EP4572856A1 - A long-wear facial composition - Google Patents
A long-wear facial compositionInfo
- Publication number
- EP4572856A1 EP4572856A1 EP23755089.2A EP23755089A EP4572856A1 EP 4572856 A1 EP4572856 A1 EP 4572856A1 EP 23755089 A EP23755089 A EP 23755089A EP 4572856 A1 EP4572856 A1 EP 4572856A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- skin
- weight
- range
- present
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/60—Sugars; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/735—Mucopolysaccharides, e.g. hyaluronic acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/007—Preparations for dry skin
Definitions
- the present invention relates to a facial composition. It more particularly relates to colour cosmetics such as facial foundations especially long-wear compositions that comprise resin and humectant.
- a composition for face such as a facial foundation is used to get a perfect skin tone and desired color and as a base for further application of make-up.
- the foundations have their own set of problems such as dry patches of foundation, the skin getting too shiny or oily, wearing off of foundation within a few hours.
- As foundations are used as base for further application of make-up if the foundation is not proper, everything built on top of it will be wobbly and compromised and result in overall undesirable appearance.
- Facial foundations are used in cosmetology to provide bases for obtaining proper adhesion of powder and pigments to skin.
- Such compositions comprise a mixture of oils, fats, waxes and the like in which there have been uniformly dispersed dry powders, such as talc, and pigments.
- the facial foundations now in use have poor wear and color stability so that in a few hours after the application the preparation begins to wear off the skin and to change color ("orange out”). These effects result from the interaction of perspiration, skin oils and surface moisture of the skin with the oils, pigments and powders in the foundation.
- pigments especially inorganic pigments
- inorganic pigments such as titanium oxides (dioxides or the like) and iron oxides and the like
- the present invention relates to a facial cosmetic composition
- a facial cosmetic composition comprising: a.
- a silicone resin comprising 1 to 8 wt% by weight of the composition, the resin comprising a silsesquioxane derivative and a siloxysilicate derivative,
- a humectant in the range of 0.01 to 10 wt% comprising a saccharide based and a glucosamine glycan based moisturizing agent; andwherein, the composition further comprises a thixotropic agent in the range of 0.01 to 10 wt% by weight of the composition.
- any particular upper concentration can be associated with any particular lower concentration or amount.
- the present invention relates to a facial composition. It more particularly relates to flowable colour cosmetics such as facial foundations especially long-wear compositions that comprise resin and humectant.
- the present invention provides a facial cosmetic composition
- a facial cosmetic composition comprising: a. A silicone resin comprising 1 to 8 wt% by weight of the composition, the resin comprising a silsesquioxane derivative and a siloxysilicate derivative, b. A humectant in the range of 0.01 to 10 wt% comprising a saccharide based and a glucosamine glycan based moisturizing agent; and wherein, the composition further comprises a thixotropic agent in the range of 0.01 to 10 wt% by weight of the composition.
- the present invention delivers all the three parameters without compromising on any of them.
- the present inventors surprisingly found that the composition of the present invention was able to have high pigment loading, even as high as 45% and still the facial composition was able to give a stable appearance on the skin for long hours as long as 10 hrs, 12 hrs, 15 hrs, 20 hrs or even 24 hours. It was also surprising finding of the present invention that the skin remained moisturized during the time that the facial composition remained on the skin and even after the removal of the facial composition. As it is usually seen that long stay colour pigment loaded facial compositions of foundations usually dry the skin during the time of their stay on the skin and after removal.
- the present invention provides a facial cosmetic composition and more particularly a facial foundation composition which is preferably flowable and more preferably a liquid composition.
- the composition is capable of coloured pigment loading.
- composition of the present invention is intended for use as a foundation.
- foundation it is meant that the composition is used as a base or a pre-makeup base on the face before makeup is applied.
- the foundation can also be used to even out the skin tone and/or to conceal any flaws and give a uniform appearance to the face.
- the composition of the present invention comprises a silicone resin and a humectant.
