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22 pages, 2116 KB  
Article
Optimizing Self-Emulsifying Drug Delivery Systems for the Oral Delivery of a Hydrophobic Ion-Paired Lysozyme Complex
by Martin Deák, Nur Aslan, Eslam Ramadan, Katalin Kristó, Gábor Katona and Tamás Sovány
Pharmaceutics 2026, 18(2), 275; https://doi.org/10.3390/pharmaceutics18020275 - 23 Feb 2026
Abstract
Background: The oral delivery of biopharmaceuticals remains a major challenge for researchers and the pharmaceutical industry. Therefore, extensive research is ongoing to develop a viable delivery method, hence self-emulsifying drug delivery systems (SEDDSs) are being investigated because of their ability to protect [...] Read more.
Background: The oral delivery of biopharmaceuticals remains a major challenge for researchers and the pharmaceutical industry. Therefore, extensive research is ongoing to develop a viable delivery method, hence self-emulsifying drug delivery systems (SEDDSs) are being investigated because of their ability to protect the carried macromolecules in the gastrointestinal environment and facilitate absorption through the intestinal barrier. Objectives: To systematically investigate this promising method for the oral delivery of lysozyme (LYZ) and to model oral peptide/protein administration. Methods: LYZ/sodium dodecyl sulfate (SDS) hydrophobic ion pairs (HIPs) were prepared to enhance protein solubility and stability in SEDDSs. Different surfactants (Tween® 20 and 80) and as co-surfactants (Span® 20 and 80) were combined for the preparation of liquid SEDDSs according to a 22 full factorial design and samples of each combination were formulated based on a three-factor-constrained mixture design. The critical quality attributes (CQAs), droplet size, polydispersity index (PDI), and zeta potential were measured by dynamic light scattering (DLS). The process design space was determined by response surface methodology (RSM) and two-dimensional ternary contour plots. An in vitro release test was performed using the sample-and-separate approach. Results: Emulsions of SEDDSs with the optimal properties of droplet size < 200 nm, PDI < 0.4 and zeta potential < −10 mV were prepared. Consequently, a HIP load of 10 mg/g was achievable, exhibiting apparent first-order kinetics, with approximately 80% of the loaded LYZ released within 6 h. Conclusions: This study may contribute to better understanding of the effects and interactions of formulating materials for SEDDSs and their possible role in the oral delivery of biopharmaceuticals. Full article
(This article belongs to the Section Drug Delivery and Controlled Release)
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25 pages, 653 KB  
Article
Effect of Packaging Method (Under Vacuum vs. Air) on Quality and Shelf Life of Carp (Cyprinus caprio) Fish Balls Stored at Fridge for 14 Days
by Agnieszka Kaliniak-Dziura, Marek Kowalczyk, Monika Ziomek, Piotr Skałecki, Piotr Domaradzki, Ewa Poleszak, Jarosław Szponar and Mariusz Florek
Molecules 2026, 31(4), 746; https://doi.org/10.3390/molecules31040746 (registering DOI) - 22 Feb 2026
Abstract
The study aimed to assess the influence of two packaging methods (under vacuum, VP vs. air, AP) on the quality of fish balls from carp (Cyprinus carpio) stored at +4 °C up to 14 days after preparation. The air-packed and vacuum-packed [...] Read more.
