SYSTEM AND PLASMA FOR TREATING AND/OR PREVENTING A VIRAL, BACTERIAL AND/OR FUNGAL INFECTION

Abstract

A system for treating and/or preventing a viral, bacterial and/or fungal infection in the oral cavity and/or along the respiratory tract, in particular the interior of the nose, throat, trachea and/or lungs, of a patient by reactive species generated by plasma as well as a plasma for such use is disclosed. The system comprises a plasma source generating reactive species in a gas, the plasma source being configured to be located outside a body of the patient, and a species directing member forming at least one duct for guiding at least a part of the reactive species generated by the plasma source into the oral cavity and/or the respiratory tract.

Claims

1-15. (canceled)

16. A system for treating or preventing a viral, bacterial or fungal infection in the oral cavity or along the respiratory tract of a patient by reactive species generated by plasma, the system comprising: a plasma source generating reactive species in a gas, the plasma source being configured to be located outside a body of the patient; and a species directing member forming at least one duct to guide at least a part of the reactive species generated by the plasma source into at least one of the oral cavity and the respiratory tract, wherein the plasma source comprises a first electrode in the form of a laminar shaped high-voltage electrode.

17. The system of claim 16, wherein the viral, bacterial or fungal infection is in the interior of the nose, throat, trachea or lungs of the patient.

18. The system of claim 16, wherein the duct comprises: a first end through which at least part of the reactive species generated by the plasma source enter the duct; and a second, open end through which at least part of said reactive species are released, wherein the first end is configured to be located outside the patient's body and the second end is configured to be located in the oral cavity or in the respiratory tract.

19. The system of claim 18, wherein the duct is at least partly formed by an elongate tubular member, wherein the tubular member has a length of at least 1 cm.

20. The system of claim 18, wherein the tubular member has a length of at least 10 cm.

21. The system of claim 18, wherein the tubular member has a length of at least 30 cm.

22. The system of claim 16, wherein the plasma source comprises the first electrode, a second electrode and a dielectric member, wherein at least a part of the dielectric member is disposed between the first electrode and the second electrode, wherein the second electrode is a structured ground electrode.

23. The system of claim 22, wherein the second electrode is a mesh or comb shaped electrode.

24. The system of claim 16, wherein the plasma source forms a duct-shaped portion through which the gas flows, wherein a first electrode of the plasma source is a part of the duct-shaped portion or constitutes the duct-shaped portion

25. The system of claim 24, wherein a second electrode of the plasma source is arranged along a main axis of the duct.

26. The system of claim 16, further comprising a chamber disposed between the plasma source and the species directing member, wherein the chamber comprises a chamber outlet opening, and wherein a first end of the species directing member is fluidly connected to the chamber outlet opening.

27. The system of claim 26, wherein the chamber is formed in a chamber member, wherein the chamber member is manually detachable from the plasma source or manually removably connectable to the plasma source.

28. The system of claim 27, wherein the chamber member is manually detachable from the plasma source or manually removably connectable to the plasma source via a snap-fit or friction-fit connection.

29. The system of claim 26, further comprising a gas flow generator configured to generate at least one of a gas flow through the species directing member and a gas flow into the chamber.

30. The system of claim 29, wherein the gas flow generator is a fan.

31. The system of claim 29, wherein the gas flow generator is positioned outside the chamber.

32. The system of claim 31, wherein the gas flow generator is positioned outside the chamber upstream of the chamber.

33. The system of claim 16, further comprising a gas source.

34. The system of claim 33, wherein the gas is pressurized in the gas source.

35. The system of claim 16, wherein the system is a hand-held device.

36. A method for treatment or prevention of at least one of a viral, bacterial or fungal infection in the oral cavity or along the respiratory tract of a patient, wherein the method comprises: providing a device in accordance with claim 16; generating reactive species in a gas with a plasma source of the device being located outside a body of the patient; guiding at least a part of the reactive species generated by the plasma source into at least one of the oral cavity and the respiratory tract.

37. The method of claim 36, wherein said viral infection is a viral infectious disease selected from the group consisting of infections by coronaviruses, influenza viruses, parainfluenza viruses, respiratory syncytial viruses (RSV), rhinoviruses, adenoviruses, noroviruses, enteroviruses, human metapneumoviruses, herpesviruses.

38. The method of claim 37, wherein the coronaviruses are SARS-CoV, SARS-CoV-2, MERS.

39. The method of claim 37, wherein the herpesviruses are HSV-1, HSV-2, VZV, EBV, HCMV, HHV-6, HHV-7, HHV-8.

40. The method of claim 37, wherein said viral infectious disease is the virus infection disease COVID-19 caused by the coronavirus SARS-CoV-2.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0086] The subject-matter of the application will be explained in more detail with reference to preferred exemplary examples which are illustrated in the attached drawing, in which

[0087] FIG. 1 is a schematic perspective view of a system according to a first example.

[0088] FIG. 2 is a schematic cross-sectional view of the system.

[0089] FIG. 3 is a schematic cross-sectional view of a system according to a second example.

[0090] FIG. 4 is a schematic perspective view of a system according to a third example.

[0091] FIG. 5 is a schematic view of a variation of the system illustrated in FIG. 4.

[0092] FIGS. 6a and 6b are schematic views of further examples.

[0093] FIG. 7 is a schematic view of a further example, comprising a bladder.

[0094] FIGS. 8a and 8b illustrate alternative configurations of the plasma source of the system.

[0095] FIGS. 9a to 9g illustrate several examples of electrodes.

[0096] FIG. 10 reports the coronavirus reduction after plasma treatment. The following experiments were conducted: (A) Controls: virus without plasma treatment (no plasma); (B) mock transfection with plasma treated medium (20 μL or 3 μL; in case the CAP secretes cytotoxic compounds into the medium); (C) The coronavirus HCoV-229E was genetically modified to encode renilla luciferase (229E-Rluc). The virus was suspended in DMEM+5% FCS. Caco-2 cells were infected with the treated virus samples. After 48 hours incubation, the cells were lysed and the luciferase activity in the supernatant was determined.

[0097] FIG. 11 is a side view of a modelled upper respiratory system with indications of various volumina.

[0098] FIG. 12 illustrates a cross section of the rima glottidis in an upper respiratory tract (URT) model.

[0099] FIG. 13 illustrates an experimental set-up of microbiological experiments.

[0100] FIG. 14 illustrates results of reduction of bacteria for three selected bacterial strains. Each bar represents the median of nine experiments on three different days. The error bar shows the 25%- and the 75%-quartile. The horizontal line at ordinate value 4 represents the lower detection limit, and the horizontal line at ordinate value 6 the upper detection limit.

