Liquid makeup composition comprising film-forming silicones, oils, a silicone gum and pigments, and process using same

Abstract

The present invention relates to a liquid cosmetic for making up human keratin materials, in particular the skin and / or the lips, preferably the lips, comprising: - at least 20% by weight of at least one first linear or branched, preferably saturated, non-polar hydrocarbon oil having from 8 to 16 carbon atoms, - at least one second oil chosen from volatile or nonvolatile silicone oils, - at least one silicone elastomer carried in a hydrocarbon or silicone oil which may or may not be identical to the first oil(s) or to the second oil(s), - at least one silicone resin, - at least one silicone polyamide, - at least one silicone gum, - at least 8% by weight of pigments, - optionally water at a content of less than 5% by weight, - the (silicone resin + silicone polyamide) / pigment(s) weight ratio being between 1 and 2.7. It also relates to a makeup process in which this composition is applied to said keratin materials.

Description

LIQUID MAKEUP COMPOSITION COMPRISING FILM-FORMING SILICONES, OILS, A SILICONE GUM AND PIGMENTS, AND PROCESS USING SAMEThe present invention relates to a liquid cosmetic composition for making up in particular the skin and / or the lips, comprising at least 20% by weight of at least one particular non-polar hydrocarbon oil, a silicone gum, silicone compounds chosen from oils, elastomers, resins and silicone polyamides, and pigments in determined proportions.Compositions intended to be applied, in particular to the lips, and providing a matte finish after application, are well known in the cosmetic field and most of the time have the characteristic of comprising high contents of volatile oils and / or fillers. The high content of volatile oil(s) makes it possible to further increase the content of solid particles in the deposit, such as fillers and pigments, once the composition has been applied and dried. As regards the fillers used in compositions providing a matte finish, organic particles are often found, in particular polymeric particles such as nylon, polytetrafluoroethylene, polyethylene, silicone resins or elastomers, or else mineral particles such as kaolin or silica for example. These fillers make it possible, inter alia, to partially absorb the remaining oily compounds, whether they originate from the composition or from the support to which the latter is applied (sebum). With the high contents of volatile oils and of solid particles in compositions with a matte rendering, the content of nonvolatile oils is consequently greatly reduced in the deposit after application and drying of the composition. This is why matte compositions are generally considered by users to be not very or not at all comfortable, once put in place, also giving rise to a sensation of drying of the support, in particular of the lips. When it comes to compositions that provide a matte finish with a good staying power, it is also possible to be confronted with the appearance of an additional tack phenomenon, due in particular to the presence of film-forming polymer(s), which further reduces the sensation of comfort of such compositions once applied.There are of course compositions that provide an improvement to this problem of comfort, affording matte deposits with a good staying power. However, the desire is to further improve this aspect while at the same time retaining a considerable matteness result, with colouration that can be intense and covering, without sacrificing the staying power or making the compositions overly tacky.The present invention therefore relates to a liquid cosmetic composition for making up human keratin materials, in particular the skin and / or the lips, preferably the lips, comprising:- at least 20% by weight, relative to the total weight of the composition, of at least one first linear or branched, preferably saturated, non-polar hydrocarbon oil having from 8 to 16 carbon atoms,- at least one second oil chosen from volatile or nonvolatile silicone oils,- at least one silicone elastomer carried in a, preferably volatile, hydrocarbon or silicone oil which may or may not be identical to the first oil(s) or to the second oil(s),- at least one silicone resin,- at least one silicone polyamide,- at least one silicone gum,- at least 8% by weight, preferably at least 10% by weight, relative to the total weight of the composition, of pigments,- optionally water at a content of less than 5% by weight, preferably less than 3% by weight, relative to the total weight of the composition,- the (silicone resin + silicone polyamide) / pigment(s) weight ratio being between 1 and 2.7, preferably between 1 and 2.5.It also relates to a makeup process, in which such a composition is applied to the human keratin materials, in particular to the lips.The compositions according to the invention are easy to apply, in a non-tacky deposit that is precise, fine, and does not migrate, in particular into the fine lines and wrinkles around the lips. The deposits obtained after application of the compositions according to the invention are comfortable, matte, homogeneous, covering and enable the obtaining of intense colourations. Moreover, the deposits have a very good staying power and do not transfer.These advantages, and others, of the present invention will become more clearly apparent on reading the description and the examples which will follow.FIRST NON-POLAR HYDROCARBON OILSAs indicated above, the composition according to the invention comprises at least one first linear or branched, preferably saturated, non-polar hydrocarbon oil having from 8 to 16 carbon atoms.For the purposes of the invention, the term "non-polar hydrocarbon oil" denotes a hydrocarbon oil constituted solely of carbon and hydrogen atoms.In addition, for the purposes of the invention, the term "oil" denotes a compound that is immiscible in water and liquid at 20°C and atmospheric pressure (1.013 × 105Pa).The term "immiscible in water" is understood to mean that the mixing of the same amount of water and of oil, after stirring, does not result in a stable solution comprising only a single phase, at ambient temperature and atmospheric pressure. Observation is carried out by eye or by means of a phase-contrast microscope, if necessary, on 100 g of mixture obtained after sufficient stirring with a Rayneri blender to produce a vortex within the mixture (by way of indication, from 200 to 1000 rev / min), the resulting mixture being left to stand, in a closed flask, for 24 hours at ambient temperature before observation.The first non-polar volatile hydrocarbon oils are preferably chosen from the following non-polar hydrocarbon oils:- branched C8-C16alkanes such as C8-C16 isoalkanes (also called isoparaffins) such as for example isodecane, isododecane, isohexadecane, the compounds having the following INCI names: C8-9 Isoalkane, C11-13 Isoalkane for example sold under the references Isopar E, Isopar L by the company Brenntag,- linear C8-C13alkanes, for example such as the n-dodecane (C12) and n-tetradecane (C14) sold by Sasol respectively under the references Parafol 12-97 and Parafol 14-97, and also mixtures thereof, C9-12 Alkane (INCI name) which is more particularly a mixture of linear C9 to C12 alkanes, for example sold under the reference Vegelight Silk by the company Biosynthis, the undecane-tridecane mixture (Cetiol UT), the mixtures of n-undecane (C11) and of n-tridecane (C13) obtained in examples 1 and 2 of the application WO2008 / 155059 from the company Cognis, and- mixtures thereof.Preferably, the composition comprises isododecane at least as first oil(s). Advantageously, the first oil is isododecane.The composition according to the invention comprises at least 20% by weight, relative to the total weight of the composition, of at least one first oil as described above.Preferably, the content of first oil(s) is between 20% and 45% by weight, preferably 25% and 35% by weight, relative to the total weight of the composition.SECOND SILICONE OILSThe composition according to the invention further comprises at least one second oil chosen from volatile or nonvolatile silicone oils and different from the silicone gums.For the purposes of the present invention, the term "silicone oil" is understood to mean an oil comprising at least one silicon atom, and in particular at least one Si-O group, and more particularly an organopolysiloxane.More particularly, a silicone oil has a viscosity of less than or equal to 100 000 cSt (at 25°C, measured by the standard ASTM D-445).Nonvolatile silicone oilsThe term "nonvolatile oil" is understood to mean an oil that remains on the skin at ambient temperature and atmospheric pressure for at least several hours. In particular, these oils have a vapour pressure of less than 2.66 Pa, preferably less than 0.13 Pa. By way of example, the vapour pressure may be measured via the static method or via the effusion method by isothermal thermogravimetry, depending on the vapour pressure (OECD standard 104).Among the nonvolatile silicone oils, mention may be made of non-phenyl silicones and phenyl silicones optionally bearing a dimethicone fragment.The term "non-phenyl silicone oil" denotes a silicone oil not comprising any phenyl substituents.It should be noted that the term "dimethicone fragment" denotes a divalent siloxane group in which the silicon atom bears two methyl radicals, this group not being located at the ends of the molecule. It may be represented by the following formula:-(Si(CH3)2-O)-.More particularly, said silicone oils are free of (poly)alkoxylated groups, in particular such as (poly)ethoxylated or (poly)propoxylated groups, or (poly)glycerolated groups.In particular, the non-phenyl silicones may be chosen from the following nonvolatile oils:- polydimethylsiloxanes (INCI name: Dimethicone), for example the products of the Belsil DM range from Wacker; Xiameter PMX-200 range from Dow Corning,- alkyl dimethicones comprising aliphatic groups, in particular alkyl or alkoxy groups, which are pendent and / or at the end of the silicone chain, these groups each comprising from 2 to 24 carbon atoms. By way of example, mention may be made of the Cetyl Dimethicone (INCI name) sold under the commercial reference Abil Wax 9801 from Evonik Goldschmidt,- mixtures thereof.Preferably, these nonvolatile non-phenyl silicone oils are chosen from polydimethylsiloxanes.As regards the phenyl silicones, mention may be made of the oils having the following INCI names: Trimethyl Pentaphenyl Trisiloxane, Tetramethyl Tetraphenyl Trisiloxane, Diphenyl Dimethicone, Trimethylsiloxyphenyl Dimethicone, Phenyl Trimethicone, Diphenylsiloxy Phenyl Trimethicone, and also mixtures thereof.These products are sold in particular under the names PH-1555 HRI Cosmetic Fluid (Trimethyl Pentaphenyl Trisiloxane) and Dow Corning 556 Cosmetic Grade Fluid (Phenyl Trimethicone) by Dow Corning; Diphenyl Dimethicones such as the products KF-54, KF54HV, KF-50-300CS, KF-53 d and KF-50-100CS or Diphenylsiloxy Phenyl Trimethicone KF56 A sold by Shin-Etsu; the products Belsil PDM 1000 and Belsil PDM 20 sold by Wacker Chemie (Trimethylsiloxy Phenyl Dimethicone), alone or as mixtures. The values in parentheses represent the viscosities at 25°C (ASTM D-445 standard).Preferably, the composition comprises at least one nonvolatile silicone oil chosen from polydimethylsiloxanes, from phenyl silicone oils, preferably not comprising a dimethicone fragment, and also mixtures thereof.In accordance with a more advantageous embodiment, the second oil is chosen from nonvolatile, non-phenyl silicone oils, preferably polydimethylsiloxanes.Volatile silicone oilsThe composition according to the invention may optionally comprise at least one volatile silicone oil.The term "volatile oil" is understood to mean an oil having a non-zero vapour pressure at ambient temperature and atmospheric pressure, ranging in particular from 2.66 Pa to 40 000 Pa, in particular ranging to 13 000 Pa, and more particularly ranging to 1300 Pa (OECD standard 104).The volatile silicone oils may be chosen from linear, branched or cyclic silicone oils, such as polydimethylsiloxanes having from 3 to 7 silicon atoms.As examples of such oils, mention may be made of the oils having the following INCI names: Cyclopentasiloxane, Cyclotetrasiloxane, Cyclohexasiloxane, Caprylyl Methicone, Disiloxane, Trisiloxane, Dimethicones in particular with a viscosity of less than 5 cSt, such as those sold under the reference Xiameter PMX-200 Silicone Fluid, sold by the company Dow Corning, with viscosities in particular of 1 cSt, 1.5 cSt, 3 cSt, or also KF 96 L 2 cs from Shin Etsu, alone or as mixtures.In accordance with one advantageous embodiment, the second volatile silicone oil is chosen from linear silicone oils.According to one embodiment, the composition comprises, as second silicone oil(s), at least one volatile, preferably linear, silicone oil, and at least one nonvolatile, preferably non-phenyl, silicone oil.In accordance with a particular embodiment of the invention, the content of second silicone oil(s) ranges from 25% to 35% by weight, preferably from 27% to 32% by weight, relative to the weight of the composition.More particularly, the content of second nonvolatile silicone oil(s) ranges from 8% to 15% by weight, preferably 10% to 13% by weight, relative to the total weight of the composition.SILICONE RESINThe composition according to the invention comprises at least one silicone resin.More generally, the term "resin" means a compound of which the structure is three-dimensional. Thus, for the purposes of the present invention, a polydimethylsiloxane is not a silicone resin.The nomenclature of silicone resins (also known as siloxane resins) is known under the name “MDTQ”, the resin being described as a function of the various siloxane monomer units it comprises, each of the letters MDTQ characterizing a type of unit:The letter "M" represents the monofunctional unit of formula R1R2R3SiO1 / 2, the silicon atom being bonded to just one oxygen atom in the polymer comprising this unit.The letter "D" means a difunctional unit R1R2SiO2 / 2in which the silicon atom is bonded to two oxygen atoms.The letter "T" represents a trifunctional unit of formula R1SiO3 / 2.In the units M, D and T defined previously, Ri, namely R1, R2 and R3, which may be identical or different, represent a hydrocarbon radical (especially alkyl) having from 1 to 10 carbon atoms, a phenyl group, a phenylalkyl group or a hydroxyl group.Lastly, the letter "Q" means a tetrafunctional unit SiO4 / 2in which the silicon atom is bonded to four oxygen atoms, which are themselves bonded to the rest of the polymer.Such resins are described, for example, in the Encyclopedia of Polymer Science and Engineering, vol. 15, John Wiley and Sons, New York, (1989), pp. 265-270, and US 2 676 182, US 3 627 851, US 3 772 247, US 5 248 739 or else US 5 082 706, US 5 319 040, US 5 302 685 and US 4 935 484.Various silicone resins with different properties may be obtained from these different units, the properties of these polymers varying as a function of the type of monomer (or unit), the nature and number of the radical(s) Ri, the length of the polymer chain, the degree of branching and the size of the side chains.As silicone resins that may be used in the compositions according to the invention, use may be made, for example, of silicone resins of MQ type, of T type or of MQT type.MQ resinsAs examples of silicone resins of MQ type, mention may be made of resins of siloxysilicate type, such as the alkylsiloxysilicates, arylsiloxysilicates or alkylarylsiloxysilicates, of formula [(R1)3SiO1 / 2]x(SiO4 / 2)y(MQ units) in which x and y are integers ranging for example from 50 to 80, and such that the group R1 represents a radical as defined previously, and is preferably an alkyl group having from 1 to 8 carbon atoms or a hydroxyl group, preferably a methyl group.The silicone resin can be used alone or else in the form of a mixture in an oil, which can in particular be chosen from the first and second oil(s) and also combinations thereof.As examples of MQ-type silicone resins of Trimethylsiloxysilicate (INCI name) type, mention may be made of those sold under the reference SR1000 by the company General Electric, under the reference TMS 803 by the company Wacker, or else mixtures comprising same such as the products sold under the names KF-7312J (in cyclopentasiloxane) by the company Shin-Etsu, Silsoft 74 Fluid (in isododecane) by the company Momentive, Dowsil RSN-749 Resin (in cyclopentasiloxane), Dowsil 593 Fluid (in a dimethicone) by the company Dow Corning.As silicone resins comprising MQ siloxysilicate units, mention may also be made of the phenylalkylsiloxysilicate resins, such as phenylpropyldimethylsiloxysilicate (INCI name; Silshine 151 sold