FR2736827A1 - Oil extracted from plant of genus Calophyllum - is used as cosmetic, esp. as filter against wide UV band - Google Patents
Oil extracted from plant of genus Calophyllum - is used as cosmetic, esp. as filter against wide UV band Download PDFInfo
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- FR2736827A1 FR2736827A1 FR9509123A FR9509123A FR2736827A1 FR 2736827 A1 FR2736827 A1 FR 2736827A1 FR 9509123 A FR9509123 A FR 9509123A FR 9509123 A FR9509123 A FR 9509123A FR 2736827 A1 FR2736827 A1 FR 2736827A1
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- 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
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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
- A61Q19/00—Preparations for care of the skin
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Abstract
Description
L'invention concerne une huile cosmétique d'origine naturelle, son utilisation en tant que produit cosmétique, ainsi que des compositions cosmétiques contenant une telle huile. The invention relates to a cosmetic oil of natural origin, its use as a cosmetic product, as well as cosmetic compositions containing such an oil.
Les radiations lumineuses de longueur d'onde comprise entre 280 nm et 400 nm permettent le brunissement de l'épiderme humain. Mais ces radiations, qu'elles soient d'origine solaire ou artificielle, peuvent également exercer un effet néfaste entraînant par exemple une altération de l'épiderme, notamment dans le cas de peaux sensibles ou d'exposition prolongée aux rayonnements. The luminous radiations of wavelength between 280 nm and 400 nm allow the browning of the human epidermis. However, these radiations, whether of solar or artificial origin, can also exert a harmful effect resulting for example an alteration of the epidermis, in particular in the case of sensitive skins or prolonged exposure to the radiations.
Ainsi, les rayonnements de longueur d'onde comprise entre 320 nm et 400 nm, connus sous le nom de UV-A, peuvent provoquer une perte d'élasticité de la peau et l'apparition de rides conduisant à un vieillissement prématuré de celle-ci. Les UV-A peuvent également être à l'origine de réactions phototoxiques ou photoallergiques, et leur rôle dans l'apparition de cancers cutanés a été reconnu. Thus, wavelength radiation between 320 nm and 400 nm, known as UV-A, can cause a loss of elasticity of the skin and the appearance of wrinkles leading to premature aging of the skin. this. UV-A can also cause phototoxic or photoallergic reactions, and their role in the development of skin cancers has been recognized.
En outre, les rayonnements de longueur d'onde comprise entre 280 nm et 320 nm, connus sous le nom d'UV-B, peuvent provoquer des érythèmes et des brûlures cutanées. In addition, wavelength radiation between 280 nm and 320 nm, known as UV-B, can cause erythema and skin burns.
Aussi, la nécessité de protéger l'épiderme contre chacun de ces types de rayonnements s'est faite sentir. Elle a conduit les fabricants de produits cosmétiques de protection solaire à utiliser principalement des filtres spécifiques, soit pour les UV
A, soit pour les UV-B.Also, the need to protect the epidermis against each of these types of radiation has been felt. It has led manufacturers of sunscreen cosmetics to primarily use specific filters, either for UV
A, for UV-B.
En outre, on a également cherché à utiliser des filtres à larges bandes, absorbant à la fois les rayonnements UV-B et UV -A. Actuellement, il s'agit généralement de produits obtenus par synthèse. In addition, it has also been sought to use broadband filters, absorbing both UV-B and UV-A radiation. Currently, these are generally synthetic products.
Un des buts de l'invention est de proposer une huile cosmétique d'origine naturelle qui soit facile et peu onéreuse à extraire, et qui présente des propriétés de protection contre les rayonnements solaires au moins équivalentes à celles des produits à protection large existants. One of the aims of the invention is to provide a cosmetic oil of natural origin which is easy and inexpensive to extract, and which has protection properties against solar radiation at least equivalent to those of existing wide protection products.
