JP2644353B2 - Whitening cosmetics - Google Patents

Whitening cosmetics

Info

Publication number
JP2644353B2
JP2644353B2 JP313890A JP313890A JP2644353B2 JP 2644353 B2 JP2644353 B2 JP 2644353B2 JP 313890 A JP313890 A JP 313890A JP 313890 A JP313890 A JP 313890A JP 2644353 B2 JP2644353 B2 JP 2644353B2
Authority
JP
Japan
Prior art keywords
pigmentation
hydroxy
methoxybenzophenone
acid
whitening
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 - Fee Related
Application number
JP313890A
Other languages
Japanese (ja)
Other versions
JPH03209305A (en
Inventor
義之 石倉
真理奈 永田
秀典 兼久
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.)
SANSUTAA KK
Original Assignee
SANSUTAA KK
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 SANSUTAA KK filed Critical SANSUTAA KK
Priority to JP313890A priority Critical patent/JP2644353B2/en
Publication of JPH03209305A publication Critical patent/JPH03209305A/en
Application granted granted Critical
Publication of JP2644353B2 publication Critical patent/JP2644353B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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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
バカスなどの皮膚の色素沈着を消失、淡色化または予防
する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 that eliminates, darkens, or prevents skin blackening due to ultraviolet rays or skin pigmentation such as spots and freckles.

従来の技術および課題 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シナ
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、充分な色素沈着の消失
もしくは淡色化などの効果は得られず、また、刺激等の
副作用の問題があった。
2. Description of the Related Art Conventionally, as a whitening cosmetic composition, a composition containing a tyrosinase activity inhibitor such as vitamin C and a derivative thereof, a reducing agent, and a 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 it is actually applied to the skin, sufficient effects such as disappearance of pigmentation or lightening are not obtained, and there are problems of side effects such as irritation.

課題を解決するための手段 本発明者らは、美白化粧料について鋭意研究を重ねた
結果、以外にも、特定の脂肪酸またはその誘導体と、さ
らに2−ヒドロキシ−4−メトキシベンゾフェノンを組
み合わせることにより皮膚の色素沈着の消失、もしくは
淡色化に優れた相乗的な効果が現れ、さらに、刺激等の
抑制された美白化粧料が得ら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 on whitening cosmetics, and have also obtained a combination of a specific fatty acid or a derivative thereof and 2-hydroxy-4-methoxybenzophenone, The present inventors have found that a synergistic effect excellent in the disappearance of pigmentation or lightening is obtained, and that a whitening cosmetic product with suppressed irritation and the like can be obtained, thereby completing the present invention.

すなわち、本発明は、 (a)2−ヒドロキシ−4−メトキシベンゾフェノン、
および (b)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) 2-hydroxy-4-methoxybenzophenone,
And (b) having 18 to 22 carbon atoms and 2 unsaturated bonds in the molecular structure.
A whitening cosmetic comprising the above free fatty acid, a salt thereof, or an ester with a monohydric or dihydric alcohol is provided.

本発明の美白化粧料に配合される2−ヒドロキシ−4
−メトキシベンゾフェノンは、従来、紫外線吸収剤とし
て公知の化粧品原料であるが、他の活性成分と組み合わ
せて皮膚に対し相乗的な美白効果を示すことについては
未だ知られていない。
2-hydroxy-4 compounded in the whitening cosmetic composition of the present invention
-Methoxybenzophenone is a cosmetic raw material conventionally known as an ultraviolet absorber, but it is not yet known to exhibit a synergistic whitening effect on the skin in combination with other active ingredients.

本発明においては、美白効果の点から、この2−ヒド
ロキシ−4−メトキシベンゾフェノンを化粧料全量に対
して0.001〜10重量%の割合で配合するが好ましい。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。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以上の代表的なものとしては、遊離脂肪酸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。
In the present invention, from the viewpoint of a whitening effect, it is preferable to add the 2-hydroxy-4-methoxybenzophenone at a ratio of 0.001 to 10% by weight based on the total amount of the cosmetic. In blending linoleic acid and the like in the cosmetic of the present invention, it is preferable to use a purified product. Typical examples of the whitening cosmetic of the present invention having 18 to 22 carbon atoms and having 2 or more unsaturated bonds in the molecular structure include the free fatty acid γ.
-Linolenic acid, arachidonic acid, eicosapentaenoic acid and the like, and one or more of these are used.

これらの脂肪酸は、通常、動植物油脂中のトリグリセ
リドから遊離されるものであるが、トリグリセリド自体
は遊離脂肪酸やそのアルキルエステルのように動物試験
等において優れた色素沈着淡色化作用を示さない。ま
た、動植物油脂中にはパルチメン酸やステアリン酸など
の飽和脂肪酸を含むものもあるが、これら飽和脂肪酸も
色素沈着抑制効果を示さず、場合により、逆にメラニン
産生を亢進することもある。したがって、これらの脂肪
酸は充分に精製したものを用いることが好ましい。
These fatty acids are usually released from triglycerides in animal and vegetable oils and fats, but triglycerides themselves do not show an excellent pigmentation and lightening effect in animal tests and the like like free fatty acids and alkyl esters thereof. In addition, some animal and vegetable fats and oils contain saturated fatty acids such as partimic acid and stearic acid. However, these saturated fatty acids do not show a pigmentation-suppressing effect, and may increase melanin production in some cases. Therefore, it is preferable to use a sufficiently purified fatty acid.

