WO2013093869A2 - Composition cosmétique de type gel pour le maquillage et/ou le soin de la peau - Google Patents

Composition cosmétique de type gel pour le maquillage et/ou le soin de la peau Download PDF

Info

Publication number
WO2013093869A2
WO2013093869A2 PCT/IB2012/057588 IB2012057588W WO2013093869A2 WO 2013093869 A2 WO2013093869 A2 WO 2013093869A2 IB 2012057588 W IB2012057588 W IB 2012057588W WO 2013093869 A2 WO2013093869 A2 WO 2013093869A2
Authority
WO
WIPO (PCT)
Prior art keywords
composition
weight
phase
relative
carboxyalkyl
Prior art date
Application number
PCT/IB2012/057588
Other languages
English (en)
Other versions
WO2013093869A3 (fr
Inventor
Philippe Gabin
Patrice Styczen
Xavier Ray
Original Assignee
L'oreal
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
Application filed by L'oreal filed Critical L'oreal
Publication of WO2013093869A2 publication Critical patent/WO2013093869A2/fr
Publication of WO2013093869A3 publication Critical patent/WO2013093869A3/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/042Gels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0241Containing particulates characterized by their shape and/or structure
    • 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
    • A61K8/58Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585Organosilicon compounds
    • 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
    • A61K8/732Starch; Amylose; Amylopectin; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/895Polysiloxanes containing silicon bound to unsaturated aliphatic groups, e.g. vinyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments

