Search Results (234)

Therapeutics involving small interfering RNA (siRNA) have enormous potential for treating a number of diseases, but their effective delivery to target cells remains a major challenge. We studied the influence of the structure and combination of targeted (folate conjugated, F13) and shield lipoconjugates (P1500, diP1500) on the ability of cationic liposomal formulations based on the 2X3-DOPE system to deliver siRNA into cells in vitro and in vivo. The loop-structured PEG lipoconjugate equipped with two hydrophobic anchor groups (diP1500) demonstrated superior performance across multiple evaluation criteria. The F13/diP1500 composition maintained a compact particle size (126.0 ± 23.0 nm), while F13/P1500 with the same PEG chain equipped with one anchor group maintained an increased particle size of 241.8 ± 65.7 nm. Most critically, F13/diP1500 preserved substantial positive surface charges (21.6–30.5 mV) across all N/P ratios, demonstrating superior ability in avoid the “PEG dilemma”, whereas F13/P1500 suffered substantial charge neutralization (3.9–9.1 mV). Competitive inhibition with free folate confirmed receptor-mediated cellular accumulation of siRNA mediated by F13 containing liposomal compositions. In vivo biodistribution revealed statistically significant circulation advantages: DSPE-PEG2000/diP1500 achieved the highest plasma concentration at 15 min (1.84 ± 0.01 pmol/mL), representing the first direct in vivo comparison of compositions with PEG lipoconjugates of the same length, but formed different structures in the liposomes due to the presence of one or two anchor groups. Our findings provide critical insights for the rational design of targeted liposomal delivery systems, highlighting the importance of balanced optimization between folate targeting functionality and PEG shielding for effective siRNA delivery both in vitro and in vivo. Full article

The evaluation of sperm proteins has emerged as a promising approach to predicting semen quality across animal species. This study investigated the relationship between post-thaw concentrations of precursor A-kinase anchor protein 4 (proAKAP4) and objective sperm quality parameters in goats. Semen was collected from 16 adult goats (Boer, n = 8; Anglo-Nubian, n = 8) and frozen using a standardized protocol with OptiXcell (IMV Technologies, l′Aigle, France) extender (n = 5). After thawing, proAKAP4 concentrations were measured with an enzyme-linked immunosorbent assay (ELISA), while sperm motility and kinematics were assessed with computer-assisted analysis (CASA), and viability, plasma membrane integrity, acrosome integrity, and mitochondrial activity were evaluated using flow cytometry. Samples were grouped according to low, medium, or high proAKAP4 levels for comparison, and correlations with sperm parameters were examined. The results showed that semen with higher proAKAP4 concentrations had significantly greater total and progressive motility, more favorable kinematic values, and improved viability, plasma membrane integrity, and mitochondrial function (p < 0.05), whereas acrosome integrity was not influenced (p > 0.05). The average post-thaw proAKAP4 concentration was 38.66 ± 1.11 ng/10⁶ sperm, and no differences were observed between Boer and Anglo-Nubian breeds (p > 0.05). These findings indicate that proAKAP4 is strongly associated with multiple sperm functional traits and may serve as a reliable biomarker for assessing post-thaw semen quality in goats. Full article

