Cosmetic composition for application to the skin, lips and/or nails.
Abstract
La présente invention concerne une composition présentant un pouvoir couvrant compris entre environ 25 et environ 100, et destinée à être appliquée sur la peau, les lèvres et/ou les phanères, cette composition comportant des particules d'au moins un pigment composite, ces particules comportant : un noyau inorganique,au moins un enrobage au moins partiel d'au moins une matière colorante organique dans une quantité suffisante pour que la saturation C* de la composition soit comprise entre environ 25 et environ 100.

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50 claims: 40 independent, 10 dependent
- 1Composition having a covering power of between approximately 25 and approximately 100, in particular between 25 and 90, and intended to be applied to the skin, the lips and / or the integuments, this composition comprising particles of at least one composite pigment, these particles comprising:- an inorganic nucleus, - At least one at least partial coating of at least one organic coloring matter in an amount sufficient for the saturation C * of the composition to be between approximately 25 and approximately 100.
- 3Composition according to any one of the preceding claims, characterized by the fact that the composite pigment comprises an amount of organic coloring matter sufficient for the saturation C * of the composition to be between 30 and 100.
- 4Composition according to any one of the preceding claims, characterized by the fact that the content of composite pigment in the composition is between approximately 0.1% and approximately 30% by weight relative to the total weight of the composition.
- 5Composition according to the preceding claim, characterized by the fact that the content of composite pigment in the composition is between approximately 0.1% and approximately 20%, or even between approximately 0.1% and approximately 15% by weight relative to the total weight of the composition.
- 6Composition according to the preceding claim, characterized by the fact that the content of composite pigment in the composition is between approximately 0.3% and approximately 10% by weight relative to the total weight of the composition.
- 7Composition according to the preceding claim, characterized by the fact that the content of composite pigment in the composition is between 1% and 5% by weight relative to the total weight of the composition.
- 8Composition according to any one of the preceding claims, characterized by the fact that the organic coloring matter comprises at least one organic pigment.
- 9Composition according to any one of the preceding claims, characterized by the fact that the organic coloring matter comprises at least one organic lacquer.
- 10Composition according to any one of the preceding claims, characterized by the fact that the inorganic nucleus has an average size of between approximately 1 nm and approximately 100 nm.
- 11Composition according to the preceding claim, characterized by the fact that the inorganic nucleus has an average size of between approximately 5 nm and approximately 75 nm.
- 13Composition according to any one of the preceding claims, characterized by the fact that the inorganic nucleus has a refractive index greater than or equal to 2.
- 14Composition according to the preceding claim, characterized by the fact that the refractive index of the inorganic nucleus is greater than or equal to 2.1.
- 15Composition according to the preceding claim, characterized by the fact that the refractive index of the inorganic nucleus is greater than or equal to 2.2.
- 16Composition according to any one of the preceding claims, characterized by the fact that the inorganic nucleus has a specific surface of between approximately 1 m 2 / g and about 1000 m 2 / g.
- 17Composition according to the preceding claim, characterized by the fact that the specific surface of the inorganic nucleus is between approximately 10 m 2 / g and about 600 m 2 / g.
- 19Composition according to any one of the preceding claims, characterized by the fact that the inorganic nucleus comprises a material chosen from a metal salt, a metal oxide, an alumina, a glass, a ceramic, a graphite, a silica, a silicate, a synthetic mica, and one of their mixtures.
- 20Composition according to the preceding claim, characterized by the fact that the inorganic nucleus comprises a metal oxide chosen from an oxide of titanium, zirconium, cerium, zinc, iron, ferric blue, chromium and aluminum.
- 22Composition according to the preceding claim, characterized by the fact that the inorganic nucleus contains titanium dioxide.
- 23Composition according to Claim 19, characterized by the fact that the inorganic nucleus comprises at least one silicate chosen from an aluminosilicate and a borosilicate.
- 24Composition according to Claim 19, characterized by the fact that the inorganic nucleus contains silica.
- 25Composition according to any one of the preceding claims, characterized by the fact that the mass proportion of the organic coloring matter is between approximately 10 and approximately 500 parts by weight per 100 parts by weight of the inorganic nucleus.
- 26Composition according to the preceding claim, characterized by the fact that the mass proportion of the organic coloring matter is between approximately 20 and approximately 250 parts by weight per 100 parts by weight of the inorganic nucleus.
- 27Composition according to the preceding claim, characterized by the fact that the mass proportion of the organic coloring matter is between approximately 40 and approximately 125 parts by weight per 100 parts by weight of the inorganic nucleus.
- 28Composition according to any one of the preceding claims, characterized by the fact that the organic coloring matter is chosen from a cochineal carmine, an organic pigment of azo dye, anthraquinone, indigo, xanthene, pyrenic, quinolinic, triphenylmethane, fluoran, an organic lacquer or an insoluble salt of sodium, potassium, calcium , barium, aluminum, zirconium, strontium, titanium, acid dye.
- 29Composition according to the preceding claim, characterized by the fact that the acid dye is chosen from an azo, anthraquinonic, indigo, xanthene, pyrenic, quinolinic, triphenylmethane, fluorane dye and any other dye comprising at least one carboxylic or sulfonic acid group.
- 30Composition according to any one of the preceding claims, characterized by the fact that the organic coloring matter comprises an organic lacquer which is supported by an organic support comprising at least one rosin or aluminum benzoate.
- 31Composition according to any one of the preceding claims, characterized by the fact that the organic coloring matter comprises an organic pigment having one of the following names:D&C Blue n ° 4, D&C Brown n ° 1, D&C Green n ° 5, D&C Green n ° 6, D&C Orange n ° 4, D&C Orange n ° 5, D&C Orange n ° 10, D&C Orange n ° 11, D&C Red n ° 6, D&C Red n ° 7, D&C Red n ° 17, D&C Red n ° 21, D&C Red n ° 22, D&C Red n ° 27, D&C Red n ° 28, D&C Red n ° 30, D&C Red n ° 31, D&C Red n ° 33, D&C Red n ° 34, D&C Red n ° 36, D&C Violet n ° 2, D&C Yellow n ° 7, D&C Yellow n ° 8, D&C Yellow n ° 10, D&C Yellow n ° 11, FD&C Blue n ° 1, FD&C Green n ° 3, FD&C Red n ° 40, FD&C Yellow n ° 5, FD&C Yellow n ° 6.
- 32Composition according to any one of the preceding claims, characterized by the fact that the organic coloring matter comprises an organic lacquer having one of the following names:D&C Red n ° 2 Aluminum lake, D&C Red n ° 3 Aluminum lake, D&C Red n ° 4 Aluminum lake, D&C Red n ° 6 Aluminum lake, D&C Red n ° 6 Barium lake, D&C Red n ° 6 Barium / Strontium lake, D&C Red n ° 6 Strontium lake, D&C Red n ° 6 Potassium lake, D&C Red n ° 7 Aluminum lake, D&C Red n ° 7 Barium lake, D&C Red n ° 7 Calcium lake, D&C Red n ° 7 Calcium / Strontium lake, D&C Red n ° 7 Zirconium lake, D&C Red n ° 8 Sodium lake, D&C Red n ° 9 Aluminum lake, D&C Red n ° 9 Barium lake, D&C Red n ° 9 Barium / Strontium lake, D&C Red n ° 9 Zirconium lake, D&C Red n ° 10 Sodium lake, D&C Red n ° 19 Aluminum lake, D&C Red n ° 19 Barium lake, D&C Red n ° 19 Zirconium lake, D&C Red n ° 21 Aluminum lake, D&C Red n ° 21 Zirconium lake, D&C Red n ° 22 Aluminum lake, D&C Red n ° 27 Aluminum lake, D&C Red n ° 27 Aluminum / Titanium / Zirconium lake, D&C Red n ° 27 Barium lake, D&C Red n ° 27 Calcium lake, D&C Red n ° 27 Zirconium lake, D&C Red n ° 28 Aluminum lake, D&C Red n ° 30 lake, D&C Red n ° 31 Calcium lake, D&C Red n ° 33 Aluminum lake, D&C Red n ° 34 Calcium lake, D&C Red n ° 36 lake, D&C Red n ° 40 Aluminum lake, D&C Blue n ° 1 Aluminum lake, D&C Green n ° 3 Aluminum lake, D&C Orange n ° 4 Aluminum lake, D&C Orange n ° 5 Aluminum lake, D&C Orange n ° 5 Zirconium lake, D&C Orange n ° 10 Aluminum lake, D&C Orange n ° 17 Barium lake, D&C Yellow n ° 5 Aluminum lake, D&C Yellow n ° 5 Zirconium lake, D&C Yellow n ° 6 Aluminum lake, D&C Yellow n ° 7 Zirconium lake, D&C Yellow n ° 10 Aluminum lake, FD&C Blue n ° 1 Aluminum lake, FD&C Red n ° 4 Aluminum lake, FD&C Red n ° 40 Aluminum lake, FD&C Yellow n ° 5 Aluminum lake, FD&C Yellow n ° 6 Aluminum lake.
- 33Composition according to any one of the preceding claims, characterized by the fact that said at least one composite pigment comprises at least one binder contributing to the fixing of the organic coloring matter on the inorganic nucleus.
