US20030108505A1 - Use of xanthan gum as a hair fixative - Google Patents

Use of xanthan gum as a hair fixative Download PDF

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Publication number
US20030108505A1
US20030108505A1 US09/932,435 US93243501A US2003108505A1 US 20030108505 A1 US20030108505 A1 US 20030108505A1 US 93243501 A US93243501 A US 93243501A US 2003108505 A1 US2003108505 A1 US 2003108505A1
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Prior art keywords
composition
xanthan gum
copolymer
acrylates
hair
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US09/932,435
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Hongjie Cao
Gary Martino
Paul Richardson
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Akzo Nobel NV
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National Starch and Chemical Investment Holding Corp
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Priority to US09/932,435 priority Critical patent/US20030108505A1/en
Assigned to NATIONAL STARCH AND CHEMICAL INVESTMENT HOLDING CORPORATION reassignment NATIONAL STARCH AND CHEMICAL INVESTMENT HOLDING CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: RICHARDSON, PAUL H., MARTINO, GARY T., CAO, HONGJIE
Priority to US10/198,469 priority patent/US9072683B2/en
Priority to DE10237257A priority patent/DE10237257A1/en
Priority to GB0218928A priority patent/GB2380938B/en
Priority to JP2002236931A priority patent/JP4920854B2/en
Priority to MXPA02007911A priority patent/MXPA02007911A/en
Priority to FR0210368A priority patent/FR2828645B1/en
Priority to CNB021437351A priority patent/CN100482205C/en
Priority to BR0203284-8A priority patent/BR0203284A/en
Publication of US20030108505A1 publication Critical patent/US20030108505A1/en
Priority to JP2008121664A priority patent/JP5511151B2/en
Assigned to AKZO NOBEL N.V. reassignment AKZO NOBEL N.V. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: NATIONAL STARCH AND CHEMICAL INVESTMENT HOLDING CORPORATION
Abandoned legal-status Critical Current

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    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/06Preparations for styling the hair, e.g. by temporary shaping or colouring

