Facile synthesis of rGO-MoS2-Ag nanocomposites with long-term antimicrobial activities.
Identifieur interne : 000196 ( Main/Corpus ); précédent : 000195; suivant : 000197Facile synthesis of rGO-MoS2-Ag nanocomposites with long-term antimicrobial activities.
Auteurs : Jingchen Li ; Jie Zheng ; Yadong Yu ; Zhen Su ; Lihui Zhang ; Xiaojun ChenSource :
- Nanotechnology [ 1361-6528 ] ; 2020.
English descriptors
- KwdEn :
- Anti-Bacterial Agents (chemical synthesis), Anti-Bacterial Agents (chemistry), Anti-Bacterial Agents (pharmacology), Cell Membrane (drug effects), Disulfides (chemistry), Dose-Response Relationship, Drug (MeSH), Escherichia coli (drug effects), Escherichia coli (metabolism), Graphite (chemistry), Metal Nanoparticles (MeSH), Microbial Sensitivity Tests (MeSH), Molybdenum (chemistry), Nanocomposites (chemistry), Reactive Oxygen Species (metabolism), Silver Nitrate (MeSH), Staphylococcus aureus (drug effects), Staphylococcus aureus (metabolism).
- MESH :
- chemical , chemical synthesis : Anti-Bacterial Agents.
- chemical , chemistry : Anti-Bacterial Agents, Disulfides, Graphite, Molybdenum.
- chemical , metabolism : Reactive Oxygen Species.
- chemical , pharmacology : Anti-Bacterial Agents.
- chemistry : Nanocomposites.
- drug effects : Cell Membrane, Escherichia coli, Staphylococcus aureus.
- metabolism : Escherichia coli, Staphylococcus aureus.
- Dose-Response Relationship, Drug, Metal Nanoparticles, Microbial Sensitivity Tests, Silver Nitrate.
Abstract
The abuse of antibiotics has led to the emergence of numerous super resistant bacteria, which pose a serious threat to public health. Developing nanomaterials with novel modes of bactericidal activity offers the promise of fighting pathogens without the risk of causing drug resistances. Here, we used reduced graphene oxide (rGO), bulk molybdenum disulfide (MoS2) and silver nitrate (AgNO3) to synthesize a ternary nanocomposite, rGO-MoS2-Ag, via a simple one-pot method. The resulting rGO-MoS2-Ag presented as crumpled and sheet-like structures decorated with Ag nanoparticles. The minimum inhibitory concentration and minimum bactericidal concentration of rGO-MoS2-Ag against Escherichia coli were 50 and 100 μg ml-1, while Staphylococcus aureus reacted only to twice higher concentrations of 100 and 200 μg ml-1, respectively. Notably, rGO-MoS2-Ag exhibited better antibacterial activity towards E. coli and S. aureus than rGO, MoS2, or rGO-MoS2. This result can be attributed to the excellent performance of rGO-MoS2-Ag in destroying the bacterial cell membrane and inducing the generation of reactive oxygen species. The Ag+ ion release of rGO-MoS2-Ag was delayed, endowing the nanocomposite with long-term antibacterial capabilities and better biosafety. Our results indicate that the as-prepared rGO-MoS2-Ag has promising potential for application in biomedicine and public health.
DOI: 10.1088/1361-6528/ab5ba7
PubMed: 31770730
Links to Exploration step
pubmed:31770730Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Facile synthesis of rGO-MoS<sub>2</sub>
-Ag nanocomposites with long-term antimicrobial activities.</title>
<author><name sortKey="Li, Jingchen" sort="Li, Jingchen" uniqKey="Li J" first="Jingchen" last="Li">Jingchen Li</name>
<affiliation><nlm:affiliation>College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, People's Republic of China.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Zheng, Jie" sort="Zheng, Jie" uniqKey="Zheng J" first="Jie" last="Zheng">Jie Zheng</name>
</author>
<author><name sortKey="Yu, Yadong" sort="Yu, Yadong" uniqKey="Yu Y" first="Yadong" last="Yu">Yadong Yu</name>
</author>
<author><name sortKey="Su, Zhen" sort="Su, Zhen" uniqKey="Su Z" first="Zhen" last="Su">Zhen Su</name>
</author>
<author><name sortKey="Zhang, Lihui" sort="Zhang, Lihui" uniqKey="Zhang L" first="Lihui" last="Zhang">Lihui Zhang</name>
</author>
<author><name sortKey="Chen, Xiaojun" sort="Chen, Xiaojun" uniqKey="Chen X" first="Xiaojun" last="Chen">Xiaojun Chen</name>
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-Ag nanocomposites with long-term antimicrobial activities.</title>
<author><name sortKey="Li, Jingchen" sort="Li, Jingchen" uniqKey="Li J" first="Jingchen" last="Li">Jingchen Li</name>
<affiliation><nlm:affiliation>College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, People's Republic of China.</nlm:affiliation>
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<author><name sortKey="Zheng, Jie" sort="Zheng, Jie" uniqKey="Zheng J" first="Jie" last="Zheng">Jie Zheng</name>
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<author><name sortKey="Yu, Yadong" sort="Yu, Yadong" uniqKey="Yu Y" first="Yadong" last="Yu">Yadong Yu</name>
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<author><name sortKey="Su, Zhen" sort="Su, Zhen" uniqKey="Su Z" first="Zhen" last="Su">Zhen Su</name>
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<author><name sortKey="Zhang, Lihui" sort="Zhang, Lihui" uniqKey="Zhang L" first="Lihui" last="Zhang">Lihui Zhang</name>
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<author><name sortKey="Chen, Xiaojun" sort="Chen, Xiaojun" uniqKey="Chen X" first="Xiaojun" last="Chen">Xiaojun Chen</name>
