Search Results (4,895)

This work investigates the reactive crystallization of lithium carbonate (Li₂CO₃) by rapidly mixing concentrated aqueous solutions of LiCl (3.0–4.0 M) and Na₂CO₃ (1.5–2.0 M) at 65 °C, using focused beam reflectance measurement (FBRM) for online, in situ monitoring. The effect of low concentrations of poly(acrylic acid) (PAA), sodium hexametaphosphate (SHMP), and sodium tripolyphosphate (STPP) on nucleation and growth dynamics was systematically analyzed. The results show that the process is dominated by an intense initial supersaturation pulse, which governs early nucleation and subsequent population restructuring through growth and aggregation. Additives significantly modify the nucleation-growth coupling: PAA exhibits concentration- and time-dependent behavior, suppressing the detectable fines population and promoting consolidation into coarse fractions under high supersaturation; SHMP acts as a strong kinetic inhibitor, markedly reducing nucleation and, to a greater extent, growth; while STPP exhibits an intermediate, dose-dependent response, maintaining nucleation but limiting effective growth at high concentrations. Scanning electron microscopy observations confirm the formation of spherulitic Li₂CO₃ aggregates in all cases, with compactness and radial organization dependent on the additive. These results demonstrate that targeted additive selection allows for precise control of population dynamics and solid properties in reactive crystallization systems, within the investigated high-supersaturation concentration window, with useful mechanistic guidance for the design and control of Li₂CO₃ precipitation processes. Full article

Ovarian cancer progression is strongly influenced by tumour hypoxia and associated oxidative stress. Experimental evidence indicates that cysteine availability supports ovarian cancer cell fitness under hypoxic conditions, yet the quantitative integration of cysteine metabolism, redox control, and energetic maintenance remains incompletely understood. We present a reduced mechanistic mathematical model describing intracellular cysteine allocation between glutathione (GSH) synthesis and hydrogen sulfide production under experimentally imposed hypoxia. The model integrates extracellular cysteine uptake, GSH-dependent reactive oxygen species (ROS) detoxification, hypoxia-amplified ROS generation, and redox-modulated ATP maintenance. Parameter estimation was performed using experimentally derived extracellular metabolite fluxes measured over a 24 h interval. Uncertainty was assessed via bootstrap resampling, and variance-based sensitivity analysis was conducted within (patho)physiologically constrained parameter domains. The calibrated model reproduces extracellular fluxes with relative deviations below 7% and identifies GSH synthesis capacity as the dominant determinant of ATP maintenance within experimentally supported ranges. Hydrogen sulfide (H₂S) production exerts a secondary stabilising influence, whereas hypoxia-driven ROS amplification negatively impacts energetic state. Numerical continuation across hypoxia levels reveals distinct qualitative response regions but does not imply a formal bifurcation structure. Importantly, intracellular metabolite dynamics are inferred as latent variables consistent with extracellular constraints and established biochemical knowledge; the model does not uniquely identify intracellular pool sizes or enzyme kinetics. The framework therefore provides flux-consistent mechanistic plausibility rather than direct intracellular validation. This systems-level analysis supports cysteine allocation as a quantitatively influential control point in hypoxic adaptation and establishes a constrained modelling framework for subsequent metabolic network expansions and experimental validation. Full article

