Reverse iontophoresis sensing electrode for joint detection of pH, NH4+, and lactic acid

IF 4.1 3区 化学 Q1 CHEMISTRY, ANALYTICAL Journal of Electroanalytical Chemistry Pub Date : 2024-10-16 DOI:10.1016/j.jelechem.2024.118722
Qiya Gao , Zetao Chen , Yongchang Bai , Jie Fu , Ziyue Qin , Shuang Li
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Abstract

With the rapid development of integrated electronic circuit technology, biological fluid-electricity integrated detection systems have gradually become a research hotspot. Researchers have integrated biological fluid electrical detection methods into circuits and developed small, low-power, portable detection devices equipped with sensing electrodes, which can achieve continuous monitoring of human health parameters. In recent years, the integration of reverse iontophoresis technology that can be used to extract body fluids with electrochemical sensors has opened up the possibility of flexible, portable biochemical sensing with excellent detection sensitivity. Herein, we present a method for extracting biofluids based on reverse iontophoresis technology, coupled with electrochemical sensing techniques for the simultaneous detection of various biomarkers in body fluids. The multi-channel sensing electrode was modified layer by layer using nitrogen-doped graphene (N-Gr), ion-selective membrane, or lactate oxidase for rapid and sensitive detection of pH (3–8), ammonium ion (NH4+) (0.1 mM–50 mM), and lactic acid (1 mM–50 mM). Subsequently, an integrated system for electrical stimulation extraction and sensing analysis based on reverse iontophoresis was established and experimentally tested. Experimental results demonstrated that the multi-channel joint detection sensing electrode has excellent sensing linearity, specificity, repeatability, and long-term stability. Finally, a smartphone-based WeChat applet was developed, which can realize parameter setting, function selection, and result display of sensor detection. In this study, reverse iontophoresis technology was used to collect body fluids, and the important biomarkers pH, NH4+, and lactic acid in the body fluids were detected. Overall, this research presents an integrated detection system and a multi-channel sensing scheme for the detection of important biochemical markers in bodily fluids, thereby providing potential value for health monitoring applications.
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用于联合检测 pH 值、NH4+ 和乳酸的反向离子渗透传感电极
随着集成电子电路技术的飞速发展,生物液电一体化检测系统逐渐成为研究热点。研究人员将生物液电检测方法集成到电路中,开发出了配备传感电极的小型、低功耗、便携式检测设备,可实现对人体健康参数的连续监测。近年来,可用于提取体液的反向离子电泳技术与电化学传感器的结合,为灵活、便携、检测灵敏度高的生化传感技术提供了可能。在此,我们介绍一种基于反向离子渗透技术的生物液体提取方法,该方法与电化学传感技术相结合,可同时检测体液中的各种生物标记物。利用掺氮石墨烯(N-Gr)、离子选择膜或乳酸氧化酶对多通道传感电极进行逐层修饰,可快速灵敏地检测 pH 值(3-8)、铵离子(NH4+)(0.1 mM-50 mM)和乳酸(1 mM-50 mM)。随后,建立了基于反向离子渗透的电刺激提取和传感分析集成系统,并进行了实验测试。实验结果表明,多通道关节检测传感电极具有良好的传感线性度、特异性、重复性和长期稳定性。最后,开发了基于智能手机的微信小程序,可实现传感检测的参数设置、功能选择和结果显示。本研究采用反向离子透入技术采集体液,检测了体液中重要的生物标志物 pH、NH4+ 和乳酸。总之,本研究提出了一种用于检测体液中重要生化标志物的集成检测系统和多通道传感方案,从而为健康监测应用提供了潜在价值。
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来源期刊
CiteScore
7.80
自引率
6.70%
发文量
912
审稿时长
2.4 months
期刊介绍: The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied. Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.
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