Filmes de polissacarídeos naturais para a veiculação cutânea de nanocápsulas de silibinina no tratamento da dermatite atópica

Detalhes bibliográficos
Ano de defesa: 2022
Autor(a) principal: Gehrcke, Mailine
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
dARK ID: ark:/26339/001300000ph0x
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Brasil
Desenvolvimento e Avaliação de Produtos Farmacêuticos
UFSM
Programa de Pós-Graduação em Ciências Farmacêuticas
Centro de Ciências da Saúde
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://repositorio.ufsm.br/handle/1/26348
Resumo: Current treatments for atopic dermatitis have restrictions adverse effects, and there is a need to develop therape due to the limited efficacy and pronounced utic alternatives. Thus, this study aimed to associate the potential of nanocapsules with the advantages provided by polymeric films, in order to develop a new topical formulation containing silibinin (SB), an antioxidant and anti flavonoid, finflammatory or atopic dermatitis treatment. The nanocapsule suspensions were prepared by the interfacial deposition method of the preformed polymer, using ethylcellulose and medium chain triglycerides, and showed nanometric size, polydispersity index below 0.2, negati ve zeta potential, acidic pH, SB content and encapsulation efficiency of about 100 %. Subsequently, these suspensions were incorporated into gellan gum films by the solvent deposition/evaporation method, using glycerol as plasticizer. For comparative purpo ses, vehicle films and films containing the nonnanoencapsulated flavonoid were also prepared. The developed films were thin, transparent, flexible and with swelling capacity greater than 100 %, remaining intact after 24 h in contact with pH 7.4 buffer. Th e film's irritation potential was evaluated by the chorioallantoic membrane test, which showed the formulations biocompatibility. Also, compared to films containing free SB, nanobased films showed greater occlusive property and better stability during st orage at room temperature. The in vitro release assay showed that the films containing the nanoencapsulated flavonoid had a controlled release profile, which is in agreement with the cutaneous permeation profile obtained. Despite the controlled release, it was possible to quantify therapeutic amounts of SB in the target layers for the skin diseases treatment (epidermis and dermis). In a second stage of the work, the feasibility of producing bilayer films of gellan gum/pullulan using the same preparation met hod was demonstrated. For this, a pullulan aqueous dispersion was cast onto the partially dried gellan gum layer containing nanocapsules. The bilayer films demonstrated a welltwolayer microstructure, which was evaluated by scanning electron micro defined scopy. Furthermore, the addition of the pullulan layer was able to give bioadhesive and less stiff characteristics to the films, as well as increasing their occlusive potential by about 2 times, without altering the profiles of release and cutaneous permea tion of SB. The antioxidant performance of the bilayer films containing silibinin nanocapsules was evaluated using the ABTS radical, which showed the high scavenger capacity of this flavonoid. It was also demonstrated that bilayer films are hemo/biocompati ble through a direct contact hemolysis assay. Finally, the biological performance of bilayer films was evaluated in an animal model of dinitrochlorobenzene induced atopic dermatitis. The association of SB nanocapsules into gellan/pullulan gum bilayer films attenuated dermatitislike lesions in mice, as well as modulating oxidative and inflammatory parameters. In conclusion, the incorporation of nanocapsules into gellan gum films provides greater stability and is able to control the skin release/permeation o f SB. Also, in the context of cutaneous application, the characteristics of these films can be improved by adding a pullulan layer, which is a novel and promising strategy for atopic dermatitis treatment.
