Improving paste stabilities of cassava starch through molecular density after maltogenic amylase and transglucosidase.

To improve paste stability of cassava starch, including acid resistance, high-temperature shear resistance and freeze-thaw stability, cassava starch was modified by sequential maltogenic amylase and transglucosidase to form an optimally denser structure, or branched density (12.76 %), molecular density (15.17 g/mol/nm3), and the proportions of short-branched chains (41.41 % of A chains and 44.01 % of B1 chains). Viscosity stability (88.52 %) of modified starch was higher than that (64.92 %) of native starch. After acidic treatment for 1 h, the viscosity of modified starch and native starch decreased by 56.53 % and 65.70 %, respectively. Compared to native starch, modified starch had lower water loss in freeze-thaw cycles and less viscosity reduction during high-temperature and high-shear processing. So, the appropriate molecular density and denser molecule structure enhanced paste stabilities of modified starch. The outcome expands the food and non-food applications of cassava starch.

A preclinical model for osteoarticular fracture fragment preservation for delayed re-implantation.

Background: Open articular fractures often include contaminated, devascularized osteoarticular fragments that are critical for joint reconstruction. Definitive treatment is often delayed such that decontamination and preservation of critical fragments for joint reconstruction is highly desirable. To validate decontamination and preservation protocols for safe and effective preservation of osteoarticular fragments for re-implantation, a preclinical animal model for inducing type 3 open articular fractures with contaminated, devascularized osteoarticular fragments was developed and validated. Materials and methods: With IACUC approval, purpose-bred hounds (n = 5) were humanely euthanized. Immediately following euthanasia, a penetrating captive bolt pistol with 1.25 grain cartridge centered on the cranial aspect of each distal humerus was discharged to create open fractures in 3 dogs (6 elbows). In 2 dogs, matched osteoarticular tissues from non-injured elbows (controls) were retrieved for comparison. Distal humerus, proximal radius, and proximal ulna osteoarticular fragments (n = 27) were immediately placed in Missouri Osteochondral Preservation System (MOPS) solution and stored at room temperature. Radiographic, chondrocyte viability, and quantitative microbial culture assessments were performed immediately (time-0) and at 7 and 14 days of storage. Results: This preclinical canine model reliably produced type 3 open distal humeral fractures characterized by devascularized and contaminated osteoarticular fracture fragments. All fragments produced extensive microbial growth through 14 days of storage. Without decontamination, viable chondrocyte density in the fragments decreased significantly within 7 days, likely attributable to the profound contamination. Conclusion: These data highlight the importance of developing a reliable method for point-of-care decontamination and preservation of osteoarticular fracture fragments for safe and effective reimplantation of articular fracture fragments for joint reconstruction.

Enhanced Fenton-like reactions via interface electron reconstruction in low-crystallinity FeCo bimetallic metal-organic frameworks: Bidirectional control of Fe (III) and Co (II) sites.

In this study, the activity and stability of Fenton-like reactions are enhanced by constructing a low-crystallinity FeCo bimetallic metal-organic framework (FeCox-BDC (BDC denotes as terephthalic acid)) through interface electron reconstruction. However, the specific origins and mechanisms of their enhanced activity, particularly in Fenton-like reactions, remains unclear. Systematic analysis revealed that the isomorphic substitution of Co (II) reduces the coordination number and d-electron count at local Fe (III) sites, shifting the d-band centers (-1.59 eV) closer to the Fermi level. Additionally, Co 3d-orbitals can accept electrons, improving the occupation of antibonding orbitals. Notably, Fe (III) and Co (II) sites exhibit a synergistic effect: Fe (III) sites strongly adsorbed the Oα point of the peroxy bond (lOαOß), while Co (II) sites efficiently activated Oß. Within 5 min, FeCo1/3-BDC achieved a 98 % reduction in Rhodamine-B (RhB), surpassing Fe-BDC by a factor of 76 and homogeneous Fenton catalytic systems (Co (II)/peroxymonosulfate (PMS) and Fe (III)/Co (II)/PMS). This work provides a profound understanding of interface electron reconstruction, offering valuable insights into guiding Fenton-like mechanisms.

