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细胞毒性药物环磷酰胺和异环磷酰胺在废水和地表水中的存在及归宿

Occurrence and fate of the cytostatic drugs cyclophosphamide and ifosfamide in wastewater and surface waters.

作者信息

Buerge Ignaz J, Buser Hans-Rudolf, Poiger Thomas, Müller Markus D

机构信息

Plant Protection Chemistry, Swiss Federal Research Station (Agroscope), CH-8820 Wädenswil, Switzerland.

出版信息

Environ Sci Technol. 2006 Dec 1;40(23):7242-50. doi: 10.1021/es0609405.

Abstract

The two oxazaphosphorine compounds cyclophosphamide and ifosfamide are important cytostatic drugs used in the chemotherapy of cancer and in the treatment of autoimmune diseases. Their mechanism of action, involving metabolic activation and unspecific alkylation of nucleophilic compounds, accounts for genotoxic effects described in the literature and is reason for environmental concern. The occurrence and fate of cyclophosphamide and ifosfamide were studied in wastewater treatment plants (WWTPs) and surface waters in Switzerland, using a highly sensitive analytical method based on solid-phase extraction and liquid chromatography tandem mass spectrometry. The compounds were detected in untreated and treated wastewater at concentrations of <0.3-11 ng/L, which corresponded well with concentrations predicted from consumption data and typical renal excretion rates. Weekly loads determined in influent and effluent wastewater were comparable and suggested a high persistence in WWTPs. Furthermore, no degradation was observed in activated sludge incubation experiments within 24 h at concentrations of approximately 100 ng/L. Processes that may be relevant for elimination in natural waterbodies were studied with a set of incubation experiments in the laboratory. After extrapolation to natural conditions in surface waters, a slow dark-chemical degradation (half-lives on the order of years) is the most important transformation process. Degradation by photochemically formed HO* radicals may be of some relevance only in shallow, clear, and nitrate-rich waterbodies but could be further exploited for elimination of these compounds by advanced oxidation processes, i.e., in a treatment of hospital wastewater. In surface waters, concentrations ranged from < or =50 to 170 pg/L and were thus several orders of magnitude lower than the levels at which acute ecotoxicological effects have been reported in the literature (mg/L range). However, due to a lack of studies on chronic effects on aquatic organisms and data on occurrence and effects of metabolites, a final risk assessment cannot be made.

摘要

两种恶唑磷化合物环磷酰胺和异环磷酰胺是用于癌症化疗和自身免疫性疾病治疗的重要细胞毒性药物。它们的作用机制涉及代谢活化和亲核化合物的非特异性烷基化,这解释了文献中所述的遗传毒性效应,也是引起环境关注的原因。采用基于固相萃取和液相色谱串联质谱的高灵敏度分析方法,对瑞士污水处理厂(WWTPs)和地表水中环磷酰胺和异环磷酰胺的存在情况及归宿进行了研究。在未经处理和处理后的废水中检测到这些化合物,浓度范围为<0.3 - 11 ng/L,这与根据消费数据和典型肾脏排泄率预测的浓度相当吻合。进出水废水中每周测定的负荷相当,表明它们在污水处理厂中具有很高的持久性。此外,在浓度约为100 ng/L的活性污泥培养实验中,24小时内未观察到降解现象。通过一系列实验室培养实验研究了在天然水体中可能与消除有关的过程。外推至地表水的自然条件后,缓慢的暗化学降解(半衰期为数年)是最重要的转化过程。光化学形成的HO*自由基引起的降解可能仅在浅、清澈且富含硝酸盐的水体中具有一定相关性,但可通过高级氧化过程进一步用于消除这些化合物,即用于医院废水处理。在地表水中,浓度范围为<或 =50至170 pg/L,因此比文献中报道的急性生态毒理学效应水平(mg/L范围)低几个数量级。然而,由于缺乏对水生生物慢性影响的研究以及代谢物的存在和影响数据,无法进行最终的风险评估。

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