Novel graphene electrochemical transistors incorporating zirconia inorganic molecular imprinted layer:Design, construction and application for highly sensitive and selective detection of acetaminophen

Owing to their intrinsic amplifying effect together with chemical stability, graphene electrochemical transistor sensors (GECTs) are gaining momentum for sensing applications. However, the surface of GECTs for different detection substances must be modified with different recognition molecules, which was cumbersome and lack a universal method. Molecularly imprinted polymer (MIP) is a kind of polymer with specific recognition function for given molecules. Here, MIP and GECTs were combined to effectively solve the problem of weak selectivity of GECTs, and achieve the high sensitivity and selectivity of MIP-GECTs equipment in detecting acetaminophen (AP) in complex urine environment. A novel molecular imprinting sensor based on Au nanoparticles modified zirconia (ZrO2) inorganic molecular imprinting membrane on reduced graphene oxide (ZrO2-MIP-Au/rGO) was proposed. ZrO2-MIP-Au/rGO was synthesized by one-step electropolymerization using AP as template, ZrO2 precursor as the functional monomer. The -OH group on ZrO2 and the -OH/-CONH- group on AP were easily bonded by hydrogen bonding to form a MIP layer on the surface, which allows the sensor to have a large number of imprinted cavities for AP specific adsorption. As a proof of method, the GECTs based on ZrO2-MIP-Au/rGO functional gate electrode has the characteristics of wide linear range (0.1 nM-4 mM), low detection limit (0.1 nM) and high selectivity for AP detection. These achievements highlight the introduction of specific and selective MIP to GECTs with unique amplification function, which could effectively solve the problem of selectivity of GECTs in complex environments, suggesting the potential of MIP-GECTs in real-time diagnosis.

Automated summary

This article introduces a graphene electrochemical transistor sensor (GECTs) based on molecularly imprinted polymer (MIP). By combining MIP with GECTs, the problem of weak selectivity of GECTs is effectively solved, and high sensitivity and selectivity in detecting acetaminophen (AP) in complex urine environment are achieved.