JPH0881348A - External preparation for skin - Google Patents

External preparation for skin

Info

Publication number
JPH0881348A
JPH0881348A JP21996694A JP21996694A JPH0881348A JP H0881348 A JPH0881348 A JP H0881348A JP 21996694 A JP21996694 A JP 21996694A JP 21996694 A JP21996694 A JP 21996694A JP H0881348 A JPH0881348 A JP H0881348A
Authority
JP
Japan
Prior art keywords
skin
trimethylglycine
external preparation
weight
antiseptic
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
JP21996694A
Other languages
Japanese (ja)
Other versions
JP3577113B2 (en
Inventor
Masashi Takasugi
正史 高杉
Yoshiyuki Matsumoto
能幸 松本
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.)
Kobayashi Pharmaceutical Co Ltd
Original Assignee
Kobayashi Pharmaceutical Co 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 Kobayashi Pharmaceutical Co Ltd filed Critical Kobayashi Pharmaceutical Co Ltd
Priority to JP21996694A priority Critical patent/JP3577113B2/en
Publication of JPH0881348A publication Critical patent/JPH0881348A/en
Application granted granted Critical
Publication of JP3577113B2 publication Critical patent/JP3577113B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE: To obtain an external preparation for skin having both excellent moisture retention power and antiseptic power and low irritation to skin and good feeling in use. CONSTITUTION: This external preparation for skin contains >=20wt.% of trimethylglycine. Trimethylglycine in an amount of <=5wt.% can be replaced with a polyhydric alcohol in an amount of <=5wt.%.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は皮膚外用剤に関し、特に
優れた保湿機能と防腐力を有する皮膚外用剤に関する。
FIELD OF THE INVENTION The present invention relates to a skin external preparation, and more particularly to a skin external preparation having an excellent moisturizing function and antiseptic property.

【0002】[0002]

【従来の技術および発明が解決しようとする課題】皮膚
外用剤は、その内容物が皮膚の分泌物(皮脂膜)の作用
を補う役割をもっているところから、微生物の栄養源に
なりやすく、増殖の場となることがある。
2. Description of the Related Art An external preparation for skin is liable to be a nutrient source for microorganisms because it has a role of supplementing the action of skin secretions (sebum membranes), and thus the external preparation for growth is It may be a place.

【0003】微生物に汚染された皮膚外用剤は変臭、変
質、カビの発生等品質の低下をきたすので、これを防止
する措置を講ずる必要がある。そのため、製造工程を衛
生的に管理することはいうまでもないが、ほとんどの皮
膚外用剤には防腐、殺菌の目的で防腐・殺菌剤が配合さ
れている。
The external preparation for skin contaminated with microorganisms causes deterioration in quality such as odor, deterioration and generation of mold, and it is necessary to take measures to prevent this. Therefore, it goes without saying that the manufacturing process is controlled hygienically, but most of the external preparations for the skin contain antiseptic / bactericidal agents for the purpose of antiseptic and sterilization.

【0004】この点に関して、保湿を目的の1つとした
皮膚外用剤(クリーム、乳液、ローション、ジェル等)
も製剤自身が細菌によって汚染されないようにするた
め、フェノキシエタノール、パラオキシ安息香酸エステ
ル、感光素系・カチオン系・フェノール系等の防腐・殺
菌剤が配合されているが、これらの成分は皮膚刺激の一
因となる場合がある。
[0004] In this regard, external preparations for skin (creams, emulsions, lotions, gels, etc.) whose purpose is to retain moisture.
In order to prevent the formulation itself from being contaminated with bacteria, phenoxyethanol, paraoxybenzoate, and photosensitizer / cation / phenol-based antiseptic / bactericidal agents have been added. It may be a cause.

【0005】保湿と補助的防腐剤を兼用する目的で使用
されている成分としては多価アルコール類があるが、プ
ロピレングリコール、1,3−ブチレングリコール、イ
ソプレングリコール等の多価アルコールのみでは通常十
分な保湿力・防腐力が得られず、一方、これらを単独で
防腐効果のある濃度で使用すれば、皮膚刺激性が発揮さ
れる。
Polyhydric alcohols are used as a component for both moisturizing and auxiliary preservative, but polyhydric alcohols such as propylene glycol, 1,3-butylene glycol and isoprene glycol are usually sufficient. Moisturizing and antiseptic properties are not obtained. On the other hand, when they are used alone in a concentration having an antiseptic effect, skin irritation is exhibited.

