USE OF ETHOXYLATED ALCOHOLS TO IMPEDE ENVELOPED VIRAL SPREAD

Abstract

A method is provided in which a combination of an ethoxylated alcohol and an antimicrobial agent is used to impede virus spread. The method is particularly suitable to impede enveloped virus spread.

Claims

1. A method of impeding virus spread, the method comprising: using a combination of an ethoxylated alcohol and an antimicrobial agent to impede virus spread.

2. The method according to claim 1, wherein the virus is an enveloped virus.

3. The method according to claim 1, wherein the antimicrobial agent is selected from the group consisting of zinc pyrithione, quaternary ammonium silane, and a combination thereof.

4. The method according to claim 1, wherein the antimicrobial agent is selected from the group consisting of a silver compound, a copper compound, a quaternary ammonium compound or a mixture of quaternary ammonium compounds, and a combination thereof.

5. The method according to claim 1, wherein the antimicrobial agent is an organic acid.

6. The method according to claim 1, wherein the combination is applied to a substrate.

7. The method according to claim 6, wherein the substrate is a porous or non-porous surface.

8. The method according to claim 6, wherein the substrate is a textile.

9. The method according to claim 1, wherein the combination is incorporated into a polymer or a paper.

10. A method of using an ethoxylated alcohol, the method comprising: applying an ethoxylated alcohol and an antimicrobial agent to a substrate to impede virus spread.

11. The method according to claim 10, wherein the antimicrobial agent is selected from the group consisting of zinc pyrithione, quaternary ammonium silane, and a combination thereof.

12. The method according to claim 10, wherein the antimicrobial agent is selected from the group consisting of a silver compound, a copper compound, a quaternary ammonium compound or a mixture of quaternary ammonium compounds, and a combination thereof.

13. The method according to claim 10, wherein the antimicrobial agent is an organic acid.

14. The method according to claim 10, wherein the substrate is a porous or non-porous surface.

15. The method according to claim 10, wherein the substrate is a textile.

16. A method of using an ethoxylated alcohol, the method comprising: incorporating an ethoxylated alcohol and an antimicrobial agent into a polymer or a paper to impede virus spread.

17. The method according to claim 16, wherein the virus is an enveloped virus.

18. A method of using an ethoxylated alcohol, the method comprising: using an ethoxylated alcohol in combination with an antimicrobial agent to achieve an efficacy with less antimicrobial agent than is needed to achieve the efficacy with antimicrobial agent alone.

19. A composition comprising: an ethoxylated alcohol, and an antimicrobial agent, wherein the composition has an antiviral effect.

20. The composition according to claim 19, wherein the antimicrobial agent is selected from the group consisting of zinc pyrithione, quaternary ammonium silane, and a combination thereof.

Description

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0017] The following description of the embodiments of the present invention is merely exemplary in nature and is in no way intended to limit the invention, its application, or uses. The following description is provided herein solely by way of example for purposes of providing an enabling disclosure of the invention, but does not limit the scope or substance of the invention.

[0018] In accordance with the present invention, a method for impeding an enveloped viral spread is provided. The method comprises use of an ethoxylated alcohol, more preferably use of an ethoxylated alcohol in combination with an antimicrobial agent.

[0019] In an embodiment of the invention, the antimicrobial agent is selected from the group consisting of zinc pyrithione, quaternary ammonium silane, and a combination thereof.

[0020] In an embodiment of the invention, the antimicrobial agent is selected from the group consisting of a silver compound, a copper compound, a quaternary ammonium compound or a mixture of quaternary ammonium compounds, and a combination thereof.

[0021] In an embodiment of the invention, the antimicrobial agent is an organic acid.

[0022] Structurally, ethoxylated alcohols have a hydrophilic head group that is characterized by a repeating unit of an ethoxy component and a lipophilic tail group that is characterized by a linear carbon chain. The head group can be altered by altering the degree or moles of ethoxylation, from 1 to 16. The tail group typically has varying chain lengths from C4-C16.

[0023] In accordance with the method of the present invention, an ethoxylated alcohol(s) is combined with an antimicrobial agent to accentuate the activity of the antimicrobial agent against enveloped viruses by increasing the fluidity of the envelope layer. When the permeability of the envelope layer is altered, the penetrability and antiviral properties of the antimicrobial agent are believed to be amplified without a concurrent increase in antimicrobial concentration. The inclusion of the ethoxylated alcohol(s) allows a concomitant decrease in the amount of antimicrobial needed to achieve a similar benefit.

