Dual Polymerizations: Untapped Potential for Biomaterials

Application of block copolymers in medicine often relies on controlling polymer behavior by varying polymer side chains to add functionality and tune hydrophobicity. Changing the polymer backbone is an emerging powerful strategy to modulate polymer self‐assembly, rigidity, reactivity, and biodegradability. Herein, dual polymerization strategies for the synthesis of backbone‐segmented block copolymers for biomedical applications are highlighted.

Abstract

Block copolymers with unique architectures and those that can self‐assemble into supramolecular structures are used in medicine as biomaterial scaffolds and delivery vehicles for cells, therapeutics, and imaging agents. To date, much of the work relies on controlling polymer behavior by varying the monomer side chains to add functionality and tune hydrophobicity. Although varying the side chains is an efficient strategy to control polymer behavior, changing the polymer backbone can also be a powerful approach to modulate polymer self‐assembly, rigidity, reactivity, and biodegradability for biomedical applications. There are many developments in the syntheses of polymers with segmented backbones, but these developments are not widely adopted as strategies to address the unique constraints and requirements of polymers for biomedical applications. This review highlights dual polymerization strategies for the synthesis of backbone‐segmented block copolymers to facilitate their adoption for biomedical applications.

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