This study explores the development of a non-enzymatic electrochemical glucose sensor based on poly(3-aminobenzoic acid) (P3ABA) combined with silver nanoparticles (AgNPs). Incorporating AgNPs into the P3ABA matrix enhances the sensor’s electrocatalytic properties, leading to a system with greater stability. Cyclic voltammetry and chronoamperometry were employed to evaluate the sensor’s performance, demonstrating a sensitivity of 50.71 µA mM⁻¹ cm⁻² and a limit of detection (LOD) of 0.2 µM. The sensor exhibited a linear response over a broad concentration range (1 to 16 mM), with a coefficient of determination (R²) of 0.998, indicating good reproducibility and precision. These results highlight the potential of the P3ABA/AgNP composite for glucose sensing applications, offering an extended linear range, allowing for the quantification of glucose concentrations from very low to significantly high levels, covering both physiological and pathological conditions.

The present work describes the synthesis of an electroactive nanocomposite consisting of carbon black (CB) and polyaniline (PANI) obtained by in situ oxidative polymerization. Monomer P1 was used as a polyaniline precursor. P1 has surfactant properties that allow obtaining core–shell structures dispersed in an aqueous medium. The nanocomposite, together with silver nanoparticles (AgNPs) as an electrocatalytic element, was used to modify the surface of a glassy carbon electrode (GCE) for glucose detection. Electroactive areas were calculated using the Randles–Sevick equation. The results showed that the CB-PANI.1-1/AgNP nanocomposite exhibited a larger electroactive surface area (0.3451 cm²) compared to AgNP alone (0.0973 cm²) or the CB-PANI.1-1 composite (0.2989 cm²). Characterization of CB-PANI.1-1/AgNP, by cyclic voltammetry in the presence of glucose, showed a new oxidation peak with a maximum current close to 0.7 V due to the oxidation of glucose to gluconolactone. The amperometry test at 0.7 V showed a linear response with R² of 0.999 as a function of the analyte concentration. The glucose sensor presented a linear detection range of 1 to 10 mM, a sensitivity of 41 µA mM⁻¹ cm⁻², and a limit of detection (LOD) of 520 µM.

Agro-industrial wastes such as wheat husk (WH) are renewable sources of organic and inorganic substances, including cellulose, lignin, and aluminosilicates, which can be transformed into advanced materials with high added value. The use of geopolymers is a strategy to take advantage of the inorganic substances by obtaining inorganic polymers, which have been used as additives, e.g., for cement and refractory brick products or ceramic precursors. In this research, the WH native to northern Mexico was used as a source to produce wheat husk ash (WHA) following its calcination at 1050 °C. In addition, geopolymers were synthesized from the WHA by varying the concentrations of the alkaline activator (NaOH) from 16 M to 30 M, namely Geo 16M, Geo 20M, Geo 25M, and Geo 30M. At the same time, a commercial microwave radiation process was employed as the curing source. Furthermore, the geopolymers synthesized with 16 M and 30 M of NaOH were studied for their thermal conductivity as a function of temperature, in particular at 25, 35, 60, and 90 °C. The chemical composition of the WHA, determined by ICP, revealed a SiO₂ content close to 81%, which is similar to rice husk. The geopolymers were characterized using various techniques to determine their structure, mechanical properties, and thermal conductivity. The findings showed that the synthesized geopolymers with 16M and 30M of NaOH had significant mechanical properties and thermal conductivity, respectively, compared to the other synthesized materials. Finally, the thermal conductivity regarding the temperature revealed that Geo 30M presented significant performance, especially at 60 °C.

Lithium niobate perovskite and silver nanoparticle-based nanocomposites (LNB:AgNPs) were explored for developing an electrochemical glucose sensor. The perovskite to silver nanoparticle ratios investigated were 4:1, 1:1, 1:2, 2:1, and 1:4. Among these, the 4:1 ratio, with the lowest silver content, demonstrated the most stable performance during glucose quantification via amperometry. The sensor’s response was evaluated measuring the current at a fixed potential of 0.7 V following the injection of 1 mM glucose with each addition. The calibration curve obtained from the recorded data exhibited a linear response within the 1 to 15 mM glucose concentration range, achieving a sensitivity of 2 μA/mM, a high correlation coefficient (R² = 0.997), and a limit of detection (LOD) of 0.5 µM. The LNB4:1AgNP composite allowed taking advantage of the unique properties of both components in a balanced manner, maximizing the sensor performance in practical applications.

The Volume 1, Issue 1 published for IJTAN Journal.

The structural modification of biopolymers is a current strategy to develop materials with biomedical applications. Silk fibroin is a natural fiber derived from a protein produced by the silkworm (Bombyx mori) with biocompatible characteristics and excellent mechanical properties. This research reports the structural modification of silk fibroin by incorporating polyaniline chain grafts through a one-pot process (esterification reaction/oxidative polymerization). The structural characterization was achieved by ¹H-NMR and FT-IR. The morphology was studied by scanning electron microscopy and complemented with thermogravimetric analysis to understand the effect of the thermal stability at each step of the modification. Different fibroin silk (Fib): polyaniline (PAni) mass ratios were evaluated. From this evaluation, it was found that a Fib to PAni ratio of at least 1 to 0.5 is required to produce electroactive polyaniline, as observed by UV-vis and CV. Notably, all the fibroin-g-PAni systems present low cytotoxicity, making them promising systems for developing biocompatible electrochemical sensors.