Rate-controlled rectal absorption enhancement of cefoxitin by co-administration of sodium salicylate or sodium octanoate in healthy volunteers

Br J Clin Pharmacol. 1989 Jan;27(1):75-81. doi: 10.1111/j.1365-2125.1989.tb05337.x.

Abstract

1. The effects of sodium octanoate and sodium salicylate on the rectal absorption of cefoxitin were investigated in healthy volunteers. Drug solutions were given either as a bolus or as a zero-order infusion. 2. On rectal infusion sodium octanoate and sodium salicylate both enhanced mean cefoxitin bioavailability (+/- s.d.) from 5.0 +/- 1.2% to 9.1 +/- 1.3% and 9.2 +/- 1.5%, respectively. After rectal bolus delivery octanoate increased the mean cefoxitin bioavailability from 7 +/- 3% to 17 +/- 3%, whereas bolus salicylate did not produce a statistically significant effect. All formulations were well tolerated by the volunteers. 3. It is concluded that both octanoate and salicylate are capable of enhancing rectal cefoxitin absorption in man; rate of delivery seems to be an important factor.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Absorption
  • Administration, Rectal
  • Adult
  • Biological Availability
  • Caprylates / administration & dosage*
  • Caprylates / pharmacology
  • Cefoxitin / pharmacokinetics*
  • Drug Synergism
  • Humans
  • Male
  • Rectum / metabolism*
  • Reference Values
  • Sodium Salicylate / administration & dosage*
  • Sodium Salicylate / pharmacology

Substances

  • Caprylates
  • Cefoxitin
  • octanoic acid
  • Sodium Salicylate