A graphene and poly (3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) modified conductive paper-based electrochemical impedance spectroscopy (EIS) aptasensor has been successfully fabricated by a simple and continuous coating process. A graphene/PEDOT:PSS modified paper electrode forms the nanocomposite providing a conductive and sensitive substrate for further aptamer functionalization of the biosensor. This low-cost paper-based aptasensor exhibits its sensitivity to carcinoembryonic antigens (CEA) in standard buffer solutions and human serum samples in a linear range of 0.77–14 ng·mL⁻¹. The limit of detection (LOD) is found to be 0.45 ng·mL⁻¹ and 1.06 ng·mL⁻¹ for CEA in both samples, separately. This aptamer-based sensing device was also evaluated and received a good correlation with the immunoassay detection method. The proposed paper-based aptasensor has demonstrated its potential as a rapid simple point-of-care analytical platform for early cancer diagnosis in less developed areas where manufacturing facilities, analytical instruments, and trained specialists are limited.

Heavy metal ion pollution has had a serious influence on human health and the environment. Therefore, the monitoring of heavy metal ions is of great practical significance. In this work, we describe the development of an electrochemical sensor to detect cadmium (Cd²⁺) using a Prussian blue (PB), poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT)-loaded laser-scribed graphene (LSG) nanocomposite-modified glassy carbon electrode (GCE). In this nanocomposite material, we successfully brought together the advantages of an extraordinarily large surface area. The accumulation of PB nanoparticles results in an efficient electrochemical sensor with high sensitivity and selectivity and fast detection ability, developed for the trace-level detection of Cd²⁺. Electrochemical features were explored via cyclic voltammetry (CV), whereas the stripping voltammetry behavior of modified electrodes was analyzed by utilizing differential pulse voltammetry. Compared with bare GCE, the LSG/PB-PEDOT/GCE modified electrode greatly increased the anodic stripping peak currents of Cd²⁺. Under the optimized conditions, the direct and facile detection of Cd²⁺ was achieved with a wide linear range (1 nM–10 µM) and a low LOD (0.85 nM).

The analysis of pharmaceutical active ingredients plays an important role in quality control and clinical trials because they have a significant physiological effect on the human body even at low concentrations. Herein, a flexible three-electrode system using laser-scribed graphene (LSG) technology, which consists of Nafion/Fe₃O₄ nanohybrids immobilized on LSG as the working electrode and LSG counter and reference electrodes on a single polyimide film, is presented. A Nafion/Fe₃O₄/LSG electrode is constructed by drop coating a solution of Nafion/Fe₃O₄, which is electrostatically self-assembled between positively charged Fe₃O₄ and negatively charged Nafion on the LSG electrode and is used for the first time to determine a neurotoxicity drug (clioquinol; CQL) in biological samples. Owing to their porous 3D structure, an enriched surface area at the active edges and polar groups (OH, COOH, and -SO₃H) in Nafion/Fe₃O₄/LSG electrodes resulted in excellent wettability to facilitate electrolyte diffusion, which gave ∼twofold enhancement in electrocatalytic activity over LSG electrodes. The experimental parameters affecting the analytical performance were investigated. The quantification of clioquinol on the Nafion/Fe₃O₄/LSG electrode surface was examined using differential pulse voltammetry and chronoamperometry techniques. The fabricated sensor displays preferable sensitivity (17.4 μA μM^-1 cm^-2), a wide linear range (1 nM to 100 μM), a very low detection limit (0.73 nM), and acceptable selectivity toward quantitative analysis of CQL. Furthermore, the reliability of the sensor was checked by CQL detection in spiked human blood serum and urine samples, and satisfactory recoveries were obtained.

This study demonstrates a novel method for electrical detection of C-reactive protein (CRP) as a means of identifying an infection in the body, or as a cardiovascular disease risk assay. The method uses a single free-standing, thermally controlled piezoresistive microcantilever biosensor. In a commonly used sensing arrangement of conventional dual cantilevers in the Wheatstone bridge circuit, reference and gold-coated sensing cantilevers that inherently have heterogeneous surface materials and different multilayer structures may yield independent responses to the liquid environmental changes of chemical substances, flow field and temperature, leading to unwanted signal disturbance for biosensing targets. In this study, the single free-standing microcantilever for biosensing applications is employed to resolve the dual-beam problem of individual responses in chemical solutions and, in a thermally controlled system, to maintain its sensor performance due to the sensitive temperature effect. With this type of single temperature-controlled microcantilever sensor, the electrical detection of various CRP concentrations from 1 µg/mL to 200 µg/mL was performed, which covers the clinically relevant range. Induced surface stresses were measured at between 0.25 N/m and 3.4 N/m with high reproducibility. Moreover, the binding affinity (K_D) of CRP and anti-CRP interaction was found to be 18.83 ± 2.99 µg/mL, which agreed with results in previous reported studies. This biosensing technique thus proves valuable in detecting inflammation, and in cardiovascular disease risk assays.