| dc.contributor.author | Costa, Rui R. | |
| dc.contributor.author | Girotti, Alessandra | |
| dc.contributor.author | Santos, Mercedes | |
| dc.contributor.author | Arias, F. Javier | |
| dc.contributor.author | Mano, João F. | |
| dc.contributor.author | Rodríguez-Cabello, J. Carlos | |
| dc.date.accessioned | 2026-02-17T10:29:01Z | |
| dc.date.available | 2026-02-17T10:29:01Z | |
| dc.date.issued | 2014 | |
| dc.identifier.citation | Acta Biomaterialia Volume 10, Issue 6, June 2014, Pages 2653-2662 | es |
| dc.identifier.issn | 1742-7061 | es |
| dc.identifier.uri | https://uvadoc.uva.es/handle/10324/82818 | |
| dc.description.abstract | Multilayered 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.mimetype | application/pdf | es |
| dc.language.iso | eng | es |
| dc.publisher | Elsevier | es |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | es |
| dc.title | Cellular uptake of multilayered capsules produced with natural and genetically engineered biomimetic macromolecules | es |
| dc.type | info:eu-repo/semantics/article | es |
| dc.identifier.doi | 10.1016/j.actbio.2014.02.020 | es |
| dc.relation.publisherversion | https://www.sciencedirect.com/science/article/pii/S1742706114000725?via%3Dihub#ak005 | es |
| dc.identifier.publicationfirstpage | 2653 | es |
| dc.identifier.publicationissue | 6 | es |
| dc.identifier.publicationlastpage | 2662 | es |
| dc.identifier.publicationtitle | Acta Biomaterialia | es |
| dc.identifier.publicationvolume | 10 | es |
| dc.peerreviewed | SI | es |
| dc.description.project | The 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.hasVersion | info:eu-repo/semantics/submittedVersion | es |