Search

There is currently limited research on the structure-property relationship of reduction stimuli-responsive polymeric crosslinked micelles using mesoscopic simulations. Herein, dissipative particle dynamics (DPD) simulations were used to simulate the self-assembly process of the blank non-crosslinked micelle, the structure and doxorubicin (DOX) distribution of diselenide crosslinked micelle with different crosslinker contents (CCs) based on the nearest-neighbor bonding principle. The results revealed that the formation of a three-layer spherical micelle and the loaded DOX mainly distributed in the polycaprolactone (PCL) core and hydroxyethyl methacrylate (HEMA) mesosphere. The larger the dosage of DOX, the more DOX encapsulated, but the encapsulation of DOX in the hydrophobic domain would reach saturation when the dosage increased to 6.0 %. In micelles with lower CCs or crosslinking levels (CLs), DOX entered the middle layer and the inner core faster. Then, based on the nearest media-bead bond breaking principle and subsequently DPD simulation, the effects of different CCs on the micelle structure and DOX release properties were investigated. Low CC could cause fast drug release. With the increase of CCs, the micelle showed a slower DOX release trend. The multilayer crosslinked network system also affected the DOX release rate. Hence, this work can provide some mesoscale guidance for the structural design and structure-property relationship of stimuli-responsive reversible crosslinked micelles for drug delivery.

As a class of biocompatible and biodegradable naturally derived nanomaterials, cellulose nanocrystals (CNCs) with diverse surface functionalization have aroused considerable attention for a range of biomedical applications in drug or gene delivery, as a fluorescent nanoprobe, in cancer targeting, and in photothermal cancer therapy, among others. Herein, we construct the copolymer-functionalized CNCs as a pH- and near-infrared (NIR)-triggered drug carrier for simultaneous photothermal therapy and chemotherapy of cancer cells. Poly(ε-caprolactone)-ib/i-poly(2-(dimethylamino)ethyl methacrylate) (PCL-ib/i-PDMAEMA) was conjugated onto the surface of CNCs through ring-opening polymerization, followed by activators regenerated by electron transfer atom transfer radical polymerization (ARGET ATRP). The resultant CNC-based drug carrier can encapsulate doxorubicin (DOX) as a therapeutic agent and indocyanine green (ICG) as an NIR dye in the PCL core and the PDMAEMA shell, respectively, via hydrophobic and electrostatic interactions. In addition to the intrinsic pH response, the release profile of DOX can also be controlled by the duration of laser irradiation due to collapse of the crystal structure of the PCL domain with the increase of temperature induced by photothermal conversion. The drug carrier can exhibit enhanced cytotoxicity toward HepG2, human hepatocyte carcinoma, cells upon laser irradiation, which can be attributed to the synergistic effect arising from NIR-triggered burst release of DOX and photothermal heating. The rod-like morphology of the CNC-based drug carrier may help accelerate the endocytosis in cell membranes compared with its common spherical counterpart. Based on the abovementioned advantages, copolymer-functionalized CNCs can serve as a promising candidate for effective cancer treatment.

This study focuses on the transient liquid phase (TLP) bonding of DD5 single-crystal superalloy to CrCoNi-based medium-entropy alloy (MEA) using a BNi-2 filler alloy. The microstructure and mechanical properties of the TLP-bonded DD5/MEA joint were evaluated, and the microstructural evolution mechanism was investigated. The formation of the isothermal solidification zone (ISZ) depended on the diffusion of the melting-point depressants (Si and B elements) from the liquid filler into the DD5 and MEA substrates, as well as the dissolution of the substrates. Boron diffused along the γ channel of DD5 and reacted to form M5B3 boride, herein referred to as the diffusion-affected zone (DAZ I). Similarly, the Cr5B3 boride precipitated in the Ni-rich MEA matrix adjacent to the MEA substrate (i.e., DAZ II). Additionally, a coherent orientation of [0]BCT // [0 1 1]FCC and (0 0 2)BCT // (2 0 0)FCC was detected between M5B3 boride with a body-centered tetragonal (BCT) structure and the face-centered cubic (FCC) matrix. The performance of the joint was dominated by the properties of the bonding seam. As the bonding time increased from 20 to 80 min, the athermal solidification zone (including eutectic microstructure) was gradually replaced by the ISZ exhibiting excellent plastic deformation capability, and the shear strength of the joint was improved. The maximum shear strength (752 MPa) was achieved when the eutectic-free joint was bonded at 1050 °C for 80 min. The fracture morphology revealed a mixture mode, indicating the initiation of cracks in the DAZ II, mainly propagating in the ISZ, and passing through the DAZ I.

