WO2004075621A2 - 抗老化剤およびコラーゲン産生促進剤 - Google Patents
抗老化剤およびコラーゲン産生促進剤 Download PDFInfo
- Publication number
- WO2004075621A2 WO2004075621A2 PCT/JP2004/007038 JP2004007038W WO2004075621A2 WO 2004075621 A2 WO2004075621 A2 WO 2004075621A2 JP 2004007038 W JP2004007038 W JP 2004007038W WO 2004075621 A2 WO2004075621 A2 WO 2004075621A2
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- WIPO (PCT)
- Prior art keywords
- hydrolyzate
- hydrogen peroxide
- collagen
- animal
- production
- Prior art date
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Classifications
-
- 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
- A61K8/99—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from microorganisms other than algae or fungi, e.g. protozoa or bacteria
-
- 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
- A61K8/9728—Fungi, e.g. yeasts
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/08—Anti-ageing preparations
Definitions
- the present invention relates to an anti-aging agent and a collagen production promoter, and more particularly, to an anti-aging agent which promotes the production of collagen, which is one of extracellular matrix components.
- the present invention relates to an aging agent and a collagen production promoter.
- the present invention relates to collagen gel shrinkage, fibroblast or epidermal cell integrins.
- the present invention relates to an agent and a method for promoting production.
- natural components derived from natural products that promote and prevent collagen from aging by promoting collagen production include, for example, isoflavones selected from daidizin, daizudin, genistin, and genistin
- the compound phytosterol has been reported (see Patent Document 1.
- the present inventors have conducted intensive research on a substance having an action of strongly promoting collagen biosynthesis of skin fibroblasts, and as a result, a hydrogen peroxide-treated yeast hydrolyzate cultured in a specific nutrient medium promotes collagen production.
- the present invention provides an anti-aging agent, which comprises a collagen production promoter containing a hydrolyzate of a hydrogen peroxide-treated yeast cultured in a nutrient medium containing non-animal-derived glycosaminoglycan as an active ingredient,
- a collagen production promoter characterized by containing, as an active ingredient, a hydrolyzate of a hydrogen peroxide-treated yeast cultured in a nutrient medium containing glycosaminoglycans derived from non-animals, and a hydrogen peroxide-treated yeast hydrolyzate It is intended to provide a method for promoting the production of collagen, which is characterized in that the production of collagen is promoted using the same.
- the hydrogen peroxide-treated yeast hydrolyzate used in the present invention has an elastin production promoting effect, but it has not been known that it has a collagen production promoting effect. It was found.
- having an elastin production promoting effect and having a collagen production promoting effect are different technical matters, and having an elastin production promoting effect means that having an elastin production promoting effect has a collagen production promoting effect. Not necessarily.
- the present inventor has proposed that the hydrogen peroxide-treated yeast hydrolyzate is used to prevent skin aging, for example, contraction of collagen gel, which is known to be involved in prevention and improvement of wrinkles and sagging, and promotion of integrin production by skin cells. Further examination of the results shows that, surprisingly, this hydrolyzate has an effect of promoting the contraction of collagen gel, an effect of promoting the production of integrin by fibroblasts, and particularly an effect of integrin ⁇ 2, a3, a.
- the present invention is characterized in that it contains a collagen gel contraction promoter containing a hydrolyzate of a hydrogen peroxide-treated yeast cultured in a nutrient medium containing non-animal-derived glycosaminoglycan as an active ingredient.
- a collagen gel shrinkage accelerator comprising, as active ingredients, a hydrolyzate of a hydrogen peroxide-treated yeast cultured in a nutrient medium containing a non-animal-derived glycosamino-nodalican;
- the present invention provides a collagen gel shrinkage promoting method characterized by promoting shrinkage of collagen gel using the hydrogen peroxide-treated yeast hydrolyzate.
- the present invention provides an integrin production promoter for fibroblasts, comprising as an active ingredient a hydrolyzate of a hydrogen peroxide-treated yeast cultured in a nutrient medium containing non-animal-derived glycosaminoglycan. It contains, as active ingredients, an anti-aging agent characterized by containing, and a hydrolyzate of a hydrogen peroxide-treated yeast cultured in a nutrient medium containing non-animal-derived glycosaminoglycan.