- 34Composition according to Claim 33, characterized by the fact that the binder is organic.
- 36Composition according to the preceding claim, characterized by the fact that the coupling agent is based on silane, titanate, aluminate, and / or zirconate, or a mixture of these.
- 37Composition according to Claim 35, characterized by the fact that the binder comprises at least one silicone compound.
- 39Composition according to any one of the preceding claims, characterized by the fact that it is free of uncoated titanium dioxide particles.
- 40Composition according to any one of the preceding claims, characterized by the fact that it comes in a solid form.
- 41Composition according to any one of the preceding claims, characterized by the fact that it is in liquid, pasty or gelled form.
- 42Composition according to any one of the preceding claims, characterized by the fact that the composite pigment is different from an interference pigment.
- 43Composition according to any one of the preceding claims, characterized by the fact that the saturation C * of the composite pigment is greater than or equal to 30.
- 44Composition according to any one of the preceding claims, characterized by the fact that organic coloring matter is different from melanin.
- 45Composition according to any one of the preceding claims, characterized by the fact that the total content of organic coloring matter in the composition is less than or equal to 10% by weight.
Independent claims44
176 paragraphs, as filed
0001The present invention relates to cosmetic compositions intended to be applied to the skin, including the mucous membranes, in particular the lips, and the integuments, in particular the nails, eyelashes, eyebrows and hair.
0002Organic coloring matters are commonly used to bring color to cosmetic compositions. However, conventional organic coloring materials do not make it possible to obtain compositions having a satisfactory covering power. In addition, the colors provided by these organic coloring materials vary greatly between the dry state and the state in dispersion in a cosmetic solvent.
0003There is a need to have cosmetic compositions having a satisfactory saturation C * and a sufficiently high covering power.
0004There is still a need for pigments having a slight change in color depending on the surrounding environment.
0005The present invention aims to meet all or part of the aforementioned needs.
0006It achieves this by virtue of a composition having a covering power advantageously between approximately 25 and approximately 100, for example between approximately 25 and approximately 90, or even between approximately 30 and approximately 100, for example between 30 and approximately 90, this composition being intended to be applied to the skin, the lips and / or the integuments and comprising particles of at least one composite pigment, these particles comprising:<ul id="ul0001" list-style="dash" compact="compact"><li>an inorganic nucleus,</li><li>at least one at least partial coating of at least one organic coloring matter in an amount sufficient for the saturation C * of the composition to be preferably between approximately 25 and approximately 100, or even between approximately 30 and approximately 100.</li></ul>
0007Thanks to the invention, it is possible to obtain compositions which are both saturated and covering.
0008The content of composite pigment in the composition may be between approximately 0.1% and approximately 30%, or even between approximately 0.1% and approximately 20%, for example between approximately 0.1% and approximately 15%, or even between approximately 0.3% and 10% approximately, for example between approximately 1% and approximately 5% by weight, relative to the total weight of the composition.
0009In particular, it is possible to choose a relatively high composite pigment content in order to obtain the desired covering power and in particular a relatively high covering power.
0010A suitable shade can be obtained in various ways, for example by mixing the composite pigments according to the invention, these pigments having different colors and / or by the presence of several organic coloring matters in the coating of the cores of the pigment (s). composites, these organic coloring matters being, for example, mixed or present in respective layers of the coating.
0011By "an at least partial coating" is meant within the meaning of the present invention, a coating of all or part of the inorganic nucleus.
0012The composition according to the invention can comprise a physiologically acceptable medium.
0013By "physiologically acceptable medium" is meant a non-toxic medium capable of being applied to the skin, the lips or the integuments of human beings, in particular a cosmetic medium. The physiologically acceptable medium will be adapted to the nature of the support on which the composition is to be applied, as well as to the form in which the composition is intended to be packaged, in particular solid or fluid at room temperature and under atmospheric pressure.
0014By "cosmetic composition" is meant a composition as defined in Council Directive 93/35 / EEC of June 14, 1993.
<i><b>MEASUREMENT OF SATURATION C *</b></i>
0015In the case of a liquid or pasty composition, a sample of the composition to be studied is introduced into a metal dish about 1 cm deep. A 1 mm thick quartz slide is applied to the composition, taking care to avoid air bubbles before making the measurement.
0016In the case of a powder composition, the powder sample is compacted at a pressure of 10 MPa in a metal cup about 1 cm deep. A 1 mm thick quartz slide is applied to the composition before making the measurement.
0017In the case of a stick, the composition is poured into a flat bottom quartz mold about 2 cm deep.
0018The trichromatic coordinates L *, a *, b * of the composition in the CIE space L * a * b * are measured using a CM-508d spectrocolorimeter from MINOLTA, under illuminant D65, with a specular component included and a d / 8 lighting system.
0019The saturation C * of the composition is calculated using the formula C * = [(a *)<sup>2</sup>+ (b *)<sup>2</sup>]<sup>1/2</sup>.
<i><b>MEASUREMENT OF COVERING POWER</b></i>
0020In the case of a stick, the formulation is previously kneaded so as to obtain a viscous paste.
0021In the case of a powder, 50 parts by weight of the powder are mixed with 50 parts by weight of dimethicone (DC 200 Fluid 5CST from DOW CORNING) so as to obtain a viscous paste.
0022The formulation is then spread with a thickness of 30 μm on an Erichsen contrast card, type 24/5, having a black background and a white background, and the trichromatic coordinates (X, Y, Z) are measured using '' a CR-300 colorimeter.
0023Similar spreads are made on two other contrast cards and three measurements are made on each card. The average corresponding to these nine measurements is then calculated.
0024The covering power is equal to 100 x Yn / Yb where Yn is the average value of Y on a black background and Yb is the average value of Y on a white background. A covering power of 100 corresponds to a completely opaque formulation.
<i><b>COMPOSITE PIGMENT</b></i>
<i><b>Structure</b></i>
0025A composite pigment according to the invention can be composed in particular of particles comprising:<ul id="ul0002" list-style="dash" compact="compact"><li>an inorganic nucleus,</li><li>at least one at least partial coating of at least one organic coloring matter.</li></ul>
0026At least one binder can advantageously contribute to the fixation of the organic coloring matter on the inorganic nucleus.
0027The composite pigment particles can have various shapes. These particles may in particular be in the form of platelets or globular, in particular spherical, and may be hollow or solid. By "in the form of platelets" is meant particles whose ratio of the largest dimension to the thickness is greater than or equal to 5.
0028A composite pigment according to the invention may for example have a specific surface of between 1 and 1000 m 2<sup>2</sup>/ g, especially between 10 and 600 m<sup>2</sup>/ g approximately, and in particular between 20 and 400 m<sup>2</sup>/ g approximately. The specific surface is the value measured by the BET method.
0029The mass proportion of the core can exceed 50% relative to the total weight of the composite pigment, for example ranging from 50% to 70%, for example from 60% to 70%.
0030The composition may comprise only one or more composite pigments as defined above or alternatively comprise one or more composite pigments other as well as pigments having a non-composite structure, in particular mineral, interference pigments, lakes or organic pigments. The composition can in particular be devoid of TiO particles<sub>2</sub> uncoated.
0031The composite pigment may be different from an interference pigment as described for example in US Pat. No. 6,428,773. An interference pigment comprises, for example, several layers of constant thicknesses of materials selected to be able to produce optical interference.
0032The saturation C * of the composite pigment can be greater than or equal to 30, measured according to the protocol below.
<b>Composite pigment saturation measurement protocol</b>
:
0033The a * and b * values in the CIE L * a * b * space of the composite pigment are measured as follows:
0034The pure composite pigment is compacted in a rectangular cup having the dimensions 2 x 1.5 cm and a depth of 3 mm, by applying a pressure of 100 bars.
0035The a * and b * values of the compacted pigment are measured with a MINOLTA 3700d spectrophotometer, in specular mode excluded, under illuminant D65, medium aperture. Saturation is given by C * = (a *<sup>2</sup> + b *<sup>2</sup>)<sup>1/2</sup>.
<i><b>Inorganic core</b></i>
0036The inorganic nucleus can be of any shape suitable for fixing particles of organic coloring matter, for example spherical, globular, granular, polyhedral, acicular, fusiform, flattened in the form of a flake, rice grain, tortoiseshell, as well as 'a combination of these forms, this list not being exhaustive.
0037Preferably, the ratio of the largest dimension of the core to its smallest dimension is between 1 and 50.
0038The inorganic nucleus may have an average size of between approximately 1 nm and approximately 100 nm, or even between approximately 5 nm and approximately 75 nm, for example between approximately 10 nm and approximately 50 nm, in particular 20 or 25 nm.
0039By "average size" is meant the dimension given by the statistical particle size distribution to half the population, called D50. The average size can be a number average size determined by image analysis (electron microscopy).
0040The inorganic nucleus may have a refractive index greater than or equal to 2, or even greater than or equal to 2.1, for example greater than or equal to 2.2.
0041The inorganic nucleus can be produced from a material chosen from the non-limiting list comprising the metal salts and metal oxides, in particular the oxides of titanium, zirconium, cerium, zinc, iron, ferric blue, aluminum and chromium, aluminas, glasses, ceramics, graphite, silicas, silicates, in particular aluminosilicates and borosilicates, synthetic mica, and mixtures thereof.
