WO2015011750A1 - Moisturizing agent - Google Patents

Moisturizing agent Download PDF

Info

Publication number
WO2015011750A1
WO2015011750A1 PCT/JP2013/069747 JP2013069747W WO2015011750A1 WO 2015011750 A1 WO2015011750 A1 WO 2015011750A1 JP 2013069747 W JP2013069747 W JP 2013069747W WO 2015011750 A1 WO2015011750 A1 WO 2015011750A1
Authority
WO
WIPO (PCT)
Prior art keywords
sugar
component
polyhydric alcohol
kluyveromyces
mass
Prior art date
Application number
PCT/JP2013/069747
Other languages
French (fr)
Japanese (ja)
Inventor
豊明 小林
上原 静香
Original Assignee
株式会社コーセー
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 株式会社コーセー filed Critical 株式会社コーセー
Priority to PCT/JP2013/069747 priority Critical patent/WO2015011750A1/en
Priority to CN201480032571.1A priority patent/CN105263471B/en
Priority to JP2015528256A priority patent/JP6382815B2/en
Priority to PCT/JP2014/069088 priority patent/WO2015012198A1/en
Priority to TW103124871A priority patent/TWI636797B/en
Publication of WO2015011750A1 publication Critical patent/WO2015011750A1/en
Priority to HK16101803.7A priority patent/HK1213786A1/en

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • 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
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/345Alcohols containing more than one hydroxy group
    • 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
    • A61K8/9728Fungi, e.g. yeasts
    • 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]
    • A61K8/9794Liliopsida [monocotyledons]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/85Products or compounds obtained by fermentation, e.g. yoghurt, beer, wine
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q7/00Preparations for affecting hair growth

