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Bionanocomposites based on mesoporous silica and alginate for enhanced drug delivery

dc.contributor.authorde Lima, Hugo H.C.
dc.contributor.authorKupfer, Vicente L.
dc.contributor.authorMoisés, Murilo P.
dc.contributor.authorGuilherme, Marcos R.
dc.contributor.authorde C. Rinaldi, Jaqueline [UNESP]
dc.contributor.authorFelisbino, Sérgio L. [UNESP]
dc.contributor.authorRubira, Adley F.
dc.contributor.authorRinaldi, Andrelson W.
dc.contributor.institutionUniversidade Estadual de Maringá (UEM)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionFederal University of Technology of Paraná-UTFPR
dc.date.accessioned2018-12-11T16:53:18Z
dc.date.available2018-12-11T16:53:18Z
dc.date.issued2018-09-15
dc.description.abstractThis work reports the preparation, the characterization and the prednisolone release profile of biocompatible hydrogel nanocomposites containing mesoporous silica (SBA) and alginate as a biomaterial for enhanced drug delivery with reduced burst effect and improved mechanical properties. Such systems, which were prepared using specific SBA/alginate-crosslinking chemistry, exhibited interconnecting pore hybrid network owing to both mesoporous silica and hydrogel characteristics. Activated SBA was shown to be a determinant factor in inhibiting initial burst by nearly 90% and the drug was released with minimal burst kinetics. The nanoparticles reduced the movements of polymer chains, affecting macromolecular relaxation, and the distribution of mesoporous silica within the hydrogel made drug release into surrounding liquid less favorable. The proposed systems are biocompatible with human immortalized RWPE-1 prostatic epithelial cells. This report offers an approach of up-to-date interest for the development of advanced biomaterials for further physiological and pathological applications.en
dc.description.affiliationMaterials Chemistry and Sensors Laboratory – LMSen State University of Maringá – UEM, 5790 Colombo Avenue
dc.description.affiliationState University of Maringá UEM, 5790 Colombo Avenue
dc.description.affiliationLaboratory of Extracelular Matrix – LabMec São Paulo State University – UNESP
dc.description.affiliationFederal University of Technology of Paraná-UTFPR, 635 Marcílio Dias Street
dc.description.affiliationUnespLaboratory of Extracelular Matrix – LabMec São Paulo State University – UNESP
dc.format.extent126-134
dc.identifierhttp://dx.doi.org/10.1016/j.carbpol.2018.04.107
dc.identifier.citationCarbohydrate Polymers, v. 196, p. 126-134.
dc.identifier.doi10.1016/j.carbpol.2018.04.107
dc.identifier.file2-s2.0-85047068664.pdf
dc.identifier.issn0144-8617
dc.identifier.scopus2-s2.0-85047068664
dc.identifier.urihttp://hdl.handle.net/11449/170999
dc.language.isoeng
dc.relation.ispartofCarbohydrate Polymers
dc.relation.ispartofsjr1,428
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectBiomaterials
dc.subjectCytotoxicity
dc.subjectDrug delivery
dc.subjectHydrogel
dc.subjectMesoporous silica
dc.subjectNanotechnology
dc.titleBionanocomposites based on mesoporous silica and alginate for enhanced drug deliveryen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0003-1202-0896[1]

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