WO2017185227A1 - Composition for treating keratin fibers - Google Patents

Composition for treating keratin fibers Download PDF

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Publication number
WO2017185227A1
WO2017185227A1 PCT/CN2016/080201 CN2016080201W WO2017185227A1 WO 2017185227 A1 WO2017185227 A1 WO 2017185227A1 CN 2016080201 W CN2016080201 W CN 2016080201W WO 2017185227 A1 WO2017185227 A1 WO 2017185227A1
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Prior art keywords
composition
weight
oil
alkyl
mixture
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PCT/CN2016/080201
Other languages
French (fr)
Inventor
Yixi ZHOU
Haidong JIA
Chensu XU
Original Assignee
L'oreal
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Application filed by L'oreal filed Critical L'oreal
Priority to CN201680085008.XA priority Critical patent/CN109475486A/en
Priority to PCT/CN2016/080201 priority patent/WO2017185227A1/en
Publication of WO2017185227A1 publication Critical patent/WO2017185227A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/31Hydrocarbons
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/463Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/602Glycosides, e.g. rutin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/604Alkylpolyglycosides; Derivatives thereof, e.g. esters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/645Proteins of vegetable origin; Derivatives or degradation products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/731Cellulose; Quaternized cellulose derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/30Characterized by the absence of a particular group of ingredients
    • A61K2800/34Free of silicones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/596Mixtures of surface active compounds

Definitions

  • the present invention relates to hair care cosmetic field, more specifically, it relates to new compositions having improved anti-particle deposition and good conditioning effect to keratin fibers, and meanwhile possessing a transparent esthetic property.
  • Air pollution for example the airborne dust particles, becomes a severe public concern, poses threat to the human health, and attracts consumers attention for the impact on keratin fibers, in particular the hair.
  • the human hair is damaged or weakened by the chemical action of environmental agents and/or of hair treatments such as permanent-waving, dyeing or bleaching. In particular, being exposed to the air, hair is damaged and weakened by air pollution.
  • the term “PM 2.5 (PM 10) ” also knowns as particulate matters, or fine particles, refers to particles which pass through a size-selective inlet with a 50%efficiency cut-off at 2.5 ⁇ m (10 ⁇ m for PM 10) aerodynamic diameter, as defined in ISO 7708: 1995, 7.1.
  • the particulate matters are understood as a complex mixture comprising small particles and liquid droplets, which float in the air. Fine particles existing in the air tend to be adherent to the hair. They will deposit on the hair and stay even after washing. This deposition makes the hair dirty, lank, and greasy.
  • Moringa oleifera seed extract is known for its use in hair care cosmetic compositions. In particular, it is used in anti-pollution hair care products. For example, shampoos containing surfactants, Moringa oleifera seed extract, and various types of conditioning agents are known.
  • esthetic appearance of a cosmetic product plays an important role in attracting the interests of consumers.
  • Products, especially products used for cleansing, washing, or deterging, are often favored by the consumers when they are transparent or transparent, thanks to the light, fresh, and clean feeling generated by the transparency or translucency appearance.
  • compositions mentioned above satisfies all the needs mentioned above, in particular regarding the balance between a good conditioning of the hair, as well as an improved anti-particle deposition effect, meanwhile maintaining a transparent appearance. This is to say, it is difficult to formulate a transparent composition with an improved anti-particle deposition effect, and a good conditioning effect.
  • the present invention is directed towards meeting these needs.
  • a transparent composition for treating keratin fibers comprising at least one surfactant of anionic, amphoteric or zwitterionic type, at least one nonionic surfactant, at least one protein extract of moringa genus plant seeds, at least one cationic polymer selected from cationic cellulose, and at least one hydrocarbon-based oil.
  • the term “transparent” is understood to mean a composition having a turbidity of less than 250 NTU (Nephelometric Turbidity Units) at 25°C and preferably of less than 150 NTU at 25°C, even more preferably less than 100 NTU at 25°C, measured with a 2100N Turbidimeter machine from HACH, wherein the sample cells for turbidity testing are made of quartz glass with reference Cat. 2084900.
  • NTU Nephelometric Turbidity Units
  • the composition of the present invention is silicone-free.
  • silicone or “silicone oil” is understood to mean any compound comprising at least one silicon atom, and preferably comprising Si-O groups.
  • silicone-free means the composition of the present invention comprising no silicone or silicone oil, or comprising silicone in an amount no more than 1%by weight of silicones relative to the total composition.
  • the composition may contain no more than 0.5%by weight, more preferably no more than 0.2%by weight, of silicones relative to the total weight of the composition.
  • composition of the present invention does not contain silicone.
  • the composition of the present invention is a rinse-off hair shampoo.
  • the “keratin fiber” according to the present invention is the hair.
  • anti-particle deposition refers to the reduction of particle deposition on keratin fibers, in particular hair.
  • the particle refers to the fine particles existing in the air.
  • Another aspect of the invention is a process for washing keratin fibers, especially the hair, comprising the steps of applying to said fibers the composition of the invention, and then washing with water after an optional period of exposure.
  • One aspect of the present invention is the use of the composition as defined above in reducing the deposition of fine particles contained in the air on keratin fibers, in particular the hair.
  • the terms “at least a” or “at least one” are equivalent to “one or more” .
  • composition according to the invention comprises at least one surfactant (or surface active agent) , selected from the group consisting of anionic surfactant, amphoteric or zwitterionic surfactant, or a mixture thereof.
  • surfactant or surface active agent
  • the composition of the present invention comprises a mixture of anionic surfactant (s) and amphoteric or zwitterionic surfactant (s) .
  • the surfactant of this type is present in an amount ranging from 1%to 70%by weight, preferably from 3%to 50%by weight, more preferably from 5%to 20%by weight, relative to the total weight of the composition.
  • anionic surfactant is understood to mean an amphiphilic compound with a hydrophobic part and a hydrophilic part wherein the hydrophilic part carries as ionic or ionisable group only anionic group with a cationic counterion which is generally metallic (alkali metal, such as Na or K) or ammonium, capable of dissociating to give anions in aqueous solution.
  • the cationic counter anion being usually selected from alkali metal such as sodium, or alkaline earth metal such as magnesium, or organic cationic counter anion such as ammonium salts, amine salts, or aminoalcohol salts.
  • the surfactants may also occur in their acid forms.
  • anionic surfactants of surfactants comprising carboxylate, sulfate, sulfonate, sulfoacetate, sulfosuccinate, phosphate, isethionate, sarcosinate, glutamate, lactylate or taurate anionic groups, salts of fatty acids, salts of galactosiduronic acids, salts of ether carboxylic acids surfactants and their mixtures.
  • anionic surfactant according to the invention is chosen from:
  • the anionic surfactant is chosen from sulfate of ether of lauryl alcohol and alkylene oxide containing from 1 to 4 alkylene oxide groups, especially ethylene oxide groups.
  • sulfate of ether of lauryl alcohol and alkylene oxide containing from 1 to 4 alkylene oxide groups, especially ethylene oxide groups.
  • alkylene oxide containing from 1 to 4 alkylene oxide groups especially ethylene oxide groups.
  • sodium laureth sulfate containing in average 2.2 ethylene oxide groups that are sold by the company Cognis (BASF) under the name AOS 225 UP, Rhodia under the name esb-70/fla3, Clariant under the name LRO L’O
  • sodium laureth sulfate containing in average 1 ethylene oxide group that is sold by the company Zhejiang Zanyu Technology under the name SLES (N1EO) .
  • acyl isethionates for example sodium lauroyl methyl isethionate, sodium cocoyl isthionate; mentiones may be made of the sodium lauroyl methyl isethionate which is sold under the trade name LQ-CLR-SB by the company Innospec Active Chemicals;
  • alkyl or acyl radicals of these various anionic surfactants preferably comprise from 12 to 20 carbon atoms.
  • the oxyalkylenated or polyoxyalkylenated anionic surfactants preferably comprise from 1 to 50 alkylene oxide groups, more preferably from 1 to 4 alkylene oxide groups, in particular ethylene oxide groups.
  • the present invention comprises at least one anionic surfactant chosen from (C 6 -C 30 ) alkyl sulfates, (C 6 -C 30 ) alkyl ether sulfates, (C 6 -C 30 ) alkylamido ether sulfates, alkylaryl polyether sulfates, monoglyceride sulfates, (C 6 -C 24 ) acyl isethionates, or a mixture thereof.
  • anionic surfactant chosen from (C 6 -C 30 ) alkyl sulfates, (C 6 -C 30 ) alkyl ether sulfates, (C 6 -C 30 ) alkylamido ether sulfates, alkylaryl polyether sulfates, monoglyceride sulfates, (C 6 -C 24 ) acyl isethionates, or a mixture thereof.
  • the anionic surfactant is preferably chosen from sodium laureth sulfate, sodium lauroyl methyl isethionate, sodium cocoyl isethionate, or a mixture thereof.
  • the anionic surfactant is sodium laureth sulfate containing in average 2.2 ethylene oxide groups.
  • the content of anionic surfactant (s) represents from 1%to 70%by weight, preferably from 2%to 40%by weight, more preferably from 5%to 20%by weight, with respect to the weight of the composition.
  • amphoteric or zwitterionic surfactant (s) that may be used in the present invention may be quaternized secondary or tertiary aliphatic amine derivatives containing at least one anionic group, for instance a carboxylate, sulfonate, sulfate, phosphate or phosphonate group, and in which the aliphatic group or at least one of the aliphatic groups is a linear or branched chain comprising from 8 to 22 carbon atoms.