- the silicone resin comprises a silsesquioxane derivative, a siloxysilicate derivative, and mixtures and combinations thereof.
- the humectant comprises a saccharide based and a glucosamine glycan based moisturizing agent.
- Silicone resins are a type of silicone material which is formed by branched, cagelike oligosiloxanes with the general formula of R n SiX m O y , where R is a non reactive substituent, usually Methyl (Me) or Phenyl (Ph), and X is a functional group Hydrogen (H), Hydroxyl group (OH), Chlorine (Cl) or Alkoxy group (OR).
- Silicone resin are known in the art as "MDTQ” nomenclature, whereby a silicone resin is described according to the various monomeric siloxane units which make up the polymer. Each letter of "MDTQ” denotes a different type of unit. The letter M denotes the monofunctional unit (CHshSiO. This unit is considered to be monofunctional because the silicone atom only shares one oxygen when the unit is part of a polymer.
- the "M” unit can be represented by the following structure:
- At least one of the methyl groups of the M unit may be replaced by another group, e.g., to give a unit with formula [R(CHs)2]SiO, as represented in the following structure: wherein R is chosen from groups other than methyl groups.
- groups other than methyl groups include alkyl groups other than methyl groups, alkene groups, alkyne groups, hydroxyl groups, thiol groups, ester groups, acid groups, ether groups, wherein the groups other than methyl groups may be further substituted.
- the symbol D denotes the difunctional unit (CH3)2SiO2 wherein two oxygen atoms bonded to the silicone atom are used for binding to the rest of the polymer.
- the "D" unit which is the major building block of dimethicone oils, can be represented as:
- At least one of the methyl groups of the D unit may be replaced by another group, e.g., to give a unit with formula [R(CH 3 )2]SiC>2.
- T denotes the trifunctional unit, (CH 3 )SiO3 and can be represented as: At least one of the methyl groups of the T unit may be replaced by another group.
- Q denotes the tetrafunctional unit, SiC wherein all four oxygens bonded to the silicone atom are bonded to the rest of the polymer.
- Silicone polymers used for the purposes of the present invention may include silanes, siloxanes, siloxysilicates, and silsesquioxanes.
- a preferable example of a silsesquioxane is Polymethylsilsesquioxanes (PMSQ). Polymethylsilsesquioxanes are silsesquioxanes that do not have a substituent replacing the methyl groups.
- a preferable example of a siloxysilicate is trimethylsiloxysilicate.
- the silicone resin comprises at least one silicone resin selected from group consisting of siloxysilicate, silsesquioxane or other silicone polymers.
- silicone resins are but not limited to, for example, MQ resins (for example, trimethylsiloxysilicates), T-propyl silsesquioxanes and MK resins (for example, polymethylsilsesquioxanes).
- the ratio of silsesquioxane derivative to siloxysilicate derivative in the composition of the present invention is in the range of 1:99 to 99:1.
- the present invention comprises a silicone resin comprising a silsesquioxane derivative. It is preferred that the silsesquioxane derivative is in the range from 0.5 to 7 wt% more preferably from 1 to 7 wt%, even more preferably from 1 to 6 wt%, furthermore preferably from 1 to 5 wt%, yet more preferably from 1 to 4 wt%, still more preferably from 1 to 3 wt% and still even more preferably from 1 to 2 wt% by weight of the composition.
- the silsesquioxane derivative is in the range of 0.01 to 99.99 wt% more preferably from 1 to 90 wt%, even more preferably from 1 to 80 wt%, furthermore preferably from 1 to 70 wt% and still more preferably from 1 to 50 wt% by weight of the silicone resin.
- Highly preferred silsesquioxane derivative are polysilsesquioxanes of formula (CHsSiO3/2)n (units T) in which n is greater than 100 and at least one of the methyl radicals of which may be substituted with a group R.
- silsesquioxane polymethylsilsesquioxane (PMSQ).
- PMSQs are silsesquioxanes that do not have a substituent replacing the methyl groups.
- Siloxysilicate derivative is silsesquioxanes that do not have a substituent replacing the methyl groups.