Definitions

  • Gel-type cosmetic composition for making up and/or caring for the skin
  • the present invention is directed toward proposing a novel cream architecture of cosmetic composition, especially of foundation type.
  • Cosmetic compositions are commonly used to give the skin an esthetic color, but also to hide imperfections of the skin relief such as wrinkles and/or fine lines.
  • many solid or fluid, anhydrous or non-anhydrous formulations have been developed to date, namely fluids, creams, compacts, loose powders or sticks.
  • an aqueous architecture which is advantageous with regard to the fresh properties it imparts, does not ensure uniform distribution of the particulate materials within the composition.
  • makeup compositions such as foundations are generally in the form of an emulsion containing an aqueous phase and a fatty phase.
  • Each of these two phases is capable of constituting the continuous phase according to the specific needs, which gives the possibility of formulating direct emulsions (aqueous continuous phase) or inverse emulsions (fatty continuous phase).
  • aqueous continuous phase aqueous continuous phase
  • inverse emulsions fatty continuous phase
  • surfactants the water content of which is conventionally from 20% to 30%, up to 40%, rarely greater than 50% and never greater than 60%.
  • compositions that are simultaneously endowed with the freshness of aqueous formulations and the qualities of oily formulations in terms of comfort and glidance on application, and in which the combination of aqueous phase and oily phase, which is required to gain access to these qualities, also proves to be homogeneous and stabilized over time without, however, requiring the mandatory presence of surfactant.
  • the inventors have found that such an objective may be achieved provided that specific phases are combined within the same composition to form a gel-type composition.
  • the present invention relates to a gel-type cosmetic composition for making up and/or caring for the skin, comprising at least:
  • a gelled aqueous phase containing at least 3% by weight, relative to its total weight, of particles of at least one (d-C 4 ) carboxyalkyl starch and whose particle size ranges from 25 to 300 ⁇ , and
  • the oily phase has a threshold stress of greater than 1.5 Pa and preferably greater than 10 Pa.
  • the dispersed phase and the continuous phase have a threshold stress of greater than 1.5 Pa and preferably greater than 10 Pa.
  • a composition according to the invention is in the form of a creamy gel with a minimum stress below which it does not flow unless it has been subjected to an external mechanical stress.
  • Such a composition also has a certain amount of elasticity.
  • composition according to the invention may have a minimum threshold stress of 1.5 Pa and in particular greater than 10 Pa.
  • the (d-C 4 ) carboxyalkyl starch particles are in a swollen and unsplit form.
  • This swelling is the consequence of absorption of the aqueous medium by the (d-C 4 ) carboxyalkyl starch particles.
  • This swelling may be characterized by a swelling power that may be, after 24 hours of contact with the liquid to be absorbed, which is preferably aqueous, between 10 and 30 ml/g and preferably between 15 and 25 ml (volume of liquid absorbed)/g of dry particulate material. It is precisely with regard to this swelling capacity of the (d-C 4 ) carboxyalkyl starch particles that access is gained according to the invention to a gel-type architecture in the aqueous phase partly forming the composition according to the invention.
  • the composition according to the invention has a texture that becomes transformed on application. It enables the makeup result to be rendered more uniform.
  • the composition as defined above when applied to the skin, its structure breaks, leading to a pleasant fresh effect due to the release of the water or the aqueous medium present in the swollen (d-C 4 ) carboxyalkyl starch particles.
  • AMPS 2-Acrylamido-2- methylpropane sulfonic acid
  • This aqueous phase according to the invention lends itself to a homogeneous formulation that is stabilized over time with the combined oily phase to lead to a composition that is endowed with the advantages of an oil-in-water or water-in-oil emulsion and that also advantageously has a gelled, creamy appearance which is, in this respect, appealing to users.
  • the distribution of the associated particulate materials present in said composition proves to be homogeneously and durably stabilized in the gel-type architecture that is accessible according to the invention. No sedimentation or aggregation of these particles is observed.
  • the pigments are present in an individualized particulate form, i.e. not aggregated.
  • compositions according to the invention prove to be particularly advantageous with regard firstly to the sensory feeling that they give the user at the time of application, and secondly to the final makeup result obtained, which proves to be homogeneous and uniform.
  • the composition has a sufficiently thick texture to allow the user to take up the required amount in a single action.
  • the texture of the composition breaks, giving the user a sensation of freshness, due to the shear generated during its spreading on the surface of the skin.
  • the claimed compositions may be easily prepared.
  • the corresponding aqueous and oily gels may be prepared separately and then mixed together in a cold state without further requiring the obligatory presence of surfactant for achieving the expected architecture.
  • a subject of the invention is also a process for making up and/or caring for a keratin material, in particular the skin, comprising at least one step that consists in applying to said keratin material a composition in accordance with the invention.
  • composition according to the invention contains two phases, an aqueous phase and an oily phase, respectively.
  • the claimed composition is different from an emulsion.
  • An emulsion is based generally of an oily liquid phase and a water liquid phase. It is a dispersion of droplets of one of the two liquids in the other.
  • the size of the droplets forming the dispersed phase of an emulsion is typically of the order of a micrometer (0.1 to 100 microns).
  • the stability of an emulsion needs the presence of surfactant or emulsifying silicone.
  • composition according to the invention consists of a homogeneous mixture of two immiscible gels.
  • the aqueous gelified phase and the oily gelified phase interpenetrate and form by this way a stable product due to their consistency almost pasty. This consistency is achieved by a mixture of interpenetrated macro-domains.
  • the claimed composition is related to a gel-type consistency.
  • gels are diluted entangled systems with no flow when they are in the stable state. In mass, gels consist mainly of liquid. However, they behave like solids due to their entangled three-dimensional network within the liquid. These are the tangles that give to gels their structure (hardness) and contribute to their adhesion.
  • homogeneous mixture means a fine or coarse distribution of a gel to another gel uniformly dispersed in the mass.
  • the ratio between the hydrophilic gel and the lipophilic gel is determined according to the expected cosmetic properties.
  • the interpenetrating domains are not measurable objects since their size is inhomogeneous and may vary on a large scale for example from 0.1 to 1.5 mm. Accordingly, it is not possible to characterize the compositions of the invention via a size parameter.
  • the compositions according to the invention are microscopically very different from an emulsion.
  • a composition according to the invention cannot also be characterized as having a "sense", i.e. O/W or W/O sense; both gels are intertwined and are predominant in terms of their ratio in the formulation without any influence on the stability of the finished product.
  • compositions according to the invention is not smooth but only creamy or gelled and the stability of the product is sustainable without emulsifier.
  • a cosmetic composition according to the invention is preferably free of emulsifier.
  • one of its two phases acts as the continuous phase and the other is dispersed therein.
  • a composition according to the invention has an aqueous continuous phase and an oily dispersed phase.
  • a composition according to the invention has an oily continuous phase and an aqueous dispersed phase.
  • the two phases are present in a composition according to the invention in a weight ratio ranging from 95/5 to 5/95.
  • the two phases are present in a composition according to the invention in a weight ratio ranging from 75/25 to 65/35
  • the aqueous phase and the oily phase are present in a 70/30 weight ratio.
  • the aqueous phase and the oily phase are present in a 25/75 weight ratio, a 50/50 weight ratio or in a 60/40 weight ratio.
  • the dispersed phase and the continuous phase have, respectively, a threshold stress of greater than 1.5 Pa and preferably greater than 10 Pa.
  • Characterization of the threshold stresses is performed by oscillating rheology measurements. A method is proposed in the examples section of the present text.
  • RS600 imposed-stress rheometer equipped with a cone-plate measuring body (60 mm diameter) fitted with an anti-evaporation device (bell jar). For each measurement, the sample is placed delicately in position and the measurements start 5 minutes after placing the sample in the jaws (2 mm). The composition is then subjected to a stress ramp from
  • a composition according to the invention also has a certain amount of elasticity.
  • This elasticity may be characterized by a stiffness modulus G* which, under this minimum stress threshold, is at least equal to 400 Pa and preferably greater than 1000 Pa.
  • the value G* of a composition may be obtained by subjecting the composition under consideration to a stress ramp from 10 ⁇ 2 to 10 3 Pa at a set frequency of 1 Hz.
  • the aqueous phase of a composition according to the invention comprises water and optionally a water-soluble solvent.
  • water-soluble solvent denotes a compound that is liquid at room temperature and water-miscible (miscibility with water of greater than 50% by weight at 25°C and atmospheric pressure).
  • the water-soluble solvents that may be used in the composition of the invention may also be volatile.
  • the aqueous phase (water and optionally the water-miscible solvent) may be present in the composition in a content ranging from 30% to 80% by weight and preferably from 40% to 75% by weight relative to the total weight of said composition.
  • the composition of the invention is water, especially water at room temperature.
  • the aqueous phase contains from 3%) to 10%) by weight, relative to its total weight, of particles of at least one (Ci-C 4 ) carboxyalkyl starch and whose particle size ranges from 25 to 300 ⁇ .
  • the (Ci-C 4 ) carboxyalkyl starches are obtained by grafting carboxyalkyl groups onto one or more alcohol functions of starch, especially by reaction of starch and of sodium monochloroacetate in alkaline medium.
