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Two analytical methods based on miniaturized electrochemical sensors, voltammetric and amperometric sensors, have been developed for the determination of 6-methyl-2-thiouracil (MTU) in meat consumption samples (beef liver and foie). A multivariate approach has been considered to optimize the experimental procedure including extraction and electrochemical detection. Under optimal conditions and at a typical working potential of 1.55 V (vs Ag pseudo-reference electrode), response is linear in the range 0 to 20 µg L−1 MTU concentration range. The empirical limit of detection is 0.13 µg L−1, lower than the maximum concentration established by legislation. The electrochemical methods have been used to analyze MTU-spiked meat samples, and recovery values varying between 85 and 95% with coefficients of variation <30%. The analytical methods developed with the miniaturized electrochemical sensors can successfully determine the concentration of MTU in real meat samples with high accuracy, being the results obtained similar to those provided by other methods such as UV-Vis spectrophotometry. Finally, the degree of sustainability of the electrochemical sensors-based developed method has been quantified by means of the Analytical Eco-Scale. [ABSTRACT FROM AUTHOR]

Soil tests for plant-available phosphorus (P) are suggested to provide offsite P analysis required to monitor P fertilizer application and reduce P losses to downstream water. However, procedural and cost limitations of current soil phosphate tests have restricted their widespread use and have made them accessible only in laboratories. This study proposes a novel paper-based reagentless electrochemical soil phosphate sensor to extract and detect soil phosphate using an inexpensive and simple approach. In this test, concentrated Mehlich-3 and molybdate ions were impregnated in filter paper, which served as the phosphate extraction and reaction zone, and was followed by electrochemical detection using cyclic voltammetry signals. Soil samples from 22 sampling sites were used to validate this method against inductively coupled plasma optical emission spectroscopy (ICP) soil phosphate tests. Regression and correlation analyses showed a significant relationship between phosphate determinations by ICP and the proposed method, delivering a correlation coefficient, r, of 0.98 and a correlation slope of 1.02. The proposed approach provided a fast, portable, low-cost, accessible, reliable, and single-step test to extract and detect phosphate simultaneously with minimum waste (0.5 mL per sample), which made phosphate characterization possible in the field. [ABSTRACT FROM AUTHOR]

A facile and rapid strategy to generate polypyrrole microcapsules is reported. The strategy is compatible with a vortex mixer and with a microfluidic chip for droplet generation, allowing a > 100-fold reduction in particle size. The sub-micron particle sizes obtained can also be tuned to some extent based on the chip geometry. The capsules can be kept stably in solution and can be transferred onto electrochemical devices. As an application example, we casted the polypyrrole capsules generated onto screen-printed electrodes, leading to a significant increase in their electroactive surface area and capacitance. The electrodes were further modified with glucose dehydrogenase (GDH) to fabricate glucose biosensors. The introduction of polypyrrole microcapsules increased the dynamic range of the glucose sensor to ca. 300% compared with that of the electrode without polypyrrole microcapsules. The resulting glucose sensor is operated at a constant applied potential of 0.20 V vs. Ag/AgCl (3 M KCl) in an air-equilibrated electrolyte. At this potential, the sensor showed a linear range from 1.0 to 9.0 mM glucose with a sensitivity of 3.23 µA cm−2 mM−1 (R2 = 0.993). The limit of detection obtained was 0.09 mM, and the reproducibility was 3.6%. The method allows generating polypyrrole microcapsules without surfactants or organic solvents and may enable new opportunities in the design of biosensors, electronic devices, and molecular delivery. [ABSTRACT FROM AUTHOR]

Electrochemical approaches, along with miniaturization of electrodes, are increasingly being employed to detect and quantify nucleic acid biomarkers. Miniaturization of the electrodes is achieved through the use of screen-printed electrodes (SPEs), which consist of one to a few dozen sets of electrodes, or by utilizing printed circuit boards. Electrode materials used in SPEs include glassy carbon (Chiang H-C, Wang Y, Zhang Q, Levon K, Biosensors (Basel) 9:2-11, 2019), platinum, carbon, and graphene (Cheng FF, He TT, Miao HT, Shi JJ, Jiang LP, Zhu JJ, ACS Appl Mater Interfaces 7:2979-2985, 2015). There are numerous modifications to the electrode surfaces as well (Cheng FF, He TT, Miao HT, Shi JJ, Jiang LP, Zhu JJ, ACS Appl Mater Interfaces 7:2979-2985, 2015). These approaches offer distinct advantages, primarily due to their demonstrated superior limit of detection without amplification. Using the SPEs and potentiostats, we can detect cells, proteins, DNA, and RNA concentrations in the nanomolar (nM) to attomolar (aM) range. The focus of this chapter is to describe the basic approach adopted for the use of SPEs for nucleic acid measurement., (© 2025. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.)

Screen-printed electrodes (SPEs) are promising candidates for fabricating biosensing platforms in the laboratory and industry due to the various advantages they involve. The primary method for fabricating SPEs is 2D printing. However, commercial SPEs have some limitations due to the specific ports and connections they require, inflexible design, high prices, and decreased efficiency after a short time. This article introduces high performance, feasible, and cost-effective gold SPEs based on the combination of printed circuit board substrate (PCBs) and sputtering methods for electrochemical biosensing platforms. First, we discuss a general gold SPE development procedure that helps researchers to develop specific designs. The final developed version of SPEs was characterized in the second step, showing positive performance in electrochemical parameters because of the optimization of design and fabrication steps. In the study’s final phase, SPEs were used to fabricate a simple platform for breast cancer cell detection as a proof of concept without using any linker or labeling step. The designed immunosensor is very simple and cost-effective, showing a linear calibration curve in the range of 10 − 2× 102 cells mL−1 (R2 = 0.985, S/N = 3). This research can be used as a reference for future studies in SPEs-based biosensors because of the flexibility of its design and the accessibility of the manufacturing equipment required.

This paper proposes a deep leaning technique for accurate detection and reliable classification of organic pollutants in water. The pollutants are detected by means of cyclic voltammetry characterizations made by using low-cost disposable screen-printed electrodes. The paper demonstrates the possibility of strongly improving the detection of such platforms by modifying them with nanomaterials. The classification is addressed by using a deep learning approach with convolutional neural networks. To this end, the results of the voltammetry analysis are transformed into equivalent RGB images by means of Gramian angular field transformations. The proposed technique is applied to the detection and classification of hydroquinone and benzoquinone, which are particularly challenging since these two pollutants have a similar electroactivity and thus the voltammetry curves exhibit overlapping peaks. The modification of electrodes by carbon nanotubes improves the sensitivity of a factor of about ×25, whereas the convolution neural network after Gramian transformation correctly classifies 100% of the experiments. [ABSTRACT FROM AUTHOR]

