Machine learning-driven nanoparticle toxicity.

Journal: Ecotoxicology and environmental safety
Published Date:

Abstract

This study presents a comprehensive machine learning-driven analysis to understand and predict the toxicity of nanoparticles (NPs), a crucial aspect in ensuring the safe application of nanotechnology in medicine, pharmaceuticals, biotechnology, and various other industries. By using a robust dataset, we deployed Random Forest (RF) and Light Gradient Boosting Machine (LightGBM) algorithms to identify key NP features that significantly influence cellular toxicity. The integration of Shapley Additive exPlanations (SHAP) values provided an interpretative insight into the predictive models, allowing for a quantitative assessment of feature impact. Our findings highlighted the inverse relationship between NP concentration and cell viability and the heightened toxicity of smaller NPs due to their larger surface-to-volume ratios. Notably, the LightGBM model's sensitivity to zeta potential elucidates the nuanced impact of surface charge on cytotoxic effects. The results from this investigation can guide the synthesis of safer NPs, emphasized the need to consider these critical features to mitigate toxicity while maintaining functional integrity. The study underlines the complexity of NP toxicity modeling and the necessity for advanced analytical methods to capture the multifaceted nature of nanomaterial interactions with biological systems. This work lays the groundwork for future research aimed at refining NP design for safer biomedical applications and consumer products, marking a significant step towards responsible nanotechnology development.

Authors

  • Zied Hosni
    Institute for Materials Discovery, University College London, 40 Roberts Building, London WC1E 7 JE, United Kingdom. Electronic address: Z.HOSNI@UCL.AC.UK.
  • Sofiene Achour
    University of Tunis El Manar, Research Unit of Modeling in Fundamental Sciences and Didactics, IPEIEM, PO Box 254, El Manar 2, Tunis 2096, Tunisia; Center for Research in Microelectronics and Nanotechnology (CRMN), TechnopĂ´le de Sousse "Novation City", BP 334 Sahloul Sousse 4054, Sahloul, Tunisia.
  • Fatma Saadi
    Department of Chemistry, Faculty of Science, Northern Border University, Arar, Saudi Arabia.
  • Yangfan Chen
    Guangdong Provincial Key Laboratory of Medical Image Processing, Guangdong Province Engineering Laboratory for Medical Imaging and Diagnostic Technology, School of Biomedical Engineering, Southern Medical University, Guangzhou, Guangdong, China.
  • Mohammed Al Qaraghuli
    Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 161 Cathedral Street, Glasgow G4 0RE, UK; SiMologics Ltd. The Enterprise Hub, Level 6 Graham Hills Building, 50 Richmond Street, Glasgow G1 1XP, UK.