IP Library › Granted Patent US 10,543,167
Granted Patent B2
US 10,543,167 · App. 14/711,383 · Granted Jan 28, 2020

Topical composition containing antioxidants

Inventors: Aldo Laghi (St. Petersburg, FL); Nathaniel Vint (St. Petersburg, FL)
Assignee: ALPS SOUTH EUROPE S.R.O.
A61K9/0014A61K9/107A61K31/216A61K47/06A61K47/44
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Quick Facts
Patent No.
US 10,543,167
App. No.
14/711,383
Granted
Jan 28, 2020
Kind
B2
Abstract

Disclosed herein are compositions for topical application that effectively deliver antioxidants across the epidermis, dermis, or a combination thereof into cells and/or the bloodstream while concurrently maintaining chemical activity of the antioxidants. In certain aspects, these formulations include emulsions and balms each having a lipophilic carrier and a lipophilic antioxidant solubilized by the lipophilic carrier. Also disclosed herein are methods for making these compositions for topical application.

Claims (77)

1. An emulsion for topical application comprising:

a water phase ranging 60-90% of the overall emulsion, and

an oil phase, wherein:

the oil phase comprises a lipophilic carrier, a skin penetration enhancer, an additive selected from the group consisting of aloe vera extract, D-Ascorbic Acid, L-Ascorbic Acid, D and L-Ascorbic Acid solution, glycerin, lilac, and silicone, the additive ranging from more than 18% to 40% of the overall emulsion, and a lipophilic antioxidant solubilized by the lipophilic carrier and forming a suspension,

the lipophilic carrier and the lipophilic antioxidant being present from 1:1 to 20:1 of lipophilic carrier to lipophilic antioxidant in the emulsion, the lipophilic antioxidant having been powderized to a particle diameter size selected from the group consisting of 40 nm to 5 μm, 40 nm to 1 μm, 40 nm to 900 nm, 40 nm to 750 nm, 40 nm to 500 nm, 50 nm to 400 nm, 40 nm to 300 nm, 50 nm to 250 nm, 40 nm to 100 nm, and 40 nm to 70 nm prior to being solubilized by the lipophilic carrier, and

the lipophilic antioxidant having one of the following formulas (I) to (III):

wherein:

R 1 represents a C 1 to C 9 linear or branched alkyl group or styrene;

R 2 is optional and represents a C 1 to C 6 linear or branched alkyl group or styrene;

Y 1 represents a C 1 to C 6 linear or branched alkyl group, styrene, —SR 5 , or —(CH 2 ) n COOR 6 ;

R 3 and R 4 independently represent a C 1 to C 6 branched alkyl;

Y 2 represents a C 1 to C 6 linear or branched alkyl group, —SR 5 , or —(CH 2 ) n COOR 6 ;

Y 3 represents a linear or branched alkyl group;

n is from 1 to 10;

R 5 represents isoprene, a methyl group, an ethyl group, a propyl, a butyl, a pentyl group, a hexyl group, an isopropyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a tert-pentyl group, a neo-pentyl group, an isopentyl group, an isohexyl group, a neohexyl group, styrene, or

wherein R 11 , R 12 , and R 13 independently represent OH, a methyl group, ethyl group, a propyl group, a butyl group, an isopropyl group, a tert-butyl group, an isoprene, or a tert-pentyl group, and

R 6 represents an alkyl group having C 10 to C 30 ; and

wherein formulas (I) to (III) include pharmaceutically acceptable salts thereof.

2. The emulsion of claim 1 , wherein the C 1 to C 6 linear or branched alkyl groups of Y 1 and Y 2 are substituted with

wherein:

R 7 represents

wherein:

R 8 , R 9 , and R 10 independently represent OH, a methyl group, ethyl group, a propyl group, a butyl group, an isopropyl group, a tert-butyl group, an isoprene, or a tert-pentyl group;

at least one of R 8 , R 9 , and R 10 is OH; and

R 8 , R 9 , and R 10 can be in any of the ortho, meta, and para positions relative to each other.

3. The emulsion of claim 1 , wherein the emulsion includes at least two lipophilic antioxidants from formulas (I) to (III).

4. The emulsion of claim 1 , wherein the emulsion includes at least three lipophilic antioxidants from formulas (I) to (III).

5. The emulsion of claim 1 , wherein the lipophilic carrier and the lipophilic antioxidant are present from 1:1 to 10:1 of lipophilic carrier to lipophilic antioxidant in the emulsion.

6. The emulsion of claim 1 , wherein the lipophilic carrier and the lipophilic antioxidant are present from 1:1 to 1:5 of lipophilic carrier to lipophilic antioxidant in the emulsion.

7. The emulsion of claim 1 , wherein the oil phase ranges from 10 wt % to 40 wt % of the overall emulsion.

8. The emulsion of claim 5 , wherein the oil phase ranges from 10 wt % to 40 wt % of the overall emulsion.

9. The emulsion of claim 1 , wherein the lipophilic carrier comprises at least one of a mineral oil, vegetable oil, or combinations thereof.

10. The emulsion of claim 9 , wherein the mineral oil is a paraffinic oil.

11. The emulsion of claim 9 , wherein the mineral oil is a naphthenic oil.

12. The emulsion of claim 1 , wherein the lipophilic carrier includes at least one selected from the group consisting of argan oil, avocado oil, babassu oil, canola oil, coconut oil, hemp seed oil, jojoba oil, olive oil, and rosehip oil.

13. The emulsion of claim 1 , wherein the lipophilic carrier is avocado butter, mango butter, shea butter, cocoa butter, or any combination thereof.