Electrochemical reforming of alkaline ethanol through nonfossil fuel resources is an attractive single‐step method at room temperature and pressure for hydrogen production. Herein, solar panels are used to generate and allow low‐voltage current to flow into screen‐printed electrodes with milliscale spacing to produce a high‐intensity electric field, engendering electrolysis of alkaline ethanol into H2. The introduction of gold nanoparticles (Au NPs) with diameters between 20 and 100 nm into the electrolyte results in an enhanced capacity of the electrolyzer to produce H2 under an illumination equivalent to solar irradiance. The plasmonic Au NPs facilitate faster electro‐oxidation of the alkaline ethanol. The solar irradiance serves dual purposes—generation of a high‐intensity electric field in the electrolyte and plasmonic effects for a faster rate of H2 production. The results show current densities as high as 135, 240, and 118 A m−2 with independent variations in sizes of Au NPs, wavelength of solar radiation, and irradiance of light, respectively. Furthermore, a high Faradaic efficiency of 82% is obtained for the electrolyte solution containing Au NPs of size 50 nm. Integration of multiple screen‐printed electrodes shows further enhancement of H2 throughput, leaving a niche for the prototype to scale‐up H2 production. [ABSTRACT FROM AUTHOR]

Human Papilloma Virus 16 (HPV 16) is the well-known causative species responsible for triggering cervical cancer. When left undiagnosed and untreated, this disease leads to life-threatening events among the female populace, especially in developing nations where healthcare resources are already being stretched to their limits. Considering various drawbacks of conventional techniques for diagnosing this highly malignant cancer, it becomes imperative to develop miniaturized biosensing platforms which can aid in early detection of cervical cancer for enhanced patient outcomes. The current study reports on the development of an electrochemical biosensor based on reduced graphene oxide (rGO)/DNA hybrid modified flexible carbon screen-printed electrode (CSPE) for the detection of HPV 16. The carbon-coated SPEs were initially coated with rGO followed by probe DNA (PDNA) immobilization. The nanostructure characterization was performed using UV-Vis spectroscopy, Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy and X-ray diffraction (XRD) techniques. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were employed to study the electrochemical characterization of the nano-biohybrid sensor surface. The optimization studies and analytical performance were assessed using differential pulse voltammetry (DPV), eventually exhibiting a limit of detection (LoD) ~2 pM. The developed sensor was found to be selective solely to HPV 16 target DNA and exhibited a shelf life of 1 month. The performance of the developed flexible sensor further exhibited a promising response in spiked serum samples, which validates its application in future point-of-care scenarios. [ABSTRACT FROM AUTHOR]

The identification of the reaction product species stands out as one of the main limitations of the classical electrochemical techniques. This can be overcome by the combination of electrochemistry (EC) to mass spectrometry (MS). Moreover, the method can be further enhanced by implementing a separation technique between EC and MS. In the present work, the oxidation behavior of cysteine with coupling EC directly to MS (real-time EC–MS) or by implementing capillary electrophoresis (CE), to separate the analytes before the injection into the mass spectrometer, is investigated. Electrochemical measurements and pre-treatment were applied on screen-printed electrodes (SPEs) based on carbon. Direct EC–MS measurements were carried out with a modified flow cell, while online EC–CE–MS studies of cysteine oxidation were conducted with a custom-made setup. An electrochemical conversion yield for cysteine of up to 69% was found. Cystine, cysteic acid, and cysteine sulfinic acid were found as oxidation products. The identification of these product species was carried out according to their migration behavior in CE, and mass-to-charge ratios in addition to their isotopic patterns shown in the MS spectra. [ABSTRACT FROM AUTHOR]

In this work, we have investigated the electrochemical properties of 4′-hydroxydiclofenac, which is the main product of cytochrome P450 2C9 (CYP2C9)-dependent metabolism of a nonsteroidal anti-inflammatory drug — diclofenac. Cyclic voltammogram of 4′-hydroxydiclofenac registered in 100 mM potassium phosphate buffer (pH 7.4) containing 50 mM NaCl and 1% methanol on unmodified screen-printed electrodes (SPE) is characterized by an oxidation peak at 0.297 ± 0.012 V (vs. Ag/AgCl) and a reduction peak at −0.308 ± 0.018 V (vs. Ag/AgCl), while the oxidation peaks of diclofenac are found to be at 0.587 ± 0.013 V (vs. Ag/AgCl) and 0.992 ± 0.015 V (vs. Ag/AgCl). Based on differences in electrochemical behavior of diclofenac and 4′-hydroxydiclofenac, we proposed an approach to CYP2C9 activity analysis by quantitative electrochemical determination of the metabolite. To increase the sensitivity and decrease the limit of detection of the 4′-hydroxydiclofenac determination, we modified the SPE by single-wall carbon nanotubes (SWCNT) water dispersion TUBALL™ BATT H2O. Using square-wave voltammetry, we obtained dependence of the oxidation peak current on 4′-hydroxydiclofenac concentration in the potassium phosphate buffer. The sensitivity and the limit of detection were calculated to be 0.11 μA/μM and 0.085 μM, respectively. We applied the electrochemical method of 4′-hydroxydiclofenac determination to analyze the catalytic activity of CYP2C9 immobilized on SPE modified by didodecyldimethylammonium bromide (DDAB). The values of the maximum rate of enzymatic 4′-hydroxylation of diclofenac in the electrochemical system (Vmax) and the Michaelis constant (KM) were determined as 5.35 ± 0.13 min−1 and 11.66 ± 0.92 μM, respectively. Using a known competitive inhibitor of CYP2C9 sulfaphenazole, we showed the applicability of the developed approach based on the electrochemical determination of 4′-hydroxydiclofenac for inhibitor analysis, which is essential for pharmacological research. [ABSTRACT FROM AUTHOR]

The present work reports the development of screen-printed electrode (SPE) using flexible polyester sheets modified with nanodiamond (ND), Au nanoparticles (AuNPs), and poly(3,4-ethylene dioxythiophene):polystyrene sulfonate (PEDOT:PSS), and its application for the detection of tryptophan in synthetic urine, milk, and dark chocolate samples. The ND/AuNPs/PEDOT:PSS nanocomposite was characterized by cyclic voltammetry, scanning electron microscopy and energy-dispersive X-ray spectroscopy. The proposed ND/AuNPs/PEDOT:PSS-based SPE was applied for the detection of tryptophan using square-wave voltammetry in a linear detection range of 0.8 µmol L−1–18 µmol L−1, with limits of detection (LOD) and quantification (LOQ) of 0.2 µmol L−1 and 0.8 µmol L−1, respectively. The sensor was successfully applied for tryptophan quantification in dark chocolate, milk and synthetic urine where good recovery percentages were obtained. The results obtained from the analysis of interference in the presence of dopamine and caffeine showed that the ND/AuNPs/PEDOT:PSS-based SPE exhibited excellent selectivity toward tryptophan. The findings of this study show that metallic nanoparticles, nanodiamonds and biocompatible conductive composites can be used as a suitable, affordable alternative tool for fast, simple, and low-cost detection of tryptophan in non-invasive testing and analysis of food products. [ABSTRACT FROM AUTHOR]

Monitoring the concentration of antibiotics in body fluids is essential to optimizing the therapy and minimizing the risk of bacteria resistance, which can be made with electrochemical sensors tailored with appropriate materials. In this paper, we report on sensors made with screen-printed electrodes (SPE) coated with fullerene (C60), reduced graphene oxide (rGO) and Nafion (NF) (C60-rGO-NF/SPE) to determine the antibiotic metronidazole (MTZ). Under optimized conditions, the C60-rGO-NF/SPE sensor exhibited a linear response in square wave voltammetry for MTZ concentrations from 2.5 × 10−7 to 34 × 10−6 mol/L, with a detection limit of 2.1 × 10−7 mol/L. This sensor was also capable of detecting MTZ in serum and urine, with recovery between 94% and 100%, which are similar to those of the standard chromatographic method (HPLC-UV). Because the C60-rGO-NF/SPE sensor is amenable to mass production and allows for MTZ determination with simple principles of detection, it fulfills the requirements of therapeutic drug monitoring programs.

