Preparation of hydroxypropylmethyl cellulose-based porous matrix for gastroretentive delivery of gabapentin using the freeze-drying method
The aims of the present study were to prepare hydroxypropylmethyl cellulose (HPMC)-based porous matrix tablets for gastroretentive drug delivery and to characterize their physicochemical properties. Gabapentin (GBP) was used as a model drug. Paste containing GBP, HPMC and water was molded and freeze...
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Veröffentlicht in: | Cellulose (London) 2013-12, Vol.20 (6), p.3143-3154 |
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creator | Kim, Ju-Young Kim, Sang-hyub Rhee, Yun-Seok Park, Chun-Woong Park, Eun-Seok |
description | The aims of the present study were to prepare hydroxypropylmethyl cellulose (HPMC)-based porous matrix tablets for gastroretentive drug delivery and to characterize their physicochemical properties. Gabapentin (GBP) was used as a model drug. Paste containing GBP, HPMC and water was molded and freeze-dried to prepare freeze-dried gastroretentive matrix tablet (FD-GRT). In vitro drug release and erosion studies were also performed. Although FD-GRT exhibited porous structure, they had good tablet strength and friability. Density of FD-GRT ranged from 0.402 to 0.509 g/cm³ and thus they could float on the medium surface without any lag time. FD-GRT was remained floated until the entire matrix erosion or end of drug release during in vitro release test. Release behavior of GBP could be modulated by the amount and the viscosity grade of HPMC. However, large amount and high viscosity of HPMC caused trouble in molding prior to freeze-drying. Addition of ethylcellulose could retard the release rate of GBP, with relatively low increase in viscosity of paste. Since pores generated by freeze drying imparted buoyancy for gastric retention to FD-GRT, additional materials for buoyancy was not necessary and FD-GRT had no lag time for buoyancy due to low density. Therefore it could be a promising tool for gastroretentive drug delivery. |
doi_str_mv | 10.1007/s10570-013-0048-7 |
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Gabapentin (GBP) was used as a model drug. Paste containing GBP, HPMC and water was molded and freeze-dried to prepare freeze-dried gastroretentive matrix tablet (FD-GRT). In vitro drug release and erosion studies were also performed. Although FD-GRT exhibited porous structure, they had good tablet strength and friability. Density of FD-GRT ranged from 0.402 to 0.509 g/cm³ and thus they could float on the medium surface without any lag time. FD-GRT was remained floated until the entire matrix erosion or end of drug release during in vitro release test. Release behavior of GBP could be modulated by the amount and the viscosity grade of HPMC. However, large amount and high viscosity of HPMC caused trouble in molding prior to freeze-drying. Addition of ethylcellulose could retard the release rate of GBP, with relatively low increase in viscosity of paste. Since pores generated by freeze drying imparted buoyancy for gastric retention to FD-GRT, additional materials for buoyancy was not necessary and FD-GRT had no lag time for buoyancy due to low density. Therefore it could be a promising tool for gastroretentive drug delivery.</description><identifier>ISSN: 0969-0239</identifier><identifier>EISSN: 1572-882X</identifier><identifier>DOI: 10.1007/s10570-013-0048-7</identifier><language>eng</language><publisher>Dordrecht: Springer-Verlag</publisher><subject>Bioorganic Chemistry ; Buoyancy ; Cellulose ; Ceramics ; Chemistry ; Chemistry and Materials Science ; Composites ; Density ; Drug delivery systems ; drugs ; Ethyl cellulose ; Freeze drying ; Friability ; Glass ; In vitro methods and tests ; Lag time ; Natural Materials ; Organic Chemistry ; Original Paper ; Physical Chemistry ; physicochemical properties ; Polymer Sciences ; Porous media ; Sustainable Development ; Tablets ; Viscosity</subject><ispartof>Cellulose (London), 2013-12, Vol.20 (6), p.3143-3154</ispartof><rights>Springer Science+Business Media Dordrecht 2013</rights><rights>Cellulose is a copyright of Springer, (2013). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-22de83ab7ba779e838fd5f33b52b387d1d12387ce4611a53eb3c7fc19cc732b93</citedby><cites>FETCH-LOGICAL-c401t-22de83ab7ba779e838fd5f33b52b387d1d12387ce4611a53eb3c7fc19cc732b93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10570-013-0048-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10570-013-0048-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Kim, Ju-Young</creatorcontrib><creatorcontrib>Kim, Sang-hyub</creatorcontrib><creatorcontrib>Rhee, Yun-Seok</creatorcontrib><creatorcontrib>Park, Chun-Woong</creatorcontrib><creatorcontrib>Park, Eun-Seok</creatorcontrib><title>Preparation of hydroxypropylmethyl cellulose-based porous matrix for gastroretentive delivery of gabapentin using the freeze-drying method</title><title>Cellulose (London)</title><addtitle>Cellulose</addtitle><description>The aims of the present study were to prepare hydroxypropylmethyl cellulose (HPMC)-based porous matrix tablets for gastroretentive drug delivery and to characterize their physicochemical properties. Gabapentin (GBP) was used as a model drug. Paste containing GBP, HPMC and water was molded and freeze-dried to prepare freeze-dried gastroretentive matrix tablet (FD-GRT). In vitro drug release and erosion studies were also performed. Although FD-GRT exhibited porous structure, they had good tablet strength and friability. Density of FD-GRT ranged from 0.402 to 0.509 g/cm³ and thus they could float on the medium surface without any lag time. FD-GRT was remained floated until the entire matrix erosion or end of drug release during in vitro release test. Release behavior of GBP could be modulated by the amount and the viscosity grade of HPMC. However, large amount and high viscosity of HPMC caused trouble in molding prior to freeze-drying. Addition of ethylcellulose could retard the release rate of GBP, with relatively low increase in viscosity of paste. Since pores generated by freeze drying imparted buoyancy for gastric retention to FD-GRT, additional materials for buoyancy was not necessary and FD-GRT had no lag time for buoyancy due to low density. Therefore it could be a promising tool for gastroretentive drug delivery.</description><subject>Bioorganic Chemistry</subject><subject>Buoyancy</subject><subject>Cellulose</subject><subject>Ceramics</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Composites</subject><subject>Density</subject><subject>Drug delivery systems</subject><subject>drugs</subject><subject>Ethyl cellulose</subject><subject>Freeze drying</subject><subject>Friability</subject><subject>Glass</subject><subject>In vitro methods and tests</subject><subject>Lag time</subject><subject>Natural Materials</subject><subject>Organic Chemistry</subject><subject>Original Paper</subject><subject>Physical Chemistry</subject><subject>physicochemical properties</subject><subject>Polymer Sciences</subject><subject>Porous media</subject><subject>Sustainable Development</subject><subject>Tablets</subject><subject>Viscosity</subject><issn>0969-0239</issn><issn>1572-882X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kc1q3TAQhUVpobdpHqCrCrpWqh_7ylqW0D8ItNAGuhOyNfJ18LXckVziPkKeOjIudJfVEcM5Z5hPhLwR_Epwrt8nwWvNGReKcV41TD8jB1FryZpG_npODtwcDeNSmZfkVUp3nHOjpTiQh-8Is0OXhzjRGOhp9Rjv1xnjvI5nyKd1pB2M4zLGBKx1CTydI8Yl0bPLONzTEJH2LmWMCBmmPPwB6mEsguvW2LvWzdt8oksapp7mE9CAAH-BeVy3ybYn-tfkRXBjgst_ekFuP338ef2F3Xz7_PX6ww3rKi4yk9JDo1yrW6e1Kc8m-Doo1dayVY32wgtZtIPqKISrFbSq06ETpuu0kq1RF-Td3luO_L1AyvYuLjiVlVbK2piCqhbFJXZXhzElhGBnHM4OVyu43ZDbHbktyO2G3OqSkXsmFe_UA_5vfir0dg8FF63rcUj29ofkoip_VImG8ycdUtVHoR4BAxyalA</recordid><startdate>20131201</startdate><enddate>20131201</enddate><creator>Kim, Ju-Young</creator><creator>Kim, Sang-hyub</creator><creator>Rhee, Yun-Seok</creator><creator>Park, Chun-Woong</creator><creator>Park, Eun-Seok</creator><general>Springer-Verlag</general><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope></search><sort><creationdate>20131201</creationdate><title>Preparation of hydroxypropylmethyl cellulose-based porous