The study aimed to assess the influence of two packaging methods (under vacuum, VP vs. air, AP) on the quality of fish balls from carp (Cyprinus carpio) stored at +4 °C up to 14 days after preparation. The air-packed and vacuum-packed fish balls were analyzed for physicochemical parameters, microbiological status, and sensory characteristics. The packaging method and storage time interaction significantly (p < 0.05) affected the acid value (AV) and peroxide value (PV), as well as the thiobarbituric acid reactive substance index (TBARS), with lower values of these parameters observed in vacuum-packed samples at 7 d (AV, PV, TBARS), 9 d (TBARS), 12 d (PV) and 14 d (TBARS) of storage. Moreover, vacuum packaging helped maintain a beneficial oil absorption and pH, and partially slowed down the occurrence of undesirable changes in color, i.e., the decrease in redness of semi-raw fish balls or increase in yellowness of deep-fried products. Based on the overall quality values, the air-packed fish balls were sensory acceptable for up to 9 days, while the vacuum-packed fish balls were acceptable up to 12 d. The bacterial counts (total viable counts—TVC, psychrotrophic bacterial counts—PBC, total staphylococcal counts—TSC, sulfite-producing bacteria counts—SPBC, and lactic acid bacteria counts—LABC) increased during storage. Although the rate and pattern of growth varied depending on the packaging, fish balls maintained the recommended microbiological quality throughout the entire storage period. The VP method inhibited the growth of TVC, PBC, TSC, and SPBC relative to the AP method, while the VP method showed a higher increase in LABC. The results indicated that vacuum packaging appears to be an effective approach to prolong the shelf life of fish balls made from carp. Additionally, developing this convenient food product could be a valuable strategy to enhance consumer acceptance and promote the use of widely farmed carp species. Full article
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23 pages, 4942 KB  
Article
A Laboratory Investigation on Utilization of Alkali-Activated By-Products in Deep Soil Mixing in Silty Sands
by Önder Akçakal and Mustafa Hatipoğlu
Sustainability 2026, 18(4), 2138; https://doi.org/10.3390/su18042138 - 22 Feb 2026
Abstract
Cement is one of the primary construction materials in ground improvement applications that employ the binder stabilization method. Due to the high carbon dioxide emissions in its production, evaluating environmentally friendly alternative binder materials is a popular research topic. Industrial by-products such as [...] Read more.
Cement is one of the primary construction materials in ground improvement applications that employ the binder stabilization method. Due to the high carbon dioxide emissions in its production, evaluating environmentally friendly alternative binder materials is a popular research topic. Industrial by-products such as fly ash (FA) and ground granulated blast-furnace slag (GGBS) are alternatives to traditional cement, especially in deep soil mixing (DSM) applications, and can enhance sustainability in construction projects. Since these materials are not active when used alone, alkali activation is proposed to modify them as binding agents in ground improvement projects. This study presents the outcomes of a primary laboratory test phase for on-site applications. FA and GGBS precursors supplied by local plants, mixed with soil and activator solutions in applicable ratios, and samples were prepared for laboratory tests. Unconfined compression tests were applied with strain measurements after several curing durations, between 1 and 54 weeks. Average compression strength and modulus of elasticity values were recorded at approximately 12.3 MPa and 11.7 GPa, respectively, in samples with an average dosage. An empirical correlation between the strength and stiffness modulus was found. Strength and stiffness values were comparable to traditional materials, indicating the potential of these industrial by-products when activated under alkali conditions. The carbon footprints of cement and alkali-activated by-products were compared based on calculated CO2-eq emissions. Full article
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18 pages, 2414 KB  
Article
Co-Ce PROX Catalysts for Renewable, Climate-Independent, and Emission-Free “On-Board” Energy
by Silviya Zh. Todorova, Bozhidar K. Grahovski, Elena Maria Anghel, Daniela B. Karashanova, Zlatka Geshkova, Hristo Kolev, Diana Filkova, Krasimir Tenchev, Iliyana Hristova and Vesselin Idakiev
Processes 2026, 14(4), 711; https://doi.org/10.3390/pr14040711 (registering DOI) - 21 Feb 2026
Viewed by 150
Abstract
Trace amounts of CO in H2-rich gas can poison Pt electrodes in proton-exchange-membrane fuel cells, necessitating selective CO removal. Preferential oxidation of CO (PROX) offers an efficient route to oxidize CO while preserving H2. Although noble-metal-based catalysts are widely [...] Read more.
