Mineralocorticoid hormone receptor and the epithelial sodium channel in a human leukemic cell line

A Cell extract from the HEL (human erythroblastic leukemia) cell line was positive for both the epithelial sodium channel (ENaC) and the mineralocorticoid receptor (MCR) as glycosylated 82-84 kDa bands, and a single 102 kDa band, respectively, in Western blots using polyclonal antibodies raised against these proteins. The immunofluorescent labeling of the MCR in all cell lines showed a nucleocytoplasmic localization of the receptor whereas the ENaC was exclusively membrane-bound. These results were confirmed by confocal microscopy. The expression of the MCR in HEL cells was evident as a predicted band of 843 bp (234 amino acids) after total RNA from HEL cells had been reverse transcribed and then amplified by PCR; the ENaC was similarly evident as a predicted band of 520 bp. In both cases, near 100% identity was observed between the deduced amino acid sequences of the PCR products and those from known human sources. The multiplication of HEL cells was influenced by antagonists (RU 26752, ZK 91587) targeted for specificity to the MCR and this was reversed by the natural hormone aldosterone. These steroids also provoked chromatin condensation in the HEL population.     

Refractory concretes uniaxial compression behaviour under high temperature testing conditions

Two refractory concretes with the same matrix composition, one based on andalusite aggregate and the other on bauxite aggregate, have been studied at temperatures ranging from room temperature to 1200 °C maximal temperature. Samples dried at 110 °C during 24 h to create dried standard specimens and others, fired at different temperatures, were subjected to several uniaxial compression test conditions conducted at various temperatures. The evolution of the materials’ global behaviour from quasi-brittle to viscous was evidenced and correlated to their microstructure evolution. Loading/unloading, creep, and strain rate jump tests helped define the damageable and viscoplastic nature of the behaviour. The influence of the firing temperature and duration on the materials’ behaviour is also reported and discussed. In conclusion, potential constitutive equations that are able to fit the material recorded behaviour are suggested.     

Crystal chemistry of the monazite structure

The AXO₄ monazite-type compounds form an extended family that is described in this review in terms of field of stability versus composition. All the substitution possibilities on the cationic and anionic sites leading to the monazite structure are reported. The phosphate, vanadate, chromate, arseniate, sulphate and silicate families are described and the unit-cell parameters of pure compounds and solid solutions are gathered. The stability limits of the monazite-type structure are discussed versus several models generally correlated with geometric criteria. The effects of physico-chemical parameters such as pressure, temperature and irradiation on the monazite-type structure stability are also discussed. The structural relationships between the monazite structure and the related structures (zircon, anhydrite, barite, AgMnO₄, scheelite and monoclinic BiPO₄, CaSeO₃, rhabdophane and SrNp(PO₄)₂) are described.     

Silver coated aluminium microrods as highly colloidal stable SERS platforms

We report on the fabrication of a novel material with the ability to remain in solution even under the very demanding conditions required for structural and dynamic characterization of biomacromolecule assays. This stability is provided by the increase in surface area of a low density material (aluminium) natively coated with a very hydrophilic surface composed of aluminium oxide (Al(2)O(3)) and metallic silver nanoparticles. Additionally, due to the dense collection of active hot spots on their surface, this material offers higher levels of SERS intensity as compared with the same free and aggregated silver nanoparticles.     

Optimization of post-combustion CO2 process using DEA-MDEA mixtures

This paper presents optimal operating conditions for the post-combustion CO₂ capture process utilizing aqueous amine solutions obtained using a process simulator (HYSYS). Three alkanolamine solutions (Methyldiethanolamine MDEA, DiEthanolAmine DEA and MDEA-DEA mixture) are considered to study the performance of the capture process.The design problem addressed in this paper requires specifying the optimal operating conditions (inlet and outlet temperature of the lean solution stream on the absorber, CO₂ loading, amine composition and flow rates, among others) to achieve the given CO₂ emission targets at a minimum total annual cost. A detailed objective function including total operating costs and investment is considered.The influence of the variation of CO₂ reduction targets and the mixing proportion of amines on the total annual cost is analyzed in detail. Numerical results are presented and discussed using different case studies.The results demonstrate that process simulators can be used as a powerful tool not only to simulate but also to optimize the most important design parameters of the post-combustion CO₂ capture process.     

Inulin mixed esters crosslinked with 2-ethyl-hexyl-acrylate and their promotion as bio-based materials

New inulin-based materials were obtained by graft-copolymerization of inulin (poly-β(1 → 2)-fructoside) with 2-ethyl-hexyl acrylate. Inulin mixed esters were first synthesized by acylation using methacryloyl and palmitoyl chlorides. Further, these esters were copolymerized with 2-ethyl-hexyl acrylate in order to obtain bio-based crosslinked materials that could be used as commodity plastics and that would have biodegradable properties. The obtained products were characterized using FT-IR and ¹H NMR spectroscopies, thermogravimetry; differential scanning calorimetry, and activation energy for the degradation processes (using Kissinger method) was calculated. These biomaterials were also subjected to density measurement, tensile and torsion tests to evaluate their mechanical properties.     

