Glucopeptide Superstructure Hydrogel Promotes Surgical Wound Healing Following Neoadjuvant Radiotherapy by Producing NO and Anticellular Senescence.
Hang WangGanen MuXiaoyao CaiXiaoguang ZhangRuiqi MaoHaixue JiaHongjing LuoJianfeng LiuCuicui ZhaoZhongyan WangCuihong YangPublished in: Advanced healthcare materials (2024)
Neoadjuvant radiotherapy, a preoperative intervention regimen for reducing the stage of primary tumors and surgical margins, has gained increasing attention in the past decade. However, radiation-induced skin damage during neoadjuvant radiotherapy exacerbates surgical injury, remarkably increasing the risk of refractory wounds and compromising the therapeutic effects. Radiation impedes wound healing by increasing the production of reactive oxygen species and inducing cell apoptosis and senescence. Here, a self-assembling peptide (R-peptide) and hyaluronic-acid (HA)-based and cordycepin-loaded superstructure hydrogel is prepared for surgical incision healing after neoadjuvant radiotherapy. Results show that i) R-peptide coassembles with HA to form biomimetic fiber bundle microstructure, in which R-peptide drives the assembly of single fiber through π-π stacking and other forces and HA, as a single fiber adhesive, facilitates bunching through electrostatic interactions. ii) The biomimetic superstructure contributes to the adhesion and proliferation of cells in the surgical wound. iii) Aldehyde-modified HA provides dynamic covalent binding sites for cordycepin to achieve responsive release, inhibiting radiation-induced cellular senescence. iv) Arginine in the peptides provides antioxidant capacity and a substrate for the endogenous production of nitric oxide to promote wound healing and angiogenesis of surgical wounds after neoadjuvant radiotherapy.
Keyphrases
- radiation induced
- wound healing
- locally advanced
- rectal cancer
- radiation therapy
- nitric oxide
- hyaluronic acid
- lymph node
- early stage
- squamous cell carcinoma
- drug delivery
- randomized controlled trial
- endothelial cells
- reactive oxygen species
- dna damage
- patients undergoing
- cell proliferation
- staphylococcus aureus
- oxidative stress
- amino acid
- pseudomonas aeruginosa
- escherichia coli
- white matter
- endoplasmic reticulum stress
- vascular endothelial growth factor
- cell cycle arrest