Gabriela V. Martins

Nature offers a robust conceptual framework for designing next-generation adaptive, multifunctional sensing systems. Also, in sensing systems, Trojan materials add a functional dimension to the microstructure, enabling the development of high-performance humidity sensors without interfering with their macrostructure. Thus, based on a brief overview of how inspiration from plants, animals, and membranes can be used to engineer high-performance platforms for environmental humidity monitoring, combined with the functional dimension of Trojan materials, this review presents a critical framework detailing the key developments in the main categories of self-sensing materials within the scope of humidity sensors. The review addresses electronically and ionically conductive polymers, polymer composites with dispersed active fillers, and hydrogel-based or other water-compatible systems. Additionally, commercially available sensors are described, and the main challenges and future directions are identified.

This research presents a novel, cost-effective, and scalable approach for the direct detection of myoglobin (Myo) in point-of-care (PoC) applications. In this strategy, redox-active Prussian Blue nanocubes (PBNCs) are applied to a disposable platinum screen-printed electrode (Pt-SPE). Subsequently, a biomimetic sensing layer is generated by electropolymerization of ortho-phenylenediamine (o-PD) in the presence of Myo, which forms molecularly imprinted polymer (MIP) sites by cyclic voltammetry (CV). The electropolymerization process takes place in a potential range of −0.2 V to +0.8 V, for five cycles at a scan rate of 50 mV/s, in a 10 mmol/L o-PD solution. After polymerization, the electrode is incubated in trypsin for 2 h to create Myo-specifically imprinted cavities. The structural and morphological properties of the biomimetic layer were analyzed by Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The direct detection of Myo was analyzed by differential pulse voltammetry (DPV). The results showed a linear response to Myo concentrations ranging from 1.0 ag/mL to 10 ng/mL, a limit of detection (LOD) of 0.76 ag/mL, and a R² value of 0.9775. The absence of an external liquid redox probe simplifies the sensor design, improves portability, and reduces the complexity of the assay, making it more suitable for PoC.

A cutting-edge biosensor has been developed to monitor blood glucose levels, which is particularly vital for people with diabetes. This advanced technology uses a miniaturized and membraneless enzymatic fuel cell (EFC) as a compact electrical reader for rapid on-site diabetes diagnosis. Using disposable screen-printed gold electrodes (Au-SPE) modified with the enzyme glucose oxidase (GOx), the biosensor enables the oxidation of glucose at both the anode (counter electrode) and cathode (working electrode) of the EFC. The cathode contains graphene oxide/Prussian blue nanocubes (GO/PBNCs), while the anode uses a biographene layer. Both electrodes were modified with GOx by electrostatic/hydrogen bonding the enzyme to the modified electrodes surface. Individual evaluations of each electrode system emphasized their effectiveness. The integration of both electrodes resulted in an EFC that can generate an output power of approximately 1.8 μW/cm² at a glucose concentration of 5 mmol/L, which is very close to physiological conditions (3.8 to 6.9 mmol/L). This technology represents a significant advance and promises fully autonomous diagnostic devices suitable for a wide range of analytes. It paves the way for diagnostics everywhere and marks a fundamental shift in point-of-care (PoC) diagnostics.

Addressing global challenges in wound management has greatly encouraged the emergence of home diagnosis and monitoring devices. This technological shift has accelerated the development of new skin patch sensors for continuous health monitoring. A key requirement is the creation of flexible platforms capable of mimicking human skin features. Here, for the first time, an innovative, highly adaptable electrochemical biosensor with molecularly imprinted polymers (MIPs) is customized for the detection of the inflammatory biomarker interleukin‐6 (IL‐6). The 3‐electrode gold pattern is geometrically standardized onto a 6 µm thick polyimide flexible membrane, an optically transparent, and biocompatible polymeric substrate. Subsequently, a biomimetic sensing layer specifically designed for the detection of IL‐6 target is produced on these transducers. The obtained MIP biosensor shows a good linear response within the concentration range 50 pg mL⁻¹‐50 ng mL⁻¹, with a low limit of detection (8 pg mL⁻¹). X‐ray photoelectron spectroscopy, scanning electron microscopy, and Fourier transform infrared spectroscopy characterizations confirm the modifications of the flexible gold transducer. After optimization, the biosensing device shows remarkable potential in terms of sensitivity, selectivity, and reproducibility. Overall, the integration of a low‐cost electrochemical sensor on biocompatible flexible polymers opens the way for a new generation of monitoring tools with higher accuracy, less invasiveness, and greater patient comfort.

In recent years, flexible electronics have experienced a massive growth as a response to the high demand for new skin-patch sensor devices targeted at personal health-monitoring. In this context, the incorporation of biopolymers into the backbone of these soft systems brings new opportunities in terms of biocompatibility and sustainability performance. However, the suitable integration of a conductive patterned material is still a challenge, in order to achieve good adhesion and high transparency. Thus, silver nanowires (AgNWs) constitute promising candidates for the fabrication of flexible transparent conductive films. Herein, a chitosan membrane doped with a plasticizer element was made conductive, through a one-step process, by using an optimized ratio of chitosan–lactic acid–AgNWs (Chi-LaA-AgNWs) dispersion. This formulation was applied using screen-printing, and the influence of the polymer ratio, cure temperature, and number of layers applied with the AgNW-based ink was investigated. Compared with conventional water-based AgNW dispersions, the here-proposed chitosan-doped ink enabled the fabrication of transparent electrode platforms holding good stability, homogeneity, and electrical features.