Helena Tresp

Quantitative detection of plasma-generated radicals in liquids by electron paramagnetic resonance spectroscopy

In this paper the qualitative and quantitative detection of oxygen radicals in liquids after plasma treatment with an atmospheric pressure argon plasma jet by electron paramagnetic resonance spectroscopy is investigated. Absolute values for ?OH and radical concentration and their net production rate in plasma-treated liquids are determined without the use of additional scavenging chemicals such as superoxide dismutase (SOD) or mannitol (D-MAN). The main oxygen-centred radical generation in PBS was found to originate from the superoxide radical. It is shown that hidden parameters such as the manufacturer of chemical components could have a big influence on the comparability and reproducibility of the results. Finally, the effect of a shielding gas device for the investigated plasma jet with a shielding gas composition of varying oxygen-to-nitrogen ratio on radical generation after plasma treatment of phosphate-buffered saline solution was investigated.

Feed gas humidity: a vital parameter affecting a cold atmospheric-pressure plasma jet and plasma-treated human skin cells

In this study, the effect of feed gas humidity on the reactive component generation of an atmospheric-pressure argon plasma jet and its effect on human skin cells are investigated. Feed gas humidity is identified as one key parameter that strongly influences stability and reproducibility of plasma medical studies. The plasma jet is investigated by absorption spectroscopy in the ultraviolet and infrared spectral region for its ozone production depending on the humidity concentration in the feed gas. By optical emission spectroscopy the dependence of present excited plasma species such as hydroxyl radicals, molecular nitrogen, argon and atomic oxygen on the feed gas humidity is investigated. As an interface layer between the plasma jet effluent and the biological cell, a buffer solution is treated and the hydrogen peroxide (H2O2) production is studied with two independent colorimetric assays as a function of humidity admixture to the feed gas. Ultimately, the effect of varying feed gas humidity on the cell viability of indirect plasma treated adherent HaCAT cells is investigated. The highest viability is found for the driest feed gas condition. Furthermore, this work shows answers for the relevance of unwanted—or intended—feed gas humidity in plasma medical experiments and their comparatively large relevance with respect to ambient humidity. The findings will lead to more reproducible experiments in the field of plasma medicine.

Atmospheric pressure plasma: a high-performance tool for the efficient removal of biofilms.

Introduction The medical use of non-thermal physical plasmas is intensively investigated for sterilization and surface modification of biomedical materials. A further promising application is the removal or etching of organic substances, e.g., biofilms, from surfaces, because remnants of biofilms after conventional cleaning procedures are capable to entertain inflammatory processes in the adjacent tissues. In general, contamination of surfaces by micro-organisms is a major source of problems in health care. Especially biofilms are the most common type of microbial growth in the human body and therefore, the complete removal of pathogens is mandatory for the prevention of inflammatory infiltrate. Physical plasmas offer a huge potential to inactivate micro-organisms and to remove organic materials through plasma-generated highly reactive agents. Method In this study a Candida albicans biofilm, formed on polystyrene (PS) wafers, as a prototypic biofilm was used to verify the etching capability of the atmospheric pressure plasma jet operating with two different process gases (argon and argon/oxygen mixture). The capability of plasma-assisted biofilm removal was assessed by microscopic imaging. Results The Candida albicans biofilm, with a thickness of 10 to 20 µm, was removed within 300 s plasma treatment when oxygen was added to the argon gas discharge, whereas argon plasma alone was practically not sufficient in biofilm removal. The impact of plasma etching on biofilms is localized due to the limited presence of reactive plasma species validated by optical emission spectroscopy.

Tracking plasma generated H2O2 from gas into liquid phase and revealing its dominant impact on human skin cells

The pathway of the biologically active molecule hydrogen peroxide (H2O2) from the plasma generation in the gas phase by an atmospheric pressure argon plasma jet, to its transition into the liquid phase and finally to its inhibiting effect on human skin cells is investigated for different feed gas humidity settings. Gas phase diagnostics like Fourier transformed infrared spectroscopy and laser induced fluorescence spectroscopy on hydroxyl radicals (OH) are combined with liquid analytics such as chemical assays and electron paramagnetic resonance spectroscopy. Furthermore, the viability of human skin cells is measured by Alamar Blue® assay. By comparing the gas phase results with chemical simulations in the far field, H2O2 generation and destruction processes are clearly identified. The net production rate of H2O2 in the gas phase is almost identical to the H2O2 net production rate in the liquid phase. Moreover, by mimicking the H2O2 generation of the plasma jet with the help of an H2O2 bubbler it is concluded that the solubility of gas phase H2O2 plays a major role in generating hydrogen peroxide in the liquid. Furthermore, it is shown that H2O2 concentration correlates remarkably well with the cell viability. Other species in the liquid like OH or superoxide anion radical do not vary significantly with feed gas humidity.