Trace amounts of CO in H2-rich gas can poison Pt electrodes in proton-exchange-membrane fuel cells, necessitating selective CO removal. Preferential oxidation of CO (PROX) offers an efficient route to oxidize CO while preserving H2. Although noble-metal-based catalysts are widely used, their high cost has driven interest in non-precious alternatives. Co3O4–CeO2 catalysts have emerged as particularly promising due to their high activity and stability. Two series of Co–Ce/SiO2 catalysts were prepared via impregnation: in the first, Ce was introduced and calcined prior to Co deposition; in the second, Co and Ce nitrates were co-deposited from a mixed aqueous solution. The latter method enhances the interaction between Co3O4 and CeO2, increasing the availability of surface oxygen species. Stability tests on the most active sample demonstrated remarkable durability, maintaining near-complete CO conversion over 100 h on dry stream. Full article
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25 pages, 4351 KB  
Article
Mechanistic Insights into AAV Capsid–Stationary Phase Interactions Governing Native Stability and Chromatographic Separation Using AAV8 as a Model System
by Timotej Žvanut, Mitja Martelanc, Aleš Štrancar and Andreja Gramc Livk
Pharmaceutics 2026, 18(2), 263; https://doi.org/10.3390/pharmaceutics18020263 - 20 Feb 2026
Viewed by 120
Abstract
Background/Objectives: Adeno-associated viruses (AAVs) are widely used gene therapy vectors; yet their physicochemical stability and chromatographic behavior are highly sensitive to the solution conditions they are in. Effective separation of full (F), empty (E), and partially filled (P) capsids—most commonly achieved by anion [...] Read more.
Background/Objectives: Adeno-associated viruses (AAVs) are widely used gene therapy vectors; yet their physicochemical stability and chromatographic behavior are highly sensitive to the solution conditions they are in. Effective separation of full (F), empty (E), and partially filled (P) capsids—most commonly achieved by anion exchange (AEX) chromatography—is essential for standard analytical characterization, process development, and product safety. However, conventional AEX methods rely on low-conductivity alkaline mobile phases with low salt, which promote capsid binding and therefore higher resolution, at the expense of structural stability. Conversely, formulations such as near-neutral buffers might preserve capsid integrity but often impair AEX retention and separation resolution. Methods: Here, we extend a mechanistic investigation using AAV8 capsids as a model system, focusing on detailed capsid interactions with strong AEX, and present novel AAV8 separation strategies on a weak AEX stationary phase. Results: By systematically varying buffer pH and ionic strength, we identify operational regimes that balance capsid stability with chromatographic separation efficiency. In parallel, we introduce an integrated two-dimensional (2D) in-line buffer exchange configuration that decouples AEX performance from sample formulation, enabling robust separation of stability-optimized, high-salt matrices without off-line desalting. Conclusions: By elucidating the roles of capsid charge modulation, ligand physicochemical properties, and local microenvironmental buffering, this study establishes practical design principles for stability-preserving chromatography. It lays a foundation for more reliable analytical and future preparative AAV workflows. Full article
(This article belongs to the Special Issue Adeno-Associated Virus (AAV) as a Vector for Gene Therapy)
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22 pages, 1098 KB  
Article
Integrated Microfluidic Chip Enabling Preparation and Immobilization of Cell-Laden Microspheres, and Microsphere-Based Cell Culture and Analysis
by Qiongyao Mou, Peiyi Zhang, Daijing Li, Qiong Wang and Jun Yang
Biosensors 2026, 16(2), 126; https://doi.org/10.3390/bios16020126 - 19 Feb 2026
Viewed by 86
Abstract
Microfluidics-based preparation methods for cell-laden hydrogel microspheres are well-suited for large-scale comparative analysis of single or few cells. However, in existing studies, the preparation of cell-laden hydrogel microspheres and the cell culture process are typically separated, requiring the fabricated microspheres to be eluted [...] Read more.
