The Application of Toxicokinetic Data to Dosage Selection in Toxicology Studies
- 1 March 1994
- journal article
- Published by SAGE Publications in Toxicologic Pathology
- Vol. 22 (2) , 112-123
- https://doi.org/10.1177/019262339402200205
Abstract
Appropriate dosage selection is a key element in the design of toxicology studies and, hence, is the first step in the process of evaluating the safety of a new chemical or pharmaceutical agent. This demands careful consideration of exposure to the drug or chemical under investigation in relation to the pharmacological or toxicological effects it evokes in an experimental animal. Toxicokinetic data provide this perspective, but they should not be considered exclusively of other data which reflect the specific activity, potency, or metabolism of the drug or chemical in each individual test species. It is equally inappropriate to base dosage selection in toxicology studies exclusively on functional or morphological endpoints that cause effects outside the range which can be accommodated by homeostatic mechanisms and repair processes. Finally, extrapolation of toxicokinetic data across species lines can lead to serious miscalculations with respect to both dosage selection and the process of risk assessment. In each case, decisions should be based on the integration of toxicokinetic data with other measures and endpoints of biological and toxicological effect.Keywords
This publication has 13 references indexed in Scilit:
- Dose selection for animal carcinogenicity studies: a practitioner's perspectiveChemical Research in Toxicology, 1992
- What is an appropriate measure of exposure when testing drugs for carcinogenicity in rodents?Toxicology and Applied Pharmacology, 1992
- An appreciation of the maximum tolerated dose: An inadequately precise decision point in designing a carcinogenesis bioassay?Teratogenesis, Carcinogenesis, and Mutagenesis, 1991
- Interspecies comparisons in toxicology: The utility and futility of plasma concentrations of the test substanceRegulatory Toxicology and Pharmacology, 1990
- Estimating the risk of liver cancer associated with human exposures to chloroform using physiologically based pharmacokinetic modelingToxicology and Applied Pharmacology, 1990
- Physiologically based pharmacokinetics and the risk assessment process for methylene chlorideToxicology and Applied Pharmacology, 1987
- Pharmacokinetics and Toxicity TestingCRC Critical Reviews in Toxicology, 1984
- Pharmacokinetic Considerations in Toxicity TestingDrug Metabolism Reviews, 1982
- Resolution of dose-response toxicity data for chemicals requiring metabolic activation: Example?Vinyl chloride*1Toxicology and Applied Pharmacology, 1978
- Kinetics of Reactive Metabolites and Covalent Binding in Vivo and in VitroPublished by Springer Nature ,1977