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Quercetin is a flavonoid that occurs in many types of fruit and vegetables and is stable for no longer than 4.5 h in the investigated pH range (6.0-8.0), even at 4 °C in the dark. At higher temperatures, the degradation/oxidation process is much faster. Simple but effective proliposomal encapsulation was used to protect the quercetin from environmental conditions such as pH. With this approach, 65 to 90% of pure quercetin and quercetin-rich onion extract was kept after >60 days under conditions that favoured its oxidation (pH 7.4). In addition, the encapsulated quercetin decreases the lipid peroxidation induced by pulsed UV light by >50%. At a mass ratio of 1:100 quercetin to lipids (w/w), the liposomes remained intact in solutions for six months. Quercetin in lipid bilayers simultaneously protects the unsaturated lipids from peroxidation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

Understanding the stability of NPs in different aqueous environments, related with their size is crucial for assessing their potential risks. This is influenced by several factors, including pH, ionic strength, and the presence of biomolecules, or dissolved organic matter (DOM). In this study, dispersions of NPs derived from common plastic waste materials, including polystyrene (PS), polyethylene terephthalate (PET), polyvinyl chloride (PVC), polymethyl methacrylate (PMMA), and polycarbonate (PC), were synthesized by a nanoprecipitation method with sizes: 189 ± 7, 58 ± 3, 123 ± 4, 151 ± 7 and 182 ± 6 nm, respectively. Stability for a period of 14 days of these NPs was assessed in various natural water matrices. Different analytical techniques were used, including Asymmetric Flow Field-Flow Fractionation (AF4) coupled with UV-Vis and Dynamic Light Scattering (DLS) in series, batch DLS, Fourier-Transform Infrared Spectroscopy-Attenuated Total Reflection (FTIR-ATR), and Transmission Electron Microscopy (TEM). None of the studied NPs was stable in seawater and NPs were transformed in microplastics (MPs) by aggregation. PET was more prone to aggregation in all waters and PS was the most stable followed for PC, PVC and PMMA. However, bottle and tap waters maintained better the original size of NPs. For the most stable dispersion PS, the influence of heteroaggregation in tap and lagoon waters and aging from exposure to UV light in sea water were tested. In both cases, the stability over time was worse for PS. The results can contribute to a more comprehensive understanding of the fate and behaviour of NPs in natural aquatic environments, emphasizing the importance of studying a wide range of polymers., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)

Air-processed perovskite solar cells are desirable for the large-scale manufacturing application in the future, yet the presence of moisture and oxygen goes against perovskite crystallization and deteriorates phase stabilization, leading to the formation of substantial defective nano-impurities, especially on the vulnerable surface. Here, we propose a strategy to simultaneously remove superficial defect layer and solidify the surface by soaking air-fabricated perovskite film into low-polar organic esters at elevated temperature to trigger an in-situ dynamic surface lattice disassemble and reconstruction process. Molecular dynamics simulations and experimental results indicate that the inorganic CsPbI2Br perovskite is first dissolved and then the Br-rich phase is recrystallized at solid-liquid interface owing to the balance between weak solubility and high-temperature induced annealing process, thus hardening the soft surface and releasing the lattice tensile stress, which benefits the minimization of interfacial recombination and improvement of the structural stability. As a result, we prepare a carbon-based CsPbI2Br device in complete air without precise control on humidity, achieving a champion efficiency of 15.37% with excellent resistance to harsh attackers. This method offers a promising avenue for overcoming the limit of processing conditions on advancing perovskite-based optoelectronic devices., (© 2024 Wiley‐VCH GmbH.)

The mass production of graphene oxide (GO) has garnered significant attention in recent years due to its potential applications in various fields, from materials science to biomedicine. Graphene, known for its unique properties, such as high conductivity and mechanical strength, has been extensively studied. However, traditional production methods such as the exfoliation of graphite with scotch tape are not suitable for large-scale production. This has led to an increased focus on GO as a viable alternative to graphene production. Nonetheless, challenges, including the optimization of oxidation processes, the control of structural uniformity, and the reproducibility of production, have not been solved so far. This review critically examines GO production advancements by analyzing experimental and mechanistic studies to identify significant developments that enable high-yield and reproducible methods suitable for industrial-scale production. Special attention is given to oxidation techniques and postsynthesis purification and storage, with a focus on controlled oxidation to achieve homogeneous and single-layer GO. Through this lens, the review outlines the path forward for the industrialization of GO, aiming to bridge the gap between academic research and industrial production.

Background: Primary aromatic amines (PAAs) present significant challenges in the prediction of mutagenicity using current standard quantitative structure activity relationship (QSAR) systems, which are knowledge-based and statistics-based, because of their low positive prediction values (PPVs). Previous studies have suggested that PAAs are metabolized into genotoxic nitrenium ions. Moreover, ddE, a relative-energy based index derived from quantum chemistry calculations that measures the stability nitrenium ions, has been correlated with mutagenicity. This study aims to further examine the ability of the ddE-based approach in improving QSAR mutagenicity predictions for PAAs and to develop a refined method to decrease false positive predictions., Results: Information on 1,177 PAAs was collected, of which 420 were from public databases and 757 were from in-house databases across 16 laboratories. The total dataset included 465 Ames test-positive and 712 test-negative chemicals. For internal PAAs, detailed Ames test data were scrutinized and final decisions were made using common evaluation criteria. In this study, ddE calculations were performed using a convenient and consistent protocol. An optimal ddE cutoff value of -5 kcal/mol, combined with a molecular weight ≤ 500 and ortho substitution groups yielded well-balanced prediction scores: sensitivity of 72.0%, specificity of 75.9%, PPV of 65.6%, negative predictive value of 80.9% and a balanced accuracy of 74.0%. The PPV of the ddE-based approach was greatly reduced by the presence of two ortho substituent groups of ethyl or larger, as because almost all of them were negative in the Ames test regardless of their ddE values, probably due to steric hindrance affecting interactions between the PAA and metabolic enzymes. The great majority of the PAAs whose molecular weights were greater than 500 were also negative in Ames test, despite ddE predictions indicating positive mutagenicity., Conclusions: This study proposes a refined approach to enhance the accuracy of QSAR mutagenicity predictions for PAAs by minimizing false positives. This integrative approach incorporating molecular weight, ortho substitution patterns, and ddE values, substantially can provide a more reliable basis for evaluating the genotoxic potential of PAAs., Competing Interests: Declarations. Ethics approval and consent to participate: Not applicable. Consent for publication: Not applicable. Competing interests: The authors declare that there are no competing interests., (© 2024. The Author(s).)

Faba bean is an important legume crop with significant potential to contribute to sustainable agricultural systems and food security in Ethiopia. Despite its importance, the crop is prone to various biotic and abiotic constraints that can reduce seed yield and affect its stability and adaptability. To identify stable and adaptable genotypes, 10 faba bean genotypes were evaluated at three locations over two growing seasons using different stability parameters. Genotype-by-environment interaction (GGE biplot) and additive main effect and multiplicative interaction (AMMI) analyses are the statistical methods used to evaluate crop genotype performance across different environments to identify high-performing, stable, and adaptable genotypes and to highlight preferable environments for genotype differentiation. This study utilized cultivar superiority, regression coefficients, and deviations from regression parameters that provide valuable insights into genotype performance under varying environmental conditions. This approach helps to identify robust cultivars that can thrive across different agricultural settings and challenges, ultimately contributing to improved crop production and food security. The results revealed that G9, G8, and G7 are the three most stable and adaptable genotypes. These faba bean genotypes showed greater resilience to environmental changes and improved suitability for sustainable production, making them better options for local farmers. They also bolster resilience against climate variability and ultimately ensure agricultural sustainability. The AMMI model indicated that the genotype-environment interaction (GEI) significantly influences seed yield. These findings provide crucial insights into the genetic potential of faba bean genotypes that can help breeding programs to develop high-yielding, adaptable, and stable varieties for the region and other areas with similar agro-ecological conditions., Competing Interests: Declarations. Ethics approval and consent to participate: Not applicable. Competing interests: The authors declare no competing interests., (© 2024. The Author(s).)

