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A novel imprinted sol–gel electrochemical sensor for the determination of propyl gallate (PG) was developed based on a composite of graphene and single walled carbon nanotubes (GR-SWCNTs). It was fabricated by stepwise modifying GR-SWCNTs and molecularly imprinted polymers and stored in 0.10 mol L −1 phosphate buffer solution pH 6.0, which endowed the sensor good sensitivity and selective recognition towards template molecules. The morphology and specific adsorption capacity of the sensor was characterized by scanning electron microscope and electrochemical methods, respectively. Under the optimized conditions, a linear range of the sensor to PG was 8.0 × 10 −8 –2.6 × 10 −3 mol L −1 with a limit of detection of 5.0 × 10 −8 mol L −1 (S/N = 3). The sensor exhibited specificity and selectivity towards template molecules as well as excellent reproducibility, regeneration and stability. Furthermore, the sensor could be applied to determine PG in edible oils, instant noodles and cookies with satisfactory results. [ABSTRACT FROM AUTHOR]

We have combined the molecular imprinting and the layer-by-layer assembly techniques to obtain molecularly imprint polymers (MIPs) for the electrochemical determination of p-nitrophenol ( p-NPh). Silica microspheres functionalized with thiol groups and gold nanoparticles (Au-NPs) were assembled on a gold electrode surface layer by layer. The electrode was then immersed into a solution of pyrrole and p-NPh (the template), and electropolymerization led to the creation of a polymer-modified surface. After the removal of the silica spheres and the template, electrochemical impedance spectroscopy and differential pulse voltammetry (DPV) were employed to characterize the surface. The results demonstrated the successful fabrication of macroporous MIPs embedded with Au-NPs on the gold electrode. The effects of monomer concentration and scan rate on the performance of the electrode were optimized. Excellent recognition capacity is found for p-NPh over chemically similar species. The DPV peak current is linearly related to concentration of p-NPh in the 0.1 μM to 1.4 mM range, with a 0.1 μM limit of detection (at S/N = 3). [Figure not available: see fulltext.] [ABSTRACT FROM AUTHOR]

Molecular imprinting and sol-gel technique were combined to develop a molecular imprinted polymer (MIP) based electrochemical sensor in this work. With the successive modification of multi-walled carbon nanotubes (MWNTs) and gold nanoparticles (GNPs), a modified glassy carbon electrode (GCE) was immersed in a sol-gel solution in the presence of paracetamol (PR) for the electropolymerization to fabricate an imprinted sensor. Scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS), and differential pulse voltammetry (DPV) were employed to characterize the constructed sensor. The factors for the sensor preparation, the electropolymerization potential range, the monomer concentration, and the scan rate for the sensor preparation were optimized. The sensor displayed an excellent recognition capacity toward PR compared with other analogues. Additionally, the DPV peak current was linear to the PR concentration in the range from 8.0 × 10−8to 5.0 × 10−5 mol/L, with a detection limit of 4.0 × 10−8 mol/L. The prepared sensor also showed satisfactory reproducibility and regeneration capacity. [ABSTRACT FROM AUTHOR]

Abstract: A simple and efficient molecularly imprinted polymers (MIPs) based electrochemical sensor were proposed and prepared by electropolymerization of pyrrole in the presence of bovine hemoglobin (BHb) in an aqueous solution. The fabrication process of the sensor was characterized by differential pulse voltammetry and electrochemical impedance spectroscopy, in which [Fe(CN)6]3−/[Fe(CN)6]4− was used as an electrochemical active probe. The influence factors including electropolymerization cycles, scan rate, the concentration of pyrrole, and the extraction conditions were investigated in detailed. Under the optimized conditions, the experimental results showed that the MIPs based sensor possessed a fast rebinding dynamics and an excellent recognition capacity to BHb, compared to the other non-template proteins. Moreover, the prepared sensor also exhibited a dependent relationship between the concentration of template protein and peak current of [Fe(CN)6]3−/[Fe(CN)6]4−. [Copyright &y& Elsevier]