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Toxicological Sciences 69, 125-130 (2002)
Copyright © 2002 by the Society of Toxicology


IN VITRO TOXICOLOGY AND ALTERNATIVE TESTING

Screening of Dioxin-Like Toxicity Equivalents for Various Matrices with Wildtype and Recombinant Rat Hepatoma H4IIE Cells

Peter A. Behnisch*,{dagger},1, Kazunori Hosoe*, Abraham Brouwer{ddagger} and Shin-ichi Sakai{dagger},§

* Life Science Research Laboratories, Kaneka Corporation, Takasago, Hyogo 676-8688, Japan; {dagger} Environment Preservation Center, Kyoto University, Kyoto 606-8501, Japan; {ddagger} Institute of Environmental Studies, Free University of Amsterdam, The Netherlands; and § Research Center for Material Cycles and Waste Management, National Institute for Environmental Studies, Tsukuba, Ibaraki 305-8506, Japan

ABSTRACT

Determination of dioxin-like compounds utilizing in vitro bioassays such as ethoxyresorufin-O-deethylase (EROD) or chemical-activated luciferase expression (DR-CALUX®) is an important tool to evaluate their Ah receptor-mediated toxic effects. The aim of this study is to describe advantages and limitations of these bioassays using rat hepatoma (H4IIE) wildtype and recombinant H4IIE cells in a 96 well microtiter plate format. We are using these bioassays for the evaluation of relative responses (REP) from several congeners of dioxins (e.g., 2,3,4,7,8-PCDF) or dioxin-like compounds (PCB-126, 2,3,4,7,8-PBDF) to 2,3,7,8-TCDD. In addition, total toxic equivalency factors (TEFs) of mixtures of these dioxin-like compounds from several kinds of matrices such as feed, sediment, or thermal waste residues are measured by both bioassays and additional chemical analysis. These samples were measured in a cross-validation study between two laboratories using the DR-CALUX technology in comparison to the H4IIE-EROD assay and chemical analysis. Improvement of the quality criteria of the newly developed DR-CALUX bioassays in comparison to the EROD bioassay was demonstrated (higher coefficient of determination r2; better repeatability of TCDD and samples), while induction factor, limit of detection, and limit of quantification have been similar. The tested samples showed positive responses in both bioassays using different kinetics (EROD: 72 h; DR-CALUX: 24 h). Ratio of measured toxicity equivalent (TEQ) values varied around mean values of 0.89 (comparing both DR-CALUX laboratories, ranging from 0.68–3.1), 2.0 (comparing EROD and DR-CALUX, ranging from 0.57–8.1), and 1.6–2.5 (comparing EROD-TEQ and I-TEQ, mean 1.6, ranging from 1.0–3.9; for DR-CALUX/I-TEQ, 2.5; 0.61–8.3), respectively. This demonstrates that these bioassays can be used as alternative screening technology for monitoring I-TEQ values in various standards and matrices.

Key Words: Ah receptor; biomarker; CALUX; dioxins; EROD; feed; fly ash; HAH; TCDD; sediments; toxic equivalency factors.


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