Composite of a Stabilizer-Free Trimetallic Prussian Blue Analogue (PBA) and Polyaniline (PANI) on 3D Porous Nickel Foam for the Detection of Nitrofurantoin in Biological Fluids.

Herein, a facile and highly effective nonenzymatic electrochemical sensing system is designed for the detection of the antibacterial drug nitrofurantoin (NFT). This electrocatalyst is a combination of a trimetallic Prussian blue analogue and conductive polyaniline coated onto a three-dimensional porous nickel foam substrate. A comprehensive set of physicochemical analyses have verified the successful synthesis. The fabricated electrochemical sensor exhibits an impressively low limit of detection (0.096 nM) and quantification (0.338 nM, S/N = 3.3), coupled with a wide linear range spanning from 0.1 nM to 5 mM and a sensitivity of 13.9 µA nM-1 cm-2. This excellent performance is attributed to the collaborative effects of conducting properties of polyaniline (PANI) and the remarkable redox behavior of the Prussian blue analogue (PBA). When both are integrated into the nickel foam, they create a significantly enlarged surface area with numerous catalytic active sites, enhancing the sensor's efficiency. The sensor demonstrates a high degree of specificity for NFT, while effectively minimizing responses to potential interferences such as flutamide, ascorbic acid, glucose, dopamine, uric acid, and nitrophenol, even when present in 2-3-fold higher concentrations. Moreover, to validate its practical utility, the sensor underwent real sample analysis using synthetic urine, achieving outstanding recovery rates of 118 and 101%.

Nickel-cobalt metal-organic frameworks based flexible hydrogel as a wearable contact lens for electrochemical sensing of urea in tear samples.

A flexible, wearable, non-invasive contact lens sensor utilizing nickel-cobalt metal-organic framework (Ni-Co-MOF) based hydrogel is introduced for urea monitoring in tear samples. The synthesized Ni-Co-MOF hydrogel exhibits a porous structure with interconnected voids, as visualized by Scanning Electron Microscopy (SEM). Detailed structural and vibrational properties of the material were characterized using X-ray Diffraction (XRD), Fourier Transform Infrared (FTIR) spectroscopy, and Raman spectroscopy. The developed Ni-Co-MOF hydrogel sensor showcases a detection limit of 0.445 mM for urea within a linear range of 0.5-70 mM. Notably, it demonstrates exceptional selectivity, effectively distinguishing against interfering species like UA, AA, glucose, dopamine, Cl-, K+, Na+, Ca2+, and IgG. The enhanced electrocatalytic performance of the Ni-Co-MOF hydrogel electrode is attributed to the presence of Ni and Co, fostering Ni2+ oxidation on the surface and forming a Co2+ complex that acts as a catalyst for urea oxidation. The fabricated sensor exhibits successful detection and retrieval of urea in simulated tear samples, showcasing promising potential for bioanalytical applications. The binder-free, non-toxic nature of the Ni-Co-MOF hydrogel sensor presents exciting avenues for future utilization in non-enzymatic electrochemical sensing, including applications in wearable devices, point-of-care diagnostics, and personalized healthcare monitoring.

Binary Ni-Fe layered double hydroxide on flexible nickel foam for the wide-range voltammetric detection of fibrinogen in simulated body fluid.

Fibrinogen, a circulating glycoprotein in the blood, is a potential biomarker of various health conditions. This work reports a flexible electrochemical sensor based on Ni-Fe layered double hydroxide (Ni-Fe LDH) coated on Nickel foam (Ni-Fe LDH/NF) to detect fibrinogen in simulated human body fluid (or blood plasma). The nanoflakes like morphology and hexagonal crystal structure of LDH, synthesized via urea hydrolysis assisted precipitation technique, are revealed by scanning electron microscopy (SEM) and powder x-ray diffraction (PXRD) techniques, respectively. The fabricated sensor exhibits linearity in a wide dynamic range covering the physiological concentration, from 1 ng ml-1to 10 mg ml-1, with a sensitivity of 0.0914 mA (ng/ml)-1(cm)-2. This LDH-based sensor is found to have a limit of detection (LOD) of 0.097 ng ml-1and a limit of quantification (LOQ) of 0.294 ng ml-1(S/N = 3.3). The higher selectivity of the sensor towards fibrinogen protein is verified in the presence of various interfering analytes such as dopamine, epinephrine, serotonin, glucose, potassium, chloride, and magnesium ions. The sensor is successful in the trace-level detection of fibrinogen in simulated body fluid with excellent recovery percentages ranging from 99.5% to 102.5%, proving the synergetic combination of 2D Ni-Fe layered double hydroxide and 3D nickel foam as a promising platform for electrochemical sensing that has immense potential in clinical applications.

ZnO nanoparticles-copper metal-organic framework composite on 3D porous nickel foam: a novel electrochemical sensing platform to detect serotonin in blood serum.

Herein, we report a simple non-enzymatic electrochemical sensor for the detection of serotonin (5-HT) in blood serum using ZnO oxide nanoparticles-copper metal-organic framework (MOF) composite on 3D porous nickel foam, namely, ZnO-Cu MOF/NF. The x-ray diffraction analysis reveals the crystalline nature of synthesized Cu MOF and Wurtzite structure of ZnO nanoparticles, whereas SEM characterization confirms the high surface area of the composite nanostructures. Differential pulse voltammetry analysis under optimal conditions yields a wide linear detection range of 1 ng ml-1to 1 mg ml-1to 5-HT concentrations and a LOD (signal to noise ratio = 3.3) of 0.49 ng ml-1, which is well below the lowest physiological concentration of 5-HT. The sensitivity of the fabricated sensor is found to be 0.0606 mA ng-1ml-1.cm2,and it exhibited remarkable selectivity towards serotonin in the presence of various interferants, including dopamine and AA, which coexist in the real biological matrix. Further, successful determination of 5-HT is achieved in the simulated blood serum sample with a good recovery percentage from ∼102.5% to ∼99.25%. The synergistic combination of the excellent electrocatalytic properties and surface area of the constituent nanomaterials proves the overall efficacy of this novel platform and shows immense potential to be used in developing versatile electrochemical sensors.