JP3923970B2 - Deodorant composition - Google Patents
Deodorant composition Download PDFInfo
- Publication number
- JP3923970B2 JP3923970B2 JP2004287962A JP2004287962A JP3923970B2 JP 3923970 B2 JP3923970 B2 JP 3923970B2 JP 2004287962 A JP2004287962 A JP 2004287962A JP 2004287962 A JP2004287962 A JP 2004287962A JP 3923970 B2 JP3923970 B2 JP 3923970B2
- Authority
- JP
- Japan
- Prior art keywords
- extract
- powder
- deodorant
- deodorant composition
- yellowfin
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 239000002781 deodorant agent Substances 0.000 title claims description 39
- 239000000203 mixture Substances 0.000 title claims description 25
- 239000000843 powder Substances 0.000 claims description 32
- 239000000284 extract Substances 0.000 claims description 31
- 241001222097 Xenocypris argentea Species 0.000 claims description 14
- 230000002209 hydrophobic effect Effects 0.000 claims description 12
- 230000001166 anti-perspirative effect Effects 0.000 claims description 11
- 239000003213 antiperspirant Substances 0.000 claims description 11
- 241000196324 Embryophyta Species 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 9
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 8
- 244000111489 Gardenia augusta Species 0.000 claims description 7
- 244000194101 Ginkgo biloba Species 0.000 claims description 6
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- 235000006200 Glycyrrhiza glabra Nutrition 0.000 claims description 5
- 238000000605 extraction Methods 0.000 claims description 5
- 235000001453 Glycyrrhiza echinata Nutrition 0.000 claims description 4
- 235000017382 Glycyrrhiza lepidota Nutrition 0.000 claims description 4
- 239000001569 carbon dioxide Substances 0.000 claims description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 4
- 230000000855 fungicidal effect Effects 0.000 claims description 4
- 239000000417 fungicide Substances 0.000 claims description 4
- 229940010454 licorice Drugs 0.000 claims description 4
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 21
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
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- 239000000395 magnesium oxide Substances 0.000 description 11
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- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 10
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- 239000002537 cosmetic Substances 0.000 description 2
- 230000001877 deodorizing effect Effects 0.000 description 2
- 150000001982 diacylglycerols Chemical class 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
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- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 2
- 229940089456 isopropyl stearate Drugs 0.000 description 2
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- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
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- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000035900 sweating Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- ICUTUKXCWQYESQ-UHFFFAOYSA-N triclocarban Chemical compound C1=CC(Cl)=CC=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 ICUTUKXCWQYESQ-UHFFFAOYSA-N 0.000 description 1
- 229960003500 triclosan Drugs 0.000 description 1
- 238000001262 western blot Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Landscapes
- Cosmetics (AREA)
Description
本発明は、デオドラント効果に優れ、肌上での白残りがなく、しかも制汗作用や感触向上を意図とした粉体の分散安定性が良好なデオドラント組成物に関する。 The present invention relates to a deodorant composition that is excellent in deodorant effect, has no white residue on the skin, and has good powder dispersion stability intended to improve antiperspirant action and feel.
制汗デオドラント剤は、体臭を抑制することを目的として広く使用されているが、未だ十分なデオドラント効果は得られていない。
デオドラント効果を向上させるため、用いる制汗剤の制汗性能を向上させたり(特許文献1)、香料によるマスキング、殺菌剤の大量配合などが試みられている。
Antiperspirant deodorant agents are widely used for the purpose of suppressing body odor, but a sufficient deodorant effect has not yet been obtained.
In order to improve the deodorant effect, attempts have been made to improve the antiperspirant performance of the antiperspirant used (Patent Document 1), masking with a fragrance, and a large amount of a bactericide.
しかしながら、生物学上、発汗を完全に止めることは不可能であるし、マスキングでは効果が持続せず、隠しきれない臭いも存在する。また、殺菌剤の配合は安全性や環境負荷の見地から、少量であるのが望ましい。
更に、粉体を含むデオドラント剤は、適用後に肌に白残りが生じ、外観が損なわれるという問題もあった。
Furthermore, the deodorant agent containing powder also has a problem that a white residue is generated on the skin after application and the appearance is impaired.
本発明の目的は、デオドラント効果に優れ、肌上での粉体の白残りがなく、しかも粉体の分散安定性が良好なデオドラント組成物を提供することにある。 An object of the present invention is to provide a deodorant composition which has an excellent deodorant effect, has no white residue of powder on the skin, and has good dispersion stability of the powder.
本発明者は、特定の植物抽出物と、制汗剤及び/又は殺菌剤とを組み合わせて用いることにより、デオドラント効果に優れ、肌上での白残りがなく、しかも粉体の分散安定性が良好なデオドラント組成物が得られることを見出した。 By using a specific plant extract in combination with an antiperspirant and / or a fungicide, the inventor has excellent deodorant effect, no white residue on the skin, and powder dispersion stability. It has been found that a good deodorant composition can be obtained.
