US20150050230A1 - Compositions and Methods for Treating Damaged Hair - Google Patents

Compositions and Methods for Treating Damaged Hair Download PDF

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US20150050230A1
US20150050230A1 US14/354,827 US201414354827A US2015050230A1 US 20150050230 A1 US20150050230 A1 US 20150050230A1 US 201414354827 A US201414354827 A US 201414354827A US 2015050230 A1 US2015050230 A1 US 2015050230A1
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hair
composition
alkyl
compositions
dimethicone
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Sen Yang
Allwyn Colaco
Michael J. Fair
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Avon Products Inc
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Avon Products Inc
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Priority to US14/354,827 priority Critical patent/US20150050230A1/en
Assigned to AVON PRODUCTS, INC. reassignment AVON PRODUCTS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: YANG, SEN, FAIR, MICHAEL J., COLACO, ALLWYN
Publication of US20150050230A1 publication Critical patent/US20150050230A1/en
Assigned to CITIBANK, N.A. reassignment CITIBANK, N.A. SECURITY INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: AVON PRODUCTS, INC.
Assigned to AVON PRODUCTS, INC. reassignment AVON PRODUCTS, INC. RELEASE OF SECURITY INTEREST IN PATENTS Assignors: CITIBANK, N.A.
Priority to US15/801,832 priority patent/US10874598B2/en
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/002—Preparations for repairing the hair, e.g. hair cure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/12—Preparations containing hair conditioners
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects

Definitions

  • the present invention relates to methods and compositions for strengthening keratin fibers and for repairing damaged keratin fibers.
  • the present invention relates to hair care compositions, such as shampoos and conditioners, that comprise effective amounts of 3,3′-thiodipropionic acid (TDPA) or a derivative thereof which strengthen and repair damaged hair of the scalp.
  • TDPA 3,3′-thiodipropionic acid
  • a number of products and treatments are available to consumers to modify the appearance of human hair, including hair dyes, lighteners or bleaches, permanent treatments, and the like. Some of these treatments employ harsh chemicals or heat which may damage and weaken human hair. Even less harsh treatments, including blow drying or even brushing or combing or hair can cause damage over time. Exposure to excessive UV radiation from the sun and environmental insults, including chemicals in swimming pools, may likewise damage hair. The cumulative result of these factors is often dry, brittle hair that is prone to breaking or splitting.
  • compositions which strengthen hair to prevent or remediate the effects of chemical, mechanical, and environmental damage. It is therefore an object of the invention to provide compositions, including shampoos and hair conditioners, which strengthen and repair damaged hair of the scalp. It is a further object of the invention to provide treatment regimens for preventing or remediating damage to the hair, particularly hair that has been artificially colored or lightened.
  • compositions for preventing, reversing, remediating, and/or forstalling damage to human hair of the scalp, and in particular, hair which has been previously artificially colored or lightened.
  • compositions are provided comprising, in a topically acceptable vehicle, effective amounts of compounds having the structure shown of Formula (I).
  • X is selected from —O—, —S—, —CH 2 —, —NH—, or —NR N — (where R N is methyl or ethyl), but will typically be —S—, and R 1 and R 2 are independently selected from hydrogen, C 1-22 hydrocarbon radicals, and cations (e.g., ammonium, quaternary amines, alkali or alkali-earth metals, etc.).
  • X is —S—
  • R 1 and R 2 are hydrogen
  • the compound of Formula (I) is 3,3′-thiodipropionic acid (TDPA).
  • R 1 and/or R 2 are independently selected from C 1-20 hydrocarbon radicals.
  • R 1 and/or R 2 are independently selected from C 1-15 hydrocarbon radicals. In some embodiments, R 1 and/or R 2 are independently selected from C 1-10 hydrocarbon radicals. In some embodiments, R 1 and/or R 2 are independently selected from C 1-5 hydrocarbon radicals.
  • a hair care product comprising an effective amount of a compound of Formula (I) (e.g., TDPA) in a topically acceptable vehicle, such as an aqueous solution or emulsion.
  • a topically acceptable vehicle such as an aqueous solution or emulsion.
