Journal of the American Chemical Society · 2016 · 89 citations · 21 references
Natural SciencesChemical EngineeringMaterials ScienceBiocompatibilityBiomaterialsPolymer ChemistryFree-radical PolymerizationGelsHydrogelsPolymer FunctionalizationPolymeric BiomaterialsChain-end ReactivityControlled PolymerizationControlled Radical FunctionalizationControlled Radical PolymerizationHydrophilicityMembrane HydrophilicityPolymer Chain ArchitecturePolymer Surface Modification
Zwitterionic polymers have been widely implemented in surface modification and as biomaterials that exhibit exceptional hydrophilicity, biocompatibility, and antifouling properties. However, a wider breadth of applications for polymer zwitterions is hindered by their inherent lack of functionality, requiring the integration of chain-end functionality or incorporation of functional comonomers along the polymer chain. Here we demonstrate the facile placement of unsaturated groups directly into zwitterionic methacrylate monomers, specifically choline phosphate structures, and show the utility of these monomers in controlled free radical polymerization. These versatile functional zwitterions are converted easily to polymer prodrugs, hydrogels, and other derivatives that establish the versatility of this novel materials platform.
21
Poly(2-methacryloyloxyethyl phosphorylcholine) for Protein Conjugation
Andrew L. Lewis, Yiqing Tang, Steve Brocchini et al. · Bioconjugate Chemistry · 2008 · 135 citations