GB2374284A - Safe, eco-friendly health protective herbal colours and aroma useful for cosmaceutical applications - Google Patents
Safe, eco-friendly health protective herbal colours and aroma useful for cosmaceutical applications Download PDFInfo
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- GB2374284A GB2374284A GB0108033A GB0108033A GB2374284A GB 2374284 A GB2374284 A GB 2374284A GB 0108033 A GB0108033 A GB 0108033A GB 0108033 A GB0108033 A GB 0108033A GB 2374284 A GB2374284 A GB 2374284A
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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
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
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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
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9794—Liliopsida [monocotyledons]
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
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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
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
- A61Q1/06—Lipsticks
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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
- A61Q1/08—Preparations containing skin colorants, e.g. pigments for cheeks, e.g. rouge
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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
- A61Q1/10—Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/42—Colour properties
- A61K2800/43—Pigments; Dyes
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Abstract
A novel safe and eco-friendly health protective and beauty enhancing herbal composition having various cosmetic applications such as lipsticks, eye shadows, glow-glitters and rouges, said composition containing colourants from plants, for example, of the family <I>Boraginaceae</I>, the invention also provides a method for preparing the said composition. The invention also relates the use of lipsticks as a medium of aromatherapy.
Description
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SAFE, ECO-FRIENDLY, HEALTH PROTECTIVE HERBAL COLOURS
AND AROMA USEFUL FOR COSMACEUTICAL APPLICATIONS FIELD OF THE INVENTION
The present invention relates to a safe, eco-friendly, health protective and cosmetic composition useful as lipstick and for other cosmaceutical applications like eye-shadows, skin creams, glow-glitters and rouges.
BACKGROUND AND PRIOR ART
There is worldwide revival of interest in the use of natural colours especially in cosmetics and pharmaceuticals as the synthetic colours are likely to cause many side effects. Keeping this in view the present invention is undertaken to develop purely natural herbal colorants for cosmetic compositions. One aspect of the invention pertains to the development of a herbal composition useful as Lipstick with moodaltering functional attributes including stimulation of creative thoughts on persons who apply the same on lips. Such features of the composition are attributed to the selected blended formulations of Natural colours and essential oils/aroma isolates incorporated.
Lips being-the-most-sensitive part-of skin ;-can effect fast transdermal absorption and also the lips being very close to nose facilitate a continuous inhalation of the slowly vaporizing essential oils/aroma chemicals blended in the composition, thus, providing a double effect on the specific centers of the brain by releasing neurochemicals leading to mood alteration stimulation and change of mental perceptions. The different blends of essential oil/aroma isolates/natural aroma chemical selectively blended in the lipsticks provide anti-depressant, mood enhancing/mood lifting effect and give rise to creative thoughts.
While lipsticks with different colour shades blended with aromatic principles have been developed for women, another range of compositions useful as lipsticks has also been developed for men. These compositions are without colours but provide a moisturizing transparent effect and have mood altering functions and are designed to altered mental perception, functioning similar to the lipstick compositions developed for developed for women. Both the groups of lipstick have some additional health promotive/protective and beautifying attributes by preventing the lips from darkening and providing it with moisturizing effects. These compositions also give attractive luster and texture to the lips. The lipsticks with colour, developed for women, have antibacterial, antifungal and anti-inflammatory effects. With regard to lip beatification topical application
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lipstick with different shades of colours are well known. Likewise, spraying of aromatic oils or sprays for refreshing is also well known. Many studies have been carried out on the effect of fragrance on mental perception ; for example, the nice fragrance has an aesthetic impression and multiple positive effects on our life, they are not only for pleasure and seduction, healing and magic products but also for positive mood creators.
DESCRIPTION OF PRIOR ART
Reference is made to a publication titled''Naphthaquinones of Arnebia Nobilis"by Y. N.
Shukla et al., Phytochemistry, 1971, Vol. 10, pp. 1909 to 1915, wherein, 4-naphthaquinones
designated as A-1, A-2, A-3 and A-4 have been reported. The use of the extract from Arnebia nobilis is also reported. - Sayyada Khatoon and Shanta Mehrotra in"Naphtha quinones from some Boraginaceous Texa-A Chemical Review" published in Natural Product Sciences, 1996 2 (2)-pp. 75-85 report a number of naphthaquinones from boraginaceous plants. Varies properties of these-compounds have also been reported.
V. P. Papageorgiou, has reported certain lipophilic red pigments obtained from various plants
including the genus Lithospermum, Echium Onosma Anchusa and Cynoglossum, in his publication titled : Naturally occurring Isohexenylnaphthazarin Pigments : A New Class of Drugs"in Planta Medica, 1980, Vol. 38, No. 3.
US Patent 4996044 describes a lipstick formulation consisting of organic high staining dyes, said formulation having creamy, shiny and soft laydown and long wear properties. The formulation does not use any extracts from any plant.
Reference is made to a US patent (No. 5593662) wherein moisturizing lipstick has been described. In this invention, use has been made with a composition of 30-80% lipophilic material,
which may have lesser shelf life and may promote microbial growth due to the presence of moisture. They used about 0-35% synthetic colourant which seems to be too high for a cosmetic composition. The synthetic colours mostly exhibit harmful side effects like loss of luster, blackening of skin and may have some carcinogenic effects too as shown in a website (http://www. orst. eduffoodresource/color/colorantsl. html).
Another reference is made to patent no. 5665778 wherein a ceramide, process for their preparation and their application in cosmetics and in dermato-pharmacy. These compounds are complex mixtures of erythro & threo-diasterioisomers. They synthesize these compounds by a
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complex and costly process. They have used organic pigments for lipstick and there is no herbal colourants being used.
Reference may be made to a recent PCT application PCT/EPOO/02217 of 13 March 2000 wherein the inventors have used Zinc salts, particularly Zinc citrate in lipstick to effect antimicrobial property. The drawback in using Zinc or its salts is that mostly they are emetic and cause conjunctivitis as side effect.
In an International Congress of Essential oils, fragrance and flavours (November 1989) the description of use of aroma has not at all been mentioned in lipstick. The available lipsticks in the international market are used as refreshing beautifying agents only.
US Patent 5665778 describes yet another cosmetic formulation consisting of ceramides and other compounds. The composition of this patent is a totally synthetic composition.
US Patent 5676957 describes a skin external agent, said agent being an extract of the plant of genes Euonymus such as Euonymus alata. This extract according to this invention may be
formulated with a costnetically acceptable b. ase. ~ ~ ~ Reference is made to a US patent No. 5, 85, 8348 wherein only a single isolate of essential oil like rose-oxide-has-been used in synthetic lipstick and other cosmetic for refreshing feel. Such a single isolates of essential oil will not serve-the--desired-multiple-effeFcts-Eke mood enhancing, sensual pleasure and thought inducing state of mind.
To the knowledge of the applicants, there does not exist any lipstick with herbal colours and functional attributes, the cosmaceuticals like eye shadows and glow glitters, rouges with use of herbal colours, likewise the lipstick without colour with functional attributes for men.
OBJECTS OF THE INVENTION
The main objective of the present invention is to provide safe, eco-friendly, health protective and cosmetic composition containing natural colours and aroma/essential oils useful for various cosmaceutical applications.
Another objective of the present invention is to use the herbal colours in lipsticks.
Another objective of the present invention is to provide transparent cosmetic compositions useful as lipsticks and containing essential oils/aroma isolates.
Still another objective of the present invention is to use the herbal colours in other cosmetic compositions like eye shadows, skin creams, glow glitters and rouges.
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Yet, another objective of the present invention is to provide the use of the functional lipstick as a means to camouflage leucodermic skin and particularly lips.
Yet another object of the invention is to provide a method for the production of cosmetic compositions containing herbal colourants and useful in other cosmetic applications.
SUMMARY OF THE INVENTION
The invention provides a safe, eco-friendly, health protective and beautifying herbal composition containing colourants and aroma, and useful for various cosmaceutical applications. The invention also provides a process for the preparation of the herbal cosmetic composition comprising extraction of colourants from natural sources such as plants, and mixing the colourants with aroma and other base material for cosmaceutical applications.
DETAILED DESCRIPTION OF THE INVENTION
This invention relates to an herbal cosmetic composition containing colouring agents for - ---------- - -- -- - - topical or external use. More particularly, the invention provides a novel cosmetic composition, useful especially as lipstick. When used as lipstick, the composition contains herbal colourants for which is then blended-with-selected-blends of essential oils-or aroma isolates and the composition is capable of altering the mood and mental perception of the person, who applies it.
A safe ecg. mendly, health protective and beautifying herbal cosmetic composition containing herbal colourants together with a cosmetically acceptable amount of one or more additives providing special properties and a cosmetically acceptable base material.
Accordingly the present invention provides a composition comprising additives providing special properties are selected from essential oils/aroma isolates obtained from the group of plant species belonging to genera Acquillaria, Cinnamomum, Cymbopogon Elettaria, Eucalyptus, Geranium, Jasminum, Ocimum, Pelargonium, Rosa, Rosmarinus, Santalum and Vetiveria.
