The influence of modes of action and physicochemical properties of chemicals on the correlation between in vitro and acute fish toxicity data

被引:37
作者
Kramer, Nynke I. [1 ]
Hermens, Joop L. M. [1 ]
Schirmer, Kristin [2 ,3 ]
机构
[1] Univ Utrecht, Inst Risk Assessment Sci, NL-3508 TD Utrecht, Netherlands
[2] Swiss Fed Inst Aquat Sci & Technol, CH-8600 Dubendorf, Switzerland
[3] ETH, Inst Biogeochem & Pollutant Dynam, CH-8092 Zurich, Switzerland
关键词
Acute fish toxicity; Alternatives to animal testing; In vitro-in vivo extrapolation; Cytotoxicity assays; RAINBOW-TROUT HEPATOCYTES; CELL-LINES; COMPARATIVE CYTOTOXICITY; INVITRO CYTOTOXICITY; INDUSTRIAL-CHEMICALS; PIMEPHALES-PROMELAS; ORGANIC-SUBSTANCES; AQUATIC TOXICITY; PROTEIN-BINDING; POLAR NARCOSIS;
D O I
10.1016/j.tiv.2009.07.029
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
New EU legislation is providing an impetus for research aimed at replacing acute fish toxicity testing with in vitro alternatives. In line with such research, the objective of this study was to determine what factors influence the correlation between in vitro and fish toxicity data. Basal cytotoxicity (IC(50)) and acute toxicity data from fathead minnow (LC(50)) of 82 industrial organic chemicals were obtained from the Halle Registry of Cytotoxicity and the US EPA Fathead Minnow Database. A good correlation between IC(50) with LC(50) data was found (r 0.84). Yet, IC(50) data were less sensitive than LC(50) data by an order of magnitude. Using multiple regression analysis, the octanol-water partition coefficient (K(OW)) and the Henry's Law Constant (H) were found to significantly explain the low absolute sensitivity. The mode of action (MOA) of the chemical was found to significantly explain the general variation in the log IC(50)/log LC(50) regression line. These results support the notion that (a) the bioavailability of hydrophobic (high K(OW)) and volatile (high H) chemicals is significantly lower in in vitro assays than in the fish bioassay and (b) multiple cell types and endpoints should be included to mimic the modes of action possible in the whole organism. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1372 / 1379
页数:8
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