WO2008035691A1 - Moisturizing agent, cell-activating agent, skin-whitening agent, and antioxidant agent - Google Patents

Moisturizing agent, cell-activating agent, skin-whitening agent, and antioxidant agent Download PDF

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Publication number
WO2008035691A1
WO2008035691A1 PCT/JP2007/068126 JP2007068126W WO2008035691A1 WO 2008035691 A1 WO2008035691 A1 WO 2008035691A1 JP 2007068126 W JP2007068126 W JP 2007068126W WO 2008035691 A1 WO2008035691 A1 WO 2008035691A1
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Prior art keywords
agent
skin
extract
genus
plant
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PCT/JP2007/068126
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French (fr)
Japanese (ja)
Inventor
Akira Hatani
Yumiko Okumura
Hayami Maeda
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Noevir Co., Ltd.
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Publication of WO2008035691A1 publication Critical patent/WO2008035691A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/105Plant extracts, their artificial duplicates or their derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics 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
    • A61K8/9783Angiosperms [Magnoliophyta]
    • A61K8/9789Magnoliopsida [dicotyledons]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/16Emollients or protectives, e.g. against radiation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/18Antioxidants, e.g. antiradicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/08Anti-ageing preparations
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs

Definitions

  • the present invention relates to a moisturizer, cell activator, whitening agent, and antioxidant containing a plant extract as an active ingredient, and a skin external preparation and food containing the plant extract.
  • Patent Document 1 Japanese Patent Laid-Open No. 2001-131045
  • Patent Document 2 Japanese Patent Laid-Open No. 2003-89630
  • Patent Document 3 Japanese Patent Laid-Open No. 10-182413
  • Naturally-derived components are known to have various pharmacological and cosmetic effects, and so far many plants and fungi have been widely applied to fields such as external preparations for skin and foods and drinks.
  • Naturally-derived ingredients whose effects are not yet known, and the development of effective ingredients having excellent moisturizing action, cell activation action, whitening action or antioxidant action was expected.
  • the present invention has been made to find such an active ingredient, and is a humectant and a cell retentate that can be widely applied in the fields of external preparations for skin and foods and drinks. It aims at providing an active agent, a whitening agent, and an antioxidant.
  • the present inventors In order to find a moisturizer, a cell activator, a whitening agent, and an antioxidant that can be widely applied to fields such as external preparations for skin and foods and drinks, the present inventors have made various substances of natural origin. A study was conducted. As a result, the present inventors have found an excellent moisturizing action, cell activation action, whitening action and antioxidant action in extracts of plants belonging to the genus Tochinacea, and have further studied and completed the present invention. That is, the present invention provides a skin containing a moisturizer, a cell activator, a whitening agent, an antioxidant, and an extract of one or more plants of the plant belonging to the genus Tochina plant as an active ingredient. It provides external preparations and foods.
  • a moisturizer it is possible to provide a moisturizer, a cell activator, a whitening agent, and an antioxidant having excellent effects, and these can be blended in a composition such as a skin external preparation or food.
  • a composition such as a skin external preparation or food.
  • various compositions can be provided that exhibit excellent effects in preventing and improving various skin symptoms such as wrinkles, tarmi, skin firmness, spots, and kusumumi.
  • Androsace plants (Androsace chamaeiasme SPP.), Andros ace umbellata, Androsace filiformis, Kitakozakura, which are plants used as raw materials of the present invention (Androsac e septentrionalis) and Androsace erecia are well known.
  • the plant used as a raw material for the present invention is not particularly limited as long as it is a plant belonging to the genus Tochinaiso, but for reasons such as availability and effectiveness, Tochinaiso (Andro sace chamaeiasme spp.) It is particularly preferable to use Androsace erecia, which is preferred to use Anarosace umbellata, Androsace, etc.
  • the extract of the plant belonging to the genus Tochinaisu in the present invention includes the active ingredient and the dried product of the plant belonging to the genus Tochinaisu, but it is preferable to use the extract extracted using various solvents. Any part of the leaves, flowers, seeds, roots, stems, buds, etc., is used for extraction. However, it is better to use whole grass for easy use. In the extraction, it may be used as it is, but considering the extraction efficiency, it is preferable to carry out the extraction after processing such as shredding, drying, and pulverization. Extraction can also be performed by an extraction method using a force immersed in an extraction solvent, a supercritical fluid, or a subcritical fluid.
  • homogenization may be performed in stirring or an extraction solvent.
  • the extraction temperature is suitably from about 5 ° C to the boiling point of the extraction solvent.
  • the extraction time varies depending on the type of extraction solvent and the extraction temperature, but it is appropriate to set it to about 1 to 14 days.
  • Extraction solvents include water, lower alcohols such as methanol, ethanol, propanol, and isopropanol, polyhydric alcohols such as 1,3-butylene glycol, propylene glycol, dipropylene glycol, and glycerin, ethyl ether, and propyl ether. Solvents such as ethers such as butyl acetate and esters such as butyl acetate and ketones such as acetone and ethylmethylolene ketone, and one or more of these may be selected and used. Further, physiological saline, phosphate buffer, phosphate buffered saline, or the like may be used. Further, one or more supercritical fluids or subcritical fluids such as water, carbon dioxide, ethylene, propylene, ethanol, methanol, ammonia may be used.
  • lower alcohols such as methanol, ethanol, propanol, and isopropanol
  • polyhydric alcohols such as 1,3-
  • Extracts of the above-mentioned plants of the plant of the genus Tochina can be used as they are. Force concentrated and dried solids can be used again by dissolving them in water or a polar solvent, which impairs their physiological effects. It may be used after performing purification treatment such as decolorization, deodorization, desalting, etc., and fractionation treatment by column chromatography etc. within the range.
  • the aforementioned extract of Tochina is also lyophilized after each treatment and fractionation and dissolved before use.
  • An extract of a plant belonging to the genus Tochinais has excellent moisturizing action, cell activation action, whitening action and antioxidant action, and should be used as a moisturizing agent, cell activator, whitening agent and antioxidant. Can do.
  • moisturizers, cell activators, whitening agents, and antioxidants that contain extracts of the plants of the genus Tochina is useful for hair and can be taken orally, not just for topical use. It can also be applied to beverages or pharmaceuticals.
  • a moisturizing agent containing an extract of the plant of the genus Tochina is effective against skin and hair.
  • the moisturizing effect is exerted, and the moisturizing effect on the skin is particularly high.
  • a cell activator comprising an extract of a plant belonging to the genus Tochina is effective for various cells, but particularly effective for dermal fibroblasts.
  • a whitening agent containing an extract of the plant of the genus Tochina is effective for improving pigmentation symptoms such as stains and freckles, and is particularly effective for suppressing melanin production.
  • An antioxidant comprising an extract of a plant belonging to the genus Tochina is effective as an active ingredient, but particularly exhibits an excellent free radical scavenging effect.
  • an extract of the plant of the genus Tochina is used in an external preparation for skin, it has an excellent effect in preventing and improving skin symptoms such as wrinkles, tarmi, skin firmness, spots, Tasumi, dryness, and fine wrinkles. It can be used as a skin external preparation for moisturizing, a skin external preparation for whitening, or a skin external preparation for improving anti-aging.
  • the extract of the plant of the genus Tochina can also be used for foods (including general foods and functional foods).
  • the food of the present invention includes beverages.
  • Functional food as used herein refers to foods taken for the purpose of maintaining health or providing nutrition instead of diet, such as health foods, nutritional supplements, supplements, and nutritional foods.
  • the amount of the extract of the plant belonging to the genus Tochina is mixed with the external preparation for skin can be adjusted depending on the type of external preparation for skin use and the purpose of use, etc. 0001-50. 0 weight 0/0 mosquitoes preferably 0. for ⁇ , is more preferably ⁇ (or, 0. 001-25. 0 by weight%.
  • the dosage form of the external preparation for skin containing the extract of the plant of the genus Tochina is arbitrary, and for example, it is provided as a solubilizing system such as lotion, an emulsifying system such as cream or emulsion, or a dispersing system such as calamine lotion. I can do it. Furthermore, it can also be provided in various dosage forms such as aerosols, ointments, powders and granules filled with a propellant.
  • the topical skin preparation containing the extract of the plant of the genus Tochina is, in addition to the extract of the plant of the genus Tochina, as required, usually a pharmaceutical product, quasi-drug, skin cosmetic, hair Oily ingredients, moisturizers, powders, pigments, emulsifiers, solubilized in cosmetics and detergents Agents, cleaning agents, ultraviolet absorbers, thickeners, drugs, fragrances, resins, antibacterial / antifungal agents, alcohols, and the like can be appropriately blended.
  • other moisturizers, cell activators, whitening agents, or antioxidants can be used in combination as long as the effects of the present invention are not impaired.
  • the plant was introduced into a supercritical extractor and extracted with a supercritical fluid of carbon dioxide at 40 ° C under a pressure of 15 MPa.
  • the extract was collected to obtain an extract of the genus Tochinaiso.
  • the evaluation was performed according to the following procedure. Normal human dermal fibroblasts were seeded in a 96-well microplate at 2.0 ⁇ 10 4 cells per well.
  • the seeding medium contains Dulbecco's modified One dull medium (DMEM) supplemented with 1% fetal bovine serum was used. After culturing for 24 hours, the medium was replaced with a test medium to which a sample of an arbitrary concentration was added, and further cultured for 48 hours. Next, replace the medium with 400 g / mL of 3- (4,5 dimethyl-2 thiazolyl) -2,5 diphenyltetrazolium bromide (MTT) and incubate for 2 hours to open the tetrazolium ring.
  • DMEM Dulbecco's modified One dull medium
  • MTT diphenyltetrazolium bromide
  • the formazan produced by the extraction was extracted with 2-propanol, and the absorbance at 550 nm was measured with a microplate reader. At the same time, the absorbance at 650 nm was measured as turbidity, and the cell activation action was evaluated by the difference between the two measured values.
  • the evaluation results are shown in Table 1 as relative values with the cell activation effect in the blank with no sample taken as 100. In the table, ** indicates a significance probability of less than 1% (P ⁇ 0.01) with respect to significance P value in t test.
  • the evaluation was performed according to the following procedure. Normal human epidermis cells were seeded in 96-well microplates at 2.0 ⁇ 10 4 cells per well. Commercially available Hume dia-KG2 manufactured by Kurabo Industries was used as the seeding medium. After culturing for 24 hours, the medium was replaced with the test medium to which the sample was added, and further cultured for 24 hours. Subsequently, the medium containing 100 g / mL of 3- (4,5 dimethyl 2 thiazolyl) 2,5 diphenyltetrazolium bromide (MTT) was exchanged and cultured for 2 hours. And the absorbance at 550 nm was measured with a microplate reader.
  • the evaluation was performed according to the following procedure. Normal human epidermal melanocytes manufactured by Kurabo Industries Co., Ltd. were seeded in a 96-well microplate so that there were 3.0 ⁇ 10 4 cells per well. As a seeding medium, Mediuml 54S manufactured by Kurabo Industries was used. After 24 hours, the medium was replaced with a medium containing each concentration of sample, and the cells were further cultured for 48 hours. Next, the solution was replaced with 75 L of 1 wt% 13 ⁇ 4101-X-containing phosphate buffer to completely dissolve the cells, and 50 L was used as a crude enzyme solution. The crude enzyme solution was added with 50 li UDO.
  • Table 3 shows the tyrosinase activity inhibition rate of the sample as a relative value to the tyrosinase activity inhibition rate in the blank with no sample added.
  • the evaluation was performed according to the following procedure. 100 L of a solution of an extract of a Tochina genus plant diluted to an arbitrary concentration with a 50% by weight aqueous ethanol solution was added to a 96-well microplate. . Next, 100 L of 1,1-diphenyl-2-picrylhydrazinole (DPPH) solution prepared in ethanol to a concentration of 0.2 mM was added to a 96-well microplate. The mixture was left standing in a place with stirring, and the absorbance at 516 nm was measured after 24 hours. When the absorbance of the blank to which the sample was not added was (A) and the absorbance when the sample was added was (B), the value of equation (1) was the radial elimination rate. The evaluation results are shown in Table 4.
  • the oil phase components (1) to 1 ⁇ 2) are heated and dissolved at 80 ° C.
  • the aqueous phase components (7) to (10) are heated and dissolved at 80 ° C.
  • the oil phase component is added to this while stirring and uniformly emulsified with a homogenizer. After emulsification, start cooling and add (11) and (12) sequentially and mix evenly.
  • Production method Dissolve ( 2 ) and (3) in (1). After dissolution, sequentially add ( 4 ) to (8), then stir well, add (9), and mix uniformly.
  • the oil phase components (1) to 1 ⁇ 2) are heated and dissolved at 80 ° C.
  • the aqueous phase components (7) to (10) are heated and dissolved at 80 ° C.
  • the oil phase component is added to this while stirring and uniformly emulsified with a homogenizer. After emulsification, add (11), start cooling, add (12) at 40 ° C and mix uniformly.
  • the aqueous phase components (1) to 1 ⁇ 2) are mixed and dissolved by heating at 75 ° C.
  • the oil phase components (7) to (14) are mixed and dissolved by heating at 75 ° C.
  • the oil phase component is added to the aqueous phase component and preliminary emulsification is performed, followed by uniform emulsification with a homomixer. Start cooling after emulsification and add (15) at 50 ° C. Cool to 40 ° C and add (16) to mix evenly. Match.
  • Production method Add (1) to (2), stir uniformly, and then add (3). After stirring uniformly, add (5) previously dissolved in (4). After stirring uniformly, add (6) to (8) previously mixed and stir and mix uniformly.
  • Production method Dissolve (1) and (2) uniformly. Add (3) and (4) to this, and mix evenly.
  • Tochinaiso plant extract [Production Example 3] 1.0 Production method: The oil phase components (1) to (4) are heated and dissolved at 80 ° C. On the other hand, the water phase components (5) to (7) are heated and dissolved at 80 ° C, and the oil phase components are mixed and stirred uniformly. Start cooling, add (8) at 40 ° C, and mix uniformly.
  • the oil phase components (1) to (4) are mixed and dissolved by heating at 75 ° C.
  • the aqueous phase components (5) to (7) are mixed, dissolved by heating at 75 ° C, and the pigments (8) to (10) are added thereto and dispersed uniformly with a homomixer.
  • the oil phase component is added to the water phase component and emulsified with a homomixer. Start cooling after emulsification, add ingredients (11) and (12) at 40 ° C and mix evenly.
  • the oil phase components (1) to 1 ⁇ 2) are mixed and dissolved by heating at 75 ° C.
  • the water phase components (7) to (10) are mixed, dissolved by heating at 75 ° C, and the pigments (11) to (15) are added to this and dispersed uniformly with a homomixer.
  • Manufacturing method Dissolve (5) and (6) in a part of (11) to 50 ° C, and gradually add to (4) heated to 50 ° C while stirring. After mixing this, disperse uniformly into (1) to (3), which is heated and dissolved at 70 ° C. Add (7) to (10), which is dissolved in the remainder of (11) by heating at 70 ° C while stirring, and emulsify with a homomixer. Start cooling after emulsification, add (12) at 40 ° C, and mix evenly.
  • Manufacturing method (2) and (3) are mixed, heated to 80 ° C, and then dissolved in (1) heated to 80 ° C. After evenly dissolving, add (4) and (5) and start cooling with stirring. Cool to 40 ° C, add (6) and (7), and mix evenly.
  • Production method (1) to (4) are mixed uniformly.
  • the oil phase components (1) to 1 ⁇ 2) are mixed and heated and dissolved at 75 ° C.
  • the aqueous phase components (7) to (10) are dissolved by heating at 75 ° C, and the oil phase component is added and emulsified with a homomixer. Start cooling after emulsification, add ingredients (11) and (12) at 40 ° C and mix evenly
  • Production method Components (1) to (4) are mixed and homogenized.
  • Production method (1) to (3) were respectively sieved and mixed, and then (4) to (5) were added and mixed. Thereafter, tableting was performed by a conventional method to obtain a tablet having a total amount of 600 mg.
  • the humectant, cell activator, whitening agent, and antioxidant of the present invention are useful for blending into skin external preparations, foods, pharmaceuticals, and quasi drugs.
  • the extract of the plant of the genus Tochinacea according to the present invention may be a component derived from nature and has great significance as a skin external preparation and a food ingredient. Useful as food.

