SO2 effect on degradation of MEA and some other amines

AbstractSO2 is the main acidic impurity in flue gas and will affect amine degradation in CO2 capture process. This work introduced SO2/Na2SO3 in various experiment conditions of MEA (monoethanolamine) oxidative degradation and evaluated the SO2 effect on MEA degradation considering both oxidative and thermal degradation. 60ppm SO2 could inhibit MEA oxidative degradation by scavenging oxidative radicals in absorber condition. Higher concentration of SO2 does not enhance the inhibitory effect, but will increase the corrosivity of the solution. NH3 is promoted by sulfite and becomes significant in MEA thermal degradation. Thiosulfate, the disproportionation product of sulfite, is believed to be the catalyst of SN2reaction. Na2SO3 was used to test SO32- effect on thermal degradation of EDA (ethylenediamine), 2-PE (2-piperidineethanol) and PZ/AMP (piperazine/2-amino-2-methyl-1-propanol) solution. Alkyl structure of amines has important effect on the SN2 reactions

Eleutheroside E inhibits doxorubicin-induced inflammation and apoptosis in rat cardiomyocytes by modulating activation of NF-κB pathway

Purpose: To identify the effects of eleutheroside E (EE) on apoptosis and   inflammation induced by doxorubicin (DOX) in H9c2 cells and to investigate the underlying mechanisms.Methods: The effect of EE on H9c2 cell viability was determined using Cell Counting Kit-8 (CCK8). EE effect on DOX-induced apoptosis and inflammation in H9c2 cells was studied by comparison between cells treated with DOX alone and DOX+EE; the relationship between EE effects and NF-κB signaling pathway was evaluated by the addition of NF-κB inhibitor PDTC. Cell apoptosis was examined by flow cytometry while IL-1β, IL-6, and TNF-α levels were determined by ELISA. The phosphorylation level of NF-κB p65 was measured by Western blot.Results: Compared with control group, cell viability was notably elevated after  treatment with 50-100 μM EE for 48 or 72 h. DOX induced higher rates of cell  apoptosis in H9c2 cells (29.5 ± 3.56 %) compared with control group (6.39 ± 0.67 %); however, with EE pretreatment (50 and 80 μM), apoptosis rate decreased to 16.8 ± 2.16 and 13.54 ± 2.08 %, respectively, which are significantly lower than that of DOX group; furthermore, the levels of IL-1β, IL-6, and TNF-α also reduced. In addition, DOX-induced phosphorylation of NF-κB p65 was suppressed by EE pretreatment (10, 50 and 80 μM) to 11.51 ± 1.25, 40.2 ± 5.17 and 52.97 ± 6.74 %, respectivelyConclusion: The results suggest that EE treatment reduced DOX-induced apoptosis and inflammation by interacting with NF-κB signaling pathway. This finding sheds some light on probable new strategies on the application of DOX for cancer treatment.Keywords: Eleutheroside E, Doxorubicin, Inflammation, Apoptosis, Cardiomyocytes, NF-κ

Thermal barrier coatings on polymer materials

Polyimide matrix composite (PIMC) has been widely used to replace metallic parts due to its low density and high strength. It is considered as an effective approach to improve thermal oxidation resistance, operation temperature and lifetime of PIMC by depositing a protection coating. The objective of the research was to fabricate a series of thermal barrier coatings (TBCs) on PIMC by a combined sol-gel/sealing treatment process and air plasma spraying (APS). By optimizing the experimental parameters, thermal shock resistance, thermal oxidation resistance and thermal ablation resistance of PIMC could be improved significantly. The ZrO2 sol was prepared by sol-gel process and the effects of the different organic additions on phase structure, crystallite size and crystal growth behavior of the ZrO2 nanocrystallite were investigated. The addition of HAc and DMF were beneficial to decrease the crystallite size and alter the activation energy for crystal growth, further inducing the crystallization of ZrO2 nanocrystallite at low temperature (300ºC) and the stability of tetragonal ZrO2 at 600ºC. Based on the optimized parameters of the sol preparation, the ZrO2/phosphates duplex coating was fabricated on PIMC via a combined sol-gel and sealing treatment process. The sealing mechanism of the phosphates in the duplex coating was primarily attributed to the adhesive binding of the phosphates and the chemical bonding between the sealant and the coating. It was demonstrated that the duplex coating exhibited excellent thermal shock resistance and no apparent delamination or spallation occurred. Relatively, the duplex coating with the thickness of 150 μm provided excellent thermal oxidation and thermal ablation resistance for the polymer substrate. However, the presence of cracks and delamination in the coatings provided the channels for oxygen diffusion, causing the final failure of the protection coating. Figure 4 – TBCs on CFPI The Zn/YSZ and Al/YSZ coating systems were successfully deposited on PIMC by APS. Metals with comparatively low melting point as the bond coats (Cu, Al, Zn) were beneficial to increase thermal shock resistance of the coating systems. In comparison with the Al/YSZ coating system, the Zn/YSZ coating exhibited the better thermal shock resistance, which was ascribable to the lower residual stress in the Zn layer after deposition and the lower thermal stress induced during thermal shock test. For these coatings, the increase in surface toughness of the substrate as well as the decrease in thickness of metal layer favored the improvement of thermal shock resistance of the coatings. With the temperature increases, thermal shock lifetime of the coatings decreased disastrously. However, the difference was that the slight increase of the thickness of YSZ layer favored the increase in thermal shock resistance of the Al/YSZ coatings, while for the Zn/YSZ coating systems the increase in the thickness of YSZ layer made thermal shock resistance weaken. Owing to the protection of Zn/YSZ and Al/YSZ coating systems, the time for 5 wt% weight loss of the sample was prolonged from 16 h to 50 h when oxidation at 400ºC; as the oxidation temperature increased to 450ºC, the time for 5wt% weight loss was extended from 5 h to 13 h. By depositing different coatings, the anti-ablation property of PIMC was significantly improved. During property testing, the formation of cracks and delamination in the coating and the occurrence of the spallation led to the failure of the coating systems, which was mainly due to the residual stress during the deposition process, thermal stress induced by the mismatch in thermal expansion coefficient and further oxidation of the substrate. Please click Additional Files below to see the full abstract