  • the carboxyalkyl groups are generally attached via an ether function, more particularly to carbon 1.
  • the degree of substitution with carboxyalkyl units of the (Ci-C 4 ) carboxyalkyl starch preferably ranges from 0.1 to 1 and more particularly from 0.15 to 0.5.
  • the degree of substitution is defined in the present invention as being the mean number of hydroxyl groups substituted with an ester or ether group per monosaccharide unit of the polysaccharide.
  • the carboxyalkyl starches are advantageously used in the form of salts and especially salts of alkali metals or alkaline-earth metals such as Na, K, Li, NH 4 , or salts of a quaternary ammonium or of an organic amine such as monoethanolamine, diethanolamine or triethanolamine.
  • the (Ci-C 4 ) carboxyalkyl starches are, in the context of the present invention, advantageously carboxymethylstarches.
  • the carboxymethylstarches preferably comprise units having the following formula:
  • X optionally covalently bonded to the carboxyl unit, denotes a hydrogen atom, an alkali metal or alkaline-earth metal such as Na, K, Li, NH 4 , a quaternary ammonium or an organic amine, for instance monoethanolamine, diethanolamine or triethanolamine.
  • X denotes an Na + cation.
  • carboxyalkyl starches that may be used according to the present invention are preferably non-pregelatinized carboxyalkyl starches.
  • carboxyalkyl starches that may be used according to the present invention are preferably partially or totally crosslinked carboxyalkyl starches.
  • a crosslinked carboxyalkyl starch has, as opposed to a non- crosslinked carboxyalkyl starch, an increased, controllable viscosity and greater stability.
  • the crosslinking thus makes it possible to reduce the syneresis and to increase the resistance of the gel to shear effects.
  • the carboxyalkyl starches under consideration according to the invention are more particularly potato carboxyalkyl starches.
  • carboxyalkyl starches that may be used according to the present invention are preferably sodium salts of carboxyalkyl starches, in particular a sodium salt of potato carboxymethyl starch, sold especially under the name Primojel by the company DMV International or Glycolys® and Glycolys LV® by the company Roquette.
  • the potato carboxymethyl starches sold especially under the name Glycolys® by the company Roquette will be used.
  • the (d-C 4 ) carboxyalkyl starch particles are present in the compositions according to the invention in a swollen and unsplit form.
  • This swelling may be characterized by a swelling power Q that may advantageously be between 10 and 30 ml/g and preferably between 15 and 25 ml (volume of liquid absorbed)/g of dry particulate material.
  • the size of the swollen carboxyalkyl starch particles used according to the present invention generally ranges from 25 to 300 ⁇ .
  • the gel Primojel containing 10% by weight of potato carboxyalkyl starch and sodium salt in water contains more than 80% of swollen particles of this starch with a diameter of greater than 50 microns and more particularly greater than 100 microns.
  • these particles are used for the preparation of the compositions according to the invention, in this swollen particulate state.
  • these particles are advantageously used in the form of an aqueous gel that is either prepared beforehand or already commercially available.
  • the gels under consideration according to the invention are advantageously translucent.
  • a carboxymethyl starch gel such as Primojel® which is at a concentration of 10% by weight may be adjusted to the required concentration before being used to prepare the expected cosmetic composition.
  • carboxyalkyl starch particles are advantageously present in a composition according to the invention in an amount adjusted to give this composition the expected properties in terms of architecture and texture.
  • the amount of (d-C 4 ) carboxyalkyl starch is advantageously adjusted to give the gel architecture thus obtained sufficient fluidity to enable easy and pleasant application to the surface of the skin.
  • these properties are present for a use of (d-C 4 ) carboxyalkyl starch particles in a proportion of less than 8% by weight, preferably less than 7% by weight and in particular from 4% to 6.5% of carboxyalkyl starch relative to the total weight of the aqueous phase.
  • the weight of the aqueous phase under consideration previously incorporates the weight of the aqueous phase plus the weight of all of the associated compounds that are soluble in this aqueous phase.
  • the aqueous phase of a composition according to the invention comprises at least one C2-C32 polyol.
  • polyol should be understood as meaning any organic molecule comprising at least two free hydroxyl groups.
  • a polyol in accordance with the present invention is present in liquid form at room temperature.
  • a polyol that is suitable for use in the invention may be a compound of linear, branched or cyclic, saturated or unsaturated alkyl type, bearing on each alkyl chain at least two -OH functions, in particular at least three -OH functions and more particularly at least four -OH functions.
  • the polyols that are advantageously suitable for formulating a composition according to the present invention are those especially containing from 2 to 32 carbon atoms and preferably 3 to 16 carbon atoms.
  • the polyol can be chosen, for example, from ethylene glycol, pentaerythritol, trimethylolpropane, propylene glycol, 1,3-propanediol, butylene glycol, isoprene glycol, pentylene glycol, hexylene glycol, glycerol, polyglycerols, such as glycerol oligomers, for example diglycerol, polyethylene glycols, and mixtures thereof.
  • said polyol is chosen from ethylene glycol, pentaerythritol, trimethylolpropane, propylene glycol, glycerol, polyglycerols, polyethylene glycols, and mixtures thereof.
  • the composition of the invention comprises at least propylene glycol.
  • composition of the invention comprises at least glycerol.
  • an oily phase comprises at least one oil.
  • oil means any fatty substance that is in liquid form at room temperature and atmospheric pressure.
  • An oily phase that is suitable for preparing the cosmetic compositions according to the invention may comprise hydrocarbon-based oils, silicone oils, fluoro oils or non- fluoro oils, or mixtures thereof.
  • the oils may be volatile or non- volatile.
  • oils of plant origin are preferred.
  • non-volatile oil means an oil with a vapor pressure of less than 0.13 Pa.
  • silicon oil is understood to mean an oil comprising at least one silicon atom, and in particular at least one Si-0 group.
  • fluoro oil means an oil comprising at least one fluorine atom.
  • hydrocarbon-based oil means an oil mainly containing hydrogen and carbon atoms.
  • the oils may optionally comprise oxygen, nitrogen, sulfur and/or phosphorus atoms, for example in the form of hydroxyl or acid radicals.
  • volatile oil means any oil that is capable of evaporating on contact with keratin materials in less than one hour, at room temperature and atmospheric pressure.
  • the volatile oil is a volatile cosmetic compound, which is liquid at room temperature, especially having a nonzero vapor pressure, at room temperature and atmospheric pressure, in particular having a vapor pressure ranging from 0.13 Pa to 40 000 Pa (10 ⁇ 3 to 300 mniHg), in particular ranging from 1.3 Pa to 13 000 Pa (0.01 to 100 mmHg) and more particularly ranging from 1.3 Pa to 1,300 Pa (0.01 to 10 mrnHg).
  • Volatile oils are volatile cosmetic compound, which is liquid at room temperature, especially having a nonzero vapor pressure, at room temperature and atmospheric pressure, in particular having a vapor pressure ranging from 0.13 Pa to 40 000 Pa (10 ⁇ 3 to 300 mniHg), in particular ranging from 1.3 Pa to 13 000 Pa (0.01 to 100 mmHg) and more particularly ranging from 1.3 Pa to 1,300 Pa (0.01
  • the volatile oils may be hydrocarbon-based oils or silicone oils.
  • volatile hydrocarbon-based oils containing from 8 to 16 carbon atoms mention may be made especially of branched Cs-Ci6 alkanes, for instance Cs-Ci6 isoalkanes (also known as isoparaffins), isododecane, isodecane, isohexadecane and, for example, the oils sold under the trade names Isopar or Permethyl, branched Cs-Ci6 esters, for instance isohexyl neopentanoate, and mixtures thereof.
  • the volatile hydrocarbon-based oil is chosen from volatile hydrocarbon-based oils containing from 8 to 16 carbon atoms, and mixtures thereof, in particular from isododecane, isodecane and isohexadecane, and is especially isohexadecane.
  • Line volatile alkanes comprising from 8 to 16 carbon atoms, in particular from 10 to 15 carbon atoms and more particularly from 11 to 13 carbon atoms, with a flash point in the range from 30 to 120°C and more particularly from 40 to 100°C.
  • the flash point is in the range from 70 to 120°C and more particularly from 80 to 100°C, and especially about 89°C.
  • the flash point is in particular measured according to standard ISO 3679.
  • a volatile linear alkane that is suitable for the invention may advantageously be of plant origin.
  • Such an alkane may be obtained, directly or in several steps, from a plant starting material such as an oil, a butter, a wax, etc.
  • a plant starting material such as an oil, a butter, a wax, etc.
  • alkanes that are suitable for use in the invention, mention may be made of the alkanes described in the patent application from the company Cognis WO 2007/068 371 , or WO 2008/155 059 (mixtures of different alkanes differing by at least one carbon).
  • linear alkanes that are suitable for use in the invention, mention may be made of n-nonane (C9), n-decane (C10), n-undecane (Cn), n-dodecane (C12), n- tridecane (C 13 ), n-tetradecane (C 14 ), n-pentadecane (C 15 ), n-hexadecane or n-hexadecane (C 16 ) and n-heptadecane (C 17 ), and mixtures thereof, and in particular mixtures of n- undecane (Cn) and n-tridecane (C 13 ) obtained in Examples 1 and 2 of patent application WO 2008/155 059 from the company Cognis, such as the mixture of n-undecane (Cn) and n-tridecane (C 13 ).
  • Volatile silicone oils that may be mentioned include linear volatile silicone oils such as hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane, tetradecamethylhexasiloxane and hexadecamethylheptasiloxane.
  • Volatile cyclic silicone oils that may be mentioned include hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane and dodecamethy Icy clo hexasilo xane .
  • Non-volatile oils include linear volatile silicone oils such as hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane, tetradecamethylhexasiloxane and hexadecamethylheptasiloxane.
  • the non- volatile oils may be chosen especially from non- volatile hydrocarbon- based, fluoro and/or silicone oils.
  • Non-volatile hydrocarbon-based oils that may especially be mentioned include: hydrocarbon-based oils of animal origin,
  • esters for instance oils of formula R 1 COOR 2 , in which Ri represents a linear or branched fatty acid residue containing from 1 to 40 carbon atoms, and R 2 represents a hydrocarbon-based chain that is especially branched, containing from 1 to 40 carbon atoms provided that Ri + R 2 ⁇ 10.
