WO1996021425A1 - Cleansing compositions - Google Patents

Cleansing compositions Download PDF

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Publication number
WO1996021425A1
WO1996021425A1 PCT/US1995/000607 US9500607W WO9621425A1 WO 1996021425 A1 WO1996021425 A1 WO 1996021425A1 US 9500607 W US9500607 W US 9500607W WO 9621425 A1 WO9621425 A1 WO 9621425A1
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WO
WIPO (PCT)
Prior art keywords
composition according
weight
oil
nonionic
cationic
Prior art date
Application number
PCT/US1995/000607
Other languages
French (fr)
Inventor
Frances Sophia Farrelly
Michel Joseph Giret
Christopher David Leahy
Original Assignee
The Procter & Gamble Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to GB9323283A priority Critical patent/GB2283754B/en
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to PCT/US1995/000607 priority patent/WO1996021425A1/en
Priority to JP8521624A priority patent/JPH10512254A/en
Priority to EP95908533A priority patent/EP0794766A4/en
Publication of WO1996021425A1 publication Critical patent/WO1996021425A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • 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
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/27Zinc; Compounds 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides 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
    • 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
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817Compositions 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)
    • A61K8/8182Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • 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
    • 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
    • A61K2800/54Polymers characterized by specific structures/properties
    • A61K2800/542Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5422Polymers characterized by specific structures/properties characterized by the charge nonionic
    • 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
    • A61K2800/54Polymers characterized by specific structures/properties
    • A61K2800/542Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5426Polymers characterized by specific structures/properties characterized by the charge cationic