本発明は、(A)キハダ、イチョウ、ムラサキ、カンゾウ及びクチナシから選ばれる植物又はその抽出物から、疎水性溶媒で抽出して得られる疎水性画分、並びに
(B)制汗剤及び/又は殺菌剤
を含有するデオドラント組成物を提供するものである。
The present invention includes (A) a hydrophobic fraction obtained by extraction with a hydrophobic solvent from a plant selected from yellowfin, ginkgo, purple, licorice and gardenia or an extract thereof , and (B) an antiperspirant and / or A deodorant composition containing a bactericide is provided.
本発明のデオドラント組成物は、デオドラント効果に優れ、肌上での粉体の白残りがなく、しかも粉体の分散安定性が良好である。
本発明で用いる植物抽出物のうち、キハダ抽出物は殺菌作用を有することが知られているが(例えば、特開2001-226213号公報、特開2003-113013号公報)、一般的な殺菌剤と比べるとその効果は低い。例えば、黄色ブドウ球菌でのMIC(Minimum Inhibitory Concentration;最小発育阻止濃度)は、一般的な殺菌剤であるイソプロピルメチルフェノールが0.015%であるのに対し、キハダ抽出物は0.15〜2.5%である(臨床と微生物,Vol.26, No.2, p.219(1999))。
本発明で用いる特定の植物抽出物は、皮膚表面における、におい分子のキャリヤータンパク質であるアポリポプロテインDの微生物による分解を抑制する作用を有するものであり、このような作用を有する特定の植物抽出物を、制汗剤又は殺菌剤と組み合わせて用いることにより、アポリポプロテインDの分解抑制効果がより高められ、優れたデオドラント効果が得られるものである。
The deodorant composition of the present invention is excellent in the deodorant effect, has no white residue of the powder on the skin, and has good powder dispersion stability.
Among the plant extracts used in the present invention, yellowfin extract is known to have a bactericidal action (for example, JP 2001-226213 A, JP 2003-113013 A), but a general fungicide. The effect is low compared to. For example, MIC (Minimum Inhibitory Concentration) in Staphylococcus aureus is 0.015% for isopropylmethylphenol, a common fungicide, whereas 0.15-2 for yellowfin extract. 5% (Clinical and Microbiology, Vol. 26, No. 2, p. 219 (1999)).
The specific plant extract used in the present invention has an action of suppressing the degradation of apolipoprotein D, which is a carrier protein of the odor molecule, on the skin surface by microorganisms, and the specific plant extract having such an action Is used in combination with an antiperspirant or bactericidal agent, the effect of inhibiting the degradation of apolipoprotein D is further enhanced, and an excellent deodorant effect can be obtained.
本発明で用いられる成分(A)の原体となる植物は、キハダ、イチョウ、ムラサキ、カンゾウ及びクチナシから選ばれるものである。
これらの植物は、その全草又は葉、根、根茎、果実、種子及び花等の部分を、そのまま又は粉砕して用いることができるが、キハダは樹皮(オウバク)、イチョウは葉、ムラサキは根(シコン)、カンゾウは根、クチナシは実を用いるのが好ましい。
The plant that is the base of the component (A) used in the present invention is selected from yellowfin, ginkgo, purple, licorice and gardenia.
These plants can be used as they are or after pulverizing the whole plant or leaves, roots, rhizomes, fruits, seeds and flowers, but yellowfin is bark, ginkgo is leaf, purple is root. It is preferable to use root for licorice and fruit for gardenia.
本発明において抽出物とは、これらの植物から、適当な溶剤を用いて、常温又は加温下にて抽出するか又はソックスレー抽出器等の抽出器具を用いて抽出することにより得られる各種溶剤抽出液、その希釈液、その濃縮液又はその乾燥末を意味するものである。ここで抽出物は、上記のうち2種以上の植物から得られた混合物であっても良い。 In the present invention, the extract refers to various solvent extractions obtained by extracting from these plants using an appropriate solvent at room temperature or under heating, or using an extraction device such as a Soxhlet extractor. Liquid, its diluted solution, its concentrated solution or its dry powder. Here, the extract may be a mixture obtained from two or more kinds of plants.
