Copper(II) biocompatible coordination solids as potential platforms for diclofenac delivery systems
dc.contributor.author | Alves, Renata Carolina [UNESP] | |
dc.contributor.author | Lucena, Guilherme Nunes [UNESP] | |
dc.contributor.author | de Farias, Renan Lira [UNESP] | |
dc.contributor.author | da Silva, Patrícia Bento [UNESP] | |
dc.contributor.author | da Silva, Isabel Cristiane [UNESP] | |
dc.contributor.author | Pavan, Fernando Rogério [UNESP] | |
dc.contributor.author | Chorilli, Marlus [UNESP] | |
dc.contributor.author | da Costa Ferreira, Ana Maria | |
dc.contributor.author | Galvão Frem, Regina Célia [UNESP] | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.contributor.institution | Universidade de São Paulo (USP) | |
dc.date.accessioned | 2020-12-12T02:11:12Z | |
dc.date.available | 2020-12-12T02:11:12Z | |
dc.date.issued | 2020-09-01 | |
dc.description.abstract | This 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.affiliation | São Paulo State University (UNESP) Institute of Chemistry | |
dc.description.affiliation | São Paulo State University (UNESP) School of Pharmaceutical Sciences Department of Drugs and Medicines | |
dc.description.affiliation | São Paulo State University (UNESP) School of Pharmaceutical Sciences Department of Biological Sciences | |
dc.description.affiliation | University of São Paulo (USP) Institute of Chemistry Department of Fundamental Chemistry | |
dc.description.affiliationUnesp | São Paulo State University (UNESP) Institute of Chemistry | |
dc.description.affiliationUnesp | São Paulo State University (UNESP) School of Pharmaceutical Sciences Department of Drugs and Medicines | |
dc.description.affiliationUnesp | São Paulo State University (UNESP) School of Pharmaceutical Sciences Department of Biological Sciences | |
dc.description.sponsorship | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description.sponsorship | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) | |
dc.description.sponsorshipId | CAPES: 001 | |
dc.identifier | http://dx.doi.org/10.1016/j.jssc.2020.121479 | |
dc.identifier.citation | Journal of Solid State Chemistry, v. 289. | |
dc.identifier.doi | 10.1016/j.jssc.2020.121479 | |
dc.identifier.issn | 1095-726X | |
dc.identifier.issn | 0022-4596 | |
dc.identifier.scopus | 2-s2.0-85086478408 | |
dc.identifier.uri | http://hdl.handle.net/11449/200609 | |
dc.language.iso | eng | |
dc.relation.ispartof | Journal of Solid State Chemistry | |
dc.source | Scopus | |
dc.subject | Cluster-organic framework | |
dc.subject | Diclofenac sodium | |
dc.subject | Drug delivery | |
dc.subject | In vivo evaluation | |
dc.title | Copper(II) biocompatible coordination solids as potential platforms for diclofenac delivery systems | en |
dc.type | Artigo | |
unesp.department | Ciências Biológicas - FCF | pt |
unesp.department | Fármacos e Medicamentos - FCF | pt |