Dual cross-linked magnetic gelatin/carboxymethyl cellulose cryogels for enhanced Congo red adsorption: Experimental studies and machine learning modelling.

To achieve highly efficient and environmentally degradable adsorbents for Congo red (CR) removal, we synthesized a dual-network nanocomposite cryogel composed of gelatin/carboxymethyl cellulose, loaded with Fe3O4 nanoparticles. Gelatin and sodium carboxymethylcellulose were cross-linked using transglutaminase and calcium chloride, respectively. The cross-linking process enhanced the thermal stability of the composite cryogels. The CR adsorption process exhibited a better fit to the pseudo-second-order model and Langmuir model, with maximum adsorption capacity of 698.19 mg/g at pH of 7, temperature of 318 K, and initial CR concentration of 500 mg/L. Thermodynamic results indicated that the CR adsorption process was both spontaneous and endothermic. The performance of machine learning model showed that the Extreme Gradient Boosting model had the highest test determination coefficient (R2 = 0.9862) and the lowest root mean square error (RMSE = 10.3901 mg/g) among the 6 models. Feature importance analysis using SHapley Additive exPlanations (SHAP) revealed that the initial concentration had the greatest influence on the model's prediction of adsorption capacity. Density functional theory calculations indicated that there were active sites on the CR molecule that can undergo electrostatic interactions with the adsorbent. Thus, the synthesized cryogels demonstrate promising potential as adsorbents for dye removal from wastewater.

Enhanced electrochemical stability and ion transfer rate: A polymer/ceramic composite electrolyte for high-performance all-solid-state lithium-sulfur batteries.

All-solid-state (ASS) lithium-sulfur (LiS) batteries utilizing composite polymer electrolytes (CPEs) represent a promising avenue in the domain of electric vehicles and large-scale energy storage systems, leveraging the combined benefits of polymer electrolytes (PEs) and ceramic electrolytes (CEs). However, the inherent weak interface compatibility between PEs and CEs often leads to phase separation, thereby impeding the transposition of Li+. In this study, the trimethoxy-[3-(2-methoxyethoxy)propyl]silane (TM-MES) is introduced as a chemical agent to form bonds with polyethylene oxide (PEO) and Li10GeP2S12 (LGPS), resulting in the development of a novel composite polymer electrolyte (CPETM-MES). This innovative approach mitigates phase separation between PEs and CEs while concurrently enhancing the protective capabilities of LGPS against decomposition at the interfaces of both the Li anode and sulfur cathode. Moreover, the CPETM-MES exhibits superior mechanical toughness, an expanded electrochemical window, and elevated ionic conductivity. In the symmetric cell, it demonstrates an extended operational lifespan exceeding 1800 h, and the current density can reach up to 1.05 mA/cm2. Furthermore, the initial discharge capacity of ASS LiS batteries utilizing CPETM-MES attains 1227 mAh/g and maintains a capacity of 904 mAh/g after 100 cycles. Notably, a high-energy-density of 2454 Wh/kg is achieved based on the sulfur cathode.

Nitrogen plasma-induced phase engineering and titanium carbide/carbon nanotubes dual conductive skeletons endow molybdenum disulfide with significantly improved lithium storage performance.

