A Bilayer Polyurethane Patch with Sustained Growth Factor Release and Antibacteria for Re-epithelization of Large-Scale Oral Mucosal Defects.
Qiao ZhangJinlin ChenTianyu ZhangDan LiuXirui LongJiehua LiLu JiangYanchao WangHong TanPublished in: ACS applied materials & interfaces (2024)
In the field of oral and maxillofacial surgery, extensive oral soft-tissue injuries occur repeatedly in clinical practice; however, effective restorative materials are lacking. In this study, a biodegradable waterborne polyurethane patch featuring a mucosa bionic bilayer structure is presented. This patch consists of a porous scaffold layer that faces the lesion, incorporating a polydopamine coating to achieve sustained release of epidermal growth factors (EGFs) for mucosal defect reconstruction. Additionally, there is a dense barrier layer toward the oral cavity loaded with silver nanoparticles, which prevents bacteria from entering the wound and simultaneously acts as a physical barrier. This patch can sustainably release EGF in vitro for 2 weeks, thereby facilitating the proliferation and migration of HaCaT and L929 cells, while effectively killing common oral cavity bacteria. In a rabbit buccal mucosal full-thickness defect model, the patch demonstrates better efficacy than the clinical benchmark, decellularized extracellular matrix (dECM). It effectively reduces wound inflammation and significantly upregulates gene expression associated with epithelialization by activating the EGF/epidermal growth factor receptor (EGFR) pathway. These mechanisms promote the proliferation, differentiation, and migration of epithelial/keratinocyte cells, ultimately expediting mucosal defect healing and wound closure.
Keyphrases
- growth factor
- epidermal growth factor receptor
- extracellular matrix
- induced apoptosis
- gene expression
- silver nanoparticles
- tyrosine kinase
- ulcerative colitis
- tissue engineering
- signaling pathway
- cell cycle arrest
- surgical site infection
- wound healing
- clinical practice
- drug delivery
- soft tissue
- advanced non small cell lung cancer
- oxidative stress
- small cell lung cancer
- dna methylation
- minimally invasive
- endoplasmic reticulum stress
- physical activity
- cell death
- coronary artery bypass
- cancer therapy
- pi k akt
- coronary artery disease
- percutaneous coronary intervention
- metal organic framework