School of Pharmacy, Yantai University, 30# Qingquan Road, Yantai 264005, PR China.
College of Marine Life Science, Ocean University of China, 5# Yushan 10 Road, Qingdao 266003, PR China.
Colloids Surf B Biointerfaces. 2024 Sep;241:114049. doi: 10.1016/j.colsurfb.2024.114049. Epub 2024 Jun 19.
The colonisation of microorganisms such as bacteria forms a biofilm barrier on the wound's surface, preventing or delaying the penetration of antibacterial drugs. At the same time, continuous bacterial infection can cause oxidative stress and an inflammatory response and hinder angiogenesis, resulting in difficult wound healing. Based on the "one stone, three birds" strategy, a multi-functional nanoparticle composite soluble microneedle was designed and developed to solve this dilemma better. Ginsenoside-liposomes(R-Lipo) were prepared by ginsenoside Rg3, which had the effect of promoting repair, instead of cholesterol, and loaded with berberine (Ber), the antibacterial component of Coptis, together with polydopamine (PDA), which had anti-inflammatory and antioxidant properties, into microneedles based on hyaluronic acid (PDA/R-Lipo@BerMN). PDA/R-Lipo@BerMN tip can penetrate and destroy the integrity of the biofilm, dissolve under the action of hyaluronidase in the skin, and gradually release the drug to achieve rapid antibacterial, anti-inflammatory, antioxidant, and proliferation. As expected, the PDA/R-Lipo@BerMN patch effectively cleared ROS during wound closure, further promoted M2 macrophage polarisation, eradicated bacterial infection, and regulated the immune microenvironment, promoting inflammation suppression, collagen deposition, angiogenesis, and tissue regeneration.
微生物(如细菌)的定植在创面表面形成生物膜屏障,防止或延迟抗菌药物的渗透。同时,持续的细菌感染会引起氧化应激和炎症反应,并阻碍血管生成,导致伤口愈合困难。基于“一石三鸟”的策略,设计并开发了一种多功能纳米颗粒复合可溶性微针,以更好地解决这一困境。人参皂苷 Rg3 代替胆固醇制备了人参皂苷脂质体(R-Lipo),并负载了黄连中的抗菌成分小檗碱(Ber),以及具有抗炎和抗氧化特性的聚多巴胺(PDA),制成了基于透明质酸的微针(PDA/R-Lipo@BerMN)。PDA/R-Lipo@BerMN 针尖可以穿透并破坏生物膜的完整性,在皮肤中的透明质酸酶作用下溶解,并逐渐释放药物,从而实现快速的抗菌、抗炎、抗氧化和增殖作用。正如预期的那样,PDA/R-Lipo@BerMN 贴片在伤口闭合过程中有效清除了 ROS,进一步促进了 M2 巨噬细胞的极化,根除了细菌感染,并调节了免疫微环境,促进了炎症抑制、胶原沉积、血管生成和组织再生。