New types of contactless luminescence nanothermometers, namely, LiAl₅O₈:Fe³⁺ and LiAl₅O₈:Fe³⁺, Nd³⁺ are presented for the first time, revealing the potential for applications in biological systems. The temperature-sensing capability of the nanocrystals was analyzed in wide range of temperature (−150 to 300 °C). The emission intensity of the Fe³⁺ ions is affected by the change in temperature, which induces quenching of the ⁴T₁ (⁴G) → ⁶A₁ (⁶S) Fe³⁺ transition situated in the 1st biological window. The highest relative sensitivity in the temperature range (0 to 50 °C) was found to be 0.82% °C (at 26 °C) for LiAl₅O₈: 0.05% Fe³⁺ nanoparticles that are characterized by long luminescent lifetime of 5.64 ms. In the range of low and high temperatures the S_max was calculated for LiAl₅O₈:0.5% Fe³⁺ to be 0.92% °C at −100 °C and for LiAl₅O₈:0.01% Fe³⁺ to be 0.79% °C at 150 °C. The cytotoxicity assessment carried out on the LiAl₅O₈:Fe³⁺ nanocrystals, demonstrated that they are biocompatible and may be utilized for in vivo temperature sensing. The ratiometric luminescent nanothermometer, LiAl₅O₈:Fe³⁺, Nd³⁺, which was used as a reference, possesses an S_max = 0.56%/°C at −80 °C, upon separate excitation of Fe³⁺ and Nd³⁺ ions using 266 nm and 808 nm light, respectively.

The aim of the study was to assess the effects of training on haematological and biochemical blood parameters as well as on the changes in body surface temperature in horses. In order to identify the predictive value of surface temperature measurements as a marker of animal's performance, their correlations with blood parameters were investigated. The study was carried out on nine horses divided into two groups: routinely ridden and never ridden. Infrared thermography was used to assess surface temperature changes before (BT) and just after training (JAT) on a treadmill. Seven regions of interest (ROIs) located on the neck, shoulder, elbow, back, chest, gluteus and quarter were analysed. The blood samples were taken BT, JAT and 30 min after training (30AT). Haematological parameters including white blood cells, lymphocytes (LYMs), monocytes (MONOs), granulocytes (GRAs), eosinophils (EOSs), haematocrit (HCT) and platelets (PLTs) as well as biochemical parameters such as glucose (GLUC), urea, Na⁺, K⁺ and Ca²⁺, and creatine phosphokinase (CPK) were analysed. Our results indicated a significant increase in surface temperature JAT (p=0.043) in the neck, shoulder, elbow, gluteus and quarter in routinely ridden horses. Significant changes in EOS (p=0.046) and HCT (p=0.043) in the case of the never-ridden and routinely ridden group, respectively, were found between the times of blood collection. In addition, there was a significant effect of the horse group and the time of blood collection on the CPK activity (p=0.025 to p=0.045) and urea concentrations (p=0.027 to p=0.045). In the routinely ridden horses, there were significant correlations between the changes in MONO (ρ=0.40), GRA ($\mathit{\rho }=-\mathrm{0.40}$ ), PLT ($\mathit{\rho }=-\mathrm{0.77}$ ), HCT ($\mathit{\rho }=-\mathrm{0.36}$ ), GLUC (ρ=0.56) and urea (ρ=0.56) and the total ROI temperature changes. Moreover, significant correlations between the changes in MONO ($\mathit{\rho }=-\mathrm{0.86})$ , EOS ($\mathit{\rho }=-\mathrm{0.65}$ ), GLUC (ρ=0.85), urea (ρ=0.85), Na⁺ (ρ=0.59) and K⁺ ($\mathit{\rho }=-\mathrm{0.85}$ ) and the total ROI temperature changes were found in never-ridden horses. Different changes in body surface temperature and blood parameters in routinely ridden and never-ridden horses could be associated with different conditioning and performance. A significantly higher surface temperature in routinely ridden horses, as well as the dynamics of changes in HCT, CPK and urea after training indicate better performance of these horses. Significant correlations between MONO, GLUC, and urea and a total ROI surface temperature as well as a negative correlation between MONO and the total ROI temperature in never-ridden horses indicated poor performance.

A HAP@β-TCP nanocomposite doped with Er ³⁺ /Yb ³⁺ ions was prepared and its cytotoxicity was tested on canine osteosarcoma and murine macrophage cells. Metronidazole release from the nanocomposite was studied and its up-conversion properties measured.

The increasing use of urinary catheters in healthcare, driven by an aging population and escalating antimicrobial resistance, presents both benefits and challenges. While they are essential to managing urinary retention and enabling precise urine output monitoring, their use significantly increases the risk of catheter-associated urinary tract infections (CAUTIs), the most common type of healthcare-associated infection. CAUTI risk is closely linked to the duration of catheterization and the formation of bacterial biofilms on catheter surfaces. These biofilms, often composed of polymicrobial communities encased in an extracellular matrix, promote persistent infections that are highly resistant to conventional antimicrobial therapies. Common CAUTI uropathogens include E. coli, E. faecalis, P. aeruginosa, P. mirabilis, K. pneumoniae, S. aureus, and Candida spp. The complexity and resilience of these biofilm-associated infections underscore the urgent need for innovative treatment strategies. Therefore, dynamic in vitro bladder infection models, which replicate physiological conditions such as urine flow and bladder voiding, have become valuable tools for studying microbial behavior, biofilm development, and therapeutic interventions under real clinical conditions. This review provides an overview of CAUTIs, explores the role of biofilms in sub-optimal responses to antimicrobial treatment and advances in model systems, and presents promising new approaches to combating these infections.