Definitions

  • the present invention relates to the use of xanthan gum, particularly heat treated xanthan gum, as a fixative in hair cosmetic compositions and hair fixative compositions comprising xanthan gum.
  • Xanthan gum is a polysaccharide gum derived from the bacterium Xanthomonas and is well known in the art. It is composed of a main chain comprising ⁇ -(1,4) D-glucose units. Trisaccharide side chains on alternating anhydroglucose units are composed of a glucuronic acid residue between two mannose units. At most of the terminal mannose units is a pyruvate moiety and the non-terminal mannose carries an acetyl group. It has pseudoplastic or shear-thinning behavior characterized by a decrease in apparent viscosity in response to an increase in shear rate.
  • Xanthan gum is typically used in many industrial applications as a rheology modifier; thickening, viscosifying and gelling when combined with other polymers. It has also been used to impart stability to emulsions and prevent the settling out of solids. Its limited ability to disperse in either hot or cold water allows xanthan gum to be formulated into a broad variety of applications including pharmaceuticals, household products, foods, and personal care products.
  • Xanthan gum with an apparent average molecular weight of greater than 16,000,000 has been used to stabilize and improve the feel of emulsified cosmetics such as toilet water, creams and cleansing gels (JP Application No. 10-140503).
  • Xanthan gum which has been heat-treated is also known in the art.
  • EP 321 216 enhances the viscosity profile of xanthan gum by thermally treating it in the dry state (15% moisture or less).
  • Heat treatment of xanthan gum is also known in JP Application No. 8-193055 which heat treats xanthan gum in the powdered form.
  • xanthan gum particularly heat treated xanthan gum, is a suitable fixative for hair cosmetic compositions.
  • the present invention is directed to the use of xanthan gum, particularly heat treated xanthan gum, as a fixative in hair cosmetic compositions.
  • Xanthan gum is advantageous in that it may be used with other hair fixatives and provides rheology modifying and other properties including excellent stiffness, gloss, dry comb, wet comb, non-flake, anti-static, feel and high humidity curl retention.
  • the present invention is directed to the use of xanthan gum, particularly heat treated xanthan gum, as a fixative in hair cosmetic compositions.
  • the xanthan gum may be used in a purified form or may be heat treated. Heat treatment of xanthan gum is typically done at low moisture, particularly less than about 25%, more particularly less than about 8%, most particularly less than about 1%, at a temperature of at least about 60° C., more particularly at least 100° C., and most particularly at least about 105° C. for a period of time of about 30 minutes, particularly at least one hour, more particularly at least 2.5 hours.
  • the moisture content, pH, temperature and time of heat treatment may be adjusted by one skilled in the art to achieve the viscosity, dispersibility, gel texture, solution clarity, and other properties desired. It will further be dependent upon the starting material used (grade, viscosity, molecular weight, and particle size). Typically, low moisture is used to improve the impact of heat-treatment. However, at any given moisture, increasing the temperature or time generally increases viscosity to a maximum and further heating decreases the viscosity of the xanthan gum at the concentrations used in this invention. Acidic pH are typically more suitable; a pH of 2-4 is most suitable.
  • Heat treatment of xanthan gum may be accomplished by a variety of methods known in the art including without limitation oven, fluidized bed, infrared and microwave heat treatments.
  • the particle size of the resultant heat-treated xanthan gum may be adjusted using methods known in the art such as milling.
  • the xanthan gum may further be modified either before or after heat treatment.
  • the xanthan gum may be converted by oxidation, enzyme conversion, acid hydrolysis, heat and/or acid dextrinization, or shear.
  • the xanthan gum may also be chemically, enzymatically or physically modified. Suitable chemical derivatives include esters, such as the acetate, and half esters, such as the succinate, octenyl succinate and tetradecenyl succinate; phosphate derivatives; ethers such as hydroxyalkyl ethers and cationic ethers; or any other derivatives or combinations thereof. Modification may also be by chemical crosslinking.
  • Crosslinking agents suitable for use herein include phosphorus oxychloride, epichlorohydrin, sodium trimetaphosphate and adipic-acetic mixed acid anyhrides. Such processes are also known in the art. Typically, the xanthan gum will not be modified other than by crosslinking or heat treatment.
  • the xanthan gum may also be purified by any method known in the art to remove off flavors and colors that are native to the xanthan gum or are created during the modification or heat treatment processes as long as the heat treatment is not substantially impacted.
  • the resultant heat-treated xanthan gum has improved dispersibility, such that under given conditions of temperature and agitation, the time to fully disperse the resultant gum is typically reduced by 25%, more particularly 50%, most particularly 70% compared to non-heat treated xanthan.
  • Xanthan gum native or heat treated, provides fixative properties to hair cosmetic compositions including hair sprays, gels including spray gels, styling lotions, creams, pomades, and mousses.
  • the use of xanthan gum imparts not only stiffness, but is also highly suitable for retention of curls under high humidity conditions.
  • High humidity conditions as used herein, is intended to mean at 22° C. and 90% relative humidity.
  • Xanthan gum is particularly suitable for gels as it provides clear to translucent clarity and is easy to use as it is dispersible in either hot or cold water and needs no neutralization. Xanthan gum also exhibits tolerance to salt and extreme pH, particularly in the range of about 2 to about 12. Finally, it is biodegradable and may be labeled as natural.
  • the heat modification of xanthan gum improves the ease of use, including the ease of dispersing in solution with less tendency to form fish eyes. Heat modification also may be used to improve thickening efficiency and gel texture, reducing the stringiness or pituitousness of the long texture. In addition, heat treatment of xanthan increases its viscosity throughout the pH and salt ranges typically used in hair cosmetic compositions. Unlike Carbomer, xanthan gum is compatible with anionic, cationic or nonionic polymers, allowing it to be formulated with a variety of commonly used hair cosmetic additives.
  • xanthan gum alone provides fixative properties, it may be used in combination with other fixatives, including without limitation polyoxythylenated vinyl acetate/crotonic acid copolymers, vinyl acetate crotonic acid (90/10) copolymers, vinyl acetate/crotonic acid/vinyl neodecanoate terpolymers, N-octylacrylamide/methylacrylate/hydroxypropyl methacrylate/acrylic acid/tert-butylaminoethyl methacrylate copolymers, and methyl vinyl ether/maleic anhydride (50/50) copolymers monoesterified with butanol or ethanol, acrylic acid/ethyl acrylate/N-tert-butyl-acrylamide terpolymers, and poly (methacrylic acid/acrylamidomethyl propane sulfonic acid), acrylates copolymer, octylacrylamide/acrylates/butylaminoethyl me
  • Optional conventional additives may also be incorporated into the hair compositions of this invention to provide certain modifying properties to the composition. Included among these additives are silicones and silicone derivatives; humectants; moisturizers; plasticizers, such as glycerine, glycol and phthalate esters and ethers; emollients, lubricants and penetrants, such as lanolin compounds; fragrances and perfumes; UV absorbers; dyes, pigments and other colorants; anticorrosion agents; antioxidants; detackifying agents; combing aids and conditioning agents; antistatic agents; neutralizers; glossifiers; preservatives; proteins, protein derivatives and amino acids; vitamins; emulsifiers; surfactants; viscosity modifiers, thickeners and rheology modifiers; gelling agents; opacifiers; stabilizers; sequestering agents; chelating agents; pearling agents; aesthetic enhancers; fatty acids, fatty alcohols and triglycerides;
  • Such additives are commonly used in hair cosmetic compositions known heretofore. These additives are present in small, effective amounts to accomplish their function, and generally will comprise from about 0.01 to 10% by weight each, and from about 0.01 to 20% by weight total, based on the weight of the composition.
  • Aesthetic enhancers is intended to include without limitation aluminum starch octenyl succinate, corn starch modified, aluminum starch octenylsuccinate (and) lauroyl lysine, and aluminum starch octenylsuccinate (and) boron nitride.
  • Thickeners and rheology modifiers is intended to include without limitation acrylates/steareth-20 itaconate copolymer, acrylates/ceteth-20 itaconate copolymer, potato starch modified, hydroxypropyl starch phosphate, acrylates/aminoacrylates/C10-30 alkyl PEG-20 itaconate copolymer, carbomer, acrylates/C10-30 alkyl acrylate crosspolymer, hydroxypropylcellulose, hydroxyethylcellulose, sodium carboxymethylcellulose, polyacrylamide (and) C13-14 isoparaffin (and) laureth-7, acrylamides copolymer (and) mineral oil (and) C13-14 isoparaffin (and) polysorbate 85, hydroxyethylacrylate/sodium acrylol dimethyltaurate copolymer, and hydroxyethylacrylate/sodium acrylol dimethyltaurate copolymer.
  • Xanthan gum may be formulated into hair cosmetic compositions at any level which provides the desired properties.
  • native xanthan gum will be used in an amount of at least about 0.01%, particularly at least about 0.2%, more particularly at least about 1.0% and less than about 20%, particularly less than about 10%, more particularly less than about about 3%.
  • heat treated xanthan gum will be used in an amount of at least about 0.01%, particularly at least about 0.5%, more particularly at least about 0.75% and less than about 20%, particularly less than about 2%, more particularly less than about 1.5%.