[0101] FIGS. 15-19 show diagrams indicating results of ozone measurements and bacteria reductions.

[0102] While the above-identified figures set forth one or more embodiments of the present invention, other embodiments are also contemplated, as noted in the discussion. In all cases, this disclosure presents the invention by way of representation and not limitation. It should be understood that numerous other modifications and embodiments can be devised by those skilled in the art, which fall within the scope and spirit of the principles of the invention. The figures may not be drawn to scale, and applications and embodiments of the present invention may include features, steps, and/or components not specifically shown in the drawings.

DETAILED DESCRIPTION OF EXAMPLES

[0103] Examples according to the present application will be described with reference to the drawings in which identical or similar reference signs designate identical or similar elements. The features of the examples may be combined with each other, unless specifically noted otherwise.

[0104] FIG. 1 shows a schematic view of a system 2 according to a first example. The system is configured for treating and/or preventing a viral, bacterial and/or fungal infection in the oral cavity and/or along the respiratory tract of a patient by reactive species generated by plasma. The system 2 comprises a plasma source 4 generating reactive species in a gas. The plasma source 4 is configured to be located outside the body of the patient.

[0105] The system further comprises a species directing member 6 forming at least one duct for guiding at least a part of the reactive species generated by the plasma source 4 into the oral cavity and/or the respiratory tract of the patient.

[0106] The duct comprises a first end 61 through which at least part of the reactive species generated by the plasma source 4 enter the duct and a second, open end 10 through which at least part of said reactive species are released. The first end 61 of the duct is configured to be located outside the patient's body. The second end 10 of the duct is configured to be located or to be arranged in the oral cavity and/or in the respiratory tract of the patient.

[0107] The duct is preferably at least partly formed by an elongate tubular member 8. The tubular member 8 may be flexible or rigid.

[0108] As illustrated in FIG. 2, the tubular member 8 may have a length 1 and/or an inner diameter d such that the tubular member 8 is suited to be inserted with its second end 10 into the oral cavity and/or a nasal cavity as part of the respiratory tract of the patient. For example, the length of the tubular member 8 may be between 0.5 cm and 10 cm. The tubular member 8 preferably has an inner diameter d of at least 0.2 cm, more preferably at least 0.5 cm.

[0109] The tubular member 8 is preferably made from a polymeric material, for example from a polymeric material comprising silicone and/or polyvinyl chloride. More preferably, the tubular member 8 consists of silicone and/or polyvinyl chloride.

[0110] The plasma source 4 is configured to generate a non-thermal plasma and/or a cold atmospheric plasma and comprises—as schematically illustrated in FIG. 2—a first electrode 12, a second electrode 14 and a dielectric member 16, wherein at least a part of the dielectric member 16 is disposed between the first electrode 12 and the second electrode 14.

[0111] The first electrode 12 is preferably a laminar shaped high-voltage electrode and the second electrode 14 is preferably a structured ground electrode. Preferably, the structure of the second electrode 14 is configured such that the second electrode 14 is suited to generate surface micro discharges for generating the plasma when a voltage is applied to the first electrode 12 and/or the second electrode 14, here preferably to the first electrode 12. The second electrode 14 may be embedded in the dielectric member 16.

[0112] FIGS. 9a to 9g illustrate examples of a electrodes. FIGS. 9a to 9f show plan views showing a first electrode—here indicated by reference sign 7—and a second, structured electrode—here indicated by reference sign 9. The electrodes 7, 9 are separated from each other by a dielectric member (not shown in FIGS. 9a to 9f), as described above. As shown in FIG. 9a, the second electrode 9 may comprise a first segment 21 forming a base from which a plurality of second segments or branches extend. The second segments are electrically coupled to the first segment 21. As illustrated, the first segment 21 may have a linear structure. As shown in FIG. 9a, the second segments may extend parallel, for example as straight lines. Thus, the electrode 9 may be “comb-shaped”. Alternatively, as shown in FIG. 9b, the second segments e.g. may be shaped wavelike or sinusoidally.

[0113] FIG. 9c shows an example of a second electrode 9 having a serpentine shape. FIG. 9e shows an example of an electrode 9 which is spiral shaped, FIG. 9d shows an electrode 9 having the shape of a rectangular spiral. FIG. 9f shows an example of an electrode 7 having a meandering shape.

[0114] FIG. 9g shows—in a perspective view—an electrode having a mesh-shaped structure.

[0115] The first electrode 12 and/or the second electrode 14 may have an electrode surface between 1 cm.sup.2 and 100 cm.sup.2. The electrode surface may be rectangular, for example sized between 1 cm times 1 cm and 10 cm times 10 cm. Different sizes of the electrode surface allow for individual adjustments. For example, a smaller size of the electrode surface may be suited for a child, while a larger size is preferred for a grown-up person.

[0116] The system further comprises an energy source 18 for energizing the plasma source 4 and a control unit 20 configured to control a power supply from the energy source 18 to the plasma source 4. The control unit 20 is preferably configured to adjust a value of a voltage applied to the first electrode 12. Adjusting the voltage allows for an adjustment of the relation between the oxygen-chemistry and the nitrogen chemistry of the plasma, as explained above.

[0117] The system further comprises a chamber 24 disposed between the plasma source 4 and the species directing member 6. The chamber 24 comprises a chamber outlet opening 26. A first end of the species directing member 6, which may be identical to the first end 61 of the duct, is connected to the chamber outlet opening 26. A cross section of the chamber 24 is preferably larger than a cross section of the chamber outlet opening 26 and/or a cross section of the species directing member 6 along a longitudinal axis thereof. In this manner, the plasma source 4 may be provided with a relatively large surface area. This allows to generate a large amount of reactive species in the chamber 24 in a relatively short time.

[0118] The plasma source 4 preferably forms a surface region 28 delimiting at least part of the chamber 24, wherein the reactive species generated by the plasma source 4 are released into the chamber 24. According to this example, at least a portion of the surface region 28 is substantially planar.

[0119] Only the second electrode 14 is preferably exposed to gas in the chamber 24.

[0120] The chamber outlet opening 26 is located, for example, opposite the surface region 28 formed by the plasma source 4 with respect to the interior of the chamber 24. The duct of the species directing member 6 extends from the chamber 24 in a direction substantially perpendicular to the surface region 28. The chamber 24 may have a volume between 3 cm.sup.3 and 100 cm.sup.3.

