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一种具有精确靶向-渗透和高效协同治疗缺血性中风功能的仿生多功能纳米平台。

A Biomimetic Multifunctional Nanoplatform with Precise Targeting-Penetration and Efficient Synergistic Therapy for Ischemic Stroke.

作者信息

Li Xi-Sheng, Li Hui-Yin, Peng Dan, Liu Hong-Rui, Wu Lin, Wang Kai-Jia, Han Yu, Tang Ting-Ting, Hu Zhong-Yang, Peng Jun, Wang Xiaoying, Luo Xiu-Ju

机构信息

Department of Laboratory Medicine, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P. R. China.

Department of Neurology, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2025 Jul 16;17(28):39925-39954. doi: 10.1021/acsami.5c01878. Epub 2025 Jul 4.

Abstract

Ischemic stroke poses a significant threat to public health, and its therapeutic efficacy is limited by blood-brain barrier permeability and multifactorial pathophysiology (such as oxidative stress and inflammation). In this study, a self-assembled metal-organic framework (Zn-DB) was decorated with CeO nanoparticles to construct the CZB nanocomposite with antioxidative and antiapoptotic properties. The CZB-D-A multifunctional nanocomposite was developed by co-loading deferoxamine and an anti-C5a aptamer, and CZB-D-A was camouflaged with neutrophil-like membranes modified with RVG to synthesize a biomimetic nanoplatform (RH@CZB-D-A) for precise targeting and penetration of the blood-brain barrier as well as immune evasion. Consequently, this nanoplatform precisely delivered therapeutic agents and released them better in the acidic lesion owing to its pH-acid response. It was designed to depolarize microglia from the destructive M1 phenotype to the protective M2 phenotype and alleviate ischemia-reperfusion injury by suppressing neuroinflammation, scavenging reactive oxygen species, and mitigating oxidative stress. Meanwhile, it synergistically promoted neuroprotection by multiple mechanisms of antioxidation, antiapoptosis, antiferroptosis, and anti-inflammation, both in vitro and in vivo. Additionally, administration of RH@CZB-D-A to MCAO mice not only enhanced neuronal regeneration but also improved neurological deficits and promoted spatial memory and learning ability. Therefore, this study could bring an alternative approach for developing promising therapeutic strategies against ischemic stroke for clinical applications.

摘要

缺血性中风对公众健康构成重大威胁,其治疗效果受到血脑屏障通透性和多因素病理生理学(如氧化应激和炎症)的限制。在本研究中,一种自组装金属有机框架(Zn-DB)用CeO纳米颗粒进行修饰,以构建具有抗氧化和抗凋亡特性的CZB纳米复合材料。通过共负载去铁胺和抗C5a适配体开发了CZB-D-A多功能纳米复合材料,并用RVG修饰的中性粒细胞样膜对CZB-D-A进行伪装,以合成一种仿生纳米平台(RH@CZB-D-A),用于精确靶向和穿透血脑屏障以及免疫逃逸。因此,由于其pH酸响应,该纳米平台能够精确递送治疗剂并在酸性病变中更好地释放它们。它旨在使小胶质细胞从具有破坏性的M1表型转变为具有保护性的M2表型,并通过抑制神经炎症、清除活性氧和减轻氧化应激来减轻缺血再灌注损伤。同时,它在体外和体内通过抗氧化、抗凋亡、抗铁死亡和抗炎等多种机制协同促进神经保护。此外,对大脑中动脉闭塞(MCAO)小鼠施用RH@CZB-D-A不仅增强了神经元再生,还改善了神经功能缺损,并促进了空间记忆和学习能力。因此,本研究可为开发有前景的缺血性中风治疗策略以供临床应用带来一种替代方法。

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