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JP2764510B2 - Whitening cosmetics - Google Patents

Whitening cosmetics

Info

Publication number
JP2764510B2
JP2764510B2 JP4348612A JP34861292A JP2764510B2 JP 2764510 B2 JP2764510 B2 JP 2764510B2 JP 4348612 A JP4348612 A JP 4348612A JP 34861292 A JP34861292 A JP 34861292A JP 2764510 B2 JP2764510 B2 JP 2764510B2
Authority
JP
Japan
Prior art keywords
extract
urea
whitening
added
skin
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
JP4348612A
Other languages
Japanese (ja)
Other versions
JPH06199646A (en
Inventor
直樹 加藤
恒雄 進邦
光晴 増田
裕二 鈴木
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP4348612A priority Critical patent/JP2764510B2/en
Publication of JPH06199646A publication Critical patent/JPH06199646A/en
Application granted granted Critical
Publication of JP2764510B2 publication Critical patent/JP2764510B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Cosmetics (AREA)
  • Medicines Containing Plant Substances (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は美白化粧料、更に詳しく
は安全性が高く、皮膚美白効果に優れ、日焼け等による
シミ及びソバカスを予防及び治療することのできる美白
化粧料に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a whitening cosmetic, and more particularly to a whitening cosmetic which is highly safe, has an excellent skin whitening effect, and can prevent and treat spots and freckles caused by sunburn.

【0002】[0002]

【従来の技術】皮膚のシミ及びソバカスは一般に日光か
らの紫外線暴露による刺激やホルモンの異常、あるいは
遺伝的要素などが原因となってメラノサイトが活性化さ
れ、そこで合成されたメラニン色素が皮膚内に異常沈着
して発生するものと考えられている。
2. Description of the Related Art In general, skin spots and freckles are activated by melanocytes due to irritation caused by exposure to ultraviolet rays from sunlight, hormonal abnormalities, or genetic factors. Melanin pigments synthesized there are deposited in the skin. It is thought to be caused by abnormal deposition.

【0003】従来、このようなシミやソバカスを防ぐた
めに様々な美白化粧料が提供されてきたが、その中でも
植物抽出物(エキス)を化粧料に応用した例は多く、シ
ミ、ソバカスを予防及び治療する美白効果を有するもの
についてが報告されている。
Conventionally, various whitening cosmetics have been provided in order to prevent such stains and freckles. Among them, there are many examples of applying a plant extract (extract) to cosmetics. Those that have a whitening effect to treat are reported.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、一般に
植物抽出物は皮膚への浸透性は低く、そのためにこれを
配合した化粧料は美白効果が充分に発揮されないという
問題がある。そこで、このような有効成分の皮膚浸透性
を向上させる浸透促進剤の研究もなされているが、これ
までのところ浸透促進効果を有するものは安全性の面で
劣り、化粧料への応用には依然問題がある。
However, plant extracts generally have low permeability to the skin, and therefore, there is a problem that cosmetics containing the same do not exhibit a sufficient whitening effect. Therefore, studies have been made on penetration enhancers that improve the skin permeability of such active ingredients.However, those having a penetration promotion effect are so far inferior in safety and are not suitable for application to cosmetics. There are still problems.

【0005】従って、植物抽出物を含有し、安全性に優
れると共に、皮膚への浸透性が高く、シミ及びソバカス
を予防及び治療することができる美白化粧料の開発が望
まれていた。
[0005] Therefore, there has been a demand for the development of a whitening cosmetic which contains a plant extract, is excellent in safety, has high permeability to the skin, and can prevent and treat spots and freckles.

【0006】[0006]

【課題を解決するための手段】かかる実情において、本
発明者らは鋭意検討を行った結果、特定の植物抽出物に
尿素及び尿素安定化剤を併用することにより、皮膚浸透
性に優れ、美白効果が良好で、かつ安全性の高い美白化
粧料の得られることを見出し、本発明を完成するに至っ
た。
Under such circumstances, the present inventors have conducted intensive studies. As a result, the combined use of a specific plant extract with urea and a urea stabilizer has excellent skin penetration and whitening. The present inventors have found that a whitening cosmetic having good effects and high safety can be obtained, and the present invention has been completed.

【0007】すなわち、本発明は次の成分(A)、
(B)及び(C) (A)チョウジ抽出物、緑茶抽出物、葛根抽出物、桑白
皮抽出物、甘草抽出物、オウゴン抽出物、アロエ抽出物
及び橙皮抽出物から選ばれる植物抽出物の一種又は二種
以上 (B)尿素 (C)尿素安定化剤を含有する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 the following component (A):
(B) and (C) (A) A plant extract selected from a clove extract, a green tea extract, a radish extract, a mulberry bark extract, a licorice extract, a gougon extract, an aloe extract and an orange peel extract (B) urea (C) A whitening cosmetic characterized by containing a urea stabilizer.

