Preparation and Characterization of Chitosan/mPEG-PCL Blended Membranes for Wound Dressing and Controlled Gentamicin Release
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1590/1980-5373-MR-2017-0951 http://hdl.handle.net/11449/160551 |
Resumo: | In this paper, a novel wound dressing membrane for controlled release of gentamicin (GE), while covering and protecting the wound was investigated. Chitosan (CHI) was associated with methoxy polyethylene glycol - polycaprolactone copolymer (mPEG-PCL) to prepare the blended wound dressing membranes. The use of copolymer mPEG-PCL was necessary to improve the compatibility between CHI and PCL. The association of CHI and PCL was required to control the water retention and release rate of encapsulated GE. In vitro release studies were performed with the mPEG-PCL/ CHI-GE membranes in order to evaluate the effect of copolymer concentration on the kinetics of GE release and water uptake. Reduced burst release rates and swelling ratios were observed for the 1/2 and 1/4 mPEG-PCL/CHI-GE membranes. In addition, all gentamicin-loaded membranes inhibited S. aureus and E. coli growth, and demonstrated color, moisture and thermal stability. Therefore, mPEG-PCL/CHI-GE membranes showed important features for potential wound dressing and drug delivery applications. |
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Preparation and Characterization of Chitosan/mPEG-PCL Blended Membranes for Wound Dressing and Controlled Gentamicin ReleaseCopolymerblendmethoxy polyethylene glycolpolycaprolactoneantibioticdrug deliveryIn this paper, a novel wound dressing membrane for controlled release of gentamicin (GE), while covering and protecting the wound was investigated. Chitosan (CHI) was associated with methoxy polyethylene glycol - polycaprolactone copolymer (mPEG-PCL) to prepare the blended wound dressing membranes. The use of copolymer mPEG-PCL was necessary to improve the compatibility between CHI and PCL. The association of CHI and PCL was required to control the water retention and release rate of encapsulated GE. In vitro release studies were performed with the mPEG-PCL/ CHI-GE membranes in order to evaluate the effect of copolymer concentration on the kinetics of GE release and water uptake. Reduced burst release rates and swelling ratios were observed for the 1/2 and 1/4 mPEG-PCL/CHI-GE membranes. In addition, all gentamicin-loaded membranes inhibited S. aureus and E. coli growth, and demonstrated color, moisture and thermal stability. Therefore, mPEG-PCL/CHI-GE membranes showed important features for potential wound dressing and drug delivery applications.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Univ Fed Alfenas, Inst Ciencia & Tecnol, Pocos De Caldas, MG, BrazilUniv Estadual Paulista, Inst Quim, Araraquara, SP, BrazilUniv Estadual Campinas, Fac Engn Quim, Campinas, SP, BrazilUniv Estadual Paulista, Inst Quim, Araraquara, SP, BrazilUniv Fed Sao Carlos, Dept Engenharia MaterialsUniv Fed AlfenasUniversidade Estadual Paulista (Unesp)Universidade Estadual de Campinas (UNICAMP)Silva Brianezi, Samira FaleirosCastro, Karine CappuccioPiazza, Rodolfo Debone [UNESP]Fernandes Melo, Maria do SocorroPereira, Rafael MatsumotoCosta Marques, Rodrigo Fernando [UNESP]Nogueira Campos, Maria Gabriela2018-11-26T16:04:56Z2018-11-26T16:04:56Z2018-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article10application/pdfhttp://dx.doi.org/10.1590/1980-5373-MR-2017-0951Materials Research-ibero-american Journal Of Materials. Sao Carlos: Univ Fed Sao Carlos, Dept Engenharia Materials, v. 21, n. 6, 10 p., 2018.1516-1439http://hdl.handle.net/11449/16055110.1590/1980-5373-MR-2017-0951S1516-14392018000600207WOS:000443384700001S1516-14392018000600207.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMaterials Research-ibero-american Journal Of Materials0,398info:eu-repo/semantics/openAccess2024-01-23T07:07:03Zoai:repositorio.unesp.br:11449/160551Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T23:45:34.543938Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Preparation and Characterization of Chitosan/mPEG-PCL Blended Membranes for Wound Dressing and Controlled Gentamicin Release |
title |
Preparation and Characterization of Chitosan/mPEG-PCL Blended Membranes for Wound Dressing and Controlled Gentamicin Release |
spellingShingle |
