Abstract
A new voltammetric sensor is proposed for the simultaneous determination of paracetamol (PAR) and levofloxacin (LEV), using a glassy carbon electrode (GCE) modified with silver nanoparticles (AgNPs), carbon black (CB), and poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS). The modification of the electrode surface was performed by drop-casting dispersion. Morphological characterization of the AgNPs-CB-PEDOT:PSS film was performed by scanning electron microscopy and transmission electron microscopy. The electrochemical behaviors of PAR and LEV were evaluated by cyclic voltammetry in a potential range from 0 to 1.2V, at a scan rate of 0.05Vs−1. Two oxidation peaks were observed during the anodic potential scanning, at potentials of 0.45 (PAR) and 1.0V (LEV). Compared to the bare GCE, the anodic peak currents (ipa) obtained using the AgNPs-CB-PEDOT:PSS/GCE sensor were higher by factors of 5.7 (PAR) and 12 (LEV). The electrochemical determination by square wave voltammetry provided linear concentration ranges of 6.2×10−7 to 7.1×10−6molL−1 (PAR) and 6.7×10−7 to 1.2×10−5mol L−1 (LEV), with detection limits of 1.2×10−8 and 1.4×10−8molL−1 for PAR and LEV, respectively. The AgNPs-CB-PEDOT:PSS/GCE sensor showed good stability, reproducibility, and repeatability, and no interference in the electrochemical determination of PAR and LEV in the presence of other compounds. The proposed method was successfully applied using synthetic urine and river water samples, with recoveries close to 100%.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.