Search Results (123)

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

This study investigates the development and sensing profile of synthetic melanin nanoparticle-coated electrodes for the electrochemical detection of heavy metals, including lead (Pb), cadmium (Cd), cobalt (Co), zinc (Zn), nickel (Ni), and iron (Fe). Synthetic melanin films were prepared in situ by the deacetylation of diacetoxy indole (DAI) to dihydroxy indole (DHI), followed by the deposition of DHI monomers onto indium tin oxide (ITO) and glassy carbon electrodes (GCE) using cyclic voltammetry (CV), forming a thin layer of synthetic melanin film. The deposition process was characterized by electrochemical quartz crystal microbalance (EQCM) in combination with linear sweep voltammetry (LSV) and amperometry to determine the mass and thickness of the deposited film. Surface morphology and elemental composition were examined using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). In contrast, Fourier-transform infrared (FTIR) and UV–Vis spectroscopy confirmed the melanin’s chemical structure and its polyphenolic functional groups. Differential pulse voltammetry (DPV) and amperometry were employed to evaluate the melanin films’ electrochemical activity and sensitivity for detecting heavy metal ions. Reproducibility and repeatability were rigorously assessed, showing consistent electrochemical performance across multiple electrodes and trials. A comparative analysis of ITO, GCE, and graphite electrodes was conducted to identify the most suitable substrate for melanin film preparation, focusing on stability, electrochemical response, and metal ion sensing efficiency. Finally, the applicability of melanin-coated electrodes was tested on in-house heavy metal water samples, exploring their potential for practical environmental monitoring of toxic heavy metals. The findings highlight synthetic melanin-coated electrodes as a promising platform for sensitive and reliable detection of iron with a sensitivity of 106 nA/ppm and a limit of quantification as low as 1 ppm. Full article

This study presents a comparative analysis of gold nanoparticles electrodeposited on different two-dimensional materials used as electrode substrates, graphene (Gr) and MoS₂, or co-deposited with the metallic material MoS₂. The morphological and electrochemical data demonstrate the efficiency of the electrodeposition process and the preferability of gold nanoparticles for certain attachment sites depending on the nature of the material used as a substrate and the deposition method used. The electrocatalytic activity of the gold nanoparticles obtained in these configurations was evaluated via the oxidation of nitrite ions (NO₂⁻), using both qualitative and quantitative approaches, by cyclic voltammetry and amperometry techniques. The electrocatalytic activity of gold nanoparticles co-deposited with MoS₂ is superior compared to that of gold nanoparticles deposited either on bare gold electrodes or on 2D materials (graphene and MoS₂), showing good performance with a specific sensitivity of 1.043 μA µM⁻¹ cm⁻² on the linear range of 0.5–600 µM nitrite, with a limit of detection of 0.16 µM and good anti-interference ability. Full article

This work presents the development of a biosensing platform for hydrogen peroxide (H₂O₂) electrochemical reduction. The developed platform uses a multi-walled carbon nanotube paste (PMWCNT) and the enzyme cholesterol oxidase (ChOx). The supramolecular architecture of the PMWCNT/ChOx platform was characterized using cyclic voltammetry, electrochemical impedance spectroscopy, and amperometry. The results indicated that the presence of ChOx enhances the sensitivity of electrochemical detection for H₂O₂ by 21 times compared to that without ChOx. The designed electrochemical sensing bio-platform for H₂O₂ shows a sensitivity of 26.15 µA/mM in the linear range from 0.4 to 4.0 mM, an LOD of 0.43 µM, and an LOQ of 1.31 µM. Furthermore, in silico studies (molecular dynamics simulations, molecular docking assays, and binding free energy calculations (ΔG_b)) were carried out to characterize and validate the molecular interaction between ChOx and H₂O₂. The computed data confirmed that the binding is spontaneous, and the type of labile interaction promotes a rapid electrochemical reduction of H₂O₂. Full article