Definitions

  • the present invention relates to cleansing compositions.
  • mild personal cleansing compositions with good skin feel attributes and foaming properties suitable for simultaneously cleansing and conditioning the skin and/or the hair and which may be used, for example, in the form of foam bath preparations, shower products, skin cleansers, hand, face and body cleansers, shampoos, etc.
  • Mild cosmetic compositions must satisfy a number of criteria including cleansing power, foaming properties and mildness/low irritancy/good feel with respect to the skin, hair and the ocular mucosae.
  • Skin is made up of several layers of cells which coat and protect the keratin and collagen fibrous proteins that form the skeleton of its structure. The outermost of these layers, referred to as the stratum corneum, is known to be composed of 250 A protein bundles surrounded by 80 A thick layers. Hair similarly has a protective outer coating enclosing the hair fibre which is called the cuticle.
  • Anionic surfactants can penetrate the stratum corneum membrane and the cuticle and, by delipidization destroy membrane integrity. This interference with skin and hair protective membranes can lead to a rough skin feel and eye irritation and may eventually permit the surfactant to interact with the keratin and hair proteins creating irritation and loss of barrier and water retention functions.
  • Ideal cosmetic cleansers should cleanse the skin or hair gently, without defatting and/or drying the hair and skin and without irritating the ocular mucosae or leaving skin taut after frequent use.
  • Most lathering soaps, shower and bath products, shampoos and bars fail in this respect.
  • Certain synthetic surfactants are known to be mild.
  • a major drawback of most mild synthetic surfactant systems when formulated for shampooing or personal cleansing is poor lather performance compared to the highest shampoo and bar soap standards.
  • surfactants that are among the mildest such as sodium lauryl glyceryl ether sulfonate, (AGS), are marginal in lather.
  • the subject of the present invention is a mild, foam-producing cleansing product suitable for personal cleansing of the skin or hair and which may be used as foam bath and shower products, skin cleansers and shampoos etc.
  • a liquid personal cleansing composition comprising:
  • surfactant selected from anionic, nonionic, zwitterionic and amphoteric surfactants and mixtures thereof;
  • the invention takes the form of a foam producing liquid cleansing composition with superior skin feel and rinsing characteristics, improved perceived dryness and assessed tightness and expertly graded dryness, combined with excellent lathering, good stability, cleansing ability and conditioning performance.
  • the liquid cleansing compositions herein are based on a combination of mild surfactants with certain water-insoluble fatty acid metal salts.
  • Preferred embodiments also contain polymeric skin conditioning agents and/or perfume or cosmetic oils.
  • Water- insoluble fatty acid salt suitable for use hererin include zinc, magnesium, calcium, lithium, and aluminium salts of C14-C22, preferably C16- 18 fatty acids, and mixtures thereof.
  • Highly preferred from the viewpoint of optimum skin feel and conditioning effectiveness are the zinc salts, especially zinc salts of Cj ⁇ -Cis fatty acids which are marketed under the designation zinc stearate.
  • the water-insoluble fatty acid salts are especially valuable in combination with cationic or nonionic polymeric skin conditioning agents for providing improved skin conditioning as well as skin feel attributes typical of soap-based cleansing products.
  • the total level of fatty acid metal salt is from about 0.1 % to about 5 % , preferably 0.2% to about 3%, more preferably from about 0.5% to about 2% by weight of composition,
  • compositions according to the present invention also include in preferred embodiments a skin conditioning cationic or nonionic polymer.
  • the polymeric skin conditioning agent is preferably present at a level from about 0.01 % to about 5%, preferably from about 0.05% to about 3% and especially from about 0.1% to about 2% by weight.
  • Suitable polymers are high molecular weight materials (mass- average molecular weight determined, for instance, by light scattering, being generally from about 2,000 to about 5,000,000, preferably from about 5,000 to about 3,000,000 more preferably from 100,000 to about 1,000,000).
  • Representative classes of polymers include cationic and nonionic polysaccharides; cationic and nonionic homopolymers and copolymers derived from acrylic and/or methacrylic acid; cationic and nonionic cellulose resins; cationic copolymers of dimethyldiallylammonium chloride and acrylamide and or acrylic acid; cationic homopolymers of dimethyldiallylammonium chloride; cationic polyalkylene and ethoxypolyalkylene imines; quaternized silicones, and mixtures thereof.
  • cationic polymers suitable for use herein include cationic guar gums such as hydroxypropyl trimethyl ammonium guar gum (d.s. of from 0.11 to 0.22) available commercially under the trade names Jaguar C-14-S(RTM) and Jaguar C-17(RTM) and also Jaguar C-16(RTM), which contains hydroxypropyl substituents (d.s. of from 0.8- 1.1) in addition to the above-specified cationic groups, and quaternized cellulose ethers available commercially under the trade names Ucare Polymer JR-30M, JR-400 and Celquat.
  • quaternized cellulose ethers available commercially under the trade names Ucare Polymer JR-30M, JR-400 and Celquat.
  • Suitable cationic polymers are homopolymers of dimethyldiallylammonium chloride available commercially under the trade name Merquat 100, copolymers of dimethyl aminoethylmethacrylate and acrylamide, copolymers of dimethyldiallylammonium chloride and acrylamide, available commercially under the trade names Merquat 550 and Merquat S, acrylic acid/dimethyldiallylammonium chloride/acrylamide copolymers available under the trade name Merquat 3300, quaternized vinyl pyrrolidone aery late or methacrylate copolymers of amino alcohol available commercially under the trade name Gafquat, for example Polyquatemium 11 , 23 and 28 (quaternized copolymers of vinyl pyrrolidone and dimethyl aminoethylmethacrylate - Gafquat 755N and HS-100), vinyl pyrrolidone/vinyl imidazolium methochloride copolymers available under the trade names Luviquat
  • the weight ratio of water-insoluble metal salt: polymeric skin conditioning agent is in the range from about 50:1 to about 1 :10.
  • Mild surfactants suitable for inclusion in compositions according to the present invention can be selected from anionic, nonionic, amphoteric and zwitterionic surfactants and mixtures thereof.
  • the total level of surfactant is preferably from about 5% to about 60%, more preferably from about 8% to about 40%, and especially from about 10% to about 35% by weight.
  • the compositions preferably comprise a mixture of anionic with zwitterionic and/or amphoteric surfactants.
  • the level of the individual anionic, zwitterionic and amphoteric surfactant components, where present, is in the range from about 1 % to about 15%, and especially from about 2% to about 13% by weight of the composition, while the level of nonionic surfactant, where present, is in the range from about 0.1 % to about 20% by weight, preferably from about 2% to about 16%, more preferably from about 3% to about 12% by weight.
  • the total level of anionic, amphoteric, and zwitterionic surfactant components is preferably from about 5% to about 50%, more preferably from about 8% to about 35% and especially from about 10% to about 30% by weight of composition.
  • the weight ratio of anionic surfactant: zwitterionic and/or amphoteric surfactant is in the range from about 1:2 to about 6:1.
  • Other suitable compositions within the scope of the invention comprise mixtures of anionic, zwitterionic and/or amphoteric surfactants with one or more nonionic surfactants.
  • Preferred for use herein are soluble or dispersible nonionic surfactants selected from ethoxylated animal and vegetable oils and fats and mixtures thereof, sometimes referred to herein as "oil- derived" nonionic surfactants.
  • Anionic surfactants suitable for inclusion in the compositions of the invention can generally be described as mild synthetic detergent surfactants and include ethoxylated alkyl sulfates, alkyl glyceryl ether sulfonates, methyl acyl taurates, fatty acyl glycinates, N-acyl glutamates, acyl isethionates, alkyl sulfosuccinates, alpha-sulfonated fatty acids, their salts and/or their esters, alkyl ethoxy carboxylates, alkyl phosphate esters, ethoxylated alkyl phosphate esters, acyl sarcosinates and fatty acid/protein condensates, and mixtures thereof.
  • Alkyl and/or acyl chain lengths for these surfactants are Cg-C22 » preferably C10-C18 more preferably
  • Preferred for use herein from the viewpoint of optimum mildness and lathering characteristics are the salts of sulfuric acid esters of the reaction product of 1 mole of a higher fatty alcohol and from about 1 to about 12 moles of ethylene oxide, with sodium and magnesium being the preferred counterions.
  • Particularly preferred are the alkyl sulfates containing from about 2 to 6, preferably 2 to 4 moles of ethylene oxide, such as sodium laureth-2 sulfate, sodium laureth-3 sulfate and magnesium sodium laureth-3.6 sulfate.
