Abstract
ABSTRACTA pH-triggered drug release system of poly(ethylene oxide)-b-poly(glycidyl methacrylate) (PEO-b-PGMA) micelles was described. The PEO-b-PGMA block copolymers were synthesized by the reversible addition-fragmentation chain transfer (RAFT) polymerization of GMA with the PEO-macroinitiator. Subsequently, the hydroxyl groups were introduced to the block copolymer by epoxide ring-opening reaction of PGMA parts. The hydrophobic anticancer drug, doxorubicin (DOX), was conjugated to the polymer by acid cleavable hydrazone bonds, resulting in a pH-responsive controlled release system. The block copolymer and core-shell structure of DOX bearing PEO-b-PGMA were characterized by using FT-IR, 1H NMR, and TEM analyses. The pH-triggered release of DOX from the micellar core was investigated at pH 5.0 and 7.4, indicating a controlled drug delivery characteristic.
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