Modified Carbon Paste Electrode Research Articles

A Microsphere Dual‐Ligand MOFs Modified Carbon Paste Electrode and Its Application as Electrochemical Sensor for Bisphenol A and Metal Ions

ABSTRACTThis study introduces a new electrochemical sensor for bisphenol A (BPA) and metal ions utilizing a microsphere dual‐ligand Ni‐based MOFs modified carbon paste. The MOFs (Ni‐bipy‐btc) synthesized from dual‐ligands were prepared via a hydrothermal method and characterized using X‐ray diffraction (XRD), scanning electron microscope (SEM), FT‐IR spectrometer, X‐ray photoelectron spectrum (XPS), and specific surface area test (BET) analysis. The resulting MOFs exhibited promising performance as electrode materials for electrochemical sensors targeting the detection of BPA and heavy metal ions (Pb2+ and Cu2+). The linear range of the MOFs (Ni‐bipy‐btc)/CPE electrode for BPA detection ranged from 0.2 to 150 μM, with a detection limit of 0.045 μM, demonstrating robust immunity and stability. Additionally, the limit of detection for the MOFs (Ni‐bipy‐btc)/CPE electrode was found to be 4.3 and 9.5 nM for Pb2+ and Cu2+ ions, respectively, showcasing excellent stability and reproducibility. This study presents a straightforward approach for the highly sensitive electrochemical detection of BPA and heavy metal ions using a simple hydrothermal reaction method.

Multifunctional applications of novel copper magnesium vanadate nanoparticles: Photocatalytic dye degradation and electrochemical properties

The multifunctional applications of nanomaterials in energy saving, electrochemical energy storage, and sensing devices are a current research trend. Novel Copper Magnesium Vanadate (CMV-CuMg2V2O8) nanoparticles have been synthesized by solution combustion method. The crystallite size calculated from XRD and TEM results was found to be 21 nm. The band gap estimated from UV–Vis DRS of CMV nanoparticles was found to be 3.82 eV. Its multifunctional applications were explored through for energy conversion, storage and sensing applications. Photocatalytic degradation of Acid Red-88 (AR-88) dye was conducted using CMV nanoparticles as photocatalyst under UV light. CMV nanoparticles modified carbon paste electrodes were prepared and its cyclic voltammetry (CV), Electrochemical impedence spectroscopy (EIS) and Galvanostatic charge–discharge (GCD) analysis were carried out using 1M KCl and NaOH electrolyte. With excellent specific capacitance of 266 Fg−1 in KCl electrolyte and 242 Fg−1 in NaOH electrolyte at 5 mV/s scan rate, CMV NPs was demonstrated to be a promising electrode material for supercapacitors. Electrochemical sensing analysis was carried out using the same electrode for the detection of paracetamol and ibuprofen within the range of 1–5 mM. The resulting copper magnesium vanadate nanoparticles have been verified as a possible electrode material for next-generation energy storage devices.

Electrochemical Determination of Dopamine with a Carbon Paste-Lanthanum (III) Oxide Micro-Composite Electrode: Effect of Cetyl Trimethyl Ammonium Bromide Surfactanton Selectivity.

This paper presents a new application of a lanthanum oxide (III)-modified carbon paste electrode (LaOX/CPE) for dopamine (DP) detection in the presence of ascorbic acid (AA). The presence of cetyl trimethyl ammonium bromide (CTAB) facilitated the LaOX/CPE electrode's ability to detect DP amidst AA interference, resulting in a substantial 70.0% increase in the anodic peak current for DP when compared to the unmodified carbon paste electrode (CPE). CTAB enabled clear separation of the anodic peaks for DP and AA by nearly 0.2 V, despite their initially overlapping potential values, through the ion-dipole interaction of AA and CTAB. The electrode was characterized using cyclic voltammetry (CV) and energy-dispersive spectroscopy (EDS). The method demonstrated a detection limit of 0.06 µmol/L with a relative standard deviation (RSD) of 6.0% (n = 15). Accuracy was assessed through the relative error and recovery percent, using urine samples spiked with known quantities of DP.