- the present invention relates to the promotion of integulin production of epidermal cells containing a hydrolyzate of a hydrogen peroxide-treated yeast cultured in a nutrient medium containing non-animal-derived glycosaminoglycan as an active ingredient.
- Anti-aging agent characterized by containing a hydrolyzate of a hydrogen peroxide-treated yeast cultured in a nutrient medium containing non-animal-derived glycosaminoglycan as an active ingredient.
- the hydrogen peroxide-treated yeast hydrolyzate used in the present invention is obtained by treating yeast in a hydrogen peroxide solution to obtain a water-soluble yeast hydrolyzate, and more preferably a water-soluble yeast further subjected to ultraviolet irradiation. It is a hydrolyzate.
- the details including the production method are described in U.S. Patent No. 6,461,857.
- the peracidio hydrogen-treated yeast calo-moisture fast food used in the present invention is commercially available from Arch Persone Carle Products LP, Inc. under the trade name "Piodyne EMPP (TM)".
- the hydrolyzate of the hydrogen peroxide-treated yeast of the present invention is a cytoprotective component that protects cells from stress by reacting cultured yeast cultured under stress with hydrogen peroxide under stress. It can be prepared by adding hydrogen peroxide to cultured yeast cells and culturing the cells in a nutrient medium containing non-animal-derived glycosaminoglycans.
- the hydrogen peroxide-treated yeast hydrolyzate of the present invention is, for example, It can be prepared as described:
- (B) sublethal to the culture for example, loading the stress by adding the total mass of about 0.1 to 2 mass 0/0 hydrogen peroxide in culture;
- a sublethal dose of ultraviolet light eg, UVA / UVB irradiation at an intensity of 31.5 mj Z cm 2 ;
- the water-soluble yeast extract is recovered from the culture containing hydrogen peroxide.
- the anti-aging agent, collagen production promoter, collagen gel constrictor, fibroblast integrin production promoter and epidermal cell integrin production promoter of the present invention include, in addition to the above-mentioned essential components, usually for external use in the skin of cosmetics and pharmaceuticals.
- Ingredients used in preparations for example, whitening agents, humectants, antioxidants, oily components, UV absorbers, surfactants, thickeners, alcohols, powder components, coloring materials, aqueous components, water, various skin nutrition Agents and the like can be appropriately compounded as needed.
- sequestering agents such as sodium edetate, trisodium edetate, sodium citrate, sodium polyphosphate, sodium metaphosphate, gluconate, caffeine Tannin, verapamil, tranexamic acid and its derivatives, licorice extract, glabridin, hot water extract of fire thorn fruit, various crude drugs, tocopherol acetate, glycyrrhizic acid and its derivatives or their salts, etc.
- Other whitening agents such as glucose C, magnesium ascorbyl phosphate, darcoside ascorbate, alptin, kojic acid, and sugars such as glucose, fructose, mannose, sucrose, trehalose, etc. are also appropriately added. be able to.
- the present invention is particularly suitable for cosmetics, quasi-drugs, etc. applied to the outer skin.
- Can be widely applied to cosmetics, and its dosage form is aqueous, solubilizing, emulsifying, powder, oil-liquid, gel, ointment, aerosol, water-oil two-layer,
- a wide range of dosage forms such as water-oil-powder 3-layer system can be rubbed. That is, basic cosmetics can be widely applied to the above-mentioned various dosage forms in the form of facial cleansers, lotions, milky lotions, talmes, jewels, essences (cosmetics), packs, masks and the like.
- make-up cosmetics can be widely applied to foundations and toys such as body soaps and soaps as toy products.
- quasi-drugs can be widely applied to various ointments and the like.
- the form and form of the collagen production promoter of the present invention are not limited to these forms and forms. Example. . .
- Test Example 1 Type I Collagen Atsushi
- Human fibroblasts were seeded on a 96-well plate in 1 ⁇ 10 4 cellsZwell in 10% fetal bovine serum-added DMEM medium, and the serum concentration was reduced to 0.5% after 3 to 4 hours. One day later, the cells were replaced with 0.5% serum-added DMEM medium supplemented with Biodyne EMPP at each concentration. On the fourth day after the cell seeding, the type I collagen in the culture supernatant and the amount of DNA in the cells were measured and used as an index of the cell number.
- the amount of DNA is measured by the fluorescence measurement method using Hoechst H33342 did.
