2011
DOI: 10.2116/analsci.27.991
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Electroanalysis and Simultaneous Determination of 6-Thioguanine in the Presence of Uric Acid and Folic Acid Using a Modified Carbon Nanotube Paste Electrode

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Cited by 83 publications
(25 citation statements)
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“…The anodic peak potential of MTX is shifted negatively with the increase of the pH value, indicating reactions accompanied by proton transfer. The slopes of 63.6 mV/pH for MTX oxidation is nearby to the theoretical value of 59 mV/pH and pointed out toward two protons and two electrons involved in the oxidation process [28][29][30]. The detection limit (LOD) was estimated by applying the standard formula of LOD = 3sb/m [31], where m is the slope of the calibration curve and sb is the standard deviation of the peak currents of the blank solution (five replicates).…”
Section: Relationship Between Ph Peak Potential and Peak Current Valuessupporting
confidence: 67%
“…The anodic peak potential of MTX is shifted negatively with the increase of the pH value, indicating reactions accompanied by proton transfer. The slopes of 63.6 mV/pH for MTX oxidation is nearby to the theoretical value of 59 mV/pH and pointed out toward two protons and two electrons involved in the oxidation process [28][29][30]. The detection limit (LOD) was estimated by applying the standard formula of LOD = 3sb/m [31], where m is the slope of the calibration curve and sb is the standard deviation of the peak currents of the blank solution (five replicates).…”
Section: Relationship Between Ph Peak Potential and Peak Current Valuessupporting
confidence: 67%
“…Thus, some references may be mentioned: for instance, the determination of captopril, thioguanine and levodopa (Beitollahi et al, 2014(Beitollahi et al, , 2011a(Beitollahi et al, , 2011b, L-cysteine with ascorbic acid, (Raoof et al, 2007(Raoof et al, , 2006a(Raoof et al, , 2006b, hydroquinone derivatives (Taleat et al, 2008) and simultaneous determinations of carbidapa (Tajik et al, 2013).…”
Section: Introductionmentioning
confidence: 99%
“…One of the most important properties of CMEs is their ability to catalyze the electrode process via the significant decrease of overpotential with respect to the unmodified electrode. With respect to the relatively selective interaction of the electron mediator with the target analyte in a coordinated fashion, these electrodes are capable of considerably enhancing the selectivity of electroanalytical methods (Beitollahi et al 2011a;Luo et al 2013;Taleat et al 2008;Huo et al 2013;Thomas et al 2013b;Raoof et al 2006b;Oliveira et al 2013;Beitollahi et al 2011b;Thomas et al 2013c;Mohammadi et al 2013;Sanghavi et al 2013;Beitollahi et al 2014;Li et al 2012;Ghoreishi et al 2012;Yildiz et al 2014).…”
Section: Introductionmentioning
confidence: 99%