作者: Young H. Choi , Young S. Lee , Soo H. Bae , Tae K. Kim , Bong-Y. Lee
DOI: 10.1002/BDD.669
关键词:
摘要: The pharmacokinetics of mirodenafil and its two metabolites, SK3541 SK3544, after intravenous (5, 10, 20 50 mg/kg) oral (10, administration mirodenafil, the first-pass effect intravenous, oral, intraportal, intragastric intraduodenal (20 were evaluated in rats. dose-dependent both due to saturable hepatic metabolism mirodenafil. After approximately 2.59% dose was not absorbed, F value 29.4%, gastrointestinal effects 21.4% 54.3% dose, respectively. low rats mainly considerable equilibrium plasma-to-blood cell partition ratios independent initial blood concentrations 1-10 microg/ml; mean values 1.08-1.21. plasma binding rat 87.8%.