Hyperbranched poly(NIPAM) polymers modified with antibiotics for the reduction of bacterial burden in infected human tissue engineered skin

Biomaterials. 2011 Jan;32(1):258-67. doi: 10.1016/j.biomaterials.2010.08.084. Epub 2010 Oct 8.

Abstract

The escalating global incidence of bacterial infection, particularly in chronic wounds, is a problem that requires significant improvements to existing therapies. We have developed hyperbranched poly(NIPAM) polymers functionalized with the antibiotics Vancomycin and Polymyxin-B that are sensitive to the presence of bacteria in solution. Binding of bacteria to the polymers causes a conformational change, resulting in collapse of the polymers and the formation of insoluble polymer/bacteria complexes. We have applied these novel polymers to our tissue engineered human skin model of a burn wound infected with Pseudomonas aeruginosa and Staphylococcus aureus. When the polymers were removed from the infected skin, either in a polymer gel solution or in the form of hydrogel membranes, they removed bound bacteria, thus reducing the bacterial load in the infected skin model. These bacteria-binding polymers have many potential uses, including coatings for wound dressings.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylic Resins / pharmacology*
  • Anthracenes
  • Anti-Bacterial Agents / pharmacology*
  • Anti-Bacterial Agents / therapeutic use
  • Bacterial Adhesion / drug effects
  • Bacterial Infections / drug therapy
  • Bacterial Infections / microbiology*
  • Bacterial Load*
  • Humans
  • Hydrogel, Polyethylene Glycol Dimethacrylate / pharmacology
  • Membranes, Artificial
  • Microbial Sensitivity Tests
  • Models, Biological
  • Polymyxin B / pharmacology
  • Polymyxin B / therapeutic use
  • Pseudomonas Infections / drug therapy
  • Pseudomonas Infections / microbiology
  • Pseudomonas aeruginosa / cytology
  • Pseudomonas aeruginosa / drug effects
  • Skin / drug effects*
  • Skin / microbiology*
  • Skin / pathology
  • Staphylococcal Infections / drug therapy
  • Staphylococcal Infections / microbiology
  • Staphylococcus aureus / cytology
  • Staphylococcus aureus / drug effects
  • Tissue Engineering*
  • Vancomycin / pharmacology
  • Vancomycin / therapeutic use

Substances

  • Acrylic Resins
  • Anthracenes
  • Anti-Bacterial Agents
  • Membranes, Artificial
  • poly-N-isopropylacrylamide
  • Hydrogel, Polyethylene Glycol Dimethacrylate
  • Vancomycin
  • anthracene
  • Polymyxin B