Accurate determination of dopamine (DA) and uric acid (UA) in biological samples is crucial in diagnosing neurodegenerative disorders and gout, respectively. Here we report a highly sensitive and inexpensive, flexible screen-printed sensor for determining DA and UA in sweat samples. Beta-cyclodextrin-based (βCD) composite gel with reduced graphene oxide (rGO) was synthesized by self-polymerization of βCD at an optimum ratio of "good" and "poor solvent". Multiwall carbon nanotubes (MWCNTs) were incorporated into the composite as a conductive filler. The MWCNTs-βCD-rGO gel provides selective biorecognition of DA and UA at the electrode surface through guest-host interaction. The gels were characterized by XRD, TGA, FTIR, UV–Vis, 1H NMR, FESEM, XPS and optical microscopy. The flexible printed sensor showed linear DA detection in the range 0.25 to 16 μM with a correlation coefficient (R2) of 0.9890, limit of detection (LoD) of 0.08 μM and sensitivity of 3.63 μA μM−1 cm−2. Similarly, UA calibration showed linear detection from 50 to 700 μM with a R2 value of 0.9860, LoD of 0.078 μM and sensitivity of 0.118 μA μM−1 cm−2. The SPE/MWCNTs-βCD-rGOsensor showed simultaneous determination of DA and UA from exercise induced sweat samples. The proposed sensor demonstrated excellent repeatability and satisfactory recoveries in human sweat. [Display omitted] [ABSTRACT FROM AUTHOR]

Coeliac disease is a very common autoimmune disease estimated to affect 1 in 100 people worldwide. It occurs in genetically predisposed people where the ingestion of gluten leads to damage in the small intestine, and it is accurately diagnosticated through duodenal biopsy, an invasive diagnostic method. The liquid biopsy, generally used for monitoring cancer, is an appealing alternative even for autoimmune pathology such as coeliac disease, allowing for detecting disease progression or resistance to treatment. For this reason, an electrochemical peptide nucleic acid (PNA) device combined with a smartphone‐assisted potentiostat for non‐invasive coeliac disease diagnosis is proposed, by measuring the selected overexpressed miRNA‐486‐5p in serum, enlarging the application of liquid biopsy in nontumor pathologies. For highly sensitive detection, the polyester‐based printed sensor is nanomodified with gold nanoparticles and a synthetic customized PNA probe. The designed sensor can detect the target analyte in the range of 10–100 nm with a limit of detection of 0.7 nm by measuring the variation of the response of the electrochemical mediator hexaammineruthenium in the presence of PNA–miRNA duplex on the nanostructured working electrode surface. The analyses testing serum samples are found in agreement with ones obtained by real‐time quantitative polymerase chain reaction (RT‐qPCR), demonstrating the reliability of this innovative electrochemical chip developed.

Abstract The indiscriminate use of herbicides in agriculture contributes to soil and water pollution, with important endangering consequences on the ecosystems. Among the available analytical systems, algal biosensors have demonstrated to be valid tools thanks to their high sensitivity, cost-effectiveness, and eco-design. Herein, we report the development of a dual electro-optical biosensor for herbicide monitoring, based on Chlamydomonas reinhardtii whole cells immobilised on paper-based screen-printed electrodes modified with carbon black nanomaterials. To this aim, a systematic study was performed for the selection and characterisation of a collection among 28 different genetic variants of the alga with difference response behaviour towards diverse herbicide classes. Thus, CC125 strain was exploited as case study for the study of the analytical parameters. The biosensor was tested in standard solutions and real samples, providing high sensitivity (detection limit in the pico/nanomolar), high repeatability (RSD of 5% with n = 100), long lasting working (10 h) and storage stability (3 weeks), any interference in the presence of heavy metals and insecticides, and low matrix effect in drinking water and moderate effect in surface one.

This paper presents the development of a cheap and rapid electrochemical sensor for ascorbic acid detection. In particular, the graphite ink working electrode of screen-printed cells was covered by a film of elecrosynthesized molecularly imprinted polypyrrole (e-MIP); differential pulse voltammetry (DPV) was the selected method for the analyte detection. The ascorbic acid molecules were successfully entrapped in the polypyrrole film, creating the recognition sites. The best results were obtained after polypyrrole overoxidation and performing the measurements in phosphate buffer solution 0.05 M/KCl 0.1 M at pH 7.5. A comparison with the bare and the not-imprinted polypyrrole-modified electrodes showed that the e-MIP-based sensor had the highest selectivity and reproducibility. The developed method was applied to assess ascorbic acid in farmaceutical products, obtaining values not significantly different from the declared content.

[Display omitted] • Enhancing Electroanalytical Performance: Selecting Optimal Carbon Inks for Screen-Printed Electrodes. • Characterization revealed differences in (electro)chemical properties of electrodes. • The critical role of selecting suitable inks for diverse electroanalytical analyses. • Variations in ink formulation led to differences in the sensing abilities. • Enhanced selective reductive sensing due to an ion-exchange polymer layer. Carbon-based screen-printed electrodes (SPEs) are extensively employed in electrochemistry due to their reproducibility, low-cost production, disposability and versatility. It is commonly accepted that batch to batch variations may occur due to variations in the ink formulation or the use of a different ink to print the electrodes. In this paper, three different commercial carbon-based inks (DuPont, Loctite and SunChemical) were used to manufacture SPEs, referred to respectively as Dup-SPE, Loc-SPE and Sun-SPE, using a semi-automated screen-printing technology. This study focuses on evaluating the quality, characteristics and electrochemical performance of the fabricated SPEs. Furthermore, the study aimed to investigate potential correlations between the ink composition and the nature of different target molecules, as well as their electroanalytical responses. Specifically, phenolic compounds and cocaine cutting agents are tested in alkaline conditions, while benzodiazepines and cephalosporine antibiotics are investigated in acidic media using square wave voltammetry (SWV). This aims to extract insights for the proper selection of inks and SPEs in both conditions. Additionally, a scan rate study of cephalosporine antibiotics using linear sweep voltammetry (LSV) is performed confirming the ion-exchange polymer layer on the electrode surface of Loc-SPE, which impact surface and electrochemical properties, leading to drawbacks in alkaline SWV sensing, but strategic benefits in reductive sensing resulting in an enhanced selective detection of specific targets. The insights on ink-specific influences on the surface and electrochemical properties of the SPEs obtained, may be useful for facilitating the electrode selection in diverse electrochemical applications, emphasizing the critical role of ink composition in achieving desired sensing capabilities. [ABSTRACT FROM AUTHOR]

