Synthesis of cationic poly(4-vinylpyridine)-functionalized colloidal particles by emulsion polymerization with reactive block copolymer for protein adsorption

J Colloid Interface Sci. 2012 Sep 1;381(1):137-42. doi: 10.1016/j.jcis.2012.05.010. Epub 2012 May 16.

Abstract

We report here a novel protein sequestration method using polymeric colloidal particles prepared by emulsion polymerization with reactive block copolymers. Specifically, poly(4-vinyl-N-ethylpyridine bromide)-block-polymethylacrylate block copolymers were synthesized from reversible addition-fragmentation chain transfer polymerization and used as emulsifiers for emulsion polymerization of poly(4-vinyl-N-ethylpyridine bromide)-functionalized polymeric colloidal particles. The particles have high and stable zeta potentials when dispersed in solution, regardless of pH variations. As a result, the polymeric colloids demonstrate a high affinity for oppositely charged proteins, even though the isoelectric points of proteins may vary greatly. We show here that BSA can be sequestered highly efficiently with a maximum binding capacity (~900 mg/g). The adsorbed protein is easily released, and the polymeric colloids are regenerated after washing with a buffer solution of high ionic strength. These properties may prompt this type of novel macromolecule-functionalized colloids to be utilized for effective protein adsorption and separation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylates / chemistry*
  • Adsorption
  • Cations
  • Colloids
  • Hydrogen-Ion Concentration
  • Isoelectric Point
  • Magnetic Resonance Spectroscopy
  • Microscopy, Electron, Transmission
  • Osmolar Concentration
  • Polyvinyls / chemistry*
  • Serum Albumin, Bovine / chemistry*
  • Solutions

Substances

  • Acrylates
  • Cations
  • Colloids
  • Polyvinyls
  • Solutions
  • poly(4-vinylpyridine)
  • Serum Albumin, Bovine