Dib Josef, Tretzel Laura, Piper Thomas, Lagojda Andreas, Kuehne Dirk, Schänzer Wilhelm, Thevis Mario
Center for Preventive Doping Research - Institute of Biochemistry, German Sport University Cologne, Am Sportpark Müngersdorf 6, 50933 Cologne, Germany.
Bayer AG, Crop Science Division, Alfred-Nobel-Str. 50, 40789 Monheim, Germany.
Clin Mass Spectrom. 2017 Oct 28;6:13-20. doi: 10.1016/j.clinms.2017.10.002. eCollection 2017 Dec.
AdipoRon and 112254 represent two known synthetic adiponectin receptor (adipoR) agonists. Although AdipoRon is the more potent compound, both have physiological properties that are similar to adiponectin - an adipokine with antidiabetic and antiatherogenic effects. Several transcriptional regulators are activated by adipoR-agonists leading to increased mitochondrial DNA content , an effect that can be abused by athletes for performance enhancing purposes. In the context of preventive anti-doping research, detection of AdipoRon and 112254 in routine doping control specimens would be valuable. Here, we describe our process for incorporating AdipoRon and 112254 into routine doping control methods involving urine and dried blood spot (DBS) analysis. Method validation including evaluation of specificity, limit of detection, identification capability, carryover, matrix interference, recovery, interday and intraday precision and linearity to standards provided by WADA. For identification in human urine, a liquid chromatography-tandem mass spectrometry-based testing approach was implemented for both adipoR agonists and two respective phase-I metabolites. Recovery of 85-104%, satisfactory limits of detection (i.e., 0.5-1 ng/mL), and imprecision values over three days at three concentration levels of <19% demonstrated the assay's fitness-for-purpose. For identification from DBS a liquid chromatography-high-resolution/high-accuracy tandem mass spectrometry with online solid-phase extraction was implemented for AdipoRon and 112254. Here also, acceptable recoveries (i.e., 22-33%), limits of detection of 5-10 ng/mL, and imprecision values over three days at three concentration levels of <23%, were demonstrated. Hence, two methods for doping control screening from urine and DBS were established and shown to be fit-for-purpose for routine use.
AdipoRon和112254是两种已知的合成脂联素受体(adipoR)激动剂。尽管AdipoRon是更有效的化合物,但两者都具有与脂联素相似的生理特性,脂联素是一种具有抗糖尿病和抗动脉粥样硬化作用的脂肪因子。几种转录调节因子被adipoR激动剂激活,导致线粒体DNA含量增加,运动员可能会滥用这种作用来提高成绩。在预防性反兴奋剂研究的背景下,在常规兴奋剂检测样本中检测AdipoRon和112254将很有价值。在此,我们描述了将AdipoRon和112254纳入涉及尿液和干血斑(DBS)分析的常规兴奋剂检测方法的过程。方法验证包括对特异性、检测限、识别能力、残留、基质干扰、回收率、日间和日内精密度以及符合世界反兴奋剂机构(WADA)提供标准的线性进行评估。为了在人尿中进行识别,对两种adipoR激动剂及其两种相应的I期代谢物都采用了基于液相色谱-串联质谱的检测方法。回收率为85%-104%,检测限令人满意(即0.5-1 ng/mL),在三个浓度水平下三天的不精密度值<19%,证明了该检测方法的适用性。为了从DBS中进行识别,对AdipoRon和112254采用了在线固相萃取的液相色谱-高分辨率/高精度串联质谱法。在此同样证明了可接受的回收率(即22%-33%)、检测限为5-10 ng/mL,以及在三个浓度水平下三天的不精密度值<23%。因此,建立了两种从尿液和DBS中进行兴奋剂检测筛查的方法,并证明适用于常规使用。