JPH05294837A - Sebum-secretion promoting agent - Google Patents
Sebum-secretion promoting agentInfo
- Publication number
- JPH05294837A JPH05294837A JP9775292A JP9775292A JPH05294837A JP H05294837 A JPH05294837 A JP H05294837A JP 9775292 A JP9775292 A JP 9775292A JP 9775292 A JP9775292 A JP 9775292A JP H05294837 A JPH05294837 A JP H05294837A
- Authority
- JP
- Japan
- Prior art keywords
- sebum
- agent
- skin
- maltooligosaccharide
- secretion
- 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
Links
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は内服用皮脂分泌促進剤に
関し、更に詳細には、皮脂分泌機能の低下に伴う皮膚症
状、疾患を根本的、全身的に改善することができ、しか
も安全性の高い内服用皮脂分泌促進剤に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sebum secretagogue for internal use, and more specifically, it can fundamentally and systemically improve skin symptoms and diseases associated with a decrease in sebum secretory function and is safe. Highly effective oral sebum secretagogue.
【0002】[0002]
【従来の技術】健康で美しい肌を保つということは、特
に女性にとっては非常に関心の高い問題である。しか
し、肌の状態は湿度、紫外線、化粧品、加齢、疾病、ス
トレス、食習慣等の因子に常に影響され、その結果とし
て肌の諸機能の減退、あるいは過剰な亢進が起こり、様
々な肌のトラブルが発生する。皮脂分泌機能が過剰に亢
進すると尋常性ざ瘡(ニキビ)等の発症の原因となるこ
とがよく知られており、これに対しては皮脂分泌抑制剤
の開発がさかんに行われている。2. Description of the Related Art Maintaining healthy and beautiful skin is a very interesting problem, especially for women. However, the condition of the skin is constantly affected by factors such as humidity, ultraviolet rays, cosmetics, aging, diseases, stress, and eating habits, and as a result, various functions of the skin are diminished or excessively increased, and various skin conditions are caused. Trouble occurs. It is well known that an excessive increase in the sebum secretion function causes the development of acne vulgaris (acne) and the like, and a sebum secretion inhibitor has been vigorously developed for this.
【0003】一方、皮脂分泌機能が低下すると、皮脂膜
の形成が不十分なものとなり、皮膚に保持されている水
分の蒸散量が増加するため、肌あれ、かさつき、ひび、
あかぎれ等の乾燥に起因する疾患の原因となることが知
られている。特に空気の乾燥している冬期には、普通
肌、脂性肌の人でも皮脂分泌機能の低下によってこのよ
うな症状を呈すことが多い。また、皮脂分泌機能は加齢
に伴って低下するため、中年期以降は肌あれ、かさつき
等の症状が顕著にみられるようになり、更に肌の潤い、
つや、なめらかさ、はり、柔軟さ等の特性までも低下す
る。老人性乾皮症は更に重篤な皮膚症状の例であり、強
い掻痒、皮膚の落屑、亀裂を伴うこともある。On the other hand, when the function of secreting sebum decreases, the formation of the sebum film becomes insufficient and the amount of water retained on the skin evaporates, so that the skin becomes rough, rough, cracked,
It is known to cause diseases such as cracks caused by dryness. Particularly in the winter when the air is dry, even people with normal skin or oily skin often exhibit such symptoms due to a decrease in sebum secretion function. In addition, since the sebum secretory function decreases with aging, symptoms such as skin roughness and bulkiness become prominent after the middle age period, and further moisturization of the skin,
Properties such as gloss, smoothness, beam, and flexibility are also reduced. Senile xerosis is an example of a more severe skin condition, which may be accompanied by intense pruritus, skin scaling, and fissures.
【0004】従来、このような皮膚症状を改善する対策
としては、皮脂類似成分、グリセリン、プロピレングリ
コール等の保湿剤、あるいは種々の皮脂分泌促進剤等の
外用剤を皮膚に塗布するという方法がとられてきた。こ
れまでに皮脂分泌促進剤として報告されている物質とし
ては、γ−オリザノール(小林敏夫、早川律子:皮膚、
21、123、1979)、パンテチン脂肪酸エステル
類(特開昭54−160315号)、分岐脂肪酸コレス
テリルエステル類(特開昭60−16927号)、活性
化ビタミンD3 (特開昭62−263125号)、プロ
ポリス抽出物(特開平1−290614号)等が挙げら
れる。[0004] Conventionally, as a measure to improve such skin symptoms, a method of applying a skin moisturizer such as sebum-like components, glycerin, propylene glycol or the like, or an external preparation such as various sebum secretagogues to the skin has been proposed. Has been. Examples of substances that have been reported as sebum secretagogues include γ-oryzanol (Toshio Kobayashi, Ritsuko Hayakawa: skin,
21, 123,1979), pantethine fatty acid esters (JP 54-160315), branched fatty cholesteryl esters (JP-60-16927), activated vitamin D 3 (JP 62-263125) , Propolis extract (JP-A-1-290614), and the like.
