Antipathogenic compositions and methods thereof

Abstract

To provide compositions, devices and methods for inactivating viruses, bacteria and fungi.SOLUTION: The compositions, methods and devices include coatings or slurries, such as silicon nitride powder coatings or slurries, for inactivation of viruses, bacteria and / or fungi.SELECTED DRAWING: None

Description

[Technical field]

[0001] The present disclosure relates to antiviral, antibacterial, and antifungal compositions, systems, methods, and devices. More specifically, the present disclosure relates to silicon nitride compositions, devices, and coatings for the inactivation and lysis of viruses, bacteria, and fungi. [Background technology]

[0002] The need for safe and reliable inactivation, removal, or lysis of viruses, bacteria, and fungi is universal. There is a widespread need to control pathogens that affect human health and agricultural products. There is a need for materials with anti-pathogenic properties for human drug therapy, as well as for use as surface coatings and / or composite materials for various medical devices or equipment, examination tables, clothing, filters, masks, gloves, catheters, endoscopic instruments, etc.

[0003] Furthermore, the application of anti-pathogenic materials is greatly needed in agriculture. Up to 15% of the world's annual food crops are devastated due to their susceptibility to plant-based viruses, bacteria, and fungi. For example, Plasmopara viticola is considered one of the most devastating diseases of grapevines under relatively warm and humid summer climates, causing significant reductions in crop yields in France, Spain, and Italy. Furthermore, there is growing concern that mycotoxins produced by these fungi have an overall negative impact on human health and lifespan. Traditional pharmaceutical pathogen inactivation methods include the use of specially engineered organic petrochemicals, the use of antibiotics, the use of genetic engineering, or via the use of solid inactivating agents (e.g., cuprous oxide Cu2O and silver nitrate AgNO3). While these therapies are fairly effective, there are significant environmental health and safety concerns with their use. New petrochemical compounds can have long-term residual effects on humans, wildlife, plants, and soil. Heavy use of antibiotics in humans, animals, and agricultural crops increases inherent bacterial pathogen resistance. Genetic engineering of crops to resist disease is increasingly unpopular and politically untenable. Solid inactivators release Cu and Ag ions that can induce damage to mammalian cells. In addition, each of these approaches to pathogen control is subject to increased regulatory scrutiny.

[0004] Thus, there is a need for a safe and reliable method for inactivating and killing viruses, bacteria, and fungi that can be applied to medical devices, equipment, clothing, or other systems that may be in prolonged contact with the human body or that may be used in various agricultural applications to treat viral or bacterial diseases and fungal infections. Summary of the Invention [Means for solving the problem]

[0005] Provided herein is a device having silicon nitride on at least a portion of a surface of the device, the silicon nitride being present in a concentration sufficient to inactivate pathogens on the surface of the device. The device may include a silicon nitride coating. The silicon nitride may be present in a concentration of about 1% to about 100% by weight, e.g., 15% by weight of silicon nitride. Also provided herein is a method of treating or preventing pathogens at a location within a human patient. The method may include contacting the patient with a device comprising silicon nitride. In another embodiment, the method of inactivating pathogens may include contacting a device comprising silicon nitride at a concentration of about 1% to about 100% by weight with a virus. The method may further include coating the device with silicon nitride powder on the surface of the device and / or incorporating silicon nitride powder into the device. The silicon nitride in the device, the device, and / or the coating may be present in a concentration sufficient to inactivate pathogens. The device may be in contact with the patient for as long as required to inactivate the pathogens. For example, the device may be in contact with the patient for at least one minute or may be permanently implanted within the patient.

[0006] The silicon nitride in the device or apparatus can be in the form of a powder. In one embodiment, the pathogen can be influenza A. The silicon nitride can reduce the virus activity by alkaline transesterification and reduce hemagglutinin activity.

[0007] The composition for inactivating pathogens may include silicon nitride at a concentration of about 1% to about 30% by volume, for example, about 1.5% by volume of silicon nitride. In another embodiment, the method for inactivating pathogens may include contacting the pathogen with a composition including silicon nitride at a concentration of about 1% to about 30% by volume. The method may further include spraying the composition onto a surface of a plant to contact the pathogen. The composition may contact the pathogen for at least 1 minute. The composition may include a slurry of silicon nitride particles and water.

[0008] The silicon nitride may be present in a concentration sufficient to inactivate the pathogen. The silicon nitride particles may attach to spores of the pathogen. The pathogen may be Plasmopara viticola. The plant may be Cabernet Sauvignon or Cannonau.