A cet effet, I'invention a pour objet une huile extraite d'une plante du genre Callophyllum pour son utilisation en tant que produit cosmétique. For this purpose, the subject of the invention is an oil extracted from a plant of the genus Callophyllum for its use as a cosmetic product.
Plus particulièrement, L'huile extraite des plantes du genre
Calophyllum peut être utilisée en tant que produit filtrant à large bande contre les rayonnements ultraviolets.More particularly, oil extracted from plants of the genus
Calophyllum can be used as a broadband filtering product against ultraviolet radiation.
La plante du genre Calophyllum est avantageusement choisie parmi les espèces suivantes . eputamen ; . inophyllum ; parviflorum . soulattri ; tacamahaca . spectabile ; . recedens ; . comorense ;
Chapelieri
Drouhardi . laxiflorum.The plant of the genus Calophyllum is advantageously chosen from the following species. eputamen; . inophyllum; parviflorum. soulattri; tacamahaca. spectabile; . recedens; . comorense;
chapelieri
Drouhardi. laxiflorum.
L'huile peut être choisie de telle sorte qu'elle contienne une fraction de 0,5 à 2 % environ d'un ou plusieurs composés insaponifiables parmi les composés suivants hydrocarbures alcools gras stérols et méthyl stérols xanthones dérivés coumariniques composés triterpéniques. The oil may be selected such that it contains a fraction of about 0.5 to about 2% of one or more unsaponifiable compounds among the following compounds: hydrocarbon fatty alcohols sterols and methyl sterols xanthones derivatives coumarinic triterpene compounds.
L'invention concerne aussi l'utilisation d'une huile extraite des plantes du genre Calophyllum en tant que produit cosmétique, ainsi que son utilisation en tant que produit filtrant à large bande contre les rayonnements ultraviolets. The invention also relates to the use of an oil extracted from plants of the genus Calophyllum as a cosmetic product, as well as its use as a broad-band filtering product against ultraviolet radiation.
L'invention concerne également une composition cosmétique comprenant une phase grasse contenant une huile extraite des plantes du genre Callophyllum. The invention also relates to a cosmetic composition comprising a fatty phase containing an oil extracted from plants of the genus Callophyllum.
II pourra s'agir d'une huile solaire, comprenant - huile de Calophyllum 25,0 g - huile de tournesol 2,0 g - beurre de karité 1,0 g - acétate de vitamine E 0,3 g - imidazolidinyl urée 0,2 g - parfum qs - alcool éthylique absolu qsp 100,0 g
En variante, il pourra s'agir d'une émulsion solaire sous forme de gel-crème, comprenant - huile de Calophyllum 15,0 g - polyglycéryl méthacrylate/propylène glycol 15,0 9 - méthyl paraben 0,3 g - glycérine 5,0 g - imidazolidinyl urée 0,2 g - conservateurs qs - parfum qs - eau qsp 100,0 g
L'invention concerne également l'utilisation d'une telle composition en tant que produit cosmétique, ainsi que son utilisation en tant que produit filtrant à large bande des rayonnements ultraviolets. It may be a solar oil, comprising - Calophyllum oil 25.0 g - Sunflower oil 2.0 g - Shea butter 1.0 g - Vitamin E acetate 0.3 g - Imidazolidinyl urea 0, 2 g - perfume qs - absolute ethyl alcohol qs 100.0 g
Alternatively, it may be a solar gel-cream emulsion comprising - Calophyllum oil 15.0 g - polyglyceryl methacrylate / propylene glycol 15.0 9 - methyl paraben 0.3 g - glycerin 5, 0 g - imidazolidinyl urea 0.2 g - preservatives qs - perfume qs - water qs 100.0 g
The invention also relates to the use of such a composition as a cosmetic product, as well as its use as a broadband filter product of ultraviolet radiation.
L'invention concerne aussi une huile extraite des plantes du genre Calophyllum pour la préparation d'une composition cosmétique, ainsi que son utilisation pour la préparation d'une composition filtrante à large bande contre les rayonnements ultraviolets. The invention also relates to an oil extracted from plants of the genus Calophyllum for the preparation of a cosmetic composition, as well as its use for the preparation of a broadband filter composition against ultraviolet radiation.