Dislocation Cores and Hardness Polarity of 4H-SiC

The hardness of opposite basal faces of 4H-SiC single crystals has been measured in the temperature range 25°–1200°C. A strong hardness anisotropy between the silicon-terminated (0001) and carbon-terminated (0001) faces of this polar crystal has been found. Transmission electron microscopy investigation of the dislocations in the plastic zone of the 1200°C indentations shows that they lie predominantly on the basal planes parallel to the indented face, and the extra-half planes of the nonscrew dislocations originate from the indented face. It is also found that, when the (0001) Si-terminated face is indented, the dislocations are either widely dissociated, with the width of the stacking fault ribbon much larger than the equilibrium value, or else they are single leading partials, with the corresponding trailing partials absent. In this case, all the leading partials are found to have a silicon core. On the other hand, the dislocations in the plastic zone of the carbon-terminated face are in the form of dissociated dislocations, with the width of the associated stacking fault ribbons appreciably less than the equilibrium value. Moreover, the leading partials of these dissociated dislocations have a carbon core. The results indicate that the hardness of the polar basal faces of 4H-SiC at elevated temperatures is partly determined by the nature of the dislocation cores nucleated by the indentation process. It is argued that this is due to the influence of the core on the generation and glide of the leading partial dislocations.     

Transport properties of natural gas through polyethylene nanocomposites at high temperature and pressure

Four titanium(IV) alkoxides, namely: Ti(IV) n-propoxide (1), Ti(IV) n-butoxide (2), Ti(IV) tert-butoxide (3), and Ti(IV) 2-ethylhexoxide (4), have been used as initiators in the bulk ring-opening polymerization (ROP) of ??-caprolactone (??-CL). The influence of the alkoxide group on the course of the ROP of ??-CL was investigated by means of ¹H-NMR and differential scanning calorimetry (DSC). The ¹H-NMR spectra confirmed that the ROP reaction of ??-CL proceeded via the widely accepted coordination-insertion mechanism for each of the four initiators. Isoconversional methods have been used to evaluate non-isothermal DSC data via the equations of Friedman, Kissinger-Akahira-Sunose (KAS) and Ozawa-Flynn-Wall (OFW). The kinetic studies showed that the polymerization rate for the four initiators (1-4) was in the order of 1?>?2????4?>?3. The lowest activation energies (40?C47, 42?C44, and 49?C52?kJ/mol for the Friedman, KAS and OFW methods respectively) were found in the polymerizations using Ti(IV) n-propoxide (1), while the highest activation energies (84?C107, 77?C87, and 80?C91?kJ/mol for the Friedman, KAS and OFW methods respectively) were obtained using Ti(IV) tert-butoxide (3). Differences in the rates of polymerization and the activation energies amongst the four initiators appeared to be governed mainly by the different degrees of steric hindrance in the initiator structure. These results represent important findings regarding the steric influence of the alkoxide groups on the kinetics of the ROP of ??-CL initiated by titanium(IV) alkoxides.     

Effect of Oxime Ether Incorporation in Acyl Indole Derivatives on PPAR Subtype Selectivity

Compounds that simultaneously activate peroxisome proliferator‐activated receptor (PPAR) subtypes α and γ have the potential to effectively treat dyslipidemia and type 2 diabetes (T2D) in a single pharmaceutically active molecule. The frequently observed side effects of selective PPARγ agonists, such as edema and weight gain, were expected to be overcome by using additive PPARα activity, leading to dual PPARα/γ agonists with balanced activity for both subtypes. Herein we report the discovery, synthesis, and optimization of a new series of α‐ethoxyphenylpropionic acid bearing 5‐ or 6‐substituted indoles. The incorporation of oxime ethers on the carbonyl portion of the benzoyl group can bring the PPARα/γ potency ratio equal to or slightly greater than one, as is the case for compounds 20 c and 21 a . Compound 20 c shows high efficacy in an ob/ob mouse model of T2D and dyslipidemia, similar to that of rosiglitazone and tesaglitazar, but with a significant increase in body weight gain. In contrast, compound 21 a , less potent as a dual PPARα/γ activator than 20 c , showed an interesting pharmacological profile, as it elicits a decrease in body weight relative to reference compounds.     

Thiol-ene “clickable” carbon-chain polymers based on diallyl cyclopropane-1,1-dicarboxylate

A novel type of clickable polymers with a very high local density of allyl side groups was developed. These polymers were obtained by the anionic ring-opening (co)polymerization of diallyl cyclopropane-1,1-dicarboxylate using as an initiating system a protic precursor whose acid–base reaction with the t-BuP₄ phosphazene base generated the initiator in situ. The obtained polymers display geminated allyl groups on every third carbon alongside the macromolecular backbone. Homopolymers as well as block and statistical copolymers have been synthesized, with controlled molecular weights and narrow molecular weight distributions. The coupling of mercaptans with the allyl CC double bonds has been investigated both thermally and photochemically, with the influence of the type of initiation on the efficiency of the polymer modification being discussed in comparison with other “clickable” systems. Further functionalization by several thiols was performed, leading to a range of functional poly(cyclopropane-1,1-dicarboxylate)s.