Literature DB >> 26348846

Prioritizing human pharmaceuticals for ecological risks in the freshwater environment of Korea.

Kyunghee Ji1, Eun Jeong Han2, Sunhyoung Back3, Jeongim Park3, Jisung Ryu4, Kyungho Choi5.   

Abstract

Pharmaceutical residues are potential threats to aquatic ecosystems. Because more than 3000 active pharmaceutical ingredients (APIs) are in use, identifying high-priority pharmaceuticals is important for developing appropriate management options. Priority pharmaceuticals may vary by geographical region, because their occurrence levels can be influenced by demographic, societal, and regional characteristics. In the present study, the authors prioritized human pharmaceuticals of potential ecological risk in the Korean water environment, based on amount of use, biological activity, and regional hydrologic characteristics. For this purpose, the authors estimated the amounts of annual production of 695 human APIs in Korea. Then derived predicted environmental concentrations, using 2 approaches, to develop an initial candidate list of target pharmaceuticals. Major antineoplastic drugs and hormones were added in the initial candidate list regardless of their production amount because of their high biological activity potential. The predicted no effect concentrations were derived for those pharmaceuticals based on ecotoxicity information available in the literature or by model prediction. Priority lists of human pharmaceuticals were developed based on ecological risks and availability of relevant information. Those priority APIs identified include acetaminophen, clarithromycin, ciprofloxacin, ofloxacin, metformin, and norethisterone. Many of these pharmaceuticals have been neither adequately monitored nor assessed for risks in Korea. Further efforts are needed to improve these lists and to develop management decisions for these compounds in Korean water.
© 2015 SETAC.

Entities:  

Keywords:  Environmental risk assessment; PhATE; Pharmaceuticals; Prioritization

Mesh:

Substances:

Year:  2015        PMID: 26348846     DOI: 10.1002/etc.3233

Source DB:  PubMed          Journal:  Environ Toxicol Chem        ISSN: 0730-7268            Impact factor:   3.742


  1 in total

1.  Theoretical investigation of loratadine reactivity in order to understand its degradation properties: DFT and MD study.

Authors:  Stevan Armaković; Sanja J Armaković; Biljana F Abramović
Journal:  J Mol Model       Date:  2016-09-17       Impact factor: 1.810

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.