L'huile extraite des plantes du genre Calophyllum est connue comme agent anti-inflammatoire, en effet, elle a la propriété de réduire la perméabilité des capillaires sanguins (voir R.C. Saxena et al., Effect of Calophyllolide, a non steroidal anti-inflammatory agent, on capillary permeability, Planta Medica, 1982, 44, 246248). The oil extracted from plants of the genus Calophyllum is known as an anti-inflammatory agent, indeed, it has the property of reducing the permeability of blood capillaries (see RC Saxena et al., Effect of Calophyllolide, a non-steroidal anti-inflammatory agent , capillary permeability, Planta Medica, 1982, 44, 246248).
La demanderesse a découvert que les huiles naturelles extraites des plantes appartenant au genre Calophyllum présentent des caractéristiques filtrantes prononcées, et sont susceptibles de jouer un rôle de filtre à large bande. The Applicant has discovered that the natural oils extracted from plants belonging to the genus Calophyllum exhibit pronounced filtering characteristics and are capable of acting as a broadband filter.
Le genre Callophyllum, appartenant à la famille des guttifères, comprend environ 200 espèces. Leur aire d'implantation comprend l'Afrique de l'Est et Madagascar, la Chine du Sud, la Malaisie, I'Australie, la Nouvelle Calédonie, les îles du
Pacifique Ouest, ainsi qu'une zone s'étendant de l'Amérique
Centrale et des Antilles à l'Amérique du Sud.The genus Callophyllum, belonging to the family of guttifers, comprises about 200 species. Their area of settlement includes East Africa and Madagascar, South China, Malaysia, Australia, New Caledonia, the islands of
West Pacific, as well as an area stretching from America
Central and West Indies to South America.
II s'agit d'arbres élevés à suc blanchâtre donnant une gomme ou résine de même couleur. Ces arbres fournissent une drupe généralement globuleuse ou ovoïde, à péricarpe mince ou fibreux et relativement épais. La graine est ovoïde ou globuleuse ascendante, à testa mince, épais ou spongieux, dépourvue d'albumen, mais avec un embryon principalement constitué de deux gros cotylédons distincts, libres ou plus ou moins soudés. They are tall trees with whitish juice giving a gum or resin of the same color. These trees provide a globular or globose drupe, with a thin or fibrous and relatively thick pericarp. The seed is ovoid or globose ascending, testa thin, thick or spongy, devoid of albumen, but with an embryo consisting mainly of two large cotyledons separate, free or more or less welded.
Des plantes du genre Calophyllum particulièrement concernées par la présente invention se trouvent dans la zone de l'Océan
Indien (par origine ou par introduction en culture). II s'agit notamment, mais non exclusivement des espèces suivantes Calophyllum eputamen Calophyllum inophyllum Calophyllum parviflorum Calophyllum soulattri Calophyllum tacamahaca Calophyllum spectabile Calophyllum recedens Calophyllum comorense Calophyllum Chapelieri Calophyllum Drouhardi Calophyllum laxiflorum.Plants of the genus Calophyllum particularly concerned by the present invention are found in the ocean zone
Indian (by origin or introduction to culture). These include, but are not limited to, the following species: Calophyllum eputamen Calophyllum inophyllum Calophyllum parviflorum Calophyllum calophyllum tacamahaca Calophyllum calophyllum Calophyllum calophyllum Calophyllum calophyllum Calophyllum calophyllum Calophyllum
De manière générale, les huiles extraites du fruit des plantes du genre Calophyllum sont visqueuses à température ambiante. In general, the oils extracted from the fruit of plants of the genus Calophyllum are viscous at room temperature.
Leur indice de réfraction est compris entre 1,4698 et 1,4715.Their refractive index is between 1.4698 and 1.4715.