【0006】また、グリセリンには保湿力があり、防腐
力を有する高濃度においても刺激は少ないが、ベタツキ
等使用感に問題がある。
[0006] Glycerin has a moisturizing effect and has little anti-irritant effect even at a high concentration having antiseptic effect, but it has a problem in stickiness such as stickiness.

【0007】本発明は従来の技術の有するこのような問
題点に鑑みてなされたものであって、その目的は、優れ
た保湿力と防腐力を兼ね備え、皮膚への刺激が少なく、
使用感の良好な皮膚外用剤を提供することにある。
The present invention has been made in view of the above problems of the prior art, and its object is to have both excellent moisturizing power and antiseptic power and less irritation to the skin.
It is intended to provide an external preparation for skin having a good feeling in use.

【0008】[0008]

【課題を解決するための手段】上記目的を達成するため
に本発明の要旨は、トリメチルグリシンを20重量%以
上含有していることを特徴とする皮膚外用剤を第一の発
明とし、上記第一の発明において、5重量%以下のトリ
メチルグリシンの代わりに、5重量%以下の多価アルコ
ールを使用したことを特徴とする皮膚外用剤を第二の発
明とする。
In order to achieve the above object, the gist of the present invention is to provide a skin external preparation characterized by containing 20% by weight or more of trimethylglycine as a first invention. A second invention is a skin external preparation characterized by using 5% by weight or less of polyhydric alcohol in place of 5% by weight or less of trimethylglycine.

【0009】さらに、目的に応じて、抗炎症成分、局所
麻酔成分、血流促進成分、美白成分等を配合することが
できる。
Further, an anti-inflammatory component, a local anesthetic component, a blood flow promoting component, a whitening component and the like can be added depending on the purpose.

【0010】[0010]

【作用】トリメチルグリシンは砂糖大根の他多くの植物
やエビ、イカ等にも含まれている、人体に安全な天然物
質であり、次に示す構造式で表される。
[Function] Trimethylglycine is a natural substance safe to human body, which is contained in many plants such as sugar beet, shrimp, squid, etc., and is represented by the following structural formula.

【0011】[0011]

【化1】 Embedded image

【0012】上式に示すように、トリメチルグリシンは
グリシンのアミノ基がトリメチル化されて分子内塩を形
成している両イオン性の保湿剤であり、他の保湿剤と保
湿効果を比較したものを図1に示す。同図において、1
はトリメチルグリシンを示し、2はグリセリン、3はソ
ルビット、4はピロリドンカルボン酸ナトリウムを示
す。測定条件としては、各保湿剤を50%水溶液の状態
で準備し、温度30±1℃、相対湿度35±3%の雰囲
気下で放置した場合の残存水分量(%)を日毎に測定す
るという方法によった。図に見られるように、トリメチ
ルグリシンの保湿力は極めて優れている。
As shown in the above formula, trimethylglycine is a zwitterionic moisturizer in which the amino group of glycine is trimethylated to form an inner salt, and its moisturizing effect is compared with other moisturizers. Is shown in FIG. In the figure, 1
Indicates trimethylglycine, 2 indicates glycerin, 3 indicates sorbit, 4 indicates sodium pyrrolidonecarboxylate. As a measurement condition, each moisturizer is prepared in a 50% aqueous solution, and the amount of residual water (%) is measured every day when the moisturizer is left in an atmosphere of a temperature of 30 ± 1 ° C and a relative humidity of 35 ± 3%. According to the method. As shown in the figure, the moisturizing power of trimethylglycine is extremely excellent.

【0013】係る保湿力に優れたトリメチルグリシンを
20重量%以上含有する皮膚外用剤は、角質細胞層に速
やかに浸透し、皮膚に『うるおい』と『なめらかさ』を
与えるとともに優れた防腐力を発揮する。また、5重量
%以下のトリメチルグリシンに代えて、5重量%以下の
多価アルコールを使用しても、防腐力が期待できる。
The skin external preparation containing 20% by weight or more of trimethylglycine, which has an excellent moisturizing power, quickly penetrates into the keratinocyte layer to give the skin "moisture" and "smoothness" and an excellent antiseptic effect. Demonstrate. Even if 5% by weight or less of polyhydric alcohol is used instead of 5% by weight or less of trimethylglycine, antiseptic activity can be expected.

【0014】[0014]

【実施例】次に、本発明の実施例を説明する。以下の表
1のように配合した、処方No.〜(15)の各組成のも
のについて抗菌性の試験を行ったので、その結果を表2
に示す。表1の配合は重量%である。なお、抗菌性の試
験方法は以下のとおりとした。
Next, embodiments of the present invention will be described. Prescription No. compounded as shown in Table 1 below. The antibacterial properties of the compositions of (15) to (15) were tested.
Shown in The formulations in Table 1 are% by weight. The antibacterial test method was as follows.

