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This review provides an overview of recent advances in electrochemical sensors for analyte detection in saliva, highlighting their potential applications in diagnostics and health care. The purpose of this paper is to summarize the current state of the field, identify challenges and limitations and discuss future prospects for the development of saliva-based electrochemical sensors.

The paper reviews relevant literature and research articles to examine the latest developments in electrochemical sensing technologies for saliva analysis. It explores the use of various electrode materials, including carbon nanomaterial, metal nanoparticles and conducting polymers, as well as the integration of microfluidics, lab-on-a-chip (LOC) devices and wearable/implantable technologies. The design and fabrication methodologies used in these sensors are discussed, along with sample preparation techniques and biorecognition elements for enhancing sensor performance.

Electrochemical sensors for salivary analyte detection have demonstrated excellent potential for noninvasive, rapid and cost-effective diagnostics. Recent advancements have resulted in improved sensor selectivity, stability, sensitivity and compatibility with complex saliva samples. Integration with microfluidics and LOC technologies has shown promise in enhancing sensor efficiency and accuracy. In addition, wearable and implantable sensors enable continuous, real-time monitoring of salivary analytes, opening new avenues for personalized health care and disease management.

This review presents an up-to-date overview of electrochemical sensors for analyte detection in saliva, offering insights into their design, fabrication and performance. It highlights the originality and value of integrating electrochemical sensing with microfluidics, wearable/implantable technologies and point-of-care testing platforms. The review also identifies challenges and limitations, such as interference from other saliva components and the need for improved stability and reproducibility. Future prospects include the development of novel microfluidic devices, advanced materials and user-friendly diagnostic devices to unlock the full potential of saliva-based electrochemical sensing in clinical practice.

The purpose of this study is to develop a molecular imprinting electrochemical sensor for the specific detection of the anticancer drug amsacrine. The sensor used a composite of bacterial cellulose (BC) and silver nanoparticles (AgNPs) as a platform for the immobilization of a molecularly imprinted polymer (MIP) film. The main objective was to enhance the electrochemical properties of the sensor and achieve a high level of selectivity and sensitivity toward amsacrine molecules in complex biological samples.

The composite of BC-AgNPs was synthesized and characterized using FTIR, XRD and SEM techniques. The MIP film was molecularly imprinted to selectively bind amsacrine molecules. Electrochemical characterization, including cyclic voltammetry and electrochemical impedance spectroscopy, was performed to evaluate the modified electrode’s conductivity and electron transfer compared to the bare glassy carbon electrode (GCE). Differential pulse voltammetry was used for quantitative detection of amsacrine in the concentration range of 30–110 µM.

The developed molecular imprinting electrochemical sensor demonstrated significant improvements in conductivity and electron transfer compared to the bare GCE. The sensor exhibited a linear response to amsacrine concentrations between 30 and 110 µM, with a low limit of detection of 1.51 µM. The electrochemical response of the sensor showed remarkable changes before and after amsacrine binding, indicating the successful imprinting of amsacrine in the MIP film. The sensor displayed excellent selectivity for amsacrine in the presence of interfering substances, and it exhibited good stability and reproducibility.

This study presents a novel molecular imprinting electrochemical sensor design using a composite of BC and AgNPs as a platform for MIP film immobilization. The incorporation of BC-AgNPs improved the sensor’s electrochemical properties, leading to enhanced sensitivity and selectivity for amsacrine detection. The successful imprinting of amsacrine in the MIP film contributes to the sensor's specificity. The sensor's ability to detect amsacrine in a concentration range relevant to anticancer therapy and its excellent performance in complex sample matrices add significant value to the field of electrochemical sensing for pharmaceutical analysis.

This paper aims to access the protective function of hybrid sol-gel coatings deposited on 304L stainless steel substrate in silane solutions containing a mixture of tetraethoxysilane, methyltriethoxysilane and glycidyloxypropyltrimethoxysilane with different pH values during various immersion periods.

The 304L stainless steels coated through 10 and 30 s of immersion in the silane solutions with pH values of 2.1 and 2.8 were exposed to NaCl solution. The corrosion resistance of the coated substrates was studied through taking advantage of electrochemical noise method as well as atomic force microscopy (AFM), water contact angle and field emission-type scanning electron microscopy (FESEM) surface analysis.

The electrochemical current noise, PSD (I) plot, noise resistance and characteristic charge as parameters extracted from electrochemical noise method indicated the superiority of eco-friendly silane coating deposited on the substrate surface during 10 s exposure to the solution, due to the film uniformity and homogeneity as confirmed by FESEM and AFM. Moreover, immersion of the stainless steel in the silane solution with pH 2.1, characterized by higher hydrolysis ratio, led to more effective corrosion control in the NaCl electrolyte according to the results of electrochemical noise and FTIR measurements.

