Nikolay M. Lyadov

The development of effective delivery systems for poorly soluble pharmaceuticals remains a critical challenge in modern pharmaceuticals. This study explores the use of lysozyme, a biopolymer with unique immunological and stabilizing properties, as a matrix for creating amorphous solid dispersions of nalidixic acid, a model hydrophobic antibiotic. By optimizing the composition using differential scanning calorimetry and X-ray powder diffractometry, a range of ratios of protein matrix and active pharmaceutical ingredient was determined in which amorphous solid dispersions are formed. Spray drying was used to produce microspherical particles suitable for inhalation therapy, resulting in particles predominantly 2–5 μm in size, suitable for alveolar deposition. This work demonstrates the potential of protein carriers such as lysozyme not only to enhance solubility and bioavailability but also to provide a synergistic therapeutic effect. The developed strategy for creating a dosage form is promising for improving the pulmonary delivery of other poorly water-soluble drugs while simultaneously reducing the required doses and minimizing side effects.

Obtaining amorphous forms of drugs is one of the ways to increase bioavailability. This is especially important for active pharmaceutical ingredients belonging to class II and IV according to the biopharmaceutical classification. These compounds include the currently widely used fluoroquinolone antibiotics. They have low solubility in water and are therefore typically used as hydrochlorides. The presence of a strong acid and a charged active pharmaceutical ingredient in the drug increases solubility, but can also lead to additional side effects and decreased permeability. One way to improve the properties of active pharmaceutical ingredients is to convert them to amorphous form. In this study, an amorphous form of the fluoroquinolone antibiotic norfloxacin was obtained, its stability was determined, and its solubility was studied. It was shown that the resulting amorphous form has good temporal stability. The optimal models describing the cold crystallization process are the Nakamura and Sbirrazzuoli models. Despite the slower dissolution kinetics compared to the crystalline sample, the amorphous form shows higher equilibrium solubility values. These results can be used in pharmaceutical engineering to produce amorphous forms of active pharmaceutical ingredients and determine their stability.

In this work, we have studied the microstructure and unusual ferromagnetic behavior in epitaxial tin dioxide (SnO₂) films implanted with 40 keV Co⁺ ions to a high fluence of 1.0 × 10¹⁷ ions/cm² at room or elevated substrate temperatures. The aim was to comprehensively understand the interplay between cobalt implant distribution, crystal defects (such as oxygen vacancies), and magnetic properties of Co-implanted SnO₂ films, which have potential applications in spintronics. We have utilized scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometry (VSM), differential thermomagnetic analysis (DTMA), and ferromagnetic resonance (FMR) to investigate Co-implanted epitaxial SnO₂ films. The comprehensive experimental investigation shows that the Co ion implantation with high cobalt concentration induces significant changes in the microstructure of SnO₂ films, leading to the appearance of ferromagnetism with the Curie temperature significantly above the room temperature. We also established a strong influence of implantation temperature and subsequent high-temperature annealing in air or under vacuum on the magnetic properties of Co-implanted SnO₂ films. In addition, we report a strong chemical effect of ethanol on the FMR spectra. The obtained results are discussed within the model of two magnetic layers, with different concentrations and valence states of the implanted cobalt, and with a high content of oxygen vacancies.

Anion doping of tungsten trioxide by nitrogen is used to obtain electrochrome cathode materials, the spectral transmittance of which can be controlled by the doping level. A series of samples was synthesized by reactive magnetron sputtering of a metal tungsten target in a mixture of argon, nitrogen, and oxygen gases, the flow rate of the latter was varied at a constant pressure of the gas mixture. Warm-colored tungsten oxynitride films were prepared at higher doping levels with their morphology and elemental composition characterized using scanning electron microscopy, crystal structure described using X-ray diffraction and the valence state of constituents revealed with X-ray photoelectron spectroscopy techniques. Optical properties were measured by making use of transmission spectrophotometry and spectroscopic ellipsometry. These extensive experimental studies revealed an increase in absorption towards shorter wavelengths below the wavelength of 0.5 µm with an increase in the doping level. At the same time, it was found that with an increase in the doping level, partial reduction of the tungsten occurs, and the fraction of non-stoichiometric oxygen steadily increases to half of the total oxygen content. It is a common belief that the imperfection of the doped material facilitates the intercalation of the material by electrolyte ions.

