IP Library Granted Patent US 7,927,614
Granted Patent B2
US 7,927,614 · App. 11/452,642 · Granted Apr 19, 2011

Anti-aging treatment using copper and zinc compositions

Assignee: JR Chem, LLC
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Quick Facts
Patent No.
US 7,927,614
App. No.
11/452,642
Granted
Apr 19, 2011
Kind
B2
Abstract

Composition and methods for alleviating or eliminating age related skin conditions by providing an effective amount of one or more copper, zinc and copper-zinc compositions are disclosed. Treatment is accomplished through the use of topical compositions containing one or more copper or zinc salts and/or copper-zinc compounds or complexes, particularly copper-zinc malonate active ingredient.

Claims (23)

1. A method comprising topically applying to a user's skin a composition comprising a copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule.

2. A method as in claim 1 wherein the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule comprises copper-zinc citrate, copper-zinc oxalate, copper-zinc tartarate, copper-zinc malate, copper-zinc succinate, copper-zinc malonate, copper-zinc maleate, copper-zinc aspartate, copper-zinc glutamate, copper-zinc glutarate, copper-zinc fumarate, copper-zinc glucarate, copper-zinc polyacrylic acid, copper-zinc adipate, copper-zinc pimelate, copper-zinc suberate, copper-zinc azelate, copper-zinc sebacate, copper-zinc dodecanoate, or combinations thereof.

3. A method as in claim 1 wherein the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule is a copper-zinc malonate.

4. A method as in claim 3 wherein the copper-zinc malonate comprises about 16.5% copper and about 12.4% zinc.

5. The method of claim 1 wherein the molar ratio of copper to zinc in the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule is from about 1:1 to about 3:1.

6. The method of claim 1 wherein the molar ratio of copper to zinc in the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule is from about 1:1 to about 2:1.

7. The method of claim 1 wherein the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule is present in an amount from about 0.001 to about 5% by weight of the composition.

8. The method of claim 1 wherein the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule is present in an amount from about 0.05 to about 1% by weight of the composition.

9. The method of claim 1 wherein the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule is present in an amount from about 0.1 to about 0.5% by weight of the composition.

10. A method as in claim 1 wherein the composition is a solution, emulsion, microemulsion, suspension, cream, lotion, gel, powder, solid composition, or combinations thereof.

11. The method according to claim 1 , wherein the composition comprises a dermatologically acceptable carrier or diluent.

12. A method for forming collagen, elastic fibers, elastin, or tropoelastin in the skin of a patient comprising contacting an area of the skin in need thereof with an effective amount of a composition wherein the composition comprises one or more copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule.

13. The method according to claim 12 , wherein the composition comprises a dermatologically acceptable carrier or diluent.

14. The method according to claim 12 , wherein the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule is selected from the group consisting of copper-zinc citrate, copper-zinc oxalate, copper-zinc tartarate, copper-zinc malate, copper-zinc succinate, copper-zinc malonate, copper-zinc maleate, copper-zinc aspartate, copper-zinc glutamate, copper-zinc glutarate, copper-zinc fumarate, copper-zinc glucarate, copper-zinc polyacrylic acid, copper-zinc adipate, copper-zinc pimelate, copper-zinc suberate, copper-zinc azelate, copper-zinc sebacate, copper-zinc dodecanoate, and combinations thereof.

15. The method according to claim 12 , wherein the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule is a copper-zinc malonate.

16. The method according to claim 15 , wherein the copper-zinc malonate comprises about 16.5% copper and about 12.4% zinc.

17. The method according to claim 12 , comprising from about 0.001 to about 5 percent by weight of the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule.

18. The method according to claim 12 , comprising from about 0.05 to about 1 percent by weight of the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule.

19. The method according to claim 12 , comprising from about 0.1 to about 0.5% percent by weight of the copper-zinc carboxylic acid salt having copper and zinc cations in the same molecule.

20. The method of claim 12 wherein the composition further comprises an active drug substance.

21. The method of claim 12 wherein the composition further comprises an active cosmetic substance.

22. The method of claim 12 wherein the composition further comprises humectant, solvent, water, or combinations thereof.

23. The method of claim 12 wherein the composition is in the form of a liquid, cream, oil, gel, fluid cream, lotion, emulsion or microemulsion.

