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基于酶诱导形成有色 Au@Ag 纳米粒子和内滤效应的荧光和比色双读数碱性磷酸酶活性测定法。

Fluorometric and colorimetric dual-readout alkaline phosphatase activity assay based on enzymatically induced formation of colored Au@Ag nanoparticles and an inner filter effect.

机构信息

School of Materials Science and Engineering, University of Jinan, Jinan, 250022, China.

College of Chemistry, Chemical Engineering and Materials Science, Key Laboratory of Molecular and Nano Probes (Ministry of Education), Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Institute of Molecular and Nano Science, Shandong Normal University, Jinan, 250014, China.

出版信息

Mikrochim Acta. 2019 May 11;186(6):348. doi: 10.1007/s00604-019-3478-6.

Abstract

An ultrasensitive fluorometric and colorimetric dual-mode assay is described for the determination of the activity of alkaline phosphatase (ALP). ALP catalyzes the decomposition of 2-phospho-L-ascorbic acid, and the ascorbic acid thus generated reduces silver ions. In the presence of gold nanoparticles, gold-silver nanoparticles (Au@Ag NPs) are formed. This is accompanied by a color change form pink to deep yellow. The Au@Ag NPs reduce the fluorescence of blue fluorescent graphene quantum dots due to spectral overlap. The changes of absorbance (measured at 410 and 520 nm) and fluorescence (measured at excitation/emission wavelengths of 346/415 nm) correlate well with the ALP activity in the 0.01-6 mU·mL (absorption) and 0.01-2 mU·mL (fluorescence) ranges, and the detection limits are 9 and 5 μU·mL individually. Graphical abstract Schematic presentation of colorimetric and fluorometric dual-readout assay for alkaline phosphatase (ALP) activity. It is based on enzymatically induced formation of gold-silver nanoparticles (Au@Ag NPs), and the fluorescence quenching of graphene quantum dots due to inner filter effect.

摘要

一种用于测定碱性磷酸酶(ALP)活性的超灵敏荧光和比色双模式分析方法。ALP 催化 2-磷酸-L-抗坏血酸的分解,生成的抗坏血酸还原银离子。在金纳米粒子存在下,形成金-银纳米粒子(Au@Ag NPs)。这伴随着颜色从粉红色变为深黄色的变化。Au@Ag NPs 由于光谱重叠而使蓝色荧光石墨烯量子点的荧光降低。吸光度(在 410 和 520nm 处测量)和荧光(在 346/415nm 的激发/发射波长处测量)的变化与 0.01-6mU·mL(吸收)和 0.01-2mU·mL(荧光)范围内的 ALP 活性很好地相关,检测限分别为 9 和 5μU·mL。

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