High-speed imaging of giant unilamellar vesicles (GUVs)
in recent
years has shown significant shape deformation of these vesicles under
electroporating direct current (DC) pulsed electric fields, possibly
altering the surface distribution of transmembrane potential (TMP)
and, thereby, the location and extent of electroporation on the bilayer
membrane. The development of TMP, the corresponding shape deformation,
and the extent of electroporation depend upon the waveform of the
applied electric field. In this work, the deformation of vesicles
was carried out under a high-intensity, single cycle of a sinusoidal
pulsed electric field (SSPEF) and a square wave pulsed electric field
(SWPEF). The cylindrical shape deformations of vesicles were observed
for both SSPEF and SWPEF and were dependent upon the ratio of conductivity
of the inner medium to the outer medium, α. For α = 1
and α > 1, the vesicles deformed into prolate cylinders as
a
result of Maxwell stress, whereas they were compressed into oblate
cylinders for α < 1. Vesicles subjected to a SSPEF relaxed
following either the pore closure dominated t
2 or the efflux and lipid loss dominated, slow t
3 mechanism depending upon the value of α. For α
= 1 and α < 1, the relaxation of the vesicles was found to
be predominantly dependent upon pore closure. On the other hand, a
majority of vesicles gained excess area during poration when α
> 1, which can be attributed to a higher TMP and faster charging
of
the membrane. The predictions of the approximate model for the deformation
of vesicles agreed with the experiment, with deviations between the
two as a result of the simplicity of the model. Moreover, the degree
of deformation of vesicles [measured by the aspect ratio (AR)] and
shape deformations of vesicles were found to be dependent upon the
pulse width (T
P) and amplitude (E
0) of the SSPEF. The specific temporal variation
of pore-forming tendencies of SSPEF and SWPEF, with their associated
peculiarities, can be judiciously used for controlling electroporation
in cells and vesicles.