- the type I procollagen C-terminal peptide (Procollagen type carboxy terminal propeptide: PIPj) produced by human fibroblasts was measured by ELISA using Kit MK_1101 manufactured by Takara Shu. The amount of PIP was measured. When the amount of PIP per DNA was 100, the amount of PIP per DNA of the added sample was defined as the type I collagen production promotion rate.
- the yeast culture hydrolyzate “Piondine TRF-25” (trade name of Arch Persona 1 Care Products LP) was used in the same manner as described above. The effect of promoting collagen production was examined.
- the method for producing “Pyodin TRF-25” does not enrich the yeast culture medium with various low molecular weight growing peptides and non-animal derived daricosaminoglycans as nutrients.
- the point that hydrogen peroxide treatment is not performed is different from the method for producing “Pyodyne EMP PJ” of the present invention.
- Test Example 2 Type VII Collagen Atsushi
- the measurement of the amount of DNA was performed by a fluorescence measurement method using Hoechst's H33342.
- Type VII collagen was measured by sandwich ELISA method.
- the antibodies used in this example are as follows.
- the group to which Biodyne EMPP was added was far superior in the type I collagen production promoting effect compared to the group to which Biodyne TRF-25 was added. Furthermore, it became clear that the group to which Biodyne EMPP was added also had a type VII collagen production promoting effect.
- yeast extract obtained by extracting the yeast with an aqueous solvent did not show any collagen production promoting effect. This result is also described in Japanese Patent No. 32781338.
- the group added with PIODINE EMPP was far superior in the collagen gel shrinkage promoting effect as compared with the control group, and its concentration dependency was also confirmed.
- Test Example 4 (Ability to promote integrin production in dermal fibroblasts)
- Pyodyne EMPP was allowed to act on human skin fibroblasts, and after 24 hours, the cells were detached with trypsin / EDTA and neutralized with FCS. % N a N 3 to recover washing said cells with containing PBS.
- Anti-human interdarin A2, a3, A6, ⁇ 2j31,; 31 were diluted 100-fold as primary antibodies, respectively, FITC-labeled anti-mouse Ig Gi was used at a 1: 100 dilution. Blank used mouse IgG1 as the primary antibody. The amount of integrins on the cell surface was measured using a FACS can.
- Test Example 5 (Attach ability to promote integrin production in epidermal cells)
- Pyodyne EMPP was allowed to act on epidermal cells (HaCaT cells), and the amount of integrins on the cell surface was measured using FACScan as in Test Example 4.
- Anti-human integrins 2, a3, a6, and 2j81,] 31, and j84 were each diluted 100-fold as the primary antibody.
- Dimethyl diste- nary ammonium hydroxide 1.5 Polyvinylenole cone 0.1 Hydroxicetinoresenorelose 0.1 Natrium acrylate / 2-acrylamide-2-methylpropanesulfonate copolymer 0
- Titanium mica 0.5 Purified water residue
- Dipropyl pyrene cornole 1. mass% decamethinoresic mouth pentasiloxane 5.
- Acrylic acid alkyl methacrylate copolymer (Dumylene TR-2) 0.05 Amyl acrylate K / 2-T acrylamide-2-methylpropanesulfonic acid copolymer 0. Five
- 1,3-butylene glycol 5.0 polyoxyethylene methyl dalcoside 3.0 sunflower oil 1.0 squalane 2.0 hydroxylating power 0.1 sodium hexamethacrylate 0.0 Five Hydroxypropyl pil j3—cyclodextrin 0 ⁇ 1
- Dimorpholino pyridazinone 0.1 xanthan gum 0.1 dicarboxylic acid polymer 0.1 acrylic acid'alkyl methacrylate copolymer ( ⁇ Murylene TR—
- Roxypoxybul polymer 0.1 sodium acrylate / 2-acrylamide-2-methylpropanesulfo Acidic acid copolymer (trade name: SIMULGEL EG, SEPPIC) 0.1
- Titanium 1.0 (Talcum coated with titanium oxide, aluminum oxide, and silicic anhydride, trade name: Riki Perleaf AR-80, Catalyst Chemical Industry Co., Ltd.) Mica Titanium 1.0 )
- Macadamia nut oil 0.1 Sorbitan sesquisoystearate 10 0 Alkyl-modified silicon resin-coated iron oxide yellow oxide 2 0 Alkyl-modified silicon resin-coated red iron oxide 0 Alkyl-modified silicon resin-coated black iron oxide 0 5 Iron oxide yellow-coated mica titanium 5.0 Synthetic phlogopite 50 Titanium oxide 1.0 Zinc oxide 1.0 Low-temperature calcined zinc oxide 4.0 Calcined sericite 1 0.0
- Talc residue (Talcum coated with titanium oxide, aluminum oxide, and silicic anhydride, trade name: Riki Parrif AR _80, Catalyst Chemicals Co., Ltd.) Talc residue
- ⁇ -refrigeration oligomer 10.0 mass 0 /.
