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Title: | Ultra-performance liquid chromatography coupled with graphene/polyaniline nanocomposite modified electrode for the determination of sulfonamide residues |
Authors: | Thammasoontaree N. Rattanarat P. Ruecha N. Siangproh W. Rodthongkum N. Chailapakul O. |
Keywords: | Amides Chemical detection Graphene Liquid chromatography Nanocomposites Phase separation Polyaniline Potassium compounds Shellfish Sulfur compounds Boron-doped diamond electrodes ELectrochemical detection Electrospraying Hydrodynamic voltammetry Screen-printed carbon electrodes Sulfonamides Ultra performance liquid chromatography UPLC Electrodes acetonitrile acetonitrile derivative alcohol aniline derivative graphite nanocomposite phosphate polyaniline potassium derivative potassium dihydrogen phosphate sulfonamide animal chemical structure chemistry devices electrochemical analysis electrode high performance liquid chromatography isolation and purification Penaeidae procedures reproducibility scanning electron microscopy solid phase extraction transmission electron microscopy ultrastructure Acetonitriles Aniline Compounds Animals Chromatography, High Pressure Liquid Electrochemical Techniques Electrodes Ethanol Graphite Microscopy, Electron, Scanning Microscopy, Electron, Transmission Molecular Structure Nanocomposites Penaeidae Phosphates Potassium Compounds Reproducibility of Results Solid Phase Extraction Sulfonamides |
Issue Date: | 2014 |
Abstract: | An ultra-performance liquid chromatography (UPLC) coupled with graphene/polyaniline (G/PANI)-modified screen-printed carbon electrode was developed for separation and sensitive determination of eight sulfonamides (SAs) in shrimp. Electrospraying was selected for electrode modification because it can generate the well dispersion of G/PANI nanocomposites on the electrode surface. Prior to electrochemical detection, eight SAs were completely separated within 7 min by using reversed phase UPLC (C4) with mobile phase containing 70:25:5 (v/v/v) of potassium hydrogen phosphate (pH 3):acetonitrile:ethanol. For amperometric detection, the detection potential acquired from hydrodynamic voltammetry was found to be +1.4 V. Under optimal conditions, a wide linearity and low limit of detection were obtained for eight SAs in the range of 0.01-10 μg mL-1 and 1.162-6.127 ng mL-1, respectively. Compared to boron-doped diamond (BDD) electrode, a G/PANI-modified screen-printed carbon electrode offered higher sensitivity with lower operating cost. To determine SAs in shrimp samples, solid-phase extraction was used to clean up and preconcentrate the samples prior to UPLC separation. To validate this developed method, a highly quantitative agreement was accomplished with UPLC-UV system. Thus, this proposed system might be an alternative approach for rapid, inexpensive, and sensitive determination of SAs in shrimps. © 2014 Elsevier B.V. All rights reserved. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/13930 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84894542854&doi=10.1016%2fj.talanta.2014.02.004&partnerID=40&md5=a0e821fe823d9adbf13db8151f80365c |
ISSN: | 399140 |
Appears in Collections: | Scopus 1983-2021 |
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