Background/Objectives: Glioblastoma (GBM) is an aggressive primary brain tumor with limited therapeutic options despite multimodal treatment. Small interfering RNA (siRNA)-based therapeutics can silence tumor-promoting genes, but achieving efficient and tumor-specific delivery remains challenging. Lipid nanoparticles (LNPs) are promising siRNA carriers; however, conventional antibody conjugation can impair antigen recognition and complicate manufacturing. This study aimed to establish a modular Fc-binding peptide (FcBP)-mediated post-insertion strategy to enable PD-L1-targeted delivery of VEGF-siRNA via LNPs for GBM therapy. Methods: Preformed VEGF-siRNA-loaded LNPs were functionalized with FcBP–lipid conjugates, enabling non-covalent anchoring of anti-PD-L1 antibodies through Fc interactions. Particle characteristics were analyzed using dynamic light scattering and encapsulation efficiency assays. Targeted cellular uptake and VEGF gene silencing were evaluated in PD-L1-positive GL261 glioma cells. Anti-tumor efficacy was assessed in a subcutaneous GL261 tumor model following repeated intratumoral administration using tumor volume and bioluminescence imaging as endpoints. Results: FcBP post-insertion preserved LNP particle size (125.2 ± 1.3 nm), polydispersity, zeta potential, and siRNA encapsulation efficiency. Anti-PD-L1–FcBP-LNPs significantly enhanced cellular uptake (by ~50-fold) and VEGF silencing in PD-L1-expressing GL261 cells compared to controls. In vivo, targeted LNPs reduced tumor volume by 65% and markedly suppressed bioluminescence signals without inducing weight loss. Final tumor weight was reduced by 63% in the anti-PD-L1–FcBP–LNP group (656.9 ± 125.4 mg) compared to the VEGF-siRNA LNP group (1794.1 ± 103.7 mg). The FcBP-modified LNPs maintained antibody orientation and binding activity, enabling rapid functionalization with targeting antibodies. Conclusions: The FcBP-mediated post-insertion strategy enables site-specific, modular antibody functionalization of LNPs without compromising physicochemical integrity or antibody recognition. PD-L1-targeted VEGF-siRNA delivery demonstrated potent, selective anti-tumor effects in GBM murine models. This platform offers a versatile approach for targeted nucleic acid therapeutics and holds translational potential for treating GBM. Full article

In response to the actual needs of pure copper bonding wires, it is crucial to develop a chromium-free passivator that is environmentally friendly and has excellent corrosion resistance. In this study, three different composite organic formulations of chromium-free passivation solutions are selected: 2-Amino-5-mercapto-1,3,4 thiadiazole (AMT) + 1-phenyl-5-mercapto tetrazolium (PMTA), 2-mercaptobenzimidazole (MBI) + PMTA, and Hexadecanethiol (CHS) + sodium dodecyl sulfate (SDS). The performance analysis and corrosion mechanism were compared with traditional hexavalent chromium passivation through characterization techniques such as XRD, SEM, and XPS. The results show that the best corrosion resistance formula is the combination of the PMTA and MBI passivation agent, and all its performances are superior to those of hexavalent chromium. The samples treated with this passivation agent corrode within 18 s in the nitric acid drop test, which is better than the 16 s for Cr⁶⁺ passivation. The samples do not change color after being immersed in salt water for 48 h. Electrochemical tests and high-temperature oxidation test also indicate better corrosion resistance than Cr⁶⁺ passivation. Through the analysis of functional groups and bonding, the excellent passivation effect is demonstrated to be achieved by the synergistic action of the chemical adsorption film formation of PMTA and the anchoring effect of MBI. Eventually, a dense Cu-PMTA-BMI film is formed on the surface, which effectively blocks the erosion of the corrosive medium and significantly improves the corrosion resistance. Full article

In this study, interface models of different polymer fibers and geopolymer products were constructed and the microscopic action mechanisms behind different polar oxygen-containing functional groups were revealed by analyzing the static structure of the interface and fiber pull-out process. The results show that, compared with polypropylene (PP) fibers, there is a strong hydrogen bond interaction in polyvinyl alcohol (PVA) and polyacrylic acid (PAA) fibers, respectively. After reaching equilibrium, the interlayer spacing of PVA and PAA fibers becomes smaller. At the interface, there are both ionic bonds and hydrogen-bonding connections, and the stability of ionic bonds is greater than that of hydrogen bonds. As the loading rate increases, the shear strength shows an increasing trend. Since the carboxyl of PAA fibers has stronger polarity than the hydroxyl of PVA fibers, the end deformation of the matrix is greater. During the pull-out process, the influence of the loading rate is greater than the anchoring effect of hydroxyl in PVA fibers but lower than that of carboxyl in PAA fibers. Full article

