JP2608745B2 - Whitening cosmetics - Google Patents

Whitening cosmetics

Info

Publication number
JP2608745B2
JP2608745B2 JP63011583A JP1158388A JP2608745B2 JP 2608745 B2 JP2608745 B2 JP 2608745B2 JP 63011583 A JP63011583 A JP 63011583A JP 1158388 A JP1158388 A JP 1158388A JP 2608745 B2 JP2608745 B2 JP 2608745B2
Authority
JP
Japan
Prior art keywords
acid
extract
pigmentation
photosensitizer
cosmetic
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
Application number
JP63011583A
Other languages
Japanese (ja)
Other versions
JPH01186809A (en
Inventor
秀哉 安藤
晃 橋本
満章 清水
久豊 加藤
祥次 小笹
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sunstar Inc
Original Assignee
Sunstar Inc
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 Sunstar Inc filed Critical Sunstar Inc
Priority to JP63011583A priority Critical patent/JP2608745B2/en
Publication of JPH01186809A publication Critical patent/JPH01186809A/en
Application granted granted Critical
Publication of JP2608745B2 publication Critical patent/JP2608745B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/37Esters of carboxylic acids
    • 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
    • A61K8/67Vitamins
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/02Preparations for care of the skin for chemically bleaching or whitening the skin

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、紫外線による皮膚の黒化あるいはシミ、ソ
バカスなどの皮膚色素沈着の淡色化、もしくは予防を行
う美白化粧料に関する。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a whitening cosmetic which darkens skin by ultraviolet rays or lightens or prevents skin pigmentation such as spots and freckles.

従来の技術および問題点 従来、美白化粧料組成物としてはビタミンCおよびそ
の誘導体、あるいは還元剤、胎盤エキスなどのチロジナ
ーゼ活性阻害剤を配合したものが知られている。しかし
ながら、これら従来の美白化粧料は培養細胞によるin v
itroの実験ではメラニン産生抑制作用などを示すもの
の、実際に皮膚に適用した場合、充分な色素沈着の予防
もしくは淡色化などの効果は得られていない。
2. Description of the Related Art Conventionally, as a whitening cosmetic composition, a composition containing vitamin C and a derivative thereof, or a tyrosinase activity inhibitor such as a reducing agent or placenta extract is known. However, these conventional whitening cosmetics are in v
Although itroin exhibits an inhibitory effect on melanin production in the experiment of itro, when applied to the skin actually, no effect such as sufficient prevention of pigmentation or lightening is obtained.

本発明は実際に皮膚に適用した場合、副作用がなく優
れた美白効果を奏しうる化粧料を提供することを目的と
する。
An object of the present invention is to provide a cosmetic that can exhibit an excellent whitening effect without side effects when actually applied to the skin.

問題点を解決するための手段 本発明者らは、前記目的を達成すべく鋭意研究を重ね
た結果、特定の脂肪酸またはその誘導体に抗炎症剤を組
み合わせることにより皮膚の色素沈着の消失、もしくは
予防に優れた相乗的な効果があらわれることを見いだ
し、本発明を完成するに至った。
Means for Solving the Problems The present inventors have conducted intensive studies to achieve the above object, and as a result, disappearance or prevention of skin pigmentation by combining an anti-inflammatory agent with a specific fatty acid or a derivative thereof. The present inventors have found that an excellent synergistic effect appears, and have completed the present invention.

すなわち本発明は、 (a)炭素数18〜22かつ分子構造中の不飽和結合数が2
以上の遊離脂肪酸、その塩、あるいは一価または二価ア
ルコールとのエステルからなる群より選ばれた1種また
は2種以上の化合物、および (b)イプシロンアミノカプロン酸、グリチルレチン
酸、グリチルリチン酸、その塩、およびその誘導体、感
光素301号、感光素401号、塩酸ジフェンヒドラミン、水
溶性アズレン、アデノシン一リン酸、カラミン、紫根エ
キス、当帰エキス、ヨモギエキス並びにワレモコウエキ
スから選ばれる1種または2種以上 を配合したことを特徴とする美白化粧料を提供するもの
である。
That is, the present invention provides: (a) a compound having 18 to 22 carbon atoms and 2 unsaturated bonds in the molecular structure;
One or more compounds selected from the group consisting of the above free fatty acids, salts thereof, and esters with monohydric or dihydric alcohols, and (b) epsilon aminocaproic acid, glycyrrhetinic acid, glycyrrhizic acid, and salts thereof , And derivatives thereof, one or more selected from photosensitizer 301, photosensitizer 401, diphenhydramine hydrochloride, water-soluble azulene, adenosine monophosphate, calamine, purple root extract, Toki extract, mugwort extract and warmoko extract The present invention provides a skin-whitening cosmetic characterized by incorporating a whitening cosmetic.

