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Carbon Paste Gold Nanoparticles Sensor for the Selective Determination of Dopamine in Buffered Solutions

Source: J. Electrochem. Soc. 157, F116 (2010); doi:10.1149/1.3456629

Published 16 July 2010

KEYWORDS and PACS
Keywords
PACS
  • 82.47.Rs
    Electrochemical sensors
  • 82.45.Fk
    Electrochemical electrodes
  • 87.85.Rs
    Nanotechnologies - applications in biomedical engineering
  • 87.18.Sn
    Neural networks and synaptic communication (biological complexity)
  • YEAR: 2010
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ADDITIONAL INFORMATION
ISSN:
1553-9628 (online)
Publisher:
AIP is a member of CrossRef ECS
Nada F. Atta, Ahmed Galal, Fekria M. Abu-Attia, and Shereen M. Azab
Department of Chemistry, Faculty of Science, University of Cairo, Giza 12613, Egypt
An effective electrochemical sensor for the selective determination of dopamine (DA) in the presence of ascorbic acid (AA) and uric acid (UA) in 0.04  mol  L−1 universal buffer solution (pH 7.4) is introduced. The sensor is based on a carbon paste (CP) electrode modified with gold nanoparticles. In a mixture of DA, AA, and UA, the sensor shows high selective response toward DA and no response for AA or UA. The effect of various experimental parameters including time of deposition of gold nanoparticles on the CP electrode, pH, and scan rate on the voltammetric response of DA was investigated. At the optimum conditions, the concentration of DA was determined using differential pulse voltammetry in a linear range of 1.0×10−7 to 5.0×10−6  mol  L−1 and 5.0×10−6 to 1.3×10−4  mol  L−1 with correlation coefficients of 0.9995 and 0.9988 and a detection limit of 5.9×10−9 and 8.2×10−8  mol  L−1, respectively. The modified electrode can be used for the determination of DA spiked into human serum samples, and excellent recovery results were obtained over a wide concentration range of DA. Moreover, validation parameters, such as reproducibility, sensitivity, and recovery were evaluated successfully in the determination of DA in diluted human urine. ©2010 The Electrochemical Society
History: Submitted 12 February 2010; revised 26 April 2010; published 16 July 2010
Permalink: http://dx.doi.org/10.1149/1.3456629

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