  • the anionic surfactant contains at least about 50%, especially at least about 75% by weight of ethoxylated alkyl sulfate.
  • the compositions for use herein suitably also contain an amphoteric surfactant.
  • Amphoteric surfactants suitable for use in the compositions of the invention include:
  • Ri is C7-C22 alkyl or alkenyl
  • R2 is hydrogen or CH2Z
  • each Z is independently CO2M or CH2CO2M
  • M is H, alkali metal, alkaline earth metal, ammonium or alkanolammonium; and/or ammonium derivatives of formula (ID
  • n, m, p, and q are numbers from 1 to 4, and Rj and
  • Suitable amphoteric surfactants of type (a) are marketed under the trade name Miranol and Empigen and are understood to comprise a complex mixture of species.
  • Miranols have been described as having the general formula I, although the CTFA Cosmetic Ingredient Dictionary, 3rd Edition indicates the non-cyclic structure II while the 4th Edition indicates yet another structural isomer in which R2 is
  • amphoteric surfactants of type (a) include compounds of formula I and/or II in which R ⁇ is CgH ⁇ (especially iso- capryl), C9H19 and C11H23 alkyl.
  • R ⁇ is CgH ⁇ (especially iso- capryl), C9H19 and C11H23 alkyl.
  • R ⁇ is CgH ⁇ (especially iso- capryl), C9H19 and C11H23 alkyl.
  • R ⁇ is CgH ⁇ (especially iso- capryl), C9H19 and C11H23 alkyl.
  • R ⁇ is CgH ⁇ (especially iso- capryl), C9H19 and C11H23 alkyl.
  • Ri is C9H19, Z is CO2M and R2 is H
  • the compounds in which Ri is C11H23, Z is CO2M and R2 is CH2CO2M
  • R ⁇ is C11H23, Z is CO2M and R2 is H.
  • materials suitable for use in the present invention include cocoamphocarboxypropionate, cocoamphocarboxy prop ionic acid, and especially cocoamphoacetate and cocoamphodiacetate (otherwise referred to as cocoamphocarboxyglycinate).
  • Specific commercial products include those sold under the trade names of Ampholak 7TX (sodium carboxy methyl tallow polypropyl amine), Empigen CDL60 and CDR 60 (Albright & Wilson), Miranol H2M Cone. Miranol C2M Cone. N.P., Miranol C2M Cone.
  • Miranol C2M SF Miranol CM Special (Rh ⁇ ne-Poulenc); Alkateric 2CIB (Alkaril Chemicals); Amphoterge W-2 (Lonza, Inc.); Monateric CDX-38, Monateric CSH-32 (Mona Industries); Rewoteric AM-2C (Rewo Chemical Group); and Schercotic MS-2 (Scher Chemicals).
  • amphoteric surfactants of this type are manufactured and sold in the form of electroneutral complexes with, for example, hydroxide counterions or with anionic sulfate or sulfonate surfactants, especially those of the sulfated Cg-Ci8 alcohol, Cg-Ci8 ethoxylated alcohol or C8-C ⁇ 8 acyl glyceride types.
  • anionic sulfate or sulfonate surfactants especially those of the sulfated Cg-Ci8 alcohol, Cg-Ci8 ethoxylated alcohol or C8-C ⁇ 8 acyl glyceride types.
  • compositions which are essentially free of (non- ethoxylated) sulfated alcohol surfactants are based herein on the uncomplexed forms of the surfactants, any anionic surfactant counterions being considered as part of the overall anionic surfactant component content.
  • amphoteric surfactants of type (b) include N-alkyl polytrimethylene poly-, carboxymethylamines sold under the trade names Ampholak X07 and Ampholak 7CX by Berol Nobel and also salts, especially the triethanolammonium salts and salts of N-lauryl-beta-amino propionic acid and N-lauryl-imino-dipropionic acid.
  • Such materials are sold under the trade name Deriphat by Henkel and Mirataine by Rh ⁇ ne- Poulenc.
  • compositions herein can also contain from about 0.1 % to about 20%, more preferably from about 0.1 % to about 10% , and especially from about 1 % to about 8% of a zwitterionic surfactant, especially an alkyl betaine or amidobetaine surfactant.
  • Betaine surfactants suitable for inclusion in the composition of the invention include alkyl betaines of the formula R5R-6R7N+(CH2) n C02M(VIII) and amido betaines of the formula (IX) i 6
  • R5 is C12-C22 alkyl or alkenyl
  • R$ and R7 are independently C1-C3 alkyl
  • M is H, alkali metal, alkaline earth metal, ammonium or alkanolammonium
  • n, m are each numbers from 1 to 4.
  • Preferred betaines include cocoamidopropyldimethylcarboxy methyl betaine, laurylamidopropyldimethylcarboxy methyl betaine and Tego betaine.
  • compositions of the invention preferably also contain from about 0.1 % to about 20%, preferably from about 1 % to about 15%, and more preferably from about 2% to about 10% by weight of an oil derived nonionic surfactant or mixture of oil derived nonionic surfactants.
  • Oil derived nonionic surfactants are valuable in compositions according to the invention for the provision of skin feel benefits both in use and after use.
  • Suitable oil derived nonionic surfactants for use herein include water soluble vegetable and animal-derived emollients such as triglycerides with a polyethyleneglycol chain inserted; ethoxylated mono and di-glycerides, polyethoxylated lanolins and ethoxylated butter derivatives.
  • One preferred class of oil-derived nonionic surfactants for use herein have the general formula (VI)
  • n is from about 5 to about 200, preferably from about 20 to about 100, more preferably from about 30 to about 85, and wherein R comprises an aliphatic radical having on average from about 5 to 20 carbon atoms, preferably from about 9 to 18 carbon atoms.
  • Suitable ethoxylated oils and fats of this class include polyethyleneglycol derivatives of glyceryl cocoate, glyceryl caproate, glyceryl caprylate, glyceryl tallowate, glyceryl palmate, glyceryl stearate, glyceryl laurate, glyceryl oleate, glyceryl ricinoleate, and glyceryl fatty esters derived from triglycerides, such as palm oil, almond oil, and corn oil, preferably glyceryl tallowate and glyceryl cocoate.
  • Suitable oil derived nonionic surfactants of this class are available from Croda Inc. (New York, USA) under their Crovol line of materials such as Crovol EP40 (PEG 20 evening primrose glyceride), Crovol EP 70 (PEG 60 evening primrose glyceride) Crovol A-40 (PEG 20 almond glyceride), Crovol A-70 (PEG 60 almond glyceride), Crovol M-40 (PEG 20 maize glyceride), Crovol M-70 (PEG 60 maize glyceride), Crovol PK- 40 (PEG 12 palm kernel glyceride), and Crovol PK-70 (PEG 45 palm kernel glyceride) and under their Solan range of materials such as Solan E, E50 and X polyethoxylated lanolins and Aqualose L-20 (PEG 24 lanolin alcohol) available from Westbrook Lanolin.
  • Crovol EP40 PEG 20 evening primrose glyceride
  • Crovol EP 70 PEG 60 evening primrose gly
  • Varonic LI 2 PEG 28 glyceryl tallowate
  • Varonic LI 420 PEG 200 glyceryl tallowate
  • Varonic LI 63 and 67 PEG 30 and PEG 80 glyceryl cocoates
  • nonionic surfactants derived from composite vegetable fats extracted from the fruit of the Shea Tree (Butyrospermum Karkii Kotschy) and derivatives thereof.
  • This vegetable fat known as Shea Butter is widely used in Central Africa for a variety of means such as soap making and as a barrier cream, it is marketed by Sederma (78610 Le Perray En Yvelines, France).
  • Particularly suitable are ethoxylated derivatives of Shea butter available from Karlshamn Chemical Co. (Columbos, Ohio, USA) under their Lipex range of chemicals, such as Lipex 102 E-75 (ethoxylated mono, di-glycerides of Shea butter).
  • ethoxylated derivatives of Mango, Cocoa and Illipe butter may be used in compositions according to the invention. Although these are classified as ethoxylated nonionic surfactants it is understood that a certain proportion may remain as non-ethoxylated vegetable oil or fat.
  • suitable oil-derived nonionic surfactants include ethoxylated derivatives of almond oil, peanut oil, rice bran oil, wheat germ oil, linseed oil, jojoba oil, oil of apricot pits, walnuts, palm nuts, pistachio nuts, sesame seeds, rapeseed, cade oil, com oil, peach pit oil, poppyseed oil, pine oil, castor oil, soybean oil, avocado oil, safflower oil, coconut oil, hazlenut oil, olive oil, grapeseed oil, and sunflower seed oil.
  • Oil derived nonionic surfactants highly preferred for use herein from the viewpoint of optimum mildness and skin feel characteristics are PEG 60 evening primrose triglycerides; PEG 55 lanolin polyethoxylated derivatives and ethoxylated derivatives of Shea butter.
  • compositions of the invention can also comprise an auxiliary nonionic surfactant at levels from about 0.1 % to about 20%, more preferably from about 0.1 % to about 10%, and especially from about 1 % to about 8% by weight.
  • auxiliary nonionic surfactant at levels from about 0.1 % to about 20%, more preferably from about 0.1 % to about 10%, and especially from about 1 % to about 8% by weight.
  • surfactants of this class include C12-C14 fatty acid mono-and diethanolamides, sucrose polyester surfactants and polyhydroxy fatty acid amide surfactants having the general formula (VII).
  • the preferred polyhydroxy fatty acid amide surfactants are those in which R9 is C ⁇ _4 alkyl, preferably methyl, and R8 is C7-C19 alkyl or alkenyl, more preferably straight-chain C9-C17 alkyl or alkenyl, or mixture thereof; and Z2 is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative (preferably ethoxylated or propoxylated) thereof.
  • Z2 preferably will be derived from a reducing sugar in a reductive amination reaction; more preferably Z2 is a glycityl.
