Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos

Detalhes bibliográficos
Ano de defesa: 2022
Autor(a) principal: Ferreira, João Otávio
Orientador(a): Francisco, Kelly Roberta lattes
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de São Carlos
Câmpus Sorocaba
Programa de Pós-Graduação: Programa de Pós-Graduação em Ciência dos Materiais - PPGCM-So
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: https://repositorio.ufscar.br/handle/20.500.14289/16749
Resumo: This master’s thesis aimed to develop electrospun microfibers formed by hydroxypropylcellulose acetate succinate (HPMC-AS), zein and celulose nanofibril to be used in the release of metronidazole (MDZ) and metronidazole benzoate (BMDZ), which are important drugs in the treatment of periodontal disease. The morphology, chemical composition and cristalinity of the membranes were analyzed by scanning electron microscopy (SEM), infrared (FTIR) and X-ray diffraction (XRD), respectively. The termal behavior of the fibers was investigated by differential scanning calorimetry (DSC) and thermogravimetry (TGA). Furthermore, the drug release profile and the kinetic mechanism were also evaluated. The results showed that microfibers were produced without defects, amorphous and with average diameters of 1,689; 1,298 and 1,395μm mμ for membranes formed by HPMC-AS/zein in the proportion of 40/60, 50/50 and 60/40 (% w/w), respectively. Microfibers formed by HPMC-AS/zein 60/40 presented the smallest average diameter and fewer defects on their surface, which is the reason this system was chosen for drug delivery purposes. However, after addition of the drugs, extensive crystallization of the drugs was visualized on the fiber surface and also many deffects were produced. Thus, celulose nanofibrils were added to this system, producing defect-free and semi-crystalline fibers with an average diameter of 1,968; 1,076 and 1,510μm for systems containing 20% MDZ / 20% BMDZ, 40% MDZ and 40% BMDZ, respectively. FTIR, XRD and DSC results suggested intermolecular interactions via hydrogen bonding among polymeric chains and the drugs, with a decrease in the melting temperature of the drug crystals present in the fibers. Drug release profile from fibers containing 40% of each drug showed a fast release of MDZ molecules in the first 6h (80%), while BMDZ showed a slower release (30%). For the membrane containing 20% of each drug, the drug release decreased with maintenance of 55% for at least 5 days, concomitantly with suficiente therapeutic amounts of the drugs in the first hours (40%). In other words, electrospun fibers of HPMC-AS, zein and cellulose nanofibril containing metronidazole and metronidazole benzoate are strategic materials that provides na immediate release of the drugs for the initial treatment of periodontitis and a slow release for the maintenance of drugs in the oral tract for hours/days.
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spelling Ferreira, João OtávioFrancisco, Kelly Robertahttp://lattes.cnpq.br/0422652925722673Duarte, Maíra Peres Ferreirahttp://lattes.cnpq.br/5201758415555524https://lattes.cnpq.br/42066152509758260e3f555d-a954-4c23-9995-2873c1f22ab52022-09-30T12:39:55Z2022-09-30T12:39:55Z2022-09-09FERREIRA, João Otávio. Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos. 2022. Dissertação (Mestrado em Ciência dos Materiais) – Universidade Federal de São Carlos, Sorocaba, 2022. Disponível em: https://repositorio.ufscar.br/handle/20.500.14289/16749.https://repositorio.ufscar.br/handle/20.500.14289/16749This master’s thesis aimed to develop electrospun microfibers formed by hydroxypropylcellulose acetate succinate (HPMC-AS), zein and celulose nanofibril to be used in the release of metronidazole (MDZ) and metronidazole benzoate (BMDZ), which are important drugs in the treatment of periodontal disease. The morphology, chemical composition and cristalinity of the membranes were analyzed by scanning electron microscopy (SEM), infrared (FTIR) and X-ray diffraction (XRD), respectively. The termal behavior of the fibers was investigated by differential scanning calorimetry (DSC) and thermogravimetry (TGA). Furthermore, the drug release profile and the kinetic mechanism were also evaluated. The results showed that microfibers were produced without defects, amorphous and with average diameters of 1,689; 