Search Results (119)

Morphine is an opioid extracted from the poppy plant and highly effective for moderate to severe pain management. Development of techniques to measure the concentration of this highly addictive drug in various matrices is very important. This work was aimed at the development of a sensitive electrochemical method for detection of morphine in wastewater. Molecularly imprinted (MIP) electrodes were made by the electro-polymerization process using pyrrole as a monomer. Electro-polymerization was performed on glassy carbon electrodes in the presence of morphine before the extraction of the entrapped morphine molecules. Various techniques were employed to monitor the polymerization and response of the fabricated electrodes toward morphine. These techniques included Fourier transform infrared spectroscopy (FTIR), cyclic voltammetry (CV), square wave voltammetry (SWV), and electrochemical impedance spectroscopy (EIS). The morphine concentration was determined using SWV and CV by measuring the change in the redox peak current of [Fe(CN)₆]^−3/−4. These MIP electrode sensors were used to analyze morphine concentrations between 0 and 80.0 nM solution. The SWV showed a wider linear response region than CV. The detection limit using SWV was found to be 1.9 nM, while using CV, the detection limit was 2.75 nM. This MIP electrode sensor exhibited specificity when other closely related molecules were included and hence has potential as a cheap alternative technique for analysis of morphine. Full article

Recently, it has been found that electrochemical sensing technology is one of the significant approaches for the monitoring of toxic and hazardous substances in food and the environment. Nitrofurazone (NFZ) and nitrofurantoin (NFT) possess a hazardous influence on the environment, aquatic life, and human health. Thus, various advanced materials such as graphene, carbon nanotubes, metal oxides, MXenes, layered double hydroxides (LDHs), polymers, metal–organic frameworks (MOFs), metal-based composites, etc. are widely used for the development of nitrofurazone and nitrofurantoin sensors. This review article summarizes the progress in the fabrication of electrode materials for nitrofurazone and nitrofurantoin sensing applications. The performance of the various electrode materials for nitrofurazone and nitrofurantoin monitoring are discussed. Various electrochemical sensing techniques such as square wave voltammetry (SWV), differential pulse voltammetry (DPV), linear sweep voltammetry (LSV), amperometry (AMP), cyclic voltammetry (CV), and chronoamperometry (CA) are discussed for the determination of NFZ and NFT. It is observed that DPV, SWV, and AMP/CA are more sensitive techniques compared to LSV and CV. The challenges, future perspectives, and limitations of NFZ and NFT sensors are also discussed. It is believed that present article may be useful for electrochemists as well materials scientists who are working to design electrode materials for electrochemical sensing applications. Full article

Presently, extensive research has been conducted on the electrochemical behavior of titanium ions in molten salt, especially in relation to titanium fluoride coordination. However, there is limited research on the coordination between titanium and oxygen. Consequently, this research delved into the influence of oxygen ions on the electrochemical behavior and coordination properties of titanium ions through the utilization of both electrochemical and spectroscopy techniques. The study involved the use of cyclic voltammetry (CV), square wave voltammetry (SWV), and the open-circuit potential (OCP) method to explore the electrochemical properties of titanium ions at different titanium-oxygen ratios. Furthermore, X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy were applied to assess the presence of titanium ions in molten salt and the coordination structure of titanium ions and anions in molten salts, respectively. The results demonstrate that with an increase in oxygen ion content, chloride ions are gradually replaced by oxygen ions, forming TiO_xCl_y^m− complexes. Full article

An electrochemical immunosensor for the quantification of prostate-specific antigens (PSAs) using silver nanocrystals (AgNCs) is reported. The silver nanocrystals were synthesized using a conventional citrate reduction protocol. The silver nanocrystals were characterized using scanning electron microscopy (SEM) and field effect scanning electron microscopy (FESEM), X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), Fourier-transform infrared spectroscopy (FTIR), UV-Vis spectroscopy, and small-angle X-ray scattering (SAXS). The proposed immunosensor was fabricated on a glassy carbon electrode (GCE), sequentially, by drop-coating AgNCs, the electro-deposition of EDC-NHS, the immobilization of anti-PSA antibody (Ab), and dropping of bovine serum albumin (BSA) to prevent non-specific binding sites. Each stage of the fabrication process was characterized by cyclic voltammetry (CV). Using square wave voltammetry (SWV), the proposed immunosensor displayed high sensitivity in detecting PSA over a concentration range of 1 to 10 ng/mL with a detection limit of 1.14 ng/mL and R² of 0.99%. The immunosensor was selective in the presence of interfering substances like glucose, urea, L-cysteine, and alpha-methylacyl-CoA racemase (AMACR) and it showed good stability and repeatability. These results compare favourably with some previously reported results on similar or related technologies for PSA detection. Full article

