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WO2013190704A1 - Composition cosmétique liquide comprenant une huile d'hydrocarbure non volatile, une huile de diméthicone non volatile et un ester de dextrine - Google Patents

Composition cosmétique liquide comprenant une huile d'hydrocarbure non volatile, une huile de diméthicone non volatile et un ester de dextrine Download PDF

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Publication number
WO2013190704A1
WO2013190704A1 PCT/JP2012/066454 JP2012066454W WO2013190704A1 WO 2013190704 A1 WO2013190704 A1 WO 2013190704A1 JP 2012066454 W JP2012066454 W JP 2012066454W WO 2013190704 A1 WO2013190704 A1 WO 2013190704A1
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WIPO (PCT)
Prior art keywords
oil
volatile
composition
weight
composition according
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PCT/JP2012/066454
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English (en)
Inventor
Momoko Shimizu
Maki Ishida
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
Priority to PCT/JP2012/066454 priority Critical patent/WO2013190704A1/fr
Priority to PCT/JP2013/067744 priority patent/WO2013191302A1/fr
Priority to JP2014560185A priority patent/JP6271448B2/ja
Publication of WO2013190704A1 publication Critical patent/WO2013190704A1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/732—Starch; Amylose; Amylopectin; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8105—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • A61K8/8111—Homopolymers or copolymers of aliphatic olefines, e.g. polyethylene, polyisobutene; Compositions of derivatives of such polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips

Definitions

  • the present invention relates to a liquid cosmetic composition, more particularly to a cosmetic composition for making up and/or caring for the skin and/or the lips, comprising at least a non-volatile dimethicone oil, a non-volatile hydrocarbonated apolar oil and a dextrin ester.
  • the present invention also relates to the processes using such composition for making up and/or caring for the skin and/or the lips, comprising the application to the skin and/or the lips of such cosmetic composition.
  • liquid compositions comprising non-volatile oils for obtaining a shiny deposit on the skin or the lips and gloss remanence.
  • the cosmetic properties of the said liquid compositions in particular the applications properties such as the glide and the easiness to apply and to obtain a uniform deposit on the lips and/or the skin, and in particular to have a deposit on the skin and / or the lips that has a good transfer resistance, and in particular a good color transfer resistance.
  • the deposit should also be sparingly tacky or not tacky and have a good shine level.
  • the aim of the present invention is to overcome these drawbacks and to propose a liquid cosmetic composition that is homogenous, stable (for example no separation into two phases, and/or exsudation, and/or sedimentation of the pigments), and capable, on the one hand, of affording good cosmetic properties; in particular applications properties such as glide and easiness to apply, in particular on the lips, good adhesion to the support (skin or lips) and thus good remanence of the deposit of the composition, in particular no or low level transfer of the color of the deposit, and forming a non-tacky or sparingly tacky deposit, having a good level of shine.
  • the invention relates to a liquid cosmetic composition for making up and/or caring for the skin and/or the lips, comprising in a physiologically acceptable medium, at least one fatty phase comprising:
  • non-volatile non-phenylated silicone oil(s) having at least a dimethicone part, or mixture thereof, relative to the total weight of the composition from 10% to 75% by total weight of non-volatile hydrocarbonated apolar oil(s), or mixture thereof, relative to the total weight of the composition, and
  • Such a composition is stable and homogenous, and are preferably makeup compositions, whose deposition on keratin materials, and in particular the lips and/or the skin, is easy to apply (good glide, homogenous deposit) and the deposit has good transfer resistance after application (in particular, no transfer or poor transfer of the color of the deposit, in particular on a cup or a glass while drinking for example).
  • the deposit obtained with such composition is sparingly tacky or non-tacky, and has a good level of shine.
  • the present invention also relates to a cosmetic process for making up and/or caring for the skin and/or the lips, comprising at least the application to the said skin and/or the said lips of a liquid composition comprising, in a physiologically acceptable medium:
  • non-volatile non-phenylated silicone oil(s) having at least a dimethicone part, or mixture thereof, relative to the total weight of the composition from 10% to 75% by weight of non- volatile hydrocarbonated apolar oil(s), relative to the total weight of the composition, and
  • the composition under consideration according to the invention is an oil-in-oil type composition.
  • the non-volatile silicone oil and the non-volatile hydrocarbon oil is in a stable oil in oil state before application, without being separated from each other. After application, the non-volatile silicone oil comes up to the surface of the deposit, and this separated non-volatile silicone oil covers an adherent layer of the non-volatile hydrocarbonated oil. Therefore, the resulting composition has good transfer resistance and offers a good level of shine. Rubbing t he lips again each other during application further enhance this separation.
  • composition under consideration according to the invention is anhydrous.
  • physiologically acceptable medium is intended to denote a medium that is suitable for the application of a composition to the skin and/or the lips, for instance the oils or organic solvents commonly used in cosmetic compositions.
  • the physiologically acceptable medium (acceptable tolerance, toxicology and feel) is generally adapted to the nature of the support onto which the composition is to be applied, and also to the form in which the composition is to be conditioned.
  • the combination under consideration according to the invention proves to be most particularly effective for affording a composition whose deposit on the skin or the lips that simultaneously has improved gloss and non transfer properties.
  • the deposit also exibit remanence over time, in particular of remanence of the colour of the deposit (no embrittlement or fragmentation of the deposit, which remains homogeneous) and satisfactory comfort properties, both on application (especially glidance, breakdown, thickness and uniformity of the deposit formed, and reduction of the tack on drying) and during wearing, namely softness, absence of a tacky sensation or of a sensation of tautness or dryness.
  • the invention also preferably relates to a liquid composition for making up and/or caring for the skin and/or the lips, comprising, in a physiologically acceptable medium, at least from 20% to 30% of nonvolatile non-phenylated silicone oil(s) having at least a dimethicone part, or mixture thereof, from 10% to 75% non-volatile hydrocarbonated apolar oil(s),or mixture thereof, from 3.2% to 15% dextrin fatty acid ester, and at least one colouring agent.
  • a physiologically acceptable medium at least from 20% to 30% of nonvolatile non-phenylated silicone oil(s) having at least a dimethicone part, or mixture thereof, from 10% to 75% non-volatile hydrocarbonated apolar oil(s),or mixture thereof, from 3.2% to 15% dextrin fatty acid ester, and at least one colouring agent.
  • compositions under consideration according to the invention and used in the processes according to the invention are in liquid form at 25°C.
  • the composition used according to the invention is anhydrous or contains less than 3% by weight of water and preferably less than 1% by weight of water, relative to the total weight of the composition.
  • anhydrous especially means that water is preferably not deliberately added to the composition, but may be present in trace amount in the various compounds used in the composition.
  • composition according to the invention and/or that used according to the process according to the invention may be in the form of a composition for making up the skin and/or the lips, especially for facial or bodily skin; it may be a complexion product such as a foundation, a face powder or an eyeshadow; a lip product such as a lipcare product; a concealer product; a blusher; an eyeliner; a lip pencil or an eye pencil; a body makeup product; a gloss (lip gloss).
  • the composition is intended for making up the lips and it is more particularly a gloss (liquid lipstick).
  • the lips compositions according to the invention are anhydrous.
  • the composition has at 25°C a viscosity of between 1 and 25 Pa.s, preferably between 2 and 20 Pa.s and preferably between 4 and 17 Pa.s.
  • the viscosity at 25°C of a composition according to the invention is between 5 and 16 Pa.s.
  • the viscosity measurement is generally performed at 25°C, using a Rheomat RM180 viscometer equipped with a No. 4 spindle the measurement being performed after 10 minutes of rotation of the spindle in the composition (after which time stabilization of the viscosity and of the spin speed of the spindle are observed), at a shear rate of 200 rpm.
  • the composition has at 25°C a viscosity of between 1 and 25 Pa.s, preferably between 2 and 20 Pa.s and preferably between 4 and 17 Pa.s.
  • the viscosity at 25°C of a composition according to the invention is between 5 and 16 Pa.s, more preferably between 5 and 15 Pa.s.
  • the present invention also covers a cosmetic process for making up and/or caring for the lips, comprising at least the application to the said lips of a composition as defined above.
  • composition according to the invention comprises at least one fatty phase and more particularly at least one liquid fatty phase.
  • composition according to the invention comprises at least one non- volatile non-phenylated silicone oil having at least a dimethicone part.
  • composition according to the invention comprise from 20% to 30% by total weight of non-volatile non-phenylated silicone oil(s) having at least a dimethicone part, or mixture thereof, relative to the total weight of the composition.
  • the composition according to the invention comprise from 22% to 28% by total weight of non-volatile non-phenylated silicone oil(s) having at least a dimethicone part, or mixture thereof, relative to the total weight of the composition.
  • a composition according to the invention for caring for and/or making up the lips and more particularly of lipstick or lipgloss type may comprise from 20% to 30% by total weight of nonvolatile non-phenylated silicone oil(s) having at least a dimethicone part, or mixture thereof, relative to the total weight of the composition.
  • a composition according to the invention for caring for and/or making up the lips and more particularly of lipstick or lipgloss type may comprise from 22% to 28% by total weight of nonvolatile non-phenylated silicone oil(s) having at least a dimethicone part, or mixture thereof, relative to the total weight of the composition.
  • oil means a water-immiscible non-aqueous compound that is liquid at room temperature (25°C) and at atmospheric pressure (760 mmHg).
  • the silicone oils that may be used according to the invention are non-volatile.
  • non-volatile silicone oils that may be used in the invention preferably have a viscosity at 25°C comprised between 9cSt and 800 000 cSt, preferably less than or equal to 600 000 cSt and preferably less than or equal to 500 000 cSt.
