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Influence of plasticizer type and storage conditions on properties of poly(methyl vinyl ether-co-maleic anhydride) bioadhesive films
Poly(methyl vinyl ether‐co‐maleic anhydride) formed films from aqueous formulations with characteristics that are ideal as a basis for producing a drug‐containing bioadhesive delivery system when plasticized with a monohydroxyl functionalized plasticizer. Hence, films containing a novel plasticizer,...
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Published in: | Journal of applied polymer science 2004-02, Vol.91 (3), p.1576-1589 |
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container_title | Journal of applied polymer science |
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creator | McCarron, Paul A. Woolfson, A. David Donnelly, Ryan F. Andrews, Gavin P. Zawislak, Agnieszka Price, John H. |
description | Poly(methyl vinyl ether‐co‐maleic anhydride) formed films from aqueous formulations with characteristics that are ideal as a basis for producing a drug‐containing bioadhesive delivery system when plasticized with a monohydroxyl functionalized plasticizer. Hence, films containing a novel plasticizer, tripropylene glycol methyl ether (TPME), maintained their adhesive strength and tensile properties when packaged in aluminized foil for extended periods of time. Films plasticized with commonly used polyhydric alcohols, such as the glycerol in this study, underwent an esterification reaction that led to polymer crosslinking, as shown in NMR studies. These revealed the presence of peaks in the ester/carbonyl region, suggesting that glyceride residue formation had been initiated. Given the polyfunctional nature of glycerol, progressive esterification would result in a polyester network and an accompanying profound alteration in the physical characteristics. Indeed, films became brittle over time with a loss of both the aqueous solubility and bioadhesion to porcine skin. In addition, a swelling index was measurable after 7 days, a property not seen with those films containing TPME. This change in bioadhesive strength and pliability was independent of the packaging conditions, rendering the films that contain glycerol as unsuitable as a basis for topical bioadhesive delivery of drug substances. Consequently, films containing TPME have potential as an alternative formulation strategy. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1576–1589, 2004 |
doi_str_mv | 10.1002/app.13228 |
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David ; Donnelly, Ryan F. ; Andrews, Gavin P. ; Zawislak, Agnieszka ; Price, John H.</creator><creatorcontrib>McCarron, Paul A. ; Woolfson, A. David ; Donnelly, Ryan F. ; Andrews, Gavin P. ; Zawislak, Agnieszka ; Price, John H.</creatorcontrib><description>Poly(methyl vinyl ether‐co‐maleic anhydride) formed films from aqueous formulations with characteristics that are ideal as a basis for producing a drug‐containing bioadhesive delivery system when plasticized with a monohydroxyl functionalized plasticizer. Hence, films containing a novel plasticizer, tripropylene glycol methyl ether (TPME), maintained their adhesive strength and tensile properties when packaged in aluminized foil for extended periods of time. Films plasticized with commonly used polyhydric alcohols, such as the glycerol in this study, underwent an esterification reaction that led to polymer crosslinking, as shown in NMR studies. These revealed the presence of peaks in the ester/carbonyl region, suggesting that glyceride residue formation had been initiated. Given the polyfunctional nature of glycerol, progressive esterification would result in a polyester network and an accompanying profound alteration in the physical characteristics. Indeed, films became brittle over time with a loss of both the aqueous solubility and bioadhesion to porcine skin. In addition, a swelling index was measurable after 7 days, a property not seen with those films containing TPME. This change in bioadhesive strength and pliability was independent of the packaging conditions, rendering the films that contain glycerol as unsuitable as a basis for topical bioadhesive delivery of drug substances. Consequently, films containing TPME have potential as an alternative formulation strategy. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1576–1589, 2004</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.13228</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>adhesion ; Applied sciences ; drug delivery systems ; Exact sciences and technology ; glass transition ; Physicochemistry of polymers ; poly(vinyl ethers) ; Polymer industry, paints, wood ; Technology of polymers ; tripropylene glycol methyl ether</subject><ispartof>Journal of applied polymer science, 2004-02, Vol.91 (3), p.1576-1589</ispartof><rights>Copyright © 2003 Wiley Periodicals, Inc.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3358-c415c27f2ae413c84a787e6f8113da848c93677b556c25dc7c6cd13dbfc88ff13</citedby><cites>FETCH-LOGICAL-c3358-c415c27f2ae413c84a787e6f8113da848c93677b556c25dc7c6cd13dbfc88ff13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15595424$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>McCarron, Paul A.</creatorcontrib><creatorcontrib>Woolfson, A. David</creatorcontrib><creatorcontrib>Donnelly, Ryan F.</creatorcontrib><creatorcontrib>Andrews, Gavin P.</creatorcontrib><creatorcontrib>Zawislak, Agnieszka</creatorcontrib><creatorcontrib>Price, John H.