In one embodiment of the invention, the essential oils/aroma isolates act as mood lifting agents, antidepressant agents, anti stress agents, sensual pleasure providing agents, creative thought inducing agents, anxiety reducing agent, refreshing agent, stimulant, soothing agents, anti oxidants, fixative, fragrants, and antimicrobial.
The applicants have found that the herbal colourants are obtained from various plants of the family Boragznaceae. It is the finding of the applicants that a wide spectrum of colors can be obtained from the said plants by using specific solvents in specific proportions. For instance, petroleum ether and chloroform may successfully be used m different proportions for extraction of
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the colored matter from the said plants in order to achieve a wide spectrum of colors such as pastel red, purplish red, cerise, ruby red, deep magenta, beet root purple, amarynth, dark purple, dark violet, deep violet, deep blue blackish blue, etc. It is pertinent to note that each of the plants listed above are capable of yielding the above spectrum of colors.
The applicants have found that the herbal colorants obtained from various plants together with the essential oil and conventional additives yield a herbal composition which is suitable for cosmetic applications such as lipsticks.. This herbal composition is devoid of toxic effects. The applicants also believe that the essential oils and aroma isolates may have the properties of mood enhancement, sensual pleasure, antidepressant and creative thought inducer. Also, the essential oils and aroma isolates may be used in transparent lipstick as a functional attribute.
The proportion in which the coloring matter/coloring compounds can be mixed with essential oils and additives can be readily determined by a person skilled in the art. However, it is preferred that 0.0005% of coloring matter may be-mixed with l04 % essential oil, 1% lustering agent such as safEloweroilT'The base and other matters'added may make up 100%.
Herbal lipophilic, safe colours are extracted from the plants belonging to the genus
Arnebia, Bixa, Butea, Carthamus, Hibiscus, Jatropha, Lithospermum, Macrotomia, Maharanga, - -- ---- -""'--- - -- ---Nyctanthes, Onosma, Rhododendron, and Tagetes which are known to be non toxic and free from any strong side effects on human body particularly on topical application. The colours extracted from these plants are bright and lustrous and have pronounced antibacterial and anti-inflammatory activities. For example a good bright colourant-red-andora colour, plate No. 8.4 L of Dictionary of colours (Maerz and Paul, 1950) and after applying on lips, pomegranate to Vemonia purple (plate 6.3 L-6. 5 A of the same dictionary provides different functional effects such as mood refreshing, concentration enhancing, CNS relaxant, accelerating working rate and improves capacity to work. It is pertinent to note that each of the plants listed herein is capable of yielding a wide spectrum of colours.
Accordingly, the present invention provides safe, eco-friendly, health protective herbal colours and aroma useful for cosmaceutical applications which comprises safe, eco-friendly, health protective and beautifying herbal colourants and aroma useful for cosmaceutical applications, comprising extraction of organic compounds from natural sources such as plants, the said extracted organic compounds being used as a colourant with aroma in base material for cosmaceutical applications.
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An embodiment of present invention is that the safe herbal colourants may be isolated from different plant species belonging to the genera of family Boraginaceae which are non-toxic and may be free from any side effects.
Another embodiment of present invention is that the aroma isolates/essential oils may be selected from group of plants - Aquillaria, Cinnamomum, Cymbopogon, Elettaria, Eucalyptus, Geranium, Pelargonium, Rosa, Rosamarinus, Santalum and Vetiveria.
In other embodiment, the herbal colourants may be used in lipsticks, eye shadows, glow glitters and rouges.
In still other embodiment the lipstick containing essential oils and combinations of aroma isolates may release neurochemicals in the brain through the receptors in mouth and nose and may have the properties of mood enhancement, sensual pleasure, antidepressant and creative thought inducer.
# In yet another embodiment of the invention, the anti-depressant property imparted by the essential oils are selected from
Essential Oils Preferred Ratio 1. Ocimum oiL'Jasminum oil : Cymbopogon oil (1 : 2 : 1) 2. Ocimum oil : Mentha oil: Rosmarinus oil (2 : 1 : 1) 3. Jasminum oil : Mentha oil : Rosmarinus oil (1 1 4. Cymbopogon oil: Ocimum oil: Mentha oil (1 : 2 : 1) 5. Ocimum oil: Cymbopogon oil (2 : 1) 6. Mentha oil : Rosmarinus oil 7 Ocimum oil 8. Rosmarinus oil In yet another embodiment of the invention, the creative thought-inducing property is, imparted by the essential oils selected from
Essential oil Preferred ratio 1. Santaium oil 2. Santalum oil: Rosa oil (1 : 2) In yet another embodiment of the invention, the anti-stress property is imparted by the essential oils selected from
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Essential oil Preferred ratio 1. Santalum oil: Lavandula oil (2 : 1) 2.Lavandula oil: Eucalyptus oil: Rosa oil (1 : 1 : 1) 3. Eucalyptus oil: Rosa oil (1 : 2) 4. Aquillaria oil: Elettaria oil: Rosmarinus oil (1 : 1 : 1) 5. Jasminum oil 6 Santalum oil 7. Lavandula oil In yet another embodiment of the invention, the refreshing property is imparted by the essential oils selected from
Essential oil Preferred ratio 1. Santalum oil : Rosa oil : Rosmarinus oil (1 : 1 : 1) 2. Santalum oil : Pelargonium oil (1: 2) 3 Jasminum oil: Lavandula oil (1 : 2) 5 Lavandula oil 6 Santalum oil : Oa oi/ 6 Santulam oil In yet another embodiment of the invention, the sensual feeling property is imparted by the essential oils selected from
Essential oil Preferred ratio 1. Jasminum oil : Lavandula oil : Pelorgonium oil (1: 2) 2. Ocimum oil: Jasminum oil : Cymbopogon oil (1 : 2: 1) 3. Jasminum oil 4. Jasminum oil: Lavandula oil (2: 1) In yet another embodiment of the invention, the mood lifting property is imparted by the essential oils selected from
Essential oil Preferred ratio 1. Jasminum oil : Rosa oil : Palergonium oil (1: 2) 2. Rosmarinus oil (1 : 2) 3. Cymbopogan oil: Rosa oil (2: 1) 4. Rosa oil 5. Jasminum oil : Rosa oil In yet another embodiment of the invention, the anxiety reducing property is imparted by the essential oils selected from
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Essential oil Preferred ratio 1 Rosa oil: Cinnamomum oil (1: 2)
Still another embodiment of the invention is that the essential oils and aroma isolates are used in transparent lipstick as a functional attribute.
Still another embodiment of the invention relates to the composition wherein, tocopherol is used as an antioxidant, which also functions as fixative, and may be present in traces to ppm.
An embodiment is that the process for extraction of organic compounds from natural sources such as plants which comprises drying of plant parts, powdering by known means, the said dried powder being used to extract herbal colourants, optionally treating the said colours with acids or bases taken in different proportions, to produce various shades.
Yet another embodiment, the plant parts may be root, stem, leaf, and the quantum of essential oils used in preparing compositions vanes based on the part from which the oil is
- ------ - extracted.
Still another embodiment of the present invention is that the plant parts may be dried at a temperature in the range of 3045 C, n sha-de ~ ~ An another embodiment the dried plant parts may be powdered to particles of the size in the range of 30-60 mesh.
Further embodiment, the herbal red colourants may be extracted from the plants of the genera Arnebia, Bixa, Butea, Carthamus, Hibiscza, Jatropha, Lithosper ? num, Macrotomia, Maharanga, Nyctanthes, Onosma, Rhododendron, and Tagetes. The plants or their parts are put in a Soxhlet apparatus at a temperature of 20-800C. The solvents selected for the extraction may be nonpolar-hexane, petroleum ether, toluene and cyclohexane, wherein the polar solvents are selected from chloroform, acetone, ethyl alcohol and methyl alcohol. The non-polar and polar solvents may be recovered at reduced pressure of 50-100 psi and a temperature of 40-800C. The herbal colourants are obtained after the recovery of the solvents. The concentrates result colours of various shades such as purplish red, cerise, ruby red, beetroot purple, dark violet, deep blue, and blackish blue colours which are herbal in nature as no trace of organic solvent remains in the final concentrate.
Further, the present invention provides a process for preparation of herbal colourants, which comprises the steps of drying the plant material, powdering the same and percolating it with ethyl or methyl alcohol at a temperature of 20-480C. The alcohol soluble matter is concentrated at reduced
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pressure of 50-100 psi and a low temperature of 40-60oC. The concentrate is eluted with silica gel column chromatography using non-polar solvents like-petroleum ether, hexane, cyclohexane, toluene and a mixture of non-polar and polar solvents. The polar solvents used may be like chloroform, acetone, ethylacetate and methanol. The ratio of the non-polar and polar solvents may be 20: 1 to 4: 1. The concentration of the column fractions may be made at a range of reduced pressure of 80-100 psi and a temperature of 30-60oC. The colours of the concentrate may be pastel red, pale red, purplish red, rose red, cerise, ruby red, deep magenta, beetroot purple, amaranth, dark purple, dark violet, deep violet, deep blue and blackish blue
In still another embodiment the herbal colourants may be antimicrobial, anti-inflammatory and may be used in leucoderma, more particularly of lips.
