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In this study, we report the electrochemical detection of sunset yellow (SY) at the surface of a carbon paste electrode (CPE) modified with CuCo2O4 nanorods (NRs) and an ionic liquid (IL). The electrochemical behavior of sunset yellow at the modified electrode was investigated using linear sweep voltammetry, differential pulse voltammetry and chrono­amperometry techniques. The CuCo2O4 NRs/IL/CPE sensor exhibited good performance and favorable electrochemical response for the electrochemical reaction of SY in a 0.1 M phosphate buffer solution at pH 7.0. The results showed a linear electrochemical response to SY within the concentration range of 0.2 to 160.0 μM, with a detection limit of 0.06 μM. In addition, The CuCo2O4 NRs/IL/CPE sensor demonstrated good ability for SY determination in real samples.

Acetylcholine (ACH) is one of the excitatory neurotransmitter in the human body. It is the most abundant neurotransmitter responsible for triggering the activation of postsynaptic neurons, leading to an excitatory response. ACH plays a crucial role in various physiological processes, including muscle contraction, autonomic nervous system regulation, and cognitive functions such as learning and memory. In this study, an electrochemical sensor was prepared based on WO3 nanorods modified glassy carbon electrode for the detection of ACH. The WO3 nanorods provided excellent properties for the electrochemical determination of ACH. The proposed sensor exhibited a wide linear detection range of (0.1 to 400.0 µM) and a low detection limit of 0.025 µM for ACH. These results demonstrate the sensor's high sensitivity in detecting this important neurotransmitter. In addition the developed sensor showed good ability for ACH determination in real samples. This study offers an innovative strategy for the electrochemical detection of ACH, showcasing the potential of nanomaterials in the development of advanced sensing technologies.

Background and purpose: Methotrexate (MTX) is a widely used anti-cancer drug, but its overuse can lead to significant side effects. Therefore, it is very vital to design simple and sensitive analytical methods for its determi­na­tion. Experimental approach: In this work, an electrochemical sensor was prepared based on an ionic liquid (IL)/Ni-Co layered double hydroxide nanosheets (Ni-Co-LDH)-modified carbon paste electrode IL/Ni-Co-LDH/CPE. Cyclic voltammetry, differential pulse voltammetry, and chronoamperometry methods were applied to evaluate the performance of the designed sensor for MTX determination. Key results: The IL/Ni-Co-LDH/CPE sensor exhibits a linear relationship between the peak current of the differential pulse voltammetry and MTX concentrations in the linear dynamic range of 0.02 to 140.0 µM, with a detection limit of 0.006 µM. The IL/Ni-Co-LDH/CPE sensor exhibited relative standard deviation values between 1.7 to 3.7 % for recovery tests on real samples, indicating the precision of the method. Conclusion: The designed sensor with cost-effective and good performance could be valuable for therapeutic drug monitoring and clinical diagnostics.

In this work, we developed a simple technique to produce an effective electrode material consisting of nickel-cobalt-layered double hydroxide/multi-walled carbon nanotubes nanocomposite (Ni-Co-LDH/MWCNTs). This nanocomposite was prepared and characterization techniques such as field-emission scanning electron microscopy (FE-SEM), Fourier-transform infrared (FT-IR) and x-ray powder diffraction (XRD) were used to characterize its morphology and structure. The electrochemical studies and measurements were carried out by using various techniques including cyclic voltammetry (CV), differential pulse voltammetry (DPV), and chronoamperometry (CHA). The Ni-Co-LDH/MWCNTs nanocomposite-modified carbon paste electrode (Ni-Co-LDH/MWCNTs/CPE) exhibited enhanced electrocatalytic performance for the determination of 4-aminophenol. Detection of 4-aminophenol was done by using DPV. According to the results of DPV, the Ni-Co-LDH/MWCNTs/CPE sensor demonstrated a linear response to 4-aminophenol in the linear range of 0.02–700.0 µM, with a limit of detection (LOD) of 0.01 µM, and a sensitivity of 0.076 µA/µM. Also, the modified CPE presented reproducible and repeatable responses to determine 4-AP. The prepared sensor was also applied for determination of 4-aminophenol in the presence of possible interfering species and good results were obtained. In addition, the sensor successfully detected 4-aminophenol in real water samples with recoveries ranging from 98.0 % to 104.0 %, and with relative standard deviation (RSD) below 3.3 %. Therefore, the obtained results indicate that the prepared sensor can be an effective tool for the simple, fast, and sensitive detection of 4-aminophenol in water samples.

Water pollution with phenolic compounds is a serious environmental issue that can pose a major threat to the water sources. This pollution can come from various agricultural and industrial activities. Phenolic compounds can have detrimental effects on both human health and the environment. Therefore, it is essential to develop and improve analytical methods for determination of these compounds in the water samples. In this work, the aim was to design and develop an electrochemical sensing platform for the determination of 2,4-dichlorophenol (2,4-DCP) in water samples. In this regard, a nanocomposite consisting of CoWO4 nanoparticles (NPs) anchored on reduced graphene oxide nanosheets (rGO NSs) was prepared through a facile hydrothermal method. The formation of the CoWO4/rGO nanocomposite was confirmed via different characterization techniques. Then, the prepared CoWO4/rGO nanocomposite was used to modify the surface of a screen-printed carbon electrode (SPCE) for enhanced determination of 2,4-DCP. The good electrochemical response of the modified SPCE towards the oxidation of 2,4-DCP was observed by using cyclic voltammetry (CV) due to the good properties of CoWO4 NPs and rGO NSs along with their synergistic effects. Under optimized conditions, the CoWO4/rGO/SPCE sensor demonstrated a broad linear detection range (0.001 to 100.0 µM) and low limit of detection (LOD) (0.0007 µM) for 2,4-DCP determination. Also, the sensitivity of CoWO4/rGO/SPCE for detecting 2,4-DCP was 0.3315 µA/µM. In addition, the good recoveries for determining spiked 2,4-DCP in the water samples at the surface of CoWO4/rGO/SPCE showed its potential for determination of this compound in real samples.