by the company General Electric). The preparation of such resins is described in particular in patent US 5 817 302.T resinsAs examples of silicone resins of type T, mention may be made of the polysilsesquioxanes comprising predominantly units of formula (RSiO3 / 2)x(T units) in which x is greater than 100 and such that the group R is an alkyl group having from 1 to 10 carbon atoms, said polysilsesquioxanes possibly also comprising Si-OH end groups. Thus, these resins comprise for example at least 80 mol% of T units.Mention may be made of polymethylsilsesquioxanes, which are polysilsesquioxanes in which none of the methyl radicals is substituted by another group. Such polymethylsilsesquioxanes are described, for example, in the document US 5 246 694.Preferably, use may be made of the Polymethylsilsesquioxane (INCI name) resins in which R represents a methyl group, such as for example those sold by the company Wacker under the reference Resin MK, such as Belsil PMS MK, and by the company Shin-Etsu under the references KR-220L or also under the reference KR-251.Among the silsesquioxane resins that may be used in the present invention, mention may also be made of those corresponding to silsesquioxane homopolymers and / or copolymers having an average siloxane unit of general formula R1n SiO(4-n) / 2, in which each R1 is a propyl group, in which more than 80 mol% of R1 represent a C3 to C10 alkyl group, n is a value from 1.0 to 1.4, and more than 60 mol% of the copolymer comprises R1SiO3 / 2 units. Since each R1 is a propyl group, these polymers are called polypropylsilsesquioxane resins (INCI name) or "t-propyl" silsesquioxane resins. These resins and the processes for producing them are described for example in documents US8586013, US2012 / 0301415 and US2006 / 0292096.Among the polypropylsilsesquioxane resins suitable for use in the present invention, mention may be made of those sold by Dow Corning under the names Dowsil 670 Fluid or Dowsil 680 ID Fluid, which are mixtures of Polypropylsilsesquioxane respectively with cyclopentasiloxane or with isododecane.MQT resinsResins comprising MQT units that are known in particular are those cited in the document US 5 110 890.A preferred form of resins of MQT type are MQT-propyl (also known as MQTPr) resins. Such resins that may be used in the compositions according to the invention are especially the resins described and prepared in patent application WO 2005 / 075542, the content of which is incorporated herein by reference.The MQ-T-propyl resin preferably comprises the units:(i) (R13SiO1 / 2)a(ii) (R22SiO2 / 2)b(iii) (R3SiO3 / 2)cand(iv) (SiO4 / 2)dwithR1, R2 and R3 independently representing a hydrocarbon radical (in particular alkyl) having from 1 to 10 carbon atoms, a phenyl group, a phenylalkyl group or a hydroxyl group and preferably an alkyl radical having from 1 to 8 carbon atoms or a phenyl group,a, b, c and d being molar fractions,a being between 0.05 and 0.5,b being between zero and 0.3,c being greater than zero,d being between 0.05 and 0.6,a + b + c + d = 1,provided that more than 40 mol% of the R3 groups of the siloxane resin are propyl groups.Preferably, the siloxane resin comprises the units:(i) (R13SiO1 / 2)a(iii) (R3SiO3 / 2)cand(iv) (SiO4 / 2)dwithR1 and R3 independently representing an alkyl group having from 1 to 8 carbon atoms, R1 preferably being a methyl group and R3 preferably being a propyl group,a being between 0.05 and 0.5 and preferably between 0.15 and 0.4,c being greater than zero, preferably between 0.15 and 0.4,d being between 0.05 and 0.6, preferably between 0.2 and 0.6, or between 0.2 and 0.55,a + b + c + d = 1, and a, b, c and d being molar fractions,provided that more than 40 mol% of the R3 groups of the siloxane resin are propyl groups.The siloxane resins that may be used according to the invention may be obtained via a process comprising the reaction of:A) an MQ resin comprising at least 80 mol% of (R13SiO1 / 2)aand (SiO4 / 2)dunits,- R1 representing an alkyl group having from 1 to 8 carbon atoms, an aryl group, a carbinol group or an amino group,- a and d being greater than zero,- the ratio a / d being between 0.5 and 1.5; andB) a T-propyl resin comprising at least 80 mol% of (R3SiO3 / 2)cunits,- R3 representing an alkyl group having from 1 to 8 carbon atoms, an aryl group, a carbinol group or an amino group,- c being greater than zero,provided that at least 40 mol% of the R3 groups are propyl groups,wherein the mass ratio A / B is between 95:5 and 15:85 and preferably the mass ratio A / B is 30:70.Advantageously, the mass ratio A / B is between 95:5 and 15:85; preferably the ratio A / B is less than or equal to 70:30.Preferably, the composition according to the invention comprises, as silicone resin, at least one alkylsiloxysilicate, arylsiloxysilicate, alkylarylsiloxysilicate and polysilsesquioxane resin, and also mixtures thereof; more particularly from the silicone resins having the following INCI names: trimethylsiloxysilicate, polymethylsilsesquioxane, polypropylsilsesquioxane, and also mixtures thereof. Preferably, the composition according to the invention comprises at least one trimethylsiloxysilicate resin.Advantageously, the silicone resin is present in a content ranging from 10% to 20% by weight, preferably in a content ranging from 12% to 18% by weight, relative to the total weight of the composition.As indicated above, the (silicone resin + silicone polyamide) / pigment(s) weight ratio is between 1 and 2.7, preferably between 1 and 2.5. It is specified that for this calculation the contents of silicone resin and of silicone polyamide are considered in terms of active material.Moreover, if the composition comprises mica as filler, the content thereof is taken into account in the calculation of said weight ratio, with the content of pigment(s). It should be noted that in this calculation the silicone resin does not take into account the possible presence of a silicone wax, more particularly the presence of C30-45 polypropylsilsesquioxane in the composition.SILICONE ELASTOMERThe composition according to the invention also comprises at least one silicone elastomer carried in at least one oil identical to or different from the first or second oil.For the purposes of the invention, the term "carried" is understood to mean that the silicone elastomer is introduced into the composition in a form predispersed in at least one oil. More particularly, the elastomer is in the form of a homogeneous mixture in said oil or mixture of oils, which is stable for at least 24 hours at 20°C. Preferably, this elastomer is in the form of a gel in at least one oil. In particular, a powder of silicone elastomer suspended in at least one such oil is not considered, for the purposes of the invention, to be an organopolysiloxane elastomer carried in at least one oil.The term "elastomer of silicone", "silicone elastomer" or "polyorganosiloxane elastomer" is understood to mean a flexible, deformable, crosslinked organopolysiloxane having viscoelastic properties and in particular the consistency of a sponge or a flexible sphere. Its modulus of elasticity is such that this material withstands deformation and possesses a limited stretchability and contractability. This material is capable of regaining its original shape after stretching.In these gels, the organopolysiloxane particles may be spherical or non-spherical particles.The silicone elastomer present in the composition according to the invention is preferably a non-emulsifying silicone elastomer.The term "non-emulsifying" defines silicone elastomers containing no hydrophilic chain, and in particular containing no polyoxyalkylene (especially polyoxyethylene or polyoxypropylene) units or polyglyceryl units.Thus, the silicone 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, or else hydrocarbon chain having an ethylenic unsaturation at each end, in particular in the presence of a platinum catalyst; or by dehydrogenation crosslinking condensation reaction between a hydroxyl-terminated diorganopolysiloxane and a diorganopolysiloxane containing at least one hydrogen bonded to silicon, in particular in the presence of an organotin; or by crosslinking condensation reaction of a hydroxyl-terminated diorganopolysiloxane and of a hydrolysable organopolysilane; or by thermal crosslinking of organopolysiloxane, in particular in the presence of an organoperoxide catalyst; or by crosslinking of organopolysiloxane via high-energy radiation such as gamma rays, ultraviolet rays or an electron beam.According to a first preferred embodiment, the organopolysiloxane elastomer is obtained by crosslinking addition reaction (A) of diorganopolysiloxane containing at least two hydrogens each bonded to a silicon, and (B) of diorganopolysiloxane containing at least two ethylenically unsaturated groups bonded to silicon, in particular in the presence (C) of a platinum catalyst, as described, for example, in patent application EP 295 886.In particular, the organopolysiloxane elastomer may be obtained by reaction of dimethylvinylsiloxy-terminated dimethylpolysiloxane and of trimethylsiloxy-terminated methylhydropolysiloxane, in the presence of a platinum catalyst.Compound (A) is the base reactant for the formation of elastomeric organopolysiloxane, and the crosslinking is performed by addition reaction of compound (A) with compound (B) in the presence of catalyst (C).Compound (A) is in particular an organopolysiloxane containing at least two hydrogen atoms bonded to different silicon atoms in each molecule.Compound (A) can have any molecular structure, in particular a linear-chain or branched-chain structure or a cyclic structure.Compound (A) can have a viscosity at 25°C ranging from 1 to 50 000 centistokes, in particular in order to be readily miscible with compound (B).The organic groups bonded to the silicon atoms of compound (A) may be alkyl groups such as methyl, ethyl, propyl, butyl, octyl; substituted alkyl groups such as 2-phenylethyl, 2-phenylpropyl or 3,3,3-trifluoropropyl; aryl groups such as phenyl, tolyl, xylyl; substituted aryl groups such as phenylethyl; and substituted monovalent hydrocarbon groups such as an epoxy group, a carboxylate ester group or a mercapto group.Compound (A) can thus be chosen from trimethylsiloxy-terminated methylhydropolysiloxanes, trimethylsiloxy-terminated dimethylsiloxane / methylhydrosiloxane copolymers or cyclic dimethylsiloxane / methylhydrosiloxane copolymers.Compound (B) is advantageously a diorganopolysiloxane having at least two lower (for example C2-C4) alkenyl groups; the lower alkenyl group can be chosen from vinyl, allyl and propenyl groups. These lower alkenyl groups can be located at any position of the organopolysiloxane molecule but are preferably located at the ends of the organopolysiloxane molecule. The organopolysiloxane (B) may have a branched-chain, linear-chain, cyclic or network structure but the linear-chain structure is preferred. Compound (B) can have a viscosity ranging from the liquid state to the gum state. Preferably, compound (B) has a viscosity of at least 100 centistokes at 25°C.Besides the abovementioned alkenyl groups, the other organic groups bonded to the silicon atoms in compound (B) may be alkyl groups such as methyl, ethyl, propyl, butyl or octyl; substituted alkyl groups such as 2-phenylethyl, 2-phenylpropyl or 3,3,3-trifluoropropyl; aryl groups such as phenyl, tolyl or xylyl; substituted aryl groups such as phenylethyl; and substituted monovalent hydrocarbon groups such as an epoxy group, a carboxylate ester group or a mercapto group.The organopolysiloxanes (B) may be chosen from methylvinylpolysiloxanes, methylvinylsiloxane / dimethylsiloxane copolymers, dimethylvinylsiloxy-terminated dimethylpolysiloxanes, dimethylvinylsiloxy-terminated dimethylsiloxane / methylphenylsiloxane copolymers, dimethylvinylsiloxy-terminated dimethylsiloxane / diphenylsiloxane / methylvinylsiloxane copolymers, trimethylsiloxy-terminated dimethylsiloxane / methylvinylsiloxane copolymers, trimethylsiloxy-terminated dimethylsiloxane / methylphenylsiloxane / methylvinylsiloxane copolymers, dimethylvinylsiloxy-terminated methyl(3,3,3-trifluoropropyl)polysiloxanes, and dimethylvinylsiloxy-terminated dimethylsiloxane / methyl(3,3,3-trifluoropropyl)siloxane copolymers.In particular, the elastomeric organopolysiloxane may be obtained via reaction of dimethylvinylsiloxy-terminated dimethylpolysiloxane and of trimethylsiloxy-terminated methylhydropolysiloxane, in the presence of a platinum catalyst.Advantageously, the sum of the number of ethylenic groups per molecule of compound (B) and of the number of hydrogen atoms bonded to silicon atoms per molecule of compound (A) is at least 5.It is advantageous for compound (A) to be added in an amount such that the molecular ratio of the total amount of hydrogen atoms bonded to silicon atoms in compound (A) to the total amount of all the ethylenically unsaturated groups in compound (B) is within the range from 1.5 / 1 to 20 / 1.Compound (C) is the catalyst for the crosslinking reaction, and is in particular chloroplatinic acid, chloroplatinic acid-olefin complexes, chloroplatinic acid-alkenylsiloxane complexes, chloroplatinic acid-diketone complexes, platinum black and platinum on a support.Catalyst (C) is preferably added in an amount of from 0.1 to 1000 parts by weight and better still from 1 to 100 parts by weight, as clean platinum metal, per 1000 parts by weight of the total amount of compounds (A) and (B).According to a second preferred embodiment of the invention, the organopolysiloxane elastomer is obtained by reaction (A) of a polysiloxane comprising at least two hydrogens each bonded to a silicon, and (B) of an α,ω-diene of formula CH2=CH(CH2)xCH=CH2in which x ranges from 1 to 20, in particular from 4 to 19, especially in the presence of a platinum-based catalyst, and (C) of a low-molecular-weight silicone, preferably a volatile silicone, as described for example in patent US5654362.Non-emulsifying elastomers are described in particular in patents EP242219, EP295886, EP765656 and US5654362 and in patent application JPS61194009.In particular, the silicone elastomer used in the present invention is chosen from the compounds having the following INCI names: Dimethicone Crosspolymer, Dimethicone / Vinyl Dimethicone Crosspolymer, Vinyl Dimethicone / Lauryl Dimethicone Crosspolymer, Dimethicone / Vinyltrimethylsiloxysilicate Crosspolymer, Dimethicone Crosspolymer-3, and preferably from Dimethicone Crosspolymer.As mentioned above, the elastomer present in the composition according to the invention is in a form carried in an oil which may be identical to or different from the first and second oils, and also the additional oils, described below and to the descriptions of which reference may be made.Thus, the oil is chosen from silicone oils and from polar or non-polar, volatile or nonvolatile, hydrocarbon oils.According to a first embodiment of the invention, the oil carrying the silicone elastomer is chosen from linear or cyclic, preferably linear, volatile silicone oils.According to a second embodiment, the oil carrying the silicone elastomer is chosen from nonvolatile phenyl or non-phenyl silicone oils, in particular having the following INCI names: Dimethicone, Methyl Trimethicone, Phenyl Methicone, Phenyl Dimethicone and Phenyl Trimethicone.Preferably, the oil carrying the silicone elastomer is chosen from silicone oils chosen from the Dimethicones, especially having a viscosity ranging from 1 to 500 cSt at 25°C.According to a final particular embodiment of the invention, the oil carrying the silicone elastomer is chosen from volatile hydrocarbon oils, for example isododecane, or polar nonvolatile hydrocarbon oils, such as for example esters, such as triethylhexanoin and plant oils, or also non-polar nonvolatile hydrocarbon oils, such as for example squalane. Preferably, the oil carrying the silicone elastomer is chosen from volatile hydrocarbon oils, for example isododecane.Preferably, the oil carrying the silicone elastomer is chosen from the Dimethicones, in particular having a viscosity ranging from 1 to 500 cSt at 25°C, and from isododecane, alone or as a mixture.As non-emulsifying elastomers, use may be made more particularly of those sold under the names KSG-6, KSG-15, KSG-16, KSG-016F, KSG-18A, KSG-41, KSG-42, KSG-43, KSG-44, USG-102, USG-103, USG-105, USG-106 and USG-107A, by the company Shin Etsu; Dowsil DC9040 Silicone Elastomer Blend, Dowsil DC9041 Silicone Elastomer Blend, Dowsil 9045 Silicone Elastomer Blend, Dowsil 9350 Elastomer Blend, Dowsil 9546 Silicone Elastomer Blend, Dowsil EL-9240 Silicone Elastomer Blend, Dowsil EL-9241 Silicone Elastomer Blend, Dowsil EL-9140 DM Silicone Elastomer Blend, Dowsil EL-8040 ID, by the company Dow Chemical Company; SFE 839 Gel by the company Momentive Performance