首页> 外文会议>Micropol amp; Ecohazard 2007 : Book of Abstracts >Plasma levels of non-steroidal anti-inflammatory drugs (NSAIDs) and gemfibrozil in fish exposed to sewage effluents: Assessing the risk of discharges to aquatic environments
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Plasma levels of non-steroidal anti-inflammatory drugs (NSAIDs) and gemfibrozil in fish exposed to sewage effluents: Assessing the risk of discharges to aquatic environments

机译:暴露于污水中的鱼类的血浆中非甾体类抗炎药(NSAID)和吉非贝齐的血浆水平:评估排放到水生环境中的风险

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A model for bioconcentration of Pharmaceuticals was tested by exposing rainbow trout to three sewage effluents and analyzing Pharmaceuticals in their blood. Fish plasma concentrations were compared to human therapeutic plasma concentrations of the drugs to rank the possibility of target interactions. Actual plasma levels of diclofenac, naproxen and gemfibrozil were similar or lower than modelled values, which is acceptable for an early tier test, however ibuprofen levels were >200 times higher than modelled at one site. No bioconcentration of ketoprofen was detected. Diclofenac and gemfibrozil, followed by ibuprofen, are predicted to have the highest risk of target interactions in fish. However, bioconcentration factors varied considerably between sites which could not be attributed to differences in water concentrations, temperatures or exposure time. This suggests that chemical characteristics of effluent and recipient water could be useful to improve models for bioconcentration of Pharmaceuticals in aquatic organisms.
机译:通过将虹鳟鱼暴露于三种污水中并分析其血液中的药物,测试了药物生物富集模型。将鱼的血浆浓度与药物的人治疗性血浆浓度进行比较,以确定靶标相互作用的可能性。双氯芬酸,萘普生和吉非贝齐的实际血浆水平与模型值相近或低于模型值,这在早期测试中是可以接受的,但是布洛芬的水平却比一个地点的模型高200倍以上。未检测到酮洛芬的生物浓缩。预计双氯芬酸和吉非贝齐,然后是布洛芬,在鱼类中具有最高的靶标相互作用风险。但是,不同地点之间的生物浓缩系数差异很大,这不能归因于水浓度,温度或暴露时间的差异。这表明废水和接收水的化学特性可能有助于改善水生生物中药物生物富集的模型。

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