Search Results (13,656)

The effective and rapid separation of oil–water emulsions at room temperature, particularly under harsh environmental conditions like acid–base fluctuations, high salinity, and the coexistence of surfactants, remains a significant challenge in oily wastewater treatment. To address this, a novel amphiphilic demulsifier, MOF-74@SiO₂-GPTMS grafted ANP (MSG-ANP), was synthesized by first modifying MOF-74@SiO₂ (MS) with γ-glycidoxypropyltrimethoxysilane (GPTMS) to create epoxy-functionalized MSG particles, followed by grafting the non-ionic polyether C₁₂–C₁₄ aliphatic polyethylene oxide polyoxypropylene (ANP) onto MSG. Bottle tests demonstrated that MSG-ANP achieved a high demulsification efficiency of 93% within 15 min for oil-in-water emulsions at room temperature. It exhibited excellent environmental tolerance, maintaining efficiencies of 89% at pH 3.0, 82% at pH 11.0, and 95% under high salinity (50,000 mg/L, pH 6.8). Furthermore, MSG-ANP effectively treated surfactant-stabilized emulsions, exceeding 96% efficiency against both cetyltrimethylammonium bromide and sodium dodecyl sulfate after 30 min, outperforming commercial demulsifiers SP-169 and AR-331 by factors of 1.2 and 1.6, respectively. This superior performance stems from synergistic hydrogen bonding (via hydroxyl, ether, ester, Fe-O, and Si-O groups) destabilizing the interfacial film and electrostatic neutralization of coalescing charged droplets. Consequently, MSG-ANP presents a promising solution for rapid, room-temperature demulsification across a wide pH range and under high-salinity conditions. Full article

This study investigates the structural transformation from the γ-phase into the α-phase in bio-based nylon 5,6 fibers during in situ uniaxial stretching, using X-ray diffraction (XRD) and density functional theory (DFT) calculations. Initially, nylon 5,6 films exhibited a well-defined γ-phase crystalline structure, and the as-spun fibers also retained a γ-phase-dominant structure with partial coexistence of α-phase components. Due to the lattice similarity between the γ- and α-phases, phase separation was challenging in the direction perpendicular to the fiber axis (ab-plane). However, the analysis of the (004) diffraction peaks along the fiber axis (c-axis) enabled the quantitative evaluation of each crystalline component. As the stretching progressed, the α(004) peak intensity gradually increased, indicating a continuous γ-to-α structural transition. Furthermore, DFT calculations revealed that the α-phase has lower energy than the γ-phase, supporting the thermodynamic favorability of the phase transition during elongation. These results provide a comprehensive understanding of the crystalline structure and transformation mechanism in environmentally friendly nylon fibers from both experimental and theoretical perspectives, and offer foundational insights for developing nylon materials with desirable properties through the precise control of crystal phase structures. Full article

Nanoporous gold nanoparticles (np-AuNPs) combine inertness, a nanoscale structure, and a porous framework with high surface area, conductivity, and biocompatibility, making them ideal for biosensing, catalysis, fuel cells, and drug delivery. Their open pore structure and low-coordinated atoms enhance biomolecule capture and mass transfer, while their tunable size, pore volume, and ease of surface modification make them promising biosensor transducers. However, synthesizing colloidal np-AuNPs in a simple way with controllable size and scalability remains challenging. The existing approaches mostly rely on specialized equipment, complex setups, and expert knowledge, while still facing challenges in terms of scalability. In this study, we present a simple, seedless, wet-chemical synthesis of colloidal np-AuNPs via the co-reduction of Au/Ag alloys followed by dealloying. By adjusting the Au:Ag ratio, we produced np-AuNPs sized ~120–530 nm, which were immobilized on electrodes for detecting lipopolysaccharide (LPS), a toxic component of Gram-negative bacterial membranes. The LPS biosensor exhibited excellent sensitivity towards detecting wild-type LPS, with a low limit of detection (LOD) of 0.1244 ng/L. This work demonstrates the effective synthesis and application of np-AuNPs in LPS biosensing. Full article