1,298 and 1,395μm mμ for membranes formed by HPMC-AS/zein in the proportion of 40/60, 50/50 and 60/40 (% w/w), respectively. Microfibers formed by HPMC-AS/zein 60/40 presented the smallest average diameter and fewer defects on their surface, which is the reason this system was chosen for drug delivery purposes. However, after addition of the drugs, extensive crystallization of the drugs was visualized on the fiber surface and also many deffects were produced. Thus, celulose nanofibrils were added to this system, producing defect-free and semi-crystalline fibers with an average diameter of 1,968; 1,076 and 1,510μm for systems containing 20% MDZ / 20% BMDZ, 40% MDZ and 40% BMDZ, respectively. FTIR, XRD and DSC results suggested intermolecular interactions via hydrogen bonding among polymeric chains and the drugs, with a decrease in the melting temperature of the drug crystals present in the fibers. Drug release profile from fibers containing 40% of each drug showed a fast release of MDZ molecules in the first 6h (80%), while BMDZ showed a slower release (30%). For the membrane containing 20% of each drug, the drug release decreased with maintenance of 55% for at least 5 days, concomitantly with suficiente therapeutic amounts of the drugs in the first hours (40%). In other words, electrospun fibers of HPMC-AS, zein and cellulose nanofibril containing metronidazole and metronidazole benzoate are strategic materials that provides na immediate release of the drugs for the initial treatment of periodontitis and a slow release for the maintenance of drugs in the oral tract for hours/days.A presente dissertação de mestrado objetivou o desenvolvimento de microfibras eletrofiadas formadas por hidroxipropilcelulose acetato succinato (HPMC-AS), zeína e nanofibrila de celulose para serem utilizadas na liberação dos fármacos metronidazol (MDZ) e benzoato de metronidazol (BMDZ), os quais auxiliam no tratamento de doença periodontal. A morfologia, a composição química e a cristalinidade das membranas foram analisadas por microscopia eletrônica de varredura (MEV), infravermelho (FTIR) e difração de Raios-X (DRX), respectivamente. O comportamento térmico das fibras foi investigado por calorimetria exploratória diferencial (DSC) e termogravimetria (TGA). Ademais, o perfil de liberação das drogas a partir das fibras poliméricas e a cinética de liberação dos fármacos também foram avaliados. Os resultados mostraram que microfibras sem defeitos, amorfas e com diâmetros de 1,689; 1,298; 1,395μm foram produzidas a partir das proporções HPMC-AS/zeína de 40/60, 50/50 e 60/40 (% m/m), respectivamente. As microfibras obtidas a partir da proporção HPMC-AS/zeína 60/40 (% m/m) apresentaram o menor diâmetro médio e menos defeitos superficiais, sendo essa a proporção escolhida para a construção dos sistemas de liberação. Entretanto, após a adição dos fármacos verificou-se uma ampla cristalização dos mesmos na superfície do material e a formação de fibras com muitos defeitos. Assim, nanofibrilas de celulose foram adicionadas a esse sistema, produzindo fibras sem defeitos, semi-cristalinas com diâmetro médio de 1,968; 1,076; 1,510μm para os sistemas contendo 20% MDZ/20% BMDZ, 40% MDZ e 40% BMDZ, respectivamente. Os resultados de FTIR, DRX e DSC sugerem o estabelecimento de interações intermoleculares via ligação de hidrogênio entre as cadeias poliméricas e os fármacos, com diminuição da temperatura de fusão dos cristais dos fármacos presentes nas fibras. Os ensaios de liberação dos fármacos a partir das fibras contendo 40% de cada droga mostraram uma rápida liberação do MDZ nas primeiras 6h (80%), enquanto o BMDZ mostrou uma liberação mais lenta (30%). Para a membrana contendo 20% de cada droga, verificou-se uma diminuição na liberação dos fármacos com a manutenção de 55% de liberação por pelo menos 5 dias, concomitantemente com quantidades terapêuticas suficientes nas primeiras horas de liberação (40%). Ou seja, as fibras eletrofiadas de HPMC-AS, zeina e nanofibrila de celulose contendo os fármacos metronidazol e benzoato de metronidazol apresentam-se como um sistema que dispõe uma liberação imediata das drogas para o tratamento inicial da periodontite e uma liberação lenta para a manutenção dos fármacos no trato oral por horas/dias.Não recebi financiamentoporUniversidade Federal de São CarlosCâmpus SorocabaPrograma