  • the esters may be chosen especially from alcohol fatty acid esters, for instance cetostearyl octanoate, isopropyl alcohol esters, such as isopropyl myristate, isopropyl palmitate, ethyl palmitate, 2-ethylhexyl palmitate, isopropyl stearate, octyl stearate, hydroxylated esters, for instance isostearyl lactate, octyl hydroxystearate, alcohol or polyalcohol ricinoleates, hexyl laurate, neopentanoic acid esters, for instance isodecyl neopentanoate, isotridecyl neopentanoate, and isononanoic acid esters, for instance isononyl isononanoate and isotridecyl isononanoate,
  • alcohol fatty acid esters for instance cetostearyl oct
  • polyol esters and pentaerythritol esters for instance dipentaerythrityl tetrahydroxystearate/tetraisostearate
  • fatty alcohols that are liquid at room temperature, with a branched and/or unsaturated carbon-based chain containing from 12 to 26 carbon atoms, for instance 2-octyldodecanol, isostearyl alcohol and oleyl alcohol,
  • C 12 -C 22 higher fatty acids such as oleic acid, linoleic acid or linolenic acid, and mixtures thereof, and
  • phenyl silicones such as phenyl trimethicones, phenyl dimethicones, phenyltrimethylsiloxydiphenylsiloxanes, diphenyl dimethicones, diphenylmethyldiphenyltrisiloxanes and 2-phenylethyl trimethylsiloxysilicates, dimethicones or phenyl trimethicone with a viscosity of less than or equal to 100 cSt, and mixtures thereof; and also mixtures of these various oils.
  • phenyl silicones such as phenyl trimethicones, phenyl dimethicones, phenyltrimethylsiloxydiphenylsiloxanes, diphenyl dimethicones, diphenylmethyldiphenyltrisiloxanes and 2-phenylethyl trimethylsiloxysilicates, dimethicones or phenyl trimethicone with a viscosity of less
  • non-volatile oil that is suitable for use in the invention, mention may be made more particularly of pentaerythrityl tetrakis(ethylhexanoate).
  • a composition according to the invention may comprise from 5% to 40% by weight and preferably from 7% to 35% by weight of oil(s) relative to the total weight of said composition.
  • an oily phase that is suitable for use in the invention may be used in the form of a mixture of pentaerythrityl tetrakis(ethylhexanoate) and isohexadecane especially in a 60/40 weight ratio.
  • the oily phase according to the invention has a threshold stress of greater than 1.5 Pa and preferably greater than 10 Pa.
  • This threshold stress value reflects a gel-type texture of this oily phase.
  • This texturing is advantageously obtained via the presence in the oily phase of at least one texturing agent.
  • this texturing agent is an organic or mineral particulate material that is capable of gelling the oil(s) with which it is combined.
  • this material is mineral and may advantageously have a BET specific surface area of greater than or equal to 300 m 2 /g, preferably greater than 500 m 2 /g and preferentially greater than 600 m 2 /g, and especially less than 1500 m 2 /g.
  • the BET specific surface area is determined according to the BET (Brunauer- Emmet-Teller) method described in the Journal of the American Chemical Society, vol. 60, page 309, February 1938, which corresponds to International Standard ISO 5794/1.
  • the BET specific surface area corresponds to the total specific surface area (thus including micropores) of the powder.
  • silica silylate powders especially those sold under the name Dow Corning VM-2270 Aerogel Fine Particles by the company Dow Corning and under the name Enova Aerogel MT 1100 by the company Cabot.
  • the oily phase of a composition according to the invention contains at least one silica silylate powder.
  • This particulate material may also be organic.
  • Non-limiting illustrations of such materials that may especially be considered are organopolysiloxane elastomers.
  • organopolysiloxane elastomer means a supple, deformable organopolysiloxane with viscoelastic properties and especially the consistency of a sponge or a supple sphere. Its modulus of elasticity is such that this material withstands deformation and has a limited ability to extend and to contract. This material is capable of regaining its original shape after stretching.
  • the organopolysiloxane elastomer may be obtained by crosslinking addition reaction of diorganopolysiloxane containing at least one hydrogen bonded to silicon and of diorganopolysiloxane containing ethylenically unsaturated groups bonded to silicon, especially in the presence of a platinum catalyst; or by dehydrogenation crosslinking condensation reaction between a diorganopolysiloxane containing hydroxyl end groups and a diorganopolysiloxane containing at least one hydrogen bonded to silicon, especially in the presence of an organotin; or by crosslinking condensation reaction of a diorganopolysiloxane containing hydroxyl end groups and of a hydrolyzable organopolysilane; or by thermal crosslinking of organopolysiloxane, especially in the presence of an organoperoxide catalyst; or by crosslinking of organopolysiloxane via high- energy radiation such as gamma rays
  • the organopolysiloxane elastomer may be obtained by reaction of dimethylpolysiloxane containing dimethylvinylsiloxy end groups and of methylhydrogenopolysiloxane containing trimethylsiloxy end groups, in the presence of a platinum catalyst.
  • the elastomer is a non-emulsifying elastomer.
  • non-emulsifying defines organopolysiloxane elastomers not containing any hydrophilic chains, and in particular not containing any polyoxyalkylene units (especially polyoxy ethylene or polyoxypropylene) or any polyglyceryl units.
  • the organopolysiloxane elastomer particles are conveyed in the form of a gel formed from an elastomeric organopolysiloxane included in at least one hydrocarbon- based oil and/or one silicone oil. In these gels, the organopolysiloxane particles are often non- spherical particles.
  • Non-emulsifying elastomers are especially described in patents EP 242 219, EP 285 886 and EP 765 656 and in patent application JP-A-61-194 009, the content of which is incorporated by way o f reference .
  • the oily phase of a composition according to the invention contains at least one organopolysiloxane elastomer and more particularly a spherical non-emulsifying organopolysiloxane elastomer.
  • the elastomer may also be an emulsifying elastomer.
  • emulsifying organopolysiloxane elastomer means an organopolysiloxane elastomer comprising at least one hydrophilic chain, such as polyoxyalkylenated organopolysiloxane elastomers and polyglycerolated silicone elastomers.
  • the emulsifying organopolysiloxane elastomer may be chosen from polyoxyalkylenated organopolysiloxane elastomers.
  • the polyoxyalkylenated organopolysiloxane elastomer is a crosslinked organopolysiloxane elastomer that may be obtained by crosslinking addition reaction of diorganopolysiloxane containing at least one hydrogen bonded to silicon and of a polyoxyalkylene containing at least two ethylenically unsaturated groups.
  • the organopolysiloxane may be obtained by reaction of polyoxyalkylene (especially polyoxyethylene and/or polyoxypropylene) with dimethylvinylsiloxy end groups and of methylhydrogenopolysiloxane with trimethylsiloxy end groups, in the presence of a platinum catalyst.
  • the polyoxyalkylenated organopolysiloxane elastomers may be formed from divinyl compounds, in particular polyoxyalkylenes containing at least two vinyl groups, which react with Si-H bonds of a polysiloxane.
  • Polyoxyalkylenated elastomers are especially described in patents US 5 236 986, US 5 412 004, US 5 837 793 and US 5 811 487, the content of which is incorporated by reference.
  • the emulsifying organopolysiloxane elastomer may also be chosen from polyglycerolated organopolysiloxane elastomers.
  • the polyglycerolated organopolysiloxane elastomer according to the invention is an organopolysiloxane elastomer that may be obtained by crosslinking addition reaction of diorganopolysiloxane containing at least one hydrogen bonded to silicon and of polyglycerolated compounds containing ethylenically unsaturated groups, especially in the presence of a platinum catalyst.
  • the polyglycerolated organopolysiloxane elastomer according to the invention is conveyed in gel form in at least one hydrocarbon-based oil and/or one silicone oil.
  • the polyglycerolated elastomer is often in the form of non-spherical particles.
  • organopolysiloxane elastomers that are suitable for use in the invention are considered provided that they are capable of gelling the oil or the mixture of oils with which they are combined.
  • non-emulsifying elastomers that are suitable for use in the invention, mention may be made especially of those sold under the names KSG-15 and KSG-16 by the company Shin-Etsu.
  • polyoxyalkylenated organopolysiloxane elastomers that are suitable for use in the invention, use may be made of those sold under the names KSG-210 and KSG-310 by the company Shin-Etsu.
  • polyglycerolated organopolysiloxane elastomers that are suitable for use in the invention, use may be made of those sold under the names KSG-710 and KSG-810 by the company Shin-Etsu.
  • the required amount of this material is liable to vary significantly according to the chemical nature and the physicochemical specificities of the material under consideration.
  • the texturing agent is a mineral material, and preferably silica silylate.
  • the silica silylate may be present in a proportion of from 0.5% to 20% by weight, preferably from 1% to 15% and especially from 2% to 10%, and preferably in a proportion of at least 6.5% by weight, relative to the total weight of the oily phase.
  • the texturing agent is an organic material, and preferably an organopolysiloxane elastomer.
  • An organopolysiloxane elastomer gel may be present in a proportion of from 40% to 100% by weight and preferably from 60% to 100% by weight, and preferably in a proportion of at least 80% by weight, relative to the total weight of the oily phase.
  • a composition according to the invention may contain other compounds conventionally considered in a cosmetic composition.
  • These compounds may be dyestuffs, fillers, waxes, pasty compounds, gums, plasticizers, gelling agents, thickeners, antioxidants, preserving agents or fragrances, and mixtures thereof.
  • a composition according to the invention also comprises at least one particulate or non-particulate, water-soluble or water-insoluble dyestuff, preferably in a proportion of at least 3% by weight relative to the total weight of the composition.
  • a composition according to the invention may contain from 3% to 15% by weight or even from 5% to 10%> by weight of dyestuff(s) relative to the total weight of the composition, taking into account, moreover, the parallel limitation imposed in terms of amount of pulverulent phase in the case of using coloring particulate materials such as pigments, which are therefore water-insoluble.
  • water-soluble dyestuf means any natural or synthetic, generally organic compound, which is soluble in an aqueous phase or water-miscible solvents and which is capable of coloring.
