Ozone based food preservation: a promising green technology for enhanced food safety

Extending shelf life of food products is a major concern of the producers, and the food industry requires ‘greener’ alternatives to the current technologies. Ozone-based food preservation may suit this niche. Ozone is an attractive alternative preservative that food industry needs due to its properties such as quick decomposition and little residual effect during food preservation. Ozone is the strongest molecule available for the disinfection of water and is second only to elemental fluorine in oxidizing power. Ozone is being used in the food industry in various applications such as decontamination of water and equipment surfaces. Several researchers have focused on the application of ozone to inactivate microorganisms on fresh produce, like fruits, vegetables, meat, poultry, fish, and eggs, and dry produce, such as cereals, pulses, and spices. This review comprehensively analyses appropriate ozone concentrations and exposure times and discusses various factors that affect the quality and safety of food products during ozonation.     

Mangiferin Inhibits Apoptosis in Doxorubicin-Induced Vascular Endothelial Cells via the Nrf2 Signaling Pathway

Doxorubicin increases endothelial permeability, hence increasing cardiomyocytes’ exposure to doxorubicin (DOX) and exposing myocytes to more immediate damage. Reactive oxygen species are major effector molecules of doxorubicin’s activity. Mangiferin (MGN) is a xanthone derivative that consists of C-glucosylxanthone with additional antioxidant properties. This particular study assessed the effects of MGN on DOX-induced cytotoxicity in human umbilical vein endothelial cells’ (HUVECs’) signaling networks. Mechanistically, MGN dramatically elevated Nrf2 expression at both the messenger RNA and protein levels through the upregulation of the PI3K/AKT pathway, leading to an increase in Nrf2-downstream genes. Cell apoptosis was assessed with a caspase-3 activity assay, transferase-mediated dUTP-fluorescein nick end labeling (TUNEL) staining was performed to assess DNA fragmentation, and protein expression was determined by Western blot analysis. DOX markedly increased the generation of reactive oxygen species, PARP, caspase-3, and TUNEL-positive cell numbers, but reduced the expression of Bcl-2 and antioxidants’ intracellular concentrations. These were effectively antagonized with MGN (20 μM), which led to HUVECs being protected against DOX-induced apoptosis, partly through the PI3K/AKT-mediated NRF2/HO-1 signaling pathway, which could theoretically protect the vessels from severe DOX toxicity.     

Enhanced photocatalytic performance of CuFeO2-ZnO heterostructures for methylene blue degradation under sunlight

One of the strategies to overcome the drawbacks of fast charge recombination of a photocatalyst is to develop semiconductor heterostructures. Herein, we report a two-step precipitation-hydrothermal process to create CuFeO₂-ZnO heterostructures with different weight percentages of CuFeO₂ (0.5, 1, 5, and 10%). Though X-ray diffraction detected the presence of CuFeO₂ on ZnO above 5%, Raman spectroscopy could reveal the presence of CuFeO₂ phase as low as 0.5 wt%. For all of the compositions, the bandgap of ZnO did not vary (3.15 eV) on forming heterostructures with CuFeO₂. The oxidation of methylene blue under sunlight was used to determine the photocatalytic performance of the heterostructures. In comparison to pure ZnO and CuFeO₂, CuFeO₂-ZnO heterostructures exhibited a better photocatalytic efficiency. Overall, 5 wt% CuFeO₂ on ZnO showed 100% degradation with a rate constant of 0.272?±?0.002 min^?1, which is 16 times faster than ZnO. Time-resolved photoluminescence analysis indicated a higher lifespan of charge carriers in the 5wt% CuFeO₂-ZnO heterostructure (32.3 ns) than that of CuFeO₂ (0.85 ns) and ZnO (27.6 ns). The Mott–Schottky flat band potentials of ZnO and CuFeO₂ was determined to be -0.82 and 1.17 eV, respectively, revealing the presence of Type I heterostructures. The heterostructures also showed outstanding recyclability, with a degradation rate of 97% even after four cycles. The current study shows the significance of forming p-type CuFeO₂ and n-type ZnO heterostructures for enhanced photocatalysis.

     

Structural and optical absorption studies of cobalt substituted strontium ferrites,SrCo<Subscript>x</Subscript>Fe<Subscript>12−x</Subscript>O<Subscript>19</Subscript> (x = 0.1, 0.2 and 0.3)

Cobalt substituted strontium ferrites SrCo_xFe_12?xO₁₉ (x = 0.1, 0.2 and 0.3) were synthesized via sol–gel method and the dried gel obtained was annealed at 800 °C. The powder X-ray diffraction studies helped in the determination of the crystallite size that measured ≈ 12–14 nm. The optical properties of the powdered nanoparticles were determined by means of the UV–Vis absorption spectra of their dispersed solutions in liquid media. Despite these measurements, it was difficult to determine their band gap (E_g) precisely. However, the Kubelka–Munk treatment on the diffuse reflectance spectra of the powdered nanoparticles was used in order to extract their E_g unambiguously. The Co substituted strontium hexaferrites are used for optical studies. The energy band gap for all the ferrite compositions was found to be ≈ 1.46–1.78 eV. The study made on the dielectric behaviour of the substituted SrFe₁₂O₁₉ is also discussed in this paper.     