[0024] In the method of the present invention, the ethoxylated alcohol is used to accentuate the antiviral properties of an antimicrobial agent. This accentuation occurs across multiple classes of antimicrobial agents. Additionally, the carbon chain length and degree of ethoxylation may alter the observed accentuation benefit. Preferably, when the number of carbons is ≥9 carbons, the degree of ethoxylation is >5 moles of ethoxylation.

[0025] Additionally, the combination of the ethoxylated alcohol and the antimicrobial agent can be paired with other adjuvants depending on the end use scenario. For example, compatibilizers may be used to incorporate the ethoxylated alcohol into a polymer. Adjuvants for cleaning performance, streaking, shine, stability, and compatibility can be added for any of the below descriptions to allow for ease of use by the end consumer.

Example 1. Multiple Chemistries with Ethoxylated Alcohols on Textiles

[0026] Two different antimicrobials were studied: zinc pyrithione and quaternary ammonium silane. Each chemistry was tested separately and in combination with the selected ethoxylated alcohol. The chemistries (with and without the ethoxylated alcohol) were pad-applied to a representative textile material and tested per ISO 18184 specification using an enveloped bacteriophage Phi6 (a much-studied surrogate of enveloped human viruses). A pass requirement in the ISO 18184 is a 2 log reduction (99% reduction). Table 1 shows that the antimicrobial agents have limited antiviral activity at the stated concentrations. However, addition of an ethoxylated alcohol increased the permeability of the envelope layer, thereby allowing access of the antimicrobial agent to the remainder of the virion. This accentuated the activity of the antimicrobial by increasing the log reduction from <1 log reduction to >3 log reduction when compared to the untreated controls. Thus, there was an unexpected and synergistic effect achieved with the combination of an ethoxylated alcohol and an antimicrobial agent. Results are shown in Table 1.

TABLE-US-00001 TABLE 1 The Antiviral Performance of Zinc Pyrithione When Applied With or Without Ethoxylated Alcohol to Textiles Sample Viable Log # Sample description organisms reduction Inoculum [Plate Count (Phi6 stock S 2000000 diluted in Butterfield's Buffer without additional soil) 2 hour contact time.] 1 Textile with 0.336% Zinc pyrithione <20 4.8 and 0.5% Ethoxy alcohol, replicate 1 2 Textile with 0.336% Zinc pyrithione 500 3.4 and 0.5% Ethoxy alcohol, replicate 2 3 Textile with 0.336% Zinc pyrithione 900 3.2 and 0.5% Ethoxy alcohol, replicate 3 4 Textile with 0.336% Zinc pyrithione, 720000 0.3 replicate 1 5 Textile with 0.336% Zinc pyrithione, 130000 1.0 replicate 2 6 Textile with 0.336% Zinc pyrithione, 184000 0.9 replicate 3 7 Textile control, replicate 1 1500000 8 Textile control, replicate 2 1340000 9 Textile control, replicate 3 1260000 Mean of untreated control for 1363082 reduction calculation

TABLE-US-00002 TABLE 2 The Antiviral Performance of Quaternary Ammonium Silane When Applied With or Without Ethoxylated Alcohol to Textiles Sample Viable Log # Sample description organisms reduction Inoculum [Plate Count (Phi6 stock S 2560000 diluted in Butterfield's Buffer without additional soil) 2 hour contact time.] 1 Textile with 0.972% Quaternary 200 4.4 Ammonium Silane and 0.5% Ethoxy alcohol, replicate 1 2 Textile with 0.972% Quaternary <200 4.4 Ammonium Silane and 0.5% Ethoxy alcohol, replicate 2 3 Textile with 0.972% Quaternary <200 4.4 Ammonium Silane and 0.5% Ethoxy alcohol, replicate 3 4 Textile with 0.972% Quaternary 2020000 0.4 Ammonium Silane, replicate 1 5 Textile with 0.972% Quaternary 5840000 −0.1 Ammonium Silane, replicate 2 6 Textile with 0.972% Quaternary 2560000 0.3 Ammonium Silane, replicate 3 7 Textile control, replicate 1 6000000 8 Textile control, replicate 2 3820000 9 Textile control, replicate 3 4620000 Mean of untreated control for 4730992 reduction calculation

Example 2. Different Carbon Chain Lengths and Degree of Ethoxylation (EO)