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Abstract

An active ingredient having excellent moisturizing, cell-activating, skin-whitening or anti-oxidant effect is now found. Provided is a moisturizing agent, a cell-activating agent, a skin-whitening agent or an antioxidant agent which can be widely applied to the fields of external preparations to the skin and foods. An extract of a plant belonging to the genus Androsace, which has an excellent moisturizing, cell-activating, skin-whitening or anti-oxidant effect, is used as an active ingredient of a moisturizing agent, a cell-activating agent, a skin-whitening agent or an anti-oxidant agent. The extract of a plant belonging to the genus Androsace can be added to a composition such as an external preparation for the skin and a food. Thus, it becomes possible to provide various compositions having an excellent moisturizing, cell-activating, skin-whitening or anti-oxidant effect.

Description

明 細 書  Specification
保湿剤、細胞賦活剤、美白剤、及び抗酸化剤  Moisturizer, cell activator, whitening agent, and antioxidant
技術分野  Technical field
[0001] 本発明は、植物の抽出物を有効成分とする保湿剤、細胞賦活剤、美白剤、及び抗 酸化剤、ならびに植物の抽出物を含有する皮膚外用剤及び食品に関する。  [0001] The present invention relates to a moisturizer, cell activator, whitening agent, and antioxidant containing a plant extract as an active ingredient, and a skin external preparation and food containing the plant extract.
背景技術  Background art
[0002] 加齢、紫外線、ストレスなどによるシヮ、シミ、皮膚の弾性低下といった皮膚症状の 要因として、乾燥、細胞機能低下、紫外線によるメラニン産生や色素沈着、真皮マトリ ックス成分の減少や変性、紫外線等による細胞の酸化傷害などが挙げられる。このよ うな皮膚症状を防止 ·改善するために、様々な有効成分の検索及び配合検討が従来 なされてきた。細胞賦活剤としては、ボンカンのエッセンス(特許文献 1参照)、美白 剤としては、白鶴霊芝の水および/または有機溶媒抽出物(特許文献 2参照)、抗酸 化剤としては、サルォガセ科サルォガセ属植物の抽出物(特許文献 3参照)が知られ ている。  [0002] Causes of skin symptoms such as aging, UV rays, stress-induced skin wrinkles, spots, and skin elasticity reduction include dryness, decreased cellular function, melanin production and pigmentation due to UV rays, reduction and degeneration of dermal matrix components, Examples include oxidative damage of cells due to ultraviolet rays and the like. In order to prevent and improve such skin symptoms, various active ingredients have been searched and formulated. As the cell activator, the essence of Bonkan (see Patent Document 1), as the whitening agent, the water and / or organic solvent extract of Hakutsuru Reishi (see Patent Document 2), and as the antioxidant, the Salogase family Salogase An extract of a genus plant (see Patent Document 3) is known.
[0003] なお、トチナイソゥ属植物の抽出物を有効成分とする保湿剤、細胞賦活剤、美白剤 、及び抗酸化剤に関する先行技術は認められなかった。  [0003] It should be noted that no prior art relating to a moisturizer, a cell activator, a whitening agent, and an antioxidant containing an extract of a plant of the genus Tochina is recognized.
特許文献 1:特開 2001— 131045号公報  Patent Document 1: Japanese Patent Laid-Open No. 2001-131045
特許文献 2:特開 2003— 89630号公報  Patent Document 2: Japanese Patent Laid-Open No. 2003-89630
特許文献 3:特開平 10— 182413号公報  Patent Document 3: Japanese Patent Laid-Open No. 10-182413
発明の開示  Disclosure of the invention
発明が解決しょうとする課題  Problems to be solved by the invention
[0004] 天然由来成分は、様々な薬理作用や美容効果を有することが知られ、これまでにも 多数の植物や菌類などが皮膚外用剤や飲食品などの分野に幅広く応用されている 。しかし、天然由来成分の中には未だその効果が知られていないものも数多く存在し 、優れた保湿作用、細胞賦活作用、美白作用あるいは抗酸化作用を有する有効成 分の開発が期待されていた。本発明は、このような有効成分を見出すためになされた ものであり、皮膚外用剤や飲食品などの分野に幅広く応用が可能な保湿剤、細胞賦 活剤、美白剤、及び抗酸化剤を提供することを目的とする。 [0004] Naturally-derived components are known to have various pharmacological and cosmetic effects, and so far many plants and fungi have been widely applied to fields such as external preparations for skin and foods and drinks. However, there are many naturally-derived ingredients whose effects are not yet known, and the development of effective ingredients having excellent moisturizing action, cell activation action, whitening action or antioxidant action was expected. . The present invention has been made to find such an active ingredient, and is a humectant and a cell retentate that can be widely applied in the fields of external preparations for skin and foods and drinks. It aims at providing an active agent, a whitening agent, and an antioxidant.
課題を解決するための手段  Means for solving the problem
[0005] 本発明者らは、皮膚外用剤や飲食品などの分野に幅広く応用が可能な保湿剤、細 胞賦活剤、美白剤、及び抗酸化剤を見出すために、天然由来の種々の物質につい て検討を行った。その結果、トチナイソゥ属植物の抽出物に優れた保湿作用、細胞 賦活作用、美白作用、及び抗酸化作用を見出し、さらに検討を重ね、本発明を完成 するに至った。すなわち、本発明は、トチナイソゥ属植物を有効成分とする保湿剤、 細胞賦活剤、美白剤、及び抗酸化剤、並びにトチナイソゥ属植物の 1種または 2種以 上の植物の抽出物を含有する皮膚外用剤及び食品を提供するものである。 [0005] In order to find a moisturizer, a cell activator, a whitening agent, and an antioxidant that can be widely applied to fields such as external preparations for skin and foods and drinks, the present inventors have made various substances of natural origin. A study was conducted. As a result, the present inventors have found an excellent moisturizing action, cell activation action, whitening action and antioxidant action in extracts of plants belonging to the genus Tochinacea, and have further studied and completed the present invention. That is, the present invention provides a skin containing a moisturizer, a cell activator, a whitening agent, an antioxidant, and an extract of one or more plants of the plant belonging to the genus Tochina plant as an active ingredient. It provides external preparations and foods.
発明の効果  The invention's effect
[0006] 本発明によれば、優れた効果を有する保湿剤、細胞賦活剤、美白剤、及び抗酸化 剤を提供することができ、これらを皮膚外用剤や食品等の組成物に配合することによ り、シヮ、タルミ、肌のハリ、シミ、クスミといった種々の皮膚症状の防止や改善に優れ た効果を発揮する様々な組成物を提供することができる。  [0006] According to the present invention, it is possible to provide a moisturizer, a cell activator, a whitening agent, and an antioxidant having excellent effects, and these can be blended in a composition such as a skin external preparation or food. As a result, various compositions can be provided that exhibit excellent effects in preventing and improving various skin symptoms such as wrinkles, tarmi, skin firmness, spots, and kusumumi.
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[0007] 本発明の原料 して用いられる植物であるトチナイソゥ属(Androsace)植物 して (ま、トテナイソゥ(Androsace chamaeiasme SPP.) ,リュヮキユウコザクラ (Andros ace umbellata) ,サカコサクラ(Androsace filiformis)、キタコザクラ (Androsac e septentrionalis)■、アンドロサセ ·エレシァ(Androsace erecia)など力知られて いる。  [0007] Androsace plants (Androsace chamaeiasme SPP.), Andros ace umbellata, Androsace filiformis, Kitakozakura, which are plants used as raw materials of the present invention (Androsac e septentrionalis) and Androsace erecia are well known.
[0008] 本発明に用いられる原料となる植物は、トチナイソゥ属植物であれば特に限定され ないが、入手が比較的容易であることや有効性などの理由から、トチナイソゥ(Andro sace chamaeiasme spp.) ,リュ'ノキユウコ j クフ (Anarosace umbellata 、 ノ'ン ドロサセ.エレシァ(Androsace などを用いることが好ましぐアンドロサセ' エレシァ (Androsace erecia)を用いることが有効性の点から特に好ましレ、。  [0008] The plant used as a raw material for the present invention is not particularly limited as long as it is a plant belonging to the genus Tochinaiso, but for reasons such as availability and effectiveness, Tochinaiso (Andro sace chamaeiasme spp.) It is particularly preferable to use Androsace erecia, which is preferred to use Anarosace umbellata, Androsace, etc.
