3% ASKG addition. On the other hand, the higher levels of gum substitution at 0.5% and 0.8% tended to disrupt this stronger network with visible signs of starch deformation, due to the inefficient entrapment of starch molecules during cooking as a result of the lack of gluten network. Magnetic graphene quantum dots were prepared and incorporated in cyclodextrin decorated chitosan. The resulting hybrid was then palladated and characterized using TEM, BET, TGA, XRD, VSM, ICP and FTIR spectroscopy. Next, the catalytic activity of the prepared hybrid catalyst that benefits from the chemistry of both carbohydrates and magnetic graphene quantum dots was investigated for promoting hydrogenation reaction of nitroarenes in aqueous media under mild reaction condition. The study of the catalyst performance confirmed high catalytic activity and selectivity of the catalyst towards hydrogenation of the nitro group. Moreover, the catalyst could be magnetically separated from the reaction mixture and recycled up to ten reaction runs with a slight loss of the catalytic activity and Pd leaching. These results showed that the hybrid of magnetic graphene quantum dots and carbohydrates is an efficient catalyst support that can be potentially applied for the immobilization of nanoparticles to furnish heterogeneous catalysts for promoting the chemical transformations. V.The aim of the present study was to use microencapsulation technologies to create microcapsules containing polyphenol extracted from maca leaves, which were coated with maltodextrin (MD) and neutral polysaccharides extracted from maca roots (NPMR). NPMR was composed of arabinose, galactose, rhamnose, and glucose, with the main linkage types of →5)-α-L-Araf-(1→, →2,5)-α-L-Araf-(1→, α-L-Araf-(1→, →3)-β-D-Galp-(1→, and β-D-Rhap-(1→. The microencapsulation efficiency of the powdered microcapsules increased with an increasing MP concentration in the coating materials. SEM images showed that, according to the increase in the MP concentration, the powdered microcapsules were more spherical and smoother, with a smaller particle size. The polyphenols extracted from the maca leaves were successfully microencapsulated in an MD-NPMR coat, as confirmed by FT-IR spectra analysis. The storage stability was greater at several temperatures for the powdered microcapsules coated with MD-MP than for those of the microcapsules coated with only MD. In an in vitro study, the powdered microcapsules coated with MD-NPMR released a smaller amount of polyphenol than the microcapsules coated with only MD in simulated gastric and intestinal fluids. Furthermore, the powdered microcapsules coated with MD-NPMR produced greater Bifidobacterium longum probiotic growth than did the microcapsules coated only with MD. Thymol is the major antimicrobial and bioactive constituent found in thyme (Thymus vulgaris) essential oil. https://www.selleckchem.com/products/ag-221-enasidenib.html In this study, it was aimed to determine the parameters for fabrication of thymol loaded chitosan nanoparticles with optimum encapsulation efficiency, zeta potential, and particle size properties using a two-stage emulsion-ionic gelation approach. For this purpose, temperature (25-45 °C) and chitosan (3-6 mg/mL), thymol (3-6 mg/mL), Tween 80 (3-6 mg/mL) and TPP (0.15-0.75 mg/mL) concentrations were studied as optimization parameters by applying the numerical point prediction method. The results showed that the particle size, zeta potential and encapsulation efficiency of the chitosan nanoparticles could be controlled by processing conditions. Additionally, this study was focused on optimization of these parameters with factorial design (FD) in nanoencapsulation of Thymol. The optimized production parameters on the basis of the criteria of attaining the minimum particle size, maximum zeta potential, and maximum encapsulation efficiency were 42 °C temperature, chitosan rate 3 mg/mL, Thymol rate 5.9 mg/mL, Tween 80 rate 3 mg/mL and TPP rate 0.75 mg/mL. In this study, a class of interpenetrating network (IPN) gels were successfully fabricated based on glucono-δ-lactone (GDL) induced gelation of mixed alginate (Alg) and deacylated gellan (gellan) systems. The IPN gels were prepared by co-hydrating a mixed Alg and gellan powder, followed by adding GDL and calcium carbonate (CaCO3) in sequence to initiate the gelation. It was found that Alg and gellan can form independently a gel network, with no significant interaction between the two types of gel networks observed, as indicated by the results of gel strength determination, scanning electron microscope (SEM) observations and thermogravimetry (TG) and derivative thermogravimetric (DTG) analyses. Moreover, the mixing ratio of Alg to gellan significantly affected the physical properties of the fabricated gels. With increasing Alg to gellan ratio, the gels tended to become more elastic, and to show a higher rehydration rate and rehydration extent. Overall, these tunable properties may allow the fabricated gels to find potential applications in designing or optimizing the structures of gel-related food products. Here, non-invasive and label-free detection of trace-level of norfloxacin (NF) in human urine samples has been reported using the electrochemical technique. Nanostructured yttrium oxide (nY2O3) was synthesized at low-temperature using a one-step hydrothermal process. These nY2O3 were characterized by various methods including XRD, FT-IR, Raman spectroscopy, and TEM. A biosensing platform based on nY2O3 modified with chitosan (CH) was fabricated for the detection of NF. The nanocomposite film (CH-Y2O3/ITO) was characterized by FE-SEM, contact angle measurements, and electrochemical techniques. Further, fluoroquinolones antibodies (anti-FQ) were used to modify the CH-Y2O3/ITO electrode via covalent interaction. Non-specific sites were blocked by bovine serum albumin (BSA), those present on the anti-FQ/CH-Y2O3/ITO electrode surface. The response study of BSA/anti-FQ/CH-Y2O3/ITO bioelectrode towards NF detection revealed a wide range (1 pM-10 μM) with a lower detection limit of 3.87 pM using differential pulse voltammetry (DPV). The sensitivity obtained is as high as 10.14 μA μM-1 cm2 with a fast response time of ~10 min. Moreover, the diagnostic performance of the fabricated sensor was evaluated to detect NF in urine spiked sample. The recovery of NF from the spiked sample was observed from 90.5 to 101.1%, with a maximum relative standard deviation of 7.04. The obtained results of the fabricated bioelectrode (BSA/anti-FQ/CH-Y2O3/ITO) was validated with ELISA. The results were found better when compared with earlier described biosensors and commercially existing ELISA in terms of sensitivity and lower detection limit.