Sensitive electrochemical analysis of uricosuric drug sulfinpyrazone using a graphene-based sensor: A first voltammetric approach

The novel electrochemical sensor was employed for the investigation of the uricosuric drug sulfinpyrazone (SLF), which is administered orally to treat gout and prevent stone formations. SLF is toxic to the liver and increases the risk of Stevens-Johnson syndrome and toxic epidermal necrolysis, which are life-threatening conditions. It is crucial to avoid aspirin, salicylates, and similar salicylic acid derivatives when taking uricosuric drugs, as salicylates can inhibit tubular uric acid secretion, especially at lower doses. Thus, determining SLF is highly significant. In the pursuit of intensive care and interactions involving SLF, an r-GO@CPE (reduced graphene oxide modified carbon paste electrode) was employed for the study of SLF. Various characterization techniques, such as X-ray diffraction (XRD), scanning electron microscopy (SEM) with energy dispersive X-ray diffraction spectrum (EDS), Fourier Transform Infrared Spectroscopy (FTIR) and electron impedance spectroscopy (EIS), were utilized to analyse the electrode modifier. The resulting r-GO@CPE has an enriched electroactive surface area, a high standard heterogeneous rate constant (ket), and a small charge resistance (Rct) as compared with the Carbon paste electrode, which authenticates its good catalytic activity. The analytical investigation of SLF was achieved through voltametric techniques such as cyclic & square wave voltammetry (CV & SWV). Optimal results were attained at a pH of 9.2, revealing an oxidation peak within the potential range of 0.2–1.2 V. SWV was employed for the quantitative estimation of SLF, yielding a limit of detection (LOD) and a limit of quantification (LOQ) of 1.10 × 10−8 M and 3.6 × 10−8 M respectively. This novel approach was also applied to determine SLF concentrations in both biological, water & pharmaceutical samples.

Nickel-doped tungsten fabricated electrode for electrochemical sensing of amoxicillin

One of the most popular antibiotics used in human medicine is amoxicillin (AML). It is frequently applied to humans and animals to avoid or treat infections caused by bacteria. However, considering its widespread application and excessive use of AML, it could harm the environment and the general world because of the hazardous potential of its pharmaceutical industry effluents. Additionally, some unpleasant compounds might be left behind due to the extensive use of these animals in food production. Hence, AML may be the root cause of several illnesses, including rashes, nausea, vomiting, and colitis linked to antibiotics, if it is present in biological fluids in sufficient quantities. Aquatic habitats where it accumulates can give rise to bacterial species that are susceptible to it. Novel electroanalytical methods with sensitive and quick examination abilities are required to identify and quantify the level of AML in drugs, biological fluids, environmental pollutants, and foods. We have developed a novel sensor that quantitatively detects AML using a modified carbon paste electrode containing nickel-doped tungsten oxide (Ni-WO3). Findings show that Ni-WO3 acts as an electrocatalyst in the oxidation of AML. AML-wide concentration showed a strong linear response from this electrocatalytic oxidation encompassing the range of 0.05 μM to 0.9 μMwith a low detection limit of 8.68 × 10−9 M. As a result, the current electrocatalytic method provides a quick, accurate, and simple method to detect AML in biological medium and pharmaceutical formulations. A sensor with excellent reproducibility, short response times, and outstanding stability has been described as the modified electrode.

Potentiometric determination of nitrazepam in pharmaceutical dosage form and spiked plasma using a novel modified carbon paste electrode

AbstractA newly prepared solid contact ion selective electrode based on polyvinyl chloride membrane has been optimized and developed for determining nitrazepam in its pure form and synthetically prepared tablet dosage form. The proposed electrode was fabricated based on zeolite modified carbon paste electrode as a solid contact acting as a support for the membrane of PVC containing the ion complex of nitrazepam‐tetraphenyl borate as an electroactive material, and the plasticizer dibutyl phthalate. By improving the composition, the potentiometric properties were further enhanced, and the sensor achieved a Nernstian slope of 60.89 mV dec−1. The sensor was effective for detecting nitrazepam in the concentration range of 1.0×10−7 to 1.0×10−2 M, with a detection limit of 4.7×10−8 M. The sensor demonstrated excellent reversibility and reproducibility with a fast response time and application over a wide pH range. The developed electrode showed no significant effect when tested with various interfering species. It is successfully applied for accurate determination of nitrazepam in pure form, synthetically prepared tablet and spiked human plasma. The developed technique was validated and demonstrated high accuracy and precision. When compared statistically with the official method, there were no significant differences observed.