Materials.According to another variant, the elastomer may be an emulsifying elastomer.As emulsifying silicone elastomer, mention may be made of silicone polyether elastomers, polyglyceryl silicone elastomers, polyether dimethicone copolymers and mixtures thereof.The emulsifying silicone elastomers may include functional groups chosen from the group comprising polyglycerol, polyethylene glycol or polypropylene glycol. For example, mention may be made of Dimethicone (and) Dimethicone / PEG-10 / 15 Crosspolymer, sold under the name KSG-210®, and Dimethicone (and) Dimethicone / Polyglycerin-3 Crosspolymer, sold under the name KSG-710®, Squalane (and) Lauryl Dimethicone / Polyglycerin-3 Crosspolymer, sold under the name KSG-840®, by the company Shin Etsu. Mention may also be made of PEG-10 Dimethicone sold under the name KF-6017®by Shin Etsu, Dimethicone (and) PEG / PPG-18 / 18 Dimethicone sold under the name ES-5226 DM®by the company Dow Corning Corporation, PEG-9 Polydimethylsiloxyethyl Dimethicone (and) PEG-9 sold under the name KF-6028®, and Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone sold under the name KF-6038®, by the company Shin Etsu.Preferably, the composition according to the invention comprises at least one non-emulsifying silicone elastomer.The content of silicone elastomer, expressed as active material, ranges from 2 to 8% by weight, preferably from 2.5 to 6% by weight, relative to the total weight of the composition.SILICONE POLYAMIDEThe composition according to the invention also comprises at least one silicone polyamide.The silicone polyamides of the composition are preferably solid at 20°C and atmospheric pressure (1.013 × 105Pa).For the purposes of the invention, the term "polymer" is understood to mean a compound containing at least 2 repeating units, preferably at least 3 repeating units and better still 10 repeating units.The silicone polyamides of the composition of the invention may be polymers of the polyorganosiloxane type, for example such as those described in the documents US5874069, US5919441, US6051216 and US5981680. According to the invention, the silicone polymers may belong to the following two families:(1) polyorganosiloxanes comprising at least two amide groups, these two groups being located in the chain of the polymer, and / or(2) polyorganosiloxanes comprising at least two amide groups, these two groups being located on grafts or branches.A) According to a first variant, the silicone polymers are polyorganosiloxanes as defined above in which the amide units are arranged in the chain of the polymer.The silicone polyamides may more particularly be polymers comprising at least one unit corresponding to the general formula (I):1) in which: G’ represents C(O) when G represents -C(O)-NH-Y-NH-, and G’ represents –NH- when G represents –NH-C(O)-Y-C(O)-,2) R4, R5, R6and R7, which may be identical or different, represent a group chosen from:- saturated or unsaturated, linear, branched or cyclic C1to C40hydrocarbon groups, which may contain in their chain one or more oxygen, sulfur and / or nitrogen atoms, and which may be partially or completely substituted by fluorine atoms,- C6to C10aryl groups, optionally substituted by one or more C1to C4alkyl groups,- polyorganosiloxane chains possibly containing one or more oxygen, sulfur and / or nitrogen atoms,3) the groups X, which may be identical or different, represent a linear or branched C1to C30alkylenediyl group, possibly containing in its chain one or more oxygen and / or nitrogen atoms,4) Y is a saturated or unsaturated, divalent C1to C50, linear or branched alkylene, arylene, cycloalkylene, alkylarylene or arylalkylene group, which may comprise one or more oxygen, sulfur and / or nitrogen atoms, and / or may bear as substituent one of the following atoms or groups of atoms: fluorine, hydroxyl, C3to C8cycloalkyl, C1to C40alkyl, C5to C10aryl, phenyl optionally substituted by 1 to 3 C1to C3alkyl, C1to C3hydroxyalkyl and C1to C6aminoalkyl groups, or5) Y represents a group corresponding to the formula: R8-T<; in which- T represents a linear or branched, saturated or unsaturated, trivalent or tetravalent C3to C24hydrocarbon group optionally substituted by a polyorganosiloxane chain, and possibly containing one or more atoms chosen from O, N and S, or T represents a trivalent atom chosen from N, P and Al, and- R8represents a linear or branched C1to C50alkyl group or a polyorganosiloxane chain, possibly comprising one or more ester, amide, urethane, thiocarbamate, urea, thiourea and / or sulfonamide groups, which may possibly be linked to another chain of the polymer,6) n is an integer ranging from 2 to 500, preferably from 2 to 200, and m is an integer ranging from 50 to 1000, preferably from 50 to 700 and better still from 50 to 200.It will be noted that "m" corresponds to the average degree of polymerization of the silicone portion of the silicone polyamide.According to one embodiment of the invention, 80% of the groups R4, R5, R6and R7of the polymer are preferably chosen from methyl, ethyl, phenyl and 3,3,3-trifluoropropyl groups. According to another embodiment, 80% of the groups R4, R5, R6and R7of the polymer are methyl groups.According to the invention, Y may represent various divalent groups, furthermore optionally comprising one or two free valencies for establishing bonds with other units of the polymer or copolymer. Preferably, Y represents a group chosen from:a) linear C1to C20, preferably C1to C10, alkylene groups,b) branched C30to C56alkylene groups possibly comprising rings and unconjugated unsaturations,c) C5-C6cycloalkylene groups,d) phenylene groups optionally substituted with one or more C1to C40alkyl groups,e) C1to C20alkylene groups comprising from 1 to 5 amide groups,f) C1to C20alkylene groups, comprising one or more substituents chosen from hydroxyl, C3to C8cycloalkane, C1to C3hydroxyalkyl and C1to C6alkylamine groups,g) polyorganosiloxane chains of formula:in which R4, R5, R6, R7, T and m are as defined above.B) According to the second variant, the silicone polyamides may be polymers comprising at least one unit corresponding to the formula (II):in which:- R4and R6, which may be identical or different, are as defined above for the formula (I),- R10represents a group as defined above for R4and R6, or represents the group of formula -X-G’’-R12in which X is as defined above for the formula (I) and R12represents a hydrogen atom or a saturated or unsaturated, linear, branched or cyclic, C1to C50hydrocarbon group optionally comprising in its chain one or more atoms chosen from O, S and N, optionally substituted by one or more fluorine atoms and / or one or more hydroxyl groups, or a phenyl group optionally substituted by one or more C1to C4alkyl groups, and G’’ represents ––C(O)NH- and –HN-C(O)-.- R11represents the group of formula -X-G’’-R12in which X, G’’ and R12are as defined above,- m1is an integer ranging from 50 to 998, and- m2is an integer ranging from 2 to 500.It will be noted that "m1" corresponds to the average degree of polymerization of the silicone portion of the silicone polyamide.According to the invention, the silicone polymer may be a homopolymer, i.e. a polymer comprising a plurality of identical units, in particular units of formula (I) or of formula (II).According to the invention, it is also possible to use a polymer constituted of a copolymer comprising a plurality of different units of formula (I), i.e. a polymer in which at least one of R4, R5, R6, R7, X, G, Y, m and n is different in one of the units. The copolymer may also be formed from a plurality of units of formula (II), in which at least one of R4, R6, R10, R11, m1and m2is different in at least one of the units.It is also possible to use a polymer comprising at least one unit of formula (I) and at least one unit of formula (II), the units of formula (I) and the units of formula (II) possibly being identical to or different from one another.According to one variant of the invention, it is also possible to use a silicone polyamide furthermore comprising at least one hydrocarbon unit comprising two groups capable of establishing hydrogen interactions, chosen from ester, amide, sulfonamide, carbamate, thiocarbamate, urea, urethane, thiourea, oxamido, guanidino and biguanidino groups, and combinations thereof.These copolymers may be block polymers, sequenced polymers or grafted polymers.In formulae (I) and (II), the alkylene group representing X or Y can optionally contain in its alkylene part at least one of the following components:1) 1 to 5 amide, urea, urethane or carbamate groups,2) a C5or C6cycloalkyl group, and3) a phenylene group optionally substituted by 1 to 3 identical or different C1to C3alkyl groups.In formulae (I) and (II), the alkylene groups may also be substituted by at least one component chosen from the group consisting of:- a hydroxy group,- a C3to C8cycloalkyl group,- one to three C1to C40alkyl groups,- a phenyl group optionally substituted by one to three C1to C3alkyl groups,- a C1to C3hydroxyalkyl group, and- a C1to C6aminoalkyl group.In these formulae (I) and (II), Y may also represent the formula R8–T<; where R8represents a polyorganosiloxane chain and T represents a group of formula:in which a, b and c are independently integers ranging from 1 to 10, and R13is a hydrogen atom or a group such as those defined for R4, R5, R6and R7.In formulae (I) and (II), R4, R5, R6and R7preferably represent, independently, a linear or branched C1to C40alkyl group, preferably a CH3, C2H5, n-C3H7or isopropyl group, a polyorganosiloxane chain or a phenyl group optionally substituted by one to three methyl or ethyl groups.As has been seen previously, the polymer may comprise identical or different units of formula (I) or (II).Thus, the polymer may be a polyamide containing a plurality of units of formula (I) or (II) of different lengths, i.e. a polyamide corresponding to the formula (III):in which X, Y, n and R4to R7have the meanings given above, m1and m2, which are different, are chosen in the range extending from 1 to 1000, and p is an integer ranging from 2 to 300.In this formula, the units may be structured to form either a block copolymer or a random copolymer or an alternating copolymer. In this copolymer, the units may be not only of different lengths, but also of different chemical structures, for example containing different Y groups. In this case, the polymer may correspond to the formula (IV):in which R4to R7, X, Y, m1, m2, n and p have the meanings given above and Y1is different from Y but chosen from the groups defined for Y. As previously, the various units may be structured to form either a block copolymer or a random copolymer or an alternating copolymer.In this first embodiment of the invention, the silicone polymer may also be constituted of a grafted copolymer. Thus, the polyamide containing silicone units may be grafted and optionally crosslinked by silicone chains containing amide groups. Such polymers may be synthesized with trifunctional amines.According to the invention, as has been seen previously, the siloxane units may be in the main chain or backbone of the polymer, but they may also be present in grafted or pendent chains. In the main chain, the siloxane units may be in the form of segments as described above. In the pendent or grafted chains, the siloxane units may appear individually or in segments.According to one embodiment variant of the invention, a copolymer of silicone polyamide and of hydrocarbon-based polyamide, or a copolymer comprising units of formula (I) or (II) and hydrocarbon-based polyamide units, may be used. In this case, the polyamide-silicone units may be arranged at the ends of the hydrocarbon-based polyamide.Advantageously, the composition comprises at least one polyamide / polydimethylsiloxane polymer, especially a polymer of general formula (I) with an index m with a value of greater than 50, in particular greater than 75 and especially of about 100.Advantageously, the silicone polyamide of formula (I) has a weight-average molecular mass ranging from 10 000 to 500 000 g / mol.More preferably, X and Y independently represent a group chosen from linear C1to C20, preferably C1to C10, alkylene groups.As examples of silicone polyamide, mention may be made of one of the silicone polyamides obtained in accordance with examples 1 to 3 of the document US5981680, and also the product sold under the reference DC 2-8179 by Dow Corning (INCI name: Nylon-611 / Dimethicone Copolymer).According to one embodiment variant of the invention, the polymer is constituted of a homopolymer or copolymer comprising urethane or urea groups. These polymers are described in detail in patent application WO 2003 / 106614.The composition may contain, instead of the silicone polyamide, a polyorganosiloxane polymer containing two or more urethane and / or urea groups, either in the backbone of the polymer or on side chains or as pendent groups.Polymers comprising at least two urethane and / or urea groups in the backbone may be polymers comprising at least one unit corresponding to the following formula:in which R4, R5, R6, R7, X, Y, m and n have the meanings given above for the formula (I), and U represents -O- or –NH-, such that: - U – C(=O) – NH -; corresponds to a urethane or urea group.In this formula, Y may be a linear or branched C1to C40alkylene group, optionally substituted by a C1to C15alkyl group or a C5to C10aryl group. Preferably, a -(CH2)6- group is used.The polymer constituting the silicone polymer may be formed from silicone-urethane and / or silicone-urea units of different length and / or constitution, and may be in the form of block, sequenced or statistical (random) copolymers.As in the case of the silicone polyamides of formula (I), (II) or (III), silicone polyurethanes or polyureas having units of different length and structure, in particular units of lengths differing via the number of silicone units, may be used in the invention.The polymers and copolymers used in the composition of the invention advantageously have a solid state to liquid state transition temperature ranging from 45°C to 190°C. Preferably, they have a solid state to liquid state transition temperature ranging from 70 to 130°C and better still from 80°C to 105°C.Advantageously, the silicone polyamide has a weight-average molecular mass of between 10 000 and 500 000 g / mol.Preferably, the silicone polyamide is present in the composition in a content ranging from 5% to 12% by weight, preferably from 6% to 10% by weight, relative to the total weight of the composition.SILICONE GUMThe composition according to the invention also comprises at least one silicone gum.More particularly, the silicone gum is chosen from the polyorganosiloxanes with a weight-average molecular mass of greater than or equal to 400 000 g / mol.The weight-average molecular masses are measured in a manner conventional in the field, for example using size-exclusion chromatography (SEC).Preferably, the viscosity of the silicone gum is greater than or equal to 300 000 cSt, advantageously greater than or equal to 400 000 cSt, more particularly greater than or equal to 800 000 cSt, and more particularly less than or equal to 10 000 000 cSt (at 25°C, measured by the standard ASTM D-445), more particularly between 1 000 000 and 5 000 000 cSt (at 25°C, measured by the standard ASTM D-445).According to the present invention, a silicone gum is not considered to be a silicone oil.The term "silicone gum" is more particularly understood to mean polyorganosiloxanes, in particular linear non-crosslinked, optionally hydroxylated, phenylated or vinyl polydimethylsiloxanes, or combinations thereof. Consequently, the silicone gums used according to the invention are not silicone elastomers.According to a preferred embodiment of the invention, the silicone gum corresponds to the following formula:in which:- R7, R8, R11 and R12 are identical or different, and each is chosen from alkyl radicals comprising from 1 to 6 carbon atoms,- R9 and R10 are identical or different, and each is chosen from an alkyl radical comprising from 1 to 6 carbon atoms, an aryl radical, a hydroxyl radical, a vinyl radical, preferably an alkyl radical comprising from 1 to 6 carbon atoms, a hydroxyl radical;- X is chosen from an alkyl radical comprising from 1 to 6 carbon atoms, a hydroxyl radical, a vinyl radical, preferably an alkyl radical comprising from 1 to 6 carbon atoms, a hydroxyl radical;- n and p are chosen so as to confer upon the silicone gum a molecular mass of greater than or equal to 400 000 g / mol.In general, n and p may each take values ranging from 0 to 5000, more particularly from 0 to 3000, knowing that n and p are not simultaneously zero.According to a particular embodiment, the silicone gum is a polydimethylsiloxane gum (INCI name Dimethicone), a polydimethylsiloxane gum comprising at