A Biomimicking Non‐Swelling Wet Tissue Adhesive With Instant, Tough, and Durable Adhesion for Wound Closure

ABSTRACT Durable tough underwater tissue adhesion presents a big challenge due to the inherent materials science trade‐off between robust interfacial bonding and cohesion strength. Inspired by the synergistic adhesion mechanisms of mussel foot proteins and barnacle cement proteins, we designed and synthesized a novel adhesive via UV‐initiated copolymerization of four acrylate monomers: a long‐chain alkyl catechol derivative (Cd), its phenolic analogue (Cs), hydroxyethyl acrylate (HEA) , and dimethylaminoethyl methacrylate (DMA) . Its adhesion is water‐triggered, fast (<1 min), tough (underwater tissue adhesion strength: ∼388 kPa; interfacial toughness: ∼530 J/m 2 ), due to the strong interfacial interactions at the adhesive/adherend interface, and the good energy dissipation capacity from the high cohesive mechanical properties (stress: 724 kPa, strain: 395%, and toughness : 864 kJ/m 3 ). Moreover, its adhesion strength to underwater tissue is durable for up to 14 d, attributable to its non‐swelling properties (water adsorption ratio is just ∼4%). It can effectively close tissue incisions and facilitate wound healing. This study elucidates the influence of catechol groups, cationic moiety, and hydrophobic segments on underwater adhesion, and therefore develops a non‐swellable wet tissue adhesive for better serving the clinical needs.

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Publication Details

Journal
Advanced Healthcare Materials
Published
2026-05-28
DOI
https://doi.org/10.1002/adhm.71286
Primary Topic
Polymer Surface Interaction Studies
Type
article
Field-Weighted Citation Impact
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article

A Biomimicking Non‐Swelling Wet Tissue Adhesive With Instant, Tough, and Durable Adhesion for Wound Closure

Qinhui Chen, Peng Ni, Yunxiang Weng, Yuchen Zhang et al.
Advanced Healthcare Materials
Polymer Surface Interaction Studies
article

A Biomimicking Non‐Swelling Wet Tissue Adhesive With Instant, Tough, and Durable Adhesion for Wound Closure

Qinhui Chen, Peng Ni, Yunxiang Weng, Yuchen Zhang, Xianmou Fan, Haiqing Liu, Bingying He, Wenwen Zeng, Yan Fang, Wanting Lin
article en

Abstract

ABSTRACT Durable tough underwater tissue adhesion presents a big challenge due to the inherent materials science trade‐off between robust interfacial bonding and cohesion strength. Inspired by the synergistic adhesion mechanisms of mussel foot proteins and barnacle cement proteins, we designed and synthesized a novel adhesive via UV‐initiated copolymerization of four acrylate monomers: a long‐chain alkyl catechol derivative (Cd), its phenolic analogue (Cs), hydroxyethyl acrylate (HEA) , and dimethylaminoethyl methacrylate (DMA) . Its adhesion is water‐triggered, fast (<1 min), tough (underwater tissue adhesion strength: ∼388 kPa; interfacial toughness: ∼530 J/m 2 ), due to the strong interfacial interactions at the adhesive/adherend interface, and the good energy dissipation capacity from the high cohesive mechanical properties (stress: 724 kPa, strain: 395%, and toughness : 864 kJ/m 3 ). Moreover, its adhesion strength to underwater tissue is durable for up to 14 d, attributable to its non‐swelling properties (water adsorption ratio is just ∼4%). It can effectively close tissue incisions and facilitate wound healing. This study elucidates the influence of catechol groups, cationic moiety, and hydrophobic segments on underwater adhesion, and therefore develops a non‐swellable wet tissue adhesive for better serving the clinical needs.

Advanced Healthcare Materials
Fujian Normal University (CN), Biocatalysts (United Kingdom) (GB), Affiliated Hospital of Guangdong Medical College Hospital (CN)
National Natural Science Foundation of China, Natural Science Foundation of Fujian Province
Life below water
Openalex Percentile: Top 12%
Polymer Surface Interaction Studies
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