抽出に用いる溶剤としては、水;メタノール、エタノール、プロパノール、ブタノール等のアルコール類;プロピレングリコール、ブチレングリコール等の多価アルコール;アセトン、メチルエチルケトン等のケトン類;酢酸メチル、酢酸エチル等のエステル類;テトラヒドロフラン、ジエチルエーテル等の鎖状及び環状エーテル類;ジクロロメタン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類;ヘキサン、シクロヘキサン、石油エーテル等の炭化水素類;ベンゼン、トルエン等の芳香族炭化水素類;平均分子量が180〜1000のポリエチレングリコール;ピリジン;ミリスチン酸イソプロピル、ステアリン酸イソプロピル等のエステル油;オリーブ油、ジアシルグリセロール等の油脂類;超臨界二酸化炭素などが挙げられる。これらを単独で又は組合わせて用いることができる。 Solvents used for extraction include water; alcohols such as methanol, ethanol, propanol and butanol; polyhydric alcohols such as propylene glycol and butylene glycol; ketones such as acetone and methyl ethyl ketone; esters such as methyl acetate and ethyl acetate; Chain and cyclic ethers such as tetrahydrofuran and diethyl ether; Halogenated hydrocarbons such as dichloromethane, chloroform and carbon tetrachloride; Hydrocarbons such as hexane, cyclohexane and petroleum ether; Aromatic hydrocarbons such as benzene and toluene Polyethylene glycol having an average molecular weight of 180 to 1000; pyridine; ester oils such as isopropyl myristate and isopropyl stearate; fats and oils such as olive oil and diacylglycerol; supercritical carbon dioxideThese can be used alone or in combination.
単独で用いる場合はエタノール、アセトン、ヘキサン、油脂類、超臨界二酸化炭素等が好ましい。組合わせて用いる場合には、水−アルコール混液、特に水−エタノール混液が好ましく、エタノール含有量は50v/v%以上、特に80v/v%以上、更に95v/v%が好ましい。 When used alone, ethanol, acetone, hexane, fats and oils, supercritical carbon dioxide and the like are preferable. When used in combination, a water-alcohol mixture, particularly a water-ethanol mixture is preferred, and the ethanol content is preferably 50 v / v% or more, particularly 80 v / v% or more, and more preferably 95 v / v%.
抽出条件は、使用する溶媒によっても異なるが、例えば、水−エタノール混液により抽出する場合、植物10gに対して70〜150mLの溶剤を用い、15〜35℃、好ましくは20〜25℃の温度で、30時間〜10日間、特に5〜8日間抽出するのが好ましい。 Extraction conditions vary depending on the solvent to be used. For example, when extracting with a water-ethanol mixed solution, 70 to 150 mL of solvent is used for 10 g of plant, and the temperature is 15 to 35 ° C, preferably 20 to 25 ° C. 30 hours to 10 days, particularly 5 to 8 days.
本発明においては、前記植物の抽出物の疎水性画分、すなわち、前記植物又はその抽出物から、疎水性溶媒で抽出して得られる画分を用いるのが好ましい。ここで用いられる疎水性溶媒としては、例えば、酢酸メチル、酢酸エチル等のエステル類;ジエチルエーテル等のエーテル類;ジクロロメタン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類;ヘキサン、シクロヘキサン、石油エーテル、スクワラン等の炭化水素類;ベンゼン、トルエン等の芳香族炭化水素類;超臨界二酸化炭素;ミリスチン酸イソプロピル、ステアリン酸イソプロピル等のエステル油;オリーブ油、ジアシルグリセロール等の油脂類;シリコーン油などが挙げられる。これらを単独で又は組合わせて用いることができる。なかでも、超臨界二酸化炭素又はヘキサンを用いるのが好ましい。 In the present invention, it is preferable to use a hydrophobic fraction of the plant extract, that is, a fraction obtained by extracting the plant or the extract thereof with a hydrophobic solvent. Examples of the hydrophobic solvent used here include esters such as methyl acetate and ethyl acetate; ethers such as diethyl ether; halogenated hydrocarbons such as dichloromethane, chloroform and carbon tetrachloride; hexane, cyclohexane and petroleum ether Hydrocarbons such as squalane; aromatic hydrocarbons such as benzene and toluene; supercritical carbon dioxide; ester oils such as isopropyl myristate and isopropyl stearate; fats and oils such as olive oil and diacylglycerol; and silicone oils It is done. These can be used alone or in combination. Among these, it is preferable to use supercritical carbon dioxide or hexane.
また、液々分配等の技術により、上記抽出物から不活性な爽雑物を除去して用いることもでき、本発明においてはこのようなものを用いるのが好ましい。これらは、必要により公知の方法で脱臭、脱色等の処理を施してから用いてもよい。 In addition, it is possible to remove inactive contaminants from the extract by a technique such as liquid-liquid distribution, and it is preferable to use such an extract in the present invention. These may be used after performing treatments such as deodorization and decolorization by a known method if necessary.
これらの抽出物は、そのまま用いることもできるが、当該抽出物を希釈調製して、又は濃縮若しくは凍結乾燥により粉末又はペースト状に調製して用いることもできる。 These extracts can be used as they are, but can also be used by diluting the extract or preparing it in a powder or paste form by concentration or lyophilization.
