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Updated: Jan 10, 2026

Engineering a Bilayered Hydrogel to Control ASC Differentiation
Published on: May 25, 2012
Oxygenating Nanobubble Hydrogel for Accelerated Surgical Wound Closure and Restoration of Native Skin Architecture
Xiaoxue Han1,2,3,4, Anika Bushra1,2, Wen Ren1,2
1Department of Bioengineering, University of Illinois at Urbana-Champaign, 1102 Everitt Lab, 1406 West Green Street, Urbana, Illinois 61801, United States.
Abstract:
Prolonged hypoxia and inflammation are critical barriers in postsurgical care, often leading to delayed healing and excessive scarring, which are complications that standard passive dressings fail to address. Here, we engineer a translationally focused oxygen-nanobubble-laden hydrogel (ONB-Gel) that actively orchestrates a phase-specific healing cascade. Composed of stable sodium alginate nanobubbles within a Carbopol matrix, the ONB-Gel provides a sustained oxygen source directly to the wound bed. In a clinically relevant rat surgical wound model, the application of ONB-Gel markedly outperformed the standard-of-care dressing (Adaptic), accelerating complete wound closure by over 25% and reducing the final scar width by more than 50%. Mechanistically, the ONB-Gel resolves tissue hypoxia, significantly downregulating inflammatory cytokines (IL-6, TNF-α), oxidative stress, and the chronic hypoxia marker. Critically, beyond accelerating closure, ONB-Gel promotes tissue regeneration, evidenced by dense, functionally aligned collagen deposition and the restoration of a near-normal epidermal architecture, unattainable with conventional dressings. Overall, ONB-Gel represents a promising platform for enhancing both the rate and the quality of postsurgical wound repair.
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