de Pós-Graduação em Ciência dos Materiais - PPGCM-SoUFSCarAttribution-NonCommercial-NoDerivs 3.0 Brazilhttp://creativecommons.org/licenses/by-nc-nd/3.0/br/info:eu-repo/semantics/openAccessEletrofiaçãoMicrofibrasHidroxipropilcelulose acetato succinatoZeínaNanofibrila de celuloseMetronidazol e benzoato de metronidazolElectrospinningMicrofibersHydroxypropyl Cellulose Acetate SuccinateZeinCellulose nanofibrilMetronidazole and Metronidazole BenzoateCIENCIAS EXATAS E DA TERRA::QUIMICASíntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacosSynthesis of zein/hydroxypropylmethylcellulose and nanofibril biopolymer microfibers for controlled drug deliveryinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis60060006ddea16-af5f-4bdb-bfd4-0022cd5176e2reponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8811https://repositorio.ufscar.br/bitstreams/5240de6a-2b24-48d9-b037-f3965e5bb69b/downloade39d27027a6cc9cb039ad269a5db8e34MD53falseAnonymousREADORIGINALDissertação - João Otávio Ferreira - Versão final.pdfDissertação - João Otávio Ferreira - Versão final.pdfDissertação de mestradoapplication/pdf2278616https://repositorio.ufscar.br/bitstreams/fd374078-699c-430d-83a5-b00ea45d4bdd/downloadbf721cae03fe2eb52572fa81a177cbb4MD51trueAnonymousREADCarta comprovante.pdfCarta comprovante.pdfCarta comprovanteapplication/pdf184875https://repositorio.ufscar.br/bitstreams/442523ff-8043-47fa-9336-6b1cb80905a5/download1b9e1adc6932bc0d256147e786334feeMD52falseTEXTDissertação - João Otávio Ferreira - Versão final.pdf.txtDissertação - João Otávio Ferreira - Versão final.pdf.txtExtracted texttext/plain154184https://repositorio.ufscar.br/bitstreams/9a82b079-68e6-4411-91f1-781c728aade8/download08edf8c284e31192cf018bcf6641b90cMD54falseAnonymousREADCarta comprovante.pdf.txtCarta comprovante.pdf.txtExtracted texttext/plain1486https://repositorio.ufscar.br/bitstreams/57ae3ff7-115b-4ef1-a99b-a19c6b9aba28/downloadd3022c6edebe4c131fa6d0d44f443c1cMD56falseTHUMBNAILDissertação - João Otávio Ferreira - Versão final.pdf.jpgDissertação - João Otávio Ferreira - Versão final.pdf.jpgIM Thumbnailimage/jpeg6553https://repositorio.ufscar.br/bitstreams/4351c940-7cd0-4033-bb11-9dfb563e5985/downloadbaf8e466a43a7c66c839fb880d82b35eMD55falseAnonymousREADCarta comprovante.pdf.jpgCarta comprovante.pdf.jpgIM Thumbnailimage/jpeg6994https://repositorio.ufscar.br/bitstreams/f560dcc3-5f8e-4468-9154-e646ca36ce44/downloadd18acb98004de8147f8ca72491c9dea6MD57false20.500.14289/167492025-02-05 22:08:40.813http://creativecommons.org/licenses/by-nc-nd/3.0/br/Attribution-NonCommercial-NoDerivs 3.0 Brazilopen.accessoai:repositorio.ufscar.br:20.500.14289/16749https://repositorio.ufscar.brRepositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestrepositorio.sibi@ufscar.bropendoar:43222025-02-06T01:08:40Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)false
dc.title.por.fl_str_mv Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos
dc.title.alternative.eng.fl_str_mv Synthesis of zein/hydroxypropylmethylcellulose and nanofibril biopolymer microfibers for controlled drug delivery
title Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos
spellingShingle Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos
Ferreira, João Otávio
Eletrofiação
Microfibras
Hidroxipropilcelulose acetato succinato
Zeína
Nanofibrila de celulose
Metronidazol e benzoato de metronidazol
Electrospinning
Microfibers
Hydroxypropyl Cellulose Acetate Succinate
Zein
Cellulose nanofibril
Metronidazole and Metronidazole Benzoate
CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos
title_full Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos
title_fullStr Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos
title_full_unstemmed Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos
title_sort Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos
author Ferreira, João Otávio
author_facet Ferreira, João Otávio
author_role author
dc.contributor.authorlattes.por.fl_str_mv https://lattes.cnpq.br/4206615250975826
dc.contributor.author.fl_str_mv Ferreira, João Otávio
dc.contributor.advisor1.fl_str_mv Francisco, Kelly Roberta
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/0422652925722673
dc.contributor.advisor-co1.fl_str_mv Duarte, Maíra Peres Ferreira
dc.contributor.advisor-co1Lattes.fl_str_mv http://lattes.cnpq.br/5201758415555524