  • synthetic or natural water-soluble dyes for instance FDC Red 4, DC Red 6, DC Red 22, DC Red 28, DC Red 30, DC Red 33, DC Orange 4, DC Yellow 5, DC Yellow 6, DC Yellow 8, FDC Green 3, DC Green 5, FDC Blue 1, betanine (beetroot), carmine, copper chlorophylline, methylene blue, anthocyanins (enocianin, black carrot, hibiscus and elder), caramel and riboflavin.
  • the water-soluble dyes are, for example, beetroot juice and caramel.
  • the coloring particulate materials may be present in a proportion of from 0.01% to 15% by weight relative to the total weight of the composition containing them.
  • They may especially be pigments, nacres and/or particles with metallic tints.
  • pigments should be understood as meaning white or colored, mineral or organic particles that are insoluble in an aqueous solution, which are intended to color and/or opacify the composition containing them.
  • a composition according to the invention may comprise from 0.01% to 15% by weight, preferably from 0.1% to 15% by weight and better still from 1% to 15% by weight of pigments relative to the total weight of said composition.
  • the pigments may be white or colored, and mineral and/or organic.
  • mineral pigments that may be used in the invention, mention may be made of titanium oxide, titanium dioxide, zirconium oxide, zirconium dioxide, cerium oxide or cerium dioxide and also zinc oxide, iron oxide or chromium oxide, ferric blue, manganese violet, ultramarine blue and chromium hydrate, and mixtures thereof.
  • It may also be a pigment having a structure that may be, for example, of sericite/brown iron oxide/titanium dioxide/silica type.
  • Such a pigment is sold, for example, under the reference Coverleaf NS or JS by the company Chemicals and Catalysts, and has a contrast ratio in the region of 30.
  • pigments having a structure may be, for example, of silica microsphere type containing iron oxide.
  • An example of a pigment having this structure is the product sold by the company Miyoshi under the reference PC Ball PC-LL- 100 P, this pigment consisting of silica microspheres containing yellow iron oxide.
  • the pigments in accordance with the invention are iron oxides and/or titanium dioxides.
  • nacres should be understood as meaning iridescent or non- iridescent colored particles of any shape, especially produced by certain molluscs in their shell or alternatively synthesized, which have a color effect via optical interference.
  • a composition according to the invention may comprise from 0 to 15% by weight of nacres relative to the total weight of said composition.
  • the nacres may be chosen from nacreous pigments such as titanium mica coated with an iron oxide, titanium mica coated with bismuth oxychloride, titanium mica coated with chromium oxide, titanium mica coated with an organic dye and also nacreous pigments based on bismuth oxychloride. They may also be mica particles at the surface of which are superimposed at least two successive layers of metal oxides and/or of organic dyestuffs.
  • nacres examples include natural mica coated with titanium oxide, with iron oxide, with natural pigment or with bismuth oxychloride.
  • pearlescent agents available on the market, mention may be made of the pearlescent agents Timica, Flamenco and Duochrome (based on mica) sold by the company Engelhard, the Timiron pearlescent agents sold by the company Merck, the Prestige mica-based pearlescent agents sold by the company Eckart, and the Sunshine synthetic mica-based pearlescent agents sold by the company Sun Chemical.
  • the nacres may more particularly have a yellow, pink, red, bronze, orange, brown, gold and/or coppery color or glint.
  • the nacres in accordance with the invention are micas coated with titanium dioxide or with iron oxide, and also bismuth oxy chloride.
  • the term "particles with a metallic glint” means any compound whose nature, size, structure and surface finish allow it to reflect the incident light, especially in a non- iridescent manner.
  • the particles with a metallic glint that may be used in the invention are in particular chosen from:
  • - particles of at least one metal and/or of at least one metal derivative - particles comprising a single-material or multi-material organic or mineral substrate, at least partially coated with at least one layer with a metallic glint comprising at least one metal and/or at least one metal derivative;
  • metals that may be present in said particles, mention may be made, for example, of Ag, Au, Cu, Al, Ni, Sn, Mg, Cr, Mo, Ti, Zr, Pt, Va, Rb, W, Zn, Ge, Te and Se, and mixtures or alloys thereof.
  • Ag, Au, Cu, Al, Zn, Ni, Mo and Cr and mixtures or alloys thereof are preferred metals.
  • metal derivatives denotes compounds derived from metals, especially oxides, fluorides, chlorides and sulfides.
  • fillers should be understood as meaning colorless or white solid particles of any form, which are in an insoluble and dispersed form in the medium of the composition.
  • fillers of mineral or organic, natural or synthetic nature, give the composition containing them softness and give the makeup result a matt effect and uniformity.
  • mineral fillers that may be used in the compositions according to the invention, mention may be made most particularly of talc.
  • composition according to the invention may also comprise a dispersant.
  • Such a dispersant may be a surfactant, an oligomer, a polymer or a mixture of several thereof.
  • a dispersant in accordance with the invention is a surfactant.
  • a composition according to the invention comprises less than 0.1% by weight of surfactant and in particular is surfactant-free.
  • Active agent e.g., sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite, sodium metabisulfite
  • composition according to the invention may comprise at least one moisturizer (also known as a humectant).
  • the moisturizer(s) could be present in the composition in a content ranging from 0.1 % to 15% by weight, especially from 0.5% to 10% by weight or even from 1 % to 6%) by weight, relative to the total weight of said composition.
  • Humectants or moisturizers that may especially be mentioned include sorbitol, polyhydric alcohols, preferably of C 2 -Cs and more preferably of C3-C6, preferably such as glycerol, propylene glycol, 1 ,3-butylene glycol, pentylene glycol, hexylene glycol, dipropylene glycol, diethylene glycol and diglycerol, and a mixture thereof, glycerol and derivatives thereof, glycol ethers (especially containing from 3 to 16 carbon atoms) such as monopropylene, dipropylene or tripropylene glycol (Ci-C 4 )alkyl ethers, and monoethylene, diethylene or triethylene glycol (Ci-C 4 )alkyl ethers.
  • polyhydric alcohols preferably of C 2 -Cs and more preferably of C3-C6, preferably such as glycerol, propylene glycol, 1 ,3-butylene glycol, penty
  • Use will preferably be made of at least glycerol as moisturizer.
  • active agents examples that may be mentioned include vitamins and sunscreens, and mixtures thereof. It is a matter of routine operations for a person skilled in the art to adjust the nature and amount of the additives present in the compositions in accordance with the invention such that the desired cosmetic properties thereof are not thereby affected.
  • composition according to the invention has the advantage of to be prepared without the need for any heating steps by contrast to the preparation of an emulsion.
  • the method considered according to the invention may just have the need steps consisting of preparing, generally at room temperature, each phase, the aqueous gel and the oily gel, under moderate stirring.
  • the mixture of gels may be prepared at room temperature in mixers such as kneader type mixer or ribbon mixer.
  • mixers such as kneader type mixer or ribbon mixer.
  • the preparation of a composition according to the invention requires less shear.
  • a composition of the invention may advantageously be in the form of a cream foundation.
  • compositions are especially prepared according to the general knowledge of a person skilled in the art.
  • the measurements are taken using a Haake RS600 rheometer on a product at rest, at 25°C with a plate-plate rotor 0 60 mm and a 2 mm gap.
  • the measurements in the harmonic regime make it possible to characterize the viscoelastic properties of the products.
  • the technique consists in subjecting a material to a stress that varies sinusoidally over time and in measuring the response of the material to this stress.
  • the stress ( ⁇ ) and the strain ( ⁇ ) are two sinusoidal functions of time that are written in the following manner:
  • 2 ⁇ represents the angular frequency (rad.s -1 ) with N representing the frequency (Hz);
  • represents the phase angle of the stress relative to the strain (rad).
  • the two functions have the same angular frequency, but they are dephased by an angle ⁇ .
  • the behavior of the system may be assessed:
  • a complex stiffness modulus representing the overall resistance of the material to the strain, whether it is of elastic or viscous origin, is then defined by:
  • the parameter retained is the mean stiffness modulus G* recorded at the plateau measured at a frequency of 1 Hz.
  • a foundation formulation in accordance with the invention is prepared from the phases and/or compounds described below.
  • An oily gel, phase Al is prepared in a tank equipped with a "frame" paddle, using the following compounds in the weight proportions specified in the table below.
  • phase "C” is prepared in a suitable container by treatment in a three-roll mill:
  • phase "D” An aqueous solution of preserving agent below, phase "D", is prepared: Weight%
  • phase "E" The powders such as the fillers, nacres or other pulverulent additives to be considered in the foundation formulation compose phase "E".
  • This formulation is obtained by mixing together all the constituents of the composition, divided into several phases (Al , B, C, D and E), by considering a combination of phases B, D and of the glycols of phase C, which are intended for forming the aqueous gel in accordance with the invention, in the proportions described below in
  • the phases are introduced into a Clextral BC21 twin-screw extruder continuous mixer by means of volumetric pumps for the liquids and K-Tron dosers for the powders.
  • the mixing is performed at 20°C at a flow rate of 6 kg/hour and at a spin speed of 600 rpm.
  • the foundation composition is described below in Table 2.
  • Figures 1A and B show the rheological profile of the composition thus obtained.
  • composition has advantageous performance in terms of application and of makeup result. It affords an atypical texture that becomes transformed on application.
  • Example 2
  • the oily gel A2 is an organopolysiloxane elastomer sold under the name KSG- 16 by the company Shin-Etsu. It is sold as an oily mixture and is thus used in this form.
  • composition of the foundation formulation thus obtained is as follows.
  • composition has advantageous performance in terms of application and of makeup result. It affords an atypical texture that becomes transformed on application.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Cosmetics (AREA)