The availability of new surface enhanced Raman scattering (SERS) substrates is essential to develop quantitative analytical methods. Electrochemistry is an easy, fast and reproducible methodology to prepare SERS substrates on screen-printed electrodes (SPEs). This work proposes new SPEs based on a three-electrode system all made of silver. Using the same ink for the whole electrode system facilitates the fabrication process, reduces production costs, and leads to excellent analytical performance. The results showed that Raman enhancement depends strongly on the type of silver ink. To demonstrate the capabilities of the new electrodes developed, 4-aminosalicylic acid was determined in complex matrices and in the presence of strong interfering compounds such as salicylic acid and acetylsalicylic acid. The proposed analytical method is based on the electrochemical surface oxidation enhanced Raman scattering (EC-SOERS) strategy. AgCl nanocrystals are generated on the working electrode surface, which amplify the Raman signal of 4-aminosalicylic acid. Good figures of merit were obtained both in the absence and in the presence of the interfering compounds, achieving a correct estimation of a 4-aminosalicylic test sample in complex matrices. The new SPEs have been demonstrated to be very sensitive and reproducible which, together to the high specificity of the Raman signal, makes this methodology very attractive for chemical analysis. [Display omitted] • New screen-printed electrodes for EC-SOERS analysis. • Three electrode system based on silver. • Raman enhancement depends on the type of silver ink. • Determination of 4-aminosalicylic acid in complex matrices. [ABSTRACT FROM AUTHOR]

Glassy carbon (GC) electrodes are crucial in electrochemistry due to their chemical stability and excellent electrochemical behaviour. This study presents the development of screen-printed glassy electrodes and demonstrates their suitability for electrogenerated electrochemiluminescence (ECL) applications. Model ECL system tris (2,2′-bipyridyl) ruthenium (II)/tripropylamine (Ru(bpy) 3 2+/TPA) is used to benchmark the new electrodes. Different ink formulations are presented, and the electrochemical performance of the corresponding printed electrodes is discussed. In contrast to graphite screen printed electrodes, laser activation did not result in significant benefits at these new GC electrodes. A range of characterization techniques such as scanning electron microscopy, Raman spectroscopy, and spectroelectrochemical methods are used in the study. ECL studies of the GC electrodes was studied using both UV–Vis spectroscopy and image analysis. An ink formulation consisting of a GC to binder ratio of 5:1 by weight yielded the best results, surpassing the response of commercial graphite screen-printed electrodes, and in line with conventional (bulk) glassy carbon electrodes. [ABSTRACT FROM AUTHOR]

We introduce a bifunctional architecture to construct biosensors on solution-blow spinning fiber mats of polylactic acid (PLA) and polyethylene glycol (PEG). PLA/PEG mats acted as substrate for printing electrodes and as matrix to immobilize glucose oxidase (GOx). Prussian Blue nanoparticles (PB) decorated working electrodes to detect H2O2 from enzymatic catalysis at a low applied potential (0 V vs. Ag/AgCl) with detection limit of 0.197 mM. The inexpensive bifunctional device (

A novel cost-effective disposable porous graphene electrode (P-GE) modified with bismuth nanoneedles (nano-BiNDs) is proposed as a "mercury-free" sensor for detecting heavy metals through smartphone-assisted electrochemical sensing. The P-GE was fabricated using screen-printing. Nano-BiNDs were generated on the P-GE by potentiostatic electrodeposition. Using an optimal potential of −1.20 V (vs. pseudo-Ag/AgCl) and a deposition time of 200 s, the nano-BiNDs had an average length and width of 189 ± 5 nm and 20 ± 2 nm, respectively. The analytical performances of the fabricated sensing platform were demonstrated by detecting Cd2+ and Pb2+ using square-wave anodic stripping voltammetry (SWASV) under optimized conditions. In the optimal conditions, the fabricated sensor exhibited sharp, well-defined stripping peaks for Cd2+ and Pb2+ with excellent peak-to-peak separation. The linear detection ranges were from 0.01 to 50 μg mL−1 for Cd2+ and 0.006–50 μg mL−1 for Pb2+. The detection limits for Cd2+ and Pb2+ were 3.51 and 2.10 ng mL−1, respectively. The developed portable sensor demonstrated high sensitivity, good repeatability, reproducibility, and anti-interference properties. The proposed portable sensor quantified Cd2+ and Pb2+ in commercial seaweed products with good accuracy, consistent with the results obtained using the standard ICP-OES method. [Display omitted] • A flexible disposable porous graphene electrode (P-GE) was fabricated by screen printing. • The electrode was modified with nano-BiNDs by potentiostatic electrodeposition. • The electrode was used in a smartphone-assisted portable sensor for Cd2+ and Pb2+. • The sensor exhibited good performances for Cd2+ and Pb2+ determination by SWASV. • The sensor detected Cd2+ and Pb2+ in seaweed products. [ABSTRACT FROM AUTHOR]

Deferoxamine (DFO), a hydroxamic siderophore with a high affinity for Fe(III), is immobilized as a functionalized self-assembled monolayer of a thiol (SAM) on the gold surface of a screen-printed cell to develop a voltammetric sensor for iron(III). The surface of the working electrode was characterized, before and after functionalization, by determining surface properties such as the area and the double-layer capacitance. The Fe(III) detection was performed by DPV analysis after preconcentration of the cation at the open circuit potential in solution at pH = 1 for two minutes. The method was applied to the iron(III) quantification in water samples giving promising results. [ABSTRACT FROM AUTHOR]

Herein, we report a proof-of-concept algal cytosensor for the electrochemical quantification of bacteria in wastewater, exploiting the green photosynthetic alga Chlamydomonas reinhardtii immobilized on carbon black (CB) nanomodified screen-printed electrodes. The CB nanoparticles are used as nanomodifiers, as they are able to sense the oxygen produced by the algae and thus the current increases when algae are exposed to increasing concentrations of bacteria. The sensor was tested on both standard solutions and real wastewater samples for the detection Escherichia coli in a linear range of response from 100 to 2000 CFU/100 mL, showing a limit of detection of 92 CFU/100 mL, in agreement with the maximum E. coli concentration established by the Italian law for wastewater (less than 5000 CFU/100 mL). This bacterium was exploited as a case study target of the algal cytosensor to demonstrate its ability as an early warning analytical system to signal heavy loads of pathogens in waters leaving the wastewater treatment plants. Indeed, the cytosensor is not selective towards E. coli but it is capable of sensing all the bacteria that induce the algae oxygen evolution by exploiting the effect of their interaction. Other known toxicants, commonly present in wastewater, were also analyzed to test the cytosensor selectivity, with any significant effect, apart from atrazine, which is a specific target of the D1 protein of the Chlamydomonas photosystem II. However, the latter can also be detected by chlorophyll fluorescence simultaneously to the amperometric measurements. The matrix effect was evaluated, and the recovery values were calculated as 105 ± 8, 83 ± 7, and 88 ± 7% for 1000 CFU/100 mL of E. coli in Lignano, San Giorgio, and Pescara wastewater samples, respectively. [ABSTRACT FROM AUTHOR]

