Roche Diagnostics GmbH, Penzberg, Germany.
Drug Test Anal. 2012 Jul-Aug;4(7-8):668-74. doi: 10.1002/dta.1334. Epub 2012 Feb 28.
A fast and sensitive reference method for quantification of Δ(9) -tetrahydrocannabinol (THC) and its main metabolite 11-nor-9-carboxy-Δ(9) -tetrahydrocannabinol (THCCOOH) in oral fluid is described in this study. Samples were collected using an oral specimen collection device, followed by solid-phase extraction and liquid chromatography-tandem mass spectrometry analysis. Chromatographic separation of the analytes was achieved by gradient elution on a reversed-phase column with subsequent detection by electrospray triple quadrupole mass spectrometry in positive ionization multiple reaction monitoring mode. Quantification was performed by means of deuterated analogues of the analytes as internal standards. Total run time of the assay was 12 min. The method allowed sensitive quantification of both analytes at a limit of quantification of 0.2 ng/ml. This sensitivity is essential for analysis of samples collected with the Intercept Oral Fluid Collection device (OraSure) and an assay for simultaneous quantification of THC and THCCOOH in saliva has not yet been described. The calibration curves for THC and THCCOOH were linear in the range between 0.25 and 8 ng/ml (r(2) > 0.99). Ion suppression effects from endogenous or exogenous interferences were investigated using selected model substances (albumin, ascorbic acid, bilirubin, hemoglobin, breath spray, cigarette, chewing gum, chewing tobacco, candy, tooth whitening, and Tums antacid). These substances were chosen because of the high probability of their presence in the collected samples. None of the 11 endogenous model interferences altered the accuracy of analysis, demonstrating good robustness of the method with respect to interferences in common hygiene products, medicine, tobacco and naturally occurring endogenous substances.
本研究描述了一种快速灵敏的检测唾液中Δ(9)-四氢大麻酚(THC)及其主要代谢物 11-去甲-9-羧基-Δ(9)-四氢大麻酚(THCCOOH)的参考方法。采用口腔标本采集装置采集样品,然后进行固相萃取和液相色谱-串联质谱分析。采用反相柱进行梯度洗脱,实现分析物的色谱分离,随后采用电喷雾三重四极杆质谱在正离子多反应监测模式下进行检测。通过分析物的氘代类似物作为内标进行定量。整个分析时间为 12 分钟。该方法允许在定量下限为 0.2ng/ml 的情况下对两种分析物进行灵敏定量。这一灵敏度对于使用 Intercept 口腔液采集装置(OraSure)采集的样品分析至关重要,目前尚未描述用于唾液中同时定量检测 THC 和 THCCOOH 的分析方法。THC 和 THCCOOH 的校准曲线在 0.25 至 8ng/ml 范围内呈线性(r(2) > 0.99)。使用选定的模型物质(白蛋白、抗坏血酸、胆红素、血红蛋白、口气喷雾、香烟、口香糖、嚼烟、糖果、牙齿美白和 Tums 抗酸剂)研究了内源性或外源性干扰物的离子抑制效应。选择这些物质是因为它们在采集的样品中存在的可能性很高。在 11 种内源性模型干扰物中,没有一种会改变分析的准确性,这表明该方法对常见卫生产品、药物、烟草和天然内源性物质的干扰具有良好的稳健性。