Geboers Sophie, Stappaerts Jef, Mols Raf, Snoeys Jan, Tack Jan, Annaert Pieter, Augustijns Patrick
Drug Delivery and Disposition, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Pharmacokinetics, Dynamics and Metabolism, Janssen Research and Development, Beerse, Belgium.
J Pharm Sci. 2016 Sep;105(9):2974-2981. doi: 10.1016/j.xphs.2016.03.008. Epub 2016 Apr 7.
To relate the reported positive effect of food on the oral bioavailability of abiraterone to the intraluminal behavior of abiraterone acetate, an in vivo experiment was performed, in which duodenal fluids and plasma samples were collected from healthy volunteers after the administration of abiraterone acetate in fasted and postprandial conditions. The plasma concentration-time profiles confirmed the positive food effect. Nevertheless, intraduodenal concentrations of abiraterone acetate and abiraterone did not fully reflect this observation. This apparent discrepancy was explored by performing several in vitro experiments including solubility, dissolution, and transfer studies. Gastrointestinal transfer studies illustrated a positive impact of gastric processing of the abiraterone acetate formulation on the duodenal concentrations in the fasted state, which could not be observed in the postprandial condition. As the influence of gastric dissolution on the intraluminal concentrations in the small intestine declines aborally, it is most likely the superior solubility of abiraterone acetate and abiraterone in intestinal fluids of the fed state that dictates the food effect. Furthermore, N-oxide abiraterone sulfate and abiraterone sulfate appeared in the duodenum at significantly later time points than abiraterone, suggesting biliary excretion of these abiraterone metabolites; this was confirmed by in situ biliary excretion experiments in rats.
为了将所报道的食物对阿比特龙口服生物利用度的积极影响与醋酸阿比特龙的肠腔内行为联系起来,进行了一项体内实验,在禁食和餐后条件下给健康志愿者服用醋酸阿比特龙后,收集十二指肠液和血浆样本。血浆浓度-时间曲线证实了食物的积极影响。然而,醋酸阿比特龙和阿比特龙在十二指肠内的浓度并未完全反映这一观察结果。通过进行包括溶解度、溶出度和转运研究在内的多项体外实验,探讨了这种明显的差异。胃肠道转运研究表明,醋酸阿比特龙制剂的胃部处理对禁食状态下十二指肠内的浓度有积极影响,而在餐后状态下未观察到这种影响。由于胃部溶出对小肠内肠腔浓度的影响在向口侧下降,最有可能是醋酸阿比特龙和阿比特龙在进食状态下肠液中的较高溶解度决定了食物效应。此外,硫酸阿比特龙N-氧化物和硫酸阿比特龙在十二指肠中出现的时间点明显晚于阿比特龙,提示这些阿比特龙代谢产物经胆汁排泄;大鼠原位胆汁排泄实验证实了这一点。