[0009] 本発明におけるトチナイソゥ属植物の抽出物には、トチナイソゥ属植物の原体や乾 燥物も含まれるが、各種溶媒を用いて抽出した抽出物を用いるのが好ましい。抽出 には、トチナイソゥ属植物の葉、花、種子、根、茎、芽などのいずれの部位を用いても 構わないが、簡便に利用するには全草を用いるとよい。抽出の際は、生のまま用いて もよいが、抽出効率を考えると、細切、乾燥、粉砕等の処理を行った後に抽出を行う ことが好ましい。抽出は、抽出溶媒に浸漬する力、、超臨界流体や亜臨界流体を用い た抽出方法でも行うことができる。抽出効率を上げるため、撹拌や抽出溶媒中でホモ ジナイズしてもよい。抽出温度としては、 5°C程度から抽出溶媒の沸点以下の温度と するのが適切である。抽出時間は抽出溶媒の種類や抽出温度によっても異なるが、 1時間〜 14日間程度とするのが適切である。 [0009] The extract of the plant belonging to the genus Tochinaisu in the present invention includes the active ingredient and the dried product of the plant belonging to the genus Tochinaisu, but it is preferable to use the extract extracted using various solvents. Any part of the leaves, flowers, seeds, roots, stems, buds, etc., is used for extraction. However, it is better to use whole grass for easy use. In the extraction, it may be used as it is, but considering the extraction efficiency, it is preferable to carry out the extraction after processing such as shredding, drying, and pulverization. Extraction can also be performed by an extraction method using a force immersed in an extraction solvent, a supercritical fluid, or a subcritical fluid. In order to increase the extraction efficiency, homogenization may be performed in stirring or an extraction solvent. The extraction temperature is suitably from about 5 ° C to the boiling point of the extraction solvent. The extraction time varies depending on the type of extraction solvent and the extraction temperature, but it is appropriate to set it to about 1 to 14 days.
[0010] 抽出溶媒としては、水の他、メタノール、エタノール、プロパノール、イソプロパノー ル等の低級アルコール、 1、 3—ブチレングリコール、プロピレングリコール、ジプロピ レングリコール、グリセリン等の多価アルコール、ェチルエーテル、プロピルエーテル 等のエーテル類、酢酸ブチル、酢酸ェチル等のエステル類、アセトン、ェチルメチノレ ケトン等のケトン類などの溶媒を用いることができ、これらより 1種又は 2種以上を選択 して用いる。また、生理食塩水、リン酸緩衝液、リン酸緩衝生理食塩水等を用いても よい。さらに、水や二酸化炭素、エチレン、プロピレン、エタノール、メタノーノレ、アンモ ユアなどの 1種又は 2種以上の超臨界流体や亜臨界流体を用いてもよい。  [0010] Extraction solvents include water, lower alcohols such as methanol, ethanol, propanol, and isopropanol, polyhydric alcohols such as 1,3-butylene glycol, propylene glycol, dipropylene glycol, and glycerin, ethyl ether, and propyl ether. Solvents such as ethers such as butyl acetate and esters such as butyl acetate and ketones such as acetone and ethylmethylolene ketone, and one or more of these may be selected and used. Further, physiological saline, phosphate buffer, phosphate buffered saline, or the like may be used. Further, one or more supercritical fluids or subcritical fluids such as water, carbon dioxide, ethylene, propylene, ethanol, methanol, ammonia may be used.
[0011] トチナイソゥ属植物の上記溶媒による抽出物は、そのままでも使用することができる 力 濃縮、乾固した物を水や極性溶媒に再度溶解して使用することもでき、これらの 生理作用を損なわない範囲で脱色、脱臭、脱塩等の精製処理やカラムクロマトグラフ ィ一等による分画処理を行った後に用いてもよい。トチナイソゥ属植物の前記抽出物 やその処理物及び分画物は、各処理及び分画後に凍結乾燥し、用時に溶解して用 いることあでさる。  [0011] Extracts of the above-mentioned plants of the plant of the genus Tochina can be used as they are. Force concentrated and dried solids can be used again by dissolving them in water or a polar solvent, which impairs their physiological effects. It may be used after performing purification treatment such as decolorization, deodorization, desalting, etc., and fractionation treatment by column chromatography etc. within the range. The aforementioned extract of Tochina is also lyophilized after each treatment and fractionation and dissolved before use.
[0012] トチナイソゥ属植物の抽出物は、優れた保湿作用、細胞賦活作用、美白作用、及 び抗酸化作用を有し、保湿剤、細胞賦活剤、美白剤、及び抗酸化剤として利用する ことができる。また、トチナイソゥ属植物の抽出物を有効成分とする保湿剤、細胞賦活 剤、美白剤、及び抗酸化剤は、皮膚に外用するだけではなぐ毛髪に利用することや 経口摂取も可能であり、食品、飲料、あるいは医薬品などにも応用することが可能で ある。  [0012] An extract of a plant belonging to the genus Tochinais has excellent moisturizing action, cell activation action, whitening action and antioxidant action, and should be used as a moisturizing agent, cell activator, whitening agent and antioxidant. Can do. In addition, moisturizers, cell activators, whitening agents, and antioxidants that contain extracts of the plants of the genus Tochina is useful for hair and can be taken orally, not just for topical use. It can also be applied to beverages or pharmaceuticals.
[0013] トチナイソゥ属植物の抽出物を有効成分とする保湿剤は、皮膚や毛髪に対して優 れた保湿作用を発揮し、特に皮膚に対する保湿効果が高い。 [0013] A moisturizing agent containing an extract of the plant of the genus Tochina is effective against skin and hair. The moisturizing effect is exerted, and the moisturizing effect on the skin is particularly high.
[0014] トチナイソゥ属植物の抽出物を有効成分とする細胞賦活剤は、種々の細胞に対し て優れた賦活作用を発揮するが、特に真皮線維芽細胞に対して優れた効果を発揮 する。 [0014] A cell activator comprising an extract of a plant belonging to the genus Tochina is effective for various cells, but particularly effective for dermal fibroblasts.
[0015] トチナイソゥ属植物の抽出物を有効成分とする美白剤は、シミ 'ソバカスといった色 素沈着症状の改善に効果を発揮し、特にメラニンの産生抑制に対して優れた効果を 発揮する。  [0015] A whitening agent containing an extract of the plant of the genus Tochina is effective for improving pigmentation symptoms such as stains and freckles, and is particularly effective for suppressing melanin production.
[0016] トチナイソゥ属植物の抽出物を有効成分とする抗酸化剤は、優れた抗酸化作用を 発揮するが、特にフリーラジカル消去作用に優れた効果を発揮する。  [0016] An antioxidant comprising an extract of a plant belonging to the genus Tochina is effective as an active ingredient, but particularly exhibits an excellent free radical scavenging effect.
[0017] また、トチナイソゥ属植物の抽出物を皮膚外用剤に配合することにより、シヮ、タルミ 、肌のハリ、シミ、タスミ、乾燥、小じわ等の皮膚症状の防止 ·改善に優れた効果を発 揮する皮膚外用剤を得ることができ、保湿用皮膚外用剤、美白用皮膚外用剤、ある いは老化防止改善用皮膚外用剤として用いることができる。さらに、トチナイソゥ属植 物の抽出物は、食品(一般の食品、機能性食品を含む)にも用いることもできる。なお 、本発明の食品には飲料も含まれる。ここで言う機能性食品とは、健康食品、栄養補 助食品、サプリメント、栄養食品等、健康の維持あるいは食事に代わり栄養補給の目 的で摂取する食品を意味してレ、る。  [0017] In addition, by incorporating an extract of the plant of the genus Tochina is used in an external preparation for skin, it has an excellent effect in preventing and improving skin symptoms such as wrinkles, tarmi, skin firmness, spots, Tasumi, dryness, and fine wrinkles. It can be used as a skin external preparation for moisturizing, a skin external preparation for whitening, or a skin external preparation for improving anti-aging. Furthermore, the extract of the plant of the genus Tochina can also be used for foods (including general foods and functional foods). The food of the present invention includes beverages. Functional food as used herein refers to foods taken for the purpose of maintaining health or providing nutrition instead of diet, such as health foods, nutritional supplements, supplements, and nutritional foods.
[0018] トチナイソゥ属植物の抽出物を皮膚外用剤に配合する際の配合量は、皮膚外用剤 の種類や使用目的等によって調整することができるが、効果や安定性などの点から、 全量に対して 0. 0001-50. 0重量0 /0カ好まし <、より好まし < (ま、 0. 001-25. 0重 量%である。 [0018] The amount of the extract of the plant belonging to the genus Tochina is mixed with the external preparation for skin can be adjusted depending on the type of external preparation for skin use and the purpose of use, etc. 0001-50. 0 weight 0/0 mosquitoes preferably 0. for <, is more preferably <(or, 0. 001-25. 0 by weight%.