In this work, we predict two novel two-dimensional (2D) auxetic materials, BiSbX3 (X = S, Se) monolayers, through first-principles calculations. Attributed to their special braceletlike structure, the in-plane negative Poisson's ratio (NPR) of BiSbS3 and BiSbSe3 monolayers are as high as -0.25 and -0.26, respectively. The phonon dispersion calculations, ab initio molecular dynamics simulations, and elastic constants calculations demonstrate that these two monolayers possess excellent dynamic, thermal, and mechanical stabilities. The band gap values of BiSbS3 and BiSbSe3 calculated at the HSE level by considering the spin-orbit coupling (SOC) effect are 1.68 and 1.20 eV. The anisotropic carrier mobility and superior optical absorption indicate that they may shine in the next generation of electronic and optoelectronic devices. All of these discoveries not only enrich the types of auxetic materials but also provide a structural reference for designing new auxetic materials on the molecular level. Furthermore, they can provide theoretical guidance for future applications of BiSbX3 (X = S, Se) monolayers in various fields.

LiNi0.5Mn1.5O4 is a relatively promising high-voltage cathode material for lithium-ion batteries. In order to reduce the preparation cost and energy consumption of LiNi0.5Mn1.5O4, an innovative roasting process — non-constant temperature calcination — was proposed in this paper, and it is characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), laser particle size distribution test, cyclic voltammetry test, electrochemical impedance spectroscopy (EIS), first charge–discharge test, cyclic performance test, and comparative experiment. The research shows that this process avoids the high-temperature and constant-temperature stage, so as to effectively inhibit the growth and agglomeration of material particles, improve the electrochemical performance of the material, and reduce the production energy consumption and cost. It was found through experiments that the optimal heating rate is 2.0 °C/min. At this heating rate, the initial charge–discharge capacity reaches the maximum of 129.6 mAh/g, and the capacity decreases from 126 to 123.5 mAh/g (the capacity retention rate is 98%) after 100 cycles at 1 C.

Olivine-structured LiMnPO4 is one of the cathode materials with great application prospects for lithium-ion batteries in that it possesses the characteristics of abundant raw materials, low price, stable structure, high energy density, and good cycling stability. In this paper, the electronic structure of LiMn1-x-yFexNiyPO4 (x = 0, y = 0; x = 1/4, y = 1/4) system is calculated by using MS (Material Studio) software. The calculated results show that the band gap width of LiMn1/2Fe1/4Ni1/4PO4/C system is 0.105 eV, which has a great change compared with LiMnPO4. Thus, it is speculated that the Fe–Ni co-doped LiMnPO4 material has better electrochemical performance. The LiMn1-x-yFexNiyPO4 (x = 0, y = 0; x = 1/4, y = 1/4) composite materials were synthesized by co-precipitation method, and the optimum synthesis conditions also was explored. The electrochemical test indicates that the LiMn1/2Fe1/4Ni1/4PO4/C cathode material has excellent electrochemical properties, and its initial charge–discharge capacity is 143.8 mAh/g, which is significantly higher than that of LiMnPO4 material. The discharge capacity of this sample remains at about 152 mAh/g after 100 cycles at 0.05 C rate, showing good cyclic stability. The results of theoretical calculation and experimental test confirm each other, so as to prepare the LiMn1/2Fe1/4Ni1/4PO4/C materials with excellent electrochemical performance.

