Initial ecological risk assessment of eight selected human pharmaceuticals in Japan.

Hiroshi Yamamoto, Yudai Nakamura, Yuki Nakamura, Chise Kitani, Tetsuya Imari, Jun Sekizawa, Yuji Takao, Naoyuki Yamashita, Narisato Hirai, Shigeto Oda, Norihisa Tatarazako
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Abstract

Eight pharmaceuticals were selected on the basis of their domestic consumption in Japan, the excretion ratio of the parent compound and the frequency of detection in the aquatic environment or wastewater treatment plant effluent. Toxicity tests on these pharmaceuticals were conducted using Japanese medaka (Oryzias latipes), daphnia (Daphnia magna), and green algae (Psuedokirchneriella subcapitata). Predicted no effect concentration (PNEC) was calculated using lethal or effect concentration 50 (LC50 or EC50) values and no effect concentration (NOEC) obtained in the toxicity tests for these compounds. Predicted environmental concentration (PEC) was also calculated from annual consumption, the excretion rate of the parent compound, and removal rate in the preliminary batch activated sludge treatment performed in this study. Maximum concentrations found in the aquatic environment or sewage effluent in Japan or foreign countries were also used for another calculation of PEC. Initial risk assessment on the selected pharmaceuticals was performed using the PEC/PNEC ratio. The results of initial risk assessment on the eight selected pharmaceuticals suggest neither urgent nor severe concern for the ecological risk of these compounds, but further study needs to be conducted using chronic toxicity tests, including reproduction inhibition and endocrine disruption assessments.

日本8种选定的人用药物的初步生态风险评估。
根据其在日本国内的消费量、母体化合物的排泄比例以及在水生环境或污水处理厂流出物中检测到的频率,选择了8种药物。对这些药物进行了毒性试验,使用的是日本水母(Oryzias latipes)、水蚤(daphnia magna)和绿藻(Psuedokirchneriella subcapitata)。预测无效应浓度(PNEC)采用致死或效应浓度50 (LC50或EC50)值计算,无效应浓度(NOEC)在这些化合物的毒性试验中得到。预测环境浓度(PEC)也由年消耗量、母体化合物的排泄率和本研究中进行的初步批量活性污泥处理的去除率计算得出。在日本或国外的水生环境或污水排放中发现的最大浓度也用于另一种PEC计算。采用PEC/PNEC比率对所选药物进行初步风险评估。对选定的八种药物的初步风险评估结果表明,对这些化合物的生态风险既不迫切也不严重关切,但需要通过慢性毒性试验进行进一步研究,包括生殖抑制和内分泌干扰评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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