Hair dyeing composition comprising an oxidation dye, a scleroglucan gum and an alkaline agent such as an amino acid
11278487 · 2022-03-22
Assignee
Inventors
- Sabrina Muller (Saint-Ouen, FR)
- Delphine Charrier (Saint-Ouen, FR)
- Mladen Milic (Saint-Ouen, FR)
- Laurie Biancucci (Saint-Ouen, FR)
- Cindy Yadel (Saint-Ouen, FR)
Cpc classification
A61K2800/4324
HUMAN NECESSITIES
A61K8/44
HUMAN NECESSITIES
A61K8/84
HUMAN NECESSITIES
A61K8/411
HUMAN NECESSITIES
A61K8/4946
HUMAN NECESSITIES
International classification
A61K8/44
HUMAN NECESSITIES
A61K8/84
HUMAN NECESSITIES
Abstract
The disclosure relates to a composition for dyeing keratin fibers, in particular human keratin fibers such as hair, comprising one or more oxidation dyes, one or more scleroglucan gums in a total weight content greater than or equal to 0.5% relative to the total weight of the composition, one or more alkaline agents selected from amino acids, the amino acid(s) being present in a total weight content greater than or equal to 1% relative to the weight of the composition, and preferably one or more additional alkaline agents, preferably selected among the mineral alkaline agents and/or alcanolamines. A method for dyeing keratin fibers using said composition and a multi-compartment device suitable for implementing said composition are also disclosed.
Claims
1. A composition for dyeing keratin fibers, comprising: at least one oxidation dye; at least one scleroglucan gum present in a total amount of greater than or equal to 0.5% by weight, relative to the total weight of the composition; and at least one alkaline agent chosen from amino acids, wherein the at least one alkaline agent chosen from amino acids is present in a total amount of greater than or equal to 1% by weight, relative to the weight of the composition.
2. The composition of claim 1, wherein the at least one scleroglucan gum is present in an amount ranging from 0.5% to 10% by weight, relative to the total weight of the composition.
3. The composition of claim 1, wherein the at least one oxidation dye is chosen from benzene-based oxidation bases, or salts thereof; wherein the at least one oxidation dye is optionally combined with at least one coupler chosen from meta-phenylenediamines, meta-aminophenols, meta-diphenols, naphthalene-based couplers, heterocyclic couplers, salts thereof, or mixtures thereof.
4. The composition of claim 1, wherein the at least one oxidation dye is chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols, heterocyclic bases, salts thereof, or mixtures thereof.
5. The composition of claim 1, wherein the at least one alkaline agent chosen from amino acids is present in a total amount ranging from 1% to 10% by weight, relative to the total weight of the composition.
6. The composition of claim 1, wherein the at least one alkaline agent chosen from amino acids is chosen from aspartic acid, glutamic acid, alanine, arginine, ornithine, citrulline, asparagine, carnitine, cysteine, glutamine, glycine, histidine, lysine, isoleucine, leucine, methionine, N-phenylalanine, proline, serine, taurine, threonine, tryptophan, tyrosine, valine, or mixtures thereof.
7. The composition of claim 1, wherein the at least one alkaline agent chosen from amino acids is chosen from basic amino acids.
8. The composition of claim 1, further comprising at least one additional alkaline agent chosen from mineral alkaline agents and/or alkanolamines.
9. The composition of claim 7, wherein the at least one additional alkaline agent chosen from alkanolamines is chosen from monoalkanolamines, dialkanolamines, trialkanolamines, or mixtures thereof, comprising one to three identical or different C.sub.1 to C.sub.4 hydroxyalkyl radicals.
10. The composition of claim 9, wherein the at least one additional alkaline agent chosen from alkanolamines is chosen from monoethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, N,N-dimethylethanolamine, 2-amino-2-methyl-1-propanol, triisopropanolamine, 2-amino-2-methyl-1,3-propanediol, 3-amino-1,2-propanediol, 3-dimethylamino-1,2-propanediol, tris(hydroxymethyl)aminomethane, or mixtures thereof.
11. The composition of claim 1, further comprising at least one cationic surfactant chosen from cetyltrimethylammonium salts, behenyltrimethylammonium salts, dipalmitoylethylhydroxyethylmethylammonium salts, or mixtures thereof.
12. The composition of claim 1, further comprising at least one nonionic surfactant chosen from: saturated or unsaturated, linear or branched, oxyethylenated fatty alcohols including at least one C.sub.8 to C.sub.40 alkyl chain, and comprising from 1 to 100 mol of ethylene oxide; alkyl(poly)glycosides; or mixtures thereof.
13. The composition of claim 1, further comprising at least one associative polymer present in a total amount ranging from 0.01% to 10% by weight, relative to the total weight of the composition.
14. The composition of claim 13, wherein the at least one associative polymer is nonionic, and is chosen from celluloses modified with groups including at least one fatty chain.