  • alkylbetaine examples include behenylbetaine, cetyl betaine, cocoylbetaine, decylbetaine. From alkylbetaines, cocoylbetaine is preferred, for example the products sold by the company Rhodia under the tradename BB/FLA.
  • R a represents a C 10 -C 30 alkyl or alkenyl group derived from an acid R a -COOH preferably present in hydrolysed coconut oil, a heptyl group, a nonyl group or an undecyl group,
  • R b represents a ⁇ -hydroxyethyl group
  • R c represents a carboxymethyl group
  • n 0, 1 or 2
  • Z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group
  • B represents -CH 2 CH 2 OX', with X'representing -CH 2 -COOH, CH 2 -COOZ’, -CH 2 CH 2 -COOH, -CH 2 CH 2 -COOZ’, or a hydrogen atom,
  • Z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group
  • Z’ represents an ion resulting from an alkali or alkaline-earth metal, such as sodium, potassium or magnesium; an ammonium ion; or an ion resulting from an organic amine and in particular from an amino alcohol, such as monoethanolamine, diethanolamine and triethanolamine, monoisopropanolamine, diisopropanolamine or triisopropanolamine, 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1, 3-propanediol and tris (hydroxymethyl) aminomethane,
  • an alkali or alkaline-earth metal such as sodium, potassium or magnesium
  • an ammonium ion or an ion resulting from an organic amine and in particular from an amino alcohol, such as monoethanolamine, diethanolamine and triethanolamine, monoisopropanolamine, diisopropanolamine or triisopropanolamine, 2-amino-2-methyl-1-propanol, 2-amino-2-
  • R a' represents a C 10 -C 30 alkyl or alkenyl group of an acid R a' COOH preferably present in hydrolysed linseed oil or coconut oil, an alkyl group, in particular a C 17 alkyl group, and its iso form, or an unsaturated C 17 group.
  • cocamidopropyl betaine for example the product sold under the tradename Dehyton PK 45 by Cognis (BASF) .
  • R a represents a C 10 -C 30 alkyl or alkenyl group of an acid R a” -C (O) OH preferably present in hydrolysed linseed oil or coconut oil;
  • - Y'’ represents the group –C (O) OH, -C (O) OZ” , -CH 2 -CH (OH) -SO 3 H or the group -CH 2 -CH (OH) -SO 3 -Z” , with Z” representing a cationic counterion resulting from an alkali metal or alkaline-earth metal, such as sodium, an ammonium ion or an ion resulting from an organic amine;
  • R d and R e represent, independently of each other, a C 1 -C 4 alkyl or hydroxyalkyl radical
  • n denote, independently of each other, an integer ranging from 1 to 3.
  • amphoteric surfactants are chosen from (C 8 -C 20 ) alkylbetaines, (C 8 -C 20 ) alkylamido (C 1 -C 6 ) alkylbetaines, and mixtures thereof.
  • amphoteric or zwitterionic surfactant is chosen from cocamidopropyl betaine, cocoylbetaine, or a mixture thereof.
  • amphoteric or zwitterionic surfactant (s) is present in an amount ranging from 1%to 70%by weight, preferably from 3%to 50%by weight, more preferably from 5%to 15%by weight, relative to the total weight of the composition.
  • the composition comprises at least one nonionic surfactant selected from the group consisting of alkyl (poly) glycosides, fatty acid esters of glycerol and of polyglycerol, or a mixture thereof.
  • the composition comprises a mixture of nonionic surfactants of alkyl (poly) glycoside and fatty acid esters of glycerol and of polyglycerol.
  • alkyl (poly) glycoside denotes an alkylpolyglycoside or an alkylmonoglycoside, also referred to in the present patent application as an alkylglycoside, which may be alkoxylated with one or more alkylene oxide groups, preferentially of C 2 -C 4 .
  • alkyl (poly) glycoside nonionic surfactant (s) used, alone or as mixtures, in accordance with the present invention may be represented by formula (IV) below:
  • R 1 represents a linear or branched, saturated or unsaturated alkyl group, containing from about 8 to 24 carbon atoms, or an alkyl phenyl group in which the linear or branched alkyl radical contains from 8 to 24 carbon atoms,
  • R 2 represents an alkylene group containing from about 2 to 4 carbon atoms
  • G represents a saccharide unit containing 5 or 6 carbon atoms
  • t denotes a value ranging from 0 to 10 and preferably from 0 to 4, and
  • v denotes a value ranging from 1 to 15.
  • alkyl (poly) glycoside nonionic surfactant (s) correspond to formula (IV) in which:
  • R 1 denotes a linear or branched, saturated or unsaturated alkyl group containing from 8 to 18 carbon atoms
  • G denotes glucose, fructose or galactose, preferably glucose
  • t denotes a value ranging from 0 to 3, and is preferably equal to 0,
  • R 2 and v are as defined previously.
  • the degree of polymerization of the alkyl (poly) glycoside nonionic surfactant (s) as represented, for example, by the index v in formula (IV) ranges on average from 1 to 15 and preferably from 1 to 4. This degree of polymerization more particularly ranges from 1 to 2 and better still from 1.1 to 1.5, on average.
  • glycoside bonds between the saccharide units are 1, 6-or 1, 4-bonds; preferably 1, 4-bonds.
  • the compounds of formula (IV) that may be used in the present invention are especially represented by the products sold by the company Cognis under the names (600 CS/U, 1200 and 2000) or (818, 1200 and 2000) . It is also possible to use the products sold by the company SEPPIC under the names Triton CG 110 (or Oramix CG 110) and Triton CG 312 (or NS 10) , the products sold by the company BASF under the name Lutensol GD 70, or those sold by the company Chem Y under the name AG10 LK.
  • decyl glucoside sold by Cognis under the reference 2000 UP is preferably used.
  • the composition may comprise at least one fatty acid ester of glycerol and/or of polyglycerol.
  • the fatty acid ester (s) of polyglycerol is (are) chosen from esters resulting from the reaction of polyglycerol comprising from 2 to 12 glycerol units, preferably from 3 to 10 glycerol units, and of at least one fatty acid containing from 8 to 24 carbon atoms, preferably from 8 to 22 carbon atoms, better still from 10 to 20 carbon atoms and even better still from 10 to 18 carbon atoms.
  • the fatty acids containing from 8 to 24 carbon atoms may be linear or branched, and saturated or unsaturated.
  • the fatty acids may be chosen from oleic acid, stearic acid, isostearic acid, lauric acid, palmitic acid, myristic acid, linoleic acid, capric acid and caprylic acid, or mixtures thereof.
  • the fatty acid esters of polyglycerol can be chosen from monoesters, diesters, triesters and tetraesters, polyesters and mixtures thereof. Use is preferably made of esters with a low degree of esterification, for instance fatty acid monoesters, diesters or triesters of polyglycerol, or a mixture.
  • the fatty acid ester of polyglycerol can be in the form of a mixture of esters with a low degree of esterification, for instance a mixture of monoester and diester or a mixture of monoester, diester and triester.
  • the fatty acid ester of polyglycerol is chosen from esters resulting from the reaction of polyglycerol comprising from 3 to 10 glycerol units and of at least one fatty acid containing from 8 to 20 carbon atoms, preferably from 10 to 18 carbon atoms, such as oleic acid or linoleic acid.
  • polyglyceryl-2 distearate in particular as sold by NIHON EMULSION under the name Emalex PGSA
  • polyglyceryl-10 decastearate in particular as sold by TAIYO KAGAKU under the name Sunsoft Q-1810S
  • glyceryl oleate in particular as sold by COGNIS under the name Monomuls 90-O 18
  • glyceryl stearate in particular as sold by COGNIS under the name Cutina GMS V
  • polyglyceryl-5 hexastearate in particular as sold by TAIYO KAGAKU under the name Sunsoft A-186E
  • polyglyceryl-10 pentaoleate in particular as sold by TAIYO KAGAKU under the name Sunsoft Q-175S
  • polyglyceryl-10 pentastearate in particular as sold by TAIYO KAGAKU under the name Sunsoft Q-185S
  • glyceryl caprylate/caprate in particular as
  • the fatty acid which is suitable for the reaction with the ester (s) of polyglycerol comprises at least one hydroxyl group.
  • the fatty acid which is suitable for the reaction with the ester (s) of polyglycerol is a polyacid comprising at least one hydroxyl group.
  • the nonionic surfactant (s) is (are) present in the composition ranging from 0.05%to 20%by weight, preferably from 0.1%to 10%by weight, more preferably 0.5%to 5%by weight, relative to the total weight of the composition.
  • composition according to the present invention comprises at least one protein extract of Moringa genus plant seeds.
  • the genus Moringa comprises some 14 species of plants (of which particularly Moringa peregrina, M. aptera, M concane six, M. drouhardii, M. hildebrandtit', M. longituba) , among which Moringa pterygosperma (synonym: Moringa oleifera) is the best known.
  • the seeds of Moringa are characterized by the presence of an oil whose content varies between 21 and 53%according to the species and maturity of the seeds.
  • Moringa seeds are found to comprise compounds of proteic nature (see particularly the article “Isolation and characterization of a flocculating protein from Moringa oleifera lam” by U. Gassenschmidt, K.D. Jany, B. Tausche and H.R. Niebergall, Biochimica and biophysics acta, 1243: 477-481, 1995- “Active agents and mechanism of coagulation of turbid waters using Moringa oleifera” , of A. Ndabigengesere, K. Subba Narasiah and B.G. Talbot, Water research, 29, 2: 703-710, 1995) .
  • the composition of the present invention comprises at least one protein extract of the seeds of Moringa oleifera.