Background/Objectives: Rice production faces threats from rising temperatures, demanding thermotolerant varieties. This study characterizes transcriptomic dynamics and identifies Hsp101-1 (heat shock protein 101-1)-associated gene regulatory modules in rice under reproductive-stage heat stress. Methods: Transcriptomics and WGCNA (weighted gene co-expression network analysis) were conducted in flag leaves and spikelets for wild-type (WT) and Hsp101-1-overexpressing (OE) lines under 40 °C stress at six time points (0–24 h) to reveal the change in gene expressions. Results: The number of DEGs (differentially expressed genes) revealed substantial pre-existing differences in WT and OE lines. Pre treatment, OE flag leaves showed 545 upregulated and 676 downregulated DEGs versus WT leaves. Post heat shock, the number of DEGs in flag leaves and spikelets was significantly reduced by 70–80%. KEGG enrichment of common DEGs across time points showed both WT and OE flag leaves enriched for ribosome biogenesis, ribosomes, and chaperones/folding catalysts. WGCNA identified that the MEdarkslateblue module correlated negatively with WT and positively with OE flag leaves. The MEturquoise module was suppressed at 1 h but activated by 8 h. Spikelet analysis identified the MElightpink4 module (negative correlation with WT, positive with OE) and a similarly dynamic MEturquoise module. Venn analysis identified 76 shared module genes, 71 of which were upregulated in the OE line, indicating that Hsp101-1 activates common protective targets. Hsp101-1’s expression in the WT line was low basally, significantly upregulated at 1–8 h post shock, and returned to low levels by 24 h. Conclusions: Hsp101-1 enhances thermotolerance by (1) constitutively pre-stabilizing transcriptomic networks and reducing transcriptional fluctuations under heat stress and (2) modularly coordinating tissue-specific responses, providing a climate resilience framework. Full article

Aspergillus fumigatus is an opportunistic filamentous fungus that primarily affects the respiratory tract of the human body. Depending on its host’s immune response, the pathogen can cause invasive pulmonary aspergillosis (IPA). Biofilm formation by A. fumigatus increases virulence and resistance against antifungals and immune response and is one important factor in IPA development. Here, two human-like models, precision cut lung slices (PCLS) and a biofilm co-culture model, have been developed to test the anti-biofilm activity of voriconazole, amphotericin B, as well as luliconazole against A. fumigatus. In both assays, metabolically active A. fumigatus biofilms were examined at different biofilm developmental stages using an XTT assay. A decrease in the metabolic activity of the fungal biofilms was detected for each of the tested agents in both assays. Significant anti-biofilm effects exist against early-stage biofilm in the co-culture model. In the PCLS assay, amphotericin B showed the strongest inhibition after 24 h. In conclusion, the applied PCLS ex vivo model can be used to study the property and activity of certain antifungal compounds against Aspergillus biofilm. With its close resemblance to human conditions, the PCLS model has the potential for improving the current understanding of biofilm treatments in laboratory settings. Full article

This study investigates the optimal duration for forming a uniform oxide layer and evaluates its influence on water-splitting performance. We selected a Ti₅₀Cu₃₂Ni₁₅Sn₃ amorphous ribbon, which is known to simultaneously form anatase TiO₂ and Sn oxide via a single hydrothermal process. Hydrothermal treatments were conducted at 220 °C in 150 mL of distilled water for durations of 3 and 6 h. The process successfully formed nanoscale metal oxides on the alloy surface, with the uniformity of the oxide layer increasing over time. The amorphous phase of the alloy was retained under all conditions. X-ray photoelectron spectroscopy (XPS) analysis confirmed the formation of TiO₂ and SnO_x, while Cu and Ni remained in their metallic state. Furthermore, we verified the coexistence of these oxides with metallic Ti and Sn. Photoelectrochemical analysis showed that the sample treated for 6 h exhibited the best water-splitting performance, which correlated directly with the most uniform oxide coverage. This time-controlled hydrothermal oxidation method, using only water, presents a promising and efficient approach for developing functional surfaces for electronic and photoelectrochemical applications of metallic glasses (MGs). Full article

Peanut cultivation currently plays a minor role in Portuguese agriculture, despite the country’s favorable soil and climatic conditions. In the Azores archipelago, where agriculture is a key economic activity, peanut production has recently sparked interest among rural producers. Weeds pose a major threat to crop development, particularly for short-cycle species like peanuts. This study aimed to determine the period prior to weed interference (PPI) in peanut crops under two row spacings (40 cm and 60 cm) on São Miguel Island, Azores. Eight treatments were established—0–15, 0–30, 0–45, 0–60, 0–75, 0–90 days after emergence (DAE), full-season coexistence, and a weed-free control—to represent increasing periods of weed competition. A randomized block design with four replicates was used for each spacing. The weed community included eight species, with Cyperus spp., Digitaria spp., Amaranthus blitum, and Portulaca oleracea being the most prevalent. Weed interference throughout the entire cycle led to yield losses exceeding 81% and 86% at 40 cm and 60 cm row spacings, respectively. The PPI was defined at a 5% yield reduction threshold, which is a commonly accepted benchmark in weed science to determine the beginning of the critical period of weed interference. Full article