  • the viscosity of these silicone oils may be measured according to standard ASTM D-445.
  • non-volatile oil means an oil whose vapour pressure at room temperature and atmospheric pressure is non-zero and less than 0.02 mmHg (2.66 Pa) and better still less than 10 ' mmHg (0.13 Pa).
  • the non-volatile silicone oil that may be used in the invention may be chosen especially from silicone
  • -6 2 oils especially with a viscosity at 25°C of greater than or equal to 9 centistokes (cSt) (9 x 10 m /s) and preferably less than 800 000 cSt, preferably between 50 and 600 000 cSt and preferably between 100 and 500 000 cSt.
  • the viscosity of this silicone oil may be measured according to standard ASTM D- 445.
  • TNCI Name corresponds to polydimethylsiloxane part (chemical name).
  • the non-volatile silicone oil having at least a dimethicone part can also be called a non-volatile "dimethicone oil”.
  • non-phenylated silicone oil or “non phenyl silicone oil” means a silicon oil having no phenyl substituent.
  • these non-volatile non-phenylated silicone oils are chosen from: polydimethylsiloxanes;
  • dimethicone modified with optionally fluorinated aliphatic groups, or with functional groups such as hydroxyl, thiol and/or amine groups.
  • the non-volatile non-phenylated dimethicone oil is preferably chosen from dimethicone oils, preferably chosen from polydimethylsiloxanes and/or alkyl dimethicones, and mixture thereof.
  • the non-phenylated non-volatile dimethicone oils can be chosen from:
  • PDMSs comprising alkyl or alkoxy groups, which are pendent and/or at the end of the silicone chain, these groups each containing from 2 to 24 carbon atoms, such as
  • cetyldimethicone sold under the commercial reference ABIL WAX 9801 from Evonik Goldschmidt,
  • PDMSs comprising aliphatic and/or aromatic groups, or functional groups such as
  • polyalkylmethylsiloxanes such as cetyldimethicone sold under the commercial reference ABEL WAX 9801 from Evonik Goldschmidt, or polyalkylmethylsiloxane optionally substituted with a fluorinated group, such as polymemyltrffluoropropyldimethylsiloxanes, polyalkylmethylsiloxanes substituted with functional groups such as hydroxyl, thiol and/or amine groups,
  • polysiloxanes modified with fatty acids, fatty alcohols or polyoxyalkylenes and
  • the non-volatile non-phenylated dimethicone oil is preferably chosen from dimethicone oils, preferably chosen from polydimethylsiloxanes.
  • Such polydimethylsiloxane (having the INCI name dimethicone) may be chosen from the products commercialised under the reference MIRASIL DM 50 from Bluestar, XIAMETER PMX-200
  • the pdms has a viscosity comprised between 10 cSt and 1000 cSt, more preferably between lOOcSt and 500cSt CSt to 500CSt at 25°C.
  • the polydimethylsiloxane (having the INCI name dimethicone) are chosen from the products commercialised under the reference MIRASIL DM 50 from Bluestar XIAMETER PMX- 200 SILICONE FLUID 350CS from Dow Corning, and/ or XIAMETER PMX-200 SILICONE FLUID 100CS from Dow Corning , and their mixture.
  • the non-volatile non-phenylated dimethicone oil is linear.
  • the composition comprises a mixture of non-volatile dimethicone oils, preferably, a mixture of at least two different polydimethylsiloxanes.
  • the composition comprises a mixture of two non-volatile polydimethylsiloxanes, preferably in a weight ratio comprised between 0.5 and 2.
  • the non-phenylated linear dimethicone oil may be chosen especially from the siUcones of formula (I):
  • R ls P2, R 5 and R5 are, together or separately, an alkyl radical containing 1 to 6 carbon atoms,
  • R 3 and R4 are, together or separately, an alkyl radical containing from 1 to 6 carbon atoms, a vinyl radical, an amine radical or a hydroxyl radical,
  • X is an alkyl radical containing from 1 to 6 carbon atoms, a hydroxyl radical or an amine radical, n and p are integers chosen so as to have a fluid compound, in particular whose viscosity at 25°C is between 9 centistokes (cSt) (9 x 10 ⁇ m 2 /s) and 800000 cSt.
  • cSt centistokes
  • non-volatile non-phenylated silicone oils that may be used according to the invention, mention may be made of those for which:
  • the substituents R ⁇ to Re and X represent a methyl group
  • p and n are such that the viscosity is 500 000 cSt, such as the product sold under the name SE30 by the company General Electric, the product sold under the name AK 500000 by the company Wacker, the product sold under the name Mirasil DM 500 000 by the company Bluestar, and the product sold under the name Dow Corning 200 Fluid 500000 cSt by the company Dow Corning
  • the substituents Ri to R6 and X represent a methyl group
  • p and n are such that the viscosity is 60000 cSt, such as the product sold under the name Dow Corning 200 Fluid 60000 CS by the company Dow Corning
  • Wacker Belsil DM 60 000 by the company Wacker
  • the substituents Ri to R5 and X represent a methyl group, and p and n are such that the viscosity is 350 cSt, such as the product sold under the name Dow Corning 200 Fluid 350 CS by the company Dow Corning,
  • the substituents Ri to Re represent a methyl group
  • the group X represents a hydroxyl group
  • n and p are such that the viscosity is 700 cSt, such as the product sold under the name Baysilone Fluid T0.7 by the company Momentive.
  • composition compositions comprises a
  • polyalkylmethylsiloxanes such as cetyldimethicone sold under the commercial reference ABIL WAX 9801 from Evonik Goldschmid.
  • the composition comprises from 0.1% to 10% polyalkylmethylsiloxanes, such as cetyldimethicone.
  • the phenyl dimethicone silicone oils prove to be particularly advantageous. They can especially impart a good level of gloss to the deposit on the skin or the lips made with the composition according to the invention, without generating any tack, and enable foirning a non transfer deposit in association with the non-volatile hydrocarbonated apolar oil.
  • composition according to the invention may comprise at least one additional non-volatile silicon oil, different from said non-volatile non-phenylated silicon oil having at least a dimethicone part.
  • said additional silicone oil may be a phenyl silicon oil.
  • composition according to the invention may comprises at least one additional non-volatile silicone oil, different from said non-volatile non-phenylated silicone oil having at least a dimethicone part.
  • composition according to the invention may comprise from 0.1% to 50% by total weight of additional non-volatile silicone oil(s), or mixture thereof, relative to the total weight of the composition.
  • these additional silicone oils may chosen from non-volatile phenylated silicone oil.
  • phenylated silicone oil or "phenyl silicone oil” means a silicone oil having at least one phenyl substituent.
  • non-volatile phenylated silicone oils two types may be distinguished, according to whether or not they contain a dimethicone part.
  • the non-volatile phenylated silicone oil having at least a dimethicone part can also be called a nonvolatile "phenyl dimethicone oil”.
  • the additional non-volatile phenylated silicone oil having at least a dimethicone part may be chosen from: a) the phenyl silicone oils corresponding to the following formula (TV):
  • R ⁇ to R 10 are saturated or unsaturated, linear, cyclic or branched Ci-C 3 o hydrocarbon-based radicals,
  • n, p and q are, independently of each other, integers between 0 and 900, p is an integer between 1 and 900, with the proviso that the sum m+n+q is other than 0.
  • the sum m+n+q is between 1 and 100.
  • the sum m+n+p+q is between 1 and 900 and better still between 1 and 800.
  • q is equal to 0.
  • Ri to R 10 independently of each other, represent a saturated or unsaturated linear or branched -Qo, hydrocarbon radical, preferably saturated, and especially Q-Cn hydrocarbon-based radical, in particular C 3 -C 16 and more particularly C 4 -C 10 , or a monocyclic or polycyclic C 6 -C 14 and especially 0- 3 aryl radical, or an aralkyl radical.
  • Ri to R 10 may each represent a methyl, ethyl, propyl, butyl, isopropyl, decyl, dodecyl or octadecyl radical, or alternatively a phenyl, tolyl, benzyl or phenethyl radical.
  • R ⁇ to R 10 may especially be identical, and in addition may preferably be a methyl radical. thereof:
  • Rj R 2 , R 5 and Re independently of each other, are saturated or unsaturated, linear, cyclic or branched -C30 hydrocarbon-based radicals, preferably are a -C30 alkyl radical, an aryl radical or an aralkyl radical,
  • R 3 and Rt are independently of each other Ci-C 30 hydrocarbon-based alkyl radicals
  • p is an integer between 1 and 100
  • n and n are, independently of each other, integers between 0 and 100, with the proviso that the sum n+m is between 1 and 100.
  • Ri R 2 , R 5 and Re independently of each other, represent a saturated or unsaturated linear or branched C1-C30, hydrocarbon radical, preferably saturated, and especially Q-C 12 hydrocarbon-based radical, in particular C 3 -C 16 and more particularly C 4 -C 10 , or a monocyclic or polycyclic C 6 -C 14 and especially Q0-C13 aryl radical, or an aralkyl radical.
  • Ri R 2 , R 5 and Re may each represent a methyl, ethyl, propyl, butyl, isopropyl, decyl, dodecyl or octadecyl radical, or alternatively a phenyl, tolyl, benzyl or phenethyl radical.
  • Ri R 2 , R 5 and Re may especially be identical, and in addition may be a methyl radical.
  • Ri, R 2 , R5 and Re are, together or separately, an alkyl radical containing 1 to 6 carbon atoms
  • R3 and t are, together or separately, an alkyl radical containing from 1 to 6 carbon atoms or an aryl radical, with the proviso that at least one from R 3 and R4 is a phenyl radical
  • X is an alkyl radical containing from 1 to 6 carbon atoms, a hydroxyl radical or a vinyl radical
  • n and p being integer superior or equal to 1 , chosen so as to give the oil a weight-average molecular mass of less than 200 000 g/mol, preferably less than 150 000 g/mol and more preferably less than 100 000 g mol.