</creatorcontrib><title>Influence of plasticizer type and storage conditions on properties of poly(methyl vinyl ether-co-maleic anhydride) bioadhesive films</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>Poly(methyl vinyl ether‐co‐maleic anhydride) formed films from aqueous formulations with characteristics that are ideal as a basis for producing a drug‐containing bioadhesive delivery system when plasticized with a monohydroxyl functionalized plasticizer. Hence, films containing a novel plasticizer, tripropylene glycol methyl ether (TPME), maintained their adhesive strength and tensile properties when packaged in aluminized foil for extended periods of time. Films plasticized with commonly used polyhydric alcohols, such as the glycerol in this study, underwent an esterification reaction that led to polymer crosslinking, as shown in NMR studies. These revealed the presence of peaks in the ester/carbonyl region, suggesting that glyceride residue formation had been initiated. Given the polyfunctional nature of glycerol, progressive esterification would result in a polyester network and an accompanying profound alteration in the physical characteristics. Indeed, films became brittle over time with a loss of both the aqueous solubility and bioadhesion to porcine skin. In addition, a swelling index was measurable after 7 days, a property not seen with those films containing TPME. This change in bioadhesive strength and pliability was independent of the packaging conditions, rendering the films that contain glycerol as unsuitable as a basis for topical bioadhesive delivery of drug substances. Consequently, films containing TPME have potential as an alternative formulation strategy. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1576–1589, 2004</description><subject>adhesion</subject><subject>Applied sciences</subject><subject>drug delivery systems</subject><subject>Exact sciences and technology</subject><subject>glass transition</subject><subject>Physicochemistry of polymers</subject><subject>poly(vinyl ethers)</subject><subject>Polymer industry, paints, wood</subject><subject>Technology of polymers</subject><subject>tripropylene glycol methyl ether</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp1kDtP7DAQRi0EEsuj4B-4QYIiEMdx7JQIsTyEgAIEneWdjFmDN47s8Ag1P_zmspdLRTMz0pzvFB8hOyw_YHleHJquO2C8KNQKmbC8lllZFWqVTMYfy1Rdi3WykdJTnjMm8mpCPs9b61-wBaTB0s6b1DtwHxhpP3RITdvQ1IdoHpFCaBvXu9AmGlraxdBh7B2mr2Dww94C-_ng6atrxzneGDMI2cJ4dDCa5kMTXYP7dOaCaeaY3CtS6_wibZE1a3zC7X97k9xNT26Pz7LL69Pz46PLDDgXKoOSCSikLQyWjIMqjVQSK6sY441RpYKaV1LOhKigEA1IqKAZXzMLSlnL-CbZX3ohhpQiWt1FtzBx0CzXf-vTY336q76R3V2ynUlgvI2mBZd-AkLUoizKkTtccm_O4_C7UB_d3Hybs2XCpR7f_ydMfNaV5FLo-6tT_VBOL674xVRP-R98bpDi</recordid><startdate>20040205</startdate><enddate>20040205</enddate><creator>McCarron, Paul A.</creator><creator>Woolfson, A. 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David ; Donnelly, Ryan F. ; Andrews, Gavin P. ; Zawislak, Agnieszka ; Price, John H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3358-c415c27f2ae413c84a787e6f8113da848c93677b556c25dc7c6cd13dbfc88ff13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>adhesion</topic><topic>Applied sciences</topic><topic>drug delivery systems</topic><topic>Exact sciences and technology</topic><topic>glass transition</topic><topic>Physicochemistry of polymers</topic><topic>poly(vinyl ethers)</topic><topic>Polymer industry, paints, wood</topic><topic>Technology of polymers</topic><topic>tripropylene glycol methyl ether</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McCarron, Paul A.</creatorcontrib><creatorcontrib>Woolfson, A. David</creatorcontrib><creatorcontrib>Donnelly, Ryan F.</creatorcontrib><creatorcontrib>Andrews, Gavin P.</creatorcontrib><creatorcontrib>Zawislak, Agnieszka</creatorcontrib><creatorcontrib>Price, John H.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McCarron, Paul A.</au><au>Woolfson, A. David</au><au>Donnelly, Ryan F.</au><au>Andrews, Gavin P.</au><au>Zawislak, Agnieszka</au><au>Price, John H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of plasticizer type and storage conditions on properties of poly(methyl vinyl ether-co-maleic anhydride) bioadhesive films</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2004-02-05</date><risdate>2004</risdate><volume>91</volume><issue>3</issue><spage>1576</spage><epage>1589</epage><pages>1576-1589</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>Poly(methyl vinyl ether‐co‐maleic anhydride) formed films from aqueous formulations with characteristics that are ideal as a basis for producing a drug‐containing bioadhesive delivery system when plasticized with a monohydroxyl functionalized plasticizer. Hence, films containing a novel plasticizer, tripropylene glycol methyl ether (TPME), maintained their adhesive strength and tensile properties when packaged in aluminized foil for extended periods of time. Films plasticized with commonly used polyhydric alcohols, such as the glycerol in this study, underwent an esterification reaction that led to polymer crosslinking, as shown in NMR studies. These revealed the presence of peaks in the ester/carbonyl region, suggesting that glyceride residue formation had been initiated. Given the polyfunctional nature of glycerol, progressive esterification would result in a polyester network and an accompanying profound alteration in the physical characteristics. Indeed, films became brittle over time with a loss of both the aqueous solubility and bioadhesion to porcine skin. In addition, a swelling index was measurable after 7 days, a property not seen with those films containing TPME. This change in bioadhesive strength and pliability was independent of the packaging conditions, rendering the films that contain glycerol as unsuitable as a basis for topical bioadhesive delivery of drug substances. Consequently, films containing TPME have potential as an alternative formulation strategy. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1576–1589, 2004</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/app.13228</doi><tpages>14</tpages></addata></record> |
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subjects | adhesion Applied sciences drug delivery systems Exact sciences and technology glass transition Physicochemistry of polymers poly(vinyl ethers) Polymer industry, paints, wood Technology of polymers tripropylene glycol methyl ether |
title | Influence of plasticizer type and storage conditions on properties of poly(methyl vinyl ether-co-maleic anhydride) bioadhesive films |
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