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Int J Pharm ; 572: 118783, 2019 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-31678393

RESUMO

The purpose of this study was to develop a novel gastroretentive drug delivery system with immediate buoyancy and high wet strength. The proposed bilayer tablet was composed of a drug layer and a highly porous and swellable gastroretentive (GR) layer. The highly porous GR layer was prepared by sublimating the volatile materials after compaction with swellable polymers. This pore-forming process decreased the density of the GR layer and enabled the tablet to float immediately on the dissolution media. The GR layer formulation was optimized by comparing the swelling, erosion, and mechanical properties of candidate swellable polymers. The release rates were conveniently controlled by changing the polymer content in the drug layer, while the swelling and floating properties were provided by the GR layer. The application of percolation theory revealed that the polymer content above the estimated threshold was required for a reliable drug release profile. In vivo study in fed beagle dogs confirmed the enhanced gastric retention time of the tablets compared to that of conventional single layer tablets. Taken together, our data suggest that the proposed system can be a promising platform technology with superior GR properties and a convenient formulation process.


Assuntos
Portadores de Fármacos , Antagonistas dos Receptores H2 da Histamina/administração & dosagem , Polímeros/química , Ranitidina/administração & dosagem , Administração Oral , Animais , Cães , Composição de Medicamentos , Liberação Controlada de Fármacos , Absorção Gástrica , Esvaziamento Gástrico , Antagonistas dos Receptores H2 da Histamina/química , Antagonistas dos Receptores H2 da Histamina/farmacocinética , Masculino , Porosidade , Período Pós-Prandial , Ranitidina/química , Ranitidina/farmacocinética , Solubilidade , Comprimidos
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