Please use this identifier to cite or link to this item: https://dipositint.ub.edu/dspace/handle/2445/201873
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dc.contributor.authorRaptopoulos, Michail-
dc.contributor.authorFischer, Nicholas G.-
dc.contributor.authorAparicio, Conrado-
dc.date.accessioned2023-09-13T10:45:07Z-
dc.date.available2023-09-13T10:45:07Z-
dc.date.issued2023-01-09-
dc.identifier.issn1097-4636-
dc.identifier.urihttps://hdl.handle.net/2445/201873-
dc.description.abstractPrevious studies have shown hydrophilic/hydrophobic implant surfaces stimulate/hinder osseointegration. An analogous concept was applied here using common biological functional groups on a model surface to promote oral keratinocytes (OKs) proliferation and hemidesmosomes (HD) to extend implant lifespans through increased soft tissue attachment. However, it is unclear what physicochemistry stimulates HDs. Thus, common biological functional groups (NH2 , OH, and CH3 ) were functionalized on glass using silanization. Non-functionalized plasma-cleaned glass and H silanization were controls. Surface modifications were confirmed with X-ray photoelectron spectroscopy and water contact angle. The amount of bovine serum albumin (BSA) and fibrinogen, and BSA thickness, were assessed to understand how adsorbed protein properties were influenced by physicochemistry and may influence HDs. OKs proliferation was measured, and HDs were quantified with immunofluorescence for collagen XVII and integrin β4. Plasma-cleaned surfaces were the most hydrophilic group overall, while CH3 was the most hydrophobic and OH was the most hydrophilic among functionalized groups. Modification with the OH chemical group showed the highest OKs proliferation and HD expression. The OKs response on OH surfaces appeared to not correlate to the amount or thickness of adsorbed model proteins. These results reveal relevant surface physicochemical features to favor HDs and improve implant soft tissue attachment.© 2023 The Authors. Journal of Biomedical Materials Research Part A published by Wiley Periodicals LLC.-
dc.format.extent10 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherWiley-
dc.relation.isformatofhttps://doi.org/10.1002/jbm.a.37486-
dc.relation.ispartofJournal Of Biomedical Materials Research Part a, 2023, vol. 111, num. 7, p. 1021-1030-
dc.relation.urihttps://doi.org/10.1002/jbm.a.37486-
dc.rightscc by-nc-nd (c) Raptopoulos, Michail et al., 2023-
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.sourceArticles publicats en revistes (Institut de Bioenginyeria de Catalunya (IBEC))-
dc.subject.classificationImplants artificials-
dc.subject.classificationRebuig (Biologia)-
dc.subject.classificationQuímica física-
dc.subject.otherArtificial implants-
dc.subject.otherGraft rejection-
dc.subject.otherPhysical and theoretical chemistry-
dc.titleImplant surface physicochemistry affects keratinocyte hemidesmosome formation-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2023-09-06T09:16:37Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.idimarina6573892-
dc.identifier.pmid36621832-
Appears in Collections:Articles publicats en revistes (Institut de Bioenginyeria de Catalunya (IBEC))

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