- the present invention comprises a silicone resin comprising a siloxysilicate derivative. It is preferred that the siloxysilicate derivative is in the range from 0.5 to 7 wt% by weight of the composition, more preferably from 1 to 7 wt%, even more preferably from 1 to 6 wt%, furthermore preferably from 1 to 5 wt%, yet more preferably from 1 to 4 wt%, still more preferably from 1 to 3 wt% and still even more preferably from 1 to 2 wt% by weight of the composition.
- the siloxysilicate derivative is in the range of 0.01 to 99.99 wt% more preferably from 1 to 90 wt%, even more preferably from 1 to 80 wt%, furthermore preferably from 1 to 70 wt% and still more preferably from 1 to 50 wt% by weight of the silicone resin.
- MQ resins Such resins are sometimes referred to as "MQ resins" because of the presence of the monovalent (M) siloxane units and the quadrivalent or tetravalent (Q) silicon dioxide units.
- MQ resins monovalent (M) siloxane units and the quadrivalent or tetravalent (Q) silicon dioxide units.
- R and R 2 may be either a phenyl group or a C1 -C12 alkyl group and both
- M 1 and M 2 are independently selected from the group consisting of phenyl, phenethyl, polyether, hydrogen and C1-C23 alkyl group (which may also include halogen substituted hydrocarbon radicals) and wherein x, y and z satisfy the following relationship: 0.5 ⁇ (x+y)/z ⁇ 4.0 and one of x and y may be zero.
- the siloxysilicate derivative is Trimethylsiloxysilicate (TMSS).
- TMSS Trimethylsiloxysilicate
- the composition comprises total amount of a silsesquioxane derivative and a siloxysilicate derivative in the range from 1 to 8 wt%, preferably from 2 to 7 wt%, even more preferably from 3 to 6 wt% and further more preferably from 4 to 5 wt%.
- composition with low levels of silicone resin is effective as a long wear composition as it is well known in the makeup industry that only high silicone resin work to achieve a long wear facial cosmetic composition.
- silicone resin in amounts less than or equal to 8 wt% by weight of the composition. In other words, it is preferably meant that silicone resin amounts are not exceeding 8 wt% by weight of the composition.
- high levels in the context of silicone resin, it is preferably meant that silicone resin amounts are exceeding 8 wt% by weight of the composition.
- the present invention comprises a humectant preferably in the range of 0.01 to 10 wt% by weight of the composition.
- a humectant as understood in the art helps to reduce loss of moisture for the skin.
- the humectant of the present invention comprises a saccharide based and a glucosamine glycan based moisturizing agent.
- the ratio of saccharide based moisturizing agent to glucosamine glycan based moisturizing agent is in the range of 1 :99 to 99:1.
- the present invention comprises a humectant comprising a saccharide-based moisturizing agent. It is preferred that the saccharide based moisturizing agent is in the range of 0.01 to 10 wt% by weight of the composition. It is further preferred that the saccharide based moisturizing agent is in the range of 0.01 to 99.99 wt% by weight of the humectant.
- the composition comprises saccharide based moisturizing agent in amounts from 0.001 to 10 wt%, more preferably from 0.01 to 8 wt%, even more preferably from 0.1 to 7 wt%, furthermore preferably from 0.1 to 5 wt% and still more preferably from 0.1 to 3 wt% by weight of the composition.
- saccharide based moisturizing agent of the present invention is Saccharide isomerate.
- the composition comprises Saccharide isomerate in amounts from 0.001 to 10 wt%, more preferably from 0.01 to 8 wt%, even more preferably from 0.1 to 7 wt%, furthermore preferably from 0.1 to 5 wt% and still more preferably from 0.1 to 3 wt% by weight of the composition.
- Saccharide isomerate is a complex mixture of hydrating corn-derived sugars which have moisture-binding (humectant) properties.
- the sugars are then isomerized, a process in which rearranges molecular structure to change the way a substance works and/or the results it has.
- the result closely matches the carbohydrates naturally present in skin’s natural moisturizing factor, NMF.
