Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA)

Detalhes bibliográficos
Ano de defesa: 2017
Autor(a) principal: Reis, Malu Maria Lucas dos lattes
Orientador(a): Damasceno, Bolívar Ponciano Goulart de Lima lattes
Banca de defesa: Machado, Giovanna lattes, Lima, Rosemary Sousa Cunha lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Estadual da Paraíba
Programa de Pós-Graduação: Programa de Pós-Graduação em Ciências Farmacêuticas - PPGCF
Departamento: Pró-Reitoria de Pós-Graduação e Pesquisa - PRPGP
País: BR
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: https://repositorio.uepb.edu.br/handle/123456789/73287
Resumo: Infectious diseases are responsible for about 25% deaths worldwide and 45% in underdeveloped countries. Antimicrobials are usually used to fight an established infection, they aim either to eliminate or to impede bacterial growth without causing harm to the patient. Flavone, a molecule derived from flavonoids, has evidence of bactericidal activity, with LogP of 3.37 which indicates high lipophilicity. Therefore, it needs a carrier system with lipophilic characteristics, such as microemulsions (ME) and nanoemulsions (NE) O/A, that are systems indicated to its incorporation and use as a novel drug delivery system (NDDS). The aim of this work was to develop nano/microemulsion systems for the incorporation of flavone, aiming topical application, characterizing them physico-chemically, defining a methodology for drug dosing. For the development of the systems and for the choice of formulations to be studied, the construction of the pseudo-ternary phase diagram was performed, followed by incorporation of the drug (1 mg/mL). From this, the physicochemical characterization of the samples was initiated: macroscopic evaluation, isotropy, pH measurement, refractive index, differential scanning calorimetry (DSC), transmission electron microscopy (MET), Zeta potential, droplet size and polydispersity index. In addition, the validation of an analytical method for flavone assay by UV-VIS spectrophotometer and high-performance liquid chromatography (HPLC) was performed. The NE developed was composed of 10.8% oil phase (isopropyl myristate), 25.87% surfactants (polyethylene glycol (15)-hydroxystearate/sorbitan monooleate 80) and 63.33% water. The ME has 34.5% oil phase, 34.5% surfactants and 31% water. Through isotropy, DSC and MET it was possible to prove that the nanoemulsion is O/A and the ME is a bicontinuous system. The analytical methods were validated, both linear, selective, accurate and robust. The present study was relevant for the area of pharmaceutical technology. We sought to develop novel systems with relevant therapeutic potential, since the proposed systems are unprecedented and the drug has the potential to treat antimicrobial diseases.
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spelling 2018-05-23T16:59:44Z2026-02-27T10:27:46Z2017-02-16REIS, M. M. L. dos. Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA). 2017. 69f. Dissertação (Programa de Pós-Graduação em Ciências Farmacêuticas - PPGCF) - Universidade Estadual da Paraíba, Campina Grande, 2017.https://repositorio.uepb.edu.br/handle/123456789/7328724004014014P8Infectious diseases are responsible for about 25% deaths worldwide and 45% in underdeveloped countries. Antimicrobials are usually used to fight an established infection, they aim either to eliminate or to impede bacterial growth without causing harm to the patient. Flavone, a molecule derived from flavonoids, has evidence of bactericidal activity, with LogP of 3.37 which indicates high lipophilicity. Therefore, it needs a carrier system with lipophilic characteristics, such as microemulsions (ME) and nanoemulsions (NE) O/A, that are systems indicated to its incorporation and use as a novel drug delivery system (NDDS). The aim of this work was to develop nano/microemulsion systems for the incorporation of flavone, aiming topical application, characterizing them physico-chemically, defining a methodology for drug dosing. For the development of the systems and for the choice of formulations to be studied, the construction of the pseudo-ternary phase diagram was performed, followed by incorporation of the drug (1 mg/mL). From this, the physicochemical characterization of the samples was initiated: macroscopic evaluation, isotropy, pH measurement, refractive index, differential scanning calorimetry (DSC), transmission electron microscopy (MET), Zeta potential, droplet