Search Results (414)

Heated tobacco products (HTPs) are marketed as lower-risk alternatives to conventional cigarettes; however, their toxicological impacts remain insufficiently characterized. This study evaluated the effects of HTP emissions on gene expression and mitochondrial function in comparison with conventional cigarettes. Whole cigarette smoke condensates (WCSCs), comprising both gas and particulate phases, were prepared from three commercially available HTPs and from 3R4F reference cigarettes. Human lung epithelial BEAS-2B cells were exposed to WCSCs at 3 μg nicotine/mL for 24 h, followed by transcriptome profiling using RNA sequencing. Principal component analysis demonstrated that HTP-WCSCs induced weaker gene expression changes than 3R4F-WCSC, with only modest variation among HTPs. Gene set enrichment analysis revealed that both HTP- and 3R4F-WCSCs significantly downregulated oxidative phosphorylation (OXPHOS)–related pathways, indicating potential mitochondrial impairment. Functional assays confirmed that both exposures elevated mitochondrial reactive oxygen species (ROS), while mitochondrial morphology, ATP production, membrane potential, and cytosolic ROS were largely unaffected. Collectively, these results show that although HTP emissions elicit weaker transcriptomic perturbations than conventional cigarette emissions, both converge on mitochondrial targets by suppressing OXPHOS gene expression and increasing mitochondrial ROS. Mitochondrial dysfunction may therefore represent a common mechanism underlying tobacco product toxicity. Full article

The growing threat of airborne biological agents necessitates rapid, sensitive, and portable detection systems to mitigate risks to public health and national security. We present a comprehensive overview of biosensor technologies developed for airborne biothreat detection, with a focus on aptamer-based electrochemical sensors. These sensors offer key advantages in portability, chemical stability, and adaptability for multiplexed detection in field settings. The urgency for real-time surveillance tools capable of identifying viral, bacterial, and toxin-based agents is discussed, particularly in the context of biodefense. Aerosolized particle capture strategies are reviewed, focusing on microfluidics for micron-sized particles and condensation-based systems for submicron-sized particles, which are preferred for their small-volume operation and seamless integration with biosensors. Key biosensor components are described, including recognition elements—such as aptamers—and transduction mechanisms like electrochemical impedance spectroscopy. EIS is highlighted for its label-free, miniaturizable, and real-time readout capabilities, making it well-suited for portable biosensors. Advances in sensing strategies for both viral and bacterial targets are explored, featuring innovations in nanoporous membrane platforms, nanomaterials, and multiplexed assay formats. Recent developments demonstrate improved sensitivity through nanopore-based signal amplification and enhanced selectivity using engineered aptamer libraries. The review concludes by addressing current limitations, including environmental stability, system integration, and the need for validation with complex real-world samples. Future directions point toward the development of fully integrated, field-deployable biosensing platforms that combine effective aerosol capture with robust and selective biosensing technologies. Full article

Phosphine (PH₃) is an important functional material that plays a pivotal role in semiconductor fields. As semiconductor technology rapidly advances toward smaller sizes and higher performance, the requirements for the purity of phosphine in chip manufacturing are becoming increasingly stringent. To address this, this study has designed a purification process for ultra-high purity phosphine, capable of achieving a purity level of 6N (99.9999%) for phosphine products. The process was simulated and analyzed using Aspen Plus to investigate the influence of various factors on the purity of phosphine products. In this design, the sensitivity analysis function was used to determine the optimal number of theoretical stages, feed stage, and reflux ratios for each rectifying column in the process. It was also found that an increase in rectifying column pressure is detrimental to the removal of low-boiling-point substances such as N₂ and O₂ from phosphine. Furthermore, a double-effect distillation process was designed. After adopting the double-effect distillation process, the heat duty on all condensers and reboilers would decrease by 27%, but the purity of the phosphine product would decrease from 99.999943% to 99.999936%. Finally, a control scheme was designed for the distillation column used to extract phosphine products, and the control effect was dynamically simulated and tested using Aspen Plus Dynamics. The test results showed that disturbances caused by a decrease in feed were much more difficult to control than those caused by an increase in feed, and that low-boiling-point impurities had a much greater impact on the purity of phosphine products than high-boiling-point impurities. In addition, the results of steady-state simulation indicate that CO₂ in phosphine is difficult to remove through distillation processes. Adding adsorption processes or membrane separation processes after distillation to remove CO₂ from phosphine is a research direction for improving the purity of phosphine. Full article

