Search Results (57,922)

The modern multi-domain battlespace increasingly demands cost-effective, persistent platforms for Forward Air Control (Airborne) (FAC(A)) and Close Air Support (CAS) missions. While utilizing Commercial Derivative Aircraft (CDA) presents a viable alternative to high-maintenance military assets, the specific aerodynamic, ergonomic, and cognitive workload limitations encountered during the transition across the civil–military “airworthiness seam” remain a significantly underexplored gap in contemporary aerospace literature. To address this gap, a comprehensive empirical flight test campaign was executed on the LX7-135 turboprop to evaluate its tactical mission suitability. Employing the Cooper–Harper Handling Qualities Rating and Bedford Workload scales, and guided by military specifications (MIL-HDBK-516C, MIL-F-8785C), the study systematically assessed the aircraft’s pure performance, unaugmented flight dynamics, and human–machine interface during simulated combat scenarios, including dynamic 9-Line briefings and kinetic “Box Pattern” delivery profiles. Flight test data indicated 12 “SATISFACTORY” parameters, highlighting climb rates, extended endurance, and heavily damped short-period and Dutch roll modes optimal for target tracking. Conversely, the evaluation identified 4 “UNSATISFACTORY” and 10 “TOLERABLE” deficiencies—chiefly a single-door egress bottleneck, restricted stick clearance, degraded longitudinal static stability, and the absence of secure tactical communications. Although these constraints elevated pilot cognitive workload during multi-axis tasks, the LX7-135 demonstrates potential suitability for further development for the FAC(A) role, subject to the successful implementation and subsequent flight-test verification of the identified critical engineering modifications and specialized training syllabi. Full article

Ultraviolet B (UVB) radiation is a major environmental factor contributing to skin photoaging through excessive reactive oxygen species (ROS) generation, activation of stress-responsive signaling pathways, DNA damage, cellular senescence, and extracellular matrix (ECM) degradation. Mangiferin, a naturally occurring xanthone glucoside with potent antioxidant and anti-inflammatory properties, has attracted considerable interest as a potential photoprotective agent. The present study investigated the protective effects of mangiferin against UVB-induced photoaging in human dermal fibroblasts (HDFs). The effects of mangiferin on oxidative stress, RAGE/NF-κB/MAPK signaling, DNA damage, cellular senescence, and ECM degradation were evaluated. Mangiferin significantly suppressed UVB-induced ROS accumulation and attenuated activation of the RAGE/NF-κB/MAPK signaling cascade. Furthermore, mangiferin reduced γ-H2AX expression, indicating protection against UVB-mediated DNA damage, while decreasing p16, p21, and p53 expression and restoring LMNB1 levels. Mangiferin also inhibited MMP-2 and MMP-9 activities as well as collagenase, elastase, and hyaluronidase activities, suggesting preservation of ECM homeostasis. These findings demonstrate that mangiferin protects dermal fibroblasts against UVB-induced photoaging through suppression of oxidative stress, inhibition of RAGE/NF-κB/MAPK signaling, attenuation of DNA damage and cellular senescence, and preservation of ECM integrity, supporting its potential application in photoprotective and anti-photoaging dermocosmetic formulations. Full article

