Spider Silk‐Inspired Hyaluronic Acid‐Based Hydrogels with Superior Self‐Healing Capability and Enhanced Strength

Author:

Yang Kaidan1,Zhou Ding2,Wang Yachao1,Chen Ruina1,Dong Qi1,Xiao Pu3,Zhou Yingshan1,Zhang Jing45ORCID

Affiliation:

1. State Key Laboratory of New Textile Materials and Advanced Processing Technologies Wuhan Textile University Wuhan 430073 P. R. China

2. Department of Biomedical Engineering TaiKang Medical School (School of Basic Medical Sciences) Wuhan University Wuhan 430071 P. R. China

3. State Key Laboratory of High Performance Ceramics and Superfine Microstructure Shanghai Institute of Ceramics Chinese Academy of Sciences Shanghai 200050 P. R. China

4. Future Industries Institute University of South Australia Mawson Lakes, SA 5095 Australia

5. Department of Chemical and Biological Engineering Monash University Clayton, VIC 3800 Australia

Abstract

AbstractHyaluronic acid hydrogels are promising materials for diverse applications, yet their potential is hampered by limitations such as low self‐healing efficiency and insufficient mechanical strength. Inspired by the heterogeneous structures of spider silk, we introduce a novel dual dynamically crosslinked network hydrogel. This hydrogel comprises an acylhydrazone‐crosslinked network, utilizing aldehyde hyaluronic acid (AHA) and 3,3′‐dithiobis (propionohydrazide) (DTP) as a first network, and a secondary network formed by hydrogen bonds‐crosslinked network between tannic acid (TA) and silk fibroin (SF) with β‐sheet formation. The hydrogel exhibits exceptional self‐healing ability due to the dynamic and reversible nature of Schiff base bonds, disulfide bonds, and hydrogen bonds, achieving complete healing within 5 minutes. Additionally, the spider silk‐inspired heterogeneous structures enhance mechanical properties. Furthermore, the incorporation of TA provides enhances adhesion, as well as remarkable antibacterial and antioxidant properties. This innovative hyaluronic acid‐based hydrogel, inspired by spider silk, offers a promising avenue to fortify both the mechanical strength and self‐healing capabilities of hydrogels, thus expanding opportunities for applications in tissue engineering and biomedicine.

Publisher

Wiley

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