dc.contributor.authorID.fl_str_mv 0e3f555d-a954-4c23-9995-2873c1f22ab5
contributor_str_mv Francisco, Kelly Roberta
Duarte, Maíra Peres Ferreira
dc.subject.por.fl_str_mv Eletrofiação
Microfibras
Hidroxipropilcelulose acetato succinato
Zeína
Nanofibrila de celulose
Metronidazol e benzoato de metronidazol
topic Eletrofiação
Microfibras
Hidroxipropilcelulose acetato succinato
Zeína
Nanofibrila de celulose
Metronidazol e benzoato de metronidazol
Electrospinning
Microfibers
Hydroxypropyl Cellulose Acetate Succinate
Zein
Cellulose nanofibril
Metronidazole and Metronidazole Benzoate
CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.eng.fl_str_mv Electrospinning
Microfibers
Hydroxypropyl Cellulose Acetate Succinate
Zein
Cellulose nanofibril
Metronidazole and Metronidazole Benzoate
dc.subject.cnpq.fl_str_mv CIENCIAS EXATAS E DA TERRA::QUIMICA
description This master’s thesis aimed to develop electrospun microfibers formed by hydroxypropylcellulose acetate succinate (HPMC-AS), zein and celulose nanofibril to be used in the release of metronidazole (MDZ) and metronidazole benzoate (BMDZ), which are important drugs in the treatment of periodontal disease. The morphology, chemical composition and cristalinity of the membranes were analyzed by scanning electron microscopy (SEM), infrared (FTIR) and X-ray diffraction (XRD), respectively. The termal behavior of the fibers was investigated by differential scanning calorimetry (DSC) and thermogravimetry (TGA). Furthermore, the drug release profile and the kinetic mechanism were also evaluated. The results showed that microfibers were produced without defects, amorphous and with average diameters of 1,689; 1,298 and 1,395μm mμ for membranes formed by HPMC-AS/zein in the proportion of 40/60, 50/50 and 60/40 (% w/w), respectively. Microfibers formed by HPMC-AS/zein 60/40 presented the smallest average diameter and fewer defects on their surface, which is the reason this system was chosen for drug delivery purposes. However, after addition of the drugs, extensive crystallization of the drugs was visualized on the fiber surface and also many deffects were produced. Thus, celulose nanofibrils were added to this system, producing defect-free and semi-crystalline fibers with an average diameter of 1,968; 1,076 and 1,510μm for systems containing 20% MDZ / 20% BMDZ, 40% MDZ and 40% BMDZ, respectively. FTIR, XRD and DSC results suggested intermolecular interactions via hydrogen bonding among polymeric chains and the drugs, with a decrease in the melting temperature of the drug crystals present in the fibers. Drug release profile from fibers containing 40% of each drug showed a fast release of MDZ molecules in the first 6h (80%), while BMDZ showed a slower release (30%). For the membrane containing 20% of each drug, the drug release decreased with maintenance of 55% for at least 5 days, concomitantly with suficiente therapeutic amounts of the drugs in the first hours (40%). In other words, electrospun fibers of HPMC-AS, zein and cellulose nanofibril containing metronidazole and metronidazole benzoate are strategic materials that provides na immediate release of the drugs for the initial treatment of periodontitis and a slow release for the maintenance of drugs in the oral tract for hours/days.
publishDate 2022
dc.date.accessioned.fl_str_mv 2022-09-30T12:39:55Z
dc.date.available.fl_str_mv 2022-09-30T12:39:55Z
dc.date.issued.fl_str_mv 2022-09-09
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dc.identifier.citation.fl_str_mv FERREIRA, João Otávio. Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos. 2022. Dissertação (Mestrado em Ciência dos Materiais) – Universidade Federal de São Carlos, Sorocaba, 2022. Disponível em: https://repositorio.ufscar.br/handle/20.500.14289/16749.
dc.identifier.uri.fl_str_mv https://repositorio.ufscar.br/handle/20.500.14289/16749
identifier_str_mv FERREIRA, João Otávio. Síntese de microfibras biopoliméricas de zeína/hidroxipropilmetilcelulose e nanofibrila para liberação controlada de fármacos. 2022. Dissertação (Mestrado em Ciência dos Materiais) – Universidade Federal de São Carlos, Sorocaba, 2022. Disponível em: https://repositorio.ufscar.br/handle/20.500.14289/16749.
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dc.publisher.none.fl_str_mv Universidade Federal de São Carlos
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