本発明組成物に配合されるリノール酸、γ−リノレン
酸など炭素数18〜22を有し、かつ分子構造中の不飽和結
合数が2以上の脂肪酸は、植物油脂および動物油脂に含
まれている。しかし、これら脂肪酸は遊離の状態で存在
することは少なく、そのほとんどはトリグリセリドの状
態で存在する。このようなトリグリセリドは、遊離の脂
肪酸もしくはそのアルキルエステルのごとく動物試験等
において優れた色素沈着淡色化作用は認められない。ま
た、パルミチン酸、ステアリン酸などの飽和脂肪酸にあ
っても同様に色素沈着抑制効果は認められず、場合によ
っては逆にメラニン産生を亢進する。かかる飽和脂肪酸
は、植物油脂および動物油脂に多量にふくまれているた
め、本発明化粧料におけるリノール酸などの配合にあた
っては精製したものを用いることが好ましい。
Fatty acids having 18 to 22 carbon atoms, such as linoleic acid and γ-linolenic acid, which are blended in the composition of the present invention, and having an unsaturated bond number of 2 or more in the molecular structure are contained in vegetable oils and fats. I have. However, these fatty acids rarely exist in a free state, and most of them exist in a triglyceride state. Such a triglyceride does not exhibit an excellent pigmentation and lightening effect in animal tests and the like, as in the case of a free fatty acid or an alkyl ester thereof. Similarly, the effect of inhibiting the pigmentation is not observed even with saturated fatty acids such as palmitic acid and stearic acid, and in some cases, the production of melanin is enhanced. Since such saturated fatty acids are contained in a large amount in vegetable oils and fats and oils, it is preferable to use purified fatty acids when blending linoleic acid in the cosmetic of the present invention.

本発明の美白化粧料に配合される炭素数18〜22かつ分
子構造中の不飽和結合数が2以上の遊離脂肪酸の代表的
なものとしては、リノール酸、リノエライジン酸、α−
リノレン酸、γ−リノレン酸、ジホモ−γ−リノレン
酸、アラキドン酸、エイコサペンタエン酸などが挙げら
れ、これらの1種または2種以上が用いられる。
Representative examples of the free fatty acid having 18 to 22 carbon atoms and having 2 or more unsaturated bonds in the molecular structure to be incorporated in the whitening cosmetic composition of the present invention include linoleic acid, linoleic acid, α-
Examples thereof include linolenic acid, γ-linolenic acid, dihomo-γ-linolenic acid, arachidonic acid, and eicosapentaenoic acid. One or more of these are used.

また、これら遊離脂肪酸の塩としては、ナトリウム
塩、カリウム塩などの金属塩、アルギニン塩、リジン塩
などのアミノ酸塩、トリエタノールアミン塩、モノエタ
ノールアミン塩等のアミン塩などが挙げられる。
Examples of the salts of these free fatty acids include metal salts such as sodium salt and potassium salt, amino acid salts such as arginine salt and lysine salt, and amine salts such as triethanolamine salt and monoethanolamine salt.

さらに、前記遊離脂肪酸のアルキルエステルとして
は、メタノール、エタノール、イソプロピルアルコール
などの一価アルコールとのエステル、エチレングリコー
ル、プロピレングリコール、1,3−ブチレングリコール
などの二価のアルコールとのエステルなどが挙げられ
る。
Further, examples of the alkyl ester of the free fatty acid include an ester with a monohydric alcohol such as methanol, ethanol and isopropyl alcohol, and an ester with a dihydric alcohol such as ethylene glycol, propylene glycol and 1,3-butylene glycol. Can be

これら遊離脂肪酸、塩、またはエステルの化粧料中に
おける配合量は、0.1〜10重量%であるのが好ましい。
かかる配合量が0.1重量%未満であると、色素沈着の抑
制効果がなく、一方、10重量%を越えると、刺激性が強
くなり、使用上好ましくない。
The amount of these free fatty acids, salts or esters in cosmetics is preferably 0.1 to 10% by weight.
When the amount is less than 0.1% by weight, the effect of suppressing pigmentation is not obtained. On the other hand, when the amount exceeds 10% by weight, irritation becomes strong, which is not preferable in use.

