IP Library Granted Patent US 7,619,008
Granted Patent B2
US 7,619,008 · App. 11/194,039 · Granted Nov 17, 2009

Xylitol for treatment of vaginal infections

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Quick Facts
Patent No.
US 7,619,008
App. No.
11/194,039
Granted
Nov 17, 2009
Kind
B2
Abstract

A vaginal treatment composition that employs a therapeutic agent to inhibit and/or treat vaginal infection is provided. The therapeutic agent is capable of inhibiting and/or killing Gardnerella (e.g., Gardnerella vaginalis ), Candida (e.g., Candida albicans ), and/or Trichomonas (e.g., Trichomonas vaginalis ) pathogens. Desirably, such antimicrobial efficacy is achieved without substantially inhibiting the growth of Lactobacillus acidophilus. For instance, sugars and/or sugar alcohols may be employed in the present invention as a therapeutic agent for inhibiting and/or treating vaginal infection. In one particular embodiment, D-xylitol is used as the therapeutic agent.

Claims (40)

1. A method for treating bacterial vaginosis caused by Gardnerella vaginalis , the method comprising topically administering to the vagina of a female in need thereof a vaginal treatment composition comprising:

from about 0.1 wt/vol % to about 10 wt/vol % of at least one therapeutic agent that includes xylitol, and

from about 0.05 wt/vol % to about 5 wt/vol % of at least one gelling agent that includes gellan gum,

wherein the vaginal treatment composition has an osmolarity of from about 270 to about 310 milliosmoles per liter and a pH of from about 2.5 to about 5.0, and

wherein the treatment composition forms a gel after application to the vagina.

2. The method of claim 1 , wherein the vaginal treatment composition comprises from about 0.2 wt/vol % to about 5.0 wt/vol % of xylitol.

3. The method of claim 1 , wherein the vaginal treatment composition comprises from about 0.5 wt/vol % to about 4.5 wt/vol % of xylitol.

4. The method of claim 1 , wherein the vaginal treatment composition has an osmolarity of from about 280 to about 300 milliosmoles per liter.

5. The method of claim 1 , wherein the vaginal treatment composition is substantially free of tonicity agents other than xylitol.

6. The method of claim 1 , wherein the therapeutic agent consists of xylitol.

7. The method of claim 1 , wherein the vaginal treatment composition has a pH of from about 3.0 to about 4.5.

8. The method of claim 1 , wherein the vaginal treatment composition further comprises a pH modifier.

9. The method of claim 8 , wherein the pH modifier is a carboxylic acid.

10. The method of claim 8 , wherein the pH modifier is lactic acid.

11. The method of claim 8 , wherein the pH modifier is gallic acid.

12. The method of claim 1 , wherein the gelling agent is present in the composition in an amount of from about 0.1 wt/vol % to about 1 wt/vol %.

13. The method of claim 1 , wherein the composition is substantially free of monovalent and divalent salts.

14. The method of claim 1 , wherein the gelling agent includes low acyl gellan gum.

15. The method of claim 1 , wherein the vaginal treatment composition inhibits the growth of Gardnerella vaginalis.

16. The method of claim 1 , wherein the vaginal treatment composition does not substantially inhibit the growth of Lactobacillus acidophilus.

17. A method for treating trichomonas vaginitis caused by Trichomonas vaginalis , the method comprising topically administering to the vagina of a female in need thereof a vaginal treatment composition comprising:

from about 0.1 wt/vol % to about 10 wt/vol % of at least one therapeutic agent that includes xylitol, and

from about 0.05 wt/vol % to about 5 wt/vol % of at least one gelling agent that includes gellan gum,

wherein the vaginal treatment composition has an osmolarity of from about 270 to about 310 milliosmoles per liter and a pH of from about 2.5 to about 5.0, and

wherein the treatment composition forms a gel after application to the vagina.

18. The method of claim 17 , wherein the vaginal treatment composition comprises from about 0.2 wt/vol % to about 5.0 wt/vol % of xylitol.

19. The method of claim 17 , wherein the vaginal treatment composition comprises from about 0.5 wt/vol % to about 4.5 wt/vol % of xylitol.

20. The method of claim 17 , wherein the vaginal treatment composition has an osmolarity of from about 280 to about 300 milliosmoles per liter.

21. The method of claim 17 , wherein the therapeutic agent consists of xylitol.

22. The method of claim 17 , wherein the vaginal treatment composition has a pH of from about 3.0 to about 4.5.

23. The method of claim 17 , wherein the vaginal treatment composition further comprises a pH modifier.

24. The method of claim 17 , wherein the pH modifier is a carboxylic acid.

25. The method of claim 23 , wherein the pH modifier is lactic acid.

26. The method of claim 23 , wherein the pH modifier is gallic acid.

27. The method of claim 17 , wherein the gelling agent is present in the composition in an amount of from about 0.1 wt/vol % to about 1 wt/vol %.

28. The method of claim 17 , wherein the composition is substantially free of monovalent and divalent salts.

29. The method of claim 17 , wherein the gelling agent includes a low acyl gellan gum.

30. The method of claim 17 , wherein the vaginal treatment composition inhibits the growth of Trichomonas vaginalis .

31. The method of claim 17 , wherein the vaginal treatment composition does not substantially inhibit the growth of Lactobacillus acidophilus .

32. The method of claim 17 , wherein the vaginal treatment composition is substantially free of tonicity agents other than xylitol.

Assignments (1)
NAME CHANGE Recorded Feb 3, 2015
From: KIMBERLY-CLARK WORLDWIDE, INC.
To: KIMBERLY-CLARK WORLDWIDE, INC.
Reel/Frame 034880/0742 →