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JPH0733637A - Skin cosmetic - Google Patents

Skin cosmetic

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Publication number
JPH0733637A
JPH0733637A JP20045093A JP20045093A JPH0733637A JP H0733637 A JPH0733637 A JP H0733637A JP 20045093 A JP20045093 A JP 20045093A JP 20045093 A JP20045093 A JP 20045093A JP H0733637 A JPH0733637 A JP H0733637A
Authority
JP
Japan
Prior art keywords
skin
effect
test
improving
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.)
Pending
Application number
JP20045093A
Other languages
Japanese (ja)
Inventor
Akinori Haratake
昭憲 原武
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.)
Kanebo Ltd
Original Assignee
Kanebo Ltd
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 Kanebo Ltd filed Critical Kanebo Ltd
Priority to JP20045093A priority Critical patent/JPH0733637A/en
Publication of JPH0733637A publication Critical patent/JPH0733637A/en
Pending legal-status Critical Current

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  • Cosmetics (AREA)

Abstract

PURPOSE:To obtain a skin cosmetic excellent in preventing effects on skin (improving effects on roughened skin and a horny substance and accelerating effects on the turnover of a horny layer, skin beautifying effects, etc.). CONSTITUTION:This skin cosmetic is obtained by blending an epidermal growth factor with at least one selected from ceramides, cerebrosides, cholesterol and phospholipids.

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、老化皮膚改善効果(荒
れ肌改善効果、角質改善効果、角質層のタ−ンオ−バ−
を速くする効果、美肌効果等)の優れた皮膚化粧料に関
する。
FIELD OF THE INVENTION The present invention relates to an effect of improving aged skin (effect of improving rough skin, effect of improving keratin, turnover of horny layer).
The present invention relates to a skin cosmetic having an excellent effect of speeding up the skin, a beautiful skin effect, etc.).

【0002】[0002]

【従来の技術】老化皮膚とは、乾燥した滑らかさのない
荒れ肌で、角質細胞の剥離現象が認められ、結合組織は
コラ−ゲン/エラスチン比が高く、しわが多い皮膚をい
う。一方、老化皮膚は細胞代謝の低下により角質層のタ
−ンオ−バ−が遅い。その改善のため、皮膚に老化防止
成分を付与するとタ−ンオ−バ−が速くなると一般に言
われており、種々の皮膚組織賦活成分が研究されてい
る。その中でも、上皮成長因子(Eidermal G
rowth Factor、以下EGFと略記する)
は、培養細胞を用いた実験により、表皮細胞の分化を促
進し、細胞の寿命を延ばし、さらに皮膚線維芽細胞の増
殖を促進させることが知られている。
BACKGROUND OF THE INVENTION Aged skin is dry and non-smooth rough skin in which exfoliation of keratinocytes is observed and the connective tissue has a high collagen / elastin ratio and wrinkles. On the other hand, in aged skin, the turnover of the stratum corneum is slow due to a decrease in cell metabolism. In order to improve it, it is generally said that the turnover becomes faster when an antiaging component is added to the skin, and various skin tissue activating components have been studied. Among them, epidermal growth factor (Eidermal G)
(rowth Factor, hereinafter abbreviated as EGF))
Is known to promote differentiation of epidermal cells, prolong cell life, and promote proliferation of skin fibroblasts by experiments using cultured cells.

【0003】最近、皮膚老化防止効果を持つ化粧料とし
て、EGFを配合した化粧料または皮膚用剤が提案され
ている(特開昭60−258105号公報、特開昭61
−5006号公報)。しかし、これらを詳細に検討する
と充分な効果が得られないことが判明した。実用上、皮
膚の組織機能を修復または改善し、これにより皮膚が元
来保有する機能を回復させる様な皮膚の老化防止に著効
を示す、優れた皮膚化粧料を得ることは困難であった。
Recently, as a cosmetic having an effect of preventing skin aging, a cosmetic or a dermatological agent containing EGF has been proposed (JP-A-60-258105 and JP-A-61).
-5006). However, it was revealed that sufficient effects could not be obtained when these were examined in detail. Practically, it was difficult to obtain an excellent skin cosmetic which is effective in preventing aging of the skin by repairing or improving the tissue function of the skin and thereby restoring the function originally possessed by the skin. .