- Cetinol 2-ethynolehexanoate 5.0 Polyoxyethylene glyceryl monostearate 1.0 Self-emulsifying glyceryl monostearate 1.0 Titanium oxide 4.0 titanium oxide 4.0 titanium oxide mica titanium oxide 5 Kaolin 3.0 Synthetic phlogopite 0.1 Cross-linked silicone powder 0.1 Silicic anhydride 5.0 Hydroxium power 0.2 Triethanolamine 0.8 Acetate DL- ⁇ -Tocopherol 0. 1 Sodium hyaluronate 0.1 Biodyne EMPP 0.1
- Ethanol 10.0 Isostearic acid 0.5 Myristic acid-treated zinc oxide 0.5 Titanium oxide coated with dextrin palmitate 1.0 0.0 Talcum coated with dextrin palmitate 7.0 Titanium oxide treated with silicone surface (30 nm) 5.0 Cross-linked silicone powder 1.0 Spherical caiiic anhydride 2.0 L-ascorbyl magnesium phosphate 0.2 Acetic acid DL- ⁇ -Tocopherol 0.1
- 1,3-butylene glycol 5.0 xylite 0.5 isostearic acid 0.5 alkyl-modified silicon resin-coated cyanic anhydride 2.0 talc 0.5 aluminum stearate 1.0 mica titanium coated with bengara 0.1 Sodium hexamethacrylate 0.05 Dicalium glycyrrhizinate 0.1
- the anti-aging agent and the collagen production promoter of the present invention are excellent in promoting collagen production and are safe. Therefore, according to the collagen production promoter and the collagen production promotion method of the present invention, it is possible to promote the production of collagen, maintain the amount of collagen, promote collagen gel contraction, and promote fibroblasts and epidermis. It promotes cell integrin production and is effective in preventing and improving wrinkles and sagging.
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Abstract
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Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/588,780 US20070134265A1 (en) | 2004-03-11 | 2004-05-18 | Anti-aging composition and collagen production promoting composition |
JP2005502978A JPWO2004075621A1 (ja) | 2004-03-11 | 2004-05-18 | 抗老化剤およびコラーゲン産生促進剤 |
EP04733645A EP1514537A4 (en) | 2004-03-11 | 2004-05-18 | AGGREGATE AGAINST THE AGING PROCESS AND PROMOTER OF COLLAGEN PRODUCTION |
US12/320,088 US20090136540A1 (en) | 2004-03-11 | 2009-01-16 | Anti-aging composition and collagen production promoting composition |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004068413 | 2004-03-11 | ||
JP2004-068413 | 2004-03-11 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/320,088 Division US20090136540A1 (en) | 2004-03-11 | 2009-01-16 | Anti-aging composition and collagen production promoting composition |
Publications (3)
Publication Number | Publication Date |
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WO2004075621A2 true WO2004075621A2 (ja) | 2004-09-10 |
WO2004075621A1 WO2004075621A1 (ja) | 2004-09-10 |
WO2004075621A3 WO2004075621A3 (ja) | 2004-12-09 |
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Cited By (22)
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JP2006117534A (ja) * | 2004-10-19 | 2006-05-11 | Kose Corp | 乳化化粧料 |
EP1661602A2 (de) * | 2004-11-26 | 2006-05-31 | Henkel Kommanditgesellschaft auf Aktien | Öl-in-wasser Emulsionen |
