WO2005067918A1 - 天然物由来の活性酸素消去剤およびその用途 - Google Patents
天然物由来の活性酸素消去剤およびその用途 Download PDFInfo
- Publication number
- WO2005067918A1 WO2005067918A1 PCT/JP2004/019773 JP2004019773W WO2005067918A1 WO 2005067918 A1 WO2005067918 A1 WO 2005067918A1 JP 2004019773 W JP2004019773 W JP 2004019773W WO 2005067918 A1 WO2005067918 A1 WO 2005067918A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- active oxygen
- oxygen scavenger
- acid
- fatty acid
- acid ester
- 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
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, 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
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/06—Free radical scavengers or antioxidants
Definitions
- the present invention relates to a natural product-derived active oxygen scavenger and use thereof. Furthermore, the present invention includes natural oxygen-derived active oxygen scavengers useful for foods, cosmetics, and the like, which contain flavonoids such as hydroxycaine acid derivatives as active ingredients. The present invention relates to foods and cosmetics containing an oxygen scavenger.
- Oxygen is an indispensable substance for the maintenance of life, such as the production of energy by metabolism for the living body, but it becomes reactive by various reaction systems inside and outside the living body, that is, by some immune reactions and ultraviolet irradiation. It produces abundant reactive oxygen species (superoxide aeon: ⁇ 2 ⁇ , hydrogen peroxide: H 2 0 2 , hydroxyl radical: OH ⁇ , singlet oxygen: etc.) and free radicals. These reactive oxygen species and free radicals, for example, can be used to inactivate foreign substances such as invading bacteria in certain immune reactions, but react with biological components to peroxidize lipids, proteins and nucleic acids. It is known to cause various diseases and promote aging.
- the skin is the outermost layer of the body, it is easily affected by reactive oxygen species and free radicals generated by external factors such as ultraviolet rays and radiation. It is known that the production of lipid peroxides is enhanced by abnormal skin pigmentation such as spots and buckwheat.
- the surrounding environment changes in the living body, such as infection by bacteria and viruses, changes in food intake and nutrition, excessive irradiation of ultraviolet rays, various stresses from the surroundings, aging and aging If the balance of the above network is disrupted due to, etc., the metabolic balance of active oxygen and free radicals produced in the body is disrupted, resulting in an increase in the amount of lipid peroxide, dermatitis, spots, blemishes, eczema, buckwheat, etc. It is known that various symptoms appearing as cosmetic disorders appear, and diseases such as rheumatoid arthritis, arteriosclerosis, diabetes, hepatitis, nephritis and cancer are caused.
- antioxidants added to cosmetics, foods, food additives and feeds include synthetic antioxidants such as diptylhydroxytoluene (BHT), pitylhydroxyanisole (BHA), and ethoxyquin.
- synthetic antioxidants such as diptylhydroxytoluene (BHT), pitylhydroxyanisole (BHA), and ethoxyquin.
- natural antioxidants such as ascorbic acid and vitamin E.
- the above synthetic antioxidants have excellent antioxidant effects, but some have problems with safety such as carcinogenicity, and some of them are restricted in their use.
- the above-mentioned naturally-occurring antioxidants are evaluated for safety, they have the disadvantage that their antioxidant effect is considerably inferior to that of synthetic antioxidants.
- active oxygen scavengers and removers consisting of clove oil or its component dehydrodioigenol (for example, JP-A-3-2 2 7 9 38), active oxygen scavengers containing walnut meal extract as an active ingredient (for example, see JP-A-7-69 9 12) Yes.
- propolis is known as a natural antibacterial substance and health promoting substance. This propolis is a dark-green to brown-brown sticky substance that bees make to preserve their nests. Gumy sap collected from trees by honeybees. ⁇ Plant pigment-based substances. ⁇ Made with a mixture of honey, etc.
- various biological activities such as antitumor activity, antioxidant activity, anti-inflammatory activity, and antibacterial activity have been reported.
- the group of compounds with biological activity includes cinnamate derivatives, flavonoids, esters, and other phenolic compound groups.
- the presence of terpenes was reported in subtropical propolis. Yes.
