ZnO nanoparticle-modified ionic liquid-carbon paste electrodefor voltammetric determination of folic acid in food and pharmaceutical samples

In this work, a ZnO/nanoparticles (NPs) modified carbon ionic liquid paste electrode (ZnO/NP/CILPE) was fabricated and used to investigate the electrochemical behavior of folic acid. ZnO/NP/CILPE was prepared by mixing hydrophilic ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate ([C₄mim]-[PF₆])), ZnO/NPs, graphite powder, and liquid paraffin together. The fabricated ZnO/NP/CILPE showed great electrocatalytic ability to the oxidation of folic acid, and an irreversible oxidation peak appeared at 0.75 V (vs. Ag/AgCl) with improved peak current. Under the optimized conditions of pH 9.0, the plot of peak current vs. folic acid concentration consisted of two linear segments with slopes of 1.776and 0.033 μA/μM in the concentration ranges of 0.05–1.5 μM and 1.5–550.0 μM, respectively. The detection limit was 0.01 μM (3σ). The proposed sensor was successfully applied for the determination of folic acid in fortified food and pharmaceutical samples.     

Enhanced electrocatalytic oxidation of hydroxylamine on Pt/polypyrrole composite modified glassy carbon electrode

A sensitive hydroxylamine sensor is developed by electrodeposition of Pt nanoparticles on pre-synthesized polypyrrole nanoparticles modified glassy carbon electrode. The modified electrode presents distinctly electrocatalytic activity toward hydroxylamine oxidation. The kinetic parameters such as the overall numbers of electrons involved in hydroxylamine oxidation, the electron transfer coefficient, standard heterogeneous rate constant, and diffusion coefficient are evaluated. The current response increases linearly with increasing hydroxylamine concentrations and exhibits two wide linear ranges of 5.0?×?10^?7–1.1?×?10^?3 and 1.1?×?10^?3–18.8?×?10^?3 M with a detection limit of 0.08 μM (s/n?=?3). The proposed electrode presents excellent operational and storage ability for determining hydroxylamine. Moreover, the sensor shows good sensitivity, selectivity, and reproducibility properties.     

Electrochemical and catalytic investigations of epinephrine,acetaminophen and folic acid at the surface of titanium dioxide nanoparticle-modified carbon paste electrode

In the present paper, the use of a carbon paste electrode modified with 1-(4-(1, 3-dithiolan-2-yl)-6, 7-dihydroxy-2-methyl-6, 7-dihydrobenzofuran-3-yl)ethanone (DDE) and TiO₂ nanoparticles prepared by a simple and rapid method was described. The modified electrode showed excellent properties for electrocatalytic oxidization of epinephrine (EP), acetaminophen (AC) and folic acid (FA). The apparent charge transfer rate constant, k _s?=?1.14 s^?1, and transfer coefficient, α?=?0.54, for electron transfer between the modifier and carbon paste electrode were calculated. It has been found that under optimum condition (pH?=?7.0) in cyclic voltammetry, the oxidation of EP occurs at a potential about 280 mV less positive than that of an unmodified carbon paste electrode. The values of transfer coefficients (α?=?0.46), catalytic rate constant (k?=?1.2?×?10⁴ M^?1 s^?1) and diffusion coefficient (D?=?2.70?×?10^?5 cm² s^?1) were calculated for EP. Differential pulse voltammetry (DPV) exhibited two linear dynamic ranges of 0.5 to 50.0 μM and 50.0 to 1,000 μM for EP. This modified electrode is quite effective not only for the detection of EP, AC and FA but also for the simultaneous determination of these species in a mixture. The limit of detection for EP, AC and FA is 0.10, 1.80 and 2.36 μM, respectively.     

