Pharmacokinetic evaluation of ethionamide suppositories

Pharmacotherapy. 1991;11(5):359-63.

Abstract

The absorption and elimination of ethionamide (ETA) after oral tablets and rectal suppositories were determined in 12 healthy, adult male volunteers. A randomized, double-blind, double-dummy, crossover design was used. Treatments compared 250-mg ETA tablets and a placebo suppository to a 500-mg ETA suppository and two placebo tablets, given 7 days apart. Blood samples were collected at predetermined intervals for 12 hours after the dose. Serum concentrations of ETA were determined using high-performance liquid chromatography. The area under the serum concentration-time curve was used to compare the relative bioavailability of ETA from the two preparations. Relative bioavailability after rectal administration was 57.3% of that after oral administration. The maximum serum concentration after rectal administration was 33% of that after oral administration. Higher doses of ETA and serum concentration monitoring are recommended whenever the suppositories are used.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Administration, Rectal
  • Adolescent
  • Adult
  • Biological Availability
  • Chromatography, High Pressure Liquid
  • Double-Blind Method
  • Ethionamide / administration & dosage
  • Ethionamide / blood
  • Ethionamide / pharmacokinetics*
  • Humans
  • Male
  • Middle Aged
  • Suppositories
  • Tablets

Substances

  • Suppositories
  • Tablets
  • Ethionamide