- An object of the present invention is to provide a natural product-derived active oxygen scavenger having high ability to scavenge active oxygen and free radicals and being safe for the human body, and useful for various uses, and its use. It is.
- the present inventors have obtained, for example, flavonoids, hydroxykelate derivatives, other phenolic compounds, etc. that can be obtained by extraction processing of propolis bulk powder. It was found that the object can be achieved by a substance derived from a natural product containing a plurality of kinds of active ingredients, and the present invention has been completed based on this finding.
- the above emulsifier is at least one selected from glycerin fatty acid ester, polyglycerin fatty acid ester, propylene glycol fatty acid ester, sorbitan fatty acid ester, sucrose fatty acid ester, lecithins and sapoyuns ( 1) the active oxygen scavenger derived from natural products according to (2) or (3),
- an active oxygen scavenger having high free radical scavenging ability, safe for a human body, useful for various uses, and the active oxygen scavenger are provided.
- Foods and cosmetics can be provided.
- Figure 1 is a high-speed liquid chromatogram of an example of a propolis bulk extract obtained using water as the extraction solvent.
- Figure 2 is a high-speed liquid kumatogram of an example of propolis bulk extract obtained using glycerin as the extraction solvent.
- Figure 3 is a high-performance liquid chromatogram of an example of propolis bulk extract obtained using a mixture of water and glycerin as the extraction solvent.
- Fig. 4 is a high-performance liquid chromatogram of an example of an open-police bulk extract obtained using a mixture of water, glycerin, and a disturbing agent as the extraction solvent.
- the active oxygen scavenger of the present invention contains water, an organic solvent, and an emulsifier, and has the following structure: p-coumaric acid, 3, 4 G-O-Caffeoinorequinic acid (3,4-di-Oc affeoylquinicacid), 3,5-Di-O-force ueoylquinic acid (3-, 5-di-0-caffeoyl quinicic acid), 4-Hydroxy 3-Pre-recay Cinnaic acid (4—hy dro xy—3—pre ny 1 ci nn am icacid) 3,5,7-trihydroxy-4′-methoxyflavonol (3,5,7-trihy dro xy—4 1 It is derived from natural products that contain methoxyf 1 avono 1) as a major component.
- the active oxygen scavenger of the present invention further comprises, as an active ingredient, 3, 5-diprenyl-4-hydroxyxycinnamic acid (artepiline C) [3,5-dipre ny l—4—hy dro xy ci nn am icacid (arte ⁇ 1 1 i nC)], kaem feride (kae mp heride), Belle Tonole
- Baerin Kaemferide is 4'-methoxy-3,5,7-trihydroxyflavone
- Belletol is 4,5,6-dimethyoxy 3,5,7-trihydroxyflavone
- Enorleman is 3,4'-dimethoxy- 5, 7-dihydroxy flavonol down
- chrysin 5, 7-dihydroxy flavone
- Kaemufueroru is 3, 4 5, 5, is that the 7-tetrahydroxy flavone.
- the organic solvent contained in the active oxygen scavenger of the present invention includes two or more hydroxyl groups in the molecule.
- Polyhydric alcohol compounds having the above are preferred.
- examples of the emulsifier include glycerin fatty acid ester, polyglycerin fatty acid ester, propylene glycol fatty acid ester, sorbitan fatty acid ester, sucrose fatty acid ester, and lecithin opi saponins.
- lecithins examples include soy lecithin and other plant lecithins, and examples of saponins include quilla extract and soy saponin.
- One type of these babies may be included, or two or more types may be included.
- the said babies agent can be used for foodstuffs, when using the said active oxygen scavenger for foodstuffs, it may be contained.
- the content ratio of water, the organic solvent, and the emulsifier is usually water: 5 to 50% by mass, and the organic solvent: 4 5-9 4.9 mass 0/0 and emulsifier: 0. 1 to a 1 0 mass 0/0, rather preferably is water: 5-3 0% by weight, organic solvent: 6 5-9 4. 5% by weight and emulsifier: in the range of 0.1-5% by weight.
