Surface functionality as a means to impact polymer nanoparticle size and structure

Langmuir. 2013 Mar 26;29(12):4092-5. doi: 10.1021/la304075c. Epub 2013 Mar 11.

Abstract

When polymeric nanoparticles (NPs) are formed by nanoprecipitation, which is a nucleation-growth process, the control over size requires changing the polymer concentration or solvent composition. Here, we demonstrate that the NP size can be controlled independent of polymer variables by introducing a polyelectrolyte (PE) in the aqueous phase. PEs that exhibit hydrogen bonding (H-bonding) yield a reduction in NP size, whereas PEs that do not possess this characteristic promote the formation of larger NPs. The observed effect can be attributed to the formation of a diffusional barrier around the NP in the form of a dense shell. This principle of controlling NP size is not limited to polymers and can also be employed in the production of lipid NPs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylic Resins / chemistry*
  • Diffusion
  • Hydrogen Bonding
  • Lactic Acid / chemistry*
  • Microscopy, Electron, Transmission
  • Nanoparticles / chemistry*
  • Nanoparticles / ultrastructure
  • Particle Size
  • Polyesters / chemistry
  • Polyglycolic Acid / chemistry*
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Polystyrenes / chemistry*
  • Solvents / chemistry
  • Surface Properties
  • Water / chemistry

Substances

  • Acrylic Resins
  • Polyesters
  • Polystyrenes
  • Solvents
  • Water
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • polycaprolactone
  • Polyglycolic Acid
  • Lactic Acid
  • carbopol 940
  • polystyrene sulfonic acid