尿中六氢大麻酚代谢物的鉴定。

IF 1.1 4区 化学 Q4 PHYSICS, ATOMIC, MOLECULAR & CHEMICAL
European Journal of Mass Spectrometry Pub Date : 2023-10-01 Epub Date: 2023-09-14 DOI:10.1177/14690667231200139
Willi Schirmer, Volker Auwärter, Julia Kaudewitz, Stefan Schürch, Wolfgang Weinmann
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引用次数: 1

摘要

六氢大麻酚(HHC)是一种大麻素,自1940年以来就被发现,但直到最近才被发现作为一种精神活性药物用于娱乐用途。在许多国家,HHC被用作四氢大麻酚(THC)的合法替代品,但最初的国家已经将其纳入麻醉药品法。我们的目的是评估一种可靠的分析方法,以LC-MS/MS和GC-MS证明HHC消耗。我们鉴定了两名志愿者(使用蒸发器吸入和口服)摄入HHC后的两种HHC外显子及其代谢物。使用文献数据(衍生物的EI-MS光谱)和参考化合物(只要是市售的)的LC-HR-MS/MS、LC-MS/MS和GC-MS进行代谢物鉴定。采用LC-HR-MS/MS和LC-MS/MS检测尿样中HHC和OH-HHC的ii相代谢物(葡萄糖醛酸盐)。GC-MS初步鉴定其主要代谢物为4'OH-HHC (C9和C4'的立体化学未知)。LC-MS/MS发现的另一个主要侧链羟基化代谢物无法明确鉴定。在尿液中发现了相当数量的11-OH-HHC的两个外显体。(8R, 9R)-8-OH-HHC经GC-MS和LC-MS/MS鉴定为微量代谢物。而(9S)-HHC在口服和吸入HHC后的尿液中发现,更有精神活性的外显体(9R)-HHC只在吸入后的尿液中发现。其他几个次要代谢物也被检测到,但没有结构鉴定。我们发现口服或吸入的非对映异构体混合HHC的尿液主要代谢物不同于各自的主要Δ9-THC代谢物(11-OH-Δ9-THC和11-不-9-羧基-Δ9-THC)。虽然建立了灵敏的LC-MS/MS和GC-SIM-MS方法检测对照化合物(9R)-11-no -9-carboxy- hhc和(9S)-11-no -9-carboxy- hhc,但这些氧化产物未在尿液中检测到。为了进一步提高灵敏度,建立了GC-MS/MS方法,确认HHC的11-no -9-羧基代谢物作为次要代谢物存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of human hexahydrocannabinol metabolites in urine.

Hexahydrocannabinol (HHC) is a cannabinoid that has been known since 1940 but has only recently found its way into recreational use as a psychoactive drug. HHC has been used as a legal alternative to tetrahydrocannabinol (THC) in many countries, but first countries already placed it under their narcotic substances law. Our aim was to evaluate a reliable analytical method for the proof of HHC consumption by LC-MS/MS and GC-MS. We identified the two epimers of HHC and metabolites after HHC consumption by two volunteers (inhalation by use of a vaporizer and oral intake). LC-HR-MS/MS, LC-MS/MS and GC-MS with literature data (EI-MS spectra of derivatives) and reference compounds - as far as commercially available - were used for metabolite identification. Phase-II-metabolites (glucuronides) of HHC and OH-HHC were found in urine samples with LC-HR-MS/MS and LC-MS/MS. The main metabolite was tentatively identified with GC-MS as 4'OH-HHC (stereochemistry on C9 and C4' unknown). Another major side-chain hydroxylated metabolite found by LC-MS/MS could not be unambiguously identified. Both epimers of 11-OH-HHC were found in considerable amounts in urine. (8R, 9R)-8-OH-HHC was identified as a minor metabolite with GC-MS and LC-MS/MS. While (9S)-HHC was found in urine after oral intake and inhalation of HHC, the more psychoactive epimer (9R)-HHC was only found in urine after inhalation. Several other minor metabolites were detected but not structurally identified. We found that after oral or inhalative consumption the urinary main metabolites of a diastereomeric mixture of HHC are different from the respective, major Δ9-THC metabolites (11-OH-Δ9-THC and 11-nor-9-carboxy-Δ9-THC). Although a sensitive LC-MS/MS and GC-SIM-MS method were set-up for the reference compounds (9R)-11-nor-9-carboxy-HHC and (9S)-11-nor-9-carboxy-HHC, these oxidation products were not detected in urine with these techniques. To further increase sensitivity, a GC-MS/MS method was developed, and the 11-nor-9-carboxy metabolites of HHC were confirmed to be present as minor metabolites.

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来源期刊
CiteScore
2.40
自引率
7.70%
发文量
16
审稿时长
>12 weeks
期刊介绍: JMS - European Journal of Mass Spectrometry, is a peer-reviewed journal, devoted to the publication of innovative research in mass spectrometry. Articles in the journal come from proteomics, metabolomics, petroleomics and other areas developing under the umbrella of the “omic revolution”.
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