  • the extract is preferably obtained from delipidated flour of Moringa oleifera seeds, and was then extracted in a buffered aqueous medium, and then isolated by cation exchange chromatography.
  • the protein extract is obtained in an aqueous medium with a pH of greater than or equal to 3, preferably from 3 to 8.
  • the protein extract according to the present invention is also disclosed, for example, in the patent application US 6,500,470 B1.
  • Mentions maybe made of commercially available products, such as those sold under the name Purisoft POE LS 9726 by the company BASF.
  • the protein extract of Moringa genus plant seeds is present in the composition in an amount ranging from 0.001%to 5%by weight, preferably from 0.001%to 2%by weight, relative to the total weight of the composition.
  • composition of the present invention comprises at least one cationic polymer selected from cationic cellulose.
  • cationic polymer denotes any polymer containing cationic groups and/or groups that can be ionized into cationic groups.
  • the cationic polymers that may be used preferably have a weight-average molar mass (Mw) of between 500 and 5 ⁇ 10 6 approximately and preferably between 103 and 3 ⁇ 10 6 approximately.
  • the cationic celluloses may be made more particularly chosen from cellulose ether derivatives comprising quaternary ammonium groups, cationic cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer, or a mixture thereof.
  • the cellulose ether derivatives comprising quaternary ammonium groups are especially described in French patent 1 492 597, and mention may be made of the polymers (INCI name polyquaternium-10) sold under the name Ucare Polymer “JR” (JR 400 LT, JR 125 and JR 30M) or “LR” (LR 400 or LR 30M) by the company Amerchol. These polymers are also defined in the CTFA dictionary as quaternary ammoniums of hydroxyethylcellulose that have reacted with an epoxide substituted with a trimethylammonium group.
  • Cationic cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer are described especially in US patent 4 131 576, and mention may be made of hydroxyalkylcelluloses, for instance hydroxymethyl-, hydroxyethyl-or hydroxypropylcelluloses grafted, in particular, with a methacryloylethyltrimethylammonium, methacrylamidopropyltrimethylammonium or dimethyldiallylammonium salt.
  • the commercial products corresponding to this definition are more particularly the products sold under the names Celquat L 200 and Celquat H 100 by the company National Starch.
  • the cationic cellulose of the present invention is chosen from cellulose ether derivatives, more particularly comprising quaternary ammonium groups.
  • the cationic polymer is present in the composition of the present invention, ranging from 0.01%to 3%by weight, preferably from 0.05%to 2%by weight, more preferably 0.1%to 1.5%by weight, relative to the total weight of the composition.
  • composition of the present invention comprises at least one hydrocarbon-based oil.
  • oil means any nonionic lipophilic compound that is insoluble in water and liquid at room temperature (25°C) and at atmospheric pressure.
  • water-insoluble refers to a compound whose solubility at spontaneous pH in water at 25°C and at atmospheric pressure is less than 1%and preferably less than 0.5%.
  • the oils preferably have a melting point of less than 5°C and a viscosity of less than 500 cPs at 25°C at a shear rate of 1 s -1 .
  • hydrocarbon-based oil is understood to mean oil essentially formed and even composed, of carbon and hydrogen atoms and optionally of oxygen and nitrogen atoms which does not comprise a silicone or fluorine atom; it can comprise ester, ether, amine and amide groups.
  • the oil may be volatile or non-volatile.
  • non-volatile means an oil of which the vapor pressure at 25°C and atmospheric pressure is non-zero and is less than 0.02 mmHg (2.66 Pa) and better still less than 10-3 mmHg (0.13 Pa) .
  • volatile oil means an oil of which the vapor pressure at 25°C and atmospheric pressure is from 0, 13 Pa to 40.000 Pa (0, 001 to 300 mmHg) and preferably from 1, 3 to 1300 Pa (0, 01 to 10 mm Hg) .
  • the composition of the present invention comprises at least one oil selected from the group consisting of plant oil, hydrocarbon oil, or a mixture thereof.
  • plant oil means an oil as defined above, obtained from a species belonging to the plant kingdom.
  • Hydrocarbon oils are also referred to as mineral oils.
  • the term “hydrocarbon oils” or “mineral oils” refers to complex substances of hydrocarbons in the form of linear, branched, or cyclic, saturated or unsaturated oils. These oils are obtained from crude petroleum oils by distillation and refining. Hydrocarbon oils, or mineral oils are a complex of alkanes, cycloalkanes, aromatic hydrocarbons, or mixtures thereof. More preferably the hydrocarbon oils contain a chain with 15-40 carbon atoms.
  • hydrocarbon oils or mineral oils examples include:
  • isoparaffins such as isohexadecane, isododecane and hydrogenated polyisobutylenes such as oil sold by the company NOF Corporation (INCI name: Hydrogenated polyisobutene) .
  • polydecenes means any compound of formula C 10n H (20n) +2 in which n ranges from 3 to 9, corresponding to the name “polydecene” in the CTFA dictionary, 7th edition, 1997 of the Cosmetic, Toiletry and Fragrance Association, USA, and also to the same INCI name in the USA and in Europe. These are poly-1-decene hydrogenation products. Among these compounds, those for which, in the formula, n ranges from 3 to 7 are more particularly chosen according to the invention.
  • Examples that may be mentioned include the products sold under the name 366 NF Polydecene by the company Amoco Chemical, and those sold under the names 2002 FG, 2004 FG, 2006 FG and 2008 FG by the company Fortum.
  • the preferred hydrocarbon oil is mixtures of hydrocarbon-based oils derived from petroleum (INCI name: Mineral Oil) , volatile or non-volatile liquid paraffin, or a mixture thereof.
  • Mentions may be made of the product (INCI name: mineral oil) sold under the tradename Emcaplus 70 by the company Oxiteno.
  • the composition of the present invention comprises at least one hydrocarbon oil.
  • the total amount of oil (s) when they are present in the composition, preferably ranges from 0.01%to 20%by weight, better still from 0.05%to 10%by weight and more particularly from 0.1%to 5%by weight relative to the total weight of the final composition.
  • the present invention relates to a composition for treating keratin fibers, comprising, by weight relative to the total weight of the composition:
  • At least one nonionic surfactant selected from alkyl (poly) glycosides, fatty acid esters of glycerol and of polyglycerol, or a mixture thereof;
  • composition according to the invention may take the form of thickened liquid, creams or gel. It is preferable that the composition according to the present invention be in the form of an nano-or micro-emulsion, more particularly oil-in-water nano-or micro-emulsion.
  • phase inversion temperature (PIT emulsions) in which the average size of the globules constituting the oily phase is within given limits, namely between 0.1 and 4 ⁇ m (100 to 4000 nm) .
  • PIT emulsions phase inversion temperature technique
  • the principle of phase inversion temperature (or PIT) emulsification is, in theoretical terms, well known to those skilled in the art; it was described in 1968 by K. Shinoda (J. Chem. Soc. Jpn., 1968, 89, 435) . It was shown that this emulsification technique makes it possible to obtain stable fine emulsions (K. Shinoda and H. Saito, J. Interface Sci., 1969, 30, 258) .
  • compositions according to the invention may naturally contain, in addition, all the standard adjuvants encountered in the field of shampoos, such as, for example, perfumes, preservatives, sequestering agents, thickeners, hydrating agents, anti-dandruff or antiseborrhoeic agents, vitamins, sunscreen agents, suspending agents and the like.
  • standard adjuvants encountered in the field of shampoos such as, for example, perfumes, preservatives, sequestering agents, thickeners, hydrating agents, anti-dandruff or antiseborrhoeic agents, vitamins, sunscreen agents, suspending agents and the like.
  • the present invention also relates to a process for washing keratin fibers, especially the hair, comprising the steps of applying to said fibers the composition of the invention, and then washing with water after an optional period of exposure.
  • the process as mentioned above is preferably a process for washing and conditioning keratin fibers, in particular the hair.
  • Another aspect of the present invention is the use of the above composition of the invention for washing and conditioning keratin fibers, especially hair.
  • the present invention further relates to the use of the above composition in reducing the deposition of fine particles contained in the air on keratin fibers, in particular the hair.
  • Comparative formula A’ corresponds to the invention formula A and contains a polymer other than the one claimed in the present invention
  • Comparative formula B corresponds to the invention formula B and contains silicone oil instead of the oil as claimed in the present invention
  • Comparative formula B” also corresponds to the invention formula B and contains a nonionic surfactant other than the one claimed in the present invention.
  • the invention and comparative formulas were prepared according to the conventional methods for preparing shampoo formulations.
  • the ingredients listed above were mixed until homogeneous at room temperature (20-25°C) .
  • the invention and comparative formulas were subject to the evaluations, including the conditioning effect, anti-particle deposition effect, and transparency.
  • the transparency was evaluated by the turbidity, using a 2100N Turbidimeter machine from HACH.
  • the term “transparent” is understood to mean a composition having a turbidity of less than 250 NTU (Nephelometric Turbidity Units) at 25°C and preferably of less than 150 NTU at 25°C, even more preferably less than 100 NTU at 25°C.
  • the conditioning effect was evaluated by a hair dresser by using each of the invention or comparative formulas on 6 women consumers as hair shampoos, then combing the hair for 10 minutes. Finally the scores were given to the formulas, respectively:
  • the formula was considered to have an expected conditioning when the average score of the formula is greater than or equal to 2.5.
  • the carbon powders used in the evaluation were intended to simulate the fine particles or in particular PM 2.5 contained in the air.
  • the particle size of the carbon powder in aqueous solution when tested with Malvern Mastersizer 3000, distributed from 0.5 ⁇ m to 10 ⁇ m, which corresponds to the particle size of the fine particles in the air, including PM 2.5.
