JPH08175965A - Skin cosmetic - Google Patents

Skin cosmetic

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Publication number
JPH08175965A
JPH08175965A JP33783394A JP33783394A JPH08175965A JP H08175965 A JPH08175965 A JP H08175965A JP 33783394 A JP33783394 A JP 33783394A JP 33783394 A JP33783394 A JP 33783394A JP H08175965 A JPH08175965 A JP H08175965A
Authority
JP
Japan
Prior art keywords
skin
acid
effect
cosmetic
test
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
JP33783394A
Other languages
Japanese (ja)
Inventor
Norihiko Seko
典彦 世古
Tatsu Miyamoto
達 宮本
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 JP33783394A priority Critical patent/JPH08175965A/en
Publication of JPH08175965A publication Critical patent/JPH08175965A/en
Pending legal-status Critical Current

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Abstract

PURPOSE: To obtain a skin cosmetic excellent in aged skin-curing effect such as chapped skin-curing effect, corneum-improving effect, stratum corneum turnover-accelerating effect and skin-beautifying effect, formulated with salt(s) of specific organic acid(s) such as malic acid and nicotinic alcohol. CONSTITUTION: This cosmetic stands formulated with pref. 0.001-5.0wt.% of slat(s) of nicotinic alcohol and at least one kind of organic acid selected from malic acid, citric acid, succinic acid, lactic acid, glycolic acid, fumaric acid and maleic acid. This cosmetic is applied in the form of lotion, milky lotion, cream, park, etc.

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、角質層のターンオーバー
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。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a skin cosmetic having excellent aged skin improving effect (rough skin improving effect, keratin improving effect, horny layer turnover accelerating effect, beautiful skin effect, etc.).

【0002】[0002]

【従来の技術および発明が解決しようとする課題】老化
皮膚とは、表面では乾燥して滑らかさがなく、荒れ肌や
角質細胞の剥離現象も認められる。また、表皮の細胞数
は減少し、細胞代謝の低下により表皮全体の代謝速度や
角質層のターンオーバー速度が遅くなることが知られて
いる。一方、真皮の結合組織では、コラーゲン線維が細
くなり、線維の間隙が拡大し、ヒアルロン酸等の基質成
分も減少することから、しわやたるみの原因となってい
る。更に、毛細血管密度の減少や、末梢血流の循環不良
が原因となり、栄養補給や老廃物の除去が円滑に出来な
くなっている。以上のような観点から、老化皮膚におけ
る血行不良を改善することにより、老化皮膚の諸症状が
改善されることから、種々の皮膚血行促進物質や細胞賦
活成分が研究されている。
2. Description of the Related Art Aged skin has a dry and non-smooth surface, and rough skin and exfoliation of keratinocytes are also recognized. In addition, it is known that the number of cells in the epidermis is decreased and the metabolic rate of the entire epidermis and the turnover rate of the stratum corneum are slowed due to the decrease in cell metabolism. On the other hand, in the connective tissue of the dermis, collagen fibers become thin, the interstices of the fibers widen, and matrix components such as hyaluronic acid also decrease, which causes wrinkles and sagging. Furthermore, nutritional supplementation and removal of waste products cannot be performed smoothly due to a decrease in capillary density and poor circulation of peripheral blood flow. From the above viewpoints, various symptoms of aging skin are improved by improving poor circulation in aging skin, and thus various skin blood circulation promoting substances and cell activating components have been studied.

【0003】ビタミンE等を配合した皮膚の治療および
保護薬が、皮膚の湿疹、炎症、しわ等に有効であると提
案されている(特開昭61−40210号公報)。しか
し、実用上に於いてビタミンE単独あるいはビタミンE
と他の成分を配合した外用薬を皮膚に適用しても、組織
機能を修復または改善し、皮膚が元来保有する機能を回
復して皮膚の老化防止効果に著効を示す程度に効果を発
揮するまでには至らなかった。
It has been proposed that a therapeutic and protective drug for the skin containing vitamin E or the like is effective against skin eczema, inflammation, wrinkles and the like (Japanese Patent Laid-Open No. 61-40210). However, in practice, vitamin E alone or vitamin E
Even if an external medicine containing this and other ingredients is applied to the skin, it is effective enough to repair or improve the tissue function, restore the function originally possessed by the skin, and exert a remarkable effect on the antiaging effect of the skin. It didn't come out to the point.