成分(A)は、固形分換算で、全組成物中に0.0001〜5質量%、特に0.0005〜2質量%含有するのが好ましい。 Component (A) is preferably contained in the total composition in an amount of 0.0001 to 5% by mass, particularly 0.0005 to 2% by mass in terms of solid content.
本発明で用いる成分(B)のうち、制汗剤としては、例えばアルミニウムクロロハイドレート、アルミニウムジルコニウムクロロハイドレート、塩化アルミニウム、硫酸アルミニウム、塩基性臭化アルミニウム、アルミニウムフェノールスルホン酸、塩基性ヨウ化アルミニウム等が挙げられ、全組成中に0.1〜30%、特に1〜25%質量%含有するのが、肌感触と効果的な制汗効果を得られるので好ましい。
また、殺菌剤としては、3,4,4−トリクロロカルバアニリド、トリクロサン、塩化ベンザルコニウム、塩化ベンゼトニウム、塩化アルキルトリメチルアンモニウム、レゾルシン、フェノール、ソルビン酸、サリチル酸、ヘキサクロロフェン、イソプロピルメチルフェノール等が挙げられ、全組成中に0.0001〜1質量%、特に0.0005〜0.5質量%含有するのが安全性と菌の生育を効果的に抑制するため好ましい。
Among the component (B) used in the present invention, examples of the antiperspirant include aluminum chlorohydrate, aluminum zirconium chlorohydrate, aluminum chloride, aluminum sulfate, basic aluminum bromide, aluminum phenolsulfonic acid, and basic iodide. Aluminum etc. are mentioned, and it is preferable to contain 0.1 to 30%, especially 1 to 25% by mass in the total composition, since the skin feel and the effective antiperspirant effect can be obtained.
Examples of bactericides include 3,4,4-trichlorocarbanilide, triclosan, benzalkonium chloride, benzethonium chloride, alkyltrimethylammonium chloride, resorcin, phenol, sorbic acid, salicylic acid, hexachlorophene, isopropylmethylphenol and the like. It is preferable to contain 0.0001 to 1% by mass, particularly 0.0005 to 0.5% by mass in the total composition, in order to effectively suppress the safety and growth of bacteria.
成分(B)は、1種以上を用いることができ、制汗剤と殺菌剤を組み合わせて用いることもできる。 As the component (B), one or more kinds can be used, and an antiperspirant and a disinfectant can be used in combination.
本発明のデオドラント組成物は、更に(C)消臭粉体を含有することができる。
消臭粉体としては、キトサン微粒子、両性の多孔性微粒子、ゼオライト、抗菌性ゼオライト、多孔質シリカ、酸化亜鉛、酸化マグネシウム等が挙げられる。
The deodorant composition of the present invention can further contain (C) a deodorant powder.
Examples of the deodorant powder include chitosan fine particles, amphoteric porous fine particles, zeolite, antibacterial zeolite, porous silica, zinc oxide, and magnesium oxide.
キトサン微粒子としては、平均粒径0.01〜50μmのものが好ましく、例えば特開平7-304643号公報に記載のもの等を用いることができる。
両性の多孔性微粒子としては、平均粒径0.01〜50μmのものが好ましく、例えば特開平7-316203号公報に記載のもの等を用いることができる。
As the chitosan fine particles, those having an average particle diameter of 0.01 to 50 μm are preferable. For example, those described in JP-A-7-304643 can be used.
As the amphoteric porous fine particles, those having an average particle diameter of 0.01 to 50 μm are preferable. For example, those described in JP-A-7-316203 can be used.
抗菌性ゼオライトとしては、ゼオライトのイオン交換可能な部分に抗菌性金属イオンを保持したものを用いることができる。抗菌性金属イオンとしては、銀、銅、亜鉛等のイオンが好ましく、特に、銀担持ゼオライトが好ましい。このような抗菌性ゼオライトは、例えば特開平8-26955号公報に記載の方法により製造することができる。 As the antibacterial zeolite, one holding an antibacterial metal ion in an ion-exchangeable part of the zeolite can be used. As the antibacterial metal ion, ions such as silver, copper, and zinc are preferable, and silver-supported zeolite is particularly preferable. Such antibacterial zeolite can be produced, for example, by the method described in JP-A-8-26955.
酸化マグネシウムとしては、通常の酸化マグネシウム粉体のほか、消臭効果を高めた酸化マグネシウム、例えば、比表面積が120〜300m2/gで、細孔容積が0.8〜1.5mL/gである酸化マグネシウム粉体(特開2001-187721号公報)等を用いることもできる。 As magnesium oxide, in addition to normal magnesium oxide powder, magnesium oxide with enhanced deodorizing effect, for example, specific surface area is 120 to 300 m 2 / g, and pore volume is 0.8 to 1.5 mL / g. A certain magnesium oxide powder (Japanese Patent Laid-Open No. 2001-187721) or the like can also be used.
