Search Results (1,211)

To address the low energy conversion efficiency and weak mechanical strength of In₂O₃ thermoelectric materials for Aiye Processing Equipment, this study systematically investigated the regulatory effects and mechanisms of Ce doping on In₂O₃’s thermoelectric and mechanical properties via experiments. In₂O₃ samples with varying Ce contents were prepared, and property-microstructure correlations were analyzed through electrical/thermal transport tests, Vickers hardness measurements, and crystal structure characterization. Results show Ce doping synergistically optimizes In₂O₃ properties through multiple mechanisms. For thermoelectric performance, Ce⁴⁺ regulates carrier concentration and mobility, enhancing electrical conductivity and power factor. Meanwhile, lattice distortion from Ce-In atomic size differences strengthens phonon scattering, reducing lattice and total thermal conductivity. These effects boost the maximum ZT from 0.055 (pure In₂O₃) to 0.328 at 973 K obtained by x = 0.0065, improving energy conversion efficiency significantly. For mechanical properties, Ce doping enhances Vickers hardness and plastic deformation resistance via solid solution strengthening (lattice distortion hinders dislocations), microstructure densification (reducing vacancies/pores), Ce-O bond strengthening, and defect pinning. This study confirms Ce doping as an effective strategy for simultaneous optimization of In₂O₃’s thermoelectric and mechanical properties, providing experimental/theoretical support for oxide thermoelectric material development and valuable references for their medium-low temperature energy recovery applications. Full article

This study presents an energy-efficient, room-temperature synthesis and characterization of methacrylated pullulan (Pull-MA) hydrogel developed for controlled nutrient delivery in agricultural applications. Fourier Transform Infrared Spectroscopy (FTIR) and Differential Scanning Calorimetry (DSC) analyses confirmed the successful functionalization of pullulan with methacrylate groups, accompanied by a decrease in thermal transition temperatures, indicative of increased polymer chain mobility. The synthesized Pull-MA hydrogel exhibited a high swelling capacity, reaching an equilibrium swelling ratio of 1068% within 5 h, demonstrating its suitability as a carrier matrix. The room-temperature synthesis approach enabled the in situ incorporation of microbial inoculant into the hydrogel network, preserving microbial viability and activity. SEM analysis performed under the different magnifications (1000, 2500, 5000, 10,000, 25,000×) has confirmed brittle nature of xerogels and increasing in structural irregularities with increasing in cultivation broth content.The biological performance of the fertilizer-loaded hydrogels was evaluated through seed germination assays using maize and pepper as model crops. The optimized formulation, T2 (Pull-MA: cultivation broth 1:5 w/w), significantly improved germination efficiency, as evidenced by increased relative seed germination (RSG), root growth rate (RRG), and germination index (GI) compared to both the control and the low-fertilizer formulation (T1, 1:2.5 w/w). These findings highlight the potential of Pull-MA hydrogels as bioactive seed-coating materials that enhance early seedling development through controlled nutrient release. The results lay a solid foundation for further optimization and future application of this system under real field conditions. Full article

The leather industry generates large amounts of solid waste, creating environmental concerns for the presence of hazardous compounds such as chromium. In fact, conventional disposal practices, including landfill and incineration, promote the formation of hexavalent chromium (Cr⁶⁺) and polluting emissions. This work reviews biochemical and thermochemical processes for the energetic valorization of different leather solid wastes, namely untanned, tanned with chromium or vegetable tanning agents, and post-consumer leather. Thermochemical routes, i.e., pyrolysis, gasification, and hydrothermal treatment (HT), can convert leather waste into energy carriers including bio-oil, syngas, and char, while anaerobic digestion (AD) is a biochemical method used to produce biogas. Particularly, pyrolysis is promising for fuel precursors and chromium stabilization, HT suits wet, raw waste, while gasification enables syngas recovery. In AD, microbial chromium inhibition is mitigated through the co-digestion of degradable substrates. This review takes a waste-type-driven rather than process-driven approach to provide new insights into the conversion of leather solid waste into value-added products, showing that the optimal recycling route depends on the waste characteristics. Moreover, these methods have not yet been directly compared in terms of their energy production performance with regard to leather waste. Future work should improve process conditions, evaluate chromium and finishing additive impacts, and assess scalability. Full article

