by Liquid Chromatography-Tandem Mass Spectrometry

被引:3
|
作者
Pan, Ryh-Nan [2 ]
Hsiong, Cheng-Huei [1 ]
Huang, Pei-Wei [1 ]
Tsai, Wei-Shiuan [1 ]
Li, Wen-Yi [1 ]
Pao, Li-Heng [1 ]
机构
[1] Natl Def Med Ctr, Sch Pharm, Taipei 114, Taiwan
[2] Taiwan Police Coll, Dept Disaster Management, Taipei, Taiwan
关键词
SOLID-PHASE EXTRACTION; GAS-CHROMATOGRAPHY; ALPHA-HYDROXYTRIAZOLAM; PLASMA; BENZODIAZEPINES;
D O I
10.1093/anatox/35.3.170
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simple, simultaneous, sensitive and selective liquid chromatography-tandem mass spectrometry (LC-MS-MS) method for the determination of triazolam and its metabolites, α-hydroxytriazolam (α-OHTRZ) and 4-hydroxytriazolam (4-OHTRZ), in human urine was developed and validated. Triazolam-d4 was used as the internal standard (IS). This analysis was carried out on a Thermo® C18 column, and the mobile phase was composed of acetonitrile/H2O/formic acid (35:65:0.2, v/v/v). Detection was performed on a triple-quadrupole tandem MS using positive ion mode electrospray ionization, and quantification was performed by multiple reaction monitoring mode. The MS-MS ion transitions monitored were m/z 343.1 → 308.3, 359.0 → 331.0, 359.0 → 111.2, and 347.0 → 312.0 for triazolam, α-OHTRZ, 4-OHTRZ, and triazolam-d4, respectively. The lower limits of quantification of the analytical method were 0.5 ng/mL for triazolam, 5 ng/mL for α-OHTRZ, and 0.5 ng/mL for 4-OHTRZ. The within- and between-run precisions were less than 15%, and accuracy was -12.33% to 9.76%. The method was proved to be accurate and specific, and it was applied to a urinary excretion study of triazolam in healthy Chinese volunteers. © 2010 Publishing Technology.
引用
收藏
页码:170 / 175
页数:6
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