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Dissolution properties of controlled release capsules containing quetiapine fumarate

  • Pil Yun Kim
  • , Jun Jae Jung
  • , Nam Yeong Kim
  • , Jin Woo Kim
  • , Jeong Min Choi
  • , Won Chan Lee
  • , Jeong Eun Song
  • , Gilson Khang*
  • *Corresponding author for this work
  • Jeonbuk National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Quetiapine fumarate (QF) is a BCS CLASS II with low solubility and high permeability, which has a problem of low bioavailability. It has also been reported that Quetiapine possesses two hydroxyl groups, so it has a higher solubility under acidic conditions. The solubility is low in the range of pH 4 or higher and it is high when pH is 2, and it decreases when the pH is lower than 2 which is due to ion effect. Therefore, capsules were prepared using immediate-release and sustained-release granules to improve the solubility of QF and induce constant release even with a change in pH. XRD and DSC were used to evaluate the crystallinity and inclusion of drugs, SEM was used for morphological analysis, and FTIR was used to analyze chemical changes. In addition, fluidity was evaluated to confirm that it was improved by granulation process. Finally, the solubility patterns of solid dispersions and capsules were analyzed by a solubility test.

Original languageEnglish
Pages (from-to)715-724
Number of pages10
JournalPolymer (Korea)
Volume44
Issue number5
DOIs
StatePublished - 2020.09

Keywords

  • Controlled release
  • Immediate release
  • Quetiapine fumarate
  • Rotary evaporation
  • Spray dry solid dispersion
  • Sustained release

Quacquarelli Symonds(QS) Subject Topics

  • Materials Science
  • Engineering - Chemical

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