Fabrication of Wettability-Patterned Surface for Cellular Micropatterning Using Step-Wise Ion Beam Processing.

In this study, the fabrication of a wettability patterned surface for cellular micropatterning was investigated using step-wise ion beam processing. A perfluorinated poly(ethylene-co-propylene) (FEP) film was first irradiated using accelerated Xe+ ions with 100 keV of energy at the low current density of 1 A/cm² over the entire surface. Second, its confined regions were irradiated at the higher current density of 15 A/cm² at various ion fluences through the pattern mask to generate patterns with big differences in wettability.

Electron beam-based fabrication of crosslinked hydrophilic carbon electrodes and their application for capacitive deionization.

In this research, we demonstrated that a crosslinked hydrophilic carbon electrode with better electrochemical performance than hydrophobic counterparts can easily be produced using room-temperature, quick electron-beam irradiation with a hydrophilic methacryloyl-substituted polyvinyl alcohol (SPVA) binder. The SPVA binder was effectively synthesized by trans-esterification of PVA with glycidyl methacrylate. The hydrophilic carbon electrode cast on a graphite sheet from a slurry of activated carbon (AC) and SPVA was irradiated with an electron beam to form a crosslinked structure.

Acid-labile mPEG-vinyl ether-1,2-dioleylglycerol lipids with tunable pH sensitivity: synthesis and structural effects on hydrolysis rates, DOPE liposome release performance, and pharmacokinetics.

A family of 3-methoxypoly(ethylene glycol)-vinyl ether-1,2-dioleylglycerol (mPEG-VE-DOG) lipopolymer conjugates, designed on the basis of DFT calculations to possess a wide range of proton affinities, was synthesized and tested for their hydrolysis kinetics in neutral and acidic buffers. Extruded ∼100 nm liposomes containing these constructs in ≥90 mol % 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE) produced dispersions that retained their calcein cargo for more than 2 days at pH 7.5, but released the encapsulated contents over a wide range of time scales as a function of the electronic properties of the vinyl ether linkage, the solution pH, and the mPEG-VE-DOG composition in the membrane.

Lance-adams syndrome.

It is not common for a patient who survives cardiac arrest to experience significant neurologic impairment such as acute and chronic post-hypoxic myoclonus, known as Lance-Adams syndrome. This syndrome is predominantly characterized by myoclonus that starts days to weeks after cardiopulmonary resuscitation in patients who regained consciousness. Although several cases of LAS were reported, the decisive treatment method has not been established.

The availability of radiological measurement of tibial torsion: three-dimensional computed tomography reconstruction.

Objective: To assess the intra-rater and inter-rater reliability for measuring tibial torsion measurements by a radiographic method using three-dimensional computed tomography reconstruction (3D-CT) and to compare the physical measures to those of 3D-CT.

Method: The study included 33 children who presented with intoeing gait. Tibial torsion was measured by 3D-CT.

Improved plasmalogen synthesis using organobarium intermediates.

An improved synthesis of plasmalogen type lipids is described. Transmetalation of lithioalkoxy allyl intermediates with BaI(2) and subsequent alkylation with 1-iodoalkanes enables the stereoselective formation of O-(Z)-alkenyl ether as precursors for the synthesis of plasmenyl- and bisplasmenylcholines. This method provides a simple and adaptable approach for the stereocontrolled synthesis of plasmenyl derivatives with variations at the sn-1, sn-2, and sn-3 positions of the glycerol backbone.

Acid-triggered release via dePEGylation of DOPE liposomes containing acid-labile vinyl ether PEG-lipids.

Four structurally related, acid-labile polyethylene glycol (PEG) conjugated vinyl ether lipids have been synthesized and used at low molar ratios to stabilize the nonlamellar, highly fusogenic lipid, dioleoylphosphatidyl ethanolamine, as unilamellar liposomes. Acid-catalyzed hydrolysis of the vinyl ether bond destabilized these liposomes by removal of the sterically-stabilizing PEG layer, thereby promoting contents release on the hours timescale at pH<5. Structure-property correlations of these compounds suggested that single vinyl ether linkages between the PEG headgroup and the lipid backbone produce faster leakage rates.

Direct synthesis of plasmenylcholine from allyl-substituted glycerols.

We report a new method for the facile preparation of plasmenylcholine via reaction of lithioalkoxy allyl intermediates with 1-iodoalkanes as the key step in the stereoselective formation of 1'-(Z)-alkenyl glyceryl ethers. The allyl anion intermediate is prepared by treating mono- or disiloxy-protected 1-allylglycerol precursors with s-BuLi at -65 to -80 degrees C. Subsequent addition of 1-iodoalkane solutions at low temperature gives moderate yields of gamma-coupled, Z-vinyl ethers as the major product and alpha-coupled product as the minor component.

Facile synthesis of plasmalogens via Barbier-type reactions of vinyl dioxanes and vinyl dioxolanes with alkyl halides in LiDBB solution.

Plasmalogens (i.e. plasmenylcholines or plasmenylethanolamines) are a biologically important class of glycerophospholipids that have been difficult to synthesize due to the presence of an acid and oxidatively labile (Z)-vinyl ether substituent at the sn-1 position and a base-labile sn-2 acyl substituent that easily migrates during silica gel purification.