伤口愈合
脂质体
材料科学
生物医学工程
巨噬细胞极化
炎症
微流控
巨噬细胞
纳米技术
医学
化学
免疫学
生物化学
体外
作者
Yue Zhi,Junyi Che,Haofang Zhu,Rui Liu,Yuanjin Zhao
标识
DOI:10.1002/adfm.202304353
摘要
Abstract In diabetic wound healing, M1 macrophage accumulation and elevated inflammation are prevalent issues. Intelligent delivery systems that can sustainably release antioxidizing and anti‐inflammatory ingredients are expected for effective wound healing. Herein, a novel glycyrrhetinic acid (GA) liposomes encapsulated microcapsules delivery system that has desired features for inflammatory wound repair is presented. As the bacteria could break down the alginate shells, the GA liposomes could be controllably released from the microcapsules, which promotes M2 macrophage polarization and regulate their responses in the inflammatory wound microenvironment. Based on these, it is demonstrated that the GA liposomes encapsulated microcapsules delivery system exhibits an anti‐inflammatory and immunomodulatory effect for diabetic wound healing in a full‐thickness defect model in diabetic rats. These results indicate that the immunomodulatory capabilities of the microcapsules can be unitized for efficient wound repair, and such a delivery system is valuable for clinical wound healing applications.
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