Fluorescence probing of the temperature-induced phase transition in a glycolipid self-assembly: hexagonal ↔ micellar and cubic ↔ lamellar

Water-driven self-assembly of lipids displays a variety of liquid crystalline phases that are crucial for membrane functions. Herein, we characterize the temperature-induced phase transitions in two compositions of an aqueous self-assembly system of the octyl β-D-glucoside (βGlcOC(8)) system, using steady-state and time-resolved fluorescence measurements. The phase transitions hexagonal ? micellar and cubic ? lamellar were investigated using tryptophan (Trp) and two of its ester derivatives (Trp-C(4) and Trp-C(8)) to probe the polar headgroup region and pyrene to probe the hydrophobic tail region. The polarity of the headgroup region was estimated to be close to that of simple alcohols (methanol and ethanol) for all phases. The pyrene fluorescence indicates that the pyrene molecules are dispersed among the tails of the hydrophobic region, yet remain in close proximity to the polar head groups. Comparing the present results with our previously reported one for βMaltoOC(12), increasing the tail length of the hexagonal phase from C(8) to C(12) leads to less interaction with pyrene, which is attributed to the more random and wobbling motion of the longer alkyl tail. We measured a reduction (more hydrophobic) in the ratio of the vibronic peak intensities of pyrene (I(1)/I(3)) for the lamellar phase compared to that of the cubic phase. The higher polarity in the cubic phase can be correlated to the nature of its interface, which curves toward the bulk water. This geometry also explains the slight reduction in polarity of the headgroup region compared to the other phases. Upon the addition of Trp-C(8), the fluorescence lifetime of pyrene is reduced by 28% in the lamellar and cubic phases, whereas the I(1)/I(3) value is only slightly reduced. The results reflect the dominant role of dynamic interaction mechanism between the C(8) chain of Trp-C(8) and pyrene. This mechanism may be important for these two phases since they participate in the process of membrane fusion. Both lipid compositions show completely reversible temperature-induced phase transitions, reflecting the thermodynamic equilibrium structures of their mesophases. Probing both regions of the different lipid phases reveals a large degree of heterogeneity and flexibility of the lipid self-assembly. These properties are crucial for carrying out different biological functions such as the ability to accommodate various molecular sizes.     

Antioxidant, antimicrobial and tyrosinase inhibitory activities of xanthones isolated from Artocarpus obtusus F.M. Jarrett

One of the most promising plants in biological screening test results of thirteen Artocarpus species was Artocarpus obtusus FM Jarrett and detailed phytochemical investigation of powdered dried bark of the plant has led to the isolation and identification of three xanthones; pyranocycloartobiloxanthone A (1), dihydroartoindonesianin C (2) and pyranocycloartobiloxanthone B (3). These compounds were screened for antioxidant, antimicrobial and tyrosinase inhibitory activities. Pyranocycloartobiloxanthone A (1) exhibited a strong free radical scavenger towards DPPH free radicals with IC50 value of 2 μg/mL with prominent discoloration observed in comparison with standard ascorbic acid, α-tocopherol and quercetin, The compound also exhibited antibacterial activity against methicillin resistant Staphylococcus aureus (ATCC3359) and Bacillus subtilis (clinically isolated) with inhibition zone of 20 and 12 mm, respectively. However the other two xanthones were found to be inactive. For the tyrosinase inhibitory activity, again compound (1) displayed strong activity comparable with the standard kojic acid.     

Identification and Separation of Lead (II), Nickel (II), and Cobalt (II) on Silica Gel 60 F254 High-Performance Thin-Layer Chromatographic Plates with Mixed Aqueous Sodium Dodecyl Sulfate—Oxalic Acid Solvent System

JPC – Journal of Planar Chromatography – Modern TLC - The chromatographic separation of three metal cations was performed on high-performance thin-layer plates (silica gel 60F254) with...     