MoS2/Ti3C2 MXene composite has emerged as a promising anode material for lithium storage due to the synergistic combination of high specific capacity offered by MoS2 and conductive skeleton provided by Ti3C2 MXene. However, its two-dimensional/two-dimensional (2D/2D) structure is susceptible to collapse after long cycles, while the inherent low conductivity of MoS2 limits its rate performance. In this study, we developed a novel approach combining plasma-induced phase engineering with dual skeleton structure design to fabricate a unique P-MoS2/Ti3C2/CNTs anode material featuring highly conductive 1T phase MoS2 and a stable one-dimensional/two-dimensional (1D/2D) architecture. Within this architecture, growth of MoS2 nanosheets on the surface of Ti3C2 cross-linked by carbon nanotubes (CNTs) was achieved. The resulting Ti3C2/CNTs dual skeleton not only provides robust mechanical support to prevent structural collapse during long cycles but also offers increased specific surface area and additional Li+ storage space, thereby enhancing the lithium storage capacity of the composite. Subsequent N2 plasma treatment induced a phase transition in MoS2 from 2H to 1T configuration. Density functional theory (DFT) calculations confirmed that the induced 1T-MoS2 exhibits higher conductivity and lower Li+ diffusion barrier compared to 2H-MoS2. Benefiting from these synergistic effects, our P-MoS2/Ti3C2/CNTs anode demonstrated remarkable electrochemical performance including a high reversible specific capacity of 1120 mAh g-1 at 0.1 A g-1, excellent cycling stability with a specific capacity retention of 670 mAh g-1 after 600 cycles at 1 A/g, and superior rate performance with a specific capacity of 614 mAh g-1 at 2 A g-1. This combined modification strategy will serve as guidance for designing other energy storage materials.

Partially amorphous NiFe layered double hydroxides enabling highly-efficiency oxygen evolution reaction at high current density.

Layered double hydroxide (LDH) serves as an innovative catalyst for water electrolysis, showcasing outstanding performance in the oxygen evolution reaction (OER) under alkaline conditions. However, it faces challenges due to its low electrical conductivity and limited accessibility to active sites. In this work, the flexibility advantages of disordered amorphous and ordered crystals in NiFe LDH were combined to improve OER performance and maintain long-term stability. This combination induces a variety of effects, including improving the intrinsic activity, changing the OER mechanism from adsorb evolution mechanism (AEM) to lattice oxygen mechanism (LOM), and promoting the reaction kinetics of the catalyst. Moreover, the porous structure of NiFe LDH can efficiently alleviate the issue of local acidic environment induced by prolonged OER reaction, satisfying the criteria for long-term stability. Therefore, the NiFe-2.0 LDH catalyst only requires an ultralow overpotential of 189 mV at a current density of 10 mA cm-2 with Tafel slope of 43 mV dec-1. More importantly, the catalyst not only displays excellent electrocatalytic activity with an overpotential of 289 mV but also represents an outstanding stability over 80 h at an ultra-high current density of 1 A cm-2. This study provides a promising strategy for optimizing the catalytic activity and stability of catalyst at ampere current density, which is expected to achieve commercial applications.

CrSe2 based single-cluster catalysts with controllable charge states for the oxygen reduction and hydrogen evolution reactions.

Development of affordable catalysts for the oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER) represents a central task for advancing electrochemical systems such as fuel cells and metal-air batteries. This study reported the ORR and HER performance of a set of single cluster catalysts (SCCs) with atomically dispersed 3d/4d/5d transition metal cluster (TM3) embedded in a two-dimensional (2D) defective CrSe2 substrate. Distinguishing from the conventional SCCs with positive charge active center, the unique electronegativity discrepancy between the metal clusters and the substrate renders the active center controllable charge states from negative to positive. Our investigations indicate that the TM3 cluster helps tuning the adsorption performance of the intermediates, and therefore enhancing the electrocatalytic activity of the SCCs. Among all the candidates, we demonstrated that the less reported elements of Ir and Ag exhibit the best performance of HER and ORR with low overpotentials of -0.059 and 0.61 V, respectively. Our work provides a prototype to rationally regulate the charge states of catalysts, which could potentially contribute to the development of new kinds of catalysts and serve as a valuable theoretical reference for the experimental rationalization of SCCs.

Core-shell structured MgCo2O4@Ni(OH)2 nanorods as electrode materials for high-performance asymmetric supercapacitors.

