Synthesis and characterization of fluorescein isothiocyanate (FITC)-labeled PEO-PCL-PEO triblock copolymers for topical delivery

We present the synthesis of fluorescein isothiocyanate (FITC)-labeled poly(ethylene oxide)-block-poly(?-caprolactone)-block-poly(ethylene oxide) (PEO-PCL-PEO) triblock copolymers and their applications for tracking the penetration behavior of FITC-labeled copolymers in the hairless mouse skin. In the first step, PEO-PCL diblock copolymers with different ratios of PCL to PEO (i.e., [CL]/[EO]) were prepared by ring opening polymerization of ?-caprolactone (CL), where monomethoxy poly(ethylene glycol) (mPEG, M_n = 2000 g mol⁻¹) was used as a macro-initiator. FITC was successively reacted with octadecylamine, isophorone diisocyanate (IPDI), and then used as a linker to obtain PEO-PCL-PEO triblock copolymers from the PEO-PCL diblock copolymers. In aqueous solution, both FITC-labeled triblock copolymers show two UV absorption peaks at 489 and 455 nm, attributed to the monomeric FITC and H-aggregated FITC moieties, respectively. Due to the strong H-aggregation of FITC in the copolymer of high [CL]/[EO], fluorescent emission intensities considerably decreased at high concentrations of the copolymer. FITC-labeled copolymers exhibited more sharper polarized optical and fluorescence microscopic images compared to the mixtures of FITC and unlabeled copolymer in both solid crystalline and multiple emulsion state. Furthermore, the Frantz diffusion cell test was carried out to demonstrate the penetration behavior of the FITC-labeled copolymers in the hairless mouse skin.     

Membrane electrode assemblies doped with H3PO4 for high temperature proton exchange membrane fuel cells

H₃PO₄ content plays a critical role in high temperature proton exchange membrane fuel cells (HT-PEMFC), as it is responsible for the majority of the conductivity of the key components under high temperature operation. The conductivities of commercial AB-PBI membranes doped by immersing in 85 wt.% H₃PO₄ for different times and temperatures are investigated. The effect of H₃PO₄ loading in electrodes, including the AB-PBI polymer and a Pt/C catalyst, is also studied. The as-prepared electrodes and membranes are combined to fabricate a membrane electrode assembly for HT-PEMFCs. The results reveal that AB-PBI membranes doped with 85 wt.% H₃PO₄ at 90 °C for 9 h display a maximum conductivity of 33 mS cm⁻¹. This membrane was selected and combined with electrodes including 15 wt.% AB-PBI and 0.75 mg cm⁻² Pt with different H₃PO₄ loadings. A maximum current density of 260 mA cm⁻² was achieved in the as-prepared MEA (with 5 mg cm⁻² H₃PO₄ in electrodes) operating at 0.6 V and 160 °C, using oxygen and hydrogen.     

Effect of succinic anhydride as an electrolyte additive on electrochemical characteristics of silicon thin-film electrode

The effect of an electrolyte additive, succinic anhydride (SA), on the electrochemical performances of a silicon thin-film electrode, which is prepared by radio-frequency magnetron sputtering, is investigated. The introduction of SA into a liquid electrolyte consisting of ethylene carbonate/diethyl carbonate/1 M LiPF₆ significantly enhances the capacity retention and coulombic efficiency of the electrode. This improvement in the electrochemical performance of the electrode is attributed to modification of the solid/electrolyte interphase (SEI) layer by the introduction of SA. The differences in the characteristic properties of SEI layers, with or without SA, are explained by analysis with scanning electron microscopy, electrochemical impedance spectroscopy, and X-ray photoelectron spectroscopy.     

Synthesis of trideuteratedO-alkyl platelet activating factor and lyso derivatives

Racemic heavy isotope analogs of 1-O-alkyl-sn-glycero-3-phosphocholine (lysoPAF) and 1-O-alkyl-2-O-acetyl-sn-glycero-3-phosphocholine (PAF) were prepared for use as internal standards to facilitate quantitative studies based on mass spectrometry. Starting from pentadencane-1,15-diol andrac-glycerol-1,2-acetonide, a convergent synthesis of 1-O-[16′-²H₃]hexadecyl and 1-O-[18′-²H₃]octadecylrac-glycero-3-phosphocholine and their acetyl derivatives is described. Three deuterium atoms were introduced at the terminal position of the 1-O-alkyl group by displacement of thep-toluensulfonyl group from 1-O-alkyl-15′-p-toluensulfonate and 1-O-alkyl-17′-p-toluensulfonate with [²H₃]-methylmagnesium iodide. The 1-O-alkyl-17′-p-toluensulfonate was obtained by reaction of the 1-O-alkyl-15′-p-toluensulfonate with allylmagnesium bromide, followed by reductive ozonolysis and treatment withp-toluenesulfonyl chloride. The hydroxyl group at C-2 was protected by a benzyl group and removed at a late stage in the synthesis. This provided the corresponding lysoderivatives or allowed preparation of racemic PAF by subsequent acetylation of the free hydroxy group. The phosphocholine moiety was introduced at glycerol C-3 by reaction with bromoethyldichlorophosphate and trimethylamine. The synthetic compounds were analyzed by FAB/MS and GC/NICIMS. They were shown to contain less than 0.6% protium impurity.     