  • PM 2.5 comprises, but not limited to: geological materials such as paved or unpaved roads, constructions, agricultural operations, wind-blown soil; organic matters from cooking, residential heating, field burning of crop residue, forest fires, and grassland fires; organic carbon such as conversion of volatile organic compounds; ammonium, sulfates, nitrates, and fugitive dust, see in “Winter and Summer PM 2.5 Chemical Compositions in Fourteen Chinese Cities” Jun-ji CAO, etc., Journal of the Air and Waste Management Association, 24 th , Sep, 2012.
  • the swatch treated with invention formula and comparative formulas were placed in a chamber equipped with carbon powders, one fan, and one particle detector, by fixing one end of the hair swatch on a horizontally positioned shelf.
  • the fan was placed in the center of the chamber.
  • a watch glass with 0.1 g carbon black powder was placed under the fan, right in the center.
  • a particle detector (Dust Trak II Model 8532 sold by the company TSI) was placed in the chamber and finally the chamber of the device was closed.
  • the fan was then turned on for 10 minutes, and then turned off. After 5 minutes, the swatches were moved out from the chamber and observed under SEM.
  • the anti-particle deposition effect of the formulas was represented by particle deposition coverage value, obtained by image analyzing tools which are conventionally available.
  • invention formula A and B both have good conditioning effect on the hair, and both have improved anti-particle deposition effect, meanwhile are transparent. Whereas even though the conditioning effect is good, neither of the comparative formula B’or B” has a transparent esthetic appearance, and moreover, the anti-particle deposition effect is poor comparing to the invention formula B. Comparative formula A’possesses a transparent appearance, however it does not have a good balance of conditioning effect and anti-particle deposition effect, comparing to the invention formula A, i.e., both of which are worse than that of the invention formula A.

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Abstract

Provided is a transparent composition for treating keratin fiber, comprising at least one surfactant selected from the group consisting of anionic surfactants, amphoteric and/or zwitterionic surfactants, or a mixture thereof; at least one nonionic surfactant selected from the group consisting of alkyl(poly)glycosides, fatty acid esters of glycerol and of polyglycerol, or a mixture thereof; at least one protein extract of moringa genus plant seed; at least one cationic polymer chosen from cationic cellulose, and at least one hydrocarbon-based oil.

Description

COMPOSITION FOR TREATING KERATIN FIBERS FIELD OF THE INVENTION
The present invention relates to hair care cosmetic field, more specifically, it relates to new compositions having improved anti-particle deposition and good conditioning effect to keratin fibers, and meanwhile possessing a transparent esthetic property.
BACKGROUND OF THE INVENTION
Air pollution, for example the airborne dust particles, becomes a severe public concern, poses threat to the human health, and attracts consumers attention for the impact on keratin fibers, in particular the hair.
The human hair is damaged or weakened by the chemical action of environmental agents and/or of hair treatments such as permanent-waving, dyeing or bleaching. In particular, being exposed to the air, hair is damaged and weakened by air pollution.
Among different types of pollutants existing in the air, dust or fine particles such as PM 2.5, PM 10, carbon powders, gases such as CO, SO2, NOx, have been raising attentions of the consumers, in particular since recent years.
As used herein, the term “PM 2.5 (PM 10) ” , also knowns as particulate matters, or fine particles, refers to particles which pass through a size-selective inlet with a 50%efficiency cut-off at 2.5 μm (10 μm for PM 10) aerodynamic diameter, as defined in ISO 7708: 1995, 7.1. The particulate matters are understood as a complex mixture comprising small particles and liquid droplets, which float in the air. Fine particles existing in the air tend to be adherent to the hair. They will deposit on the hair and stay even after washing. This deposition makes the hair dirty, lank, and greasy.
It is known to the art to use active agents for preventing the deposition of pollutants on the hair, and thus reducing the hair dirty, greasy, and lank issue faced by the consumers.
Moringa oleifera seed extract is known for its use in hair care cosmetic compositions. In particular, it is used in anti-pollution hair care products. For example, shampoos containing surfactants, Moringa oleifera seed extract, and various types of conditioning agents are known.
On the other hand, esthetic appearance of a cosmetic product plays an important role in attracting the interests of consumers. Products, especially products used for cleansing, washing, or deterging, are often favored by the consumers when they are transparent or transparent, thanks to the light, fresh, and clean feeling generated by the transparency or translucency appearance.
None of the compositions mentioned above satisfies all the needs mentioned above, in particular regarding the balance between a good conditioning of the hair, as well as an improved anti-particle deposition effect, meanwhile maintaining a transparent appearance. This is to say, it is difficult to formulate a transparent composition with an improved anti-particle deposition effect, and a good conditioning effect.
There is thus a need for new products with esthetic appearance, displaying improved balance of the properties mentioned above.
In particular, there exists a need for formulating a transparent composition which provides to keratin fibers, in particular the hair, an improved balance between conditioning effect as well as anti particle deposition effect.
The present invention is directed towards meeting these needs.
BRIEF DESCRIPTION OF THE INVENTION
The aim of the present invention is achieved by a transparent composition for treating keratin fibers, comprising at least one surfactant of anionic, amphoteric or zwitterionic type, at least one nonionic surfactant, at least one protein extract of moringa genus plant seeds, at least one cationic polymer selected from cationic cellulose, and at least one hydrocarbon-based oil.
The term “transparent” is understood to mean a composition having a turbidity of less than 250 NTU (Nephelometric Turbidity Units) at 25℃ and preferably of less than 150 NTU at 25℃, even more preferably less than 100 NTU at 25℃, measured with a 2100N Turbidimeter machine from HACH, wherein the sample cells for turbidity testing are made of quartz glass with reference Cat. 2084900.
Preferably, the composition of the present invention is silicone-free.
As used herein, the term “silicone” or “silicone oil” is understood to mean any compound comprising at least one silicon atom, and preferably comprising Si-O groups.
As used herein, the term “silicone-free” means the composition of the present invention comprising no silicone or silicone oil, or comprising silicone in an amount no more than 1%by weight of silicones relative to the total composition.
Preferably, the composition may contain no more than 0.5%by weight, more preferably no more than 0.2%by weight, of silicones relative to the total weight of the composition.
More preferably, the composition of the present invention does not contain silicone.
Preferably, the composition of the present invention is a rinse-off hair shampoo.
Preferably, the “keratin fiber” according to the present invention is the hair.
The term “anti-particle deposition” as used herein refers to the reduction of particle  deposition on keratin fibers, in particular hair. The particle refers to the fine particles existing in the air.
Another aspect of the invention is a process for washing keratin fibers, especially the hair, comprising the steps of applying to said fibers the composition of the invention, and then washing with water after an optional period of exposure.
One aspect of the present invention is the use of the composition as defined above in reducing the deposition of fine particles contained in the air on keratin fibers, in particular the hair.
In the description, the terms “at least a” or “at least one” are equivalent to “one or more” .
Other characteristics and advantages of the invention will emerge more clearly on reading the description and the examples that follow.
DETAILED DESCRIPTION OF THE PRESENT INVENTION
Surfactant (s)
The composition according to the invention comprises at least one surfactant (or surface active agent) , selected from the group consisting of anionic surfactant, amphoteric or zwitterionic surfactant, or a mixture thereof.
According to an embodiment, the composition of the present invention comprises a mixture of anionic surfactant (s) and amphoteric or zwitterionic surfactant (s) .
According to an embodiment, the surfactant of this type is present in an amount ranging from 1%to 70%by weight, preferably from 3%to 50%by weight, more preferably from 5%to 20%by weight, relative to the total weight of the composition.
i) Anionic surfactant (s) 
The term “anionic surfactant” is understood to mean an amphiphilic compound with a hydrophobic part and a hydrophilic part wherein the hydrophilic part carries as ionic or ionisable group only anionic group with a cationic counterion which is generally metallic (alkali metal, such as Na or K) or ammonium, capable of dissociating to give anions in aqueous solution.
More particularly the anionic group of the anionic surfactant is belonging to the group chosen from: C (O) OH, –C (O) O-, -SO3H, -S (O) 2O-, -OS (O) 2OH, -OS (O) 2O-, -P (O) OH2, -P (O) 2O-, -P (O) O2 -, -P (OH) 2, =P (O) OH, -P (OH) O-, =P (O) O-, =POH, =PO-, the cationic counter anion being usually selected from alkali metal such as sodium, or alkaline earth metal such as magnesium, or organic cationic counter anion such as ammonium salts, amine salts, or aminoalcohol salts. The surfactants may also occur in their acid forms.
Mention may be made, as anionic surfactants, of surfactants comprising carboxylate,  sulfate, sulfonate, sulfoacetate, sulfosuccinate, phosphate, isethionate, sarcosinate, glutamate, lactylate or taurate anionic groups, salts of fatty acids, salts of galactosiduronic acids, salts of ether carboxylic acids surfactants and their mixtures.
More particularly, the anionic surfactant according to the invention is chosen from:
· (C6-C30) alkyl sulfates, (C6-C30) alkyl ether sulfates, (C6-C30) alkylamido ether sulfates, alkylaryl polyether sulfates or monoglyceride sulfates; preferably for this type of anionic surfactants, (C6-C30) alkyl ether sulfates, alkylaryl polyether sulfates, or a mixture is used. Mentions may be made of sulfate of ether of lauryl alcohol and alkylene oxide, containing from 1 to 50 alkylene oxide groups.
