Year: 2026
Type: article
Abstract: Acute tissue injuries demand bioadhesives with strong wet adhesion, biocompatibility, and mechanical adaptability. While mussel-inspired catechol-based adhesives hold promise, current designs often neglect the role of molecular diversity in tuning cohesion-adhesion dynamics. Inspired by the hierarchical branching of trees, where branch length and position determine fruit composition, we developed a structurally tunable bioadhesive platform by grafting five DOPA-derived catechol derivatives-varying in side-chain length and substituents-onto polyvinyl alcohol (PVA) via esterification. Computational, spectroscopic, structural, and mechanical analyses revealed that side-chain length and substituents critically modulate the adhesive and cohesive properties of the hydrogels. Among these, the PVA-CA system exhibited superior cohesion and adhesion across diverse substrates, attributed to the extended side chain and conjugated double bond of caffeic acid (CA) that enhance intramolecular packing and interfacial interactions. Ex vivo adhesion on porcine/canine cardiac, pulmonary, and intestinal tissues, along with in vivo studies in hepatic defect and skin wound models, confirmed strong adhesion, biocompatibility, and improved tissue regeneration of PVA-CA hydrogel. This work establishes a programmable molecular design strategy for next-generation wet-tissue adhesives with broad biomedical potential.
Source: Advanced Science
Language: English
Subfield: Molecular Medicine
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $6,730
Funders: Chongqing Municipal Health Commission, National Natural Science Foundation of China, Housing and Building National Research Center, Chongqing Science and Technology Commission, Natural Science Foundation of Chongqing, Yukawa Institute for Theoretical Physics, Kyoto University, Centre Scientifique et Technique du Bâtiment, Young Scientists Fund
Awards: G151148969, G4427435602, G8449424321
OpenAlex ID: W7118646383
