Effects of fibinolysis on neurite growth from dorsal root ganglia cultured in two- and three-dimensional fibrin gels

The mechanism of neurite penetration of three-dimensional fibrin matrices was investigated by culturing embryonic chick dorsal root ganglia (DRGs) within fibrin gels, upon fibrin gels, and upon laminin. The length of neurites within three-dimensional matrices of fibrin was decreased in a concentration-dependent manner by agents that inhibited plasmin, e.g. aprotinin, or that inhibited plasminogen activation, e.g., epsilon-aminocaproic acid (EACA), or plasminogen antiserum. In contrast, such agents increased the length of neurites growing out from DRGs cultured upon two-dimensional substrates of fibrin and had no effect on the length of neurites growing out from DRGs cultured upon laminin. Visualization of neurites within three-dimensional fibrin matrices demonstrated that the distance between fibrin strands was much smaller than the diameter of neurites. All these data were consistent with the hypothesis that fibrinolysis localized to the region of the neurite tip is an important mechanism for neurite penetration of a physical barrier of fibrin strands arranged in a three-dimensional matrix.     

Sydnon-äthylene. I Stereoselektive Darstellung von Sydnon-äthylenen aus Sydnon-aldehyden

Sydnone Ethylenes. I Stereoselective Synthesis of Sydnone Ethylenes from Sydnone Aldehydes Sydnones are formylated in 4-position by the VILSMEIER -HAAK reaction. N(3)-Methyl- and N(3)-(p-Anisyl)-sydnone-(4)-carboxaldehyde react stereoselectively to sydnone ethylenes with diethyl ethoxycarbonylmethanephosphonate by HORNER reaction and with arylmethylphosphonium salts by WITTIG reaction in the presence of strong bases. In the latter case, especially in the absence of lithium cations, Z-selectivity is observed which is explained by electronic interaction between the sydnone cyclus and the aromatic substituent of the phosphine ylid in the first step of the reaction. The configuration of the obtained Z- and E-sydnone ethylenes is determined by means of ¹H-NMR- and IR-spectra.     

Permittivity of modified polyimide layers on LTCC

In this work, the permittivity of a tailored compound material was investigated consisting of a polyimide matrix in which hollow glass microspheres with a mean diameter of 30 μm are implemented as filler material. Choosing this approach the dielectric constant compared to that of the pure polyimide material is further decreased due to the enclosed air targeted to improve the high-frequency performance of patch antennas operated in the GHz range. Furthermore, the thickness of one single layer can be increased substantially from a maximum of about 10 μm for pure polyimide films to values above 80 μm by simply adding this type of filler material to the liquid polyimide precursor so that cavities in LTCC (low temperature co-fired ceramics) substrates can be filled more reliable. Two different variations of this compound material with filler to polymer ratios of 1:7.5 and 1:10 are realized. Basically, the film thickness depends on the spin coating speed and the microsphere content, respectively. The high initial surface roughness can be decreased to an average value of about 3 μm by applying additional layers of pure polyimide on top enabling thin film technology. The dielectric constant of the complete substrate comprising the LTCC and the compound material is measured using a ring resonator in microstrip configuration. From the resonances occurring in the transmission S-parameter |S₂₁| spectrum between 1 and 10 GHz, the relative dielectric constant can be determined. Using 820 μm thick LTCC substrates the permittivity can be reduced from originally ε_r = 7.8-6.6. By applying numerical calculations, a reduced permittivity of the pure polymer film from ε_r = 3.3 to about 2.9 can be determined when adding the glass microspheres.     

