Interface Membrane Research Articles

Regulatory mechanism of blending additives on interface interaction and phase separation of the heterogeneous braid-reinforced hollow fiber membranes

The exfoliation of the polymer layer from the reinforcement material is the key challenge for applying braid-reinforced hollow fiber membranes (BR HFMs). In this work, a mixed amphiphilic additive system was constructed and adopted in BR HFMs preparation by non-solvent induced phase separation (NIPS). The effect of the mixed system on the state of the casting solution and phase inversion process, the interaction between the casting solution and the braid material, together with the structure and filtration performance was studied. The role of the mixed system on the interface coordination and membrane structure formation mechanisms was elucidated. The results showed that both the composition of the mixed amphiphilic additives and the interaction time between the casting solution and braid material threw much light on the interface coordination and membrane formation. The interfacial compatibility of the casting solution and braid material was obviously improved, resulting in the enhancement of the binding force between the braid and PVDF membrane layer. The permeation flux and anti-exfoliation performance were simultaneously improved with the proper addition of the mixed amphiphilic additives. The stability of the BR HFMs was primarily testified by filtration of real sludge suspension solution with back-washing operation.

Particle-stabilized foams with fatty acid salts as stabilizers triggered by transition metal ions

Particle-stabilized foams have been becoming the focus on foaming field because of their excellent stability due to the high stiffness of interface membrane. However, the modification of particle surfaces to reach an appropriate wettability needs complicated process, resulting in accompanied inconvenient foaming-defoaming regulation. In this work, we reported a series of foams stabilized by insoluble particles generated from fatty acid anions with metal ions. Different hydrocarbon chains endowed the formed particles diverse wettability and different aggregation behaviors at the gas–liquid interface, e.g., different foamability and the formation of the “dry water”. The foams exhibited ultra-stable properties and were responsive to environmental acidity, thus possessing a smart foaming-defoaming transition tuned by pH. The combination ability of fatty acid anions with metal ions changed with the chain-length and the nature of metal ions, leading to a choice for the extraction or separation of some metal ions in a fast and simple way. This new aggregation behavior of fatty acid salts can be explored to expand the practical applications.

Analysis of serum phase proteins and emulsifiers on the whipping capabilities of aerated emulsions: From the perspective of air-liquid interface rheology

In aerated emulsions, the serum phase plays a crucial role in determining whipping capabilities. However, the effects of serum phase components on emulsion properties remain largely unexplored and continue to be a mystery. This study takes a micro-level approach, focusing on the air-liquid interfacial rheology by incorporating different types of surfactants (proteins and emulsifiers) into the serum phase. It systematically explores the effects on the serum phase interface, emulsion properties, whipping capabilities, and foam stability in a stepwise manner. Proteins only slightly affect the strength of the air-liquid interface, primarily improving the capacity to trap bubbles at the initial whipping stage, thereby boosting the overrun of the aerated emulsion. The high viscoelastic modulus of the interface membrane is greatly influenced by the presence of solid lipid nanoparticles of glycerol monostearate (GMS SLN), leading to a reduction in whipping time and improved surface-mediated partial coalescence. This ultimately enhances the quality and stability of the foam system. Tween 80, due to its hydrophilic properties, is able to quickly adsorb at the air-liquid interface using the Gibbs-Marangoni mechanism. This helps to expedite the end of the whipping process and ultimately improves the foam quality. On the contrary, glycerol monooleate (GMO), a lipophilic emulsifier for liquids, struggles to effectively adsorb at the interface, leading to decreased stability of the air-liquid interface in the system and resulting in poor whipping capabilities. This paper delves into the mechanism by which different surfactants affect the whipping capabilities of aerated emulsions through an analysis of serum phase composition, laying the groundwork for enhancing formulation design.

