Kastrupschwarz6013

The present work aimed to evaluate the reactivity of natural bioflavonoid hesperidin (HSP) and synthetically derived XAV939 (XAV) against human hepatocellular carcinoma (HepG2), human breast cancer (MDA-MB231) cancer cell lines, and related molecular and pathological profiles. Data recorded revealed that the cytotoxic potential of the tested products was found to be cell type- and concentration-dependent. The half-maximal inhibitory concentration (IC50) value of the HSP-XAV mixture against MDA-MB231 was significantly decreased in the case of using the HSP-XAV mixture against the HepG2 cell line. Also, there was a significant upregulation of the phosphotumor suppressor protein gene (P53) and proapoptotic genes such as B-cell lymphoma-associated X-protein (Bax, CK, and Caspase-3), while antiapoptotic gene B-cell lymphoma (Bcl-2) was significantly downregulated compared with the untreated cell control. The cell cycle analysis demonstrated that DNA accumulation was detected mainly during the G2/M phase of the cell cycle accompanied with the elevated reactive oxygen species level in the treatment of HepG2 and MDA-MB231 cell lines by the HSP-XAV mixture, more significantly than that in the case of cell control. Finally, our finding suggests that both HSP and XAV939 and their mixture may offer an alternative in human liver and breast cancer therapy.Glycosyl phosphate repeating units can be found in the glycoconjugates of some bacteria and protozoa parasites. These structures and their P-modified analogs are attractive synthetic targets as antimicrobial, antiparasitic, and vaccine agents. However, P-modified glycosyl phosphates exist in different diastereomeric forms due to the chiral phosphorus atoms, whose configuration would highly affect their physiochemical and biochemical properties. In this study, a stereocontrolled method was developed for the synthesis of P-modified glycosyl phosphate repeating units derived from the lipophosphoglycan of Leishmania using the oxazaphospholidine approach. The solid-phase synthesis facilitated the elongation and purification of the glycosyl phosphate derivatives, while two P-modified glycosyl phosphates (boranophosphate and phosphorothioate) were successfully synthesized with up to three repeating units.Long-life and self-powered betavoltaic batteries are extremely attractive for many fields that require a long-term power supply, such as space exploration, polar exploration, and implantable medical technology. Organic lead halide perovskites are great potential candidate materials for betavoltaic batteries due to the large attenuation coefficient and the long carrier diffusion length, which guarantee the scale match between the penetration depth of β particles and the carrier diffusion length. However, the performance of perovskite betavoltaics is limited by the fabrication process of the thick and high-crystallinity perovskite film. In this work, we demonstrated high-performance perovskite betavoltaic cells using thick, high-quality, and wide-band-gap MAPbBr3 polycrystalline films. The solvent annealing method was adopted to improve the crystallinity and eliminate the pinholes in the MAPbBr3 film. The optimal MAPbBr3 betavoltaic cell achieved a power conversion efficiency (PCE) of 5.35% and a maximum output power of 1.203 μW under radiation of electrons of 15 keV with an equivalent activity of 253 mCi. These results are a nearly 50% improvement from previous reports. Effects of the MAPbBr3 perovskite layer thickness on the device performance were also discussed. The mechanisms of film-growth processes and device physics could provide insights for the research community of perovskites and betavoltaics.Waste palm kernel cake (WPKC) is being utilized as a biomass feedstock for the sustainable production of catalysts/supports and bio-oil fuels. Herein, metal (Cu, Ni, and/or Fe)-doped carbon catalysts were prepared using conventional impregnation and pyrolysis methods. The physicochemical properties of the as-prepared catalysts were analyzed. According to the obtained results, the catalyst acidity was highly increased with the increase in the metal loading amount on a carbon support, leading to a better performance for deoxygenation/aromatization. A maximum yield of bio-oil from WPKC pyrolysis was achieved up to ∼60% under optimum conditions determined via statistical designs. From the results of bio-oil compositions, 15%Ni loading on activated carbon exhibited the best performance of about 72% for the production of hydrocarbon compounds. Monoaromatic hydrocarbons such as benzene, toluene, and xylenes (BTXs) could be reduced via condensation and polymerization with the increase of the Ni-loading amount. learn more Moreover, the catalytic performance of the selected 15%Ni-carbon catalyst was also compared with those of commercial catalysts zeolite and alumina, and the results showed that the 15% metal-doped carbon catalyst presented much better stability/reusability for five times with less reduction of the hydrocarbon yield in the upgraded bio-oil. This research provided an eco-friendly strategy for the low-cost production of bio-oil fuel with a high quality/yield from waste biomass pyrolysis.The results of experimental investigations on the coking of decanted heavy gasoil of catalytic cracking with polystyrene in a certain concentration range to obtain petroleum needle coke with the most developed string-base anisotropic structure and a microstructure point of at least 6.2 corresponding to the super-premium grade are presented. Certain regularities have been established to improve the structural quality index of the resulting needle coke from the optimal content of polystyrene in the base raw material, including the extreme dependence of the quality indices of needle coke on the