5,041 research outputs found
Saturated Anionic Phospholipids Enhance Transdermal Transport by Electroporation
AbstractAnionic phospholipids, but not cationic or neutral phospholipids, were found to enhance the transdermal transport of molecules by electroporation. When added as liposomes to the milieus of water-soluble molecules to be delivered through the epidermis of porcine skin by electroporation, these phospholipids enhance, by one to two orders of magnitude, the transdermal flux. Encapsulation of molecules in liposomes is not necessary. Dimyristoylphosphatidylserine (DMPS), phosphatidylserine from bovine brain (brain-PS), dioleoylphosphatidylserine (DOPS), and dioleoylphosphatidylglycerol (DOPG) were used to test factors affecting the potency of anionic lipid transport enhancers. DMPS with saturated acyl chains was found to be a much more potent transport enhancer than those with unsaturated acyl chains (DOPS and DOPG). There was no headgroup preference. Saturated DMPS was also more effective in delaying resistance recovery after pulsing, and with a greater affinity in the epidermis after pulsing. Using fluorescent carboxyl fluorescein and fluorescein isothiocyanate (FITC)-labeled Dextrans as test water-soluble molecules for transport, and rhodamine-labeled phospholipids to track anionic phospholipids, we found, by conventional and confocal fluorescence microscopy, that transport of water-soluble molecules was localized in local transport spots or regions (LTRs) created by the electroporation pulses. Anionic phospholipids, especially DMPS, were located at the center of the LTRs and spanned the entire thickness of the stratum corneum (SC). The degree of saturation of anionic phospholipids made no difference in the densities of LTRs created. We deduce that, after being driven into the epidermis by negative electric pulses, saturated anionic phospholipids mix and are retained better by the SC lipids. Anionic lipids prefer loose layers or vesicular rather than multilamellar forms, thereby prolonging the structural recovery of SC lipids to the native multilamellar form. In the presence of 1mg/ml DMPS in the transport milieu, the flux of FITC-Dextran-4k was enhanced by 80-fold and reached 175μg/cm2/min. Thus, the use of proper lipid enhancers greatly extends the upper size limit of transportable chemicals. Understanding the mechanism of lipid enhancers enables one to rationally design better enhancers for transdermal drug and vaccine delivery by electroporation
Phonon Effects on Spin-Charge Separation in One Dimension
Phonon effects on spin-charge separation in one dimension are investigated
through the calculation of one-electron spectral functions in terms of the
recently developed cluster perturbation theory together with an optimized
phonon approach. It is found that the retardation effect due to the finiteness
of phonon frequency suppresses the spin-charge separation and eventually makes
it invisible in the spectral function. By comparing our results with
experimental data of TTF-TCNQ, it is observed that the electron-phonon
interaction must be taken into account when interpreting the ARPES data.Comment: 5 pages, 5 figures, minor differences with the published version in
Physical Review Letter
Evidence for Two Gaps and Breakdown of the Uemura Plot in BaKFeAs Single Crystals
We report a detailed investigation on the lower critical field of
the superconducting BaKFeAs (FeAs-122) single crystals.
A pronounced kink is observed on the curve, which is attributed to
the existence of two superconducting gaps. By fitting the data to
the two-gap BCS model in full temperature region, a small gap of
meV and a large gap of meV
are obtained. The in-plane penetration depth is estimated to
be 105 nm corresponding to a rather large superfluid density, which points to
the breakdown of the Uemura plot in FeAs-122 superconductors.Comment: 5 pages, 4 figure
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