15. The composition of claim 1, further comprising at least one cationic polymer chosen from: (1) dialkyldiallylammonium homopolymers; and/or (2) cationic polymers that are constituted of repeating units corresponding to formula (IV): ##STR00004## wherein in formula (IV), R.sub.1, R.sub.2, R.sub.3, and R.sub.4, which may be identical or different, are chosen from an alkyl or hydroxyalkyl radical containing from 1 to 4 carbon atoms, n and p are integers ranging from 2 to 20, and X- is an anion derived from a mineral or organic acid.
16. The composition of claim 1, further comprising at east one carboxylic acid chosen from oxalic acid, malonic acid, malic acid, glutaric acid, citraconic acid, citric acid, maleic acid, succinic acid, adipic acid, tartaric acid, fumaric acid, or mixtures thereof.
17. The composition of claim 1, further comprising at least one chemical oxidizing agent.
18. The composition of claim 17, wherein the at least one chemical oxidizing agent is chosen from hydrogen peroxide and/or at least one system generating hydrogen peroxide.
19. A method for dyeing keratin fibers comprising: applying to the keratin fibers a dye composition (A) and an oxidizing composition (B); wherein the dye composition (A) comprises: at least one oxidation dye; at least one scleroglucan gum present in a total amount of greater than or equal to 0.5% by weight, relative to the total weight of the dye composition (A); and at least one alkaline agent chosen from amino acids. wherein the at least one alkaline agent chosen from amino acids is present in a total amount of greater than or equal to 1% by weight, relative to the weight of the dye composition (A); wherein the oxidizing composition (B) comprises at least one chemical oxidizing agent; and wherein the oxidizing composition (B) is extemporaneously mixed with the dye composition (A) just before being applied to the keratin fibers, or alternatively, the dye composition (A) and the oxidizing composition (B) are applied sequentially to the keratin fibers without intermediate rinsing.
20. The method of claim 19, wherein the at least one chemical oxidizing agent is chosen from hydrogen peroxide and/or at least one system generating hydrogen peroxide.
Description
EXAMPLE 1
(1) The following compositions were prepared from the following ingredients in the following proportions indicated in grams:
(2) TABLE-US-00001 Comparative Composition A2 composition according to the A1 invention Ammonium hydroxide 1.23 1.23 Arginine 0.5 3 Ethanolamine 5 5 EDTA 0.2 0.2 Sodium sulfite 0.5 0.5 Citric acid 3.3 3.3 Sodium metasilicate 2 2 Toluene-2,5-diamine 0.16 0.16 4-Amino-2-hydroxytoluene 0.92 0.92 5-Amino-6-chloro-o-cresol 0.2 0.2 1-Hydroxyethyl 4,5-diaminopyrazole 1.44 1.44 sulfate p-Aminophenol 0.12 0.12 Fragance qs qs Polyquaternium-11 1.84 1.84 Hexadimethrine chloride 1.2 1.2 Polyquaternium-6 0.8 0.8 Cetylhydroxyethylcellulose 0.2 0.2 Sclerotium gum 1 1 Water qs 100 qs 100 Glycerol 10 10 Cetrimonium chloride 0.25 0.25 Caprylyl/capryl glucoside 0.6 0.6 Ascorbic acid 0.4 0.4
(3) Visual Evaluation of the Stability of the Compositions
(4) The stability of the dye compositions was evaluated by observing them at T0 and then after 48 h at room temperature (25° C.) and then after 2 months of storage at 45° C.
(5) TABLE-US-00002 Composition A1 Composition A2 Observation at T0 (immediately Translucent gel Translucent gel after preparation) at room Homogeneous (no Homogeneous(no temperature (25° C.) phase separation) phase separation) Observation after 2 months at Translucent gel Translucent gel 45° C. Homogeneous (no Homogeneous (no phase separation) phase separation)
(6) It is observed that composition A1 (comparative) and composition A2 according to the invention are homogeneous and form a translucent gel at T0. After 2 months at 45° C., compositions A1 and A2 according to the invention are stable and in gel form; they are homogeneous and translucent. Comparative composition C5 in which the scleroglucan gum has been replaced weight-for-weight with another thickener, hydroxypropylcellulose, is not stable, and is liquid. Thus, it is not homogeneous; phase separation of these compositions is observed as early as T0.
EXAMPLE 2
(7) Compositions A1 and A2 of example 1 were mixed with 1 times their weight of 20-volumes oxidizing agent (6 g % of H2O2 AM); the mixture thus obtained was applied to locks of natural hair containing 90% white hairs.
(8) The “mixture/lock” bath ratio is, respectively, 10/1 (g/g).
(9) The leave-on time is 30 minutes, on a hotplate set at 27° C. On conclusion of the leave-on time, the locks are rinsed and then dried under a drying hood at 40° C.
(10) The color of the locks was evaluated in the CIE L* a* b* system, using a Minolta CM3600D spectrocolorimeter
(11) TABLE-US-00003 a* b* C* Coloring obtained with the 18.32 8.12 20.04 mixture of composition A1 + oxidizing agent (outside the invention) Coloring obtained with the 21.40 10.03 23.63 mixture of composition A2 + oxidizing agent (according to the invention)
(12) The mixture obtained using composition A2 according to the invention gives a higher C* value, and thus better chromaticity than the mixture obtained using the comparative composition A1.