Background and purpose: Neurotransmitters are chemical messengers that enhance and balance signals between cells and target cells in the body. They are vital to the body's ability to function. Epinephrine is one of the most essential catecholamine neurotransmitters with an important biological and pharmacological role in the mammalian central nervous system. Therefore, it is very important to develop sensitive, simple, and fast methods for the determination of this compound. Experimental approach: In the present work, a glassy carbon electrode (GCE) modified with the cerium oxide-zinc oxide (CeO2-ZnO) nanocomposite (CeO2-ZnO/GCE) was developed for the sensitive and quick detection of epinephrine. The CeO2-ZnO nanocom­posite was prepared by hydrothermal method. Electrochemical methods such as voltammetry and chrono­ampero­metry techniques were used to investigate the performance of the developed sensor. Key results: The resulting CeO2-ZnO/GCE showed a remarkable response towards the determination of epinephrine. The electrochemical sensor demonstrated a wide dynamic linear range from 0.1 to 900.0 μM for analysis of epinephrine. The LOD equalled 0.03 μM for epinephrine. In addition, the electrochemical sensor had good feasibility for concurrent detection of epinephrine and theophylline. Furthermore, experimental outputs indicated that the oxidation peaks of epinephrine and theophylline were separated by a 685 mV difference between the two peaks in PBS at a pH of 7.0. Also, an electrochemical sensor has been employed to analyse epinephrine in real samples (urine and epinephrine Injection). Conclusion: The good and acceptable analytical performance of the developed sensor can provide a promising tool for the analysis of epinephrine in real samples.

In the present research, ZnO@TiO2 nanoparticles (ZnO@TiO2 NPs) was synthesized by using a simple method and the results of infrared (IR), X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and energy-dispersive X-ray spectroscopy (EDX) confirmed their synthesis. Then, an electrochemical sensor based on screen printed graphite electrode (SPGE) modified with ZnO@TiO2 NPs was developed for voltammetric detection of hydrazine in water samples. The ZnO@TiO2 NPs modified SPGE demonstrates significant performance toward the hydrazine detection due to the synergistic effect between ZnO NPs and TiO2 NPs and it proved by the results from cyclic voltammetry (CV). Also, the observation of an oxidation peak without a reduction peak in the opposite scan direction indicated the irreversibility of the electrochemical oxidation of hydrazine on both the bare SPGE and the ZnO@TiO2/SPGE. Under optimized conditions (pH and differential pulse parameters), the voltammetric current response of hydrazine at the ZnO@TiO2/SPGE showed linear dependence on the concentration, ranging from 0.01 µM to 585.0 µM with a limit of detection (LOD) of 0.005 µM. In addition, the pertinency of the ZnO@TiO2/SPGE sensor for practical applications was investigated by quantification detection of hydrazine in water samples. The findings showed recovery values between 97.3 % and 104.2 % and relative standard deviations (RSDs) ≤ 3.5 % for river and tap water samples.

In this work, UiO-66-NH2/GO nanocomposite was prepared using a simple solvothermal technique, and its structure and morphology were characterized using field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD). An enhanced electrochemical sensor for the detection of epirubicin (EP) was proposed, which utilized a UiO-66-NH2/GO nanocomposite-modified screen-printed graphite electrode (UiO-66-NH2/GO/SPGE). The prepared UiO-66-NH2/GO nanocomposite improved the electrochemical performance of the SPGE towards the redox reaction of EP. Under optimized experimental conditions, this sensor demonstrates a remarkable limit of detection (LOD) of 0.003 µM and a linear dynamic range from 0.008 to 200.0 µM, providing a highly capable platform for sensing EP. Furthermore, the simultaneous electro-catalytic oxidation of EP and topotecan (TP) was investigated at the UiO-66-NH2/GO/SPGE surface utilizing differential pulse voltammetry (DPV). DPV measurements revealed the presence of two distinct oxidation peaks of EP and TP, with a peak potential separation of 200 mV. Finally, the UiO-66-NH2/GO/SPGE sensor was successfully utilized for the quantitative analysis of EP and TP in pharmaceutical injection, yielding highly satisfactory results.

In this work, the glassy carbon electrode (GCE) surface was modified with nitrogen-doped hollow carbon spheres (N-HCSs) to achieve a new electrochemical sulphite sensor (N-HCSs/GCE) in water samples. The N-HCSs were explored for electrocatalytic behavior through voltammetric approaches using a routine three-electrode system. The findings revealed an admirable efficiency for modified electrodes towards sulphite oxidation, highlighting the effectiveness of our as-produced sulphite sensor. The differential pulse voltammetry was utilized under obtained optimal circumstances to study the as-developed sensor, the results of which underlined linear electrochemical current in relation to sulphite concentration, with dynamic range as wide as 1.0-100.0 μM and limit of detection as narrow as 0.35 μM. Moreover, N-HCSs/GCE had commendable practical applicability for sensing sulphite present in real specimens with voltammetric techniques.

Background and purpose: Sensitive analytical determination of folic acid is important in clinical laboratories due to its versatile biological functions. Experimental approach: A simple folic acid sensor was successfully fabricated based on two-dimensional transition metal dichalcogenide MoS2 modified carbon ionic liquid paste electrode (MoS2-CILPE). The electrochemical properties of the fabricated electrode were investigated by cyclic voltammetry (CV), differential pulse voltammetry (DPV), and chronoamperometry. Key results: The fabricated sensor displayed excellent electroactivity towards folic acid using CV. Under optimal conditions (0.1 M PBS (pH 7.0)), the DPV oxidation peak current was proportional to folic acid concentration in the range from 5.0 μM to 100.0 μM with an estimated limit of detection of 1.0 µM and limit of quantification of 5.0 µM. Conclusion: The ability of the sensor for routine analyses was demonstrated by the detection of folic acid present in folic acid tablets and urine samples with appreciable recovery values.