  • the hair care product will be a hair conditioner that is either of the rinse-off or leave-in variety.
  • methods of treating the hair comprising applying a composition comprising and effective amount of a compound of Formula (I) (e.g., TDPA), to the hair at least once weekly, more typically at least once daily, for a period sufficient to show improvement in the strength of the hair (e.g., tensile strength, resistance to breaking, and/or fewer split ends, etc.) or the overall aesthetic appearance of the hair.
  • the duration of treatment will typically be at least five days, more typically at least one or two weeks, or longer.
  • FIG. 1 illustrates the tensile load required to break hair fibers that were untreated, treated with vehicle, or treated with vehicle plus TDPA.
  • alkyl is intended to embrace straight-chained, branched, or cyclic hydrocarbons, particularly those having from one to 20 carbon atoms, and more particularly C 1-12 hydrocarbons.
  • Keratin fiber includes hair of the scalp, eyelashes, eyebrows, facial hair, and body hair such as hair of the arms, legs, etc. Keratin fibers are not limited to humans and also include any keratin fibers from a mammal, such as, for example, pet hair and mammalian fur.
  • the compounds of the invention will generally have the structure shown of Formula (I).
  • X is selected from —O—, —S—, —CH 2 —, —NH—, or —NR N — (where R N is methyl or ethyl), but will typically be —S—.
  • R 1 and R 2 are independently selected from hydrogen, C 1-22 hydrocarbon radicals, and cations (e.g., ammonium, quaternary amines, alkali or alkali-earth metals, etc.). In some embodiments R 1 and/or R 2 are hydrogen. In the case where R 1 and R 2 are hydrogen, the compound of Formula (I) is 3,3′-thiodipropionic acid (TDPA). Salts of TDPA are also contemplated including the case where one or both of the carboxylic acids are ionized. Cosmetically acceptable counterions (i.e., cations) usually, but not necessarily, are formed by the acid addition reaction with pH adjusters such as sodium hydroxide, triethanolamine, and the like.
  • pH adjusters such as sodium hydroxide, triethanolamine, and the like.
  • R 1 and/or R 2 are C 1-22 hydrocarbon radicals, including, without limitation, alkyl, alkenyl (e.g., vinyl, allyl, etc.), alkynyl, aryl (e.g., phenyl), alkyl-aryl (e.g., benzyl), aryl-alkyl (e.g., methylphenyl), heteroaryl, and combinations thereof.
  • the C 1-22 hydrocarbon radicals may be substituted with 1-10 heteroatoms, such as halogen, oxygen, nitrogen, and sulfur.
  • R 1 and R 2 may include halo (perfluoro, etc.), hydroxyl, alkoxy, epoxy, carboxy, oxa, oxo, ether, ester, amino, or amide groups, to name a few, including, without limitation, groups of the form —(RO) n — where R is ethyl or propyl and n is an integer from 1 to 10, and the like.
  • R 1 and/or R 2 is an alkyl or alkenyl group (linear, branched, or straight chained) having from 1-22 carbon atoms, or from 2-18 carbon atoms, including, without limitation, C 8 (e.g., capryl), C 10 (e.g., capric), C 12 (e.g., lauryl), C 14 (e.g., myristyl), C 16 (e.g., cetyl), C 18 (e.g., stearyl), C 20 (e.g., arachidyl), and C 22 (e.g., behenyl) alkyl or alkenyl groups.
  • R 1 and/or R 2 are lauryl groups.
  • the compounds may be mono-esters or TDPA (or a salt) or di-ester of TDPA.
  • 3,3′-thiodipropionic acid is the compound of Formula (I) where X is —S— and R 1 and R 2 are each hydrogen.
  • the other compounds of Formula (I) are referred to herein as “derivatives” of 3,3′-thiodipropionic acid (TDPA). Only those derivatives that are safe for contact with human integuments are considered appropriate for use in accordance with the invention.
  • compositions will usually comprise a compound of Formula (I) (such as TDPA) in an amount from about 0.1% to about 5% by weight of the total composition. More typically, the compositions will comprise a compound of Formula (I) (e.g., TDPA) in an amount from about 0.25% to about 2.5% by weight or from about 0.5 to about 1.5% by weight of the total composition. In one embodiment, the compositions will comprise a compound of Formula (I) (e.g., TDPA) in an amount form about 0.75% to about 1.25% or about 1% by weight of the total composition.
