Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulations

Detalhes bibliográficos
Autor(a) principal: Victorelli, Francesca Damiani
Data de Publicação: 2023
Outros Autores: Rodero, Camila Fernanda [UNESP], Lutz-Bueno, Viviane, Chorilli, Marlus [UNESP], Mezzenga, Raffaele
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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spelling 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/requestopendoar: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
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