Antipathogenic nanostructures
US-2024341310-A1 · Oct 17, 2024 · US
US9277749B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9277749-B2 |
| Application number | US-201514615552-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 6, 2015 |
| Priority date | Feb 7, 2014 |
| Publication date | Mar 8, 2016 |
| Grant date | Mar 8, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Compositions and methods for the disinfection of surfaces are provided. The compositions include at least about 40 weight percent of a C 1-6 alcohol, and a primary enhancer selected from protein denaturants. The disinfectant composition is characterized by a pH of less than about 3. Broad spectrum efficacy is achieved, and synergistic activity is exhibited against C. difficile spores.
Opening claim text (preview).
What is claimed is: 1. A method for inactivation of C. difficile spores, the method comprising: contacting the spores with an disinfectant composition comprising: at least about 40 wt. % of a C 1-6 alcohol, and a primary enhancer selected from the group consisting of protein denaturants, wherein the disinfectant composition is characterized by a pH of less than about 3. 2. The method of claim 1 , wherein the disinfectant composition comprises at least about 50 wt. % of the C 1-6 alcohol, based upon the total weight of the disinfectant composition. 3. The method of claim 1 , wherein the primary enhancer is selected from the group consisting of amine-containing enhancers, α-aminoacids, salts of alkali metals, salts of alkaline earth metals, and anionic surfactants. 4. The method of claim 1 , wherein the amine-containing enhancer is selected from the group consisting of urea, dimethyl urea, thiourea, guanidine-HCl, guanidine thiocyanate, aminoguanidine bicarbonate, guanidine carbonate, guanidine phosphate, aminoguanidine-HCL, and mixtures thereof. 5. The method of claim 1 , wherein the primary enhancer is selected from the group consisting of sulfur-containing aminoacids and nitro-containing aminoacids. 6. The method of claim 1 , wherein the primary enhancer is selected from the group consisting of magnesium chloride, lithium perchlorate, and lithium acetate. 7. The method of claim 1 , wherein the primary enhancer is selected from the group consisting of anionic surfactants. 8. The method of claim 1 , wherein the enhancer is present in an amount of from about 0.1 to about 20 wt. %, based upon the total weight of the disinfectant composition. 9. The method of claim 1 , wherein the pH of the composition is less than about 2.75. 10. The method of claim 1 , wherein the composition further comprises a secondary enhancer selected from the group consisting of non-ionic surfactants, auxiliary antimicrobial agents, organic acids, and oxidizing agents. 11. A composition for the disinfection of surfaces, the composition comprising: at least about 40 wt. % of a C 1-6 alcohol, based upon the total weight of the composition, and a primary enhancer selected from the group consisting of protein denaturants, wherein the disinfectant composition is characterized by a pH of less than about 3, and wherein the composition exhibits a synergistically enhanced efficacy against bacterial and fungal spores, when compared to the efficacy of the alcohol or primary enhancer alone. 12. The composition of claim 11 , wherein the composition exhibits a synergistically enhanced efficacy against C. difficile spores, when compared to the efficacy of the alcohol or primary enhancer alone. 13. The composition of claim 11 , wherein the primary enhancer is selected from the group consisting of amine-containing enhancers, α-aminoacids, salts of alkali metals, salts of alkaline earth metals, and anionic surfactants. 14. The composition of claim 11 , wherein the amine-containing enhancer is selected from the group consisting of urea, thiourea, guanidine-HCl, guanidine thiocyanate, aminoguanidine bicarbonate, guanidine carbonate, guanidine phosphate, aminoguanidine-HCL, and mixtures thereof. 15. The composition of claim 11 , wherein the composition further comprises a secondary enhancer selected from the group consisting of non-ionic surfactants, auxiliary antimicrobial agents, organic acids, and oxidizing agents. 16. The composition of claim 11 , wherein the composition further comprises a secondary enhancer selected from the group consisting of decyl glucoside and polyalkoxylated dimethicones. 17. The composition of claim 11 , wherein the composition further comprises a secondary enhancer selected from the group consisting of citric acid, lauric acid, and tannic acid. 18. The composition of claim 11 , wherein the composition further comprises at least one auxiliary antimicrobial agent. 19. The composition of claim 11 , wherein the composition further comprises sodium nitrite.
Guanidine; Derivatives thereof · CPC title
Acyclic compounds · CPC title
Saturated carboxylic acids or thio analogues thereof; Derivatives thereof · CPC title
Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions · CPC title
Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.