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Electron ionization mass spectrometry of the ryanodine receptor‐based Ca 2+ ‐channel stabilizer S‐107 and its implementation into routine doping control
Author(s) -
Thevis Mario,
Beuck Simon,
Thomas Andreas,
Fußhöller Gregor,
Sigmund Gerg,
Schlörer Nils,
Rodchenkov Grigory,
Schäfer Mathias,
Schänzer Wilhelm
Publication year - 2009
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.4161
Subject(s) - chemistry , ryanodine receptor , mass spectrometry , analyte , chromatography , electron ionization , tandem mass spectrometry , liquid chromatography–mass spectrometry , ionization , intracellular , biochemistry , organic chemistry , ion
New insights into the biochemistry of cardiac arrhythmia and skeletal muscle fatigue have yielded new drug candidates to counteract these phenomena. Major biological targets have become ryanodine receptor (RyR)‐based Ca 2+ ‐release channels, which tend to ‘leak’ under various circumstances including strenuous exercise and, thus, cause aberrant calcium sparks that entail impaired muscle function. Therapeutics, which are referred to as rycals, are currently being developed to treat cardiac arrhythmia via enhancement of calstabin‐ryanodine affinities that causes a stabilization of the RyR. These therapeutics possess potential for misuse in sports, and an early implementation of target analytes such as the benzothiazepine derivatives S‐107 and JTV‐519 or putative metabolites into doping control screening procedures is recommended. Reference compounds, deuterated analogues, and a putative metabolic product were synthesized, and electron ionization mass spectra of these products were studied and dissociation pathways elucidated by means of tandem mass spectrometry (MS/MS) and accurate mass measurements. The characterized analytes were incorporated into existing sports drug testing assays based on liquid‐liquid extraction and subsequent gas chromatography/mass spectrometry (GC/MS) analysis, and specificity, lower limit of detection (4–6 ng/mL), intraday and interday precision (1.5–17.2%), as well as recovery (63–66%) were determined. The established procedure proved suitable for routine doping control analysis to detect a potential misuse of the drug candidate S‐107 in elite sport. Copyright © 2009 John Wiley & Sons, Ltd.