Exploiting the Versatility of Polydopamine-Coated Nanoparticles to Deliver Nitric Oxide and Combat Bacterial Biofilm

Macromol Rapid Commun. 2018 Jul;39(13):e1800159. doi: 10.1002/marc.201800159. Epub 2018 May 28.

Abstract

In this study, an antimicrobial platform in the form of nitric oxide (NO) gas-releasing polydopamine (PDA)-coated iron oxide nanoparticles (IONPs) is developed for combating bacterial biofilms. NO is bound to the PDA-coated IONPs via the reaction between NO and the secondary amine moieties on PDA to form N-diazeniumdiolate (NONOate) functionality. To impart colloidal stability to the nanoparticles in aqueous solutions (e.g., phosphate buffered saline (PBS) and bacteria cell culture media M9), a polymer bearing hydrophilic and amine pendant groups, P(OEGMA)-b-P(ABA), is synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization and is subsequently grafted onto the PDA-coated IONPs by employing the Schiff base/Michael addition reaction between o-quinone and a primary amine. These nanoparticles are able to effectively disperse Pseudomonas aeruginosa biofilms (up to 79% dispersal) at submicromolar NO concentrations. In addition, the nanoparticles demonstrate excellent bactericidal activity toward P. aeruginosa planktonic and biofilm cells (up to 5-log10 reduction).

Keywords: biofilms; dopamine; functional; hybrid organic/inorganic nanoparticles; polymerization.

MeSH terms

  • Biofilms / drug effects*
  • Biofilms / growth & development
  • Coated Materials, Biocompatible* / chemistry
  • Coated Materials, Biocompatible* / pharmacology
  • Drug Carriers* / chemistry
  • Drug Carriers* / pharmacology
  • Indoles / chemistry*
  • Nanoparticles / chemistry*
  • Nitric Oxide* / chemistry
  • Nitric Oxide* / pharmacology
  • Polymers / chemistry*
  • Pseudomonas aeruginosa / physiology*

Substances

  • Coated Materials, Biocompatible
  • Drug Carriers
  • Indoles
  • Polymers
  • polydopamine
  • Nitric Oxide