  • Suitable reducing sugars include glucose, fructose, maltose, lactose, galactose, mannose, and xylose.
  • high dextrose com syrup, high fructose com syrup, and high maltose com syrup can be utilized as well as the individual sugars listed above. These com syrups may yield a mix of sugar components for Z2- It should be understood that it is by no means intended to exclude other suitable raw materials.
  • Z2 preferably will be selected from the group consisting of -CH2(CHOH) n - CH2 ⁇ H,-CH(CH2 ⁇ H)-(CHOH) n . ⁇ -CH2 ⁇ H, -CH2- (CHOH)2(CHOR')(CHOH)-CH2 ⁇ H, where n is an integer from 3 to 5, inclusive, and R' is H or a cyclic or aliphatic monosaccharide, and alkoxylated derivatives thereof. Most preferred are glycityls wherein n is 4, particularly -CH2-(CHOH)4-CH2 ⁇ H.
  • the most preferred polyhydroxy fatty acid amide has the formula Rg(CO)N(CH3)CH2(CHOH)4CH2 ⁇ H wherein R% is a C11-C17 straight chain alkyl or alkenyl group.
  • compositions of the invention may also contain from about 0.1 % to about 8%, preferably from about 0.5% to about 6%, and especially from about 1.5% to about 5% by weight of saturated acyl fatty acids having a weight average chain length of from 10 to 18, preferably from 12 to 16 carbon atoms. Highly preferred is myristic acid.
  • compositions of the invention may also include an insoluble perfume or cosmetic oil or wax or a mixture thereof at a level up to about 10% , preferably up to about 3% by weight wherein the oil or wax is insoluble in the sense of being insoluble in the product matrix at a temperature of 25 °C.
  • Addition of such oils or waxes can provide emolliency, mildness and rinsibility characteristics to personal cleansing compositions according to the invention. It is a feature of the invention, however, that compositions having excellent emolliency and mildness together with desirable physical attributes (clarity etc.) can be delivered which are essentially oil-free, ie which contain less than about 1 % , preferably less than 0.5% by weight of an added oil phase.
  • compositions of this type take the form of an optically-clear solution or microemulsion.
  • compositions including an additional perf ime or cosmetic oil or wax preferably the weight ratio of oil-derived nonionic surfactant to added oil is at least about 1 :2, more especially at least about 3:1.
  • Suitable insoluble cosmetic oils and waxes for use herein can be selected from water-insoluble silicones inclusive of non-volatile polyalkyl and polyaryl siloxane gums and fluids, volatile cyclic and linear polyalkylsiloxanes, polyalkoxylated silicones, amino and quaternary ammonium modified silicones, rigid cross-linked and reinforced silicones and mixtures thereof, -C24 esters of C8-C30 fatty acids such as isopropyl myristate, myristyl myristate and cetyl ricinoleate, C -C30 esters of benzoic acid, beeswax, saturated and unsaturated fatty alcohols such as behenyl alcohol, hydrocarbons such as mineral oils, petrolatum squalane and squalene, polybutene, fatty sorbitan esters (see US-A- 3988255, Seiden, issued October 26th 1976), lanolin and oil-like lanolin derivatives, animal and
  • the viscosity of the final composition (Brookfield RVT DCP, 1 rpm with Cone CP41 or CP52, 25 °C, neat) is preferably at least about 500 cps, more preferably from about 1 ,000 to about 50,000 cps, especially from about 5,000 to about 30,000 cps, the viscosity being controlled using conventional hydrophilic gelling agents and thickeners.
  • compositions of the invention thus can also contain a hydrophilic gelling agent at a level preferably from about 0.01 % to about 10%, more preferably from about 0.02% to about 2%, and especially from about 0.02% to about 0.5%.
  • the gelling agent preferably has a viscosity (1 % aqueous solution, 20°C, Brookfield RVT) of at least about 4000 mPa.s, more preferably a least about 10,000 mPa.s and especially at least 50,000 mPa.s.
  • hydrophilic gelling agents can generally be described as water-soluble or colloidally water-soluble polymers, and include cellulose ethers (e.g. hydroxyethyl cellulose, methyl cellulose, hydroxypropylmethyl cellulose), polyvinylpyrrolidone, polyvinylalcohol, guar gum, hydroxpropyl guar gum and xanthan gum.
  • cellulose ethers e.g. hydroxyethyl cellulose, methyl cellulose, hydroxypropylmethyl cellulose
  • polyvinylpyrrolidone e.g. hydroxyethyl cellulose, methyl cellulose, hydroxypropylmethyl cellulose
  • polyvinylalcohol e.g. hydroxyethyl cellulose, methyl cellulose, hydroxypropylmethyl cellulose
  • guar gum e.g. hydroxypropyl guar gum
  • hydroxpropyl guar gum e.g. xanthan gum
  • Preferred hydrophilic gelling agents herein are acrylic acid/ethyl acrylate copolymers and the carboxyvinyl polymers sold by the B.F. Goodrich Company under the trade mark of Carbopol resins. These resins consist essentially of a colloidally water-soluble polyalkenyl polyether crosslinked polymer of acrylic acid crosslinked with from 0.75% to 2.00% of a crosslinked agent such as for example polyallyl sucrose or polyallyl pentaerythritol. Examples include Carbopol 934, Carbopol 940, Carbopol 950, Carbopol 980, Carbopol 951 and Carbopol 981.
  • Carbopol 934 is a water-soluble polymer of acrylic acid crosslinked with about 1 % of a polyallyl ether of sucrose having an average of about 5.8 allyl groups for each sucrose molecule.
  • a most preferred polymer is Carbopol 951.
  • a combination of the polyalkenyl polyether cross-linked acrylic acid polymer and hydrophobically modified cross-linked acrylic acid polymer is also suitable for use herein.
  • the gelling agents herein are particularly valuable for providing excellent stability characteristics over both normal and elevated temperatures.
  • Neutralizing agents suitable for use in neutralizing acidic group contining hydrophilic gelling agents herein include sodium hydroxide, potasssium hydroxide, ammonium hydroxide, monoethanoiamine, diethanolamine and triethanolamine.
  • the cleansing compositions can optionally include other hair or skin moisturizers which are soluble in the cleansing composition matrix.
  • the preferred level of such moisturizers is from about 0.5% to about 20% by weight.
  • the moisturizer is selected from:
  • nonocclusive moisturizers are polybutene, squalane, glycerine, polyethylene glycol, propylene glycol, sorbitol, polyethylene glycol and propylene glycol ethers of methyl glucose (e.g. ethyl glucam E-20 and propylglucan P-10), polyethylene glycol and propylene glycol ethers of lanolin alcohol (e.g. Solulan-75), sodium pyrrolidone carboxylic acid, lactic acid, L-proline, guanidine, pyrrolidone, hydrolyzed protein and other collagen-derived proteins, aloe vera gel and acetamide MEA and mixtures thereof.
  • glycerine is highly preferred.
  • a number of additional optional materials can be added to the cleansing compositions each at a level of from about 0.1 % to about 2% by weight.
  • Such materials include proteins and polypeptides and derivatives thereof; water-soluble or solubilizable preservatives such as DMDM Hydantoin, Germall 115, methyl, ethyl, propyl and butyl esters of hydroxybenzoic acid, EDTA, Euxyl (RTM) K400, natural preservatives such as benzyl alcohol, potassium sorbate and bisabalol; sodium benzoate and 2-phenoxyethanol; other moisturizing agents such as hyaluronic acid, chitin , and starch-grafted sodium polyacrylates such as Sanwet (RTM) IM-1000, IM-1500 and IM-2500 available from Celanese Superabsorbent Materials, Portsmith, VA, USA and described in US-A-4,076,663; solvents such as hexylene glycol and propylene glycol
  • Ti ⁇ 2-coated mica Ti ⁇ 2-coated mica; perfumes and perfume solubilizers; and zeolites such as Valfour BV400 and derivatives thereof and Ca2+/Mg2+ sequestrants such as polycarboxylates, amino polycarboxylates, polyphosphonates, amino polyphosphonates etc.
  • Water is also present at a level preferably of from about 45% to about 94% preferably at least about 60% by weight of the compositions herein.
  • the pH of the compositions is preferably from about 4 to about 10, more preferably from about 6 to about 9.
  • Solan Solan (RTM) E PEG 55 lanolin
  • Polymer 1 Polymer JR-400 - hydroxyethylcellulose reacted with epichlorohydrin and quaternized with trimethylamine, m.wt. 4 x 10 6
  • compositions in the form of shower gel or bath foam products and which are representative of the present invention:
  • Anionic 2 1.0 2.0 2.0 2.0 1.0
  • Polymer 1 0.8 1.0 - 1.0 1.0 -
  • compositions I to VI are prepared by forming a surfactant phase A at about 65 °C containing a portion of the water, the anionic, amphoteric and oil-derived nonionic surfactants and the remaining water-soluble, oil- insoluble ingredients.
  • a surfactant phase A at about 65 °C containing a portion of the water, the anionic, amphoteric and oil-derived nonionic surfactants and the remaining water-soluble, oil- insoluble ingredients.
  • an oil phase B is formed from these oil-soluble ingredients which is then admixed with A at about 65 °C and cooled to ambient temperature. Finally the remaining water, preservative and perfume are added.
  • the products provide excellent in-use and efficacy benefits including mildness, soap-like skin feel, skin conditioning, skin moisturising, stability, cleansing, lathering and rinsibility.