Extracellular particles (EPs), an umbrella term encompassing membrane-enclosed extracellular vesicles (EVs) and non-vesicular extracellular particles ([NVEPs], previously described as extracellular condensates [ECs]) contain a complex cargo of biomolecules, including DNA, RNA, proteins, and lipids, reflecting the physiological state of their cell of origin. Identifying proteins associated with EPs that regulate host responses to physiological and pathophysiological processes is of critical importance. Here, we report the findings of our study to gain insight into the proteins associated with NVEPs. We used samples from human semen, the rat brain, and the rhesus macaque (RM) brain and blood to assess the physical properties and proteome profiles of NVEPs from these specimens. The results show significant differences in the zeta potential, concentration, and size of NVEPs across different species. We identified 938, 51, and 509 total proteins from NVEPs isolated from rat brain tissues, RM blood, and human seminal plasma, respectively. The species-specific protein networks show distinct biological themes, while the species-conserved protein interactome was identified with six proteins (ALB, CST3, FIBA/FGA, GSTP1, PLMN/PLG, PPIA) associated with NVEPs in all samples. The six NVEP-associated proteins are prone to aggregation and formation of wide, insoluble, unbranched filaments with a cross-beta sheet quaternary structure, such as amyloid fibrils. Protein-to-function analysis indicates that the six identified proteins are linked to the release of dopamine, immune-mediated inflammatory disease, replication of RNA viruses, HIV-HCV co-infection, and inflammation. These interesting findings have created an opportunity to evaluate NVEPs for their potential use as biomarkers of health and disease. Additional in-depth studies are needed to clarify when and how these proteins sustain their physiological role or transition to pathogenic roles. Full article

The localization and remodeling of mRNPs is inextricably linked to translational control. In recent years there has been great progress in the field of mRNA translational control due to the characterization of the proteins and small RNAs that compose mRNPs. But our initial assumptions about the physical nature and participation of germ cell granules/condensates in mRNA regulation may have been misguided. These “granules” were found to be non-membrane-bound liquid–liquid phase-separated (LLPS) condensates that form around proteins with intrinsically disordered regions (IDRs) and RNA. Their macrostructures are dynamic as germ cells differentiate into gametes and subsequently join to form embryos. In addition, they segregate translation-repressing RNA-binding proteins (RBPs), selected eIF4 initiation factors, Vasa/GLH-1 and other helicases, several Argonautes and their associated small RNAs, and frequently components of P bodies and stress granules (SGs). Condensate movement, separation, fusion, and dissolution were long conjectured to mediate the translational control of mRNAs residing in contained mRNPs. New high-resolution microscopy and tagging techniques identified order in their organization, showing the segregation of similar mRNAs and the stratification of proteins into distinct mRNPs. Functional transitions from repression to activation seem to corelate with the overt granule dynamics. Yet increasing evidence suggests that the resident mRNPs, and not the macroscopic condensates, exert the bulk of the regulation. Full article

Background/Objectives: Polybia-MP1 (MP1) exhibits antimicrobial and anticancer properties. To improve selectivity toward acidic tumor microenvironments, we designed HMP1, a histidine-substituted analog of MP1, aiming to introduce pH-responsive behavior within physiological and pathological pH ranges. Methods: HMP1 was synthesized by replacing all lysine residues in MP1 with histidines. We characterized its surfactant properties and interactions with lipid monolayers composed of DPPC under varying pH and ionic strength conditions. Langmuir monolayer experiments were used to evaluate peptide-induced morphological changes and lipid packing effects at physiologically relevant lateral pressures. Results: HMP1 displayed pH-dependent activity between pH 5.5 and 7.5, inducing significant morphological reorganization of lipid domains without reducing the condensed phase area. Ionic strength modulated these effects, with distinct behaviors observed at low and physiological saline conditions. HMP1 preferentially interacted with cholesterol-enriched membranes, while MP1 did not induce comparable effects under the same conditions, as previously reported, at physiological lateral pressures. HMP1 also exhibited non-hemolytic properties and lower cytotoxicity compared to MP1. Conclusions: The lysine-to-histidine substitution conferred pH sensitivity to HMP1, enabling selective modulation of membrane organization based on lipid composition, packing, pH, and ionic environment. These findings highlight HMP1’s potential in targeted therapeutics and pH-responsive drug delivery systems. Full article