[0121] The chamber 24 is formed in a chamber member 22. Preferably, the chamber member 22 is manually detachable from the plasma source 4 and/or removably connectable to the plasma source 4, for example via a snap-fit and/or a friction-fit connection.

[0122] According to a variation, the species directing member 6 may further form a second duct for guiding at least a part of the reactive species generated by the plasma source 4 into the oral cavity and/or the respiratory tract of the patient. Thus, the first mentioned duct may, for example, be used for a treatment of the oral cavity, whereas the other duct may, for example simultaneously, be used for a treatment of the nasal cavity.

[0123] As indicated in FIG. 2 by a dash-dotted line, the tubular member may comprise an arcuate shape 8′. The length of the tubular member 8 with such arcuate shape 8′ may range, for example, from 3 cm to 10 cm. For example, the tubular member 8 and/or its arcuate shape 8′ may be in the form of a Guedel Tubus.

[0124] More generally, the tubular 8 may have a length in the order of 1 m or 2 m. As surprisingly found by the inventors, even such a long tubular member is suited to effectively guide at least a part of the reactive species generated by the plasma source 4 to the patient, in particular when an adequate flow is provided therethrough.

[0125] The chamber 24 may comprise one or more gas inlets 32 through which gas flows into the chamber, e.g., ambient air.

[0126] FIG. 3 shows a second example which might be regarded as a variation of the first example. If not otherwise described in the following, the second example can be designed as the first example.

[0127] The system according to the second example comprises a gas flow generator 34, for example in the form of a fan, configured to generate a gas flow 36 through the species directing member 6 to the patient and/or a gas flow into the chamber 24. This is advantageous because the gas flow 36 provides for an effective transportation of the reactive species through the elongate member 8 to the patient.

[0128] Preferably, the system further comprises one or more gas inlets 30 which allow for a gas flow 32 into the chamber 24. As shown in FIG. 3, the one or more inlets 30 may be arranged upstream of the flow generator 34 whereas the outlet 26 of the chamber 24 may be arranged downstream of the flow generator 34. Alternatively, the gas flow could be generated at one or more of the one or more gas inlets 30 and/or after the outlet 26 (e.g., by arranging a fan in the tubular member 8)

[0129] As illustrated in FIG. 3, the gas flow generator 34 may be positioned at least partially within the chamber 24. Alternatively, the gas flow generator 34 may be positioned adjacent to the chamber 24 or in the species directing member 6. For example, the gas flow generator 34 may be positioned at the chamber outlet opening 26 and/or at the first end of the species directing member 6 or the first end 61 of the duct.

[0130] The gas inlet 30 may be configured to direct the gas flow 32 into the chamber 24 in a direction towards the plasma source 4, preferably in a direction towards the surface region 28 formed by the plasma source 4. In the illustrated example, the gas inlet 30 is configured to direct at least part or most of the gas flow 32 into the chamber 24 in a direction substantially parallel to the surface region 28 formed by the plasma source 4.

[0131] FIG. 4 shows a third example. If not otherwise described in the following, the third example can be designed as the first and/or second example.

[0132] The gas inlet 30 of the system according to the third example is configured to direct at least part or most of the gas flow 32 into the chamber 24 in a direction substantially perpendicular to the substantially planar portion of the surface region 28 formed by the plasma source 4.

[0133] As illustrated, the gas inlet 30 may be located opposite to the surface region 28 formed by the plasma source 4 with respect to the interior of the chamber 24. The gas inlet 30 may be in the form of a short tube. The gas may be ambient air.

[0134] The system may further comprise a gas source. For example, as illustrated in FIG. 5, the gas flow generator 34 which is here located outside the chamber 34 may comprise the gas source. The gas source is preferably a source of pressurized gas, where the pressure of the pressurized gas is at least 200 kPa and/or 1000 kPa or less.

[0135] The pressurized gas may be air, O.sub.2, or a mixture of O.sub.2 and N.sub.2, or a mixture of O.sub.2, N.sub.2 and a noble gas, for example Ar and/or He. As indicated above, the oxygen content and the nitrogen content in the gas supplied to the plasma source 4 (e.g., in the pressurized gas) may be varied in order to achieve a desired composition of the reactive species generated by the plasma.

[0136] The system may further comprise a connection tube 40 conducting the gas from the gas source or the gas flow generator 34 to the plasma source 4 or to the chamber 24. Preferably, the connection tube 40 conducts the gas from the gas source into the chamber 24 through the gas inlet 30. In view of normal hospital settings, such connection tube may be, for example, at least 20 cm, at least 50 cm or at least 1 m long.

[0137] The system may further include a flow regulator 35, for example as a part of the flow generator 34, configured to provide for a gas volume flow of at least 0.1 standard liter per minute from the gas source.

[0138] FIGS. 6a and 6b illustrate schematically further examples. The system may further comprise a mechanical ventilator 100, for example in the form of a positive pressure ventilator, where the species directing member is at least partially formed by a ventilation tube 101 for intubating the patient. As illustrated in FIG. 6a, the plasma source 4 may be located outside a housing 102 of the mechanical ventilator 100. Alternatively, as illustrated in FIG. 6b, the plasma source 4 may be located inside the housing 102 of the mechanical ventilator 100. If the plasma source 4 is located outside the housing 102 of the mechanical ventilator 100, the plasma source 4 may be connected to the ventilation tube 101 via a Y connector 103.

[0139] Alternatively, the system may comprise a mechanical ventilator 100, for example a positive pressure ventilator, and the species directing member may be formed as a nasal mask, a nose piece, or a full-face mask (not shown). In this case, the species directing member may, but does not necessarily have to be, configured to extend into the oral cavity and/or the respiratory tract. For example, the reactive species may be guided to the nasal mask, nose piece, or full-face mask (e.g., by being entrained in the pressurized gas from the ventilator or through a separate connection fluidly connected with the nasal mask, nose piece, or full-face mask) and inhaled by the patient when the patient takes a breadth.

[0140] As shown exemplarily in FIG. 6b, the system may further comprise an exhalation tube 104 for receiving exhaled air from the patient. The exhalation tube 104 may be connected to a valve member 105 designed to regulate the direction of the air exhaled by the patient. The valve member 105 may be further connected to the ventilation tube 101 and further designed to regulate the direction of the inhaled air.

[0141] As illustrated, the system may additionally comprise a further plasma source 106, connected to the exhalation tube 104 such that the exhaled air is at least partially led to the further plasma source 106. Thus, one or more pathogens can be inactivated at least partially by the further plasma source 106.

