FR2867071A1 - Cosmetic or dermatological composition, useful for fighting against the effects of e.g. ageing, cellular hypophyxia and dehydration, comprises olive water concentrated in polyphenols and peroxidized olive oil - Google Patents
Cosmetic or dermatological composition, useful for fighting against the effects of e.g. ageing, cellular hypophyxia and dehydration, comprises olive water concentrated in polyphenols and peroxidized olive oil Download PDFInfo
- Publication number
- FR2867071A1 FR2867071A1 FR0402151A FR0402151A FR2867071A1 FR 2867071 A1 FR2867071 A1 FR 2867071A1 FR 0402151 A FR0402151 A FR 0402151A FR 0402151 A FR0402151 A FR 0402151A FR 2867071 A1 FR2867071 A1 FR 2867071A1
- Authority
- FR
- France
- Prior art keywords
- olive
- cosmetic
- polyphenols
- peroxidized
- dermatological composition
- 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.)
- Granted
Links
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Classifications
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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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/63—Oleaceae (Olive family), e.g. jasmine, lilac or ash tree
-
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/38—Percompounds, e.g. peracids
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
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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
-
- 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
- A61Q19/08—Anti-ageing preparations
Landscapes
- Health & Medical Sciences (AREA)
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- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Dermatology (AREA)
- Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Birds (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Emergency Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Gerontology & Geriatric Medicine (AREA)
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- Alternative & Traditional Medicine (AREA)
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- Medical Informatics (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Cosmetics (AREA)
Abstract
Description
COMPOSITION COSMETIQUE OU DERMATOLOGIQUE À BASE D'OLIVECOSMETIC OR DERMATOLOGICAL COMPOSITION BASED ON OLIVE
La présente invention a pour objet une composition cosmétique ou dermatologique à base d'huile d'olive et d'eau d'olive. The present invention relates to a cosmetic or dermatological composition based on olive oil and olive water.
L'olivier, Olea europea pour le botaniste, est originaire du bassin méditerranéen et sa culture existe depuis les premiers âges de l'humanité. En Europe, sa zone d'implantation est limitée au contour méditerranéen, mais il pousse aussi en Asie et en Afrique. Convenablement préparée, l'olive noire est un aliment riche en minéraux, vitamines, glucides et protides. Le fruit, l'olive et plus précisément son huile a de nombreuses propriétés médicinales. The olive tree, Olea europea for the botanist, is native to the Mediterranean basin and its culture has existed since the first ages of humanity. In Europe, its zone of implantation is limited to the Mediterranean outline, but it also grows in Asia and Africa. Properly prepared, the black olive is a food rich in minerals, vitamins, carbohydrates and proteins. The fruit, the olive and more precisely its oil has many medicinal properties.
Le fruit de l'olive contient des glucides (principalement des oses (mannitol), environ 10 à 20%), des protides (enzymes: diastases (émulsine, oléase), environ 5 à 10%), des lipides (triglycérides constitués d'acides gras (60 à 80 % d'acide oléique, 7 à 14 % d'acide palmitique, 5 à 15 % d'acide linoléique, 3 à 5 % d'acide stéarique, 1 à 3 % d'acide arachidique, 1 à 3% d'acide palmitoléique)), des matières minérales (calcium, fer, phosphore, potassium, silicium, sodium, environ 2%), des composés phénoliques (principalement des flavonoïdes), des terpénoïdes parmi lesquels des sécoiridoïdes (oleuropéoside) et des triterpènes (saponines (acide oléanolique)), des vitamines (vitamine A (rétinol), vitamine D (calciférol)), des insaponifiables formés de phénols (alphabeta-gamma-tocophérols), stéroïdes (campestérol, phytostérol, béta-sitostérol, stigmastérol) et squalène (environ 0,4 à 0,8 %). The fruit of the olive contains carbohydrates (mainly oses (mannitol), about 10 to 20%), proteins (enzymes: diastases (emulsin, oleasts), about 5 to 10%), lipids (triglycerides consisting of fatty acids (60 to 80% oleic acid, 7 to 14% palmitic acid, 5 to 15% linoleic acid, 3 to 5% stearic acid, 1 to 3% arachidic acid, 1 to 3% palmitoleic acid), mineral materials (calcium, iron, phosphorus, potassium, silicon, sodium, approximately 2%), phenolic compounds (mainly flavonoids), terpenoid compounds including secoiridoids (oleuropeoside) and triterpenes (saponins (oleanolic acid)), vitamins (vitamin A (retinol), vitamin D (calciferol)), unsaponifiables consisting of phenols (alphabeta-gamma-tocopherols), steroids (campesterol, phytosterol, beta-sitosterol, stigmasterol) and squalene (about 0.4 to 0.8%).
L'élément déterminant dans l'évaluation de la qualité nutritionnelle d'une huile est sa composition en 2867071 2 acides gras: saturés, monoinsaturés et polyinsaturés. Selon les nutritionnistes, l'apport idéal en graisse se composerait pour moitié d'acides gras monoinsaturés et pour un quart d'acides gras polyinsaturés. L'huile d'olive, selon l'année et le lieu de récolte peut renfermer jusqu'à 75 % d'acides gras monoinsaturés, c'est-à-dire d'acide oléique. Des huiles comme le maïs, le soja, le tournesol contiennent jusqu'à 60 % d'acides gras polyinsaturés, c'est-à-dire l'acide linoléïque et linolénique. De par sa composition équilibrée en acides gras, l'huile d'olive offre le meilleur équilibre nutritionnel au niveau cellulaire. The determining factor in the evaluation of the nutritional quality of an oil is its composition in 2867071 2 fatty acids: saturated, monounsaturated and polyunsaturated. According to nutritionists, the ideal fat intake would consist of half monounsaturated fatty acids and a quarter of polyunsaturated fatty acids. Depending on the year and the place of harvest, olive oil can contain up to 75% of monounsaturated fatty acids, that is to say oleic acid. Oils such as corn, soy, sunflower contain up to 60% polyunsaturated fatty acids, ie linoleic and linolenic acid. With its balanced composition of fatty acids, olive oil offers the best nutritional balance at the cellular level.
