Chiral Skeletons of Mesoporous Silica Nanospheres to Mitigate Alzheimer’s β-Amyloid Aggregation

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2023-04-01 DOI:10.1021/jacs.2c12214
Li Xu, Min Guo, Chin-Te Hung, Xiao-Lei Shi, Yiwen Yuan, Xingmiao Zhang, Ren-Hua Jin, Wei Li, Qiang Dong* and Dongyuan Zhao*, 
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引用次数: 6

Abstract

Chiral mesoporous silica (mSiO2) nanomaterials have gained significant attention during the past two decades. Most of them show a topologically characteristic helix; however, little attention has been paid to the molecular-scale chirality of mSiO2 frameworks. Herein, we report a chiral amide-gel-directed synthesis strategy for the fabrication of chiral mSiO2 nanospheres with molecular-scale-like chirality in the silicate skeletons. The functionalization of micelles with the chiral amide gels via electrostatic interactions realizes the growth of molecular configuration chiral silica sols. Subsequent modular self-assembly results in the formation of dendritic large mesoporous silica nanospheres with molecular chirality of the silica frameworks. As a result, the resultant chiral mSiO2 nanospheres show abundant large mesopores (∼10.1 nm), high pore volumes (∼1.8 cm3·g–1), high surface areas (∼525 m2·g–1), and evident CD activity. The successful transfer of the chirality from the chiral amide gels to composited micelles and further to asymmetric silica polymeric frameworks based on modular self-assembly leads to the presence of molecular chirality in the final products. The chiral mSiO2 frameworks display a good chiral stability after a high-temperature calcination (even up to 1000 °C). The chiral mSiO2 can impart a notable decline in β-amyloid protein (Aβ42) aggregation formation up to 79%, leading to significant mitigation of Aβ42-induced cytotoxicity on the human neuroblastoma line SH-ST5Y cells in vitro. This finding opens a new avenue to construct the molecular chirality configuration in nanomaterials for optical and biomedical applications.

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介孔二氧化硅纳米球手性骨架减轻阿尔茨海默病β-淀粉样蛋白聚集
手性介孔二氧化硅(mSiO2)纳米材料在过去的二十年中得到了广泛的关注。它们大多具有拓扑特征的螺旋结构;然而,对二氧化硅骨架的分子尺度手性的研究却很少。本文报道了一种手性酰胺凝胶定向合成策略,用于在硅酸盐骨架中制备具有分子级手性的手性二氧化硅纳米球。通过静电相互作用,胶束与手性酰胺凝胶的功能化实现了分子构型手性硅溶胶的生长。随后的模块化自组装形成了具有分子手性的枝状大介孔二氧化硅纳米球。结果表明,所制得的手性二氧化硅纳米球具有丰富的大介孔(~ 10.1 nm)、高孔体积(~ 1.8 cm3·g-1)、高表面积(~ 525 m2·g-1)和明显的CD活性。手性从手性酰胺凝胶成功转移到复合胶束,并进一步转移到基于模块化自组装的不对称硅聚合物框架,导致最终产品中存在分子手性。手性二氧化硅骨架在高温煅烧(甚至高达1000℃)后显示出良好的手性稳定性。手性二氧化硅能显著降低β-淀粉样蛋白(a - β42)聚集形成达79%,从而显著减轻a - β42诱导的体外人神经母细胞瘤SH-ST5Y细胞的细胞毒性。这一发现为构建用于光学和生物医学应用的纳米材料中的分子手性构型开辟了一条新的途径。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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