  • the amount used will depend not only upon the properties desired, but also upon the heat treatment levels and other additives. For example, the same amount of fixative property may be achieved by using less xanthan gum and adding another commonly used hair fixative polymer.
  • the hair cosmetic composition may be prepared by dispersing xanthan gum in water and then mixing in the remaining hair cosmetic components such as any fixative polymers, conditioning polymers or other additives as desired.
  • the delivery system in most cases will be water. However, it is possible to use a solvent. In general, the amount of solvent will be small to achieve a VOC (volatile organic compounds) content of no more than 55%.
  • the solvent will be a lower (C 1-4 ) alcohol, particularly methanol, ethanol, propanol, isopropanol, or butanol, though any solvent known in the art may be used.
  • VOC will also include any optional propellant(s).
  • the hair cosmetic composition may be formulated with xanthan gum to achieve the desired properties.
  • the amount of xanthan gum may be adjusted to achieve the desired stiffness and curl retention.
  • a hair gel will have a viscosity of at least about 5,000 cps, more particularly at least about 6,000 cps and most particularly at least about 8,000 cps, a high humidity curl retention for 2 hours of at least about 70%, more particularly at least about 80% and most particularly about 90%, and turbidity of no greater than 100 NTU, particularly no greater than 50 NTU, most particularly no greater than 30 NTU.
  • Formula 1 Formula 2 Ingredients % w/w % w/w Part A Acrylates Copolymer 1 (50%) 8.0 8.0.
  • Deionized Water 40.0 40.0 Aminomethyl Propanol 2 0.56 0.56
  • Xanthan gum 3 1.0 — Heat-treated Xanthan gum 4 — 1.0 Deionized Water q.s. q.s. Preservative q.s. q.s.
  • Part C Keratin Protein 0.2 0.2 Propylene Glycol 2.0 2.0 Polysorbate 20 5 0.5 0.5 Fragrance 0.1 0.1 100 100
  • part A The ingredients in part A were combined and mixed until clear.
  • xanthan or heat-treated xanthan gum was dispersed into water with moderate mixing (for formula 1, mix for 30 minutes at 700 rpm, and for formula 2, mix for 10 minutes at 700 rpm to achieve uniform part B).
  • Parts A and B were combined while stirring moderately and then part C was added.
  • both the xanthan and heat-treated xanthan gum were cold water dispersible. However, the heat-treated xanthan gum was easier to disperse than the native xanthan gum. In addition, no neutralization was needed with the use of xanthan gum.
  • Formula 1 produced a clear, colorless viscous liquid (Brookfield viscosity: 3200 cps with sprindle#4@20 rpm).
  • Formula 2 produced a clear, colorless gel (Brookfield viscosity: 8200 cps with sprindle#4@20 rpm).
  • Formula 2 had much higher viscosity than formula 1, which demonstrated that the heat-treated xanthan gum provides better thickening efficiency.
  • Formula 2 was also much more gel-like, or with shorter and less stringy gel texture compared to formula 1. Both formulas had very good clarity.
  • Formula 3 Formula 4 Formula 5 Formula 6
  • Ingredients % w/w % w/w % w/w % w/w % w/w % w/w Part A Acrylates Copolymer 1 (50%) 8.0 — — — — — Octylacrylamide/Acrylates/ — 4.0 — — — Butylaminoethyl Methacrylate Copolymer 2 Acrylates/Octylacrylamide — — 4.0 — — Copolymer 3 Octylacrylamide/Acrylates/ — — — 4.0 — Butylaminoethyl Methacrylate Copolymer 4 PVP 5 — — — — — 4.0 Deionized Water 40.0 40.0 40.0 40.0 40.0 40.0 Aminomethyl Propanol 6 0.56 0.94 1.13 0.77 — Part B Heat-treated Xanthan gum 7 0.85 0.85 0.85 0.85 — Carbomer 8
  • Formulas 3-6 produced clear to translucent hair gels with viscosity >7000 cps (Brookfield viscosity spindle #4@20 rpm).
  • formula 7 is a basic formula for the most commonly used commercial hair styling gel. This example shows the compatibility of various anionic fixative polymers with heat-treated xanthan gum.
  • Formula Formula Formula Formula 8 9 10 11 Ingredients % w/w % w/w % w/w % w/w % w/w Part A Acrylates Copolymer 1 (50%) 8.0 — — — Octylacrylamide/Acrylates/ — 4.0 — — Butylaminoethyl Methacrylate Copolymer 2 Acrylates/Octylacrylamide — — 4.0 — Copolymer 3 Octylacrylamide/Acrylates/ — — — 4.0 Butylaminoethyl Methacrylate Copolymer 4 Deionized Water 40.0 40.0 40.0 40.0 Aminomethyl Propanol 5 0.56 0.94 1.13 0.77 Part B Carbomer 6 0.5 0.5 0.5 0.5 0.5 Aminomethyl Propanol 0.29 0.29 0.29 0.29 Deionized Water q.s. q.s. q.s. Preservative q.s. q.s
  • Formulas 8-11 resulted in cloudy liquid mixtures with low viscosity. This demonstrates the incompatibility of various anionic fixative polymers with Carbomer.
  • Formula Formula Formula Formula 12 13 14 15 Ingredients % w/w % w/w % w/w % w/w % w/w Xanthan gum 2.0 — — — Heat-treated — 1.0 2.0 0.85 Xanthan gum Deionized Water q.s. q.s. q.s. q.s. Preservative q.s. q.s. q.s. q.s.s. 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100
  • Formulas 12-15 show that hair styling gels can simply contain xanthan gum or heat-treated xanthan gum at desired levels, as well as water and preservatives. Due to the improvement in solution rheology, heat-treated xanthan gum may be used at much lower level than untreated xanthan gum and produce more gel-like product.
  • Formula 21 Formula 22
  • Ingredients % w/w % w/w % w/w Part A Acrylates Copolymer 1 (50%) 8.0 4.0 8.0 Aminomethyl Propanol 0.56 0.28 0.56 Deionized Water 40.0 40.0 40.0 Part B
  • Heat-treated Xanthan gum 2 1.0 1.0 — Xanthan gum 3 — — 1.0 Deionized Water q.s. q.s. q.s Preservative q.s. q.s. q.s. 100 100 100 100 100
  • Formulas 26-30 show hair gels using xanthan gum samples that are heat-treated under different conditions.
  • Formula 31 Formula 32
  • Formula 33 Formula 34
  • Formula 36 Formula 37 Ingredients % w/w % w/w Part A Polyquaternium-4 1 0.15 — Polyquaternium-10 2 — 0.15 Deionized Water 40.0 40.0 Part B Heat-treated Xanthan gum 3 1.0 1.0 Deionized Water q.s. q.s. Preservative q.s. q.s. 100 100
  • Formulas 38-41 demonstrate that hair gels can be made by combining xanthan or heat-treated xanthan gum with other rheology modifiers/thickeners, such as Gellan gum or carbomer.
  • the curl retention properties of the hair styling compositions of the present invention were measured and compared to those of three leading commercial hair styling gel compositions with “ultimate” hair holding power. It is known to one skilled in the art that curl retention correlates directly to hair style retention, or hold, which is one of the most important performance attribute for a hair styling product.
  • the test was conducted at 72° F. (22° C.) and 90% Relative Humidity over a period of 2 hours. The procedure allows for statistical analysis of formulation variables.
  • Test 1 Subjective evaluation of hair styling compositions containing heat-treated xanthan gum compositions containing PVP and carbomer.
  • European dark brown hair tresses panelists (10′′long, 2 grams weight) with 0.5 grams of the hair styling composition were each rated by eight panelists by giving the samples a score of 1 (worst) to 5 (best) for a variety of properties.
  • the performance attributes tested included stiffness, wet feel, wet comb, dry gloss, dry feel, dry comb, dry flake, and anti-static. Stiffness is used to describe the hardness of hair body, which is also a measure of the amount of hold produced by hair styling compositions. This and similar types of sensory tests are well known by those in the art for the performance assessment of personal care and cosmetic products. A summary of the test results is shown in Table 2.
  • the overall performance of the hair compositions containing heat-treated xanthan gum was better or comparable to a PVP/carbomer hair gel in stiffness, gloss, dry comb, wet comb, flake, anti-static, and feel. All of the heat-treated xanthan gum containing gels provided better stiffness than the PVP/carbomer gel with the same amount of additional fixative polymers. Formula 1 also provided improved wet feel, wet comb, dry feel, and dry comb comparing to the PVP/carbomer gel.
  • Rank sums that differed by more than the least significant difference indicates samples which differed by more than 90% of what we would expect from guessing or random stimuli alone.
  • the hair tress preparation procedure was the same with that used in subjective Test 1.
  • a summary of the test results is shown in Table 3.
  • the higher rank run value indicates better performance on each attribute.
  • the differences in rank sum that were less than LSD (3.5) are considered as no significant difference at 90% confidence level.
  • This ranking test was designed for showing trends or patterns among the samples, but not particularly for the comparison of samples in pairs. Compared to the leading commercial gels, hair compositions containing xanthan gum, particularly heat-treated xanthan gum showed equivalent or better stiffness, gloss, and flake attributes.
  • a Rheometrics DSR SR-200 controlled stress rheometer was used for all measurements.
  • the crossover strain was obtained from an oscillatory shear stress sweep run at a frequency of 1 rad/s, from a stress of 2 to 1000 Pa at 25C.
  • the crossover strain was typically low for materials with short texture and high for materials with long, cohesive, or stringy textures.
  • the crossover strain data for selected hair gels is in Table 4.
  • the shortness of a leading commercial hair gel containing Carbomer and PVP was also measured as a comparison. Good agreement between the crossover strain data and subjective assessment of the gel texture has been found.
  • Table 4 the shortness of xanthan gel depended on the degree of heat treatment. The untreated xanthan gum gave more stringy and longer gel texture. The higher treatment temperature and/or longer treatment time tended to give shorter, less stringy gel texture. When appropriate heat treatment conditions were selected, one obtained significantly improved shorter gel texture, which was close to the most commonly used Carbomer gel (a polyacrylic acid thickener).
  • the clarity of hair gels were measured by using Hach Laboratory Turbidimeter (Model 2100N).
  • the instrument is designed for measurement of turbidity from 0 to 4000NTU (Nephelometric Turbidity Units) with automatic range selection and decimal point placement. Low turbidity reading represents high clarity.
  • the turbidity values of clear to translucent hair gels containing xanthan gum and heat-treated xanthan gum are listed in Table 5.
  • the turbidity values of three clear commercial hair gels are also listed as a reference.