【0004】本発明の目的は、皮膚老化防止効果(荒れ
肌改善効果、角質改善効呆、角質層のターンオーバーを
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。
An object of the present invention is to provide a skin cosmetic having an excellent 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.).

【0005】[0005]

【課題を解決するための手段】本発明者らは、上記の事
情に鑑み鋭意研究した結果、リンゴ酸、クエン酸、コハ
ク酸、乳酸、グリコール酸、フマル酸、マレイン酸から
なる群から選ばれる一種以上の有機酸とニコチニックア
ルコールとの塩を配合した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、角質層のターンオ
ーバーを速くする効果、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。
Means for Solving the Problems As a result of intensive studies in view of the above circumstances, the present inventors have selected from the group consisting of malic acid, citric acid, succinic acid, lactic acid, glycolic acid, fumaric acid, and maleic acid. Skin cosmetics containing one or more salts of organic acid and nicotinic alcohol are excellent in improving aging skin (effects of improving rough skin, improving keratin, accelerating turnover of stratum corneum, and skin beautifulness). After confirmation, the present invention was completed.

【0006】本発明のニコチニックアルコールと特定の
有機酸との塩を配合してなる皮膚化粧料は、皮膚に対す
る浸透性が高く、表皮細胞の増殖および分化の促進、さ
らに、末梢血管を拡張して皮膚機能をこう進し、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
果が認められる。
The skin cosmetic composition of the present invention containing a salt of nicotinic alcohol and a specific organic acid has high permeability to the skin, promotes proliferation and differentiation of epidermal cells, and further expands peripheral blood vessels. When it is applied to aged skin by enhancing or improving the skin function and restoring or improving the function originally possessed by the skin to keep the skin in a healthy state, a remarkable effect is observed.

【0007】ニコチニックアルコール(3−ピリジンメ
タノール)は、公知の物質であり、末梢血流促進作用を
有する薬剤として肝臓疾患や脳機能改善剤として使用さ
れている。また、本発明に用いる有機酸の種類として、
リンゴ酸、クエン酸、コハク酸、乳酸、グリコール酸、
フマル酸、マレイン酸が挙げられるが、特にリンゴ酸、
クエン酸、コハク酸、乳酸、グリコール酸が好ましい。
Nicotinic alcohol (3-pyridinemethanol) is a known substance and is used as a liver disease and brain function improving agent as a drug having a peripheral blood flow promoting action. Further, as the type of organic acid used in the present invention,
Malic acid, citric acid, succinic acid, lactic acid, glycolic acid,
Examples include fumaric acid and maleic acid, but especially malic acid,
Citric acid, succinic acid, lactic acid and glycolic acid are preferred.

【0008】ニコチニックアルコールの上記有機酸塩
は、以下の方法により容易に調製が可能である。ニコチ
ニックアルコールを1〜30%に、また有機酸を1〜1
0%にそれぞれエチルアルコールに溶解させる。次に、
等モル量になるように両液を室温で混合し、1時間程度
放置する。その後に、生成した結晶をろ過し、目的のニ
コチニックアルコールの有機酸塩を得ることが出来る。
また、結晶が生成しない場合には、溶媒のエタノールを
減圧留去し、液状のニコチニックアルコールの有機酸塩
を得ることが出来る。
The above organic acid salt of nicotinic alcohol can be easily prepared by the following method. Nicotinic alcohol to 1-30%, organic acids 1-1
Dissolve in 0% each in ethyl alcohol. next,
Both solutions are mixed at room temperature so as to be equimolar amounts and left for about 1 hour. After that, the generated crystals can be filtered to obtain the desired organic acid salt of nicotinic alcohol.
When crystals do not form, the solvent ethanol is distilled off under reduced pressure to obtain a liquid organic acid salt of nicotinic alcohol.

【0009】前記ニコチニックアルコールの有機酸塩の
配合量は、皮膚化粧料の総量を基準として0.001〜
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な
い。
The amount of organic acid salt of nicotinic alcohol is 0.001 to 0.001 based on the total amount of skin cosmetics.
5.0% by weight is preferred. If the compounded 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, the effect commensurate with the increase cannot be obtained.

