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Enantioselective Acute Toxicity Effects and Bioaccumulation of Furalaxyl in the Earthworm (Eisenia foetida)

机译:worm(Eisenia foetida)中对呋喃草酯的对映选择性急性毒性作用和生物富集

摘要

The enantioselectivities of individual enantiomers of furalaxyl in acute toxicity and bioaccumulation in the earthworm (Eisenia foetida) were studied. The acute toxicity was tested by filter paper contact test. After 48 h of exposure, the calculated LC50 values of the R-form, rac-form, and S-form were 2.27, 2.08, and 1.22 mu g cm(-2), respectively. After 72 h of exposure, the calculated LC50 values were 1.90, 1.54, and 1.00 mu g cm(-2), respectively. Therefore, the acute toxicity of furalaxyl enantiomers was enantioselective. During the bioaccumulation experiment, the enantiomer fraction of furalaxyl in earthworm tissue was observed to deviate from 0.50 and maintained a range of 0.55-0.60; in other words, the bioaccumulation of furalaxyl was enantioselective in earthworm tissue with a preferential accumulation of S-furalaxyl. The uptake kinetic of furalaxyl enantiomers fitted the first-order kinetics well and the calculated kinetic parameters were consistent with the low accumulation efficiency. (C) 2014 Wiley Periodicals, Inc.
机译:研究了呋喃甲酰基个别对映体在acute(Eisenia foetida)的急性毒性和生物积累中的对映选择性。急性毒性通过滤纸接触试验进行测试。暴露48小时后,R形,rac形和S形的LC50计算值分别为2.27、2.08和1.22μg cm(-2)。暴露72小时后,计算出的LC50值分别为1.90、1.54和1.00μg cm(-2)。因此,呋喃基对映体的急性毒性是对映选择性的。在生物富集实验中,earth组织中呋喃草酯的对映异构体分数从0.50偏离并保持在0.55-0.60的范围内。换句话说,在earth组织中呋喃草酰的生物积累是对映选择性的,而S-呋喃草酰的优先积累。呋喃基对映体的吸收动力学很好地拟合了一级动力学,并且所计算的动力学参数与低累积效率一致。 (C)2014威利期刊公司

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