Effects of omeprazole or cola beverage on the pharmacokinetics of oral DA-8159, a new erectogenic, in rats.
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J. Kwon | Won Bae Kim | M. Lee | S. Bae | Joo H. Lee
[1] So H. Kim,et al. Interspecies pharmacokinetic scaling of DA‐8159, a new erectogenic, in mice, rats, rabbits and dogs, and prediction of human pharmacokinetics , 2005, Biopharmaceutics & drug disposition.
[2] Yu C. Kim,et al. Effects of enzyme inducers and inhibitors on the pharmacokinetics of intravenous DA‐8159, a new erectogenic, in rats , 2005, Biopharmaceutics & drug disposition.
[3] M. Gibaldi,et al. Pharmacokinetics of diazepam following multiple-dose oral administration to healthy human subjects , 1977, Journal of Pharmacokinetics and Biopharmaceutics.
[4] M. Danhof,et al. Influence of single- and multiple-dose omeprazole treatment on nifedipine pharmacokinetics and effects in healthy subjects , 2004, European Journal of Clinical Pharmacology.
[5] S. Garg,et al. Influence of an acidic beverage (Coca-Cola) on the pharmacokinetics of phenytoin in healthy rabbits. , 2003, Methods and findings in experimental and clinical pharmacology.
[6] G. Ahn,et al. Efficacy of DA-8159, a new PDE5 inhibitor, for inducing penile erection in rabbits with acute spinal cord injury , 2003, International Journal of Impotence Research.
[7] Yu C. Kim,et al. Pharmacokinetics of DA-8159, a new erectogenic, after intravenous and oral administration to rats: hepatic and intestinal first-pass effects. , 2003, Journal of pharmaceutical sciences.
[8] W. Kim,et al. DA-8159, a new PDE5 Iihibitor, induces penile erection in conscious and acute spinal cord injured rabbits. , 2003, European urology.
[9] M. Son,et al. Mechanism of erectogenic effect of the selective phosphodiesterase type 5 inhibitor, DA-8159 , 2002, Archives of pharmacal research.
[10] So H. Kim,et al. Determination of a new phosphodiesterase V inhibitor, DA-8159, in plasma and urine by high-performance liquid chromatography. , 2002, Journal of pharmaceutical and biomedical analysis.
[11] A. Nicoll,et al. Effect of omeprazole‐induced achlorhydria on trefoil peptide expression in the rat stomach , 2001, Journal of gastroenterology and hepatology.
[12] H. S. Lee,et al. Pharmacokinetics, stability, and blood partition of DA-8159, a new phosphodiesterase V inhibitor. , 2000, Research communications in molecular pathology and pharmacology.
[13] S. Sriwiriyajan,et al. Effect of omeprazole on the pharmacokinetics of itraconazole , 1998, European Journal of Clinical Pharmacology.
[14] M. Klausner,et al. Effect of a Cola Beverage on the Bioavailability of Itraconazole in the Presence of H2 Blockers , 1997, Journal of clinical pharmacology.
[15] J. Houston,et al. Selectivity of omeprazole inhibition towards rat liver cytochromes P450. , 1997, Xenobiotica; the fate of foreign compounds in biological systems.
[16] S. Binkley,et al. Interaction of human liver cytochromes P450 in vitro with LY307640, a gastric proton pump inhibitor. , 1996, Pharmacogenetics.
[17] D. Waxman,et al. Characterization of rat and human liver microsomal cytochrome P-450 forms involved in nifedipine oxidation, a prototype for genetic polymorphism in oxidative drug metabolism. , 1986, The Journal of biological chemistry.
[18] W. L. Chiou. New calculation method for mean apparent drug volume of distribution and application to rational dosage regimens. , 1979, Journal of pharmaceutical sciences.