Absorption of the β-Adrenergic-Blocking Agent, Nadolol, by Mice, Rats, Hamsters, Rabbits, Dogs, Monkeys, and Man: An Unusual Species Difference
- 1 January 1978
- journal article
- research article
- Published by Taylor & Francis in Xenobiotica
- Vol. 8 (8) , 503-508
- https://doi.org/10.3109/00498257809056152
Abstract
1. Dogs absorbed [14C]nadolol almost completely (88-104%) after oral administration of 10-75 mg/kg. In contrast, mice, rats, hamsters, and rabbits, given oral doses of 20 mg/kg, absorbed, at most, 25%. After administration of oral doses of 2-75 mg/kg, monkeys absorbed no more than an average of 30%. Six monkeys given oral doses of 10 mg/kg absorbed 12-44%. 2. In rats, [14C]nadolol was orally absorbed to an average of 13·7-17·5%, whether given in suspension or in solution, indicating that absorption was not limited by rate of dissolution nor by solubility. 3. Mildly hypertensive humans given single doses of [14C]nadolol (2 or 80 mg, orally) and normal subjects given single doses (10 mg, orally) absorbed an average of 20·4-33·3%.This publication has 7 references indexed in Scilit:
- Metabolic Studies in Patients with Nadolol: Oral and Intravenous AdministrationThe Journal of Clinical Pharmacology, 1977
- Problems in Predicting Drug Effects across Species LinesJournal of International Medical Research, 1973
- Recent Developments in Beta Adrenergic Blocking DrugsDrug Metabolism Reviews, 1972
- PHARMACOLOGICAL AND CLINICAL STUDIES WITH TRIACETYL 6-AZAURIDINE1962
- Effect of selective acylation on the oral absorption of a nucleoside by humansBiochemical and Biophysical Research Communications, 1961
- A simple efficient liquid scintillator for counting aqueous solutions in a liquid scintillation counterAnalytical Biochemistry, 1960
- CLINICAL EXPERIENCE WITH ACTINOMYCIN CAnnals of the New York Academy of Sciences, 1960