【0005】[0005]
【発明が解決しようとする課題】しかしながら、皮脂類
似成分や保湿剤を塗布しても、その改善効果は一時的、
局所的なものであり、根本的な解決手段とはならなかっ
た。また、これまでに知られている皮脂分泌促進剤等か
ら得られる効果も充分満足のいくものではなかった。更
に、これら外用剤はクリーム、軟膏等として皮膚に塗布
するため、その使用に際しては、ベタベタする、油っぽ
いといった不快な使用感があったり、すぐに水洗除去さ
れてしまうという欠点もあった。However, even if a sebum-like component or a moisturizer is applied, the improving effect is temporary,
It was local and did not represent a fundamental solution. In addition, the effects obtained from the sebum secretagogues known so far have not been sufficiently satisfactory. Furthermore, since these external preparations are applied to the skin as creams, ointments, etc., they have the drawback that they are uncomfortable to be used, such as being sticky or oily, or they are quickly washed off with water.
【0006】従って、皮脂分泌機能の低下に伴う皮膚症
状、疾患を根本的、全身的に改善する皮脂分泌促進剤が
望まれていた。[0006] Therefore, there has been a demand for a sebum secretagogue which fundamentally and systemically improves skin symptoms and diseases associated with a decrease in sebum secretory function.
【0007】かかる実情において、本発明者らは鋭意研
究を行った結果、マルトオリゴ糖から成る皮脂分泌促進
剤を内服すれば、皮脂腺機能を根本的、全身的に、しか
も安全に改善できることを見出し、本発明を完成した。Under the circumstances, the inventors of the present invention have conducted diligent research and as a result, found that the sebaceous gland function can be fundamentally, systemically and safely improved by taking a sebum secretagogue consisting of maltooligosaccharide. The present invention has been completed.
【0008】すなわち、本発明は、マルトオリゴ糖から
成る内服用皮脂分泌促進剤を提供するものである。[0008] That is, the present invention provides a sebum secretagogue for internal use, which comprises maltooligosaccharides.
【0009】本発明で用いられるマルトオリゴ糖は公知
の物質であり、グルコースが2〜10分子、α−1,4
グルコシド結合で直鎖状に重合したオリゴ糖である。グ
ルコースが2分子重合したマルトースは、天然には麦芽
水飴の主成分として存在し、3分子以上重合したマルト
オリゴ糖も水飴中に含まれる。これらのマルトオリゴ糖
のうち、特にグルコースの重合度が3〜5であるもの、
すなわち、マルトトリオース、マルトテトラオース、マ
ルトペンタオースが好ましい。The maltooligosaccharide used in the present invention is a known substance, and glucose has 2 to 10 molecules, α-1,4.
It is an oligosaccharide polymerized linearly by a glucoside bond. Maltose in which two molecules of glucose are polymerized naturally exists as the main component of malt syrup, and malto-oligosaccharide in which three or more molecules are polymerized is also contained in syrup. Among these maltooligosaccharides, those having a degree of polymerization of glucose of 3 to 5,
That is, maltotriose, maltotetraose, and maltopentaose are preferable.
【0010】マルトオリゴ糖の製造法としては、特に制
限されないが、例えば澱粉等から酸、α−アミラーゼ等
で部分加水分解する方法、特定の重合度のマルトオリゴ
糖を特異的に生成する微生物起源のマルトオリゴ糖生成
アミラーゼを利用する方法等により製造することができ
る。これらのマルトオリゴ糖はその用法、用途、剤型、
その他目的に応じて精製すればよいが、内服する場合の
投与量、あるいはその効果等を勘案して、できる限り高
純度のマルトオリゴ糖を用いることが望ましい。The method for producing maltooligosaccharides is not particularly limited, but for example, a method of partially hydrolyzing starch or the like with an acid, α-amylase or the like, a maltooligosaccharide of a microorganism origin that specifically produces maltooligosaccharides having a specific degree of polymerization It can be produced by a method utilizing a sugar-forming amylase. These malto-oligosaccharides have their usages, uses, dosage forms,
Although it may be purified according to other purposes, it is desirable to use as high a purity of maltooligosaccharide as possible in consideration of the dose for oral administration, its effect and the like.
