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The interactions of compounds with DNA have been studied since the recognition of the role of nucleic acid in organisms. The design of molecules which specifically interact with DNA sequences allows for the control of the gene expression. Determining the type and strength of such interaction is an indispensable element of pharmaceutical studies. Cognition of the therapeutic action mechanisms is particularly important for designing new drugs. Owing to their sensitivity, simplicity, and low costs, electrochemical methods are increasingly used for this type of research. Compared to other techniques, they require a small number of samples and are characterized by a high reliability. These methods can provide information about the type of interaction and the binding strength, as well as the damage caused by biologically active molecules targeting the cellular DNA. This review paper summarizes the various electrochemical approaches used for the study of the interactions between pharmaceuticals and DNA. The main focus is on the papers from the last decade, with particular attention on the voltammetric techniques. The most preferred experimental approaches, the electrode materials and the new methods of modification are presented. The data on the detection ranges, the binding modes and the binding constant values of pharmaceuticals are summarized. Both the importance of the presented research and the importance of future prospects are discussed.

Developing ultrasensitive and user-friendly methods for the detection glucose has attracted more and more attention. By virtue of high selectivity and sensitivity, enzyme-based glucose sensor plays a key role in point-of-care sensing technology for detecting glucose concentration. In this study, Amplex Red (AR), as both indicator and mediator, was investigated to detect glucose in presence of glucose oxidase (GOx) enzymes using colorimetric and electrochemical methods. Without using any advanced techniques and sophisticated nanomaterials, 1 μM glucose can be easily detected through simply detecting the solution color with a visual colorimetric method. On the other hand, the electrochemical method can provide much higher sensitivity for the detection of glucose, which achieves a linear range spanning from 20 nM to 3.56 μM with a limit of 7.3 nM (signal-to-noise ratio SNR = 3). It is also found that the presence of other sugars such as fructose, lactose, and maltose have very limited interference effects on the detection of glucose. More importantly, a bare GC electrode was used in all these electrochemical measurements without any electrode surface modification, guaranteeing a simple and fast operation. The analytical platforms for the detection of glucose presented here not only provide simple, fast, and ultrasensitive methods, but also have the potential to advance the sensing technology in the application of other health diagnostic research areas.

We have prepared a kind of molecularly imprinted nano-porous sensing film for the adsorption of melamine. It consists of a graphite electrode impregnated with paraffin and modified with melamine, chitosan, silver nanoparticles and polyquercetin by employing an electrochemical method. The film displays excellent and highly selective sorption of melamine in the 3-dimensional porous nanomaterial, and this was applied to the determination of melamine in dairy products. The electrode responds linearly to melamine in the concentration range of 1 × 10 −8 to 9 × 10 −7  M, with a detection limit of 1.3 × 10 −9  M (at 3σ) in real samples, and with recoveries in the range of 99 to 102%. The surface structure and composition of the sensor was characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, infrared spectroscopy, and electrochemical techniques. The interaction between the porous film and melamine was also studied by using hexacyanoferrate (III) as an electrochemical indicator. Figure Extremely sensitive sensor for melamine used a kind of molecularly mprinted nano-porous film, which displays an excellent and highly selective sorption to melamine in the 3-dimensional porous nanomaterial. The interaction between the porous film and melamine also was studied by using hexacyanoferrate (III) as an electrochemical indicator.