Inverted perovskite solar cells (PSCs) have captured significant interest due to their outstanding stability, cost-effective fabrication process, and good compatibility with flexible and tandem devices. The presence of bulk and surface defects is key factor in PSCs that cause non-radiative recombination and degradation. To improve the efficiency and stability of inverted PSCs, a bulk-to-surface dual-passivation strategy is employed by utilizing Oleylamine Iodide (OAmI) as additives and 4-Fluorobenzylamine Hydroiodide (4-F-PMAI) as surface passivating agents. Utilizing OAmI as bulk passivation can enhance the crystallinity of perovskite films and reduce lattice defects. Meanwhile, 4-F-PMAI further suppresses non-radiative recombination and reduces open-circuit voltage (V OC ) loss through bidentate anchoring. Consequently, the dual-passivation strategy significantly enhances device performance, boosting the power conversion efficiency (PCE) of PSCs to 24.26%, with a V OC of 1.15V. Moreover, the unencapsulated PSCs show excellent long-term stability maintaining over 85% and 90% of the initial efficiency under 85 °C thermal annealing in N 2 for 1000 hours and after storage in ambient conditions (RH: 30 ± 5%) for 1000 hours., (© 2024 Wiley‐VCH GmbH.)

The electrochemical degradation of Pt/C in commercial proton exchange membrane fuel cells (PEMFCs) is a major challenge that limits their durability and performance. This degradation mainly arises from carbon corrosion, which facilitates the detachment of electrocatalyst particles that are weakly bound to catalyst supports. Herein, unusually robust hollow gyroid morphologies designed for strong electrocatalyst fixation and extensive surface accessibility during oxygen reduction reactions (ORR) are reported. To obtain self-assembled gyroid nanostructures using a poly(styrene-b-2-vinylpyridine) (PS-b-P2VP) block copolymer, a solvent vapour treatment with dimethylformamide, which is highly selective for the P2VP block, is applied. It is discovered that retaining residual solvent in the gyroid-forming P2VP microdomain before carbonization is crucial for forming hollow gyroids with embedded electrocatalysts. These hollow gyroid carbon-Pt (HGC-Pt) nanostructures exhibit a 3.6-fold enhancement in electrochemically active surface area compared to solid gyroid carbon (SGC) counterparts. Based on systematic analyses, this exceptional electrochemical stability is attributed to greatly enhanced surface accessibility derived from the hollow geometry, uniform and robust catalyst embedding, and extensive pyridinic nitrogen doping from the P2VP block., (© 2024 The Author(s). Advanced Materials published by Wiley‐VCH GmbH.)

Modulating self-aggregation and charge transport in the upper acceptor layer of the pseudo planar heterojunction (PPHJ) is crucial for enhancing dielectric constant and suppressing trap density, leading to efficient and stable organic photovoltaics (OPVs). In this work, a metal complex acceptor (MCA), PtAC-Cl, is selectively incorporated into the upper host Y6 layer of PPHJ to regulate morphology and fill trap states. There exists a strong chemical interaction between PtAC-Cl and Y6, which can promote electron transfer. PtAC-Cl can regulate the self-aggregation and extend the exciton diffusion length of Y6, resulting in enhanced charge transport and reduced energetic disorder. Consequently, upper layer-modulated PPHJ devices with PtAC-Cl achieved a significant power conversion efficiency of 18.16%. The universality of PtAC-Cl is also demonstrated in PM6/eC9 and PM6/L8-BO systems, achieving the highest PCEs of 18.79 and 19.30%, respectively. All the improved PCEs are mainly attributed to the enhanced fill factor (FF) and short circuit current (J sc ) compared with the controls. Additionally, PtAC-Cl significantly improves the thermal stability and photostability of the devices, with a T 80 lifetime of ≈ 401 h under continuous illumination with simulated 1-Sun light and 1265 h under continuous heating at 70 °C. Overall, this work introduces the concept of MCA and proposes a practical and efficient method to enhance the efficiency and stability of OPVs through selective upper-layer modulation in PPHJ with MCA., (© 2024 Wiley‐VCH GmbH.)

Polysaccharide-protein complexes have proven to be effective nano-carrier with high stability. In this work, walnut protein hydrolysates (WPH) prepared through limited enzymolysis were considered as encapsulation carriers to solve the limited water solubility and bioavailability of icariin, a bioactive compound in functional foods. The pH-driven method was employed to prepare WPH-icariin nanoparticles (WPHI). Their characterization, formation, digestive properties, and immunomodulatory activity were investigated. The results showed that WPHI possessed superior encapsulation efficiency (82.35 %) and loading capacity (137.2 μg/mg) for icariin. Its water solubility (1647 μg/mL) and bioavailability (94.86 %) were significantly improved, by over 80 and 30 times, respectively. The combination of WPH with icariin resulted in the formation of irregular lamellar structure through hydrophobic, electrostatic, and disulfide bonds interactions. Moreover, WPHI demonstrated significant immunomodulatory activity, and thermal and digestive stabilities (> 93 %), but extremely poor pH and salt tolerance. To address these issues, Mesona chinensis polysaccharide (MCP)-WPHI was prepared. The incorporation of MCP significantly improved the physicochemical stability of nanoparticles. Compared to WPHI, MCP-WPHI showed improved pH, thermal, salt tolerance (0-250 mM), and storage stability. This study expanded the application of WPH and MCP in delivering icariin while providing new insights for developing multifunctional high-nutritional-quality food ingredients., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

The susceptibility of bulk and exfoliated nanolayered arsenic to oxidation has been a significant obstacle limiting their widespread application and safe disposal. Here we report a controllable antimony-doped (Sb-doped) method via chemical vapor transport (CVT) with SnI 4 as a transport agent to prepare the bulk arsenic. After 96 h of exposure to air, the oxygen content on the surface of Sb-doped arsenic with SnI 4 is 67% lower compared to the undoped arsenic with SnI 4 , and 89% lower than the control group (undoped arsenic without SnI 4 ). Notably, Sb-doped arsenic is found to be easier and better exfoliated into two-dimensional (2D) nanoflakes with an average diameter of approximately 180 nm and a thickness of 4-5 nm. Sb doping reduces the surface oxygen content of exfoliated arsenic nanoflakes by 48% after 48 h of oxidation. Comprehensive experimental investigations combined with first-principles calculations demonstrate that the antioxidation improvements resulting from Sb-doping are due to the decreased adsorption energies of I 2 on the (012) and (003) surfaces of Sb-doped arsenic, while the adsorption energies of O 2 increased compared to the corresponding surfaces of undoped arsenic. The enhanced long-term stability in both bulk and layered Sb-doped arsenic presents a promising avenue for further advanced applications.

Flexible perovskite solar cells (F-PSCs) are highly promising for both stationary and mobile applications because of their advantageous features, including mechanical flexibility, their lightweight and thin nature, and cost-effectiveness. However, a number of drawbacks, such as mechanical instability, make their practical application difficult. Here, self-welding dynamic diselenide that is triggered by visible light into the structure of F-PSCs to improve their long-term stability by repairing cracks and defects in the absorber layer is incorporated. The diselenide confers the flexibility and self-welding properties to the Cs 0.05 MA 0.05 FA 0.9 PbI 3 perovskite layer, enabling optimized F-PSC devices to achieve a power conversion efficiency of 24.85% while retaining ca. 92% of their initial efficiency after undergoing 15 000 bending cycles at a curvature radius of 3 mm. The corresponding flexible large-scale module with an active area of 15.82 cm 2 achieved a record PCE of 21.65%., (© 2024 Wiley‐VCH GmbH.)

