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超高效液相色谱-四极杆飞行时间质谱法快速分析尿液中的兴奋剂。二:确证分析。

Fast analysis of doping agents in urine by ultra-high-pressure liquid chromatography-quadrupole time-of-flight mass spectrometry. II: Confirmatory analysis.

机构信息

Swiss Laboratory for Doping Analyses, University Center of Legal Medicine, Geneva and Lausanne, Chemin des Croisettes 22, 1066 Epalinges, Switzerland.

出版信息

J Chromatogr A. 2010 Jun 18;1217(25):4109-19. doi: 10.1016/j.chroma.2009.11.001. Epub 2009 Nov 10.

Abstract

For doping control, analyses of samples are generally achieved in two steps: a rapid screening and, in the case of a positive result, a confirmatory analysis. A two-step methodology based on ultra-high-pressure liquid chromatography coupled to a quadrupole time-of-flight mass spectrometry (UHPLC-QTOF-MS) was developed to screen and confirm 103 doping agents from various classes (e.g., beta-blockers, stimulants, diuretics, and narcotics). The screening method was presented in a previous article as part I (i.e., Fast analysis of doping agents in urine by ultra-high-pressure liquid chromatography-quadrupole time-of-flight mass spectrometry. Part I: screening analysis). For the confirmatory method, basic, neutral and acidic compounds were extracted by a dedicated solid-phase extraction (SPE) in a 96-well plate format and detected by MS in the tandem mode to obtain precursor and characteristic product ions. The mass accuracy and the elemental composition of precursor and product ions were used for compound identification. After validation including matrix effect determination, the method was considered reliable to confirm suspect results without ambiguity according to the positivity criteria established by the World Anti-Doping Agency (WADA). Moreover, an isocratic method was developed to separate ephedrine from its isomer pseudoephedrine and cathine from phenylpropanolamine in a single run, what allowed their direct quantification in urine.

摘要

用于兴奋剂检测,样品分析通常分为两步进行:快速筛选,以及在阳性结果的情况下进行确证分析。本文建立了一种两步法,基于超高效液相色谱-四极杆飞行时间质谱联用(UHPLC-QTOF-MS),用于筛选和确证来自不同类别(如β受体阻滞剂、兴奋剂、利尿剂和麻醉剂)的 103 种兴奋剂。该筛选方法已于前一篇文章中报道,作为第一部分(即:超高效液相色谱-四极杆飞行时间质谱法快速分析尿液中的兴奋剂。第一部分:筛选分析)。对于确证方法,碱性、中性和酸性化合物通过专用的 96 孔板固相萃取(SPE)进行提取,并在串联模式下通过 MS 进行检测,以获得前体离子和特征产物离子。前体离子和产物离子的质量精度和元素组成用于化合物鉴定。该方法经过验证,包括基质效应的确定,被认为可靠,可以根据世界反兴奋剂机构(WADA)建立的阳性标准,对可疑结果进行确证,而不会产生歧义。此外,还开发了一种等度方法,可在单次运行中分离麻黄碱与其异构体伪麻黄碱,以及去甲麻黄碱与苯丙醇胺,从而可直接对尿液中的这些物质进行定量。

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