期刊
TOXICOLOGY IN VITRO
卷 28, 期 2, 页码 164-170出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tiv.2013.10.023
关键词
IVIVE; In vitro metabolism; Reverse dosimetry; Css
类别
资金
- American Chemistry Council
- CEFIC Long-Range Research Initiatives [LRI-HBM3-IRAS-0712]
- Doerenkamp-Zbinden Foundation
As part of an effort to support in silico/in vitro based risk assessment, we evaluated the accuracy associated with conducting simple in vitro to in vivo extrapolation (IVIVE) for environmental compounds using available in vitro human metabolism data. The IVIVE approach was applied to a number of compounds with a wide range of properties spanning the diversity of characteristics of environmental compounds, and where possible the resulting estimates of the in vivo steady-state blood concentration were compared with estimates derived on the basis of human in vivo kinetic data. There appears to be a systematic bias in the estimation of intrinsic clearance (Clint) from in vitro versus in vivo data, with in vitro based estimates underestimating in vivo clearance for small values of Clint but with the opposite relationship at large values of Clint. Nevertheless, the resulting estimates of C were in good agreement. The chief drawback of the simple approach used in this study, which performs the IVIVE prediction for the parent compound only, is that it is not applicable for toxicity associated with a metabolite. (C) 2013 Elsevier Ltd. All rights reserved.
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