Premium
Detecting the abuse of 19‐norsteroids in doping controls: A new gas chromatography coupled to isotope ratio mass spectrometry method for the analysis of 19‐norandrosterone and 19‐noretiocholanolone
Author(s) -
Iannella Loredana,
Colamonici Cristiana,
Curcio Davide,
Botrè Francesco,
Torre Xavier
Publication year - 2021
Publication title -
drug testing and analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.065
H-Index - 54
eISSN - 1942-7611
pISSN - 1942-7603
DOI - 10.1002/dta.2985
Subject(s) - chromatography , chemistry , isotope ratio mass spectrometry , mass spectrometry , nandrolone , gas chromatography , urine , pregnanediol , detection limit , gas chromatography–mass spectrometry , isotope dilution , biochemistry , anabolism
The detection of 19‐norsteroids abuse in doping controls currently relies on the determination of 19‐norandrosterone (19‐NA) by gas chromatography–tandem mass spectrometry (GC–MS/MS). An additional confirmatory analysis by gas chromatography coupled to isotope ratio mass spectrometry (GC‐C‐IRMS) is performed on samples showing 19‐NA concentrations between 2.5 and 15 ng/ml and not originated from pregnant female athletes or female treated with 19‐norethisterone. 19‐Noretiocholanolone (19‐NE) is typically produced to a lesser extent as a secondary metabolite. The aim of this work was to improve the GC‐C‐IRMS confirmation procedure for the detection of 19‐norsteroids misuse. Both 19‐NA and 19‐NE were analyzed as target compounds (TCs), whereas androsterone (A), pregnanediol (PD), and pregnanetriol (PT) were selected as endogenous reference compounds (ERCs). The method was validated and applied to urine samples collected by three male volunteers after the administration of nandrolone‐based formulations. Before the instrumental analysis, urine samples (<25 ml) were hydrolyzed with β‐glucuronidase from Escherichia coli and extracted with n ‐pentane. Compounds of interest were purified through a single (for PT) or double (for 19‐NE, 19‐NA, A, and PD) liquid chromatographic step, to reduce the background noise and eliminate interferences that could have affect the accuracy of δ 13 C values. The limit of quantification (LOQ) of 2 ng/ml was ensured for both 19‐NA and 19‐NE. The 19‐NE determination could be helpful in case of “unstable” urine samples, in late excretion phases or when coadministration with 5α‐reductase inhibitors occur.