Evaluation of Using Dog as an Animal Model to Study the Fraction of Oral Dose Absorbed of 43 Drugs in Humans
- 1 January 2000
- journal article
- research article
- Published by Springer Nature in Pharmaceutical Research
- Vol. 17 (2) , 135-140
- https://doi.org/10.1023/a:1007552927404
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Drug Liposome Partitioning as a Tool for the Prediction of Human Passive Intestinal AbsorptionPharmaceutical Research, 1999
- Linear Correlation of the Fraction of Oral Dose Absorbed of 64 Drugs Between Humans and RatsPharmaceutical Research, 1998
- Absorption and disposition of ranitidine hydrochloride in rat and dogXenobiotica, 1996
- Comparison of the gastrointestinal anatomy, physiology, and biochemistry of humans and commonly used laboratory animalsBiopharmaceutics & Drug Disposition, 1995
- Single dose pharmacokinetics of sumatriptan in healthy volunteersEuropean Journal of Clinical Pharmacology, 1995
- Absorption of iothalamate after oral administration: A preliminary study in humans and interspecies differencesBiopharmaceutics & Drug Disposition, 1987
- Ranitidine bioavailability and kinetics in normal male subjectsClinical Pharmacology & Therapeutics, 1983
- PHARMACOKINETICS AND BIOAVAILABILITY OF ACYCLOVIR IN THE DOG1981
- Pharmacokinetics/pharmacodynamics of furosemide in man: A reviewJournal of Pharmacokinetics and Biopharmaceutics, 1979
- Absorption of the β-Adrenergic-Blocking Agent, Nadolol, by Mice, Rats, Hamsters, Rabbits, Dogs, Monkeys, and Man: An Unusual Species DifferenceXenobiotica, 1978