【0008】本発明で用いられる成分(A)の植物抽出
物としては、チョウジ、緑茶、葛根、桑白皮、甘草、オ
ウゴン、アロエ若しくは橙皮を水やエタノール、メタノ
ール、1,3−ブチレングリコール、プロピレングリコ
ール等の親水性有機溶媒又はこれらの混合溶媒で抽出し
て得られる抽出液又は当該抽出液を乾燥して得られる乾
燥粉末などを用いることができる。
[0008] The plant extract of the component (A) used in the present invention includes butterflies, green tea, kakkon, mulberry bark, licorice, Japanese gourd, aloe or orange peel with water, ethanol, methanol, 1,3-butylene glycol. And an extract obtained by extraction with a hydrophilic organic solvent such as propylene glycol or a mixed solvent thereof, or a dry powder obtained by drying the extract.

【0009】例えばチョウジの抽出物を得るには、チョ
ウジのつぼみを乾燥して細切りし、これに水/エタノー
ル混合液を加え、時々攪拌した後室温で浸漬し、圧搾分
離して抽出液を得た後、ろ過すればよい。
For example, in order to obtain an extract of a clove, a bud of a clove is dried and cut into small pieces, a water / ethanol mixture is added thereto, and the mixture is occasionally stirred, immersed at room temperature, and pressed and separated to obtain an extract. After that, it may be filtered.

【0010】また、成分(A)の植物抽出物としては市
販のものを用いることができ、かかる市販品としては、
例えばファルコレックス チョウジ、緑茶リキッド、カ
ッコンエキスパウダー、ファルコレックス ソウハク
ヒ、オウゴンエキスパウダー、オウゴンリキッド、アロ
エMS、トウヒエキスパウダー(以上、一丸ファルコス
(株)製)、油溶性甘草エキス(丸善製薬(株)製)等
が挙げられる。
[0010] As the plant extract of the component (A), commercially available ones can be used.
For example, Falco Rex Clove, Green Tea Liquid, Cuckoo Extract Powder, Falco Rex Sohakuhi, Ougon Extract Powder, Ougon Liquid, Aloe MS, Spruce Extract Powder (all manufactured by Ichimaru Falcos Co., Ltd.), Oil-soluble Licorice Extract (Maruzen Pharmaceutical Co., Ltd.) Manufactured).

【0011】成分(A)の植物抽出物は、一種を単独で
も、又は二種以上を組合わせて用いることができ、全組
成中に固形分として0.001〜20重量%(以下、単
に%で示す)、特に0.005〜10%配合するのが好
ましい。
The plant extract of the component (A) may be used alone or in combination of two or more, and 0.001 to 20% by weight (hereinafter simply referred to as “% It is particularly preferable to add 0.005 to 10%.

【0012】本発明に用いられる成分(B)の尿素は、
全組成中に0.05〜10%、特に0.2〜5%配合さ
れるのが好ましい。配合量が0.05%未満では充分な
効果が得られず、10%を超えて配合してもそれに見合
った効果は得られない。
The urea of component (B) used in the present invention is
It is preferable that 0.05 to 10%, particularly 0.2 to 5% is blended in the whole composition. If the amount is less than 0.05%, a sufficient effect cannot be obtained, and if the amount exceeds 10%, a corresponding effect cannot be obtained.

【0013】また、本発明に用いられる成分(C)の尿
素安定化剤は、水溶液中での尿素の分解を抑制し、安定
化する化合物であれば特に限定されないが、具体例とし
ては、乳酸、脂肪族ジカルボン酸、アラントイン、アン
モニウム化合物、6−アミノ−n−カプロン酸に代表さ
れるアミノカルボン酸、グリシンに代表されるアミノ酸
及びその塩、ニコチン酸及びその誘導体等が挙げられ
る。
The urea stabilizer of component (C) used in the present invention is not particularly limited as long as it suppresses and stabilizes urea in an aqueous solution. And aliphatic dicarboxylic acids, allantoin, ammonium compounds, aminocarboxylic acids represented by 6-amino-n-caproic acid, amino acids represented by glycine and salts thereof, nicotinic acid and derivatives thereof.

【0014】成分(C)の尿素安定化剤は、一種を単独
でも、又は二種以上を組合わせて用いることができ、有
効な配合量は尿素安定化剤の種類によって異なるが、一
般に成分(B)の尿素に対して、5〜200%、特に1
0〜100%配合するのが好ましい。
The urea stabilizer of the component (C) can be used alone or in combination of two or more. The effective amount of the urea stabilizer depends on the type of the urea stabilizer. 5 to 200%, especially 1%, based on urea of B)
It is preferable to mix 0 to 100%.