D-penicillamine (D-PA) is a sulfur-containing drug that has been used for various health conditions. However, like any medication, overdosing on D-PA can have adverse effects and may require additional treatment. Therefore, developing simple and sensitive methods for sensing D-PA can play a crucial role in improving its efficacy and reducing its side effects. Sensing technologies, such as electrochemical sensors, can enable accurate and real-time measurement of D-PA concentrations. In this work, we developed a novel electrochemical sensor for detecting D-PA by modifying a carbon paste electrode (CPE) with a multi-walled carbon nanotube-Co3O4 nanocomposite, benzoyl-ferrocene (BF), and ionic liquid (IL) (MWCNT-Co3O4/BF/ILCPE). Cyclic voltammetry (CV), differential pulse voltammetry (DPV), and chronoamperometry (CHA) were employed to explore the electrochemical response of D-PA on the developed sensor, the results of which verified a commendable electrochemical performance towards D-PA. Under optimized conditions, the developed sensor demonstrated a rapid response to D-PA with a linear dynamic range of 0.05 μM–100.0 μM, a low detection limit of 0.015 μM, and a considerable sensitivity of 0.179 μA μM−1. Also, the repeatability, stability, and reproducibility of the MWCNT-Co3O4/BF/ILCPE sensor were studied and showed good characteristics. In addition, the detection of D-PA in pharmaceutical and biological matrices yielded satisfactory recoveries and relative standard deviation (RSD) values.

Abstract Acetamiprid removal was investigated by synthesized Graphene oxide, multiwall nanotube and graphite from an aqueous solution. For this propose, FT-IR, XRD, UV–Vis, SEM and EDS were used to characterize the synthesized nano adsorbents and to determine the removal process. A novel PVC membrane electrode as selective electrode made for determining the concentration of acetamiprid. Batch adsorption studies were conducted to investigate the effect of temperature, initial acetamiprid concentration, adsorbent type and contact time as important adsorption parameters. The maximum equilibrium time was found to be 15 min for graphene oxide. The kinetics studies showed that the adsorption of acetamiprid followed the pseudo-second-order kinetics mechnism. All the adsorption equilibrium data were well fitted to the Langmuir isotherm model and maximum monolayer adsorption capacity 99 percent. Docking data of adsorption have resulted in the same as experimental data in good manner and confirmed the adsorption process.

Abstract A novel electrochemical sensing platform was designed and prepared for the simultaneous detection of sumatriptan and naproxen by exploiting the prowess of the Fe3O4@ZIF-8 nanoparticles (NPs); as-synthesized Fe3O4@ZIF-8 NPs were characterized by energy-dispersive X-ray spectroscopy, fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy (FESEM), transmission electron microscopy and thermal gravimetric analysis. The immobilized Fe3O4@ZIF-8 NPs on a screen printed graphite electrode (SPGE) was evaluated electrochemically via cyclic voltammetry, linear sweep voltammetry, and differential pulse voltammetry as well as chronoamprometery means; Fe3O4@ZIF-8/SPGE exhibited good sensing performance for sumatriptan in a range of 0.035–475.0 µM with detection limit of 0.012 µM. Also, Fe3O4@ZIF-8/SPGE exhibited good sensing performance for naproxen in a range of 0.1–700.0 µM with detection limit of 0.03 µM. The modified electrode showed two separate oxidative peaks at 620 mV for sumatriptan and at 830 mV for naproxen with a peak potential separation of 210 mV which was large enough to detect the two drugs simultaneously besides being stable in the long-run with considerable reproducibility. Real sample analyses were carried out to identify the function of fabricated electrode in sensing applications wherein trace amounts of sumatriptan and naproxen could be identified in these samples.

A new voltammetric sensor is proposed for the determination of bisphenol A, using a glassy carbon electrode (GCE) modified with Fe3O4/graphene oxide (GO) nanocomposite. The modification of the electrode surface was performed by dispersion drop-casting. The electro­chemical behavior of bisphenol A was evaluated by cyclic voltammetry (CV). The oxidation peak was observed during the anodic potential scan at potentials of 0.45 V. Higher anodic peak currents (Ipa) were observed at Fe3O4/GO/GCE modified electrode than at bare GCE. The elec­trochemical determination by differential pulse voltammetry (DPV) revealed a linear response in the concentration range of 1.0×10-7 to 5.0×10-5 M, with a detection limit of 9.0×10-8 M. The proposed method was successfully applied using water samples, with good recoveries.

This study addressed the use of manganese dioxide nanorods/graphene oxide nanocomposite (MnO2 NRs/GO) for modifying a glassy carbon electrode (GCE). The modified electrode (MnO2 NRs/GO/GCE) was used as an electrochemical sensor for the determination of hydroquinone (HQ) in water samples. Differential pulse voltammetry (DPV), cyclic voltammetry (CV), and chronoamperometry were used for more analysis of the HQ electrochemical behavior. Analyses revealed acceptable electrochemical functions with lower transfer resistance of electrons and greater conductivity of the MnO2 NRs/GO/GCE. The small peak-to-peak separation is an indication of a rapid electron transfer reaction. Therefore, this result is probably related to the effect of the MnO2 NRs/GO nanocomposite on the surface of GCE. In the concentration range of 0.5 μM to 300.0 μM with the detection limit as 0.012 μM, there was linear response between concentration of HQ and the current. The selectivity of the modified electrode was determined by detecting 50.0 μM of HQ in the presence of various interferent molecules. At the end, the results implied the acceptable outcome of the prepared electrode for determining HQ in the water samples.

In this work, we prepared a novel electrochemical sensor for the detection of tramadol based on a UiO-66-NH2 metal–organic framework (UiO-66-NH2 MOF)/third-generation poly(amidoamine) dendrimer (G3-PAMAM dendrimer) nanocomposite drop-cast onto a glassy carbon electrode (GCE) surface. After the synthesis of the nanocomposite, the functionalization of the UiO-66-NH2 MOF by G3-PAMAM was confirmed by various techniques including X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), field emission-scanning electron microscopy (FE-SEM), and Fourier transform infrared (FT-IR) spectroscopy. The UiO-66-NH2 MOF/PAMAM-modified GCE exhibited commendable electrocatalytic performance toward the tramadol oxidation owing to the integration of the UiO-66-NH2 MOF with the PAMAM dendrimer. According to differential pulse voltammetry (DPV), it was possible to detect tramadol under optimized circumstances in a broad concentration range (0.5 μM–500.0 μM) and a narrow limit of detection (0.2 μM). In addition, the stability, repeatability, and reproducibility of the presented UiO-66-NH2 MOF/PAMAM/GCE sensor were also studied. The sensor also possessed an acceptable catalytic behavior for the tramadol determination in the co-existence of acetaminophen, with the separated oxidation potential of ΔE = 410 mV. Finally, the UiO-66-NH2 MOF/PAMAM-modified GCE exhibited satisfactory practical ability in pharmaceutical formulations (tramadol tablets and acetaminophen tablets).

