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使用与差分离子迁移谱-质谱联用的3D打印开放式端口探头分析尿液样本中的非法药丸和滥用药物。

Analysis of illicit pills and drugs of abuse in urine samples using a 3D-printed open port probe hyphenated with differential mobility spectrometry-mass spectrometry.

作者信息

Sosnowski Piotr, Marin Victor, Tian Xiaobo, Hopfgartner Gérard

机构信息

Life Sciences Mass Spectrometry, Department of Inorganic and Analytical Chemistry, University of Geneva, Quai Ernest Ansermet 24, 1211, Geneva, Switzerland.

出版信息

Analyst. 2022 Sep 26;147(19):4318-4325. doi: 10.1039/d2an00925k.

DOI:10.1039/d2an00925k
PMID:36040388
Abstract

The present work describes the application of an in-house developed 3D-printed open port probe (3DP-OPP) with differential ion mobility spectrometry (DMS) mass spectrometry. Targeted quantitative analysis in urine was performed with a triple quadrupole mass spectrometer in the selected reaction monitoring mode (OPP-DMS-SRM/MS) and illicit pill screening using data independent acquisition (OPP-DMS-SWATH/MS). The combination of compensation voltage (CoV) scanning in DMS using modifiers with SWATH/MS acquisition for MS/MS spectrum generation enabled the differentiation of isobaric signals with a large dynamic range and enhance the information contained in the screening of illicit ecstasy pills. As for any direct MS introduction technique where no chromatographic separation is applied DMS with acetonitrile as a modifier allows the separation of cocaine and tramadol, and their isomeric metabolites in urine samples. Quantitative application using OPP-DMS-SRM/MS is presented without the need for sample preparation with a lower limit of quantification at 10-25 ng mL for the analytes and less than 40 seconds for sample to sample analysis.

摘要

本研究描述了一种内部开发的3D打印开口端口探针(3DP-OPP)与差分离子迁移谱(DMS)质谱联用的应用。在选定反应监测模式下,使用三重四极杆质谱仪对尿液进行靶向定量分析(OPP-DMS-SRM/MS),并使用数据非依赖采集进行非法药丸筛查(OPP-DMS-SWATH/MS)。在DMS中使用修饰剂进行补偿电压(CoV)扫描与用于生成MS/MS谱的SWATH/MS采集相结合,能够在大动态范围内区分等压信号,并增强非法摇头丸筛查中包含的信息。对于任何不应用色谱分离的直接质谱进样技术,以乙腈作为修饰剂的DMS可实现尿液样品中可卡因和曲马多及其异构体代谢物的分离。本文介绍了使用OPP-DMS-SRM/MS的定量应用,无需样品前处理,分析物的定量下限为10 - 25 ng/mL,样品间分析时间少于40秒。

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