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In vitro activity of copper(II) complexes, loaded or unloaded into a nanostructured lipid system, against mycobacterium tuberculosis

dc.contributor.authorda Silva, Patricia B. [UNESP]
dc.contributor.authorde Souza, Paula C. [UNESP]
dc.contributor.authorCalixto, Giovana Maria Fioramonti [UNESP]
dc.contributor.authorLopes, Erica de O. [UNESP]
dc.contributor.authorFrem, Regina C. G. [UNESP]
dc.contributor.authorNetto, Adelino V. G. [UNESP]
dc.contributor.authorMauro, Antonio E. [UNESP]
dc.contributor.authorPavan, Fernando R. [UNESP]
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:28:17Z
dc.date.available2018-12-11T17:28:17Z
dc.date.issued2016-05-01
dc.description.abstractTuberculosis (TB) is an infectious disease caused mainly by the bacillus Mycobacterium tuberculosis (Mtb), presenting 9.5 million new cases and 1.5 million deaths in 2014. The aim of this study was to evaluate a nanostructured lipid system (NLS) composed of 10% phase oil (cholesterol), 10% surfactant (soy phosphatidylcholine, sodium oleate), and Eumulgin® HRE 40 ([castor oil polyoxyl-40-hydrogenated] in a proportion of 3:6:8), and an 80% aqueous phase (phosphate buffer pH = 7.4) as a tactic to enhance the in vitro anti-Mtb activity of the copper(II) complexes [CuCl2(INH)2] H2O (1), [Cu(NCS)2(INH)2]5H2O (2) and [Cu(NCO)2(INH)2]4H2O (3). The Cu(II) complex-loaded NLS displayed sizes ranging from 169.5 ± 0.7095 to 211.1 ± 0.8963 nm, polydispersity index (PDI) varying from 0.135 ± 0.0130 to 0.236 ± 0.00100, and zeta potential ranging from -0.00690 ± 0.0896 to 8.43 ± 1.63 mV. Rheological analysis showed that the formulations behave as non-Newtonian fluids of the pseudoplastic and viscoelastic type. Antimycobacterial activities of the free complexes and NLS-loaded complexes against Mtb H37Rv ATCC 27294 were evaluated by the REMA methodology, and the selectivity index (SI) was calculated using the cytotoxicity index (IC50) against Vero (ATCC® CCL-81), J774A.1 (ATCC® TIB-67), and MRC-5 (ATCC® CCL-171) cell lines. The data suggest that the incorporation of the complexes into NLS improved the inhibitory action against Mtb by 52-, 27-, and 4.7-fold and the SI values by 173-, 43-, and 7-fold for the compounds 1, 2 and 3, respectively. The incorporation of the complexes 1, 2 and 3 into the NLS also resulted in a significant decrease of toxicity towards an alternative model (Artemia salina L.). These findings suggest that the NLS may be considered as a platform for incorporation of metallic complexes aimed at the treatment of TB.en
dc.description.affiliationFaculdade de Ciencias Farmaceuticas UNESP—Univ Estadual Paulista, Campus Araraquara
dc.description.affiliationInstituto de Química UNESP—Univ Estadual Paulista, Campus Araraquara
dc.description.affiliationUnespFaculdade de Ciencias Farmaceuticas UNESP—Univ Estadual Paulista, Campus Araraquara
dc.description.affiliationUnespInstituto de Química UNESP—Univ Estadual Paulista, Campus Araraquara
dc.identifierhttp://dx.doi.org/10.3390/ijms17050745
dc.identifier.citationInternational Journal of Molecular Sciences, v. 17, n. 5, 2016.
dc.identifier.doi10.3390/ijms17050745
dc.identifier.file2-s2.0-84968820446.pdf
dc.identifier.issn1422-0067
dc.identifier.issn1661-6596
dc.identifier.lattes7927677053650819
dc.identifier.orcid0000-0002-0057-7964
dc.identifier.scopus2-s2.0-84968820446
dc.identifier.urihttp://hdl.handle.net/11449/178026
dc.language.isoeng
dc.relation.ispartofInternational Journal of Molecular Sciences
dc.relation.ispartofsjr1,260
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectArtemia salina L
dc.subjectCopper(II) complexes
dc.subjectCytotoxicity
dc.subjectMycobacterium tuberculosis
dc.subjectNanostructured lipid system
dc.subjectTuberculosis
dc.titleIn vitro activity of copper(II) complexes, loaded or unloaded into a nanostructured lipid system, against mycobacterium tuberculosisen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublication5004bcab-94af-4939-b980-091ae9d0a19e
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscovery5004bcab-94af-4939-b980-091ae9d0a19e
unesp.author.lattes7927677053650819[6]
unesp.author.lattes3300223970814448[7]
unesp.author.orcid0000-0002-0057-7964[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentCiências Biológicas - FCFpt
unesp.departmentFármacos e Medicamentos - FCFpt
unesp.departmentQuímica Inorgânica - IQARpt

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