least one aryl radical (INCI name: Diphenyl Dimethicone), a gum having the INCI name Dimethiconol, or mixtures thereof, and preferably a Dimethiconol gum.The silicone gum(s) can be used alone or as a mixture, in particular with a solvent chosen from the first oils and the second oils, described above, or mixtures thereof.The silicone gums may optionally be used in a form predissolved, for example, in a volatile or nonvolatile silicone oil which may or may not be identical to the second silicone oils detailed above. Usually, the proportion of gum represents from 5% to 20% by weight, and preferably from 10% to 15% by weight, in the silicone oil.Among the silicone gums that can be used within the context of the present invention, mention may be made of the Dimethicone gums (all the R and X radicals are methyl groups), sold under the names Silsoft SE 30 by the company Momentive Performance Materials, Belsil DM 500000 by the company Wacker. Among the Dimethiconol gums (the R radicals are methyl groups and the X radicals are hydroxyl groups), mention may be made of those sold under the names Xiameter® PMX-1401 Fluid (in cyclopentasiloxane), Xiameter PMX-1503 Fluid (in a Dimethicone), Xiameter® PMX-1403 Fluid (in a dimethicone) by the company Dow Corning, the products of the Mirasil D-DML-LV range sold by the company Elkem Silicones, Silsoft 1215 (in cyclopentasiloxane) by the company Momentive Performance Materials. As regards the gums of Diphenyl dimethicone type (R9and R10representing an aryl group, the other radicals R and X representing methyl groups), mention may for example be made of Mirasil C-DPDM (in cyclopentasiloxane) sold by the company Elkem Silicones.According to a preferred embodiment, the content of silicone gum, expressed as active material, ranges from 0.7% to 5% by weight, preferably from 1% to 2.5% by weight, relative to the total weight of the composition.ADDITIONAL NONVOLATILE HYDROCARBON OILSThe composition according to the invention may optionally comprise at least one additional polar or non-polar nonvolatile hydrocarbon oil.For the purposes of the invention, a "polar" oil comprises, in addition to carbon and hydrogen atoms, at least one oxygen or nitrogen atom, and preferably at least one oxygen atom.Polar nonvolatile hydrocarbon oilsAmong the polar nonvolatile hydrocarbon oils suitable for carrying out the invention, mention may be made of the oils more particularly chosen from:- C10-C26alcohols, preferably monohydroxy alcohols;- ethers of formula ROR’ or carbonates of formula RO(CO)OR’, in which formulae the groups R and R’, which may be identical or different, represent a saturated or unsaturated, branched or unbranched hydrocarbon group comprising at most 16 carbon atoms, preferably a C3-C16group;- nonvolatile hydrocarbon ester oils comprising one or more ester functions and comprising at least one linear or branched, saturated, unsaturated or aromatic hydrocarbon group, the total number of carbon atoms preferably being at least 12, and optionally one or more ether or hydroxyl functions;- mixtures thereof.The C10-C26alcohols are in particular chosen from lauryl alcohol, isostearyl alcohol, oleyl alcohol, 2-butyloctanol, 2-undecylpentadecanol, 2-hexyldecyl alcohol, isocetyl alcohol, octyldodecanol and mixtures thereof, and preferably octyldodecanol.Suitable ethers and carbonates may include, inter alia, dicaprylyl ether, dipropyl carbonate, diethylhexyl carbonate, dicaprylyl carbonate, C14-15 dialkyl carbonate.Among the suitable ester oils, mention may be made of monoesters and diesters optionally comprising one or two ether groups; linear or branched, saturated, unsaturated or aromatic triesters optionally comprising one to three ether groups; tetraesters; polyesters obtained by condensation of an unsaturated fatty acid dimer and / or trimer and of a diol; esters and polyesters of a monocarboxylic or dicarboxylic acid and of a dimer diol or of monoalcohols; plant oils, and also mixtures thereof.* Linear or branched, saturated, unsaturated or aromatic monoesters or diesters comprising more particularly from 12 to 80 carbon atoms and optionally comprising one or two ether groups. Mention may be made, among the compounds of this type, of monoesters or diesters obtained from a saturated or unsaturated monocarboxylic or dicarboxylic fatty acid, in particular comprising from 4 to 28 and preferably from 4 to 24 carbon atoms, optionally comprising at least one free hydroxyl, on the one hand, and from a saturated or unsaturated monoalcohol or polyol, comprising from 2 to 26 and in particular from 3 to 24 carbon atoms and from 1 to 6 hydroxyl groups, on the other hand; the number of carbon atoms being at least 12 and preferably at least 16. In addition, the ester can optionally comprise one or two ether groups and optionally one or two hydroxyl groups.By way of example, mention may be made of 2-octyldodecyl neopentanoate, isodecyl neopentanoate, isotridecyl neopentanoate, isostearyl neopentanoate, isostearyl heptanoate, cetostearyl octanoate, cetyl octanoate, tridecyl octanoate, isononyl isononanoate, isotridecyl isononanoate, octyl isononanoate, hexyl laurate, 2-hexyldecyl laurate, 2-ethylhexyl palmitate, isopropyl palmitate, ethyl palmitate, 2-octyldecyl palmitate, isopropyl myristate, 2-octyldodecyl myristate, isopropyl stearate, butyl stearate, octyl stearate, 2-octyldodecyl stearate, glyceryl stearate, isopropyl isostearate, isostearyl isostearate, isostearyl behenate, isocetyl stearate, mixtures of esters of capric acid, of caprylic acid and of a coconut-derived alcohol (C12-C18alcohols), 2-octyldodecyl erucate, oleyl erucate, isostearyl lactate, octyl hydroxystearate, octyldodecyl hydroxystearate, diisostearyl malate, isocetyl stearoyl stearate, diisostearyl adipate, or mixtures thereof.Mention may also be made of optionally hydroxylated esters of a C2-C8mono- or polycarboxylic acid and of a C2-C8alcohol. Suitable in particular for carrying out the invention are the monoesters of a C2-C8carboxylic acid and of a C2-C8alcohol, which are optionally hydroxylated, and the diesters of a C2-C8dicarboxylic acid and of a C2-C8alcohol, which are optionally hydroxylated, such as diisopropyl adipate, bis(2-ethylhexyl) adipate, dibutyl adipate or bis(2-ethylhexyl) succinate.Mention may also be made of linear or branched, saturated, unsaturated or aromatic esters of a saturated or unsaturated monocarboxylic acid, in particular comprising from 4 to 28 carbon atoms, and of diols, in particular glycols, especially of C2-C5, of glycerol or of polyglycerol. Mention may be made for example of propylene glycol monoisostearate, propylene glycol monoricinoleate, neopentyl glycol dicaprate, neopentyl glycol diheptanoate, propylene glycol dioctanoate, diethylene glycol diisononanoate, polyglyceryl-2 diisostearate, polyglyceryl-3 diisostearate, ethylene glycol dibenzoate, diethylene glycol dibenzoate, propylene glycol dibenzoate, dipropylene glycol dibenzoate and also mixtures thereof.* Linear or branched, saturated, unsaturated or aromatic triesters comprising up to 80 carbon atoms and optionally comprising one to three ether groups. Suitable for the invention are the esters obtained from linear or branched, saturated, unsaturated or aromatic, C2-C40, preferably C4-C40, mono- or polycarboxylic acids, which are optionally hydroxylated, and from C2-C40, preferably C3-C40, polyols or monoalcohols; said polyesters optionally comprising at least one free hydroxyl.Use may be made, for example, of triacetin and also triglycerides of saturated or unsaturated C4-C36fatty acids, more particularly saturated or unsaturated, linear or branched C8-C20fatty acids, such as, for example, triglycerides of heptanoic acid or octanoic acid; in particular, mention may be made of saturated triglycerides, such as Caprylic / Capric Triglyceride, for example such as the products sold under the DUB MCT range by Stéarinerie Dubois, glyceryl triheptanoate, glyceryl trioctanoate, triglycerides of C18-36acid, such as those sold under the reference DUB TGI 24 by Stéarinerie Dubois, or glyceryl triisostearate.Mention may also be made of triesters of glycerol or polyglycerol and of monocarboxylic acids, such as polyglycerol-2 triisostearate or glyceryl tri(2-decyltetradecanoate).Mention may also be made, by way of example, of oils comprising three ester functions, which are optionally hydroxylated or acetylated, of a C2-C9acid comprising three carboxyl functions, which is optionally hydroxylated, and of a C2-C20monoalcohol. Mention may be made of citric acid esters, such as, for example, triethyl citrate, trioctyl citrate, tributyl citrate, tributyl acetylcitrate and likewise tridecyl trimellitate, and also mixtures thereof.* Tetraesters comprising in particular from 35 to 80 carbon atoms, optionally comprising one to three ether groups, such as tetraesters of pentaerythritol or polyglycerol and of a monocarboxylic acid, for example such as pentaerythrityl tetrapelargonate, pentaerythrityl tetraisostearate, pentaerythrityl tetraisononanoate, polyglyceryl-2 tetraisostearate or pentaerythrityl tetra(2-decyltetradecanoate).* Polyesters obtained by condensation of 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 of dilinoleic acid and of 1,4-butanediol. Mention may in particular 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 Hailucent ISDA, having the INCI name Polyglyceryl-2 Isostearate / Dimer Dilinoleate Copolymer.* Esters of a dimer diol or of a polyol, and of a mono- and / or dicarboxylic acid. Mention may be made for example of esters of a dimer diol and of a fatty acid and esters of a dimer diol and of a dicarboxylic acid dimer, in particular which may be obtained from a dicarboxylic acid dimer derived in particular from the dimerization of an unsaturated, particularly C8to C34, particularly C12to C22, in particular C16to C20and more particularly C18, fatty acid, such as esters of dilinoleic diacids and of dilinoleic dimer diols, having the INCI name Dimer Dilinoleyl Dimer Dilinoleate, for instance those sold by the company Nippon Fine Chemical under the trade names Lusplan DD-DA5®and DD-DA7®.Also suitable are esters derived from the esterification of a polyol, of at least one monocarboxylic acid and of at least one dicarboxylic acid, as described in particular in patent US 7 317 068. The polyol comprises more particularly 2 to 20 carbon atoms and 2 to 8 hydroxyl groups, it preferably being pentaerythritol. More particularly, the monocarboxylic acid comprises 4 to 30 carbon atoms, more particularly 6 to 22 carbon atoms, such as preferably stearic acid, isostearic acid, caprylic acid, capric acid or combinations thereof; as regards the linear or branched, saturated, unsaturated or aromatic dicarboxylic acid, it comprises more particularly 4 to 10 carbon atoms, and is preferably adipic acid. By way of example, mention may be made of Pentaerythrityl Isostearate / Caprate / Caprylate / Adipate, sold in particular under the name Crodamol L by the company Croda, Pentaerythrityl Adipate / Caprate / Caprylate / Heptanoate sold under the name Lexfeel 700 EX-LO- MB by the company Inolex.* Plant oils such as for example castor oil, olive oil, coconut oil, jojoba oil, ximenia oil, pracaxi oil, coriander seed oil, macadamia oil, passionflower oil, argan oil, sesame oil, sunflower oil, grape seed oil, avocado oil,Rosa caninaoil, apricot kernel oil, linseed oil, sweet almond oil, cottonseed oil, soybean oil, rapeseed oil, peanut oil, kaya oil, marula oil, camelina oil,wheat germ oil, maize oil, maize germ oil, rice bran oil, alfalfa oil, poppy oil, pumpkin oil, marrow oil, hazelnut oil, blackcurrant oil, evening primrose oil, millet oil, barley oil, quinoa oil, rye oil, safflower oil, candlenut oil, meadowfoam oil, black cumin oil, buriti oil, sandalwood nut oil, babassu oil, the liquid fraction of shea butter, and the liquid fraction of cocoa butter, and also mixtures thereof.Preferably, an oil chosen from castor oil, olive oil, coconut oil, jojoba oil, ximenia oil, macadamia oil, sesame oil, sunflower oil, grape seed oil, avocado oil, apricot kernel oil, linseed oil, sweet almond oil, cottonseed oil, soybean oil, rapeseed oil, peanut oil, wheat germ oil, maize germ oil, rice bran oil, alfalfa oil, safflower oil, meadowfoam oil, the liquid fraction of shea butter, and the liquid fraction of cocoa butter, and also mixtures thereof, is selected.Preferably, the polar hydrocarbon oil(s) are chosen from:- plant oils, in particular those just listed;- optionally hydroxylated ester oils comprising from 1 to 4 ester functions, of which at least one of them, which is linear or branched, saturated, unsaturated or aromatic, comprises at least 12 carbon atoms;- mixtures thereof.More particularly, if the composition contains them, the content of additional polar nonvolatile hydrocarbon oil(s) is less than 5% by weight, more particularly less than 2% by weight, and more particularly still between 0.5% and 1.5% by weight, relative to the total weight of the composition.Preferably, the composition according to the invention does not comprise additional polar nonvolatile hydrocarbon oil(s).Non-polar nonvolatile hydrocarbon oilsMore particularly, the non-polar nonvolatile hydrocarbon oil, different from the first oil(s) mentioned above, may be chosen from linear or branched hydrocarbons of mineral, plant or synthetic origin such as, for example:- liquid paraffin,- squalane, in particular of plant origin,- isoeicosane,- mixtures of linear saturated hydrocarbons, more particularly the mixtures having the following INCI names, for example: C18-21 Alkane, C21-28 Alkane, such as for example the products Gemseal 60, Gemseal 120 sold by Total,- hydrogenated or non-hydrogenated polybutenes, such as for example the products of the Indopol range sold by the company Ineos Oligomers,- hydrogenated or non-hydrogenated polyisobutenes, such as for example the nonvolatile compounds of the Parleam® range sold by the company Nippon Oil & Fat,- hydrogenated or non-hydrogenated polydecenes, such as for example the nonvolatile compounds of the Silkflo range sold by the company Ineos, and Dekanex by the company IMCD,- and mixtures thereof.Preferably, if the composition comprises at least one additional hydrocarbon oil, the latter is rather chosen from non-polar oils, alone or as a mixture.More particularly, if the composition contains them, the content of additional non-polar nonvolatile hydrocarbon oil(s) is less than 5%, preferably less than 2% by weight, and more particularly still between 0.5% and 1.5% by weight, relative to the total weight of the composition.Preferably, the composition according to the invention does not comprise any additional oil(s).WAXESThe composition according to the invention may optionally comprise at least one wax chosen from polar or non-polar hydrocarbon waxes, or silicone waxes, and also mixtures thereof.For the purposes of the present invention, the term "wax" is understood to mean a lipophilic compound, which is solid at ambient temperature (25°C), with a reversible solid / liquid change of state, which has a melting point of greater than or equal to 30°C that may be up to 120°C.For the purposes of the invention, the melting point corresponds to the temperature of the most endothermic peak observed on thermal analysis (DSC) as described in the ISO 11357-3; 1999 standard. The melting point of the wax may be measured using a differential scanning calorimeter (DSC), for example the calorimeter sold under the name DSC Q2000 by the company TA Instruments with the TA Universal Analysis software.The measuring protocol is as follows:A sample of 5 mg of wax is placed in a crucible and subjected to a first temperature rise ranging from -20°C to 120°C, at a heating rate of 10°C / minute, is then cooled from 120°C to -20°C at a cooling rate of 10°C / minute and is lastly subjected to a second temperature rise ranging from -20°C to 120°C at a heating rate of 5°C / minute.During the second temperature rise, the melting point of the solid fatty substance is measured, which corresponds to the temperature of the most endothermic peak observed of the melting curve, representing the variation in the difference in power absorbed as a function of the temperature.The enthalpy of fusion of the wax (∆Hf), corresponding to the integral of the entire melting curve obtained, may also be measured. This enthalpy of fusion of the wax is the amount of energy required to cause the compound to change from the solid state to the liquid state. It is expressed in J / g.The waxes may be silicone waxes and, preferably, hydrocarbon waxes. They are also of plant, mineral, animal and / or synthetic origin.In particular, the waxes have a melting point preferably greater than or equal to 35°C and better still greater than or equal to 40°C.Non-polar hydrocarbon waxesFor the purposes of the present