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pH‐responsive destabilization and facile bioconjugation of new hydroxyl‐terminated block copolymer micelles
Authors:Behnoush Khorsand  Jung Kwon Oh
Institution:Department of Chemistry and Biochemistry, Concordia University, Montreal, Quebec, Canada H4B 1R6
Abstract:New hydroxyl‐terminated amphiphilic block copolymers (HO‐ABPs) having pendant t‐butyl groups for pH‐responsiveness and terminal OH groups for bioconjugation are reported. These HO‐ABPs consist of hydrophilic poly(oligo(ethylene oxide) monomethyl ether methacrylate) and hydrophobic poly(t‐butyl methacrylate) blocks and were synthesized by a consecutive atom transfer radical polymerization in the presence of an OH‐terminated bromine initiator. Aqueous self‐assembly of HO‐ABPs resulted in colloidally stable micellar aggregates being capable of encapsulating hydrophobic guest molecules. They were nontoxic to cells and destabilized in response to low pH. A facile bioconjugation of HO‐ABP micelles for active targeting is demonstrated by conjugation with biotin (vitamin H) and competitive assay exhibiting >93% ABP chains conjugated with biotin in each micelle. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013
Keywords:amphiphilic block copolymer  atom transfer radical polymerization (ATRP)  bioconjugation  controlled release  diblock copolymers  drug delivery systems  micelles  pH‐responsive degradation  POEMA  PtBMA
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