A Validated Screening and Confirmation Method for 946 Drugs and Metabolites Using LC-QTOF-MS with SWATH Acquisition.

IF 2.3 3区 医学 Q3 CHEMISTRY, ANALYTICAL
Maria Sarkisian, Luke N Rodda
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引用次数: 0

Abstract

A streamlined liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QTOF-MS) method utilizing protein precipitation and filtration extraction was developed to achieve rapid and reliable screening and confirmation for blood and urine matrices. This method targets 946 drugs and metabolites across 35 drug classes via sequential window acquisition of all theoretical mass spectra (SWATH) acquisition with variable customized windows to enhance spectral clarity, and was validated per established guidelines to ensure high accuracy and reproducibility. Combined with complementary in-house methods, this approach meets and exceeds the testing requirements outlined in ANSI/ASB standards and recommendations for postmortem, drug-facilitated crime (DFC) and Tier I and II driving under the influence of drug (DUID) analyses. The method demonstrated efficient and sensitive performance, achieving limits of detection as low as 0.1 ng/mL. It accurately identified expected detections across 67 proficiency test samples and 224 authentic case samples, with high accuracy and reliability in the detection of both traditional drugs and novel psychoactive substances (NPS). The method employs an in-house built library and incorporates in-batch standards analyzed alongside case samples to ensure contemporaneous identification criteria, making it suitable for confirmation and reporting purposes. By expanding the analytical capabilities to include a vast range of analytes, this method improves the likelihood of identifying substances that may otherwise go undetected, and reduces the need for multiple separate tests, thereby enhancing the overall effectiveness of toxicological investigations.

LC-QTOF-MS对946种药物及其代谢物的筛选和确认方法
建立了一种利用蛋白质沉淀和过滤萃取的流线型液相色谱四极杆飞行时间质谱(LC-QTOF-MS)方法,以实现血液和尿液基质的快速可靠筛选和确认。该方法针对35种药物类别中的946种药物和代谢物,通过所有理论质谱(SWATH)获取的顺序窗口获取,具有可变定制窗口,以提高光谱清晰度,并根据既定指南进行验证,以确保高精度和可重复性。结合互补的内部方法,这种方法满足并超过了ANSI/ASB标准和建议中关于死后、毒品促成的犯罪(DFC)和一级和二级毒品影响下驾驶(DUID)分析的测试要求。该方法高效灵敏,检出限低至0.1 ng/mL。它准确地确定了67个熟练程度测试样本和224个真实病例样本的预期检测,在检测传统药物和新型精神活性物质(NPS)方面都具有很高的准确性和可靠性。该方法采用内部建立的库,并结合与病例样本一起分析的批量标准,以确保同时识别标准,使其适合确认和报告目的。通过将分析能力扩大到包括广泛的分析物,该方法提高了识别可能未被发现的物质的可能性,并减少了多次单独测试的需要,从而提高了毒理学调查的总体有效性。
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来源期刊
CiteScore
5.10
自引率
20.00%
发文量
92
审稿时长
6-12 weeks
期刊介绍: The Journal of Analytical Toxicology (JAT) is an international toxicology journal devoted to the timely dissemination of scientific communications concerning potentially toxic substances and drug identification, isolation, and quantitation. Since its inception in 1977, the Journal of Analytical Toxicology has striven to present state-of-the-art techniques used in toxicology labs. The peer-review process provided by the distinguished members of the Editorial Advisory Board ensures the high-quality and integrity of articles published in the Journal of Analytical Toxicology. Timely presentation of the latest toxicology developments is ensured through Technical Notes, Case Reports, and Letters to the Editor.
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