MOF-Based Polymeric Nanocomposite Films as Potential Materials for Drug Delivery Devices in Ocular Therapeutics

Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10045/108755
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dc.contributorMateriales Avanzadoses_ES
dc.contributor.authorGandara-Loe, Jesús-
dc.contributor.authorSouza, Barbara E.-
dc.contributor.authorMissyul, Alexander-
dc.contributor.authorGiraldo, German-
dc.contributor.authorTan, Jin-Chong-
dc.contributor.authorSilvestre-Albero, Joaquín-
dc.contributor.otherUniversidad de Alicante. Departamento de Química Inorgánicaes_ES
dc.contributor.otherUniversidad de Alicante. Instituto Universitario de Materialeses_ES
dc.date.accessioned2020-08-31T15:44:34Z-
dc.date.available2020-08-31T15:44:34Z-
dc.date.issued2020-06-12-
dc.identifier.citationACS Applied Materials & Interfaces. 2020, 12(27): 30189-30197. https://doi.org/10.1021/acsami.0c07517es_ES
dc.identifier.issn1944-8244 (Print)-
dc.identifier.issn1944-8252 (Online)-
dc.identifier.urihttp://hdl.handle.net/10045/108755-
dc.description.abstractNovel MOF-based polymer nanocomposite films were successfully prepared using Zr-based UiO-67 as a metal–organic framework (MOF) and polyurethane (PU) as a polymeric matrix. Synchrotron X-ray powder diffraction (SXRPD) analysis confirms the improved stability of the UiO-67 embedded nanocrystals, and scanning electron microscopy images confirm their homogeneous distribution (average crystal size ∼100–200 nm) within the 50 μm thick film. Accessibility to the inner porous structure of the embedded MOFs was completely suppressed for N2 at cryogenic temperatures. However, ethylene adsorption measurements at 25 °C confirm that at least 45% of the MOF crystals are fully accessible for gas-phase adsorption of nonpolar molecules. Although this partial blockage limits the adsorption performance of the embedded MOFs for ocular drugs (e.g., brimonidine tartrate) compared to the pure MOF, an almost 60-fold improvement in the adsorption capacity was observed for the PU matrix after incorporation of the UiO-67 nanocrystals. The UiO-67@PU nanocomposite exhibits a prolonged release of brimonidine (up to 14 days were quantified). Finally, the combined use of SXRPD, thermogravimetric analysis (TGA), and Fourier transform infrared (FTIR) analyses confirmed the presence of the drug in the nanocomposite film, the stability of the MOF framework and the drug upon loading, and the presence of brimonidine in an amorphous phase once adsorbed. These results open the gate toward the application of these polymeric nanocomposite films for drug delivery in ocular therapeutics, either as a component of a contact lens, in the composition of lacrimal stoppers (e.g., punctal plugs), or in subtenon inserts.es_ES
dc.description.sponsorshipThe authors would like to acknowledge financial support from MINECO (MAT2016-80285-p), Spanish ALBA Synchrotron (Project 2020014008), and H2020 (MSCA-RISE-2016/NanoMed Project). B.E.S. thanks the Minas Gerais Research Foundation (FAPEMIG CNPJ n21.949.888/0001-83) for a DPhil scholarship award. J.-C.T. thanks the EPSRC (Grant No. EP/N014960/1) and ERC Consolidator Grant (PROMOFS under the grant agreement 771575) for funding.es_ES
dc.languageenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.rights© 2020 American Chemical Societyes_ES
dc.subjectBrimonidinees_ES
dc.subjectMOFses_ES
dc.subjectPolyurethanees_ES
dc.subjectOcular plugses_ES
dc.subjectDrug deliveryes_ES
dc.subject.otherQuímica Inorgánicaes_ES
dc.titleMOF-Based Polymeric Nanocomposite Films as Potential Materials for Drug Delivery Devices in Ocular Therapeuticses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.peerreviewedsies_ES
dc.identifier.doi10.1021/acsami.0c07517-
dc.relation.publisherversionhttps://doi.org/10.1021/acsami.0c07517es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/MAT2016-80285-P-
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