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<series><title level="j">Nanotechnology</title>
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<term>Anti-Bacterial Agents (chemistry)</term>
<term>Anti-Bacterial Agents (pharmacology)</term>
<term>Cell Membrane (drug effects)</term>
<term>Disulfides (chemistry)</term>
<term>Dose-Response Relationship, Drug (MeSH)</term>
<term>Escherichia coli (drug effects)</term>
<term>Escherichia coli (metabolism)</term>
<term>Graphite (chemistry)</term>
<term>Metal Nanoparticles (MeSH)</term>
<term>Microbial Sensitivity Tests (MeSH)</term>
<term>Molybdenum (chemistry)</term>
<term>Nanocomposites (chemistry)</term>
<term>Reactive Oxygen Species (metabolism)</term>
<term>Silver Nitrate (MeSH)</term>
<term>Staphylococcus aureus (drug effects)</term>
<term>Staphylococcus aureus (metabolism)</term>
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<keywords scheme="MESH" type="chemical" qualifier="chemical synthesis" xml:lang="en"><term>Anti-Bacterial Agents</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Anti-Bacterial Agents</term>
<term>Disulfides</term>
<term>Graphite</term>
<term>Molybdenum</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Reactive Oxygen Species</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Anti-Bacterial Agents</term>
</keywords>
<keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Nanocomposites</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Cell Membrane</term>
<term>Escherichia coli</term>
<term>Staphylococcus aureus</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Escherichia coli</term>
<term>Staphylococcus aureus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Dose-Response Relationship, Drug</term>
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<front><div type="abstract" xml:lang="en">The abuse of antibiotics has led to the emergence of numerous super resistant bacteria, which pose a serious threat to public health. Developing nanomaterials with novel modes of bactericidal activity offers the promise of fighting pathogens without the risk of causing drug resistances. Here, we used reduced graphene oxide (rGO), bulk molybdenum disulfide (MoS<sub>2</sub>
) and silver nitrate (AgNO<sub>3</sub>
) to synthesize a ternary nanocomposite, rGO-MoS<sub>2</sub>
-Ag, via a simple one-pot method. The resulting rGO-MoS<sub>2</sub>
-Ag presented as crumpled and sheet-like structures decorated with Ag nanoparticles. The minimum inhibitory concentration and minimum bactericidal concentration of rGO-MoS<sub>2</sub>
-Ag against Escherichia coli were 50 and 100 μg ml<sup>-1</sup>
, while Staphylococcus aureus reacted only to twice higher concentrations of 100 and 200 μg ml<sup>-1</sup>
, respectively. Notably, rGO-MoS<sub>2</sub>
-Ag exhibited better antibacterial activity towards E. coli and S. aureus than rGO, MoS<sub>2</sub>
, or rGO-MoS<sub>2</sub>
. This result can be attributed to the excellent performance of rGO-MoS<sub>2</sub>
-Ag in destroying the bacterial cell membrane and inducing the generation of reactive oxygen species. The Ag<sup>+</sup>
ion release of rGO-MoS<sub>2</sub>
-Ag was delayed, endowing the nanocomposite with long-term antibacterial capabilities and better biosafety. Our results indicate that the as-prepared rGO-MoS<sub>2</sub>
-Ag has promising potential for application in biomedicine and public health.</div>
</front>
</TEI>
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<DateCompleted><Year>2020</Year>
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<ArticleTitle>Facile synthesis of rGO-MoS<sub>2</sub>
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<Abstract><AbstractText>The abuse of antibiotics has led to the emergence of numerous super resistant bacteria, which pose a serious threat to public health. Developing nanomaterials with novel modes of bactericidal activity offers the promise of fighting pathogens without the risk of causing drug resistances. Here, we used reduced graphene oxide (rGO), bulk molybdenum disulfide (MoS<sub>2</sub>
) and silver nitrate (AgNO<sub>3</sub>
) to synthesize a ternary nanocomposite, rGO-MoS<sub>2</sub>
-Ag, via a simple one-pot method. The resulting rGO-MoS<sub>2</sub>
-Ag presented as crumpled and sheet-like structures decorated with Ag nanoparticles. The minimum inhibitory concentration and minimum bactericidal concentration of rGO-MoS<sub>2</sub>
-Ag against Escherichia coli were 50 and 100 μg ml<sup>-1</sup>
, while Staphylococcus aureus reacted only to twice higher concentrations of 100 and 200 μg ml<sup>-1</sup>
, respectively. Notably, rGO-MoS<sub>2</sub>
-Ag exhibited better antibacterial activity towards E. coli and S. aureus than rGO, MoS<sub>2</sub>
, or rGO-MoS<sub>2</sub>
. This result can be attributed to the excellent performance of rGO-MoS<sub>2</sub>
-Ag in destroying the bacterial cell membrane and inducing the generation of reactive oxygen species. The Ag<sup>+</sup>
ion release of rGO-MoS<sub>2</sub>
-Ag was delayed, endowing the nanocomposite with long-term antibacterial capabilities and better biosafety. Our results indicate that the as-prepared rGO-MoS<sub>2</sub>
-Ag has promising potential for application in biomedicine and public health.</AbstractText>
</Abstract>
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