invention, the term "non-polar hydrocarbon wax" is understood to mean a wax constituted solely of carbon and hydrogen atoms and free of heteroatoms, such as for example N, O, Si, P, etc.As examples of non-polar waxes that are suitable for use in the invention, mention may in particular be made of hydrocarbon waxes, such as microcrystalline waxes, paraffin waxes, ozokerite, polymethylene waxes, polyethylene waxes, Fischer-Tropsch waxes (or also Synthetic Wax) and microwaxes, in particular polyethylene microwaxes.Polar hydrocarbon waxesFor the purposes of the present invention, the term "polar hydrocarbon wax" is understood to mean a wax of which the chemical structure is formed essentially of, or even is constituted of, carbon and hydrogen atoms, and which comprises at least one heteroatom more particularly chosen from oxygen, optionally nitrogen, or mixtures thereof. It may thus contain alcohol, ester, ether, carboxylic acid, amine and / or amide groups.A wax chosen from ester waxes and alcohol waxes is preferred as polar hydrocarbon wax.According to the invention, the term "ester wax" is understood to mean a wax comprising at least one ester function. The ester waxes may also be hydroxylated.According to the invention, the term "alcohol wax" is understood to mean a wax comprising at least one alcohol function, i.e. comprising at least one free hydroxyl (OH) group.Use may notably be made, as ester wax, alone or as mixtures, of:i) waxes of formula R1COOR2in which R1and R2represent linear, branched or cyclic aliphatic chains, the number of atoms of which ranges from 6 to 50, in particular from 10 to 50, which may contain a heteroatom, such as for example O or N, and the melting point of which ranges more particularly from 30 to 120°C. In particular, use may be made, as ester wax, of a C20-C40alkyl (hydroxystearyloxy)stearate (the alkyl group comprising from 20 to 40 carbon atoms), alone or as a mixture, or a C20-C40alkyl stearate. Such waxes are notably sold under the names Kester Wax K 82 P®, Hydroxypolyester K 82 P®, Kester Wax K 80 P®or Kester Wax K82H by the company Koster Keunen. Use may also be made of stearyl heptanoate and stearyl caprylate and mixtures thereof.ii) bis(1,1,1-trimethylolpropane) tetrastearate,iii) diester waxes of a dicarboxylic acid of general formulaR3-(-OCO-R4-COO-R5), in which R3and R5are identical or different, preferably identical, and represent a C4-C30alkyl group and R4represents a linear or branched aliphatic C4-C30group which may or may not contain one or more unsaturations. Preferably, the C4-C30aliphatic group is linear and unsaturated.iv) mention may also be made of the waxes obtained by catalytic hydrogenation of animal or plant oils in particular containing linear or branched C8-C32fatty chains, such as for example hydrogenated jojoba oil, hydrogenated sunflower oil, hydrogenated castor oil or hydrogenated coconut kernel oil, and also the waxes obtained by hydrogenation of castor oil esterified with cetyl alcohol, such as those sold in the Phytowax Castor range, for example Phytowax Castor 22L73®, or else the waxes obtained by hydrogenation of olive oil esterified with stearyl alcohol, such as those of the Phytowax Olive range, for example Phytowax Olive 18L57, sold by the company Sophim. Such waxes are notably described in patent application FR2792190.v) waxes corresponding to the partial or total esters, preferably total esters, of a saturated, optionally hydroxylated, C16-C30carboxylic acid with glycerol. The term "total esters" is understood to mean that all the hydroxyl functions of the glycerol are esterified. Examples that may be mentioned include trihydroxystearin (or glyceryl trihydroxystearate), tristearin (or glyceryl tristearate) and tribehenin (or glyceryl tribehenate), alone or as a mixture. Among the suitable compounds, mention may be made of triesters of glycerol and of 12-hydroxystearic acid, or hydrogenated castor oil, such as for example Thixcin R and Thixcin E sold by Elementis Specialties.vi) mention may also be made of waxes of animal or plant origin, such as beeswax, synthetic beeswax, carnauba wax, candelilla wax, rice bran wax, ouricury wax, esparto grass wax, cork fibre wax, sugar cane wax, Japan wax, sumac wax, montan wax, orange wax, laurel wax, or sunflower wax, in particular refined sunflower wax.vii) mention may also be made of natural or synthetic polyoxyalkylenated or polyglycerolated hydrocarbon waxes, of animal or plant origin; the number of (C2-C4) oxyalkylene units may range from 2 to 100, the number of glycerol units may range from 1 to 20. Examples that may be mentioned include polyoxyethylenated beeswaxes, such as PEG-6 beeswax or PEG-8 beeswax; polyoxyethylenated carnauba waxes, such as PEG-12 carnauba; polyoxyethylenated or polyoxypropylenated and hydrogenated or non-hydrogenated lanolin waxes, such as PEG-30 lanolin or PEG-75 lanolin; PPG-5 lanolin wax glyceride; polyglycerolated beeswaxes, in particular polyglyceryl-3 beeswax, thewaxbased on Acacia Decurrens / Jojoba / Sunflower Seed Wax / Polyglyceryl-3 Esters, such as for example the product Acticire from the company Gattefossé.Silicone waxesThe term "silicone wax" is understood to mean a wax comprising at least one silicon atom, and in particular comprising Si-O groups.As silicone wax, mention may for example be made of C30-45 Alkyldimethylsilyl Polypropylsilsesquioxane (INCI name), sold for example under the names Dowsil SW-8005 C30 Resin Wax, Dowsil AMS-C30 Cosmetic Wax (as a mixture with C30-45 Olefin), by the company Dow Corning. Such waxes are described in particular in patent application WO2005 / 100444. Mention may also be made of siliconized beeswax, such as for example Polyglyceryl-3 Beeswax.Preferably, the composition comprises at least one wax, more particularly chosen from the silicone waxes. Advantageously, the composition comprises, as wax, a silicone wax, preferably the wax C30-45 Alkyldimethylsilyl Polypropylsilsesquioxane.Preferably, the content of wax(es) advantageously ranges from 1% to 5% by weight, in particular from 1.5% to 3.5% by weight, relative to the total weight of the composition.PIGMENTSThe composition according to the invention additionally comprises at least 8 % by weight, preferably at least 10% by weight, relative to the total weight of the composition, of at least one pigment.The term "pigments" is understood to mean white or coloured, mineral or organic particles, which are insoluble in the composition, and which are intended to colour the resulting composition and / or deposit.According to a particular embodiment, the pigments used according to the invention are chosen from mineral pigments.The term "mineral pigment" is understood to mean any pigment which corresponds to the definition of Ullmann's Encyclopedia in the chapter on inorganic pigments. Mention may be made, among the mineral pigments of use in the present invention, of zirconium oxide or cerium oxide, and also zinc oxide, iron oxide (black, yellow or red) or chromium oxide, manganese violet, ultramarine blue, chromium hydrate and ferric blue, titanium dioxide and metal powders, such as aluminium powder and copper powder. The following mineral pigments may also be used: Ta2O5, Ti3O5, Ti2O3, TiO, ZrO2as a mixture with TiO2, ZrO2, Nb2O5, CeO2, ZnS.The size of the pigment that is of use in the context of the present invention is generally greater than 100 nm and may range up to 10 µm, preferably from 200 nm to 5 µm and more preferentially from 300 nm to 1 µm. According to one particular form of the invention, the pigments have a size characterized by a D

[0050] of greater than 100 nm and possibly ranging up to 10 µm, preferably from 200 nm to 5 µm and more preferentially from 300 nm to 1 µm. The sizes are measured by laser diffraction using a commercial MasterSizer 3000® particle size analyser from Malvern, which makes it possible to determine the particle size distribution of all of the particles over a wide range that may extend from 0.01 µm to 1000 µm. The data are processed on the basis of the conventional Mie scattering theory. This theory is the most suitable for size distributions ranging from submicron to multimicron; it allows an "effective" particle diameter to be determined. This theory is in particular described in the publication by Van de Hulst, H.C., Light Scattering by Small Particles, Chapters 9 and 10, Wiley, New York, 1957. D

[0050] represents the maximum size exhibited by 50% by volume of the particles.In the context of the present invention, the mineral pigments are more particularly iron oxide and / or titanium dioxide. Examples that may be mentioned more particularly include titanium dioxides and iron oxide coated with aluminium stearoyl glutamate, sold, for example, under the reference NAI® by the company Miyoshi Kasei.As mineral pigments that may be used in the invention, mention may also be made of pearlescent agents.The term "pearlescent agents" should be understood as meaning coloured particles of any shape, which are or are not iridescent, in particular produced by certain molluscs in their shells or else synthesized, and which exhibit a colour effect by optical interference.The pearlescent agents may be chosen from pearlescent pigments such as titanium oxide-coated mica covered with an iron oxide, titanium oxide-coated mica covered with bismuth oxychloride, titanium oxide-coated mica covered with chromium oxide, titanium oxide-coated mica covered with an organic dye and also pearlescent 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 colorants.Examples of pearlescent agents that may also be mentioned include natural mica covered with titanium oxide, with iron oxide, with natural pigment or with bismuth oxychloride.The pearlescent agents may more particularly have a yellow, pink, red, bronze, orangey, brown, gold and / or coppery colour or tint.Among the pigments that may be used according to the invention, mention may also be made of those having an optical effect other than a simple conventional colouring effect, i.e. a unified and stabilized effect such as produced by conventional colorants, for instance monochromatic pigments.For the purposes of the invention, the term "stabilized" means lacking the effect of variability of the colour with the angle of observation or in response to a temperature change.For example, this material may be chosen from particles with a metallic tint, goniochromatic colouring agents, diffractive pigments, thermochromic agents, optical brighteners, and also fibres, in particular interference fibres. Needless to say, these various materials may be combined in order simultaneously to afford two effects, or even a novel effect in accordance with the invention.According to one particular embodiment, the composition according to the invention comprises at least one uncoated pigment.According to another particular embodiment, the composition according to the invention comprises at least one pigment coated with at least one lipophilic or hydrophobic compound. This type of pigment is particularly advantageous. In so far as they are treated with a hydrophobic compound, they show predominant affinity for an oily phase, which can then carry them. The coating may also comprise at least one additional non-lipophilic compound.For the purposes of the invention, the "coating" of a pigment according to the invention generally denotes the total or partial surface treatment of the pigment with a surface agent, absorbed, adsorbed or grafted onto said pigment.The surface-treated pigments may be prepared according to surface treatment techniques of chemical, electronic, mechanochemical or mechanical nature that are well known to a person skilled in the art. Commercial products may also be used.The surface agent may be absorbed, adsorbed or grafted onto the pigments by evaporation of solvent, chemical reaction and creation of a covalent bond. According to one variant, the surface treatment consists in coating the pigments. The coating may represent from 0.1% to 20% by weight and in particular from 0.5% to 5% by weight, of the total weight of the coated pigment.The coating may be produced, for example, by adsorption of a liquid surface agent onto the surface of the solid particles by simple mixing with stirring of the particles and of said surface agent, optionally with heating, prior to the incorporation of the particles into the other ingredients of the makeup or care composition.The coating may be produced, for example, by chemical reaction of a surface agent with the surface of the solid pigment particles and creation of a covalent bond between the surface agent and the particles. This method is notably described in patent US 4 578 266.The chemical surface treatment can consist in diluting the surface agent in a volatile solvent, dispersing the pigments in this mixture and then slowly evaporating off the volatile solvent, so that the surface agent is deposited on the surface of the pigments.According to one particular embodiment of the invention, the pigments may be coated according to the invention with at least one compound chosen from silicone surface agents; fluoro surface agents; fluorosilicone surface agents; metal soaps; N-acylamino acids or salts thereof; lecithin and derivatives thereof; isopropyl triisostearyl titanate; isostearyl sebacate; natural plant or animal waxes; polar synthetic waxes; fatty esters; phospholipids; and mixtures thereof.According to one particular embodiment, the colorant is an organic pigment, which is synthetic, natural or of natural origin.The term "organic pigment" is understood to mean any pigment that satisfies the definition in Ullmann's Encyclopedia in the chapter on organic pigments. The organic pigment may in particular be chosen from nitroso, nitro, azo, xanthene, quinoline, anthraquinone, phthalocyanine, metal-complex type, isoindolinone, isoindoline, quinacridone, perinone, perylene, diketopyrrolopyrrole, thioindigo, dioxazine, triphenylmethane or quinophthalone compounds.The organic pigment(s) may be chosen, for example, from carmine, carbon black, aniline black, melanin, azo yellow, quinacridone, phthalocyanine blue, sorghum red, the blue pigments codified in the Color Index under the references CI 42090, 69800, 69825, 73000, 74100 and 74160, the yellow pigments codified in the Color Index under the references CI 11680, 11710, 15985, 19140, 20040, 21100, 21108, 47000 and 47005, the green pigments codified in the Color Index under the references CI 61565, 61570 and 74260, the orange pigments codified in the Color Index under the references CI 11725, 15510, 45370 and 71105, the red pigments codified in the Color Index under the references CI 12085, 12120, 12370, 12420, 12490, 14700, 15525, 15580, 15620, 15630, 15800, 15850, 15865, 15880, 17200, 26100, 45380, 45410, 58000, 73360, 73915 and 75470, and the pigments obtained by oxidative polymerization of indole or phenol derivatives as described in patent FR 2 679 771.The pigments may also be in the form of composite pigments as described in patent EP 1 184 426. These composite pigments may be composed in particular of particles comprising an inorganic core at least partially covered with an organic pigment and at least one binder providing the fixing of the organic pigments to the core.The pigment may also be a lake.The term "lake" is understood to mean insolubilized dyes adsorbed on insoluble particles, the assembly thus obtained remaining insoluble during use.The inorganic substrates onto which the dyes are adsorbed are, for example, alumina, silica, calcium sodium borosilicate or calcium aluminium borosilicate, and aluminium.Mention may be made, among the organic dyes, of cochineal carmine. Mention may also be made of the products known under the following names: D&C Red 21 (CI 45 380), D&C Orange 5 (CI 45 370), D&C Red 27 (CI 45 410), D&C Orange 10 (CI 45 425), D&C Red 3 (CI 45 430), D&C Red 4 (CI 15 510), D&C Red 33 (CI 17 200), D&C Yellow 5 (CI 19 140), D&C Yellow 6 (CI 15 985), D&C Green (CI 61 570), D&C Yellow 1 O (CI 77 002), D&C Green 3 (CI 42 053), D&C Blue 1 (CI 42 090). Mention may be made, as examples of lakes, of the product known under the name D&C Red 7 (CI 15 850:1).More particularly, the content of pigment(s) is at least 8% by weight, preferably at least 10% by weight, and advantageously represents from 8% to 15% by weight, preferably from 10% to 14% by weight, relative to the total weight of the composition.As indicated above, the (silicone resin + silicone polyamide) / pigment(s) weight ratio is between 1 and 2.7, preferably between 1 and 2.5.LIPOPHILIC THICKENERThe composition according to the invention may also comprise at least one lipophilic thickener chosen more particularly from silicas which may or may not be hydrophobically treated; lipophilic clays, alone or as a mixture, and preferably silica which may or may not be hydrophobically treated.SilicasThe composition according to the invention may thus comprise, as lipophilic thickener, a fumed silica, preferably a hydrophobic fumed silica, or silica aerogel particles, preferably hydrophobic silica aerogel particles.a) Fumed silicaFumed silica which has been hydrophobically surface treated is suitable for use in the invention. It is in fact possible to chemically modify the surface of the silica, by chemical reaction generating a reduction in the number of silanol groups present at the surface of the silica. It is possible in particular to substitute silanol groups with hydrophobic groups: a hydrophobic silica is then obtained.The hydrophobic groups may be:- trimethylsiloxyl groups, which are obtained in particular by treatment of fumed silica in the presence of hexamethyldisilazane. Silicas thus treated are known as "Silica Silylate" according to the CTFA (8th edition, 2000). They are sold, for example, under the references Aerosil R812® by the company Degussa, and Cab-O-Sil TS-530® by the company Cabot.