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盐度对选定的磺胺类药物和甲氧苄啶对普通小球藻毒性的影响。

The influence of salinity on the toxicity of selected sulfonamides and trimethoprim towards the green algae Chlorella vulgaris.

作者信息

Borecka Marta, Białk-Bielińska Anna, Haliński Łukasz P, Pazdro Ksenia, Stepnowski Piotr, Stolte Stefan

机构信息

Department of Environmental Analysis, Faculty of Chemistry, University of Gdańsk, ul. Wita Stwosza 63, 80-308 Gdańsk, Poland.

Department of Environmental Analysis, Faculty of Chemistry, University of Gdańsk, ul. Wita Stwosza 63, 80-308 Gdańsk, Poland.

出版信息

J Hazard Mater. 2016 May 5;308:179-86. doi: 10.1016/j.jhazmat.2016.01.041. Epub 2016 Jan 18.

Abstract

This paper presents the investigation of the influence of salinity variations on the toxicity of sulfapyridine, sulfamethoxazole, sulfadimethoxine and trimethoprim towards the green algae Chlorella vulgaris after exposure times of 48 and 72 h. In freshwater the EC50 values ranged from 0.98 to 123.22 mg L(-1) depending on the compound. The obtained results revealed that sulfamethoxazole and sulfapyridine were the most toxic, while trimethoprim was the least toxic pharmaceutical to the selected organism. Deviations between the nominal and real test concentrations were determined via instrumental analysis to support the interpretation of ecotoxicological data. The toxicity effects were also tested in saline water (3, 6 and 9 PSU). The tendency that the toxicity of selected pharmaceuticals decreases with increasing salinity was observed. Higher salinity implies an elevated concentration of inorganic monovalent cations that are capable of binding with countercharges available on algal surfaces (hydroxyl functional groups). Hence it can reduce the permeability of pharmaceuticals through the algal cell walls, which could be the probable reason for the observed effect. Moreover, for the classification of the mode of toxic action, the toxic ratio concept was applied, which indicated that the effects of the investigated drugs towards algae are caused by the specific mode of toxic action.

摘要

本文介绍了在暴露48小时和72小时后,盐度变化对磺胺吡啶、磺胺甲恶唑、磺胺二甲氧嘧啶和甲氧苄啶对普通小球藻毒性影响的研究。在淡水中,根据化合物的不同,EC50值范围为0.98至123.22 mg L(-1)。所得结果表明,磺胺甲恶唑和磺胺吡啶对所选生物的毒性最大,而甲氧苄啶的毒性最小。通过仪器分析确定标称测试浓度与实际测试浓度之间的偏差,以支持对生态毒理学数据的解释。还在盐水(3、6和9PSU)中测试了毒性效应。观察到所选药物的毒性随盐度增加而降低的趋势。较高的盐度意味着无机单价阳离子浓度升高,这些阳离子能够与藻类表面可用的反电荷(羟基官能团)结合。因此,它可以降低药物通过藻类细胞壁的渗透性,这可能是观察到这种效应的原因。此外,为了对毒性作用模式进行分类,应用了毒性比概念,这表明所研究药物对藻类的影响是由特定的毒性作用模式引起的。

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