The Necessity of Biokinetic Information in the Interpretation of In Vitro Toxicity Data

Author:

Blaauboer Bas J.1

Affiliation:

1. Institute for Risk Assessment Sciences (IRAS), Division of Toxicology, Utrecht University, P.O. Box 80.176, 3508 TD Utrecht, The Netherlands

Abstract

Data derived from in vitro toxicity studies are not directly applicable in an assessment of the toxicity of compounds in intact organisms. The major limitation is the lack of knowledge of biokinetic behaviour in vivo. Since the toxicity of a compound will be determined by the critical concentration (or other dose metric) of the critical compound (or a metabolite thereof) at the critical site of toxic action, biokinetic behaviour must be taken into account. Possibilities of biokinetic modelling on the basis of in vitro and other non-animal data are discussed, and the application of the results in hazard and risk-assessment schedules is considered.

Publisher

SAGE Publications

Subject

Medical Laboratory Technology,Toxicology,General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference43 articles.

1. OECD (1993). Guidance Document for the Development of OECD Guidelines for the Testing of Chemicals. Environment Monograph No. 76, 28 pp. Paris, France: OECD.

2. RussellW.S. & BurchR.L. (1959). The Principles of Humane Experimental Technique, 238 pp. London, UK: Methuen.

3. Council of Europe (1986). European Convention for the Protection of Vertebrate Animals used for Experimental and Other Scientific Purposes, ETS No. 123, 59 pp. Strasbourg, France: Council of Europe.

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