Heterostructure of Metal Oxides Integrated on a GCE for Estimation of H2O2 Capacity in Milk and Fruit Juice Samples

B. Silwana, M. Matoetoe
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引用次数: 0

Abstract

High levels of H2O2 in food can lead to oxidative stress. Which has been linked to a number of neurological diseases. Hence, its detection in beverages is essential. However, a complicated structure of the reaction medium of H2O2 makes the detection procedure very difficult. For this reason, sensitive strategic methods are required. In this study, quantification of H2O2 in milk and apple juice has been obtained via the electrochemical sensing platform based on GCE/SiO-CeONPs. Scanning Electron Microscopy (SEM), Cyclic voltammetry(CV), and electron impedance spectroscopy(EIS) were employed to characterize the composite. The kinetics investigation of the sensor with H2O2 revealed an a quasi-reversible one -electron adsorption process. Under optimized conditions, the Differential Pulse Voltammetry (DPV) in 0.1 M Phosphate buffer (PB) pH 5.5 of the H2O2 displayed a peak at 0.13 V vs. Ag/AgCl with the detection limits of 0.0004 µM, linearity range of 0.01–0.08 µM. The observed LOD values of this method for real samples were calculated to be 0.006 µM and 0.007 µM with LOQ of 0.02 µM for milk and apple juice, respectively. The recovery of the analyte was from 92 to 99%. Furthermore, due to good selectivity and stability, the benefit of this sensor is its applicability in multiple fields.
金属氧化物异质结构在GCE上的集成用于估计牛奶和果汁样品中的H2O2容量
食物中高浓度的H2O2会导致氧化应激。这与许多神经系统疾病有关。因此,在饮料中检测它是必要的。但由于H2O2反应介质结构复杂,使得检测过程非常困难。为此,需要采取敏感的战略方法。本研究通过基于GCE/SiO-CeONPs的电化学传感平台,实现了牛奶和苹果汁中H2O2的定量测定。利用扫描电镜(SEM)、循环伏安法(CV)和电子阻抗谱(EIS)对复合材料进行了表征。对传感器吸附H2O2的动力学研究表明,传感器吸附过程为准可逆的单电子吸附过程。在优化条件下,在0.1 M磷酸盐缓冲液(PB) pH为5.5的H2O2中,差分脉冲伏安法(DPV)对Ag/AgCl的检出限为0.0004µM,线性范围为0.01 ~ 0.08µM。计算出该方法对实际样品的LOD值分别为0.006µM和0.007µM,对牛奶和苹果汁的LOQ值分别为0.02µM。分析物的回收率为92% ~ 99%。此外,由于该传感器具有良好的选择性和稳定性,其优点是可应用于多个领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.30
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0.00%
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