Atomic form-factor measurements in the low-momentum transfer region for Li, Be, and Al by inelastic x-ray scattering

2008 ◽  
Vol 77 (6) ◽  
Author(s):  
A. Alatas ◽  
A. H. Said ◽  
H. Sinn ◽  
G. Bortel ◽  
M. Y. Hu ◽  
...  
2014 ◽  
Vol 47 (1) ◽  
pp. 35-40 ◽  
Author(s):  
Zoltán Varga ◽  
András Wacha ◽  
Attila Bóta

Time-resolved synchrotron small-angle X-ray scattering (SAXS) was used to study the structural changes during the osmotic shrinkage of a pharmacologically relevant liposomal drug delivery system. Sterically stabilized liposomes (SSLs) with a diameter of 100 nm and composed of hydrogenated soy phosphocholine, cholesterol and distearoyl-phosphoethanolamine-PEG 2000 prepared in a salt-free buffer were mixed with a buffered 0.3 MNaCl solution using a stopped flow apparatus. The changes in the liposome size and the bilayer structure were followed by using SAXS with a time resolution of 20 ms. A linear decrease in liposome size is observed during the first ∼4 s of the osmotic shrinkage, which reveals a water permeability value of 0.215 (15) µm s−1. The change in the size of the liposomes upon the osmotic shrinkage is also confirmed by dynamic light scattering. After this initial step, broad correlation peaks appear on the SAXS curves in theqrange of the bilayer form factor, which indicates the formation of bi- or oligolamellar structures. Freeze-fracture combined with transmission electron microscopy revealed that lens-shaped liposomes are formed during the shrinkage, which account for the appearance of the quasi-Bragg peaks superimposed on the bilayer form factor. On the basis of these observations, it is proposed that the osmotic shrinkage of SSLs is a two-step process: in the initial step, the liposome shrinks in size, while the area/lipid adapts to the decreased surface area, which is then followed by the deformation of the spherical liposomes into lens-shaped vesicles.


2007 ◽  
Vol 75 (6) ◽  
Author(s):  
Alexey Bosak ◽  
Michael Krisch ◽  
Irmengard Fischer ◽  
Simo Huotari ◽  
Giulio Monaco

1993 ◽  
Vol 48 (1-2) ◽  
pp. 283-288 ◽  
Author(s):  
A. Berthold ◽  
K.-J. Gabriel ◽  
W. Schülke

Abstract The dynamic structure factor S(q, ω) of electrons in lithium-intercalated graphite (LiC6) and potassium-intercalated graphite (KC8) for momentum transfer q || c-axis has been measured by inelastic synchrotron X-ray scattering. The dielectric function ε(q, ω) was deduced from the data and compared with ε(q, ω) of pristine graphite.The main feature in the different Im [ε(q, ω)]-spectra, a more or less intense peak around 14 eV, can be assigned to maxima of the symmetry-projected joint density of occupied and unoccupied electron states near the Fermi level. Knowing the position of the occupied bands by photoemission experiments, predictions about the unoccupied π and interlayer states can be made.In the case of LiC6 , a shift and broadening of the first Im [ε(q, ω)]-peak was found, which can be explained by a decrease of the energy of the interlayer-band because of the strong hybridization of this graphite-derived band with the Li metal 2s-band.In the case of KC8 , a weakening of the first peak of Im [ε(q, ω)] was observed, which we attribute both to a decreasing overlap of the occupied s-derived state with the empty interlayer state and to a change of symmetry of the occupied π-derived states as well as of the empty rc-derived states.


2005 ◽  
Vol 38 (1) ◽  
pp. 126-131 ◽  
Author(s):  
Michael R. Brzustowicz ◽  
Axel T. Brunger

An improved small-angle X-ray scattering (SAXS) method for determining asymmetric lipid bilayer structure in unilamellar vesicles is presented. From scattering theory, analytic expressions are derived for the bilayer form factor over flat and spherical geometries, assuming the lipid bilayer electron density to be composed of a series of Gaussian shells. This is in contrast to both classic diffraction and Guinier hard-shell SAXS methods which, respectively, are capable only of ascertaining symmetric bilayer structure and limited-resolution asymmetric structure. Using model fitting and direct calculation of the form factor, using only one equation, an asymmetric electron density profile of the lipid vesicle is obtained with high accuracy, as well as the average radius. The analysis suggests that the inner leaflet of a unilamellar lipid vesicle is `rougher' than the outer one.


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