- Saccharide isomerate is commercially available under trade name ‘Pentavitin®’ (from DSM), under trade name Waterin (from Clariant), under trade names ‘EPS3 Powder’, ‘EPS4 Powder’, ‘EPS5 Powder’ and‘EPS15 Powder’ (all from Codif) and under trade name'Hyanify’ (from Lipotec S.A.).
- Glucosamine glycan based moisturizing agent Glucosamine glycan based moisturizing agent
- the present invention comprises a humectant comprising a glucosamine glycan based moisturizing agent. It is preferred that the glucosamine glycan based moisturizing agent is in the range of 0.01 to 10 wt% by weight of the composition. It is further preferred that the glucosamine glycan based moisturizing agent is in the range of 0.01 to 99.99 wt% by weight of the humectant.
- the composition comprises glucosamine glycan based moisturizing agent in amounts from 0.001 to 10 wt%, more preferably from 0.01 to 8 wt%, even more preferably from 0.1 to 7 wt%, furthermore preferably from 0.1 to 5 wt% and still more preferably from 0.1 to 3 wt% by weight of the composition.
- the glucosamine glycan based moisturizing agent of the present invention is a hyaluronate or a hyaluronic acid derivative.
- hyaluronic acid also referred to as "HY” hereinafter
- HY hyaluronic acid
- the composition comprises hyaluronate derivative in amounts from 0.001 to 10 wt%, more preferably from 0.01 to 8 wt%, even more preferably from 0.1 to 7 wt%, further more preferably from 0.1 to 5 wt% and still more preferably from 0.1 to 3 wt% by weight of the composition.
- the glucosamine glycan based moisturizing agent is a hyaluronate derivative.
- Thixotropy is a characteristic feature of certain gels or fluids that exist in viscous form under normal conditions, but start flowing (become thin, less viscous) when shaken or agitated.
- Thixotropic agents are those that stimulate the process of thixotropy.
- the present invention comprises a thixotropic agent in the range of 0.01 to 10 wt% by weight of the composition more preferably from 0.01 to 8 wt%, even more preferably from 0.1 to 7 wt%, furthermore preferably from 0.1 to 5 wt% and still more preferably from 0.1 to 3 wt% by weight of the composition.
- the thixotropic agent of the present invention comprises a lipophilic clay.
- lipophilic clay is intended to mean any clay that is liposoluble or lipodispersible in the oily phase of the composition.
- the clay denotes a material based on hydrated silicates and/or aluminosilicates, of lamellar structure.
- the clays can be natural or synthetic and they are rendered lipophilic by treatment with an alkylammonium salt, such as a Cw to C22 ammonium chloride, in particular stearalkonium chloride or distearyldimethylammonium chloride.
- They may be chosen from bentonites, in particular bentonites, hectorites and montmorillonites, beidellites, saponites, nontronites, sepiolites, biotites, attapulgites, vermiculites and zeolites.
- hectorites and bentonites are preferably chosen from hectorites and bentonites, and most preferably bentonites.
- a lipophilic clay chosen from hydrophobically modified bentonites and hydrophobically modified hectorites, in particular modified with a C10 to C22 quaternary ammonium chloride.
- An example of hectorite that may be used as a thixotropic agent in the compositions of the present invention include Disteardimonium Hectorite, commercially available as BENTON E GEL® VS-5 PC V.
- the thixotropic agent is an activated thixotropic agent.
- compositions of the present invention comprise an antioxidant capable of reversing or preventing free radicals from causing oxidative stress.
- the present composition further comprises an antioxidant compound in the range of 0.01 to 10 wt% more preferably from 0.01 to 8 wt%, even more preferably from 0.1 to 7 wt%, further more preferably from 0.1 to 5 wt% and still more preferably from 0.1 to 3 wt% by weight of the composition.
- the antioxidants for the purposes of this invention are preferably selected from the group of Vitamin B3 (niacinamide), selenium, Coenzyme Q10, Vitamin C, Vitamin E, polyphenol, resveratrol.
- the most preferred antioxidants for the present invention are the vitamin-based antioxidant and among those Vitamin B3 and C are highly preferred.
- a suitable base is used to prepare the cosmetic composition of the present invention.
- Formulation base may be water. It is preferred that the base is emulsion, preferably oil- in-water, water-in oil and silicone invert emulsions, and most preferably silicone invert emulsions (W/Si emulsion).
- the present composition comprises a formulation base in the range of 10 to 40 wt%, more preferably 12 to 35wt% and most preferably in the range of 15 to 30wt%.
- Light emollients having low viscosity preferably less than 50cp may be used for the composition of the present invention.
- the common light emollients known in the industry can be used, preferably volatile emollients e.g. cyclopentasiloxane, having flash point less than 150°C.
- the present composition comprises light emollients in the range of 10 to 40 wt%, more preferably 12 to 35wt% and most preferably in the range of 15 to 30wt%.
- compositions of the present invention are capable of pigment loading in the range of 10 to 45 wt%, more preferably 15 to 45 wt%, further preferably in the range of 20 to 45 wt% and most preferably in the range of 25 to 45%wt%. It is preferred that the pigments are inorganic pigments and most preferably metal oxides or derivatives thereof.
- the present invention provides use of composition for manufacture of a cosmetic composition in loading pigment upto 45wt% of the composition.
- the present composition provides at least 20wt% of pigment loading, more preferably at least 25wt%, 26wt%, 27wt%, 28wt%, 29wt%, 30wt%, 31wt%, 32wt%, 33wt%, 34wt%,35wt%, 36wt%, 3wt5, 38wt%, 39wt%, 40wt%, 41wt%, 42wt%, 43wt%, 44wt%, and most preferably at least 45wt% by weight of the composition.
- the inorganic powder used as an extender includes silicic acids such as silicic anhydride, silicic hydride and the like; silicates such as aluminum silicate, magnesium silicate and the like; clay minerals such as talc, kaolin, bentonite, mica, sericite and the like; phosphate minerals such as hydroxyapatite and the like; metal oxides such as aluminum oxide, magnesium oxide and the like; carbonates of alkaline earth metal such as light calcium carbonate, heavy calcium carbonate, light magnesium carbonate, heavy magnesium carbonate and the like; sulfates of alkaline earth metal such as magnesium sulfate, barium sulfate (platy barium sulfate, butterfly barium sulfate etc.) and the like; boron nitride and the like.
- silicic acids such as silicic anhydride, silicic hydride and the like
- silicates such as aluminum silicate, magnesium silicate and the like
- clay minerals such as tal
- the inorganic powder used as a UV scattering agent or white pigment includes zirconium oxide, zinc oxide, zinc oxide fine particles, titanium oxide, titanium oxide fine particles and the like, and the inorganic powder used as a pearlescent pigment includes titanium mica, titanium oxide-coated barium sulfate, bismuth oxychloride and the like.
- the inorganic powder used as a coloration pigment includes red iron oxide, yellow iron oxide, black iron oxide, chrome oxide, chromium hydroxide, cobalt oxide, carbon black, ultramarine blue, iron blue and the like.
- compositions of the present invention can include numerous cosmetically acceptable ingredients selected for various desirable effects. These ingredients can be either in dry or liquid form, however, at levels that do not detract from the primary objects of the present invention.
- Pigments are used in the present invention. Pigments may be selected from a large group of materials to numerous to mention herein. Included in this group are inorganic pigments, organic pigments, and pearlescent pigments. When employed, the pigments are present in proportions depending on the color and the intensity of the color which it is intended to produce. Pigments can be used in the present invention at levels from about 0.1% to about 45%, preferably from about 5 % to about 40% and most preferably from 10 to 40wt%.