- dimethylsilyloxyl or polydimethylsiloxane groups, which are obtained in particular by treating fumed silica in the presence of polydimethylsiloxane or dimethyldichlorosilane. Silicas thus treated are known as "Silica Dimethyl Silylate" according to the CTFA (8th edition, 2000). They are sold, for example, 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.b) Silica aerogelsSilica aerogels are porous materials obtained by replacing (by drying) the liquid component of a silica gel with air.They are generally synthesized via a sol-gel process in a liquid medium and then dried, usually by extraction with a supercritical fluid, the one most commonly used being supercritical CO2. 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 operations are described in detail in Brinker C.J. and Scherer G.W., Sol-Gel Science, New York, Academic Press, 1990.The hydrophobic silica aerogel particles usually have a specific surface area per unit mass (SM) ranging from 500 to 1500 m2 / g, preferably from 600 to 1200 m2 / g and better still from 600 to 800 m2 / g, and a size expressed as the volume-average diameter (D[0.5]) ranging from 1 to 1500 µm, better still from 1 to 1000 µm, preferably from 1 to 100 µm, in particular from 1 to 30 µm, more preferably from 5 to 25 µm, better still from 5 to 20 µm and even better still from 5 to 15 µm.According to one embodiment, the hydrophobic silica aerogel particles used in the present invention have a size expressed as volume-average diameter (D[0.5]) ranging from 1 to 30 µm, preferably from 5 to 25 µm, better still from 5 to 20 µm and even better still from 5 to 15 µm.The specific surface area per unit mass may be determined by the nitrogen absorption method, known as the BET (Brunauer-Emmett-Teller) method, described in the Journal of the American Chemical Society, vol. 60, page 309, February 1938 and corresponding to international standard ISO 5794 / 1 (annex D). The BET specific surface area corresponds to the total specific surface area of the particles under consideration.The sizes of the silica aerogel particles may be measured by static light scattering using a commercial MasterSizer 2000 particle size analyser 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 in particular described in the publication by Van de Hulst, H.C., Light Scattering by Small Particles, Chapters 9 and 10, Wiley, New York, 1957.According to one advantageous embodiment, the hydrophobic silica aerogel particles used in the present invention have a specific surface area per unit mass (SM) ranging from 600 to 800 m2 / g and a size expressed as the volume-average diameter (D[0.5]) ranging from 5 to 20 µm and even better still from 5 to 15 µm.The aerogels are aerogels of hydrophobic silica, preferably of silylated silica (INCI name: Silica Silylate).The term "hydrophobic silica" is understood to mean any silica of which the surface is treated with silylating agents, for example with 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.As regards the preparation of hydrophobic silica aerogel particles that have been surface-modified by silylation, reference may be made to the document US 7 470 725.Use will preferably be made of hydrophobic silica aerogel particles surface-modified with trimethylsilyl groups.As hydrophobic silica aerogels 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 an average size of about 1000 microns and a specific surface area per unit mass ranging from 600 to 800 m2 / g.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, Enova® Aerogel MT 1100 and Enova Aerogel MT 1200.Use will preferably be made of the aerogel sold under the name VM-2270 (INCI name: Silica Silylate) by the company Dow Corning, the particles of which have an average size ranging from 5-15 microns and a specific surface area per unit mass ranging from 600 to 800 m2 / g.Lipophilic claysThe lipophilic thickener that may be used within the context of the present invention may also be a lipophilic clay.The term "lipophilic clay" is understood to mean any clay that is liposoluble or lipodispersible in an oily phase.The term "clay" more particularly denotes a material based on hydrated silicates and / or aluminosilicates of lamellar structure.The clays may be natural or synthetic. Mention may be made, as examples of such products, of clays of the family of the smectites, and also of the family of the vermiculites, stevensite or chlorites. These clays may be of natural or synthetic origin.Preferably, use is made of organophilic clays, more particularly of modified clays, such as montmorillonite, bentonite, hectorite, attapulgite or sepiolite, and mixtures thereof. The clay is preferably a bentonite or a hectorite.More particularly, the clays are made lipophilic by treatment with an alkylammonium salt such as an ammonium halide, such as, for example, a C10 to C22 ammonium chloride, possibly comprising an aromatic group. In particular, mention may be made of halides, such as stearalkonium, benzalkonium or dialkyldimethylammonium, for example distearyldimethylammonium, chlorides.The lipophilic clay may be present in the form of a powder or in a form that is predispersed in a solvent chosen, for example, from C1-C2 alcohols, such as methanol, ethanol; propylene carbonate, triethyl citrate, and mixtures thereof.The lipophilic clay suitable for carrying out the invention may be chosen from the modified hectorites having the following INCI names: Disteardimonium hectorite, Stearalkonium Hectorites, Quaternium-18 Hectorite, alone or as mixtures. Preferably, the composition comprises Disteardimonium hectorite.The lipophilic bentonite suitable for carrying out the invention may be chosen from the bentonites having the following INCI names: Quaternium-18 bentonites, Stearalkonium Bentonites, Quaternium-18 / Benzalkonium Bentonite, alone or as mixtures.Among the modified hectorites that may be used in the context of the invention, mention may be made of:*among the Disteardimonium Hectorites: Bentone 38V, Bentone 38V CG, Bentone Gels;*among the Stearalkonium Hectorites: Bentone 27V; sold by the company Elementis Specialties.Among the modified bentonites that may be used in the context of the invention, mention may be made, alone or as mixtures, of:*among the quaternium-18 bentonites: Bentone 34 sold by the company Elementis Specialties; Claytone 40, Tixogel VP sold by the company BYK Additives Inc;*among the Stearalkonium Bentonites: Tixogel VZ, Claytone AF, Claytone APA sold by the company BYK Additives Inc;*among the Quaternium-18 / Benzalkonium Bentonites: Claytone HT sold by the company BYK Additives Inc.According to a preferred embodiment, the lipophilic clay filler comprising at least one quaternary ammonium group is chosen from lipophilic hectorites, in particular Disteardimonium Hectorite.Preferably, the composition according to the invention comprises at least one lipophilic thickener chosen from silica, preferably hydrophobically treated silica.More particularly, if the composition comprises any, the content of lipophilic thickener represents from 0.2% to 3% by weight, preferably from 0.5% to 1.5% by weight, relative to the total weight of the composition.WATERThe composition according to the invention may optionally comprise water. Preferably, if the composition comprises any, the water content does not exceed 5% by weight, preferably does not exceed 3% by weight, relative to the total weight of the composition. Even more advantageously, the water content, if the composition comprises any, does not exceed 2% by weight, in particular does not exceed 1% by weight and more particularly still does not exceed 0.5% by weight, relative to the total weight of the composition.FILLERSThe composition according to the invention may comprise at least one mineral or organic filler. It should be noted that the fillers, in particular the mineral fillers, are chosen from compounds different from the abovementioned lipophilic thickeners.The term "mineral filler" is understood to mean any compound in which the chemical structure does not comprise a carbon atom, independently of the presence of a coating of said filler.For the purposes of the invention, the term "organic filler" is understood to mean solid particles of at least one hydrocarbon, or silicone compound, or combinations thereof, independently of their coating.The fillers are in the form of particles and are distinct from the pigments described above.The fillers used in the compositions according to the present invention may be particles in lamellar, globular or spherical form, in the form of fibres or in any other form intermediate between these defined forms. The fillers can be spherical, that is to say comprise at least a rounded general portion, in particular defining at least a sphere portion, preferably internally defining a concavity or a hollow (sphere, globules, bowls, horseshoe, etc.), or lamellar.In accordance with a particular embodiment of the invention, the fillers more particularly have an average particle size (expressed as volume-average diameter - D[0.5]) of at least 1 µm, preferably of at least 2 µm, advantageously of between 2 and 15 µm. The size of the particles can be measured by laser diffraction using a commercial Mastersizer 3000 particle size analyser from the company Malvern (see also the standard ISO 13320).The fillers used in the composition according to the invention may or may not be surface coated, and in particular they may be coated with a hydrophobic treatment agent, in particular promoting the dispersion and compatibility of the filler in the composition. The hydrophobic treatment agent may be chosen from silicones, in particular silanes; fluorinated derivatives, fatty acids such as stearic acid; metal soaps such as aluminium dimyristate, the aluminium salt of hydrogenated tallow glutamate; amino acids; N-acylamino acids or salts thereof; lecithin, isopropyl triisostearyl titanate, and mixtures thereof. The N-acylamino acids may comprise an acyl group having from 8 to 22 carbon atoms, such as, for example, a 2-ethylhexanoyl, caproyl, lauroyl, myristoyl, palmitoyl, stearoyl or cocoyl group. The salts of these compounds may be the aluminium, magnesium, calcium, zirconium, zinc, sodium or potassium salts. The amino acid may be, for example, lysine, glutamic acid or alanine. The term "alkyl" mentioned in the compounds cited above in particular denotes an alkyl group having from 1 to 30 carbon atoms and preferably having from 5 to 16 carbon atoms.As examples of mineral fillers, mention may be made of:- silica (INCI name: Silica), preferably in the form of spherical particles, such as the porous silica microspheres sold under the name Silica Beads SB-700 by the company Myoshi; "Sunsphere H51" and "Sunsphere H33" by the company Asahi Glass; the polydimethylsiloxane-coated amorphous silica microspheres sold under the name "SA Sunsphere H33" and "SA Sunsphere H53" by the company Asahi Glass; hollow silica microspheres.- perlite, such as those sold by the company World Minerals under the trade name Perlite P1430, Perlite P2550, Perlite P2040, OpTiMatTM 1430 OR or 2550 OR. Europerl EMP-2 and Europerl 1 by the company Imerys.- zeolites such as the products sold by the company Zeochem under the names ZeoFlair 300, Zeoflair 200, Zeoflair 100, X-MOL and X-MOL MT.- calcium magnesium carbonate particles, such as those sold by the company Imerys under the name Calcidol, by the company LCW (Sensient) under the name Carbomat or by the company Omya under the name Omyacare S60-AV. Calcium carbonate, magnesium carbonate, magnesium hydrogen carbonate and hydroxyapatite are also suitable.- particles of kaolin or talc, for example sold under the Imercare, Imercare Pharma and Luzenac Pharma ranges by the company Imerys; Rose Talc by the company Nippon Talc.- natural or synthetic mica, such as the product with the INCI name Synthetic Fluorphlogopite, sold under the names RonaFlair Silk Mica by the company Merck, Sericite PHN by the company Presperse, NHS-100 and NHS-150 by the company Myoshi Kasei, those sold under the names PDM-NSO or FNK-100 by the company Topy.- boron nitride; composites of silica and titanium dioxide, such as the TSG® series sold by Nippon Sheet Glass; bismuth oxychloride.- glass or ceramic microcapsules; for example, borosilicate particles.- mixtures thereof.If the composition comprises any, the content of mineral filler(s) represents from 0.5% to 4% by weight, preferably from 1% to 3% by weight, relative to the total weight of the composition.Among the suitable organic fillers, mention may in particular be made of:- natural or synthetic micronized waxes.- metal soaps derived from organic carboxylic acids having from 8 to 22 carbon atoms, preferably from 12 to 18 carbon atoms, for example zinc, magnesium or lithium stearate, zinc laurate, magnesium myristate.- natural organic materials such as polysaccharide powders, and in particular starch powders, especially crosslinked or non-crosslinked maize, wheat or rice starch powders, powders of starch crosslinked with octenylsuccinic anhydride sold under the name Dry-Flo® by the company National Starch or powders of waxy maize starch, such as those which are sold under the names C* Gel 04201 by the company Cargill, Corn Starch B by the company Roquette and Organic Corn Starch by the company Draco Natural Products.- cellulose, in particular in the form of spherical particles, such as products of the Cellulobeads D-10, Cellulobeads D-5 and Cellulobeads USF type sold by the company Daito Kasei Kogyo.- N-(C8-C22 acyl)amino acids; the amino acid can, for example, be lysine, glutamic acid or alanine, preferably lysine. Mention may be made, for example, of lauroyl lysine sold in particular under the names Amihope LL by the company Ajinomoto or Corum 5105 by the company Corum.- particles of acrylic (co)polymers and derivatives thereof, in particular:* of polymethyl methacrylate (INCI name Methyl Methacrylate Crosspolymer) sold under the name Covabead LH85 by the company Sensient, or Polymethyl Methacrylate under the names Sepimat P by the company SEPPIC and Microsphere M-100® by the company Matsumoto Yushi-Seiyaku;* of polymethyl methacrylate / ethylene glycol dimethacrylate (INCI name Methyl Methacrylate / Glycol Dimethacrylate Crosspolymer) sold under the name Dow Corning 5640 Microsponge Skin Oil Adsorber by the company Dow Corning;* of crosslinked acrylate (INCI name: Acrylates Crosspolymer) sold for example under the name Ganzpearl GMP-0820 by the company Ganz Chemical;* of polyallyl methacrylate / ethylene glycol dimethacrylate sold under the name Poly-Pore L200 or Poly-Pore E200 by the company Amcol Health and Beauty Solutions Inc.;* of ethylene glycol dimethacrylate / lauryl methacrylate copolymer (INCI name: Lauryl Methacrylate / Glycol Dimethacrylate Crosspolymer) sold under the name Polytrap 6603 Adsorber by the company Amcol Health and Beauty Solutions Inc.;* of crosslinked acrylate / alkyl acrylate copolymer (INCI name: Acrylates / Ethylhexyl Acrylate Crosspolymer) sold under the name Techpolymer ACP-8C by the company Sekisui Plastics;* of ethylene / acrylate copolymer, such as that sold under the name Flobeads® by the company Sumitomo Seika Chemicals.- particles of acrylonitrile (co)polymer, in particular the expanded hollow particles sold under the name Expancel by the company Akzo Nobel, or the microspheres sold under the name Micropearl F 80 ED® by the company Matsumoto.- polyurethane particles, for example sold under the names D-400, D-800 (INCI name: HDI / Trimethylol Hexyllactone Crosspolymer (and) Silica), CS-400 (INCI name: HDI / PPG / Polycaprolactone Crosspolymer (and) Silica), by the company Toshiki.