[0009] Further provided herein is a method of treating or preventing a pathogen at a location within a plant. The method may include contacting the plant with a slurry comprising silicon nitride. The slurry may include about 1% to about 30% by volume of silicon nitride. The silicon nitride may be present in a concentration sufficient to inactivate the pathogen. In some embodiments, the pathogen is Plasmopara viticola and the plant is Cabernet Sauvignon or Cannonau. The composition may be in contact with the pathogen for at least 1 minute.

[0010] Other embodiments and iterations of the invention are described more fully below.

[0011] The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee. [Brief description of the drawings]

[0012] [Figure 1] FIG. 1 is an explanatory diagram of influenza A virus. [Figure 2A] FIG. 13 is an illustration of viruses exposed to 0 wt%, 7.5 wt%, 15 wt%, and 30 wt% Si3N4 for 10 minutes. [Figure 2B] FIG. 2B is an illustration of the method used to determine the viability of virus-inoculated cells exposed to Si3N4 from FIG. 2A. [Figure 3A] FIG. 13 is an illustration of viruses exposed to 15 wt % Si3N4 for 1, 5, 10, and 30 minutes. [Figure 3B]FIG. 3B is an illustration of the method used to determine the survival rate of the virus after exposure to Si3N4 according to FIG. 3A. [Figure 4A] 2B is a graph of PFU / 100 μL of influenza A exposed to 0 wt %, 7.5 wt %, 15 wt %, and 30 wt % Si 3 N 4 from FIG. 2A for 10 minutes. [Figure 4B] 2C is a graph of cell viability of influenza A-inoculated cells exposed to 7.5 wt %, 15 wt %, and 30 wt % Si 3 N 4 from FIG. 2B for 10 minutes. [Diagram 5] Photographs of cells inoculated with different ratios of virus to slurry exposed to various concentrations of Si3N4 are included. [Figure 6] (a) Fluorescence microscopy images of MDCK cells before inoculation, (b) after inoculation with virus exposed to control, and (c) after inoculation with virus exposed to 30 wt% Si3N4 are shown. [Figure 7A] 1 is a graph of PFU / 100 μL of influenza A exposed to 15 wt % Si 3 N 4 at room temperature for 1 minute, 5 minutes, 10 minutes, or 30 minutes. [Figure 7B] 1 is a graph of cell viability of influenza A-inoculated cells exposed to 15 wt % Si 3 N 4 at room temperature for 1 minute, 5 minutes, 10 minutes, or 30 minutes. [Figure 8A] 1 is a graph of PFU / 100 μL of influenza A exposed to 15 wt % Si 3 N 4 for 1 minute, 5 minutes, 10 minutes, or 30 minutes at 4° C. [Figure 8B] 4 is a graph of cell viability for influenza A inoculated cells exposed to 15 wt % Si3N4 for 1 minute, 5 minutes, 10 minutes, or 30 minutes at 4° C. [Figure 9] (a) Raman spectrum of influenza A virus before inactivation. (b) Changes in the Raman spectrum of influenza A virus related to chemical modifications of RNA and hemagglutinin after inactivation after 1 min of exposure. [Figure 10]We show that NH3 inactivates influenza A virus via an alkaline transesterification mechanism. [Figure 11] 1 shows OPO extension at the pentacoordinate phosphate group after inactivation. [Figure 12A] The vibrational modes of methionine in the hemagglutinin structure are shown. [Figure 12B] 1 shows the conformational change of methionine in the presence of ammonia. [Figure 13] CS extension of methionine to homocysteine ​​after inactivation is shown. [Figure 14A] 1 is a graph of PFU / 100 μl of feline calicivirus exposed to 15% or 30% by weight Si 3 N 4 for 1 minute, 10 minutes, or 30 minutes. [Figure 14B] 1 is a graph of cell viability of feline calicivirus-inoculated cells exposed to 30 wt % Si 3 N 4 for 1 minute, 10 minutes, 30 minutes, or 60 minutes. [Figure 15A] 1 shows H1H1 influenza A virus (nucleoprotein, NP) stained red after exposure to a 15 wt % silicon nitride slurry for 10 minutes and after inoculation into a biological medium containing MDCK cells stained green for the presence of filamentous actin (F-actin) protein. [Figure 15B] NP stained H1H1 influenza A virus from FIG. 15A is shown. [Figure 15C] F-actin stained MDCK cells from FIG. 15A are shown. [Figure 16A] 1 shows H1H1 influenza A virus (nucleoprotein, NP) stained red without exposure to silicon nitride and after inoculation into vital medium containing MDCK cells stained green for the presence of filamentous actin (F-actin) protein. [Figure 16B] NP stained H1H1 influenza A virus from FIG. 16A is shown. [Figure 16C] Shown are F-actin stained MDCK cells from FIG. 16A. [Figure 17]Cabernet Sauvignon leaves inoculated with Plasmopara viticola are shown, untreated (a) and treated with 1.5 vol.% Si3N4 powder for 1 min (b). [Figure 18A] Untreated sporangia are shown. [Figure 18B] 4 shows sporangia in the presence of Si3N4. [Figure 19] 1 is a graph of control and treated Cabernet Sauvignon and Cannonau leaf area infected with Plasmopara viticola. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0013] Various embodiments of the present disclosure are discussed in detail below. Although specific implementations are discussed, it should be understood that this is done for illustrative purposes only. Those skilled in the relevant art will understand that other components and configurations may be used without departing from the spirit and scope of the present disclosure. Therefore, the following description and drawings are illustrative and should not be construed as limiting. Numerous specific details are described to provide a thorough understanding of the present disclosure. However, in certain instances, well-known or conventional details are not described in order to avoid obscuring the description. Reference to one embodiment or an embodiment in the present disclosure may be a reference to the same embodiment or any embodiment, and such reference means at least one of those embodiments.