More preferably, the anionic surfactant is chosen from sulfate of ether of lauryl alcohol and alkylene oxide containing from 1 to 4 alkylene oxide groups, especially ethylene oxide groups. For example, sodium laureth sulfate containing in average 2.2 ethylene oxide groups that are sold by the company Cognis (BASF) under the nameAOS 225 UP, Rhodia under the name
Figure PCTCN2016080201-appb-000002
esb-70/fla3, Clariant under the name
Figure PCTCN2016080201-appb-000003
LRO L’O, and sodium laureth sulfate containing in average 1 ethylene oxide group that is sold by the company Zhejiang Zanyu Technology under the name SLES (N1EO) .
· (C6-C30) alkyl sulfonates, (C6-C30) alkylamidesulfonates, (C6-C30) alkylaryl sulfonates, α-olefin sulfonates, paraffin sulfonates;
· (C6-C30) akyl phosphates;
· (C6-C30) alkyl sulfosuccinates, (C6-C30) alkyl ether sulfosuccinates or (C6-C30) alkylamido sulfosuccinates;
· (C6-C30) alkyl sulfoacetates;
· (C6-C24) acylsarcosinates;
· (C6-C24) acylglutamates;
· (C6-C30) alkylpolyglycoside carboxylic ethers;
· (C6-C30) alkylpolyglycoside sulfosuccinates;
· (C6-C30) alkyl sulfosuccinamates;
· (C6-C24) acyl isethionates, for example sodium lauroyl methyl isethionate, sodium cocoyl isthionate; mentiones may be made of the sodium lauroyl methyl isethionate which is sold under the trade name
Figure PCTCN2016080201-appb-000004
LQ-CLR-SB by the company Innospec Active Chemicals;
· N- [ (C6-C24) acyl] taurates;
· salts of fatty acids;
· (C8-C20) acyl lactylates;
· salts of (C6-C30) alkyl-D-galactosiduronic acids;
· salts of (C6-C30) alkyl polyoxyalkylenated ether carboxylic acids, of (C6-C30) alkylaryl polyoxyalkylenated ether carboxylic acids or of (C6-C30) alkylamido polyoxyalkylenated ether carboxylic acids;
· and their mixtures.
The alkyl or acyl radicals of these various anionic surfactants preferably comprise from 12 to 20 carbon atoms.
Furthermore, the oxyalkylenated or polyoxyalkylenated anionic surfactants preferably comprise from 1 to 50 alkylene oxide groups, more preferably from 1 to 4 alkylene oxide groups, in particular ethylene oxide groups.
Advantageously, according to an embodiment, the present invention comprises at least one anionic surfactant chosen from (C6-C30) alkyl sulfates, (C6-C30) alkyl ether sulfates, (C6-C30) alkylamido ether sulfates, alkylaryl polyether sulfates, monoglyceride sulfates, (C6-C24) acyl isethionates, or a mixture thereof.
According to an embodiment of the present invention, the anionic surfactant is preferably chosen from sodium laureth sulfate, sodium lauroyl methyl isethionate, sodium cocoyl isethionate, or a mixture thereof.
More preferably the anionic surfactant is sodium laureth sulfate containing in average 2.2 ethylene oxide groups.
Advantageously, the content of anionic surfactant (s) represents from 1%to 70%by weight, preferably from 2%to 40%by weight, more preferably from 5%to 20%by weight, with respect to the weight of the composition.
ii) Amphoteric or zwitterionic surfactant (s)
The amphoteric or zwitterionic surfactant (s) that may be used in the present invention may be quaternized secondary or tertiary aliphatic amine derivatives containing at least one anionic group, for instance a carboxylate, sulfonate, sulfate, phosphate or phosphonate group, and in which the aliphatic group or at least one of the aliphatic groups is a linear or branched chain comprising from 8 to 22 carbon atoms.
Mention may be made in particular of (C8-C20) alkylbetaines, sulfobetaines, (C8-C20 alkyl) amido (C2-C8 alkyl) betaines and (C8–C20 alkyl) amido (C2-C8 alkyl) sulfobetaines.
Among the (C8-C20) alkylbetaines, mentions may be made of behenylbetaine, cetyl betaine, cocoylbetaine, decylbetaine. From alkylbetaines, cocoylbetaine is preferred, for example the products sold by the company Rhodia under the tradename
Figure PCTCN2016080201-appb-000005
BB/FLA.
Among the optionally quaternized secondary or tertiary aliphatic amine derivatives that  may be used, mention may also be made of the products of respective structures (A1) and (A2) below:
(A1)    Ra-CON (Z) CH2- (CH2m-N+ (Rb) (Rc) (CH2COO-)
in which:
Ra represents a C10-C30 alkyl or alkenyl group derived from an acid Ra-COOH preferably present in hydrolysed coconut oil, a heptyl group, a nonyl group or an undecyl group,
Rb represents a β-hydroxyethyl group,
Rc represents a carboxymethyl group;
m is equal to 0, 1 or 2,
Z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group;
(A2)    Ra’-CON (Z) CH2- (CH2m’-N (B) (B')
in which:
B represents -CH2CH2OX', with X'representing -CH2-COOH, CH2-COOZ’, -CH2CH2-COOH, -CH2CH2-COOZ’, or a hydrogen atom,
B'represents - (CH2z-Y', with z = 1 or 2, and Y'representing -COOH, -COOZ’, -CH2-CHOH-SO3H or -CH2-CHOH-SO3Z’,
m'is equal to 0, 1 or 2,
Z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group,
Z’represents an ion resulting from an alkali or alkaline-earth metal, such as sodium, potassium or magnesium; an ammonium ion; or an ion resulting from an organic amine and in particular from an amino alcohol, such as monoethanolamine, diethanolamine and triethanolamine, monoisopropanolamine, diisopropanolamine or triisopropanolamine, 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1, 3-propanediol and tris (hydroxymethyl) aminomethane,
Ra'represents a C10-C30 alkyl or alkenyl group of an acid Ra'COOH preferably present in hydrolysed linseed oil or coconut oil, an alkyl group, in particular a C17 alkyl group, and its iso form, or an unsaturated C17 group.
The compounds corresponding to formula (A1) are preferred.
Among the compounds corresponding to formula (A1) , mentions may be made of cocamidopropyl betaine, for example the product sold under the tradename Dehyton PK 45 by Cognis (BASF) .
Use may also be made of the compounds of formula (A3) :
(A3)    Ra”-NH-CH (Y”) - (CH2) n-C (O) -NH- (CH2) n’-N (Rd) (Re)
in which:
- Ra”represents a C10-C30 alkyl or alkenyl group of an acid Ra”-C (O) OH preferably present  in hydrolysed linseed oil or coconut oil;
- Y'’ represents the group –C (O) OH, -C (O) OZ” , -CH2-CH (OH) -SO3H or the group -CH2-CH (OH) -SO3-Z” , with Z” representing a cationic counterion resulting from an alkali metal or alkaline-earth metal, such as sodium, an ammonium ion or an ion resulting from an organic amine;
- Rd and Re represent, independently of each other, a C1-C4 alkyl or hydroxyalkyl radical; and
- n and n'denote, independently of each other, an integer ranging from 1 to 3.
Among the compounds corresponding to formula (A3) , mention may in particular be made of the compound classified in the CTFA dictionary under the name sodium diethylaminopropyl cocoaspartamide, such as the one sold by the company Chimex under the name Chimexane HB.
Preferably, the amphoteric surfactants are chosen from (C8-C20) alkylbetaines, (C8-C20) alkylamido (C1-C6) alkylbetaines, and mixtures thereof.
More preferably, the amphoteric or zwitterionic surfactant is chosen from cocamidopropyl betaine, cocoylbetaine, or a mixture thereof.
According to a preferred embodiment, the amphoteric or zwitterionic surfactant (s) is present in an amount ranging from 1%to 70%by weight, preferably from 3%to 50%by weight, more preferably from 5%to 15%by weight, relative to the total weight of the composition.
Nonionic surfactant (s)
According to the present invention, the composition comprises at least one nonionic surfactant selected from the group consisting of alkyl (poly) glycosides, fatty acid esters of glycerol and of polyglycerol, or a mixture thereof.
Preferably, according to an embodiment, the composition comprises a mixture of nonionic surfactants of alkyl (poly) glycoside and fatty acid esters of glycerol and of polyglycerol.
i) Alkyl (poly) glycoside nonionic surfactant (s)
The term “alkyl (poly) glycoside” denotes an alkylpolyglycoside or an alkylmonoglycoside, also referred to in the present patent application as an alkylglycoside, which may be alkoxylated with one or more alkylene oxide groups, preferentially of C2-C4.
The alkyl (poly) glycoside nonionic surfactant (s) used, alone or as mixtures, in accordance with the present invention may be represented by formula (IV) below:
R1O- (R2O) t- (G) v    (IV)
in which:
R1 represents a linear or branched, saturated or unsaturated alkyl group, containing from  about 8 to 24 carbon atoms, or an alkyl phenyl group in which the linear or branched alkyl radical contains from 8 to 24 carbon atoms,
R2 represents an alkylene group containing from about 2 to 4 carbon atoms,
G represents a saccharide unit containing 5 or 6 carbon atoms,
t denotes a value ranging from 0 to 10 and preferably from 0 to 4, and
v denotes a value ranging from 1 to 15.
Preferably, the alkyl (poly) glycoside nonionic surfactant (s) correspond to formula (IV) in which:
R1 denotes a linear or branched, saturated or unsaturated alkyl group containing from 8 to 18 carbon atoms,
G denotes glucose, fructose or galactose, preferably glucose,
t denotes a value ranging from 0 to 3, and is preferably equal to 0,
and R2 and v are as defined previously.
