Jiang Fengli, Rao Yulan, Wang Rong, Johansen Sys Stybe, Ni Chunfang, Liang Chen, Zheng Shuiqing, Ye Haiying, Zhang Yurong
Department of Forensic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, P. R. China.
Shanghai Key Laboratory of Crime Scene Evidence, Shanghai Institute of Forensic Science, Shanghai, P. R. China.
J Sep Sci. 2016 May;39(10):1873-83. doi: 10.1002/jssc.201600107. Epub 2016 May 6.
A novel and simple online solid-phase extraction liquid chromatography-tandem mass spectrometry method was developed and validated for the simultaneous determination of diazepam and its five metabolites including nordazepam, oxazepam, temazepam, oxazepam glucuronide, and temazepam glucuronide in human oral fluid. Human oral fluid was obtained using the Salivette(®) collection device, and 100 μL of oral fluid samples were loaded onto HySphere Resin GP cartridge for extraction. Analytes were separated on a Waters Xterra C18 column and quantified by liquid chromatography with tandem mass spectrometry using the multiple reaction monitoring mode. The whole procedure was automatic, and the total run time was 21 min. The limit of detection was in the range of 0.05-0.1 ng/mL for all analytes. The linearity ranged from 0.25 to 250 ng/mL for oxazepam, and 0.1 to 100 ng/mL for the other five analytes. Intraday and interday precision for all analytes was 0.6-12.8 and 1.0-9.2%, respectively. Accuracy ranged from 95.6 to 114.7%. Method recoveries were in the range of 65.1-80.8%. This method was fully automated, simple, and sensitive. Authentic oral fluid samples collected from two volunteers after consuming a single oral dose of 10 mg diazepam were analyzed to demonstrate the applicability of this method.
建立了一种新颖、简便的在线固相萃取液相色谱-串联质谱法,并对其进行了验证,用于同时测定人唾液中地西泮及其5种代谢物,包括去甲地西泮、奥沙西泮、替马西泮、奥沙西泮葡萄糖醛酸苷和替马西泮葡萄糖醛酸苷。使用Salivette®采集装置获取人唾液,将100μL唾液样本加载到HySphere Resin GP柱上进行萃取。分析物在Waters Xterra C18柱上分离,采用多反应监测模式通过液相色谱-串联质谱法定量。整个过程是自动的,总运行时间为21分钟。所有分析物的检测限在0.05-0.1 ng/mL范围内。奥沙西泮的线性范围为0.25至250 ng/mL,其他5种分析物的线性范围为0.1至100 ng/mL。所有分析物的日内和日间精密度分别为0.6-12.8%和1.0-9.2%。准确度范围为95.6至114.7%。方法回收率在65.1-80.8%范围内。该方法完全自动化、简便且灵敏。分析了两名志愿者单次口服10 mg地西泮后采集的真实唾液样本,以证明该方法的适用性。