[0027] For use as a liquid, only one antimicrobial was selected for evaluation. The material was formulated into a spray product with quaternary silane as the base antimicrobial. Two different ethoxylated alcohols were utilized. One had a 9-carbon chain length with 5 EO and the other was a mixture of compounds with a range of carbon chain lengths from C12-C14 and 12 EO. These were tested per a modified EPA 01-1A where a “pass” criterion is set at a minimum of 99.9% reduction (3 log reduction). In summary, the antimicrobial formulation was applied to a glass substrate and allowed to dry. Once dry, the durability of the film was tested by exposing it to wet and dry abrasions (that simulate cleaning actions) with a Gardco wear tester. The film was then inoculated with a known concentration of enveloped virus (Phi6) and assessed for the surviving viral particles against the untreated controls to measure antiviral activity. Table 2 below shows that the short carbon chain ethoxylated alcohol (C9, 5EO) did not provide sufficient permeabilization of the envelope to allow quaternary silane to act upon the virion, resulting in a failing result (no efficacy). The combination of the quaternary silane with the longer carbon chain ethoxylated alcohol (C12-15, 12EO) provided passing results (≥99.9% reduction).

TABLE-US-00003 TABLE 3 The Effect of Carbon Chain Length and Degree of Ethoxylation on Antiviral Efficacy of An Antimicrobial Mean viable % Sample description organisms Reduction Control 37641 Quaternary Ammonium Silane with 3032 91.95 Fail C9, 5EO Control 123623 Quaternary Ammonium Silane with <10 99.99 Pass C12-15, 12EO

[0028] The specific combination of the ethoxylated alcohol can be used to accentuate the antiviral efficacy of existing antimicrobials. The ethoxylated alcohol in combination with an antimicrobial can be utilized as a spray, concentrate, foam, fogging, wipe, or alternate format. The ethoxylated alcohol in combination with an antimicrobial can be applied to a textile via a spray, pad bath, exhaust bath, kiss roller, or embossing. The ethoxylated alcohol combination with an antimicrobial can be incorporated into paper via a masterbatch during milling or during finishing as described for the textile. The ethoxylated alcohol in combination with an antimicrobial can be incorporated into a polymer in a masterbatch or end use concentration.

[0029] The specific combination of the ethoxylated alcohol can be used to accentuate the antiviral efficacy of existing antimicrobials.

[0030] Present technologies only allow for immediate disinfection of the virus. Immediately following a touch, cough, sneeze, or settling of an aerosolization droplet the surface is re-contaminated. Viruses with high infectivity rates can survive on surfaces for days (Kramer et al, 2006). The combination and method of the present invention can provide continual antiviral protection on exposed surfaces in multiple formats. It can be incorporated into a solid surface, such as a textile or polymer, allowing surface protection. Additionally, it can be combined in a liquid based product for post-manufacture application.

[0031] Thus, in the present invention, ethoxylated alcohol is paired with an antimicrobial agent to enhance associated antiviral activity. Additionally, the antimicrobial and ethoxylated alcohol combination described herein shifts the parabolic distribution need of the degree of ethoxylation such as to 12 mol of ethoxylate.

Example 3

[0032] A textile formulation was tested on polyester. The C12-15 and 12 mol ethoxylate was added ranging from 0.05 weight % to 0.5 weight % on weight of good. The material was pad-applied to the textile and then cured at 150° C. for 45 seconds. The material was tested for durability using 2 cycles of the AATCC 61(2A) protocol. As made, the material was able to reduce 99.9% (3 log reduction) of an enveloped bacteriophage (Phi6). Upon washing with 2 cycles of the 61(2A) protocol, the efficacy was still apparent but was reduced to 90% (1 log reduction) reduction of the Phi6 bacteriophage.

[0033] Additionally, a spray formula was tested for efficacy and durability against Phi6 (see example 2 above).

[0034] It will therefore be readily understood by those persons skilled in the art that the present invention is susceptible of broad utility and application. Many embodiments and adaptations of the present invention other than those herein described, as well as many variations, modifications and equivalent arrangements, will be apparent from or reasonably suggested by the present invention and the foregoing description thereof, without departing from the substance or scope of the present invention. Accordingly, while the present invention has been described herein in detail in relation to its preferred embodiment, it is to be understood that this disclosure is only illustrative and exemplary of the present invention and is made merely for purposes of providing a full and enabling disclosure of the invention. The foregoing disclosure is not intended or to be construed to limit the present invention or otherwise to exclude any such other embodiments, adaptations, variations, modifications and equivalent arrangements.