The pharmacokinetics of tiopronin and its principal metabolite (2-mercaptopropionic acid) after oral administration to healthy volunteers

Eur J Clin Pharmacol. 1992;43(1):93-5. doi: 10.1007/BF02280762.

Abstract

We have studied the pharmacokinetics of tiopronin and its principal metabolite, 2-mercaptopropionic acid (2-MPA) in healthy volunteers after the oral administration of 500 mg (2 Acadione tablets), followed by simultaneous assay of the two compounds in plasma over a period of 48 h using a new method (emission of fluorescence after HPLC and post-column derivatization by pyrene-maleimide). The absorption of tiopronin was slow (tmax between 4 and 6 h) and the plasma concentrations subsequently fell biexponentially. The principal metabolite 2-MPA appeared later in the plasma (tmax between 10 and 12 h after a lag-time of 3 h) then disappeared monoexponentially. About 15% of the tiopronin was metabolized to 2-MPA.

MeSH terms

  • Administration, Oral
  • Adult
  • Chromatography, High Pressure Liquid
  • Humans
  • Male
  • Sulfhydryl Compounds / blood*
  • Time Factors
  • Tiopronin / administration & dosage
  • Tiopronin / blood
  • Tiopronin / pharmacokinetics*

Substances

  • Sulfhydryl Compounds
  • Tiopronin
  • thiolactic acid