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Gold-Nanoparticle-Based Multifunctional Amyloid-beta Inhibitor against Alzheimer's Disease

机译:基于金纳米粒子的多功能淀粉样β抑制剂对阿尔茨海默氏病

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摘要

Targeting amyloid-beta (A beta)-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 A beta inhibitor. AuNPs@POMD-pep shows synergistic effects in inhibiting A beta aggregation, dissociating A beta fibrils and decreasing A beta-mediated peroxidase activity and A beta-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.
机译:靶向淀粉样β(A beta)诱导的复杂神经毒性在阿尔茨海默氏病(AD)的治疗和预防性治疗中受到了相当大的关注。 AD的复杂发病机制表明它需要综合治疗,并且更需要具有多种抗AD功能的药物。在此,将AuNPs @ POMD-pep(AuNPs:金纳米颗粒,POMD:具有Wells-Dawson结构的多金属氧酸盐,pep:肽)设计为新型多功能Aβ抑制剂。 AuNPs @ POMD-pep在抑制Aβ聚集,解离Aβ原纤维和降低Aβ介导的过氧化物酶活性和Aβ诱导的细胞毒性方面显示出协同作用。通过利用AuNPs作为可以穿越血脑屏障(BBB)的媒介,AuNPs @ POMD-pep可以穿越BBB,从而克服了小分子抗AD药物的缺点。因此,这项工作为无机纳米颗粒的设计和合成提供了新的见解,作为治疗AD的多功能治疗剂。

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