  • the weight-average molecular weight of the additional non-volatile phenyl silicone oil having at least a dimethicone part according to the invention ranges from 500 to 10 000 g/mol.
  • the additional non-volatile phenylated silicone oil having at least a dimethicone part is chosen from phenyl dimethicone oil corresponding to formula (VTI)
  • Rj to 3 ⁇ 4 , m, n and p are as defined before.
  • n and p are independently of each other, integers between 1 and 100, in formula (Vn).
  • Rl to R6 are methyl radicals.
  • the silicone oil is preferably chosen from diphenyl dimethicone such as KF-54 from Shin Etsu (400 cSt), KF54HV from Shin Etsu (5000 cSt), KF-50-300CS from Shin Etsu (300 cSt), KF-53 from Shin Etsu (175cSt), KF-50-100CS from Shin Etsu (100 cSt).
  • p is between 1 and 100 in formula (VII)
  • the sum m is between 1 and 100
  • n 0 , in formula (VII).
  • the additional non-volatile silicone oils having at least a dimethicone part are chosen from: trimethylsiloxyphenyl dimethicone (for instance Belsil PDM 1000 from the company Wacker (cf. formula (V) above)), phenyl dimethicones, phenyltrimethylsiloxydiphenylsiloxanes, diphenyl dimethicones (such as KF-54 from Shin Etsu (400 cSt), KF54HV from Shin Etsu (5000 cSt), KF-50- 300CS from Shin Etsu (300 cSt), KF-53 from Shin Etsu (175cSt), KF-50-100CS from Shin Etsu (100 cSt).
  • trimethylsiloxyphenyl dimethicone for instance Belsil PDM 1000 from the company Wacker (cf. formula (V) above
  • phenyl dimethicones for instance Belsil PDM 1000 from the company Wacker (cf. formula (
  • the additional non- volatile silicon oil is a phenyl silicone oil having at least a dimethicone part, and is preferably chosen from :
  • diphenyl dimethicone such as KF-54 from Shin Etsu (400 cSt), KF54HV from Shin Etsu (5000 cSt), KF-50-300CS from Shin Etsu (300 cSt), KF-53 from Shin Etsu (175cSt), F-50-100CS from Shin Etsu (100 cSt);
  • a composition according to the invention contains at least one additional non-volatile phenylated silicone oil having no dimethicone part.
  • phenylated silicone oil or "phenyl silicone oil” means a silicone oil having at least one phenyl substituent.
  • additional non-volatile phenylated silicone oil having no dimethicone part may be chosen from a) the phenyl silicone oils corresponding to the following formula (I):
  • the phenyl silicone oil comprises at least three phenyl groups, for example at least four, at least five or at least six. b) the phenyl silicone oils corresponding to the following formula ( ⁇ ): R R R R
  • the said organopolysiloxane comprises at least three phenyl groups, for example at least four or at least five. Mixtures of the phenyl organopolysiloxanes described previously may be used. Examples that may be mentioned include mixtures of triphenyl, tetraphenyl or pentaphenyl organopolysiloxanes.
  • Such a phenyl silicone oil is preferably trimethyl pentaphenyl trisiloxane, or Tetramethyl Tetraphenyl Trisiloxane.
  • oils are especially manufactured by Dow Corning under the reference PH-1555 HPJ or Dow Corning 555 Cosmetic Fluid (chemical name: l,3,5-trimethyl-l,l,3,5,5-pentaphenyl trisiloxane; INCI name: trimethyl pentaphenyl trisiloxane), or Tetramethyl Tetraphenyl Trisiloxane sold under the reference Dow Corning 554 Cosmetic Fluid by Dow Corning may also be used.
  • the phenyl silicone oils corresponding to formula (V') below:
  • R independently of each other, are saturated or unsaturated, linear, cyclic or branched -C30 hydrocarbon-based radicals, preferably R is a -C30 alkyl radical, an aryl radical or an aralkyl radical,
  • n and n are, independently of each other, integers between 0 and 100, with the proviso that the sum n+m is between 1 and 100.
  • R independently of each other, represent a saturated or unsaturated linear or branched C30, hydrocarbon radical, preferably saturated, and especially -C ⁇ hydrocarbon-based radical, in particular C 3 -C 16 and more particularly C 4 -C 10 , or a monocyclic or polycyclic C 6 -C 14 and especially C 10 -C 13 aryl radical, or an aralkyl radical.
  • R may each represent a methyl, ethyl, propyl, butyl, isopropyl, decyl, dodecyl or octadecyl radical, or alternatively a phenyl, tolyl, benzyl or phenethyl radical.
  • R may especially be identical, and in addition may be a methyl radical.
  • n is an integer between 0 and 100 and m is an integer between 1 and 100, with the proviso that the sum n+m is between 1 and 100, in formula (Vni).
  • R is methyl radical.
  • a phenyl silicone oil of formula (VHI) with a viscosity at 25°C of between 5 and 1500 mm /s (i.e. 5 to 1500 cSt), and preferably with a viscosity of between 5 and 1000 mm 2 /s (i.e. 5 to 1000 cSt) may be used.
  • the non-volatile phenyl silicone oil is preferably chosen from phenyl trimethicones; such as DC556 from Dow Corning (22.5 cSt), the oil diphenylsiloxy
  • phenyltrimetiiicone such as KF56 A from Shin Etsu, the oil Silbione 70663V30 from Rhone-Poulenc (28 cSt).
  • the values in parentheses represent the viscosities at 25°C.
  • the additional silicone oil is a phenyl silicone oil having no dimethicone part, preferably chosen from:
  • phenyl trimethylsiloxy trisiloxane such as DC556 from Dow Corning
  • Tetramethyl Tetraphenyl Trisiloxane such as PH- 1554 HRI or Dow Corning 554 Cosmetic Fluid from Dow Corning,
  • trimethyl pentaphenyl trisiloxane such as PH-1555 HRI or Dow Corning 555 Cosmetic Fluid from Dow Corning,
  • non-volatile silicone oils different from said non-volatile non-phenylated dimethicone oil, examples that may be mentioned include silicone oils such as:
  • non- volatile phenyl silicone oil with no dimethicone part preferably chosen from : Tetramethyl Tetraphenyl Trisiloxane (such as as PH-1554 HRI or Dow Corning 554 Cosmetic Fluid from
  • phenyl trimethicones such as the phenyl trimethicone sold under the trade name DC556 by Dow Corning
  • phenyltrimethylsiloxydiphenylsiloxanes phenyltrimethylsiloxydiphenylsiloxanes
  • trimethylpentaphenyl trisiloxane such as the product sold under the name Dow Corning PH- 1555 HRI Cosmetic fluid by Dow Corning
  • diphenylsiloxy phenyltrimethicone such as KF56 A from Shin Etsu
  • non-volatile phenyl silicone oil having at least a dimethicone part
  • composition according to the invention may contain from 0.1 % to 50% by weight, in particular from 1 % to 30% by weight and preferably from 2% to 20% by weight in total of additional nonvolatile phenylated silicone oil(s), relative to the total weight of the composition.
  • compositions according to the invention comprise no additional non-volatile phenylated silicon oil, different from said non-volatile non-phenylated dimethicone oil.
  • composition according to the invention comprises at least one non-volatile apolar hydrocarbonated oil (also called apolar "hydrocarbon-based" oil).
  • composition according to the invention comprises from 10% to 75% by total weight of non-volatile hydrocarbonated apolar oil(s), relative to the total weight of the composition.
  • apolar oil means an oil whose solubility parameter at 25°C, 6 3 ⁇ 4 is equal to 0 (J/cm 3 ) 1 2 .
  • 3 ⁇ 4 characterizes the London dispersion forces derived from the formation of dipoles induced during molecular impacts
  • 3 ⁇ 4 characterizes the specific interaction forces (such as hydrogen bonding, acid/base, donor/acceptor, etc.);
  • the parameters ⁇ ⁇ , 3 ⁇ 4, 3 ⁇ 4 and 5 a are expressed in (J/cm 3 ) 1 ⁇ 2 .
  • hydrocarbon-based oil (or “hydrocarbonated oil”, or “hydrocarbon oil”) means an oil formed essentially from, or even constituted by, carbon and hydrogen atoms, and optionally oxygen and nitrogen atoms, and not containing any silicon or fluorine atoms. It may contain alcohol, ester, ether, carboxylic acid, amine and/or amide groups.
  • oils may be of plant, mineral or synthetic origin.
  • hydrocarbon-based oil may be chosen from linear or branched hydrocarbons of mineral or synthetic origin.
  • said -volatile apolar hydrocarbon-based oil may be chosen from:
  • composition according to the invention comprises at least one non-volatile
  • hydrocarbon-based apolar oil preferably chosen from polybutenes, polyisobutenes, hydrogenated polyisobutenes, polydecenes and/or hydrogenated polydecenes, and mixtures thereof.
  • a composition according to the invention may comprise a content of non-volatile apolar
  • hydrocarbonated oil(s) ranging from 10% to 75% by total weight, preferably from 20% to 60% by total weight and preferably from 30% to 50% by weight, relative to the total weight of the composition.
  • said non-volatile apolar hydrocarbonated oil comprise at least a hydrogenated polydecene and/or hydrogenated polyisobutene, preferably in a total content ranging from 10% to 75% by total weight, preferably from 20% to 60% by total weight, relative to the total weight of the composition.
  • non-volatile hydrocarbon oil comprise at least a hydrogenated polydecene and/or hydrogenated polyisobutene, preferably in a total content ranging from from 30% to 50%> by total weight, relative to the total weight of the composition.
