4.7 Article

Nano-cell and nano-pollutant interactions constitute key elements in nanoparticle-pollutant combined cytotoxicity

期刊

JOURNAL OF HAZARDOUS MATERIALS
卷 418, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.jhazmat.2021.126259

关键词

Carbon nanoparticles; Zinc oxide nanoparticles; Combined cytotoxicity; Nano-cell interaction; Nano-pollutant interaction

资金

  1. National Natural Science Foundation of China [91743107, 22076033, 22036002]
  2. National Key R&D Program of China [2016YFA0203103]
  3. Pearl River Talent Recruitment Pro-gram of Guangdong Province [2019ZT08L387]

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The interaction between nano-cell and nano-pollutant plays a crucial role in determining the combined cytotoxicity of nanoparticles and pollutants. The impact of CNPs and ZnONPs on Cr(VI) differs, with CNPs reducing the cytotoxicity of CNP-Cr(VI) adducts while ZnONPs enhancing the cytotoxicity of ZnONP-Cr(VI) adducts. In-depth investigations on the interaction mechanisms are essential for a comprehensive understanding of the combined cytotoxicity of different NPs and pollutants.
As the wide application of carbon nanoparticles (CNPs) and zinc oxide nanoparticles (ZnONPs), as well as ubiquitous chromium (Cr(VI)) pollution in environment, the chance of human exposure to CNPs/ZnONPs and their Cr(VI) adducts is enhanced. We therefore investigated the impacts of nano-cell and nano-Cr(VI) interactions on nanoparticle-Cr(VI) combined cytotoxicity in human lung epithelial (A549) cells. Our results showed that nano-cell and nano-pollutant interactions were the key elements in NP-pollutant combined cytotoxicity, as determined by cell death, oxidative stress and mitochondrial dysfunction. A strong adsorption of Cr(VI) on CNPs and reduction of Cr(VI) to Cr(III) were confirmed, resulting in the reduced cytotoxicity of CNP-Cr(VI) adducts. In contrast, ZnONPs caused the destruction of cell membranes so that more ZnONP-Cr(VI) adducts could enter the cells. Meantime, more Cr contents could be released from ZnONP-Cr(VI) adducts once entering cells and locating in lysosomes than that from CNP-Cr(VI) adducts. These two reasons together caused the enhanced cytotoxicity of ZnONP-Cr(VI) adducts. These findings indicate that the in-depth investigations on the interaction mechanisms are crucial to comprehensively understand the combined cytotoxicity of different NPs and pollutants.

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