Pharmacokinetics and pharmacodynamics of intravenous torasemide in diabetic rats induced by alloxan or streptozotocin
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[1] M. Lee,et al. Effects of enzyme inducers and inhibitors on the pharmacokinetics of intravenous torasemide in rats. , 2005, International journal of pharmaceutics.
[2] Ji Young Kim,et al. Dose‐independent pharmacokinetics of torasemide after intravenous and oral administration to rats , 2005, Biopharmaceutics & drug disposition.
[3] J. Kwon,et al. Pharmacokinetic changes of DA-7867, a new oxazolidinone, after intravenous and oral administration to rats with short-term and long-term diabetes mellitus induced by streptozotocin. , 2005, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
[4] So H. Kim,et al. Effect of CYP3A1(23) Induction on Clarithromycin Pharmacokinetics in Rats with Diabetes Mellitus , 2005, Antimicrobial Agents and Chemotherapy.
[5] Y. Choi,et al. Pharmacokinetics and pharmacodynamics of furosemide in protein-calorie malnutrition , 1993, Journal of Pharmacokinetics and Biopharmaceutics.
[6] 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.
[7] M. Gibaldi,et al. Pharmacokinetics of diazepam following multiple-dose oral administration to healthy human subjects , 1977, Journal of Pharmacokinetics and Biopharmaceutics.
[8] Sang -Geon Kim,et al. Effects of cysteine on the pharmacokinetics of intravenous torasemide in rats with protein-calorie malnutrition. , 2004, Journal of pharmaceutical sciences.
[9] Tim Morris,et al. Physiological Parameters in Laboratory Animals and Humans , 1993, Pharmaceutical Research.
[10] So H. Kim,et al. Effects of the rate and composition of fluid replacement on the pharmacokinetics and pharmacodynamics of intravenous torasemide , 2003, The Journal of pharmacy and pharmacology.
[11] E. J. Kim,et al. Pharmacokinetics and pharmacodynamics of intravenous trasemide in mutant nagase aalbuminemic rats , 2003 .
[12] D. Lewis. Guide to Cytochromes P450 : structure and function , 2001 .
[13] Y. Zhang,et al. [Changes of CYP2E1 activity in diabetic rat model]. , 1998, Yao xue xue bao = Acta pharmaceutica Sinica.
[14] So H. Kim,et al. Pharmacokinetics of a new carbapenem, DA‐1131, after intravenous administration to rats with alloxan‐induced diabetes mellitus , 1998, Biopharmaceutics & drug disposition.
[15] E. Mutschler,et al. Clinical Pharmacokinetics and Pharmacodynamics of Torasemide , 1998, Clinical pharmacokinetics.
[16] N. Sugioka,et al. Effect of Glycosylation on Carbamazepine‐Serum Protein Binding in Humans , 1997, Journal of clinical pharmacology.
[17] J. Miners,et al. Human hepatic cytochrome P450 2C9 catalyzes the rate-limiting pathway of torsemide metabolism. , 1995, The Journal of pharmacology and experimental therapeutics.
[18] J. Watkins,et al. Diabetes mellitus-induced alterations of hepatobiliary function. , 1995, Pharmacological reviews.
[19] R. Mehvar. Effect of experimental diabetes mellitus on the pharmacokinetics of atenolol enantiomers in rats. , 1991, Journal of pharmaceutical sciences.
[20] P. Fratino,et al. Serum Protein Binding of Phenytoin and Valproic Acid in Insulin‐Dependent Diabetes Mellitus , 1987, Therapeutic drug monitoring.
[21] J. Watkins,et al. Biliary excretion of organic anions in diabetic rats. , 1986, The Journal of pharmacology and experimental therapeutics.
[22] W. Jusko,et al. Fluid shifts and other factors affecting plasma protein binding of prednisolone by equilibrium dialysis. , 1984, Journal of pharmaceutical sciences.
[23] T. Guentert,et al. Comparison of Equilibrium Times in Dialysis Experiments Using Spiked Plasma or Spiked Buffer , 1982 .
[24] W. L. Chiou. New calculation method of mean total body clearance of drugs and its application to dosage regimens. , 1980, Journal of pharmaceutical sciences.
[25] W. L. Chiou. New calculation method for mean apparent drug volume of distribution and application to rational dosage regimens. , 1979, Journal of pharmaceutical sciences.