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首页> 外文期刊>The International Journal of Environmental Studies >Pharmaceutical residues: concentration evaluation and risk assessment based on the sales of human drugs in Estonia in 2010
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Pharmaceutical residues: concentration evaluation and risk assessment based on the sales of human drugs in Estonia in 2010

机译:药物残留:基于爱沙尼亚2010年人用药物的销售的浓度评估和风险评估

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摘要

Although the growth in sales of Pharmaceuticals could be taken as a sign of the availability of medical services and medicine, it also indicates an increasing input of drug residues to the environment via treated sewage water. In this paper the medicine consumption in mass units was calculated on the basis of the sale of Pharmaceuticals in 2010. Eleven active substances (ASs) were selected for risk assessment according to the Swedish model. The predicted environmental concentration (PEC) for each AS was calculated and divided by the predicted no-effect concentration. Additionally, hazardous properties were taken into consideration. The calculated values of amoxicil-lin (PEC = 0.24-1.43 μg/l), diclofenac (PEC = 0.2-0.59 μg/l), ciprofloxacin (PEC = 0.052-0.13 μg/l), and ethinyl estradiol (PEC = 0.3 × 10~(-3) μg/l) reflect a high level of risk to the aquatic environment in the area.
机译:尽管药品销售的增长可以看作是获得医疗服务和药品的标志,但它也表明通过处理后的污水向环境中投放的药品残留量正在增加。在本文中,以2010年药品销售为基础,以质量单位计算药品消费量。根据瑞典模型,选择了11种活性物质(ASs)进行风险评估。计算每个AS的预测环境浓度(PEC),并将其除以预测无效浓度。此外,还考虑了危险特性。阿莫西林(PEC = 0.24-1.43μg/ l),双氯芬酸(PEC = 0.2-0.59μg/ l),环丙沙星(PEC = 0.052-0.13μg/ l)和乙炔雌二醇(PEC = 0.3× 10〜(-3)μg/ l)反映了该地区水生环境的高度危险。

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