Electrocatalytic oxidation of <Emphasis Type="SmallCaps">l</Emphasis>-tyrosine at carboxylic acid functionalized multi-walled carbon nanotubes modified carbon paste electrode

The electrocatalytic oxidation of l-tyrosine (Tyr) was investigated on a carboxylic acid functionalised multi-walled carbon nanotubes modified carbon paste electrode using cyclic voltammetry and amperometry. The surface morphology of the electrodes was studied using field emission (FE)-SEM images, and the interface properties of bare and modified electrodes were investigated by electrochemical impedance spectroscopy (EIS). The influence of the amount of modifier loading and the variation of the pH of the solution on the electrochemical parameters have been investigated. Cyclic voltammetry was carried out to study the electrochemical oxidation mechanism of Tyr, which showed an irreversible oxidation process at a potential of 637.0 mV at modified electrode. The anodic peak current linearly increased with the scan rate, suggesting that the oxidation of Tyr at modified electrode is an adsorption-controlled process. A good linear relationship between the oxidation peak current and the Tyr concentration in the range of 0.8–100.0 μM was obtained in a phosphate buffer solution at pH 7.0 with a detection limit of 14.0?±?1.36 nM (S/N?=?3). The practical utility of the sensor was demonstrated by determining Tyr in spiked cow’s milk and human blood serum. The modified electrode showed excellent reproducibility, long-term stability and antifouling effects.     

Benzoylferrocene-modified carbon nanotubes paste electrode as a voltammetric sensor for determination of hydrochlorothiazide in pharmaceutical and biological samples

The electrooxidation of hydrochlorothiazide (HCT) at the surface of a benzoylferrocene modified multi-walled carbon nanotube paste electrode was studied using electrochemical approaches. Under the optimized conditions (pH 7.0), the square wave voltammetric peak current of HCT increased linearly with HCT concentration in the ranges of 6.0?×?10^?7 to 3.0?×?10^?4 M. The detection limit was 9.0?×?10^?8 M HCT. The diffusion coefficient (D?=?1.75?×?10^?5 cm²/s) and electron transfer coefficient (α?=?0.45) for HCT oxidation were also determined. The proposed sensor was successfully applied for the determination of HCT in human urine and tablet samples.     

Nitrogen-doped multi-walled carbon nanotubes for paracetamol sensing

A novel sensor consisting of nitrogen-doped multi-walled carbon nanotubes was fabricated by means of chemical vapor deposition technique with decomposition of acetonitrile onto oxidized silicon wafer using ferrocene as catalyst. The electrochemical response of carbon nanotubes-based sensor towards oxidation of paracetamol to N-acetyl-p-quinone imine was investigated in phosphate buffer solution (pH 7.0) by means of standard electrochemical techniques. A quasi-reversible response for oxidation of paracetamol was identified on carbon nanotubes-based sensor with detection limit and sensitivity of 0.485 μM and 0.8406 A M^?1 cm^?2, respectively. It was found that the nitrogen doping in carbon nanotubes enhances the sensor's detection ability. Namely, electrochemical studies performed on film consisting of pristine carbon nanotubes reveal as well quasi-reversible response towards oxidation of paracetamol but nevertheless poorer detection ability and sensitivity (0.950 μM; 0.601 A M^?1 cm^?2). The findings strongly suggest the application of nitrogen-doped carbon nanotubes in biosensing.     

Sensitive voltammetric determination of cysteamine using promazine hydrochloride as a mediator and modified multi-wall carbon nanotubes carbon paste electrodes

This paper presents a sensitive electrochemical method for the determination of cysteamine (CA) using promazine hydrochloride-modified multi-wall carbon nanotubes carbon paste electrode (PrH/MWCNTs CPE). Because of the good electrochemical activity of MWCNTs and the acceptable performance of promazine hydrochloride (PrH) as an electrocatalytic mediator, the modified electrode significantly enhanced the sensitivity for the detection of CA in comparison to the bare carbon paste electrode (CPE). All chemical parameters such as pH of solution, concentration of PrH and kinetic parameters of the system were investigated. Linear sweep voltammetric (LSV) method was used to follow the electrocatalytic effect of CA on the current–potential response of PrH. Under optimum conditions, the obtained net peak current ?I _p(I _sample???I _blank) was linear with CA concentrations in two dynamic ranges of 2.0–346.5 μmol l^?1 (?I _p?=?(0.0195?±?0.0043)C _CA?+?(0.7648?±?0.0397) (r ²?=?0.9948)) and 346.5–1,912.5 μmol l^?1 (?I _p?=?(0.0100?±?0.0026)C _CA?+?(3.8981?±?0.0828) (r ²?=?0.9911)) with a detection limit of 0.8 μmol l^?1. Finally, the PrH/MWCNTs CPE was successfully applied for the determination of CA in urine and drug samples with satisfactory results.     