TP53 genetic alterations represent a critical molecular feature in diffuse large B-cell lymphoma (DLBCL), with well-established associations with aggressive disease behavior and therapeutic resistance. However, significant controversy persists regarding the clinical utility of p53 immunohistochemical (IHC) expression as a surrogate marker. This study presents a thorough investigation of TP53 genetic alterations and their correlation with p53 protein expression in 664 cases of DLBCL. Using targeted next-generation sequencing (tNGS), we identified TP53 alterations (mutations and/or copy number losses (CNLs)) in 170 cases (25.6%). Among them, 161 cases had mutations. Concurrent analysis of copy number variations (CNVs) in 109 cases revealed TP53 CNLs in 17.4% (19/109), with 68.4% (13/19) of these showing coexisting mutations. Immunohistochemical evaluation of p53 expression in 371 cases demonstrated strong positivity (≥65% cells) in 21% (78/371), complete negativity (<1%) in 5.7% (21/371), and wild-type pattern (1–65%) in 73.3% (272/371) of cases. The p53 IHC laboratory-developed test (LDT) showed 79.2% sensitivity and 91.6% specificity for detecting TP53 alterations overall, though sensitivity varied significantly by mutation type: 86.2% for missense mutations but only 14.3% for nonsense mutations. Clinically, cases with TP53 alterations exhibited more aggressive disease characteristics, including higher ECOG performance scores, increased frequency of B symptoms, and poorer initial treatment responses (complete response rate 68.3% vs. 82.5% in wild-type cases). Most importantly, TP53 genetic alterations, but not p53 protein expression patterns, emerged as an independent prognostic factor for progression-free survival. Our findings demonstrate that tNGS effectively identifies most TP53 alterations and complementary CNV analysis enhances detection of copy number losses. The p53 IHC LDT serves as a useful but imperfect screening tool, with high specificity but variable sensitivity depending on mutation types. These results have important implications for molecular diagnostics in DLBCL, supporting the necessity for comprehensive genetic testing rather than reliance on protein expression analysis alone for accurate risk stratification and treatment planning. Full article

Background/Objectives: Generalized anxiety disorder (GAD) is one of the most commonly diagnosed anxiety disorders in primary care. The global lifetime prevalence of GAD is estimated at 3.7%, ranging from 1.6% in low-income countries to 5.0% in high-income countries, underscoring its widespread impact. Given the frequent co-occurrence of GAD with obesity, this association has important clinical implications, particularly for screening, prevention, and treatment strategies. The aim of this review is to identify potential biological mechanisms linking obesity and GAD, summarize the current state of knowledge in this area, and highlight existing research gaps, as well as directions for future research. Methods: This narrative review is based on the literature published between 2015 and 2025 concerning the co-occurrence of GAD and obesity, with a focus on potential shared mechanisms including HPA axis dysregulation, chronic inflammation, oxidative stress, insulin resistance, gut–brain axis and microbiota dysbiosis, sleep disturbance, and maladaptive eating behaviors. Results/Conclusions: A growing body of evidence suggests an important, albeit still ambiguously defined, relationship between obesity and GAD. GAD and obesity may reinforce each other, leading to a mutually reinforcing relationship. Despite growing interest, high-quality prospective and interventional studies focusing specifically on GAD are lacking. A potentially effective therapeutic approach should be integrated and multidisciplinary, combining psychological, pharmacological, and lifestyle interventions. It may also be beneficial for clinicians to consider routine assessment of anxiety in patients with obesity and, conversely, to monitor metabolic risk in individuals with GAD. Such an approach, targeting both mental and metabolic domains, holds promise for improving outcomes. Full article

Background: One in seven youth experiences a mental disorder, accounting for 13% of the global disease burden. The family environment is a modifiable factor for the prevention of mental disorders. While evidence-based online parenting programs exist, engagement by immigrant families, such as Indian-origin families in Australia, remains low. Objective: To explore perceived barriers of Indian-origin parents and co-create strategies to build cross-cultural bridging interventions to increase their engagement in parenting programs. Method: A qualitative co-design method was used, and participants were selected using a set of inclusion criteria through a criterion-based sampling approach. Eight videoconference workshops were conducted with 23 Indian-origin parents living across Australia, incorporating scenarios, roleplay, and vignettes. Data were analysed using Braun and Clarke’s inductive coding approach. Results: One central theme and six design principles were developed. The central theme, low engagement with parenting programs, encompassed five factors that contribute to low engagement: ‘parenting programs’ is not a concept in India; limited awareness of parenting programs available in Australia; lack of time to engage in parenting programs; misalignment between parenting program content and real-world parenting challenges; and an ‘I know how to parent’ mindset. The six design principles were: acknowledge culture shock and acculturation; use a collaborative approach; include content specific to immigrant parents and children; adopt cross-cultural perspectives; use short and interactive bilingual pedagogic tools; and use focused dissemination and marketing. Conclusions: This study’s findings formed the foundation for developing a cross-cultural bridging intervention to connect Indian-origin parents with existing online parenting programs. Full article

