HYDROPHOBIC SURFACE COATING FOR VIRUS INACTIVATION AND METHODS THEREFOR
20220235246 · 2022-07-28
Inventors
- Tanya Purwar (Lafayette, IN, US)
- Victor-Manuel Castano-Meneses (Queretaro, MX)
- Xing Li (West Lafayette, IN, US)
- Ernest R. Blatchley, III (Lafayette, IN, US)
- Luciano Castillo (Carmel, IN, US)
- Ali Doottalab (Lubbock, TX, US)
Cpc classification
B05D1/04
PERFORMING OPERATIONS; TRANSPORTING
B05D5/08
PERFORMING OPERATIONS; TRANSPORTING
International classification
B05D1/04
PERFORMING OPERATIONS; TRANSPORTING
B05D5/08
PERFORMING OPERATIONS; TRANSPORTING
Abstract
Methods of enhancing the anti-virus capabilities of surfaces directly contacted by humans. The methods include applying a hydrophobic coating material to a surface of an article to form a hydrophobic surface coating overlying the surface such that the hydrophobic surface coating defines a hydrophobic outer surface of the article. The hydrophobic outer surface is more hydrophobic than the surface of the article, and a liquid that contains suspended viruses and is deposited on the hydrophobic outer surface exhibits a contact angle relative to the hydrophobic outer surface that is greater than a contact angle of the liquid if directly deposited on the surface of the article, and the hydrophobic outer surface thereby increases inactivation of the viruses suspended in the liquid as compared to the surface of the article to which the hydrophobic coating material was applied.
Claims
1. A method of increasing inactivation of viruses that come into contact with an article that is directly contacted by humans when the article is handled by humans, the method comprising: applying a hydrophobic coating material to a surface of the article to form a hydrophobic surface coating overlying the surface, the hydrophobic surface coating defining a hydrophobic outer surface of the article that is directly contacted by humans when the article is handled by humans, the hydrophobic outer surface being more hydrophobic than the surface of the article to which the hydrophobic coating material was applied; and depositing on the hydrophobic outer surface a liquid in which viruses are suspended, the liquid exhibiting a contact angle relative to the hydrophobic outer surface that is greater than a contact angle of the liquid relative to the surface of the article to which the hydrophobic coating material was applied if the liquid were directly deposited on the surface of the article without the hydrophobic surface coating and the hydrophobic outer surface thereby increasing inactivation of the viruses suspended in the liquid as compared to the surface of the article to which the hydrophobic coating material was applied.
2. The method according to claim 1, wherein the hydrophobic surface coating is continuous and uninterrupted.
3. The method according to claim 1, wherein the liquid is saliva or nasal fluid.
4. The method according to claim 1, wherein the liquid is deposited on the hydrophobic outer surface as one or more droplets.
5. The method according to claim 1, wherein the contact angle of the liquid relative to the surface of the article is less than 90 degrees and the contact angle of the liquid relative to the hydrophobic outer surface is greater than 90 degrees.
6. The method according to claim 1, wherein the contact angle of the liquid relative to the surface of the article is less than 100 degrees and the contact angle of the liquid relative to the hydrophobic outer surface is greater than 100 degrees to about 130 degrees.
7. The method according to claim 1, wherein the contact angle of the liquid relative to the hydrophobic outer surface is at least 36% greater than the contact angle of the liquid relative to the surface of the article.
8. The method according to claim 1, wherein the contact angle of the liquid relative to the hydrophobic outer surface is at least 50% greater than the contact angle of the liquid relative to the surface of the article.
9. The method according to claim 1, wherein the hydrophobic coating material is a silicone-based material, polydimethylsiloxane, or a fluoropolymer.
10. The method according to claim 1, wherein the hydrophobic coating material is lipophobic.
11. The method according to claim 1, wherein the hydrophobic coating material is applied by electrostatic spraying.
12. The method according to claim 1, wherein the article is a high-touch object in a medical facility.
13. The method according to claim 1, wherein the surface of the article is formed by a material chosen from the group consisting of wood, polymers, and metals.
14. The method according to claim 1, wherein the surface of the article is formed by a material chosen from the group consisting of wood, polytetrafluoroethylene, polypropylene, polyvinyl chloride, polyethylene, natural rubber, copper, aluminum, stainless steel, and cast iron.
Description
BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING
[0012]
[0013]
[0014]
[0015]
[0016]
[0017]
[0018]
[0019]
DETAILED DESCRIPTION OF THE INVENTION
[0020] The intended purpose of the following detailed description of the invention and the phraseology and terminology employed therein is to describe what is shown in the drawings, which relate to one or more nonlimiting embodiments of the invention, and to describe certain but not all aspects of what is depicted in the drawings, including the embodiment(s) to which the drawings relate. The following detailed description also describes certain investigations relating to the embodiment(s), and identifies certain but not all alternatives of the embodiment(s). Therefore, the appended claims, and not the detailed description, are intended to particularly point out subject matter regarded as the invention, including certain but not necessarily all of the aspects and alternatives described in the detailed description.