Definitions

  • the present invention relates to a humectant.
  • Moisturizing ingredients are blended in topical skin preparations, cosmetics, quasi-drugs, and the like for the purpose of adjusting moisture on the skin surface to give moist and moist feeling to the skin and hair.
  • the skin barrier function tends to decrease.
  • skin troubles such as dry skin, wrinkles, and rough skin are likely to occur, and improvement of skin inflammation is delayed. For this reason, increasing and retaining the moisture in the stratum corneum has been expected to be used for various purposes because it leads to keeping the skin soft, elastic and protecting the dermis.
  • a moisturizing component for example, glycerin having high hygroscopicity has been used.
  • these components are easily affected by the surrounding humidity, and do not exhibit a sufficient effect on dry skin, but also have the problem of taking away moisture from the skin and promoting drying. For this reason, at present, attention is focused mainly on biological component-derived or biologically similar components.
  • NMF NATURAL MOISTURIZING FACTOR
  • amino acids eg, glycine, ⁇ -alanine, etc.
  • high molecular compounds such as hyaluronic acid, soluble collagen, ceramide, etc.
  • Patent Document 1 proposes a humectant containing lysyl- ⁇ -alanine or a salt thereof.
  • the present invention is intended to provide an excellent moisturizing agent in view of such circumstances.
  • the present inventor has (A) a sugar fermented product obtained from yeast belonging to the genus Kluyveromyces, and (B) a specific gravity at 20 ° C. of 0.93 or more. It has been found that an excellent moisturizing effect can be obtained by using together with a monohydric alcohol, and the present invention has been completed.
  • the present invention provides the following components (A) and (B): (A) Sugar fermented product from yeast of the genus Kluyveromyces (B) A humectant containing a polyhydric alcohol having a specific gravity at 20 ° C. of 0.93 or more is provided.
  • the polyhydric alcohol of component (B) may be a polyhydric alcohol having a specific gravity at 20 ° C. of 1.01 or more.
  • the polyhydric alcohol of component (B) may be one or more selected from glycerin, propanediol, propylene glycol, and dipropylene glycol.
  • an excellent moisturizing agent can be provided.
  • the moisturizing agent of the present disclosure contains, as active ingredients, component (A) a sugar fermented product of Kluyveromyces yeast and component (B) a polyhydric alcohol having a specific gravity at 20 ° C. of 0.93 or more. Is.
  • component (A) sugar fermented product of yeast of the genus Kluyveromyces (hereinafter also referred to as “component (A) sugar fermented product”) used in the present disclosure will be described.
  • the “Kluyveromyces yeast” used in the present disclosure is not particularly limited, and one or more of the following exemplified yeast species can be selected and used.
  • yeast examples include, for example, Kluyveromyces thermotolerans, Kluyveromyces africanus, Kluyveromyces fragilis, Kluyveromyces lactis, Kluyveromyces phaffii, Kluyveromyces waltii, Kluyveromyces wickerhamii, Kluyveromyces wickerhamii, Kluyveromyces warrowhamii Is mentioned.
  • Kluyveromyces thermotolerans Kluyveromyces thermotolerans
  • Kluyveromyces lactis Kluyveromyces lactis
  • Kluyveromyces fragilis more preferably Kluyveromyces fragilis.
  • Tolerance Keluyveromyces thermotolerans
  • These yeasts have long been used for producing dairy products such as cheese and yogurt, wine, and fermented foods such as pickles.
  • Kluyveromyces thermotolerance has been reported as a lactic acid-producing yeast isolated from wine brewing and plum jam fermentation products along with its biochemical and physiological properties (Reference 1: The Yeasts.A). Taxonomic Study, 4th ed. Elsevier Science BV, Amsterdam. 240-241 (1998)).
  • Kluyveromyces thermotolerans examples include Kluyveromyces thermotolerans MA KT (NITE BP-1420).
  • the Kluyveromyces genus yeast used in the present disclosure is an extremely safe microorganism for the human body and can also eat sugar as a fermentation raw material. Therefore, the component (A) sugar of the present disclosure Fermented products are considered to be highly safe.
  • the “sugar” used as a raw material for the component (A) fermented sugar of the present disclosure is not particularly limited, and those containing sucrose are preferable.
  • the “sugar” may be in any form such as powder or liquid.
  • sugar derived from sugarcane is preferable, and sugarcane sugar obtained from sugarcane squeezed juice is more preferable.
  • sugars derived from sugarcane include unpurified sugars such as Wasanbon, molasses, black honey, honey-containing sugar, crude sugar, brown sugar, and the like; and refined sugars such as upper white sugar and granulated sugar. More than one species can be selected.
  • unpurified sugar that has not been purified to upper white sugar is preferred, and among the unpurified sugars, brown sugar is preferred.
  • Brown sugar is produced by heating and concentrating sugarcane squeezed juice, and is preferably not subjected to separation and purification of sugar.
  • the “sugarcane” of the present disclosure is a plant belonging to the genus Sugarcane (sugar cane, scientific name: Saccharum officinarum), and is also called sweet potato.
  • the component (A) sugar fermented product of the present disclosure is preferably a fermented product obtained by culturing Kluyveromyces yeast in a sugar-containing medium.
  • the content of sugar in the sugar-containing medium of the present disclosure is not particularly limited, but is preferably 3 to 15% by mass, more preferably 4 to 8% by mass.
  • the sugar-containing medium of the present disclosure is preferably a liquid.
  • the sugar-containing liquid medium include an aqueous sugar solution obtained by mixing the above-described sugar and water. The water is not particularly limited.
  • the sugar-containing medium preferably contains medium components (for example, a carbon source, a nitrogen source, inorganic salts, etc.) usually used for yeast in terms of improving the productivity of the fermented product.
  • medium components for example, a carbon source, a nitrogen source, inorganic salts, etc.
  • the culture method of the Kluyveromyces genus yeast is not particularly limited as long as it is a culture method usually used for yeast, and can follow a known method (for example, see Reference 1). For example, shaking culture, aeration culture, stationary culture, stirring culture and the like can be mentioned. Moreover, any of a batch type and a continuous type may be sufficient. These can be performed alone or in combination of two or more.
  • the culture conditions (for example, aerobic, anaerobic, pH in the medium, dissolved oxygen, culture temperature, culture time, etc.) of the Kluyveromyces yeast are not particularly limited, and can be appropriately selected according to the purpose. it can.
  • the component (A) fermented sugar of the present disclosure is preferably prepared by aerobic culture in a sugar-containing medium inoculated with pre-cultured Kluyveromyces yeasts. At this time, it is preferable to add 1% of the preculture solution to the sugar-containing medium. At this time, it is preferable to perform the aerobic culture at a medium pH of 5 to 7 at 15 to 35 ° C. for 1 to 3 days. As the preferred culture, it is desirable to perform shaking culture or stirring culture under aerobic conditions. In the case of aerobic conditions, air (about 20% by volume of oxygen) treated with a sterilization filter may be used.
  • the preparation of the present disclosure does not actively perform ethanol fermentation as in alcoholic beverage production, but the ethanol concentration in the sugar fermentation product after the preparation is less than 1% by mass (preferably 0.1% by mass or less) ) Is preferable in terms of the moisturizing effect.
  • the component (A) sugar fermented product of the present disclosure can be used as it is or after it is dried.
  • cells of Kluyveromyces genus yeast may be removed by a conventional method such as centrifugation or membrane treatment.
  • the component (A) fermented sugar product of the present disclosure may be a diluted solution, a concentrated solution, or a dried product, and may be a separated product or a purified product according to the purpose.
  • a physiological saline solution may be used, and when drying, a freeze drying method or a spray drying method may be used.
  • component (B) polyhydric alcohol having a specific gravity at 20 ° C. (g / mL at 20 ° C.) of 0.93 or more” (hereinafter also referred to as “component (B) polyhydric alcohol”) used in the present disclosure will be described. .
  • the component (B) of the present disclosure can be prepared by selecting one or more of the following examples of the component (B) polyhydric alcohol.
  • Component (B) “polyhydric alcohol having a specific gravity of 0.93 or more at 20 ° C.” of the present disclosure includes methylene glycol, glycol (ethylene glycol), propylene glycol, propanediol (1,3-propanediol), diethylene glycol Coal, methylenepropanediol, 1,2-butylene glycol, 1,3-butylene glycol, 1,4-butylene glycol, 2,3-butanediol, 1,2-pentanediol, 1,3-pentanediol, 1, 4-pentanediol, 1,5-pentanediol, 2,4-pentanediol, 1,2-cyclopentanediol, 1,3-cyclopentanediol, neopentyl glycol, isopentyldiol, aminoethylpropanediol, 1, 2-hexanediol, 1,6-hex
  • the specific gravity (g / mL at 20 ° C.) of the component (B) polyhydric alcohol of the present disclosure is preferably 1.01 or more, more preferably 1.03 or more. When used together, the moisture retention can be further improved, which is preferable. Moreover, the specific gravity (g / mL at 20 ° C.) of the polyhydric alcohol of the present disclosure is preferably 2 or less.
  • the alcohol valence of the polyhydric alcohol is preferably 2 to 4, more preferably 2 to 3.
  • the component (B) polyhydric alcohol preferably has 6 or less carbon atoms, more preferably 2 to 4 carbon atoms.
  • the refractive index of the component (B) polyhydric alcohol is preferably 1.3 to 1.6, more preferably 1.4 to 1.5.
  • component (B) polyhydric alcohols propylene glycol, propanediol, 1,2-butylene glycol, 1,3-butylene glycol, 1,2-pentanediol, dipropylene glycol and glycerin are preferred. Furthermore, propylene glycol, propanediol, dipropylene glycol and glycerin are more preferable among the components (B) from the viewpoint of improving moisture retention.
  • the “specific gravity at 20 ° C.” of the polyhydric alcohol is a value measured by the specific gravity measurement method No. 1 described in the Ministry of Health, Labor and Welfare: Quasi-drug raw material standard 2006 (published by Yakuji Nipposha).
  • the “refractive index at 20 ° C.” of the polyhydric alcohol is a value measured by a refractive index measurement method described in Japan Ministry of Health, Labor and Welfare: Quasi-drug raw material standard 2006 (published by Yakuji Nippo).
  • the preparation of the humectant of the present disclosure combines the component (A) sugar fermented product and the component (B) polyhydric alcohol, and therefore, these may be mixed. When combining these, it is preferable to use a sugar fermentation liquid (preferably an aqueous solution) as the component (A) sugar fermentation product.
  • a sugar fermentation liquid preferably an aqueous solution
  • the content ratio of the component (A) sugar fermented product and the component (B) polyhydric alcohol in the moisturizing agent of the present disclosure (parts by mass of dry solids: parts by mass) is not particularly limited, but from the viewpoint of improving moisturizing properties. The ratio is preferably 0.09: 0.5 to 0.09: 30, more preferably 0.09: 1 to 0.09: 20, and still more preferably 0.09: 5 to 0.09: 10.
  • the content of the component (B) polyhydric alcohol in the moisturizing agent is preferably 1 to 30% by mass, more preferably 5 to 20% by mass. In addition, it is possible to adjust so that it may become 100 mass% of humectants using water.
  • the form of the moisturizing agent of the present disclosure to be obtained is not particularly limited, but liquid or semi-solid is preferable.
  • the moisture retention can be dramatically improved as compared with the case where each component is used alone. Admitted. Therefore, since the mixture of the component (A) and the component (B) has a very excellent moisturizing property, it may be used for moisturizing and various preparations intended for use for moisturizing. It can also be used to produce these various formulations. Moreover, since the combination of the said component (A) and the said component (B) has the outstanding moisturizing property, it is used for the method for aiming at prevention, improvement, and / or treatment of various symptoms, conditions, etc. regarding skin by moisturizing. can do.
  • the various symptoms and conditions include rough skin, wrinkle formation, skin aging, xeroderma, dandruff, and the like.
  • the combination of the said component (A) and the said component (B) can give a moist feeling to a target object (for example, skin, hair, foodstuff, etc.).
  • a target object for example, skin, hair, foodstuff, etc.
  • the combination of the said component (A) and the said component (B) can be used in order to give a moist feeling and a feeling of unity to hair, and, thereby, can suppress hairiness.
  • the component (A) sugar fermented product and the component (B) polyhydric alcohol are used in order to improve or impart moisturizing properties, such as external preparations for skin, cosmetics, quasi drugs, pharmaceuticals, foods and functional foods.
  • the moisturizing agent of the present disclosure can be the above-mentioned external preparation for skin, cosmetics, foods and the like. Moreover, you may make these preparations contain the moisturizer containing the said component (A) of this indication, and the said component (B).
  • the humectant of the present disclosure or the component (A) fermented sugar and the component (B) polyhydric alcohol are particularly suitable for use in external preparations for skin, cosmetics, quasi drugs, etc.
  • a preparation to be contacted by application or the like is preferable.
  • skin external preparations and cosmetics include skin lotions, emulsions (oil-in-water type, etc.), creams (oil-in-water type), pack cosmetics, liquid foundations, ointments, hair nourishing agents, hair protectants and the like.
  • the content of the component (A) fermented sugar in the preparation of the present disclosure is preferably 0.001 to 0.095% by mass, more preferably as a dry solid content, from the viewpoint of the stability of the preparation and moisture retention. It is 0.005 to 0.05 mass%, more preferably 0.001 to 0.02 mass%.
  • the content of the component (B) polyhydric alcohol in the preparation of the present disclosure is preferably 1 to 50% by mass, more preferably 5 to 40% by mass, and further preferably 10 to 30% from the viewpoints of safety and moisture retention. % By mass.
  • the content ratio of the component (A) sugar fermented product and the component (B) polyhydric alcohol in the formulation of the present disclosure is not particularly limited, but the stability and moisture retention of the formulation From this viewpoint, it is preferably 0.01: 5 to 0.01: 500, more preferably 0.01: 10 to 0.01: 300, and still more preferably 0.01: 20 to 0.01: 200.
  • moisturizer of the present disclosure and the preparation of the present disclosure are necessary as long as the effects of the present technology are not impaired in addition to the component (A) fermented sugar and the component (B) polyhydric alcohol of the present disclosure.
  • optional components may be used in combination.
  • components may be pharmaceutically acceptable components, such as preservatives, cell activators, antioxidants, humectants, UV inhibitors, solvents (water, alcohols, etc.), oils, interfaces Activator, Thickener, Powder, Chelating agent, pH adjuster, Emulsifier, Stabilizer, Colorant, Brightener, Flavoring agent, Flavoring agent, Excipient, Binder, Disintegrant, Lubricant, Dilution Agents, osmotic pressure adjusting agents, fragrances and the like, and these may be added according to the intended preparation.
  • the form of the preparation is not particularly limited, and may be any form such as liquid, paste, gel, solid, and powder.
  • this technique can also employ
  • humectant according to any one of [1] to [3], wherein the polyhydric alcohol of component (B) is a polyhydric alcohol having a specific gravity at 20 ° C. of 1.01 or more.
  • the polyhydric alcohol of component (B) is one or more selected from glycerin, propanediol, propylene glycol, and dipropylene glycol. The humectant described.
  • the yeast belonging to the genus Kluyveromyces is one selected from Kluyveromyces thermotolerans, Kluyveromyces lactis and Kluyveromyces fragilis
  • the component (A) fermented sugar product is a fermented product obtained by culturing Kluyveromyces yeast in a sugar (preferably unpurified sugar) -containing medium.
  • the humectant according to any one of the above.
  • ⁇ Preparation Example 1 Preparation of brown sugar fermentation broth by Kluyveromyces thermotolerans> [Pre-culture] Liquid culture of Kluyveromyces thermotolerance MA KT (NITE BP-1420) was performed using YPD medium (pH 6.0). One platinum loop of the liquid culture solution was taken and inoculated into a YM medium (solid medium), and precultured at 25 ° C. for 2 days.
  • YPD Yeast Extract-Peptone- Dextrose
  • YM Yeast Mold
  • MA KT (NITE BP-1420) is a country of origin: Japan / source: collected from sap, classified as Lachancea (Kluyveromyces) thermotolerans based on morphology and bacteriological properties, and named MA KT It is. The strain was deposited on September 13, 2012 at the depository: 2-5-8, Kazusa Kamashichi, Kisarazu City, Chiba Prefecture 292-0818, Japan, and the National Institute of Technology and Technology (NPMD). It is what.
  • Examples 1 to 7 and Comparative Examples 1 and 2 Production of moisturizing agent>
  • the brown sugar fermentation broth prepared in Preparation Example 1 was mixed so that the solid content concentration was 0.09% by mass and each polyhydric alcohol shown in Table 1 was 10% by mass, and Examples 1 to 7 and Comparative Examples 1 to 2 were mixed. A humectant was produced.
  • the sample which mixed the purified water instead of the brown sugar fermentation liquid was also prepared.
  • the specific gravity was measured by the specific gravity measurement method No. 1 described in Japan Ministry of Health, Labor and Welfare: Quasi-drug raw material standard 2006 (published by Yakuji Nippo Co., Ltd.).
  • the refractive index was measured by the refractive index measurement method described in the Ministry of Health, Labor and Welfare: quasi-drug raw material standard 2006 (published by Yakuji Nippo Co., Ltd.). No symbol: Quasi-drug raw material standard 2006 # 1 MERCK INDEX ELEVENTH EDITION # 2 Chemical Handbook Basics I (The Chemical Society of Japan, revised 4th edition) # 3 Cosmetics Handbook (Nikko Chemicals) # 4 Chemical book
  • the moisturizing effect was measured by the following method. After washing the inner part of the forearm, the measurement site (2 cm ⁇ 2 cm) was marked. It was acclimatized for 20 minutes under an air temperature of 20 ° C. and a humidity of 50%, and the moisture content was measured with Skicon200 (IBSCo. Ltd.). This value was taken as the value before coating. Thereafter, 100 ⁇ L of the sample was impregnated into a 2 cm ⁇ 2 cm tissue paper, and then placed on the measurement site and allowed to stand for 5 minutes. The tissue paper was peeled off and the sample was applied to the skin with a finger. The value obtained by measuring the moisture content with Skicon200 (IBSCo. Ltd.) 60 minutes after the completion of coating was taken as the value after 60 minutes.
  • FIGS. S is the time when the mixed solution of brown sugar fermented liquid and polyhydric alcohol is applied
  • w is the time when the mixed liquid of brown sugar fermented liquid and purified water is applied
  • the water content after 60 minutes of application is A
  • the water content before coating B As / Bs and Aw / Bw at this time are shown in FIG.
  • (As / Bs) / (Aw / Bw) is shown in FIG.
  • Comparative Example 2 in which brown sugar fermented liquid and purified water were combined, the amount of water was lower than before application, but the brown sugar fermented liquid was combined with polyhydric alcohol having a specific gravity of 0.93 or higher at 20 ° C.
  • the water content was kept high until 60 minutes after application. That is, by combining a sugar fermentation product from yeast of the genus Kluyveromyces with a polyhydric alcohol having a specific gravity of 0.93 or higher at 20 ° C., the moisture content is dramatically increased compared to the case where each is used alone. It was observed that the sex was improved. It was recognized that the moisture retention was significantly improved when the specific gravity of the polyhydric alcohol exceeded 1.0065.
  • Latex (Ingredient) (mass%) 1. Polyoxyethylene (20) sorbitan monooleate 1.0 2. Sorbitan sesquioleate 0.5 3. Glyceryl trioctanoate 0.5 4). Jojoba oil 0.5 5. Squalane 0.5 6). 6. Purified water remaining amount Edetate disodium 0.1 8). Methylparaben 0.2 9. Phenoxyethanol 0.5 10. Glycerin 5.0 11. Propanediol 1.0 12 Propylene glycol 2.0 13. Sodium lactate 0.5 14. 2-O- ⁇ -D-glucosyl-L-ascorbic acid 1.0 15. Brown sugar fermentation broth of Preparation Example 1 (solid content concentration 0.1% by mass) 20.0 16. Xanthan gum 0.05 17.
  • MA KT (NITE BP-1420) strain / Classification: Lachancea (Kluyveromyces) thermotolerans / Depositary: 292-0818, Kisarazu City, Chiba Pref. (NPMD) / Contract date: September 13, 2012.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Mycology (AREA)
  • Microbiology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Biotechnology (AREA)
  • Botany (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Toxicology (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Abstract

The purpose of the present invention is to provide an excellent moisturizing agent. This moisturizing agent includes: a sugar fermentation product (A) obtained using a yeast belonging to Kluyveromyces; and a polyhydric alcohol (B) having a specific gravity at 20˚C of at least 0.93. The polyhydric alcohol (B) may have a specific gravity at 20˚C of at least 1.01. Furthermore, the polyhydric alcohol (B) may be at least one selected from glycerin, propanediol, propylene glycol, and dipropylene glycol.

