Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.
Post Graduate and Research Department of Chemistry, Jamal Mohamed College (Affiliated to Bharathidasan University), Tiruchirappalli, Tamil Nadu, India.
Drug Test Anal. 2023 Jul;15(7):757-768. doi: 10.1002/dta.3469. Epub 2023 Mar 27.
Nonsteroidal selective androgen receptor modulators (SARMs) are a novel class of compounds that have not yet been clinically approved; however, they appear to have a better anabolic/androgenic ratio than steroids and cause slighter side effects. Sports drug testing laboratories are required to maintain continuously updated doping control analytical methods in light of the widespread misuse of SARMs in elite and amateur sports. This paper describes the metabolic conversion of SARM GSK2881078 in thoroughbred horses following oral administration and in vitro with equine liver microsomes. A liquid chromatography-high-resolution mass spectrometry method was used to postulate the plausible structures of the detected metabolites. A total of five (M1-M5) in vivo metabolites and six (M1-M6) in vitro metabolites were detected under experimental conditions. Phase I metabolites mainly result from hydroxylation. Methoxylated and side-chain dissociated metabolites were also detected. Neither sulfonic acid nor glucuronic acid conjugated metabolites were observed in this study. Data reported here could aid in the detection of nonsteroidal SARM GSK2881078 and reveal its illicit use in competitive sports.
非甾体选择性雄激素受体调节剂 (SARMs) 是一类尚未获得临床批准的新型化合物;然而,它们似乎具有比类固醇更好的合成代谢/雄激素比值,并且副作用较小。鉴于 SARMs 在精英和业余运动中的广泛滥用,体育药物检测实验室需要不断更新兴奋剂控制分析方法。本文描述了口服和马肝微粒体体外给予 SARM GSK2881078 后,在纯种马体内的代谢转化。采用液相色谱-高分辨质谱法推测了检测到的代谢物的可能结构。在实验条件下共检测到五种(M1-M5)体内代谢物和六种(M1-M6)体外代谢物。I 相代谢物主要来源于羟化。还检测到甲氧基化和侧链解离的代谢物。在本研究中未观察到磺酸或葡萄糖醛酸结合的代谢物。本文报道的数据有助于非甾体 SARM GSK2881078 的检测,并揭示其在竞技体育中的非法使用。