また、これらの粉体を、ナイロン、ポリエチレン、シリカ等に表面被覆処理したり、複合化して用いることもできる。例えば、ナイロン、ポリエチレン、ポリプロピレン等の合成樹脂と、酸化亜鉛、酸化マグネシウム、酸化カルシウム等の金属酸化物からなる複合粉体(特開昭61-217139号公報)、亜鉛、銀、銅等の金属又はその酸化物とケイ酸塩の複合体(特開2000-159602号公報)、化粧料用粉体と水酸化アルミニウムを含有する複合粉体(特開2002-146238号公報)、非晶質シリカ、非晶質シリカ−アルミナ又は非晶質アルミノ珪酸塩を、水酸化マグネシウム、ケイ酸マグネシウム、酸化マグネシウム等のマグネシウム化合物で被覆した粒子(特開平7-138140号公報)、無水ケイ酸粒子中に酸化マグネシウムを担持させた粉体(特開平10-338621号公報)、二酸化ケイ素と酸化マグネシウムを複合化した多孔質粉体(特開2003-73249号公報)などを用いることができる。 Further, these powders can be used after being surface-coated on nylon, polyethylene, silica or the like or combined. For example, composite powder made of synthetic resin such as nylon, polyethylene, polypropylene and metal oxide such as zinc oxide, magnesium oxide, calcium oxide (Japanese Patent Laid-Open No. 61-217139), metal such as zinc, silver, copper Or a composite of oxide and silicate thereof (Japanese Patent Laid-Open No. 2000-159602), composite powder containing cosmetic powder and aluminum hydroxide (Japanese Patent Laid-Open No. 2002-146238), amorphous silica In the particles of amorphous silica-alumina or amorphous aluminosilicate coated with a magnesium compound such as magnesium hydroxide, magnesium silicate, magnesium oxide (JP-A-7-138140), A powder supporting magnesium oxide (Japanese Patent Laid-Open No. 10-338621), a porous powder composited of silicon dioxide and magnesium oxide (Japanese Patent Laid-Open No. 2003-73249), and the like can be used.
消臭粉体としては、無機粉体が好ましく、特にゼオライト、抗菌性ゼオライト、多孔質シリカ、酸化亜鉛、酸化マグネシウムが好ましい。 As the deodorant powder, inorganic powder is preferable, and zeolite, antibacterial zeolite, porous silica, zinc oxide, and magnesium oxide are particularly preferable.
成分(C)の消臭粉体は、1種以上を用いることができ、全組成中に0.1〜10質量%、特に0.5〜5質量%含有するのが、消臭効果と肌感触に優れるので好ましい。 One or more deodorant powders of the component (C) can be used, and 0.1 to 10% by mass, particularly 0.5 to 5% by mass is contained in the total composition, and the deodorizing effect and the skin. It is preferable because it is excellent in touch.
本発明のデオドラント組成物には、前記成分以外に、通常の化粧料等に用いられる成分、例えば油性成分、水、各種界面活性剤、高分子化合物、湿潤剤、防腐剤、酸化防止剤、薬効成分、香料、粉体、噴射剤等を含有させることができる。 In addition to the above components, the deodorant composition of the present invention includes components used in normal cosmetics, such as oil components, water, various surfactants, polymer compounds, wetting agents, preservatives, antioxidants, medicinal effects. Components, fragrances, powders, propellants and the like can be included.
本発明のデオドラント組成物は、例えばエアゾールスプレー、ポンプスプレー、ロールオン、パウダー、スティック、クリーム等の形態にすることができる。 The deodorant composition of the present invention can be in the form of, for example, aerosol spray, pump spray, roll-on, powder, stick, cream and the like.
製造例1(キハダ抽出物の調製)
キハダの樹皮10gに95v/v%エタノール水溶液100mLを加え、室温で7日間抽出後、濾過して抽出液を得た(収量:87mL、蒸発残分:0.72w/v%)。
Production Example 1 (Preparation of yellowfin extract)
To 10 g of yellowfin bark, 100 mL of a 95 v / v% aqueous ethanol solution was added, extracted at room temperature for 7 days, and filtered to obtain an extract (yield: 87 mL, evaporation residue: 0.72 w / v%).
