The detection of environmental toxicants is transitioning from centralized laboratory methods to decentralized, point-of-care (POC) monitoring. A highly innovative approach in this field is the repurposing of commercially available, low-cost, and portable personal glucose meters (PGMs) as universal biosensing platforms. This strategy leverages the widespread availability and ease of use of PGMs to develop rapid, on-site detection methods for a wide array of non-glucose targets, significantly reducing both cost and development time. This systematic review comprehensively examines the various strategies employed to adapt PGMs for the detection of a wide array of ecotoxicants, including chemical targets (antibiotics, mycotoxins, pesticides, heavy metals, persistent organic pollutants) and biological ones (pathogenic bacteria, and viruses). The systematic review critically evaluates different sensor designs, highlighting that while aptamer-based and non-enzymatic biosensors offer advantages in stability and cost, antibody-based sensors provide high specificity. A significant finding is the persistent trade-off between analytical sensitivity and practical field deployment; many of the most sensitive assays require multi-step procedures, precise temperature control, magnetic separation, centrifugation, and the use of additional equipment, factors that undermine true POC utility. To address this gap, we propose four essential criteria for POC readiness: (i) ambient-temperature operation, (ii) no reliance on magnetic or centrifugal separation, (iii) total assay time, and (iv) robustness in complex environmental matrices. This systematic review confirms the feasibility of this approach across a broad spectrum of targets. However, the key challenge for future research lies in simplifying the assay protocols, eliminating cumbersome sample preparation steps, and enhancing robustness to make these biosensors truly practical for routine, on-site environmental monitoring.

This study presents the synthesis of new fluorosulfate derivatives of 1,4-naphthoquinone by the SuFEx reaction. Anticancer properties of obtained compounds were studied on PC-3 (prostate adenocarcinoma), SKOV-3 (ovarian cancer), MCF-7 (breast cancer), and Jurkat cell lines. All the studied compounds showed higher cytotoxic effects than Cisplatin. The DFT method was applied to determine the electronic structure characteristics of 1,4-naphthoquinone derivatives associated with cytotoxicity. A method of determination of 2,3-dichloro-1,4-naphthoquinone (NQ), 3-chloro-2-((4-hydroxyphenylamino)-1,4-naphthoquinone (NQ1), and 4-((3-chloro-1,4-naphthoquinon-2-yl)amino)phenyl fluorosulfate (NQS) in a pharmaceutical substance using an impregnated graphite electrode (IMGE) was developed. The morphology of the IMGE surface was studied using scanning electron microscopy (SEM). The electrochemical behavior of NQ, NQ1, and NQS was studied by cyclic voltammetry (CV) in 0.1 M NaClO4 (96% ethanol solution) at pH 4.0 in a potential range from −1 to +1.2 V. Electrochemical redox mechanisms for the investigated compounds were proposed based on the determining main features of the electrochemical processes. Calibration curves were obtained by linear scan voltammetry in the first derivative mode (LSVFD) with the detection limit (LOD) 7.2 × 10−6 mol·L−1 for NQ, 8 × 10−7 mol·L−1 for NQ1, and 8.6 × 10−8 mol·L−1 for NQS, respectively.

Reactive oxygen species (ROS) involving superoxide anion, hydrogen peroxide and hydroxyl radical play important role in human health. ROS are known to be the markers of oxidative stress associated with different pathologies including neurodegenerative and cardiovascular diseases, as well as cancer. Accordingly, ROS level detection in biological systems is an essential problem for biomedical and analytical research. Electrochemical methods seem to have promising prospects in ROS determination due to their high sensitivity, rapidity, and simple equipment. This review demonstrates application of modern electrochemical sensors for ROS detection in biological objects (e.g., cell lines and body fluids) over a decade between 2011 and 2021. Particular attention is paid to sensors materials and various types of modifiers for ROS selective detection. Moreover, the sensors comparative characteristics, their main advantages, disadvantages and their possibilities and limitations are discussed.

A method of determination of 2,3-dichloro-1,4-naphthoquinone (NQ), 2-chloro-3-((4-hydroxyphenylamino)-1,4-naphthoquinone (NQ1), and 4-((3-chloro-1,4-naphthoquinon-2-yl) amino)-phenyl sulfurofluoridate (NQS) in pharmaceutical preparations using impregnated graphite electrode (IMGE) was developed. The morphology of the IMGE surface was studied using scanning electron microscopy (SEM). The electrochemical behavior of NQ, NQ1, and NQS was studied by cyclic voltammetry (CV) in 0.1 М NaClO4 (96% ethanolic solution) pH 4.0 in a potential range from -1 to +1.2 V. Electrochemical redox mechanism for investigated substances was proposed. Calibration dependences of the analytical signal on the concentration of investigated analytes under optimal experimental conditions were obtained by the first-order derivative linear sweep voltammetry (FODLSV) with the limit of detection (LOD) 7.2·10-6 mol·l-1 for NQ, 8·10-7 mol·l-1 for NQ1, and 8.6·10-8 mol·l-1 for NQS, respectively.

Graphene (GR) composites have great potential for the determination of carbamates pesticides (CPs) by electrochemical methods. Since the beginning of the 20th century, GR has shown remarkable promise as electrode material for various sensors. The contamination of food products with harmful CPs is a major problem as they do not always damage human health immediately, but can be harmful after prolonged exposure. A range of advantages can be gained from their electrochemical determination, such as high sensitivity, reasonably selectivity, rapid detection, low limit of detection, and easy electrode fabrication. Furthermore, these electrochemical techniques are robust, reproducible, user-friendly, and conform to both "green" and "white" analytical chemistry. This review is focused on results published in the last ten years in the field of electrochemical determination of CPs in food products using GR and its derivatives.

The determination of carbofuran (CBF) in herbs (wild chamomile and Saint-John's-wort) was developed using a carbon-containing electrode (CCE) modified with carbon ink (CI) containing chromatographic sorbent (CS) based on chromaton (Ch), polyethylene glycol (PEG), and iron acetylacetonate (Fe(AA)(3)). The surface morphology of the Ch/PEG/Fe(AA)(3)/CI/CCE was investigated by scanning electron microscopy (SEM) in backscatteredelectron (BSE) mode and by electrochemical impedance spectroscopy (EIS). Electrochemically inactive CBF was converted to an electrochemically active phenolic analogue CBFP by an alkaline hydrolysis. The electrochemical behavior of CBFP at Ch/PEG/Fe(AA)(3)/CI/CCE was studied by cyclic voltammetry (CV) in a phosphate buffer solution (PBS) pH 6.86 in the potential range from -0.4 to 1.2 V. Under the optimal experimental conditions, linear concentration dependences in the concentration range from 0.25 to 10 mu mol center dot L-1 were obtained by linear scan voltammetry in the first derivative mode (LSVFD) with limit of detection (LOD) 0.08 mu mol center dot L-1. The proposed Ch/PEG/Fe(AA)(3)/CI/CCE demonstrated good sensitivity and selectivity for the determination of CBF after its conversion to CBFP. The use of sorbents as modifying agents of electrodes for the determination of carbamate pesticides opens up the possibilities for "green" electroanalytical chemistry.