The noise resistance and characteristic charge as electrochemical noise parameters were only used in this research to evaluate the protective behavior of the water-based silane sol-gel coatings. Future studies should examine the correlation between electrochemical noise data and the parameters extracted from other electrochemical methods, e.g. electrochemical impedance spectroscopy.

The data obtained in this research may provide an effective approach based on electrochemical noise method to screen the silane sol-gel coatings for protection of metallic substrates against corrosion.

According to the literature, no report can be found studying the effect of immersion time on a silane solution, including glycidyloxypropyltrimethoxysilane, tetraethoxysilane and methyltriethoxysilane, as well as the silane solution pH on the corrosion resistance of 304L stainless steel in NaCl solution through electrochemical noise method.

This review aims to focus on recent reported research work on the construction and function of different electrochemical DNA biosensors. It also describes different sensing materials, chemistries of immobilization probes, conditions of hybridization and principles of transducing and amplification strategies.

The human disease-related mutated genes or DNA sequence detection at low cost can be verified by the electrochemical-based biosensor. A range of different chemistries is used by the DNA-based electrochemical biosensors, out of which the interactions of nanoscale material with recognition layer and a solid electrode surface are most interesting. A diversity of advancements has been made in the field of electrochemical detection.

Some important aspects are also highlighted in this review, which can contribute in the creation of successful biosensing devices in the future.

This paper provides an updated review of construction and sensing technologies in the field of biosensing.

The purpose of the study is to highlight the potential of the sensor based smartphone in assessing the covid-19 cases. Coronavirus disease 2019 (COVID-19) is a noxious pandemic affecting the respiratory system of the human and leading to the severe acute respiratory syndrome, sometimes causing death. COVID-19 is a highly transmittable disease that spreads from an infected person to others. In this regard, a smart device is required to monitor the COVID-19 infected patients by which widespread pandemic can be reduced.

In this paper, an electrochemical sensor-enabled smartphone has been developed to assess the COVID-19 infected patients. The data-enabled smartphone uses the Internet of Things (IoT) to share the details with the other devices. The electrochemical sensor enables the smartphone to evaluate the ribonucleic acid (RNA) of COVID-19 without the nucleic acid and feeds the data into the data server by using a smartphone.

The obtained result identifies the infected person by using the portable electrochemical sensor-enabled smartphone, and the data is feed into the data server using the IoT. Whenever an infected person moves outside the restricted zone, the data server gives information to the concerned department.

The developed electrochemical sensor-enabled smartphone gives an accuracy of 81% in assessing the COVID-19 cases. Thus, through the developed approach, a COVID-19 infected person can be identified and the spread can be minimized.

The purpose of this paper is to investigate, the effects of residual stress and microstructure on the corrosion behaviour of carburised 18CrNiMo7-6 steel in a 3.5% NaCl aqueous solution.

The electrochemical tests were conducted using an electrochemical workstation with a three-electrode system in a 3.5% NaCl aqueous solution, the residual stress of each working face was measured by a high-speed residual stress analyser, and microstructure of different carburised layers were observed scanning electron microscopy. Finally, the effect of carbon content, microstructure and residual stress on the corrosion behaviour of the steel was discussed.

The results showed that the residual compressive stress in the carburised layer initially increased and subsequently decreased with increasing depth of the carburised layer, reaching stability in the matrix layer. The electrochemical tests before and after stress reduction showed that the electrochemical impedance and the electrochemical potential increased with the reduction of residual compressive stress.

The residual compressive stress in the carburised layer initially increases and subsequently decreases with increasing carburised layer depth. The electrochemical impedance and the electrochemical potential increased with the reduction of residual compressive stress. The general relationship between electrochemical potential and residual stress was established.

The purpose of this study is to investigate the effect of Y₂O₃ mass fraction on the electrochemical corrosion performance of CrNi coating, which provided a foundation for the performance optimization of CrNi coatings.

CrNi coatings with the different Y₂O₃ mass fractions were fabricated on AISI H13 steel by laser cladding, and the effect of Y₂O₃ mass fraction on the electrochemical performance of CrNi coating in 3.5% NaCl solution was investigated using an electrochemical workstation.

The electrochemical corrosion performance of CrNi coating enhances with the increase of Y₂O₃ mass fraction, and the CrNi–15%Y₂O₃ coating has the largest polarization resistance and the lowest corrosion current density, which displays the best electrochemical performance among the CrNi–5%Y₂O₃, –10%Y₂O₃ and –15%Y₂O₃ coatings. The protective films are formed with the increase of Y₂O₃ mass fraction, which inhibits the occurrence of electrochemical corrosion.

