ECITTS: An Integrated Approach to the Application of In Vitro Test Systems to the Hazard Assessment of Chemicals,

Author:

Walum Erik1,Balls Michael2,Bianchi Vera3,Blaauboer Bas4,Bolcsfoldi George5,Guillouzo Andre6,Moore Gregory A.7,Odland Lena1,Reinhardt Christoph8,Spielmann Horst9

Affiliation:

1. Unit of Neurochemistry and Neurotoxicology, University of Stockholm, S-106 91 Sweden

2. Department of Human Morphology, University of Nottingham Medical School, Queen's Medical Centre, Nottingham NG7 2UH, UK;

3. Department of Biology, University of Padova, via Trieste 75, 35121 Padova, Italy

4. RITOX, University of Utrecht, P.O. Box 80.176, 3508 TD Utrecht, The Netherlands

5. Safety Assessment, AB Astra, S-151 85 Södertälje, Sweden

6. INSERM, Unité deRecherches Hépatologiques, HopitalPont Chaillou, 35033 Rennes, France

7. National Chemicals Inspectorate, P.O. Box 1384, S-171 27 Solna, Sweden

8. SIAT, ETH-Zentrum, Turnerstrasse 1, 8092 Zürich, Switzerland

9. ZEBET, Robert von Ostertag-Institut, Bundesgesundheitsamt, P.O. Box 33 00 13, W-1000 Berlin 33, Germany

Abstract

As a result of a workshop held at Täljöviken, Åkersberga, Sweden, on 27–29 May 1991, a multicentre collaborative research project was established, with the purpose of developing the concept of integrated in vitro toxicity testing. The first priority was the selection of tests within eight appropriate areas: basal cytotoxicity, irritancy, developmental toxicity, hepatotoxicity, nephrotoxicity, immunotoxicity, neurotoxicity and biokinetics. An ideal battery of tests for each area was identified. Since it was realised that it would not be feasible to include the full ideal list of tests in the project, a minimum test list was also agreed. For each area, ten calibration chemicals were selected. From these 80 compounds, 30 were selected for inclusion, together with 20 of the OECD test programme chemicals, in a first test set of chemicals. The toxicity of these 50 test set chemicals will be investigated in the minimum integrated test scheme. The aim of the project is to employ non-animal methods to assess the toxicological properties of chemicals, and to improve this assessment through the use of knowledge about mechanisms of toxic action. The information produced will contribute to the establishment of a more-scientific and more-efficient toxicological procedure for hazard assessment. Questions concerning which parameters need to be investigated and combined to make hazard assessments, and which parameters relevant to in vivo toxicity can be determined in non-whole animal test systems, will also be addressed.

Publisher

SAGE Publications

Subject

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

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