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Microbial mediator biosensors for surface water toxicity determination make it possible to carry out an early assessment of the environmental object’s quality without time-consuming standard procedures based on standard test-organisms, and provide broad opportunities for receptor element modifying depending on the required operational parameters analyzer. Four microorganisms with broad substrate specificity and nine electron acceptors were used to form a receptor system for toxicity assessment. Ferrocene was the most effective mediator according to its high rate constant of interaction with the microorganisms (0.33 ± 0.01 dm3/(g × s) for yeast Saccharomyces cerevisiae). Biosensors were tested on samples containing four heavy metal ions (Cu2+, Zn2+, Pb2+, Cd2+), two phenols (phenol and p-nitrophenol), and three natural water samples. The «ferrocene- Escherichia coli» and «ferrocene-Paracoccus yeei, E. coli association» systems showed good operational stability with a relative standard deviation of 6.9 and 7.3% (14 measurements) and a reproducibility of 7 and 5.2% using copper (II) ions as a reference toxicant. Biosensor analysis with these systems was shown to highly correlate with the results of the standard method using Chlorella algae as a test object. Developed biosensors allow for a valuation of the polluted natural water’s impact on the ecosystem via an assessment of the influence on bacteria and yeast in the receptor system. The systems could be used in toxicological monitoring of natural waters.

This work proposes an approach to the formation of receptor elements for the rapid diagnosis of the state of surface waters according to two indicators: the biochemical oxygen demand (BOD) index and toxicity. Associations among microorganisms based on the bacteria P. yeei and yeast S. cerevisiae, as well as associations of the yeasts O. polymorpha and B. adeninivorans, were formed to evaluate these indicators, respectively. The use of nanocomposite electrically conductive materials based on carbon nanotubes, biocompatible natural polymers—chitosan and bovine serum albumin cross-linked with ferrocenecarboxaldehyde, neutral red, safranin, and phenosafranin—has made it possible to expand the analytical capabilities of receptor systems. Redox polymers were studied by IR spectroscopy and Raman spectroscopy, the contents of electroactive components were determined by atomic absorption spectroscopy, and electrochemical properties were studied by electrochemical impedance and cyclic voltammetry methods. Based on the proposed kinetic approach to modeling individual stages of bioelectrochemical processes, the chitosan–neutral red/CNT composite was chosen to immobilize the yeast association between O. polymorpha (ks = 370 ± 20 L/g × s) and B. adeninivorans (320 ± 30 L/g × s), and a bovine serum albumin (BSA)–neutral composite was chosen to immobilize the association between the yeast S. cerevisiae (ks = 130 ± 10 L/g × s) and the bacteria P. yeei red/CNT (170 ± 30 L/g × s). After optimizing the composition of the receptor systems, it was shown that the use of nanocomposite materials together with associations among microorganisms makes it possible to determine BOD with high sensitivity (with a lower limit of 0.6 mg/dm3) and detect the presence of a wide range of toxicants of both organic and inorganic origin. Both receptor elements were tested on water samples, showing a high correlation between the results of biosensor analysis of BOD and toxicity and the results of standard analytical methods. The results obtained show broad prospects for creating sensitive and portable bioelectrochemical sensors for the early warning of environmentally hazardous situations based on associations among microorganisms and nanocomposite materials.

Diabetes mellitus is a pathological condition that requires continuous measurement of glucose concentration in human blood. In this study, two enzymatic mediator-free glucose biosensors based on premodified graphite rod (GR) electrodes were developed and compared. GR electrode modified with electrochemically synthesized dendritic gold nanostructures (DGNS), a cystamine (Cys) self-assembled monolayer (SAM), and glucose oxidase (GOx) (GR/DGNS/Cys/GOx) and GR electrode modified with DGNS, Cys SAM, enzymatically obtained polyaniline (PANI) nanocomposites with embedded 6 nm gold nanoparticles (AuNPs) and GOx (GR/DGNS/Cys/PANI-AuNPs-GOx/GOx) were investigated electrochemically. Biosensors based on GR/DGNS/Cys/GOx and GR/DGNS/Cys/PANI-AuNPs-GOx/GOx electrodes were characterized by a linear range (LR) of up to 1.0 mM of glucose, storage stability of over 71 days, sensitivity of 93.7 and 72.0 μA/(mM cm2), limit of detection (LOD) of 0.027 and 0.034 mM, reproducibility of 13.6 and 9.03%, and repeatability of 8.96 and 8.01%, respectively. The GR/DGNS/Cys/PANI-AuNPs-GOx/GOx electrode was proposed as more favorable for glucose concentration determination in serum due to its better stability and resistance to interfering electrochemically active species. The technological solutions presented in this paper are expected to enable the development of innovative mediator-free enzymatic glucose biosensors, offering advantages for clinical assays, particularly for controlling blood glucose concentration in individuals with diabetes.

