Metabolic and pharmacokinetic studies following oral administration of 14C-famciclovir to healthy subjects

Xenobiotica. 1994 Apr;24(4):357-68. doi: 10.3109/00498259409045899.

Abstract

1. Following oral administration of 14C-famciclovir (500 mg) to three healthy male subjects, drug-related material was rapidly absorbed as judged by peak plasma concentrations of radioactive material being achieved by 0.75 h (6.7 +/- 0.9 microgram equiv./ml (mean +/- SD). 2. Famciclovir underwent extensive first-pass metabolism and was only detected in the plasma of one subject at low concentrations (0.5 microgram/ml). Famciclovir was rapidly and extensively metabolized to the active antiviral compound penciclovir, which reached peak concentrations in the plasma of 3.6 +/- 0.7 microgram/ml (0.75 h). The plasma elimination half-life value for penciclovir was 2.1 +/- 0.1 h. The 6-deoxy precursor of penciclovir, BRL 42359, was the only other relatively major metabolite detected in plasma. Peak plasma concentrations of BRL 42359 (1.0 +/- 0.1 microgram/ml) were achieved at 0.5 h. 3. After 3 days, 73.0 +/- 6.1% of the radioactive dose was excreted in urine, showing that good absorption of drug-related material occurred. Renal excretion was rapid since 60.2 +/- 4.2 and 72.3 +/- 5.7% of the dose was recovered in the urine samples collected up to 6 and 24 h, respectively. A good recovery of the administered radioactive dose was obtained since a further 26.6 +/- 5.1% of the dose was excreted in the faeces over a 72-h period. 4. Penciclovir and BRL 42359 were the major metabolites detected in urine and faeces. Penciclovir accounted for 59.2 +/- 4.9 and 4.2 +/- 1.4% of the dose in 0-24 h urine and 0-48 h faeces, respectively. Corresponding values for BRL 42359 were 5.0 +/- 0.5 and 17.0 +/- 6.2%, respectively. These metabolites were identified in the biological samples using hplc-ms and ms-ms with thermospray ionization.

MeSH terms

  • 2-Aminopurine / administration & dosage
  • 2-Aminopurine / analogs & derivatives*
  • 2-Aminopurine / metabolism
  • 2-Aminopurine / pharmacokinetics
  • Administration, Oral
  • Adult
  • Antiviral Agents / metabolism*
  • Biotransformation
  • Blood Proteins / metabolism
  • Carbon Radioisotopes
  • Famciclovir
  • Feces
  • Humans
  • Male
  • Metabolic Clearance Rate
  • Middle Aged
  • Prodrugs / administration & dosage
  • Prodrugs / metabolism*
  • Prodrugs / pharmacokinetics
  • Protein Binding
  • Reference Values

Substances

  • Antiviral Agents
  • Blood Proteins
  • Carbon Radioisotopes
  • Prodrugs
  • 2-Aminopurine
  • Famciclovir