Literature DB >> 3413033

Variable bioavailability of papaverine.

G Berg1, K A Jönsson, M Hammar, B Norlander.   

Abstract

The plasma concentration curves of papaverine have been studied in nine healthy males and seven patients after administration of single intravenous (80 mg) and oral (80 mg) doses. The bioavailability of the drug was highly variable with a mean of 28% (range 5-99%) but reproducible within the same individual (4 of the volunteers) after a repeated (80 mg) oral dose. The calculated half-life after intravenous administration ranged between 1.2-6.6 hours (mean 3.0). The mean apparent volume of distribution was 3.1 l/kg and the mean total plasma clearance was 836 ml/min. It is concluded that papaverine shows an unacceptable inter-individual variation in the bioavailability after oral administration of 80 mg tablets.

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Year:  1988        PMID: 3413033     DOI: 10.1111/j.1600-0773.1988.tb01893.x

Source DB:  PubMed          Journal:  Pharmacol Toxicol        ISSN: 0901-9928


  2 in total

1.  Pharmacokinetics and bioavailability of drotaverine in humans.

Authors:  O O Bolaji; C O Onyeji; A O Ogundaini; T A Olugbade; F A Ogunbona
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1996 Jul-Sep       Impact factor: 2.441

2.  In Vitro Effects of Papaverine on Cell Proliferation, Reactive Oxygen Species, and Cell Cycle Progression in Cancer Cells.

Authors:  Daniella A Gomes; Anna M Joubert; Michelle H Visagie
Journal:  Molecules       Date:  2021-10-22       Impact factor: 4.411

  2 in total

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