[0142] The system may further comprise a filter 107, preferably arranged downstream the further plasma source 106, for filtering one or more pathogens from the exhaled air. The filter 107 may be provided by a fibrous or porous material.

[0143] FIG. 7 shows an example where the mechanical ventilator comprises a bladder 110. Thus, the reactive species can be conducted from the plasma source 4 via the species directing member 6 into the bladder 110 and further from the bladder 110 via the ventilation tube 101 to the patient. As sketched in FIG. 7, the plasma source 4 may be arranged outside the bladder 110. Alternatively, the plasma source 4 may be arranged within the bladder 110.

[0144] FIGS. 8a and 8b illustrate a further alternate design of the plasma source. The plasma source may form a duct 40 through which the gas flows, wherein a first electrode of the plasma source is a part of the duct 40, constitutes the duct 40, and/or is arranged at least partially around the duct 40. The duct 40 may be shaped cylindrically, for example—as sketched in FIG. 8a—having a circular cross section or—as sketched in FIG. 8b—having a rectangular cross section.

[0145] A second electrode of the plasma source may be arranged at least partly within the duct 40 along a main axis A of the duct 40, e.g. along a longitudinal symmetry axis of the cylinder. Here, preferably the second electrode is a structured electrode. The duct 40 may be directly coupled to the species directing member 6 such that the reactive species generated by the plasma source 4 are guided from the duct 40—for example via or by a gas flow generator 34—directly into the species directing member 6 and through the species directing member 6 to the patient.

[0146] FIG. 10 reports the coronavirus reduction after plasma treatment. The plasma device used in these tests is the one described in this application. The details of the experiment underlying the results shown in FIG. 10 are as follows: The human coronavirus 229E (HCoV-229E) is one of four coronaviruses responsible for the common cold. For the reporter assay, the virus HCoV-229E was genetically modified to encode renilla luciferase. Renilla luciferase is an enzyme that catalyzes the reaction of luciferin with oxygen and ATP to oxyluciferin, CO.sub.2 and AMP. The reaction produces light. When the virus (HCoV-229E) is active and multiplies in infected cells, it also produces renilla luciferase. The light intensity in a sample mixed with the substrate luciferin correlates with the amount of virus. When a substance (here the cold plasma (CAP)) has a viricidal effect, the virus should not be able to replicate in infected cells, so less luciferase and less light is produced. In the experimental setup 3 μl or 20 μL of a HCoV-229E virus solution (3×10{circumflex over ( )}7 pfu/sample) were treated with CAP in a 96-well microtiter plate either for 6 minutes, or two times for 3 minutes. The experimental design was chosen to imitate the behavior of a coronavirus in an organic fluid such as saliva. The results of FIG. 10 report that a 6 minutes CAP treatment led to more than 60% reduction in luciferase activity. These test results indicate that coronaviruses can be inactivated in an organic fluid (e.g., in saliva).

[0147] In the following, some experiments on the reduction of bacteria in the respiratory tract and on the absorption of plasma species by mucous membranes are presented. First, a three-dimensional anatomical model is described on the basis of which bacterial reduction was determined. Then, the experiments to determine the absorption of plasma species by mucous membranes are presented.

Three-Dimensional Anatomical Model of an Area Above a Cuff of Mechanically Ventilated Patients

[0148] The system described herein may be used in the area above the cuff of invasively mechanically ventilated patients with uninjured mucous membranes. At this natural body opening/cavity, the behavior, e.g., the spatial distribution of plasma-activated medical compressed air flowing from the application tubing of the device is influenced by anatomical conditions.

[0149] To generate experimental data demonstrating the safety and efficacy of the system under these conditions, a three-dimensional computer generated model of the area above a cuff of mechanically ventilated adults was created. This model—herein also designated as “upper respiratory tract model” (URT model or simply “model”)—was produced using 3D printing and used in preclinical studies to take into account the geometry in this body region. In addition, various flow simulations were performed using the model. In the following section, the design of the anatomically highly detailed model is described in terms of its use in the experimental setup and in the context of the computer simulation, followed by a more detailed explanation of the data generated with it.

[0150] FIG. 11 shows the side view of the modeled upper airway. Based on the scaled cross-sectional drawings of the upper respiratory tract from literature (Sobotta: Atlas der Anatomie, Elsevier, 2017), a 2D sketch was created using a 3D modeling software (Autodesk Inventor© 3D modeling software). The extension of the model in the vertical direction is based on descriptions from the literature as well as on further anatomical drawings showing the upper respiratory tract in different views. The anatomical structures were precisely measured in the drawings and transferred to the 3D model in the appropriate proportions.

[0151] The anatomical conditions of the upper respiratory tract may naturally differ somewhat from person to person in terms of shape and dimension. For example, the nasal cavity may have more or less pronounced curvatures. However, the shape of the upper respiratory tract, which is regarded as a physical flow channel, does not vary to such an extent that it can be assumed to have a relevant influence on the flow dynamics. Important constrictions and dilatations exist equally in all people. Thus, the model is an exemplary illustration of the adult upper respiratory tract that is believed to adequately reflect the flow conditions. The model was scaled at the end so that the diameter of the trachea is 2 cm, placing the dimension more in the upper reference range of human anatomy (Aumüller, G. et al.: Anatomie, Thieme, 2017).

[0152] FIG. 11 illustrates different sections of the upper respiratory tract in the model, namely a nasal cavity 201, an oral cavity 202, a pharynx, 203, an epiglottic space 204, a glottis 205, a subglottic space 206 and a trachea 207. The volume occupied by the nasal cavity 201 is approximately 31 mL, the volume of the oral cavity 202 approximately 85 mL, the volume of the pharynx 203 approximately 45 mL, the volume of the epiglottic space 204 approximately 8 mL and the volume of the subglottic space 206 approximately 27 mL. The position of an endotracheal cuff 208 is also drawn and should be approximately 1.5 to 2.5 cm below the glottis 205 after successful intubation/tracheotomy (Varshney, M., Kumar, R., Sharma, K. & Varshney, P.: Appropriate depth of placement of oral endotracheal tube and its possible determinants in Indian adult patients, Indian J. Anaesth. 55, 488, 2011). The total volume of the model above the cuff 208 is approximately 175 mL with the mouth wide open. With the mouth closed or slightly open, this volume would be approximately 95 to 115 ml.