The degree of polymerization of the alkyl (poly) glycoside nonionic surfactant (s) as represented, for example, by the index v in formula (IV) ranges on average from 1 to 15 and preferably from 1 to 4. This degree of polymerization more particularly ranges from 1 to 2 and better still from 1.1 to 1.5, on average.
The glycoside bonds between the saccharide units are 1, 6-or 1, 4-bonds; preferably 1, 4-bonds.
The compounds of formula (IV) that may be used in the present invention are especially represented by the products sold by the company Cognis under the names
Figure PCTCN2016080201-appb-000006
 (600 CS/U, 1200 and 2000) or
Figure PCTCN2016080201-appb-000007
 (818, 1200 and 2000) . It is also possible to use the products sold by the company SEPPIC under the names Triton CG 110 (or Oramix CG 110) and Triton CG 312 (or
Figure PCTCN2016080201-appb-000008
NS 10) , the products sold by the company BASF under the name Lutensol GD 70, or those sold by the company Chem Y under the name AG10 LK.
It is also possible, for example, to use the 1, 4- (C8-C16) alkylpolyglucoside as an aqueous solution at 53%by weight relative to the total weight of the solution, sold by Cognis under the reference
Figure PCTCN2016080201-appb-000009
818 UP.
Among all these alkyl (poly) glycoside nonionic surfactants, the decyl glucoside (INCI: Decyl glucoside) sold by Cognis under the reference
Figure PCTCN2016080201-appb-000010
2000 UP is preferably used.
ii) Fatty acid ester (s) of glycerol and of polyglycerol
According to the invention, the composition may comprise at least one fatty acid ester of glycerol and/or of polyglycerol.
According to a preferred embodiment, the fatty acid ester (s) of polyglycerol is (are) chosen from esters resulting from the reaction of polyglycerol comprising from 2 to 12 glycerol units, preferably from 3 to 10 glycerol units, and of at least one fatty acid containing from 8 to 24 carbon atoms, preferably from 8 to 22 carbon atoms, better still from 10 to 20 carbon atoms and even better still from 10 to 18 carbon atoms. The fatty acids containing from 8 to 24 carbon atoms may be linear or branched, and saturated or unsaturated.
The fatty acids may be chosen from oleic acid, stearic acid, isostearic acid, lauric acid, palmitic acid, myristic acid, linoleic acid, capric acid and caprylic acid, or mixtures thereof.
The fatty acid esters of polyglycerol can be chosen from monoesters, diesters, triesters and tetraesters, polyesters and mixtures thereof. Use is preferably made of esters with a low degree of esterification, for instance fatty acid monoesters, diesters or triesters of polyglycerol, or a mixture. The fatty acid ester of polyglycerol can be in the form of a mixture of esters with a low degree of esterification, for instance a mixture of monoester and diester or a mixture of monoester, diester and triester.
According to one embodiment, the fatty acid ester of polyglycerol is chosen from esters resulting from the reaction of polyglycerol comprising from 3 to 10 glycerol units and of at least one fatty acid containing from 8 to 20 carbon atoms, preferably from 10 to 18 carbon atoms, such as oleic acid or linoleic acid.
Mention may in particular be made of polyglyceryl-2 distearate, in particular as sold by NIHON EMULSION under the name Emalex PGSA; polyglyceryl-10 decastearate, in particular as sold by TAIYO KAGAKU under the name Sunsoft Q-1810S; glyceryl oleate, in particular as sold by COGNIS under the name Monomuls 90-O 18; glyceryl stearate, in particular as sold by COGNIS under the name Cutina GMS V; polyglyceryl-5 hexastearate, in particular as sold by TAIYO KAGAKU under the name Sunsoft A-186E; polyglyceryl-10 pentaoleate, in particular as sold by TAIYO KAGAKU under the name Sunsoft Q-175S; polyglyceryl-10 pentastearate, in particular as sold by TAIYO KAGAKU under the name Sunsoft Q-185S; glyceryl caprylate/caprate, in particular as sold by STEPAN under the name Stepan Mild GCC; polyglyceryl-10 heptaoleate, in particular as sold by TAIYO KAGAKU under the name Sunsoft Q-177S; polyglyceryl-4 isostearate, in particular as sold by EVONIK GOLDSCHMIDT under the name Isolan GI 34; diisostearoyl polyglyceryl-3 dimer dilinoleate, in particular as sold by EVONIK GOLDSCHMIDT under the name Isolan PDI; glyceryl laurate, in particular as sold by COGNIS under the name Monomuls 90-L 12; polyglyceryl-5 trioleate, in particular as sold by TAIYO KAGAKU under the name Sunsoft A-173E; polyglyceryl-2 oleate, in particular as sold by TAIYO KAGAKU under the name Sunsoft Q-17B; polyglyceryl-5 trimyristate, in particular as  sold by TAIYO KAGAKU under the name Sunsoft A-143E; polyglyceryl-2 caprylate, in particular as sold by TAIYO KAGAKU under the name Sunsoft Q-81 B; polyglyceryl-2 laurate, in particular as sold by TAIYO KAGAKU under the name Sunsoft Q-12D.
According to one particular embodiment, the fatty acid which is suitable for the reaction with the ester (s) of polyglycerol comprises at least one hydroxyl group. This is the case for ricinoleic acid. Mention may in particular be made of polyglyceryl-3 ricinoleate (and) sorbitan isostearate, in particular as sold by CRODA under the name Arlacel 1690, polyglyceryl-3 ricinoleate, in particular as sold by AARHUSKARLSHAMN under the name Akoline PGPR.
According to another embodiment, the fatty acid which is suitable for the reaction with the ester (s) of polyglycerol is a polyacid comprising at least one hydroxyl group.
For the purpose of the present invention, the nonionic surfactant (s) is (are) present in the composition ranging from 0.05%to 20%by weight, preferably from 0.1%to 10%by weight, more preferably 0.5%to 5%by weight, relative to the total weight of the composition.
Protein extract of Moringa genus plant seeds
The composition according to the present invention comprises at least one protein extract of Moringa genus plant seeds.
The genus Moringa comprises some 14 species of plants (of which particularly Moringa peregrina, M. aptera, M concane six, M. drouhardii, M. hildebrandtit', M. longituba) , among which Moringa pterygosperma (synonym: Moringa oleifera) is the best known.
It is a tree that grows rapidly and which adapts very well to variable conditions, spread throughout the tropics, in Asia, Africa and South America. The fruits are 30 to 50 cm long, hanging like drumsticks, from which comes the English name "drumstick tree" , and its green pods are used as vegetables throughout the world.
The seeds of Moringa are characterized by the presence of an oil whose content varies between 21 and 53%according to the species and maturity of the seeds.
In addition to their oil content, Moringa seeds are found to comprise compounds of proteic nature (see particularly the article “Isolation and characterization of a flocculating protein from Moringa oleifera lam” by U. Gassenschmidt, K.D. Jany, B. Tausche and H.R. Niebergall, Biochimica and biophysics acta, 1243: 477-481, 1995- “Active agents and mechanism of coagulation of turbid waters using Moringa oleifera” , of A. Ndabigengesere, K. Subba Narasiah and B.G. Talbot, Water research, 29, 2: 703-710, 1995) .
According to a preferred embodiment, the composition of the present invention comprises at least one protein extract of the seeds of Moringa oleifera.
The extract is preferably obtained from delipidated flour of Moringa oleifera seeds, and  was then extracted in a buffered aqueous medium, and then isolated by cation exchange chromatography.
Preferably, the protein extract is obtained in an aqueous medium with a pH of greater than or equal to 3, preferably from 3 to 8.
The protein extract according to the present invention is also disclosed, for example, in the patent application US 6,500,470 B1.
Mentions maybe made of commercially available products, such as those sold under the name Purisoft POE LS 9726 by the company BASF.
Preferably, for the purpose of the present invention, the protein extract of Moringa genus plant seeds is present in the composition in an amount ranging from 0.001%to 5%by weight, preferably from 0.001%to 2%by weight, relative to the total weight of the composition.
Cationic Polymer (s)
The composition of the present invention comprises at least one cationic polymer selected from cationic cellulose.
It is first recalled that, for the purposes of the present invention, the term “cationic polymer” denotes any polymer containing cationic groups and/or groups that can be ionized into cationic groups.
The cationic polymers that may be used preferably have a weight-average molar mass (Mw) of between 500 and 5×106 approximately and preferably between 103 and 3×106 approximately.
The cationic celluloses may be made more particularly chosen from cellulose ether derivatives comprising quaternary ammonium groups, cationic cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer, or a mixture thereof.
The cellulose ether derivatives comprising quaternary ammonium groups are especially described in French patent 1 492 597, and mention may be made of the polymers (INCI name polyquaternium-10) sold under the name Ucare Polymer “JR” (JR 400 LT, JR 125 and JR 30M) or “LR” (LR 400 or LR 30M) by the company Amerchol. These polymers are also defined in the CTFA dictionary as quaternary ammoniums of hydroxyethylcellulose that have reacted with an epoxide substituted with a trimethylammonium group.
Cationic cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer are described especially in US patent 4 131 576, and mention may be made of hydroxyalkylcelluloses, for instance hydroxymethyl-, hydroxyethyl-or hydroxypropylcelluloses grafted, in particular, with a methacryloylethyltrimethylammonium, methacrylamidopropyltrimethylammonium or dimethyldiallylammonium salt. The commercial  products corresponding to this definition are more particularly the products sold under the names Celquat L 200 and Celquat H 100 by the company National Starch.
Preferably, the cationic cellulose of the present invention is chosen from cellulose ether derivatives, more particularly comprising quaternary ammonium groups.