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Abstract

The present invention is directed to the use of xanthan gum, particularly heat treated xanthan gum, as a fixative in hair cosmetic compositions. Xanthan gum is advantageous in that it may be used with other hair fixatives and provides rheology modifying and other properties including excellent stiffness, gloss, dry comb, wet comb, non-flake, anti-static, feel and high humidity curl retention.

Description

    BACKGROUND OF THE INVENTION
  • The present invention relates to the use of xanthan gum, particularly heat treated xanthan gum, as a fixative in hair cosmetic compositions and hair fixative compositions comprising xanthan gum. [0001]
  • Xanthan gum is a polysaccharide gum derived from the bacterium Xanthomonas and is well known in the art. It is composed of a main chain comprising β-(1,4) D-glucose units. Trisaccharide side chains on alternating anhydroglucose units are composed of a glucuronic acid residue between two mannose units. At most of the terminal mannose units is a pyruvate moiety and the non-terminal mannose carries an acetyl group. It has pseudoplastic or shear-thinning behavior characterized by a decrease in apparent viscosity in response to an increase in shear rate. [0002]
  • Xanthan gum is typically used in many industrial applications as a rheology modifier; thickening, viscosifying and gelling when combined with other polymers. It has also been used to impart stability to emulsions and prevent the settling out of solids. Its limited ability to disperse in either hot or cold water allows xanthan gum to be formulated into a broad variety of applications including pharmaceuticals, household products, foods, and personal care products. [0003]
  • Xanthan gum with an apparent average molecular weight of greater than 16,000,000 has been used to stabilize and improve the feel of emulsified cosmetics such as toilet water, creams and cleansing gels (JP Application No. 10-140503). [0004]
  • Xanthan gum which has been heat-treated is also known in the art. For example, EP 321 216 enhances the viscosity profile of xanthan gum by thermally treating it in the dry state (15% moisture or less). Heat treatment of xanthan gum is also known in JP Application No. 8-193055 which heat treats xanthan gum in the powdered form. [0005]
  • Surprisingly, it has now been discovered that xanthan gum, particularly heat treated xanthan gum, is a suitable fixative for hair cosmetic compositions. [0006]
  • SUMMARY OF THE INVENTION
  • The present invention is directed to the use of xanthan gum, particularly heat treated xanthan gum, as a fixative in hair cosmetic compositions. Xanthan gum is advantageous in that it may be used with other hair fixatives and provides rheology modifying and other properties including excellent stiffness, gloss, dry comb, wet comb, non-flake, anti-static, feel and high humidity curl retention. [0007]
  • DETAILED DESCRIPTION OF THE INVENTION
  • The present invention is directed to the use of xanthan gum, particularly heat treated xanthan gum, as a fixative in hair cosmetic compositions. [0008]
  • The xanthan gum may be used in a purified form or may be heat treated. Heat treatment of xanthan gum is typically done at low moisture, particularly less than about 25%, more particularly less than about 8%, most particularly less than about 1%, at a temperature of at least about 60° C., more particularly at least 100° C., and most particularly at least about 105° C. for a period of time of about 30 minutes, particularly at least one hour, more particularly at least 2.5 hours. [0009]
  • The moisture content, pH, temperature and time of heat treatment may be adjusted by one skilled in the art to achieve the viscosity, dispersibility, gel texture, solution clarity, and other properties desired. It will further be dependent upon the starting material used (grade, viscosity, molecular weight, and particle size). Typically, low moisture is used to improve the impact of heat-treatment. However, at any given moisture, increasing the temperature or time generally increases viscosity to a maximum and further heating decreases the viscosity of the xanthan gum at the concentrations used in this invention. Acidic pH are typically more suitable; a pH of 2-4 is most suitable. [0010]
  • Heat treatment of xanthan gum may be accomplished by a variety of methods known in the art including without limitation oven, fluidized bed, infrared and microwave heat treatments. The particle size of the resultant heat-treated xanthan gum may be adjusted using methods known in the art such as milling. [0011]
  • The xanthan gum may further be modified either before or after heat treatment. The xanthan gum may be converted by oxidation, enzyme conversion, acid hydrolysis, heat and/or acid dextrinization, or shear. The xanthan gum may also be chemically, enzymatically or physically modified. Suitable chemical derivatives include esters, such as the acetate, and half esters, such as the succinate, octenyl succinate and tetradecenyl succinate; phosphate derivatives; ethers such as hydroxyalkyl ethers and cationic ethers; or any other derivatives or combinations thereof. Modification may also be by chemical crosslinking. Crosslinking agents suitable for use herein include phosphorus oxychloride, epichlorohydrin, sodium trimetaphosphate and adipic-acetic mixed acid anyhrides. Such processes are also known in the art. Typically, the xanthan gum will not be modified other than by crosslinking or heat treatment. [0012]
  • The xanthan gum may also be purified by any method known in the art to remove off flavors and colors that are native to the xanthan gum or are created during the modification or heat treatment processes as long as the heat treatment is not substantially impacted. [0013]
  • The resultant heat-treated xanthan gum has improved dispersibility, such that under given conditions of temperature and agitation, the time to fully disperse the resultant gum is typically reduced by 25%, more particularly 50%, most particularly 70% compared to non-heat treated xanthan. [0014]
  • Xanthan gum, native or heat treated, provides fixative properties to hair cosmetic compositions including hair sprays, gels including spray gels, styling lotions, creams, pomades, and mousses. The use of xanthan gum imparts not only stiffness, but is also highly suitable for retention of curls under high humidity conditions. High humidity conditions, as used herein, is intended to mean at 22° C. and 90% relative humidity. [0015]
  • Xanthan gum is particularly suitable for gels as it provides clear to translucent clarity and is easy to use as it is dispersible in either hot or cold water and needs no neutralization. Xanthan gum also exhibits tolerance to salt and extreme pH, particularly in the range of about 2 to about 12. Finally, it is biodegradable and may be labeled as natural. [0016]
  • The heat modification of xanthan gum improves the ease of use, including the ease of dispersing in solution with less tendency to form fish eyes. Heat modification also may be used to improve thickening efficiency and gel texture, reducing the stringiness or pituitousness of the long texture. In addition, heat treatment of xanthan increases its viscosity throughout the pH and salt ranges typically used in hair cosmetic compositions. Unlike Carbomer, xanthan gum is compatible with anionic, cationic or nonionic polymers, allowing it to be formulated with a variety of commonly used hair cosmetic additives. Although xanthan gum alone provides fixative properties, it may be used in combination with other fixatives, including without limitation polyoxythylenated vinyl acetate/crotonic acid copolymers, vinyl acetate crotonic acid (90/10) copolymers, vinyl acetate/crotonic acid/vinyl neodecanoate terpolymers, N-octylacrylamide/methylacrylate/hydroxypropyl methacrylate/acrylic acid/tert-butylaminoethyl methacrylate copolymers, and methyl vinyl ether/maleic anhydride (50/50) copolymers monoesterified with butanol or ethanol, acrylic acid/ethyl acrylate/N-tert-butyl-acrylamide terpolymers, and poly (methacrylic acid/acrylamidomethyl propane sulfonic acid), acrylates copolymer, octylacrylamide/acrylates/butylaminoethyl methacrylate copolymer, acrylates/octylacrylamide copolymer, VA/crotonates/vinyl Neodeanoate copolymer, poly(N-vinyl acetamide), poly(N-vinyl formamide), corn starch modified, sodium polystyrene sulfonate, polyquaterniums such as polyquaternium-4, polyquaternium-7, polyquaternium-10, polyquaternium-11, polyquarternium-16, polyquaternium-28, polyquaternium-29, polyquaternium-46, polyether-1, polyurethanes, VA/acrylates/lauryl methacrylate copolymer, adipic acid/dimethylaminohydroxypropyl diethylene AMP/acrylates copolymer, methacrylol ethyl betaine/acrylates copolymer, PVP/dimethylaminoethylmethacrylate copolymer, PVP/DMAPA acrylates copolymer, PVP/vinylcaprolactam/DMAPA acrylates copolymer, vinyl caprolactam/PVP/dimethylaminoethyl methacrylate copolymer, VA/butyl maleate/isobornyl acrylate copolymer, VA/crotonates copolymer, acrylate/acrylamide copolymer, VA/crotonates/vinyl propionate copolymer, vinylpyrrolidone/vinyl acetate/vinyl propionate terpolymers, VA/crotonates, cationic and amphoteric guar, polyvinylpyrrolidone (PVP), polyvinylpyrrolidone/vinyl acetate copolymer, PVP acrylates copolymer, vinyl acetate/crotonic acid/vinyl proprionate, acrylates/acrylamide, acrylates/octylacrylamide, acrylates/hydroxyacrylates copolymer, and alkyl esters of polyvinylmethylether/maleic anhydride, diglycol/cyclohexanedimethanol/isophthalates/sulfoisophthalates copolymer, vinyl acetate/butyl maleate and isobornyl acrylate copolymer, vinylcaprolactamlPVP/dimethylaminoethyl methacrylate, vinyl acetatefalkylmaleate half ester/N-substituted acrylamide terpolymers, vinyl caprolactam/vinylpyrrolidonel methacryloamidopropyl trimethylammonium chloride terpolymer, methacrylates/acrylates copolymer/amine salt, polyvinylcaprolactam, polyurethanes, hydroxypropyl guar, hydroxypropyl guar hydroxypropyl trimmonium chloride, poly (methacrylic acid/acrylamidomethyl propane sulfonic acid, poylurethane/acrylate copolymers and hydroxypropyl trimmonium chloride guar, particularly acrylates copolymer, octylacrylamide/acrylates/butylaminoethyl methacrylate copolymer, acrylates/octylacrylamide copolymer, VA/crotonates/vinyl Neodeanoate copolymer, poly(N-vinyl acetamide), poly(N-vinyl formamide), polyurethane, corn starch modified, sodium polystyrene sulfonate, polyquaternium-4, polyquarternium-10, and polyurethane/acrylates copolymer. [0017]
  • Optional conventional additives may also be incorporated into the hair compositions of this invention to provide certain modifying properties to the composition. Included among these additives are silicones and silicone derivatives; humectants; moisturizers; plasticizers, such as glycerine, glycol and phthalate esters and ethers; emollients, lubricants and penetrants, such as lanolin compounds; fragrances and perfumes; UV absorbers; dyes, pigments and other colorants; anticorrosion agents; antioxidants; detackifying agents; combing aids and conditioning agents; antistatic agents; neutralizers; glossifiers; preservatives; proteins, protein derivatives and amino acids; vitamins; emulsifiers; surfactants; viscosity modifiers, thickeners and rheology modifiers; gelling agents; opacifiers; stabilizers; sequestering agents; chelating agents; pearling agents; aesthetic enhancers; fatty acids, fatty alcohols and triglycerides; botanical extracts; film formers; and clarifying agents. Such additives are commonly used in hair cosmetic compositions known heretofore. These additives are present in small, effective amounts to accomplish their function, and generally will comprise from about 0.01 to 10% by weight each, and from about 0.01 to 20% by weight total, based on the weight of the composition. [0018]