This narrative review consolidates existing evidence about the interaction between Epstein-Barr virus (EBV) and SARS-CoV-2 in cancer development. EBV is a recognized oncogenic driver, whereas COVID-19 may heighten cancer risk by immunological dysregulation, persistent inflammation, and reactivation of latent viruses. We underscore molecular similarities (e.g., NF-κB activation, T-cell exhaustion) and clinical ramifications for high-risk individuals, stressing the necessity for interdisciplinary research to alleviate dual viral risks. EBV, a well-known oncogenic virus, has been linked to numerous malignancies, including lymphomas, nasopharyngeal carcinoma, and gastric cancer. Through the production of viral proteins that interfere with immune evasion, cellular signaling, and genomic integrity, it encourages malignant transformation and ultimately results in unchecked cell proliferation. Because of its capacity to induce tissue damage, immunological dysregulation, and chronic inflammation, COVID-19, which is brought on by the SARS-CoV-2 virus, has become a possible carcinogen. The virus’s influence on cellular pathways and its long-term effects on the immune system may raise the chance of malignancy, particularly in people with pre-existing vulnerabilities, even if direct correlations to cancer are still being investigated. When two viruses co-infect a host, the review highlights the possibility of synergistic effects that could hasten the development of cancer. It describes how overlapping mechanisms like inflammation, immune suppression, and viral reactivation may be used by a combined EBV and COVID-19 infection to exacerbate carcinogenic processes. Gaining an understanding of these relationships is essential for creating tailored treatment plans and enhancing cancer prevention in high-risk groups. Full article

Monkeypox virus (MPXV) experienced an unprecedented global outbreak in 2022, characterized by a significant departure from historical patterns: a rapid spread of the epidemic to more than 110 non-traditional endemic countries, with more than 90,000 confirmed cases; a fundamental shift in the mode of transmission, with human-to-human transmission (especially among men who have sex with men (MSM)) becoming the dominant route (95.2%); and genetic sequencing revealing a key adaptive mutation in a novel evolutionary branch (Clade IIb) that triggered the outbreak. These features highlight the significant evolution of MPXV in terms of host adaptation, transmission efficiency, and immune escape ability. The aim of this paper is to provide insights into the viral adaptive evolutionary mechanisms driving this global outbreak, with a particular focus on the role of immune escape (e.g., novel mechanisms of M2 proteins targeting the T cell co-stimulatory pathway) in enhancing viral transmission and pathogenicity. At the same time, we systematically evaluate the cross-protective efficacy and limitations of existing vaccines (ACAM2000, JYNNEOS, and LC16), as well as recent advances in novel vaccine platforms, especially mRNA vaccines, in inducing superior immune responses. The study further reveals the constraints to outbreak control posed by grossly unequal global vaccine distribution (e.g., less than 10% coverage in high-burden regions such as Africa) and explores the urgency of optimizing stratified vaccination strategies and facilitating technology transfer to promote equitable access. The core of this paper is to elucidate the dynamic game between viral evolution and prevention and control strategies (especially vaccines). The key to addressing the long-term epidemiological challenges of MPXV in the future lies in continuously strengthening global surveillance of viral evolution (early warning of highly transmissible/pathogenic variants), accelerating the development of next-generation vaccines based on new mechanisms and platforms (e.g., multivalent mRNAs), and resolving the vaccine accessibility gap through global collaboration to build an integrated defense system of “Surveillance, Research and Development, and Equitable Vaccination,” through global collaboration to address the vaccine accessibility gap. Full article