【0011】このようにして得られるマルトオリゴ糖
は、一般には、無色透明の液状又は白色粉末である。マ
ルトオリゴ糖は無臭で味覚に優れ、まろやかな甘味を有
し、また、耐酸性、耐熱性にも優れた糖質である。ま
た、LD50はラットで20g/kg以上と、安全性にも優
れたものである。従って、これをそのまま皮脂分泌促進
剤として用いることができ、さらに製薬上許容すること
のできる添加剤や他の薬剤と組合わせて用いることもで
きる。The maltooligosaccharide thus obtained is generally a colorless and transparent liquid or white powder. Malto-oligosaccharides are odorless, have excellent taste, have a mellow sweetness, and are also sugars excellent in acid resistance and heat resistance. In addition, LD 50 is 20 g / kg or more in rats, which is excellent in safety. Therefore, it can be used as it is as a sebum secretagogue, and can also be used in combination with a pharmaceutically acceptable additive or other drug.
【0012】本発明の皮脂分泌促進剤の剤型は、効果を
得るに適したものであれば特に制限されず、例えば、粉
末、散剤、顆粒剤、錠剤、カプセル剤、液剤等とするこ
とができる。The dosage form of the sebum secretagogue of the present invention is not particularly limited as long as it is suitable for obtaining the effect, and may be, for example, powder, powder, granules, tablets, capsules, liquids and the like. it can.
【0013】本発明の皮脂分泌促進剤の投与量は、年
齢、症状等により異なるが、一般に、マルトオリゴ糖と
して、体重1kg、1日あたり10〜3000mg、特に1
00〜1000mgが好ましく、これを1日1回又は数回
に分けて投与することができる。The dose of the sebum secretagogue of the present invention varies depending on age, symptoms and the like, but generally, as maltooligosaccharide, 1 kg of body weight, 10 to 3000 mg per day, particularly 1
The amount is preferably 0.00 to 1000 mg, and this can be administered once or several times a day.
【0014】本発明の皮脂分泌促進剤は、内服すること
により皮脂腺機能を改善することができ、また食品加工
上の特性にも優れることから、美容食品、健康食品等の
食品、飲料、その他医薬品等として応用することができ
る。The sebum secretagogue of the present invention can improve sebaceous gland function by oral administration and is excellent in food processing characteristics. Therefore, it can be used as foods such as beauty foods and health foods, beverages and other pharmaceuticals. And so on.
【0015】[0015]
【発明の効果】本発明の内服用皮脂分泌促進剤は、皮脂
分泌機能の低下に伴う皮膚症状、疾患を根本的、全身的
に改善することができ、しかも安全性の高いものであ
る。また、内服剤であるため、塗布による不快な使用感
や水洗除去されるという欠点もない。INDUSTRIAL APPLICABILITY The sebum secretagogue for oral administration of the present invention is capable of fundamentally and systemically improving skin symptoms and diseases associated with a decrease in sebum secretory function, and is highly safe. Further, since it is an internal medicine, it does not have an unpleasant feeling due to application or the drawback of being removed by washing with water.
【0016】[0016]
【実施例】次に、実施例を挙げて本発明を更に説明す
る。 実施例1 Wister系雌性ラット(6週齢)にマルトオリゴ糖
を含む粉末飼料を自由摂取させて1ケ月間飼育した。粉
末飼料の組成は表1に示すとおりであり、マルトオリゴ
糖は、マルトトリオースを80%以上含有するマルトト
リオースシロップを用い、コントロールとしてマルトオ
リゴ糖の代わりにグルコースを用いた。マルトオリゴ糖
の投与量は、体重1kg、1日あたり150、450、1
500mgとなるように調整した。投与1ケ月後、ラット
背部を剃毛し、4mlアセトン:ジエチルエーテル(1:
1)液でカップ法により経時的に皮脂を抽出した。抽出
した皮脂は秤量瓶に採取し、乾固後、重量法で皮脂分泌
量を測定した。結果を表2に示す。EXAMPLES Next, the present invention will be further described with reference to examples. Example 1 Female Wister rats (6 weeks old) were allowed to freely ingest a powder feed containing maltooligosaccharides, and were bred for one month. The composition of the powdered feed is as shown in Table 1. As the maltooligosaccharide, maltotriose syrup containing 80% or more of maltotriose was used, and glucose was used instead of maltooligosaccharide as a control. The dose of malto-oligosaccharide is 1kg body weight, 150, 450 per day, 1
It was adjusted to be 500 mg. One month after administration, the back of the rat was shaved and 4 ml of acetone: diethyl ether (1:
1) Sebum was extracted with the liquid by the cup method over time. The extracted sebum was collected in a weighing bottle, dried, and then the amount of sebum secreted was measured by a gravimetric method. The results are shown in Table 2.