  • Aesthetic enhancers is intended to include without limitation aluminum starch octenyl succinate, corn starch modified, aluminum starch octenylsuccinate (and) lauroyl lysine, and aluminum starch octenylsuccinate (and) boron nitride. Thickeners and rheology modifiers is intended to include without limitation acrylates/steareth-20 itaconate copolymer, acrylates/ceteth-20 itaconate copolymer, potato starch modified, hydroxypropyl starch phosphate, acrylates/aminoacrylates/C10-30 alkyl PEG-20 itaconate copolymer, carbomer, acrylates/C10-30 alkyl acrylate crosspolymer, hydroxypropylcellulose, hydroxyethylcellulose, sodium carboxymethylcellulose, polyacrylamide (and) C13-14 isoparaffin (and) laureth-7, acrylamides copolymer (and) mineral oil (and) C13-14 isoparaffin (and) polysorbate 85, hydroxyethylacrylate/sodium acrylol dimethyltaurate copolymer, and hydroxyethylacrylate/sodium acrylol dimethyltaurate copolymer. [0019]
  • Xanthan gum may be formulated into hair cosmetic compositions at any level which provides the desired properties. Typically, native xanthan gum will be used in an amount of at least about 0.01%, particularly at least about 0.2%, more particularly at least about 1.0% and less than about 20%, particularly less than about 10%, more particularly less than about about 3%. In contrast, heat treated xanthan gum will be used in an amount of at least about 0.01%, particularly at least about 0.5%, more particularly at least about 0.75% and less than about 20%, particularly less than about 2%, more particularly less than about 1.5%. The amount used will depend not only upon the properties desired, but also upon the heat treatment levels and other additives. For example, the same amount of fixative property may be achieved by using less xanthan gum and adding another commonly used hair fixative polymer. [0020]
  • The hair cosmetic composition may be prepared by dispersing xanthan gum in water and then mixing in the remaining hair cosmetic components such as any fixative polymers, conditioning polymers or other additives as desired. [0021]
  • The delivery system in most cases will be water. However, it is possible to use a solvent. In general, the amount of solvent will be small to achieve a VOC (volatile organic compounds) content of no more than 55%. Typically, the solvent will be a lower (C[0022] 1-4) alcohol, particularly methanol, ethanol, propanol, isopropanol, or butanol, though any solvent known in the art may be used. VOC will also include any optional propellant(s).
  • The hair cosmetic composition may be formulated with xanthan gum to achieve the desired properties. For example the amount of xanthan gum may be adjusted to achieve the desired stiffness and curl retention. In general, a hair gel will have a viscosity of at least about 5,000 cps, more particularly at least about 6,000 cps and most particularly at least about 8,000 cps, a high humidity curl retention for 2 hours of at least about 70%, more particularly at least about 80% and most particularly about 90%, and turbidity of no greater than 100 NTU, particularly no greater than 50 NTU, most particularly no greater than 30 NTU.[0023]
  • EXAMPLES
  • The following examples are presented to further illustrate and explain the present invention and should not be taken as limiting in any regard. All percents used are on a weight/weight basis. [0024]
  • Example 1 Hair Styling Gels with Native and Heat-Treated Xanthan Gum
  • [0025]
    Formula 1 Formula 2
    Ingredients % w/w % w/w
    Part A
    Acrylates Copolymer1 (50%) 8.0 8.0.
    Deionized Water 40.0 40.0
    Aminomethyl Propanol2 0.56 0.56
    Part B
    Xanthan gum3 1.0
    Heat-treated Xanthan gum4 1.0
    Deionized Water q.s. q.s.
    Preservative q.s. q.s.
    Part C
    Keratin Protein 0.2 0.2
    Propylene Glycol 2.0 2.0
    Polysorbate 205 0.5 0.5
    Fragrance 0.1 0.1
    100 100
  • The ingredients in part A were combined and mixed until clear. In a separate container, xanthan or heat-treated xanthan gum was dispersed into water with moderate mixing (for formula 1, mix for 30 minutes at 700 rpm, and for formula 2, mix for 10 minutes at 700 rpm to achieve uniform part B). Parts A and B were combined while stirring moderately and then part C was added. [0026]
  • Both the xanthan and heat-treated xanthan gum were cold water dispersible. However, the heat-treated xanthan gum was easier to disperse than the native xanthan gum. In addition, no neutralization was needed with the use of xanthan gum. [0027]
  • Formula 1 produced a clear, colorless viscous liquid (Brookfield viscosity: 3200 cps with sprindle#4@20 rpm). Formula 2 produced a clear, colorless gel (Brookfield viscosity: 8200 cps with sprindle#4@20 rpm). Formula 2 had much higher viscosity than formula 1, which demonstrated that the heat-treated xanthan gum provides better thickening efficiency. Formula 2 was also much more gel-like, or with shorter and less stringy gel texture compared to formula 1. Both formulas had very good clarity. [0028]
  • Example 2 Various Hair Styling Gel Formulations
  • [0029]
    Formula 3 Formula 4 Formula 5 Formula 6 Formula 7
    Ingredients % w/w % w/w % w/w % w/w % w/w
    Part A
    Acrylates Copolymer1 (50%) 8.0
    Octylacrylamide/Acrylates/ 4.0
    Butylaminoethyl Methacrylate
    Copolymer2
    Acrylates/Octylacrylamide 4.0
    Copolymer3
    Octylacrylamide/Acrylates/ 4.0
    Butylaminoethyl Methacrylate
    Copolymer4
    PVP5 4.0
    Deionized Water 40.0 40.0 40.0 40.0 40.0
    Aminomethyl Propanol6 0.56 0.94 1.13 0.77
    Part B
    Heat-treated Xanthan gum7 0.85 0.85 0.85 0.85
    Carbomer8 0.5
    Aminomethyl Propanol 0.29
    Deionized Water q.s. q.s. q.s. q.s. q.s.
    Preservative q.s. q.s. q.s. q.s. q.s.
    100 100 100 100 100
  • Formulas 3-6 produced clear to translucent hair gels with viscosity >7000 cps (Brookfield viscosity spindle #4@20 rpm). As a comparison, formula 7 is a basic formula for the most commonly used commercial hair styling gel. This example shows the compatibility of various anionic fixative polymers with heat-treated xanthan gum. [0030]
    Formula Formula Formula Formula
    8 9 10 11
    Ingredients % w/w % w/w % w/w % w/w
    Part A
    Acrylates Copolymer1 (50%) 8.0
    Octylacrylamide/Acrylates/ 4.0
    Butylaminoethyl Methacrylate
    Copolymer2
    Acrylates/Octylacrylamide 4.0
    Copolymer3
    Octylacrylamide/Acrylates/ 4.0
    Butylaminoethyl Methacrylate
    Copolymer4
    Deionized Water 40.0 40.0 40.0 40.0
    Aminomethyl Propanol5 0.56 0.94 1.13 0.77
    Part B
    Carbomer6 0.5 0.5 0.5 0.5
    Aminomethyl Propanol 0.29 0.29 0.29 0.29
    Deionized Water q.s. q.s. q.s. q.s.
    Preservative q.s. q.s. q.s. q.s.
    100 100 100 100
  • Formulas 8-11 resulted in cloudy liquid mixtures with low viscosity. This demonstrates the incompatibility of various anionic fixative polymers with Carbomer. [0031]
    Formula Formula Formula Formula
    12 13 14 15
    Ingredients % w/w % w/w % w/w % w/w
    Xanthan gum 2.0
    Heat-treated 1.0 2.0 0.85
    Xanthan gum
    Deionized Water q.s. q.s. q.s. q.s.
    Preservative q.s. q.s. q.s. q.s.
    100 100 100 100
  • Formulas 12-15 show that hair styling gels can simply contain xanthan gum or heat-treated xanthan gum at desired levels, as well as water and preservatives. Due to the improvement in solution rheology, heat-treated xanthan gum may be used at much lower level than untreated xanthan gum and produce more gel-like product. [0032]
    Formula 21 Formula 22 Formula 23
    Ingredients % w/w % w/w % w/w
    Part A
    Acrylates Copolymer1 (50%) 8.0 4.0 8.0
    Aminomethyl Propanol 0.56 0.28 0.56
    Deionized Water 40.0 40.0 40.0
    Part B
    Heat-treated Xanthan gum2 1.0 1.0
    Xanthan gum3 1.0
    Deionized Water q.s. q.s. q.s
    Preservative q.s. q.s. q.s.
    100 100 100
  • These formulas further show different combinations of xanthan and heat-treated xanthan gum with anionic and nonionic fixative polymers at different use levels. [0033]
    Formula 26 Formula 27 Formula 28 Formula 29 Formula 30
    Ingredients % w/w % w/w % w/w % w/w % w/w
    Part A
    Acrylates Copolymer1 (50%) 8.0 8.0 8.0 8.0 8.0
    Aminomethyl Propanol 0.56 0.56 0.56 0.56 0.56
    Deionized Water 40.0 40.0 40.0 40.0 40.0
    Part B
    Heat-treated Xanthan gum2 1.0
    Heat-treated Xanthan gum3 1.0
    Heat-treated Xanthan gum4 1.0
    Heat-treated Xanthan gum5 1.0
    Heat-treated Xanthan gum6 1.0
    Deionized Water q.s. q.s. q.s. q.s. q.s.
    Preservative q.s. q.s. q.s. q.s. q.s.
    100 100 100 100 100
  • Formulas 26-30 show hair gels using xanthan gum samples that are heat-treated under different conditions. [0034]
    Formula 31 Formula 32 Formula 33 Formula 34 Formula 35
    Ingredients % w/w % w/w % w/w % w/w % w/w
    Part A
    Poly (N-vinyl acetamide) 3.0 1.0
    Poly (N-vinyl formamide) 3.0
    Polyurethane 3.0
    Corn Starch Modified1 1.0
    Deionized Water 40.0 40.0 40.0 40.0 40.0
    Part B
    Heat-treated Xanthan gum2 1.0 1.0 1.0 1.0 1.0
    Deionized Water q.s. q.s. q.s. q.s. q.s.
    Preservative q.s. q.s. q.s. q.s. q.s.
    100 100 100 100 100
  • These examples show hair gels made with heat-treated xanthan gum and various fixative polymers at different use levels. [0035]
    Formula 36 Formula 37
    Ingredients % w/w % w/w
    Part A
    Polyquaternium-41 0.15
    Polyquaternium-102 0.15
    Deionized Water 40.0 40.0
    Part B
    Heat-treated Xanthan gum3 1.0 1.0
    Deionized Water q.s. q.s.
    Preservative q.s. q.s.
    100 100
  • These formulas show that cationic fixative/conditioning polymers can be used at lower levels with heat-treated xanthan gum to produce clear hair gels with good performance and rheology. [0036]
    Formula Formula Formula Formula
    38 39 40 41
    Ingredients % w/w % w/w % w/w % w/w
    Part A
    Gellan Gum1 0.3 0.3
    Carbomer2 0.1 0.3
    Deionized Water 40.0 40.0 40.0 40.0
    Aminomethyl Propanol3 q.s. to q.s. to
    pH 6 pH 6
    Part B
    Heat-treated Xanthan gum4 1.0 1.0
    Xanthan gum5 1.0 1.0
    Deionized Water q.s. q.s. q.s. q.s.
    Preservative q.s. q.s. q.s. q.s.
    100 100 100 100
  • Formulas 38-41 demonstrate that hair gels can be made by combining xanthan or heat-treated xanthan gum with other rheology modifiers/thickeners, such as Gellan gum or carbomer. [0037]
  • Example 3 Hair Styling Gel Performance (I) and Curl Retention
  • The curl retention properties of the hair styling compositions of the present invention were measured and compared to those of three leading commercial hair styling gel compositions with “ultimate” hair holding power. It is known to one skilled in the art that curl retention correlates directly to hair style retention, or hold, which is one of the most important performance attribute for a hair styling product. The test was conducted at 72° F. (22° C.) and 90% Relative Humidity over a period of 2 hours. The procedure allows for statistical analysis of formulation variables. The percentage curl retention was calculated by: Curl Retention %=100×(L−L[0038] t)/(L−Lo). where L=iength of hair fully extended, Lo=initial curl length, Lt=curl length at a givin time t.
  • The test was performed on 10″ long×2 gram tresses of European virgin brown hair (9 replicate tresses per sample). Cleaned wet hair tresses were combed through to remove tangles and excess water is removed. 0.5 gram of sample hair gel was applied to each tress, gently “worked into” the hair tress and combed through. Curls of hair were made using ½″ diameter Teflon mandrel, placed on a tray and dried in an oven overnight. The dried curls were removed from the oven and allowed to cool to room temperature. The curls were suspended from the bound end of the tress on graduated transparent curl retention boards. An initial curl length reading was taken before placing boards and curls into the environment chamber. Then curl lengths were recorded at 15 minutes, 30 minutes, 60 minutes, 90 minutes and 2 hours. Curl retention averages were then calculated. [0039]
