Xiong Shiyu, Ding Xingwei, Zhou Ling, Liu Ziqian, Jiang Wenyan, Ai Fanrong, Cai Kaiyong
The National Engineering Research Center for Bioengineering Drugs and the Technologies, Jiangxi Provincial Key Laboratory of Bioengineering Drugs, Institute of Translational Medicine, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi 330038, PR China.
The National Engineering Research Center for Bioengineering Drugs and the Technologies, Jiangxi Provincial Key Laboratory of Bioengineering Drugs, Institute of Translational Medicine, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi 330038, PR China.
J Colloid Interface Sci. 2025 Apr;683(Pt 2):357-371. doi: 10.1016/j.jcis.2024.12.138. Epub 2024 Dec 25.
The management of diabetic wounds (DW) is a significant challenge within the medical field. Effectively regulating the levels of reactive oxygen species (ROS) at the wound site and orchestrating the inflammatory response are effective strategies for DW treatment. In this study, a novel hydrogel was developed by cross-linking polyboronic acid-modified carboxymethyl chitosan with herbal active ingredient rosmarinic acid (RA), an active herbal ingredient, through dynamic boronic esters formation. In this RA hydrogel (RAgel), RA serves both as an active pharmaceutical ingredient and as a linker for the creation of a dynamic covalent hydrogel, which can decrease the potential toxicity of chemical crosslinking agents and improve the utilization of RA. RAgel demonstrated potential for controlling RA loading and responsiveness to ROS and glucose levels in a diabetic wound environment. Additionally, the intrinsic antioxidant and antibacterial properties of RA were effectively preserved and enhanced upon integration into RAgel. Furthermore, RAgel not only promoted the migration of L929 cells, a key aspect of tissue repair, but also induced M2 polarization in macrophages,while inhibiting the secretion of pro-inflammatory cytokines. In a murine model of diabetic wound healing, RAgel significantly enhanced the proliferation of both the epidermal and granulation tissues. It also exerts a marked anti-inflammatory effect and promotes collagen deposition, thereby expediting the overall wound healing process. The reported RAgel formulation has potential to address the complex challenges associated with diabetic wound management.
糖尿病伤口(DW)的管理是医学领域一项重大挑战。有效调节伤口部位活性氧(ROS)水平并协调炎症反应是治疗糖尿病伤口的有效策略。在本研究中,通过动态硼酸酯形成反应,将聚硼酸修饰的羧甲基壳聚糖与草药活性成分迷迭香酸(RA)交联,开发出一种新型水凝胶。在这种RA水凝胶(RAgel)中,RA既作为活性药物成分,又作为形成动态共价水凝胶的连接剂,这可以降低化学交联剂的潜在毒性,并提高RA的利用率。RAgel在糖尿病伤口环境中显示出控制RA负载以及对ROS和葡萄糖水平作出响应的潜力。此外,RA的固有抗氧化和抗菌特性在整合到RAgel中后得到有效保留和增强。此外,RAgel不仅促进了组织修复关键方面的L929细胞迁移,还诱导巨噬细胞向M2极化,同时抑制促炎细胞因子的分泌。在糖尿病伤口愈合的小鼠模型中,RAgel显著增强了表皮组织和肉芽组织的增殖。它还发挥显著的抗炎作用并促进胶原蛋白沉积,从而加速整体伤口愈合过程。所报道的RAgel制剂有潜力应对与糖尿病伤口管理相关的复杂挑战。