matrix for gastroretentive delivery of gabapentin using the freeze-drying method</title><author>Kim, Ju-Young ; Kim, Sang-hyub ; Rhee, Yun-Seok ; Park, Chun-Woong ; Park, Eun-Seok</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-22de83ab7ba779e838fd5f33b52b387d1d12387ce4611a53eb3c7fc19cc732b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Bioorganic Chemistry</topic><topic>Buoyancy</topic><topic>Cellulose</topic><topic>Ceramics</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Composites</topic><topic>Density</topic><topic>Drug delivery systems</topic><topic>drugs</topic><topic>Ethyl cellulose</topic><topic>Freeze drying</topic><topic>Friability</topic><topic>Glass</topic><topic>In vitro methods and tests</topic><topic>Lag time</topic><topic>Natural Materials</topic><topic>Organic Chemistry</topic><topic>Original Paper</topic><topic>Physical Chemistry</topic><topic>physicochemical properties</topic><topic>Polymer Sciences</topic><topic>Porous media</topic><topic>Sustainable Development</topic><topic>Tablets</topic><topic>Viscosity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Ju-Young</creatorcontrib><creatorcontrib>Kim, Sang-hyub</creatorcontrib><creatorcontrib>Rhee, Yun-Seok</creatorcontrib><creatorcontrib>Park, Chun-Woong</creatorcontrib><creatorcontrib>Park, Eun-Seok</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Cellulose (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Ju-Young</au><au>Kim, Sang-hyub</au><au>Rhee, Yun-Seok</au><au>Park, Chun-Woong</au><au>Park, Eun-Seok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of hydroxypropylmethyl cellulose-based porous matrix for gastroretentive delivery of gabapentin using the freeze-drying method</atitle><jtitle>Cellulose (London)</jtitle><stitle>Cellulose</stitle><date>2013-12-01</date><risdate>2013</risdate><volume>20</volume><issue>6</issue><spage>3143</spage><epage>3154</epage><pages>3143-3154</pages><issn>0969-0239</issn><eissn>1572-882X</eissn><abstract>The aims of the present study were to prepare hydroxypropylmethyl cellulose (HPMC)-based porous matrix tablets for gastroretentive drug delivery and to characterize their physicochemical properties. Gabapentin (GBP) was used as a model drug. Paste containing GBP, HPMC and water was molded and freeze-dried to prepare freeze-dried gastroretentive matrix tablet (FD-GRT). In vitro drug release and erosion studies were also performed. Although FD-GRT exhibited porous structure, they had good tablet strength and friability. Density of FD-GRT ranged from 0.402 to 0.509 g/cm³ and thus they could float on the medium surface without any lag time. FD-GRT was remained floated until the entire matrix erosion or end of drug release during in vitro release test. Release behavior of GBP could be modulated by the amount and the viscosity grade of HPMC. However, large amount and high viscosity of HPMC caused trouble in molding prior to freeze-drying. Addition of ethylcellulose could retard the release rate of GBP, with relatively low increase in viscosity of paste. Since pores generated by freeze drying imparted buoyancy for gastric retention to FD-GRT, additional materials for buoyancy was not necessary and FD-GRT had no lag time for buoyancy due to low density. Therefore it could be a promising tool for gastroretentive drug delivery.</abstract><cop>Dordrecht</cop><pub>Springer-Verlag</pub><doi>10.1007/s10570-013-0048-7</doi><tpages>12</tpages></addata></record> |
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subjects | Bioorganic Chemistry Buoyancy Cellulose Ceramics Chemistry Chemistry and Materials Science Composites Density Drug delivery systems drugs Ethyl cellulose Freeze drying Friability Glass In vitro methods and tests Lag time Natural Materials Organic Chemistry Original Paper Physical Chemistry physicochemical properties Polymer Sciences Porous media Sustainable Development Tablets Viscosity |
title | Preparation of hydroxypropylmethyl cellulose-based porous matrix for gastroretentive delivery of gabapentin using the freeze-drying method |
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