| Literature DB >> 26168153 |
Chitrada Kaweeteerawat1,2,3,4, Chong Hyun Chang1,2, Kevin R Roy5, Rong Liu1,2,6, Ruibin Li1,2, Daniel Toso7, Heidi Fischer8, Angela Ivask1,2,9, Zhaoxia Ji1,2, Jeffrey I Zink1,2,10, Z Hong Zhou2,11, Guillaume Francois Chanfreau5, Donatello Telesca1,2,8, Yoram Cohen1,2,6,12, Patricia Ann Holden1,13, Andre E Nel1,2,14, Hilary A Godwin1,2,3,4,6.
Abstract
Copper formulations have been used for decades for antimicrobial and antifouling applications. With the development of nanoformulations of copper that are more effective than their ionic and microsized analogues, a key regulatory question is whether these materials should be treated as new or existing materials. To address this issue, here we compare the magnitude and mechanisms of toxicity of a series of Cu species (at concentration ranging from 2 to 250 μg/mL), including nano Cu, nano CuO, nano Cu(OH)2 (CuPro and Kocide), micro Cu, micro CuO, ionic Cu(2+) (CuCl2 and CuSO4) in two species of bacteria (Escherichia coli and Lactobacillus brevis). The primary size of the particles studied ranged from 10 nm to 10 μm. Our results reveal that Cu and CuO nanoparticles (NPs) are more toxic than their microsized counterparts at the same Cu concentration, with toxicities approaching those of the ionic Cu species. Strikingly, these NPs showed distinct differences in their mode of toxicity when compared to the ionic and microsized Cu, highlighting the unique toxicity properties of materials at the nanoscale. In vitro DNA damage assays reveal that both nano Cu and microsized Cu are capable of causing complete degradation of plasmid DNA, but electron tomography results show that only nanoformulations of Cu are internalized as intact intracellular particles. These studies suggest that nano Cu at the concentration of 50 μg/mL may have unique genotoxicity in bacteria compared to ionic and microsized Cu.Entities:
Keywords: antifouling; antimicrobial; copper; ecotoxity; genotoxicity; nanoparticle; nanotoxicology
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Year: 2015 PMID: 26168153 PMCID: PMC5698005 DOI: 10.1021/acsnano.5b02021
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881