[0021] On the basis that viruses become inactivated and proteins lose activity upon exposure to air-water interfaces (AWI) and stronger inactivation is expected at the triple-phase-boundary (TPB) of a three-part system comprising an aqueous medium, a solid surface, and air, the following disclosure utilizes these properties to increase virus inactivation with the use of coatings that are strongly hydrophobic.
[0022] Experiments were conducted with surfaces having different wettabilities for the purpose of determining the effect on virus inactivation due to interfacial forces in a static triple-phase-boundary system. For the experiments, low wettability surfaces were formed with Rust-Oleum® 278146 Never-Wet Outdoor Fabric Spray, a silicone-based hydrophobic and lipophobic coating material having an ultra-low volatile organic compound (VOC) content and able to be applied by electrostatic spraying methods. This hydrophobic coating material was selected in part on the basis of being reported as superhydrophobic.
[0023] Specimen substrate materials used in the experiments included wood, polymer, and metals, in particular, wood, polytetrafluoroethylene (PTFE), polypropylene (PP), polyvinyl chloride (PVC), polyethylene (PE), natural rubber (mainly polyisoprene), copper, aluminum, stainless steel, and cast iron.
[0024] Viruses used in the experiments were Escherichia virus MS2 (MS2) and Pseudomonas virus phi6 (phi6) bacteriophages. MS2 is a nonenveloped, single stranded RNA, and Phi6 is an enveloped, double stranded RNA.
[0025] The experiments employed saliva as the liquid from which wettabilities of different surfaces were determined, though it should be understood that viruses can be and often are transferred or dispersed while suspended in other liquids. A notable but nonlimiting example is nasal fluid, which deposits on articles and is dispersed in the air as a result of sneezing.
[0026] The following test techniques were performed. Specimen substrates of the different specimen substrate materials were obtained. Surfaces of some of the specimen substrates were coated with the hydrophobic coating material, while the remaining specimen substrates remained uncoated. Using pipettes, a liquid (saliva) droplet was suspended on each coated and uncoated specimen substrate, and contact angles of the droplets were measured using a sessile drop test. As used herein, the term “contact angle(s)” refers to the contact angle of a liquid droplet relative to a surface of a solid on which the droplet is supported. As schematically represented in
[0027]
[0028] Virus inactivation of phi6 bacteriophages was investigated with aluminum and polypropylene as specimen substrate materials. One of each specimen substrate material was coated with the hydrophobic coating material, and one of each specimen substrate material remained uncoated. Four drops of a 7-microliter phi6 stock were applied with a pipette to each coated and uncoated specimen substrate. The droplets were allowed to rest on their surfaces for thirty minutes, after which a 10 mL broth was used to extract bacteriophages from each surface.
[0029] Phi6 inactivation was determined using a plaque assay test, which is a widely used approach for determining the quantity of infectious viruses in a sample. Only viruses that cause visible damage to cells can be assayed in this way. The number of plaques that develop and the appropriate dilution factors can be used to calculate the number of bacteriophages, i.e., plaque-forming units (PFU) in a sample.
[0030] Illustrative of the results discussed in reference to
[0031] The investigations discussed above evidenced that hydrophobicity (resulting in low wettability) of a surface contacted by a liquid containing suspended viruses was a crucial parameter in the cause of virus inactivation on surfaces. Consequently, it was concluded that a hydrophobic surface coating that is continuous and uninterrupted over a surface of a substrate will create a hydrophobic surface coating that increases virus inactivation as compared to the original surface of the substrate. In regard to articles handled by humans, surfaces of such articles that are frequently handled by humans are believed to particularly benefit as a result of increased inactivation of viruses that are deposited on the surfaces.
[0032] While the invention has been described in terms of particular investigations, it should be apparent that alternatives could be adopted by one skilled in the art. For example, other hydrophobic coating materials and substrate materials could be substituted for those used in the investigations. Notable examples of other hydrophobic coating materials include super hydrophobic and super lipophobic coating compositions that comprise polydimethylsiloxane and optionally may contain functionalized carbonaceous nanoparticles, and fluoropolymer coatings that optionally may contain functional groups. Accordingly, it should be understood that the invention is not necessarily limited to any particular embodiment or investigation described herein or illustrated in the drawings. It should also be understood that the purpose of the above detailed description and the phraseology and terminology employed therein is to describe the investigations, and not necessarily to serve as limitations to the scope of the invention. Therefore, the scope of the invention is to be limited only by the following claims.