Description

保湿剤Moisturizer
 本発明は、保湿剤に関する。 The present invention relates to a humectant.
 保湿成分は、皮膚表面の水分調整をして、皮膚、毛髪等に潤いのあるしっとり感を与える目的で、皮膚外用剤、化粧料や医薬部外品等に配合されている。
 皮膚の表皮の最外層にある角質層の水分が減少し、保湿機能が低下すると皮膚バリア機能も低下しやすい。皮膚バリア機能が低下すると、例えば、乾燥肌、シワ、肌荒れ等の肌トラブルになりやすく、また皮膚炎症の改善が遅くなる。
 このため、角質層の水分を増加及び保持することは、皮膚を柔軟に保ち、弾力性を持たせ、真皮を保護することに繋がることから、色々な目的での利用が期待されてきた。このような保湿成分としては例えば吸湿性が高いグリセリンなどが用いられてきた。しかしながら、これらの成分は周りの湿度に影響されやすく、乾燥肌においては十分な効果を発揮しないばかりか、肌の水分を奪い取り乾燥を促進させると言う問題があった。
 このため、現在は、主に生体成分由来又は生体類似成分が注目されている。具体的にはNMF(NATURAL MOISTURIZING FACTOR)である乳酸ナトリウム、アミノ酸類(例えば、グリシン、β-アラニン等)やヒアルロン酸、可溶性コラーゲン等の高分子化合物、また、セラミド等が用いられている。
 例えば、特許文献1には、リシル-β-アラニン又はその塩を含有する保湿剤が提案されている。
 しかしながら、使用者は様々な保湿成分を求めているため、さらなる保湿成分の研究開発が進められている。
Moisturizing ingredients are blended in topical skin preparations, cosmetics, quasi-drugs, and the like for the purpose of adjusting moisture on the skin surface to give moist and moist feeling to the skin and hair.
When the water content of the stratum corneum in the outermost layer of the skin epidermis decreases and the moisture retention function decreases, the skin barrier function tends to decrease. When the skin barrier function is lowered, for example, skin troubles such as dry skin, wrinkles, and rough skin are likely to occur, and improvement of skin inflammation is delayed.
For this reason, increasing and retaining the moisture in the stratum corneum has been expected to be used for various purposes because it leads to keeping the skin soft, elastic and protecting the dermis. As such a moisturizing component, for example, glycerin having high hygroscopicity has been used. However, these components are easily affected by the surrounding humidity, and do not exhibit a sufficient effect on dry skin, but also have the problem of taking away moisture from the skin and promoting drying.
For this reason, at present, attention is focused mainly on biological component-derived or biologically similar components. Specifically, NMF (NATURAL MOISTURIZING FACTOR) sodium lactate, amino acids (eg, glycine, β-alanine, etc.), high molecular compounds such as hyaluronic acid, soluble collagen, ceramide, etc. are used.
For example, Patent Document 1 proposes a humectant containing lysyl-β-alanine or a salt thereof.
However, since users are seeking various moisturizing ingredients, research and development of further moisturizing ingredients is underway.
国際公開2008/126652号パンフレットInternational Publication No. 2008/1266652 Pamphlet
 よって、本発明は、斯かる実情に鑑み、優れた保湿剤を提供しようとするものである。 Therefore, the present invention is intended to provide an excellent moisturizing agent in view of such circumstances.
 そこで、本発明者は、鋭意検討した結果、安全性が高いと考えられる(A)クルイベロマイセス属の酵母による糖発酵物と、(B)20℃での比重が0.93以上の多価アルコールとを併用することによって、優れた保湿効果が得られることを見出し、本発明を完成させた。 Therefore, as a result of intensive studies, the present inventor has (A) a sugar fermented product obtained from yeast belonging to the genus Kluyveromyces, and (B) a specific gravity at 20 ° C. of 0.93 or more. It has been found that an excellent moisturizing effect can be obtained by using together with a monohydric alcohol, and the present invention has been completed.
 よって、本発明は、次の成分(A)及び(B);
(A)クルイベロマイセス属の酵母による糖発酵物
(B)20℃での比重が0.93以上の多価アルコール
を含有する保湿剤を提供するものである。
 成分(B)の多価アルコールが、20℃での比重が1.01以上の多価アルコールでもよい。
 成分(B)の多価アルコールが、グリセリン、プロパンジオール、プロピレングリコール、ジプロピレングリコールから選ばれる1種又は2種以上のものでもよい。
Thus, the present invention provides the following components (A) and (B):
(A) Sugar fermented product from yeast of the genus Kluyveromyces (B) A humectant containing a polyhydric alcohol having a specific gravity at 20 ° C. of 0.93 or more is provided.
The polyhydric alcohol of component (B) may be a polyhydric alcohol having a specific gravity at 20 ° C. of 1.01 or more.
The polyhydric alcohol of component (B) may be one or more selected from glycerin, propanediol, propylene glycol, and dipropylene glycol.
 本発明によれば、優れた保湿剤を提供することができる。 According to the present invention, an excellent moisturizing agent can be provided.
黒糖発酵液と多価アルコールの保湿効果(塗布前を1としたときの変化率)確認試験の結果を示す図である。It is a figure which shows the result of the moisturizing effect (change rate when application is set to 1) confirmation test of brown sugar fermented liquor and polyhydric alcohol. 黒糖発酵液と多価アルコールの保湿効果(黒糖発酵液の変化率/精製水の変化率)確認試験の結果を示す図である。It is a figure which shows the result of the moisturizing effect (change rate of brown sugar fermentation liquid / change rate of purified water) confirmation test of brown sugar fermentation liquid and polyhydric alcohol.
 本開示の保湿剤は、成分(A)クルイベロマイセス属の酵母による糖発酵物と、成分(B)20℃での比重が0.93以上の多価アルコールと、を有効成分として含有するものである。 The moisturizing agent of the present disclosure contains, as active ingredients, component (A) a sugar fermented product of Kluyveromyces yeast and component (B) a polyhydric alcohol having a specific gravity at 20 ° C. of 0.93 or more. Is.
 本開示に用いられる「成分(A)クルイベロマイセス属(Kluyveromyces)の酵母による糖発酵物」(以下、「成分(A)糖発酵物」ともいう)について説明する。 The “component (A) sugar fermented product of yeast of the genus Kluyveromyces” (hereinafter also referred to as “component (A) sugar fermented product”) used in the present disclosure will be described.
 本開示に用いる「クルイベロマイセス属(Kluyveromyces)の酵母」は、特に限定されず、以下の例示の酵母種を1種又は2種以上選択して使用することができる。
 前記「クルイベロマイセス属(Kluyveromyces)酵母」として、例えば、クルイベロマイセス・サーモトレランス(Kluyveromyces thermotolerans)、クルイベロミセス・アフリカヌス(Kluyveromyces africanus)、クルイベロミセス・フラジリス(Kluyveromyces fragilis)、クルイベロミセス・ラクティス(Kluyveromyces lactis)、クルイベロミセス・ファフィー(Kluyveromyces phaffii)、クルイベロミセス・ウォルティ(Kluyveromyces waltii)、クルイベロミセス・ウィッカーラミ(Kluyveromyces wickerhamii)、クルイベロミセス・ヤロウィ(Kluyveromyces yarrowii)等が挙げられる。
 このうち、好ましくは、クルイベロマイセス・サーモトレランス(Kluyveromyces thermotolerans)、クルイベロミセス・ラクティス(Kluyveromyces lactis)及びクルイベロミセス・フラジリス(Kluyveromyces fragilis)、であり、より好ましくはクルイベロマイセス・サーモトレランス(Kluyveromyces thermotolerans)である。
 なお、これらの酵母は、古くからチーズ及びヨーグルト等の乳製品、ワイン、並びに漬物等の発酵食品の製造に使用されている。例えば、クルイベロマイセス・サーモトレランスが、ワイン醸造やプラムジャム発酵物から単離される乳酸産生酵母として、その生化学的性質及び生理的性質と共に報告されている(参考文献1:The Yeasts.A Taxonomic Study,4th ed.Elsevier Science BV,Amsterdam.240-241(1998))。また、クルイベロマイセス・サーモトレランス(Kluyveromyces thermotolerans)として、Kluyveromyces thermotolerans MA KT(NITE BP-1420)菌株が挙げられる。
 このように本開示に用いるクルイベロマイセス属酵母は、人体に対して極めて安全な微生物であり、発酵原料である糖も食することが可能であることから、本開示の成分(A)糖発酵物は安全性が高いと考えられる。
The “Kluyveromyces yeast” used in the present disclosure is not particularly limited, and one or more of the following exemplified yeast species can be selected and used.
Examples of the “Kluyveromyces genus (Kluyveromyces) yeast” include, for example, Kluyveromyces thermotolerans, Kluyveromyces africanus, Kluyveromyces fragilis, Kluyveromyces lactis, Kluyveromyces phaffii, Kluyveromyces waltii, Kluyveromyces wickerhamii, Kluyveromyces wickerhamii, Kluyveromyces warrowhamii Is mentioned.
Of these, Kluyveromyces thermotolerans, Kluyveromyces lactis, and Kluyveromyces fragilis, more preferably Kluyveromyces fragilis. Tolerance (Kluyveromyces thermotolerans).
These yeasts have long been used for producing dairy products such as cheese and yogurt, wine, and fermented foods such as pickles. For example, Kluyveromyces thermotolerance has been reported as a lactic acid-producing yeast isolated from wine brewing and plum jam fermentation products along with its biochemical and physiological properties (Reference 1: The Yeasts.A). Taxonomic Study, 4th ed. Elsevier Science BV, Amsterdam. 240-241 (1998)). Examples of Kluyveromyces thermotolerans include Kluyveromyces thermotolerans MA KT (NITE BP-1420).
Thus, the Kluyveromyces genus yeast used in the present disclosure is an extremely safe microorganism for the human body and can also eat sugar as a fermentation raw material. Therefore, the component (A) sugar of the present disclosure Fermented products are considered to be highly safe.
 本開示の成分(A)糖発酵物の原料に用いる「糖」は、特に限定されず、ショ糖が含まれるものが好ましい。「糖」は、粉体又は液体等のいずれの形態でもよい。
 本開示の成分(A)として、好ましくはサトウキビ由来の糖であり、より好ましくは、サトウキビ茎の搾り汁から得られるサトウキビ糖である。当該サトウキビ由来の糖として、例えば、和三盆、糖蜜、黒蜜、含蜜糖、粗糖、黒糖等の未精製糖;上白糖、グラニュー糖等の精製糖等が挙げられ、これらを1種又は2種以上選択することができる。このうち、上白糖にまで精製されていない未精製糖が好ましく、当該未精製糖のうち、黒糖が好ましい。黒糖は、サトウキビ茎の絞り汁を加熱し、濃縮して製造されたものであり、糖分の分離精製を行なっていないものが好適である。
 本開示の「サトウキビ」は、イネ科サトウキビ属の植物(砂糖黍、学名:Saccharum officinarum)であり、カンショ(甘蔗)ともいう。
The “sugar” used as a raw material for the component (A) fermented sugar of the present disclosure is not particularly limited, and those containing sucrose are preferable. The “sugar” may be in any form such as powder or liquid.
As the component (A) of the present disclosure, sugar derived from sugarcane is preferable, and sugarcane sugar obtained from sugarcane squeezed juice is more preferable. Examples of sugars derived from sugarcane include unpurified sugars such as Wasanbon, molasses, black honey, honey-containing sugar, crude sugar, brown sugar, and the like; and refined sugars such as upper white sugar and granulated sugar. More than one species can be selected. Of these, unpurified sugar that has not been purified to upper white sugar is preferred, and among the unpurified sugars, brown sugar is preferred. Brown sugar is produced by heating and concentrating sugarcane squeezed juice, and is preferably not subjected to separation and purification of sugar.
The “sugarcane” of the present disclosure is a plant belonging to the genus Sugarcane (sugar cane, scientific name: Saccharum officinarum), and is also called sweet potato.
 本開示の成分(A)糖発酵物は、クルイベロマイセス属酵母を糖含有培地にて培養して得た発酵物であるのが好適である。
 本開示の糖含有培地中の糖の含有量は、特に限定されないが、好ましくは3~15質量%、より好ましくは4~8質量%である。
 また、本開示の糖含有培地は液体であるのが好ましい。当該糖含有の液体培地として、例えば、上述した糖と水とを混合した糖水溶液等が挙げられる。当該水としては、特に制限されず、例えば、純水、水道水、井戸水、鉱泉水、鉱水、温泉水、湧水、淡水、精製水、イオン交換水、生理食塩水、リン酸緩衝液、リン酸緩衝生理食塩水等が挙げられる。
 さらに、前記糖含有培地は、通常酵母に使用される培地成分(例えば、炭素源、窒素源、無機塩類等)を含有させたものが、発酵物の生産性向上の点で、好適である。また、前記糖含有培地は、雑菌繁殖を防止する点で、殺菌処理(例えば加熱や膜処理)したものを使用するのが好適である。
The component (A) sugar fermented product of the present disclosure is preferably a fermented product obtained by culturing Kluyveromyces yeast in a sugar-containing medium.
The content of sugar in the sugar-containing medium of the present disclosure is not particularly limited, but is preferably 3 to 15% by mass, more preferably 4 to 8% by mass.
In addition, the sugar-containing medium of the present disclosure is preferably a liquid. Examples of the sugar-containing liquid medium include an aqueous sugar solution obtained by mixing the above-described sugar and water. The water is not particularly limited. For example, pure water, tap water, well water, mineral spring water, mineral water, hot spring water, spring water, fresh water, purified water, ion-exchanged water, physiological saline, phosphate buffer, phosphorus Examples include acid buffered saline.
Furthermore, the sugar-containing medium preferably contains medium components (for example, a carbon source, a nitrogen source, inorganic salts, etc.) usually used for yeast in terms of improving the productivity of the fermented product. In addition, it is preferable to use a saccharide-containing medium that has been sterilized (for example, heated or film-treated) in order to prevent the propagation of various bacteria.
 前記クルイベロマイセス属酵母の培養方法は、通常酵母に使用される培養方法であれば、特に限定されず、公知の手法に従うことができる(例えば、参考文献1参照。)。
 例えば、振盪培養、通気培養、静置培養、撹拌培養等が挙げられる。また、バッチ式や連続式の何れでもよい。これらを単独で又は2種以上組み合わせて行うことができる。
 前記クルイベロマイセス属酵母の培養条件(例えば、好気性、嫌気性、培地中のpH、溶存酸素、培養温度及び培養時間等)は、特に限定されず、目的に応じて適宜選択することができる。
The culture method of the Kluyveromyces genus yeast is not particularly limited as long as it is a culture method usually used for yeast, and can follow a known method (for example, see Reference 1).
For example, shaking culture, aeration culture, stationary culture, stirring culture and the like can be mentioned. Moreover, any of a batch type and a continuous type may be sufficient. These can be performed alone or in combination of two or more.