Amyloidosis is characterized by the deposition of misfolded proteins as highly stable, insoluble β-sheet-rich fibrils, posing a major therapeutic challenge due to their resistance to degradation. Insulin-derived amyloidosis at subcutaneous injection sites is a clinically significant complication in patients with diabetes, leading to impaired insulin absorption, unpredictable glycemic control, substantially increased insulin dose requirements, and localized masses (amyloidomas) that may require surgical excision when symptomatic. In this study, we evaluated sodium oleate-functionalized magnetic nanoparticles (MNs) with a hydrodynamic diameter of 50 nm with a magnetite (iron oxide—Fe₃O₄) core as a targeted physical intervention to disrupt preformed insulin amyloid fibrils. The strategy exploits localized nanoscale hyperthermia generated by MNs under a high-frequency radiofrequency (RF) field (1.65 MHz). Fibril integrity and disassembly kinetics were assessed using Thioflavin T (ThT) fluorescence assays and fluorescence microscopy. RF-activated MNs induced rapid, concentration-dependent fibril disruption; notably, at 2 mg/mL MNs, near-complete disassembly was achieved within 15 min—a timeframe compatible with clinical procedures. Neither RF nor MNs alone produced significant effects, confirming a synergistic magnetothermal mechanism. These results provide a proof of concept for a minimally invasive, externally triggered approach to clear localized insulin amyloid deposits, offering promising potential as a novel therapeutic strategy for managing injection-site amyloidosis in diabetic patients, where current options remain limited and often inadequate. Full article

We investigated the effects of atmospheric-pressure plasma treatment on the growth of Saccharomyces cerevisiae by directly comparing plasma exposure and plasma-activated medium (PAM) under strictly identical discharge conditions. An atmospheric-pressure plasma jet operated with argon (Ar) or nitrogen (N₂) was used. Yeast growth was analyzed using a phase-resolved kinetic framework that separately evaluated early growth behavior and exponential growth rate based on optical density measurements. Growth curves were normalized to same-day untreated controls to minimize day-to-day variability. Under N₂ plasma conditions, both direct exposure and PAM treatment resulted in limited changes in growth kinetics (μ_rel = 0.67–0.97; t_rel ≈ 1.02–1.09). In contrast, Ar plasma treatment produced clear mode-dependent effects. Direct exposure delayed growth initiation (t_rel = 1.00–1.40) with a moderate reduction in μ_rel (0.63–0.84). PAM treatment strongly suppressed μ_rel (0.19–0.50), whereas t_rel varied across conditions without systematic prolongation (0.59–1.09). These findings demonstrate that treatment mode strongly influences which growth phase is predominantly affected, highlighting the importance of phase-resolved kinetic analysis for distinguishing plasma-induced biological effects beyond conventional endpoint measurements. Full article

The application of Genome-Scale Metabolic Network Models (GSMM) in fermentation optimization is hampered by challenges in differentiating viable from dead cells and parameter distortion induced by conventional detection methods. Using E. coli BL21(DE3) as the model organism, this study developed a flux analysis strategy that couples cell kinetics with GSMM. Key parameters were estimated using the gradient descent algorithm, thereby enabling precise prediction of viable cell concentration and glucose consumption dynamics. Integrating this with the Quadratic Programming-based parsimonious Flux Balance Analysis (QP-pFBA) algorithm, intracellular metabolic reaction fluxes were quantified. Results demonstrated that the model can effectively differentiate viable from dead cells; Batch D, adopting the gradient-increasing feeding strategy, achieved the maximum specific growth rate (μ_max) of 0.6457, the highest among the four batches. Moreover, key metabolic reaction fluxes were highly correlated with the feeding strategy. This framework forgoes specialized, high-cost equipment and offers robust cross-strain/process adaptability, thereby greatly advancing GSMM utility. It provides a powerful tool for precise fermentation control and accelerates the shift toward data-driven biomanufacturing. Full article

In this study, the feasibility of electrospraying as an alternative processing technique for the preparation of composite solid rocket propellants (SRPs) was investigated. The main objective was to improve microstructural homogeneity and interfacial contact between the oxidizer, energetic additive, and metallic fuel without altering the chemical composition of the formulation. Additionally, porous electrosprayed SRP formulations were prepared to examine the influence of controlled porosity on thermal decomposition behavior. The prepared materials were characterized using scanning electron microscopy combined with energy-dispersive X-ray spectroscopy (SEM/EDS) to assess microstructural features and component distribution. Thermal decomposition behavior and kinetic parameters were evaluated using simultaneous DSC/TG analysis conducted at multiple heating rates. Safety-related properties were assessed through friction sensitivity testing, while post-decomposition solid residues were analyzed using SEM/EDS and X-ray diffraction. The results show that electrospraying improves structural homogeneity, reduces solid residue formation after thermal decomposition, and decreases apparent activation energy, while maintaining unchanged friction sensitivity. These findings demonstrate the potential of electrospraying as a physical processing route for tailoring the microstructure and thermal behavior of composite solid rocket propellants. Full article

