Swellable and porous bilayer tablet for gastroretentive drug delivery: Preparation and in vitro-in vivo evaluation

Int J Pharm. 2019 Dec 15:572:118783. doi: 10.1016/j.ijpharm.2019.118783. Epub 2019 Oct 31.

Abstract

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.

Keywords: Floating; Gastric delivery; Percolation; Release kinetics; Sublimation; Swelling.

Publication types

  • Comparative Study

MeSH terms

  • Administration, Oral
  • Animals
  • Dogs
  • Drug Carriers*
  • Drug Compounding
  • Drug Liberation
  • Gastric Absorption
  • Gastric Emptying
  • Histamine H2 Antagonists / administration & dosage*
  • Histamine H2 Antagonists / chemistry
  • Histamine H2 Antagonists / pharmacokinetics
  • Male
  • Polymers / chemistry*
  • Porosity
  • Postprandial Period
  • Ranitidine / administration & dosage*
  • Ranitidine / chemistry
  • Ranitidine / pharmacokinetics
  • Solubility
  • Tablets

Substances

  • Drug Carriers
  • Histamine H2 Antagonists
  • Polymers
  • Tablets
  • Ranitidine