期刊
TOXICOLOGY MECHANISMS AND METHODS
卷 31, 期 7, 页码 517-530出版社
TAYLOR & FRANCIS LTD
DOI: 10.1080/15376516.2021.1930311
关键词
Nanomaterials; nanoparticles; multi-walled carbon nanotube; cytotoxicity; inflammation; apoptosis; necrosis; murine fibroblast cells
类别
资金
- PETROBRAS [2017/00010-7]
The search for new nanomaterials has provided opportunities for industrial applications, such as carbon nanotubes (CNT), which have excellent properties but may pose health risks. This study investigated the cytotoxicity of a new functionalized multi-walled carbon nanotube (MWCNT) on mouse fibroblast cells, revealing potential inflammatory and cell death effects. These findings highlight the importance of assessing the toxicological profile of nanomaterials for industrial and biological safety.
The search for new nanomaterials has brought to the multifactorial industry several opportunities for use and applications for existing materials. Carbon nanotubes (CNT), for example, present excellent properties which allow us to assume a series of applications, however there is concern in the industrial scope about possible adverse health effects related to constant exposure for inhalation or direct skin contact. Thus, using cell models is the fastest and safest way to assess the effects of a new material. The aim of this study was to investigate the cytotoxic profile in LA9 murine fibroblast lineage, of a new multi-walled carbon nanotube (MWCNT) that was functionalized with tetraethylenepentamine (TEPA) to obtain better physical-chemical characteristics for industrial use. The modifications presented in the CNT cause concern, as they can change its initial characteristics, making this nanomaterial harmful. HR-TEM, FE-SEM and zeta potential were used for the characterization. Cytotoxicity and cell proliferation tests, oxidative and nitrosative stress analyzes and inflammatory cytokine assay (TNF-alpha) were performed. The main findings demonstrated a reduction in cell viability, increased release of intracellular ROS, accompanied by an increase in TNF-alpha, indicating an important inflammatory profile. Confirmation of the data was performed by flow cytometry and ImageXpress with apoptosis/necrosis markers. These data provide initial evidence that OCNT-TEPA has a cytotoxic profile dependent on the concentration of LA9 fibroblasts, since there was an increase in free radicals, inflammation induction and cell death, suggesting that continuous exposure to this nanoparticle can cause damage to different tissues in the organism.
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