Search Results (326)

Unrefined psyllium husk derived from Plantago ovata constitutes a complex mixture of water-soluble and insoluble polymeric chains that form an interpenetrating network capable of entrapping carbon nanoparticles. While the resulting composite was found to swell in aqueous electrolyte, it exhibited hydrogel-like properties where the electrochemical activity was retained and found to be stable upon repetitive voltammetric cycling. Planar film systems were characterized by electron microscopy, Raman spectroscopy, tensile testing, gravimetric analysis, contact angle and cyclic voltammetry. A key advantage of the composite lies in its ability to be cast in 3D geometric forms such as pyramidal microneedle arrays (700 μm high × 200 μm base × 500 μm pitch) that could serve as viable electrode sensors. In contrast to conventional composite electrode materials that rely on non-aqueous solvents, the psyllium mixture is processed entirely from an aqueous solution. This, along with its plant-based origins and simple processing requirements, provides a versatile matrix for the design of biodegradable electrode structures that can be manufactured from more sustainable sources. Full article

Contamination of food with heavy metals is an important factor leading to serious health concerns. Rapid identification of these heavy metals is of utmost priority. There are several methods to identify traces of heavy metals in food. Conventional methods for the detection of heavy metal residues have their limitations in terms of cost, analysis time, and complexity. In the last decade, voltammetric analysis has emerged as the most prominent electrochemical determination method for heavy metals. Voltammetry is a reliable, cost-effective, and rapid determination method. This review provides a detailed primer on recent advances in the development and application of graphene-based electrochemical sensors for heavy metal monitoring over the last decade. We critically examine aspects of graphene modification (fabrication process, stability, cost, reproducibility) and analytical properties (sensitivity, selectivity, rapid detection, lower detection, and matrix effects) of these sensors. Furthermore, to our knowledge, meta-analyses were performed for the first time for all investigated parameters, categorized based on graphene materials and heavy metal types. We also examined the pass–fail criteria according to the WHO drinking water guidelines. In addition, the effects of heavy metal toxicity on human health and the environment are discussed. Finally, the contribution of heavy metal contamination to the seventeen Sustainable Development Goals (SDGs) stated by the United Nations in 2015 is discussed in detail. The results confirm the significant impact of heavy metal contamination across twelve SDGs. This review critically examines the existing knowledge in this field and highlights significant research gaps and future opportunities. It is intended as a resource for researchers working on graphene-based electrochemical sensors for the detection of heavy metals in food safety, with the ultimate goal of improving consumer health protection. Full article

In this study, a boron-doped diamond (BDD) sensor was used to study the electroanalytical behavior of emerging contaminants (ECs), such as caffeine, paracetamol and methyl orange. BDD shows strong resolving power for the superimposed voltammetric response of ECs in well-resolved peaks with increased peak current. Differential pulse voltammetry, which is an electroanalytical technique, was compared with two reference techniques including absorption spectrophotometry in the UV-vis region and high-performance liquid chromatography (HPLC) in the detection and quantification of ECs. The results obtained were satisfactory, as the complete removal of ECs was achieved in all applied processes. The detection limits were 0.69 mg L⁻¹, 0.84 mg L⁻¹ and 0.46 mg L⁻¹ for CAF, PAR and MO, respectively. The comparison of electroanalysis results with those obtained by UV-vis and HPLC established and confirmed the potential applicability of the technique for determining CAF, PAR and MO analytes in synthetic effluents and environmental water samples (tap water, groundwater and lagoon water). The electrochemical approach can therefore be highlighted for its low consumption of reagents, ease of operation, time of analysis and excellent precision and accuracy, because these are characteristics that enable the use of this technique as another means of determining analytes in effluents. Full article