Characterization of wine polyphenols with a carbon/nanoparticle TiO2 electrode

The positive effects of polyphenolic compounds on the sensory characteristics of wine and human health indicate a great need for a simple, fast and easily accessible method to determine the content of polyphenols in wine. The aim of this study is the electrochemical characterization of polyphenolic compounds in natural wine samples using a modified carbon paste electrode with TiO2 nanoparticles (MCPE/npTiO2) and improved voltammo­gram processing to obtain indicative data for polyphenols. The most marked influence of the modification of CPE with TiO2 nanoparticles was an increased sensitivity to electrooxi­dation, which is reflected in an increase of the anodic peak current. Of the five tested poly­phenols, i.e., gallic acid (GA), caffeic acid (CA), catechin (CT), quercetin (QV) and resveratrol (RE), the current maximum of the first two oxidation peaks increased only for GA by a factor of about 2 and for CT by a factor of about 1.5. Of the three red wines, Vranac (VR), Merlot (ME), Cabernet Sauvignon (CS); three white wines, Graševina (GR), Temjanika (TE), Char­donnay (CS) and one rose wine, Belrose Mediterranée Rosé (RO) tested, an increase by a factor of about 2.5 was observed for two red wines (VR, CS) and by a factor of 1.5 for one red wine (ME), one white wine (GR), and the rose wine (RO), while no increase in the current signal was observed for one of the white wines (CS). The most significant increase in the voltam­metric signal of GA at the MCPE/npTiO2 compared to other studied polyphenols can be explained by its higher affinity for adsorption on TiO2 nanoparticles. The investigated modified electrode provides an improved, linear and reproducible voltammetric response in wine samples. Consequently, MCPE/npTiO2 represents a good basis for the further deve­lopment of an integrated sensor/data system with the possibility of a broader application for the detection of polyphenols, especially GA, as an aroma and visually relevant parameter in winemaking.

An Efficient Electrochemical Sensing of Hydrogen Peroxide on Zn-Based Coordination Polymer Decorated Carbon Paste Electrode

Due to the important role of hydrogen peroxide (H2O2) in biological systems and its wide range of practical applications, the development of efficient electrochemical H2O2 sensors has become a highly attractive research area. Herein, we reports the synthesis and fabrication of zinc-based coordination polymer [Zn(bim)(L1)(Cl)]n (CP-a): [bim = 1-benzylimidazole, L1 = terephthalic acid] on modified carbon paste electrode (CP-a/CPE) for the electrochemical detection of H2O2. The surface morphology of CP-a/CPE was confirmed by field emission scanning electron microscopy. Electrochemical sensing features were evaluated by cyclic voltammetry and chrono-amperometry. The linear range at the potential of −0.5 V based on CP-a/CPE for H2O2 was 0.001 mM–60 mM, with a low detection limit (LOD) of 0.0004 mM. The effect of interfering species on the reduction peak current response shows a minor change of signals (>5%). The as-synthesized CP-a/CPE sensor exhibited efficient reproducibility and stability. The electrocatalytic activity and good performance imply that the metal-based coordination polymers are potential candidates for fabricating electrochemical sensors.

An electrochemical 3D platform using poly (alizarin red S) and magnetite nanoparticles for rapid recognition and determination of tryptophan enantiomers in whole blood samples

The construction of a simple and convenient electrochemical platform for the recognition of enantiomers is crucial for the life sciences and medical fields. Herein, a portable electrochemical 3D platform based on a carbon paste electrode modified (CPE) with poly (alizarin red S) (PARS) and magnetite nanoparticles (Fe3O4NPs) for the recognition and determination of tryptophan enantiomers from whole blood samples was developed. Several methods, including scanning electron microscopy (SEM), differential pulse voltammetry (DPV), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS), were used to evaluate the morphologies and electrochemical behaviors of the modified electrode. The synthesized magnetite nanoparticles are studied using SEM with energy-dispersive X-ray analysis (EDAX). Under the optimum experimental conditions, the current intensity ratio of d-Trp to l-Trp (ID/IL) was found to be 1.32 at PARS/Fe3O4NPs/CPE, according to the results of differential pulse voltammetry. Furthermore, the developed platform showed a good linear correlation between response current intensity and tryptophan enantiomer concentration, ranging from 0.001 to 0.2 mM. The detection limits for both d-Trp and l-Trp were found to be 0.3 µM. This study demonstrates that the designed platform is capable of rapidly detecting the enantiomeric ratio in a non-racemic tryptophan mixed solution. Finally, the proposed platform was used to identify the Trp enantiomers in human whole blood, confirming the effectiveness of the modified electrode in analyzing real samples. The electrochemical 3D platform is thus used not only to recognize tryptophan enantiomers but also exhibits a significant promise for practical uses.

