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This study provided a useful approach for future development of novel heparin-derivative medications.Herein, we report on a transparent, water-stable, high oxygen barrier packaging film made from a combination of cellulose nanofiber (CNF) and a fluoropolymer (FP) coating. Nanofibrillation of the hardwood kraft pulp was carried out using succinic anhydride pretreatment and aqueous counter collision (ACC) technique to obtain ultrafine (5-7 nm) succinylated cellulose nanofibers (SCNF), which was readily fabricated into a thin coating (on PET film) as well as a self-standing film. Introducing the FP topcoat on SCNF enabled a synergistic enhancement of both oxygen barrier performance and stability against water-swelling.Biobased tractable films consisting of blends of chitosan (CS) with polymer bearing carbazole derivatives as pendant groups and fluorene-thiophene as donor-acceptor units (referred to as DA) were prepared, and their optical, morphological and photocatalytic properties were studied. DA was dissolved in tetrahydrofuran (THF) and mixed with an acidified aqueous solution containing chitosan to obtain chitosan/DA (CS/DA) films by solution casting. The fabricated biobased films were characterized using spectroscopic techniques (FT-IR and UV-vis), thermogravimetry, mechanical assays, contact angle analysis, and atomic force microscopy (AFM). The effects of varying DA compositions and the results of exposure to visible-light irradiation of the films were also analyzed. The results indicated the existence of interactions between chitosan and DA and a potentially profitable light-driven response of these biobased films. This behavior was reflected in the optical, topographical, and contact angle properties of the films, which exhibited different characteristics before and after visible-light exposure. Finally, the photocatalytic performance of the biobased films was tested via the decomposition of methyl orange (MO), as a reaction model system. Our results revealed a significant photocatalytic activity (according to biobased film composition, approximately 64 % and 87 % of methyl orange were degraded under continuous visible-light irradiation for 120 min) of the films which is attributed to the combined presence and synergetic effects of the film-forming ability of chitosan and the photoproperties of DA.The objective of this work was to extract, identify and characterize a galactose-rich heteropolysaccharide (GH) from "jaboticaba" peel. The best conditions to extract the GH according to a 23 full-factorial experimental design were 90 °C/30 min/pH 1.0, resulting in a 32.32 % yield using lyophilized sample. The chemical structure analyzed by GC/MS and NMR spectra (HSQC/HSQC-TOCSY) showed that the main chain of GH consists of a (1→4) galactoside branched at carbon 3, containing galactose (67.21 %), glucose (15.78 %), arabinose (9.78 %), rhamnose (2.26 %) and traces of esterified and non-esterified uronic acids. Rheological studies revealed that GH suspensions behave as a Newtonian fluid, with calculated molecular mass of 1.48 × 105 Da. The absolute viscosity of 1 % (w/v) aqueous suspension of GH decreased from 25 mPa s to 10 mPa s in NaCl and 7 mPa s in CaCl2, indicating the polyelectrolyte character of GH.In the current investigation, azidodeoxy-microcrystalline cellulose nitrate (AMCCN) as a novel promising nitrogen-rich energetic biopolymer was synthesized, and its features were compared to those of azidodeoxy-pristine cellulose nitrate (APCN), conventional cellulose nitrate (PCN) and microcrystalline cellulose nitrate (MCCN). The produced nitrated samples and their precursors were fully characterized using various analytical techniques. In addition, the heats of combustion and mechanical sensitivities of all nitrated biopolymers were evaluated, and their energetic performances were predicted by EXPLO5 V6.04 software. The obtained results provide evidence for the effectiveness of the applied chemical functionalization approach to synthesize the relatively insensitive AMCCN and APCN with nitrogen content of 22.75 % and 22.50 %, density of 1.718 g/cm3 and 1.706 g/cm3, and detonation velocity of 7707 m/s and 7533 m/s, respectively, which are higher than those of PCN. This work opens avenues to design promising energetic biopolymers based on renewable microcrystalline cellulose for potential application in advanced high performance solid propellants and explosives.Glycoside hydrolase family 70 (GH70) glucansucrases produce α-d-glucan polysaccharides (e.g. dextran), which have different linkage composition, branching degree and size distribution, and hold potential applications in food, cosmetic and medicine industry. In addition, GH70 branching sucrases add single α-(1→2) or α-(1→3) branches onto dextran, resulting in highly branched polysaccharides with "comb-like" structure. The physico-chemical properties of these α-d-glucans are highly influenced by their linkage compositions, branching degrees and sizes. Among these α-d-glucans, dextran is commercially applied as plasma expander and separation matrix based on extensive studies of its structure and physico-chemical properties. However, such detailed information is lacking for the other type of α-d-glucans. Aiming to stimulate the application of α-d-glucans produced by glucansucrases, we present an overview of the structures, production, physico-chemical properties and (potential) applications of these sucrose-derived α-d-glucan polysaccharides. We also discuss bottlenecks and future perspectives for the application of these α-d-glucan polysaccharides.A polygalactosamino-glucopyranosyl fucopyranose →4)-β-GlcAp(3→1)-α-Fucp-β-GalNAcp-(4,6-SO3-)-(1→ isolated from the bivalve Crassostrea madrasensis exhibited prospective anti-inflammatory activity against cyclooxygenase-2 and 5-lipoxygenase (IC50 less then 50 μg mL-1) on lipopolysaccharide-induced macrophages. The polygalactan attenuated inducible nitric oxide synthase (IC50 65.7 μg mL-1) in lipopolysaccharide-prompted inflammation leading to the reduction of pro-inflammatory cytokine nitric oxide (236.2 μg mL-1 lysate), nuclear factor-κB, tumor necrosis factor-α, and interleukins (0.19-0.22 units mg-1 protein at 100 μg mL-1) by inhibiting cyclooxygenase-2. check details The polygalacatan suppressed the mRNA of nuclear factor-κB and cyclooxygenase-2 in lipopolysaccharide-induced macrophages. Western blot experiment revealed that the polygalactan attenuated the migration of nuclear factor-κB-p65 to the nucleus from cytoplasm, and suppressed the phosphorylation of α-subunit of κB inhibitor. Greater selectivity index of sulfated polygalactan (3.
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