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Functionalized Titanium Nanoparticles Induce Oxidative Stress and Cell Death in Human Skin Cells.
Brassolatti, Patricia; de Almeida Rodolpho, Joice Margareth; Franco de Godoy, Krissia; de Castro, Cynthia Aparecida; Flores Luna, Genoveva Lourdes; Dias de Lima Fragelli, Bruna; Pedrino, Matheus; Assis, Marcelo; Nani Leite, Marcel; Cancino-Bernardi, Juliana; Speglich, Carlos; Frade, Marco Andrey; de Freitas Anibal, Fernanda.
Afiliação
  • Brassolatti P; Laboratory of Inflammation and Infectious Diseases, Department of Morphology and Pathology, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
  • de Almeida Rodolpho JM; Laboratory of Inflammation and Infectious Diseases, Department of Morphology and Pathology, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
  • Franco de Godoy K; Laboratory of Inflammation and Infectious Diseases, Department of Morphology and Pathology, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
  • de Castro CA; Laboratory of Inflammation and Infectious Diseases, Department of Morphology and Pathology, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
  • Flores Luna GL; Laboratory of Inflammation and Infectious Diseases, Department of Morphology and Pathology, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
  • Dias de Lima Fragelli B; Laboratory of Inflammation and Infectious Diseases, Department of Morphology and Pathology, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
  • Pedrino M; Laboratory of Inflammation and Infectious Diseases, Department of Morphology and Pathology, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
  • Assis M; Center for the Development of Functional Materials, Department of Chemistry, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
  • Nani Leite M; Division of Dermatology - Wound Healing & Hansen's Disease Lab, Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
  • Cancino-Bernardi J; Nanomedicine and Nanotoxicology Group, Physics Institute of São Carlos, University of São Paulo, São Carlos, São Paulo, Brazil.
  • Speglich C; Leopoldo Américo Miguez de Mello CENPES/Petrobras Research Center, Rio de Janeiro, Rio de Janeiro, Brazil.
  • Frade MA; Division of Dermatology - Wound Healing & Hansen's Disease Lab, Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
  • de Freitas Anibal F; Laboratory of Inflammation and Infectious Diseases, Department of Morphology and Pathology, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
Int J Nanomedicine ; 17: 1495-1509, 2022.
Article em En | MEDLINE | ID: mdl-35388270
ABSTRACT

Purpose:

Nanoparticles are resources of advanced nanotechnology being present in several products. Titanium dioxide nanoparticles are among the five most widely used NP currently expanding their benefits from the oil industry to the areas of diagnostic medicine due to their properties and small size. However, its impact on human health is still controversial in the literature. We aimed to evaluate the cytotoxicity of a new titanium NP functionalized with sodium carboxylic ligand (COOH-Na+) in human keratinocytes (HaCaT) and human fibroblasts (HDFn).

Methods:

The physical-chemical characterization was performed by the transmission electron microscopy (TEM), dynamic light scattering (DLS) and zeta potential techniques, respectively. MTT and LDH assays were used to assess cytotoxicity and cell membrane damage respectively, ELISA to identify the inflammatory profile and, reactive oxygen species assay and cytometry to detect reactive oxygen species and their relationship with apoptosis/necrosis mechanisms.

Results:

The results demonstrated a decrease in cell viability at the highest concentrations tested for both cell lines, but no change in LDH release was detected for the HaCaT. The cell membrane damage was found only at 100.0 µg/mL for the HDFn. It was demonstrated that cytotoxicity in the highest concentrations evaluated for both cell lines for the 72 h period. The HDFn showed damage to the cell membrane at a concentration of 100 µg/mL followed by a significant increase in reactive oxygen species production. No inflammatory profile was detected. The HaCaT showed apoptosis when exposed to the highest concentration evaluated and HDFn showed both apoptosis and necrosis for the same concentration.

Conclusion:

Thus, it is possible to conclude that the cytotoxicity mechanism differs according to the cell type evaluated, with HDFn being the most sensitive line in this case, and this mechanism can be defined in a dose and time dependent manner, since the highest concentrations also triggered death cell.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nanopartículas / Nanopartículas Metálicas Limite: Humans Idioma: En Revista: Int J Nanomedicine Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nanopartículas / Nanopartículas Metálicas Limite: Humans Idioma: En Revista: Int J Nanomedicine Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Brasil