- silicone polymer particles, advantageously chosen from:* silicone resin particles such as those having the INCI name Polymethylsilsesquioxane sold in particular under the name Tospearl, in particular Tospearl 145 A, by the company Momentive Performance Materials;* silicone elastomer particles coated with silicone resin, in particular with silsesquioxane resin, such as the products sold under the names KSP-100, KSP-101, KSP-102, KSP-103, KSP-104, KSP-105 (INCI name: Vinyl Dimethicone / Methicone Silsesquioxane Crosspolymer), or KSP-300 (INCI name: Diphenyl Dimethicone / Vinyl Diphenyl Dimethicone / Silsesquioxane Crosspolymer) by the company Shin Etsu;* silicone elastomer particles such as the products sold under the name Dowsil 9506 Cosmetic Powder by the company Dow Corning (INCI name: Dimethicone / Vinyl Dimethicone Crosspolymer);* Methylsilanol / Silicate Crosspolymer particles, for example in the form of bowls, such as those sold in particular under the name TAK-110 by the company Takemoto Oil & Fat.- polyamide particles, such as Nylon®, in particular Nylon 12, Nylon 6 / 12; such as the nylon powders sold under the names Orgasol 2002 EXS NAT COS, Orgasol 4000 EXD NAT COS Caresse, by the company Arkema.- particles of tetrafluoroethylene polymers (Teflon®).Preferably, if the composition comprises any, the organic filler may be chosen from cellulose particles, particles of N-(C8-C22 acyl)amino acids, such as lauroyl lysine, and also mixtures thereof.In accordance with a particular embodiment of the invention, the content of organic filler(s) represents from 0.5% to 5% by weight, preferably from 1% to 3% by weight, relative to the total weight of the composition.According to a particularly advantageous embodiment of the present invention, it may be that the composition does not comprise polymeric organic fillers, considered to be microplastics. It will be recalled that, for the purposes of the invention, the term "microplastics" means solid particles, having a stable shape, of polymer comprising carbon atoms in the polymer chain (backbone), of synthetic origin or of chemically modified natural origin, insoluble in water (i.e.: less than 2 g / l; OECD Directive 105), with a size less than 5 mm (and with a size less than 15 mm for fibres). The term "stable form" denotes particles remaining solid in the composition and after its use. For example, polymer particles forming a film in the composition or when said composition is used are not considered to be of stable form. Thus, preferably, it may be that the composition according to the invention does not comprise particles of acrylic polymers or copolymers, acrylonitriles, polyurethanes, polyamides, tetrafluoroethylene polymers, silicone polymers, as described above. If, however, the composition were to comprise any, their content would preferably be less than 5% by weight, more particularly less than 2% by weight and advantageously less than 1% by weight, relative to the total weight of the composition. Preferably, if the composition comprises any, the content of organic filler(s) of the aforementioned microplastics type is less than or equal to 0.01% by weight, relative to the total weight of the composition, and very advantageously, the composition is devoid of organic fillers.Preferably, the composition may optionally comprise at least one mineral filler chosen from kaolin, mica and optionally silica different from the lipophilic thickeners, and mixtures thereof. The composition may also comprise at least one organic filler, particularly cellulose, N-(C8-C22 acyl)amino acids, lauroyl lysine, and mixtures thereof.OPTIONAL ADJUVANTSIn the context of the present invention, the composition may also contain at least one optional adjuvant chosen from those usually used in the cosmetics field, in particular for compositions for making up and / or caring for the skin and the lips.By way of examples, mention may be made of preservatives; antioxidants; thickeners other than those listed above or other than the waxes mentioned above; complexing agents; solvents; active agents; fragrances; etc.Of course, a person skilled in the art will take care to choose the optional additional additives and / or the amount thereof such that the advantageous properties of the compositions according to the invention are not, or are not substantially, adversely affected by the envisaged addition.The invention also relates to a process for making up and / or caring for the skin and / or the lips, in particular the lips, in which the composition according to the invention is applied.It is also pointed out that the compositions according to the invention more particularly comprise a cosmetically (or physiologically) acceptable medium, i.e. one which has a pleasant colour, odour and feel and which does not give rise to any unacceptable discomfort, i.e. stinging, tautness or redness, that is liable to discourage the user from applying such compositions.Throughout the description, including the claims, the expression "comprising a" should be understood as being synonymous with "comprising at least one", unless otherwise specified.The expressions "between ... and ..." and "ranging from ... to ..." should be understood as meaning limits included, unless otherwise specified.In addition, the sum of the amounts of the ingredients of the composition represents 100% by weight of the composition.The invention is illustrated in greater detail by the examples presented below.The starting materials are referred to by their chemical or INCI name.EXAMPLESProtocol for measuring the viscosityThe viscosity measurement is performed with a sample of the composition at 25°C, one to three days after production thereof (storage at ambient temperature), using a Rheomat RM 180 viscometer equipped with a No. 2 or 3 spindle, the measurement being performed after 10 minutes of rotation of the spindle within the formulation at a shear rate of 200 revolutions / min (rpm).Protocol for measuring the tackThe composition is deposited on several stainless steel dishes with a depth of 100 μm and levelled as quickly as possible. The dishes are left to dry at ambient temperature for one hour.The apparatus used is a TAXT2i texture analyser. The clamp mounted on the apparatus grips an AU4G cylinder with a diameter of 6 mm, at the end of which is adhesively bonded a smooth beige synthetic skin end piece of the same diameter and with a thickness of 2 mm.The end piece is cleaned with ethanol between each measurement.More than one measurement is never taken at the same place in the deposit.The parameters of the compression tests with holding over time are indicated below:Approach speed(or pre-speed)1 mm / sSpeed(from detection of contact)0.1 mm / sForce(and corresponding pressure)0.283 N (i.e. 0.01 MPa)Holding time3 sWithdrawal speed(or post-speed)0.1 mm / sThe tack is characterized by the work of detachment measured during the unloading (tensile phase), corresponding to the integral of the curve under the time axis. This work is expressed positively in joules per square metre.Protocol for measuring the transfer1. Preparation of the test:Support:Beige Supplale (2.5 x 5 cm) (sold by Soudotique).Spread composition (D) over the entire surface three times in a row to obtain a homogeneous deposit. Repeat the operation on two other strips.Allow the deposit to dry on a plate heated to 34°C for 30 minutes.If necessary, take a photo of each support with the deposit (made up) before stressing.2. Stresses:Preparation of a paper tissue for each stress:Fold each paper tissue twice along the long edge and then twice in the other direction to form a square.Dry resistance:Rub once with the folded tissue lengthwise against one of the three made-up supports; the force applied is that normally exerted when removing makeup from the skin or the lips.Observe the state of the rubbed support and the used surface of the tissue, in particular the remaining colouring and the transferred colouring.If necessary, take a photo.If several passes are made, they should be performed with the same force and always in the same direction (i.e. after each pass, the tissue is lifted to be repositioned at the "start" of the strip so as to be reapplied on the deposit in the same way as in the previous pass). If necessary, take a photo between each step or only at the end of the evaluation. This type of process can be used to evaluate the overall resistance of the deposit.Water resistance:Insert the second made-up support, without folding it, into a centrifuge tube.Add 10 grams of demineralized water.Centrifuge for 10 minutes at 450×g.If necessary, take a photo of the support after mixing, immediately after the operation.Rub once with a tissue along the length of the support, without waiting, with the same force as that applied for the dry resistance.Observe the state of the rubbed support and the used surface of the tissue, in particular the remaining colouring and the transferred colouring.If necessary, take a photo.The protocol for multiple passes is the same as that detailed above for the dry resistance.Oil resistance:Perform the same protocol as for the water resistance, on the third made-up support, replacing the water with the same amount of olive oil (Refined Olive Oil - Aarhuskarlshamn).Grading:For each stress, record the result according to the table below:GradeState of the depositSurface of the material in contact with the deposit- -Total or partial removal of the deposit from the rubbed area; the surface of the support appears in placesVery intense colouring – very substantial to total colour transfer-Partial removal resulting in significantly and visibly less intense colouring of the deposit.Intense colouring – substantial colour transfer+Decrease in colour intensity of the deposit which is noticeable but does not reveal the supportMedium colouring – moderate colour transfer++No substantial change in the deposit colourSlight colouring – little colour transfer+++No variation in the deposit colourNo colouring or barely visible colouring – very little to no colour transferExample 1The following composition, the list of the ingredients and the contents of which are collated in the table below, was prepared:Ingredients – INCI nameComposition 1Dimethicone (Belsil DM 350; Wacker)5Lauroyl Lysine (Amihope LL; Ajinomoto)1.1Isododecane15Red 73.6Dimethicone (Xiameter PMX-200 Silicone Fluid 1000 CST; Dow)2.5Red 28 Lake9.2Nylon-611 / Dimethicone Copolymer (Dowsil 2-8179 Gellant; Dow)7.3Iron Oxide (and) Disodium Stearoyl Glutamate (and) Aluminium Hydroxide (NAI-C33-7001-10, Miyoshi)0.1C30-45 Alkyldimethylsilyl Polypropylsilsesquioxane (Dowsil SW-8005 C30 Resin Wax; Dow)2Silica Silylate (Dowsil VM-2270 Aerogel Fine Particles; Dow)0.7Dimethicone Crosspolymer (Dowsil EL-9240 Silicone Elastomer Blend, Dow, Dimethicone 2 cSt mixture)26.8Trimethylsiloxysilicate (Silsoft 74 Fluid, Momentive Performance Materials; in isododecane; 75% active material)17.6Dimethiconol (Dowsil PMX-1505 Fluid; Dow, in isododecane; 15% active material)8.4Preservatives / antioxidants0.7(Trimethylsiloxysilicate + Nylon-611 / Dimethicone Copolymer) / pigments weight ratio1.61. Preparation of the composition1- Prepare the ground pigmentary material by mixing the pigments in Dimethicone and a portion of the isododecane and then passing the mixture 3 times through a three-roll pigment mill.2- In a heating pan, introduce the Trimethylsiloxysilicate, Dimethiconol, Nylon-611 / Dimethicone Copolymer, C30-45 Alkyldimethylsilyl Polypropylsilsesquioxane and Lauroyl Lysine, at 100°C with stirring at 500 rev / min for 30 minutes in a Rayneri blender.3- Once the mixture is homogeneous, cool to 30°C and add the ground pigmentary material previously obtained, with stirring. Once the mixture has been homogenized, add the Dimethicone Crosspolymer and the rest of the isododecane with stirring at 600 rev / min for 20 minutes.4- Add the Silica Silylate with stirring, until a homogeneous mixture is obtained, at 600 rev / min.5- Lastly, add the preservatives and antioxidants and maintain the stirring for 15 minutes.6- Package the mixture in a suitable closed container.2. Evaluation of the compositionA fluid, stable, homogeneous composition is obtained, with a viscosity, measured according to the above protocol, of 19.1 poises.The composition is easily applied in a fine deposit, with a homogeneous colouring as soon as from the first pass. The deposit remains in place and does not migrate.The evaluation of the tack according to the above protocol is 37.3 J.m-2.The deposit is comfortable and remains so over time.The composition does not transfer (grade +++).Example 2The following compositions, the list of the ingredients and the contents of which are collated in the table below, were prepared:Ingredients – INCI nameComparative composition AComposition 2 of the inventionDimethicone (Belsil DM 350; Wacker)5.65.6Lauroyl Lysine (Amihope LL; Ajinomoto)1.11.1Isododecaneqs 100%qs 100%Red 71010Dimethicone (Xiameter PMX-200 Silicone Fluid 1000 CST; Dow)1.91.9Nylon-611 / Dimethicone Copolymer (Dowsil 2-8179 Gellant; Dow)8.28.2C30-45 Alkyldimethylsilyl Polypropylsilsesquioxane (Dowsil SW-8005 C30 Resin Wax; Dow)22Silica Silylate (Dowsil VM-2270 Aerogel Fine Particles; Dow)0.70.7Dimethicone Crosspolymer (Dowsil EL-9240 Silicone Elastomer Blend, Dow, in a Dimethicone 2 cSt)26.826.8Trimethylsiloxysilicate (Silsoft 74 Fluid, Momentive Performance Materials; in isododecane; 75% active material)19.519.5Dimethiconol (Dowsil PMX-1505 Fluid; Dow, in isododecane; 15% active material)-8.4(Trimethylsiloxysilicate + Nylon-611 / Dimethicone Copolymer) / pigments weight ratio2.32.31. Preparation of the compositionThe process is performed as for Example 1.2. Evaluation of the compositionsComposition AComposition 2Viscosity21.2 poises31.6 poisesTack (J.m-2)47.953.6TransferDry + / Water + / Oil - -Dry ++ / Water ++ / Oil ++The compositions are easily applied in a fine deposit, with a homogeneous colouring as soon as from the first pass. The deposit remains in place and does not migrate.However, the composition according to the invention has a significantly improved staying power in the three types of tests, of dry resistance, water resistance and oil resistance, compared to comparative composition A.Comparative Example 3The following composition, the list of the ingredients and the contents of which are collated in the table below, was prepared:Ingredients – INCI nameComparative composition BDimethicone (Belsil DM 350; Wacker)5.6Lauroyl Lysine (Amihope LL; Ajinomoto)1.1Isododecaneqs 100%Red 710Dimethicone (Xiameter PMX-200 Silicone Fluid 1000 CST; Dow)1.9Nylon-611 / Dimethicone Copolymer (Dowsil 2-8179 Gellant; Dow)12.5C30-45 Alkyldimethylsilyl Polypropylsilsesquioxane (Dowsil SW-8005 C30 Resin Wax; Dow)2Silica Silylate (Dowsil VM-2270 Aerogel Fine Particles; Dow)0.7Dimethicone Crosspolymer (Dowsil EL-9240 Silicone Elastomer Blend, Dow, in Dimethicone 2 cSt)26.8Trimethylsiloxysilicate (Silsoft 74 Fluid, Momentive Performance Materials; in isododecane; 75% active material)30Dimethiconol (Dowsil PMX-1505 Fluid; Dow, in isododecane; 15% active material)8.4(Trimethylsiloxysilicate + Nylon-611 / Dimethicone Copolymer) / pigments weight ratio3.51. Preparation of the compositionThe process is performed as for Example 1.2. Evaluation of the compositionComposition BViscosity113.6 poisesTack in J.m-2322.8TransferDry +++ / Water +++ / Oil ++The composition is quite easily applied in a fine deposit, with a homogeneous colouring as soon as from the first pass.The deposit remains in place and does not migrate, but it is tacky after application and over time.Comparative Example 4The following composition, the list of the ingredients and the contents of which are collated in the table below, was prepared:Ingredients – INCI nameComparative composition CDimethicone (Belsil DM 350; Wacker)5.6Lauroyl Lysine (Amihope LL; Ajinomoto)1.1Isododecaneqs 100%Red 713Dimethicone (Xiameter PMX-200 Silicone Fluid 1000 CST; Dow)1.9Nylon-611 / Dimethicone Copolymer (Dowsil 2-8179 Gellant; Dow)3.6C30-45 Alkyldimethylsilyl Polypropylsilsesquioxane (Dowsil SW-8005 C30 Resin Wax; Dow)2Silica Silylate (Dowsil VM-2270 Aerogel Fine Particles; Dow)0.7Dimethicone Crosspolymer (Dowsil EL-9240 Silicone Elastomer Blend, Dow, in a Dimethicone 2 cSt)26.8Trimethylsiloxysilicate (Silsoft 74 Fluid, Momentive Performance Materials; in isododecane; 75% active material)8.5Dimethiconol (Dowsil PMX-1505 Fluid; Dow, in isododecane; 15% active material)8.4(Trimethylsiloxysilicate + Nylon-611 / Dimethicone Copolymer) / pigments weight ratio0.81. Preparation of the compositionThe process is performed as for Example 1.2. Evaluation of the compositionComposition BViscosity12.4 poisesTack in J.m-214.6TransferDry - / Water + / Oil - - -The composition is easily applied in a fine deposit, with a homogeneous colouring as soon as from the first pass. The non-tacky deposit remains in place and does not migrate.However, the resistance in terms of the dry, water and oil tests is degraded.

