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用于兴奋剂控制的选择性雄激素受体调节剂 LGD-3303 的马体内代谢产物分析。

Equine in vivo metabolite profiling of the selective androgen receptor modulator LGD-3303 for doping control.

机构信息

Department of Medicinal Chemistry, Uppsala University, Box 574, 75123 Uppsala Sweden.

Kenneth L. Maddy Equine Analytical Pharmacology Laboratory, School of Veterinary Medicine, University of California, Davis, CA 95616, USA.

出版信息

J Pharm Biomed Anal. 2023 Sep 5;233:115468. doi: 10.1016/j.jpba.2023.115468. Epub 2023 May 18.

Abstract

LGD-3303 is a Selective Androgen Receptor Modulator (SARM) that is prohibited in both equine and human sports due to its anabolic properties. The aim of this study was to investigate the equine in vivo metabolite profile of LGD-3303 and identify drug metabolites that can be suitable as new and improved analytical targets for equine doping control. This was performed by an oral administration of 0.05 mg·kg LGD-3303 to horses, where blood and urine samples were collected up to 96 h after administration. The in vivo samples consisting of plasma, urine and hydrolyzed urine were analyzed utilizing ultra-high performance liquid chromatography hyphenated to a Q Exactive™ Orbitrap™ high resolution mass spectrometer with a heated electrospray ionization source. A total of eight metabolites of LGD-3303 were tentatively identified, including one carboxylated and several hydroxylated metabolites in combination with glucuronic acid conjugates. A monohydroxylated metabolite is suggested as an analytical target for doping control analysis of plasma and urine after hydrolysis with β-glucuronidase, due to the high intensity and prolonged detection time in comparison to parent LGD-3303.

摘要

LGD-3303 是一种选择性雄激素受体调节剂 (SARM),由于其具有同化作用,已在赛马和人类运动中被禁用。本研究旨在调查 LGD-3303 在马体内的代谢物特征,并确定可作为赛马兴奋剂控制新的和改进的分析靶标的药物代谢物。这是通过给马口服 0.05mg·kg LGD-3303 来实现的,在给药后 96 小时内采集血液和尿液样本。体内样本包括血浆、尿液和水解尿液,利用超高效液相色谱-串联 Q Exactive™ Orbitrap™高分辨率质谱仪,结合加热电喷雾电离源进行分析。共鉴定出 LGD-3303 的八种代谢物,包括一个羧化代谢物和几个与葡萄糖醛酸缀合的羟基化代谢物。由于与母体 LGD-3303 相比,强度更高且检测时间更长,因此在水解后用β-葡萄糖醛酸苷酶对血浆和尿液进行兴奋剂控制分析时,建议使用单羟基化代谢物作为分析靶标。

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