The culture conditions (for example, aerobic, anaerobic, pH in the medium, dissolved oxygen, culture temperature, culture time, etc.) of the Kluyveromyces yeast are not particularly limited, and can be appropriately selected according to the purpose. it can.
 本開示の成分(A)糖発酵物は、前培養したクルイベロマイセス属酵母を接種した糖含有培地にて好気的培養を行い、調製するのが好適である。このとき、糖含有培地に対して前培養液1%を添加するのが好適である。このとき、培地pHを5~7とし、15~35℃で、1~3日間好気的培養を行うのが好適である。当該好適培養として、好気的条件下にて振盪培養や撹拌培養を行うのが望ましい。なお、好気的条件の場合、空気(酸素20体積%程度)を除菌フィルターで処理したものを使用すればよい。
 また、本開示の調製は、酒類製造のように積極的にエタノール発酵をさせるのではなく、調製終了後の糖発酵物中のエタノール濃度が1質量%未満(好適には0.1質量%以下)となるようにするのが、保湿効果の点で、好適である。
The component (A) fermented sugar of the present disclosure is preferably prepared by aerobic culture in a sugar-containing medium inoculated with pre-cultured Kluyveromyces yeasts. At this time, it is preferable to add 1% of the preculture solution to the sugar-containing medium. At this time, it is preferable to perform the aerobic culture at a medium pH of 5 to 7 at 15 to 35 ° C. for 1 to 3 days. As the preferred culture, it is desirable to perform shaking culture or stirring culture under aerobic conditions. In the case of aerobic conditions, air (about 20% by volume of oxygen) treated with a sterilization filter may be used.
In addition, the preparation of the present disclosure does not actively perform ethanol fermentation as in alcoholic beverage production, but the ethanol concentration in the sugar fermentation product after the preparation is less than 1% by mass (preferably 0.1% by mass or less) ) Is preferable in terms of the moisturizing effect.
 本開示の成分(A)糖発酵物は、上記調製後、そのままの状態で、又は乾燥させた状態で、使用することが可能である。また、本開示の調製後、クルイベロマイセス属酵母の菌体を遠心分離や膜処理等の常法にて除去してもよい。
 また、本開示の成分(A)糖発酵物を、目的に応じて、希釈液、濃縮液、乾燥物としてもよく、さらに分離精製した分離物や精製物としてもよい。希釈する際には、生理食塩液を用いてもよく、乾燥する際には、フリーズドライ方式やスプレイドライ方式を用いてもよい。分離精製する際には、不純物除去等を目的として、遠心分離法、沈殿法、クロマト法等の常法を用いてもよく、脱臭、脱色等を目的として、活性炭、吸着剤、イオン交換樹脂等を用いてもよい。
 また、異なる酵母種で得られた糖発酵物を2種以上混合して使用してもよい。
The component (A) sugar fermented product of the present disclosure can be used as it is or after it is dried. In addition, after preparation of the present disclosure, cells of Kluyveromyces genus yeast may be removed by a conventional method such as centrifugation or membrane treatment.
In addition, the component (A) fermented sugar product of the present disclosure may be a diluted solution, a concentrated solution, or a dried product, and may be a separated product or a purified product according to the purpose. When diluting, a physiological saline solution may be used, and when drying, a freeze drying method or a spray drying method may be used. For separation and purification, conventional methods such as centrifugation, precipitation, and chromatography may be used for the purpose of removing impurities, and activated carbon, adsorbents, ion exchange resins, etc. for the purpose of deodorization and decolorization. May be used.
Moreover, you may use 2 or more types of sugar fermented products obtained with different yeast seed | species.
 本開示に用いられる「成分(B)20℃での比重(g/mL at20℃)が0.93以上の多価アルコール」(以下、「成分(B)多価アルコール」ともいう)について説明する。本開示の成分(B)は、以下の成分(B)多価アルコールの例示から1種又は2種以上選択し、調製することができる。 The “component (B) polyhydric alcohol having a specific gravity at 20 ° C. (g / mL at 20 ° C.) of 0.93 or more” (hereinafter also referred to as “component (B) polyhydric alcohol”) used in the present disclosure will be described. . The component (B) of the present disclosure can be prepared by selecting one or more of the following examples of the component (B) polyhydric alcohol.
 本開示の成分(B)「20℃での比重が0.93以上の多価アルコール」は、メチレングリコール、グルコール(エチレングリコール)、プロピレングリコール、プロパンジオール(1,3-プロパンジオール)、ジエチレングルコール、メチレンプロパンジオール、1,2-ブチレングリコール、1,3-ブチレングリコール、1,4-ブチレングリコール、2,3-ブタンジオール、1,2-ペンタンジオール、1,3-ペンタンジオール、1,4-ペンタンジオール、1,5-ペンタンジオール、2,4-ペンタンジオール、1,2-シクロペンタンジオール、1,3-シクロペンタンジオール、ネオペンチルグリコール、イソペンチルジオール、アミノエチルプロパンジオール、1,2-ヘキサンジオール、1,6-ヘキサンジオール、トリエチレングリコール、ジプロピレングリコール、ブトキシジグリコール、エチルヘキサンジオール、ブチルエチルプロパンジオール、1,10-デカンジオール、エクオール、ポリエチレングリコール、ポリプロピレングリコール、グリセリン、トリメチロールエタン、トリメチロールブタン、1,2,6-ヘキサントリオール、フィタントリオール、ペンタエリスリトール、ジグリセリン、ポリグリセリン等が挙げられる。 Component (B) “polyhydric alcohol having a specific gravity of 0.93 or more at 20 ° C.” of the present disclosure includes methylene glycol, glycol (ethylene glycol), propylene glycol, propanediol (1,3-propanediol), diethylene glycol Coal, methylenepropanediol, 1,2-butylene glycol, 1,3-butylene glycol, 1,4-butylene glycol, 2,3-butanediol, 1,2-pentanediol, 1,3-pentanediol, 1, 4-pentanediol, 1,5-pentanediol, 2,4-pentanediol, 1,2-cyclopentanediol, 1,3-cyclopentanediol, neopentyl glycol, isopentyldiol, aminoethylpropanediol, 1, 2-hexanediol, 1,6-hexanedio , Triethylene glycol, dipropylene glycol, butoxydiglycol, ethylhexanediol, butylethylpropanediol, 1,10-decanediol, equol, polyethylene glycol, polypropylene glycol, glycerin, trimethylolethane, trimethylolbutane, 1, Examples include 2,6-hexanetriol, phytanetriol, pentaerythritol, diglycerin, polyglycerin and the like.
 また、本開示の成分(B)多価アルコールの比重(g/mL at20℃)は、好ましくは1.01以上、より好ましくは1.03以上であるのが、前記成分(A)糖発酵物と併用した際に保湿性をより向上させることができるので、好適である。また、本開示の多価アルコールの比重(g/mL at20℃)は、2以下のものが好ましい。
 前記多価アルコールのアルコール価数は、好ましくは2~4、より好ましくは2~3である。
 前記成分(B)多価アルコールの炭素数は、好ましくは6以下、より好ましくは2~4である。
 前記成分(B)多価アルコールの屈折率は、好ましくは1.3~1.6、より好ましくは1.4~1.5である。
The specific gravity (g / mL at 20 ° C.) of the component (B) polyhydric alcohol of the present disclosure is preferably 1.01 or more, more preferably 1.03 or more. When used together, the moisture retention can be further improved, which is preferable. Moreover, the specific gravity (g / mL at 20 ° C.) of the polyhydric alcohol of the present disclosure is preferably 2 or less.
The alcohol valence of the polyhydric alcohol is preferably 2 to 4, more preferably 2 to 3.
The component (B) polyhydric alcohol preferably has 6 or less carbon atoms, more preferably 2 to 4 carbon atoms.
The refractive index of the component (B) polyhydric alcohol is preferably 1.3 to 1.6, more preferably 1.4 to 1.5.
 前記成分(B)多価アルコールのうち、プロピレングリコール、プロパンジオール、1,2-ブチレングリコール、1,3-ブチレングリコール、1,2-ペンタンジオール、ジプロピレングリコール及びグリセリンが好適である。
 さらに成分(B)のうち、保湿性向上の観点から、プロピレングリコール、プロパンジオール、ジプロピレングリコール及びグリセリンがより好適である。
Of the component (B) polyhydric alcohols, propylene glycol, propanediol, 1,2-butylene glycol, 1,3-butylene glycol, 1,2-pentanediol, dipropylene glycol and glycerin are preferred.
Furthermore, propylene glycol, propanediol, dipropylene glycol and glycerin are more preferable among the components (B) from the viewpoint of improving moisture retention.
 なお、多価アルコールの「20℃での比重」は、日本厚生労働省:医薬部外品原料規格2006(薬事日報社出版)に記載の比重測定法第1法にて測定した値である。
 また、多価アルコールの「20℃の屈折率」は、日本厚生労働省:医薬部外品原料規格2006(薬事日報社出版)に記載の屈折率測定法にて測定した値である。
The “specific gravity at 20 ° C.” of the polyhydric alcohol is a value measured by the specific gravity measurement method No. 1 described in the Ministry of Health, Labor and Welfare: Quasi-drug raw material standard 2006 (published by Yakuji Nipposha).
The “refractive index at 20 ° C.” of the polyhydric alcohol is a value measured by a refractive index measurement method described in Japan Ministry of Health, Labor and Welfare: Quasi-drug raw material standard 2006 (published by Yakuji Nippo).
 本開示の保湿剤の調製は、前記成分(A)糖発酵物と前記成分(B)多価アルコールとを組み合わせるため、これらを混合させればよい。これらを組み合わせる際に、前記成分(A)糖発酵物は糖発酵液(好適には水溶液)を用いるのが好ましい。
 本開示の保湿剤における前記成分(A)糖発酵物と前記成分(B)多価アルコールの含有比率(乾燥固形分の質量部:質量部)は、特に限定されないが、保湿性向上の観点から、好ましくは0.09:0.5~0.09:30、より好ましくは0.09:1~0.09:20、さらに好ましくは0.09:5~0.09:10である。
 また、保湿剤中の前記成分(B)多価アルコールの含有量は、好ましくは1~30質量%、より好ましくは5~20質量%とするのが、好適である。なお、水を用いて保湿剤100質量%になるように調整することが可能である。
 また、得られる本開示の保湿剤の形態は特に限定されないが、液状又は半固形状が好ましい。
The preparation of the humectant of the present disclosure combines the component (A) sugar fermented product and the component (B) polyhydric alcohol, and therefore, these may be mixed. When combining these, it is preferable to use a sugar fermentation liquid (preferably an aqueous solution) as the component (A) sugar fermentation product.
The content ratio of the component (A) sugar fermented product and the component (B) polyhydric alcohol in the moisturizing agent of the present disclosure (parts by mass of dry solids: parts by mass) is not particularly limited, but from the viewpoint of improving moisturizing properties. The ratio is preferably 0.09: 0.5 to 0.09: 30, more preferably 0.09: 1 to 0.09: 20, and still more preferably 0.09: 5 to 0.09: 10.
In addition, the content of the component (B) polyhydric alcohol in the moisturizing agent is preferably 1 to 30% by mass, more preferably 5 to 20% by mass. In addition, it is possible to adjust so that it may become 100 mass% of humectants using water.
Moreover, the form of the moisturizing agent of the present disclosure to be obtained is not particularly limited, but liquid or semi-solid is preferable.
 後記実施例に示すように、前記成分(A)糖発酵物及び前記成分(B)多価アルコールを含有させることによって、それぞれ単独の場合と比較して、保湿性が飛躍的に向上することが認められた。よって、前記成分(A)及び前記成分(B)の混合物は、非常に優れた保湿性を有することから、保湿のために使用してもよく、また保湿のための使用を目的とした各種製剤に使用することができ、これら各種製剤を製造するために使用することも可能である。
 また、前記成分(A)及び前記成分(B)の組み合わせは、優れた保湿性を有するので、保湿によって、皮膚に関する各種症状や状態等の予防、改善及び/又は治療を図るための方法に使用することができる。この各種症状や状態としては、例えば、肌荒れ、シワ形成、皮膚老化、乾皮症、フケ症、等が挙げられる。また、前記成分(A)及び前記成分(B)の組み合わせは、対象物(例えば、皮膚、毛髪、食品等)にしっとり感を付与させることができる。例えば、前記成分(A)及び前記成分(B)の組み合わせは、毛髪にしっとり感やまとまり感を付与するために使用することができ、これにより、毛髪のぱさつき抑えることができる。
 従って、前記成分(A)糖発酵物及び前記成分(B)多価アルコールは、保湿性を向上又は付与させるために、皮膚外用剤、化粧料、医薬部外品、医薬品、食品や機能性食品(例えば特定保健用食品)等(以下、「製剤」ともいう)等に含有させることが可能である。本開示の保湿剤は、上述の皮膚外用剤、化粧料、食品等とすることができる。また、本開示の前記成分(A)及び前記成分(B)を含有する保湿剤をこれら製剤に含有させてもよい。
As shown in the below-mentioned Examples, by containing the component (A) fermented sugar and the component (B) polyhydric alcohol, the moisture retention can be dramatically improved as compared with the case where each component is used alone. Admitted. Therefore, since the mixture of the component (A) and the component (B) has a very excellent moisturizing property, it may be used for moisturizing and various preparations intended for use for moisturizing. It can also be used to produce these various formulations.
Moreover, since the combination of the said component (A) and the said component (B) has the outstanding moisturizing property, it is used for the method for aiming at prevention, improvement, and / or treatment of various symptoms, conditions, etc. regarding skin by moisturizing. can do. Examples of the various symptoms and conditions include rough skin, wrinkle formation, skin aging, xeroderma, dandruff, and the like. Moreover, the combination of the said component (A) and the said component (B) can give a moist feeling to a target object (for example, skin, hair, foodstuff, etc.). For example, the combination of the said component (A) and the said component (B) can be used in order to give a moist feeling and a feeling of unity to hair, and, thereby, can suppress hairiness.
Therefore, the component (A) sugar fermented product and the component (B) polyhydric alcohol are used in order to improve or impart moisturizing properties, such as external preparations for skin, cosmetics, quasi drugs, pharmaceuticals, foods and functional foods. (For example, food for specified health use) and the like (hereinafter also referred to as “formulation”) and the like. The moisturizing agent of the present disclosure can be the above-mentioned external preparation for skin, cosmetics, foods and the like. Moreover, you may make these preparations contain the moisturizer containing the said component (A) of this indication, and the said component (B).