  • TDPA compound of Formula (I)
  • compositions may further comprise additional agents that impart strength to the hair, including, without limitation amino acids, creatine, cysteine, and ceramides, to name a few.
  • the compositions may be free of additional hair strengthening ingredients.
  • the compositions will further comprise creatine, for example, in an amount from about 0.01 to about 5% by weight.
  • the compositions will be essentially free of creatine, by which is meant that the amount of creatine is insufficient to impart a measurable improvement in hair strengthening.
  • the compositions will be free of creatine.
  • compositions will typically comprise a topically acceptable vehicle.
  • topically acceptable is meant that the vehicle is safe for contact with a human integument.
  • the vehicle may comprise a liquid, comprising a single phase, a dual-phase system, or an emulsion.
  • the compositions can be aqueous or anhydrous, but will typically be in the form of an aqueous solution, dispersion, or emulsion, such as a water-in-oil, oil-in-water, silicone-in-water, water-in-silicone, or multiple emulsion, or the like.
  • an emulsifier or a stabilizer is typically included.
  • the vehicle comprises a volatile solvent.
  • a volatile solvent may have a vapor pressure of above about 0.01 mmHg at 20° C.
  • Volatile solvents may include water, volatile C 5-12 hydrocarbons (e.g., isododecane), volatile silicones (e.g., cyclopentasiloxane), lower alcohols (e.g., ethanol, isopropyl alcohol, etc.), and the like.
  • the volatile solvents may comprise up to about 99% (w/w) of the composition, more typically up to about 85% (w/w) of the composition.
  • compositions may comprise and oil or an oil-containing phase may be composed of a singular oil or mixtures of different oils.
  • oils include vegetable oils; esters such as octyl palmitate, isopropyl myristate and isopropyl palmitate; ethers such as dicapryl ether; fatty alcohols such as cetyl alcohol, stearyl alcohol and behenyl alcohol; isoparaffins such as isooctane, isododecane and isohexadecane; silicone oils such as dimethicones, cyclic silicones, and polysiloxanes; hydrocarbon oils such as mineral oil, petrolatum, isoeicosane and polyisobutene; natural or synthetic waxes; and the like.
  • Non-volatile silicone oils will include polydimethylsiloxanes and other polyalkylsiloxanes, polyarylsiloxanes, polyalkylarylsiloxanes, or mixtures thereof.
  • the non-volatile silicone oils will typically have a viscosity from about 10 to about 60,000 centistokes at 25° C. and a boiling point greater than 250° C. at atmospheric pressure.
  • Non limiting examples include dimethyl polysiloxane (dimethicone), phenyl trimethicone, and diphenyldimethicone.
  • volatile and non-volatile silicone oils may optionally be substituted with various functional groups such as alkyl, aryl, amine groups, vinyl, hydroxyl, haloalkyl groups, alkylaryl groups, and acrylate groups, to name a few.
  • compositions may include natural or synthetic film-forming polymers, including, without limitation, those that assist in styling and setting hair.
  • natural polymers include shellac, alginates, gelatines, pectines, chitosan salts, and cellulose derivatives.
  • Synthetic polymers that can be used are, for example, polyvinylpyrrolidone, polyvinyl acetate, polyacryl compounds such as acrylic acid or methacrylic acid polymers, basic polymers of esters of these two acids with aminoalcohols or the salts or quarternization products of these basic polymers, polyacrylnitrile, and copolymers of such compounds, for example, polyvinylpyrrolidone vinyl acetate or polyvinylpyrrolidone dimethylaminoethylmethacrylate.
  • polymeric film formers include polyolefins, polyvinyls, polacrylates, polyurethanes, silicone elastomers, silicone resins, silicone-polyalkylene oxide copolymers, silicone acrylates, polyamides, polyesters, fluoropolymers, polyethers (e.g., PEG, PPG, and copolymers), polyacetates, polycarbonates, polyimides, rubbers (e.g., di- and tri-block copolymer elastomers or styrene, ethylene, propylene, and/or butylene), epoxies, formaldehyde resins, and homopolymers and copolymers of and of the foregoing.