Electrochemical methods for determination of thymine in medical pipefish samples based on HPMαFP/Ppy/GCE-modified electrode

A sensitive electrochemical method was developed for the voltammetric determination of thymine at a composite film-modified electrode 1-phenyl-3-methyl-4-(2-furoyl)-5-pyrazolone (HPMαFP)/polypyrrole (Ppy)/glassy carbon electrode (GCE). The electrochemical parameters of thymine were investigated by cyclic voltammetry and differential pulse voltammetry. In pH?=?7.4, one sensitive oxidation peak of thymine with E _pa?=?0.968 V was observed on the HPMαFP/PPy-modified electrode. The difference of peak potential (?E _pa) was 188 mV lower than that for bare GCE. Compared to the bare GCE and Ppy/GCE, the HPMαFP/Ppy/GCE-modified electrode showed an excellent electrocatalytic effect on the oxidation of thymine and displayed a shift of the oxidation potential in the negative direction with significant increase in the peak current. Under the optimum condition, the concentration calibration range and detection limit are 2?×?10^?6–1?×?10^?4 and 4.85?×?10^?7?M for thymine. This developed method had been applied to the direct determination of thymine in medical pipefish samples with satisfactory results.     

Voltammetric sensor for simultaneous determination of ascorbic acid,acetaminophen, and tryptophan in pharmaceutical products

A novel carbon paste electrode modified with carbon nanotubes and 5-amino-2′-ethyl -biphenyl-2-ol was fabricated. The electrochemical study of the modified electrode, as well as its efficiency for electrocatalytic oxidation of ascorbic acid (AA), is described. The electrode was employed to study the electrocatalytic oxidation of AA, using cyclic voltammetry, chronoamperometry, and square-wave voltammetry (SWV) as diagnostic techniques. It has been found that the oxidation of AA at the surface of modified electrode occurs at a potential of about 250 mV less positive than that of an unmodified carbon paste electrode. SWV exhibits a linear dynamic range from 2.0?×?10^?7 to 5.0?×?10^?4 M and a detection limit of 1.0?×?10^?7 M for AA. In addition, this modified electrode was used for simultaneous determination of AA, acetaminophen (AC), and tryptophan (TRP). Finally, the modified electrode was used for determination of AA, AC, and TRP in pharmaceutical products.     

A sensitive amperometric detection of dopamine agonist drug pramipexole at functionalized multi-walled carbon nanotubes (f-MWCNTs) modified electrode

The electrochemical detection of dopaminergic agonist drug pramipexole dihydrochloride monohydrate (PPX) has been investigated by cyclic voltammetric (CV) and amperometric i–t techniques at functionalized multi-walled carbon nanotubes-modified glassy carbon electrode. For the first time, a sensitive and rapid electrochemical method was developed for the determination of PPX. The surface morphological characteristics of the proposed electrode have been studied by using transmission electron microscopy (TEM); further, electrochemical impedance spectroscopy (EIS) and Fourier transform infrared spectroscopy (FTIR) have been employed. PPX shows an irreversible anodic peak, which may be ascribed to the oxidation of the –NH groups of PPX. The proposed method was showing good sensitivity of 0.993 μA μM^?1 cm^?2 with a linear range of 5 to 340 μM by amperometric i–t and CV technique shows a linear range of 12.5 to 313 μM with a sensitivity of 1.92 μA μM^?1 cm^?2. The recovery of PPX from blood serum samples was found 100.6 and 98.9 %, respectively. Furthermore, the proposed method has been demonstrated for the determination of PPX in commercially available pharmaceutical samples and good agreement of results obtained.     