Resistive random access memory (RRAM) has emerged as a promising candidate for next-generation storage technologies due to its simple structure, high running speed, excellent durability, high integration density, and low power consumption. This paper focuses on the application of organic-inorganic hybrid perovskite (OIHP) materials in RRAM by introducing an innovative three-dimensional POPA modification strategy, which is realized by binding octa-amine-polyhedral oligomeric silsesquioxanes (8NH 2 -POSS) onto the side chains of poly(acrylic acid) (PAA), thereby enhancing the material's resilience under elevated temperatures and humidity conditions. POPA cross-links with perovskite grains at crystalline boundaries through multiple -NH 3 + and -C═O chemical anchoring sites on its branch chain, enhancing the grain adhesion, optimizing the film quality, and improving the cage structure distribution at the perovskite grain boundaries. The experimental results demonstrate that the POPA-modified OIHP RRAM exhibits an excellent resistance switching performance, with an optimal ON/OFF ratio of 5.0 × 10 5 and a data retention time of 10 4 , indicating good stability. Furthermore, the POPA modification endows the perovskite film with considerable flexibility, maintaining stable resistance switching performance under various bending radii. This study provides a vital reference for flexible, high-performance, and long-lifespan perovskite memory devices.5 , indicating good stability. Furthermore, the POPA modification endows the perovskite film with considerable flexibility, maintaining stable resistance switching performance under various bending radii. This study provides a vital reference for flexible, high-performance, and long-lifespan perovskite memory devices.

We develop a dynamics-based model of discrete movement for lateral manual interception capable of generating movements with realistic kinematics. For the present purposes, we focus on the situation of to-be-intercepted targets moving at constant speed along rectilinear trajectories oriented orthogonally with respect to the interception axis. The proposed phenomenological model is designed to capture the time evolution of empirically observed hand movements along the interception axis under different conditions of target arrival location and target speed-induced time pressure. Pattern formation dynamics combine a Duffing stiffness function, allowing for creating a fixed-point attractor at the perceived location of the target arrival on the interception axis, with a hybrid Rayleigh plus Van der Pol damping function. After parametrizing the model for required movement direction (left/right), amplitude, and duration, it adequately reproduces the (variations in) empirically observed kinematics with a single set of four coefficients for all conditions considered. The model is also demonstrated to inherently incorporate speed-accuracy trade-off characteristics.

In recent years, self-assembled monolayers (SAMs) anchored on metal oxides (MO) have greatly boosted the performance of inverted (p-i-n) perovskite solar cells (PVSCs) by serving as hole-selective contacts due to their distinct advantages in transparency, hole-selectivity, passivation, cost-effectiveness, and processing efficiency. While the intrinsic monolayer nature of SAMs provides unique advantages, it also makes them highly sensitive to external pressure, posing a significant challenge for long-term device stability. At present, the stability issue of SAM-based PVSCs is gradually attracting attention. In this review, we discuss the fundamental stability issues arising from the structural characteristics, operating mechanisms, and roles of SAMs, and highlight representative works on improving their stability. We identify the buried interface stability concerns in three key aspects: 1) SAM/MO interface, 2) SAM inner layer, and 3) SAM/perovskite interface, corresponding to the anchoring group, linker group, and terminal group in the SAMs, respectively. Finally, we have proposed potential strategies for achieving excellent stability in SAM-based buried interfaces, particularly for large-scale and flexible applications. We believe this review will deepen understanding of the relationship between SAM structure and their device performance, thereby facilitating the design of novel SAMs and advancing their eventual commercialization in high-efficiency and stable inverted PVSCs., (© 2024 Wiley‐VCH GmbH.)

Two-dimensional halide perovskites are promising for advanced photonic, optoelectronic, and photovoltaic applications. However, their long-term stability is still a critical factor limiting their implementation into further commercial applications. Here, we present an environmental stability analysis of BA 2 (MA) n- 1 Pb n I 3 n +1 (BA = C 4 H 12 N + , MA = CH 6 N + ) two-dimensional perovskites with the lowest quantum well thicknesses of n = 1 and n = 2, after 1 year of aging under ambient humidity, oxygen content, and light conditions. We observed that both crystal phases ( n = 1 and 2) degraded similarly, resulting in the removal of organic components and crystal decomposition into PbI 2 , Pb oxides, and Pb hydroxides. However, we have found a significant difference between their aging under ambient light and dark conditions, affecting their degraded morphology and photoactivity. Both crystal phases exposed to ambient light aged into a morphology characterized by the formation of several pinholes and voids, accompanied by photoluminescence degradation. Samples stored under dark conditions surprisingly preserved their photoluminescence activity, which morphologically aged into microrod structures. We conclude that the observed loss of photoactivity of 2D perovskites aged under ambient light is attributed to photoaccelerated degradation processes causing faster crystal surface photo-oxidation accompanied by a creation of multiple I vacancies and hydration of the inner crystal. The retainment of photoactivity in 2D perovskites aged under dark conditions is attributed to slower surface oxidation processes into Pb salts, as confirmed by X-ray photoemission spectroscopy. The formed surface layer even allows for a layer-by-layer degradation and acts as a protection barrier against further additional loss of I atoms and the consequent hydration of the inner part of samples. We demonstrate that light is the most critical external factor accelerating 2D perovskite degradation processes in ambient air and thus affecting their long-term stability. We conclude in this work that perovskite material structural engineering together with their surface passivation or encapsulation strategical techniques applied is an essential step for their further application into long-term stable commercial devices.

Nitrogen-rich energetic materials are of interest due to their potential use as high-energy-density materials in various applications. However, most compounds with a high nitrogen content show poor thermal stabilities, which may limit their use in certain applications. In pursuit of nitrogen-rich energetic materials, this study presents the synthesis and characterization of two nitrogen rich energetic compounds, namely 3-azido-1-(1 H -tetrazol-5-yl)-1 H -1,2,4-triazol-5-amine ( 3 , C 3 H 3 N 11 , N%: 79.78) and ( E )-1,2-bis(3-azido-1-(1 H -tetrazol-5-yl)-1 H -1,2,4-triazol-5-yl) diazene ( 7 , C 6 H 2 N 22 , N%: 80.62). Compounds 3 and 7 have high thermal stabilities of 216 and 221 °C, respectively, making them the most thermally stable among metal-free primary explosives. Additionally, they show good energetic performance ( v D : 8345 m s -1 ; P : 25.17 GPa; v D : 8275 m s -1 ; P : 25.57 GPa), making them potential candidates for metal-free high energy primary explosive. The energetic salts of 3 and 7 were also investigated. Among them, hydrazinium salt 11 displays better energetic performance ( v D : 9089 m s -1 ; P : 30.55 GPa), which was on par with those of cyclotetramethylene tetranitramine (HMX). This research contributes to the exploration of nitrogen-rich energetic materials with potential applications in various fields.

Microbial amylases should essentially remain active at higher temperatures, and in the alkaline pH and a range of surfactants to be suitable as detergent additives. In the present study, a thermophilic amylase producing bacterium, Bacillus licheniformis UDS-5 was isolated from Unai hot water spring in Gujarat, India. It was identified as a potent amylase producer during starch plate-based screening process. Therefore, the physicochemical parameters influencing amylase production were optimized using Plackett-Burman design and Central Composite Design. The amylase was purified through ammonium sulfate precipitation, size exclusion and ion exchange chromatography, achieving the purification fold and yield to be 9.2 and 40.6%, respectively. The enzyme displayed robust stability and activity across a wide range of temperatures and pHs, with an increased half-life and reduced deactivation rate constant. The amylase exhibited optimal catalysis at 70 °C and pH 8. The kinetic studies revealed Km and Vmax values of 0.58 mg/mL and 2528 μmol/mL/min, respectively. Besides, the purified amylase displayed stability in the presence of various metal ions, surfactants, and chelators suggesting its potential for industrial applications, particularly in the detergent industry. Moreover, detergent application studies demonstrated its efficacy in enhancing washing performance. A comparative profile on washing efficiency of the studied amylase and the commercial amylase with various detergents pointed towards its possible future use as a detergent additive., Competing Interests: Declarations Conflict of interest The authors declare no conflict of interest. Research involving human participants and/or animals This article does not contain any studies with human participants and/or animals performed by any of the authors., (© 2024. The Author(s), under exclusive licence to Springer Nature B.V.)

