通过葡萄糖氧化酶-铜离子络合物的一步级联方法,用于使用便携式装置检测葡萄糖

IF 2.6 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Qingxi Wu, Hongxuan Zhang, Li Fu, Li Jia
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引用次数: 0

摘要

本研究基于葡萄糖氧化酶-铜离子配合物(GOx@Cu2+),建立了一步级联荧光检测蜂蜜中葡萄糖的方法。这些复合物表现出双重酶活性——葡萄糖氧化酶和过氧化物酶样活性——这使它们能够催化级联反应。该反应涉及葡萄糖和邻苯二胺(OPD)的氧化,导致形成2,3-二氨基吩嗪(oxOPD),这是一种具有荧光特性的化合物。该方法克服了酶之间pH不匹配的挑战,简化了检测过程,无需制备纳米材料,将检测时间缩短至20 min。通过对3种蜂蜜样品的分析,验证了该方法的可行性,回收率在96.4% ~ 106%之间,相对标准偏差小于1.9%。用毛细管电泳对三种蜂蜜样品进行了选择性和准确性验证。此外,还介绍了一种自行设计的便携式设备,可实现现场葡萄糖检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

One-step cascade method via glucose oxidase-copper ion complex for detecting glucose using a portable device

One-step cascade method via glucose oxidase-copper ion complex for detecting glucose using a portable device
In this study, a one-step cascade fluorescence method was developed for the detection of glucose in honey, based on the glucose oxidase-copper ion complexes (GOx@Cu2+). These complexes exhibit dual enzymatic activities—glucose oxidase and peroxidase-like activities—which enable them to catalyze a cascade reaction. This reaction involves the oxidation of glucose and o-phenylenediamine (OPD), leading to the formation of 2,3-diaminophenazine (oxOPD), a compound with fluorescent properties. The proposed method overcomes the challenges of pH mismatch between enzymes and streamlines the testing process, eliminating the need for nanomaterial preparation and reducing the detection time to just 20 min. The feasibility of the method was validated by analyzing three honey samples, achieving recoveries between 96.4 % and 106 %, with relative standard deviations of less than 1.9 %. The selectivity and accuracy of the method were verified by capillary electrophoresis in three honey samples. Moreover, a self-designed portable device was introduced to enable on-site glucose detection.
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来源期刊
Analytical biochemistry
Analytical biochemistry 生物-分析化学
CiteScore
5.70
自引率
0.00%
发文量
283
审稿时长
44 days
期刊介绍: The journal''s title Analytical Biochemistry: Methods in the Biological Sciences declares its broad scope: methods for the basic biological sciences that include biochemistry, molecular genetics, cell biology, proteomics, immunology, bioinformatics and wherever the frontiers of research take the field. The emphasis is on methods from the strictly analytical to the more preparative that would include novel approaches to protein purification as well as improvements in cell and organ culture. The actual techniques are equally inclusive ranging from aptamers to zymology. The journal has been particularly active in: -Analytical techniques for biological molecules- Aptamer selection and utilization- Biosensors- Chromatography- Cloning, sequencing and mutagenesis- Electrochemical methods- Electrophoresis- Enzyme characterization methods- Immunological approaches- Mass spectrometry of proteins and nucleic acids- Metabolomics- Nano level techniques- Optical spectroscopy in all its forms. The journal is reluctant to include most drug and strictly clinical studies as there are more suitable publication platforms for these types of papers.
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