  • polyethers e.g., PEG, PPG, and copolymers
  • polyacetates e.g., polycarbonates, polyimides, rubbers (e.g., di- and tri-block copolymer elastomers or st
  • Suitable polymeric film formers include silicone polymers, acrylates, alkyl acrylates, polyurethanes, fluoropolymers such as Fluomer (polyperfluoroperhydrophenanthrene) and silicone acrylates such as acrylates/dimethicone copolymers sold under the trade names KP-545 or KP 550 (Shin-Etsu).
  • Suitable film formers include, but are not limited to, Amino Bispropyl Dimethicone, Aminopropyl Dimethicone, Amodimethicone, Amodimethicone Hydroxystearate, Behenoxy Dimethicone, C 30-45 Alkyl Dimethicone, C 24-28 Alkyl Dimethicone, C 30-45 Alkyl Methicone, Cetearyl Methicone, Cetyl Dimethicone, Dimethicone, Dimethoxysilyl Ethylenediaminopropyl Dimethicone, Hexyl Methicone, Hydroxypropyldimethicone, Stearamidopropyl Dimethicone, Stearoxy Dimethicone, Stearyl Methicone, Stearyl Dimethicone and Vinyl Dimethicone.
  • silicone polymers including Methicone (as described by CTFA Monograph No. 1581, which is incorporated herein by reference), Dimethicones (as described by CTFA Monograph No. 840, which is incorporated herein by reference) and Amodimethicones as described by CTFA Monograph No. 189, which is incorporated herein by reference).
  • the film forming polymer is a silicone acrylate, such as that having the CTFA Monograph No. 10082 and the INCI name Acylates/Dimethicone. This polymer is commercially available from ShinEtsu Chemical Co., Ltd. under the trade name KP-544.
  • the film forming polymer may be a silicone urethane, such as that having the INCI Name Bis-Hydroxypropyl Dimethicone/SMDI Copolymer and the INCI Monograph ID No. 22006. This polymer is commercially available from Siltech Corp. under the trade name SILMER UR-5050, which comprises the polymer in Isododecane.
  • hydrophilic or water-soluble film former e.g., cellulosics, polysaccharides, polyquaterniums (such as polyquaternium-37 (INCI), etc.
  • a hydrophilic or water-soluble film former e.g., cellulosics, polysaccharides, polyquaterniums (such as polyquaternium-37 (INCI), etc.
  • compositions may comprise a cationic polymer.
  • Cationic polymers include, but are not limited to, polyquaternium 4, polyquaternium 6, polyquaternium 7, polyquaternium 10, polyquaternium 11, polyquaternium 16, polyquaternium 22, polyquaternium 28, polyquaternium 32, and guar hydroxypropyltrimonium chloride.
  • the cationic polymer will typically comprise an amount of about 0.1% to about 15% (w/w) of the composition.
  • the compositions may contain an amount of cationic (quaternium) ingredients that are anhydrous or have very low level of water, e.g., less than 1% by weight.
  • quaternium compounds include, without limitation, Polyquaternium-37 (INCI), Silicone Quaternium-18 (INCI), PEG-2 Dimeadowfoamamidoethylmonium Methosulfate and Hexylene Glycol (INCI), and Cetrimonium Chloride (INCI), to name a few.
  • Such quaternium compounds if present, will typically comprise from about 0.05% to about 5% by weight of the total composition, and more typically, from about 0.1% to about 1.5% by weight.
  • compositions may also comprise monomer quaternary ammonium compounds such as, for example, alkyltrimethylammonium chlorides, dialkylmethyl-ammonium chlorides, alkyldimethylbenzylammonium chlorides, and alkylpyridinium chlorides.
  • monomer quaternary ammonium compounds such as, for example, alkyltrimethylammonium chlorides, dialkylmethyl-ammonium chlorides, alkyldimethylbenzylammonium chlorides, and alkylpyridinium chlorides.