Microfluidics-based preparation methods for cell-laden hydrogel microspheres are well-suited for large-scale comparative analysis of single or few cells. However, in existing studies, the preparation of cell-laden hydrogel microspheres and the cell culture process are typically separated, requiring the fabricated microspheres to be eluted and transferred from the preparation device to cell culture dishes or plates for cultivation. This transfer process can easily compromise sterility, while conventional cell culture methods consume more reagents and cause microsphere stacking, hindering single-cell observation and analysis. To address these issues, this paper presents an integrated microfluidic chip that sequentially enables droplet generation with cell encapsulation, gel droplet solidification, hydrogel microsphere trapping, and microsphere-based cell culture and analysis, facilitating the cultivation and observation of single or small numbers of cells. Integrating cell-laden microsphere preparation and 3D cell culture within a sealed chip structure reduces contamination risks associated with cell transfer, enables automation of multiple cell analysis workflows, and minimizes reagent and sample consumption. Using polydimethylsiloxane (PDMS) with good gas permeability and processability as the chip material, biocompatible fluorinated oil was selected as the oil phase for microsphere preparation. A mild sodium alginate-calcium ion gelation system was employed, where calcium ions were released under acidic conditions after droplet generation to trigger solidification, yielding uniform hydrogel microspheres. Under optimized conditions, the single-cell encapsulation efficiency for test samples of human myeloid leukemia cells (K562) was 33.8% ± 1.8%, with a size uniformity coefficient of variation (CV) reaching 3.85%. Cells encapsulated within hydrogel microspheres were cultured in 286 on-chip independent cell culture chambers, achieving >95% viability after 24 h. Full article
17 pages, 3512 KB  
Article
Promoting Recycling Efficiency Through the Use of Sub-Terahertz Waves for Proper Wood Identification
by Dai Otsuka, Yui Miyazaki, Mizue Kato, Hitoshi Hamasaki, Jeongsoo Yu, Xiaoyue Liu and Tadao Tanabe
Sustainability 2026, 18(4), 2088; https://doi.org/10.3390/su18042088 - 19 Feb 2026
Viewed by 142
Abstract
Past studies have reported that carbon dioxide emissions during combustion vary depending on the tree species used as fuel. It has also been reported that the moisture content of wood affects combustion efficiency. From this perspective, identifying the tree species and moisture content [...] Read more.
Past studies have reported that carbon dioxide emissions during combustion vary depending on the tree species used as fuel. It has also been reported that the moisture content of wood affects combustion efficiency. From this perspective, identifying the tree species and moisture content is crucial for utilizing waste wood as a resource. Therefore, this study verified the effectiveness of non-destructive diagnosis using terahertz waves. Samples with adjusted moisture content were prepared for eight types of wood. Each wood sample was irradiated with multiple broadband terahertz electromagnetic waves, and their transmission characteristics were compared. Experimental results revealed a strong negative correlation (Pearson Correlation coefficient: −0.98~−0.71 square meter/gram) between the sample’s specific gravity and transmittance when irradiated with 65 GHz and 90 GHz sub-terahertz waves. This trend was particularly pronounced during 90 GHz sub-terahertz irradiation. Furthermore, it was found that the trend in transmittance variation differed depending on the wood’s moisture content. These results indicate that terahertz waves are effective as a wood identification method capable of distinguishing between coniferous and broadleaf trees. Furthermore, they are considered effective for predicting wood moisture content. This research is expected to contribute to promoting wood recycling and the sustainable use of wood resources. Full article
(This article belongs to the Section Environmental Sustainability and Applications)
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12 pages, 561 KB  
Article
Development and Evaluation of a Lyophilized Plasma-Based Internal Quality Control for Human Immunodeficiency Virus Rapid Diagnostic Tests
by Siriphailin Jomjunyoung, Wanvisa Treebuphachatsakul, Supaporn Suparak, Nam K. Tran, Gerald J. Kost and Napaporn Apiratmateekul
Diagnostics 2026, 16(4), 608; https://doi.org/10.3390/diagnostics16040608 - 19 Feb 2026
Viewed by 128
Abstract
Background/Objectives: Rapid diagnostic tests (RDTs) for human immunodeficiency virus (HIV) are widely used, but most kits lack standardized internal quality control (IQC) materials. In this study, we aimed to develop and evaluate a plasma-based IQC compatible with five HIV RDT brands and with [...] Read more.
