ABSTRACT
The factors influencing the appearance of toxicity in samples of synthetic montmorillonite with a systematically changing chemical composition Nax(Al, Mg)2-3Si4O10(OH)2 nH2O, which are potentially important for their use in medicine as drug carriers, targeted drug delivery systems, entero- and hemosorbents have been studied. Samples synthesized under hydrothermal conditions had the morphology of nanolayers self-organized into the nanosponge structures. The effect of the aluminum content, particle sizes, porosity, and ζ-potential of the samples on their toxicity was studied. The cytotoxic effect of the samples on eukaryotic cells Ea. hy 926 was determined using the MTT assay. The hemolytic activity of the samples in the wide concentration range in relation to human erythrocytes was also estimated. It has been established that the toxicity of aluminosilicate nanoparticles can be significantly reduced by correctly selecting their synthesis conditions and chemical composition, which opens up the opportunities for their use in medicine.
ABSTRACT
Porous glasses (PGs) obtained from sodium borosilicate (NBS) phase-separated glasses via leaching are promising inorganic membranes. Introducing Fe2O3 into NBS glasses imparts ferrimagnetic properties due to magnetite crystallization. Leaching of such glasses leads to the formation of magnetic PGs with interesting electro-surface characteristics. This work aimed to investigate the process of obtaining magnetite-containing PGs from NBS glasses depending on silica content, using XRPD and Raman spectroscopy, studying the PG membranes' structural characteristics and their sorption properties with respect to methylene blue (MB). Obtained PGs were characterized by a polymodal distribution of mesopores and a small number of micropores with specific surface area values of 32-135 m2/g and an average mesopore diameter of 5-41 nm. The kinetic data were analyzed using pseudo-first-order, pseudo-second-order, and intra-particle diffusion equations. The equilibrium isotherms were fitted with Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich models. MB adsorption was found to be a complex process. The glass with the highest specific surface area demonstrated the maximum sorption capacity (10.5 mg/g). The pore size of PGs allowed them to be considered potential novel magnetic membranes for ultrafiltration.
ABSTRACT
A comparative study of the properties of aluminosilicates of the kaolinite (Al2Si2O5(OH)4ânH2O) group with different particles morphology has been carried out. Under conditions of directed hydrothermal synthesis, kaolinite nanoparticles with spherical, sponge, and platy morphologies were obtained. Raw nanotubular halloysite was used as particles with tubular morphology. The samples were studied by X-ray diffraction, SEM, solid-state NMR, low-temperature nitrogen adsorption, and the dependence of the zeta potential of the samples on the pH of the medium was defined. The sorption capacity with respect to cationic dye methylene blue in aqueous solutions was studied. It was found that sorption capacity depends on particles morphology and decreases in the series spheres-sponges-tubes-plates. The Langmuir, Freundlich, and Temkin models describe experimental methylene blue adsorption isotherms on aluminosilicates of the kaolinite subgroup with different particles morphology. To process the kinetic data, pseudo-first order and pseudo-second order were used. For the first time, studies of the dependence of hemolytic activity and cytotoxicity of aluminosilicate nanoparticles on their morphology were carried out. It was found that aluminosilicate nanosponges and spherical particles are not toxic to human erythrocytes and do not cause their destruction at sample concentrations from 0.1 to 1 mg/g. Based on the results of the MTT test, the concentration value that causes 50% inhibition of cell population growth (IC50, mg/mL) was calculated. For nanotubes, this value turned out to be the smallest-0.33 mg/mL. For samples with platy, spherical and nanosponge morphology, the IC50 values were 1.55, 2.68, and 4.69 mg/mL, respectively.
