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Copper(II) biocompatible coordination solids as potential platforms for diclofenac delivery systems

dc.contributor.authorAlves, Renata Carolina [UNESP]
dc.contributor.authorLucena, Guilherme Nunes [UNESP]
dc.contributor.authorde Farias, Renan Lira [UNESP]
dc.contributor.authorda Silva, Patrícia Bento [UNESP]
dc.contributor.authorda Silva, Isabel Cristiane [UNESP]
dc.contributor.authorPavan, Fernando Rogério [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.authorda Costa Ferreira, Ana Maria
dc.contributor.authorGalvão Frem, Regina Célia [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2020-12-12T02:11:12Z
dc.date.available2020-12-12T02:11:12Z
dc.date.issued2020-09-01
dc.description.abstractThis study deals a new copper(II)-based cluster-organic framework, CUBA, targeted a matrix for diclofenac sodium delivery. CUBA was prepared by solvothermal reaction and characterized by several techniques. FEG-SEM data revealed presence of random porous over CUBA surface. BET equation fitting N2-adsorption isotherm showed a surface area and pore volume amount to ca. 55 ​m2 ​g-1 and 0.49 ​cm3 ​g-1, respectively. In vitro assays showed non-cytotoxic activity for CUBA in MRC-5 ​cell line. A microporous copper(II)-based metal-organic framework, herein labelled as BioMOF-Cu, was used as a comparison in drug load-releasing tests. CUBA exhibited encapsulation efficiency of 29.47, 36.74 and 60.72% at 2, 4 and 7 days, respectively, BioMOF-Cu showed 84.68% at 4 days. In PBS solution CUBA ranged at 13-18% of total drug-releasing at 72 ​h and BioMOF-Cu afforded 21% at 48 ​h. In vivo evaluation of the anti-inflammatory effects, CUBA and BioMOF-Cu decreased the paw edema when compared to the negative group.en
dc.description.affiliationSão Paulo State University (UNESP) Institute of Chemistry
dc.description.affiliationSão Paulo State University (UNESP) School of Pharmaceutical Sciences Department of Drugs and Medicines
dc.description.affiliationSão Paulo State University (UNESP) School of Pharmaceutical Sciences Department of Biological Sciences
dc.description.affiliationUniversity of São Paulo (USP) Institute of Chemistry Department of Fundamental Chemistry
dc.description.affiliationUnespSão Paulo State University (UNESP) Institute of Chemistry
dc.description.affiliationUnespSão Paulo State University (UNESP) School of Pharmaceutical Sciences Department of Drugs and Medicines
dc.description.affiliationUnespSão Paulo State University (UNESP) School of Pharmaceutical Sciences Department of Biological Sciences
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipIdCAPES: 001
dc.identifierhttp://dx.doi.org/10.1016/j.jssc.2020.121479
dc.identifier.citationJournal of Solid State Chemistry, v. 289.
dc.identifier.doi10.1016/j.jssc.2020.121479
dc.identifier.issn1095-726X
dc.identifier.issn0022-4596
dc.identifier.scopus2-s2.0-85086478408
dc.identifier.urihttp://hdl.handle.net/11449/200609
dc.language.isoeng
dc.relation.ispartofJournal of Solid State Chemistry
dc.sourceScopus
dc.subjectCluster-organic framework
dc.subjectDiclofenac sodium
dc.subjectDrug delivery
dc.subjectIn vivo evaluation
dc.titleCopper(II) biocompatible coordination solids as potential platforms for diclofenac delivery systemsen
dc.typeArtigo
unesp.departmentCiências Biológicas - FCFpt
unesp.departmentFármacos e Medicamentos - FCFpt

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