Background/Objectives: Rapid diagnostic tests (RDTs) for human immunodeficiency virus (HIV) are widely used, but most kits lack standardized internal quality control (IQC) materials. In this study, we aimed to develop and evaluate a plasma-based IQC compatible with five HIV RDT brands and with proven long-term stability. Methods: Control samples at three reactivity levels were tested with five HIV RDT kits in lyophilized and liquid forms. Lyophilized samples were produced with and without trehalose, whereas liquid samples were prepared with and without StabilZyme™ SELECT Stabilizer (Stabilizer). Accelerated stability testing was performed at 37 °C and 45 °C for 28 days, and the most stable formulation was selected for long-term storage at 4 ± 2 °C and 25 ± 5 °C. Stability was assessed based on test-line visibility and signal intensity. Signal-intensity trends were analyzed using simple linear regression with a t-test on the slope; samples were considered stable when no significant trend was detected (p > 0.05). Results: Reactivity measured using the Elecsys HIV combi PT assay yielded cutoff index (COI) values of 772.65 (1:8) for the strong-positive control and 269.95 (1:25) for the weak-positive control. Trehalose-containing lyophilized samples maintained reactivity under accelerated testing at 37 and 45 °C and for 6 months at 4 ± 2 °C and 25 ± 5 °C, with no significant change in signal intensity (p > 0.05). Conclusions: The plasma-based IQC materials were compatible with all five HIV RDTs, and trehalose-stabilized lyophilized plasma showed high stability, supporting transport and storage without strict cold-chain requirements. Full article
(This article belongs to the Special Issue Point-of-Care Testing (POCT) for Infectious Diseases)
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19 pages, 3282 KB  
Article
Rapid Detection of Black Pepper Adulteration with Endogenous and Exogenous Materials: Assessment of Benchtop and Handheld Infrared Spectrometers
by Paul Rentz, Alina Mihailova, Horacio Heinzen, Martine Bergaentzlé, Elisa Ruhland, Marivil D. Islam, Islam Hamed, Christina Vlachou, Simon Kelly, Said Ennahar and Dalal Werner
Foods 2026, 15(4), 754; https://doi.org/10.3390/foods15040754 - 19 Feb 2026
Viewed by 125
Abstract
Black pepper is the most widely used spice crop globally and has significant economic value, making it a target for economically motivated adulteration. A wide range of organic and inorganic bulking materials has been used as adulterants in black pepper. Development of rapid [...] Read more.
Black pepper is the most widely used spice crop globally and has significant economic value, making it a target for economically motivated adulteration. A wide range of organic and inorganic bulking materials has been used as adulterants in black pepper. Development of rapid non-targeted screening methods for use at different stages of the black pepper supply chain is extremely important for the identification and prevention of evolving fraudulent practices. This study has assessed the potential of benchtop Fourier Transform infrared with attenuated total reflectance (FTIR-ATR), benchtop Fourier Transform near-infrared (FT-NIR), and two handheld NIR spectrometers, coupled with chemometrics, for the discrimination of black pepper (Piper nigrum), pepper from other species and genera (non-Piper nigrum) and a broad range (n = 27) of endogenous and exogenous adulterants. Spiked samples were prepared to imitate pepper adulteration with seven different adulterants at five levels of adulteration (5%, 25%, 50%, 75%, 95% w/w). Orthogonal partial least squares discriminant analysis (OPLS-DA) achieved 100% total prediction accuracy for both FTIR-ATR and FT-NIR in differentiating authentic Piper nigrum and adulterant samples. The handheld microNIR 1700ES resulted in a 91.30% correct classification rate, while the SCiO model achieved 86.96% prediction accuracy. Detection of black pepper adulteration with multiple adulterants was performed using data-driven soft independent modelling of class analogy (DD-SIMCA). The highest performance of the DD-SIMCA model was achieved by FTIR-ATR (100% sensitivity and 100% specificity) followed by FT-NIR (98% sensitivity and 99% specificity). The handheld microNIR 1700ES resulted in 95% sensitivity and 90% specificity. This study demonstrated that FTIR-ATR and FT-NIR, coupled with DD-SIMCA, can effectively detect black pepper adulteration with multiple endogenous and exogenous adulterants. The handheld NIR (microNIR1700ES) clearly demonstrated the potential for rapid and effective verification of Piper nigrum authenticity outside the laboratory. Full article
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20 pages, 1962 KB  
Article
Optimizing Lysis and Extraction Workflows for Enrichment-Free qPCR Detection of Salmonella enterica in Poultry Matrices
by Rejoice Nyarku, Emmanuel Kuufire, Kingsley E. Bentum, Viona Osei, Asmaa Elrefaey, Tyric James, Yilkal Woube, Evangelyn Alocilja, Temesgen Samuel and Woubit Abebe
Pathogens 2026, 15(2), 229; https://doi.org/10.3390/pathogens15020229 - 18 Feb 2026
Viewed by 172
Abstract
Salmonella remains a leading cause of foodborne illness worldwide, with poultry products representing a major source of human exposure, underscoring the need for rapid and reliable detection methods. Although qPCR offers sensitive and timely pathogen detection, assay performance is highly dependent on sample [...] Read more.