  • the composition comprises at least one hair conditioning agent selected from the group consisting of polyquaterniums, cationic polymers, cationic surfactants, non-volatile dimethicone oils, dimethiconols, amodimethicones, ester oils, fatty alcohols, cationic gums and cellulosics, amidoamines, cetrimonium chloride, behentrimonium chloride, stearamidopropyl dimethylamine, polyesteramines, and cationically charge-modified polymers derived from guar gum, cellulose, proteins, polypeptides, chitosan, lanolin, starches and amino silicones.
  • hair conditioning agent selected from the group consisting of polyquaterniums, cationic polymers, cationic surfactants, non-volatile dimethicone oils, dimethiconols, amodimethicones, ester oils, fatty alcohols, cationic gums and cellulosics, amidoamines, ce
  • compositions may include a nonionic surfactant such as Laureth-23, Ceteth-10, Ceteth-20, IsoCeteth-20, Steareth-20, Oleth-10, Oleth-20, or alkyl polyglucose.
  • the nonionic surfactant may be formed from a fatty alcohol, a fatty acid, or a glyceride with a C8 to C24 carbon chain.
  • compositions of the invention can further comprise proteins, peptides, and amino acids including hydrolyzed soy protein, lauryldimonium hydrolyzed soy protein (cationic Soya protein), wheat amino acids, corn, wheat, milk, or silk proteins, collagens, keratins, taurine and arginine hydrochloride, etc.
  • proteins, peptides, and amino acids including hydrolyzed soy protein, lauryldimonium hydrolyzed soy protein (cationic Soya protein), wheat amino acids, corn, wheat, milk, or silk proteins, collagens, keratins, taurine and arginine hydrochloride, etc.
  • the composition may also comprise polyols (e.g., glycols), such as glycerin, propylene glycol, ethoxydiglycol, glycerin, butylene glycol, pentylene glycol, hexylene glycol, caprylyl glycol, and the like. These will typically be added in amount from about 0.001 to about 5% by weight.
  • polyols e.g., glycols
  • glycols such as glycerin, propylene glycol, ethoxydiglycol, glycerin, butylene glycol, pentylene glycol, hexylene glycol, caprylyl glycol, and the like.
  • compositions may further include an emulsifier.
  • the amount of emulsifier will typically be from about 0.001 to about 10% by weight, but preferably will range from about 0.01 to about 5% by weight, and most preferably about 0.1 to about 1% by weight, based upon the total weight of the composition.
  • the emulsifier may be of the polyethoxylated type (e.g., polyoxyethylene ethers or esters) comprising chains of the form —(CH 2 CH 2 O) n —.
  • polyethoxylated emulsifiers are also contemplated to be suitable.
  • Emulsifiers that can be used in the composition of the present invention include, but are not limited to, one or more of the following: sorbitan esters; polyglyceryl-3-diisostearate; sorbitan monostearate, sorbitan tristearate, sorbitan sesquioleate, sorbitan monooleate; glycerol esters such as glycerol monostearate and glycerol monooleate; polyoxyethylene phenols such as polyoxyethylene octyl phenol and polyoxyethylene nonyl phenol; polyoxyethylene ethers such as polyoxyethylene cetyl ether and polyoxyethylene stearyl ether; polyoxyethylene glycol esters; polyoxyethylene sorbitan esters; dimethicone copolyols; polyglyceryl esters such as polyglyceryl-3-diisostearate; glyceryl laurate; Steareth-2, Steareth-10, and Steareth-20, to name
  • Water-in-silicone emulsions are typically emulsified with a nonionic surfactant (emulsifier).
  • emulsifiers include polydiorganosiloxane-polyoxyalkylene block copolymers, including those described in U.S. Pat. No. 4,122,029, the disclosure of which is hereby incorporated by reference.
  • emulsifiers generally comprise a polydiorganosiloxane backbone, typically polydimethylsiloxane, having side chains comprising -(EO) m — and/or —(PO) n — groups, where EO is ethyleneoxy and PO is 1,2-propyleneoxy, the side chains being typically capped or terminated with hydrogen or lower alkyl groups (e.g., C 1-6 , typically C 1-3 ).