The embodiment of the present invention the herbal colourants may be the mixture of naphthazarins and may be cyclic unsaturated diketones in which double bonds and keto group may be conjugated.
The another embodiment of present invention the herbal colourants may be changed in different shades with organic and inorganic acids. The intensity of colours may be increased with
"orgaaic acids-and may be decreased with morganiccidsrTne'anger of the concentration of the acids may be 0.1-10%.
Still another embodiment of the invention that the herbal colours may be changed with organic and inorganic bases.
Another embodiment of the present invention the base concentration may be in the range of 0.1 to 20%.
Yet another embodiment the herbal colour may be lipophilic and hydrophilic properties may be very minimllII1.
Still another embodiment the herbal colours may be soluble in organic solvents likehexane, petroleum ether, benzene, diethyl ether, ethylacetate, chloroform, acetone and alcohol in the range of 30-100%.
In an embodiment, the pH of the extracted herbal colours may be 5-6.
The present invention is aimed to prepare safe, eco-friendly, health protective herbal colours and aroma useful for cosmaceutical applications which comprises extraction of organic compounds
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from natural sources, the said extracted organic compounds being used as a colourant with aroma in base material for cosmaceutical applications.
The safe herbal colourants may be isolated from different plant species belonging to the genera of the family Boraginaceae which are non-toxic and may be free from any side effects.
The present invention is that the aroma isolates/essential oils may be selected from group of plants-Aquillaria, Cinnamomum, Cymbopogon, Elettaria, Eucalyptus, Geranium, Pelargonium, Rosa, Rosamarznus, Santalum and Vetiveria. The herbal colourants may be used in lipsticks, eye shadows, glow glitters and rouges.
The lipstick containing essential oils and combinations of aroma isolates may release neurochemicals in the brain through the receptors in mouth and nose and may have the properties of mood enhancement, sensual pleasure, antidepressant and creative thought inducer.
The invention is that the essential oils and aroma isolates may be used in transparent lipstick - -------- - - as a functional attribute.
Another aspect of the invention relates to a process for extraction of organic colourants from the plants, said process comprising obtaining the plant parts, extracting with organic solvents, removing the solvents by conventional methods, concentrating the extract under reduced pressure and optionally treating with acids or bases to produce various shades.
Yet another aspect of the invention relates to a process for the extraction of organic colourants, said process comprising the steps of : a) drying the plant parts, b) powdering the dried plant parts, c) subjecting the dry powder obtained in step (b) to Soxhlet extraction at a temperature in the range of 40-80 C or cold percolation with organic solvents at a temperature ranging between 20 to 45 C, d) concentrating the mixture of step (c) by conventional methods at reduced pressure in the range of 50-100 psi and at a temperature not exceeding 50 C, e) mixing the concentrate of step (d) with silica gel in the ratio 1: 3 to 2: 7 to obtain a slurry, f) eluting the slurry with organic solvents resulting in various fractions, g) concentrating the fractions at a pressure in the range of 50-100 psi resulting in herbal colourants, optionally treating the said colours with acids or bases to produce various shades, and
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h) obtaining various colours from by treating the said fractions with acids or bases to produce colourants of various shades.
One more aspect of the invention relates yet another process of extraction of herbal colourants from plants of the family Boraginaceae, which comprises; percolating powdered plant parts with alcohol at room temperature resulting in alcohol soluble herbal material, the said herbal material being concentrated by known means at pressures in the range of 50-100 psi and at a temperature in the range of40-60 C, the said concentrate being made into a slurry with silica gel in a ratio in the range of 1: 3 to 2: 7, the said slurry being eluted by known means with organic solvents resulting in fractions, the said : fractions further being concentrated by known methods at a pressure in the range of 50-100 PSI resulting in herbal colorants, optionally treating the said colours with acids or bases to produce various shades.
The herbal colours may be extracted from any of the three parts of the plants; namely root, stem or leaves or by taking all of them. These parts may then dried by any conventional means
- ----- - --- - which may include heat treatment at a temperature between 30-45 C. Alternatively the drying process may be effected in shade though the time for drying may be rather too long. The dried plant material may-then-be-powdered and sieved-through mesh-to-get-a powder of particles of a suitable size preferably in the range of 30-60 mesh
The-dried powder may then be extracted by using Soxhlet apparatus at a temperature range of 40-80oC.
The dried powdered plant material may also be extracted by cold percolation at a temperature range of 20-45oC.
The extraction may be carried out with the non-polar and mixtures of non-polar and polar solvents selected for the extraction. Non-polar solvents may be selected from hexane, petroleum ether, toluene and cyclohexane whereas the polar solvents may be selected from chloroform, acetone, ethyl alcohol and methyl alcohol. The herbal colours may be obtained by concentrating the extracts at reduced pressure of 50-100 psi and a temperature at range of 40-60 C. This process of concentration may result in purplish red, cerise, ruby red, beet root purple, dark violet, deep blue, and blackish blue colours which are herbal in nature as no trace of organic solvent remains in the final concentrate.
In another process, the dried, powdered plant material may be percolated with ethyl or methyl alcohol at a temperature of 20-48oC. The alcohol soluble matter may be concentrated at
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reduced pressure of 50-100 psi and a low temperature of 40-60oC. Thus, the said concentrate may be eluted with silica gel column chromatography by using non-polar solvents like-petroleum ether, hexane, cyclohexane, toluene and mixture of said non-polar and polar solvents. The polar solvents may be used like-chloroform, acetone, ethylacetate & methanol. The ratio of the non-polar and polar solvents may be 20: 1 to 4: 1. The concentration of the column fractions may be made at a range of reduced pressure of 80-100 psi and a temperature of 30-60 C. The colours of the concentrate may be pastel red, pale red, purplish red, rose red, cerise, ruby red, deep magenta, beet root purple, amaranth, dark purple, dark violet, deep violet, deep blue and blackish blue
These novel colours may be used with or without the aroma isolate/essential oils. Proper mixture of aroma isolates/essential oils may result in such desirable properties of mood enhancement, sensual pleasure, antidepressant and-creative thoughts inducer To get these desired properties in cosmetics like lipsticks the herbal colours may be mixed with selected mixture of aroma and applied to the base material. These herbal colours may be used in other applications like eye shadow, glow-glitters, rouges and-skin-conditioning agent.
These colours may be the mixture of naphthazarins and may be cyclic unsaturated diketones in which double bonds, and keto group may be conjugated. These herbal colours may be changed to different shades by treating it with organic and inorganic acids. The intensity of these colours may be increased with organic acids and may be decreased with inorganic acids. The range of the concentration of the acids may be 0.1-10%. The colour of the herbal colourants may be changed from red to blue with organic and inorganic bases. The range of the concentration of the bases may be 0.1-20%.
These herbal colours may have excellent lipophilic properties and very minimum hydrophilic properties. These colours may be soluble in organic solvents like-hexane, petroleum ether, benzene, diethyl ether, ethylacetate, chloroform, acetone and alcohol in the range of 30- 100%. The pH of the extracted colours may be within the range of 5-6. All these characteristics of the herbal colours are very desirable for use in cosmaceutical applications. The process of the present invention can obtain various colours such as described in the tables 3 to 6.
Some of the critical parameters, which are responsible for the generation of various colourants, are as under: a) composition of the solvent used for runmng the column chromatography.
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b) the ratio of the polar to non-polar solvent is also a critical parameter for the production of the different colours. c) the temperature of the Rotavapours used in the process of the concentration of the extract is also a critical parameter. d) the temperature of the hot air oven at which the lipstick formulation is made is also a critical parameter. e) treating the said colours with specific concentration of acids or bases to produce various shades.
Novel features of the invention: 1. Extraction of the herbal colours from plant materials which are non-toxic and highly lipophilic.
2. A novelty of the present invention lies in application of herbal colours in cosmaceutical preparationshkeJJLpsticks, eye shadows-glow glitters and rouges.
3. Ability to tailor the shade of the basic herbal colours by a simple treatment of the produce with organic or inorganic acids or bases.
Brief description of the drawings.
Thus, the process of the invention can be used to achieve different colourants. Some of the colourants obtained are shown in the accompanying drawings. In the accompanying drawings: Fig 1 represents colourant of red-purple group (60C) Fig 2 represents colourant of red-purple group (61A) Fig 3 represents colourant of red-purple group (58A) Fig 4 represents colourant of red-purple group (46A) Fig 5 represents colourant of red-purple group (53A) Fig 6 represents colourant of blue group (103A) Fig 7 represents colourant of blue group (99A)
Fig 8 represents colourant of orange group (25B) Fig 9 represents colourant of orange red group (31 C) Fig 10 represents colourant of orange red group (34C)
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Fig 11 represents colourant of orange red group (32C) Fig 12 represents colourant of orange red group (33B) Fig 13 represents colourant of red group (46A) Fig 14 represents colourant of red group (44A) Fig 15 represents colourant of red group (46B) Fig 16 represents colourant of red group (59A) Fig 17 represents colourant of blue group (103B) Fig 18 represents colourant of blue group (103A) Fig 19 represents colourant of blue-green group (1 14A) Fig 20 represents colourant of greyed-purple group (187B) Fig 21 represents colourant of greyed-purple'grdup (187A) Fig 22 represents colourant of purple group (79A) Fig23represents colourantTof brown-group- (200A) Fig 24 depicts a few of various shades of lipsticks obtained according to the invention.