The aim of the study was to investigate the influence of L-DOPA—the gold standard in the treatment of Parkinson’s disease symptoms—on the electroreduction kinetics of Zn²⁺ ions. It was demonstrated that this effect depends not only on the concentration of the drug but also on the environment in which the process takes place. In the experimental part, cyclic voltammetry (CV), square wave voltammetry (SWV), direct current polarography (DC), and electrochemical impedance spectroscopy (EIS) were used. Based on the obtained results, it was determined that the analyzed electrode reaction, both in the absence and presence of L-DOPA, proceeded in two steps. The kinetic parameters of Zn²⁺ ion electroreduction indicated its quasi-reversible nature in solutions with both pH = 2.0 and pH = 6.0. The presence of the drug in the lower pH solution resulted in a slight slowing down of the electrode process, whereas in the pH = 6.0 solution, it led to a significant acceleration. In both low and high pH solutions, the first step was slower and determined the rate of the entire electrode process. Full article

Organophosphorus pesticides (OPs), while pivotal for agricultural productivity, pose severe environmental and health risks due to their persistence and bioaccumulation. Existing detection methods, such as chromatography and spectroscopy, face limitations in field adaptability, cost, and operational complexity. To address these challenges, this study introduces a novel dual-mode photoelectrochemical–electrochemical (PEC-EC) sensor based on a Co,N-TiO₂@ZrO₂/3DGH nanocomposite. The sensor synergistically integrates zirconium oxide (ZrO₂) for selective OP capture via phosphate-Zr coordination, cobalt-nitrogen co-doped titanium dioxide (Co,N-TiO₂) for visible-light responsiveness, and a three-dimensional graphene hydrogel (3DGH) for enhanced conductivity. In the PEC mode under light irradiation, OP adsorption induces charge recombination, yielding a logarithmic photocurrent attenuation with a detection limit of 0.058 ng mL⁻¹. Subsequently, the EC mode via square wave voltammetry (SWV) self-validates the results, achieving a detection limit of 0.716 ng mL⁻¹. The dual-mode system demonstrates exceptional reproducibility, long-term stability, and selectivity against common interferents. Parallel measurements revealed <5% inter-mode discrepancy, validating the intrinsic self-checking capability. This portable platform bridges the gap between laboratory-grade accuracy and field-deployable simplicity, offering transformative potential for environmental monitoring and food safety management. Full article

Thanks to several components with health-promoting properties, mushrooms are recognized as a practical functional food and a valuable source of nutrients for the food industry. Ergosterol, the major sterol in edible mushrooms and a precursor of vitamin D2 with proven pharmacological activity and nutritional value, has become a very important topic in chemical and medical research. The main objectives of this study were to determine the ergosterol content in different species of Serbian wild mushrooms and in commercial mushrooms from Korean and Serbian grocery stores using square-wave voltammetry, to compare the concentrations in different parts of white button mushrooms, and to determine a possible relationship between Zn, Cu and Fe and ergosterol contents. The ergosterol contents varied between 0.01 and 7.04 mg/g (dry mass) of the mushrooms and were generally higher in cultivated mushrooms than in wild mushrooms. In addition, the ergosterol concentration was higher in the stems than in the caps of the mushrooms examined. Iron, Zn and Cu contents varied between the mushroom species at 8.5–479.9, 13.1–149.7 and 1.62–93.03 mg/kg, respectively, and principal component analysis (PCA) extracted two factors explaining 79.14% of the total variance, suggesting a direct relationship between iron and ergosterol content. This is the first comprehensive study to analyze and evaluate ergosterol concentrations in edible mushrooms from Korea and Serbia. Full article

Designing a highly sensitive and efficient functionalized electrode for precise drug analysis remains a significant challenge. In this work, an electrochemical sensor based on a glassy carbon electrode (GCE) modified with phenyl diazonium salts (ph) and electrochemically reduced graphene oxide (ERGO), labeled GCE/ph/ERGO, was developed for the detection of paracetamol (PAR) in pharmaceutical matrices using square wave voltammetry (SWV). The modified electrode was characterized by scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV). Compared to the bare GCE, the GCE/ph/ERGO sensor demonstrated significantly improved conductivity and anodic current peak for PAR over two orders of magnitude higher, indicating a substantial enhancement in electrochemical performance. Under optimized conditions, the developed sensor exhibited a low detection limit of 18.2 nM and a quantification limit of 60.6 nM. Precision studies yielded relative standard deviations (RSDs) below 8%. The sensor demonstrated excellent selectivity in the presence of common pharmaceutical excipients and high accuracy in the analysis of generic pharmaceutical formulations, with results comparable to those obtained by the HPLC technique. These findings confirm the sensor’s reliability, stability, robustness, and suitability for routine analysis of PAR in pharmaceutical samples. Full article

