Composition based on chitosan and a natural resin

Abstract

Composition based on chitosan and a natural resin. The present invention relates to a cosmetic composition, in particular for makeup and / or skin and / or lip and / or eyelash and / or hair care, especially for skin, comprising, in a physiologically acceptable aqueous medium: a) at least 0.01% by weight relative to the total weight of a native chitosan composition having a molecular weight strictly greater than 3000 Daltons, this amount being strictly less than 15% by weight, and b) at least one natural resin. It also relates to a method for applying makeup and / or skin and / or hair care products, in which the composition according to the invention is applied to the skin and / or hair. Figure for the abstract: none

Description

Title of the invention: Composition based on chitosan and a natural resin

[0001] The present invention relates to a cosmetic composition, in particular for makeup and / or care of the skin and / or lips and / or eyelashes and / or hair, comprising, in a physiologically acceptable aqueous medium:

[0002] a) at least 0.01% by weight relative to the total weight of the composition of native chitosan having a molecular weight strictly greater than 3000 Daltons, this quantity being strictly less than 15% by weight, and

[0003] b) at least one natural resin.

[0004] The present invention also relates to a method for making up and / or caring for the skin and / or the appendages, in which the composition according to the invention is applied to the skin and / or the appendages.

[0005] There are many cosmetic compositions for which properties of holding the deposited film, after application to keratin materials, are desired. Examples include lipsticks, foundations, mascaras or nail polishes. In order to obtain such a result, it is possible to combine particular raw materials, in particular film-forming agents.

[0006] Furthermore, we often seek to obtain covering compositions.

[0007] The formulator is therefore looking for raw materials and / or systems making it possible to obtain easily formulatable compositions, preferably fluid, based on chitosan, the deposit of which has good optical properties, for example, coverage, mattness, good hold and the resistance of which, for example to dry mechanical wear or to water, is improved. There is also a need for such compositions to also have good sensoriality on application and / or comfort on application, as well as a good texture, i.e. in particular which have a controlled and acceptable viscosity.

[0008] Furthermore, the formulation of environmentally friendly cosmetic products, i.e. those whose design and development take environmental issues into account, is becoming a major concern to help meet global challenges.

[0009] It is therefore essential to propose more sustainable compositions and / or preparation processes and / or ingredients, thus making it possible to respond to these environmental challenges.

[0010] In this context, it is important to develop new cosmetic compositions with a better carbon footprint, in particular by promoting the use of renewable raw materials and / or with a good index of naturalness and / or of natural origin and more particularly of plant origin while reducing the use of compounds of petrochemical origin.

[0011] These problems can be solved by the use of cosmetic compositions described below, these compositions having good formulability, good cosmetic properties, in particular good resistance of the makeup properties, such as coverage or mattness, under dry rubbing, in water, oils and / or sebum, as well as good sensoriality and good texture. The present invention aims in particular to provide emulsions comprising chitosan and having good resistance to dry rubbing, in water and / or in oil.

[0012] After application, these compositions leave a covering and homogeneous film-forming deposit, which has good wear resistance. The colored films formed are adhesive and cohesive, and have improved resistance when dry and / or in the presence of a chemical aggressor such as water.

[0013] These compositions also include sustainable ingredients, thus making it possible to respond to environmental issues.

[0014] The present invention therefore relates to a cosmetic composition, in particular for makeup and / or care of the skin and / or lips, in particular the skin and / or eyelashes and / or hair, comprising, in a physiologically acceptable aqueous medium:

[0015] a) at least 0.01% by weight relative to the total weight of the composition of native chitosan having a molecular weight strictly greater than 3000 Daltons, this quantity being strictly less than 15% by weight, and

[0016] b) at least one natural resin.

[0017] It also relates to a process for making up and / or caring for the skin and / or the appendages, in which the composition according to the invention is applied to the skin and / or the appendages.

[0018] The composition is preferably in the form of an emulsion, preferably a direct emulsion (oil-in-water) or an inverse emulsion (water-in-oil).

[0019] According to one embodiment, the composition according to the invention is in the form of an oil-in-water emulsion, having in particular an oily phase / aqueous phase weight ratio of between 5:95 and 80:20, preferably between 8:92 and 65:35, preferably between 10:90 and 60:40, preferably between 12:88 and 50:50, preferably between 15:85 and 40:60.

[0020] According to one embodiment, the composition according to the invention is in the form of a water-in-oil emulsion, having in particular an oily phase / aqueous phase weight ratio between 90:10 and 20:80, preferably between 80:20 and 30:70, preferably between 70:30 and 40:60, preferably between 65:35 and 45:55.

[0021] The composition according to the invention can also be in the form of an aqueous dispersion or solution or an aqueous gel.

[0022] By “physiologically acceptable” is meant a medium compatible with keratin materials.

[0023] Preferably, the composition according to the invention comprises, relative to the total weight of the composition, 10% by weight or less, preferably 5% by weight or less, preferably from 0.1 to 10% by weight, of silicone.

[0024] By silicone is meant any silicone compound.

[0025] Preferably, the composition according to the invention is substantially free of silicone other than a film-forming or tackifying silicone polymer, preferably other than a silicone resin or a silicone acrylate copolymer, preferably other than an MQ resin or an acrylates / poly-trimethylsiloxy-methacrylate copolymer.

[0026] By "substantially free of silicone other than a film-forming or tackifying silicone polymer, preferably other than a silicone resin or a silicone acrylate copolymer, preferably other than an MQ resin or an acrylates / polytrimethylsiloxy-methacrylate copolymer", it is meant that the composition comprises less than 1% by weight relative to the total weight of the composition, preferably less than 0.5% by weight, preferably less than 0.3% by weight, preferentially less than 0.1% by weight of silicone other than a film-forming or tackifying silicone polymer, preferably a silicone resin or a silicone acrylate copolymer, preferably other than an MQ resin or an acrylates / polytrimethylsiloxy-methacrylate copolymer.Preferably, the composition is completely free of silicone other than a film-forming or tackifying silicone polymer, preferably a silicone resin or a silicone acrylate copolymer, preferably other than an MQ resin or an acrylates / polytrimethylsiloxy-methacrylate copolymer. By silicone other than a film-forming or tackifying silicone polymer, preferably a silicone resin or a silicone acrylate copolymer, preferably other than an MQ resin or an acrylates / polytrimethylsiloxy-methacrylate copolymer, is meant any silicone compound which is not a film-forming or tackifying silicone polymer, preferably which is not a silicone resin or a silicone acrylate copolymer, preferably which is not an MQ resin or an acrylates / polytrimethylsiloxy-methacrylate copolymer.

[0027] The term "resin" means a compound whose structure is three-dimensional. Thus, for the purposes of the present invention, a polydimethylsiloxane is not a silicone resin.

[0028] The nomenclature for silicone resins is known as "MDTQ", the resin being described in terms of the different siloxane monomeric units that it includes each of the letters "MDTQ" characterizing a type of unit.

[0029] The letter "M" represents the Monofunctional unit of formula RlR2R3SiOi / 2, the silicon atom being linked to a single oxygen atom in the polymer comprising this unit.

[0030] The letter "D" means a Difunctional unit R1 R2SiO2 / 2 in which the silicon atom is linked to two oxygen atoms.

[0031] The letter “T” represents a Trifunctional unit of formula RlSiO3 / 2.

[0032] In the units M, D, T defined above, Ri, namely RI, R2 and R3, identical or different, represent a hydrocarbon radical (in particular alkyl) having from 1 to 10 carbon atoms, a phenyl group, a phenylalkyl group or even a hydroxyl group.

[0033] Finally, the letter "Q" signifies a Tetrafunctional SiO4 / 2 unit in which the silicon atom is linked to four oxygen atoms themselves linked to the rest of the polymer.

[0034] Such resins are described for example in "Encyclopedia of Polymer Science and Engineering, vol. 15, John and 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 US 5,082,706, US 5,319,040, US 5,302,685 and US 4,935,484.

[0035] Silicone resins of MQ type are, for example, alkylsiloxysilicates of formula [(Rl)3SiOi / 2]x(SiO4 / 2)y (MQ units) in which x and y are integers ranging from 50 to 80, and such that the RI group represents a radical as defined above, and preferably is an alkyl group having from 1 to 8 carbon atoms, or a hydroxyl group, preferably a methyl group. In particular, trimethylsiloxysilicate or phenylalkylsiloxysilicate resins such as phenylpropyldimethylsiloxysilicate are distinguished.

[0036] Silicone polymers include siloxanes having an organo-functional group, such as polyalkylsiloxanes, where at least one alkyl radical is other than methyl, for example organopolysiloxanes having the INCI name Stearyl Dimethicone, Cetyl Dimethicone or C26-28 Alkyl Dimethicone, or, for example, polyarylsiloxanes and polyarylalkylsiloxanes, for example organopolysiloxanes having the INCI name Phenyl Trimethicone, Trimethylsiloxyphenyl Dimethicone or Dimethylphenyl Dimethicone, or, for example, organopolysiloxanes having an organo-functional radical such as an aminopropyl, aminopropyl-aminoethyl, aminopropyl-aminoisobutyl radical, for example organopolysiloxanes having the INCI name Amodi-methicone, or, for example, organopolysiloxanes having a polyethylene glycol or polyalkylene glycol radical, for example organopolysiloxanes having the INCI name PEG-12 Dimethicone, PEG / PPG-25,25-Dimethicone or Cetyl PEG / PPG-15 / 15 Butyl ether Dimethicone.

[0037] Silicone acrylate copolymers are polymers comprising a group siloxane and a hydrocarbon group. For example, suitable polymers include polymers comprising a hydrocarbon backbone such as, for example, a backbone selected from vinyl polymers, methacrylic polymers and / or acrylic polymers and at least one chain selected from pendant siloxane groups and polymers comprising a backbone of siloxane groups and at least one pendant hydrocarbon chain such as, for example, a pendant vinyl, methacrylic and / or acrylic group.

[0038] The silicone acrylate copolymer may be selected from polymers derived from non-polar silicone copolymers comprising repeating units of at least one polar (meth)acrylate unit and vinyl copolymers grafted with at least one non-polar silicone chain. Non-limiting examples of such copolymers are acrylates / dimethicone copolymers such as those commercially available from Shin-Etsu, e.g., products sold under the trademarks KP-545 (cyclopentasiloxane (and) acrylates / dimethicone copolymer), KP-543 (butyl acetate (and) acrylates / dimethicone copolymer), KP-549 (methyl trimethicone (and) acrylates / dimethicone copolymer), KP-550 (INCI name: isododecane (and) acrylate / dimethicone copolymer), KP-561 (acrylates / stearyl acrylate / dimethicone acrylates copolymer), KP-562 (acrylates / behenyl acrylate / dimethicone acrylates copolymer), and mixtures thereof.Additional examples include acrylate / dimethicone copolymers sold by Dow Corning under the trademarks FA 4001 CM SILICONE ACRYLATE (cyclopentasiloxane (and) acrylates / polytrimethylsiloxymethacrylate copolymer), FA 4002 ID SILICONE ACRYLATE (isododecane (and) acrylates / polytrimethylsiloxymethacrylate Copolymer), and FA 4004 ID SILICONE ACRYLATE (isododecane (and) acrylates / polytrimethylsiloxymethacrylate Copolymer), and mixtures thereof.

[0039] According to one embodiment, the composition according to the invention is substantially free of silicone. By "substantially free of silicone" is meant that the composition comprises less than 1% by weight relative to the total weight of the composition, preferably less than 0.5% by weight, preferably less than 0.3% by weight, preferentially less than 0.1% by weight of silicone. Preferably, the composition is completely free of silicone. According to this embodiment, silicone is meant to mean any silicone compound, including film-forming or tackifying silicone polymers.

[0040] Preferably, the composition according to the invention comprises less than 20% by weight relative to the total weight of the composition of pullulan, preferably less than 10% by weight, preferably less than 5% by weight. Chitosan

[0041] The composition according to the invention comprises at least 0.01% by weight relative to the total weight of the composition of at least one native chitosan having a molecular weight strictly greater than 3000 Daltons (3 kDa).

[0042] The quantity of native chitosan is also strictly less than 15% by weight relative to the total weight of the composition.

[0043] Preferably, the native chitosan has a molecular weight greater than or equal to 10 kDa, preferably greater than or equal to 15 kDa, preferably greater than or equal to 20 kDa. Preferably, the native chitosan has a molecular weight of between 10 kDa and 2 MDa, preferably between 15 kDa and 1.5 MDa, preferably between 20 kDa and 300 kDa, preferably between 20 kDa and 200 kDa. One Dalton is equivalent to 1 g / mol.

[0044] Chitosan (or chitosan) is very rare in nature. It is only reported in the exoskeletons of certain insects such as termite queens and in the cell walls of a particular class of fungi, the zygomycetes.