Brief description of the tables.
Table 1 depicts preferred list of Aroma i. e. essential oils for the functional attributes in cosmaceutical application Table 2 represents preferred list of Aroma isolates for the functional attributes in cosmaceutical application Table 3 represents change of colours obtained from direct extraction (process 1)-Change of colours with bases Table 4 represents change of colours obtained from direct extraction (process 1)-Change of colours with acids Table 5 represents change of colours obtained from column (process 2)-Change of colour with acids Table 6 represents change of colours obtained from column (process 2)-Change of colour with bases.
Table 7: Table for correspondence of colour codes based on Flower Council of Holland.
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The various colours shown are codified according to RHS colour chart in associatiation with Flower
Council of Holland and The Royal Horticultural Society, London.
The following examples are given to illustrate the invention and should not be construed to limit the scope of the present invention.
PREPARATION OF HERBAL COLOURANTS AND LIPSTICK:
The present invention is illustrated further by referring to the following examples.
However, the present invention is not limited to these examples.
Process Extracted the powdered material with non-polar solvents (like hexane, petroleum ether, toluene and cyclohexane) and mixtures of non-polar and polar solvents (The polar solvents are chloroform Acetone, Ethylacetate, methanol, ethanol).
The ranges of ratio of non-polar and polar solvents are 99: 1 to 0: 100.
The change of color by treating the color with traces of food grade acids e. g. Acetic acids less than 0.1% The change of color with the treatment of traces of bases i. e. less than 0. 1%.
Example - 1 100 gm air-dried coarsely powdered root of Onosma species is sieved in 40 mesh sieve and then extracted in Soxhlet apparatus with hexane at a temperature of 500C for 12-18 hours which resulted in the formation of hexane soluble herbal matter. The said matter was concentrated at a reduced pressure of 70 psi and at a temperature of 3SoC, resulting in the yield of 6.0 gm. as the purplish red colour (Plate NO 12 A7 of Methuen handbook of colour, 1978).
Example-2
100 gm air dried coarsely powdered stem and root in the ratio of 1: 4 of Onosma species is sieved in 40 mesh sieve and then extracted in Soxhlet apparatus, with chloroform, at a temperature of 60 C for 18-24 hours which resulted in the formation of chloroform soluble herbal matter. The said matter was concentrated at a reduced pressure of 80 psi and at the temperature of 40 C, resulting in the yield of 8. 5 gm. as the beet-root purple (Plate No: 13 D8)
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Example-3
100 gm air dried coarsely powder stem, root and leaf in the ratio of 1: 1: 3 of Macrotomia species is percolated at room temperature with the mixture of chloroform and hexane in the ratio of 5: 95 for 4 hours (3 times). Combined all the extracts and concentrated at a pressure of 70psi and a temperature of 50oC. Thus 3.5 gm of cerise colourant (Plate No: 12 C8) was obtained.
Example-4
100 gm air-dried coarsely powdered root of Onosma species is sieved in 40 mesh sieve and then extracted in Soxhlet apparatus with hexane at a temperature of 50 C for 12-18 hours which resulted in the formation of hexane soluble herbal matter. The said matter was concentrated at a reduced pressure of 70 psi and at a temperature of 35 C, resulting in the yield of 6.0 gm. as the purplish red colour (Plate NO 12 A7) which gets changed to rose red after treatment with 1% formic acid
Example-5
100 gm air dried coarsely powdered stem and root in the ratio of 1: 4 of Onosma species is sieved in 40 mesh sieve and then extracted in Soxhlet apparatus, with chloroform, at a temperature of 60 C for 18-24 hours which resulted in the-formation of chloroform-soluble herbal matter. The said matter was concentrated at a reduced pressure of 80 psi and at the temperature of 40oC, resulting in the yield of 8.5 gm. as the beet-root purple (Plate No: 13 D8) which gets changed with 0. 1% HC1 to ruby red colour (Plate No: 12 D8).
Example-6
100 gm air dried coarsely powder stem, root and leaf in the ratio of 1: 1: 3 of Macrotomia species is percolated at room temperature with the mixture of chloroform and hexane in the ratio of 5: 95 for 4 hours (3 times). Combined all the extracts and concentrated at a pressure of 70 psi and a temperature of 50 C. Thus 3.5 gm of cerise colour (Plate No: 12 C8) was obtained which gets changed to vivid blue (Plate No: 21 A8) with the addition of the 0. 1% NaO
Example-7
100 gm air dried coarsely powdered root of Onosma species is percolated with ethyl alcohol at room temperature for 24 hours (4 times). The alcohol soluble portion of stem and root was concentrated at reduced pressure of 70 psi and at a temperature of 50 C, resulting in the formation of 18 gm. of ethanol soluble concentrate. The said concentrate was mixed with 54 gm of silica gel for preparing slurry. This slurry was dried with the help of vacuum pump. The column
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chromatography of this dried slurry was carried out by using hexane: chloroform in the ratio of 95: 5. The fractions obtained with aforesaid solvents were concentrated at the reduced pressure of 90 psi and at a temperature of 40oC, thereby giving the yield of 0.3 gm as the pastel red colour (Plate No: 9 A5) which gets changed to vivid blue (Plate No: 21 A8) with the addition of the 0. 1% NaOH.
Preparation of cosmetic compositions
The herbal colourant obtained by the process described in Examples 1 to 7 can be used according to the invention to develop various cosmetic compositions useful as lip stick, eye-liners, eye-shadows, glow-glitters and rouges. Such compositions are prepared following the general principles used in making cosmetic compositions. Specifically, the herbal colourant obtained from the plant parts is mixed with a base in appropriate proportion. The base may be liquefied first and the colourant of choice may be added and stirred. Alternatively, the colourant and the base are added, the mixture is heated, and the ingredients are stirred to obtain a homogenous mixture. To this mixture, essential oil is added together with softening agents, mood lifting agents and other
- ---- - ----- - - --additives as may be necessary for the compositions. For instance, if glow-glitters composition is to be prepared, with the basic composition, additives that provide glitter are added. The composition prepared when cooledto, room temperaturcbecomes suitable for use as a cosmetic composition.
! While the above is only an outline describing the preparation of cosmetic composition, specific instances of preparing different cosmetic compositions for various applications is described in Examples 10 to 17 here below. The specific instances provided herein below are meant only to illustrate the invention and the same should not be construed to limit the scope of the invention in any manner.
Example-8
0.5 mg of herbal colour was mixed with I ml of Safflower oil and I ml Castor oil thoroughly. In the said mixture 1. 5 gm of melted bees wax was mixed at a temperature of 70 C. After that 5 microlitre tocopherol and 1 microlitre of Rosamarinus essential oil was added to the aforesaid mixture. Then the mixture was cooled to room temperature. This cooled mixture is now ready for application.
Substance Amount Percentage 1. Colour 0. 5mg 0. 5%
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2. Safflower oil 1. 0mi 1.0% 3. Castor oil 1. O ml 1.0% 4. Tocopherol 5 Al 0.005% 5. Rosamarinus (Essential oil) 1. 0). 11 0. 001% 6.Bees wax 1.5 gm To make up 100%
Example-9 0.5 mg of herbal colour was mixed with 1 ml of Safflower oil and 1 ml Castor oil thoroughly. In the said mixture 1.5 gm of melted bees wax was mixed at a temperature of 70 C. After that 5 microlitre tocopherol and 1 microlitre each of Jasminum and Santalum essential oils were added to the aforesaid mixture. Then the mixture was cooled at room temperature. This cooled mixture is now ready for application.
Substance Amount Percentage 1. Colour 0. 1 mg 0.5% 2. Safflower oil 1. 0 ml 1.0% 3. Castor oil 1.0 ml 1.0% 4. Tocopherol 5.0 l 0.005% 5. Jasminum and Santalum 1.0 l 0.001% (Essential oil) 6. Bees wax 1. 5 To makeu 100% Example-10 0.5 mg of red colourant was mixed with 1 ml of safflower oil and 1 ml of castor oil thoroughly. In the said mix, 0.5 gm of melted bees was mixed at a temperature of 70oC. After that 5 microliter tocopheral and 1 microlitre of sandal wood oil was added to the aforesaid mixture. Then the mixture was cooled to room temperature. Thus, cooled mixture is ready for application as eye shadows.
Substance Amount Percentage 1. Colour 0. 5mg 0.5% 2. Safflower oil 1. 0 ml 1.0% 3. Castor oil 1. 0 ml 1.0% 4. Tocopherol 5.0 jl 0. 005% 5. Sandal wood oil (Essential oil) 1. 0 il0. 001%
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6. Bees wax0. 5 gmTo make up 100%
Example-11
1.0 mg of herbal colour was mixed with 1 ml of safflower oil and 1 ml of castor oil thoroughly. Then mixed 0.2 gm of melted bees wax at a temperature of 70 C. After that 10 microliter tocopherol and 2 microlitre of Rose oil was added to the aforesaid mixture. Then the mixture was cooled to room temperature. Thus, cooled mixture is ready for application as glowglitters.