- the total content of the active ingredients is appropriately selected according to the use of the active oxygen scavenger and is usually about 3 to 40% by mass.
- the active oxygen scavenger of the present invention can be produced, for example, by extracting and processing the propolis bulk as shown below.
- the raw propolis ingot is preferably stored at a temperature of 15 ° C or less, preferably about 0 to 10 ° C, in order to efficiently carry out the powdering and extraction process.
- the above propolis bulk is pulverized with powder S.
- the hole diameter of the screen to be attached to the powder is usually 1 to 5 mm, preferably 2 to 3 mm.
- an extraction solvent composed of a mixed solution containing water, the organic solvent, and the emulsifier in the above proportions is added to 1 part by mass of the pulverized propolis mass.
- the amount of the extraction solvent used is less than 3 parts by mass, the viscosity of the pulverized propolis mass and the extraction solvent will cause the extraction work efficiency to decrease, and if it exceeds 7 parts by mass, the effective component content may decrease. There is.
- the heat treatment is carried out at a temperature of about 50 to 90 ° C., preferably 65 to 80 ° C., and extraction is performed for about 30 to 12 ° minutes.
- the active oxygen scavenger of the present invention is obtained by removing the solid content by filtration.
- the active oxygen scavenger of the present invention thus obtained can be adjusted in concentration by distilling or adding the extraction solvent so that the concentration is suitable for the intended use. Further, if necessary, freeze-drying or spray-drying may be performed and used in powder form.
- the active oxygen scavenger of the present invention contains a wide range of components from hydrophilic to hydrophobic, such as flavonoids, hydroxycacin acid derivatives, and other phenolic compounds. In addition, it can be used for, for example, food use, chemical IS charge use, and feed use.
- the active oxygen scavenger of the present invention is an active oxygen scavenging effect obtained by blending the active ingredient as a liquid product as it is into a composition such as foods or cosmetics, or by previously formulating the active ingredient. Further, it is possible to increase the commercial value of the composition by imparting an antioxidant effect.
- Examples of pharmaceutical preparations include tablets, capsules, powders, or granules.
- the active ingredients are starches, excipients such as lactose and maetol, binders such as carboxymethylcellulose and hydroxypropylcellulose, crystalline cellulose. It can be formulated by formulating an appropriate combination of a disintegrating agent such as carboxymethyl senorelose calcium, a lubricant such as talc magnesium stearate, and other appropriate wetting agents, coloring agents and fragrances. .
- the solution may be aqueous or oily emulsion IJ or syrup, simple syrup, sorbitol, methylcellulose And suspending agents such as sodium carboxymethylcellulose, egg yolk lecithin, sorbitan monofatty acid ester, emulsifiers such as lauromacrogol and castor oil, and other preservatives, preservatives and stabilizers as needed. Can be formulated.
- An emulsifier such as amamine can be appropriately blended to prepare a preparation.
- the present invention also provides foods and cosmetics containing the active oxygen scavenger.
- the form of the food include the active oxygen scavenger itself, or seasonings such as miso, soy sauce and mayonnaise, cooking oil such as salad oil, various cooked foods, desserts, ice confectionery, persimmons, chewing gum and fruit juice, etc. A drink etc. can be mentioned.
- These foods can be used with any ingredient according to the purpose of use. For example, in the case of ice confectionery beverages, fruit juices, sweeteners, acidulants, coloring agents, flavors and the like can be appropriately blended. The amount of this active ingredient added to the food may be appropriately changed depending on the form.
- cosmetics such as lotions, emulsions, creams, facial cleansing products, packs, makeup cosmetics, cosmetics for the head, lip cosmetics, and nail products.
- cosmetics bath preparations and antiperspirants.
- arbitrary ingredients can be used according to the purpose of use.
- spherical bases such as petrolatum, paraffin, squalane, lanolin, propylene glycol, 1,3-butane.
- hydrophilic bases such as diols
- emulsifiers such as fatty acid monoglycerides, sorbitan fatty acid esters, preservatives, pigments, fragrances, and other nutrients, humectants, whitening agents, and UV absorbers as necessary.