【0004】[0004]

【発明が解決しようとする課題】そこで、本発明者は、
上記の事情に鑑み鋭意研究した結果、後記皮膚化粧料が
老化皮膚改善効果(荒れ肌改善効果、角質改善効果、角
質層のタ−ンオ−バ−を速くする効果、美肌効果等)に
優れることを確認して本発明を完成するに至った。
Therefore, the inventor of the present invention
As a result of intensive studies in view of the above circumstances, it is shown that the skin cosmetics described below are excellent in the effect of improving aging skin (effect of improving rough skin, effect of improving keratin, effect of accelerating turnover of horny layer, effect of beautiful skin, etc.). After confirmation, the present invention was completed.

【0005】すなわち、本発明の目的とするところは、
皮膚老化防止効果(荒れ肌改善効果、角質改善効果、角
質層のタ−ンオ−バ−を速くする効果、美肌効果等)の
優れた皮膚化粧料を提供することにある。
That is, the object of the present invention is to
It is an object of the present invention to provide a skin cosmetic excellent in the effect of preventing skin aging (effect of improving rough skin, effect of improving keratin, effect of accelerating turnover of stratum corneum, effect of beautiful skin, etc.).

【0006】[0006]

【課題を解決するための手段】上述の目的は、EGF
と、セラミド、セレブロシド、コレステロ−ルおよびリ
ン脂質より選択された少なくとも1つとを配合すること
を特徴とする皮膚化粧料によって達成される。
The above-mentioned object is to achieve the EGF.
And at least one selected from ceramide, cerebroside, cholesterol and phospholipid.

【0007】本発明に使用するEGFは、ヒトやマウス
等の動物由来の組織、乳汁、唾液、血液、尿等から、あ
るいは微生物(大腸菌等)による醗酵生産物から、抽出
精製することにより得られるペプチドの一種であり、前
記特開昭60−258105号公報、特開昭61−50
06号公報に示された方法によって得られる。
The EGF used in the present invention can be obtained by extraction and purification from tissues derived from animals such as humans and mice, milk, saliva, blood, urine or the like, or from fermentation products of microorganisms such as Escherichia coli. It is a kind of peptide and is disclosed in the above-mentioned JP-A-60-258105 and JP-A-61-50.
It is obtained by the method disclosed in Japanese Patent Laid-Open No. 06.

【0008】セラミド、セレブロシド、コレステロ−ル
およびリン脂質(角質細胞間脂質)は表皮角質層の細胞
間に存在して保水作用を示すことが知られている。これ
らは、動物由来の組織、乳汁、血液等から抽出精製する
か、または人工的に化学合成することにより得られる。
なお、リン脂質としてはジアシルホスファチジルコリ
ン、ジアシルホスファチジルエタノールアミン、ジアシ
ルホスファチジルイノシトール、ジアシルホスファチジ
ルセリンおよびそれらのリゾ体が挙げられる。
Ceramide, cerebroside, cholesterol and phospholipid (intercorneal lipid) are known to exist between cells of the stratum corneum of the epidermis and show a water retaining effect. These are obtained by extraction and purification from animal-derived tissues, milk, blood or the like, or by artificial chemical synthesis.
Examples of phospholipids include diacylphosphatidylcholine, diacylphosphatidylethanolamine, diacylphosphatidylinositol, diacylphosphatidylserine and their lyso forms.

