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Publicação:
Highly Controlled Diffusion Drug Release from Ureasil-Poly(ethylene oxide)-Na+-Montmorillonite Hybrid Hydrogel Nanocomposites

dc.contributor.authorJesus, Celso R.N. [UNESP]
dc.contributor.authorMolina, Eduardo F.
dc.contributor.authorPulcinelli, Sandra H. [UNESP]
dc.contributor.authorSantilli, Celso V. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de Franca
dc.date.accessioned2018-12-11T17:37:06Z
dc.date.available2018-12-11T17:37:06Z
dc.date.issued2018-06-06
dc.description.abstractIn this work, we report the effects of incorporation of variable amounts (1-20 wt %) of sodium montmorillonite (MMT) into a siloxane-poly(ethylene oxide) hybrid hydrogel prepared by the sol-gel route. The aim was to control the nanostructural features of the nanocomposite, improve the release profile of the sodium diclofenac (SDCF) drug, and optimize the swelling behavior of the hydrophilic matrix. The nanoscopic characteristics of the siloxane-cross-linked poly(ethylene oxide) network, the semicrystallinity of the hybrid, and the intercalated or exfoliated structure of the clay were investigated by X-ray diffraction, small-angle X-ray scattering, and differential scanning calorimetry. The correlation between the nanoscopic features of nanocomposites containing different amounts of MMT and the swelling behavior revealed the key role of exfoliated silicate in controlling the water uptake by means of a flow barrier effect. The release of the drug from the nanocomposite displayed a stepped pattern kinetically controlled by the diffusion of SDCF molecules through the mass transport barrier created by the exfoliated silicate. The sustained SDCF release provided by the hybrid hydrogel nanocomposite could be useful for the prolonged treatment of painful conditions, such as arthritis, sprains and strains, gout, migraine, and pain after surgical procedures.en
dc.description.affiliationInstituto de Química UNESP, Rua Professor Francisco Degni 55
dc.description.affiliationUniversidade de Franca, Av. Dr. Armando Salles Oliveira 201
dc.description.affiliationUnespInstituto de Química UNESP, Rua Professor Francisco Degni 55
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdCNPq: 304900/2011-7
dc.description.sponsorshipIdCAPES: INCT465593/2014-3
dc.description.sponsorshipIdFAPESP: INCT465593/2014-3
dc.format.extent19059-19068
dc.identifierhttp://dx.doi.org/10.1021/acsami.8b04559
dc.identifier.citationACS Applied Materials and Interfaces, v. 10, n. 22, p. 19059-19068, 2018.
dc.identifier.doi10.1021/acsami.8b04559
dc.identifier.issn1944-8252
dc.identifier.issn1944-8244
dc.identifier.lattes5584298681870865
dc.identifier.orcid0000-0002-8356-8093
dc.identifier.scopus2-s2.0-85047097157
dc.identifier.urihttp://hdl.handle.net/11449/179870
dc.language.isoeng
dc.relation.ispartofACS Applied Materials and Interfaces
dc.relation.ispartofsjr2,784
dc.relation.ispartofsjr2,784
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectdrug delivery
dc.subjectmontmorillonite
dc.subjectnanocomposite
dc.subjectsiloxane-polyether
dc.subjectswelling
dc.titleHighly Controlled Diffusion Drug Release from Ureasil-Poly(ethylene oxide)-Na+-Montmorillonite Hybrid Hydrogel Nanocompositesen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes5584298681870865[4]
unesp.author.orcid0000-0002-3574-2923[2]
unesp.author.orcid0000-0002-8356-8093[4]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentFísico-Química - IQARpt

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