Elucidation of microscopic mechanisms of tweens on whipping capabilities of aerated emulsions: Fat crystal-membrane interaction perspective

Aerated emulsions find wide applications in the food industry, with partial coalescence playing a crucial role as the core of such products in whipping capabilities. Although tweens are the most traditional emulsifiers used in aerated emulsions, the microscopic mechanisms of how they work are still not fully understood. This study focused on elucidating the mechanisms of Tweens in fat crystallization, oil-water interface rheology, and fat globule interface membrane properties, clarifying their roles in partial coalescence and whipping capabilities. The fat crystals induced by Tween 20 (T20) faced difficulty in puncturing the interface membrane with a high elastic modulus (5.58 mN/m), which may constrain occurrence and progression of partial coalescence. Tween 60 (T60) and Tween 40 (T40) exhibited strong interactions with proteins, with the interface film formed by T60 having a high elasticity of up to 7.79 mN/m. However, the highest elasticity interface film formed by orogenic behavior from T60 was not conducive to the interaction between fat crystals and the interfacial proteins during the whipping process. T40 not only helps to stimulate fat crystallization and create interface films with appropriate elastic strength but also plays a role in enhancing foam quality as its concentration rises. This is supported by its rheological properties and microscopic structures. The interface membrane formed by Tween 80 (T80) was viscous, leading to a significant partial coalescence but poor foam quality. This study reveals the interaction mechanisms between fat crystallization, interface membrane, partial coalescence, and the structure of aerated emulsions regulated by Tweens.

Effect of diacylglycerol on partial coalescence of aerated emulsions: Fat crystal-membrane interaction and air-liquid Interface interaction insights

Currently, the poor whipping capabilities of anhydrous milk fat (AMF) in aerated emulsion products are a major obstacle for their use in beverages like tea and coffee, as well as in cakes and desserts, presenting fresh hurdles for the food industry. In this study, the mechanism of action of diacylglycerols (DAGs) with different carbon chain lengths and degrees of saturation on the partial coalescence of aerated emulsions was systematically investigated from three fundamental perspectives: fat crystallization, air-liquid interface rheology, and fat globule interface properties. The optimized crystallization of long carbon chain length diacylglycerol (LCD) based on stearate enhances interactions between fat globules at the air-liquid interface (with an elastic modulus E' reaching 246.42 mN/m), leading to a significantly reduced interface membrane strength. This promotes fat crystal-membrane interactions during whipping, resulting in a thermally stable foam structure with excellent shaping capability due to enhanced partial coalescence of fat globules. Although Laurate based medium carbon chain length diacylglycerol (MCD) promoted fat crystallization and optimized interface properties, it showed weaker foam properties because it did not adequately encapsulate air bubbles during whipping. Conversely, oleate long carbon chain length diacylglycerol (OCD) proved to be ineffective in facilitating fat crystal-membrane interaction, causing foam to have a subpar appearance. Hence, drawing from the carefully examined fat crystal-membrane interaction findings, a proposed mechanism sheds light on how DAGs impact the whipping abilities of aerated emulsions. This mechanism serves as a blueprint for creating aerated emulsions with superior whipping capabilities and foam systems that are resistant to heat.

Atomically Engineered Encapsulation of SnS2 Nanoribbons by Single-Walled Carbon Nanotubes for High-Efficiency Lithium Storage.

Rechargeable lithium-ion batteries are integral to contemporary energy storage, yet current anode material systems struggle to meet the increasing demand for extended range capabilities. This work introduces a novel composite anode material composed of one-dimensional 2H-phase tin disulfide (SnS2) nanoribbons enclosed within cavities of single-walled carbon nanotubes (SnS2@SWCNTs), achieved through precise atomic engineering. Employing aberration-corrected transmission electron microscopy, we precisely elucidated the crystal structure of SnS2 within the confines of the SWCNTs. This deliberate design effectively addresses the inherent limitations of SnS2 as a lithium-ion anode material, including its low electrical conductivity, considerable volume expansion effects, and unstable solid electrolyte interface membrane. Testing confirmed that SnS2 transforms into the Li5Sn2 alloy phase after full lithiation and back to SnS2 after delithiation, showing excellent reversibility. The composite also benefits from edge effects, improving lithium storage through stronger binding and lower migration barriers, which were supported by calculations. This pioneering work advances high-performance anode materials for applications.

In vitro mRNA-S maternal vaccination induced altered immune regulation at the maternal-fetal interface.