[0045] Chitosan is obtained by deacetylation of chitin. Chitin is a polysaccharide composed of several N-acetyl-D-glucosamine units linked together by a [3 (1,4)] type bond.

[0046] The ideal chemical structure of chitosan is a chain of monomers [3-D-glucosamine linked by a glycosidic bond (1—>4).

[0047] By "chitosan" according to the invention is meant any copolymer formed from constituent units N-acetyl-D-glucosamine and D-glucosamine, the degree of acetylation of which is less than 90%. Chitosan is made up of glucosamine sugar units (deacetylated units) and N-acetyl-D-glucosamine units (acetylated units) linked together by bonds of type [3 (1,4) and constitutes a polymer of the type Poly(N-acetyl-D-glucosamine) -poly(D-glucosamine).

[0048] Preferably, the degree of acetylation of the chitosan is less than or equal to 80%, preferably less than or equal to 70%, preferably less than or equal to 60%, preferably less than or equal to 50%, preferably less than or equal to 35%, preferably less than or equal to 25%, preferably less than or equal to 15%.

[0049] The degree of acetylation is the percentage of acetylated units relative to the number of total units, it can be determined by Fourier transform infrared spectroscopy (FT-IR) or by titration with a strong base.

[0050] The chitosan of the invention is preferably a polysaccharide prepared from a fungal origin. It is in particular extracted and purified from safe and abundant food or biotechnological fungal sources such as Agaricus bisporus or As-pergillus niger.

[0051] The chitosan of the invention is preferably derived from the mycelium of a fungus of the Ascomycete type, and in particular Aspergillus niger and / or a Basi-diomycete fungus, and in particular Le ntinula edodes (shiitake) and / or Agaricus bisporus. preferably the fungus is Aspergillus niger.

[0052] The chitosan may be of GMO origin, but preferably is of non-GMO origin.

[0053] The chitosan according to the invention is native, that is to say that it is not modified. In particular, it does not contain any chemical modification.

[0054] A method for preparing chitosan is that described in application WO03068824.

[0055] Preferably, the chitosan used in the invention is in powder form. It is notably marketed by Kitozyme under the name Kiosmetine or Kionutrime.

[0056] The chitosan is preferably present in an amount ranging from 0.01% to 14% by weight, preferably from 0.1% to 14% by weight, preferably from 0.1% to 12% by weight, preferably from 0.2% to 7% by weight, preferably from 0.25% to 5%, preferably from 0.3 to 3% by weight, or even more preferably from 0.5 to 2% by weight relative to the total weight of the composition. Natural resin

[0057] The composition according to the invention comprises at least one natural resin.

[0058] A resin is generally defined as a solid, highly viscous or liquid substance, of plant or synthetic origin. Resins have several specific characteristics, such as:

[0059] - the ability to harden permanently, for example for synthetics under the influence of temperature and for natural ones under the influence of oxygen;

[0060] - their insolubility in water and especially their good sticky and adhesive properties.

[0061] The ISO4618:2014(fr) standard defines a resin as being a “generally amorphous macromolecular product, with a consistency ranging from solid to liquid state”.

[0062] Natural resins are almost exclusively of plant origin (fossil or harvested), and are secreted and then exuded from plants for defense, protection and communication roles within their ecosystem. Shellack of animal origin, secreted by the insect Coccus lacca, is an exception.

[0063] By "natural resin", and in particular "plant resin", within the meaning of the invention, is meant any substance comprising a minimum content of terpene compounds, that is to say at least 30% by weight of terpene compounds on the total weight of the substance (or material) considered, as chemically defined below, said substance being derived directly or indirectly, from the secretion and exudation, mainly by plants (more rarely by animals), of a substance for roles of defense, protection and communication with their ecosystem.

[0064] Advantageously, the natural resin according to the invention is not soluble in water at room temperature (unlike latex or gums for example).

[0065] Natural resins are also considered as natural glues which have the inherent ability to polymerize consistently and predictably on their own without synthetic chemistry.

[0066] Preferably, the natural resin used in the composition according to the invention has a number-average molecular weight of less than or equal to 10,000 g / mol. The resin preferably has a number-average molecular weight of less than or equal to 10,000 g / mol, in particular ranging from 250 to 10,000 g / mol, preferably less than or equal to 5,000 g / mol, in particular ranging from 250 to 5,000 g / mol, better still, less than or equal to 2,000 g / mol, in particular ranging from 250 to 2,000 g / mol, and even better still less than or equal to 1,000 g / mol, in particular ranging from 250 to 1,000 g / mol. The number-average molecular weights (Mn) are determined by gel permeation liquid chromatography (THF solvent, calibration curve established with linear polystyrene standards, refractometric detector). Thermal properties

[0067] Advantageously, the resins according to the invention are characterized by the fact that they have a softening point, which designates the transition temperature from a pseudo-solid state to a plastic state upon heating.

[0068] Preferably, the resins of the invention have a softening point (or temperature) in the range of 20°C to 150°C, more preferably 30°C to 100°C, even more preferably 40°C to 90°C.

[0069] The softening point is the temperature at which a product reaches a certain degree of softening under standard conditions. It designates the transition temperature from a pseudo-solid state to a plastic state upon heating. It can be measured by the ring and ball method (or TBA, ring and ball temperature) for resins according to ASTM E284.

[0070] Depending on their class, some of the resins according to the invention may also have a melting temperature, preferably less than 360°C, preferentially less than 190°C, and even more preferentially less than 90°C.

[0071] According to a preferred form of the invention, the resins do not have a melting temperature.

[0072] The melting point (or melting temperature) of a substance at a given pressure corresponds to the temperature at which the liquid and solid states of this substance can coexist in equilibrium.

[0073] Preferably, the resins of the invention have a glass transition temperature, this being preferably in the range from 0 to 200°C, more preferably from 10°C to 100°C, even more preferably from 20°C to 90°C and even more preferably from 30°C to 70°C.

[0074] The glass transition temperature (Tg) of a material represents the temperature range through which the material passes from one state rubbery to a glassy, ​​solid (rigid) state.

[0075] The thermal properties, in particular the Tf and Tg of the resins, can be measured by DSC (Differential Scanning Calorimetry), for example using a Perkin Elmer DSC 8000 device, according to:

[0076] - Protocol 1: Determination of melting temperatures Tf and crystallization Te: The raw materials alone or solubilized / dispersed in solvents, stainless steel cups, sweeping from 5°C to 90°C, sweeping speed at 5°C.min-l;

[0077] - Protocol 2: Determination of the glass transition temperature Tg: measurement in 2nd heating. Aluminum cups (40 qL) are used containing the raw materials, a temperature scan between -100°C and 150°C (with isotherms) is carried out in order to observe the glass transition temperature. The temperature ramp applied is 10°C / min for the glass transition temperatures (2 cycles).

[0078] Chemically, natural resins are complex mixtures of several classes of compounds whose presence and content define the class of resin (oleoresin, balsam, gum, etc.): essential oils, neutral and acid constituents and polysaccharides (present exclusively in gums).

[0079] The characteristic components of the resins are the terpene compounds which they contain, preferably in a content of at least 30% by weight, based on the weight of resin.

[0080] By "terpene compounds" we mean terpenes, hydrocarbons formed from isoprene of general formula (C5H8)n, and their numerous derivatives (alcohols, aldehydes, ketones, acids, etc.) comprising a terpene structure (Academy of Montpellier. Resins: https: / / tice.ac-montpellier.fr / ABCDORGA / Famille / Terpenes.html).

[0081] Among the terpene hydrocarbons, we distinguish: monoterpenes of empirical formula C10H16 (n=2), sesquiterpenes of empirical formula C15H24 (n=3), diterpenes (C20H32) (n=4), sesterterpenes (C25H40) (n=5), triterpenes (C30H48) (n=6), tetraterpenes (C40H64) (n=8) and other polyterpenes. Some have an acyclic structure; they have a number of double bonds corresponding to their empirical formula: 3 for C10H16; 5 for C20H32; 7 for C30H48. Others have one or more cycles, i.e. a smaller number of double bonds; for example for C10H16 one cycle and 2 double bonds or 2 cycles and one double bond.

[0082] Advantageously, the resins of the invention contain at least 30% of terpene compounds, preferably at least 40% by weight of terpene compounds, preferably at least 50% of terpene compounds, and even more preferably at least 60% of terpene compounds, or even better at least 70%, by weight of the total weight of resin or resinous substance used as raw material in the composition according to the invention.

[0083] Monoterpene and sesquiterpene compounds are mostly volatile compounds, constituting for example essential oils. Polyterpene compounds derived from terpenes with n greater than or equal to 4 (such as derivatives of diterpenes and triterpenes) are resinous compounds of a rather solid nature.

[0084] According to a preferred embodiment of the invention, the resins comprise at least 10%, preferably at least 20% by weight, preferably at least 30% by weight, preferably at least 35% by weight, of polyterpene compounds, i.e. derived from terpenes with n greater than or equal to 4, out of the total weight of the resin representing 100%. Thus, resins having a solid fraction at room temperature (25°C) are preferred. Advantageously, said resins used according to the invention are not volatile.

[0085] Advantageously, the polyterpene compounds of the resins or resinous substances used in the composition of the invention are predominantly (more than 50% by weight of the total weight of polyterpenes) derived from diterpenes and / or triterpenes.

[0086] According to a preferred embodiment of the invention, the resins comprise less than 70% by weight of monoterpene or sesquiterpene compounds, i.e. derived from terpenes with n less than 4, on the total weight of the resin representing 100%, preferably said resins comprise less than 60% by weight, preferably less than 50% by weight, preferably less than 30% by weight, preferably less than 15% by weight, of monoterpene or sesquiterpene compounds, derived from terpenes with n less than 4, on the total weight of the resin representing 100%. It is thus preferred, for the compositions of the invention, to limit the use of the most volatile resins, because they are less effective in terms of cosmetic film strength.

[0087] Advantageously, the natural resin(s) according to the invention are chosen from: a) acaroid resins, b) ambers, c) asphaltite and gilsonite, d) Peruvian balsam, e) Tolu balsam, f) Benzoin resins, g) Canada balsam, h) copal resins (in particular Kauri copal resins, Manila copal resins, West African copals such as Congo, Angola or Cameroon copals, East African copals such as Zanzibar or Madagascar copals, South American copals such as Brazilian or Colombian copals), i) damars, j) elemis, k) incenses, 1) Galbanums, m) labdanums, n) mastics or mastics, o) Myrrh, p) Sandarac, q) Shellacs, r) Styrax (Storax), s) Venetian Turpentine (Larch, Turpentine), t) Colophony, including Rosin and Rosinate and Tall Oils, v) Resins extracted from vegetable waxes; and mixtures of these resins.

[0088] Preferably, the natural resin(s) used according to the invention are chosen from j), k), t) and v); it is understood that the resin(s) of the invention may be esterified, salified, form adducts, be modified by phenols, and / or dimerized and / or further hydrogenated.

[0089] j) The elemis

[0090] "Ëlemis" is the generic term to define the group of recent natural resins Derived from plants of the Burseraceae (Canarium indicum) family. Each type is described according to its country of origin. According to a particular embodiment of the invention, the elemi resin used comes from the Philippines, particularly Manila elemi. To extract it, the trees are injured and a pathological resin discharge appears, which solidifies over time. Elemi are yellowish to greenish in color, opaque, ointment-like, sticky, and solidify into brownish resins dotted with crystals.

[0091] Elemis are soluble in aromatic solvents, alcohols, esters and carbon disulfide; and less soluble in aliphatic solvents. Elemis have an acid number between 18 and 34, a saponification value between 25 and 60, and a softening point of approx. 80. Balms exuding from elemis contain up to 30% essential oils.

[0092] According to a preferred embodiment of the invention, the resin(s) of the invention are chosen from elemi, in particular elemi from the Canarium Luzonicum family in its pure form or mixed with a latex, for example. Mention may be made of the elemi resin from Canarium Luzonicum marketed under the name ELEMI RESIN.

[0093] k) Incense

[0094] Incenses are present in the United Arab Emirates, Oman, Somalia, Ethiopia and eastern India. Frankincense resins are recent and derived from the Boswellia carterii tree incense. Amazonian frankincense resins are also found. The bark is intentionally wounded to obtain a milky extract which is recovered after drying. Preferably, the resin(s) of the invention are chosen from incense, in particular from the Amazon.

[0095] Frankincense resins are pale yellow, form irregular rounded or globular beads. They generally contain 20% to 40% by weight (approx. 33%) of boswellic acid (C32H52O4). Incenses have an acid number between 30% and 50% (indirect) and are moderately soluble in ethanol in alkaline media.