【0017】[0017]
【表1】 [Table 1]
【0018】[0018]
【表2】 [Table 2]
【0019】表2の結果から明らかなように、マルトオ
リゴ糖投与群では皮脂分泌量が増加する傾向が認められ
た。なお、各飼料群間には、摂食量、増体量に有意な差
は認められなかった。As is clear from the results shown in Table 2, the sebum secretion tended to increase in the maltooligosaccharide-administered group. No significant difference in food intake or body weight gain was observed between the feed groups.
【0020】実施例2 ゴールデンハムスター(7週齢、雌性)にマルトオリゴ
糖水溶液1mlを毎日1回、3週間経口投与した。マルト
オリゴ糖水溶液の組成は表3に示すとおりであり、マル
トオリゴ糖は、マルトトリオースを80%以上含有する
マルトトリオース粉末を用い、コントロールとしてマル
トオリゴ糖の代わりにグルコースを用いた。マルトオリ
ゴ糖の投与量は、体重1kg、1日あたり100、20
0、400、1000mgとした。投与3週間後、ハムス
ター耳介内側部より6mmφの皮膚片を切り取り、軟骨を
除去した後、14C−酢酸ナトリウムを含むクレブス・リ
ンゲル・リン酸緩衝液に浮遊させ、器官培養を行った。
器官培養は37℃で3時間行った。培養後、皮膚片をク
レブス・リンゲル・リン酸緩衝液で洗浄し、10%水酸
化カリウムエタノール溶液で処理した後、2mlヘキサン
にて脂質を抽出し、脂質中の放射活性を測定した。結果
を図1に示す。Example 2 A golden hamster (7 weeks old, female) was orally administered with 1 ml of an aqueous maltooligosaccharide solution once a day for 3 weeks. The composition of the malto-oligosaccharide aqueous solution is as shown in Table 3, and the malto-oligosaccharide used was maltotriose powder containing 80% or more of maltotriose, and glucose was used instead of malto-oligosaccharide as a control. Malto-oligosaccharide dosage is 1kg body weight, 100,20 per day
It was set to 0, 400, and 1000 mg. Three weeks after the administration, a 6 mmφ skin piece was cut out from the inner part of the pinna of the hamster to remove cartilage, and then suspended in Krebs-Ringer-phosphate buffer containing 14 C-sodium acetate, and organ culture was performed.
Organ culture was carried out at 37 ° C for 3 hours. After culturing, the skin pieces were washed with Krebs-Ringer-phosphate buffer solution, treated with 10% potassium hydroxide ethanol solution, and then extracted with 2 ml of hexane to measure the radioactivity in the lipid. The results are shown in Figure 1.
【0021】[0021]
【表3】 [Table 3]
【0022】図1の結果から明らかなように、マルトオ
リゴ糖投与群は、コントロール群に比して、14C−酢酸
ナトリウムの取り込み量で示される脂質合成能が高まる
傾向にあることが示された。なお、各飼料群間には、摂
食量、増体量に有意な差は認められなかった。As is clear from the results shown in FIG. 1, the maltooligosaccharide-administered group tended to have a higher lipid-synthesizing ability, which is indicated by the amount of 14 C-sodium acetate incorporated, as compared with the control group. . No significant difference in food intake or body weight gain was observed between the feed groups.
【0023】実施例3 Wister系雌性ラット(6週齢)に各種オリゴ糖を
含む粉末飼料を自由摂取させて1ケ月間飼育した。粉末
飼料の組成は表4に示すとおりであり、オリゴ糖には、
マルトオリゴ糖の他にフラクトオリゴ糖、イソマルトオ
リゴ糖、パラチノースオリゴ糖、キシロオリゴ糖を用
い、コントロールとしてオリゴ糖の代わりにグルコース
を用いた。各オリゴ糖の投与量は、それぞれ体重1kg、
1日あたり1500mgとなるように調整した。投与1ケ
月後、実施例1と同様の方法で皮脂分泌量を測定した。
コントロール群の皮脂分泌量を100としたときの各オ
リゴ糖投与群の皮脂分泌量を表5に示す。Example 3 Female Wister rats (6 weeks old) were allowed to freely ingest a powdered feed containing various oligosaccharides and bred for one month. The composition of the powdered feed is shown in Table 4, and the oligosaccharides include
In addition to maltooligosaccharides, fructooligosaccharides, isomaltooligosaccharides, palatinose oligosaccharides, and xylooligosaccharides were used. As a control, glucose was used instead of oligosaccharides. The dosage of each oligosaccharide is 1 kg body weight,
It was adjusted to 1500 mg per day. One month after the administration, the amount of sebum secretion was measured by the same method as in Example 1.
