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