また、これら脂肪酸の塩としては、ナトリウム塩、カ
リウム塩等のアルカリ金属塩、アルギニン塩、リジン塩
等のアミノ酸塩、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が挙げられる。
Examples of the salts of these fatty acids include alkali 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、該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等の一価
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等の二価ア
ルコールとのエステル等が挙げられる。
Further, examples of the alkyl ester of the 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.

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、色素沈着の淡
色化効果がなく、一方、10重量%を越えると、刺激性が
強い。
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, there is no lightening effect of pigmentation, and when the amount exceeds 10% by weight, irritation is strong.

つぎに各種成分についてその色素沈着の消失もしくは
淡色化の作用と脂肪酸による皮膚刺激の抑制作用を評価
した結果を示す。
Next, the results of evaluating the effects of various components on the disappearance or lightening of pigmentation and on the effect of suppressing fatty acid irritation by skin are shown.

試験方法: 実験1 JY−3系茶色モルモットの背部を剃毛して紫外線(UV
B強度:1J/cm2)を照射し、1週間後に色素沈着を得た。
つぎに、この部位に、2−ヒドロキシ−4−メトキシベ
ンゾフェノン、リノール酸をはじめとする種々の成分を
エタノールに溶解した検体を4週間累積塗布した。色素
沈着の淡色化の評価は、検体を塗布していない部位(無
塗布)の色素沈着度を0とし、その淡色化の度合によ
り、以下に示す判定基準に従って色素沈着度を肉眼判定
することにより行った。
Test method: Experiment 1 Shaving the back of JY-3 brown guinea pig,
B intensity: 1 J / cm 2 ), and one week later, pigmentation was obtained.
Next, samples obtained by dissolving various components such as 2-hydroxy-4-methoxybenzophenone and linoleic acid in ethanol were cumulatively applied to this site for 4 weeks. The pigmentation lightening was evaluated by setting the degree of pigmentation of a part to which the sample was not applied (uncoated) to 0, and visually determining the degree of pigmentation according to the following criteria based on the degree of the lightening. went.

判定基準: 0:色素沈着の淡色化が認められない。Judgment criteria: 0: No lightening of pigmentation was observed.

−1:わずかに色素沈着の淡色化が認められる。-1: slight fading of pigmentation is observed.

−2:中等度の色素沈着の淡色化が認められる。-2: Lightening of moderate pigmentation is observed.

−3:顕著な色素沈着の淡色化が認められる。−3: Remarkable lightening of pigmentation is observed.

結果を以下の第1表および第2表に示す。 The results are shown in Tables 1 and 2 below.

第1表および第2表より明らかなごとく、2−ヒドロ
キシ−4−メトキシベンゾフェノン単独では色素沈着の
淡色化は認められず、また炭素数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は、色素沈着の
淡色化はわずかである。これらに対して、2−ヒドロキ
シ−4−メトキシ−ベンゾフェノンと前記脂肪酸あるい
はその誘導体を併用した場合は、顕著な色素沈着が認め
られる。
As is clear from Tables 1 and 2, 2-hydroxy-4-methoxybenzophenone alone did not show any fading of pigmentation, and had 18 to 22 carbon atoms and 2 or more unsaturated bonds in the molecular structure. When only the free fatty acid, its salt or alkyl ester is blended alone, the coloration of pigmentation is slightly reduced. On the other hand, when 2-hydroxy-4-methoxy-benzophenone is used in combination with the above fatty acid or its derivative, remarkable pigmentation is observed.

実験2 健常人10名の上腕内側部にはパッチ・テスト用判創膏
を用い、2−ヒドロキシ−4−メトキシベンゾフェノン
およびリノール酸をエッセンスベースに配合した検体を
24時間閉塞貼布した。皮膚刺激の程度を評価する方法と
して、紅斑および浮腫を以下に示す判定基準に従って肉
眼判定した。
Experiment 2 A patch test patch containing 2-hydroxy-4-methoxybenzophenone and linoleic acid was used as an essence base on the inner side of the upper arm of 10 healthy subjects.
Closure was applied for 24 hours. As a method for evaluating the degree of skin irritation, erythema and edema were visually determined according to the following criteria.

