SbD4Skin by EosCloud: Integrating multi-view molecular representation for predicting skin sensitization, irritation, and acute dermal toxicity

Assessing chemical toxicity is essential for understanding potential risks to human health. However, ethical, financial, and scientific challenges have driven the demand for non-animal testing methods. This study introduces a computational framework that leverages diverse molecular representations, including MACCS keys, Morgan fingerprints, and Mordred descriptors, to predict skin sensitization, irritation/corrosion, and acute dermal toxicity. Different molecular representations for skin toxicity-related endpoints were first evaluated using three machine learning algorithms (Random Forest, Support Vector Machine, and k-Nearest Neighbors), then combined into a unified input space for training a fully connected neural network (FCNN). Comparative analyses indicate that this multi-view FCNN model offers superior or comparable predictive performance relative to single-representation models, achieving area under the curve (AUC) values of up to 0.91 for irritation/corrosion, 0.88 for sensitization, and 0.82 for acute dermal toxicity on test sets. Additional validation on known toxicants further confirms the framework's robustness, correctly identifying 0.86 of skin sensitizers, 0.89 of irritants, and 0.86 of dermally toxic compounds. Shapley Additive exPlanation (SHAP) analyses highlight the most influential molecular features, providing mechanistic insights and enhancing model transparency. To promote broader adoption and reduce reliance on animal testing, the developed models are freely available through the SbD4Skin (Safe by Design for Skin) web platform (https://eoscloud.entelos.eu/ssbd4chem/sbd4skin/), offering a user-friendly tool for chemical risk assessment and regulatory decision-making. The dataset and model developed in this study have been FAIRified and made available in machine-actionable and modelling-ready formats, supporting transparency, reuse, and regulatory acceptance.

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Publication Details

Journal
Computational and Structural Biotechnology Journal
Published
2025-01-01
DOI
https://doi.org/10.1016/j.csbj.2025.08.001
Citations
1
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
1.50

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article

SbD4Skin by EosCloud: Integrating multi-view molecular representation for predicting skin sensitization, irritation, and acute dermal toxicity

Andreas Tsoumanis, Konstantinos D. Papavasileiou, Nikoletta-Maria Koutroumpa, Georgia Melagraki et al.
1 citations
Computational and Structural Biotechnology Journal
Computational Drug Discovery Methods
1.50
article

SbD4Skin by EosCloud: Integrating multi-view molecular representation for predicting skin sensitization, irritation, and acute dermal toxicity

Andreas Tsoumanis, Konstantinos D. Papavasileiou, Nikoletta-Maria Koutroumpa, Georgia Melagraki, Dimitra‐Danai Varsou, Milica Velimirović, Anastasios G. Papadiamantis, Eleni Papadopoulou, Panagiotis D. Kolokathis, Antreas Afantitis, Μαρία Αντωνίου
article en
1 citations

Abstract

Assessing chemical toxicity is essential for understanding potential risks to human health. However, ethical, financial, and scientific challenges have driven the demand for non-animal testing methods. This study introduces a computational framework that leverages diverse molecular representations, including MACCS keys, Morgan fingerprints, and Mordred descriptors, to predict skin sensitization, irritation/corrosion, and acute dermal toxicity. Different molecular representations for skin toxicity-related endpoints were first evaluated using three machine learning algorithms (Random Forest, Support Vector Machine, and k-Nearest Neighbors), then combined into a unified input space for training a fully connected neural network (FCNN). Comparative analyses indicate that this multi-view FCNN model offers superior or comparable predictive performance relative to single-representation models, achieving area under the curve (AUC) values of up to 0.91 for irritation/corrosion, 0.88 for sensitization, and 0.82 for acute dermal toxicity on test sets. Additional validation on known toxicants further confirms the framework's robustness, correctly identifying 0.86 of skin sensitizers, 0.89 of irritants, and 0.86 of dermally toxic compounds. Shapley Additive exPlanation (SHAP) analyses highlight the most influential molecular features, providing mechanistic insights and enhancing model transparency. To promote broader adoption and reduce reliance on animal testing, the developed models are freely available through the SbD4Skin (Safe by Design for Skin) web platform (https://eoscloud.entelos.eu/ssbd4chem/sbd4skin/), offering a user-friendly tool for chemical risk assessment and regulatory decision-making. The dataset and model developed in this study have been FAIRified and made available in machine-actionable and modelling-ready formats, supporting transparency, reuse, and regulatory acceptance.

Computational and Structural Biotechnology JournalVol. 29
National Technical University of Athens (GR), Hellenic Military Academy (GR), Cyprus Institute of Marketing (CY), Flemish Institute for Technological Research (BE), University of Limassol (CY)
European Commission, HORIZON EUROPE Framework Programme
Zero hunger
Openalex Percentile: Top 14%
Computational Drug Discovery Methods
1.50
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