[0153] The values for the volume of the model are derived from the dead space volume. The dead space volume only takes into account the ventilated portions of the respiratory tract, at which, however, no gas exchange occurs. It is known that the volume of the dead space below the carina is approximately 70 ml (Kain, M. L., Panday, J. & Nunn, J. F.: THE EFFECT OF INTUBATION ON THE DEADSPACE DURING HALOTHANE ANAESTHESIA, Br. J. Anaesth. 41, 94-102, 1969) and the anatomic dead space volume of the entire respiratory tract is between 150 and 200 ml (Oczenski, W., Andel, H. & Werba, A. Atmen, Atemhilfen: Atemphysiologie und Beatmungstechnik, Thieme, 2012). This results in a dead space of 80 to 130 ml for the respiratory tract above the carina. Considering the dimensions and position of the endotracheal cuff 208, the dead space volume above the cuff 208 is 62 to 115 ml.

[0154] When breathing through the mouth, the nasal cavity 201 and nasopharynx are not ventilated. Similarly, when breathing through the nose, the oral cavity 202 is not ventilated and is therefore not part of the dead space volume described. However, by means of the system both cavities 201, 202 are flooded with cold plasma, so the volumes of the oral and nasal cavities must also be taken into account in order to arrive at the total volume above the cuff 208 mentioned above.

[0155] As an important constriction in the upper airways, emphasis has been put on a detailed modeling of the Rima glottidis. A cross-section of the Rima glottidis is shown in FIG. 12. A relatively wide opening angle of 44° and the widest point of 14 mm were defined such that a commercially available tube can fit comfortably.

[0156] An open mouth was assumed for orally intubated patients. Accordingly, a large opening width of 24 mm has also been selected in the model.

[0157] The mucosal folds of the esophagus are adjacent to each other ventrally and dorsally, so that the lumen is usually collapsed. In addition, the esophagus has circular/longitudinal muscle fibers and a venous plexus that close its lumen and provide a gas-tight seal. For this reason, the transition of the pharynx 203 into the esophagus has been indicated in the model. However, the collapsed lumen has not been considered because it is believed to have no relevance in terms of flow dynamics.

[0158] FIG. 13 shows a cross-section of the model, which was fabricated by 3D printing and used for the preclinical experiments. In addition to the described anatomical structures in the upper respiratory tract, an extension of the flow channel was added to the model in the oropharyngeal area and in the subglottic space in order to be able to place Petri dishes 210 there. Furthermore, the airways are positioned at 30° to the horizontal, which corresponds to a typical positioning of intubated or tracheotomized patients. At selected locations, measurement points for the optical measurement of ozone (a parameter for measuring the generated plasma) were integrated into the model to determine the temporal and spatial distribution of plasma in the respiratory tract in the experiments. For the cell culture experiments, these measurement points were removed from the model. Reference sign 211 designates the URT model, flooded with plasma species, 212 an applicator, 213 an applicator tube, 214 a supply tube (with medical pressurized air) and 215 a housing of the system comprising the plasma source. In an enlarged section, reactive plasma species 216 are sketched.

Determination of Bacterial Reduction in the Three-Dimensional Model of the Respiratory Tract (with Moist Patches)

[0159] In this series of experiments, a defined number of bacteria were inoculated on sterile agar-based culture medium, placed at the appropriate positions in the URT model and then treated with the system. The results of these studies showed in the first step the bactericidal effect of cold atmospheric plasma on the selected strains in a humid environment (agar culture medium). Furthermore, by selecting different bacteria with different characteristics, such as the different cell membrane structure in gram-negative and gram-positive bacteria, a possible selectivity of the effect of the cold atmospheric plasma was be assessed with respect to these differences.

[0160] The optical density at 600 nm of a prepared bacterial suspension of Staphylococcus cohnii (S. cohnii), Escherichia coli (E. coli) or Enterococcus mundtii (E. mundtii) was measured using a spectrophotometer. The aim was to prepare an initial bacterial solution with approx. 108 bacteria per milliliter, of which a defined amount was added to an appropriate culture medium (agar) dish, spread and dried for 30 min at room temperature (sample). Controls were also prepared to accurately determine the initial concentration of the bacterial suspension. For this purpose, the initial bacterial solution was successively diluted by a factor of 105, spread on commercial Mueller-Hinton agar dishes (diameter 9 cm) and dried. Due to the dilution, approx. 100 colony-forming units appear on the Agar plate after incubation at 37° C. for approx. 12 to 24 h.

[0161] The test setup and procedure essentially correspond to the test for determining the ozone concentration as described below. In both experiments the applicator of the system was inserted 2 cm into the mouth opening of the URT model and the flow rate was set to 0.5 l/min.

[0162] In order to perform the experiments in the URT model, a total of three smaller Petri dishes with a diameter of 3.5 cm were filled from a prepared agar dish with a diameter of 9 cm. Thus, the area ratio between the small and large dishes was 15%. This ratio was taken into account when calculating the initial concentration of the bacterial suspension.

[0163] The measurement positions (pharynx and subglottis) of the samples in the URT model are shown in FIG. 13. In addition, to simulate the humid environment, a Petri dish filled with water was placed at the respective free measurement position in each experiment. Each sample was treated with cold atmospheric plasma for 5 min.

[0164] Three runs were performed at each of the measurement positions, using three systems in alternation. This ensured that there was sufficient time for the plasma source to cool down before being used again. In addition, three adequate control runs were performed for both positions. The control agar dishes were placed at the appropriate position and the application tubing was connected to the compressed air without switching on the system. In addition to the agar dish, a Petri dish with water was positioned at the respective free position (pharynx or subglottis) in the model to seal the model at this position and to simulate pharyngeal moisture. Before each subtest, the model was rinsed with water to “wash” any remaining plasma species from the URT model.

[0165] Following plasma treatment, the samples (along with controls) were incubated at 37° C. overnight or for 24 hours in an incubator. By counting the colony-forming units (CFU) on the agar in the small Petri dish, the initial concentration—determined from the control plates—can be used to calculate the log reduction achieved.

[0166] Nine experiments per bacterial strain were performed in total on three different days. The results are shown in FIG. 14, wherein the bar represents the median and the error represents the 25% and 75% quartiles. The log-10 reduction varied between 4.8 and 6.0 for the three bacterial strains. It could be shown that by using the system, bacteria on agar can be reduced by about 5 log levels within 5 min of plasma treatment.

Absorption of Plasma Species By Mucous Membranes

[0167] The above described URT model is believed to represent the anatomical conditions accurately and is thus believed to provide a good approximation to real conditions. For the experiments, the model was lined with patches and immersed in water to simulate humidity in the respiratory tract.