Water pollution is nowadays a global problem and the effective detection of pollutants is of fundamental importance. Herein, a facile, efficient, robust, and rapid (response time < 2 min) method for the determination of important quinone-based industrial pollutants such as hydroquinone and benzoquinone is reported. The recognition method is based on the use of screen-printed electrodes as sensing platforms, enhanced with carbon-based nanomaterials. The enhancement is achieved by modifying the working electrode of such platforms through highly sensitive membranes made of Single- or Multi-Walled Carbon Nanotubes (SWNTs and MWNTs) or by graphene nanoplatelets. The modified sensing platforms are first carefully morphologically and electrochemically characterized, whereupon they are tested in the detection of different pollutants (i.e., hydroquinone and benzoquinone) in water solution, by using both cyclic and square-wave voltammetry. In particular, the sensors based on film-deposited nanomaterials show good sensitivity with a limit of detection in the nanomolar range (0.04 and 0.07 μM for SWNT- and MWNT-modified SPEs, respectively) and a linear working range of 10 to 1000 ppb under optimal conditions. The results highlight the improved performance of these novel sensing platforms and the large-scale applicability of this method for other analytes (i.e., toxins, pollutants). [ABSTRACT FROM AUTHOR]

Detection of stress biomarkers molecules, non-invasively, through (non-induced) sweat sampling is an important research field since sweat is a potential diagnostic fluid for early and continuous human health monitoring, not only for stress-related conditions directly but also for other pathologies (e.g., associated with chronic diseases). The simultaneous detection of multiple potential biomarkers in sweat samples, using simple and low-cost electrochemical methods (detecting patterns or "electrochemical fingerprints") requiring no sample preparation and its correlation with physiological conditions, is an attractive methodology but not readily achievable. Several of these potential biomarkers' electrochemical response presents very close oxidation potentials, among other factors that hamper the detection, such as pH dependence of the electrochemical response or partial adsorption on electrode surfaces. Disposable screen-printed electrode materials, with relatively low-cost, could be useful to overcome the difficulties. A set of selected potential stress-related (non-protein) biomarkers (tyrosine, phenylalanine, dopamine, serotonin, and hydrocortisone) was used in the current study for qualitative electrochemical detection on different screen-printed carbon-based electrodes. The detection was attained in simulated sweat solutions and real sweat samples. The goal was to evaluate the electrochemical response on the different surfaces and determine the most suitable carbon-based screen-printed electrodes that may be used in future sensing devices. [ABSTRACT FROM AUTHOR]

The rapid spread of the novel human coronavirus 2019 (COVID-19) and its morbidity have created an urgent need for rapid and sensitive diagnostics. The real-time polymerase chain reaction is the gold standard for detecting the coronavirus in various types of biological specimens. However, this technique is time consuming, labor intensive, and expensive. Screen-printed electrodes (SPEs) can be used as point-of-care devices because of their low cost, sensitivity, selectivity, and ability to be miniaturized. The ability to detect the spike protein of COVID-19 in serum, urine, and saliva was developed using SPE aided by magnetic beads (MBs) and a portable potentiostat. The antibody-peroxidase-loaded MBs were the captured and catalytic units for the electrochemical assays. The MBs enable simple washing and homogenous deposition on the working electrode using a magnet. The assembly of the immunological MBs and the electrochemical system increases the measuring sensitivity and speed. The physical and electrochemical properties of the layer-by-layer modified MBs were systematically characterized. The performance of these immunosensors was evaluated using spike protein in the range 3.12–200 ng mL−1. We achieved a limit of detection of 0.20, 0.31, and 0.54 ng mL−1 in human saliva, urine, and serum, respectively. A facile electrochemical method to detect COVID-19 spike protein was developed for quick point-of-care testing. [ABSTRACT FROM AUTHOR]

Screen-printed electrodes-based sensors can be successfully used to determine all kinds of analytes with great precision and specificity. However, obtaining a high-quality sensor can be difficult due to factors such as lack of reproducibility, surface contamination or other manufacturing challenges. An important step in ensuring reproducible results is the cleaning step. The aim of the current work is to help researchers around the world who struggle with finding the most suitable method for cleaning screen-printed electrodes. We evaluated the cleaning efficiency of different chemical compounds and cleaning methods using cyclic voltammetry and electrochemical impedance spectroscopy. The percentage differences in polarization resistance (Rp) before and after cleaning were as follows: acetone—35.33% for gold and 49.94 for platinum; ethanol—44.50% for gold and 81.68% for platinum; H2O2—47.34% for gold and 92.78% for platinum; electrochemical method—3.70% for gold and 67.96% for platinum. Thus, we concluded that all the evaluated cleaning methods seem to improve the surface of both gold and platinum electrodes; however, the most important reduction in the polarization resistance (Rp) was obtained after treating them with a solution of H2O2 and multiple CV cycles with a low scanning speed (10 mV/s). [ABSTRACT FROM AUTHOR]

As one of the three major chronic diseases, diabetes often causes many complications, which can affect various parts of the body and even threaten the life of the patients. At present, the situation of diabetes in the world is quite serious. Accurate detection of blood glucose is very important for the diagnosis, treatment and medication of diabetes as well as the self-management of diabetic patients. In this paper, an electrochemical glucose biosensor was developed based on screen-printed electrode (SPE) modified with composite material of graphene aerogel (GA) and Prussian blue (PB) (denoted as GA@PB), which was fabricated via chemical reduction using L-ascorbic acid as a reducing agent through a freeze-drying process. Glucose was specifically captured by glucose oxidase (GOx) which were immobilized into the GA@PB by chitosan. The structure and performance of the sensor were characterized by scanning electron microscopy (SEM), Raman spectroscopy measurements, Fourier transform infrared spectrometer (FTIR), cyclic voltammetry (CV) and amperometric detection. The sensor exhibited a linear range of 0.5–6.0 mmol·L−1 with limit of detection (LOD) of 0.15 mmol·L−1, indicating that the combination of graphene aerogel and Prussian blue possess well conductivity and catalytic performance. [ABSTRACT FROM AUTHOR]