0042Titanium oxides, especially TiO<sub>2</sub>, iron, especially Fe<sub>2</sub>O<sub>3</sub>, cerium, zinc and aluminum, silicates, especially aluminosilicates and borosilicates are particularly suitable.
0043The inorganic nucleus may have a specific surface, measured by the BET method, for example between approximately 1 m<sup>2</sup>/ g and about 1000 m<sup>2</sup>/ g, better between about 10 m<sup>2</sup>/ g and about 600 m<sup>2</sup>/ g, for example between about 20 m<sup>2</sup>/ g and about 400 m<sup>2</sup>/ g.
0044The inorganic nucleus can be colored, if desired.
<i><b>Organic coloring matter</b></i>
0045The organic coloring matter may for example comprise at least one organic pigment, for example at least one organic lacquer.
0046The organic coloring matter can be chosen, for example, from particulate compounds which are insoluble in the physiologically acceptable medium of the composition.
0047The organic coloring matter can comprise, for example pigments, for example organic lakes or other organic coloring matters, which can be chosen from the compounds below and their mixtures:<ul id="ul0003" list-style="dash" compact="compact"><li>cochineal carmine,</li><li>organic pigments of azo, anthraquinone, indigo, xanthenic, pyrenic, quinolinic, triphenylmethane, fluorane dyes,</li><li>organic lakes or insoluble salts of sodium, potassium, calcium, barium, aluminum, zirconium, strontium, titanium, acid dyes such as azo dyes, anthraquinones, indigoids, xanthenics, pyrenics, quinolines, triphenylmethane, fluorane, these dyes may contain at least one carboxylic or sulfonic acid group.</li></ul>
0048Among the organic pigments, mention may in particular be made of those known under the following names: D&C Blue n ° 4, D&C Brown n ° 1, D&C Green n ° 5, D&C Green n ° 6, D&C Orange n ° 4, D&C Orange n ° 5, D&C Orange n ° 10, D&C Orange n ° 11, D&C Red n ° 6, D&C Red n ° 7, D&C Red n ° 17, D&C Red n ° 21, D&C Red n ° 22, D&C Red n ° 27, D&C Red n ° 28, D&C Red n ° 30, D&C Red n ° 31, D&C Red n ° 33, D&C Red n ° 34, D&C Red n ° 36, D&C Violet n ° 2, D&C Yellow n ° 7, D&C Yellow n ° 8, D&C Yellow n ° 10, D&C Yellow n ° 11, FD&C Blue n ° 1, FD&C Green n ° 3, FD&C Red n ° 40, FD&C Yellow n ° 5, FD&C Yellow n ° 6.
0049The organic coloring matter can comprise an organic lacquer supported by an organic support such as rosin or aluminum benzoate, for example.
0050Among the organic lacquers, mention may in particular be made of those known under the following names: D&C Red n ° 2 Aluminum lake, D&C Red n ° 3 Aluminum lake, D&C Red n ° 4 Aluminum lake, D&C Red n ° 6 Aluminum lake, D&C Red n ° 6 Barium lake, D&C Red n ° 6 Barium / Strontium lake, D&C Red n ° 6 Strontium lake, D&C Red n ° 6 Potassium lake, D&C Red n ° 7 Aluminum lake, D&C Red n ° 7 Barium lake, D&C Red n ° 7 Calcium lake, D&C Red n ° 7 Calcium / Strontium lake, D&C Red n ° 7 Zirconium lake, D&C Red n ° 8 Sodium lake, D&C Red n ° 9 Aluminum lake, D&C Red n ° 9 Barium lake, D&C Red n ° 9 Barium / Strontium lake, D&C Red n ° 9 Zirconium lake, D&C Red n ° 10 Sodium lake, D&C Red n ° 19 Aluminum lake, D&C Red n ° 19 Barium lake, D&C Red n ° 19 Zirconium lake, D&C Red n ° 21 Aluminum lake, D&C Red n ° 21 Zirconium lake, D&C Red n ° 22 Aluminum lake, D&C Red n ° 27 Aluminum lake, D&C Red n ° 27 Aluminum / Titanium / Zirconium lake, D&C Red n ° 27 Barium lake, D&C Red n ° 27 Calcium lake, D&C Red n ° 27 Zirconium lake, D&C Red n ° 28 Aluminum lake, D&C Red n ° 30 lake, D&C Red n ° 31 Calcium lake, D&C Red n ° 33 Aluminum lake, D&C Red n ° 34 Calcium lake, D&C Red n ° 36 lake, D&C Red n ° 40 Aluminum lake, D&C Blue n ° 1 Aluminum lake, D&C Green n ° 3 Aluminum lake, D&C Orange n ° 4 Aluminum lake, D&C Orange n ° 5 Aluminum lake, D&C Orange n ° 5 Zirconium lake, D&C Orange n ° 10 Aluminum lake, D&C Orange n ° 17 Barium lake, D&C Yellow n ° 5 Aluminum lake, D&C Yellow n ° 5 Zirconium lake, D&C Yellow n ° 6 Aluminum lake, D&C Yellow n ° 7 Zirconium lake, D&C Yellow n ° 10 Aluminum lake, FD&C Blue n ° 1 Aluminum lake, FD&C Red n ° 4 Aluminum lake, FD&C Red n ° 40 Aluminum lake, FD&C Yellow n ° 5 Aluminum lake, FD&C Yellow n ° 6 Aluminum lake.
0051The chemical compounds corresponding to each of the organic coloring matters mentioned above are mentioned in the book “International Cosmetic Ingredient Dictionnary and Handbook”, Edition 1997, pages 371 to 386 and 524 to 528, published by “The Cosmetic, Toiletry, and Fragrance Association ”, The content of which is incorporated into this application by reference.
0052The mass proportion of organic coloring matter can be between approximately 10 parts and approximately 500 parts by weight per 100 parts of the inorganic nucleus, or even between approximately 20 parts and approximately 250 parts by weight, for example between approximately 40 parts and approximately 125 parts in weight per 100 parts of the inorganic nucleus.
0053The total content of organic coloring matter in the composition, originating from the composite pigment and from other optional pigments, may for example be less than 10%, relative to the total weight of the composition.
0054The proportion of the organic coloring matter may exceed 30% relative to the total weight of the composite pigment, for example ranging from 30 to 50%, for example from 30 to 40%.
<i><b>Binder</b></i>
0055The binder can be of any type as long as it allows the organic coloring matter to adhere to the surface of the inorganic core.
0056The binder can in particular be chosen from a non-limiting list comprising silicone compounds, polymeric, oligomeric or similar compounds, and in particular from organosilanes, fluoroalkylated organosilanes and polysiloxanes, for example polymethylhydrogenosiloxane, as well as various coupling agents, such as coupling agents based on silanes, titanates, aluminates, zirconates and their mixtures.
0057The silicone compound can be chosen from a non-limiting list comprising in particular:<ul id="ul0004" list-style="dash" compact="compact"><li>organosilanes (1) obtained from alkoxysilanes,</li><li>the polysiloxanes (2) modified or not chosen from a non-limiting list comprising:<ul id="ul0005" list-style="dash" compact="compact"><li>modified polysiloxanes (2A) comprising at least one radical chosen from, in particular, polyethers, polyesters and epoxy compounds (they will be called “modified polysiloxanes”),</li><li>polysiloxanes (2B) relating to a silicon atom located at the end of the polymer, at least one group chosen from a non-limiting list comprising carboxylic acids, alcohols or hydroxy groups, and</li><li>fluoroalkylated organosilane compounds (3) obtained from fluoroalkylsilanes.</li></ul></li></ul>
0058The organosilane compounds (1) can be obtained from alkoxysilane compounds represented by formula (I): R<sup>1</sup> <sub>at</sub> If X<sub>4-a</sub> (I) in which :<ul id="ul0006" list-style="dash" compact="compact"><li>R<sup>1</sup> represents C<sub>6</sub>H<sub>5</sub>-, (CH<sub>3</sub>)<sub>2</sub> CH-CH<sub>2</sub>- or a type C radical<sub>b</sub> H<sub>2b + 1</sub>- (where b varies from 1 to 18),</li><li>X represents CH<sub>3</sub>O- or C<sub>2</sub>H<sub>5</sub>O-, and</li><li>a ranges from 0 to 3.</li></ul>
0059Specific examples of alkoxysilane compounds can include the alkoxysilanes selected from: methyltriethoxysilane, dimethyldiethoxysilane, phenyltriethoxysilane, diphenyldiethoxysilane, methyltrimethoxysilane, dimethyldimethoxysilane, phenyltrimethoxysilane, diphenyldimethoxysilane, isobutyltrimethoxysilane, decyltrimethoxysilane and the like, in particular from methyltriethoxysilane, phenyltriethoxysilane, methyltrimethoxysilane, dimethyldimethoxysilane, the isobutyltrimethoxysilane, and even better methyltriethoxysilane, methyltrimethoxysilane, phenyltriethoxysilane.
0060The polysiloxanes (2) can in particular correspond to formula (II):<chemistry id="chem0001" num="0001"><img file="EP1586296A1_D0001.tif" /></chemistry> in which R<sup>2</sup> represents H- or CH<sub>3</sub>- and d varies from 15 to 450.