[0168] In a further experiment, the influence of mucous membranes on the absorption of plasma species was investigated. In this further experiment, the bacterial reduction of S. cohnii on Müller-Hinton agar plates was determined. In addition, the ozone concentration at the respective positions in the model was determined spectroscopically.

[0169] In this experiment, a simplified model of the respiratory tract was created and 3D-printed. The model has the same volume of approx. 175 ml but was anatomically less detailed than the URT model described above. The simplified model was essentially configured as an L-shaped duct. The straight segments of the L were provided as an open latticework. Tissue pieces corresponding to different mucous membranes were wrapped around the latticework, thereby simulating a duct lined with the respective tissue.

[0170] Prior to the experiment, peritoneal skin and gastric mucosa from pig and appendix mucosa from cow were prepared. The respective tissue piece was wrapped around the 3D model. For the measuring unit for optical measurement of the ozone concentration, a hole was cut in the tissue at the appropriate position. Cling film and Parafilm© were wrapped around the tissue pieces in order to seal the sections of the model formed as the open latticework. The respective tissue piece was moistened with tap water using a spray bottle before each experiment. Preparation of bacteria by plating of colony-forming units on the Mueller-Hinton agar dish was performed analogously to the experiment testing bacterial reduction as described above.

[0171] For each of the three tissue types, three agar dishes each were treated with the system at both the pharyngeal and subglottic measurement positions, and the ozone concentration was measured. In addition, three agar dishes were positioned in the pharynx for control purposes in the same setup without switching on the system, but with compressed air applied.

[0172] The model was positioned at an angle of 30°. As in the other experiments, the tube of the system was always inserted 2 cm into the mouthpiece of the model and the flow rate was set to 0.5 ml/min. A Petri dish filled with pure water and an agar dish containing plated S. cohnii were always placed at the respective positions in the model (pharynx and subglottis, respectively). The measuring unit was placed in front of the agar dish. The respective bacterial sample was then treated with cold atmospheric plasma for 5 min. For the partial experiments, three different plasma source units were used alternately to ensure sufficient time for cooling down the plasma source between the experiments.

[0173] FIGS. 15-19 show the result of ozone measurement and bacterial reduction for the different tissue types and for reference with Parafilm alone. The reduction of S. cohnii in the pharynx (FIG. 19, position 1) and subglottis (position 2) is shown.

[0174] When comparing the ozone concentrations in the diagram which characterizes the bioframe model with the ozone concentrations in the diagrams using the different tissue types, a slightly reduced mean saturation can be observed at the measurement position in the pharynx, which varies between 150 and 250 ppm. This reduction in ozone concentration is relatively small and must not necessarily be due to absorption by the tissue, but may also be due to variations in the amount of plasma delivered by the system.

[0175] The situation is different in the subglottis. Here, the ozone concentration for the outer gastric skin as well as the appendix mucosa is about 50 ppm and is thus approximatly 70% lower than the ozone concentration when using Parafilm., This difference is probably related to the use of the agar dishes rather than caused by the different tissue types. Empty Petri dishes were used in the characterization of the model, however, it is believed that that the agar medium may be absorbing a large part of the ozone in the subglottis, resulting in an ozone concentration—as in this experiment—of only 50 ppm.

[0176] When using gastric mucosa, no ozone could be measured in the subglottis. This is also reflected in the corresponding experiment testing microbial reduction as described above where no reduction of bacteria on the agar plates could he detected in this experimental setting, suggesting that the absence of measurable ozone is probably not caused by a measurement error. It should be noted, however, that in this experiment, a much thicker section of gastric mucosa was used for the area in the subglottis, in which the outer gastric skin was not dissected away but still attached to the gastric mucosa. It is therefore conceivable that the thicker tissue section was accompanied by a higher ozone absorption. Considering the results of the other experiments in which no or only very low absorption took place, this is, however, considered rather unlikely as a cause. An alternative reason could be that the mucosa in the bioframe model was not only wall-forming but also protruded unfavorably into the lumen and thus prevented flow or gas exchange.

[0177] In summary the experiments showed that, except for the experimental setting using gastric mucosa in the subglottis, a good reduction of bacteria was always achieved which is comparable to the previous results of the URT model.

[0178] While the invention has been described in detail in the drawings and forgoing description, such description is to be considered illustrative or exemplary and not restrictive. Variations to the disclosed examples can be understood and effected by those skilled in the art and practicing the claimed invention, from a study of the drawings, the disclosure, and the appended claims. In the claims, the word “comprising” does not exclude other elements or steps, and the indefinite article “a” or “an” does not exclude a plurality. The mere fact that certain elements or steps are recited in distinct claims does not indicate that a combination of these elements or steps cannot be used to advantage, specifically, in addition to the actual claim dependency, any further meaningful claim combination shall be considered disclosed.

[0179] The invention relates, for example, to the following aspects:

[0180] 1. A system for treating and/or preventing a viral, bacterial and/or fungal infection in the oral cavity and/or along the respiratory tract, in particular the interior of the nose, throat, trachea and/or lungs, of a patient by reactive species generated by plasma, the system comprising: [0181] a plasma source generating reactive species in a gas, the plasma source being configured to be located outside a body of the patient, [0182] a species directing member forming at least one duct for guiding at least a part of the reactive species generated by the plasma source into the oral cavity and/or the respiratory tract.

[0183] 2. The system of aspect 1, wherein the duct comprises a first end through which at least part of the reactive species generated by the plasma source enter the duct and a second, open end through which at least part of said reactive species are released, preferably wherein the first end is configured to be located outside the patient's body and/or the second end is configured to be located in the oral cavity and/or in the respiratory tract.

[0184] 3. The system of aspect 1 or 2, wherein the duct is at least partly formed by an elongate tubular member.

[0185] 4. The system of any of the preceding aspects, wherein the tubular member has an arcuate shape.

[0186] 5. The system of aspect 4, wherein the tubular member is a Guedel Tubus.

[0187] 6. The system of any of aspects 3 to 5, wherein the tubular member is flexible or rigid.

[0188] 7. The system of any of aspects 3 to 6, [0189] wherein the tubular member has a length of at least 1 cm, at least 2 cm, at least 3 cm, at least 5 cm, at least 10 cm, or at least 30 cm; and/or [0190] wherein the tubular member has a length of less than 30 cm or less than 10 cm.

[0191] 8. The system of any of aspects 3 to 7, wherein the length of the tubular member is between 10 cm and 500 cm, between 10 cm and 400 cm, or between 20 cm and 200 cm.

