IP Library Granted Patent US 7,094,394
Granted Patent B2
US 7,094,394 · App. 10/188,354 · Granted Aug 22, 2006

Methods and compositions for controlling biofilm development

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Quick Facts
Patent No.
US 7,094,394
App. No.
10/188,354
Granted
Aug 22, 2006
Kind
B2
Abstract

A method of cleaning or protecting surfaces by treatment with compositions comprising N-(3-oxododecanoyl)-L-homoserine lactone (OdDHL) blocking compounds and/or N-butyryl-L-homoserine lactone (BHL) analogs, either in combination or separately.

Claims (37)

1. A biofilm removing or inhibiting composition comprising an effective amount for regulating biofilm development of a compound selected from the group consisting of blockers of N-(3-oxododecanoyl) L-homoserine lactone (OdDHL), and analogs of butyryl L-homo-serine lactone (BHL), and mixtures thereof, and a vehicle or carrier, wherein the amount of the compound is effective to remove or disrupt a bacterial biofilm or inhibit normal biofilm formation, and wherein an effective amount for regulating biofilm development of blockers of N-(3-oxododecanoyl) L-homoserine lactone is between about 2.5 μM and 50 μM, and effective amount for regulating biofilm development of analogs of butyryl L-homoserine lactone is between about 5 μM and 100 μM.

2. The composition of claim 1 wherein the compound is an OdDHL blocker having the following structure:

wherein in the above formulae R 1 –R 21 are selected from the group consisting of H, C 1 –C 4 alkyl group, CU 3 , OH, NH 2 , SH, a halogen, fluorine, chlorine, bromine and iodine;

R 22 and R 23 are selected from S and O,

R 24 –R 28 is H or a halogen, and

X, X 1 and X 2 are selected from O, S, H 2 or any combination of H plus one halogen or two halogens when one or more R groups is substituted.

3. The composition in claim 1 wherein R 22 through R 28 is a H or halogen.

4. The composition in claim 2 wherein one or more carbons forming the backbone of the molecule are substituted with S or S-substituted moieties.

5. The composition of claim 2 wherein the carbonyl group at X 1 andlor X 2 is substituted with H 2 , H plus a halogen or two halogens.

6. The composition of claim 1 wherein the compound is a butyryl-L-homoserine lactone (BHL) analog having the following structure:

wherein in the above formulae R 1 –R 7 are selected from the group consisting of H, C 1 –C 4 alkyl group, CH 3 , OH, NH 2 , SH, a halogen, fluorine, chlorine, bromine and iodine;

R 22 and R 23 are selected from S and O,

R 24 –R 28 is H or a halogen, and

X, X 1 and X 2 are selected from O, S, H 2 or any combination of H plus one halogen or two halogens when one or more R groups is substituted.

7. The composition of claim 6 , wherein R 22 is selected from H, S, O and NH and R 23 is selected from S, O, and N.

8. The composition of claim 6 , wherein the acyl side chain contains one or more double bonds or triple bonds between carbon atoms within the acyl side chain.

9. The composition of claim 6 wherein X is selected from H 2 , H plus a halogen, two halogens, H plus OH or NH 2 , a double bonded O, NH or S.

10. The composition of claim 1 additionally comprising a surfactant selected from the group consisting of anionic, nonionic, amphoteric, biological surfactants and mixtures thereof.

11. The composition of claim 10 , wherein the surfactant is sodium dodecyl sulfate.

12. The composition of claim 2 in which the blocker is N-(2,2 difluorodecanoyl)-L-homoserine lactone.

13. The composition of claim 1 further comprising a compound selected from the group consisting of biocides, fungicides, antibiotics, and mixtures thereof.

14. A method of removing biofilm from a surface comprising the step of administering a cleaning-effective amount of the composition of claim 1 to a biofilm-containing surface.

15. A method of preventing biofilm formation on a surface comprising the step of administering an effective amount of the composition of claim 1 to a surface, wherein the amount is effective to prevent biofilm formation.

16. The method of claim 14 wherein the surface is a hard, rigid surface.

17. The method of claim 16 wherein the surface is selected from the group consisting of a drainpipe, glaze ceramic, porcelain, glass, metal, wood, chrome, plastic, vinyl, and formica.

18. The method of claim 14 wherein the surface is a soft, flexible surface.

19. The method of claim 18 wherein the surface is selected from the group consisting of shower curtains or liners, upholstery, laundry, and carpeting.

20. The method of claim 14 wherein the biofilm is produced by a bacteria of the class Pseudomonas.

21. The method of claim 20 wherein the bacteria is of the species Pseudomonas aeuroginosa.

22. The method of claim 14 wherein the biofilm is produced by an organism selected from the, group consisting of bacteria, algae, fungi and protozoa.

23. A dentifrice comprising an effective amount of a composition of claim 1 , wherein the amount is effective to either prevent or remove biofilm formation.

24. A mouthwash comprising an effective amount of a composition of claim 1 , wherein the amount is effective to either prevent or remove biofilm formation.

25. A method for treatment of dental caries comprising administering an effective amount of a composition of claim 1 , wherein the amount is effective to either prevent or remove biofilm formation.

26. A method of prevention of dental caries comprising administering an effective amount of a composition of claim 1 , wherein the amount is effective to either prevent or remove biofilm formation.

27. A method of treatment of acne comprising topically administering an effective amount of a composition of claim 1 , wherein the amount is effective to either prevent or remove biofilm formation.

28. A method of cleaning and disinfecting contact lenses comprising administering an effective amount of a composition of claim 1 , wherein the amount is effective to either prevent or remove biofilm formation.

29. A microbial dispersing composition comprising an effective amount of composition of claim 1 , wherein the amount is effective to either prevent or remove biofilm formation.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 19, 2002
From: RESEARCH AND DEVELOPMENT INSTITUTE, INC.
To: MONTANA STATE UNIVERSITY
Reel/Frame 013467/0060 →