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dc.contributor.author
Victorelli, Francesca Damiani
dc.contributor.author
Rodero, Camila Fernanda
dc.contributor.author
Lutz Bueno, Viviane
dc.contributor.author
Chorilli, Marlus
dc.contributor.author
Mezzenga, Raffaele
dc.date.accessioned
2023-05-09T14:37:55Z
dc.date.available
2023-02-20T07:28:09Z
dc.date.available
2023-02-20T11:11:40Z
dc.date.available
2023-05-09T14:37:55Z
dc.date.issued
2023-05-08
dc.identifier.issn
2192-2640
dc.identifier.issn
2192-2659
dc.identifier.other
10.1002/adhm.202202720
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/599439
dc.identifier.doi
10.3929/ethz-b-000599439
dc.description.abstract
Despite their distinctive secondary structure based on cross beta-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.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
Wiley-VCH
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
amyloid fibrils
en_US
dc.subject
bio-adhesiveness
en_US
dc.subject
inflammatory diseases
en_US
dc.subject
liquid crystalline mesophases
en_US
dc.subject
topical treatments
en_US
dc.title
Amyloid Fibrils Enhance the Topical Bio-Adhesivity of Liquid Crystalline Mesophase-Based Drug Formulations
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
dc.date.published
2023-01-21
ethz.journal.title
Advanced Healthcare Materials
ethz.journal.volume
12
en_US
ethz.journal.issue
12
en_US
ethz.journal.abbreviated
Adv. Healthcare Mater.
ethz.pages.start
2202720
en_US
ethz.size
9 p.
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
Weinheim
en_US
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02070 - Dep. Gesundheitswiss. und Technologie / Dep. of Health Sciences and Technology::02701 - Inst.f. Lebensmittelwiss.,Ernährung,Ges. / Institute of Food, Nutrition, and Health::03857 - Mezzenga, Raffaele / Mezzenga, Raffaele
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02070 - Dep. Gesundheitswiss. und Technologie / Dep. of Health Sciences and Technology::02701 - Inst.f. Lebensmittelwiss.,Ernährung,Ges. / Institute of Food, Nutrition, and Health::03857 - Mezzenga, Raffaele / Mezzenga, Raffaele
ethz.date.deposited
2023-02-20T07:28:10Z
ethz.source
WOS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2024-02-02T23:00:53Z
ethz.rosetta.lastUpdated
2024-02-02T23:00:53Z
ethz.rosetta.versionExported
true
ethz.COinS
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