Substance Amount Percentage 1. Colour 1. 0 mg 1.0% 2. Safflower oil 1. 0ml 1.0% 3. Castor oil 1. 0ml 1.0% 4. Tocopherol 10 l 0.01% 5. Rose-oit (Essentialoil)--2 : 0-1 0. 002% 6. Bees wax 0. 2 To make u 100% Example-12- 0.25 mg of rose red colourant was mixed with 10 gm talc in ball mill. In said mixture 1 microliter of Jasmine essential oil was added and mixed thoroughly. The colorant mixed is now ready for rouges.
Substance Amount Percentage 1. Colour 0. 25 mg 0.25% 2. Jasmine (Essential oil) 1.0 Al 0. 001% 3. Talc 10. 0 gm To make up 100%
I Example-13 (Antidepressant activity)
0.5 mg of herbal colour was mixed with 1 ml of Safflower oil and 1 ml Castor oil thoroughly. In the said mixture 1.5 gm of melted bees wax was mixed at a temperature of 70 C. After that 5 microlitre tocopherol and 1 microlitre blend of sweet basil oil (having linaloal and linolyl acetate), Jasminum and lemon grass oil/citral essential oil was added to the aforesaid mixture. Then the mixture was cooled to room temperature. This cooled mixture is now ready for application.
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Substance Amount Percentage 1. Colour 1. 5mg 1.0% 2. Safflower oil 1. 0 ml 1.0% 3. Castor oil 1. 0 ml 1.0% 4. Tocopherol 10. gel 0. 01% 5. Sweet basil oil, Jasmine and lemon 2. 0pu 0. 002% grass oil 6. Bees wax 1.5 gm To make up 100%
Example-14 (Mood lifting)
1.5 mg of herbal colour was mixed with 1 ml of Safilower oil and 1 ml Castor oil thoroughly. In the said mixture 1.5 gm of melted bees wax was mixed at a temperature of 70 C. After that 5 microlitre tocopherol and 1 microlitre blend of Jasmine, Muskon oil and lavender oil essential oil was added to the aforesaid mixture. Then the mixture was cooled to room temperature. This cooled mixture is now ready for-application
. Substance Amount Percentage 1.Colour 1.5 mg 1.0% 2. Safflower oil 1.0ml 1.0% 3. Castor oil 1.0 ml 1.0% 4. Tocopherol 10 Al 0.01% 5. Jasmine, Muskon oil and 2. 0 gel 0. 002% Lavender oil (Essential oil) 6. Bees wax 1. 5 To make u 100%
Example - 15 (lipstick for men)
1 ml of Safflower oil and 1 ml Castor oil thoroughly. In the said mixture 1.5 gm of melted bees wax was mixed at a temperature of 70 C. After that 5 microlitre tocopherol and 1 microlitre blend of sandal wood oil'and basil oil was added to the aforesaid mixture. Then the mixture was cooled to room temperature. This cooled mixture is now ready for application.
Substance Amount Percentage 1. Safflower oil 1.0 ml 1. 0% 2. Castor oil 1. 0 ml 1.0% 3. Tocopherol1010. 01%
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4. Sandal wood oil or basil oil 2. 0 l 0.002% (Essential oil) 5. Bees wax 1. 5 To make u 100% Table 1: Preferred list of Aroma i. e essential oils for the functional attributes in cosmaceutical application
FUNCTIONAL ESSENTIAL OILS PREFERRED RATIO ATTRIBUTES 1. Antidepressant 1. Ocimum oil : Jasminum oil : Cymbopogon oil (1 : 2 : 1) 2. Ocimum oil : Mentha oil: Rosmarinus oil (2 : 1 : 1) 3. Jasminum oil: Mentha oil: Rosmarinus oil (1 : 1 : 1) 4. Cymbopogon oil : Ocimum oil : Mentha oil (1 : 2 : 1) 5. Ocimum oil: Cymbopogon oil1 (2 : 1) 6. Mentha oil : Rosmarinus oil (1 : 1) 7 Ocimum oil 8 Rosmarinus oil 2. Anti stress 1. Santalum oil: Lavandula-oil (2 : 1) 2. Lavandula oil : Eucalyptusoil : Rosa oil (1 : 1 : 1) 3. Eucalyptus : l : Rosa oil (1 : 2) 4. Aluillaria oil: Elettaria oil: Rosmarinus oil (1 : 1 : 1) 5. Jasminum oil 6. Tantalum oit 7. Lavandula oil 3. Refreshing 1. Santalum : Rosa oil: Rosmarinus oil (1 : 1 : 1) 2. Santalum oil : Pelargonium oil (1 : 2) 3 Jasminum oil: Lavandula oil (1 : 2) 4 Lavandula oil 5 Santalum oil : Rosa oil (1 : 2) 6 Santulam oil 4. Sensual Feeling 1. Jasminum oil : Lavandula oil : Pelorgonium oil (1 : 2: 1) 2 Ocimum oil: Jasminum oil: Cymbopogon oil (1 : 2 : 1) 3 Jasminum oil 4 Jasminum oil: Lavandula oil (2 : 1) 5. Creative Thoughts 1. Santalum oil 2 Santalum oil: Rosa oil (1 : 2) 6. Mood lifting 1. Jasminum oil: Rosa oil: Palergonium oil (1 : 2) 2. Rosmarinus oil 3. Cymbopogan oil : Rosa oil (2 : 1) 4. Rosa oil 5 Jasminum oil : Rosa oil 7. Anxiety 1. Rosa oil : Cinnamomum oil (1 : 2)
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Table 2: Preferred list of Aroma isolates for the functional attributes in cosmaceutical application.
FUNCTIONAL AROMA ISOLATE PREFERRED RATIO ATTRIBUTES 1. Anti stress Citral 2. Refreshing 1. Linalol 2. Benzyl alcohol 3. Terpeneol 4. Terpeneol : Linalol (1:2) 3. Sensual Feeling BMnc ac d 4. Creative Thoughts 1. Isobutyric acid: Butyric acid: linalol (1:2:1) 2. Isobutyruc acud: Benzyl: linalol (1:2:1) 3. Isobutyr acid : 4. Linalol: Isobutyric acid (1:2) 5. Mood lifting 1. Jasmone 2. Citral 3. Eugenol 4. Citral 5. Eugenol: Citral (1:2)
The change in color of the colourants, occurs then they are subjected to acid or base treatments. For example, change of colour occurs by treating the colourant with traces of food grade acids example acetic acid at a quantum less than 0. 1%, likewise, the change of colour occurs with the treatment of base which can be as traces as less than 0. 1%.
The following four tables provide information about the color changes change occur due to acid or base treatments.