Background: Snake envenomation represents a significant health concern in some regions of the world, with fatal cases occasionally requiring forensic investigation to estimate the postmortem interval (PMI). However, the influence of venom on carrion decomposition dynamics and arthropod succession patterns remains poorly understood, potentially compromising postmortem interval (PMI) estimations in such cases. Objectives: This study investigated the effects of Naja haje and Cerastes cerastes venoms on decomposition progression and necrophagous arthropod succession. Methods: Fifteen rabbits were allocated into three experimental groups. Two groups received median lethal intravenous doses (LD₅₀) of N. haje or C. cerastes venom, whereas the control group received a saline injection followed by CO₂ euthanasia. The carcasses were subsequently placed under natural field conditions and monitored daily for 15 days. Results: The presence of venom significantly altered decomposition dynamics. C. cerastes venom accelerated early decomposition, shortening both the fresh stage (1 ± 0.22 days vs. 2 ± 0.31 days in controls,) and bloating stage (3 ± 0.35 days vs. 5 ± 0.35 days), while extending both the decay stage (6 ± 0.3 days vs. 6 ± 0.17 days) and the dried stage (5.0 ± 0.44 days vs. 2 ± 0.039 days). N. haje venom showed intermediate effects. Overall arthropod abundance peaked on day 5 and declined thereafter. Control carcasses exhibited significantly higher arthropod abundance than carcasses envenomed with C. cerastes or N. haje. Conclusions: Snake envenomation significantly influenced decomposition kinetics and arthropod colonization patterns. Envenomation with C. cerastes venom produced more pronounced alterations than envenomation with N. haje venom. Full article

Sustainable agriculture is increasingly reliant on reducing anthropogenic inputs and recycling organic waste while protecting ecosystems. In this context, this study investigated the agro-environmental properties of biosulfate, focusing on its interaction with herbicides and its effects on soil fungi and horticultural plants. Two biosulfate samples obtained from urban sewage sludge from the Barletta (BIO-BA) and Foggia (BIO-FO) treatment plants were characterized by Fourier transform infrared–attenuated total reflectance (FTIR-ATR) spectroscopy and scanning electron microscopy (SEM). The adsorption/desorption of the herbicides metribuzin (MET), S-metolachlor (S-ME) and cycloxydim (CYC) on biosulfates was evaluated by studying adsorption kinetics and isotherms. All herbicides reached adsorption equilibrium within a few hours, according to pseudo-second-order kinetics, indicating a predominant chemical interaction between biosulfate and the molecules. Considering the organic C content of BIO-BA (~21%) and BIO-FO (~17%), which was less than half that commonly measured for other organic fertilizers, such as compost and digestate, their adsorption capacity was high, with Freundlich adsorption constants ranging from 772 µg g⁻¹ (S-ME on BIO-BA) to 1464 µg g⁻¹ (CYC on BIO-FO). A low hysteresis coefficient indicated a rather slow and incomplete release of the molecules from the biosulfate. Exposure of the fungi Pleurotus ostreatus and Pleurotus eryngii to 1, 2, 3, and 4% BIO-BA and BIO-FO stimulated mycelium growth, indicating that responses depended on fungal species and biosulfate dose. Finally, germination and early growth of lettuce and basil were generally unaffected by either biosulfate, as parameters such as germination percentage, root and shoot length, and fresh and dry biomass were not statistically different from the control. Some growth stimulation was observed in basil. Overall, biosulfate appears to be a promising soil fertilizer, as it can contribute to soil organic matter, retain xenobiotics, and exert biostimulatory effects under controlled conditions. Full article

