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快速气相色谱法和负离子化学电离串联质谱法用于全血中大麻素的法医分析。

Fast gas chromatography and negative-ion chemical ionization tandem mass spectrometry for forensic analysis of cannabinoids in whole blood.

作者信息

Thomas Aurélien, Widmer Christèle, Hopfgartner Gérard, Staub Christian

机构信息

Institute of Forensic Medicine, University of Geneva, Avenue de Champel 9, 1211 Geneva 4, Switzerland.

出版信息

J Pharm Biomed Anal. 2007 Nov 5;45(3):495-503. doi: 10.1016/j.jpba.2007.08.019. Epub 2007 Aug 23.

Abstract

The present work describes a fast gas chromatography/negative-ion chemical ionization tandem mass spectrometric assay (Fast GC/NICI-MS/MS) for analysis of tetrahydrocannabinol (THC), 11-hydroxy-tetrahydrocannabinol (THC-OH) and 11-nor-9-carboxy-tetrahydrocannabinol (THC-COOH) in whole blood. The cannabinoids were extracted from 500 microL of whole blood by a simple liquid-liquid extraction (LLE) and then derivatized by using trifluoroacetic anhydride (TFAA) and hexafluoro-2-propanol (HFIP) as fluorinated agents. Mass spectrometric detection of the analytes was performed in the selected reaction-monitoring mode on a triple quadrupole instrument after negative-ion chemical ionization. The assay was found to be linear in the concentration range of 0.5-20 ng/mL for THC and THC-OH, and of 2.5-100 ng/mL for THC-COOH. Repeatability and intermediate precision were found less than 12% for all concentrations tested. Under standard chromatographic conditions, the run cycle time would have been 15 min. By using fast conditions of separation, the assay analysis time has been reduced to 5 min, without compromising the chromatographic resolution. Finally, a simple approach for estimating the uncertainty measurement is presented.

摘要

本研究描述了一种用于分析全血中四氢大麻酚(THC)、11-羟基-四氢大麻酚(THC-OH)和11-去甲-9-羧基-四氢大麻酚(THC-COOH)的快速气相色谱/负离子化学电离串联质谱分析法(快速GC/NICI-MS/MS)。通过简单的液-液萃取(LLE)从500微升全血中提取大麻素,然后使用三氟乙酸酐(TFAA)和六氟-2-丙醇(HFIP)作为氟化剂进行衍生化。在负离子化学电离后,在三重四极杆仪器上采用选择反应监测模式对分析物进行质谱检测。该分析方法在THC和THC-OH浓度范围为0.5 - 20 ng/mL、THC-COOH浓度范围为2.5 - 100 ng/mL时呈线性。对于所有测试浓度,重复性和中间精密度均小于12%。在标准色谱条件下,运行周期时间为15分钟。通过使用快速分离条件,分析时间已缩短至5分钟,而不影响色谱分辨率。最后,提出了一种估计测量不确定度的简单方法。

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