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Ultrasound‐Responsive HBD Peptide Hydrogel with Antibiofilm Capability for Fast Diabetic Wound Healing.

Authors :
Zong, Lanlan
Teng, Runxin
Zhang, Huiqi
Liu, Wenshang
Feng, Yu
Lu, Zhengmao
Zhou, Yuxiao
Fan, Zhen
Li, Meng
Pu, Xiaohui
Source :
Advanced Science. 11/13/2024, Vol. 11 Issue 42, p1-18. 18p.
Publication Year :
2024

Abstract

Despite advancements in therapeutic agents for diabetic chronic wounds, challenges such as suboptimal bioavailability, intricate disease milieus, and inadequate delivery efficacy have impeded treatment outcomes. Here, ultrasound‐responsive hydrogel incorporated with heparin‐binding domain (HBD) peptide nanoparticles is developed to promote diabetic wound healing. HBD peptide, derived from von Willebrand Factor with angiogenic activity, are first engineered to self‐assemble into nanoparticles with enhanced biostability and bioavailability. Ultrasound responsive cargo release and hydrogel collapses are first verified through breakage of crosslinking. In addition, desired antioxidant and antibacterial activity of such hydrogel is observed. Moreover, the degradation of hydrogel under ultrasound stimulation into smaller fragments facilitated the deeper wound penetration of ≈400 µm depth. Complete wound closure is observed from diabetic mice with chronic wounds after being treated with the proposed hydrogel. In detail, in vivo studies revealed that hydrogels loaded with HBD peptide nanoparticles increased the levels of angiogenesis‐related growth factors (VEGF‐A, CD31, and α‐SMA) to effectively accelerate wound repair. Overall, this study demonstrates that ultrasound‐responsive HBD peptide hydrogel provides a synergistic therapeutic strategy for external biofilm elimination and internal effective delivery for diabetic wounds with biofilm infection. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
21983844
Volume :
11
Issue :
42
Database :
Academic Search Index
Journal :
Advanced Science
Publication Type :
Academic Journal
Accession number :
180851699
Full Text :
https://doi.org/10.1002/advs.202406022