Maternal-fetal immunology is intricate, and the effects of mRNA-S maternal vaccination on immune regulation at the maternal-fetal interface require further investigation. Our study endeavors to elucidate these immunological changes, enhancing our comprehension of maternal and fetal health outcomes. By analyzing immune profiles and cytokine responses, we aim to provide valuable insights into the impact of mRNA-S vaccination on the delicate balance of immune regulation during pregnancy, addressing critical questions in the field of reproductive pharmacology. This investigation sought to examine the prospective influence of mRNA-S-based vaccines and extracellular vesicles (EVs) containing the Spike (S) protein at the maternal-fetal interface. Our primary emphasis was on evaluating their effects on maternal decidua cells and fetal chorion trophoblast cells (hFM-CTCs). We validated the generation of EVs containing the S protein from small human airway epithelial cell lines (HSAECs) following mRNA-S vaccine exposure. We assessed the expression of angiotensin-converting enzyme 2 (ACE2) gene and protein in fetal membranes and the placenta, with specific attention to decidual cells and fetal membrane chorion cells. To assess cellular functionality, these cells were exposed to both recombinant S protein and EVs loaded with S proteins (eSPs). Our findings revealed that cells and EVs subjected to mRNA-S-based vaccination exhibited altered protein expression levels of S proteins. At the feto-maternal interface, both placental and fetal membrane tissues demonstrated similar ACE-2 expression levels. Among individual cellular layers, syncytiotrophoblast cells in the placenta and chorion cells in the fetal membrane exhibited elevated ACE-2 expression. Notably, EVs derived from HSAECs activated the MAPK pathway in decidual cells. Additionally, decidual cells displayed a substantial increase in gene expression of chemokines like CXCL-10 and CXCL-11, as well as proinflammatory cytokines such as IL-6 in response to eSPs. However, the levels of Ccl-2 and IL-1β remained unchanged in decidual cells under the same conditions. Conversely, hFM-CTCs demonstrated significant alterations in the proinflammatory cytokines and chemokines with respect to eSPs. In conclusion, our study indicates that mRNA-S-based maternal vaccination during pregnancy may influence the maternal-fetal interface's COVID-19 interaction and immune regulation. Further investigation is warranted to assess safety and implications.

Accurate Calculation of Solid-State Li+ Diffusion Coefficient and Kinetic Activation Energies for an Artificial Graphite Anode

The slow electrochemical reaction kinetics of artificial graphite is one of the limiting factors for safety of lithium-ion batteries, especially the lack of systematic research on activation energies of various kinetic processes. In this work, cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic intermittent titration technique (GITT) were used to investigate key kinetic parameters of artificial graphite such as solid-state Li+ diffusion coefficient (D Li+) and activation energy. The results reveal the evaluation of the chemical diffusion coefficient of same material is independent of the technique and shows a similar value, with D Li+ ranging from 10−11 to 10−13 cm2·s−1. The activation energies measured by EIS and GITT for solid-state Li+ diffusion in graphite at 50% depth of discharge are 74.5 kJ·mol−1 and 66.8 kJ·mol−1, which are in the same order of magnitude as the activation energies of charge transfer resistance (59.5 kJ·mol−1), electrode/electrolyte interface membrane impedance (56.1 kJ·mol−1), and ohmic impedance (6.6 kJ·mol−1). It demonstrates that the solid-state Li+ diffusion, interface charge transfer process, and Li+ transmission through SEI membrane are significantly affected by temperature. This work provides a reliable parameter basis for establishing more accurate thermal-electrochemical coupling models and designing safer battery thermal management systems for lithium-ion batteries.

Durable CO2 conversion in the proton-exchange membrane system.

