This research examines the structural and magnetic properties of monodomain cobalt ferrite nanoparticles with the formula (Co_1−xFe_x)^A[Fe_2−xCo_x]^BO₄. The particles were synthesized using various methods, including coprecipitation (with and without ultrasonic assistance), coprecipitation followed by mechanochemical treatment, microemulsion, and microwave-assisted hydrothermal techniques. The resulting materials were extensively analyzed using X-ray diffraction (XRD) and magnetic measurements to investigate how different synthesis methods affect the structure and cation distribution in nanoscale CoFe₂O₄. For particles ranging from 15.8 to 19.0 nm in size, the coercivity showed a near-linear increase from 302 Oe to 1195 Oe as particle size increased. Saturation magnetization values fell between 62.6 emu g⁻¹ and 74.3 emu g⁻¹, primarily influenced by the inversion coefficient x (0.58–0.85). XRD analysis revealed that as the larger Co²⁺ cations migrate from B- to A-sites (decreasing x), the lattice constants and inter-cation hopping distances increase, while the average strength of super-exchange interactions decreases. This study establishes a connection between the magnetic properties of the synthesized samples and their structural features. Importantly, this research demonstrates that careful selection of the synthesis method can be used to control the magnetic properties of these nanoparticles.

Background/Objectives: Barium titanate (BaTiO₃)-based nanocarriers have emerged as versatile and promising platforms for targeted drug delivery, owing to their unique combination of biocompatibility, piezoelectric and ferroelectric properties, as well as responsiveness to external stimuli. These multifunctional ceramic nanoparticles can be precisely engineered to enable spatiotemporally controlled release of therapeutic agents, triggered by physical stimuli such as ultrasound, light, magnetic fields, temperature changes, and pH variations. Such an approach enhances treatment efficacy while reducing systemic side effects. Methods: This review provides a comprehensive overview of the latest advancements in the development and biomedical application of BaTiO₃-based nanocarriers. Special emphasis is placed on modern synthesis strategies, surface functionalization methods, and the integration of BaTiO₃ with other functional nanomaterials to create hybrid systems with improved therapeutic performance. Key challenges in clinical translation are also discussed, including biocompatibility assessment, biodistribution, and regulatory requirements. Conclusions: BaTiO₃-based nanocarriers show promise as materials well suited for advanced biomedical applications. The paper concludes with an outline of future research directions aimed at optimizing these advanced nanosystems for precision and personalized medicine, with applications in oncology, anti-infective therapy, and regenerative medicine.

Heterogeneous photocatalysis increasingly requires rapid polymer degradation tests relevant to aqueous conditions. In this study, a multi-technique approach was developed to monitor the early-stage photo-oxidation of polyethylene (PE) and polystyrene (PS) microplastics in an aqueous ZnO–TiO₂ suspension under combined ultraviolet A and ultraviolet B (UV-A/B) irradiation. The changes were analyzed by ATR-FTIR and Raman spectroscopy, DSC, and gravimetric measurements. For PE, the carbonyl index increased from 0.0189 to 0.1350 after 12 h, mass loss reached 16.98%, and crystallinity decreased from 32.05% to 25.36% after 8 h. The Raman spectra of PE showed band broadening and intensity redistribution, indicating increasing structural disorder. In contrast, PS showed weaker Raman changes, while FTIR revealed a non-monotonic carbonyl-index response, and DSC showed a 2.2 °C increase in Tg after 12 h. Gravimetric analysis also showed measurable mass loss in PS, reaching 18.62% after 12 h. The results demonstrate that the combined use of ATR-FTIR, Raman, DSC, and gravimetry enables reliable distinction between early oxidation, surface modification, and material erosion in photocatalytically treated microplastics.

Dicyclopentadiene (DCPD)–poly(methyl methacrylate) (PMMA) core–shell fibers were fabricated via coaxial electrospinning to develop a self-healing polymer composite. A PMMA shell containing a first-generation Grubbs catalyst was co-spun with a DCPD core at 0.5 mL h⁻¹ and 28 kV, yielding smooth, cylindrical fibers. The diameter range of nanofibers was 300–900 nm, with 95% below 800 nm, as confirmed by FESEM image analysis. FTIR spectroscopy monitored shell integrity via the PMMA C=O stretch and core polymerization via the trans-C=C bands. The high presence of the 970 cm⁻¹ band in the healed nanofiber mat and the minor appearance in the uncut core–shell mat demonstrated successful DCPD polymerization mostly where the intended damage was. The optical clarity of PMMA enabled the direct monitoring of healing progress via optical microscopy. The presented findings demonstrate that PMMA can retain a liquid active core and catalyst to form a polymer layer on a damaged site and could be used as a model material for other self-healing systems that require healing monitoring.