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首页> 外文期刊>Analytical and Bioanalytical Chemistry >11-Nor-9-carboxy-∆9-tetrahydrocannabinol quantification in human oral fluid by liquid chromatography–tandem mass spectrometry
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11-Nor-9-carboxy-∆9-tetrahydrocannabinol quantification in human oral fluid by liquid chromatography–tandem mass spectrometry

机译:液相色谱-串联质谱法测定人口腔液中的11-Nor-9-羧基-Δ9-四氢大麻酚

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摘要

Currently, ∆9-tetrahydrocannabinol (THC) is the analyte quantified for oral fluid cannabinoid monitoring. The potential for false-positive oral fluid cannabinoid results from passive exposure to THC-laden cannabis smoke raises concerns for this promising new monitoring technology. Oral fluid 11-nor-9-carboxy-∆9-tetrahydrocannabinol (THCCOOH) is proposed as a marker of cannabis intake since it is not present in cannabis smoke and was not measureable in oral fluid collected from subjects passively exposed to cannabis. THCCOOH concentrations are in the picogram per milliliter range in oral fluid and pose considerable analytical challenges. A liquid chromatography–tandem mass spectrometry (LCMSMS) method was developed and validated for quantifying THCCOOH in 1 mL Quantisal-collected oral fluid. After solid phase extraction, chromatography was performed on a Kinetex C18 column with a gradient of 0.01 % acetic acid in water and 0.01 % acetic acid in methanol with a 0.5-mL/min flow rate. THCCOOH was monitored in negative mode electrospray ionization and multiple reaction monitoring mass spectrometry. The THCCOOH linear range was 12–1,020 pg/mL (R 2 > 0.995). Mean extraction efficiencies and matrix effects evaluated at low and high quality control (QC) concentrations were 40.8–65.1 and −2.4–11.5 %, respectively (n = 10). Analytical recoveries (bias) and total imprecision at low, mid, and high QCs were 85.0–113.3 and 6.6–8.4 % coefficient of variation, respectively (n = 20). This is the first oral fluid THCCOOH LCMSMS triple quadrupole method not requiring derivatization to achieve a <15 pg/mL limit of quantification. The assay is applicable for the workplace, driving under the influence of drugs, drug treatment, and pain management testing.
机译:目前,∆9-四氢大麻酚(THC)是用于口服液大麻素监测的定量分析物。被动暴露于富含THC的大麻烟中可能导致假阳性口腔液大麻素的产生,引起人们对该新监测技术的关注。口服液11-去甲9-羧基-∆9-四氢大麻酚(THCCOOH)被认为是大麻摄入的标志物,因为它不存在于大麻烟雾中,并且在从被动接触大麻的受试者收集的口腔液中也无法测量。口服液中THCCOOH的浓度在每毫升皮克的范围内,对分析提出了很大挑战。液相色谱-串联质谱(LCMSMS)方法得到了开发并经过验证,可用于量化1 mL Quantisal收集的口腔液中的THCCOOH。固相萃取后,在Kinetex C18色谱柱上进行色谱分离,梯度为水中的0.01%乙酸和甲醇中的0.01%乙酸,流速为0.5mL / min。用负模式电喷雾电离和多反应监测质谱法监测THCCOOH。 THCCOOH线性范围为12–1,020 pg / mL(R 2> 0.995)。在低和高质量控制(QC)浓度下评估的平均提取效率和基质效应分别为40.8–65.1和-2.4–11.5%(n = 10)。低,中和高QC的分析回收率(bias)和总不准确度分别为85.0–113.3和6.6–8.4%变异系数(n = 20)。这是第一种无需衍生即可达到<15pg / mL定量限的THCCOOH LCMSMS三重四极杆口服液。该方法适用于工作场所,受药物,药物治疗和疼痛管理测试的影响。

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