判定基準 0:変化なし 0.5:不明瞭な紅斑 1:明瞭な紅斑 2:紅斑および浮腫 10名の判定測定値の平均を100倍した値を皮膚障害指
数とし、その結果を第3表に示す。
Criteria 0: No change 0.5: Indistinct erythema 1: Clear erythema 2: Erythema and edema A value obtained by multiplying the average of the measured values of 10 subjects by 100 is defined as a skin damage index, and the results are shown in Table 3.

第3表より明らかなごとく、2−ヒドロキシ−4−メ
トキシベンゾフェノンには、脂肪酸による皮膚刺激の抑
制作用が認められる。
As is clear from Table 3, 2-hydroxy-4-methoxybenzophenone has an inhibitory effect of fatty acids on skin irritation.

かくして、本発明の美白化粧料は、2−ヒドロキシ−
4−メトキシベンゾフェノンおよび該脂肪酸またはその
誘導体を公知の方法により所望の他の成分と合し、化粧
水、化粧用油、クリーム、乳液、パック、パウダー等の
形態に製造される。
Thus, the whitening cosmetic composition of the present invention comprises 2-hydroxy-
4-Methoxybenzophenone and the fatty acid or a derivative thereof are combined with other desired components by a known method to produce a lotion, a cosmetic oil, a cream, a milky lotion, a pack, a powder and the like.

他の配合成分は特に限定するものではなく、化粧料の
種類に応じて性能を損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。
The other components are not particularly limited, and known components can be appropriately compounded within a range that does not impair the performance according to the type of the cosmetic.

なお、従来から使用されているメラニン産生抑制剤
(ビタミンC、胎盤抽出物)、紫外線吸収剤、紫外線散
乱剤、抗炎症剤、抗酸化剤等をさらに配合してもよい。
A conventionally used melanin production inhibitor (vitamin C, placenta extract), an ultraviolet absorber, an ultraviolet scattering agent, an anti-inflammatory agent, an antioxidant, and the like may be further 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.

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2−ヒドロキシ−4−メトキシベンゾフェノン、
リノール酸、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、濾過して化粧水を得た。
Dissolve glycerin, citric acid, sodium citrate, and water-soluble placenta extract in purified water. 2-hydroxy-4-methoxybenzophenone separately in ethanol,
Linoleic 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.

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。
Other ingredients were uniformly dissolved in squalane to obtain a cosmetic oil.

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。
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.

成分(A)を80℃にて加熱し、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。
The component (A) is heated at 80 ° C., and is separately heated (80 ° C.) and added to the component (B) excluding the dissolved fragrance while stirring, and mixed well. Then, the mixture was cooled with stirring, a fragrance was added, and the mixture was further cooled to obtain an emulsion.

2−ヒドロキシ−4−メトキシベンゾフェノン、リノ
ール酸、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、酸化チタンおよびカオリンを均一に混
和したものに加える。これに、さらに水溶性プラセンタ
エキス、パラオキシ安息香酸エチル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。
Dissolve 2-hydroxy-4-methoxybenzophenone, linoleic acid, flavor and ethanol uniformly. This is added to a homogeneous mixture of vinyl acetate / styrene copolymer, polyvinyl alcohol, sorbite, titanium oxide and kaolin. To this, a solution in which a water-soluble placenta extract and ethyl parahydroxybenzoate were uniformly dissolved in purified water was added, and the mixture was uniformly mixed to obtain a pack.

2−ヒドロキシ−4−メトキシベンゾフェノン、リノ
ール酸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。
2-Hydroxy-4-methoxybenzophenone, linoleic acid 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、淡色化もし
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, darkens 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)2−ヒドロキシ−4−メトキシベン
ゾフェノン、および (b)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を配合したことを特徴とする美白化
粧料。
(1) 2-hydroxy-4-methoxybenzophenone (a), and (b) a compound having 18 to 22 carbon atoms and an unsaturated bond number of 2 in a molecular structure.
A whitening cosmetic comprising the above free fatty acid, a salt thereof or an ester with a monohydric or dihydric alcohol.
JP313890A 1990-01-10 1990-01-10 Whitening cosmetics Expired - Fee Related JP2644353B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP313890A JP2644353B2 (en) 1990-01-10 1990-01-10 Whitening cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP313890A JP2644353B2 (en) 1990-01-10 1990-01-10 Whitening cosmetics

Publications (2)

Publication Number Publication Date
JPH03209305A JPH03209305A (en) 1991-09-12
JP2644353B2 true JP2644353B2 (en) 1997-08-25

Family

ID=11548992

Family Applications (1)

Application Number Title Priority Date Filing Date
JP313890A Expired - Fee Related JP2644353B2 (en) 1990-01-10 1990-01-10 Whitening cosmetics

Country Status (1)

Country Link
JP (1) JP2644353B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07291850A (en) * 1994-04-26 1995-11-07 Kanebo Ltd Skin cosmetic
WO2008047633A1 (en) * 2006-10-10 2008-04-24 Maruha Corporation Aliphatic compound-containing skin whitening agent

Also Published As

Publication number Publication date
JPH03209305A (en) 1991-09-12

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