L'huile n'est pas le seul élément extrait du fruit de l'olivier. Le procédé d'extraction de l'olive est basé sur le principe suivant. broyage des olives, pressage à froid et centrifugation pour récupérer l'huile. Une tonne d'olives produit en moyenne 200 litres d'huile. Le reste, soit environ 800 kg par tonne est composé de sous-produits: les grignons d'olives (formés des pulpes et des noyaux après extraction de l'huile par pressage) et les effluents liquides ou eau du fruit, encore appelés margines. En volume, la fraction appelée margine (eau d'olive) est la plus importante tirée du fruit. Cette eau est fortement chargée en éléments minéraux et organiques. Oil is not the only element extracted from the fruit of the olive tree. The extraction process of the olive is based on the following principle. grinding olives, cold pressing and centrifugation to recover the oil. A ton of olives produces an average of 200 liters of oil. The remainder, about 800 kg per ton, is composed of by-products: olive cake (formed from pulp and stone after extraction of the oil by pressing) and liquid effluents or fruit water, also called vegetable water. In volume, the fraction called margine (olive water) is the most important from the fruit. This water is heavily loaded with mineral and organic elements.
L'élimination des margines non traitées pose un important problème de pollution de l'environnement, car ces eaux résiduaires sont quatre cent fois plus chargées que les eaux usées domestiques. Cette pollution pourrait être considérablement réduite si l'on parvenait à valoriser ces eaux. The elimination of untreated vegetable waters poses a significant environmental pollution problem, as these waste waters are four hundred times more charged than domestic wastewater. This pollution could be considerably reduced if these waters could be valorised.
Les margines sont des effluents très acides à forte charge saline et organique. Elles sont caractérisées par un pH d'environ 4,8 et une forte charge en minéraux: 2867071 3 ions potassium (5000 à 11000 mg/1), chlorure (600 à 1200 mg/1), calcium (200 à 700 mg/1), magnésium (130 à 290 mg/1) et phosphore (200 à 400 mg/1). Cette eau est également fortement chargée en éléments organiques comme les polyphénols. Les polyphénols se subdivisent en plusieurs sous-groupes dont les flavonoïdes. Du point de vue cosmétique, les flavonoïdes sont les anti-oxydants les plus efficaces, propriété qui repose sur le fait qu'ils sont à la fois solubles dans l'eau et dans les lipides. Vegetables are very acidic effluents with a high saline and organic load. They are characterized by a pH of approximately 4.8 and a high load of minerals: 2867071 3 potassium ions (5000 to 11000 mg / l), chloride (600 to 1200 mg / l), calcium (200 to 700 mg / l) ), magnesium (130 to 290 mg / l) and phosphorus (200 to 400 mg / l). This water is also heavily loaded with organic elements such as polyphenols. Polyphenols are subdivided into several subgroups including flavonoids. From the point of view of cosmetics, flavonoids are the most effective antioxidants, which is based on the fact that they are both soluble in water and in lipids.
Les travaux réalisés par la Demanderesse concernent plus particulièrement le bénéfice cosmétique ou dermatologique obtenu sur la peau, par la combinaison originale de deux éléments extraits de l'olive: l'eau d'olive et l'huile d'olive. The work carried out by the Applicant relates more particularly to the cosmetic or dermatological benefit obtained on the skin, by the original combination of two elements extracted from the olive: olive water and olive oil.
L'invention a donc pour objet une composition cosmétique ou dermatologique, caractérisée en ce qu'elle comprend une eau d'olive concentrée en polyphénols et une huile d'olive peroxydée. The subject of the invention is therefore a cosmetic or dermatological composition, characterized in that it comprises an olive water concentrated in polyphenols and a peroxidized olive oil.
Par eau d'olive, on entend une eau ou un extrait d'eau provenant du fruit de l'olive. Olive water is water or water extract from the fruit of the olive.
Par eau d'olive concentrée en polyphénols, on entend une eau du fruit de l'olive (naturellement riche en polyphénols) qui a été concentrée par évaporation jusqu'à obtenir un actif anti-radicalaire plus efficace que les anti-radicalaires connus. De manière avantageuse, l'eau d'olive concentrée en polyphénols présente donc une activité anti-radicalaire particulièrement élevée. Olive water concentrated in polyphenols means water from the olive fruit (naturally rich in polyphenols) which has been concentrated by evaporation to obtain a more effective anti-radical active agent than known anti-radicals. Advantageously, the olive water concentrated in polyphenols thus has a particularly high anti-radical activity.