EP1661601A3 (de) * | 2004-11-26 | 2006-06-14 | Henkel Kommanditgesellschaft auf Aktien | Öl-in-Wasser-Emulsionen |
EP1674076A3 (fr) * | 2004-12-21 | 2006-07-12 | L'oreal | Composition cosmétique pour le maquillage résistante à l'eau et facilement démaquillable |
JP2006348017A (ja) * | 2005-05-17 | 2006-12-28 | Shiseido Co Ltd | 美容方法 |
JP2007277141A (ja) * | 2006-04-05 | 2007-10-25 | Kao Corp | 皮膚外用剤 |
JP2008520549A (ja) * | 2004-10-13 | 2008-06-19 | アーチ パーソナル ケア プロダクツ、エル.ピー. | オゾンストレス付与酵母溶解物を含有するパーソナルケア用組成物 |
JP2009040738A (ja) * | 2007-08-10 | 2009-02-26 | Pola Chem Ind Inc | 油中水乳化剤形の皮膚外用剤 |
JP2009073777A (ja) * | 2007-09-21 | 2009-04-09 | Kao Corp | 化粧料 |
WO2009084742A2 (ja) | 2009-03-30 | 2009-07-09 | Shiseido Company, Ltd. | 線維芽細胞増殖剤 |
WO2009145344A1 (ja) * | 2008-05-30 | 2009-12-03 | 株式会社 資生堂 | 水中油型皮膚外用剤 |
JP2011514320A (ja) * | 2008-02-12 | 2011-05-06 | ルサフル、エ、コンパニ | 美容用又は治療用組成物中の天然有効成分の使用 |
WO2012017555A1 (ja) * | 2010-08-06 | 2012-02-09 | 株式会社資生堂 | エラスターゼ阻害剤 |
JP2012140385A (ja) * | 2011-01-06 | 2012-07-26 | Nikko Chemical Co Ltd | 水中油型乳化化粧料 |
JP2014530887A (ja) * | 2011-10-28 | 2014-11-20 | ユニリーバー・ナームローゼ・ベンノートシヤープ | 水性光防護パーソナルケア組成物 |
JP2015510924A (ja) * | 2012-03-19 | 2015-04-13 | アイエスピー インヴェストメンツ アイエヌシー. | 大豆及び酵母のペプチド抽出物の組み合わせから成る相乗的trf2タンパク質活性化システムを含む化粧品組成物及びその使用 |
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Cited By (39)
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JP2013224328A (ja) * | 2004-10-13 | 2013-10-31 | Arch Personal Care Products Lp | オゾンストレス付与酵母溶解物を含有するパーソナルケア用組成物 |
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JP2012140385A (ja) * | 2011-01-06 | 2012-07-26 | Nikko Chemical Co Ltd | 水中油型乳化化粧料 |
JP2014530887A (ja) * | 2011-10-28 | 2014-11-20 | ユニリーバー・ナームローゼ・ベンノートシヤープ | 水性光防護パーソナルケア組成物 |
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JP2016510016A (ja) * | 2013-02-28 | 2016-04-04 | エルブイエムエイチ レシェルシェ | 褐藻抽出物、酵母抽出物及びアスコルビン酸を含有する化粧品組成物 |
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JP2018131405A (ja) * | 2017-02-15 | 2018-08-23 | 株式会社ファンケル | カリクレイン7産生促進用組成物 |
WO2019098302A1 (ja) * | 2017-11-17 | 2019-05-23 | 株式会社資生堂 | VE-カドヘリン発現促進剤及び/又はインテグリンα5発現促進剤 |
JPWO2019098302A1 (ja) * | 2017-11-17 | 2020-11-19 | 株式会社 資生堂 | VE−カドヘリン発現促進剤及び/又はインテグリンα5発現促進剤 |
US11311585B2 (en) | 2017-11-17 | 2022-04-26 | Shiseido Company, Ltd. | VE-cadherin expression promoting agent and/or integrin α5 expression promoting agent |
JP2020019743A (ja) * | 2018-08-01 | 2020-02-06 | 株式会社 資生堂 | 水中油型乳化化粧料 |
Also Published As
Publication number | Publication date |
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CN1921823A (zh) | 2007-02-28 |
WO2004075621A3 (ja) | 2004-12-09 |
TW200529879A (en) | 2005-09-16 |
EP1514537A2 (en) | 2005-03-16 |
US20070134265A1 (en) | 2007-06-14 |
JPWO2004075621A1 (ja) | 2007-08-23 |
KR20070006772A (ko) | 2007-01-11 |
US20090136540A1 (en) | 2009-05-28 |
EP1514537A4 (en) | 2012-10-31 |
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