The purpose of the present study was to introduce a newly designed approach for determi­nation of glutathione using modified carbon paste electrode with ZnFe2O4 nanoparticles, ionic liquid (1-butyl-3-methylimidazolium hexafluorophosphate) and ethyl 2-(4-ferrocenyl-[1,2,3]triazol-1-yl)acetate (EFTA/ZFO/IL/CPE). According to the results from the electro­chemical experiments, oxidation current of glutathione on the modified electrode surface was incremented and its oxidation was decreased compared to bare CPE. A linear response was observed for the electrode at different methyldopa concentrations (0.2 to 300.0 μM).

Editorial

T This research applied a nanostructured electrochemical sensor with a screen-printed electrode (SPE) for examining the dopamine (DA) electrocatalytic oxidation when uric acid (UA) was present. Cu(salophen) nanostructured modified SPE Cu(salophen)/SPE was employed to investigate the electrochemical behavior of DA. At optimal pH (pH 7.0), oxidation of DA at the modified electrode takes place at a potential around 100 mV less positive than at the unmodified SPE. Chronoamperometry was used to determine the diffusion coefficient of DA (D = 1.96×10-5 cm2 s-1). Differential pulse voltammetry (DPV) showed linear response in the range between 0.2-450.0 μM for DA. The limit of detection (LOD) of DA was computed to be 0.05 μM. Moreover, Cu(salophen)/SPE was employed for determining DA in the presence of UA using DPV. The DPV results showed that at the modified electrode, two well-separated oxidation peaks of DA and UA could be obtained at potentials of 180 and 325 mV, respectively. This separation forms the basis for the co-detection of these two materials on the surface of Cu(salophen)/SPE. This sensor was then employed to determine DA and UA in real specimens.

We constructed two-dimensional NiCo-metal–organic-framework (NiCo-MOF) nanosheets based on a facile protocol and then characterized them using multiple approaches (X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), field emission-scanning electron microscopy (FE-SEM), and N2 adsorption/desorption isotherms techniques). As a sensitive electroactive material, the as-fabricated bimetallic NiCo-MOF nanosheets were employed to modify a screen-printed graphite electrode surface (NiCo-MOF/SPGE) for epinine electro-oxidation. According to the findings, there was a great improvement in the current responses of the epinine because of the appreciable electron transfer reaction and catalytic performance of the as-produced NiCo-MOF nanosheets. Differential pulse voltammetry (DPV), cyclic voltammetry (CV) and chronoamperometry were utilized to analyze the electrochemical activity of the epinine on the NiCo-MOF/SPGE. A linear calibration plot was obtained in the broad concentration range (0.07–335.0 µM) with a high sensitivity (0.1173 µA/µM) and a commendable correlation coefficient (0.9997). The limit of detection (S/N = 3) was estimated at 0.02 µM for the epinine. According to findings from DPV, the electrochemical sensor of the NiCo-MOF/SPGE could co-detect epinine and venlafaxine. The repeatability, reproducibility and stability of the NiCo-metal–organic-framework-nanosheets-modified electrode were investigated, and the relative standard deviations obtained indicated that the NiCo-MOF/SPGE had superior repeatability, reproducibility and stability. The as-constructed sensor was successfully applicable in sensing the study analytes in real specimens.

In this paper, a simple strategy was proposed for the analysis of catechol by a carbon paste electrode (CPE) modified with graphene oxide–third generation of poly(amidoamine) dendrimer (GO/G3–PAMAM) nanocomposite and ionic liquid (IL). The synthesis of GO–PAMAM nanocomposite was confirmed using X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), field emission scanning electron microscopy (FE-SEM), and Fourier transform infrared spectroscopy (FT-IR) techniques. The prepared modified electrode (GO–PAMAM/ILCPE) exhibited good performance to detect catechol with a notable decrease in overpotential and increase in current compared with an unmodified CPE. Under optimum experimental conditions, GO–PAMAM/ILCPE electrochemical sensors indicated a lower limit of detection (LOD) of 0.034 μM and a linear response in the concentration range of 0.1 to 200.0 µM for the quantitative measurement of catechol in aqueous solutions. In addition, GO–PAMAM/ILCPE sensor exhibited an ability to simultaneously determine catechol and resorcinol. It can be found that catechol and resorcinol could be completely separated on the GO–PAMAM/ILCPE with the differential pulse voltammetry (DPV) technique. Finally, a GO–PAMAM/ILCPE sensor was utilized to detect catechol and resorcinol in water samples with recoveries of 96.2% to 103.3% and relative standard deviations (RSDs) of less than 1.7%.

Recently, transition metal oxides have been considered for various applications due to their unique properties. We present the synthesis of a three-component catalyst consisting of zirconium oxide (ZrO2), nickel oxide (NiO), and reduced graphene oxide (rGO) in the form of ZrO2/NiO/rGO by a simple one-step hydrothermal method. X-ray powder diffraction (XRD), scanning electron microscope (SEM), and bright-field transmission electron microscopy (BF-TEM) analyses were performed to accurately characterize the catalysts. Cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and linear sweep voltammetry (LSV) analyses were also carried out to investigate the methanol and ethanol alcohol electrooxidation ability of the synthesized nanocatalysts. Inspired by the good potential of metal oxides in the field of catalysts, especially in fuel-cell anodes, we investigated the capability of this catalyst in the methanol oxidation reaction (MOR) and ethanol oxidation reaction (EOR). After proving the successful synthesis and examining the surface morphology of these materials, detailed electrochemical tests were performed to show the outstanding capability of this new nanocatalyst for use in the anode of alcohol fuel cells. ZrO2/NiO/rGO indicated a current density of 26.6 mA/cm2 at a peak potential of 0.52 V and 99.5% cyclic stability in the MOR and a current density of 17.3 mA/cm2 at a peak potential of 0.52 V and 98.5% cyclic stability in the EOR (at optimal concentration/scan rate 20 mV/s), representing an attractive option for use in the anode of alcoholic fuel cells.

