IP Library Granted Patent US 7,083,781
Granted Patent B2
US 7,083,781 · App. 10/408,845 · Granted Aug 1, 2006

Film forming polymers, methods of use, and devices and applications thereof

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Quick Facts
Patent No.
US 7,083,781
App. No.
10/408,845
Granted
Aug 1, 2006
Kind
B2
Abstract

Compositions and methods for delivering active agents to the skin of a subject, including a polymer, an active ingredient and a solvent are disclosed, the compositions being capable of delivery by rolling, spreading, aerosol or in droplets and of forming a film in contact with the skin.

Claims (47)

1. A formulation, comprising: an aqueous mixture including a first polyvinyl alcohol having a viscosity in the range of from 38 to 55 cPs, a second polyvinyl alcohol having a viscosity in the range of from 13 to 27 cPs and at least one active agent selected from a pharmaceutical agent, a wound healing agent and a cosmetic agent, but not containing adhesion-promoting polymers other than polyvinyl alcohol, the mixture forming a composition, the composition when dried forming an agent releasing, water removable, peelable film when applied to a skin surface.

2. A formulation according to claim 1 , wherein the pharmaceutical agent is an agent selected from the group consisting of: an anti-inflammatory, a local anesthetic, a xanthine derivative, an antihistaminic, an antifungal, an antimicrobial, an antibiotic, a cardiovascular, a hormone, an erectile dysfunction treatment, a vasodilator, an antirheumatoid, a chemotherapy, an adrenergic agonist or an adrenergic antagonist.

3. A formulation according to claim 1 , wherein one or more cosmetic agents are selected from the group consisting of: anti-irritant, anti-oxidant, skin conditioning, anti-blotching, anti-aging, anti-cellulite, skin firming, eye contour, slimming, sooth, sunburn, skin lifting, anti-elastase, anti-collagenase, free radical scavenger, seboregulator, hydrative, vitamin, mineral, a-hydroxy acid, and anti-hyperpigmentation agents.

4. A formulation according to claim 1 , wherein the composition is in the form of a gel.

5. A formulation according to claim 1 , wherein the first polyvinyl alcohol and second polyvinyl alcohol are present at about 6 to 8% and 4 to 5%, respectively, on a wet weight basis with respect to the total composition.

6. A formulation according to claim 1 , wherein the ratio of first polyvinyl alcohol to second polyvinyl alcohol is about 3:2.

7. A formulation according to claim 1 wherein the film is at least translucent.

8. A formulation according to claim 7 wherein the film is transparent.

9. A formulation according to claim 1 wherein the film is between 0.01 and 0.25mm thick.

10. A formulation according to claim 1 wherein the film is 0.03 to 0.1mm thick.

11. A method for administering a dosage of at least one active agent to a site on a subject, comprising:

(i) providing a formulation, the formulation including a first polyvinyl alcohol having a viscosity in the range of from 38 to 55 cPs, a second polyvinyl alcohol having a viscosity in the range of from 13 to 27 cPs, water and at least one active agent selected from one or more of a pharmaceutical agent, a wound healing agent and a cosmetic agent;

(ii) releasing from a container, a quantity of the formulation onto skin of the subject so as to form a quick-drying, agent releasing, water removable, peelable film capable of overnight adhesion and containing the active agent, wherein polymers contributing to said overnight adhesion consist of the first and second polyvinyl alcohols; and

(iii) a administering the agent to the subject from the film.

12. A method according to claim 11 , wherein the first polyvinyl alcohol and the second polyvinyl alcohol, each present at about 1 to 10%, on a wet weight basis with respect to the total composition.

13. A method according to claim 11 , wherein the first polyvinyl alcohol and the second polyvinyl alcohol are present at about 6 to 8% and 4 to 5%, respectively, on a wet weight basis with respect to the total composition.

14. A method according to claim 11 , wherein at least one agent is selected from the group consisting of: an anti-inflammatory, a local anesthetic, a xanthine derivative, an antihistaminic, an antifungal, an antimicrobial, an antibiotic, a cardiovascular, a hormone, an erectile dysfunction treatment, a vasodilator, an antirheumatoid, a chemotherapy, an adrenergic agonist, an adrenergic antagonist, an anti-irritant, an anti-oxidant, a skin conditioning, an anti-blotching, an anti-aging, an anti-cellulite, a skin firming, a eye contour, a slimming, a sunburn soothing, a skin lifting, an anti-elastase, an anti-collagenase, a free radical scavenger, a seboregulator, a hydrative, a vitamin, a mineral, an a-hydroxy acid, and an anti-hyperpigmentation agents.