【0015】更に、本発明の美白化粧料には、前記必須
成分の他、通常の化粧料、医薬部外品、医薬品等に用い
られる各種任意成分、例えば油剤、保湿剤、増粘剤、防
腐剤、乳化剤、顔料、粉体、pH調整剤、薬効成分、紫外
線吸収剤、抗酸化剤、香料等を適宜配合することができ
る。
Furthermore, in addition to the above essential components, various optional components used in ordinary cosmetics, quasi-drugs, pharmaceuticals, etc., such as oils, humectants, thickeners, preservatives, etc. Agents, emulsifiers, pigments, powders, pH adjusters, medicinal ingredients, ultraviolet absorbers, antioxidants, fragrances, and the like can be appropriately compounded.

【0016】具体的には、油剤としては流動パラフィ
ン、ワセリン、パラフィンワックス、スクワラン、ミツ
ロウ、カルナウバロウ、オリーブ油、ラノリン、高級ア
ルコール、脂肪酸、高級アルコールと脂肪酸の合成エス
テル油、シリコーン油等が挙げられ、保湿剤としてはソ
ルビトール、キシリトール、グリセリン、マルチトー
ル、プロピレングリコール、ピロリドンカルボン酸ナト
リウム、ポリオキシプロピレン脂肪酸エステル、ポリエ
チレングリコール等が挙げられ、増粘剤としてはカルボ
キシビニルポリマー、カルボキシメチルセルロース、ポ
リビニルアルコール、カラギーナン、ゼラチン等の水溶
性高分子、塩化ナトリウム、塩化カリウム等の電解質な
どが挙げられ、防腐剤としてはメチルパラベン、エチル
パラベン、プロピルパラベン、ブチルパラベン、安息香
酸ナトリウム等が挙げられ、乳化剤としてはポリオキシ
エチレンアルキルエーテル、ポリオキシエチレン脂肪酸
エステル、ポリオキシエチレンソルビタン脂肪酸エステ
ル、グリセリン脂肪酸エステル、ポリグリセリン脂肪酸
エステル、ポリオキシエチレングリセリン脂肪酸エステ
ル、ポリオキシエチレン硬化ヒマシ油、ポリオキシエチ
レンソルビトール脂肪酸エステル等の非イオン界面活性
剤が挙げられ、粉体としてはタルク、セリサイト、マイ
カ、カオリン、シリカ、ベントナイト、バーミキュライ
ト、亜鉛華、雲母、雲母チタン、酸化チタン、酸化マグ
ネシウム、酸化ジルコニウム、硫酸バリウム、ベンガ
ラ、酸化鉄、群青等が挙げられ、pH調整剤としてはクエ
ン酸−クエン酸ナトリウム等の緩衝剤が挙げられ、薬効
成分としては、アルブチン、コウジ酸、ビタミンC及び
その誘導体、プラセンタエキス、グリチルリチン酸ジカ
リウム等が挙げられる。
Specifically, examples of oils include liquid paraffin, vaseline, paraffin wax, squalane, beeswax, carnauba wax, olive oil, lanolin, higher alcohols, fatty acids, synthetic ester oils of higher alcohols and fatty acids, silicone oils, and the like. Examples of the humectant include sorbitol, xylitol, glycerin, maltitol, propylene glycol, sodium pyrrolidonecarboxylate, polyoxypropylene fatty acid ester, and polyethylene glycol. And water-soluble polymers such as gelatin, and electrolytes such as sodium chloride and potassium chloride. Examples of preservatives include methyl paraben, ethyl paraben, and propyl paraben. Ben, butylparaben, sodium benzoate, etc., and as the emulsifier, polyoxyethylene alkyl ether, polyoxyethylene fatty acid ester, polyoxyethylene sorbitan fatty acid ester, glycerin fatty acid ester, polyglycerin fatty acid ester, polyoxyethylene glycerin fatty acid ester And non-ionic surfactants such as polyoxyethylene hydrogenated castor oil and polyoxyethylene sorbitol fatty acid ester. Examples of powders include talc, sericite, mica, kaolin, silica, bentonite, vermiculite, zinc white, mica, and mica Titanium, titanium oxide, magnesium oxide, zirconium oxide, barium sulfate, red iron oxide, iron oxide, ultramarine and the like, and as the pH adjuster, citric acid-sodium citrate and other buffering agents The pharmaceutically active ingredients include arbutin, kojic acid, vitamin C and its derivatives, placenta extract, dipotassium glycyrrhizinate and the like.