【0009】本発明のEGFと、セラミド、セレブロシ
ド、コレステロ−ルおよびリン脂質より選択された少な
くとも1つとを配合してなる皮膚化粧料は、これらの相
乗効果によって表皮細胞の増殖および分化を顕著に促進
して皮膚機能を亢進する。また、角質層の保水効果も著
しく向上し、皮膚が本来備えている機能を修復或いは改
善して皮膚を健常な状態に保持し、特に老化皮膚に適用
する場合、顕著な効果が認められた。それらの作用は、
これらの単独の場合のそれからは予想されないものであ
った。
A skin cosmetic composition comprising the EGF of the present invention and at least one selected from ceramide, cerebroside, cholesterol and phospholipid has a prominent effect on the proliferation and differentiation of epidermal cells due to their synergistic effect. Promotes and enhances skin function. Further, the water-retaining effect of the stratum corneum was remarkably improved, and the function originally possessed by the skin was restored or improved to maintain the skin in a healthy state, and particularly when applied to aged skin, a remarkable effect was observed. Their action is
It was not expected from those alone.

【0010】EGFの配合量は、皮膚化粧料の総量を基
準として0.0001〜1.0重量%、角質細胞間脂質
の配合料は同様に0.01〜5.0重量%が好ましい。
これら各々の下限未満の配合量では、本発明の目的とす
る効果が少なく、一方、上限を越えてもその増加分に見
合った効果の向上は得られにくい。
The EGF content is preferably 0.0001 to 1.0% by weight, and the intercorneocyte lipid content is preferably 0.01 to 5.0% by weight, based on the total amount of the skin cosmetic.
If the compounding amount is less than the lower limit of each of these, the effect aimed at by the present invention is small, while if it exceeds the upper limit, it is difficult to obtain the effect corresponding to the increase.

【0011】本発明の皮膚化粧料は、例えばロ−ション
類、乳液類、クリ−ム類、パック類等に適用することが
できる。尚、本発明の皮膚化粧料には上記の他に色素、
香料、防腐剤、界面活性剤、顔料、抗酸化剤等を本発明
の目的を達成する範囲内で適宜配合することができる。
The skin cosmetic of the present invention can be applied to lotions, emulsions, creams, packs and the like. In addition to the above, the skin cosmetic of the present invention contains a pigment,
Fragrances, preservatives, surfactants, pigments, antioxidants and the like can be appropriately added within a range that achieves the object of the present invention.

【0012】[0012]

【実施例】以下、実施例および比較例に基づいて本発明
を詳説する。
EXAMPLES The present invention will be described in detail below based on examples and comparative examples.

【0013】実施例1〜5および比較例1〜6 荒れ肌効果試験、角質改善効果試験、角質層のタ−ンオ
−バ−測定試験、官能テスト(美肌効果試験)の試験方
法について記載する。
Examples 1 to 5 and Comparative Examples 1 to 6 The test methods of the rough skin effect test, the keratin improvement effect test, the turnover measurement test of the stratum corneum, and the sensory test (beautiful skin effect test) will be described.

【0014】荒れ肌改善効果試験 下脚部に荒れ肌を有する中高年被験者10名を対象とし
て試料を4週間連続塗布し、その効果を調べた。すなわ
ち、被験者の左側下脚外側試験部位に1日1回約0.5
gの試料を塗布し、試験開始前および終了後の皮膚の状
態を表1の判定基準により判定した。右側下脚部は試料
を塗布せず対照とした。
Rough skin improvement effect test A sample was applied continuously to 10 middle-aged and elderly subjects who have rough skin on the lower legs for 4 weeks, and the effect was examined. That is, about 0.5 per once a day on the test site on the left lower leg of the subject.
g of the sample was applied, and the condition of the skin before and after the start of the test was evaluated according to the criteria shown in Table 1. The lower right leg was not coated with the sample and served as a control.

【0015】[0015]

【表1】 [Table 1]

【0016】試験前後の試験部位と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。試験結
果は有効、やや有効となった被験者の人数で示した。
The judgment results of the test site before and after the test and the control site are compared, and when the skin dryness is improved by two stages or more (for example, + →-, ++ → ±), it is effective when one stage is improved. Valid, invalid when there was no change. The test results were shown by the number of subjects who were valid or slightly valid.

