The Effect of Electrospun Gelatin Fibers Alignment on Schwann Cell and Axon Behavior and Organization in the Perspective of Artificial Nerve Design

Electrospun fibrous substrates mimicking extracellular matrices can be prepared by electrospinning, yielding aligned fibrous matrices as internal fillers to manufacture artificial nerves. Gelatin aligned nano-fibers were prepared by electrospinning after tuning the collector rotation speed. The effect of alignment on cell adhesion and proliferation was tested in vitro using primary cultures, the Schwann cell line, RT4-D6P2T, and the sensory neuron-like cell line, 50B11. Cell adhesion and proliferation were assessed by quantifying at several time-points. Aligned nano-fibers reduced adhesion and proliferation rate compared with random fibers. Schwann cell morphology and organization were investigated by immunostaining of the cytoskeleton. Cells were elongated with their longitudinal body parallel to the aligned fibers. B5011 neuron-like cells were aligned and had parallel axon growth when cultured on the aligned gelatin fibers. The data show that the alignment of electrospun gelatin fibers can modulate Schwann cells and axon organization in vitro, suggesting that this substrate shows promise as an internal filler for the design of artificial nerves for peripheral nerve reconstruction.     

A Critical Review of Biological Processes and Technologies for Landfill Leachate Treatment

The most common method to deal with the huge production of municipal wastes is still the disposal in landfills which, however, generates a leachate with high contents of organic and nitrogen pollutants. Requirements must be fixed by law to control leachate release from such landfills, and effective treatment processes and technologies must be applied to reduce its impact on the environment. Biological processes for leachate treatment are discussed in this review, in the former part of which attention is paid to leachate formation and its qualitative and quantitative features, while the latter deals with the state‐of‐the‐art of the most effective biotechnological treatments presently employed. Processes, alternative methods, and technological improvements are compared, with special focus on novel technologies to remove nitrogen pollutants from leachate, highlighting advantages and drawbacks of each treatment.     

Oxidative Stress in Obesity: A Critical Component in Human Diseases

Obesity, a social problem worldwide, is characterized by an increase in body weight that results in excessive fat accumulation. Obesity is a major cause of morbidity and mortality and leads to several diseases, including metabolic syndrome, diabetes mellitus, cardiovascular, fatty liver diseases, and cancer. Growing evidence allows us to understand the critical role of adipose tissue in controlling the physic-pathological mechanisms of obesity and related comorbidities. Recently, adipose tissue, especially in the visceral compartment, has been considered not only as a simple energy depository tissue, but also as an active endocrine organ releasing a variety of biologically active molecules known as adipocytokines or adipokines. Based on the complex interplay between adipokines, obesity is also characterized by chronic low grade inflammation with permanently increased oxidative stress (OS). Over-expression of oxidative stress damages cellular structures together with under-production of anti-oxidant mechanisms, leading to the development of obesity-related complications. The aim of this review is to summarize what is known in the relationship between OS in obesity and obesity-related diseases.     

A novel consolidation method to measure powder flow properties using a small amount of material

Bulk flow property characterization often requires large powder samples (tens to hundreds of grams). However, many applications have limited sample availability, due to cost, material availability, safety concerns, etc. Therefore, reducing the amount of required material is of interest. A novel compressibility method is introduced using less than 50 mg, for the materials studied here. The effect of particle size and cohesion due to capillary forces are determined using a small‐scale compressibility cell mounted on a texture analyzer. It is found that the powder bed consolidation occurred in two regimes, described using the Walker and Heckel equations. The small‐scale compressibility method was compared to known behavior at larger scales and validated against the FT4 compressibility test. It was found that bulk behavior could be observed using the small‐scale compressibility method. Additional behavior caused by small‐scale events, which are averaged out in large‐scale measurements, are revealed in the small‐scale device introduced here. © 2016 American Institute of Chemical Engineers AIChE J, 62: 4193–4200, 2016     

Dynamics and Selectivity of N<Subscript>2</Subscript>O Formation/Reduction During Regeneration Phase of Pt-Based Catalysts

The formation of N₂O has been studied by means of isothermal lean-rich experiments at 150, 180 and 250 °C over Pt–Ba/Al₂O₃ and Pt/Al₂O₃ catalysts with H₂ and/or C₃H₆ as reductants. This allows to provide further insights on the mechanistic aspects of N₂O formation and on the influence of the storage component. Both gas phase analysis and surface species studies by operando FT-IR spectroscopy were performed. N₂O evolution is observed at both lean-to-rich (primary N₂O) and rich-to-lean (secondary N₂O) transitions. The production of both primary and secondary N₂O decreases by increasing the temperature. The presence of Ba markedly decreases secondary N₂O formation. FT-IR analysis shows the presence of adsorbed ammonia at the end of the rich phase only for Pt/Al₂O₃ catalyst. These results suggest that: (i) primary N₂O is formed when undissociated NO in the gas phase and partially reduced metal sites are present; (ii) secondary N₂O originates from reaction between adsorbed NH₃ and residual NO_x at the beginning of the lean phase. Moreover, N₂O reduction was studied performing temperature programming temperature experiments with H₂, NH₃ and C₃H₆ as reducing agents. The reduction is completely selective to nitrogen and occurs at temperature higher than 250 °C in the case of Pt–Ba/Al₂O₃ catalyst, while lower temperatures are detected for Pt/Al₂O₃ catalyst. The reactivity order of the reductants is the same for the two catalysts, being hydrogen the more efficient and propylene the less one. Having H₂ a high reactivity in the reduction of N₂O, it could react with N₂O when the regeneration front is developing. Moreover, also ammonia present downstream to the H₂ front could react with N₂O, even if the reaction with stored NO_x seems more efficient.     