We developed a wireless monitoring system to monitor fish condition by tracking the change in whole cholesterol concentration. The whole cholesterol concentration of fish is a source of steroid hormones or indicator of immunity level, which makes its detection important for tracking physiological condition of fish. Wireless monitoring system comprises of mediator-type biosensor and wireless transmission device. Biosensor is implantable to fish body, and transmission device is so light, in that fish is allowed to swim freely during monitoring. Cholesterol esterase and oxidase were fixated on to the detection site of biosensor and used to detect the whole cholesterol concentration. However, cholesterol oxidase incorporates oxidation–reduction reaction of oxygen for detection, which concentration fluctuates easily due to change in environmental condition. Meanwhile, mediator-type biosensor enables monitoring of whole cholesterol concentration by using mediator to substitute that oxidation–reduction reaction of oxygen. Characteristic of fabricated mediator-type biosensor was tested. The sensor output current of mediator-type biosensor remained stable compared to output current of non-mediator-type biosensor under fluctuating oxygen concentration of 0–8 ppm, which implied that this sensor is less affected by change in dissolved oxygen concentration. That biosensor was then implanted into fish for wireless monitoring. As a result, approximately 48 h of real-time monitoring was successful.

In the past few decades, biosensors have been gradually developed for the rapid detection and monitoring of human diseases. Recently, functional nucleic-acid (FNA) biosensors have attracted the attention of scholars due to a series of advantages such as high stability and strong specificity, as well as the significant progress they have made in terms of biomedical applications. However, there are few reports that systematically and comprehensively summarize its working principles, classification and application. In this review, we primarily introduce functional modes of biosensors that combine functional nucleic acids with different signal output modes. In addition, the mechanisms of action of several media of the FNA biosensor are introduced. Finally, the practical application and existing problems of FNA sensors are discussed, and the future development directions and application prospects of functional nucleic acid sensors are prospected.

The possibility of the developing a biochemical oxygen demand (BOD) biosensor based on electroactive biofilms of activated sludge grown on the surface of a graphite-paste electrode modified with carbon nanotubes was studied. A complex of microscopic methods controlled biofilm formation: optical microscopy with phase contrast, scanning electron microscopy, and laser confocal microscopy. The features of charge transfer in the obtained electroactive biofilms were studied using the methods of cyclic voltammetry and electrochemical impedance spectroscopy. The rate constant of the interaction of microorganisms with the extracellular electron carrier (0.79 ± 0.03 dm3(g s)−1) and the heterogeneous rate constant of electron transfer (0.34 ± 0.02 cm s−1) were determined using the cyclic voltammetry method. These results revealed that the modification of the carbon nanotubes’ (CNT) electrode surface makes it possible to create electroactive biofilms. An analysis of the metrological and analytical characteristics of the created biosensors showed that the lower limit of the biosensor based on an electroactive biofilm of activated sludge is 0.41 mgO2/dm3, which makes it possible to analyze almost any water sample. Analysis of 12 surface water samples showed a high correlation (R2 = 0.99) with the results of the standard method for determining biochemical oxygen demand.

This review provides a general overview of different biosensors, mostly concentrating on electrochemical analytical devices, while briefly explaining general approaches to various kinds of biosensors, their construction and performance. A discussion on how all required components of biosensors are brought together to perform analytical work is offered. Different signal-transducing mechanisms are discussed, particularly addressing the immobilization of biomolecular components in the vicinity of a transducer interface and their functional integration with electronic devices. The review is mostly addressing general concepts of the biosensing processes rather than specific modern achievements in the area.