製造例2(キハダエキス疎水性画分の調製)
キハダの樹皮10gに95v/v%エタノール水溶液100mLを加え、室温で7日間抽出後、濾過して抽出液を得た。この抽出液を減圧濃縮後、更にヘキサン100mLで抽出し、濾過して抽出液を得た。これを減圧濃縮し、さらに減圧乾燥して、キハダエキス疎水性画分を得た(収量:0.28g)。
Production Example 2 (Preparation of yellowfin extract hydrophobic fraction)
To 10 g of yellowfin bark, 100 mL of a 95 v / v% aqueous ethanol solution was added, extracted at room temperature for 7 days, and then filtered to obtain an extract. The extract was concentrated under reduced pressure, further extracted with 100 mL of hexane, and filtered to obtain an extract. This was concentrated under reduced pressure and further dried under reduced pressure to obtain a yellowfin extract hydrophobic fraction (yield: 0.28 g).
製造例3(イチョウ抽出物の調製)
イチョウの葉10gに95v/v%エタノール水溶液100mLを加え、室温で7日間抽出後、濾過して抽出液を得た(収量:85mL、蒸発残分:1.59w/v%)。
Production Example 3 (Preparation of Ginkgo biloba extract)
100 g of a 95 v / v% ethanol aqueous solution was added to 10 g of ginkgo biloba, extracted at room temperature for 7 days, and then filtered to obtain an extract (yield: 85 mL, evaporation residue: 1.59 w / v%).
製造例4(ムラサキ抽出物の調製)
ムラサキの根10gにヘキサン100mLを加え、室温で7日間抽出後、濾過して抽出液を得た(収量:84mL、蒸発残分:0.12w/v%)。
Production Example 4 (Preparation of Murasaki Extract)
Hexane root (10 g) was added with hexane (100 mL), extracted at room temperature for 7 days, and filtered to obtain an extract (yield: 84 mL, evaporation residue: 0.12 w / v%).
製造例5(カンゾウ抽出物の調製)
カンゾウの根10gに50v/v%エタノール水溶液100mLを加え、室温で7日間抽出後、濾過して抽出液を得た(収量:78mL、蒸発残分:3.07w/v%)。
Production Example 5 (Preparation of licorice extract)
100 g of 50 v / v% aqueous ethanol solution was added to 10 g of licorice roots, extracted at room temperature for 7 days, and filtered to obtain an extract (yield: 78 mL, evaporation residue: 3.07 w / v%).
製造例6(クチナシ抽出物の調製)
クチナシの実10gに95v/v%エタノール水溶液100mLを加え、室温で7日間抽出後、濾過して抽出液を得た(収量:93mL、蒸発残分:1.69w/v%)。
Production Example 6 (Preparation of gardenia extract)
100 g of 95 v / v% ethanol aqueous solution was added to 10 g of gardenia seeds, extracted at room temperature for 7 days, and filtered to obtain an extract (yield: 93 mL, evaporation residue: 1.69 w / v%).
試験例1(アポリポプロテインD分解抑制作用)
(1)濃縮汗の調製:
アポクリン臭を有する男性8名の脇の下を、蒸留水1.5mLを含ませた脱脂綿で拭き取る操作を1日1回、3日間行った。これらの脱脂綿を絞って回収した液(57.5mL)を、孔径0.45μmのフィルターでろ過した後、ミリポア社の遠心濾過膜「セントリプレップYM−10」で濃縮をし、再度蒸留水を添加して同様にセントリプレップYM−10で濃縮し、低分子成分を除去した。これを濃縮汗とした。
Test Example 1 (Apolipoprotein D degradation inhibitory action)
(1) Preparation of concentrated sweat:
The operation of wiping the armpits of 8 men with apocrine odor with absorbent cotton containing 1.5 mL of distilled water was performed once a day for 3 days. The liquid (57.5 mL) collected by squeezing these absorbent cottons is filtered through a filter with a pore size of 0.45 μm, concentrated with a Millipore centrifugal filter membrane “Centreprep YM-10”, and distilled water is added again In the same manner, it was concentrated with Centriprep YM-10 to remove low molecular components. This was concentrated sweat.
