Abstract

A new nanocomposite imprinted electrochemical sensor was developed for sensitive and selective determination of acetylsalicylic acid (ASA), based on a gold electrode modified with one-step electropolymerization of the molecularly imprinted polymer (MIP) composed from polypyrrole (ppy), sol-gel, Silica@Gold core-Shell nanoparticles (SiO2@AuNPs) and acetylsalicylic acid. SiO2@AuNPs were introduced into the polymer matrix for the enhancement of electrical response of [Fe(CN)6]3−/[Fe(CN)6]4− redox pair which was used as an electrochemical active probe. The SiO2@AuNPs, were synthesized chemically by using a modified Stober method and they were characterized by UV–Vis spectrophotometry, Fourier transform infrared (FT-IR) spectrometry, X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Under the optimized experimental conditions, two linear concentration ranges from 1.0 to 10.0nM and 10.0–100.0nM with a limit of detection (LOD) of 0.2nM was obtained. The effects of interfering species on the determination of ASA were investigated and it was found that the proposed sensor has a high recognition capacity towards the ASA in the presence of interfering species in solutions. Moreover, the reproducibility, repeatability and stability of the imprinted sensor were all found to be satisfactory. Finally, the modified electrode was successfully applied for determination of ASA in tablet and urine samples.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.