Self-Sterilizing, Self-Cleaning Mixed Polymeric Multifunctional Antimicrobial Surfaces

被引:41
|
作者
Pappas, Harry C. [1 ,2 ]
Phan, Samantha [3 ]
Yoon, Suhyun [4 ]
Edens, Lance E. [4 ]
Meng, Xiangli [3 ]
Schanze, Kirk S. [3 ]
Whitten, David G. [2 ]
Keller, David J. [4 ]
机构
[1] Univ New Mexico, Dept Nanosci & Microsyst Engn, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Dept Chem & Biol Engn, Ctr Biomed Engn, Albuquerque, NM 87131 USA
[3] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
[4] Univ New Mexico, Dept Chem, Albuquerque, NM 87131 USA
关键词
conjugated polyelectrolyte; PNIPAAm; bacteria; kill; release; AMMONIUM SILANE COATINGS; CONJUGATED POLYELECTROLYTES; ANTIBACTERIAL ACTIVITY; BIOCIDAL ACTIVITY; LIGHT; BACTERIA; LYSOZYME;
D O I
10.1021/acsami.5b06852
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Mitigation of bacterial adhesion and subsequent biofilm formation is quickly becoming a strategy for the prevention of hospital-acquired infections. We demonstrate a basic strategy for surface modification that combines the ability to control attachment by microbes with the ability to inactivate microbes. The surface consists of two active materials: poly(p-phenylene ethynylene)-based polymers, which can inactivate a wide range of microbes and pathogens, and poly(N-isopropylacrylamide)-based polymers, which can switch between an hydrophobic "capture" state and a hydrophilic "release" state. The combination of these materials creates a surface that can both bind microbes in a switchable way and kill surface-bound microbes efficiently. Considerable earlier work with cationic poly(p-phenylene ethynylene) polyelectrolytes has demonstrated and characterized their antimicrobial properties, including the ability to efficiently destroy or deactivate Gram-negative and Gram-positive bacteria, fungi, and viruses. Similarly, much work has shown (1) that surface-polymerized films of poly(N-isopropylacrylamide) are able to switch their surface thermodynamic properties from a swollen, relatively hydrophilic state at low temperature to a condensed, relatively hydrophobic state at higher temperature, and (2) that this switch can control the binding and/or release of microbes to poly(N-isopropylacrylamide) surfaces. The active surfaces described herein were fabricated by first creating a film of biocidal poly(p-phenylene ethynylene) using layer-by-layer methods, and then conferring switchable adhesion by growing poly(N-isopropylacrylamide) through the poly(p-phenylene ethynylene) layer, using surface-attached polymerization initiators. The resulting multifunctional, complex films were then characterized both physically and functionally. We demonstrate that such films kill and subsequently induce widespread release of Gram-negative and Gram-positive bacteria.
引用
收藏
页码:27632 / 27638
页数:7
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