Mesoporous silica SBA-15 was prepared via sol-gel synthesis and functionalized with different types of organosilanes containing various organic functional groups: (3-aminopropyl)triethoxysilane (SBA-15-NH₂), (3-mercaptopropyl)triethoxysilane (SBA-15-SH), triethoxymethylsilane (SBA-15-CH₃), triethoxyphenylsilane (SBA-15-Ph), and (3-isocynatopropyl)triethoxysilane (SBA-15-NCO). The prepared materials were investigated as drug delivery systems for naproxen. As model drugs, naproxen acid (HNAP) and its sodium salt (NaNAP) were used. Mentioned medicaments belong to the group of non-steroidal anti-inflammatory drugs (NSAIDs). The prepared materials were characterized by different analytical methods such as transmission electron microscopy (TEM), infrared spectroscopy (IR), nitrogen adsorption/desorption analysis (N₂), thermogravimetric analysis (TG), ¹H, ¹³C and ²³Na solid-state nuclear magnetic resonance spectroscopy (¹H, ¹³C and ²³Na ss-NMR). The abovementioned analytical techniques confirmed the successful grafting of functional groups to the SBA-15 surface and the adsorption of drugs after the impregnation process. The BET area values decreased from 927 m² g⁻¹ for SBA-15 to 408 m² g⁻¹ for SBA-15-NCO. After drug encapsulation, a more significant decrease in surface area was observed due to the filling of pores with drug molecules, while the most significant decrease was observed for the SBA-15-NH₂ material (115 m² g⁻¹ for NaNAP and 101 m² g⁻¹ for HNAP). By combining TG and nitrogen adsorption results, the occurrence of functional groups and the affinity of drugs to the carriers’ surface were calculated. The dominant factor was the volume of functional groups and intermolecular interactions. The highest drug affinity values were observed for phenyl and amine-modified materials (SBA-15-Ph = 1.379 μmol m⁻² mmol⁻¹ for NaNAP, 1.761 μmol m⁻² mmol⁻¹ for HNAP and SBA-15-NH₂ = 1.343 μmol m⁻² mmol⁻¹ for NaNAP, 1.302 μmol m⁻² mmol⁻¹ for HNAP) due to the formation of hydrogen bonds and π-π interactions, respectively. Drug release properties and kinetic studies were performed at t = 37 °C (normal human body temperature) in different media with pH = 2 as simulated human gastric fluid and pH = 7.4, which simulated a physiological environment. Determination of drug release quantity was performed with UV-VIS spectroscopy. The surface polarity, pH and naproxen form influenced the total released amount of drug. In general, naproxen sodium salt has a higher solubility than its acid form, thus significantly affecting drug release from surface-modified SBA-15 materials. Different pH conditions involved surface protonation and formation/disruption of intermolecular interactions, influencing both the release rate and the total released amount of naproxen. Different kinetic models, zero-order, first-order, Higuchi and Hixson–Crowell models, were used to fit the drug release data. According to the obtained experimental results, the drug release rates and mechanisms were determined.

Three different magnetic beads consisting of Fe₃O₄ magnetic core, silica shell and organic ligand’s shell of 3-Mercaptopropyl-trimethoxysilane, Phenyl-3-aminopropyltrimethoxysilane and Trimethoxysily-propyl methacrylate were prepared with the aim to increase the surface active centres for DNA/RNA magnetic separation. The magnetic properties of prepared samples in powder form were studied by ZFC/FC magnetization and by field dependence of magnetization using SQUID magnetometry. The magnetic moment and the particles size distribution were calculated from experimental data by fitting of Langevin function. The properties of samples containing Trimethoxysilyl-propyl methacrylate in liquid form was compared with those measured on a commercially purchased kit designed for RT-PCR diagnostics. We have found that a detailed study of magnetic parameters serves as a very sensitive tool for the design of magnetic beads for PCR diagnostics, despite the fact that they contain a diamagnetic surface layer.

Magnetic-bead separation or purification serves as a technique for effective isolation of biomolecules. In presented work we prepared and characterized core-shell magnetic nanoparticle samples consisted of Fe₃O₄ core coated with SiO₂ shell. Samples were subsequently coated with ligands MPTMS (3-(mercaptopropyl)trimethoxysilane), CPTMS (3-(chloropropyl)trimethoxysilane) and MMSP (3-(trimethoxysilyl)propyl methacrylate) with aim to increase the number of active centers for specific binding with RNA. Such samples were further investigated for their magnetic properties, size, and morphology. Magnetic properties were studied in DC field up to 5 T in temperature range 5 – 300 K. Size and morphology were determined from SEM micrographs and elemental compositions of the samples were investigated using EDX analysis. Modification of nanoparticle surface with different ligands leads to modification of active centers on the SiO₂ surface on which the DNA and RNA molecules can be bounded. It also causes the change in magnetic and structural properties of nanoparticles.