Hidrogel de base nanotecnológica contendo silibinina com ação anti-inflamatória no modelo de óleo de cróton

Detalhes bibliográficos
Ano de defesa: 2018
Autor(a) principal: Rigon, Cristina lattes
Orientador(a): Cruz, Letícia lattes
Banca de defesa: Nogueira, Cristina Wayne, Paese, Karina
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: Análises Clínicas e Toxicológicas
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufsm.br/handle/1/20985
Resumo: Currently, irritant contact dermatitis is the most prevalent dermatitis among the others and is triggered by the activation of innate immunity after skin contact with irritants. Silibinin (SB), a naturally occurring active, has beneficial activities for the cutaneous tissue, among which the anti-inflammatory action can be highlighted. Thus, in studies conducted in our research group, nanocapsule suspensions containing pomegranate oil as oily core and silibinin as active have been developed. Aiming at the skin application, this dissertation aimed to develop an innovative bioadhesive hydrogel for the delivery of this NC suspension and to verify its potential in the treatment of irritative contact dermatitis. The hydrogel was prepared from the polymer Pemulen® TR2, which has bioadhesive characteristics. The formulations were characterized in terms of SB content, pH, particle size and distribution, as well as spreadability and rheology, important characteristics mainly in the development of new products for dermal administration. For the studies of SB release from the hydrogels and cutaneous permeation of the active in human skin Franz cells were used. The bioadhesiveness test was performed using a texturometer and, in order to guarantee the safety of the formulations, the cutaneous biometry assay was performed, evaluating the parameters of erythema, pH, transepidermal loss of water and skin hydration. Also, considering the ability of SB to regulate inflammatory events, the viability of these hydrogels in the inflammation treatment was studied in an animal model induced by croton oil. The proposed formulations presented physico-chemical characteristics compatible with topical administration, maintaining the nanometric size after incorporation into the hydrogels (184 ± 26 nm), adequate pH range (6.70 ± 0.15), SB concentration close to concentration (0.99 ± 0.01 mg/g), as well as non-Newtonian pseudoplastic behavior. The in vitro release evidenced that the hydrogels containing the nanocapsules provided less silibinin retention in the dosage form for both media: phosphate buffer pH 5.5 plus ethanol and the buffer alone (4.73 ± 0.50 μg / mL for HP-NCSB and 1.14 ± 0.18 μg/mL for HP-SB and 2.25 ± 0.25 μg/mL from HP-NCSB and 0.49 ± 0.05 μg/mL for HP-SB, respectively). Permeation studies on human skin have indicated that the nanoencapsulation of silibinin increases its retention in the stratum corneum, which can act as a deposit for gradual release of this active. Evaluating the bioadhesive potential of the formulations, it was verified that the HP-NCSB stands out against the other formulations tested. In the in vivo study, the hydrogels containing the silibinin nanocapsules and pomegranate oil were able to act by expressively reducing ear edema and inflammatory cells. In the cutaneous biometry test, for all the parameters tested the formulations did not alter the normal skin conditions of the volunteers. Therefore, based on the results obtained, the hydrogel development was successful and the formulation has met the proposed therapeutic purpose, and may be a therapeutic alternative for the treatment of irritant contact dermatitis, using the natural source active silibinin allied to nanotechnology, since it was possible to demonstrate that the hydrogel containing silibinin nanocapsules had satisfactory results against the hydrogel containing non-nanoencapsulated silibinin, as well as it was possible to demonstrate the contribution of Pemulen® TR2 in the performance of the formulations.
