Synergistic recognition and electrochemical sensing of 17β-Estradiol using ordered molecularly imprinted polymer-graphene oxide-silver nanoparticles composite films

Abstract

Synthetic molecularly imprinted polymers (MIPs) based functional materials become the best alternatives to alleviate the stability and cost issues related to biological receptors commonly used in biochemical sensors. To address this demand, we report the development of a highly selective and sensitive MIPs-based electrochemical sensor for the detection of 17β-estradiol (E2). The sensor was prepared based on the MIP-graphene oxide (GO)-silver nanoparticle (AgNP) nanocomposite functional materials electrodeposited on the surface of the glassy carbon electrode (GCE). At first, AgNp formation was facilitated by using ascorbic acid to reduce and stabilize it. A very stable MIP-GO-AgNP sensing layer with multifunctional units were formed using imidazole as a functional monomer (p-type-electron acceptor), GO (n-type-electron donor), and AgNP by using the electrodeposition method. The role of GO in the system is providing additional functional units to bind the template and improve materials morphology while that of AgNPs is acting as a catalyst and charge carrier. The characterization of the sensing materials was done by using Fourier transform infrared, scanning electron microscopy, energy dispersive X-ray spectroscopy, and cyclic voltammetry. After optimization of the essential parameters, the sensor was successfully applied to detect the target analyte using the square wave voltammetric technique. The prepared sensor exhibited a wide linear range of 10 fM-250 nM with the limit of detection and limit of quantification of 3.01 fM and 10.03 fM, respectively. The high percentage recoveries, sensitivity, repeatability, and easy fabrication of the MIP-GO-AgNP materials made the proposed sensor promising for environmental monitoring applications in the future.