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采用 LC-QTOF-MS 对口服液中的芬太尼类似物进行定量分析。

Quantification of fentanyl analogs in oral fluid using LC-QTOF-MS.

机构信息

Department of Forensic Science, College of Criminal Justice, Sam Houston State University, Huntsville, TX, USA.

出版信息

J Forensic Sci. 2021 Sep;66(5):1871-1878. doi: 10.1111/1556-4029.14813. Epub 2021 Jul 20.

Abstract

Oral fluid is a valuable alternative matrix for forensic toxicologists due to ease of observed collection, limited biohazardous exposure, and indications of recent drug use. Limited information is available for fentanyl analog prevalence, interpretation, or analysis in oral fluid. With increasing numbers of fentanyl-related driving under the influence of drug (DUID) cases appearing in the United States, the development of detection methods is critical. The purpose of the present study was to develop and validate a quantitative method for fentanyl analogs in oral fluid (collected via Quantisal™) using liquid chromatography-quadrupole-time-of-flight-mass spectrometry (LC-QTOF-MS). Validation resulted in limits of detection and quantification ranging from 0.5 to 1 ng/mL. Established linear range was 1-100 ng/mL for all analytes, except acetyl fentanyl at 0.5-100 ng/mL (R  > 0.994). Within- and between-run precision and bias were considered acceptable with maximum values of ±15.2%CV and ±14.1%, respectively. Matrix effects exhibited ionization enhancement for all analytes with intensified enhancement at a low concentration (9.3-47.4%). No interferences or carryover was observed. Fentanyl analogs were stable in processed extracts stored in the autosampler (4 C) for 48h. The validated method was used to quantify fentanyl analogs in authentic oral fluid samples (n=17) from probationers/parolees. Fentanyl and 4-ANPP concentrations were 1.0-104.5 ng/mL and 1.2-5.7 ng/mL, respectively.

摘要

唾液是法医毒理学家的一种有价值的替代基质,因为其采集方便、生物危害性暴露有限,并能反映近期的药物使用情况。目前关于唾液中芬太尼类似物的流行情况、解释或分析的信息有限。随着美国越来越多的与芬太尼相关的毒品影响下驾驶(DUID)案件出现,开发检测方法至关重要。本研究旨在开发和验证一种使用液相色谱-四极杆飞行时间质谱(LC-QTOF-MS)检测唾液中芬太尼类似物的定量方法(通过 Quantisal™采集)。验证结果表明,检测限和定量限范围为 0.5-1ng/mL。所有分析物的建立线性范围为 1-100ng/mL,除乙酰芬太尼为 0.5-100ng/mL(R >0.994)。批内和批间精密度和偏差均在可接受范围内,最大值分别为±15.2%CV 和±14.1%。所有分析物的基质效应均表现出离子增强作用,低浓度时增强作用更为明显(9.3-47.4%)。未观察到干扰或交叉污染。在自动进样器中(4°C)处理后的提取液中,芬太尼类似物在 48 小时内稳定。该验证方法用于对来自缓刑犯/假释犯的 17 份真实唾液样本中的芬太尼类似物进行定量。芬太尼和 4-ANPP 的浓度分别为 1.0-104.5ng/mL 和 1.2-5.7ng/mL。

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