FR2792328A1 - Oily composition for use in cosmetic formulations comprises paraffinic hydrocarbons such as isohexadecane and a composition rich in lipids of vegetable origin - Google Patents
Oily composition for use in cosmetic formulations comprises paraffinic hydrocarbons such as isohexadecane and a composition rich in lipids of vegetable origin Download PDFInfo
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- FR2792328A1 FR2792328A1 FR9904920A FR9904920A FR2792328A1 FR 2792328 A1 FR2792328 A1 FR 2792328A1 FR 9904920 A FR9904920 A FR 9904920A FR 9904920 A FR9904920 A FR 9904920A FR 2792328 A1 FR2792328 A1 FR 2792328A1
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B7/00—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils
- C11B7/0008—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils by differences of solubilities, e.g. by extraction, by separation from a solution by means of anti-solvents
- C11B7/0025—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils by differences of solubilities, e.g. by extraction, by separation from a solution by means of anti-solvents in solvents containing oxygen in their molecule
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- 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
- A61K8/31—Hydrocarbons
-
- 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
- A61K8/55—Phosphorus compounds
- A61K8/553—Phospholipids, e.g. lecithin
-
- 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
- A61K8/68—Sphingolipids, e.g. ceramides, cerebrosides, gangliosides
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- 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
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
- A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
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- 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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/14—Preparations for removing make-up
-
- 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
-
- 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
- A61Q19/10—Washing or bathing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B1/00—Production of fats or fatty oils from raw materials
- C11B1/10—Production of fats or fatty oils from raw materials by extracting
-
- 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
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
- A61Q1/06—Lipsticks
-
- 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
- A61Q1/10—Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Molecular Biology (AREA)
- Dermatology (AREA)
- Biophysics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Cosmetics (AREA)
Abstract
Description
MATIERE HUILEUSE COMPRENANT DES HYDROCARBURESOILY MATERIAL COMPRISING HYDROCARBONS
PARAFFINIQUES ET UN COMPOSE RICHE EN LIPIDES D'ORIGINE PARAFFINICS AND AN ORIGINAL FAT RICH COMPOUND
VEGÉTALE, SA PRÉPARATION ET LES COMPOSITIONS LA CONTENANT. VEGETABLE, ITS PREPARATION AND THE COMPOSITIONS CONTAINING IT.
La présente invention concerne une matière huileuse utile pour la préparation de compositions cosmétiques et dermatologiques présentant des propriétés nourrissantes et hydratantes remarquables, ainsi que lesdites compositions cosmétiques et dermatologiques, notamment des shampooings, savons, gels, lait et crème ou The present invention relates to an oily material useful for the preparation of cosmetic and dermatological compositions having remarkable nourishing and moisturizing properties, as well as said cosmetic and dermatological compositions, in particular shampoos, soaps, gels, milk and cream or
encore des produits de maquillage ou de démaquillage. still make-up or make-up removal products.
Les travaux de recherche réalisés par la demanderesse sur l'extraction des composés, notamment de nature lipidique, contenus dans les végétaux et plus particulièrement les céréales et farine de céréales comme le blé, lui ont permis d'obtenir des composés riches en lipides d'origine végétale susceptibles d'entrer dans la composition de matière huileuse utile pour la préparation de produits The research carried out by the applicant on the extraction of compounds, in particular of lipidic nature, contained in plants and more particularly cereals and cereal flour such as wheat, have enabled it to obtain compounds rich in lipids from vegetable origin likely to enter into the composition of oily matter useful for the preparation of products
cosmétiques et dermatologiques.cosmetic and dermatological.
En conséquence, la présente invention se rapporte à une matière huileuse comprenant des hydrocarbures parrafiniques, tels que notamment de l'isohexadécane et un Consequently, the present invention relates to an oily material comprising parrafinic hydrocarbons, such as in particular isohexadecane and a
composé riche en lipides d'origine végétale. compound rich in lipids of plant origin.
