Ultrafast synthesized monometallic nanohybrids as an efficient quencher and recognition antenna of upconversion nanoparticles for the detection of xanthine with enhanced sensitivity and selectivity

化学 光子上转换 费斯特共振能量转移 检出限 纳米探针 荧光 猝灭(荧光) 纳米颗粒 纳米团簇 光化学 胶体金 纳米技术 组合化学 离子 材料科学 色谱法 光学 有机化学 物理
作者
Jie Chen,Haiyang Zheng,Wen Li,Qing‐Feng Li,Bin Hu,Nan‐Sim Pang,Fengshou Tian,Lin Jin
出处
期刊:Talanta [Elsevier BV]
卷期号:245: 123471-123471 被引量:9
标识
DOI:10.1016/j.talanta.2022.123471
摘要

Upconversion nanoparticles (UCNPs) have shown great promise in bioanalytical applications owing to their excellent optical properties. Generally, most analytical applications are based on the fluorescence resonance energy transfer (FRET) principle to quench the fluorescence of UCNPs. However, each UCNP contains thousands of emission center ions, and most of them exceed the FRET critical distance, which hinders FRET efficiency and leads to a low signal-to-background ratio (SBR). Herein, a novel nanoprobe for the detection of Xanthine (XA) based on inner filter effects (IFE) and cascade signal amplification strategy was constructed by decorating UCNP with trypsin-chymotrypsin-stabilized gold nanoparticles-gold nanoclusters (Try-chy-AuNPs-AuNCs) monometallic nanohybrids. The Try-chy-AuNPs-AuNCs prepared by ultrafast (3 min) and green synthesis method have efficient upconversion fluorescence quenching ability (the quenching efficiency up to 90.9%), which can effectively improve the SBR of the probe, so as to improve the sensitivity. In addition, the Try-chy-AuNPs-AuNCs have a unique spatial structure, which can effectively prevent the interaction between large-size biothiol (glutathione) and the probe, thus improving its selectivity. Besides, combined with the excellent optical performance of UCNPs and cascaded signal amplification strategy, the sensitivity of the probe can be further improved. Under the optimized conditions, the linear response range of the probe was obtained from 0.05 to 50 μM, 0.06-80 μM and with the low detection limit of 22.6 nM and 26.3 nM for H2O2 and XA, respectively. Meanwhile, the developed method has been further applied to the detection of XA in human serum with satisfactory results.
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