Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulations
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1002/adhm.202202720 http://hdl.handle.net/11449/249633 |
Resumo: | Despite their distinctive secondary structure based on cross β-strands, amyloid fibrils (AF) are stable fibrous protein aggregates with features similar to collagen, one of the main components of the extracellular matrix, and thus constitute a potential scaffold for enhancing cell adhesion for topical applications. Here, the contribution of AF to skin bio-adhesivity aiming toward topical treatments is investigated. Liquid crystalline mesophase (LCM) based on phytantriol is formulated, with the aqueous phase containing either water or a solution of 4 wt% amyloid fibrils. Then resveratrol is added as a model anti-inflammatory molecule. The developed LCM presents a double gyroid Ia3d mesophase. The incorporation of AF into the LCM increases its bio-adhesive properties. In vitro release and ex vivo permeation and retention confirm the controlled release property of the system, and that resveratrol is retained in epidermis and dermis, but is also permeated through the skin. All formulations are biocompatible with L929 cells. The in vivo assay confirms that systems with AF lead to a higher anti-inflammatory effect of resveratrol. These results confirm the hypothesis that the incorporation of AF in the LCM increases the bio-adhesiveness and efficiency of the system for topical treatment, and consequently, the therapeutical action of the encapsulated drug. |
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Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulationsamyloid fibrilsbio-adhesivenessinflammatory diseasesliquid crystalline mesophasestopical treatmentsDespite their distinctive secondary structure based on cross β-strands, amyloid fibrils (AF) are stable fibrous protein aggregates with features similar to collagen, one of the main components of the extracellular matrix, and thus constitute a potential scaffold for enhancing cell adhesion for topical applications. Here, the contribution of AF to skin bio-adhesivity aiming toward topical treatments is investigated. Liquid crystalline mesophase (LCM) based on phytantriol is formulated, with the aqueous phase containing either water or a solution of 4 wt% amyloid fibrils. Then resveratrol is added as a model anti-inflammatory molecule. The developed LCM presents a double gyroid Ia3d mesophase. The incorporation of AF into the LCM increases its bio-adhesive properties. In vitro release and ex vivo permeation and retention confirm the controlled release property of the system, and that resveratrol is retained in epidermis and dermis, but is also permeated through the skin. All formulations are biocompatible with L929 cells. The in vivo assay confirms that systems with AF lead to a higher anti-inflammatory effect of resveratrol. These results confirm the hypothesis that the incorporation of AF in the LCM increases the bio-adhesiveness and efficiency of the system for topical treatment, and consequently, the therapeutical action of the encapsulated drug.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Health Sciences & Technology ETH ZurichDepartment of Drugs and Medicine School of Pharmaceutical Sciences São Paulo State University, São PauloPaul Scherrer Institute (PSI)Department of Materials ETH ZurichDepartment of Drugs and Medicine School of Pharmaceutical Sciences São Paulo State University, São PauloFAPESP: 2017/22758-3ETH ZurichUniversidade Estadual Paulista (UNESP)Paul Scherrer Institute (PSI)Victorelli, Francesca DamianiRodero, Camila Fernanda [UNESP]Lutz-Bueno, VivianeChorilli, Marlus [UNESP]Mezzenga, Raffaele2023-07-29T16:04:59Z2023-07-29T16:04:59Z2023-05-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1002/adhm.202202720Advanced Healthcare Materials, v. 12, n. 12, 2023.2192-26592192-2640http://hdl.handle.net/11449/24963310.1002/adhm.2022027202-s2.0-85147411842Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengAdvanced Healthcare Materialsinfo:eu-repo/semantics/openAccess2024-06-24T13:45:29Zoai:repositorio.unesp.br:11449/249633Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-06-24T13:45:29Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulations |
title |
Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulations |
spellingShingle |
Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulations Victorelli, Francesca Damiani amyloid fibrils bio-adhesiveness inflammatory diseases liquid crystalline mesophases topical treatments |
title_short |
Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulations |
title_full |
Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulations |
title_fullStr |
Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulations |
title_full_unstemmed |
Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulations |
title_sort |
Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulations |
author |
Victorelli, Francesca Damiani |
author_facet |
Victorelli, Francesca Damiani Rodero, Camila Fernanda [UNESP] Lutz-Bueno, Viviane Chorilli, Marlus [UNESP] Mezzenga, Raffaele |
author_role |
author |
author2 |
Rodero, Camila Fernanda [UNESP] Lutz-Bueno, Viviane Chorilli, Marlus [UNESP] Mezzenga, Raffaele |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
ETH Zurich Universidade Estadual Paulista (UNESP) Paul Scherrer Institute (PSI) |
dc.contributor.author.fl_str_mv |
Victorelli, Francesca Damiani Rodero, Camila Fernanda [UNESP] Lutz-Bueno, Viviane Chorilli, Marlus [UNESP] Mezzenga, Raffaele |
dc.subject.por.fl_str_mv |
amyloid fibrils bio-adhesiveness inflammatory diseases liquid crystalline mesophases topical treatments |
topic |
amyloid fibrils bio-adhesiveness inflammatory diseases liquid crystalline mesophases topical treatments |
description |
Despite their distinctive secondary structure based on cross β-strands, amyloid fibrils (AF) are stable fibrous protein aggregates with features similar to collagen, one of the main components of the extracellular matrix, and thus constitute a potential scaffold for enhancing cell adhesion for topical applications. Here, the contribution of AF to skin bio-adhesivity aiming toward topical treatments is investigated. Liquid crystalline mesophase (LCM) based on phytantriol is formulated, with the aqueous phase containing either water or a solution of 4 wt% amyloid fibrils. Then resveratrol is added as a model anti-inflammatory molecule. The developed LCM presents a double gyroid Ia3d mesophase. The incorporation of AF into the LCM increases its bio-adhesive properties. In vitro release and ex vivo permeation and retention confirm the controlled release property of the system, and that resveratrol is retained in epidermis and dermis, but is also permeated through the skin. All formulations are biocompatible with L929 cells. The in vivo assay confirms that systems with AF lead to a higher anti-inflammatory effect of resveratrol. These results confirm the hypothesis that the incorporation of AF in the LCM increases the bio-adhesiveness and efficiency of the system for topical treatment, and consequently, the therapeutical action of the encapsulated drug. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-29T16:04:59Z 2023-07-29T16:04:59Z 2023-05-08 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1002/adhm.202202720 Advanced Healthcare Materials, v. 12, n. 12, 2023. 2192-2659 2192-2640 http://hdl.handle.net/11449/249633 10.1002/adhm.202202720 2-s2.0-85147411842 |
url |
http://dx.doi.org/10.1002/adhm.202202720 http://hdl.handle.net/11449/249633 |
identifier_str_mv |
Advanced Healthcare Materials, v. 12, n. 12, 2023. 2192-2659 2192-2640 10.1002/adhm.202202720 2-s2.0-85147411842 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Advanced Healthcare Materials |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1826303778928721920 |