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Direct analysis in real time (DART) and solid-phase microextraction (SPME) transmission mode (TM): a suitable platform for analysis of prohibited substances in small volumes

机译:实时直接分析(DART)和固相微萃取(SPME)传输模式(TM):分析小体积违禁物质的合适平台

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The reliable and rapid detection of small molecules in challenging sample volumes is of growing interest within the scientific community. In this paper, we document the use of an ambient ionization mass spectrometric (AIMS) technique, DART, coupled with SPME-TM to quantify drugs of abuse in 15 and 25 μL samples of oral fluid (OF) and blood. Combining DART's high detection sensitivity with SPME's pre-concentrating capability allowed us to achieve very low detection limits, with limits of quantitation (LOQs) ranging between 0.5 and 10 ng mL?1 for OF and 2.5 and 25 ng mL?1 for blood. The tested validation points (3, 30, and 90 ng mL?1 for OF; 37.5 and 250 ng mL?1 for blood) provided satisfactory accuracy and repeatability. Additionally, nicotine signals were detected in an OF sample from a male-smoker. Our results demonstrate that DART-MS/MS coupled with SPME-TM can be used as a tool for rapid small-volume analysis.
机译:在具有挑战性的样品量中,可靠,快速地检测小分子在科学界引起了越来越多的关注。在本文中,我们记录了环境电离质谱(AIMS)技术DART与SPME-TM的结合使用,以量化15和25μL口腔液(OF)和血液样本中的滥用药物。 DART的高检测灵敏度与SPME的预浓缩能力相结合,使我们能够实现非常低的检测限,定量限(LOQ)介于OF的0.5至10 ng mL?1和血液的2.5至25 ng mL?1之间。经测试的验证点(OF分别为3、30和90 ng mL?1;血液为37.5和250 ng mL?1)提供了令人满意的准确性和可重复性。此外,在来自男性吸烟者的OF样本中检测到尼古丁信号。我们的结果表明,结合SPME-TM的DART-MS / MS可以用作快速小体积分析的工具。

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