Leur indice d'iode varie entre 68 et 91. Leur indice de saponification varie entre 180 et 215 mg KOH/g d'huile.Their iodine number varies between 68 and 91. Their saponification number varies between 180 and 215 mg KOH / g of oil.
Elles comprennent une fraction lipidique (98-99,5 % environ) et une fraction dite "insaponifiable" (0,5-2 % environ). They comprise a lipid fraction (about 98-99.5%) and a so-called "unsaponifiable" fraction (about 0.5-2%).
La fraction lipidique est principalement constituée de lipides neutres (90-92 % environ), de glycolipides (5-7 % environ), de phospholipides (1-2 % environ). The lipid fraction consists mainly of neutral lipids (about 90-92%), glycolipids (about 5-7%), phospholipids (about 1-2%).
L'étude de la composition des lipides neutres montre que les acides gras sont majoritaires dans ces lipides neutres
acide palmitique : 15-17 % environ acide palmitoleïque : 0,5-1 % environ acide stéarique : 8-16 % environ acide oléïque : 30-50 % environ acide linoléique : 25-40 % environ . acide arachidique : 0,5-1 % environ acide gadoléïque: 0,5-1 % environ
La fraction dite "insaponifiable" comprend différentes familles de composés, parmi lesquelles
des hydrocarbures à chaînes longues linéaires et/ou ramifiées, parfois insaturées des alcools gras des stérols, parmi lesquels du sitostérol et du stigmastérol, ainsi que des méthyl stérols des xanthones, notamment la caloxanthone des dérivés coumariniques et notamment les caloflorides, soulattrolides, calophyllolides ; des inophyllolides ou inophyllums ; les acides calophyllique, isocalophyllique, isopétalique, chapéliérique, pseudobrasilique des composés triterpéniques, notamment de la famille de la friedeline.The study of the composition of neutral lipids shows that fatty acids are the majority in these neutral lipids
palmitic acid: about 15-17% palmitoleic acid: about 0.5-1% stearic acid: about 8-16% oleic acid: about 30-50% linoleic acid: about 25-40%. arachidic acid: about 0.5-1% gadoleic acid: about 0.5-1%
The so-called "unsaponifiable" fraction comprises different families of compounds, among which
linear and / or branched long chain hydrocarbons, sometimes unsaturated fatty alcohols sterols, including sitosterol and stigmasterol, and methyl sterols xanthones, including caloxanthone coumarin derivatives including caloflorides, soulattrolides, calophyllolides; inophyllolides or inophyllums; the calophyllic, isocalophyllic, isopetalic, chapeleric, pseudobrasilic acids of triterpene compounds, especially of the friedeline family.
Les molécules qui confèrent les propriétés de filtre à bande large se trouvent dans cette fraction insaponifiable des huiles extraites des plantes du genre Callophyllum. The molecules that confer the broadband filter properties are found in this unsaponifiable fraction of oils extracted from plants of the genus Callophyllum.
Les techniques d'extraction des huiles sont développées à partir des techniques connues, par broyage ou par solvant. Oil extraction techniques are developed from known techniques, by grinding or by solvent.
On broie les fruits frais ou séchés, en totalité ou après décorticage de façon à obtenir les amandes qui représentent 4050 % environ du poids du fruit sec. The fresh or dried fruits are ground in whole or after dehulling to obtain the almonds which represent 4050% of the weight of the dry fruit.
On extrait l'huile par pression au moyen d'une presse mécanique. The oil is extracted by pressure by means of a mechanical press.
On obtient une huile verdâtre, avec un rendement de 40 à 75 % environ suivant les espèces de Callophyllum. A greenish oil is obtained, with a yield of about 40 to 75% depending on the Callophyllum species.
