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OECD validation study to assess intra- and inter-laboratory reproducibility of the zebrafish embryo toxicity test for acute aquatic toxicity testing

机译:经合组织验证研究,以评估斑马鱼胚胎毒性试验在实验室内和实验室间的可重复性,以进行急性水生毒性试验

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A The OECD validation study of the zebrafish embryo acute toxicity test (ZFET) for acute aquatic toxicity testing evaluated the ZFET reproducibility by testing 20 chemicals at 5 different concentrations in 3 independent runs in at least 3 laboratories. Stock solutions and test concentrations were analytically confirmed for 11 chemicals. Newly fertilised zebrafish eggs (20/concentration and control) were exposed for 96. h to chemicals. Four apical endpoints were recorded daily as indicators of acute lethality: coagulation of the embryo, lack of somite formation, non-detachment of the tail bud from the yolk sac and lack of heartbeat. Results (LC50 values for 48/96. h exposure) show that the ZFET is a robust method with a good intra- and inter-laboratory reproducibility (CV. <. 30%) for most chemicals and laboratories. The reproducibility was lower (CV > 30%) for some very toxic or volatile chemicals, and chemicals tested close to their limit of solubility. The ZFET is now available as OECD Test Guideline 236.Considering the high predictive capacity of the ZFET demonstrated by Belanger et al. (2013) in their retrospective analysis of acute fish toxicity and fish embryo acute toxicity data, the ZFET is ready to be considered for acute fish toxicity for regulatory purposes.
机译:经合发组织针对斑马鱼胚胎急性毒性试验(ZFET)进行的急性水生毒性试验的验证研究通过在至少3个实验室中以3种独立运行方式对5种不同浓度的20种化学物质进行了测试,从而评估了ZFET的可重复性。分析确定了11种化学药品的储备溶液和测试浓度。将新受精的斑马鱼卵(浓度为20 /对照组)暴露于化学品中96小时。每天记录四个顶端终点,作为急性致死性的指标:胚胎凝结,缺少松果体形成,尾芽未从卵黄囊中脱离和心跳加快。结果(48 / 96.h暴露的LC50值)表明ZFET是一种健壮的方法,对于大多数化学品和实验室,实验室内和实验室间的重现性均良好(CV <30%)。对于某些剧毒或易挥发的化学药品,其重现性较低(CV> 30%),并且所测试的化学药品接近其溶解度极限。 ZFET现在可作为OECD测试指南236获得。考虑到Belanger等人所展示的ZFET的高预测能力。 (2013年)在对急性鱼毒性和鱼胚急性毒性数据的回顾性分析中,出于监管目的,ZFET准备考虑用于急性鱼毒性。

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