In this work, we have studied microstructure and unusual ferromagnetic behavior in cobalt (Co)-implanted epitaxial tin dioxide (SnO2) films. The study was aimed to provide a comprehensive understanding of the interplay between cobalt implant distribution, crystal defects, such as oxygen vacancies, and magnetic properties in Co-implanted SnO2 films, which has potential applications in spintronics and memristor devices. The scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometry (VSM), differential thermo-magnetic analysis (DTMA), and ferromagnetic resonance (FMR) were employed for investigations of SnO2 films implanted with 40 keV Co+ ions at room or the elevated temperatures of substrate. The experimental data showed that the Co ion implantation with high fluence of 1.0 1017 ions/cm2 induces significant changes in the microstructure of SnO2 films, leading to the appearance of ferromagnetism with the Curie temperature significantly above room temperature. Strong influence of implantation temperature and subsequent high-temperature annealing in air or in vacuum on magnetic properties of Co-implanted SnO2 films were established. Moreover, the chemical effect of ethanol on FMR spectra were observed. The obtained results are discussed within the model of two magnetic layers with different concentration and valence states of the implanted cobalt and with high content of oxygen vacancies.

Anion doping of tungsten trioxide by nitrogen is used to obtain electrochrome cathode material, the spectral transmittance of which can be controlled by the doping level. A series of samples was synthesized by reactive magnetron sputtering of a metal tungsten target in a mixture of argon, nitrogen and oxygen gases. Warm-colored tungsten oxynitride films were prepared at higher doping levels and characterized using scanning electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy techniques. Optical properties were measured making use of transmission spectrophotometry and spectroscopic ellipsometry. These extensive experimental studies revealed an increase in absorption towards shorter wavelengths with increasing the doping level. At the same time, it was found that with increasing the doping level, the fraction of non-stoichiometric oxygen also steadily increases to half the total oxygen content. The imperfection of the doped material can stimulate its intercalation with electrolyte ions, accelerating the coloring/bleaching process and increasing the dynamical range between the dark and clear states, thus improving the consumer qualities of electrochemical materials and devices.

Magnetic nanoparticles embedded into semiconductors have current perspectives for use in semiconducting spintronics. In this work, 40 keV Fe⁺ ions were implanted in high fluences of (0.5 ÷ 1.5) × 10¹⁷ ion/cm² into an oxide semiconductor and single-crystalline TiO₂ plates of rutile structure with (100) or (001) face orientations. Microstructure, elemental-phase composition, and magnetic properties of the Fe-ion-implanted TiO₂ were studied by scanning and transmission electron microscopies (SEM and TEM), X-ray photoelectron (XPS) and Rutherford backscattering (RBS) spectroscopies, as well as vibrating-sample magnetometry (VSM). The high-fluence ion implantation results in the formation of magnetic nanoparticles of metallic iron beneath the irradiated surface of rutile. The induced ferromagnetism and observed two- or four-fold magnetic anisotropy are associated with the endotaxial growth of Fe nanoparticles oriented along the crystallographic axes of TiO₂.

Li₃V₂(PO₄)₃/Li₃PO₄ (LVPO/LPO) composites as cathodes for Li-ion batteries were synthesized by the hydrothermal method and subsequently annealed in an Ar atmosphere. The effect of Li₃PO₄ content on the crystal structure, morphology and the related magnetic and electrochemical properties of Li₃V₂(PO₄)₃/Li₃PO₄ composites, containing 7.5 wt% and 14 wt% of Li₃PO₄ (LVPO/LPO-7.5 and LVPO/LPO-14) was investigated. The microstructure and morphology of the obtained composites were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM); magnetic and electrochemical properties investigations were performed using the electron spin resonance and galvanostatic methods, respectively. It was shown that Li₃V₂(PO₄)₃/Li₃PO₄ composites exhibit a high discharge capacity, good cycle performance (105 and 120 mAh g⁻¹ for the 200th cycle at 1C for LVPO/LPO-7.5 and LVPO/LPO-14, respectively), and insignificant changes in the surface morphology after 200 lithiation/delithiation cycles. Our results demonstrate that the increase in Li₃PO₄ content led to a decrease in the Li stoichiometry and magnetic inhomogeneity in Li₃V₂(PO₄)₃ phase; thus, the improvement in the electrochemical performance of LVPO/LPO composites due to incorporation of Li₃PO₄ can be attributed to their chemical and magnetic inhomogeneity.