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非热解合成类漆酶铁基单原子纳米酶用于高效双通道比色和荧光检测肾上腺素。

Non-pyrolytic synthesis of laccase-like iron based single-atom nanozymes for highly efficient dual-mode colorimetric and fluorescence detection of epinephrine.

机构信息

Department of Chemisty, School of Science, Xihua University, Chengdu, 610039, PR China.

Department of Chemisty, School of Science, Xihua University, Chengdu, 610039, PR China.

出版信息

Anal Chim Acta. 2024 Sep 15;1322:343031. doi: 10.1016/j.aca.2024.343031. Epub 2024 Jul 26.

DOI:10.1016/j.aca.2024.343031
PMID:39182985
Abstract

Single-atom nanozymes have garnered significant attention due to their exceptional atom utilization and ability to establish well-defined structure-activity relationships. However, conventional pyrolytic synthesis methods pose challenges such as high energy consumption and random local environments at the active sites, while achieving non-pyrolytic synthesis of single-atom nanozymes remains a formidable technical hurdle. The present study focuses on the synthesis of laccase-like iron-based single-atom nanozymes (Fe-SAzymes) using a non-pyrolysis method facilitated by microwave irradiation. Under low iron loading conditions, Fe-SAzymes exhibited significantly enhanced laccase activity (12.1 U/mg), surpassing that of laccase by 24-fold. Moreover, Fe-SAzymes demonstrated efficient catalytic oxidation of epinephrine (EP), enabling its colorimetric detection. Owing to the remarkable laccase activity of Fe-SAzymes, the conventional nanozymes EP detection time was reduced from 60 min to 20 min, with an impressive low detection limit as low as 2.95 μM. In addition, an ultra-sensitive fluorescence method for EP detection was developed using the internal filter effect of EP oxidation products and CDs combined with carbon dots probe. The detection limit of fluorescence method was only 0.39 μM. Therefore, an visual, fast, and highly sensitive dual-mode EP detection strategy has great potential in the clinical diagnostic industry.

摘要

单原子纳米酶由于其出色的原子利用率和能够建立明确的结构-活性关系而受到广泛关注。然而,传统的热解合成方法存在一些挑战,例如高能耗和活性位点的随机局部环境,而实现单原子纳米酶的非热解合成仍然是一个艰巨的技术难题。本研究聚焦于使用微波辐射辅助的非热解方法合成漆酶样铁基单原子纳米酶(Fe-SAzymes)。在低铁负载条件下,Fe-SAzymes 表现出显著增强的漆酶活性(12.1 U/mg),是漆酶的 24 倍。此外,Fe-SAzymes 能够有效催化肾上腺素(EP)的氧化,实现其比色检测。由于 Fe-SAzymes 具有出色的漆酶活性,传统的纳米酶 EP 检测时间从 60 分钟缩短至 20 分钟,检测限低至 2.95 μM。此外,还开发了一种基于 EP 氧化产物和 CDs 的内滤效应以及碳点探针的超灵敏荧光法用于 EP 检测。荧光法的检测限低至 0.39 μM。因此,这种可视化、快速和高灵敏度的双模式 EP 检测策略在临床诊断行业具有巨大的应用潜力。

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