In the field of energy storage, supercapacitors have received extensive attention in recent years. However, achieving the expected electrochemical performance and energy density of supercapacitors is still a huge challenge. The design and synthesis of binder-free composite electrode with core-shell structure is an effective strategy to improve the electrochemical performance of supercapacitors. In this paper, a heterogeneous core-shell structured and binder-free electrode material MgCo2O4@Ni(OH)2 (MCO@NH) grown on nickel foam (NF) is prepared by a simple hydrothermal and oil bath method. The unique core-shell structure makes the MCO@NH have a large specific surface area, which provides abundant active sites for ion transport and storage, thereby improving the electrochemical performance. The MCO@NH/NF nanocomposite demonstrates a high specific capacitance (Cs) of 1583 F g-1 at 1 A/g. A solid-state asymmetric supercapacitor (ASC) assembled with MCO@NH/NF and active carbon (AC) exhibits excellent energy density (45 Wh kg-1 at 457.5 W kg-1) and outstanding capacitance (89.51 %) and coulombic efficiency (97.8 %) after 12,000 cycles, evidencing its good operation stability and potential practical applications. Therefore, the prepared core-shell MCO@NH/NF electrode can be a promising candidate for energy storage devices.

Interfacial engineering of ruthenium-nickel for efficient hydrogen electrocatalysis in alkaline medium.

Developing highly efficient electrocatalyst with heterostructure for hydrogen evolution and oxidation reactions (HER/HOR) in alkaline media is crucial to the fabrication and conversion of hydrogen energy but also remains a great challenge. Herein, the synthesis of ruthenium-nickel nanoparticles (Ru3-Ni NPs) with heterostructure for hydrogen electrocatalysis is reported, and studies show that their catalytic activity is improved by electron redistribution caused by the distinctly heterogeneous interface. Impressively, Ru3-Ni NPs possess the remarkable exchange current density (2.22 mA cm-2) for HOR. Additionally, an ultra-low overpotential of 28 mV is required to attain a current density of 10 mA cm-2 and superior stability of 200 h for HER. The highly efficient catalytic activity can be attributed to the electron transfer from Ni to Ru and the optimal adsorption of H* on Ru-Ni sites. Our study showcases a reliable heterostructure that boosts the HOR/HER activity of the catalyst in alkaline environments. This work provides a new pathway for designing high-performance electrocatalyst for energy storage and conversion.

Enhanced charge storage in supercapacitors using carbon nanotubes and N-doped graphene quantum dots-modified (NiMn)Co2O4.

The integration of ternary metal oxides into carbon materials is anticipated to significantly boost the electrochemical performance of supercapacitor electrodes. This article synthesized carbon nanotubes (CNT)/(NiMn)Co2O4 composite materials using a straightforward hydrothermal method and subsequently prepared composite thin films of CNT/P-(NiMn)Co2O4@NGQD by phosphating and incorporating nitrogen-doped graphene quantum dots (NGQD). These films served as the functional electrode material for supercapacitors, enhancing their performance capabilities. The specific capacity of CNT/P-(NiMn)Co2O4@NGQD was measured at 2172.0 F g-1 at a current density of 1 A g-1, maintaining a capacitance of 1954.0 F g-1 at 10 A g-1, thus demonstrating excellent rate performance. Electrochemical impedance spectroscopy (EIS) further revealed enhancements in electrolyte flow dynamics and capacitance behavior post-NGQD introduction. The energy density of the composite material reached 94.4 Wh kg-1 at power density of 800 W kg-1, demonstrating superior electrochemical performance. The enhancement in these electrochemical properties is attributed to the high specific surface area and active sites of CNT/P-(NiMn)Co2O4@NGQD films, along with the synergistic effects of NGQD and metal ions facilitating rapid electrons and charge transfer. This work provides new insights into developing high-performance supercapacitors.

Vacancy-rich heterogeneous MnCo2O4.5@NiS electrocatalyst for highly efficient overall water splitting.

