Amphiphilic polybetaines: the effect of side-chain hydrophobicity on protein adsorption

Biomacromolecules. 2012 May 14;13(5):1233-9. doi: 10.1021/bm201791p. Epub 2012 Apr 19.

Abstract

Novel amphiphilic polybetaines were synthesized and used as the base material for nonfouling coatings. The amphiphilicity of these polybetaines was systematically tuned by coupling chains of increasing hydrophobicity to the zwitterionic functionality side at the repeat unit level. An oligoethylene glycol (OEG) moiety was selected to yield the most hydrophilic coating, while octyl (C(8)) and fluorinated (F) groups were used to impart lipophilicity and lipophobicity to the coatings, respectively. This unique design allowed us to investigate the effect of the lipophilicity/lipophobicity of the side chain on the nonfouling properties of these zwitterionic systems. Adsorption studies, performed using six different proteins, showed that the fluorinated polybetaine, Poly[NFZI-co-NSi], resisted nonspecific adsorption as effectively as, and in some cases even better than, the most hydrophilic Poly[NOEGZI-co-NSi] coating. The comparison of Poly[NFZI-co-NSi] to its noncharged analog demonstrated the essential nature of the zwitterionic functionality in imparting nonfouling character to the coating.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adsorption
  • Hydrophobic and Hydrophilic Interactions
  • Molecular Structure
  • Organosilicon Compounds / chemical synthesis
  • Organosilicon Compounds / chemistry*
  • Particle Size
  • Polymers / chemical synthesis
  • Polymers / chemistry*
  • Proteins / chemistry*
  • Quaternary Ammonium Compounds / chemical synthesis
  • Quaternary Ammonium Compounds / chemistry*
  • Surface Properties
  • Surface-Active Agents / pharmacology*

Substances

  • Organosilicon Compounds
  • Polymers
  • Proteins
  • Quaternary Ammonium Compounds
  • Surface-Active Agents