[0096] According to a particular embodiment of the invention, the resin(s) of the invention are chosen from incense, in particular Amazonian incense resins marketed under the name Protium heptaphyllum resin, or PROTIUM RESIN, or WHITE BREU RESIN, and incense resins from the Sal tree, Shorea robusta.

[0097] Advantageously, the resin(s) are in a mixture with one or more fatty substances as defined below according to the invention, preferably chosen from volatile or non-volatile oils. Examples that may be mentioned are Shorea robusta resin with sunflower seed oil (SHOREA ROBUSTA RESIN, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, TOCOPHEROL: 50-75% by weight shorea robusta resin, 25-50% by weight sunflower seed oil) marketed under the name KAHLRESIN 6720, and Shorea robusta resin with octyldodecanol (SHOREA ROBUSTA RESIN and OCTYLDODECANOL 50-70% by weight shorea robusta resin, 30-50% by weight octyldodecanol) marketed by KAHLRESIN 6720.

[0098] t) Rosins

[0099] Preferably the natural resin(s) are chosen from rosins. Rosins are recent resins, from renewable resources, and can be modified (e.g. esterified, hydrogenated, substituted).

[0100] Rosin gums are preferably purified, distilled, from the balsam of various pine essences (up to 80 different species).

[0101] Their composition is determined by climate, soil composition, and other botanical and meteorological factors. For example, we can cite rosins from Pinus austriaca (black pine) Austria, Central America, caribaea (slash pine), United States, Caribbean, densiflora Japan, elliottii United States, halepensis (Aleppo pine) Greece, Portugal, Spain, langifolia India, maritima (seashore pine) France, Spain, Portugal, massoniana (Chinese red pine) China, mercusii Indonesia, Burma, Philippines, nigra (black pine) Austria, oocarpa Central America, Honduras, palustris (swamp pine), United States, (longleaf pine), pseudostrobus Central America, Mexico, sylvestris (Scots pine) Germany, Poland, tonkinensis China, yunnanensis China.

[0102] The average composition is approx. 70 to 75% rosin and 20 to 25% turpentine.

[0103] Wood rosin [8050-09-7]

[0104] Rosin comes from stumps in the USA that have remained in the ground for at least 10 years so that the resin-rich heartwood is available.

[0105] The pine stumps contain between 10 and 30% by weight (approx. 19% rosin), between 1 and 10% by weight (preferably 4%) of turpentine oil, between 1 and 10% by weight (preferably 4%) of resins insoluble in petroleum ether, between 20 and 30% by weight (preferably 23%) of water and between 40 and 60% by weight (preferably 50%) of cellulose and lignin type.

[0106] According to a particular embodiment of the invention, the resin(s) are chosen from rosins.

[0107] Tall oils rosin (Rosin and rosinate) [8052-10-6]

[0108] Rosin tall oils often contain small amounts of higher fatty acids, particularly with a carbon atom number greater than or equal to 6 carbon atoms. According to one embodiment, the rosin tall oils are free of oxocarboxylic acid. In particular, they are soluble in organic solvents.

[0109] The rosin resins of the invention comprise in particular rosin acids belonging to the terpenes. The numbering of the carbon atoms in the rosin acid molecules is indicated using abietic acid as an example.

[0110] Rosin acids have the molecular chemical formula C2o H30 O2 and therefore belong to the diterpene family (four isoprene units). A large number of isomers exist of tricyclic rosin acids which differ in the position of the two double bonds.

[0111] Advantageously, said resin according to the invention is chosen from: gum rosin obtained by incision on living trees, wood rosin which is extracted from stumps or pine wood, and tall oil rosin which is obtained from a by-product from paper production. Advantageously, said resin(s) comprise rosin acids; preferably mainly chosen from abietic and pimaric type acids; and in particular chosen from: levopimaric acid, neoabietic, abietic, dehydroabietic, tetrahydroabietic, dihydroabietic, dextropimaric, isodextropimaric acid; or palustric acid; and mixtures thereof.

[0112] The rosin derivatives may be derived in particular from the polymerization, hydrogenation and / or esterification (for example with polyhydric alcohols such as ethylene glycol, glycerol, pentaerythritol) of rosin acids. Examples that may be mentioned are the rosin esters marketed under the reference FORAL 85, PENTALYN H and STAYBELITE ESTER 10 by the company HERCULES; SYLVATAC 95 and ZONESTER 85 by the company ARIZONA CHEMICAL or UNIREZ 3013 by the company UNION CAMP.

[0113] According to one embodiment of the invention, the resin(s) are chosen from rosinates (salts of alkaline agents of rosin acids, in particular salts of alkali metals such as sodium or potassium, alkaline earth metals such as calcium, or metals such as zinc or magnesium).

[0114] According to another preferred embodiment of the invention, the resin(s) are chosen from rosin acid esters, in particular rosin acid esters as defined above and (C1-C6) alkanol, polyhydroxy(Cl-C6)alkane polyols such as glycerol, pentaerythritol, and mixtures thereof, more preferably chosen from glyceryl rosinate sold under the name RESIESTER GUM A 35, glyceryl rosinate mixed with a vegetable oil hy drugged and / or castor seed oil (GLYCERYL ROSINATE, RICINUS COMMUNIS SEED OIL, HYDROGENATED VEGETABLE OIL marketed under the name EFP BIOTEK) pentaerythrityl rosinate marketed under the name RESIESTER N 35 S and RESIESTER 80.

[0115] According to another embodiment of the invention, the resin(s) are chosen from poly(carboxy)(C2-C6) alkane or poly(carboxy)(C2-C6) alkene adducts, in particular of maleic acids with rosin acids.

[0116] According to another embodiment of the invention, the resin(s) are chosen from rosins modified by phenols. In particular those modified by (C1-C4) alkylene phenols or diphenols, optionally substituted by one or more (C1-C4) alkyl groups such as methyl or t-butyl, more particularly rosins modified by 4-tert-butylphenol and 4,4'-isopropylidenediphenol (bisphenol A).

[0117] According to another embodiment of the invention, the resin(s) are chosen from dimerized rosins; in particular those in which the abietic acid is polymerized. Preferably, the rosins contain more than 50% of dimer acids and are thus called dimerized rosins. According to one embodiment, the rosins are polymerized and contain from 30% to 90% by weight of dimer acid (in particular at least 40%, 60 or 80% of dimer acids).

[0118] According to a preferred embodiment of the invention, the resin(s) are chosen from hydrogenated rosins. The double bonds, in particular acids such as abietic acid, are subject to oxidation, which can be eliminated by hydrogenation. It is understood that the resin(s) of the invention can be esterified, salified, adducted, modified by phenols, and / or dimerized and further hydrogenated.

[0119] According to a preferred embodiment, the resin comprises at least one rosin acid ester selected from the group consisting of glyceryl rosinate, pentaerythrityl rosinate, silicone rosinate, diethylene glycol rosinate, hydrogenated dilinoleyl dimer rosinate, dipentaerythrityl hexahydroxystearate / hexastearate / hexarosinate, glyceryl dibehenate / hydrogenated rosinate, glyceryl diisostearate / hydrogenated rosinate, trihydrogenated glyceryl rosinate, glycol rosinate, hydrogenated methyl rosinate, methyl rosinate, hydrogenated pentaerythrityl rosinate, hydrogenated triethylene glycol rosinate; and mixtures thereof.

[0120] According to a particular embodiment, the resin(s) of the invention are chosen from hydrogenated pentaerythrityl rosinate (PENTAERYTHRITYL HYDROGENATED ROSINATE), hydrogenated methyl rosinate (METHYL HYDROGENATED ROSINATE) marketed under the name SYMRISE BIO4326.

[0121] In addition, the resin(s) of the invention may be mixed with fatty substances, in particular waxes or butters. Mention may be made of mixtures of glyceryl rosinate with one or more fatty substances, in particular chosen from waxes or butters. butters such as blending with shea butter or olive oil such as (GLYCERYL ROSINATE, RICINUS COMMUNIS SEED OIL, HYDROGENATED VEGETABLE OIL), BUTYROSPERMUM PARKII (SHEA BUTTER) GLYCERYL ROSINATE, OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES GLYCERYL ROSINATE, OLEA EUROPAEA(OLIVE) OIL UNSAPONIFIABLES marketed by SHEA BUTTER & GLYCERYL ROSINATE & OILS.

[0122] v) resins extracted from vegetable waxes

[0123] Natural plant waxes as such are not considered resins. Although they are among the substances secreted / excreted by plants and naturally contain a very low resin content, they contain less than 30% by weight of terpenes on the total weight of wax. For example, Camauba wax is naturally secreted by the leaves of a Copernica Cerifera palm to prevent the leaves from dehydrating. Candelilla wax is obtained from a shrub called Euphorbia Antisyphilitica native to Northern Mexico. The wax protects the plant from its environment and prevents excessive evaporation. For example, candelilla wax consists primarily of hydrocarbons (about 50%, chains of 29 to 33 carbon atoms), higher molecular weight esters (20 to 29%), free acids (7 to 9%), and resins (12-14%, primarily triterpene esters).

[0124] Nevertheless, the definition of "natural resins" within the meaning of the present invention also includes resins derived from vegetable waxes, when they have been previously concentrated, isolated or extracted from these waxes, provided that the resinous or terpenic ingredient considered contains the minimum terpene content (30% by weight of the total weight of the ingredient) required by the present invention. Mention may in particular be made of Candelilla resin (100% pure resin extracted from the corresponding wax), with the INCI name: EUPHORBIA CERIFERA (CANDELLILA) WAX EXTRACT, marketed under the name CANDELILLA RESIN El by JAPAN NATURAL PRODUCTS.Document WO2013 / 147113 A1 also refers to Camauba resin, a terpene resin extracted from Camauba wax, and having physical properties similar to those of the natural resins classically described, such as a softening temperature and not a melting temperature which differentiates the resin from the wax.

[0125] Table 1 of the examples shows certain characteristic differences between the waxes and resins according to the invention, concerning their thermal properties.

[0126] The resins have a softening point and a glass transition temperature, but no melting temperature.

[0127] The opposite is true for waxes that have a melting temperature.

[0128] Preferably, the resin(s) are chosen from the resin(s) j), k), and t) as defined above, and the resins v) extracted from waxes, in particular from candelilla, or camauba; and mixtures thereof.

[0129] According to a preferred embodiment of the invention, the resin(s) are chosen from the following references, indicated by their INCI name, used alone or as a mixture:

[0130] - resins extracted from vegetable waxes (type v resins), preferably extracts EUPHORBIA CERIFERA (CANDELILLA) wax, such as CANDELILLA RESIN El marketed by JAPAN NATURAL PRODUCTS, BOTANICAL RESIN marketed by CERA RICA NODA, TOWAX-1F12 marketed by TOA KASEI;

[0131] - incense resins (type k resins), preferably PROTIUM HEP- TAPHYLLUM RESIN, or PROTIUM RESIN, or WHITE BREU RESIN, which can be marketed for example by CITROLEO or Ephyla;

[0132] - incense resins from the Sal tree, SHOREA ROBUSTA RESIN. The resins may be found in a mixture with one or more fatty substances, preferably chosen from volatile or non-volatile oils. Examples include Shorea robusta resin with sunflower seed oil (SHOREA ROBUSTA RESIN, HE-LIANTHUS ANNUUS (SUNFLOWER) SEED OIL, TOCOPHEROL: 50-75% by weight shorea robusta resin, 25-50% by weight sunflower seed oil) marketed under the name KAHLRESIN 6720, and Shorea robusta resin with octyldodecanol (SHOREA ROBUSTA RESIN and OCTYLDODECANOL 50-70% by weight shorea robusta resin, 30-50% by weight octyldodecanol) marketed by KAHLRESIN 6720 (type k resin); and

[0133] - rosins (t-type resins), preferably rosin acid esters (rosin) such as GLYCERYL ROSINATE marketed under the name RESIESTER GUM A 35, glyceryl rosinate mixed with hydrogenated vegetable oil and / or castor seed oil (GLYCERYL ROSINATE, RICINUS COMMUNIS SEED OIL, HYDROGENATED VEGETABLE OIL marketed under the name EFP BIOTEK), pentaerythrityl rosinate marketed under the name RESIESTER N 35 S and RESIESTER 80 or hydrogenated rosinates such as hydrogenated pentaerythrityl rosinate (PENTAERYTHRITYL HYDROGENATED ROSINATE) or hydrogenated methyl rosinate (METHYL HYDROGENATED ROSINATE) marketed under the name SYMRISE BIO4326.

