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The integrated acute systemic toxicity project (ACuteTox) for the optimisation and validation of alternative in vitro tests.
Stockholm University, Faculty of Science, Department of Neurochemistry.ORCID iD: 0000-0001-6298-201X
2007 (English)In: ATLA (Alternatives to Laboratory Animals), ISSN 0261-1929, Vol. 35, no 1, 33-8 p.Article in journal (Refereed) Published
Abstract [en]

The ACuteTox project is designed to replace animal testing for acute systemic toxicity, as is widely used today for regulatory purposes, by using in vitro and in silico alternatives. In spite of the fact that earlier studies on acute systemic toxicity demonstrated a good correlation between in vitro basal cytotoxicity data (the 50% inhibitory concentration [IC50]) in human cell lines and rodent LD50 values, and an even better correlation between IC50 values and human lethal blood concentrations, very few non-animal tests have been accepted for general use. Therefore, the aim of the ACuteTox project is to adapt new testing strategies, for example, the implementation of new endpoints and new cell systems for toxicity screening, organ-specific models, metabolism-dependent toxicity, tissue absorption, distribution and excretion, and computer-based prediction models. A new database, AcuBase, containing descriptions and results of in vitro tests of the 97 reference chemicals, as well as the results of animal experimentation, and human acute toxicity data, will be generated within the framework of ACuteTox. Scientists from 13 European countries are working together and making efforts to find the most appropriate testing strategies for the prediction of human acute systemic toxicity, and also to select a robust in vitro test battery for cytotoxicity testing of chemicals.

Place, publisher, year, edition, pages
2007. Vol. 35, no 1, 33-8 p.
National Category
Natural Sciences
Research subject
Neurochemistry and Molecular Neurobiology
URN: urn:nbn:se:su:diva-32297ISI: 000245500400022PubMedID: 17411349OAI: diva2:279982
Available from: 2009-12-07 Created: 2009-12-07 Last updated: 2015-03-09Bibliographically approved

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