The current attempt was made to detect the amino acid homocysteine (HMC) using an electrochemical aptasensor. A high-specificity HMC aptamer was used to fabricate an Au nanostructured/carbon paste electrode (Au-NS/CPE). HMC at high blood concentration (hyperhomocysteinemia) can be associated with endothelial cell damage leading to blood vessel inflammation, thereby possibly resulting in atherogenesis leading to ischemic damage. Our proposed protocol was to selectively immobilize the aptamer on the gate electrode with a high affinity to the HMC. The absence of a clear alteration in the current due to common interferants (methionine (Met) and cysteine (Cys)) indicated the high specificity of the sensor. The aptasensor was successful in sensing HMC ranging between 0.1 and 30 μM, with a narrow limit of detection (LOD) as low as 0.03 μM.

Folic acid (FA) as one of the water‐soluble vitamins contributes to the construction of healthy cells, as FA deficiency is one of the leading causes of anaemia. Based on reports, reduced folate level can lead to development of carcinogenesis. Hence, its analysis from the clinical point of view is highly demanded. In the present work, NiFe2O4 nanoparticles was successfully synthesized and used for modified novel voltammetric sensor for determination of folic acid. Differential pulse voltammetry response shows the linear increment of oxidation signals with an increase in the concentration of folic acid in the range of 1.0 × 10-7-5.0 × 10-4 M with limit of detection 3.4 × 10-8 M. The modified electrode displays an excellent selectivity towards the determination of FA even in the presence of various interfering species. Finally, the screen printed electrode (SPE) consists of three main parts which are a graphite counter electrode, a silver pseudo-reference electrode and a graphite working electrode modified by NiFe2O4 nanoparticles (NFO) was applied for FA determination folic acid tablet and urine samples whose accuracy was attested by means of addition and recovery assays (97.0-103.5%) as well as by differential pulse voltammetry.

Nitrogen (N) doping is a well-known approach that can be effectively used to tune the properties of graphene-supported materials. The current attempt followed a simple hydrothermal protocol for the fabrication of N-doped graphene sheets (N-GSs). The N-GSs were subsequently applied to modify the surface of a glassy carbon electrode (GCE) for a dopamine (DA) electrochemical sensor (N-GSs/GCE), tested on the basis of differential pulse voltammetry (DPV). The findings highlighted a limit of detection (LOD) as narrow as 30 nM and a linear response in the concentration range between 0.1 and 700.0 μM. The modified electrode could successfully determine DA in the co-existence of uric acid (UA) and ascorbic acid (AA), the results of which verified the potent electrocatalytic performance of the proposed sensor towards AA, DA, and UA oxidation, and three distinct voltammetric peaks at 110, 250, and 395 mV via DPV. The practical applicability of the as-developed N-GSs/GCE sensor was confirmed by sensing the study analytes in real specimens, with satisfactory recovery rates.

The current work was performed to construct a novel electrochemical sensing system for determination of sunset yellow via the modification of screen-printed graphite electrode modified with hierarchical flower-like NiCo2O4 nanoplates (NiCo2O4/SPGE). The prepared material (hierarchical flower-like NiCo2O4 nanoplates) was analyzed by diverse microscopic and spectroscopic approaches for the crystallinity, composition, and morphology. Chronoamperometry, differential pulse voltammetry, linear sweep voltammetry, and cyclic voltammetry were used for determination of the electrochemical behavior of sunset yellow. The as-fabricated sensor had appreciable electro-catalytic performance and current sensitivity in detecting the sunset yellow. There were some advantages for NiCo2O4/SPGE under the optimized circumstances of sunset yellow determination, including a broad dynamic linear between 0.02 and 145.0 µM, high sensitivity of 0.67 μA/(μM.cm2), and a narrow limit of detection of 0.008 μM. The practical applicability of the proposed sensor was verified by determining the sunset yellow in real matrices, with satisfactory recoveries.

A chemically modified carbon paste electrode, based on a CoMOF-graphene oxide (GO) and an ionic liquid of 1-methyl-3-butylimidazolium bromide (CoMOF-GO/1-M,3-BB/CPE), was fabricated for the simultaneous determination of dopamine (DA) and uric acid (UA). The prepared CoMOF/GO nanocomposite was characterized by field emission-scanning electron microscopy (FE-SEM), the X-ray diffraction (XRD) method, a N2 adsorption–desorption isotherm, and an energy dispersive spectrometer (EDS). The electrochemical sensor clearly illustrated catalytic activity towards the redox reaction of dopamine (DA), which can be authenticated by comparing the increased oxidation peak current with the bare carbon paste electrode. The CoMOF-GO/1-M,3-BB/CPE exhibits a wide linear response for DA in the concentration range of 0.1 to 300.0 µM, with a detection limit of 0.04 µM. The oxidation peaks’ potential for DA and uric acid (UA) were separated well in the mixture containing the two compounds. This study demonstrated a simple and effective method for detecting DA and UA in real samples.

In this work, Ni-Co layered double hydroxide (Ni–Co LDH) hollow nanostructures were synthesized and characterized by X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), and Fourier-transform infrared spectroscopy (FT-IR) techniques. A screen-printed electrode (SPE) surface was modified with as-fabricated Ni–Co LDHs to achieve a new sensing platform for determination of sumatriptan. The electrochemical behavior of the Ni–Co LDH-modified SPE (Ni-CO LDH/SPE) for sumatriptan determination was investigated using voltammetric methods. Compared with bare SPE, the presence of Ni-Co LDH was effective in the enhancement of electron transport rate between the electrode and analyte, as well as in the significant reduction of the overpotential of sumatriptan oxidation. Differential pulse voltammetry (DPV) was applied to perform a quantitative analysis of sumatriptan. The linearity range was found to be between 0.01 and 435.0 μM. The limits of detection (LOD) and sensitivity were 0.002 ± 0.0001 μM and 0.1017 ± 0.0001 μA/μM, respectively. In addition, the performance of the Ni-CO LDH/SPE for the determination of sumatriptan in the presence of naproxen was studied. Simultaneous analysis of sumatriptan with naproxen showed well-separated peaks leading to a quick and selective analysis of sumatriptan. Furthermore, the practical applicability of the prepared Ni-CO LDH/SPE sensor was examined in pharmaceutical and biological samples with satisfactory recovery results.

