Dinuclear copper(II) octaazamacrocyclic complex in a PVC coated GCE and graphite as a voltammetric sensor for determination of gallic acid and antioxidant capacity of wine samples
Abstract:A novel efficient differential pulse voltammetric (DPV) method for determination gallic acid (GA) was developed by using an electrochemical sensor based on [Cu2tpmc](ClO4)4 immobilized in PVC matrix and coated on graphite (CGE) or classy carbon rod (CGCE). The proposed method is based on the gallic acid oxidation process at formed [Cu2tpmcGA](3+) complex at the electrode surface. The complexation was explored by molecular modeling and DFT calculations. Voltammograms for both sensors, recorded in a HNO3 as a su… Show more
“…This can be attributed to the sharp and high potential peak value for the COLC oxidation at BDDE, using the developed procedure. Similar to these compounds, some phenolic compounds (gallic acid, caffeine, chlorogenic acid, vanillin) also do not interfere with COLC determination as at higher pH (such as in this study 7.5) they do not show electrochemical response or they provide broad peak at lower potentials . These compounds usually provide oxidation behavior at potentials lower than 1 V, and this potential with increase of pH is followed with potential shift to more negative potentials.Obviously, DNA also does not interfere with COLC, indicating possible determination of this compound in biological samples (Figure B).…”
Colchicine (COLC) is a natural toxic product and secondary metabolite most commonly used to treat gout. In this study, its electrochemical behavior and determination was investigated by employing modification‐free boron‐doped diamond electrode (BDDE). Besides, its interaction with DNA was monitored using electrochemical methods. It was found that oxidation of this compound proceeds in two steps, where first sharp and well defined oxidation peak occurs at potential of around 1.19 V, and second one at around 1.37 V, in Britton‐Robinson buffer solution at pH 7.5. Wide dynamic range from 1 to 100 μM was obtained with a detection limit (3σintercept/slope) of a 0.26 μM, based on the evaluation of first oxidation peak using differential pulse voltammetry. The proposed method was also found to be suitable for monitoring interaction of this drug with DNA as important segment for medical use. Concerning the validation, the analytical procedure shows excellent selectivity and sensitivity toward COLC detection and after method development it was successfully used for its quantification in pharmaceutical preparation and human serum sample, with satisfactory recovery. Obviously, this approach can be promising replacement for time‐consuming and expensive separation methods.
“…This can be attributed to the sharp and high potential peak value for the COLC oxidation at BDDE, using the developed procedure. Similar to these compounds, some phenolic compounds (gallic acid, caffeine, chlorogenic acid, vanillin) also do not interfere with COLC determination as at higher pH (such as in this study 7.5) they do not show electrochemical response or they provide broad peak at lower potentials . These compounds usually provide oxidation behavior at potentials lower than 1 V, and this potential with increase of pH is followed with potential shift to more negative potentials.Obviously, DNA also does not interfere with COLC, indicating possible determination of this compound in biological samples (Figure B).…”
Colchicine (COLC) is a natural toxic product and secondary metabolite most commonly used to treat gout. In this study, its electrochemical behavior and determination was investigated by employing modification‐free boron‐doped diamond electrode (BDDE). Besides, its interaction with DNA was monitored using electrochemical methods. It was found that oxidation of this compound proceeds in two steps, where first sharp and well defined oxidation peak occurs at potential of around 1.19 V, and second one at around 1.37 V, in Britton‐Robinson buffer solution at pH 7.5. Wide dynamic range from 1 to 100 μM was obtained with a detection limit (3σintercept/slope) of a 0.26 μM, based on the evaluation of first oxidation peak using differential pulse voltammetry. The proposed method was also found to be suitable for monitoring interaction of this drug with DNA as important segment for medical use. Concerning the validation, the analytical procedure shows excellent selectivity and sensitivity toward COLC detection and after method development it was successfully used for its quantification in pharmaceutical preparation and human serum sample, with satisfactory recovery. Obviously, this approach can be promising replacement for time‐consuming and expensive separation methods.
“…The estimated TPC value is found to be 277.4 mg L −1 . The observed higher value can be attributed to the fact that all phenols in the real samples can be detected by this method, and furthermore, the Folin–Ciocalteu reagent may react with many nonphenolic substances [ 31 ]. This problem can be resolved by using the sensor since the nonphenolic compounds have no interference with the response of the polyphenols.…”
SummaryA simple and sensitive poly(gallic acid)/multiwalled carbon nanotube modified glassy carbon electrode (PGA/MWCNT/GCE) electrochemical sensor was prepared for direct determination of the total phenolic content (TPC) as gallic acid equivalent. The GCE working electrode was electrochemically modified and characterized using scanning electron microscope (SEM), cyclic voltammetry (CV), chronoamperometry and chronocoulometry. It was found that gallic acid (GA) exhibits a superior electrochemical response on the PGA/MWCNT/GCE sensor in comparison with bare GCE. The results reveal that a PGA/MWCNT/GCE sensor can remarkably enhance the electro-oxidation signal of GA as well as shift the peak potentials towards less positive potential values. The dependence of peak current on accumulation potential, accumulation time and pH were investigated by square-wave voltammetry (SWV) to optimize the experimental conditions for the determination of GA. Using the optimized conditions, the sensor responded linearly to a GA concentration throughout the range of 4.97 × 10−6 to 3.38 × 10−5 M with a detection limit of 3.22 × 10−6 M (S/N = 3). The fabricated sensor shows good selectivity, stability, repeatability and (101%) recovery. The sensor was successfully utilized for the determination of total phenolic content in fresh pomegranate juice without interference of ascorbic acid, fructose, potassium nitrate and barbituric acid. The obtained data were compared with the standard Folin–Ciocalteu spectrophotometric results.
“…Up to now, there are several electroanalytical methods reported for the determination of the total antioxidant capacity (Pekec et al 2013;Rebelo et al 2013;Tirawattanakoson et al 2016;Gao et al 2015;Petkovic et al 2015) and chromatographic methods using different detectors such as highperformance liquid chromatography (HPLC) in combination with electrospray ionization tandem mass spectrometry (Lijia et al 2014), with nuclear magnetic resonance and mass spectroscopy (NMR-MS) (Lommen et al 2000;Tsao et al 2003), Electronic supplementary material The online version of this article (doi:10.1007/s12161-017-0935-x) contains supplementary material, which is available to authorized users.…”
A boron-doped diamond electrode was used as an electrochemical sensor for the determination of phlorizin (aka phloridzin, phlorrhizin) using square wave voltammetry (SWV). Phlorizin (Phl) exhibited a well-defined oxidation peak at +0.9 V (versus Ag/AgCl electrode 3 M KCl) in solutions with a pH value of 6.0. Parameters such as pH value and scan rate were optimized for cyclic voltammetry as well as amplitude and frequency for SWV. The sensor gave excellent response with a wide linear dynamic range for concentrations of phlorizin from 3 to 100 μM with a detection limit of 0.23 μM and a good repeatability (± 0.9%, n = 7 measurements, c = 10 μM). The effect of interferences by most common compounds was tested, and the method was successfully applied to the determination of the title compound in apple root extracts and urine samples with satisfactory recovery.
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