(2)上記方法(1)によって調製した濃縮汗0.04mLに、0.03mLの100mMトリス−HClバッファー、0.02mLの蒸留水及び0.01mLの各植物抽出物(製造例1及び3〜6)を添加した。これに、pH7.2、20mMトリス−HClバッファーで洗浄(3回)したBrevibacterium epiderumidisを、最終菌体量が約108cfu/mLになるように接種し、37℃、24時間インキュベートした後、抗体染色を行った。菌体処理濃縮汗のSDSポリアクリルアミド電気泳動(SDS−PAGE)のゲルとしては、レディゲルJ(分離ゲル濃度15%、バイオラッド社)を用いた。抗体染色はSDS−PAGEで分離したタンパク質をゲルからPVDFフィルター(Immobilonトランスファー膜、ミリポア社)上へ電気的に転写後、一次抗体に抗アポリポプロテインDモノクローナルマウス抗体(RDI社)、二次抗体にHRP標識の抗マウスIg抗体(アマシャム ファルマシア バイオテク社)を用い、ECL Plusウェスタンブロッティング検出システム(アマシャム ファルマシア バイオテク社)によって、アポリポプロテインDを検出後、画像処理を行い、アポリポプロテインDの残存率、即ち、(サンプルのアポリポプロテインD量/未処理汗中のアポリポプロテインD量)×100を算出した。 (2) To 0.04 mL of concentrated sweat prepared by the above method (1), 0.03 mL of 100 mM Tris-HCl buffer, 0.02 mL of distilled water and 0.01 mL of each plant extract (Production Examples 1 and 3) 6) was added. This was inoculated with Brevibacterium epiderumidis washed 3 times with pH 7.2, 20 mM Tris-HCl buffer so that the final cell mass was about 10 8 cfu / mL, and incubated at 37 ° C. for 24 hours. Antibody staining was performed. As a gel of SDS polyacrylamide electrophoresis (SDS-PAGE) of bacterial cell-treated concentrated sweat, Ready Gel J (separated gel concentration: 15%, Bio-Rad) was used. For antibody staining, the protein separated by SDS-PAGE is electrically transferred from the gel onto a PVDF filter (Immobilon transfer membrane, Millipore), then the primary antibody is anti-apolipoprotein D monoclonal mouse antibody (RDI), and the secondary antibody is An apolipoprotein D was detected by an ECL Plus Western blotting detection system (Amersham Pharmacia Biotech) using an anti-mouse Ig antibody labeled with HRP (Amersham Pharmacia Biotech), and image processing was performed. , (Apolipoprotein D amount of sample / Apolipoprotein D amount in untreated sweat) × 100 was calculated.
その結果、アポリポプロテインDの残存率は、植物抽出物を添加しない場合に51%であったのに対し、キハダ抽出物85%、イチョウ抽出物81%、ムラサキ抽出物82%、カンゾウ抽出物72%、クチナシ抽出物80%であった。
濃縮汗をBrevibacterium epiderumidis処理することによって、濃縮汗中のアポリポプロテインDが分解され減少するのに対して、特定の植物抽出物を添加することにより、アポリポプロテインDの分解が抑制された。
As a result, the residual rate of apolipoprotein D was 51% when no plant extract was added, whereas it was 85% yellowfin extract, 81% ginkgo extract, 82% purple extract, and licorice extract 72. %, Gardenia extract 80%.
By treating the concentrated sweat with Brevibacterium epiderumidis , apolipoprotein D in the concentrated sweat was decomposed and decreased, whereas the addition of a specific plant extract suppressed the degradation of apolipoprotein D.
実施例1〜3、比較例1〜2
表1に示す組成のパウダースプレーを製造し、デオドラント効果、粉体の分散安定性及び肌上での白残りについて評価した。結果を表1に併せて示す。
Examples 1-3 , Comparative Examples 1-2
A powder spray having the composition shown in Table 1 was produced, and the deodorant effect, the dispersion stability of the powder, and the white residue on the skin were evaluated. The results are also shown in Table 1.
(製造方法)
各植物抽出物、ミリスチン酸イソプロピル、デカメチルシクロペンタシロキサンを均一に混合した後、その溶液と粉体(アルミニウムクロロハイドレート、ゼオライト)とをエアゾール容器に充填し、クリンチした後、LPGを圧入した。
(Production method)
After each plant extract, isopropyl myristate, and decamethylcyclopentasiloxane were uniformly mixed, the solution and powder (aluminum chlorohydrate, zeolite) were filled into an aerosol container, clinched, and then LPG was injected. .
(評価方法)
(1)肌上での白残り及びデオドラント効果:
各パウダースプレーについて、強い腋臭を有するパネラー10名の腋の下に剤を0.5g噴霧し、噴霧後の肌上での白残りを、以下の基準に従い官能評価した。また、8時間後において、デオドラント効果を以下の基準に従い評価した。
(Evaluation methods)
(1) White residue and deodorant effect on skin:
For each powder spray, 0.5 g of the agent was sprayed under the cocoons of 10 panelists having a strong odor, and the white residue on the skin after spraying was subjected to sensory evaluation according to the following criteria. Further, after 8 hours, the deodorant effect was evaluated according to the following criteria.
(肌上での白残り)
スコア4:白くならない。
スコア3:あまり白くならない。
スコア2:やや白くなる。
スコア1:白くなる。
(White residue on skin)
Score 4: Does not turn white.
Score 3: Not very white.
Score 2: Slightly white.
Score 1: turns white.
(デオドラント効果)
スコア4:非常にデオドラント効果が高い。
スコア3:デオドラント効果が高い。
スコア2:デオドラント効果がやや低い。
スコア1:デオドラント効果が低い。
(Deodorant effect)
Score 4: Very high deodorant effect.