[0019] トチナイソゥ属植物の抽出物を配合する皮膚外用剤の剤型は任意であり、例えば、 ローションなどの可溶化系、クリームや乳液などの乳化系、カラミンローション等の分 散系として提供すること力できる。さらに、噴射剤と共に充填したエアゾール、軟膏剤 、粉末、顆粒などの種々の剤型で提供することもできる。  [0019] The dosage form of the external preparation for skin containing the extract of the plant of the genus Tochina is arbitrary, and for example, it is provided as a solubilizing system such as lotion, an emulsifying system such as cream or emulsion, or a dispersing system such as calamine lotion. I can do it. Furthermore, it can also be provided in various dosage forms such as aerosols, ointments, powders and granules filled with a propellant.
[0020] なお、トチナイソゥ属植物の抽出物を配合する皮膚外用剤には、トチナイソゥ属植 物の抽出物の他に、必要に応じて、通常医薬品、医薬部外品、皮膚化粧料、毛髪用 化粧料及び洗浄料に配合される、油性成分、保湿剤、粉体、色素、乳化剤、可溶化 剤、洗浄剤、紫外線吸収剤、増粘剤、薬剤、香料、樹脂、防菌防黴剤、アルコール類 等を適宜配合することができる。また、本発明の効果を損なわない範囲において、他 の保湿剤、細胞賦活剤、美白剤、あるいは抗酸化剤との併用も可能である。 [0020] It should be noted that the topical skin preparation containing the extract of the plant of the genus Tochina is, in addition to the extract of the plant of the genus Tochina, as required, usually a pharmaceutical product, quasi-drug, skin cosmetic, hair Oily ingredients, moisturizers, powders, pigments, emulsifiers, solubilized in cosmetics and detergents Agents, cleaning agents, ultraviolet absorbers, thickeners, drugs, fragrances, resins, antibacterial / antifungal agents, alcohols, and the like can be appropriately blended. In addition, other moisturizers, cell activators, whitening agents, or antioxidants can be used in combination as long as the effects of the present invention are not impaired.
実施例  Example
[0021] 以下にトチナイソゥ属植物の抽出物の製造例、各作用を評価するための試験、皮 膚外用剤や食品としての処方例、使用試験についてさらに詳細に説明するが、本発 明の技術的範囲はこれによってなんら限定されるものではない。  [0021] In the following, production examples of extracts of the genus Tochina plant, tests for evaluating each action, formulation examples for skin external preparations and foods, and use tests will be described in more detail. The target range is not limited at all by this.
[0022] [製造例 1] [0022] [Production Example 1]
トチナイソゥ属植物の乾燥粉砕物 lkgに 50重量%エタノール水溶液を 10リットル加 え、室温で 7日間浸漬した。抽出液をろ過して回収し、溶媒を除去した後、トチナイソ ゥ属植物の抽出物を得た。  10 liters of 50% by weight ethanol aqueous solution was added to 1 kg of dried pulverized product of Tochina, and soaked at room temperature for 7 days. The extract was collected by filtration, and after removing the solvent, an extract of the plant of the genus Tochina was obtained.
[0023] [製造例 2] [0023] [Production Example 2]
トチナイソゥ属植物の乾燥粉砕物 lkgに水を 9リットル加え、 90°Cにて 6時間還流し て抽出した。抽出液をろ過して回収し、溶媒を除去した後、トチナイソゥ属植物の抽 出物を得た。  9 liters of water was added to 1 kg of dry ground pulverized product of Tochina, and the mixture was extracted by refluxing at 90 ° C for 6 hours. The extract was collected by filtration, and after removing the solvent, an extract of the plant of the genus Tochina is obtained.
[0024] [製造例 3] [0024] [Production Example 3]
トチナイソゥ属植物の乾燥粉砕物 lkgにメタノールを 9リットル加え、室温で 7日間浸 漬した。抽出液をろ過して回収し、溶媒を除去した後、トチナイソゥ属植物の抽出物 を得た。  Nine liters of methanol was added to 1 kg of dry ground pulverized Tochina, and soaked at room temperature for 7 days. The extract was collected by filtration, and after removing the solvent, an extract of the genus Tochinaiso was obtained.
[0025] [製造例 4] [0025] [Production Example 4]
超臨界抽出装置にトチナイソゥ属植物を投入し、 40°Cにおいて 15MPaの気圧下 で二酸化炭素の超臨界流体を用いて抽出した。抽出物を回収し、トチナイソゥ属植 物の抽出物を得た。  The plant was introduced into a supercritical extractor and extracted with a supercritical fluid of carbon dioxide at 40 ° C under a pressure of 15 MPa. The extract was collected to obtain an extract of the genus Tochinaiso.
[0026] まず、トチナイソゥ属植物の各作用を評価するための試験について示す。各試験に は、アンドロサセ 'エレシァの全草を製造例 1により抽出したものを用いた。  [0026] First, a test for evaluating each action of a plant of the genus Tochina is described. In each test, the whole plant of Androssace elecia was extracted according to Production Example 1.
[0027] <真皮線維芽細胞における細胞賦活作用の評価〉  [0027] <Evaluation of cell activation in dermal fibroblasts>
評価は、以下の手順で行った。正常ヒト真皮線維芽細胞を 1ゥエル当たり 2. 0 X 10 4個となるように 96穴マイクロプレートに播種した。播種培地には、ダルベッコ改変ィ 一ダル培地(DMEM)に 1 %のゥシ胎児血清を添加したものを用いた。 24時間培養 後、任意の濃度の試料を添加した試験培地に交換し、さらに 48時間培養した。次い で 3— (4, 5 ジメチルー 2 チアゾリル )ー2, 5 ジフエニルテトラゾリゥムブロミド(M TT)を 400 g/mL含有する培地に交換して 2時間培養し、テトラゾリゥム環の開環 により生じるフオルマザンを 2—プロパノールにて抽出し、マイクロプレートリーダーに て 550nmの吸光度を測定した。同時に濁度として 650nmにおける吸光度を測定し 、両測定値の差により細胞賦活作用を評価した。評価結果を、試料無添加のブラン クにおける細胞賦活作用を 100とした相対値にて表 1に示す。なお、表中の **は、 t 検定における有意確率 P値に対し、有意確率 1 %未満(P< 0. 01)を表したものであ The evaluation was performed according to the following procedure. Normal human dermal fibroblasts were seeded in a 96-well microplate at 2.0 × 10 4 cells per well. The seeding medium contains Dulbecco's modified One dull medium (DMEM) supplemented with 1% fetal bovine serum was used. After culturing for 24 hours, the medium was replaced with a test medium to which a sample of an arbitrary concentration was added, and further cultured for 48 hours. Next, replace the medium with 400 g / mL of 3- (4,5 dimethyl-2 thiazolyl) -2,5 diphenyltetrazolium bromide (MTT) and incubate for 2 hours to open the tetrazolium ring. The formazan produced by the extraction was extracted with 2-propanol, and the absorbance at 550 nm was measured with a microplate reader. At the same time, the absorbance at 650 nm was measured as turbidity, and the cell activation action was evaluated by the difference between the two measured values. The evaluation results are shown in Table 1 as relative values with the cell activation effect in the blank with no sample taken as 100. In the table, ** indicates a significance probability of less than 1% (P <0.01) with respect to significance P value in t test.
[表 1] [table 1]
Figure imgf000007_0001
Figure imgf000007_0001
[0029] 表 1より明らかなように、トチナイソゥ属植物の抽出物を添加した培地では、有意な 真皮線維芽細胞賦活作用が認められた。 [0029] As is clear from Table 1, a significant dermal fibroblast activation effect was observed in the medium supplemented with the extract of the genus Tochinaiso.
[0030] <表皮細胞における細胞賦活作用の評価〉  [0030] <Evaluation of cell activation in epidermal cells>
評価は、以下の手順で行った。正常ヒト表皮細胞を 1ゥエル当たり 2. 0 X 104個とな るように 96穴マイクロプレートに播種した。播種培地には、市販のクラボウ社製 Hume dia— KG2を用いた。 24時間培養後、試料を添加した試験培地に交換し、さらに 24 時間培養した。次いで 3— (4, 5 ジメチル 2 チアゾリル ) 2, 5 ジフエニルテトラ ゾリゥムブロミド (MTT)を 100 g/mL含有する培地に交換して 2時間培養し、テト ラゾリウム環の開環により生じるフオルマザンを 2—プロパノールにて抽出し、マイクロ プレートリーダーにて 550nmの吸光度を測定した。同時に濁度として 650nmにおけ る吸光度を測定し、両測定値の差により細胞賦活作用を評価した。評価結果を試料 が無添加の場合の細胞賦活作用を 100とした場合の相対値にて表 2に示す。 [0031] [表 2] The evaluation was performed according to the following procedure. Normal human epidermis cells were seeded in 96-well microplates at 2.0 × 10 4 cells per well. Commercially available Hume dia-KG2 manufactured by Kurabo Industries was used as the seeding medium. After culturing for 24 hours, the medium was replaced with the test medium to which the sample was added, and further cultured for 24 hours. Subsequently, the medium containing 100 g / mL of 3- (4,5 dimethyl 2 thiazolyl) 2,5 diphenyltetrazolium bromide (MTT) was exchanged and cultured for 2 hours. And the absorbance at 550 nm was measured with a microplate reader. At the same time, the absorbance at 650 nm was measured as turbidity, and the cell activation action was evaluated by the difference between the two measured values. The evaluation results are shown in Table 2 as relative values when the cell activation effect when no sample is added is 100. [0031] [Table 2]
