Atomic-engineered gold@silvergold alloy nanoflowers for in vivo inhibition of bacteria

被引:20
作者
Yan, Wenjing [1 ]
Yang, Longping [1 ]
Wang, Hongxia [1 ]
Zhang, Jianhao [1 ]
Shen, Wenbiao [2 ]
机构
[1] Nanjing Agr Univ, Coll Food Sci & Technol, Natl Ctr Meat Qual & Safety Control, Nanjing 210095, Jiangsu, Peoples R China
[2] Nanjing Agr Univ, Coll Life Sci, Nanjing 210095, Jiangsu, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
ENHANCED ANTIBACTERIAL ACTIVITY; MAGNETIC NANOPARTICLES; ANTIMICROBIAL ACTIVITY; MOLECULAR-MECHANISM; SHELL; NANOSTRUCTURES; ASSEMBLIES; PYRAMIDS; NANORODS; ADHESION;
D O I
10.1039/c8nr04196b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The problems of multidrug-resistant bacteria and environmental pollution associated with the abuse of antibiotics call for effective antibiotic alternatives. Here, gold@silvergold alloy nanoflowers (Au@AgAu ANFs) with distinct atomic structures are first fabricated and then demonstrated for in vivo inhibition of bacteria. The Au@AgAu ANFs display high antibacterial activity against the model Gram-negative bacterium Escherichia coli, with a minimum inhibitory concentration value of 4.8 g mL(-1), which is 3.1 times lower than that of silver nanoparticles. The alloy structure with a rough surface enables Au@AgAu ANFs to firmly adhere to the bacterial surface and damage the cell membrane, resulting in long-term (48 h) and highly stable (30 days) antibacterial activity. Meanwhile, the Au@AgAu ANFs show remarkable biocompatibility with human cells even at a high concentration of 40 g mL(-1). Application of Au@AgAu ANFs in the treatment of bacterial infections in the mouse intestine significantly reduces the reproduction of bacteria compared to an untreated mouse, giving results similar to those of the current antibiotic treatment, with no cytotoxicity. Our study opens up a new avenue for the rational design of safe and highly efficient antibacterial materials.
引用
收藏
页码:15661 / 15668
页数:8
相关论文
共 51 条
[1]   Nanotoxicity of cobalt induced by oxidant generation and glutathione depletion in MCF-7 cells [J].
Akhtar, Mohd Javed ;
Ahamed, Maqusood ;
Alhadlaq, Hisham A. ;
Alshamsan, Aws .
TOXICOLOGY IN VITRO, 2017, 40 :94-101
[2]   Cytotoxicity and Genotoxicity of Silver Nanoparticles in Human Cells [J].
AshaRani, P. V. ;
Mun, Grace Low Kah ;
Hande, Manoor Prakash ;
Valiyaveettil, Suresh .
ACS NANO, 2009, 3 (02) :279-290
[3]   Enhanced antibacterial activity of bimetallic gold-silver core-shell nanoparticles at low silver concentration [J].
Banerjee, Madhuchanda ;
Sharma, Shilpa ;
Chattopadhyay, Arun ;
Ghosh, Siddhartha Sankar .
NANOSCALE, 2011, 3 (12) :5120-5125
[4]   Visible-light-driven enhanced antibacterial and biofilm elimination activity of graphitic carbon nitride by embedded Ag nanoparticles [J].
Bing, Wei ;
Chen, Zhaowei ;
Sun, Hanjun ;
Shi, Peng ;
Gao, Nao ;
Ren, Jinsong ;
Qu, Xiaogang .
NANO RESEARCH, 2015, 8 (05) :1648-1658
[5]  
Cagno V, 2018, NAT MATER, V17, P195, DOI [10.1038/nmat5053, 10.1038/NMAT5053]
[6]   Shape-Dependent Biomimetic Inhibition of Enzyme by Nanoparticles and Their Antibacterial Activity [J].
Cha, Sang-Ho ;
Hong, Jin ;
McGuffie, Matt ;
Yeom, Bongjun ;
VanEpps, J. Scott ;
Kotov, Nicholas A. .
ACS NANO, 2015, 9 (09) :9097-9105
[7]   General synthesis of silica-based yolk/shell hybrid nanomaterials and in vivo tumor vasculature targeting [J].
Chen, Feng ;
Goel, Shreya ;
Shi, Sixiang ;
Barnhart, Todd E. ;
Lan, Xiaoli ;
Cai, Weibo .
NANO RESEARCH, 2018, 11 (09) :4890-4904
[8]   Silver as Antibacterial Agent: Ion, Nanoparticle, and Metal [J].
Chernousova, Svitlana ;
Epple, Matthias .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (06) :1636-1653
[9]   Enhanced Antibacterial Activity of Bifunctional Fe3O4-Ag Core-Shell Nanostructures [J].
Chudasama, Bhupendra ;
Vala, Anjana K. ;
Andhariya, Nidhi ;
Upadhyay, R. V. ;
Mehta, R. V. .
NANO RESEARCH, 2009, 2 (12) :955-965
[10]   The molecular mechanism of action of bactericidal gold nanoparticles on Escherichia coli [J].
Cui, Yan ;
Zhao, Yuyun ;
Tian, Yue ;
Zhang, Wei ;
Lu, Xiaoying ;
Jiang, Xingyu .
BIOMATERIALS, 2012, 33 (07) :2327-2333