Desenvolvimento tecnológico de supositórios vaginais contendo nanopartículas poliméricas de tioconazol

Detalhes bibliográficos
Ano de defesa: 2015
Autor(a) principal: Cossetin, Luciana Filippin lattes
Orientador(a): Silva, Cristiane de Bona da lattes
Banca de defesa: Ourique, Aline Ferreira lattes, Canto, Gizele Scotti do lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Centro de Ciências da Saúde
Programa de Pós-Graduação: Programa de Pós-Graduação em Ciências Farmacêuticas
Departamento: Farmácia
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufsm.br/handle/1/17533
Resumo: The development of nanostructured materials has provided better control of the release and targeting of active substances to the treatment site, minimizing adverse effects, in addition to contributing to increased therapeutic efficacy. In this sense, these carriers are an alternative for the development of products administered by vaginal route because the pharmaceutical forms commonly used promote inadequate distribution and penetration of drugs, in addition to the reduced time spent on site. Therefore, this study aimed to develop vaginal suppositories containing dried products prepared from polymeric nanoparticle suspensions containing tioconazole, an antifungal used to treat vulvovaginitis. Suspensions of polymeric nanospheres and nanocapsules containing tioconazole (3 mg / ml) were prepared and evaluated for average particle diameter (166-203 nm) polydispersion index (less than 0.20), negative zeta potential (6 - 10 mV), pH (weakly acidic), drug content (value close to the theoretical) and encapsulation efficiency (approximately 100%), which were adequate and stable over the period of 30 days. After the suspensions were subjected to spray drying to obtain the solid intermediates, which were characterized in relation to the weight yield of resuspending in water content profile of particle size distribution, drug content, humidity and morphology. Regarding these characteristics, the results were satisfactory: yield weight, approximately 60%, drug content close to the theoretical value (21 mg / g), resuspending ratio close to unity and maintenance of submicrometric particle size. These characteristics have remained after 30 days of storage at room temperature, only dried products containing the nanospheres. Subsequently, the dried products were incorporated into a gelatin-glycerin base to obtain vaginal suppositories. All formulations had surface characteristics and homogeneous dimensions; drug content close to the theoretical concentration (23 mg / suppository); average weight between 4.51 and 4.57 g; content uniformity and disintegration time less than 60 minutes. Suppositories consisting of the nanospheres enabled greater control of the release of tioconazole compared with suppositories containing the drug not associated. Thus, the formulations proposed in this work may constitute an alternative for the administration by vaginal route tioconazole, better acceptability compared to the existing dosage forms (creams, gels) enabling, by definition, a greater therapeutic effect of the drug in order the advantages that nanotechnology presents.
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spelling 2019-07-22T21:14:01Z2019-07-22T21:14:01Z2015-08-14http://repositorio.ufsm.br/handle/1/17533The development of nanostructured materials has provided better control of the release and targeting of active substances to the treatment site, minimizing adverse effects, in addition to contributing to increased therapeutic efficacy. In this sense, these carriers are an alternative for the development of products administered by vaginal route because the pharmaceutical forms commonly used promote inadequate distribution and penetration of drugs, in addition to the reduced time spent on site. Therefore, this study aimed to develop vaginal suppositories containing dried products prepared from polymeric nanoparticle suspensions containing tioconazole, an antifungal used to treat vulvovaginitis. Suspensions of polymeric nanospheres and nanocapsules containing tioconazole (3 mg / ml) were prepared and evaluated for average particle diameter (166-203 nm) polydispersion index (less than 0.20), negative zeta potential (6 - 10 mV), pH (weakly acidic), drug content (value close to the theoretical) and encapsulation efficiency (approximately 100%), which were adequate and stable over the period of 30 days. After the suspensions were subjected to spray drying to obtain the solid intermediates, which were characterized in relation to the weight yield of resuspending in water content profile of particle size distribution, drug content, humidity and morphology. Regarding these characteristics, the results were satisfactory: yield weight, approximately 60%, drug content close to the theoretical value (21 mg / g), resuspending ratio close to unity and maintenance of submicrometric particle size. These characteristics have remained after 30 days of storage at room temperature, only dried products containing the nanospheres. Subsequently, the dried products were incorporated into a gelatin-glycerin base to obtain vaginal suppositories. All formulations had surface characteristics and homogeneous dimensions; drug content close to the theoretical concentration (23 mg / suppository); average weight between 4.51 and 4.57 g; content uniformity and disintegration time less