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使用液相色谱-串联质谱法同时分析血液中的四氢大麻酚(THC)及其代谢物。

Simultaneous analysis of THC and its metabolites in blood using liquid chromatography-tandem mass spectrometry.

作者信息

Del Mar Ramirez Fernandez Maria, De Boeck Gert, Wood Michelle, Lopez-Rivadulla Manuel, Samyn Nele

机构信息

Federal Public Service Justice, National Institute of Criminalistics and Criminology, Chaussée de Vilvorde 100, 1120 Brussels, Belgium.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Nov 15;875(2):465-70. doi: 10.1016/j.jchromb.2008.09.032. Epub 2008 Oct 2.

Abstract

Cannabis is considered to be the most widely abused illicit drug in Europe. Consequently, sensitive and specific analytical methods are needed for forensic purposes and for cannabinoid pharmacokinetic and pharmacodynamic studies. A simple, rapid and highly sensitive and specific method for the extraction and quantification of Delta(9)-tetrahydrocannabinol (THC), 11-hydroxy- Delta(9)-tetrahydrocannabinol (11-OH-THC) and 11-nor-9-carboxy- Delta(9)-tetrahydrocannabinol (THC-COOH) in blood is presented. The method was fully validated according to international guidelines and comprises simultaneous liquid-liquid extraction (LLE) of the three analytes with hexane:ethyl acetate (90:10, v/v) into a single eluant followed by separation and quantification using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Chromatographic separation was achieved using a XBridge C(18) column eluted isocratically with methanol:0.1% formic acid (80:20, v/v). Selectivity of the method was achieved by a combination of retention time, and two precursor-product ion transitions. The use of the LLE was demonstrated to be highly effective and led to significant decreases in the interferences present in the matrix. Validation of the method was performed using 250 microL of blood. The method was linear over the range investigated (0.5-40 microg/L for THC, 1-40 microg/L for 11-OH-THC, and 2-160 microg/L for THC-COOH) with excellent intra-assay and inter-assay precision; relative standard deviations (RSDs) were <12% for THC and 11-OH-THC and <8% for THC-COOH for certified quality control samples. The lower limit of quantification was fixed at the lowest calibrator in the linearity experiments. No instability was observed after repeated freezing and thawing or in processed samples. The method was subsequently applied to 63 authentic blood samples obtained from toxicology cases. The validation and actual sample analysis results show that this method is rugged, precise, accurate, and well suited for routine analysis.

摘要

大麻被认为是欧洲滥用最为广泛的非法药物。因此,出于法医鉴定目的以及大麻素药代动力学和药效学研究的需要,必须要有灵敏且特异的分析方法。本文介绍了一种简单、快速、高度灵敏且特异的方法,用于血液中Δ⁹-四氢大麻酚(THC)、11-羟基-Δ⁹-四氢大麻酚(11-OH-THC)和11-去甲-9-羧基-Δ⁹-四氢大麻酚(THC-COOH)的提取和定量分析。该方法依据国际指南进行了全面验证,包括同时用己烷:乙酸乙酯(90:10,v/v)对三种分析物进行液液萃取(LLE),萃取至单一洗脱液中,随后使用液相色谱-串联质谱(LC-MS/MS)进行分离和定量分析。使用XBridge C₁₈柱,以甲醇:0.1%甲酸(80:20,v/v)等度洗脱实现色谱分离。该方法的选择性通过保留时间以及两个前体-产物离子转换相结合来实现。结果表明,液液萃取非常有效,可显著减少基质中存在的干扰。使用250微升血液对该方法进行验证。在所研究的范围内(THC为0.5 - 40微克/升,11-OH-THC为1 - 40微克/升,THC-COOH为2 - 160微克/升)该方法呈线性,批内和批间精密度良好;经认证的质量控制样品中,THC和11-OH-THC的相对标准偏差(RSD)<12%,THC-COOH的相对标准偏差<8%。定量下限确定为线性实验中最低的校准物。反复冻融或处理后的样品均未观察到不稳定性。该方法随后应用于从毒理学案例中获取的63份真实血液样本。验证和实际样品分析结果表明,该方法耐用、精密、准确,非常适合常规分析。

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