血液和尿液中四氢大麻酚异构体、类似物、同源物和代谢物的LC-MS/MS综合分析。

IF 2.3 3区 医学 Q3 CHEMISTRY, ANALYTICAL
Luette S Muir, Sarah E Doumit, Joshua Z Seither, Jessica L Knittel, Jeffrey P Walterscheid, Erin L Karschner
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引用次数: 0

摘要

大麻的合法化和以大麻为基础的提取物的商业化导致许多大麻素出现在消费品中。虽然缺乏delta-9-四氢大麻酚(∆9-THC)的许多同分异构体、类似物和同源物的人体药理数据,但这些大麻素可能能够诱导大麻模拟效应。由于重叠的保留时间和用于区分各种母体药物和代谢物的离子转移,结构相似性也构成了独特的分析挑战。因此,传统的含有Δ9-THC、11-羟基-Δ9-THC (11-OH-Δ9-THC)和11-不-9-羧基-Δ9-THC (Δ9-THCCOOH)的大麻素检测方法已不足以应对这种对公共安全的新威胁。已经开发并验证了一种新的方法,用于定量确认血液中的Δ8-和Δ9-THC,它们的羟基化和羧化代谢物,以及9(R)-和9(S)-六氢大麻酚(HHC)立体异构体,并定性鉴定尿液中的这些分析物。该方法还能定性确认∆9,11-THC (exo-THC), HHC和Δ6a,1°a-THC /Δ1°-THC羧化代谢物,以及Δ8和Δ9 THC同源物包括四氢大麻素(THCV),其代谢物11-非羧基THCV,四氢大麻酚(THCB),四氢大麻己醇(THCH;血液和尿液中的四氢大麻酚(THCP), THC-C8以及9(R)和9(S)-六氢大麻酚(HHCP)。非羧化分析物的检出限为1 ng/mL,羧化分析物的检出限为5 ng/mL。四氢大麻酚亲本、羟化异构体和HHC立体异构体的校准曲线在1 ~ 50 ng/mL范围内建立,羧化四氢大麻酚异构体的校准曲线在5 ~ 250 ng/mL范围内建立。该方法将所有感兴趣的分析物从潜在的合成副产物中分离出来,如∆8-iso-THC、∆4(8)-iso-THC和exo-THC。明确识别这些大麻素将提高法医毒理学报告的准确性,同时引导大麻监管和产品配方不断变化的环境。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive LC-MS-MS analysis of THC isomers, analogs, homologs, and metabolites in blood and urine.

The legalization of hemp and the commercialization of hemp-based extracts have resulted in numerous cannabinoids appearing in consumer products. Although human pharmacological data are lacking for many of these isomers, analogs, and homologs of delta-9-tetrahydrocannabinol (Δ9-THC), these cannabinoids may be capable of inducing cannabimimetic effects. Structural similarities also pose unique analytical challenges due to overlapping retention times and ion transitions used to distinguish between various parent drugs and metabolites. Therefore, traditional cannabinoid assays containing Δ9-THC, 11-hydroxy-Δ9-THC (11-OH-Δ9-THC), and 11-nor-9-carboxy-Δ9-THC (Δ9-THCCOOH) are no longer sufficient to confront this new threat to public safety. A new method has been developed and validated to quantitatively confirm Δ8- and Δ9-THC, their hydroxylated and carboxylated metabolites, and 9(R)- and 9(S)-hexahydrocannabinol (HHC) stereoisomers in blood and qualitatively identify these analytes in urine. This method is also capable of qualitatively confirming Δ9,11-THC (exo-THC), HHCCOOH, Δ6a,10a-THCCOOH/Δ10-THCCOOH, and Δ8 and Δ9 THC homologs including tetrahydrocannabivarin (THCV), tetrahydrocannabutol (THCB), tetrahydrocannabihexol (THCH; Δ8-THCH in urine only), tetrahydrocannabiphorol (THCP), THC-C8, as well as 9(R)- and 9(S)-hexahydrocannabiphorol (HHCP) in blood and urine. Limits of detection were 1 ng/mL for non-carboxylated analytes and 5 ng/mL for carboxylated analytes. Calibration curves for parent and hydroxylated THC isomers and HHC stereoisomers were 1 to 50 ng/mL, whereas calibration curves for the carboxylated THC isomers were 5-250 ng/mL. This method separates all analytes of interest from potential synthesis byproducts such as Δ8-iso-THC, Δ4(8)-iso-THC, and exo-THC. Unambiguous identification of these cannabinoids will increase forensic toxicology reporting accuracy while navigating the changing landscape of cannabis regulation and product formulation.

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来源期刊
CiteScore
5.10
自引率
20.00%
发文量
92
审稿时长
6-12 weeks
期刊介绍: The Journal of Analytical Toxicology (JAT) is an international toxicology journal devoted to the timely dissemination of scientific communications concerning potentially toxic substances and drug identification, isolation, and quantitation. Since its inception in 1977, the Journal of Analytical Toxicology has striven to present state-of-the-art techniques used in toxicology labs. The peer-review process provided by the distinguished members of the Editorial Advisory Board ensures the high-quality and integrity of articles published in the Journal of Analytical Toxicology. Timely presentation of the latest toxicology developments is ensured through Technical Notes, Case Reports, and Letters to the Editor.
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