Score 3: Deodorant effect is high.
Score 2: Deodorant effect is slightly low.
Score 1: Deodorant effect is low.
平均スコアを求め、以下の基準により判定した。
◎:平均スコア3.5〜4.0。
○:平均スコア2.5〜3.4。
△:平均スコア1.5〜2.4。
×:平均スコア1.0〜1.4。
The average score was determined and judged according to the following criteria.
A: Average score of 3.5 to 4.0.
A: Average score of 2.5 to 3.4.
(Triangle | delta): Average score 1.5-2.4.
X: Average score of 1.0 to 1.4.
(2)粉体の分散安定性:
各パウダースプレーについて、剤をガラス瓶に充填し、室温で容器を振った時の粉体の分散状態を、評価専門パネラー5名により、以下の基準で目視評価した。平均スコアを求め、(1)と同様にして判定した。
スコア4:非常に良い。
スコア3:良い。
スコア2:やや悪い。
スコア1:悪い。
(2) Dispersion stability of powder:
About each powder spray, the agent was filled in the glass bottle, and the dispersion state of the powder when the container was shaken at room temperature was visually evaluated by the following 5 evaluation panelists based on the following criteria. An average score was determined and determined in the same manner as (1).
Score 4: very good.
Score 3: Good.
Score 2: Slightly bad.
Score 1: bad.
実施例4(パウダースプレー)
以下に示す組成のパウダースプレーを常法により製造した。
(成分)
キハダエキス疎水性画分(製造例2) 0.005(質量%)
アルミニウムクロロハイドレート
(ロクロンP、Hoechst AG社製) 1.50
酸化マグネシウム被覆シリカ 1.00
パルミチン酸イソプロピル 2.50
ポリオキシエチレン・メチルポリシロキサン共重合体
(KF−6015、信越化学社製) 0.02
イソステアリルアルコール 0.50
オレイン酸 0.10
香料 0.30
デカメチルシクロペンタシロキサン
(SH−245、東レ・ダウコーニング・シリコーン社製) 2.075
LPG 92.00
Example 4 (powder spray)
A powder spray having the following composition was produced by a conventional method.
(component)
Yellowfin extract hydrophobic fraction (Production Example 2) 0.005 (mass%)
Aluminum chlorohydrate (Rocron P, manufactured by Hoechst AG) 1.50
Magnesium oxide coated silica 1.00
Isopropyl palmitate 2.50
Polyoxyethylene / methylpolysiloxane copolymer (KF-6015, manufactured by Shin-Etsu Chemical Co., Ltd.) 0.02
Isostearyl alcohol 0.50
Oleic acid 0.10
Fragrance 0.30
Decamethylcyclopentasiloxane (SH-245, manufactured by Toray Dow Corning Silicone) 2.075
LPG 92.00
実施例5(ポンプスプレー)
以下に示す組成のポンプスプレーを常法により製造した。
(成分)
ムラサキ抽出物(製造例4) 0.20(質量%)
アルミニウムクロロハイドレート
(REACH 501 solution、REHEIS社製) 2.00
イソプロピルメチルフェノール 0.20
多孔質シリカ 2.00
ポリオキシエチレン(20EO)ヤシ油脂肪酸ソルビタン
(レオドールTW−L120、花王社製) 0.20
ミリスチン酸イソプロピル 0.10
酸化亜鉛被覆ナイロン 0.20
リノール酸 0.01
香料 0.20
精製水 7.89
エタノール 87.00
Example 5 (pump spray)
A pump spray having the following composition was produced by a conventional method.
(component)
Purple extract (Production Example 4) 0.20 (% by mass)
Aluminum chlorohydrate (REACH 501 solution, manufactured by REHEIS) 2.00
Isopropylmethylphenol 0.20
Porous silica 2.00
Polyoxyethylene (20EO) coconut oil fatty acid sorbitan (Leodol TW-L120, manufactured by Kao Corporation) 0.20
Isopropyl myristate 0.10
Zinc oxide coated nylon 0.20
Linoleic acid 0.01
Fragrance 0.20
Purified water 7.89
Ethanol 87.00
実施例4〜5で得られたデオドラント組成物はいずれも、デオドラント効果に優れ、肌上での白残りがなく、しかも粉体の安定性も良好であった。 All of the deodorant compositions obtained in Examples 4 to 5 were excellent in the deodorant effect, had no white residue on the skin, and had good powder stability.
Claims (5)
(B)制汗剤及び/又は殺菌剤
を含有するデオドラント組成物。 (A) Hydrophobic fraction obtained by extraction with a hydrophobic solvent from a plant selected from yellowfin, ginkgo, purple, licorice and gardenia or an extract thereof , and (B) containing an antiperspirant and / or a fungicide Deodorant composition.
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