0061Among these polysiloxanes, those for which R<sup>2</sup> represents H are preferred.
0062The modified polysiloxanes (2A) can in particular respond to the following formulas:<ul id="ul0007" list-style="dash" compact="compact"><li>(at<sup>1</sup>) modified polysiloxanes carrying polyethers, represented by formula (III)<chemistry id="chem0002" num="0002"><img file="EP1586296A1_D0002.tif" /></chemistry></li></ul> in which R<sup>3</sup> represents - (CH<sub>2</sub>)<sub>h</sub>-; R<sup>4</sup> represents - (CH<sub>2</sub>)<sub>i</sub>- CH<sub>3</sub> ; R<sup>5</sup> represents -OH, - COOH, -CH = CH<sub>2</sub>, -C (CH<sub>3</sub>) = CH<sub>2</sub> or - (CH<sub>2</sub>)<sub>j</sub>- CH<sub>3</sub> ; R<sup>6</sup> represents - (CH2)<sub>k</sub>- CH<sub>3</sub> ; g and h independently varying from 1 to 15; j and k independently varying from 0 to 15; e varying from 1 to 50 and f varying from 1 to 300,<ul id="ul0008" list-style="dash" compact="compact"><li>(at<sup>2</sup>) modified polysiloxanes carrying polyesters, represented by formula (IV):<chemistry id="chem0003" num="0003"><img file="EP1586296A1_D0003.tif" /></chemistry> in which R<sup>7</sup>, R<sup>8</sup> and R<sup>9</sup> independently represent - (CH<sub>2</sub>)<sub>q</sub>-; R<sup>10</sup> represents -OH; -COOH, -CH = CH<sub>2</sub>, -C (CH<sub>3</sub>) = CH<sub>2</sub> or - (CH<sub>2</sub>)<sub>r</sub>- CH<sub>3</sub> ; R<sup>11</sup> represents - (CH<sub>2</sub>)<sub>s</sub>- CH<sub>3</sub> ; n and q independently varying from 1 to 15, r and s independently varying from 0 to 15; e varying from 1 to 50 and f varying from 1 to 300,</li><li>(at<sup>3</sup>) modified polysiloxanes carrying epoxy radicals represented by formula (V):<chemistry id="chem0004" num="0004"><img file="EP1586296A1_D0004.tif" /></chemistry></li></ul> in which R<sup>12</sup> represents - (CH<sub>2</sub>)<sub>v</sub>-; v varying from 1 to 15; t varying from 1 to 50 and u varying from 1 to 300; or their mixtures. Among the modified polysiloxanes (2A), the modified polysiloxanes carrying polyethers of formula (III) are preferred. The polysiloxanes modified on the terminal part (2B) can correspond to the formula (VI):<chemistry id="chem0005" num="0005"><img file="EP1586296A1_D0005.tif" /></chemistry> in which R<sup>13</sup> and R<sup>14</sup> can represent -OH, R<sup>16</sup>-OH or R<sup>17</sup>-COOH, independently of each other; R<sup>15</sup> represents -CH<sub>3</sub> or -C<sub>6</sub>H<sub>5</sub> ; R<sup>16</sup> and R<sup>17</sup> represent - (CH<sub>2</sub>)<sub>y</sub>-; y varying from 1 to 15; w varying from 1 to 200 and x varying from 0 to 100.
0063Among these polysiloxanes modified on at least one end, those carrying at least radical (R<sup>16</sup> and / or R<sup>17</sup>) carrying a carboxylic acid group on at least one terminal silicon atom are more preferred.
0064The fluoroalkylated organosilane compounds (3) can be obtained from fluoroalkyl silanes represented by the formula (VII): CF<sub>3</sub>(CF<sub>2</sub>)<sub>z</sub>CH<sub>2</sub>CH<sub>2</sub> (R<sup>18</sup>)<sub>at</sub> Six<sub>4-a</sub> (VII) in which :<ul id="ul0009" list-style="dash" compact="compact"><li>R<sup>18</sup> represents CH<sub>3</sub>-, VS<sub>2</sub>H<sub>5</sub>-, CH<sub>3</sub>O- or C<sub>2</sub>H<sub>5</sub>O-,</li><li>X represents CH<sub>3</sub>O- or C<sub>2</sub>H<sub>5</sub>O-,</li><li>Z ranges from 0 to 15 and a ranges from 0 to 3.</li></ul>
0065The fluoroalkylsilanes may be selected in a non limiting list trifluoropropyltrimethoxysilane, tridecafluorooctyltrimethoxysilane, heptadecafluorodecyltrimethoxysilane, the heptadécafluorodécylméthyldiméthoxysilane, trifluoropropyltriethoxysilane, tridecafluorooctyltriethoxysilane, heptadecafluorodecyltriethoxysilane, heptadecafluorodecylmethyldiethoxysilane and the like, in particular trifluoropropyltrimethoxysilane, tridecafluorooctyltrimethoxysilane and heptadecafluorodecyltrimethoxysilane, and even better trifluoropropyl trimethoxysilane and tridecafluorooctyltrimethoxysilane.
0066The silane-based coupling agents can be chosen from a non-limiting list comprising in particular vinyltrimethoxysilane, vinyltriethoxysilane, γ-aminopropyl-triethoxysilane, γ-flycidoxypropyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, γ-methacroxy, γ-methacroxy ) -γ-aminopropyltrimethoxysilane, γ-glycidoxypropylmethyldimethoxysilane, γ-chloropropyltrimethoxysilane and the like.
0067Titanate-based coupling agents can be chosen from the list comprising isopropylstearoyl titanate, isopropyltris (dioctylpyrophosphate) titanate, isopropyltri (N-aminoethylaminoethyl) titanate, tetraoctylbis (ditridecylphosphate) titanate tetra (2,2-diaryloxymethyl-1-butyl) bis (ditridecyl) phosphate, bis (dioctylpyrophosphate) oxyacetate titanate, bis (dioctylpyrophosphate) ethylene titanate and the like.
0068The aluminate-based coupling agents can be chosen from acetoalkoxyaluminum diisopropylate, aluminum diisopropoxymonoethylacetoacetate, aluminum triethylacetoacetate, aluminum triacetylacetonate and the like.
0069The zirconate-based coupling agents can be chosen from a list comprising in particular zirconium tetrakisacetylacetonate, zirconium dibutoxybisacetylacetonate, zirconium tetrakisethylacetoacetate, tributoxymonoethylacetoacetate of zirconium, their tributoxyacetylacetonate.
0070The compounds serving as a binder can in particular have a molar mass which can vary between 300 and 100,000.
0071To obtain a layer covering the inorganic cores uniformly, the binder is preferably in a liquid state or soluble in water or in different solvents.
0072The amount of binder can vary from 0.01 to 15%, in particular from 0.02 to 12.5% and in particular from 0.03 to 10% by weight (calculated relative to C or Si) relative to the weight of the particles comprising the nucleus and the binder. For further details on how to calculate the relative quantity of the binder, reference may be made to application EP 1 184 426 A2. The relative proportion of binder can be less than or equal to 5%, for example less than or equal to 3%, relative to the total weight of the composite pigment.
<i><b>Preparation of the composite pigment</b></i>
0073The composite pigment can be prepared by any suitable method, for example a mechanical-chemical method or a method of precipitation in solution, with dissolution of the organic coloring matter then precipitation on the surface of the core.
0074A binder may or may not be used.
0075A method comprising a mechanical mixing of an organic pigment and the inorganic nucleus is preferred.
0076A binder can be added and mixed with the inorganic core before the introduction of the organic coloring matter.
0077The composite pigment can be produced, for example, by one of the methods described in European patent applications EP 1 184 426 and EP 1 217 046, the contents of which are incorporated here by reference, advantageously by the method described in application EP 1 184,426.
0078In an example of implementation, one begins by mixing the particles intended to constitute the inorganic nucleus with the binder.
0079In order for the binder to adhere uniformly to the surface of the inorganic core, it is preferable to pass these particles beforehand through a grinder, so as to deagglomerate them.
0080The mixing and stirring conditions are chosen so that the core is uniformly covered with binder. These conditions can be controlled so that the linear load is between 19.6 and 19,160 N / cm, in particular between 98 and 14,170 N / cm and better still between 147 and 980 N / cm; the treatment time is in particular between 5 min and 24 hours and better still from 10 min to 20 hours; the rotation speed can be between 2 and 1000 rpm, in particular between 5 and 1000 rpm and better still between 10 and 800 rpm.
0081After the binder has covered the inorganic core, the organic coloring matter is added and mixed with agitation to adhere to the binder layer.
0082The addition methods can be, for example, addition by large quantity, continuously, or by small quantity.
0083Mixing and stirring, whether of inorganic nuclei with the binder or of organic coloring matter with the inorganic nuclei covered with binder, can be carried out using an apparatus capable of applying a spatial cutting and / or compressive force to the mixture powders. Such devices are, for example, wheel, blade and similar mixers. Wheeled mixers are particularly suitable. A list of suitable devices is given in application EP 1 184 426 A2.
0084Another method of manufacturing a composite pigment is described in patent JP 3286463, which discloses a method of precipitation in solution.
0085The organic coloring matter is dissolved in ethanol, the inorganic nuclei are then dispersed in this ethanolic solution.