This study investigated the effect of surface treatments on the electrochemical performance of 3D-printed electrodes for versatile applications. The conductive filament was obtained from a mixture of polylactic acid (PLA) and carbon black (CB) at a 7:3 ratio (PLA/CB) dispersed in acetic acid and dichloroethane (3:1) medium. The treatments used were HNO₃, NaOH, DMF (immersion for 30, 30, and 15 min, respectively), and electrochemical activation (amperometry 150 s, 1.8 V). In general, the treatments allow greater exposure of the conductive material and active sites present on the sensor surface. This was confirmed using cyclic voltammetry and electrochemical impedance spectroscopy. The analyses were conducted with a 0.10 M KCl solution containing the redox pair ferricyanide/ferrocyanide 5.00 mmol L⁻¹. Based on the results obtained, the electroactive area, kinetic constant and resistance to electron transfer were determined for each treatment. The treatment in basic medium stood out as the treatment that was most appropriate for the device used in this work. The device was also tested for its potential in the analysis of acetaminophen, demonstrating satisfactory results permitting the application of 3D-S_Basic in the analysis of acetaminophen. Full article

Efforts to quantify iron ion concentrations across fields such as environmental, chemical, health, and food sciences have intensified over the past decade, which drives advancements in analytical methods, particularly electrochemical sensors known for their simplicity, portability, and reliability. The development of electrochemical methods using non-mercury electrodes is increasing as alternatives to environmentally unsafe mercury-based electrodes. However, detecting iron species such as Fe(II) and Fe(III) remains challenging due to their distinct chemical properties, continuous oxidation-state interconversion, presence of interfering species, and complex behavior in diverse environments and matrixes. Selective trace detection demands careful optimization of electrochemical methods, including proper electrode materials selection, electrode surface modifications, operating conditions, and sample pretreatments. This review critically evaluates advancements over the past decade in mercury-free electrode materials and surface modification strategies for iron detection. Strategies include incorporating a variety of nanomaterials, composites, conducting polymers, membranes, and iron-selective ligands to improve sensitivity, selectivity, and performance. Despite advancements, achieving ultra-low detection limits in real-world samples with minimal interference remains challenging and emphasizes the need for enhanced sample pretreatment. This review identifies challenges, knowledge gaps, and future directions and paves the way for advanced iron electrochemical sensors for environmental monitoring, health diagnostics, and analytical precision. Full article

In this work, the influence of surface functionalization due to synthesis conditions of graphene oxide quantum dots GOQDs was evaluated for dopamine (DA) detection. GOQDs were synthesized using HNO₃ (6 M or 8 M) through a liquid-phase oxidation method. The characterization (HRTEM, FTIR, Raman, and XRD) and evaluation by amperometry (AMP) and differential pulse voltammetry (DPV) showed that GOQDs-8 synthesized with higher oxygen content were more sensitive and selective in DA detection than GOQDs-6. The synergistic effects of electrostatic attraction from glassy carbon electrode negatively charged surface, functionalization for inner-sphere mechanism, and edge effect from lower particle size resulted in amplified electrochemical signal achieving detection at nanomolar level using AMP and DPV. When evaluated using AMP, GCE/GOQDs-8 showed a sensitivity of 0.0422 μA μM^–1, a limit of detection (LOD) of 17.6 nM, a linear range from 0.1 to 100 μM, and minimal interference for uric acid, levodopa, and acetaminophen. In contrast, using DPV, the GCE/GOQDs-8 exhibited a sensitivity of 0.0616 μA μM^–1, a LOD of 506 nM, and a linear range from 0.1–30 μM with remarkable selectivity from all interferent species. The assay of GOQDs-8/GCE sensor in normal human serum proved to be feasible for the practical determination of DA. The recovery obtained was in the range of 94.1 to 112.8% with a relative standard deviation (RSD), n = 3 of less than 3.62%. The oxygen-rich material showed a promising performance that can be further improved with additional nanocarbon or conducting polymers supports. Full article

Non-enzymatic glucose detection is an effective strategy to control the blood glucose level of diabetic patients. A novel hierarchical core–shell structure of nickel hydroxide shell coated copper hydroxide core based on copper foam (Ni(OH)₂@Cu(OH)₂-CF) was fabricated and derived from NiO@Cu₂O-CF for glucose sensing. Cyclic voltammetry and amperometry experiments have demonstrated the efficient electrochemical catalysis of glucose under alkaline conditions. The measurement displays that the fabricated sensor exhibits a detection scale of 0.005–4.5 mM with a detection sensitivity of 4.67 µA/µM/cm². It has remarkable response/recovery times in respect of 750 μM glucose (1.0 s/3.5 s). Moreover, the NiO@Cu₂O-CF shows significant selectivity, reliable reproducibility and long-term stability for glucose determination, suggesting it is a suitable candidate for further applications. Full article