Electrolysis that reduces carbon dioxide (CO2) to useful chemicals can, in principle, contribute to a more sustainable and carbon-neutral future1-6. However, it remains challenging to develop this into a robust process because efficient conversion typically requires alkaline conditions in which CO2 precipitates as carbonate, and this limits carbon utilization and the stability of the system7-12. Strategies such as physical washing, pulsed operation and theuse of dipolar membranes can partially alleviate these problems but do not fully resolve them11,13-15. CO2 electrolysis in acid electrolyte, where carbonate does not form, has therefore been explored as an ultimately more workable solution16-18. Herein we develop a proton-exchange membrane system that reduces CO2 to formic acid at a catalyst that is derived from waste lead-acid batteries and in which a lattice carbon activation mechanism contributes. When coupling CO2 reduction with hydrogen oxidation, formic acid is produced with over 93% Faradaic efficiency. The system is compatible with start-up/shut-down processes, achieves nearly 91% single-pass conversion efficiency for CO2 at a current density of 600 mA cm-2 and cell voltage of 2.2 V and is shown to operate continuously for more than 5,200 h. We expect that this exceptional performance, enabled by the use of a robust and efficient catalyst, stable three-phase interface and durable membrane, will help advance the development of carbon-neutral technologies.

Synergistic effect of egg white protein particles and rhamnolipid on improving the bioavailability of curcumin carried in high internal phase emulsions

SummaryHigh internal phase emulsions (HIPEs) are potential carriers of fat‐soluble nutrients due to their high loading capacity. In this study, egg white protein particles (EWPP) and rhamnolipid (Rha) were used to co‐emulsify oil/water HIPEs to carry curcumin (Cur). The results showed that the Cur loading efficiency, microstructure, protein composition, molecular distribution of protein hydrolysates, protein interfacial adsorption rate and Cur bioavailability were measured. The results showed that, incorporation with Rha was unhelpful for improving loading efficiency of Cur, which decreased from 80.8% to 73.7% at pH 3.8 after incorporation with Rha, due to the decreased viscosity and destroyed continuous interface membrane, while beneficial for restricting coalescence of oil droplets. As studied, Rha could effectively reduce the droplet size to slow down the speed of coalescence and form EWPP–Rha complex to inhibit proteolysis. Finally, Cur bioavailability in EWPP–Rha co‐emulsified HIPE was the highest (40.3%), indicating the synergistic effect of EWPP and Rha promoting the effective adsorption of Cur, related to the increased coalescence stability during digestion and participation of Rha in the micellisation reaction. In comparison, fibrous (pH 3.8) and granular (pH 7.0) EWPP stabilised HIPEs, showed no obvious difference in Cur bioavailability, due to the balance between the interfacial adsorption ability and the digestion resistance of EWPP with various morphologies. This study has important significance for the construction of lipid soluble nutrient ‘carriers’ with high load and high bioavailability.

Influence of lipid vesicle properties on the function of conjugation dependent membrane active peptides.

Membrane active peptides (MAPs) can provide novel means to trigger the release of liposome encapsulated drugs to improve the efficacy of liposomal drug delivery systems. Design of MAP-based release strategies requires possibilities to carefully tailor the interactions between the peptides and the lipid bilayer. Here we explore the influence of lipid vesicle properties on the function of conjugation-dependent MAPs, specifically focusing on two de novo designed peptides, JR2KC and CKV4. Utilizing liposomes with differences in size, lipid composition, and surface charge, we investigated the mechanisms and abilities of the peptides to induce controlled release of encapsulated cargo. Our findings indicate that liposome size modestly affects the structural changes and function of the peptides, with larger vesicles facilitating a minor increase in drug release efficiency due to higher peptide-to-liposome ratios. Notably, the introduction of negatively charged lipids significantly enhanced the release efficiency, predominantly through electrostatic interactions that favor peptide accumulation at the lipid bilayer interface and subsequent membrane disruption. The incorporation of cholesterol and a mix of saturated and unsaturated lipids was shown to alter the vesicle's phase behavior, thus modulating the membrane activity of the peptides. This was particularly evident in the cholesterol-enriched liposomes, where JR2KC induced lipid phase separation, markedly enhancing cargo release. Our results underscore the critical role of lipid vesicle composition in the design of MAP-based drug delivery systems, suggesting that precise tuning of lipid characteristics can significantly influence their performance.