- Pigments are selected from the group consisting of inorganic pigments, organic lake pigments, pearlesent pigments, and mixtures thereof. Said pigments may optionally be surface-treated with a large number of materials that include, but, not limited to silicones, perfluorinated compounds, lecithin, amino acids, lauroyllisine, teflon, and esters. Included are the pigments as disclosed in U.S. Pat. Nos. 5,368.639 and 5,458,681, both to Hasegawa et at, issued Nov. 29, 1994 and Oct. 17, 1995; both herein incorporated by reference.
- Inorganic pigments useful in the present invention include those selected from the group consisting of rutile or anatase titanium dioxide, coded in the Color Index under the reference C 77,891; black, yellow, red and brown iron oxides, ceded under references CIT7.499, 77,492 and, 77.491; manganese violet (CIT7.742); ultramarine blue (CI77.007); chromium oxide (Cl 77,288); chromium hydrate (CI77.289); and ferric blue (Cl 77.510) and mixtures thereof.
- the organic pigments and lakes useful in the present invention include those selected from the group consisting of D&C Red No. 19 (Cl 45,170), D&C Red No.
- the pearlescent pigments useful in the present invention include those selected from the group consisting of the white pearlescent pigments such as mica coated with titanium oxide, bismuth oxychloride, colored pearlescent pigments such as titanium mica with iron oxides, titanium mica with ferric blue, chromium oxide and the like, titanium mica with an organic pigment of the above-mentioned type as well as those based on bismuth oxychloride and mixtures thereof. Any optional ingredients known to those skilled in the art may also be used in the invention.
- optional ingredients are disclosed in CTFA Cosmetic Ingredient Handbook, Second Edition, 1992, pages 621-622, 623-626 and 637-639; incorporated herein by reference.
- Some of the more frequently used components include from about 1% to about 10% fillers and powders other than talc, including but not limited to the group consisting of treated and untreated mica, nylon, polyethylene, silica, polymethacrylate., kaolin, teflon, starch, oil absorbers and mixtures thereof.
- liquid ingredients including, but not limited to the group consisting of silicone oils; long chained fatty acid esters; glycerides; water; fragrances; skin condi tioning and protective materials including, botanical or biological products as disclosed in The CTFA, Cosmetic Ingredient Handbook, Second Edition, pages 493-496; herein incorporated by reference.
- Other skin conditioning and protective material include, but, are not limited to panthenol, allantoin, aloe, aloeveragel, PABA, tocopheryl; and mixtures thereof.
- cos metic preservatives including, but not limited to the group consisting of methylparaben, propylparaben, butylparaben, ethylparaben, potassium sorbate, trisodium EDTA, phenoxyethanol, ethyl alcohol, diazolidinyl urea, imidazo lidinyl urea, quaternium-15 and mixtures thereof.
- composition of the invention may be obtained according to the preparation processes conventionally used in cosmetics or dermatology.
- the process of manufacture of the composition of the present invention comprises steps of taking the oil phase ingredients such as light emollients and resins; adding thixotropic agent; adding the pigments and making up with water and minors.
- the present invention provides a composition that is used as a makeup base, a foundation.
- the composition can be used to give an even tone to the skin on application.
- the composition of the present invention provides skin moisturization for at least 6 hours, and can provide skin moisturization upto 8 hours, 10 hours, 12 hours, 14 hours, 16 hours, 18 hours, 20 hours, 22 hours and upto 24 hours.
- the present invention provides use of composition for manufacture of a cosmetic composition in loading pigment upto 45wt% of the composition.
- the present invention provides use of composition for manufacture of a cosmetic composition in loading pigment upto 45wt% of the composition. It is preferable that the present composition provides at least 20wt% of pigment loading, more preferably at least 25wt%, 26wt%, 27wt%, 28wt%, 29wt%, 30wt%, 31wt%, 32wt%, 33wt%, 34wt%,35wt%, 36wt%, 3wt5, 38wt%, 39wt%, 40wt%, 41wt%, 42wt%, 43wt%, 44wt%, and most preferably at least 45wt% by weight of the composition.
- a person skilled in the art may select the appropriate presentation form, and also the method for preparing it, on the basis of his general knowledge, taking into account firstly the nature of the constituents used, especially their solubility in the support, and secondly the intended use of the composition.
