Effect of sustained release on the pharmacokinetics of valproic acid in the dog
Author:
Publisher
Elsevier BV
Subject
Pharmaceutical Science
Reference24 articles.
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2. Comparative pharmacokinetic analysis of a novel sustained-release dosage form of valproic acid in dog;Bialer;Biopharm. Drug Dispos.,1984
3. Rapid gas Chromatographic assay for plasma monitoring of valpromide and valproic acid;Bialer;J. Pharm. Sci.,1984
4. Valproic acid dosage and plasma protein binding;Bowdle;Clin. Pharmacol. Ther.,1980
5. Valproic acid: review of a new antiepileptic drug;Bruni;Arch. Neurol.,1979
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1. Once‐a‐Day Controlled‐Release Dosage form of Divalproex Sodium I: Formulation Design and in Vitro/in Vivo Investigations;Journal of Pharmaceutical Sciences;2003-06
2. Evaluation of gastrointestinal transit controlled-beagle dog as a suitable animal model for bioavailability testing of sustained-release acetaminophen dosage form;International Journal of Pharmaceutics;1995-05-30
3. Pharmacokinetic Evaluation of Sustained Release Formulations of Antiepileptic Drugs;Clinical Pharmacokinetics;1992-01
4. Comparative pharmacokinetic evaluation of sustained-release theophylline formulations in dogs and humans;International Journal of Pharmaceutics;1987-06
5. Relation between absorption half-life values of four novel sustained-release dosage forms of valproic acid in dogs and human;Biopharmaceutics & Drug Disposition;1986-09
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