Carbon Dots’ Potential in Wound Healing: Inducing M2 Macrophage Polarization and Demonstrating Antibacterial Properties for Accelerated Recovery

伤口愈合 炎症 巨噬细胞极化 脂多糖 体内 成纤维细胞 血管生成 巨噬细胞 免疫学 医学 化学 癌症研究 体外 生物 生物化学 生物技术
作者
Rajesh Gujju,Saikat Dewanjee,Kamini Singh,Sai Balaji Andugulapati,Satya Krishna Tirunavalli,Vinod Kumar Jaina,Ramesh Kandimalla,Sunil Misra,Nagaprasad Puvvada
出处
期刊:ACS applied bio materials [American Chemical Society]
卷期号:6 (11): 4814-4827 被引量:13
标识
DOI:10.1021/acsabm.3c00578
摘要

Bacterial infections and persistent inflammation can impede the intrinsic healing process of wounds. To combat this issue, researchers have delved into the potential use of carbon dots (CDs) in the regulation of inflammation and counteract infections. These CDs were synthesized using a microwave-assisted hydrothermal process and have demonstrated outstanding antibacterial and antibiofilm properties against Gram-positive and Gram-negative bacteria. Additionally, CDs displayed biocompatibility at therapeutic concentrations and the ability to specifically target mitochondria. CD treatment effectively nullified lipopolysaccharide-triggered reactive oxygen species production by macrophages, while simultaneously promoting macrophage polarization toward an anti-inflammatory phenotype (M2), leading to a reduction in inflammation and an acceleration in wound healing. In vitro scratch assays also revealed that CDs facilitated the tissue-repairing process by stimulating epithelial cell migration during reepithelialization. In vivo studies using CDs topically applied to lipopolysaccharide (LPS)-stimulated wounds in C57/BL6 mice demonstrated significant improvements in wound healing due to enhanced fibroblast proliferation, angiogenesis, and collagen deposition. Crucially, histological investigations showed no indications of systemic toxicity in vital organs. Collectively, the application of CDs has shown immense potential in speeding up the wound-healing process by regulating inflammation, preventing bacterial infections, and promoting tissue repair. These results suggest that further clinical translation of CDs should be considered.
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