【0017】本発明の美白化粧料は常法に従って製造す
ることができる。また、本発明の対象となる美白化粧料
は、一般皮膚化粧料に限定されるものではなく、医薬部
外品、外用医薬品等を包含するものであり、その剤型も
クリーム、乳液、化粧水、ファンデーション、パック、
ローション状、ゲル状、溶液状、スティック状等、その
目的に応じて任意に選択することができる。
The whitening cosmetic of the present invention can be produced according to a conventional method. Further, the whitening cosmetics that are the subject of the present invention are not limited to general skin cosmetics, but include quasi-drugs, external medicines, and the like, and their dosage forms are creams, emulsions, and lotions. , Foundation, pack,
Lotions, gels, solutions, sticks, etc. can be arbitrarily selected according to the purpose.

【0018】[0018]

【発明の効果】本発明の美白化粧料は、特定の植物抽出
物と尿素と尿素安定化剤を併用することにより、植物抽
出物の皮膚浸透性が高められ、優れた美白効果と、日焼
け等によるシミ及びソバカスの予防及び治療効果を有
し、かつ安全性も高いものである。
EFFECT OF THE INVENTION The skin-whitening cosmetic composition of the present invention has enhanced skin permeability of the plant extract by using urea and a urea stabilizer in combination with a specific plant extract, and has an excellent whitening effect and sunburn. Has a preventive and therapeutic effect on spots and freckles, and is also highly safe.

【0019】[0019]

【実施例】以下に本発明を実施例により具体的に説明す
るが、本発明はこれらによって限定されるものではな
い。なお、以下の実施例において、皮膚浸透性の評価、
及び美白効果の評価は下記の方法により行った。
EXAMPLES The present invention will be described below in more detail with reference to examples, but the present invention is not limited by these examples. In the following examples, evaluation of skin permeability,
The evaluation of the whitening effect was performed by the following method.

【0020】皮膚浸透性の評価 豚皮背部を除毛し、表面を洗浄した後、4cm四方の小片
に裁断する。以下に示す実施例及び比較例の試料40μ
lを、調製した豚皮に塗布し、室温に放置する。表面に
残存する未浸透成分を除去した後、浸透成分を抽出回収
し、HPLCにて植物抽出物の浸透量を測定した。浸透
量は塗布面積当たりの値(μg/cm2)で表した。
Evaluation of skin permeability The back of pig skin is depilated, the surface is washed, and cut into small pieces of 4 cm square. Samples of Examples and Comparative Examples 40 μm shown below
1 is applied to the prepared pigskin and left at room temperature. After removing the unpermeated components remaining on the surface, the permeated components were extracted and collected, and the permeation amount of the plant extract was measured by HPLC. The amount of permeation was expressed as a value per coated area (μg / cm 2 ).

【0021】UV−B誘導色素斑に対する美白効果試験 健常男子被験者20名の上腕内側部に、UV−B領域の
紫外線を最小紅斑量の2倍量、1日1回2日間にわたり
照射し、誘導した色素斑に1日2回、1カ月間被験部位
に試料を連続塗布することによる美白効果を調べた。評
価は、色差計(村上色彩製、CMS−1200)を用い
て測定を行い、得られたマンセル値よりL*値を算出
し、その回復を表すΔΔL*値を用いた。なお、ΔΔL*
値は以下のように定義した。試料塗布開始直前の試料塗
布被験部位及び試料未塗布被験部位のL*値をそれぞれ
0、L0′、連続塗布1カ月後の各々の部位のL*値を
それぞれL1、L1′としてΔΔL*は以下の式で表し
た。 ΔΔL*=(L1−L0)−(L1′−L0′) また、評価は被験者20名の平均値で示した。評価点と
判定基準との関係を表1に示す。
Test of Whitening Effect on UV-B-Induced Pigment Spots The inner arm of 20 healthy male subjects was irradiated with ultraviolet rays in the UV-B region twice the minimum erythema dose once a day for 2 days. The whitening effect by continuously applying the sample to the test site twice a day on the pigmented spot thus obtained for one month was examined. The evaluation was performed using a color difference meter (CMS-1200, manufactured by Murakami Color Co., Ltd.), the L * value was calculated from the obtained Munsell value, and the ΔΔL * value representing the recovery was used. Note that ΔΔL *
The values were defined as follows: The sample application test site and the sample uncoated test site of the sample application immediately before the L * value, respectively L 0, L 0 ', the site of the L * value of each of the post-continuous coating 1 month L 1, L 1', respectively as ΔΔL * was represented by the following equation. ΔΔL * = (L 1 −L 0 ) − (L 1 ′ −L 0 ′) Further, the evaluation was shown by the average value of 20 subjects. Table 1 shows the relationship between the evaluation points and the criteria.