一方、本発明組成物に配合される抗炎症剤は、一般に
医薬品、化粧品等に抗炎症作用を有する薬剤として配合
されているものであるが、例えば、イプシロンアミノカ
プロン酸、グリチルレチン酸、グリチルリチン酸、その
塩、およびその誘導体、感光素301号、感光素401号、塩
酸ジフェンヒドラミン、水溶液アズレン(1,4−ジメチ
ル−7−イソプロピルアズレン−3−スルホン酸ナトリ
ウム)、アデノシン一リン酸、カラミン(酸化亜鉛)、
紫根エキス、当帰エキス、ヨモギエキス、ワレモコウエ
キスなどが挙げられ、これらの1種または2種以上が用
いられる。
On the other hand, the anti-inflammatory agent blended in the composition of the present invention is generally formulated as a drug having an anti-inflammatory effect in pharmaceuticals, cosmetics, etc., for example, epsilon aminocaproic acid, glycyrrhetinic acid, glycyrrhizic acid, Salts and derivatives thereof, Photosensitizer 301, Photosensitizer 401, diphenhydramine hydrochloride, aqueous azulene (sodium 1,4-dimethyl-7-isopropylazulene-3-sulfonate), adenosine monophosphate, calamine (zinc oxide) ,
A purple root extract, a Toki extract, a mugwort extract, a valerian extract and the like can be mentioned, and one or more of these are used.

これら抗炎症剤の化粧料組成物中における配合量は0.
01〜5.0重量%であるので好ましい。
The amount of these anti-inflammatory agents in the cosmetic composition is 0.
It is preferable because it is 01 to 5.0% by weight.

なお、従来かかる抗炎症剤が他の活性成分と組み合わ
されて皮膚に対し相乗的な美白効果を示すことについて
は知られていない。
Heretofore, it has not been known that such anti-inflammatory agents exhibit a synergistic whitening effect on the skin in combination with other active ingredients.

つぎに各種活性成分についてその色素沈着抑制作用を
評価した結果を示す。
Next, the results of evaluating the pigmentation inhibiting action of various active ingredients are shown.

試験方法: English系茶色モルモットの背部を剃毛して紫外線(U
VB強度:1J/cm2)を照射した。この操作を3日間繰り返
し、その間、リノール酸をはじめとする脂肪酸、あるい
は抗炎症剤を溶解した検体を紫外線照射部位に塗布し
た。10日間放置後、以下に示す判定基準に従い、色素沈
着度を肉眼判定した。
Test method: Shaving the back of English brown guinea pig,
VB intensity: 1 J / cm 2 ). This operation was repeated for 3 days, during which a sample in which a fatty acid such as linoleic acid or an anti-inflammatory agent was dissolved was applied to the ultraviolet irradiation site. After standing for 10 days, the degree of pigmentation was visually determined according to the following criteria.

判定基準: −:色素沈着は認められない ±:わずかな色素沈着が認められる +:中等度の色素沈着が認められる ++:強度の色素沈着を認められる 結果を次の第1表に示す。Criteria: −: No pigmentation is observed ±: Slight pigmentation is recognized +: Moderate pigmentation is recognized ++: Intense pigmentation is recognized The results are shown in Table 1 below.

第1表より明らかなごとく、炭素数18〜22かつ分子構
造中の不飽和結合数が2以上の遊離脂肪酸、その塩ある
いはアルキルエステルを単独で配合した場合、および抗
炎症剤を単独で配合した場合には、色素沈着の抑制作用
はわずかである。これに対して、抗炎症剤と前記脂肪酸
あるいはその誘導体を併用した場合は、顕著な色素沈着
の抑制作用が認められる。
As is evident from Table 1, when a free fatty acid having 18 to 22 carbon atoms and an unsaturated bond number in the molecular structure of 2 or more, a salt or an alkyl ester thereof was blended alone, and an anti-inflammatory agent was blended alone. In some cases, the effect of inhibiting pigmentation is slight. On the other hand, when the anti-inflammatory agent and the fatty acid or its derivative are used in combination, a remarkable inhibitory effect on pigmentation is observed.

