Cytotoxic Effects Caused by Functionalized Carbon Nanotube in Murine Macrophages
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Otros documentos de la autoría: Godoy, Krissia; rodolpho, joice; Dias de Lima Fragelli, Bruna; Camillo, Luciana; Brassolatti, Patricia; Assis, Marcelo de; Nogueira, Camila; Speglich, Carlos; Longo, Elson; Anibal, Fernanda de Freitas
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Mostrar el registro completo del ítemcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7013
comunitat-uji-handle3:10234/8638
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Título
Cytotoxic Effects Caused by Functionalized Carbon Nanotube in Murine MacrophagesAutoría
Fecha de publicación
2022-09-28Editor
Cell Physiol Biochem PressCita bibliográfica
FRANCO DE GODOY, Krissia, et al. Cytotoxic Effects Caused by Functionalized Carbon Nanotube in Murine Macrophages. Cell Physiol Biochem, 2022, vol. 56, p. 514-529.Tipo de documento
info:eu-repo/semantics/articleVersión
info:eu-repo/semantics/publishedVersionPalabras clave / Materias
Resumen
Background/Aims: The development of new nanomaterials has been growing in recent decades to bring benefits in several areas, especially carbon-based nanoparticles, which have unique physical-chemical properties and ... [+]
Background/Aims: The development of new nanomaterials has been growing in recent decades to bring benefits in several areas, especially carbon-based nanoparticles, which have unique physical-chemical properties and allow to take on several applications. Consequently, the use of new nanomaterials without previous toxicological studies raises concern about possible harmful health effects. The aim of this study was to investigate the cytotoxic profile of a new multi-walled carbon nanotube (MWCNT) functionalized with tetraethylenepentamine called OCNT-TEPA using in vitro assays in murine macrophage cells linage J774 A.1. Methods: OCNT-TEPA was characterized by transmission electron microscopy (TEM) and high resolution TEM (HR-TEM), scanning electron microscopy (SEM), zeta potential and dynamic light scattering (DLS), and its cytotoxic effects were evaluated at 24 and 48 hours by cell viability assays (MTT and NR), morphology and cell recovery (optic microscopy and clonogenic assay), formation of reactive oxygen (ROS) and nitric oxide (NO) species, inflammatory profile (IL-6 and TNF cytokines), mitochondrial membrane potential analysis (MMP), activation of the caspase 3 pathway and cell death (flow cytometry). Results: The data showed a significant decrease in cell viability, increased production of ROS and NO, alteration of mitochondrial membrane potential, increased levels of inflammatory cytokines, alteration of cell morphology, activation of the Caspase 3 pathway and consequently cell death, in the highest concentrations of OCNT-TEPA tested in the periods of 24 and 48 hours. Conclusion: The analyses showed that OCNT-TEPA has a dose-dependent cytotoxic profile, which may be harmful to murine macrophages (J774 A.1) and may represent a health risk. [-]
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Cell Physiol Biochem 2022: 56Entidad financiadora
PETROBRAS | European Union – Next Generation EU, Margarita Salas postdoctoral contract | Fundaçao de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | Financiadora de Estudos e Projetos (FINEP) | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
Código del proyecto o subvención
2017/00010-7 | MGS/2021/21 (UP2021-021) | 2013/07296-2 | 001
Derechos de acceso
Copyright © 2022 The Author(s)
info:eu-repo/semantics/openAccess
info:eu-repo/semantics/openAccess
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