than 60 minutes. Suppositories consisting of the nanospheres enabled greater control of the release of tioconazole compared with suppositories containing the drug not associated. Thus, the formulations proposed in this work may constitute an alternative for the administration by vaginal route tioconazole, better acceptability compared to the existing dosage forms (creams, gels) enabling, by definition, a greater therapeutic effect of the drug in order the advantages that nanotechnology presents.O desenvolvimento de sistemas nanoestruturados tem proporcionado melhor controle da liberação e o direcionamento de substâncias ativas ao local terapêutico, minimizando, assim, efeitos adversos, além de contribuir para o aumento da eficácia terapêutica. Neste sentido, esses carreadores constituem uma alternativa para o desenvolvimento de produtos administrados pela via vaginal, pois as formas farmacêuticas comumente utilizadas promovem distribuição e penetração inadequadas dos fármacos, além do reduzido tempo de permanência no local. Com isso, este trabalho teve por objetivo desenvolver supositórios vaginais contendo produtos secos preparados a partir de suspensões de nanopartículas poliméricas contendo tioconazol, um antifúngico utilizado no tratamento de vulvovaginites. As suspensões de nanoesferas e nanocápsulas poliméricas contendo tioconazol (3 mg/mL) foram preparadas pela técnica da nanoprecipitação e avaliadas quanto ao diâmetro médio de partículas (166 – 203 nm), índice de polidispersão (inferior a 0,20), potencial zeta negativo (6 – 10 mV), pH (fracamente ácido), teor de fármaco (próximo ao teórico) e eficiência de encapsulamento (aproximadamente 100%), as quais foram adequadas e estáveis durante o período de 30 dias sob condições de temperatura ambiente. Após a preparação, as suspensões foram submetidas à secagem por aspersão para a obtenção dos produtos sólidos intermediários, os quais foram caracterizados em relação ao rendimento ponderal, índice de ressuspensão em água, perfil de distribuição de tamanho de partículas, teor de fármaco, umidade e morfologia. Quanto a essas características, os resultados foram satisfatórios: rendimento ponderal de, aproximadamente, 60%, conteúdo de fármaco próximo do valor teórico (21 mg/g), índice de ressuspensão próximo a unidade e recuperação do tamanho submicrométrico das partículas. Essas características mantiveram-se, após 30 dias de armazenamento a temperatura ambiente, somente para os produtos secos contendo as nanoesferas. Posteriormente, os produtos secos foram incorporados em uma base de gelatina-glicerina a fim de obter supositórios vaginais. Todas as formulações apresentaram características de superfície e de dimensões homogêneas; teor de fármaco próximo da concentração teórica (23 mg/supositório); peso médio entre 4,51 e 4,57 g; uniformidade de conteúdo e tempo de desintegração inferior a 60 minutos. Os supositórios constituídos pelas nanoesferas possibilitaram um maior controle da liberação do tioconazol em comparação aos supositórios contendo o fármaco não associado. Dessa forma, as formulações propostas neste trabalho poderão constituir uma alternativa para a administração do tioconazol pela via vaginal, de melhor aceitabilidade face às formas farmacêuticas já existentes (cremes, géis) possibilitando, por hipótese, um maior efeito terapêutico do fármaco, tendo em vista as vantagens que a nanotecnologia apresenta.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESporUniversidade Federal de Santa MariaCentro de Ciências da SaúdePrograma de Pós-Graduação em Ciências FarmacêuticasUFSMBrasilFarmáciaAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessNanopartículas poliméricasTioconazolProdutos sólidosSupositórios vaginaisSpray-dryingPolymeric nanoparticlesNanospheresDry productsVaginal suppositoriesCNPQ::CIENCIAS DA SAUDE::FARMACIADesenvolvimento tecnológico de supositórios vaginais contendo nanopartículas poliméricas de tioconazolTechnological development of vaginal suppositories containing polymeric nanoparticles of tioconazoleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisSilva, Cristiane de Bona dahttp://lattes.cnpq.br/6029111646602279Ourique, Aline Ferreirahttp://lattes.cnpq.br/7478810804464054Canto, Gizele Scotti dohttp://lattes.cnpq.br/2076175621657265http://lattes.cnpq.br/0376380448241174Cossetin, Luciana Filippin40030000000560077eeaef8-05f4-4cee-b949-c09342e7eb61fdd8ae3e-49d9-4339-810a-c8f8050b5e98dd172234-8fdf-4467-8031-137b919d3f99526f2155-c289-4a9a-ab68-611b482916dereponame:Biblioteca Digital de Teses e Dissertações do UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALDIS_PPGCF_2015_COSSETIN_LUCIANA.pdfDIS_PPGCF_2015_COSSETIN_LUCIANA.pdfDissertação de Mestradoapplication/pdf1291591http://repositorio.ufsm.br/bitstream/1/17533/1/DIS_PPGCF_2015_COSSETIN_LUCIANA.pdf430f4d79ba0bfd4720f00176bdf6ea16MD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; 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dc.title.por.fl_str_mv Desenvolvimento tecnológico de supositórios vaginais contendo nanopartículas poliméricas de tioconazol
dc.title.alternative.eng.fl_str_mv Technological development of vaginal suppositories containing polymeric nanoparticles of tioconazole
title Desenvolvimento tecnológico de supositórios vaginais contendo nanopartículas poliméricas de tioconazol
spellingShingle Desenvolvimento tecnológico de supositórios vaginais contendo nanopartículas poliméricas de tioconazol
