Abstract
The negatively charged thermoresponsive polymers poly(benzyl methacrylate)-b-poly(acrylic acid)-b-poly(N-isopropylacrylamide) (PBzMA-b-PAAc-b-PIPAAm) were prepared by reversible-addition fragmentation chain transfer polymerization. The polymer formed core-shell polymeric micelles possessing a thermoresponsive corona composed of PAAc-b-PIPAAm below the lower critical solution temperature (LCST) of the PIPAAm chain. The nonionic thermoresponsive polymeric micelle composed of PBzMA-b-PIPAAm exhibited extensive inter-micellar aggregation after the hydrophobic phase transition of the corona-forming PIPAAm chains. In contrast, insertion of the PAAc chain into the thermoresponsive micelle maintained its dispersibility above the LCST of PIPAAm because of the electrostatic repulsion between the micelles. The micelles with short PAAc chains suppressed the effect of the negative charge derived from PAAc below the LCST because of the extended PIPAAm chain on the micellar surface. In contrast, the negative charge property appeared due to collapse of the PIPAAm layer above the LCST. This thermoresponsive change in its electrostatic behavior enables the micelle to control the adsorption and desorption of oppositely charged molecules in response to the temperature change across the LCST.
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