Transcription is a core hallmark of cancer, wherein many different proteins assemble at specific sites in the nucleus and act in concert to transcribe functionally relevant genes. Central to this process are transcription factors that bind to their cognate DNA motifs on enhancers and super-enhancers to recruit cofactors, coactivators, and epigenetic modifiers, thereby inducing or repressing gene expression. Super-enhancers drive oncogenic transcription, to which cancer cells become highly addicted and confer tumor dependencies on super-enhancer-driven transcription machinery. Transcriptional condensates (TCs) are nuclear membrane-less assemblies of DNA-binding transcription factors, transcription co-activators, and the transcriptional machinery (such as RNA polymerases, non-coding RNAs) formed through liquid–liquid phase separation (LLPS). The function of transcriptionally active oncogenic proteins and their interplay with nucleic acids are carried out within these biomolecular condensates, allowing them to spatiotemporally regulate oncogene expression and lead to the induction and maintenance of cancer. With this growing understanding, specific inhibitors and strategies targeting TC assembly and activation should be considered promising therapeutic opportunities for treating various tumors, including hematological malignancies. Full article

Vacuum membrane distillation (VMD) is a promising desalination technology, which is likely to be integrated with solar energy, and offers a sustainable solution to freshwater scarcity. However, its industrial application remains limited due to high specific energy consumption and water production costs. The key to improving VMD performance lies in enhancing the recovery of the latent heat of condensation. In this investigation, four different configurations are proposed; each differs in the method of condensation and energy recovery. The first is applied by using a basic condenser, preheating seawater with latent heat from vapor. The second is implemented by incorporating a liquid ring vacuum pump (LRVP), enabling both condensation and vacuum generation. The third is performed by coupling VMD with a heat pump, which operates by using a refrigerant fluid. Lastly, the fourth is employed by using mechanical vapor compression (MVC), where the vapor is compressed to recover heat efficiently. The results show that the VMD-MVC is the most efficient configuration, offering the lowest specific energy consumption (154.6 kWh/m³), the highest energy recovery rate (54.64%), the highest gained output ratio (GOR) of 5.52, and the lowest water production cost (4.6 USD/m³). In contrast, the VMD system coupled with a heat pump presented the highest water production cost (36.4 USD/m³) among all the evaluated configurations. Full article

Cellular organization relies on both membrane-bound organelles and membraneless biomolecular condensates formed through liquid–liquid phase separation. Recent discoveries reveal intricate coupling between lipid membrane organization and condensate assembly, reshaping our understanding of cellular compartmentalization. This review synthesizes multidisciplinary research using advanced techniques including super-resolution microscopy, fluorescence recovery after photobleaching, and in vitro reconstitution to examine lipid-condensate interactions. Lipid membranes serve as nucleation platforms that reduce critical concentrations for condensate formation by orders of magnitude through membrane anchoring and thermodynamic coupling, creating specialized microenvironments that substantially enhance enzymatic activities. Key regulatory mechanisms include phosphorylation-driven assembly and disassembly, membrane composition effects from cholesterol content and fatty acid saturation, and environmental factors such as calcium and pH. These interactions drive signal transduction through receptor clustering, membrane trafficking via organized domains, and stress responses through protective condensate formation. Dysregulation of lipid-condensate coupling, including aberrant phase transitions and membrane dysfunction, underlies metabolic disorders and neurodegenerative diseases. This coupling represents a fundamental organizing principle with significant therapeutic potential. Current challenges include developing quantitative methods for characterizing condensate dynamics in complex cellular environments and translating molecular mechanisms into clinical applications. Future progress requires interdisciplinary approaches combining advanced experimental techniques, computational modeling, and standardized protocols to advance both fundamental understanding and therapeutic innovations. Full article

