JPH06128137A - Cosmetic - Google Patents

Cosmetic

Info

Publication number
JPH06128137A
JPH06128137A JP27463392A JP27463392A JPH06128137A JP H06128137 A JPH06128137 A JP H06128137A JP 27463392 A JP27463392 A JP 27463392A JP 27463392 A JP27463392 A JP 27463392A JP H06128137 A JPH06128137 A JP H06128137A
Authority
JP
Japan
Prior art keywords
skin
cosmetic
effect
farnesol
pantothenol
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.)
Granted
Application number
JP27463392A
Other languages
Japanese (ja)
Other versions
JP3104938B2 (en
Inventor
Akiyoshi Matsubara
顕吉 松原
Yumi Nagasawa
由美 長澤
Masao Shaku
政雄 釈
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.)
Pola Chemical Industries Inc
Original Assignee
Pola Chemical Industries 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
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Application filed by Pola Chemical Industries Inc filed Critical Pola Chemical Industries Inc
Priority to JP04274633A priority Critical patent/JP3104938B2/en
Publication of JPH06128137A publication Critical patent/JPH06128137A/en
Application granted granted Critical
Publication of JP3104938B2 publication Critical patent/JP3104938B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To provide a cosmetic excellent in skin aging-preventive effect such as chapped skin improving effect and skin elasticity recovering effect. CONSTITUTION:The objective cosmetic formulated with (A) 0.35-14wt.% of farnesol and/or a derivative therefrom, (B) 0.15-6wt.% of pantothenol and/or a derivative therefrom and, if needed, (C) 0.000005-3wt.% of cell activator such as phytosterol glycoside, sulfated alginic acid, ethynyl estradiol, allantoin, bovine blood-freed protein, L-ascorbylmagnesium phosphate, water-soluble placenta extract, or heparin-like substance.

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、化粧料に関し、詳しく
はファルネソールとその誘導体及びパントテノールとそ
の誘導体とを含有する化粧料に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to cosmetics, and more particularly to cosmetics containing farnesol and its derivatives and pantothenol and its derivatives.

【0002】[0002]

【従来の技術】老化した皮膚は、柔軟性、弾力性を失
い、皮膚のシワが増大し乾燥した荒れ肌になることはよ
く知られている。このような皮膚の老化は、年齢と環境
によって皮膚細胞の再生が減少し、代謝活動が減少する
結果起こると言われている。
2. Description of the Related Art It is well known that aged skin loses its flexibility and elasticity, increases wrinkles on the skin, and becomes dry and rough skin. It is said that such skin aging occurs as a result of a decrease in skin cell regeneration and a decrease in metabolic activity depending on age and environment.

【0003】従来、この様な皮膚の老化を予防、改善
るために、リノール酸等の必須脂肪酸(特開昭62−3
9511号)、あるいはビタミンE(特開昭62−39
511号)等の投与が行われている。
Conventionally, in order to prevent and improve such skin aging, essential fatty acids such as linoleic acid (JP-A-62-3).
9511) or Vitamin E (JP-A-62-39).
No. 511) is being administered.

【0004】リノール酸をはじめとする必須脂肪酸が欠
乏した場合は、皮膚の落屑等が生じ著しく皮膚の老化が
促進される。これを防止するために、必須脂肪酸、ある
いはこれを含有する植物油等を化粧料に配合することが
行われているが、皮膚の老化を防止する効果は充分では
なく、又酸敗等が生じ易く、安定性に欠けるという問題
がある。
When essential fatty acids such as linoleic acid are deficient, skin desquamation and the like occur, and skin aging is significantly accelerated. In order to prevent this, essential fatty acids, or vegetable oils or the like containing them have been blended in cosmetics, but the effect of preventing skin aging is not sufficient, and rancidity and the like easily occur, There is a problem of lack of stability.

【0005】ビタミンEは、単独で用いても、湿潤作用
や老化防止効果、さらに、シワをなくす作用、キメの細
かなツヤのある美しい肌にする美肌作用はほとんど認め
られない。加えて、加熱、光で変色したり、臭気を発し
安定性がよくないという問題がある。
Even if vitamin E is used alone, almost no moisturizing action, antiaging effect, wrinkle-eliminating action, and beautiful skin-improving action for beautiful skin with fine texture are obtained. In addition, there is a problem that it is discolored by heating and light, and it emits an odor, resulting in poor stability.

