Literature DB >> 7224706

Bioavailability of propranolol in the dog.

F L Tse, T M Sanders, J P Reo.   

Abstract

The pharmacokinetics of propranolol in a fasted dog was examined following single oral, intraportal and intravenous doses. Extensive tissue uptake of propranolol occurred after intravenous dosing, the overall distribution volume was 11 liters/kg. Biological half-life was 1.5 hr, but was prolonged after oral and intraportal drug administration. Following oral doses, the absorption efficiency of propranolol as unchanged drug was 71%, while first-pass metabolism accounted for a further loss of 62% prior to its reaching the systemic circulation. Accordingly, the overall oral bioavailability was 27%.

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Year:  1980        PMID: 7224706

Source DB:  PubMed          Journal:  Arch Int Pharmacodyn Ther        ISSN: 0003-9780


  3 in total

1.  Effects of structural modifications on the intestinal permeability of angiotensin II receptor antagonists and the correlation of in vitro, in situ, and in vivo absorption.

Authors:  M D Ribadeneira; B J Aungst; C J Eyermann; S M Huang
Journal:  Pharm Res       Date:  1996-02       Impact factor: 4.200

2.  Applying Biopharmaceutical Classification System (BCS) Criteria to Predict Oral Absorption of Drugs in Dogs: Challenges and Pitfalls.

Authors:  Mark G Papich; Marilyn N Martinez
Journal:  AAPS J       Date:  2015-04-29       Impact factor: 4.009

3.  Hollow fibers as an oral sustained-release delivery system using propranolol hydrochloride.

Authors:  M A Hussain; R C DiLuccio; E Shefter; A R Hurwitz
Journal:  Pharm Res       Date:  1989-12       Impact factor: 4.200

  3 in total

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