Table 3: DIRECT EXTRACTION (PROCESS 1) Change of colour with bases
Sodium Hydroxide Potassium Hydroxide Sodium acetate Code Colours 2% 0.1% 0.05% 2% 0.1% 0.05% 2% 0.1% 0.05% 1. 58C 95A 98B 98B 98B 99C 100B 80D 97B 97C 2. 55A 101A 100D 100B 105D 94B 93D 82A 97C 97D 3. 58B IOIB 100B 100D 101D 93B 93C 80C 97B 97D 4. 55B 9SB 97D 100C 107A 99C 100B 80D 97C 97D 5. 55C 98A 98C 98D 101B 92B 92D 80B 97D 97D 6. 115B 115B 114B 94C 115A 114B 95D 201B 97D 114D
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7. 115A 115A 113C 113C 114D 113C 115B 116B 111B 113C 8. 122A 122A 187B 187C 122B 187C 200D 201A 183C 182A
Table 4 : DIRECT EXTRACTION (PROCESS 1) Change of colour with acids
Acetic acid Citric acid Oxalic acid Code Colours 2% 0. 1% 0.05 2% 0. 1% O. Q5 2% 0. 1% 0. 05 % % % 1. 58C 46C 73B 65B 46B 5"5B 56A 47D 48D 49A 2. 55A 55C 68C 69A 51A 55C 56A 51B 52C 52D 3. 58B 73D 75D 75D 73C 38A 39C 73A 69A 69A 4. 55B 73B 73D 73D 73C 73D 69A 73A 69B 69B 555C 70D 68D 69A 73D 69A 69B 68D 38A 38B 6. 115B 95C 94B 94C 96B 95C 95D 97B 97D 97D 7. 115A 115B 113C 133C 116C 115A 115B 113A 111B 111B 8. 122A 200A 200C 200C 200B 200C 200D 183D 183C 182A Table 5: From Column (PROCESS 2) Change of colour with acids
Acetic acid Citric acid Oxalic acid Code Colours 2% 0.1% 0.05% 2% 0.1% 0.05% 2% 0.1% 0.05% C1 25B 25C 24A 24A 24A 24A 24C 24C 24A 24C 24C 24A C2 31C 29B 29C 29C 27A 27B 27B 29B 29C 27B C334C 33A 33C 33C 33A 33C 33D 33A 33C 33C C4 32C 29A 28C 28D 29A 28D 28D 29A 28C 28D Cs 33B 40C 39C 39D 31B 30C 30D 31C 31D 31D C6 46A 46A 45C 45D 32A 31B 30C 33B 32A 32B C7 44A 43A 40B 40C 45D 42A 42B 45C 44B 44C Cs 46B 47B 47D 47D 47B 48A 48B 46C 46A 46D C9 59A 60A 59D 57D 59B 59D 59D 60B 60C 59C Clo 95A 95C 94B 94C 96B 95C 95D 97B 97D 97D C11 103A 200A 200C 200C 187A 187C 187D 187A 187C 187C Cn 114A 115B 113C 113C 116C 115A 115B 113A 111B IIIB C13 187B 182A 180C 180D 182C 181D 181D 180B 181C 181D C14 187A 59A 60B 60C 59B 58A 58C 59D 58D 58C C15 79A 187A 183A 183C 187B 187B 185C 182C 181D 181D Ci6 200A 200A 200C 200C 200B 200C 200D 183D 183C I82A
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Table 6: From Column (PROCESS 2) Change of colour with bases
NaOH KOH CH3COON2 cOLOURS 2% 0.1% 0. 05% 2% 0. 1% 0.05% 2% 0. 1% 0. 05% Cl 25B 90A 89A 24A 92A 89C 24C 181B 24C 89D C2 31C 106B 106D 29C 98B 105d 27B 58C 29C 105D C3 34C 86C 33C 33C 83B 83C 33D 171C 33C 83D C4 32C 93B 93D 28D 102A 99C 28D 169C 28C 93C Cs 33B 98B 98C 39D 105C 98C 30D 169B 31D 99C C6 46A I03C 102C 45D 98B 102D 30C 34B 32A lOlC C7 44A 102B 102C 40C-116A 102D'42B 40A 44B 102D Cg 46B 116B 116D 47D 116A 116D 48B 46A 46A 116C Cg 59A 116C 116D 57D 115B 116D 59D 53A 60C 116D Cato 95A 115B 114B 94C 115A 114B 95D 201B 97D 114D Cll 103A 188A 200C 200C 116B 200C 187D 83B 187C 200C C, 2 114A 115A 113C 113C 114D 113C 115B 116B 111B 113C C13 187B 122B 121C 180D 114B 121C 181D 199C 181C 119C Cl4 187A 120C 120D 60C 114C 120D 58C 201B 58D 119D C. s 79A 119B 119C 183C 114A-187B 185C 201C 181D 181D C16 200A 122A 187B 187C 187B 187C 200D 201A 183C 182A Table 7: Table for correspondence of colour codes based on Flower Council of Holland.
Codes Group 1-13 Yellow group 14-23 Yellow-Orange group 24-29 Orange group 30-35 Orange-Red group 36-56 Red group 57-74 Red-Purple group 75-79 Purple group 80-82 Purple-Violet group 83-88 Violet group 89 - 98 Violet - Blue group 99-110 Blue group 111-124 Blue-Green group 125-143 Green group 144-154 Yellow-Green group 155 White group 156-157 Grey-White group 158-159 Orange-White group 160-162 Greyed-Yellow group 163-177 Greyed-orange group 178-182 Greyed-Red group 183-187 Greyed-Purple group 188-198 Greyed-Green group 199-200 Brown group 201 Grey group 202Black group The various colours shown above are codified according to RHS colour chart in association with Flower Council of Holland and The Royal Horticultural Society, London
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The main advantages of the present invention are:
1. Herbal colourants offer an advantage in that they can be added or used without taking into consideration certification by different agencies like FAO, WHO and Cosmetic authorities etc.
2. The herbal colourants are safe, eco-friendly and health protective.
3. These herbal colourants may be used in more sensitive and delicate parts of the body like lips, cheeks and eyelids.
4. These herbal colourants can be used in leucoderma particularly of lips region.
S. The herbal colours are 100% lipophilic in nature.
6. The herbal colours are antimicrobial and anti-inflammatory.
7. The herbal colours are free from any strong side effects like carcinogenic effects to the users.
8. The herbal colours can be made in different shades in a cost-effective manner.
9. Addition of different essential oil and their isolates promotes the stimulation of creative
thoughts, enhance sensual feeling induce positive mental health and well being and to help ~~qnhance sen thorts to overcome the depressant feelings (anti-depressant).
Thus an aim of the present invention is to develop a safe and eco-friendly health protective and beauty enhancing herbal functional composition that contains only the natural products. The natural safe colour has been obtained and developed from different plant species belonging to the genus Arnebia, Bixa, Butea, Carthamus, Hibiscus, Jatropha, Lithospermum, Macrotomia, Maharanga, Nyctanthes, Onosma, Rhododendron and Tagetes. Various shades of colours were differentially extracted by following certain well-defined extraction methods. The invention also seeks to use
lipstick as a medium of aroma therapy. Essential oils isolated from different plants belonging to the genus Aquillaria, Cinnamomum, Cymbopogon, Elettaria, Eucalyptus, Geranium, Jasminum, Ocimum, Pelargonium, Rosa, Rosmarinus, Santalum and Vetiveria etc. Various blends of these essential oil isolates have been used to get desired effect like anti-depressant and creative thoughts.
Claims (81)
- CLAIMS : 1. A safe ecofdendly, health protective and beautifying herbal cosmetic composition containing herbal colourants together with a cosmetically acceptable amount of one or more additives providing special properties and a cosmetically acceptable base material.
- 2. A composition as claimed in claim 1 wherein, the additives providing special properties are selected from essential oils/aroma isolates obtained from the group of plant species belongingto genera Acquillaria, Cinnamomum, Cymbopogon Elettaria, Eucalyptus, Geranium, Jasminum, Ocimum, Pelargonium, Rosa, Rosmarinus, Santalum and Vetiveria.
- 3. A composition as claimed in claim 1 wherein, the essential oils/aroma isolates act as mood lifting agents, antidepressant agents, anti stress agents, sensual pleasure providing agents, creative thought inducing agents, anxiety reducing agent, refreshing agent, stimulant, soothing agents, anti oxidants, fixative, fragrants and antimicrobial.
- 4. A composition as claimed in claim 1 wherein, the essential oils/aroma isolates release neurochemicals in the brain through the receptors in mouth and nose and provide mood enhancement, sensual pleasure, anti-depressant and creative thought inducing properties.
- 5. A composition as claimed Jnclaml wherein, the colourants are isolated from specieces belong to the genera of the family Boraginaceae, which are non-toxic and free from any side effects.
- 6. A composition as claimed in claim 1 wherein, the colourant is obtained from the plantsbelonging to the genus Arnebia, Bixa, Butea, Carthamus, Hibiscus, Jatropha, Lithospermum, Macrotomia, Maharanga, Nyctanthes, Onosma, Rhododendron, and Tagetes
- 7. A composition as claimed in claim 1 wherein, the colourants are extracted from root, stem or leaves of the plants and the quantum of the essential oils used base on the part from which the essential oil is extracted.
- 8. A composition as claimed in claim 1 wherein, the colourants are soluble in organic solvents selected from hexane, petroleum ether, benzene, diethyl ether, ethylacetate, chloroform, acetone and alcohol in the range 30 to 100 %.
- 9. A composition as claimed in claim 1 wherein, the colourants has pH between 5 to 6.
- 10. A composition as claimed in claim 1 wherein the colourant is present in an amount of 0.1 to 10%.
- 11. A composition as claimed in claim 1 wherein the colourant are anti microbial, anti- inflammatery and are used in leucoderma more particularly of lips.<Desc/Clms Page number 27>
- 12. A composition as claimed in claim 1 wherein, the colourant has lipophilic properties.
- 13. A composition as claimed in claim 1 wherein, the colourant is a mixture of naphthazarins and/or cyclic unsaturated diketones in which double bonds and keto groups may be conjugated.
- 14. A composition as claimed in claim 1 wherein, the colourant has different shades of colours selected from purplish red, cerise, ruby red, beet root purple, dark violet, deep blue, blackish blue, pastel red, pale red, purplish red, rose red, cerise, ruby red, deep magenta, beet root purple, amaranth, dark purple, dark violet, deep violet, deep blue and blackish blue.
- 15. A composition as claimed in claim 1 wherein, the red colour of the colourant may be changed to different shades with organic and inorganic acids.
- 16. A composition as claimed in claim 15 wherein, the intensity of the red colour of the herbal colourant may be increased with organic acids and decreased with inorganic acids.
- 17. A composition as claimed in claim 15 wherein, the concentration of the acids is 1 to 20%.
- 18. A composition as claimedTiTclainri whereinTthe red'colour of the herbal colourant may be changed to different shades with organic and inorganic bases.
- 19. A composition as claimed in claim 18 wherein the intensity of the red colour of the herbal- - colourant may be increased with organic bases and decreased with inorganic bases.
- 20. A composition as claimed in claim 18 wherein the concentration of the bases is 1 to 20%.