Degradation Issues in Solid Oxide Electrolysers

One of the crucial aspects to achieving long lifetime and high-efficient SOCs (Solid oxide cells) is to enhance durability of the current devices.Degradation issues are typically associated with problems in both electrodes. For example, nickel-yttria stabilized zirconia (Ni-YSZ) hydrogen electrodes present under extreme conditions of high steam partial pressures, a low durability due to Ni oxidation resulting in lowered electronic conductivity and catalytic activity of the electrode. Ni agglomeration, depleting and micro crack in Ni-containing hydrogen electrode can also occur leading to a lower activity of the Ni-based electrodes as an SOEC fuel electrode. Furthermore, carbon deposition and sulfur poisoning on the Ni surface are also lead to cell performance degradation and poor durability.In addition, the performance of the oxygen electrode is also particularly more important in electrolysis mode than in fuel cell mode, as it is well established that electrochemically induced oxygen pressure increase at the electrolyte-oxygen electrode interface and subsequent membrane failure have been theoretically predicted and experimentally observed in SOEC mode. For example, several examples in the literature reported the presence on voids at the YSZ electrolyte, leading to delamination of the oxygen electrode. In this sense, lanthanide nickelates (Ln = La, Nd, Pr) have received considerable interest as materials for IT-SOFC electrodes and oxygen separation membranes, and they seem to be very attractive for electrolysis applications. The hyperstoichiometry of some oxygen electrode materials such as these Ruddlesden-Popper phases is believed to be favourable for effective oxygen evolution, as performance of these electrodes is enhanced in SOEC mode.Different strategies to develop optimized electrode structures as well as controlled operating conditions will be discussed in order to improve the durability of SOCs.

Thermal Stability Improvement of Core Material via High Internal Phase Emulsion Gels.

Biocompatible particle-stabilized emulsions have gained significant attention in the biomedical industry. In this study, we employed dynamic high-pressure microfluidization (HPM) to prepare a biocompatible particle emulsion, which effectively enhances the thermal stability of core materials without the addition of any chemical additives. The results demonstrate that the HPM-treated particle-stabilized emulsion forms an interface membrane with high expansion and viscoelastic properties, thus preventing core material agglomeration at elevated temperatures. Furthermore, the particle concentration used for constructing the emulsion gel network significantly impacts the overall strength and stability of the material while possessing the ability to inhibit oxidation of the thermosensitive core material. This investigation explores the influence of particle concentration on the stability of particle-stabilized emulsion gels, thereby providing valuable insights for the design, improvement, and practical applications of innovative clean label emulsions, particularly in the embedding and delivery of thermosensitive core materials.

Unexpected positive cultures in patients with arthrofibrosis following total hip and total knee arthroplasty.

It has been suggested that low-grade infections could be the cause of arthrofibrosis. However, this hypothesis has not been conclusively proven. The aim of this study is to assess the incidence of unexpected positive cultures (UPC) in patients undergoing revision total joint arthroplasty for a diagnosis of arthrofibrosis. A retrospective single-centre review was performed. All patients who underwent an aseptic revision due to histologically confirmed arthrofibrosis (based on the synovial-like interface membrane (SLIM) criteria) were included. The incidence of UPC was then calculated. A total of 147 patients were included. Of these, 100 underwent a total knee arthroplasty (TKA) procedure and 46 a total hip arthroplasty (THA) surgery. One patient had a periprosthetic joint infection and was therefore excluded. Of the 146 included patients, 6 had confirmed UPC (4.08%). The following bacteria were identified: Anaerococcus octavius, Staphylococcus epidermidis, Enterobacter cloacae, Staphylococcus hominis, Streptococcus pluranimalium, Staphylococcus pettenkoferi. Our results suggest that the incidence of UPC in patients with arthrofibrosis is low. It is lower than that of UPC in patients that undergo a revision for other causes. There is no proven relationship between histologically confirmed arthrofibrosis following total joint arthroplasty and prosthetic joint infection.

