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Plasma generated by the resistive barrier discharge has been used to efficiently inactivate pathogenic microorganisms and to destroy cancer cells. These biomedical applications of low temperature plasma are of great interest because in recent times bacteria developed increased resistance to antibiotics and because present cancer therapies often are accompanied by serious side effects. Low temperature plasma, such the one generated by the resistive barrier discharge, is a technology that can help overcome these healthcare challenges.
One of the most widely used approaches to generate low temperature atmospheric pressure plasmas is the dielectric barrier discharge (DBD). The dielectric barrier discharge original concept, which was first developed by Du Moncel in 1855[1], was further developed, improved, and its physics elucidated by several investigators [2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17]. In its most basic form the DBD uses a dielectric to cover one or two metal electrodes, which are separated by a small gas gap. The electrodes are driven by voltages of several kV at frequencies in the kHz range. Atmospheric pressure plasmas generated by DBDs have been extensively used in material processing, surface modification, as UV-VUV sources, as flow control actuators, the generation of ozone[18][19][20], and since the mid-1990s in biomedical applications[21].
One of the DBD limitations is that it needed to be operated with frequencies ranging from the kHz to the MHz. This required special high voltage power supplies at those frequencies, which added to the complexity of operating a DBD-based system. This shortcoming was overcome by replacing the dielectric barrier covering the electrodes by a high resistivity layer. Doing so allowed the extension of the frequency range all the way down to 0 Hz (DC)[22].
Few methods can be used to extend the operating frequency range of barrier discharges. One approach was the use of dielectric wire mesh electrode in a DBD to generate a glow discharge at a frequency of 50 Hz[23]. Laroussi and Alexeff developed another method to design a device that is known as the resistive barrier discharge (RBD)[22]. The RBD can be operated with DC or AC (50 or 60 Hz) power supplies. This discharge is somewhat similar to the DBD configuration, but instead of a dielectric barrier, a high resistivity (few MΩ.cm) sheet/layer is used to cover one of the electrodes (see Figure 1). The high resistivity sheet plays the role of a distributed resistive ballast, which helps avoid the discharge from localizing and inhibits the current from increasing to high values and turning the discharge into an arc. If helium gas was used and if the electrodes gap distance was below 5 cm, relatively uniform plasma could be maintained (see Figure 2). However, if air (>1%) was added to helium the discharge formed filaments which randomly appeared within the bulk of the volumetric plasma.
Figure 2. Photograph of the plasma generated by a resistive barrier discharge (RBD) in helium. The gap distance between the electrodes is 4.5 cm, and the voltage is 13 kV RMS at 60 Hz[22]. The input power is around 100 W.
The RBD can be operated under DC or AC excitation modes. Under both modes, the discharge current exhibits a series of pulses, suggesting that like the DBD, the RBD is also a self-pulsed discharge. Figure 3 shows a typical current characteristics (top waveform) under DC excitation and the corresponding light emission intensity (bottom waveform) detected by a photomultiplier tube (PMT). The current pulses are few microseconds wide and occur at a repetition rate of few tens of kHz. The pulsing of the discharge current can be explained by a combined resistive and capacitive model of the device. When the gas breaks down and a current of sufficient magnitude flows, the equivalent capacitance of the electrodes becomes charged to the point where most of the applied voltage appears across the resistive layer of the electrodes. The voltage across the gas gap then becomes insufficient to maintain gas breakdown. At this point, the equivalent capacitor discharges itself through the resistive layer. This results in a decrease of the voltage across the resistive layer and an increase in the voltage across the gas gap and breakdown occurs again. Figure 4 shows an electrical model of the RBD[24].
Figure 3. Current waveform (top curve) of a DC-powered (20 kV) RBD and discharge integrated light intensity detected by a photomultiplier tube (PMT) (curve is inverted to visually distinguish it from the current waveform). Note the correlation between the timing of the current and light pulses.
Figure 4. Electrical model of the RBD[24].
Since the mid-1990s low temperature plasma (LTP) has been used for various biomedical applications including the inactivation of bacteria, wound healing, and the destruction of cancer cells and tumors [21][25][26][27][28][29][30][31]. LTP was found to provide a rich cocktail of reactive species, such as reactive oxygen species, ROS, and reactive nitrogen species, RNS, that can interact with cells and tissues and induce biological effects[32]. The RBD offers a practical method to generate large volumes of low temperature atmospheric pressure plasma for many of the above-mentioned biomedical applications. The earliest work reported on the use of the RBD to inactivate bacteria [33][34][35][36][37].
Richardson et al. used the RBD to inactivate both Gram-negative and Gram-positive bacteria[33]. They showed that the decimal value (D-value) varies from several tens of seconds to several minutes depending on the type of bacteria and medium supporting the cells. Laroussi et al. used the RBD to study the effect of cold plasma on the heterotrophic pathways and morphology of bacteria[34]. As representative bacteria they used Escherichia. coli (Gram-negative) and Bacillus subtilis (Gram-positive). They addressed these questions by using sole carbon substrate utilization (SCSU) and electron microscopy. They reported that sub-lethally cold plasma can affect cells’ enzyme functions and for longer exposure to plasma E. coli underwent lysis. Although inactivated, B. subtilis cells were not necessarily lysed[34]. Laroussi et al. also reported that the lysing of cells could be explained by charge accumulation on the cell’s outer membrane[35]. This causes the creation of an outward electrostatic tension that stretches the membrane. The magnitude of this force is a function of the surface potential and is greater for a smaller radius of curvature. So in location where this radius is very small the electrostatic force can overcome the tensile strength of the membrane and therefore causes local disruption[35]. They argued that the outer membrane of E. coli exhibits an irregular/rough surface with small “bumps/pimples” with very small radii of curvature. This, they argue, why it is easier to lyse Gram-negative bacteria[35]. It is important to note here that the lysing of cells could happen because of other causes such as the oxidation and/or peroxidation reactions in the cell membrane. In addition electroporation that is caused by the presence of electric fields can lead to the opening of pores in the cell membrane, some of which may be irreversible.
Thyigarajan et al. used the RBD in helium and air to inactivate E. coli. They reported total killing of the bacterial population in 180 s (but they did not specify the original concentration)[36]. They detected high concentrations of ozone and traces of NO2. They attributed these species to the efficient inactivation they observed[36].
Uhm et al. reported on a sterilization chamber that uses several layers of RBDs to generate large volume plasmas (40 L)[37]. They used this chamber to sterilize medical tools wrapped in hospital cloths, to sterilize manufactured drugs in typical packaging materials, and to sterilize biologically contaminated article[37]. As operating gas they used oxygen and therefore created mostly ozone to interact with items to be sterilized. It took an applied power of 60 W and residence time of 5 h to accomplish sterilization[37]. They also used an ozone destruction device to eliminate the ozone after usage.
Thyiagarajan et al. used an RBD specifically designed to mostly produce RNS to study their effect on human myeloid leukemia cells[38]. The effect of variable treatments of plasma-generated RNS was tested in THP-1 cells (human monocytic leukemia cell line), a model for hematological malignancy. These investigators used erythrosine-B staining to evaluate the number of viable cells. Apoptosis and necrosis were assessed by endonuclease cleavage observed by agarose gel electrophoresis. Cells detection was done with propidium iodide (exclusionary dye) and fluorescently labeled annexin-V by flow cytometry and fluorescent microscopy[38]. They reported that treatment times less than 45 s induced apoptotic cell death while for times equal or greater than 50 s necrosis was observed. They suggested that these effects were due to the RNS generated by the RBD, however, they did not specify the specific nitrogen species.