Abstract

A liquid personal cleansing composition comprising: a) from about 5 % to about 60 % by weight of surfactant selected from anionic, nonionic, zwitterionic and amphoteric surfactants and mixtures thereof; b) from about 0.1 % to about 5 % by weight of a water-insoluble salt of a C14-C22 fatty acid; c) optionally from about 0.01 % to about 5 % by weight of a cationic or nonionic polymeric skin conditioning agent; and d) water. The products demonstrate excellent in-use efficacy benefits including mildness, a soap-like skin feel and good product stability.

Description

CLEANSING COMPOSITIONS
TECHNICAL FIELD
The present invention relates to cleansing compositions. In particular it relates to mild personal cleansing compositions with good skin feel attributes and foaming properties suitable for simultaneously cleansing and conditioning the skin and/or the hair and which may be used, for example, in the form of foam bath preparations, shower products, skin cleansers, hand, face and body cleansers, shampoos, etc.
Background Of The Invention
Mild cosmetic compositions must satisfy a number of criteria including cleansing power, foaming properties and mildness/low irritancy/good feel with respect to the skin, hair and the ocular mucosae. Skin is made up of several layers of cells which coat and protect the keratin and collagen fibrous proteins that form the skeleton of its structure. The outermost of these layers, referred to as the stratum corneum, is known to be composed of 250 A protein bundles surrounded by 80 A thick layers. Hair similarly has a protective outer coating enclosing the hair fibre which is called the cuticle. Anionic surfactants can penetrate the stratum corneum membrane and the cuticle and, by delipidization destroy membrane integrity. This interference with skin and hair protective membranes can lead to a rough skin feel and eye irritation and may eventually permit the surfactant to interact with the keratin and hair proteins creating irritation and loss of barrier and water retention functions.
Ideal cosmetic cleansers should cleanse the skin or hair gently, without defatting and/or drying the hair and skin and without irritating the ocular mucosae or leaving skin taut after frequent use. Most lathering soaps, shower and bath products, shampoos and bars fail in this respect. Certain synthetic surfactants are known to be mild. However, a major drawback of most mild synthetic surfactant systems when formulated for shampooing or personal cleansing is poor lather performance compared to the highest shampoo and bar soap standards. Thus, surfactants that are among the mildest, such as sodium lauryl glyceryl ether sulfonate, (AGS), are marginal in lather. The use of known high sudsing anionic surfactants with lather boosters, on the other hand, can yield acceptable lather volume and quality but at the expense of clinical skin mildness. These two facts make the surfactant selection, the lather and mildness benefit formulation process a delicate balancing act.
Despite the many years of research that have been expended by the toiletries industry on personal cleansing, the broad mass of consumers remain dissatisfied by the skin feel, mildness and rinsing characteristics of present day synthetic based cleansing compositions. Many consumers prefer the skin feel and rinsing characteristics of soap cleansing products. However such soap based products cannot achieve the mildness attributes associated with mild synthetic surfactants. Moreover, a number of cationic and nonionic polymers which have been added to personal cleansing products for skin conditioning purposes are also found to be detrimental to skin feel, delivering a "slick" rather than soap-like feel on the skin.
Thus a need exists for personal cleansing products which deliver soap-like in-use skin feel characteristics but which will not dehydrate the skin or result in loss of skin suppleness, which will provide a level of skin conditioning performance in a wash and rinse-off product which previously has only been provided by a separate post-cleansing cosmetic moisturizer and which will produce a foam which is stable and of high quality, which are effective hair and skin cleansers, which have good rinsibility characteristics, and which at the same time have stable product and viscosity characteristics and remain fully stable under long term and stressed temperature storage conditions.
It has now been found that personal cleansing compositions having improved (soap-like) skin feel and moisturisation attributes, both in use and after use and good product stability can be formed by the addition thereof of certain water-insoluble salts of fatty acids.
Summary Of The Invention
The subject of the present invention is a mild, foam-producing cleansing product suitable for personal cleansing of the skin or hair and which may be used as foam bath and shower products, skin cleansers and shampoos etc. According to one aspect of the invention, there is provided a liquid personal cleansing composition comprising:
(a) from about 5% to about 60% by weight of surfactant selected from anionic, nonionic, zwitterionic and amphoteric surfactants and mixtures thereof;
(b) from about 0.1 % to 5 % by weight of a water-insoluble salt of a C] - C22 fatty acid;
(c) from about 0.01 % to about 5% by weight of cationic or nonionic polymeric skin conditioning agent; and
(d) water.
In a highly preferred embodiment, the invention takes the form of a foam producing liquid cleansing composition with superior skin feel and rinsing characteristics, improved perceived dryness and assessed tightness and expertly graded dryness, combined with excellent lathering, good stability, cleansing ability and conditioning performance.
All concentrations and ratios herein are by weight of the cleansing composition, unless otherwise specified. Surfactant chain lengths are also on a weight average chain length basis, unless otherwise specified.
The liquid cleansing compositions herein are based on a combination of mild surfactants with certain water-insoluble fatty acid metal salts. Preferred embodiments also contain polymeric skin conditioning agents and/or perfume or cosmetic oils. Water- insoluble fatty acid salt suitable for use hererin include zinc, magnesium, calcium, lithium, and aluminium salts of C14-C22, preferably C16- 18 fatty acids, and mixtures thereof. Highly preferred from the viewpoint of optimum skin feel and conditioning effectiveness are the zinc salts, especially zinc salts of Cjβ-Cis fatty acids which are marketed under the designation zinc stearate. The water-insoluble fatty acid salts are especially valuable in combination with cationic or nonionic polymeric skin conditioning agents for providing improved skin conditioning as well as skin feel attributes typical of soap-based cleansing products. The total level of fatty acid metal salt is from about 0.1 % to about 5 % , preferably 0.2% to about 3%, more preferably from about 0.5% to about 2% by weight of composition,
The compositions according to the present invention also include in preferred embodiments a skin conditioning cationic or nonionic polymer. The polymeric skin conditioning agent is preferably present at a level from about 0.01 % to about 5%, preferably from about 0.05% to about 3% and especially from about 0.1% to about 2% by weight.
Suitable polymers are high molecular weight materials (mass- average molecular weight determined, for instance, by light scattering, being generally from about 2,000 to about 5,000,000, preferably from about 5,000 to about 3,000,000 more preferably from 100,000 to about 1,000,000).
Representative classes of polymers include cationic and nonionic polysaccharides; cationic and nonionic homopolymers and copolymers derived from acrylic and/or methacrylic acid; cationic and nonionic cellulose resins; cationic copolymers of dimethyldiallylammonium chloride and acrylamide and or acrylic acid; cationic homopolymers of dimethyldiallylammonium chloride; cationic polyalkylene and ethoxypolyalkylene imines; quaternized silicones, and mixtures thereof.
By way of exemplification, cationic polymers suitable for use herein include cationic guar gums such as hydroxypropyl trimethyl ammonium guar gum (d.s. of from 0.11 to 0.22) available commercially under the trade names Jaguar C-14-S(RTM) and Jaguar C-17(RTM) and also Jaguar C-16(RTM), which contains hydroxypropyl substituents (d.s. of from 0.8- 1.1) in addition to the above-specified cationic groups, and quaternized cellulose ethers available commercially under the trade names Ucare Polymer JR-30M, JR-400 and Celquat. Other suitable cationic polymers are homopolymers of dimethyldiallylammonium chloride available commercially under the trade name Merquat 100, copolymers of dimethyl aminoethylmethacrylate and acrylamide, copolymers of dimethyldiallylammonium chloride and acrylamide, available commercially under the trade names Merquat 550 and Merquat S, acrylic acid/dimethyldiallylammonium chloride/acrylamide copolymers available under the trade name Merquat 3300, quaternized vinyl pyrrolidone aery late or methacrylate copolymers of amino alcohol available commercially under the trade name Gafquat, for example Polyquatemium 11 , 23 and 28 (quaternized copolymers of vinyl pyrrolidone and dimethyl aminoethylmethacrylate - Gafquat 755N and HS-100), vinyl pyrrolidone/vinyl imidazolium methochloride copolymers available under the trade names Luviquat HM552, Polyquatemium 2, and polyalkyleneimines such as polyethylenimine and ethoxylated polyethylenimine. Highly preferred from the viewpoint of providing a "draggy" soap-like feel are the quaternized vinyl pyrrolidone acrylate and methacrylate copolymers In preferred embodiments the weight ratio of water-insoluble metal salt: polymeric skin conditioning agent is in the range from about 50:1 to about 1 :10.
Mild surfactants suitable for inclusion in compositions according to the present invention can be selected from anionic, nonionic, amphoteric and zwitterionic surfactants and mixtures thereof. The total level of surfactant is preferably from about 5% to about 60%, more preferably from about 8% to about 40%, and especially from about 10% to about 35% by weight. The compositions preferably comprise a mixture of anionic with zwitterionic and/or amphoteric surfactants. The level of the individual anionic, zwitterionic and amphoteric surfactant components, where present, is in the range from about 1 % to about 15%, and especially from about 2% to about 13% by weight of the composition, while the level of nonionic surfactant, where present, is in the range from about 0.1 % to about 20% by weight, preferably from about 2% to about 16%, more preferably from about 3% to about 12% by weight. The total level of anionic, amphoteric, and zwitterionic surfactant components, is preferably from about 5% to about 50%, more preferably from about 8% to about 35% and especially from about 10% to about 30% by weight of composition. The weight ratio of anionic surfactant: zwitterionic and/or amphoteric surfactant is in the range from about 1:2 to about 6:1. Other suitable compositions within the scope of the invention comprise mixtures of anionic, zwitterionic and/or amphoteric surfactants with one or more nonionic surfactants. Preferred for use herein are soluble or dispersible nonionic surfactants selected from ethoxylated animal and vegetable oils and fats and mixtures thereof, sometimes referred to herein as "oil- derived" nonionic surfactants.