[0014] Reference to "one embodiment" or "an embodiment" means that a particular feature, structure, or characteristic described in connection with that embodiment is included in at least one embodiment of the present disclosure. The appearances of the phrase "in one embodiment" in various places in the specification do not necessarily all refer to the same embodiment or to mutually exclusive separate or alternative embodiments of other embodiments. Furthermore, various features are described that may be exhibited by some embodiments and not by other embodiments.

[0015] The term "apparatus" as used herein includes compositions, devices, surface coatings, and / or composites. In some examples, the apparatus may include various medical devices or instruments, examination tables, clothing, filters, masks, gloves, catheters, endoscopic instruments, etc. The apparatus may be metallic, polymeric, and / or ceramic (e.g., silicon nitride and / or other ceramic materials).

[0016] The terms used herein generally have their ordinary meanings in the art, within the context of this disclosure, and within the specific context in which each term is used. Alternative language and synonyms may be used for any one or more of the terms discussed herein, and no special emphasis should be placed on whether a term is detailed or discussed herein. In some cases, synonyms of a particular term are provided. The descriptive detailing of one or more synonyms does not preclude the use of other synonyms. The use of examples anywhere in this specification, including examples of any term discussed herein, is illustrative only and is not intended to further limit the scope and meaning of the disclosure or examples of any term. Similarly, this disclosure is not limited to the various embodiments provided herein.

[0017] Additional features and advantages of the present disclosure will be set forth in the description which follows, and in part will be apparent from the description, or may be learned by practice of the principles disclosed herein. The features and advantages of the present disclosure may be realized and obtained by means of the instruments and combinations particularly pointed out in the appended claims. These and other features of the present disclosure will become more fully apparent from the following description and the appended claims, or may be learned by practice of the principles described herein.

[0018] Provided herein are anti-pathogenic devices, compositions, and apparatuses that include silicon nitride (Si3N4) for inactivation of viruses, bacteria, and fungi.Silicon nitride is biocompatible and has a unique surface chemistry that offers several biomedical applications, including: 1) simultaneous bone formation, osteoinduction, osteoconduction, and bacteriostasis in spinal and dental implants, etc.; 2) killing of bacteria, both gram-positive and gram-negative, following different mechanisms; 3) inactivation of human and animal viruses, bacteria, and fungi, as well as plant-based viruses, bacteria, and fungi; and 4) polymer or metal matrix composites containing silicon nitride powder, natural or artificial fibers, polymers, or metals retain important silicon nitride bone repair, bacteriostatic, antiviral, and antifungal properties.

