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<p> A&#xa0;novel electrochemical sensor&#xa0;is introduced that significantly accelerates sialic acid (SA) detection by utilizing an electrophoresis device, which reduces the binding time from 20 to 5&#xa0;min. The results indicate that the current signal change (ΔI) of the sensor is more than twofold higher than that of conventional sensors after 5&#xa0;min. Furthermore, to enhance the intensity of the sensor’s signal and simplify the operational procedure, we employed a method that electrochemically reduces graphene oxide/3-aminophenylboronic acid (GO/APBA) to reduced graphene oxide/3-aminophenylboronic acid (rGO/APBA) in a single step. This reduction process effectively removes some oxygen groups from GO, further enhancing the current signal. The linear detection range for SA was between 0.1&#xa0;mM and 3&#xa0;mM, with a detection limit of 0.084&#xa0;mM (S/N = 3). Notably, the electrophoresis-enhanced sensor can successfully detect SA in actual human serum samples. Overall, this sensor represents a significant advancement in the electrochemical sensing of SA, providing a rapid, selective, and cost-effective approach for developing electric field-enhanced detection technologies.</p> Graphical Abstract <p></p>

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Electrophoresis-based electrochemical sensor for rapid detection of sialic acid in human serum

  • 期刊论文

  • 发表日期：

    2025年10月4日

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  • Xiaoqing Ming,
  • Zhanghong Wu,
  • Shuluo Yin,
  • Xiangyu Zuo,
  • Qing Lu,
  • Xiaoting Wu,
  • Xinhang Li,
  • Shengnan Tang,
  • Fangxin Liu,
  • Yuanfang Hou,
  • Jianjun Hu,
  • Guangchao Zang

摘要

A novel electrochemical sensor is introduced that significantly accelerates sialic acid (SA) detection by utilizing an electrophoresis device, which reduces the binding time from 20 to 5 min. The results indicate that the current signal change (ΔI) of the sensor is more than twofold higher than that of conventional sensors after 5 min. Furthermore, to enhance the intensity of the sensor’s signal and simplify the operational procedure, we employed a method that electrochemically reduces graphene oxide/3-aminophenylboronic acid (GO/APBA) to reduced graphene oxide/3-aminophenylboronic acid (rGO/APBA) in a single step. This reduction process effectively removes some oxygen groups from GO, further enhancing the current signal. The linear detection range for SA was between 0.1 mM and 3 mM, with a detection limit of 0.084 mM (S/N = 3). Notably, the electrophoresis-enhanced sensor can successfully detect SA in actual human serum samples. Overall, this sensor represents a significant advancement in the electrochemical sensing of SA, providing a rapid, selective, and cost-effective approach for developing electric field-enhanced detection technologies.

Graphical Abstract