Functional Silver Nanoparticle as a Benign Antimicrobial Agent That Eradicates Antibiotic-Resistant Bacteria and Promotes Wound Healing

被引:215
作者
Dai, Xiaomei [1 ]
Guo, Qianqian [1 ]
Zhao, Yu [1 ]
Zhang, Peng [2 ]
Zhang, Tianqi [1 ]
Zhang, Xinge [1 ]
Li, Chaoxing [1 ]
机构
[1] Nankai Univ, Inst Polymer Chem, Minist Educ, Key Lab Funct Polymer Mat, Tianjin 300071, Peoples R China
[2] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
silver nanoparticles; antibiotic-resistant bacteria; wound healing; nanocomposites; antibacterial mechanism; ANTIBACTERIAL PROPERTIES; GRAPHENE OXIDE; MULTIVALENT INTERACTIONS; GOLD NANOPARTICLES; EPSILON-POLYLYSINE; ESCHERICHIA-COLI; AG NANOPARTICLES; NANOFIBER; PEPTIDE; DNA;
D O I
10.1021/acsami.6b09267
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
With the increased prevalence of antibiotic-resistant bacteria infections, there is a pressed need for innovative antimicrobial agent. Here, we report a benign epsilon-polylysine/silver nanoparticle nano composite (EPL-g-butyl@AgNPs) with polyvalent and synergistic antibacterial effects. EPL-g-butyl@AgNPs exhibited good stability in aqueous solution and effective antibacterial activity against both Gram-negative (P. aeruginosa) and Gram-positive (S. aureus) bacteria without emergence of bacterial resistance. Importantly, the nanocomposites eradicated the antibiotic-resistant bacteria without toxicity to mammalian cells. Analysis of the antibacterial mechanism confirmed that the nanocomposites adhered to the bacterial surface, irreversibly disrupted the membrane structure of the bacteria, subsequently penetrated cells, and effectively inhibited protein activity, which ultimately led to bacteria apoptosis. Notably, the nanocomposites modulated the relative level of CD3(+) T cells and CD68(+) macrophages and effectively promoted infected wound healing in diabetic rats. This work improves our understanding of the antibacterial mechanism of AgNPs-based nanocomposites and offers guidance to activity prediction and rational design of effective antimicrobial nanoparticles.
引用
收藏
页码:25798 / 25807
页数:10
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