首页> 美国卫生研究院文献>Journal of Analytical Toxicology >Simultaneous GC–EI-MS Determination of Δ9-Tetrahydrocannabinol 11-Hydroxy-Δ9-Tetrahydrocannabinol and 11-nor-9-Carboxy-Δ9-Tetrahydrocannabinol in Human Urine Following Tandem Enzyme-Alkaline Hydrolysis
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Simultaneous GC–EI-MS Determination of Δ9-Tetrahydrocannabinol 11-Hydroxy-Δ9-Tetrahydrocannabinol and 11-nor-9-Carboxy-Δ9-Tetrahydrocannabinol in Human Urine Following Tandem Enzyme-Alkaline Hydrolysis

机译:串联酶-碱性水解后同时测定人尿中的Δ9-四氢大麻酚11-羟基-Δ9-四氢大麻酚和11-nor-9-羧基-Δ9-四氢大麻酚

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摘要

A sensitive and specific method for extraction and quantification of Δ9-tetrahydrocannabinol (THC), 11-hydroxy-Δ9-tetrahydrocannabinol (11-OH-THC), and 11-nor-9-carboxy-Δ9-tetrahydrocannabinol (THCCOOH) in human urine was developed and fully validated. To ensure complete hydrolysis of conjugates and capture of total analyte content, urine samples were hydrolyzed by two methods in series. Initial hydrolysis was with Escherichia coli β-glucuronidase (Type IX–A) followed by a second hydrolysis utilizing 10N NaOH. Specimens were adjusted to pH 5−6.5, treated with acetonitrile to precipitate protein, and centrifuged, and the supernatants were subjected to solid-phase extraction. Extracted analytes were derivatized with BSTFA and quantified by gas chromatography–mass spectrometry with electron impact ionization. Standard curves were linear from 2.5 to 300 ng/mL. Extraction efficiencies were 57.0−59.3% for THC, 68.3−75.5% for 11-OH-THC, and 71.5−79.7% for THCCOOH. Intra- and interassay precision across the linear range of the assay ranged from 0.1 to 4.3% and 2.6 to 7.4%, respectively. Accuracy was within 15% of target concentrations. This method was applied to the analysis of urine specimens collected from individuals participating in controlled administration cannabis studies, and it may be a useful analytical procedure for determining recency of cannabis use in forensic toxicology applications.
机译:灵敏,特异的提取和定量Δ 9 -四氢大麻酚(THC),11-羟基-Δ 9 -四氢大麻酚(11-OH-THC)和11的方法开发并充分验证了人类尿液中的-nor-9-羧基-Δ 9 -四氢大麻酚(THCCOOH)。为确保缀合物完全水解并捕获总分析物含量,尿液样品通过两种串联的方法进行水解。最初的水解过程是用大肠杆菌β-葡萄糖醛酸苷酶(IX-A型)进行,然后用10N NaOH进行第二次水解。将样品调节至pH 5-6.5,用乙腈处理以沉淀蛋白质,然后离心,然后将上清液进行固相萃取。提取的分析物用BSTFA衍生化,并通过带有电子碰撞电离的气相色谱-质谱法进行定量。标准曲线在2.5至300 ng / mL之间呈线性关系。 THC的萃取效率为57.0-59.3%,11-OH-THC的萃取效率为68.3-75.5%,THCCOOH的萃取效率为71.5-79.7%。整个测定线性范围内的测定内和测定间精密度分别为0.1%至4.3%和2.6%至7.4%。准确度在目标浓度的15%以内。该方法用于分析从参加受控管理大麻研究的个人收集的尿液样本,它可能是确定法医毒理学应用中大麻使用率的有用分析方法。

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