0086Then, an alkaline aqueous solution of sodium or potassium carbonate is slowly added to these mixtures, then last, slowly, an ethanolic solution of calcium chloride, all with stirring.
<i><b>OTHER COMPONENTS</b></i>
<i><b>Solvents</b></i>
0087The composition can comprise at least one aqueous or organic solvent.
0088When the composition comprises one or more organic solvents, these solvents may be present in a content ranging from 0.1% to 99%, relative to the total weight of the composition.
0089Generally, the amount of solvent (s), in particular organic (s), will depend on the nature of the support on which the composition is intended to be applied.
0090In the case of a nail varnish, for example, the organic solvent may be present in the composition at a content ranging for example from 30 to 99% by weight and preferably from 60% to 90% by weight, relative to the total weight of the composition.
0091The composition can comprise at least one organic solvent chosen from the following list:<ul id="ul0010" list-style="dash" compact="compact"><li>ketones that are liquid at room temperature, such as methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, isophorone, cyclohexanone, acetone;</li><li>alcohols liquid at room temperature such as ethanol, isopropanol, diacetone alcohol, 2-butoxyethanol, cyclohexanol;</li><li>glycols which are liquid at room temperature such as ethylene glycol, propylene glycol, pentylene glycol, glycerol;</li><li>propylene glycol ethers which are liquid at room temperature such as propylene glycol monomethyl ether, propylene glycol monomethyl ether acetate, dipropylene glycol mono n-butyl ether;</li><li>short chain esters (having 3 to 8 carbon atoms in total) such as ethyl acetate, methyl acetate, propyl acetate, n-butyl acetate, acetate d 'isopentyle;</li><li>alkanes which are liquid at room temperature such as decane, heptane, dodecane, cyclohexane;</li></ul>
0092The composition can also comprise water or a mixture of water and hydrophilic organic solvents commonly used in cosmetics such as alcohols and in particular linear or branched lower monoalcohols having from 2 to 5 carbon atoms such as ethanol, isopropanol or n-propanol, polyols such as glycerin, diglycerin, propylene glycol, sorbitol, pentethylene glycol, polyethylene glycols. The composition may, in addition, contain C ethers<sub>2</sub> and C aldehydes<sub>2</sub>-VS<sub>4</sub> hydrophilic. The water or the mixture of water and hydrophilic organic solvents may be present in the composition in a content ranging for example from 0% to 90%, in particular 0.1% to 90% by weight and preferably from 0% to 60% by weight, in particular 0.1% to 60% by weight, relative to the total weight of the composition.
<i><b>Fat phase</b></i>
0093The composition, in particular when it is intended to be applied to the lips, can comprise an oily phase and in particular at least one fatty substance liquid at room temperature (25 ° C.) and / or a fatty substance solid at room temperature such as waxes, pasty fatty substances, gums, and mixtures thereof. The fatty phase may, in addition, contain lipophilic organic solvents.
0094The composition may for example have a continuous fatty phase, which may contain less than 5% of water, in particular less than 1% of water relative to its total weight and in particular be in anhydrous form.
0095As fatty substances liquid at room temperature, often called "oils", there may be mentioned: vegetable hydrocarbon oils such as liquid triglycerides of fatty acids of 4 to 10 carbon atoms such as triglycerides of heptanoic or octanoic acids, or even sunflower, corn, soybean, grape seed, sesame oils, apricot, macadamia, castor, avocado, caprylic / capric acid triglycerides, jojoba oil, shea butter, lanolin, acetylated lanolin; linear or branched hydrocarbons, of mineral or synthetic origin such as paraffin oils and their derivatives, petrolatum, polydecenes, hydrogenated polyisobutene such as parlameam; synthetic esters and ethers, in particular of fatty acids such as, for example, Purcellin oil, isopropyl myristate, ethyl-2-hexyl palmitate, octyl-2-dodecyl stearate, erucate octyl-2-dodecyl, isostearyl isostearate; hydroxylated esters such as isostearyl lactate, octylhydroxystearate, octyldodecyl hydroxystearate, diisostearylmalate, triisoketyl citrate, heptanoates, octanoates, decanoates of fatty alcohols; isononyl isonanoate, isopropyl lanolate, tridecyl trimellilate, diisostearyl malate; polyol esters such as propylene glycol dioctanoate, neopentylglycol diheptanoate, diethylene glycol diisononanoate; and pentaerythritol esters; fatty alcohols having from 12 to 26 carbon atoms such as octyldodecanol, 2-butyloctanol, 2-hexyldecanol, 2-undecylpentadecanol, oleic alcohol; partially hydrocarbon and / or silicone fluorinated oils; silicone oils such as polymethylsiloxanes (PDMS), volatile or not, linear or cyclic, liquid or pasty at room temperature such as cyclomethicones, dimethicones, optionally comprising a phenyl group, such as phenyl trimethicones, phenyltrimethylsiloxydiphenyl siloxanes, diphenylmethyldimethyl-trisilanes diphenyl dimethicones, phenyl dimethicones, polymethylphenyl siloxanes; their mixtures. The oils can be present in a content ranging from 0.01 to 90%, and better still from 0.1 to 85% by weight, relative to the total weight of the composition.
0096The pasty fatty substances are generally hydrocarbon compounds with a melting point between 25 and 60 ° C, preferably between 30 and 45 ° C, and / or a hardness between 0.001 and 0.5 MPa, preferably between 0.005 and 0.4 MPa, like lanolines and their derivatives.
0097Waxes can be solid at room temperature (25 ° C), reversible solid / liquid state change, having a melting temperature above 30 ° C up to 200 ° C, a hardness greater than 0.5 MPa, and exhibiting an anisotropic crystal organization in the solid state. In particular, the waxes can have a melting temperature above 25 ° C and better still above 45 ° C. The waxes can be hydrocarbon, fluorinated and / or silicone and be of vegetable, mineral, animal and / or synthetic origin. As usable waxes, mention may be made of beeswax, Carnauba or Candellila wax, paraffin, microcrystalline waxes, ceresin or ozokerite; synthetic waxes such as polyethylene or Fischer Tropsch waxes, silicone waxes such as alkyl or alkoxy-dimethicone having from 16 to 45 carbon atoms. The composition can contain from 0 to 50% by weight of waxes, relative to the total weight of the composition, or even from 1 to 30% by weight.
0098The gums which can be used are generally high molecular weight polydimethylsiloxanes (PDMS) or cellulose gums or polysaccharides.
<i><b>Film-forming polymer</b></i>
0099The composition may also comprise, for example, a film-forming polymer, in particular in the case of a mascara or a nail varnish. "Film-forming polymer" denotes a polymer capable of forming on its own or in the presence of an auxiliary film-forming agent, a continuous and adherent film on a support, in particular on keratin materials.
0100Among the film-forming polymers which can be used in a composition according to the invention, there may be mentioned inter alia synthetic polymers, of radical type or of polycondensate type, polymers of natural origin, such as nitrocellulose or cellulose esters, and their mixtures .
0101The film-forming polymers of the radical type may in particular be vinyl polymers or copolymers, in particular acrylic polymers.
0102The vinyl film-forming polymers can result from the polymerization of ethylenically unsaturated monomers having at least one acid group and / or esters of these acid monomers and / or amides of these acid monomers such as α, β-ethylenic unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, itaconic acid.
0103The vinyl film-forming polymers can also result from the homopolymerization or from the copolymerization of monomers chosen from vinyl esters such as vinyl acetate, vinyl neodecanoate, vinyl pivalate, vinyl benzoate and t-butyl benzoate. vinyl and styrene monomers such as styrene and alpha-methyl styrene.
0104Among the film-forming polycondensates, mention may be made of polyurethanes, polyesters, polyester amides, polyamides, and polyureas, this list not being limiting.
0105The polymers of natural origin, optionally modified, can be chosen from shellac resin, sandara gum, dammars, elemis, copals, cellulose polymers, such as nitrocellulose, ethylcellulose or the nitrocellulose esters chosen. , for example, among cellulose acetate, cellulose acetobutyrate, cellulose acetopropionate, and mixtures thereof.
0106The film-forming polymer can be present in the form of solid particles in aqueous or oily dispersion, generally known under the name of latex or pseudolatex. The film-forming polymer may comprise one or more stable dispersions of particles of generally spherical polymers of one or more polymers, in a physiologically acceptable liquid fatty phase. These dispersions are generally called NAD (Non-Aqueous Dispersion) of polymer as opposed to latexes which are aqueous dispersions of polymer. These dispersions can in particular be in the form of polymer nanoparticles in stable dispersion in said fatty phase. The nanoparticles are preferably of a size between 5 and 600 nm. The techniques for preparing these dispersions are well known to those skilled in the art.
0107As an aqueous dispersion of film-forming polymer, use may be made of the acrylic dispersions sold under the names NEOCRYL XK-90®, NEOCRYL A-1070®, NEOCRYL A-1090®, NEOCRYL BT-62®, NEOCRYL A-1079®, NEOCRYL A- 523® by the company AVECIA-NEORESINS, DOW LATEX 432® by the company DOW CHEMICAL, DAITOSOL 5000 AD® by the company DAITO KASEI KOGYO; or the aqueous dispersions of polyurethane sold under the names NEOREZ R-981®, NEOREZ R-974® by the company AVECIA-NEORESINS, AVALURE UR-405®, AVALURE UR-410®, AVALURE UR-425®, AVALURE UR -450®, SANCURE 875®, SANCURE 861®, SANCURE 878®, SANCURE 2060® by the company GOODRICH, IMPRANIL 85® by the company BAYER, AQUAMERE H-1511® by the company HYDROMER; sulfopolyesters sold under the brand name Eastman AQ by the company Eastman Chemical Products.
