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  4. Quantification of clenbuterol at trace level in human urine by ultra-high pressure liquid chromatography-tandem mass spectrometry.
 
  • Détails
Titre

Quantification of clenbuterol at trace level in human urine by ultra-high pressure liquid chromatography-tandem mass spectrometry.

Type
article
Institution
UNIL/CHUV/Unisanté + institutions partenaires
Périodique
Journal of Chromatography A  
Auteur(s)
Nicoli, R.
Auteure/Auteur
Petrou, M.
Auteure/Auteur
Badoud, F.
Auteure/Auteur
Dvorak, J.
Auteure/Auteur
Saugy, M.
Auteure/Auteur
Baume, N.
Auteure/Auteur
Liens vers les personnes
Baume, Norbert  
Saugy, Martial  
Nicoli, Raul  
Liens vers les unités
Médecine légale (CURML)  
Laboratoire d'analyse du dopage (LAD)  
ISSN
1873-3778
Statut éditorial
Publié
Date de publication
2013
Volume
1292
Première page
142
Dernière page/numéro d’article
150
Langue
anglais
Notes
Publication types: Journal Article ; Validation Studies
Publication Status: ppublish
Résumé
Clenbuterol is a β2 agonist agent with anabolic properties given by the increase in the muscular mass in parallel to the decrease of the body fat. For this reason, the use of clenbuterol is forbidden by the World Anti-Doping Agency (WADA) in the practice of sport. This compound is of particular interest for anti-doping authorities and WADA-accredited laboratories due to the recent reporting of risk of unintentional doping following the eating of meat contaminated with traces of clenbuterol in some countries. In this work, the development and the validation of an ultra-high pressure liquid chromatography coupled to electrospray ionization tandem mass spectrometry (UHPLC-ESI-MS/MS) method for the quantification of clenbuterol in human urine is described. The analyte was extracted from urine samples by liquid-liquid extraction (LLE) in basic conditions using tert butyl-methyl ether (TBME) and analyzed by UHPLC-MS/MS with a linear gradient of acetonitrile in 9min only. The simple and rapid method presented here was validated in compliance with authority guidelines and showed a limit of quantification at 5pg/mL and a linearity range from 5pg/mL to 300pg/mL. Good trueness (85.8-105%), repeatability (5.7-10.6% RSD) and intermediate precision (5.9-14.9% RSD) results were obtained. The method was then applied to real samples from eighteen volunteers collecting urines after single oral doses administration (1, 5 and 10μg) of clenbuterol-enriched yogurts.
Sujets

Adrenergic beta-Agoni...

Chromatography, High ...

Clenbuterol/urine

Doping in Sports

Food Contamination/an...

Humans

Liquid-Liquid Extract...

Male

Sensitivity and Speci...

Spectrometry, Mass, E...

Tandem Mass Spectrome...

PID Serval
serval:BIB_04EB599A9A44
DOI
10.1016/j.chroma.2012.12.008
PMID
23294994
WOS
000319237100014
Permalien
https://iris.unil.ch/handle/iris/61725
Date de création
2013-02-12T14:55:37.604Z
Date de création dans IRIS
2025-05-20T15:35:51Z
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