[0192] 9. The system of any of aspects 3 to 8, wherein the tubular member has an inner diameter of at least 0.2 cm, at least 0.5 cm, at least 1 cm, at least 1.5 cm, or at least 2 cm.

[0193] 10. The system of any of aspects 3 to 9, wherein the tubular member is made from a polymeric material, preferably wherein the material comprises silicone and/or polyvinyl chloride, more preferably wherein the tubular member consists of silicone and/or polyvinyl chloride.

[0194] 11. The system of any of the preceding aspects, wherein the plasma source generates a non-thermal plasma and/or a cold atmospheric plasma.

[0195] 12. The system of any of the preceding aspects, wherein the plasma source comprises a first electrode, a second electrode and a dielectric member, wherein at least a part of the dielectric member is disposed between the first electrode and the second electrode.

[0196] 13. The system of aspect 12, wherein the first electrode is a laminar shaped high-voltage electrode and/or wherein the second electrode is a structured ground electrode, for example a mesh or comb shaped electrode.

[0197] 14. The system of aspect 12 or 13, wherein the second electrode is embedded in the dielectric member.

[0198] 15. The system of aspect 12, 13 or 14, wherein the first electrode and/or the second electrode is exposed to gas in the species directing member, preferably wherein only the first electrode or only the second electrode is exposed to gas in the species directing member, in particular only the second electrode.

[0199] 16. The system of any of the preceding aspects, further comprising an energy source for energizing the plasma source and a control unit configured to control a power supply from the energy source to the plasma source.

[0200] 17. The system of aspect 16, wherein the control unit is configured to apply an alternating current and/or voltage to the first electrode.

[0201] 18. The system of any of the preceding aspects, wherein the plasma source forms a duct through which the gas flows, wherein a first electrode of the plasma source is a part of the duct or constitutes the duct.

[0202] 19. The system of aspect 18, wherein a second electrode of the plasma source is arranged along a main axis of the duct, wherein the second electrode is preferably at least partly arranged within the duct.

[0203] 20. The system of aspect 18 or 19, wherein the second electrode is a structured electrode.

[0204] 21. The system of any of the preceding aspects, further comprising a chamber disposed between the plasma source and the species directing member, wherein the chamber comprises a chamber outlet opening, and wherein a first end of the species directing member is connected to the chamber outlet opening, preferably wherein a cross section of the chamber is larger than a cross section of the chamber outlet opening and/or a cross section of the species directing member along a longitudinal axis thereof.

[0205] 22. The system of aspect 21, wherein the plasma source forms a surface region delimiting at least part of the chamber, wherein the reactive species generated by the plasma source are released into the chamber, preferably wherein at least a portion of the surface region is substantially planar or a tubular segment or circumferential; and/or [0206] wherein the first electrode and/or the second electrode is exposed to gas in the chamber, preferably wherein only the first electrode or only the second electrode is exposed to gas in the chamber.

[0207] 23. The system of aspect 22, wherein the chamber outlet opening is opposite the surface region formed by the plasma source with respect to the interior of the chamber; and/or wherein the duct of the species directing member extends from the chamber in a direction substantially perpendicular or oblique or parallel to the surface region, preferably in a direction substantially perpendicular or oblique or parallel to the substantially planar portion of the surface region.

[0208] 24. The system of any of aspects 21 to 23, wherein the chamber has a volume of at least 3 cm.sup.3.

[0209] 25. The system of any of aspects 21 to 24, wherein the chamber has a volume of at least 5 cm.sup.3.

[0210] 26. The system of any of aspects 21 to 25, wherein the chamber has a volume of at least 10 cm.sup.3.

[0211] 27. The system of any of aspects 21 to 26, wherein the chamber has a volume of 100 cm.sup.3 or less.

[0212] 28. The system of any of aspects 21 to 27, wherein the chamber has a volume of 50 cm.sup.3 or less.

[0213] 29. The system of any of aspects 21 to 28, wherein the chamber has a volume of 30 cm.sup.3 or less.

[0214] 30. The system of any of aspects 21 to 29, wherein the chamber is formed in a chamber member, preferably wherein the chamber member is detachable from the plasma source and/or removably connectable to the plasma source, more preferably manually detachable and/or manually connectable, for example via a snap-fit and/or friction-fit connection.

[0215] 31. The system of aspect 30, wherein the chamber member comprises a radio-frequency identification tag.

[0216] 32. The system of any of aspects 21 to 31, wherein the chamber member comprises a gas inlet allowing a gas flow into the chamber.

[0217] 33. The system of any of the preceding aspects, further comprising a gas flow generator configured to generate a gas flow through the species directing member and/or a gas flow into the chamber.

[0218] 34. The system of aspect 33, wherein the gas flow generator is a fan, in particular a fan with an impeller.

[0219] 35. The system of aspect 33 or 34, wherein the gas flow generator is positioned at least partially within the chamber or adjacent to the chamber; or [0220] wherein the gas flow generator is positioned in the species directing member.

[0221] 36. The system of any of aspects 33 to 35, wherein the gas flow generator is positioned at the chamber outlet opening and/or at the first end of the species directing member.

[0222] 37. The system of any of aspects 33 to 36, wherein the gas flow generator is positioned outside the chamber, preferably upstream of the chamber.

[0223] 38. The system of any of aspects 32 to 37, wherein the gas inlet is configured to direct the gas flow into the chamber in a direction towards the plasma source, preferably in a direction towards the surface region formed by the plasma source.

[0224] 39. The system of aspect 38, wherein the gas inlet is configured to direct at least part or most of the gas flow into the chamber in a direction substantially perpendicular or oblique or parallel to the substantially planar portion of the surface region formed by the plasma source.

[0225] 40. The system of aspect 38 or 39, wherein the gas inlet is located opposite or lateral to the surface region formed by the plasma source with respect to the interior of the chamber.

[0226] 41. The system of aspect 38, 39 or 40, wherein the gas inlet is located adjacent the chamber outlet opening.

[0227] 42. The system of any of the preceding aspects, wherein the gas is ambient air.

[0228] 43. The system of any of aspects 1 to 42, further comprising a gas source, preferably a source of pressurized gas.

[0229] 44. The system of aspect 40, wherein the pressure of the pressurized gas is at least 200 kPa.

[0230] 45. The system of aspect 40 or 41, wherein the pressure of the pressurized gas is 1000 kPa or less.

[0231] 46. The system of aspect 43, 44 or 45, wherein the pressurized gas is air or O.sub.2, or a mixture of O.sub.2 and N.sub.2, or a mixture of O.sub.2, N.sub.2 and Ar or a noble gas, for example He.

