LC-MS-MS quantification of Δ8-THC, Δ9-THC, THCV isomers and their main metabolites in human plasma.

IF 2.3 3区 医学 Q3 CHEMISTRY, ANALYTICAL
Cristina Sempio, Jorge Campos-Palomino, Jelena Klawitter, Amy Harrison, Erica N Peters, Laura MacNair, Mehdi Haghdoost, Marcel Bonn-Miller, Shanna Babalonis, Marilyn A Huestis, Uwe Christians, Jost Klawitter
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引用次数: 0

Abstract

In recent years, potential therapeutic applications of several different cannabinoids, such as Δ9-tetrahydrocannabinol (Δ9-THC), its isomer Δ8-THC and Δ9-tetrahydrocannabivarin (Δ9-THCV), have been investigated. Nevertheless, to establish dose-effect relationship and to gain knowledge of their pharmacokinetics and metabolism, sensitive and specific analytical assays are needed to measure these compounds in patients. For this reason, we developed and validated an online extraction high-performance liquid/liquid chromatography-tandem mass spectrometry (LC/LC-MS-MS) method for the simultaneous quantification of 13 cannabinoids and metabolites including the Δ8 and Δ9 isomers of THC, THCV and those of their major metabolites in human plasma. Plasma was fortified with cannabinoids at varying concentrations within the working range of the respective compound and 200 µL was extracted using a simple one-step protein precipitation procedure. The extracts were analyzed using online trapping LC/LC-atmospheric pressure chemical ionization-MS-MS running in the positive multiple reaction monitoring mode. The lower limit of quantification ranged from 0.5 to 2.5 ng/mL, and the upper limit of quantification was 400 ng/mL for all analytes. Inter-day analytical accuracy and imprecision ranged from 82.9% to 109% and 4.3% to 20.3% (coefficient of variance), respectively. Of 534 plasma samples following controlled oral administration of Δ8-THCV, 236 were positive for Δ8-THCV (median; interquartile ranges: 3.5 ng/mL; 1.8-11.9 ng/mL), 383 for the major metabolite (-)-11-nor-9-carboxy-Δ8-tetrahydrocannabivarin (Δ8-THCV-COOH) (95.4 ng/mL; 20.7-328 ng/mL), 260 for (-)-11-nor-9-carboxy-Δ9-tetrahydrocannabivarin (Δ9-THCV-COOH) (5.8 ng/mL; 2.5-16.1 ng/mL), 157 for (-)-11-hydroxy-Δ8-tetrahydrocannabivarin (11-OH-Δ8-THCV) (1.7 ng/mL; 1.0-3.7 ng/mL), 49 for Δ8-THC-COOH (1.7 ng/mL; 1.4-2.3 ng/mL) and 42 for Δ9-THCV (1.3 ng/mL; 0.8-1.6 ng/mL). We developed and validated the first LC/LC-MS-MS assay for the specific quantification of Δ8-THC, Δ9-THC and THCV isomers and their respective metabolites in human plasma. Δ8-THCV-COOH, 11-hydroxy-Δ8-THCV and Δ9-THCV-COOH were the major Δ8-THCV metabolites in human plasma after oral administration of 98.6% pure Δ8-THCV.

LC-MS/MS 定量分析人体血浆中的Δ8-THC、Δ9-THC、THCV ISOMERS 及其主要代谢物。
背景:近年来,人们研究了几种不同大麻素的潜在治疗用途,如Δ9-四氢大麻酚(Δ9-THC)、其异构体Δ8-THC 和Δ9-四氢大麻烷(Δ9-THCV)。然而,要建立剂量效应关系并了解它们的药代动力学和新陈代谢,还需要灵敏而特异的分析方法来测量患者体内的这些化合物。为此,我们开发并验证了一种在线萃取高效液相色谱-串联质谱(LC/LC-MS/MS)方法,用于同时定量检测人体血浆中的 13 种大麻素及其代谢物,包括 THC 的 Δ8 和 Δ9 异构体、THCV 及其主要代谢物:在血浆中添加相应化合物工作范围内不同浓度的大麻素,然后使用简单的一步式蛋白质沉淀法提取 200 µL 的血浆。提取物采用在线捕集液相色谱/液相色谱-大气压化学电离(APCI)-多反应监测(MRM)模式进行分析:所有分析物的定量下限为 0.5 至 2.5 纳克/毫升,定量上限为 400 纳克/毫升。日间分析的准确度和不精确度分别为 82.9%至 109%和 4.3%至 20.3%(方差系数)。在控制性口服 Δ8-THCV 后的 534 份血浆样本中,236 份对Δ8-THCV 呈阳性(中位数;四分位间范围:3.5 纳克/毫升;1.8 - 11.9 纳克/毫升),383 份对主要代谢物 (-)-11-nor-9-carboxy-Δ8-tetrahydrocannabivarin (Δ8-THCV-COOH) 呈阳性(95.4 纳克/毫升;20.7 - 328 ng/mL),(-)-11-去甲-9-羧基-Δ9-四氢大麻烷(Δ9-THCV-COOH)为 260(5.8 ng/mL;2.5 - 16.1 ng/mL),(-)-11-羟基-Δ8-四氢大麻烷(11-OH-Δ8-THCV)为 157(1.7纳克/毫升;1.0 - 3.7纳克/毫升),Δ8-THC-COOH为49纳克/毫升(1.7纳克/毫升;1.4 - 2.3纳克/毫升),Δ9-THCV为42纳克/毫升(1.3纳克/毫升;0.8 - 1.6纳克/毫升):我们开发并验证了首个用于特异性定量人体血浆中Δ8-THC、Δ9-THC 和 THCV 异构体及其各自代谢物的 LC/LC-MS/MS 检测方法。口服 98.6% 纯度的 Δ8-THCV 后,人体血浆中的Δ8-THCV-COOH、11-羟基-Δ8-THCV 和 Δ9-THCV-COOH 是主要的 Δ8-THCV 代谢物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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