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用于缺血性中风协同治疗的模块化组装仿生纳米气泡:级联调节血栓炎症网络

Modular assembled biomimetic nanobubbles for synergistic therapy of ischemic stroke cascade modulation thrombo-inflammatory network.

作者信息

Li Mingxi, Xu Xuan, Tang Guoyan, Wu Huan, Wang Yakun, Cheng Chen, Liu Hongde, Yang Fang

机构信息

Department of Cardiology, Zhongda Hospital Affiliated to Southeast University, 87 Dingjiaqiao, Nanjing, 210009, PR China.

State Key Laboratory of Digital Medical Engineering, School of Biological Sciences and Medical Engineering, Southeast University, Nanjing, 210096, PR China.

出版信息

Bioact Mater. 2025 Jul 1;52:753-772. doi: 10.1016/j.bioactmat.2025.06.054. eCollection 2025 Oct.

Abstract

Dynamic pathology-adaptive nanodelivery systems represent a promising frontier in acute ischemic stroke (AIS) therapy. Here, we report a thrombo-inflammatory cascade-targeted biomimetic nanobubble engineered through gas-liquid interfacial modular assembly of platelet membranes and immunomodulator fingolimod (FTY720). Molecular dynamics simulations uncovered a gas-liquid interfacial self-organization mechanism driving the ordered spatial distribution of platelet membrane lipid rafts and amphiphilic FTY720 to fabricate platelet membrane coated FTY720 nanobubble (PFNB). Such modular assembled PFNBs can promote the effective presentation of targeted proteins and drug molecular functions on the biointerface, enabling precise sequential lesion targeting, enhanced blood-brain barrier penetration and inflammatory microglial uptake, significantly improving drug delivery efficiency. Therapeutic efficacy analysis whole-genome RNA sequencing demonstrated a virtuous cycle between anti-inflammatory regulation and vascular protection, ultimately mitigating the brain tissue damage. Therefore, PFNBs provide a paradigm for the modular construction and biointerface efficacy regulation of multifunctional integrated biomimetic nano-delivery systems, offering promising strategies for multi-target synergistic treatment of AIS.

摘要

动态病理学适应性纳米递送系统是急性缺血性中风(AIS)治疗中一个很有前景的前沿领域。在此,我们报告了一种通过血小板膜与免疫调节剂芬戈莫德(FTY720)的气液界面模块化组装而设计的血栓炎症级联靶向仿生纳米气泡。分子动力学模拟揭示了一种气液界面自组织机制,该机制驱动血小板膜脂筏和两亲性FTY720的有序空间分布,从而制造出血小板膜包被的FTY720纳米气泡(PFNB)。这种模块化组装的PFNB可以促进靶向蛋白和药物分子功能在生物界面上的有效呈现,实现精确的顺序性病灶靶向、增强血脑屏障穿透和炎症性小胶质细胞摄取,显著提高药物递送效率。治疗效果分析和全基因组RNA测序表明,抗炎调节和血管保护之间存在良性循环,最终减轻脑组织损伤。因此,PFNB为多功能集成仿生纳米递送系统的模块化构建和生物界面功效调节提供了一个范例,为AIS的多靶点协同治疗提供了有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fe2/12271911/d9bc69a66e77/ga1.jpg

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