Abstract

La présente invention porte sur une composition cosmétique de type gel pour le maquillage et/ou le soin de la peau, comprenant au moins une phase aqueuse gélifiée contenant au moins 3 % en poids, par rapport à son poids total, de particules d'au moins un carboxy(alkyl en C1-C4)amidon et dont la taille de particule va de 25 à 300 µm et une phase huileuse gélifiée renfermant au moins un agent texturant, l'une desdites phases constituant la phase continue de ladite composition dans laquelle l'autre phase est uniformément dispersée.
PCT/IB2012/057588 2011-12-21 2012-12-21 Composition cosmétique de type gel pour le maquillage et/ou le soin de la peau WO2013093869A2 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
FR1162158 2011-12-21
FR1162158A FR2984736B1 (fr) 2011-12-21 2011-12-21 Composition cosmetique de maquillage et/ou de soin de la peau de type gel.
US201261586237P 2012-01-13 2012-01-13
US61/586,237 2012-01-13

Publications (2)

Publication Number Publication Date
WO2013093869A2 true WO2013093869A2 (fr) 2013-06-27
WO2013093869A3 WO2013093869A3 (fr) 2013-12-27

Family

ID=45992343

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2012/057588 WO2013093869A2 (fr) 2011-12-21 2012-12-21 Composition cosmétique de type gel pour le maquillage et/ou le soin de la peau

Country Status (2)

