IP Library Granted Patent US 10,434,073
Granted Patent B2
US 10,434,073 · App. 15/628,449 · Granted Oct 8, 2019

Bakuchiol compositions for treatment of post inflammatory hyperpigmentation

Inventors: Mei Feng Hong (Seattle, WA); Qi Jia (Olympia, WA); Lidia Alfaro Brownell (Tacoma, WA)
Assignee: Unigen, Inc.
A61K31/05A61K8/347A61K31/60A61Q19/02A61K2800/30
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,434,073
App. No.
15/628,449
Granted
Oct 8, 2019
Kind
B2
Abstract

Methods for treating excess pigmentation, including treatment of post inflammatory hyperpigmentation (PIH), are disclosed. The disclosed methods comprise administration of a composition comprising bakuchiol substantially free of furanocoumarins to a mammal. Compositions comprising bakuchiol and methods for their preparation are also disclosed.

Claims (19)

1. A method for alleviating, reducing or treating excess pigmentation in a deep layer of skin resulting from post inflammatory hyperpigmentation derived from acne, the method comprising administering to a mammal an effective amount of a composition comprising bakuchiol, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier and less than 500 ppm total furanocoumarin impurities.

2. The method of claim 1 , wherein the composition comprises less than 100 ppm total furanocoumarin impurities.

3. The method of claim 1 , wherein the composition shows no tyrosinase inhibition activity relative to a kojic acid control.

4. The method of claim 1 , wherein the furanocoumarin impurities comprise psoralen, isopsoralen or combinations thereof.

5. The method of claim 1 , wherein the composition comprises 0.001% to 99.9% by total weight of bakuchiol and a pharmaceutically, dermatologically or cosmetically acceptable carrier.

6. The method of claim 1 , wherein the composition is administered topically, by aerosol, by suppository, intradermically, intramuscularly or intravenously.

7. The method of claim 1 , wherein the composition is formulated for topical administration.

8. The method of claim 1 , wherein the composition comprises from about 0.1% to about 2.0% by total weight of bakuchiol.

9. The method of claim 1 , wherein the composition comprises about 0.5% by total weight of bakuchiol.

10. The method of claim 1 , wherein the method alleviates excess pigmentation.

11. The method of claim 1 , wherein the method reduces excess pigmentation.

12. The method of claim 1 , wherein the method treats excess pigmentation.

13. The method of claim 1 , wherein the excess pigmentation occurs in a papillary dermis layer of skin.

14. The method of claim 1 , further comprising reducing super oxide anion.

15. The method of claim 1 , further comprising reducing melanogenesis.

16. The method of claim 1 , further comprising reducing melanocyte proliferation.

17. The method of claim 1 , further comprising reducing melanocyte apoptosis.

18. The method of claim 1 , wherein the composition further comprises salicylic acid or a pharmaceutically acceptable salt thereof.

19. A method for reducing melanogenesis, reducing melanocyte proliferation or reducing melanocyte apoptosis, wherein the melanogenesis, the melanocyte proliferation, or the melanocyte apoptosis is a result of post inflammatory hyperpigmentation in a deep layer of skin derived from acne, the method comprising administering to a mammal an effective amount of a composition comprising bakuchiol or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier and less than 500 ppm total furanocoumarin impurities.

Continuity (3)
Continuation 13365172
Provisional Application 61438890 · Feb 2, 2011
Related Publication 20170348250A1 · Dec 7, 2017