Methods for Fixing Hair and Skin

• US 20160193129A1
• Filed: 08/05/2015
• Published: 07/07/2016
• Est. Priority Date: 08/01/2013
• Status: Abandoned Application

• Current Assignee: Liqwd, Inc.
• Original Assignee: Liqwd, Inc.
• Inventors: Pressly, Eric D., Hawker, Craig J.
• Application Number:
  US14/819,067
• Publication Number:
  US 20160193129A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: A45D 7/04 chemical
• CPC Class Codes: A61K 2800/884 Sequential application
• CPC Class Codes: A61K 2800/94 Involves covalent bonding to the substrate
• CPC Class Codes: A61K 2800/95 Involves in-situ formation or cross-linking of polymers
• CPC Class Codes: A61K 8/46 containing sulfur A61K8/44 takes precedence
• CPC Class Codes: A61K 8/4913 having five membered rings, e.g. pyrrolidone carboxylic acid
• CPC Class Codes: A61Q 5/002 Preparations for repairing the hair, e.g. hair cure
• CPC Class Codes: A61Q 5/02 Preparations for cleaning the hair
• CPC Class Codes: A61Q 5/04 Preparations for permanent waving or straightening the hair
• CPC Class Codes: A61Q 5/12 Preparations containing hair conditioners

Abstract

Compositions, kits, and methods for repairing bonds, for example, disulfide bonds, in hair or on the skin are disclosed. The compositions provide improved conditioning benefit for dry hair or moisturize the skin. The compositions also provide a long lasting moisturized feel and smooth feel to the skin or hair, without feeling greasy. The compositions contain one or more compounds that covalently crosslink at least two thiol groups in the hair or on the skin. Use of the crosslinking compositions prevents reversion of the repaired bonds to their reduced (thiol) state, for at least one week, one month, six months, or one year, after a single application of the composition. Improved methods of styling hair, for example permanent hair waving, hair curling, and hair straightening are also provided.

Claims

1. A method for treating hair, wherein the hair comprises two or more reduced thiol groups, comprising:

(a) applying to the hair a formulation comprising a crosslinking agent in an effective amount to covalently crosslink the reduced thiol groups,

wherein the crosslinking agent comprises at least two reactive moieties capable of reacting with the reduced thiol groups, and optionally a linker that links the reactive moieties, and the reduced thiol groups are crosslinked via the crosslinking agent at a temperature from about 20°

C. to about 35°

C.

2. The method of claim 1, wherein the crosslinking agent is represented by Formula I:

4. The method of claim 2, wherein each of A, B, C, and D is independently selected from the group consisting of a Michael acceptor, a succinimidyl-containing group, a maleimido-containing group, azlactone, a benzoxazinone derivative, vinyl sulfone, vinyl sulfoximine, benzoxazinone, isocyanate, epoxide, an electrophilic moiety containing a leaving group, an electrophilic thiol acceptor, acrylate group, a methacrylate group, a styrene group, an acryl amide group, a methacryl amide group, a maleate group, a fumarate group, an itaconate group, a vinyl ether group, an allyl ether group, an allyl ester group, and a vinyl ester group.

6. The method of claim 2, wherein A, B, C, and D are the same.

7. The method of claim 2, wherein at least one of A, B, C, and D is different than the other reactive moieties.

8. The method of claim 2, wherein the crosslinking agent has a chemical structure selected from the group consisting of:

9. The method of claim 1, wherein the linker is selected from the group consisting of oxygen, sulfur, carbon, boron, nitrogen, alkoxy, alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, heterocycloalkyl, heteroaryl, ether, amine, and a polymer,

wherein the linker is optionally independently substituted with one or more substituents including hydrogen, halogen, cyano, alkoxy, alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, heterocycloalkyl, heteroaryl, amine, hydroxy, formyl, acyl, carboxylic acid (—

