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基于 Ag@SiO@SiO-RuBpy 复合纳米粒子的金属增强荧光的前列腺特异抗原靶触发信号开启检测。

Target-triggered signal turn-on detection of prostate specific antigen based on metal-enhanced fluorescence of Ag@SiO@SiO-RuBpy composite nanoparticles.

出版信息

Nanotechnology. 2017 Feb 10;28(6):065501. doi: 10.1088/1361-6528/28/6/065501. Epub 2017 Jan 3.

Abstract

A three-layer core-shell nanostructure consisting of a silver core, a silica spacer, and a fluorescent dye RuBpy-doped outer silica layer was fabricated, and the optimal metal-enhanced fluorescence (MEF) distance was explored through adjusting the thickness of the silica spacer. The results show that the optimal distance is ∼10.4 nm with the maximum fluorescence enhancement factor 2.12. Then a new target-triggered MEF 'turn-on' strategy based on the optimized composite nanoparticles was successfully constructed for quantitative detection of prostate specific antigen (PSA), by using RuBpy as the energy donor and BHQ-2 as the acceptor. The hybridization of the complementary DNA of PSA-aptamer immobilized on the surface of the MEF nanoparticles with PSA-aptamer modified with BHQ-2, brought BHQ-2 in close proximity to RuBpy-doped silica shell and resulted in the decrease of fluorescence. In the presence of target PSA molecules, the BHQ-PSA aptamer is dissociated from the surface of the nanoparticles with the fluorescence switched on. Therefore, the assay of PSA was achieved by measuring the varying fluorescence intensity. The results show that PSA can be detected in the range of 1-100 ng ml with a detection limit of 0.20 ng ml (6.1 pM), which is 6.7-fold increase of that using hollow RuBpy-doped silica nanoparticles. Moreover, satisfactory results were obtained when PSA was detected in 1% serum.

摘要

制备了一种由银核、二氧化硅间隔层和荧光染料 RuBpy 掺杂的外层二氧化硅壳组成的三层核壳纳米结构,并通过调节二氧化硅间隔层的厚度来探索最佳的金属增强荧光(MEF)距离。结果表明,最佳距离约为 10.4nm,最大荧光增强因子为 2.12。然后,基于优化的复合纳米粒子,成功构建了一种新的靶触发 MEF“开启”策略,用于前列腺特异性抗原(PSA)的定量检测,以 RuBpy 作为能量供体,BHQ-2 作为受体。与表面固定 MEF 纳米粒子的 PSA-适配体杂交的 PSA-适配体互补 DNA与用 BHQ-2 修饰的 PSA-适配体结合,使 BHQ-2 接近 RuBpy 掺杂的二氧化硅壳,导致荧光强度降低。在存在靶 PSA 分子的情况下,BHQ-PSA 适配体从纳米粒子表面解离,荧光开启。因此,通过测量荧光强度的变化来实现 PSA 的测定。结果表明,PSA 可以在 1-100ngml 的范围内检测到,检测限为 0.20ngml(6.1pM),这是使用空心 RuBpy 掺杂二氧化硅纳米粒子的 6.7 倍。此外,当在 1%血清中检测 PSA 时,得到了令人满意的结果。

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