size and polydispersity index. In addition, the validation of an analytical method for flavone assay by UV-VIS spectrophotometer and high-performance liquid chromatography (HPLC) was performed. The NE developed was composed of 10.8% oil phase (isopropyl myristate), 25.87% surfactants (polyethylene glycol (15)-hydroxystearate/sorbitan monooleate 80) and 63.33% water. The ME has 34.5% oil phase, 34.5% surfactants and 31% water. Through isotropy, DSC and MET it was possible to prove that the nanoemulsion is O/A and the ME is a bicontinuous system. The analytical methods were validated, both linear, selective, accurate and robust. The present study was relevant for the area of pharmaceutical technology. We sought to develop novel systems with relevant therapeutic potential, since the proposed systems are unprecedented and the drug has the potential to treat antimicrobial diseases.As doenças infecto-contagiosas são responsáveis por cerca de 25% das mortes em todo o mundo e 45% nos países subdesenvolvidos. Os antimicrobianos são utilizados para combater uma infecção estabelecida, possuindo a finalidade de eliminar ou impedir o crescimento bacteriano, sem causar danos ao paciente. Os flavonoides surgem como mais uma alternativa no tratamento antibacteriano. A flavona, molécula derivada dos flavonoides, possui indícios de sua atividade bactericida, com LogP de 3,37, que indica alta lipofilia. Logo, necessitamos de um sistema carreador com características lipofílicas, sendo carreadores lipídicos, como as microemulsões (ME) e nanoemulsões (NE) do tipo O/A, sistemas indicados para a sua incorporação e utilização como um novo sistema de liberação de fármacos (NSLF). Os objetivos deste trabalho foram desenvolver sistemas nano/microemulsionados para incorporação da flavona, almejando a aplicação tópica, caracterizá-los físico-quimicamente, definir uma metodologia para doseamento do fármaco. Para o desenvolvimento dos sistemas e escolha das formulações a serem estudadas foi realizada a construção do diagrama de fases pseudo-ternário, seguido de incorporação do fármaco (1 mg/mL). A partir disso, iniciaram-se as devidas caracterizações físico-químicas das amostras: avaliação macroscópica, isotropia, medição do pH, índice de refração, calorimetria exploratória diferencial (DSC), microscopia eletrônica de transmissão (MET), potencial Zeta, tamanho de gotícula e índice de polidispersão, além da validação de método analítico para doseamento de flavona por espectrofotômetro UV-VIS e por cromatrografia líquida de alta eficiência (CLAE). A NE desenvolvida foi constituída de 10,8% de fase oleosa (miristato de isopropila), 25,87% de tensoativos (polietilenoglicol (15)-hidroxiestearato/monooleato de Sorbitan 80) e 63,33% de água. Já a microemulsão, possui 34,5% de fase oleosa, 34,5% de tensoativos e 31% de água. Através da isotropia, DSC e MET foi possível provar que a nanoemulsão é O/A e a microemulsão é bicontínua. Os métodos analíticos foram validados, sendo ambos linear, seletivos, precisos, exatos e robustos. O presente estudo mostrou-se relevante para área de tecnologia farmacêutica. Buscou-se desenvolver sistemas inéditos com potencialidade terapêutica relevante, pois os sistemas propostos são inéditos e o fármaco apresenta potencialidade para tratamento de doenças antimicrobianas.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfUniversidade Estadual da ParaíbaPrograma de Pós-Graduação em Ciências Farmacêuticas - PPGCFUEPBBRPró-Reitoria de Pós-Graduação e Pesquisa - PRPGPFlavoneNanoemulsionMicroemulsionCIENCIAS DA SAUDEMicroemulsãoFlavonaNanoemulsãoSistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA)info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisMachado, Giovannahttp://lattes.cnpq.br/2869680994075940Lima, Rosemary Sousa Cunhahttp://lattes.cnpq.br/9097934027901875Damasceno, Bolívar Ponciano Goulart de Limahttp://lattes.cnpq.br/6407334157973308http://lattes.cnpq.br/7441078028137833Reis, Malu Maria Lucas dosinfo:eu-repo/semantics/openAccessporreponame:Repositório Institucional da Universidade Estadual da Paraíba (UEPB)instname:Universidade Estadual da Paraíba (UEPB)instacron:UEPBLICENSElicense.txtlicense.txttext/plain; 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dc.title.none.fl_str_mv Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA)
title Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA)
spellingShingle Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA)
Reis, Malu Maria Lucas dos
Flavone