Le composé riche en lipides d'origine végétale, aussi désigné ci- après LIPOWHEAT, entrant dans la composition de la matière huileuse de l'invention, comprend plus de 50 % et avantageusement plus de 80% en poids de lipides. Ce composé présente une composition remarquable en lipides polaires. Il se présente sous la forme d'une poudre fine grasse ou de paillettes légèrement jaunes, sans saveur, à odeur caractéristique. Ce composé riche en lipides d'origine végétale comprend de l'ordre de 50 à 65 % de glycolipides y compris les glycosylcéramides. Il comprend de à 12 % et de préférence de 8 à 10 % de céramides y compris les glycosylcéramides. Ce Composé riche en lipides d'origine végétale comprend avantageusement de l'ordre de 20 à 40 % et The compound rich in lipids of plant origin, also designated below LIPOWHEAT, used in the composition of the oily material of the invention, comprises more than 50% and advantageously more than 80% by weight of lipids. This compound has a remarkable composition of polar lipids. It comes in the form of a fine oily powder or slightly yellow flakes, without flavor, with a characteristic odor. This compound rich in lipids of vegetable origin comprises of the order of 50 to 65% of glycolipids including glycosylceramides. It comprises from to 12% and preferably from 8 to 10% of ceramides including the glycosylceramides. This compound rich in lipids of vegetable origin advantageously comprises of the order of 20 to 40% and
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à 40 % et de préférence de l'ordre de 30 à 35 % de phospholipides. Ce composé présente l'intérêt de comprendre moins de 1% et même aucun lipide neutre. Un exemple préféré de composition en lipides d'un tel composé est la suivante: - Lipides neutres essentiellement des triglycérides < 1 % Phospholipides: 30 à 35 % - Glycolipides: 50 à 55 % to 40% and preferably of the order of 30 to 35% of phospholipids. This compound has the advantage of comprising less than 1% and even no neutral lipid. A preferred example of lipid composition of such a compound is as follows: - Neutral lipids essentially triglycerides <1% Phospholipids: 30 to 35% - Glycolipids: 50 to 55%
- Céramides et glycosylcéramides 8 à 10 %. - Ceramides and glycosylceramides 8 to 10%.
La matière huileuse selon l'invention comprend de préférence de 1 à 10 % et avantageusement de 2 à 5% d'au moins un composé riche en lipides d'origine végétale défini précédemment. La matière huileuse est préparée en dispersant The oily material according to the invention preferably comprises from 1 to 10% and advantageously from 2 to 5% of at least one compound rich in lipids of plant origin defined above. The oily material is prepared by dispersing
le LIPOWHEAT dans les hydrocarbures parrafiniques. LIPOWHEAT in parrafinic hydrocarbons.
La matière huileuse selon l'invention constitue une huile enrichie en lipide polaire utile pour la The oily material according to the invention constitutes an oil enriched in polar lipid useful for the
préparation de compositions cosmétiques liquides, semi- preparation of liquid, semi-cosmetic compositions
liquide ou solide, comme des produits moussants, des émulsions, des produits de maquillage ou de démaquillage. En effet, la présence d'un composé riche en lipides d'origine végétale dans la métière huileuse de l'invention confère à ces compositions des capacités d'hydratation de la peau remarquables. L'invention a donc pour objet de telles compositions comprenant un ou plusieurs agents cosmétologiquement, dermatologiquement ou pharmaceutiquement liquid or solid, such as foaming products, emulsions, make-up or make-up removing products. Indeed, the presence of a compound rich in lipids of vegetable origin in the oily substance of the invention gives these compositions remarkable hydration capacities of the skin. The subject of the invention is therefore such compositions comprising one or more agents cosmetologically, dermatologically or pharmaceutically
actifs dans un ou plusieurs véhicules acceptables. active in one or more acceptable vehicles.
L'invention concerne par exemple des shampooings, des gels douches et savon liquide comprenant la matière huileuse de l'invention. La présence de céramides et de glycosylcéramides dans ces shampooings permet de donner aux cheveux la brillance recherchée et procure un effet gainant, tout en nourrissant le cheveu. Les gels et savons liquides présentent des propriétés hydratantes et The invention relates for example to shampoos, shower gels and liquid soap comprising the oily material of the invention. The presence of ceramides and glycosylceramides in these shampoos makes it possible to give the hair the desired shine and provides a sheathing effect, while nourishing the hair. Liquid gels and soaps have moisturizing and
nourrissantes pour la peau.nourishing for the skin.