Drill pipe pullback gravel packing is a novel sand control method for marine natural gas hydrate reservoirs, enabling rapid and uniform filling by synchronizing fluid injection with pipe retraction. However, the complex liquid–solid two-phase flow mechanisms and parameter sensitivities in this dynamic process remain unclear. To address this gap, a coupled Computational Fluid Dynamics and Discrete Element Method (CFD-DEM) approach is adopted in accordance with the trial production requirements in the South China Sea. This investigation systematically analyzes the relative contributions of injection rate (0.8–2.2 m³/min) and sand-carrying ratio (30–60%) to the packing effectiveness. Additionally, the effects of carrier fluid viscosity and drill pipe pullback speed are explored. Results show that injection rate and sand-carrying ratio positively affect performance, with sand-carrying ratio as the decisive factor, exhibiting an impact approximately 73 times greater than that of the injection rate. Optimal parameters in this study are injection rate of 2.2 m³/min and sand-carrying ratio of 60%, which yield the highest gravel volume fraction and stable bed height. Furthermore, it is also found that while increasing carrier fluid viscosity improves bed height, excessive viscosity hinders particle settling and compaction. Similarly, a trade-off exists for the pullback speed to balance packing density and pipe burial risks. These findings provide a theoretical basis for optimizing sand control operations in hydrate trial productions. Full article

The present study aimed to design a process of brown onion skin transformation by sequential extraction to a cellulose-based immobilization carrier, along with detailed analysis of obtained extracts, pointing to approaching a “zero-waste” model of circular economy. The process of brown onion skin transformation started with semi-continuous sequential subcritical extraction via consecutive use of five solvents of increasing polarity (96, 75, 50, and 25% ethanol and water), followed by alkaline liquefaction of solid residue by 10% aqueous solution of sodium hydroxide. The designed BOS transformation process resulted in 16.62 g of cellulose-based immobilization carrier derived from 100 g of brown onion skin. Extracts obtained by semi-continuous sequential subcritical extraction contained 37 mg/g of proteins, 40 mg/g of sugars, 17.5 mg/g of uronic acids, 28 mg/g of polyphenols, and 36 mg/g of flavonoids, while those obtained by alkaline liquefaction 19 mg/g of proteins, 58 mg/g of sugars, 10 mg/g of uronic acids, 6.6 mg/g of polyphenols, and 0.5 mg/g of flavonoids. The suitability of the cellulose-based enzyme immobilization carrier was evaluated by B. cepacia lipase immobilization by adsorption, where a maximal 31 U of lipase activity per 1 g of wet carrier was achieved. Based on the results obtained, it seems that the proposed process of brown onion skin transformation shows the possibility of being used for the production of a cellulose-based immobilization carrier, approaching the “zero-waste” model of a circular economy. Full article

Acyl-CoA-binding proteins (ACBPs) are essential lipid carrier proteins involved in plant lipid metabolism. However, the systematic identification and expression profiles of the ACBP gene family in citrus species remain poorly understood. Here, Citrus sinensis and Poncirus trifoliata were chosen as model species to examine the biological properties of citrus ACBPs. Using bioinformatics methods, five ACBP gene members were found in each species and named CsACBPs and PtrACBPs, respectively. All obtained ACBP members were divided into four subfamilies based on conserved domains and amino acid sequences. CsACBP and PtrACBP genes exhibited structural variation in motifs and exons. The predicted protein structures of CsACBPs and PtrACBPs exhibited conservation between the two species while displaying distinct variation within each species. Collinearity analysis showed one intraspecific pairing relationship in each of the two citrus species. Furthermore, there were more collinear couplings between citrus species and Arabidopsis thaliana but none between citrus species and Oryza sativa (rice). Notably, the analysis of cis-acting elements in ACBP gene promoters identified a number of motifs associated with light, abiotic stresses, and phytohormones. Expression profiling confirmed tissue-specific expression patterns of CsACBP1~5 and PtrACBP1~5. RT-qPCR analysis revealed that all CsACBP and PtrACBP genes responded to cold and salt stresses, though the magnitude of their responses varied significantly. Specially, although PtrACBP5 did not respond to low temperatures as rapidly as other members, its expression level increased significantly after 24 h of low-temperature treatment. Protein–protein interaction (PPI) network predictions indicated tight associations among four of the five CsACBPs, with CsACBP5 excluded from these interactions. Moreover, CsACBP1, CsACBP2, and CsACBP3 were predicted to be potential targets of csi-miR3952, csi-miR396a, and csi-miR477b, respectively. Overall, our research provides a solid foundation for further investigations into the biological functions and regulatory mechanisms of ACBP genes in citrus growth, development, and stress adaptation. Full article

