EP3585352A1 - Cosmetic or dermatological preparations having a content of inorganic pigments, which are coated with hydrophilic silica, and having one or more stabilizers - Google Patents
Cosmetic or dermatological preparations having a content of inorganic pigments, which are coated with hydrophilic silica, and having one or more stabilizersInfo
- Publication number
- EP3585352A1 EP3585352A1 EP18700100.3A EP18700100A EP3585352A1 EP 3585352 A1 EP3585352 A1 EP 3585352A1 EP 18700100 A EP18700100 A EP 18700100A EP 3585352 A1 EP3585352 A1 EP 3585352A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- group
- raw materials
- coated
- preparations according
- cosmetic
- 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.)
- Withdrawn
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0241—Containing particulates characterized by their shape and/or structure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/062—Oil-in-water emulsions
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/25—Silicon; Compounds 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
-
- 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
- A61K8/731—Cellulose; Quaternized cellulose derivatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/732—Starch; Amylose; Amylopectin; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/895—Polysiloxanes containing silicon bound to unsaturated aliphatic groups, e.g. vinyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/60—Particulates further characterized by their structure or composition
- A61K2800/61—Surface treated
- A61K2800/62—Coated
- A61K2800/621—Coated by inorganic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/60—Particulates further characterized by their structure or composition
- A61K2800/65—Characterized by the composition of the particulate/core
- A61K2800/651—The particulate/core comprising inorganic material
Definitions
- Cosmetic or dermatological preparations containing inorganic pigments coated with hydrophilic silica and one or more stabilizers.
- the invention relates to cosmetic or dermatological preparations containing inorganic pigments coated with hydrophilic silica and stabilizers.
- decorative cosmetics derives from the Latin “decoratio” - the highlighting of the beautiful - with the help of dyes, individual parts of the body, especially on the face, are highlighted and color inconsistencies are lessened Give appearance, refresh pale skin, compensate for color irregularities of the skin as well as emphasize eyes and lips.
- a particular embodiment is the so-called Foundation.
- Foundation is liquid or semisolid make-up that is mostly skin colored and applied to the face. They give a uniform, healthy, tinted or reddish appearance. Their color is usually obtained by a mixture of pigments from the group of inorganic white, colored and / or colored pigments.
- the prior art requires relatively large amounts of these inorganic whitening, coloring and / or colored pigments. The greater the proportion of this Pigments in the preparation, the better the skin is balanced. Redness and other visual skin irregularities are masked.
- a disadvantage of the prior art is the fact that water-based foundations can be formulated only with a relatively low pigment content, since with an increasing content of insoluble particles or pigments instabilities or rheological changes of the suspension, such as Decrease in viscosity, occur.
- the desired decorative effects can only be achieved with sufficiently high amounts of pigments.
- agents are used, for example, stimulate the activity of skin cells, but also increasingly used UV filters that block especially responsible for skin aging UVA rays. All these ingredients pose a great challenge for a pleasant sensory, as they remain as a film on the skin after evaporation of the volatile constituents of the formulation, and sensed by the consumer sensory there.
- the sensible residues are often described negatively and prevent the feeling that the product is completely "absorbed" in the skin.
- the lipids in a proportion of 0.5 to 5% based on the total weight of the preparation.
- Particularly advantageous inorganic pigments which are coated with hydrophilic silica are the so-called “Primrose” pigments from Miyoshi Kasei Inc.
- Preferred representatives of these silica-coated, hydrophilic, inorganic pigments have an average particle size of 1, 0-3.0 ⁇ m and have the following typical composition: 85.0-90.0% of inorganic pigments as core and 10.0-15.0 % Silicon dioxide (silica) as a coating.
- Typical metal oxides used in the inorganic pigments are titanium dioxide, iron oxide, chromium oxide and manganese oxide. The sub different oxidation states of the metal oxide, especially the iron oxide, are responsible for the different colors, the following classes are, which are summarized in the so-called Color Index: Cl 77499 (black), Cl 77491 (red), Cl 77492 (yellow).
- Cosmetic or dermatological preparations according to the invention preferably contain from 0.01 to 50% by weight, preferably from 0.05 to 30% by weight, particularly preferably from 0.1 to 20% by weight, of one or more of the pigments of the invention Group of inorganic whitening, coloring or colored pigments which are coated with hydrophilic silica, based on the total composition of the preparations.
- the aqueous phase of the preparations according to the invention may advantageously contain one or more polymers, which may be advantageously selected from the group, polysaccharides or their derivatives, e.g. Hyaluronic acid, xanthan gum, carrageenan, cellulose ethers, e.g.
- Hydroxypropylmethylcellulose or ethylcellulose particularly advantageously from the group of polyacrylates, preferably a polyacrylate from the group of the so-called Carbopols, for example Carbopols types 980, 981, 1382, 2984, 5984, Ultrez 10, ETD 2020, Acrylates / C 10-30 alkyl acrylates Crosspolymer, sodium acrylate copolymer, carbomer, individually or in combination.
- Carbopols for example Carbopols types 980, 981, 1382, 2984, 5984, Ultrez 10, ETD 2020, Acrylates / C 10-30 alkyl acrylates
- Crosspolymer sodium acrylate copolymer, carbomer, individually or in combination.
- Cosmetic or dermatological preparations according to the invention preferably contain 0.01-10% by weight, preferably 0.05-5% by weight, particularly preferably 0.1-2% by weight of one or more of the polymers according to the invention on the total composition of the preparations.
- Powder raw materials or fillers in the context of the present invention are particulate substances which generally do not produce a color effect in the cosmetic formulation in which they are used. Furthermore, fillers according to the invention usually have a low refractive index and, as a result, no or very little opacity.
- the prior art knows a number of powder raw materials, which are used to obtain matting effects on the skin or to absorb sebum.
- the use of powder raw materials generally also influences the dispersibility of conventional formulations on the skin and the uniformity of a possible color effect.
- the powder raw materials in the context of the present invention are advantageously selected from the group of inorganic powder raw materials, for example from the group of silicates.
- Silicates are salts and esters (silicic acid esters) of orthosilicic acid [Si (OH) 4 ] and their condensation products.
- the silicates are not only the most species-rich class of minerals, but also extremely important geologically and technically. Over 80% of the earth's crust is made up of silicates.
- Layer silicates are (ideally) silicate structures with two-dimensionally infinite layers of [Si04] 4 ⁇ tetrahedra, each tetrahedron being connected to neighboring tetrahedrons via 3 bridging oxygens.
- Chemical formulas can only be approximated for phyllosilicates because they have a large ion exchange capacity and silicon can be exchanged for aluminum and this in turn against magnesium, Fe 2+ , Fe 3+ , Zn and the like.
- the resulting possibly negative charge of the layers is usually compensated by cations, in particular by Na + and Ca 2+ in interlayer positions.
- Phyllosilicates can be obtained by reversible storage of water (in the 2- to 7-fold amount) and other substances such. As alcohols, glycols and the like swell. Their use as thickeners in cosmetic products is accordingly known per se. However, the prior art could not point the way to the present invention.
- Advantageous phyllosilicates which can be used in the context of the present invention are, for example, those whose largest expansion direction in the unmodified and unswollen state has an average length of less than 10 ⁇ m.
- the mean extents of the modified layered silicate particles used may be 1000 nm ⁇ 100 nm ⁇ 1 nm and less.
- the effective size of the modified layered silicate particles in a cosmetic or dermatological formulation of course depends on the amount of stored substances.
- Particularly advantageous (layered) silicates according to the invention are:
- Kaolin Al 2 [Si 2 O 5 ] (OH) 4
- Bentonite montmorillonite with Ca (filler earth) or Na (Wyoming bentonite) hectorite: M + o, 3 (Mg2,7Lio, 3) [Si40io (OH) 2 ], where M + is mostly Na + ,
- Mica an aluminosilicate that is easily fissile and is present in tabular crystals. Mica is transparent to translucent and has pearlescence. The most important form is muscovite: K Al 2 [AIS13O10] (OH, F) 2 . Sericite is a special form of mica that has smaller platelets than muscovite.
- silicon oxides Si0 2
- Aerosils fumed silica
- Aerosils which are highly disperse silicas with frequently irregular shape, whose specific surface area is generally very large (200-400 m 2 / g) and which can be controlled by means of the production process, are preferred according to the invention. Aerosils are also referred to as: Amorphous Silica Amorphous Silicon Oxide Hydrate Silica, Amorphous Silicic Anhydride Silicon Dioxide Silicon Dioxide.
- Silicon oxides can also be produced in a spherical form, in which case the specific surface area is smaller than in the aerosils, since the particles are larger and round.
- An example of this is the Ronaspheren (average particle diameter ⁇ 3 ⁇ ) from the company Merck.
- powder raw materials according to the invention are silicas whose free OH groups on the particle surface are (completely or partially) organically modified.
- the obtainable by the addition of dimethylsilyl groups silica dimethyl Silyiate such as Aerosil R972 (Degussa Hüls), Aerosil R974 (Degussa Hüls), CAB-O-SIL TS-610 (Cabot), CAB-O-SIL TS -720 (Cabot), Wacker HDK H15 (Wacker chemistry), Wacker HDK H18 (Wacker chemistry) and / or Wacker HDK H20 (Wacker chemistry).
- dimethylsilyl groups silica dimethyl Silyiate such as Aerosil R972 (Degussa Hüls), Aerosil R974 (Degussa Hggs), CAB-O-SIL TS-610 (Cabot), CAB-O-SIL TS -720 (Cabot), Wacker HDK H15 (Wacker chemistry), Wacker HDK H18 (Wacker chemistry) and / or Wacker HDK H20 (Wacker chemistry
- silicates obtainable by addition of trimethylsilyl groups (eg Aerosil R 812 (Degussa Hüls), CAB-O-SIL TS-530 (Cabot), Sipernat D 17 (Degussa Hüls), Wacker HDK H2000 (Wacker). Chemistry)).
- trimethylsilyl groups eg Aerosil R 812 (Degussa Hüls), CAB-O-SIL TS-530 (Cabot), Sipernat D 17 (Degussa Hüls), Wacker HDK H2000 (Wacker). Chemistry
- polymethylsilsesquioxanes obtainable by hydrolysis and condensation reactions of methyltrimethoxysilanes also have a round shape and their particle size distribution can be controlled by the production.
- Preferred polymethylsilsesquioxanes are available, for example, under the trade names Tospearl 2000 B from GE Bayer Silikones, Tospearl 145A from Toshiba, AEC Silicone Resin Spheres from A & E Connock and Wacker-Belsil PMS MK from Wacker-Chemie.
- Boron nitride is isoelectronic with carbon (i.e., graphite and diamond shapes are possible). Boron nitride is characterized by its chemical inertness.
- the powder raw materials in the context of the present invention are also advantageously selected from the group of organic powder raw materials.
- organic powder raw materials are z. B. natural polymers, such as microcrystalline.
- organic powder raw materials are also starch and starch derivatives, such as: corn starch Zea Mays (Amidon de maize MST (Wackherr), Argo Brand Com Starch
- Silicone Resins Trimethylsiloxysilicate (eg SR 1000 GE Bayer Silicones)
- silicone elastomers can be selected from the group of vinyl dimethicone crosspolymers, wherein Dow Corning's Dow Corning® EP-9801 Hydro Cosmetic Powder is to be emphasized (INCI: Dimethicone / Vinyl Dimethicone Crosspolymer (and) Butylene Glycol (and) Silica).
- lauroyl lysine which is sold by Ajinomoto under the name Amihope LL.
- Powder raw materials preferred according to the invention come from the group of inorganic or organic silicon compounds.
- the layer silicates are particularly preferred. Of these, kaolin, talc and mica are particularly preferred.
- the preparations are characterized in that they contain 0.1% by weight to 20% by weight, preferably 0.2% by weight to 15% by weight, in particular 0.5% by weight. 10% by weight, based on the total weight of the preparations, of one or more powder raw materials.
- Fats, waxes and other natural and synthetic fats preferably esters of fatty acids with lower C-number alcohols, e.g. with isopropanol, propylene glycol or glycerol, or esters of fatty alcohols with alkanoic acids of low C number or with fatty acids;
- Alcohols, diols or polyols of low C number, and their ethers preferably ethanol, isopropanol, propylene glycol, butylene glycol, methylpropanediol, glycerol, ethylene glycol, ethylene glycol monoethyl or monobutyl ether, propylene glycol monomethyl, monoethyl or monobutyl ether, diethylene glycol monomethyl or monoethyl ether and analogous products.
- the oil or lipid phase according to the invention may contain all oils, fats, waxes and / or lipids customary in cosmetic preparations.
- the lipids according to the present invention is substantially free of silicone oils according to the invention.
- a content of not more than 0.95% by weight, preferably not more than 0.5% by weight, more preferably not more than 0.1% by weight, of one or more silicone oils which are liquid at room temperature can be tolerated.
- oil components of the lipid phase of the preparations according to the invention completely or largely completely from the group of oils of synthetic and / or natural origin.
- These can then be advantageously selected from the group of esters of saturated and / or unsaturated, branched and / or unbranched alkanecarboxylic acids having a chain length of 3 to 30 carbon atoms and saturated and / or unsaturated, branched and / or unbranched alcohols having a chain length of 3 to 30 carbon atoms, from the group of esters of aromatic carboxylic acids and saturated and / or unsaturated, branched and / or unbranched alcohols having a chain length of 3 to 30 carbon atoms.
- ester oils can then advantageously be selected from the group isopropyl myristate, isopropyl palmitate, isopropyl stearate, n-decyl oleate, isooctyl stearate, isononyl stearate, isononyl isononanoate, cetearyl isononanoate, isodecyl neopentanoate, 2-ethylhexyl palmitate, 2-ethylhexyl laurate, 2-hexyldecyl stearate, coco-caprylate / caprate, Olefinoleate, oleyl erucate, erucyl oleate, erucyl erucate and synthetic, semi-synthetic and natural mixtures of such esters, eg jojoba oil.
- the lipid phase can be advantageously selected in part from the group of branched and unbranched hydrocarbons and waxes, dialkyl ethers, the group of saturated or unsaturated, branched or unbranched alcohols, and fatty acid triglycerides, namely the triglycerol esters of saturated and / or unsaturated, branched and / or unbranched alkanecarboxylic acids of a chain length of 8 to 24, in particular 12- 18 C-atoms.
- the fatty acid triglycerides can be selected, for example, advantageously from the group of synthetic, semi-synthetic and natural oils, such as Caprylic Capric triglyceride, sunflower oil, soybean oil, almond oil and the like.
- the lipids are selected from the group 2-ethylhexyl advantageous, octyldodecanol, isotridecyl isononanoate, isodecyl neopentanoate, Cocoglycerides, isoeicosane, 2-ethylhexyl xylcocoat, C 2 -i 5-alkyl benzoate, caprylic-capric acid triglyceride, dicaprylyl ether and, in particular cetearyl isononanoate.
- 2-ethylhexyl advantageous, octyldodecanol, isotridecyl isononanoate, isodecyl neopentanoate, Cocoglycerides, isoeicosane, 2-ethylhexyl xylcocoat, C 2 -i 5-alkyl benzoate, caprylic-capric acid triglyceride, di
- the proportion of the lipids of the preparations according to the invention in the range from 0.5 to 5% by weight, based on the total weight of the preparations
- hydrocarbons paraffin oil, squalane, hydrogenated polyisobutene, isohexadecan, isododecane; Ci 5 -ig alkane or polydecene advantageous to use in the context of the present invention.
- Usual colorants which are suitable for use as cosmetic or dermatological compositions in the context of the present invention are lipophilic dyes (eg Sudan Red, DB & C Red 17, DB & C Green 6, ⁇ -carotene, Sudan brown, DB & C Yellow 1 1, DB & C Violet 2, DB & C Orange 5 or Annatto), hydrophilic dyes (eg beetroot juice or methylene blue), pigments, pearlescent pigments and blends of such colorants.
- the pigments may be white or colored, goniochromatic or non-goniochromatic, inorganic and / or organic, coated or uncoated.
- inorganic pigments include titanium dioxide which is optionally surface-treated, zirconium oxide (ZrO 2), zinc oxide (ZnO), iron oxide (eg Fe 2 O 3), silicon oxide (SiO 2), manganese (eg MnO), aluminum ( Al 2 O 3), or ceria (eg, Ce 2 O 3), and iron oxide, chromium oxide, manganese of violet, ultramarine blue, chromium hydrate, and iron blue
- the pearlescent pigments may be exemplified by white pearlescent pigments such as mica coated with titanium or bismuth oxychloride, colored pearlescent pigments such as titanium mica with iron oxides, titanium mica especially iron blue or chromium oxide mica, titanium mica having an organic pigment of the type mentioned above and pearlescent pigments based on Bismuth oxychloride.