Under the background of uncertainty brought by the rapid development of AI, participation in AI standardisation is becoming the key for strategic emerging enterprises (SEEs) to break through and achieve sustainable development. This paper selects listed SEEs from the China Strategic Emerging Industries Composite Index jointly issued by China Securities Index Co., Ltd. and the Shanghai Stock Exchange in 2017 as the initial sample. We collect 3430 observations from 380 companies spanning 2010 to 2023. This paper employs a two-way fixed effects model incorporating enterprise clustering. It thoroughly investigates and empirically tests how participation in AI standardisation affects the sustainable development of SEEs under uncertainty. It is found that participation in AI standardisation in the context of uncertainty has a significant positive effect on the sustainable development of SEEs, and this conclusion still holds after employing instrumental variables, difference-in-difference, and a series of robustness tests. Mechanism tests indicate that two transmission paths exist between participation in AI standardisation and the sustainable development of SEEs under uncertainty: digital technology innovation and the dynamic capabilities in the dimensions of learning and absorption as well as change and reconfiguration. However, the dynamic capabilities in the coordination and integration dimensions do not play a significant mediating role. Heterogeneity analyses indicate that participation in AI standardisation contributes more significantly to the sustainable development of SEEs that are not state-owned, face lower environmental and information uncertainty, and are under higher economic policy uncertainty. The findings enrich the research related to AI standardisation and firm sustainability and provide policy recommendations for the sustainable development of SEEs in the context of uncertainty. Full article

Background/Objectives: RAS mutations are among the most common genetic alterations in thyroid cancer and are generally associated with less aggressive behavior. However, when co-occurring with TERT (telomerase reverse transcriptase) promoter mutations, known markers of poor prognosis, tumors exhibit markedly more aggressive features. The allele frequency (AF) of RAS may serve as a potential indicator of clonal dominance and the likelihood of additional high-risk mutations, such as TERT mutation. This study aims to assess whether a high RAS AF correlates with the presence of coexisting TERT promoter mutations and other molecular alterations. Methods: A retrospective chart review was performed on 111 patients with thyroid nodules harboring RAS mutations, either alone or in combination with TERT promoter mutations. All patients underwent molecular testing with ThyroSeq v3 and subsequent thyroidectomy at McGill University teaching hospitals. RAS AF was analyzed in relation to TERT mutation status, nodule size, and other molecular alterations including copy number alterations (CNA) and gene expression profiles (GEP). Results: The mean RAS AF was significantly higher in nodules with both RAS and TERT mutations (38.1%) compared to those with RAS mutations alone (22.1%) (p = 0.002). Nodules with coexisting TERT mutations were also significantly larger (mean size: 3.7 cm vs. 2.4 cm; p = 0.005). Malignant nodules, regardless of TERT status, showed a trend toward higher RAS AF than benign nodules (23.0% vs. 16.3%; p = 0.052). Higher RAS AF was also associated with the presence of CNA and/or GEP positivity. Notably, GEP was positive in 100% of nodules with both RAS and TERT mutations, compared to 37.5% in RAS-only nodules (p = 0.002). Conclusions: A high RAS AF increases the likelihood of a TERT promoter mutation and other genetic alterations, highlighting the importance of RAS AF in optimizing patient care and management. Full article

Polystyrene microplastic (MP) and its co-existing contaminants may exert different toxic effects on its surrounding aquatic organisms. In order to detect the intestinal harmful responses, tilapia were subjected to exposure with 75 nm of MPs, 100 ng·L⁻¹ of sulfamethoxazole (SMZ), 5 ng·L⁻¹ of BDE153, and combinations thereof over periods of 2, 4, and 8 days. Enzymatic assays, transcriptomics, proteomics, and metabolomics were employed to evaluate intestinal histopathological effects. Results showed that significant reductions were observed in ATP, ROS, SOD, EROD, lipid metabolism-related enzymes, pro-inflammatory cytokines (TNFα and IL-1β), and apoptosis marker caspase 3 across all groups at day 8. Histological evaluation revealed diminished goblet cell density, with distinct vacuole formation in the BDE153+MPs group. KEGG pathway analysis highlighted disruptions in endocytosis, MAPK signaling, phagosome formation, and actin cytoskeleton regulation. Proteomic findings indicated notable enrichment in endocytosis (decreased sorting nexin-2; increased Si:dkey-13a21.4), MAPK/PPAR signaling, protein processing in the endoplasmic reticulum (Sec61 subunit gamma), and cytoskeletal modulation (reduced fibronectin; elevated activation peptide fragment 1), with or without SMZ and BDE153. Metabolomic profiling showed significant alterations in ABC transporters, aminoacyl-tRNA biosynthesis, protein digestion and absorption, and linoleic acid metabolism. In summary, these findings suggest that BDE153 and MPs synergistically exacerbate intestinal damage and gene/protein expression over time, while SMZ appears to exert an antagonistic, mitigating effect. Full article