4.7 Article

Electrochemical droplet-based microfluidics using chip-based carbon paste electrodes for high-throughput analysis in pharmaceutical applications

Journal

ANALYTICA CHIMICA ACTA
Volume 883, Issue -, Pages 45-54

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.aca.2015.03.008

Keywords

Droplet-based microfluidics; Carbon paste electrode; Dopamine; Ascorbic acid; Chronoamperometry; Electrochemical detection

Funding

  1. National Research University Project
  2. Office of Higher Education Commission [WCU-032-AM-57]
  3. Thailand Research Fund [RTA5780005]
  4. Ratchadaphiseksomphot Endowment Fund

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This paper presents the first example of a pharmaceutical application of droplet-based microfluidics coupled with chronoamperometric detection using chip-based carbon paste electrodes (CPEs) for determination of dopamine (DA) and ascorbic acid (AA). Droplets were generated using an oil flow rate of 1.80 mu L min(-1), whereas a flow rate of 0.80 mu L min(-1) was applied to the aqueous phase, which resulted in a water fraction of 0.31. The optimum applied potential for chronoamperometric measurements in droplets was found to be 150 mV. Highly reproducible analysis of DA and AA was achieved with relative standard deviations of less than 5% for both intra-day and inter-day measurements. The limit of detection (LOD) and limit of quantitation (LOQ) were found to be 20 and 70 mu M for DA and 41 and 137 mu M for AA, respectively. Linearity of this method was in the ranges of 0.02-3.0 mM for DA and 0.04-3.0 mM for AA. This system was successfully applied to determine the amounts of DA and AA in intravenous drugs. Calibration curves of DA and AA for quantitative analysis were obtained with good linearity with R-2 values of 0.9984 and 0.9988, respectively. Compared with the labeled amounts, the measured concentrations of DA and AA obtained from this system were insignificantly different, with error percentages of less than +/- 3.0%, indicating a high accuracy of the developed method. (C) 2015 Elsevier B.V. All rights reserved.

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