Figure imgf000008_0001
Figure imgf000008_0001
[0032] 表 2より明らかなように、トチナイソゥ属植物の抽出物を添加した培地では、有意な 表皮細胞賦活作用が認められた。 [0032] As is clear from Table 2, a significant epidermal cell activation effect was observed in the medium to which the extract of the plant of the genus Tochina was added.
[0033] <表皮メラニン細胞におけるチロシナーゼ活性阻害作用の評価〉  [0033] <Evaluation of Tyrosinase Activity Inhibitory Action in Epidermal Melanocytes>
評価は以下の手順で行った。クラボウ社製正常ヒト表皮メラニン細胞を 1ゥエル当り 3 . 0 X 104個となるように 96穴マイクロプレートに播種した。播種培地にはクラボウ社製 Mediuml 54Sを用いた。 24時間後に各濃度の試料を添加した培地に交換し、さら に 48時間培養した。次に 1重量%1¾101 — X含有リン酸緩衝液 75 Lに交換し細 胞を完全に溶解させ内 50 Lを粗酵素液として使用した。粗酵素液に基質となる 50 li UDO. 05重量%し ドーパ含有リン酸緩衝液を加え、 37°Cで 2時間静置した。マ イク口プレートリーダーにて基質添加直後と反応終了時の 405nmの吸光度を測定し 、生成されたドーノ メラニン量を算出した。試料のチロシナーゼ活性阻害率を、試料 無添加のブランクにおけるチロシナーゼ活性阻害率に対する相対値にて表 3に示し た。 The evaluation was performed according to the following procedure. Normal human epidermal melanocytes manufactured by Kurabo Industries Co., Ltd. were seeded in a 96-well microplate so that there were 3.0 × 10 4 cells per well. As a seeding medium, Mediuml 54S manufactured by Kurabo Industries was used. After 24 hours, the medium was replaced with a medium containing each concentration of sample, and the cells were further cultured for 48 hours. Next, the solution was replaced with 75 L of 1 wt% 1¾101-X-containing phosphate buffer to completely dissolve the cells, and 50 L was used as a crude enzyme solution. The crude enzyme solution was added with 50 li UDO. 05% by weight as a substrate and a phosphate buffer solution containing dopa, and allowed to stand at 37 ° C. for 2 hours. The absorbance at 405 nm was measured immediately after the addition of the substrate and at the end of the reaction with a microphone plate reader, and the amount of produced doonomelanin was calculated. Table 3 shows the tyrosinase activity inhibition rate of the sample as a relative value to the tyrosinase activity inhibition rate in the blank with no sample added.
[0034] [表 3]  [0034] [Table 3]
Figure imgf000008_0002
Figure imgf000008_0002
[0035] 表 3より明らかなように、トチナイソゥ属植物の抽出物を添加した培地を用いた場合 には、優れたチロシナーゼ活性阻害作用が認められた。 [0035] As is apparent from Table 3, when a medium supplemented with an extract of a Tochina plant was used, an excellent inhibitory effect on tyrosinase activity was observed.
[0036] < DPPHラジカル消去による抗酸化作用の評価〉 [0036] <Evaluation of antioxidant effect by scavenging DPPH radicals>
評価は、以下の手順で行った。 50重量%エタノール水溶液にて任意の濃度に希 釈したトチナイソゥ属植物の抽出物溶液を 96穴マイクロプレートに 100 L添加した 。次に、 0. 2mMの濃度になるようにエタノールにて調製した 1、 1ージフエ二ルー 2— ピクリルヒドラジノレ (DPPH)溶液を 96穴マイクロプレートに 100 L添加した。攪拌し ながら喑所に放置し、 24時間後に 516nmの吸光度を測定した。試料が無添加のブ ランクの吸光度を (A)、試料を添加したときの吸光度を (B)としたとき、式(1)の値をラ ジカル消去率とした。評価結果を表 4に示した。 The evaluation was performed according to the following procedure. 100 L of a solution of an extract of a Tochina genus plant diluted to an arbitrary concentration with a 50% by weight aqueous ethanol solution was added to a 96-well microplate. . Next, 100 L of 1,1-diphenyl-2-picrylhydrazinole (DPPH) solution prepared in ethanol to a concentration of 0.2 mM was added to a 96-well microplate. The mixture was left standing in a place with stirring, and the absorbance at 516 nm was measured after 24 hours. When the absorbance of the blank to which the sample was not added was (A) and the absorbance when the sample was added was (B), the value of equation (1) was the radial elimination rate. The evaluation results are shown in Table 4.
式 (1) { 1 - (B) / (A) } X 100 (%)  Formula (1) {1-(B) / (A)} X 100 (%)
[表 4]  [Table 4]
Figure imgf000009_0001
Figure imgf000009_0001
[0038] 表 4より明らかなように、トチナイソゥ属植物の抽出物はラジカル消去に基づく抗酸 化作用を有することが分力、つた。 [0038] As is apparent from Table 4, it was found that the extract of the plant of the genus Tochinaiso has an antioxidant effect based on radical scavenging.
[0039] 続いて、本発明に係るトチナイソゥ属植物の抽出物を配合した皮膚外用剤と食品の 処方例を示す。 [0039] Subsequently, a formulation example of a topical skin preparation and a food containing the extract of the plant of the genus Tochina is related to the present invention.
[0040] [処方例 1]乳液 [0040] [Prescription Example 1] Emulsion
10. 0 (重量%)  10. 0 (% by weight)
エ サン 4. 0  Esang 4.0
(3)水素添加パーム核油 0. 5  (3) Hydrogenated palm kernel oil 0.5
(4)水素添加大豆リン脂質 0. 1  (4) Hydrogenated soybean phospholipid 0.1
(5)モノステアリン酸ポリオキシエチレン  (5) Polyoxyethylene monostearate
ソルビタン(20Ε· O. ) 3  Sorbitan (20Ε · O.) 3
0  0
4. 0  4. 0
(8)パラォキシ安息香酸メチル 0. 1  (8) Methyl paraoxybenzoate 0.1
(9)カノレポキシビニノレポリマー 0. 15  (9) Canolepoxy bininole polymer 0.15
(10)精製水 57. 85  (10) Purified water 57. 85
重量%水溶液) 20. 0 '属植物の抽出物 [製造例 1] (Wt% aqueous solution) 20. 0 'Extract of genus plant [Production Example 1]
製法:(1)〜½)の油相成分を 80°Cにて加熱溶解する。一方(7)〜(10)の水相成分 を 80°Cにて加熱溶解する。これに前記油相成分を攪拌しながら加え、ホモジナイザ 一により均一に乳化する。乳化終了後、冷却を開始し、(11)と(12)を順次加え、均一 に混合する。 Production method: The oil phase components (1) to ½) are heated and dissolved at 80 ° C. On the other hand, the aqueous phase components (7) to (10) are heated and dissolved at 80 ° C. The oil phase component is added to this while stirring and uniformly emulsified with a homogenizer. After emulsification, start cooling and add (11) and (12) sequentially and mix evenly.
[処方例 2]化粧水  [Prescription Example 2] Lotion
(1)エタノール 15· 0 (重量0 /0) (1) ethanol 15 - 0 (weight 0/0)
(2)ポリオキシエチレン(40Ε· Ο. )硬化ヒマシ油 0· 3  (2) Polyoxyethylene (40Ε · Ο.) Hardened castor oil 0 · 3
(3)香料 0. 1  (3) Fragrance 0. 1
(4)精製水 82. 38
Figure imgf000010_0001
Figure imgf000010_0002
(4) Purified water 82. 38
Figure imgf000010_0001
Figure imgf000010_0002
(9)トチナイソゥ属植物の抽出物 [製造例 3]  (9) Extracts of Tochinaiso plant [Production Example 3]
製法:(1)に(2)及び(3)を溶解する。溶解後、(4)〜(8)を順次添加した後、十分に 攪拌し、(9)を加え、均一に混合する。 Production method: Dissolve ( 2 ) and (3) in (1). After dissolution, sequentially add ( 4 ) to (8), then stir well, add (9), and mix uniformly.
[処方例 3]クリーム  [Prescription Example 3] Cream
10. 0 (重量%)  10. 0 (% by weight)
2. 0  2. 0
(3)水素添加パーム核油 0. 5  (3) Hydrogenated palm kernel oil 0.5
(4)水素添加大豆リン脂質 0. 1  (4) Hydrogenated soybean phospholipid 0.1
—ノレ 3. 6  —Nore 3.6
½)親油型 2. 0  ½) Lipophilic type 2.0
10. 0  10. 0
(8)パラォキシ安息香酸メチル 0. 1  (8) Methyl paraoxybenzoate 0.1
(9)アルギニン (20重量%水溶液) 15. 0  (9) Arginine (20 wt% aqueous solution) 15. 0
(10)精製水 40. 7 (11)カルボキシビュルポリマー(1重量%水溶液) 15· 0 (10) Purified water 40.7 (11) Carboxybule polymer (1 wt% aqueous solution) 15 · 0