[0134] According to a preferred embodiment of the invention, the resin(s) are chosen from resins extracted from EUPHORBIA CERIFERA (CANDELILLA) wax, incense resins such as PROTIUM HEPTAPHYLLUM RESIN, or PROTIUM RESIN, or WHITE BREU RESIN, incense resins from the Sal tree such as SHOREA ROBUSTA resin and GLYCERYL ROSINATE. According to a preferred embodiment of the invention, the resin(s) are chosen from resins extracted EUPHORBIA CERIFERA (CANDELILLA) wax, incense resins such as PROTIUM HEPTAPHYLLUM RESIN, or PROTIUM RESIN, or WHITE BREU RESIN and incense resins from the Sal tree such as SHOREA ROBUSTA resin.

[0135] According to a preferred embodiment of the invention, the resin(s) are chosen from EUPHORBIA CERIFERA (CANDELLILA) WAX EXTRACT.

[0136] Advantageously, the resin(s) is(are) present in the composition of the invention in a content within the range of 0.1% to 40%, preferably 0.2% to 30%, preferably 0.8% to 22%, preferably 1 to 20%, and more preferably 1.2% to 15%, preferably 1.5% to 10%, or even more preferably 2% to 8% by weight relative to the total weight of the composition.

[0137] Advantageously, the composition of the present invention comprises less than 10%, preferably less than 5%, preferably less than 1%, preferably less than 0.5%, preferably less than 0.1%, preferably is free, of synthetic resin.

[0138] Advantageously, the composition of the present invention comprises less than 10%, preferably less than 5%, preferably less than 1%, preferably less than 0.5%, preferably less than 0.1%, preferably is free of silicone resin, i.e. synthetic resin in which the basic structure is a chain comprising siloxane groups (silicon-oxygen-silicon bonds).

[0139] According to one embodiment, the composition according to the invention comprises a weight ratio between the chitosan and the natural resin (i.e. chitosan:natural resin weight ratio) of between 0.00025 and 150, preferably it is between 0.001 and 100. Preferably, it is between 0.01 and 50, preferably between 0.05 and 10, and even more preferably between 0.1 and 2.5. Pigmentary coloring matters

[0140] The composition according to the invention may further comprise at least one pigmentary coloring matter. This coloring matter is chosen from powdery coloring matters such as mineral pigments, pearlescent agents, organic pigments.

[0141] The term “pigments” means white or colored particles, mineral or organic, insoluble in an aqueous medium, intended to color the composition and / or the resulting deposit.

[0142] The coloring materials may be present in the composition in a content ranging from 0.5% to 70% by weight, preferably from 1% to 60% by weight, preferably from 1% to 50% by weight, preferably from 2% to 40% by weight, relative to the weight of the composition, preferably from 4% to 30% by weight, preferably from 5% to 25% by weight, preferably from 6% to 20% by weight, preferably from 8% to 18% by weight. Mineral pigments

[0143] According to a particular embodiment, the pigments used according to the invention are chosen from mineral pigments.

[0144] By "mineral pigment" is meant any pigment that meets the definition of the Ullmann encyclopedia in the inorganic pigment chapter. Among the mineral pigments useful in the present invention, mention may be made of zirconium or cerium oxides, as well as zinc, iron (black, yellow or red) or chromium oxides, manganese violet, ultramarine blue, chromium hydrate and ferric blue, titanium dioxide, metal powders such as aluminum powder and copper powder. The following mineral pigments may also be used: Ta2O5, Ti3O5, Ti2O3, TiO, ZrO2 in mixture with TiO2, ZrO2, Nb2O5, CeO2, ZnS.

[0145] The size of the pigment useful in the context of the present invention is generally greater than 5 nm, preferably greater than 10 nm, preferably greater than 20 nm, preferably greater than 100 nm and can range up to 10 qm, preferably from 200 nm to 5 qm, and more preferably from 300 nm to 1 qm. According to a particular form of the invention, the pigments have a size characterized by a D

[50] greater than 100 nm and which can range up to 10 qm, preferably from 200 nm to 5 qm, and more preferably from 300 nm to 1 qm. The sizes are measured by static light scattering using a commercial granulometer such as the Malvern MasterSizer 3000®, which allows the size distribution of all particles to be measured over a wide range from 0.01 qm to 1000 qm. The data are processed based on classical Mie scattering theory.This theory is most suitable for size distributions ranging from submicron to multi-micron, it allows to determine an "effective" particle diameter. This theory is notably described in the work of Van de Hulst, HC, "Light Scattering by Small Particles", Chapters 9 and 10, Wiley, New York, 1957. D

[50] represents the maximum size that 50% by volume of the particles presents.

[0146] In the context of the present invention, the mineral pigments are more particularly iron oxide and / or titanium dioxide. By way of example, mention may be made more particularly of titanium dioxides and iron oxides, coated with aluminum stearoyl glutamate, for example marketed under the reference NAI® by the company MIYOSHI KASEI.

[0147] As mineral pigments which can be used in the invention, mention may also be made of nacres.

[0148] By “mother-of-pearl” we mean colored particles of any shape, iridescent or not, in particular, produced by certain molluscs in their shell or synthesized and which present a color effect by optical interference.

[0149] The nacres can be chosen from pearlescent pigments, such as titanium mica coated with iron oxide, titanium mica coated with iron oxychloride, or titanium mica coated with iron oxychloride. bismuth, titanium mica coated with chromium oxide, titanium mica coated with an organic colorant, as well as pearlescent pigments based on bismuth oxychloride. They may also be mica particles on the surface of which are superimposed at least two successive layers of metal oxides and / or organic colorants. Examples of pearlescent pigments include natural mica coated with titanium oxide, iron oxide, natural pigment or bismuth oxychloride. Among the mother-of-pearls available on the market, we can cite the TIMICA®, FLAMENCO® and DUOCHROME® mother-of-pearls (mica-based) marketed by the company ENGELHARD, the TIMIRON® mother-of-pearls marketed by the company MERCK, the PRESTIGE® mica-based mother-of-pearls marketed by the company ECKART and the SUNSHINE® synthetic mica-based mother-of-pearls marketed by the company SUN CHEMICAL.

[0150] The mother-of-pearls may more particularly have a yellow, pink, red, bronze, orange, brown, gold and / or coppery color or reflection. As an illustration of the mother-of-pearls that can be used in the context of the present invention, mention may be made, in particular, of gold-colored mother-of-pearls, in particular, marketed by the company ENGELHARD, under the name Brillant gold 212G® (Timica), Gold 222C® (Cloisonne), Sparkle Gold® (Timica), Gold 4504® (Chromalite) and Monarch Gold 233X® (Cloisonne); bronze mother-of-pearls, in particular, marketed by the company MERCK under the name Bronze fine® (17384) (Colorona) and Bronze® (17353) (Colorona) and by the company ENGELHARD under the name Super bronze (Cloisonne); orange mother-of-pearls, in particular, marketed by the company ENGELHARD under the name Orange 363C® (Cloisonne) and Orange MCR 101® (Cosmica) and by the company MERCK under the name Passion Orange® (Colorona) and Matte Orange (17449) ® (Microna);brown mother-of-pearl, in particular, marketed by the company ENGELHARD under the name Nu-Antique Copper 340XB® (Cloisonne) and Brown CL4509® (Chromalite); copper-reflecting mother-of-pearl, in particular, marketed by the company ENGELHARD under the name Copper 340A® (Timica); red-reflecting mother-of-pearl, in particular, marketed by the company MERCK under the name Sienna Fine® (17386) (Colorona); yellow-reflecting mother-of-pearl, in particular, marketed by the company ENGELHARD under the name Yellow (4502) ® (Chromalite); red-reflecting mother-of-pearl with a gold sheen, in particular, marketed by the company ENGELHARD under the name Sunstone G012® (Gemtone); pink mother-of-pearl, in particular, marketed by the company ENGELHARD under the name Tan Opale G005® (Gemtone);black mother-of-pearl with a gold sheen, in particular, marketed by the company ENGELHARD under the name Nu Antique Bronze 240 AB® (Timica), blue mother-of-pearl, in particular, marketed by the company MERCK under the name Matte Blue® (17433) (Microna), white mother-of-pearl with a sheen; silver, in particular, marketed by the company MERCK under the name Xirona Silver® and the orange-pinkish-green-gold mother-of-pearl, in particular, marketed by the company MERCK under the name Indian Summer® (Xirona) and their mixtures.

[0151] Among the pigments which can be used according to the invention, mention may also be made of those with an optical effect different from a simple conventional tint effect, that is to say unified and stabilized as produced by conventional coloring materials, such as, for example, monochromatic pigments. For the purposes of the invention, "stabilized" means devoid of any effect of color variability with the viewing angle or in response to a change in temperature. For example, this material may be chosen from particles with a metallic sheen, goniochromatic coloring agents, diffracting pigments, thermochromic agents, optical brightening agents, as well as fibers, in particular interference fibers. Of course, these different materials may be combined so as to provide the simultaneous manifestation of two effects, or even a new effect in accordance with the invention.

[0152] The particles with a metallic sheen that can be used in the invention are in particular chosen from:

[0153] - particles of at least one metal and / or at least one metal derivative,

[0154] - particles comprising an organic or mineral substrate, single-material or multi- materials, covered at least partially by at least one layer with a metallic sheen comprising at least one metal and / or at least one metallic derivative, and

[0155] - mixtures of said particles.

[0156] Among the metals that may be present in said particles, there may be mentioned for example Ag, Au, Cu, Al, Ni, Sn, Mg, Cr, Mo, Ti, Zr, Pt, Va, Rb, W, Zn, Ge, Te, Se and their mixtures or alloys. Ag, Au, Cu, Al, Zn, Ni, Mo, Cr, and their mixtures or alloys (for example, bronzes and brasses) are preferred metals.

[0157] By metal derivatives, we mean compounds derived from metals, in particular, oxides, fluorides, chlorides and sulfides.

[0158] As an illustration of these particles, mention may be made of aluminum particles, such as those marketed under the names STARBRITE 1200 EAC® by the company SIBERLINE and METALURE® by the company ECKART.

[0159] Mention may also be made of metallic copper powders or mixtures of alloys, such as the references 2844 marketed by the company RADIUM BRONZE, metallic pigments, such as aluminum or bronze, such as those marketed under the names ROTOSAFE 700® from the company ECKART, particles of aluminum coated with silica marketed under the name VI-SIONAIRE BRIGHT SILVER® from the company ECKART and particles of metallic alloy, such as bronze powders (copper and zinc alloy) coated with silica marketed under the name Visionaire Bright Natural Gold® from the Eckart company.

[0160] It may also be a question of particles comprising a glass substrate such as those marketed by the company NIPPON SHEET GLASS under the name ML CROGLASS METASHINE®.

[0161] The goniochromatic coloring agent may be selected, for example, from interference multilayer structures and liquid crystal coloring agents.

[0162] Examples of symmetrical interference multilayer structures that can be used in compositions produced in accordance with the invention are, for example, the following structures: Al / SiO2 / Al / SiO2 / Al, pigments having this structure being marketed by the company DUPONT DE NEMOURS; Cr / MgF2 / Al / MgF2 / Cr, pigments having this structure being marketed under the name CHROMAFLAIR® by the company FLEX; MoS2 / SiO2 / Al / SiO2 / MoS2; Fe2O3 / SiO2 / Al / SiO2 / Fe2O3, and Fe2O3 / SiO2 / Fe2O3 / SiO2 / Fe2O3, pigments having these structures being marketed under the name SICOPEARL® by the company BASF; MoS2 / SiO2 / mica-oxide / SiO2 / MoS 2 ; Fe2O3 / SiO2 / mica-oxide / SiO2 / Fe2O3; TiO2 / SiO2 / TiO2 and TiO2 / Al2O3 / TiO2; SnO / TiO2 / SiO2 / TiO2 / SnO; Fe2O3 / SiO2 / Fe2O3; SnO / mica / TiO2 / SiO2 / TiO2 / mica / SnO, pigments having these structures being marketed under the name XIRONA® by the company MERCK (Darmstadt).For example, these pigments may be the silica / titanium oxide / tin oxide structure pigments marketed under the name XIRONA MAGIC® by MERCK, the silica / brown iron oxide structure pigments marketed under the name XIRONA INDIAN SUMMER® by MERCK and the silica / titanium oxide / mica / tin oxide structure pigments marketed under the name XIRONA CARRIBEAN BLUE® by MERCK. Mention may also be made of the INFINITE COLORS pigments from SHISEIDO. Depending on the thickness and nature of the different layers, different effects are obtained. Thus, with the Fe2O3 / SiO2 / Al / SiO2 / Fe2O3 structure, the color goes from gold-green to gray-red for SiO2 layers of 320 to 350 nm; from red to gold for SiO2 layers of 380 to 400 nm; from violet to green for SiO2 layers from 410 to 420 nm; from copper to red for SiO2 layers from 430 to 440 nm.