Electrooxidation of hydrazine in alkaline medium at carbon paste electrode decorated with poly(<Emphasis Type="Italic">P</Emphasis>-phenylendiamine/ZnO) nanocomposite

In this study, poly(P-phenylenediamine/ZnO) (PpPD/ZnO) nanocomposite (NC) under ultrasonic conditions was synthesized and characterized. The presence of zinc oxide nanoparticles changed the morphology of PpPD considerably as confirmed by SEM observations. Hydrazine electrooxidation at novel modified carbon paste electrodes (CPE) with supported NC was investigated by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and chronoamperometry (CA) techniques. Obtained results showed that the NC increases the surface catalytic activity of CPE toward hydrazine electrooxidation. The electrocatalytic current density increased linearly with hydrazine concentration, and the detection limit and sensitivity are determined to be 24 μM and 0.172 mA cm^?2 mM^?1, respectively. As revealed by the EIS measurements, the increased conductivity and decreased R _ct are owing to the presence of ZnO NPs in the PpPD matrix. The CA results indicated that hydrazine electrooxidation results in higher steady-state current density on CPE/PpDP/ZnO electrode system compared to the CPE/PpDP and CPE electrodes.     

Nanomolar detection limit for determination of norepinephrine in the presence of acetaminophen and tryptophan using carbon nanotube-based electrochemical sensor

A carbon paste electrode modified by carbon nanotubes and a synthesized hydroquinone derivative (abbreviated as DHB) was fabricated. It was used as an electrochemical sensor for simultaneous determination of norepinephrine (NE), acetaminophen (AC), and tryptophan (Trp). Oxidation potential of NE decreased about 220 mV at the modified electrode in comparison with unmodified electrode because of electrocatalysis of oxidation of NE via E? mechanism at the modified electrode. Differential pulse voltammetry was used for obtaining the calibration plot of NE and two linear range of 0.2–20.0 μM and 20.0–1,500.0 μM and an interesting detection limit (3σ) of 40.0 nM were obtained for NE. Also, simultaneous determination of NE, AC, and Trp was described by the proposed sensor and linear range of 20.0–800.0 μM was found for AC and Trp. Finally, the electrochemical sensor was used for the determination of NE, AC, and Trp in mixture.     

Ultrasonic preparation of tetraoxalyl ethylenediamine melamine resin-coated multiwalled carbon nanotubes for trace Ni(II) sensing

Under an aid of ultrasonic, tetraoxalyl ethylenediamine melamine resin-coated multiwalled carbon nanotubes were prepared for Ni(II) sensing in aqueous solution. The processes involved the fabrication of tetraoxalyl ethylenediamine melamine resin by one pot way, the coating of tetraoxalyl ethylenediamine melamine resin at multiwalled carbon nanotubes (MWCNTs), and the determination of Ni(II). The present materials were carefully examined by Fourier transform infrared spectroscopy, field emission scanning electron microscope, and electrochemistry techniques. A great deal of amorphous microsphere could be observed for tetraoxalyl ethylenediamine melamine resin with an average diameter of 1.2 μm, and MTE could evenly adhere at the surface of MWCNTs by the ultrasonic. Tetraoxalyl ethylenediamine melamine resin-coated multiwalled carbon nanotube-modified paraffin-impregnated graphite electrode was successfully used for the determination of Ni(II) by differential pulse adsorptive anodic stripping voltammetry. The current responses (?0.3 V) were linearly increased depending on the concentration from 1?×?10^?11 to 3?×?10^?10 M (i (μA)?=?11.1?+?7.9 c (1?×?10^?12 M); R?=?0.9901, 3σ?=?7?×?10^?12 M).     