(12)トチナイソゥ属植物の抽出物 [製造例 1] 1. 0  (12) Tochinaiso plant extract [Production Example 1] 1.0
製法:(1)〜½)の油相成分を 80°Cにて加熱溶解する。一方(7)〜(10)の水相成分 を 80°Cにて加熱溶解する。これに前記油相成分を攪拌しながら加え、ホモジナイザ 一により均一に乳化する。乳化終了後、(11)を加え、冷却を開始し、 40°Cにて(12) を加え、均一に混合する。 Production method: The oil phase components (1) to ½) are heated and dissolved at 80 ° C. On the other hand, the aqueous phase components (7) to (10) are heated and dissolved at 80 ° C. The oil phase component is added to this while stirring and uniformly emulsified with a homogenizer. After emulsification, add (11), start cooling, add (12) at 40 ° C and mix uniformly.
[処方例 4]美容液  [Prescription Example 4] Essence
(1)精製水 27· 45(重量%)  (1) Purified water 27-45 (wt%)
(2)グリセリン 14· 0  (2) Glycerin 14
(3)ショ糖脂肪酸エステル 1. 3  (3) Sucrose fatty acid ester 1.3
(4)カルボキシビュルポリマー(1重量%水溶液) 17· 5  (4) Carboxybule polymer (1 wt% aqueous solution) 17 · 5
(5)アルギン酸ナトリウム (1重量%水溶液) 15· 0  (5) Sodium alginate (1 wt% aqueous solution) 15 · 0
(6)モノラウリン酸ポリグリセリル 1 · 0  (6) Polyglyceryl monolaurate 1
(7)マカデミアナッツ油脂肪酸フィトステリノレ 3· 0  (7) Macadamia nut oil fatty acid phytosterinole 3.0
(8) N-ラウロイル -L-グルタミン酸  (8) N-lauroyl-L-glutamic acid
ジ(フィトステリルー2—オタチルドデシル) 2· 0  Di (Phytosteril 2—Otachidodecyl) 2 · 0
(9)硬化パーム油 2· 0  (9) Hardened palm oil 2.0
(10)スクヮラン (ォリーブ由来) 1 · 0  (10) Sukuran (Olive) 1 · 0
(11)ベへニルアルコール 0. 75  (11) Behenyl alcohol 0.75
(12)ミツロウ 1 · 0  (12) Beeswax 1 0
(13)ホホバ油 1. 0  (13) Jojoba oil1.0
(14) 1、 3—ブチレングリコール 10· 0  (14) 1, 3-butylene glycol 10 · 0
(15) L—アルギニン(10重量%水溶液) 2· 0  (15) L-Arginine (10 wt% aqueous solution) 2 · 0
(16)トチナイソゥ属植物の抽出物 [製造例 1] 1. 0  (16) Extracts of plants belonging to the genus Tochina [Production Example 1] 1.0
製法:(1)〜½)の水相成分を混合し、 75°Cにて加熱溶解する。一方、(7)〜(14)の 油相成分を混合し、 75°Cにて加熱溶解する。次いで、上記水相成分に油相成分を 添加して予備乳化を行った後、ホモミキサーにて均一に乳化する。乳化終了後に冷 却を開始し、 50°Cにて(15)を加える。さらに 40°Cまで冷却し、(16)を加え、均一に混 合する。 Production method: The aqueous phase components (1) to ½) are mixed and dissolved by heating at 75 ° C. On the other hand, the oil phase components (7) to (14) are mixed and dissolved by heating at 75 ° C. Next, the oil phase component is added to the aqueous phase component and preliminary emulsification is performed, followed by uniform emulsification with a homomixer. Start cooling after emulsification and add (15) at 50 ° C. Cool to 40 ° C and add (16) to mix evenly. Match.
[0044] [処方例 5]水性、: [0044] [Prescription Example 5] Aqueous:
(1)カノレポキシビニノレポリマー 0. 5 (重量%)  (1) Canolepoxy bininole polymer 0.5 (wt%)
(2)精製水 86· 7  (2) Purified water 86 7
(3)水酸化ナトリウム(10重量%水溶液) 0· 5  (3) Sodium hydroxide (10 wt% aqueous solution) 0 · 5
(4)エタノーノレ 10· 0  (4) Ethanore 10 · 0
(5)パラォキシ安息香酸メチル 0· 1  (5) Methyl parabenzoate 0/1
(6)香料 0· 1  (6) Fragrance 0 · 1
(7)トチナイソゥ属植物の抽出物 [製造例 4] 2. 0  (7) Extracts of Tochinaiso plants [Production Example 4] 2.0
(8)ポリオキシエチレン(60Ε· O. )硬化ヒマシ油 0· 1  (8) Polyoxyethylene (60Ε · O.) Hydrogenated castor oil 0 · 1
製法:(1)を(2)に加え、均一に攪拌した後、(3)を加える。均一に攪拌した後、(4) に予め溶解した(5)を加える。均一に攪拌した後、予め混合しておいた(6)〜(8)を 加え、均一に攪拌混合する。  Production method: Add (1) to (2), stir uniformly, and then add (3). After stirring uniformly, add (5) previously dissolved in (4). After stirring uniformly, add (6) to (8) previously mixed and stir and mix uniformly.
[0045] [処方例 6]クレンジング料 [0045] [Prescription Example 6] Cleansing Fee
(1)スクヮラン 81 · 0 (重量0 /0) (1) Sukuwaran 81 and 0 (weight 0/0)
(2)イソステアリン酸ポリオキシエチレングリセリル 15· 0  (2) Polyoxyethylene glyceryl isostearate 15
(3)精製水 3· 0  (3) Purified water 3
(4)トチナイソゥ属植物の抽出物 [製造例 4] 1. 0  (4) Extracts of plants belonging to the genus Tochina [Production Example 4] 1.0
製法:(1)と(2)を均一に溶解する。これに、(3)と (4)を順次加え、均一に混合する。  Production method: Dissolve (1) and (2) uniformly. Add (3) and (4) to this, and mix evenly.
[0046] [処方例 7]洗顔フォーム [0046] [Prescription Example 7] face washing foam
16. 0 (重量%)  16. 0 (wt%)
(2)ミリスチン酸 16. 0  (2) Myristic acid 16.0
(3)親油型 2. 0  (3) Lipophilic type 2.0
20. 0  20. 0
(5)水酸 7. 5  (5) Hydroxide 7.5
(6)ヤシ油脂肪酸ァ 1. 0  (6) Palm oil fatty acid 1.0
(7)精製水 36. 5  (7) Purified water 36.5
(8)トチナイソゥ属植物の抽出物 [製造例 3] 1. 0 製法:(1)〜(4)の油相成分を 80°Cにて加熱溶解する。一方(5)〜(7)の水相成分 を 80°Cにて加熱溶解し、油相成分と均一に混合撹拌する。冷却を開始し、 40°Cにて (8)を加え、均一に混合する。 (8) Tochinaiso plant extract [Production Example 3] 1.0 Production method: The oil phase components (1) to (4) are heated and dissolved at 80 ° C. On the other hand, the water phase components (5) to (7) are heated and dissolved at 80 ° C, and the oil phase components are mixed and stirred uniformly. Start cooling, add (8) at 40 ° C, and mix uniformly.
[0047] [処方例 8]メイクアップベースクリーム  [0047] [Prescription Example 8] Makeup base cream
10. 0(重量%)  10. 0 (wt%)
ノレ 2. 0  Nore 2.0
(3)グリセリントリー 2—ェチルへキサン酸エステル 2· 5  (3) Glycerol tree 2-ethyl hexanoate 2.5
(4)親油型 0  (4) Lipophilic type 0
:π一ノレ 11. 0  : π
(6)ショ糖脂肪酸 3  (6) Sucrose fatty acid 3
(7)精製水 69. 4  (7) Purified water 69.4
(8)酸化チタン 0  (8) Titanium oxide 0
(9)ベンガラ 0.  (9) Bengala 0.
(10)黄酸化鉄 0. 4  (10) Yellow iron oxide 0.4
(11)香料 0. 1  (11) Fragrance 0. 1
'属植物の抽出物 [製造例 2] 1. 2  'Extract of genus plant [Production Example 2] 1.2
製法:(1)〜(4)の油相成分を混合し、 75°Cにて加熱溶解する。一方、(5)〜(7)の 水相成分を混合し、 75°Cにて加熱溶解し、これに(8)〜(10)の顔料を加え、ホモミキ サ一にて均一に分散させる。この水相成分に前記油相成分を加え、ホモミキサーに て乳化する。乳化終了後に冷却を開始し、 40°Cにて(11)と(12)の成分を加え、均一 に混合する。  Production method: The oil phase components (1) to (4) are mixed and dissolved by heating at 75 ° C. On the other hand, the aqueous phase components (5) to (7) are mixed, dissolved by heating at 75 ° C, and the pigments (8) to (10) are added thereto and dispersed uniformly with a homomixer. The oil phase component is added to the water phase component and emulsified with a homomixer. Start cooling after emulsification, add ingredients (11) and (12) at 40 ° C and mix evenly.
[0048] [処方例 9]乳液状:  [0048] [Prescription Example 9] Emulsion:
サン 2. 0(重量%)  Sun 2.0 (wt%)
5. 0  5. 0
(3)ミリスチン酸; 5. 0  (3) Myristic acid; 5.0
一ノレ 1. 0  One point 1. 0
(5)ポリオキシエチレン (20Ε· O. )  (5) Polyoxyethylene (20Ε ・ O.)
3 0. 7 Three 0. 7
(7) 1、 3—ブチレングリコール 8. 0  (7) 1, 3-Butylene glycol 8.0
(8)キサンタンガム 0. 1  (8) Xanthan gum 0.1
(9)パラォキシ安息香酸メチル 0.  (9) Methyl paraoxybenzoate 0.
(10)精製水 57. 4  (10) Purified water 57.4
(11)酸ィ 9. 0  (11) Acid 9.0
7. 4  7. 4
(13)ベンガラ 0. 5  (13) Bengala 0.5
(14)黄酸化鉄  (14) Yellow iron oxide
(15)黒酸化鉄 0. 1  (15) Black iron oxide 0.1
(16)香料 0. 1  (16) Fragrance 0. 1
'属植物の抽出物 [製造例 4] 1. 0  'Extract of genus plant [Production Example 4] 1.0
製法:(1)〜½)の油相成分を混合し、 75°Cにて加熱溶解する。一方、(7)〜(10)の 水相成分を混合し、 75°Cにて加熱溶解し、これに(11)〜(15)の顔料を加え、ホモミ キサ一にて均一に分散する。油相成分を加え、乳化を行う。乳化終了後に冷却を開 始し、 40°Cにて(16)と(17)の成分を順次加え、均一に混合する。 Production method: The oil phase components (1) to ½) are mixed and dissolved by heating at 75 ° C. On the other hand, the water phase components (7) to (10) are mixed, dissolved by heating at 75 ° C, and the pigments (11) to (15) are added to this and dispersed uniformly with a homomixer. Add oil phase ingredients and emulsify. Cooling is started after emulsification, and components (16) and (17) are added sequentially at 40 ° C and mixed uniformly.