Alkaline water electrolysis is regarded as a promising technology for sustainable energy conversion. Spinel oxides have attracted considerable attention as potential catalysts because of their diverse metal valence states. However, achieving the required current densities at low voltages is a challenge due to its limited active sites and suboptimal electron transport. In this study, we present a novel bifunctional catalyst composed of MnCo2O4.5 nanoneedles grown on NiS nanosheets for water electrolysis. Remarkably, MnCo2O4.5@NiS demonstrates exceptional catalytic activity, requiring 187 and 288 mV to achieve a current density of 100 mA cm-2 for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively. The impressive performance of MnCo2O4.5@NiS is demonstrated by the lower value of voltage 1.44 V needed to deliver the current density of 10 mA cm-2, which outperformed the 1.66 V required for a commercial Pt/C||RuO2 system. Detailed structure analysis and density functional theory (DFT) calculations reveal that the MnCo2O4.5@NiS heterostructure enhances electron transfer at the interface, promotes the formation of oxygen vacancies and tunes the electronic structures of Mn and Co. These findings underscore the potential of MnCo2O4.5@NiS as an efficient and cost-effective electrocatalyst for hydrogen production.

Unraveling the catalytic performance of RuO2(1 1 0) for highly-selective ethylene production from methane at low temperature: Insights from first-principles and microkinetic simulations.

Despite significant progress in low-temperature methane (CH4) activation, commercial viability, specifically obtaining high yields of C1/C2 products, remains a challenge. High desorption energy (>2 eV) and overoxidation of the target products are key limitations in CH4 utilization. Herein, we employ first-principles density functional theory (DFT) and microkinetics simulations to investigate the CH4 activation and the feasibility of its conversion to ethylene (C2H4) on the RuO2 (1 1 0) surface. The CH activation and CH4 dehydrogenation processes are thoroughly investigated, with a particular focus on the diffusion of surface intermediates. The results show that the RuO2 (1 1 0) surface exhibits high reactivity in CH4 activation (Ea = 0.60 eV), with CH3 and CH2 are the predominant species, and CH2 being the most mobile intermediate on the surface. Consequently, self-coupling of CH2* species via CC coupling occurs more readily, yielding C2H4, a potential raw material for the chemical industry. More importantly, we demonstrate that the produced C2H4 can easily desorb under mild conditions due to its low desorption energy of 0.97 eV. Microkinetic simulations based on the DFT energetics indicate that CH4 activation can occur at temperatures below 200 K, and C2H4 can be desorbed at room temperature. Further, the selectivity analysis predicts that C2H4 is the major product at low temperatures (300-450 K) with 100 % selectivity, then competes with formaldehyde at intermediate temperatures in the CH4 conversion over RuO2 (1 1 0) surface. The present findings suggest that the RuO2 (1 1 0) surface is a potential catalyst for facilitating ethylene production under mild conditions.

Modification of metals and ligands in two-dimensional conjugated metal-organic frameworks for CO2 electroreduction: A combined density functional theory and machine learning study.

Electrochemical carbon dioxide reduction reaction (CO2RR) is a promising technology to establish an artificial carbon cycle. Two-dimensional conjugated metal-organic frameworks (2D c-MOFs) with high electrical conductivity have great potential as catalysts. Herein, we designed a range of 2D c-MOFs with different transition metal atoms and organic ligands, TMNxO4-x-HDQ (TM = Cr∼Cu, Mo, Ru∼Ag, W∼Au; x  = 0, 2, 4; HDQ = hexadipyrazinoquinoxaline), and systematically studied their catalytic performance using density functional theory (DFT). Calculation results indicated that all of TMNxO4-x-HDQ structures possess good thermodynamic and electrochemical stability. Notably, among the examined 37 MOFs, 6 catalysts outperformed the Cu(211) surface in terms of catalytic activity and product selectivity. Specifically, NiN4-HDQ emerged as an exceptional electrocatalyst for CO production in CO2RR, yielding a remarkable low limiting potential (UL) of -0.04 V. CuN4-HDQ, NiN2O2-HDQ, and PtN2O2-HDQ also exhibited high activity for HCOOH production, with UL values of -0.27, -0.29, and -0.27 V, respectively, while MnN4-HDQ, and NiO4-HDQ mainly produced CH4 with UL values of -0.58 and -0.24 V, respectively. Furthermore, these 6 catalysts efficiently suppressed the competitive hydrogen evolution reaction. Machine learning (ML) analysis revealed that the key intrinsic factors influencing CO2RR performance of these 2D c-MOFs include electron affinity (EA), electronegativity (χ), the first ionization energy (Ie), p-band center of the coordinated N/O atom (εp), the radius of metal atom (r), and d-band center (εd). Our findings may provide valuable insights for the exploration of highly active and selective CO2RR electrocatalysts.

