Plasma Medicine

Cold atmospheric-pressure plasma show promising antimicrobial effects, however the detailed biochemical mechanism of the bacterial inactivation is still unknown. We investigated, for the first time, plasma-treated Gram-positive Bacillus subtilis and Gram-negative Escherichia coli bacteria with Raman and infrared microspectroscopy. A dielectric barrier discharge was used as a plasma source. We were able to detect several plasma-induced chemical modifications, which suggest a pronounced oxidative effect on the cell envelope, cellular proteins and nucleotides as well as a generation of organic nitrates in the treated bacteria. Vibrational microspectroscopy is used as a comprehensive and a powerful tool for the analysis of plasma interactions with whole organisms such as bacteria. Analysis of reaction kinetics of chemical modifications allow a time-dependent insight into the plasma-mediated impact. Investigating possible synergistic effects between the plasma-produced components, our observations strongly indicate that the detected plasma-mediated chemical alterations can be mainly explained by the particle effect of the generated reactive species. By changing the polarity of the applied voltage pulse, and hence the propagation mechanisms of streamers, no significant effect on the spectral results could be detected. This method allows the analysis of the individual impact of each plasma constituent for particular chemical modifications. Our approach shows great potential to contribute to a better understanding of plasma-cell interactions.

American Foulbrood is a severe, notifiable disease of the honey bee. It is caused by infection of bee larvae with spores of the gram-positive bacterium Paenibacillus larvae. Spores of this organism are found in high numbers in an infected hive and are highly resistant to physical and chemical inactivation methods. The procedures to rehabilitate affected apiaries often result in the destruction of beehive material. In this study we assess the suitability of a double inductively coupled low pressure plasma as a non-destructive, yet effective alternative inactivation method for bacterial spores of the model organism Bacillus subtilis on beehive material. Plasma treatment was able to effectively remove spores from wax, which, under protocols currently established in veterinary practice, normally is destroyed by ignition or autoclaved for sterilization. Spores were removed from wooden surfaces with efficacies significantly higher than methods currently used in veterinary practice, such as scorching by flame treatment. In addition, we were able to non-destructively remove spores from the highly delicate honeycomb wax structures, potentially making treatment of beehive material with double inductively coupled low pressure plasma part of a fast and reliable method to rehabilitate infected bee colonies with the potential to re-use honeycombs.

Our dielectric barrier discharge (DBD) plasma source for bio-medical application comprises a copper electrode covered with ceramic. Objects of high capacitance such as the human body can be used as the opposite electrode. In this study, the DBD source is operated in single-filamentary mode using an aluminium spike as the opposite electrode, to imitate the conditions when the discharge is ignited on a raised point, such as hair, during therapeutic use on the human body. The single-filamentary discharge thus obtained is characterized using optical emission spectroscopy, numerical simulation, voltage–current measurements and microphotography. For characterization of the discharge, averaged plasma parameters such as electron distribution function and electron density are determined. Fluxes of nitric oxide (NO), ozone (O₃) and photons reaching the treated surface are simulated. The calculated fluxes are finally compared with corresponding fluxes used in different bio-medical applications.

We report for the first time the deposition of fluorocarbon thin films on outer and inner surfaces of millimetric sized diameter stainless steel mini-tubes by radiofrequency pulsed plasma polymerization for coronary stent applications. The deposition was performed under a glow discharge with a mixture of hexafluorethylene (C₂F₆) and hydrogen in a post-discharge configuration with substrates kept at floating potential or continuously biased with a negative voltage of up to 1000 V. Film composition, structure, uniformity and covering efficiency on outer and inner surfaces along the mini-tubes were characterized by scanning electron microscopy, Fourier-transformed infrared spectroscopy, x-ray photoelectron spectroscopy and atomic force microscopy. At floating potential, a coating of fluorocarbon (CF_x) was deposited varying in chemical composition and thickness along the mini-tube axis. The application of a −400 V bias voltage led to outer surfaces with a fluorocarbon coating uniform in thickness and homogeneous in composition, along the full length of the mini-tube (10 mm). Despite the application of a negative bias, the covering efficiency for the inner surface was lower compared with the outer surface, with fluorocarbon films homogeneous in both composition and thickness until half length of the mini-tube (5 mm) but thickness decreasing afterwards. Strategies for amelioration of the latter limitation are proposed.

