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 |
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container_title | International journal of pharmaceutics |
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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 |
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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 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.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2019.118783</identifier><identifier>PMID: 31678393</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>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</subject><ispartof>International journal of pharmaceutics, 2019-12, Vol.572, p.118783-118783, Article 118783</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-403b5eb5ad35bf48bcec2498f499deec0293d86b13497a9b7048bc13916c8af93</citedby><cites>FETCH-LOGICAL-c365t-403b5eb5ad35bf48bcec2498f499deec0293d86b13497a9b7048bc13916c8af93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378517319308282$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31678393$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Swellable and porous bilayer tablet for gastroretentive drug delivery: Preparation and in vitro-in vivo evaluation</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><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.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Dogs</subject><subject>Drug Carriers</subject><subject>Drug Compounding</subject><subject>Drug Liberation</subject><subject>Floating</subject><subject>Gastric Absorption</subject><subject>Gastric delivery</subject><subject>Gastric Emptying</subject><subject>Histamine H2 Antagonists - administration & dosage</subject><subject>Histamine H2 Antagonists - chemistry</subject><subject>Histamine H2 Antagonists - pharmacokinetics</subject><subject>Male</subject><subject>Percolation</subject><subject>Polymers - chemistry</subject><subject>Porosity</subject><subject>Postprandial Period</subject><subject>Ranitidine - administration & dosage</subject><subject>Ranitidine - chemistry</subject><subject>Ranitidine - pharmacokinetics</subject><subject>Release kinetics</subject><subject>Solubility</subject><subject>Sublimation</subject><subject>Swelling</subject><subject>Tablets</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1v1DAQxS1E1S6lfwLIRy5Z7Dhf5oJQBbRSpSIBZ8sfk-JVNg5jJ9X-9zi7C1dO86T5vRm9R8gbzrac8eb9but30y-N-23JuNxy3rWdeEE2eYpCVG3zkmyYaLui5q24Iq9i3DHGmpKLS3IleJNpKTYEvz_DMGgzANWjo1PAMEdq_KAPgDSti0T7gPRJx4QBIcGY_ALU4fxEHQxZ4-ED_YYwadTJh_F4yI908dlQHMUSKCx6mI_71-Si10OEm_O8Jj-_fP5xe1c8PH69v_30UFjR1KmomDA1mFo7UZu-6owFW1ay6yspHYBlpRSuawwXlWy1NC1bGS4kb2yneymuybvT3QnD7xliUnsf7Zp2hBxSlYJzWdZtKzJan1CLIUaEXk3o9xoPijO11q126ly3WutWp7qz7-35xWz24P65_vabgY8nAHLQxQOqaD2MFpxHsEm54P_z4g-v2ZYw</recordid><startdate>20191215</startdate><enddate>20191215</enddate><creator>Hwang, Kyu-Mok</creator><creator>Nguyen, Thi-Tram</creator><creator>Seok, Su Hyun</creator><creator>Jo, Hyun-Il</creator><creator>Cho, Cheol-Hee</creator><creator>Hwang, Kyu-Min</creator><creator>Kim, Ju-Young</creator><creator>Park, Chun-Woong</creator><creator>Rhee, Yun-Seok</creator><creator>Park, Eun-Seok</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20191215</creationdate><title>Swellable and porous bilayer tablet for gastroretentive drug delivery: Preparation and in vitro-in vivo evaluation</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-403b5eb5ad35bf48bcec2498f499deec0293d86b13497a9b7048bc13916c8af93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Dogs</topic><topic>Drug Carriers</topic><topic>Drug Compounding</topic><topic>Drug Liberation</topic><topic>Floating</topic><topic>Gastric Absorption</topic><topic>Gastric delivery</topic><topic>Gastric Emptying</topic><topic>Histamine H2 Antagonists - administration & dosage</topic><topic>Histamine H2 Antagonists - chemistry</topic><topic>Histamine H2 Antagonists - pharmacokinetics</topic><topic>Male</topic><topic>Percolation</topic><topic>Polymers - chemistry</topic><topic>Porosity</topic><topic>Postprandial Period</topic><topic>Ranitidine - administration & 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. 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.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31678393</pmid><doi>10.1016/j.ijpharm.2019.118783</doi><tpages>1</tpages></addata></record> |
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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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