En variante, on utilise un solvant ou un mélange de solvant tels que l'éther de pétrole, le n-hexane, le cyclohexane, le pentane, le chlorure de méthylène, le chloroforme, le trichloroéthylène, le méthanol, I'éthanol, I'éther diéthylique,
I'éther diisopropylique, le dioxane, I'acétone, la méthyl éthyl cétone.Alternatively, a solvent or solvent mixture such as petroleum ether, n-hexane, cyclohexane, pentane, methylene chloride, chloroform, trichlorethylene, methanol, ethanol, is used. diethyl ether,
Diisopropyl ether, dioxane, acetone, methyl ethyl ketone.
On obtient l'huile par évaporation du solvant. The oil is obtained by evaporation of the solvent.
Ces huiles peuvent être ensuite décolorées et désodorisées par passage sur charbon actif ou terres décolorantes, leur odeur et leur goût étant peu agréables. These oils can then be discolored and deodorized by passage through activated charcoal or bleaching earths, their smell and taste being unpleasant.
On a constaté expérimentalement qu'une huile de ce type possède une absorption comparable à celle d'une molécule de synthèse. It has been found experimentally that an oil of this type has an absorption comparable to that of a synthetic molecule.
Ainsi, L'huile extraite des plantes du genre Calophyllum peut constituer une huile cosmétique, une huile destinée à la filtration des rayonnements ultraviolets, et être ainsi utilisée à des fins cosmétiques, ou pour la préparation d'une composition cosmétique, notamment destinée à filtrer les rayonnements solaires. Thus, the oil extracted from plants of the genus Calophyllum can constitute a cosmetic oil, an oil intended for the filtration of ultraviolet radiation, and thus be used for cosmetic purposes, or for the preparation of a cosmetic composition, in particular intended to filter solar radiation.
On a effectué une comparaison entre les propriétés filtrantes des rayonnements solaires d'une composition test à base d'huile extraite des plantes du genre Callophyllum selon l'invention et d'une composition cosmétique traditionnelle de référence à base d'octyl méthoxycinnamate, qui est un filtre solaire habituel des radiations UVB. A comparison was made between the solar radiation filtering properties of an oil-based test composition extracted from plants of the genus Callophyllum according to the invention and a traditional reference cosmetics composition based on octyl methoxycinnamate, which is a usual sun filter UVB radiation.
La composition test selon l'invention était constituée d'une solution d'huile de Callophyllum à 25 % dans de l'éthanol. The test composition according to the invention consisted of a solution of 25% Callophyllum oil in ethanol.
La composition de référence était constituée d'une solution d'octyl méthoxycinnamate (ester 2-éthylhexylique de l'acide 3-(4. The reference composition consisted of a solution of octyl methoxycinnamate (2-ethylhexyl ester of 3- (4.
méthoxyphényl)-prop-2-énoïque, CAS Registry Number 5466-773) à 3 % dans de l'éthanol.methoxyphenyl) -prop-2-enoic, CAS Registry Number 5466-773) at 3% in ethanol.
On a mesuré, pour sa longueur d'onde d'absorbance maximum et pour une longueur d'onde de référence, I'absorbance de chacune des compositions ci-dessus, exprimée suivant la formule
A = E.c.l où A est l'absorbance,
E est le coefficient d'extinction en l.g-1.cm-1 c est la concentration en 9.1-1. The absorbance of each of the above compositions, expressed according to the formula, was measured for its maximum absorbance wavelength and for a reference wavelength.
A = Ecl where A is the absorbance,
E is the extinction coefficient in lg-1.cm-1 c is the concentration in 9.1-1.
I est la longueur du trajet optique en cm. I is the length of the optical path in cm.
