Facial Amphiphilicity-Induced Polymer Nanostructures for Antimicrobial Applications

ACS Appl Mater Interfaces. 2020 May 13;12(19):21221-21230. doi: 10.1021/acsami.9b19712. Epub 2020 Jan 15.

Abstract

New antimicrobial agents are needed to address ever-increasing antimicrobial resistance and a growing epidemic of infections caused by multidrug resistant pathogens. We design nanostructured antimicrobial copolymers containing multicyclic natural products that bear facial amphiphilicity. Bile acid based macromolecular architectures of these nanostructures can interact preferentially with bacterial membranes. Incorporation of polyethylene glycol into the copolymers not only improved the colloidal stability of nanostructures but also increased the biocompatibility. This study investigated the effects of facial amphiphilicity, polymer architectures, and self-assembled nanostructures on antimicrobial activity. Advanced nanostructures such as spheres, vesicles, and rod-shaped aggregates are formed in water from the facial amphiphilic cationic copolymers via supramolecular interactions. These aggregates were particularly interactive toward Gram-positive and Gram-negative bacterial cell membranes and showed low hemolysis against mammalian cells.

Keywords: antimicrobial nanostructures; bile acids; biocompatibility; charge density; facial amphiphilicity; gradient copolymers; self-assembly.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / chemical synthesis
  • Anti-Bacterial Agents / pharmacology*
  • Anti-Bacterial Agents / toxicity
  • Apoptosis / drug effects
  • Bile Acids and Salts / chemical synthesis
  • Bile Acids and Salts / pharmacology*
  • Bile Acids and Salts / toxicity
  • Erythrocytes / drug effects
  • Escherichia coli / drug effects
  • Hemolysis / drug effects
  • Mice
  • Microbial Sensitivity Tests
  • Nanostructures / chemistry
  • Nanostructures / toxicity
  • Polyethylene Glycols / chemical synthesis
  • Polyethylene Glycols / pharmacology*
  • Polyethylene Glycols / toxicity
  • Polymers / chemical synthesis
  • Polymers / pharmacology*
  • Polymers / toxicity
  • Pseudomonas aeruginosa / drug effects
  • Staphylococcus aureus / drug effects
  • Surface-Active Agents / chemical synthesis
  • Surface-Active Agents / pharmacology*
  • Surface-Active Agents / toxicity

Substances

  • Anti-Bacterial Agents
  • Bile Acids and Salts
  • Polymers
  • Surface-Active Agents
  • Polyethylene Glycols