As a primary reaction medium, water profoundly influences the kinetics and mechanisms of chemical processes. External physical treatments, such as vibration, can alter the physicochemical properties of water, thereby modifying reaction outcomes. This study aimed to investigate the effect of vibrational iterations (I0–I7) prepared using the “crossing” technology on the kinetics of the oxidation–reduction reaction between methylene blue and ascorbic acid, a standard model for evaluating external influences. Initial characterization revealed that while pH remained stable across all samples, electrical conductivity and dissolved oxygen levels deviated significantly from the control (intact water), with oxygen concentrations measuring either higher or lower than the control. Following the dissolution of methylene blue in these iterations, absorption spectroscopy was used to monitor decolorization kinetics. Different vibrational iterations influenced distinct kinetic parameters, including the rate constant, half-reaction time, and average reaction rate. Depending on the number of processing steps used to prepare the iterations, these parameters exhibited deviations ranging from 3% to 9% compared to the control. This suggests a complex relationship between the aqueous medium’s structural–dynamic properties and the reactants’ supramolecular organization. These findings underscore the potential of vibrational iterations as a tool for modulating chemical reaction kinetics through aqueous medium engineering. Further research is needed to elucidate the underlying mechanisms and expand the applicability of this approach to other systems. Full article

With ongoing development in the process industries, the accumulation of industrial inorganic solid wastes (IISWs) has become increasingly significant. IISWs are characterized by large volume and toxicity and pose challenges in treatment and control. IISWs from chemical processes mainly include red mud (RM), zinc slag, lithium slag (LS), electrolytic manganese residue (EMR), phosphogypsum (PG), water treatment sludge (WTS), sewage sludge, blast furnace slag (BFS), steel slag (SS), coal fly ash (CFA), coal gasification slag (CGS), copper smelting slag (CSS), and lead smelting slag (LSS). Having been chemically processed, they exhibit complex compositions that pose challenges for further utilization. In this paper, we comprehensively review the preparation of adsorbents from IISWs as raw materials, the applications of IISW-derived adsorbents, and their adsorption mechanisms. The obtained adsorbents include modified IISWs, zeolites, porous ceramics, and composite and hybrid adsorbents. The adsorption mechanisms, such as van der Waals forces, electrostatic interactions, and π–π interactions, contribute to the rapid adsorption kinetics and high adsorption capacity observed in these adsorbents. Full article

Over the years, poultry supply chains have prioritized highly productive genetic lines to meet consumer demand, often at the expense of meat quality, animal welfare, and animal health. Recently, however, industry trends have shifted toward a greater awareness of welfare, reduced farming intensity, and improved product quality. In response, the European Chicken Commitment (ECC) has advocated for the use of slower-growing genotypes, even within conventional production systems. This study aimed to evaluate the meat quality of two ECC-approved chicken genotypes with differing growth rates—slow-growing (SG: 30–40 g/day, Kabir) and medium-growing (MG: 40–50 g/day, Ranger Gold) in comparison with a fast-growing strain (FG: >65 g/day, Ross 308). A total of 300 chickens were assigned to two experimental conditions: a control group (C), with spontaneous activity, and a treatment group (M), subjected to induced moderate kinetic activity. The results demonstrated that genotype influenced the meat quality of chickens raised indoors more significantly than kinetic activity. Comparisons revealed that SG and MG chickens exhibited superior meat quality, particularly regarding protein content, oxidative status, and a more suitable fatty acid profile. Overall, our findings support the adoption of ECC-approved genotypes in indoor systems to simultaneously improve animal welfare and enhance the nutritional and technological quality of poultry meat. Full article

