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Graphene-polyaniline modified electrochemical droplet-based microfluidic sensor for high-throughput determination of 4-aminophenol
Authors:Poomrat Rattanarat  Akkapol Suea-Ngam  Nipapan Ruecha  Weena Siangproh  Charles S. Henry  Monpichar Srisa-Art  Orawon Chailapakul
Affiliation:1. Electrochemistry and Optical Spectroscopy Research Unit (EOSRU), Department of Chemistry, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand;2. Chromatography and Separation Research Unit (ChSRU), Department of Chemistry, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand;3. Program in Macromolecular Science, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand;4. Department of Chemistry, Faculty of Science, Srinakharinwirot University, Sukhumvit 23, Wattana, Bangkok 10110, Thailand;5. Department of Chemistry, Colorado State University, Fort Collins, CO 80523, United States;6. School of Biomedical Engineering, Colorado State University, Fort Collins, CO 80523, United States;g National Center of Excellent of Petroleum, Petrochemicals and Advanced Materials, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand
Abstract:We report herein the first development of graphene-polyaniline modified carbon paste electrode (G-PANI/CPE) coupled with droplet-based microfluidic sensor for high-throughput detection of 4-aminophenol (4-AP) in pharmaceutical paracetamol (PA) formulations. A simple T-junction microfluidic platform using an oil flow rate of 1.8 μL/min and an aqueous flow rate of 0.8 μL/min was used to produce aqueous testing microdroplets continuously. The microchannel was designed to extend the aqueous droplet to cover all 3 electrodes, allowing for electrochemical measurements in a single droplet. Parameters including flow rate, water fraction, and applied detection potential (Edet) were investigated to obtain optimal conditions. Using G-PANI/CPE significantly increased the current response for both cyclic voltammetric detections of ferri/ferrocyanide [Fe(CN)6]3−/4− (10 times) and 4-AP (2 times), compared to an unmodified electrode. Using the optimized conditions in the droplet system, 4-AP in the presence of PA was selectively determined. The linear range of 4-AP was 50–500 μM (R2 = 0.99), limit of detection (LOD, S/N = 3) was 15.68 μM, and limit of quantification (LOQ, S/N = 10) was 52.28 μM. Finally, the system was used to determine 4-AP spiked in commercial PA liquid samples and the amounts of 4-AP were found in good agreement with those obtained from the conventional capillary zone electrophoresis/UV–Visible spectrophotometry (CZE/UV–Vis). The proposed microfluidic device could be employed for a high-throughput screening (at least 60 samples h−1) of pharmaceutical purity requiring low sample and reagent consumption.
Keywords:Droplet-based microfluidics   Electrochemical detection   Graphene   Polyaniline   4-Aminophenol   Paracetamol
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