0108The composition according to the invention can also comprise an auxiliary film-forming agent promoting the formation of a film with the film-forming polymer.
<i><b>Charges</b></i>
0109The composition may further comprise fillers. By "fillers" is meant particles of any shape, insoluble in the medium of the composition, regardless of the temperature at which the composition is produced. These fillers can be used in particular to modify the rheology or the texture of the composition. The nature and quantity of the solid bodies depend on the mechanical properties and the desired textures.
0110By way of example of fillers, mention may be made, among others, of talc, mica, silica, kaolin, sericite, polyamide, polyethylene, polytetrafluoroethylene, polymethyl methacrylate, polyurethane powders, starch powders and silicone resin beads.
<i><b>Additional coloring matter</b></i>
0111The composition may comprise an additional coloring material, different from the composite pigment used in the present invention.
0112The additional coloring matter may be chosen from mineral pigments, organic pigments, nacres, liposoluble or water-soluble dyes.
0113The mineral pigments can be white or colored, coated or on. Mention may be made of titanium dioxide, optionally treated at the surface, zirconium or cerium oxides, as well as iron or chromium oxides, manganese violet, ultramarine blue, chromium hydrate and ferric blue. The pigments can represent from 0 to 40%, preferably from 1 to 35%, and better still from 2 to 25% of the total weight of the composition.
0114The pearlescent pigments can be chosen from white pearlescent pigments such as mica coated with titanium or bismuth oxychloride, colored pearlescent pigments such as mica titanium with iron oxides, mica titanium with especially ferric blue or chromium oxide, titanium mica with an organic pigment of the aforementioned type as well as pearlescent pigments based on bismuth oxychloride. They can represent from 0 to 20% of the total weight of the composition and better still from 0.1 to 15% (if present).
0115Among the organic pigments, mention may be made of carbon black, pigments of D & C type, and lakes based on cochineal carmine, barium, strontium, calcium, aluminum.
0116The liposoluble dyes are for example Sudan red, DC Red 17, DC Green 6, β-carotene, soybean oil, Sudan brown, DC Yellow 11, DC Violet 2, DC orange 5, quinoline yellow.
0117The water-soluble dyes are, for example, beet juice and methylene blue.
0118The dyes can represent from 0.1 to 20% of the weight of the composition and better still from 0.1 to 6% (if present).
<i><b>Other ingredients</b></i>
0119The composition can comprise at least one cosmetic or dermatological active ingredient. As cosmetic, dermatological, hygienic or pharmaceutical active agents which can be used in the compositions of the invention, mention may be made of moisturizers (polyol like glycerin), vitamins (C, A, E, F, B, or PP), essential fatty acids, essential oils, ceramides, sphingolipids, liposoluble sunscreens or in the form of nanoparticles, the specific active ingredients for skin treatment (protective agents, anti-bacterials, anti-wrinkles, etc.). These active agents can be used for example at concentrations of 0 to 20% and in particular from 0.001 to 15% relative to the total weight of the composition.
0120The cosmetic composition may also contain ingredients commonly used in cosmetics, such as for example thickeners, surfactants, trace elements, moisturizers, softeners, sequestrants, perfumes, alkalizing or acidifying agents, preservatives, antioxidants UV filters, dyes or their mixtures.
0121The composition according to the invention may comprise, depending on the type of application envisaged, the constituents conventionally used in the fields under consideration, which are present in an amount suitable for the desired dosage form.
<i><b>Dosage forms</b></i>
0122The composition can come in various forms, depending on its destination. The composition can thus be in any dosage form normally used for topical application and in particular in anhydrous form, in the form of an oily or aqueous solution, of an oily or aqueous gel, of an oil in water, water in emulsion. oil, wax in water or water in wax, of a multiple emulsion, of a dispersion of oil in water thanks to vesicles located at the oil / water interface.
0123The composition can be in the form of a cast product, in particular a stick in the case of a lipstick or a lip care product.
0124The composition can also be in various other forms, for example a more or less viscous liquid, a gel or a paste.
0125The composition can also be in the form of a solid, for example a loaf to be moistened at the time of use, so as to allow it to disintegrate.
0126The cosmetic composition can constitute a makeup composition, inter alia, a lipstick, a liquid gloss, a lipstick paste, a blush, a lip pencil, a solid or fluid foundation, an anti - dark circles or around the eyes, an eyeliner, a mascara, a nail polish, an eye shadow, a product for making up the body or the hair, or even a sun or skin coloring product.
0127The invention therefore also relates to a lipstick, liquid or solid, comprising a composition as defined above.
0128The subject of the invention is also a foundation comprising a composition as defined above.
0129The subject of the invention is also a nail varnish comprising a composition as defined above.
0130The invention also relates to a mascara comprising a composition as defined above.
0131The subject of the invention is also a product for dyeing hair fibers comprising a composition as defined above.
0132The subject of the invention is also a process for making up the skin, the lips or the integuments, in which a composition as defined above is applied to the skin, the lips or the integuments.
<i><b>EXAMPLES</b></i>
0133Cosmetic compositions comprising composite pigments with the following formulations have been produced, by way of illustration, these compositions being prepared according to the preparation methods conventionally used in cosmetics.
Example 1: Lipstick
0134A lipstick having the following composition was prepared (quantities expressed in% by mass relative to the total weight of the composition): <tables id="tabl0001" num="0001"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Polyethylene wax (Polywax 500 from BARECO)</entry><entry namest="col2" nameend="col2" align="right">8,8</entry></row><row><entry namest="col1" nameend="col1" align="left">Microcrystalline wax (SP 18 from STRAHL & PITSCH)</entry><entry namest="col2" nameend="col2" align="right">4</entry></row><row><entry namest="col1" nameend="col1" align="left">Palmitic-lauric-stearic acid triglyceride (SASOL Softisan 100)</entry><entry namest="col2" nameend="col2" align="right">5</entry></row><row><entry namest="col1" nameend="col1" align="left">Octyldodecanol</entry><entry namest="col2" nameend="col2" align="right">14,6</entry></row><row><entry namest="col1" nameend="col1" align="left">Lanolin oil</entry><entry namest="col2" nameend="col2" align="right">8,9</entry></row><row><entry namest="col1" nameend="col1" align="left">Acetylated lanolin oil</entry><entry namest="col2" nameend="col2" align="right">8,9</entry></row><row><entry namest="col1" nameend="col1" align="left">Isopropyl lanolate</entry><entry namest="col2" nameend="col2" align="right">8,9</entry></row><row><entry namest="col1" nameend="col1" align="left">Tridecyl trimellilate</entry><entry namest="col2" nameend="col2" align="right">9,7</entry></row><row><entry namest="col1" nameend="col1" align="left">Diisostearyl malate</entry><entry namest="col2" nameend="col2" align="right">12,2</entry></row><row><entry namest="col1" nameend="col1" align="left">Phenyl trimethicone (DC 556 from DOW CORNING)</entry><entry namest="col2" nameend="col2" align="right">4,0</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">TiO composite pigment<sub>2</sub>/ FD & C Blue 1 Al lake<sup>1</sup></entry><entry namest="col2" nameend="col2" align="right">15</entry></row></tbody></tgroup><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col2" align="justify"><sup>1</sup>Composite pigment consisting of 50 parts by weight of organic lacquer with the name FD&C Blue 1 Al lake per 100 parts of an inorganic core of titanium dioxide of average size 20 nm and specific surface for 50 m<sup>2</sup>/ g and produced with a polymethylhydrogenosiloxane binder.</entry></row></tbody></tgroup></table></tables>
Comparative example 1: Lipstick
0135A lipstick having the following composition, not in accordance with the invention since it was produced with only pure organic lacquer for coloring matter, was prepared (quantities expressed in% by mass relative to the total weight of the composition): <tables id="tabl0002" num="0002"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Polyethylene wax (Polywax 500 from BARECO)</entry><entry namest="col2" nameend="col2" align="right">8,8</entry></row><row><entry namest="col1" nameend="col1" align="left">Microcrystalline wax (SP 18 from STRAHL & PITSCH)</entry><entry namest="col2" nameend="col2" align="right">4</entry></row><row><entry namest="col1" nameend="col1" align="left">Palmitic-lauric-stearic acid triglyceride (SASOL Softisan 100)</entry><entry namest="col2" nameend="col2" align="right">5</entry></row><row><entry namest="col1" nameend="col1" align="left">Octyldodecanol</entry><entry namest="col2" nameend="col2" align="right">14,6</entry></row><row><entry namest="col1" nameend="col1" align="left">Lanolin oil</entry><entry namest="col2" nameend="col2" align="right">8,9</entry></row><row><entry namest="col1" nameend="col1" align="left">Acetylated lanolin oil</entry><entry namest="col2" nameend="col2" align="right">8,9</entry></row><row><entry namest="col1" nameend="col1" align="left">Isopropyl lanolate</entry><entry namest="col2" nameend="col2" align="right">8,9</entry></row><row><entry namest="col1" nameend="col1" align="left">Tridecyl trimellilate</entry><entry namest="col2" nameend="col2" align="right">9,7</entry></row><row><entry namest="col1" nameend="col1" align="left">Diisostearyl malate</entry><entry namest="col2" nameend="col2" align="right">12,2</entry></row><row><entry namest="col1" nameend="col1" align="left">Phenyl trimethicone (DC 556 from DOW CORNING)</entry><entry namest="col2" nameend="col2" align="right">4,0</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">FD&C Blue 1 Al lake<sup>2</sup></entry><entry namest="col2" nameend="col2" align="right">15</entry></row></tbody></tgroup><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col2" align="justify"><sup>2</sup>Organic lacquer with the name FD&C Blue 1 Al lake.</entry></row></tbody></tgroup></table></tables>
0136The compositions of Example 1 and Comparative Example 1 contain the same ingredients in the same proportions, except for the pigments.