Diroximel fumarate (DRF) is an orally administered prodrug used in multiple sclerosis (MS) treatment. Although it exhibits better gastrointestinal (GI) tolerability than its analogues, many patients still discontinue therapy due to frequent GI adverse events. To overcome these limitations, alternative drug delivery systems that bypass the GI tract are needed. Direct nose-to-brain delivery represents a promising approach to circumvent the blood–brain barrier and target the central nervous system; however, limited nasal mucosal absorption and the small volume of the nasal cavity pose significant challenges. Solid lipid nanoparticles (SLNs) can potentially overcome these obstacles by enhancing drug bioavailability and protecting against enzymatic degradation. This research aimed to develop an innovative intranasal nanoformulation of DRF to improve brain targeting and patient compliance. DRF-loaded SLNs were prepared using a solvent-diffusion technique with stearic acid as the lipid phase and Poloxamer 188 as the surfactant. The obtained nanoparticles displayed favorable technological characteristics, with a mean diameter of 210 nm, a polydispersity index of 0.17, and a zeta potential of −36 mV, suggesting good long-term stability. Interactions between SLNs and biomembrane models (MLV) were also studied to elucidate their cellular uptake mechanism. Future work will focus on evaluating the in vivo efficacy of this novel nanoformulation. Full article

Background/Objectives: Rutin, a bioactive flavonol glycoside known for its antioxidant, anti-inflammatory, and anticancer activities, faces limited clinical application due to its poor aqueous solubility and low oral bioavailability. This study aimed to enhance the dissolution of rutin by preparing solid dispersions (SDs) using a fluid-bed coating system and formulating the resulting SDs into tablet dosage forms. Methods: Rutin was dissolved in methanol and sprayed onto various carriers, including lactose monohydrate, mannitol, microcrystalline cellulose, silicon dioxide, and calcium carbonate. Results: Among the carriers tested, lactose monohydrate produced the highest dissolution enhancement, achieving complete drug release within 15 min versus approximately 60% for free rutin. Further investigation into the effect of the rutin-to-lactose ratio on dissolution enhancement identified 1:10 as the most effective. Characterization by powder X-ray diffraction (PXRD) and differential scanning calorimetry (DSC) confirmed a marked reduction in rutin crystallinity, while scanning electron microscopy (SEM) revealed reduced particle size and successful adsorption onto the carrier. Fourier transformed infrared (FT-IR) analysis suggested hydrogen bonding interactions between rutin and lactose monohydrate, which contributed to improved dissolution. The optimal SD was incorporated into tablets containing 50 mg of rutin via wet granulation, and the inclusion of sodium lauryl sulfate further enhanced dissolution. Stability testing demonstrated that the optimized tablets maintained their dissolution profile after 6 months under accelerated conditions (40 °C and 75% RH). Conclusions: These findings indicate that fluid-bed coating is an effective approach for preparing SDs to improve the dissolution of rutin and may be extended to other natural polyphenolic compounds. Full article

