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评估寄生虫病媒介传播疾病药物研发过程中的环境风险:批判性反思。

Assessing Environmental Risks during the Drug Development Process for Parasitic Vector-Borne Diseases: A Critical Reflection.

机构信息

Laboratory of Microbiology, Parasitology and Hygiene, University of Antwerp, 2610 Wilrijk, Belgium.

Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18, 08034 Barcelona, Spain.

出版信息

ACS Infect Dis. 2024 Apr 12;10(4):1026-1033. doi: 10.1021/acsinfecdis.4c00131. Epub 2024 Mar 27.

Abstract

Parasitic vector-borne diseases (VBDs) represent nearly 20% of the global burden of infectious diseases. Moreover, the spread of VBDs is enhanced by global travel, urbanization, and climate change. Treatment of VBDs faces challenges due to limitations of existing drugs, as the potential for side effects in nontarget species raises significant environmental concerns. Consequently, considering environmental risks early in drug development processes is critically important. Here, we examine the environmental risk assessment process for veterinary medicinal products in the European Union and identify major gaps in the ecotoxicity data of these drugs. By highlighting the scarcity of ecotoxicological data for commonly used antiparasitic drugs, we stress the urgent need for considering the One Health concept. We advocate for employing predictive tools and nonanimal methodologies such as New Approach Methodologies at early stages of antiparasitic drug research and development. Furthermore, adopting progressive approaches to mitigate ecological risks requires the integration of nonstandard tests that account for real-world complexities and use environmentally relevant exposure scenarios. Such a strategy is vital for a sustainable drug development process as it adheres to the principles of One Health, ultimately contributing to a healthier and more sustainable world.

摘要

寄生虫媒介传播疾病(VBDs)占全球传染病负担的近 20%。此外,全球旅行、城市化和气候变化加剧了 VBDs 的传播。由于现有药物的局限性,VBDs 的治疗面临挑战,因为这些药物在非目标物种中产生副作用的潜力引起了重大的环境关注。因此,在药物开发过程的早期考虑环境风险至关重要。在这里,我们检查了欧盟兽医药物的环境风险评估过程,并确定了这些药物的生态毒性数据中的主要差距。通过强调常用抗寄生虫药物的生态毒理学数据稀缺,我们强调迫切需要考虑“同一健康”概念。我们主张在抗寄生虫药物研究和开发的早期阶段采用预测工具和非动物方法,如新方法。此外,采用渐进的方法来减轻生态风险需要整合非标准测试,以考虑现实世界的复杂性并使用与环境相关的暴露情景。这种策略对于可持续的药物开发过程至关重要,因为它符合同一健康的原则,最终有助于一个更健康和更可持续的世界。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5892/11019539/97018449eacb/id4c00131_0001.jpg

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