Aroused by plant photosynthesis, Z-scheme heterostructures have been considered as a potential photocatalyst for solar-driven water splitting to solve the current energy crisis. Hence, based on first-principles calculations, we predict that Sc2CF2/Janus MoSSe can be used as a Z-scheme heterostructure for efficient photocatalytic water splitting. The research shows that the traditional type-II to direct Z-scheme heterostructure conversion can be realized through different stacking methods of Sc2CF2 and Janus MoSSe. Through the built-in electric field and band bending theory, the transition path of photogenerated carriers is analyzed, which reveals the completely different photocatalytic mechanism of type-II and direct Z-scheme heterostructure. Surprisingly, the direct Z-scheme heterostructure displays a high overpotential of the hydrogen evolution reaction ( χ H 2 =1.01 eV) and the oxygen evolution reaction ( χ O 2 =1.46 eV) compared with the type II heterostructure. More importantly, the direct Z-scheme heterostructure has an ultra-high solar-to-hydrogen (STH) efficiency (36.1%), which breaks through the limitation of traditional theoretical efficiency and reveals a tremendous prospect of commercial application. Furthermore, the calculation of free energy confirms that the water splitting reaction on the direct Z-scheme heterostructure occur spontaneously under the external potential, but not for type-II heterostructure. Finally, introducing the additional electronic conductor (N-doped graphene) can accelerate the electron (hole) transfer and interlayer carrier recombination, which will further improve the photocatalytic performance of Z-scheme heterostructure. These distinctive features make Sc2CF2/Janus MoSSe heterostructure as promising Z-scheme photocatalyst for water splitting.

The gas-sensing performance of PbSnS2 monolayer to sulfur hexafluoride (SF6) decompositions (SO2, H2S, HF, SOF2, and SO2F2) has been systematically studied by density functional theory and nonequilibrium Green’s function calculations. The most stable adsorption configurations, adsorption energies, charge transfer, electron localization function (ELF), density of states (DOS), and ${I}$ – ${V}$ curves of gas molecules on PbSnS2 are calculated and discussed. SO2 exhibits the largest adsorption energy of −0.74 eV with the charge transfer of −0.39 e and HF possesses the biggest charge transfer of −0.66 e with the adsorption energy of −0.46 eV. The results of ELF and DOS show that the interaction between SO2 and PbSnS2 may be stronger than those of other gases. Moreover, ${I}$ – ${V}$ curves show that the responses of PbSnS2 to SO2 is up to 65.5% at the bias of 2.2 V. Therefore, PbSnS2 monolayer may be a qualified material for detecting SF6 decompositions.

In this work, we explore the application potential of AsP/M2CO2 (M = Sc, Zr) van der Waals heterostructures in photocatalytic water splitting through the first-principles calculations. The calculated results show that AsP/Zr2CO2 heterostructure possesses an unfavorable type-Ⅰ band alignment, whereas AsP/Sc2CO2 exhibits a desirable type-Ⅱ band alignment, which is beneficial for separating the photogenerated electron-hole pairs. Also, the band edge positions of AsP/Sc2CO2 heterostructure stride the redox potential of water, ensuring favorable reaction kinetics. Besides, the strong optical absorption of AsP/Sc2CO2 heterostructure in both visible and ultraviolet regions (especially up to 10−6 cm−1 at about 250 nm) makes it possible to utilize solar energy effectively. Meanwhile, AsP/Sc2CO2 heterostructure has an exciton binding energy as low as 0.09 eV, which quantitatively illustrates the high separation efficiency of photogenerated charge carrier. Thus, the type-Ⅱ band alignment, suitable band edge position, strong light absorption, and low exciton binding energy together indicate that AsP/Sc2CO2 heterostructure is a potential photocatalytic material. In addition, the obvious redshift phenomenon in the optical spectrum of AsP/Sc2CO2 heterostructure shows that biaxial strain can improve its light capture capability. Also, the interconversion between type-Ⅱ and type-Ⅰ can be achieved by applying different strains. All these findings suggest that the novel AsP/Sc2CO2 heterostructure has significant application prospects in next-generation photovoltaic and photocatalytic devices.

This paper deals with the free and forced, linear and nonlinear vibration of functionally graded (along with thickness) nanotube, considering the non-uniform cross-section that made a two-dimension...

