NanoToxRadar: A Multitarget Nano-QSAR Model for Predicting the Cytotoxicity Values of Multicomponent Nanoparticles

Nanotechnological advances have led to the development of nanoparticles with complex structures. In this context, nano-QSAR models have been developed to assess toxicity; however, the applicability domain (AD) of such models is significantly restricted to specific types of nanoparticles (i.e., bare metal oxides, coated metals, or carbon-based nanomaterials) and target cell lines. Accordingly, NanoToxRadar, a web-based platform for predicting the toxicity of multicomponent nanoparticles (MC-NPs) toward various cell lines, was developed to extend the AD of the nano-QSAR model. The size-dependent electron-configuration fingerprint was used to represent the molecular structures of MC-NPs, and one-hot encoded cell types were used to predict toxicities toward 110 cell lines. The CatBoost regression model achieved good performance (R<sup>2</sup> <sub>Test</sub> = 0.877) and was deployed online (https://www.kitox.re.kr/nanotoxradar). The Web site takes the nanoparticle composition of the core as well as the shell, dopant, coating material, and diameter as inputs and predicts pIC<sub>50</sub> values for 110 cell lines.

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Publication Details

Journal
ACS Nanoscience Au
Published
2025-08-08
DOI
https://doi.org/10.1021/acsnanoscienceau.5c00035
Citations
1
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
1.50

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article

NanoToxRadar: A Multitarget Nano-QSAR Model for Predicting the Cytotoxicity Values of Multicomponent Nanoparticles

Suraya Abdul Rashid, Danail Hristozov, Alex Zabeo, Lang Tran et al.
1 citations
ACS Nanoscience Au
Computational Drug Discovery Methods
1.50
article

NanoToxRadar: A Multitarget Nano-QSAR Model for Predicting the Cytotoxicity Values of Multicomponent Nanoparticles

Suraya Abdul Rashid, Danail Hristozov, Alex Zabeo, Lang Tran, Seokjoo Yoon, Costas A. Charitidis, Georgios P. Gakis, Hyun Kil Shin, Jaehyeon Park, Helena Copsey
article en
1 citations

Abstract

Nanotechnological advances have led to the development of nanoparticles with complex structures. In this context, nano-QSAR models have been developed to assess toxicity; however, the applicability domain (AD) of such models is significantly restricted to specific types of nanoparticles (i.e., bare metal oxides, coated metals, or carbon-based nanomaterials) and target cell lines. Accordingly, NanoToxRadar, a web-based platform for predicting the toxicity of multicomponent nanoparticles (MC-NPs) toward various cell lines, was developed to extend the AD of the nano-QSAR model. The size-dependent electron-configuration fingerprint was used to represent the molecular structures of MC-NPs, and one-hot encoded cell types were used to predict toxicities toward 110 cell lines. The CatBoost regression model achieved good performance (R<sup>2</sup> <sub>Test</sub> = 0.877) and was deployed online (https://www.kitox.re.kr/nanotoxradar). The Web site takes the nanoparticle composition of the core as well as the shell, dopant, coating material, and diameter as inputs and predicts pIC<sub>50</sub> values for 110 cell lines.

ACS Nanoscience AuVol. 5(5)
University of Science and Technology (YE), National Technical University of Athens (GR), Korea Institute of Toxicology (KR), Institute of Occupational Medicine (GB), Society of Environmental Toxicology and Chemistry (US), Predictive Biology (United States) (US), Predictive Science (United States) (US), Korea University of Science and Technology (KR)
National Academy of Agricultural Sciences, Ministry of Trade, Industry and Energy, Korea Institute for Advancement of Technology, Korea Institute of Toxicology
Affordable and clean energy
Openalex Percentile: Top 14%
Computational Drug Discovery Methods
1.50
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