Some factors influencing the in vitro release of phenytoin from formulations

Author:

Bastami S.M.,Groves M.J.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference25 articles.

1. Bioavailability of diphenylhydantoin;Albert;Clin. Pharmacol. Ther.,1974

2. Biological avail ability — a comparison of three phenytoin preparations;Alvan;Lakartidningen,1975

3. Blood phenytoin concentrations produced by ingestion of three different phenytoin preparations;Appleton;Med. J. Aust.,1972

4. The rate of decline of diphenylhydantoin in human plasma;Arnold;Clin. Pharmacol. Ther.,1970

5. Absorption and dissolution studies on sodium diphenylhydantoin capsules;Arnold;Can. J. Pharm. Sci.,1970

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1. Quantitative estimation of phenytoin sodium disproportionation in the formulations using vibration spectroscopies and multivariate methodologies;International Journal of Pharmaceutics;2018-03

2. References;Handbook of Aqueous Solubility Data, Second Edition;2010-04-26

3. References;Handbook of Aqueous Solubility Data, Second Edition;2010-04-26

4. Drug–excipient interactions and their affect on absorption;Pharmaceutical Science & Technology Today;2000-10

5. Assessment of a hydroalcoholic surfactant solution as a medium for the dissolution testing of phenytoin;International Journal of Pharmaceutics;1996-08

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