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一种基于具有增强过氧化物酶样活性的碳点纳米酶的用于检测D-氨基酸的超灵敏比色/荧光/光热传感平台。

An ultrasensitive colorimetric/fluorescent/photothermal sensing platform for the detection of D-amino acids based on carbon dots nanozymes with enhanced peroxidase-like activity.

作者信息

Wu Wei, Ni Chen, Huang Yan-Li, Cheng Hui-Ling, Shi Yu-Han, Zhang Ya-Hui, Xu Zhi-Hong, Zhang Guo-Qi

机构信息

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

Asymmetric Synthesis and Chiral Technology Key Laboratory of Sichuan Province, Xihua University, Chengdu, 610039, PR China.

出版信息

Mikrochim Acta. 2025 Jan 20;192(2):95. doi: 10.1007/s00604-025-06961-0.

Abstract

Based on the enhanced peroxidase-like activity of carbon dots nanozymes (CDszymes), with a specific oxidation reaction of D-amino acid oxidase catalysing the formation of HO from D-amino acid, an ultrasensitive sensing platform, was constructed for the quantitative detection of D-amino acids in saliva. With the increase of D-amino acids concentration, the blue color of catalytic product gradually deepend, the fluorescence CDszymes gradually quenched, and the temperature gradually increased. Using D-alanine as D-amino acid models, the detection limits of D-alanine in colorimetric/photothermal/fluorescent mode were 0.3 μM, 1.8 μM, and 0.04 μM, respectively. The proposed detection platform exhibits promising application potential in clinical diagnostics. The exceptional sensing performance can be attributed to the utilization of CDszymes with outstanding POD activity. Revolving around the blind synthesis of CDszymes exhibiting high-efficiency POD activity, this study delved into the underlying mechanism governing the regulation of the POD activity of CDszymes by precursor functional groups. This work investigates the valence band theory to enhance the peroxidase-like of CDszymes, thereby offering a rational approach for designing CDszymes.

摘要

基于碳点纳米酶(CD酶)增强的过氧化物酶样活性,利用D-氨基酸氧化酶催化D-氨基酸形成H₂O₂的特定氧化反应,构建了一种用于定量检测唾液中D-氨基酸的超灵敏传感平台。随着D-氨基酸浓度的增加,催化产物的蓝色逐渐加深,荧光CD酶逐渐猝灭,温度逐渐升高。以D-丙氨酸作为D-氨基酸模型,比色/光热/荧光模式下D-丙氨酸的检测限分别为0.3 μM、1.8 μM和0.04 μM。所提出的检测平台在临床诊断中具有广阔的应用潜力。这种优异的传感性能可归因于对具有出色过氧化物酶(POD)活性的CD酶的利用。围绕具有高效POD活性的CD酶的盲目合成,本研究深入探讨了前体官能团调控CD酶POD活性的潜在机制。这项工作研究了价带理论以增强CD酶的过氧化物酶样活性,从而为设计CD酶提供了一种合理的方法。

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