The disposition of thioperamide, a histamine H3-receptor antagonist, in rats

J Pharm Pharmacol. 1994 Mar;46(3):209-12. doi: 10.1111/j.2042-7158.1994.tb03780.x.

Abstract

An HPLC method using an ovomucoid-conjugated column has been developed for measurement of thioperamide, a histamine H3 antagonist, with a minimum quantitation limit of 0.05 micrograms mL-1. The assay was used to study the disposition of thioperamide in rats. After bolus intravenous administration of thioperamide (10 mg kg-1), the plasma concentration decreased monoexponentially with a half-life of 26.9 min. The apparent total body clearance of thioperamide from rat plasma was 74.6 mL min-1 kg-1. Although thioperamide was quickly transferred to various tissues, its concentrations in peripheral tissues were higher than that in the brain. However, the brain regional tissue/plasma ratios of thioperamide increased continuously after its injection.

MeSH terms

  • Animals
  • Chromatography, High Pressure Liquid
  • Half-Life
  • Histamine Antagonists*
  • Injections, Intravenous
  • Male
  • Models, Biological
  • Ovomucin / chemistry
  • Piperidines / administration & dosage
  • Piperidines / pharmacokinetics*
  • Rats
  • Rats, Wistar
  • Tissue Distribution

Substances

  • Histamine Antagonists
  • Piperidines
  • Ovomucin
  • thioperamide