 本開示の保湿剤又は前記成分(A)糖発酵物及び前記成分(B)多価アルコールは、特に皮膚外用剤、化粧料、医薬部外品等に用いるのが好適であり、皮膚及び毛髪に塗布等接触させる製剤が好適である。皮膚外用剤、化粧料として、例えば、化粧水、乳液(水中油型等)、クリーム(水中油型)、パック化粧料、リキッドファンデーション、軟膏剤、養毛料、毛髪保護料等が挙げられる。 The humectant of the present disclosure or the component (A) fermented sugar and the component (B) polyhydric alcohol are particularly suitable for use in external preparations for skin, cosmetics, quasi drugs, etc. A preparation to be contacted by application or the like is preferable. Examples of skin external preparations and cosmetics include skin lotions, emulsions (oil-in-water type, etc.), creams (oil-in-water type), pack cosmetics, liquid foundations, ointments, hair nourishing agents, hair protectants and the like.
 本開示の製剤中の前記成分(A)糖発酵物の含有量は、製剤の安定性及び保湿性の観点から、乾燥固形分として、好ましくは0.001~0.095質量%、より好ましくは0.005~0.05質量%、さらに好ましくは0.001~0.02質量%である。
 本開示の製剤中の前記成分(B)多価アルコールの含有量は、安全性及び保湿性の観点から好ましくは1~50質量%、より好ましくは5~40質量%、さらに好ましくは10~30質量%である。
 本開示の製剤における前記成分(A)糖発酵物及び前記成分(B)多価アルコールの含有比率(乾燥固形分の質量部:質量部)は、特に限定されないが、製剤の安定性及び保湿性の観点から、好ましくは0.01:5~0.01:500、より好ましくは0.01:10~0.01:300、さらに好ましくは0.01:20~0.01:200である。
The content of the component (A) fermented sugar in the preparation of the present disclosure is preferably 0.001 to 0.095% by mass, more preferably as a dry solid content, from the viewpoint of the stability of the preparation and moisture retention. It is 0.005 to 0.05 mass%, more preferably 0.001 to 0.02 mass%.
The content of the component (B) polyhydric alcohol in the preparation of the present disclosure is preferably 1 to 50% by mass, more preferably 5 to 40% by mass, and further preferably 10 to 30% from the viewpoints of safety and moisture retention. % By mass.
The content ratio of the component (A) sugar fermented product and the component (B) polyhydric alcohol in the formulation of the present disclosure (parts by mass of dry solids: parts by mass) is not particularly limited, but the stability and moisture retention of the formulation From this viewpoint, it is preferably 0.01: 5 to 0.01: 500, more preferably 0.01: 10 to 0.01: 300, and still more preferably 0.01: 20 to 0.01: 200.
 なお、本開示の保湿剤及び本開示の製剤には、本開示の前記成分(A)糖発酵物及び前記成分(B)多価アルコールの他、本技術の効果を損ねない範囲で、必要に応じて任意の成分を組み合わせて使用してもよい。他の成分としては、薬学的に許容される成分であればよく、例えば、防腐剤、細胞賦活剤、抗酸化剤、保湿剤、紫外線防止剤、溶剤(水、アルコール類等)、油剤、界面活性剤、増粘剤、粉体、キレート剤、pH調整剤、乳化剤、安定化剤、着色剤、光沢剤、矯味剤、矯臭剤、賦形剤、結合剤、崩壊剤、滑沢剤、希釈剤、浸透圧調整剤、香料等が挙げられ、これらを目的とする製剤に応じて配合すればよい。
 また、前記製剤の形態は、特に限定されず、液状、ペースト状、ゲル状、固形状、粉末状等の何れの形態でもよい。
In addition, the moisturizer of the present disclosure and the preparation of the present disclosure are necessary as long as the effects of the present technology are not impaired in addition to the component (A) fermented sugar and the component (B) polyhydric alcohol of the present disclosure. Depending on the situation, optional components may be used in combination. Other components may be pharmaceutically acceptable components, such as preservatives, cell activators, antioxidants, humectants, UV inhibitors, solvents (water, alcohols, etc.), oils, interfaces Activator, Thickener, Powder, Chelating agent, pH adjuster, Emulsifier, Stabilizer, Colorant, Brightener, Flavoring agent, Flavoring agent, Excipient, Binder, Disintegrant, Lubricant, Dilution Agents, osmotic pressure adjusting agents, fragrances and the like, and these may be added according to the intended preparation.
The form of the preparation is not particularly limited, and may be any form such as liquid, paste, gel, solid, and powder.
 なお、本技術は、以下の構成を採用することも可能である。
〔1〕 次の成分(A)及び(B);
 (A)クルイベロマイセス属の酵母による糖発酵物
 (B)20℃での比重が0.93以上の多価アルコール
を含有する保湿剤。
〔2〕 前記糖発酵物が、サトウキビ糖由来の発酵物である前記〔1〕記載の保湿剤。
〔3〕 前記糖発酵物が、エタノール濃度1質量%未満のものである前記〔1〕又は〔2〕記載の保湿剤。
〔4〕 成分(B)の多価アルコールが、20℃での比重が1.01以上の多価アルコールである、前記〔1〕~〔3〕の何れか1項記載の保湿剤。
〔5〕 成分(B)の多価アルコールが、グリセリン、プロパンジオール、プロピレングリコール、ジプロピレングリコールから選ばれる1種又は2種以上のものである前記〔1〕~〔4〕の何れか1項記載の保湿剤。
In addition, this technique can also employ | adopt the following structures.
[1] The following components (A) and (B);
(A) Sugar fermented product from yeast of the genus Kluyveromyces (B) A humectant containing a polyhydric alcohol having a specific gravity at 20 ° C. of 0.93 or more.
[2] The humectant according to [1], wherein the sugar fermentation product is a fermentation product derived from sugarcane sugar.
[3] The humectant according to [1] or [2], wherein the fermented sugar product has an ethanol concentration of less than 1% by mass.
[4] The humectant according to any one of [1] to [3], wherein the polyhydric alcohol of component (B) is a polyhydric alcohol having a specific gravity at 20 ° C. of 1.01 or more.
[5] Any one of [1] to [4], wherein the polyhydric alcohol of component (B) is one or more selected from glycerin, propanediol, propylene glycol, and dipropylene glycol. The humectant described.
〔6〕 前記クルイベロマイセス属の酵母が、クルイベロマイセス・サーモトレランス(Kluyveromyces thermotolerans)、クルイベロミセス・ラクティス(Kluyveromyces lactis)及びクルイベロミセス・フラジリス(Kluyveromyces fragilis)から選ばれる1種又は2種以上のものである前記〔1〕~〔5〕の何れか1項記載の保湿剤。
〔7〕成分(A)糖発酵物は、クルイベロマイセス属酵母を糖(好適には未精製糖)含有培地にて培養して得た発酵物である前記〔1〕~〔6〕の何れか1項記載の保湿剤。
[6] The yeast belonging to the genus Kluyveromyces is one selected from Kluyveromyces thermotolerans, Kluyveromyces lactis and Kluyveromyces fragilis The humectant according to any one of [1] to [5], which is two or more kinds.
[7] The component (A) fermented sugar product is a fermented product obtained by culturing Kluyveromyces yeast in a sugar (preferably unpurified sugar) -containing medium. The humectant according to any one of the above.
 以下、実施例、参考例、比較例、試験例、製造例等を挙げ、本発明(本技術)をさらに具体的に説明するが、本発明(本技術)はこれら実施例等に何ら制約されるものではない。 Examples, Reference Examples, Comparative Examples, Test Examples, Production Examples, etc. are given below to describe the present invention (present technique) more specifically. However, the present invention (present technique) is not limited to these examples. It is not something.
<調製例1:クルイベロマイセス・サーモトレランス(Kluyveromyces thermotolerans)による黒糖発酵液の調製>
〔前培養〕
 クルイベロマイセス・サーモトレランス MA KT(NITE BP-1420)をYPD培地(pH6.0)を用いて液体培養を行った。前記液体培養液を1白金耳とり、YM培地(固体培地)に植菌し、2日間、25℃で前培養を行った。なお、YPD(Yeast Extract-Peptone-Dextrose)培地及びYM(Yeast Mold)培地は、DifcoTM&BBLTM Manual,2nd Editionに記載されている内容に従って作成したものである。
 Kluyveromyces thermotoleransMA KT(NITE BP-1420)菌株は、原産国:日本/分離源:樹液で採取され、形態観察及び細菌学的性質からLachancea (Kluyveromyces) thermotoleransと分類され、MA KT菌株と命名されたものである。当該菌株は、寄託先:〒292-0818 千葉県木更津市かずさ鎌足2-5-8、独立行政法人 製品評価技術基盤機構 特許微生物寄託センター(NPMD)に、2012年9月13日に寄託されているものである。
<Preparation Example 1: Preparation of brown sugar fermentation broth by Kluyveromyces thermotolerans>
[Pre-culture]
Liquid culture of Kluyveromyces thermotolerance MA KT (NITE BP-1420) was performed using YPD medium (pH 6.0). One platinum loop of the liquid culture solution was taken and inoculated into a YM medium (solid medium), and precultured at 25 ° C. for 2 days. Incidentally, YPD (Yeast Extract-Peptone- Dextrose) medium and YM (Yeast Mold) media are those made in accordance with what is described in Difco TM & BBL TM Manual, 2 nd Edition.
Kluyveromyces thermotolerans MA KT (NITE BP-1420) is a country of origin: Japan / source: collected from sap, classified as Lachancea (Kluyveromyces) thermotolerans based on morphology and bacteriological properties, and named MA KT It is. The strain was deposited on September 13, 2012 at the depository: 2-5-8, Kazusa Kamashichi, Kisarazu City, Chiba Prefecture 292-0818, Japan, and the National Institute of Technology and Technology (NPMD). It is what.
〔黒糖水溶液の調製〕
 黒糖25質量部に純水500質量部を添加し、5質量%黒糖水溶液とした。前記5質量%黒糖水溶液を、通気攪拌型発酵槽とともに殺菌後、適温に調節した。
 黒糖として、サトウキビ茎の絞り汁を加熱し、濃縮して製造された市販品を使用した。
[Preparation of brown sugar aqueous solution]
500 parts by mass of pure water was added to 25 parts by mass of brown sugar to obtain a 5% by mass brown sugar aqueous solution. The 5 mass% brown sugar aqueous solution was sterilized together with the aeration and stirring type fermenter, and then adjusted to an appropriate temperature.
As brown sugar, a commercial product produced by heating and concentrating sugarcane stem juice was used.
〔発酵工程〕
 前記クルイベロマイセス・サーモトレランス(Kluyveromyces thermotolerans)の前培養により得られたコロニーを生理的食塩水で懸濁して、1.0×10CFU/mL~1.0×1010CFU/mLとなるよう調製した懸濁液を、前記5質量%黒糖水溶液に、前記5質量%黒糖水溶液の全量の1質量%を添加し、30℃で2日間、振とう培養(振とう条件:100rpm)を行った。振とう培養後の培養液をオートクレーブ(条件:121℃、15分)で滅菌した後、ろ過により不純物や残渣物などを除去した。その後、精製水とフェノキシエタノールを添加し、固形分濃度0.1質量%の、クルイベロマイセス・サーモトレランス(Kluyveromyces thermotolerans)の黒糖発酵液を調製した。エタノール含量は0.01%であった。
[Fermentation process]
A colony obtained by pre-culture of the Kluyveromyces thermotolerans was suspended in physiological saline to obtain 1.0 × 10 9 CFU / mL to 1.0 × 10 10 CFU / mL. 1% by mass of the total amount of the 5% by mass brown sugar aqueous solution is added to the 5% by mass brown sugar aqueous solution, and the shaking suspension (shaking condition: 100 rpm) is performed at 30 ° C. for 2 days. went. The culture solution after shaking culture was sterilized with an autoclave (conditions: 121 ° C., 15 minutes), and then impurities and residues were removed by filtration. Thereafter, purified water and phenoxyethanol were added to prepare a brown sugar fermentation broth of Kluyveromyces thermotolerans having a solid concentration of 0.1% by mass. The ethanol content was 0.01%.
<実施例1~7及び比較例1、2:保湿剤の製造>
 調製例1にて調製した黒糖発酵液が固形分濃度0.09質量%及び表1に示す各多価アルコールが10質量%となるよう混合し、実施例1~7及び比較例1~2の保湿剤を製造した。また、黒糖発酵液の代わりに精製水を混合した試料も調整した。
 比重は、日本厚生労働省:医薬部外品原料規格2006(薬事日報社出版)に記載の比重測定法第1法にて測定した。
 屈折率は、日本厚生労働省:医薬部外品原料規格2006(薬事日報社出版)に記載の屈折率測定法にて測定した。
無印:医薬部外品原料規格2006
#1 MERCK INDEX ELEVENTH EDITION
#2 化学便覧基礎編I(日本化学会改訂4版)
#3 化粧品ハンドブック(日光ケミカルズ)
#4 Chemical book
<Examples 1 to 7 and Comparative Examples 1 and 2: Production of moisturizing agent>
The brown sugar fermentation broth prepared in Preparation Example 1 was mixed so that the solid content concentration was 0.09% by mass and each polyhydric alcohol shown in Table 1 was 10% by mass, and Examples 1 to 7 and Comparative Examples 1 to 2 were mixed. A humectant was produced. Moreover, the sample which mixed the purified water instead of the brown sugar fermentation liquid was also prepared.
The specific gravity was measured by the specific gravity measurement method No. 1 described in Japan Ministry of Health, Labor and Welfare: Quasi-drug raw material standard 2006 (published by Yakuji Nippo Co., Ltd.).
The refractive index was measured by the refractive index measurement method described in the Ministry of Health, Labor and Welfare: quasi-drug raw material standard 2006 (published by Yakuji Nippo Co., Ltd.).
No symbol: Quasi-drug raw material standard 2006
# 1 MERCK INDEX ELEVENTH EDITION
# 2 Chemical Handbook Basics I (The Chemical Society of Japan, revised 4th edition)
# 3 Cosmetics Handbook (Nikko Chemicals)
# 4 Chemical book
 保湿効果は、下記の方法により測定した。
前腕内側部を洗浄後、測定部位(2cm×2cm)をマーキングした。気温20℃、湿度50%下にて20分馴化し、Skicon200(I.B.S.Co.Ltd.)にて水分量を測定した。この値を塗布前の値とした。その後、2cm×2cmのティッシュペーパーに試料を100μL含浸させてから、測定部位にのせ、5分間静置した。ティッシュペーパーを剥がして、指で試料を皮膚に塗布した。塗布完了から60分後にSkicon200(I.B.S.Co.Ltd.)にて水分量を測定した値を60分後の値とした。
The moisturizing effect was measured by the following method.
After washing the inner part of the forearm, the measurement site (2 cm × 2 cm) was marked. It was acclimatized for 20 minutes under an air temperature of 20 ° C. and a humidity of 50%, and the moisture content was measured with Skicon200 (IBSCo. Ltd.). This value was taken as the value before coating. Thereafter, 100 μL of the sample was impregnated into a 2 cm × 2 cm tissue paper, and then placed on the measurement site and allowed to stand for 5 minutes. The tissue paper was peeled off and the sample was applied to the skin with a finger. The value obtained by measuring the moisture content with Skicon200 (IBSCo. Ltd.) 60 minutes after the completion of coating was taken as the value after 60 minutes.
Figure JPOXMLDOC01-appb-T000001
 
