METHOD FOR PERMANENTLY RESHAPING KERATIN FIBERS WITH AN ACID PRE-TREATING COMPOSITION

• US 20090252697A1
• Filed: 04/08/2009
• Published: 10/08/2009
• Est. Priority Date: 04/08/2008
• Status: Abandoned Application

• Current Assignee: L'Oreal SA
• Original Assignee: L'Oreal SA
• Inventors: NUZZO, Stefania, BARBARAT, Philippe
• Application Number:
  US12/420,423
• Publication Number:
  US 20090252697A1
• Time in Patent Office: Days
• US Class Current: 424/70.500
• CPC Class Codes: A61K 2800/884 Sequential application
• CPC Class Codes: A61K 8/19 containing inorganic ingredients
• CPC Class Codes: A61K 8/20 Halogens; Compounds thereof
• CPC Class Codes: A61K 8/365 Hydroxycarboxylic acids; Ketocarboxylic acids
• CPC Class Codes: A61K 8/43 Guanidines
• CPC Class Codes: A61Q 5/04 Preparations for permanent waving or straightening the hair

Abstract

A method for permanently reshaping keratin fibers, such as hair, comprising applying onto the keratin fibers a pre-treating composition comprising, in a cosmetically acceptable medium, at least one entity chosen from non reducing inorganic acids, non reducing organic acids, and salts thereof, wherein the pH value of said pre-treating composition ranges from 2 to 5; rinsing the keratin fibers; applying onto the keratin fibers a treating composition comprising, in a cosmetically acceptable medium, at least one hydroxide compound; and reshaping the keratin fibers, wherein the reshaping occurs after applying the pre-treating composition and at any time before, during, or after applying the treating composition.

Claims

1. A method for permanently reshaping keratin fibers, comprising:

applying onto the keratin fibers a pre-treating composition comprising, in a cosmetically acceptable medium, at least one entity chosen from non reducing inorganic acids, non reducing organic acids, and salts thereof, wherein the pH value of said pre-treating composition ranges from 2 to 5,

rinsing the keratin fibers,

applying onto the keratin fibers a treating composition comprising, in a cosmetically acceptable medium, at least one hydroxide compound, and

reshaping the keratin fibers, wherein the reshaping occurs after applying the pre-treating composition and at any time before, during, or after applying the treating composition.

2. A method according to claim 1, wherein the at least one non reducing inorganic acid is selected from mono- and polyacids.

3. A method according to claim 2, wherein the at least one non reducing inorganic acid is selected from hydrochloric acid, phosphoric acid, sulfuric acid, and boric acid.

4. A method according to claim 1, wherein the at least one non reducing organic acid comprises at least one functional group chosen from carboxylic, sulfonic, phosphonic, and phosphoric acid functional groups.

5. A method according to claim 4, wherein the at least one non reducing organic acid is a monocarboxylic acid selected from hydroxylated, non-hydroxylated, aliphatic, and aromatic acids.

6. A method according to claim 5, wherein the at least one non reducing monocarboxylic, organic acid is selected from acetic acid, trichloroacetic acid, propanoic acid, butanoic acid, phenyl acetic acid, salicylic acid, benzylic acid, glycolic acid, lactic acid, ascorbic acid, salicylic acid derivatives, jasmonic acid derivative, 3-hydroxy-2-pentyl-cyclopentyl acetic acid, pyruvic acid, and mandelic acid.

7. A method according to claim 4, wherein the at least one non reducing organic acid is a polycarboxylic acid selected from aspartic acid, glutamic acid, oxalic acid, succinic acid, tartaric acid, mucic acid, citric acid, malic acid, maleic acid, phthalic acid, poly(ethylene glycol) bis(carboxymethyl)ethers, acrylic polyacid, copolymer of acrylic acid and maleic acid, polyaspartic acid, and carboxylic polydimethylsiloxanes.

8. A method according to claim 4, wherein the at least one non reducing organic acid is a sulfonic acid selected from benzene sulfonic acid, sulfonic acid HSO₂OH, taurine, 2-[4-(2-hydroxy-ethyl)-piperazin-1-yl]ethane sulfonic acid (or HEPES), and (3E)-3-(4-{(E)-[7,7-dimethyl-3-oxo-4-(sulfomethyl)bicyclo[2.2.1]hept-2-ylidene]methyl}benzylidene)-7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl]methane sulfonic acid.