【0006】[0006]

【発明が解決しようとする課題】本発明は、上記観点か
らなされたものであり、肌荒れ改善効果、シワの改善効
果、皮膚に良好な感触を与え、健常に保つ効果など、皮
膚の老化防止効果に優れた化粧料を提供することを課題
とする。
SUMMARY OF THE INVENTION The present invention has been made from the above point of view, and has an effect of preventing skin aging, such as an effect of improving rough skin, an effect of improving wrinkles, an effect of giving a good feeling to the skin and keeping it healthy. It is an object to provide excellent cosmetics.

【0007】[0007]

【課題を解決するための手段】本発明者らは、上記課題
を解決するために鋭意研究を行った結果、ファルネソー
ルとその誘導体及びパントテノールとその誘導体とを併
用すると、皮膚の老化防止効果を顕著に発揮できること
を見出し、本発明に至った。
Means for Solving the Problems As a result of intensive studies to solve the above problems, the present inventors have found that when farnesol and its derivatives and pantothenol and its derivatives are used in combination, the effect of preventing skin aging is improved. They have found that they can be remarkably exhibited, and have completed the present invention.

【0008】すなわち本発明は、ファルネソール及び/
又はその誘導体を0.35〜14重量%と、パントテノ
ール及び/又はその誘導体0.15〜6重量%とを含有
する化粧料である。
That is, the present invention provides farnesol and / or
Alternatively, it is a cosmetic containing 0.35 to 14% by weight of its derivative and 0.15 to 6% by weight of pantothenol and / or its derivative.

【0009】以下、本発明を詳細に説明する。 <1>本発明に用いる成分 (1)ファルネソールとその誘導体 ファルネソールは、植物界に広く存在する天然物であ
り、各種の精油にも含まれる。また、ファルネソール
は、経皮吸収後ステロール生合成のエレメントとなるこ
とも知られている。本発明で用いられるファルネソール
の誘導体としては、酢酸ファルネソール等が挙げられ
る。これらは、単独又は任意の組合せで使用することが
できる。
The present invention will be described in detail below. <1> Components Used in the Present Invention (1) Farnesol and its Derivatives Farnesol is a natural product widely existing in the plant kingdom and is also contained in various essential oils. Farnesol is also known to become an element of sterol biosynthesis after percutaneous absorption. Examples of the farnesol derivative used in the present invention include farnesol acetate. These can be used alone or in any combination.

【0010】(2)パントテノールとその誘導体 パントテノールは、経皮吸収後、補酵素パントテン酸に
変化し細胞の再生を増し、皮膚の水分保持能を増大させ
るといわれている。本発明で用いられるパントテノール
の誘導体とは、パンテニルエチルエーテル、三酢酸パン
トテノールエステル等が挙げられる。これらは、単独又
は任意の組合せで使用することができる。
(2) Pantothenol and its Derivatives Pantothenol is said to be converted to the coenzyme pantothenic acid after percutaneous absorption to increase cell regeneration and increase skin water retention. Examples of the pantothenol derivative used in the present invention include panthenyl ethyl ether and triacetic acid pantothenol ester. These can be used alone or in any combination.

【0011】尚、インデュケム社(Induchem
ドイツ)より、商品名ユニトリエノール T−27とし
て、ファルネソール(30%)、酢酸ファルネソール
(40%)、三酢酸パントテノールエステル(30%)
の混合物が市販されており、これを、ファルネソール及
びパントテノールあるいはこれらの誘導体の混合物とし
てそのまま使用することもできる。
Induchem (Induchem)
(Germany) under the trade name Unitrienol T-27, Farnesol (30%), Farnesol acetate (40%), Pantothenol triacetate (30%)
Is commercially available and can be used as it is as a mixture of farnesol and pantothenol or their derivatives.

【0012】(3)細胞賦活剤 上記ファルネソール及びパントテノールあるいはこれら
の誘導体と共に、細胞賦活剤を併用することにより、皮
膚の老化防止効果を一層高めることができる。このよう
な細胞賦活剤としては、フィトステロール配糖体、硫酸
化アルギン酸、エチニルエストラジオール、アラントイ
ン、牛血液除タンパク物、リン酸L−アスコルビルマグ
ネシウム、水溶性プラセンタエキス、ヘパリン類似物質
等が挙げられ、これらのうち一種、あるいは任意の2種
以上の混合物として使用できる。
(3) Cell activating agent By using a cell activating agent together with the above farnesol and pantothenol or their derivatives, the effect of preventing skin aging can be further enhanced. Examples of such cell activating agents include phytosterol glycosides, sulfated alginic acid, ethinyl estradiol, allantoin, bovine blood deproteinization products, L-ascorbyl magnesium phosphate, water-soluble placenta extract, and heparin-like substances. They can be used as one kind or a mixture of two or more kinds.

【0013】フィトステロール配糖体は、特開昭62−
72604号公報、特開昭62−187404号公報
に、牛血液除タンパク物は、特公昭48−23908号
公報に、硫酸化アルギン酸は、特開昭4−257509
号公報に詳述されている。記載されている。
Phytosterol glycosides are disclosed in JP-A-62-
72604 and JP-A-62-187404, bovine blood deproteinized protein is disclosed in JP-B-48-23908, and sulfated alginic acid is disclosed in JP-A-4-257509.
It is described in detail in the publication. Have been described.

【0014】エチニルエストラジオール、アラントイン
は、化粧料に広く用いられているものであり、化粧品原
料基準に収載されている。リン酸L−アスコルビルマグ
ネシウム、水溶性プラセンタエキスは、いずれも化粧品
に広く用いられているものであり、化粧品種別許可基準
(厚生省薬務局審査第2課監修)V、IIに各々収載され
ている。
Ethynyl estradiol and allantoin are widely used in cosmetics and are listed in the standard of cosmetic raw materials. L-ascorbyl magnesium phosphate and water-soluble placenta extract are widely used in cosmetics, and are listed in the cosmetic product type permission standards (supervised by the Ministry of Health and Welfare Pharmaceutical Affairs Bureau Examination 2nd Division) V and II, respectively. .

【0015】ヘパリン類似物質は、主として、牛の気管
軟骨を含む肺臓から抽出したムコ多糖の多硫酸エステル
であり、日本薬局方外医薬品成分規格1983(厚生省
薬務局審査課監修)に収載されている。
The heparin-like substance is mainly a polysulfate ester of mucopolysaccharide extracted from the lung containing bovine tracheal cartilage, and is listed in the Japanese Pharmacopoeia Standard for Pharmaceutical Ingredients 1983 (supervised by the Examination Division, Pharmaceutical Affairs Bureau, Ministry of Health and Welfare). There is.

【0016】<2>本発明の化粧料 本発明の化粧料は、上記ファルネソール及び/又はその
誘導体と、パントテノール及び/又はその誘導体を必須
成分として含有するものである。さらに、上記細胞賦活
剤を併用してもよい。
<2> Cosmetic of the Present Invention The cosmetic of the present invention contains the above farnesol and / or its derivative and pantothenol and / or its derivative as essential components. Furthermore, you may use together said cell activator.

【0017】ファルネソール及び又はその誘導体の配合
量は、化粧料全量に対し0.35〜14重量%が好まし
い。0.35重量%より少量では、充分な効果が得られ
ない。また、14重量%を越えると、安全性に問題が生
じたり、化粧品系を安定に保つことが困難になる。
The blending amount of farnesol and / or its derivative is preferably 0.35 to 14% by weight with respect to the total amount of the cosmetic. If it is less than 0.35% by weight, a sufficient effect cannot be obtained. On the other hand, when it exceeds 14% by weight, safety problems occur and it becomes difficult to keep the cosmetic system stable.

【0018】パントテノール及び/又はその誘導体の配
合量は、化粧料全量に対し0.15〜6重量%が好まし
い。0.15重量%より少量では、充分な効果が得られ
ない。また、6重量%を越えると、安全性に問題が生じ
たり、化粧品系を安定に保つことが困難になる。
The blending amount of pantothenol and / or its derivative is preferably 0.15 to 6% by weight based on the total amount of the cosmetic. If it is less than 0.15% by weight, a sufficient effect cannot be obtained. On the other hand, if it exceeds 6% by weight, safety problems occur and it becomes difficult to keep the cosmetic system stable.