[0163] Examples of pigments with a polymeric multilayer structure include those marketed by the company 3M under the name COLOR GLITTER®.

[0164] As liquid crystal goniochromatic particles, it is possible to use, for example, those sold by the company CHENIX, as well as those marketed under the name HELICONE® HC by the company WACKER. Hydrophobic coated pigments

[0165] According to a particular embodiment of the invention, the compositions according to the invention comprise at least one pigment coated with at least one lipophilic or hy- drophobe and in particular as detailed below.

[0166] This type of pigment is particularly advantageous insofar as it can be considered in significant quantity together with a significant quantity of water. What is more, insofar as they are treated with a hydrophobic compound, they show a preponderant affinity for the oily gelled phase which can then transport them.

[0167] Of course, the compositions according to the invention can at the same time contain uncoated pigments.

[0168] The coating may also comprise at least one additional non-lipophilic compound.

[0169] For the purposes of the invention, the coating of a pigment according to the invention generally designates the total or partial surface treatment of the pigment by a surface agent, absorbed, adsorbed or grafted onto said pigment.

[0170] The surface-treated pigments may be prepared according to surface treatment techniques of a chemical, electronic, mechanochemical or mechanical nature well known to those skilled in the art. Commercial products may also be used.

[0171] The surfactant can be absorbed, adsorbed or grafted onto the pigments by solvent evaporation, chemical reaction and creation of a covalent bond.

[0172] According to one variant, the surface treatment consists of a coating of the pigments.

[0173] The coating may represent from 0.1% to 20% by weight, and in particular from 0.5% to 5% by weight. % by weight of the total weight of the coated pigment.

[0174] The coating can be carried out for example by adsorption of a liquid surface agent on the surface of the solid particles by simple mixing with stirring of the particles and said surface agent, possibly hot, prior to the incorporation of the particles into the other ingredients of the makeup or care composition.

[0175] The coating can be carried out for example by chemical reaction of a surfactant with the surface of the solid pigment particles and creation of a covalent bond between the surfactant and the particles. This method is notably described in US patent 4,578,266.

[0176] The chemical surface treatment may consist of diluting the surfactant in a volatile solvent, dispersing the pigments in this mixture, and then slowly evaporating the volatile solvent, so that the surfactant is deposited on the surface of the pigments. Lipophilic or hydrophobic treatment agent

[0177] When the pigment comprises a lipophilic or hydrophobic coating, the latter is preferably present in the fatty phase of the composition according to the invention.

[0178] According to a particular embodiment of the invention, the pigments can be coated according to the invention with at least one compound chosen from surface agents silicones; fluorinated surfactants; fluoro-silicone surfactants; metallic soaps; N-acylated amino acids or their salts; lecithin and its derivatives; isopropyl triisostearyl titanate; isostearyl sebacate; natural vegetable or animal waxes; polar synthetic waxes; fatty esters; phospholipids; and mixtures thereof. Silicone surfactant

[0179] According to a particular embodiment, the pigments can be surface-treated totally or partially with a silicone compound.

[0180] The silicone surfactants may be chosen from organopolysiloxanes, silane derivatives, silicone-acrylate copolymers, silicone resins, and mixtures thereof.

[0181] By organopolysiloxane compound is meant a compound having a structure comprising alternating silicone atoms and oxygen atoms and comprising organic radicals linked to the silicon atoms. Non-elastomeric organopolysiloxane

[0182] Non-elastomeric organopolysiloxanes that may be mentioned include polydimethylsiloxanes, polymethylhydrogensiloxanes and polyalkoxydimethylsiloxanes.

[0183] The alkoxy group may be represented by the radical RO- such that R represents methyl, ethyl, propyl, butyl or octyl, 2-phenylethyl, 2-phenylpropyl or 3,3,3-trifluoropropyl radicals, aryl radicals such as phenyl, tolyl, xylyl, or substituted aryl radicals such as phenylethyl.

[0184] One method for surface-treating pigments with polymethylhydrogenosiloxane involves dispersing the pigments in an organic solvent and then adding the silicone compound. By heating the mixture, covalent bonds are created between the silicone compound and the surface of the pigment.

[0185] According to a preferred embodiment, the silicone surfactant may be a non-elastomeric organopolysiloxane, in particular chosen from polydimethylsiloxanes. Alkylsilanes and alkoxysilanes

[0186] Alkoxy-functional silanes are notably described by Witucki in A silane primer, Chemistry and applications of alkoxysilanes, Journal of Coatings Technology, 65, 822, pages 57-60, 1993.

[0187] Alkoxysilanes such as alkyltriethoxysilanes and alkyltrimethoxysilanes marketed under the references Milquet A-137® (OSI Specialities) and Prosil 9202® (PCR) can be used for coating pigments.

[0188] The use of alkylpolysiloxanes having a reactive terminal group such as alkoxy, hydroxy, halogen, amino or imino are described in the application JP H07-196946. They are also suitable for processing pigments. Silicone-acrylate polymers

[0189] Grafted silicone-acrylic polymers having a silicone backbone as described in US patents 5,725,882, US 5,209,924, US 4,972,037, US 4,981,903, US 4,981,902, US 5,468,477, and in patents US 5,219,560 and EP 0 388 582, can be used.

[0190] Other silicone-acrylate polymers may be silicone polymers comprising in their structure the following unit of formula (II):

[0191] [Chem. 11] G.^ .............( ““ S ] O .............( ““ S § ~ O " )............( S ï —“ O ............ (G.)- G. (II)

[0192] in which the radicals Gi, identical or different, represent hydrogen or a C1-C10 alkyl radical or a phenyl radical; the radicals G2, identical or different, represent a C1-C10 alkylene group; G3 represents a polymeric residue resulting from the (homo)polymerization of at least one anionic monomer with ethylenic unsaturation; G4 represents a polymeric residue resulting from the (homo)polymerization of at least one hydrophobic monomer with ethylenic unsaturation; m and n are equal to 0 or 1; a is an integer ranging from 0 to 50; b is an integer which can be between 10 and 350, it is an integer ranging from 0 to 50, provided that one of the parameters a and c is different from 0.

[0193] Preferably, the unit of formula (II) above has at least one, and even more preferably all, of the following characteristics:

[0194] - the radicals Gi denote an alkyl radical, preferably the methyl radical;

[0195] -n is non-zero, and the radicals G2 represent a divalent radical in C1-C3, preferably a propylene radical;

[0196] -G3 represents a polymeric radical resulting from the (homo)polymerization of at at least one monomer of the ethylenically unsaturated carboxylic acid type, preferably acrylic acid and / or methacrylic acid;

[0197] - G4 represents a polymeric radical resulting from the (homo)polymerization of at at least one monomer of the (Ci-Cio)alkyl (meth)acrylate type, preferably of the isobutyl or methyl (meth)acrylate type.

[0198] Examples of silicone polymers corresponding to formula (II) are in particular polydimethylsiloxanes (PDMS) onto which are grafted, via a connecting link of the thiopropylene type, mixed polymer units of the type poly(meth)acrylic acid and poly(methyl meth)acrylate type.

[0199] Other examples of silicone polymers corresponding to formula (II) are in particular polydimethylsiloxanes (PDMS) onto which are grafted, via a connecting link of the thiopropylene type, polymer units of the isobutyl poly(meth)acrylate type. Silicone resins

[0200] The silicone surfactant may be chosen from silicone resins. Fluorinated surfactant

[0201] The pigments can be surface treated totally or partially with a compound of a fluorinated nature.

[0202] The fluorinated surfactants may be chosen from perfluoroalkyl phosphates, perfluoropoly ethers, polytetrafluoropolyethylenes (PTFE), perfluoroalkanes, perfluoroalkyl silazanes, hexafluoropropylene polyoxides, polyorganosiloxanes comprising perfluoroalkyl perfluoropoly ether groups.

[0203] The term perfluoroalkyl radical means an alkyl radical in which all the hydrogen atoms have been replaced by fluorine atoms.

[0204] Perfluoropolyethers are notably described in patent application EP 0 486 135, and sold under the trade names FOMBLIN by the company MONTEFLUOS.

[0205] Perfluoroalkyl phosphates are in particular described in application JP H05-86984. The perfluoroalkyl phosphate-diethanol amine marketed by Asahi Glass under the reference Asahi Guard AG530® can be used.

[0206] Among the linear perfluoroalkanes, mention may be made of perfluorocycloalkanes, perfluoro(alkylcycloalkanes), perfluoropolycycloalkanes, aromatic perfluorohydrocarbons (perfluoroarenes) and organoperfluorinated hydrocarbon compounds comprising at least one heteroatom.

[0207] Among the perfluoroalkanes, mention may be made of the series of linear alkanes such as perfluorooctane, perfluorononane or perfluorodecane.

[0208] Among the perfluorocycloalkanes and perfluoro(alkylcycloalkanes), mention may be made of perfluorodecalin sold under the name FLUTEC PP5 GMP by the company RHODIA, perfluoro(methyldecalin), perfluoro(C3-C5)alkyl-cyclohexanes) such as perfluoro(butylcyclohexane).

[0209] Among the perfluoropolycycloalkanes, mention may be made of bicyclo[3.3.1]nonane derivatives such as perfluorotrimethylbicyclo[3.3.1]nonane, adamantane derivatives such as perfluorodimethyladamantane and perfluorinated derivatives of hydrogenated phenanthrene such as tetracosafluoro-tetradecahydrophenanthrene.

[0210] Among the perfluoroarenes, we can cite perfluorinated derivatives of naphthalene such as perfluoronaphthalene and perfluoromethyl-l-naphthalene.

[0211] As examples of commercial references of pigments treated with a fluorinated compound, we can cite:

[0212] - yellow iron oxide / perfluoroalkyl phosphate sold under the reference PF 5 Yellow 601® by the Daito Kasei company;

[0213] - red iron oxide / perfluoroalkyl phosphate sold under the reference PF 5 Red R 516L® by Daito Kasei Company;

[0214] -black iron oxide / perfluoroalkyl phosphate sold under the reference PF 5 Black BL 100® by the company Daito Kasei;

[0215] - titanium dioxide / perfluoroalkyl phosphate sold under the reference PF 5 TiO2 CR 50® by Daito Kasei company;

[0216] -yellow iron oxide / perfluoropolymethylisopropylether sold under the reference Iron Oxide Yellow BF-25-3® by the company Toshiki;

[0217] - DC Red 7 / perfluoropolymethylisopropylether sold under the reference D&C Red 7 FHC® by Cardre Inc.; and

[0218] - DC Red 6 / PTFE sold under the reference T 9506® by the company Wamer- Jenkinson. Fluorosilicone surfactant

[0219] The pigments can be surface treated totally or partially with a compound of a fluoro-silicone nature.

[0220] The fluoro-silicone compound may be chosen from perfluoroalkyl dimethicones, perfluoroalkyl silanes and perfluoroalkyltrialkoxysilanes.

[0221] Examples of perfluoroalkyl silanes that may be mentioned are the products LP-IT® and LP-4T® marketed by Shin-Etsu Silicone.

[0222] As an example of commercial references of pigment treated with a fluoro-silicon compound, mention may be made of titanium dioxide / fluorosilicone sold under the reference Fluorosil Titanium Dioxide 100TA® by the company Advanced Dermaceuticals International Inc. Other lipophilic surfactants

[0223] The hydrophobic treatment agent may also be chosen from

[0224] (i) metallic soaps such as aluminum dimyristate, and aluminum salt hydrogenated tallow glutamate.

[0225] As metallic soaps, mention may in particular be made of metallic soaps of fatty acids having from 12 to 22 carbon atoms, and in particular those having from 12 to 18 carbon atoms.

[0226] The metal in the metallic soap may in particular be zinc or magnesium.

[0227] As metallic soap, zinc laurate, stearate of magnesium, magnesium myristate, zinc stearate, and mixtures thereof.

[0228] The hydrophobic treatment agent may also be chosen from ii) fatty acids such as lauric acid, myristic acid, stearic acid, palmitic acid.

[0229] The hydrophobic treatment agent may also be chosen from iii) N-acylated amino acids or their salts which may comprise an acyl group having from 8 to 22 carbon atoms, such as for example a 2-ethyl hexanoyl, caproyl, lauroyl, myristoyl, palmitoyl, stearoyl, cocoyl group.

[0230] The amino acid may be, for example, lysine, glutamic acid or alanine.

[0231] The salts of these compounds can be the salts of aluminum, magnesium, calcium, zirconium, zinc, sodium, potassium.

[0232] Thus, according to a particularly preferred embodiment, an N-acylated amino acid derivative may in particular be a glutamic acid derivative and / or one of its salts, and more particularly a stearoyl glutamate, such as for example aluminum stearoyl glutamate.