L'huile d'olive peroxydée est un agent apaisant et désensibilisant obtenu par un procédé d'oxydation contrôlé et fabriqué spécialement pour la cosmétique de la Demanderesse. La transformation de l'huile d'olive en huile d'olive peroxydée confère à l'huile d'olive de nouvelles propriétés avantageuses, 2867071 4 permettant notamment de résoudre le problème de l'hypophyxie cellulaire de la peau. En effet, au niveau cellulaire, l'équilibre nutritionnel est sous la dépendance d'un élément indispensable à la cellule. Peroxidized olive oil is a soothing and desensitizing agent obtained by a controlled oxidation process and manufactured especially for the cosmetics of the Applicant. The transformation of olive oil into peroxidized olive oil confers on olive oil new advantageous properties, 2867071 4 in particular making it possible to solve the problem of cellular hypophyxia of the skin. Indeed, at the cellular level, the nutritional equilibrium is dependent on an element essential to the cell.
l'oxygène. L'oxygène est véhiculé par le sang; en vieillissant, les cellules ne sont plus suffisamment oxygénées, leur métabolisme se ralentit, la peau devient terne puis se fragilise et se ride. À 20 ans, la teneur en oxygène dans la peau atteint un niveau maximal; à 30 ans: le taux d'oxygène diminue de 25 % et à 40 ans: le taux d'oxygène diminue de 50 %. Ainsi, de manière avantageuse, une composition cosmétique ou dermatologique comprenant de l'huile d'olive peroxydée permet de mieux nourrir les tissus de la peau car ils sont mieux oxygénés, d'augmenter le flux sanguin cinq minutes après application de la composition et de relancer le métabolisme des cellules cutanées. oxygen. Oxygen is carried by the blood; as they age, the cells are no longer sufficiently oxygenated, their metabolism slows down, the skin becomes dull and then becomes fragile and wrinkled. At age 20, the oxygen content in the skin reaches a maximum level; at 30 years: the oxygen level decreases by 25% and at 40 years: the oxygen level decreases by 50%. Thus, advantageously, a cosmetic or dermatological composition comprising peroxidized olive oil makes it possible to better nourish the tissues of the skin because they are better oxygenated, to increase the blood flow five minutes after application of the composition and to revive the metabolism of cutaneous cells.
Les travaux de la Demanderesse ont permis de mettre en évidence que l'association de l'eau du fruit de l'olive, qui présente une activité anti-radicalaire élevée, avec de l'huile d'olive peroxydée, qui dynamise le métabolisme cellulaire, permet d'obtenir des compositions cosmétiques ou dermatologiques protégeant remarquablement bien la peau des agressions quotidiennes qu'elle subit, telles que le stress, la fatigue, la pollution ou le tabac. The work of the Applicant has made it possible to demonstrate that the combination of olive fruit water, which has a high anti-radical activity, with peroxidized olive oil, which boosts cellular metabolism. , makes it possible to obtain cosmetic or dermatological compositions that remarkably protect the skin from the daily aggressions that it undergoes, such as stress, fatigue, pollution or tobacco.
L'eau d'olive concentrée en polyphénols est présente dans la composition de l'invention en une quantité allant de 0,1 % à 50 %, de préférence de 0, 5 % à 30 % et tout préférentiellement de 0,5 % à 20 % en poids par rapport au poids total de la composition. The olive water concentrated in polyphenols is present in the composition of the invention in an amount ranging from 0.1% to 50%, preferably from 0.5% to 30% and most preferably from 0.5% to 20% by weight relative to the total weight of the composition.
L'eau d'olive concentrée en polyphénols comprend 5% de polyphénols. Olive water concentrated in polyphenols contains 5% polyphenols.
2867071 5 L'eau d'olive concentrée en polyphénols peut être obtenue par exemple par évaporation ménagée. The olive water concentrated in polyphenols can be obtained for example by gentle evaporation.
L'huile d'olive peroxydée est présente dans la composition de l'invention en une quantité allant de 0,1 % à 40 %, de préférence de 0,5 % à 30 % et tout préférentiellement de 0,5 % à 20 % en poids par rapport au poids total de la composition. Peroxidized olive oil is present in the composition of the invention in an amount ranging from 0.1% to 40%, preferably from 0.5% to 30% and most preferably from 0.5% to 20% by weight relative to the total weight of the composition.
L'huile d'olive peroxydée présente un indice de peroxyde compris entre 50 et 90 mEg/kg. Peroxidized olive oil has a peroxide value of 50 to 90 mEg / kg.
L'huile d'olive peroxydée peut être obtenue par exemple par barbotage d'un flux d'oxygène pur. Peroxidized olive oil can be obtained for example by bubbling a stream of pure oxygen.
Les compositions selon l'invention peuvent également comprendre d'autres actifs généralement utilisés en cosmétique ou dermatologie, comme par exemple des agents hydratants, restructurants, séborrégulateurs, antiinflammatoires et antiseptiques de la peau. Ces actifs, s'ils sont présents, peuvent représenter de 0,1 % à 50 %, de préférence de 0,5 % à 15 % en poids de la composition. The compositions according to the invention may also comprise other active agents generally used in cosmetics or dermatology, for example moisturizing, restructuring, seborrégulateurs, anti-inflammatory and antiseptic agents of the skin. These active agents, if present, can represent from 0.1% to 50%, preferably from 0.5% to 15% by weight of the composition.
Les compositions de l'invention sont tout particulièrement destinées aux soins de la peau du visage et du corps. The compositions of the invention are particularly intended for the care of the skin of the face and body.
Les compositions selon l'invention peuvent se présenter sous toutes les formes galéniques classiquement utilisées, et bien connues de l'homme de l'art, dans les domaines cosmétiques ou dermatologiques pour être appliquées sur la peau, comme par exemple, des émulsions Huile dans Eau (H/E) ou Eau dans Huile (E/H), des lotions, shampooings, sprays, gels ou gels moussants pour la douche, des laits, des masques, des crèmes, etc. sans aucune restriction galénique particulière autre que celles 2867071 6 de la compatibilité avec l'eau d'olive et l'huile d'olive à la base de la composition. The compositions according to the invention may be in any of the galenical forms conventionally used, and well known to those skilled in the art, in the cosmetic or dermatological fields to be applied to the skin, for example, oil emulsions. Water (O / W) or Water in Oil (W / O), lotions, shampoos, sprays, gels or bubble gels for showering, milks, masks, creams, etc. without any particular pharmaceutical restrictions other than those of the compatibility with the olive water and the olive oil at the base of the composition.
Ainsi, les compositions de l'invention peuvent aussi contenir tous les constituants classiquement utilisés dans ces présentations comme des agents de formulation, des agents tensio-actifs, des agents conservateurs, des agents solubilisants, des agents gélifiants, des additifs gras non végétaux, du propylène glycol, du sorbitol, du glycérol, de la triéthanolamine, des bases de parfums, de l'eau en quantité suffisante pour 100. Thus, the compositions of the invention may also contain all the constituents conventionally used in these presentations as formulating agents, surfactants, preserving agents, solubilizing agents, gelling agents, non-vegetable fatty additives, propylene glycol, sorbitol, glycerol, triethanolamine, perfume bases, water in sufficient quantity for 100.
Ainsi, l'invention a aussi pour objet une méthode de soin cosmétique consistant à appliquer sur la peau une quantité adéquate d'une composition telle que définie précédemment. Thus, the invention also relates to a cosmetic care method consisting in applying to the skin an adequate amount of a composition as defined above.
L'invention a également pour objet l'utilisation d'une eau d'olive concentrée en polyphénols en combinaison avec une huile d'olive peroxydée, pour la préparation d'une composition cosmétique ou dermatologique. The invention also relates to the use of an olive water concentrated polyphenols in combination with a peroxidized olive oil for the preparation of a cosmetic or dermatological composition.
Les compositions cosmétiques ou dermatologiques ainsi préparées permettent de lutter contre les effets du vieillissement tels que les rides, l'hypophyxie cellulaire, la déshydratation, la perte de souplesse et de résistance de la peau et des micro-vaisseaux sanguins. The cosmetic or dermatological compositions thus prepared make it possible to combat the effects of aging, such as wrinkles, cellular hypophyxia, dehydration, the loss of flexibility and resistance of the skin and of the micro-blood vessels.
Elles permettent également de lutter contre les agressions quotidiennes subies par la peau telles que le stress, la fatigue, la pollution ou le tabac. They also make it possible to fight against daily aggressions suffered by the skin such as stress, fatigue, pollution or tobacco.
Les compositions de l'invention peuvent donc être avantageusement utilisées à diverses fins: anti-âge (notamment anti-rides), anti-stress ou anti-pollution. The compositions of the invention can therefore be advantageously used for various purposes: anti-aging (especially anti-wrinkle), anti-stress or anti-pollution.
2867071 72867071 7
Description des figuresDescription of figures
La figure 1 représente le pourcentage d'inhibition du radical DPPH en fonction de la concentration de différentes crèmes. FIG. 1 represents the percentage of inhibition of the DPPH radical as a function of the concentration of different creams.
La courbe reliée par le symbole du carré représente le pourcentage d'inhibition du DPPH en fonction de la concentration de la crème Visage Quotidienne Olive de l'invention. The curve connected by the square symbol represents the percent inhibition of DPPH as a function of the concentration of the Daily Olive Face Cream of the invention.
La courbe reliée par le symbole du losange représente le pourcentage d'inhibition du DPPH en fonction de la concentration de la crème Visage SPF15 de l'invention. The curve connected by the diamond symbol represents the percentage inhibition of DPPH as a function of the concentration of the cream SPF15 face of the invention.
La courbe reliée par le symbole du triangle représente le pourcentage d'inhibition du DPPH en fonction de la concentration d'une crème de composition identique à celle de la crème Visage Quotidienne Olive de l'invention mais ne contenant pas les actifs de cette crème. The curve connected by the symbol of the triangle represents the percentage inhibition of the DPPH as a function of the concentration of a cream of composition identical to that of the Daily Olive face cream of the invention but not containing the active ingredients of this cream.
La courbe reliée par le symbole de la croix représente le pourcentage d'inhibition du DPPH en fonction de la concentration d'une crème de composition identique à celle de la crème Visage SPF15 de l'invention mais ne contenant pas les actifs de cette crème. The curve connected by the symbol of the cross represents the percentage inhibition of the DPPH as a function of the concentration of a cream of composition identical to that of the SPF15 face cream of the invention but not containing the active ingredients of this cream.
La figure 2 représente le pourcentage d'inhibition du radical DPPH en fonction de la concentration de différentes crèmes. FIG. 2 represents the percentage of inhibition of the DPPH radical as a function of the concentration of different creams.
La courbe reliée par le symbole du carré gris représente le pourcentage d'inhibition du DPPH en fonction de la concentration de la crème Visage quotidienne Olive de l'invention. The curve connected by the gray square symbol represents the percent inhibition of DPPH as a function of the concentration of the Olive Daily Face cream of the invention.
La courbe reliée par le symbole du rond représente le pourcentage d'inhibition du DPPH en fonction 2867071 8 de la concentration de la crème Visage SPF15 de l'invention. The curve connected by the circle symbol represents the percent inhibition of DPPH as a function of the concentration of the SPF15 Face Cream of the invention.
La courbe reliée par le symbole du carré noir représente le pourcentage d'inhibition du DPPH en fonction de la concentration de la crème Vinopulp de l'art antérieur. The curve connected by the symbol of the black square represents the percentage inhibition of the DPPH as a function of the concentration of the Vinopulp cream of the prior art.