Vacuum membrane-based air dehumidification (MAD) is potentially more efficient than refrigeration cycles. Air permeance through a membrane is inevitable, especially when there is a large pressure difference between the supply and permeate sides. Given the high specific gas volume under vacuum conditions, removing the permeating air from the dehumidifier is crucial for the stable operation of the vacuum compressor. Energy-efficient air removal techniques are still lacking, thereby hindering the development of MAD technology. This paper proposes a novel MAD approach using a vacuum mixing condenser. The cooling water directly condenses moisture from the vacuum compressor without any heat exchanger. The permeating air and water mixture in the condenser then experiences a quasi-isothermal pressurization process through a multiphase pump, enabling continuous dehumidification and air removal with low power consumption. The fundamentals of the proposed approach are illustrated, and mathematical models are built. Influences of air permeance rate, cooling water flow rate, condenser pressure, membrane area, and gravitational work are investigated. The results show that a COP of 8~12 is achievable to dehumidify air to 50%RH, 25 °C. The vacuum compressor consumes about 80% of the power. A low air permeance rate, low condenser pressure, large membrane area, and high gravitational work positively impact the COP, while the cooling water flow rate has a more complex effect. The proposed dehumidifier can use less selective membranes for higher permeability and cost-effectiveness. Full article

Membrane technology is widely used in gas separation processes due to its small footprint, high energy efficiency, and favorable economic viability. The current membrane market predominantly relies on polymer membranes, among which polyimide (PI) membranes stand out as highly promising materials due to their superior gas separation performance coupled with exceptional thermal and chemical stability. However, traditional polyimide membranes suffer from low gas permeability and insufficient plasticization resistance, hindering their broader industrial application. In order to meet the demands of more stringent application fields, it is crucial to further improve their gas performance and anti-plasticization to enhance their cost-effectiveness. Consequently, it is essential to modify traditional polyimides and formulate membrane fabrication strategies to solve these problems. This review introduces the monomer structures and synthesis approaches of polyimides, including solution-based and solid-state thermal condensation. Then, we propose representative preparation methods of polyimide-based membranes. Additionally, modification strategies, including thermal rearrangement, cross-linking, and physical blending, are summarized, which address the critical issues in contemporary polyimide-based gas separation membranes. Finally, this review critically discusses the current challenges and prospects for developing polyimide membranes for gas separation. Full article

Background/Objectives: The global increase in multidrug-resistant (MDR) bacterial infections underscores the urgent need for effective and sustainable antimicrobial alternatives. This study investigates the antimicrobial activity of exometabolite-based formulations (ExAFs), derived from the cell-free supernatants (CFS) of native lactic acid bacteria (LAB) applied individually or in combination thereof, against MDR-Escherichia coli strain L1PEag1. Methods: Fourteen ExAFs were screened for inhibitory activity using time–kill assays, and structural damage to bacterial cells was assessed via scanning and transmission electron microscopy (SEM/TEM). The most potent formulation was further characterized by liquid chromatography–tandem mass spectrometry (LC–MS/MS) employing a Sequential Windowed Acquisition of All Theoretical Fragment Ion Mass Spectra (SWATH) approach for untargeted metabolite profiling. Results: Among the tested formulations, E10, comprising CFS from Weissella cibaria UTNGt21O, exhibited the strongest inhibitory activity (zone of inhibition: 17.12 ± 0.22 mm), followed by E1 (CFS from Lactiplantibacillus plantarum Gt28L and Lactiplantibacillus plantarum Gt2, 3:1 v/v) and E2 (Gt28L CFS + EPS from Gt2, 3:1 v/v). Time–kill assays demonstrated rapid, dose-dependent bactericidal activity: E1 and E10 achieved >98% reduction in viable counts within 2–3 h, at 1× MIC, while E2 sustained 98.24% inhibition over 18 h, at 0.25× MIC. SEM and TEM revealed pronounced ultrastructural damage, including membrane disruption, cytoplasmic condensation, and intracellular disintegration, consistent with a membrane-targeting mode of action. Metabolomic profiling of E10 identified 22 bioactive metabolites, including lincomycin, the proline-rich peptide Val–Leu–Pro–Val–Pro–Gln, multiple flavonoids, and loperamide. Several compounds shared structural similarity with ribosomally synthesized and post-translationally modified peptides (RiPPs), including lanthipeptides and lassopeptides, suggesting a multifaceted antimicrobial mechanism. Conclusions: These findings position ExAFs, particularly E10, as promising, peptide-rich, bio-based antimicrobial candidates for food safety or therapeutic applications. The co-occurrence of RiPP analogs and secondary metabolites in the formulation suggests the potential for complementary or multi-modal bactericidal effects, positioning these compounds as promising eco-friendly alternatives for combating MDR pathogens. Full article