- 21. A composition as claimed in claim 1 useful as a lipstick for man for aromatherapy.
- 22. A composition as claimed in claim 1 useful as an eye-shadow application.
- 23. A composition as claimed in claim 1 useful as a glow glitter.
- 24. A composition as claimed in claim 1 useful as a rose.
- 25. A composition as claimed in claim 1 wherein the essential used is in the range of traces to ppm.
- 26. A composition as claimed in claim 1 wherein the softening agents used are in the range of 0.5% to 2% of the total weight of the composition.
- 27. A composition as claimed in claim 1 wherein lusture producing agents are in the range of 0.5% to 2%.
- 28. A composition as claimed in claim 1 wherein skin protecting agents are in the range of 0.0001 to 0. 09%.
- 29. A composition as claimed in claim 1 wherein essential oil used for functional attributes range between 0.0001 to 0.009 %.<Desc/Clms Page number 28>
- 30. A composition as claimed in claim 1 wherein beeswax is used as a base material and forms the balance amount of the composition.
- 31. A composition as claimed in claim 1 wherein the aroma is provided by essential oils obtainedfrom the group of plant species belonging to genera Acquillaria, Cinnamomum, Cymbopogon Elettaria, Eucalyptus, Geranium, Jasminum, Ocimum, Pelargonium, Rosa, Rosmarinus, Santalum and Vetiveria.
- 32. A composition as claimed in claim 1 wherein the cosmaceutical application and use of extracted organic compound in lipsticks, eye shadow, glow glitters, rouges and skin conditioning agents.
- 33. A composition as claimed in claim 1 wherein the composition is a lipstick having improved moisturizing effect.
- 34. A composition as claimed in claim 1 wherein, the additives are a mixture of essential oils functioning as a mood-lifting agent, anti stress agent, anxiety reducing agent, sensual feeling agent, an anti-depressant agent, a creative thought inducing agent, a refreshing agent, anti oxidant, fixative and a stimulant.
- 35. A composition-as-jclaimedinclaim L wherein, anti-depressant property imparted by the essential oils are selected fromEssential Oils Preferred Ratio 1. Ocimum oil : Jasminum oil : Cymbopogon oil (1 : 2 : 1) 2. Ocimum oil : Mentha oil: Rosmarinus oil (2 : 1 : 1) 3. Jasminum oil : Mentha oil: Rosmarinus oil (1 : 1 : 1) 4. Cymbopogon oil : Ocimum oil : Mentha oil (1 : 2 : 1) 5. Ocimum oil: Cymbopogon oill (2 : 1) 6 Mentha oil : Rosmarinus oil (1 : 1) 7 Ocimum oil 8. Rosmarinus oil
- 36. A composition as claimed in claim 1 wherein, the creative thought-inducing property is imparted by the essential oils selected fromEssential oil Preferred rato 1 Tantalum oit 2 Santalum oil: Rosa oil (I : 2)<Desc/Clms Page number 29>
- 37. A composition as claimed in claim 1 wherein, the anti-stress property is imparted by the essential oils selected fromEssential oil Preferred ratio 1. Santalum oil: Lavandula oil (2: 1) 2. Lavandula oil : Eucalyptus oil : Rosa oil (1 : 1 : 1) 3. Eucalyptus oil: Rosa oil (1 : 2) 4. Aluillaria oil: Elettaria oil: Rosmarinus oil (1 : 1 : 1) 5. Jasminum oil (1 : 2) 6 Santalum oil 7 Lavandula oil
- 38. A composition as claimed in claiml wherein, the refreshing property is imparted by the essential oils selected fromEssential oil Preferred ratio 1. Santalum oil: Rosa oil: Rosmarinus oil (1 : 1 : 1) 2. Santalum oil: Pelargonium oil (1: 2) 2. Jasminum oil: Lavandula oil (1 : 2) 3. Santalum oil: Rosa oil (1 : 1) 4. Lavandula oil J. Santalum oil
- 39. A composition as claimed in claim 1 wherein, the sensual feeling property is imparted by the essential oils selected fromEssential oil Preferred ratio 1. Jasminum oil : Lavandula oil: Pelorgonium oil (1 : 2) 6 Ocimum oil: Jasminum oil: Cymbopogon oil (1: 2: 1) 7 Jasminum oil 8 Jasminum oil : Lavandula oil (2: 1)
- 40. A composition as claimed in claim 1 wherein, the mood lifting property is imparted by the essential oils selected fromEssential oil Preferred ratio 1. Jasminum oil : Rosa oil : Palergonium oil (I : 1: 1) 2. Rosmarinus oil 3. Cymbopogan oil : Rosa oil (2: 1) 4. Rosa oil 5. Jasmmum oil : Rosa oil
- 41. A composition as claimed in claim 1 wherein, the anxiety reducing property is imparted by the essential oils selected fromEssential oil Preferred ratio 1 Rosa Oil : Cinnamomum os 2)<Desc/Clms Page number 30>
- 42. A composition as claimed in claim 1 wherein, the anti-stress property is imparted by the aroma isolate Citral
- 43. A composition as claimed in claim 1 wherein, the refreshing property is imparted by the aroma isolate selected from linalol, benzyl alcohol, terpeneol, terpeneol and linaol at a preferred ratio of 1: 2.
- 44. A composition as claimed in claim 1 wherein, the sensual feeling property is imparted by the aroma isolate butyric acid.
- 45. A composition as claimed in claim 1 wherein, the creative thoughts property is imparted by the aroma isolate selected fromAroma Isolate Preferred ratio 1. Isobutyric acid: Butyric acid: linalo (1:2:1) 2. Isobutyruc acud: Benzyl alcohol: linalol (1:2:1) 3. Isobutyric acid: 4. Linalol: Isobutyric acid (1:2)
- 46. A composition as claimed in claim 1 wherein, the mood lifting property is imparted by the aroma isolate selected from jasmone, citral, eugenol, eugenol and citral at a preferred ratio 1: 2.
- 47. A composition as claimed in claim 1 wherein, the fixative is tocopherol and santulam oil, tocopherol also functions as fixative, which may present in traces to ppm.
- 48. A process for extraction of organic colourants from the plants, said process comprising obtaining the plant parts, extracting with organic solvents, removing the solvents by conventional methods, concentrating the extract under reduced pressure and optionally treating with acids or bases to produce various shades.
- 49. A process for the extraction of organic colourants, said process comprising the steps of : a) drying the plant parts, b) powdering the dried plant parts, c) subjecting the dry powder obtained in step (b) to Soxhlet extraction at a temperature in the range of 40-80 C or cold percolation with organic solvents at a temperature between 20 to 45 C, d) concentrating the mixture of step (c) by conventional methods at reduced pressure in the range of 50-100 psi and at a temperature not exceeding 50 C,<Desc/Clms Page number 31>e) mixing the concentrate of step (d) with silica gel in the ratio 1: 3 to 2: 7 to obtain a slurry, f) eluting the slurry with organic solvents resulting in various fractions, g) concentrating the fractions at a pressure in the range of 50-100 psi resulting in herbal colourants, optionally treating the said colours with acids or bases to produce various shades, and h) obtaining various colours from by treating the said fractions with acids or bases to produce colourants of various shades.
- 50. A process as claimed in claim 49 wherein, the organic solvent is selected from polar solvents, non-polar solvents or mixtures thereof.
- 51. A process as claimed in claim 49 wherein, the polar solvents are selected from acetone, chloroform, ethyl acetate, methanol and ethanol.
- 52. A process as claimed in claim 49 wherein, the non-polar solvents are selected from petroleum ether, hexane, toluene and cyclohexane
- 53. A process of extraction of herbal colourants from plants of the family Boraginaceae, which comprises ; percolating powdered plant parts with alcohol at room temperature resulting in alcohol soluble herbal material, the said herbal material being concentrated by known means at pressures in the range of 50-100 psi and at a temperature in the range of 40-60 C, the said concentrate being made into a slurry with silica gel in a ratio in the range of 1: 3 to 2: 7, the said slurry being eluted by known means with organic solvents resulting in fractions, the said fractions further being concentrated by known methods at a pressure in the range of 50-100 psi resulting in herbal colorants, optionally treating the said colours with acids or bases to produce various shades.
- 54. A process as claimed in claim 53 wherein, the plants are selected from the group of plants belonging to the family Boraginaceae
- 55. A process as claimed in claims 49 and 53 wherein, the plant parts are selected from root, stem and leaf the quantum of the essential oils used base on the part from which the essential oil is extracted
- 56. A process as claimed in claims 49 and 53 wherein, the plant parts are dried at a temperature in the range of 30-450 C, in shade.
- 57. A process as claimed in claims 49 and 53 wherein, the dried plant parts are powdered to particle size in the range of 30-60 mesh.<Desc/Clms Page number 32>
- 58. A process as claimed in claim 53 wherein, the alcohol used is selected from group consisting of methanol and ethanol.
- 59. A process as claimed in claim 53 wherein, the organic polar solvents are selected from acetone, chloroform, ethyl acetate, methanol and ethanol.
