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Carbon nanotubes: Structural defects as stressors inducing lung cell toxicity
Rossella Daniela Bengalli1, Giuseppe Zerbi2, Andrea Lucotti2
1POLARIS Research Centre, Dept. of Earth and Environmental Sciences, University of Milano-Bicocca, Piazza della Scienza 1, 20126, Milano, Italy.
Chemico-Biological Interactions
|June 23, 2023
Summary
Structural defects in carbon nanotubes (CNTs) significantly increase their lung toxicity by generating more reactive oxygen species (ROS). The D/G ratio from Raman spectroscopy can predict CNT toxicity and indicate their persistence in lung cells.
Area of Science:
- Nanomaterial safety
- Toxicology
- Materials science
Background:
- Lung toxicity of carbon nanotubes (CNTs) is a significant concern.
- The precise mechanisms underlying CNT toxicity remain incompletely understood.
- Structural defects are hypothesized to play a role in CNT-induced toxicity.
Purpose of the Study:
- To investigate the role of structural defects in CNTs as stressors triggering toxicity.
- To correlate CNT structural defects with their oxidative potential and cellular effects.
- To evaluate the potential of Raman spectroscopy as a predictive tool for CNT toxicity.
Main Methods:
- Characterization of four commercial CNTs using Transmission Electron Microscopy (TEM).
- Quantification of structural defects via Raman spectroscopy (D/G intensity ratio, ID/IG).
- Assessment of oxidative potential using cytochrome-c assay and reactive oxygen species (ROS) detection.
Main Results:
- CNTs with higher structural defect levels (higher ID/IG) exhibited increased ROS generation.
- Higher ROS levels correlated with greater cytotoxicity and cellular damage observed via TEM.
- Raman analysis confirmed the biopersistence of CNTs within lung cells without spectral alteration.
Conclusions:
- The intensity ratio ID/IG serves as a reliable predictive marker for CNT lung toxicity.
- Structural defects are key stressors contributing to CNT-induced oxidative stress and cytotoxicity.
- CNTs demonstrate biopersistence in lung cells, highlighting the importance of understanding defect-mediated toxicity.