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spelling Filmes de polissacarídeos naturais para a veiculação cutânea de nanocápsulas de silibinina no tratamento da dermatite atópicaNatural polysaccharide films for the cutaneous release of silibinin nanocapsules in the treatment of atopic dermatitisNanopartículasSilibininaFilmesPullulanGoma gelanaEczemasNanoparticlesSilibininFilmsPullulanGellan gumCNPQ::CIENCIAS DA SAUDE::FARMACIACurrent treatments for atopic dermatitis have restrictions adverse effects, and there is a need to develop therape due to the limited efficacy and pronounced utic alternatives. Thus, this study aimed to associate the potential of nanocapsules with the advantages provided by polymeric films, in order to develop a new topical formulation containing silibinin (SB), an antioxidant and anti flavonoid, finflammatory or atopic dermatitis treatment. The nanocapsule suspensions were prepared by the interfacial deposition method of the preformed polymer, using ethylcellulose and medium chain triglycerides, and showed nanometric size, polydispersity index below 0.2, negati ve zeta potential, acidic pH, SB content and encapsulation efficiency of about 100 %. Subsequently, these suspensions were incorporated into gellan gum films by the solvent deposition/evaporation method, using glycerol as plasticizer. For comparative purpo ses, vehicle films and films containing the nonnanoencapsulated flavonoid were also prepared. The developed films were thin, transparent, flexible and with swelling capacity greater than 100 %, remaining intact after 24 h in contact with pH 7.4 buffer. Th e film's irritation potential was evaluated by the chorioallantoic membrane test, which showed the formulations biocompatibility. Also, compared to films containing free SB, nanobased films showed greater occlusive property and better stability during st orage at room temperature. The in vitro release assay showed that the films containing the nanoencapsulated flavonoid had a controlled release profile, which is in agreement with the cutaneous permeation profile obtained. Despite the controlled release, it was possible to quantify therapeutic amounts of SB in the target layers for the skin diseases treatment (epidermis and dermis). In a second stage of the work, the feasibility of producing bilayer films of gellan gum/pullulan using the same preparation met hod was demonstrated. For this, a pullulan aqueous dispersion was cast onto the partially dried gellan gum layer containing nanocapsules. The bilayer films demonstrated a welltwolayer microstructure, which was evaluated by scanning electron micro defined scopy. Furthermore, the addition of the pullulan layer was able to give bioadhesive and less stiff characteristics to the films, as well as increasing their occlusive potential by about 2 times, without altering the profiles of release and cutaneous permea tion of SB. The antioxidant performance of the bilayer films containing silibinin nanocapsules was evaluated using the ABTS radical, which showed the high scavenger capacity of this flavonoid. It was also demonstrated that bilayer films are hemo/biocompati ble through a direct contact hemolysis assay. Finally, the biological performance of bilayer films was evaluated in an animal model of dinitrochlorobenzene induced atopic dermatitis. The association of SB nanocapsules into gellan/pullulan gum bilayer films attenuated dermatitislike lesions in mice, as well as modulating oxidative and inflammatory parameters. In conclusion, the incorporation of nanocapsules into gellan gum films provides greater stability and is able to control the skin release/permeation o f SB. Also, in the context of cutaneous application, the characteristics of these films can be improved by adding a pullulan layer, which is a novel and promising strategy for atopic dermatitis treatment.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESOs tratamentos atuais para dermatite atópica apresentam restrições devido à eficácia limitada e a efeitos adversos marcantes, havendo uma necessidade do desenvolvimento de alternativas terapêuticas. Assim, este estudo objetivou associar as potencialidades das nanocápsulas com as vantagens proporcionadas pelos filmes poliméricos, a fim de desenvolver uma nova formulação tópica contendo silibinina (SB), um flavonoide antioxidante e anti-inflamatório, para o tratamento da dermatite atópica. As suspensões de nanocápsulas foram preparadas pelo método de deposição interfacial do polímero pré-formado, utilizando etilcelulose e triglicerídeos de cadeia média, e demonstraram tamanho nanométrico, índice de polidispersão abaixo de 0,2, potencial zeta negativo, pH ácido, teor e eficiência de encapsulação de cerca de 100 %. Posteriormente, estas suspensões foram incorporadas em filmes de goma gelana pelo método de deposição/evaporação do solvente, utilizando glicerol como