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基于生物无机级联反应,Mn 掺杂 CeO 纳米粒子具有增强的过氧化物酶样活性,可在中性 pH 条件下用于葡萄糖的一锅分析。

The Mn-doped CeO nanoparticles with enhanced peroxidase-like activity for one-pot analysis of glucose at neutral pH based on bio-inorganic cascade reactions.

机构信息

College of Chemistry, Institute of Analytical Chemistry for Life Science, Food Laboratory of Zhongyuan, Zhengzhou University, Zhengzhou, 450001, PR China.

College of Chemistry, Institute of Analytical Chemistry for Life Science, Food Laboratory of Zhongyuan, Zhengzhou University, Zhengzhou, 450001, PR China.

出版信息

Talanta. 2024 Nov 1;279:126603. doi: 10.1016/j.talanta.2024.126603. Epub 2024 Jul 22.

Abstract

Enzyme catalytic cascade reactions based on peroxidase nanozymes and natural enzymes have aroused extensive attention in analytical fields. However, a majority of peroxidase nanozymes perform well only in acidic environments, resulting in their optimal pH mismatch with a neutral pH of natural enzymes, further restricting their application in biochemical sensing. Herein, Mn-doped CeO (Mn/CeO) performing enhanced peroxidase-like activity at neutral conditions was prepared via a facile and feasible strategy. An effective enzyme cascade catalysis system via integrating glucose oxidase (GOx) with Mn/CeO was developed for one-pot detection of glucose in serum at neutral conditions. Using one-pot multistep catalytic reactions, this work provided a detection platform that allows for faster detection and easier operations than traditional methods. Under optimized conditions, our assay performed a sensitive detection of glucose ranging from 2.0 μΜ to 300 μΜ and a low detection limit of 0.279 μΜ. Notably, favorable analytical outcomes for glucose detection in serum samples were obtained, exhibiting potential applications in clinical diagnosis.

摘要

基于过氧化物酶纳米酶和天然酶的酶催化级联反应在分析领域引起了广泛关注。然而,大多数过氧化物酶纳米酶仅在酸性环境下表现良好,导致其最佳 pH 值与天然酶的中性 pH 值不匹配,进一步限制了它们在生物化学传感中的应用。在此,通过一种简单可行的策略制备了在中性条件下表现出增强过氧化物酶样活性的 Mn 掺杂 CeO(Mn/CeO)。通过将葡萄糖氧化酶(GOx)与 Mn/CeO 集成,开发了一种有效的酶级联催化系统,用于在中性条件下一次性检测血清中的葡萄糖。通过一步多步催化反应,该工作提供了一个检测平台,与传统方法相比,该平台具有更快的检测速度和更简单的操作。在优化条件下,我们的测定法对葡萄糖的检测范围为 2.0 μΜ 至 300 μΜ,检测限低至 0.279 μΜ。值得注意的是,该方法在血清样品中葡萄糖检测方面获得了良好的分析结果,显示出在临床诊断中的潜在应用。

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