Correlation between porosity, amorphous phase and CMAS corrosion behaviour of LaMgAl11O19 thermal barrier coatings

Calcium-magnesium-alumino-silicate (CMAS) attack is one of the significant failure mechanisms of thermal barrier coatings (TBCs), which can facilitate TBC’s degradation at elevated temperatures. To clarify the correlation between the porosity, CMAS corrosion behaviour, lanthanum magnesium hexaluminate (LaMgAl11O19, LMA) TBCs were prepared by atmospheric plasma spraying (APS) and then heat-treated at 1173K and 1523K, respectively. For comparison, LMA tablets were prepared by mechanical and cold isostatic pressing. CMAS attack at 1523K was carried out both for LMA tablets and LMA coatings. Their microstructure, phase composition, and crystallization behavior after CMAS attack were investigated using scanning electron microscopy (SEM) equipped with energy dispersive spectroscopy (EDS), X-ray diffraction as well as differential scanning calorimetry (DSC). The results indicated that CMAS attack was arrested for LMA tablets due to the formation of a dense crystalline layer induced by the chemical interactions between LMA and CMAS glass, while the as-sprayed LMA coatings were completely penetrated by molten CMAS due to the presence of amorphous phase and connected pores. Although the isothermal heat-treatment promoted a crystallization of LMA coatings, much vertical cracks formed during heat-treatment. The heat-treated LMA coatings suffered a severer CMAS attack than the as-sprayed one, since the vertical cracks inevitably provided efficient infiltration paths for molten CMAS

Promising Antifungal Targets Against Candida albicans Based on Ion Homeostasis

In recent decades, invasive fungal infections have been increasing significantly, contributing to high incidences and mortality in immunosuppressed patients. Candida albicans (C. albicans) is the most prevalent opportunistic fungal pathogen in humans that can cause severe and often fatal bloodstream infections. Current antifungal agents have several limitations, including that only a small number of classes of antifungals are available, certain of which have severe toxicity and high cost. Moreover, the emergence of drug resistance is a new limitation to successful patient outcomes. Therefore, the development of antifungals with novel targets is an essential strategy for the efficient management of C. albicans infections. It is widely recognized that ion homeostasis is crucial for all living cells. Many studies have identified that ion-signaling and transduction networks are central to fungal survival by regulating gene expression, morphological transition, host invasion, stress response, and drug resistance. Dysregulation of ion homeostasis rapidly mediates cell death, forming the mechanistic basis of a growing number of compounds that elicit antifungal activity. Most of the potent antifungals have been widely used in the clinic, and certain of them have low toxicity, meaning that they may be expected to be used as antifungal drugs in the future. Hence, we briefly summarize the homeostasis regulation of several important ions, potential antifungal targets based on these ion-signaling networks, and antifungal compounds based on the disruption of ion homeostasis. This summary will help in designing effective drugs and identifying new targets for combating fungal diseases

Characterization of the transcripts of human cytomegalovirus UL144

<p>Abstract</p> <p>Background</p> <p>The genome of human cytomegalovirus (HCMV) has been studied extensively, particularly in the UL/b' region. In this study, transcripts of one of the UL/b' genes, UL144, were identified in 3 HCMV isolates obtained from urine samples of congenitally infected infants.</p> <p>Methods</p> <p>Northern blot hybridization, cDNA library screening, and RACE-PCR were used.</p> <p>Results</p> <p>We identified at least 4 differentially regulated 3'-coterminal transcripts of UL144 in infected cells of 1,300, 1,600, 1,700, and 3,500 nucleotides (nt). The 1600 nt transcript was the major form of UL144 mRNA. The largest transcript initiated from the region within the UL141 open reading frame (ORF) and included UL141, UL142, UL143, UL144, and UL145 ORFs.</p> <p>Conclusions</p> <p>These findings reveal the complex nature of the transcription of the UL144 gene in clinical isolates.</p