plastificante. Com fins comparativos foram também preparados filmes veículo e contendo o flavonoide não-nanoencapsulado. Os filmes desenvolvidos apresentaram-se finos, transparentes, flexíveis e com capacidade de intumescimento maior que 100 %, permanecendo intactos após 24 h em contato com o tampão pH 7,4. O potencial de irritação destes filmes foi avaliado pelo teste da membrana cório-alantóide que evidenciou a biocompatibilidade das formulações. Ainda, em comparação a filmes contendo a SB livre, os filmes de base nanotecnológica apresentaram maior propriedade oclusiva e melhor estabilidade durante o armazenamento em temperatura ambiente. O ensaio de liberação in vitro mostrou que os filmes contendo o flavonoide nanoencapsulado tiveram um perfil de liberação controlada, o que está de acordo com o perfil de permeação cutânea obtido. Apesar do controle de liberação, foi possível a quantificação de quantidades terapêuticas da SB nas camadas alvo para o tratamento de doenças da pele (epiderme e derme). Em uma segunda etapa do trabalho foi demonstrada a viabilidade de produção de filmes bicamada constituídos por goma gelana/pullulan utilizando o mesmo método de preparo. Para isto, uma dispersão de pullulan foi vertida sobre a camada de goma gelana e nanocápsulas parcialmente seca. Os filmes bicamada demonstraram microestrutura em duas camadas bem definidas, a qual foi avaliada por microscopia eletrônica de varredura. Ainda, a adição da camada de pullulan foi capaz de conferir bioadesividade e menor rigidez aos filmes, bem como aumentou em cerca de duas vezes o potencial oclusivo destes, sem alterar os perfis de liberação e permeação cutânea da SB. A performance antioxidante dos filmes bicamada foi avaliada utilizando o radical ABTS, que evidenciou a alta capacidade sequestrante do flavonoide. Foi também demonstrado que os filmes bicamada são hemo/biocompatíveis através de um ensaio in vitro de hemólise por contato direto. Por fim, foi avaliada a performance biológica dos filmes bicamada em um modelo animal de dermatite atópica induzida por dinitroclorobenzeno. A associação de nanocápsulas de SB em filmes bicamada de goma gelana/pullulan atenuou as lesões do tipo dermatite nos camundongos, bem como modulou parâmetros oxidativos e inflamatórios. Como conclusão, a combinação de nanocápsulas em filmes de goma gelana possibilita maior estabilidade e é capaz de controlar a liberação/permeação cutânea da SB. Ainda, no contexto da aplicação cutânea, as características destes filmes podem ser aprimoradas através da adição de uma camada de pullulan, sendo esta uma nova e promissora estratégia para o tratamento da dermatite atópicaUniversidade Federal de Santa MariaBrasilDesenvolvimento e Avaliação de Produtos FarmacêuticosUFSMPrograma de Pós-Graduação em Ciências FarmacêuticasCentro de Ciências da SaúdeCruz, Letíciahttp://lattes.cnpq.br/3095970241017527Adams, Andréa Inês HornOurique, Aline FerreiraSilva, Cristiane de Bona daGuterres, Silvia StanisçuaskiGehrcke, Mailine2022-10-04T19:26:47Z2022-10-04T19:26:47Z2022-08-29info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/26348ark:/26339/001300000ph0xporAttribution-NonCommercial-NoDerivatives 4.0 Internationalinfo:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2022-10-04T19:26:48Zoai:repositorio.ufsm.br:1/26348Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/PUBhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.com||manancial@ufsm.bropendoar:2022-10-04T19:26:48Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Filmes de polissacarídeos naturais para a veiculação cutânea de nanocápsulas de silibinina no tratamento da dermatite atópica
Natural polysaccharide films for the cutaneous release of silibinin nanocapsules in the treatment of atopic dermatitis
title Filmes de polissacarídeos naturais para a veiculação cutânea de nanocápsulas de silibinina no tratamento da dermatite atópica
spellingShingle Filmes de polissacarídeos naturais para a veiculação cutânea de nanocápsulas de silibinina no tratamento da dermatite atópica
Gehrcke, Mailine
Nanopartículas
Silibinina
Filmes
Pullulan
Goma gelana
Eczemas
Nanoparticles
Silibinin
Films
Pullulan
Gellan gum
CNPQ::CIENCIAS DA SAUDE::FARMACIA
title_short Filmes de polissacarídeos naturais para a veiculação cutânea de nanocápsulas de silibinina no tratamento da dermatite atópica
title_full Filmes de polissacarídeos naturais para a veiculação cutânea de nanocápsulas de silibinina no tratamento da dermatite atópica
title_fullStr Filmes de polissacarídeos naturais para a veiculação cutânea de nanocápsulas de silibinina no tratamento da dermatite atópica
title_full_unstemmed Filmes de polissacarídeos naturais para a veiculação cutânea de nanocápsulas de silibinina no tratamento da dermatite atópica
title_sort Filmes de polissacarídeos naturais para a veiculação cutânea de nanocápsulas de silibinina no tratamento da dermatite atópica
