Abstract
It is an important precept that, prior to the introduction of new chemicals or products into commerce, they be evaluated for their potential to produce adverse effects. Thus, the art and science of toxicology has been evolving and will continue to evolve in order to detect and define the biologic effects of the chemicals in our environment. For this purpose an impressive array of animal tests and procedures have been described and formalized that attempt to simulate the conditions of human exposure so that adverse effects might be identified and thus avoided. At the same time, many of these same animal models are further utilized to define and describe the mechanism of action of these chemicals. The protocols for a safety program can, therefore, be many and varied, but the hallmarks of design and planning are the selection of relevant routes of exposure in order to investigate acute, subchronic and chronic effects. In all cases, the intent of the toxicologist is to provide a measure of exaggeration in order to assure an adverse effect and then to describe a dose-response relationship and a no-effect level. If the process is successful and the relevant exposure parameters are known, it is often possible to formulate a risk assessment for human exposures.
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© 1987 ECSC, EEC, EAEC, Brussels-Luxembourg and WHO, Geneva
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Buehler, E.V. (1987). Prospective Modeling for Delayed Contact Hypersensitivity. In: Berlin, A., Dean, J., Draper, M.H., Smith, E.M.B., Spreafico, F. (eds) Immunotoxicology. Developments in Hematology and Immunology, vol 16. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-4307-0_31
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DOI: https://doi.org/10.1007/978-94-009-4307-0_31
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