The human carbonic anhydrase II (HCA II) enzyme is a cytosolic protein located in the membrane of red blood cells that reversible hydration of carbon dioxide (CO 2 ). Considering the critical role of the HCA II and the effects of some mutations on the activity and stability of the enzyme in humans, several computational methods are used to study the structure and dynamics of the wild-type and the mutant enzymes with three ligands, CO 2 , 4-nitrophenyl acetate and acetazolamide. Our results of MD simulation of a wild-type enzyme with 4-nitrophenyl acetate show that it created essential effects on the fluctuation of this enzyme and made it more unstable and less compact than the same enzyme without ligand. In the MD of the mutant enzyme with 4-nitrophenyl acetate ligand, no significant difference is observed between with and without ligand. The affinity of the wild-type enzyme to the 4-nitrophenyl acetate is notably higher than the mutant enzyme with the same ligand. Furthermore, results showed that wild-type and mutant enzymes with CO 2 are more favorable in stability and flexibility than the same enzymes without ligand. The MD results of wild-type with acetazolamide indicate instability compare without ligand, but in MD of mutant enzyme with acetazolamide show that it more stable and compact than the same enzyme without ligand. Finally, Comparing protein trajectories to assess the impact of ligands on the stability and activity of HCA II enzymes can have medical applications and can in the engineering and design of new variants of carbonic anhydrase enzyme., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Valosin-containing protein (VCP) plays a crucial role in various cellular processes, yet the molecular mechanisms and structural dynamics of its double-psi β-barrel (DPBB) domain, particularly in human, remain insufficiently explored. While previous studies have characterized the VCP_DPBB domain in other organisms, such as thermoplasma acidophilum and methanopyrus kandleri, its evolutionary conservation, binding potential, and stability in human require further investigation. To address this gap, we first employed all-atom molecular dynamics (AAMD) simulations to examine the structural dynamics of the human VCP_DPBB domain. We also assessed its amino acid interaction energies, stability, folding enthalpy, evolutionary conservation, solubility, and crystallizability using various computational frameworks. Additionally, to uncover the plausible biological function, protein-peptide docking was performed to evaluate the interactions between the DPBB domain and the C-terminal gp78 peptide of the E3 ubiquitin ligase. Further, AAMD and coarse-grained molecular dynamics (CGMD) simulations explored the binding preferences, fluctuations, and stability of human VCP_DPBB-gp78 complexes. Our findings indicate that, while thermoplasma acidophilum VCP_DPBB-gp78 showed stronger initial binding, the human VCP_DPBB-gp78 complex exhibited superior stability, binding affinity, and more stabilizing interactions. This integrated analysis provides valuable insights into the evolutionary significance and functionality of the DPBB domain, with potential therapeutic implications for VCP-related diseases., Competing Interests: Declaration of competing interest There are no conflicts to declare., (Copyright © 2024. Published by Elsevier B.V.)

Dipalmitoylphosphatidylcholine liposomes were encapsulated with free stigmasterol (ST), stigmasteryl myristate (ME), and stigmasteryl oleate (OE). Their quality was determined using TEM, FT-IR spectroscopy, zeta potential and hydrodynamic diameter. The prepared liposomes were heated at 60 and 180 °C. The degradation of stigmasterol, fatty acids was determined, as was the formation of derivatives. The results show that the liposomes had been prepared successfully. The ST liposomes were the smallest, while the ME and OE liposomes were of similar size. The extent to which the compounds encapsulated in the liposomes degraded depended on their structure. When samples were heated to 60 °C, the degradation of stigmasterol ranged from 11 % in ST to 47 % in OE and 58 % in ME. After heating to 180 °C, the lowest level of degradation of stigmasterol was for OE (51 %), whereas the degradation of stigmasterol in ST and ME was 85 % and 90 %, respectively. In addition, the high level of oxyphytosterols in the samples heated to 180 °C is of concern, especially in the ST and ME samples. The level of SOP in liposomes heated to 60 °C ranged from 1.7 mg/g in liposomes encapsulated with free stigmasterol to 10.4 and 32.9 mg/g in liposomes with stigmasteryl myristate and oleate. After heating to 180 °C, the total content of SOP was much higher, ranging from 68.2 for OE to 111.7 and 135.7 mg/g for ME and ST, respectively., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Although metal halide perovskites are positioned as the most powerful light-harvesting materials for sustainable energy conversion, there is a need for a thorough understanding of molecular design principles that would guide better engineering of organic hole-transporting materials, which are vital for boosting the performance and stability of perovskite solar cells. To address this formidable challenge, here, we developed a new design strategy based on the curved N-doped polycyclic aromatic hydrocarbon merged with T-shaped phenazines being decorated with (phenyl)-di- p -methoxyphenylamine (OMeTAD)─N-PAH23/24 and -3,6-ditertbutyl carbazole (TBCz)─N-PAH25/26. As N-PAH23/24 exhibited satisfying thermal stability, the comparative studies performed with various experimental and simulation methods revealed a pronounced correlation between the depth of the central cyclazine core and the form of the T-shape units. This proved to be a crucial factor in controlling their π-π intermolecular interaction as well as self-assembly behavior with the perovskite layer, leading to enhanced humidity resistance, operational stability, and a maximum power conversion efficiency of 20.39% denoted for N-PAH23, which is superior to the benchmarked device with doped spiro-OMeTAD (19.23%). These studies not only resulted in optimized stability and device performance but also opened a conceptually new chemical space in the photovoltaic technology.

Aggregation of TDP-43 is linked to the pathogenesis of many neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). Notably, electrostatic point mutations such as D169G and P112H, located within the highly conserved functional tandem RNA recognition motif (RRM) domains of the TDP-43 protein (TDP-43 tRRM ), have been identified in diseased patients as well. In this study, we address how the electrostatic mutations alter both the native state stability and aggregation propensity of TDP-43 tRRM . The mutants D169G and P112H show increased chemical stability compared to the TDP-43 tRRM at physiological pH. However, at low pH, both the mutants undergo a conformational change to form amyloid-like fibrils, though with variable rates─the P112H mutant being substantially faster than the other two sequences (TDP-43 tRRM and D169G mutant) showing comparable rates. Moreover, among the three sequences, only the P112H mutant undergoes a strong ionic strength-dependent aggregability trend. These observations signify the substantial contribution of the excess charge of the P112H mutant to its unique aggregation process. Complementary simulated observables with atomistic resolution assign the experimentally observed sequence-, pH-, and ionic strength-dependent aggregability pattern to the degree of thermal lability of the mutation site-containing RRM1 domain and its extent of dynamical anticorrelation with the RRM2 domain whose combination eventually dictate the extent of generation of aggregation-prone partially unfolded conformational ensembles. Our choice of a specific charge-modulated pathogenic mutation-based experiment-simulation-combination approach unravels the otherwise hidden residue-wise contribution to the individual steps of this extremely complicated multistep aggregation process.

The success of modern biopharmaceutical products depends on enhancing the stability of protein therapeutics. Freezing and thawing, which are common thermal stresses encountered throughout the lifecycle of drug substances, spanning protein production, formulation design, manufacturing, storage, and shipping, can impact this stability. Understanding the physicochemical and molecular behaviors of components in biological drug products at temperatures relevant to manufacturing and shipping is essential for assessing stability risks and determining appropriate storage conditions. This study focuses on the stability of high-concentration monoclonal antibody (mAb) pembrolizumab, the drug substance of Keytruda (Merck & Co., Inc., Rahway, NJ, United States), and its excipients in a frozen solution. By leveraging dynamic nuclear polarization (DNP), we achieve more than 100-fold signal enhancements in solid-state NMR (ssNMR), enabling efficient low-temperature (LT) analysis of pembrolizumab without isotopic enrichment. Through both ex situ and in situ ssNMR experiments conducted across a temperature range of 297 to 77 K, we provide insights into the stability of crystalline pembrolizumab under frozen conditions. Importantly, utilizing LT magic-angle spinning (MAS) probes allows us to study molecular dynamics in pembrolizumab from room temperature down to liquid nitrogen temperatures (<100 K). Our results demonstrate that valuable insights into protein conformation and dynamics, crystallinity, and the phase transformations of excipients during the freezing of the formulation matrix can be readily obtained for biological drug products. This study underscores the potential of LT-MAS ssNMR and DNP techniques for analyzing protein therapeutics and vaccines in frozen solutions.

