Preparation and Characterization of Chitosan/mPEG-PCL Blended Membranes for Wound Dressing and Controlled Gentamicin Release

Detalhes bibliográficos
Autor(a) principal: Silva Brianezi, Samira Faleiros
Data de Publicação: 2018
Outros Autores: Castro, Karine Cappuccio, Piazza, Rodolfo Debone [UNESP], Fernandes Melo, Maria do Socorro, Pereira, Rafael Matsumoto, Costa Marques, Rodrigo Fernando [UNESP], Nogueira Campos, Maria Gabriela
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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spelling 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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