This study presents a detailed energy and exergy analysis of two forward osmosis (FO) desalination systems: single-pass and regenerative configurations. Both utilize osmotic pressure from a concentrated draw solution to drive water transport through a semi-permeable membrane. The regenerative system includes extra components for draw solute recovery, which increases electrical energy consumption to 188.9 kW and slightly lowers water recovery to 54%, compared to 98 kW and 60% for the single-pass FO system. Equivalent work for desalination is 1.4 kWh/m³ for single-pass and 1.8 kWh/m³ for regenerative FO systems. Exergy analysis shows the distillation column as the largest contributor to exergy destruction in both systems, responsible for over 44% of losses. The regenerative system adds 57.9 MW of chemical exergy destruction in the regenerator. Physical exergy destruction mainly occurs in the reboiler and condenser, while chemical exergy destruction is dominant in the FO membrane unit and regenerator. These findings provide valuable insights for improving the efficiency and sustainability of FO desalination technologies. Full article

Polymers and polymer composites offer versatile possibilities for engineering the physico-chemical properties of materials on micro- and macroscopic scales. This review provides an overview of polymeric and polymer-decorated particles that can serve as drug-delivery vectors: linear polymers, star polymers, diblock-copolymer micelles, polymer-grafted nanoparticles, polymersomes, stealth liposomes, microgels, and biomolecular condensates. The physico-chemical interactions between the delivery vectors and biological cells range from chemical interactions on the molecular scale to deformation energies on the particle scale. The focus of this review is on the structure and elastic properties of these particles, as well as their circulation in blood and cellular uptake. Furthermore, the effects of polymer decoration in vivo (e.g., of glycosylated plasma membranes, cortical cytoskeletal networks, and naturally occurring condensates) on drug delivery are discussed. Full article

An oxysterol, 25-Hydroxycholesterol (25OHChol), is produced through cholesterol oxidation and is involved in various cellular processes, including apoptosis. However, the precise mechanisms underlying 25OHChol-induced apoptosis in neuroblastoma cells remain unclear. The aim of this study was to elucidate the detailed molecular mechanisms by which 25OHChol induces apoptosis in human neuroblastoma cells. This study explores the apoptotic effects of 25OHChol and the associated signaling pathways in BE(2)-C cells, a widely used human neuroblastoma cell model for neuronal differentiation and cancer research. To evaluate the cytotoxicity of 25OHChol, cell viability was assessed using the CCK-8 assay, which demonstrated a concentration-dependent decline, indicating a potential induction of cell death. Morphological changes characteristic of apoptosis, such as nuclear condensation and fragmentation, were confirmed via DAPI staining. Additionally, Annexin V/PI flow cytometry analysis revealed an increase in late apoptotic cell populations, further corroborating apoptosis induction. To investigate the molecular mechanisms, we analyzed the expression of Bcl-2 family proteins via Western blotting. The results showed an elevated Bax/Bcl-2 ratio, suggesting activation of the intrinsic mitochondrial apoptotic pathway. This was further supported by a reduction in mitochondrial membrane potential (MMP), as measured by flow cytometry. Increased caspase-9 and caspase-3/7 activity provided additional evidence for caspase-mediated apoptosis. Moreover, treatment with the pan-caspase inhibitor Z-VAD-FMK led to a dose-dependent increase in cell viability, confirming the essential role of caspases in 25OHChol-induced apoptosis. In conclusion, this study demonstrates that 25OHChol triggers apoptosis in BE(2)-C neuroblastoma cells through activation of the intrinsic mitochondrial apoptotic pathway. These findings provide new insights into the cytotoxic effects of 25OHChol and its potential role in neuroblastoma cell death. Full article