Constructing nitrogen-doped graphene quantum dots embedded in CNT supported layered (Ni0.5Co0.5)3V2O8 self-supporting film for high-performance supercapacitor.

To improve the electrochemical performance of positive electrode materials, constructing graded nanostructures is a worthwhile approach. This study successfully synthesized nitrogen-doped graphene quantum dots (NGQD) modified (Ni0.5Co0.5)3V2O8 on a carbon nanotube (CNT) substrate to construct self-supporting electrodes for high-performance supercapacitors. The (Ni0.5Co0.5)3V2O8 nanosheets were successfully wrapped onto the CNT surface through a solution impregnation process, which increased the specific surface area and interlayer spacing of the material. Furthermore, the electrochemical properties of the electrode material underwent significant enhancement due to the synergistic interplay between metal ions and the numerous redox centers. The embedding of the NGQD enriched the materials with active sites and further improved its specific capacity without compromising the structure intergrity of the layer configuration. Using CNT as the substrate ensured the self-supporting nature of the electrode. Consequently, the (Ni0.5Co0.5)3V2O8/NGQD@CNT composite exhibits an ultra-high specific capacitance of 3018.2 F g-1 at 1 A g-1 and 2332 F g-1 at 10 A g-1. The asymmetric supercapacitor constructed with (Ni0.5Co0.5)3V2O8/NGQD@CNT and activated carbon (AC) presented an impressive energy density of 160.2 Wh kg-1 at a power density of 800 W kg-1. After 8000 charge-discharge cycles, the capacity retention rate was 78.5 %, with a Coulo mbic efficiency consistently above 98 %.

Optimizing photocatalytic hydrogen evolution performance by rationally constructing S-scheme heterojunction to modulate the D-band center.

The research in the field of photocatalysis has progressed, with the development of heterojunctions being recognized as an effective method to improve carrier separation efficiency in light-induced processes. In this particular study, CuCo2S4 particles were attached to a new cubic CdS surface to create an S-scheme heterojunction, thus successfully addressing this issue. Specifically, owing to the higher conduction band and Fermi level of CuCo2S4 compared to CdS, they serve as the foundation and driving force for the formation of an S-scheme heterojunction. Through in-situ X-ray photoelectron spectroscopy and electron paramagnetic resonance analysis, the direction of charge transfer in the composite photocatalyst under light exposure was determined, confirming the charge transfer mechanism of the S-scheme heterojunction. By effectively constructing the S-scheme heterojunction, the d-band center of the composite photocatalyst was adjusted, reducing the energy needed for electron filling in the anti-bonding energy band, promoting the transfer of photogenerated carriers, and ultimately enhancing the photocatalytic hydrogen production. performance. After optimization, the hydrogen evolution activity of the composite photocatalyst CdS-C/CuCo2S4-3 reached 5818.9 µmol g-1h-1, which is 2.6 times higher than that of cubic CdS (2272.3 µmol g-1h-1) and 327.4 times higher than that of CuCo2S4 (17.8 µmol g-1h-1), showcasing exceptional photocatalytic activity. Electron paramagnetic resonance and in situ X-ray photoelectron spectroscopy have established a theoretical basis for designing and constructing S-scheme heterojunctions, offering a viable method for adjusting the D-band center to enhance the performance of photocatalytic hydrogen evolution.

Exploring PtAg onto silanized biogenic silica as an electrocatalyst for H2 evolution: A combined experimental and theoretical investigation.

