Abstract

In this research, the manufacturing of highly sensitive and effective electrochemical sensor is presented. It is based on silver nanoparticles/poly(3-methylthiophene) (Ag–NPs/P3MT) nanocomposite for the detection of galantamine hydrobromide (Gal). In this process, Ag–NPs/P3MT modified electrode was fabricated by electro-polymerization of 3-methylthiophene (3MT) in the presence of silver nitrate on the surface of the glassy carbon electrode (GCE). Scanning electron microscopy (SEM), field emission scanning electron microscopy (FE–SEM) and energy dispersive X–ray (EDX) analysis were employed to characterize the constructed sensor. Compared with unmodified and P3MT modified electrodes, the Ag–NPs/P3MT modified electrode demonstrated superb electrochemical catalytic activity and significantly enhanced the oxidation peak current of Gal. The experimental parameters, such as supporting electrolyte and its pH, the number of cycles for the electro-polymerization and the scan rate for the sensor preparation were optimized. Under the optimal conditions, the proposed electrode exhibited excellent sensing performance for detecting of Gal using differential pulse voltammetry over the concentration range of 1.0 to 700μM and a detection limit of 0.18μM. Finally, the excellent results showed that the modified electrode can be successfully applied to quantitatively measure of Gal in human cerebrospinal fluid (CSF), Narcissus and pharmaceutical real samples with satisfactory consequences.

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.