This work focuses on the development of a novel electrochemical sensor for the determination of morphine in the presence of diclofenac. The facile synthesis of graphene-Co3O4 nanocomposite was performed. The prepared material (graphene-Co3O4 nanocomposite) was analyzed by diverse microscopic and spectroscopic approaches for its crystallinity, composition, and morphology. Concerning the electrochemical determinations, after drop-casting the as-fabricated graphene-Co3O4 nanocomposite on the surface of a screen-printed graphite electrode (SPGE), their electrochemical performance was scrutinized towards the morphine detection. It was also found that an SPGE modified by a graphene-Co3O4 nanocomposite exhibited better electrocatalytic activity for morphine oxidation than unmodified electrode. Under optimal conditions, the differential pulse voltammetry (DPV) was employed to explore the present sensor (graphene-Co3O4/SPGE), the findings of which revealed a linear dynamic range as broad as 0.02–575.0 µM and a limit of detection (LOD) as narrow as 0.007 μM. The sensitivity was estimated to be 0.4 µM/(µA cm2). Furthermore, the graphene-Co3O4/SPGE sensor demonstrated good analytical efficiency for sensing morphine in the presence of diclofenac in well-spaced anodic peaks. According to the DPV results, this sensor displayed two distinct peaks for the oxidation of morphine and diclofenac with 350 mV potential difference. In addition, the graphene-Co3O4/SPGE was explored for voltammetric determination of diclofenac and morphine in pharmaceutical and biological specimens of morphine ampoule, diclofenac tablet, and urine, where recovery rates close to 100% were recorded for all of the samples.

A highly sensitive electrochemical sensor was fabricated based on ionic liquid and NiFe2O4 nanoparticles modified carbon paste electrode for determination of mangiferin. The modified electrode exhibited excellent electrocatalytic activity towards the oxidations mangiferin in phosphate buffer solution (pH 7.0). Cyclic voltammetry (CV), chronoamperometry (CHA) and differential pulse voltammetry (DPV) were used to investigate the electrochemical reaction of mangiferin at the modified electrode. It dramatically enhanced mangiferin oxidation current and shifted its potential towards less positive potential when compared to bare CPE. The peak current vs. mangiferin concentration diagram was found to be linear in range of 0.1 to 500.0 μM with the respective slope of 0.0576 μA μM-1. The detection limit obtained by DPV was 0.09 μM (S/N = 3). The proposed sensor was proved to be applicable for the determination of the mangiferin in urine samples.

In this work, we develop an electrochemical sensor using a polypyrrole nanotubes-modified graphite screen-printed electrode (PPy NTs/GSPE) for sensing hydroxylamine. The PPy NTs/GSPE-supported sensor has an appreciable electrocatalytic performance and great stability for hydroxylamine oxidation. Compared to a bare graphite screen-printed electrode, we demonstrate that using the PPy NTs/GSPE leads to a significant reduction in the oxidation potential of hydroxylamine. The standard curve shows a linear relationship ranging from 0.005 to 290.0 μM (R2 = 0.9998), with a high sensitivity (0.1349 μA/μM) and a narrow limit of detection (LOD) of 0.001 μM. In addition, the PPy NTs/GSPE has satisfactory outcomes for hydroxylamine detection in real specimens.

The current work introduced a convenient single-phase hydrothermal protocol to fabricate MnO2 nanorods (MnO2 NRs). Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), Energy-dispersive X-ray spectroscopy (EDX) and field-emission scanning electron microscopy (FE-SEM) were used to determine the characteristics of MnO2 NR. Then, ionic liquid (IL) and MnO2 NRs were utilized to modify a carbon paste electrode (CPE) surface (MnO2NR-IL/CPE) to voltammetrically sense the sulfanilamide (SAA). An enhanced voltammetric sensitivity was found for the as-developed modified electrode toward SAA when compared with a bare electrode. The optimization experiments were designed to achieve the best analytical behavior of the SAA sensor. Differential pulse voltammetry (DPV) in the optimized circumstances portrayed a linear dependence on various SAA levels (between 0.07 and 100.0 μM), possessing a narrow detection limit (0.01 μM). The ability of the modified electrode to be used in sensor applications was verified in the determination of SAA present in the actual urine and water specimens, with impressive recovery outcomes.

Many studies have addressed electrochemical biosensors because of their simple synthesis process, adjustability, simplification, manipulation of materials’ compositions and features, and wide ranges of detection of different kinds of biomedical analytes. Performant electrochemical biosensors can be achieved by selecting materials that enable faster electron transfer, larger surface areas, very good electrocatalytic activities, and numerous sites for bioconjugation. Several studies have been conducted on the metal–organic frameworks (MOFs) as electrode modifiers for electrochemical biosensing applications because of their respective acceptable properties and effectiveness. Nonetheless, researchers face challenges in designing and preparing MOFs that exhibit higher stability, sensitivity, and selectivity to detect biomedical analytes. The present review explains the synthesis and description of MOFs, and their relative uses as biosensors in the healthcare sector by dealing with the biosensors for drugs, biomolecules, as well as biomarkers with smaller molecular weight, proteins, and infectious disease.

In this paper, graphene (Gr)/Co3O4 nanocomposite was synthesized and utilized for the development of a novel electrochemical sensor to detect tramadol. Tramadol determination was examined by linear sweep voltammetry, differential pulse voltammetry, cyclic voltammetry, and chronoamperometry on Gr/Co3O4 nanocomposite-modified screen-printed electrode (Gr/Co3O4/SPE) in phosphate-buffered saline (PBS). Under the optimized condition, the detection limit of tramadol is 0.03 μM (S/N = 3) in the linear ranges of 0.1–500.0 μM. Furthermore, Gr/Co3O4/SPE was satisfactorily utilized to detect tramadol in tramadol tablet and urine specimens.

