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E M Egorova

Publications and source records attributed to E M Egorova.

6 recordsLinked to original sources

The relaxation effect as observed on lipid suspensions of low polydispersity.

Lipid suspensions with a low polydispersity (delta = 0.15 +/- 0.05, as given by photon correlation spectroscopy (PCS)) were used to elucidate the origin of the disagreement between the experimental zeta potential values (zeta sm), obtained from the electrophoretic mobilities through the Smoluchowski equation, and double-layer theory prediction (zeta potential) at low salt concentrations. The values of zeta sm, measured for cardiolipin and phosphatidylserine suspensions in monovalent electrolytes, were compared with the correspondent theoretical values of the zeta potentials correlated for the relaxation effect; the correction was made according to the S.S. Dukhin theory of electrophoresis. It was found, that this correction eliminates the disagreement for cardiolipin in NaCl entirely; it partly solves the problem for cardiolipin in KCl but fails to improve the situation for phosphatidylserine in NaCl.

Animals

Some problems of zeta potential determination in electrophoretic measurements on lipid membranes.

Electrophoretic mobilities were measured for cardiolipin, phosphatidylinositol and phosphatidylserine liposomes in solutions of potassium chloride. The zeta potential as a function of ionic strength deviates significantly from the predictions of the double-layer theory in the 10(-3)-5.10(-2) M range. This might be due to changes in pH in the course of the experiment and/or to the inapplicability of the Smoluchowski equation at low ionic strengths. Taking into account the relaxation effects results in theoretical curves, calculated for various particle sizes at low ionic strength, which are in better agreement with the experiment. However, for quantitative comparison with experimental data, further investigations are necessary.

Cardiolipins

[Studies of complex lipids. Synthesis of ionophore derivatives of diphosphatidylglycerol (cardiolipin)].

Synthesis of cardiolipin analogues containing an ionophore residue in the fatty acid moiety is described. The ionophore, dibenzo-18-crown-6, has been incorporated into second position of the glycerol residue by acylating mono- and dilysocardiolipin with a modified fatty acid anhydride. Lyso-derivatives of cardiolipin have been prepared by enzymatic hydrolysis of beef heart cardiolipin by snake venom phospholipase A2 (Naja naja oxiana).

Acylation