  • the silicone emulsifier may also comprise alkyl chains pendant from the silicone backbone.
  • Other suitable water-in-silicone emulsifiers are disclosed in U.S. Pat. No.
  • water-in-silicone emulsifiers include those available from Dow Corning under the trade designations 3225C and 5225C FORMULATION AID; SILICONE SF-1528 available from General Electric; ABIL EM 90 and EM 97, available from Goldschmidt Chemical Corporation (Hopewell, Va.); and the SILWETTM series of emulsifiers sold by OSI Specialties (Danbury, Conn.).
  • water-in-silicone emulsifiers include, but are not limited to, dimethicone PEG 10/15 crosspolymer, dimethicone copolyol, cetyl dimethicone copolyol, PEG-15 lauryl dimethicone crosspolymer, laurylmethicone crosspolymer, cyclomethicone and dimethicone copolyol, dimethicone copolyol (and) caprylic/capric triglycerides, polyglyceryl-4 isostearate (and) cetyl dimethicone copolyol (and) hexyl laurate, and dimethicone copolyol (and) cyclopentasiloxane.
  • water-in-silicone emulsifiers include, without limitation, PEG/PPG-18/18 dimethicone (trade name 5225C, Dow Corning), PEG/PPG-19/19 dimethicone (trade name BY25-337, Dow Corning), Cetyl PEG/PPG-10/1 dimethicone (trade name Abil EM-90, Goldschmidt Chemical Corporation), PEG-12 dimethicone (trade name SF 1288, General Electric), lauryl PEG/PPG-18/18 methicone (trade name 5200 FORMULATION AID, Dow Corning), PEG-12 dimethicone crosspolymer (trade name 9010 and 9011 silicone elastomer blend, Dow Corning), PEG-10 dimethicone crosspolymer (trade name KSG-20, Shin-Etsu), and dimethicone PEG-10/15 crosspolymer (trade name KSG-210, Shin-Etsu).
  • PEG/PPG-18/18 dimethicone trade name 5225C,
  • compositions of the invention will typically have a pH ranging from 2-12, more typically from 2 to 10. In some embodiments, the compositions will have a pH ranging from about 3 to about 7, or from about 3.5 to about 6.5.
  • the pH may be adjusted using conventionally acid or base pH adjusters including, without limitation, citric acid, mineral acids, ethanolamine and other amines, ammonia, sodium hydroxide, etc.
  • the shine-enhancing agent may be, for example, lens-shaped particles such as hemi-spherical PMMA, including the hemi-spherical methyl methacrylate crosspolymer sold under the trade name 3D Tech PW (Plain) XP (Kobo).
  • suitable shine enhancers include phenylpropyldimethylsiloxysilicate, polybutene, polyisobutene, hydrogenated polyisobutene. Silicone fluids, such as aryl-substituted siloxanes having high refractive indices are also useful as shine enhancers.
  • Phenyltrimethicone which is available under the trade names SCI-TEC PTM 100 (ISP) and PDM20 (Wacker-Belsil), and Trimethylsiloxyphenyl Dimethicone (INCI name), which is available under the trade name PDM 1000 (Wacker-Belsil).
  • the PDM20 material has a refractive index of 1.437 at 25° C.
  • the PDM 1000 material has a refractory index of 1.461 at 25° C.
  • Another suitable silicone fluid may be trimethylsiloxyphenyl dimethicone.
  • any aryl-substituted silicone having a refractive index of greater than 1.4 at 25° C.
  • Phenyl silicones such as pentaphenyl trimethyl trisiloxane or tetraphenyl tetramethyl trisiloxane, commercially available as HRI fluids from Dow corning HRI, are also useful for enhancing shine.
  • Certain organic compounds, such as octyl methoxy cinnamate, may also be used to enhance shine.
  • the shine enhancer is typically present from about 0.01% to about 5% by weight of the total composition.
  • compositions according to the invention may comprise pigments, pearlescents, and/or colorants to impart a desired color to the hair.
  • Inorganic pigments include without limitation titanium dioxide, zinc oxide, iron oxides, chromium oxide, ferric blue, and mica; organic pigments include barium, strontium, calcium or aluminum lakes, ultramarines, and carbon black; colorants include without limitation D&C Green #3, D&C Yellow #5, and D&C Blue #1.