Hydrophilic polymer–osmium complexes enhance electron transfer between enzymes and electrodes in biosensors. In this study, hydrophobic poly(4-vinylpyridine) (PVP) was quaternized with 2-bromoethanol to synthesize water-soluble PVP(Q)-C2H4OH polymers (MW 60,000 and 160,000). The resulting PVP(Q)-C2H4OH-Os(dmo-bpy)2Cl complexes were verified by UV-Vis, FT-IR, 1H NMR, SEM-EDS, and zeta potential analyses, confirming successful quaternization and osmium coordination with good dispersion stability. Electrochemical tests (cyclic voltammetry, multi-potential step, amperometry) demonstrated that electrodes with quaternized mediators showed greatly enhanced catalytic currents for glucose (0–20 mM), with sensitivities of 6.9791 (MW 60,000) and 6.6279 μA·mM−1·cm−2 (MW 160,000), respectively, which were 6.6–10.3 times higher than those of non-quaternized polymers. Selectivity tests showed negligible interference from common species such as ascorbic acid, dopamine, uric acid, and serotonin. Continuous glucose monitoring (CGM) electrodes were fabricated by immobilizing the mediator and glucose dehydrogenase on silanized Au electrodes. SEM, scan rate, and impedance analyses confirmed stable binding. The modified electrodes showed strong linearity (R2 = 0.992) and high sensitivity (2.56 μA·mM−1·cm−2), and good stability, maintaining ~82% activity for seven days. Human plasma testing validated accurate glucose detection (6.05 mM), consistent with physiological levels. Overall, quaternized PVP(Q) mediators significantly improved solubility and electron transfer, enabling the development of a stable, selective glucose sensor suitable for CGM applications.

Herein, an electrochemical biosensor based on carbon nanofibers (CNF) and ferrocene carboxylic acid (FcA) modified glassy carbon electrode (GCE) was fabricated for xanthine determination. Xanthine oxidase (XO) was further immobilized onto the FcA/CNF/GCE for the fabrication of the biosensor. The morphologic appearance of the XO/FcA/CNF/GCE was studied by scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) measurements were also performed to determine the electrochemical characteristics of the modified electrode. The XO/FcA/CNF/GCE biosensor exhibited linear response for xanthine in the concentration range of 6.0 × 10 –7 to 2.0 × 10 –4  M with a sensitivity of 6.04 µAmM −1 and a detection limit of 1.7 × 10 –7  M. The xanthine biosensor also exhibited the advantages of high reproducibility, anti-interference ability and good long-term stability. Furthermore, the XO/FcA/CNF/GCE was used for the determination of xanthine in fish meat and the satisfactory results indicated that the FcA/CNF matrix is a promising candidate for electrode modification.

Electrochemical DNA sensors represent a simple, accurate and economical platform for DNA detection. Gold nanoparticles are known to be efficient labels in electrochemical sensors and to be viable materials to modify the surface of electrodes thereby to enhance the detection limit of the sensor. For surface modification, gold nanoparticles are used in combination with nanomaterials like graphene, graphene oxide, or carbon nanotubes to improve electrochemical performance in general. This review (with 116 refs.) mainly covers the advances made in recent years in the use of gold nanoparticles in DNA sensing. It is divided into the following main sections: (a) An introduction covers aspects of electrochemical sensing of DNA and of appropriate nanomaterials in general. (b) The use of gold nanoparticles in DNA is specifically addressed next, with subsections on AuNPs acting as electrochemical labels, electron transfer mediators, signal amplifiers, carriers of electroactive molecules, catalysts, immobilization platforms, on silver enhancement strategies, on AuNPs modified with carbonaceous materials (such as graphenes and nanotubes), and on multiple amplification schemes. The review concludes with a discussion of current challenges and trends in terms of highly sensitive DNA based sensing using AuNPs. Graphical abstract The review describes the state of the art in the use of gold nanoparticles in the electrochemical DNA sensors and contains sections on the use of AuNPs as labels, signal amplifiers, carriers of electroactive molecules, catalyst, immobilization platform, and on silver enhancement and multiple amplification strategies.