A new electrochemical adsorptive stripping voltammetry method was developed for the determination of trace amounts of copper in food and water samples. The study of electrochemical behavior of Cu ion indicated that Cu(II) and Schiff base formed a complex in H3BO4-NaOH buffer solution (pH = 7.25). An accumulation potential of -100 mV (vs Ag/AgCl) was applied while the solution was stirred for 60 s. The response curve was recorded by scanning the potential, and the peak current of -0.31 V (vs Ag/AgCl) was recorded. The peak current and concentration of copper accorded with linear relationship in the range of 0.04-120 ng mL(-1). The relative standard deviation (for 12 ng mL(-1) of copper) was 1.73 %, and the detection limit was 0.007 ng mL(-1). The possible interference of some common ions was studied. The proposed method was applied to the determination of copper in water, rice, wheat, tea, milk, and tomato with satisfactory results.

Pharmaceutical and food pollutants have threatened global health. Pharmacotherapy has left a positive impression in the field of health and life of people and animals. However, the many unresolved problems brought along with residues of pharmaceuticals in the environmental and food. Consumption of the world's freshwater resources, toxic chemicals, air pollution, plastic waste directly affects water and soil resources. Pesticides have a wide role in pollutants. Therefore, the determination of pesticides is significant to eliminate their negative effects on living things. Nowadays, there are many analytical methods available. However, new analysis methods are still being researched due to certain limitations of traditional methods. Electrochemical sensors have drawn attention because of their superior properties, such as short analysis time, affordability, high sensitivity, and selectivity. The development of new analytical strategies for assessing risks from pharmaceutical to food pollutants in water and soil sources is important for the measurement of different pollutants. Moreover, the 2D-carbon nanomaterials used in the development of electrochemical sensors are widely utilized to enlarge the surface area, increase porosity, and make easy immobilization. Graphene (graphene derivations) and carbon nanotubes integrated nanosensors are widely used for the determination of pesticides. 2D-carbon nanomaterials can be tailored according to the purpose of the study. The characterization and synthesis methods of 2D-carbon nanomaterials are widely explained. Furthermore, enzyme nanobiosensors, especially Acetylcholinesterase (AChE), are widely used to determine pesticides. The three main topics are focused on in this review: 2D-carbon nanomaterials, pesticides that threaten life, and the application of 2D-carbon nanomaterials-based electrochemical sensors. The various developed 2D-carbon nanomaterials-based electrochemical sensors were applied in pharmaceutical forms, fruits, tap/lake water, beverages, and soils sources. This work aims to indicate the recently published paper related to pesticide analysis and highlight the importance of 2D-nanomaterials on sensors.

Emerging smartphone-based point-of-care tests (POCTs) are cost-effective, precise, and easy to implement in resource-limited areas. Thus, they are considered a potential alternative to conventional diagnostic testing. This review explores food safety and the detection of metal ions in environmental water based on unprecedented smartphone technology. Specifically, we provide an overview of various methods used for target analyte detection (antibiotics, enzymes, mycotoxins, pathogens, pesticides, small molecules, and metal ions), such as colorimetric, fluorescence, microscopic imaging, and electrochemical methods. This paper performs a comprehensive review of smartphone-based POCTs developed in the last three years (2018–2020) and evaluates their relative advantages and limitations. Moreover, we discuss the imperative role of new technology in the progress of POCTs. Sensor materials (metal nanoparticles, carbon dots, quantum dots, organic substrates, etc.) and detection techniques (paper-based, later flow assay, microfluidic platform, etc.) involved in POCTs based on smartphones, and the challenges faced by these techniques, are addressed.

The residues of antibiotics in the environment pose a potential health hazard, so highly sensitive detection of antibiotics has always appealed to analytical chemists. With the widespread use of new low-dimensional materials, graphene-modified electrochemical sensors have emerged as an excellent candidate for highly sensitive detection of antibiotics. Graphene, its derivatives and its composites have been used in this field of exploration in the last decade. In this review, we have not only described the field using traditional summaries, but also used bibliometrics to quantify the development of the field. The literature between 2011 and 2021 was included in the analysis. Also, the sensing performance and detection targets of different sensors were compared. We were able to trace not only the flow of research themes, but also the future areas of development. Graphene is a material that has a high potential to be used on a large scale in the preparation of electrochemical sensors. How to design a sensor with selectivity and low cost is the key to bring this material from the laboratory to practical applications.