[0019] In one embodiment, the antipathogenic composition may include silicon nitride. For example, the antipathogenic composition may include silicon nitride powder. In some embodiments, the antipathogenic composition may be a monolithic component that includes 100% silicon nitride. Such a component may be fully dense with no internal porosity, or may be porous with a porosity ranging from about 1% to about 80%. The monolithic component may be used as a medical device or may be used within an apparatus where inactivation of viruses, bacteria, and / or fungi may be desired. In another embodiment, the antipathogenic composition may be incorporated within a device or coating to inactivate viruses, bacteria, and fungi. In some embodiments, the antipathogenic composition may be a slurry that includes silicon nitride powder. For example, the antipathogenic composition may be sprayed onto the surface of a plant for inactivation of agricultural pathogens.

[0020] In some embodiments, the anti-pathogenic composition may inactivate human viruses, bacteria, and / or fungi. Non-limiting examples of viruses that may be inactivated by the anti-pathogenic composition include influenza A and feline calicivirus. For example, silicon nitride bioceramics may be effective in inactivating influenza A viruses. In some embodiments, silicon nitride coatings may reduce antibacterial and antiviral resistance and / or promote bone tissue repair. In some embodiments, the anti-pathogenic composition may inactivate agricultural viruses, bacteria, and / or fungi. Non-limiting examples of agricultural fungi that may be inactivated by the anti-pathogenic composition include Plasmopara viticola (downy mildew) or similar plant pathogens.

[0021] Without being limited to a particular theory, silicon nitride may provide a surface chemistry such that ammonia (NH3) is available for viral, bacterial, or fungal inactivation. The surface chemistry of silicon nitride may be illustrated as follows: Si3N4+6H2O→3SiO2+4NH3 SiO2+2H2O→Si(OH)4

[0022] Nitrogen dissolves faster (within minutes) than silicon, due to the relative stability of surface silanols. For viruses, it has been surprisingly found that silicon nitride can provide RNA cleavage by alkaline transesterification, which leads to loss of genome integrity and virus inactivation. This can also reduce the activity of hemagglutinin.

[0023] In one embodiment, the antipathogenic composition may exhibit elution kinetics that show (i) slow but continuous elution of ammonia from a solid state rather than from the normal gaseous state, (ii) no damage or adverse effects to cells, and (iii) intelligent elution that increases with decreasing pH. The inorganic nature of silicon nitride may be more beneficial than the use of petrochemical or organometallic fungicides that are known to have residual effects on soils, plants, and their fruits.

[0024] The device or apparatus may include silicon nitride on at least a portion of the surface of the device for antiviral, antibacterial, or antifungal effects. In one embodiment, the device may include a silicon nitride coating on at least a portion of the surface of the device. The silicon nitride coating may be applied to the surface of the device as a powder. In some embodiments, the powder may be micrometer sized. In other embodiments, the silicon nitride may be incorporated within the device. For example, the device may incorporate silicon nitride powder within the body of the device. In one embodiment, the device may be made of silicon nitride.

[0025] The silicon nitride coating may be present on the surface of the device at a concentration of about 1% to about 100% by weight. In various embodiments, the coating may include about 1%, 2%, 5%, 7.5%, 8.3%, 10%, 15%, 16.7%, 20%, 25%, 30%, 33.3%, 35%, or 40% by weight of silicon nitride powder. In at least one example, the coating includes about 15% by weight of silicon nitride. In some embodiments, the silicon nitride may be present in or on the surface of the device or apparatus at a concentration of about 1% to about 100% by weight. In various embodiments, the device or apparatus may comprise about 1%, 2%, 5%, 7.5%, 8.3%, 10%, 15%, 16.7%, 20%, 25%, 30%, 33.3%, 35%, 40%, 50%, 60%, 60% 70%, 80%, 90% to 100% silicon nitride by weight.

[0026] In various embodiments, the device or apparatus comprising silicon nitride for anti-pathogenic properties can be a medical device.Non-limiting examples of the device or apparatus include orthopedic implants, spinal implants, pedicle screws, dental implants, indwelling catheters, endotracheal tubes, colonoscopy endoscopes, and other similar devices.

[0027] In some embodiments, silicon nitride may be incorporated into or applied as a coating to materials or devices for anti-pathogenic properties, such as polymers and textiles, surgical gowns, tubing, clothing, air and water filters, masks, tables such as hospital examination and operating tables, desks, toys, filters such as air conditioning filters, or toothbrushes.

[0028] In other embodiments, the silicon nitride powder may be incorporated into compositions including, but not limited to, slurries, suspensions, gels, sprays, or toothpastes. In other embodiments, the silicon nitride may be mixed with water along with any suitable dispersants and slurry stabilizers, and then applied by spraying the slurry onto various agricultural plants, fruit trees, vines, grain crops, and the like. For example, the silicon nitride slurry may be sprayed onto fungus-infected grape leaves.

