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采用气相色谱-串联质谱法测定人血浆中的Δ-9-四氢大麻酚(THC)、11-羟基-THC、11-去甲-9-羧基-THC和大麻二酚

Determination of ∆-9-Tetrahydrocannabinol (THC), 11-hydroxy-THC, 11-nor-9-carboxy-THC and Cannabidiol in Human Plasma using Gas Chromatography-Tandem Mass Spectrometry.

作者信息

Andrenyak David M, Moody David E, Slawson Matthew H, O'Leary Daniel S, Haney Margaret

机构信息

Center for Human Toxicology, Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, UT, USA.

Department of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, IA, USA.

出版信息

J Anal Toxicol. 2017 May 1;41(4):277-288. doi: 10.1093/jat/bkw136.

Abstract

Two marijuana compounds of particular medical interest are delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD). A gas chromatography-tandem mass spectrometry (GC-MS-MS) method was developed to test for CBD, THC, hydroxy-THC (OH-THC) and carboxy-THC (COOH-THC) in human plasma. Calibrators (THC and OH-THC, 0.1 to 100; CBD, 0.25 to 100; COOH-THC, 0.5-500 ng/mL) and controls (0.3, 5 and 80 ng/mL, except COOH-THC at 1.5, 25 and 400 ng/mL) were prepared in blank matrix. Deuterated (d3) internal standards were added to 1-mL samples. Preparation involved acetonitrile precipitation, liquid-liquid extraction (hexane:ethyl acetate, 9:1), and MSTFA derivatization. An Agilent 7890 A GC was interfaced with an Agilent 7000 MS Triple Quadrupole. Selected reaction monitoring was employed. Blood samples were provided from a marijuana smoking study (two participants) and a CBD ingestion study (eight participants). Three analytes with the same transitions (THC, OH-THC and COOH-THC) were chromatographically separated. Matrix selectivity studies showed endogenous chromatographic peak area ratios (PAR) at the analyte retention times were <20% of the analyte limit of quantitation PAR. The intra-assay accuracy ranged from 83.5% to 118% of target and the intra-run imprecision ranged from 2.0% to 19.1%. The inter-assay accuracy ranged from 90.3% to 104% of target and the inter-run imprecision ranged from 6.5% to 12.0%. Stability was established for 25 hours at room temperature, 207 days at -20°C, after three freeze-thaw cycles and for 26 days for rederivatized processed samples. After smoking marijuana predictable concentrations of THC, OH-THC and COOH-THC were seen; low concentrations of CBD were detected at early time points. In moderate users who had not smoked for at least 9 hours before ingesting an 800 mg oral dose of CBD, the method was sensitive enough to follow residual concentrations of THC and OH-THC; sustained COOH-THC concentrations over 50 ng/mL validated its higher analytical range.

摘要

两种具有特殊医学意义的大麻化合物是Δ⁹ - 四氢大麻酚(THC)和大麻二酚(CBD)。开发了一种气相色谱 - 串联质谱(GC - MS - MS)方法来检测人血浆中的CBD、THC、羟基 - THC(OH - THC)和羧基 - THC(COOH - THC)。在空白基质中制备校准物(THC和OH - THC,0.1至100;CBD,0.25至100;COOH - THC,0.5 - 500 ng/mL)和对照品(0.3、5和80 ng/mL,COOH - THC除外,为1.5、25和400 ng/mL)。将氘代(d3)内标添加到1 - mL样品中。样品制备包括乙腈沉淀、液 - 液萃取(己烷:乙酸乙酯,9:1)和MSTFA衍生化。安捷伦7890 A气相色谱仪与安捷伦7000 MS三重四极杆联用。采用选择反应监测。血液样本来自一项大麻吸食研究(两名参与者)和一项CBD摄入研究(八名参与者)。三种具有相同跃迁的分析物(THC、OH - THC和COOH - THC)通过色谱法分离。基质选择性研究表明,在分析物保留时间处的内源性色谱峰面积比(PAR)小于分析物定量限PAR的20%。批内准确度在目标值的83.5%至118%之间,批内精密度在2.0%至19.1%之间。批间准确度在目标值的90.3%至104%之间,批间精密度在6.5%至12.0%之间。在室温下稳定性为25小时,在 - 20°C下为207天,经过三次冻融循环后以及衍生化处理后的样品为26天。吸食大麻后,可预测到THC、OH - THC和COOH - THC的浓度;在早期时间点检测到低浓度的CBD。在中度使用者中,他们在摄入800 mg口服剂量的CBD之前至少9小时未吸食大麻,该方法灵敏到足以追踪THC和OH - THC的残留浓度;持续的COOH - THC浓度超过50 ng/mL验证了其较高的分析范围。

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