Country Link
FR (1) FR2984736B1 (fr)
WO (1) WO2013093869A2 (fr)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014167543A1 (fr) * 2013-04-12 2014-10-16 L'oreal Composition cosmétique de type gel
WO2015181733A1 (fr) * 2014-05-28 2015-12-03 L Oreal Composition cosmétique pour le maquillage et le soin de matières de kératine
WO2016030839A1 (fr) 2014-08-28 2016-03-03 L'oreal Composition gel/gel comprenant un filtre uv
WO2016030842A1 (fr) * 2014-08-28 2016-03-03 L'oreal Composition cosmétique de type gel à tenue améliorée
FR3025075A1 (fr) * 2014-08-28 2016-03-04 Oreal Nouveau dispositif de soin et/ou maquillage comprenant une composition d’architecture gel/gel
WO2018067984A1 (fr) * 2016-10-06 2018-04-12 Ken Nguyen Composition cosmétique
US10238584B2 (en) 2013-02-25 2019-03-26 L'oreal Gel-type cosmetic composition
US10398631B2 (en) 2013-02-25 2019-09-03 L'oreal Gel-type cosmetic composition
WO2020064245A1 (fr) * 2018-09-29 2020-04-02 Beiersdorf Ag Préparation cosmétique ayant des propriétés sensorielles uniques et un aspect attrayant
US20210246285A1 (en) * 2018-06-05 2021-08-12 Bio-Gate Ag Thixotropic Composition

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3025099B1 (fr) * 2014-08-28 2016-12-16 Oreal Composition cosmetique de type gel a tenue amelioree et non collante
FR3026639B1 (fr) * 2014-10-03 2018-04-13 Marlix Developpement Composition cosmetique
ES2892498T3 (es) 2015-12-17 2022-02-04 Oreal Composición de tipo gel/gel basada en pigmentos recubiertos hidrófobos y un compuesto de glicol
FR3075053B1 (fr) 2017-12-15 2020-07-10 L'oreal Composition de type gel/gel a base de pigments, d’au moins un dihydroxyalcane lineaire sature en c3-c8, d’acide salicylique sous forme libre

Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61194009A (ja) 1985-02-21 1986-08-28 Toray Silicone Co Ltd メ−クアツプ化粧料
EP0242219A2 (fr) 1986-04-17 1987-10-21 Toray Silicone Company, Ltd. Procédé pour préparer des poudres de caoutchouc silicone
EP0285886A1 (fr) 1987-04-10 1988-10-12 Ramisch Kleinewefers GmbH Procédé et installation pour le chauffage au gaz de rouleaux de calandre
JPH0517710A (ja) 1991-07-08 1993-01-26 Kansai Paint Co Ltd メタリツク塗料とその塗装法
US5236986A (en) 1991-02-27 1993-08-17 Shin-Etsu Chemical Co., Ltd. Silicone polymers and water-dispersable, pasty silicone oil compositions comprising the same
US5412004A (en) 1991-11-21 1995-05-02 Kose Corporation Silicone polymer, paste-like silicone composition, and w/o-type cosmetic composition comprising the same
JPH07258460A (ja) 1994-03-22 1995-10-09 Teijin Chem Ltd 樹脂組成物
EP0765656A1 (fr) 1995-09-29 1997-04-02 Shiseido Company Limited Composition cosmétique comprenant une émulsion eau-dans-l'huile
JPH09188830A (ja) 1996-01-05 1997-07-22 Nisshin Steel Co Ltd 高光輝性メタリック顔料
JPH10158450A (ja) 1996-11-28 1998-06-16 Shin Etsu Polymer Co Ltd 食品包装用ポリ塩化ビニル樹脂組成物
JPH10158541A (ja) 1996-11-27 1998-06-16 Nisshin Steel Co Ltd 耐候性,光輝性に優れたダークシルバー色メタリック顔料
US5811487A (en) 1996-12-16 1998-09-22 Dow Corning Corporation Thickening silicones with elastomeric silicone polyethers
US5837793A (en) 1996-03-22 1998-11-17 Dow Corning Toray Silicone Co., Ltd. Silicone rubber powder and method for the preparation thereof
WO2007068371A1 (fr) 2005-12-14 2007-06-21 Cognis Ip Management Gmbh Procede pour produire des hydrocarbures
WO2008155059A2 (fr) 2007-06-19 2008-12-24 Cognis Ip Management Gmbh Mélanges d'hydrocarbures et leur utilisation

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2806733B1 (fr) * 2000-03-21 2002-05-10 Oreal Composition sous forme d'emulsion eau-dans-huile et ses utilisations cosmetiques
FR2838335A1 (fr) * 2002-04-10 2003-10-17 Oreal Composition de mascara comprenant un polymere superabsorbant d'eau et un polymere filmogene
FR2844448B1 (fr) * 2002-09-17 2006-06-23 Lcw Les Colorants Wackherr Methode de preparation extemporanee de compositions cosmetiques ayant la texture d'une creme, et compositions pour la mise en oeuvre de cette methode
DE10343413A1 (de) * 2003-09-19 2005-04-14 Universität Hamburg Vernetzte, langzeitstabile Carboxymethylstärke als Absorptionsmittel für Wasser, deren Verwendung sowie Verfahren zu deren Herstellung
EP1694287A1 (fr) * 2003-12-01 2006-08-30 Degussa AG Preparation cosmetique a etaler, presentant une haute teneur en eau
FR2874174B1 (fr) * 2004-08-11 2006-11-24 Bourjois Soc Par Actions Simpl Composition cosmetique comprenant un polymere superabsorbant
WO2010090986A2 (fr) * 2009-02-06 2010-08-12 The Procter & Gamble Company Capsules se désintégrant contenant de l'eau

Patent Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61194009A (ja) 1985-02-21 1986-08-28 Toray Silicone Co Ltd メ−クアツプ化粧料
EP0242219A2 (fr) 1986-04-17 1987-10-21 Toray Silicone Company, Ltd. Procédé pour préparer des poudres de caoutchouc silicone
EP0285886A1 (fr) 1987-04-10 1988-10-12 Ramisch Kleinewefers GmbH Procédé et installation pour le chauffage au gaz de rouleaux de calandre
US5236986A (en) 1991-02-27 1993-08-17 Shin-Etsu Chemical Co., Ltd. Silicone polymers and water-dispersable, pasty silicone oil compositions comprising the same
JPH0517710A (ja) 1991-07-08 1993-01-26 Kansai Paint Co Ltd メタリツク塗料とその塗装法
US5412004A (en) 1991-11-21 1995-05-02 Kose Corporation Silicone polymer, paste-like silicone composition, and w/o-type cosmetic composition comprising the same
JPH07258460A (ja) 1994-03-22 1995-10-09 Teijin Chem Ltd 樹脂組成物
EP0765656A1 (fr) 1995-09-29 1997-04-02 Shiseido Company Limited Composition cosmétique comprenant une émulsion eau-dans-l'huile
JPH09188830A (ja) 1996-01-05 1997-07-22 Nisshin Steel Co Ltd 高光輝性メタリック顔料
US5837793A (en) 1996-03-22 1998-11-17 Dow Corning Toray Silicone Co., Ltd. Silicone rubber powder and method for the preparation thereof
JPH10158541A (ja) 1996-11-27 1998-06-16 Nisshin Steel Co Ltd 耐候性,光輝性に優れたダークシルバー色メタリック顔料
JPH10158450A (ja) 1996-11-28 1998-06-16 Shin Etsu Polymer Co Ltd 食品包装用ポリ塩化ビニル樹脂組成物
US5811487A (en) 1996-12-16 1998-09-22 Dow Corning Corporation Thickening silicones with elastomeric silicone polyethers
WO2007068371A1 (fr) 2005-12-14 2007-06-21 Cognis Ip Management Gmbh Procede pour produire des hydrocarbures
WO2008155059A2 (fr) 2007-06-19 2008-12-24 Cognis Ip Management Gmbh Mélanges d'hydrocarbures et leur utilisation

