用炭黑和Ag/δ-FeOOH修饰一次性碳基电化学电池用于非酶催化H2O2电化学传感

Wiviane E. R. de Melo, Karoline S. Nantes, Ana L. H. K. Ferreira, Márcio C. Pereira, Luiz H. C. Mattoso, Ronaldo C. Faria, André S. Afonso
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引用次数: 0

摘要

过氧化氢(H2O2)是检测神经退行性疾病和炎症过程的重要分析物,在制药、食品工业和环境监测中起着至关重要的作用。然而,传统的H2O2检测方法存在分析时间长、成本高、设备笨重等缺点。非酶传感器已成为克服这些限制的有希望的替代品。在这项研究中,我们介绍了一种简单、便携、具有成本效益的非酶传感器,该传感器使用炭黑(CB)和银纳米颗粒修饰的δ-FeOOH (Ag/δ-FeOOH)集成到一次性电化学电池(DCell)中。扫描电镜(SEM)、能量色散x射线能谱(EDS)和电化学阻抗谱(EIS)证实了CB和Ag/δ-FeOOH在DCell工作电极上的成功固定。电化学研究表明,DCell-CB//Ag/δ-FeOOH传感器的表观非均相电子传递速率常数比DCell-Ag/δ-FeOOH传感器高约两倍,充分利用了CB的优势。此外,该传感器对H2O2还原具有良好的电化学响应,检测限低至22 μ M,分析灵敏度高至214 μA mM−1 cm−2。值得注意的是,DCell-CB//Ag/δ-FeOOH传感器对H2O2检测具有出色的选择性,即使在潜在的干扰物如多巴胺、尿酸和抗坏血酸中也是如此。此外,该传感器具有监测复杂生物样品中H2O2的良好品质,在10%的胎牛血清中H2O2的回收率为92%至103%。这些发现强调了DCell-CB//Ag/δ-FeOOH传感器在各种生物医学和环境应用中精确可靠地监测H2O2的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Disposable Carbon-Based Electrochemical Cell Modified with Carbon Black and Ag/δ-FeOOH for Non-Enzymatic H2O2 Electrochemical Sensing
Hydrogen peroxide (H2O2) is an essential analyte for detecting neurodegenerative diseases and inflammatory processes and plays a crucial role in pharmaceuticals, the food industry, and environmental monitoring. However, conventional H2O2 detection methods have drawbacks such as lengthy analysis times, high costs, and bulky equipment. Non-enzymatic sensors have emerged as promising alternatives to overcome these limitations. In this research, we introduce a simple, portable, and cost-effective non-enzymatic sensor that uses carbon black (CB) and silver nanoparticle-modified δ-FeOOH (Ag/δ-FeOOH) integrated into a disposable electrochemical cell (DCell). Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and electrochemical impedance spectroscopy (EIS) confirmed successful CB and Ag/δ-FeOOH immobilization on the DCell working electrode. Electrochemical investigations revealed that the DCell-CB//Ag/δ-FeOOH sensor exhibited an approximately twofold higher apparent heterogeneous electron transfer rate constant than the DCell-Ag/δ-FeOOH sensor, capitalizing on CB’s advantages. Moreover, the sensor displayed an excellent electrochemical response for H2O2 reduction, boasting a low detection limit of 22 µM and a high analytical sensitivity of 214 μA mM−1 cm−2. Notably, the DCell-CB//Ag/δ-FeOOH sensor exhibited outstanding selectivity for H2O2 detection, even in potential interferents such as dopamine, uric acid, and ascorbic acid. Furthermore, the sensor has the right qualities for monitoring H2O2 in complex biological samples, as evidenced by H2O2 recoveries ranging from 92% to 103% in 10% fetal bovine serum. These findings underscore the considerable potential of the DCell-CB//Ag/δ-FeOOH sensor for precise and reliable H2O2 monitoring in various biomedical and environmental applications.
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