Morphology-dependent bactericidal activities of Ag/CeO2 catalysts against Escherichia coli.
Identifieur interne : 000858 ( Main/Corpus ); précédent : 000857; suivant : 000859Morphology-dependent bactericidal activities of Ag/CeO2 catalysts against Escherichia coli.
Auteurs : Lian Wang ; Hong He ; Yunbo Yu ; Li Sun ; Sijin Liu ; Changbin Zhang ; Lian HeSource :
- Journal of inorganic biochemistry [ 1873-3344 ] ; 2014.
English descriptors
- KwdEn :
- Anti-Bacterial Agents (chemistry), Anti-Bacterial Agents (pharmacology), Catalysis (MeSH), Cell Membrane (drug effects), Cell Membrane (ultrastructure), Cell Wall (drug effects), Cell Wall (ultrastructure), Cerium (chemistry), Cerium (pharmacology), Escherichia coli (cytology), Escherichia coli (drug effects), Escherichia coli (metabolism), Microbial Sensitivity Tests (MeSH), Microbial Viability (MeSH), Nanoparticles (chemistry), Oxides (chemistry), Oxides (pharmacology), Particle Size (MeSH), Reactive Oxygen Species (metabolism), Silver Compounds (chemistry), Silver Compounds (pharmacology).
- MESH :
- chemical , chemistry : Anti-Bacterial Agents, Cerium, Oxides, Silver Compounds.
- chemical , metabolism : Reactive Oxygen Species.
- chemical , pharmacology : Anti-Bacterial Agents, Cerium, Oxides, Silver Compounds.
- chemistry : Nanoparticles.
- cytology : Escherichia coli.
- drug effects : Cell Membrane, Cell Wall, Escherichia coli.
- metabolism : Escherichia coli.
- ultrastructure : Cell Membrane, Cell Wall.
- Catalysis, Microbial Sensitivity Tests, Microbial Viability, Particle Size.
Abstract
Silver-loaded CeO2 nanomaterials (Ag/CeO2) including Ag/CeO2 nanorods, nanocubes, nanoparticles were prepared with hydrothermal and impregnation methods. Catalytic inactivation of Escherichia coli with Ag/CeO2 catalysts through the formation of reactive oxygen species (ROS) was investigated. For comparison purposes, the bactericidal activities of CeO2 nanorods, nanocubes and nanoparticles were also studied. There was a 3-4 log order improvement in the inactivation of E. coli with Ag/CeO2 catalysts compared with CeO2 catalysts. Temperature-programmed reduction of H2 showed that Ag/CeO2 catalysts had higher catalytic oxidation ability than CeO2 catalysts, which was the reason for that Ag/CeO2 catalysts exhibited stronger bactericidal activities than CeO2 catalysts. Further, the bactericidal activities of CeO2 and Ag/CeO2 depend on their shapes. Results of 5,5-dimethyl-1-pyrroline-N-oxide spin-trapping measurements by electron spin resonance and addition of catalase as a scavenger indicated the formation of OH, O2(-), and H2O2, which caused the obvious bactericidal activity of catalysts. The stronger chemical bond between Ag and CeO2 nanorods led to lower Ag(+) elution concentrations. The toxicity of Ag(+) eluted from the catalysts did not play an important role during the bactericidal process. Experimental results also indicated that Ag/CeO2 induced the production of intracellular ROS and disruption of the cell wall and cell membrane. A possible production mechanism of ROS and bactericidal mechanism of catalytic oxidation were proposed.
DOI: 10.1016/j.jinorgbio.2014.02.016
PubMed: 24662462
Links to Exploration step
pubmed:24662462Le document en format XML
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<term>Cell Membrane (ultrastructure)</term>
<term>Cell Wall (drug effects)</term>
<term>Cell Wall (ultrastructure)</term>
<term>Cerium (chemistry)</term>
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<term>Escherichia coli (cytology)</term>
<term>Escherichia coli (drug effects)</term>
<term>Escherichia coli (metabolism)</term>
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<term>Microbial Viability (MeSH)</term>
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<term>Oxides (chemistry)</term>
<term>Oxides (pharmacology)</term>
<term>Particle Size (MeSH)</term>
<term>Reactive Oxygen Species (metabolism)</term>
<term>Silver Compounds (chemistry)</term>
<term>Silver Compounds (pharmacology)</term>
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<front><div type="abstract" xml:lang="en">Silver-loaded CeO2 nanomaterials (Ag/CeO2) including Ag/CeO2 nanorods, nanocubes, nanoparticles were prepared with hydrothermal and impregnation methods. Catalytic inactivation of Escherichia coli with Ag/CeO2 catalysts through the formation of reactive oxygen species (ROS) was investigated. For comparison purposes, the bactericidal activities of CeO2 nanorods, nanocubes and nanoparticles were also studied. There was a 3-4 log order improvement in the inactivation of E. coli with Ag/CeO2 catalysts compared with CeO2 catalysts. Temperature-programmed reduction of H2 showed that Ag/CeO2 catalysts had higher catalytic oxidation ability than CeO2 catalysts, which was the reason for that Ag/CeO2 catalysts exhibited stronger bactericidal activities than CeO2 catalysts. Further, the bactericidal activities of CeO2 and Ag/CeO2 depend on their shapes. Results of 5,5-dimethyl-1-pyrroline-N-oxide spin-trapping measurements by electron spin resonance and addition of catalase as a scavenger indicated the formation of OH, O2(-), and H2O2, which caused the obvious bactericidal activity of catalysts. The stronger chemical bond between Ag and CeO2 nanorods led to lower Ag(+) elution concentrations. The toxicity of Ag(+) eluted from the catalysts did not play an important role during the bactericidal process. Experimental results also indicated that Ag/CeO2 induced the production of intracellular ROS and disruption of the cell wall and cell membrane. A possible production mechanism of ROS and bactericidal mechanism of catalytic oxidation were proposed. </div>
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<Abstract><AbstractText>Silver-loaded CeO2 nanomaterials (Ag/CeO2) including Ag/CeO2 nanorods, nanocubes, nanoparticles were prepared with hydrothermal and impregnation methods. Catalytic inactivation of Escherichia coli with Ag/CeO2 catalysts through the formation of reactive oxygen species (ROS) was investigated. For comparison purposes, the bactericidal activities of CeO2 nanorods, nanocubes and nanoparticles were also studied. There was a 3-4 log order improvement in the inactivation of E. coli with Ag/CeO2 catalysts compared with CeO2 catalysts. Temperature-programmed reduction of H2 showed that Ag/CeO2 catalysts had higher catalytic oxidation ability than CeO2 catalysts, which was the reason for that Ag/CeO2 catalysts exhibited stronger bactericidal activities than CeO2 catalysts. Further, the bactericidal activities of CeO2 and Ag/CeO2 depend on their shapes. Results of 5,5-dimethyl-1-pyrroline-N-oxide spin-trapping measurements by electron spin resonance and addition of catalase as a scavenger indicated the formation of OH, O2(-), and H2O2, which caused the obvious bactericidal activity of catalysts. The stronger chemical bond between Ag and CeO2 nanorods led to lower Ag(+) elution concentrations. The toxicity of Ag(+) eluted from the catalysts did not play an important role during the bactericidal process. Experimental results also indicated that Ag/CeO2 induced the production of intracellular ROS and disruption of the cell wall and cell membrane. A possible production mechanism of ROS and bactericidal mechanism of catalytic oxidation were proposed. </AbstractText>
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