IP Library Granted Patent US 10,597,402
Granted Patent B2
US 10,597,402 · App. 15/277,990 · Granted Mar 24, 2020

Compositions and methods for restoring epidermal integrity and function and treating dermatological diseases

Inventor: Ratan K Chaudhuri (Lincoln Park, NJ)
Assignee: Sytheon Limited
C07D493/04A61K8/4973A61K9/0014A61K9/0053A61K31/34A61K45/06A61Q17/04A61Q19/007A61Q19/08A61K2800/74
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 10,597,402
App. No.
15/277,990
Granted
Mar 24, 2020
Kind
B2
Abstract

Novel isohexide esters and isohexide compositions are prepared and used in improving skin health and condition.

Claims (32)

1. A topical composition comprising

a) an isohexide according to Structure 1

wherein R 1 and R 2 , which are the same or different, are independently selected from H and a C 15 to C 19 saturated or unsaturated n-alkyl carboxylate group, provided that both R 1 and R 2 are not hydrogen, in combination with

b) one or more additional isohexides according to Structure 1 wherein the isohexide is a different isomer from that of isohexide (a) or at least one of R 1 and R 2 , is different from the R 1 and R 2 of isohexide (a), or both, provided that the limitations of (a) with respect to R 1 and R 2 are still met, or

c) one or more isohexides corresponding to Structure 5

wherein R 4 and R 5 are the same or different and are independently selected from H and saturated or unsaturated n-alkyl carboxylate groups provided that the n-alkyl carboxylate groups are other than n-alkyl carboxylate groups of 15 to 19 carbon atoms and provided that both R 4 and R 5 are not H, or

d) both (b) and (c),

in a dermatologically acceptable carrier, said isohexides comprising 0.5 to 30 weight percent of the topical composition and the carbon number for the n-alkyl carboxylate groups referring the number of carbon atoms of the group excluding the carboxylate carbon.

2. The composition of claim 1 wherein one of R 1 and R 2 of isohexide (a) is H.

3. The composition of claim 1 wherein R 1 and R 2 of isohexide (a) are the same and are selected from n-alkyl carboxylate groups having from 16 to 19 carbon atoms.

4. The composition of claim 1 wherein at least one of R 1 and R 2 of isohexide (a) has 17 carbon atoms.

5. The composition of claim 1 wherein both R 1 and R 2 of isohexide (a) have 17 carbon atoms.

6. The composition of claim 1 wherein at least one of R 1 and R 2 of isohexide (a) is a mono- or poly-unsaturated n-alkyl carboxylate group.

7. The composition of claim 1 wherein at least one of R 1 and R 2 of isohexide (a) is a poly-unsaturated n-alkyl carboxylate group.

8. The composition of claim 1 wherein the isohexides are isosorbides, isomannides or isoiodides or a combination of any two or all three.

9. The composition of claim 1 wherein isohexide (a) is an isosorbide.

10. The composition of claim 1 wherein a mixture of isohexides according to Structure 1 are present, and at least 50 mole % of those isohexides are isosorbides.

11. The composition of claim 1 wherein a mixture of isohexides according to Structure 1 are present, and at least 40 mole % of the n-alky carboxylate groups of those isohexides are the same.

12. The composition of claim 1 wherein a mixture of isohexides according to Structure 1 are present, and at least 70 mole % of the n-alky carboxylate groups of those isohexides are the same.

13. The composition of claim 1 wherein a mixture of isohexides according to Structure 1 are present and both R 1 and R 2 of isohexide (b) are different from the R 1 and R 2 of the isohexide (a).

14. The composition of claim 1 wherein at least one isohexide according to Structure 5, isohexide (c), is present.

15. The composition of claim 14 wherein the n-alkyl group(s) R 4 and R 5 of Structure 5 have from 1 to 10 carbon atoms.

16. The composition of claim 14 wherein the n-alkyl group(s) R 4 and R 5 of Structure 5 have from 1 to 9 carbon atoms.

17. The composition of claim 14 wherein at least 50% by weight of the isohexides comprise one or more isohexides according to Structure 1.

18. The composition of claim 14 wherein at least 70% by weight of the isohexides comprise one or more isohexides according to Structure 1.

19. The isohexide composition of claim 1 which is the reaction product of a dianhydrohexitol material and a natural oil containing a plurality of fatty acids having from 16 to 20 carbon atoms and/or the triglyceride precursor of said fatty acids.

20. The isohexide composition of claim 19 wherein the natural oil contains a combination saturated and/or unsaturated fatty acids of from 16 to 20 carbon atoms.

21. The isohexide composition of claim 19 wherein the natural oil contains a combination of mono- and/or poly-unsaturated fatty acids of 16 to 20 carbon atoms.

22. The isohexide composition of claim 19 wherein the natural oil is selected from the group consisting of oils isolated from safflower, grape seed, silybum marianum , hemp, sunflower, wheat germ, pumpkin seed, sesame, rice bran, almond, rapeseed, peanut, olive, and coconut.

23. The composition of claim 1 further comprising one or more skin care actives or therapeutic agents.

24. The isohexide composition of claim 19 wherein the dianhydrohexitol is isosorbide, isomannide or isoiodide or a combination of any two or all three.

25. The isohexide composition of claim 19 wherein the natural oil is sunflower oil.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 12, 2016
From: CHAUDHURI, RATAN K
To: SYTHEON LTD
Reel/Frame 040708/0616 →
Continuity (4)
Continuation In Part 15081898 · Mar 27, 2016
Provisional Application 62378217 · Aug 23, 2016
Provisional Application 62139619 · Mar 27, 2015
Related Publication 20170081339A1 · Mar 23, 2017