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

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).