4.2 Article

A simplified procedure for GC/C/IRMS analysis of underivatized 19-norandrosterone in urine following HPLC purification

Journal

STEROIDS
Volume 76, Issue 5, Pages 471-477

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.steroids.2011.01.001

Keywords

19-Norandrosterone; Isotope ratio mass spectrometry (IRMS); HPLC sample preparation

Funding

  1. Italian Department of Health (Ministero della Salute, Commissione per la vigilanza sul doping e sulla tutela sanitaria delle attivita sportive)

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Nandrolone and/or its precursors are included in the World Anti-doping Agency (WADA) list of forbidden substances and methods and as such their use is banned in sport. 19-Norandrosterone (19-NA) the main metabolite of these compounds can also be produced endogenously. The need to establish the origin of 19-NA in human urine samples obliges the antidoping laboratories to use isotope ratio mass spectrometry (IRMS) coupled to gas chromatography (GC/C/IRMS). In this work a simple liquid chromatographic method without any additional derivatization step is proposed, allowing to drastically simplify the urine pretreatment procedure. leading to extracts free of interferences permitting precise and accurate IRMS analysis. The purity of the extracts was verified by parallel analysis by gas chromatography coupled to mass spectrometry with GC conditions identical to those of the GC/C/IRMS assay. The method has been validated according to 15017025 requirements (within assay precision of +/- 0.3 parts per thousand and between assay precision of +/- 0.4 parts per thousand). The method has been tested with samples obtained after the administration of synthetic 19-norandrostenediol and samples collected during pregnancy where 19-NA is known to be produced endogenously. Twelve drugs and synthetic standards able to produce through metabolism 19-NA have shown to present delta C-13 values around -29 parts per thousand being quite homogeneous (-28.8 +/- 1.5; mean +/- standard deviation) while endogenously produced 19-NA has shown values comparable to other endogenous produced steroids in the range -21 to -24 parts per thousand as already reported. The efficacy of the method was tested on real samples from routine antidoping analyses. (C) 2011 Elsevier Inc. All rights reserved.

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