According to a preferred embodiment, the cationic polymer is present in the composition of the present invention, ranging from 0.01%to 3%by weight, preferably from 0.05%to 2%by weight, more preferably 0.1%to 1.5%by weight, relative to the total weight of the composition.
Oil (s)
The composition of the present invention comprises at least one hydrocarbon-based oil.
The term "oil" means any nonionic lipophilic compound that is insoluble in water and liquid at room temperature (25℃) and at atmospheric pressure.
For the purposes of the present invention, the term "water-insoluble" refers to a compound whose solubility at spontaneous pH in water at 25℃ and at atmospheric pressure is less than 1%and preferably less than 0.5%. The oils preferably have a melting point of less than 5℃ and a viscosity of less than 500 cPs at 25℃ at a shear rate of 1 s-1.
The term “hydrocarbon-based oil” is understood to mean oil essentially formed and even composed, of carbon and hydrogen atoms and optionally of oxygen and nitrogen atoms which does not comprise a silicone or fluorine atom; it can comprise ester, ether, amine and amide groups.
The oil may be volatile or non-volatile.
The term "non-volatile" means an oil of which the vapor pressure at 25℃ and atmospheric pressure is non-zero and is less than 0.02 mmHg (2.66 Pa) and better still less than 10-3 mmHg (0.13 Pa) .
The term “volatile oil” means an oil of which the vapor pressure at 25℃ and atmospheric pressure is from 0, 13 Pa to 40.000 Pa (0, 001 to 300 mmHg) and preferably from 1, 3 to 1300 Pa (0, 01 to 10 mm Hg) .
According to a preferred embodiment, the composition of the present invention comprises at least one oil selected from the group consisting of plant oil, hydrocarbon oil, or a mixture thereof.
In particular, the term "plant oil" means an oil as defined above, obtained from a species belonging to the plant kingdom.
Hydrocarbon oils are also referred to as mineral oils. The term “hydrocarbon oils” or "mineral oils" refers to complex substances of hydrocarbons in the form of linear, branched, or cyclic, saturated or unsaturated oils. These oils are obtained from crude petroleum oils by  distillation and refining. Hydrocarbon oils, or mineral oils are a complex of alkanes, cycloalkanes, aromatic hydrocarbons, or mixtures thereof. More preferably the hydrocarbon oils contain a chain with 15-40 carbon atoms.
As examples of hydrocarbon oils or mineral oils that may be used in the present invention, mention may be made of:
- mixtures of hydrocarbon-based oils derived from petroleum (INCI name: Mineral Oil) ,
- volatile or non-volatile liquid paraffin,
- liquid petroleum jelly,
- polyolefins and in particular polydecenes,
- isoparaffins such as isohexadecane, isododecane and hydrogenated polyisobutylenes such as
Figure PCTCN2016080201-appb-000011
oil sold by the company NOF Corporation (INCI name: Hydrogenated polyisobutene) .
Among the mineral oils mentioned above, the following are preferably used:
- mixtures of hydrocarbon-based oils derived from petroleum,
- volatile or non-volatile liquid paraffin, and
- liquid petroleum jelly, and
- polyolefins and in particular polydecenes.
The term "polydecenes" means any compound of formula C10nH (20n) +2 in which n ranges from 3 to 9, corresponding to the name “polydecene” in the CTFA dictionary, 7th edition, 1997 of the Cosmetic, Toiletry and Fragrance Association, USA, and also to the same INCI name in the USA and in Europe. These are poly-1-decene hydrogenation products. Among these compounds, those for which, in the formula, n ranges from 3 to 7 are more particularly chosen according to the invention.
Examples that may be mentioned include the products sold under the name
Figure PCTCN2016080201-appb-000012
366 NF Polydecene by the company Amoco Chemical, and those sold under the names
Figure PCTCN2016080201-appb-000013
2002 FG, 2004 FG, 2006 FG and 2008 FG by the company Fortum.
The preferred hydrocarbon oil is mixtures of hydrocarbon-based oils derived from petroleum (INCI name: Mineral Oil) , volatile or non-volatile liquid paraffin, or a mixture thereof.
Mentions may be made of the product (INCI name: mineral oil) sold under the tradename Emcaplus 70 by the company Oxiteno.
As examples of plant oils that are suitable for the present invention, mentions maybe made of:
- sweet almond oil,
- argan oil,
- avocado oil,
- peanut oil,
- camellia oil,
- safflower oil,
- calophyllum oil,
- coconut oil,
- colza oil,
- copra oil,
- coriander oil,
- cucurbit oil,
- wheatgerm oil,
- jojoba oil or jojoba liquid wax,
- linseed oil,
- macadamia oil,
- maize germ oil,
- hazelnut oil,
- walnut oil,
- vernonia oil,
- apricot kernel oil,
- olive oil,
- evening primrose oil,
- palm oil,
- passionflower oil,
- grapeseed oil,
- rose oil,
- castor oil,
- rye oil,
- sesame oil,
- rice bran oil,
- soya oil, or soybean oil, and
- sunflower oil.
Preferably, the composition of the present invention comprises at least one hydrocarbon oil.
The total amount of oil (s) , when they are present in the composition, preferably ranges  from 0.01%to 20%by weight, better still from 0.05%to 10%by weight and more particularly from 0.1%to 5%by weight relative to the total weight of the final composition.
According to a preferred embodiment, the present invention relates to a composition for treating keratin fibers, comprising, by weight relative to the total weight of the composition:
a) from 5%to 20%by weight of at least one surfactant selected from the group consisting of anionic surfactants, amphoteric or zwitterionic surfactants, or a mixture thereof;
b) from 0.1%to 10%by weight of at least one nonionic surfactant selected from alkyl (poly) glycosides, fatty acid esters of glycerol and of polyglycerol, or a mixture thereof;
c) from 0.001%to 2%by weight of at least one protein extract of moringa genus plant seed;
d) from 0.05%to 2%by weight of at least one cationic polymer chosen from quaternary ammoniums of hydroxyethylcellulose that have reacted with an epoxide substituted with a trimethylammonium group; and
e) from 0.05%to 10%by weight of at least one hydrocarbon-based oil selected from plant oil, hydrocarbon oil, or a mixture thereof.
Galenic form
The composition according to the invention may take the form of thickened liquid, creams or gel. It is preferable that the composition according to the present invention be in the form of an nano-or micro-emulsion, more particularly oil-in-water nano-or micro-emulsion.
These emulsions can be prepared in particular by the phase inversion temperature technique (PIT emulsions) , in which the average size of the globules constituting the oily phase is within given limits, namely between 0.1 and 4 μm (100 to 4000 nm) . The principle of phase inversion temperature (or PIT) emulsification is, in theoretical terms, well known to those skilled in the art; it was described in 1968 by K. Shinoda (J. Chem. Soc. Jpn., 1968, 89, 435) . It was shown that this emulsification technique makes it possible to obtain stable fine emulsions (K. Shinoda and H. Saito, J. 
Figure PCTCN2016080201-appb-000014
Interface Sci., 1969, 30, 258) . This technology was applied in cosmetics as early as 1972 by Mitsui et al. ( “Application of the phase-inversion-temperature method to the emulsification of cosmetics” ; T. Mitsui, Y. Machida and F. Harusawa, American. Cosmet. Perfum, 1972, 87, 33) .
The compositions according to the invention may naturally contain, in addition, all the standard adjuvants encountered in the field of shampoos, such as, for example, perfumes, preservatives, sequestering agents, thickeners, hydrating agents, anti-dandruff or antiseborrhoeic agents, vitamins, sunscreen agents, suspending agents and the like.
Method and use
The present invention also relates to a process for washing keratin fibers, especially the hair, comprising the steps of applying to said fibers the composition of the invention, and then washing with water after an optional period of exposure. The process as mentioned above is preferably a process for washing and conditioning keratin fibers, in particular the hair.
Another aspect of the present invention is the use of the above composition of the invention for washing and conditioning keratin fibers, especially hair.
Preferably, the present invention further relates to the use of the above composition in reducing the deposition of fine particles contained in the air on keratin fibers, in particular the hair.
Non limiting examples illustrating the invention are given.
EXAMPLES
Three hair shampoos were prepared, one according to the invention (Invention formulas A, B) and three comparative (Comparative formula A’, B’and B” ) :
Figure PCTCN2016080201-appb-000015
Figure PCTCN2016080201-appb-000016
Figure PCTCN2016080201-appb-000017
Comparative formula A’corresponds to the invention formula A and contains a polymer other than the one claimed in the present invention; Comparative formula B’corresponds to the invention formula B and contains silicone oil instead of the oil as claimed in the present invention; Comparative formula B” also corresponds to the invention formula B and contains a nonionic surfactant other than the one claimed in the present invention.
The invention and comparative formulas were prepared according to the conventional methods for preparing shampoo formulations. The ingredients listed above were mixed until homogeneous at room temperature (20-25℃) .
The invention and comparative formulas were subject to the evaluations, including the conditioning effect, anti-particle deposition effect, and transparency.
The transparency was evaluated by the turbidity, using a 2100N Turbidimeter machine from HACH.
The term “transparent” is understood to mean a composition having a turbidity of less than 250 NTU (Nephelometric Turbidity Units) at 25℃ and preferably of less than 150 NTU at 25℃, even more preferably less than 100 NTU at 25℃.
The conditioning effect was evaluated by a hair dresser by using each of the invention or comparative formulas on 6 women consumers as hair shampoos, then combing the hair for 10 minutes. Finally the scores were given to the formulas, respectively:
1: very poor conditioning effect, hair is totally tangled and very dry after application, very difficult to comb;
2: poor conditioning effect, hair is tangled or dry after application, not easy to comb;
3: good conditioning effect, hair is smooth, soft, and detangled, easy to comb;
4: very good conditioning effect, hair is very smooth and supple, very easy to comb.