Claims

Liquid cosmetic composition for making up human keratin materials, in particular the skin and / or the lips, preferably the lips, comprising, in a physiologically acceptable medium:- at least 20% by weight, relative to the total weight of the composition, of at least one first linear or branched, preferably saturated, non-polar hydrocarbon oil having from 8 to 16 carbon atoms,- at least one second oil chosen from volatile or nonvolatile silicone oils,- at least one silicone elastomer carried in hydrocarbon or silicone oil which may or may not be identical to the first oil(s) or to the second oil(s),- at least one silicone resin,- at least one silicone polyamide,- at least one silicone gum,- at least 8%, preferably at least 10% by weight, relative to the total weight of the composition, of pigments,- optionally water at a content of less than 5% by weight, preferably less than 3% by weight, relative to the total weight of the composition,- the (silicone resin + silicone polyamide) / pigment(s) weight ratio being between 1 and 2.7, preferably between 1 and 2.5.Cosmetic composition according to Claim 1, characterized in that the first non-polar hydrocarbon oil is chosen from branched C8-C16alkanes such as preferably Isododecane, Isodecane, Isohexadecane, C8-9 Isoalkane, C11-13 Isoalkane, and mixtures thereof; from linear, preferably C8-C13, alkanes, and mixtures thereof, such as preferably n-Dodecane, n-Tetradecane, C9-12 Alkane, the Undecane-Tridecane mixture; and also mixtures thereof; and preferably the first non-polar hydrocarbon oil is at least isododecane.Composition according to one of the preceding claims, characterized in that the content of first non-polar volatile hydrocarbon oil(s) ranges from 20% to 45% by weight, preferably from 25% to 35% by weight, relative to the total weight of the composition.Composition according to any one of the preceding claims, characterized in that the second oil is chosen from linear or cyclic volatile silicone oils, such as in particular those having the following INCI names: Cyclopentasiloxane, Cyclotetrasiloxane, Cyclohexasiloxane, Caprylyl Methicone, Disiloxane, Trisiloxane, Dimethicone in particular with a viscosity of less than 5 cSt, mixtures thereof, preferably from linear volatile silicone oils; from nonvolatile phenyl or non-phenyl silicone oils, in particular those having the following INCI names: Dimethicone, Alkyl Dimethicones in which the alkyl group is a C2-C24 alkyl group, phenyl silicones chosen from Phenyl Trimethicone, Diphenylsiloxy Phenyl Trimethicone; Trimethyl Pentaphenyl Trisiloxane; Trimethylsiloxyphenyl Dimethicone; Diphenyl Dimethicone; Tetramethyl Tetraphenyl Trisiloxane; and also mixtures thereof; preferably from the volatile or nonvolatile Dimethicones, and mixtures thereof.Composition according to any one of the preceding claims, characterized in that the composition comprises, as second silicone oil(s), at least one volatile, preferably linear, silicone oil, and at least one nonvolatile, preferably non-phenyl, silicone oil.Composition according to any one of the preceding claims, characterized in that the content of second silicone oil(s) ranges from 25% to 35% by weight, preferably from 27% to 32% by weight, relative to the total weight of the composition.Composition according to any one of the preceding claims, characterized in that the content of second nonvolatile silicone oil(s) ranges from 8% to 15% by weight, preferably 10% to 13% by weight, relative to the total weight of the composition.Composition according to one of the preceding claims, characterized in that the silicone resin is chosen from alkylsiloxysilicate, arylsiloxysilicate, alkylarylsiloxysilicate and polysilsesquioxane resins, and also mixtures thereof; more particularly from the silicone resins having the following INCI names: trimethylsiloxysilicate, polymethylsilsesquioxane, polypropylsilsesquioxane, and also mixtures thereof; the composition preferably comprising at least one trimethylsiloxysilicate resin.Composition according to one of the preceding claims, characterized in that the silicone resin is present in a content ranging from 10% to 20% by weight, preferably in a content ranging from 12% to 18% by weight, relative to the total weight of the composition.Composition according to any one of the preceding claims, characterized in that the silicone elastomer is chosen from the compounds having the following INCI names: Dimethicone Crosspolymer; Vinyl Dimethicone / Lauryl Dimethicone Crosspolymer; Dimethicone / Vinyl Dimethicone Crosspolymer; Dimethicone / Vinyltrimethylsiloxysilicate Crosspolymer, and also mixtures thereof, and preferably Dimethicone Crosspolymer.Composition according to any one of the preceding claims, characterized in that the oil carrying the silicone elastomer is chosen from the Dimethicones, in particular having a viscosity ranging from 1 to 500 cSt at 25°C, and from isododecane, alone or as a mixture.Composition according to any one of the preceding claims, characterized in that the content of silicone elastomer, expressed as active material, ranges from 2% to 8% by weight, preferably from 2.5% to 6% by weight, relative to the total weight of the composition.Composition according to any one of the preceding claims, characterized in that the silicone polyamide comprises at least one unit corresponding to the general formula (I):1) in which: G’ represents C(O) when G represents -C(O)-NH-Y-NH-, and G’ represents –NH- when G represents –NH-C(O)-Y-C(O)-,2) R4, R5, R6and R7, which may be identical or different, represent a group chosen from:saturated or unsaturated, linear, branched or cyclic C1to C40hydrocarbon groups, which may contain in their chain one or more oxygen, sulfur and / or nitrogen atoms, and which may be partially or completely substituted by fluorine atoms,C6to C10aryl groups, optionally substituted by one or more C1to C4alkyl groups,polyorganosiloxane chains possibly containing one or more oxygen, sulfur and / or nitrogen atoms,3) the groups X, which may be identical or different, represent a linear or branched C1to C30alkylenediyl group, possibly containing in its chain one or more oxygen and / or nitrogen atoms,4) Y is a saturated or unsaturated, divalent C1to C50, linear or branched alkylene, arylene, cycloalkylene, alkylarylene or arylalkylene group, which may comprise one or more oxygen, sulfur and / or nitrogen atoms, and / or may bear as substituent one of the following atoms or groups of atoms: fluorine, hydroxyl, C3to C8cycloalkyl, C1to C40alkyl, C5to C10aryl, phenyl optionally substituted by 1 to 3 C1to C3alkyl, C1to C3hydroxyalkyl and C1to C6aminoalkyl groups, orY represents a group corresponding to the formula: R8T<; in which- T represents a linear or branched, saturated or unsaturated, trivalent or tetravalent C3to C24hydrocarbon group optionally substituted by a polyorganosiloxane chain, and possibly containing one or more atoms chosen from O, N and S, or T represents a trivalent atom chosen from N, P and Al, and- R8represents a linear or branched C1to C50alkyl group or a polyorganosiloxane chain, possibly comprising one or more ester, amide, urethane, thiocarbamate, urea, thiourea and / or sulfonamide groups, which may possibly be linked to another chain of the polymer,6) n is an integer ranging from 2 to 500, preferably from 2 to 200, and m is an integer ranging from 50 to 1000, preferably from 50 to 700 and better still from 50 to 200.Composition according to any one of the preceding claims, characterized in that the silicone polyamide is at least chosen from the polymers having the INCI name Nylon-611 / Dimethicone Copolymer.Composition according to any one of the preceding claims, characterized in that the content of silicone polyamide ranges from 5% to 12% by weight, preferably 6% to 10% by weight, relative to the total weight of the composition.Composition according to any one of the preceding claims, characterized in that the silicone gum has the following formula:in which:- R7, R8, R11 and R12 are identical or different, and each is chosen from alkyl radicals comprising from 1 to 6 carbon atoms,- R9 and R10 are identical or different, and each is chosen from an alkyl radical comprising from 1 to 6 carbon atoms, an aryl radical, a hydroxyl radical, a vinyl radical, preferably an alkyl radical comprising from 1 to 6 carbon atoms, a hydroxyl radical;- X is chosen from an alkyl radical comprising from 1 to 6 carbon atoms, a hydroxyl radical, a vinyl radical, preferably an alkyl radical comprising from 1 to 6 carbon atoms, a hydroxyl radical;- n and p are chosen so as to confer upon the silicone gum a molecular mass of greater than or equal to 400 000 g / mol, and in particular may each take values ranging from 0 to 5000, knowing that n and p are not simultaneously zero.Composition according to any one of the preceding claims, characterized in that the silicone gum is a polydimethylsiloxane gum optionally comprising at least one aryl radical, a dimethiconol gum, or mixtures thereof, and preferably a dimethiconol gum.Composition according to any one of the preceding claims, characterized in that the silicone gum is present in a content, expressed as active material, ranging from 0.7% to 5% by weight, preferably from 1% to 2.5% by weight, relative to the total weight of the composition.Composition according to any one of the preceding claims, characterized in that the composition comprises at least one colorant, in particular chosen from mineral pigments, organic pigments, and also mixtures thereof.Composition according to any one of the preceding claims, characterized in that the pigment content represents from 8% to 15% by weight, preferably from 10% to 14% by weight, relative to the total weight of the composition.Composition according to any one of the preceding claims, characterized in that the composition comprises at least one wax chosen from polar or non-polar hydrocarbon waxes, or from silicone waxes, and also mixtures thereof; more particularly, the composition comprises at least one silicone wax, preferably the wax C30-45Alkyldimethylsilyl Polypropylsilsesquioxane (INCI name).Composition according to the preceding claim, characterized in that the content of wax(es) ranges from 1% to 5% by weight, in particular from 1.5% to 3.5% by weight, relative to the total weight of the composition.Composition according to any one of the preceding claims, characterized in that the composition optionally comprises water, in a content of less than or equal to 2% by weight, more particularly less than or equal to 1% by weight, advantageously less than or equal to 0.5% by weight, relative to the total weight of the composition.Composition according to any one of the preceding claims, characterized in that it optionally comprises at least one lipophilic thickener chosen from silicas, preferably hydrophobically treated silicas; lipophilic clays, and also mixtures thereof, and preferably silicas, preferably hydrophobically treated silicas.Composition according to the preceding claim, characterized in that the content of lipophilic thickener represents from 0.2% to 3% by weight, preferably from 0.5% to 1.5% by weight, relative to the total weight of the composition.Composition according to any one of the preceding claims, characterized in that it optionally comprises- at least one mineral filler, more particularly chosen from silica, perlite, calcium magnesium carbonate, kaolin, talc, natural or synthetic mica, boron nitride, glass or ceramic, and also mixtures thereof; advantageously in a content representing from 0.5% to 4% by weight, preferably from 1% to 3% by weight, relative to the total weight of the composition, and / or- at least one organic filler, chosen more particularly from micronized waxes, metal soaps, polysaccharides, cellulose, N-acylamino acids, particles of acrylic (co)polymers, of acrylonitrile (co)polymer, of polyurethane, of polyamide, of polytetrafluoroethylene, of silicone polymer or mixtures thereof; preferably N-acylamino acids; advantageously in a content representing from 0.5% to 5% by weight, preferably from 1% to 3% by weight, relative to the total weight of the composition.Composition according to any one of the preceding claims, characterized in that it optionally comprises at least one additional polar nonvolatile hydrocarbon oil, more particularly chosen from C10-C26alcohols; ethers of formula ROR’ or carbonates of formula RO(CO)OR’, in which formulae the groups R and R’, which may be identical or different, represent a saturated or unsaturated, branched or unbranched hydrocarbon group comprising at most 16 carbon atoms, preferably a C3-C16group; nonvolatile hydrocarbon ester oils comprising one or more ester functions and comprising at least one linear or branched, saturated, unsaturated or aromatic hydrocarbon group, the total number of carbon atoms preferably being at least 12, and optionally one or more ether or hydroxyl functions; mixtures thereof; the content of additional polar nonvolatile hydrocarbon oil(s), if the composition comprises same, being more particularly less than 5% by weight, more particularly less than 2% by weight, and more particularly still between 0.5% and 1.5% by weight, relative to the total weight of the composition, and preferably the composition does not comprise same.Composition according to any one of the preceding claims, characterized in that it optionally comprises at least one non-polar nonvolatile hydrocarbon oil, different from the first oil(s) and chosen from linear or branched hydrocarbons of mineral, plant or synthetic origin, and more particularly liquid paraffin, squalane of plant origin, isoeicosane, mixtures of linear saturated hydrocarbons such as C18-21 Alkane, C21-28 Alkane, hydrogenated or non-hydrogenated polybutenes, hydrogenated or non-hydrogenated polyisobutenes, hydrogenated or non-hydrogenated polydecenes, mixtures thereof; the content of additional non-polar nonvolatile hydrocarbon oil(s), if the composition comprises same, is less than 5% by weight, preferably less than 2% by weight, and more particularly still between 0.5% and 1.5% by weight, relative to the total weight of the composition.Process for making up and / or caring for the skin and / or the lips, in particular the lips, in which the composition according to any one of the preceding claims is applied.

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