Search Results (344)

Background/Objectives: Mesoporous silica materials, particularly KIT-6, offer promising features, such as large surface area, tunable pore structures, and biocompatibility, making them ideal candidates for advanced drug delivery systems. The aims of this study were to develop and evaluate an innovative modified-release platform for metformin hydrochloride (MTF), using KIT-6 mesoporous silica as a matrix, to enhance oral antidiabetic therapy. Methods: KIT-6 was synthesized using an ultrasound-assisted sol-gel method and subsequently loaded with MTF via adsorption from alkaline aqueous solutions at two concentrations (1 and 3 mg/mL). The structural and morphological characteristics of the matrices—before and after drug loading—were assessed using SEM-EDX, TEM, and nitrogen adsorption–desorption isotherms (the BET method). In vitro drug release profiles were recorded in simulated gastric and intestinal fluids over 12 h. Kinetic modeling was performed using seven classical models, and a multifractal theoretical framework was used to further interpret the complex release behavior. Results: The loading efficiency increased with increasing drug concentration but nonlinearly, reaching 56.43 mg/g for 1 mg/mL and 131.69 mg/g for 3 mg/mL. BET analysis confirmed significant reductions in the surface area and pore volume upon MTF incorporation. In vitro dissolution showed a biphasic release: a fast initial phase in an acidic medium followed by sustained release at a neutral pH. The Korsmeyer–Peppas and Weibull models best described the release profiles, indicating a predominantly diffusion-controlled mechanism. The multifractal model supported the experimental findings, capturing nonlinear dynamics, memory effects, and soliton-like transport behavior across resolution scales. Conclusions: The study confirms the potential of KIT-6 as a reliable and efficient carrier for the modified oral delivery of metformin. The combination of experimental and multifractal modeling provides a deeper understanding of drug release mechanisms in mesoporous systems and offers a predictive tool for future drug delivery design. This integrated approach can be extended to other active pharmaceutical ingredients with complex release requirements. Full article

This study aimed to characterize and evaluate the fibrinolytic, thrombolytic, hematological, and toxicological aspects of a serine protease (AsKSP) from Aspergillus tamarii Kita UCP 1279. The enzyme was purified using a two-phase aqueous system and assessed for optimal pH (7.0) and temperature (50 °C), stability, and effects of metal ions, inhibitors, and surfactants. AsKSP exhibited stability for up to 120 min at 50 °C and 36 h at pH 7.0. Enzymatic activity was enhanced by Na⁺ and Zn²⁺ and non-ionic surfactants (Tween-80) but inhibited by Cu²⁺, Fe³⁺, Triton X-100, and SDS, reducing activity by up to 62.35%. The highest amidolytic activity was observed for the substrate N-succinyl-Gly–Gly–Phe-p-nitroanilide. SDS-PAGE analysis indicated an approximate molecular mass of 90 kDa. The enzyme showed fibrinolytic activity, degrading 38.81% of fibrin clots in vitro after 90 min, without affecting fibrinogen. Cytotoxicity assays indicated no toxicity (cell viability > 80%). Coagulation assays showed slight prolongation of prothrombin time (PT) and activated partial thromboplastin time (aPTT), with no effect on thrombin time. No red blood cell lysis was observed, and albumin increased enzymatic activity by 31.70%. These findings demonstrate that Aspergillus tamarii Kita UCP 1279 produces a fibrinolytic protease with potential for thrombus treatment, providing a promising foundation for drug development. Full article