Lithium niobate perovskite and silver nanoparticle-based nanocomposites (LNB:AgNPs) were explored for developing an electrochemical glucose sensor. The perovskite to silver nanoparticle ratios investigated were 4:1, 1:1, 1:2, 2:1, and 1:4. Among these, the 4:1 ratio, with the lowest silver content, demonstrated the most stable performance during glucose quantification via amperometry. The sensor’s response was evaluated measuring the current at a fixed potential of 0.7 V following the injection of 1 mM glucose with each addition. The calibration curve obtained from the recorded data exhibited a linear response within the 1 to 15 mM glucose concentration range, achieving a sensitivity of 2 μA/mM, a high correlation coefficient (R² = 0.997), and a limit of detection (LOD) of 0.5 µM. The LNB4:1AgNP composite allowed taking advantage of the unique properties of both components in a balanced manner, maximizing the sensor performance in practical applications. Full article

A novel sandwich-type electrochemical aptasensor based on supramolecularly immobilized affinity bioreceptor was prepared via host–guest interactions. This method utilizes an adamantane-modified, target-responsive hairpin DNA aptamer as a capture molecular receptor, along with a perthiolated β-cyclodextrin (CD) covalently attached to a gold-modified electrode surface as the transduction element. The proposed sensing strategy employed an enzyme-modified aptamer as the signalling element to develop a sandwich-type aptasensor for detecting prostate-specific antigen (PSA). To achieve this, screen-printed carbon electrodes (SPCEs) with electrodeposited reduced graphene oxide (RGO) and gold nanoferns (AuNFs) were modified with the CD derivative to subsequently anchor the adamantane-modified anti-PSA aptamer via supramolecular associations. The sensing mechanism involves the affinity recognition of PSA molecules on the aptamer-enriched electrode surface, followed by the binding of an anti-PSA aptamer–horseradish peroxidase complex as a labelling element. This sandwich-type arrangement produces an analytical signal upon the addition of H₂O₂ and hydroquinone as enzyme substrates. The aptasensor successfully detected the biomarker within a concentration range of 0.5 ng/mL to 50 ng/mL, exhibiting high selectivity and a detection limit of 0.11 ng/mL in PBS. Full article

Abstract: The urine albumin (Alb)-to-creatinine (Crn) ratio (UACR) is a sensitive and early indicator of chronic kidney disease (CKD) and cardiorenal syndrome. This study developed a portable and wireless electrochemical-sensing platform for the sensitive and accurate determination of UACR. The developed platform consists of a carbon nanotube (CNT)-2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid)(ABTS)-based modified UACR sensor, a miniaturised potentiostat, a cup holder embedded with a magnetic stirrer and a smartphone app. The UACR sensing electrode is composed of two screen-printed carbon working electrodes, one screen-printed carbon counter electrode and a screen-printed AgCl reference electrode. The miniaturised potentiostat, which is controlled by the developed app, performs cyclic voltammetry and amperometry to detect Alb and Crn, respectively. Clinical trials of the proposed system by using spot urine samples from 30 diabetic patients indicate that it can accurately classify all three CKD risk statuses within 30 min. The high accuracy of our proposed sensing system exhibits satisfactory agreement with the commercial biochemical analyser TBA-25FR (Y = 0.999X, R² = 0.995). The proposed UACR sensing system offers a convenient, reliable and affordable solution for personal mobile health monitoring and point-of-care urinalysis. Full article

