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采用分子印迹固相萃取-气相色谱-质谱法同时测定尿液中Δ9-四氢大麻酚及其主要代谢物

Molecularly imprinted solid phase extraction for simultaneous determination of Δ9-tetrahydrocannabinol and its main metabolites by gas chromatography-mass spectrometry in urine samples.

机构信息

Department of Forensic Medicine and Criminology, School of Medicine, University of Zagreb, Šalata 11, 10000 Zagreb, Croatia.

出版信息

Forensic Sci Int. 2013 Sep 10;231(1-3):317-24. doi: 10.1016/j.forsciint.2013.06.009. Epub 2013 Jul 9.

DOI:10.1016/j.forsciint.2013.06.009
PMID:23890655
Abstract

In presented paper analytical method based on solid-phase extraction using molecularly imprinted polymer and gas chromatography-mass spectrometry has been developed and validated for the confirmation of THC, THC-OH and THC-COOH in urine samples. Non-covalent molecularly imprinted polymers of THC-OH were prepared using different functional monomers (methacrylic acid, 4-vinylpyridine, and 2-hydroxyethyl methacrylate), ethylene glycol dimethacrylate as a cross-linker and 2,2'-azobis-isobutyronitrile as an initiator of radical polymerization. Analytes were extracted from urine samples using prepared polymer sorbent with highest binding selectivity and capability. Before extraction, urine samples were hydrolyzed with alkaline. Elution was performed with chloroform:ethyl acetate (60:40, v/v). Dry extracts were silylated with BSTFA+1% TMCS. Detection and quantification were performed using gas chromatography-mass spectrometry in single ion recording mode. The developed method was linear over the range from LOQ to 150 ng mL(-1) for all three analytes. For THC, THC-OH and THC-COOH LOD was 2.5, 1 and 1 ng mL(-1), and LOQ was 3, 2 and 2 ng mL(-1), respectively. The precision, accuracy, recovery and matrix effect were investigated at 5, 25 and 50 ng mL(-1). In the investigated concentration range recoveries were 71.9% for THC, 78.6% for THC-OH and 75.2% for THC-COOH. Matrix effect was not significant (<10%) for all analytes in the concentration range from 5 ng mL(-1) to 50 ng mL(-1). Extraction recovery on non-imprinted polymer was relatively high indicating high non-specific binding. Optimized and validated method was applied to 15 post-mortem urine samples.

摘要

本文介绍了一种基于固相萃取-分子印迹聚合物和气相色谱-质谱联用技术的分析方法,用于确证尿液中 THC、THC-OH 和 THC-COOH。采用不同的功能单体(甲基丙烯酸、4-乙烯吡啶和 2-羟乙基甲基丙烯酸酯)、乙二醇二甲基丙烯酸酯作为交联剂和 2,2'-偶氮二异丁腈作为自由基聚合引发剂,制备了 THC-OH 的非共价分子印迹聚合物。分析物用具有最高结合选择性和能力的聚合物吸附剂从尿液样品中提取。萃取前,尿液样品用碱性水解。用氯仿:乙酸乙酯(60:40,v/v)洗脱。干燥提取物用 BSTFA+1%TMCS 硅烷化。采用气相色谱-质谱单离子记录模式进行检测和定量。该方法在所有三种分析物的 LOQ 至 150ngmL(-1)范围内呈线性。对于 THC、THC-OH 和 THC-COOH,LOD 分别为 2.5、1 和 1ngmL(-1),LOQ 分别为 3、2 和 2ngmL(-1)。在 5、25 和 50ngmL(-1) 时,考察了精密度、准确度、回收率和基质效应。在所研究的浓度范围内,THC 的回收率为 71.9%,THC-OH 为 78.6%,THC-COOH 为 75.2%。在 5ngmL(-1)至 50ngmL(-1)的浓度范围内,所有分析物的基质效应均不显著(<10%)。非印迹聚合物的提取回收率相对较高,表明非特异性结合较高。优化和验证后的方法应用于 15 份死后尿液样本。

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