[処方例 10]油中水型ェモリエントクリーム  [Prescription Example 10] Water-in-oil emollient cream
(1)流動ノ 30. 0(重量0 /0) (1) Current Roh 30.0 (weight 0/0)
2. 0  2. 0
5. 0  5. 0
5. 0  5. 0
(5)塩化ナトリウム 1. 3  (5) Sodium chloride 1.3
(6)塩化カリウム 0. 1  (6) Potassium chloride 0.1
):π—ノレ 3. 0  ): π—Nore 3.0
(8) 1、 3—ブチレングリコール 5. 0  (8) 1, 3-butylene glycol 5.0
(9)パラォキシ安息香酸メチル 0. 1  (9) Methyl paraoxybenzoate 0.1
(10)トチナイソゥ属植物の抽出物 [製造例 1] 1. 0  (10) Extracts of Tochinais [Manufacturing Example 1] 1.0
(11)精製水 47. 4 (12)香料 (11) Purified water 47.4 (12) Fragrance
製法:(5)と(6)を(11)の一部に溶解して 50°Cとし、 50°Cに加熱した (4)に撹拌しな がら徐々に加える。これを混合した後、 70°Cにて加熱溶解した(1)〜(3)に均一に分 散する。これに(7)〜(10)を(11)の残部に 70°Cにて加熱溶解したものを撹拌しなが ら加え、ホモミキサーにて乳化する。乳化終了後に冷却を開始し、 40°Cにて(12)を 加え、均一に混合する。  Manufacturing method: Dissolve (5) and (6) in a part of (11) to 50 ° C, and gradually add to (4) heated to 50 ° C while stirring. After mixing this, disperse uniformly into (1) to (3), which is heated and dissolved at 70 ° C. Add (7) to (10), which is dissolved in the remainder of (11) by heating at 70 ° C while stirring, and emulsify with a homomixer. Start cooling after emulsification, add (12) at 40 ° C, and mix evenly.
[0050] [処方例 11]パック  [0050] [Prescription Example 11] Pack
(1)精製水 62· 9(重量%)  (1) Purified water 62.9 (wt%)
(2)ポリビュルアルコール 12· 0  (2) Polybule alcohol 12.0
(3)エタノール 17· 0  (3) Ethanol 17
(4)グリセリン 5. 0  (4) Glycerin 5.0
(5)ポリエチレングリコール(平均分子量 1000) 2· 0  (5) Polyethylene glycol (average molecular weight 1000) 2 · 0
(6)トチナイソゥ属植物の抽出物 [製造例 2] 1. 0  (6) Tochinaiso plant extract [Production Example 2] 1.0
(7)香料 0. 1  (7) Fragrance 0. 1
製法:(2)と(3)を混合し、 80°Cに加温した後、 80°Cに加温した(1)に溶解する。均 一に溶解した後、(4)と(5)を加え、攪拌しながら冷却を開始する。 40°Cまで冷却し、 (6)と (7)を加え、均一に混合する。  Manufacturing method: (2) and (3) are mixed, heated to 80 ° C, and then dissolved in (1) heated to 80 ° C. After evenly dissolving, add (4) and (5) and start cooling with stirring. Cool to 40 ° C, add (6) and (7), and mix evenly.
[0051] [処方例 12]入浴剤  [0051] [Prescription Example 12] Bath salt
(1)香料 0· 3(重量%)  (1) Fragrance 0-3 (% by weight)
(2)トチナイソゥ属植物の抽出物 [製造例 1] 1. 0  (2) Tochinaiso plant extract [Production Example 1] 1.0
(3)炭酸水素ナトリウム 50. 0  (3) Sodium bicarbonate 50. 0
(4)硫酸ナトリウム 48. 7  (4) Sodium sulfate 48.7
製法:(1)〜(4)を均一に混合する。  Production method: (1) to (4) are mixed uniformly.
[0052] [処方例 13]ヘアーワックス  [0052] [Prescription Example 13] Hair wax
3. 0(重量%) 3. 0 (% by weight)
Figure imgf000015_0001
Figure imgf000015_0001
(3)セチルアルコール  (3) Cetyl alcohol
(4)高重合メチルポリシロキサン -サン 5· 0 メチルポリシロキサン共重合体 1. 0 (4) Highly polymerized methylpolysiloxane -Sun 5.0 methylpolysiloxane copolymer 1.0
(7)パラォキシ安息香酸メチル 0· 1  (7) Methyl parabenzoate 0/1
(8) 1、 3—ブチレングリコール 7. 5  (8) 1,3-Butylene glycol 7.5
(9)アルギニン 0· 7  (9) Arginine 0-7
(10)精製水 74· 6  (10) Purified water 74
(11)トチナイソゥ属植物の抽出物 [製造例 1] 1. 0  (11) Extracts of Tochinais [Manufacturing Example 1] 1.0
(12)香料 0. 1  (12) Fragrance 0. 1
製法:(1)〜½)の油相成分を混合し、 75°Cにて加熱溶解後する。一方、(7)〜(10) の水相成分を 75°Cにて加熱溶解し、前記油相成分を加え、ホモミキサーにて乳化す る。乳化終了後に冷却を開始し、 40°Cにて(11)と(12)の成分を加え、均一に混合す  Production method: The oil phase components (1) to ½) are mixed and heated and dissolved at 75 ° C. On the other hand, the aqueous phase components (7) to (10) are dissolved by heating at 75 ° C, and the oil phase component is added and emulsified with a homomixer. Start cooling after emulsification, add ingredients (11) and (12) at 40 ° C and mix evenly
[0053] [処方例 14]ヘアートニック [0053] [Prescription Example 14] Hair art nick
(1)エタノール 50· 0(重量0 /0) (1) Ethanol 50 - 0 (wt 0/0)
(2)精製水 48· 9  (2) Purified water 48 9
(3)トチナイソゥ属植物の抽出物 [製造例 3] 1. 0  (3) Tochinaiso plant extract [Production Example 3] 1.0
(4)香料 0· 1  (4) Fragrance 0 · 1
製法:(1)〜(4)の成分を混合、均一化する。  Production method: Components (1) to (4) are mixed and homogenized.
[0054] [処方例 15]錠剤  [0054] [Prescription Example 15] Tablet
(1)トチナイソゥ属植物の抽出物 [製造例 1] 100. 0 (mg)  (1) Extract of Tochinais [Manufacturing Example 1] 100. 0 (mg)
(2)還元麦芽糖水飴 461. 0  (2) Reduced maltose starch syrup 461.0
(4)グリセリン脂肪酸エステル 12. 0 (4) Glycerin fatty acid ester 12.0
(5)香料 12· 0  (5) Fragrance 12 0
製法:(1)〜(3)をそれぞれ篩過して混合し、次いで、(4)〜(5)を添加して混合した 。その後、常法により打錠して、全量が 600mgの錠剤を得た。  Production method: (1) to (3) were respectively sieved and mixed, and then (4) to (5) were added and mixed. Thereafter, tableting was performed by a conventional method to obtain a tablet having a total amount of 600 mg.
[0055] 次に、トチナイソゥ属植物の抽出物を配合した処方を用いて使用試験を行い、乾燥 による肌荒れについて改善効果を評価した。その際、処方例 1に示した乳液の処方 に表 5に記載するトチナイソゥ属植物の抽出物をそれぞれ配合し、実施例 1〜2として 使用試験を行った。また、トチナイソゥ属植物の抽出物を精製水に代替し、比較例 1 として同時に使用試験を行った。 [0055] Next, a use test was conducted using a formulation formulated with an extract of a plant of the genus Tochina, and dried. The improvement effect was evaluated for rough skin. At that time, the extract of the plant belonging to the genus Tochinaiso listed in Table 5 was added to the formulation of the emulsion shown in Formulation Example 1, and the use test was conducted as Examples 1-2. Moreover, the extract of the plant of the genus Tochina is replaced with purified water, and a use test was simultaneously conducted as Comparative Example 1.
[表 5]
Figure imgf000017_0001
[Table 5]
Figure imgf000017_0001
[0057] 各試料について、肌荒れ症状が顕著に認められる 30〜50才代の乾燥肌の女性パ ネラー 20名をそれぞれ一群とし、ブラインドにて 1週間使用させ、使用前後の皮膚状 態の変化を観察して評価した。皮膚症状の指標として、乾燥による肌荒れについて、 「改善」、「やや改善」、「変化なし」の三段階で評価し、表 6に各評価を得たパネラー 数にて示した。 [0057] For each sample, a group of 20 female panelists with dry skin in their 30s to 50s who had markedly rough skin symptoms, and used blinds for 1 week to change the skin condition before and after use. Observed and evaluated. As an index of skin symptoms, rough skin due to dryness was evaluated in three stages: “Improved”, “Slightly improved”, and “No change”, and Table 6 shows the number of panelists that obtained each evaluation.
[0058] [表 6]
Figure imgf000017_0002
[0058] [Table 6]
Figure imgf000017_0002
[0059] 表 6より、トチナイソゥ属植物の抽出物は優れた保湿効果を有することが明ら力、とな つた。 [0059] From Table 6, it has become clear that the extract of the genus Tochinaiso has an excellent moisturizing effect.
産業上の利用可能性  Industrial applicability
[0060] 本発明の保湿剤、細胞賦活剤、美白剤、及び抗酸化剤は、皮膚外用剤、食品、医 薬品、医薬部外品に配合して用いるのに有用である。なお、本発明に係るトチナイソ ゥ属植物の抽出物は、天然由来の成分であることもあり、皮膚外用剤及び食品の素 材としての意義も大きぐしたがって本発明は、新たな皮膚外用剤及び食品として有 用である。 [0060] The humectant, cell activator, whitening agent, and antioxidant of the present invention are useful for blending into skin external preparations, foods, pharmaceuticals, and quasi drugs. In addition, the extract of the plant of the genus Tochinacea according to the present invention may be a component derived from nature and has great significance as a skin external preparation and a food ingredient. Useful as food.