Salmonella remains a leading cause of foodborne illness worldwide, with poultry products representing a major source of human exposure, underscoring the need for rapid and reliable detection methods. Although qPCR offers sensitive and timely pathogen detection, assay performance is highly dependent on sample preparation efficiency and nucleic acid purity, particularly in complex food matrices. In this study, we systematically optimized the sample preparation workflow of a SYBR Green based qPCR assay for enrichment-free detection of Salmonella enterica in poultry. Multiple lysis chemistries, incubation times, DNA extraction methods, centrifugation strategies, inoculum sources, and magnetic nanoparticle (MNP) assisted workflows were evaluated using phosphate-buffered saline and chicken rinsate matrices. Among the conditions tested, lysis with 20 µL Proteinase K and 400 µL PrepMan™ for 20 min produced the lowest and most consistent Cq values. Although Promega Wizard® produced slightly lower mean Cq values than PrepMan™, statistical analysis showed no significant differences between extraction methods or centrifugation protocols, indicating comparable overall performance. Broth-derived inocula yielded earlier and more reproducible Cq values than colony-derived preparations. In contrast, inclusion of MNP processing resulted in higher Cq values in both matrices compared to the non-MNP workflow. Overall, these findings demonstrate that optimized lysis, extraction, and centrifugation workflows enhances the consistency and analytical reliability of direct qPCR detection of Salmonella in poultry matrices, supporting laboratory-based rapid detection applications. Full article
(This article belongs to the Section Bacterial Pathogens)
15 pages, 1121 KB  
Article
Detection and Quantification of Corn Starch and Wheat Flour as Adulterants in Milk Powder by Raman Spectroscopy Coupled with Chemometric Routines
by Edwin R. Caballero-Agosto, Louang D. Cruz-Dorta, Samuel P. Hernandez-Rivera, Leonardo C. Pacheco-Londoño and Ricardo Infante-Castillo
Sensors 2026, 26(4), 1304; https://doi.org/10.3390/s26041304 - 18 Feb 2026
Viewed by 108
Abstract
Adulteration of milk powder (MP) is performed, especially in underdeveloped countries, by adding corn starch (CS) or wheat flour (WF) without mentioning it. Multiple techniques have been established to reduce these deceptive methods. Most of these techniques require samples to be sent to [...] Read more.
Adulteration of milk powder (MP) is performed, especially in underdeveloped countries, by adding corn starch (CS) or wheat flour (WF) without mentioning it. Multiple techniques have been established to reduce these deceptive methods. Most of these techniques require samples to be sent to the laboratory for results through a time-consuming, expert-requiring, and destructive procedure. Raman spectroscopy (RS) has seen application due to the availability of portable modalities and its non-destructive, water-insensitive nature. Using principal component analysis (PCA), the differences and similarities between MP and the adulterants (CS and WF) have been evaluated. To quantify the percentages of CS and WF binary mixtures independently with MP, partial least squares regression (PLSR) has been employed. A total of 70 MP samples independently adulterated with CS and WF were prepared. Thirteen chemometric modes were developed by combining the first and second derivatives with Standard Normal Variate (SNV) and Multiplicative Scatter Correction (MSC) to quantify adulteration. The results obtained for CS and WF mixtures show errors of 0.76 and 0.77 %w/w, respectively, with the optimized math pretreatment. These results demonstrate that the portable RS modality can be used as an effective technique for detecting adulterants in milk powder. Full article
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31 pages, 11360 KB  
Article
Optical Dilatometry and Push-Rod Dilatometry—A Case Study for Sintering Steel and Zirconia Tapes
by Daniel Gruner, Tim Gestrich, Mathias Herrmann, Anne Günther, Jan Mahling, Chao Liu, Christoph Broeckmann and Alexander Michaelis
J. Exp. Theor. Anal. 2026, 4(1), 10; https://doi.org/10.3390/jeta4010010 - 17 Feb 2026
Viewed by 120
Abstract
In this work, the sintering behavior of tapes prepared via tape casting from stainless-steel and zirconia powders is investigated by optical—as well as push-rod—dilatometry. Both methods are compared in terms of sample preparation, measurement conditions, and advantages and disadvantages. The experimental work shows [...] Read more.