Assignments (17)
RELEASE OF SECURITY INTEREST Recorded Nov 17, 2025
From: TCW ASSET MANAGEMENT COMPANY LLC, AS ADMINISTRATIVE AGENT
To: OBAGI COSMECEUTICALS LLC
Reel/Frame 072928/0385 →
PATENT SECURITY AGREEMENT Recorded Nov 17, 2025
From: OBAGI COSMECEUTICALS LLC
To: LSSF II OFFSHORE INVESTMENTS, LP, AS ADMINISTRATIVE AGENT
Reel/Frame 073625/0459 →
RELEASE OF SECURITY INTEREST Recorded Apr 8, 2025
From: BARCLAYS BANK PLC, AS COLLATERAL AGENT
To: SOLTA MEDICAL, INC.; PRECISION DERMATOLOGY, INC.; BAUSCH HEALTH IRELAND LIMITED (F/K/A/ VALEANT PHARMACEUTICALS IRELAND LIMITED); SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD; SANTARUS, INC.; MEDICIS PHARMACEUTICAL CORPORATION; HUMAX PHARMACEUTICAL S.A.; SOLTA MEDICAL IRELAND LIMITED; BAUSCH & LOMB MEXICO, S.A. DE C.V.; BAUSCH+LOMB OPS B.V.; BAUSCH HEALTH AMERICAS, INC.; BAUSCH HEALTH COMPANIES INC.; BAUSCH HEALTH HOLDCO LIMITED; BAUSCH HEALTH MAGYARORSZAG KFT (A/K/A BAUSCH HEALTH HUNGARY LLC); BAUSCH HEALTH POLAND SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA (F/K/A VALEANT PHARMA POLAND SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA); BAUSCH HEALTH US, LLC; BAUSCH HEALTH, CANADA INC. / SANTE BAUSCH, CANADA INC.; ICN POLFA RZESZOW SPOLKA AKCYJNA (A/K/A ICN POLFA RZESZOW S.A.); ORAPHARMA, INC.; PRZEDSIEBIORSTWO FARMACEUTYCZNE JELFA SPOLKA AKCYJNA (A/K/A PRZEDSIEBIORSTWO FARMACEUTYCZNE JELFA S.A.); SOLTA MEDICAL DUTCH HOLDINGS B.V.; V-BAC HOLDING CORP.; VRX HOLDCO LLC; 1261229 B.C. LTD.; 1530065 B.C. LTD.
Reel/Frame 070778/0199 →
RELEASE OF SECURITY INTEREST Recorded Mar 21, 2025
From: JPMORGAN CHASE BANK, N.A.
To: OBAGI COSMECEUTICALS LLC
Reel/Frame 070592/0979 →
SECURITY INTEREST Recorded Mar 18, 2025
From: OBAGI COSMECEUTICALS LLC
To: TCW ASSET MANAGEMENT COMPANY LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 070546/0595 →
SECURITY INTEREST Recorded Aug 1, 2022
From: OBAGI COSMECEUTICALS LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 060690/0148 →
RELEASE OF SECURITY INTEREST Recorded Jul 29, 2022
From: TCW ASSET MANAGEMENT COMPANY LLC
To: OBAGI COSMECEUTICALS LLC
Reel/Frame 060668/0771 →
RELEASE OF SECURITY INTEREST Recorded Mar 19, 2021
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: OBAGI COSMECEUTICALS LLC
Reel/Frame 055652/0735 →
SECURITY INTEREST Recorded Mar 16, 2021
From: OBAGI COSMECEUTICALS LLC
To: TCW ASSET MANAGEMENT COMPANY LLC, AS COLLATERAL AGENT
Reel/Frame 055613/0083 →
NOTICE OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Dec 13, 2018
From: OBAGI COSMECEUTICALS LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
Reel/Frame 047873/0114 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 11, 2017
From: OBAGI MEDICAL PRODUCTS, INC.
To: OBAGI COSMECEUTICALS LLC
Reel/Frame 044829/0092 →
RELEASE OF SECURITY INTEREST IN SPECIFIED PATENTS Recorded Nov 14, 2017
From: BARCLAYS BANK PLC
To: OBAGI MEDICAL PRODUCTS, INC.
Reel/Frame 044750/0475 →
RELEASE OF SECURITY INTEREST IN SPECIFIED PATENTS Recorded Nov 14, 2017
From: BANK OF NEW YORK MELLON
To: OBAGI MEDICAL PRODUCTS, INC.
Reel/Frame 044750/0506 →
SECURITY INTEREST Recorded Jul 19, 2017
From: OBAGI MEDICAL PRODUCTS, INC.
To: THE BANK OF NEW YORK MELLON
Reel/Frame 043041/0718 →
SECURITY INTEREST Recorded Jul 18, 2016
From: ATON PHARMA, INC.; BAUSCH & LOMB INCORPORATED; BAUSH & LOMB PHARMA HOLDINGS CORP.; DENDREON PHARMACEUTICALS, INC.; DOW PHARMACEUTICAL SCIENCES, INC.; MEDICIS PHARMACEUTICAL CORPORATION; OBAGI MEDICAL PRODUCTS, INC.; OMP, INC.; ORAPHARMA, INC.; PRECISION DERMATOLOGY, INC.; SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD; SANTARUS, INC.; SOLTA MEDICAL, INC.; VALEANT CANADA LP, BY ITS GENERAL PARTNER VALEANT CANADA GP LIMITED; VALEANT PHARMACEUTICALS INTERNATIONAL, INC.; VALEANT HOLDINGS IRELAND (AS SUCCESSOR TO VALEANT INTERNATIONAL BERMUDA); VALEANT PHARMACEUTICALS NORTH AMERICA LLC; VALEANT PHARMACEUTICALS IRELAND
To: BARCLAYS BANK PLC
Reel/Frame 039380/0385 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2014
From: JR CHEM, LLC
To: OBAGI MEDICAL PRODUCTS, INC.
Reel/Frame 032040/0855 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 21, 2006
From: FARYNIARZ, JOSEPH R.; RAMIREZ, JOSE E.
To: JR CHEM, LLC
Reel/Frame 018308/0391 →
Continuity (2)
Provisional Application 60764967 · Feb 3, 2006
Related Publication 20070184017A1 · Aug 9, 2007