Waist-to-height ratio (WHtR) is a controversial evaluation index of cardiovascular risk factors (CVRFs) in children and adolescents. To assess the accuracy of WHtR as a measure to screen for clusters of at least one CVRF (CVRF1), two CVRFs (CVRF2), and three CVRFs (CVRF3) in different ages, sexes, regions and cut-offs. The PubMed, Web of Science, EBSCOhost, Springer, Taylor & Francis Online, Wiley Online Library, Wanfang, and CNKI databases were searched for eligible publications up to June 2021. The QUADAS-2 checklist was used to assess the methodology of the included studies. Twenty-two studies that evaluated 85281 children and adolescents aged 5–19 years were included in the meta-analysis. The AUSROC values were 0.56 (95% CI: 0.54–0.57), 0.82 (95% CI: 0.81–0.83), and 0.89 (95% CI: 0.89–0.90) for CVRF1, CVRF2, and CVRF3, respectively. Higher AUSROC values were found for adolescents (12–19 years), that is, 0.91 (95% CI: 0.88–0.93), 0.90 (95% CI: 0.87–0.92) for males, and 0.91 (95% CI: 0.90–0.91) for a cut-off of ≥ 0.51 in the identification of CVRF3. WHtR can be used as an accurate screening tool for CVRF3 and CVRF2 in children and adolescents, and it is recommended to select different cut-offs according to different ages, sexes, and regions.

Background At present, Astragalus mongholicus products on the market represent two growth patterns: imitative wild A. mongholicus (WAM) and cultivated A. mongholicus (CAM). The 6-year-old WAM (A6) and 2-year-old CAM (B2) products are often sold as commodities. This study aimed to explore the effects of the abovementioned growth patterns on the biosynthetic mechanisms of isoflavone accumulation in A. mongholicus products. Results In this paper, the content of calycosin-7-O-β-D-glucoside in 6-year-old WAM (A6) was significantly higher than that in 2-year-old CAM (B2) based on high-performance liquid chromatography. Tissue anatomy indicated that A6 has developed phloem fibers, thickened secondary walls, and a more well-developed vascular system than B2. Thirteen differentially accumulated metabolites were found in A6 and B2 by UHPLC-ESI-Q-TOF-MS/MS, of which isoflavones were highly and significantly enriched in A6. By combining transcriptomics and metabolomics analysis, we found that the metabolomics profile was the same as the transcriptomics profile in both A6 and B2. In total, 11 novel isoflavone-related genes were isolated using BLAST and functional annotation through RNA-Seq and Iso-Seq. The results of integrated analysis, Short Time-series Expression Miner analysis, and Pearson correlation analysis showed that the regulation of four key enzymes, cinnamate 4-hydroxylase, 6-deoxychalcone synthase, chalcone reductase, and chalcone isomerase, led to the high accumulation of isoflavones in A6. In addition, AmUFGT (c778119) and AmUCGT (c303354) were predicted to be 7-O-glycosyltransferases by phylogenetic analysis; these genes catalyze formononetin and calycosin, respectively. Conclusions The findings of this work will clarify the differences in the biosynthetic mechanism of isoflavone accumulation between A6 and B2, which will guide the cultivation of A. mongholicus.

Mandarin fish (Siniperca chuatsi) during fermentation presents a unique elastic texture. In this investigation, the physicochemical and gel-forming properties of fish proteins were evaluated to explain the formation of elastic characteristics. During fermentation, the combined effects of acidification by Lactobacillus sake SMF-L5, increased sodium chloride, and decreased moisture content in the fish protein generated a suitable microenvironment for gelation. The mass transfer of sodium chloride was accompanied by NMR relaxation of the immobilized water. The ripening fermented fish had a functionally available MHC, a higher fractal dimension, and a stable α-helical structure. Also, it exhibited excellent gel-forming performances, mainly including garlic-cloves shaped protein gel, stronger springiness, and enhanced L* and whiteness. Correlation analysis showed that the gel's physical properties were differently related to the protein's physicochemical characteristics except for total free amino acids. These results could lay a theoretical foundation for the gel formation mechanism of fermented mandarin fish.

The tumor microenvironment (TME), which is regulated by intrinsic oncogenic mechanisms and epigenetic modifications, has become a research hotspot in recent years. Characteristic features of TME include hypoxia, metabolic dysregulation, and immunosuppression. One of the most common RNA modifications, N6-methyladenosine (m6A) methylation, is widely involved in the regulation of physiological and pathological processes, including tumor development. Compelling evidence indicates that m6A methylation regulates transcription and protein expression through shearing, export, translation, and processing, thereby participating in the dynamic evolution of TME. Specifically, m6A methylation-mediated adaptation to hypoxia, metabolic dysregulation, and phenotypic shift of immune cells synergistically promote the formation of an immunosuppressive TME that supports tumor proliferation and metastasis. In this review, we have focused on the involvement of m6A methylation in the dynamic evolution of tumor-adaptive TME and described the detailed mechanisms linking m6A methylation to change in tumor cell biological functions. In view of the collective data, we advocate treating TME as a complete ecosystem in which components crosstalk with each other to synergistically achieve tumor adaptive changes. Finally, we describe the potential utility of m6A methylation-targeted therapies and tumor immunotherapy in clinical applications and the challenges faced, with the aim of advancing m6A methylation research.

