Permanent, non-leaching antibacterial surfaces - 2: How high density cationic surfaces kill bacterial cells

被引:593
作者
Murata, Hironobu
Koepsel, Richard R.
Matyjaszewski, Krzysztof
Russell, Alan J. [1 ]
机构
[1] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Chem & Petr Engn, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, McGowan Inst Regenerat Med, Dept Surg, Pittsburgh, PA 15219 USA
[4] Carnegie Mellon Univ, Dept Chem, Ctr Macromol Engn, Pittsburgh, PA 15213 USA
关键词
antibacterial; bacteria; polyDMAEMA; surface modification; atom transfer radical polymerization;
D O I
10.1016/j.biomaterials.2007.06.012
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Rational controlled synthesis of poly(quaternary ammonium) compounds has been used to prepare antimicrobial polymer brushes on inorganic surfaces. The systematic variation of several structural parameters of the polymeric brushes allowed us to elicit the minimum surface requirements and a probable mechanism of action for Escherichia coli cell kill. Polymeric brushes were prepared by surfaceinitiated atom transfer radical polymerization of 2-(dimethylamino)ethyl methacrylate (DMAEMA), a method that allows the molecular weight of the polymer chains to be precisely controlled as they grow from the target surface. The tertiary amino groups of the polyDMAEMA were then quaternized with alkyl bromides to provide a surface with antimicrobial activity. Dry layer thickness of the polymer brushes was controlled by polymerization time and/or initiator density on the surface. This tunability of surface structure allows the antimicrobial polymer brushes to be tailored rationally. A combinatorial screening tool was developed to elucidate the role of chain length and chain density on cell kill in a single experiment. The results indicate that surface charge density, is a critical element in designing a surface for maximum kill efficiency. The most biocidal surfaces had charge densities of greater than 1-5 x 10, 5 accessible quaternary amine units/cm(2). The relevance of this finding to the mechanism of action is discussed. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4870 / 4879
页数:10
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