| Nanosecond megavolts-per-meter pulsed electric field (nsPEF) offers a non-invasive manipulation of intracellular organelles and functions of biological cells. Accordingly, nsPEF is a potential technique for biophysical research and cancer therapy, and is of growing interest. Although, the application of nsPEF has shown electroperturbation on cell plasma membranes and intracellular membranes as well, the mechanisms underlying the electropermeabilization are still not clear. In this thesis, we systematically study nsPEFs (5 and 30 ns) induced membrane permeability change in biological cell in-vitro with different pulse parameters. In Chapter 3, we investigate the nsPEF-induced intracellular membrane permeabilization of mitochondria which play key roles in activating apoptosis in mammalian cells. The results show the evidences of nsPEF-induced membrane permeability increase in mitochondria, and suggest that nsPEF is a potential technology for cancer cell ablation without delivery of drug or gene into cells.;In Chapter 2, 4 and 6, we study the properties of nsPEF-induced plasma membrane permeabilization. In the beginning, the change of plasma membrane permeability is studied by uptake of YO-PRO-1 and propidium iodide, fluorescent dyes specifically used as indicators of plasma membrane permeabilization. However, the detection is limited by the fluorescent emission efficiency and detector capability. To increase the detection sensitivity, we later develop a method based on cell volume change due to regulation of osmotic balance that causes water and small ions transport through plasma membrane. We find that even a single 10 MV/m pulse of 5 ns duration produces measureable cell swelling. The results demonstrate that cell swelling is susceptible to nsPEF and can detect membrane permeabilization more easily and precisely than fluorescent dyes. We compare the effects of different pulse parameters (pulse duration, pulse number, electric field amplitude and pulse repetition rate) on electropermeabilization. The effects of chemical agents that either promote (H2O2) or inhibit (lanthanide ions and Hg2+) electropermeabilization are also studied. To characterize the population of pores created by nsPEFs, we isoosmotically substitute different size of neutral molecules in the pulsing medium, and estimate pore size by analyzing cell volume changes that result from the permeation of these substituted molecules through the plasma membrane of Jurkat T lymphoblasts. The basis of this method is regulation of osmotic balance across the plasma membrane as well. We find that most pores opened by 5-100 5 ns pulses in plasma memebrane of Jurkat T lymphoblasts have diameter between 0.7-0.9 nm.;In Chapter 5, we report the design and construction of a delivery system for nsPEF. We integrate a pair of delicately fabricated tungsten wire electrodes spaced 100 mum, a solid-state high-voltage nanosecond pulse generator and a fluorescent microscope coupling with a fast and sensitive digital recording camera. This system enables real-time biophotonic investigations of the nsPEF-induced biological responses of living mammalian cells in-vitro. |
