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1.
IEEE Trans Biomed Eng ; 58(11): 3279-88, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21900067

ABSTRACT

Electroporation-based applications require the use of specific pulse parameters for a successful outcome. When recommended values of pulse parameters cannot be set, similar outcomes can be obtained by using equivalent pulse parameters. We determined the relations between the amplitude and duration/number of pulses resulting in the same fraction of electroporated cells. Pulse duration was varied from 150 ns to 100 ms, and the number of pulses from 1 to 128. Fura 2-AM was used to determine electroporation of cells to Ca(2+). With longer pulses or higher number of pulses, lower amplitudes are needed for the same fraction of electroporated cells. The expression derived from the model of electroporation could describe the measured data on the whole interval of pulse durations. In a narrower range (0.1-100 ms), less complex, logarithmic or power functions could be used instead. The relation between amplitude and number of pulses could best be described with a power function or an exponential function. We show that relatively simple two-parameter power or logarithmic functions are useful when equivalent pulse parameters for electroporation are sought. Such mathematical relations between pulse parameters can be important in planning of electroporation-based treatments, such as electrochemotherapy and nonthermal irreversible electroporation.


Subject(s)
Electroporation/methods , Models, Biological , Animals , CHO Cells , Calcium/chemistry , Calcium/metabolism , Cricetinae , Cricetulus , Fluorescent Dyes/chemistry , Fluorescent Dyes/metabolism , Fura-2/chemistry , Fura-2/metabolism , Temperature
2.
Med Biol Eng Comput ; 48(5): 407-13, 2010 May.
Article in English | MEDLINE | ID: mdl-20361267

ABSTRACT

It has been reported previously that electric pulses of sufficiently high voltage and short duration can permeabilize the membranes of various organelles inside living cells. In this article, we describe electropermeabilization of endocytotic vesicles in B16 F1 mouse melanoma cells. The cells were exposed to short, high-voltage electric pulses (from 1 to 20 pulses, 60 ns, 50 kV/cm, repetition frequency 1 kHz). We observed that 10 and 20 such pulses induced permeabilization of membranes of endocytotic vesicles, detected by release of lucifer yellow from the vesicles into the cytosol. Simultaneously, we detected uptake of propidium iodide through plasma membrane in the same cells. With higher number of pulses permeabilization of the membranes of endocytotic vesicles by pulses of given parameters is accompanied by permeabilization of plasma membrane. However, with lower number of pulses only permeabilization of the plasma membrane was detected.


Subject(s)
Electroporation/methods , Melanoma, Experimental/metabolism , Transport Vesicles/metabolism , Animals , Cell Membrane/metabolism , Cell Membrane Permeability/physiology , Isoquinolines/pharmacokinetics , Mice , Propidium/pharmacokinetics , Tumor Cells, Cultured
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