Solving the generalized Burgers–Huxley equation using the Adomian decomposition method

In this paper, a convergence proof of the Adomian decomposition method (ADM) applied to the generalized nonlinear Burgers–Huxley equation is presented. The decomposition scheme obtained from the ADM yields an analytical solution in the form of a rapidly convergent series. The direct symbolic–numeric scheme is shown to be efficient and accurate.     

Computer simulation studies of anisotropic systems XIV. Binary mixtures of liquid crystals

We have simulated the behaviour of a model, binary mixture of nematogens composed of cylindrically symmetric particles using the Monte Carlo technique. The characteristics of the model mixture were chosen to be in accord with most of the assumptions made in the Humphries-James-Luckhurst theory of liquid crystalline mixtures. The results of the simulation experiments allow us to test, for the first time, the validity of the molecular field approximation in this theory. In addition to the second rank long range orientational order parameters for both components of the mixture we have also determined certain orientational pair correlation functions. These enable us to investigate the ability of one component to enhance the order of the other component or the same component in its vicinity.     

Electron conduction associated with the chemical transport of reducing elements in oxide cathode for CRT's application

In the present work, the formation of compounds associated to the diffusion of reducing elements (Mg, Al and W) to the Ni cap surface of oxide cathode has been studied by a new method. This method used two cathodes, one of them is coated and the other is uncoated, to be in an attach-contact mounted in a dummy tube. Different analytical techniques were used for this study: scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectroscopy (EDX) and I/V electrical measurements. After oxide cathode plus decomposited and activated, Al and Mg doping elements take place during heating to 810 °C (Ni-Br) under a rich controlled Ba/SrO atmosphere through an acceleration life test.It is shown that the chemical transport occurs mainly by a grain boundary mechanism with significant pile-up of Mg compounds. Al and W show a superficial concentrations and distribution.The dc electrical characteristic shows very strong rectifying behaviour through the M-S junction due to the I/V curves, particularly after 144 h acceleration life time. The characteristics are found to be reversible and reproducible, and viewed a rectification ratio (r) of 100. The calculated ideality factor shows a value of n = 9.6, which is evidenced to the tunnelling conduction.The theoretical calculation shows that the interface thickness grows to (∼6 μm) after accelerated the cathode to 1896 h.     

Markoff–Rosenberger triples and generalized Lucas sequences

Periodica Mathematica Hungarica - We consider the Markoff–Rosenberger equation $$\begin{aligned} ax^2+by^2+cz^2=dxyz \end{aligned}$$ with $$(x,y,z)=(U_i,U_j,U_k)$$ , where $$U_i$$ denotes the...     

Heterogeneous uptake and reactivity of formic acid on calcium carbonate particles: a Knudsen cell reactor, FTIR and SEM study

The heterogeneous uptake and reactivity of formic acid (HCOOH), a common gas-phase organic acid found in the environment, on calcium carbonate (CaCO(3)) particles have been investigated using a Knudsen cell reactor, Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM). FTIR measurements show that the adsorption of formic acid on the surface of calcium carbonate results in the formation of calcium formate. Besides calcium formate, carbonic acid is also a reaction product under dry conditions (<1% RH). Under dry conditions and at low pressures, the initial uptake coefficient of formic acid on CaCO(3) particles is measured to be 3 +/- 1 x 10(-3) and decreases as the surface saturates with adsorbed products. The maximum surface coverage of formic acid under dry conditions is determined to be (3 +/- 1)x 10(14) molecules cm(-2). Under humidified conditions (RH >10%), adsorbed water on the surface of the carbonate particles participates in the surface reactivity of these particles, which results in the enhanced uptake kinetics and extent of reaction of this organic acid on CaCO(3) as well as opens up several new reaction pathways. These reaction pathways include: (i) the water-assisted dissociation of carbonic acid to CO(2) and H(2)O and (ii) the formation of calcium formate islands and crystallites, as evident by SEM images. The results presented here show that adsorbed water plays a potentially important role in the surface chemistry of gas-phase organic acids on calcium carbonate particles.