  • the weight ratio of the total apolar non-volatile hydrocarbonated oil(s) to the total nonvolatile non-phenylated dimethicone oil(s) is between 0,3 and 4.
  • the weight ratio of the total apolar non- volatile hydrocarbonated oil(s) to the total non-volatile non-phenylated dimethicone oil(s) is between between 0,5 and 3,5.
  • the weight ratio of the total apolar non- volatile hydrocarbonated oil(s) to the total non-volatile non-phenylated dimethicone oil(s) is between 1 and 3. More preferably, the weight ratio of the total apolar non- volatile hydrocarbonated oil(s) to the total non-volatile non-phenylated dimethicone oil(s) is between 1.5 and 2.5.
  • the weight ratio of the non-volatile apolar hydrocarbonated oil(s) to the non-volatile silicon oil(s), preferably to the non- volatile non-phenylated silicon oil(s) having at least a dimethicone part is between 0,3 and 4, preferably between 0,5 and 3,3, preferably between 1 and 3, and even more preferably between 1.5 and 2.5. More preferably, the weight ratio of the non-volatile non-phenylated silicon oil(s) to the non- volatile apolar hydrocarbonated oil(s) is between 1.5 and 2.5.
  • composition according to the invention may also comprises at least one additional compound, preferably chosen from a hydrocarbonated polar oil, and/or an additional non-volatile silicone oil, different from said non-phenylated silicon oil having at least a dimethicone part, and/or a volatile oil, and/or a fatty pasty compound, and/or a filler, and/or a colouring agent, and/or mixture thereof.
  • additional compound preferably chosen from a hydrocarbonated polar oil, and/or an additional non-volatile silicone oil, different from said non-phenylated silicon oil having at least a dimethicone part, and/or a volatile oil, and/or a fatty pasty compound, and/or a filler, and/or a colouring agent, and/or mixture thereof.
  • composition according to the invention comprises an additional non-volatile polar hydrocarbonated oil.
  • polar oil means an oil whose solubility parameter at 25°C, 5 a , is other than 0 (J/cm 3 ) 1 ⁇ .
  • oils may be of plant, mineral or synthetic origin.
  • the additional hydrocarbon-based non- volatile polar oil may be chosen from the list of oils below, and mixtures thereof:
  • hydrocarbon-based plant oils such as liquid triglycerides of fatty acids containing from 4 to
  • ester oils preferably chosen from:
  • fatty acid esters in particular of 4 to 22 carbon atoms, and especially of octanoic acid, heptanoic acid, lanolic acid, oleic acid, lauric acid or stearic acid, for instance propylene glycol dioctanoate, propylene glycol monoisostearate or neopentyl glycol diheptanoate;
  • esters for instance the oils of formula RiCOOR 2 in which Ri represents a linear or branched fatty acid residue comprising from 4 to 40 carbon atoms and R 2 represents a hydrocarbon-based chain, which is especially branched, containing from 4 to 40 carbon atoms, on condition that Rj + R 2 16, for instance purcellin oil (cetostearyl octanoate), isononyl isononanoate, C 12 to C 15 alkyl benzoate, 2-ethylhexyl palmitate, octyldodecyl neopentanoate,
  • linear fatty acid esters with a total carbon number ranging from 35 to 70 for instance pentaerythrityl tetrapelargonate (MW : 697 g/mol);
  • R 1 represents a diol dimer residue obtained by hydrogenation of dilinoleic diacid
  • R represents a hydrogenated dilinoleic diacid residue
  • h represents an integer ranging from 1 to 9
  • polyesters obtained by condensation of an unsaturated fatty acid dimer and/or trimer and of diol, such as those described in patent application FR 0 853 634, in particular such as dilinoleic acid and 1,4-butanediol. Mention may especially be made in this respect of the polymer sold by Biosynthis under the name Viscoplast 14436H (INCI name: dilinoleic acid/butanediol copolymer), or copolymers of polyols and of diacid dimers, and esters thereof, such as Hailuscent lSDA;
  • fatty alcohols containing from 12 to 26 carbon atoms which are preferably branched, for instance octyldodecanol, 2-butyloctanol, 2-hexyldecanol, 2-undecylpentadecanol and oleyl alcohol;
  • C12-C22 higher fatty acids such as oleic acid, linoleic acid and linolenic acid, and mixtures thereof;
  • oils of plant origin such as sesame oil (820.6 g/mol);
  • fatty acids containing from 12 to 26 carbon atoms for instance oleic acid
  • composition according to the invention comprises at least one additional non-volatile polar hydrocarbon oil chosen from:
  • vinylpyrrolidone copolymers preferably such as the vinylpyrrolidone/1 -hexadecene copolymer
  • hydroxylated esters preferably with a total carbon number ranging from 35 to 70, preferably chosen from polyglyceryl-2 triisostearate, isostearyl lactate, octyl hydroxystearate, octyldodecyl hydroxystearate, diisostearyl malate, glyceryl stearate; diethylene glycol diisononanoate;
  • oils from plant origin preferably chosen from liquid triglycerides of fatty acids
  • a composition according to the invention may comprise a content of additional non- volatile polar hydrocarbonated oil ranging from 1 % to 80%, for example from 2% to 70% by weight and preferably from 5% to 60% by weight, relative to the total weight of the composition.
  • a composition according to the invention may comprise a content of additional non- volatile polar hydrocarbonated oil ranging from 5% to 60% by weight, preferably from 10 to 50% by weight, relative to the total weight of the composition.
  • the weight ratio of the total non-volatile hydrocarbonated oil(s) ( ie polar and apolar oil) to the total non-volatile silicone oil(s) is between 0,3 and 10. More preferably, the weight ratio of the total non-volatile hydrocarbonated oil(s) to the total nonvolatile phenyl dimethicone oil(s) is between between 0,5 and 5.
  • the weight ratio of the total non-volatile hydrocarbonated oil(s) to the total nonvolatile phenyl dimethicone oil(s) is between 1 and 3.
  • the weight ratio of the total non-volatile hydrocarbonated oil(s) to the total nonvolatile phenyl dimethicone oil(s) is between 1.5 and 2.5.
  • a cosmetic makeup and or care composition according to the invention also comprises a cosmetically acceptable medium that may comprise the usual ingredients, as a function of the intended use of the composition.
  • the composition according to the invention may comprise, besides said non-volatile silicone oil and said non- volatile hydrocarbonated oil, an additional liquid fatty phase, preferably chosen from non-volatile polar hydrocarbonated oils described before, and/or non-volatile silicone oils, different from said non-phenylated dimethicone oils, as described before.
  • the additional liquid fatty phase may represent from 0.1 % to 80% by weight relative to the total weight of the composition.
  • composition according to the invention and or used in a composition according to the invention may comprise from 0.1% to 75% by weight of an additional liquid fatty phase relative to its total weight.
  • composition according to the invention and/or used in a composition according to the invention may comprise from 0.5% to 70% by weight of an additional liquid fatty phase relative to its total weight.
  • the composition according to the invention may comprise a volatile oil.
  • composition under consideration according to the invention may advantageously comprise one or more oils, which may be chosen especially from volatile hydrocarbon-based oils, volatile silicone oil and fluoro oils, and mixtures thereof.
  • volatile oil means an oil that is capable of evaporating on contact with keratin materials in less than one hour, at room temperature (25°C) and atmospheric pressure (760 mmHg).
  • the volatile oil is a volatile cosmetic oil, which is liquid at room temperature, especially having a non-zero vapour pressure, at room temperature and atmospheric pressure, in particular having a vapour pressure ranging from 0.13 Pa to 40000 Pa (10 "3 to 300 mmHg), preferably ranging from 1.3 Pa to 13 000 Pa (0.01 to 100 mmHg) and preferentially ranging from 1.3 Pa to 1300 Pa (0.1 to l0 mmHg).
  • the oils may be of animal, plant, mineral or synthetic origin. Volatile fluoro oil
  • fluoro oil means an oil comprising at least one fluorine atom.
  • the fluoro oils that may be used in the invention may be chosen from fluorosilicone oils, fluoro polyethers and fluorosilicones as described in document EP-A-847 752, and perfluoro compounds.
  • perfluoro compounds means compounds in which all the hydrogen atoms have been replaced with fluorine atoms.
  • the fluoro oil according to the invention is chosen from perfluoro oils.
  • perfluoro oils that may be used in the invention, mention may be made of perfluorodecalins and perfluoroperhydrophenanthrenes.
  • the fluoro oil is chosen from
  • perfluoroperhydrophenanthrenes and especially the Fiflow® products sold by the company Creations Couliv.
  • use may be made of the fluoro oil whose INCI name is
  • the composition according to the invention further comprises a volatile hydrocarbonated oil such as isododecane and/or isohexadecane.
  • Such compound is compatible with the non-volatile hydrocarbonated and silicone oil and improve the spreadability during application and the transfer resistance of the deposit.
  • hydrocarbon-based oil (or “hydrocarbonated oil”, or “hydrocarbon oil”) means an oil formed essentially from, or even constituted by, carbon and hydrogen atoms, and optionally oxygen and nitrogen atoms, and not containing any silicon or fluorine atoms. It may contain alcohol, ester, ether, carboxylic acid, amine and/or amide groups.
  • the volatile hydrocarbon-based oils may be chosen from hydrocarbon-based oils containing from 8 to 16 carbon atoms, and especially C 8 -C 16 branched alkanes (also known as isoparafBns), for instance isododecane (also called 2,2,4,4,6-pentamethylheptane), isodecane and isohexadecane, and mixture thereof.