This paper presents a low-cost wireless prototype designed for point-of-care DNA sensing based on square wave voltammetry (SWV) measurements. Unlike other designs found in the literature, this prototype employs dedicated ADC and DAC components to reduce noise and allows for lower voltage steps in SWV scans. On-board signal processing makes the device suitable for use by inexperienced end-users. The prototype transmits data via Bluetooth Low-Energy (BLE) to a mobile app, which records the measurements on a cloud platform. The prototype was employed to detect a 23-base single-stranded DNA (ssDNA) sequence, within the range of 1 nM to 10 nM. The results obtained with the prototype showed good agreement when compared to a commercial electrochemical analyzer. This study demonstrates the feasibility of using such a device for DNA sensing, highlighting its potential for broader biosensing applications. Full article

This study presents the synthesis, electrochemical characterization, and sensor application of Na₃[Fe(CN)₅(PZT)], a novel pentacyanidoferrate-based coordination compound incorporating 2-pyrazinylethanethiol (PZT) as a ligand. Unlike conventional Prussian blue analogues, this system exhibits enhanced electrocatalytic properties due to its unique ligand framework, which contributes to increased charge transfer efficiency and stability. The complex was synthesized via a controlled ligand substitution reaction, followed by UV-Vis and IR spectroscopy confirmation of its successful formation. The electrochemical properties of the Na₃[Fe(CN)₅(PZT)] complex were investigated using cyclic voltammetry (CV), differential pulse voltammetry (DPV), square-wave voltammetry (SWV), and electrochemical impedance spectroscopy (EIS). Notably, the modified electrodes exhibited improved charge transfer kinetics and catalytic activity, making them promising candidates for electrochemical sensing applications. The Na₃[Fe(CN)₅(PZT)]-modified electrode demonstrated outstanding electrocatalytic performance towards hydrazine oxidation, exhibiting a low detection limit of 7.38 × 10⁻⁶ M, a wide linear response range from 5 to 64 µmol L⁻¹, and high sensitivity. The proposed system enables precise quantification of hydrazine with high selectivity, positioning Na₃[Fe(CN)₅(PZT)] as an effective electrochemical mediator for advanced sensing platforms. These findings provide new insights into the design of next-generation Prussian blue analogue-based sensors with superior analytical performance. Full article

Quantifying progesterone levels in the body is an important indicator of early pregnancy and health. Molecular shape-preserving electrodes have garnered attention in electrochemical biosensors because they can detect targets without the need for expensive enzymes or antibodies. However, some of the currently used methods typically have low electrode durability. Here, progesterone, for which antibodies are typically expensive, was used to develop a molecular shape-preserving electrode using Au to enhance its long-term stability. The physical properties of the electrodes were characterized using scanning electron microscopy (SEM), the electrochemical surface area (ECSA), and cyclic voltammetry (CV). The specific structure of the electrode demonstrated an electrochemical double layer comparable to that of a smooth Au electrode, confirming its high durability. The detection performance was assessed using CV, square wave voltammetry (SWV), and electrochemical impedance spectroscopy (EIS). The current response to progesterone increased in a concentration-dependent manner, but decreased from the saturated state owing to electrodeposition on the surface. Additionally, electrochemical impedance measurements showed high selectivity compared with hormones with similar structures. The fabricated molecular shape-preserving electrode exhibits an excellent durability, stability, and detection performance, confirming its suitability for long-term use. These findings pave the way to new possibilities for electrode fabrication. Full article

This study presents the development of a novel electrochemical sensor for the sensitive and selective detection of triclosan (TSC) on a carbon paste electrode (CPE) modified with graphitic carbon nitride (GCN) and doped with yttrium oxide nanoparticles (Y₂O₃). The materials and proposed electrode were characterized using transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV). The modified sensor exhibited significantly enhanced electrocatalytic activity towards TSC compared to the unmodified CPE. The sensor demonstrated a wide linear detection range, which was obtained using square wave voltammetric method (SWV), with a low limit of detection (LOD) of 0.137 µM and a low limit of quantification (LOQ) of 0.455 µM. The sensor also exhibited excellent selectivity towards TSC in the presence of various interfering substances. The practical applicability of the sensor was evaluated through real-sample analysis, where it was successfully used to determine TSC levels in tap water and toothpaste samples. The sensor demonstrated high recovery rates and minimal matrix effects, indicating its suitability for real-world applications. In conclusion, the developed CPE/Y₂O₃@GCN sensor offers a promising approach for the sensitive, selective, and reliable detection of triclosan in environmental and consumer products. Full article