id UFSM-20_a155751f2a9e8efd5cd315d92f71859e
oai_identifier_str oai:repositorio.ufsm.br:1/20985
network_acronym_str UFSM-20
network_name_str Manancial - Repositório Digital da UFSM
repository_id_str
spelling 2021-05-25T19:12:55Z2021-05-25T19:12:55Z2018-11-30http://repositorio.ufsm.br/handle/1/20985Currently, irritant contact dermatitis is the most prevalent dermatitis among the others and is triggered by the activation of innate immunity after skin contact with irritants. Silibinin (SB), a naturally occurring active, has beneficial activities for the cutaneous tissue, among which the anti-inflammatory action can be highlighted. Thus, in studies conducted in our research group, nanocapsule suspensions containing pomegranate oil as oily core and silibinin as active have been developed. Aiming at the skin application, this dissertation aimed to develop an innovative bioadhesive hydrogel for the delivery of this NC suspension and to verify its potential in the treatment of irritative contact dermatitis. The hydrogel was prepared from the polymer Pemulen® TR2, which has bioadhesive characteristics. The formulations were characterized in terms of SB content, pH, particle size and distribution, as well as spreadability and rheology, important characteristics mainly in the development of new products for dermal administration. For the studies of SB release from the hydrogels and cutaneous permeation of the active in human skin Franz cells were used. The bioadhesiveness test was performed using a texturometer and, in order to guarantee the safety of the formulations, the cutaneous biometry assay was performed, evaluating the parameters of erythema, pH, transepidermal loss of water and skin hydration. Also, considering the ability of SB to regulate inflammatory events, the viability of these hydrogels in the inflammation treatment was studied in an animal model induced by croton oil. The proposed formulations presented physico-chemical characteristics compatible with topical administration, maintaining the nanometric size after incorporation into the hydrogels (184 ± 26 nm), adequate pH range (6.70 ± 0.15), SB concentration close to concentration (0.99 ± 0.01 mg/g), as well as non-Newtonian pseudoplastic behavior. The in vitro release evidenced that the hydrogels containing the nanocapsules provided less silibinin retention in the dosage form for both media: phosphate buffer pH 5.5 plus ethanol and the buffer alone (4.73 ± 0.50 μg / mL for HP-NCSB and 1.14 ± 0.18 μg/mL for HP-SB and 2.25 ± 0.25 μg/mL from HP-NCSB and 0.49 ± 0.05 μg/mL for HP-SB, respectively). Permeation studies on human skin have indicated that the nanoencapsulation of silibinin increases its retention in the stratum corneum, which can act as a deposit for gradual release of this active. Evaluating the bioadhesive potential of the formulations, it was verified that the HP-NCSB stands out against the other formulations tested. In the in vivo study, the hydrogels containing the silibinin nanocapsules and pomegranate oil were able to act by expressively reducing ear edema and inflammatory cells. In the cutaneous biometry test, for all the parameters tested the formulations did not alter the normal skin conditions of the volunteers. Therefore, based on the results obtained, the hydrogel development was successful and the formulation has met the proposed therapeutic purpose, and may be a therapeutic alternative for the treatment of irritant contact dermatitis, using the natural source active silibinin allied to nanotechnology, since it was possible to demonstrate that the hydrogel containing silibinin nanocapsules had satisfactory results against the hydrogel containing non-nanoencapsulated silibinin, as well as it was possible to demonstrate the contribution of Pemulen® TR2 in the performance of the formulations.Atualmente, a dermatite de contato irritativa é a dermatite mais prevalente entre as demais e é desencadeada pela ativação da imunidade inata, após o contato da pele com agentes irritantes. A silibinina (SB), um ativo de ocorrência natural, apresenta atividades benéficas para o tecido cutâneo, dentre as quais pode-se destacar a ação anti-inflamatória. Desta forma, em estudos realizados no nosso grupo de