Baggerslaughter4026
Polysaccharide/MOF composite membranes have captured the interests of many researchers during decontamination of polluted environments. Their popularity can be attributed to the relatively high chemical and thermal stabilities of these composite membranes. Chitosan is among the polysaccharides extensively used during the synthesis of hybrid membranes with MOFs. The applications of chitosan/MOF composite membranes in separation science are explored in detail in this paper. Researchers have also synthesised mixed matrix membranes of MOFs with cellulose and cyclodextrin that have proved to be effective during separation of a variety of materials. The uses of cellulose/MOF and cyclodextrin/MOF membranes for the removal of environmental pollutants are discussed in this review. In addition, the challenges associated with the use of these mixed matrix membranes are explored in this current paper.In recent years, smart-responsive nanocellulose composite hydrogels have attracted extensive attention due to their unique porous substrate, hydrophilic properties, biocompatibility and stimulus responsiveness. At present, the research on smart response nanocellulose composite hydrogel mainly focuses on the selection of composite materials and the construction of internal chemical bonds. The common composite materials and connection methods used for preparation of smart response nanocellulose composite hydrogels are compared according to the different types of response sources such as temperature, pH and so on. The response mechanisms and the application prospects of different response types of nanocellulose composite hydrogels are summarized, and the transformation of internal ions, functional groups and chemical bonds, as well as the changes in mechanical properties such as modulus and strength are discussed. Finally, the shortcomings and application prospects of nanocellulose smart response composite hydrogels are summarized and prospected.Cellulose has attracted an increasing attention for piezoelectric energy harvesting. However, the limited piezoelectricity of natural cellulose constraints the applications. Therefore, we demonstrate the development of piezoelectric nanogenerators based on robust, durable layered membranes composed of cotton cellulose interfaced maleic-anhydride-grafted polyvinylidene fluoride (PVDF-g-MA) nanofibers. Exploiting polydopamine@BaTiO3 (pBT) nanoparticles as interlayer bridges, interlocked layer-layer interfaces that covalently bind component layers are constructed by a facile and scalable approach. As-obtained membranes exhibit significantly improved piezoelectricity with a maximum piezoelectric coefficient of 27.2 pC/N, power density of 1.72 μW/cm2, and stability over 8000 cycles. Substantial enhancement in piezoelectricity over pristine cellulose is ascribed to the synergy of components and the localized stress concentration induced by pBT nanoparticles. The self-powered device could also be used to detect human physiological motions in different forms. Such cellulose-based membranes can be up-scaled to fabricate ecofriendly, flexible and durable energy harvesters and self-powered wearable sensors.Trichinellosis caused by Trichinella spiralis is a serious zoonosis with a worldwide. ASN007 β-Glucans (BG) are readily used across the world with noted health benefits, yet the effect and mechanism of BG on host defense against helminth infection remain poorly understood. We observed that BG could trigger worm expulsion via mucus layer independently of type 2 immunity, but was dependent on the gut microbiota in mice. BG restored the abundance of Bacteroidetes and Proteobacteria changed by T. spiralis infection to the control group level and markedly increased the relative abundance of Verrucomicrobia. Akkermansia (belonging to Verrucomicrobia) were significantly expanded in the BG + T. spiralis group. Notably, daily oral supplementation of pasteurized A. muciniphila has a stronger deworming effect than live bacteria and interacted with TLR2. These findings of this study is an easily implementable strategy to facilitate expulsion of gastrointestinal helminth.In this paper, a reinforced Biomass Gel Artificial Muscle (BGAM) was fabricated by natural polysaccharide of Sodium Alginate (SA) doped with an Ionic Liquid (IL) of 1-ethyl-3-methylimidazolium tetrafluoroborate ([EMIm][BF4]). Micro-nano regulation effect and reinforcement mechanism of IL doping content on electromechanical response performance of BGAM were researched during a single cycle and repeated cycles. Then, a green fabrication process and a set of valid test methods for BGAM were proposed in detail. The experimental results showed that when IL doping content was 4 mL, the BGAM achieved optimal modification, with a porosity of 70.47%, where it internally adopted the porous polymer structure of ion channels. Additionally, specific capacitance of BGAM attained a maximum value of 126.98 mF/g, and the inner resistance and elastic modulus reached minimum values of 2.018 Ω and 1.871 MPa, separately. Thus, the optimal working life and output-force density values, namely, 1720 s and 13.072 mN/g, respectively, were also determined for the BGAM.Consumption of chitooligosaccharides (COS) prevents intestinal microecological disorder. The mechanisms for the effects of different COS on the gut microbiota are currently unclear. This study examined the impact of COS with different degrees of polymerization (DPs) on the gut microbial community and metabolic profile. COS significantly promoted the growth of Bacteroidetes, and inhibited that of Proteobacteria, which were significantly correlated with DPs. COS3 and COS2 enriched the butyrate production