The Y₂O₃ was first added to the CrNi coating to improve its electrochemical corrosion performance, and the influence of Y₂O₃ on the corrosion resistance of the CrNi coating was discussed by the corrosion model.

The purpose of this paper is to produce non-conductive copolymers of N-vinyl carbazole (NVCz) and methyl ethyl ketone formaldehyde resin (MEKFR) by the electroinduced Ce (IV) polymerization method and the electrochemical oxidization of the formed copolymer to produce their conductive green form. The non-conductive and conductive copolymers were characterized by using Fourier transform infrared, solid-state conductivity and spectroelectrochemical, chronoamperometric, cyclovoltammetric and electrochemical impedance spectroscopic measurements.

The chronoamperometric electropolymerization of white, insulator form of the copolymer of NVCz and MEKFR (copolymer 1) on to Pt electrode was carried out and the green coloured film of the MEKFR-ox-NVCz copolymer (copolymer 11) was produced in the doped and conductive form. All reactions were performed in dichloromethane containing 0.1 M B_U4NClO₄. Copolymer 11 films obtained on the surface of the working electrode were removed and washed in acetonitrile and dried at room temperature before characterization. The results were compared with the copolymer obtained by electrochemical oxidation of MEKF-R and NVCz (copolymer 2).

The insulating copolymer of NVCz and MEKFR (copolymer 1) was produced by the electroinduced Ce (IV) polymerization method and converted into the conductive form electrochemically on the surface of the Pt electrode (copolymer 11). The polymers were characterized by electrochemical, spectrophotometric and conductivity measurements. The ionization potentials, optical band gap, peak potentials Ep, doping degree and specific capacitance of the copolymer 11 were obtained. The conductivity of the copolymer 11 is lower than the PNVCz and higher than the copolymer obtained by electrochemical oxidation of MEKF-R and NVCz (copolymer 2). The copolymer 11 has a lower onset potential than PNVCz and the copolymer 1 and slightly higher band gap than PNVCz. The capacitive behaviours of the copolymer 11 were very close to PNVCz.

This study focuses on obtaining a green and conductive form of the copolymer of NVCz and MEKFR with the electrochemical method by using a white and insulator form of the same copolymer.

This work provides technical information for the synthesis of conducting copolymer of NVCz and MEKFR.

These copolymers may be in the field of PNVCz applications such as photoconductivity and corrosion inhibition.

Electroinduced Ce (IV) MEKFR redox system was applied for the polymerization of NVCz monomer to produce the copolymer 1. The conductive copolymer 11 was synthesized through electrochemical oxidative coupling of the carbazole groups of the copolymer 1.

The purpose of this paper is to report a novel electrochemical sensor designed to detect the corrosion of metal cans used for beverage packaging.

Electrochemical impedance spectroscopy (EIS) and electrochemical noise (EN) were performed to detect the corrosion degree of beverage cans that had been stored for 1 month (named s1), 3 months (named s2), 27 months (named s3) and 43 months (named s4).

The EIS results showed that the EIS plot of s1 samples had not developed to a characteristic of two time‐constants, indicating that the coating showed good protective performance. The EIS plots of s2, s3 and s4 showed characteristics of two time‐constants, indicating that the organic coatings of s2, s3, and s4 had lost their protective performance. EN results showed that quantities and amplitudes of transient peaks increased with the increasing storage time, indicating that an increasing degree of local corrosion occurred within the cans. A corrosion process for beverage cans is discussed and can be considered in three stages.

The designed electrochemical sensor was successfully applied to detect the performance of beverage cans and, further, provided scientific proof to evaluate the shelf life of metal cans for packaging.

An indirect electrochemical reduction and dyeing with indigo were carried out here to solve problems of low dye reduction rate and poor dyeing depth in the current electrochemical dyeing process.

Response surface analysis tests were performed to evaluate the effects of ferrous sulfate concentration, medium concentration, sodium hydroxide concentration and reduction time on the reduction efficiency of indirect electrochemical reduction of indigo.

The conditions obtained by design-expert optimization showed that the concentration of FeSO₄·7H₂O has the most significant effect on the reduction performance of dye liquor. Under the optimized electrochemical reduction dyeing process, the rate of dye reduction could be reached 91.21 per cent and the K/S value of indirect electrochemical dyeing of indigo can be achieved to 12.96, which is increased by about 9.56 per cent compared with that of Na₂S₂O₄ dyeing with the same color fastness basically.

The recyclability and biodegradability of the dye remain to be explored.

The strategy presented here can be developed to replace a substantial part of electrochemical dyeing with optimized product quality and reduced environmental pollution in denim production.

The strategy presented here can be developed to replace a substantial part of electrochemical dyeing with optimized product quality and reduced environmental pollution in denim production.

Application of the Fe(II)-DGS-Abal B complex media system in the indirect electrochemical reduction of indigo.