Facile decoration of fluorinated metal–organic frameworks on copper foil for regulated lithium deposition and robust solid electrolyte interface

Lithium metal is one of the most promising anode materials for Li-ion batteries. However, lithium metal anodes suffer from low coulomb efficiency, short cycle life, and even serious safety issues, owing to the incompatible Cu/Li interface and brittle solid electrolyte interface (SEI). A facile strategy is proposed to construct stable lithium metal anodes by regulating both the Cu/Li interface and SEI membrane with a thin layer of copper-tetrafluoroterephthalate (CuTFBDC), which can guide the uniform lithium deposition and the LiF-rich SEI. The prepared CuTFBDC@Cu foils can be applied as current collectors, and the assembled Li@CuTFBDC@Cu//Li symmetric cell exhibits a stable performance at a current density of 0.5 mA cm−2 for more than 3000 h, with a small voltage hysteresis of less than 11.5 mV, surpassing that of the bare Cu foil. The assembled Li@CuTFBDC@Cu//LFP (LiFePO4) full cell proceeds smoothly for 200 cycles at a current density of 2 C with a specific capacity of 133.8 mAh/g, and the capacity can be maintained at 125.29 mAh/g after 250 cycles. This facile strategy can provide a solution for both the Cu/Li interface and SEI membrane, showing an excellent prospect for practical applications in lithium metal batteries.

Effect of nonionic surfactants on the synergistic interaction between asphaltene and resin: Emulsion phase inversion and stability

Interaction between surface active components in crude oils and nonionic surfactants plays an important role in phase inversion behavior of crude oil emulsion, while the interaction mechanism is not yet fully explored. Herein, the effects of nonionic surfactants on the synergistic interaction between asphaltene and resin, emulsion stability, and emulsion phase inversion were investigated. It is shown that the addition of Span 80 and Tween 80 promotes the reduction of phase inversion point of water in oil emulsion stabilized by asphaltene and resin, as well as increases the yield strain value of the emulsion. The addition of Tween 80 to the asphaltene and resin mixture reduces the inversion point from 70 % to 30 %. The decrease of phase inversion point is attributed to the difficulty in the formation of multiple emulsions after adding nonionic surfactants. The addition of nonionic surfactants can affect the hydrogen bonding between asphaltene and resin, thereby improving the emulsion stability. Span 80 coexists with asphaltene and resin at oil-water interface, reducing the Turbiscan Stability Index (TSI) of emulsion by 15 and improving the strength of the oil-water interface membrane. In comparison, Tween 80 with stronger hydrophilic ability dissolves asphaltene and resin into bulk phase, which leads to the oil-water interface occupied by a large amount of Tween 80. Its numerous EO groups result in the strong hydrogen bonding on the oil-water interface membrane, effectively increasing the strength of the oil-water interface membrane and reducing the TSI by 19. This work contributes to a better understanding of the phase inversion of crude oil emulsion and improves crude oil recovery.

Interfacial Proton Supply/Filtration Regulates the Dynamics of Electrocatalytic Nitrogen Reduction Reaction: A Perspective

AbstractAs a promising energy carrier, ammonia synthesis by electrocatalytic nitrogen reduction reaction (eNRR) is a promising green and low‐carbon ammonia synthesis strategy that can replace the traditional Haber–Bosch process. However, the development of eNRR processes is mainly severely constrained by competitive hydrogen evolution reaction (HER), and the corresponding strategies to inhibit this adverse side reaction to obtain high eNRR selectivity are still limited. In addition, for this complex reaction involving gas–liquid–solid three‐phase interface and proton/electron transfer, it is great significance to analyze and summarize the existing inhibition HER strategies from the viewpoint of dynamics. In view of this, this work reviews proton supply/filtration regulation strategy in catalytic system, allowing a systematic survey of the literature focusing on interface membrane regulation (inorganic membrane and organic membrane), electrolyte regulation (metal‐mediated strategy and electrolyte ion regulation strategy) and system device design (electrode structure design and electrolytic cell device design). Constructive catalytic system design guidance is also suggested to inhibit hydrogen evolution and improve NH3 selectivity, aiming for scalable and economically feasible applications.

