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新的测试策略在授权过程中的寄生虫蜣螂。

New test strategy for dung beetles during the authorization process of parasiticides.

机构信息

Federal Environment Agency, Dessau-Rosslau, Germany.

出版信息

Integr Environ Assess Manag. 2013 Jul;9(3):524-30. doi: 10.1002/ieam.1399.

Abstract

According to European legislation, an environmental risk assessment (ERA) of veterinary medicinal products (VMPs) for dung fauna is required in the authorization process, if the substance acts as a parasiticide for the treatment of pasture animals. In the past, however, the demonstration of the environmental safety of those VMPs for dung fauna was strongly hampered by the fact that no standardized tests were available. Therefore, starting with recommendations from the Society of Environmental Toxicology and Chemistry (SETAC) advisory group, dung organism toxicity test standardization (DOTTS) test systems for phase II Tier A standardized tests on the mortality of dung fly and dung beetle larvae were developed and published by the Organisation for Economic Co-operation and Development (OECD) in 2008 and 2010. If a risk is identified for dung organisms in phase II Tier A of the ERA process, further tests are required for Tier B. So far, however, no advice is given for such studies in the existing guidelines. Therefore, 4 workshops took place between 2007 and 2009 with international dung fauna experts (Aveiro-Group) to find an appropriate test strategy for dung fauna organisms beyond Tier A mortality testing. For the first time, 2 different Tier B extended laboratory test approaches for dung beetles and test strategies for scenarios beyond Tier B are described in more detail. In case the risk assessment is still not clear, further options for Tier C (i.e., field studies) or Tier D (modeling) are briefly presented. Finally, the role of uncertainty and variability of test results is discussed, including recommendations for assessment factors for the different tiers to be used when assessing the risk of VMPs on dung organisms. The approach, especially the test strategy, will help industry, consultants, and assessors appropriately assess the environmental risk assessments during the authorization procedure of parasiticides.

摘要

根据欧洲法规,如果兽医医药产品(VMP)作为治疗牧场动物的寄生虫防治剂,则在授权过程中需要对粪便动物进行环境风险评估(ERA)。然而,在过去,由于没有标准化的测试方法,因此那些针对粪便动物的 VMP 的环境安全性的证明受到了极大的阻碍。因此,从环境毒物学和化学学会(SETAC)咨询小组的建议开始,经济合作与发展组织(OECD)于 2008 年和 2010 年制定并发布了针对粪便蝇和蜣螂幼虫死亡率的第二期 A 层标准化测试的粪便生物毒性测试标准化(DOTTS)测试系统,用于 Phase II Tier A 标准化测试。如果在 ERA 过程的第二阶段 A 层发现粪便生物存在风险,则需要进行 B 层测试。但是,到目前为止,在现有的指导方针中并没有针对这些研究的建议。因此,2007 年至 2009 年期间,国际粪便动物专家(Aveiro-Group)举行了 4 次研讨会,以寻找一种适合 A 层死亡率测试之外的粪便动物生物的测试策略。首次详细描述了针对蜣螂的 2 种不同的 B 层扩展实验室测试方法和 B 层以外的场景测试策略。如果风险评估仍然不明确,则简要介绍了 Tier C(即现场研究)或 Tier D(建模)的其他选择。最后,讨论了测试结果的不确定性和变异性的作用,包括在评估 VMP 对粪便生物的风险时用于不同层次的评估因素的建议。该方法,特别是测试策略,将有助于行业、顾问和评估人员在寄生虫防治剂的授权程序中适当评估环境风险评估。

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