The Bundelkhand granite (BG) constitutes the bulk of the granitoid complex in the Bundelkhand Craton and preserves imprints of its evolution from the magmatic to a protracted hydrothermal stage as deduced from the petrography. In order to reconstruct such a path of evolution in this study, thermobarometric calculations were attempted on the mineral chemistry of the major (hornblende, plagioclase, biotite) and minor (epidote, apatite) magmatic phases. They yielded magmatic temperatures and pressures (in excess of 700 °C and ~5 kbar), although not consistently, and indicate mid-crustal conditions at the onset of crystallization. Temperatures in the hydrothermal regime within the BG are better constrained by the chemistry of the chlorite and epidote minerals (340 to 160 °C) that conform with the ranges of homogenization temperatures of aqueous–biphase inclusions in matrix quartz in the BG and subordinate quartz veins. These reconstructions indicate that fluid within the BG evolved down to lower temperatures and towards the deposition of quartz and, more importantly, bears a striking similarity to the temperature–salinity characteristics of fluid in the giant quartz reef system. Scanty mixed aqueous–carbonic inclusions in the BG are indicative of the CO₂-poor nature of the BG magma and the exsolution of CO₂ at lower pressure (~2.6 kbar). The dominant mechanism of fluid evolution in the BG appears to be the incursion of meteoric fluid, which caused fluid dilution. Laser Raman microspectrometry reveals many types of solid phases in aqueous–carbonic inclusions in the BG domain. The occurrence of unusual, effervescent-type inclusions, though infrequent, bears a striking similarity to that reported in the giant quartz reef domain. Thus, the highlight of the present work is the convincing fluid inclusion evidence that genetically links the BG with the giant quartz reef system, although many cited discrepancies arise from the radiometric dates. We visualize the episodic release of silica-transporting fluid to the major fracture system (now occupied by the giant reef) from the BG, thus making the fluid in the two domains virtually indistinguishable. Full article

This study investigates pegmatites with exceptionally rare mineralogical and chemical signatures, hosted by the 1.8 Ga peralkaline albite-enriched granite, which corresponds to the renowned Madeira Sn-Nb-Ta-F (REE, Th, U) deposit in Pitinga, Brazil. Four distinct pegmatite types are identified: border pegmatites, pegmatitic albite-enriched granite, miarolitic pegmatite, and pegmatite veins. The host rock itself has served as the source for the fluids that gave rise to all these pegmatites. Their mineral assemblages mirror the rare-metal-rich paragenesis of the host rock, including pyrochlore, cassiterite, riebeckite, polylithionite, zircon, thorite, xenotime, gagarinite-(Y), genthelvite, and cryolite. These pegmatites formed at the same crustal level as the host granite and record a progressive magmatic–hydrothermal evolution driven by various physicochemical processes, including tectonic decompressing, extreme fractionation, melt–melt immiscibility, and internal fluid exsolution. Border pegmatites crystallized early from a F-poor, K-Ca-Sr-Zr-Y-HREE-rich fluid exsolved during solidification of the pluton’s border and were emplaced in contraction fractures between the pluton and country rocks. Continued crystallization toward the pluton’s core produced a highly fractionated melt enriched in Sn, Nb, Ta, Rb, HREE, U, Th, and other HFSE, forming pegmatitic albite-enriched granite within centimetric fractures. A subsequent pressure quench—likely induced by reverse faulting—triggered the separation of a supercritical melt, further enriched in rare metals, which migrated into fractures and cavities to form amphibole-rich pegmatite veins and miarolitic pegmatites. A key process in this evolution was melt–melt immiscibility, which led to the partitioning of alkalis between two phases: a K-F-rich aluminosilicate melt (low in H₂O), enriched in Y, Li, Be, and Zn; and a Na-F-rich aqueous melt (low in SiO₂). These immiscible melts crystallized polylithionite-rich and cryolite-rich pegmatite veins, respectively. The magmatic–hydrothermal transition occurred independently in each pegmatite body upon H₂O saturation, with the hydrothermal fluid composition controlled by the local degree of melt fractionation. These highly F-rich exsolved fluids caused intense autometasomatic alteration and secondary mineralization. The exceptional F content (up to 35 wt.% F in pegmatite veins), played a central role in concentrating strategic and critical metals such as Nb, Ta, REEs (notably HREE), Li, and Be. These findings establish the Madeira system as a reference for rare-metal magmatic–hydrothermal evolution in peralkaline granites. Full article