Antimicrobial effectiveness of a nanosecond-pulsed dielectric barrier discharge (DBD) was investigated and compared with that of a microsecond-pulsed DBD. Experiments were conducted on the Escherichia coli bacteria covering a topographically non-uniform agar surface acting as one of the DBD electrodes. They reveal that the nanosecond-pulsed DBD can inactivate bacteria in recessed areas whereas the microsecond-pulsed and conventional DBDs fail to do so. Charged species (electrons and ions) appear to play the major role in the bacteria inactivation with the nanosecond-pulsed DBD. Moreover, the nanosecond-pulsed DBD kills bacteria significantly faster than its microsecond-pulsed counterpart.

A low-pressure inductively coupled plasma discharge sustained in an argon–oxygen–nitrogen ternary mixture is studied in order to evaluate its properties in terms of sterilization and decontamination of surfaces of medical instruments. It is demonstrated by direct comparison with discharges operated in oxygen–nitrogen and oxygen–argon mixtures that application of an Ar/O₂/N₂ mixture offers the possibility to combine advantageous properties of the binary mixtures, namely, the capability of an O₂/N₂ plasma to emit intense UV radiation needed for effective inactivation of bacterial spores together with high removal rates of biological substances from Ar/O₂ discharge. Moreover, optimal conditions for both effects are obtained at a similar ternary discharge mixture composition, which is of much interest for real applications, since it offers a highly effective process desired for the safety of medical instruments.

The dielectric barrier discharge (DBD) plasma source for biomedical application is characterized using optical emission spectroscopy, plasma-chemical simulation and voltage–current measurements. This plasma source possesses only one electrode covered by ceramic. Human body or some other object with enough high electric capacitance or connected to ground can serve as the opposite electrode. DBD consists of a number of microdischarge channels distributed in the gas gap between the electrodes and on the surface of the dielectric. To characterize the plasma conditions in the DBD source, an aluminium plate is used as an opposite electrode. Electric parameters, the diameter of microdischarge channel and plasma parameters (electron distribution function and electron density) are determined. The gas temperature is measured in the microdischarge channel and calculated in afterglow phase. The heating of the opposite electrode is studied using probe measurement. The gas and plasma parameters in the microdischarge channel are studied at varied distances between electrodes. According to an energy balance study, the input microdischarge electric energy dissipates mainly in heating of electrodes (about 90%) and partially (about 10%) in the production of chemical active species (atoms and metastable molecules).

Ambient air plasmas have been known to kill cancer cells. To enhance selectivity we have used antibody-conjugated nanoparticles. We achieved five times enhancement of melanoma cell death over the case of the plasma alone by using an air plasma with gold nanoparticles bound to anti-FAK antibodies. Our results show that this new interdisciplinary technique has enormous potential for use as a complement to conventional therapies.

Non-equilibrium low pressure-plasma discharges are extensively studied for their high potential in the field of sterilization and decontamination of medical devices. This increased interest in plasma discharges arises from, among other reasons, their capability not only to inactivate bacterial spores but also to eliminate, destroy or remove pathogenic biomolecules and thus to provide a one-step process assuring safety of treated instruments. However, recent studies have shown that optimal conditions leading to inactivation of spores and physical removal of pathogens differ significantly—the efficiency of spores sterilization is above all dependent on the UV radiation intensity, whereas high etching rates are connected with the presence of the etching agent, typically atomic oxygen. The aim of this contribution is to discuss and demonstrate the feasibility of Ar/N₂/O₂ low-pressure inductively coupled plasma discharges as an option to provide intense UV radiation while maintaining the high etching rates of biomolecules.

