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Development of starch/chitosan expandable films as a gastroretentive carrier for ginger extract-loaded solid dispersion
Authors:Kanidta Kaewkroek  Arpa Petchsomrit  Abdi Wira Septama  Ruedeekorn Wiwattanapatapee
Affiliation:1. Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand;2. Faculty of Integrative Medicine, Rajamangala University of Technology Thanyaburi, Thanyaburi, Pathum Thani 12130, Thailand;3. Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Burapha University, Bangsaen, Muang, Chonburi 20131, Thailand;4. Research Center for Chemistry, National Research and Innovation Agency (BRIN), Kawasan Puspiptek Serpong, Tangerang Selatan, Banten 15314, Indonesia;5. Phytomedicine and Pharmaceutical Biotechnology Excellence Research Center, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand
Abstract:Gastroretentive expandable films were developed to provide controlled release of ginger extract (GE) for treatment of gastric diseases. The dosage form consisted of ginger extract solid dispersion (GE-SD) loaded in a starch/chitosan composite film, which was subsequently folded and inserted into a hard gelatin capsule. GE-SD was prepared by solvent evaporation using an optimum weight ratio of 1:1 for GE and PVP K30. Expandable films containing GE-SD were prepared by solvent casting combinations of chitosan and either rice-, glutinous rice - or pregelatinized maize starch with glycerin incorporated as a plasticizer. The optimized film formulation prepared from glutinous rice starch, exhibited tensile strength of 5.4 N/cm2 and high expansion in simulated gastric fluid (SGF), resulting in a 2.8-fold increase in area. The films resulted in sustained release of up to 90% of the content of 6-gingerol during 8 h exposure to SGF. Furthermore, the 6-gingerol released from the film displayed dose-dependent cytotoxic activity against AGS human gastric adenocarcinoma cells and anti-inflammatory activity by inhibiting the production of nitric oxide (NO) in LPS-stimulated RAW264.7 cells.
Keywords:Ginger extract  Solid dispersions  Starch  Chitosan  Expandable film  Gastroretentive drug delivery systems
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