【0022】[0022]

【表1】 [Table 1]

【0023】なお、以下の実施例において、液状の植物
抽出物を使用した場合の配合量は、液体としての重量%
で示した。
In the following examples, when a liquid plant extract is used, the compounding amount is as follows:
Indicated by

【0024】実施例1 表2に示す組成のクリームを下記の方法により調製し、
皮膚浸透性の評価及び連続塗布による美白効果について
の評価を行った。皮膚浸透量は葛根抽出物の主成分であ
るプエラリンの浸透量を示した。以上の結果を表2に併
せて示す。 (調製方法)油相成分(1)〜(6)を80℃で加熱溶
解したものに、攪拌しながら80℃に加熱した水相成分
(7)〜(14)を加えて乳化した後(15)を加え、
攪拌しながら室温まで冷却した。
Example 1 A cream having the composition shown in Table 2 was prepared by the following method.
Evaluation of skin permeability and evaluation of whitening effect by continuous application were performed. The amount of skin permeation was the amount of puerarin, the main component of Kakkon extract. The results are shown in Table 2. (Preparation method) After the oil phase components (1) to (6) were dissolved by heating at 80 ° C., the aqueous phase components (7) to (14) heated to 80 ° C. were added with stirring and emulsified (15). )
It was cooled to room temperature with stirring.

【0025】[0025]

【表2】 [Table 2]

【0026】表2より明らかなように、本発明品は植物
抽出物の皮膚浸透性が有意に高く、美白効果も優れたも
のであった。
As is clear from Table 2, the product of the present invention had significantly higher skin permeability of the plant extract and an excellent whitening effect.

【0027】実施例2 表3に示す組成のエッセンス(美容液)を下記の方法に
より調製し、連続塗布による美白効果についての評価を
行った。その結果を併せて表4に示す。 (調製方法)(1)〜(5)の成分を攪拌分散した後、
これに精製水(11)65部を加えAとした。一方、
(6)、(7)、(12)、(13)の成分を攪拌溶解
した後、これに残量の精製水(11)を加えBとした。
Aを攪拌しながらBを加え均一にした後、(8)〜(1
0)の成分を加え、攪拌溶解した。
Example 2 Essences (cosmetics) having the compositions shown in Table 3 were prepared by the following method, and the whitening effect by continuous application was evaluated. Table 4 also shows the results. (Preparation method) After stirring and dispersing the components (1) to (5),
To this, 65 parts of purified water (11) was added to give A. on the other hand,
After the components (6), (7), (12) and (13) were stirred and dissolved, the remaining amount of purified water (11) was added to the mixture to give B.
After B was added to A while stirring to make it uniform, (8) to (1)
The component (0) was added and dissolved by stirring.

【0028】[0028]

【表3】 [Table 3]

【0029】[0029]

【表4】 [Table 4]

【0030】表4より明らかなように、本発明品は美白
効果に優れていることがわかる。
As is clear from Table 4, the product of the present invention has an excellent whitening effect.

【0031】[0031]

【表5】 実施例3 乳液:以下にその組成を示す乳液を下記方
法により調製した。 (組成) (重量%) (1)トリステアリン酸ポリオキシエチレンソルビタン 1.0 (2)オレイン酸グリセリル 1.0 (3)モノステアリン酸グリセリル 0.5 (4)スクワラン 6.0 (5)トリオクタン酸グリセリル 2.0 (6)オクタン酸セチル 2.0 (7)ステアリルアルコール 2.0 (8)メトキシケイ皮酸オクチル 2.0 (9)1,3−ブチレングリコール 5.0 (10)グリセリン 3.0 (11)緑茶抽出物*10 5.0 (12)尿素 2.0 (13)ニコチン酸アミド 1.0 (14)精製水 残量 (15)防腐剤 適量 (16)香料 適量 *10 :一丸ファルコス(株)製,緑茶リキッド(固形
分:1.0〜2.5重量%)
Example 3 Emulsion: An emulsion having the following composition was prepared by the following method. (Composition) (% by weight) (1) Polyoxyethylene sorbitan tristearate 1.0 (2) Glyceryl oleate 1.0 (3) Glyceryl monostearate 0.5 (4) Squalane 6.0 (5) Trioctane Glyceryl acid 2.0 (6) Cetyl octoate 2.0 (7) Stearyl alcohol 2.0 (8) Octyl methoxycinnamate 2.0 (9) 1,3-butylene glycol 5.0 (10) Glycerin 3 0.0 (11) Green tea extract * 10 5.0 (12) Urea 2.0 (13) Nicotinamide 1.0 (14) Remaining purified water (15) Preservatives appropriate amount (16) Flavors appropriate amount * 10: Green tea liquid (solid content: 1.0-2.5% by weight) manufactured by Ichimaru Falcos Co., Ltd.