This paper introduces a new type of high-frequency (HF) sustained discharge where the HF field applicator is a planar transmission line that allows us to fill with plasma a long chamber of rectangular cross-section (typically 1 m × 15 cm × 5 cm). Peculiar interesting features of this plasma source are a low gas temperature (typically below 40 °C in the 1 Torr range in argon), broadband impedance matching with no need for retuning, stability and reproducibility of the discharge (non-resonant behaviour). This type of plasma source could be useful for web processing; nonetheless, it is applied here to plasma sterilization, taking advantage of its low gas temperature to inactivate microorganisms on polymer-made medical devices to avoid damaging them. The predominant biocide species are the UV photons emitted by the discharge whereas most plasma sterilization techniques call for reactive species such as O atoms and OH molecules, which induce significant erosion damage on polymers. Polystyrene microspheres are actually observed to be erosion-free under the current plasma sterilization conditions (scanning electron micrographs have been examined). Moreover, inactivation is quite fast: 10⁶ B. atrophaeus spores deposited on a Petri dish are inactivated in less than 1 min. Correlation of the UV radiation with the spore inactivation rate is examined by (i) considering the emitted light intensity integrated over the 112–180 nm vacuum UV (VUV) range with a photomultiplier; (ii) looking with an optical spectrometer at the emission spectrum over the 200–400 nm UV range; (iii) using absorption spectroscopy to determine the role of the VUV argon resonant lines (105 and 107 nm) on spore inactivation. It is found that the test-reference spores are mainly inactivated by VUV photons (112–180 nm) that are primarily emitted by impurities present in the argon plasma.

The inactivation of spores of Bacillus atrophaeus and of Aspergillus niger using beams of argon ions, of oxygen molecules and of oxygen atoms is studied. Thereby, the conditions occurring in oxygen containing low pressure plasmas are mimicked and fundamental inactivation mechanisms can be revealed. It is shown that the impact of O atoms has no effect on the viability of the spores and that no etching of the spore coat occurs up to an O atom fluence of 3.5 × 10¹⁹ cm⁻². The impact of argon ions with an energy of 200 eV does not cause significant erosion for fluences up to 1.15 × 10¹⁸ cm⁻². However, the combined impact of argon ions and oxygen molecules or atoms causes significant etching of the spores and significant inactivation. This is explained by the process of chemical sputtering, where an ion-induced defect at the surface of the spore reacts with either the incident bi-radical O₂ or with an incident O atom. This leads to the formation of CO, CO₂ and H₂O and thus to erosion.

Ar + NO microwave discharges are used for sterilization and the results are compared with additional experiments with Ar, O₂ and N₂–O₂ plasma mixtures. The NO^* species produced in the Ar–NO mixtures remain up to long distances from the source, thus improving the sterilization efficiency of the process. E. coli individuals exposed to the Ar + NO plasma undergo morphological damage and cell lysis. Combined effects of etching (by O^* and Ar^* species) and UV radiation (from deactivation of NO^* species) are responsible for the higher activity found for this plasma mixture.

Surgical instruments are intended to come into direct contact with the patients' tissues and thus interact with their first immune defence system. Therefore they have to be cleaned, sterilized and decontaminated, in order to prevent any kind of infections and inflammations or to exclude the possibility of transmission of diseases. From this perspective, the removal of protein residues from their surfaces constitutes new challenges, since certain proteins exhibit high resistance to commonly used sterilization and decontamination techniques and hence are difficult to remove without inducing major damages to the object treated. Therefore new approaches must be developed for that purpose and the application of non-equilibrium plasma discharges represents an interesting option. The possibility to effectively remove model proteins (bovine serum albumin, lysozyme and ubiquitin) from surfaces of different materials (Si wafer, glass, polystyrene and gold) by means of inductively coupled plasma discharges sustained in different argon containing mixtures is demonstrated and discussed in this paper.