Polythionine (PTH) is an electroactive compound known for its excellent electron transfer capacity. It has stable and redox centers in its structure, and it can also be generated by electropolymerization of thionine (TH). Due to its properties, it has been used in a large number of applications, including the construction of electrochemical biosensors. In this work, PTH is explored for its ability to generate electrons, which allows it to act as an electrochemical probe in a biosensor that detects CA 19-9 on two different substrates, carbon and gold, using differential pulse voltammetry (DPV) as a reading technique in phosphate buffer (PhB). The analytical features of the resulting electrodes are given, showing linear ranges from 0.010 to 10 U/mL. The Raman spectra of PTH films on gold (substrates or nanostars) and carbon (substrates) are also presented and discussed as a potential use for SERS readings as complementary information to electrochemical data. [ABSTRACT FROM AUTHOR]

A simple, fast, sensitive and low-cost voltammetric method using a screen-printed carbon electrode (SPCE) is presented in this work for the simultaneous determination of ascorbic acid (AA), paracetamol (PA), dextromethorphan (DX) and caffeine (CF) in both pharmaceutical formulations and samples of environmental interest. The oxidative peak current displayed linear dependence on concentration within the range 1.7–60.5, 0.6–40.0, 0.9–8.4 (1st linear part) and 1.8–22.0 mg L−1 for AA, PA, DX and CF, respectively; and detection limits of 0.5, 0.2, 0.3 and 0.5 mg L−1, respectively. The developed differential pulse voltammetric (DPV) method was validated using both a pharmaceutical product and a spiked well water sample. A very good agreement between the determined and the theoretical label drug content and recoveries in the range of 99.5–100.8% were obtained for pharmaceutical product and well water samples, respectively. [ABSTRACT FROM AUTHOR]

The smuggling of illicit drugs urges the development of new tools for rapid on-site identification in cargos. Current methods rely on presumptive color tests and portable spectroscopic techniques. However, these methods sometimes exhibit inaccurate results due to commonly used cutting agents, the colorful nature of the sample or because the drugs are smuggled in common goods. Interestingly, electrochemical sensors can deal with these specific problems. Herein, an electrochemical device is presented that uses affordable screen-printed electrodes for the electrochemical profiling of several illicit drugs by square-wave voltammetry (SWV). The identification of the illicit compound is based on the oxidation potential of the analyte. Hence, a library of electrochemical profiles is built upon the analysis of illicit drugs and common cutting agents. This library allows the design of a tailor-made script that enables the identification of each drug through a user-friendly interface (laptop or mobile phone). Importantly, the electrochemical test is compared by analyzing 48 confiscated samples with other portable devices based on Raman and FTIR spectroscopy as well as a laboratory standard method (i.e., gas chromatography–mass spectrometry). Overall, the electrochemical results, obtained through the analysis of different samples from confiscated cargos at an end-user site, present a promising alternative to current methods, offering low-cost and rapid testing in the field. [ABSTRACT FROM AUTHOR]

This review is presenting the design and performance of some electrochemical sensors used for the determination of L-dopa in real samples as reported in a series of relevant scientific papers published in the past 5 years. L-dopa was intensively studied using electrochemical sensors with applications in the biomedical field, pharmaceutical field and food industry. The determination of L-dopa is of great importance, due to the fact that it can cross the blood brain barrier (which dopamine can’t) and then can be converted to dopamine. Thus, it can be used in treating some disease, such as Parkinson’s. Because fast detective methods for L-dopa determination are required, this paper focused on four types of electrochemical sensors, such as modified carbon paste electrodes, modified glassy carbon electrodes, modified screen-printed electrodes and modified indium tin oxide electrodes. Each has its advantages and disadvantages and the appropriate sensor should be used depending on the type of application. [ABSTRACT FROM AUTHOR]

Herein, we report the environmental impact quantification of a newly developed fully printed electrochemical device to assist a colorimetric detection of phosphate in saliva. The evaluation of the analytical procedure was performed according to the principles of Green Analytical Chemistry and White Analytical Chemistry. The standard method for phosphate detection relies on a reaction between phosphate and molybdate in presence of antimony potassium tartrate and ascorbic acid, using strong acid conditions and high volumes of reagents (100–500 mL). To deliver an eco-friendly method, we have combined a screen-printed electrode with a liquid electrolyte battery and inkjet-printed conductive paths to develop a fully printed device on a flexible polymer substrate avoiding the use of ascorbic acid and using a small amount of reagents. The printed sensor was first developed and optimized for phosphate detection in saliva, allowing for a detection limit equal to 26 µM and satisfactory repeatability (relative standard deviation value of 7.5%). Finally, the AGREE and the RGB assessment tools were applied for a quantitative evaluation of the proposed sensor and reference method, in agreement with the Green Analytical and White Analytical principles. The results demonstrated the lower environmental impact of the proposed sensor, as well as the suitability of this novel approach for phosphate detection in saliva.

A novel simple, environmentally friendly and portable method to determine vitamin E in edible oils based on reversed-phase dispersive liquid-liquid microextraction combined with electrochemical detection using screen-printed carbon electrodes (SPCEs) has been developed. Vitamin E was extracted from oil samples into a 4 M HCl aqueous solution and determined by differential pulse voltammetry using SPCEs. The extraction conditions optimized by experimental design (i.e., Plackett–Burman and central composite designs) were: aqueous 4 M HCl extractant volume, 43 µL; extraction time, 2 min; centrifugation time, 10 min; and centrifugation speed, 3000 rpm. The proposed method requires a standard addition calibration approach, and the working range showed good linearity from 0 to 20 mg L−1, with a correlation coefficient ranging from 0.990 to 0.995 (N=5). The methodological limit of detection was between 1 and 3 mg L−1. The repeatability of the proposed method was evaluated at 15 mg L−1, and the relative standard deviation ranged between 10 and 15% (n=5). For the quantification of vitamin E in ten commercial samples of olive, sesame, soybean, sunflower and a mixture of sunflower and corn oils, the volume of the extractant phase (i.e., 4 M HCl aqueous solution) was increased up to 100 µL and satisfactory recoveries were obtained in the range of 85–115%, confirming the applicability of the method.

A two-dimensional (2D) Sb-modified screen-printed carbon nanofibers electrode (2D Sbexf-SPCNFE) was developed to improve the stripping voltammetric determination of Cd(II) and Pb(II), taking advantage of the synergistic effect between the two nanomaterials. The surface morphology of the 2D Sbexf-SPCNFE was investigated by scanning electron microscopy, energy-dispersive X-ray spectroscopy, and Raman spectroscopy. The analytical performance of 2D Sbexf-SPCNFE was compared to those presented by screen-printed carbon electrodes modified with 2D Sbexf (2D Sbexf-SPCE) and the corresponding bare electrodes: screen-printed carbon nanofibers electrode (SPCNFEbare) and screen-printed carbon electrode (SPCEbare). After optimizing the experimental conditions, the 2D Sbexf-SPCNFE exhibited much better analytical parameters compared to the other assessed sensors. Analysis in 0.01 mol L−1 HCl (pH = 2) using 2D Sbexf-SPCNFE showed excellent linear behavior in the concentration range of 2.9 to 85.0 µg L−1 and 0.3 to 82.0 µg L−1 for Cd(II) and Pb(II), respectively. The limits of detection after 240 s deposition time for Cd(II) and Pb(II) were 0.9 and 0.1 µg L−1, and sensitivities between 1.5 and 3 times higher than those displayed by SPCEbare, SPCNFEbare, and 2D Sbexf-SPCE were obtained. Finally, the 2D Sbexf-SPCNFE was successfully applied to the determination of Cd(II) and Pb(II) traces in a certified estuarine water sample.

