This study investigated the influence of chemical reagent selection on the properties of ZnO nanoparticles synthesized using the microwave-assisted hydrothermal method to control the intensities of near-band-edge (NBE) and defect-related deep-level (DLE) emissions. Two zinc precursors—zinc nitrate and zinc chloride—along with three different precipitating agents (NaOH, KOH, and NH₄OH) were used. ZnO nanoparticles from the ZnCl₂ precursor exhibited two orders of magnitude higher NBE/DLE intensity ratio compared to those obtained from zinc nitrate characterized by a higher contribution from defect-related emissions. Chlorine ions in ZnO nanoparticles play a key role in passivating defects by forming V₀-Cl₂ complexes, quenching luminescence associated with oxygen vacancies (V₀). Thermal treatment in a nitrogen atmosphere enhanced defect-related luminescence, possibly due to chlorine atom diffusion. This study highlights a successful synthesis of ZnO nanoparticles with low defect-related luminescence (DLE) achieved via the microwave-assisted hydrothermal method, a result rarely reported in the literature. The results emphasize the importance of reagent selection in controlling the morphology and optical properties, especially the defect density of ZnO nanoparticles. Optimizing these properties is crucial for biomedical applications such as bioimaging, antibacterial treatments, and photocatalysis.

Iron plays an important role in various crucial processes in the body and its deficiency is considered currently as a serious health problem. Thus, iron supplementation strategies for both humans and animals need to be effective and safe. According to our previous studies, zinc-based nanoparticles provide safe, biodegradable, fast and efficient transport system of orally given substances to the tissues. In the current manuscript we present results of a study aimed at investigation of the ZnO nanoparticle-based Fe supplementation system (average size 100 × 250 nm). Nanostructures were orally (gavage) administered to adult mice. Animals were sacrificed at different time points with collection of blood and internal organs for analyses (tissue iron concentration, hepatic level of hepcidin, blood parameters, liver and spleen levels of ferritin, histopathology). Initial experiment was performed to compare the biological effect of doping type (Fe³⁺ doping vs. a mixture of Fe³⁺ and Fe²⁺). Then, the effect of acute/chronic exposure models was determined. The increase in ferritin, along with improved, crucial hematological parameters and lack of the influence on hepcidin expression indicated the chronic application of Fe^3+,2+ doped ZnO nanostructures to be the most effective among tested.

Sleep paralysis (SP), an REM parasomnia, can be characterized as one of the symptoms of narcolepsy. The SP phenomenon involves regaining meta-consciousness by the dreamer during REM, when the physiological atonia of skeletal muscles is accompanied by visual and auditory hallucinations that are perceived as vivid and distressing nightmares. Sensory impressions include personification of an unknown presence, strong chest pressure sensation, and intense fear resulting from subjective interaction with the unfolding nightmare. While the mechanism underlying skeletal muscle atonia is known, the physiology of hallucinations remains unclear. Their complex etiology involves interactions among various membrane receptor systems and neurotransmitters, which leads to altered neuronal functionality and disruptions in sensory perception. According to current knowledge, serotonergic activation of 5-hydroxytryptamine-receptor-2A (5-HT2A)-associated pathways plays a critical role in promoting hallucinogenesis during SP. Furthermore, they share similarities with psychedelic-substance-induced ones (i.e., LSD, psilocybin, and 2,5-dimethoxy-4-iodoamphetamine). These compounds also target the 5-HT2A receptor; however, their molecular mechanism varies from serotonin-induced ones. The current review discusses the intracellular signaling pathways responsible for promoting hallucinations in SP, highlighting the critical role of β-arrestin-2. We propose that the β-arrestin-2 signaling pathway does not directly induce hallucinations but creates a state of network susceptibility that facilitates their abrupt emergence in sensory areas. Understanding the molecular basis of serotonergic hallucinations and gaining better insight into 5-HT2A-receptor-dependent pathways may prove crucial in the treatment of multifactorial neuropsychiatric disorders associated with the dysfunctional activity of serotonin receptors.

This article addresses the issue of circular public procurement within the circular economy. The aim of the article is to investigate the relationship between awarding circular public procurements (CPPs) by local government units (LGUs) and the local context indicators, such as legally protected areas, level of income, expenditure or deficit per inhabitant, type of LGUs or model of LGUs management. The theoretical part approaches issues such as LGUs’ practice of awarding CPPs, and the problems associated with circular tenders’ criteria. The conducted empirical study revealed the potential of Polish LGUs for the circular economy, in the field of CPP. However, the results of the survey demonstrated that CPPs based on environmental, social, and economic award criteria, are a myth, not reality. LGUs have very strong purchasing power which may be used to support transformation toward a circular economy. The concluding part highlighted the need for minimum mandatory CPP awarding criteria.

With the spread of nanotechnology use in industry, exposure to nanomaterials is currently exponentially increasing. With reports indicating nanoparticles’ ability to pass through key biological barriers—gastrointestinal, lung, skin, blood-brain and the placenta barriers—the question of their safety, particularly the risks associated with embryonic development, arises. The aim of this article is to verify the impact of ZnO nanoparticles, which are commonly used and considered to be safe for adult organisms on the developing embryo. In the current study, the influence of the dose and shape of ZnO nanoparticles (oval vs. long) was evaluated in the chicken embryo model. The oxidative stress (superoxide dismutase (SOD)) activity, malondialdehyde (MDA) and carbonylated protein ((CP) levels), and gene expression changes (full genomic microarray study) were tested. We found that at both doses (10 µg/mL and 100 µg/mL, 100 µL into the air chamber) neither elongated nor oval ZnO nanoparticles changed in ovo mortality. Long ZnO nanoparticles had a lesser and more delayed impact on evaluated parameters, regardless of their higher in vitro toxicity. However, both nanoparticle forms induced changes in the oxidoreductive potential and affected expression of a significant number (1487 for oval and 548 for long ZnO nanoparticles) of identified genes during early embryo development.

The blood–brain barrier (BBB) is critical for central nervous system homeostasis, yet it is highly vulnerable to viral insults. While acute coronavirus infections are known to impair BBB integrity, the long-term impact of persistent infection on brain endothelial cells remains poorly understood. Using an in vitro BBB model, we examined the effects of a 12-week infection with the neurotropic murine coronavirus MHV-JHM. Structural and functional changes were assessed via fluorescein isothiocyanate (FITC)-dextran permeability assay, confocal imaging of mitochondria, actin cytoskeleton, reactive oxygen species (ROS), scanning electron microscopy (SEM) and RT-qPCR for viral RNA level. Long-term infection induced progressive mitochondrial fragmentation and sustained ROS overproduction. Permeability to 70 kDa dextran increased significantly at 48 h post-infection and exceeded control levels threefold by 168 h. SEM revealed gradual endothelial surface roughening, blebbing, and eventual monolayer collapse with extensive intercellular gaps by week 12. Our study demonstrates that long-term MHV-JHM infection profoundly alters brain endothelial cell structure and function, triggering a cascade of changes that culminate in the disintegration of the BBB model.