  • Pigments and/or colorants may be coated or surface treated with one or more compatibilizers to aid in dispersion in the solvent. Preferred pigments and/or colorants are those surface treated to render them hydrophobic.
  • compositions of the invention may optionally comprise other active and inactive ingredients typically associated with hair care products.
  • the nature of these other ingredients and their amounts should preferably be suitable for formulating a stable hair care product which forms a film on keratin fibers.
  • these other ingredients include at least one bioactive ingredient for improving the keratin fiber.
  • Suitable other ingredients include, but are not limited to, amino acids, antioxidants, chelating agents, colorants, emollients, emulsifiers, excipients, fillers, fragrances, gelling agents, humectants, minerals, moisturizers, photostabilizing agents (e.g., UV absorbers), preservatives, stabilizers, staining agents, surfactants, viscosity and/or rheology modifiers, vitamins, waxes and mixtures thereof. It is contemplated that the inventive hair care product of the present invention can also include anti-dandruff, deodorant, sunscreen and/or antiperspirant ingredients. Collectively, all such additional components usually will comprise less than 10% by weight of the composition.
  • compositions typically comprises a preservative or anti-microbial agent, for example, methylchloroisothiazolinone, methylisothiazolinone, methylparaben, propylparaben, phenoxyethanol, or caprylyl glycol.
  • a preservative or anti-microbial agent for example, methylchloroisothiazolinone, methylisothiazolinone, methylparaben, propylparaben, phenoxyethanol, or caprylyl glycol.
  • composition of the present invention may be formulated in any suitable form, including various rinse-off and leave-in formulations, such as but not limited to shampoos, conditioners, serums, creams, sprays, emulsions, gels, balms, liquids, and the like.
  • a leave-in conditioner comprises from 0.1 to about 2.5% by weight of a compound of Formula (I) (e.g., TDPA), from about 1% to about 97% by weight of a vehicle, and from about 0.01% to about 15% by weight (collectively) of one or more of the following: a conditioning agent, a thickener, an anionic, cationic, zwitterionic, or non-ionic surfactant, dimethicone oil, polyquaternium-37, panthenol, panthenyl ethyl ether, hydrogenated castor oil/sebacic acid copolymer, wheat amino acids, phytantriol, tocopheryl acetate, vinyl dimethicone/lauryl dimethicone crosspolymer, propylene glycol dicaprylate/dicaprate, phenoxyethanol, hydroxyethylcellulose, caprylyl glycol, PPG-1 Ttrideceth-6, and quaternium-80.
  • a conditioning agent e.
  • a rinse off conditioner comprises from 0.1 to about 2.5% by weight of a compound of Formula (I) (e.g., TDPA), from about 1% to about 97% by weight of a vehicle, and from about 0.01% to about 15% by weight (collectively) of one or more of the following: a conditioning agent, a thickener, an anionic, cationic, zwitterionic, or non-ionic surfactant, cetyl alcohol, dimethiconol, cetearyl alcohol, stearamidopropyl dimethylamine, cetrimonium chloride, butylene glycol, glycol stearate, wheat amino acids, panthenyl ethyl ether, phytantriol, hydrogenated castor oil/sebacic acid copolymer, tocopheryl acetate, panthenol, vinyl dimethicone/lauryl/behenyl dimethicone crosspolymer, ceteareth-20, glycolic acid, and polyethylene glycol (including P
  • a shampoo comprises from 0.1 to about 2.5% by weight of a compound of Formula (I) (e.g., TDPA), from about 1% to about 97% by weight of a vehicle, and from about 0.01% to about 15% by weight (collectively) of one or more of the following: a conditioning agent, a thickener, an anionic, cationic, zwitterionic, or non-ionic surfactant, lauryl glucoside, sodium laureth sulfate, cocamide MIPA, sodium lauroyl sarcosinate, glycol distearate, dimethicone, wheat amino acids, panthenyl ethyl ether, phytantriol, hydrogenated castor oil/sebacic acid copolymer, tocopheryl acetate, panthenol, vinyl dimethicone/lauryl/behenyl dimethicone crosspolymer, PEG-150 pentaerythrityl tetrastearate,
  • compositions are advantageously applied to hair in need thereof, by which is meant hair that has been damaged, such as hair damaged by chemical (color treatments, perms, etc.), thermal (blow dryers, curling irons, etc.), or mechanical (combing and brushing, etc.) insults. Hair in need thereof may also include hair that is damaged by UV light and swimming pool chemicals.