Comparative Genomic Analysis of Functional Genomics of Lactiplantibacillus plantarum ST

In this study, the functional genomic characteristics of Lactiplantibilus plantarum ST were analyzed. Comparative genomic analysis was performed on the whole genome sequences of L. plantarum ST and the type strain L. plantarum ATCC 14197T as well as those of 152 L. plantarum strains published in the NCBI GenBank. A phylogenetic tree was constructed based on 1 262 core genes of these 154 L. plantarum strains, and the genetic distance between ST and the intestinal isolate BCC9546 was found to be the closest. The isolates originated from milk and meat products were concentrated in the upper part and the lower part of the second branch, respectively, and they were different due to different sources and could be aggregated. Meanwhile, Drosophila isolates showed a significant aggregation trend. Functional annotation analysis suggested that the ST genome contained genes related to the phosphotransferase system (PTS) as a major carbohydrate transport system. Genes related to the immune regulatory pathway were also annotated. There were many genes related to the hydrolysis or rearrangement of glycosidic bonds, but no virulence factors or antibiotics resistance genes found in ST. Compared with the other L. plantarum isolates, ST carried the unique functional gene ecfT related to energy transport function. In addition, ST had functional genes involved in the synthesis of the quorum-sensing signaling molecule AI-2, glutathione, and adhesion molecules. The results of API 50 CHL carbohydrate metabolism showed that L. plantarum ST could utilize a wide range of carbon sources and metabolize 29 carbon sources including monosaccharides, glycosides, disaccharides and polysaccharides. This study provides a genetic basis for the development and utilization of L. plantarum ST as a safe probiotic strain

Anaerobic copper toxicity and iron-sulfur cluster biogenesis in Escherichia coli

© 2017 American Society for Microbiology. While copper is an essential trace element in biology, pollution of groundwater from copper has become a threat to all living organisms. Cellular mechanisms underlying copper toxicity, however, are still not fully understood. Previous studies have shown that iron-sulfur proteins are among the primary targets of copper toxicity in Escherichia coli under aerobic conditions. Here, we report that, under anaerobic conditions, iron-sulfur proteins in E. coli cells are even more susceptible to copper in medium. Whereas addition of 0.2 mM copper(II) chloride to LB (Luria-Bertani) medium has very little or no effect on iron-sulfur proteins in wild-type E. coli cells under aerobic conditions, the same copper treatment largely inactivates iron-sulfur proteins by blocking iron-sulfur cluster biogenesis in the cells under anaerobic conditions. Importantly, proteins that do not have iron-sulfur clusters (e.g., fumarase C and cysteine desulfurase) in E. coli cells are not significantly affected by copper treatment under aerobic or anaerobic conditions, indicating that copper may specifically target iron-sulfur proteins in cells. Additional studies revealed that E. coli cells accumulate more intracellular copper under anaerobic conditions than under aerobic conditions and that the elevated copper content binds to the iron-sulfur cluster assembly proteins IscU and IscA, which effectively inhibits iron-sulfur cluster biogenesis. The results suggest that the copper-mediated inhibition of iron-sulfur proteins does not require oxygen and that iron-sulfur cluster biogenesis is the primary target of anaerobic copper toxicity in cells

Association of GSDMD with microvascular-ischemia reperfusion injury after ST-elevation myocardial infarction

ObjectivesLittle is known about the clinical prognosis of gasdermin D (GSDMD) in patients with ST-elevation myocardial infarction (STEMI). The purpose of this study was to investigate the association of GSDMD with microvascular injury, infarction size (IS), left ventricular ejection fraction (LVEF), and major adverse cardiac events (MACEs), in STEMI patients with primary percutaneous coronary intervention (pPCI).MethodsWe retrospectively analyzed 120 prospectively enrolled STEMI patients (median age 53 years, 80% men) treated with pPCI between 2020 and 2021 who underwent serum GSDMD assessment and cardiac magnetic resonance (CMR) within 48 h post-reperfusion; CMR was also performed at one year follow-up.ResultsMicrovascular obstruction was observed in 37 patients (31%). GSDMD concentrations ≧ median (13 ng/L) in patients were associated with a higher risk of microvascular obstruction and IMH (46% vs. 19%, P = 0.003; 31% vs. 13%, P = 0.02, respectively), as well as with a lower LVEF both in the acute phase after infarction (35% vs. 54%, P &lt; 0.001) and in the chronic phase (42% vs. 56%, P &lt; 0.001), larger IS in the acute (32% vs. 15%, P &lt; 0.001) and in the chronic phases (26% vs. 11%, P &lt; 0.001), and larger left ventricular volumes (119 ± 20 vs. 98 ± 14, P = 0.003) by CMR. Univariable and multivariable Cox regression analysis results showed that patients with GSDMD concentrations ≧ median (13 ng/L) had a higher incidence of MACE (P &lt; 0.05).ConclusionsHigh GSDMD concentrations in STEMI patients are associated with microvascular injury (including MVO and IMH), which is a powerful MACE predictor. Nevertheless, the therapeutic implications of this relation need further research