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Supramolecular cyclodextrin-based metal-organic frameworks as efficient carrier for anti-inflammatory drugs

dc.contributor.authorAbuçafy, Marina P. [UNESP]
dc.contributor.authorCaetano, Bruno L. [UNESP]
dc.contributor.authorChiari-Andréo, Bruna G. [UNESP]
dc.contributor.authorFonseca-Santos, Bruno [UNESP]
dc.contributor.authordo Santos, Aline M. [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.authorChiavacci, Leila A. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:18:04Z
dc.date.available2018-12-11T17:18:04Z
dc.date.issued2018-06-01
dc.description.abstractDrug delivery systems have been used to reduce adverse effects and improve the efficacy of therapies. Drug carriers have been developed over the years, but they have limitations. γ-cyclodextrin-based metal-organic frameworks (γ-CD-MOF) have significant advantages due to their biocompatibility and environmental safety, besides crystallinity and porosity. Herein, γ-CD-MOFs were synthesised with different metals as nodes and investigated. Uniform mesoporous γ-CD-MOFs were obtained and showed an absence of toxicity in HepG2 and Caco-2 cells. The longer controlled release was verified for γ-CD-MOFs, with a maximum of 62% released in 12 h. An inflammation experiment was performed in mice and activity equivalent to the positive control was verified. γ-KCD-MOFs and γ-NaCD-MOFs reached activity after 6 h of administration, however this happened after 24 h in γ-FeCD-MOFs, being more effective than the positive control. Considering the ability for drug entrapment, easy preparation and controlled release, this class of material allows potential applications in drug delivery systems.en
dc.description.affiliationDepartment of Drugs and MedicinesSão Paulo State University (UNESP)School of Pharmaceutical Sciences
dc.description.affiliationDepartment of Biological and Health SciencesUniversidade de Araraquara – UNIARA
dc.description.affiliationUnespDepartment of Drugs and MedicinesSão Paulo State University (UNESP)School of Pharmaceutical Sciences
dc.format.extent112-119
dc.identifierhttp://dx.doi.org/10.1016/j.ejpb.2018.02.009
dc.identifier.citationEuropean Journal of Pharmaceutics and Biopharmaceutics, v. 127, p. 112-119.
dc.identifier.doi10.1016/j.ejpb.2018.02.009
dc.identifier.file2-s2.0-85042197341.pdf
dc.identifier.issn1873-3441
dc.identifier.issn0939-6411
dc.identifier.lattes1427125996716282
dc.identifier.scopus2-s2.0-85042197341
dc.identifier.urihttp://hdl.handle.net/11449/175903
dc.language.isoeng
dc.relation.ispartofEuropean Journal of Pharmaceutics and Biopharmaceutics
dc.relation.ispartofsjr1,342
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectAnti-inflammatory in vivo assay
dc.subjectDrug adsorption
dc.subjectDrug delivery
dc.subjectMetal-organic framework
dc.subjectγ-cyclodextrin
dc.titleSupramolecular cyclodextrin-based metal-organic frameworks as efficient carrier for anti-inflammatory drugsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
unesp.author.lattes1427125996716282
unesp.author.orcid0000-0001-8247-2092[6]
unesp.departmentFármacos e Medicamentos - FCFpt

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