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基于具有高氧化酶活性的 Co-PBA 的荧光和比色法的简单无酶尿酸检测。

Simple enzyme-free detection of uric acid by an fluorescence and colorimetric method based on Co-PBA with high oxidase activity.

机构信息

State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin 541004, China.

出版信息

Analyst. 2024 Feb 26;149(5):1455-1463. doi: 10.1039/d3an01985c.


DOI:10.1039/d3an01985c
PMID:38190248
Abstract

In this work, we prepared a simple and low-cost cobalt-doped Prussian blue analog (Co-PBA), which can directly oxidize 10-acetyl-3,7-dihydroxyphenoxazine and 3,3',5,5'-tetramethylbenzidine (TMB) to produce resorufin (ox-AR) with high fluorescent quantum yield and ox-TMB with blue color, respectively, without the need for unstable HO. Using the Michaelis-Menten curve and Lineweaver-Burk equation, the Michaelis-Menten constant of Co-PBA and the substrate TMB was found to be 0.033 mM, which was much lower than horseradish peroxidase and other reported nanozymes, showing satisfactory substrate affinity. Uric acid (UA) can cause erosion of the Co-PBA structure, and it significantly reduces the catalytic activity of Co-PBA, resulting in the decrease of the fluorescence emission signal of ox-AR and the absorption signal of ox-TMB. Based on this, a simple, sensitive, and fast fluorescence/colorimetric dual-mode uric acid detection platform was established. The detection range for UA by fluorescence method is 0.625-40 μM, and the detection limit (LOD, S/N = 3) is as low as 0.389 μM. The detection system was applied to serum samples with good recovery and can be used for field detection of UA in biological samples under different environments to meet different needs.

摘要

在这项工作中,我们制备了一种简单且低成本的钴掺杂普鲁士蓝类似物(Co-PBA),它可以直接将 10-乙酰-3,7-二羟基吩恶嗪和 3,3',5,5'-四甲基联苯胺(TMB)氧化为具有高荧光量子产率的 Resorufin(ox-AR)和蓝色的 ox-TMB,而无需不稳定的 HO。通过 Michaelis-Menten 曲线和 Lineweaver-Burk 方程,发现 Co-PBA 和底物 TMB 的米氏常数为 0.033 mM,远低于辣根过氧化物酶和其他报道的纳米酶,表现出令人满意的底物亲和力。尿酸(UA)会侵蚀 Co-PBA 结构,显著降低 Co-PBA 的催化活性,导致 ox-AR 的荧光发射信号和 ox-TMB 的吸收信号降低。基于此,建立了一种简单、灵敏、快速的荧光/比色双模式尿酸检测平台。荧光法检测 UA 的线性范围为 0.625-40 μM,检测限(LOD,S/N = 3)低至 0.389 μM。该检测系统应用于血清样品中,具有良好的回收率,可用于不同环境下生物样品中 UA 的现场检测,以满足不同需求。

相似文献

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Simple enzyme-free detection of uric acid by an fluorescence and colorimetric method based on Co-PBA with high oxidase activity.

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