We used MoS2 nanosheets (MoS2 NSs) for surface modification of screen-printed electrode (MoS2NSs-SPE) aimed at detecting isoniazid (INZ) in the presence of acetaminophen (AC). According to analysis, an impressive catalytic performance was found for INZ and AC electro-oxidation, resulting in an appreciable peak resolution (~320 mV) for both analytes. Chronoamperometry, differential pulse voltammetry (DPV), linear sweep voltammogram (LSV), and cyclic voltammetry (CV) were employed to characterize the electrochemical behaviors of the modified electrode for the INZ detection. Under the optimal circumstances, there was a linear relationship between the peak current of oxidation and the various levels of INZ (0.035–390.0 µM), with a narrow limit of detection (10.0 nM). The applicability of the as-developed sensor was confirmed by determining the INZ and AC in tablets and urine specimens, with acceptable recoveries.

In this study, we prepared graphene oxide (GO)/ZIF-67 nanocomposites. Therefore, GO/ZIF-67 nanocomposites were used as a modifier on a screen-printed electrode (GO/ZIF-67/SPE) for studying the electrochemical behavior of epinine in phosphate buffer saline (PBS) at pH 7.0 with voltammetry techniques. The GO/ZIF-67/SPE showed greater electrocatalytic activities than the bare SPE. As a result, the GO/ZIF-67/SPE was utilized for additional electrochemical examinations. The epinine concentration determination was in the range 9.0 × 10−8 M to 5.0 × 10−4 M, and the limit of detection (LOD) as well as the limit of quantification (LOQ) equaled 2.0 and 6.6 nM, respectively. From the scan rate study, the oxidation of epinine was found to be diffusion-controlled, and the simultaneous detection of epinine and dobutamine were well achieved with the differential pulse voltammetric (DPV) technique. Moreover, the stability and reproducibility of epinine at the GO/ZIF-67/SPE was studied, and the use of the GO/ZIF-67/SPE to detect epinine and dobutamine in real samples was furthermore successfully demonstrated.

We have developed a highly sensitive sensor of ZnFe2O4/reduced graphene oxide (ZnFe2O4/RGO) nanocomposite for electrochemical detection of hydrazine, fabricated by a simple hydrothermal protocol. Subsequently, a screen-printed electrode (SPE) surface was modified with the proposed nanocomposite (ZnFe2O4/RGO/SPE), and revealed an admirable electrocatalytic capacity for hydrazine oxidation. The ZnFe2O4/RGO/SPE sensor could selectively determine micromolar hydrazine concentrations. The as-produced sensor demonstrated excellent ability to detect hydrazine due to the synergistic impacts of the unique electrocatalytic capacity of ZnFe2O4 plus the potent physicochemical features of RGO such as manifold catalytic sites, great area-normalized edge-plane structures, high conductivity, and large surface area. The hydrazine detection using differential pulse voltammetry exhibited a broad linear dynamic range (0.03–610.0 µM) with a low limit of detection (0.01 µM).

Abstract In the present study, a screen-printed electrode based-sensor with electrochemical detection was developed for rapid and sensitive determination of acetylcholine. At first, the screen-printed carbon electrode was modified by using a magnetic core shell and then was used for voltammetric determination of acetylcholine in ampoule, serum and urine samples. The electrochemical behaviour of acetylcholine at the modified electrode was investigated by cyclic voltammetry. The modified electrode displayed a decrease in the overpotential (ca. 130 mV) and an obvious increase in the peak current compared to the non-modified screen-printed electrode. The results indicated that modified screen-printed electrode enhanced electrocatalytic activity towards the oxidation of acetylcholine. Under optimized conditions, the limit of detection from the experiment of acetylcholine determination was 0.02 µM with acetylcholine concentration in range of 0.1–500.0 µM. The reproducibility of the measurements was tested by recording the responses for 50.0 µM acetylcholine with four different developed sensors prepared on the same manner and the same day. A relative standard deviation value of 4.3% was obtained. Finally, a recovery test is done as a part of accuracy evaluation of the system.

We developed a novel hydroxylamine sensor through the surface modification of screen-printed electrode (SPE) with NiCo2O4 nanoparticles/reduced graphene oxide (RGO) nanocomposite (NiCo2O4/RGO/SPE). We assessed the electrochemical response of hydroxylamine on the as-fabricated sensor, confirming the high electrocatalytic impact of hydroxylamine oxidation. The electrode produced sensitively responded to hydroxylamine under optimized conditions, with a low limit of detection (2.0 nM) and broad linear dynamic range (0.007–385.0 µM). The presence of NiCo2O4 combined with the modification of RGO resulted in sensitive detection and signal amplification of hydroxylamine oxidation. The proposed sensor was used to determine the existence of hydroxylamine in water samples.

A chemically modified carbon paste electrode with 2-chlorobenzoyl ferrocene (2CBF) and carbon nanotube (2CBFCNPE) was employed to study the electrocatalytic oxidation of ascorbic acid in aqueous solution using cyclic voltammetry, square wave voltammetry and chronoamperometry. The diffusion coefficient (D = 1.42 × 10-6 cm2 s-1), and the kinetic parameter such as the catalytic rate constant (k = 3.7 × 10 3 M-1 s-1) of ascorbic acid oxidation at the surface of 2CBFCNPE were determined using electrochemical approaches. It has been found that under an optimum condition (pH 4.0), the oxidation of ascorbic acid at the surface of such an electrode occurs at a potential about 85 mV less positive than that of an unmodified carbon paste electrode. Applying square wave voltammetry, in phosphate buffer solution (PBS) of pH 4.0, the oxidation current increases linearly with two concentration intervals of ascorbic acid, one is 1.0 × 10-7-2.5 × 10-6 M and the other is 2.5 × 10-6-7.0 × 10-5 M. Detection limit (3δ) was obtained 64.0 nM. This method was also examined for determination of ascorbic acid in some real samples.

Flower-like La3+/ZnO nanocomposite was facile synthesized. A simple and ultrasensitive sensor based on graphite screen printed electrode (SPE) modified by La3+/ZnO nanoflower was developed for the electrochemical determination of dopamine. The electrochemical behavior of dopamine was studied in 0.1 M phosphate buffer solution (PBS) using cyclic voltammetry (CV), chronoamperometry (CA) and differential pulse voltammetry (DPV). Compared with the unmodified graphite screen printed electrode, the modified electrode facilitates the electron transfer of dopamine, since it notably increases the oxidation peak current of dopamine. Also, according to CV results the maximum oxidation of dopamine on La3+/ZnO/SPE occurs at 150 mV which is about 140 mV more negative compared with unmodified SPE. Under optimized conditions, the modified electrode exhibited a linear response over the concentration range from 0.15 to 300.0 μM, with a detection limit of 0.08 μM (S/N = 3). The proposed sensor exhibited a high sensitivity, good stability and was successfully applied for dopamine determination in dopamine ampoule, with high recovery.