Formulation for chemical EOR: Development and evaluation of an ASP formulation In customer field conditions

Alkali surfactant polymer (ASP) flooding is an enhanced oil recovery (EOR) technology with an impressive potential for increasing incremental oil production from conventional hydrocarbon bearing reservoirs. A challenge to ASP application is the complexity of determining an effective formulation, typically requiring extensive laboratory screening of nearly countless combinations of surfactants and cosolvents. This paper focuses on demonstrating the utility of the hydrophilic–lipophilic deviation (HLD) concept for EOR application to simplify surfactant formulation workstreams seeking an economically viable ASP formulation for field application. In describing work performed for EOR application of ASP under customer conditions using crude oil, the discussion covers the initial evaluation of the promising surfactant formulation (interfacial tension and solubility), the improvement upon the formulation via HLD principles, and the evaluation of the improved surfactant formulation (coreflood studies). The final ASP formulation identified consisted of a 9 to 1 mixture of alkyl propoxy sulfate sodium salt (APS) to alkyl ethoxy sulfate sodium salt (AES) totaling 2000 ppm active surfactant content, 2.0 wt% Na₂CO₃, and 3000 ppm polyacrylamide polymer (all commercially available products). This formulation had ultra-low interfacial tension and favorable mixing behavior under reservoir conditions. In coreflood studies, the final formulation reproducibly achieved cumulative oil recovery of 96.4%–98.5% of original oil in place with only 0.3 PV of ASP injection with a chase alkali polymer injection.     

Mathematical Description of Experimentally Determined Charge Distributions of a Unipolar Diffusion Charger

The charge distributions of an improved opposed flow unipolar diffusion charger were measured using a tandem differential mobility analyzer (DMA) set up in a size range of approximately 20–400 nm. The charger is intended to be used in a portable aerosol sizer to measure particle size distributions. The determined charge distributions were represented by lognormal distributions, and a set of equations and coefficients was developed to calculate the charge distributions. These equations can be easily implemented in software for size distribution measurements. The agreement between the mathematically derived and measured charge distributions is very good, with regression coefficients R ² > 0.96. The investigations showed that approximately 55% of 20-nm particles remain uncharged, while up to 25 elementary charges need to be considered for multiple charge correction of 400-nm particles. Comparison with the Fuchs theory delivered satisfying agreement with the measured average charge levels, but charge distributions cannot be described by the Fuchs theory, likely caused by the charger geometry.

Copyright 2012 American Association for Aerosol Research     

Modeling Alcohol Dehydrogenase Catalysis in Deep Eutectic Solvent/Water Mixtures

The use of oxidoreductases (EC1) in non-conventional reaction media has been increasingly explored. In particular, deep eutectic solvents (DESs) have emerged as a novel class of solvents. Herein, an in-depth study of bioreduction with an alcohol dehydrogenase (ADH) in the DES glyceline is presented. The activity and stability of ADH in mixtures of glyceline/water with varying water contents were measured. Furthermore, the thermodynamic water activity and viscosity of mixtures of glyceline/water have been determined. For a better understanding of the observations, molecular dynamics simulations were performed to quantify the molecular flexibility, hydration layer, and intraprotein hydrogen bonds of ADH. The behavior of the enzyme in DESs follows the classic dependence of water activity (a_W) in non-conventional media. At low a_W values (<0.2), ADH does not show any activity; at higher a_W values, the activity was still lower than that in pure water due to the high viscosities of the DES. These findings could be further explained by increased enzyme flexibility with increasing water content.     

Triethylsulfonium Bistriflimide as the Reaction Medium in Catalyzed and Uncatalyzed Cycloaddition [4 + 2]

Triethylsulfonium bistriflimide, [S_2.2.2][NTf₂], has been tested and compared with other ionic liquids and molecular solvents as a medium in Diels–Alder reaction between cyclopentadiene and dimethyl maleate. Triflates and chlorides of different metals have been combined with [S_2.2.2][NTf₂] and the catalytic activity of the systems formed have been determined. The effect of concentration of the catalysts in sulfonium ionic liquid and reactants on the yield and endo:exo ratio has been established. The representative catalyst—Yb(OTf)₃·xH₂O in [S_2.2.2][NTf₂] has been examined in the reaction of cyclopentadiene with various dienophiles. The use of sulfonium ionic liquids permitted recycling the catalysts. For the best four catalytic systems, the products have been isolated.