In vitro and in vivo metabolism and pharmacokinetics of bis [(t-butyl)-S-acyl-2-thioethyl]-beta-L-2',3'-dideoxy-5-fluorocytidine monophosphate

Nucleosides Nucleotides Nucleic Acids. 2000 Jan-Feb;19(1-2):481-99. doi: 10.1080/15257770008033023.

Abstract

Exposure to 10 &M L-FddCMP-bisSATE led to formation of intracellular L-FddCTP levels of 410.1(+/-) +/- 46.2 and 242.1 +/- 13.2 pmol/10(6) cells in unstimulated and PHAstimulated PBM cells, respectively; whereas, exposure of cells to the parent nucleoside, L-FddC, generated 5-10-fold less L-FddCTP. In Hep-G2 cells and EGF/HGF stimulated and unstimulated primary cultured hepatocytes, the active metabolite reached 113 +/- 29, 23.9 +/- 15.6, and 20.6 +/- 10.5 pmol/10(6) cells. Three other metabolites, L-FddCMP-monoSATE, L-FddCMP-SH, and M I, were detected intracellularly and extracellularly in all cell types examined. Intravenous administered dose of 3 mg/kg L-FddCMP-bisSATE to rhesus monkeys resulted in plasma concentration levels of 2.06 +/- 1.00 and 0.39 +/- 0.15 &M of L-FddCMP-monoSATE and L-FddC, respectively, while the prodrug was completely cleared metabolically within 15 min. Following oral administration of an equivalent dose, the absolute oral bioavailability of L-FddC derived from L-FddCMP-bisSATE administration was 65%.

MeSH terms

  • Administration, Oral
  • Animals
  • Antiviral Agents / chemical synthesis
  • Antiviral Agents / pharmacokinetics*
  • Antiviral Agents / pharmacology
  • Antiviral Agents / urine
  • Biological Availability
  • Cells, Cultured
  • Chromatography, High Pressure Liquid
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / chemical synthesis
  • Deoxycytidine / pharmacokinetics
  • Deoxycytidine / pharmacology
  • Deoxycytidine / urine
  • Drug Stability
  • Female
  • Humans
  • Leukocytes, Mononuclear / metabolism
  • Liver / cytology
  • Macaca mulatta
  • Phosphorylation

Substances

  • Antiviral Agents
  • FddCMP-bisSate
  • Deoxycytidine