Cossetin, Luciana Filippin
Nanopartículas poliméricas
Tioconazol
Produtos sólidos
Supositórios vaginais
Spray-drying
Polymeric nanoparticles
Nanospheres
Dry products
Vaginal suppositories
CNPQ::CIENCIAS DA SAUDE::FARMACIA
title_short Desenvolvimento tecnológico de supositórios vaginais contendo nanopartículas poliméricas de tioconazol
title_full Desenvolvimento tecnológico de supositórios vaginais contendo nanopartículas poliméricas de tioconazol
title_fullStr Desenvolvimento tecnológico de supositórios vaginais contendo nanopartículas poliméricas de tioconazol
title_full_unstemmed Desenvolvimento tecnológico de supositórios vaginais contendo nanopartículas poliméricas de tioconazol
title_sort Desenvolvimento tecnológico de supositórios vaginais contendo nanopartículas poliméricas de tioconazol
author Cossetin, Luciana Filippin
author_facet Cossetin, Luciana Filippin
author_role author
dc.contributor.advisor1.fl_str_mv Silva, Cristiane de Bona da
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/6029111646602279
dc.contributor.referee1.fl_str_mv Ourique, Aline Ferreira
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/7478810804464054
dc.contributor.referee2.fl_str_mv Canto, Gizele Scotti do
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/2076175621657265
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/0376380448241174
dc.contributor.author.fl_str_mv Cossetin, Luciana Filippin
contributor_str_mv Silva, Cristiane de Bona da
Ourique, Aline Ferreira
Canto, Gizele Scotti do
dc.subject.por.fl_str_mv Nanopartículas poliméricas
Tioconazol
Produtos sólidos
Supositórios vaginais
topic Nanopartículas poliméricas
Tioconazol
Produtos sólidos
Supositórios vaginais
Spray-drying
Polymeric nanoparticles
Nanospheres
Dry products
Vaginal suppositories
CNPQ::CIENCIAS DA SAUDE::FARMACIA
dc.subject.eng.fl_str_mv Spray-drying
Polymeric nanoparticles
Nanospheres
Dry products
Vaginal suppositories
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS DA SAUDE::FARMACIA
description The development of nanostructured materials has provided better control of the release and targeting of active substances to the treatment site, minimizing adverse effects, in addition to contributing to increased therapeutic efficacy. In this sense, these carriers are an alternative for the development of products administered by vaginal route because the pharmaceutical forms commonly used promote inadequate distribution and penetration of drugs, in addition to the reduced time spent on site. Therefore, this study aimed to develop vaginal suppositories containing dried products prepared from polymeric nanoparticle suspensions containing tioconazole, an antifungal used to treat vulvovaginitis. Suspensions of polymeric nanospheres and nanocapsules containing tioconazole (3 mg / ml) were prepared and evaluated for average particle diameter (166-203 nm) polydispersion index (less than 0.20), negative zeta potential (6 - 10 mV), pH (weakly acidic), drug content (value close to the theoretical) and encapsulation efficiency (approximately 100%), which were adequate and stable over the period of 30 days. After the suspensions were subjected to spray drying to obtain the solid intermediates, which were characterized in relation to the weight yield of resuspending in water content profile of particle size distribution, drug content, humidity and morphology. Regarding these characteristics, the results were satisfactory: yield weight, approximately 60%, drug content close to the theoretical value (21 mg / g), resuspending ratio close to unity and maintenance of submicrometric particle size. These characteristics have remained after 30 days of storage at room temperature, only dried products containing the nanospheres. Subsequently, the dried products were incorporated into a gelatin-glycerin base to obtain vaginal suppositories. All formulations had surface characteristics and homogeneous dimensions; drug content close to the theoretical concentration (23 mg / suppository); average weight between 4.51 and 4.57 g; content uniformity and disintegration time less than 60 minutes. Suppositories consisting of the nanospheres enabled greater control of the release of tioconazole compared with suppositories containing the drug not associated. Thus, the formulations proposed in this work may constitute an alternative for the administration by vaginal route tioconazole, better acceptability compared to the existing dosage forms (creams, gels) enabling, by definition, a greater therapeutic effect of the drug in order the advantages that nanotechnology presents.
publishDate 2015
dc.date.issued.fl_str_mv 2015-08-14
dc.date.accessioned.fl_str_mv 2019-07-22T21:14:01Z
dc.date.available.fl_str_mv 2019-07-22T21:14:01Z
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url http://repositorio.ufsm.br/handle/1/17533
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dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
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rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências da Saúde
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Ciências Farmacêuticas
dc.publisher.initials.fl_str_mv UFSM
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Farmácia
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências da Saúde
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