Kinetics of medroxalol, a beta- and alpha-adrenoceptor antagonist

Clin Pharmacol Ther. 1983 Dec;34(6):785-91. doi: 10.1038/clpt.1983.250.

Abstract

Eight healthy men received single oral doses of 400, 800, and 1200 mg medroxalol and a single intravenous dose of 1 mg per kg body weight on four occasions separated by at least 2 wk. Plasma medroxalol concentrations were assayed up to 24 hr after each dose by a specific high-pressure liquid chromatographic assay. Urinary excretion of parent compound was determined as well. Following oral doses medroxalol reached peak plasma concentrations within 2.5 to 3 hr. The t 1/2 of the terminal decay phase was 11.1 hr. Mean apparent volume of distribution (aVD) was between 11.2 and 16.4 l/kg, and mean total body clearance (ClT) was between 0.73 and 0.99 l hr-1 kg-1. Mean urinary recovery of parent drug within 48 hr was 2.3%, 3.9%, and 3.6% after the oral doses compared to 8.2% after the intravenous dose. Bioavailability estimated from AUC was 27.2% after 400 mg, 31.3% after 800 mg, and 37.4% after 1200 mg by mouth. Since aVD, t 1/2, ClT, and urinary excretion did not differ significantly after the three oral doses, medroxalol kinetics appear to follow a dose-linear model.

MeSH terms

  • Administration, Oral
  • Adult
  • Biological Availability
  • Ethanolamines / administration & dosage
  • Ethanolamines / metabolism*
  • Humans
  • Injections, Intravenous
  • Kinetics
  • Male
  • Metabolic Clearance Rate

Substances

  • Ethanolamines
  • medroxalol