【0017】角質改善(角質細胞の抗剥離性増大)効
果試験 前述の荒れ肌改善効果試験開始前および終了後の被験部
皮膚にスコッチテ−プ(ニチバンメンデイングテ−プ)
を接着し、これを剥離した時テ−プに付着した角質細胞
の状態を走査型電子顕微鏡によって詳細に調べ、表2の
基準によって皮膚角質細胞抗剥離性を解析し、角質改善
効果を求めた。
Test for effect of improving keratin (increasing anti-peeling property of keratinocytes) Scotch tape (Nichiban Mending Tape) on the skin of the test area before and after the start of the test for improving rough skin described above.
Was inspected and the state of keratinocytes attached to the tape when peeled off was examined in detail by a scanning electron microscope, and the anti-peelability of skin keratinocytes was analyzed according to the criteria in Table 2 to determine the keratin improving effect. .

【0018】[0018]

【表2】 [Table 2]

【0019】評価は4週間連続塗布後の試験部位の評価
点と対照部位のそれとの差が2点以上改善された場合を
有効、1点の場合をやや有効、0点の場合を無効とし
た。判定結果は有効、やや有効となった被験者の人数で
示した。
The evaluation was made effective when the difference between the evaluation point of the test site and that of the control site after continuous application for 4 weeks was improved by 2 points or more, 1 case was slightly effective, and 0 point was invalid. . The judgment results are shown by the number of subjects who were valid and slightly valid.

【0020】角質層のタ−ンオ−バ−測定試験 蛍光色素のダンシルクロライドを白色ワセリン中に5重
量%配合した軟膏を作り、被験者10名の前腕部の皮膚
に24時間閉塞貼布し、角質層にダンシルクロライドを
浸透結合させる。その後、同じ部位に1日2回(朝・
夕)被験試料を約0.2g塗布し、毎日1回暗所で紫外
線Aランプを用いて、ダンシルクロライドの蛍光を調
べ、その蛍光が消滅するまでの日数を皮膚角質層のタ−
ンオ−バ−とした。
Turnover measurement test of the stratum corneum An ointment was prepared by mixing 5% by weight of the fluorescent dye dansyl chloride in white petrolatum, and applied on the skin of the forearm of 10 test subjects for 24 hours, and keratinized. Permeabilize the layers with dansyl chloride. After that, on the same site twice a day (morning
Evening) Approximately 0.2 g of the test sample was applied, and once a day, the fluorescence of dansyl chloride was examined by using an ultraviolet A lamp in the dark, and the number of days until the fluorescence disappeared was measured as the number of days until the fluorescence disappeared.
It was overloaded.

【0021】測定結果は各被験者の日数の平均値で示し
た。なお、通常の皮膚角質層のタ−ンオ−バ−は12〜
15日であるが、老化した皮膚においては18日前後に
のびる。それに対して老化防止効果が現れると12日程
度にまで短縮される。
The measurement results are shown by the average value of the number of days of each subject. Normal turnover of stratum corneum is 12-
Although it is 15 days, it spreads around 18 days in aged skin. On the other hand, when the anti-aging effect appears, it is shortened to about 12 days.

【0022】官能テスト(美肌効果試験) 荒れ肌、小じわ、乾燥肌等を訴える女子被験者(35〜
55才)10人に試料を1日2回(朝・夕)連続3ケ月
塗布して3ケ月後の効果を評価した。試験結果は、皮膚
の湿潤性、平滑性、弾力性の各項目に対して、皮膚に潤
いが生じた、皮膚が滑らかになった、皮膚に張りが生じ
たと回答した人数で示した。
Sensory test (Beautiful skin effect test) Female subjects who complain of rough skin, fine wrinkles, dry skin (35-35)
The sample was applied to 10 people (55 years old) twice a day (morning and evening) for 3 consecutive months, and the effect after 3 months was evaluated. The test results are shown by the number of people who responded that moisturized skin, smoothed skin, and tense skin were generated for each item of wettability, smoothness, and elasticity of the skin.

【0023】[スキンロ−ション]表3に示した組成の
スキンロ−ション基剤にEGF、セラミド、セレブロシ
ド、コレステロ−ル、リン脂質を表4に記載の通りに配
合して各々のスキンロ−ションを調製し、前記諸試験を
実施した。
[Skin lotion] EGF, ceramide, cerebroside, cholesterol and phospholipid were added to the skin lotion base having the composition shown in Table 3 as shown in Table 4 to obtain each skin lotion. It prepared and the said various tests were implemented.