Figure JPOXMLDOC01-appb-T000001
 
 保湿試験の結果を図1及び図2に示した。
 黒糖発酵液と多価アルコールの混合液を塗布したときをs、黒糖発酵液と精製水の混合液を塗布したときをwとし、塗布60分後の水分量をA、 塗布前の水分量をBとした。
このときのAs/Bs及びAw/Bwを図1に示した。また、(As/Bs)/(Aw/Bw)を図2に示した。
 黒糖発酵液と精製水とを組み合わせた比較例2では、塗布前に比べて水分量は低下したが、黒糖発酵液と20℃での比重が0.93以上の多価アルコールとを組み合わせた実施例1~7では、塗布60分後まで水分量が高く保たれていた。
 すなわち、クルイベロマイセス属の酵母による糖発酵物と20℃での比重が0.93以上の多価アルコールとを組み合わせることによって、それぞれを単独で使用する場合と比較して、飛躍的に保湿性が向上することが認められた。多価アルコールの比重が1.0065を超えることによって、より保湿性が顕著に向上することが認められた。
The results of the moisture retention test are shown in FIGS.
S is the time when the mixed solution of brown sugar fermented liquid and polyhydric alcohol is applied, w is the time when the mixed liquid of brown sugar fermented liquid and purified water is applied, the water content after 60 minutes of application is A, and the water content before coating B.
As / Bs and Aw / Bw at this time are shown in FIG. Further, (As / Bs) / (Aw / Bw) is shown in FIG.
In Comparative Example 2 in which brown sugar fermented liquid and purified water were combined, the amount of water was lower than before application, but the brown sugar fermented liquid was combined with polyhydric alcohol having a specific gravity of 0.93 or higher at 20 ° C. In Examples 1 to 7, the water content was kept high until 60 minutes after application.
That is, by combining a sugar fermentation product from yeast of the genus Kluyveromyces with a polyhydric alcohol having a specific gravity of 0.93 or higher at 20 ° C., the moisture content is dramatically increased compared to the case where each is used alone. It was observed that the sex was improved. It was recognized that the moisture retention was significantly improved when the specific gravity of the polyhydric alcohol exceeded 1.0065.
〔処方例1:可溶化型化粧水〕
(成分)                        (質量%)
1.POE(40モル)硬化ヒマシ油            0.5
2.POE(12モル)ジオレエート            0.3
3.アスタキサンチン                   0.025
4.1,3-ブチレングリコール              2.0
5.グリセリン                      2.0
6.エタノール                     15.0
7.トラネキサム酸                    2.0
8.調製例1の黒糖発酵液(固形分濃度0.1質量%)   10.0
9.乳酸ナトリウム                    0.2
10.パラオキシ安息香酸メチル              0.1
11.精製水                       残 量
 