in microbial communities composed of Clostridium and Parabacteroides. Microbial communities enriched by DPs 4-6 COS displayed increased diversity in differential metabolite function. Several biomarkers were distinguished significantly, including unsaturated fatty acids, bile acids, indoles and amines, which are mainly related to processes such as fatty acid synthesis and decomposition, bile acid modification, and tryptophan metabolism. The results display the relationship among COS structure-gut microbes-metabolomics, providing a new perspective for COS as a functional food to improve intestinal health.Chemo-photothermal combination therapy has great promise for enhanced tumor treatment. Hereby, we developed a complex nanoparticle using electrostatic absorption method, in which the inner chitosan (CS) NPs loaded polypyrrole (PPy) nanoparticles and 5-fluorouracil (5Fu), the outer shell was carboxymethyl cellulose (CMC) crosslinked with disulfide. The drug loaded polysaccharide complex nanoparticles displayed good photothermal effects, and the drug release would be triggered by multi-model response of NIR irradiation, high glutathione (GSH) and weak acidity in tumor environment. In vitro biological studies indicated the nanopartiles could be effectively internalized by HepG2 cancer cells. Moreover, the remarkable inhibition of the CMC complex PPy and 5Fu loaded CS nanoparticles (CMC/CS@PPy + 5Fu NPs) against tumor growth was achieved in HepG2-bearing mice model, suggesting its great potential for synergetic chemo-photothermal therapy.Chitin, an abundant, biodegradable, and biocompatible polysaccharide, is one of the most ideal eco-friendly alternatives to petroleum-based plastics. However, the applications of chitin-based materials are hindered by their low processability and brittleness induced by strong hydrogen bonds. Herein, a tensile-induced orientation and hydrogen bond reconstruction strategy was developed to fabricate a chitin nanowhiskers/poly(vinyl alcohol) composite film with high strength and toughness. After stretching and hydrogen bond reconstruction, the tensile strength and elongation at break of the composite film increased from 38.6 to 115.2 MPa and 9.37% to 40.7%, respectively. Furthermore, strengthening and toughening mechanisms were also studied, which were attributed to the effects of the intra-layer orientation and interlayer sliding, respectively.Ternary cyclodextrin (CD) complexes (drug/CD/polymer) can effectively improve the solubility of water-insoluble drugs with large size than binary CD formulations. However, ternary formulations are screened by a trial-and-error approach, which is laborious and material-wasting. Current research aims to develop a prediction model for ternary CD formulations by combined machine learning and molecular modeling. 596 ternary formulations data were collected to build a prediction model by machine learning. The random forest model achieved good performance with R2 = 0.887 in ST prediction and R2 = 0.815 in ST/SB prediction. Two ternary formulations (Hydrocortisone/β-CD/HPMC and dovitinib/γ-CD/CMC) were used to validate the prediction model. Molecular modeling results showed that HPMC not only warped around hydrocortisone but also prevented CD molecules from self-aggregation to increase solubility. In conclusion, a prediction model for the ternary CD formulations was successfully developed, which will significantly accelerate the formulation screening process to benefit the formulation development of water-insoluble drugs.High amylose starch nanoparticles (HS-SNPs) were rapidly synthesised by high-speed circumferential force of homogenisation (3000 and 15,000 rpm) during nanoprecipitation. Morphology and dynamic light scattering analyses showed that HS-SNPs fabricated by stronger circumferential shearing were excellent stabilisers in smaller sizes (20-50 nm). Their aggregates were liable to separate in the aqueous phase with the nano effect under either homogenisation over 6 min or ultrasonication in 2 min. SNP-based nanoemulsion ( less then 200 nm) of high-water fraction was achieved, though the high hydrophilicity of the SNPs were identified by the contact angle. For homogenisation (with 100-2000 nm emulsion size), only time prolongation led to a better dispersion of SNP aggregates. Ultrasonication with periodic cavitation could disintegrate SNP aggregates into micro-aggregates for a stable emulsion system in a short period. In contrast, long-term ultrasound caused simultaneous re-agglomeration and solubilisation of the SNPs, leading to weakened interface barriers and decreased storage stability.We prepared super-hydrophobic nanocellulose films using a non-toxic octadecylamine/polydopamine system. Octadecylamine, a low surface energy material, was used to provide hydrophobic alkyl long chains. Polydopamine was produced by dopamine under alkaline conditions, creating an adhesive substance, which reinforced the hydrophobic long chains and increased the surface roughness of nanocellulose. The effects of reagent concentration, reaction temperature, and reaction time on hydrophobicity were then investigated. The results showed that with a 11 mass ratio of nanocellulose to octadecylamine, and reacting at 60 °C for 4 h, the contact angle of the obtained composite membrane reached 168.2°. Scanning electron microscope images revealed that the modified nanocellulose had a smaller particle size and more uniform distribution, which effectively improved the hydrophobicity of the nanocellulose. Thus, the green preparation of superhydrophobic films with high-temperature resistance and wear resistance was realized, which contributed to the high-value utilization of nanocellulose.