Naphthol is a widely used chemical and medical detection biomarker, but it is harmful to human health and the environment. Therefore, a highly sensitive detection method for naphthol is urgently required. Herein, an electrochemical microsensor for the simultaneous detection of naphthol isomers was fabricated by the in situ growth of a three-dimensional graphene network (3DGN) on screen-printed electrodes. The microsensor exhibited good electrochemical sensing responses to typical isomers of naphthol (1-NAP and 2-NAP). Using the differential pulse voltammetry (DPV) method, the microsensor successfully realized the electrochemical detection of 1-NAP, 2-NAP, and naphthol isomer mixtures. Whether detecting naphthol isomers individually or simultaneously, the microsensor exhibited a good linear relationship for 1-NAP and 2-NAP in a wide range of concentrations. For the simultaneous detection of naphthol isomers, the limit of detection (LOD) of the microsensor to 1-NAP reached 10 nM, and the LOD for 2-NAP was about 20 nM. The microsensor also showed good selectivity, reproducibility, and stability. The simultaneous quantitative detection of 1-NAP and 2-NAP was also successfully achieved in synthetic urine samples.

We report on hydrogen peroxide sensors made through a single printing step with carbon ink containing catalytically synthesized Prussian blue nanoparticles. Despite their reduced sensitivity, the resulting bulk-modified sensors displayed both a wider linear calibration range (5 × 10−7–1 × 10−3 M) and an approximately four times lower detection limit versus the surface-modified sensors due to the dramatically decreased noise resulting in, on average, a six times higher signal-to-noise ratio. The corresponding glucose and lactate biosensors demonstrated similar and even higher sensitivities compared to those of biosensors based on surface-modified transducers. The biosensors have been validated through analysis of human serum. The decreased time and cost for production of single printing step bulk-modified transducers, as well as their analytical performance characteristics, which are advantageous over conventional surface-modified ones, would be expected to enable their wide use in (bio)sensorics.

Peroxynitrite anion (ONOO−) is an important in vivo oxidative stress biomarker whose aberrant levels have pathophysiological implications. In this study, an electrochemical sensor for ONOO− detection was developed based on graphene nanoplatelets-cerium oxide nanocomposite (GNP-CeO2) incorporated polyaniline (PANI) conducting hydrogels. The nanocomposite-hydrogel platform exhibited distinct synergistic advantages in terms of large electroactive surface coverage and providing a conductive pathway for electron transfer. Besides, the 3D porous structure of hydrogel integrated the GNP-CeO2 nanocomposite to provide hybrid materials for the evolution of catalytic activity towards electrochemical oxidation of ONOO−. Various microscopic and spectroscopic characterization techniques endorsed the successful formation of GNP-CeO2-PANI hydrogel. Cyclic voltammetry (CV) measurements of GNP-CeO2-PANI hydrogel modified screen-printed electrodes (SPE) were carried out to record the current changes influenced by ONOO−. The prepared sensor demonstrated a significant dose-dependent increase in CV peak current within a linear range of 5–100 µM (at a potential of 1.12 V), and a detection limit of 0.14 with a sensitivity of 29.35 ± 1.4 μA μM−1. Further, a customized microfluidic flow system was integrated with the GNP-CeO2-PANI hydrogel modified SPE to enable continuous electrochemical detection of ONOO− at low sample volumes. The developed microfluidic electrochemical device demonstrated an excellent sensitivity towards ONOO− under optimal experimental conditions. Overall, the fabricated microfluidic device with hybrid hydrogels as electrochemical interfaces provides a reliable assessment of ONOO− levels. This work offers considerable potential for understanding the oxidative stress–related disease mechanisms through determination of ONOO− in biological samples. [ABSTRACT FROM AUTHOR]

Screen-printed electrodes (SPEs) were produced using conductive inks based on hybrids of polyaniline (PAni) and reduced graphene oxide (rGO). Cyclic voltammetry (CV) showed peaks characteristic of the PAni redox behavior in acidic media for all the modified SPEs. Electrochemical impedance spectroscopy (EIS) showed a significant decrease in the charge-transfer resistances, from 930 Ω for SPE/G:PAni to 544 Ω for SPE/G:PAni-rGO1 and to 303 Ω for SPE/G:PAni-rGO2 with just 0.06% and 0.12% in mass of rGO, respectively, in the final mass composition of the conductive inks. The SPEs were evaluated in the determination of progesterone (P4) hormone in neutral medium (phosphate buffer solution, pH 7.0). The CV results showed higher current signals at SPE/G:PAni-rGO1 compared with SPE/G and SPE/G:PAni, indicating a synergistic effect of PAni-rGO1 in the determination of P4. EIS also showed significant changes in the electrochemical double-layer capacitances in the presence of P4. The limits of detection (LOD) and quantification (LOQ) were, respectively, 211 nmol l ^−1 and 703 nmol l ^−1 . This method is a simple, scalable and low-cost alternative for the fabrication of electrodes based on PAni-rGO hybrids, with synergic properties, aiming for future applications in sensors.

In this work, we propose a potentiometric smart sensor for lithium detection in environmental samples based on a screen-printed cell. The graphite screen-printed electrode (GSPE) was first modified by gold and silver nanoparticles to increase the conductivity, and then by an ion-selective membrane, which was directly deposited onto the nanostructured electrode surface. The potentiometric cell, thanks to its small size, was integrated with a portable instrument connected to a smartphone for decentralized analysis. The developed sensor was used in drop- and microflow-configurations and showed a high sensitivity for lithium with a low detection limit (1.6 µM). It was also applied in the analysis of real samples from the industrial recycling of automotive batteries and complex matrices, such as contaminated soils.

Irbesartan is a drug used to treat hypertension and high blood pressure. Recent studies associated sartans with several forms of cancer, making removing this class of substances from the environment a high priority. The EU has categorized drugs as emerging pollutants, and they can be more potent than other substances because they were designed to operate at low concentrations. Thus, effective and sensitive methods of determining Irbesartan selectively and accurately in environmental samples are necessary. MIPs have already been used to remove pollutants from complex matrixes, so they were also chosen for this work. In particular, a polyacrylate-based MIP was used to functionalize the graphite working electrode of screen-printed cells (SPCs), aiming to develop a voltammetric method for Irbesartan sensing. The MIP composition and the experimental conditions for the electrochemical determination were optimized through a Design of Experiments (DoE) approach. The whole analysis was replicated with different SPCs obtaining similar results, which highlight the good reproducibility potential. MIP-based electrodes were also applied to determine Irbesartan in fortified tap water samples, obtaining high recovery percentages. Given the good results, the electrochemical method based on MIP-modified screen-printed electrodes is promising for quantifying Irbesartan at a trace level.