(製造方法)
A.成分1~6を混合溶解する。
B.成分7~11を混合溶解する。
C.BにAを加え、化粧水を得た。
 本処方例1の化粧水は、肌に潤いを与え、長時間にわたって皮膚の乾燥を防ぎ、保湿効果に優れたものであった。
[Prescription Example 1: Solubilized lotion]
(Ingredient) (mass%)
1. POE (40 mol) hydrogenated castor oil 0.5
2. POE (12 mol) dioleate 0.3
3. Astaxanthin 0.025
4.1,3-Butylene glycol 2.0
5. Glycerin 2.0
6). Ethanol 15.0
7). Tranexamic acid 2.0
8). Brown sugar fermentation broth of Preparation Example 1 (solid content concentration 0.1% by mass) 10.0
9. Sodium lactate 0.2
10. Methyl paraoxybenzoate 0.1
11. Purified water balance
(Production method)
A. Components 1 to 6 are mixed and dissolved.
B. Components 7 to 11 are mixed and dissolved.
C. A was added to B to obtain a skin lotion.
The skin lotion of the present Formulation Example 1 moisturized the skin, prevented the skin from drying for a long time, and was excellent in the moisturizing effect.
〔処方例2:乳化化粧水〕
(成分)                        (質量%)
1.大豆由来水素添加リン脂質               0.5
2.セトステアリルアルコール               0.1
3.ポリオキシエチレン(10モル)コレステロールエーテル 0.2
4.酢酸-dl-α-トコフェロール            0.1
5.スクワラン                      0.1
6.ヒドロキシエチルセルロース              0.03
7.精製水                        残量
8.コウジ酸                       2.0
9.調製例1の黒糖発酵液(固形分濃度0.1質量%)    5.0
10.リン酸一水素二ナトリウム              0.1
11.リン酸二水素一ナトリウム              0.1
12.グリセリン                     3.0
13.ジプロピレングリコール               2.0
14.エタノール                     7.0
15.香料                        適量
 
(製造方法)
A.成分1~5を75℃に加熱し、均一に混合溶解する。
B.成分6、7を75℃に加熱し、均一に混合溶解する
C.AにBを添加し、乳化する。
D.Cを冷却し、成分8~15を添加し、乳化型化粧水を得た。
 本処方例2の化粧水は、肌に潤いを与え、長時間にわたって皮膚の乾燥を防ぎ、保湿効果に優れたものであった。
[Formulation Example 2: Emulsion lotion]
(Ingredient) (mass%)
1. Soybean-derived hydrogenated phospholipid 0.5
2. Cetostearyl alcohol 0.1
3. Polyoxyethylene (10 mol) cholesterol ether 0.2
4). Acetic acid-dl-α-tocopherol 0.1
5. Squalane 0.1
6). Hydroxyethyl cellulose 0.03
7). Purified water remaining amount 8. Kojic acid 2.0
9. Brown sugar fermentation broth of Preparation Example 1 (solid content concentration 0.1% by mass) 5.0
10. Disodium monohydrogen phosphate 0.1
11. Monosodium dihydrogen phosphate 0.1
12 Glycerin 3.0
13. Dipropylene glycol 2.0
14 Ethanol 7.0
15. Perfume
(Production method)
A. Ingredients 1 to 5 are heated to 75 ° C. and mixed and dissolved uniformly.
B. Ingredients 6 and 7 are heated to 75 ° C. and mixed and dissolved uniformly. Add B to A and emulsify.
D. C was cooled and ingredients 8 to 15 were added to obtain an emulsified lotion.
The lotion of the present Formulation Example 2 moisturized the skin, prevented the skin from drying for a long time, and was excellent in the moisturizing effect.
〔処方例3:乳液〕
(成分)                        (質量%)
1.モノオレイン酸ポリオキシエチレン(20)ソルビタン  1.0
2.セスキオレイン酸ソルビタン              0.5
3.トリオクタン酸グリセリル               0.5
4.ホホバ油                       0.5
5.スクワラン                      0.5
6.精製水                         残量
7.エデト酸二ナトリウム                 0.1
8.メチルパラベン                    0.2
9.フェノキシエタノール                 0.5
10.グリセリン                     5.0
11.プロパンジオール                  1.0
12.プロピレングリコール                2.0
13.乳酸ナトリウム                   0.5
14.2-O-α-D-グルコシル-L-アスコルビン酸   1.0
15.調製例1の黒糖発酵液(固形分濃度0.1質量%)  20.0
16.キサンタンガム                   0.05
17.精製水                      10.0
18.エタノール                     3.0
19.香料                         適量
 
(製造方法)
A:成分16を70℃に加熱した成分17で膨潤する。   
B:成分1~5を70℃で加熱混合する。   
C:成分6~13を70℃で加熱溶解後、Bに添加し、乳化する。   
D:Cを室温まで冷却後、成分14、15、18とAを添加し、美容液を得た。 
 本処方例3の乳液は、肌に潤いを与え、長時間にわたって皮膚の乾燥を防ぎ、保湿効果に優れたものであった。
[Prescription Example 3: Latex]
(Ingredient) (mass%)
1. Polyoxyethylene (20) sorbitan monooleate 1.0
2. Sorbitan sesquioleate 0.5
3. Glyceryl trioctanoate 0.5
4). Jojoba oil 0.5
5. Squalane 0.5
6). 6. Purified water remaining amount Edetate disodium 0.1
8). Methylparaben 0.2
9. Phenoxyethanol 0.5
10. Glycerin 5.0
11. Propanediol 1.0
12 Propylene glycol 2.0
13. Sodium lactate 0.5
14. 2-O-α-D-glucosyl-L-ascorbic acid 1.0
15. Brown sugar fermentation broth of Preparation Example 1 (solid content concentration 0.1% by mass) 20.0
16. Xanthan gum 0.05
17. Purified water 10.0
18. Ethanol 3.0
19. Perfume
(Production method)
A: Swell component 16 with component 17 heated to 70 ° C.
B: Components 1 to 5 are heated and mixed at 70 ° C.
C: Components 6 to 13 are dissolved by heating at 70 ° C., then added to B and emulsified.
D: After cooling C to room temperature, ingredients 14, 15, 18 and A were added to obtain a cosmetic liquid.
The emulsion of this Formulation Example 3 moisturized the skin, prevented the skin from drying for a long time, and was excellent in the moisturizing effect.
〔処方例4:養毛料〕
(成分)                        (質量%)
1.スエルチアニン                    1.5
2.イチョウエキス                    0.5
3.グリチルリチン酸ジカリウム              0.1
4.調製例1の黒糖発酵液 (固形分濃度0.1質量%)   1.0
5.グリセリン                      2.0
6.精製水                        残量
7.D-パントテニルアルコール              0.3
8.ヒノキチオール                    0.02
9.セファランチン                    0.001
10.酢酸トコフェロール                 0.01
11.L-メントール                   0.2
12.ポリオキシエチレン硬化ヒマシ油           0.2
13.エタノール                    60
(製造方法)
A.成分1~6を混合溶解する。
B.成分7~11を混合溶解する。
C.AにBを加え、養毛料を得た。
 本処方例4の養毛料は、頭皮・頭髪に潤いを与え、長時間にわたって乾燥を防ぎ、保湿効果に優れたものであった。
[Formulation Example 4: Hair Nourishing]
(Ingredient) (mass%)
1. Srutianin 1.5
2. Ginkgo biloba extract 0.5
3. Dipotassium glycyrrhizinate 0.1
4). Brown sugar fermentation liquid of Preparation Example 1 (solid content concentration 0.1% by mass) 1.0
5. Glycerin 2.0
6). 6. Purified water remaining amount D-pantothenyl alcohol 0.3
8). Hinokitiol 0.02
9. Cephalanthin 0.001
10. Tocopherol acetate 0.01
11. L-Menthol 0.2
12 Polyoxyethylene hydrogenated castor oil 0.2
13. Ethanol 60
(Production method)
A. Components 1 to 6 are mixed and dissolved.
B. Components 7 to 11 are mixed and dissolved.
C. B was added to A to obtain a hair nourishing agent.
The hair nourishing agent of Prescription Example 4 moisturized the scalp and hair, prevented drying over a long period of time, and was excellent in moisturizing effect.
〔処方例5:毛髪トリートメント〕
(成分)                       (質量%)
1.精製水                       残量
2.エタノール                    10.0
3.プロピレングリコール                2.0
4.リン酸1水素ナトリウム               0.03
5.ヒドロキシエチルセルロース             0.01
6.エタノール                     5.0
7.塩化ステアリルトリメチルアンモニウム        0.32
8.ホホバ油                      0.01
9.椿油                        0.01
10.パラメトキシケイヒ酸2-エチルヘキシル      0.2
11.ミリスチン酸イソプロピル             0.2
12.パラオキシ安息香酸メチル             0.05
13.イソステアリン酸ポリオキシエチレン硬化ヒマシ油  0.5
14.ピロリドン酸カルボン酸ナトリウム         0.1
15.ソルビトール                   0.3
16.調製例1の黒糖発酵液(固形分濃度0.1質量%)  3.0
17.精製水                      1.0
 
(製造方法)
A.成分1~5を混合溶解する。
B.成分6~13を混合溶解する。
C.AにBを加え、14~17を添加して毛髪トリートメントを得た。
 本処方例5の毛髪トリートメントは、頭皮・頭髪に潤いを与え、長時間にわたって乾燥を防ぎ、毛髪をしっとりさせ、まとまり感を付与する効果に優れたものであった。
[Prescription Example 5: Hair Treatment]
(Ingredient) (mass%)
1. 1. Purified water remaining amount Ethanol 10.0
3. Propylene glycol 2.0
4). Sodium monohydrogen phosphate 0.03
5. Hydroxyethyl cellulose 0.01
6). Ethanol 5.0
7). Stearyltrimethylammonium chloride 0.32
8). Jojoba oil 0.01
9. Rice bran oil 0.01
10. 2-Ethylhexyl paramethoxycinnamate 0.2
11. Isopropyl myristate 0.2
12 Methyl paraoxybenzoate 0.05
13. Isostearic acid polyoxyethylene hydrogenated castor oil 0.5
14 Sodium pyrophosphate acid 0.1
15. Sorbitol 0.3
16. Brown sugar fermentation broth of Preparation Example 1 (solid content concentration 0.1% by mass) 3.0
17. Purified water 1.0