Background: Amelanchier alnifolia (Juneberry) is a phenolic-rich species with potential for pharmaceutical applications. This study aimed to optimize ultrasound-assisted extraction (UAE) conditions for producing ethanolic extracts from differently processed Juneberry berries collected in Lithuania and to develop solid oral dosage forms based on the obtained extracts. Methods: Extracts were prepared using varying ethanol concentrations, temperatures, and extraction times from dried, frozen, and freeze-dried berries. Total phenolic content (TPC) and total flavonoid content (TFC) were determined spectrophotometrically. Antioxidant activity was evaluated by DPPH and ABTS assays. Phenolic profiles were quantified by high-performance liquid chromatography (HPLC), identifying five major compounds. Extracts were converted into powders using lactose monohydrate, microcrystalline cellulose, or magnesium aluminum metasilicate as carriers. Hard capsules were manufactured and evaluated according to European Pharmacopoeia (Ph. Eur.) requirements, including mass uniformity, moisture content, and disintegration time. Results: Freeze-dried berries yielded the highest TPC, TFC, and antioxidant activity across all extraction conditions. The most efficient extraction parameters for freeze-dried berries were identified as 50% ethanol, 50–55 °C, and 30 min. HPLC analysis confirmed the presence of chlorogenic and neochlorogenic acids, rutin, hyperoside, and isoquercitrin. Among the powdered systems, lactose monohydrate demonstrated favorable flowability and moisture characteristics. Conclusions: Freeze-dried Juneberry berries are a suitable raw material for producing phenolic-rich extracts with strong antioxidant activity. Lactose-based powder blends showed the best technological performance and were successfully formulated into hard capsules. These findings support the potential of Juneberry extracts for incorporation into standardized pharmaceutical dosage forms and provide a basis for future formulation and bioavailability studies. Full article

Optimizing copper recovery from sulfide minerals such as chalcopyrite, which constitutes over 70% of global copper reserves, is essential due to the depletion of conventional copper oxide resources. This study aimed to establish optimal ferric leaching conditions for a chalcopyrite-rich concentrate to maximize copper recovery and to evaluate the regeneration of the oxidizing potential in the residual leaching solution for reuse. Ferric sulfate (Fe₂(SO₄)₃), as a ferric ion (Fe³⁺) carrier, was used as oxidizing agents at a concentration of [0.1 M] in sulfuric acid ([0.5 M] H₂SO₄), using a CuFeS₂ concentrate (75% chalcopyrite) leached over 80 h. Copper was recovered through cementation with metallic iron, while the residual leaching solution, containing ferrous ions, was analyzed to determine total iron content via atomic absorption spectroscopy and to assess the presence of ferrous ions through KMnO₄ titration. This step was crucial, as an excess of ferrous ions would indicate a loss of oxidizing potential of the ferric ion (Fe³⁺). Catalytic oxidation was conducted with microporous activated carbon (30 g/L) to regenerate Fe³⁺ for a second leaching cycle, achieving 90.7% Fe²⁺ oxidation. Optimal leaching conditions resulted in 95% soluble copper recovery at 1% solids, d80: 74 μm, pH < 2, Eh > 450 mV, 92 °C, [0.5 M] H₂SO₄, and [0.1 M] Fe₂(SO₄)₃. In the second cycle, the regenerated solution reached 75% copper recovery. These findings highlight temperature as a critical factor for copper recovery and demonstrate catalytic oxidation as a viable method for regenerating ferric solutions in industrial applications. Full article

Background: Penfluridol is a long-acting oral antipsychotic used for the treatment of schizophrenia. Although the prolonged half-life of penfluridol allows once-weekly dosing, improving patient compliance, its therapeutic potential is limited by low aqueous solubility and poor oral absorption. This study aimed to enhance the dissolution and oral bioavailability of penfluridol using solid dispersion technology. Methods: Ternary solid dispersions of penfluridol were prepared using a solvent evaporation method with various hydrophilic carriers. Following prescreening of polymeric carriers, the formulation composition was optimized using a random forest regression model. Structural characteristics and drug release behavior of the optimized formulation (PF-SD5) were evaluated through in vitro studies. Pharmacokinetic studies in rats were conducted to assess the effectiveness of PF-SD5 in enhancing oral bioavailability. Results: The optimized PF-SD5 formulation, comprising penfluridol, poloxamer 407, and polyvinylpyrrolidone K30 in a 1:3:1 ratio, exhibited a 117-fold increase in aqueous solubility compared with the pure drug. PF-SD5 achieved nearly complete drug release within 1 h across a pH range from acidic to neutral. Spectroscopic, microscopical, and thermal analyses confirmed that penfluridol transformed into an amorphous form and established molecular interactions within the carrier matrix. Pharmacokinetic studies in rats revealed approximately a 1.9-fold increase in oral bioavailability. Conclusions: Combining solid dispersion technology with machine learning-guided optimization provides an effective strategy for enhancing the oral absorption of poorly soluble penfluridol. Full article

