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Application of spin markers for study of liposome prepared by the modified reverse-phase evaporation method.

Authors :
Pentak, Danuta
Sułkowski, Wiesław W.
Wolińska, Agnieszka
Maślanka, Sławomir
Bojko, Barbara
Maciążek, Małgorzata
Równicka, Joanna
Sułkowska, Anna
Source :
Spectroscopy: An International Journal. 2008, Vol. 22 Issue 1, p33-41. 9p. 4 Diagrams, 1 Chart, 3 Graphs.
Publication Year :
2008

Abstract

The EPR spectroscopy was used to determine the structure and physicochemical properties of liposomes prepared from L-α-phosphatidylcholine dipalmitoyl (DPPC) by the modified reverse-phase evaporation method (mREV). EPR study was carried out in the temperature range from 297 K to 340 K i.e. below and above the phase transition temperature TC of DPPC. On the basis of EPR spectra of spin marker 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) incorporated into the liposome, the parameter f was determined. TEMPO dissolves easily in water and in the fluid lamellar smectic liquid-crystaline phase of lipid bilayer but is largely excluded from the solid, gel-phase. Thus TEMPO can be used to observe the change in the partition between aqueous and fluid lipid regions. The change in the relative value of f as a function of temperature for DPPC shows that, in the presence of water excess, this phospholipids undergoes a transition from a “gel phase” to a lamellar smectic liquid crystalline phase. On the basis of EPR spectra of spin marker 2-(3carboxypropyl)-4,4-dimethyl-2-tridecyl-3-oxazolidinloxyl (5-DOXYL) incorporated into liposome, the parameter a′N was determined. The isotropic 14N-hyperfine coupling constant a′N of nitroxide spin label depends on the local environmental polarity. The increase of a′N value reflects the rise of polarity of spin label environment. Temperature, cholesterol and pH dependent structural changes were also described. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07124813
Volume :
22
Issue :
1
Database :
Academic Search Index
Journal :
Spectroscopy: An International Journal
Publication Type :
Academic Journal
Accession number :
31547199
Full Text :
https://doi.org/10.1155/2008/505818