15. A method according to claim 11 wherein the film is at least translucent.

16. A method according to claim 15 wherein the film is transparent.

17. A method according to claim 11 wherein the film is between 0.01 and 0.25 mm thick.

18. A method according to claim 11 wherein the film is between 0.03 and 0.1 mm thick.

19. A method according to claim 11 wherein administering includes percutaneous absorption of the agent.

20. A method for administering a dosage of at least one active agent to a subject, comprising:

(i) applying to a skin surface of the subject, an amount of a formulation containing water, a first polyvinyl alcohol having a viscosity in the range of from 38 to 55 cPs, a second polyvinyl alcohol having a viscosity in the range of from 13 to 27 cPs and the active agent selected from one or more of a pharmaceutical agent, a wound healing agent and a cosmetic agent but not containing adhesion-promoting polymers other than to polyvinyl alcohol;

(ii) allowing the formulation to dry on the skin to form a peelable, water-removable agent-releasing film containing the active agent; and

(iii) administering the dosage of the active agent to the subject from the wet formulation and then from the film.

21. A method according to claim 20 , wherein the formulation is administered from a container selected from the group consisting of: an aerosol can, an atomizer, a jar having an apical manual pump, a rollette and a tube container.

22. A method according to claim 21 , wherein the formulation is administered in a controlled dosage.

23. A method according to claim 20 wherein the film is at least translucent.

24. A method according to claim 23 wherein the film is transparent.

25. A method according to claim 20 wherein the film is between 0.01 and 0.25 mm thick.

26. A method according to claim 20 wherein the film is between 0.03 and 0.1 mm thick.

27. A method according to claim 20 wherein administering is performed by percutaneous absorption of the active agent.

28. An active agent delivery system comprising:

a peelable agent-releasing film dried on the skin of a subject so as to be at least translucent, the film administering a dosage of active agent contained in the film into the subject through percutaneous absorption, wherein the film was made from a first polyvinyl alcohol having a viscosity in the range of from 38 to 55 cPs and a second polyvinyl alcohol having a viscosity in the range of from 13 to 27 cPs but not from adhesion-promoting polymers besides polyvinyl alcohol.

29. The active agent delivery system of claim 28 wherein the film has a thickness between 0.01 to 0.25 mm.

30. The active agent delivery system of claim 28 wherein the film has a thickness between 0.03 and 0.1 mm.

31. The active agent delivery system of claim 28 wherein the active agent is a pharmaceutical agent.

32. The active agent delivery system of claim 28 wherein the active agent is a wound healing agent.

33. The active agent delivery system of claim 28 wherein the film is transparent.

34. A method for administering a dosage of at least one active agent to a subject, comprising:

(i) applying to a skin surface of the subject, an amount of a gel formulation containing water, a first polyvinyl alcohol having a viscosity in the range of from 38 to 55 cPs, a second polyvinyl alcohol having a viscosity in the range of from 13 to 27 cPs and the active agent selected from one or more of a pharmaceutical agent, a wound healing agent and a cosmetic agent;

(ii) allowing the gel formulation to dry on the skin to form a peelable, water-removable, agent-releasing film capable of overnight adhesion and containing the active agent wherein polymers contributing to said overnight adhesion consist of the first and second polyvinyl alcohols; and

(iii) administering by percutaneous absorption, the dosage of the active agent to the subject from the gel and then from the film.

35. A formulation, comprising: an aqueous mixture including a first polyvinyl alcohol having a viscosity in the range of from 38 to 55 cPs, a second polyvinyl alcohol having a viscosity in the range of from 13 to 27 cPs and at least one active agent selected from a pharmaceutical agent, a wound healing agent and a cosmetic agent, the mixture forming a composition, the composition when dried forming an agent releasing, water removable, peelable film capable of overnight adhesion when applied to a skin surface wherein polymers contributing to said overnight adhesion consist of said first and second polyvinyl alcohols.

36. An active agent delivery system comprising:

a peelable agent-releasing film dried on the skin of a subject so as to be capable of overnight adhesion and at least translucent, the film administering a dosage of active agent contained in the film into the subject, wherein the film was made from a first polyvinyl alcohol having a viscosity in the range of from 38 to 55 cPs and a second polyvinyl alcohol having a viscosity in the range of from 13 to 27 cPs wherein polymers contributing to said overnight adhesion consist of said first and second polyvinyl alcohols.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 28, 2016
From: LAVIPHARM LABORATORIES, INC.
To: THALLIUM HOLDING COMPANY, LLC
Reel/Frame 037610/0699 →
ASSIGNMENT OF SECURITY INTEREST Recorded Jan 28, 2016
From: MEDICAL PROVIDER FINANCIAL CORPORATION, III
To: THALLIUM HOLDING COMPANY, LLC
Reel/Frame 037627/0778 →
SECURITY AGREEMENT Recorded Jan 23, 2006
From: LAVIPHARM LABORATORIES, INC.
To: MEDICAL PROVIDER FINANCIAL CORPORATION, III
Reel/Frame 017050/0835 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 15, 2003
From: FOTINOS, SPIROS; TSARDAKA, EKATERINI; KOBOROZOS, GEORGE
To: LAVIPHARM S.A.
Reel/Frame 014395/0232 →