Effect of microbial degradation on steroid profile and IRMS analysis : a case study

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Deutscher übersetzter Titel:Die Auswirkungen von mikrobieller Degradierung auf Steroidprofil und IRMS-Analyse : eine Fallstudie
Autor:Jain, S.; Nimker, V.; Shrivastava, A.; Jamal, H.; Lal, R.; Kaur, T.; Beotra, A.; Shukla, S.
Erschienen in:Recent advances in doping analysis (22) : Proceedings of the Manfred-Donike-Workshop ; 32nd Cologne Workshop on Dope Analysis ; 30th March to 4th April 2014
Veröffentlicht:Köln: Sportverl. Strauß (Verlag), 2014, S. 141-145, Lit.
Format: Literatur (SPOLIT)
Publikationstyp: Sammelwerksbeitrag
Medienart: Elektronische Ressource (Datenträger)
Dokumententyp: Tagungsband
Sprache:Englisch
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Erfassungsnummer:PU201702001180
Quelle:BISp

Abstract des Autors

Effect of microbial degradation on the steroid profile in urine samples has been well investigated but not much is known about its effects on carbon isotope ratios. Transportation of urine samples, collected for doping control analysis does not always meet ideal conditions of storage which may stimulate bacterial contamination affecting urinary steroids concentration. According to WADA technical document TD2004 EAAS (valid till Dec. 2013), the presence of bacterial degradation and free steroids invalidate the urine sample for reporting Adverse Analytical Findings (AAF). This paper presents result of one sample received from an international client in 2013, which showed signs of bacterial degradation (presence of high concentration of 4-androstendione, and 5α and 5β-androstanedione and a T/E ratio >10). Further investigation showed that most of the endogenous steroids excreted were in free form (more than 50%) implying a strong indication of degradation. The influence of bacterial degradation on CIR of different urinary steroids was investigated in the combined, unconjugated and conjugated fractions. The peak heights and δ13C values of urinary steroids in the combined fraction were comparable with those observed in the free fraction. The GC/C/IRMS analysis was consistent with exogenous origin of endogenous steroids, meeting the criteria to report an AAF. This sample could not be reported as AAF as all the target compounds were present in un-conjugated form, thereby not meeting WADA criteria of reporting AAF. Further work is in progress with more number of samples to ascertain that CIR is independent of influence of bacterial growth affecting steroid profile.