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dc.contributor.authorCosta, Rui R.
dc.contributor.authorGirotti, Alessandra
dc.contributor.authorSantos, Mercedes
dc.contributor.authorArias, F. Javier
dc.contributor.authorMano, João F.
dc.contributor.authorRodríguez-Cabello, J. Carlos
dc.date.accessioned2026-02-17T10:29:01Z
dc.date.available2026-02-17T10:29:01Z
dc.date.issued2014
dc.identifier.citationActa Biomaterialia Volume 10, Issue 6, June 2014, Pages 2653-2662es
dc.identifier.issn1742-7061es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/82818
dc.description.abstractMultilayered microcapsules of chitosan and biomimetic elastin-like recombinamers (ELRs) were prepared envisaging the intracellular delivery of active agents. Two ELRs containing either a bioactive RGD sequence or a scrambled non-functional RDG were used to construct two types of functionalized polymeric microcapsules, both of spherical shape ∼4 μm in diameter. Cell viability studies with human mesenchymal stem cells (hMSCs) were performed using microcapsule/cell ratios between 5:1 and 100:1. After 3 and 72 h of co-incubation, no signs of cytotoxicity were found, but cells incubated with RGD-functionalized microcapsules exhibited higher viability values than RDG cells. The internalization efficacy and bioavailability of encapsulated DQ-ovalbumin were assessed by monitoring the fluorescence changes in the cargo. The data show that surface functionalization did not significantly influence internalization by hMSCs, but the bioavailability of DQ-ovalbumin degraded faster when encapsulated within RGD-functionalized microcapsules. The microcapsules developed show promise for intracellular drug delivery with increased drug efficacy.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherElsevieres
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.titleCellular uptake of multilayered capsules produced with natural and genetically engineered biomimetic macromoleculeses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1016/j.actbio.2014.02.020es
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S1742706114000725?via%3Dihub#ak005es
dc.identifier.publicationfirstpage2653es
dc.identifier.publicationissue6es
dc.identifier.publicationlastpage2662es
dc.identifier.publicationtitleActa Biomaterialiaes
dc.identifier.publicationvolume10es
dc.peerreviewedSIes
dc.description.projectThe authors acknowledge financial support from Fundação para a Ciência e Tecnologia (Grant SFRH/BD/61126/2009), “Fundo Social Europeu”, “Programa Diferencial de Potencial Humano”, EU 7th Framework Programme (No. REGPOT-CT2012-316331-POLARIS), the EU through the European Regional Development Fund (ERDF), from the MINECO (MAT-2010-15982, MAT2010-15310, PRI-PIBAR-2011-1403 and MAT2012-38043), the JCyL (projects VA049A11, VA152A12 and VA155A12), the CIBER-BBN, and the Instituto de Salud Carlos III under the “Network Center of Regenerative Medicine and Cellular Therapy of Castilla and Leon”.es
dc.type.hasVersioninfo:eu-repo/semantics/submittedVersiones


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