SCNU Environmental Research Institute, Guangdong Provincial Key Laboratory of Chemical Pollution and Environmental Safety & MOE Key Laboratory of Theoretical Chemistry of Environment, South China Normal University, Guangzhou 510006, China; School of Environment, South China Normal University, University Town, Guangzhou 510006, China.
Department of Environmental Sciences, University of California Riverside, Riverside, CA 92507, USA.
Environ Int. 2021 Aug;153:106543. doi: 10.1016/j.envint.2021.106543. Epub 2021 Apr 2.
Anticancer drugs are a group of therapeutic agents used to enhance cell death in targeted cell types of neoplasia. Because of frequent use and eventual discharge, they have been often detected in wastewater from pharmaceutical factories and hospitals, domestic wastewater, and surface waters. The occurrence of these drugs in aquatic ecosystems and their effects on aquatic organisms have been poorly characterized. This review focuses on the global occurrence of major classes of anticancer drugs in water and sediments of freshwater ecosystems and their ecotoxicological effects at different biological levels. While the availability of data is fairly limited, concentrations of most anticancer drugs range from < 2 ng/L to 762 µg/L in receiving water, while levels in sediments and sludge vary from 0.25 to 42.5 µg/kg. Their detection frequencies were 58%, 52% (78%) and 59% in hospital wastewater, wastewater treatment plant effluents (influents) and surface water, respectively. Predicted log K values of vincristine, imatinib mesylate and tamoxifen are higher than 3 and have estimated half-lives>60 d in waters using quantitative structure-activity relationship models, indicating high potential for persistence and bioaccumulation. Based on a species sensitivity distribution evaluation of 9 compounds, crustaceans are most sensitive to anticancer drugs. The most hazardous compound is cisplatin which has a hazard concentration at the 5th percentile. For Daphnia magna, the acute toxicities of major classes of anticancer drugs are ranked as platinum complexes > endocrine therapy agents > antibiotics > antimetabolite agents > alkylating agents. Using hazard quotient analysis based primarily on the lowest observed effect concentrations (LOECs), cyclophosphamide, cisplatin, 5-fluorouracil, imatinib mesylate, bicalutamide, etoposide and paclitaxel have the highest hazard for aquatic organisms. Further research is needed to identify appropriate chronic endpoints for risk assessment thresholds as well as to better understand the mechanisms of action and the potential multigenerational toxicity, and trophic transfer in ecosystems.
抗癌药物是一组用于增强肿瘤靶向细胞类型细胞死亡的治疗剂。由于经常使用和最终排放,它们经常在制药厂和医院的废水、生活污水和地表水以及环境中被检测到。这些药物在水生生态系统中的出现及其对水生生物的影响尚未得到充分描述。本综述重点介绍了全球抗癌药物在淡水生态系统的水和沉积物中的存在情况及其在不同生物水平上的生态毒理学效应。虽然可用数据相当有限,但大多数抗癌药物在受纳水体中的浓度范围为<2ng/L 至 762µg/L,而沉积物和污泥中的浓度范围为 0.25 至 42.5µg/kg。在医院废水、污水处理厂出水(进水)和地表水分别检测到的这些药物的检出频率为 58%、52%(78%)和 59%。利用定量结构-活性关系模型预测,长春新碱、甲磺酸伊马替尼和他莫昔芬的预测 log K 值均高于 3,且在水中的半衰期>60d,表明其具有较高的持久性和生物累积性。基于对 9 种化合物的物种敏感性分布评估,甲壳类动物对抗癌药物最敏感。最危险的化合物是顺铂,其危害浓度为第 5 个百分位值。对于大型溞,抗癌药物主要类别的急性毒性按如下顺序排列:铂络合物>内分泌治疗剂>抗生素>抗代谢物>烷化剂。基于最低观察效应浓度(LOECs),主要使用危害商分析,环磷酰胺、顺铂、5-氟尿嘧啶、甲磺酸伊马替尼、比卡鲁胺、依托泊苷和紫杉醇对水生生物的危害最大。需要进一步研究,以确定适合风险评估阈值的慢性终点,以及更好地了解作用机制和潜在的多代毒性以及生态系统中的营养转移。