Synthesis and characterization of membranes obtained by graft copolymerization of 2-hydroxyethyl methacrylate and acrylic acid onto chitosan
Main Author: | |
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Publication Date: | 2006 |
Other Authors: | , , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | https://hdl.handle.net/10316/3795 https://doi.org/10.1016/j.ijpharm.2005.11.019 |
Summary: | Chitosan based membranes to be applied on wound healing as topical drug delivery systems were developed by graft copolymerization of acrylic acid (AA) and 2-hydroxyethyl methacrylate (HEMA) onto chitosan using cerium ammonium nitrate as chemical initiator. Evidence for graft copolymerization of the vinyl monomers onto chitosan was obtained by FTIR and DMTA. Swelling degree, cytotoxicity, thrombogenicity and haemolytic activity of these membranes were evaluated. Chitosan-graft-AA-graft-HEMA showed to be the best matrix for drug delivery systems than chitosan-graft-AA because it retains good swelling properties, but the content in HEMA has improved cytocompatibility, hemocompatibility and thrombogenic character. |
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Synthesis and characterization of membranes obtained by graft copolymerization of 2-hydroxyethyl methacrylate and acrylic acid onto chitosanChitosanAcrylic acid2-Hydroxyethyl methacrylateMembranesWound healingChitosan based membranes to be applied on wound healing as topical drug delivery systems were developed by graft copolymerization of acrylic acid (AA) and 2-hydroxyethyl methacrylate (HEMA) onto chitosan using cerium ammonium nitrate as chemical initiator. Evidence for graft copolymerization of the vinyl monomers onto chitosan was obtained by FTIR and DMTA. Swelling degree, cytotoxicity, thrombogenicity and haemolytic activity of these membranes were evaluated. Chitosan-graft-AA-graft-HEMA showed to be the best matrix for drug delivery systems than chitosan-graft-AA because it retains good swelling properties, but the content in HEMA has improved cytocompatibility, hemocompatibility and thrombogenic character.http://www.sciencedirect.com/science/article/B6T7W-4J2M1S4-1/1/0bac95de859179c9f58b0059043d36fa2006info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttps://hdl.handle.net/10316/3795https://hdl.handle.net/10316/3795https://doi.org/10.1016/j.ijpharm.2005.11.019engInternational Journal of Pharmaceutics. 310:1-2 (2006) 37-45Santos, K. S. C. R. dosCoelho, J. F. J.Ferreira, P.Pinto, I.Lorenzetti, S. G.Ferreira, E. I.Higa, O. Z.Gil, M. H.info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2020-11-06T16:49:07Zoai:estudogeral.uc.pt:10316/3795Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T05:00:58.085077Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Synthesis and characterization of membranes obtained by graft copolymerization of 2-hydroxyethyl methacrylate and acrylic acid onto chitosan |
title |
Synthesis and characterization of membranes obtained by graft copolymerization of 2-hydroxyethyl methacrylate and acrylic acid onto chitosan |
spellingShingle |
Synthesis and characterization of membranes obtained by graft copolymerization of 2-hydroxyethyl methacrylate and acrylic acid onto chitosan Santos, K. S. C. R. dos Chitosan Acrylic acid 2-Hydroxyethyl methacrylate Membranes Wound healing |
title_short |
Synthesis and characterization of membranes obtained by graft copolymerization of 2-hydroxyethyl methacrylate and acrylic acid onto chitosan |
title_full |
Synthesis and characterization of membranes obtained by graft copolymerization of 2-hydroxyethyl methacrylate and acrylic acid onto chitosan |
title_fullStr |
Synthesis and characterization of membranes obtained by graft copolymerization of 2-hydroxyethyl methacrylate and acrylic acid onto chitosan |
title_full_unstemmed |
Synthesis and characterization of membranes obtained by graft copolymerization of 2-hydroxyethyl methacrylate and acrylic acid onto chitosan |
title_sort |
Synthesis and characterization of membranes obtained by graft copolymerization of 2-hydroxyethyl methacrylate and acrylic acid onto chitosan |
author |
Santos, K. S. C. R. dos |
author_facet |
Santos, K. S. C. R. dos Coelho, J. F. J. Ferreira, P. Pinto, I. Lorenzetti, S. G. Ferreira, E. I. Higa, O. Z. Gil, M. H. |
author_role |
author |
author2 |
Coelho, J. F. J. Ferreira, P. Pinto, I. Lorenzetti, S. G. Ferreira, E. I. Higa, O. Z. Gil, M. H. |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Santos, K. S. C. R. dos Coelho, J. F. J. Ferreira, P. Pinto, I. Lorenzetti, S. G. Ferreira, E. I. Higa, O. Z. Gil, M. H. |
dc.subject.por.fl_str_mv |
Chitosan Acrylic acid 2-Hydroxyethyl methacrylate Membranes Wound healing |
topic |
Chitosan Acrylic acid 2-Hydroxyethyl methacrylate Membranes Wound healing |
description |
Chitosan based membranes to be applied on wound healing as topical drug delivery systems were developed by graft copolymerization of acrylic acid (AA) and 2-hydroxyethyl methacrylate (HEMA) onto chitosan using cerium ammonium nitrate as chemical initiator. Evidence for graft copolymerization of the vinyl monomers onto chitosan was obtained by FTIR and DMTA. Swelling degree, cytotoxicity, thrombogenicity and haemolytic activity of these membranes were evaluated. Chitosan-graft-AA-graft-HEMA showed to be the best matrix for drug delivery systems than chitosan-graft-AA because it retains good swelling properties, but the content in HEMA has improved cytocompatibility, hemocompatibility and thrombogenic character. |
publishDate |
2006 |
dc.date.none.fl_str_mv |
2006 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/10316/3795 https://hdl.handle.net/10316/3795 https://doi.org/10.1016/j.ijpharm.2005.11.019 |
url |
https://hdl.handle.net/10316/3795 https://doi.org/10.1016/j.ijpharm.2005.11.019 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
International Journal of Pharmaceutics. 310:1-2 (2006) 37-45 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
aplication/PDF |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
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