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Glucose-Sensitivity of Boronic Acid Block Copolymers at Physiological pH
Debashish Roy1, Brent S Sumerlin1
1Department of Chemistry and Center for Drug Discovery, Design, and Delivery, Southern Methodist University, 3215 Daniel Avenue, Dallas, Texas 75275-0314, United States.
Abstract:
Well-defined boronic acid block copolymers were demonstrated to exhibit glucose-responsive disassembly at physiological pH. A boronic acid-containing acrylamide monomer with an electron-withdrawing substituent on the pendant phenylboronic acid moiety was polymerized by reversible addition-fragmentation chain transfer (RAFT) polymerization to yield a polymer with a boronic acid pKa = 8.2. Below this value, a block copolymer of this monomer with poly(N,N-dimethylacrylamide) self-assembled into aggregates. Addition of base to yield a pH > pKa or addition of glucose at pH = 7.4 resulted in aggregate dissociation that may prove promising for controlled delivery applications under physiological relevant conditions.

