Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina

Detalhes bibliográficos
Ano de defesa: 2016
Autor(a) principal: Brianezi, Samira Faleiros Silva lattes
Orientador(a): Campos, Maria Gabriela Nogueira lattes
Banca de defesa: Hirano, Laos Alexandre, Melo, Maria Do Socorro Fernandes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Alfenas
Programa de Pós-Graduação: Programa de Pós-Graduação em Ciência e Engenharia de Materiais
Departamento: Instituto de Ciência e Tecnologia
País: Brasil
Palavras-chave em Português:
Área do conhecimento CNPq:
Link de acesso: https://repositorio.unifal-mg.edu.br/handle/123456789/1071
Resumo: It is currently of great interest to the manufacture of new materials for covering skin wounds. Chitosan (QUIT) is a functional material for its biodegradability characteristics, biocompatibility and non-toxicity. Furthermore, it can accelerate wound healing and hemostatic and bactericidal shown. Polycaprolactone (PCL) is a polyester with consistent properties and biodegradability, found in various biomedical applications such as controlled drug release. Methoxy polyethylene glycol copolymer (mPEG) and PCL, mPEG-PCL, is a biodegradable amphiphilic copolymer, making possible the interaction of PCL (hydrophobic) with QUIT which is hydrophilic. Gentamicin (GE) also hydrophilic, is one of the most widely used antibiotics due to its low cost and good stability. In this research were prepared QUIT membranes with mPEG-PCL and GE, which were characterized by scanning electron microscopy (SEM), colorimetry, look in the infrared (FTIR), thermogravimetry (TG), differential scanning calorimetry (DSC) humidity and percentage of swelling. Furthermore, GE release assays and in vitro antimicrobial activity were conducted using Escherichia coli and Staphylococcus aureus. The uniform distribution of the mPEG-PCL copolymer QUIT matrix and the presence of GE on their surface were observed in the SEM micrographs and tested by FTIR. Moreover, there was no significant change in color L membrane, which showed translucent, important property for wound coverings. DSC was obtained intermediate melting temperatures, comparing with the QUIT and mPEG-PCL, but higher than body temperature (37⁰C). The TG showed weight loss of membranes at temperatures above 37⁰C. The membranes were capable of absorbing buffer simulating the exuded fluids from the wound and had about 15% moisture. In the antimicrobial activity test, we observed inhibition halo around the charged membranes with GE, which had a lower initial release in the membrane with the highest concentration of mPEG-PCL in vitro release test.
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spelling Brianezi, Samira Faleiros Silvahttp://lattes.cnpq.br/1741478379427600Marques, Rodrigo Fernando Costahttp://lattes.cnpq.br/2115942621694174Hirano, Laos AlexandreMelo, Maria Do Socorro FernandesCampos, Maria Gabriela Nogueirahttp://lattes.cnpq.br/07367351765524702018-01-05T20:06:15Z2016-05-30BRIANEZI, Samira Faleiros Silva. Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina. 2016. 67 f. Dissertação (Mestrado em Ciência e Engenharia de Materiais) - Universidade Federal de Alfenas, Poços de Caldas, MG, 2016.https://repositorio.unifal-mg.edu.br/handle/123456789/1071It is currently of great interest to the manufacture of new materials for covering skin wounds. Chitosan (QUIT) is a functional material for its biodegradability characteristics, biocompatibility and non-toxicity. Furthermore, it can accelerate wound healing and hemostatic and bactericidal shown. Polycaprolactone (PCL) is a polyester with consistent properties and biodegradability, found in various biomedical applications such as controlled drug release. Methoxy polyethylene glycol copolymer (mPEG) and PCL, mPEG-PCL, is a biodegradable amphiphilic copolymer, making possible the interaction of PCL (hydrophobic) with QUIT which is hydrophilic. Gentamicin (GE) also hydrophilic, is one of the most widely used antibiotics due to its low cost and good stability. In this research were prepared QUIT membranes with mPEG-PCL and GE, which were characterized by scanning electron microscopy (SEM), colorimetry, look in the infrared (FTIR), thermogravimetry (TG), differential scanning calorimetry (DSC) humidity and percentage of swelling. Furthermore, GE release assays and in vitro antimicrobial activity were conducted using