- compositions below are given for illustrative purposes and with no limiting nature.
- Base line time being the time point before the application of the composition of the present invention.
- 37 female subjects aged 18-45 years (both ages inclusive) were enrolled and all the 37 subjects completed the study.
- 10 self-perceived sensitive skin subjects were included.
- Visit 1- (Day 1) - Subjects were screened based on the inclusion exclusion criteria and enrolled in the study after obtaining the informed consent. Subjects were asked to report to the site without any make up/product application. Subjects washed their face with water and were acclimatized at a room temperature for 10 minutes. Baseline assessment which included Dermatologist’s visual assessment, instrument measurement (Spectrophotometer, Corneometer) and imaging (VISIA) was performed. Post baseline assessment, the test product was applied by the expert to the subjects. TO assessment (5-10 minutes post product application) was performed which included dermatologist’s visual assessment, instrument measurement (Spectrophotometer, Corneometer) and subject self-assessment. Following up assessment was performed at T8 and T12A. Post T12A assessment, subjects were asked to remove and reapply the test product. Subjects were instructed to return home and report to site after 12 hours. During this time, subjects were instructed not remove the product or wash their face.
- Baseline assessment which included Dermatologist’s visual assessment, instrument measurement (Spectropho
- Visit 3 (Day 3): Sweat room assessment Subjects were reported to the study site without any product application for sweat assessment. Subjects washed their face with water and acclimatized at a room temperature for 10. Post this, product was applied on the subject’s face and imaging was performed. Subjects sat in the hot room for 30 minutes. After 30 minutes, subjects
- Spectrophotometer- Forehead Control-Upper inner arm at the baseline were assessed At different time points Baseline, TO, T8, T12A, T12B, T14, T16, T18, T20 and T24.
- Spectrophotometer is a handheld, portable measurement instrument. The measurement is based on absorption and Reflectance of light from the surface. The instrument provides the data in Lab* colour coordinates. L* value which is responsible for luminance/ brightness.
- ITA Individual Topology Angle
- b* parameter The difference along the yellow-blue axis (b* parameter), and along the lightness-darkness axis (L* parameter) determine the intensity of skin pigmentation.
- ITA° can be expected to be a higher positive value than that of an individual with a darker skin phototype.
- ITA° is compared for all-time points, with respect to baseline. Higher value indicates whiter/lighter skin when compared to baseline.
- the Corneometer indicates the hydration level of the superficial layers of the skin (stratum corneum) via measurement of skin dielectric properties. The measurements were performed by the applying the probe to the skin surface. Upon contact, an electric field passes through the stratum corneum, and the dielectric constant is obtained
- the images taken at all-time points were aligned in the same assessment sheet and compared with the time of application.
- test product was noted to be retained for up to 24 hours.
- the composition of the present invention was altered with various combinations of silicone resins with rest of the ingredients remaining the same.
- the balloon test is qualitative test to evaluate elasticity of composition under stress
- Material Required Balloon (with Elasticity to blow 10X large to original size), Air Blower pump, Formulation/composition, thread.
- Method- A balloon was taken of the above-mentioned capacity and the product was applied- 2mg/cm 2 on balloon.
- the balloon was inflated to minimum 10X and maximum 25X of its original state (non- Inflated) using the standard formula for volume of sphere.
- the integrity of the product was checked at inflated state.
