کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1163029 1490917 2016 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Fast and sensitive supercritical fluid chromatography – tandem mass spectrometry multi-class screening method for the determination of doping agents in urine
ترجمه فارسی عنوان
کروماتوگرافی سیال سریع و حساس فوق بحرانی روش غربالگری چند منظوره اسپکترومتری دو طرفه برای تعیین عوامل دوپینگ در ادرار
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• A high throughput UHPSFC-MS/MS method was developed for screening several classes of doping agents in urine.
• Supported liquid extraction in 48-well plate format was successfully applied to extract the doping agents from urine samples.
• Good extraction recoveries and reasonable matrix effects were observed for the whole set of doping agents.
• The method exhibited very low LODs, below the Minimum Required Performance Levels, for most of the 100 compounds.

This study shows the possibility offered by modern ultra-high performance supercritical fluid chromatography combined with tandem mass spectrometry in doping control analysis. A high throughput screening method was developed for 100 substances belonging to the challenging classes of anabolic agents, hormones and metabolic modulators, synthetic cannabinoids and glucocorticoids, which should be detected at low concentrations in urine. To selectively extract these doping agents from urine, a supported liquid extraction procedure was implemented in a 48-well plate format. At the tested concentration levels ranging from 0.5 to 5 ng/mL, the recoveries were better than 70% for 48–68% of the compounds and higher than 50% for 83–87% of the tested substances. Due to the numerous interferences related to isomers of steroids and ions produced by the loss of water in the electrospray source, the choice of SFC separation conditions was very challenging. After careful optimization, a Diol stationary phase was employed. The total analysis time for the screening assay was only 8 min, and interferences as well as susceptibility to matrix effect (ME) were minimized. With the developed method, about 70% of the compounds had relative ME within the range ±20%, at a concentration of 1 and 5 ng/mL. Finally, limits of detection achieved with the above-described strategy including 5-fold preconcentration were below 0.1 ng/mL for the majority of the tested compounds. Therefore, LODs were systematically better than the minimum required performance levels established by the World anti-doping agency, except for very few metabolites.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Analytica Chimica Acta - Volume 915, 7 April 2016, Pages 102–110
نویسندگان
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