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Preparation of Multifunctional Hydrogels with In Situ Dual Network Structure and Promotion of Wound Healing.

Authors :
Lu Y
Hu M
Huang Y
Liao J
Zhao M
Zhou Y
Xia G
Zhan Q
Source :
Biomacromolecules [Biomacromolecules] 2024 Aug 12; Vol. 25 (8), pp. 4965-4976. Date of Electronic Publication: 2024 Jul 15.
Publication Year :
2024

Abstract

As an emerging biomedical material, wound dressings play an important therapeutic function in the process of wound healing. It can provide an ideal healing environment while protecting the wound from a complex external environment. A hydrogel wound dressing composed of tilapia skin gelatin (Tsg) and fucoidan (Fuc) was designed in this article to enhance the microenvironment of wound treatment and stimulate wound healing. By mixing horseradish peroxidase (HRP), hydrogen peroxide (H <subscript>2</subscript> O <subscript>2</subscript> ), tilapia skin gelatin-tyramine (Tsg-Tyr), and carboxylated fucoidan-tyramine in agarose (Aga), using the catalytic cross-linking of HRP/H <subscript>2</subscript> O <subscript>2</subscript> and the sol-gel transformation of Aga, a novel gelatin-fucoidan (TF) double network hydrogel wound dressing was constructed. The TF hydrogels have a fast and adjustable gelation time, and the addition of Aga further enhances the stability of the hydrogels. Moreover, Tsg and Fuc are coordinated with each other in terms of biological efficacy, and the TF hydrogel demonstrated excellent antioxidant properties and biocompatibility in vitro . Also, in vivo wound healing experiments showed that the TF hydrogel could effectively accelerate wound healing, reduce wound microbial colonization, alleviate inflammation, and promote collagen deposition and angiogenesis. In conclusion, TF hydrogel wound dressings have the potential to replace traditional dressings in wound healing.

Details

Language :
English
ISSN :
1526-4602
Volume :
25
Issue :
8
Database :
MEDLINE
Journal :
Biomacromolecules
Publication Type :
Academic Journal
Accession number :
39007721
Full Text :
https://doi.org/10.1021/acs.biomac.4c00403