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Synthesis and evaluation of the potential deleterious effects of ZnO nanomaterials (nanoneedles and nanoflowers) on blood components, including albumin, erythrocytes and human isolated primary neutrophils

dc.contributor.authorPastrello, Bruna [UNESP]
dc.contributor.authorParacatu, Luana Chiquetto [UNESP]
dc.contributor.authorde Carvalho Bertozo, Luiza [UNESP]
dc.contributor.authorPaino, Iêda Maria Martinez
dc.contributor.authorLisboa-Filho, Paulo Noronha [UNESP]
dc.contributor.authorXimenes, Valdecir Farias [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2018-12-11T17:04:50Z
dc.date.available2018-12-11T17:04:50Z
dc.date.issued2016-06-01
dc.description.abstractThe application of zinc oxide (ZnO) nanoparticles in biomaterials has increased significantly in the recent years. Here, we aimed to study the potential deleterious effects of ZnO on blood components, including human serum albumin (HSA), erythrocytes and human isolated primary neutrophils. To test the influence of the morphology of the nanomaterials, ZnO nanoneedles (ZnO-nn) and nanoflowers (ZnO-nf) were synthesized. The zeta potential and mean size of ZnO-nf and ZnO-nn suspensions in phosphate-buffered saline were −10.73 mV and 3.81 nm and −5.27 mV and 18.26 nm, respectively. The incubation of ZnO with HSA did not cause its denaturation as verified by the absence of significant alterations in the intrinsic and extrinsic fluorescence and in the circular dichroism spectrum of the protein. The capacity of HSA as a drug carrier was not affected as verified by employing site I and II fluorescent markers. Neither type of ZnO was able to provoke the activation of neutrophils, as verified by lucigenin- and luminol-dependent chemiluminescence and by the extracellular release of hydrogen peroxide. ZnO-nf, but not ZnO-nn, induced the haemolysis of erythrocytes. In conclusion, our results reinforce the concept that ZnO nanomaterials are relatively safe for usage in biomaterials. A potential exception is the capacity of ZnO-nf to promote the lysis of erythrocytes, a discovery that shows the importance of the morphology in the toxicity of nanoparticles.en
dc.description.affiliationDepartment of Chemistry Faculty of Sciences São Paulo State University (UNESP), P.O. Box 473
dc.description.affiliationDepartment of Clinical Analysis School of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.description.affiliationNanomedicine and Nanotoxicology Group Physics Institute of São Carlos (IFSC) University of São Paulo (USP)
dc.description.affiliationDepartment of Physics Faculty of Sciences São Paulo State University (UNESP)
dc.description.affiliationUnespDepartment of Chemistry Faculty of Sciences São Paulo State University (UNESP), P.O. Box 473
dc.description.affiliationUnespDepartment of Clinical Analysis School of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.description.affiliationUnespDepartment of Physics Faculty of Sciences São Paulo State University (UNESP)
dc.identifierhttp://dx.doi.org/10.1007/s11051-016-3527-6
dc.identifier.citationJournal of Nanoparticle Research, v. 18, n. 7, 2016.
dc.identifier.doi10.1007/s11051-016-3527-6
dc.identifier.file2-s2.0-84982693929.pdf
dc.identifier.issn1572-896X
dc.identifier.issn1388-0764
dc.identifier.lattes1353862414532005
dc.identifier.orcid0000-0002-7734-4069
dc.identifier.scopus2-s2.0-84982693929
dc.identifier.urihttp://hdl.handle.net/11449/173364
dc.language.isoeng
dc.relation.ispartofJournal of Nanoparticle Research
dc.relation.ispartofsjr0,528
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectErythrocytes
dc.subjectHealth effects
dc.subjectHuman serum albumin
dc.subjectMetal oxide nanoparticles
dc.subjectNeutrophils
dc.subjectSonochemistry
dc.subjectZinc oxide nanoparticles
dc.titleSynthesis and evaluation of the potential deleterious effects of ZnO nanomaterials (nanoneedles and nanoflowers) on blood components, including albumin, erythrocytes and human isolated primary neutrophilsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
unesp.author.lattes1353862414532005[5]
unesp.author.orcid0000-0002-7734-4069[5]
unesp.departmentAnálises Clínicas - FCFpt

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