Timmschroeder7564

Mushroom d-glucans are recognized as dietary fibers and as biologically active natural polysaccharides, with the advantages of being quite inexpensive for production, tolerable, and having a range of possible structures and physicochemical properties. The prebiotic potential of mushroom d-glucans has been explored in recent years, but the relationship between their various structural features and activity is poorly understood. This review focuses on comprehensively evaluating the prebiotic potential of mushroom d-glucans in face of their structural variations. Overall, mushroom d-glucans provide a unique set of different structures and physicochemical properties with prebiotic potential, where linkage type and solubility degree seem to be associated with prebiotic activity outcomes. The understanding of the effects of distinct structures and physicochemical properties in mushroom d-glucans on the gut microbiota contributes to the design and selection of new prebiotics in a more predictable way.Successful treatment of skin infections requires eradication of biofilms found in up to 90 % of all chronic wounds, causing delayed healing and increased morbidity. We hypothesized that chitosan hydrogel boosts the activity of liposomally-associated membrane active antimicrobials (MAA) and could potentially improve bacterial and biofilm eradication. Therefore, liposomes (∼300 nm) bearing chlorhexidine (CHX; ∼50 μg/mg lipid) as a model MAA were incorporated into chitosan hydrogel. The novel CHX-liposomes-in-hydrogel formulation was optimized for skin therapy. It significantly inhibited the production of nitric oxide (NO) in lipopolysaccharide (LPS)-induced macrophage and almost completely reduced biofilm formation. Moreover, it reduced Staphylococcus aureus and Pseudomonas aeruginosa adherent bacterial cells in biofilm by 64.2-98.1 %. Chitosan hydrogel boosted the anti-inflammatory and antimicrobial properties of CHX.A direct production route of cellulose nanofibers (TOCN-D) from raw wood particles of paulownia using simultaneous bleaching and TEMPO oxidation process was specifically investigated and introduced. For comparison, we prepared cellulose nanofibers (TOCN-C) through a common route of TEMPO oxidation of cellulose fibers, and cellulose nanofibers with disk grinding (GCNF). FE-SEM analysis showed that the average diameter of TOCN-D (5 ± 3 nm) was similar to that of TOCN-C (6 ± 3 nm). XRD results confirmed that the crystal properties of TOCN-D and that of TOCN-C were almost the same. TOCN-D and TOCN-C showed similar chemical, thermal and optical properties in FTIR, TGA and transparency tests, respectively. The nanopaper made from TOCN-D showed high Young's modulus (13.8 GPa) and tensile strength (233 MPa), which were similar to those of TOCN-C nanopaper. Owing the aforementioned similarities, it is concluded that the TOCN-D produced through direct route is a technically, environmental-friendly and economically valuable product.Antibacterial property for scaffolds is an urgent problem to prevent infections in bone repair. Ag nanoparticles possess excellent bactericidal activities, whereas their agglomeration restricts the full play of antibacterial property in scaffold. Herein, a mace-like nanosystem was constructed to improve their dispersion by in-situ growth of Ag nanoparticles on cellulose nanocrystal (CNC), which was labeled CNC@Ag nanosystem. Subsequently, the CNC@Ag nanosystem was introduced into poly-L-lactide (PLLA) scaffolds. Results demonstrated that the nanosystem uniformly dispersed in scaffold. The antibacterial tests demonstrated that the scaffolds possessed robust antibacterial activities against E. coli, with bacterial inhibition rate over 95%. Moreover, ion release behavior corroborated the scaffolds continuously released Ag+ for more than 28 days, which benefited from the immobilization effect of CNC on Ag. Encouragingly, the mechanical properties of the scaffolds were remarkably higher than that of PLLA/CNC scaffolds, owing to the mace-like CNC@Ag nanosystem improved the load transfer efficiency in the scaffold.Inspired by muscle architectures, double network hydrogels with hierarchically aligned structures were fabricated, where cross-linked cellulose nanofiber (CNF)/chitosan hydrogel threads obtained by interfacial polyelectrolyte complexation spinning were collected in alignment as the first network, while isotropic poly(acrylamide-co-acrylic acid) (PAM-AA) served as the second network. After further cross-linking using Fe3+, the hydrogel showed an outstanding mechanical performance, owing to effective energy dissipation of the oriented asymmetric double networks. The average strength and elongation-at-break of PAM-AA/CNF/Fe3+ hydrogel were 11 MPa and 480 % respectively, which the strength was comparative to that of biological tissues. The aligned CNFs in the hydrogels provided probable ion transport channels, contributing to the high ionic conductivity, which was up to 0.022 S/cm when the content of LiCl was 1.5 %. Together with superior biocompatibility, the well-ordered hydrogel showed a promising potential in biological applications, such as artificial soft tissue materials and muscle-like sensors for human motion monitoring.The contribution of ATR-FTIR spectroscopy to study cell wall polysaccharides (CWPs) was carefully investigated. The region 1800-800 cm-1 was exploited using principal component analysis and hierarchical clustering on a large range of different powders of CWPs based on their precise chemical characterization. Relevant wavenumbers were highlighted for each CWP 1035 cm-1 was attributed to xylose-containing hemicelluloses, 1065 and 807 cm-1 to mannose-containing hemicelluloses, 988 cm-1 to cellulose, 1740 and 1600 cm-1 to homogalacturonans according to the degree of methylation. CQ211 mouse Some band positions were affected by macromolecular arrangements (especially hemicellulose-cellulose interactions). However, as arabinan and galactan did not reveal distinctive absorption bands, ATR-FTIR spectroscopy did not allow the discrimination of cell walls differing by the abundance of these polysaccharides, e.g., those extracted from apple and beet. Therefore, the application of ATR-FTIR could remain sometimes limited due to the complexity of overlapping spectra bands and vibrational coupling from the large diversity of CWP chemical bonds.