Table 5 shows the sebum secretion amount of each oligosaccharide administration group when the sebum secretion amount of the control group was 100.
【0024】[0024]
【表4】 [Table 4]
【0025】[0025]
【表5】 [Table 5]
【0026】表5の結果から明らかなように、マルトオ
リゴ糖以外のオリゴ糖には皮脂分泌促進効果は認められ
なかった。なお、各飼料群間には、摂食量、増体量に有
意な差は認められなかった。As is clear from the results of Table 5, no oligosaccharides other than maltooligosaccharides were found to have a sebum secretion promoting effect. No significant difference in food intake or body weight gain was observed between the feed groups.
【図1】実施例2における14C−酢酸ナトリウム取り込
み量を示す図面である。FIG. 1 is a drawing showing the amount of 14 C-sodium acetate uptake in Example 2.
Claims (2)
促進剤。1. A sebum secretagogue for internal use, which comprises maltooligosaccharide.
が3〜5のマルトオリゴ糖である請求項1記載の皮脂分
泌促進剤。2. The sebum secretagogue according to claim 1, wherein the maltooligosaccharide is a maltooligosaccharide having a glucose polymerization degree of 3 to 5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9775292A JPH05294837A (en) | 1992-04-17 | 1992-04-17 | Sebum-secretion promoting agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9775292A JPH05294837A (en) | 1992-04-17 | 1992-04-17 | Sebum-secretion promoting agent |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH05294837A true JPH05294837A (en) | 1993-11-09 |
Family
ID=14200618
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9775292A Pending JPH05294837A (en) | 1992-04-17 | 1992-04-17 | Sebum-secretion promoting agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH05294837A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6475979B2 (en) | 1999-10-20 | 2002-11-05 | Grain Processing Corporation | Reduced malto-oligosaccharide cleansing compositions |
US6610672B2 (en) | 1999-10-20 | 2003-08-26 | Grain Processing Corporation | Compositions including reduced malto-oligosaccharide preserving agents, and methods for preserving a material |
US6720418B2 (en) | 1999-08-20 | 2004-04-13 | Grain Processing Corporation | Derivatized reduced malto-oligosaccharides |
US6919446B1 (en) | 1998-01-20 | 2005-07-19 | Grain Processing Corp. | Reduced malto-oligosaccharides |
WO2008047709A1 (en) * | 2006-10-16 | 2008-04-24 | Lion Corporation | Nk1 receptor antagonist composition |
US7405293B1 (en) | 1998-01-20 | 2008-07-29 | Grain Processing Corporation | Reduced malto-oligosaccharides |
JP2013032366A (en) * | 2007-05-25 | 2013-02-14 | Hayashibara Co Ltd | Sebum amount decrease inhibitor containing alpha-glycosyl hesperidin for use in oral administration/ingestion |
-
1992
- 1992-04-17 JP JP9775292A patent/JPH05294837A/en active Pending
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6919446B1 (en) | 1998-01-20 | 2005-07-19 | Grain Processing Corp. | Reduced malto-oligosaccharides |
US7405293B1 (en) | 1998-01-20 | 2008-07-29 | Grain Processing Corporation | Reduced malto-oligosaccharides |
US7595393B2 (en) | 1998-01-20 | 2009-09-29 | Grain Processing Corporation | Reduced malto-oligosaccharides |
US6720418B2 (en) | 1999-08-20 | 2004-04-13 | Grain Processing Corporation | Derivatized reduced malto-oligosaccharides |
US6475979B2 (en) | 1999-10-20 | 2002-11-05 | Grain Processing Corporation | Reduced malto-oligosaccharide cleansing compositions |
US6610672B2 (en) | 1999-10-20 | 2003-08-26 | Grain Processing Corporation | Compositions including reduced malto-oligosaccharide preserving agents, and methods for preserving a material |
WO2008047709A1 (en) * | 2006-10-16 | 2008-04-24 | Lion Corporation | Nk1 receptor antagonist composition |
US8426386B2 (en) | 2006-10-16 | 2013-04-23 | Lion Corporation | NK1 receptor antagonist composition |
JP5204657B2 (en) * | 2006-10-16 | 2013-06-05 | ライオン株式会社 | NK1 receptor antagonist composition |
JP2013032366A (en) * | 2007-05-25 | 2013-02-14 | Hayashibara Co Ltd | Sebum amount decrease inhibitor containing alpha-glycosyl hesperidin for use in oral administration/ingestion |
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