【0024】組成Composition

【表3】 [Table 3]

【0025】調製法 C成分のEGFはB成分に、D成分のセラミド、セレブ
ロシド、コレステロ−ル、リン脂質はA成分に配合し
て、A、B成分を均一に溶解した後、A成分とB成分を
混合攪拌分散し、次いで容器に充填する。使用時には内
容物を均一に振盪分散して使用する。
Preparation method Component C EGF is blended with component B, and component D ceramide, cerebroside, cholesterol and phospholipid are blended with component A, and components A and B are uniformly dissolved and then component A and component B are mixed. The ingredients are mixed and dispersed by stirring and then filled in a container. At the time of use, the contents should be evenly dispersed by shaking.

【0026】特性 各スキンロ−ションの諸試験を実施した結果を表4に記
載した。比較例1〜6のEGFと角質細胞間脂質を配合
していない、または、どちらか一方のみ配合したスキン
ロ−ションに比較して、本発明の皮膚化粧料は諸試験に
於いて良好な結果が認められた。EGFと角質細胞間脂
質の組み合わせが格段に優れた皮膚機能亢進作用を有す
ることは明らかであった。
Properties The results of various tests of each skin lotion are shown in Table 4. The skin cosmetics of the present invention showed good results in various tests as compared with the skin lotions of Comparative Examples 1 to 6 in which the EGF and interkeratinous lipids were not blended or only one of them was blended. Admitted. It was clear that the combination of EGF and keratinocyte lipid had a significantly superior action to promote skin function.

【0027】[0027]

【表4】 [Table 4]

【0028】実施例6〜10、比較例7〜12 [スキンクリ−ム]実施例1〜5と同様に、表5の組成
にて各々のスキンクリ−ムを調製し、諸試験を実施した
結果を表6に示した。
Examples 6 to 10 and Comparative Examples 7 to 12 [Skin Cream] Similar to Examples 1 to 5, each skin cream was prepared with the composition shown in Table 5 and the results of various tests were conducted. The results are shown in Table 6.

【0029】[0029]

【表5】 [Table 5]

【0030】調製法 C成分のEGFはB成分に、D成分のセラミド、セレブ
ロシド、コレステロ−ル、リン脂質はA成分に配合し
て、A、B成分を各々80℃に加熱溶解した後、混合し
て攪拌しつつ、30℃まで冷却して各スキンクリ−ムを
調製した。
Preparation method Component C EGF is blended with component B, and component D ceramide, cerebroside, cholesterol and phospholipid are blended with component A, and components A and B are dissolved by heating at 80 ° C. and then mixed. While stirring, the mixture was cooled to 30 ° C. to prepare each skin cream.

【0031】特性 表6に示すごとく、本発明の皮膚化粧料である実施例6
〜10のスキンクリ−ムは、比較例6〜12と比較して
諸特性のすべてに亘って優れていることは明らかであ
る。
Properties As shown in Table 6, Example 6 which is the skin cosmetic of the present invention
It is clear that the skin creams of Nos. 10 to 10 are excellent in all of the characteristics as compared with Comparative Examples 6 to 12.

【0032】[0032]

【表6】 [Table 6]

【0033】[0033]

【発明の効果】以上記載のごとく、本発明は、皮膚老化
防止効果(荒れ肌改善効果、角質改善効果、角質層のタ
−ンオ−バ−を速くする効果、美肌効果等)の優れた皮
膚化粧料を提供することができる。
Industrial Applicability As described above, the present invention is a skin makeup excellent in the effect of preventing skin aging (effect of improving rough skin, effect of improving keratin, effect of accelerating turnover of horny layer, beautiful skin effect, etc.). Fees can be provided.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 上皮成長因子と、セラミド、セレブロシ
ド、コレステロ−ルおよびリン脂質より選択された少な
くとも1つとを配合することを特徴とする皮膚化粧料。
1. A skin cosmetic comprising an epidermal growth factor and at least one selected from ceramide, cerebroside, cholesterol and phospholipid.
JP20045093A 1993-07-19 1993-07-19 Skin cosmetic Pending JPH0733637A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20045093A JPH0733637A (en) 1993-07-19 1993-07-19 Skin cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20045093A JPH0733637A (en) 1993-07-19 1993-07-19 Skin cosmetic

