Chemosensors

In this work, a potentiometric sensor for the detection of biogenic amines (BAs) in food samples was developed and characterised. The sensor employs a home-fabricated electrode incorporating a cucurbit[6]uril-modified polyvinyl chloride membrane as the sensing element. The working principle, system behaviour, and optimal operational conditions for BA monitoring were systematically investigated. The developed sensor demonstrated excellent analytical performance, showing a linear response in the concentration range of 3.0 × 10⁻⁵ to 1.0 × 10⁻² mol L⁻¹, with a low limit of detection of 2.4 × 10⁻⁵ mol L⁻¹. Among the tested analytes, the sensor exhibited the highest sensitivity toward tyramine. These results highlight the potential of the proposed cucurbit[6]uril-based potentiometric sensor as an effective and reliable tool for monitoring BAs in complex food matrices, contributing to improved food safety, quality control, and spoilage prevention in the food industry, while also demonstrating its new application as a low-cost, easily constructed platform for rapid tyramine screening in food products.

Creatinine (Crn) is a clinically relevant biomarker commonly used for the diagnosis and monitoring of kidney disease. In this work, we report the fabrication of reduced-graphene-oxide-based field-effect transistors (rGO FETs) for Crn detection. These devices were functionalized using a layer-by-layer (LbL) assembly, in which polyethyleneimine (PEI) and creatinine deiminase (CD) were alternately deposited. This LbL strategy allows for the effective incorporation of CD without compromising its structural or functional integrity, while also taking advantage of the local pH changes caused by creatinine hydrolysis. It also benefits from the use of a polyelectrolyte that can amplify the enzymatic signal. Furthermore, it enables scalable and efficient fabrication. These transistors also address the challenges of point-of-care implementation in single-use cartridges. It is worth noting that the devices showed a linear relationship between the Dirac-point shift and the logarithm of the creatinine concentration in the 20–500 µM range in diluted simulated urine. The sensor response improved with increasing numbers of PEI/CD bilayers. Furthermore, the functionalized FETs demonstrated rapid detection dynamics and good long-term stability. Present results confirm the potential of these devices as practical biosensors for sample analysis under real-world conditions, making them ideal for implementation in practical settings.

This work presents the design of a novel electrochemical sensor for highly sensitive determination of LEV, utilizing a sensing platform based on a newly synthesized, high-purity manganese (III) porphyrin complex [5,10,15,20-tetrayltetrakis(2-methoxybenzene-4,1-diyl) tetraisonicotinateporphyrinato] manganese (III) porphyrin (MnTMIPP). The successful synthesis of the MnTMIPP complex was verified using ultraviolet–visible (UV–Vis) and infrared spectroscopy (IR). The sensing electrode was fabricated by depositing the synthesized material onto an indium tin oxide (ITO) electrode via a drop-coating method. Under optimized experimental conditions, the proposed sensor demonstrated a wide dynamic range, from 10⁻⁹ M to 10⁻³ M, with a low calculated detection limit of 4.82 × 10⁻¹⁰ M. Furthermore, the MnTMIPP/ITO electrode displayed interesting metrological performance: high selectivity, reproducibility, and stability. Successful application in spiked river water and saliva samples with satisfactory recovery rates confirms the sensor’s potential as a reliable and cost-effective platform for monitoring LEV in real-world environments.