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N-Acetyl Cysteine-Decorated Nitric Oxide-Releasing Interface for Biomedical Applications.
Pandey, Rashmi; Pinon, Vicente; Garren, Mark; Maffe, Patrick; Mondal, Arnab; Brisbois, Elizabeth J; Handa, Hitesh.
Afiliação
  • Pandey R; School of Chemical, Materials, and Biomedical Engineering, College of Engineering, University of Georgia, Athens, Georgia 30602, United States.
  • Pinon V; Pharmaceutical and Biomedical Science Department, College of Pharmacy, University of Georgia, Athens, Georgia 30602, United States.
  • Garren M; School of Chemical, Materials, and Biomedical Engineering, College of Engineering, University of Georgia, Athens, Georgia 30602, United States.
  • Maffe P; School of Chemical, Materials, and Biomedical Engineering, College of Engineering, University of Georgia, Athens, Georgia 30602, United States.
  • Mondal A; School of Chemical, Materials, and Biomedical Engineering, College of Engineering, University of Georgia, Athens, Georgia 30602, United States.
  • Brisbois EJ; School of Chemical, Materials, and Biomedical Engineering, College of Engineering, University of Georgia, Athens, Georgia 30602, United States.
  • Handa H; School of Chemical, Materials, and Biomedical Engineering, College of Engineering, University of Georgia, Athens, Georgia 30602, United States.
ACS Appl Mater Interfaces ; 16(19): 24248-24260, 2024 May 15.
Article em En | MEDLINE | ID: mdl-38693878
ABSTRACT
Biomedical devices are vulnerable to infections and biofilm formation, leading to extended hospital stays, high expenditure, and increased mortality. Infections are clinically treated via the administration of systemic antibiotics, leading to the development of antibiotic resistance. A multimechanistic strategy is needed to design an effective biomaterial with broad-spectrum antibacterial potential. Recent approaches have investigated the fabrication of innately antimicrobial biomedical device surfaces in the hope of making the antibiotic treatment obsolete. Herein, we report a novel fabrication strategy combining antibacterial nitric oxide (NO) with an antibiofilm agent N-acetyl cysteine (NAC) on a polyvinyl chloride surface using polycationic polyethylenimine (PEI) as a linker. The designed biomaterial could release NO for at least 7 days with minimal NO donor leaching under physiological conditions. The proposed surface technology significantly reduced the viability of Gram-negative Escherichia coli (>97%) and Gram-positive Staphylococcus aureus (>99%) bacteria in both adhered and planktonic forms in a 24 h antibacterial assay. The composites also exhibited a significant reduction in biomass and extra polymeric substance accumulation in a dynamic environment over 72 h. Overall, these results indicate that the proposed combination of the NO donor with mucolytic NAC on a polymer surface efficiently resists microbial adhesion and can be used to prevent device-associated biofilm formation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Acetilcisteína / Staphylococcus aureus / Biofilmes / Escherichia coli / Antibacterianos / Óxido Nítrico Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Acetilcisteína / Staphylococcus aureus / Biofilmes / Escherichia coli / Antibacterianos / Óxido Nítrico Idioma: En Ano de publicação: 2024 Tipo de documento: Article