- the pigments can also be used advantageously in the form of commercially available oily or aqueous predispersions.
- dispersants and / or solubilizers can be added to these predispersions.
- the lipophilic phase e.g., lipid phase
- thickeners powder raw materials, pigments and the aqueous phase
- the powder raw materials and the silica-coated inorganic pigments are intensively dispersed in the water phase with the aid of a dissolver at 1000 rpm.
- the thickener is dispersed in the lipid phase and slowly added with vigorous stirring to the water phase.
- the suspension is then neutralized with sodium hydroxide solution to a pH of 6.8-2.7 and stirred for 5 minutes at 1000 rpm.
- “Stable” means that no or only little phase separation, no or only slight decrease in viscosity, no visually discernible inhomogeneity of the pigment distribution occurs. "Light instability” means that there is a moderate, visible phase separation, or a marked decrease in viscosity, or visually discernible inhomogeneity.
- Example recipe 1 a 1 b 2a 2b 3a 3b 4a 4b 5a 5b 6a 6b ren /% by weight
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102017203113.1A DE102017203113A1 (en) | 2017-02-27 | 2017-02-27 | Cosmetic or dermatological preparations containing inorganic pigments coated with hydrophilic silica and one or more stabilizers |
PCT/EP2018/050267 WO2018153555A1 (en) | 2017-02-27 | 2018-01-05 | Cosmetic or dermatological preparations having a content of inorganic pigments, which are coated with hydrophilic silica, and having one or more stabilizers |
Publications (1)
Publication Number | Publication Date |
---|---|
EP3585352A1 true EP3585352A1 (en) | 2020-01-01 |
Family
ID=60937770
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP18700100.3A Withdrawn EP3585352A1 (en) | 2017-02-27 | 2018-01-05 | Cosmetic or dermatological preparations having a content of inorganic pigments, which are coated with hydrophilic silica, and having one or more stabilizers |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP3585352A1 (en) |
DE (1) | DE102017203113A1 (en) |
WO (1) | WO2018153555A1 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112569127A (en) * | 2020-12-30 | 2021-03-30 | 广州澳希亚实业有限公司 | Liquid oily composition and preparation method and application thereof |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4119712A (en) | 1977-07-25 | 1978-10-10 | Revlon, Inc. | Makeup foundations |
DE19834821A1 (en) * | 1998-08-01 | 2000-02-03 | Beiersdorf Ag | Emulsifier-free finely dispersed systems of the oil-in-water and water-in-oil type |
DE19834820A1 (en) * | 1998-08-01 | 2000-02-03 | Beiersdorf Ag | Emulsifier-free finely dispersed systems of the oil-in-water and water-in-oil type |
EP1250915A1 (en) * | 2001-04-19 | 2002-10-23 | Beiersdorf Aktiengesellschaft | Cosmetic and dermatologic compositions comprising high electrolyt contents |
DE10355711A1 (en) * | 2003-11-26 | 2005-06-16 | Beiersdorf Ag | Cosmetic and dermatological emulsions containing creatine and / or creatinine and electrolyte concentrations, an ionic strength of at least 50 mmol / l |
DE102004005366A1 (en) | 2004-02-03 | 2005-08-18 | Eckart Gmbh & Co.Kg | Cosmetic preparation containing a metal pigment |
US7476395B2 (en) * | 2006-04-11 | 2009-01-13 | Conopco, Inc. | Cosmetic composition with soft focus properties |
DE102010049375A1 (en) | 2010-10-26 | 2012-04-26 | Merck Patent Gmbh | pigments |
DE102011055072A1 (en) | 2011-11-04 | 2013-05-08 | Eckart Gmbh | Coated, wet-chemically oxidized aluminum effect pigments, process for their preparation, coating compositions and coated articles |
-
2017
- 2017-02-27 DE DE102017203113.1A patent/DE102017203113A1/en not_active Withdrawn
-
2018
- 2018-01-05 WO PCT/EP2018/050267 patent/WO2018153555A1/en active Application Filing
- 2018-01-05 EP EP18700100.3A patent/EP3585352A1/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
WO2018153555A1 (en) | 2018-08-30 |
DE102017203113A1 (en) | 2018-08-30 |
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