  • hydrocarbon-based oils containing from 8 to 16 carbon atoms, and especially C 8 -C 16 branched alkanes (also known as isoparafBns), for instance isododecane (also called 2,2,4,4,6-pentamethylheptane), isodecane and isohexadecane, and mixture thereof.
  • the volatile hydrocarbon-based oil may also be a linear volatile alkane containing 7 to 17 carbon atoms, in particular 9 to 15 carbon atoms and more particularly 11 to 13 carbon atoms. Mention may be made especially of n-nonadecane, n-decane, n-undecane, n-dodecane, n-tridecane, n-tetradecane, n- pentadecane and n-hexadecane, and mixtures thereof.
  • hydrocarbon-based oil is intended to mean an oil formed essentially, or even constituted, of carbon and hydrogen atoms, and optionally of oxygen and nitrogen atoms, and containing no silicon or fluorine atoms. It may contain alcohol, ester, ether, carboxylic acid, amine and/or amide groups.
  • composition according to the invention also comprises at least isododecane and/or isohexadecane.
  • the composition is free of additional volatile hydrocarbonated oil other than isododecane and/or isohexadecane. More particularly, the composition according to the invention contains between 0.1% and 20% by weight of volatile oil, preferably isododecane and/or isohexadecane, relative to its total weight. Preferably, the composition according to the invention contains between 1 % and 15% by weight of volatile oil, preferably of isododecane and/or isohexadecane, relative to its total weight.
  • composition according to the invention contains between 1% and 10% by weight of volatile oil, preferably of isododecane and/or isohexadecane, relative to its total weight.
  • ketones which are liquid at ambient temperature, such as methyl ethyl ketone or acetone
  • short-chain esters containing from 3 to 8 carbon atoms in total
  • ethers which are liquid at ambient temperature, such as diethyl ether, dimethyl ether or dichlorodiethyl ether
  • alcohols and in particular linear or branched lower monoalcohols containing from 2 to 5 carbon atoms, for instance ethanol, isopropanol or n-propanol.
  • the volatile oil has a flash point of greater than 65°C, and better still greater than 80°C.
  • a flash point of greater than 65°C, and better still greater than 80°C.
  • the composition according to the invention comprises less than 15% and better still less than 12% by weight of volatile oil having a flash point of less than 80°C, relative to the total weight of the composition.
  • compositions according to the invention may comprise at least one volatile silicone oil.
  • silicone oil is intended to mean an oil comprising at least one silicon atom, and in particular comprising Si-0 groups.
  • the volatile silicone oil that may be used in the invention may be chosen from silicone oils especially having a viscosity ⁇ 8 centistokes (cSt) (8 x 10 m Is) and preferably greater than 0.5 cSt .
  • silicon oil is intended to mean an oil comprising at least one silicon atom, and in particular comprising Si-0 groups.
  • the volatile silicone oil that can be used in the invention may be chosen from silicone oils having a flash point ranging from 40°C to 150°C, preferably having a flash point of greater than 55°C and less than or equal to 105°C, and preferentially ranging from 65°C to 95°C.
  • the flash point is in particular measured according to ISO standard 3679.
  • the volatile silicone oil may be chosen from linear or cyclic silicone oils such as linear or cyclic polydimethylsiloxanes (PDMSs) having from 3 to 7 silicon atoms.
  • Volatile silicone oils that may more particularly be mentioned include decamethylcyclopentasiloxane sold especially under the name DC-245 by the company Dow Corning,
  • a composition according to the invention may preferably also comprise at least one solid fatty substance especially chosen from waxes and/or pasty fatty substances.
  • the composition is free of wax or contains less than 5% by weight of waxes, preferably less than 3%, relative to the total weight of the composition.
  • the composition comprises at least one wax.
  • the amount of wax(es) in the makeup and/or care composition according to the invention is between 0.5% and 30% by weight, especially from 1% to 20% by weight or even 2% to 15% by weight, relative to the total weight of the composition.
  • the presence of waxes is preferred when the composition according to the invention is solid at room temperature.
  • the composition in case a makeup composition, for instance for the lips, the composition can be a lipsticks.
  • the term "wax” means a lipophilic compound that is solid at room temperature (25°C), with a reversible solid/liquid change of state, having a melting point of greater than or equal to 30°C, which may be up to 200°C.
  • the waxes may be chosen from waxes of animal, plant, mineral or synthetic origin, and mixtures thereof.
  • a composition according to the invention may comprise at least one wax, especially a hydrocarbon-based wax.
  • the composition is free of pasty fatty substances.
  • the composition comprises at least one pasty fatty substance.
  • the amount of pasty fatty substance in the makeup and/or care composition according to the invention is between 0.5% and 60% by weight, especially from 1% to 50% by weight or even 2% to 40% by weight, relative to the total weight of the composition.
  • pasty within the meaning of the present invention, is understood to mean a lipophilic fatty compound with a reversible solid/liquid change of state exhibiting, in the solid state, an anisotropic crystalline arrangement and comprising, at a temperature of 23°C, a liquid fraction and a solid fraction.
  • pasty compound within the meaning of the invention, is understood to mean a compound having a hardness at 20°C ranging from 0.001 to 0.5 MPa, preferably from 0.002 to 0.4 MPa.
  • the hardness is measured according to a method of penetration of a probe into a sample of compound and in particular using a texture analyser (for example, the TA-XT2i from Rheo) equipped with a stainless steel cylinder with a diameter of 2 mm.
  • the hardness measurement is carried out at 20°C at the centre of 5 samples.
  • the cylinder is introduced into each sample at a pre-rate of 1 mm/s and then at a measuring rate of 0.1 mm/s, the depth of penetration being 0.3 mm.
  • the value recorded for the hardness is that of the maximum peak.
  • this pasty compound is, at a temperature of 23 °C, in the form of a liquid fraction and of a solid fraction.
  • the starting melting temperature of the pasty compound is less than 23 °C.
  • the liquid fraction of the pasty compound, measured at 23°C, represents 9 to 97% by weight of the compound.
  • This liquid fraction at 23 °C preferably represents between 15 and 85%, more preferably between 40 and 85%, by weight.
  • the liquid fraction by weight of the pasty compound at 23 °C is equal to the ratio of the enthalpy of fusion consumed at 23°C to the enthalpy of fusion of the pasty compound.
  • the enthalpy of fusion of the pasty compound is the enthalpy consumed by the compound to change from the solid state to the liquid state.
  • the pasty compound is "in the solid state” when the whole of its mass is in the crystalline solid form.
  • the pasty compound is "in the liquid state” when the whole of its mass is in the liquid form.
  • the enthalpy of fusion of the pasty compound is equal to the area under the curve of the thermogram obtained using a differential scanning calorimeter (DSC), such as the calorimeter sold under the name MDSC 2920 by TA Instrument, with a rise in temperature of 5 or 10°C per minute, according to the ISO Standard 11357-3: 1999.
  • DSC differential scanning calorimeter
  • the enthalpy of fusion of the pasty compound is the amount of energy necessary to change the compound from the solid state to the liquid state. It is expressed in J/g.
  • the enthalpy of fusion consumed at 23 °C is the amount of energy absorbed by the sample to change from the solid state to the state which it exhibits at 23°C, composed of a liquid fraction and of a solid fraction.
  • the liquid fraction of the pasty compound measured at 32°C preferably represents from 30 to 100% by weight of the compound, preferably from 80 to 100%, more preferably from 90 to 100%, by weight of the compound.
  • the temperature of the end of the melting range of the pasty compound is less than or equal to 32°C.
  • the liquid fraction of the pasty compound measured at 32°C is equal to the ratio of the enthalpy of fusion consumed at 32°C to the enthalpy of fusion of the pasty compound.
  • the enthalpy of fusion consumed at 32°C is calculated in the same way as the enthalpy of fusion consumed at 23°C.
  • the pasty compound is preferably chosen from synthetic compounds and compounds of plant origin.
  • a pasty compound may be obtained by synthesis from starting materials of plant origin. Mention may be made especially, alone or as a mixture, of:
  • the pasty fatty substance is advantageously chosen from:
  • lanolin and derivatives thereof, such as lanolin alcohol, oxyethylenated lanolins, acetylated lanolin, lanolin esters such as isopropyl lanolate, and oxypropylenated lanolins,
  • polyol ethers chosen from polyalkylene glycol pentaerythrityl ethers, fatty alcohol ethers of sugars, and mixtures thereof, polyethylene glycol pentaerythrityl ether comprising five oxyethylene (5 OE) units (CTFA name: PEG-5 Pentaerythrityl Ether), polypropylene glycol pentaerythrityl ether comprising five oxypropylene (5 OP) units (CTFA name: PEG-5 Pentaerythrityl Ether) and mixtures thereof, and more especially the mixture PEG-5
  • Pentaerythrityl Ether PPG-5 Pentaerythrityl Ether and soybean oil, sold under the name
  • esters ie pasty fatty substance comprising at least one ester function
  • liposoluble polyethers that are particularly preferred are copolymers of ethylene oxide and/or of propylene oxide with C6-C 30 long-chain alkylene oxides, more preferably such that the weight ratio of the ethylene oxide and/or of the propylene oxide to the alkylene oxides in the copolymer is from 5:95 to 70:30.
  • copolymers such that the long-chain alkylene oxides are arranged in blocks having an average molecular weight from 1000 to 10 000, for example a polyoxyethylene/polydodecyl glycol block copolymer such as the ethers of dodecanediol (22 mol) and of polyethylene glycol (45 OE) sold under the brand name Elfacos ST9 by Akzo Nobel.
  • a polyoxyethylene/polydodecyl glycol block copolymer such as the ethers of dodecanediol (22 mol) and of polyethylene glycol (45 OE) sold under the brand name Elfacos ST9 by Akzo Nobel.
