The dynamics of electric field-induced transient birefringence Deltan(t) and light scattering (detected as turbidity) of 190 nm diameter unilamellar vesicles of dioleoylphosphatidylcholine are investigated as a function of applied field strength E, length of the square pulse Deltat, lipid concentration, mean hydrodynamic diameter , ionic strength, and temperature. Generally, induced birefringence exclusively is observed at low lipid concentration and below certain threshold values of E and Deltat, whereas concomitant induced turbidity appears at high lipid concentration and above thresholds values of E and Deltat. Turbidity is monitored through the change in transmitted intensity DeltaS parallel(t) and DeltaS perpendicular(t) of light polarized parallel and perpendicular to the applied field E. The field-induced structural changes are reflected in double-exponential forward relaxation and triple-exponential reverse relaxation of the positive birefringence, and in non-exponential relaxations of DeltaS parallel (t) and DeltaS perpendicular(t). Under the field, the associated physical events are interpreted as elongation of the spherical bilayer shells in the direction of E, linear chain formation (pearling) of the induced dipolar liposomes parallel to E, and partial fusion of adjoining vesicles within the chains. Under conditions where electroporation can be detected, pore opening succeeds the elongation of the vesicles. After termination of the field, the vesicles return to their original time average spherical shape, the oriented chains randomize and disintegrate, and the fused structures are converted either to unilamellar or multilamellar vesicles.
Metallodendrimers with ten chiral Ru centers have been prepared in a stereospecific fashion (see picture; *=chiral Ru(diimine)(3) center). These molecules are conformationally rigid and exhibit well-defined global topologies: some diastereomers exhibit macroscopically chiral structures, others show a disklike topology. This difference in global or tertiary structure is exemplified by differences in their colloidal behavior, as observed in electric birefringence measurements.
Electric field-induced transient birefringence and light scattering are reported for aqueous suspensions of synthetic unilamellar bilayer vesicles, prepared from the lipid dioleoylphosphatidylcholine (DOPC). The multiexponential birefringence relaxations observed on the microsecond and millisecond timescales are interpreted in terms of elongation and reorientation of induced dipolar vesicles, their linear chain formation, and electrofusion (and possibly electroporation) of the vesicles. Above certain threshold values of vesicle concentration, field-induced light scattering occurs concomitant with the birefringence. The corresponding transient signals corroborate the linear chain formation and subsequent fusion of the induced dipolar vesicles.
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