Key role of three-dimensional reticular interface membranes in the formation of single polysaccharide–stabilized high internal phase emulsions

Although the interfacial activity of polysaccharides is believed to be insufficient for their applications as individual emulsifying stabilizers, four single polysaccharides examined herein, namely sodium carboxymethyl cellulose (Na-CMC), sodium alginate (SA), high-methoxyl pectin (HMP), and low-methoxyl pectin (LMP) are shown to effectively stabilize high internal phase emulsions (HIPEs) at loadings as low as 0.1 wt% under acidic conditions, that is, at pH 0.5–5.2 (Na-CMC), 0.5–4.0 (SA), 1.0–4.2 (HMP), and 1.0–3.0 (LMP). Despite their structural differences, the four studied polysaccharides feature similar HIPE stabilization mechanisms that mainly involve the formation of three-dimensional reticular interface membrane structures with fiber branching chains. Within the pH range suitable for HIPE formation, the polysaccharides mainly exist as nanofiber network structures with a grid width of 50–100 nm but adopt flake-like and other structures at higher pH. Further insights are provided by the relationship between network membrane structures formed at the interface and the fiber network structures formed by polysaccharides in the original aqueous phase. In addition, the inferred emulsification and stabilization mechanisms are shown to be significantly different from those observed for mainstream Pickering HIPE stabilizers. Thus, our work expands the understanding of the interfacial activity function of polysaccharides, provides conceptual thinking reference and design rules for the development of simple, efficient, safe, and cheap polysaccharide-based HIPEs, and supplements and furthers the theory of HIPE stabilization.

Bone and Soft Tissue Reaction to Co(II)/Cr(III) Ions Stimulation in a Murine Calvaria Model: A Pioneering in vivo Study.

Metal ions released during wear and corrosion of the artificial knee/hip joints are considered to contribute to aseptic implant failure. However, there are few convincing in vivo studies that demonstrate the effects of metal ions on bone and soft tissue. This study examined the in vivo effects of Co(II)/Cr(III) ions on mouse calvaria and the supra-calvaria soft tissue in an original mouse model. With the implantation of a helmet-like structure, we set up a subcutaneous cavity on the calvaria in which Co(II) Chloride or Cr(III) Chloride solutions were administered respectively. A layer of interface membrane formed on the calvaria along with the implantation of the helmet. The administered Cr(III) ions accumulated in the interface membranes while Co(II) disseminated into the circulation. Accumulated Cr(III) and related products induced local massive macrophage infiltration and skewed the bone metabolic balance. At last, we revealed that lymphocyte aggregates, which are the pathologic hallmark of human periprosthetic tissue, could be caused by either Co(II) or Cr(III) stimulation. These in vivo results may shed light on the effects and pathogenic mechanism of the Co(II)/Cr(III) ions released from the joint prosthesis. STATEMENT OF SIGNIFICANCE: Macrophage infiltration and lymphocyte aggregates are hallmarks of human joint periprosthetic tissue. We chronically administered Co(II)/Cr(III) ions on mouse calvaria and reproduced these two histopathologic hallmarks on mouse tissue based on an implanted helmet-like structure. Our results reveal that Cr(III) ions are locally accumulated and are effective in inducing macrophage infiltration and they can be phagocytosed and stored. However, the lymphocytes aggregates could be induced by both Co(II), Cr(III) and other unspecific inflammatory stimuli.

Rab7/Retromer-based endolysosomal trafficking is essential for proper host invasion in rice blast.

Secretion is a fundamental process that plant pathogens utilize to deliver effectors into the host to downregulate immunity and promote infection. Here, we uncover a fascinating membrane trafficking and delivery route that originates from vacuolar membranes in Magnaporthe oryzae and conduits to the host interface and plasma membrane. To perform such secretory/trafficking function, MoRab7 first recruits the retromer complex to the vacuolar membrane, enabling recognition of a family of SNARE proteins, including MoSnc1. Live-cell imaging confirmed a highly dynamic vesicular trafficking of the retromer complex component(s) and MoSnc1 toward and across the host interface or plasma membrane, and subsequent fusion with target membranes. Interestingly, disruption of the MoRab7/Retromer/MoSnc1-based endolysosomal cascade affects effector secretion and fungal pathogenicity. Taken together, we discovered an unconventional protein and membrane trafficking route starting from the fungal endolysosomes to the M. oryzae-rice interaction interface and dissect the role of MoRab7/Retromer/MoSnc1 sorting machinery in effector secretion during biotrophy and invasive growth in rice blast fungus.