This paper proposes an environmentally friendly sensor for determining trace amounts of diclofenac (DCF)—an activated glassy carbon electrode (aGCE). Such a sensor was achieved by simple surface activation of a glassy carbon electrode to perform five cyclic voltammetric scans from −1.5 to 2.5 V at a scan rate (υ) of 100 mV/s in 0.1 M NaOH. This type of activation results in the formation of surface functional groups, which provide several advantages such as the creation of new active sites, the improvement of electron transfer dynamics, and sensor electrocatalytic activity. The electrode prepared in this way was used to develop a new differential pulse adsorptive stripping voltammetric procedure (DPAdSV) for rapid, simple, and sensitive DCF analysis. Thanks to this procedure, the following calibration curve range was obtained: 1–100 nM with low detection and quantification limits of 0.25 and 0.83 nM, respectively. To show the practical application of the method, DCF was successfully determined in commercially available pharmaceutical preparations with the standard addition method. Full article

Promethazine hydrochloride (PMH) is a first-generation antipsychotic drug created from phenothiazine derivatives that is widely employed to treat psychiatric disorders in human healthcare systems. However, an overdose or long-term intake of PMH can lead to severe health issues in humans. Hence, establishing a sensitive, accurate, and efficient detection approach to detect PMH in human samples is imperative. In this study, we designed orthorhombic copper molybdate microspheres decorated on reduced graphene oxide (Cu₃Mo₂O₉/RGO) composite via the effective one-pot hydrothermal method. The structural and morphological features of the designed hybrid were studied using various spectroscopic methods. Subsequently, the electrochemical activity of the composite-modified screen-printed carbon electrode (Cu₃Mo₂O₉/RGO/SPCE) was assessed by employing voltammetric methods for PMH sensing. Owing to the uniform composition and structural benefits, the combination of Cu₃Mo₂O₉ and RGO has not only improved electrochemical properties but also enhanced the electron transport between PMH and Cu₃Mo₂O₉/RGO. As a result, the Cu₃Mo₂O₉/RGO/SPCE exhibited a broad linear range of 0.4–420.8 µM with a low limit of detection (LoD) of 0.015 µM, highlighting excellent electrocatalytic performance to PMH. It also demonstrated good cyclic stability, reproducibility, and selectivity in the presence of chlorpromazine and biological and metal compounds. Furthermore, the Cu₃Mo₂O₉/RGO/SPCE sensor displayed satisfactory recoveries for real-time monitoring of PMH in human urine and serum samples. This study delivers a promising electrochemical sensor for the efficient analysis of antipsychotic drug molecules. Full article

The growing global burden of diabetes necessitates the development of glucose sensors that are not only reliable and sensitive but also cost-effective and amenable to point-of-care use. In this work, we report a non-enzymatic electrochemical glucose sensor based on laser-induced graphene (LIG), functionalized with zinc oxide (ZnO) and palladium (Pd) nanostructures. The ZnO nanostructures were systematically optimized on the LIG surface by varying electrochemical deposition parameters, including applied potential, temperature, and deposition time, to enhance the electrocatalytic oxidation of glucose in alkaline medium. Subsequent modification with Pd nanostructures further improved the electrocatalytic activity and sensitivity of the sensor. The performance of the LIG/ZnO/Pd sensor was investigated using chronoamperometric and cyclic voltammetric analysis in 0.1 M NaOH at an applied potential of 0.65 V. The sensor exhibited a wide dynamic range (2–10 mM; 10–24 mM) with a limit of detection of 130 μM, capturing hypo- and hyperglycemia conditions. Moreover, a sensitivity of 25.63 µA·mM⁻¹·cm⁻² was observed. Additionally, the sensor showcased selective response towards glucose in the presence of common interferents. These findings highlight the potential of the LIG/ZnO/Pd platform for integration into next-generation, non-enzymatic glucose monitoring systems for clinical and point-of-care applications. Full article

A new voltammetric sensor (BDDE/Nafion@Fe₃O₄/BiF) was fabricated by applying a nanocomposite drop of Fe₃O₄ magnetic nanoparticles in Nafion onto the polished boron-doped diamond electrode (BDDE) surface. Then, after drying (5 min at room temperature), the electrode was electrochemically modified with bismuth film (BiF) during in situ analysis. The Nafion@Fe₃O₄/BiF modification of the BDDE contributes to the acquisition of the highest differential-pulse adsorptive stripping voltammetric (DPAdSV) signals of caffeine (CAF) due to the improvement of electron transfer and the increase in the number of active sites on which CAF can be adsorbed. The DPAdSV signals exhibited a linearly varied oxidation peak with the CAF concentration range between 0.5 and 10,000 nM, leading to the 0.043 and 0.14 nM detection and quantification limits, respectively. The practical applicability of the DPAdSV procedure using the BDDE/Nafion@Fe₃O₄/BiF was positively confirmed with commercially available energy drinks. Full article

