IP Library Patent Application 12090938
Patent Application
App. No. 12/090,938

Antimicrobial Composition and Method

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Patent No.
US None
App. No.
12/090,938
Abstract

An antimicrobial composition containing a cationic polymer having limited antimicrobial activity (such as a hydrophobically-modified quaternary ammonium cellulose ether) and an antimicrobial compound (such as one or more compounds selected from the group consisting of diiodomethyl-para-tolylsulfone, ortho-phenylphenol, sodium pyrithione, zinc pyrithione, 3-iodo-2-propynylbutylcarbamate, 2-methyl-4-isothiazolin-3-one, 1,2-benzisothiazolin-3-one, 2-n-octyl-4-isothiazolin-3-one, 1-(3-chloroallyl)-3,5,7-triaza-1-azoniaadamantane chloride, 2-(4-thiazolyl)-benzimidazole, β-bromo-β-nitrostyrene, 2,4,4′-trichloro-2-hydroxyphenyl ether, chloroxylenol, chlorocresol, para-tert-amylphenol, N-(4-chlorophenyl)-N′-(3,4 dichlorophenyl)-urea, and para-hydroxybenzoic acid esters). The growth of microorganisms (such as Pseudomonas aeruginosa ) can be inhibited by exposing the microorganism to such a composition.

Claims (18)

1 . An antimicrobial composition, comprising: a cationic polymer having limited antimicrobial activity; and an antimicrobial compound.

2 . The composition of claim 1 , wherein the antimicrobial compound comprises one or more compounds selected from the group consisting of diiodomethyl-para-tolylsulfone, ortho-phenylphenol, sodium pyrithione, zinc pyrithione, 3-iodo-2-propynylbutylcarbamate, 2-methyl-4-isothiazolin-3-one, 1,2-benzisothiazolin-3-one, 2-n-octyl-4-isothiazolin-3-one, 1-(3-chloroallyl)-3,5,7-triaza-1-azoniaadamantane chloride, 2-(4-thiazolyl)-benzimidazole, β-bromo-β-nitrostyrene, 2,4,4′-trichloro-2-hydroxyphenyl ether, chloroxylenol, chlorocresol, para-tert-amylphenol, N-(4-chlorophenyl)-N′-(3,4-dichlorophenyl)-urea, and para-hydroxybenzoic acid esters.

3 . The composition of claim 1 , wherein the antimicrobial compound has a solubility in water of about 0.5 weight percent or less.

4 . The composition of claim 1 , wherein the cationic polymer is a cationic polysaccharide.

5 . The composition of claim 1 , wherein the cationic polymer is a hydrophobically-modified cationic polysaccharide.

6 . The composition of claim 5 , wherein the hydrophobically-modified cationic polysaccharide is a hydrophobically-modified cationic cellulose ether.

7 . The composition according to claim 1 , wherein the antimicrobial compound comprises one or more compounds selected from the group consisting of DIMTS, OPP, NaPT, ZPT, IPBC, BIT, OIT, TBZ, BNS, 2,4,4′-trichloro-2-hydroxyphenyl ether, chloroxylenol, chlorocresol, PTAP, and N-(4-chlorophenyl)-N′-(3,4-dichlorophenyl)-urea.

8 . The composition of claim 1 , further comprising one or more of a surfactant, a pH modifiers; a salts; a rheology modifier; a dispersion stabilizers; a chelant; a fragrance; a pigments; a dye, and a UV-active compound.

9 . A method of inhibiting the growth of a microorganism by the step of exposing the microorganism to the composition of claim 1 .

10 . The method of claim 9 , wherein the microorganism is Pseudomonas aeruginosa.

11 . A bactericidal soap composition comprising:

a fatty acid soap; and

an antimicrobial composition according to claim 1 .

12 . The bactericidal soap composition of claim 11 comprising between about 45 weight percent and about 95 weight percent of the fatty acid soap.

13 . The bactericidal soap composition of claim 11 wherein the weight ratio of cationic polymer to antimicrobial compound is between about 200:1 and 1:1.

14 . The bactericidal soap composition of claim 11 wherein the antimicrobial compound is 2,4,4′-trichloro-2-hydroxyphenyl ether, chloroxylenol, chlorocresol, para-tert-amylphenol, N-(4-chlorophenyl)-N′-(3,4-dichlorophenyl)-urea, or mixtures thereof.

15 . The bactericidal soap composition of claim 11 wherein the cationic polymer is a cationic polysaccharide or a hydrophobically-modified cationic polysaccharide.

16 . The bactericidal soap composition of claim 11 wherein the cationic polymer comprises a hydrophobically-modified cationic polysaccharide.

Assignments (2)
CHANGE OF NAME Recorded Mar 17, 2011
From: DOW GLOBAL TECHNOLOGIES INC.
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 025979/0946 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2008
From: ANNIS, IOANA; GARTNER, CHARLES D.
To: DOW GLOBAL TECHNOLOGIES INC.
Reel/Frame 021146/0387 →