Preparation and in-vitro evaluation of sustained release phenytoin sodium matrix tablets prepared by co-evaporation method using different polymers

Roohullah, Zafar Iqbal, Fazli Nasir, Muhammad Akhlaq, Sajid Khan Sadozai, Ibrahim Khadra, Shahida Zakir

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1 Citation (Scopus)

Abstract

Sustained-release matrix tablets of Phenytoin sodium was developed and evaluated. Tablets were prepared by co-evaporation method using hydroxy propyl methyl cellulose (HPMC), carboxymethyl cellulose (CMC) and polyvinylpyrrolidon-K90 (PVP-K90), the hydrophilic polymers as release sustaining materials. Formulations were designed using drug to polymers ratio 1:1, 1:1.5, 1:2 with the aim to develop twice daily sustained release matrix tablets. Physical characterization of both granules and tablets were evaluated. USP dissolution apparatus I was used for the In-vitro drug release study of the tablets. Drug release data was evaluated using various models like Zero-order, First-order, Higuchi model, Korsmeyer model and Hixson-Crowell model. The resulting matrix tablets prepared with all the polymers used in drug to polymer ratio fulfilled all the official requirements for a tablet dosage form except dissolution, while HPMC with drug to polymer ratio 1:2 extend the release of the drug up to 12 hours.

Original languageEnglish
Pages (from-to)246-252
Number of pages7
JournalMiddle East Journal of Scientific Research
Volume11
Issue number2
Publication statusPublished - 16 May 2012

Keywords

  • co-evaporation method
  • hydrophilic polymers (HPMC, CMC and PVP)
  • phenytoin sodium tablets
  • sustained release

Cite this

Roohullah, Iqbal, Z., Nasir, F., Akhlaq, M., Sadozai, S. K., Khadra, I., & Zakir, S. (2012). Preparation and in-vitro evaluation of sustained release phenytoin sodium matrix tablets prepared by co-evaporation method using different polymers. Middle East Journal of Scientific Research, 11(2), 246-252.