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Biophys J, February 2001, p. 755-764, Vol. 80, No. 2

and
Schools of *Chemical and
Biomedical Engineering,
Georgia Institute of Technology, Atlanta, Georgia 30332, and
Department of Urology, Emory University School of
Medicine, Atlanta, Georgia 30322 USA
Electroporation's use for laboratory transfection and
clinical chemotherapy is limited by an incomplete understanding of the effects of electroporation parameters on molecular uptake and cell
viability. To address this need, uptake of calcein and viability of DU
145 prostate cancer cells were quantified using flow cytometry for more
than 200 different combinations of experimental conditions. The
experimental parameters included field strength (0.1-3.3 kV/cm), pulse
length (0.05-20 ms), number of pulses (1-10), calcein concentration (10-100 µM), and cell concentration (0.6-23% by volume). These data indicate that neither electrical charge nor energy was a good
predictor of electroporation's effects. Instead, both uptake and
viability showed a complex dependence on field strength, pulse length,
and number of pulses. The effect of cell concentration was explained
quantitatively by electric field perturbations caused by neighboring
cells. Uptake was shown to vary linearly with external calcein
concentration. This large quantitative data set may be used to optimize
electroporation protocols, test theoretical models, and guide
mechanistic interpretations.
Biophys J, February 2001, p. 755-764, Vol. 80, No. 2
© 2001 by the Biophysical Society 0006-3495/01/02/755/10 $2.00
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