The Cuyu gold deposit in central Jilin Province in Northeast China is located in the eastern segment of the northern margin of the North China Craton (NCC), as well as the eastern segment of the Xing’an–Mongolian Orogenic Belt (XMOB). Gold ore-bodies are controlled by NW-trending faults and mainly occur in late Hercynian granodiorite. The mineralization process in the Cuyu deposit can be divided into three stages: quartz + coarse grained arsenopyrite + pyrite (stage I), quartz + sericite + pyrite + arsenopyrite + electrum + chalcopyrite + sphalerite (stage II), and quartz + calcite ± pyrite (stage III). Stage II is the most important for gold mineralization. We conducted analyses including petrography, microthermometry, laser Raman spectroscopy of fluid inclusions, and H–O–S–Pb isotopic analysis to elucidate the mineralization processes in the Cuyu deposit. Five types of primary fluid inclusions (FIs) are present in the hydrothermal quartz and calcite grains of the ore: liquid-rich two-phase aqueous fluid inclusions (L-type), vapor-rich two-phase aqueous fluid inclusions (V-type), CO₂-bearing two- or three-phase inclusions (C1-type), CO₂-rich two- or three-phase inclusions (C2-type), and pure CO₂ mono-phase inclusions (C3-type). From stages I to III, the fluid inclusion assemblages changed from L-, C2-, and C3-types to L-, V-, C1-, C2-, and C3-types and, finally, to L-types only. The corresponding homogenization temperatures for stages I to III were 242–326 °C, 202–298 °C, and 106–188 °C, and the salinities were 4.69–9.73, 1.63–7.30, and 1.39–3.53 wt.% NaCl equiv., respectively. The ore-forming fluid system evolved from a NaCl-H₂O-CO₂ ± CH₄ ± H₂S fluid system in stage I and II with immiscible characteristics to a homogeneous NaC-H₂O fluid system in stage III. Microthermometric data for stages I to III show a decreasing trend in homogenization temperatures and salinities. The mineral assemblages, fluid inclusions, and H–O–S–Pb isotopes indicate that the initial ore-forming fluids of stage I were exsolved from diorite porphyrite and characterized by a high temperature and low salinity. The addition of meteoric water in large quantities led to decreases in temperature and pressure, resulting in a NaCl-H₂O-CO₂ ± CH₄ ± H₂S fluid system with significant immiscibility in stage II, facilitating the deposition of gold and associated polymetallic sulfides. The Cuyu gold deposit has a similar ore genesis to those of gold deposits in the Jiapigou–Haigou gold belt (JHGB) of southeastern Jilin Province indicating potential for gold prospecting in the northwest-trending seam of the JHGB. Full article

The effects of a series of sodium salts (Na₃PO₄, Na₂CO₃, Na₂SO₄, Na₂SO₃, Na₂MO₄, Na₂CrO₄, and Na₂WO₄) on the phase separation of poly(ethylene glycol) (PEG) solutions in water at PEG concentrations of 0.5 to 30 wt.% were studied. The salts’ effects on phase separation are found to correlate with the change in the entropy related to the structural changes in water during anion hydration. The same salts’ effects on phase separation in aqueous solutions of branched PEG and polyvinylpyrrolidone at a polymer concentration of 10 wt.% were also examined. The results obtained support the assumption that phase separation in aqueous polymer–salt systems is an entropy-driven process. Full article

The complex interaction of hydrothermal fluids and carbonate rocks is recognized to promote significant impacts on petroleum systems, reservoir porosity, and potential. The objective of this study is to investigate the fluid phases entrapped in the mineral phases of the Barra Velha Formation (Santos Basin), including their petrographic paragenetic relationships, relative timing, temperatures of migration events, and maximum temperature reached by the sedimentary section. The petrographic descriptions (387), Rock-Eval pyrolysis (107), fluid inclusion petrography (14), and microthermometry (428) were performed on core and sidewall samples from two wells from one field of the Santos Basin. Hydrocarbon source intervals were primarily identified in lithologies with high argillaceous content. Chert samples still retain some organic remnants indicative of their original composition prior to extensive silicification. Redeposited intraclastic rocks exhibit the lowest organic content and oil potential. A hydrothermal petroleum system is identified by fluids consisting in gas condensate, light to heavy undersaturated oil, occasionally accompanied by aqueous fluids influenced by juvenile and evaporitic sources, and localized flash vaporization events. These hydrothermal fluids promoted silicification and dolomitization, intense brecciation, and lead to enhanced porosity in different compartments of the reservoir. The relative ordering of paleo-hydrothermal oils and the main oil migration and accumulation events has improved our understanding of the petroleum systems in the basin. This contribution is significant for future regional research on the evolution of fluid systems and their implications for carbonate reservoirs. Full article