Background/Objectives: Surfactants are commonly used in amorphous solid dispersions (ASDs) to improve drug dissolution. A mechanistic understanding of their impact on in vitro dissolution and in vivo pharmacokinetics is essential for rational ASD design and for establishing predictive in vitro–in vivo correlation (IVIVC). Methods: Binary (Cur/P188) and ternary (Cur/P188/TW80, Cur/P188/SLS) ASDs were prepared by rotary evaporation. Drug–polymer–surfactant interactions were characterized by ¹H NMR and FT-IR spectroscopy. To elucidate the bioavailability enhancement mechanism, we performed (i) in vitro non-sink dissolution to assess dissolution kinetics, nanostructure formation, and precipitate transformation; (ii) cellular uptake assays; and (iii) in vivo pharmacokinetic studies. Results: Cur self-associates via hydrogen bonding and π-π stacking, limiting its solubility. Polymer carrier P188 disrupts these interactions and forms stronger drug–polymer bonding. Surfactants TW80 and SLS exhibited distinct interaction profiles: TW80 competitively disrupted Cur-P188 bonding, whereas SLS integrated into the Cur-P188 assembly to form stable ternary nanostructures. The Cur/P188/SLS ASD achieved the highest and most sustained supersaturation, maintained amorphous precipitates, and enhanced cellular uptake, leading to significantly improved oral bioavailability. Conclusions: Surfactants critically influence ASD performance by preserving high-energy drug states through three key mechanisms: (1) generating and maintaining supersaturation, (2) facilitating nanostructure formation, and (3) stabilizing amorphous precipitates. These mechanisms collectively enhance cellular uptake and bioavailability. Our findings demonstrate that both dissolution and in vivo performance are governed by multifaceted drug–polymer–surfactant interactions, providing critical insights into surfactant functionality and IVIVC to guide rational ASD formulation. Full article

Constructing two-dimensional (2D) novel materials using superatoms as building blocks is currently a highly promising research field. In this study, by employing an oxidation strategy and based on first-principles calculations, we successfully predicted two types of 2D borides, namely B₁₂X₂H₆ (X=O, S), with icosahedral B₁₂ serving as their core structural unit. Ab initio molecular dynamics simulations demonstrated that these two borides exhibit exceptionally high structural stability, retaining their original structural characteristics even under extreme temperature conditions as high as 2200 K. Electronic structure calculations revealed that B₁₂O₂H₆ and B₁₂S₂H₆ are both wide-bandgap indirect semiconductors, with bandgap widths reaching 4.92 eV and 5.25 eV, respectively. Analysis via deformation potential theory showed that the phonon-limited carrier mobilities of B₁₂X₂H₆ can reach up to 1469 cm²V⁻¹s⁻¹ (for B₁₂O₂H₆) and 635 cm²V⁻¹s⁻¹ (for B₁₂S₂H₆). Notably, the surfaces of B₁₂X₂H₆ demonstrate excellent migration performance for alkali metal ions, with migration barriers as low as 0.15 eV (for B₁₂O₂H₆) and 0.033 eV (for B₁₂S₂H₆). This study not only expands the family of 2D materials based on B₁₂ superatoms but also provides a solid theoretical foundation for the potential application of B₁₂X₂H₆ in the field of low-dimensional materials. Full article