Bisphenol A (BPA) is a commonly synthetic chemical mainly used in producing plastic items. It is an endocrine-disrupting compound that causes irreversible health and environmental damage. Developing a simple method for BPA effective quantitative monitoring is emergently necessary. Herein, a novel electrochemical sensor for BPA detection based on [(5,10,15,20-tetrakis(p-bromophenyl) porphyrinato] cadmium (II) [(CdTBrPP)] and gold nanoparticle (AuNPs)-modified screen-printed carbon electrode (SPCE) was elaborated. CdTBrPP was synthesized and then characterized with Ultraviolet–Visible Spectroscopy (UV/vis), Infrared Spectroscopy (IR), and Proton Nuclear Magnetic Resonance Spectroscopy (¹H NMR) to confirm its successful synthesis. After drop-coating AuNPs and CdTBrPP on the SPCE, the sensor performance was evaluated using square wave voltammetry (SWV), a linear response in a concentration range from 10⁻¹¹ M to 10⁻² M, with a low detection limit (LOD) of 9.5 pM. The CdTBrPP/AuNPs/SPCE sensor demonstrates a high selectivity and reproducibility, making it a promising candidate for developing a low-cost water-monitoring system for detecting BPA. Additionally, the proposed sensor effectively detected BPA in both tap and mineral water samples. Full article

The metallocenyl-containing β-diketonato rhodium(I) dicarbonyl complexes of [Rh(FcCOCHCOR)(CO)₂] where R = CF₃, 10; Fc = ferrocenyl = Fe^II(C₅H₅)(C₅H₄), 11; Rc = ruthenocenyl = Ru^II(C₅H₅)(C₅H₄), 12; and Oc = osmocenyl = Os^II(C₅H₅)(C₅H₄), 13 were synthesized. Complexes 10–13 were then subjected to an electrochemical study utilizing cyclic voltammetry (CV), square wave voltammetry (SWV), and linear sweep voltammetry (LSV) in the non-coordinating solvent/supporting electrolyte medium CH₂Cl₂/0.1 mol dm⁻³ [N(ⁿBu)₄][B(C₆F₅)₄]. The formal reduction potential for the electrochemical reversible Fc^0/+ couples in 10–13 was identified in the range 0.156 ≤ E^o′ ≤ 0.328 V while the electrochemically irreversible osmocenyl and ruthenocenyl oxidations were observed at peak anodic potentials of E_pa = 0.640 V and E_pa = 0.751 V, respectively. Resolution between the closely overlapping CV-determined Fc^0/+ and Rh^I/II couples was too poor for unambiguous measurement of the Rh^I/II redox potential, but square wave voltammetry allowed estimates of E^o′ (Rh^I/II) in the range 0.156 ≤ E^o′ ≤ 0.398 V. FT-IR spectroelectrochemistry confirmed the one-electron oxidation of Rh^I by the appearance of CO vibrational bands at stretching frequencies, which are associated with rhodium(II) and not rhodium(III). Cytotoxicity tests on 10 (IC₅₀ = 19.2 µM) showed it to be substantially less cytotoxic than the free β-diketone, FcCOCH₂COCF₃, and [Rh(FcCOCHCOCF₃)(cod)]. Full article

In this work, CeBTC (a cerium(III) 1,3,5-benzene-tricarboxylate), was used as a precursor for obtaining CeO₂ nanoparticles (nanoceria) with better sensor performances than CeO₂ nanoparticles synthesized by the solvothermal method. Metal–organic framework-derived nanoceria (MOFdNC) were functionalized with spheric gold nanoparticles (AuNPs) to further improve non-enzymatic electrode material for highly sensitive detection of prominent biocompound uric acid (UA) at this modified carbon paste electrode (MOFdNC/AuNPs&CPE). X-ray powder diffraction (XRPD) and transmission electron microscopy (TEM) analysis were used for morphological structure characterization of the obtained nanostructures. Cyclic voltammetry and electrochemical impedance spectroscopy, both in an [Fe(CN)₆]^3−/4− redox system and uric acid standard solutions, were used for the characterization of material electrocatalytic performances, the selection of optimal electrode modifier, and the estimation of nature and kinetic parameters of the electrode process. Square-wave voltammetry (SWV) was chosen, and the optimal parameters of technique and experimental conditions were established for determining uric acid over MOFdNC/AuNPs&CPE. Together with the development of the sensor, the detection procedure was optimized with the following analytical parameters: linear operating ranges of 0.05 to 1 µM and 1 to 50 µM and a detection limit of 0.011 µM, with outstanding repeatability, reproducibility, and stability of the sensor surface. Anti-interference experiments yielded a stable and nearly unchanged current response with negligible or no change in peak potential. After minor sample pretreatment, the proposed electrode was successfully applied for the quantification of UA in milk. Full article