Pharmacokinetics of pyrimethamine in healthy young volunteers using a new solid phase extraction/HPLC method

Eur J Drug Metab Pharmacokinet. 1991:Spec No 3:284-90.

Abstract

The single dose pharmacokinetics of pyrimethamine were determined in 12 healthy young volunteers using a newly developed fully automated analytical system which combines liquid solid extraction on disposable extraction columns and high performance liquid chromatography. This technique is highly sensitive (detection 1 ng/ml) and reproducible. Following a 50mg dose of the drug, the plasma concentration peaked at 0.48 0.13 g/ml (msd) and was attained 2.5 hours (median value) post dosing. Thereafter, the plasma level of pyrimethamine decreased slowly, the level at 336 hours after administration being still about 40 ng/ml. The area under the plasma concentration-time curve (AUC0-inf) was 56.8 18.4 h.mg/ml. The volume of distribution Vd was: 2.42 1.25 l/kg and the total clearance: 15.55 4.48 ml/h/kg. Urinary excretion represented about 20% to 40% of the dose after seven days of the administered dose.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Biological Availability
  • Chromatography, High Pressure Liquid
  • Female
  • Humans
  • Indicators and Reagents
  • Male
  • Pyrimethamine / administration & dosage
  • Pyrimethamine / pharmacokinetics*
  • Spectrophotometry, Ultraviolet
  • Tablets

Substances

  • Indicators and Reagents
  • Tablets
  • Pyrimethamine