【0032】(調製方法)油相成分(1)〜(8)を8
0℃で加熱溶解したものに、攪拌しながら80℃に加熱
した水相成分(9)〜(15)を加えて乳化した後、
(16)を加え攪拌しながら室温まで冷却した。
(Preparation method) The oil phase components (1) to (8)
After the aqueous phase components (9) to (15) heated to 80 ° C. while being stirred and added to the solution heated and dissolved at 0 ° C. and emulsified,
(16) was added and the mixture was cooled to room temperature with stirring.

【0033】[0033]

【表6】 実施例4 化粧水:以下にその組成を示す化粧水を下
記方法により調製した。 (組成) (重量%) (1)1,3−ブチレングリコール 6.0 (2)グリセリン 4.0 (3)ヒアルロン酸ナトリウム 0.1 (4)エタノール 5.0 (5)ポリオキシエチレン−オレイルエーテル(20E.O.) 0.3 (6)エデト酸二ナトリウム 0.1 (7)クエン酸ナトリウム 1.0 (8)チョウジ抽出物*11 0.2 (9)アロエ抽出物*12 0.2 (10)尿素 1.0 (11)塩化アンモニウム 0.5 (12)L−アスコルビン酸リン酸エステルマグネシウム 3.0 (13)精製水 残量 (14)防腐剤 適量 (15)香料 適量 *11 :一丸ファルコス(株)製,ファルコレックス チ
ョウジ(固形分:2.0〜4.0重量%) *12 :一丸ファルコス(株)製,アロエMS
Example 6 Lotion: A lotion having the following composition was prepared by the following method. (Composition) (% by weight) (1) 1,3-butylene glycol 6.0 (2) glycerin 4.0 (3) Sodium hyaluronate 0.1 (4) Ethanol 5.0 (5) Polyoxyethylene-oleyl Ether (20E.O.) 0.3 (6) Disodium edetate 0.1 (7) Sodium citrate 1.0 (8) Clove extract * 11 0.2 (9) Aloe extract * 12 2 (10) Urea 1.0 (11) Ammonium chloride 0.5 (12) Magnesium L-ascorbate phosphate 3.0 (13) Purified water Remaining (14) Preservatives proper amount (15) Fragrance proper amount * 11 : Ichimaru Falcos Co., Ltd., Falco Rex Chouzi (solid content: 2.0 to 4.0% by weight) * 12: Ichimaru Falcos Co., Ltd., Aloe MS

【0034】(調製方法)(1)〜(3)の成分を攪拌
分散した後、精製水(13)65部を加えAとした。一
方、(4)、(5)、(14)、(15)の成分を攪拌
溶解した後、これに残量の精製水(13)を加えBとし
た。Aを攪拌しながらBを加え均一にした後、(6)〜
(12)の成分を加え攪拌溶解した。
(Preparation method) After the components (1) to (3) were stirred and dispersed, 65 parts of purified water (13) was added to prepare A. On the other hand, after the components (4), (5), (14), and (15) were stirred and dissolved, the remaining amount of purified water (13) was added to the mixture to obtain B. After adding B while stirring A to make it uniform, (6)-
The component (12) was added and dissolved by stirring.

【0035】[0035]

【表7】 実施例5 クリーム状ファンデーション:以下にその
組成を示すクリーム状ファンデーションを下記製法によ
り調製した。 (組成) (重量%) (1)ジメチルポリシロキサン(6cs) 10.0 (2)メチルフェニルポリシロキサン 3.0 (3)オクタメチルシクロテトラシロキサン 10.0 (4)ポリオキシアルキレン変性シリコーン 5.0 (5)酸化チタン 5.0 (6)セリサイト 2.0 (7)タルク 3.0 (8)ベンガラ 0.4 (9)酸化鉄黄 0.7 (10)酸化鉄黒 0.1 (11)グリセリン 5.0 (12)オウゴン抽出物*13 0.2 (13)尿素 1.0 (14)6−アミノ−n−カプロン酸 0.5 (15)精製水 残量 (16)防腐剤 適量 (17)香料 適量 *13 :一丸ファルコス(株)製,オウゴンエキスパウダ
Example 5 Cream Foundation: A cream foundation having the following composition was prepared by the following method. (Composition) (% by weight) (1) Dimethylpolysiloxane (6cs) 10.0 (2) Methylphenylpolysiloxane 3.0 (3) Octamethylcyclotetrasiloxane 10.0 (4) Polyoxyalkylene-modified silicone 0 (5) Titanium oxide 5.0 (6) Sericite 2.0 (7) Talc 3.0 (8) Bengala 0.4 (9) Iron oxide yellow 0.7 (10) Iron oxide black 0.1 ( 11) Glycerin 5.0 (12) Agon extract * 13 0.2 (13) Urea 1.0 (14) 6-amino-n-caproic acid 0.5 (15) Purified water Remaining (16) Preservative Appropriate amount (17) Spice Appropriate amount * 13: Ougon extract powder, manufactured by Ichimaru Falcos Co., Ltd.

