Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/19769
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dc.contributor.authorFigueiredo, Andrea G. P. R.pt
dc.contributor.authorFigueiredo, Ana R. P.pt
dc.contributor.authorAlonso-Varona, Anapt
dc.contributor.authorFernandes, Susana C. M.pt
dc.contributor.authorPalomares, Teodoropt
dc.contributor.authorRubio-Azpeitia, Evapt
dc.contributor.authorBarros-Timmons, Anapt
dc.contributor.authorSilvestre, Armando J. D.pt
dc.contributor.authorNeto, Carlos Pascoalpt
dc.contributor.authorFreire, Carmen S. R.pt
dc.date.accessioned2017-12-07T19:24:13Z-
dc.date.available2017-12-07T19:24:13Z-
dc.date.issued2013pt
dc.identifier.issn2314-6133pt
dc.identifier.urihttp://hdl.handle.net/10773/19769-
dc.description.abstractA series of bacterial cellulose-poly(2-hydroxyethyl methacrylate) nanocomposite films was prepared by in situ radical polymerization of 2-hydroxyethyl methacrylate (HEMA), using variable amounts of poly(ethylene glycol) diacrylate (PEGDA) as crosslinker. Thin films were obtained, and their physical, chemical, thermal, and mechanical properties were evaluated. The films showed improved translucency compared to BC and enhanced thermal stability and mechanical performance when compared to poly(2-hydroxyethyl methacrylate) (PHEMA). Finally, BC/PHEMA nanocomposites proved to be nontoxic to human adipose-derived mesenchymal stem cells (ADSCs) and thus are pointed as potential dry dressings for biomedical applications.pt
dc.language.isoengpt
dc.publisherHINDAWI PUBLISHING CORPORATIONpt
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F63219%2F2009/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F70119%2F2010/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/COMPETE/132936/PTpt
dc.rightsopenAccesspor
dc.subjectCELLULOSEpt
dc.subjectHYDROGELSpt
dc.subjectCOMPOSITESpt
dc.subjectSCAFFOLDSpt
dc.subjectDIFFUSIONpt
dc.subjectDELIVERYpt
dc.subjectPHEMApt
dc.titleBiocompatible Bacterial Cellulose-Poly(2-hydroxyethyl methacrylate) Nanocomposite Filmspt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.titleBIOMED RESEARCH INTERNATIONALpt
dc.relation.publisherversion10.1155/2013/698141pt
dc.identifier.doi10.1155/2013/698141pt
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