In this work, the sintering behavior of tapes prepared via tape casting from stainless-steel and zirconia powders is investigated by optical—as well as push-rod—dilatometry. Both methods are compared in terms of sample preparation, measurement conditions, and advantages and disadvantages. The experimental work shows the advantages of optical dilatometry in the characterization of the sintering behavior of load-free sintering tapes and the possibility of simultaneously observing sample warpage and deformation. Push-rod dilatometry requires a constant load on the sample, which influences measurement in the case of tapes with lower mechanical stability due to their sensitivity to deformation, but it has advantages because of its higher accuracy in measuring dimensional changes. In the case of warpage, shrinkage due to the sintering of the sample is superimposed by an irregular deformation process that can be separated by analytical methods. No in-plane shrinkage anisotropy of the tapes is observed for either type of tape. In the case of the push-rod dilatometer, an additional peak in the shrinkage rate is observed in the early stage of compaction, along with a slight shift and an increased maximum in the compaction rate. This is most likely due to the effects of the contact pressure of the push-rod. Full article
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26 pages, 1923 KB  
Article
Study of Composite Photocatalysts Obtained by Photodeposition of Platinum on Layered Oxide HCa2Nb3O10 and Its Inorganic–Organic Hybrids
by Nikita A. Davydov, Oleg I. Silyukov, Ivan A. Rodionov, Sergei A. Kurnosenko, Alexandra N. Gubanova, Alina V. Kulagina and Irina A. Zvereva
Molecules 2026, 31(4), 685; https://doi.org/10.3390/molecules31040685 - 16 Feb 2026
Viewed by 180
Abstract
In recent decades, layered perovskite-like oxides have been intensively investigated as prominent photocatalysts for water splitting as a method of hydrogen production. In many previous papers, it was shown that deposition of platinum on an oxide sample dramatically increases photocatalytic activity. Nevertheless, little [...] Read more.
In recent decades, layered perovskite-like oxides have been intensively investigated as prominent photocatalysts for water splitting as a method of hydrogen production. In many previous papers, it was shown that deposition of platinum on an oxide sample dramatically increases photocatalytic activity. Nevertheless, little research was conducted to reveal the localisation of platinum in layered oxides; either it is located on the surface or in the interlayer space. In the present work, an attempt to answer this question is made. An HCa2Nb3O10 layered perovskite-like oxide was modified with platinum by photoreduction of H2PtCl6 and then was intercalated with n-alkylamines (R = Me, Bu, Oc). Moreover, another set of samples were prepared by intercalating the amines first into HCa2Nb3O10, followed by Pt deposition. Besides conventional methods for sample characterisation, we measured the kinetics of Pt dissolution during aqua regia etching of the samples, hoping that the rate of platinum dissolution would provide some information about its localisation. It was shown that in HCa2Nb3O10 modified with platinum, less than 20% of the platinum is located on the surface, and that in the case of HCa2Nb3O10 intercalated with amines, an even smaller amount of platinum attaches to the surface. Moreover, Pt in HCa2Nb3O10 intercalated with amines was found to be significantly more stable against aqua regia treatment than in HCa2Nb3O10 decorated with platinum directly. Full article
23 pages, 2377 KB  
Article
Phytochemical Screening and Physicochemical Properties of Oil Extract of Usnea barbata L. F.H.Wigg from Călimani Mountains, Romania
by Mihaela Afrodita Dan, Oana Cioancă, Violeta Popovici, Adina Magdalena Musuc, George Mihai Nițulescu, Mihai Anastasescu, Emma Adriana Ozon, Ioana Cristina Marinas, Claudia Maria Guțu, Daniela Luiza Baconi, Denisa Ioana Udeanu, Monica Hăncianu, Adrian Florin Șpac, Andreea Roxana Ungureanu and Dumitru Lupuliasa
Int. J. Mol. Sci. 2026, 27(4), 1903; https://doi.org/10.3390/ijms27041903 - 16 Feb 2026
Viewed by 275
Abstract
Green cosmetics are primarily based on plant-derived ingredients and use sustainable biotechnological tools for their preparation. The present research aimed to investigate the Usnea barbata (U. barbata) extract in Jojoba oil (JO) enriched with 5% Peppermint oil (PEO) and 10% Vitamin [...] Read more.