L'invention concerne donc tout particulièrement des compositions capillaires, comme des lotions, gels, émulsions, comportant une phase huileuse constituée de la The invention therefore relates very particularly to hair compositions, such as lotions, gels, emulsions, comprising an oily phase consisting of
matière huileuse de l'invention.oily material of the invention.
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L'invention concerne bien entendu les émulsions comportant une phase huile comprenant la matière huileuse de l'invention. Il s'agit par exemple de crèmes et laits hydratants, de crèmes et laits solaires qui présentent des propriétés anti-radicallaires renforcées du fait du composé The invention naturally relates to emulsions comprising an oil phase comprising the oily material of the invention. These are, for example, moisturizing creams and milks, sun creams and milks which have reinforced anti-radicallary properties due to the compound
riche en lipides polaires présent dans la matière huileuse. rich in polar lipids present in oily matter.
L'invention concerne encore des produits de maquillage comme des rouges à lèvres, du mascara, des fonds The invention also relates to makeup products such as lipsticks, mascara, funds
de teint.complexion.
D'autres avantages et caractéristiques de l'invention apparaîtront des exemples qui suivent qui concernent la préparation du composé riche en lipide d'origine végétale entrant dans la composition de l'agent émulsifiant et la préparation d'une matière huileuse selon l'invention. 1) Préparation du composé riche en lipide d'origine végétale entrant dans la composition de l'agent Other advantages and characteristics of the invention will appear from the examples which follow which relate to the preparation of the lipid-rich compound of vegetable origin used in the composition of the emulsifying agent and the preparation of an oily material according to the invention. 1) Preparation of the lipid-rich compound of plant origin used in the composition of the agent
émulsifiant.emulsifier.
Un procédé de préparation d'un composé riche en lipides d'origine végétale comprend les étapes suivantes: a) Extraction des lipides totaux: On introduit sous forte agitation un composé végétal tel que de la farine de céréales ou un produit issu de la transformation des céréales, comme du gluten, dans un solvant ou un mélange de solvants polaires, dans un rapport de 1 à 10 et de préférence de 1 à 5, à une température située entre 20 et 60 C et de préférence entre 20 et 40 C, puis l'on poursuit l'agitation pendant plusieurs heures et l'on sépare un gâteau de filtration délipidé et un filtrat riche en lipides A process for the preparation of a compound rich in lipids of vegetable origin comprises the following stages: a) Extraction of total lipids: A vegetable compound such as cereal flour or a product resulting from the transformation of cereals, such as gluten, in a solvent or a mixture of polar solvents, in a ratio of 1 to 10 and preferably from 1 to 5, at a temperature between 20 and 60 C and preferably between 20 and 40 C, then stirring is continued for several hours and a delipidated filter cake and a lipid-rich filtrate are separated
polaires et apolaires par toute méthode appropriée. polar and apolar by any suitable method.
b) Concentration: On concentre sous vide le filtrat obtenu à l'étape (a) par exemple dans un appareil de type alambic, pour obtenir une huile brune orangée homogène, puis l'on déshydrate et l'on filtre cette huile pour obtenir la fraction lipidique totale qui se présente sous la forme d'un liquide parfaitement limpide et stable dont la b) Concentration: The filtrate obtained in step (a) is concentrated under vacuum, for example in a still type device, to obtain a homogeneous orange-brown oil, then this oil is dried and filtered to obtain the total lipid fraction which is in the form of a perfectly clear and stable liquid, the
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composition en lipides neutres et lipides polaires est composition of neutral lipids and polar lipids is
parfaitement constante et reproductible. perfectly constant and reproducible.