Background/Objectives: Plant-mediated silver nanoparticles (AgNPs) are promising components for oral biomaterials because of their antimicrobial potential; however, their biological behavior depends strongly on the phytochemical matrix, physicochemical characteristics, and exposure concentration. This study aimed to evaluate silver nanoparticles formulations synthesized using turmeric powder-derived Curcuma longa ethanolic and aqueous extracts, with emphasis on physicochemical characterization, antibacterial activity against oral-relevant Gram-positive bacteria, cytocompatibility toward human gingival fibroblasts (HGF-1), and acute in ovo vascular compatibility. Methods: AgCUR-EtOH NPs and AgCUR-H₂O NPs were synthesized using CUR-EtOH and CUR-H₂O extracts as reducing and stabilizing matrices. The resulting formulations were characterized by UV–visible spectroscopy (UV-Vis), dynamic light scattering (DLS), zeta-potential analysis, X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDX). Minimum inhibitory concentrations (MICs) and minimum bactericidal concentrations (MBCs) were determined against Streptococcus mutans, Streptococcus oralis, and Staphylococcus aureus. Cytocompatibility was evaluated in HGF-1 human gingival fibroblasts after 24 h exposure to 1–10 µg/mL using complementary viability, lysosomal, mitochondrial, and fluorescence-based assays. Acute vascular irritation was assessed using the hen’s egg test–chorioallantoic membrane (HET-CAM) assay. Results: Both formulations exhibited broad, polydisperse hydrodynamic distributions and negative apparent zeta potentials. AgCUR-H₂O NPs showed a lower Z-average diameter than AgCUR-EtOH NPs under their respective solvent-specific measurement conditions. XRD pattern revealed heterogeneous crystalline compositions dominated by residual AgNO₃, together with weaker contributions consistent with metallic Ag and a possible minor oxidized silver phase. FTIR spectra demonstrated extract-derived organic functional groups and prominent nitrate-associated bands. TEM/EDX confirmed Ag-containing nanostructures with approximate size ranges of 15–175 nm for AgCUR-EtOH NPs and 15–150 nm for AgCUR-H₂O NPs. S. mutans was the most susceptible microorganism, with MIC values of 9 and 7 µg/mL and MBC values of 88 and 62 µg/mL for AgCUR-EtOH NPs and AgCUR-H₂O NPs, respectively. AgCUR-H₂O NPs consistently showed lower MIC and MBC values against all tested strains, but also produced a more pronounced concentration-dependent reduction in HGF-1 viability. At 10 µg/mL, cell viability was 71.88% for AgCUR-EtOH NPs and 52.14% for AgCUR-H₂O NPs. Both formulations showed low acute irritation potential in ovo, with irritation scores of 1.06 and 0.69, respectively. Conclusions: The two CUR-AgNP formulations exhibited distinct physicochemical, antibacterial, and cellular response profiles under the tested conditions. At equivalent concentrations expressed as total dried formulation mass, AgCUR-H₂O NPs yielded lower MIC and MBC values against the tested bacterial strains, whereas AgCUR-EtOH NPs produced a less pronounced reduction in HGF-1 viability. Because the powders were not quantitatively normalized for total silver, extract-derived organic fraction, or residual precursor content, these differences cannot be attributed exclusively to nanoparticle properties or to the extraction solvent and should not be interpreted as evidence of the intrinsic superiority of either formulation. Both formulations showed low acute vascular irritation. Further quantitative compositional, silver-release, and biofilm assessments are required before incorporation into oral biomaterial platforms. Full article

mRNA plays a pivotal role in cellular processes of genetic information transfer, and post-transcriptional modifications of its nucleotides enable regulation of these processes with each particular mRNA. m5C methylation is a specific RNA modification that is rather common in tRNA, rRNA, lncRNA and other types of non-coding RNAs, whereas in mRNA it is found not very often. However, the functioning of m5C-methylated mRNAs differs from the non-methylated ones quite dramatically. Of the eight m5C RNA methyltransferases in humans, only two, NSUN2 and NSUN6, were found to be capable of modifying the main portion of cellular mRNAs. A deficiency of NSUN2 and NSUN6 causes global changes in the transcriptome and translatome, and a corruption of the NSUN2 gene in humans is associated with neurodegenerative diseases and intellectual disability. Despite intensive research of m5C mRNA methylation in recent years, many aspects of this phenomenon and its significance remain problematic and far from understood. In this review, we discuss the available information on mRNA methylome biogenesis, methods for its study and analysis, effects of m5C modification on mRNA life, and place it in the general context of cell biology, attempting to draw the biological relevance of m5C mRNA methylation. We highlight the main inconsistencies and difficulties that arise, analyze their possible causes, and propose potential directions for further research that could clarify the controversial issues and provide a link between the NSUN2 deficiency and neurodegenerative diseases. Full article