pesquisa, foram desenvolvidas suspensões de nanocápsulas contendo óleo de romã como núcleo oleoso e silibinina como ativo. Visando a aplicação na pele, esta dissertação objetivou desenvolver um hidrogel bioadesivo inovador para a veiculação desta suspensão de NC e verificar seu potencial no tratamento da dermatite de contato irritativa. O hidrogel foi preparado a partir do polímero Pemulen® TR2, que apresenta características bioadesivas. As formulações foram caracterizadas quanto ao teor de SB, pH, tamanho e distribuição das partículas, bem como espalhabilidade e reologia, características importantes principalmente no desenvolvimento de novos produtos para administração cutânea. Para os estudos de liberação da SB a partir dos hidrogéis e permeação cutânea do ativo em pele humana utilizou-se células de Franz. O teste de bioadesividade foi realizado utilizando um texturômetro e, visando garantir a segurança das formulações, o ensaio de biometria cutânea foi executado, avaliando-se os parâmetros de eritema, pH, perda transepidermal de água e hidratação cutânea. Ainda, considerando a capacidade da SB em regular eventos inflamatórios, estudou-se a viabilidade destes hidrogéis no tratamento da inflamação em um modelo animal induzido por óleo de cróton. A formulação proposta apresentou características físico-químicas compatíveis com a administração tópica, mantendo o tamanho nanométrico após a incorporação nos hidrogéis (184 ± 26 nm), faixa de pH adequada (6,70 ± 0,15), concentração de SB próxima a concentração teórica (0,99±0,01 mg/g), assim como comportamento não-newtoniano pseudoplástico. A liberação in vitro evidenciou que os hidrogéis que continham as nanocápsulas proporcionaram uma menor retenção da silibinina na forma farmacêutica tanto para o meio contendo tampão fosfato pH 5,5 acrescido de etanol como para o meio apenas com tampão (4,73 ± 0,50 µg/mL para o HP-NCSB e 1,14 ± 0,18 µg/mL para o HP-SB e 2,25 ± 0,25 µg/mL a partir do HP-NCSB e 0,49 ± 0,05 µg/mL para o HP-SB, respectivamente). Os estudos de permeação em pele humana indicaram que a nanoencapsulação da silibinina aumenta sua retenção no estrato córneo, o que pode funcionar como depósito para liberação gradual deste ativo. Avaliando-se o potencial bioadesivo das formulações, constatou-se que o HP- NCSB destaca-se frente as demais formulações testadas. No estudo in vivo, os hidrogéis contendo as nanocápsulas de silibinina e óleo de romã foram capazes de atuar reduzindo expressivamente o edema de orelha e as células inflamatórias. No ensaio de biometria cutânea, para todos os parâmetros testados as formulações não alteraram as condições normais da pele dos voluntários. Portanto, baseado nos resultados obtidos, o desenvolvimento do hidrogel foi bem sucedido e que este atendeu a finalidade terapêutica proposta, podendo ser uma alternativa terapêutica para o tratamento da dermatite de contato irritativa, utilizando o ativo de origem natural silibinina aliado a nanotecnologia, uma vez que foi possível demonstrar que o hidrogel contendo nanocápsulas de silibinina teve resultados satisfatórios frente ao hidrogel contendo silibinina não-nanoencapsulada, assim como foi possível demonstrar a contribuição do Pemulen® TR2 no desempenho das formulações.porUniversidade Federal de Santa MariaCentro de Ciências da SaúdePrograma de Pós-Graduação em Ciências FarmacêuticasUFSMBrasilAnálises Clínicas e ToxicológicasAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessSemissólidosNanopartículasSilimarinaInflamaçãoSemisolidsNanoparticlesSilymarinInflammationCNPQ::CIENCIAS DA SAUDE::FARMACIAHidrogel de base nanotecnológica contendo silibinina com ação anti-inflamatória no modelo de óleo de crótonNanotechnology-based hydrogels containing silibinin with anti- inflammatory action in crotton oil modelinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisCruz, Letíciahttp://lattes.cnpq.br/3095970241017527Nogueira, Cristina WaynePaese, Karinahttp://lattes.cnpq.br/0048655224986199Rigon, Cristina400300000005600087e54fa-1802-4e8a-a314-a3ffa14190d988edf2f5-2ce3-436f-a4b2-2565a2fd22fc1e373fcc-89bd-4103-adba-676f6dcec787d4467822-0fe5-4124-912e-ddd78a6dc0fbreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALDIS_PPGCF_2018_RIGON_CRISTINA.pdfDIS_PPGCF_2018_RIGON_CRISTINA.pdfDissertação