Main-Chain Polysulfonium Salts: Development of Non-Ammonium Antibacterial Polymers Similar in Their Activity to Antibiotic Drugs Vancomycin and Kanamycin

Biomacromolecules. 2021 Aug 9;22(8):3534-3542. doi: 10.1021/acs.biomac.1c00627. Epub 2021 Jul 12.

Abstract

Typically, quaternary ammonium polymers are employed for antibacterial purposes. However, a century of use has led bacteria to develop resistance to such materials. Therefore, attention is now turning toward other cationic moieties. In this context, the present work explores sulfur-based main-chain cationic polymers. The results indicate that sulfonium polymers with a β-hydroxy motif do not suffer from structural instability issues as is commonly observed in cationic polythioethers. Furthermore, they can be highly effective toward important Gram-positive bacterial strains such as Mycobacterium smegmatis, a model organism to develop drugs against rapidly spreading tuberculosis infections. More importantly, however, more challenging Gram-negative strains such as Escherichia coli can also be targeted by the polysulfoniums with equal effectiveness. Interestingly, side-chain sulfonium polyelectrolytes are observed to be devoid of any significant antibacterial activity. Finally, a comparison with kanamycin and vancomycin suggests the present polymers to be similarly effective as the bactericidal antibiotic drugs. Overall, these results indicate the effectiveness of the main-chain trivalent β-hydroxy sulfonium motif for the development of novel antibacterial polymers with a non-ammonium structure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ammonium Compounds*
  • Anti-Bacterial Agents / pharmacology
  • Kanamycin
  • Microbial Sensitivity Tests
  • Pharmaceutical Preparations*
  • Polymers
  • Salts
  • Vancomycin

Substances

  • Ammonium Compounds
  • Anti-Bacterial Agents
  • Pharmaceutical Preparations
  • Polymers
  • Salts
  • Kanamycin
  • Vancomycin