Coastal wetlands are important sinks for heavy metals, yet the linkage between vertical redistribution, quantitative source contributions, and ecological–health risk drivers remain insufficiently understood. This study collected the stratified sediment samples from three depth intervals (0–20, 20–40, and 40–60 cm) from 28 representative sites in the coastal wetlands of western Bohai Bay, and evaluated the spatial distribution, vertical variation, pollution status, potential sources, and ecological–human health risks of eight heavy metals (Cr, Ni, Cu, Zn, As, Cd, Hg, and Pb). The mean concentrations were below the Class I limits of the Marine Sediment Quality Standard. Most metals were close to or slightly below regional background values, whereas Cu and As showed mild enrichment and Cr was higher than values reported for Bohai Bay and Hangzhou Bay. Vertical profiles were generally homogeneous, with weak enrichment of specific metals, probably due to sediment resuspension, tidal disturbance, and bioturbation. Pollution assessment based on the geoaccumulation index (Igeo), Nemerow pollution index (P_N), and pollution load index (PLI) consistently indicated low contamination levels, with Hg and Pb as the main contributors to the regional pollution load. Source apportionment indicated that heavy metals were jointly influenced by lithogenic background (38.9%), atmospheric deposition (31.1%), and local anthropogenic activities (30.0%). Ecological risk assessment showed that the integrated risk index (RI) remained within the low-risk category, although Hg consistently fell within the moderate-risk range and Cd approached the moderate-risk threshold. Health risk assessment showed that both non-carcinogenic and carcinogenic risks were within acceptable limits for all receptor groups. Children had higher risks in core residential areas, whereas adults showed higher risks in non-core industrial–agricultural zones because of increased exposure frequency. The source–risk analysis indicates that non-carcinogenic risk is mainly associated with background-derived Cr, whereas carcinogenic risk is primarily linked to anthropogenic As inputs. These findings indicate that source contributions and risk contributions are not necessarily consistent, highlighting the need for source-oriented risk management in industrialized coastal wetlands. Full article

Background and Objectives: Baccharis dracunculifolia DC. (Asteraceae), the main botanical source of Brazilian green propolis, is recognized for its high content of bioactive secondary metabolites. Given this potential, this study aimed to characterize the chemical profile of the crude extract (CE) from the aerial parts of B. dracunculifolia and to investigate its anti-inflammatory, antiproliferative, antioxidant, and photoprotective properties. Predictive computational analyses were used to assist the interpretation of the experimental findings. Methods: The CE was obtained by dynamic maceration with ethanol and chemically characterized by UHPLC-MS/MS using external calibration curves. Anti-inflammatory activity was evaluated by inhibiting nitric oxide (NO) in RAW 264.7 macrophages, while cellular antioxidant activity (CAA) was determined in the same model. Antiproliferative activity was evaluated against the human tumor cell lines AGS, Caco-2, MCF-7, and NCI-H460, as well as non-tumor VERO cells. Additionally, antioxidant potential was investigated using classical colorimetric methods (DPPH, FRAP, and ABTS). The extract was also quantified for total phenolic and flavonoid content, as well as sun protection factor (SPF). Furthermore, complementary computational analyses included PASS prediction, SwissTargetPrediction, Gene Ontology enrichment using PANTHER, SwissADME profiling, and toxicity prediction with ProTox-III. Results: UHPLC-MS/MS analysis revealed a profile rich in flavonoids and phenolic acids and led to the identification of 14 compounds not previously reported in B. dracunculifolia according to the literature examined, notably the flavonoid morin and the phenylpropanoid coniferaldehyde detected at comparatively high concentrations (>600 µg/g). CE inhibited NO production (IC₅₀ = 62.00 µg/mL) suggesting anti-inflammatory activity, and reduced intracellular oxidation by 81% (at 2000 µg/mL) in RAW 264.7 macrophages. The extract showed total phenolic content (83.62 to 540.40 µg gallic acid equivalents/mg of CE) and high levels of flavonoids (472.00–515.00 µg quercetin equivalents/mg of CE), antioxidant activity in the DPPH assay (IC₅₀ = 0.86 mg/mL), and relevant photoprotective potential (SPF = 7.79–19.30). Antiproliferative activity was moderate to weak (GI₅₀ = 165.00–257.00 µg/mL). In silico analyses identified predicted activities, molecular targets, and enriched biological processes related to redox homeostasis, inflammation, apoptosis, and cellular responses to UV radiation, suggesting biological functions potentially associated with the identified metabolites. Conclusions: The crude extract of B. dracunculifolia demonstrated significant cellular anti-inflammatory and antioxidant activities, likely associated with its phenolic composition and the presence of metabolites reported in this study for the first time in this species, particularly morin and coniferaldehyde. These findings expand the phytochemical knowledge of B. dracunculifolia and reinforce its potential as a source of bioactive compounds for pharmaceutical, nutraceutical, and photoprotective applications. Full article

The mechanisms underlying neurodegenerative diseases (NDDs) involve multiple pathological processes, such as abnormal protein aggregation, oxidative stress, neuroinflammation, mitochondrial dysfunction, and the disruption of neurovascular unit homeostasis. The blood–brain barrier (BBB) restricts drug exposure in the brain, posing a significant challenge for central nervous system delivery and for improving therapeutic efficacy. In recent years, carbon dots derived from natural products (CDs) have emerged as candidate materials for brain delivery and theranostic applications due to their small size, modifiable surfaces, fluorescence-tracking capability, and potential neuroprotective activity. This narrative review summarizes their sources, physicochemical characteristics, biological basis, interactions with the BBB, delivery strategies, neuroprotective effects, and imaging applications. Current evidence suggests that these CDs can alleviate oxidative stress and inflammatory responses, influence abnormal protein aggregation, and support drug delivery and fluorescence tracking in certain cellular and animal models. However, BBB permeability, brain fluorescence signals, brain parenchymal exposure, and therapeutic efficacy represent distinct levels of evidence and should not be considered interchangeable. Future studies should focus on strengthening material standardization, ensuring batch-to-batch consistency, characterizing absorption, distribution, metabolism, and excretion (ADME), conducting long-term safety assessments, and validating using humanized BBB models. Full article

Flexible electromagnetic actuators have attracted considerable attention for applications in soft robotics, adaptive manipulation, and human–machine interaction due to their fast response, large deformation capability, and inherent compliance. However, the concurrent application of high actuation performance and long-term cyclic durability remains a major challenge, particularly for liquid metal (LM)-based soft systems, where interfacial instability between LM conductors and polymer substrates often leads to performance degradation. In this work, we report a fabrication strategy in which patterned eutectic gallium–indium (EGaIn) liquid metal circuits are directly written onto electrospun graphene oxide/thermoplastic polyurethane (GO/TPU) nanofiber membranes. The incorporation of graphene oxide significantly enhances interfacial adhesion through hydrogen bonding interactions between oxygen-containing functional groups in GO and the native Ga₂O₃ layer on the LM surface, while the electrospun fibrous architecture further improves mechanical interlocking and structural stability. As a result, the fabricated actuator exhibits robust electromechanical performance, achieving a maximum bending deformation of 90° under a driving current of 0.8 A and maintaining stable operation over 2000 actuation cycles with negligible performance degradation. To further demonstrate its practical functionality, a soft robotic gripper was constructed based on the optimized actuator configuration. The gripper enables the stable grasping and lifting of objects with a weight up to seven times its own mass, while maintaining safe and compliant interaction with fragile objects. This work provides a simple yet effective strategy to simultaneously enhance actuation efficiency, interfacial stability, and mechanical reliability in LM-based GO/TPU flexible electromagnetic actuator systems, offering promising potential for next-generation soft robotic applications. Full article

Smallholder dairy farms are central to rural livelihoods in Latin America, yet feeding strategies can shift environmental burdens across climate, land, and water dimensions. This study integrated cluster analysis and life cycle assessment to identify methane-related feeding typologies and assess their environmental trade-offs in smallholder dairy farms in the Mexican highlands. Twenty-nine farms from two dairy regions were classified by k-means clustering into two methane-emission-related farm typologies, which were subsequently characterized by their observed feeding profiles: conserved-forage-dominant (Cluster 1, n = 17) and green-forage-dominant (Cluster 2, n = 12). Their environmental performance was assessed with a cradle-to-farm gate life cycle assessment following ISO 14040/14044 and ReCiPe 2016 Midpoint across 18 impact categories. Feed production and ration supply were the main hotspots, contributing 72 to 100% of the total impacts. Global warming potential averaged 2.29 and 2.47 kg CO₂-eq per kg of raw milk in Clusters 1 and 2, respectively. Within the study sample, exploratory comparisons indicated higher marine eutrophication and land use in Cluster 1, whereas Cluster 2 showed higher fine particulate matter formation, terrestrial acidification, terrestrial ecotoxicity, and human carcinogenic toxicity (nominal p < 0.05). These potential trade-offs require validation in larger cohorts and with more geographically representative inventories. These findings show that similar milk outputs can arise from distinct feeding pathways with different environmental trade-offs and that greater reliance on fresh forage does not necessarily imply a more favorable environmental profile. Cluster-based characterization offers a practical basis for improving feed sourcing and ration design in dairy systems facing resource constraints. Full article

Lead (Pb²⁺) pollution poses a severe threat to the ecological environment and human health due to its high toxicity, bioaccumulation, and refractory nature. Traditional treatment technologies for lead-contaminated wastewater, such as chemical precipitation, ion exchange, and membrane separation, often face limitations, including secondary pollution, high costs, and high energy consumption. In contrast, adsorption has emerged as a promising alternative technology with advantages such as a simple process, high efficiency at low concentrations, and renewability. Biomass-based hydrogels and their composite systems, as novel green adsorbent materials, combine the abundant functional groups of natural biomass with the structural stability, high porosity, and recoverability of hydrogels through a three-dimensional cross-linked network, offering unique advantages for lead ion adsorption. Depending on their composition, these systems range from fully biodegradable pure biopolymer networks to partly biodegradable or biomass-containing composites incorporating inorganic, carbon-based, or metal–organic framework (MOF) materials. This paper systematically reviews the latest research progress on cellulose, lignin, sodium alginate, chitosan, starch-based hydrogels, and their composite systems for lead (Pb²⁺) adsorption. First, the structural characteristics, cross-linking mechanisms, and functional modification strategies of various biomass hydrogels are introduced. Then, the adsorption mechanisms of Pb²⁺, including multiple modes of action such as coordination complexation, ion exchange, electrostatic interaction, and physical adsorption, are systematically analyzed. The adsorption performance of different material systems is compared in detail. The regeneration and recycling performance, as well as the potential practical applications, of the materials are evaluated. On this basis, the main challenges in current research are summarised: balancing adsorption capacity and mechanical strength, achieving selective adsorption in actual wastewater, improving regeneration efficiency, and optimizing costs. In addition, future development directions for biomass hydrogel adsorbent materials are discussed, including the design of multi-functional composite materials, the development of intelligent, responsive hydrogels, engineering-scale-up, and life-cycle assessment. This review aims to provide a theoretical framework and technical roadmap for the rational design of high-performance, sustainable hydrogel adsorbents and to promote their engineering application for the treatment of lead-contaminated wastewater. Full article

Background: Blood-accessible biomarkers may support future personalization of prostate cancer radiotherapy, but their interpretation depends on sampling timing relative to radiotherapy, androgen deprivation therapy, and post-treatment recovery. We mapped clinical evidence for selected biomarker domains beyond prostate-specific antigen: γ-H2AX/DNA damage response, IL-6/inflammatory mediators, testosterone/endocrine recovery and a prespecified galectin-1/3 immune–stromal domain evaluated as a potential evidence gap. Methods: We conducted a PRISMA-ScR scoping review of PubMed, Scopus, and Web of Science searched on 7 January 2026. Eligible original human studies evaluated soluble serum/plasma analytes or peripheral blood cell-based assays in prostate RT pathways. Data were charted by biomarker domain, treatment context, RT modality/fractionation, assay reporting, sampling schedule, and endpoint linkage. Results: Of 3499 records, 45 studies were included. No eligible study reported repeated circulating galectin-1/3 kinetics anchored to prostate radiotherapy, identifying a distinct clinical evidence gap. The remaining evidence was dominated by testosterone studies (n = 28), followed by IL-6/inflammatory mediators (n = 12) and γ-H2AX/DDR (n = 5). Testosterone studies were mapped as separate RT-only endocrine kinetics and ADT-anchored recovery streams. IL-6 studies mainly used during-RT or early post-RT sampling and linked trajectories to acute toxicity, fatigue, symptoms or inflammatory phenotypes; no included study directly validated serial IL-6/inflammatory trajectories against biochemical control, metastasis-free survival, or overall survival. γ-H2AX studies were characterized by ultra-acute, fraction-anchored sampling. Across domains, baseline definition and sampling timing limited interpretability more than assay platform alone. Conclusions: Evidence maturity was unequal across the selected domains. Testosterone provided the comparatively more developed longitudinal clinical literature, whereas IL-6/inflammatory mediators remained exploratory and were linked mainly to acute toxicity, fatigue, symptoms, and inflammatory phenotypes. γ-H2AX remained predominantly a translational and biodosimetry-oriented marker, while galectin-1/3 represented a hypothesis-generating clinical evidence gap. None of these biomarkers currently supports routine biomarker-guided prostate RT personalization. Future biomarker-embedded studies may benefit from domain-specific sampling considerations, explicit RT/systemic-therapy context stratification, standardized assay reporting, and clinically relevant endpoints. Full article

Background/Objectives: The chemokine receptor CXCR4 plays a pivotal role in tumor progression, metastasis, and therapy resistance and is frequently overexpressed in hematologic malignancies, including multiple myeloma and lymphoma. This study investigates a CXCR4-targeted theranostic platform comprising a PET imaging agent and two therapeutic radioconjugates derived from the high-affinity CXCR4 antagonist LY2510924. Methods: The PET tracer [¹⁸F]AlF-NOTA-SC and therapeutic radioconjugates [¹⁷⁷Lu]Lu-BL02 and [¹⁶¹Tb]Tb-BL02 were synthesized and evaluated. Radiolabeling efficiency, molar activity, and in vitro binding affinity were assessed. Specificity and uptake were evaluated in CXCR4-expressing U87.CD4.CXCR4 and MM.1S cells, with cytotoxic potential being analyzed via clonogenic survival assays. In vivo biodistribution and pharmacokinetics were evaluated in MM.1S xenograft mouse models, supported by longitudinal SPECT imaging. Results: All radioconjugates were obtained with high radiochemical purity (>98%). The constructs showed nanomolar affinity for human CXCR4; in vitro assays confirmed specific uptake in CXCR4-positive cells, and both therapeutic agents demonstrated dose-dependent cytotoxicity. In vivo, all compounds displayed comparable tumor uptake with low off-target accumulation. Co-injection studies confirmed consistent pharmacokinetics across agents, while SPECT/CT imaging demonstrated gradual tumor clearance of [¹⁷⁷Lu]Lu-BL02 over seven days. Conclusions: The radiopharmaceutical trio [¹⁸F]AlF-NOTA-SC, [¹⁷⁷Lu]Lu-BL02, and [¹⁶¹Tb]Tb-BL02 demonstrates the feasibility of a CXCR4-targeted theranostic approach for imaging and treating hematologic malignancies. The observed tumor washout highlights the need for further structural optimization to enhance tumor retention and therapeutic efficacy, providing a clear direction for future development toward clinical translation. Full article

Glyphosate, the world’s most widely used herbicide, is of growing concern in both human and veterinary medicine because livestock, companion, and working animals may be chronically exposed through feed, water, and grazing on treated land. This study evaluates the protective effects of vitamin E (α-tocopherol acetate) against chronic glyphosate-induced hepatotoxicity, multi-organ histopathological damage, and disturbances of systemic redox balance in male Wistar rats. Fifty-six rats were allocated to six groups: control, low-dose glyphosate (LG, 560 mg/kg/day), high-dose glyphosate (HG, 1120 mg/kg/day), LG + vitamin E, HG + vitamin E, and vitamin E alone. Treatments were administered by oral gavage for 30 days at equalised dosing volumes. Serum oxidant/antioxidant markers—total oxidant status (TOS), total antioxidant status (TAS) and the oxidative stress index (OSI)—hepatic enzymes (AST, ALT, ALP, LDH), renal markers (urea, creatinine) and cardiac marker creatine kinase-MB (CK-MB) were measured; liver, lung, kidney, testis and heart were examined histopathologically. Glyphosate produced dose-dependent hepatocellular enzyme elevations (AST, ALT) and progressive multi-organ histopathological injury. Contrary to expectation, serum TOS and OSI did not increase in the glyphosate-only groups but were instead lower than in controls, accompanied by a compensatory rise in TAS—indicating that circulating oxidant markers may underestimate tissue-level oxidative injury at this exposure duration. Vitamin E co-administration markedly enhanced TAS, lowered TOS relative to the corresponding glyphosate group (HG + VitE vs. HG, p = 0.007), reduced OSI and substantially attenuated histopathological damage across all examined organs. Vitamin E thus mitigates glyphosate-induced tissue injury and improves systemic antioxidant capacity, supporting its potential as a protective dietary antioxidant in animals subject to chronic glyphosate exposure. Full article

Background: Glioblastoma (GBM) is the most aggressive primary brain tumour in adults and is characterised by poor prognosis and frequent resistance to temozolomide (TMZ)-based chemotherapy. Increasing evidence suggests that long non-coding RNAs (lncRNAs) contribute to GBM progression, therapeutic adaptation, and chemoresistance. This study investigated the relationship between TMZ responsiveness and the expression of selected lncRNAs in GBM cell lines exhibiting distinct sensitivity profiles. Methods: Human GBM cell lines (A172, U87, and T98G) and normal human astrocytes (NHA) were exposed to TMZ for 24–72 h. Cell viability, cell cycle distribution, MGMT protein expression, and expression levels of nine selected lncRNAs were analysed using MTT assay, flow cytometry, Western blot, and quantitative RT-PCR, respectively. Results: TMZ induced dose- and time-dependent reductions in cell viability in all analysed cell lines. A172 cells exhibited the greatest TMZ sensitivity, whereas T98G cells displayed the highest resistance. TMZ-sensitive GBM cells demonstrated pronounced G2/M cell cycle arrest, while T98G cells showed minimal cell cycle perturbation. MGMT protein expression was markedly elevated in T98G cells and decreased following exposure to higher TMZ concentrations. Distinct lncRNA expression profiles were identified among GBM cell lines. MALAT1 expression was consistently reduced, whereas NCK1-AS1 was strongly upregulated, particularly in T98G cells. TMZ exposure induced significant alterations in H19, PVT1, OIP5-AS1, and NCK1-AS1 expression, suggesting their potential involvement in adaptive resistance mechanisms. Conclusions: Collectively, these findings indicate that selected lncRNAs, particularly H19, MALAT1, NCK1-AS1, and PVT1, may contribute to TMZ resistance in GBM and could be promising biomarkers and therapeutic targets for precision oncology approaches. Full article

Background/Objectives: Psoriasis is a chronic, immune-mediated inflammatory skin disorder affecting millions of individuals worldwide. It remains a therapeutic challenge due to the limited skin penetration of many drugs, adverse systemic effects, and the need for long-term management. Transferosomal nanoformulations containing natural products were proposed as a potential therapeutic tool. Methods: Transferosomes containing 20-hydroxyecdysone and resveratrol were prepared using the thin-film hydration method followed by probe ultrasonication, generating several formulation variants differing in composition. The vesicles were characterized by dynamic light scattering (DLS) and nanoparticle tracking analysis (NTA) to determine size, polydispersity index (PDI), and zeta potential. Furthermore, time-domain nuclear magnetic resonance (TD-NMR) relaxation measurements were employed to evaluate local molecular dynamics and membrane fluidity, providing deeper insights into the structural integrity and elasticity of the transferosomal systems. The stability of the nanoformulations was assessed for one month in water and phosphate-buffered saline (PBS). Viability was evaluated in vitro using the MTS assay on human epidermal keratinocyte (HEK) and psoriasis-patient derived human epidermal keratinocyte (PHEK) cell lines, alongside antimicrobial profiling against four representative human skin microbiome strains. Acute toxicity was further examined in vivo using the Danio rerio FET test. Results: The formulations demonstrated high physicochemical stability over the tested period, maintained desirable particle sizes within 100–200 nm, and showed no cytotoxicity toward skin-associated bacteria or in the zebrafish model. Conclusions: The developed nanoformulations present suitable properties in terms of safety and stability and can be considered for potential use in psoriasis treatment. Full article