A simple and efficient electrochemical sensor for folic acid determination on Ti(OH)4 modified carbon paste electrode

Folic acid (FA) has a crucial function in pregnant women and anemic patients. Having adequate FA prior to and during the gestation period can protect the brain of the child and spine from significant birth abnormalities. It reduces the risk of stroke, heart disease and some types of cancers, etc. Thus, FA is employed as a reliable biomarker in the early identification of various disorders. In the present study, we synthesized titanium tetra hydroxide [Ti(OH)4] nanoparticles (NPs) by precipitation method with annealing at 100 °C, which is used to modify carbon paste electrode (Ti(OH)4 /MCPE). FA is detected here by voltammetry method using Ti(OH)4/MCPE in the phosphate buffer of pH 6 and compared with bare and TiO2-400, TiO2-600 and TiO2-800 °C NPs MCPE. Based on ac-impedance spectra, the conductivity of Ti(OH)4/MCPE was found to be higher, and consequently this electrode showed excellent sensitivity of 5.5 µA µM−1 cm−2. Lower detection limit (1.3 nM) was observed in the concentration range of 0.4–30 μM by differential pulse voltammetry. The Ti(OH)4/MCPE was also effective for the determination of FA in real samples such as orange, banana, spinach and tablet. The electrochemical sensor investigated here showed excellent stability (92 %) up to 30 days.

Zirconia nanoparticles/carbon quantum dots modified carbon paste electrode as electrochemical sensor for determination of antiepileptic drug eslicarbazepine acetate in bulk and pharmaceutical dosage form

A new, sensitive and selective electrochemical method has been developed for determination of the antiepileptic prodrug eslicarbazepine acetate (ESL) that is used for the treatment of partial-onset seizures in adults with epilepsy. It belongs to the class of sodium channel blockers called dibenzoazepine family. A novel modified zirconia nanoparticles carbon paste nanocomposite, carbon dots sensor prepared from banana peels by solvothermal method has been fabricated. The voltammetric method is based on the direct anodic oxidation of ESL at the electrode surface using differential pulse voltammetry. Under the optimum experimental conditions, ESL exhibited a linear relationship in the range of 3.04 × 10-8 to 9.66 × 10-5 M with a lower detection limit of 7.57 × 10-9 M and quantification limit of 2.29 × 10-8 M. The proposed method was validated according to ICH guidelines and was applied for estimating ESL in raw material showing high accuracy and precision with successful application on tablet dosage form.

Raw clay material-based modified carbon paste electrodes for sensitive heavy metal detection in drinking water

A new electrode based on carbon paste (CP) modified with natural clay was used for heavy metals detection. The investigation of the raw clay material (X-ray diffraction, infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, thermal analysis and particle size distribution) revealed different morpho-structural properties of the natural material. The electrochemical behaviour of the modified carbon paste electrode and its ability to detect heavy metals (Zn2+, Cd2+, and Cu2+) was studied by different electrochemical techniques like cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and square wave anodic stripping voltammetry (SWASV). Both electrochemical and analytical parameters of the investigated modified electrode recommend them as stable, sensitive and reproducible sensors for individual heavy metals detection.

Electrochemical Determination of Cyclobenzaprine Hydrochloride Muscle Relaxant Using Novel S-GCN/TiO2-Based Carbon Electrode.

We have successfully prepared the titanium dioxide (TiO2) nanoparticles (NPs) and sulfur-incorporated graphitic carbon nitride (S-GCN)-modified carbon paste electrode (CPE). The CPEs modified with TiO2 NPs and S-GCN were employed for detecting and quantifying the skeletal muscle relaxant cyclobenzaprine hydrochloride (CBP) using cyclic voltammetry and square wave voltammetry (SWV) techniques. Optimal electrochemical conditions were indicated by the pH study results, with the highest peak current observed at a physiological pH of 7.4. The electrochemical process was determined to involve an equivalent number of protons (H+) and electrons (e-). The concentration variation of CBP (ranging from 0.06 to 10 × 10-7 mol L-1) was explored using SWV. The limits of detection and quantification were determined as 6.4 × 10-9 and 2.1 × 10-8 M, respectively. The proposed electrode configuration was applied to analyze real samples, including water, biomedical, and pharmaceutical specimens.