Preparation and Characterization of Chitosan/mPEG-PCL Blended Membranes for Wound Dressing and Controlled Gentamicin Release Silva Brianezi, Samira Faleiros Copolymer blend methoxy polyethylene glycol polycaprolactone antibiotic drug delivery |
title_short |
Preparation and Characterization of Chitosan/mPEG-PCL Blended Membranes for Wound Dressing and Controlled Gentamicin Release |
title_full |
Preparation and Characterization of Chitosan/mPEG-PCL Blended Membranes for Wound Dressing and Controlled Gentamicin Release |
title_fullStr |
Preparation and Characterization of Chitosan/mPEG-PCL Blended Membranes for Wound Dressing and Controlled Gentamicin Release |
title_full_unstemmed |
Preparation and Characterization of Chitosan/mPEG-PCL Blended Membranes for Wound Dressing and Controlled Gentamicin Release |
title_sort |
Preparation and Characterization of Chitosan/mPEG-PCL Blended Membranes for Wound Dressing and Controlled Gentamicin Release |
author |
Silva Brianezi, Samira Faleiros |
author_facet |
Silva Brianezi, Samira Faleiros Castro, Karine Cappuccio Piazza, Rodolfo Debone [UNESP] Fernandes Melo, Maria do Socorro Pereira, Rafael Matsumoto Costa Marques, Rodrigo Fernando [UNESP] Nogueira Campos, Maria Gabriela |
author_role |
author |
author2 |
Castro, Karine Cappuccio Piazza, Rodolfo Debone [UNESP] Fernandes Melo, Maria do Socorro Pereira, Rafael Matsumoto Costa Marques, Rodrigo Fernando [UNESP] Nogueira Campos, Maria Gabriela |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Univ Fed Alfenas Universidade Estadual Paulista (Unesp) Universidade Estadual de Campinas (UNICAMP) |
dc.contributor.author.fl_str_mv |
Silva Brianezi, Samira Faleiros Castro, Karine Cappuccio Piazza, Rodolfo Debone [UNESP] Fernandes Melo, Maria do Socorro Pereira, Rafael Matsumoto Costa Marques, Rodrigo Fernando [UNESP] Nogueira Campos, Maria Gabriela |
dc.subject.por.fl_str_mv |
Copolymer blend methoxy polyethylene glycol polycaprolactone antibiotic drug delivery |
topic |
Copolymer blend methoxy polyethylene glycol polycaprolactone antibiotic drug delivery |
description |
In this paper, a novel wound dressing membrane for controlled release of gentamicin (GE), while covering and protecting the wound was investigated. Chitosan (CHI) was associated with methoxy polyethylene glycol - polycaprolactone copolymer (mPEG-PCL) to prepare the blended wound dressing membranes. The use of copolymer mPEG-PCL was necessary to improve the compatibility between CHI and PCL. The association of CHI and PCL was required to control the water retention and release rate of encapsulated GE. In vitro release studies were performed with the mPEG-PCL/ CHI-GE membranes in order to evaluate the effect of copolymer concentration on the kinetics of GE release and water uptake. Reduced burst release rates and swelling ratios were observed for the 1/2 and 1/4 mPEG-PCL/CHI-GE membranes. In addition, all gentamicin-loaded membranes inhibited S. aureus and E. coli growth, and demonstrated color, moisture and thermal stability. Therefore, mPEG-PCL/CHI-GE membranes showed important features for potential wound dressing and drug delivery applications. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-11-26T16:04:56Z 2018-11-26T16:04:56Z 2018-01-01 |
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 |
http://dx.doi.org/10.1590/1980-5373-MR-2017-0951 Materials Research-ibero-american Journal Of Materials. Sao Carlos: Univ Fed Sao Carlos, Dept Engenharia Materials, v. 21, n. 6, 10 p., 2018. 1516-1439 http://hdl.handle.net/11449/160551 10.1590/1980-5373-MR-2017-0951 S1516-14392018000600207 WOS:000443384700001 S1516-14392018000600207.pdf |
url |
http://dx.doi.org/10.1590/1980-5373-MR-2017-0951 http://hdl.handle.net/11449/160551 |
identifier_str_mv |
Materials Research-ibero-american Journal Of Materials. Sao Carlos: Univ Fed Sao Carlos, Dept Engenharia Materials, v. 21, n. 6, 10 p., 2018. 1516-1439 10.1590/1980-5373-MR-2017-0951 S1516-14392018000600207 WOS:000443384700001 S1516-14392018000600207.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Materials Research-ibero-american Journal Of Materials 0,398 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
10 application/pdf |
dc.publisher.none.fl_str_mv |
Univ Fed Sao Carlos, Dept Engenharia Materials |
publisher.none.fl_str_mv |
Univ Fed Sao Carlos, Dept Engenharia Materials |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
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1808128240971153408 |