14. A method for making an emulsion for topical application comprising:

providing water and a vegetable or mineral oil,

providing a powdered lipophilic antioxidant having a particle diameter size selected from the group consisting of 40 nm to 5 μm, 40 nm to 1 μm, 40 nm to 900 nm, 40 nm to 750 nm, 40 nm to 500 nm, 50 nm to 400 nm, 40 nm to 300 nm, 50 nm to 250 nm, 40 nm to 100 nm, and 40 nm to 70 nm, and

mixing the water and the vegetable or mineral oil with a surfactant to form the emulsion, wherein the emulsion includes:

a water phase ranging 60-90% of the overall emulsion, and

an oil phase, wherein:

the oil phase comprises a lipophilic carrier, a skin penetration enhancer, an additive selected from the group consisting of aloe vera extract, D-Ascorbic Acid, L-Ascorbic Acid, D and L-Ascorbic Acid solution, glycerin, lilac, and silicone, the additive ranging from more than 18% to 40% of the overall emulsion, and a lipophilic antioxidant solubilized by the lipophilic carrier forming a suspension,

the lipophilic carrier and the lipophilic antioxidant being present from 1:1 to 1:20 of lipophilic carrier to lipophilic antioxidant in the emulsion, and

the lipophilic antioxidant having one of the following formulas (I) to (III):

wherein,

R 1 represents a C 1 to C 9 linear or branched alkyl group or styrene;

R 2 is optional and represents a C 1 to C 6 linear or branched alkyl group or styrene;

Y 1 represents a C 1 to C 6 linear or branched alkyl group, styrene, —SR 5 , or —(CH 2 ) n COOR 6 ;

R 3 and R 4 independently represent a C 1 to C 6 branched alkyl;

Y 2 represents a C1 to C 6 linear or branched alkyl group, —SR 5 , or —(CH 2 ) n COOR 6 ;

Y 3 represents a linear or branched alkyl group;

n is from 1 to 10;

R 5 represents isoprene, a methyl group, an ethyl group, a propyl, a butyl, a pentyl group, a hexyl group, an isopropyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a tert-pentyl group, a neo-pentyl group, an isopentyl group, an isohexyl group, a neohexyl group, styrene, or

wherein R 11 , R 12 , and R 13 independently represent OH, a methyl group, ethyl group, a propyl group, a butyl group, an isopropyl group, a tert-butyl group, an isoprene, or a tert-pentyl group,

R 6 represents an alkyl group having C 10 to C 30 ; and

wherein formulas (I) to (III) included pharmaceutically acceptable salts thereof.

15. The method of claim 14 , wherein the water and the vegetable or mineral oil with the surfactant are mixed at a temperature ranging from 100° F. to 150° F. for 5 to 60 minutes to form the emulsion.

16. A balm for topical application comprising:

a lipophilic carrier, a skin penetration enhancer, an additive selected from the group consisting of aloe vera extract, D-Ascorbic Acid, L-Ascorbic Acid, D and L-Ascorbic Acid solution, glycerin, lilac, and silicone, the additive ranging from more than 18% to 40% of the overall emulsion, and a lipophilic antioxidant solubilized by the lipophilic carrier forming a suspension,

the lipophilic carrier and the lipophilic antioxidant being present from 1:1 to 1:20 of lipophilic carrier to lipophilic antioxidant in the emulsion, the lipophilic antioxidant having been powderized to a particle diameter size selected from the group consisting of 40 nm to 5 μm, 40 nm to 1 μm, 40 nm to 900 nm, 40 nm to 750 nm, 40 nm to 500 nm, 50 nm to 400 nm, 40 nm to 300 nm, 50 nm to 250 nm, 40 nm to 100 nm, and 40 nm to 70 nm prior to being solubilized by the lipophilic carrier, and

The lipophilic antioxidant having one of the following formulas (I) to (III):

wherein,

R 1 represents a C 1 to C 9 linear or branched alkyl group or styrene;

R 2 is optional and represents a C 1 to C 6 linear or branched alkyl group or styrene;

Y 1 represents a C 1 to C 6 linear or branched alkyl group, styrene, —SR 5 , or —(CH 2 ) n COOR 6 ;

R 3 and R 4 independently represent a C1 to C6 branched alkyl;

Y 2 represents a C 1 to C 6 linear or branched alkyl group, —SR 5 , or —(CH 2 ) n COOR 6 ;

Y 3 represents a linear or branched alkyl group;

n is from 1 to 10;

R 5 represents isoprene, a methyl group, an ethyl group, a propyl, a butyl, a pentyl group, a hexyl group, an isopropyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a tert-pentyl group, a neo-pentyl group, an isopentyl group, an isohexyl group, a neohexyl group, styrene, or

wherein R 11 , R 12 , and R 13 independently represent OH, a methyl group, ethyl group, a propyl group, a butyl group, an isopropyl group, a tert-butyl group, an isoprene, or a tert-pentyl group,

R 6 represents an alkyl group having C 10 to C 30 ; and

wherein formulas (I) to (III) include pharmaceutically acceptable salts thereof.

17. The emulsion of claim 1 , wherein the skin penetration enhancer is an organic solvent.

18. The method of claim 14 , wherein the skin penetration enhancer is an organic solvent.

19. The balm of claim 16 , wherein the skin penetration enhancer is an organic solvent.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2015
From: LAGHI, ALDO; VINT, NATHANIEL
To: ALPS SOUTH EUROPE S.R.O.
Reel/Frame 035631/0952 →
Continuity (2)
Provisional Application 62051534 · Sep 17, 2014
Related Publication 20160074319A1 · Mar 17, 2016