4.4 Article

Evaluation of alternative gas chromatographic and mass spectrometric behaviour of trimethylsilyl-derivatives of non-hydrolysed sulfated anabolic steroids

Journal

DRUG TESTING AND ANALYSIS
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1002/dta.3462

Keywords

doping; gas chromatography; mass spectrometry; steroids; sulfates

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Sulfated metabolites have the potential to serve as long-term markers of anabolic-androgenic steroid abuse. Gas chromatography-mass spectrometry (GC-MS) is compatible with trimethylsilyl (TMS)-derivatives of non-hydrolysed sulfated steroids. However, sulfated reference standards are limited, and the GC-MS behavior of these compounds is mainly based on analyzing available standard reference material. In order to investigate this, in-house sulfated reference materials resembling known sulfated long-term markers were analyzed on GC-MS, and the gas chromatographic and mass spectrometric behavior was mapped and linked to the corresponding steroid structures.
Sulfated metabolites have shown to have potential as long-term markers (LTMs) of anabolic-androgenic steroid (AAS) abuse. The compatibility of gas chromatography-mass spectrometry (GC-MS) with trimethylsilyl (TMS)-derivatives of non-hydrolysed sulfated steroids has been demonstrated, where, after derivatisation, generally, two closely eluting isomers are formed that both have the same molecular ion [M-H2SO4](center dot+). Sulfated reference standards are in limited commercial availability, and therefore, the current knowledge of the GC-MS behaviour of these compounds is mainly based on sulfating and analysing the available standard reference material. This procedure can unfortunately not cover all of the current known LTMs as these are often not available as pure substance. Therefore, in theory, some metabolites could be missed as they exhibit alternative behaviour. To investigate the matter, in-house sulfated reference materials that bear resemblance to known sulfated LTMs were analysed on GC-MS in their TMS-derivatised non-hydrolysed state. The (alternative) gas chromatographic and mass spectrometric behaviour was mapped, evaluated and linked to the corresponding steroid structures. Afterwards, using fraction collection, known sulfated LTMs were isolated from excretion urine to confirm the observed findings. The categories that were selected were mono-hydroxy-diones, 17-methyl-3,17-diols and 17-keto-3,16-diols as these are commonly encountered AAS conformations. The ability to predict the GC-MS behaviour of non-hydrolysed sulfated AAS metabolites is the corner stone of finding new metabolites. This knowledge is also essential, for example, for understanding AAS detection analyses, for the mass spectrometric characterization of metabolites of new designer steroids or when one needs to characterize an unknown steroid structure.

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