9. A method according to claim 1, wherein the at least one non reducing organic acid is selected from trichloroacetic acid, L-glutamic acid, lactic acid, succinic acid, DL tartaric acid, poly(ethylene glycol) bis(carboxymethyl)ether having a molecular weight of 250 g/mol, salicylic acid derivatives, jasmonic acid derivative, 3-hydroxy-2-pentyl-cyclopentyl acetic acid, 2-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-ethanesulfonic acid, malic acid, pyruvic acid, and mandelic acid.

10. A method according to claim 1, wherein the at least one non reducing organic acid is selected from citric acid, acetic acid, salicylic acid, and glycolic acid.

11. A method according to claim 1, wherein the pre-treating composition is at a temperature ranging from 25 to 60°

C.

12. A method according to claim 1, wherein the pre-treating composition is allowed to stand for a period of exposure time ranging from 10 to 60 minutes.

13. A method according to claim 1, further comprising wringing the keratin fibers, wherein the wringing occurs after the fibers are rinsed and before the treating composition is applied.

14. A method according to claim 1, wherein the at least one hydroxide compound is selected from alkaline metal hydroxides, alkaline earth metal hydroxides, transition metal hydroxides, lanthanide metal hydroxides, actinide metal hydroxides, Group III hydroxides, Group IV hydroxides, Group V hydroxides, Group VI hydroxides, organic hydroxides, and compounds comprising at least one partially hydrolyzable, hydroxide substituent.

15. A method according to claim 14, wherein the at least one hydroxide compound is selected from sodium hydroxide, guanidinium hydroxide, lithium hydroxide, calcium hydroxide, barium hydroxide, potassium hydroxide, magnesium hydroxide, aluminium hydroxide, copper hydroxide, and zinc hydroxide.

16. A method according to claim 15, wherein the at least one hydroxide compound is selected from sodium hydroxide and guanidinium hydroxide.

17. A method according to claim 1, wherein the treating composition is in the form of an emulsion.

18. A method according to claim 1, wherein the at least one hydroxide compound is present in the treating composition in an amount ranging from 0.2 to 1M.

19. A method according to claim 1, wherein the treating composition is at a temperature ranging from 20 to 40°

C.

20. A method according to claim 1, wherein the treating composition is allowed to react for a period of exposure time ranging from 5 to 60 minutes.

21. A method according to claim 1, wherein the keratin fibers are rinsed off after the treating composition is applied.

22. A method according to claim 1, further comprising applying onto the keratin fibers a post-treating composition comprising, in a cosmetically acceptable medium, at least one entity selected from inorganic acids, organic acids, and salts thereof.

23. A method according to claim 22, wherein the at least one organic acid present in the post-treating composition is selected from saturated and unsaturated acids comprising at least one functional group selected from carboxylic, sulfonic, phosphonic, and phosphoric acid functional groups.

24. A method according to claim 23, wherein the at least one organic acid present in the post-treating composition is selected from acetic acid, lactic acid, glycolic acid, ascorbic acid, malic acid, benzylic acid, succinic acid, taurine, tartaric acid, and citric acid.

25. A method according to claim 22, wherein the at least one inorganic acid is selected from mono- and polyacids.

26. A method according to claim 25, wherein the at least one inorganic acid is selected from hydrochloric acid, phosphoric acid, sulfuric acid, and boric acid.

27. A cosmetic kit for permanently reshaping the hair comprising:

a first compartment containing a pre-treating composition comprising, in a cosmetically acceptable medium, at least one entity chosen from non reducing inorganic acids, non reducing organic acids, and salts thereof, wherein the pH value of said pre-treating composition ranges from 2 to 5,

a second compartment containing a treating composition comprising, in a cosmetically acceptable medium, at least one hydroxide compound, and

optionally, a third compartment containing a post-treating composition comprising, in a cosmetically acceptable medium, at least one entity selected from inorganic acids, organic acids, and salts thereof.