Compositions and methods for the treatment of bacterial vaginosis
Described herein are methods and formulations for treating, inhibiting, or ameliorating vaginitis, including bacterial vaginosis. Aspects described herein relate to formulations including a reactive oxygen species, a rheology agent, and a silicone polymer and methods of using these formulations for treating, ameliorating, or inhibiting a vaginitis, including bacterial vaginosis.
1. A method of promoting vaginal health in a subject, comprising:
topically administering to a vaginal region of a subject a composition comprising:
a reactive oxygen species;
a rheology agent;
a silicone polymer; and
hydrochloric acid,
wherein the composition has a pH ranging from about 6.0 to about 7.5,
whereby, topically administering the composition promotes a healthy vaginal microenvironment by maintaining healthy vaginal microbiota.
2. The method of claim 1 , wherein topically administering the composition prevents or treats bacterial vaginosis.
3. The method of claim 1 , wherein the reactive oxygen species is hypochlorite.
4. The method of claim 1 , wherein the reactive oxygen species is present in an amount of about 50 to about 100 ppm.
5. The method of claim 1 , wherein the reactive oxygen species is present in an amount of about 60 ppm.
6. The method of claim 1 , wherein the rheology agent is sodium magnesium silicate.
7. The method of claim 1 , wherein the rheology agent is present in an amount of about 0.1%, 0.25%, 0.5%, 0.75%, 1%, 1.5%, 2%, 2.5%, 3%, 3.5%, 4%, 4.5%, 5%, 6%, 7%, 10%, or 15% w/v.
8. The method of claim 1 , wherein the rheology agent is present in an amount of about 3% w/v.
9. The method of claim 1 , wherein the silicone polymer is dimethicone.
10. The method of claim 1 , wherein the silicone polymer is present in an amount of about 0.5%, 1%, 5%, 10%, 15%, 20%, 30%, 40%, or 50% w/v.
11. The method of claim 1 , wherein the silicone polymer is present in an amount of about 10% w/v.
12. The method of claim 1 , wherein the pH adjuster is present in an amount of about 0.01%, 0.02%, 0.03%, 0.04%, 0.05%, 0.06%, 0.07%, 0.08%, 0.09%, 0.1%, 0.2%, 0.3%, 0.4%, 0.5%, 0.6%, 0.7%, 0.8%, 0.9%, or 1% w/v.
13. The method of claim 1 , wherein the pH adjuster is present in an amount of about 0.08% w/v.
14. The method of claim 1 , wherein the composition further comprises water.
15. The method of claim 1 , wherein the composition comprises hypochlorite in an amount of about 60 ppm, sodium magnesium silicate in an amount of about 3% w/v, dimethicone in an amount of about 10% w/v, hydrochloric acid in an amount of about 0.08% w/v, and water in an amount of about 90% w/v.
16. The method of claim 1 , wherein the healthy vaginal microbiota comprises bacteria of the genus Lactobacillus.
17. The method of claim 1 , wherein topically administering the composition reduces secretion of pro-inflammatory cytokines from vaginal epithelial.
18. The method of claim 17 , wherein the pro-inflammatory cytokines is IL-8.
19. The method of claim 1 , wherein topically administering the composition prevents an inflammatory response in a vaginal microenvironment.
20. The method of claim 1 , wherein topically administering the composition activates a nuclear factor-like 2 (Nrf2) related pathway.
21. The method of claim 20 , wherein the activation of Nrf2 related pathway prevents oxidative damage.
22. The method of claim 1 , wherein the administration of the composition increases glutathione secretion in the vaginal microenvironment.
23. The method of claim 1 , wherein topically administering the composition reduces abnormal vaginal microflora comprising Gardnerella vaginalis, Atopobium vaginae, Megasphaera , or BVAB2.