polystyrene content (10 wt %). The decrease in the quality indices of the obtained carbon material is a consequence of uncontrolled changes toward an increase in the system viscosity performance (the viscosity increases 2.7 times). link2 The experimentally obtained coefficient of thermal expansion (CTE) of needle coke-synthesized samples within the temperature range of 40-500 °C showed a reducing trend in CTE depending on the polymer additive proportion in the feedstock; for example, at 300 °C, the CTE decreases to 5.732 × 10-6 °C-1.MXenes, a family of two-dimensional transition-metal carbides/nitrides, have attracted great attention and shown promising application in polymer composites. In this study, a typical MXene Ti3C2T x was prepared by selective etching. The structure and morphology of Ti3C2T x were studied by X-ray diffraction (XRD), scanning electron microscopy, and transmission electron microscopy, and the results proved that Ti3C2T x was successively fabricated. Then, Ti3C2T x /isotactic polypropylene composites with different Ti3C2T x dosages were fabricated, and the nonisothermal crystallization kinetics and melting behavior of the composites were investigated. The results indicated that when a small amount of Ti3C2T x was added, the crystallization parameters including the crystallization peak temperature and the crystallization rate increased, suggesting that crystallization was promoted. When the weight percentage of Ti3C2T x exceeded 1%, the crystallization parameters showed a reverse trend, suggesting that crystallization was hindered. The activation energy of composites with 0, 0.25, 0.5, and 1 wt % Ti3C2T x were calculated to be -164.5, -196.5, -193.8, and -147.95 kJ/mol, respectively, revealing that the crystallization of composites is concentration-dependent. The impact of Ti3C2T x dosage on the crystalline structure of the composites was studied using XRD. The related mechanism was proposed.The mixing Gibbs free energy and formation enthalpy difference of different Ti-doped (Nb1-x Ti x )C complex carbides were calculated using the Cambridge Serials Total Energy Package (CASTEP) module of Materials Studio 2019 software. The calculation results predict that (Nb1-x Ti x )C complex carbides have higher stability than pure NbC and TiC. Therefore, three lightly Ti-doped (Nb1-x Ti x )C complex carbides with theoretical densities close to that of the 1045 steel were designed for calculations. The calculation results show that the formation energy of (Nb1-x Ti x )C complex carbides decreases with an increase in the Ti content. These designed (Nb1-x Ti x )C complex carbides have mechanical stability, and their bulk modulus, shear modulus, Young's modulus, and hardness are all lower than those of pure NbC. The electronic performance results show that these three structures show good conductivity, and the 3d orbitals of Ti atoms and the 4d orbitals of Nb atoms are strongly hybridized with the 2p orbitals of C atoms. The Nb-C and Ti-C bonds exhibit strong covalent bonds. link3 To verify the stability of the (Nb1-x Ti x )C complex carbides, the prepared (Nb0.8Ti0.2)C complex carbide was added to the 1045 steel as a refiner. After observing under a transmission electron microscope (TEM), we found that the (Nb0.8Ti0.2)C complex carbide could exist stably as a face-centered cubic structure, which provided a method for the design and synthesis of complex carbides used for refiners.In this study, we describe a practical and facile synthesis of deuterium-labeled indoles via acid-catalyzed hydrogen-deuterium exchange. 3-Substituted indoles were efficiently deuterated through treatment with 20 wt % D2SO4 in CD3OD at 60-90 °C. A deuterium incorporation reaction of 3-unsubstituted indoles was accomplished through treatment with CD3CO2D at 150 °C. The in situ preparation of a 20 wt % D2SO4/CH3OD/D2O solution enabled a large-scale and low-cost synthesis of auxins, indole-3-acetic acid-d5 and indole-3-butyric acid-d5.For a thorough mechanistic understanding of reverse osmosis (RO), data on ion retention obtained by desalination of multi-ionic solutions are needed. In this paper, we show how to obtain such data under controlled laboratory conditions at any nonextreme pH. For that, we propose a simple method where we use N2 and CO2 gas control to set the composition of a gas phase in equilibrium with the feedwater solution. By increasing the CO2 partial pressure, the pH of the solution will decrease and vice versa. We applied this method of CO2 gas control to extend and validate an existing data set on ion retention of multi-ionic brackish water with 10 different ionic species, whereas conditions in the prior data set were slightly uncontrolled; in our new analysis, we performed experiments at precisely controlled pH and temperature. We run experiments at pH 6.73 and pH 7.11 and in a temperature range of T = 15-31 °C. Our results show that when pH is decreased, or temperature increased, the ion retention of most ions decreases. We also tested the influence of the Na+ to Ca2+ concentration ratio in this multi-ionic solution on ion retention at pH 6.73 and T ∼ 31 °C. We noticed that this ratio has a larger effect on ion retention for cations than for anions. We compare our data with the earlier reported data and describe similarities and differences. The improved data set will be an important tool for future development of accurate and validated RO ion transport models. Such RO models that describe desalination performance in detail are important for successful commercial application of the RO technology. We also discuss a relevant preparation method for water slightly oversaturated with barely soluble CaCO3 by solution preparation at high CO2 pressure, after which the solution is brought to the required pH by the N2 and CO2 gas control method.