IP Library Granted Patent US 9,820,482
Granted Patent B2
US 9,820,482 · App. 15/009,004 · Granted Nov 21, 2017

Compositions and methods with efficacy against spores and other organisms

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Quick Facts
Patent No.
US 9,820,482
App. No.
15/009,004
Granted
Nov 21, 2017
Kind
B2
Abstract

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.

Claims (16)

1. 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,

at least one primary enhancer, and

optionally, at least one secondary enhancer selected from the group consisting of non-ionic surfactants, organic acids, antimicrobial agents, oxidizing agents, sugars, sugar alcohols, monosaccharides, glycerol and combinations thereof,

wherein the disinfectant composition is characterized by a pH of less than about 3.

2. The composition of claim 1 , 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.

3. The composition of claim 1 , wherein the composition exhibits a synergistically enhanced efficacy against C. difficile spores, when compared to the efficacy of the alcohol or primary enhancer alone.

4. The composition 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, anionic surfactants, and combinations thereof.

5. The composition of claim 4 , 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 combinations thereof.

6. The composition of claim 1 , wherein the composition comprises at least two secondary enhancers.

7. The composition of claim 1 , wherein the at least one secondary enhancer is selected from the group consisting of decyl glucoside, polyalkoxylated dimethicones, glycerol, and combinations thereof.

8. The composition of claim 1 , wherein the organic acid is selected from the group consisting of citric acid, lauric acid, tannic acid, and combinations thereof.

9. The composition of claim 1 , wherein the antimicrobial agent is selected from the group consisting of triclosan, PCMX, chloroxylenol, hexetidine, chlorhexidine salts 2-bromo-2-nitropropane-1, 3-diol, benzalkonium chloride, cetylpyridinium chloride, alkylbenzyldimethylammonium chlorides, iodine, phenol, bisphenol, diphenyl ether, phenol derivatives, povidone-iodine, parabens, hydantoins and derivatives thereof, phenoxyethanol, cis isomer of 1-(3-chloroallyl)-3,5,6-triaza-1-azoniaadamantane chloride, diazolidinyl urea, benzethonium chloride, methylbenzethonium chloride, glyceryl laurate, transition metal compounds, hydrogen peroxide, chlorine dioxide, anilides, bisguanidines, tropolone, C 6-10 -alkane diols, and combinations thereof.

10. The composition of claim 1 , wherein the composition provides a log reduction against spores of at least I when the contact time is from about 30 seconds to about 5 minutes.

11. The composition of claim 1 , wherein the primary enhancer includes one or more salts selected from the group consisting of ammonium, calcium, iron, lithium, magnesium, and sodium salts.

12. The composition of claim 11 , wherein the primary enhancer is selected from the group consisting of ammonium chloride, ammonium iron citrate, calcium chloride, iron perchlorate, lithium perchlorate, lithium acetate, magnesium chloride, sodium chlorate, sodium chloride, sodium chlorite, 2-amino-2-hydroxy methyl-propane-1,3-diol hydrochloride, and combinations thereof.

Assignments (6)
RELEASE OF SECURITY INTEREST IN PATENT COLLATERAL, RECORDED ON OCTOBER 27, 2023 AT REEL 065382 FRAME 0587 Recorded Apr 22, 2026
From: SILVER POINT FINANCE, LLC, AS COLLATERAL AGENT
To: GOJO INDUSTRIES, INC.
Reel/Frame 075435/0852 →
RELEASE OF SECURITY INTEREST Recorded Apr 7, 2026
From: PNC BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: GOJO INDUSTRIES, INC.
Reel/Frame 074903/0480 →
SECURITY INTEREST Recorded Oct 27, 2023
From: GOJO INDUSTRIES, INC.
To: SILVER POINT FINANCE, LLC, AS COLLATERAL AGENT
Reel/Frame 065382/0587 →
SECURITY INTEREST Recorded Oct 26, 2023
From: GOJO INDUSTRIES, INC.
To: PNC BANK, NATIONAL ASSOCIATION
Reel/Frame 065369/0253 →
SECURITY INTEREST Recorded Dec 9, 2019
From: GOJO INDUSTRIES, INC.
To: PNC BANK, NATIONAL ASSOCIATION
Reel/Frame 051228/0667 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2017
From: BINGHAM, JAMES EDMUND; MACINGA, DAVID R.
To: GOJO INDUSTRIES, INC.
Reel/Frame 042852/0015 →