(Production method)
A. Ingredients 1 to 5 are mixed and dissolved.
B. Components 6 to 13 are mixed and dissolved.
C. Hair treatment was obtained by adding B to A and adding 14-17.
The hair treatment of Formulation Example 5 was excellent in the effect of moisturizing the scalp and hair, preventing drying over a long period of time, moistening the hair, and giving a sense of unity.
〔処方例6:軟膏A〕
(配合成分)                    (質量%)
1.ステアリルアルコール               18.0
2.モクロウ                     20.0
3.ポリオキシエチレン(20)モノオレイン酸エステル  0.25
4.グリセリンモノステアリン酸エステル         0.3
5.ワセリン                     40.0
6.精製水                       残量
7.グリセリン                    10.0
8.1,2-ペンタンジオール              2.0
9.調製例1の黒糖発酵液(固形分濃度0.1質量%)  15.0
 
(製造方法)
A.1~5を70℃で均一に混合する。
B.6~8を70℃に加温する。
C.AにBを加え、乳化する。
D.Cを冷却し、9を添加し、軟膏を得た。
 本処方例6の軟膏は、肌に潤いを与え、長時間にわたって皮膚の乾燥を防ぎ、保湿効果に優れたものであった。
[Prescription Example 6: Ointment A]
(Compounding ingredients) (mass%)
1. Stearyl alcohol 18.0
2. Owl 20.0
3. Polyoxyethylene (20) monooleate 0.25
4). Glycerin monostearate 0.3
5. Vaseline 40.0
6). 6. Purified water remaining amount Glycerin 10.0
8.1,2-Pentanediol 2.0
9. Brown sugar fermentation broth of Preparation Example 1 (solid content concentration 0.1% by mass) 15.0

(Production method)
A. Mix 1-5 uniformly at 70 ° C.
B. Warm 6-8 to 70 ° C.
C. Add B to A and emulsify.
D. C was cooled and 9 was added to obtain an ointment.
The ointment of Formulation Example 6 moisturized the skin, prevented the skin from drying for a long time, and was excellent in the moisturizing effect.
 MA KT(NITE BP-1420)菌株/分類:Lachancea (Kluyveromyces) thermotolerans/寄託先:〒292-0818 千葉県木更津市かずさ鎌足2-5-8、独立行政法人 製品評価技術基盤機構 特許微生物寄託センター(NPMD)/受託日:2012年9月13日。 MA KT (NITE BP-1420) strain / Classification: Lachancea (Kluyveromyces) thermotolerans / Depositary: 292-0818, Kisarazu City, Chiba Pref. (NPMD) / Contract date: September 13, 2012.

Claims (4)

  1.  次の成分(A)及び(B);
    (A)クルイベロマイセス属の酵母による糖発酵物
    (B)20℃での比重が0.93以上の多価アルコール
    を含有する保湿剤。
    The following components (A) and (B);
    (A) Sugar fermented product from yeast of the genus Kluyveromyces (B) A humectant containing a polyhydric alcohol having a specific gravity at 20 ° C. of 0.93 or more.
  2.  前記糖発酵物が、サトウキビ由来の糖発酵物である請求項1記載の保湿剤。 The humectant according to claim 1, wherein the sugar fermentation product is a sugar fermentation product derived from sugarcane.
  3.  成分(B)の多価アルコールが、20℃での比重が1.01以上の多価アルコールである請求項1又は2記載の保湿剤。 The humectant according to claim 1 or 2, wherein the polyhydric alcohol of component (B) is a polyhydric alcohol having a specific gravity at 20 ° C of 1.01 or more.
  4.  成分(B)の多価アルコールが、グリセリン、プロパンジオール、プロピレングリコール、ジプロピレングリコールから選ばれる1種又は2種以上のものである請求項1~3の何れか1記載の保湿剤。 The humectant according to any one of claims 1 to 3, wherein the polyhydric alcohol of component (B) is one or more selected from glycerin, propanediol, propylene glycol and dipropylene glycol.
PCT/JP2013/069747 2013-07-22 2013-07-22 Moisturizing agent WO2015011750A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
PCT/JP2013/069747 WO2015011750A1 (en) 2013-07-22 2013-07-22 Moisturizing agent
CN201480032571.1A CN105263471B (en) 2013-07-22 2014-07-17 Moisturizer
JP2015528256A JP6382815B2 (en) 2013-07-22 2014-07-17 Moisturizer
PCT/JP2014/069088 WO2015012198A1 (en) 2013-07-22 2014-07-17 Moisturizing agent
TW103124871A TWI636797B (en) 2013-07-22 2014-07-21 Moisturizer
HK16101803.7A HK1213786A1 (en) 2013-07-22 2016-02-18 Moisturizing agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2013/069747 WO2015011750A1 (en) 2013-07-22 2013-07-22 Moisturizing agent

Publications (1)

Publication Number Publication Date
WO2015011750A1 true WO2015011750A1 (en) 2015-01-29

Family

ID=52392836

Family Applications (2)

Application Number Title Priority Date Filing Date
PCT/JP2013/069747 WO2015011750A1 (en) 2013-07-22 2013-07-22 Moisturizing agent
PCT/JP2014/069088 WO2015012198A1 (en) 2013-07-22 2014-07-17 Moisturizing agent

Family Applications After (1)

Application Number Title Priority Date Filing Date
PCT/JP2014/069088 WO2015012198A1 (en) 2013-07-22 2014-07-17 Moisturizing agent

Country Status (5)

Country Link
JP (1) JP6382815B2 (en)
CN (1) CN105263471B (en)
HK (1) HK1213786A1 (en)
TW (1) TWI636797B (en)
WO (2) WO2015011750A1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6644964B2 (en) * 2015-04-17 2020-02-12 クラシエホームプロダクツ株式会社 Cosmetics
CN108186535A (en) * 2018-03-12 2018-06-22 黑龙江军门现代农业发展有限公司 A kind of brown sugar silk mask
KR102271426B1 (en) * 2020-08-27 2021-07-01 백은주 Massage conditioning agent consisting only of water-soluble substances

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000159653A (en) * 1998-11-24 2000-06-13 Nonogawa Shoji Kk Preparation for external use for skin
FR2826576A1 (en) * 2001-06-27 2003-01-03 Soc Extraction Principes Actif Topical compositions containing an extract of Kluyveromyces species yeasts, having an anti-aging effect
JP2008120792A (en) * 2006-10-16 2008-05-29 Hayashibara Biochem Lab Inc Skin and hair cosmetic having moisture retention and hairdressing activity and method for producing the same
JP2012140348A (en) * 2010-12-28 2012-07-26 Maruzen Pharmaceut Co Ltd Anti-inflammatory agent, anti-aging agent, hair growth tonic, and cosmetic

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05221821A (en) * 1992-02-12 1993-08-31 Sakamoto Yakuhin Kogyo Kk Skin-care cosmetic
CN1235559C (en) * 1998-03-11 2006-01-11 株式会社创研 Skin normalizing agents
US20030113357A1 (en) * 2000-05-23 2003-06-19 The Procter & Gamble Company Skin Care Compositions
WO2013005361A1 (en) * 2011-07-01 2013-01-10 パナソニック株式会社 Image capture device

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000159653A (en) * 1998-11-24 2000-06-13 Nonogawa Shoji Kk Preparation for external use for skin
FR2826576A1 (en) * 2001-06-27 2003-01-03 Soc Extraction Principes Actif Topical compositions containing an extract of Kluyveromyces species yeasts, having an anti-aging effect
JP2008120792A (en) * 2006-10-16 2008-05-29 Hayashibara Biochem Lab Inc Skin and hair cosmetic having moisture retention and hairdressing activity and method for producing the same
JP2012140348A (en) * 2010-12-28 2012-07-26 Maruzen Pharmaceut Co Ltd Anti-inflammatory agent, anti-aging agent, hair growth tonic, and cosmetic

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
NIKKO CHEMICALS CO., LTD., SHIN KESHOHIN HANDBOOK, 30 October 2006 (2006-10-30), pages 95 - 101 *

Also Published As

Publication number Publication date
JP6382815B2 (en) 2018-08-29
WO2015012198A1 (en) 2015-01-29
CN105263471B (en) 2018-09-28
HK1213786A1 (en) 2016-07-15
TWI636797B (en) 2018-10-01
TW201507733A (en) 2015-03-01
JPWO2015012198A1 (en) 2017-03-02
CN105263471A (en) 2016-01-20

Similar Documents

Publication Publication Date Title
KR102156898B1 (en) Ingestible cosmetic composition for skin whitening, skin moisturizing, antioxidant, anti-inflammatory, skin barrier strengthening and skin absorption containing the lactic acid fermentation mixture
CN105451751B (en) Composition for removing skin cutin material containing green tea lactobacillus
KR102194315B1 (en) Antioxidant or skin microbiome balance cosmetic composition comprising centella asiatica fermented extract fermented by inoculating lactobacillus rhamnosus strain
KR20180108504A (en) Fermented product of colostrum and a cosmetic composition using the same
CN112402333A (en) Application of red rice fermentation extract in preparation of cosmetics
KR20190091164A (en) Cosmetic Composition for Improving Skin Condition Containing Ginseng Root Fermentation Extract
JP6382815B2 (en) Moisturizer
KR101855207B1 (en) Cosmetic composition containing fermentative extract of terminalia ferdinandiana with increased amount of vitamin c fermented by aureobasidium pullulans
KR102270709B1 (en) Cosmetic composition for skin improvement containing complex ceramide and natural extracts
TW201010741A (en) Cosmetic composition for anti-aging of the skin comprising phaseolus radiatus extract of fermentation-enzyme treatment
JP2016138099A (en) Oil-in-water emulsion composition
JP3184114B2 (en) Moisturizer
KR101953676B1 (en) Cosmetic composition for skin moisturizing containing ultrasonicating extract of harpagophytum procumbens
CN115813774A (en) Water-oil double-layer refined composition with whitening effect and preparation method and application thereof
KR101880470B1 (en) Cosmetic composition comprising organic acid fermentation and natural polymer for moisturizing effect on the skin
CN112842951B (en) Secondary fermented birch juice and its application in skin external composition
JP6407742B2 (en) Liquid cosmetics
TWI701033B (en) Bundling energy enhancer of collagen fiber
KR102100820B1 (en) Rosa centifolia flower petal fermented by aureobasidium pullulans
KR102119622B1 (en) Cosmetic composition comprising the extract of fermented Sorghum Bicolor sprout for skin anti-wrinkle effect and producing method thereof
KR102026366B1 (en) Cosmetic composition comprising whey fermented product of complex probiotics, production methode thereof and functional cosmetic composition comprising the same
JP2005029546A (en) Alpha-glucosidase activation agent
KR102018512B1 (en) Cosmetic composition comprising extract of saliva miltiorrhiza fermented by aureobasidium pullulans
KR101363028B1 (en) A cosmetic composition for the prevention, improvement or treatment of acne vulgaris comprising the mixture of extract of Melissa officinalis, Citrus bergamia, leaves of Mentha arvensis, Eclipta prostrata and Hovenia dulcis Thunb
KR101715194B1 (en) The method for expression and concentration of kojic acid form nuruk

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 13890123

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

NENP Non-entry into the national phase

Ref country code: JP

122 Ep: pct application non-entry in european phase

Ref document number: 13890123

Country of ref document: EP

Kind code of ref document: A1