Copper doped carbon dots modified bacterial cellulose with enhanced antibacterial and immune regulatory functions for accelerating wound healing.
Yingyu LiuYifan ZhaoSusu GuoDanlei QinJingyu YanHuaiyi ChengJian ZhouJianing RenLingxiang SunHongyi PengXiuping WuBing LiPublished in: Carbohydrate polymers (2024)
The microenvironment of wound healing is susceptible to bacterial infection, chronic inflammation, oxidative stress, and inadequate angiogenesis, requiring the development of innovative wound dressings with antibacterial, anti-inflammatory, antioxidant, and angiogenic capabilities. This research crafted a new multifunctional bacterial cellulose composite membrane infused with copper-doped carbon dots (BC/Cu(II)-RCDs). Findings validated the successful loading of copper-doped carbon dots onto the BC membrane via hydrogen bonding interactions. Compared to the pure BC membrane, the BC/Cu(II)-RCDs composite membrane exhibited significantly enhanced hydrophilicity, tensile properties, and thermal stability. Diverse in vitro assays demonstrated excellent biocompatibility and antibacterial activity of BC/Cu(II)-RCDs composite membranes, alongside their ability to expedite the inflammatory phase and stimulate angiogenesis. In vivo trials corroborated the membrane's ability to foster epithelial regeneration, collagen deposition, and tissue regrowth in full-thickness skin wounds in rats while also curbing inflammation in infected full-thickness skin wounds. More importantly, the treatment of the BC/Cu(II)-RCDs composite membrane may result in the activation of VEGF and MAPK signaling proteins, which are key players in cell migration, angiogenesis, and skin tissue development. In essence, the developed BC/Cu(II)-RCDs composite membrane shows promise for treating infected wounds and serves as a viable alternative material for medicinal bandages.
Keyphrases
- wound healing
- oxidative stress
- metal organic framework
- quantum dots
- vascular endothelial growth factor
- anti inflammatory
- stem cells
- endothelial cells
- cell migration
- dna damage
- ionic liquid
- machine learning
- drug delivery
- silver nanoparticles
- signaling pathway
- transcription factor
- cancer therapy
- induced apoptosis
- ischemia reperfusion injury
- drug induced
- optical coherence tomography
- highly efficient
- tissue engineering
- pi k akt