Background: Rift Valley fever virus (RVFV) is a significant mosquito-borne zoonotic virus with high public health and veterinary importance in Africa and the Middle East. Reliable diagnostic assays for detecting antibodies and assessing their functional neutralizing capacity are essential for surveillance programs, vaccine monitoring, and outbreak preparedness. Objective: This study evaluates and compares the analytical performance of a competitive enzyme-linked immunosorbent assay (cELISA) and a virus neutralization test (VNT) for detecting RVFV antibodies in vaccinated sheep sera, establishing an integrated laboratory workflow for virus titration, serological detection, and functional neutralization. Methods: Twenty serum samples were collected from sheep pre-vaccination and one month post-vaccination with Smithburn live attenuated RVFV vaccine. Sera were tested using a commercial multispecies RVFV competitive ELISA to detect antibodies specific to the viral nucleocapsid protein. Viral titration was conducted in Vero cells, and 50% tissue culture infective dose (TCID₅₀/0.1 mL) was calculated using the Reed and Muench method. VNT was performed at 24, 48, 72, and 96 h after infection with different viral doses (10² to 10⁵ TCID₅₀/0.1 mL), and the neutralizing ability of serial serum dilutions (1:2 to 1:1024) was tested. Compared with the control, protection was determined by cytopathic effect (CPE) inhibition. Results: ELISA revealed robust antibody signals up to a 1:32 dilution, with signal-to-noise (S/N) < 40%, whereas for higher dilutions, antibody detection became inconclusive or negative. Virus titration was performed to verify a stock concentration of 10^6.5 TCID₅₀/0.1 mL. The VNT exhibited time- and dose-dependent kinetics; high protection rates (≥97) were observed at 1:2–1:8 dilutions against 10²–10³ TCID₅₀/0.1 mL challenge doses; however, neutralizing efficacy decreased significantly at higher viral loads and higher serum dilutions. While cELISA and VNT results correlated strongly at low serum dilutions, the cELISA showed decreased sensitivity at dilutions ≥ 1:64, where the VNT remained capable of detecting functional neutralizing activity. Conclusions/Discussion: The results demonstrate that while both assays correlate well at high antibody concentrations, they diverge at lower concentrations. This discrepancy highlights the functional difference between binding antibodies (N-protein) and neutralizing antibodies (Gn/Gc glycoproteins). Consequently, the cELISA is ideal for rapid screening, whereas the VNT is indispensable for confirming functional immunity. Integrating both assays provides a more accurate immunological profile for RVFV surveillance and vaccine evaluation. Full article

Background/Objectives: In previous studies, chloroquine and ivermectin separately exhibited similar anticancer effects on various known cancer modulatory targets. This study aimed (1) to identify a non-toxic synergistic combination of chloroquine and ivermectin that suppresses hamster fibrosarcoma; (2) to verify combined antitumor efficacy using dose–response analysis; and (3) to investigate potential synergistic mechanisms by restoring tumor progression with the reciprocal cancer-modulating agent deoxycholic acid. Methods: A BHK-21/C13 cell culture was subcutaneously inoculated into Syrian golden hamsters randomly divided into groups (6 animals per group): (1) untreated control; treated daily (17 days after inoculation) with (2) chloroquine 50 mg/kg; (3) ivermectin 5 mg/kg; (4) a combination of chloroquine 50 mg/kg and ivermectin 5 mg/kg; (5) a combination of chloroquine 50 mg/kg, ivermectin 5 mg/kg and deoxycholic acid 100 mg/kg; (6) a combination of chloroquine 25 mg/kg and ivermectin 2.5 mg/kg; (7) a combination of chloroquine 12.5 mg/kg and ivermectin 1.25 mg/kg. Dose–response curves were generated for chloroquine and ivermectin combinations. Characteristics of tumors (growth kinetics, biophysical, histological, immunohistochemical, pathological), hamster organs, biochemical and hematological blood tests were compared among the groups. Results: The synergistic, dose-dependent anticancer effects of two antiparasitic agents, similar tumor-regulation modulators chloroquine and ivermectin, in doses equivalent to human doses were observed in fibrosarcoma in hamsters (both drugs approximately 1/10 LD₅₀) without toxicity and in various cell lines of human lung, colon and cervical carcinomas and hamster fibrosarcoma in vitro. The addition of a reciprocal modulator of cancer regulation, NF-κB stimulator deoxycholic acid, caused a huge rescue effect on fibrosarcoma and a reversal of the successful anticancer therapy using the combination. Conclusions: The chloroquine and ivermectin combination may be recommended for comprehensive additional preclinical and clinical evaluation due to its synergistic anticancer effects. Further preclinical and clinical exploration will be crucial to thoroughly define the optimal role of the combination therapy in the treatment of fibrosarcoma and potentially other cancer types. Full article