Lung adenocarcinoma (LUAD) remains the most common subtype of non-small-cell lung cancer and a major cause of cancer mortality, with many patients lacking actionable mutations or durable responses to targeted or immune therapies. Here, we report an integrative analysis of TCGA LUAD transcriptomes (n = 598) seeded from a curated ferroptosis gene catalogue, yielding a compact six-gene signature (AQP4, CDCA3, HJURP, KIF20A, PLK1, UHRF1) with diagnostic, prognostic, and therapeutic relevance. The signature was consistently dysregulated in tumours versus normal lung and stratified patients into high- and low-risk groups with distinct survival outcomes (log-rank p < 0.0001), outperforming conventional staging when incorporated into multivariable models. Across ten machine learning algorithms, the panel achieved near-perfect tumour-normal classification (AUC 0.99–1.00), highlighting its translational potential for early detection. Functional analyses linked the signature to cell-cycle, angiogenic, and immune modulation, while exploratory drug-gene correlations identified PLK1 and other candidates as potential therapeutic targets. Together, these findings establish a biologically anchored six-gene panel that complements existing mutation-based classifiers and provides a framework for advancing diagnostic precision, prognostic refinement, and biomarker-guided therapeutic strategies in LUAD. Full article

Modification of synthetic oligonucleotides and DNA is widely used in many applications in the life sciences. However, in most cases, modified DNA cannot be restored to its native state. Here, we report the preparation of a thymidine-inosine dimer building block (TID) for oligonucleotide synthesis. The TID modification supports the functionalization of synthetic oligonucleotides, which can later be removed to restore the DNA strand to its native state. The TID unit allows for a wide spectrum of postsynthetic modifications of oligonucleotides through click chemistry, including conjugation with fluorescent tags and small molecules, preparation of branched oligonucleotide scaffolds, and anchoring to a solid support. Due to the modification of the thymine base, the TID unit reduces the stability of the DNA duplex. We found that the negative effect of internal TID modification on duplex stability does not exceed the same for a single base mismatch. As long as the TID modification is present in the DNA strand, it disrupts its natural functionality. The “caging” effect of TID in the template strand with respect to DNA polymerase was demonstrated in primer extension experiments. Traceless removal of the temporary functional group occurs through oxidative cleavage of the inosine subunit, resulting in the formation of a native DNA strand with the thymine base left at the cleavage site. An anthracene-modified dodecamer oligonucleotide and a branched oligonucleotide scaffold were used to study the cleavage of the reporter group or the oligonucleotide side strand, respectively. It was shown that aqueous tetramethylguanidine efficiently cleaves the oxidized inosine subunit of TID at 37 °C, forming the native DNA strand. Full article

In this paper, a novel collector dihexyl (2-(hydroxyamino)-2-oxoethyl) phosphonate (DHHAOEP) was synthesized and used as a flotation collector to separate scheelite from quartz. Micro-flotation experiments demonstrated that DHHAOEP can effectively separate scheelite from quartz within a pH range of 6–9. Artificial mixed ores flotation experiments revealed that at a pH of approximately 8 and a DHHAOEP concentration of 8 × 10⁻⁵ mol/L, the flotation recovery of scheelite reached 73% with a grade of 54%. The contact angle and Zeta potential measurements showed that the addition of DHHAOEP caused a positive shift in the zeta potential and enhanced the surface hydrophobicity of scheelite. The FTIR, XPS, and DFT analyses further elucidated that DHHAOEP anchored on the scheelite surface through the bonding reaction between its -C(=O)-NHOH moiety and WO₄²⁻ or Ca active sites on the scheelite surface, forming a five-membered ring. Meanwhile, the existence of the P=O group makes the distance between oxygen atoms in -C(=O)-NHOH very close to that in WO₄²⁺, which is beneficial to the reaction. The present work aims to develop a novel flotation collector with multi-functional groups to enhance scheelite recovery efficiency and selectivity. Full article

In this study, a novel low-temperature (300–500 °C) carbothermal reduction route employing potassium ferrate and sodium hydroxide was developed to synthesize magnetic zero-valent iron-doped biochar for removing tetracycline and ciprofloxacin from aqueous solutions. Carbothermal reduction occurred effectively at 400 °C, generating sufficient small reductive molecules for the reduction of iron species into zero-valent iron. This process led to the impregnation of abundant zero-valent iron along with nano-magnetite into the carbon matrix, while nano-magnetite was also dispersed and stabilized on zero-valent iron. Simultaneously, abundant functional groups were formed, contributing to anchoring iron species and adsorbing pollutants. The magnetic biochar exhibited high adsorption capacities for tetracycline (1106.25 mg/g) and ciprofloxacin (182.03 mg/g), along with high saturation magnetization (56.3 emu/g) and superior reusability. Moreover, the magnetic biochar showed broad applicability for efficient removal of tetracycline and ciprofloxacin derivatives. Overall, carbothermal reduction efficiently transformed iron oxides into zero-valent iron at a relatively low temperature, providing a viable approach for manufacturing magnetic biochar doped with zero-valent iron. Full article