Quantitative analysis of peptides in biological fluids offers a high diagnostic and prognostic tool to reflect the pathophysiological condition of the patient. Recently, methods based on liquid chromatography coupled with mass spectrometry (LC-MS) for the quantitative determination of intact peptides have been replacing traditionally used ligand-binding assays, which suffer from cross-reactivity issues. The use of "top-down" analysis of peptides is rapidly increasing since it does not undergo incomplete or non-reproducible digestion like "bottom-up" approaches. However, the low abundance of peptides and their peculiar characteristics, as well as the complexity of biological fluids, make their quantification challenging. Herein, the analytical pitfalls that may be encountered during the development of an LC-MS method for the analysis of intact peptides in biological fluids are discussed. Challenges in the pre-analytical phase, stability after sampling and sample processing, significantly impact the accuracy of peptide quantification. Emerging techniques, such as microextractions, are becoming crucial for improved sample cleanup and enrichment of target analytes. A comparison between the roles of high-resolution and low-resolution mass spectrometry in the quantification of intact peptides, as well as the introduction of supercharging reagents to enhance ionization, will be discussed.

Hole-transporting material (HTMs) are crucial for obtaining the stability and high efficiency of perovskite solar cells (PSCs). However, the current state-of-the-art n-i-p PSCs relied on the use of 2,2',7,7'-tetrakis(N,N-di-p-methoxyphenylamine)-9,9'-spirobifluorene (spiro-OMeTAD) exhibit inferior intrinsic and ambient stability due to the p-dopant and hydrophilic Li-TFSI additive. In this study, a new spiro-type HTM with a critical quasi-planar core (Z-W-03) is developed to improve both the thermal and ambient stability of PSCs. The results suggest that the planar carbazole structure effectively passivates the trap states compared to the triphenylamine with a propeller-like conformation in spiro-OMeTAD. This passivation effect leads to the shallower trap states when the quasi-planar HTMs interact with the Pb-dimer. Consequently, the device using Z-W-03 achieves a higher V oc of 1.178 V compared to the spiro-OMeTAD's 1.155 V, resulting in an enhanced efficiency of 24.02 %. In addition, the double-column π-π stacking of Z-W-03 results in high hole mobility (~10 -4  cm 2  V -1  s -1 ) even without p-dopant. Moreover, when the surface interface is modified, the undoped Z-W-03 device can achieve an efficiency of nearly 23 %. Compared to the PSCs using spiro-OMeTAD, those with Z-W-03 exhibit enhanced stability under N 2 and ambient conditions. This superior performance is attributed to the quasi-planar core structure and the presence of multiple CH/π and π-π intermolecular stacking in Z-W-03. The multiple CH/π and π-π intermolecular contacts of HTMs can improve the hole hopping transport. Therefore, it is imperative to focus on further molecular structure design and optimization of spiro-type HTMs incorporating quasi-planar cores and carbazole moieties for the commercialization of PSCs., (© 2024 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.)

The development of stable water-in-oil-in-water (W/O/W) emulsions for edible preservation coatings and films, utilizing their properties, deserves scientific attention. In this study, oregano essential oil and D‑sodium erythorbate were simultaneously loaded into W/O/W emulsions, and the homogenization conditions of the W/O/W emulsions were optimized. The structure and interactions of gum Arabic (GA) and whey protein isolate (WPI) as the outer phase were analyzed. Stable W 1 /O/W 2 emulsions with excellent antimicrobial and antioxidant activities could be produced under the conditions of GA: WPI at 1:1 and W 2 : W 1 /O at 5:5. The diphenyl-1-picrylhydrazyl radical (DPPH) and 2,2'-azinobis-(3-ethylbenzenthiazoline-6-sulphonic acid) (ABTS) radical scavenging rates were 86.35 % and 89.35 %, and the inhibition zone diameters for S. aureus and E. coli were 14.03 ± 0.42 mm and 14.17 ± 0.70 mm, respectively. Finally, the W 1 /O/W 2 emulsions were successfully applied to prepare chitosan-based films. This study has the potential to promote the application of W/O/W emulsions in food preservation, emphasizing the need for advancements for real-world adaptability., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

Aim: This study aimed to investigate the biomechanical properties of 60 % carbon fiber-reinforced polyetheretherketone (Cfr-PEEK), which exhibits high mechanical strength and can address the limitations of titanium mini plates used in Le Fort I osteotomy., Material and Method: Models were created using the FEA method based on tomography images of adult individuals. A 5 mm maxillary advancement was applied to the models following Le Fort I osteotomy. Mini plates made of titanium and 60 % Cfr-PEEK were used. Support was provided by the nasomaxillary and zygomaticomaxillary buttresses to fix a total of four l-shaped mini plates. Oblique loads of 125 N, directed from palatal to buccal, and a total of 250 N compression loads were applied to the central fossa of the premolar and molar teeth in the maxillary model at a 30° angle relative to the long axis of the teeth. Displacement values at the osteotomy line, Von Mises stresses in the mini plate-screws, and principal stresses in the bone were compared., Results: Examination of stress values in the fixation systems of the models revealed higher stress values in the Cfr-PEEK model compared to the titanium model. However, these stresses did not reach levels that would deform the Cfr-PEEK fixation systems. Stress and displacement values in the bone were lower in the Cfr-PEEK model compared to the titanium model., Conclusion: According to the findings of our study, Cfr-PEEK represents a viable alternative to titanium for mini plate material in Le Fort I osteotomy, offering biomechanical advantages., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Masson SAS. All rights reserved.)

Guayabo plantain (GP) starch was chemically modified by acetylation to evaluate its role as a stabilizer and emulsifier in low-fat dressings. Native starch (NS) from GP was chemically modified starch (MS), and its functional properties, such as water absorption index, water solubility index, swelling power, gelatinization temperature ( T ), were evaluated. Additionally, functional groups and morphology were identified using Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy. Low-fat dressings were prepared using NS and MS at two concentrations, 2% and 3% (NS2, NS3, MS2, MS3), and the stability of the dressings was evaluated over a storage period of 28 days at 4 °C ± 2.0 °C. The percentage of acetylation and the degree of substitution obtained were 2.48% and 0.01, respectively, complying with current regulations. MS showed a higher amylose content (23.62 ± 1.89%) than NS (16.01 ± 0.43%). The g ), were evaluated. Additionally, functional groups and morphology were identified using Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy. Low-fat dressings were prepared using NS and MS at two concentrations, 2% and 3% (NS2, NS3, MS2, MS3), and the stability of the dressings was evaluated over a storage period of 28 days at 4 °C ± 2.0 °C. The percentage of acetylation and the degree of substitution obtained were 2.48% and 0.01, respectively, complying with current regulations. MS showed a higher amylose content (23.62 ± 1.89%) than NS (16.01 ± 0.43%). The T in the FT-IR spectra suggested a modification in the functional characteristics of starch due to acetylation. Emulsions of MS at 2% and 3% (MS2 and MS3) showed a smaller droplet size and higher interfacial dispersion. However, MS3 had higher viscosity, which contributed to an increase in hydrophobicity and delays in flocculation and subsequent coalescence. This research study provides useful information on the use of 3% MS dressings in new food formulations, reducing fat content while preserving functional characteristics, thus ensuring greater stability.g of MS decreased, and the appearance of bands at 1012 and 1723 cm -1 in the FT-IR spectra suggested a modification in the functional characteristics of starch due to acetylation. Emulsions of MS at 2% and 3% (MS2 and MS3) showed a smaller droplet size and higher interfacial dispersion. However, MS3 had higher viscosity, which contributed to an increase in hydrophobicity and delays in flocculation and subsequent coalescence. This research study provides useful information on the use of 3% MS dressings in new food formulations, reducing fat content while preserving functional characteristics, thus ensuring greater stability., Competing Interests: DECLARATION OF CONFLICTING INTERESTSThe authors declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: The authors have no actual or potential conflict of interest that could inappropriately influence their research. The authors have conducted themselves within the bounds of ethical behaviors. This is an original work. However, the work and the words of other authors have been cited according to the references. All authors have seen and approved the final version of the paper and consented to its submission for publication.