This study presents the electrochemical detection of caffeic acid using an ester (Diethyl 3,4-dihydroxythiophene-2,5-dicarboxylate)-modified carbon paste electrode (EMCPE). Caffeic acid, a naturally occurring hydroxycinnamic acid with antioxidant properties, was investigated due to its significance in food products and its potential health benefits. The modified electrode demonstrated enhanced sensitivity and selectivity for caffeic acid detection. Voltammetric methods were applied to evaluate the electrode performance. Results indicated that EMCPE has improved electron transfer kinetics and a lower detection limit compared unmodified electrode. Detection and quantification thresholds (LOD and LOQ) were found to be $3.12\times {10}^{-6}$ M and $1.04\times {10}^{-3}$ M. Density functional theory used to understand the electron transfer properties of Diethyl 3,4-dihydroxythiophene-2,5-dicarboxylate. The study highlights the potential of EMCPE as a reliable and cost-effective sensor to quantify caffeic acid across different sample matrices. 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

Flow injection analysis (FIA) is widely used in drug screening, neurotransmitter detection, and water analysis. In this study, we investigated the electrochemical sensing performance of glassy graphene electrodes derived from pyrolyzed positive photoresist films (PPFs) via rapid thermal annealing (RTA) on SiO₂/Si and polycrystalline diamond (PCD). Glassy graphene films fabricated at 800, 900, and 950 °C were characterized using Raman spectroscopy, scanning electron microscopy (SEM), and atomic force microscopy (AFM) to assess their structural and morphological properties. Electrochemical characterization in phosphate-buffered saline (PBS, pH 7.4) revealed that annealing temperature and substrate type influence the potential window and double-layer capacitance. The voltammetric response of glassy graphene electrodes was further evaluated using the surface-insensitive [Ru(NH₃)₆]^3+/2+ redox marker, the surface-sensitive [Fe(CN)₆]^3−/4− redox couple, and adrenaline, demonstrating that electron transfer efficiency is governed by annealing temperature and substrate-induced microstructural changes. FIA with amperometric detection showed a linear electrochemical response to adrenaline in the 3–300 µM range, achieving a low detection limit of 1.05 µM and a high sensitivity of 1.02 µA cm⁻²/µM. These findings highlight the potential of glassy graphene as a cost-effective alternative for advanced electrochemical sensors, particularly in biomolecule detection and analytical applications. Full article

An effective deposition of a cinchonine layer on a platinum metal surface can be easily achieved through the cathodic reduction of a cinchonine hydrochloride methanolic solution at a controlled potential of −220 mV vs. the silver standard electrode (SSE). A coated screen-printed platinum electrode has proven to be suitable for cinchonine determination in water, urine, and serum at µg L⁻¹ concentration levels using differential pulse voltammetry in a phosphate buffer solution (pH 7.0). The limits of detection (LOD) and quantitation (LOQ) were 0.6 µg L⁻¹ and 1.8 µg L⁻¹, respectively. Full article

This review concentrates on the application of carbon-based materials in the development and fabrication of voltammetric sensors of antidepressant drugs used in the treatment of moderate to severe depression, anxiety disorders, personality disorders, and various phobias. Voltammetric techniques offer outstanding sensitivity and selectivity, accuracy, low detection limit, high reproducibility, instrumental simplicity, cost-effectiveness, and short time of direct determination of antidepressant drugs in pharmaceutical and clinical samples. Moreover, the combination of voltammetric approaches with the unique characteristics of carbon and its derivatives has led to the development of powerful electrochemical sensing tools for detecting antidepressant drugs, which are highly desirable in healthcare, environmental monitoring, and the pharmaceutical industry. In this review, carbon-based materials, such as glassy carbon and boron-doped diamond, and a wide spectrum of carbon nanoparticles, including graphene, graphene oxides, reduced graphene oxides, single-walled carbon nanotubes, and multi-walled carbon nanotubes were described in terms of the sensing performance of agomelatine, alprazolam, amitriptyline, aripiprazole, carbamazepine, citalopram, clomipramine, clozapine, clonazepam, desipramine, desvenlafaxine, doxepin, duloxetine, flunitrazepam, fluoxetine, fluvoxamine, imipramine, nifedipine, olanzapine, opipramol, paroxetine, quetiapine, serotonin, sertraline, sulpiride, thioridazine, trazodone, venlafaxine, and vortioxetine. Full article