Claims

請求の範囲 The scope of the claims
[1] トチナイソゥ属植物より選ばれる 1種又は 2種以上の植物の抽出物を有効成分とす る保湿剤。  [1] A moisturizing agent containing as an active ingredient an extract of one or more plants selected from plants belonging to the genus Tochinaiso.
[2] トチナイソゥ属植物より選ばれる 1種又は 2種以上の植物の抽出物を有効成分とす る細胞賦活剤。  [2] A cell activator comprising, as an active ingredient, an extract of one or more plants selected from plants belonging to the genus Tochinaiso.
[3] トチナイソゥ属植物より選ばれる 1種又は 2種以上の植物の抽出物を有効成分とす る美白剤。  [3] A whitening agent comprising, as an active ingredient, an extract of one or more plants selected from plants belonging to the genus Tochinaiso.
[4] トチナイソゥ属植物より選ばれる 1種又は 2種以上の植物の抽出物を有効成分とす る抗酸化剤。  [4] An antioxidant comprising, as an active ingredient, an extract of one or more plants selected from plants belonging to the genus Tochinaiso.
[5] トチナイソゥ属植物より選ばれる 1種又は 2種以上の植物の抽出物を含有する皮膚 外用剤。  [5] An external preparation for skin containing an extract of one or more plants selected from plants belonging to the genus Tochinaiso.
[6] トチナイソゥ属植物より選ばれる 1種又は 2種以上の植物の抽出物を含有する食品  [6] Food containing an extract of one or more plants selected from plants belonging to the genus Tochinaiso
PCT/JP2007/068126 2006-09-20 2007-09-19 Moisturizing agent, cell-activating agent, skin-whitening agent, and antioxidant agent WO2008035691A1 (en)

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WO2004087820A1 (en) * 2003-03-31 2004-10-14 Matsushita Electric Industrial Co. Ltd. Insect repellent coating and industrial product using the same
JP2006016334A (en) * 2004-07-01 2006-01-19 Noevir Co Ltd Moisturizer, cell-activating agent, beautifully whitening agent, antioxidant and skin preparation for external use
JP2006063056A (en) * 2004-08-30 2006-03-09 Noevir Co Ltd Humectant, cell-activating agent, bleaching agent and antioxidant

Patent Citations (3)

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Publication number Priority date Publication date Assignee Title
WO2004087820A1 (en) * 2003-03-31 2004-10-14 Matsushita Electric Industrial Co. Ltd. Insect repellent coating and industrial product using the same
JP2006016334A (en) * 2004-07-01 2006-01-19 Noevir Co Ltd Moisturizer, cell-activating agent, beautifully whitening agent, antioxidant and skin preparation for external use
JP2006063056A (en) * 2004-08-30 2006-03-09 Noevir Co Ltd Humectant, cell-activating agent, bleaching agent and antioxidant

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Title
TSEVEGSUREN N. ET AL.: "Isomers of hexadecenoic and hexadecadienoic acids in Androsace septentrionalis (Primulacae) seed oil", LIPIDS, vol. 38, no. 11, November 2003 (2003-11-01), pages 1173 - 1178, XP003021838 *

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