【0015】〔抗菌性の試験方法〕 (1) 保存菌株(大腸菌、黄色ブドウ球菌または緑膿菌)
より、各菌を平板培地に植菌して24時間培養し、得ら
れた各菌を生理食塩水に分散させ、濁度より約108
の菌液に調整した。
[Test method for antibacterial property] (1) Preserved strain (Escherichia coli, Staphylococcus aureus or Pseudomonas aeruginosa)
Thus, each bacterium was inoculated on a plate medium and cultured for 24 hours, and each bacterium thus obtained was dispersed in physiological saline and adjusted to about 10 8 bacterial solution based on the turbidity.

【0016】(2) 菌液の正確な濃度は、希釈菌液を平板
培養し、コロニー数より求めた。その測定結果は、大腸
菌については3×108 個/ml、黄色ブドウ球菌につい
ては6×108 個/ml、緑膿菌については3×108
/mlであった。
(2) The exact concentration of the bacterial solution was determined from the number of colonies obtained by plating the diluted bacterial solution on a plate. The measurement results were 3 × 10 8 cells / ml for E. coli, 6 × 10 8 cells / ml for Staphylococcus aureus, and 3 × 10 8 cells / ml for Pseudomonas aeruginosa.

【0017】(3) 次に、処方No.〜(15)の試験検体
各10mlに、各菌液をそれぞれ0.1ml植菌し(約10
6 個/ml)、37℃で培養した。
(3) Next, the prescription No. 0.1 ml of each bacterial solution was inoculated to each 10 ml of the test sample of (15) (about 10 ml).
6 cells / ml) and cultured at 37 ° C.

【0018】(4) 7日後および14日後に、以上のよう
にして得た各試験溶液より0.1ml(必要があれば希
釈)を平板培養し、コロニー数を測定して菌数の変化を
求めた。
(4) After 7 days and 14 days, 0.1 ml (diluted if necessary) of each test solution obtained as described above was plated, and the number of colonies was measured to check the change in the number of bacteria. I asked.

【0019】[0019]

【表1】 [Table 1]

【0020】[0020]

【表2】 [Table 2]

【0021】表2より以下の点が明らかである。 (a) トリメチルグリシンが15重量%以下である処方N
o.〜のものには、防腐力は見られない。トリメチ
ルグリシンが10重量%である処方No.のものにメ
チルパラベンを少量添加した、処方No.のものには
多少の防腐力はみられるが、十分ではない。さらに、処
方No.のものにポリオキシエチレン硬化ヒマシ油を
添加した、処方No.のものには防腐力はみられな
い。
The following points are clear from Table 2. (a) Formulation N in which trimethylglycine is 15% by weight or less
o. There is no antiseptic effect in ~. Formulation No. in which trimethylglycine is 10% by weight. Prescription No., in which a small amount of methylparaben was added to the above. Some of them have some antiseptic properties, but they are not enough. Further, the prescription No. Formulation No. obtained by adding polyoxyethylene hydrogenated castor oil to No antiseptic effect is found in the thing.

【0022】(b) 処方No.と(10)との比較より、ト
リメチルグリシンは両性物質であるが、弱酸性にしてカ
チオン化することで防腐力は向上しないことが分かる。
(B) Prescription No. From the comparison between (10) and (10), it can be seen that trimethylglycine is an amphoteric substance, but its preservative power is not improved by weakly acidifying and cationizing.

【0023】(c) トリメチルグリシンが20重量%以上
である処方No.、、(13)、(14)、(15)は、明確な
防腐力を示している。
(C) Prescription No. containing 20% by weight or more of trimethylglycine ,, (13), (14), (15) show a clear antiseptic effect.

【0024】(d) 処方No.の20重量%のトリメチ
ルグリシンのうち、5重量%を多価アルコールに置き換
えた処方No.(11)、(12)は、処方No.と同様の優
れた防腐力を示している。
(D) Prescription No. 20% by weight of trimethylglycine, 5% by weight was replaced with a polyhydric alcohol. (11) and (12) are prescription numbers. It has the same excellent antiseptic properties as.