0137The value of the saturation C * of the compositions which are the subject of Example 1 and of Comparative Example 1 was measured. The color difference ΔE compared to a pure pigment in the form of compacted powder was also measured.<tables id="tabl0003" num="0003"><img file="EP1586296A1_D0006.tif" /></tables>
0138The composition of Example 1 has a high saturation C * and a color little different from the color of the pure pigment in the form of compacted powder, unlike the composition of Comparative Example 1.
Example 2: Lipstick
0139A lipstick having the following composition was prepared (quantities expressed in% by mass relative to the total weight of the composition): <tables id="tabl0004" num="0004"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Polyethylene wax (Polywax 500 from BARECO)</entry><entry namest="col2" nameend="col2" align="right">8,8</entry></row><row><entry namest="col1" nameend="col1" align="left">Microcrystalline wax (SP 18 from STRAHL & PITSCH)</entry><entry namest="col2" nameend="col2" align="right">4</entry></row><row><entry namest="col1" nameend="col1" align="left">Palmitic-lauric-stearic acid triglyceride (SASOL Softisan 100)</entry><entry namest="col2" nameend="col2" align="right">5</entry></row><row><entry namest="col1" nameend="col1" align="left">Octyldodecanol</entry><entry namest="col2" nameend="col2" align="right">16,7</entry></row><row><entry namest="col1" nameend="col1" align="left">Lanolin oil</entry><entry namest="col2" nameend="col2" align="right">10,3</entry></row><row><entry namest="col1" nameend="col1" align="left">Acetylated lanolin oil</entry><entry namest="col2" nameend="col2" align="right">10,3</entry></row><row><entry namest="col1" nameend="col1" align="left">Isopropyl lanolate</entry><entry namest="col2" nameend="col2" align="right">10,3</entry></row><row><entry namest="col1" nameend="col1" align="left">Tridecyl trimellilate</entry><entry namest="col2" nameend="col2" align="right">11,1</entry></row><row><entry namest="col1" nameend="col1" align="left">Diisostearyl malate</entry><entry namest="col2" nameend="col2" align="right">14,0</entry></row><row><entry namest="col1" nameend="col1" align="left">Phenyl trimethicone (DC 556 from DOW CORNING)</entry><entry namest="col2" nameend="col2" align="right">4,5</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">TiO composite pigment<sub>2</sub>/ FD & C Blue 1 Al lake <sup>1</sup></entry><entry namest="col2" nameend="col2" align="right">5</entry></row></tbody></tgroup><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col2" align="justify"><sup>1</sup>Composite pigment consisting of 50 parts by weight of organic lacquer with the name FD&C Blue 1 Al lake per 100 parts of an inorganic core of titanium dioxide of average size 20 nm and specific surface for 50 m<sup>2</sup>/ g and produced with a polymethylhydrogenosiloxane binder.</entry></row></tbody></tgroup></table></tables>
Comparative example 2: Lipstick
0140A lipstick having the following composition, not in accordance with the invention since it was produced with only pure organic lacquer for coloring matter, was prepared (quantities expressed in% by mass relative to the total weight of the composition): <tables id="tabl0005" num="0005"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Polyethylene wax (Polywax 500 from BARECO)</entry><entry namest="col2" nameend="col2" align="right">8,8</entry></row><row><entry namest="col1" nameend="col1" align="left">Microcrystalline wax (SP 18 from STRAHL & PITSCH)</entry><entry namest="col2" nameend="col2" align="right">4</entry></row><row><entry namest="col1" nameend="col1" align="left">Palmitic-lauric-stearic acid triglyceride (SASOL Softisan 100)</entry><entry namest="col2" nameend="col2" align="right">5</entry></row><row><entry namest="col1" nameend="col1" align="left">Octyldodecanol</entry><entry namest="col2" nameend="col2" align="right">16,7</entry></row><row><entry namest="col1" nameend="col1" align="left">Lanolin oil</entry><entry namest="col2" nameend="col2" align="right">10,3</entry></row><row><entry namest="col1" nameend="col1" align="left">Acetylated lanolin oil</entry><entry namest="col2" nameend="col2" align="right">10,3</entry></row><row><entry namest="col1" nameend="col1" align="left">Isopropyl lanolate</entry><entry namest="col2" nameend="col2" align="right">10,3</entry></row><row><entry namest="col1" nameend="col1" align="left">Tridecyl trimellilate</entry><entry namest="col2" nameend="col2" align="right">11,1</entry></row><row><entry namest="col1" nameend="col1" align="left">Diisostearyl malate</entry><entry namest="col2" nameend="col2" align="right">14,0</entry></row><row><entry namest="col1" nameend="col1" align="left">Phenyl trimethicone (DC 556 from DOW CORNING)</entry><entry namest="col2" nameend="col2" align="right">4,5</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">FD&C Blue 1 Al lake<sup>2</sup></entry><entry namest="col2" nameend="col2" align="right">5</entry></row></tbody></tgroup><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col2" align="justify"><sup>2</sup>Organic lacquer of denomination FD&C Blue 1 Al lake.</entry></row></tbody></tgroup></table></tables>
0141The compositions of Example 2 and Comparative Example 2 contain the same ingredients in the same proportions, except for the pigments.
0142The covering power and the saturation C * of the compositions of Example 2 and Comparative Example 2 were measured.<tables id="tabl0006" num="0006"><img file="EP1586296A1_D0007.tif" /></tables>
0143The covering power and the saturation C * have significantly higher values for the composition of Example 2 than for that of Comparative Example 2.
