Pharmacokinetics and bioavailability of reduced and oxidized N-acetylcysteine

Eur J Clin Pharmacol. 1988;34(1):77-82. doi: 10.1007/BF01061422.

Abstract

The pharmacokinetics and bioavailability of N-acetylcysteine (NAC) have been determined after its intravenous and oral administration to 6 healthy volunteers. According to a randomized cross-over design each subject received NAC 200 mg i.v. and 400 mg p.o., and blood samples were collected for 30 h. Reduced NAC had a volume of distribution (VSS) of 0.59 l.kg-1 and a plasma clearance of 0.84 l.h-1.kg-1. The terminal half-life after intravenous administration was 1.95 h. The oral bioavailability was 4.0%. Based on total NAC concentration, its volume of distribution (VSS) was 0.47 l.kg-1 and its plasma clearance was 0.11 l.h-1.kg-1. The terminal half-life was 5.58 h after intravenous administration and 6.25 h after oral administration. Oral bioavailability of total NAC was 9.1%.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Acetylcysteine / administration & dosage
  • Acetylcysteine / blood
  • Acetylcysteine / metabolism
  • Acetylcysteine / pharmacokinetics*
  • Administration, Oral
  • Adult
  • Biological Availability
  • Drug Administration Schedule
  • Female
  • Half-Life
  • Humans
  • Injections, Intravenous
  • Male
  • Oxidation-Reduction
  • Random Allocation
  • Statistics as Topic
  • Tablets
  • Time Factors

Substances

  • Tablets
  • Acetylcysteine