COOH), —

C(O)R¹, —

C(O)OR′

, carboxylate (—

COO⁻

), primary amide (e.g., —

CONH₂), secondary amide (e.g., —

CONHR₁₁), —

C(O)NR¹R², —

NR¹R², —

NR¹S(O)₂R², —

NR¹C(O)R², —

S(O)₂R², —

SR¹, and —

S(O)₂NR¹R², sulfinyl group (e.g., —

SOR₁₁), and sulfonyl group (e.g., —

SOOR₁₁);

wherein R¹ and R² may each independently be hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heterocycloalkyl and heteroaryl;

wherein each of R¹ and R² is optionally independently substituted with one or more substituents selected from the group consisting of halogen, hydroxyl, cyano, nitro, amino, alkylamino, dialkylamino, alkyl optionally substituted with one or more halogen or alkoxy or aryloxy, aryl optionally substituted with one or more halogen or alkoxy or alkyl or trihaloalkyl, heterocycloalkyl optionally substituted with aryl or heteroaryl or ═

O or alkyl optionally substituted with hydroxyl, cycloalkyl optionally substituted with hydroxyl, heteroaryl optionally substituted with one or more halogen or alkoxy or alkyl or trihaloalkyl, haloalkyl, hydroxyalkyl, carboxy, alkoxy, aryloxy, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, and dialkylaminocarbonyl.

10. The method of claim 9, wherein the linker is selected from the group consisting of alkoxy, alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, amine, heterocycloalkyl, and heteroaryl.

11. The method of claim 8, wherein the crosslinking agent is:

12. The method of claim 1, wherein the formulation further comprises one or more pharmaceutically acceptable excipients,

wherein the one or more excipients are selected from the group consisting of water, surfactants, vitamins, natural extracts, preservatives, chelating agents, perfumes, preservatives, antioxidants, chelating agents, hair coloring agents, proteins, amino acids, humectants, fragrances, emollients, penetrants, thickeners, viscosity modifiers, hair fixatives, film formers, emulsifiers, opacifying agents, propellants, liquid vehicles, carriers, salts, pH adjusting agents, neutralizing agents, buffers, hair conditioning agents, anti-static agents, anti-frizz agents, anti-dandruff agents, and combinations thereof.

13. The method of claim 12, wherein the crosslinking agent is present in an amount ranging from about 0.01 wt % to about 50 wt % of the formulation.

17. The method of claim 1, wherein step (a) is repeated one or more times.

19. The method of claim 1, further comprising,

(b) rinsing, shampooing, and/or conditioning the hair, wherein step (b) occurs subsequent to step (a).

20. The method of claim 19, wherein step (b) is performed within about 10 seconds and about 30 minutes after step (a).

21. The method of claim 1, further comprising the step of:

applying a first formulation comprising a reducing agent capable of reducing the disulfide bonds in the hair to produce reduced thiol groups,

wherein the step is performed prior to applying the formulation comprising the crosslinking agent.

22. The method of claim 21, wherein the reducing agent is selected from the group consisting of thioglycolic acid and its derivative salts and esters, thiolactic acid and its derivative salts and esters, cysteine and its derivatives, cysteamine and its derivatives, inorganic sulfites, sodium metabisulfite, other inorganic bisulfites, dithiothreitol, dithioerythritol, organic phosphines, and Japanese relaxers.

27. The method of claim 1, wherein the reactive moieties are not aldehyde, carboxylic acid, or epoxy groups.

3. (canceled)

5. (canceled)

14. (canceled)

15. (canceled)

16. (canceled)

18. (canceled)

23. (canceled)

24. (canceled)

25. (canceled)

26. (canceled)

28. A formulation consisting of a crosslinking agent comprising at least two reactive moieties capable of reacting with reduced thiol groups, an aqueous solvent, and one or more preservatives, stabilizers, or combinations thereof.

29. The formulation of claim 28, wherein the crosslinking agent is represented by Formula I:

30. The formulation of claim 29, wherein the crosslinking agent is: