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Models for estimating the non-specific toxicity of organic compounds in short-term bioassays

机译:短期生物测定中估计有机化合物非特异性毒性的模型

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摘要

The solvation parameter model is used to construct equations for the estimation of the non-specific toxicity of neutral organic compounds to five organisms used for short-term toxicity testing. For the bacteria Vibrio fischeri (Microtox(TM) test) and Pseudomonas putida, the protozoan Tetrahymena pyriformis (Tetratox test), the green alga Scendesmus quadricauda and the brine shrimp Artemia salina, the main factors resulting in increased non-specific toxicity are size (dominantly) and lone-pair electron interactions, with hydrogen-bond basicity the most important solute property reducing toxicity. Species differences in relative non-specific toxicity are largely related to differences in cohesion and hydrogen-bond acidity of the biomembranes. The models for non-specific toxicity are proposed as an alternative to the octanol-water distribution constant for the determination of baseline toxicity. Failure of the octanol-water distribution constant to model non-specific toxicity is quantitatively explained by its inability to adequately characterize the sorption properties of the biomembranes for compounds with varied properties. [References: 53]
机译:溶剂化参数模型用于构建方程式,以评估中性有机化合物对用于短期毒性测试的五种生物的非特异性毒性。对于细菌弧菌(Microtox(TM)测试)和恶臭假单胞菌(Pseudomonas putida),原生动物Tetrahymena pyriformis原生动物(Tetratox测试),绿藻Scendesmus quadricauda和卤水虾Artemia salina,导致非特异性毒性增加的主要因素是大小( (主要是)和孤对电子相互作用,氢键碱度是最重要的降低毒性的溶质。相对非特异性毒性的物种差异在很大程度上与生物膜的内聚力和氢键酸度的差异有关。建议使用非特异性毒性模型代替辛醇-水分布常数来确定基线毒性。辛醇-水分布常数无法建模非特异性毒性的原因在于,它无法充分表征生物膜对各种特性化合物的吸附特性。 [参考:53]

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