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ABSTRACT: Background
Regulatory toxicity values used to assess and manage chemical risks rely on the determination of the point of departure (POD) for a critical effect, which results from a comprehensive and systematic assessment of available toxicity studies. However, regulatory assessments are only available for a small fraction of chemicals.Objectives
Using in vivo experimental animal data from the U.S. Environmental Protection Agency's Toxicity Value Database, we developed a semiautomated approach to determine surrogate oral route PODs, and corresponding toxicity values where regulatory assessments are unavailable.Methods
We developed a curated data set restricted to effect levels, exposure routes, study designs, and species relevant for deriving toxicity values.
SUBMITTER: Aurisano N
PROVIDER: S-EPMC10056221 | biostudies-literature | 2023 Mar
REPOSITORIES: biostudies-literature