Electrochemical and thermal properties of SmBa0.5Sr0.5Co2O5+δ cathode impregnated with Ce0.8Sm0.2O1.9 nanoparticles for intermediate-temperature solid oxide fuel cells

SmBa_0.5Sr_0.5Co₂O_5+δ (SBSC55) impregnated with nano-sized Ce_0.8Sm_0.2O_1.9 (SDC) powder has been investigated as a candidate cathode for intermediate-temperature solid oxide fuel cells (IT-SOFCs). The cathode chemical compatibility with electrolyte, thermal expansion behavior, and electrochemical performance are investigated. For compatibility, a good chemical compatibility between SBSC55 and SDC electrolyte is still kept at 1100 °C in air. For thermal dilation curve, it could be divided into two regions, one is the low temperature region (100–265 °C); the other is the high temperature region (265–850 °C). In the low temperature region (100–265 °C), a TEC value is about 17.0 × 10^?6 K^?1 and an increase in slope in the higher temperatures region (265–800 °C), in which a TEC value is around 21.1 × 10^?6 K^?1. There is an inflection region ranged from 225 to 330 °C in the curve of d(δL/L)/dT vs. temperature. The peak inflection point located about 265 °C is associated to the initial temperature for the loss of lattice oxygen and the formation of oxygen vacancies. For electrochemical properties, the polarization resistances (R_p) significantly reduced from 4.17 Ω cm² of pure SBSC55 to 1.28 Ω cm² of 0.65 mg cm^?2 of SDC-impregnated SBSC55 at 600 °C. The single cell performance of SBSC55∣SDC∣Ni-SDC loaded with 0.65 mg cm^?2 SDC exhibited the optimum power density of 823 mW cm^?2 at operating temperature of 800 °C. Based on above-mentioned properties, SBSC55 impregnated with an appropriate SDC is a potential cathode for IT-SOFCs.     

Performance Comparison of Five Methods for Tetrahymena Number Counting on the ImageJ Platform: Assessing the Built-in Tool and Machine-Learning-Based Extension

Previous methods to measure protozoan numbers mostly rely on manual counting, which suffers from high variation and poor efficiency. Although advanced counting devices are available, the specialized and usually expensive machinery precludes their prevalent utilization in the regular laboratory routine. In this study, we established the ImageJ-based workflow to quantify ciliate numbers in a high-throughput manner. We conducted Tetrahymena number measurement using five different methods: particle analyzer method (PAM), find maxima method (FMM), trainable WEKA segmentation method (TWS), watershed segmentation method (WSM) and StarDist method (SDM), and compared their results with the data obtained from the manual counting. Among the five methods tested, all of them could yield decent results, but the deep-learning-based SDM displayed the best performance for Tetrahymena cell counting. The optimized methods reported in this paper provide scientists with a convenient tool to perform cell counting for Tetrahymena ecotoxicity assessment.     

Rlip76: An Unexplored Player in Neurodegeneration and Alzheimer’s Disease?

Alzheimer’s disease (AD) is a progressive neurodegenerative disorder and is the most common cause of dementia in older people. AD is associated with the loss of synapses, oxidative stress, mitochondrial structural and functional abnormalities, microRNA deregulation, inflammatory responses, neuronal loss, accumulation of amyloid-beta (Aβ) and phosphorylated tau (p-tau). AD occurs in two forms: early onset, familial AD and late-onset, sporadic AD. Causal factors are still unknown for a vast majority of AD patients. Genetic polymorphisms are proposed to contribute to late-onset AD via age-dependent increases in oxidative stress and mitochondrial abnormalities. Recent research from our lab revealed that reduced levels of Rlip76 induce oxidative stress, mitochondrial dysfunction and synaptic damage, leading to molecular and behavioral phenotypes resembling late-onset AD. Rlip76 is a multifunctional 76 kDa protein encoded by the RALBP1 gene, located on chromosome 18. Rlip is a stress-protective ATPase of the mercapturic acid pathway that couples clathrin-dependent endocytosis with the efflux of glutathione–electrophile conjugates. Rlip is evolutionarily highly conserved across species and is ubiquitously expressed in all tissues, including AD-affected brain regions, the cerebral cortex and hippocampus, where highly active neuronal metabolisms render the cells highly susceptible to intracellular oxidative damage. In the current article, we summarize molecular and cellular features of Rlip and how depleted Rlip may exacerbate oxidative stress, mitochondrial dysfunction and synaptic damage in AD. We also discuss the possible role of Rlip in aspects of learning and memory via axonal growth, dendritic remodeling, and receptor regulation. We conclude with a discussion of the potential for the contribution of genetic polymorphisms in Rlip to AD progression and the potential for Rlip-based therapies.     

Sera of Neuromyelitis Optica Patients Increase BID-Mediated Apoptosis in Astrocytes

Neuromyelitis optica (NMO) is a rare disease usually presenting with bilateral or unilateral optic neuritis with simultaneous or sequential transverse myelitis. Autoantibodies directed against aquaporin-4 (AQP4-IgG) are found in most patients. They are believed to cross the blood–brain barrier, target astrocytes, activate complement, and eventually lead to astrocyte destruction, demyelination, and axonal damage. However, it is still not clear what the primary pathological event is. We hypothesize that the interaction of AQP4-IgG and astrocytes leads to DNA damage and apoptosis. We studied the effect of sera from seropositive NMO patients and healthy controls (HCs) on astrocytes’ immune gene expression and viability. We found that sera from seropositive NMO patients led to higher expression of apoptosis-related genes, including BH3-interacting domain death agonist (BID), which is the most significant differentiating gene (p < 0.0001), and triggered more apoptosis in astrocytes compared to sera from HCs. Furthermore, NMO sera increased DNA damage and led to a higher expression of immunological genes that interact with BID (TLR4 and NOD-1). Our findings suggest that sera of seropositive NMO patients might cause astrocytic DNA damage and apoptosis. It may be one of the mechanisms implicated in the primary pathological event in NMO and provide new avenues for therapeutic intervention.     

