Pharmacokinetics of the Monohydroxy Derivative of Oxcarbazepine and Its Enantiomers after a Single Intravenous Dose Given as Racemate Compared with a Single Oral Dose of Oxcarbazepine-Reference-Cited by-同舟云学术

Pharmacokinetics of the Monohydroxy Derivative of Oxcarbazepine and Its Enantiomers after a Single Intravenous Dose Given as Racemate Compared with a Single Oral Dose of Oxcarbazepine

Published:2011-03-09 Issue:6 Volume:39 Page:1103-1110
ISSN:0090-9556
Container-title:Drug Metabolism and Disposition
language:en
Short-container-title:Drug Metab Dispos

Author:

Flesch G.,Czendlik C.,Renard D.,Lloyd P.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmaceutical Science,Pharmacology

Reference11 articles.

1. Mammalian carbonyl reductases;Felsted;Drug Metab Rev,1980

2. Overview of the Clinical Pharmacokinetics of Oxcarbazepine

3. Determination of the R-(−) and S-(+) enantiomers of the monohydroxylated metabolite of oxcarbazepine in human plasma by enantioselective high-performance liquid chromatography

4. Flesch G Czendlik C Ehrhart F Hell F Lloyd P (1999) Pharmacokinetics of the mono-hydroxy derivative of oxcarbazepine and its enantiomers after a single i.v. dose given as racemate compared with a single oral dose of oxcarbazepine. Eur J Pharm Sci Abstr 89 8/2.

5. Gibaldi M Perrier D (1982) Pharmacokinetics. Dekker, New York.

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