Green cosmetics are primarily based on plant-derived ingredients and use sustainable biotechnological tools for their preparation. The present research aimed to investigate the Usnea barbata (U. barbata) extract in Jojoba oil (JO) enriched with 5% Peppermint oil (PEO) and 10% Vitamin E, as a potential natural product for skin applications. The U. barbata oil extract (UBPJO) was obtained through cold maceration. Phytochemical screening was performed using Gas Chromatography/Mass Spectrometry (GC-MS), Folin–Ciocalteu method, and Graphite-Furnace Atomic Absorption Spectrophotometry (GFAAS). Fourier Transform Infrared Spectroscopy (FTIR) and Atomic Force Microscopy (AFM) were used to evaluate the physicochemical properties. Then, rheological characteristics and oxidation stability (measured as the time to reach the oxidation starting point, induction period (IP)) of both oil samples (UBPJO and oil mixture alone (PJO) were investigated. Total phenolic content (TPC) in UBPJO was 2.5 times higher than in PJO (p < 0.05), while heavy metal levels (As and Pb) were slightly higher (p > 0.05). UBPJO has higher shear stress, viscosity, and spreadability than PJO, but the differences are not significant (p > 0.05). Finally, IP measurements indicated appreciable oxidative stability (UBPJO vs. PJO: 153.02 h vs. 137.35 h, p > 0.05). The phytochemical composition and physicochemical properties support the inclusion of UBPJO in various skincare formulations. Full article
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Article
Thermo-Responsive Hydroxypropyl Methylcellulose and Sodium Alginate Composite Hydrogels and Their Fire Extinguishing Properties
by Xiaodong Pei, Jiahui Chen, Huafeng Liu, Liang Wang, Zhendong Miao, Yujie Yuan, Jialin Xi, Chenglin Li, Chenhao Tian and Yanzhao Liu
Fire 2026, 9(2), 88; https://doi.org/10.3390/fire9020088 - 16 Feb 2026
Viewed by 271
Abstract
To effectively prevent and control coal spontaneous combustion, a novel heat-sensitive hydrogel for mine fire prevention and extinguishment was developed using hydroxypropyl methylcellulose (HPMC) and the organic flame-retardant, sodium alginate (SA). The hydrogel was prepared through single-factor variable control and material compounding. First, [...] Read more.
To effectively prevent and control coal spontaneous combustion, a novel heat-sensitive hydrogel for mine fire prevention and extinguishment was developed using hydroxypropyl methylcellulose (HPMC) and the organic flame-retardant, sodium alginate (SA). The hydrogel was prepared through single-factor variable control and material compounding. First, the optimal formulation of the hydrogel was determined using analytical instruments and techniques, including a viscometer, vacuum drying oven, and the inverted test tube method. Subsequently, its microstructural characteristics were examined using scanning electron microscopy (SEM) and infrared spectroscopy (FTIR). Finally, a fire suppression test platform was established to perform comparative experiments, verifying the hydrogel’s fire prevention, extinguishing, and cooling performance. Experimental results demonstrated that the optimal hydrogel formulation consists of 2.5 wt% HPMC and 0.3 wt% SA. At this ratio, the hydrogel exhibits excellent fluidity and water retention, ensuring prolonged coverage and wetting of coal surfaces. The gel undergoes a sol–gel phase transition at 58 °C, enabling it to fill voids, bind and reinforce coal particles, and reduce exposed surface area. After drying, the hydrogel forms a uniformly smooth surface capable of both coating the coal body and encapsulating individual coal particles. Following the hydrogel treatment, the coal sample retains its original functional groups, indicating that no chemical reactions occur during mixing. Compared with traditional inhibitors, the hydrogel demonstrates superior fire suppression performance, more effectively covering and encapsulating burning coal. It rapidly reduces the temperature to 28 °C by the cooling effect of water evaporation from the hydrogel, and it maintains thermal stability, achieving outstanding fire-extinguishing efficiency. Full article
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