The Effects of Antioxidants from Natural Products on Obesity,Dyslipidemia, Diabetes and Their Molecular Signaling Mechanism

Obesity is a risk factor that leads to the development of other diseases such as dyslipidemia and diabetes. These three metabolic disorders can occur simultaneously, hence, the treatment requires many drugs. Antioxidant compounds have been reported to have activities against obesity, dyslipidemia and diabetes via several mechanisms. This review aims to discuss the antioxidant compounds that have activity against obesity, dyslipidemia and diabetes together with their molecular signaling mechanism. The literature discussed in this review was obtained from the PUBMED database. Based on the collection of literature obtained, antioxidant compounds having activity against the three disorders (obesity, dyslipidemia and diabetes) were identified. The activity is supported by various molecular signaling pathways that are influenced by these antioxidant compounds, further study of which would be useful in predicting drug targets for a more optimal effect. This review provides insights on utilizing one of these antioxidant compounds as opposed to several drugs. It is hoped that in the future, the number of drugs in treating obesity, dyslipidemia and diabetes altogether can be minimized consequently reducing the risk of side effects.     

Degradation of 1,1,1-trichloro-2,2-bis (4-chlorophenyl) ethane (DDT) by brown-rot fungi

Twelve species of brown-rot fungi (BRF) have been investigated for their ability to degrade 1,1,1-trichloro-2,2-bis (4-chlorophenyl) ethane (DDT). In potato dextrose broth (PDB) medium, Gloeophyllum trabeum, Fomitopsis pinicola and Daedalea dickinsii showed a high ability to degrade DDT. 1,1-Dichloro-2,2-bis (4-chlorophenyl) ethane (DDD), 1,1-dichloro-2,2-bis (4-chlorophenyl) ethylene (DDE) and 4,4-dichlorobenzophenone (DBP) were detected as metabolic products of DDT degradation by G. trabeum in PDB medium. The DDT degradation pathway in G. trabeum is proposed, which differs from the proposed pathways in bacteria and other fungi, particularly in the transformation of DDE to DDD. On the other hand, DBP was not detected as a metabolic product of DDT degradation in FeSO(4)-deficient cultures of G. trabeum, whereas DDE and DDD were detected, indicating the involvement of an iron-dependent reaction. Only DBP was detected from DDT, DDE and DDD degradation via a chemical Fenton reaction under conditions similar to those in G. trabeum cultures. These compounds may be directly transformed to DBP via a Fenton reaction.     

The Evolution of Tumor-Targeted Drug Delivery: From the EPR Effect to Nanoswimmers

Therapeutic nanotechnologies have made great progress over the past decade. Skepticism has been replaced by the understanding that precision at the nanoscale allows improved treatment modalities in humans. Principles for designing tumor-targeted drug delivery systems are described. At first, the enhanced permeability and retention (EPR) effect was the major targeting mode, with up to 10 % of the injected dose actually reaching tumors. To improve cellular uptake, sugars, antibodies, peptides or other ligands were added to the surface of nanotherapeutics. These can be coupled with external magnetic fields or ultrasonic waves to propel iron oxide or gas-filled particles towards the disease site. Next-generation drug delivery systems will be capable of autonomously swimming towards the disease site and penetrating deep tissue, independent of blood or lymphatic flow. This has been shown to some extent with modified, drug-producing, bacteria. Interestingly, sperm may be nature’s best example of a multifunctional, targeted, high-fidelity, self-propelled, delivery system that we can learn from.     

Silane-Modified Graphene Oxide as a Compatibilizer and Reinforcing Nanoparticle for Immiscible PP/PA Blends

Graphene oxide (GO) and aminosilane (AS)-modified GO (GOAS) have been studied as possible compatibilizers for immiscible polyblends. Ideally, for localization of nanoparticles (NPs) at the interface, the thermodynamics of the constituents and mixing dynamics have to be tailored and controlled, respectively. Accordingly, a variety of oxidation levels (10%–40%) of GOs were prepared using Hummer's method and further modified by AS. Experimental results indicated that the GO goes through thermal reduction (above 200°C) during blending and reduced GO (rGO) is produced. The GOAS moderated the reduction reaction and stabilized the GO. The thermodynamic wetting coefficient of PP (polypropylene)/PA (polyamide)/rGOAS system was shown to drive the rGOAS from the PP phase to the blend's interface during time-controlled blending. The localization of the rGOAS at the interface resulted in significant enhancement of mechanical properties using only 2–3 wt% of rGOAS. Over 100% enhancement in strength, 40% enhancement in modulus, and 30% in toughness were shown, compared with neat PP/PA. Reduced GOAS and its location at the interface resulted in a third glass transition temperature (Tg), in addition to the PP and PA respective Tgs. Rheological percolation at 2–3 wt% rGOAS (20%) supports the localization of rGOAS at the interface. Storage moduli increase with interfacial tension, in accordance to the rheological models. POLYM. ENG. SCI., 60:180–191, 2020. © 2019 Society of Plastics Engineers