2,4-Dichlorophenoxyacetic acid (2,4-D) is a widely used herbicide worldwide. However, its residues in agricultural products are extremely harmful to human health and to the environment in soil and water. Previous methods for determining 2,4-D in water and soil samples are expensive, cumbersome, and not highly selective. In this study, we developed a novel disposal sensor based on screen-printed electrodes (SPEs) for detecting 2,4-D in wastewater and soil samples. The SPEs were modified with conductive polyaniline (PANI) layer and polyvinyl chloride (PVC) membrane loaded with molecularly printed polymer (MIP). The MIP particles were prepared using 2,4-D as template, methacrylic acid (MAA) as monomer, ethylene glycol dimethacrylate (EGDMA) as cross-linker, and benzoyl peroxide as initiator. The best sensor shows a dynamic concentration range of 10−2 to 10−7 M 2,4-D, a detection limit (LOD) of 3.6 × 10−7 M, Nernst slope (response) of 29.9 mV/decade, and high selectivity over other interfering species previously reported in the literature. The sensors also achieved a short response time of 25 s, high reversibility, and a lifetime of over 2 weeks. The developed sensors were successfully used for determining 2,4-D in real wastewater and soil samples with high accuracy and precision.

Monitoring the concentration of antibiotics in body fluids is essential to optimizing the therapy and minimizing the risk of bacteria resistance, which can be made with electrochemical sensors tailored with appropriate materials. In this paper, we report on sensors made with screen-printed electrodes (SPE) coated with fullerene (C60), reduced graphene oxide (rGO) and Nafion (NF) (C60-rGO-NF/SPE) to determine the antibiotic metronidazole (MTZ). Under optimized conditions, the C60-rGO-NF/SPE sensor exhibited a linear response in square wave voltammetry for MTZ concentrations from 2.5 × 10−7 to 34 × 10−6 mol/L, with a detection limit of 2.1 × 10−7 mol/L. This sensor was also capable of detecting MTZ in serum and urine, with recovery between 94% and 100%, which are similar to those of the standard chromatographic method (HPLC-UV). Because the C60-rGO-NF/SPE sensor is amenable to mass production and allows for MTZ determination with simple principles of detection, it fulfills the requirements of therapeutic drug monitoring programs. [Display omitted] • Determination of metronidazole (MTZ) in urine and synthetic serum sample. • The MTZ is a synthetic antibiotic widely used for surgical prophylaxis, in patients with burn wounds and other pathologies. • The detection of MTZ is relevant to minimize its side effects and avoid acquired resistance. • We employed fullerene C60-rGO and nafion in low-cost screen-printed electrode (SPE). • Electrochemical sensor is amenable to mass production. [ABSTRACT FROM AUTHOR]

A methodology is presented to develop tungsten-oxide based inks for screen-printing. Different amounts of tungsten oxide have been grown by co-precipitation on the surface of conducting microparticles. These modified particles have been formulated into inks, and electrodes have been screen-printed. The work describes the characterization of the materials using a range of techniques including XRD, SEM, as well as electrochemical and spectroscopic techniques. Thermal treatment of the co-precipited oxides changes their crystalline structure, increasing bandgap (from 2.48 eV to 2.87 eV) and worsening their electrochromic performance. Structures printed with untreated WO 3 -based materials display contrast ratios as high as 90 % in reflectance, and colour efficiencies between 30 and 40 cm2 C–1. Another important aspect is the pH stability of the oxide up to pH = 6. [ABSTRACT FROM AUTHOR]

Triple-negative breast cancer (TNBC) is one of the most aggressive and lethal types of BC, affecting mostly young women and its diagnosis is difficult and requires invasive methods, such as tissue biopsy which is painful and expensive. However, nowadays liquid biopsy is emerging as a great tool for determining blood-circulating species associated to cancer and to its early diagnosis and prognosis. Among the species, the relevance of microRNAs (miRNAs) has been highlighted as promising biomarker, and miRNA-652 has been associated with TNBC as it promotes the growth and migration of cancer cells. In this work we designed and characterized a paper-based electrochemical device capable of recognizing and quantifying miRNA-652, as future tool for liquid biopsy in TNBC. The device consists of an AuNP-modified office paper-based screen-printed electrode customized with an anti-miRNA probe for the selective recognition of miRNA-652. All the experimental parameters have been carefully evaluated, and the platform allowed to detect miRNA-652 in standard solution and human serum down to 0.4 nM, with a satisfactory repeatability of about 6 and 3 % respectively. The selectivity presence of other miRNA sequences was satisfactory demonstrated. In addition, we demonstrated the effectiveness of pre-concentration of miRNA by coupling the office paper-based electrode with an external disk made by chromatographic paper: the detection limit has been improved of 10-fold without the use of complex/expensive procedures. The presented manuscript represents an important step towards the development of a non-invasive, sensitive and TNBC-specific diagnostic platform that could improve patients' prognosis and quality of life, ulteriorly improved with pre-concentering properties of frugal supports as the external chromatographic paper-based ones. [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] • Carbon nanofibers efficiently functionalized via easy and rapid microwave approach. • f-CNF MW perform electrochemically better than conventional f-CNF Refluxed. • f-CNF MW sensing materials show excellent electrocatalytic activity for redox analytes. • f-CNF MW show strong quality features: selectivity, sensitivity, and fouling resistance. This research introduces a novel approach for swiftly enhancing the electrochemical sensing capabilities of commercial screen-printed carbon electrodes through a rapid acid microwave-assisted functionalization of carbon nanofibers (f-CNF MW). A comparative analysis with the conventional refluxed system functionalization method (f-CNF Refluxed) was conducted to assess the electrochemical performance of the newly developed f-CNF MW. The voltametric study showed that f-CNF- MW significantly enhanced the electron transfer rate when testing common phenolic compounds such as hydroquinone, paracetamol, and caffeic acid. Moreover, the anodic oxidation potential for the majority of irreversible analytes was negatively shifted, indicating the high electro-catalytic activity of f-CNF- MW gained after this treatment, making it analytically useful for the electro-oxidation of some molecules that require high overpotential, mainly for purine bases and nitrite. Additionally, the developed f-CNF- MW exhibited remarkable resistance to fouling phenomena when exposed to bisphenol A and tryptophan, underscoring its potential for real-world applications. To sum up, this study highlights the potential of rapid microwave treatment in producing f-CNF- MW as a promising electrochemical nanomaterial, resulting in substantial improvements in electro-analytical capabilities compared to conventional methodologies. [ABSTRACT FROM AUTHOR]