Multifunctional Hyaluronic Acid Microneedle Patch Embedded by Cerium/Zinc‐Based Composites for Accelerating Diabetes Wound Healing

Author:

Yang Juan1,Chu Zhaoyou1,Jiang Yechun2,Zheng Wang2,Sun Jiangwei2,Xu Lingling2,Ma Yan2,Wang Wanni2,Shao Min3,Qian Haisheng24ORCID

Affiliation:

1. Department of Pharmacology School of Basic Medical Sciences Anhui Medical University Hefei 230032 P. R. China

2. School of Biomedical Engineering Anhui Provincial Institute of Translational Medicine Anhui Medical University Hefei 230032 P. R. China

3. Department of Critical Care Medicine The First Affiliated Hospital of Anhui Medical University Hefei 230032 P. R. China

4. Institute of Health and Medicine Hefei Comprehensive National Science Center Hefei 230601 P. R. China

Abstract

AbstractChronic nonhealing diabetic wounds are becoming increasingly severe, with high rates of mortality and disability, owing to the difficulty in wound healing caused by hyperglycemia, blocked angiogenesis, biofilm infection, and excessive oxidative stress. A multicomponent enzyme‐responsive natural polymer, a hyaluronic acid (HA) microneedle, embedded in a cerium/zinc‐based nanomaterial (ZCO) for the treatment of diabetic wounds is reported. ZCO‐HA can destroy the oxidation balance of bacteria, kill bacteria, and scavenge reactive oxygen species (ROS) to alleviate oxidative stress via the adjustable release of Zn2+ and Ce3+/4+. Additionally, ZCO‐HA exhibits good anti‐inflammatory activity through the nuclear factor kappa‐B (NF‐κB) pathway, which reduces the inflammatory state of macrophages and promotes cell proliferation, migration, and angiogenesis. In vitro experiments shows that ZCO‐HA accompanies mouse fibroblast migration, promoting human umbilical vein endothelial cell tube formation. In vivo studies in mice with streptozotocin‐induced (STZ)‐induced diabetes reveal that this microneedle accelerates wound healing without systemic toxicity. RNA transcriptome sequencing illustrates that the multicomponent HA microneedle accelerates wound healing in diabetes through cell migration and inhibits inflammatory reactions and oxidative damage in mice via the NF‐κB signaling pathway.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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