Background
Although substantial concerns about the inflammatory effects of engineered nanomaterial (ENM) have been raised, experimentally assessing toxicity of various ENMs is challenging and time-consuming. Alternatively, quantitative structure-activity relationship (QSAR) models have been employed to assess nanosafety. However, no previous attempt has been made to predict the inflammatory potential of ENMs. Objectives: By employing metal oxide nanoparticles (MeONPs) as a model ENM, we aimed to develop QSAR models for prediction of the inflammatory potential by their physicochemical properties.
Conclusions
IL-1βIL-1β<math><mrow><mtext>IL-</mtext><mn>1</mn><mi>β</mi></mrow></math> released in THP-1 cells can be an index to rank the inflammatory potential of MeONPs. QSAR models based on IL-1βIL-1β<math><mrow><mtext>IL-</mtext><mn>1</mn><mi>β</mi></mrow></math> were able to predict the inflammatory potential of MeONPs. Our approach overcame the challenge of time- and labor-consuming biological experiments and allowed for computational assessment of MeONP inflammatory potential by characterization of their physicochemical properties. https://doi.org/10.1289/EHP6508.
Methods
We built a comprehensive data set of 30 MeONPs to screen a proinflammatory cytokine interleukin (IL)-1 beta (IL-1βIL-1β<math><mrow><mtext>IL-</mtext><mn>1</mn><mi>β</mi></mrow></math>) release in THP-1 cell line. The in vitro hazard ranking was validated in mouse lungs by oropharyngeal instillation of six randomly selected MeONPs. We established QSAR models for prediction of MeONP-induced inflammatory potential via machine learning. The models were further validated against seven new MeONPs. Density functional theory (DFT) computations were exploited to decipher the key mechanisms driving inflammatory responses of MeONPs.
Results
Seventeen out of 30 MeONPs induced excess IL-1βIL-1β<math><mrow><mtext>IL-</mtext><mn>1</mn><mi>β</mi></mrow></math> production in THP-1 cells. In vivo disease outcomes were highly relevant to the in vitro data. QSAR models were developed for inflammatory potential, with predictive accuracy (ACC) exceeding 90%. The models were further validated experimentally against seven independent MeONPs (ACC=86%ACC=86%<math><mrow><mrow><mtext>ACC</mtext><mo>=</mo><mn>86</mn><mo>%</mo></mrow></mrow></math>). DFT computations and experimental results further revealed the underlying mechanisms: MeONPs with metal electronegativity lower than 1.55 and positive ζ-potentialζ-potential<math><mrow><mi>ζ</mi><mtext>-potential</mtext></mrow></math> were more likely to cause lysosomal damage and inflammation. Conclusions: IL-1βIL-1β<math><mrow><mtext>IL-</mtext><mn>1</mn><mi>β</mi></mrow></math> released in THP-1 cells can be an index to rank the inflammatory potential of MeONPs. QSAR models based on IL-1βIL-1β<math><mrow><mtext>IL-</mtext><mn>1</mn><mi>β</mi></mrow></math> were able to predict the inflammatory potential of MeONPs. Our approach overcame the challenge of time- and labor-consuming biological experiments and allowed for computational assessment of MeONP inflammatory potential by characterization of their physicochemical properties. https://doi.org/10.1289/EHP6508.