  • the composition is applied to hair that has been previously artificially colored, for example, with a two-part oxidative dye.
  • compositions are typically applied to wet hair, or to damp hair (such as hair that has been towel-dried), or to dry hair.
  • the composition may be left on the hair, meaning that after application no immediate (e.g., within an hour of application) steps are taken to remove the composition (other than allowing volatile constituents to evaporate).
  • the compositions may also be other rinse-off variety, including shampoos and conditioners, which are intended to be removed substantially contemporaneous with their application (e.g., within 30 minutes).
  • Other products including pomades, hair gels and mousses, sprays, and the like are also contemplated.
  • compositions are typically applied for a time sufficient to improve the strength or overall appearance of the hair. This typically entails application daily for at least three days, at least five days, at least, one week, or at least two weeks, although it is expected that results may be seen after one use.
  • the compositions are applied to damp hair after (e.g., within 30 minutes) of shampooing.
  • the compositions are applied to damp hair after (e.g., within 30 minutes) of dying the hair, including with a two part oxidative dye.
  • This Example demonstrates that TDPA repairs damaged hair fibers as evidenced by an improvement in the tensile breaking strength of hair fibers treated with TDPA.
  • a commercial rinse-off conditioner formulation was used as a control vehicle for the study.
  • An active formulation was prepared by adding 1% (w/w) of TDPA to the control vehicle.
  • Three samples of treated hair were prepared: untreated, treatment with the control vehicle, and treatment with the control vehicle plus 1% TDPA. The treatments were applied to hair tresses that had been previously damaged by artificially color with an oxidative dye. The treatments were repeated five times.
  • the overall condition of the hair fibers was determined by measuring the tensile load required to break the fibers and the results of 30 fibers were averaged. The results are shown in FIG. 1 .
  • Control Vehicle Formula DEMINERALIZED WATER BUTYLENE GLYCOL PANTHENOL-DL METHYLPARABEN CETRIMONIUM CHLORIDE/ISOPROPANOL PEG-90M CETYL ALCOHOL CETEARYL ALCOHOL/CETEARETH-20 STEARAMIDOPROPYL DIMETHYLAMINE ETHYLENE GLYCOL MONOSTEARATE PROPYLPARABEN WHEAT AMINO ACIDS-AQ.
  • Control Vehicle Formula + 1% TDPA DEMINERALIZED WATER BUTYLENE GLYCOL PANTHENOL-DL METHYLPARABEN CETRIMONIUM CHLORIDE/ISOPROPANOL PEG-90M CETYL ALCOHOL CETEARYL ALCOHOL/CETEARETH-20 STEARAMIDOPROPYL DIMETHYLAMINE ETHYLENE GLYCOL MONOSTEARATE PROPYLPARABEN WHEAT AMINO ACIDS-AQ.
US14/354,827 2013-03-07 2014-02-27 Compositions and Methods for Treating Damaged Hair Abandoned US20150050230A1 (en)

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US14/354,827 US20150050230A1 (en) 2013-03-07 2014-02-27 Compositions and Methods for Treating Damaged Hair
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CA2899426A1 (fr) 2014-09-12
BR112015017837A2 (pt) 2017-07-11
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US20180116935A1 (en) 2018-05-03
CN105007985A (zh) 2015-10-28
US10874598B2 (en) 2020-12-29
PL2964334T3 (pl) 2021-10-25
EP2964334B1 (fr) 2021-04-07
EP2964334A1 (fr) 2016-01-13
WO2014137739A1 (fr) 2014-09-12
EP2964334A4 (fr) 2016-10-12
BR112015017837B1 (pt) 2020-08-11
HK1213523A1 (zh) 2016-07-08

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