Comparing LD50/LC50 Machine Learning Models for Multiple Species
- 23 February 2023
- journal article
- research article
- Published by American Chemical Society (ACS) in ACS Chemical Health & Safety
- Vol. 30 (2) , 83-97
Abstract
The lethal dose or concentration which kills 50% of the animals (LD50 or LC50) is an important parameter for scientists to understand the toxicity of chemicals in different scenarios that can be used to make go-no-go decisions, and ultimately assist in the choice of the right personal protective equipment needed for containment. The LD50 assessment process has also required the use of many animals although modern methods have reduced the number of rats needed. Since a compound is usually considered highly toxic when the LD50 is lower than 25 mg/kg, such a classification provides potentially valuable safety information to synthetic chemists and other safety assessment scientists. The need for finding alternative approaches such as computational methods is important to ultimately reduce animal use for this testing further still. We now summarize our efforts to use public data for building in vivo LD50 or LC50 classification and regression machine learning models for various species (rat, mouse, fish, and daphnia) and their fivefold cross-validation statistics with different machine learning algorithms as well as an external curated test set for mouse LD50. These datasets consist of different molecule classes, may cover different activity ranges, and also have a range of dataset sizes. The challenges of using such computational models are that their applicability domain will also need to be understood so that they can be used to make reliable predictions for novel molecules. These machine learning models will also need to be backed up with experimental validation. However, such models could also be used for efforts to bridge gaps in individual toxicity datasets. Making such models available also opens them up to potential misuse or dual use. We will summarize these efforts and propose that they could be used for scoring the millions of commercially available molecules, most of which likely do not have a known LD50 or for that matter any data in vitro or in vivo for toxicity.Keywords
Funding Information
- National Institute of Environmental Health Sciences (2R44ES031038-02A1)
- National Institute of General Medical Sciences (2R44GM122196-04A1)
This publication has 72 references indexed in Scilit:
- Estimation of acute oral toxicity in rat using local lazy learningJournal of Cheminformatics, 2014
- In Silico Prediction of Chemical Acute Oral Toxicity Using Multi-Classification MethodsJournal of Chemical Information and Modeling, 2014
- QSAR Modelling of Rat Acute Toxicity on the Basis of PASS PredictionMolecular Informatics, 2011
- Estimation of reliability of predictions and model applicability domain evaluation in the analysis of acute toxicity (LD50)SAR and QSAR in Environmental Research, 2010
- Quantitative Structure−Activity Relationship Modeling of Rat Acute Toxicity by Oral ExposureChemical Research in Toxicology, 2009
- A Novel Two-Step Hierarchical Quantitative Structure–Activity Relationship Modeling Work Flow for Predicting Acute Toxicity of Chemicals in RodentsEnvironmental Health Perspectives, 2009
- Can we estimate the accuracy of ADME–Tox predictions?Drug Discovery Today, 2006
- Prediction of Acute Mammalian Toxicity of Organophosphorus Pesticide Compounds from Molecular StructureSAR and QSAR in Environmental Research, 1999
- Acute oral toxicity.Environmental Health Perspectives, 1998
- Analysis of Structure-Toxicity Relationships for A Series of Amide Herbicides Using Statistical Methods and Neural NetworkSAR and QSAR in Environmental Research, 1996