A biocompatible, highly sensitive, and enzyme-free glucose electrochemical sensor was developed based on a copper-cysteamine (Cu-Cy)-modified electrode. The catalytically active biocompatible material Cu-Cy was immobilized on the electrode surface by the natural polymer chitosan (CTS). The electrochemical characterization and glucose response of the Cu-Cy/CTS/glassy carbon electrode (GCE) were investigated by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and constant potential amperometry. The significant electrocatalytic activity of Cu-Cy to the oxidation of glucose in an alkaline environment was revealed. Several crucial parameters, including the number of scanning cycles for electrode activation, applied potential, and the contents of Cu-Cy and chitosan, were investigated to understand their impact on the sensor’s response. The proposed sensing platform exhibited linear ranges of 2.7 μM to 1.3 mM and 1.3 mM to 7.7 mM for glucose detection, coupled with high sensitivity (588.28 and 124.42 μA·mM⁻¹·cm⁻²), and commendable selectivity and stability. Moreover, a Cu-Cy/CTS-modified screen-printed electrode (SPE) was further developed for portable direct detection of glucose in real samples. Full article

Bisphenol A (BPA) has been classified as an endocrine-disrupting substance that may cause adverse effects on human health and the environment. The development of simple and sensitive electrochemical biosensors is crucial for the rapid and effective quantitative determination of BPA. This work presents a study on electrochemical sensors utilizing gold nanoparticle-modified multi-walled carbon nanotubes (CNT/AuNPs). Glassy carbon electrodes (GCEs) and screen-printed electrodes (SPEs) were conveniently modified and used for BPA detection. AuNPs were electrodeposited onto the CNT-modified electrodes using the galvanostatic method. The electrodes were properly modified and characterized by using Raman spectroscopy, cyclic voltammetry (CV), and electrochemical impedance analysis (EIS). The electrochemical response of the sensors was studied using differential pulse voltammetry (DPV) and constant potential amperometry (CPA) for modified GCE and SPE electrodes, respectively, and the main analytical parameters were studied and optimized. Problems encountered with the use of GCEs, such as sensor degradation and high limit of detection (LOD), were overcome by using modified SPEs and a flow injection device for the measurements. Under this approach, an LOD as low as 5 nM (S/N = 3) was achieved and presented a linear range up to 20 μM. Finally, our investigation addressed interference, reproducibility, and reusability aspects, successfully identifying BPA in both spiked and authentic samples, including commercial and tap waters. These findings underscore the practical applicability of our method for accurate BPA detection in real-world scenarios. Notably, the integration of SPEs and a flow injection device facilitated simplified automation, offering an exceptionally efficient and reliable solution for precise BPA detection in water analysis laboratories. Full article

L-Lactate is an important bioanalyte in the food industry, biotechnology, and human healthcare. In this work, we report the development of a new L-lactate electrochemical biosensor based on the use of multiwalled carbon nanotubes non-covalently functionalized with avidin (MWCNT-Av) deposited at glassy carbon electrodes (GCEs) as anchoring sites for the bioaffinity-based immobilization of a new recombinant biotinylated lactate oxidase (bLOx) produced in Escherichia coli through in vivo biotinylation. The specific binding of MWCNT-Av to bLOx was characterized by amperometry, surface plasmon resonance (SPR), and electrochemical impedance spectroscopy (EIS). The amperometric detection of L-lactate was performed at −0.100 V, with a linear range between 100 and 700 µM, a detection limit of 33 µM, and a quantification limit of 100 µM. The proposed biosensor (GCE/MWCNT-Av/bLOx) showed a reproducibility of 6.0% and it was successfully used for determining L-lactate in food and enriched serum samples. Full article

A new, simple, and effective one-step reduction method was applied to prepare a nanocomposite with spherical polycrystalline silver nanoparticles attached to the surface of reduced graphene oxide (Ag@rGO) at room temperature. Equipment such as X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FTIR) was used to characterize the morphology and composition of the Ag@rGO nanocomposite. A novel electrochemical sensor for detecting L-cysteine was proposed based on fixing Ag@rGO onto a glassy carbon electrode. The electrocatalytic behavior of the sensor was studied via cyclic voltammetry and amperometry. The results indicate that due to the synergistic effect of graphene with a large surface area, abundant active sites, and silver nanoparticles with good conductivity and high catalytic activity, Ag@rGO nanocomposites exhibit significant electrocatalytic activity toward L-cysteine. Under optimal conditions, the constructed Ag@rGO electrochemical sensor has a wide detection range of 0.1–470 μM for L-cysteine, low detection limit of 0.057 μM, and high sensitivity of 215.36 nA M⁻¹ cm⁻². In addition, the modified electrode exhibits good anti-interference, reproducibility, and stability. Full article