Brake wear (nano)particle characterization and toxicity on airway epithelial cells in vitro

TL;DR

This study characterizes brake wear particles, especially nanoparticles, revealing their composition and demonstrating their potential toxicity to human lung cells, highlighting a health risk from non-exhaust vehicle emissions.

Contribution

It provides detailed analysis of brake wear particles' composition, size distribution, and toxicity, emphasizing the significance of metallic nanoparticles in lung cell damage.

Findings

Nano-sized brake wear particles constitute 26% of total BWP mass.

Nano particles induce reactive oxygen species and reduce cell viability.

Toxicity of nano fraction is comparable to whole BWP, particle size independent.

Abstract

Particulate air pollution results from different sources, among which those related to road traffic have a significant impact on human health. Combustion-derived particles emitted by thermal engines have been incriminated and are now better controlled. In contrast, non-exhaust emission sources related to car wear and degradation processes are not yet regulated. Here we report on brake wear particles (BWP) harvested in two test facilities operating in France, providing samples from different braking systems and driving/testing conditions. Using a combination of light scattering, X-ray fluorescence, optical and electron microscopy, the particle size and elemental composition are revealed. The BWP are shown to be in the nano- to micrometer range and to have a low carbonaceous content (6%), iron and copper being the main components (> 40%). To evaluate the toxicity potential of its nano-sized fraction, brake wear nanoparticles are isolated by sonication, filtration and ultra-centrifugation techniques, leading to stable colloidal dispersions. A significant outcome of this study is that the nano-sized fraction represents 26% by mass of the initial BWP. Human bronchial epithelial cells (Calu-3) are used as relevant target cells to investigate their cytotoxicity. We observe a clear short-term loss of viability associated to reactive oxygen species generation, but with limited pro-inflammatory effects. On an actual cell-deposited mass-dose basis, the cytotoxicity of the nanosized fraction is similar to that of BWP, suggesting that the cytotoxicity is particle size independent. To conclude, brake wear dust contains substantial amount of metallic nanoparticles exhibiting toxicity for lung cells, and should warrant further consideration.