Immobilization of 4-MBA & Cu2+on Au nanoparticles modified screen-printed electrode for glyphosate detection

被引:3
作者
Li, Wei [1 ,4 ]
Wu, Hongqi [1 ]
Wu, Cong [2 ,3 ]
Jiao, Peidong [1 ]
Xu, Ling [5 ]
Song, Haiyan [1 ,4 ]
机构
[1] Shanxi Agr Univ, Coll Agr Engn, Taigu 030801, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Urol, Chengdu 610041, Peoples R China
[3] Sichuan Univ, West China Hosp, Inst Syst Genet, Chengdu 610041, Peoples R China
[4] Dryland Farm Machinery Key Technol & Equipment Key, Taigu 030801, Peoples R China
[5] Shanxi Hongrunqing Environm Protect Technol Co Ltd, Taiyuan 030000, Peoples R China
关键词
4-Mercaptobenzoic acid (4-MBA); Electrochemical sensor; Self-assembled monolayer (SAM); Glyphosate; Square wave voltammetry (SWV); GOLD NANOPARTICLES; MONOLAYERS; BIOSENSOR; ACID;
D O I
10.1016/j.talanta.2025.127530
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This study introduces an innovative electrochemical biosensor, engineered through the functionalization screen- printed electrode (SPE) with a coordination complex comprised of 4-mercaptobenzoic acid (4-MBA) and copper ions (Cu2+), achieving precise quantitative determination of glyphosate. Electrodepositing gold nanoparticles (AuNPs) onto the electrode surface, forming a self-assembled monolayer (SAM) of 4-MBA via thiol-gold interactions, and immobilizing Cu2+ via coordination bonding with the monolayer, finalizing the electrochemical biosensor construction as Cu2+/4-MBA/AuNPs/SPE. The successful modification of the biosensor interface is confirmed through scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and electrochemical characterization. Through parameter optimization, critical metrics for the biosensor preparation process have been determined. Using square wave voltammetry (SWV), a linear relationship between the glyphosate concentration and the peak current inhibition ratio at the electrode surface is established. Additionally, the repeatability and anti-interference capabilities of the fabricated biosensors are evaluated. The experimental outcomes affirm the biosensor's capability for quantitative glyphosate detection across a 5-100 nM range, boasting a 1.65 nM limit of detection (LOD). Testing on tap water samples verifies a robust recovery rate for glyphosate residues, spanning 89.84 %-107.48 %. The proposed biosensor holds significant promise for glyphosate detection, offering substantial applicability and this study provides a valuable reference for the advancement of biosensors geared toward the quantitative assessment of organophosphate pesticides (OPs).
引用
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页数:11
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