[0029] In one example, the antipathogenic composition can be a slurry of silicon nitride powder and water. The silicon nitride powder can be present in the slurry at a concentration of about 0.1% to about 20% by volume. In various embodiments, the slurry can include about 0.1%, 0.5%, 1%, 1.5%, 2%, 5%, 10%, 15%, or 20% by volume of silicon nitride.

[0030] Further provided herein is a method of inactivating pathogens by contacting viruses, bacteria, and / or fungi with an anti-pathogenic composition comprising silicon nitride. In one embodiment, the method may include coating a device or apparatus with silicon nitride and contacting the coated apparatus with viruses, bacteria, or fungi. Coating the apparatus may include applying silicon nitride powder to a surface of the apparatus. In other embodiments, the silicon nitride powder may be incorporated into the device or apparatus.

[0031] In further embodiments, the method may include contacting the silicon nitride slurry with a surface of a living agricultural plant, tree, crop, etc., infected with a plant-based pathogen. In one embodiment, the infected leaf may be sprayed with about 1% to about 40% by volume of the silicon nitride slurry in water. The leaf may be exposed to the silicon nitride slurry for at least 1 minute, at least 5 minutes, at least 10 minutes, at least 20 minutes, at least 30 minutes, at least 1 hour, at least 2 hours, at least 5 hours, or at least 1 day. In various examples, the area of ​​the infected leaf may be reduced by at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or at least 99%. In one example, after 1 minute of exposure, the area of ​​the infected leaf may be reduced by about 95%.

[0032] Without being limited to a particular theory, the antipathogenic composition can reduce virus activity and reduce hemagglutinin activity by alkaline transesterification.Surprisingly, it has been found that silicon nitride powder (i) significantly reduces virus activity by alkaline transesterification through the cleavage of RNA internucleotide bond, and (ii) significantly reduces hemagglutinin activity, thus destroying host cell recognition by denaturing protein structure on virus surface, resulting in virus inactivation regardless of the presence of virus envelope.

[0033] In one embodiment, the antipathogenic composition may exhibit elution kinetics that show (i) slow but continuous elution of ammonia from a solid state rather than from the normal gaseous state, (ii) no damage or adverse effects to cells, and (iii) intelligent elution that increases with decreasing pH. Furthermore, the inorganic nature of silicon nitride may be more beneficial than the use of petrochemical or organometallic fungicides that are known to have residual effects on soils, plants, and their fruits.

[0034] Surprisingly, it has also been found that silicon nitride particles can be electrically attracted to and adhere to pathogen spores.

[0035] Also provided herein are methods of treating or preventing a pathogen at a location within a human patient. For example, the pathogen can be a virus, bacteria, or fungus. The method can include contacting the patient with a device, apparatus, or composition comprising silicon nitride. Without being limited to any one theory, silicon nitride inactivates the virus (e.g., influenza A), bacteria, or fungus. The device, apparatus, or composition can include about 1% to about 100% silicon nitride by weight. In some examples, the device or apparatus can include about 1% to about 100% silicon nitride by weight on the surface of the device or apparatus. In one embodiment, the device or apparatus can be a monolithic silicon nitride ceramic. In another embodiment, the device or apparatus can include a silicon nitride coating, such as a silicon nitride powder coating. In another embodiment, the device or apparatus can incorporate silicon nitride into the body of the device. For example, silicon nitride powder can be milled or otherwise incorporated into the body of the device or apparatus using methods known in the art.

[0036] In some embodiments, the device or apparatus may be in contact with the patient for at least 1 minute, at least 5 minutes, at least 30 minutes, at least 1 hour, at least 2 hours, at least 5 hours, or at least 1 day. In at least one example, the device or apparatus may be permanently implanted in the patient.

