Pharmacokinetic study in dogs and monkeys after single intravenous and oral administrations of [14C]-ITF-296

Eur J Drug Metab Pharmacokinet. 1998 Apr-Jun;23(2):239-50. doi: 10.1007/BF03189346.

Abstract

Pharmacokinetics of [14C]-ITF-296 and its metabolites, ITF-1124 and ITF-1577, were studied in dogs and monkeys after a single intravenous (2.5 mg/kg) and oral (10 mg/kg) administration. Radioactivity was measured by LSC while unchanged drug and its metabolites in plasma were assayed by an HPLC-UV method. The absorption of [14C]-ITF-296 after oral administration is practically complete both in dogs and in monkeys. The determination of unchanged drug and its metabolites shows quite a similar profile in dogs and monkeys for ITF-296 and ITF-1124 and a different time-course for ITF-1577. Elimination of radioactivity occurs mainly in urine (namely 70-80%) for both species and the recovery of the dose (higher than 90%) takes place up to 96 h after both treatments.

MeSH terms

  • Absorption
  • Administration, Oral
  • Animals
  • Benzoxazines
  • Carbon Radioisotopes
  • Dogs
  • Injections, Intravenous
  • Ischemia / prevention & control
  • Macaca fascicularis
  • Male
  • Nitrates / blood
  • Nitrates / pharmacokinetics*
  • Oxazines / blood
  • Oxazines / pharmacokinetics*

Substances

  • Benzoxazines
  • Carbon Radioisotopes
  • Nitrates
  • Oxazines
  • sinitrodil