From RONS to ROS: Tailoring Plasma Jet Treatment of Skin Cells

Finding a solution for air species contamination of atmospheric pressure plasmas in plasma medical treatment is a major task for the new field of plasma medicine. Several approaches use complex climate chambers to control the surrounding atmosphere. In this paper, ambient species are excluded in plasma-human-skin-cell treatment by ensheathing the plasma jet effluent with a shielding gas. Not only does this gas curtain protect the plasma jet effluent from inflow of air species but it also, more importantly, allows controlling the effluent reactive species composition by adjusting the mixture of the shielding gas. In the present investigations, the mixture of nitrogen to oxygen within the gas curtain around an argon atmospheric pressure plasma jet (kinpen) is varied. The resulting reactive plasma components produced in the jet effluent are thus either oxygen or nitrogen dominated. With this gas curtain, the effect of reactive oxygen species (ROS) and reactive nitrogen species (RNS) on the cell viability of indirectly plasma-treated HaCaT skin cells is studied. This human keratinocyte cell line is an established standard for a skin model system. The cell viability is determined by a fluorometric assay, where metabolically active cells transform nonfluorescent resazurin to the highly fluorescent resorufin. Plasma jet and gas curtain are characterized by numerical flow simulation as well as by optical emission spectroscopy. The generation of nitrite within the used standard cell culture medium serves as a measure for generated RNS. Measurements with the leukodye dichlorodihydrofluorescein diacetate show that, despite a variation of the shielding gas mixture, the total amount of generated reactive oxygen plus nitrogen species is constant. It is shown that a plasma dominated by RNS disrupts cellular growth less than a ROS-dominated plasma.

Controlling the Ambient Air Affected Reactive Species Composition in the Effluent of an Argon Plasma Jet

The influence of ambient air species is an ever-present problem for atmospheric pressure plasma jet applications. In particular, applications where the plasma-induced effects are extremely sensitive to specific types of ambient species (oxygen, nitrogen, humidity) - as, for example, in plasma medicine - require concepts to exclude or to control ambient species flux into the jet effluent that go beyond an environmental control via process chambers or even vacuum systems. In this paper, we demonstrate how to eliminate ambient species influence on effluent chemistry by ensheathing the effluent. With a designed shielding gas composition, we control the species flowing into the jet effluent and thus control the effluent chemistry. The proposed approach can be applied to the majority of possible jet plasma sources. Flow simulations as well as VUV-absorption spectroscopy measurements prove the gas curtain to be effective in shielding the jet gas from ambient species and show that a control of reactive species within the jet effluent is possible. On the example of plasma treatment of a NaCl solution, we demonstrate that, by adjusting the shielding gas composition, the generation of nitrite and nitrate in the solution can be finely controlled.

Non-thermal plasma treatment induces MAPK signaling in human monocytes

Abstract The application of non-thermal atmospheric pressure plasma raises a hope for the new wound healing strategies. Next to its antibacterial effect it is known to stimulate skin cells. However, monocytes are also needed for the complex process of a wound healing. This study investigates the impact of plasma on the intracellular signaling events in the primary human monocytes. The proliferative MEK-ERK (MAPK/ERK kinase-extracellular signal-regulated kinase) pathway was activated by short plasma treatment times. In contrast, an induction of the apoptotic JNK (c-Jun N-terminal kinase) cascade as well as activation of caspase 3 were observed after long plasma exposure. These findings indicate that monocytes can be differentially stimulated by plasma treatment and may contribute to the proper wound recovery. Graphical Abstract

Feed gas humidity versus ambient humidity — What matters more in plasma medicine and what makes cells care?

Summary form only given. Humidity plays an important role in plasma chemistry and influences the production of a variety of reactive species like OH, H2O2 or O3. This is especially true in the fast growing field of plasma medicine where patients are supposed to be treated under ambient conditions with changing humidity concentrations. Also when humidity is present in the feed gas of the plasma source - unwanted or intended - a change in the plasma produced active species is obtained. In this paper the influence of ambient humidity and feed gas humidity on the effluent of an atmospheric pressure argon plasma jet is investigated by means of optical emission spectroscopy, Fourier transformed infrared spectroscopy inside a white cell with an effective absorption length of 19.2 m, as well as absorption spectroscopy in the UV and IR spectral range. With these techniques gas phase production rates of H2O2, O3 and NO2 as well as spatial distributions of excited plasma species like Ar, O, N2 and OH are determined in dependence of the humidity concentration. On basis of the presented results it is shown that feed gas humidity is more relevant to consider than ambient humidity. However, when constant feed gas humidity concentrations are experimentally provided changes in ambient humidity become relevant again. In order to give an impression of how crucial feed gas humidity influence is on indirect plasma treated human skin cells results of a viability assay are presented1. These results are correlated to the liquid phase production of H2O2 molecules as well as O2and OH radicals in liquid cell growth medium. Applied measurement techniques are colorimetric assays for determination of the H2O2 density and electron spin resonance spectroscopy for O2and OH radical densities. A remarkable correlation of the cell viability with H2O2 concentration was found whereas O2 and OH do not seem to have a direct effect.