Publications (1)

Publication Number Publication Date
JPH0733637A true JPH0733637A (en) 1995-02-03

Family

ID=16424510

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20045093A Pending JPH0733637A (en) 1993-07-19 1993-07-19 Skin cosmetic

Country Status (1)

Country Link
JP (1) JPH0733637A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001181176A (en) * 1999-12-23 2001-07-03 Koreana Cosmetics Co Ltd Cosmetic composition for protecting skin comprising retinol and epidermal growth factor
EP1206932A1 (en) * 1999-08-24 2002-05-22 Kao Corporation Cosmetics
KR100371491B1 (en) * 1999-07-27 2003-02-07 주식회사 두산 Cream Composition For Skin Care
JP2007522259A (en) * 2004-10-20 2007-08-09 ドゥサン コーポレーション A composition containing phosphatidylserine for skin maintenance / improvement or skin barrier function enhancement
JP2009132678A (en) * 2004-05-26 2009-06-18 L'oreal Sa Use of lif in cosmetics and dermatology
JP2010208950A (en) * 2009-03-06 2010-09-24 Nippon Zettoc Co Ltd Cosmetic and manufacturing method of the same
JP2010208949A (en) * 2009-03-06 2010-09-24 Nippon Zettoc Co Ltd Cosmetic and manufacturing method of the same
US7817954B2 (en) 2007-10-09 2010-10-19 Ricoh Company Limited Cleaning unit, image carrier unit including same, and image forming apparatus including same
JP2011195550A (en) * 2010-03-24 2011-10-06 Unitika Ltd Epidermal cell growth promoter and skin external preparation
US8041281B2 (en) 2007-02-14 2011-10-18 Ricoh Company Limited Cleaning device, image forming apparatus, and process cartridge
US8699908B2 (en) 2010-10-22 2014-04-15 Ricoh Company, Ltd. Cleaning device and image forming apparatus including same

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KR100371491B1 (en) * 1999-07-27 2003-02-07 주식회사 두산 Cream Composition For Skin Care
EP1206932A1 (en) * 1999-08-24 2002-05-22 Kao Corporation Cosmetics
EP1206932A4 (en) * 1999-08-24 2005-09-14 Kao Corp Cosmetics
JP2001181176A (en) * 1999-12-23 2001-07-03 Koreana Cosmetics Co Ltd Cosmetic composition for protecting skin comprising retinol and epidermal growth factor
JP2009132678A (en) * 2004-05-26 2009-06-18 L'oreal Sa Use of lif in cosmetics and dermatology
JP2007522259A (en) * 2004-10-20 2007-08-09 ドゥサン コーポレーション A composition containing phosphatidylserine for skin maintenance / improvement or skin barrier function enhancement
US8041281B2 (en) 2007-02-14 2011-10-18 Ricoh Company Limited Cleaning device, image forming apparatus, and process cartridge
US7817954B2 (en) 2007-10-09 2010-10-19 Ricoh Company Limited Cleaning unit, image carrier unit including same, and image forming apparatus including same
JP2010208950A (en) * 2009-03-06 2010-09-24 Nippon Zettoc Co Ltd Cosmetic and manufacturing method of the same
JP2010208949A (en) * 2009-03-06 2010-09-24 Nippon Zettoc Co Ltd Cosmetic and manufacturing method of the same
JP2011195550A (en) * 2010-03-24 2011-10-06 Unitika Ltd Epidermal cell growth promoter and skin external preparation
US8699908B2 (en) 2010-10-22 2014-04-15 Ricoh Company, Ltd. Cleaning device and image forming apparatus including same

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