The review is devoted to the analysis of the compositional disordering potential of the crystal matrix of a scintillator to improve its scintillation parameters. Technological capabilities to complicate crystal matrices both in anionic and cationic sublattices of a variety of compounds are examined. The effects of the disorder at nano-level on the landscape at the bottom of the conduction band, which is adjacent to the band gap, have been discussed. The ways to control the composition of polycationic compounds when creating precursors, the role of disorder in the anionic sublattice in alkali halide compounds, a positive role of Gd based matrices on scintillation properties, and the control of the heterovalent state of the activator by creation of disorder in silicates have been considered as well. The benefits of introducing a 3D printing method, which is prospective for the engineering and production of scintillators at the nanoscale level, have been manifested.

Technological factors and processes contributing to the scintillation mechanism have been considered in quaternary garnet ceramics doped with Ce(Gd,Lu)₃Al₂Ga₃O₁₂. The super-stoichiometric additive of gadolinium in the material composition or its co-doping with a low concentration of Mg were found to be effective tools to suppress phosphorescence in the quaternary garnet, confirming that it is not an intrinsic property of the material. The Monte-Carlo simulation of electronic excitation transfer demonstrates that the hopping migration along the gadolinium sublattice plays an essential role in forming the scintillation kinetic parameters. Breaking the integrity of the gadolinium sublattice by substitution with heavier lutetium ions increases the role of self-trapped states in the excitation of Ce³⁺ ions, which ensures both an increase in the fraction of short ~20 ns and very long ~600 ns components in the scintillation kinetics.

Magnetic nanosystems (MNSs) consisting of magnetic iron oxide nanoparticles (IONPs) coated by human serum albumin (HSA), commonly used as a component of hybrid nanosystems for theranostics, were engineered and characterized. The HSA coating was obtained by means of adsorption and free radical modification of the protein molecules on the surface of IONPs exhibiting peroxidase-like activity. The generation of hydroxyl radicals in the reaction of IONPs with hydrogen peroxide was proven by the spin trap technique. The methods of dynamic light scattering (DLS) and electron magnetic resonance (EMR) were applied to confirm the stability of the coatings formed on the surface of the IONPs. The synthesized MNSs (d ~35 nm by DLS) were intraarterially administered in tumors implanted to rats in the dose range from 20 to 60 μg per animal and studied in vivo as a contrasting agent for computed tomography. The long-term (within 14 days of the experiment) presence of the MNSs in the tumor vascular bed was detected without immediate or delayed adverse reactions and significant systemic toxic effects during the observation period. The peroxidase-like activity of MNSs was proven by the colorimetric test with o-phenylenediamine (OPD) as a substrate. The potential of the synthesized MNSs to be used for theranostics, particularly, in oncology, was discussed.

Two series of (Gd, Y, Yb)₃Al₂Ga₃O₁₂ quintuple compounds with a garnet structure and solely doped with Ce and Tb were prepared in the form of ceramics by sintering in oxygen at 1600 °C for two hours and studied for the interaction of activator ions with ytterbium ions entering the matrix. It was shown that the photoluminescence and scintillation of Ce³⁺ ions are completely suppressed, predominantly by tunneling ionization through the charge transfer state (CTS) of the Ce⁴⁺-Yb²⁺ ions. The photoluminescence of Tb³⁺ ions is quenched in the presence of ytterbium, but not completely due to the poor resonance conditions of Tb³⁺ intraconfiguration transitions and the CTS of the single Yb³⁺ and the CTS of Ce⁴⁺-Yb²⁺ ions. The scintillation in the visible range of both Ce³⁺- and Tb³⁺-doped samples is intensely quenched as well, which indicates strong competition from Yb³⁺ ions to activators in interaction with the Gd substrate.