Metabolism of boldione in humans by mass spectrometric techniques: detection of pseudoendogenous metabolites.

Boldione is an anabolic androgenic steroid (AAS) related to boldenone, androstenedione, and testosterone bearing two double bonds in C1 and C4 positions. Boldione is rapidly transformed to the well-known AAS boldenone, being both compounds included in the list of prohibited substances and methods published yearly by the World Anti-Doping Agency (WADA). After the administration of boldione to a male volunteer, the already described urinary metabolites of boldenone produced after reduction in C4, oxydoreduction in C3 and C17, and hydroxylation have been detected. In addition, minor new metabolites have been detected and their structure postulated after mass spectrometric analyses. Finally, the reduction of the double bound in C1 produces metabolites identical to the endogenously produced ones. A method based on gas chromatography coupled to isotope ratio mass spectrometry (GC/C/IRMS) after a urine sample purification by high performance liquid chromatography (HPLC) permitted to confirm the main synthetic like boldione/boldenone metabolite (17β-hydroxy-5β-androst-1-en-3-one) and boldenone at trace levels (< 5 ng/mL) and then to establish its synthetic or endogenous origin, and to determine the exogenous origin of metabolites with the same chemical structure of the endogenous ones. The detection of pseudoendogenous androgens of synthetic origin partially overlapped boldenone and its main metabolite detection, being an additional proof of synthetic steroids misuse. By the use of IRMS, the correct evaluation of the modifications of the steroid profile after the administration of synthetic AAS that could be converted into endogenous like ones is possible.

[1]  Shahram Mohaghegh,et al.  Doping and the Latest Prohibited List of the World Anti-Doping Agency (WADA) , 2013 .

[2]  X. de la Torre,et al.  A comprehensive procedure based on gas chromatography-isotope ratio mass spectrometry following high performance liquid chromatography purification for the analysis of underivatized testosterone and its analogues in human urine. , 2012, Analytica chimica acta.

[3]  Ó. Pozo,et al.  Detection and characterization of urinary metabolites of boldione by LC-MS/MS. Part I: Phase I metabolites excreted free, as glucuronide and sulfate conjugates, and released after alkaline treatment of the urine. , 2012, Drug testing and analysis.

[4]  Ó. Pozo,et al.  Detection and characterization of urinary metabolites of boldione by LC-MS/MS. Part II: Conjugates with cysteine and N-acetylcysteine. , 2012, Drug testing and analysis.

[5]  H. Geyer,et al.  Seized designer supplement named “1-Androsterone”: Identification as 3β-hydroxy-5α-androst-1-en-17-one and its urinary elimination , 2011, Steroids.

[6]  F. Botrè,et al.  A simplified procedure for GC/C/IRMS analysis of underivatized 19-norandrosterone in urine following HPLC purification , 2011, Steroids.

[7]  X. de la Torre,et al.  Urine stability and steroid profile: towards a screening index of urine sample degradation for anti-doping purpose. , 2011, Analytica chimica acta.

[8]  H. Geyer,et al.  Determination of (13)C/(12)C ratios of urinary excreted boldenone and its main metabolite 5beta-androst-1-en-17beta-ol-3-one. , 2010, Drug testing and analysis.

[9]  L. Vanhaecke,et al.  Endogenous boldenone-formation in cattle: Alternative invertebrate organisms to elucidate the enzymatic pathway and the potential role of edible fungi on cattle's feed , 2010, The Journal of Steroid Biochemistry and Molecular Biology.

[10]  W. Schänzer,et al.  Metabolism of androsta-1,4,6-triene-3,17-dione and detection by gas chromatography/mass spectrometry in doping control. , 2009, Rapid communications in mass spectrometry : RCM.

[11]  E. Ferrer,et al.  Evaluation of boldenone formation and related steroids transformations in veal faeces by liquid chromatography/tandem mass spectrometry. , 2008, Rapid communications in mass spectrometry : RCM.

[12]  C. V. Van Peteghem,et al.  Determination of anabolic steroids in dietary supplements by liquid chromatography-tandem mass spectrometry. , 2007, Analytica chimica acta.

[13]  G. Biancotto,et al.  An in vitro study on metabolism of 17beta-boldenone and boldione using cattle liver and kidney subcellular fractions. , 2007, Analytica chimica acta.

[14]  F. Monteau,et al.  Criteria to distinguish between natural situations and illegal use of boldenone, boldenone esters and boldione in cattle 1. Metabolite profiles of boldenone, boldenone esters and boldione in cattle urine , 2006, Steroids.

[15]  Yunje Kim,et al.  Characterization of boldione and its metabolites in human urine by liquid chromatography/electrospray ionization mass spectrometry and gas chromatography/mass spectrometry. , 2006, Rapid communications in mass spectrometry : RCM.

[16]  A. Terracciano,et al.  Detection of boldenone and its major metabolites by liquid chromatography—tandem mass spectrometry in urine samples , 2005 .

[17]  C. Reilly,et al.  Analysis of the nutritional supplement 1AD, its metabolites, and related endogenous hormones in biological matrices using liquid chromatography-tandem mass spectrometry. , 2004, Journal of analytical toxicology.

[18]  R. de la Torre,et al.  Changes in androgenic steroid profile due to urine contamination by microorganisms: a prospective study in the context of doping control. , 2001, Analytical biochemistry.

[19]  M. Donike,et al.  Metabolism of anabolic steroids in man: synthesis and use of reference substances for identification of anabolic steroid metabolites , 1993 .

[20]  M. Donike,et al.  Metabolism of boldenone in man: gas chromatographic/mass spectrometric identification of urinary excreted metabolites and determination of excretion rates. , 1992, Biological mass spectrometry.