Pharmacokinetics of DA-8159, a new erectogenic, administered at 10:00 h versus 22:00 h in rats.
暂无分享,去创建一个
Yu C. Kim | J. Kwon | Won Bae Kim | M. Lee | Joo H. Lee
[1] Yu C. Kim,et al. Species differences in the formation of DA-8164 after intravenous and/or oral administration of DA-8159, a new erectogenic, to mice, rats, rabbits, dogs and humans. , 2005, Biopharmaceutics & drug disposition.
[2] Y. Choi,et al. Pharmacokinetics and pharmacodynamics of furosemide in protein-calorie malnutrition , 1993, Journal of Pharmacokinetics and Biopharmaceutics.
[3] W. L. Chiou,et al. Evaluation of potential causes for the incomplete bioavailability of furosemide: Gastric first-pass metabolism , 1983, Journal of Pharmacokinetics and Biopharmaceutics.
[4] W. L. Chiou,et al. Critical evaluation of the potential error in pharmacokinetic studies of using the linear trapezoidal rule method for the calculation of the area under the plasma level-time curve , 1978, Journal of Pharmacokinetics and Biopharmaceutics.
[5] M. Gibaldi,et al. Pharmacokinetics of diazepam following multiple-dose oral administration to healthy human subjects , 1977, Journal of Pharmacokinetics and Biopharmaceutics.
[6] G. Koren,et al. Study on circadian variation in folate pharmacokinetics. , 2005, The Canadian journal of clinical pharmacology = Journal canadien de pharmacologie clinique.
[7] J. Djurhuus,et al. Pharmacokinetics and pharmacodynamics of desmopressin administered orally versus intravenously at daytime versus night-time in healthy men aged 55–70 years , 2004, European Journal of Clinical Pharmacology.
[8] W. B. Kim,et al. Role of human cytochrome P450 3A4 in the metabolism of DA–8159, a new erectogenic , 2004, Xenobiotica; the fate of foreign compounds in biological systems.
[9] A. Nava,et al. Circadian variation of cyclosporine A in renal transplanted patients. , 2004, Revista alergia Mexico.
[10] 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.
[11] 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.
[12] Tetsuro Kato,et al. Chronopharmacokinetics of Tacrolimus in Kidney Transplant Recipients: Occurrence of Acute Rejection , 2003, Journal of clinical pharmacology.
[13] W. Kim,et al. DA-8159, a new PDE5 Iihibitor, induces penile erection in conscious and acute spinal cord injured rabbits. , 2003, European urology.
[14] M. Son,et al. Mechanism of erectogenic effect of the selective phosphodiesterase type 5 inhibitor, DA-8159 , 2002, Archives of pharmacal research.
[15] 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.
[16] Won Bae Kim,et al. In vitro metabolism of a novel phosphodiesterase-5 inhibitor DA-8159 in rat liver preparations using liquid chromatography/electrospray mass spectrometry. , 2002, Biomedical chromatography : BMC.
[17] G. Milano,et al. Clinical pharmacokinetics of 5-fluorouracil with consideration of chronopharmacokinetics , 2002, Chronobiology international.
[18] J. Kwon,et al. Factors influencing the protein binding of a new phosphodiesterase V inhibitor, DA-8159, using an equilibrium dialysis technique. , 2000, Biopharmaceutics & drug disposition.
[19] D. Türck,et al. Steady-state pharmacokinetics of lithium in healthy volunteers receiving concomitant meloxicam. , 2000, British journal of clinical pharmacology.
[20] A. Reinberg. Concepts in chronopharmacology. , 1992, Annual review of pharmacology and toxicology.
[21] B. Hecquet,et al. [Mechanisms and perspectives in clinical chronopharmacokinetics]. , 1989, Therapie.
[22] B. Bruguerolle. [Recent data in chronopharmacokinetics]. , 1987, Pathologie-biologie.
[23] W. Jusko,et al. Fluid shifts and other factors affecting plasma protein binding of prednisolone by equilibrium dialysis. , 1984, Journal of pharmaceutical sciences.
[24] T. Guentert. Time-Dependence in Benzodiazepine Pharmacokinetics Mechanisms and Clinical Significance , 1984, Clinical pharmacokinetics.
[25] A. Reinberg,et al. Circadian Changes of Drug Disposition in Man , 1982, Clinical pharmacokinetics.
[26] T. Guentert,et al. Comparison of Equilibrium Times in Dialysis Experiments Using Spiked Plasma or Spiked Buffer , 1982 .
[27] W. L. Chiou. New calculation method of mean total body clearance of drugs and its application to dosage regimens. , 1980, Journal of pharmaceutical sciences.
[28] W. L. Chiou. New calculation method for mean apparent drug volume of distribution and application to rational dosage regimens. , 1979, Journal of pharmaceutical sciences.