Anionic surfactants suitable for inclusion in the compositions of the invention can generally be described as mild synthetic detergent surfactants and include ethoxylated alkyl sulfates, alkyl glyceryl ether sulfonates, methyl acyl taurates, fatty acyl glycinates, N-acyl glutamates, acyl isethionates, alkyl sulfosuccinates, alpha-sulfonated fatty acids, their salts and/or their esters, alkyl ethoxy carboxylates, alkyl phosphate esters, ethoxylated alkyl phosphate esters, acyl sarcosinates and fatty acid/protein condensates, and mixtures thereof. Alkyl and/or acyl chain lengths for these surfactants are Cg-C22» preferably C10-C18 more preferably
C12-C14-
Preferred for use herein from the viewpoint of optimum mildness and lathering characteristics are the salts of sulfuric acid esters of the reaction product of 1 mole of a higher fatty alcohol and from about 1 to about 12 moles of ethylene oxide, with sodium and magnesium being the preferred counterions. Particularly preferred are the alkyl sulfates containing from about 2 to 6, preferably 2 to 4 moles of ethylene oxide, such as sodium laureth-2 sulfate, sodium laureth-3 sulfate and magnesium sodium laureth-3.6 sulfate. In preferred embodiments, the anionic surfactant contains at least about 50%, especially at least about 75% by weight of ethoxylated alkyl sulfate. The compositions for use herein suitably also contain an amphoteric surfactant. Amphoteric surfactants suitable for use in the compositions of the invention include:
(a) imidazolinium surfactants of formula (I)
Figure imgf000009_0001
wherein Ri is C7-C22 alkyl or alkenyl, R2 is hydrogen or CH2Z, each Z is independently CO2M or CH2CO2M, and M is H, alkali metal, alkaline earth metal, ammonium or alkanolammonium; and/or ammonium derivatives of formula (ID
Figure imgf000009_0002
R2
wherein Ri, R2 and Z are as defined above;
(b) aminoalkanoates of formula (III)
RlNH(CH2)nC02M
iminodialkanoates of formula (IV)
RlN[(CH2)mC02M]2
and iminopolyalkanoates of formula (V)
Rl.[N(CH2)p]qN[CH2Cθ2M]2 CH2CO2M
wherein n, m, p, and q are numbers from 1 to 4, and Rj and
M are independently selected from the groups specified above; and
(c) mixtures thereof.
Suitable amphoteric surfactants of type (a) are marketed under the trade name Miranol and Empigen and are understood to comprise a complex mixture of species. Traditionally, the Miranols have been described as having the general formula I, although the CTFA Cosmetic Ingredient Dictionary, 3rd Edition indicates the non-cyclic structure II while the 4th Edition indicates yet another structural isomer in which R2 is
O-linked rather than N-linked. In practice, a complex mixture of cyclic and non-cyclic species is likely to exist and both defmitions are given here for sake of completeness. Preferred for use herein, however, are the non- cyclic species.
Examples of suitable amphoteric surfactants of type (a) include compounds of formula I and/or II in which R\ is CgHπ (especially iso- capryl), C9H19 and C11H23 alkyl. Especially preferred are the compounds in which Ri is C9H19, Z is CO2M and R2 is H; the compounds in which Ri is C11H23, Z is CO2M and R2 is CH2CO2M; and the compounds in which R\ is C11H23, Z is CO2M and R2 is H.
In CTFA nomenclature, materials suitable for use in the present invention include cocoamphocarboxypropionate, cocoamphocarboxy prop ionic acid, and especially cocoamphoacetate and cocoamphodiacetate (otherwise referred to as cocoamphocarboxyglycinate). Specific commercial products include those sold under the trade names of Ampholak 7TX (sodium carboxy methyl tallow polypropyl amine), Empigen CDL60 and CDR 60 (Albright & Wilson), Miranol H2M Cone. Miranol C2M Cone. N.P., Miranol C2M Cone. O.P., Miranol C2M SF, Miranol CM Special (Rhόne-Poulenc); Alkateric 2CIB (Alkaril Chemicals); Amphoterge W-2 (Lonza, Inc.); Monateric CDX-38, Monateric CSH-32 (Mona Industries); Rewoteric AM-2C (Rewo Chemical Group); and Schercotic MS-2 (Scher Chemicals).
It will be understood that a number of commercially-available amphoteric surfactants of this type are manufactured and sold in the form of electroneutral complexes with, for example, hydroxide counterions or with anionic sulfate or sulfonate surfactants, especially those of the sulfated Cg-Ci8 alcohol, Cg-Ci8 ethoxylated alcohol or C8-Cχ8 acyl glyceride types. Preferred from the viewpoint of mildness and product stability, however, are compositions which are essentially free of (non- ethoxylated) sulfated alcohol surfactants. Note also that the concentrations and weight ratios of the amphoteric surfactants are based herein on the uncomplexed forms of the surfactants, any anionic surfactant counterions being considered as part of the overall anionic surfactant component content.
Examples of preferred amphoteric surfactants of type (b) include N-alkyl polytrimethylene poly-, carboxymethylamines sold under the trade names Ampholak X07 and Ampholak 7CX by Berol Nobel and also salts, especially the triethanolammonium salts and salts of N-lauryl-beta-amino propionic acid and N-lauryl-imino-dipropionic acid. Such materials are sold under the trade name Deriphat by Henkel and Mirataine by Rhόne- Poulenc.
The compositions herein can also contain from about 0.1 % to about 20%, more preferably from about 0.1 % to about 10% , and especially from about 1 % to about 8% of a zwitterionic surfactant, especially an alkyl betaine or amidobetaine surfactant.
Betaine surfactants suitable for inclusion in the composition of the invention include alkyl betaines of the formula R5R-6R7N+(CH2)nC02M(VIII) and amido betaines of the formula (IX) i 6
R5C0N ( CH2 ) mN ( CH2 ) nC02M
R7
wherein R5 is C12-C22 alkyl or alkenyl, R$ and R7 are independently C1-C3 alkyl, M is H, alkali metal, alkaline earth metal, ammonium or alkanolammonium, and n, m are each numbers from 1 to 4. Preferred betaines include cocoamidopropyldimethylcarboxy methyl betaine, laurylamidopropyldimethylcarboxy methyl betaine and Tego betaine.
The compositions of the invention preferably also contain from about 0.1 % to about 20%, preferably from about 1 % to about 15%, and more preferably from about 2% to about 10% by weight of an oil derived nonionic surfactant or mixture of oil derived nonionic surfactants. Oil derived nonionic surfactants are valuable in compositions according to the invention for the provision of skin feel benefits both in use and after use. Suitable oil derived nonionic surfactants for use herein include water soluble vegetable and animal-derived emollients such as triglycerides with a polyethyleneglycol chain inserted; ethoxylated mono and di-glycerides, polyethoxylated lanolins and ethoxylated butter derivatives. One preferred class of oil-derived nonionic surfactants for use herein have the general formula (VI)
RCOCH2CH (OH) CH2 (OCH2CH2 ) nOH
wherein n is from about 5 to about 200, preferably from about 20 to about 100, more preferably from about 30 to about 85, and wherein R comprises an aliphatic radical having on average from about 5 to 20 carbon atoms, preferably from about 9 to 18 carbon atoms.
Suitable ethoxylated oils and fats of this class include polyethyleneglycol derivatives of glyceryl cocoate, glyceryl caproate, glyceryl caprylate, glyceryl tallowate, glyceryl palmate, glyceryl stearate, glyceryl laurate, glyceryl oleate, glyceryl ricinoleate, and glyceryl fatty esters derived from triglycerides, such as palm oil, almond oil, and corn oil, preferably glyceryl tallowate and glyceryl cocoate.
Suitable oil derived nonionic surfactants of this class are available from Croda Inc. (New York, USA) under their Crovol line of materials such as Crovol EP40 (PEG 20 evening primrose glyceride), Crovol EP 70 (PEG 60 evening primrose glyceride) Crovol A-40 (PEG 20 almond glyceride), Crovol A-70 (PEG 60 almond glyceride), Crovol M-40 (PEG 20 maize glyceride), Crovol M-70 (PEG 60 maize glyceride), Crovol PK- 40 (PEG 12 palm kernel glyceride), and Crovol PK-70 (PEG 45 palm kernel glyceride) and under their Solan range of materials such as Solan E, E50 and X polyethoxylated lanolins and Aqualose L-20 (PEG 24 lanolin alcohol) available from Westbrook Lanolin. Further suitable surfactants of this class are commercially available from Sherex Chemical Co. (Dublin, Ohio, USA) under their Varonic LI line of surfactants. These include, for example, Varonic LI 48 (polyethylene glycol (n=80) glyceryl tallowate, alternatively referred to as PEG 80 glyceryl tallowate), Varonic LI 2 (PEG 28 glyceryl tallowate), Varonic LI 420 (PEG 200 glyceryl tallowate), and Varonic LI 63 and 67 (PEG 30 and PEG 80 glyceryl cocoates). Other oil-derived emollients suitable for use are PEG derivatives of com, avocado, and babassu oil, as well as Softigen 767 (PEG(6) caprylic/capric glycerides).
Also suitable for use herein are nonionic surfactants derived from composite vegetable fats extracted from the fruit of the Shea Tree (Butyrospermum Karkii Kotschy) and derivatives thereof. This vegetable fat, known as Shea Butter is widely used in Central Africa for a variety of means such as soap making and as a barrier cream, it is marketed by Sederma (78610 Le Perray En Yvelines, France). Particularly suitable are ethoxylated derivatives of Shea butter available from Karlshamn Chemical Co. (Columbos, Ohio, USA) under their Lipex range of chemicals, such as Lipex 102 E-75 (ethoxylated mono, di-glycerides of Shea butter). Similarly, ethoxylated derivatives of Mango, Cocoa and Illipe butter may be used in compositions according to the invention. Although these are classified as ethoxylated nonionic surfactants it is understood that a certain proportion may remain as non-ethoxylated vegetable oil or fat. Other suitable oil-derived nonionic surfactants include ethoxylated derivatives of almond oil, peanut oil, rice bran oil, wheat germ oil, linseed oil, jojoba oil, oil of apricot pits, walnuts, palm nuts, pistachio nuts, sesame seeds, rapeseed, cade oil, com oil, peach pit oil, poppyseed oil, pine oil, castor oil, soybean oil, avocado oil, safflower oil, coconut oil, hazlenut oil, olive oil, grapeseed oil, and sunflower seed oil.
Oil derived nonionic surfactants highly preferred for use herein from the viewpoint of optimum mildness and skin feel characteristics are PEG 60 evening primrose triglycerides; PEG 55 lanolin polyethoxylated derivatives and ethoxylated derivatives of Shea butter.
In addition to the above oil derived nonionic surfactants, the compositions of the invention can also comprise an auxiliary nonionic surfactant at levels from about 0.1 % to about 20%, more preferably from about 0.1 % to about 10%, and especially from about 1 % to about 8% by weight. Surfactants of this class include C12-C14 fatty acid mono-and diethanolamides, sucrose polyester surfactants and polyhydroxy fatty acid amide surfactants having the general formula (VII).
o Rq
II
R8 —C- N— z2
The preferred polyhydroxy fatty acid amide surfactants are those in which R9 is Cι_4 alkyl, preferably methyl, and R8 is C7-C19 alkyl or alkenyl, more preferably straight-chain C9-C17 alkyl or alkenyl, or mixture thereof; and Z2 is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative (preferably ethoxylated or propoxylated) thereof. Z2 preferably will be derived from a reducing sugar in a reductive amination reaction; more preferably Z2 is a glycityl.
