2018
DOI: 10.1016/j.aca.2018.06.045
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Simultaneous electrochemical sensing of warfarin and maycophenolic acid in biological samples

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Cited by 10 publications
(3 citation statements)
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“…These analysis results of CV behaviors show that the dominant peak at m / z = 338.16 is produced by the catalysis of the phenolic hydroxyl group of the MPA molecule. The catalytic oxidation of the phenolic hydroxyl group in MPA involves a two-electron oxidation process, followed by a nucleophilic attack of water molecules at the para position of the hydroxyl group. Accordingly, it can be concluded that an equal number of electrons and protons are involved in the electro-oxidation of MPA molecules on the surface of the 2D Cu–TCPP-modified electrode. According to these results, the catalytic oxidation mechanism of MPA is suggested in Scheme .…”
Section: Resultsmentioning
confidence: 99%
“…These analysis results of CV behaviors show that the dominant peak at m / z = 338.16 is produced by the catalysis of the phenolic hydroxyl group of the MPA molecule. The catalytic oxidation of the phenolic hydroxyl group in MPA involves a two-electron oxidation process, followed by a nucleophilic attack of water molecules at the para position of the hydroxyl group. Accordingly, it can be concluded that an equal number of electrons and protons are involved in the electro-oxidation of MPA molecules on the surface of the 2D Cu–TCPP-modified electrode. According to these results, the catalytic oxidation mechanism of MPA is suggested in Scheme .…”
Section: Resultsmentioning
confidence: 99%
“…It should be noted that the stripping analyses have the lowest limits of detection of any of the commonly used electroanalytical techniques. Gholivand et al 70 developed a ASV method for simultaneous determination of warfarin and mycophenolic acid by using CPE modified with b-cyclodextrin/multi-walled carbon nanotubes/cobalt oxide nanoparticles (b-CD/MWCNTs/Co 3 O 4 NPs/CPE) as working electrode. LOD of reported method for warfarin and mycophenolic acid in serum and urine samples were 0.02 and 0.03 µmol L -1 , respectively.…”
Section: Resonance Light Scattering Methodsmentioning
confidence: 99%
“…TDM requires determining drug concentrations in a biological matrix at certain times relative to administration. Various methods have been proposed for warfarin determination, such as High performance Liquid Chromatography coupled with ultraviolet (UV) [5][6][7] and fluorescence [8] detectors, fluorimetry [9], ultra-performance liquid chromatography tandem mass spectrometry [10], supercritical fluid chromatography-tandem mass spectrometry [11], capillary electrophoresis-mass spectrometry [12] and electrochemistry [13,14].…”
Section: Introductionmentioning
confidence: 99%