Example 3: Foundation
0144A foundation having the following composition was prepared (quantities expressed in% by weight relative to the total weight of the composition): <tables id="tabl0007" num="0007"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Dimethicone copolyol (KF 6017 from ka company SHIN ETSU)</entry><entry namest="col2" nameend="col2" align="right">5</entry></row><row><entry namest="col1" nameend="col1" align="left">Dimethicone (DC 200 Fluid from DOW CORNING)</entry><entry namest="col2" nameend="col2" align="right">4</entry></row><row><entry namest="col1" nameend="col1" align="left">Cyclomethicone</entry><entry namest="col2" nameend="col2" align="right">15</entry></row><row><entry namest="col1" nameend="col1" align="left">Isododecane</entry><entry namest="col2" nameend="col2" align="right">10</entry></row><row><entry namest="col1" nameend="col1" align="left">Bentone gel (Bentone gel VS5V from ELEMENTIS)</entry><entry namest="col2" nameend="col2" align="right">10</entry></row><row><entry namest="col1" nameend="col1" align="left">Plastic Powder D400<sup>3</sup></entry><entry namest="col2" nameend="col2" align="right">4</entry></row><row><entry namest="col1" nameend="col1" align="left">Titanium oxide coated with aluminum stearoyl glutamate<sup>4</sup></entry><entry namest="col2" nameend="col2" align="right">6,61</entry></row><row><entry namest="col1" nameend="col1" align="left">Yellow iron oxide coated with aluminum stearoyl glutamate<sup>4</sup></entry><entry namest="col2" nameend="col2" align="right">0,95</entry></row><row><entry namest="col1" nameend="col1" align="left">Black iron oxide coated with aluminum stearoyl glutamate<sup>5</sup></entry><entry namest="col2" nameend="col2" align="right">0,12</entry></row><row><entry namest="col1" nameend="col1" align="left">TiO composite pigment<sub>2</sub>/ D & C Red N ° 7<sup>5</sup></entry><entry namest="col2" nameend="col2" align="right">0,32</entry></row><row><entry namest="col1" nameend="col1" align="left">Water</entry><entry namest="col2" nameend="col2" align="right">33,2</entry></row><row><entry namest="col1" nameend="col1" align="left">Butylene glycol</entry><entry namest="col2" nameend="col2" align="right">10</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Magnesium sulfate</entry><entry namest="col2" nameend="col2" align="right">0,8</entry></row></tbody></tgroup><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col2" align="justify"><sup>3</sup>marketed by TOSHIKI PIGMENT</entry></row><row><entry namest="col1" nameend="col2" align="justify"><sup>4</sup>marketed by MIYOSHI</entry></row><row><entry namest="col1" nameend="col2" align="justify"><sup>5</sup>composite pigment consisting of 50 parts by weight of organic pigment D&C Red N ° 7 per 100 parts of an inorganic nucleus of titanium dioxide of average size 20 nm and specific surface 50 m<sup>2</sup>/ g and produced with a polymethylhydrogenosiloxane binder.</entry></row></tbody></tgroup></table></tables>
Comparative example 3: Foundation
0145A foundation having the following composition, not in accordance with the invention since it is devoid of composite pigment, was prepared (quantities expressed in% by weight relative to the total weight of the composition): <tables id="tabl0008" num="0008"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Dimethicone copolyol (KF 6017 from ka company SHUI ETSU)</entry><entry namest="col2" nameend="col2" align="right">5</entry></row><row><entry namest="col1" nameend="col1" align="left">Dimethicone (DC 200 Fluid from DOW CORNING)</entry><entry namest="col2" nameend="col2" align="right">4</entry></row><row><entry namest="col1" nameend="col1" align="left">Cyclomethicone</entry><entry namest="col2" nameend="col2" align="right">15</entry></row><row><entry namest="col1" nameend="col1" align="left">Isododecane</entry><entry namest="col2" nameend="col2" align="right">10</entry></row><row><entry namest="col1" nameend="col1" align="left">Bentone gel (Bentone salt VS5V from ELEMENTIS)</entry><entry namest="col2" nameend="col2" align="right">10</entry></row><row><entry namest="col1" nameend="col1" align="left">Plastic Powder D400<sup>3</sup></entry><entry namest="col2" nameend="col2" align="right">4</entry></row><row><entry namest="col1" nameend="col1" align="left">Titanium oxide coated with aluminum stearoyl glutamate<sup>4</sup></entry><entry namest="col2" nameend="col2" align="right">6,61</entry></row><row><entry namest="col1" nameend="col1" align="left">Yellow iron oxide coated with aluminum stearoyl glutamate<sup>4</sup></entry><entry namest="col2" nameend="col2" align="right">0,95</entry></row><row><entry namest="col1" nameend="col1" align="left">Black iron oxide coated with aluminum stearoyl glutamate<sup>4</sup></entry><entry namest="col2" nameend="col2" align="right">0,12</entry></row><row><entry namest="col1" nameend="col1" align="left">Red iron oxide coated with aluminum stearoyl glutamate<sup>4</sup></entry><entry namest="col2" nameend="col2" align="right">0,32</entry></row><row><entry namest="col1" nameend="col1" align="left">Water</entry><entry namest="col2" nameend="col2" align="right">33,2</entry></row><row><entry namest="col1" nameend="col1" align="left">Butylene glycol</entry><entry namest="col2" nameend="col2" align="right">10</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Magnesium sulfate</entry><entry namest="col2" nameend="col2" align="right">0,8</entry></row></tbody></tgroup><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col2" align="justify"><sup>3</sup>marketed by TOSHIKI PIGMENT</entry></row><row><entry namest="col1" nameend="col2" align="justify"><sup>4</sup>marketed by MIYOSHI</entry></row></tbody></tgroup></table></tables>
0146The compositions of Example 3 and Comparative Example 3 contain the same ingredients in the same proportions, except for the pigments.
0147The covering power and the saturation C * of the compositions of Example 3 and Comparative Example 3 were measured.<tables id="tabl0009" num="0009"><img file="EP1586296A1_D0008.tif" /></tables>
0148The covering power and the saturation C * of the composition of Example 3 are higher than those of the composition of Comparative Example 3.
0149Of course, the invention is not limited to the examples which have just been given.
0150The intervals given must be included, limits included, unless otherwise specified.
0151Throughout the description, including the claims, the expression "comprising a" should be understood as being synonymous with "comprising at least one", unless otherwise specified.
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| EP0581651A2 | Cites | European Patent Office (EPO) | A | Search report | 1,8,19-32 |
| EP0587908A1 | Cites | European Patent Office (EPO) | X | Search report | 1,4-8,10-15,19-22,28,40-47 |
| EP1184426A2 | Cites | European Patent Office (EPO) | A | Search report | 1,16-30,33-38 |
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| EP1433462A1 | Cites | European Patent Office (EPO) | PX | Search report | 1-9,19-32,40-50 |
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| JP5291500B2 | Japan | B2 | |
| ES2428359T3 | Spain | T3 | |
| BR0315032B1 | Brazil | B1 | |
| JP2015131851A | Japan | A | |
| JP5756251B2 | Japan | B2 | |
| EP1586296B1 | European Patent Office (EPO) | B1 | |
| ES2575512T3 | Spain | T3 | |
| EP1763330B1 | European Patent Office (EPO) | B1 | |
| JP6092495B2 | Japan | B2 | |
| EP1586295B1 | European Patent Office (EPO) | B1 | |
| ES2623079T3 | Spain | T3 | |
| ES2634529T3 | Spain | T3 | |
| BRPI0501247B1 | Brazil | B1 | |
| BRPI0502367B1 | Brazil | B1 | |
| BRPI0502154B1 | Brazil | B1 |
75 legal events, as 10 offices reported them to INPADOC
Over the term
Point at a mark for the eventEvents
| Event | Code | Office | |
|---|---|---|---|
| Gb: european patent ceased through non-payment of renewal feeCeasedGBPC | GBPC | EP | |
| Application deemed withdrawn, or ip right lapsed, due to non-payment of renewal feeWithdrawnR119 | R119 | DE | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Fee paymentPLFP | PLFP | FR | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Fee paymentPLFP | PLFP | FR | |
| No opposition filedOpposition26N | 26N | EP | |
| No opposition filed within time limitOppositionORIGINAL CODE: 0009261PLBE | PLBE | EP | |
| Information on the status of an ep patent application or granted ep patentGrantedSTATUS: NO OPPOSITION FILED WITHIN TIME LIMITSTAA | STAA | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Patent lapsedLapsedMM4A | MM4A | IE | |
| No opposition filed against granted patent, or epo opposition proceedings concluded without decisionGrantedR097 | R097 | DE | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Patent ceasedCeasedPL | PL | CH | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Deletion acc. to par. 5 (withdrawal of the translation of the ep patent)MK05 | MK05 | AT | |
| Patent invalid in the netherlands as no translation has been filedMP | MP | NL | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Invalidated european patentMG4D | MG4D | LT | |
| Definitive protectionFG2A | FG2A | ES | |
| Dpma publication of mentioned ep patent grantGrantedR096 | R096 | DE | |
| Fee paymentPLFP | PLFP | FR | |
| European patents granted designating irelandGrantedLANGUAGE OF EP DOCUMENT: FRENCHFG4D | FG4D | IE | |
| Reference to at number (ep patent validated in austria)REF | REF | AT | |
| European patent takes effect as a national patent in ch/liEP | EP | CH | |
| Designated contracting statesAK | AK | EP | |
| European patent grantedGrantedNOT ENGLISHFG4D | FG4D | GB | |
| (expected) grantORIGINAL CODE: 0009210GRAA | GRAA | EP | |
| Intention to grant announcedINTG | INTG | EP | |
| Grant fee paidORIGINAL CODE: EPIDOSNIGR3GRAS | GRAS | EP | |
| Intention to grant announcedINTG | INTG | EP | |
| Despatch of communication of intention to grant a patentORIGINAL CODE: EPIDOSNIGR1GRAP | GRAP | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Amendment of ipc main classPREVIOUS MAIN CLASS: A61K0007025000R079 | R079 | DE | |
| First examination report despatched17Q | 17Q | EP | |
| Designation fees paidAKX | AKX | EP | |
| Request for examination filed17P | 17P | EP | |
| Designated contracting statesAK | AK | EP | |
| Request for extension of the european patentAX | AX | EP | |
| Public reference made under article 153(3) epc to a published international application that has entered the european phaseORIGINAL CODE: 0009012PUAI | PUAI | EP |
Numbers
- Publication
- 1586296
- Publication, DOCDB
- 1586296
- Publication, EPODOC
- EP1586296
- Application
- 5300266
- Application, DOCDB
- 05300266
- Application, EPODOC
- EP20050300266
Titles3
- German
- Kosmetische Zusammensetzung für die Haut, die Lippen und/oder die Fingernägel
- English
- Cosmetic composition for application to the skin, lips and/or nails.
- French
- Composition destinée à être appliquée sur la peau, les lèvres et/ou les phanères.
Classification
- CPC, 16
- A61Q1/00
- A61K8/0241
- A61K8/11
- A61K8/19
- A61K8/25
- A61K8/29
- A61K8/445
- A61K2800/412
- A61K2800/43
- A61K2800/436
- A61K2800/623
- A61Q1/02
- A61Q1/06
- A61Q1/10
- A61Q3/02
- A61Q5/10
- IPC, 19
- A61K8 25
- A61K8 00
- A61K8 02
- A61K8 04
- A61K8 11
- A61K8 18
- A61K8 19
- A61K8 26
- A61K8 29
- A61K8 44
- A61Q1 00
- A61Q1 02
- A61Q1 04
- A61Q1 06
- A61Q1 10
- A61Q1 12
- A61Q3 00
- A61Q3 02
- A61Q5 10
Designated states2
- Contracting states, 1
- Türkiye
- Extension states, 1
- Yugoslavia, later Serbia and Montenegro (until 2006)