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Pharmacokinetics and bioavailability of oral ifosfamide.

Abstract
The bioavailability of oral N,3-bis(2-chloroethyl) tetrahydro-2H-1,3,2-oxazaphosphorin-2-amine 2-oxide (ifosfamide) (500-mg gelatine capsules) was investigated in 18 patients with bronchogenic carcinoma. Oral and intravenous (Holoxan) ifosfamide was applicated in a randomized sequence on days 1 and 3 at a dose of 1 g/m2 (n = 12) and 2 g/m2 (n = 6). Ifosfamide determination was performed with N/P flame ionization gas chromatography following derivatization with heptafluorobutyric acid. Orally administered ifosfamide showed relatively fast absorption kinetics. Peak levels were reached within 1 h in both dosage groups. With exception of the absorption phase blood level curves of orally and i.v. administered ifosfamide were identical. The average half-life of ifosfamide was 5.5 h (2 g/m2) and 5.8 h (1 g/m2) with a considerable individual variation in both dosage groups. The bioavailability of oral ifosfamide calculated as ration AUCp.o./AUCi.v. was 1.04 after 1 g/m2 ifosfamide and 0.95 in the 6 patients receiving 2 g/m2 ifosfamide. According to our results i.v. administration of ifosfamide especially in fractioned dosage regimes can be replaced by oral application of the same ifosfamide dose.
AuthorsT Wagner, P Drings
JournalArzneimittel-Forschung (Arzneimittelforschung) Vol. 36 Issue 5 Pg. 878-80 (May 1986) ISSN: 0004-4172 [Print] Germany
PMID3730024 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • Ifosfamide
Topics
  • Administration, Oral
  • Adult
  • Aged
  • Biological Availability
  • Female
  • Half-Life
  • Humans
  • Ifosfamide (administration & dosage, adverse effects, metabolism)
  • Kinetics
  • Male
  • Middle Aged

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