Pharmacokinetics of the oral narcotic analgesic bezitramide and preliminary observations on its effect on experimentally induced pain

Eur J Clin Pharmacol. 1984;27(5):615-8. doi: 10.1007/BF00556902.

Abstract

The oral absorption of bezitramide 5 mg was studied in 7 human volunteers, using a specific radioimmuno-assay which measured both bezitramide and its active metabolite R-4618. A lag time of 0.5-1.0 h and a Cmax of 5.4 ng/ml plasma were found, the latter occurring 2.5-3.5 h after administration. The apparent elimination half-life varied from 11 to 24 h. Less than 0.3% of the dose was excreted unchanged in the urine. High concentrations in the faeces of some individuals indicate incomplete absorption and/or biliary secretion. The analgesic effect, using a standardized superficial electrical stimulation method, reached its maximum between 2.5 and 3.5 h after dosing, in accordance with the absorption phase. The duration of the effect was highly variable. Experiments in rats (n = 6, 3H-bezitramide 2.5 micrograms), demonstrated extensive biliary excretion (up to 70% of total radioactivity) and less than 3% of the label was removed by urinary excretion.

MeSH terms

  • Adult
  • Analgesics / metabolism*
  • Analgesics / therapeutic use
  • Animals
  • Benzimidazoles / metabolism*
  • Benzimidazoles / therapeutic use
  • Bile / metabolism
  • Electric Stimulation
  • Humans
  • Intestinal Absorption
  • Kinetics
  • Male
  • Pain / drug therapy*
  • Rats
  • Rats, Inbred Strains
  • Sensory Thresholds / drug effects

Substances

  • Analgesics
  • Benzimidazoles
  • bezitramide