恩替卡韦在鱼腥藻、新藻微囊藻、盐水文昌鱼和草履虫中的生态毒性

IF 3.4
Cléssius R. de Souza*, Gabriel Souza-Silva, Fernanda V. M. Silva, Paula von R. Cardoso, Maria Clara V. M. Starling, Walter S. Lima, Cíntia A. J. Pereira, Marcos P. G. Mol and Micheline R. Silveira, 
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引用次数: 0

摘要

世界范围内的药物消费量呈指数增长,随之而来的是环境中这些污染物的增加。本研究旨在评估用于治疗乙型肝炎的抗病毒药物恩替卡韦(ETV)对费氏alivibrio fischeri, novacemicrocystis novacekii, Artemia salina和Biomphalaria glabrata模型的生态毒性,其直接干扰酶促过程和蛋白质合成,可能影响环境和人类健康。在生态毒理学试验中,根据所使用的模型,生物体每隔30分钟至96小时暴露于0至300毫克/升的ETV浓度。只有浓度低于100毫克/升的毒性结果才被认为与环境有关。采用剂量-反应回归对salina、M. novacekii和B. glabrata模型进行统计分析。采用Kruskal-Wallis检验评估光斑白僵菌模型的死亡率。对于含有费氏弧菌的模型,在Microtox标准程序下,以R2测定指数作为拟合参考,考虑相对于对照组(不含ETV的样品)的平均生物发光值在对数尺度上进行分析。所有分析均采用显著性水平5%。暴露于ETV的生物模型在环境相关浓度(100 mg/L)下均未显示出毒性。虽然看起来ETV不构成风险环境由于其低ecotoxicological光谱,由于缺乏的模型中观察到的毒性测试和ETV的nondetection环境,合理使用,处理,治疗,和最终处置药品浪费这种药物,药品垃圾的监测污水和水处理系统,这些系统的改进应该鼓励减轻可能的环境、经济、对健康的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ecotoxicity of Entecavir in Aliivibrio fischeri, Microcystis novacekii, Artemia salina, and Biomphalaria glabrata

The worldwide consumption of medicines has increased exponentially with a consequent increase of these pollutants in the environment. This study aimed to evaluate the ecotoxicity of entecavir (ETV), an antiviral used to treat hepatitis B, in models of Aliivibrio fischeri, Microcystis novacekii, Artemia salina, and Biomphalaria glabrata, which directly interferes with enzymatic processes and protein synthesis, possibly impacting the environment and human health. In the ecotoxicological tests, the organisms were exposed to ETV concentrations ranging from 0 to 300 mg/L at 30 min to 96 h intervals, depending on the model used. Only toxicity results at concentrations below 100 mg/L were considered environmentally relevant. Statistical analyses for the A. salina, M. novacekii, and B. glabrata models were conducted using dose–response regressions. Mortality in the B. glabrata model was assessed using the Kruskal–Wallis test. For the model with A. fischeri, the analyses were performed considering the mean bioluminescence values against the control (sample without ETV) on a logarithmic scale with the R2 determination index as the reference for the fit under the standard Microtox procedure. A significance level of 5% was adopted for all analyses. None of the biological models exposed to ETV showed toxicity at environmentally relevant concentrations (<100 mg/L). Although it may seem that ETV does not pose a risk to the environment due to its low ecotoxicological spectrum, given the lack of toxicity observed in the models tested and the nondetection of ETV in the environment, the rational use, disposal, treatment, and final disposal of pharmaceutical waste of this drug, the monitoring of pharmaceutical waste in sewage and water treatment systems and the improvement of these systems should be encouraged to mitigate possible environmental, economic, and health impacts.

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