Polysorbates, widely used excipients in drug formulations, present a stability challenge due to complex degradation processes. This study investigates the hydrolysis of polysorbate (PS) under temperature stress (50 °C), focusing on the impact of primary packaging materials (glass vs. plastic vials), buffers (histidine and acetic acid), counterions (chloride vs. malate), and pH (4-7). Our findings reveal that leachables from plastic vials inhibit PS degradation in both histidine and acetic acid buffers. Kinetic parameters derived from sigmoidal fitting suggest distinct degradation mechanisms for each buffer. Furthermore, the malate counterion with histidine displays inhibitory effects on PS hydrolysis. Principal component analysis was employed to identify key factors. These results highlight the critical role of excipients and packaging in PS stability, providing valuable insights for biopharmaceutical formulation development and a deeper understanding of PS degradation complexities., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.)

Advances in gene therapy, exemplified by mRNA vaccines against COVID-19, highlight the importance of lipid nanoparticles (LNPs) for nucleic acid delivery despite challenging storage conditions. Substituting mRNA with pDNA in LNPs may enhance stability and efficacy, yet maintaining LNP stability poses challenges, particularly during freeze-drying. Cryoprotectants offer potential to mitigate destabilization, improving LNP properties and in vivo performance. Here, we evaluated the effects of different concentrations of various cryoprotectants on the freeze-drying process of pDNA-loaded LNPs, assessing their physicochemical characteristics and transfection efficiency. Stability was examined under various storage conditions, confirming biological efficacy post-storage. Our results highlight the role of cryoprotectants in optimizing freeze-drying for the extended shelf life of nucleic acid-loaded LNPs. Trehalose emerged as an efficient cryoprotectant, maintaining LNP stability after the freeze-drying process for up to 2 years, with diameters and transfection efficiency comparable to fresh formulations. These findings demonstrate the optimized concentration of cryoprotectants to sustain LNP stability despite freeze-drying and prolonged storage, providing valuable insights for nucleic acid-based therapies., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

The aim of this study was to prepare sodium glycocholate liposomes (SGC-Lip) encapsulating semaglutide (Sml) to improve oral bioavailability and better exert hypoglycemic effect. In this paper, SGC-Lip was prepared by reverse-phase evaporation method with particle size around 140 nm, potential around -27 mV, rounded morphology and better stability. The hypoglycemic and intestinal uptake effects of SGC-Lip and cholesterol-containing liposomes (CH-Lip) were comparatively investigated in rats, and the oral safety of SGC-Lip was examined by cytotoxicity assay. The results indicate that SGC-Lip can achieve a hypoglycemic effect of 40% of the initial value within 12 hours, and the AAC 0-12h is approximately six times that of CH-Lip without sodium glycocholate. The results of the cytotoxicity tests indicate that SGC-Lip has good oral safety. SGC-Lip enhances the absorption of semaglutide in the small intestinal villi via an apical sodium-dependent bile acid transporter (ASBT)-mediated pathway with the highest penetration at the ileal site. In summary, the oral bioavailability of semaglutide can be improved by encapsulating semaglutide in SGC-Lip and utilizing the stabilizing and permeation-promoting effects of SGC on liposomes., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Anthocyanin (ACN) has attracted considerable attention due to its wide range of physiological effects. However, challenges such as poor stability and limited bioavailability have hindered its utilization in functional foods. To address these issues, this research utilized milk-derived extracellular vesicles (MEV) as carriers for encapsulating and binding ACN through various techniques, including ultrasonic, electroporation, saponin treatment, incubation, and freeze-thaw cycles. The objective of these approaches was to enhance the stability of ACN and improve its oral delivery. Notably, the ACN-loaded MEV (MEV-ACN) prepared through ultrasonic exhibited small particle sizes and good stability under processing, storage, and simulated digestion conditions. Cellular studies revealed that MEV-ACN exhibited pro-oxidant properties and induced oxidative stress, leading to cell apoptosis with greater efficacy compared to free ACN. These findings suggest that encapsulating ACN within MEV can significantly enhance its processing and oral stability, as well as strengthening its dietary defense capabilities in anti-tumor applications., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Ltd.)

Procyanidin B2 (Pac B2) has attracted much attention due to its strong antioxidant activity, but poor in vivo stability limits its wide application in food and medicine. In this paper, composite nanoparticles (NPs) were constructed using abietic acid (AA) as a carrier, which significantly enhanced Pac B2 stability. A spherical morphology and average diameter of 396.05 nm were observed in AA-Pac B2 NPs synthesized by solvent co-precipitation. Pac B2 encapsulation was 11.28 %, and thermal stability is improved. Infrared, Ultraviolet spectrum, and MD (molecular dynamics) spectroscopy revealed hydrogen bonding and hydrophobic interaction between AA and Pac B2. For up to 2 h at 37 °C, Pac B2 can be sustainably released in simulated gastric and intestinal fluids. In vitro, AA-Pac B2 NPs at the same concentration exhibited higher bioavailability and uptake efficiency than free Pac B2. The data demonstrate the potential of AA NPs for improving polyphenol thermal stability and bioavailability., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

A compact antioxidant interfacial layer was fabricated by combining phosphorylation treatment with protocatechuic acid (PA) copolymerization to enhance the physical and oxidative stability of high internal phase emulsions (HIPEs) prepared using perilla protein isolate (PPI). The covalent binding between PPI and phosphate groups induced conformational changes, facilitating the interaction between PPI and PA. The formed phosphorylated PPI-PA conjugates (LPPI-PA) exhibited a reduced particle size of 196.75 nm, promoting their adsorption at the interface. HIPEs prepared by LPPI-PA conjugates showed higher storage stability due to decreased droplet size, increased interfacial protein adsorption content (90.48%), and the formation of an interconnected network within the system. Additionally, the combination of LPPI and PA anchored PA to the interface, significantly inhibiting lipid oxidation in HIPEs as evidenced by low levels of lipid hydroperoxide (30.33 μmol/g oil) and malondialdehyde (379.34 nmol/g oil). This study holds significant implications for improving the stability of HIPEs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier Ltd.)

With the intensification of climate change and human activities, wetland ecosystem and their carbon pool function have been seriously compromised. To determine the soil organic carbon pool composition and stability response to wetland disturbance, three disturbed (grazing, mowing, invasion) and two undisturbed Carex tussock wetlands were investigated in Momoge Wetland, northeast China. The results showed that the disturbance significantly reduced the soil organic carbon content under hummock, but effectively promoted organic carbon storage in surface soil in hummock interspace. In disturbed wetlands, relative abundance of aromatic-C, asymmetric aliphatic-C, polysaccharide-C and clay minerals, and organic carbon stability significantly declined. Furthermore, asymmetric aliphatic-C and polysaccharide-C were the most important organic carbon chemical components affecting SOC stability under hummock and in hummock interspace. Disturbance facilitated the effects of pH, TP and minerals on organic carbon stability, with pH being the most important. These findings improved our understanding of the composition and stability of carbon pools in disturbed wetlands., Competing Interests: Declaration of competing interest The authors declare that they have no conflicts of interest., (Copyright © 2024. Published by Elsevier B.V.)

Afterglow materials face limitations in color variety, low luminosity, and stability. Thus, developing materials with adjustable afterglow color, increased photoluminescence (PL) intensity, and enhanced stability is crucial. This paper reports the fabrication of a series of core-shell composites, CPB@SMSO@SiO 2 , which combine Sr 2 MgSi 2 O 7 : Eu 2+ , Dy 3+ (SMSO) and lead halide perovskite quantum dots (CsPbBr 3 /CPB PeQDs) through a process involving in-situ growth and hydrolytic coating. The SMSO in the composite can absorb 365 nm UV light and then emit 470 nm light, which can be absorbed by the CsPbBr 3 PeQDs, resulting in an overall increase in the PL intensity of the composite. The afterglow color can be turned from green to blue by adjusting the ratio of SMSO and CsPbBr 3 . Furthermore, the stability of the composites is improved by the SiO 2 shell layer formed by hydrolysis of tetramethyl orthosilicate (TMOS). This study presents an opportunity to develop innovative afterglow materials., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Alginate (Alg) hydrogels have demonstrated great potential in drug delivery, wound dressings, and tissue engineering. However, the practical applications of conventional Alg hydrogels suffer from rapid degradation, insufficient controlled drug release, and poor adhesion to tissues. In this paper, the physicochemical properties of Alg hydrogels were comprehensively modulated through chemical modification and the incorporation of various polymers. The results showed that introducing neutral polymers stabilized Alg hydrogels at room temperature. However, this stabilizing effect did not persist at 37 °C. The cationic chitosan (CS) can bind to Alg through electrostatic interaction. The incorporation of CS substantially improved the stability of Alg hydrogels and remarkably prolonged the release of BSA from hydrogels to 14 days at 37 °C. Meanwhile, introducing dopamine (DA)-modified Alg enhanced the adhesion of hydrogel to porcine skin. The optimized hydrogels were utilized to encapsulate platelet-rich plasma (PRP). The PRP-loaded composite hydrogel (2 wt% Alg, with a Ca 2+ /carboxyl group molar ratio of 0.2, a DA/carboxyl group molar ratio of 0.2, and a CS content of 30 % of Alg) exhibited an excellent therapeutic effect in the healing of rabbit shoulder cuff injury. These findings provide valuable insights into the modulation of physicochemical properties of hydrogels for biomedical applications., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