Nanoemulsion
Microemulsion
CIENCIAS DA SAUDE
Microemulsão
Flavona
Nanoemulsão
title_short Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA)
title_full Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA)
title_fullStr Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA)
title_full_unstemmed Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA)
title_sort Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA)
author Reis, Malu Maria Lucas dos
author_facet Reis, Malu Maria Lucas dos
author_role author
dc.contributor.referee1.fl_str_mv Machado, Giovanna
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/2869680994075940
dc.contributor.referee2.fl_str_mv Lima, Rosemary Sousa Cunha
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/9097934027901875
dc.contributor.advisor1.fl_str_mv Damasceno, Bolívar Ponciano Goulart de Lima
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/6407334157973308
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/7441078028137833
dc.contributor.author.fl_str_mv Reis, Malu Maria Lucas dos
contributor_str_mv Machado, Giovanna
Lima, Rosemary Sousa Cunha
Damasceno, Bolívar Ponciano Goulart de Lima
dc.subject.eng.fl_str_mv Flavone
Nanoemulsion
Microemulsion
topic Flavone
Nanoemulsion
Microemulsion
CIENCIAS DA SAUDE
Microemulsão
Flavona
Nanoemulsão
dc.subject.cnpq.fl_str_mv CIENCIAS DA SAUDE
dc.subject.por.fl_str_mv Microemulsão
Flavona
Nanoemulsão
description Infectious diseases are responsible for about 25% deaths worldwide and 45% in underdeveloped countries. Antimicrobials are usually used to fight an established infection, they aim either to eliminate or to impede bacterial growth without causing harm to the patient. Flavone, a molecule derived from flavonoids, has evidence of bactericidal activity, with LogP of 3.37 which indicates high lipophilicity. Therefore, it needs a carrier system with lipophilic characteristics, such as microemulsions (ME) and nanoemulsions (NE) O/A, that are systems indicated to its incorporation and use as a novel drug delivery system (NDDS). The aim of this work was to develop nano/microemulsion systems for the incorporation of flavone, aiming topical application, characterizing them physico-chemically, defining a methodology for drug dosing. For the development of the systems and for the choice of formulations to be studied, the construction of the pseudo-ternary phase diagram was performed, followed by incorporation of the drug (1 mg/mL). From this, the physicochemical characterization of the samples was initiated: macroscopic evaluation, isotropy, pH measurement, refractive index, differential scanning calorimetry (DSC), transmission electron microscopy (MET), Zeta potential, droplet size and polydispersity index. In addition, the validation of an analytical method for flavone assay by UV-VIS spectrophotometer and high-performance liquid chromatography (HPLC) was performed. The NE developed was composed of 10.8% oil phase (isopropyl myristate), 25.87% surfactants (polyethylene glycol (15)-hydroxystearate/sorbitan monooleate 80) and 63.33% water. The ME has 34.5% oil phase, 34.5% surfactants and 31% water. Through isotropy, DSC and MET it was possible to prove that the nanoemulsion is O/A and the ME is a bicontinuous system. The analytical methods were validated, both linear, selective, accurate and robust. The present study was relevant for the area of pharmaceutical technology. We sought to develop novel systems with relevant therapeutic potential, since the proposed systems are unprecedented and the drug has the potential to treat antimicrobial diseases.
publishDate 2017
dc.date.issued.fl_str_mv 2017-02-16
dc.date.accessioned.fl_str_mv 2018-05-23T16:59:44Z
2026-02-27T10:27:46Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.citation.fl_str_mv REIS, M. M. L. dos. Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA). 2017. 69f. Dissertação (Programa de Pós-Graduação em Ciências Farmacêuticas - PPGCF) - Universidade Estadual da Paraíba, Campina Grande, 2017.
dc.identifier.uri.fl_str_mv https://repositorio.uepb.edu.br/handle/123456789/73287
dc.identifier.capesdegreeprogramcode.none.fl_str_mv 24004014014P8
identifier_str_mv REIS, M. M. L. dos. Sistemas nano/microemulsionados como carreadores para derivado flavonoídico (FLAVONA). 2017. 69f. Dissertação (Programa de Pós-Graduação em Ciências Farmacêuticas - PPGCF) - Universidade Estadual da Paraíba, Campina Grande, 2017.
24004014014P8
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