【0036】(調製方法)(1)〜(10)の成分を8
0℃で加熱溶解し攪拌しながら(11)〜(16)の成
分を80℃に加熱溶解した水相を加え均一に乳化した
後、(17)を加え攪拌しながら室温まで冷却した。
(Preparation method) The components (1) to (10)
An aqueous phase obtained by heating and dissolving the components (11) to (16) at 80 ° C. was added to the mixture while heating and dissolving at 0 ° C., and the mixture was uniformly emulsified.

【0037】[0037]

【表8】 実施例6 パック:以下にその組成を示すパックを下
記製法により調製した。 (組成) (重量%) (1)ジプロピレングリコール 3.0 (2)ポリエチレングリコール 3.0 (3)1,3−ブチレングリコール 1.0 (4)グリセリン 2.0 (5)ピロリドンカルボン酸ナトリウム 1.0 (6)桑白皮抽出物*14 1.5 (7)尿素 2.5 (8)乳酸 0.5 (9)乳酸ナトリウム 0.5 (10)ポリビニルアルコール 12.0 (11)エタノール 3.0 (12)ポリオキシエチレンポリオキシプロピレン デシルテトラデシルエーテル 0.3 (13)精製水 残量 (14)防腐剤 適量 (15)香料 適量 *14 :一丸ファルコス(株)製,ファルコレックス ソ
ウハクヒ(固形分:0.3〜0.8重量%)
Example 6 Pack: A pack having the following composition was prepared by the following method. (Composition) (% by weight) (1) Dipropylene glycol 3.0 (2) Polyethylene glycol 3.0 (3) 1,3-butylene glycol 1.0 (4) Glycerin 2.0 (5) Sodium pyrrolidonecarboxylate 1.0 (6) Mulberry bark extract * 14 1.5 (7) Urea 2.5 (8) Lactic acid 0.5 (9) Sodium lactate 0.5 (10) Polyvinyl alcohol 12.0 (11) Ethanol 3.0 (12) Polyoxyethylene polyoxypropylene decyl tetradecyl ether 0.3 (13) Remaining purified water (14) Appropriate amount of preservative (15) Appropriate amount of fragrance * 14: Falco Rex Souhakuhi, manufactured by Ichimaru Falcos Co., Ltd. (Solid content: 0.3-0.8% by weight)

【0038】(製法)(1)〜(9)の成分を精製水
(13)50部と攪拌溶解しAとした。(11)、(1
2)、(14)、(15)の成分を攪拌溶解した後、残
量の精製水(13)を加えて均一にしBとした。Aを攪
拌しながら(10)を加え、均一に分散した後、70℃
に加熱溶解した。これを45℃に冷却し、Bを加えて均
一にし、室温まで冷却した。
(Preparation method) The components (1) to (9) were dissolved in 50 parts of purified water (13) with stirring to give A. (11), (1
After the components (2), (14) and (15) were stirred and dissolved, the remaining amount of purified water (13) was added to make the mixture uniform and B was obtained. (10) was added while stirring A, and after uniformly dispersing,
Was heated and dissolved. This was cooled to 45 ° C., B was added to make it uniform, and it was cooled to room temperature.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI A61K 35/78 A61K 35/78 J K Q V ADA ADAC (72)発明者 鈴木 裕二 千葉県佐倉市中志津3−28−1−102 (56)参考文献 特開 昭52−79033(JP,A) 特開 昭53−88333(JP,A) 特開 平3−251514(JP,A) 特開 昭54−2344(JP,A) 特開 昭63−303910(JP,A) 特開 昭60−214721(JP,A) 特開 平3−90015(JP,A) 特開 平2−111710(JP,A) 特開 平4−282305(JP,A) 特開 平3−193713(JP,A) 特開 平4−368315(JP,A) (58)調査した分野(Int.Cl.6,DB名) A61K 7/48 A61K 7/00 A61K 35/78──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 6 Identification code FI A61K 35/78 A61K 35/78 JKQV ADA ADAC (72) Inventor Yuji Suzuki 3-28-1 Nakashitsu, Sakura City, Chiba Prefecture JP-A-52-79033 (JP, A) JP-A-53-88333 (JP, A) JP-A-3-251514 (JP, A) JP-A-54-2344 (JP, A) JP-A-63-303910 (JP, A) JP-A-60-214721 (JP, A) JP-A-3-90015 (JP, A) JP-A-2-111710 (JP, A) JP-A-4- 282305 (JP, A) JP-A-3-193713 (JP, A) JP-A-4-368315 (JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) A61K 7/48 A61K 7 / 00 A61K 35/78

