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Determination of Diclofenac Using Electromembrane Extraction Coupled With Stripping Fft Continuous Cyclic Voltammetry Publisher Pubmed



Mofidi Z1 ; Norouzi P1, 2 ; Seidi S3 ; Ganjali MR1, 2
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Authors Affiliations
  1. 1. Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran, Tehran, Iran
  2. 2. Biosensor Research Center, Endocrinology & Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Analytical Chemistry, Faculty of Chemistry, K.N. Toosi University of Technology, Tehran, Iran

Source: Analytica Chimica Acta Published:2017


Abstract

For the first time, on-line and ultra-sensitive determination of trace amount of diclofenac in whole blood sample was performed by coupling of electromembrane extraction (EME) and stripping fast Fourier transform continuous cyclic voltammetry (SFFTCCV). In SFFTCCV, the potential waveform was continuously applied on a carbon paste electrode and the electrode response was obtained by subtracting the background current and integrating the current in potential range of the analyte oxidation. A central composite design was used for the optimization of the parameters influencing the extraction efficiency. By applying a DC potential of 20 V during 28 min of extraction, diclofenac was migrated from the sample solution (pH 5), into a thin layer of 1-octanol immobilized in the pores of a porous flat sheet membrane and then into the acceptor solution (pH 7). The method presented a good linearity within the range of 5–1000 ng mL−1 with a determination coefficient of 0.993 in whole blood samples. Limits of detection (LOD) and quantification (LOQ) were found to be 1.0 ng mL−1 and 5.0 ng mL−1 respectively. © 2017 Elsevier B.V.
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