A promising electrochemical strategy for assay of N6-methyladenosine (m6A)/N6-methyladenine (6mA) in RNA/DNA is proposed. The key of this strategy is the end-labeling of nucleic acid, which makes it possible to detect methylation level in unknown sequence. Firstly, the end of m6A-RNA or 6mA-DNA was labeled with sulfhydryl group through T4 polynucleotide kinase (T4 PNK) and then directly assembled on a gold nanoparticle–modified glassy carbon electrode (AuNPs/GCE). Secondly, methylation sites in RNA/DNA were specifically recognized by anti-m6A-antibody, and then, horseradish peroxidase–labeled goat anti-rabbit IgG (HRP-IgG) was further conjugated on the antibody. Thirdly, HRP-IgG catalyzed the hydroquinone oxidation reaction to generate amplified current signal which correlates with the amount of m6A/6mA in nucleic acid. This method showed a wide linear range from 0.0001 to 10 nM for m6A-RNA, 0.001 to 100 nM for 6mA-dsDNA, and 0.0001 to 10 nM for 6mA-ssDNA. The method was successfully applied to detection of m6A/6mA in RNA/DNA from HeLa cells and E. coli cells and validation of the decrease of m6A-RNA in HeLa cells after treatment with FTO protein. Graphical abstract

Electrochemical methods, particularly when applied in connection with mercury-containing electrodes, are excellent tools for studying nucleic acids structure and monitoring structural transitions. We studied the effect of the length of the central (dG) ₙ stretch (varying from 0 to 15 guanine residues) in 15-mer oligodeoxynucleotides (ODN, G0 to G15) on their electrochemical and interfacial behavior at mercury and carbon electrodes. The intensity of guanine oxidation signal at the carbon electrode (peak Gᵒˣ) was observed to increase continuously with number of guanines between 0 and 15, with only a slight positive shift for ODNs with seven or more guanines in the central segment. Very different effects were observed when the peak Gᴴᴹᴰᴱ was measured at the mercury electrode. Intensity of the latter signal increased with number of guanines up to G5, and decreased sharply with further elongation of the (dG) ₙ stretch. CD spectroscopy and electrophoresis experiments revealed formation of parallel intermolecular quadruplex structures for ODNs containing five or more G residues. Further measurements made by cyclic and alternating-current voltammetry revealed a strong influence of the ODN structure on their behavior at electrically charged surfaces.

The creation and analysis of a large variety of existing methods for the evaluation of integrated antioxidant properties are quite relevant in connection with a range of biological mechanisms of the antioxidants (AO) action. In this work, the existing methods are correlated with mechanisms of antioxidant action. It is shown that the results obtained by various methods are mainly incomparable. This can be connected with the implementation of various mechanisms of antioxidant action in methods. The analysis of the literature data presented in this review indicates the difficulty of creating a universal method and the feasibility of using integrated approaches based on the use of several methods that implement and combine various mechanisms of the chemical conversion of antioxidants. This review describes methods for studying the chelating ability of antioxidants, except for methods based on electron and hydrogen atom transfer reactions, which are currently not widely covered in modern literature. With the description of each mechanism, special attention is paid to electrochemical methods, as the interaction of active oxygen metabolites of radical and non-radical nature with antioxidants has an electron/proton/donor-acceptor nature, which corresponds to the nature of electrochemical methods and suggests that they can be used to study the interaction.

Heavy metal ions, one of the major pollutants in the environment, exhibit non-degradable and bio-chain accumulation characteristics, seriously damage the environment, and threaten human health. Traditional heavy metal ion detection methods often require complex and expensive instruments, professional operation, tedious sample preparation, high requirements for laboratory conditions, and operator professionalism, and they cannot be widely used in the field for real-time and rapid detection. Therefore, developing portable, highly sensitive, selective, and economical sensors is necessary for the detection of toxic metal ions in the field. This paper presents portable sensing based on optical and electrochemical methods for the in situ detection of trace heavy metal ions. Progress in research on portable sensor devices based on fluorescence, colorimetric, portable surface Raman enhancement, plasmon resonance, and various electrical parameter analysis principles is highlighted, and the characteristics of the detection limits, linear detection ranges, and stability of the various sensing methods are analyzed. Accordingly, this review provides a reference for the design of portable heavy metal ion sensing.

