<p>Carbon nitride (C<sub>3</sub>N<sub>4</sub>) is a class of nanomaterials that recently became increasingly important in the field of health and biomedicine. However, there is a lack of data regarding its toxicity and how this type of&#xa0;material affects the cells of the innate immune system, such as macrophages. The objective of this study was to evaluate and compare the effect of C<sub>3</sub>N<sub>4</sub> in its pristine and oxidized (oxC<sub>3</sub>N<sub>4</sub>) forms using a monocytic cell line differentiated into macrophages. Human THP-1 cells, differentiated into macrophages, were exposed to increasing concentrations of C<sub>3</sub>N<sub>4</sub> and oxC<sub>3</sub>N<sub>4</sub> (e.g., 10, 50 and 100 µg/mL). The assessment of the overall cytotoxicity, by quantifying intracellular adenosine triphosphate (ATP), apoptosis, change of mitochondrial membrane potential and generation of reactive oxygen species (ROS), was carried out. The results showed a significant decrease in cellular ATP after 48 and 72 h of exposure to both type of nanomaterials. The subsequent staining with annexin V and propidium iodide confirmed a significant increase in cell death induced by oxC<sub>3</sub>N<sub>4</sub>, but not by pristine C<sub>3</sub>N<sub>4</sub>. A significant decrease in mitochondrial membrane potential was also observed only when macrophages were exposed to C<sub>3</sub>N<sub>4</sub>, raising question about the presence of a cell death mechanism not involving mitochondria and masking apoptosis in the case of the oxidized carbon nitride. In addition, in the non-cytotoxic condition, oxC<sub>3</sub>N<sub>4</sub> was able to induce ROS generation. Taken together, our results show that the oxidized form of C<sub>3</sub>N<sub>4</sub> is that affecting more the&#xa0;viability of macrophages.</p>

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Evaluation of the cytotoxicity of pristine two-dimensional carbon nitride and its oxidized form on human macrophages

  • Ghidaa Badran,
  • Tengfei Wang,
  • Yunseok Shin,
  • Sungjin Park,
  • Alberto Bianco

摘要

Carbon nitride (C3N4) is a class of nanomaterials that recently became increasingly important in the field of health and biomedicine. However, there is a lack of data regarding its toxicity and how this type of material affects the cells of the innate immune system, such as macrophages. The objective of this study was to evaluate and compare the effect of C3N4 in its pristine and oxidized (oxC3N4) forms using a monocytic cell line differentiated into macrophages. Human THP-1 cells, differentiated into macrophages, were exposed to increasing concentrations of C3N4 and oxC3N4 (e.g., 10, 50 and 100 µg/mL). The assessment of the overall cytotoxicity, by quantifying intracellular adenosine triphosphate (ATP), apoptosis, change of mitochondrial membrane potential and generation of reactive oxygen species (ROS), was carried out. The results showed a significant decrease in cellular ATP after 48 and 72 h of exposure to both type of nanomaterials. The subsequent staining with annexin V and propidium iodide confirmed a significant increase in cell death induced by oxC3N4, but not by pristine C3N4. A significant decrease in mitochondrial membrane potential was also observed only when macrophages were exposed to C3N4, raising question about the presence of a cell death mechanism not involving mitochondria and masking apoptosis in the case of the oxidized carbon nitride. In addition, in the non-cytotoxic condition, oxC3N4 was able to induce ROS generation. Taken together, our results show that the oxidized form of C3N4 is that affecting more the viability of macrophages.