4.8 Article

Electrochemical sensor based on gold nanoparticles fabricated molecularly imprinted polymer film at chitosan-platinum nanoparticles/graphene-gold nanoparticles double nanocomposites modified electrode for detection of erythromycin

Journal

BIOSENSORS & BIOELECTRONICS
Volume 38, Issue 1, Pages 163-169

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2012.05.017

Keywords

Electrochemical sensor; Molecularly imprinted polymers; Graphene-gold nanoparticles composites; Chitosan-platinum nanoparticles composites; Erythromycin detection

Funding

  1. National Natural Science Foundation of the People's Republic of China [30972056, 31171700, 31101296]
  2. National High Technology Research and Development Program of China (National 863 Program of China) [2012AA101604]
  3. Foundation for Outstanding Young Scientist in Shandong Province [BS2009NY001]
  4. Scientific and Technological Development Plan in Shandong Province [2010GNC10960]
  5. Natural Science Foundation of Shandong Province [ZR2010DQ025]
  6. Shandong Province Higher Educational Science and Technology Program [J10LB14]

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A molecularly imprinted electrochemical sensor was fabricated based on gold electrode decorated by chitosan-platinum nanoparticles (CS-PtNPs) and graphene-gold nanoparticles (GR-AuNPs) nanocomposites for convenient and sensitive determination of erythromycin. The synergistic effects of CS-PtNPs and GR-AuNPs nanocomposites improved the electrochemical response and the sensitivity of the sensor. The molecularly imprinted polymers (MIPs) were prepared by HAuCl4, 2-mercaptonicotinic acid (MNA) and erythromycin. Erythromycin and MNA were used as template molecule and functional monomer, respectively. They were first assembled on the surface of GR-AuNPs/CS-PtNPs/gold electrode by the formation of Au-S bonds and hydrogen-bonding interactions. Then the MIPs were formed by electropolymerization of HAuCl4, MNA and erythromycin. The sensor was characterized by cyclic voltammetry (CV), scanning electron microscope (SEM), UV-visible (UV-vis) absorption speactra and amperometry. The linear range of the sensor was from 7.0 x 10(-8) mol/L-9.0 x 10(-5) mol/L, with the limit of detection (LOD) of 2.3 x 10(-8) mol/L (S/N=3). The sensor showed high selectivity, excellent stability and good reproducibility for the determination of erythromycin, and it was successfully applied to the detection of erythromycin in real spiked samples. (C) 2012 Elsevier B.V. All rights reserved.

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