【0019】細胞賦活剤を併用する場合には、化粧料全
量に対し0.000005〜3重量%が好ましい。0.
000005重量%より少量では、十分な効果が得られ
ない。3重量%を越えると、変色、変臭するなど安定性
や安全性上好ましくない。
When a cell activator is used in combination, the amount is preferably 0.000005 to 3% by weight based on the total amount of the cosmetic. 0.
If the amount is less than 000005% by weight, a sufficient effect cannot be obtained. If it exceeds 3% by weight, discoloration or odor will occur, which is not preferable in terms of stability and safety.

【0020】本発明の化粧料は、特に剤型は問わず、化
粧水、クリーム、乳液、パックなどに直接添加するか、
あるいはアルコール類などの溶剤(例えばエタノール)
に溶解したものを添加配合して乳化、混合、分解、溶解
等の処理を行うことによって得られる。
The cosmetic of the present invention may be added directly to a lotion, cream, emulsion, pack or the like, regardless of the dosage form.
Or solvents such as alcohols (eg ethanol)
It can be obtained by adding and blending what is dissolved in and performing treatments such as emulsification, mixing, decomposition and dissolution.

【0021】また、本発明の化粧料には、上記成分の
他、通常の化粧料に用いられる各種の化粧品用基剤及び
添加物、例えば無機顔料、有機顔料、無機粉体、有機粉
体、炭化水素類、シリコーン類、エステル類、トリグリ
セリド類、ラノリン類、ワックス類、ロウ類、動植物
油、界面活性剤、多価アルコール類などの基剤や糖類、
ビタミンA、ビタミンB群、ビタミンEなどのビタミン
類、アミノ酸類、グリチルリチンやその誘導体あるいは
グリチルレチン酸やその誘導体などの抗炎症剤、酸化防
止剤、防腐剤、香料、増粘剤、収斂剤、紫外線吸収剤、
紫外線反射剤、美白剤、肌荒れ改善剤等の添加物を配合
することができる。
In the cosmetic of the present invention, in addition to the above components, various cosmetic bases and additives used in ordinary cosmetics, such as inorganic pigments, organic pigments, inorganic powders, organic powders, Bases and sugars such as hydrocarbons, silicones, esters, triglycerides, lanolins, waxes, waxes, animal and vegetable oils, surfactants, polyhydric alcohols, etc.,
Vitamin A, B vitamins, vitamins such as vitamin E, amino acids, glycyrrhizin and its derivatives, anti-inflammatory agents such as glycyrrhetinic acid and its derivatives, antioxidants, preservatives, perfumes, thickeners, astringents, ultraviolet rays Absorbent,
Additives such as a UV-reflecting agent, a whitening agent, and a rough skin improving agent can be added.

【0022】[0022]

【実施例】以下に、本発明の実施例を説明する。尚、以
下の配合量は全て重量部である。
EXAMPLES Examples of the present invention will be described below. In addition, the following compounding amounts are all parts by weight.

【0023】[0023]

【実施例1〜8】本発明の化粧料として、クリームにお
ける実施例を説明する。 (製法)表1A、Bの成分を75℃に加熱し、溶解させ
た後、Aの成分にBの成分を加え、反転乳化した。これ
を30℃まで冷却し、実施例1〜8及び比較例1の水中
油型クリームを得た。
Examples 1 to 8 Examples of creams as the cosmetics of the present invention will be described. (Manufacturing method) The components of Table 1A and B were heated to 75 ° C. to dissolve them, and then the component of B was added to the component of A to perform inversion emulsion. This was cooled to 30 ° C. to obtain oil-in-water creams of Examples 1-8 and Comparative Example 1.

【0024】[0024]

【表1】 (評価)次に、上記各クリームの効果を検討するため、
使用テスト、肌荒れ改善効果テスト及び角層剥離状態改
善効果テスト、シワ改善効果テストを行った。
[Table 1] (Evaluation) Next, in order to examine the effect of each cream,
A use test, a rough skin improving effect test, a stratum corneum peeling state improving effect test, and a wrinkle improving effect test were performed.