Electrochemical characterization of ascorbic acid oxidation on a graphite screen printed electrode (SPE) modified with La3+/Co3O4nanocubes is performed by applying cyclic voltammetry (CV), chronoamperometry (CHA), and differential pulse voltammetry (DPV) techniques. Synthesized La3+/Co3O4nanocubes for SPE modification, La3+/Co3O4/SPE, enhance the ascorbic acid electrooxidation kinetics by reducing the anodic overpotential. Excellent La3+/Co3O4/SPE electrochemical properties provide sensitive ascorbic acid voltammetric determination with low detection limit, good stability and quick response towards electrooxidation of ascorbic acid as compared to bare SPE. Under optimized conditions, DPV current demonstrates a linear response for ascorbic acid over a concentration range of 1.0 to 900.0 mM with a correlation coefficient of 0.9997, and detection limit (LOD) (S/N = 3) = 0.3 mM. The proposed procedure offers a potential application for producing the sensor with good repeatability. Also, fast response of fabricated sensor can allow a real-time analysis of real samples.

Electrochemical characteristics of carvacrol were investigated on a screen-printed electrode (SPE) modified with La2O3/Co3O4 nanocomposite by using voltammetric techniques, which displayed a well-defined peak for sensitive carvacrol determination in phosphate buffer solution (PBS) at pH 7.0. La2O3/Co3O4 nanoparticles demonstrated suitable catalytic activity for carvacrol determination by differential pulse voltammetry (DPV) technique. Besides, determination of carvacrol in a real samples was recognized in the light of electrochemical findings and a validated voltammetric technique for quantitative analysis of carvacrol in a real formulation was proposed. The DPV peak currents were found to be linear in the concentration range of 10.0 to 800.0 μM. The limit of detection (LOD) was found to be 1.0 μM.

A simple strategy for determination of tryptophan (TRP) based on Fe3O4@SiO2/GO nano­composite modified graphite screen printed electrode (Fe3O4@SiO2/GO/SPE) is re­ported. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were used to characterize the performance of the sensor. The Fe3O4@SiO2/GO/SPE displayed excellent electro­che­mical catalytic activities. The oxidation overpotentials of tryptophan decreased significantly and its oxidation peak current increased dramatically at Fe3O4@SiO2/GO/SPE. Under the optimized experimental conditions tryptophan showed linear response over the range of 1.0-400.0 μM. The lower detection limit was found to be 0.2 μM for tryptophan. The prac­tical application of the modified electrode was demonstrated by measuring the concen­tration of tryptophan in real samples.

The present review focuses on voltammetric and amperometric methods applied for determination of epinephrine (EP) in last five years (2013-2017). Occurrence, role and biological importance of EP, as well as non-electrochemical methods for its assessment, are firstly reviewed. The electrochemical behavior of EP is then illustrated, followed by a description of the voltammetric and amperometric methods for EP content estimation in various media. Different methods for development of electrochemical sensors are reviewed, starting from unmodified electrodes to different composites incorporating carbon nanotubes, ionic liquids or various mediators. From this perspective, the interaction between functional groups of the sensor material and the analyte molecule is discussed, as it is essential for analytical characteristics obtained. The analytical performances of the voltammetric or amperometric chemical and biochemical sensors (linear range of analytical response, sensitivity, precision, stability, response time, etc.) are highlighted. Numerous applications of EP electrochemical sensors in fields like pharmaceutical or clinical analysis where EP represents a key analyte, are also presented.

The notable toxicological impacts of aflatoxin B1 (AFB1) and its main metabolite, aflatoxin M1 (AFM1), on human being health make the evaluation of food quality highly significant. Due to the toxicity of those metabolites—even very low content in foodstuffs—it is crucial to design a sensitive and reliable procedure for their detection. Electrochemical aptamer-based biosensors are considered the most encouraging option, based on multi-placed analysis, rapid response, high sensitivity and specificity. The present review specifically emphasizes the potential utilization of the electrochemical aptasensors for determining the AFM1 and AFB1 with different electrodes.

In recent years, several studies have focused on environmental pollutants. Bisphenol A (BPA) is one prominent industrial raw material, and its extensive utilization and release into the environment constitute an environmental hazard. BPA is considered as to be an endocrine disruptor which mimics hormones, and has a direct relationship to the development and growth of animal and human reproductive systems. Moreover, intensive exposure to the compound is related to prostate and breast cancer, infertility, obesity, and diabetes. Hence, accurate and reliable determination techniques are crucial for preventing human exposure to BPA. Experts in the field have published general electrochemical procedures for detecting BPA. The present timely review critically evaluates diverse chemically modified electrodes using various substances that have been reported in numerous studies in the recent decade for use in electrochemical sensors and biosensors to detect BPA. Additionally, the essential contributions of these substances for the design of electrochemical sensors are presented. It has been predicted that chemically modified electrode-based sensing systems will be possible options for the monitoring of detrimental pollutants.

Venlafaxine (VEN), as one of the popular anti-depressants, is widely utilized for the treatment of major depressive disorder, panic disorder, as well as anxiety. This drug influences the chemicals in the brain, which may result in imbalance in depressed individuals. However, venlafaxine and its metabolites are contaminants in water. They have exerted an adverse influence on living organisms through their migration and transformation in various forms of adsorption, photolysis, hydrolysis, and biodegradation followed by the formation of various active compounds in the environment. Hence, it is crucial to determine VEN with low concentrations in high sensitivity, specificity, and reproducibility. Some analytical techniques have been practically designed to quantify VEN. However, electroanalytical procedures have been of interest due to the superior advantages in comparison to conventional techniques, because such methods feature rapidity, simplicity, sensitivity, and affordability. Therefore, this mini-review aims to present the electrochemical determination of VEN with diverse electrodes, such as carbon paste electrodes, glassy carbon electrodes, mercury-based electrodes, screen-printed electrodes, pencil graphite electrodes, and ion-selective electrodes.