  • the pasty fatty substance comprises at least one ester function.
  • ester pasty fatty substances the following are especially preferred:
  • esters of a glycerol oligomer especially diglycerol esters, in particular condensates of adipic acid and of glycerol, for which some of the hydroxyl groups of the glycerols have reacted with a mixture of fatty acids such as stearic acid, capric acid, stearic acid and isostearic acid, and 12- hydroxystearic acid, preferably such as bis-diglyceryl polyacyladipate-2 sold under the brand name Softisan 649 by the company Sasol,
  • vinyl ester homopolymers containing C 8 -C 3 o alkyl groups such as polyvinyl laurate (sold especially under the reference Mexomer PP buy the company Chimex) and arachidyl propionate sold under the brand name Waxenol 801 by Alzo,
  • fatty acid triglycerides and derivatives thereof for instance triglycerides of fatty acids, which are especially Ci 0 -C 18 , and partially or totally hydrogenated such as those sold under the reference Softisan 100 by the company Sasol,
  • non-crosslinked polyesters resulting from polycondensation between a linear or branched C 4 - C 5 o dicarboxylic acid or polycarboxylic acid and a C 2 -C 50 diol or polyol,
  • the aliphatic esters of an ester resulting from the esterification of an aliphatic hydroxycarboxylic acid ester with an aliphatic carboxylic acid comprises from 4 to 30 and preferably from 8 to 30 carbon atoms.
  • the aliphatic carboxylic acid is preferably branched.
  • the aliphatic hydroxycarboxylic acid ester is advantageously derived from a hydroxylated aliphatic carboxylic acid containing from 2 to 40 carbon atoms, preferably from 10 to 34 carbon atoms and better still from 12 to 28 carbon atoms, and from 1 to 20 hydroxyl groups, preferably from 1 to 10 hydroxyl groups and better still from 1 to 6 hydroxyl groups.
  • the aliphatic hydroxycarboxylic acid ester is chosen from:
  • esters of a diol dimer and of a diacid dimer where appropriate esterified on their free alcohol or acid function(s) with acid or alcohol radicals, especially dimer dilinoleate esters; such esters may be chosen especially from the esters having the following INCI nomenclature: bis- behenyl/isostearyl/phytosteryl dimer dilinoleyl dimer dilinoleate (commercialised under the references Plandool G and Plandool G7), phytosteryl/isostearyl/stearyl/behenyl dimer dilinoleate (Plandool H or Plandool S), and mixtures thereof,
  • mango butter such as the product sold under the reference Lipex 203 by the company
  • shea butter in particular the product whose INCI name is Butyrospermum p rkii Butter, such as the product sold under the reference Sheasoft® by the company Aarhuskarlshamn, hydrogenated rosinate esters, such as dilinoleyl dimers of hydrogenated rosinate (Lusplan DD- DHR or DD-DHR from Nippon Fine Chemical); and
  • the pasty fatty substance is a hydrocarbon-based compound comprising at least one ester function.
  • the pasty fatty substance is chosen from hydrogenated castor oil isostearate (SALACOS HCIS (V -L) Big par NISSHIN OIL), bis-behenyl/isostearyl/phytosteryl dimer dilinoleyl dimer dilinoleate, bis-diglyceryl polyacyladipate-2, hydrogenated castor oil dimer dilinoleate (Risocast-DA- L®, Risocast DA-H®, sold by Kokyu Alcohol Kogyo), polyvinyl laurate, mango butter, shea butter, hydrogenated soybean oil, hydrogenated coconut oil and hydrogenated rape seed oil, and mixtures thereof.
  • SALACOS HCIS V -L
  • NISSHIN OIL hydrogenated castor oil isostearate
  • a makeup and/or care composition according to the invention may also comprise one or more fillers). According to a first embodiment, the composition is free of fillers.
  • the composition comprises at least one or more filler(s).
  • fillers should be understood as meaning colorless or white, mineral or synthetic particles of any shape, which are insoluble in the medium of the composition, irrespective of the temperature at which the composition is manufactured. These fillers serve especially to modify the rheology or the texture of the composition.
  • the fillers may be mineral or organic and of any shape, platelet-shaped, spherical or oblong, irrespective of the crystallographic form (for example lamellar, cubic, hexagonal, orthorhombic, etc.).
  • talc Mention may be made of talc, mica, silica, kaolin, clay, bentone, fumed silica particles, optionally hydrophilic- or hydrophobic-treated, polyamide (Nylon®) powder (Orgasol® from Atochem), poly- ⁇ - alanine powder and polyethylene powder, tetrafluoroethylene polymer (Teflon®) powder, lauroyllysine, starch, boron nitride, hollow polymer microspheres such as polyvinylidene
  • chloride/acrylonitrile microspheres for instance Expancel® (Nobel Industrie), acrylic acid copolymer microspheres (Polytrap® from the company Dow Corning) and silicone resin microbeads (for example Tospearls® from Toshiba), precipitated calcium carbonate, magnesium carbonate, magnesium hydrogen carbonate, hydroxyapatite, hollow silica microspheres (Silica Beads® from Maprecos), elastomeric polyorganosiloxane particles, glass or ceramic microcapsules, and metal soaps derived from organic carboxylic acids containing from 8 to 22 carbon atoms and preferably from 12 to 18 carbon atoms, for example zinc stearate, magnesium stearate, lithium stearate, zinc laurate or magnesium myristate, and mixtures thereof.
  • organic carboxylic acids containing from 8 to 22 carbon atoms and preferably from 12 to 18 carbon atoms, for example zinc stearate, magnesium stearate, lithium stearate, zinc laur
  • the composition according to the invention comprises at least silica, preferably hydrophobic treated silica.
  • the composition comprises at least one filler, and in particular chosen from fumed silicas that have optionally been hydrophilic- or hydrophobic-treated, preferably hydrophobic-treated.
  • the composition comprises at least one filler known as Silica
  • the hydrophobic groups may especially be dimethylsilyloxyl or polydimethylsiloxane groups, which are especially obtained by treating fumed silica in the presence of polydimethylsiloxane or
  • the composition according to the invention is free of "nanosilica", preferably free of hydrophobic treated silica of INCI name Silica Dimethyl Silylate.
  • nanonosilica means silica having a nanometric size, or a least a fraction of nanometric size.
  • the composition contains between 0.01% and 25% by weight and in particular between 0.1% and 20% by weight of fillers relative to the total weight of the composition.
  • the composition when in liquid form, it comprises at least one filler, preferably chosen from silica, kaolin, bentone, fumed silica particles, which have preferably been hydrophobic-treated, lauroyllysine and starch.
  • filler preferably chosen from silica, kaolin, bentone, fumed silica particles, which have preferably been hydrophobic-treated, lauroyllysine and starch.
  • composition according to the invention may comprise a filler chosen from:
  • organomodified clays which are preferably clays treated with compounds chosen especially from quaternary amines and tertiary amines.
  • Organomodified clays that may be mentioned include organomodified bentonites, such as the product sold under the name Bentone 34 by the company Rheox, and organomodified hectorites such as the products sold under the names
  • hydrophobic fumed silica Such silicas are sold, for example, under the references Aerosil R812® by the company Degussa and Cab-O-Sil TS-530® by the company Cabot, and under the references Aerosil R972® and Aerosil R974® by the company Degussa and Cab-O-Sil TS-610® and Cab-O-Sil TS-720® by the company Cabot.
  • the filler may be present in a content ranging from 0.1 % to 5% by weight and better still from 0.4% to 3% by weight relative to the total weight of the composition.
  • Hydrophobic silica aerogel particles may be present in a content ranging from 0.1 % to 5% by weight and better still from 0.4% to 3% by weight relative to the total weight of the composition.
  • the composition comprise may comprised at least hydrophobic silica aerogel particles.
  • Such compound is a filler.
  • such compound is present when the composition is free of nanosilica and more particularly free of Silica Dimethyl Silylate.
  • the hydrophobic silica aerogel particles may be present in a content ranging from 0.1 % to 15% by weight and better still from 0.1 % to 10% by weight, relative to the total weight of the composition.
  • the hydrophobic silica aerogel particles may be present in a content ranging from 0.1 % to 6% by weight and better still from 0.2% to 4% by weight, relative to the total weight of the composition.
  • the composition may comprise at least a additional filler, such as those described before for example.
  • the composition according to the invention comprises at least Hydrophobic silica aerogel particles, when the composition is free of nanometric silica particules as described before, such as Silica Dimethyl Silylate.
  • Silica aerogels are porous materials obtained by replacing (by drying) the liquid component of a silica gel with air.
  • sol-gel processes are generally synthesized via a sol-gel process in liquid medium and then dried, usually by extraction of a supercritical fluid, the one most commonly used being supercritical C0 2 . This type of drying makes it possible to avoid shrinkage of the pores and of the material.
  • the sol-gel process and the various drying processes are described in detail in Brinker CJ., and Scherer G.W., Sol-Gel Science: New York: Academic Press, 1990.
  • the hydrophobic silica aerogel particles that may be used in the present invention have a specific surface area per unit of mass (SM) ranging from 500 to 1500 m /g, preferably from 600 to 1200 m /g and better still from 600 to 800 m /g, and a size expressed as the mean volume diameter (D[0.5]), ranging from 1 to 1500 ⁇ , better still from 1 to 1000 ⁇ , preferably from 1 to 100 ⁇ , in particular from 1 to 30 ⁇ , more preferably from 5 to 25 ⁇ , better still from 5 to 20 ⁇ and even better still from 5 to 15 ⁇ .
  • SM surface area per unit of mass
  • the hydrophobic silica aerogel particles that may be used in the present invention have a size expressed as the mean volume diameter (D[0.5]) ranging from 1 to 30 ⁇ , preferably from 5 to 25 ⁇ , better still from 5 to 20 ⁇ and even better still from 5 to 15 ⁇ .
