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In this study, zinc oxide nanoparticles (ZnO‐NPs) are synthesized and combined with chitosan (Cs) to create Cs/ZnO‐NPs nanomicelles, aiming to investigate their potential as a novel cancer treatment. The ZnO‐NPs are produced through a sintering process at temperatures ranging from 300 to 700 °C. The most effective nanoparticles are obtained at 600 °C, as determined by X‐ray diffraction (XRD) and Fourier‐transform infrared spectroscopy (FTIR) analyses, which confirmed their crystallinity and purity. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) are employed to characterize the size and shape of the nanoparticles, revealing predominantly spherical and hexagonal structures with stable dimensions. The cytotoxic effects of the Cs/ZnO‐NPs are evaluated against various cancer cell types. The results show that at a concentration of 125 µg mL−1, the Cs/ZnO‐NPs demonstrate significantly higher cancer cell toxicity compared to ZnO‐NPs alone, while remaining non‐toxic to normal cells. This indicates that Cs/ZnO‐NPs have a superior ability to selectively target cancer cells. These findings suggest that Cs/ZnO‐NPs nanomicelles hold promise as an effective and safe nanotherapeutic approach in the realm of cancer treatment, meriting further exploration for clinical applications. [ABSTRACT FROM AUTHOR]

The purpose of this study was to investigate the effect of OH concentration on the size of Fe3O4 nanoparticles (Fe3O4-NPs). Fe3O4-NPs with different cubic nanocrystal structure and percentage Fe3O4 content were successfully prepared, by use of the chemical co-precipitation method, on the exterior surface of talc, as solid substrate, by an environmentally friendly process. Ferric chloride, ferrous chloride, and sodium hydroxide were used as iron oxide precursors and reducing agent. The results showed that the morphology of the Fe3O4-NPs can be adjusted by changing the reaction conditions, for example volume of reducing agent and concentration of iron salts. Different size, dispersal, and the magnetic properties were obtained by changing the concentration of iron salts and NaOH. The products were characterized by powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and Fourier-transform infrared spectroscopy. The reaction was conducted in a non-oxidizing, oxygen-free environment. Because the interlamellar spacing of the talc was almost unchanged (ds = 0.94-0.87 nm), the Fe3O4-NPs were formed on the exterior surface of the talc. The average diameter of the Fe3O4-NCs could be varied from 6.62-8.13 nm in adjusting the concentration of NaOH. The size of the nanoparticles decreased as the amount of reducing agent was increased. These talc-Fe3O4nanocomposites (talc-Fe3O4-NCs) may have potential applications in the chemical and biological industries. [ABSTRACT FROM AUTHOR]

Small sized magnetite iron oxide nanoparticles (Fe3O4-NPs) with were successfully synthesized on the surface of rice straw using the quick precipitation method in the absence of any heat treatment. Ferric chloride (FeCl3.6H2O), ferrous chloride (FeCl2.4H2O), sodium hydroxide (NaOH) and urea (CH4N2O) were used as Fe3O4-NPs precursors, reducing agent and stabilizer, respectively. The rice straw fibers were dispersed in deionized water, and then urea was added to the suspension, after that ferric and ferrous chloride were added to this mixture and stirred. After the absorption of iron ions on the surface layer of the fibers, the ions were reduced with NaOH by a quick precipitation method. The reaction was carried out under N2 gas. The mean diameter and standard deviation of metal oxide NPs synthesized in rice straw/Fe3O4 nanocomposites (NCs) were 9.93 ± 2.42 nm. The prepared rice straw/Fe3O4-NCS were characterized using powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive X-ray fluorescence (EDXF) and Fourier transforms infrared spectroscopy (FT-IR). The rice straw/Fe3O4-NCs prepared by this method have magnetic properties. [ABSTRACT FROM AUTHOR]

This paper presents the green synthesis of silver nanoparticles (Ag NPs) in aqueous medium. This method was performed by reducing AgNO3 in different stirring times of reaction at a moderate temperature using green agents, chitosan (Cts) and polyethylene glycol (PEG). In this work, silver nitrate (AgNO3) was used as the silver precursor while Cts and PEG were used as the solid support and polymeric stabilizer. The properties of Ag/Cts/PEG nanocomposites (NCs) were studied under different stirring times of reaction. The developed Ag/Cts/PEG NCs were then characterized by the ultraviolet-visible (UV-Vis) spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectroscopy. [ABSTRACT FROM AUTHOR]

A green quick precipitation method was successfully used for synthesis of magnetic iron oxide nanoparticles (Fe3O4-NPs) on the surface of sodium/potassium type zeolite. Ferric chloride, ferrous chloride and sodium hydroxide aqueous solutions were used in the synthesis and coating of the Fe3O4-NPs on the surface of the zeolite to produce the zeolite/magnetic iron oxide nanocomposite (zeolite/Fe3O4 -NCs). The reaction was performed in aqueous suspension phase under the ambient condition as green chemistry method. Characterization with Fourier transforms infrared spectroscopy (FT-IR), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), energy dispersive X-ray fluorescence (EDXF) and transmission electron microscopy (TEM) confirmed the formation of Fe3O4-NPs with mean particle sizes of 3.55±1.02 nm on the surface of the zeolite. [ABSTRACT FROM AUTHOR]