The detection of the abuse of pseudoendogenous steroids (testosterone and/or its precursors) is currently based, when possible, on the application of the steroid module of the World Anti-Doping Agency (WADA), athlete biological passport (ABP), implemented through the global database, ADAMS. When a suspicious sample is detected, the confirmation by isotope ratio mass spectrometry (IRMS) is required. It is well known that this confirmation procedure is time consuming and expensive and can be only applied on a reduced number of samples. In previous studies we have demonstrated that the longitudinal evaluation of the IRMS data is able to detect positive samples that otherwise will be evaluated as negative, improving the efficacy of the fight against doping in sport. This would require the analysis of a much larger volume of samples by IRMS. The aim of the present work is to describe an IRMS screening method allowing to increase the throughput of samples that can be analyzed by IRMS. The detection efficacy of the method is compared with the confirmation method in use, and to assess its robustness and applicability, all the samples of a major cycling stage competition were analyzed, with the agreement of the testing authority, under routine conditions and response times. The results obtained permit to conclude that the IRMS screening method here proposed has adequate selectivity and produces results that overlap with the already validated method currently in use permitting to analyze a much higher volume of samples even during a major event without compromising the detection capacity. Copyright © 2017 John Wiley & Sons, Ltd.

Fast IRMS screening of pseudoendogenous steroids in doping analyses / de la Torre, Xavier; Colamonici, Cristiana; Curcio, Davide; Botrè, Francesco. - In: DRUG TESTING AND ANALYSIS. - ISSN 1942-7603. - STAMPA. - 9:11-12(2017), pp. 1804-1812. [10.1002/dta.2321]

Fast IRMS screening of pseudoendogenous steroids in doping analyses

Curcio, Davide;Botrè, Francesco
2017

Abstract

The detection of the abuse of pseudoendogenous steroids (testosterone and/or its precursors) is currently based, when possible, on the application of the steroid module of the World Anti-Doping Agency (WADA), athlete biological passport (ABP), implemented through the global database, ADAMS. When a suspicious sample is detected, the confirmation by isotope ratio mass spectrometry (IRMS) is required. It is well known that this confirmation procedure is time consuming and expensive and can be only applied on a reduced number of samples. In previous studies we have demonstrated that the longitudinal evaluation of the IRMS data is able to detect positive samples that otherwise will be evaluated as negative, improving the efficacy of the fight against doping in sport. This would require the analysis of a much larger volume of samples by IRMS. The aim of the present work is to describe an IRMS screening method allowing to increase the throughput of samples that can be analyzed by IRMS. The detection efficacy of the method is compared with the confirmation method in use, and to assess its robustness and applicability, all the samples of a major cycling stage competition were analyzed, with the agreement of the testing authority, under routine conditions and response times. The results obtained permit to conclude that the IRMS screening method here proposed has adequate selectivity and produces results that overlap with the already validated method currently in use permitting to analyze a much higher volume of samples even during a major event without compromising the detection capacity. Copyright © 2017 John Wiley & Sons, Ltd.
2017
doping in sports; high throughput; isotope ratio mass spectrometry (IRMS); Analytical Chemistry; Environmental Chemistry; 3003; Spectroscopy
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Fast IRMS screening of pseudoendogenous steroids in doping analyses / de la Torre, Xavier; Colamonici, Cristiana; Curcio, Davide; Botrè, Francesco. - In: DRUG TESTING AND ANALYSIS. - ISSN 1942-7603. - STAMPA. - 9:11-12(2017), pp. 1804-1812. [10.1002/dta.2321]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1121545
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