Natural pigments like betacyanins are highly unstable under heat, light, acid, and alkaline conditions. Yeast protein (YP) is a promising substitute protein, while chitooligosaccharides (COS) are water-soluble alkaline polysaccharides. Water-in-oil-in-water (W₁/O/W₂) emulsions, with two-membrane, three-phase structure, can serve as effective carriers for stabilizing pigments. In this study, YP-COS complexes formed through electrostatic interactions were used as hydrophilic emulsifiers to create betacyanin-coated W₁/O/W₂ emulsions. The W₁/O colostrum was designed to make up 30%, 70%, and 90% of the emulsion (v/v)and the W₂ was designed by the complexes with three concentrations of YP (2%, 1.25% and 0.5%, w/v)-COS (6%, 3.75% and 1.5%, w/v). The optimal formulation was determined through comprehensive evaluation of micromorphological characteristics, particle size, zeta potential and creaming index, ultimately yielding a system comprising YP (2%)-COS (6%) and 90% W₁/O colostrum. Moreover, the W₁/O/W₂ emulsion system significantly improved the betacyanins retention under thermal treatment, photolytic exposure, pH gradients, and extended storage compared to the betacyanin aqueous solution (p < 0.05). In vitro digestion tests showed the emulsion retained 58.39% of betacyanins, while the betacyanin aqueous solution retained only 41.42%, demonstrating the emulsion’s ability to delay the betacyanins release, offering new insights for using YP-COS complexes in food production and other fields. Full article

The blueberry fruit (Vaccinium corymbosum L.) exhibits a high content of bioactive compounds, including anthocyanins, that can be used as pigmenting agents, but they are mixed with sugars, which can hinder their utilization. The objective was to evaluate the use of aqueous two-phase extraction aided by centrifugation to separate bioactive compounds, particularly anthocyanins, from blueberry fruits, considering the reduction of sugars, for their use as pigmenting agents in a food product. A mixture of trisodium citrate (Na₃C₃H₅O(COO)₃; Na₃Cit) and polyethylene glycol ([HO-(CH₂CH₂O)n-CH₂OH]; poly (ethane-1,2-diol); PEG) with a molecular weight of 4 kDa was used. Based on the cloud point method, a binodal diagram was developed. After the evaluation of several systems with composition located on a tie line, conditions were identified to form biphasic systems with phases of equal volume. Passive sedimentation for 0, 15, and 30 min, followed by centrifugation and also passive sedimentation for 24 h without centrifugation, were evaluated. A system with 17.73% Na₃Cit, 21.33% PEG, 30 min of passive sedimentation, and 15 min of centrifugation at 2940× g produced an extract with a high concentration of soluble phenols (0.353 mg/mL) and anthocyanins (0.202 mg/mL) and, likewise, high antioxidant activity (910.0 mmol gallic acid equivalents per mL), with reduced sugar content, which demonstrated to have the potential to pigment food beverages with a reddish tone. Full article