Development and characterization of ss-DNA/RGO/MoS2 modified carbon paste electrode for highly sensitive detection of capecitabine

Capecitabine (CAP) is a chemotherapeutic agent used in cancer treatment, necessitating the development of sensitive and selective detection methods for its analysis in clinical samples. The present research utilized a simplified procedure for developing a novel electrochemical sensor based on a carbon paste electrode (CPE) modified with single-stranded DNA (ss-DNA), reduced graphene oxide (RGO), and molybdenum disulfide (MoS2). Unmodified (bare CPE) and modified (ss-DNA/RGO/MoS2/CPE) electrodes were characterized by scanning electron microscopy (SEM), EDX analysis, and cyclic voltammetry (CV). Characterization data confirm the good conductivity and electrocatalytic nature with more electrochemically active sites in ss-DNA/RGO/MoS2/CPE compared to bare CPE in the determination of CAP in real samples. Two linear ranges were obtained for CAP concentration within the ranges of 0.01–10.00 μM and 10.00–60.00 μM, with a detection limit of 0.0108 μM and a limit of quantification of 0.036 μM. The lower linear concentration range of 0.01–10.00 μM showed a sensitivity of 276.85 AM−1 cm−2, while the range of 10–60 μM had a sensitivity of 5.88 AM−1 cm−2. The performance of the modified electrode was tested in human serum samples, yielding satisfactory recovery results. The selectivity and practical ability of ss-DNA/RGO/MoS2/CPE to determine CAP in the presence of different interfering species were investigated, demonstrating the sensor's selective, reliable, and accurate response.

Para-Hydroxy Ni(II)-POCOP Pincer Complexes as Modifiers on Carbon Paste Electrodes and Their Application in Methanol Electro-Oxidation in Alkaline Media

The application of organometallic materials as anodes in fuel cell devices has experienced a notable increase in recent years. However, the use of POCOP pincer complexes remains scarcely explored despite their great relevance in catalysis. Thus, in this work, the electrocatalytic activity to methanol in alkaline media of three Ni(II)-based POCOP pincer complexes—[NiCl{C6H2-4-OH-2,6-(OPiPr2)2}] (a1), [NiCl{C6H2-4-OH-2,6-(OPtBu2)2}] (a2), and [NiCl{C6H2-4-OH-2,6-(OPPh2)2}] (a3)—will be discussed. The complexes were use as modifiers of carbon paste electrodes that were evaluated using cyclic voltammetry considering diverse factors, such as the absence and presence of MeOH, diverse proportions (% w/w) of the complex in the electrode, scan rate, and different MeOH concentrations. Results indicated the presence of a redox pair Ni(II)/Ni(III) with a quasi-reversible behavior in all complexes, the anodic peak currents of which were proportional to the increase in MeOH concentrations (0.05–0.3 mM), and their oxidation potentials varied in the function of the P-substituent in the Ni(II)-POCOPs backbone. Complex a1 exhibited the best current density (429.5 mA cm2 at 0.5 mM) compared to its analogs a2 and a3. The current intensity of all electrodes displays good stability, which remains—with slight changes—up to 100 s. Moreover, a comparison of their catalytic rate constants suggested a great activity in complex a1 (0.52 × 106 cm3 mol−1 s−1) compared to its analogues, implying a great activity in the electro-oxidation of MeOH. Hence, this work opens new opportunities for the electrochemical application of POCOPs complexes for future DMFCs development.