  • The curl retention results after 2 hours are tabulated in Table 1. The results demonstrate that all the hair styling compositions containing xanthan gum, particularly heat-treated xanthan gum, exhibited dramatically superior curl retention compared to the leading commercial products. This superior curl retention property was achieved with and without other fixative polymers. The type and amount of additional fixative polymers did not vary the curl retention capability significantly with xanthan or heat-treated xanthan gum present. Significantly lower curl retention results were obtained when carbomer is used in the composition instead of xanthan gum, particularly heat-treated xanthan gum. [0040]
    TABLE 1
    Average % Curl Retention
    Time = 2 hours
    Hair Styling Gel Compositions T = 72° F.; RH = 90%
    1% heat-treated xanthan gum (Formula 13) 91
    2% heat-treated xanthan gum (Formula 12) 93
    4% Acrylates Copolymer + 93
    1% heat-treated xanthan gum (Formula 21)
    4% Acrylates Copolymer + 91
    1% untreated xanthan gum (Formula 23)
    2% Acrylates Copolymer + 89
    1% heat-treated xanthan gum (Formula 22)
    3% PVP + 95
    1% heat-treated xanthan gum (Formula 18)
    4% PVP + 84
    1% heat-treated xanthan gum (Formula 17)
    4% PVP + 48
    0.5% Carbomer (Formula 16)
    3% Poly (N-vinyl acetamide) + 93
    1% heat-treated xanthan gum (Formula 31)
    1% Poly (N-vinyl acetamide) + 91
    1% heat-treated xanthan gum (Formula 32)
    Commercial hair gel I (containing PVP, 34
    carbomer, and other additives)
    Commercial hair gel II (containing PVP/VA 47
    copolymer, carbomer, and other additives)
    Commercial hair gel III (containing PVP/VA 11
    copolymer, PVP, carbomer, and other
    additives)
  • Example 4 Hair Styling Gel Performance, Stiffness and Other Attributes
  • Test 1—Subjective evaluation of hair styling compositions containing heat-treated xanthan gum compositions containing PVP and carbomer. European dark brown hair tresses panelists (10″long, 2 grams weight) with 0.5 grams of the hair styling composition were each rated by eight panelists by giving the samples a score of 1 (worst) to 5 (best) for a variety of properties. The performance attributes tested included stiffness, wet feel, wet comb, dry gloss, dry feel, dry comb, dry flake, and anti-static. Stiffness is used to describe the hardness of hair body, which is also a measure of the amount of hold produced by hair styling compositions. This and similar types of sensory tests are well known by those in the art for the performance assessment of personal care and cosmetic products. A summary of the test results is shown in Table 2. [0041]
  • The overall performance of the hair compositions containing heat-treated xanthan gum was better or comparable to a PVP/carbomer hair gel in stiffness, gloss, dry comb, wet comb, flake, anti-static, and feel. All of the heat-treated xanthan gum containing gels provided better stiffness than the PVP/carbomer gel with the same amount of additional fixative polymers. Formula 1 also provided improved wet feel, wet comb, dry feel, and dry comb comparing to the PVP/carbomer gel. [0042]
    TABLE 2
    Results of Subjective Test 1
    Average score based on 1 (worst) to 5 (best) rating scale
    Formula 7
    Attribute Formula 3 Formula 4 Formula 5 (control)
    wet feel 3.8 S 2.7 NS 2.8 NS 2.8
    wet comb 3.8 S 2.5 NS 2.6 NS 2.9
    dry gloss 3.4 NS 2.7 NS 3.1 NS 3.2
    Stiffness 3.8 S 3.6 S 3.6 S 2.3
    dry comb 3.9 S 2.8 NS 2.7 NS 3.2
    dry flake 2.8 NS 3.0 NS 3.1 NS 3.2
    anti-static 1.9 NS 2.1 NS 2.2 NS 2.1
    dry feel 3.4 S 2.9 NS 2.7 NS 2.7
  • Test 2 [0043]
  • Subjective ranking of six hair styling compositions and three leading commercial hair styling gels was performed on human hair tresses for the performance attributes of stiffness, gloss, and dry flake. This sensory evaluation used a Balanced Incomplete Block Design, with which ranking is based on the intensity of attributes. Nine samples were ranked in groups of two by nine panelists. For each pair of samples, a score of 1 was given for less stiffness, more dry flake, and less gloss, and a score of 2 was given for more stiffness, less dry flake, and more gloss. Based on the design, a total of 36 blocks (or pairs) of samples were prepared. The ranking sum of each attribute for each sample was calculated. Rank sums that differed by more than the least significant difference (LSD=3.5) indicates samples which differed by more than 90% of what we would expect from guessing or random stimuli alone. The hair tress preparation procedure was the same with that used in subjective Test 1. A summary of the test results is shown in Table 3. The higher rank run value indicates better performance on each attribute. The differences in rank sum that were less than LSD (3.5) are considered as no significant difference at 90% confidence level. This ranking test was designed for showing trends or patterns among the samples, but not particularly for the comparison of samples in pairs. Compared to the leading commercial gels, hair compositions containing xanthan gum, particularly heat-treated xanthan gum showed equivalent or better stiffness, gloss, and flake attributes. [0044]
    TABLE 3
    Results of Subjective Test 2
    Rank Sums (LSD = 3.5)
    Hair Styling Gel Compositions Stiffness Gloss Flake
    Commercial hair gel I (containing PVP, 12 11 12
    carbomer, and other additives)
    Commercial hair gel II (containing PVP/VA 11 12 12
    copolymer, carbomer, and other additives)
    Commercial hair gel III (containing PVP/VA 8 12 9
    copolymer, PVP, carbomer, and other
    additives)
    4% PVP + 0.5% Carbomer (Formula 16) 15 9 10
    4% PVP + 15 13 11
    1% heat-treated xanthan gum (Formula 17)
    4% Acrylates Copolymer + 11 11 15
    1% heat-treated xanthan gum (Formula 21)
    1% heat-treated xanthan gum (Formula 13) 11 15 13
    2% Acrylates Copolymer + 12 12 14
    1% heat-treated xanthan gum (Formula 22)
    4% Acrylates Copolymer + 13 13 12
    1% untreated xanthan gum (Formula 23)
  • Example 5 Measurement of Gel Texture
  • A Rheometrics DSR SR-200 controlled stress rheometer was used for all measurements. The crossover strain was obtained from an oscillatory shear stress sweep run at a frequency of 1 rad/s, from a stress of 2 to 1000 Pa at 25C. The tangent of the phase angle, tandelta was plotted versus the strain amplitude and the crossover strain was defined as the strain at which the tand=1. This method was applied only to materials which had values of tandelta<1 at low stresses and which then broke down and had values greater than 1 at high stresses. The crossover strain was typically low for materials with short texture and high for materials with long, cohesive, or stringy textures. The crossover strain data for selected hair gels is in Table 4. The shortness of a leading commercial hair gel containing Carbomer and PVP was also measured as a comparison. Good agreement between the crossover strain data and subjective assessment of the gel texture has been found. As shown in Table 4, the shortness of xanthan gel depended on the degree of heat treatment. The untreated xanthan gum gave more stringy and longer gel texture. The higher treatment temperature and/or longer treatment time tended to give shorter, less stringy gel texture. When appropriate heat treatment conditions were selected, one obtained significantly improved shorter gel texture, which was close to the most commonly used Carbomer gel (a polyacrylic acid thickener). [0045]
    TABLE 4
    Hair Styling Gel Compositions Crossover Strain (%)
    4% Acrylates Copolymer + 155
    1% untreated xanthan gum (Formula 23)
    4% Acrylates Copolymer + 131
    1% heat-treated xanthan gum (fluid bed
    @220° F. for 120 minutes)
    4% Acrylates Copolymer + 88
    1% heat-treated xanthan gum (fluid bed
    @220° F. for 150 minutes)
    4% Acrylates Copolymer + 150
    1% heat-treated xanthan gum (fluid bed
    @228° F. for 60 minutes)
    4% Acrylates Copolymer + 120
    1% heat-treated xanthan gum (fluid bed
    @228° F. for 90 minutes)
    4% Acrylates Copolymer + 96
    1% heat-treated xanthan gum (fluid bed
    @235° F. for 60 minutes)
    1% heat-treated xanthan gum (fluid bed 82
    @235° F. for 60 minutes)
    Commercial hair gel (containing PVP, 73
    carbomer, and other additives)
  • Example 6 Clarity Measurement of Hair Gels
  • The clarity of hair gels were measured by using Hach Laboratory Turbidimeter (Model 2100N). The instrument is designed for measurement of turbidity from 0 to 4000NTU (Nephelometric Turbidity Units) with automatic range selection and decimal point placement. Low turbidity reading represents high clarity. The turbidity values of clear to translucent hair gels containing xanthan gum and heat-treated xanthan gum are listed in Table 5. The turbidity values of three clear commercial hair gels are also listed as a reference. [0046]
    TABLE 5
    Hair Styling Gel Compositions Turbidity (NTU)
    4% Acrylates Copolymer + 18.5
    1% untreated xanthan gum (Formula 19)
    4% Acrylates Copolymer + 24.2
    1% heat-treated xanthan gum (fluid bed
    @220° F. for 120 minutes)
    4% Acrylates Copolymer + 25.2
    1% heat-treated xanthan gum (fluid bed
    @220° F. for 150 minutes)
    4% Acrylates Copolymer + 23.7
    1% heat-treated xanthan gum (fluid bed
    @228° F. for 60 minutes)
    4% Acrylates Copolymer + 24.5
    1% heat-treated xanthan gum (fluid bed
    @228° F. for 90 minutes)
    4% Acrylates Copolymer + 25.3
    1% heat-treated xanthan gum (fluid bed
    @235° F. for 60 minutes)
    1% heat-treated xanthan gum (fluid bed 24.2
    @235° F. for 60 minutes)
    Commercial hair gel (containing PVP, PVP/VA, 15.0
    carbomer, and other additives)
    Commercial hair gel (containing PVP, 14.0
    carbomer, and other additives)
    Commercial hair gel (containing PVP, 10.9
    carbomer, and other additives)
    Deionized water 0.04
  • Example 7 Hair Spray Gel with Xanthan Gum
  • [0047]
    Ingredients % w/w % w/w
    Part A
    Acrylates Copolymer1 (50%) 8.0 8.0.
    D.I. Water 40.0 40.0
    Aminomethyl Propanol2 0.56 0.56
    Part B
    Xanthan gum3 0.5
    Heat-treated Xanthan gum4 0.3
    Deionized Water q.s. q.s.
    Preservative q.s. q.s.
    Part C
    Keratin Protein 0.2 0.2
    Propylene Glycol 2.0 2.0
    Polysorbate 204 0.5 0.5
    Fragrance 0.1 0.1
  • Example 8 Surfactant-Free Hair Mousse with Xanthan Gum
  • [0048]
    Ingredients % w/w
    Acrylates Copolymer1 (50%) 8.0
    D.I. Water 40.0
    Aminomethyl Propanol2 0.56
    Xanthan gum3 0.4
    Deionized Water q.s.
    Preservative q.s.
    Part C
    Isobutane/Propane4 6.0
    100
  • Example 9 Styling Mousse
  • [0049]
    Ingredients % w/w
    Sodium Polystyrene Sulfonate1 10.0
    Polysorbate 202 0.4
    Nonoxynol-153 0.4
    Oleth-104 0.4
    Xanthan gum5 0.5
    Deionized Water 68.3
    SD Alcohol 40 10.0
    Isobutane 10.0
    100
  • Example 10 Aerosol Hair Spray
  • [0050]
    Ingredients % w/w
    Octylacrylamide/Acrylates/ 8.0
    Butylaminoethyl Methacrylate
    Copolymer1
    Aminomethyl Propanol2 1.38
    Xanthan gum3 0.3
    Deionized Water 45.32
    SD Alcohol 40 20.0
    Fragrance q.s.
    Preservative q.s.
    Dimethyl Ether 25.0
    100
  • Example 11 Hair Styling and Conditioning Cream
  • [0051]
    Ingredients % w/w
    Part A
    Deionized Water q.s.
    Heat-treated xanthan gum1 0.7
    Quaternium-42 0.15
    Part B
    Glyceryl Stearate3 2.0
    Jojoba oil 2.0
    Part C
    Fragrance q.s.
    Preservative g.s.
    100

