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基于金纳米粒子在双氧水介导下的放大作用对内滤效应的尿酸荧光探针的研究。

Gold nanoclusters as switch-off fluorescent probe for detection of uric acid based on the inner filter effect of hydrogen peroxide-mediated enlargement of gold nanoparticles.

机构信息

Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research (Ministry of Education of China), Hunan Normal University, Changsha 410081, China.

Key Laboratory of Phytochemical R&D of Hunan Province, Hunan Normal University, Changsha 410081, China.

出版信息

Biosens Bioelectron. 2017 May 15;91:734-740. doi: 10.1016/j.bios.2017.01.020. Epub 2017 Jan 17.

DOI:10.1016/j.bios.2017.01.020
PMID:28130993
Abstract

Herein we report a novel switch-off fluorescent probe for highly selective determination of uric acid (UA) based on the inner filter effect (IFE), by using poly-(vinylpyrrolidone)-protected gold nanoparticles (PVP-AuNPs) and chondroitin sulfate-stabilized gold nanoclusters (CS-AuNCs) as the IFE absorber/fluorophore pair. In this IFE-based fluorometric assay, the newly designed CS-AuNCs were explored as an original fluorophore and the hydrogen peroxide (HO) -driven formed PVP-AuNPs can be a powerful absorber to influence the excitation of the fluorophore, due to the complementary overlap between the absorption band of PVP-AuNPs and the emission band of CS-AuNCs. Under the optimized conditions, the extent of the signal quenching depends linearly on the HO concentration in the range of 1-100μM (R =0.995) with a detection limit down to 0.3μM. Based on the HO-dependent fluorescence IFE principle, we further developed a new assay strategy to enable selective sensing of UA by using a specific uricase-catalyzed UA oxidation as the in situ HO generator. The proposed uricase-linked IFE-based assay exhibited excellent analytical performance for measuring UA over the concentration ranging from 5 to 100μM (R=0.991), and can be successfully applied to detection of UA as low as 1.7μM (3σ) in diluted human serum samples.

摘要

在此,我们报告了一种基于内滤效应(IFE)的新型关闭型荧光探针,用于高选择性测定尿酸(UA),该探针使用聚(聚乙烯吡咯烷酮)保护的金纳米粒子(PVP-AuNPs)和硫酸软骨素稳定的金纳米簇(CS-AuNCs)作为 IFE 吸收体/荧光团对。在这种基于 IFE 的荧光测定法中,新设计的 CS-AuNCs 被探索作为原始荧光团,而过氧化氢(HO)驱动形成的 PVP-AuNPs 可以作为强大的吸收体来影响荧光团的激发,这是由于 PVP-AuNPs 的吸收带和 CS-AuNCs 的发射带之间的互补重叠。在优化条件下,信号猝灭的程度与 HO 浓度在 1-100μM 范围内呈线性关系(R =0.995),检测限低至 0.3μM。基于 HO 依赖性荧光 IFE 原理,我们进一步开发了一种新的测定策略,通过使用特定的尿酸酶催化的 UA 氧化作为原位 HO 发生器,实现 UA 的选择性检测。所提出的与尿酸酶相关的基于 IFE 的测定法在 5 至 100μM(R=0.991)的浓度范围内对 UA 的测定表现出优异的分析性能,并且可以成功地应用于在稀释的人血清样品中检测低至 1.7μM(3σ)的 UA。

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