b') récupération: on récupère le gâteau de céréales délipidé obtenue à l'étape (a) par tout moyen approprié. c) Extraction des lipides polaires: On traite la fraction lipidique totale obtenue à l'étape (b) par un solvant organique de façon à séparer les lipides polaires qui sont insolubles et précipitent de la fraction apolaire qui est solubilisée dans le solvant organique, puis l'on récupère le précipité de lipides polaires par tout moyen de b ') recovery: the defatted cereal cake obtained in step (a) is recovered by any suitable means. c) Extraction of the polar lipids: The total lipid fraction obtained in step (b) is treated with an organic solvent so as to separate the polar lipids which are insoluble and precipitate from the non-polar fraction which is dissolved in the organic solvent, then the polar lipid precipitate is recovered by any means of
séparation solide liquide adapté.suitable solid liquid separation.
Le procédé peut aussi comprendre après l'étape The process can also include after step
(c) une étape (d) d'extraction des lipides neutres. (c) a step (d) of extraction of the neutral lipids.
L'origine de la farine de céréales ou du produit issu de la transformation de céréales, comme du gluten, utilisé à l'étape (a) est choisie parmi le blé, le gluten de The origin of the cereal flour or of the product resulting from the transformation of cereals, such as gluten, used in step (a) is chosen from wheat, gluten from
blé, le riz, le millet, l'avoine, l'orge, le sorgho, etc.... wheat, rice, millet, oats, barley, sorghum, etc.
Parmi ces céréales on préfère tout particulièrement le blé dont la teneur en lipides totaux est supérieur à 5%. De préférence, la farine de céréales ou le produit issu de la transformation de céréales utilisé à l'étape (a) provient du blé et est constitué en majorité par les protéines de Among these cereals, wheat is particularly preferred, the total lipid content of which is greater than 5%. Preferably, the cereal flour or the product resulting from the transformation of cereals used in step (a) comes from wheat and consists mainly of protein.
réserve du blé (le gluten).wheat reserve (gluten).
Le solvant polaire de l'étape (a) est par exemple le méthanol, l'éthanol, etc.... ou un mélange de The polar solvent of step (a) is for example methanol, ethanol, etc., or a mixture of
ceux-ci. Parmi ceux-ci, on préfère l'éthanol absolu. these. Of these, absolute ethanol is preferred.
Une méthode appropriée pour séparer, à l'étape (a), le gâteau de filtration délipidé et un filtrat riche en lipides polaires et apolaires est par exemple une A suitable method for separating, in step (a), the defatted filter cake and a filtrate rich in polar and non-polar lipids is for example a
filtration, une centrifugation ou un essorage. filtration, centrifugation or spinning.
Il convient de remarquer que l'extraction à l'alcool réalisé à l'étape (a) permet de solubiliser les triglycérides, les phospholipides, les glycolipides, les It should be noted that the alcohol extraction carried out in step (a) makes it possible to dissolve the triglycerides, the phospholipids, the glycolipids, the
céramides et glycosylcéramides.ceramides and glycosylceramides.
L'évaporation du solvant ou du mélange de solvant polaire, comme l'éthanol, de l'étape (b) est avantageusement réalisée au moyen d'un réacteur de type The evaporation of the solvent or of the polar solvent mixture, such as ethanol, from step (b) is advantageously carried out by means of a type reactor.
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alambic équipé d'une double paroi dans laquelle circule une huile thermique dont la température est ajustée en fonction des besoins du procédé et du niveau de vide de l'installation. Il est ainsi possible de récupérer au fond du réacteur la fraction lipidique totale qui se présente sous la forme d'un résidu liquide parfaitement homogène still equipped with a double wall in which circulates a thermal oil whose temperature is adjusted according to the needs of the process and the vacuum level of the installation. It is thus possible to recover from the bottom of the reactor the total lipid fraction which is in the form of a perfectly homogeneous liquid residue.
contenant environ 3 % de céramides et glycosylcéramides. containing approximately 3% of ceramides and glycosylceramides.
