Acitretin (Neotigason). A review of pharmacokinetics and teratogenicity and hypothesis on metabolic pathways

Pharm Weekbl Sci. 1992 Apr 24;14(2):33-7. doi: 10.1007/BF01980479.

Abstract

Acitretin was introduced as a replacement for etretinate, the ethyl ester of acitretin. Acitretin is eliminated at a much faster rate than etretinate. Although both drugs are teratogens, the replacement was important especially as it allowed for a much shorter post-medication period in which pregnancy should be precluded. Recent findings showed the presence of etretinate in the plasma of acitretin-treated patients. This article gives a review of known metabolic pathways of the retinoids and tries to elucidate the possible conversion of acitretin into etretinate after acitretin ingestion.

Publication types

  • Review

MeSH terms

  • Abnormalities, Drug-Induced*
  • Acitretin
  • Animals
  • Biotransformation
  • Etretinate / metabolism
  • Humans
  • Tretinoin / analogs & derivatives*
  • Tretinoin / metabolism
  • Tretinoin / pharmacokinetics
  • Tretinoin / toxicity

Substances

  • Tretinoin
  • Etretinate
  • Acitretin