Changes in proton currents in murine microglia induced by cytoskeletal disruptive agents

The sera of 385 buffaloes of different age and sex, collected from the various areas of the Khoozestan province, Iran, were tested by the IFA test, from April 1995 to February 1996. The results indicated 8.8% (34 out of 385) buffaloes had anti-Toxoplasma gondii antibodies titered 1:16 and more. The infection rate of buffaloes under the age of a year, above a year female, and male were 10.8%, 4.7%, 12.1%, and 5.3%, respectively.     

The 3D model: explaining densification and deformation mechanisms by using 3D parameter plots

The aim of the study was to analyze very differently deforming materials using 3D parameter plots and consequently to gain deeper insights into the densification and deformation process described with the 3D model in order to define an ideal tableting excipient. The excipients used were dicalcium phosphate dihydrate (DCPD), sodium chloride (NaCl), microcrystalline cellulose (MCC), xylitol, mannitol, alpha-lactose monohydrate, maltose, hydroxypropyl methylcellulose (HPMC), sodium carboxymethylcellulose (NaCMC), cellulose acetate (CAC), maize starch, potato starch, pregelatinized starch, and maltodextrine. All of the materials were tableted to graded maximum relative densities (rhorel, max) using an eccentric tableting machine. The data which resulted, namely force, displacement, and time, were analyzed by the application of 3D modeling. Different particle size fractions of DCPD, CAC, and MCC were analyzed in addition. Brittle deforming materials such as DCPD exhibited a completely different 3D parameter plot, with low time plasticity, d, and low pressure plasticity, e, and a strong decrease in omega values when densification increased, in contrast to the plastically deforming MCC, which had much higher d, e, and omega values. e and omega values changed only slightly when densification increased for MCC. NaCl showed less of a decrease in omega values than DCPD did, and the d and e values were between those of MCC and DCPD. The sugar alcohols, xylitol and mannitol, behaved in a similar fashion to sodium chloride. This is also valid for the crystalline sugars, alpha-lactose monohydrate, and maltose. However, the sugars are more brittle than the sugar alcohols. The cellulose derivatives, HPMC, NaCMC, and CAC, are as plastic as MCC, however, their elasticity depends on substitution indicated by lower (more elastic) or higher (less elastic) omega values. The native starches, maize starch and potato starch, are very elastic, and pregelatinized starch and maltodextrine are less elastic and exhibited higher omega values. Deformation behavior as shown in 3D parameter plots depends on particle size for polymers such as CAC and MCC; however, it does not depend on particle size for brittle materials such as DCPD. An ideally deforming tableting excipient should exhibit high e, d, and omega values with a constant ratio of e and omega at increasing densification.     

Vortex-induced flame extinction in two-phase counterflow diffusion flames with CH planar laser-induced fluorescence and particle-image velocimetry

Here the interaction between a laminar two-phase, non-pre-mixed counterflow flame and a vortex is examined. Special emphasis is given to the influence of different flame and vortex parameters on the extinction behavior of the flame. Simultaneous planar laser-induced fluorescence of the CH radical layer produced by the flame and particle-image velocimetry measurements of the flowfield are used to characterize the flame-vortex interaction. These simultaneous diagnostics are used for the first time in this configuration. The extinction processes occurring during the flame-vortex interaction can be analyzed by this method, especially the influence of strain at the flame surface. The influence of the droplets on the extinction behavior appears clearly compared with a fully gaseous flame. The spray flame is weaker and extinguishes earlier than does a gaseous flame. In the measurements an additional broadband signal in the vicinity of the CH layer is probably due to the induced fluorescence of polycyclic aromatic hydrocarbons, excited at the same wavelength.     

Thermal Conductivity of Aqueous Sugar Solutions under High Pressure

Molecular energy transport in aqueous sucrose and glucose solutions of different mass fractions and temperatures is investigated up to 400 MPa, using the transient hot-wire method. The results reveal an increasing thermal conductivity with increasing pressure and decreasing mass fraction of sugar. No significant differences between sucrose and glucose solutions were observed. Different empirical and semi-empirical relations from the literature are discussed to describe and elucidate the behavior of the solutions with pressure. The pressure-induced change of the thermal conductivity of sugar solutions is mainly caused by an increase of the thermal conductivity and the decrease of molar volume of the water fraction. A simple pressure adapted mass fraction model permits an estimation of the thermal conductivity of the investigated solutions within an uncertainty of about 3%. An erratum to this article can be found at     

P450 BM3 Monooxygenase as an Efficient NAD(P)H‐Oxidase for Regeneration of Nicotinamide Cofactors in ADH‐Catalysed Preparative Scale Biotransformations

Enzymatic oxidations of primary and secondary alcohols catalysed by nicotinamide dependent alcohol dehydrogenases on the preparative scale require cofactor regeneration systems. Of critical value from an economic and ecological perspective is the application of NAD(P)H‐oxidases, which utilise molecular oxygen as a cost‐effective, atom‐efficient and environmentally benign oxidant to regenerate the cofactor NAD(P)⁺. Herein, the P450 BM3 monooxygenase from Bacillus megaterium is presented as an NAD(P)H‐oxidase for the successful regeneration of both NADP⁺ and NAD⁺ on the preparative scale. This enzyme was exemplarily applied for ADH‐catalysed oxidative kinetic resolutions of racemic secondary alcohols and the desymmetrisation of a meso‐diol leading to enantiomerically enriched secondary alcohols in both cases. Furthermore, the ADH‐catalysed oxidation of a primary alcohol targeting the corresponding aldehyde was performed. The obtained results significantly broaden the scope of feasible oxidative biotransformations, thereby increasing the number of synthetic reactions complying with key challenges of a modern and sustainable chemistry such as mild reaction conditions, environmentally benign solvents, and biodegradable non‐toxic catalysts.

     

Advanced chemically induced phase separation in thermosets: Polybenzoxazines toughened with multifunctional thermoplastic main-chain benzoxazine prepolymers

Multifunctional thermoplastic main-chain benzoxazine prepolymers were synthesized and systematically varied in their structure in order to function as high-performance toughener additives. Their unique chemical composition allows multiple covalent crosslinking with many thermoset network systems including benzoxazines and epoxides in conjunction with a defined chemical induced phase separation (CIPS) upon curing. This was successfully shown using a benzoxazine-based thermoset resin matrix as an example. The corresponding morphologies were addressable in a predictable manner and brought into context with the obtained macroscopic mechanical and thermal properties. In this relationship the CIPS process was classified and compared with the literature in more general means for advanced morphology control by differentiating between covalently attached and so-called gradient domain structures. The prepolymers were characterized by ¹H NMR, FT-IR, DSC and TGA. The thermoset morphologies were investigated by TEM and AFM. The fracture toughness (K_Ic) and the elastic modulus (E) were measured by fracture and three point bending experiments. Thermal properties of the resulting films have been tested by DMA.