In this paper, we analyze the role of fear in a three-species non-delayed ecological model that examines the interactions among susceptible prey, infectious (diseased) prey, and predators within a food web. The prey population grows in a logistic manner until it achieves a carrying capacity, reflecting common population dynamics in the absence of predators. Diseased prey is assumed to transmit infection to healthful prey by the use of a Holling type II reaction. Predators, alternatively, are modeled to consume their prey using Beddington--DeAngelis and Crowley--Martin response features. This evaluation specializes in ensuring the non-negativity of solutions, practical constraints on population dynamics, and long-term stability of the system. Each biologically possible equilibrium point is tested to understand the environmental stable states. Local stability is assessed through eigenvalue analysis, while global stability of positive equilibria is evaluated by the use of Lyapunov features to determine the overall stability of the model. Furthermore, Hopf bifurcation is explored primarily based on infection rate $\varepsilon$. Numerical simulations are carried out to validate the theoretical effects and offer practical insights into the model behaviour under specific conditions., (Creative Commons Attribution license.)

This study focuses on solving the Caudrey-Dodd-Gibbon ( CDG ) equation using the Khater II ( KII ) method and the Variational Iteration ( V I ) method. The CDG equation is a pivotal mathematical model in nonlinear wave dynamics, essential for understanding the evolution, interaction, and preservation of wave forms in dispersive media. Its applications span various fields, including fluid dynamics, nonlinear optics, and plasma physics, where it plays a crucial role in analyzing solitons and complex wave interactions. In this research, we meticulously implement the KII and V I methods to derive solutions for this nonlinear partial differential equation. Our findings reveal new aspects of the equation's behavior, offering deeper insights into nonlinear wave phenomena. The significance of this study lies in its contribution to advancing the understanding of these phenomena and their practical applications in the academic realm. The results underscore the effectiveness of the employed methods, their innovative contributions, and their relevance to applied mathematics., Competing Interests: Declarations Competing interests Te authors declare no competing interests., (© 2024. The Author(s).)

Purpose: The present study evaluated the contact angles (CAs) of four denture base materials subjected to different surface treatments using deionized water and saliva substitutes., Material and Methods: A total of 32 rectangular specimens were manufactured using four different denture base materials: heat-cured compression molded Lucitone 199 (C), milled Lucitone 199 (M), Formlabs Denture Base RP (P), and SR Ivocap High Impact (I). The CA of the surface of the unaltered, mechanically polished, and sandblasted surface specimens was evaluated after the application of five saliva substitutes: Biotene, VEGA, Spry, Moi-Stir, Dentilube, and ionized water. Ten droplet measurements were obtained for each group, with each droplet analyzed for advancing contact angle (ACA), receding contact angle (RCA), and the contact angle hysteresis (CAH) was calculated. The data of the experiment was analyzed using 2-way ANOVA, (α = 0.05) with Tukey's test., Results: CAH was demonstrated to have statistically significant differences among the denture bases (p < 0.05), with unaltered 3D printed exhibiting the largest CAH, followed by unaltered milled. The unaltered denture bases exhibited higher CAH than the polished, and there were no significant differences in CAH among the polished denture bases (p > 0.05). Sandblasting increased the ACA of the milled and conventional bases. The saliva substitutes exhibited differences in ACA, with Spry and VEGA having the highest ACA, and Biotene had the lowest CA of all the saliva substitutes evaluated., Conclusion: The manufacturing methods of denture bases influences the CAH, while the chemical composition of the denture base specimens does not appear to affect CAH. Sandblasting increases the ACA for the milled and conventional groups. Saliva substitutes do impact the ACA. Drawing from previous research, it is hypothesized that a 3D-printed denture base or sandblasting a milled denture base may offer greater resistance to dislodgement., (© 2024 The Author(s). Journal of Prosthodontics published by Wiley Periodicals LLC on behalf of American College of Prosthodontists.)

Background: The measurement of neurofilament light (NFL) in blood samples has been established as a sensitive measure of neuroaxonal damage in a wide range of diseases in the peripheral and central nervous system, including multiple sclerosis (MS). Previous studies have identified confounding factors that may influence the serum concentration of NFL., Aim: We aimed at investigating the relationship between known confounders (age, body mass index, blood volume) and risk factors for MS (smoking and human leukocyte antigen (HLA)) on serum concentrations of NFL in control subjects. In addition, we compared different methods for correction for confounders when applied to newly diagnosed patients with MS., Methods: We measured serum concentrations of NFL by single molecule array analysis in 1.101 control subjects without neurological disease from 4 different cohorts (including 906 healthy blood donors) and 72 patients with newly diagnosed relapsing-remitting MS. A questionnaire on smoking habits was distributed to the 906 healthy blood donors, and the HLA risk alleles HLA-DRB1*15:01 and HLA-A*02:01 were genotyped by TaqMan allelic-discrimination PCR analysis in these subjects., Results: We confirmed that serum concentrations of NFL increase with age, but we also found that sample storage conditions for the different cohorts of control subjects had a substantial effect. Prolonged storage time and storage at -20° were independently associated with lower serum concentrations of NFL than shorter storage time and storage at -80° In samples from the large cohort of blood donors, we confirmed an association between high BMI and high blood volume with lower serum concentrations of NFL and found that this association was marginally stronger for BMI than for blood volume. We found no association between smoking and HLA risk factors for MS with serum concentrations of NFL in the blood donor cohort. Finally, we found that a simple method for correcting for the effect of age on NFL performed as well as Z-scores, which consider the effect of both age and BMI. This was shown when discriminating between patients with MS and control subjects and between MS patients with and without Gd-enhancing MRI lesions., Conclusions: We confirm an association between serum concentrations of NFL, age, and BMI, but we also find that it may often be sufficient to correct for the effect of age alone. The effect of BMI should, however, be considered along with the effect of other confounding factors, including various comorbidities., Competing Interests: Declaration of competing interest Helle Bach Søndergaard, Anna Olsson, Cecilie Ammitzbøll, Lise Wegner Thørner, Erik Sørensen, Marie Krogh Nielsen, Josefine Britze, Signe Modvig, Poul Erik Hyldgaard Jensen, Torben Lykke Sørensen, Annette Bang Oturai have nothing to declare. Stefan Gustavsen has received support for congress participation from Merck and Sanofi. Finn Sellebjerg has served on scientific advisory boards for, served as consultant for, received support for congress participation or received speaker honoraria from Alexion, Biogen, Bristol Myers Squibb, Lundbeck, Merck, Novartis, Roche and Sanofi Genzyme. His laboratory has received research support from Biogen, Merck, Novartis, Roche and Sanofi Genzyme., (Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.)

