DNA Aptamer Integrated Hydrogel Nanocomposites on Screen Printed Gold Electrodes for Point-of-Care Detection of Testosterone in Human Serum.

This work describes the development and evaluation of a novel electrochemical aptasensor for testosterone detection. The sensor utilizes a specifically designed DNA immobilized on a screen-printed gold electrode (SPGE) modified with a conductive hydrogel and gold nanoparticles (HG/NP) composite. The aptasensor exhibited a dose-dependent response to testosterone (0.05 to 50 ng/mL) with a detection limit of 0.14 ng/mL and a good sensitivity of 0.23 µA ng-1 mL cm-2. The sensor displayed excellent selectivity towards testosterone compared to structurally similar steroid hormones. Importantly, the incorporation of HG/NP not only improved the sensor's conductivity but also acted as an antifouling layer, minimizing signal interference from non-specific biomolecule interactions in complex biological samples like human serum. The results obtained from the aptasensor showed good correlation with a standard ELISA method, demonstrating its effectiveness in real-world scenarios.

Bioadhesive Gauze Embedded with Chitosan-Butein Bioconjugate: A Redox-Active pH Sensor Platform.

With the ever-growing global wound care market, demand for robust redox-active healthcare material is obvious for the construction of wearable sensor platforms. Surface reactive functional group-rich material like chitosan holds huge potential for electrochemical biosensor application. Herein, a metal-free redox-active chitosan-butein (CSB) bioconjugate is processed into epidermal bioadhesive electrode material useful for pH sensors promising toward wound site analysis. A two-electrode system devised for conducting carbon-reinforced silver chloride paste and CSB-modified carbon/silver chloride matrix was used as a reference and working electrodes, respectively. Dimensions of working and reference electrodes (4 mm) were designed by 2D cutter plotter-assisted stenciling. The cross-sectional topology of the constructed adhesive CSB-sensor platform exhibits an average surface thickness of 183 ± 2 µm. Cyclic voltammetric analysis revealed the inherent 2e-/2H+ transfer attributed to the catechol OH groups of graft polymerized CSB modified on adhesive gauze. As-fabricated modified electrode substrates exhibit distinguishable potential differences with respect to electrolytes of varied pH (between 5 to 9), promising for wound site analysis.

Towards the development of reagent-free and reusable electrochemical aptamer-based cortisol sensor.

Continuous monitoring of stress through detecting specific biochemical markers such as cortisol plays a crucial role in the early detection of various diseases. Electrochemical aptamer sensor involving binding induced conformational change allows the continuous measurement of biomarkers. A reagent-less aptamer-based biosensing platform that allows a continuous and real-time cortisol measurement is developed in this context. The aptamer is conjugated with methylene blue, which acts as a redox reporter to probe the cortisol binding quantitatively on the sensor surface. The cortisol specific aptamers were chemically modified with amine and thiol functional groups to facilitate redox reporter conjugation and attachment of aptamer to a gold electrode, respectively. The sensor achieves a clinically meaningful cortisol concentration ranging from 0.05 ng/mL to 100 ng/mL and provides good selectivity when challenged with structurally similar targets. The reagent-less measurement capability was also demonstrated using an undiluted human serum. The newly developed cortisol sensor can enable the systemic cortisol measurement for providing insights into cortisol related clinical conditions and medical treatments.