Gas-Phase Fluorination on PLA Improves Cell Adhesion and Spreading

dc.bibliographicCitation.firstPage5498eng
dc.bibliographicCitation.issue10eng
dc.bibliographicCitation.lastPage5507eng
dc.bibliographicCitation.volume5eng
dc.contributor.authorSchroepfer, Michaela
dc.contributor.authorJunghans, Frauke
dc.contributor.authorVoigt, Diana
dc.contributor.authorMeyer, Michael
dc.contributor.authorBreier, Anette
dc.contributor.authorSchulze-Tanzil, Gundula
dc.contributor.authorPrade, Ina
dc.date.accessioned2021-09-07T11:29:59Z
dc.date.available2021-09-07T11:29:59Z
dc.date.issued2020
dc.description.abstractFor the regeneration or creation of functional tissues, biodegradable biomaterials including polylactic acid (PLA) are widely preferred. Modifications of the material surface are quite common to improve cell-material interactions and thereby support the biological outcome. Typical approaches include a wet chemical treatment with mostly hazardous substances or a functionalization with plasma. In the present study, gas-phase fluorination was applied to functionalize the PLA surfaces in a simple and one-step process. The biological response including biocompatibility, cell adhesion, cell spreading, and proliferation was analyzed in cell culture experiments with fibroblasts L929 and correlated with changes in the surface properties. Surface characterization methods including surface energy and isoelectric point measurements, X-ray photoelectron spectroscopy, and atomic force microscopy were applied to identify the effects of fluorination on PLA. Gas-phase fluorination causes the formation of C-F bonds in the PLA backbone, which induce a shift to a more hydrophilic and polar surface. The slightly negatively charged surface dramatically improves cell adhesion and spreading of cells on the PLA even with low fluorine content. The results indicate that this improved biological response is protein-but not integrin-dependent. Gas-phase fluorination is therefore an efficient technique to improve cellular response to biomaterial surfaces without losing cytocompatibility. Copyright © 2020 American Chemical Society.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/6731
dc.identifier.urihttps://doi.org/10.34657/5778
dc.language.isoengeng
dc.publisherWashington, DC : Soc.eng
dc.relation.doihttps://doi.org/10.1021/acsomega.0c00126
dc.relation.essn1944-8252
dc.relation.ispartofseriesACS applied materials & interfaces 5 (2020), Nr. 10eng
dc.relation.issn1944-8244
dc.rights.licenseACS AuthorChoiceeng
dc.rights.urihttps://pubs.acs.org/page/policy/authorchoice_termsofuse.htmleng
dc.subjectPlasticseng
dc.subjectOrganic polymerseng
dc.subjectCell physiologyeng
dc.subjectFluorineeng
dc.subjectBiopolymersger
dc.subject.ddc540eng
dc.subject.ddc600eng
dc.titleGas-Phase Fluorination on PLA Improves Cell Adhesion and Spreadingeng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleACS applied materials & interfaceseng
tib.accessRightsopenAccesseng
wgl.contributorIPFeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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