胶体金
神经毒性
细胞毒性
淀粉样蛋白(真菌学)
化学
血脑屏障
阿尔茨海默病
纳米颗粒
纳米技术
药理学
体外
医学
材料科学
疾病
神经科学
生物化学
生物
毒性
中枢神经系统
病理
无机化学
有机化学
作者
Nan Gao,Hanjun Sun,Kai Dong,Jinsong Ren,Xiaogang Qu
标识
DOI:10.1002/chem.201404562
摘要
Abstract Targeting amyloid‐β (Aβ)‐induced complex neurotoxicity has received considerable attention in the therapeutic and preventive treatment of Alzheimer’s disease (AD). The complex pathogenesis of AD suggests that it requires comprehensive treatment, and drugs with multiple functions against AD are more desirable. Herein, AuNPs@POMD‐pep (AuNPs: gold nanoparticles, POMD: polyoxometalate with Wells–Dawson structure, pep: peptide) were designed as a novel multifunctional Aβ inhibitor. AuNPs@POMD‐pep shows synergistic effects in inhibiting Aβ aggregation, dissociating Aβ fibrils and decreasing Aβ‐mediated peroxidase activity and Aβ‐induced cytotoxicity. By taking advantage of AuNPs as vehicles that can cross the blood–brain barrier (BBB), AuNPs@POMD‐pep can cross the BBB and thus overcome the drawbacks of small‐molecule anti‐AD drugs. Thus, this work provides new insights into the design and synthesis of inorganic nanoparticles as multifunctional therapeutic agents for treatment of AD.
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