Trimoprostil plasma concentration--gastric acid inhibition relationships: potentiation by food

Clin Pharmacol Ther. 1985 Feb;37(2):113-7. doi: 10.1038/clpt.1985.21.

Abstract

A single, oral, 1.5-mg dose of trimoprostil was taken before a standard meal and a matching placebo was taken after a standard meal by 10 subjects (group A). A second group of 10 subjects took placebo before a meal and trimoprostil after the meal (group B), while a third group took placebo both before and after the standard meal (group C). Food-stimulated gastric acid production was measured by intragastric titration for 6.5 hr after dosing. Trimoprostil taken after the meal had a greater effect on gastric acid secretion than when taken before the meal: Duration of effect was 5 to 5.5 hr in group B and 2 to 2.5 hr in group A. Blood samples were drawn and assayed for trimoprostil by gas chromatography-mass spectrometry. Mean trimoprostil plasma concentration and mean inhibition of gastric acid secretion data were fit to two models by the Hill equation. The mean plasma concentration associated with 50% inhibition of gastric acid secretion was 1.25 ng/ml. Trimoprostil plasma concentrations between 3 and 4 ng/ml were associated with 70% to 80% gastric acid inhibition. Overall, there appears to be a pharmacokinetic-pharmacologic correlation between trimoprostil plasma concentrations and inhibition of gastric acid secretion. Trimoprostil (1.5 mg) in the presence of food appears to have a therapeutic advantage, in that it decreases acid secretion longer than when taken without food and suffers no loss of bioavailability.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Anti-Ulcer Agents / blood
  • Anti-Ulcer Agents / metabolism
  • Anti-Ulcer Agents / pharmacology*
  • Biological Availability
  • Dinoprostone* / analogs & derivatives*
  • Double-Blind Method
  • Eating
  • Gastric Acid / metabolism*
  • Humans
  • Kinetics
  • Male
  • Prostaglandins E, Synthetic / blood
  • Prostaglandins E, Synthetic / metabolism
  • Prostaglandins E, Synthetic / pharmacology
  • Random Allocation
  • Time Factors

Substances

  • Anti-Ulcer Agents
  • Prostaglandins E, Synthetic
  • trimoprostil
  • Dinoprostone