D'autres caractéristiques et avantages de la présente invention apparaîtront à la lecture des exemples non limitatifs qui suivent. Other characteristics and advantages of the present invention will appear on reading the following nonlimiting examples.
Exemple 1: Test OXYPRES permettant de mettre en évidence l'activité antiradicalaire de l'eau du fruit de l'olive. Example 1: OXYPRES test to highlight the antiradical activity of the water of the olive fruit.
Le test OXYPRES est un test permettant de mesurer l'oxydation d'un composé. The OXYPRES test is a test to measure the oxidation of a compound.
Les radicaux libres sont des agents oxydants très agressifs contre certains constituants de l'organisme en général, et de la peau en particulier (enzymes, acides nucléiques, collagène, élastine, acide hyaluronique), ce qui aboutit à la sclérose et à la fibrose, indices les plus visibles du vieillissement cutané. Le teint est terne et fatigué. Il est largement admis que la pollution et le stress sont parmi les principaux responsables des effets nocifs induits par les radicaux libres. Free radicals are very aggressive oxidizing agents against certain constituents of the body in general, and of the skin in particular (enzymes, nucleic acids, collagen, elastin, hyaluronic acid), which leads to sclerosis and fibrosis, most visible signs of skin aging. The complexion is dull and tired. It is widely accepted that pollution and stress are among the major contributors to the harmful effects of free radicals.
L'activité anti-radicalaire ou anti-oxydante de l'eau du fruit de l'olive a été comparée avec celle d'anti-radicalaires connus: Coenzyme Q10, les oligomères procyanolidiques (OPC) de raisin et la vitamine E. Ces activités ont été mises en évidence et quantifiées par le test OXYPRES. The anti-free radical or antioxidant activity of olive fruit water was compared with that of known anti-radicals: Coenzyme Q10, procyanolidic oligomers (OPC) grapes and vitamin E. These activities have been highlighted and quantified by the OXYPRES test.
Une émulsion cosmétique (émulsion H/E) est placée dans un récipient hermétique thermostaté à 90 C 2867071 9 dans une atmosphère d'oxygène pur à la pression initiale de 5 bars. La pression d'oxygène dans le récipient, mesurée en continu, chute brutalement quand l'émulsion commence à s'oxyder. A cosmetic emulsion (O / W emulsion) is placed in a sealed thermostatic container at 90 ° C in a pure oxygen atmosphere at the initial pressure of 5 bar. The oxygen pressure in the container, measured continuously, falls sharply when the emulsion begins to oxidize.
On appelle période d'induction, la durée écoulée entre le début de la mesure et la chute brutale de la pression d'oxygène. The induction period is the time elapsed between the start of the measurement and the sudden drop in oxygen pressure.
On définit le facteur de protection (FP) comme le rapport de la période d'induction de l'échantillon avec l'anti-oxydant sur la période d'induction du témoin (émulsion sans anti-oxydant). The protection factor (FP) is defined as the ratio of the induction period of the sample with the antioxidant over the induction period of the control (emulsion without antioxidant).
Les mesures du facteur de protection sont obtenues en utilisant dans l'émulsion une concentration de 0,1% d'anti-oxydant. L'activité de l'anti-oxydant, mise en évidence à l'aide d'un substrat peroxydable, est extrapolée à une activité anti- radicalaire potentielle. The protective factor measurements are obtained by using in the emulsion a concentration of 0.1% of antioxidant. The activity of the antioxidant, evidenced using a peroxidic substrate, is extrapolated to a potential anti-radical activity.
Sur une échelle de 5, le facteur de protection est égal à : - 1,2 pour le coenzyme Q10, - 1,4 pour les OPC de raisin, - 2,8 pour la vitamine E et, 4 pour l'eau d'olive concentrée en polyphénols. On a scale of 5, the protection factor is: - 1,2 for coenzyme Q10, - 1,4 for grape OPC, - 2,8 for vitamin E and, 4 for water of olive concentrated in polyphenols.
L'eau du fruit de l'olive présente donc une activité anti-radicalaire plus efficace que les antiradicalaires connus. Olive fruit water therefore has a more effective anti-radical activity than known antiradicals.
Exemple 2: Comparaison de la composition de différentes crèmes de l'invention avec une crème de l'art antérieur. Example 2 Comparison of the Composition of Different Creams of the Invention with Cream of the Prior Art
2867071 10 Composition 1: Crème Visage Quotidienne Olive de l'invention. Composition 1: Daily Olive Face Cream of the invention.
Emulsionnants 5 % Co-émulsionnants 1 % Alcool cétylique 1,5 % Huile d'olive A.O.0 2 % Huile d'olive peroxydée 1 % Beurre de karité 1 % Oléate de décyle 1,5 % Cire d'abeille 0,5 % Xanthane 0,8 % Glycérine 5 % Polyacrylamide 1,1 % Eau d'olive (margine) concentrée en polyphénols 1,4 % Eau qs Parfum qs Conservateur qs Les pourcentages indiqués ci-dessus et ci-après représentent le pourcentage en poids par rapport au poids total de la composition. Emulsifiers 5% Co-emulsifiers 1% Cetyl Alcohol 1.5% Olive Oil AO0 2% Peroxidized Olive Oil 1% Shea Butter 1% Decyl Oleate 1.5% Beeswax 0.5% Xanthan 0.8% Glycerine 5% Polyacrylamide 1.1% Olive water (vegetable water) concentrated in polyphenols 1.4% Water qs Fragrance qs Preservative qs The percentages given above and below represent the percentage by weight relative to total weight of the composition.
