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A validated workflow for drug detection in oral fluid by non-targeted liquid chromatography-tandem mass spectrometry

机译:经验证的非靶向液相色谱-串联质谱法检测口腔液中的药物的工作流程

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摘要

Oral fluid is recognized as an important specimen for drug testing. Common applications are monitoring in substance abuse treatment programs, therapeutic drug monitoring, pain management, workplace drug testing, clinical toxicology, and driving under the influence of drugs (DRUID). In this study, we demonstrate that non-targeted LC-MS/MS with subsequent compound identification by tandem mass spectral library search is a valuable tool for comprehensive detection and confirmation of drugs in oral fluid samples. The workflow developed involves solid-phase extraction and chromatographic separation on reversed phase materials. Mass spectrometric detection is accomplished on a quadrupole–quadrupole-time-of-flight instrument operated with data-dependent acquisition control. The workflow was optimized for 500 μl of neat oral fluid collected with the Greiner Bio-One saliva collection system. The fitness of the developed method was tested and proven by analyzing blank and spiked samples as well as 59 authentic patient samples. We could demonstrate that compounds with logP values in the range 0.5–5.5 are efficiently detected at low nanograms per milliliter concentrations. The true positive and true negative rates of automated library search were equal or close to 100%. The beauty of the non-targeted LC-MS/MS approach is the ability to detect compounds hardly included in routinely applied targeted assays, and this was demonstrated by detecting the synthetic opioid U-47700 in two patient samples. >Graphical abstract
机译:口服液被认为是药物测试的重要标本。常见的应用是药物滥用治疗计划中的监视,药物治疗监视,疼痛管理,工作场所药物测试,临床毒理学以及在药物影响下驾驶(DRUID)。在这项研究中,我们证明了非靶向LC-MS / MS和随后通过串联质谱库检索进行化合物鉴定是全面检测和确认口腔液样品中药物的有价值的工具。开发的工作流程涉及固相萃取和反相材料的色谱分离。质谱检测是在四极杆-四极杆飞行时间仪器上进行的,该仪器具有依赖于数据的采集控制。该工作流程针对使用Greiner Bio-One唾液收集系统收集的500μl纯净口腔液进行了优化。通过分析空白和加标样品以及59个真实的患者样品,测试并证明了所开发方法的适用性。我们可以证明logP值在0.5-5.5范围内的化合物可以在低纳克每毫升浓度下有效检测。自动化图书馆搜索的真实阳性率和真实阴性率等于或接近100%。非靶向LC-MS / MS方法的优点是能够检测常规应用的靶向测定法中几乎不包含的化合物,这通过在两个患者样品中检测到合成阿片类药物U-47700得以证明。 <!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> >图形摘要<!- fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> <!-标题a7->ᅟ

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