Claims (22)

We claim:
1. A hair cosmetic composition comprising a fixative effective amount of xanthan gum.
2. The composition of claim 1, wherein the xanthan gum has been heat treated at a moisture content of less than about 25%, a temperature of at least about 60° C. for at least about 30 minutes.
3. The composition of claim 2, wherein the temperature is at least 100° C.
4. The composition of claim 3, wherein the temperature is at least 105° C.
5. The composition of claim 2, wherein the moisture content is less than about 8%.
6. The composition of claim 3, wherein the moisture content is less than about 1%.
7. The composition of claim 2, wherein the heat treatment is for at least about one hour.
8. The composition of claim 3, wherein the heat treatment is for at least about 2.5 hours.
9. The composition of claim 2, wherein the heat treatment is at a moisture of less than about 1% and the temperature is at least about 105° C. for at least about 2.5 hours.
10. The composition of claim 1, wherein the composition is selected from the group consisting of a spray, a mousse, a hair lotion, a cream, a pomade, and a gel.
11. The composition of claim 10, wherein the composition is a gel.
12. The composition of claim 13 characterized by a viscosity of at least about 8000 cps, a high humidity curl retention of at least about (80%) and a turbidity of no more than about 100 NTU.
13. The composition of claim 1, further comprising a second fixative polymer.
14. The composition of claim 13 wherein the second fixative polymer is selected from the group comprising acrylates copolymer, octylacrylamide/acrylates/butylaminoethyl methacrylate copolymer, acrylates/octylacrylamide copolymer, VA/crotonates/vinyl Neodeanoate copolymer, poly(N-vinyl acetamide), poly(N-vinyl formamide), polyurethane, corn starch modified, sodium polystyrene sulfonate, polyquaternium-4, polyquaternium-10 and polurethane/acrylates copolymer.
15. The composition of claim 2, wherein the composition is a gel.
16. The composition of claim 16 further comprising a second fixative polymer.
17. The composition of claim 17 wherein the second fixative polymer is selected from the group comprising acrylates copolymer, octylacrylamide/acrylates/butylaminoethyl methacrylate copolymer, acrylates/octylacrylamide copolymer, VA/crotonates/vinyl Neodeanoate copolymer, poly(N-vinyl acetamide), poly(N-vinyl formamide), polyurethane, corn starch modified, sodium polystyrene sulfonate, polyquaternium-4, polyquaternium-10 and polyurethane/acrylates copolymer.
18. A method of preparing the composition of claim 1, comprising dispersing the xanthan gum in water; and mixing in other hair cosmetic components.
19. A method of preparing the composition of claim 2, comprising dispersing the xanthan gum in water; and mixing in other hair cosmetic components.
20. A method of preparing the composition of claim 17 comprising dispersing the xanthan gum in water; and mixing in other hair cosmetic components.
21. A method of providing fixative properties to the hair comprising applying the composition of claim 1.
22. A method of providing curl retention under high humidity conditions comprising applying the composition of claim 1.
US09/932,435 2001-08-17 2001-08-17 Use of xanthan gum as a hair fixative Abandoned US20030108505A1 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
US09/932,435 US20030108505A1 (en) 2001-08-17 2001-08-17 Use of xanthan gum as a hair fixative
US10/198,469 US9072683B2 (en) 2001-08-17 2002-07-18 Use of xanthan gum as a hair fixative
DE10237257A DE10237257A1 (en) 2001-08-17 2002-08-14 Use of xanthan gum as a hair fixative
GB0218928A GB2380938B (en) 2001-08-17 2002-08-14 Use of xanthan gum as a hair fixative
MXPA02007911A MXPA02007911A (en) 2001-08-17 2002-08-15 Use of xanthan gum as a hair fixative.
JP2002236931A JP4920854B2 (en) 2001-08-17 2002-08-15 Use of xanthan gum as a hair fixative
FR0210368A FR2828645B1 (en) 2001-08-17 2002-08-16 HAIR COSMETIC COMPOSITION CONTAINING XANTHAN GUM, AND PROCESS FOR PREPARING THE SAME
CNB021437351A CN100482205C (en) 2001-08-17 2002-08-16 Application for xanthan gum as hair appoving agent
BR0203284-8A BR0203284A (en) 2001-08-17 2002-08-19 Cosmetic makeup for hair and method of preparing it
JP2008121664A JP5511151B2 (en) 2001-08-17 2008-05-07 Use of xanthan gum as a hair fixative

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030143179A1 (en) * 2001-08-17 2003-07-31 Hongjie Cao Use of xanthan gum as a hair fixative
US20050255067A1 (en) * 2004-05-17 2005-11-17 Leighton John C Hair fixative film
US20080085255A1 (en) * 2006-10-06 2008-04-10 L'oreal Aqueous fatty monoamine-containing anti-frizz composition for hair
US20080131469A1 (en) * 2003-05-14 2008-06-05 National Starch And Chemical Inverstment Holding Corporation Aqueous composition for cosmetics and cosmetic including the same
US20080181858A1 (en) * 2007-01-31 2008-07-31 National Starch And Chemical Investment Holding Corporation Sunscreen Compositions
KR101048382B1 (en) * 2004-03-15 2011-07-11 주식회사 엘지생활건강 Spray cosmetic composition that improves the durability of makeup cosmetics without stickiness
US20110212145A1 (en) * 2010-03-01 2011-09-01 Honeywell International Inc. Hair fixatives comprising cross linked starches
US8545828B1 (en) 2003-02-21 2013-10-01 Akzo Nobel N. V. High viscosity heat-treated xanthan gum
US20150136167A1 (en) * 2012-05-21 2015-05-21 Conopco, Inc., D/B/A Unilever Method of treating hair
WO2016081465A1 (en) * 2014-11-20 2016-05-26 The Procter & Gamble Company Hair care compositions comprising dehydroxanthan gum
WO2019115706A1 (en) * 2017-12-14 2019-06-20 L'oreal Monophasic appearance cosmetic hair composition comprising a particular non-ionic surfactant
US10588839B2 (en) 2013-11-21 2020-03-17 Conopco, Inc. Method of shaping hair
US10617615B2 (en) 2013-11-21 2020-04-14 Conopco, Inc. Method of treating hair

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8399001B2 (en) * 2003-11-18 2013-03-19 L'oreal Cosmetic composition comprising at least one gellan gum or derivative thereof, at least one monovalent salt, and at least one suspension compound, processes using this composition, and uses thereof
DE10358780A1 (en) * 2003-12-12 2005-07-14 Hans Schwarzkopf & Henkel Gmbh & Co. Kg Sprayable gel
US7378382B2 (en) * 2004-05-05 2008-05-27 The Clorox Company Rheologically stabilized silicone dispersions comprising a polydimethylsiloxane mixture
GB2423252B (en) * 2005-02-18 2007-10-17 Engelhard Lyon Cross-linked polymer of carbohydrate, notably based on polysaccharides, and/or on oligosaccharides and/or on polyols
US11938213B2 (en) 2019-09-30 2024-03-26 L'oreal Hair cosmetic compositions containing cationic polymers, acrylate-based polymers, gums, and polyols
WO2024097166A1 (en) 2022-11-02 2024-05-10 Nutrition & Biosciences USA 4, Inc. Compositions comprising xanthan gum and crystalline alpha-1,3-glucan

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3349077A (en) * 1965-05-17 1967-10-24 Kelco Co Etherified xanthomonas hydrophilic colloids and process of preparation
US4591610A (en) * 1983-03-23 1986-05-27 L'oreal Thickened or gelled composition for conditioning hair
US5198469A (en) * 1990-12-11 1993-03-30 Shigenobu Sakata Bath lotion and body lotion with pharmaceutical effect