Water pollution by recalcitrant compounds is an increasingly important problem due to the continuous introduction of new chemicals into the environment. Choosing appropriate measures and developing successful strategies for eliminating hazardous wastewater contaminants from industrial processes is currently a primary goal. Electroplating industry wastewater involves highly toxic cyanide (CN), heavy metal ions, oils and greases, organic solvents, and the complicated composition of effluents and may also contain biological oxygen demand (BOD), chemical oxygen demand (COD), SS, DS, TS, and turbidity. The availability of these metal ions in electroplating industry wastewater makes the water so toxic and corrosive. Because these heavy metals are harmful to living things, they must be removed to prevent them from being absorbed by plants, animals, and humans. As a result, exposure to electroplating wastewater can induce necrosis and nephritis in humans and lung cancer, digestive system cancer, anemia, hepatitis, and maxillary sinus cancer with prolonged exposure. For the safe discharge of electroplating industry effluents, appropriate wastewater treatment has to be provided. This article examines and assesses new approaches such as coagulation and flocculation, chemical precipitation, ion exchange, membrane filtration, adsorption, electrochemical treatment, and advanced oxidation process (AOP) for treating the electroplating industry wastewater. On the other hand, these physicochemical approaches have significant drawbacks, including a high initial investment and operating cost due to costly chemical reagents, the production of metal complexes sludge that needs additional treatment, and a long recovery process. At the same time, advanced techniques such as electrochemical treatment can remove various kinds of organic and inorganic contaminants such as BOD, COD, and heavy metals. The electrochemical treatment process has several advantages over traditional technologies, including complete removal of persistent organic pollutants, environmental friendliness, ease of integration with other conventional technologies, less sludge production, high separation, and shorter residence time. The effectiveness of the electrochemical treatment process depends on various parameters, including pH, electrode material, operation time, electrode gap, and current density. This review mainly emphasizes the removal of heavy metals and another pollutant such as CN from electroplating discharge. This paper will be helpful in the selection of efficient techniques for treatment based on the quantity and characteristics of the effluent produced.

This study aimed to analyze and evaluate the performance of surface and corrosion behavior of SMA steel exposed to alkaline solutions. The initial characteristics were performed using scanning electron microscopy (SEM). The corrosion resistance performance of SMA steel with varying carbon composition with and without 30% strain in different alkaline environments (pH 14, pH 10, and pH 8) was investigated using electrochemical methods. The change in surface morphology and chemical composition was analyzed using SEM-EDAX, AFM, EDX, and XPS. The test results showed that the performance of SMA steel in an alkaline environment was affected by carbon content and the 30% strain process. Higher carbon content and 30% strain treatment caused an increase in corrosion rate. The highest corrosion rate in SMA steel with a content of 0.39% C with a pre-strain was obtained at 5.87 mpy. In addition, the pH level of the solution significantly affects the cycling behavior and surface morphology of shape memory alloy steels in alkaline solutions. The cycling behavior is relatively stable, with minimal corrosion damage in high alkaline (pH 14) and moderate alkaline (pH 10) conditions. Meanwhile, in slightly alkaline solutions (pH 8), aggressive damage to the oxide layer and local corrosion occurs.

Electrochemical impedance spectroscopy is finding increasing use in electrochemical sensors and biosensors, both in their characterisation, including during successive phases of sensor construction, and in application as a quantitative determination technique. Much of the published work continues to make little use of all the information that can be furnished by full physical modelling and analysis of the impedance spectra, and thus does not throw more than a superficial light on the processes occurring. Analysis is often restricted to estimating values of charge transfer resistances without interpretation and ignoring other electrical equivalent circuit components. In this article, the important basics of electrochemical impedance for electrochemical sensors and biosensors are presented, focussing on the necessary electrical circuit elements. This is followed by examples of its use in characterisation and in electroanalytical applications, at the same time demonstrating how fuller use can be made of the information obtained from complete modelling and analysis of the data in the spectra, the values of the circuit components and their physical meaning. The future outlook for electrochemical impedance in the sensing field is discussed.