Metallic intravascular stents are medical devices (316L stainless steel) used to support the narrowed lumen of atherosclerotic stenosed arteries. Despite the success of bare metal stents, restenosis remains the main complication after 3–6 months of implantation. To reduce the restenosis rate of bare metal stents, stent coating is an interesting alternative. Firstly, it allows the modification of the surface properties, which is in contact with the biological environment. Secondly, the coating could eventually act as a carrier for drug immobilization and release. Moreover, the in vivo stent implantation requires in situ stent expansion. This mandatory step generates local plastic deformation of up to 25% and may cause coating failures such as cracking and delamination. Fluorocarbon films were selected in this study as a potential stent coating, mainly due to their chemical inertness, high hydrophobicity, protein retention capabilities and thromboresistance properties. The aim of this study was to investigate the adhesion properties of fluorocarbon films of three different thicknesses deposited by plasma polymerization in C₂F₆/H₂ on 316L stainless steel substrates. A previously developed small punch test was used to deform the coated samples. According to atomic force microscopy, field emission scanning electron microscopy and x-ray photoelectron spectroscopy characterizations, among the coatings with different thicknesses studied, only those with a thickness of 36 nm exhibited the required cohesion and interfacial adhesion to resist the stent expansion without cracking or delaminating. Otherwise, cracks were detected in the coatings having thicknesses equal or superior to 100 nm, indicating a lack of cohesion.

Currently, there is a strong tendency to replace rigid electronic assemblies by mechanically flexible and stretchable equivalents. This emerging technology can be applied for biomedical electronics, such as implantable devices and electronics on skin. In the first step of the production process of stretchable electronics, electronic interconnections and components are encapsulated into a thin layer of polydimethylsiloxane (PDMS). Afterwards, the electronic structures are completely embedded by placing another PDMS layer on top. It is very important that the metals inside the electronic circuit do not leak out in order to obtain a highly biocompatible system. Therefore, an excellent adhesion between the 2 PDMS layers is of great importance. However, PDMS has a very low surface energy, resulting in poor adhesion properties. Therefore, in this paper, PDMS films are plasma treated with a dielectric barrier discharge (DBD) operating in air at medium pressure (5.0 kPa). Contact angle and XPS measurements reveal that plasma treatment increases the hydrophilicity of the PDMS films due to the incorporation of silanol groups at the expense of methyl groups. T-peel tests show that plasma treatment rapidly imparts adhesion enhancement, but only when both PDMS layers are plasma treated. Results also reveal that it is very important to bond the plasma-treated PDMS films immediately after treatment. In this case, an excellent adhesion is maintained several days after treatment. The ageing behaviour of the plasma-treated PDMS films is also studied in detail: contact angle measurements show that the contact angle increases during storage in air and angle-resolved XPS reveals that this hydrophobic recovery is due to the migration of low molar mass PDMS species to the surface.

The identification of sterilization agents is mandatory to achieve sterilization mechanisms in low-pressure discharges. A detailed account of each agent is required for improvements, development and establishment of plasma sterilization as an alternative to traditional sterilization processes. Sterilization agents are VUV and UV radiation, photodesorption producing volatile species and etching of spore coat and membrane. This work focuses on VUV and UV radiation as a sterilization agent of Bacillus atrophaeus spores. Four wavelength ranges are distinguished: the emission spectra above 300 nm, above 235 nm, above 112 nm and a full emission spectrum including active species. The range from 235 up to 300 nm without active species is identified to be the most capable for sterilizing Bacillus atrophaeus spores.

A double inductively coupled low pressure plasma for sterilization of bio-medical materials is introduced. It is developed for homogeneous treatment of three-dimensional objects. The short treatment times and low temperatures allow the sterilization of heat sensitive materials like ultra-high-molecular-weight-polyethylene or polyvinyl chloride. Using a non-toxic atmosphere reduces the total process time in comparision with common methods. Langmuir probe measurements are presented to show the difference between ICP- and CCP-mode discharges, the spatial homogeneity and the influence on the sterilization efficiency. To know more about the sterilization mechanisms optical emission is measured and correlated with sterilization results.

