PH-responsive intra- and inter-molecularly micelle formation of anionic diblock copolymer in water

Abstract

Poly(sodium2-(acrylamido)-2-methylpropanesulfonate)-block-poly(sodium11-(acrylamido) undecanoate) (PAMPS-PAaU) was synthesized via reversible addition-fragmentation chain transfer (RAFT)-controlled radical polymerization. The "living" polymerization of PAaU was evidenced by the fact that the molecular weight distribution was narrow (Mw/Mn = 1.23). The pH-induced association behavior of PAMPS-PAaU in 0.1 M NaCl aqueous solutions as a function of solution pH was investigated by 1H NMR spin-spin relaxation time, dynamic light scattering (DLS), static light scattering (SLS), and fluorescence probe techniques. These results indicated that PAMPS-PAaU formed polymer micelles in 0.1 M NaCl aqueous solutions at pH < 9. At pH = 8-9, the polymer formed the micelles intramolecularly due to hydrophobic self-association of the PAaU block within the single polymer chain. On the other hand, at pH < 8, micellization occurred intermolecularly to form polymer micelles comprising hydrophobic PAaU cores and hydrophilic PAMPS shells.