L'extraction des lipides polaires de l'étape (c) est réalisée à l'aide d'un solvant organique choisi parmi The extraction of the polar lipids of step (c) is carried out using an organic solvent chosen from
l'acétone, l'éther, le benzène,, ou d'un mélange de ceux- acetone, ether, benzene, or a mixture of these
ci. Parmi ceux-ci on préfère plus particulièrement l'acétone. Afin d'obtenir un concentré de lipides polaires de caractéristiques constantes et reproductibles, le traitement de l'étape (c) consiste à réaliser de 1 à 5 et de préférence 3 extractions successives avec un solvant organique dans un rapport en solvant organique par rapport à la fraction lipidique totale compris entre 1 et 10 v/v et de préférence entre 1 et 8 v/v, et dans les conditions de température et d'agitation préférées suivantes: un température inférieure à 20 C et de préférence inférieure à 15 C, et l'on préfère tout particulièrement une température comprise entre 5 et 10 C; - un mode agitation adapté à un travail de dispersion d'un liquide dans un autre liquide lors de la première extraction, et à un travail de cisaillement de. la pâte lipidique lors des opérations suivantes si l'on effectue plus d'une extraction, le mode d'agitation devant cependant éviter la dissolution d'oxygène de l'air dans le mélange; - une durée d'agitation comprise entre 15 et 45 this. Among these, acetone is more particularly preferred. In order to obtain a polar lipid concentrate with constant and reproducible characteristics, the treatment in step (c) consists in carrying out from 1 to 5 and preferably 3 successive extractions with an organic solvent in an organic solvent ratio relative to the total lipid fraction between 1 and 10 v / v and preferably between 1 and 8 v / v, and under the following preferred temperature and stirring conditions: a temperature below 20 C and preferably below 15 C, and very particularly preferred is a temperature between 5 and 10 C; - A stirring mode suitable for a job of dispersing a liquid in another liquid during the first extraction, and a shear work of. the lipid paste during the following operations if more than one extraction is carried out, the stirring mode however having to avoid the dissolution of oxygen from the air in the mixture; - a duration of agitation between 15 and 45
minutes et de préférence de l'ordre de 20 à 30 minutes. minutes and preferably of the order of 20 to 30 minutes.
- le solvant organique utilisé doit avoir une - the organic solvent used must have a
teneur en eau maximale de 0,3 %.maximum water content of 0.3%.
Le précipité de lipides polaires obtenu à l'étape (c) est récupéré par tout moyen de séparation solide liquide adapté, comme par exemple une filtration frontale sous vide ou un essorage centrifuge sur toile filtrante 5-10 p entre 1500 et 2500 t/mn. On préfère plus particulièrement The polar lipid precipitate obtained in step (c) is recovered by any suitable liquid solid separation means, such as for example front vacuum filtration or centrifugal spinning on a 5-10 p filter cloth between 1500 and 2500 rpm . We particularly prefer
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cette dernière technique car elle améliore la siccité en solvant du gâteau récupéré et est donc plus adaptée à une the latter technique because it improves the solvent dryness of the recovered cake and is therefore more suitable for
mise en oeuvre industrielle.industrial implementation.
Avantageusement, la pâte riche en lipides polaires récupérée à l'issue de l'étape (c) est séchée sous vide à une température de l'ordre de 35 C ou lyophilisée à des températures de congélation de l'ordre de -45 C, de sublimation de l'ordre de -30 C, et de désorption de l'ordre Advantageously, the paste rich in polar lipids recovered at the end of step (c) is dried under vacuum at a temperature of the order of 35 C or freeze-dried at freezing temperatures of the order of -45 C, sublimation of the order of -30 C, and desorption of the order
de 40 C, ou encore atomisée.of 40 C, or even atomized.
Exemple 2: Préparation d'une matière huileuse Example 2: Preparation of an oily material
selon l'invention.according to the invention.
La matière huileuse selon l'invention est préparée en dispersant le LIPOWHEAT dans i'ARLAMOL HD The oily material according to the invention is prepared by dispersing LIPOWHEAT in i'ARLAMOL HD
commercialisé par la Société ICI (Nom INCI: Isohexadecane). marketed by the company ICI (INCI name: Isohexadecane).
