Institute of Biochemistry-Center for Preventive Doping Research, German Sport University Cologne, Cologne, Germany.
Rapid Commun Mass Spectrom. 2013 May 15;27(9):993-1004. doi: 10.1002/rcm.6539.
The recent discovery of resveratrol's capability to inhibit cAMP-specific phosphodiesterases (PDEs) and, as a consequence, to enhance particularly the activity of Sirt1 in animal models has reinforced the interest of preventive doping research organizations, especially in PDE4 inhibitors. Among these, the archetypical PDE4-inhibitor rolipram significantly increased the number of mitochondria in laboratory rodents, which further demonstrated a performance increase in a treadmill-test (time-to-exhaustion) of approximately 40%. Besides rolipram, a variety of new PDE4-inhibiting substances including cilomilast, roflumilast, and numerous additional new drug entities were described, with roflumilast being the first-in-class having received clinical approval for the treatment of chronic obstructive pulmonary disease (COPD). Due to the availability of these substances, and the fact that a misuse of such compounds in sport cannot be excluded, it deems relevant to probe for the prevalence of these compounds in sports drug testing programs.
Known urinary phase-I metabolites of rolipram, roflumilast, and cilomilast were generated by in vitro incubations employing human liver microsomal preparations. The metabolites obtained were studied by liquid chromatography with high-resolution/high-accuracy tandem mass spectrometry (LC/MS/MS) and the reference product ion mass spectra of established and most relevant metabolites were utilized to provide the information necessary for comprehensive doping controls. The analytical procedure was based on conventional routine doping control assays employing enzymatic hydrolysis followed by liquid-liquid extraction and subsequent LC/MS/MS measurement.
Structures of diagnostic product ions and dissociation pathways of target analytes were elucidated, providing the information required for implementation into an existing test method for routine sports drug testing. The established method allowed for detection limits for the intact drugs of 1-5 ng/mL, and further assay characteristics (intraday precision 1.5-13.7%, interday precision 7.3-18.6%, recovery 20-100%, ion suppression/enhancement, and specificity) were determined. In addition, proof-of-concept analyses concerning roflumilast were conducted with a urine sample obtained from a COPD patient under roflumilast treatment.
最近发现白藜芦醇能够抑制 cAMP 特异性磷酸二酯酶(PDEs),并因此特别增强 Sirt1 的活性,这一发现增强了预防兴奋剂研究组织的兴趣,尤其是对 PDE4 抑制剂。在这些抑制剂中,典型的 PDE4 抑制剂罗利普兰显著增加了实验室啮齿动物的线粒体数量,这进一步证明了在跑步机测试(疲劳时间)中大约提高了 40%的运动表现。除了罗利普兰,还描述了许多新的 PDE4 抑制物质,包括西洛米司特、罗氟司特以及许多其他新的药物实体,其中罗氟司特是第一个获得临床批准用于治疗慢性阻塞性肺疾病(COPD)的同类药物。由于这些物质的可用性,以及不能排除在运动中滥用这些化合物的可能性,因此有必要在运动兴奋剂检测计划中探测这些化合物的流行程度。
采用人肝微粒体孵育生成罗利普兰、罗氟司特和西洛米司特的已知尿液 I 相代谢物。通过液相色谱-高分辨率/高精度串联质谱(LC/MS/MS)研究获得的代谢物,并利用已建立和最相关代谢物的参考产物离子质谱,提供全面兴奋剂控制所需的信息。该分析程序基于常规的兴奋剂常规检测,采用酶水解,随后进行液-液萃取,随后进行 LC/MS/MS 测量。
阐明了目标分析物的诊断产物离子结构和裂解途径,为在现有的常规运动兴奋剂检测测试方法中实施提供了所需的信息。该方法可检测到完整药物的检测限为 1-5ng/mL,进一步的分析特性(日内精密度为 1.5-13.7%,日间精密度为 7.3-18.6%,回收率为 20-100%,离子抑制/增强以及特异性)也得到了确定。此外,还对一名接受罗氟司特治疗的 COPD 患者的尿液样本进行了罗氟司特的概念验证分析。