Escherichia coli and Staphylococcus aureus. The uniform distribution of the mPEG-PCL copolymer QUIT matrix and the presence of GE on their surface were observed in the SEM micrographs and tested by FTIR. Moreover, there was no significant change in color L membrane, which showed translucent, important property for wound coverings. DSC was obtained intermediate melting temperatures, comparing with the QUIT and mPEG-PCL, but higher than body temperature (37⁰C). The TG showed weight loss of membranes at temperatures above 37⁰C. The membranes were capable of absorbing buffer simulating the exuded fluids from the wound and had about 15% moisture. In the antimicrobial activity test, we observed inhibition halo around the charged membranes with GE, which had a lower initial release in the membrane with the highest concentration of mPEG-PCL in vitro release test.Atualmente é de grande interesse a fabricação de novos materiais para o recobrimento de feridas de pele. A quitosana (QUIT) é um material funcional por suas características de biodegradabilidade, biocompatibilidade e não toxicidade. Além disso, pode acelerar a cicatrização de feridas e se mostra hemostática e bactericida. A policaprolactona (PCL) é um poliéster com propriedades compatíveis e biodegradabilidade, encontrado em várias aplicações biomédicas, como liberação controlada de fármacos. O copolímero de metoxi polietileno glicol (mPEG) e PCL, o mPEG-PCL, é um copolímero anfifílico biodegradável, tornando possível a interação da PCL (hidrofóbica) com a QUI, que é hidrofílica. A gentamicina (GE), também hidrofílica, é um dos antibióticos mais utilizados devido ao seu baixo custo e boa estabilidade. Nesta pesquisa foram preparadas membranas de QUIT com mPEG-PCL e GE, as quais foram caracterizadas por microscopia eletrônica de varredura (MEV), colorimetria, analise na região do infravermelho (FTIR), termogravimetria (TG), calorimetria diferencial exploratória (DSC), umidade e porcentagem de intumescimento. Ainda, foram realizados ensaios de liberação de GE in vitro e da atividade antimicrobiana, utilizando Escherichia coli e Staphylococcus aureus. A distribuição uniforme do copolímero mPEG-PCL na matriz de QUIT e a presença de GE na superfície das mesmas foram observadas nas micrografias de MEV e comprovadas por FTIR. Além disso, não houve alteração significativa na cor L das membranas, que se mostraram translucidas, propriedade importante para recobrimentos de ferida. Por DSC, obteve-se temperaturas de fusão intermediarias, comparando-se com as da QUIT e do mPEG-PCL, porém superiores à temperatura corpórea (37⁰C). A TG mostrou perda de massa das membranas em temperaturas superiores a 37⁰C. As membranas foram capazes de absorver tampão, simulando os fluidos exsudados da ferida e apresentaram cerca de 15% de umidade. Nos testes de atividade antimicrobiana, foi possível observar halo de inibição ao redor das membranas carregadas com GE, que teve uma liberação inicial menor na membrana com maior concentração de mPEG-PCL no ensaio de liberação in vitro.application/pdfporUniversidade Federal de AlfenasPrograma de Pós-Graduação em Ciência e Engenharia de MateriaisUNIFAL-MGBrasilInstituto de Ciência e Tecnologiainfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/4.0/Gentamicina.Copolímeros.Quitosana.Cicatrização de feridas.MATERIAIS NAO METALICOS::POLIMEROS, APLICACOESPreparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicinaPreparation and characterization of chitosan membranes and mPEG- PCL for covering wounds and controlled release of gentamicininfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/publishedVersion-42974172594986389316006003372037382386094482reponame:Repositório Institucional da Universidade Federal de Alfenas - RiUnifalinstname:Universidade Federal de Alfenas (UNIFAL)instacron:UNIFALBrianezi, Samira Faleiros SilvaLICENSElicense.txtlicense.txttext/plain; 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dc.title.pt-BR.fl_str_mv Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina
dc.title.alternative.eng.fl_str_mv Preparation and characterization of chitosan membranes and mPEG- PCL for covering wounds and controlled release of gentamicin
title Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina
spellingShingle Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina
Brianezi, Samira Faleiros Silva
Gentamicina.
Copolímeros.
Quitosana.