A fast and sensitive nanosensor based on MgO nanoparticle room-temperature ionic liquid carbon paste electrode for determination of methyldopa in pharmaceutical and patient human urine samples

In this study, we describe an ionic liquid–MgO nanoparticle modified carbon paste electrode (MgO/NPs/IL/CPE) was used as a simple, fast, and sensitive tool for the investigation of the electrochemical oxidation of methyldopa (MDOP) using voltammetric methods. The MgO/NPs was characterized with different methods such as TEM, SEM, and XRD. The oxidation peak potential of the MDOP at a surface of MgO/NPs/IL/CPE appeared at 450 mV that was about 100 mV lower than the oxidation peak potential at the surface of the traditional carbon paste electrode (CPE) under similar conditions. The electro-oxidation of MDOP occurred in a pH-dependent 2e^? and 2H⁺ process, and the electrode reaction followed a diffusion-controlled pathway. Under optimal conditions at pH 7.0, the anodic peak currents increased linearly with the concentration of MDOP in the range of 0.08–380 μmol L^?1 with a detection limit of 0.03 μmol L^?1 (3σ). The proposed sensor was successfully applied to the determination of MDOP in real samples such as drug and urine.     

Sensitive voltammetric determination of diclofenac using room-temperature ionic liquid-modified carbon nanotubes paste electrode

An ionic liquid-modified carbon nanotubes paste electrode (IL/CNTPE) has been fabricated using hydrophilic ionic liquid (n-hexyl-3-methylimidazolium hexafluoro phosphate) as a binder. This electrode showed enhanced electrochemical response and strong analytical activity towards the direct electrochemical oxidation of diclofenac (DCF). The electron transfer coefficient, α, and charge transfer resistance (R _ct) of DCF at the modified electrode were calculated. Under optimal conditions at pH 7.0, the anodic peak currents increased linearly with the concentration of DCF in the range of 0.5–300 μmol L^?1 with a detection limit of 0.2 μmol L^?1 (3σ). The interferences of foreign substances were investigated. Differential pulse voltammetry was used to check the applicability of the proposed sensor to the determination of DCF in real samples with satisfactory results.     

Electrocatalytic determination of sulfite using a modified carbon nanotubes paste electrode: application for determination of sulfite in real samples

This paper introduces a carbon paste electrode modified with ferrocene and carbon nanotubes as a voltammetric sensor for determination of sulfite at pH 7.0. The results showed that under the optimum condition (pH 7.0) in cyclic voltammetry, the oxidation of sulfite occurred at a potential about 280?mV less positive than the unmodified carbon paste electrode. Kinetic parameters such as electron transfer coefficient (??) and heterogeneous rate constant (k) for sulfite were also determined using electrochemical approaches. Under the optimized conditions, the electrocatalytic oxidation peak current of sulfite showed two linear dynamic ranges with a detection limit of 0.1???M for sulfite. The proposed method was examined as a selective, simple, and precise method for voltammetric determination of sulfite in some real samples such as weak liquor from wood and paper industry, boiler water, river water, industrial water, and tap water.     

Voltammetric determination of hydroxylamine in water samples using a 1-benzyl-4-ferrocenyl-1H-[1,2,3]-triazole/carbon nanotube-modified glassy carbon electrode

A modified glassy carbon electrode has been constructed using a 1-benzyl-4-ferrocenyl-1H-[1,2,3]-triazole along with multiwalled carbon nanotubes. The electrochemical behaviour of modified electrode has been investigated by cyclic voltammetry. Electrocatalytic activity of the modified electrode was investigated for the oxidation of hydroxylamine in 0.1 M phosphate-buffered solution of pH 8. The modified electrode showed electrocatalytic response to the oxidation of hydroxylamine at the potential of 330 mV. The linear range and detection limit for the detection of hydroxylamine in the optimum condition were found to be 4.0?×?10^?7 to 6.75?×?10^?4 M and 28.0?±?1.0 nM, respectively. Finally, the method was employed for the determination of hydroxylamine in water samples.     

