The applicability of in vitro-derived data in hazard identification and characterisation of chemicals

被引:34
作者
Blaauboer, BJ [1 ]
机构
[1] Univ Utrecht, Div Toxicol, RITOX, Inst Risk Assessment Sci, NL-3508 TD Utrecht, Netherlands
关键词
toxicological risk assessment; in vitro methods; integrated testing;
D O I
10.1016/S1382-6689(01)00120-X
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Toxicological hazard and risk assessments for chemicals presently are mainly based on highly standardised protocols for animal experimentation and exposure assessment. In this paper the possibilities are being discussed of developing systems in which the systemic (acute and chronic) toxicity of chemicals can be quantified, without the heavy reliance on animal experiments. On the basis of a chemical's structure, in vitro data on its toxicity, and biokinetic modelling a decision/flow scheme is presented. Key elements are the evaluation of chemical functionalities representing structural alerts for toxic actions, the construction of biokinetic models on the basis of non-animal data (e.g. tissue-blood partition coefficients (PCs), in vitro biotransformation parameters), tests or batteries of tests for determining basal cytotoxicity and more specific tests for evaluating tissue- or organ toxicity. It is concluded that such a flow chart is a useful tool for different steps in the toxicological hazard and risk assessment, especially for those forms of toxicity for which validated in vitro and other non-animal tests have already been developed. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:213 / 225
页数:13
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