[0233] The hydrophobic treatment agent may also be chosen from iv) lecithin and its derivatives.

[0234] The hydrophobic treatment agent may also be v) isopropyl triisostearyl titanate.

[0235] Examples of pigments treated with isopropyl titanium triisostearate (ITT) include those sold under the commercial reference BWB0-I2® (Iron oxide CI77499 and isopropyl titanium triisostearate), BWY0-I2® (Iron oxide CI77492 and isopropyl titanium triisostearate), and BWR0-I2® (Iron oxide CI77491 and isopropyl titanium triisostearate) by the company KOBO.

[0236] The hydrophobic treatment agent may also be vi) isostearyl sebacate.

[0237] The hydrophobic treatment agent may also be chosen from vii) na waxes vegetable or animal oils or polar synthetic waxes.

[0238] The hydrophobic treatment agent may also be chosen from viii) fatty esters, in particular jojoba esters.

[0239] The hydrophobic treatment agent may also be chosen from ix) phospholipids.

[0240] The waxes mentioned in the compounds cited above may be those generally used in the cosmetic field, as defined below.

[0241] They may in particular be hydrocarbon-based, silicone-based and / or fluorinated, possibly comprising ester or hydroxyl functions. They may also be of natural or synthetic origin.

[0242] Polar wax is understood to mean a wax containing chemical compounds comprising at least one polar group. Polar groups are well known to those skilled in the art; they may be, for example, alcohol, ester, carbon acid groups. carboxylic. Polar waxes do not include polyethylene waxes, paraffin waxes, microcrystalline waxes, ozokerite, or Fisher-Tropsch waxes.

[0243] In particular, polar waxes have an average HANSEN solubility parameter ôa at 25°C such that ôa > 0 (J / cm3)1 / 2 and better ôa > 1 (J / cm3)1 / 2:

[0244] [Math.l] ô ~ 4 dr

[0245] where ôp and ôh are respectively the polar and interaction-type contributions specific to the Hansen solubility parameters.

[0246] The definition of solvents in the three-dimensional solubility space according to HANSEN is described in the article by CM HANSEN, The three dimensional solubility parameters J. Paint Technol. 39, 105 (1967):

[0247] - ôh characterizes the specific interaction forces (hydrogen bond type, acid / base, donor / acceptor, etc.);

[0248] - ôp characterizes the DEBYE interaction forces between permanent dipoles as well than the KEESOM interaction forces between induced dipoles and permanent dipoles.

[0249] The parameters ôp and ôh are expressed in (J / cm3)1 / 2.

[0250] A polar wax is in particular made up of molecules comprising, in addition to carbon and hydrogen atoms in their chemical structure, heteroatoms (such as O, N, P).

[0251] By way of illustration and not limitation of these polar waxes, mention may in particular be made of natural polar waxes, such as beeswax, lanolin wax, orange wax, lemon wax, and Chinese insect waxes, rice bran wax, Carnauba wax, Candellila wax, Ouricury wax, cork fiber wax, sugar cane wax, Japanese wax and sumac wax, montan wax.

[0252] According to a particular embodiment, the pigments can be coated with at least one compound chosen from silicone surfactants; fluorinated surfactants; N-acylated amino acids or their salts; isopropyl trisostearyl titanate; natural vegetable or animal waxes; fatty esters; and mixtures thereof.

[0253] According to a particularly preferred embodiment, the pigments may be coated with an N-acylated amino acid and / or one of its salts, in particular with a glutamic acid derivative and / or one of its salts, or with a fatty ester, in particular with a jojoba ester.

[0254] According to a more particularly preferred embodiment, the pigments may be coated with an N-acylated amino acid and / or one of its salts, in particular with a glutamic acid derivative and / or one of its salts, in particular a stearoyl glutamate, such as for example aluminum stearoyl glutamate.

[0255] As examples of coated pigments according to the invention, mention may be made more particularly of titanium dioxides and iron oxides, coated with aluminum stearoyl glutamate, for example marketed under the reference NAI by MIYOSHI KASEI. Pigments not coated with a hydrophobic compound

[0256] As stated previously, a composition may further contain pigments not coated with a lipophilic or hydrophobic compound.

[0257] These other pigments may be coated with a hydrophilic compound or uncoated.

[0258] These pigments may be mineral pigments, in particular as defined above.

[0259] These pigments can also be organic pigments.

[0260] By organic pigment is meant any pigment which meets the definition of the Ullmann encyclopedia in the organic pigment chapter. The organic pigment may in particular be chosen from nitroso, nitro, azo, xanthene, quinoline, anthraquinone, phthalocyanine, metal complex type compounds, isoindolinone, isoindoline, quinacridone, perinone, perylene, diketopyrrolopyrrole, thioindigo, dioxazine, triphenylmethane, quinophthalone.

[0261] 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, 74160, the yellow pigments codified in the Color Index under the references CI 11680, 11710, 15985, 19140, 20040, 21100, 21108, 47000, 47005, the green pigments codified in the Color Index under the references CI 61565, 61570, 74260, the orange pigments codified in the Color Index under the references CI 11725, 15510, 45370, 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, 75470, and the pigments obtained by oxidative polymerization of indole derivatives,phenolics as described in patent FR 2 679 771.,

[0262] These pigments can also be in the form of composite pigments as described in patent EPI 184426. These composite pigments can be composed in particular of particles comprising an inorganic core covered at least partially with an organic pigment and at least one binder ensuring the fixing of the organic pigments on the core.

[0263] The pigment may also be a lake. By lake is meant insolubilized dyes adsorbed on insoluble particles, the whole thus obtained remaining insoluble during use.

[0264] The inorganic substrates on which the dyes are adsorbed are, for example, alumina, silica, calcium and sodium borosilicate or calcium and aluminum borosilicate, and aluminum.

[0265] Among the organic dyes, we can cite cochineal carmine. Other products known under the following names include: 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).

[0266] Examples of lacquers include the product known under the name D&C Red 7 (CI 15 850:1). Nature of the hydrophilic coating

[0267] As stated previously, these other pigments can be coated with a hydrophilic compound.

[0268] Said hydrophilic compound for treating a pigment on the surface to optimize its dispersion in the gelled aqueous phase is more particularly chosen from biological polymers, carbohydrates, polysaccharides, polyacrylates or polyethylene glycol derivatives.

[0269] Examples of biological polymers include polymers based on carbohydrate-type monomers.

[0270] More particularly, mention may be made of biosaccharide gum; chitosans and their derivatives, such as butoxychitosan, carboxymethyl chitosan, carboxybutyl chitosan, chitosan gluconate, chitosan adipate, chitosan glycolate, chitosan lactate, etc.; chitins and their derivatives, such as carboxymethyl chitin, chitin glycolate; cellulose and its derivatives such as cellulose acetate; microcrystalline cellulose; distarch phosphate; sodium hyaluronate; soluble proteoglycans; galacto-arabinans; glycosaminoglycans; glycogen; Sclerotium gum; dextran; starch and its derivatives; and mixtures thereof.

[0271] Examples of carbohydrates that may be mentioned include polyhydroxy-aldehydes or polyhydroxyketones, of general formula: Cx(H2O)y

[0272] in which x and y can range from 1 to 1,000,000.

[0273] Carbohydrates can be monosaccharides, disaccharides or polysaccharides.

[0274] Examples of carbohydrates that may be mentioned include amylodextrins, betaglucans, cyclodextrins, modified corn starch, glycogen, hyaluronic acid, luronic acid, hydroxypropylcyclodextrin, lactose, maltitol, guanosine, glyceryl starch, Triticum Vulgare starch, trehalose, sucrose and its derivatives, raffinose, sodium chondridine sulfate.

[0275] Also suitable as surface treatment agents are C1-C2o alkylene glycols or C1-C20 alkylene glycol ethers, alone or used in combination with tri-C1-C2o-alkylsilanes.

[0276] Examples that may be mentioned are pigments surface-treated with PEG alkyl ether alkoxy silane, such as, for example, pigments treated with PEG-8-methyl ether triethoxysilane marketed by the company KOBO under the name SW pigments.

[0277] Also suitable for the invention as surface treatment agent are silicones such as dimethicones having hydrophilic groups, also known as dimethicone copolyols or alkyl dimethicone copolyols. In particular, such dimethicones may comprise, as repeating units, C1-C20 alkylene oxides, such as ethylenic or propylenic.

[0278] As an example, mention may be made of the pigment treated with PEG-12-Dimethicone, marketed by the company SENSIENT CORPORATION, under the name LCW AQ® Pigment.

[0279] The quantity of pigments coated with at least one hydrophilic compound and / or uncoated pigments is in particular conditioned by the destination of the cosmetic composition considered and its adjustment is of course within the competence of the formulator of the composition.

[0280] According to a particular embodiment, the composition additionally comprises at least one pigment chosen from titanium dioxides and / or iron oxides, in particular coated with a hydrophobic surface treatment agent, in particular with an N-acylated amino acid and / or one of its salts, in particular with a glutamic acid derivative and / or one of its salts, in particular a stearoyl glutamate, such as for example aluminum stearoyl glutamate.

[0281] According to a particular embodiment, the composition according to the invention comprises at least one uncoated or coated pigment, preferably at least one coated pigment. Alpha hydroxy acid (AHA)

[0282] The composition according to the invention may comprise at least one AHA.

[0283] By alpha hydroxy acid is meant according to the present invention a carboxylic acid having at least one hydroxy function occupying an alpha position on said acid (carbon adjacent to a carboxylic acid function). This acid can be present in the final composition in the form of free acid and / or in the form of one of its associated salts (salts with an organic base or an alkali in particular), in particular according to the final pH imposed on the composition.

[0284] The α-hydroxy acids (alpha hydroxy acids or AHAs) are, for example, chosen from lactic acid, citric acid, methyllactic acid, glucuronic acid, glycolic acid, pyruvic acid, 2-hydroxybutanoic acid, 2-hydroxypentanoic acid, 2-hydroxyhexanoic acid, 2-hydroxyheptanoic acid, 2-hydroxyoctanoic acid, 2-hydroxynonanoic acid, 2-hydroxydecanoic acid, 2-hydroxyundecanoic acid, 2-hydroxydodecanoic acid, 2-hydroxytetradecanoic acid, 2-hydroxyhexadecanoic acid, 2-hydroxyoctadecanoic acid, 2-hydroxytetracosanoic acid, 2-hydroxyeicosanoic acid; mandelic acid; phenyllactic acid; gluconic acid; galacturonic acid; aleuritic acid; ribonic acid; tartronic acid; tartaric acid; malic acid; fumaric acid; their salts and mixtures thereof.

[0285] According to a preferred embodiment, the alpha hydroxy acid is chosen from lactic acid, citric acid, malic acid, tartaric acid and their salts. More particularly, the alpha hydroxy acid is chosen from lactic acid, citric acid, their salts and their mixtures.

[0286] The alpha hydroxy acid(s) may be present in an amount ranging from 0.001 to 10% by weight, from 0.005 to 5% by weight, preferably from 0.01 to 3% by weight relative to the total weight of the composition. Surfactant

[0287] The composition may also comprise at least one surfactant, preferably non-ionic, cationic or anionic, preferentially a non-ionic surfactant.

[0288] Preferably, the non-ionic surfactant may be chosen from non-ionic surfactants known from the prior art, in particular from fatty acid and polyglycerol esters, sugar esters, poloxamers, polysorbates and mixtures thereof.

[0289] Preferably, the non-ionic surfactant is chosen from fatty acid and polyglycerol esters and sugar esters, preferentially from fatty acid and polyglycerol esters.

[0290] When present, the non-ionic surfactant(s) is (are) present in a content of between 0.01% and 15% by weight, preferably in a content of between 0.05% and 10% by weight, preferably between 0.1% and 8% by weight, preferably between 1% and 7% by weight relative to the total weight of the composition. Physiologically acceptable aqueous medium

[0291] The composition according to the invention comprises a physiologically acceptable aqueous medium. Said medium comprises water.

[0292] The water used may be sterile demineralized water and / or a floral water such as rose water, cornflower water, chamomile water or linden water, and / or a natural thermal or mineral water such as VITTEL water, LUCAS water or LA ROCHE POSAY water.

[0293] The composition preferably comprises at least 5% by weight of water relative to the total weight of the composition, preferably at least 10% by weight, preferably at least 20% by weight, preferably at least 25% by weight, preferably at least 30% by weight, preferably at least 35% by weight, preferably at least 40% by weight, preferably at least 50% by weight, more preferably at least 60% by weight, even more preferably at least 70% by weight, advantageously at least 80% by weight.