Here we demonstrate a facile, two step formation of silver core - gold shell (Ag–Au) nanostructures using microelectrodes and assess their performance as surface-enhanced Raman scattering (SERS) substrates to detect and quantify toxicants. Ag nanostructures, serving as the scaffolds for the bimetallic structures, were grown first by using electrochemical deposition on the edges of microelectrodes functionalized with the alkanethiol, 11-mercaptoundecanoic acid. Subsequently, different concentrations of HAuCl₄ were used to perform a galvanic reaction on the surfaces of the Ag nanostructures with aqueous droplets being placed on the microelectrodes for 10 min before the substrate was rinsed and dried. Lower HAuCl₄ concentrations were found to better preserve the fractal morphology of the formed Ag–Au nanostructures, while higher concentrations resulted in Ag–Au fragments. The SERS enhancement factor for the Ag–Au nanostructures was estimated to have a max value of 6.51 x 10⁵. Combining a data reduction technique with a linear classifier, both identification and quantification were demonstrated with 100% success. The toxicants thiram, thiabendazole, malachite green and biphenyl-4-thiol were all detected and identified at 1 ppm. Lastly, as a proof of concept, the Ag–Au nanostructures were transferred to a PDMS film resulting in a flexible SERS substrate capable of direct detection of thiram on an apple peel without any additional sample pre-treatment.

Determination of selenium compounds in air, soil, water, and food samples is of interest as selenium's bioavailability and toxicity depend on its concentration level. Among analytical approaches, electrochemical sensors are more favorable due to their simplicity, time-saving, cost-effectiveness, and high sensitivity. In this study, we report electrochemical determination and analysis of selenium at the surface of a pencil graphite electrode modified with a sensing composite film composed of acetophenone (2,4-dinitrophenyl)hydrazone, polypyrrole, and copper nanoparticles. To produce durable films, cyclic voltammetry technique, as a facile modification procedure, was used. The electrochemical response of the fabricated modified electrode to selenium was evaluated using cyclic and square wave voltammetry techniques. The modified electrode presented excellent electrocatalytic ability with favorable electrochemical parameters (α = 0.24, log kₛ = 3.27 s⁻¹, and Γ = 3.74 × 10⁻⁷ mmol cm⁻²) for the reduction of selenium in acidic media with optimized pH of 2 and working potential of around −0.85 V (vs. SCE). The scanning electron microscopy images of the modified surfaces proved the formation of aggregates in nanoscale, indicating successful electrodeposition and electro-polymerization processes to modify the pencil graphite surface. This revealed a linear electrochemical response to selenium within the concentration range from 50 nM to 110 nM with the limit of detection (LOD) of 16.58 nM. The analytical application of the new sensor was also examined with respect to its applicability in food samples, such as milk, and water samples, including food wastewater samples, suggesting valid determination of selenium without any side interference.

This work presents, for the first time, a fast and highly sensitive electrochemical method for determination of three organophosphorus compounds (OPs), diazinon (DZN), malathion (MLT), and chlorpyrifos (CLPF), using a modified pyrolytic graphite electrode (PGE) coupled to batch injection analysis system with multiple pulse amperometric detection (BIA–MPA). The PGE was modified by a nanocomposite based on functionalized carbon nanotubes (CNTf) and silver nanoparticles (AgNPs). The OPs samples were directly analyzed on the modified working electrode surface by BIA-MPA system in Britton-Robinson (BR) buffer 0.15 mol L⁻¹ at pH 6.0. The MPA detection of DZN, MLT and CLPF was performed using two potential pulses, which were sequentially applied on modified PGE at −1.3 V (100 ms) and +0.8 V (100 ms) for selective determination of these three OPs and working electrode cleaning, respectively. Under optimized conditions, the sensor presented a linear range of 0.1–20 μmol L⁻¹ for DZN, 1.0–30 μmol L⁻¹ for MLT and from 0.25 to 50 μmol L⁻¹ for CLPF. The limits of detection (LOD) and quantification (LOQ) of 0.35 and 1.18 μmol L⁻¹ for DZN, 0.89 and 2.98 μmol L⁻¹ for MLT, and 0.53 and 1.78 μmol L⁻¹ for CLPF were obtained. The proposed method exhibited high sensitivity of 0.068, 0.030 and 0.043 mA L μmol⁻¹ for DZN, MLT and CLPF detection, respectively. Furthermore, the BIA-MPA system provided an analytical frequency of 71 determinations per hour for direct determination of these OPs in water and food samples. The modified PGE coupled to BIA-MPA system showed a high stability of electrochemical response for OPs detection with relative standard deviation (RSD) of 1.60% (n = 20). The addition-recovery studies of the proposed method were carried out in tap water, orange juice, and apple fruit real samples, which showed suitable recovery values between 77 and 124%. The analytical performance of the developed sensor provides an attractive alternative method for OPs determination with great potential for a fast and sensitive application in contaminated samples with these pesticides.