本発明の美白化粧料は、公知の方法により、化粧水、
化粧用油、クリーム、乳液、パック、パウダーなどの形
態に製造される。
The whitening cosmetic of the present invention, by a known method, lotion,
It is manufactured in the form of cosmetic oils, creams, emulsions, packs, powders and the like.

さらに本発明の化粧料には、その種類に応じ性能を損
なわない範囲において、適宜公知の成分を配合すること
ができる。
Further, the cosmetic of the present invention may be appropriately blended with known components within a range that does not impair the performance according to the type.

なお、従来から使用されているメラミン産生抑制剤
(ビタミンC、胎盤抽出物)、紫外線吸収剤、紫外線散
乱剤、抗酸化剤などを配合しても良い。
A melamine production inhibitor (vitamin C, placenta extract), an ultraviolet absorber, an ultraviolet scattering agent, an antioxidant, and the like, which are conventionally used, may be added.

実施例 つぎに本発明を実施例によりさらに具体的に説明す
る。
EXAMPLES Next, the present invention will be described more specifically with reference to examples.

実施例1(化粧水) 精製水にグリセリン、クエン酸、クエン酸ナトリウ
ム、水溶性プラセンタエキスを溶解する。別個にエタノ
ールにアラントイン、ヨモギエキス、リノール酸、α−
リノレン酸、ポリオキシエチレン硬化ヒマシ油(60E.
O.)、メチルパラベン、香料を溶解し、前記の精製水溶
液に加えて可溶化し、ろ過して化粧水を得た。
Example 1 (Lotion) Dissolve glycerin, citric acid, sodium citrate, and water-soluble placenta extract in purified water. Separately, allantoin, mugwort extract, linoleic acid, α-
Linolenic acid, polyoxyethylene hydrogenated castor oil (60E.
O.), methylparaben and perfume were dissolved, added to the purified aqueous solution to solubilize, and filtered to obtain a lotion.

実施例2(化粧用油) スクワランに他の成分を均一に溶解して化粧用油を得
た。
Example 2 (cosmetic oil) Other ingredients were uniformly dissolved in squalane to obtain a cosmetic oil.

実施例3(クリーム) 成分(A)を加熱溶解し、80℃に保持する。別に香料
を除く成分(B)を加熱溶解して80℃に保ち、これに前
記成分(A)を撹拌しながら加え、充分混合する。さら
に撹拌しながら冷却を行い、香料を加え、さらに冷却し
てクリームを得た。
Example 3 (cream) The component (A) is dissolved by heating and kept at 80 ° C. Separately, the component (B) excluding the fragrance is dissolved by heating and kept at 80 ° C., and the component (A) is added thereto with stirring and mixed well. Cooling was further performed with stirring, a flavor was added, and further cooling was performed to obtain a cream.

実施例4(乳液) 成分(A)を80℃にて加熱溶解し、別に加温(80℃)
溶解した香料を除く成分(B)に撹拌しながら加え、充
分混合する。ついで、撹拌しながら冷却を行い、香料を
加え、さらに冷却して乳液を得た。
Example 4 (Emulsion) Ingredient (A) is heated and melted at 80 ° C and heated separately (80 ° C)
Add to the component (B) excluding the dissolved perfume with stirring and mix well. Then, the mixture was cooled with stirring, a fragrance was added, and the mixture was further cooled to obtain an emulsion.

実施例5(パック) 紫根エキス、アラントイン、α−リノレン酸、ドコサ
ヘキサエン酸、パラオキシ安息香酸エチル、香料および
エタノールを均一に溶解する。これを酢酸ビニル・スチ
レン共重合体、ポリビニルアルコール、ソルビット、感
光素301号およびカオリンを均一に混和したものに加え
る。これに、さらに水溶液プラセンタエキスを精製水に
均一に溶解した溶液を加え、均一に混和しパックを得
た。
Example 5 (pack) The purple root extract, allantoin, α-linolenic acid, docosahexaenoic acid, ethyl parahydroxybenzoate, flavor and ethanol are uniformly dissolved. This is added to a homogeneous mixture of vinyl acetate / styrene copolymer, polyvinyl alcohol, sorbit, photosensitizer No. 301 and kaolin. Further, a solution prepared by uniformly dissolving the aqueous placenta extract in purified water was added thereto, and the mixture was uniformly mixed to obtain a pack.