Structural,electrical and magnetic properties of Mn<Subscript>3</Subscript>O<Subscript>4</Subscript>/MgO nanocomposite

The present paper deals with the synthesis of Mn₃O₄/MgO nanocomposite through a simple sol–gel route and their electrical and magnetic properties are discussed for electrode applications. The grain size and particle morphology of the synthesized nanocomposite are characterized using XRD and HRSEM. The elemental compositions of the synthesized samples were analyzed using EDAX spectra. The dielectric constant, dielectric loss and AC conductivity of the synthesized samples were studied in the frequency range of 100 Hz–5 MHz at different temperatures (303–573 K) using impedance spectra. The activation energy was calculated using Arrhenius plot. The vibrating sample magnetometry (VSM) study shows that the nanocomposites are found to be paramagnetic at room temperature.     

Optical and electrical smart response of chemically stabilized graphene oxide

Graphene oxide (GO) was prepared using a modified Hammer’s technique and by utilizing a sonochemical approach. The paper deals with the synthesis and the characterization of GO besides the structural, morphological, optical and electrical properties of GO. Phase formation of the prepared sample was examined with powder X-ray diffraction (XRD), the typical surface morphology was carried out by utilizing Scanning electron microscopy (SEM) and the high resolution Transmission Electron Microscopy (HR-TEM). The different functional groups were recognized by utilizing FT-IR and Raman spectroscopy. The optical properties were studied utilizing optical absorption and photoluminescence (PL) spectra. At various frequencies and temperatures the dielectric properties of the GO, such as the dielectric constant, the dielectric loss, and AC conductivity were studied. Further, the electrical behaviour of GO was analysed using I-V and C-V characteristics. These novel findings shed focus on high yield electronic material GO, which can only be realized as the field moves forward and makes more significant advances in smart opto-electronic devices.     

Investigation of in vitro permeability and in vivo pharmacokinetic behavior of bare and functionalized MCM-41 and MCM-48 mesoporous silica nanoparticles: a burst and controlled drug release system for raloxifene

In the present work, MCM-41 and MCM-48 type of nanoparticles were successfully engineered. Effect of nanosize and amine functionalization on drug release, in vitro intestinal absorption and in vivo pharmacokinetic behavior was investigated in a comprehensive manner. The tailor-made bare and surface decorated MCM-41 and MCM-48 were synthesized and evaluated for their mesoporous skeleton, pore size, particle size, surface area, zeta potential, etc. by nitrogen sorption, DLS, TEM, etc. Incorporation of raloxifene (RLF) was affirmed using optimized immersion-solvent evaporation technique and its success confirmed by DSC, IR, and XRD analysis. TGA analysis revealed higher %grafting of amine groups on the exterior and larger RLF encapsulation into mesoporous derivate. The detailed in vitro release study revealed SGF to be the most compatible media for RLF showing an initial burst release from pristine nanoparticles and a delayed release from surface coated nanoparticles. Furthermore, release kinetics model data demonstrated Weibull and Higuchi as the best fit models for bare and amine-functionalized nanoparticles respectively. Moreover, an in vitro permeability study on Caco-2 cell line revealed higher absorption by engineered nanoparticle as compared to pure RLF and its marketed formulation. The supremacy in the in vivo pharmacokinetic parameters of RLF-41 and RLF-48 was demonstrated with 3.33 and 3.50 times enhancement in the bioavailability of RLF with respect to RLF suspension. To sum up, the results obtained were superior and promising for synthesized nanoparticles and more precisely for MCM-48 amongst them.     

A pilot level approach to remove anionic species from industrial effluents using a novel carbonate-steam pyrolysed activated charcoal system

In our laboratory, we synthesized a novel surface tailored activated charcoal in removing nitrite species from fertilizer industrial effluents. A customized high temperature carbonate-steam activation technique was adopted to develop the sodium carbonate impregnated activated charcoal (SCIAC). The surface properties of the material were determined using SEM, TG and X-RD techniques. Batch adsorption experiments were performed for optimizing various conditions such as solution pH, contact time, temperature and adsorbent dose for maximizing the nitrite adsorption onto SCIAC. Considerably, a very high nitrite adsorption percentage of 83.8 was obtained for an initial nitrite concentration of 5.0?mg/L at pH 3.0. Among the various equilibrium and kinetic models, Freundlich and pseudo-second-order expressions, respectively, were well enough to explain the adsorption processes. In general, it may conclude that the change in surface characteristics of the adsorbent material after the pyrolysis process is highly favorable for effective removal of nitrite ions from aqueous systems. Adsorption capacity of SCIAC was 27.03?mg/g and studies revealed that the material was feasible in removing nitrite from industrial effluents.     

Verifying verified code

Innovations in Systems and Software Engineering - A recent case study from AWS by Chong et al. proposes an effective methodology for Bounded Model Checking in industry. In this paper, we report on...     

A comparison of the determination of macromolecular orientation in polypropylene by attenuated total-reflection fourier-transform infrared spectroscopy and X-ray diffraction

Attenuated total reflection-infrared (ATR-IR) spectroscopy and wide-angle x-ray diffraction (WAXD) were used to determine the macromolecular orientation of a series of six uniaxially oriented polypropylene sheets with elongations of 0% to 500%. The orientation functions were expressed as fractions of chains oriented along the machine, trasverse, and normal directions in the sheets. Good agreement was found between the orientation functions for the two techniques. Sources of potential difference between the two techniques were discussed. The ATR-IR technique is surface sensitive to a depth of about 5 or 10 μm into the surface while the WAXD technique is bulk sensitive. The ATR-IR technique is sensitive to both the crystalline and noncrystalline material while the XRD technique is sensitive only to the crystalline material.