Pulmonary Toxicity of Boron Nitride Nanomaterials Is Aspect Ratio Dependent

Abstract

Boron nitride (BN) nanomaterials have drawn a lot of interest in the material science community. However, extensive research is still needed to thoroughly analyze their safety profiles. Herein, we investigated the pulmonary impact and clearance of two-dimensional hexagonal boron nitride ( h -BN) nanosheets and boron nitride nanotubes (BNNTs) in mice. Animals were exposed by single oropharyngeal aspiration to h -BN or BNNTs. On days 1, 7, and 28, bronchoalveolar lavage (BAL) fluids and lungs were collected. On one hand, adverse effects on lungs were evaluated using various approaches ( e.g ., immune response, histopathology, tissue remodeling, and genotoxicity). On the other hand, material deposition and clearance from the lungs were assessed. Two-dimensional h -BN did not cause any significant immune response or lung damage, although the presence of materials was confirmed by Raman spectroscopy. In addition, the low aspect ratio h -BN nanosheets were internalized rapidly by phagocytic cells present in alveoli, resulting in efficient clearance from the lungs. In contrast, high aspect ratio BNNTs caused a strong and long-lasting inflammatory response, characterized by sustained inflammation up to 28 days after exposure and the activation of both innate and adaptive immunity. Moreover, the presence of granulomatous structures and an indication of ongoing fibrosis as well as DNA damage in the lung parenchyma were evidenced with these materials. Concurrently, BNNTs were identified in lung sections for up to 28 days, suggesting long-term biopersistence, as previously demonstrated for other high aspect ratio nanomaterials with poor lung clearance such as multiwalled carbon nanotubes (MWCNTs). Overall, we reveal the safer toxicological profile of BN-based two-dimensional nanosheets in comparison to their nanotube counterparts. We also report strong similarities between BNNTs and MWCNTs in lung response, emphasizing their high aspect ratio as a major driver of their toxicity.

In Vitro Toxicity and Modeling Reveal Nanoplastic Effects on Marine Bivalves

“…To validate whether genotoxicity also occurs in bivalves after waterborne exposure ( in vivo ) experiments, we isolated hemocytes from clams exposed to NPs, and similar results were obtained (Figure S6e). Genotoxicity is a crucial end point in assessing the adverse effects of nanoparticles. , Prior research has demonstrated that nanoparticles can potentially impede DNA repair mechanisms, likely due to oxidative stress induced by the excessive accumulation of ROS. , DNA damage can lead to various consequences, including cell mutations, accelerated aging, and different forms of cell death such as necrosis, pyroptosis, and apoptosis. , Consequently, our in vitro cytotoxicity experiments reinforce the hypothesis that the NP exposure concentrations, extrapolated from the waterborne exposure ( in vivo ) experiments, can induce similar cytotoxic response patterns in the immune cells (hemocytes) of marine bivalves ( in vitro ).…”

Two-dimensional nanomaterials induced nano-bio interfacial effects and biomedical applications in cancer treatment

“…On this basis, it is essential to evaluate the pharmacokinetics of 2D NMs to assess their metabolism and excretion [ 188 ]. Traditional pharmacokinetics relies on methods like inductively coupled plasma and Raman spectroscopy to analyze the concentration of 2D NMs over time in blood, organs, urine, and feces [ 189 ]. Nowadays, the in vivo tracking methods have been employed for real-time, non-invasive, and highly sensitive analysis of pharmacokinetics.…”