Astragaloside IV (AS-IV) is a representative component of astragaloside saponins in dried roots of Astragali Radix. Astragaloside possesses a broad spectrum of pharmacological activities, including antibacterial, anti-fibrosis, antioxidant, anti-inflammatory, and neuroprotective effects. However, the role of AS-IV in antiaging remains unclear. In this article, we studied the function of AS-IV in antiaging by using the Caenorhabditis elegans (C. elegans) model. We showed that AS-IV can prolong the lifespan of C. elegans in a natural aging model, a paraquat injury model, and a heat stress model and improve the movement capacity of nematodes. 1H-NMR data indicate an improvement of glutamate content and a decrease in glucose in the AS-IV treatment group compared with the control. Further investigation revealed that AS-IV can induce the mRNA expression of superoxide dismutase (SOD) and catalase (CAT) genes and increase the activities of SOD and CAT in the nematode. Interestingly, AS-IV could not extend the lifespan of sod-1, sod-2, sod-3, sod-4, sod-5, ctl-1, ctl-2, ctl-3, and daf-16 mutants. These data indicate that AS-IV prevents aging via mainly improving age-related functional declines, the antioxidant capacity of nematodes and partially modulating the insulin/insulin growth factor 1 signaling pathway activity. Our results provide new insights into how AS-IV prevents and treats aging.

It is found that many two-dimensional materials are easy to obtain out-of-plane piezoelectric properties because of their Janus structure. Here, based on the monolayer GeSe and SnSe, we study the electronic structure and piezoelectricity of the Janus M2SeX (M=Ge, Sn; X=S, Te) monolayers. Due to the lack of inversion symmetry and mirror symmetry, as well as flexible mechanical properties, the 2D Janus M2SeX monolayers have large in-plane piezoelectric coefficients d11 (up to 345.08pm/V) and out-of-plane piezoelectric coefficients d31 (up to 3.83pm/V). All energy band structures of two-dimensional (2D) Janus M2SeX monolayers show indirect bandgap and Zeeman-type spin splitting after considering spin orbit coupling (SOC). The lack of mirror symmetry leads to out-of-plane spin polarization. In addition, the calculation based on the deformation potential theory shows that the 2D Janus M2SeX monolayers have high carrier mobility. The large piezoelectric properties and high carrier mobility show the application potential of 2D Janus M2SeX monolayers in flexible electronic devices and piezoelectric devices.

A chiral nematic mesoporous molybdenum carbide film (CN-Mo2C) was fabricated through the self-assembly of cellulose nanocrystal with peroxomolybdate. CN-Mo2C exhibits a tunable chiral nematic structure by varying the ratio of constituents, enabling a surface area of 210 m2 g−1. Importantly, it shows a typical chiroptical feature through polarized optical microscopy and circular dichroism spectral analysis. As it has an excellent conductivity of 2.4 × 10−2 S cm−1, we try to use CN-Mo2C in the electrocatalytic HER production, presenting an efficient H2 production capacity. It is a versatile synthetic strategy that can conveniently enable other large-area macroscopic chiral metal-based materials.

In this study, the adsorption of gas molecules, such as O2, NH3, CO, CO2, H2O, NOx (x = 1, 2) and SO2, on Janus Te2Se monolayer has been investigated by means of density functional theory (DFT) calculations. We show that Janus Te2Se monolayer is preferable for SO2 and NOx molecules with suitable adsorption strength and apparent charge transfers. We further calculated the current-voltage (I-V) curves using the nonequilibrium Green's function (NEGF) method. The transport feature exhibits distinct responses with a dramatic change of I-V curves before and after NOx (SO2) adsorption on Janus Te2Se. Thus, we predict that Janus Te2Se could be a promising candidate for SO2 and NOx sensors with high selectivity and sensitivity. Moreover, the effect of strain on the gas/substrate adsorption systems was also studied, implying that the strained Janus Te2Se monolayer could enhance the sensitivity and selectivity to SO2 and NO2. The adsorbed SO2 and NO2 on Janus Te2Se could escape by releasing the applied strain, which indicates that the capture process is reversible. Our study widens the application of Janus Te2Se not only as piezoelectric materials, but also as a potential gas sensor or capturer of SO2 and NOx with high sensitivity and selectivity.

