Scheunemann A, Elsner K, Germerott T, Hess C, Röhrich J
Institute of Legal Medicine, University Medical Center of the Johannes Gutenberg University Mainz, Am Pulverturm 3, 55131 Mainz, Germany.
Institute of Legal Medicine, University Medical Center of the Johannes Gutenberg University Mainz, Am Pulverturm 3, 55131 Mainz, Germany.
J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Apr 1;1173:122685. doi: 10.1016/j.jchromb.2021.122685.
The potential therapeutic effects of various phytocannabinoids and the availability of multiple cannabis-based medicines make it desirable to have an analytical method that simultaneously quantifies a wide range of cannabinoids in blood, beyond delta-9-tetrahydrocannabinol and its metabolites. A liquid chromatography tandem mass spectrometry (LC-MS/MS) method for quantification of 18 phytocannabinoids and cannabinoid metabolites in serum was developed and validated. The method enables simultaneous detection of delta-9-tetrahydrocannabinol, cannabidiol, cannabinol, cannabigerol, cannabichromene, cannabicyclol, tetrahydrocannabivarin and cannabidivarin and their acidic precursors tetrahydocannabinolic acid A, cannabidiolic acid, cannabinolic acid, cannabigerolic acid, cannabichromenic acid, cannabicyclolic acid, tetrahydrocannabivarinic acid and cannabidivarinic acid as well as the delta-9-tetrahydrocannabinol metabolites 11-hydroxy-tetrahydrocannabinol and 11-nor-9-carboxy-tetrahydrocannabinol. Limits of detection ranged from 0.0004 to 1 ng/mL and limits of quantification ranged from 0.004 to 2 ng/mL. Calibration curves of all analytes were linear over the whole calibration range. Recovery rates of 52 to 86% were obtained for all analytes except for cannabicyclol (49%), 11-nor-9-carboxy-tetrahydrocannabinol (46%), cannabichromenic acid (44%) and cannabidivarinic acid (36%). Acceptable bias and precision data were demonstrated for all analytes. The method was successfully applied to 55 forensic serum samples, obtained from the Institute of Legal Medicine Mainz.
各种植物大麻素的潜在治疗效果以及多种基于大麻的药物的可得性,使得人们期望拥有一种分析方法,能够同时定量血液中除9-四氢大麻酚及其代谢物之外的多种大麻素。开发并验证了一种用于定量血清中18种植物大麻素和大麻素代谢物的液相色谱串联质谱(LC-MS/MS)方法。该方法能够同时检测9-四氢大麻酚、大麻二酚、大麻酚、大麻萜酚、大麻色烯、大麻二环醇、四氢大麻酚酸和大麻二酚酸及其酸性前体四氢大麻酚酸A、大麻二酚酸、大麻酚酸、大麻萜酚酸、大麻色烯酸、大麻二环醇酸、四氢大麻酚酸和大麻二酚酸,以及9-四氢大麻酚代谢物11-羟基-四氢大麻酚和11-去甲-9-羧基-四氢大麻酚。检测限范围为0.0004至1 ng/mL,定量限范围为0.004至2 ng/mL。所有分析物的校准曲线在整个校准范围内均呈线性。除大麻二环醇(49%)、11-去甲-9-羧基-四氢大麻酚(46%)、大麻色烯酸(44%)和大麻二酚酸(36%)外,所有分析物的回收率为52%至86%。所有分析物均显示出可接受的偏差和精密度数据。该方法成功应用于从美因茨法医学研究所获得的55份法医血清样本。