Hypothesis / aims of study
Postoperative anastomotic complications, such as urinary leakage, remain a critical challenge in bladder enlargement surgery due to tension-induced tissue damage during urine storage. Conventional adhesive hydrogels fail to mitigate mechanical stress owing to their drastically reduced modulus after swelling. This study proposes a novel tension-reducing self-shrinking tough hydrogel patch designed to enhance post-swelling modulus and bioisotropic mechanical reinforcement for anastomotic repair, addressing the limitations of existing materials.
Study design, materials and methods
A dual-network hydrogel system composed of poly(vinyl alcohol) (PVA) and poly(acrylic acid) (PAA) was developed. Directional annealing was applied to optimize crosslinking density and polymer chain alignment in the dry state, enabling modulus retention post-swelling. The hydrogel’s adhesive properties were tailored via physical entanglement. Mechanical performance was evaluated through cyclic tensile testing and swelling assays in simulated bladder conditions (37°C, pH 6.8). A rat bladder enlargement model was established to assess in vivo efficacy, with histological (H&E, trichrome) and immunohistochemical (collagen I/III, α-SMA) analyses quantifying tissue integration, inflammation, and biomechanical reinforcement.
Interpretation of results
This work overcomes the inherent trade-off between hydrogel swelling and modulus degradation by leveraging directional annealing to pre-organize the dual-network structure. Unlike isotropic hydrogels, the bioisotropic design mimics native bladder mechanics, preventing stress concentration at the anastomosis. The self-shrinking behavior dynamically accommodates bladder expansion, while covalent-physical hybrid crosslinking ensures durability under cyclic loading. However, long-term biocompatibility and degradation kinetics require further optimization for clinical translation.