Publications by authors named "Mohammad Muaz"

This study provides a comprehensive analysis of a biofabricated nanomaterial derived from root extract, evaluating its structural, morphological, and optical properties for use in asymmetric supercapacitors. The nanomaterial comprises pristine ZnO nanoparticles (ZnO NPs) and a 1% Ag-doped ZnO nanocomposite (Ag@ZnO NC), synthesized through a green-assisted sol-gel autocombustion method. Employing techniques such as X-ray diffraction, ultraviolet-visible near-infrared, scanning electron microscopy-energy-dispersive X-rayspectroscopy, Fourier transform infrared spectroscopy, Raman spectroscopy, and transmission electron microscopy, the study confirms a hexagonal wurtzite structure and nanocrystallites with spherical and hexagonal shapes (30 nm).

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This work presents an innovative and environmentally friendly biological synthesis approach for producing α-FeO nanoparticles (NPs) and the successful synthesis of α-FeO/reduced graphene oxide (rGO) nanocomposites (NCs). This novel synthesis route utilizes freshly extracted albumin, serving as both a reducing agent and a stabilizing agent, rendering it eco-friendly, cost-effective, and sustainable. A combination of characterization techniques including X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, and field emission scanning electron microscopy (FE-SEM) was employed to predict and confirm the formation of the as-synthesized α-FeO NPs and α-FeO/rGO NCs.

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In order to quench the thirst for efficient energy storage devices, a novel praseodymium-based state-of-the-art three-dimensional metal-organic framework (MOF), {[Pr(pdc)]MeNH} (YK-1), has been synthesized by using a simple solvothermal method employing a readily available ligand. YK-1 was characterised by single-crystal XRD and crystallographic analysis. The electrochemical measurements of YK-1 show that it exhibits a specific capacitance of 363.

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The drug pharmacokinetics is affected upon binding with proteins, thus making drug-protein interactions crucial. This study investigated the interaction between enzalutamide and human major antiproteinase alpha-2-macroglobulin (αM) by using multi spectroscopic and calorimetric techniques. The spectroscopic techniques such as circular dichroism (CD), intrinsic fluorescence, and UV-visible absorption were used to determine the mechanism of enzalutamide-αM interaction.

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