Silver nanoparticles decorated lipase-sensitive polyurethane micelles for on-demand release of silver nanoparticles

被引:43
作者
Su, Yu-Ling [1 ]
Zhao, Lili [1 ]
Meng, Fancui [1 ]
Wang, Quanxin [1 ]
Yao, Yongchao [1 ]
Luo, Jianbin [1 ]
机构
[1] Southwest Univ Nationalities, Coll Chem & Environm Protect Engn, Chengdu 610041, Peoples R China
关键词
Silver nanoparticles; Lipase sensitive; Polyurethane micelles; Antibacterial; Biocompatible; EXCELLENT ANTIBACTERIAL EFFICACY; IN-VITRO; BIOMEDICAL APPLICATIONS; HEMOLYTIC-ACTIVITY; POLYMER VESICLES; DRUG-DELIVERY; CELLS; SIZE; CYTOTOXICITY; BACTERIA;
D O I
10.1016/j.colsurfb.2017.01.036
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In order to improve the antibacterial activities while decrease the cytotoxity of silver nanoparticles, we prepared a novel nanocomposites composed of silver nanoparticles decorated lipase-sensitive polyurethane micelles (PUM-Ag) with MPEG brush on the surface. The nanocomposite was characterized by UV-vis, TEM and DLS. UV-vis and TEM demonstrated the formation of silver nanoparticles on PU micelles and the nanoassembly remained intact without the presence of lipase. The silver nanoparticles were protected by the polymer matrix and PEG brush which show good cytocompatibility to HUVEC cells and low hemolysis. Moreover, at the presence of lipase, the polymer matrix of nanocomposites is subject to degradation and the small silver nanoparticles were released as is shown by DLS and TEM. The MIC and MBC studies showed an enhanced toxicity of the nanocomposites to both gram negative and gram positive bacteria, i.e. E. coli and S. aureus, as the result of the degradation of polymer matrix by bacterial lipase. Therefore, the nanocomposites are biocompatible to mammalian cells cells which can also lead to activated smaller silver nanoparticles release at the presence of bacteria and subsequently enhanced inhibition of bacteria growth. The satisfactory selectivity for bacteria compared to HUVEC and RBCs make PUM-Ag a promising antibacterial nanomedicine in biomedical field. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:238 / 244
页数:7
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