A phosphopeptide-modified nanochannel was prepared based on a conical polymeric nanopore. It shows a reversible Ca2+-induced inactivation effect toward the ion flow and molecular transport, resulting from Ca2+ binding-caused surface charge neutralization and hydrophilicity reduction, and Ca2+ removal by the competitive binding.

Two-dimensional Janus nanomaterials, due to their unique electronic, optical, and piezoelectric characteristics resulting from the antisymmetric structures, exhibit great prospects in multifunctional energy application to alleviate the energy crisis. Monolayer Janus Pb2SSe, with a black phosphorus-like structure and an indirect band gap of 1.59 eV as well as high carrier mobility (526-2105 cm2 V-1 s-1), displays outstanding potentials in the energy conversion between nanomechanical energy, solar energy, waste heat, and electricity, which has been comprehensively studied utilizing DFT-based simulations. The research results reveal that monolayer Pb2SSe not only possesses giant in-plane piezoelectricity of d11 = 75.1 pm V-1 but also superhigh out-of-plane piezoelectric coefficients (d31 = 0.5 pm V-1 and d33 = 15.7 pm V-1). Meanwhile, by constructing Pb2SSe bilayers, the out-of-plane piezoelectric coefficients can be significantly enhanced (d31 = 19.2 pm V-1 and d33 = 194.7 pm V-1). In addition, owing to the small conduction band offset, suitable donor band gap and excellent light absorption capability in the Pb2SSe/SnSe (Pb2SSe/GeSe) heterostructure, the power conversion efficiencies were calculated to be up to 20.02% (Pb2SSe/SnSe) and 19.28% (Pb2SSe/GeSe), making it a promising candidate for solar energy collection. Furthermore, from the thermoelectric electron and phonon transport calculations, it can be found that the Pb2SSe monolayer is an n-type thermoelectric material with ultrahigh ZT = 2.19 (1.52) at room temperature, which can be traced back to its ultralow κL = 0.78 (0.99) W m-1 K-1, and superhigh PF = 10.18 (8.25) mW m-1 K-2 along the x(y) direction at the optimal doping concentration at 300 K. The abovementioned versatile characteristics in the Janus Pb2SSe monolayer, along with its comprehensive stabilities (energy, dynamic, thermal, and mechanical stabilities), highlight its potential in clean energy harvesting.

Astragali Radix is the dry root of the leguminous plants

Klebsiella pneumoniae is a leading cause of severe infections in humans and animals, and the emergence of multidrug-resistant strains highlights the need to develop effective vaccines for preventing such infections. Live attenuated vaccines are attractive vaccine candidates available in the veterinary field. We recently characterized that the K. pneumoniae kbvR (Klebsiella biofilm and virulence regulator) mutant was a highly attenuated strain in the mice model. In the present study, the characterization, safety, and protective efficacy of ΔkbvR strain as a live attenuated vaccine were evaluated. The synthesis and activity of type 1 fimbriae were increased in the ΔkbvR strain. All mice inoculated by the subcutaneous route with 105, 106, and 107 colony-forming units (CFU) doses of the ΔkbvR strain survived. Subcutaneous immunization with two doses of 105 or 107 CFU ΔkbvR elicited a robust humoral immune response, and provided protection against the following K. pneumoniae intraperitoneal infection. The antisera of mice immunized with 105 CFU dose improved the opsonophagocytic ability and complement-mediated lysis not only to the same serotype strain but also to the different serotype strain. The passive transfer of antisera from 105 CFU dose-immunized mice provided protection against K. pneumoniae infection. Overall, our results suggest the great potential of the ΔkbvR strain as a novel vaccine candidate against K. pneumoniae infections in herds or humans.

Klebsiella pneumoniae is considered a global threat because of the rising prevalence of multidrug-resistant strains and their optimal adaptation to clinical environments and the human host. The sensing and adaption abilities of bacteria to the environmental osmotic stress can change the expression of their outer membrane porins, membrane permeability, and resistance to antibiotics.