de Mestradoapplication/pdf2052693http://repositorio.ufsm.br/bitstream/1/20985/1/DIS_PPGCF_2018_RIGON_CRISTINA.pdfee2f5d311a17e4827e8702f40a72c60aMD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8805http://repositorio.ufsm.br/bitstream/1/20985/2/license_rdf4460e5956bc1d1639be9ae6146a50347MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81956http://repositorio.ufsm.br/bitstream/1/20985/3/license.txt2f0571ecee68693bd5cd3f17c1e075dfMD53TEXTDIS_PPGCF_2018_RIGON_CRISTINA.pdf.txtDIS_PPGCF_2018_RIGON_CRISTINA.pdf.txtExtracted texttext/plain251749http://repositorio.ufsm.br/bitstream/1/20985/4/DIS_PPGCF_2018_RIGON_CRISTINA.pdf.txt57282fd1a0fa1ad21e0f4b765f9fcba5MD54THUMBNAILDIS_PPGCF_2018_RIGON_CRISTINA.pdf.jpgDIS_PPGCF_2018_RIGON_CRISTINA.pdf.jpgIM Thumbnailimage/jpeg4542http://repositorio.ufsm.br/bitstream/1/20985/5/DIS_PPGCF_2018_RIGON_CRISTINA.pdf.jpg05bff5d43768ccf0ca8648eb2a23231cMD551/209852022-10-06 17:00:34.293oai:repositorio.ufsm.br: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ório Institucionalhttp://repositorio.ufsm.br/PUBhttp://repositorio.ufsm.br/oai/requestopendoar:39132022-10-06T20:00:34Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.por.fl_str_mv Hidrogel de base nanotecnológica contendo silibinina com ação anti-inflamatória no modelo de óleo de cróton
dc.title.alternative.eng.fl_str_mv Nanotechnology-based hydrogels containing silibinin with anti- inflammatory action in crotton oil model
title Hidrogel de base nanotecnológica contendo silibinina com ação anti-inflamatória no modelo de óleo de cróton
spellingShingle Hidrogel de base nanotecnológica contendo silibinina com ação anti-inflamatória no modelo de óleo de cróton
Rigon, Cristina
Semissólidos
Nanopartículas
Silimarina
Inflamação
Semisolids
Nanoparticles
Silymarin
Inflammation
CNPQ::CIENCIAS DA SAUDE::FARMACIA
title_short Hidrogel de base nanotecnológica contendo silibinina com ação anti-inflamatória no modelo de óleo de cróton
title_full Hidrogel de base nanotecnológica contendo silibinina com ação anti-inflamatória no modelo de óleo de cróton
title_fullStr Hidrogel de base nanotecnológica contendo silibinina com ação anti-inflamatória no modelo de óleo de cróton
title_full_unstemmed Hidrogel de base nanotecnológica contendo silibinina com ação anti-inflamatória no modelo de óleo de cróton
title_sort Hidrogel de base nanotecnológica contendo silibinina com ação anti-inflamatória no modelo de óleo de cróton
author Rigon, Cristina
author_facet Rigon, Cristina
author_role author
dc.contributor.advisor1.fl_str_mv Cruz, Letícia
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/3095970241017527
dc.contributor.referee1.fl_str_mv Nogueira, Cristina Wayne
dc.contributor.referee2.fl_str_mv Paese, Karina
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/0048655224986199
dc.contributor.author.fl_str_mv Rigon, Cristina
contributor_str_mv Cruz, Letícia
Nogueira, Cristina Wayne
Paese, Karina
dc.subject.por.fl_str_mv Semissólidos
Nanopartículas
Silimarina
Inflamação
topic Semissólidos
Nanopartículas
Silimarina
Inflamação
Semisolids
Nanoparticles
Silymarin
Inflammation
CNPQ::CIENCIAS DA SAUDE::FARMACIA
dc.subject.eng.fl_str_mv Semisolids
Nanoparticles
Silymarin
Inflammation
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS DA SAUDE::FARMACIA
description Currently, irritant contact dermatitis is the most prevalent dermatitis among the others and is triggered by the activation of innate immunity after skin contact with irritants. Silibinin (SB), a naturally occurring active, has beneficial activities for the cutaneous tissue, among which the anti-inflammatory action can be highlighted. Thus, in studies conducted in our research group, nanocapsule suspensions containing pomegranate oil as oily core and silibinin as active have been developed. Aiming at the skin application, this dissertation aimed to develop an innovative bioadhesive hydrogel for the delivery of this NC suspension and to verify its potential in the treatment of irritative contact dermatitis. The hydrogel was prepared from the polymer Pemulen® TR2, which has bioadhesive characteristics. The formulations were characterized in terms of SB content, pH, particle size and