Lithium–iron disulfide (Li-FeS₂) batteries are plagued by the polysulfide shuttle effect and cathode structural degradation, which significantly hinder their practical application. This study proposes a dual-strategy design that combines a polyacrylonitrile–carbon nanotube (PAN-CNT) composite cathode and a polyvinylidene fluoride (PVDF)-conductive carbon-coated separator to synergistically address these bottlenecks. The PAN-CNT binder establishes chemical anchoring between polyacrylonitrile and FeS₂, enhancing electronic conductivity and mitigating volume expansion. Specifically, the binder boosts the initial discharge capacity by 35% while alleviating the stress-induced pulverization associated with volume changes. Meanwhile, the PVDF-conductive carbon-coated separator enables effective polysulfide trapping via dipole–dipole interactions between PVDF’s polar C-F groups and Li₂S_x species while maintaining unobstructed ion transport with an ionic conductivity of 1.23 × 10⁻³ S cm⁻¹, achieving a Coulombic efficiency of 99.2%. The electrochemical results demonstrate that the dual-modified battery delivers a high initial discharge capacity of 650 mAh g⁻¹ at 0.5 C, with a capacity retention rate of 61.5% after 120 cycles, significantly outperforming the control group’s 47.5% retention rate. Scanning electron microscopy and electrochemical impedance spectroscopy confirm that this synergistic design suppresses polysulfide migration and enhances interfacial stability, reducing the charge transfer resistance from 26 Ω to 11 Ω. By integrating polymer-based functional materials, this work presents a scalable and cost-effective approach for developing high-energy-density Li-FeS₂ batteries, providing a practical pathway to overcome key challenges in their commercialization. Full article

(1) Background: Virtual Reality (VR) films challenge traditional visual cognition by offering novel perceptual experiences. This study investigates the applicability of Gestalt grouping principles in dynamic VR scenes, the influence of VR environments on grouping efficiency, and the relationship between viewer experience and grouping effects. (2) Methods: Eye-tracking experiments were conducted with 42 participants using the HTC Vive Pro Eye and Tobii Pro Lab. Participants watched a non-narrative VR film with fixed camera positions to eliminate narrative and auditory confounds. Eye-tracking metrics were analyzed using SPSS version 29.0.1, and data were visualized through heat maps and gaze trajectory plots. (3) Results: Viewers tended to focus on spatial nodes and continuous structures. Initial fixations were anchored near the body but shifted rapidly thereafter. Heat maps revealed a consistent concentration of fixations on the dock area. (4) Conclusions: VR reshapes visual organization, where proximity, continuity, and closure outweigh traditional saliency. Dynamic elements draw attention only when linked to user goals. Designers should prioritize spatial logic, using functional nodes as cognitive anchors and continuous paths as embodied guides. Future work should test these mechanisms in narrative VR and explore neural correlates via fNIRS or EEG. Full article

To achieve dual functionality that can monitor both Al³⁺ levels in food and the freshness of fish, rice straw fibers (RSFs) were treated in NaOH solutions and then cationized with 2,3-epoxypropyltrimethylammonium chloride, onto which alizarin red S molecules were immobilized through electrostatic interaction to develop a smart felt-like label. An optimized treatment in 5 wt% NaOH solution effectively removed lignin and hemicellulose, facilitating quaternary ammonium group grafting and stable ARS anchoring. The ARS@BRSF-5NaOH exhibited high pH sensitivity, showing visually discernible color changes (ΔE > 5, perceptible to the naked eye) under acidic (pH ≤ 6) and strongly alkaline (pH > 12) conditions. During the storage of the fish, the label transformed from yellow to dark purple (ΔE increase) as TVB-N levels approached 20 mg/100 g, enabling real-time freshness monitoring for protein-rich products. Additionally, the label achieved a detection threshold of 1 × 10⁻⁵ mol·L⁻¹ for Al³⁺ through a coordination-induced chromatic transition (purple to pale pink). This research highlights the feasibility of utilizing an agricultural waste-derived material to develop cost-effective, visually responsive, dual-functional intelligent labels for food safety, offering significant advancements in on-site quality assessment. Full article