【0010】本発明の皮膚化粧料は、例えばローション
類、乳液類、クリーム類、パック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, for example, lotions, emulsions, creams, packs and the like. In addition to the above, a colorant, a fragrance, an antiseptic, a surfactant, a pigment, an antioxidant and the like can be appropriately added to the skin cosmetic of the present invention within the range where the object of the present invention is achieved.

【0011】[0011]

【実施例】以下、実施例及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.

【0012】まず、荒れ肌効果試験、角質改善効果試
験、角質層のターンオーバー測定試験、官能テスト(美
肌効果試験)の試験方法について記述する。
First, test methods for rough skin effect test, keratin improvement effect test, horny layer turnover measurement test, and sensory test (skin beauty effect test) will be described.

【0013】〔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4週間連続塗布
効果を調べた。被験者の左側下脚外側試験部位に1日1
回約0.5gの試料を塗布し、試験開始前および終了後
の皮膚の状態を下表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 improving effect test] The effect of continuous application for 4 weeks was investigated for 10 middle-aged and elderly subjects having rough skin on the lower leg. 1 day per day on the left lower leg outer test site of the subject
About 0.5 g of the sample was applied once, and the condition of the skin before and after the start of the test was evaluated according to the criteria shown in the table below. The lower right leg was not coated with the sample and served as a control.

【0014】[0014]

【表1】 [Table 1]

【0015】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.

【0016】〔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チープ(ニチバンメンデイング
テープ)を接着し、これを剥離したテープに付着した角
質細胞の状態を走査型電子顕微鏡によって詳細に調ベ、
下表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。
[Keratin improvement (increased keratinocyte anti-peeling effect) effect test] Scotch cheap (Nichiban Mending Tape) was adhered to the skin of the test area before and after the start of the rough skin improvement effect test described above, and this was peeled off. The state of the keratinocytes attached to the tape is examined in detail using a scanning electron microscope.
The anti-exfoliation property of skin keratinocytes was analyzed according to the criteria in the table below, and the keratin improving effect was obtained.

【0017】[0017]

【表2】 [Table 2]

【0018】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.

【0019】〔角質層の夕一ンオーバー測定試験〕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2
4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回暗所で紫外線ランプ
を用いて、ダンシルクロライドの蛍光を調ベ、その蛍光
が消滅するまでの日数を皮膚角質層のターンオーバーと
した。
[Countermeasurement test of stratum corneum] 5 wt% of dansyl chloride, a fluorescent dye, in white petrolatum
Make a mixed ointment and apply 2 to the skin of the forearm of 10 subjects.
A patch is applied for 4 hours, and dansyl chloride is permeated and bonded to the stratum corneum. After that, about 0.2 g of the test sample was applied to the same site twice a day (morning and evening), and once a day, the fluorescence of dansyl chloride was adjusted using an ultraviolet lamp in a dark place until the fluorescence disappeared. The number of days was defined as the turnover of the stratum corneum of the skin.

【0020】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ーンオーバーは13〜
16日であるか、老化した皮膚においては18日前後に
伸びる。それに対して老化防止効果が現れると13日前
後にまで短縮される。
The measurement results are shown by the average value of the number of days of each subject. Normal turnover of stratum corneum is 13 ~
16 days or around 18 days in aged skin. On the other hand, when the anti-aging effect appears, it is shortened to around 13 days.

【0021】〔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l日2回(朝・夕)連続4週問塗布して
4週間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)] Rough skin,
Female subject (35-55 years old) who complains of fine wrinkles, dry skin, etc.
The sample was applied to 10 people twice a day (morning and evening) for 4 consecutive weeks, and the effect after 4 weeks was evaluated. The test results were expressed by the number of people who answered that the skin was moistened, the skin became smooth, and the skin became taut for each item of skin wettability, smoothness, and elasticity.

【0022】実施例1〜9、比較例1〔スキンローショ
ン〕 表3の組成のごとくスキンローションに表4に記載通り
ニコチニックアルコールの有機酸塩を配合して下記の調
製方法によって各々のスキンローションを調製した。
Examples 1 to 9 and Comparative Example 1 [Skin lotion] The skin lotion having the composition shown in Table 3 was mixed with the organic acid salt of nicotinic alcohol as shown in Table 4, and each skin lotion was prepared by the following preparation method. Was prepared.