[0294] The composition preferably comprises from 5% to 95% by weight of water relative to the total weight of the composition, more preferably from 10% to 85%, even more preferably from 20% to 80%, even more preferably from 25% to 75%, even more preferably from 28% to 70%, even more preferably from 30% to 65%, even more preferably from 35% to 60%.

[0295] The aqueous phase may also comprise at least one organic solvent miscible in water at 25°C.

[0296] Preferably, the water-miscible organic solvent is chosen from alcohols, polyols and their mixtures.

[0297] Among the alcohols, mention may be made of C1-C10 alcohols, more preferably C1-C5, such as ethanol, isopropanol, propanol and butanol.

[0298] The polyol is preferably chosen from polyols having from 2 to 20 carbon atoms, more preferably from 2 to 6 carbon atoms, such as glycerol, diglycerol, propylene glycol, isoprene glycol, dipropylene glycol, butylene glycol, hexylene glycol, 1,2-propanediol, 1,3-propanediol, pentylene glycol, polyethylene glycols having from 2 to 200 ethylene oxide units and mixtures thereof.

[0299] The composition may comprise from 0.1% to 25% by weight of water-miscible organic solvent, relative to the total weight of the composition, more preferably from 0.5% to 20% by weight, more preferably from 1% to 15% by weight, more preferably from 1.5% to 10% by weight, even more preferably from 2% to 5% by weight.

[0300] Preferably, the weight ratio between the polyol(s), if present, and the chitosan (i.e. polyol(s): chitosan weight ratio) is between 0.1 and 6. Preferably, it is between 0.1 and 5, preferably between 0.2 and 5, preferably between 0.2 and 4.5, preferably between 0.5 and 2. Oily phase

[0301] The composition according to the invention preferably also comprises at least one oily phase. When the composition used according to the invention comprises an oily phase, the latter preferably contains at least one oil, in particular an oil cosmetic. It may also contain other fatty substances.

[0302] By “oil” is meant a non-aqueous compound, liquid at 25°C and atmospheric pressure (1,013.105 Pa), immiscible with water.

[0303] By "immiscible" is meant that the mixture of the same quantity of water and oil, after stirring, does not lead to a stable solution comprising only one phase, under the aforementioned temperature and pressure conditions. The observation is made by eye or by means of a phase contrast microscope if necessary, on 100g of mixture obtained after Rayneri stirring sufficient to cause a vortex to appear within the mixture (for information 200 to 1000 rpm); the resulting mixture being left to stand, in a closed bottle, for 24 hours at room temperature before observation.

[0304] As oils which can be used in the composition of the invention, we can cite for example:

[0305] - hydrocarbon oils of animal origin, such as perhydrosqualene;

[0306] - hydrocarbon oils of vegetable origin, such as liquid triglycerides fatty acids containing 4 to 10 carbon atoms such as triglycerides of heptanoic or octanoic acids or, for example, sunflower, corn, soybean, pumpkin, grape seed, sesame, hazelnut, apricot, macadamia, arara, sunflower, castor, avocado oils, triglycerides of caprylic / capric acids such as those sold by the company Stearineries Dubois or those sold under the names Miglyol 810, 812 and 818 by the company Dynamit Nobel, jojoba oil, shea butter oil;

[0307] - synthetic esters and ethers, in particular of fatty acids, such as oils of formulas R1COOR2 and R1OR2 in which RI represents the residue of a fatty acid containing from 8 to 29 carbon atoms, and R2 represents a hydrocarbon chain, branched or not, containing from 3 to 30 carbon atoms, such as for example Purcellin oil, isononyl isononanoate, isopropyl myristate, 2-ethylhexyl palmitate, 2-octyldodecyl stearate, 2-octyldodecyl erucate, isostearyl isostearate; hydroxylated esters such as isostearyl lactate, octylhydroxystearate, octyldodecyl hydroxystearate, diisostearylmalate, triisocetyl citrate, fatty alcohol heptanoates, octanoates, decanoates; polyol esters, such as propylene glycol dioctanoate, neopentyl glycol diheptanoate and diethylene glycol diisononanoate; and pentaerythritol esters such as pentaerythrityl tetraisostearate or dipentaerythrityl pentaisononanoate;

[0308] - linear or branched hydrocarbons, of mineral or synthetic origin, such as paraffin oils, volatile or not, and their derivatives, branched-chain hydrocarbon oils containing 10 to 20 carbon atoms such as isohexadecane, isododecane, isoparaffins and their mixtures, petroleum jelly, polydecenes, polyisobutenes, hydrogenated polyisobutenes such as, for example, Parléam® marketed by NIPPON OIL FATS, PANALANE H-300 E marketed by AMOCO, VISEAL 20000 marketed by SYNTEAL, REWOPAL PIB 1000 marketed by WITCO, or PARLEAM LITE marketed by NOF Corporation, branched alkanes alone or in mixtures, such as the mixture of undecane and tridecane marketed under the name Cetiol UT by BASF, or alkanes of plant origin, in particular coconut, such as those marketed under the name VEGELIGHT SILK by BIOSYNTHIS, or the mixture of C13-15 alkanes marketed under the name NEOSSANCE HEMISQUALANE CN by AMYRIS;

[0309] - partially hydrocarbon and / or silicone fluorinated oils such as those described in document JP-A-2-295912; or

[0310] - their mixtures.

[0311] The composition may comprise from 5% to 90% by weight of oily phase, relative to the total weight of the composition, preferably from 7% to 80% by weight, more preferably from 10% to 60% by weight, advantageously from 15% to 40% by weight.

[0312] According to a preferred embodiment, the oily phase contains at least one non-volatile oil, the weight content of which is less than or equal to 40%, preferably less than or equal to 30%, preferably less than or equal to 20%, preferably less than or equal to 15%, preferably less than or equal to 10% and preferably less than or equal to 8%. Advantageously, the weight ratio between the non-volatile oil and the resin is between 0.01 and 10, preferably between 0.1 and 5, preferably between 0.2 and 3, preferably between 0.5 and 1.

[0313] By "non-volatile oil" is meant an oil remaining on keratin materials at room temperature and atmospheric pressure for at least several hours and in particular having a vapor pressure of less than 10-3 mm Hg (0.13 Pa).

[0314] The oils can be chosen from the oils mentioned above.

[0315] According to one embodiment, the composition according to the invention further comprises a volatile oil and / or a volatile alcohol.

[0316] For the purposes of the invention, the term "volatile oil" means any oil capable of evaporating on contact with the skin, at room temperature and atmospheric pressure. The volatile oils of the invention are volatile cosmetic oils, liquid at room temperature, having a non-zero vapor pressure, at room temperature and atmospheric pressure, ranging in particular from 0.13 Pa to 40,000 Pa (0.001 to 300 mm Hg) and preferably ranging from 1.3 to 1300 Pa (0.01 to 10 mm Hg).

[0317] The volatile oil may be chosen from volatile hydrocarbon oils, oils silicone volatiles, fluorinated volatile oils, and mixtures thereof, preferably among hydrocarbon volatile oils.

[0318] The volatile hydrocarbon oils may be chosen from hydrocarbon oils having from 8 to 16 carbon atoms, and in particular branched C8-C16 alkanes such as C8-C16 isoalkanes of petroleum origin (also called isoparaffins) such as isododecane (also called 2,2,4,4,6-pentamethylheptane), isodecane, isohexadecane, and for example the oils sold under the trade names Isopars® or Permethyls®.

[0319] In particular, the composition according to the invention may comprise isododecane, cyclopentasiloxane; isohexadecane or their mixture.

[0320] The composition according to the invention may comprise a volatile oil in a content ranging from 1 to 60% by weight relative to the total weight of the composition, preferably from 5 to 50% by weight, more preferably ranging from 10 to 40% by weight, and even more preferably from 15 to 25% by weight.

[0321] By volatile alcohol is meant a C1-C4 alcohol, such as for example ethanol, isopropanol, butanol, n-propanol.

[0322] The composition according to the invention may comprise a volatile alcohol in a content ranging from 0.1% to 25% by weight of water-miscible organic solvent, relative to the total weight of the composition, preferably from 0.5% to 20% by weight, more preferably from 1% to 15% by weight, even more preferably from 1.5% to 10% by weight, advantageously from 2% to 5% by weight. pH of the composition

[0323] The composition according to the invention has a pH less than or equal to 7, preferably less than or equal to 6.5, preferably less than or equal to 6.3. Advantageously, the pH of the composition is between 3 and 6.3, preferably between 4 and 6.3.

[0324] Preferably, the cosmetic composition according to the invention comprises at least one base and / or at least one acid. The base and the acid according to the invention are known and conventionally used in the cosmetic field.

[0325] The base and / or acid are notably used to adjust the final pH of the composition between 3 and 6.3.

[0326] The acid can for example be citric acid.

[0327] The base may be chosen from mineral bases such as, for example, alkali metal hydroxides, sodium hydroxide, potassium hydroxide.

[0328] Preferably, the base of the composition is an alkali metal hydroxide, preferably sodium hydroxide or potassium hydroxide.

[0329] The composition according to the invention may comprise at least one base with an active material content ranging from 0.5% to 10% by weight, relative to the total weight of the composition, in particular from 1% to 5% by weight, preferably ranging from 1% to 4% by weight. weight.

[0330] The composition in accordance with the invention can be obtained in a conventional manner by a person skilled in the art.

[0331] The following examples illustrate the invention. Unless otherwise stated, the percentages are indicated by weight relative to the total weight of the composition (%w / w). Examples Ingredients :

[0332] [Tables 1] GLYCERY L ROSINATE PROTIUM HEP- TAPHYLLUM RESIN CANDELILL A Resin III Resin II Resin I wax Melting point (Tf) °C - - - 66-71 Softening point °C 86 84-88 42 40-45 45-52 Glass transition temperature (Tg) °C 43 40-45 51 48-55 34 -

[0333] Example 1: Preparations of compositions according to the invention and comparisons with comparative compositions

[0334] Compositions B and D according to the invention, A and C and comparative E, were prepared.

[0335] Compositions B and D according to the invention contain chitosan, candelilla resin and pigments.

[0336] Comparative compositions A and C contain chitosan and pigments, but no candelilla resin.

[0337] Comparative composition E contains a resin but no chitosan.

[0338] Compositions A and B are inverse emulsions, while compositions C to E are direct emulsions.

[0339] - Protocol for spreading compositions into a film

[0340] The products are spread on a spreading bench (Elcometer 4340 Applicator) allowing you to adjust its speed and the distance over which it is spread. The bench is equipped with a suction system connected to a pump so that the support where the spreading is done does not move. Contrast cards with a black background and a white background uncoated films are used (1 byko-chart, uncoated N2A, code 2831). The spreading thickness is adjustable using the square spreader placed on the support so as to spread by leveling when the platform is switched on. Each slice of the spreader allows spreading with a different thickness ranging from 25 pm to 200 pm. The chosen thickness is 25 pm in order to get closer to an in vivo film thickness. A weight of 960 g is added on top of the spreader during spreading. The spreading speed is set to lin / sec, or 2.54 cm / s. The films are dried for 24 hours at room temperature and humidity (RH) (50% RH).

[0341] - Contrast ratio measurement protocol for objectification of coverage

[0342]

[0343] Color measurement is performed using a Konica Minolta CM-700d spectrophotometer. Contact measurement ensures the absence of light pollution.

[0344] Selected settings: Aperture 8 mm; Uncertainty: 0.04; SCI / SCE measurement; Geometry d / 8°.

[0345] The color measurements on the two backgrounds (black background FN and white background FB) make it possible to characterize the coverage of a foundation by calculating the “contrast ratio”, (CR%), i.e. YFN / YFB x 100, where YFN and YFB are respectively the luminance values ​​measured on a black background and the white background, the latter being higher the more covering the foundation is.

[0346] - Dry, water and oil resistance test protocol

[0347]

[0348] The water friction resistance test is carried out by colorimetric measurements on dry film before and after abrasion. The abrasion is carried out by fixing a strip of tissue (Chicopee® Veraclean™ Polish Plus) wetted if necessary (400 μL of water or oil in the tissue) on the spreader edge at 25 μm. The weight of 960 g is added over the spreader during abrasion. The bench speed is set at 2.54 cm / s.

[0349]

[0350] The measurement of the color before and after abrasion is done with the same spectrophotometric method as explained previously.

[0351] In order to evaluate the resistance to friction, the "Contrast Ratio" respectively before friction (CR Dry Deposition, %) and after abrasion (CR Rub Dry Deposition, %) are measured. The loss [(CR Rub Dry Deposition - CR Dry Deposition] / CR Dry Deposition] *100, in percentage, quantifies the loss of coverage and indicates the resistance of the film to friction: the lower this loss, the more resistant the film is to friction.