- 60. A process as claimed in claim 53 wherein, the non-polar solvents are selected from petroleum ether, hexane, toluene and cyclohexane
- 61. A process as claimed in claims 49 and 53 wherein, the ratio of polar and non-polar solvent caries according to the nature of the solvents.
- 62. A process as claimed in claims 49 and 53 wherein, the mixture of non-polar solvent to chloroform is prepared in the ratio of 99 : 1 to 0 : 100.
- 63. A process as claimed in claims 49 and 53 wherein, the colourants ranges from purplish red, cerise, ruby red, beetroot purple, dark violet, deep blue, blackish blue, pastel red, pale red, purplish red, rose red, cerise, ruby red, deep magenta, beet root purple, amaranth, dark purple, dark violet, deep violet, deep blue and bla-cldili blue.
- 64. A process as claimed in claims 49 and 53 wherein, the acid used is selected from the group consisting of organic acids such as formic acid and acetic acid, inorganic acids such as HC1, HN03 and H2SO4
- 65. A process as claimed in claims 49 and 53 wherein, the acid concentration is in the range of 0.1% to 10%.
- 66. A process as claimed in claims 49 and 53 wherein, the change of colour in the colourant is effected by treating the colourant with traces of food grade acids such as acetic acid, taken in an amount of 0. 1 %.
- 67. A process as claimed in claims 49 and 53 wherein, the change of colour in the colourant is effected by treating the colourant with traces of bases taken in an amount of 0. 1%.
- 68. A process as claimed in claims 49 and 53 wherein, the bases are selected from organic bases such as sodium acetate, potassium acetate and diethyl amine and inorganic bases such as NaOH, KOH, Na2C03 and NaCl
- 69. A process as claimed in claims 49 and 53 wherein, the concentration of the base is in the range of 0.1% to 20%.
- 70. A process as claimed in claims 49 and 53 wherein, the herbal colourant is antimicrobial, anti- inflammatory and is used in leucoderma more particularly of lips.<Desc/Clms Page number 33>
- 71. A composition according to any one of claims 1 to 47, formulated as a lipstick.
- 72. A composition according to any one of claims 1 to 47, formulated as eye- shadow.
- 73. A composition according to any one of claims 1 to 47, formulated as a skin cream.
- 74. A composition according to any one of claims 1 t o47, formulated as glow-glitter.
- 75. A composition according to any one of claims 1 to 47, formulated as rouge.
- 76. A safe eco friendly, health protective and beautifying herbal cosmetic composition, substantially as hereinbefore described.
- 77. A safe eco friendly, health protective and beautifying herbal cosmetic composition, substantially as hereinbefore described with reference to the accompanying drawings.
- 78. An organic colourant, extracted by means of a process according to any one of claims 48 to 52.
- 79. A herbal colourant from a plant of family Boraginaceae, extracted by means of a process according to any one of claims 53 to 70.
- 80. A process for extraction of organic colourants from plants, substantially as hereinbefore described.
- 81. A process for extraction of herbal colourants from plants of the family Boraginaceae, substantially as hereinbefore described.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001096849A JP2002308724A (en) | 2001-03-29 | 2001-03-29 | Safe, eco-friendly, health rpotective herbal color and aroma useful for cosmaceutical application |
FR0104411A FR2822678B1 (en) | 2001-03-29 | 2001-03-30 | VEGETABLE COLORING MATERIALS AND INOFFENSIVE, NON-POLLUTANT, PROTECTIVE PLANTS AND USES THEREOF FOR COSMETIC APPLICATIONS |
GB0108033A GB2374284B (en) | 2001-03-29 | 2001-03-30 | Safe eco-friendly health protective herbal colours and aroma useful for cosmaceutical applications |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001096849A JP2002308724A (en) | 2001-03-29 | 2001-03-29 | Safe, eco-friendly, health rpotective herbal color and aroma useful for cosmaceutical application |
FR0104411A FR2822678B1 (en) | 2001-03-29 | 2001-03-30 | VEGETABLE COLORING MATERIALS AND INOFFENSIVE, NON-POLLUTANT, PROTECTIVE PLANTS AND USES THEREOF FOR COSMETIC APPLICATIONS |
GB0108033A GB2374284B (en) | 2001-03-29 | 2001-03-30 | Safe eco-friendly health protective herbal colours and aroma useful for cosmaceutical applications |
Publications (3)
Publication Number | Publication Date |
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GB0108033D0 GB0108033D0 (en) | 2001-05-23 |
GB2374284A true GB2374284A (en) | 2002-10-16 |
GB2374284B GB2374284B (en) | 2004-09-29 |
Family
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GB0108033A Expired - Fee Related GB2374284B (en) | 2001-03-29 | 2001-03-30 | Safe eco-friendly health protective herbal colours and aroma useful for cosmaceutical applications |
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Country | Link |
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JP (1) | JP2002308724A (en) |
FR (1) | FR2822678B1 (en) |
GB (1) | GB2374284B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015144485A1 (en) * | 2014-03-28 | 2015-10-01 | Henkel Ag & Co. Kgaa | Olfactory boosters |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US7189419B2 (en) * | 2002-12-17 | 2007-03-13 | Avon Products, Inc. | Use of active extracts to lighten skin, lips, hair, and/or nails |
JP2007070291A (en) * | 2005-09-07 | 2007-03-22 | Naris Cosmetics Co Ltd | Sunscreen external lotion |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5460808A (en) * | 1991-05-15 | 1995-10-24 | Chanel, Inc. | Mascara composition |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5135440A (en) * | 1974-09-21 | 1976-03-25 | Shiseido Co Ltd | KARUSAMINTOFUMAKUOATSUKUSURUBENIZARA NO SEIHO |
FR2464711A1 (en) * | 1979-09-06 | 1981-03-20 | Pierre Arguel Christine | Beauty cream for make-up and treating the skin - contg. sea turtle and avocado oils, spermaceti emulsion and colourant |
FR2477872A1 (en) * | 1980-03-17 | 1981-09-18 | Fabre Sa Pierre | Natural colourant for use in hair colouring compsns. - prepd. by solvent extracting roots of Boraginaceae family of plants |
JPS5943448B2 (en) * | 1982-07-09 | 1984-10-22 | 一丸フアルコス株式会社 | Cosmetics containing pigmented powder of Sikon extract pigment |
FR2555447A1 (en) * | 1983-11-28 | 1985-05-31 | Audy Rowland Jeanne | Anti-sun cosmetic composition containing natural annatto: mixture of four natural vegetable oils. Annatto oil, product claimed as well as the methods of extraction |
JPS60215617A (en) * | 1984-04-12 | 1985-10-29 | Kao Corp | Weak-acidity bath preparation |
JPS6270315A (en) * | 1985-04-30 | 1987-03-31 | Mitsui Petrochem Ind Ltd | Powdery bathing agent |
JPH01268616A (en) * | 1988-04-20 | 1989-10-26 | Shiseido Co Ltd | Cosmetic |
JPH0757733B2 (en) * | 1990-10-09 | 1995-06-21 | 呉羽化学工業株式会社 | Awakening fragrance composition and cosmetics |
FR2689011B1 (en) * | 1992-03-25 | 1994-07-01 | Skrzypczak Edgard | COSMETIC PHYTOTHERAPIC PREPARATION FOR LIPS. |
DE4226173A1 (en) * | 1992-08-07 | 1994-02-10 | Solvay Fluor & Derivate | Bath additive |
JPH0826958A (en) * | 1994-07-14 | 1996-01-30 | Fuji Yakuhin Kogyo Kk | Sustainable fragrance and mask holding the same |
JPH08143418A (en) * | 1994-11-17 | 1996-06-04 | Daiwa Kasei Kk | Cosmetic |
JP4028604B2 (en) * | 1996-04-30 | 2007-12-26 | 株式会社林原生物化学研究所 | Red pigment, method for producing the same, and cosmetics using the same |
JPH09323918A (en) * | 1996-05-31 | 1997-12-16 | Shiseido Co Ltd | Sleep inducing cosmetic material |
JPH11343497A (en) * | 1998-05-29 | 1999-12-14 | Naris Cosmetics Co Ltd | Cosmetic |
JP2000212028A (en) * | 1999-01-27 | 2000-08-02 | Pola Chem Ind Inc | Preparation for external use for skin for treatment of stress disorder |
-
2001
- 2001-03-29 JP JP2001096849A patent/JP2002308724A/en active Pending
- 2001-03-30 GB GB0108033A patent/GB2374284B/en not_active Expired - Fee Related
- 2001-03-30 FR FR0104411A patent/FR2822678B1/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5460808A (en) * | 1991-05-15 | 1995-10-24 | Chanel, Inc. | Mascara composition |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015144485A1 (en) * | 2014-03-28 | 2015-10-01 | Henkel Ag & Co. Kgaa | Olfactory boosters |
Also Published As
Publication number | Publication date |
---|---|
GB2374284B (en) | 2004-09-29 |
GB0108033D0 (en) | 2001-05-23 |
FR2822678A1 (en) | 2002-10-04 |
FR2822678B1 (en) | 2005-04-29 |
JP2002308724A (en) | 2002-10-23 |
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