【0023】[0023]

【表3】 [Table 3]

【0024】[調製法]C成分のニコチニックアルコー
ルの有機酸塩はB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成分を混合撹伴分散し、次いで
容器に充填する。使用時には内容物を均一に振とう分散
して使用する。
[Preparation Method] The organic acid salt of nicotinic alcohol as the component C is blended with the component B to uniformly dissolve the components A and B, and then the components A and B are mixed and dispersed by stirring, and then the container. To fill. At the time of use, the contents are shaken and dispersed evenly before use.

【0025】前記諸試験を実施した結果を表4に記載し
た。
The results of carrying out the various tests are shown in Table 4.

【0026】[0026]

【表4】 [Table 4]

【0027】実施例1〜9のニコチニックアルコールの
有機酸塩を配合したスキンローションは、比較例1と比
較して、諸試験に於いて良好な結果が認められた。
The skin lotions containing the organic acid salt of nicotinic alcohol of Examples 1 to 9 were found to have good results in various tests as compared with Comparative Example 1.

【0028】実施例10〜18、比較例2[スキンクリ
ーム] 表5の組成にて表6に記載の通り各種ニコチニックアル
コールの有機酸塩を配合して各々のスキンクリームを下
記の調製方法によって調製した。
Examples 10 to 18 and Comparative Example 2 [Skin Cream] Each skin cream was prepared by blending organic acid salts of various nicotinic alcohols as shown in Table 6 with the composition shown in Table 5 by the following preparation method. Prepared.

【0029】[0029]

【表5】 [Table 5]

【0030】[調製法]C成分のニコチニックアルコー
ルの有機酸塩はB成分に配合して、A,B成分を各々8
0℃に加熱溶解した後、混合して撹拌しつつ、30℃ま
で冷却して各スキンクリームを調製した。
[Preparation Method] The organic acid salt of nicotinic alcohol as the component C is blended with the component B, and each of the components A and B is 8
Each skin cream was prepared by heating and dissolving at 0 ° C., then mixing and stirring, and cooling to 30 ° C.

【0031】諸試験を実施した結果を表6に示した。The results of various tests are shown in Table 6.

【0032】[0032]

【表6】 [Table 6]

【0033】表6に示すごとく、本発明の皮膚化粧料で
ある実施例9〜18のスキンクリームは、比較例2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
であった。
As shown in Table 6, it was clear that the skin creams of Examples 9 to 18, which were the skin cosmetics of the present invention, were superior to Comparative Example 2 in all properties. .

【0034】[0034]

【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
ーンオーバーを速くする効果、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 provides 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 the stratum corneum, effect of beautiful skin, etc.). be able to.

【手続補正書】[Procedure amendment]

【提出日】平成7年5月17日[Submission date] May 17, 1995

【手続補正1】[Procedure Amendment 1]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0023[Name of item to be corrected] 0023

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0023】[0023]

【表3】 [Table 3]

【手続補正2】[Procedure Amendment 2]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0029[Name of item to be corrected] 0029

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0029】[0029]

【表5】 [Table 5]

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 リンゴ酸、クエン酸、コハク酸、乳酸、
グリコール酸、フマル酸、マレイン酸からなる群から選
ばれる一種以上の有機酸とニコチニックアルコールとの
塩を配合することを特徴とする皮膚化粧料。
1. Malic acid, citric acid, succinic acid, lactic acid,
A skin cosmetic, comprising a salt of nicotinic alcohol and one or more organic acids selected from the group consisting of glycolic acid, fumaric acid and maleic acid.
JP33783394A 1994-12-26 1994-12-26 Skin cosmetic Pending JPH08175965A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP33783394A JPH08175965A (en) 1994-12-26 1994-12-26 Skin cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP33783394A JPH08175965A (en) 1994-12-26 1994-12-26 Skin cosmetic

Publications (1)

Publication Number Publication Date
JPH08175965A true JPH08175965A (en) 1996-07-09

Family

ID=18312404

Family Applications (1)

Application Number Title Priority Date Filing Date
JP33783394A Pending JPH08175965A (en) 1994-12-26 1994-12-26 Skin cosmetic

Country Status (1)

Country Link
JP (1) JPH08175965A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20010047160A (en) * 1999-11-18 2001-06-15 구명수 New Maleic Acid Derivatives and Their Manufacturing Processes

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20010047160A (en) * 1999-11-18 2001-06-15 구명수 New Maleic Acid Derivatives and Their Manufacturing Processes

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