Suitable reducing sugars include glucose, fructose, maltose, lactose, galactose, mannose, and xylose. As raw materials, high dextrose com syrup, high fructose com syrup, and high maltose com syrup can be utilized as well as the individual sugars listed above. These com syrups may yield a mix of sugar components for Z2- It should be understood that it is by no means intended to exclude other suitable raw materials. Z2 preferably will be selected from the group consisting of -CH2(CHOH)n- CH2θH,-CH(CH2θH)-(CHOH)n.ι-CH2θH, -CH2- (CHOH)2(CHOR')(CHOH)-CH2θH, where n is an integer from 3 to 5, inclusive, and R' is H or a cyclic or aliphatic monosaccharide, and alkoxylated derivatives thereof. Most preferred are glycityls wherein n is 4, particularly -CH2-(CHOH)4-CH2θH.
The most preferred polyhydroxy fatty acid amide has the formula Rg(CO)N(CH3)CH2(CHOH)4CH2θH wherein R% is a C11-C17 straight chain alkyl or alkenyl group.
The compositions of the invention may also contain from about 0.1 % to about 8%, preferably from about 0.5% to about 6%, and especially from about 1.5% to about 5% by weight of saturated acyl fatty acids having a weight average chain length of from 10 to 18, preferably from 12 to 16 carbon atoms. Highly preferred is myristic acid.
The compositions of the invention may also include an insoluble perfume or cosmetic oil or wax or a mixture thereof at a level up to about 10% , preferably up to about 3% by weight wherein the oil or wax is insoluble in the sense of being insoluble in the product matrix at a temperature of 25 °C. Addition of such oils or waxes can provide emolliency, mildness and rinsibility characteristics to personal cleansing compositions according to the invention. It is a feature of the invention, however, that compositions having excellent emolliency and mildness together with desirable physical attributes (clarity etc.) can be delivered which are essentially oil-free, ie which contain less than about 1 % , preferably less than 0.5% by weight of an added oil phase. Physically, preferred compositions of this type take the form of an optically-clear solution or microemulsion. In compositions including an additional perf ime or cosmetic oil or wax, preferably the weight ratio of oil-derived nonionic surfactant to added oil is at least about 1 :2, more especially at least about 3:1. Suitable insoluble cosmetic oils and waxes for use herein can be selected from water-insoluble silicones inclusive of non-volatile polyalkyl and polyaryl siloxane gums and fluids, volatile cyclic and linear polyalkylsiloxanes, polyalkoxylated silicones, amino and quaternary ammonium modified silicones, rigid cross-linked and reinforced silicones and mixtures thereof, -C24 esters of C8-C30 fatty acids such as isopropyl myristate, myristyl myristate and cetyl ricinoleate, C -C30 esters of benzoic acid, beeswax, saturated and unsaturated fatty alcohols such as behenyl alcohol, hydrocarbons such as mineral oils, petrolatum squalane and squalene, polybutene, fatty sorbitan esters (see US-A- 3988255, Seiden, issued October 26th 1976), lanolin and oil-like lanolin derivatives, animal and vegetable triglycerides such as almond oil, peanut oil, wheat germ oil, rice bran oil, linseed oil, jojoba oil, oil of apricot pits, walnuts, palm nuts, pistachio nuts, sesame seeds, rapeseed, cade oil, com oil, peach pit oil, poppyseed oil, pine oil, castor oil, soybean oil, avocado oil, safflower oil, coconut oil, hazlenut oil, olive oil, grapeseed oil, and sunflower seed oil, and C1-C24 esters of dimer and trimer acids such as diisopropyl dimerate, diisostearylmalate, diisostearyldimerate and triisostearyltrimerate.
The viscosity of the final composition (Brookfield RVT DCP, 1 rpm with Cone CP41 or CP52, 25 °C, neat) is preferably at least about 500 cps, more preferably from about 1 ,000 to about 50,000 cps, especially from about 5,000 to about 30,000 cps, the viscosity being controlled using conventional hydrophilic gelling agents and thickeners.
The compositions of the invention thus can also contain a hydrophilic gelling agent at a level preferably from about 0.01 % to about 10%, more preferably from about 0.02% to about 2%, and especially from about 0.02% to about 0.5%. The gelling agent preferably has a viscosity (1 % aqueous solution, 20°C, Brookfield RVT) of at least about 4000 mPa.s, more preferably a least about 10,000 mPa.s and especially at least 50,000 mPa.s.
Suitably hydrophilic gelling agents can generally be described as water-soluble or colloidally water-soluble polymers, and include cellulose ethers (e.g. hydroxyethyl cellulose, methyl cellulose, hydroxypropylmethyl cellulose), polyvinylpyrrolidone, polyvinylalcohol, guar gum, hydroxpropyl guar gum and xanthan gum.
Preferred hydrophilic gelling agents herein, however, are acrylic acid/ethyl acrylate copolymers and the carboxyvinyl polymers sold by the B.F. Goodrich Company under the trade mark of Carbopol resins. These resins consist essentially of a colloidally water-soluble polyalkenyl polyether crosslinked polymer of acrylic acid crosslinked with from 0.75% to 2.00% of a crosslinked agent such as for example polyallyl sucrose or polyallyl pentaerythritol. Examples include Carbopol 934, Carbopol 940, Carbopol 950, Carbopol 980, Carbopol 951 and Carbopol 981. Carbopol 934 is a water-soluble polymer of acrylic acid crosslinked with about 1 % of a polyallyl ether of sucrose having an average of about 5.8 allyl groups for each sucrose molecule. A most preferred polymer is Carbopol 951. Also suitably for use herein are hydrophobically-modified cross-linked polymers of acrylic acid having amphipathic properties available under the Trade Name Carbopol 1382, Carbopol 1342 and Pemulen TR-1 (CFTA Designation: Acrylates/10-30 Alkyl Acrylate Crosspolymer). A combination of the polyalkenyl polyether cross-linked acrylic acid polymer and hydrophobically modified cross-linked acrylic acid polymer is also suitable for use herein. The gelling agents herein are particularly valuable for providing excellent stability characteristics over both normal and elevated temperatures.
Neutralizing agents suitable for use in neutralizing acidic group contining hydrophilic gelling agents herein include sodium hydroxide, potasssium hydroxide, ammonium hydroxide, monoethanoiamine, diethanolamine and triethanolamine.
The cleansing compositions can optionally include other hair or skin moisturizers which are soluble in the cleansing composition matrix. The preferred level of such moisturizers is from about 0.5% to about 20% by weight. In preferred embodiments, the moisturizer is selected from:
1. water-soluble liquid polyols;
2. essential amino acid compounds found naturally occurring in the stratum corneum of the skin; and 3. water-soluble nonpolyol nonocclusives and mixtures thereof.
Some examples of more preferred nonocclusive moisturizers are polybutene, squalane, glycerine, polyethylene glycol, propylene glycol, sorbitol, polyethylene glycol and propylene glycol ethers of methyl glucose (e.g. ethyl glucam E-20 and propylglucan P-10), polyethylene glycol and propylene glycol ethers of lanolin alcohol (e.g. Solulan-75), sodium pyrrolidone carboxylic acid, lactic acid, L-proline, guanidine, pyrrolidone, hydrolyzed protein and other collagen-derived proteins, aloe vera gel and acetamide MEA and mixtures thereof. Of the above, glycerine is highly preferred.
A number of additional optional materials can be added to the cleansing compositions each at a level of from about 0.1 % to about 2% by weight. Such materials include proteins and polypeptides and derivatives thereof; water-soluble or solubilizable preservatives such as DMDM Hydantoin, Germall 115, methyl, ethyl, propyl and butyl esters of hydroxybenzoic acid, EDTA, Euxyl (RTM) K400, natural preservatives such as benzyl alcohol, potassium sorbate and bisabalol; sodium benzoate and 2-phenoxyethanol; other moisturizing agents such as hyaluronic acid, chitin , and starch-grafted sodium polyacrylates such as Sanwet (RTM) IM-1000, IM-1500 and IM-2500 available from Celanese Superabsorbent Materials, Portsmith, VA, USA and described in US-A-4,076,663; solvents such as hexylene glycol and propylene glycol; anti-bacterial agents such as Oxeco (phenoxy isopropanol); low temperature phase modifiers such as ammonium ion sources (e.g. NH4 Cl); viscosity control agents such as magnesium sulfate and other electrolytes; colouring agents; pearlescers and opacifiers such as ethylene glycol distearate, TiC*2 and
Tiθ2-coated mica; perfumes and perfume solubilizers; and zeolites such as Valfour BV400 and derivatives thereof and Ca2+/Mg2+ sequestrants such as polycarboxylates, amino polycarboxylates, polyphosphonates, amino polyphosphonates etc. Water is also present at a level preferably of from about 45% to about 94% preferably at least about 60% by weight of the compositions herein. The pH of the compositions is preferably from about 4 to about 10, more preferably from about 6 to about 9.
The invention is illustrated by the following non-limiting examples.
In the examples, all concentrations are on a 100% active basis and the abbreviations have the following designation:
Amphoteric Cocoamphodiacetate
Anionic 1 Sodium laureth-3 sulfate
Anionic 2 Sodium lauroyl sarcosinate
Solan Solan (RTM) E (PEG 55 lanolin)
Crovol Crovol (RTM) EP 70 (PEG 60 evening primrose triglycerides)
GA Polyhydroxy fatty acid amide of formula VII in which R is Cι ι-Ci7 alkyl, R9 is methyl, and Z2 is
CH2(CHOH)4CH2θH
Betaine Cocoamidopropyl betaine
Polymer 1 Polymer JR-400 - hydroxyethylcellulose reacted with epichlorohydrin and quaternized with trimethylamine, m.wt. 4 x 106
Polymer 2 Gafquat 755N
Preservative Phenoxyethanol/sodium benzoate/EDTA (4:2: 1)
Pearlescer Ethyleneglycoldistearate/emulsifier mixture Oil Soyabean Oil
Softigen 767 PEG(6) caprylic/capric glycerides
Examples I to VI
The following are personal cleansing compositions in the form of shower gel or bath foam products and which are representative of the present invention:
I II III IV V VI
Amphoteric 3.0 3.0 - 5.0 - 4.0
Anionic 1 6.0 6.0 13.0 10.0 6.0 4.0
Anionic 2 1.0 2.0 2.0 2.0 1.0
GA 3.0 - - 3.0 3.0 2.0
Betaine - - 4.0 - 3.0 -
Oil - 4.0 4.0 6.0 4.0
Softigen 767 - 3.0 - 2.0 2.0
Solan - 3.0 - 1.0 - 2.0
Crovol - - 1.0 - - 3.0
Polymer 1 0.8 1.0 - 1.0 1.0 -
Polymer 2 - - 0.5 - - 0.2
Pearlescer 1.0 1.0 3.0 3.0 1.0 1.0
Preservative 1.0 1.0 1.0 1.0 1.0 1.0
Perfume 1.0 1.0 1.0 1.0 1.0 1.0 Glycerine 3.0 3.0 - 3.0
Carbomer 0.2 0.3 0.4 0.3 0.5 0.2
1342
Zinc Stearate 0.8 0.5 0.8 4.0 2.5 1.0
Water to 100
Compositions I to VI are prepared by forming a surfactant phase A at about 65 °C containing a portion of the water, the anionic, amphoteric and oil-derived nonionic surfactants and the remaining water-soluble, oil- insoluble ingredients. In compositions which comprise water-insoluble ingredients an oil phase B is formed from these oil-soluble ingredients which is then admixed with A at about 65 °C and cooled to ambient temperature. Finally the remaining water, preservative and perfume are added.
The products provide excellent in-use and efficacy benefits including mildness, soap-like skin feel, skin conditioning, skin moisturising, stability, cleansing, lathering and rinsibility.