Cicatrização de feridas.
MATERIAIS NAO METALICOS::POLIMEROS, APLICACOES
title_short Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina
title_full Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina
title_fullStr Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina
title_full_unstemmed Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina
title_sort Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina
author Brianezi, Samira Faleiros Silva
author_facet Brianezi, Samira Faleiros Silva
author_role author
dc.contributor.author.fl_str_mv Brianezi, Samira Faleiros Silva
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/1741478379427600
dc.contributor.advisor-co1.fl_str_mv Marques, Rodrigo Fernando Costa
dc.contributor.advisor-co1Lattes.fl_str_mv http://lattes.cnpq.br/2115942621694174
dc.contributor.referee1.fl_str_mv Hirano, Laos Alexandre
dc.contributor.referee2.fl_str_mv Melo, Maria Do Socorro Fernandes
dc.contributor.advisor1.fl_str_mv Campos, Maria Gabriela Nogueira
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/0736735176552470
contributor_str_mv Marques, Rodrigo Fernando Costa
Hirano, Laos Alexandre
Melo, Maria Do Socorro Fernandes
Campos, Maria Gabriela Nogueira
dc.subject.por.fl_str_mv Gentamicina.
Copolímeros.
Quitosana.
Cicatrização de feridas.
topic Gentamicina.
Copolímeros.
Quitosana.
Cicatrização de feridas.
MATERIAIS NAO METALICOS::POLIMEROS, APLICACOES
dc.subject.cnpq.fl_str_mv MATERIAIS NAO METALICOS::POLIMEROS, APLICACOES
description It is currently of great interest to the manufacture of new materials for covering skin wounds. Chitosan (QUIT) is a functional material for its biodegradability characteristics, biocompatibility and non-toxicity. Furthermore, it can accelerate wound healing and hemostatic and bactericidal shown. Polycaprolactone (PCL) is a polyester with consistent properties and biodegradability, found in various biomedical applications such as controlled drug release. Methoxy polyethylene glycol copolymer (mPEG) and PCL, mPEG-PCL, is a biodegradable amphiphilic copolymer, making possible the interaction of PCL (hydrophobic) with QUIT which is hydrophilic. Gentamicin (GE) also hydrophilic, is one of the most widely used antibiotics due to its low cost and good stability. In this research were prepared QUIT membranes with mPEG-PCL and GE, which were characterized by scanning electron microscopy (SEM), colorimetry, look in the infrared (FTIR), thermogravimetry (TG), differential scanning calorimetry (DSC) humidity and percentage of swelling. Furthermore, GE release assays and in vitro antimicrobial activity were conducted using Escherichia coli and Staphylococcus aureus. The uniform distribution of the mPEG-PCL copolymer QUIT matrix and the presence of GE on their surface were observed in the SEM micrographs and tested by FTIR. Moreover, there was no significant change in color L membrane, which showed translucent, important property for wound coverings. DSC was obtained intermediate melting temperatures, comparing with the QUIT and mPEG-PCL, but higher than body temperature (37⁰C). The TG showed weight loss of membranes at temperatures above 37⁰C. The membranes were capable of absorbing buffer simulating the exuded fluids from the wound and had about 15% moisture. In the antimicrobial activity test, we observed inhibition halo around the charged membranes with GE, which had a lower initial release in the membrane with the highest concentration of mPEG-PCL in vitro release test.
publishDate 2016
dc.date.issued.fl_str_mv 2016-05-30
dc.date.accessioned.fl_str_mv 2018-01-05T20:06:15Z
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dc.identifier.citation.fl_str_mv BRIANEZI, Samira Faleiros Silva. Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina. 2016. 67 f. Dissertação (Mestrado em Ciência e Engenharia de Materiais) - Universidade Federal de Alfenas, Poços de Caldas, MG, 2016.
dc.identifier.uri.fl_str_mv https://repositorio.unifal-mg.edu.br/handle/123456789/1071
identifier_str_mv BRIANEZI, Samira Faleiros Silva. Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina. 2016. 67 f. Dissertação (Mestrado em Ciência e Engenharia de Materiais) - Universidade Federal de Alfenas, Poços de Caldas, MG, 2016.
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dc.publisher.country.fl_str_mv Brasil
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