[0232] 47. The system of any of aspects 40 to 43, wherein the gas in the gas source comprises at least 40% wt of oxygen, preferably at least 50% wt, at least 70% wt, or at least 90% wt of oxygen.

[0233] 48. The system of any of aspects 40 to 43, wherein the gas in the gas source comprises at least 80% wt of nitrogen, at least 85% wt of nitrogen, at least 90% wt of nitrogen or at least 95% wt of nitrogen.

[0234] 49. The system of any of aspects 40 to 44, further comprising a connection tube conducting the gas from the gas source to the plasma source, preferably wherein the connection tube conducts the gas from the gas source into the chamber through the gas inlet.

[0235] 50. The system of any of the preceding aspects, further including a flow regulator.

[0236] 51. The system of aspect 50, wherein the flow regulator is configured to provide for a gas volume flow of at least 0.1 standard liter per minute from the gas source.

[0237] 52. The system of aspect 50, wherein the flow regulator is configured to provide for a gas volume flow of at least 0.3 standard liter per minute from the gas source.

[0238] 53. The system of aspect 50, 51 or 52, wherein the flow regulator is configured to provide for a gas volume flow of 1.0 standard liter per minute or less from the gas source.

[0239] 54. The system of aspect 50, 51 or 52, wherein the flow regulator is configured to provide for a gas volume flow of 0.8 standard liter per minute or less from the gas source.

[0240] 55. The system of any of the preceding aspects, further comprising an exhalation tube for receiving exhaled air from the patient.

[0241] 56. The system of aspect 55, wherein the exhaled air is led to a further plasma source of the system in order to at least partially inactivate one or more pathogens in the exhaled air.

[0242] 57. The system of aspect 55 or 56, further comprising a filter for filtering one or more pathogens from the exhaled air, preferably wherein the filter is an air filter provided by a fibrous or porous material.

[0243] 58. The system of aspect 57, wherein the further plasma source is located upstream of the filter.

[0244] 59. The system of any of aspects 55 to 58, further comprising a filter for absorbing or adsorbing at least part of the reactive species within the exhaled air.

[0245] 60. The system of any of the preceding aspects, wherein the system is a hand-held device.

[0246] 61. The system of any of the preceding aspects, further comprising a mechanical ventilator, preferably a positive pressure ventilator, wherein the species directing member is at least partially formed by a ventilation tube for intubating the patient.

[0247] 62. The system of aspect 61, wherein the plasma source is located inside a housing of the mechanical ventilator.

[0248] 63. The system of aspect 61 or 62, wherein the mechanical ventilator comprises a bladder, wherein the reactive species generated by the plasma source are conducted into the bladder.

[0249] 64. The system of aspect 61, wherein the plasma source is located outside a housing of the mechanical ventilator, wherein the plasma source is connected to the ventilation tube via a Y connector.

[0250] 65. The system according to any of the preceding aspects, further comprising an expandable cuff configured to restrict airflow through the respiratory tract, preferably wherein the cuff is configured to be expanded at a position distal from the second end of the species directing member.

[0251] 61. Use of the system according to any of the preceding aspects for plasma treatment of a viral, bacterial and/or fungal infection in the oral cavity and/or along the respiratory tract in a patient.

[0252] 62. A method for plasma treatment of a viral, bacterial and/or fungal infection in a patient comprising introducing the species directing member (6) of the system according to any of the preceding aspects into the respiratory tract, in particular into the interior of the nose, the throat, trachea and/or lungs, and/or into the oral cavity.

[0253] 63. The method according to aspect 62, wherein the species directing member (6) is inserted less than 1 cm or less than 0.5 cm into the nose and/or wherein the species directing member (6) is inserted less than 10 cm, preferably less than 5 cm into the pharyinx.

[0254] 64. Plasma as obtainable by the system according to any of the preceding aspects for use in medicine.

[0255] 65. Plasma as obtainable by the system according to any of the preceding aspects for use in the treatment and/or prevention of a viral, bacterial and/or fungal infection in a patient.

[0256] 66. Plasma for use in the treatment and/or prevention of a viral, bacterial and/or fungal infection in a patient.

[0257] 67. The use according to aspect 61, the method according to aspect 62 or 63, or the plasma for use according to aspect 64, 65 or 66, wherein said viral infection to be treated and/or prevented is a viral infectious disease selected from the group consisting of infections by coronaviruses, preferably SARS-CoV, SARS-CoV-2, MERS; influenza viruses, parainfluenza viruses, respiratory syncytial viruses (RSV), rhinoviruses, adenoviruses, noroviruses, enteroviruses, human metapneumoviruses, herpesviruses, preferably HSV-1, HSV-2, VZV, EBV, HCMV, HHV-6, HHV-7, HHV-8.

[0258] 68. The use according to aspect 61 or 67, the method according to aspect 62, 63 or 67, or the plasma for use according to any aspects of 64 to 67, wherein said viral infection is the virus infection disease is the virus infection disease caused by the severe acute respiratory syndrome coronavirus (SARS-CoV)-2, SARS-CoV-1, or Middle East respiratory syndrome coronavirus (MERS-CoV), preferably the virus infection disease COVID-19 caused by the coronavirus SARS-CoV-2.

[0259] 69. The use according to aspect 61, the method according to aspect 62 or 63, or the plasma for use according to aspect 64, 65 or 66, wherein said bacterial infection is caused by gram-positive and/or gram-negative bacteria.

[0260] 70. The use according to aspect 61 or 69, the method according to aspect 62 or 63, or the plasma for use according to aspect 64, 65 or 66, wherein said bacterial infection is caused by Staphylococcus cohnii (S. cohnii), Escherichia coli (E. coli) and/or Enterococcus mundtii (E. mundtii).

[0261] 71. The use according to aspect 61 or 67 to 70, the method according to aspect 62, 63, 67 to 70, or the plasma for use according to any aspects of 64 to 70, wherein the system is inserted into the respiratory tract, in particular into the interior of the nose, the throat, trachea and/or lungs, and/or into the oral cavity with reactive species being generated by the plasma source at least twice a day for at least 2 minutes.

[0262] 72. The use according to aspect 61 or 67 to 70, the method according to aspect 62, 63, 67 to 70, or the plasma for use according to any aspects of 64 to 70, wherein the system is inserted into the respiratory tract, in particular into the interior of the nose, the throat, trachea and/or lungs, and/or into the oral cavity with reactive species being generated by the plasma source at least twice a day for 5 minutes.