実施例6(パウダー) 塩酸ジフェンヒドラミン、ワレモコウエキス、リノエ
ライジン酸、リノール酸エチルおよびステアリン酸デカ
グリセリルを加熱溶解し、70℃に保持し、これをデキス
トリンおよびタルクの混合物に撹拌しながら徐々に加え
てパウダーを得た。
Example 6 (powder) Diphenhydramine hydrochloride, Waremoborg extract, linoleic acid, ethyl linoleate and decaglyceryl stearate were dissolved by heating and maintained at 70 ° C., and this was gradually added to a mixture of dextrin and talc with stirring to obtain a powder.

発明の効果 本発明化粧料は、皮膚に適用することにより、紫外線
による皮膚の黒化あるいは色素沈着を消失、もしくは予
防し優れた美白効果を発揮する。
Effect of the Invention The cosmetic of the present invention, when applied to the skin, eliminates or prevents blackening or pigmentation of the skin due to ultraviolet rays and exhibits an excellent whitening effect.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】(a)炭素数18〜22かつ分子構造中の不飽
和結合数が2以上の遊離脂肪酸、その塩、あるいは一価
または二価アルコールとのエステルからなる群より選ば
れた1種または2種以上の化合物および (b)イプシロンアミノカプロン酸、グリチルレチン
酸、グリチルリチン酸、その塩、およびその誘導体、感
光素301号、感光素401号、塩酸ジフェンヒドラミン、水
溶性アズレン、アデノシン一リン酸、カラミン、紫根エ
キス、当帰エキス、ヨモギエキス並びにワレモコウエキ
スから選ばれる1種または2種以上を配合したことを特
徴とする美白化粧料。
(1) a free fatty acid having 18 to 22 carbon atoms and having at least 2 unsaturated bonds in the molecular structure, a salt thereof, or an ester with a monohydric or dihydric alcohol; One or more compounds and (b) epsilon aminocaproic acid, glycyrrhetinic acid, glycyrrhizic acid, salts thereof, and derivatives thereof, photosensitizer 301, photosensitizer 401, diphenhydramine hydrochloride, water-soluble azulene, adenosine monophosphate, A whitening cosmetic comprising one or more selected from calamine, purple root extract, Toki extract, mugwort extract, and sagebrush extract.
JP63011583A 1988-01-20 1988-01-20 Whitening cosmetics Expired - Lifetime JP2608745B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63011583A JP2608745B2 (en) 1988-01-20 1988-01-20 Whitening cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63011583A JP2608745B2 (en) 1988-01-20 1988-01-20 Whitening cosmetics

Publications (2)

Publication Number Publication Date
JPH01186809A JPH01186809A (en) 1989-07-26
JP2608745B2 true JP2608745B2 (en) 1997-05-14

Family

ID=11781927

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63011583A Expired - Lifetime JP2608745B2 (en) 1988-01-20 1988-01-20 Whitening cosmetics

Country Status (1)

Country Link
JP (1) JP2608745B2 (en)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5686086A (en) * 1992-07-13 1997-11-11 Shiseido Co., Ltd. External skin treatment composition
DE69332818T3 (en) * 1992-07-13 2008-01-24 Shiseido Co. Ltd. COMPOSITION FOR DERMATOLOGICAL PREPARATION
US5962000A (en) * 1992-07-13 1999-10-05 Shiseido Company, Ltd. External skin treatment composition
JP3607062B2 (en) * 1997-10-24 2005-01-05 株式会社コーセー Fat accumulation inhibitor and skin external preparation containing the same
JP2000119156A (en) * 1998-10-14 2000-04-25 Kose Corp Skin lotion
KR20010060882A (en) * 1999-12-28 2001-07-07 서경배 A composition for external application for skin whitening
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