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 次の成分(A)、(B)及び(C) (A)チョウジ抽出物、緑茶抽出物、葛根抽出物、桑白
皮抽出物、甘草抽出物、オウゴン抽出物、アロエ抽出物
及び橙皮抽出物から選ばれる植物抽出物の一種又は二種
以上 (B)尿素 (C)尿素安定化剤を含有することを特徴とする美白化
粧料。
1. The following components (A), (B) and (C): (A) clove extract, green tea extract, kakkon extract, mulberry bark extract, licorice extract, ogre extract, aloe extract A whitening cosmetic comprising: one or two or more plant extracts selected from an extract and an orange peel extract; (B) urea; and (C) a urea stabilizer.
JP4348612A 1992-12-28 1992-12-28 Whitening cosmetics Expired - Lifetime JP2764510B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4348612A JP2764510B2 (en) 1992-12-28 1992-12-28 Whitening cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4348612A JP2764510B2 (en) 1992-12-28 1992-12-28 Whitening cosmetics

Publications (2)

Publication Number Publication Date
JPH06199646A JPH06199646A (en) 1994-07-19
JP2764510B2 true JP2764510B2 (en) 1998-06-11

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ID=18398181

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Application Number Title Priority Date Filing Date
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Country Link
JP (1) JP2764510B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL109012A (en) * 1994-03-17 1998-09-24 Fischer Pharma Ltd Skin whitening composition comprising glycyrrhyza glabra and hydroxy acids
JP3696271B2 (en) * 1994-09-22 2005-09-14 花王株式会社 Whitening cosmetics
JPH0892055A (en) * 1994-09-22 1996-04-09 Kao Corp Whitening cosmetic
KR100516447B1 (en) * 1997-11-20 2005-12-06 주식회사 엘지생활건강 Cosmetic composition containing root extract with excellent astringent effect
GB9828380D0 (en) 1998-12-22 1999-02-17 Unilever Plc Skin lightening composition
US6248341B1 (en) 2000-01-14 2001-06-19 Color Access, Inc. Method of treating topical angiogenesis-related disorders
TWI324933B (en) * 2001-06-27 2010-05-21 Hisamitsu Pharmaceutical Co Sheet-type packs
US7435725B2 (en) 2001-11-06 2008-10-14 The Quigly Corporation Oral compositions and methods for prevention, reduction and treatment of radiation injury
FR2847267B1 (en) * 2002-11-19 2006-07-28 Coletica METHOD FOR TESTING THE ACTIVITY OF A POTENTIALLY ACTIVE SUBSTANCE FOR INHIBITING THE ENZYMATIC ACTIVITY OF A2 PHOSPHOLIPASE
JP2005075769A (en) * 2003-08-29 2005-03-24 Eiyo Kogaku Kenkyusho:Kk Pack agent for make-up
TW200808333A (en) 2006-04-17 2008-02-16 Kaneka Corp Licorice polyphenol preparation
JP2008069179A (en) * 2007-12-03 2008-03-27 Rohto Pharmaceut Co Ltd Emulsion composition
CN102648955A (en) * 2012-05-03 2012-08-29 李春仪 Skin whitening and freckle removing beautifying prescription
DE102012213935A1 (en) * 2012-08-07 2014-02-13 Beiersdorf Ag Cosmetic or dermatological preparations containing urea and containing licochalcone A or an aqueous extract of Radix Glycyrrhizae inflatae containing licochalcone A
CN105747065A (en) * 2016-03-23 2016-07-13 东莞市东卓中天生物科技有限公司 Beverage with throat-clearing and lung-clearing functions
KR102488895B1 (en) * 2020-07-30 2023-01-17 주식회사 엘지생활건강 Composition for Brightening containing sodium pyruvate

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5811922B2 (en) * 1975-12-24 1983-03-05 サンスタ−ハミガキ カブシキガイシヤ Keshiyouriyo
JPS5388333A (en) * 1977-01-13 1978-08-03 Sunstar Inc Cosmetics
JPS5948808B2 (en) * 1977-06-06 1984-11-29 サンスタ−株式会社 cosmetics
JPH03251514A (en) * 1990-02-28 1991-11-11 T Ee C Gijutsu Kagaku Kenkyusho:Kk Melanin decomposing substance

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