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Unveiling the inhibition of chlortetracycline photodegradation and the increase of toxicity when coexisting with silver nanoparticles.
Tian, Yajun; Ying, Chuhan; Zhang, Liqiu; Huang, Huimin; Song, Shuang; Mei, Rongwu; Li, Jun.
Afiliação
  • Tian Y; College of Environment, Zhejiang University of Technology, Chaowang Road 18, Hangzhou 310014, China; Beijing Key Laboratory for Source Control Technology of Water Pollution, Engineering Research Center for Water Pollution Source Control and Eco-remediation, Beijing Forestry University, Beijing 10008
  • Ying C; College of Environment, Zhejiang University of Technology, Chaowang Road 18, Hangzhou 310014, China.
  • Zhang L; Beijing Key Laboratory for Source Control Technology of Water Pollution, Engineering Research Center for Water Pollution Source Control and Eco-remediation, Beijing Forestry University, Beijing 100083, China.
  • Huang H; Zhejiang Huanke Certification Center for Environment Co., Ltd., Hangzhou 310007, China.
  • Song S; College of Environment, Zhejiang University of Technology, Chaowang Road 18, Hangzhou 310014, China.
  • Mei R; Eco-Environmental Science & Research Institute of Zhejiang Province, Hangzhou 310007, China.
  • Li J; College of Environment, Zhejiang University of Technology, Chaowang Road 18, Hangzhou 310014, China. Electronic address: tanweilijun@zjut.edu.cn.
Sci Total Environ ; 912: 168443, 2024 Feb 20.
Article em En | MEDLINE | ID: mdl-37956846
ABSTRACT
Silver nanoparticles (AgNPs) and antibiotics inevitably co-exist in water environment. Nonetheless, little is known regarding the interactions between AgNPs and antibiotics or the effects of AgNPs on environmental behavior of antibiotics, particularly on sunlight-driven transformation. In the present work, we found that AgNPs obviously inhibit the photochemical decay of chlortetracycline (CTC), and CTC boosts the dissolution of AgNPs. With the help of electron paramagnetic resonance (EPR) and quenching experiment, we ascertained that these results originated from the competition between AgNPs against CTC for capturing 1O2 generated from CTC photosensitization. 1O2 reacting with CTC contributed mostly to CTC photodegradation, while 1O2 as well reacting with AgNPs leads to release of Ag+. When compared to reaction of 1O2 with CTC, 1O2 is prone to react with AgNPs, based on lower Gibbs free energy of AgNPs reacting with 1O2. Therefore, upon CTC co-existing with AgNPs, the release of Ag+ was accelerated and the photodegradation of CTC was inhibited obviously. Furthermore, the accelerated release of Ag+ significantly increased their toxicity toward E. coli cells under simulate sunlight irradiation. Overall, the findings demonstrate how AgNPs interact with CTC and how these interactions affect the environmental behaviors of CTC or AgNPs, allowing more accurate assessments of the risk to ecosystems posed by AgNPs coexisting with antibiotics.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Clortetraciclina / Nanopartículas Metálicas Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Clortetraciclina / Nanopartículas Metálicas Idioma: En Ano de publicação: 2024 Tipo de documento: Article