- hydrophilic bases such as diols
- emulsifiers such as fatty acid monoglycerides, sorbitan fatty acid esters, preservatives, pigments, fragrances, and other nutrients, humectants, whitening agents, and UV absorbers
- the necessary components according to the type can be appropriately blended. What is necessary is just to change suitably the addition amount to the cosmetics of the active ingredient of this invention according to the form.
- the active oxygen scavenger of this invention can also be mix
- feeds can be mentioned, for example, livestock, poultry, fish powders, kneaded products or pellets.
- Any component can be used depending on the purpose of use.
- coloring agents, flavors, and the like can be appropriately blended.
- the amount of force applied to the feed of the active ingredient of the present invention may be appropriately changed depending on the form. '
- propolis food standard component content was measured by the Japan Health and Nutrition Food Association Propolis Food Standard Component Content Measurement Method (revised in 2001). The results are shown in Table 1.
- the propolis bulk extract (d) (active oxygen scavenger of the present invention) obtained using an extraction solvent (d) consisting of a mixture of water, an organic solvent and an emulsifier is a propolis food standard.
- Ingredient content (Quercetin equivalent, mass%) Force Propolis bulk extract obtained using other extraction solvents (a), (b), (c) (a), (b),
- propolis bulk extract (d) exhibits a high D P P H radical scavenging activity almost as high as the propolis bulk extracts (b) and (c).
- the propolis bulk mass extracts (a), (b), (c), and (d) obtained in (1) above were analyzed by high performance liquid chromatography (HP LC).
- Propolis bulk extract (a), (b), (c), (d) is dissolved in distilled water for HPLC (Wako Pure Chemical Industries) or methanol for HP LC (concentration: l OmgZml), Nezarts (0. 45 ⁇ , Go ettingen, Germa After filtration at ny), 10/1 was used for HPLC analysis.
- the peak areas and peak heights of the hydrophilic compounds a to h are almost the same in the four types of propolis bulk extracts, and the dominant tendency in the propolis bulk extract (d) is confirmed. It is.
- propolis is excluded except for compounds m, o (3, 5, 7-trihydroxy-4, -methoxyflavonol) and z (3,5-diprenyl-4-hydroxyoxycinnamic acid).
- m 3, 5, 7-trihydroxy-4, -methoxyflavonol
- z 3,5-diprenyl-4-hydroxyoxycinnamic acid
- the active oxygen scavenger of the present invention is highly safe for the human body and has a high active oxygen 'free radical scavenging ability and antioxidation ability, and is suitably used for foods, cosmetics, feeds, etc. It is done.
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- Coloring Foods And Improving Nutritive Qualities (AREA)
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Abstract
Description
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Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BRPI0409330-5A BRPI0409330A (pt) | 2004-01-16 | 2004-12-24 | eliminador de oxigênio ativo derivado de substáncia natural e seu uso |
US10/550,602 US20060110520A1 (en) | 2004-01-16 | 2004-12-24 | Active oxygen eliminator derived from natural substance and use thereof |
EP04808123A EP1621194A4 (en) | 2004-01-16 | 2004-12-24 | ACTIVE OXYGEN ELIMINATOR OF NATURAL MATERIAL AND ITS USE |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004-8862 | 2004-01-16 | ||
JP2004008862A JP2005200360A (ja) | 2004-01-16 | 2004-01-16 | 天然物由来の活性酸素消去剤およびその用途 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2005067918A1 true WO2005067918A1 (ja) | 2005-07-28 |