The inactivation of bacteria by plasma discharges offers the unique benefits of short treatment times, minimal damage to the objects being sterilized and minimal use of hazardous chemicals. Plasmas produce reactive fluxes of ions, atoms and UV photons from any given precursor gas and are expected to be a viable method for such sterilization applications. The plasma based inactivation of harmful biological systems is, however, not yet widely used, because any validation is hampered by the limited knowledge about the interaction mechanisms at the interface between a plasma and a biological system. By using quantified beams of hydrogen atoms, argon ions and UV photons, the treatment of bacteria in a typical argon–hydrogen plasma is mimicked in a very controlled manner. As an example the inactivation of endospores of Bacillus atrophaeus is studied. It is shown that the impact of H atoms alone causes no inactivation of bacteria. Instead, the simultaneous impact of atoms and low energy ions causes a perforation of the endosporic shell. The same process occurs during plasma treatment and explains the efficient inactivation of bacteria.

In this work a low-cost parallel technique for creating chemical nano-patterned surfaces using nano-spheres as masks is presented. This technique, called nano-sphere lithography, makes use of different steps of plasma etching and deposition processes, for the creation of polymeric nano-structures of different chemical functionalities with relevant applications to bio-interfaces. In this study, the attention is focused on the plasma processing aspects for the etching of the polymeric masks (colloidal masks) in order to control the shape and the size of the etched nano-structures. The bio-functionality of the nano-patterned surfaces has been proved with a selective immobilization of proteins on the bioactive spots.

A novel atmospheric pressure plasma device releasing atomic hydrogen has been developed. This device has specific properties such as (1) deactivation of airborne microbial-contaminants, (2) neutralization of indoor OH radicals and (3) being harmless to the human body. It consists of a ceramic plate as a positive ion generation electrode and a needle-shaped electrode as an electron emission electrode. Release of atomic hydrogen from the device has been investigated by the spectroscopic method. Optical emission of atomic hydrogen probably due to recombination of positive ions, H⁺(H₂O)n, generated from the ceramic plate electrode and electrons emitted from the needle-shaped electrode have been clearly observed in the He gas (including water vapour) environment. The efficacy of the device to reduce airborne concentrations of influenza virus, bacteria, mould fungi and allergens has been evaluated. 99.6% of airborne influenza virus has been deactivated with the operation of the device compared with the control test in a 1 m³ chamber after 60 min. The neutralization of the OH radical has been investigated by spectroscopic and biological methods. A remarkable reduction of the OH radical in the air by operation of the device has been observed by laser-induced fluorescence spectroscopy. The cell protection effects of the device against OH radicals in the air have been observed. Furthermore, the side effects have been checked by animal experiments. The harmlessness of the device has been confirmed.

A three-dimensional hydrodynamic model is developed to simulate a post-discharge reactor placed downstream from a flowing microwave discharge in N₂–O₂ used for plasma sterilization. The temperature distribution and the density distributions of NO(B ²Π) molecules and O(³P) atoms, which are known to play a central role in the sterilization process, are obtained in the reactor in the case of discharges at 915 and 2450 MHz, pressure range 1–8 Torr and N₂–xO₂ mixture composition, with x = 0.2–2%. Excluding the flow direction, sufficiently low temperatures ideal for sterilization have been found in most parts of the reactor. The highest NO(B) and O(³P) concentrations at the reactor entrance are achieved at the highest pressure values investigated here. However, these larger densities rapidly decrease within a few centimetres below the values obtained at lower pressure. On the contrary, at low pressure the density distributions of NO(B) and O(³P) are quasi-homogeneous in most of the horizontal planes. At 8 Torr the densities increase orders of magnitude in the reactor as the gas flow increases from 1 × 10³ to 4 × 10³ sccm, while at 2 Torr this increase does not reach even one order of magnitude. In agreement with the experiment, the densities of NO(B) and O(³P) have been found to increase at 2 Torr as the O₂ percentage increases in the discharge gas mixture, whereas at 8 Torr the density of NO(B) decreases with O₂ percentage and the O(³P) density presents only minor changes.

