Despite the fact that a considerable amount of effort has been invested in the development of biosensors for the detection of pesticides, there is still a lack of a simple and low-cost platform that can reliably and sensitively detect their presence in real samples. Herein, an enzyme-based biosensor for the determination of both carbamate and organophosphorus pesticides is presented that is based on acetylcholinesterase (AChE) immobilized on commercially available screen-printed carbon electrodes (SPEs) modified with carbon black (CB), as a means to enhance their conductivity. Most interestingly, two different methodologies to deposit the enzyme onto the sensor surfaces were followed; strikingly different results were obtained depending on the family of pesticides under investigation. Furthermore, and towards the uniform application of the functionalization layer onto the SPEs’ surfaces, the laser induced forward transfer (LIFT) technique was employed in conjunction with CB functionalization, which allowed a considerable improvement of the sensor’s performance. Under the optimized conditions, the fabricated sensors can effectively detect carbofuran in a linear range from 1.1 × 10⁻⁹ to 2.3 × 10⁻⁸ mol/L, with a limit of detection equal to 0.6 × 10⁻⁹ mol/L and chlorpyrifos in a linear range from 0.7 × 10⁻⁹ up to 1.4 × 10⁻⁸ mol/L and a limit of detection 0.4 × 10⁻⁹ mol/L in buffer. The developed biosensor was also interrogated with olive oil samples, and was able to detect both pesticides at concentrations below 10 ppb, which is the maximum residue limit permitted by the European Food Safety Authority.

This work reports the fabrication of integrated electrochemical fluidic paper-based analytical devices (ePADs) using a marker pen drawing and screen-printing. Electrodes were deposited on paper using screen-printing with conductive carbon ink. Then, the desired fluidic patterns were formed on the paper substrate by drawing with a commercial hydrophobic marker pen using an inexpensive computer-controlled x-y plotter. The working electrode was characterized by cyclic voltammetry and scanning electron microscopy. The analytical utility of the electrochemical PADs is demonstrated through electrochemical determination of Pb(II) and Cd(II) by anodic stripping voltammetry. For this purpose, the sample was mixed with a buffer solution and a Bi(III) solution, applied to the test zone of the PAD, the metals were preconcentrated as a bismuth alloy on the electrode surface and oxidized by applying an anodic potential scan. The proposed manufacturing approach enables the large-scale fabrication of fit-for-purpose disposable PADs at low cost which can be used for rapid on-site environmental monitoring.

This work reports the development and optimization of a rapid and low-cost pen-on-paper plotting approach for the fabrication of paper-based analytical devices (PADs) using commercial writing stationery. The desired fluidic patterns were drawn on the paper substrate with commercial marker pens using an inexpensive computer-controlled x–y plotter. For the fabrication of electrochemical PADs, electrodes were further deposited on the devices using a second x–y plotting step with commercial writing pencils. The effect of the fabrication parameters (type of paper, type of marker pen, type of pencil, plotting speed, number of passes, single- vs. double-sided plotting), the chemical resistance of the plotted devices to different solvents and the structural rigidity to multiple loading cycles were assessed. The analytical utility of these devices is demonstrated through application in optical sensing of total phenols using reflectance calorimetry and in electrochemical sensing of paracetamol and ascorbic acid. The proposed manufacturing approach is simple, low cost, flexible, rapid and fit-for-purpose and enables the fabrication of sub-“one-dollar” PADs with satisfactory mechanical and chemical resistance and good analytical performance.

In this work, we describe a new type of electrochemical aptasensor for the label-free detection of oxytetracycline (OTC). Thin-film gold electrodes were fabricated through sputtering gold on a Kapton film, followed by the immobilization of a thiol-modified aptamer on the electrode surface. The selective capture of OTC at the aptamer-functionalized electrodes was monitored electrochemically with the use of the [Fe(CN)₆]⁴⁻/[Fe(CN)₆]³⁻ redox probe. Different experimental variables were studied, through which the metrological features for OTC determination were derived. Finally, the developed sensor was implemented to achieve the detection of OTC in a spiked milk sample.

In this work, we describe the fabrication of paper-based aptasensing devices for ampicillin determination that rely on the salt-induced aggregation of gold nanoparticles (AuNPs) in the presence of the target. Circular paper-based devices were created on paper via pen-plotting (using water-repellent ink to create hydrophobic barriers) and modified with NaCl. The sample was incubated with an ampicillin aptamer and AuNPs and was added to the assay zones of the paper-based devices. In the absence of ampicillin, the aptamer prevented the aggregation of the AuNPs, and the assay zones remained red. When ampicillin was present, it selectively bound with the aptamer and the AuNP aggregate, producing a purple color. The color of the assay zones was monitored via a smartphone, and the color graduation was related to the ampicillin concentration in the sample. Different experimental parameters (type of paper, concentration of reagents) were investigated, and the analytical features of the method for the determination of ampicillin were established.

In this work, a “green” electrochemical paper-based device (ePAD) for the voltammetric determination of Tl(I) is described. A mini voltammetric cell was patterned on chromatographic paper by using screen printing to deposit three carbon electrodes and plotting with hydrophobic ink to form a circular assay zone. The sample was added to the assay zone (which was pre-loaded with Bi(III)) and Tl(I) was quantified using anodic stripping voltammetry (ASV). The experimental conditions and potential interferences were studied. The limit of detection was at the low μg L⁻¹ level, indicating that these devices can serve successfully as fit-for-purpose disposable voltammetric sensors for Tl(I).