Multifunctional Hyaluronic Acid Microneedle Patch Embedded by Cerium/Zinc-Based Composites for Accelerating Diabetes Wound Healing.
Juan YangZhaoyou ChuYechun JiangWang ZhengJiangwei SunLingling XuYan MaWanni WangMin ShaoHai-Sheng QianPublished in: Advanced healthcare materials (2023)
Chronic 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 Zn 2+ and Ce 3+ / 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.
Keyphrases
- wound healing
- diabetic rats
- oxidative stress
- hyaluronic acid
- nuclear factor
- oxide nanoparticles
- reactive oxygen species
- dna damage
- type diabetes
- cell migration
- signaling pathway
- toll like receptor
- induced apoptosis
- cardiovascular disease
- single cell
- cell proliferation
- ischemia reperfusion injury
- glycemic control
- endothelial cells
- pi k akt
- high fat diet induced
- multiple sclerosis
- genome wide
- cancer therapy
- gene expression
- rna seq
- drug induced
- staphylococcus aureus
- pseudomonas aeruginosa
- drug delivery
- dna methylation
- early onset
- insulin resistance
- epithelial mesenchymal transition
- high glucose
- cardiovascular events
- risk factors
- weight gain
- combination therapy
- immune response
- adipose tissue
- body mass index
- endoplasmic reticulum stress
- heavy metals
- vascular endothelial growth factor
- gold nanoparticles