Machine learning-guided Nano-QSAR modeling predicts HepaRG cell membrane toxicity of engineered nanoparticles with mechanistic insights

Engineered nanoparticles (ENPs), defined as nanoscale materials with at least one dimension between 1 and 100 nm, exhibit multifunctional and tunable physicochemical properties, that are at the center of several innovative fields. However, ENPs may induce a variety of biochemical reactions upon entry into organisms that could be a threat to human health. Therefore, a systematic evaluation of the toxicity of ENPs is essential. Quantitative structure-activity relationship (QSAR) is a practical in vitro modeling approach used to evaluate the toxicity of nanoparticles. In this study, we established the nanometric QSAR (Nano-QSAR) modelling based on cell membrane damage of ENPs to HepaRG cells. The toxicity data of ENPs and related 2D descriptor information were collected from the NanoCommons Knowledge Base. Periodic table descriptors of the elements were calculated using the Elemental Descriptor Calculator software. A multiple linear regression (MLR) model was constructed, and subsequently combined with read-across (RA) descriptors to establish the Nano-quantitative read-across structure-activity relationship (Nano-q-RASAR) model. Furthermore, machine learning (ML) algorithms were applied to optimize the predictive performance of the models. All models were validated according to the stringent OECD QSAR validation guidelines. Finally, a series of true external ENPs without experimental values were autonomously designed, and predicted using the best GB-Nano-QSAR model. Overall, this study can provide efficient and reliable predictions for the cell membrane damage of ENPs and a detailed theoretical explanation of their toxicity mechanism, which is of practical value for the toxicity assessment of ENPs.

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Journal
Cell Biology and Toxicology
Published
2026-01-29
DOI
https://doi.org/10.1007/s10565-026-10144-9
Primary Topic
Computational Drug Discovery Methods
Type
article
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article

Machine learning-guided Nano-QSAR modeling predicts HepaRG cell membrane toxicity of engineered nanoparticles with mechanistic insights

Zhong Ru-gang, Guohui Sun, Ting Ren, Shuo Chen et al.
Cell Biology and Toxicology
Computational Drug Discovery Methods
article

Machine learning-guided Nano-QSAR modeling predicts HepaRG cell membrane toxicity of engineered nanoparticles with mechanistic insights

Zhong Ru-gang, Guohui Sun, Ting Ren, Shuo Chen, Shen Ning, Na Zhang, Xinyu Hao, Lijiao Zhao
article en

Abstract

Engineered nanoparticles (ENPs), defined as nanoscale materials with at least one dimension between 1 and 100 nm, exhibit multifunctional and tunable physicochemical properties, that are at the center of several innovative fields. However, ENPs may induce a variety of biochemical reactions upon entry into organisms that could be a threat to human health. Therefore, a systematic evaluation of the toxicity of ENPs is essential. Quantitative structure-activity relationship (QSAR) is a practical in vitro modeling approach used to evaluate the toxicity of nanoparticles. In this study, we established the nanometric QSAR (Nano-QSAR) modelling based on cell membrane damage of ENPs to HepaRG cells. The toxicity data of ENPs and related 2D descriptor information were collected from the NanoCommons Knowledge Base. Periodic table descriptors of the elements were calculated using the Elemental Descriptor Calculator software. A multiple linear regression (MLR) model was constructed, and subsequently combined with read-across (RA) descriptors to establish the Nano-quantitative read-across structure-activity relationship (Nano-q-RASAR) model. Furthermore, machine learning (ML) algorithms were applied to optimize the predictive performance of the models. All models were validated according to the stringent OECD QSAR validation guidelines. Finally, a series of true external ENPs without experimental values were autonomously designed, and predicted using the best GB-Nano-QSAR model. Overall, this study can provide efficient and reliable predictions for the cell membrane damage of ENPs and a detailed theoretical explanation of their toxicity mechanism, which is of practical value for the toxicity assessment of ENPs.

Cell Biology and ToxicologyVol. 42(1)
Beijing University of Technology (CN), Beijing University of Chemical Technology (CN), University of Science and Technology Beijing (CN)
Openalex Percentile: Top 71%
Computational Drug Discovery Methods
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