2021 Annual Meeting
(315d) Double Network Hydrogel Bioadhesives with Tunable Adhesive and Cohesive Properties
Authors
In this study, we introduce a strategy to incorporate polyelectrolyte complex (PEC) networks with GelMA to create double network (DN) hydrogels that overcome the current limitations of dilution and material loss associated with GelMA hydrogels. Mixing of oppositely charged ABA triblock polyelectrolytes and GelMA precursors results in swift formation of the PEC network comprising the oppositely charged polyelectrolytes. Block B consists of neutral polyethylene glycol (PEG), and block A is either guanidinium or sulfonate functionalized poly(allyl glycidyl ether). This self-assembled PEC network hydrogel significantly enhances the mechanical properties of GelMA precursor solution and provides a protective environment that mitigates dilution and material loss in a wet environment. Photocrosslinking of the GelMA precursors in the PEC hydrogels results in DN hydrogels that exhibit improved cohesive properties, such as superior shear moduli, Youngâs moduli, toughness, and anti-fatigue characteristics. Our DN hydrogels also exhibit remarkable improvements in adhesion with tissue surfaces as compared to GelMA hydrogels, as characterized through ex vivo burst pressure tests. Both GelMA hydrogels and DN hydrogels have higher adhesion strengths than commercial PEG-based sealant. The superior mechanical properties, biocompatibility, and biodegradability of DN hydrogel make them a promising material platform for development of robust bioadhesives.