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LC-MS/MS 法检测和确证人发中 21 种苯二氮䓬类药物和 3 种“Z 类药物”。

Detection and validated quantification of 21 benzodiazepines and 3 "z-drugs" in human hair by LC-MS/MS.

机构信息

Institute of Legal Medicine, University of Zurich, 8057 Zurich, Switzerland.

出版信息

Forensic Sci Int. 2012 Feb 10;215(1-3):64-72. doi: 10.1016/j.forsciint.2011.07.052. Epub 2011 Aug 27.

Abstract

A method for detection and quantification of 21 benzodiazepines and the pharmacologically related "z-drugs" in human hair samples was developed and fully validated using liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS). After methanolic and methanolic/aqueous extraction, the analytes were separated using two different LC-MS systems (AB Sciex 3200 QTRAP and AB Sciex 5500 QTRAP). Separation columns, mobile phases and MS modes for both systems were: Phenomenex Kinetex, 2.6 μm, 50/2.1; 5mM ammonium formate buffer pH 3.5/methanol, total flow 0.75 mL/min; electrospray ionization (ESI), multiple reaction monitoring (MRM), information dependent acquisition (IDA), enhanced product ion scan (EPI). The assays were found to be selective for the tested compounds (alprazolam, 7-aminoclonazepam, 7-aminoflunitrazepam, bromazepam, chlordiazepoxide, clonazepam, N-desalkylflurazepam, diazepam, flunitrazepam, flurazepam, alpha-hydroxymidazolam, lorazepam, lormetazepam, midazolam, nitrazepam, nordazepam, oxazepam, phenazepam, prazepam, temazepam, triazolam, zaleplon, zolpidem and zopiclone), all validation criteria were in the required ranges according to international guidelines, except for bromazepam. Matrix effects, and process efficiencies were in the acceptable ranges evaluated using the post-extraction addition approach. Lower limits of quantification were between 0.6 and 16 pg/mg of hair. The LC-MS/MS assay has proven to be applicable for determination of the studied analytes in human hair in numerous authentic cases (n=175).

摘要

建立并充分验证了一种使用液相色谱-串联质谱法(LC-MS/MS)检测和定量人发样品中 21 种苯并二氮䓬类药物和相关的“Z 药物”的方法。在甲醇和甲醇/水提取后,使用两种不同的 LC-MS 系统(AB Sciex 3200 QTRAP 和 AB Sciex 5500 QTRAP)分离分析物。两种系统的分离柱、流动相和 MS 模式为: Phenomenex Kinetex,2.6 μm,50/2.1;5mM 甲酸铵缓冲液 pH 3.5/甲醇,总流速 0.75 mL/min;电喷雾电离(ESI)、多反应监测(MRM)、信息相关采集(IDA)、增强子离子扫描(EPI)。结果表明,该方法对测试化合物(阿普唑仑、7-氨基氯硝西泮、7-氨基氟硝西泮、溴西泮、地西泮、氯硝西泮、N-去甲氟西泮、安定、氟硝西泮、氟西泮、α-羟咪达唑仑、劳拉西泮、劳拉西泮、咪达唑仑、硝西泮、去甲西泮、奥沙西泮、苯并二氮䓬、普拉西泮、替马西泮、三唑仑、扎来普隆、唑吡坦和佐匹克隆)具有选择性,除溴西泮外,所有验证标准均符合国际指南要求的范围内。使用提取后添加方法评估,基质效应和处理效率均在可接受范围内。定量下限在 0.6 到 16 pg/mg 头发之间。LC-MS/MS 测定法已被证明可应用于在许多真实案例(n=175)中测定人发中研究分析物。

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