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

[Display omitted] 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...

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Veröffentlicht in:International journal of pharmaceutics 2019-12, Vol.572, p.118783-118783, Article 118783
Hauptverfasser: Hwang, Kyu-Mok, Nguyen, Thi-Tram, Seok, Su Hyun, Jo, Hyun-Il, Cho, Cheol-Hee, Hwang, Kyu-Min, Kim, Ju-Young, Park, Chun-Woong, Rhee, Yun-Seok, Park, Eun-Seok
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container_title International journal of pharmaceutics
container_volume 572
creator Hwang, Kyu-Mok
Nguyen, Thi-Tram
Seok, Su Hyun
Jo, Hyun-Il
Cho, Cheol-Hee
Hwang, Kyu-Min
Kim, Ju-Young
Park, Chun-Woong
Rhee, Yun-Seok
Park, Eun-Seok
description [Display omitted] 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.
doi_str_mv 10.1016/j.ijpharm.2019.118783
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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. 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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. 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dosage</topic><topic>Ranitidine - chemistry</topic><topic>Ranitidine - pharmacokinetics</topic><topic>Release kinetics</topic><topic>Solubility</topic><topic>Sublimation</topic><topic>Swelling</topic><topic>Tablets</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hwang, Kyu-Mok</creatorcontrib><creatorcontrib>Nguyen, Thi-Tram</creatorcontrib><creatorcontrib>Seok, Su Hyun</creatorcontrib><creatorcontrib>Jo, Hyun-Il</creatorcontrib><creatorcontrib>Cho, Cheol-Hee</creatorcontrib><creatorcontrib>Hwang, Kyu-Min</creatorcontrib><creatorcontrib>Kim, Ju-Young</creatorcontrib><creatorcontrib>Park, Chun-Woong</creatorcontrib><creatorcontrib>Rhee, Yun-Seok</creatorcontrib><creatorcontrib>Park, Eun-Seok</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hwang, Kyu-Mok</au><au>Nguyen, Thi-Tram</au><au>Seok, Su Hyun</au><au>Jo, Hyun-Il</au><au>Cho, Cheol-Hee</au><au>Hwang, Kyu-Min</au><au>Kim, Ju-Young</au><au>Park, Chun-Woong</au><au>Rhee, Yun-Seok</au><au>Park, Eun-Seok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Swellable and porous bilayer tablet for gastroretentive drug delivery: Preparation and in vitro-in vivo evaluation</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2019-12-15</date><risdate>2019</risdate><volume>572</volume><spage>118783</spage><epage>118783</epage><pages>118783-118783</pages><artnum>118783</artnum><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted] The purpose of this study was to develop a novel gastroretentive drug delivery system with immediate buoyancy and high wet strength. 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ispartof International journal of pharmaceutics, 2019-12, Vol.572, p.118783-118783, Article 118783
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subjects Administration, Oral
Animals
Dogs
Drug Carriers
Drug Compounding
Drug Liberation
Floating
Gastric Absorption
Gastric delivery
Gastric Emptying
Histamine H2 Antagonists - administration & dosage
Histamine H2 Antagonists - chemistry
Histamine H2 Antagonists - pharmacokinetics
Male
Percolation
Polymers - chemistry
Porosity
Postprandial Period
Ranitidine - administration & dosage
Ranitidine - chemistry
Ranitidine - pharmacokinetics
Release kinetics
Solubility
Sublimation
Swelling
Tablets
title Swellable and porous bilayer tablet for gastroretentive drug delivery: Preparation and in vitro-in vivo evaluation
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