【0025】<1>使用テスト (方法)50名の女子パネラー(35〜49歳)の顔面
に、上記実施例及び比較例のクリームを、1日2回、1
カ月間連続塗布し、試験開始前及び終了後の皮膚の状態
をパネラー本人が官能評価を行った。尚、評価項目は、
表2に示す5項目とし、各々3段階で評価した。結果を
表2に示す。
<1> Use Test (Method) The creams of the above-mentioned Examples and Comparative Examples were applied to the face of 50 female panelists (35-49 years old) twice a day for 1 day.
After continuous application for a month, the panelist himself performed sensory evaluation on the skin condition before and after the test. The evaluation items are
Five items shown in Table 2 were used, and each item was evaluated in three stages. The results are shown in Table 2.

【0026】[0026]

【表2】 この結果から、実施例のクリームは、比較例のクリーム
に比べ、肌をしっとりさせ、肌のカサつきをなくす効
果、さらに、肌を健常に保ち、小ジワを減少させる効果
に優れていることがわかる。
[Table 2] From these results, the cream of Example is superior to the cream of Comparative Example in the effect of moisturizing the skin, eliminating the dryness of the skin, and further keeping the skin healthy and reducing fine lines. Recognize.

【0027】<2>肌荒れ改善効果テスト及び角層剥離
状態改善効果テスト 前腕の荒れ肌を有する中高年50名を対象として、1日
2回、1カ月間、実施例1、2、5あるいは比較例1の
クリームの連続塗布を行い、肌荒れ改善効果テスト及び
角層剥離状態改善効果テストを行った。
<2> Skin roughening improving effect test and stratum corneum peeling state improving effect test Targeting 50 middle-aged and elderly people with rough skin on the forearm, twice a day for one month, Examples 1, 2, 5 or Comparative Example 1 Was continuously applied, and a rough skin improving effect test and a stratum corneum peeling condition improving effect test were performed.

【0028】(1)肌荒れ改善効果テスト (実験方法)試験開始前及び終了後の皮膚の状態を下記
の基準により判定し、試験前後の試験部位との対照部位
の判定結果を比較し、皮膚乾燥度が2段階以上改善され
た場合(例えば+→−、++→±)を「有効」、1段階
改善された場合を「やや有効」、変化がなかった場合を
「無効」とした。尚、試験期間中に皮膚の乾燥が進んだ
例はなかった。
(1) Skin Roughness Improvement Effect Test (Experimental Method) The condition of the skin before and after the test is judged according to the following criteria, and the judgment results of the test site before and after the test and the control site are compared to dry skin When the degree was improved by two stages or more (for example, + → −, ++ → ±), it was defined as “valid”, when it was improved by 1 stage, it was defined as “slightly valid”, and when there was no change, it was defined as “invalid”. Incidentally, there was no case where the skin became dry during the test period.

【0029】− : 正常 ± : 軽微乾燥、落屑なし + : 乾燥、落屑軽度 ++ : 乾燥、落屑中等度 +++: 乾燥、落屑顕著-: Normal ±: Minor dryness, no desquamation +: Dry, mild desquamation ++: Dry, moderate desquamation +++: Dry, remarkable desquamation

【0030】(2)角層剥離状態の改善効果テスト セロファンテープを用いて角層を採取し、アルコール中
に10分漬け、その後染色液(1%ゲンチアナバイオレ
ット:0.5%ブリリアントグリーン水溶液)に約10
〜15分間浸漬させた後、染色液が出なくなるまで流水
に浸漬し、ドライヤーで風燥させた。その後、染色され
た角層細胞をバルサム液で封入し、顕微鏡にて観察し、
3段階で評価した。
(2) Test for improving effect of exfoliation of stratum corneum The stratum corneum was sampled using cellophane tape, soaked in alcohol for 10 minutes, and then applied to a dyeing solution (1% gentian violet: 0.5% brilliant green aqueous solution). About 10
After soaking for -15 minutes, it was soaked in running water until no dyeing solution came out, and dried with a dryer. Then, the stained corneal cells are sealed with balsam solution and observed under a microscope.
The evaluation was made in 3 stages.

【0031】以上のテストの結果を表3に示す。The results of the above tests are shown in Table 3.