[0037] Also provided herein is a method of treating or preventing a pathogen at a location within a plant. For example, the pathogen may be a virus, bacteria, or fungus. The method may include contacting the plant with a composition comprising silicon nitride. Without being limited to any one theory, the silicon nitride inactivates the virus, bacteria, or fungus (e.g., Plasmopara viticola). In some embodiments, the composition may include a silicon nitride slurry in water containing up to 40% by volume of silicon nitride with suitable dispersants and slurry stabilizers. The composition may be applied to live agricultural plants, trees, crops, etc., to inactivate, kill, or inhibit the growth of viruses, bacteria, and fungi after contacting the viruses, bacteria, and fungi for at least 1 minute, at least 5 minutes, at least 30 minutes, at least 1 hour, at least 2 hours, at least 5 hours, or at least 1 day. EXAMPLES

[0038] Example 1: Effect of Silicon Nitride Concentration on Viral Inactivation To demonstrate the effect of silicon nitride concentration on virus inactivation, influenza A was exposed to various concentrations of Si3N4 powder. To prepare silicon nitride, a certain weight of silicon nitride powder was mixed with pure distilled water. For example, 7.5 g of silicon nitride was dispersed in 92.5 g of pure distilled water. Virus was added to this mixture at concentrations of 1:1, 1:10, and 1:100, respectively. These mixtures were then incubated at 4°C for 10 minutes with gentle stirring. Influenza A was exposed to 0 wt%, 7.5 wt%, 15 wt%, and 30 wt% Si3N4 for 10 minutes at 4°C, as illustrated in Figure 2A. The mixture was then filtered to remove the silicon nitride powder.

[0039] Then, Madin-Darby canine kidney (MDCK) cells inoculated with influenza A virus were observed for the effectiveness of Si3N4 in inactivating influenza A. After that, the remaining mixture was inoculated into a Petri dish containing live MDCK cells in a biological medium. Then, after 3 days of exposure, the amount of live MDCK cells was counted using a staining method. The viability of MDCK cells was determined after the cells were inoculated with influenza A exposed to Si3N4 for 3 days according to Figure 2B.

[0040] Figure 4A is a graph of PFU / 100 μl of influenza A exposed to 0 wt%, 7.5 wt%, 15 wt%, and 30 wt% Si3N4 for 10 min. Figure 4B is a graph of cell viability of influenza A inoculated cells exposed to 7.5 wt%, 15 wt%, and 30 wt% Si3N4 for 10 min.

[0041] Example 2: Effect of exposure time and temperature on viral inactivation To show the effect of silicon nitride on virus inactivation, influenza A was exposed to a fixed concentration of Si3N4 powder (15 wt%) for various times and at various temperatures. The mixture was then incubated at room temperature and 4 °C for 1 to 30 min with gentle stirring. For example, influenza A was exposed to 15 wt% Si3N4 for 1, 5, 10, or 30 min at room temperature or 4 °C as illustrated in Figure 3A. Madin-Darby canine kidney (MDCK) cells inoculated with influenza A virus were then observed for the effectiveness of Si3N4 in inactivating influenza A. The viability of MDCK cells was determined after the cells were inoculated with influenza A exposed to Si3N4 for 3 days according to Figure 3B.

[0042] Figure 7A is a graph of PFU / 100 μl of influenza A exposed to 15 wt% Si3N4 for 1, 5, 10, or 30 minutes at room temperature, and Figure 7B is a graph of cell viability of influenza A inoculated cells exposed to 15 wt% Si3N4 for 1, 5, 10, or 30 minutes at room temperature.

[0043] Figure 8A is a graph of PFU / 100 μl of influenza A exposed to 15 wt% Si3N4 for 1, 5, 10, or 30 minutes at 4° C. Figure 8B is a graph of cell viability of influenza A inoculated cells exposed to 15 wt% Si3N4 for 1, 5, 10, or 30 minutes at 4° C.

[0044] Example 3: Effect of Silicon Nitride on H1H1 Influenza A Inactivation To demonstrate the effect of silicon nitride on viral inactivation, influenza A was exposed to a 15 wt % silicon nitride slurry for 10 minutes.

[0045] Figures 15A-C show H1H1 influenza A virus (A / Puerto Rico / 8 / 1934 H1N1 (PR8)) stained red after inoculation into biological medium containing MDCK cells stained green for the presence of filamentous actin (F-actin) protein found in all eukaryotic cells, and Figures 16A-C show the effect of the virus on MDCK cells in the absence of silicon nitride.

[0046] Example 4: Effect of silicon nitride on Plasmopara viticola To demonstrate the effect of silicon nitride on the inactivation of agricultural fungi, Cabernet Sauvignon leaves were infected with Plasmopara viticola at a concentration of 3 × 104 sporangia / mL. Treated Plasmopara viticola were exposed to a 1.5% by volume slurry of silicon nitride for 1 min.