- the balloon was allowed to deflate to original state and again the integrity of the product applied on balloon was checked and the size of the area/stretching of the applied area was measured.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP22191068 | 2022-08-18 | ||
| PCT/EP2023/072243 WO2024037974A1 (en) | 2022-08-18 | 2023-08-10 | A long-wear facial composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP4572856A1 true EP4572856A1 (en) | 2025-06-25 |
Family
ID=83004656
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP23755089.2A Pending EP4572856A1 (en) | 2022-08-18 | 2023-08-10 | A long-wear facial composition |
Country Status (2)
| Country | Link |
|---|---|
| EP (1) | EP4572856A1 (en) |
| WO (1) | WO2024037974A1 (en) |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3079395B2 (en) | 1991-06-26 | 2000-08-21 | 三好化成株式会社 | Organosilicon compound-treated pigment, its production method and cosmetics |
| US5458681A (en) | 1991-06-26 | 1995-10-17 | Miyoshi Kasei Co., Ltd. | Organosilicon-treated pigment, process for production thereof, and cosmetic made therewith |
| US20060067904A1 (en) * | 2004-09-30 | 2006-03-30 | Russ Julio G | Cosmetic compositions containing amphiphilic silicone resin emulsifier |
| US20070092462A1 (en) * | 2005-10-24 | 2007-04-26 | Julio Gans Russ | Cosmetic compositions |
| CN107334685B (en) * | 2017-08-08 | 2019-11-29 | 广州蜜妆生物科技有限公司 | A kind of moisturizing, which highlights, repairs Yan Shuan |
| EP3954359A4 (en) * | 2019-04-11 | 2023-03-01 | Natura Cosméticos S.A. | TOPICAL COSMETIC COMPOSITION AND USES THEREOF |
-
2023
- 2023-08-10 EP EP23755089.2A patent/EP4572856A1/en active Pending
- 2023-08-10 WO PCT/EP2023/072243 patent/WO2024037974A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| WO2024037974A1 (en) | 2024-02-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2671245C (en) | Cosmetic composition containing novel fractal particle-based gels | |
| RU2667971C2 (en) | Cosmetic skin makeup composition | |
| JP6639052B2 (en) | Cosmetic powder for adjusting oil | |
| JP6474084B2 (en) | Finishing composition comprising silicone fine particles and non-volatile oil | |
| EP2109437B1 (en) | Cosmetic composition containing novel fractal particle based gels having improved optical properties | |
| RU2674980C1 (en) | Water or water-alcohol gel of synthetic phyllosilicates as agent increasing viscosity, producing matt effect and/or ensuring clean application | |
| US8591924B2 (en) | High-coverage and natural-looking cosmetic compositions and uses thereof | |
| US20060134035A1 (en) | Long wear topical composition having improved glossy appearance | |
| KR20160094341A (en) | UV block cosmetic composition comprising high inorganic uv absorbers | |
| JP2021501192A (en) | A composition having a satin luster effect that gives brightness, including particles of cellulose, boron nitride and a pearl brightener exhibiting satin luster. | |
| US20090185984A1 (en) | Colorants surface treated with urethanes and methods for making and using the same | |
| CN113226261A (en) | Cosmetic composition with matte effect | |
| WO2015094413A2 (en) | Styrene maleic anhydride polymers in cosmetics and personal care products | |
| JP6105300B2 (en) | Oil-in-water makeup cosmetics | |
| US9931293B2 (en) | Cosmetic compositions for minimizing skin imperfections | |
| WO2024037974A1 (en) | A long-wear facial composition | |
| JP2013209318A (en) | Oily solid cosmetic | |
| JP2003146840A (en) | Oily foundation | |
| JP6176701B2 (en) | Cosmetics | |
| JPH07258036A (en) | Solid powder cosmetic | |
| JP7752812B1 (en) | Metal oxide dispersion composition | |
| WO2024037845A1 (en) | A moisturizing composition | |
| JP2012051844A (en) | Surface-treated powder, process of producing the same and cosmetic containing the same | |
| KR102855645B1 (en) | Water-in-Oil Type Make-up Cosmetic Composition Containing Acrylate-based Copolymer and Cover Powder | |
| WO2017103052A1 (en) | Cosmetic composition based on white pigments and spherical titanium dioxide aggregates |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: UNKNOWN |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE |
|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
| 17P | Request for examination filed |
Effective date: 20241227 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC ME MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
| RAP3 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: UNILEVER IP HOLDINGS B.V. Owner name: UNILEVER GLOBAL IP LIMITED |
|
| DAV | Request for validation of the european patent (deleted) | ||
| DAX | Request for extension of the european patent (deleted) |