Electroporation in dense cell suspension—Theoretical and experimental analysis of ion diffusion and cell permeabilization

Electroporation is a process where increased permeability of cells exposed to an electric field is observed. It is used in many biomedical applications including electrogene transfection and electrochemotherapy. Although the increased permeability of the membrane is believed to be the result of pore...

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Published inBiochimica et biophysica acta Vol. 1770; no. 1; pp. 12 - 23
Main Authors Pavlin, Mojca, Leben, Vilko, Miklavčič, Damijan
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 2007
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ISSN0304-4165
0006-3002
1872-8006
DOI10.1016/j.bbagen.2006.06.014

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Summary:Electroporation is a process where increased permeability of cells exposed to an electric field is observed. It is used in many biomedical applications including electrogene transfection and electrochemotherapy. Although the increased permeability of the membrane is believed to be the result of pores due to an induced transmembrane voltage U m, the exact molecular mechanisms are not fully explained. In this study we analyze transient conductivity changes during the electric pulses and increased membrane permeability for ions and molecules after the pulses in order to determine which parameters affect stabilization of pores, and to analyze the relation between transient pores and long-lived transport pores. By quantifying ion diffusion, fraction of transport pores f per was obtained. A simple model, which assumes a quadratic dependence of f per on E in the area where U m > U c very accurately describes experimental values, suggesting that f per increases with higher electric field due to larger permeabilized area and due to higher energy available for pore formation. The fraction of transport pores increases also with the number of pulses N, which suggest that each pulse contributes to formation of more and/or larger stable transport pores, whereas the number of transient pores does not depend on N.
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ISSN:0304-4165
0006-3002
1872-8006
DOI:10.1016/j.bbagen.2006.06.014