The tumor microenvironment (TME), which is regulated by intrinsic oncogenic mechanisms and epigenetic modifications, has become a research hotspot in recent years. Characteristic features of TME include hypoxia, metabolic dysregulation, and immunosuppression. One of the most common RNA modifications, N6-methyladenosine (m

As an important component of the immunosuppressive tumor microenvironment (TME), it has been established that mesenchymal stem cells (MSCs) promote the progression of tumor cells. MSCs can directly promote the proliferation, migration, and invasion of tumor cells via cytokines and chemokines, as well as promote tumor progression by regulating the functions of anti-tumor immune and immunosuppressive cells. MSCs-derived extracellular vesicles (MSCs-EVs) contain part of the plasma membrane and signaling factors from MSCs; therefore, they display similar effects on tumors in the immunosuppressive TME. The tumor-promoting role of macrophage migration inhibitory factor (MIF) in the immunosuppressive TME has also been revealed. Interestingly, MIF exerts similar effects to those of MSCs in the immunosuppressive TME. In this review, we summarized the main effects and related mechanisms of tumor-associated MSCs (TA-MSCs), TA-MSCs-EVs, and MIF on tumors, and described their relationships. On this basis, we hypothesized that TA-MSCs-EVs, the MIF axis, and TA-MSCs form a positive feedback loop with tumor cells, influencing the occurrence and development of tumors. The functions of these three factors in the TME may undergo dynamic changes with tumor growth and continuously affect tumor development. This provides a new idea for the targeted treatment of tumors with EVs carrying MIF inhibitors.

Red pitaya peel (RPP) is a good source of polysaccharides, which can be used in the production of biodegradable material. Betacyanins in it possess antioxidant and pH-sensitive properties. However, RPP is commonly discarded during fruit processing. This study aimed to develop real-time intelligent film using RPP to evaluate pork freshness.Real-time intelligent films were developed with film-forming substrates (FFS) composed of 60-100% (w/w) RPP and 0-4% (v/w) glycerol in pH 4.3 ~ 8.0. Rheology tests revealed that the FFS exhibited shear-thinning behavior. Fourier-transform infrared (FTIR) analysis showed that molecules in the RPP interacted with glycerol and formed hydrogen bonds. It showed that the film developed with FFS of 80% RPP and 2% (v/w) glycerol had strong molecular interaction, dense structure, and optimal tensile strength and elongation at break. Film with pH adjusted to 7.0 had greater sensitivity to ammonia than film that was prepared at an original pH of 4.3, so this film was used to monitor freshness of pork. A visible change in the color of the film was observed during the spoiling process of pork, which correlated with the accumulated total volatile base nitrogen.Based on its sensitivity to ammonia, the film made of 80% (w/w) RPP and 2% (v/w) glycerol at pH 7.0 was recommended for use in monitoring the freshness of protein-rich food. Our findings are of great significance for ensuring meat quality and safety and for reducing food waste. © 2022 Society of Chemical Industry.

All cells, including prokaryotes and eukaryotes, could release extracellular vesicles (EVs). EVs contain many cellular components, including RNA, and surface proteins, and are essential for maintaining normal intercellular communication and homeostasis of the internal environment. EVs released from different tissues and cells exhibit excellent properties and functions (e.g., targeting specificity, regulatory ability, physical durability, and immunogenicity), rendering them a potential new option for drug delivery and precision therapy. EVs have been demonstrated to transport antitumor drugs for tumor therapy; additionally, EVs' contents and surface substance can be altered to improve their therapeutic efficacy in the clinic by boosting targeting potential and drug delivery effectiveness. EVs can regulate immune system function by affecting the tumor microenvironment, thereby inhibiting tumor progression. Co-delivery systems for EVs can be utilized to further improve the drug delivery efficiency of EVs, including hydrogels and liposomes. In this review, we discuss the isolation technologies of EVs, as well as engineering approaches to their modification. Moreover, we evaluate the therapeutic potential of EVs in tumors, including engineered extracellular vesicles and EVs' co-delivery systems.

Based on the tumor microenvironment with weak acidic characteristics, a nano-drug delivery system that achieves controlled release of drugs through the pH response has been a popular strategy to improve the effectiveness of tumor therapy and reduce toxic side effects, and combining photothermal therapy (PTT) on this basis can help improve the antitumor effect. In this study, mesoporous silica nanoparticles (MSNs) were surface-modified with polymer poly(PEGMA