Family Cites Families (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4477480A (en) * 1982-07-06 1984-10-16 General Foods Corporation Method of preparing a clean flavored cereal starch
US4465702A (en) * 1982-11-01 1984-08-14 A. E. Staley Manufacturing Company Cold-water-soluble granular starch for gelled food compositions
US4595586A (en) * 1985-08-30 1986-06-17 Eli Lilly And Company Moisturizing lotion
JPS62263111A (en) 1986-05-09 1987-11-16 Shiseido Co Ltd Viscous composition
JPH0615460B2 (en) 1986-12-12 1994-03-02 花王株式会社 Hair cosmetics
EP0321216A3 (en) 1987-12-17 1989-08-23 Kenneth R. Stauffer Method of enhancing the v1/v2 viscosity profile of xanthan
US5131953A (en) * 1988-09-12 1992-07-21 National Starch And Chemical Investment Holding Corporation Continuous coupled jet-cooking/spray-drying process and novel pregelatinized high amylose starches prepared thereby
US5149799A (en) * 1990-01-26 1992-09-22 National Starch And Chemical Investment Holding Corporation Method and apparatus for cooking and spray-drying starch
US5037929A (en) * 1990-08-22 1991-08-06 Kansas State University Research Found. Process for the preparation of granular cold water-soluble starch
CA2068124A1 (en) * 1991-05-24 1992-11-25 Daniel J. Halloran Optically clear hair care compositions containing amino-functional silicone microemulsions
US5187272A (en) * 1992-01-21 1993-02-16 Kraft General Foods, Inc. Process for preparing non-hydroxypropylated, deflavored, crosslinked, pregelatinized, starch and product
AU649909B2 (en) 1992-02-07 1994-06-02 National Starch And Chemical Investment Holding Corporation Purification of polysaccharides
JPH05221838A (en) 1992-02-10 1993-08-31 Anpurein:Kk Dressing and dyeing agent for hair
US5206009A (en) * 1992-06-17 1993-04-27 Isp Investments Inc. Non-aerosol, low voc, pump hair spray composition
US5679556A (en) * 1992-12-15 1997-10-21 Shin-Etsu Chemical Co., Ltd. Process for the recovery and purification of xanthan gum
DE4315405A1 (en) * 1993-05-08 1994-11-10 Wella Ag Hair treatment products
AU7552494A (en) 1993-07-30 1995-02-28 National Starch And Chemical Investment Holding Corporation Heat treated noncohesive starches and flours and process for their production
JP3537467B2 (en) 1993-08-25 2004-06-14 花王株式会社 Hair cosmetics
JP3294393B2 (en) 1993-08-31 2002-06-24 花王株式会社 Hair cosmetics
JPH07233034A (en) 1993-12-28 1995-09-05 Kao Corp Hair fixing agent composition
EP0664113A3 (en) 1993-12-28 1996-07-10 Kao Corp Hairdressing composition.
JP3765858B2 (en) 1994-12-22 2006-04-12 サンスター株式会社 Hair treatment composition
US5593503A (en) * 1995-06-07 1997-01-14 National Starch And Chemical Investment Holding Corporation Process for producing amylase resistant granular starch
CN1129419C (en) 1996-01-22 2003-12-03 花王株式会社 Hair cosmetic composition
JPH09255534A (en) 1996-03-19 1997-09-30 Shiseido Co Ltd Hair cosmetic and its production
US6017860A (en) * 1996-04-15 2000-01-25 Stepan Company Cleaning, conditioning and styling hair care compositions
NZ314804A (en) 1996-05-23 1998-12-23 Unilever Plc Skin whitening composition containing sunscreen agent, placenta extract and xanthan gum
AU2785697A (en) 1996-06-05 1998-01-05 Rhone-Poulenc, Inc. Non-aqueous slurries of water soluble polymers
JP3524272B2 (en) * 1996-07-23 2004-05-10 伊那食品工業株式会社 Xanthan gum modification method and modified xanthan gum
US5849280A (en) 1996-08-06 1998-12-15 A-Veda Corporation Hair conditioning solid
KR20000068433A (en) 1996-09-04 2000-11-25 데이비드 엠 모이어 Personal Care Compositions
US6113881A (en) * 1996-09-20 2000-09-05 Helene Curtis, Inc. Hair styling mousse compositions comprising carboxylated polyurethane resins
US6241971B1 (en) 1997-09-25 2001-06-05 The Procter & Gamble Company Hair styling compositions comprising mineral salt, lipophilic material, and low levels of surfactant
JP4174091B2 (en) 1997-10-20 2008-10-29 日清オイリオグループ株式会社 High viscosity xanthan gum and process for producing the same
JPH11236310A (en) * 1997-12-18 1999-08-31 Kose Corp Cosmetic material
JP3597052B2 (en) 1998-08-07 2004-12-02 日清オイリオグループ株式会社 Cosmetics
JP2001181158A (en) * 1999-12-27 2001-07-03 Lion Corp Hair cosmetic
GB2363386B (en) 2000-06-16 2004-07-28 Chesham Chemicals Ltd Fluid gel comprising xanthan and non-gelling polysaccharides
US6497889B2 (en) 2000-06-20 2002-12-24 Kyowa Hakko Kogyo Co., Ltd. Cosmetics
US20030228267A1 (en) * 2001-07-09 2003-12-11 Aust Duncan T. Suncreen composition wit enhanced spf and water resistant properties
DE60221354T2 (en) * 2001-02-05 2008-04-10 Amcol International Corp., Arlington Heights MULTIFUNCTIONAL ADDITIVE COMPRISING PARTICULATE COMPONENTS FOR COSMETIC COMPOSITIONS AND METHOD FOR THE PRODUCTION THEREOF
GB2380938B (en) * 2001-08-17 2005-06-22 Nat Starch Chem Invest Use of xanthan gum as a hair fixative
US20030108505A1 (en) 2001-08-17 2003-06-12 Hongjie Cao Use of xanthan gum as a hair fixative
US20030049290A1 (en) * 2001-08-31 2003-03-13 Jha Brajesh Kumar Deodorant composition
US6531118B1 (en) * 2001-12-11 2003-03-11 Avon Products, Inc. Topical compositions with a reversible photochromic ingredient
JP4072458B2 (en) * 2003-05-14 2008-04-09 日本エヌエスシー株式会社 Aqueous composition for cosmetics and cosmetics comprising the same
CA2526536C (en) * 2003-05-29 2010-10-12 Sun Pharmaceuticals Corporation Sunscreen composition
US6887400B1 (en) * 2003-10-30 2005-05-03 Nalco Company Water-soluble polyaminoamides comprising 1,3-diimines as sunscreen agents

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3349077A (en) * 1965-05-17 1967-10-24 Kelco Co Etherified xanthomonas hydrophilic colloids and process of preparation
US4591610A (en) * 1983-03-23 1986-05-27 L'oreal Thickened or gelled composition for conditioning hair
US5198469A (en) * 1990-12-11 1993-03-30 Shigenobu Sakata Bath lotion and body lotion with pharmaceutical effect

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030143179A1 (en) * 2001-08-17 2003-07-31 Hongjie Cao Use of xanthan gum as a hair fixative
US9072683B2 (en) 2001-08-17 2015-07-07 Akzo Nobel N.V. Use of xanthan gum as a hair fixative
US8790629B2 (en) 2003-02-21 2014-07-29 Akzo Nobel N. V. High viscosity heat-treated xanthan gum
US8545828B1 (en) 2003-02-21 2013-10-01 Akzo Nobel N. V. High viscosity heat-treated xanthan gum
US8362089B2 (en) 2003-05-14 2013-01-29 Akzo Nobel N.V. Aqueous composition for cosmetics and cosmetic including the same
US20080131469A1 (en) * 2003-05-14 2008-06-05 National Starch And Chemical Inverstment Holding Corporation Aqueous composition for cosmetics and cosmetic including the same
US8431619B2 (en) 2003-05-14 2013-04-30 Akzo Nobel N.V. Aqueous composition for cosmetics and cosmetic including the same
KR101048382B1 (en) * 2004-03-15 2011-07-11 주식회사 엘지생활건강 Spray cosmetic composition that improves the durability of makeup cosmetics without stickiness
US20050255067A1 (en) * 2004-05-17 2005-11-17 Leighton John C Hair fixative film
US7972589B2 (en) 2004-05-17 2011-07-05 Akzo Nobel N.V. Hair fixative film
EP1598046A1 (en) * 2004-05-17 2005-11-23 National Starch and Chemical Investment Holding Corporation Hair fixative film
US20080085255A1 (en) * 2006-10-06 2008-04-10 L'oreal Aqueous fatty monoamine-containing anti-frizz composition for hair
EP1952842A2 (en) 2007-01-31 2008-08-06 National Starch and Chemical Investment Holding Corporation Sunscreen compositions
US20080181858A1 (en) * 2007-01-31 2008-07-31 National Starch And Chemical Investment Holding Corporation Sunscreen Compositions
US9149664B2 (en) 2007-01-31 2015-10-06 Akzo Nobel N.V. Sunscreen compositions
US20110212145A1 (en) * 2010-03-01 2011-09-01 Honeywell International Inc. Hair fixatives comprising cross linked starches
US20150136167A1 (en) * 2012-05-21 2015-05-21 Conopco, Inc., D/B/A Unilever Method of treating hair
US10588839B2 (en) 2013-11-21 2020-03-17 Conopco, Inc. Method of shaping hair
US10617615B2 (en) 2013-11-21 2020-04-14 Conopco, Inc. Method of treating hair
WO2016081465A1 (en) * 2014-11-20 2016-05-26 The Procter & Gamble Company Hair care compositions comprising dehydroxanthan gum
WO2019115706A1 (en) * 2017-12-14 2019-06-20 L'oreal Monophasic appearance cosmetic hair composition comprising a particular non-ionic surfactant
FR3075042A1 (en) * 2017-12-14 2019-06-21 L'oreal CAPILLARY COSMETIC COMPOSITION OF SINGLE-PHASE APPEARANCE COMPRISING A PARTICULAR NON-IONIC SURFACTANT
US11654093B2 (en) 2017-12-14 2023-05-23 L'oreal Monophasic appearance cosmetic hair composition comprising a particular nonionic surfactant

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