Supramolecular cyclodextrin-based metal-organic frameworks as efficient carrier for anti-inflammatory drugs
| dc.contributor.author | Abuçafy, Marina P. [UNESP] | |
| dc.contributor.author | Caetano, Bruno L. [UNESP] | |
| dc.contributor.author | Chiari-Andréo, Bruna G. [UNESP] | |
| dc.contributor.author | Fonseca-Santos, Bruno [UNESP] | |
| dc.contributor.author | do Santos, Aline M. [UNESP] | |
| dc.contributor.author | Chorilli, Marlus [UNESP] | |
| dc.contributor.author | Chiavacci, Leila A. [UNESP] | |
| dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
| dc.date.accessioned | 2018-12-11T17:18:04Z | |
| dc.date.available | 2018-12-11T17:18:04Z | |
| dc.date.issued | 2018-06-01 | |
| dc.description.abstract | Drug 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.affiliation | Department of Drugs and MedicinesSão Paulo State University (UNESP)School of Pharmaceutical Sciences | |
| dc.description.affiliation | Department of Biological and Health SciencesUniversidade de Araraquara – UNIARA | |
| dc.description.affiliationUnesp | Department of Drugs and MedicinesSão Paulo State University (UNESP)School of Pharmaceutical Sciences | |
| dc.format.extent | 112-119 | |
| dc.identifier | http://dx.doi.org/10.1016/j.ejpb.2018.02.009 | |
| dc.identifier.citation | European Journal of Pharmaceutics and Biopharmaceutics, v. 127, p. 112-119. | |
| dc.identifier.doi | 10.1016/j.ejpb.2018.02.009 | |
| dc.identifier.file | 2-s2.0-85042197341.pdf | |
| dc.identifier.issn | 1873-3441 | |
| dc.identifier.issn | 0939-6411 | |
| dc.identifier.lattes | 1427125996716282 | |
| dc.identifier.scopus | 2-s2.0-85042197341 | |
| dc.identifier.uri | http://hdl.handle.net/11449/175903 | |
| dc.language.iso | eng | |
| dc.relation.ispartof | European Journal of Pharmaceutics and Biopharmaceutics | |
| dc.relation.ispartofsjr | 1,342 | |
| dc.rights.accessRights | Acesso aberto | pt |
| dc.source | Scopus | |
| dc.subject | Anti-inflammatory in vivo assay | |
| dc.subject | Drug adsorption | |
| dc.subject | Drug delivery | |
| dc.subject | Metal-organic framework | |
| dc.subject | γ-cyclodextrin | |
| dc.title | Supramolecular cyclodextrin-based metal-organic frameworks as efficient carrier for anti-inflammatory drugs | en |
| dc.type | Artigo | pt |
| dspace.entity.type | Publication | |
| relation.isDepartmentOfPublication | e214da1b-9929-4ae9-b8fd-655e9bfeda4b | |
| relation.isDepartmentOfPublication.latestForDiscovery | e214da1b-9929-4ae9-b8fd-655e9bfeda4b | |
| unesp.author.lattes | 1427125996716282 | |
| unesp.author.orcid | 0000-0001-8247-2092[6] | |
| unesp.department | Fármacos e Medicamentos - FCF | pt |
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