The formula was considered to have an expected conditioning when the average score of the formula is greater than or equal to 2.5.
Lastly, the anti-particle deposition effect of the invention and comparative formulas was evaluated following the protocol of:
1. apply the invention formula A, B, comparative formula A’, B’and B” , respectively, on dry hair swatch as rinse off shampoo product;
2. apply carbon powders to the hair swatch prepared from the previous step using a fan blowing the carbon powders to the swatch;
3. take photo of the hair swatch using SEM image analyzing equipment SEM sold by the company JOEL under the name JSM-606OLA, and analyze the carbon powder deposition on the hair swatch using image analyzing process.
The carbon powders used in the evaluation were intended to simulate the fine particles or in particular PM 2.5 contained in the air. The particle size of the carbon powder in aqueous solution, when tested with Malvern Mastersizer 3000, distributed from 0.5 μm to 10 μm, which corresponds to the particle size of the fine particles in the air, including PM 2.5.
The composition of the PM 2.5, or fine particles is dependent on location and season. As an example in China, PM 2.5 comprises, but not limited to: geological materials such as paved or unpaved roads, constructions, agricultural operations, wind-blown soil; organic matters from cooking, residential heating, field burning of crop residue, forest fires, and grassland fires; organic carbon such as conversion of volatile organic compounds; ammonium, sulfates, nitrates, and fugitive dust, see in “Winter and Summer PM 2.5 Chemical Compositions in Fourteen Chinese Cities” Jun-ji CAO, etc., Journal of the Air and Waste Management Association, 24th, Sep, 2012.
More specifically, the swatch treated with invention formula and comparative formulas were placed in a chamber equipped with carbon powders, one fan, and one particle detector, by fixing one end of the hair swatch on a horizontally positioned shelf.
The fan was placed in the center of the chamber. A watch glass with 0.1 g carbon black powder was placed under the fan, right in the center. A particle detector (Dust Trak II Model 8532 sold by the company TSI) was placed in the chamber and finally the chamber of the device was closed.
The fan was then turned on for 10 minutes, and then turned off. After 5 minutes, the swatches were moved out from the chamber and observed under SEM.
The anti-particle deposition effect of the formulas was represented by particle deposition coverage value, obtained by image analyzing tools which are conventionally available.
The lower the value of particle deposition coverage, the better the anti-particle deposition effect is.
The results of the evaluation were listed herewith.
Figure PCTCN2016080201-appb-000018
As shown in the table listed above, comparing to the corresponding comparative formulas, invention formula A and B both have good conditioning effect on the hair, and both have improved anti-particle deposition effect, meanwhile are transparent. Whereas even though the conditioning effect is good, neither of the comparative formula B’or B” has a transparent esthetic appearance, and moreover, the anti-particle deposition effect is poor comparing to the invention formula B. Comparative formula A’possesses a transparent appearance, however it does not have a good balance of conditioning effect and anti-particle deposition effect, comparing to the invention formula A, i.e., both of which are worse than that of the invention formula A.

Claims (16)

  1. A transparent composition for treating keratin fibers, comprising:
    a) at least one surfactant selected from the group consisting of anionic surfactants, amphoteric or zwitterionic surfactants, or a mixture thereof;
    b) at least one nonionic surfactant selected from alkyl (poly) glycosides, fatty acid esters of glycerol and of polyglycerol, or a mixture thereof;
    c) at least one protein extract of moringa genus plant seed;
    d) at least one cationic polymer chosen from cationic cellulose; and
    e) at least one hydrocarbon-based oil.
  2. Composition of claim 1 is silicone-free, preferably the composition does not contain silicone.
  3. Composition of claim 1 or 2, wherein the anionic surfactant is chosen from (C6-C30) alkyl sulfates, (C6-C30) alkyl ether sulfates, (C6-C30) alkylamido ether sulfates, alkylaryl polyether sulfates or monoglyceride sulfates, or a mixture thereof; preferably chosen from sodium laureth sulfate, sodium lauroyl methyl isethionate, sodium cocoyl isethionate, or a mixture thereof; more preferably chosen from sodium laureth sulfate containing 1 to 4 ethylene oxide groups.
  4. Composition of any one of the preceding claims 1 to 3, wherein the amphoteric or zwitterionic surfactant is chosen from (C8-C20) alkylbetaines, (C8-C20 alkyl) amido (C2-C8 alkyl) betaines, or a mixture thereof; more preferably chosen from cocoylamidopropylbetaine, cocoylbetaine, or a mixture thereof.
  5. Composition of any one of the preceding claims 1 to 4, wherein the surfactant a) is present in an amount ranging from 1% to 70% by weight, preferably from 3% to 50% by weight, more preferably from 5% to 20% by weight, relative to the total weight of the composition.
  6. Composition of any one of the preceding claims 1 to 5, wherein the alkyl (poly) glycoside nonionic surfactant is chosen from, alone or as a mixture, compounds of formula (IV) ,
    R1O- (R2O) t- (G) v (IV)
    in which:
    R1 represents a linear or branched, saturated or unsaturated alkyl group, containing from 8 to 24 carbon atoms, or an alkyl phenyl group in which the linear or branched alkyl radical contains 8 to 24 carbon atoms, preferably R1 represents a linear or branched, saturated or unsaturated alkyl group containing from 8 to 18 carbon atoms,
    R2 represents an alkylene group containing from 2 to 4 carbon atoms,
    G represents a saccharide unit containing 5 or 6 carbon atoms, preferably glucose, fructose or galactose, more preferably glucose, t denotes a value ranging from 0 to 10 and preferably from 0 to 4, and
    v denotes a value ranging from 1 to 15, preferably 1 to 4.
  7. Composition of any one of the preceding claims 1 to 6, wherein the fatty acid ester of glycerol and of polyglucerol is selected from the group consisting of esters resulting from the reaction of polyglycerol comprising from 3 to 10 glycerol units and of at least one fatty acid containing from 8 to 20 carbon atoms, preferably from 10 to 18 carbon atoms; preferably selected from glyceryl oleate.
  8. Composition of any one of the preceding claims 1 to 7, wherein the nonionic surfactant is present in an amount ranging 0.05% to 20% by weight, preferably from 0.1% to 10% by weight, more preferably 0.5% to 5% by weight, relative to the total weight of the composition.
  9. Composition of any one of the preceding claims 1 to 8, wherein the protein extract of Moringa genus plant seeds is a protein extract of the seeds of Moringa oleifera.
  10. Composition of any one of the preceding claims 1 to 9, wherein the protein extract of Moringa genus plant seeds is present in the composition in an amount ranging from 0.001% to 5% by weight, preferably from 0.001% to 2% by weight, relative to the total weight of the composition.
  11. Composition of any one of the preceding claims 1 to 10, wherein the cationic polymer is chosen from cellulose ether derivatives comprising quaternary ammonium groups; preferably chosen from quaternary ammoniums of hydroxyethylcellulose that have reacted with an epoxide substituted with a trimethylammonium group.
  12. Composition of any one of the preceding claims 1 to 11, wherein the cationic polymer is present in an amount ranging from 0.01% to 3% by weight, preferably from 0.05% to 2% by weight, more preferably 0.1% to 1.5% by weight, relative to the total weight of the composition.
  13. Composition of any one of the preceding claims 1 to 12, wherein the hydrocarbon-based oil is selected from the group consisting of plant oil, hydrocarbon oil, or a mixture thereof; preferably selected from soybean oil, coconut oil, volatile or non-volatile liquid paraffin, petroleum, or a mixture thereof.
  14. Composition of any one of the preceding claims 1 to 13, wherein the hydrocarbon-based oil is present in an amount ranging from 0.01% to 20% by weight, better still from 0.05% to 10% by weight and more particularly from 0.1% to 5% by weight, relative to the total weight of the composition.
  15. Method for washing keratin fibers, especially the hair, comprising the steps of applying to said fibers the composition according to any one of the preceding claims 1 to 14, and then washing with water after an optional period of exposure.
  16. Use of the composition of any one of the preceding claims 1 to 15 in reducing particle deposition on keratin fibers, in particular hair.
PCT/CN2016/080201 2016-04-26 2016-04-26 Composition for treating keratin fibers WO2017185227A1 (en)

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WO2006029757A1 (en) * 2004-09-16 2006-03-23 Hans Schwarzkopf & Henkel Gmbh & Co. Kg Active agent mixtures for the treatment of keratin fibres
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US20040096417A1 (en) * 2002-11-14 2004-05-20 Robert Kleiman Moringa esters and cosmetic and pharmaceutical preparations and methods of manufacture thereof
WO2006029757A1 (en) * 2004-09-16 2006-03-23 Hans Schwarzkopf & Henkel Gmbh & Co. Kg Active agent mixtures for the treatment of keratin fibres
EP1810660A1 (en) * 2006-01-18 2007-07-25 Henkel Kommanditgesellschaft auf Aktien Hair treatment composition comprising plant extracts and UV-filter
CN101940541A (en) * 2008-10-15 2011-01-12 莱雅公司 Fatty acid-free, foaming cosmetic composition and method of use
CN101485622A (en) * 2009-03-03 2009-07-22 张嘉恒 Shampoo containing extract of Moringa oleifera and preparation method thereof
CN102458355A (en) * 2009-06-22 2012-05-16 皮尔法伯护肤化妆品公司 Extract of whole seeds of moringa sp., and use thereof in cosmetic and/or dermatological compositions

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