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液相色谱-串联质谱法对口腔液中苯丙胺、阿片类药物、苯环利定、可卡因和苯甲酰爱康宁分析的验证

Validation of analysis of amphetamines, opiates, phencyclidine, cocaine, and benzoylecgonine in oral fluids by liquid chromatography-tandem mass spectrometry.

作者信息

Kala Subbarao V, Harris Steve E, Freijo Tom D, Gerlich Stan

机构信息

One Source Toxicology Laboratory, 1213 Genoa Red Bluff, Pasadena, Texas 77504, USA.

出版信息

J Anal Toxicol. 2008 Oct;32(8):605-11. doi: 10.1093/jat/32.8.605.

DOI:10.1093/jat/32.8.605
PMID:19007510
Abstract

The aim of the present study was to develop and validate a method for the detection and quantitation of drugs of abuse in oral fluids. Fortified oral fluid samples (made in-house) and samples from donors collected with Quantasil oral fluid collection kits from Immunalysis were screened on an Olympus 5400 using reagents purchased from Immunalysis. Amphetamines (AMPs), opiates, phencyclidine (PCP), and cocaine and its metabolite benzoylecgonine (BE) in oral fluids were quantitated by an Applied Biosystems 3200 QTRAP liquid chromatograph-tandem mass spectrometer (LC-MS-MS). AMPs, opiates, PCP, cocaine, and BE were extracted from samples using liquid-liquid or solid-phase extractions and the extracts were separated on a Shimadzu high-performance liquid chromatograph prior to the MS-MS analysis. For each drug, two multiple reaction mode transitions were monitored using positive electrospray ionization coupled to an MS-MS detector. Corresponding d3, d5, d6, and d11 internal standards were used to quantitate the results. The limit of detection/quantitation for AMPs, opiates, PCP, cocaine, and its metabolite BE were 10, 10, 2, 2, and 2 ng/mL of oral fluid, respectively, on a signal-to-noise ratio > 4. This corresponded to 25, 25, 5, 5, and 5 pg on column. The method was verified by participating in the North America Oral Fluid Proficiency Testing administered by Research Triangle Institute and by analyzing real samples from donors. In conclusion, LC-MS-MS provided a simple way to analyze and quantitate drugs of abuse in oral fluids.

摘要

本研究的目的是开发并验证一种检测和定量口腔液中滥用药物的方法。使用从Immunalysis购买的试剂,在Olympus 5400上对强化口腔液样本(自制)以及使用Immunalysis的Quantasil口腔液采集试剂盒从捐献者处收集的样本进行筛查。通过Applied Biosystems 3200 QTRAP液相色谱 - 串联质谱仪(LC-MS-MS)对口腔液中的苯丙胺类(AMPs)、阿片类、苯环己哌啶(PCP)、可卡因及其代谢物苯甲酰爱康宁(BE)进行定量。使用液 - 液萃取或固相萃取从样本中提取AMPs、阿片类、PCP、可卡因和BE,提取物在进行MS-MS分析之前在岛津高效液相色谱仪上进行分离。对于每种药物,使用正电喷雾电离与MS-MS检测器联用监测两个多反应模式转换。使用相应的d3、d5、d6和d11内标对结果进行定量。在信噪比> 4的情况下,AMPs、阿片类、PCP、可卡因及其代谢物BE在口腔液中的检测/定量限分别为10、10、2、2和2 ng/mL。这相当于柱上25、25、5、5和5 pg。通过参加由三角研究园研究所管理的北美口腔液能力验证测试以及分析来自捐献者的实际样本对该方法进行了验证。总之,LC-MS-MS提供了一种简单的方法来分析和定量口腔液中的滥用药物。

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