Food waste remains a critical global concern, with approximately one third of all food produced being ultimately discarded. Therefore, it is urgent to develop new techniques for the effective repurpose of waste. Aqueous two-phase systems (ATPSs) stand out as a simple and biocompatible liquid–liquid extraction technique for the recovery of bioactive substances from food waste. In ATPSs, the target species partition between two liquid phases, according to affinity, which facilitates its extraction. This work aimed at extracting three polyphenols—chlorogenic acid (CA), ferulic acid (FA), and resveratrol (RV)—through the application of eco-friendly ATPSs composed of water, ethyl lactate (EL), and organic salts, namely disodium succinate (Na₂Succinate) and disodium tartrate (Na₂Tartrate), for future application in the valorisation of food waste. All partitions presented successful results, with values of partition coefficients (K) higher than 1 and extraction efficiencies (E) higher than 50%, indicating a preferential migration of the polyphenols to the top phase. The extraction of FA using the ATPS based on Na₂Tartrate presented the most promising results, with K = 19 ± 6 and E = (94.2 ± 0.9)% for the longest tie-line. Additionally, a comparison with previous works of the research group was drawn, with the extraction of RV exhibiting outstanding performance across all studied ATPSs. Therefore, the assessed ATPSs were shown to hold immense potential for the recovery of polyphenols. Full article

The development of heterostructures incorporating photocatalysts optimized for visible-light activity represents a major breakthrough in the field of environmental remediation research, offering innovative and sustainable solutions for environmental purification. This study explores the photocatalytic capabilities of a SnFe₂O₄/g-C₃N₄ heterojunction nanocomposite, successfully synthesized from graphitic carbon nitride (g-C₃N₄) and tin ferrate (SnFe₂O₄) and applied to the degradation of the cationic dye brilliant cresyl blue (BCB) in an aqueous solution. These two components are particularly attractive due to their low cost and ease of fabrication. Various characterization techniques, including XRD, FTIR, SEM, and TEM, were used to confirm the successful integration of SnFe₂O₄ and g-C₃N₄ phases in the synthesized catalysts. The photocatalytic and photo-Fenton-like activity of the heterojunction composites was evaluated by the degradation of brilliant cresyl blue under visible LED illumination. Compared to the pure components SnFe₂O₄ and g-C₃N₄, the SnFe₂O₄/g-C₃N₄ nanocomposite demonstrated a superior photocatalytic performance. Furthermore, the photo-Fenton-like performance of the composites is much higher than the photocatalytic performances. The significant improvement in photo-Fenton activity is attributed to the synergistic effect between SnFe₂O₄ and g-C₃N₄, as well as the efficient separation of photoexcited electron/hole pairs. The recyclability of the SnFe₂O₄/g-C₃N₄ composite toward BCB photo-Fenton like degradation was also shown. This study aimed to assess the modeling and optimization of photo-Fenton-like removal BCB using the SnFe₂O₄/g-C₃N₄ nanomaterial. The main parameters (photocatalyst dose, initial dye concentration, H₂O₂ volume, and reaction time) affecting this system were modeled by two approaches: a response surface methodology (RSM) based on a Box–Behnken design and artificial neural network (ANN). A comparison was made between the predictive accuracy of RSM for brilliant cresyl blue (BCB) removal and that of the artificial neural network (ANN) approach. Both methodologies provided satisfactory and comparable predictions, achieving R² values of 0.97 for RSM and 0.99 for ANN. Full article

This study proposes an innovative two-step synthesis strategy to significantly enhance the performance of sodium-ion batteries by developing low-defect, low water content iron-based Prussian blue (PB) materials. Addressing the limitations of traditional co-precipitation methods—such as rapid reaction rates leading to excessive crystal defects and interstitial water content—the research team introduced a synergistic approach combining non-aqueous phase precursor synthesis and controlled water-concentration secondary crystallization. The process involves preparing a PB precursor in a glycerol system, followed by secondary crystallization in a water-/ethanol-mixed solvent with a precisely regulated water content, achieving the dual objectives of water content reduction and crystal morphology optimization. Systematic characterization revealed that water concentration during secondary synthesis critically influences the material’s crystal structure, morphological features, and water content. The optimized PB50-24 material exhibited a highly regular cubic morphology with a sodium content of 9.2% and a remarkably low interstitial water content of 2.1%. Electrochemical tests demonstrated outstanding performance—an initial charge–discharge capacity of 120 mAh g⁻¹ at a 1C rate, the retention of 105 mAh g⁻¹ after 100 cycles, and a high rate capability of 86 mAh g⁻¹ at 10C, representing significant improvements in cycling stability and rate performance over conventional methods. This work not only establishes a cost-effective, scalable synthesis pathway for Prussian blue materials but also provides theoretical guidance for developing other metal-based Prussian blue analogs, offering substantial value for advancing the industrial application of sodium-ion batteries in next-generation energy storage systems. Full article