Aryl diazonium salt chemistry offers a robust and versatile approach for the modification of material surfaces via the covalent immobilization of reactive functional groups under mild conditions. In this study, this strategy was successfully applied to graft the chelating agent 4-(2-pyridylazo)resorcinol (PAR) onto Amberlite XAD-4 resin. Initially, 4-nitrobenzenediazonium tetrafluoroborate (NBDT) was covalently anchored onto the resin surface using hypophosphorous acid as a reducing catalyst to introduce aryl nitro groups. These nitro groups were subsequently reduced to aniline functionalities, enabling diazo coupling with PAR. The successful modification of the resin was confirmed by ATR-FTIR spectroscopy, thermogravimetric analysis (TGA), and X-ray photoelectron spectroscopy (XPS). The synthesized chelating resin exhibited sorption capacities of 0.152, 0.167, and 0.172 mM g⁻¹ for Co(II), Ni(II), and Cu(II), respectively. The functionalized resin was packed into standard SPE cartridges and employed as a selective sorbent for the extraction and preconcentration of trace metals from groundwater samples collected from Dhalamah Valley, Al-Madinah Al-Munawwarah, prior to quantification by inductively coupled plasma mass spectrometry (ICP-MS). These results demonstrate the effectiveness of rapid diazonium-based surface functionalization for the preparation of selective polymeric metal chelators suitable for the extraction of trace metals from complex groundwater matrices. Full article

The conversion of cellulosic biomass into renewable chemicals can serve as a sustainable resource for levulinic acid (LA) production. LA yield is significantly influenced by reaction temperature, reaction time, substrate concentration, active sites, catalyst amount, catalyst porosity, and durability. Beyond the features of the catalyst, such as acidity, porosity, functional groups, and catalytic efficiency, the contact between the solid acid catalyst and the solid substrate is of vital importance. Solid-based catalysts show remarkable catalytic activity for cellulose-derived LA production, thanks to the incorporation of functional groups. For a solid carbon-based catalyst to be effective, a synergistic interaction between the binding domain (functional groups capable of anchoring cellulose to the catalyst surface, such as chloride groups, COOH, or OH) and the hydrolysis domain (due to their ability to cleave glycosidic bonds, such as in SO₃H) is essential. As a relatively new market niche, carbon-based catalyst supports are projected to reach a market value of nearly USD 125 million by 2030. This review aims to highlight the advantages and limitations of carbon-based materials compared to conventional catalysts (including metal oxides or supported noble metals, among others) in features like catalytic activity, thermal stability, and cost, examine recent advancements in catalyst development, and identify key challenges and future research directions to enable more efficient, sustainable, and scalable processes for LA production. The novelty of this review lies in its focus on carbon-based catalysts for LA production, emphasizing their physical and chemical characteristics. Full article

To address the issue of drilling fluid performance drop and wellbore instability induced by desorption between treatment agents and clay in the high-temperature environment of ultra-deep drilling, this study synthesized three organosilicon polymers (ADE, ADM, ADD) with different substituents. The study confirmed that the covalent bond significantly improved the high-temperature adsorption resistance of clay, which is closely related to the interface behavior of gels. Through rolling recovery, rheology, and filtration experiments for performance evaluation, these organic silicon polymers showed excellent high-temperature performance: the shale rolling recovery rate exceeded 80% at 210 °C, and the filtration loss was reduced to 14 mL, with a reduction rate of 53.3%. The adsorption capacity of the three polymers on clay remained unchanged from 150 °C to 210 °C, among which the adsorption amount of trimethoxy groups stabilized at 8–11 mg/g after 150 °C. The adsorption capacity of ethoxy groups increased by 7.9% at 150–210 °C. The adsorption capacity of dimethoxy groups with methyl steric hindrance increased by 28.1% at 150–210 °C. These results indicate that covalent bonds effectively enhance the high-temperature adsorption of clay, allowing for polymer molecules to firmly anchor on the clay surface at high temperatures. This breakthrough overcomes the limitations of traditional inhibitors in high-temperature desorption, and provides a valuable reference for the preparation of high-temperature adsorption resistant functional materials in water-based drilling fluid gel systems. Full article