A novel polymer‐based genosensor for the detection and quantification of Streptococcus pneumoniae in genomic DNA sample

The Streptococcus pneumoniae detection plays an important role in the diagnosis and monitoring of pneumococcal diseases. A genosensor based on graphite electrodes modified with polymer was developed for such detection. First, the poly(4‐aminophenol) film was electrochemically deposited on a graphite electrode. Afterward, an S. pneumoniae‐specific oligonucleotide (Strep1), isolated from conserved regions of the bacterial genome, was immobilized onto the modified electrode surface and used for the test with complementary target oligonucleotide (Strep2) or genomic DNA. The genosensor was evaluated using electrochemical techniques and atomic force microscopy. Poly(4‐aminophenol) film caused an increase in probe immobilization, monitoring the guanine oxidation peak. The detection limits obtained using differential pulse voltammetry and electrochemical spectroscopy impedance were 54 and 28 ng mL^?1, respectively. The novel genosensor was efficient for the immobilization and detection of S. pneumoniae genomic DNA. POLYM. ENG. SCI., 58:1308–1314, 2018. © 2017 Society of Plastics Engineers     

Influence of Reaction Conditions on Diacid Formation During Au-Catalyzed Oxidation of Glycerol and Hydroxymethylfurfural

The selective oxidation of glycerol and 5-hydroxymethylfurfural (HMF) to diacids over supported gold catalysts (Au/C and Au/TiO₂) in liquid water at mild temperatures was a strong function of the added base such as NaOH. Use of hydrotalcite as a solid base in place of NaOH in the HMF reaction medium facilitated the production of diacid over Au/TiO₂, but extensive leaching of magnesium suggested that hydrotalcite was consumed stoichiometrically in the reaction. Production of diacids from glycerol oxidation over supported Au catalysts was promoted by operating in a continuous flow reactor and by increasing the catalyst loading in a semi-batch reactor. Trace inhibitors formed by conversion of the product monoacid are proposed to account for the generally low selectivity to diacids over gold catalysts.     

Selective hydrogenation of cinnamaldehyde using Pd catalysts supported on Mg/Al mixed oxides: Influence of the Pd incorporation method

A series of hydrotalcite‐like compounds was synthesized by varying Mg/Al molar ratio with values of 2, 3, and 4. After thermal treatment at 823 K, the corresponding mixed oxides were obtained and used as catalytic supports. The incorporation of a Pd metallic phase (0.5 g/g loading), was carried out by two methods: 1) in situ vapour phase thermal decomposition, and 2) impregnation by organic method. Fresh and calcined samples were characterized by XRD and N₂ sorption experiments. The basic and metal functions were analyzed by CO₂‐TPD and H₂‐TPR. The Pd‐support interaction was studied by FTIR spectroscopy using CO as a probe molecule while the morphology of Pd nanoparticles on the catalysts was studied by SEM, HRTEM, and theoretical simulation using the Fast Fourier Transform (FFT) method. Finally, the catalytic activity results showed a higher conversion towards hydrocinnamaldehyde in the cinnamaldehyde hydrogenation reaction for the catalysts prepared by vapour phase thermal decomposition, compared with those prepared by organic method, showing the significant dependence on the catalytic activity and the Pd incorporation method.     

Microstructural and microwave dielectric properties of LZT (Li2ZnTi3O8) ceramics sintered in presence of bismuth borate glass for LTCC applications

In the present research, the Li₂ZnTi₃O₈(LZT) ceramics were synthesized throughout solid-state ceramic processing, then mixed with bismuth borate (BiBO) glass prepared based on conventional melt quenching method. Wetting behavior of BiBO glass on the LZT ceramic substrate was monitored by hot stage microscopy. Afterward, dielectric LZT ceramics containing different amounts of BiBO glass (0.25–6 wt%) were sintered at various temperatures. X-ray diffraction and electron back scatter diffraction examinations revealed the presence of two crystalline phases of Li₂ZnTi₃O₈ and Bi₂Ti₂O₇. The maximum value of relative density (above 95%) was obtained in the case of specimens contained more than 5 wt% glass. The microwave dielectric properties of the finally sintered BiBO glass containing LZT ceramics were as follows: dielectric constant (ε_r) = 21.44–25.09, quality factor (Q × f) = 10839–54708 GHz and temperature coefficient of resonant frequency (τ_f) = (? 15.58) ? (? 12.86)ppm/°C.