  • the specific surface area per unit of mass may be determined via the BET (Brunauer-Emmett-Teller) nitrogen absorption method described in the Journal of the American Chemical Society, vol. 60, page 309, February 1938 and corresponding to the intemational standard ISO 5794/1 (appendix D).
  • the BET specific surface area corresponds to the total specific surface area of the particles under consideration.
  • the size of the hydrophobic silica aerogel particles may be measured by static light scattering using a commercial granulometer such as the MasterSizer 2000 machine from Malvern.
  • the data are processed on the basis of the Mie scattering theory.
  • This theory which is exact for isotropic particles, makes it possible to determine, in the case of non-spherical particles, an "effective" particle diameter. This theory is especially described in the publication by Van de Hulst, H.C., "Light Scattering by Small Particles," Chapters 9 and 10, Wiley, New York, 1957.
  • the hydrophobic silica aerogel particles used in the present invention have a specific surface area per unit of mass (SM) ranging from 600 to 800 m /g and a size expressed as the mean volume diameter (D[0.5]) ranging from 5 to 20 ⁇ and better still from 5 to 15 ⁇ .
  • SM surface area per unit of mass
  • D[0.5] mean volume diameter
  • the hydrophobic silica aerogel particles used in the present invention may advantageously have a tamped density p ranging from 0.04 g/cm 3 to 0.10 g/cm 3 and preferably from 0.05 g/cm 3 to 0.08 g/cm 3 .
  • this density may be assessed according to the following protocol: 40 g of powder are poured into a measuring cylinder; the measuring cylinder is then placed on a Stav 2003 machine from Stampf Volumeter; the measuring cylinder is then subjected to a series of 2500 packing motions (this operation is repeated until the difference in volume between two consecutive tests is less than 2%); the final volume Vf of packed powder is then measured directly on the measuring cylinder.
  • the tamped density is determined by the ratio m/V f, in this instance 40/V f (Vf being expressed in cm and m in g).
  • the hydrophobic silica aerogel particles that may be used in the present invention have a specific surface area per unit of volume Sv ranging from 5 to 60 m /cm , preferably from 10 to 50 m /cm and better still from 15 to 40 m /cm .
  • Sv SM-', where p is the tamped density expressed in g cm and SMIS the specific surface area per unit of mass expressed in m /g, as defined above.
  • the hydrophobic silica aerogel particles according to the invention have an oil-absorbing capacity, measured at the wet point, ranging from 5 to 18 ml/g, preferably from 6 to 15 ml/g and better still from 8 to 12 ml g.
  • the oil-absorbing capacity measured at the wet point, noted Wp corresponds to the amount of water that needs to be added to 100 g of particle in order to obtain a homogeneous paste.
  • the oil uptake corresponds to the ratio Vs/m.
  • hydrophobic silica aerogel particles that may be used according to the present invention are preferably of silylated silica type (INCI name: silica silylate).
  • hydrophobic silica means any silica whose surface is treated with silylating agents, for example halogenated silanes such as alkylchlorosilanes, siloxanes, in particular dimethylsiloxanes such as hexamethyldisiloxane, or silazanes, so as to functionalize the OH groups with silyl groups Si-Rn, for example trimethylsilyl groups.
  • silylating agents for example halogenated silanes such as alkylchlorosilanes, siloxanes, in particular dimethylsiloxanes such as hexamethyldisiloxane, or silazanes, so as to functionalize the OH groups with silyl groups Si-Rn, for example trimethylsilyl groups.
  • hydrophobic silica aerogel particles that may be used in the invention, examples that may be mentioned include the aerogel sold under the name VM-2260 (INCI name: Silica silylate), by the company Dow Corning, the particles of which have a mean size of about 1000 microns and a specific surface area per unit of mass ranging from 600 to 800 m /g.
  • Aerogel TLD 201 Mention may also be made of the aerogels sold by the company Cabot under the references Aerogel TLD 201, Aerogel OGD 201, Aerogel TLD 203, and ENOVA AEROGEL MT 1100.
  • aerogel sold under the name VM-2270 (INCI name: Silica silylate), by the company Dow Corning, the particles of which have a mean size ranging from 5-15 microns and a specific surface area per unit of mass ranging from 600 to 800 m 2 /g (oil uptake equal to 1080 ml/100 g).
  • VM-2270 INCI name: Silica silylate
  • Dow Corning the particles of which have a mean size ranging from 5-15 microns and a specific surface area per unit of mass ranging from 600 to 800 m 2 /g (oil uptake equal to 1080 ml/100 g).
  • the hollow particles in accordance with the invention are at least partly formed from hydrophobic silica aerogel particles, preferably those with a specific surface area per unit of mass (SM)
  • D[0.5] mean volume diameter
  • hydrophobic silica aerogel particles also advantageously makes it possible to improve the stability of the composition.
  • composition according to the invention comprise from 3.2% to 15% by weight of ester of dextrin, relative to the total weight of the composition, preferably an ester of dextrin and a fatty acid, preferably a C 12 -C 24 fatty acid.
  • the dextrin ester is an ester of dextrine and a C 14 -C 18 fatty acid.
  • the dextrin ester is dextrine palmitate, for example such as those commercialised under the references Rheopearl TL ® or Rheopearl KL ® by the society CHIBA FLOUR.
  • a composition according to the invention may comprise a content of dextrin ester ranging from 3.2% to 10% by weight, preferably from 3,5 to 10% by weight, relative to the total weight of the composition.
  • a composition according to the invention may comprise a content of dextrin ester ranging from 3.5% to 8% by weight and preferably from 6% to 8% by weight, relative to the total weight of the composition.
  • compositions according to the invention may preferably comprise at least one dyestuff (also known as a colouring agent), which may be chosen from water-soluble or liposoluble dyes, pigments and nacres, and mixtures thereof.
  • dyestuff also known as a colouring agent
  • composition according to the invention may also comprise one or more dyestuffs chosen from water-soluble dyes and pulverulent dyestuffs, for instance pigments, nacres and glitter flakes that are well known to those skilled in the art.
  • the dyestuffs may be present in the composition in a content ranging from 0.01 % to 30% by weight, relative to the weight of the composition, preferably from 0.1% to 20% by weight.
  • pigments should be understood as meaning white or coloured, mineral or organic particles that are insoluble in an aqueous solution, which are intended to colour and/or opacify the resulting film.
  • the pigments may be present in a proportion of from 0.01% to 30% by weight, especially from 0.1% to 25% by weight and in particular from 0.2% to 15% by weight relative to the total weight of the cosmetic composition.
  • mineral pigments that may be used in the invention, mention may be made of titanium oxide, zirconium oxide or cerium oxide, and also zinc oxide, iron oxide or chromium oxide, ferric blue, manganese violet, ultramarine blue and chromium hydrate.
  • 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.
  • the dyestuff may also comprise a pigment with a structure that may be, for example, of silica microsphere type containing iron oxide.
  • 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.
  • DPP diketopyrrolopyrroles
  • nacres should be understood as meaning coloured particles of any form, which may or may not be iridescent, especially produced by certain molluscs in their shell, or alternatively synthesized, and which have a colour effect via optical interference.
  • the nacres may be chosen from nacreous pigments such as titanium mica coated with an iron oxide, 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 superposed 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.
  • nacres available on the market mention may be made of the nacres Timica, Flamenco and Duochrome (based on mica) sold by the company Engelhard, the Tirniron nacres sold by the company Merck, the Prestige mica-based nacres, sold by the company Eckart, and the Sunshine synthetic mica- based nacres, sold by the company Sun Chemical.
  • the nacres may more particularly have a yellow, pink, red, bronze, orange, brown, gold and/or coppery colour or tint.
  • nacres that may be used in the context of the present invention, mention may be made especially of the gold-coloured nacres sold especially by the company Engelhard under the name Brilliant gold 212G (Timica), Gold 222C (Cloisonne), Sparkle gold (Timica), Gold 4504 (Chromalite) and Monarch gold 233X (Cloisonne); the bronze nacres sold especially by the company Merck under the name Bronze fine (17384) (Colorona) and Bronze (17353) (Colorona) and by the company Engelhard under the name Super bronze (Cloisonne); the orange nacres sold especially by the company Engelhard under the name Orange 363C (Cloisonne) and Orange MCR 101 (Cosmica) and by the company Merck under the name Passion orange (Colorona) and Matte orange (17449)
  • the cosmetic composition according to the invention may also comprise water-soluble or liposoluble dyes.
  • the liposoluble dyes are, for example, Sudan red, DC Red 17, DC Green 6, ⁇ -carotene, Sudan brown, DC Yellow 11 , DC Violet 2, DC Orange 5 and quinoline yellow.
  • the water-soluble dyes are, for example, beetroot juice or methylene blue.
  • the cosmetic composition according to the invention may also contain at least one material with a specific optical effect as dyestuff.
  • This effect is different from a simple conventional hue effect, i.e. a unified and stabilized effect as produced by standard dyestuffs, for instance monochromatic pigments.
  • stabilized means lacking an effect of variability of the colour as a function of the angle of observation or alternatively in response to a temperature change.
  • this material may be chosen from particles with a metallic tint, goniochromatic coloring agents, diffracting pigments, thermochromic agents, optical brighteners, and also fibres, especially interference fibres. Needless to say, these various materials may be combined so as to afford the simultaneous manifestation of two effects, or even of a novel effect in accordance with the invention.
  • a composition according to the invention may also comprise an aqueous phase, which may represent 0.01% to 50% by weight, especially 0.1% to 30% by weight or even 1% to 20% by weight relative to the total weight of the composition.
