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Development of chitosan sponges for buccal administration of insulin
This paper describes the development of a new highly porous, flexible device for buccal peptide administration by a very simple and mild casting/freeze-drying procedure. It consists of a mucoadhesive chitosan layer containing the peptide drug and an impermeable protective layer made of ethylcellulos...
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Published in: | Carbohydrate polymers 2007-04, Vol.68 (4), p.617-625 |
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container_end_page | 625 |
container_issue | 4 |
container_start_page | 617 |
container_title | Carbohydrate polymers |
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creator | Portero, Ana Teijeiro-Osorio, Desirée Alonso, María J. Remuñán-López, Carmen |
description | This paper describes the development of a new highly porous, flexible device for buccal peptide administration by a very simple and mild casting/freeze-drying procedure. It consists of a mucoadhesive chitosan layer containing the peptide drug and an impermeable protective layer made of ethylcellulose. This structure was expected to provide unidirectional drug release to the mucosa and avoid loss of drug due to washout with saliva. Insulin release was modulated by varying some formulation variables (chitosan salt type and
M
w, chitosan solution pH, insulin dose). The main factor affecting insulin release was its diffusion across the matrix, this being related to the water uptake/swelling and dissolution properties of chitosan and the viscosity of the gel formed upon hydration. In addition, an electrostatic interaction could occur between chitosan amino groups and the insulin carboxylic groups. Preliminary mucoadhesion studies showed that the affinity of chitosan sponges to mucin surfaces was related to the swelling and solubility properties of the different salts of chitosan. |
doi_str_mv | 10.1016/j.carbpol.2006.07.028 |
format | article |
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M
w, chitosan solution pH, insulin dose). The main factor affecting insulin release was its diffusion across the matrix, this being related to the water uptake/swelling and dissolution properties of chitosan and the viscosity of the gel formed upon hydration. In addition, an electrostatic interaction could occur between chitosan amino groups and the insulin carboxylic groups. Preliminary mucoadhesion studies showed that the affinity of chitosan sponges to mucin surfaces was related to the swelling and solubility properties of the different salts of chitosan.</description><identifier>ISSN: 0144-8617</identifier><identifier>EISSN: 1879-1344</identifier><identifier>DOI: 10.1016/j.carbpol.2006.07.028</identifier><identifier>CODEN: CAPOD8</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Bilayered drug delivery device ; Biological and medical sciences ; Buccal peptide administration ; Cellulose and derivatives ; Chitosan ; Exact sciences and technology ; General pharmacology ; Insulin ; Medical sciences ; Mucoadhesive sponge ; Natural polymers ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Physicochemistry of polymers ; Starch and polysaccharides</subject><ispartof>Carbohydrate polymers, 2007-04, Vol.68 (4), p.617-625</ispartof><rights>2006 Elsevier Ltd</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-5dcfb5fee56e7de50c838a44044fc02890f376d2d38c5c55e51715cb23017ce93</citedby><cites>FETCH-LOGICAL-c436t-5dcfb5fee56e7de50c838a44044fc02890f376d2d38c5c55e51715cb23017ce93</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=18654252$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Portero, Ana</creatorcontrib><creatorcontrib>Teijeiro-Osorio, Desirée</creatorcontrib><creatorcontrib>Alonso, María J.</creatorcontrib><creatorcontrib>Remuñán-López, Carmen</creatorcontrib><title>Development of chitosan sponges for buccal administration of insulin</title><title>Carbohydrate polymers</title><description>This paper describes the development of a new highly porous, flexible device for buccal peptide administration by a very simple and mild casting/freeze-drying procedure. It consists of a mucoadhesive chitosan layer containing the peptide drug and an impermeable protective layer made of ethylcellulose. This structure was expected to provide unidirectional drug release to the mucosa and avoid loss of drug due to washout with saliva. Insulin release was modulated by varying some formulation variables (chitosan salt type and
M