Le LIPOWHEAT (2 %) est ajouté à froid dans i'ARLAMOL HD, puis on mélange sous une agitation modérée, de l'ordre de 300 rpm, à une température d'environ 45 à 50 C pendant 10 à The LIPOWHEAT (2%) is added cold to i'ARLAMOL HD, then mixed with moderate stirring, of the order of 300 rpm, at a temperature of approximately 45 to 50 C for 10 to
15 minutes.15 minutes.
Claims (6)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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FR9904920A FR2792328B1 (en) | 1999-04-19 | 1999-04-19 | OILY MATERIAL COMPRISING PARAFFINIC HYDROCARBONS AND PLANT-RICH LIPID-RICH COMPOUND, PREPARATION THEREOF AND COMPOSITIONS CONTAINING THE SAME |
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FR9904920A FR2792328B1 (en) | 1999-04-19 | 1999-04-19 | OILY MATERIAL COMPRISING PARAFFINIC HYDROCARBONS AND PLANT-RICH LIPID-RICH COMPOUND, PREPARATION THEREOF AND COMPOSITIONS CONTAINING THE SAME |
Publications (2)
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FR2792328A1 true FR2792328A1 (en) | 2000-10-20 |
FR2792328B1 FR2792328B1 (en) | 2005-04-15 |
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FR9904920A Expired - Fee Related FR2792328B1 (en) | 1999-04-19 | 1999-04-19 | OILY MATERIAL COMPRISING PARAFFINIC HYDROCARBONS AND PLANT-RICH LIPID-RICH COMPOUND, PREPARATION THEREOF AND COMPOSITIONS CONTAINING THE SAME |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006120003A1 (en) * | 2005-05-12 | 2006-11-16 | Basf Aktiengesellschaft | Isoalkane mixture, its preparation and use |
US8821842B2 (en) | 2005-05-12 | 2014-09-02 | Basf Se | Isoalkane mixture, its preparation and use |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1992021321A1 (en) * | 1991-05-27 | 1992-12-10 | Laboratoires Inocosm | Method for separating a vegetable compound |
WO1995025503A1 (en) * | 1994-03-18 | 1995-09-28 | The Procter & Gamble Company | Powder cosmetic compositions |
WO1996037192A1 (en) * | 1995-05-26 | 1996-11-28 | Vesifact Ag | Pharmaceutical and cosmetic compositions containing sphingo- and glycolipids |
FR2735361A1 (en) * | 1995-06-13 | 1996-12-20 | Oreal | Dispersion used to protect skin or hair esp. against UV light |
JPH1192781A (en) * | 1997-09-18 | 1999-04-06 | Nippon Flour Mills Co Ltd | Method for obtaining glycolipid from grain, material for cosmetic containing the same, and cosmetic and food |
-
1999
- 1999-04-19 FR FR9904920A patent/FR2792328B1/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1992021321A1 (en) * | 1991-05-27 | 1992-12-10 | Laboratoires Inocosm | Method for separating a vegetable compound |
WO1995025503A1 (en) * | 1994-03-18 | 1995-09-28 | The Procter & Gamble Company | Powder cosmetic compositions |
WO1996037192A1 (en) * | 1995-05-26 | 1996-11-28 | Vesifact Ag | Pharmaceutical and cosmetic compositions containing sphingo- and glycolipids |
FR2735361A1 (en) * | 1995-06-13 | 1996-12-20 | Oreal | Dispersion used to protect skin or hair esp. against UV light |
JPH1192781A (en) * | 1997-09-18 | 1999-04-06 | Nippon Flour Mills Co Ltd | Method for obtaining glycolipid from grain, material for cosmetic containing the same, and cosmetic and food |
Non-Patent Citations (1)
Title |
---|
PATENT ABSTRACTS OF JAPAN vol. 1999, no. 09 30 July 1999 (1999-07-30) * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006120003A1 (en) * | 2005-05-12 | 2006-11-16 | Basf Aktiengesellschaft | Isoalkane mixture, its preparation and use |
US8821842B2 (en) | 2005-05-12 | 2014-09-02 | Basf Se | Isoalkane mixture, its preparation and use |
Also Published As
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FR2792328B1 (en) | 2005-04-15 |
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