【0032】[0032]

【表3】 [Table 3]

【0033】<3>シワ改善テスト 次に、シワ改善テストを行った。 (方法)30名の中年(35〜49才)女子パネラーの
顔面に、実施例1、4、5あるいは比較例1のクリーム
を1日2回塗布し、1カ月後、本人が試験開始前及び終
了後の皮膚に対する状態について、表4に示した3項目
を評価した。尚、しわ改善効果は以下のようにして評価
した。
<3> Wrinkle Improvement Test Next, a wrinkle improvement test was conducted. (Method) The cream of Examples 1, 4, 5 or Comparative Example 1 was applied twice a day to the faces of 30 middle-aged (35-49 years old) female panelists, and one month later, before the start of the test. And, regarding the condition on the skin after the end, the three items shown in Table 4 were evaluated. The effect of improving wrinkles was evaluated as follows.

【0034】皮膚より採取したシリコンレプリカをガラ
ス板に固定し、レプリカに対して斜め方向(25度)か
ら平行光線を照射した。それを真上からTVカメラで撮
影すると、レプリカの凸凹に応じた陰影により、凸部は
明るく、凹部は暗く撮影される。この明るさを輝度値に
変換し、Ra(平均粗さ)、波形、Sm値(皮溝間距
離)を求めた。また、レプリカ写真の肉眼判定を同時に
行い、シワ改善効果を評価した。以上の結果を表4に示
す。
The silicon replica collected from the skin was fixed on a glass plate, and parallel rays were irradiated to the replica from an oblique direction (25 degrees). When it is photographed from directly above with a TV camera, the convex portions are bright and the concave portions are dark due to the shadows corresponding to the irregularities of the replica. This brightness was converted into a luminance value, and Ra (average roughness), waveform, and Sm value (distance between skin grooves) were obtained. In addition, the naked eye judgment of the replica photograph was performed at the same time to evaluate the wrinkle reducing effect. The above results are shown in Table 4.

【0035】[0035]

【表4】 この結果から、本発明のクリームは、シワ改善効果に優
れていることがわかる。
[Table 4] From this result, it is understood that the cream of the present invention is excellent in the wrinkle reducing effect.

【0036】[0036]

【実施例9】次に、本発明の化粧料として、化粧水にお
ける実施例を説明する。 (製法)表5に示した成分全量を、室温にて均質に混合
溶解して化粧水を得た。
[Embodiment 9] Next, as a cosmetic of the present invention, an embodiment in a lotion will be described. (Manufacturing method) All the ingredients shown in Table 5 were homogeneously mixed and dissolved at room temperature to obtain a lotion.

【0037】[0037]

【表5】 [Table 5]

【0038】[0038]

【実施例10】本発明の化粧料として、乳液における実
施例を説明する。 (製法)表6A、Bの各成分を各々75℃に加熱し、溶
解した。この後、AにBを加え、反転乳化した後、30
℃まで冷却し、水中油型乳液を得た。
[Embodiment 10] As a cosmetic of the present invention, an embodiment in an emulsion will be described. (Manufacturing Method) Each of the components shown in Tables 6A and 6B was heated to 75 ° C. and dissolved. After this, B was added to A, and the emulsion was inverted.
It cooled to 0 degreeC and obtained the oil-in-water type emulsion.

【0039】[0039]

【表6】 [Table 6]

【0040】[0040]

【実施例11】さらに、パック料における実施例を説明
する。 (製法)表7の成分全量を室温にて均質に混合溶解して
パックを得た。
[Embodiment 11] Further, an embodiment of the pack charge will be described. (Manufacturing method) All the components shown in Table 7 were homogeneously mixed and dissolved at room temperature to obtain a pack.

【0041】[0041]

【表7】 [Table 7]

【0042】[0042]

【発明の効果】本発明の化粧料は、肌荒れ改善効果、シ
ワの改善効果、皮膚に良好な感触を与え、健常に保つ効
果など、皮膚の老化防止効果に優れている。
The cosmetics of the present invention are excellent in the effect of preventing skin aging, such as the effect of improving skin roughness, the effect of improving wrinkles, the effect of giving a good feel to the skin, and the effect of keeping them healthy.

フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 A61K 7/00 K 7252−4C W 7252−4C H 7252−4C Continuation of front page (51) Int.Cl. 5 Identification number Office reference number FI Technical display location A61K 7/00 K 7252-4C W 7252-4C H 7252-4C

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 ファルネソール及び/又はその誘導体を
0.35〜14重量%と、パントテノール及び/又はそ
の誘導体0.15〜6重量%とを含有する化粧料。
1. A cosmetic containing farnesol and / or a derivative thereof in an amount of 0.35 to 14% by weight and pantothenol and / or a derivative thereof in an amount of 0.15 to 6% by weight.
【請求項2】 さらに、細胞賦活剤を0.000005
〜3重量%含有する請求項1記載の化粧料。
2. A cell activating agent is further added in an amount of 0.000005.
The cosmetic according to claim 1, wherein the cosmetic is contained in an amount of 3 wt%.
【請求項3】 前記細胞賦活剤が、フィトステロール配
糖体、硫酸化アルギン酸、エチニルエストラジオール、
アラントイン、牛血液除タンパク物、リン酸L−アスコ
ルビルマグネシウム、水溶性プラセンタエキス、ヘパリ
ン類似物質からなる群より選ばれることを特徴とする請
求項1又は2記載の化粧料。
3. The cell activating agent is phytosterol glycoside, sulfated alginic acid, ethinyl estradiol,
The cosmetic according to claim 1 or 2, wherein the cosmetic is selected from the group consisting of allantoin, bovine blood deproteinate, magnesium L-ascorbyl phosphate, water-soluble placenta extract, and heparin-like substance.
JP04274633A 1992-10-13 1992-10-13 Cosmetics Expired - Lifetime JP3104938B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP04274633A JP3104938B2 (en) 1992-10-13 1992-10-13 Cosmetics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP04274633A JP3104938B2 (en) 1992-10-13 1992-10-13 Cosmetics

Publications (2)

Publication Number Publication Date
JPH06128137A true JPH06128137A (en) 1994-05-10
JP3104938B2 JP3104938B2 (en) 2000-10-30

Family

ID=17544428

Family Applications (1)

Application Number Title Priority Date Filing Date
JP04274633A Expired - Lifetime JP3104938B2 (en) 1992-10-13 1992-10-13 Cosmetics

Country Status (1)

Country Link
JP (1) JP3104938B2 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000069404A1 (en) * 1999-05-17 2000-11-23 The Procter & Gamble Company Methods for regulating the condition of mammalian keratinous tissue via topical application of phytosterol compositions
WO2001013881A1 (en) * 1999-08-24 2001-03-01 Kao Corporation Cosmetics
WO2000062742A3 (en) * 1999-04-19 2001-05-17 Procter & Gamble Methods for regulating the condition of mammalian keratinous tissue
US6444647B1 (en) 1999-04-19 2002-09-03 The Procter & Gamble Company Skin care compositions containing combination of skin care actives
KR100461761B1 (en) * 2002-04-18 2004-12-14 주식회사 태평양 Composition for external application to the skin and anti-xerosis agent containing Farnesol
JP2005501063A (en) * 2001-08-10 2005-01-13 ザ プロクター アンド ギャンブル カンパニー Topical leave-on composition containing selected pantothenic acid derivatives

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000062742A3 (en) * 1999-04-19 2001-05-17 Procter & Gamble Methods for regulating the condition of mammalian keratinous tissue
US6284802B1 (en) 1999-04-19 2001-09-04 The Procter & Gamble Company Methods for regulating the condition of mammalian keratinous tissue
US6444647B1 (en) 1999-04-19 2002-09-03 The Procter & Gamble Company Skin care compositions containing combination of skin care actives
WO2000069404A1 (en) * 1999-05-17 2000-11-23 The Procter & Gamble Company Methods for regulating the condition of mammalian keratinous tissue via topical application of phytosterol compositions
WO2001013881A1 (en) * 1999-08-24 2001-03-01 Kao Corporation Cosmetics
JP2005501063A (en) * 2001-08-10 2005-01-13 ザ プロクター アンド ギャンブル カンパニー Topical leave-on composition containing selected pantothenic acid derivatives
KR100461761B1 (en) * 2002-04-18 2004-12-14 주식회사 태평양 Composition for external application to the skin and anti-xerosis agent containing Farnesol

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