Microencapsulation using a double emulsion system can improve the viability of probiotic cells during storage and digestion. In this study, a double emulsion system W_C/O/W_F was designed to microencapsulate Lactobacillus rhamnosus GG using pea protein (PP) and cellulose nanocrystals (CNCs) at various proportions, and the effect of their proportions on the stability and efficacy of the encapsulation system was studied. The double emulsions were prepared by a two-step emulsification process: the internal aqueous phase containing probiotic strain (W_C) was homogenized into the oil phase (O), which was then homogenized into the external aqueous phase (W_F) containing 15% wall materials with varying proportions of PP and CNCs [F1 (100:0), F2 (96:4), F3 (92:8), F4 (88:12), F5 (84:16), F6 (80:20)]. The incorporation of CNCs significantly lowered the average particle size and improved the stability of the emulsions. The encapsulation efficiency did not differ significantly across the tested formulations (63–68%). To check the effectiveness of the designed system, a simulated digestion study was conducted in two phases: gastric phase and intestinal phase. The double emulsion microencapsulation significantly improved the viability of encapsulated cells during digestion compared against free cells. Microscopic analysis along with assessment of protein hydrolysis of the double emulsions during the simulated digestion demonstrated a two-stage protection mechanism. This study presented promising results for employing a double emulsion system for the microencapsulation of probiotics and the potential of PP and CNCs in designing such systems. Full article

This systematic study was conducted on the separation of yttrium (Y) and erbium (Er) from a chloride medium using a mixed extractant system composed of [N1444][P507] and TRPO (trialkylphosphine oxide) in kerosene. This investigation focused on the effects of various extractants, extraction systems, the initial acidity of the aqueous phase, and the phase contact time on the extraction efficiencies of Y and Er. This study showed that using the combination of [N1444][P507] and TRPO notably increased the extraction performance and enhanced the separation factor between Y and Er, outperforming the individual use of P507 or [N1444][P507] under identical conditions. The extraction efficiencies for Y and Er reached 88.4% and 93.3%, respectively, with a separation factor (Er/Y) of 1.84, highlighting the system’s effectiveness in selectively isolating rare earth elements. Optimal stripping conditions were obtained using 0.1 mol/L of HCl, resulting in a successful recovery of 93.1% of Y³⁺ and 78.9% of Er³⁺ from the organic phase. The extraction mechanism involved both ion exchange and ion association. The enthalpy changes (ΔH) associated with the extraction of Y³⁺ (−2.5 kJ·mol⁻¹) and Er³⁺ (4.6 KJ·mol⁻¹) demonstrate that the extraction processes are exothermic, reflecting the thermodynamic differences between the two ions. Full article

This work presents an imaging testing system (software and hardware) that can generate repeatable images through a stabilized port in the soil for processes known to change with time. The system includes (i) a stabilized port in the ground made of standard PVC pipe, with sections lined with a borosilicate glass tube, and (ii) a digital imaging instrument to survey the optically transparent portion of the stabilized port. The instrument uses a probe containing a digital camera and two light sources, one using white lights and one using ultraviolet (UV) lights (365 nm). The main instrument controls the probe using a cable within the stabilized port to take overlapping pictures of the soil under the different light sources. Two examples are provided, one to document the distribution of soil and groundwater contaminants known as non-aqueous phase liquids (NAPL, which include petroleum) at variable water saturation levels and a second one to monitor the growth of a plant over a 2-week interval. In both examples, the system successfully identified critical changes in soil processes and showed a resolution of approximately 15 µm (in the order of the thickness of a human hair), demonstrating the potential for repeated imaging of soil processes known to experience temporal changes. Both examples are illustrative, as additional applications might be possible. The novelty of this system lies in its ability to generate repeated measurements at larger depths than the current shallow systems installed by hand. Full article