The interaction of nanosecond duration pulsed electric fields (nsPEFs) with biological cells, and the models describing this behavior, depend critically on the electrical properties of the cells being pulsed. Here, we used time domain dielectric spectroscopy to measure the dielectric properties of Jurkat cells, a malignant human T-cell line, before and after exposure to five 10 ns, 150 kV/cm electrical pulses. The cytoplasm and nucleoplasm conductivities decreased dramatically following pulsing, corresponding to previously observed rises in cell suspension conductivity. This suggests that electropermeabilization occurred, resulting in ion transport from the cell's interior to the exterior. A delayed decrease in cell membrane conductivity after the nsPEFs possibly suggests long-term ion channel damage or use dependence due to repeated membrane charging and discharging. This data could be used in models describing the phenomena at work. Ó 2007 Elsevier Inc. All rights reserved.Keywords: Dielectric spectroscopy; Nanosecond pulsed electric fields; Electroporation; Permeabilization; Plasma membrane; Time domain; Intracellular manipulation; Ultrashort pulsesThe permeability of the cell membrane to external molecules can be dramatically increased by applying pulsed electric fields (PEFs) above a threshold voltage [1]. The mechanism behind this electropermeabilization is electroporation, or pore formation in the cell membrane, and usually occurs for PEFs with electric fields on the order of a few kV/cm and pulse durations on the order of 0.1-10 ms. With the appropriate combination of these parameters, electroporation is irreversible and the membrane breaks down, which is desirable for applications ranging from bacterial decontamination to food processing [2]. Many applications require temporarily opening the cell membrane to normally impermeant molecules, such as electrochemotherapy and gene therapy [3]. Applying pulses with higher field strength (50-300 kV/cm) and shorter duration (10-300 ns) do not fully charge the cell membrane and instead interact primarily with the membranes of intracellular organelles [4]. These nanosecond duration PEFs (nsPEFs) cause intracellular calcium release [5,6] and apoptosis-induction in cell suspensions and in vivo tumors [5,7,8]. To better understand the mechanisms involved, attempts to develop mathematical models are underway 0006-291X/$ -see front matter Ó