Analytical and Bioanalytical Chemistry

, Volume 386, Issue 7–8, pp 2087–2094 | Cite as

Selective detection of dopamine in the presence of ascorbic acid by use of glassy-carbon electrodes modified with both polyaniline film and multi-walled carbon nanotubes with incorporated β-cyclodextrin

Original Paper

Abstract

A simple, sensitive, and reliable method based on a combination of multi-walled carbon nanotubes with incorporated β-cyclodextrin (β-CD-MWNTs) and a polyaniline (PANI) film-modified glassy-carbon (GC) electrode has been successfully developed for determination of dopamine (DA) in the presence of ascorbic acid (AA). The PANI film had good anti-interference properties and long-term stability, because of the permselective and protective properties of the conducting redox polymer film. The acid-treated MWNTs with carboxylic acid functional groups promoted the electron-transfer reaction of DA and inhibited the voltammetric response of AA. Sensitive detection of DA was further improved by the preconcentration effect of formation of a supramolecular complex between β-CD and DA. The analytical response of the β-CD-MWNTs/PANI film to the electrochemical behavior of DA was, therefore, better than that of a MWNTs/PANI film, a PANI film, or a bare glassy-carbon (GC) electrode. Under the conditions chosen a linear calibration plot was obtained in the range 1.0 × 10−7–1.0 × 10−3 mol L−1 and the detection limit was 1.2 × 10−8 mol L−1. Interference from AA was effectively eliminated and the sensitivity, selectivity, stability, and reproducibility of the electrodes was excellent for determination of DA.

Keywords

Dopamine β-Cyclodextrin Multi-walled carbon nanotubes Polyaniline 

Notes

Acknowledgements

This work was supported by Specialized Research Fund for the Doctoral Program of Higher Education (SRFDP).

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Copyright information

© Springer-Verlag 2006

Authors and Affiliations

  1. 1.State Key Laboratory of Chemical, Biological Sensing Technologies and ChemometricsHunan UniversityChangshaPeople’s Republic of China

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