Composition 2 Crème Visage SPF15 de l'invention. Composition 2 Face Cream SPF15 of the invention.
Emulsionnants 5 % Co-émulsionnants 1 % Huile d'olive A.O.0 1 % Huile d'olive peroxydée 1 % Filtres solaires 12,5 % C12-15 alkylbenzoate 1 % Glycérine 5 % Gélifiant 0,4 % 10 15 20 2867071 11 Diméthicone 1,5 % Eau d'olive (margine) concentrée en polyphénols 1,4 % Eau qs Parfum qs Conservateur qs SPF signifie en anglais Sun Protection Factor . Autrement dit la crème Visage SPF15 a été formulée pour offrir une protection anti- solaire forte. Emulsifiers 5% Co-emulsifiers 1% Olive oil AO0 1% Peroxidized olive oil 1% Solar filters 12.5% C12-15 alkylbenzoate 1% Glycerin 5% Gelling agent 0.4% 10 15 20 2867071 11 Dimethicone 1 , 5% Olive water (vegetable water) concentrated in polyphenols 1.4% Water qs Perfume qs Preservative qs SPF stands for Sun Protection Factor. In other words, the SPF15 Face Cream has been formulated to provide strong sun protection.
Les tests d'usage de la crème Visage SPF15 menés sur 23 volontaires (12 femmes et 11 hommes) ayant un teint terne et fatigué donnent les résultats ci-joints: - texture onctueuse: 96%, - peau plus douce: 91%, protection de la peau contre les effets néfastes de la pollution: 84%, la peau retrouve son éclat et son équilibre naturel: 65%. The tests of use of the SPF15 face cream conducted on 23 volunteers (12 women and 11 men) having a dull and tired complexion give the attached results: - smooth texture: 96%, - softer skin: 91%, protection of the skin against the harmful effects of pollution: 84%, the skin regains its radiance and its natural balance: 65%.
Composition 3: Crème anti-radicalaire de l'art antérieur Vinopulp Les constituants sont: Propylène glycol Dicaprylate-dicaprate Butylène glycol Diméthicone Alcool cétylique Glycéryl stéarate Polyacrylamide Squalane Tocophéryl acétate Olygomères procyanidoliques de raisins 30 Tétrasodium EDTA Potassium sorbate Eau Parfum Conservateur Exemple 3: Mise en évidence des effets bénéfiques cosmétiques ou dermatologiques induits par l'association originale des deux actifs: huile d'olive peroxydée et eau d'olive concentrée en polyphénols. Composition 3: Anti-free radical cream of the prior art Vinopulp The constituents are: Propylene glycol Dicaprylate-dicaprate Butylene glycol Dimethicone Cetyl alcohol Glyceryl stearate Polyacrylamide Squalane Tocopheryl acetate Procyanidolic prochyroid-oligomers Tetrasodium EDTA Potassium sorbate Water Fragrance Preservative Example 3: Implementation evidence of the beneficial cosmetic or dermatological effects induced by the original combination of the two active ingredients: peroxidized olive oil and olive water concentrated in polyphenols.
Après de nombreux essais, la Demanderesse a sélectionné le test au DPPH pour sa fiabilité et sa reproductibilité. Ce test a permis de mettre en évidence un effet protecteur des crèmes de l'invention, vis-à-vis des radicaux libres, très efficace et inégalé à ce jour. After many trials, the Applicant has selected the DPPH test for its reliability and reproducibility. This test has made it possible to demonstrate a protective effect of the creams of the invention, with respect to free radicals, which is very effective and unequaled to date.
TEST AU DPPH: le DPPH (2,2'-diphényl-lpicrilhydrazyl) est un radical stabilisé par résonance qui possède la particularité d'être de couleur violette en solution. Lorsqu'il réagit avec un composé antiradicalaire, il se transforme en un autre produit qui, lui, n'est plus violet. Cette propriété permet de suivre l'évolution de la concentration du DPPH en présence de compositions anti-radicalaires. En effet, à l'aide d'un spectromètre visible calibré sur la longueur d'onde 1=515 nm (qui correspond au maximum d'absorption dans le violet), on peut facilement déterminer la concentration en DPPH. Plus le signal obtenu à cette longueur d'onde est faible, meilleur est l'efficacité anti-radicalaire de la composition. DPPH TEST: DPPH (2,2'-diphenyl-1-pyrilhydrazyl) is a resonance stabilized radical which has the particularity of being violet in solution. When it reacts with an antiradical compound, it turns into another product that is no longer purple. This property makes it possible to follow the evolution of the concentration of DPPH in the presence of anti-radical compositions. Indeed, using a visible spectrometer calibrated on the wavelength 1 = 515 nm (which corresponds to the maximum absorption in the violet), one can easily determine the concentration of DPPH. The lower the signal obtained at this wavelength, the better the anti-radical efficiency of the composition.
Pour classer les anti-radicalaires par ordre d'efficacité, on détermine l'EC50, qui est la concentration en composé actif (ou anti-radicalaire) 2867071 13 nécessaire pour bloquer 50% des radicaux. Une fois l'EC50 déterminé, on peut classer les compositions en fonction de leur efficacité anti-radicalaire. To classify the anti-radicals in order of effectiveness, the EC50 is determined, which is the concentration of active compound (or anti-radical) required to block 50% of the radicals. Once the EC50 is determined, the compositions can be classified according to their anti-radical efficiency.