The task of creating a remarkably stable and effective electrochemical catalyst for efficient hydrogen evolution is arduous, primarily due to the multitude of factors that need to be taken into account for the industrial utilization of Pt. In this work, hybrid formation through in-situ reduction of Pt onto biogenic porous silica (Pt-SiO2) is tested for its use as an efficient catalyst for hydrogen production. Exceptionally high electrocatalytic activity and excellent reusability of catalysts up to 200 cycles have been demonstrated. Pt-SiO2 with low Pt content of 0.48 to 0.82 at% with active catalytic sites exhibit superior catalytic activity with a Tafel slope of 22 mV dec-1 and an overpotential of 28 mV (vs. RHE at 10 mA cm-2) as compared to the Pt wire and previously reported bare Pt-SiO2 (0.65 at% and 0.48 at% of Pt), and hybrid (Pt/Ag) structures formed onto two different biogenic porous SiO2 substrates. The best catalytic performance of the Pt1Ag3 cluster, representing a low Pt concentration, has been validated by Density Functional Theory (DFT) calculations. Here, the high production from the Pt1Ag3 cluster is assigned to the mutual synergistic effect between Pt/Ag atoms. The Pt atoms transfer the excess charge to the nearest Ag neighbors inside the cluster, facilitating hydrogen diffusion on the activated sites. These important findings authenticate the superior hydrogen production at reduced Pt concentration on amine-functionalized biogenic porous silica.

γδ T-Cell Immunophenotype for the Study of Human Aging.

Flow cytometry serves as a crucial tool in immunology, allowing for the detailed analysis of immune cell populations. γδ T cells, a subset of T cells, play pivotal roles in immune surveillance and immune aging. Assessing the phenotype and functional capabilities of γδ T cells isolated from whole blood or tissue within the context of human aging yields invaluable insights into the dynamic changes affecting immune function, tissue homeostasis, susceptibility to infections, and inflammatory responses.

Rational selection of 4,4',4″-(1,3,5-triazine-2,4,6-triyl) trianiline-based covalent organic framework as adsorbent for effective co-extraction of aflatoxins, zearalenone and its metabolites from food and biological samples.

Aflatoxins, zearalenone and its metabolites, as representative hazard mycotoxins cause adverse effects on food safety and human health. Developing a sensitive and reliable extraction and detection method is of great importance for monitoring their residue and exposure levels. In contrast to traditional trial-and-error selection steps, 4,4',4″-(1,3,5-triazine-2,4,6-triyl) trianiline covalent-bonding with 2,5-dihydroxyterephthalaldehyde, namely TAPT-OH-COF was screened as a potential adsorbent utilizing density functional theory calculations prior to the synthesis procedure. After experimental verification, magnetic TAPT-OH-COFs were prepared, characterized and applied for the extraction of aflatoxins, zearalenone and its metabolites from food and biological samples, coupled with high-performance liquid chromatography tandem mass spectrophy detection. Under the optimal conditions, the developed method exhibited low limits of quantification (0.05-0.50 µg/kg), satisfactory recoveries (75.8 %-110.9 %) and good precision with intraday and interday relative standard deviations (RSDs) not exceeding 12.2 %. This study may provide great potential for the selection of candidate adsorbents for multi-mycotoxins extraction from complex samples.

A novel micro-aqueous cold extraction of salmon head oil to reduce lipid oxidation and fishy odor: Comparison with common methods.

Traditional heat extraction (HE) has a low efficiency (75.2 wt%) and induces lipid oxidation of PUFAs. The novel micro-aqueous cold (<25 °C) extraction (MAE) was applied to extract salmon head oil. The recovery rate was 93.4 wt% at oil volume fraction Φ = 74 %. The extraction mechanism was agitation-induced droplet coalescence at an unstable and close-packing state (Φ = 74 %), increasing the portions of the large-sized droplets (>50 µm) from 2.8 vol% to 91.7 vol%. The MAE reduced the oil oxidation level and odor intensity compared to HE, although the lipid profile differed slightly. The HE head oil had more key fishy odor compounds, including hexanal (0.98 mg/kg), 3-methyl-butanal (0.25 mg/kg), 1-penten-3-ol (0.49 mg/kg), and 2-ethylfuran (0.19 mg/kg). The MAE oil had only 2-methyl-butanal (0.10 mg/kg) and 1-penten-3-ol (0.47 mg/kg). Overall, micro-aqueous extraction has great potential to replace industrial heat extraction with a better product quality.