TCRT October 2011

category image Volume 10
No.5 (391-504)
October 2011
ISSN 1533-0338
Electropermeabilization

Identification of In Vitro Electropermeabilization Equivalent Pulse Protocols (465-473)

Exposure of cells to an external sufficiently strong electric field results in the formation of pores across the membrane. This phenomenon, termed electropermeabilization, permits the transport of poorly permeant molecules into cytosol. In clinical practice, cell membrane permeabilization for drug electrotransfer is achieved using the ESOPE pulse protocol (1000 V/cm, 8 pulses, 100 μs, 5 kHz). The aim of this study was to investigate several combinations of electric field amplitude and pulse number able to induce electropermeabilization as the one observed when the ESOPE protocol was applied. Decreasing electric field amplitudes (1000 to 300 V/cm) in combination with increasing number of pulses (8 to 320) were applied to in vitro MG63 cells. Propidium iodide and Calcein blue AM uptake were used to evaluate cell electropermeabilization and viability. Results showed that the threshold of local electric field needed to obtain electropermeabilization decreased exponentially with increasing the number of pulses delivered (r2 5 0.92, p < 0.0001). The absorbed dose threshold was dependent on the number of pulses for each voltage applied (r2 5 0.96, p < 0.0001). In conclusion, the possibility of applying an increased number of pulses rather than increasing the electric field amplitude to perform electropermeabilization, may become an important tool for electropermeabilization – related clinical applications.

Key words: In vitro electropermeabilization; Electric field amplitude; Pulse number; ESOPE pulse protocol.

This article can be cited as:
Ongaro, A., Pellati, A., Caruso, A., Battista, M., De Terlizzi, R., De Mattei, M., Fini, M. Identification of In Vitro Electropermeabilization Equivalent Pulse Protocols Technol Cancer Res Treat. 10, 465-473 (2011).

A. Ongaro, Ph.D.1*
A. Pellati, B.S.1
A. Caruso, Ph.D.1
M. Battista, Ph.D.2
F. De Terlizzi, Ph.D.2
M. De Mattei, Ph.D.1
M. Fini, M.D.3

1Department of Morphology and Embryology, University of Ferrara, Via Fossato di Mortara 64/B, 44121 Ferrara, Italy
2Laboratory of Clinical Biophysics, IGEA, Carpi, Italy
3Laboratory of Preclinical and Surgical Studies, Research Institute Codivilla Putti, Rizzoli Orthopaedic Institute Bologna, Italy

ngrlss@unife.it

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