Family
ID=34792249
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2004/019773 WO2005067918A1 (ja) | 2004-01-16 | 2004-12-24 | 天然物由来の活性酸素消去剤およびその用途 |
Country Status (6)
Country | Link |
---|---|
US (1) | US20060110520A1 (ja) |
EP (1) | EP1621194A4 (ja) |
JP (1) | JP2005200360A (ja) |
BR (1) | BRPI0409330A (ja) |
TW (1) | TW200528124A (ja) |
WO (1) | WO2005067918A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110179750A (zh) * | 2019-06-17 | 2019-08-30 | 四川九章生物科技有限公司 | 一种绿原酸自乳化组合物及其用途 |
CN117442600A (zh) * | 2023-09-27 | 2024-01-26 | 深圳昱朋科技有限公司 | 一种雾化香精添加剂、雾化香精及气溶胶生成装置 |
Families Citing this family (10)
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---|---|---|---|---|
US7556750B2 (en) | 2005-04-08 | 2009-07-07 | Transitions Optical, Inc. | Photochromic materials with reactive substituents |
US8647538B2 (en) | 2005-04-08 | 2014-02-11 | Transitions Optical, Inc. | Photochromic compounds having at least two photochromic moieties |
US20060228557A1 (en) * | 2005-04-08 | 2006-10-12 | Beon-Kyu Kim | Photochromic materials having extended pi-conjugated systems and compositions and articles including the same |
US9139552B2 (en) | 2005-04-08 | 2015-09-22 | Transitions Optical, Inc. | Indeno-fused naphthopyrans having ethylenically unsaturated groups |
US9028728B2 (en) | 2005-04-08 | 2015-05-12 | Transitions Optical, Inc. | Photochromic materials that include indeno-fused naphthopyrans |
EP2055196A1 (en) * | 2007-10-29 | 2009-05-06 | Givaudan SA | Sweet flavour modulating carboxyalkyl-substituted phenyl derivatives |
FR2928543B1 (fr) * | 2008-03-17 | 2013-08-02 | Oreal | Utilisation d'inhibiteurs de la xanthine oxydase pour la pigmentation capillaire |
CN101587065B (zh) * | 2009-06-25 | 2011-11-30 | 上海理工大学 | 等离子体功能化碳纳米管表面氧自由基的检测方法 |
MX370090B (es) | 2013-02-01 | 2019-10-25 | Centro De Investig En Alimentacion Y Desarrollo A C | Un método y un sistema para el tratamiento integral de aguas residuales de una industria del maíz. |
JP2014237604A (ja) * | 2013-06-06 | 2014-12-18 | 株式会社創研 | 皮脂分泌抑制剤及びこれを含有する外用組成物 |
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2004
- 2004-01-16 JP JP2004008862A patent/JP2005200360A/ja active Pending
- 2004-12-24 EP EP04808123A patent/EP1621194A4/en not_active Withdrawn
- 2004-12-24 BR BRPI0409330-5A patent/BRPI0409330A/pt not_active IP Right Cessation
- 2004-12-24 WO PCT/JP2004/019773 patent/WO2005067918A1/ja not_active Application Discontinuation
- 2004-12-24 US US10/550,602 patent/US20060110520A1/en not_active Abandoned
-
2005
- 2005-01-13 TW TW094101032A patent/TW200528124A/zh unknown
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See also references of EP1621194A4 * |
TAZAWA S. ET AL.: "Mitsubashi Yurai Genryo Sono Genjo to Oyo to Jissai Propolis no Seibun Bunseki to kagakuteki Hinshitsu Oyobi Tyrosinase Sogai Kassei.", FRAGRANCE JOURNAL., vol. 30, no. 3, 2002, pages 25 - 32, XP002990241 * |
TSUTSUMI T. ET AL.: "Mitsubachi yurai genryo sono genjo to oyo to jissai mitsubashi yurai genryo no koshohin eno oyo.", FRAGRANCE JOURNAL., vol. 30, no. 3, 2002, pages 17 - 24, XP002963464 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN110179750A (zh) * | 2019-06-17 | 2019-08-30 | 四川九章生物科技有限公司 | 一种绿原酸自乳化组合物及其用途 |
CN117442600A (zh) * | 2023-09-27 | 2024-01-26 | 深圳昱朋科技有限公司 | 一种雾化香精添加剂、雾化香精及气溶胶生成装置 |
Also Published As
Publication number | Publication date |
---|---|
EP1621194A4 (en) | 2007-01-10 |
BRPI0409330A (pt) | 2006-04-25 |
US20060110520A1 (en) | 2006-05-25 |
EP1621194A1 (en) | 2006-02-01 |
TW200528124A (en) | 2005-09-01 |
JP2005200360A (ja) | 2005-07-28 |
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