Fatty chain compositon of ether and ester glycerophospholipids in the Japanese oysterCrassostrea gigas (Thunberg)

The fatty chain compositions of 1-O-alk-1′-enyl-2-acyl, 1-0-alkyl-2-acyl, and 1,2-diacyl glycerophospholipids of the Japanese oysterCrassostrea gigas (Thunberg) were investigated. Major fatty chains in thesn-1 position of 1-alk-1′-enyl-2-acyl ethanolamine phospholipids (EPL) were 18∶0 (64.7%) and 20∶1 (11.1%). Majorsn-1 chains of alkenylacyl choline phospholipids (CPL) were 18∶0 (63.3%) and 16∶0 (22.2%). In the case of 1-alkyl-2-acyl EPL, the predominant fatty chains in thesn-1 position were 18∶0 (51.5%), 16∶0 (16.0%) and 20∶1 (12.5%); in the case of 1-alkyl-2-acyl CPL, the majorsn-1 chains were 16∶0 (44.0%) and 14∶0 (23.4%). Saturated fatty chains were predominant in both EPL and CPL. Prominent fatty acids in thesn-2 position of the alkenylacyl EPL were 22∶6n−3 (29.0%), 20∶5n−3 (19.0%) and 22∶2 NMID (non-methylene interrupted dienes, 16.6%) contributing to about 65% of the total fatty acids, while alkenylacyl CPL was rich in the saturated acids 16∶0 (32.0%) and 18∶0 (9.2%). In the alkylacyl EPL, 16∶0, 18∶1n−9, 18∶0 and 16∶1n−7 were prominentsn-2 fatty acids and accounted for 30.6%, 10.0%, 9.8%, and 8.3%, respectively. Polyunsaturated fatty acids were detected, but were present at extremely low percentages. Majorsn-2 fatty acids in alkylacyl CPL were 16∶0 (25.4%), 22∶6n−3 (16.0%) and 20∶5n−3 (8.4%). The major fatty acids of diacyl EPL were 20∶5n−3 (22.3%), 16∶0 (17.9%), and 18∶0 (16.1%), and those of diacyl CPL were 16∶0 (30.4%), 20∶5n−3 (17.6%) and 18∶1n−7 (7.4%).     

Coal combustion characteristics in a circulating fast fluidized bed

The effect of coal size (0.73–1.03 mm), excess air ratio (1.0–1.4), operating bed temperature (750–900‡C), coal feeding rate (1–3 kg/h), and coal recycle rate (20–40 kg/h) on combustion efficiency, temperature profiles along the bed height and flue gas composition have been determined in a bubbling and circulating fluidized bed combustor (7.8 cm-ID x 2.6 m-high). Combustion efficiency increases with increasing excess air ratio and operating bed temperature and it decreases with increasing particle size in the bubbling and circulating fluidzing beds. In general, temperature profiles and combustion efficiency are more uniform and higher in a circulating bed than those in bubbling bed. Combustion efficiency also increases with increasing recycle rate of unburned coal in the circulating bed. The ratio of CO/CO₂ of flue gas decreases with increasing bed temperature and excess air ratio, whereas the ratio of O₂(CO + CO₂) decreases with bed temperature in both bubbling and circulating fluidized beds.     

Effect of various phenol additives on viscosity of SRC blends

Coal-derived liquids are susceptible to oxidative degradation. Two different weight ratios of SRC-I/SRC-II blends, with or without phenol derivatives, have been subjected to accelerated ageing studies. Viscosity, infrared, elemental analysis, molecular weight determination, and solvent analysis are used to examine the properties of the degradation products. On ageing, there is a large increase in the amount of toluene-insoluble material, decrease in oil components, and a relatively constant amount of asphaltenes. The oxygen content increases in the aged toluene-insoluble and asphaltene fractions, and a new absorption at ≈1700 cm^?1 (the C = 0 group) appears in these two fractions only. On the addition of phenol itself and the less hindered phenol derivatives, the original hydrogen-bonding between the acidic and basic fuctional groups in the coal liquids is apparently disrupted because the added phenol can now interact with the proton-accepting species in the liquids, thus leading to a lower viscosity. This does not mean that the unhindered phenols retard the rate of ageing. The original hydrogen-bonding in the coal-derived liquid now gives way to a new hydrogen-bonding, and ageing occurs with the latter. The more hindered phenol derivatives are not as effective as phenol in disrupting the original hydrogen-bonding in the coal-derived liquids.     

R-Curve Behavior of Si3N4–BN Composites

R -curve behavior of Si₃N₄–BN composites and monolithic Si₃N₄ for comparison was investigated. Si₃N₄–BN composites showed a slowly rising R -curve behavior in contrast with a steep R -curve of monolithic Si₃N₄. BN platelets in the composites seem to decrease the crack bridging effects of rod-shaped Si₃N₄ grains for small cracks, but enhanced the toughness for long cracks as they increased the crack bridging scale. Therefore, fracture toughness of the composites was relatively low for the small cracks, but it increased significantly to ∼8 MPa·m^1/2 when the crack grew longer than 700 μm, becoming even higher than that of the monolithic Si₃N₄.     

Thickness and composition dependence of the glass transition temperature in thin random copolymer films

Glass transition temperatures (T_g) of thin poly(styrene-co-methyl methacrylate) and poly(2-vinyl pyridine-co-styrene) films coated on a native oxide surface of Si wafer (100) were measured by ellipsometry. The thickness dependence of T_g can be properly fitted by previously suggested equation developed for homopolymers, based upon a continuous multi-layer model, although one component in thin random copolymer films demonstrates a slightly favorable interaction between a substrate and thin film, and another demonstrates a strongly favorable interaction. Surface and interface have a strong influence on T_g of thin film coated on substrate: the surface has the effect of reducing T_g, whereas the interface increases the T_g according to the degree of interaction between a substrate and thin film. This degree of interaction can be quantified as an interaction parameter (k), and is dependent on the composition of random copolymers. For the estimation of k values of thin random copolymer films, we proposed a parallel type additive function (1/k_ran=w₁/k₁+w₂/k₂) where w is a weight fraction of component.