This study explored the feasibility of depositing protective coatings with an Sb scavenger function on mine waste rocks derived from the exploitation of stibnite deposits. Encapsulation treatments were performed using ferrous sulfate as the coating precursor. Different Fe/Sb leachable molar ratios (0.1, 1, and 10) were evaluated using hydrothermal and thermal processes at various temperatures (30, 50, 100, and 150 °C). The environmental characterization of the coated mine waste was established using standard leaching tests. The most effective coatings were analyzed for their mineralogy, chemical composition, and Sb attenuation using X-ray powder diffraction, scanning electron microscopy, and digestion/extraction processes. Additionally, stability tests were conducted to assess the effectiveness of encapsulation under changing environmental conditions. The Fe/Sb leachable molar ratio was found to be a critical factor in reverting the toxic and hazardous characteristics of mine wastes, with an optimal value of 10. The coatings were primarily composed of Fe oxyhydroxy sulfates/Fe oxyhydroxides and calcium sulfate minerals with a bulk Sb content of approximately 1 %. The adsorbed Sb content in the coatings was a small fraction of the total Sb content (< 0.5 %), indicating a strong retention. Moreover, such coatings were stable under different pH (3-8) and redox (100 to -100 mV) conditions., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)

With the extension of heat processing, the oxidation and formation of harmful substances in oils appeared. The effect of the high-temperature stages (180 °C, four stages I, II, III, and IV were divided according to the heating-up period) on the fatty acid profile, the thermal properties, the composition of total polar compounds, and the physicochemical properties of rapeseed oil (RSO) were investigated. As the heating processing, carnosic acid (CA) significantly reduces the peroxide value, p-anisidine value, trans-fatty acid, the action of alkyl radicals, and the formation of oxidized triglyceride monomers (Ox-TGM). The T p of the RSO shifts towards the lower temperature, and the enthalpy exhibits a significant decrease in stages II, III, and IV. Stage II is the crucial period for the transformation of Ox-TGM into polymers. CA helps control the oxidation process of the oil. It is essential to maintain the quality and prolong the usage time of RSO., Competing Interests: Declaration of competing interest The authors explicitly indicate that there are no potential interests and state their willingness to publish in this journal., (Copyright © 2024. Published by Elsevier Ltd.)

(-)-Epicatechin (EC) is a commonly dietary phytochemical that presents multi-physiological activities on human health. Thermal processing is a common method to extract EC, albeit likely to degrade EC considering its thermal instability. In this study, an 85-min non-durable bathing incubation assay was designed to simulate the state of EC in boiling water while cooking. Monitoring of degradation products was performed using ultra-performance liquid chromatography combined with electrospray ionization quadrupole tandem mass spectrometric detection (UPLC-ESI-TSQ-MS/MS). The results revealed that ca. 65.2 % loss of EC was detected in the first 10 min, and over 99.5 % of EC was degraded within 30 min. A total of 22 degradation products were identified based on retention time, full and tandem MS data were the first to be comprehensively reported. Isomerization, oxidation, hydroxylation, dimerization, and ring cleavage were the main chemical reactions that occurred for EC in boiling aqueous solution., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

In this research work, the authors have developed a mathematical model to examine the interaction between dystrophin protein and tumor. The authors formulated a system of ordinary differential equations to describe the dynamics of the dystrophin-tumor interaction system. Jacobian matrix and Routh-Hurwitz stability techniques were used to determine equilibrium points, perform stability and bifurcation analysis, and establish the conditions required for the stability of the proposed model. Numerical simulations are performed using Euler's method to investigate the temporal evolution of the proposed model under different parameter values, such as tumor growth rate and feedback strength of dystrophin protein. The numerical results are presented in tables, and corresponding to each table, a graphical analysis is done. The graphical analysis includes creating phase portraits to visually represent stability regions around the equilibrium points, bifurcation diagrams to identify critical points, and time series analysis to highlight the behavior of the proposed model. The authors explore how variations in dystrophin expression impact tumor progression, identifying potential therapeutic implications of maintaining higher dystrophin levels. This comprehensive analysis enhances our understanding of the dystrophin-tumor interaction, providing a basis for further experimental validation and potential therapeutic strategies., Competing Interests: Declarations Competing interests The authors declare no competing interests. Consent to participate Each author has approved of and agreed to submit the article., (© 2024. The Author(s).)

Hybrid organic-inorganic perovskite solar cells (PSCs) have shown significant potential in photovoltaic applications due to their superior optoelectronic properties. However, the conventional electron transport layer (ETL) of C 60 in PSCs poses challenges such as incomplete coverage and metal diffusion, leading to reduced performance and stability. This work explores the efficacy of atomic layer deposition (ALD) of SnO 2 as an interlayer between C 60 and electrode to enhance the performance and stability of devices. Devices with varying SnO 2 thicknesses were fabricated, revealing that a 15 nm ALD-SnO 2 layer optimally improved the power conversion efficiency (PCE) to 23.85%, compared to the 22.86% achieved with a BCP layer. Moreover, the SnO 2 -based devices exhibited superior open-circuit voltage ( V OC ), short-circuit current density ( J SC ), and fill factor (FF). Modules (30 × 30 cm) with ALD-SnO 2 is a promising interlayer candidate for PSCs, providing a pathway toward higher efficiency and stability in perovskite solar technology.2 buffer layer. This research indicates that ALD-SnO 2 is a promising interlayer candidate for PSCs, providing a pathway toward higher efficiency and stability in perovskite solar technology.

Oxide-perovskites designed for automotive catalysts contain multiple metal elements whose presence is crucial to achieving the targeted performance. They are highly stable in exhaust operating conditions; however, little is known about their stability under physiological conditions. As some of the metallic components are hazardous to humans and the environment, perovskite benefits in cleaner air must be balanced with risks in a Safe and Sustainable Design (SSbD) approach. New approach methodologies (NAMs), including in chemico and in silico methods, were used for testing hazards and benefits, including catalytic activity and tolerance for temporary excess of oxygen under dynamic driving conditions. The composition and surface properties of six different lanthanum-based oxide-perovskites compromised their stability under lung physiological conditions, influencing the oxidative damage of the particles and the bioacessibility of leaching metals. We found consistent biotransformation of the oxide-perovskite materials at pH 4.5. The leached lanthanum ions, but not other metals, respeciated into lanthanum phosphate nanoparticles, which increased the overall oxidative damage in additive synergy. The NAM results in the presented SSbD approach were challenged by in vivo studies in rats and mice, which confirmed multicomponent clearance from lungs into urine and supported the comparative ranking of effects against well-characterized spinel materials. Among the perovskites, the version with reduced nickel content and doped with palladium offered the best SSbD balance, despite not improving the conventional benchmark catalytic performance and related sustainability benefits. Redesign by industry may be necessary to better fulfill all SSbD dimensions.

Over the last few years, the influence of low temperature (≤80 °C) and, in particular, of room temperature, atomic layer deposited alumina (ALD-Al 2 O 3 ) on the properties of the underlying hybrid perovskites of different compositions and on the efficiency and stability of the corresponding perovskite solar cells (PSCs) is extensively investigated. The main conclusion is that most probably thanks to the presence of intrinsic defect states in the ALD-Al 2 O 3 and in the perovskite layers, charge transfer and neutralization are possible and the entire lifetime of the PSCs is thus improved. Moreover, the migration of mobile ions between the layers is blocked by the ALD-Al 2 O 3 layer and thus the occurrence of hysteresis in the current density-voltage characteristics of the PSCs is suppressed. Considering the uniform and nondestructive surface coverage, low thermal budget, small amount of material required, and short duration of the established ALD-Al 2 O 3 deposition on top of hybrid perovskites, this additional, but fully solar cell technology-compatible, process step is most likely the most effective, cheapest, and fastest way to improve the efficiency and long-term stability of PSCs and thus increase their marketability., (© 2024 The Author(s). Small published by Wiley‐VCH GmbH.)

Inverted perovskite solar cells (PSCs) hold exceptional promise as next-generation photovoltaic technology, where both perovskite absorbers and charge-transporting materials (CTMs) play critical roles in cell performance. In recent years, polymeric CTMs have played an important role in developing efficient, stable, and large-area inverted PSCs due to their unique properties of high conductivity, tunable structures, and mechanical flexibility. This review provides a comprehensive overview of polymeric CTMs used in inverted PSCs, encompassing polymeric hole transport materials (HTMs) and electron transport materials (ETMs). the relationship between their molecular structures, modification strategies are systematically summarized and analyzed for adjusting energy levels, and improving charge extraction, enabling a deep understanding of these widely used materials. The review also explores effective strategies for designing even more efficient polymeric CTMs. Finally, an outlook is proposed on the exciting research of novel polymeric CTMs, paving the way for their commercialized applications in PSCs., (© 2024 Wiley‐VCH GmbH.)