A stable electrochemical sensor for the detection of ascorbic acid based on Fe3O4/ZrO2 nano composite modified carbon paste electrode

A stable electrochemical sensor for the detection of ascorbic acid based on Fe3O4/ZrO2 nano composite modified carbon paste electrode

Electrochemical determination of dopamine by poly (methyl orange) shape memory alloy modified carbon paste electrode

We have successfully prepared 50Ni-30Ti-20Hf shape memory alloy powders using a high-energy planetary ball mill for 20 h by wet milling. The fabricated shape memory alloy powders were characterized by X-ray diffraction (XRD), and scanning electron microscope (SEM) to investigate the phases present and the morphology of the powders respectively. The use of 50Ni-30Ti-20Hf (nitinol) shape memory alloy powders as electro-catalytic materials is a unique and new idea. We are the first researchers to use nitinol powders as dopamine (DA) electrochemical sensors. For better electrochemical oxidation and higher current response of DA, we have electro-polymerized the surface of nitinol-modified carbon paste electrode (MCPE) with methyl orange (MO). Using poly(MO)-NiTiHf-MCPE, we have determined the DA using cyclic voltammetry (CV) and differential pulse voltammetry (DPV) respectively. The calculated active surface area for BCPE, NiTiHf-MCPE, and the poly(MO)-NiTiHf-MCPE were found to be 0.044, 0.089, and 0.098 cm2 respectively. The electro-polymerized nitinol MCPE not only increased the surface area but also increased the electron transfer kinetics. Our results confirmed the participation of 2 electrons and 2 protons in the electrochemical redox reaction.

Electroadsorption of La3+ and Ce3+ from aqueous media with a carbon paste electrode modified with HMS-CMPO

This work deals with the electroadsorption of rare earths cerium and lanthanum in aqueous solution by using a carbon paste electrode modified with a silica mesoporous material functionalized with carbamoyl methyl phosphine oxide (CMPO). This functionalization was carried out in a two-step synthesis, the intermediate product was synthesized by attaching N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (APTMS) to the surface of the HMS by a grafting method synthesis, then this intermediate was modified by CMPO, in a further condensation reaction. The final product CMPO obtained was characterized by diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), thermal gravimetric analysis (TGA) and N2 adsorption/desorption isotherms using BJH and BET models. Showing thermal stability, a surface area higher than 450m2g-1 and mesoporous properties. The CMPO material was used to modify the mixture of the carbon paste electrode producing an enhancement in the interaction between the electrode surface and the lanthanides studied, at the same time it produces and improvement in the electroactive area by over two orders of magnitude. The modified carbon paste electrode (CMPO-CPE) developed in this work shows an increase in the conductivity, observed with the electrochemical impedance spectroscopy studies, and an increase in the electroactive area of 47 % was calculated from cyclic voltammetry experiments. CMPO-CPE was used to extract La3+ and Ce3+ from aqueous solution using NaNO3 as support electrolyte, by using a fixed potential program over time, measuring the obtained current by Chronoamperometric method. The adsorption and desorption results were corroborated with Inductively coupled plasma atomic emission spectroscopy (ICP-OES) demonstrated the capacity of extraction of the electrode were 74 μg after ten cycles for La3+ at pH 5.0 and 15 μg after ten cycles for Ce3+ at pH 6.0, using a CMPO modified electrode of small surface (3 mm radius). This electrode was tested for over 50 cycles without losing their electroactive properties under tested electrochemical conditions.

Electrochemical Detection of Nitrite on PANI-TiO2/Pt Nanocomposite-Modified Carbon Paste Electrodes Using TOPSIS and Taguchi Methods.

Platinum nanoparticles are widely used in electrocatalysis and sensors. In this work, a novel modified carbon paste electrode based on PANI-TiO2/Pt nanocomposites was developed electrochemically. To improve the performance of the PANI-TiO2/Pt composite-modified electrode, a Taguchi orthogonal array was used for experimental design, and the best values of factors affecting the performance were determined using the technique for order preference by similarity to ideal solution (TOPSIS) and Taguchi optimization methods. The electrochemical catalytic activities of the PANI-TiO2/Pt composite-modified electrode on the oxidation of nitrite was calculated by electrochemical analysis. The experimental results demonstrate that the PANI-TiO2/Pt electrode has pretty excellent electrocatalytic ability for the oxidation of nitrite. The sensing performances of the proposed electrode were evaluated, including linear detection range, sensitivity, LOD, selectivity, and stability for nitrite sensing.

Electrochemical sensing platform based on two-dimensional Ni-MOF and ionic liquid modified carbon paste electrode for simultaneous determination of levodopa and cabergoline

Electrochemical sensing platform based on two-dimensional Ni-MOF and ionic liquid modified carbon paste electrode for simultaneous determination of levodopa and cabergoline