2021
DOI: 10.1016/j.chroma.2021.462039
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Enabling the inclusion of non-hydrolysed sulfated long term anabolic steroid metabolites in a screening for doping substances by means of gas chromatography quadrupole time-of-flight mass spectrometry

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Cited by 11 publications
(9 citation statements)
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“…The combined sample procedure has been previously published 22 . Briefly, 0.5 ml of urine was aliquoted to two separate tubes, labelled A and B for the combined non‐hydrolysed sulphate fraction and hydrolysed glucuronated fraction.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The combined sample procedure has been previously published 22 . Briefly, 0.5 ml of urine was aliquoted to two separate tubes, labelled A and B for the combined non‐hydrolysed sulphate fraction and hydrolysed glucuronated fraction.…”
Section: Methodsmentioning
confidence: 99%
“…As such, the core structure of the steroid molecule remains intact, facilitating detection, characterisation and confirmation of the steroid by for example further fragmentation to obtain more compound‐specific ions. Recently, a new straightforward sample preparation procedure was published, consisting of the combination of two liquid–liquid extractions (LLE), that enabled the simultaneous detection of non‐hydrolysed sulphated steroids and the conventional steroid metabolites in the same GC–MS run 22 …”
Section: Introductionmentioning
confidence: 99%
“…In the measurement of anabolic androgenic steroids (AASs) analyzed with high frequency in previous years, the conjugated steroids are often used as target analytes for the steroids conventionally. In a previous report, sulfated metabolites were found to have a long detectable time [84]. Simultaneous analysis of the sulphated AASs and the other mandatory targets was proposed using full scan high resolution GClow energy electron ionization (LEEI)-MS, with the sample procedure consisting of two liquid-liquid extraction (LLE).…”
Section: Ms 41 Gc-msmentioning
confidence: 99%
“…Testing comprehensively and sensitively for hundreds of target analytes remains mandatory in sports drug testing, and ITP performance characteristics are continuously optimized, as, for example, shown by Albertsdottir et al 42 Here, two urine sample extracts, one obtained by liquid‐liquid extraction (LLE), and one produced by enzymatic hydrolysis employing β‐glucuronidase and subsequent LLE were combined prior to trimethylsilylation and GC/EI/QTOF analysis. The instrument was equipped with a 15 m × 200 μm (inner diameter) capillary column with a film thickness of 0.11 μm, and EI was conducted using 18 eV followed by full scan mass spectrometry ( m/z 50–750).…”
Section: Anabolic Agentsmentioning
confidence: 99%