In the present work, we designed a straightforward and disposable voltammetric sensor utilizing a molybdenum disulfide/multi-walled carbon nanotube nanostructure-modified screen-printed carbon electrode (MoS₂/MWCNTs/SPCE) for 4-nitrophenol (4-NP) determination. The successful synthesis of the MoS₂/MWCNT nanostructure was characterized using Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EXD) mapping. The electrochemical behavior of 4-NP at the MoS₂/MWCNTs/SPCE was examined using differential pulse voltammetry (DPV), cyclic voltammetry (CV), and chronoamperometry techniques. The MoS₂/MWCNTs/SPCE exhibited outstanding electro-catalytic activity for the voltammetric detection of 4-NP. Under optimized conditions, the reduction peak current showed a linear dependence with the concentration of 4-NP in the range of 0.05 to 800.0 µM, and a detection limit (LOD) of 0.01 µM was determined. In addition, the MoS₂/MWCNTs/SPCE sensor has advantages including repeatability, reproducibility, stability, inexpensiveness, and practical application. The MoS₂/MWCNTs/SPCE-based sensor was also utilized for the determination of 4-NP in real water specimens. Full article

This paper shows the fabrication of a new environmentally friendly sensor, an activated glassy carbon electrode with an in situ deposited bismuth film (aGCE/BiF), to determine Cd(II) and Pb(II) at the nanotrace level. The electrochemical activation of the GCE surface was achieved in a solution of 0.1 M phosphate-buffered saline (PBS) of pH = 7 by performing five cyclic voltammetric scans in the range of −1.5–2.5 V at ν of 100 mV/s. The newly developed electrode provides several advantages, such as an increased electron active surface (compared to the glassy carbon electrode) and improved electron transfer kinetics. As a result, the new voltammetric procedure (square-wave anodic stripping voltammetry, SWASV) was established and optimized. With the SWASV method, the following calibration curves and low detection limits (LODs) were obtained for Cd(II) and Pb(II), respectively: 5–100 nM, 0.62 nM, 2–200 nM, and 0.18 nM. The newly prepared method was used to determine the amounts of Pb(II) and Cd(II) in the certified reference material, and the results agreed with the certified values. Moreover, the procedure was successfully applied to determine the Cd(II) and Pb(II) in river samples. The official and standard addition methods validated the measurement results. Full article

Vitamin C, an antioxidant in most fruits and vegetables, is highly sensitive to heat, pH, metals, light, and oxidation, making it a key marker for nutrient degradation in thermal processing. Research aimed at improving processing methods to maximize vitamin C retention is usually limited to expensive laboratory equipment, which does not reflect real-world conditions in the food industry. On the other hand, traditional methods are not suitable for on-line monitoring. This paper proposes bridging the gap in liquid food processing with a voltammetric sensor based on poly(3,4-ethylenedioxythiophene)-modified screen-printed carbon electrodes. The sensor showed excellent repeatability, with intra-sensor RSD below 5% and inter-sensor RSD below 10% at 250 mg/L of ascorbic acid. Detection and quantification limits were 0.7 and 2.1 mg/L, respectively. Trueness assessment in commercial orange juice with a declared vitamin C content yielded a recovery rate of 94 ± 1%. Selectivity tests with citric acid at concentrations equal to and 20 times higher than that of ascorbic acid showed no significant interference. Shelf-life studies confirmed the stability of the sensor for at least two months. This nanocomposite-based approach balances performance and cost with simple preparation, affordable materials, and a stable coating that allows long-term storage in uncontrolled environments. Full article