w, chitosan solution pH, insulin dose). The main factor affecting insulin release was its diffusion across the matrix, this being related to the water uptake/swelling and dissolution properties of chitosan and the viscosity of the gel formed upon hydration. In addition, an electrostatic interaction could occur between chitosan amino groups and the insulin carboxylic groups. Preliminary mucoadhesion studies showed that the affinity of chitosan sponges to mucin surfaces was related to the swelling and solubility properties of the different salts of chitosan.</description><subject>Applied sciences</subject><subject>Bilayered drug delivery device</subject><subject>Biological and medical sciences</subject><subject>Buccal peptide administration</subject><subject>Cellulose and derivatives</subject><subject>Chitosan</subject><subject>Exact sciences and technology</subject><subject>General pharmacology</subject><subject>Insulin</subject><subject>Medical sciences</subject><subject>Mucoadhesive sponge</subject><subject>Natural polymers</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Physicochemistry of polymers</subject><subject>Starch and polysaccharides</subject><issn>0144-8617</issn><issn>1879-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPwzAQhC0EEqXwE5BygVuCHT-SnhBqeUmVuMDZcjZrcJXawU4q8e9J1Uoc2ctevtnZGUKuGS0YZepuU4CJTR-6oqRUFbQqaFmfkBmrq0XOuBCnZEaZEHmtWHVOLlLa0GkUozOyWuEOu9Bv0Q9ZsBl8uSEk47PUB_-JKbMhZs0IYLrMtFvnXRqiGVzwe9r5NHbOX5Iza7qEV8c9Jx9Pj-_Ll3z99vy6fFjnILgactmCbaRFlAqrFiWFmtdGCCqEhenlBbW8Um3Z8hokSImSVUxCU3LKKsAFn5Pbw90-hu8R06C3LgF2nfEYxqRLKjnjrJ5AeQAhhpQiWt1HtzXxRzOq953pjT52pvedaVrp6YFJd3M0MGlKbKPx4NKfuFZSlLKcuPsDh1PancOoEzj0gK2LCINug_vH6RdcSoVI</recordid><startdate>20070401</startdate><enddate>20070401</enddate><creator>Portero, Ana</creator><creator>Teijeiro-Osorio, Desirée</creator><creator>Alonso, María J.</creator><creator>Remuñán-López, Carmen</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20070401</creationdate><title>Development of chitosan sponges for buccal administration of insulin</title><author>Portero, Ana ; Teijeiro-Osorio, Desirée ; Alonso, María J. ; Remuñán-López, Carmen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-5dcfb5fee56e7de50c838a44044fc02890f376d2d38c5c55e51715cb23017ce93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Applied sciences</topic><topic>Bilayered drug delivery device</topic><topic>Biological and medical sciences</topic><topic>Buccal peptide administration</topic><topic>Cellulose and derivatives</topic><topic>Chitosan</topic><topic>Exact sciences and technology</topic><topic>General pharmacology</topic><topic>Insulin</topic><topic>Medical sciences</topic><topic>Mucoadhesive sponge</topic><topic>Natural polymers</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Physicochemistry of polymers</topic><topic>Starch and polysaccharides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Portero, Ana</creatorcontrib><creatorcontrib>Teijeiro-Osorio, Desirée</creatorcontrib><creatorcontrib>Alonso, María J.</creatorcontrib><creatorcontrib>Remuñán-López, Carmen</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Carbohydrate polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Portero, Ana</au><au>Teijeiro-Osorio, Desirée</au><au>Alonso, María J.</au><au>Remuñán-López, Carmen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of chitosan sponges for buccal administration of insulin</atitle><jtitle>Carbohydrate polymers</jtitle><date>2007-04-01</date><risdate>2007</risdate><volume>68</volume><issue>4</issue><spage>617</spage><epage>625</epage><pages>617-625</pages><issn>0144-8617</issn><eissn>1879-1344</eissn><coden>CAPOD8</coden><abstract>This paper describes the development of a new highly porous, flexible device for buccal peptide administration by a very simple and mild casting/freeze-drying procedure. It consists of a mucoadhesive chitosan layer containing the peptide drug and an impermeable protective layer made of ethylcellulose. This structure was expected to provide unidirectional drug release to the mucosa and avoid loss of drug due to washout with saliva. Insulin release was modulated by varying some formulation variables (chitosan salt type and
M
w, chitosan solution pH, insulin dose). The main factor affecting insulin release was its diffusion across the matrix, this being related to the water uptake/swelling and dissolution properties of chitosan and the viscosity of the gel formed upon hydration. In addition, an electrostatic interaction could occur between chitosan amino groups and the insulin carboxylic groups. Preliminary mucoadhesion studies showed that the affinity of chitosan sponges to mucin surfaces was related to the swelling and solubility properties of the different salts of chitosan.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.carbpol.2006.07.028</doi><tpages>9</tpages></addata></record> |
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subjects | Applied sciences Bilayered drug delivery device Biological and medical sciences Buccal peptide administration Cellulose and derivatives Chitosan Exact sciences and technology General pharmacology Insulin Medical sciences Mucoadhesive sponge Natural polymers Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Physicochemistry of polymers Starch and polysaccharides |
title | Development of chitosan sponges for buccal administration of insulin |
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