We report results from a two-dimensional, axisymmetric numerical simulation of the plasma needle, powered at 13.56 MHz. The atmospheric pressure discharge is simulated in helium with a small amount of nitrogen. The needle has a point-to-plane geometry with a radius of 30 µm at the tip and an inter-electrode gap of 1 mm. We employ the one-moment fluid model with local field approximation. The coupled continuity equations for electrons, ions and metastables are solved with Poisson's equation using the finite element method with an unstructured grid. The discharge voltage–power characteristic demonstrates a region in which multiple solutions exist for a given applied RF voltage. This mode transition in the plasma needle resembles an α–γ transition from a lower plasma density regime with a relatively thick sheath at the needle tip to a higher plasma density regime with a relatively thin sheath at the needle tip.

Repetitive plasma discharges developed in saline solutions have been investigated using fast, intensified charge coupled detector imaging techniques. The images show that synchronously pulsed multielectrode configurations tend to develop intense, transient plasma regions somewhat randomly in both space and time on short (10 µs) time scales, even though they appear to be stationary on longer (tens of milliseconds) time scales. Evidence for the production of both strongly ionized and weakly ionized plasmas is also presented.

Plasma polymer surface modification is widely used in the biomedical field to tailor the surface properties of materials to improve their biocompatibility. Most of these treatments are performed using low pressure plasma systems but recently, filamentary dielectric barrier discharge (FDBD) and atmospheric pressure glow discharge (APGD) have appeared as interesting alternatives. The aim of this paper is to evaluate the potential of surface modifications realized with FDBD and APGD in different atmospheres (N₂+ H₂ and N₂+ NH₃ mixtures) on poly(tetrafluoroethylene) to determine the relative influence of both the discharge regime and the gas nature on the surface transformations. From XPS analysis, it is shown that the discharge regime can have a significant effect on the surface transformation; FDBDs operating in H₂/N₂ lead to a high concentration of amino-groups with high specificity but also important damaging on the surface. Glow discharges in both H₂/N₂ and NH₃/N₂ lead to lower concentrations of amino-groups with lower specificity but lower surface damaging. Therefore, this simple surface treatment seems to be an effective, low cost method for the production of uniform surface modification with amino-groups that can subsequently be used to graft various chemical functionalities used for biomaterial compatibility.

The role of gas flow and transport mechanisms are studied for a small low-power impinging jet of weakly-ionized helium at atmospheric pressure. This plasma needle produces a non-thermal glow discharge plasma that kills bacteria. A culture of Streptococcus mutans (S. mutans) was plated onto the surface of agar, and spots on this surface were then treated with plasma. Afterwards, the sample was incubated and then imaged. These images, which serve as a biological diagnostic for characterizing the plasma, show a distinctive spatial pattern for killing that depends on the gas flow rate. As the flow is increased, the killing pattern varies from a solid circle to a ring. Images of the glow reveal that the spatial distribution of energetic electrons corresponds to the observed killing pattern. This suggests that a bactericidal species is generated in the gas phase by energetic electrons less than a millimetre from the sample surface. Mixing of air into the helium plasma is required to generate the observed O and OH radicals in the flowing plasma. Hydrodynamic processes involved in this mixing are buoyancy, diffusion and turbulence.

A critical approach to plasma sterilization is presented with the aim of sterilizing biocompatible materials such as TiO₂ and polymer implants. Oxygen plasma was applied to sterilize glass and aluminium samples containing Bacillus subtilis spores. Sterilization was performed with a low pressure weakly ionized oxygen plasma created with a RF generator with an output power of 300 W and frequency 27.12 MHz. The density of charged particles, density of neutral oxygen atoms and the electron temperature were about 1 × 10¹⁶ m⁻³, 1.5 × 10²² m⁻³ and 5 eV, respectively. The sterilization effects were observed by SEM and by bacterial cultivation. It was found that the surface recombination of O-atoms plays an important role, since it causes temperature changes in the substrate. The sterilization efficiency increased with increasing plasma exposure time. The results showed that the sterilization efficiency is not necessarily just the effect of oxygen plasma radical interactions, but also of the sample heating due to radical interaction with the substrate. Plasma sterilization should be done differently according to the substrate material used for sterilization.