Nitrobenzene electrochemical sensor based on silver nanoparticle supported on poly-melamine functional multi-walled carbon nanotube

A novel and convenient electrochemical sensor, based on multi-walled carbon nanotube (MWCNT)–poly-melamine(PMel)–silver nanoparticle (AgNP) composite-modified glassy carbon electrode (GCE), was fabricated for the determination of nitrobenzene (NB). The modified electrode not only played an efficient electrocatalytic role for the reduction of NB but also significantly reduced the overpotential of NB, and the peak current increased greatly compared with bare GCE or other modified electrodes. The excellent performance of NB sensor can be ascribed to the synergistic effect between MWCNT and AgNP. The synergistic effect promoted the electron transfer between MWCNT and AgNP significantly and enhanced the electrochemical reduction ability of NB remarkably. Besides, PMel has huge nitrogen and amine groups, which contributes to the dispersion of silver nanoparticles and also improves the electrocatalytic activity and sensitivity of the sensor. The integration of PMel/MWCNT with AgNP provided a high-performance platform for the NB determination. Under the optimized experimental conditions, the developed sensor showed a wide linear calibration ranges from 20 to 1000 μM and from 1000 to 6000 μM, with a low detection limit (0.55 μM) for the detection of NB. At the same time, the modified electrode exhibited good stability and reproducibility and acceptable selectivity. Moreover, the proposed sensors were successfully employed to determine NB in real samples, and the recoveries were between 97.2 and 104.6 %.     

Sensitive and selective electrochemical sensor for magnolol based on the enhancement effect of multiwalled carbon nanotubes

Herein, insoluble multiwalled carbon nanotubes (MWNTs) were dispersed into N,N-dimethylformamide (DMF) via ultrasonication, resulting in a stable and homogeneous MWNTs suspension. After evaporation of DMF, the surface of glassy carbon electrode was successfully coated with MWNTs film, as confirmed from scanning electron microscopy measurements. In pH 7 phosphate buffer, an irreversible oxidation peak was observed for magnolol, and the peak currents greatly increased on MWNTs film surface. The influences of pH value, amount of MWNTs and accumulation conditions were studied. Based on the remarkable enhancement effect of MWNTs, a new electrochemical sensor with high sensitivity was developed for magnolol. The linear range was from 5 μg?L^?1 to 1 mg?L^?1, and the detection limit was 2 μg?L^?1 (7.51?×?10^?9?M) after a 3-min accumulation. This novel sensor was successfully used to detect the content of magnolol in Chinese traditional medicines, and the recovery was over the range from 98.1 to 99.1 %.     

Synthesis of Water Dispersible Fluorescent Carbon Nanocrystals from <Emphasis Type="Italic">Syzygium cumini</Emphasis> Fruits for the Detection of Fe<Superscript>3+</Superscript> Ion in Water and Biological Samples and Imaging of <Emphasis Type="Italic">Fusarium avenaceum</Emphasis> Cells

In this work, water dispersible fluorescent carbon nanocrystals (NCs) were synthesized by a simple, green and low cost hydrothermal method using Syzygium cumini (jamun) as a carbon source at 180 °C for 6 h. The average size of carbon NCs was found to be 2.1 ± 0.5 nm and shown bright blue fluorescence when excited at 365 nm under UV lamp. The carbon NCs were characterized by spectroscopic (UV-visible and fluorescence, Fourier transform infrared and dynamic light scattering) and high resolution transmission electron microscopic techniques. The quantum yield of carbon NCs was found to be ~5.9 % at 438 nm emission wavelength when excited at 360 nm. It was noticed that none of the metal ions quenched the fluorescence intensity of carbon NCs at 438 nm except for Fe³⁺, indicating the formation of Fe³⁺ ion-carbon NCs complexes. The linear range was observed in the concentration range of 0.01–100 μM with the corresponding detection limits of 0.001 μM, respectively. Furthermore, the carbon NCs were used as probes for imaging of fungal (Fusarium avenaceum) cells.