纳米凝胶
脊髓损伤
神经保护
化学
布洛芬
可重用性
控制释放
脊髓
药物输送
纳米纤维
自愈水凝胶
小胶质细胞
罗亚
阻塞(统计)
材料科学
纳米技术
纳米颗粒
神经系统
块(置换群论)
作者
Zhijian Wei,Susu Huang,Wencan Zhang,Jiayao Wen,Xiaolong Zhou,Wei He,Xiaoye Yang,Haifeng Wang,Guangxi Zhai,Bin Shi,Lin Jin,DACHUAN WANG,Shiqing Feng,Lei Ye
标识
DOI:10.1002/advs.202510976
摘要
Abstract Spinal cord injury (SCI), a highly disabling injury to the central nervous system, has a complex and sequential pathogenesis. Traditional multiple‐delivery systems rely on a physical mix of nanoparticles or drugs in hydrogels, which lacks the controllability of the drug. To solve these problems, an integrative hydrogel system cross‐linked with a Per‐g‐PSB nanogel is designed. Dendritic macromolecular nanogels (Per‐g‐PSB) could not only act as cross‐linkers to adjust the hydrogel mechanical properties but also form a dynamic network (Dex/Per‐g‐PSB hydrogel). Most importantly, a large amount of charge could lead to a significant sustained release via electrostatic interactions. The hydrogel platform (Mel/Ibu@D/P‐g‐PSB) realizes the sequential release of melatonin and ibuprofen by different mechanisms. Melatonin is first released by diffusion and exhibits significant neuroprotective effects during the acute phase by downregulating the expression of inflammatory cytokines. Ibuprofen is released in the second stage due to strong electrostatic interactions, and it reduces RhoA signaling activation by blocking the ROCK pathway in the subacute phase, which reduces the deleterious cascade reaction after spinal cord injury. These results show that the ion‐sensitive hydrogel platform with sequentially releasing drug effects, combining anti‐inflammatory effects and blocking the ROCK pathway, shows excellent repair of SCI.
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