Mode opératoire: É Solution DPPH: 50 mg/1 dans du méthanol. Procedure: DPPH solution: 50 mg / l in methanol.
É Solution de la crème à tester: 30 mg de la crème dans 5 ml de méthanol, puis une gamme de différentes concentrations en fonction de ce premier résultat. É Solution of the cream to be tested: 30 mg of the cream in 5 ml of methanol, then a range of different concentrations according to this first result.
Chaque expérience est effectuée trois fois. Each experiment is performed three times.
Dans une cuve en plastique de 1,5 ml, 1 ml de solution de DPPH dans le méthanol (50 mg/1) est mélangé avec 25 ml d'une solution de la crème telle que préparée précédemment. La cuvette est recouverte d'un parafilm pour éviter toute évaporation de solvant. Le mélange réagit pendant une heure et demie et la lecture par spectrométrie visible est effectuée à 515 nm. In a 1.5 ml plastic tub, 1 ml of DPPH solution in methanol (50 mg / l) is mixed with 25 ml of a solution of the cream as prepared above. The bowl is covered with a parafilm to prevent evaporation of solvent. The mixture reacts for one and a half hours and the visible spectrometry reading is carried out at 515 nm.
(1) Comparaison de l'activité anti-radicalaire de crèmes de l'invention avec des crèmes ne contenant pas les actifs des crèmes de l'invention. (1) Comparison of the anti-radical activity of creams of the invention with creams not containing the active ingredients of the creams of the invention.
Les compositions de l'invention décrites dans l'exemple 2, à savoir la crème Visage Quotidienne Olive et la crème Visage SPF15 ont été reformulées sans les actifs, à savoir sans eau d'olive concentrée en polyphénols et sans huile d'olive peroxydée. The compositions of the invention described in Example 2, namely the Olive Daily Face Cream and the SPF15 Face Cream were reformulated without the active ingredients, namely without olive water concentrated in polyphenols and without peroxidized olive oil.
La comparaison des crèmes avec et sans actifs est illustrée sur la figure n l. The comparison of creams with and without active ingredients is illustrated in FIG.
Le test au DPPH montre que les nouvelles formules de l'invention sont beaucoup plus efficaces dans la lutte contre les radicaux libres que des formules comparables mais ne contenant ni eau d'olive concentrée en polyphénols, ni huile d'olive peroxydée. La figure 1 met en évidence le remarquable effet anti-radicalaire obtenu 2867071 14 avec les compositions de l'invention comprenant une eau d'olive concentrée en polyphénols et une huile d'olive peroxydée. The DPPH test shows that the new formulas of the invention are much more effective in the fight against free radicals than comparable formulas but containing neither olive water concentrated in polyphenols nor peroxidized olive oil. Figure 1 shows the remarkable anti-radical effect obtained with the compositions of the invention comprising an olive water concentrated polyphenols and a peroxidized olive oil.
(2) Comparaison des crèmes de l'invention avec une crème de l'art antérieur Vinopulp . (2) Comparison of the creams of the invention with a cream of the prior art Vinopulp.
L'efficacité anti-radicalaire des deux crèmes visage olive Visage Quotidienne Olive et Visage SPF15 a été comparée à celle de la crème Vinopulp de l'art antérieur (dont la composition a été décrite dans l'exemple 2) de Caudalie. Caudalie se réclame être le seul laboratoire à utiliser les OPC de raisin qui permettent de protéger de façon inégalée la peau contre les radicaux libres . The anti-radical efficacy of the two face creams olive Face Daily Olive and Face SPF15 was compared with that of the cream Vinopulp of the prior art (whose composition was described in Example 2) of Caudalie. Caudalie claims to be the only laboratory to use grape OPCs that provide unparalleled skin protection against free radicals.
Les résultats obtenus sont représentés sur la figure 2. The results obtained are shown in FIG.
Le test au DPPH est très explicite: à la concentration en crème de 8000 ppm qui est la plus près de l'utilisation normale, on constate que pour la crème Visage Quotidienne Olive on obtient un pourcentage d'inhibition du DPPH (encore appelé coefficient d'extinction) de 38 % + 2%, alors que avec la crème de l'art antérieur on n'obtient que 17 % + 1% dans les mêmes conditions. L'activité anti-radicalaire est maximale pour la crème Visage Quotidienne Olive tandis que celle conférée par les OPC de raisin est faible puisqu'elle présente un coefficient d'extinction de 17%. The DPPH test is very explicit: at the cream concentration of 8000 ppm, which is closest to normal use, it is found that for the Olive Daily Face cream a percentage of DPPH inhibition (also known as extinction) of 38% + 2%, whereas with the cream of the prior art only 17% + 1% is obtained under the same conditions. The anti-free radical activity is maximum for the Olive Daily Face Cream while that conferred by the Grape OPC is low since it has an extinction coefficient of 17%.
La crème Visage SPF 15 présente une protection anti-radicalaire moins élevée que la crème Visage quotidienne olive sans SPF . Cependant, la crème avec SPF reste plus efficace contre les rayons solaires. The SPF 15 Face Cream has a lower anti-free radical protection than the Olive Daily Face Cream without SPF. However, the cream with SPF remains more effective against the sun's rays.
2867071 15 Le test au DDPH a permis de démontrer la très nette supériorité des crèmes de l'invention, qui sont de meilleurs facteurs de lutte contre les attaques anti- radicalaires (pollution, fumée, rayons solaires, tabac, 5 alcool, stress). The DDPH test has made it possible to demonstrate the very clear superiority of the creams of the invention, which are better factors for combating anti-radical attacks (pollution, smoke, sunlight, tobacco, alcohol, stress).
