Preparação e caracterização de membranas de quitosana e mPEG-PCL para recobrimento de feridas e liberação controlada de gentamicina
| Ano de defesa: | 2016 |
|---|---|
| Autor(a) principal: | |
| Orientador(a): | |
| Banca de defesa: | , |
| 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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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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info:eu-repo/semantics/masterThesis |
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info:eu-repo/semantics/publishedVersion |
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masterThesis |
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publishedVersion |
| 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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https://repositorio.unifal-mg.edu.br/handle/123456789/1071 |
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por |
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por |
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600 600 |
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info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-nd/4.0/ |
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http://creativecommons.org/licenses/by-nc-nd/4.0/ |
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Universidade Federal de Alfenas |
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Programa de Pós-Graduação em Ciência e Engenharia de Materiais |
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UNIFAL-MG |
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Brasil |
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Instituto de Ciência e Tecnologia |
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Universidade Federal de Alfenas |
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31555718c4fc75849dd08f27935d4f6b 4afdbb8c545fd630ea7db775da747b2f d41d8cd98f00b204e9800998ecf8427e d41d8cd98f00b204e9800998ecf8427e e5910c072c8ab48dcc5f98c767dd74e6 e68026e08b88f03e16cfa25f7acfd5d6 836779fe5dde20f30fabdb6b2892e63d |
| bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 MD5 MD5 MD5 |
| repository.name.fl_str_mv |
Repositório Institucional da Universidade Federal de Alfenas - RiUnifal - Universidade Federal de Alfenas (UNIFAL) |
| repository.mail.fl_str_mv |
repositorio@unifal-mg.edu.br |
| _version_ |
1859830895746220032 |