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Insufficient research has been conducted on the comprehensive detection of cetirizine dihydrochloride (CDH) in water bodies, while also overlooking the exploration of response time. Addressing these research gaps is crucial to enhance our understanding and detection capabilities of CDH in water. Consequently, the objective of this study was to develop an electrochemical sensor utilizing molybdenum trioxide (MoO3) nanointerfaced glassy carbon working electrode for the sensitive detection of CDH in water samples. The characterization of the MoO3 nanorods was conducted through morphological analysis using scanning electron microscopy, structural examination employing X-ray diffraction, and elemental analysis utilizing X-ray photoelectron spectroscopy. The integration of the MoO3 nanointerfaced sensor resulted in an enhanced electrochemical response during cyclic voltammetry, amperometry, and differential pulse voltammetry, attributed to its catalytic activity, electron transfer capability, and conductive nano-bioenvironment. The sensor demonstrated a detection potential of 0.927 V (vs Ag/AgCl) within a rapid response time of less than 50 s. Furthermore, the linear range of detection spanned from 10 to 70 µM, with a limit of detection as low as 194 ± 1.25 nM. The remarkable anti-interference properties of the MoO3 material further highlight the applicability of the fabricated sensor in real sample analysis. Successful validation of the developed sensor was achieved through the detection of CDH in water samples obtained from the Kaveri River. [ABSTRACT FROM AUTHOR]

In human blood serum, the concentration of magnesium ions typically ranges from 0.7 mM to 1.05 mM. However, exceeding the upper limit of 1.05 mM can lead to the condition known as hypermagnesemia. In this regard, a highly sensitive and selective electrochemical sensor for Mg(II) ion detection was successfully fabricated by immobilizing cerium oxide (CeO2) microcuboids, synthesized via microwave radiation method, onto the surface of glassy carbon electrode (GCE). Cyclic voltammetry studies revealed the exceptional electrocatalytic effect of CeO2 microcuboid-modified GC electrode, particularly in relation to the irreversible reduction signal of Mg(II). The microcuboid-like structure of CeO2 microparticles facilitated enhanced adsorption of Mg(II) ion ( Γ = 2.17 × 10 − 7 mol cm−2) and electron transfer ( k s = 8.94 s−1) between the adsorbed Mg(II) ions and GCE. A comprehensive analysis comparing the performance characteristics of amperometry, differential pulse voltammetry, cyclic voltammetry, and square wave voltammetry was conducted. The square wave voltammetry-based Mg(II) sensor exhibited remarkable sensitivity of 2.856 μA mM−1, encompassing a broad linear detection range of 0–3 mM. The detection and quantification limits were impressively low, with values of 19.84 and 66.06 μM, respectively. Remarkably, the developed electrode showed a rapid response time of less than 140 s. Multiple linear regression and partial least squares regression models were employed to establish a mathematical relationship between magnesium ion levels and electrochemical parameters. Notably, the proposed sensor exhibited excellent anti-interferent ability, repeatability, stability, and reproducibility, enabling the fabricated electrode to be used effectively for Mg(II) ion sensing in real-world samples. [ABSTRACT FROM AUTHOR]

Materials science and technology, with the advent of nanotechnology, has brought about innumerable nanomaterials and multi-functional materials, with intriguing yet profound properties, into the scientific realm. Even a minor functionalization of a nanomaterial brings about vast changes in its properties that could be potentially utilized in various applications, particularly for biological applications, as one of the primary needs at present is for point-of-care devices that can provide swifter, accurate, reliable, and reproducible results for the detection of various physiological conditions, or as elements that could increase the resolution of current bio-imaging procedures. In this regard, iron oxide nanoparticles, a major class of metal oxide nanoparticles, have been sweepingly synthesized, characterized, and studied for their essential properties; there are 14 polymorphs that have been reported so far in the literature. With such a background, this review's primary focus is the discussion of the different synthesis methods along with their structural, optical, magnetic, rheological and phase transformation properties. Subsequently, the review has been extrapolated to summarize the effective use of these nanoparticles as contrast agents in bio-imaging, therapeutic agents making use of its immune-toxicity and subsequent usage in hyperthermia for the treatment of cancer, electron transfer agents in copious electrochemical based enzymatic or non-enzymatic biosensors and bactericidal coatings over biomaterials to reduce the biofilm formation significantly. [ABSTRACT FROM AUTHOR]

Microwave irradiation technique provides a simple and quick synthesis route for nanomaterials at controlled experimental conditions. In this view, nanostructures of rGO, ZrO2, and rGO–ZrO2 composite were synthesized using microwave synthesis technique. Herein, we experimented the preparation of rGO using optimized conditions using convection mode at 373 K in a commercial microwave oven. Structural properties revealed the formation of mixed phases of the orthorhombic and rhombohedral crystal structure of ZrO2. The preferential plane orientation was found to be in c-axis (002) for rGO–ZrO2 nanocomposite, which revealed the predominance of rGO in the nanocomposite. Morphology of the prepared nanostructures exhibited agglomerated sheets, denser nanograins and randomly aggregated nanosheets for rGO, ZrO2, and mixed nanocomposite respectively. Room temperature gas sensing properties of the prepared nanostructures were investigated and reported. rGO showed responses of 5.3 and 5.2 towards 200 ppm of trimethylamine (TMA) and methanol. ZrO2 nanostructure showed a response of 35 towards 200 ppm of ammonia with response–recovery times of 91 and 6 s. [ABSTRACT FROM AUTHOR]

In recent times, the development of breath sensors for the detection of Diabetic Keto-Acidosis (DKA) has been gaining prominent importance in the field of health care and advanced diagnostics. Acetone is one of the prominent biomarkers in the exhaled breath of persons affected by DKA. In this background, nanostructured cobalt oxide sensing elements were fabricated using a spray pyrolysis technique at different deposition temperatures (473 to 773 K in steps of 100 K) towards the fabrication of an acetone sensor. The influence of deposition temperature on the various properties of the nanostructured cobalt oxide thin films was investigated. Formation of cubic spinel phase cobalt oxide was confirmed from the structural analysis. The shifting of plane orientation from (3 1 1) to (2 2 0) at 773 K deposition temperature revealed the migration of cobalt atoms to the highly favorable energy positions. Further, the downshifted peak absorption wavelength and upshifted PL profile at higher deposition temperature confirmed the migration of cobalt ions. The sensor fabricated at higher deposition temperature (773 K) showed a sensing response of 235 at room temperature towards 50 ppm of acetone. Also, the fabricated sensor showed a lower detection limit (LOD) of 1 ppm with the response-recovery times of 6 and 4 s, respectively. The LOD reported here is lower than the minimum threshold level (1.71 ppm) signifying the presence of DKA., Competing Interests: There is no conflict of interest to declare., (This journal is © The Royal Society of Chemistry.)