This review examines biodegradable polymer-based core–shell nanoformulations encapsulating essential oils for acne treatment through the lens of physicochemical design and controlled delivery mechanisms. Acne is a common inflammatory skin disorder closely associated with sebum overproduction and microbial imbalance, while conventional therapies, although effective, may present long-term side effects. Increasing attention has therefore turned to sustainable dermatological materials derived from eco-friendly polymers combined with naturally active compounds. Recent advances show that core–shell nanostructures fabricated from biodegradable polymers function as physicochemically engineered carriers for volatile essential oils. They enhance their stability and protect them from premature degradation. They also enable controlled release governed by diffusion, polymer relaxation, interfacial interactions, and degradation kinetics. This review highlights how polymer chemistry, interfacial properties, particle morphology, and processing routes determine encapsulation efficiency, release profiles, and skin permeation behaviour. Particular emphasis is placed on structure–property–function relationships, including mass transport phenomena, thermodynamic compatibility between polymers and essential oils, surface charge, wettability, and nanostructure architecture, which collectively influence bioavailability and therapeutic performance. By integrating concepts from polymer physical chemistry, colloid and interface science, and drug delivery kinetics, these sustainable nanoformulations emerge as promising platforms for acne and sebum control. Overall, essential oil-loaded biodegradable polymeric core–shell systems represent a sustainable and scientifically grounded approach to acne management, although further physicochemical characterization, in vivo validation, and consideration of cost, technical challenges, and current limitations are required to support clinical translation. Full article

Ultrafine hematite particles (<10 μm), commonly generated in beneficiation circuits, exhibit poor flocculation and slow settling, posing challenges for solid–liquid separation. This study investigates the influence of the anionic polyacrylamide (APAM) molecular weight on ultrafine hematite flocculation under controlled laboratory conditions, combining macroscopic experiments with molecular dynamics simulations (MDSs). Sedimentation tests show that the APAM molecular weight strongly affects settling kinetics, supernatant clarity, and floc structure, with the settling rate, flocculation-stage reaction time, supernatant turbidity, and underflow concentration exhibiting a non-monotonic trend and optimal performance at seven million. Under this condition, particles aggregate most efficiently, achieving a turbidity of 182 NTU, an underflow concentration of 51.5%, and the largest compact flocs, averaging 379.8 μm with a fractal dimension of 1.71. Higher molecular weights (≥9 million) induce chain coiling, reduce floc compactness, increase water retention, and impair settling. MDS indicates that polymer–surface interactions improve with an increasing polymerisation degree only up to an intermediate chain length; a polymerisation degree of 30 exhibits the most favourable extended–flexible conformation, maximal surface enrichment, strongest coordination between carboxyl groups and surface Fe atoms, lowest adsorption energy, and fastest adsorption kinetics. The functional-group distribution and hydrogen-bond analyses show that –NH₂ and –COO^– groups dominate interfacial interactions, with a polymerisation degree of 30 yielding the highest density of interfacial hydrogen bonds. By correlating macroscopic experiments with molecular-scale observations, this work provides mechanistic insight into how the APAM chain length governs ultrafine hematite flocculation, highlighting the role of polymer conformation and multipoint adsorption in controlling the settling performance. Full article