Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin, 130022, P. R. China.
School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei, Anhui, 230029, P. R. China.
Adv Healthc Mater. 2024 Nov;13(29):e2402342. doi: 10.1002/adhm.202402342. Epub 2024 Jul 19.
Current phototherapeutic approaches for Alzheimer's disease (AD) exhibit restricted clinical outcomes due to the limited physical penetration and comprised brain microenvironment of noninvasive nanomedicine. Herein, a hydrogen-bonded organic framework (HOF) based sonosensitizer is designed and synthesized. Mn-TCPP, a planar molecule where Mn ion is chelated in the core with a large p-conjugated system and 4 carboxylate acid groups, has been successfully used as building blocks to construct an ultrasound-sensitive HOF (USI-MHOF), which can go deep in the brain of AD animal models. The both in vitro and in vivo studies indicate that USI-MHOF can generate singlet oxygen (O) and oxidize β-amyloid (Aβ) to inhibit aggregation, consequently attenuating Aβ neurotoxicity. More intriguingly, USI-MHOF exhibits catalase (CAT)- and superoxide dismutase (SOD)-like activities, mitigating neuron oxidative stress and reprograming the brain microenvironment. For better crossing the blood-brain barrier (BBB), the peptide KLVFFAED (KD8) has been covalently grafted to USI-MHOF for improving BBB permeability and Aβ selectivity. Further, in vivo experiments demonstrate a significant reduction of the craniocerebral Aβ plaques and improvement of the cognition deficits in triple-transgenic AD (3×Tg-AD) mice models following deep-penetration ultrasound treatment. The work provides the first example of an ultrasound-responsive biocompatible HOF as non-invasive nanomedicine for in-depth treatment of AD.
目前用于阿尔茨海默病(AD)的光疗方法由于非侵入性纳米医学的有限物理穿透性和受限的脑微环境,临床效果有限。在此,设计并合成了基于氢键有机框架(HOF)的声敏剂。Mn-TCPP 是一种平面分子,其核心处的 Mn 离子与大的 p-共轭体系和 4 个羧酸盐基团螯合,已成功用作构建超声敏感 HOF(USI-MHOF)的构建块,该 HOF 可以深入到 AD 动物模型的大脑中。体外和体内研究均表明,USI-MHOF 可以产生单线态氧(O)并氧化β-淀粉样蛋白(Aβ)以抑制聚集,从而减轻 Aβ 神经毒性。更有趣的是,USI-MHOF 表现出过氧化氢酶(CAT)和超氧化物歧化酶(SOD)样活性,减轻神经元氧化应激并重新编程脑微环境。为了更好地穿透血脑屏障(BBB),将肽 KLVFFAED(KD8)共价接枝到 USI-MHOF 上,以提高 BBB 通透性和 Aβ 选择性。此外,体内实验表明,在深度穿透超声处理后,三转基因 AD(3×Tg-AD)小鼠模型的颅脑 Aβ 斑块显著减少,认知缺陷得到改善。这项工作提供了第一个超声响应性生物相容性 HOF 的例子,作为用于 AD 深度治疗的非侵入性纳米医学。