Les résultats sont réunis dans le Tableau ci-dessous
<tb> <SEP> )imax <SEP> Amax <SEP> | <SEP> A350
<tb> Composition <SEP> test
<tb> (Huile <SEP> de <SEP> Callophyllum) <SEP> 240 <SEP> 474
<tb> <SEP> 295 <SEP> 453
<tb> <SEP> 335 <SEP> 270 <SEP> 270
<tb> Composition <SEP> de <SEP> référence
<tb> (Octyl <SEP> cinnamate) <SEP> 311 <SEP> 699 <SEP> 48 <SEP>
<tb>
Ainsi, on a constaté que pour la longueur d'onde 350 nm (dernière colonne), la composition à base d'huile de Calophyllum selon l'invention était environ 5, 2 fois plus efficace que la composition de référence.<tb><SEP>) imax <SEP> Amax <SEP> | <SEP> A350
<tb> Composition <SEP> test
<tb> (Oil <SEP> of <SEP> Callophyllum) <SEP> 240 <SEP> 474
<tb><SEP> 295 <SEP> 453
<tb><SEP> 335 <SEP> 270 <SEP> 270
<tb> Composition <SEP> of <SEP> reference
<tb> (Octyl <SEP> cinnamate) <SEP> 311 <SEQ> 699 <SEP> 48 <SEP>
<Tb>
Thus, it was found that for the wavelength 350 nm (last column), the Calophyllum oil-based composition according to the invention was about 5.2 times more effective than the reference composition.
On trouvera ci-dessous deux exemples de compositions de protection solaire à base d'huile extraite des plantes du genre
Calophyllum selon l'invention.Two examples of oil-based sunscreen compositions extracted from plants of the genus are given below.
Calophyllum according to the invention.
EXEMPLE 1
Composition pour une huile solaire - huile de Calophyllum 25,0 9 - huile de tournesol 2,0 9 - beurre de karité 1,0 g
- acétate de vitamine E 0,3 g
- imidazolidinyl urée 0,2 g
- parfum qs
- alcool éthylique absolu qsp 100,0 g
EXEMPLE 2
Composition pour une émulsion solaire sous forme de gel-crème - huile de Calophyllum 15,0 g - polyglycéryl méthacrylate/propylène glycol15,0 g - méthyl paraben 0,3 g - glycérine 5,0 g - imidazolidinyl urée 0,2 g - conservateurs qs - parfum qs - eau qsp 100,0 g EXAMPLE 1
Composition for a solar oil - Calophyllum oil 25.0 9 - Sunflower oil 2.0 9 - Shea butter 1.0 g
- Vitamin E acetate 0.3 g
- imidazolidinyl urea 0.2 g
- perfume qs
- absolute ethyl alcohol qs 100.0 g
EXAMPLE 2
Composition for a solar emulsion in gel-cream form - Calophyllum oil 15.0 g - polyglyceryl methacrylate / propylene glycol 15.0 g - methyl paraben 0.3 g - glycerin 5.0 g - imidazolidinyl urea 0.2 g - preservatives qs - perfume qs - water qs 100.0 g
Claims (13)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9509123A FR2736827B1 (en) | 1995-07-21 | 1995-07-21 | COSMETIC OIL EXTRACTED FROM PLANTS OF THE CALOPHYLLUM TYPE |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9509123A FR2736827B1 (en) | 1995-07-21 | 1995-07-21 | COSMETIC OIL EXTRACTED FROM PLANTS OF THE CALOPHYLLUM TYPE |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| FR2736827A1 true FR2736827A1 (en) | 1997-01-24 |
| FR2736827B1 FR2736827B1 (en) | 1997-09-19 |
Family
ID=9481434
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR9509123A Expired - Fee Related FR2736827B1 (en) | 1995-07-21 | 1995-07-21 | COSMETIC OIL EXTRACTED FROM PLANTS OF THE CALOPHYLLUM TYPE |
Country Status (1)
| Country | Link |
|---|---|
| FR (1) | FR2736827B1 (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998037863A2 (en) * | 1997-02-25 | 1998-09-03 | Claude Boucher | Properties with synergistic effects between them and with natural extracts or natural substances, extracts and oils of plants of the genus calophyllum, bertholletia and moringa and their dietetic, cosmetic and therapeutic applications |
| FR2794973A1 (en) * | 1999-06-18 | 2000-12-22 | Mousny Brigitte | Calophyllum oil extracted at ambient temperature has UV protecting, antiradical, antioxidant, antiaging and therapeutic properties |
