The
extensive use of the herbicide glyphosate has raised several
health concerns due to the known toxicity of this chemical. The existing
methods for glyphosate detection need better and more rapid accessibility
for quick detection in an efficient manner. Here, we report an ultrasensitive
aptamer-based electrochemical detection method for glyphosate. A high
affinity single-stranded DNA (ssDNA) that binds specifically to glyphosate
(GlyP) was selected and identified in vitro by the method of systemic
evolution of ligands by exponential enrichment (SELEX) assisted by
graphene oxide (GO), GO-SELEX. After eight GO-SELEX cycles, the ssDNA
was sequenced, and the obtained aptamers were subjected to binding
assays to evaluate their affinity and specificity to GlyP. The inherent
GlyP–aptamer interaction was investigated by circular dichroism
spectroscopy (CD). The selected sequence, denominated GlyP_1, exhibited
a low dissociation constant (K
d) of 30.73
± 1.25 nM and excellent selectivity for glyphosate. Prior to
gold electrode modification, GlyP_1 was functionalized by the disulfide
label and used as a recognition element for glyphosate detection.
The surface modification steps for the gold electrodes to develop
the aptasensor were followed up by cyclic voltammetry (CV) and electrochemical
impedance spectroscopy (EIS) in the presence of a redox probe, [Fe(CN)6]3–/4–. The resulting aptasensor
demonstrated an operation range from 1.16 pM to 400 pM, with a limit
of detection (LOD) of 1.16 pM. Thus, in this work we report an effective
sensing method that could provide a potential alternative to traditional
analyses techniques for quick and easy monitoring of glyphosate in
food and water.