[0047] FIG. 17(a) shows untreated Plasmopara viticola fungus on Cabernet Sauvignon leaves. FIG. 17(b) shows treated Plasmopara viticola fungus on Cabernet Sauvignon leaves. It can be seen that the leaves inoculated with Plasmopara viticola treated with 1.5% by volume of Si3N4 powder for 1 minute have less fungus on the leaf surface. This is further evidenced by FIG. 19, which shows the percentage of infected leaf area of ​​both control and treated Plasmopara viticola inoculated Cabernet Sauvignon and Cannonau leaves. FIG. 19 clearly shows that statistical significance wins over the infected leaf area between the control and treated fungus.

[0048] As seen in Figure 18B, the silicon nitride particles appear to be electrically attracted to and attach themselves to the pathogen spores. Figure 18A shows a microscopic image of an untreated sporangium of Plasmopara viticola, and Figure 18B shows a microscopic image of a sporangium of Plasmopara viticola in the presence of Si3N4.

[0049] Although several embodiments have been described, it will be recognized by those skilled in the art that various modifications, alternative configurations, and equivalents may be used without departing from the spirit of the present invention. In addition, some well-known processes and elements have not been described in order to avoid unnecessarily obscuring the present invention. Therefore, the above description should not be considered as limiting the scope of the present invention.

[0050] Those skilled in the art will understand that the embodiments of the present disclosure are taught by way of example and not by way of limitation. Therefore, the matter contained in the above description or shown in the accompanying drawings should be interpreted as illustrative and not limiting. The following claims are intended to cover, and may be considered as being linguistically contained therein, all the general and specific features described herein, as well as all the descriptions of the scope of the present methods and systems. Aspects of the invention include the following. <1> 1. A method for inactivating a pathogen, comprising: A method comprising contacting a device comprising silicon nitride with said pathogen, wherein said silicon nitride is present in or on said device at a concentration of about 1% to about 100% by weight. <2> further comprising coating the device with silicon nitride powder on the surface of the device. <1> The method according to <3> further comprising incorporating silicon nitride powder into the apparatus. <1> The method according to <4> contacting the device with a human patient at a location within the patient, wherein the pathogen is treated or prevented at the location. <1> The method according to <5> The device is in contact with the pathogen for at least 1 minute. <4> The method according to <6> the device is permanently implanted in the patient; <4> The method according to <7> the silicon nitride inactivates the pathogen; <1> The method according to <8> The pathogen comprises influenza A. <7> The method according to <9> 1. A method of treating or preventing a pathogen at a location in a human patient, comprising: <1> 20. A method comprising inactivating the pathogen described in claim 19. <10> 1. A method for inactivating a pathogen, comprising: A method comprising contacting the pathogen with a composition comprising silicon nitride at a concentration of about 1% to about 30% by volume. <11> the composition comprises a slurry of silicon nitride particles and water; <12> The method according to <12> further comprising spraying the composition onto a surface of a plant to contact the pathogen. <13> The method according to <13> The pathogen is treated or prevented at a location within the plant. <14> The method according to <14> the silicon nitride inactivates the pathogen; <12> The method according to <15> The pathogen comprises Plasmopara viticola. <16> The method according to <16> The plant comprises Cabernet Sauvignon or Cannonau. <17> The method according to <17> The composition is in contact with the pathogen for at least 1 minute. <12> The method according to <18> 1. A method for treating or preventing a pathogen at a location within a plant, comprising: <10> 20. A method comprising inactivating the pathogen described in claim 19.

Claims

1. A method for inactivating a plant pathogen, comprising the steps of: contacting said plant pathogens with a composition comprising a slurry of micrometer-sized silicon nitride particles and water at a concentration of 1% to 30% by volume; The plant pathogen comprises Plasmopara viticola; The method.

2. 10. The method of claim 1, further comprising spraying the composition onto a surface of a plant to contact the plant pathogen.

3. The method of claim 2 , wherein the plant pathogen is treated or prevented at a location within the plant.

4. The method of claim 1 , wherein the silicon nitride inactivates the plant pathogen.

5. The method of claim 1 , wherein the plant comprises Cabane Sauvignon or Cannonau.

6. The method of claim 1 , wherein the composition is contacted with the plant pathogen for at least 1 minute.

7. A method for treating or preventing a plant pathogen at a location within a plant, the method comprising inactivating the plant pathogen by the method of claim 1.

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