Multipronged Micelles-Hydrogel for Targeted and Prolonged Drug Delivery in Chronic Wound Infections.
Qian ZhaoJuan LiuSuhan LiuJunhua HanYingxian ChenJianzhong ShenKui ZhuXiaowei MaPublished in: ACS applied materials & interfaces (2022)
Chronic diabetic wounds are a growing threat globally. Many aspects contribute to its deterioration, including bacterial infection, unbalanced microenvironment, dysfunction of cell repair, etc. In this work, we designed a multipronged micelles-hydrogel platform loaded with curcumin and rifampicin (CRMs-hydrogel) for bacteria-infected chronic wound treatment. The curcumin- and rifampicin-loaded micelles (CRMs) exhibited both MMP9-responsive and epidermal growth factor receptor (EGFR)-targeting abilities. On the one hand, drugs could be released from micelles due to responsive disassembly by MMP9, a matrix metalloproteinase overexpressed in a chronic wound environment; on the other hand, CRMs showed specific targeting to EGFR on epithelial cells and fibroblasts and therefore increased intracellular drug delivery. The thermosensitive CRMs-hydrogel could form strong adhesion with the wound area and served as a suitable matrix for sustained release of CRMs directly at the wound bed, with excellent intracellular and extracellular bacterial elimination efficiency and wound healing promotion capability. We found that a single dose of CRMs-hydrogel achieved 99% antibacterial rate at the MRSA-infected diabetic wound, which effectively reduced inflammatory response and promoted the neovascularization and re-epithelialization process, with nearly half reduction of the skin barrier regeneration period. Collectively, our thermosensitive, MMP9-responsive, and targeted micelles-hydrogel nanoplatform is promising for chronic wound treatment.
Keyphrases
- wound healing
- cancer therapy
- drug delivery
- epidermal growth factor receptor
- drug release
- inflammatory response
- small cell lung cancer
- tyrosine kinase
- stem cells
- staphylococcus aureus
- type diabetes
- advanced non small cell lung cancer
- pseudomonas aeruginosa
- mesenchymal stem cells
- hyaluronic acid
- escherichia coli
- oxidative stress
- surgical site infection
- cell migration
- extracellular matrix
- cell therapy
- toll like receptor
- biofilm formation