Glucose measurement is a fundamental tool in the daily care of Diabetes Mellitus (DM) patients and healthcare professionals. While there is an established market for glucose sensors, the rising number of DM cases has promoted intensive research to provide accurate systems for glucose monitoring. Polyaniline (PAni) is a conductive polymer with a linear conjugated backbone with sequences of single C–C and double C=C bonds. This unique structure produces attractive features for the design of sensing systems such as conductivity, biocompatibility, environmental stability, tunable electrochemical properties, and antibacterial activity. PAni-based glucose sensors (PBGS) were actively developed in past years, using either enzymatic or non-enzymatic principles. In these devices, PAni played roles as a conductive material for electron transfer, biocompatible matrix for enzymatic immobilization, or sensitive layer for detection. In this review, we covered the development of PBGS from 2015 to the present, and it is not even exhaustive; it provides an overview of advances and achievements for enzymatic and non-enzymatic PBGB PBGS for self-monitoring and continuous blood glucose monitoring. Additionally, the limitations of PBGB PBGS to advance into robust and stable technology and the challenges associated with their implementation are presented and discussed.

The high incidence of Diabetes Mellitus in low-income regions has promoted the development of low-cost alternatives to replace blood-based procedures. In this work, we present a bienzymatic paper-based sensor suitable for the naked-eye detection of glucose in saliva samples. The sensor was obtained by a stamping procedure and modified with chitosan to improve the colorimetric readout. The bienzymatic reaction of GOx-HRP coupled with 2,4,6-tribromo-3-hydroxy benzoic acid was applied for the detection of glucose within a range from 0 to 180 mgdL⁻¹ in buffer and artificial saliva solutions. The visual readout was perceived by the naked eye and registered with an office scanner to evaluate the analytical performance. The results showed a limit of detection of 0.37 mgdL⁻¹ (S/N = 3) with an R.S.D. of 1.69% and a linear range from 1 to 22.5 mgdL⁻¹ with an R² of 0.99235. The analysis of human saliva samples was performed without pre-processing, achieving recoveries from 92 to 114%. The naked-eye detection was evaluated under two different light settings, showing average recoveries of 108.58 and 90.65% for standard and low illumination. The proposed device showed potential for easy-to-use, sensitive, low-cost, fast, and device-free detection of salivary glucose suitable for untrained personnel operation and limited facilities.

The tailoring of novel nanomaterials for sensitive glucose detection through a non-enzymatic mechanism is currently under intensive research. Here, we present a laser-induced graphene (LIG) electrode decorated with silver nanoparticles (AgNPs) as a catalytic element for the direct electrooxidation of glucose. The AgNPs were synthesized through cyclic voltammetry using LIG as a template, resulting in a porous tridimensional assembly with anchored nanostructures. The characterization corroborated the formation of LIG/AgNPs composite with distinctive peaks attributed to Ag₂O and AgO interaction with glucose. The proposed non-enzymatic sensors were successfully applied for non-enzymatic amperometric detection, exhibiting a linear range from 1 to 10 mM in the first peak (+0.7 V) and a narrow range from 1 to 2 mM with higher sensitivity of 52.2 mA/mM and improved LOD of 45 μM in the second peak (+0.55 V). The applicability of the LIG/AgNPs sensor was evaluated with spiked artificial saliva in a PoC format using a smartphone potentiostat, showing an average recovery rate of 91%. The analysis was performed in a portable, mobile, and low-cost fashion using a simulated non-invasive sample, with promising results in clinical ranges.

Although an enzymatic electrochemical biosensor is a major keystone in Diabetes Mellitus management, its replacement with a low-cost and stable non-enzymatic glucose sensor (NEGS) is of high interest to scientific and industrial fields. However, most NEGS for direct glucose electrooxidation (DGE) must be performed under extreme alkaline conditions, implying additional pretreatments before detection and a limited application for on-body, real-time monitoring. Thus, research on DGE in physiological conditions is fundamental to successfully translating the current NEGS into clinical applications. In physiological conditions, drawbacks such as low current, low selectivity, and poisoning appear due to the reduction of OH ions in neutral electrolytes and the presence of chloride ions in biofluids. Therefore, an increasing number of nanomaterials based on Pt, Au, and their nanocomposites have been proposed to improve the electrochemical performance. Additionally, transition metals such as Cu, Pd, Ni, or Co combined with high surface area supports have shown promising results in increasing catalytic sites for DGE. The molecular interaction of phenylboronic acid with glucose has also been demonstrated in neutral conditions. Overall, the present review summarizes the current strategies for DGE in physiological conditions and highlights the challenges still faced for further development of functional glucose NEGS.

Chemical sensing based on semiconducting metal oxides has been largely proposed for acetone sensing, although some major technical challenges such as high operating temperature still remain unsolved. This work presents the development of an electrochemical sensor based on nanostructured PANI/cellulose/WO₃composite for acetone detection at room temperature. The synthesized materials for sensor preparation were polyaniline (PANI) with a conductivity of 13.9 S/cm and tungsten trioxide (WO₃) in monoclinic phase doped with cellulose as carbon source. The synthesized materials were characterized by high resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), cyclic voltammetry (CV), and Raman spectroscopy. The composite was applied for acetone detection in the range of 0 to 100 ppmv at room temperature with electrochemical impedance spectroscopy (EIS) for monitoring resistance changes proportional to acetone concentration. The developed sensor achieved a calculated limit of detection of 10 ppm andR2of 0.99415 with a RSD of 5% (n=3) at room temperature. According to these results, the developed sensor is suitable for acetone sensing at room temperatures without the major shortcomings of larger systems required by high operating temperatures.