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 60, February 1938 (1938-02-01), pages 309

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10398631B2 (en) 2013-02-25 2019-09-03 L'oreal Gel-type cosmetic composition
US10238584B2 (en) 2013-02-25 2019-03-26 L'oreal Gel-type cosmetic composition
FR3004343A1 (fr) * 2013-04-12 2014-10-17 Oreal Composition cosmetique de type gel
WO2014167543A1 (fr) * 2013-04-12 2014-10-16 L'oreal Composition cosmétique de type gel
CN106456511A (zh) * 2014-05-28 2017-02-22 欧莱雅 用于化妆和护理角蛋白材料的美容组合物
WO2015181733A1 (fr) * 2014-05-28 2015-12-03 L Oreal Composition cosmétique pour le maquillage et le soin de matières de kératine
FR3021533A1 (fr) * 2014-05-28 2015-12-04 Oreal Composition cosmetique de type gel
CN111067807A (zh) * 2014-05-28 2020-04-28 欧莱雅 用于化妆和护理角蛋白材料的美容组合物
JP2017516782A (ja) * 2014-05-28 2017-06-22 ロレアル ケラチン物質をメイクアップ及びケアするための化粧料組成物
FR3025100A1 (fr) * 2014-08-28 2016-03-04 Oreal Composition cosmetique de type gel a tenue amelioree
CN106794135B (zh) * 2014-08-28 2020-12-22 欧莱雅 具有改善的保持力的凝胶型美容组合物
WO2016030841A3 (fr) * 2014-08-28 2016-06-30 L'oreal Nouveau dispositif de soins et/ou de maquillage comprenant une composition de type gel/architecture de gel
JP2017534308A (ja) * 2014-08-28 2017-11-24 ロレアル ゲル/ゲル構成を持つ組成物を含有する、新規な手入れおよび/またはメークアップ用デバイス
US11311465B2 (en) 2014-08-28 2022-04-26 L'oreal Gel-type cosmetic composition with improved staying power
FR3025075A1 (fr) * 2014-08-28 2016-03-04 Oreal Nouveau dispositif de soin et/ou maquillage comprenant une composition d’architecture gel/gel
CN106794135A (zh) * 2014-08-28 2017-05-31 欧莱雅 具有改善的保持力的凝胶型美容组合物
WO2016030842A1 (fr) * 2014-08-28 2016-03-03 L'oreal Composition cosmétique de type gel à tenue améliorée
WO2016030839A1 (fr) 2014-08-28 2016-03-03 L'oreal Composition gel/gel comprenant un filtre uv
CN109689013A (zh) * 2016-10-06 2019-04-26 诺赛尔股份有限公司 化妆品组合物
WO2018067984A1 (fr) * 2016-10-06 2018-04-12 Ken Nguyen Composition cosmétique
US11337899B2 (en) 2016-10-06 2022-05-24 Noxell Corporation Cosmetic composition
US20210246285A1 (en) * 2018-06-05 2021-08-12 Bio-Gate Ag Thixotropic Composition
WO2020064245A1 (fr) * 2018-09-29 2020-04-02 Beiersdorf Ag Préparation cosmétique ayant des propriétés sensorielles uniques et un aspect attrayant
CN112752561A (zh) * 2018-09-29 2021-05-04 拜尔斯道夫股份有限公司 具有独特感官特性和吸引人的外观的化妆品制剂

Also Published As

Publication number Publication date
WO2013093869A3 (fr) 2013-12-27
FR2984736B1 (fr) 2014-01-17
FR2984736A1 (fr) 2013-06-28

Similar Documents

Publication Publication Date Title
WO2013093869A2 (fr) Composition cosmétique de type gel pour le maquillage et/ou le soin de la peau
EP2958541B1 (fr) Composition cosmetique de type gel
JP5774706B2 (ja) アルキルセルロースを含む水性化粧料組成物
US8318187B2 (en) Long-wearing cosmetic compositions with improved shine
JP5567215B2 (ja) アルキルセルロースを含む水性化粧品組成物
RU2667971C2 (ru) Косметическая композиция для макияжа кожи
JP6953500B2 (ja) アルキルセルロースと、非相溶性である炭化水素およびシリコーン油とを含む組成物ならびにそれを用いる方法
EP3139900B1 (fr) Préparation d'une composition pulvérulente / pâteuse comprenant un gel d'élastomère de silicone, des particules solides et une phase liante et procédé de traitement des lèvres
KR20200081447A (ko) 셀룰로오스 입자, 질화붕소 입자 및 새틴 네이커 입자를 포함하는 윤광 새틴 효과를 갖는 조성물
WO2012085856A2 (fr) Composition cosmétique anhydre solide
WO2017023691A1 (fr) Compositions cosmétiques pour atténuer les imperfections de la peau
US20230039503A1 (en) Emulsified lip gel
WO2011001217A1 (fr) Procédé cosmétique de revêtement de matière kératinique
FR2968975A1 (fr) Composition cosmetique solide et anhydre
JP2017500350A (ja) シリコーンエラストマーと、シリコーン油と、ペースト状脂肪物質と、無極性炭化水素系化合物とを含む組成物、及び移行防止組成物としての使用
FR3117032A1 (fr) Composition gélifiée comprenant de l’aérogel de silice et de l’éthylguar comme agents épaississants
EP3565521B2 (fr) Émulsion de type h/e comprenant un alcool gras en c16 à c30, un tensioactif anionique, une huile, une cire et un solvant hydrophile
WO2011001221A1 (fr) Procédé cosmétique pour revêtir un matériau kératineux
FR3048179B1 (fr) Composition comprenant un alkylether de polysaccharide alkyle et des huiles siliconees ou fluorees incompatibles et procede la mettant en oeuvre
WO2023104924A1 (fr) Composition comprenant une combinaison d'esters de polyglycérol et d'une charge
WO2016030838A1 (fr) Gel-gel comprenant au moins deux charges avec un effet de flou
FR3045364A1 (fr) Composition comprenant de l'alkylcellulose, des huiles hydrocarbonees et siliconees incompatibles, une cire et procede la mettant en oeuvre
US20230067902A1 (en) Dilute long-wearing cosmetic composition comprising mixed sensory modifiers
KR20230110586A (ko) 적어도 하나의 지방 알코올, 비-이온성 당 에스테르, 에틸셀룰로오스를 포함하는 역상 에멀젼 및 이를 사용하는 방법
WO2011001219A1 (fr) Procédé cosmétique pour revêtir une matière kératinique

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 12823041

Country of ref document: EP

Kind code of ref document: A2

122 Ep: pct application non-entry in european phase

Ref document number: 12823041

Country of ref document: EP

Kind code of ref document: A2