| FR2800275A1 (en) * | 1999-10-27 | 2001-05-04 | Jean Daniel Mondin | Composition for cosmetic or therapeutic use for treating skin contains hydro soluble excipient enabling the gelling of essential oils in the absence of all other oils |
| FR2858982A1 (en) * | 2003-08-18 | 2005-02-25 | Claude Boucher | Preparing plant oil by solvent-less pressing of powdered material, useful in e.g. cosmetic, food, pharmaceutical and agricultural compositions, gives product with improved oxidation resistance |
| FR3054241A1 (en) * | 2016-07-20 | 2018-01-26 | Phytobokaz | METHOD OF ISOLATING AND APPLYING RESIN OF "GALBA ® OIL" |
| FR3083451A1 (en) * | 2018-07-06 | 2020-01-10 | Qiriness | COSMETIC COMPOSITION COMPRISING A THREE-ACTIVE SOLAR COMPLEX |
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| EP0145607A2 (en) * | 1983-12-12 | 1985-06-19 | L'oreal | Aqueous or anhydrous cosmetic composition containing a fatty phase based on karite oil |
| EP0336902A2 (en) * | 1988-04-04 | 1989-10-11 | Warner-Lambert Company | Antiinflammatory skin moisturizing composition and method of preparing same |
| EP0336901A2 (en) * | 1988-04-04 | 1989-10-11 | Warner-Lambert Company | Anesthetic skin moisturizing composition and method of preparing same |
| JPH05294843A (en) * | 1992-04-17 | 1993-11-09 | Nippon Mektron Ltd | Agent active to eliminate active oxygen and agent having antiallergic action |
-
1995
- 1995-07-21 FR FR9509123A patent/FR2736827B1/en not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE673511A (en) * | 1964-12-17 | 1966-06-09 | ||
| EP0145607A2 (en) * | 1983-12-12 | 1985-06-19 | L'oreal | Aqueous or anhydrous cosmetic composition containing a fatty phase based on karite oil |
| EP0336902A2 (en) * | 1988-04-04 | 1989-10-11 | Warner-Lambert Company | Antiinflammatory skin moisturizing composition and method of preparing same |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998037863A2 (en) * | 1997-02-25 | 1998-09-03 | Claude Boucher | Properties with synergistic effects between them and with natural extracts or natural substances, extracts and oils of plants of the genus calophyllum, bertholletia and moringa and their dietetic, cosmetic and therapeutic applications |
| WO1998037863A3 (en) * | 1997-02-25 | 1999-02-18 | Claude Boucher | Properties with synergistic effects between them and with natural extracts or natural substances, extracts and oils of plants of the genus calophyllum, bertholletia and moringa and their dietetic, cosmetic and therapeutic applications |
| FR2794973A1 (en) * | 1999-06-18 | 2000-12-22 | Mousny Brigitte | Calophyllum oil extracted at ambient temperature has UV protecting, antiradical, antioxidant, antiaging and therapeutic properties |
| FR2800275A1 (en) * | 1999-10-27 | 2001-05-04 | Jean Daniel Mondin | Composition for cosmetic or therapeutic use for treating skin contains hydro soluble excipient enabling the gelling of essential oils in the absence of all other oils |
| FR2858982A1 (en) * | 2003-08-18 | 2005-02-25 | Claude Boucher | Preparing plant oil by solvent-less pressing of powdered material, useful in e.g. cosmetic, food, pharmaceutical and agricultural compositions, gives product with improved oxidation resistance |
| FR3054241A1 (en) * | 2016-07-20 | 2018-01-26 | Phytobokaz | METHOD OF ISOLATING AND APPLYING RESIN OF "GALBA ® OIL" |
| FR3083451A1 (en) * | 2018-07-06 | 2020-01-10 | Qiriness | COSMETIC COMPOSITION COMPRISING A THREE-ACTIVE SOLAR COMPLEX |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2736827B1 (en) | 1997-09-19 |
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