author Gehrcke, Mailine
author_facet Gehrcke, Mailine
author_role author
dc.contributor.none.fl_str_mv Cruz, Letícia
http://lattes.cnpq.br/3095970241017527
Adams, Andréa Inês Horn
Ourique, Aline Ferreira
Silva, Cristiane de Bona da
Guterres, Silvia Stanisçuaski
dc.contributor.author.fl_str_mv Gehrcke, Mailine
dc.subject.por.fl_str_mv Nanopartículas
Silibinina
Filmes
Pullulan
Goma gelana
Eczemas
Nanoparticles
Silibinin
Films
Pullulan
Gellan gum
CNPQ::CIENCIAS DA SAUDE::FARMACIA
topic Nanopartículas
Silibinina
Filmes
Pullulan
Goma gelana
Eczemas
Nanoparticles
Silibinin
Films
Pullulan
Gellan gum
CNPQ::CIENCIAS DA SAUDE::FARMACIA
description Current treatments for atopic dermatitis have restrictions adverse effects, and there is a need to develop therape due to the limited efficacy and pronounced utic alternatives. Thus, this study aimed to associate the potential of nanocapsules with the advantages provided by polymeric films, in order to develop a new topical formulation containing silibinin (SB), an antioxidant and anti flavonoid, finflammatory or atopic dermatitis treatment. The nanocapsule suspensions were prepared by the interfacial deposition method of the preformed polymer, using ethylcellulose and medium chain triglycerides, and showed nanometric size, polydispersity index below 0.2, negati ve zeta potential, acidic pH, SB content and encapsulation efficiency of about 100 %. Subsequently, these suspensions were incorporated into gellan gum films by the solvent deposition/evaporation method, using glycerol as plasticizer. For comparative purpo ses, vehicle films and films containing the nonnanoencapsulated flavonoid were also prepared. The developed films were thin, transparent, flexible and with swelling capacity greater than 100 %, remaining intact after 24 h in contact with pH 7.4 buffer. Th e film's irritation potential was evaluated by the chorioallantoic membrane test, which showed the formulations biocompatibility. Also, compared to films containing free SB, nanobased films showed greater occlusive property and better stability during st orage at room temperature. The in vitro release assay showed that the films containing the nanoencapsulated flavonoid had a controlled release profile, which is in agreement with the cutaneous permeation profile obtained. Despite the controlled release, it was possible to quantify therapeutic amounts of SB in the target layers for the skin diseases treatment (epidermis and dermis). In a second stage of the work, the feasibility of producing bilayer films of gellan gum/pullulan using the same preparation met hod was demonstrated. For this, a pullulan aqueous dispersion was cast onto the partially dried gellan gum layer containing nanocapsules. The bilayer films demonstrated a welltwolayer microstructure, which was evaluated by scanning electron micro defined scopy. Furthermore, the addition of the pullulan layer was able to give bioadhesive and less stiff characteristics to the films, as well as increasing their occlusive potential by about 2 times, without altering the profiles of release and cutaneous permea tion of SB. The antioxidant performance of the bilayer films containing silibinin nanocapsules was evaluated using the ABTS radical, which showed the high scavenger capacity of this flavonoid. It was also demonstrated that bilayer films are hemo/biocompati ble through a direct contact hemolysis assay. Finally, the biological performance of bilayer films was evaluated in an animal model of dinitrochlorobenzene induced atopic dermatitis. The association of SB nanocapsules into gellan/pullulan gum bilayer films attenuated dermatitislike lesions in mice, as well as modulating oxidative and inflammatory parameters. In conclusion, the incorporation of nanocapsules into gellan gum films provides greater stability and is able to control the skin release/permeation o f SB. Also, in the context of cutaneous application, the characteristics of these films can be improved by adding a pullulan layer, which is a novel and promising strategy for atopic dermatitis treatment.
publishDate 2022
dc.date.none.fl_str_mv 2022-10-04T19:26:47Z
2022-10-04T19:26:47Z
2022-08-29
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/26348
dc.identifier.dark.fl_str_mv ark:/26339/001300000ph0x
url http://repositorio.ufsm.br/handle/1/26348
identifier_str_mv ark:/26339/001300000ph0x
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Desenvolvimento e Avaliação de Produtos Farmacêuticos
UFSM
Programa de Pós-Graduação em Ciências Farmacêuticas
Centro de Ciências da Saúde
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Desenvolvimento e Avaliação de Produtos Farmacêuticos
UFSM
Programa de Pós-Graduação em Ciências Farmacêuticas
Centro de Ciências da Saúde
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com||manancial@ufsm.br
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