Polymeric semiconductors have rapidly evolved from early conductive polymers, such as polyacetylene, to high-performance donor–acceptor copolymers, offering a unique combination of mechanical flexibility, solution processability, and tunable optoelectronic properties. These advancements have positioned polymeric semiconductors as versatile materials for next-generation electronics, including wearable, stretchable, and bio-integrated devices, IoT systems, and soft robotics. In this review, we systematically present the fundamental principles of polymeric semiconductors, including electronic structure, charge transport mechanisms, molecular packing, and solid-state morphology, and elucidate how these factors collectively govern device performance. We further discuss recent advances in synthesis strategies, thin-film processing techniques, molecular doping, and interface engineering, emphasizing their critical roles in improving operational stability, charge-carrier mobility, and energy efficiency. Key applications—such as organic photovoltaics, field-effect transistors, neuromorphic devices, and memristors—are analyzed, with a focus on the intricate structure–property–performance relationships that dictate functionality. Finally, we highlight emerging directions and scientific innovations, including sustainable and degradable polymers, hybrid and two-dimensional polymer systems, and novel strategies to enhance device stability and performance. By integrating fundamental polymer science with device engineering, this review provides a comprehensive, structured, and forward-looking perspective, identifying knowledge gaps and offering insights to guide future breakthroughs and the rational design of high-performance, multifunctional, and environmentally responsible polymeric electronic devices. Full article

Sinomenine (SIN), as a potential therapeutic agent for rheumatoid arthritis (RA), exhibits advantages such as non-addictiveness. However, its low aqueous solubility and poor membrane permeability result in limited bioavailability, which compromises its therapeutic efficacy in conventional formulations. To address these limitations, this study developed nanostructured lipid carriers (NLCs) with optimized formulations and evaluated their pharmacodynamic performance. Molecular dynamics (MD) simulations were employed to screen excipients and analyze the blending system. SIN-loaded NLCs (SIN-NLCs) were prepared using high-pressure homogenization. Single-factor experiments were performed to optimize the processing conditions of SIN-NLCs. A three-factor, three-level experimental design was established using Design Expert 13 software and further refined through Box–Behnken design (BBD) response surface methodology. This approach enabled cross-validation between molecular dynamics simulations and conventional experiments. Additionally, transmission electron microscopy (TEM) was used to examine morphology, while X-ray diffraction analysis (XRD), differential scanning calorimetry (DSC), and Fourier-transform infrared spectroscopy (FT-IR) were employed to characterize the physicochemical state of SIN in NLCs. Pharmacodynamic evaluation was performed in a RA model, supplemented by single-pass intestinal perfusion study (SPIP). Initially, MD simulations were employed to evaluate drug–excipient compatibility, thereby identifying suitable formulation excipients: stearic acid and oleic acid as lipid components, and Poloxamer 188 as the surfactant. Subsequently, single-factor experiments combined with the BBD response surface methodology were employed to optimize preparation parameters, establishing the ideal process conditions: drug-to-lipid ratio of 1:42, solid-to-liquid lipid ratio of 5.58:4.42, and Poloxamer 188 concentration of 1.20%. The optimized SIN-NLCs exhibited spherical particles with uniform dispersion and no agglomeration. The average particle size was 173.90 ± 1.97 nm, with a polydispersity index (PDI) of 0.18 ± 0.01, a zeta potential of −22.65 ± 0.60 mV, and an encapsulation efficiency (EE%) of 91.27% ± 0.01. Spectroscopic analysis confirmed that SIN existed in an amorphous state and was successfully encapsulated within the lipid matrix. In vivo, SIN-NLCs significantly reduced paw swelling and arthritis scores in model rats, promoted synovial cell proliferation, and suppressed inflammatory cell infiltration. The intestinal perfusion study demonstrated that SIN-NLCs were primarily absorbed in the small intestine and markedly enhanced drug permeability. SIN-NLCs represent an effective delivery system to enhance the solubility and permeability of SIN. This study provides a novel strategy and methodology for the formulation of hydrophobic drugs, offering valuable insights for future pharmaceutical development. Full article