Jia Mengjie, Miao Wenjun, Li Yiliang, Guo Yajie, Zeng Jieying, Gao Yan, Li Xinting, Wang Yufan, Zhao Zhenghuan, Xu Zichen, Wang Nancy, Yang Fang, Zhao Jing, Wang Yi, Wang Guixue
School of Basic Medical Sciences, Chongqing Medical University, Chongqing 400016, China.
The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, China.
Innovation (Camb). 2024 Dec 27;6(4):100761. doi: 10.1016/j.xinn.2024.100761. eCollection 2025 Apr 7.
This study leverages the unique advantages of polyprodrug systems and biomimetic technology to develop a novel biomimetic nanoformulation, in which neutrophil extracellular vesicles (NEVs) are coated onto reactive oxygen species (ROS)-sensitive probucol-based polyprodrug nanoparticles (NPPBNPs). This NEV-camouflaged biomimetic nanoformulation holds significant potential for the effective treatment of cerebral ischemia-reperfusion injury (CIRI), offering multifaceted therapeutic effects, such as ROS elimination, inhibition of oxidative stress-induced neuronal apoptosis, attenuation of glial hyperactivation, and suppression of pro-inflammatory mediator secretion. In a murine CIRI model, NPPBNPs markedly enhanced neuronal viability, ameliorated the ischemic penumbra, restored behavioral functions, and exhibited an acceptable safety profile. The therapeutic mechanism of NPPBNPs involves NEV-mediated camouflage, which enables selective targeting of the pathological endothelium, thereby reducing peripheral neutrophil recruitment and facilitating blood-brain barrier (BBB) transport. Upon internalization by neurons, astrocytes, and microglia within ischemic regions, NPPBNPs respond to elevated intracellular ROS levels by releasing probucol in a controlled manner, which synergistically mitigates oxidative stress and inflammatory responses in CIRI-affected areas. Collectively, this multifunctional biomimetic nanoformulation represents a promising and practical strategy for the safe and effective treatment of CIRI.
本研究利用多聚前药系统和仿生技术的独特优势,开发了一种新型仿生纳米制剂,其中中性粒细胞胞外囊泡(NEVs)被包覆在基于普罗布考的活性氧(ROS)敏感型多聚前药纳米颗粒(NPPBNPs)上。这种NEV伪装的仿生纳米制剂在有效治疗脑缺血再灌注损伤(CIRI)方面具有巨大潜力,具有多方面的治疗效果,如消除ROS、抑制氧化应激诱导的神经元凋亡、减轻胶质细胞过度活化以及抑制促炎介质分泌。在小鼠CIRI模型中,NPPBNPs显著提高了神经元活力,改善了缺血半暗带,恢复了行为功能,并表现出可接受的安全性。NPPBNPs的治疗机制涉及NEV介导的伪装,这使得能够选择性靶向病理性内皮,从而减少外周中性粒细胞募集并促进血脑屏障(BBB)转运。在缺血区域的神经元、星形胶质细胞和小胶质细胞内化后,NPPBNPs通过以可控方式释放普罗布考来响应细胞内ROS水平的升高,这协同减轻了CIRI影响区域的氧化应激和炎症反应。总的来说,这种多功能仿生纳米制剂代表了一种安全有效治疗CIRI的有前景且实用的策略。