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Self-Sterilizing, Self-Cleaning Mixed Polymeric Multifunctional Antimicrobial Surfaces.
Pappas, Harry C; Phan, Samantha; Yoon, Suhyun; Edens, Lance E; Meng, Xiangli; Schanze, Kirk S; Whitten, David G; Keller, David J.
Afiliação
  • Pappas HC; Department of Nanoscience and Microsystems Engineering, University of New Mexico , Albuquerque, New Mexico 87131-1341, United States.
  • Phan S; Center for Biomedical Engineering, Department of Chemical and Biological Engineering, University of New Mexico , Albuquerque, New Mexico 87131-1341, United States.
  • Yoon S; Department of Chemistry, University of Florida , Gainesville, Florida 32611, United States.
  • Edens LE; Department of Chemistry, University of New Mexico , Albuquerque, New Mexico 87131-1341, United States.
  • Meng X; Department of Chemistry, University of New Mexico , Albuquerque, New Mexico 87131-1341, United States.
  • Schanze KS; Department of Chemistry, University of Florida , Gainesville, Florida 32611, United States.
  • Whitten DG; Department of Chemistry, University of Florida , Gainesville, Florida 32611, United States.
  • Keller DJ; Center for Biomedical Engineering, Department of Chemical and Biological Engineering, University of New Mexico , Albuquerque, New Mexico 87131-1341, United States.
ACS Appl Mater Interfaces ; 7(50): 27632-8, 2015 Dec 23.
Article em En | MEDLINE | ID: mdl-26596644
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polímeros / Bactérias / Infecção Hospitalar / Biofilmes Limite: Humans Idioma: En Revista: ACS Appl Mater Interfaces Assunto da revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polímeros / Bactérias / Infecção Hospitalar / Biofilmes Limite: Humans Idioma: En Revista: ACS Appl Mater Interfaces Assunto da revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos