Search Results (11,084)

Cellulose is a complex polysaccharide that serves as the primary structural component of plant cell walls. It is highly suitable for packaging films due to its inherent and tunable properties, which offer a sustainable alternative to conventional plastics. In this study, cellulose was extracted from vegetable waste (kale and cabbage) and processed into films using LiCl/N,N-dimethylacetamide (DMAc) as the solvent system. The regenerated cellulose films were characterized and compared with a film prepared from commercial microcrystalline cellulose (MCC) using the same procedure. The vegetable-waste films showed a lower degree of crystallinity than the MCC film. SEM micrographs revealed that the vegetable-waste films possessed smooth and uniform surfaces. Furthermore, they demonstrated good transparency, ductility, and thermal stability. Biodegradation tests indicated rapid decomposition of the vegetable-waste films, which fully degraded within 10 weeks, whereas the MCC film required 16 weeks. The cabbage-derived film exhibited a smoother surface and slightly better mechanical properties than the kale-derived film, suggesting that differences in the cellulose source can influence the regeneration process and, consequently, the properties of the resulting films. Overall, this work demonstrates that vegetable waste can be effectively upcycled into eco-friendly, low-cost cellulose films with strong potential for use in various sustainable material applications. Nevertheless, for edible applications, cytotoxicity testing is required to confirm the absence of residual health-risk reagents such as LiCl and DMAc in the resulting films. Full article

Goose blood has anticancer properties and was recorded in ancient China, but the specific molecular mechanisms underlying this effect still require further exploration. In this study, SW1990 cells were treated with goose serum or plasma, and transcriptome analysis was performed to explore the function of goose blood on cancer cells. Metabolomic profiling was also performed on goose serum, goose plasma, chicken serum, and chicken plasma to identify the bioactive substances responsible for the anticancer effect. The study examined the effects of goose plasma and serum on SW1990 cells and compared the metabolites between goose and chicken blood. Wound scratch, CCK-8, and Annexin V-PI assays showed that goose plasma and serum inhibited SW1990 cell proliferation at 24 and 48 h. Both treatments reduced cell viability, with serum inducing early and late apoptosis and plasma inducing late apoptosis. RNA sequencing (RNA-seq) identified 2259 (1418 upregulated, 841 downregulated) and 2731 (1844 upregulated, 887 downregulated) differentially expressed genes (DEGs) in the plasma and serum groups versus the negative control (NC), respectively, and 689 DEGs between the plasma and serum groups. Gene Ontology (GO) and KEGG pathway analyses revealed that the DEGs were enriched in processes such as lipid metabolism, JAK-STAT, and IL-17 pathways. Untargeted liquid chromatography–tandem mass spectrometry (LC-MS/MS) analysis identified distinct metabolites in goose and chicken blood, with unique metabolites and differential ones between groups. In SW1990 cells, four metabolite subclusters matched the plasma and serum effects. In summary, goose blood can suppress cancer cells by regulating gene expression to affect the key signaling pathways involved in cancer cell apoptosis and autophagy. Certain metabolites present at high concentrations in goose blood, such as cucurbitacin D and Oleoyl-L-carnitine, may also contribute to the inhibition of cancer cell proliferation and migration. These findings suggest that goose blood holds broad application prospects as a future auxiliary drug for cancer treatment, and this study provides a theoretical basis for the further application of goose products. Full article

Chronic inflammatory skin diseases, including psoriasis, hidradenitis suppurativa (HS), and atopic dermatitis (AD), are increasingly recognized as systemic disorders associated with chronic immune dysregulation. Growing evidence supports their links with metabolic disorders, reflected in heightened interest in therapeutic strategies targeting the immunometabolic axis. This review summarizes current knowledge on the role of glucagon-like peptide-1 receptor agonists (GLP-1RAs) in the regulation of immune and metabolic processes in chronic inflammatory skin diseases, with particular emphasis on molecular mechanisms and available experimental and clinical data. GLP-1RAs, widely used in the treatment of type 2 diabetes and obesity, may also exhibit anti-inflammatory and immunomodulatory properties beyond their classical metabolic effects. GLP-1 signalling can influence keratinocyte function, immune cell activity, and wound healing. Furthermore, it modulates multiple intracellular signalling pathways, including cAMP/PKA, AMPK, PI3K/Akt, and NF-κB, as well as immune axes such as IL-23/Th17/IL-17 and inflammasome-related signalling. Available evidence suggests that GLP-1RAs may reduce inflammation and disease activity in selected inflammatory dermatoses. However, current evidence remains limited and is based primarily on experimental studies, case reports, and small-scale observational studies. Further well-designed clinical trials are needed to better define the therapeutic potential of GLP-1RAs and their role in dermatological practice. Full article

Halide-based solid electrolytes have emerged as promising candidates for next-generation all-solid-state lithium metal batteries due to their high room-temperature ionic conductivity, wide electrochemical stability window, and favorable mechanical properties. This review provides a comprehensive overview of the fundamental structure–property relationships, Li⁺ transport mechanisms, and performance optimization strategies for Li₃MX₆-type halide solid electrolytes. The unique structural framework of halide electrolytes, characterized by close-packed anion sublattices (hexagonal close-packed and cubic close-packed) and edge-sharing [MX₆]³⁻ octahedral networks, establishes three-dimensional Li⁺ percolation pathways with low migration barriers (0.20–0.33 eV). This review concludes by identifying key challenges and future research directions, including high-entropy halide design, scalable aqueous synthesis methods, earth-abundant material alternatives, and integrated cell architectures that combine halide catholytes with complementary anolyte materials for practical all-solid-state battery applications. Full article

Bacterial membrane vesicles (BMVs), encompassing outer membrane vesicles (OMVs) released from Gram-negative bacteria and extracellular vesicles (EVs) released from Gram-positive bacteria, have emerged as promising vaccine platforms owing to their intrinsic immunostimulatory properties and capacity to deliver a wide range of antigens. Although conventional vaccines effectively prevent infectious diseases, their long-term efficacy is often limited by antigenic variation and reliance on a restricted number of licensed adjuvants. BMVs, as self-adjuvanting systems, enable both antigen delivery and innate immune activation. BMVs are nanoscale lipid bilayer structures enriched with pathogen-associated molecular patterns (PAMPs), facilitating their recognition and uptake by antigen-presenting cells. This leads to the activation of pattern recognition receptors and the induction of pro-inflammatory cytokines, type I interferons, and adaptive immune responses, including antibody production and Th1- and Th17-biased cellular immunity. Recent studies highlight the versatility of BMVs as vaccine platforms across bacterial, fungal, and viral infection models. BMVs induce protective immunity by promoting both systemic and mucosal immune responses, thereby reducing bacterial burden and limiting pathogen colonization across diverse infection models. These properties have supported their application in viral vaccine development, including influenza and SARS-CoV-2, with the potential to enhance mucosal immunity. Despite these advantages, challenges remain in standardization, safety, and antigen-loading efficiency. Engineered BMVs incorporating protein or mRNA antigens may further enhance antigen presentation and CD8⁺ T cell responses. This review summarizes the biological features, immunological mechanisms, and future potential of BMVs in vaccine development. Full article

Hyaluronic acid (HA), a native non-sulfated glycosaminoglycan of the extracellular matrix, has emerged as a central biomaterial in tissue engineering due to its biocompatibility, hydration capacity, and receptor-mediated bioactivity. Beyond its structural role, HA actively regulates cellular behaviors through interactions with receptors such as CD44 and RHAMM, with outcomes highly dependent on molecular weight, degradation state, and matrix context. Recent advances in chemical modification and crosslinking strategies have enabled the development of HA-based hydrogels, nanofibers, and composite systems with tunable mechanics and degradation profiles, supporting applications in bone, cartilage, vascular, and skin regeneration, as well as in emerging platforms such as 3D bioprinting and nanomedicine. However, inconsistent biological responses and limited clinical translation remain key challenges. This review integrates current understanding of HA synthesis, physicochemical properties, degradation, and receptor-mediated signaling, and establishes a mechanistic framework linking molecular characteristics, matrix mechanics, and cell responses. Building on this framework, we outline design strategies for multifunctional HA composites, advanced biofabrication approaches, and receptor-targeted systems, providing a basis for the rational engineering of next-generation HA-based biomaterials with improved translational potential. Full article

Reduced graphene oxide (rGO) wrapped with poly(styrenesulfonate) (PSS) forms a stable hybrid material (rGO/PSS) capable of producing ultrathin films with promising barrier properties for Direct Methanol Fuel Cell (DMFC) applications. These films aim to mitigate methanol crossover, one of the major limitations of DMFC technology. In this work, we investigate the mechanisms underlying the methanol barrier effect of rGO/PSS, while maintaining water permeability. Classical Molecular Dynamics simulations were employed to explore the structural and dynamic properties of rGO/PSS at different polymer ionization fractions in a solvent mixture of water, methanol, and hydronium. The influence of the sulfonation fraction on film self-assembly was analyzed, including its impact on PSS conformation, rGO sheet distribution, and PSS–rGO interactions. Finally, the effect of the rGO/PSS structure on solvent diffusion was investigated, and the mechanisms responsible for the selective transport of methanol were elucidated. Full article

Unlike newborns, tendon injuries in adults usually lead to fibrotic scarring rather than functional regeneration. This difference is primarily due to the loss of neonatal extracellular matrix (nECM) signaling in adulthood. In this study, we investigated the molecular mechanisms by which a key neonatal ECM proteoglycan, biglycan (Bgn), orchestrates the behavior of tendon stem/progenitor cells (TSPCs) within a scaffold-free 3D cell sheet microenvironment that recapitulates native tendon architecture. Through immunofluorescence screening, we confirmed that Bgn is the predominant proteoglycan in neonatal rat Achilles tendons. Functional validation showed that adding Bgn to cell sheet cultures promoted TSPCs proliferation, maintained stem cell properties, induced tendon differentiation, and encouraged anisotropic alignment—effects similar to those of intact neonatal ECM. Immunodepletion experiments confirmed the causal role of Bgn. Notably, transplanting Bgn-conditioned TSPCs sheets into a rat full-thickness Achilles tendon defect model significantly restored final tensile load, collagen maturation, and gait function. These outcomes were statistically indistinguishable from those of the uninjured contralateral limb. These findings confirm that Bgn-functionalized cell sheet therapy is a viable translational strategy that can effectively recreate a natural 3D regenerative microenvironment. This work sheds light on the mechanisms involved in the determination of stem cell fate by the ECM and establishes Bgn-functionalized cell sheet therapy as a translatable, scaffold-free strategy for overcoming fibrotic repair and restoring functional tendon architecture. Full article

Cardiovascular diseases remain the leading cause of mortality in developed countries. Among these conditions, acute myocardial infarction (AMI) is associated with particularly high rates of cardiac morbidity and mortality. Cardiac development in mammals is primarily dependent on cardiomyocyte (CM) proliferation during embryonic and early postnatal stages. However, following birth, the proliferative capacity of CMs declines markedly, with only limited cellular renewal occurring during adult life in response to pathological injury. Consequently, the irreversible loss of functional cardiomyocytes and the subsequent formation of fibrotic scar tissue frequently lead to persistent cardiac dysfunction and progressive impairment of cardiac physiology. Cardiomyocyte self-renewal is a tightly regulated process involving multiple molecular pathways. Among factors implicated in this regulation, microRNAs (miRNAs) have emerged as key modulators coordinating both cardiac development and tissue repair mechanisms. In this context, extracellular vesicles (EVs) have attracted considerable interest as potential modulators of these regenerative processes. In particular, mesenchymal stromal cells (MSCs) represent a promising therapeutic platform due to their immunomodulatory and anti-fibrotic properties demonstrated across multiple in vitro and in vivo models. Furthermore, the therapeutic potential of MSC-derived EVs can be enhanced through bioengineering approaches aimed at improving targeted molecular delivery. In this review, we summarize recent advances in the development and application of EV-based therapeutic strategies, with particular emphasis on their potential use as advanced therapy medicinal products (ATMPs) for cardiovascular regeneration and repair. Full article

Opportunities abound in microfluidic technologies to impact how we understand extremely complex systems with many constituents which change with time and space. In these technologies, separation science plays a central role towards understanding everything from biology and healthcare to environmental monitoring to the search for life in the Solar system. Separations can amplify the capabilities of detection modalities by isolating targets and/or increasing their concentration while removing background constituents which can interfere with their sensing. In essence, separations increase the amount of information that can be gathered from a sample. The ideal features of next-generation separations capability are present in gradient insulator-based dielectrophoresis (g-iDEP), enabled by the length scale and precision of microfluidics. It acts through electric field interactions with particles, which enables unbiased (label-free) separations since all relevant particles, from atoms to cells, have an accessible response to electricity—either through linear (electrophoresis) or higher-order gradient (dielectrophoresis and related) effects. The technique isolates and concentrates, enabling improved detection function and multidimensional separations. Its foundational theoretical capabilities give it separations power on the order of 1:10⁸, beyond the resolving power of the best mass spectrometers and ultra-high resolution spectroscopies. Experimental evidence is amassing that shows it to be a powerful tool that can resolve tiny differences in cells (antibiotic resistance versus susceptible in unlabeled paired isolates across many species) and differentiate single-point mutations in proteins. Its capabilities are still emerging, and this work aims to quantify the current practice and connect those approaches to the ultimate capabilities of the technique towards quantifying the dynamic range and resolving power of the strategy as a whole. The technique uses two methods of quantifying the electrophysical properties of the target, voltage sweep and spatial methods. The voltage sweep method is lower-resolution and serves as a search mode, while the spatial method is higher-resolution and quantifies the properties over a smaller defined range determined via the sweep method. These quantification methods are examined by collating existing experimental data, performing relevant Monte Carlo simulations, and finite element model calculations. These are summarized to understand the mechanisms currently limiting the technique, facilitate quantitative comparisons with traditional separation science capabilities in terms of resolution and dynamic range, and compare them to the theoretical limits of the strategy. Full article

Background/Objectives: Merkel cell polyomavirus (MCPyV) is a ubiquitous virus strictly associated with Merkel cell carcinoma (MCC), a rare and aggressive skin cancer. MCPyV oncogenic properties are associated mainly with early protein expression, integration, and LT truncation. MCPyV can also interact with DNA Damage Response (DDR) mechanisms, contributing to oncogenesis and tumor progression. In this work, we investigated the correlation between MCPyV and MCC and evaluated the mRNA expression profiles of DDR genes in virus-positive and -negative tumors. Methods: A total of 19 formalin-fixed paraffin-embedded biopsies were acquired from patients diagnosed with MCC. After DNA and RNA extraction, the DNA was used for MCPyV detection via qPCR and for sequencing analysis of the early, late, and non-coding control viral regions and the extracted RNA was used for MCPyV transcripts, miRNA detection and for the evaluation of several DDR genes expression such as ATM, ATR, CHK1, CHK2, H2AX, Rad51, p53, and p21, in MCPyV-positive and -negative samples via reverse transcription, PCR, and qPCR. Results: MCPyV presence was detected in 11/19 samples, all characterized by viral integration, LT truncation, and early region expression only. Furthermore, higher mRNA levels of DDR genes were observed in MCPyV-positive tumors compared with the negative ones. Conclusions: Our findings support the role of MCPyV in MCC formation and suggest its involvement in the transcriptional regulation of DDR genes, which may influence tumor progression. Understanding the molecular interplay between MCPyV and the DDR may guide future research into plausible novel diagnostic and therapeutic strategies for virus-induced tumors. Full article

The food-packaging sector is undergoing a major transition driven by the environmental burden associated with petroleum-based plastics and the increasing demand for sustainable alternatives. In this context, biodegradable packaging materials capable of extending food shelf life through active preservation functions have attracted considerable interest. Cellulose is the most abundant natural polymer and an attractive candidate for sustainable packaging; however, it lacks intrinsic antimicrobial activity. In the present study, innovative carboxymethyl cellulose (CMC)-based composite films were developed by incorporating zinc oxide (ZnO) nanoparticles (NPs) and thyme essential oil (TEO) as antibacterial active agents. The obtained films exhibited strong antibacterial activity against both Escherichia coli and Staphylococcus aureus, completely eliminating planktonic cell viability after 3 h of contact and producing inhibition zones of up to 30 mm. In addition to their biological performance, the composite films showed improved mechanical and functional properties. ZnO NPs appear to act as multifunctional junctions within the CMC matrix, while the dispersed TEO droplets contribute, together with the inorganic phase, to reduced water-vapor transfer. The films retained good transparency in the visible range while exhibiting UV-A transmittance below 7%, indicating enhanced light-barrier performance. Preliminary tests on soft cheese indicated shelf-life extension up to 14 days at 4 °C, while in inoculated cheese slices packed in the composite films, S. aureus was not detected from the 3rd day. Overall, these results demonstrate the potential of CMC/ZnO/TEO composite films as biodegradable active packaging materials for perishable food products. Full article

Green seeds of Coffea arabica represent a rich source of bioactive compounds. This study aimed to compare the butanol-soluble (CA-BU) and the ethyl acetate-soluble (CA-EtAc) fractions in terms of their phytochemical composition and biological activity. As a first step, the fractions were analyzed by Fourier-transform infrared spectroscopy (FT-IR) and high-performance liquid chromatography coupled with mass spectrometry (HPLC–MS) in order to investigate the major constituents. Subsequently, CA-BU and CA-EtAc were evaluated for antioxidant effect, antimicrobial activity, antiproliferative properties, effects on the mitochondrial function, and on the chorioallantoic membrane. The CA-EtAc fraction was enriched in chlorogenic acids and catechins and showed superior antioxidant activity, whereas CA-BU displayed a broader profile of semi-polar polyphenols, conferring moderate antimicrobial effects and stronger antiproliferative activity in MCF-7 human breast adenocarcinoma cells, although with limited selectivity compared with HaCaT non-tumorigenic cells. Respirometric analysis demonstrated that CA-BU selectively inhibited mitochondrial oxidative phosphorylation Complex I (OXPHOS CI), without affecting Complex II (CII) or basal respiration, indicating a specific mitochondria-targeted mechanism. Both fractions were non-irritant and well tolerated in the chorioallantoic membrane (CAM) assay; CA-BU reduced vascular density. These findings demonstrate a clear mechanistic differentiation between the fractions, highlighting the decisive role of solvent polarity in obtaining extracts with distinct and targeted biological effects. Full article

Skin wound healing is a complex and highly coordinated biological process involving inflammation, cell migration and proliferation, angiogenesis, extracellular matrix remodeling and tissue regeneration. While the zebrafish-derived antimicrobial peptide AP10W exhibits broad-spectrum antimicrobial properties, its potential in tissue repair remains unexplored. Herein, we demonstrate that AP10W possesses intrinsic wound-healing capabilities, providing a preliminary investigation into its underlying mechanisms. In this study, using a full-thickness murine wound model and in vitro cell-based assays to evaluate the effects of AP10W on fibroblasts, keratinocytes, endothelial cells, and macrophages, we found that AP10W significantly promoted fibroblast and keratinocyte migration and proliferation. Furthermore, it enhanced endothelial cell motility, survival, and tube formation, while upregulating key pro-angiogenic factors, including Vascular endothelial growth factor A (VEGFA), Platelet-derived growth factor (PDGF), and Fibroblast growth factor 2 (FGF2). Concurrently, AP10W drove macrophage reprogramming from a pro-inflammatory M1 phenotype toward a pro-healing M2 state, as evidenced by upregulated Arginase-1 (Arg-1) and Interleukin-10 (Il-10) expression, alongside attenuated Tumor necrosis factor-alpha (Tnf-α), Interleukin-1 beta (Il-1β), Interleukin-6 (Il-6), and Inducible nitric oxide synthase (iNOS) levels. In vivo, the topical application of AP10W accelerated wound closure, markedly improving re-epithelialization, collagen deposition, vascularization, tissue perfusion, and skin appendage regeneration. Preliminary mechanistic studies revealed that AP10W increased YAP expression and nuclear translocation; conversely, the pharmacological inhibition of YAP significantly abrogated these pro-healing effects. Collectively, our findings identify AP10W as a multifunctional peptide with potent wound-healing properties, positioning it as a promising candidate for wound therapy. Full article

Vanadium borate (V₃BO₆) has recently been synthesized and identified as a promising material for use in energy storage applications, particularly as a potential anode for lithium-ion batteries. However, despite previous studies highlighting its electrochemical performance, a comprehensive understanding of its intrinsic mechanical, thermal, and vibrational properties remains limited. The compound crystallizes in an orthorhombic phase with the Pnma (No. 62) space group. To explore its intrinsic physical characteristics, full geometry optimization of the unit cell and atomic positions was performed using density functional theory (DFT) within the CASTEP framework. The Perdew–Burke–Ernzerhof (PBE) functional under the generalized gradient approximation (GGA) was used to model exchange–correlation effects. A plane-wave cut-off of 408 eV and a 6 × 6 × 13 Monkhorst–Pack grid were employed to ensure numerical convergence. The optimized lattice constants (a = 9.9025 Å, b = 8.4751 Å and c = 4.5354 Å) are highly consistent with experimental data, which confirms the reliability of the computational approach adopted. The elastic behaviour was further investigated using the first-principles strain-energy method, yielding nine independent elastic constants consistent with orthorhombic symmetry. The calculated bulk and shear moduli, along with the anisotropy parameters, suggest that V₃BO₆ has a favourable balance of mechanical robustness and moderate ductility. A Vickers hardness of 10.95 GPa and a B/G ratio of approximately 1.93 corroborate these findings. Additional parameters, such as Poisson’s ratio, Debye temperature and average sound velocities, were derived to gain deeper insight into the material’s thermomechanical performance. These results provide a solid theoretical foundation for understanding the mechanical stability and potential anode suitability of V₃BO₆ in lithium-ion battery systems. Full article