distribution, as well as spreadability and rheology, important characteristics mainly in the development of new products for dermal administration. For the studies of SB release from the hydrogels and cutaneous permeation of the active in human skin Franz cells were used. The bioadhesiveness test was performed using a texturometer and, in order to guarantee the safety of the formulations, the cutaneous biometry assay was performed, evaluating the parameters of erythema, pH, transepidermal loss of water and skin hydration. Also, considering the ability of SB to regulate inflammatory events, the viability of these hydrogels in the inflammation treatment was studied in an animal model induced by croton oil. The proposed formulations presented physico-chemical characteristics compatible with topical administration, maintaining the nanometric size after incorporation into the hydrogels (184 ± 26 nm), adequate pH range (6.70 ± 0.15), SB concentration close to concentration (0.99 ± 0.01 mg/g), as well as non-Newtonian pseudoplastic behavior. The in vitro release evidenced that the hydrogels containing the nanocapsules provided less silibinin retention in the dosage form for both media: phosphate buffer pH 5.5 plus ethanol and the buffer alone (4.73 ± 0.50 μg / mL for HP-NCSB and 1.14 ± 0.18 μg/mL for HP-SB and 2.25 ± 0.25 μg/mL from HP-NCSB and 0.49 ± 0.05 μg/mL for HP-SB, respectively). Permeation studies on human skin have indicated that the nanoencapsulation of silibinin increases its retention in the stratum corneum, which can act as a deposit for gradual release of this active. Evaluating the bioadhesive potential of the formulations, it was verified that the HP-NCSB stands out against the other formulations tested. In the in vivo study, the hydrogels containing the silibinin nanocapsules and pomegranate oil were able to act by expressively reducing ear edema and inflammatory cells. In the cutaneous biometry test, for all the parameters tested the formulations did not alter the normal skin conditions of the volunteers. Therefore, based on the results obtained, the hydrogel development was successful and the formulation has met the proposed therapeutic purpose, and may be a therapeutic alternative for the treatment of irritant contact dermatitis, using the natural source active silibinin allied to nanotechnology, since it was possible to demonstrate that the hydrogel containing silibinin nanocapsules had satisfactory results against the hydrogel containing non-nanoencapsulated silibinin, as well as it was possible to demonstrate the contribution of Pemulen® TR2 in the performance of the formulations.
publishDate 2018
dc.date.issued.fl_str_mv 2018-11-30
dc.date.accessioned.fl_str_mv 2021-05-25T19:12:55Z
dc.date.available.fl_str_mv 2021-05-25T19:12:55Z
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.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/20985
url http://repositorio.ufsm.br/handle/1/20985
dc.language.iso.fl_str_mv por
language por
dc.relation.cnpq.fl_str_mv 400300000005
dc.relation.confidence.fl_str_mv 600
dc.relation.authority.fl_str_mv 087e54fa-1802-4e8a-a314-a3ffa14190d9
88edf2f5-2ce3-436f-a4b2-2565a2fd22fc
1e373fcc-89bd-4103-adba-676f6dcec787
d4467822-0fe5-4124-912e-ddd78a6dc0fb
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
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 Análises Clínicas e Toxicológicas
publisher.none.fl_str_mv Universidade Federal de Santa Maria
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
bitstream.url.fl_str_mv http://repositorio.ufsm.br/bitstream/1/20985/1/DIS_PPGCF_2018_RIGON_CRISTINA.pdf
http://repositorio.ufsm.br/bitstream/1/20985/2/license_rdf
http://repositorio.ufsm.br/bitstream/1/20985/3/license.txt
http://repositorio.ufsm.br/bitstream/1/20985/4/DIS_PPGCF_2018_RIGON_CRISTINA.pdf.txt
http://repositorio.ufsm.br/bitstream/1/20985/5/DIS_PPGCF_2018_RIGON_CRISTINA.pdf.jpg
bitstream.checksum.fl_str_mv ee2f5d311a17e4827e8702f40a72c60a
4460e5956bc1d1639be9ae6146a50347
2f0571ecee68693bd5cd3f17c1e075df
57282fd1a0fa1ad21e0f4b765f9fcba5
05bff5d43768ccf0ca8648eb2a23231c
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
MD5
MD5
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv
_version_ 1794524385253523456