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谷胱甘肽稳定的铜纳米簇介导的内滤效应用于灵敏和选择性测定对硝基苯酚和碱性磷酸酶活性。

Glutathione-stabilized copper nanoclusters mediated-inner filter effect for sensitive and selective determination of p-nitrophenol and alkaline phosphatase activity.

机构信息

College of Chemistry and Chemical Engineering, Institute for Conservation and Utilization of Agro-bioresources in Dabie Mountains, Xinyang Key Laboratory of Functional Nanomaterials for Bioanalysis, Xinyang Normal University, Xinyang 464000, China.

College of Chemistry and Chemical Engineering, Institute for Conservation and Utilization of Agro-bioresources in Dabie Mountains, Xinyang Key Laboratory of Functional Nanomaterials for Bioanalysis, Xinyang Normal University, Xinyang 464000, China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2022 Apr 15;271:120948. doi: 10.1016/j.saa.2022.120948. Epub 2022 Jan 25.

Abstract

A simple and highly selective fluorescence biosensor has been exploited for p-nitrophenol (p-NP) and alkaline phosphatase (ALP) activity detection based on the glutathione-stabilized copper nanoclusters (GSH-CuNCs) mediated-inner filter effect (IFE). The GSH-CuNCs were prepared by employing GSH as stabilizer and ascorbic acid (AA) as reductant. The obtained GSH-CuNCs exhibited a strong blue fluorescence emission at 420 nm with an excitation wavelength of 365 nm, which overlapped largely with the absorption spectra of p-nitrophenol (p-NP). Therefore, the luminescence of GSH-CuNCs could be quenched by p-NP through inner filter effect. In addition, ALP catalyzed the substrate p-nitrophenyl phosphate (p-NPP) to form p-nitrophenol (p-NP), which also leading to the fluorescence quenching of GSH-CuNCs. The fluorescent strategy was realized for the sensitive determination of p-NP and ALP activity with the promising limit of detection of 20 nM (for p-NP) and 0.003 mU⋅mL (for ALP). Furthermore, the method could be applied to detect the p-NP content in river water samples and ALP activity in human serum samples.

摘要

一种简单且高选择性的荧光生物传感器已被开发出来,用于基于谷胱甘肽稳定的铜纳米簇(GSH-CuNCs)介导的内滤效应(IFE)检测对硝基苯酚(p-NP)和碱性磷酸酶(ALP)的活性。GSH-CuNCs 是通过使用 GSH 作为稳定剂和抗坏血酸(AA)作为还原剂来制备的。所得的 GSH-CuNCs 在 420nm 处具有强烈的蓝色荧光发射,激发波长为 365nm,与对硝基苯酚(p-NP)的吸收光谱有很大重叠。因此,p-NP 通过内滤效应可以猝灭 GSH-CuNCs 的发光。此外,ALP 催化底物对硝基苯磷酸酯(p-NPP)形成对硝基苯酚(p-NP),这也导致 GSH-CuNCs 的荧光猝灭。该荧光策略已被用于灵敏检测 p-NP 和 ALP 活性,具有有希望的检测限为 20nM(p-NP)和 0.003mU·mL(ALP)。此外,该方法可用于检测河水样品中的 p-NP 含量和人血清样品中的 ALP 活性。

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