This paper comprises two main parts: a review of the literature on atmospheric-pressure discharges used for micro-organism inactivation, focused on the inactivation mechanisms, and a presentation of our research results showing, in particular, that UV photons can be the dominant species in the inactivation process.

The possibility of achieving spore inactivation through UV radiation using an atmospheric-pressure discharge or its flowing afterglow is the object of a continuing controversy. In fact, the review of the literature that we present shows that a majority of researchers have come to the conclusion that, at atmospheric pressure, chemically reactive species such as free radicals, metastable atoms and molecules always control the inactivation process, while UV photons play only a minor role or no role at all. In contrast, only a few articles suggest or claim that UV photons coming from atmospheric-pressure discharges can, in some cases, inactivate micro-organisms, but the experimental data presented and the supporting arguments brought forward in that respect are relatively incomplete.

Using a dielectric-barrier discharge operated at atmospheric pressure in an N₂–N₂O mixture, we present, for the first time, experiments where micro-organisms are subjected to plasma conditions such that, on the one hand, UV radiation is strong or, on the other hand, there is no UV radiation, the two different situations being obtained with the same experimental arrangement, including the same gas mixture, N₂–N₂O. To achieve maximum UV radiation, the concentration of the oxidant molecule (N₂O) added to N₂ needs to be tuned carefully, resulting then in the fastest inactivation rate. The concentration range of the oxidant molecule in the mixture for which the UV intensity is significant is extremely narrow, a fact that possibly explains why such a mode of plasma sterilization was not readily observed. The survival curves obtained under dominant UV radiation conditions are, as we show, akin to those recorded at reduced pressure. Relatively fast spore inactivation can also be obtained under no UV radiation as a result of radicals diffusing deeply inside the spores, leading to oxidative lethal damage.

A miniature atmospheric pressure glow discharge plasma torch was used to detach cells from a polystyrene Petri dish. The detached cells were successfully transplanted to a second dish and a proliferation assay showed the transplanted cells continued to grow. Propidium iodide diffused into the cells, suggesting that the cell membrane had been permeabilized, yet the cells remained viable 24 h after treatment. In separate experiments, hydrophobic, bacteriological grade polystyrene Petri dishes were functionalized. The plasma treatment reduced the contact angle from 93° to 35°, and promoted cell adhesion. Two different torch nozzles, 500 µm and 150 µm in internal diameter, were used in the surface functionalization experiments. The width of the tracks functionalized by the torch, as visualized by cell adhesion, was approximately twice the inside diameter of the nozzle. These results indicate that the miniature plasma torch could be used in biological micropatterning, as it does not use chemicals like the present photolithographic techniques. Due to its small size and manouvrability, the torch also has the ability to pattern complex 3D surfaces.

Argon plasma coagulation is an application of gas discharges in argon in electrosurgery, which is increasingly being used especially in endoscopy. This review describes the underlying physics and technology, gives some application examples, and discusses new developments.

The pulsed electric field (PEF) treatment of liquid and pumpable products contaminated with microorganisms has attracted significant interest from the pulsed power and bioscience research communities particularly because the inactivation mechanism is non-thermal, thereby allowing retention of the original nutritional and flavour characteristics of the product. Although the biological effects of PEF have been studied for several decades, the physical mechanisms of the interaction of the fields with microorganisms is still not fully understood. The present work is a study of the dynamics of the electrical field both in a PEF treatment chamber with dielectric barriers and in the plasma (cell) membrane of a microbial cell. It is shown that the transient process can be divided into three physical phases, and models for these phases are proposed and briefly discussed. The complete dynamics of the time development of the electric field in a spherical dielectric shell representing the cellular membrane is then obtained using an analytical solution of the Ohmic conduction problem. It was found that the field in the membrane reaches a maximum value that could be two orders of magnitude higher than the original Laplacian electrical field in the chamber, and this value was attained in a time comparable to the field relaxation time in the chamber. Thus, the optimal duration of the field during PEF treatment should be equal to such a time.