  • This aqueous phase may be formed essentially from water, or may comprise a mixture of water and of water-miscible solvent (miscibility in water of greater than 50% by weight at 25°C) chosen especially from monoalcohols containing 1 to 5 carbon atoms such as ethanol, isopropanol, glycols containing 2 to 8 carbon atoms such as propylene glycol, ethylene glycol, 1,3- butylene glycol, dipropylene glycol, C 3 -C 4 ketones and C 2 -C 4 aldehydes, and mixtures thereof.
  • compositions according to the invention are anhydrous.
  • anhydrous especially means that water is preferably not deliberately added to the compositions, but may be present in trace amounts in the various compounds used in the compositions.
  • a makeup and/or care composition according to the invention may also comprise at least one agent usually used in cosmetics, chosen, for example, from reducing agents, thickeners, film-forming agents that are especially hydrophobic, silicone elastomers, softeners, antifoams, moisturizers, UV-screening agents, ceramides; cosmetic active agents; peptizers, fragrances, proteins, vitamins, propellants, hydrophilic or lipophilic, film-forming or non-film-foirning polymers; lipophilic or hydrophilic gelling agents.
  • the above additives are generally present in an amount for each of them of between 0.01% and 10% by weight relative to the total weight of the composition. Needless to say, a person skilled in the art will take care to select the constituents of the composition such that the advantageous properties associated with the invention are not, or are not substantially, adversely affected.
  • a composition used according to the invention may also comprise any usual cosmetic ingredient, which may be chosen especially from antioxidants, film-forming polymers, fragrances, preserving agents, emollients, moisturizers, neutralizers, sunscreens, sweeteners, vitamins, free-radical scavengers and sequestrants, and mixtures thereof.
  • the amounts of each of these various ingredients are those conventionally used in the fields under consideration, and range, for example, from 0.01% to 10% by weight relative to the total weight of the composition.
  • a composition in accordance with the invention is in liquid form at room temperature.
  • a composition according to the invention may constitute a gloss for the lips, a body makeup product, a facial or body care product or an antisun product.
  • compositions according to the invention are homogeneous and stable and gives access to a deposit on the skin or the lips that has good cosmetic properties, in particular in terms of gloss, comfort (thickness deposit) and absence of transfer of the deposit.
  • compositions according to the invention enable forming a deposit exhibits no color transfer, in particular on a cup while clrinking for a lip product, and when the composition contains one or more colouring agent(s).
  • a composition according to the invention is "stable", in particular no phase separation, and no sedimentation of the pigments and/or the nacres after 24hous at room temperature and at 50°C. More preferably, the composition according to the invention remains stable after seven days at 50°C.
  • the percentages are weight percentages and the ranges of values given in the form "between... and" include the stated lower and upper limits.
  • composition 1 illustrates invention.
  • Compositions 2 to 5 are comparative compositions not belonging to the invention.
  • compositions were obtained according to the following protocol:
  • the fillers, pigments and/or active agents of the fatty phase were ground in a three-roll mill in part of the oily phase (diisostearyl malate).
  • the rest of the liposoluble ingredients were then mixed in the heating pan at a temperature of about 100°C with Rayneri blending until a homogeneous mixture was obtained.
  • the ground pigmentary material was then incorporated into the mixture, along with the nacres, if present, and stirring was continued until the mixture was homogeneous.
  • the viscosity of the compositions at 25°C was evaluated according to the protocol described previously.
  • the compositions obtained were placed for 72 hours at 24°C and at 47°C in order to evaluate the stability of the composition. More particularly, it is observed if the composition is stable, ie remain homogenous (no phase separation and/or no sedimentation of the pigments).
  • compositions were then applied to the lips in order to evaluate the application properties and the characteristics of the deposit obtained (Shine, Color Transfer resistance, and tack).
  • the tacky nature of a deposit made on the lips with the compositions to be evaluated was evaluated 5 minutes after application by rubbing the upper and the lower lips together and the tack was assessed by the person on removal of her upper and lower lips.
  • the color transfer resistance is evaluated by applying the lips on a white cup as while drinking 5 minutes after applying the composition on the lips.
  • Formula 1 according to the invention that comprises 24 % non-volatile dimethicone oil has good application properties (smooth and good glide) and has a good color transfer resistance (almost no colour on the cup).
  • the deposit made with Formula 1 is sparingly tacky and has a good level of shine.
  • the deposits made with the comparatives compositions 2 to 4 comprising no non- volatile dimethicone, but comprising 24% of non-volatile phenyl dimethicone oils have not a good color transfer resistance.

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Abstract

La présente invention porte sur des compositions liquides pour le maquillage et/ou le soin de la peau et/ou des lèvres, comprenant un poids total de 20 % à 30 % d'une ou plusieurs huiles de silicone non phénylées non volatiles ayant au moins une partie diméthicone, ou d'un mélange de celles-ci, par rapport au poids total de la composition ; un poids de 10 % à 75 % d'une ou plusieurs huiles d'hydrocarbure apolaires non volatiles, par rapport au poids total de la composition ; et de 3,2 % à 15 % en poids d'ester de dextrine, par rapport au poids total de la composition.
PCT/JP2012/066454 2012-06-21 2012-06-21 Composition cosmétique liquide comprenant une huile d'hydrocarbure non volatile, une huile de diméthicone non volatile et un ester de dextrine WO2013190704A1 (fr)

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PCT/JP2012/066454 WO2013190704A1 (fr) 2012-06-21 2012-06-21 Composition cosmétique liquide comprenant une huile d'hydrocarbure non volatile, une huile de diméthicone non volatile et un ester de dextrine
PCT/JP2013/067744 WO2013191302A1 (fr) 2012-06-21 2013-06-21 Composition cosmétique liquide comprenant une huile hydrocarbonée non volatile, une huile de diméthicone non volatile et un ester de dextrine
JP2014560185A JP6271448B2 (ja) 2012-06-21 2013-06-21 不揮発性炭化水素化油、不揮発性ジメチコン油及びデキストリンエステルを含む液体化粧用組成物

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PCT/JP2013/067744 WO2013191302A1 (fr) 2012-06-21 2013-06-21 Composition cosmétique liquide comprenant une huile hydrocarbonée non volatile, une huile de diméthicone non volatile et un ester de dextrine

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FR3031674A1 (fr) * 2015-01-21 2016-07-22 Oreal Emulsion huile / huile renfermant des microparticules comprenant au moins deux materiaux differents, chacun organique ou inorganique
FR3031673A1 (fr) * 2015-01-21 2016-07-22 Oreal Emulsion h/h renfermant des microparticules a rupture de courbe, compositions les comprenant et utilisation des microparticules pour stabiliser les emulsions h/h
WO2017128099A1 (fr) * 2016-01-27 2017-08-03 L'oreal Composition anhydre non collante
US20190038536A1 (en) * 2015-09-25 2019-02-07 L'oreal Liquid cosmetic composition comprising a high non-volatile oil content and lip treatment process
FR3147716A1 (fr) * 2023-04-17 2024-10-18 L'oreal Composition cosmétique liquide comprenant des huiles de silicone, et des huiles à base d’hydrocarbures, et leurs procédés

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JP6320797B2 (ja) * 2013-03-12 2018-05-09 株式会社コーセー 液状口唇化粧料
CN111803404B (zh) * 2020-07-29 2021-06-15 深圳市兰亭科技股份有限公司 双体系组合物及其制备方法
FR3135895A1 (fr) * 2022-05-02 2023-12-01 Biosynthis Melange a base de polyester procede de preparation et composition cosmetique

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WO2015008263A1 (fr) * 2013-07-18 2015-01-22 L'oreal Émulsions huile/huile contenant des particules avec rupture de courbure, compositions les comprenant et utilisation des particules pour stabiliser des émulsions huile/huile
FR3008617A1 (fr) * 2013-07-18 2015-01-23 Oreal Emulsions pickering huile/huile renfermant des particules a rupture de courbe, compositions les comprenant et utilisation des particules pour stabiliser des emulsions h/h de pickering
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CN105392530B (zh) * 2013-07-18 2018-06-01 欧莱雅 包含具有曲率断裂的颗粒的油/油乳液、包含它们的组合物及该颗粒用于稳定o/o乳液的用途
FR3031674A1 (fr) * 2015-01-21 2016-07-22 Oreal Emulsion huile / huile renfermant des microparticules comprenant au moins deux materiaux differents, chacun organique ou inorganique
FR3031673A1 (fr) * 2015-01-21 2016-07-22 Oreal Emulsion h/h renfermant des microparticules a rupture de courbe, compositions les comprenant et utilisation des microparticules pour stabiliser les emulsions h/h
WO2016116473A1 (fr) * 2015-01-21 2016-07-28 L'oreal Émulsion huile/huile contenant des microparticules comprenant au moins deux matériaux différents, chacun étant organique ou minéral
WO2016116475A1 (fr) * 2015-01-21 2016-07-28 L'oreal Émulsion h/h contenant des microparticules présentant une cassure dans la partie incurvée, compositions les contenant, et utilisation de microparticules pour stabiliser les émulsions h/h
US20190038536A1 (en) * 2015-09-25 2019-02-07 L'oreal Liquid cosmetic composition comprising a high non-volatile oil content and lip treatment process
WO2017128099A1 (fr) * 2016-01-27 2017-08-03 L'oreal Composition anhydre non collante
CN109310619A (zh) * 2016-01-27 2019-02-05 莱雅公司 具有不粘感的无水组合物
FR3147716A1 (fr) * 2023-04-17 2024-10-18 L'oreal Composition cosmétique liquide comprenant des huiles de silicone, et des huiles à base d’hydrocarbures, et leurs procédés

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