【0025】(e) トリメチルグリシンが20重量%であ
る処方No.のものに多価アルコールを5重量%添加
した処方No.(13)のものは、処方No.以上の防腐
力を示している。このように、多価アルコールを併用す
ることによって防腐力は増強されるが、低刺激性を考慮
すれば、多価アルコールの添加量は5重量%を上限とす
るのが好ましい。
(E) Recipe No. containing 20% by weight of trimethylglycine Formulation No. in which 5% by weight of polyhydric alcohol was added to (13) is the prescription number. It shows the above antiseptic power. As described above, the antiseptic power is enhanced by using the polyhydric alcohol together, but in consideration of the low irritancy, the addition amount of the polyhydric alcohol is preferably 5% by weight or less.

【0026】(f) 処方No.と(14)、あるいは処方N
o.と(15)の比較で明らかなように、ノニオン活性剤
である、ポリオキシエチレン硬化ヒマシ油を添加して
も、トリメチルグリシンを十分な量保有しているので防
腐力は全く低下しないことが分かる。
(F) Prescription No. And (14) or prescription N
o. As is clear from the comparison between (15) and (15), even if polyoxyethylene hydrogenated castor oil, which is a nonionic activator, is added, preservative power does not decrease at all because it has a sufficient amount of trimethylglycine. .

【0027】[0027]

【発明の効果】本発明は上記のとおり構成されているの
で、優れた防腐力と保湿力を兼ね備え、皮膚への刺激が
少なく、使用感が良好である。また、トリメチルグリシ
ンと多価アルコールを併用することにより、防腐力を一
層向上させることができる。
EFFECTS OF THE INVENTION Since the present invention is constituted as described above, it has excellent antiseptic power and moisturizing power, less irritation to the skin, and good usability. Further, by using trimethylglycine and a polyhydric alcohol in combination, the antiseptic effect can be further improved.

【図面の簡単な説明】[Brief description of drawings]

【図1】各種保湿剤の保湿効果を示す図である。FIG. 1 is a diagram showing the moisturizing effect of various moisturizers.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 トリメチルグリシンを20重量%以上含
有していることを特徴とする皮膚外用剤。
1. A skin external preparation containing 20% by weight or more of trimethylglycine.
【請求項2】 5重量%以下のトリメチルグリシンの代
わりに、5重量%以下の多価アルコールを使用したこと
を特徴とする請求項1記載の皮膚外用剤。
2. The external preparation for skin according to claim 1, wherein 5% by weight or less of polyhydric alcohol is used in place of 5% by weight or less of trimethylglycine.
JP21996694A 1994-09-14 1994-09-14 External preparation for skin Expired - Fee Related JP3577113B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21996694A JP3577113B2 (en) 1994-09-14 1994-09-14 External preparation for skin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21996694A JP3577113B2 (en) 1994-09-14 1994-09-14 External preparation for skin

Publications (2)

Publication Number Publication Date
JPH0881348A true JPH0881348A (en) 1996-03-26
JP3577113B2 JP3577113B2 (en) 2004-10-13

Family

ID=16743828

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21996694A Expired - Fee Related JP3577113B2 (en) 1994-09-14 1994-09-14 External preparation for skin

Country Status (1)

Country Link
JP (1) JP3577113B2 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11217211A (en) * 1998-01-30 1999-08-10 Shiseido Co Ltd Sol composition
US6156293A (en) * 1997-01-03 2000-12-05 Finnfedds Finland Ltd. Moistening preparation
US6165380A (en) * 1996-03-01 2000-12-26 Neste Oy Method for transferring heat utilizing heat transfer/cooling fluid having tri-methyl glycine
US6436385B2 (en) 1996-09-26 2002-08-20 Cultor Corporation Preparation protecting skin from mechanical irritation
WO2003030992A1 (en) * 2001-10-04 2003-04-17 Beiersdorf Ag Betaine-containing cosmetics
JP2005029532A (en) * 2003-07-09 2005-02-03 Asahi Kasei Chemicals Corp Skin-cleansing agent

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6165380A (en) * 1996-03-01 2000-12-26 Neste Oy Method for transferring heat utilizing heat transfer/cooling fluid having tri-methyl glycine
US6436385B2 (en) 1996-09-26 2002-08-20 Cultor Corporation Preparation protecting skin from mechanical irritation
US6156293A (en) * 1997-01-03 2000-12-05 Finnfedds Finland Ltd. Moistening preparation
JPH11217211A (en) * 1998-01-30 1999-08-10 Shiseido Co Ltd Sol composition
WO2003030992A1 (en) * 2001-10-04 2003-04-17 Beiersdorf Ag Betaine-containing cosmetics
JP2005029532A (en) * 2003-07-09 2005-02-03 Asahi Kasei Chemicals Corp Skin-cleansing agent

Also Published As

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