Antibacterial multilayer films fabricated by layer-by-layer immobilizing lysozyme and gold nanoparticles on nanofibers

Colloids Surf B Biointerfaces. 2014 Apr 1:116:432-8. doi: 10.1016/j.colsurfb.2014.01.016. Epub 2014 Jan 23.

Abstract

Negatively charged gold nanoparticles (GNP) and positively charged lysozyme (Lys) were alternately deposited on negatively charged cellulose mats via layer-by-layer (LBL) self-assembly technique. The fabricated multilayer films were characterized by energy-dispersive X-ray (EDX), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectra (FT-IR), and wide-angle X-ray diffraction (XRD). Morphology of the LBL film coated mats was observed by scanning electron microscopy (SEM). Thermal degradation properties were investigated by differential scanning calorimetry (DSC) and thermo-gravimetric analysis (TGA). Additionally, the result of microbial inhibition assay indicated that the composite nanofibrous mats had excellent antibacterial activity against Escherichia coli and Staphylococcus aureus, which could be used for antimicrobial packing, tissue engineering, wound dressing, etc.

Keywords: Bacterial inhibition activity; Electrospinning; Gold nanoparticles; Layer-by-layer; Lysozyme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / metabolism
  • Anti-Bacterial Agents / pharmacology*
  • Cellulose / analogs & derivatives
  • Cellulose / chemistry
  • Cellulose / metabolism
  • Cellulose / pharmacology
  • Dose-Response Relationship, Drug
  • Escherichia coli / drug effects
  • Gold / chemistry
  • Gold / metabolism
  • Gold / pharmacology*
  • Metal Nanoparticles / chemistry*
  • Microbial Sensitivity Tests
  • Muramidase / chemistry*
  • Muramidase / metabolism
  • Nanofibers / chemistry*
  • Particle Size
  • Staphylococcus aureus / drug effects
  • Structure-Activity Relationship
  • Surface Properties

Substances

  • Anti-Bacterial Agents
  • acetylcellulose
  • Gold
  • Cellulose
  • Muramidase