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EN
In this paper, the effects of model (commercial) and natural (extracted from peat) humic substances on the membrane of liposomes formed with egg yolk lecithin (EYL) are presented. In our research, mass concentrations of fulvic and humic acids were used, which in relation to lecithin varied from 0% to 13%. To study membrane fluidity, electron spin resonance (EPR) was used with two spin probes, penetrating various regions of the lipid bilayer. The effects of model and natural humic substances (humic acids – HAs and fulvic acids – FAs) on the lipid membrane in different regions were researched: the lipid-water interphase, and in the middle of the lipid bilayer. It was shown that FA and HA impact the fluidity of liposome membranes in different ways. Increased mass concentrations of HAs decreased membrane fluidity in both acids: extracted from peat and the model. However, increased mass concentration of FAs extracted from peat, decreased membrane fluidity in the surface region, at the same time stiffening the central part of the bilayer. Increasing the concentration of FAs extracted from peat had the opposite effect when compared to model FA. This effect may be related to the complexation of xenobiotics present in the soil environment and their impact on biological membranes.
EN
In this work the changes in the fluidity of liposome membranes caused by alanine and butyrine derivatives (Ac-Ala-NMe2 and Ac-Abu-NMe2) were investigated. Liposomes were obtained in the process of egg yolk lecithin (EYL) sonication. The concentration of the admixture in the proportion to EYL varied from 0 to 25% mole. The electron spin resonance (ESR) spectroscopy was used with two different spins probes. Each spin probe penetrates different regions of liposome membrane. The TEMPO probe occurs both in the hydrophobic part of the membrane and in the water environment what allows to determine the spectroscopic parameter F of division of this probe into the membrane and its water surrounding. DOXYL is localized in the central part of the lipid bilayer and is used to obtain the spectroscopic parameter τ – rotation correlation time – whose value gives information about fluidity changes in the middle of the lipid bilayer. The study indicated that the tested as admixtures N-methylated model peptides significantly changed the fluidity of liposome membranes. The dynamic of this process depends both on amino acids derivative and on the membrane region. Both studied compounds increased the fluidity of the surface layer of liposome membrane. At the same time, butyrine derivative caused the stiffening of the middle part of liposome bilayer, but alanine derivative slightly increased the fluidity of this region.
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