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FR0402151A Expired - Fee Related FR2867071B1 (en) | 2004-03-02 | 2004-03-02 | COSMETIC OR DERMATOLOGICAL COMPOSITION BASED ON OLIVE |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006084658A1 (en) * | 2005-02-10 | 2006-08-17 | Indena S.P.A. | Oral compositions for the prevention of uv damages |
WO2011018579A1 (en) | 2009-08-11 | 2011-02-17 | Totum Bio Cosmetics | Method for preparing whole olive juice, composition produced according to the method, and use thereof in the field of cosmetics and dietetics |
Citations (10)
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FR1354857A (en) * | 1962-12-11 | 1964-03-13 | Skin care products and process for their preparation | |
FR2461744A1 (en) * | 1979-07-19 | 1981-02-06 | Desjonqueres Stephane | Peroxidation of fats, esp. vegetable oils, using air - at higher temp. to give therapeutically more active product, used in foods and cosmetics |
FR2750331A1 (en) * | 1996-06-28 | 1998-01-02 | Rivadis Lab | Cosmetic composition for preventing scabs, micro-circulatory disorders and dry skin conditions |
FR2753374A1 (en) * | 1996-09-19 | 1998-03-20 | Rivadis Lab | Skin care composition contains peroxidised fatty substance e.g. unsaturated vegetable oils and plant extract |
JP2000319161A (en) * | 1999-03-09 | 2000-11-21 | Kanebo Ltd | Skin cosmetic |
WO2001045514A1 (en) * | 1999-12-20 | 2001-06-28 | Usana, Inc. | Antioxidant compositions extracted from olives and olive by-products |
EP1230926A1 (en) * | 1999-10-14 | 2002-08-14 | The Nisshin Oil Mills, Ltd. | Skin-care agents, skin antiaging agents, whitening agents and external skin preparations |
FR2825022A1 (en) * | 2001-05-23 | 2002-11-29 | Seppic Sa | Nontherapeutic treatment of the human or animal body comprises administering or applying olive polyphenols |
EP1310175A2 (en) * | 2001-11-08 | 2003-05-14 | Cognis Deutschland GmbH & Co. KG | Process for the isolation of antioxidants |
EP1378491A1 (en) * | 2002-07-01 | 2004-01-07 | Centre De Cooperation International En Recherche Agronomique Pour Le Developpement | Process of treating an aqueous extract of vegetable origin with biopolymer additive and powder produced by spraying it |
-
2004
- 2004-03-02 FR FR0402151A patent/FR2867071B1/en not_active Expired - Fee Related
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1354857A (en) * | 1962-12-11 | 1964-03-13 | Skin care products and process for their preparation | |
FR2461744A1 (en) * | 1979-07-19 | 1981-02-06 | Desjonqueres Stephane | Peroxidation of fats, esp. vegetable oils, using air - at higher temp. to give therapeutically more active product, used in foods and cosmetics |
FR2750331A1 (en) * | 1996-06-28 | 1998-01-02 | Rivadis Lab | Cosmetic composition for preventing scabs, micro-circulatory disorders and dry skin conditions |
FR2753374A1 (en) * | 1996-09-19 | 1998-03-20 | Rivadis Lab | Skin care composition contains peroxidised fatty substance e.g. unsaturated vegetable oils and plant extract |
JP2000319161A (en) * | 1999-03-09 | 2000-11-21 | Kanebo Ltd | Skin cosmetic |
EP1230926A1 (en) * | 1999-10-14 | 2002-08-14 | The Nisshin Oil Mills, Ltd. | Skin-care agents, skin antiaging agents, whitening agents and external skin preparations |
WO2001045514A1 (en) * | 1999-12-20 | 2001-06-28 | Usana, Inc. | Antioxidant compositions extracted from olives and olive by-products |
FR2825022A1 (en) * | 2001-05-23 | 2002-11-29 | Seppic Sa | Nontherapeutic treatment of the human or animal body comprises administering or applying olive polyphenols |
EP1310175A2 (en) * | 2001-11-08 | 2003-05-14 | Cognis Deutschland GmbH & Co. KG | Process for the isolation of antioxidants |
EP1378491A1 (en) * | 2002-07-01 | 2004-01-07 | Centre De Cooperation International En Recherche Agronomique Pour Le Developpement | Process of treating an aqueous extract of vegetable origin with biopolymer additive and powder produced by spraying it |
Non-Patent Citations (1)
Title |
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PATENT ABSTRACTS OF JAPAN vol. 2000, no. 14 5 March 2001 (2001-03-05) * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006084658A1 (en) * | 2005-02-10 | 2006-08-17 | Indena S.P.A. | Oral compositions for the prevention of uv damages |
WO2011018579A1 (en) | 2009-08-11 | 2011-02-17 | Totum Bio Cosmetics | Method for preparing whole olive juice, composition produced according to the method, and use thereof in the field of cosmetics and dietetics |
FR2949059A1 (en) * | 2009-08-11 | 2011-02-18 | Raphael Colicci | PROCESS FOR THE PREPARATION OF AN INTEGRAL JUICE OF OLIVE, COMPOSITION OBTAINED ACCORDING TO SAID METHOD AND ITS APPLICATION IN THE FIELD OF COSMETICS AND DIETETICS |
CN102666821A (en) * | 2009-08-11 | 2012-09-12 | 托特姆生物化妆品公司 | Method for preparing whole olive juice, composition produced according to the method, and use thereof in the field of cosmetics and dietetics |
Also Published As
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FR2867071B1 (en) | 2006-06-09 |
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