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Pharmaceuticals in water, fish and osprey nestlings in Delaware River and Bay

机译:特拉华河和湾中水,鱼和鱼鹰幼体中的药物

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Exposure of wildlife to Active Pharmaceutical Ingredients (APIs) is likely to occur but studies of risk are limited. One exposure pathway that has received attention is trophic transfer of APIs in a water-fish osprey food chain. Samples of water, fish plasma and osprey plasma were collected from Delaware River and Bay, and analyzed for 21 APIs. Only 2 of 21 analytes exceeded method detection limits in osprey plasma (acetaminophen and diclofenac) with plasma levels typically 2-3 orders of magnitude below human therapeutic concentrations (HTC). We built upon a screening level model used to predict osprey exposure to APIs in Chesapeake Bay and evaluated whether exposure levels could have been predicted in Delaware Bay had we just measured concentrations in water or fish. Use of surface water and BCFs did not predict API concentrations in fish well, likely due to fish movement patterns, and partitioning and bioaccumulation uncertainties associated with these ionizable chemicals. Input of highest measured API concentration in fish plasma combined with pharmacokinetic data accurately predicted that diclofenac and acetaminophen would be the APIs most likely detected in osprey plasma. For the majority of APIs modeled, levels were not predicted to exceed 1 ng/mL or method detection limits in osprey plasma. Based on the target analytes examined, there is little evidence that APIs represent a significant risk to ospreys nesting in Delaware Bay. If an API is present in fish orders of magnitude below HTC, sampling of fish-eating birds is unlikely to be necessary. However, several human pharmaceuticals accumulated in fish plasma within a recommended safety factor for HTC. It is now important to expand the scope of diet based API exposure modeling to include alternative exposure pathways (e.g., uptake from landfills, dumps and wastewater treatment plants) and geographic locations (developing countries) where API contamination of the environment may represent greater risk. Published by Elsevier Ltd.
机译:野生动植物可能会暴露于活性药物成分(API)中,但对风险的研究有限。一种引起关注的接触途径是水鱼鱼鹰鱼食物链中API的营养转移。从特拉华河和海湾收集水,鱼血浆和鱼鹰血浆的样品,并分析21种API。 21种分析物中只有2种超过了鱼鹰血浆(对乙酰氨基酚和双氯芬酸)的方法检测极限,血浆水平通常比人类治疗浓度(HTC)低2-3个数量级。我们建立了一个筛选水平模型,该模型用于预测切萨皮克湾的鱼油对API的鱼食暴露量,并评估了如果仅测量水或鱼中的浓度,是否可以预测特拉华湾的暴露水平。地表水和BCF的使用不能很好地预测鱼中的API浓度,这可能是由于鱼的移动方式以及与这些可离子化的化学物质相关的分配和生物累积不确定性所致。鱼血浆中最高测得的API浓度输入值与药代动力学数据相结合,可以准确地预测双氯芬酸和对乙酰氨基酚是鱼鹰血浆中极有可能检测到的API。对于大多数建模的API,预计在鱼鹰血浆中的水平不会超过1 ng / mL或方法检测极限。根据所检查的目标分析物,几乎没有证据表明API对在特拉华湾的鱼鹰筑巢构成了重大风险。如果API含量低于HTC数量级,则不太可能需要对食鱼鸟类进行采样。但是,在推荐的HTC安全系数范围内,几种人用药物在鱼血浆中积累。现在,重要的是扩大基于饮食的API暴露模型的范围,以包括替代暴露途径(例如,从垃圾填埋场,垃圾场和废水处理厂的摄取)和地理位置(发展中国家),其中API污染环境可能带来更大风险。由Elsevier Ltd.发布

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