4.7 Article

A uniform sample preparation procedure for gas chromatography combustion isotope ratio mass spectrometry for all human doping control relevant anabolic steroids using online 2/3-dimensional liquid chromatography fraction collection

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ANALYTICA CHIMICA ACTA
卷 1168, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.aca.2021.338610

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Doping control; Isotope ratio mass spectrometry; Multi-dimensional liquid chromatography; Steroids; Testosterone; Boldenone

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Androgenic anabolic steroids are misused in sports for their performance-enhancing effects. Gas Chromatography Combustion Isotope Ratio Mass Spectrometry (GC-C-IRMS) is used to determine their origin. The clean-up of compounds for analysis is challenging due to low concentrations and matrix effects.
Androgenic anabolic steroids are the most misused substances in sports because of their performanceenhancing effects. Often synthetic analogues of endogenously present steroids are administered. To determine their endogenous or exogenous origin, Gas Chromatography Combustion Isotope Ratio Mass Spectrometry (GC-C-IRMS) is used in the field of doping control. Compounds subjected to IRMS analysis must be interference-free, with liquid chromatography fraction collection (HPLC-FC) being the crucial clean-up step. However, this clean-up is challenging, particularly for compounds present at low concentrations in samples with pronounced matrix effects. The compounds of interests for IRMS analyses in doping control are testosterone (T) and its main metabolites (androsterone, etiocholanolone, 5aandrostane-3a,170-diol, 50-androstane-3a,170-diol), epitestosterone, 19-norandrosterone (19-NA), boldenone (B) and its main metabolite (BM), formestane (F) and 6aOH-androstenedione (6aOHADION). Currently, the available methods only deal with a selection of the above-mentioned compounds. Some of these compounds (e.g., 19-NA, B, BM, 6aOHADION) are present in very low concentrations, requiring an extensive and dedicated sample clean-up, and this makes it challenging to develop a universal clean-up procedure. Many of these methods require different and multiple offline HPLC-FC setups, which are labour-intensive and time-consuming. That is problematic during, e.g., large sports events, where reporting time is limited (e.g., 72 h). Therefore, in the current work, we developed a uniform online 2D/ 3D HPLC-FC method, capable of purifying all relevant target compounds in a single run, leading to the fastest clean-up procedure so far (i.e., 31 min for T and its main metabolites; 46 min for 19-NA, F and 6aOHADION; 48 min for B and BM). (c) 2021 Elsevier B.V. All rights reserved.

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