Claims

WHAT IS CLAIMED IS :
1. A liquid personal cleansing composition comprising:
a) from about 5% to about 60% by weight of surfactant selected from anionic, nonionic, zwitterionic and amphoteric surfactants and mixtures therefor;
b) from about 0.1 % to about 5% by weight of a water- insoluble salt of a C14-C22 fatty acid;
c) optionally from about 0.01 % to about 5 % by weight of a cationic or nonionic polymeric skin conditioning agent; and
d) water.
2. A composition according to Claim 1 wherein the water-insoluble salt is selected from zinc, magnesium, calcium, lithium and aluminium salts of C14-C22 fatty acids and mixtures thereof.
3. A composition according to Claim 2 wherein the water-insoluble salt is zinc stearate.
4. A composition according to any of Claims 1 to 3 comprising from about 0.5% to about 2% by weight of the water-insoluble salt of a C14-C22 fatty acid.
5. A composition according to any of Claims 1 to 4 wherein the composition has a viscosity (Brookfield RVT DCP, 1 rpm with Cone CP41 or CP52, 25 °C, neat) in the range from 1,000 to 50,000 cps.
6. A composition according to any of Claims 1 to 5 wherein the polymeric skin conditioning agent has a mass average molecular weight in the range from about 2000 to about 5,000,000 preferably between about 5000 to about 3,000,000.
7. A composition according to any of Claims 1 to 6 wherein the polymeric skin conditioning agent is selected from cationic and nonionic poly sacchar ides; cationic and nonionic homopolymers and copolymers derived form acrylic and/or methacrylic acid; cationic and nonionic cellulose resins; cationic copolymers of dimethyldiallylammonium chloride and acrylic acid; cationic homopolymers of dimethyldiallylammonium chloride; cationic polyalkylene and ethoxypolyalkylene i mines; quaternized silicones, and mixtures thereof.
8. A composition according to any of Claims 1 to 7 wherein the weight ratio of water-insoluble fatty acid salt: polymeric skin conditioning agent is in the range from about 50: 1 to about 1 : 10.
9. A composition according to any of Claims 1 to 8 comprising a mixture of anionic with zwitterionic and/or amphoteric surfactants and wherein the level of the individual anionic, zwitterionic and amphoteric surfactant components is in the range from about 1 % to 15% , preferably from about 2% to about 13% by weight.
10. A composition according to any of Claims 1 to 9 comprising from about 0.1 % to about 20% by weight of nonionic surfactant selected from ethoxylated oils or fats having the formula [V]
o
II
RCOCH2CH(OH)CH2(0CH2CH2)nOH
wherein n is from about 5 to 200, preferably from about 20 to about 100, more preferably from about 30 to about 85, and wherein R comprises an aliphatic radical having an average from about 5 to 20 carbon atoms, preferably from about 9 to 20 atoms, more preferably from about 11 to 18 carbon atoms, most preferably from about 12 to 16 carbon atoms.
11. A composition according to any of Claims 1 to 10 wherein the anionic surfactant is selected from ethoxylated alkyl sulfates, alkyl glyceryl ether sulfonates, methyl acyl taurates, fatty acyl glycinates, alkyl ethoxy carboxylates, N-acyl glutamates, acyl isethionates, alkyl sulfosuccinates, alpha-sulfonated fatty acids, their salts and/or their esters, alkyl phosphate esters, ethoxylated alkyl phosphate esters, acyl sarcosinates and fatty acid/protein condensates, and mixtures thereof.
12. A composition according to any of Claims 1 to 11 wherein the anionic surfactant comprises an ethoxylated Cg-C22 alkyl sulfate.
13. A composition according to any of the Claims 1 to 12 wherein the amphoteric surfactant is selected from:
(a) imidazolinium derivatives of formula [I]
Figure imgf000026_0001
wherein R\ is C7-C22 alkyl or alkenyl, R2 is hydrogen of CH2Z, each Z is independently CO2 or CH2 CO2M, and M is H, alkali metal, alkaline earth metal, ammonium or alkanolammonium; and/or ammonium derivatives of formula [II]
Figure imgf000026_0002
R2
wherein Ri, R2 and Z are as defined above:
(b) aminoalkanoates of formula [III]
RlNH(CH2)nCθ2M
iminodialkanoates of formula [TV] RlN[(CH2)mC02M]2
and iminopolyalkanoates of formula (V)
Rι [N(CH2)p]q - N [CH2Cθ2M]2
I CH2C02M
wherein n, m, p, and q are numbers from 1 to 4, and R\ and M are independently selected from the groups specified above; and
(c) mixtures thereof.
14. A composition according to Claim 13 wherein the amphoteric is selected from imidazolinium derivatives of formula I and/or ammonium derivatives of formula II.
15. A composition according to any of the Claims 1 to 14 wherein the weight ratio of anionic surfactant: zwitterionic and/or amphoteric surfactant is in the range of from about 1 :2 to about 6: 1.
16. A composition according to any of the Claims 1 to 15 wherein the anionic, zwitterionic and amphoteric surfactants together comprise from about 8% to about 35% , preferably from about 10% to about 30% by weight of the composition.
17. A composition according to any of Claims 1 to 16 which additionally comprises from about 0.1 % to about 20% by weight of an auxiliary nonionic surfactant selected from C12-C14 fatty acid mono-and diethanolamides and polyhydroxy fatty acid amide surfactants.
18. A composition according to any of Claims 1 to 17 additionally comprising up to about 20% by weight of perfume or cosmetic oil.
19. A composition according to any of Claims 1 to 18 additionally comprising moisturiser selected from glycerin, polyethylene glycol, propylene glycol, sorbitol, polyethylene glycol and polypropylene glycol ethers of methyl glycose, sodium pyrrolidone carboxylic acid, L-proline and mixtures thereof.
PCT/US1995/000607 1993-11-11 1995-01-13 Cleansing compositions WO1996021425A1 (en)

Priority Applications (4)

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GB9323283A GB2283754B (en) 1993-11-11 1993-11-11 Cleaning compositions
PCT/US1995/000607 WO1996021425A1 (en) 1993-11-11 1995-01-13 Cleansing compositions
JP8521624A JPH10512254A (en) 1993-11-11 1995-01-13 Cleansing composition
EP95908533A EP0794766A4 (en) 1993-11-11 1995-01-13 Cleansing compositions

Applications Claiming Priority (2)

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PCT/US1995/000607 WO1996021425A1 (en) 1993-11-11 1995-01-13 Cleansing compositions

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WO2018000063A1 (en) * 2016-06-30 2018-01-04 L'oreal Non-pressurized foaming cosmetic products and foaming cosmetic compositions
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GB9323283D0 (en) 1994-01-05
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EP0794766A4 (en) 2000-05-10
JPH10512254A (en) 1998-11-24
GB2283754B (en) 1998-01-28

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