[0352] Each CR value therefore represents an average of 3 to 6 measurements. Results in inverse emulsion:

[0353] Compositions A and B are prepared as follows:

[0354] Preparation of the aqueous phase:

[0355] Under a deflocculating rayneri, add the chitosan by raining it onto the water. Add the lactic acid and leave for 5 min at 300 rpm.

[0356] Meanwhile, in the final beaker, mix the isododecane, caprylic / capric triglycerides, polyglyceryl-6 polyricinoleate and the resin under a deflocculating Rayneri at 250 rpm.

[0357] Slowly add the aqueous phase to the final beaker while increasing the rotation speed to 500 rpm.

[0358] Add the dry pigments then the alcohol.

[0359] The results are in Table 2.

[0360] [Tables2] Ingredients (% w / w) A Comparative (inverse emulsion) B according to the invention (inverse emulsion) Chitosan (Kiosmetin-CSH from Kitozyme) 2 2 Lactic acid 1 1 Pigments* 12.23 12.23 Candelilla resin (CANDELILLA RESIN El -JAPAN NATURAL PRODUCTS) - 5 Caprylic / capric triglycerides 3.33 3.33 Polyglycerol-6 polyricinoleate 6 6 Isododecane 32.44 27.44 Ethanol 3 3 Water qsp 100 qsp 100 Dry strength %(+ / -%) 47 (7) 61(6) Water strength %(+ / -%) 39 (10) 72 (20)

[0361] * The pigments used in the compositions are a mixture of TiO2 pigments surface-treated with stearoyl glutamate and iron oxides treated with the disodium stearoyl glutamate / aluminum hydroxide couple (NALWhite A and NAL BHP-10, NALYHP-10 and NAI-R-800HP-10 from Miyoshi Kasei)

[0362] The results show better water and dry resistance for composition B according to the invention compared to comparative composition A.

[0363] These reverse emulsion tests show that the presence of Candelilla resin significantly improves the coverage under dry rubbing or in the presence of water of a formula already containing 2% chitosan. Results in direct emulsion:

[0364] Compositions C to E are prepared as follows:

[0365] In the final beaker, under a Rayneri deflocculator, mix the surfactant and water, add the chitosan in a sprinkler then the lactic acid and leave for 5 min at 300 rpm.

[0366] Mix the resin and the isododecane then add this mixture to the aqueous phase while regularly increasing the rotation speed from 300 to 1000 rpm.

[0367] Add the dry pigments then the alcohol.

[0368] The results are in Table 3.

[0369] [Tables3] Ingredients (% w / w) C Comparative (direct emulsion) D according to the invention (direct emulsion) E Comparative (direct emulsion) Chitosan (Kiosmetin-CSH from Kitozyme) 4 2 - Lactic acid 2 1 - Pigments* 12.23 12.23 12.23 Protium heptaphyllum resin (CITROBREU - CITROLEO) - 2 4 Caprylic / capric triglycerides 3.33 3.33 3.33 Polyglycerol-10 laurate 1 1 1 Isododecane 16 16 16 Ethanol 3 3 3 Water qsp 100 qsp 100 qsp 100 Appearance Homogeneous Homogeneous Phase shift Water resistance %(+ / -%) 55 (6) 79 (9) -

[0370] * The pigments used in the compositions are a mixture of TiO2 pigments surface-treated with stearoyl glutamate and iron oxides treated with the disodium stearoyl glutamate / aluminum hydroxide couple (NAI-White A and NAL BHP-10, NALYHP-10 and NAI-R-800HP-10 from Miyoshi Kasei)

[0371] The results show better water resistance for composition D according to the invention compared to comparative composition C. Comparative composition E is phase-shifting.

Claims

Claims

1. Cosmetic composition, in particular for makeup and / or care of the skin and / or lips and / or eyelashes and / or hair, comprising, in a physiologically acceptable aqueous medium: a) at least 0.01% by weight relative to the total weight of the composition of native chitosan having a molecular weight strictly greater than 3000 Daltons, this quantity being strictly less than 15% by weight, and b) at least one natural resin.

2. Composition according to claim 1, wherein the native chitosan has a molecular weight greater than or equal to 10 kDa, preferably greater than or equal to 15 kDa, preferably greater than or equal to 20 kDa, preferably the native chitosan has a molecular weight between 10 kDa and 2 MDa, preferably between 15 kDa and 1.5 MDa, preferably between 20 kDa and 300 kDa, preferably between 20 kDa and 200 kDa.

3. Composition according to claim 1 or 2, wherein the native chitosan has a degree of acetylation of the chitosan less than or equal to 80%, preferably less than or equal to 70%, preferably less than or equal to 60%, preferably less than or equal to 50%, preferably less than or equal to 35%, preferably less than or equal to 25%, preferably less than or equal to 15%.

4. Composition according to one of the preceding claims, in which the native chitosan is a polysaccharide prepared from a fungal origin, preferably from the mycelium of a fungus of the As-comycete type, and in particular from Aspergillus niger and / or from a Basidiomycete fungus, and in particular Lentinula edodes and / or Agaricus bisporus, preferably the fungus is Aspergillus niger.

5. Composition according to one of the preceding claims, in which the native chitosan is present in an amount ranging from 0.01% to 14% by weight, preferably from 0.1% to 14% by weight, preferably from 0.1% to 12% by weight, preferably from 0.2% to 7% by weight, preferably from 0.25% to 5% by weight, preferably from 0.3 to 3% by weight, or even more preferably from 0.5 to 2% by weight relative to the total weight of the composition.

6. Composition according to one of the preceding claims, in which the natural resin comprises at least 30% by weight of the total weight of resin of terpene compounds, preferably at least 40% by weight. of terpene compounds, preferably at least 50% of terpene compounds, and even more preferably at least 60% of terpene compounds, or even better at least 70% by weight of the total weight of resin.

7. Composition according to one of the preceding claims, in which the natural resin is chosen from the following resins, alone or in a mixture: - resins extracted from vegetable waxes, preferably EUPHORBIA CERIFERA (CANDELILLA) wax extracts; - incense resins, preferably PROTIUM HEPTAPHYLLUM RESIN, or PROTIUM RESIN, or WHITE BREU RESIN; - incense resins from the Sal tree, SHOREA ROBUSTA RESIN, alone or in a mixture with one or more fatty substances preferably chosen from volatile or non-volatile oils, preferably Shorea robusta resin with sunflower seed oil, and Shorea robusta resin with octyldodecanol;and - rosins, preferably rosin acid esters such as glyceryl rosinate, glyceryl rosinate mixed with hydrogenated vegetable oil and / or castor seed oil, pentaerythrityl rosinate or hydrogenated rosinates such as hydrogenated pentaerythrityl rosinate or hydrogenated methyl rosinate.;

8. Composition according to one of the preceding claims, in which the natural resin may be present in the composition according to the invention in a content ranging from 0.1% to 40%, preferably from 0.2% to 30%, preferably from 0.8% to 22%, preferably from 1 to 20%, and more preferably from 1.2% to 15%, preferably from 1.5% to 10%, or even more preferably 2% to 8% by weight relative to the total weight of the composition.

9. Composition according to one of the preceding claims, in which the weight ratio between the chitosan and the natural resin (i.e. chitosan: natural resin weight ratio) is between 0.00025 and 150, preferably it is between 0.001 and 100, preferentially, it is between 0.01 and 50, preferably between 0.05 and 10, and even more preferentially between 0.1 and 2.

5.

10. Composition according to one of the preceding claims, further comprising at least one compound chosen from pigmentary coloring materials.

11. A composition according to claim 10, wherein the material pigment colorant is a mineral pigment chosen from titanium dioxide, iron oxides, zirconium or cerium oxides, zinc or chromium oxides, manganese violet, ultramarine blue, chromium hydrate and ferric blue, metallic powders such as aluminum powder and copper powder, pearlescent agents and monochromatic pigments.

12. A composition according to claim 10, wherein the pigmentary coloring matter is an organic pigment selected from nitroso, nitro, azo, xanthene, quinoline, anthraquinone, phthalocyanine, metal complex type, isoindolinone, isoindoline, quinacridone, perinone, perylene, diketopyrrolopyrrole, thioindigo, dioxazine, triphenylmethane, quinophthalone.

13. Composition according to one of claims 10 or 11, in which the pigmentary coloring matter is chosen from titanium dioxide, iron oxides, zirconium or cerium oxides, zinc or chromium oxides and mixtures thereof, preferably the pigment is chosen from titanium dioxide, iron oxides and mixtures thereof.

14. Composition according to one of claims 10 to 13, in which the pigmentary coloring matter is present in a content ranging from 0.5% to 70% by weight, preferably from 1% to 60% by weight, preferably from 1% to 50% by weight, preferably from 2% to 40% by weight, relative to the weight of the composition, preferably from 4% to 30% by weight, preferably from 5% to 25% by weight, preferably from 6% to 20% by weight, preferably from 8% to 18% by weight.

15. Composition according to one of the preceding claims, comprising 10% by weight or less, preferably 5% by weight or less, of silicone, relative to the total weight of the composition.

16. Composition according to one of the preceding claims which is substantially free of silicone other than a film-forming or tackifying silicone polymer; preferably the composition comprises less than 1% by weight relative to the total weight of the composition, preferably less than 0.5% by weight, preferably less than 0.3% by weight, preferentially 0.1% by weight of silicone other than a film-forming or tackifying silicone polymer, preferably the composition is completely free of silicone other than a film-forming or tackifying silicone polymer, preferentially the composition according to the invention is substantially free of silicone, advantageously the composition is completely free of silicone.

17.

18.

19.

20. Composition according to one of the preceding claims, in which the physiologically acceptable aqueous medium comprises at least 5% by weight of water relative to the total weight of the composition, preferably at least 10% by weight, preferably at least 20% by weight, preferably at least 25%, preferably at least 30% by weight, preferably at least 35% by weight, preferably at least 40% by weight; preferably from 5% to 95% by weight of water relative to the total weight of the composition, more preferably from 10% to 85%, even more preferably from 20% to 80%, even more preferably from 25% to 75%, even more preferably from 28% to 70%, even more preferably from 30% to 65%, even more preferably from 35% to 60%; and optionally at least one organic solvent miscible in water at 25°C chosen from alcohols, polyols and their mixtures, preferably the weight ratio between the polyol(s), if present, and the chitosan is between 0,1 and 6, preferably between 0.1 and 5, preferably between 0.2 and 5, preferably between 0.2 and 4.5, preferably between 0.5 and 2. Composition according to one of the preceding claims, which comprises at least one alpha hydroxy acid, preferably chosen from lactic acid, citric acid, methyllactic acid, glucuronic acid, glycolic acid, pyruvic acid, 2-hydroxybutanoic acid, 2-hydroxypentanoic acid, 2-hydroxyhexanoic acid, 2-hydroxyheptanoic acid, 2-hydroxyoctanoic acid, 2-hydroxynonanoic acid, 2-hydroxydecanoic acid, 2-hydroxyundecanoic acid, 2-hydroxydodecanoic acid, 2-hydroxytetradecanoic acid, 2-hydroxyhexadecanoic acid, 2-hydroxyoctadecanoic acid, 2-hydroxytetracosanoic acid,2-hydroxyeicosanoic acid; mandelic acid; phenyllactic acid; gluconic acid; galacturonic acid; aleuritic acid; ribonic acid; tartronic acid; tartaric acid; malic acid; fumaric acid; their salts and mixtures thereof., Composition according to one of the preceding claims, which has a pH less than or equal to 7, preferably less than or equal to 6.5, preferably less than or equal to 6.3, preferably between 3 and 6.3, preferably between 4 and 6.

3. Composition according to one of the preceding claims, which also comprises at least one oily phase, preferably the oily phase contains at least one oil, in particular a cosmetic oil; preferably the composition is a direct or inverse emulsion.

21. Composition according to any one of the preceding claims, further comprising at least one surfactant, preferably a non-ionic surfactant, preferably in a content by weight of between 0.01% and 15% by weight, preferably in a content of between 0.05% and 10% by weight, preferably between 0.1% and 5% by weight, preferentially between 0.1% and 2% by weight relative to the total weight of the composition.

22. Composition according to any one of the preceding claims, comprising at least one non-volatile oil, the weight content of which is less than or equal to 40%, preferably less than or equal to 30%, preferably less than or equal to 20%, preferably less than or equal to 15%, preferably less than or equal to 10% and preferably less than or equal to 8% and / or the weight ratio of which between the non-volatile oil and the resin is between 0.01 and 10, preferably between 0.1 and 5, preferably between 0.2 and 3, preferably between 0.5 and 1.

23. A composition according to any preceding claim, further comprising a volatile oil and / or a volatile alcohol.

24. Method for making up and / or caring for the skin and / or the appendages, in which the composition according to one of the preceding claims is applied to the skin and / or the appendages.