JPH11116436A - Preparation for external use for skin - Google Patents

Preparation for external use for skin

Info

Publication number
JPH11116436A
JPH11116436A JP9297860A JP29786097A JPH11116436A JP H11116436 A JPH11116436 A JP H11116436A JP 9297860 A JP9297860 A JP 9297860A JP 29786097 A JP29786097 A JP 29786097A JP H11116436 A JPH11116436 A JP H11116436A
Authority
JP
Japan
Prior art keywords
skin
external preparation
component
present
acid
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.)
Withdrawn
Application number
JP9297860A
Other languages
Japanese (ja)
Inventor
Tetsuya Sakai
哲也 境
Nao Maruyama
菜生 丸山
Keiichi Uchikawa
恵一 内川
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.)
Shiseido Co Ltd
Original Assignee
Shiseido 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 Shiseido Co Ltd filed Critical Shiseido Co Ltd
Priority to JP9297860A priority Critical patent/JPH11116436A/en
Publication of JPH11116436A publication Critical patent/JPH11116436A/en
Withdrawn legal-status Critical Current

Links

Landscapes

  • Medicinal Preparation (AREA)
  • Cosmetics (AREA)
  • Medicines Containing Plant Substances (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a preparation for external use for skin that contains erythritol, an anti-inflammatory component and an antimicrobial agent, manifests excellent pimple treatment effect with mild action on the skin and no hormone- like side effect and is useful for treatment of acne. SOLUTION: This preparation for external use for skin comprises (A) 0.01-10.0 wt.% of erythritol, (B) an anti-inflammatory component, in an amount of 0.0001-10.0 wt.%, when glycyrrhizic acid is used as the component B, and (C) an antimicrobial agent, in an amount of 0.001-10.0 wt.%, when cork tree bark is used as the component C. When necessary, this preparation can contain, in addition, a compound having sebum-suppressing effect such as vitamin B6 , an astringent agent such as sodium phenol-sulfate, pharmaceutical components such as vitamin A acid (or its derivative), salicylic acid, zinc or its compounds, lactic acid and the like, a keratolytic drug and a moisture retainer such as hyarulonic acid and the like.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明はニキビ治療効果に優
れた皮膚外用剤に関する。
The present invention relates to an external preparation for skin which is excellent in treating acne.

【0002】[0002]

【従来の技術】ニキビは主として思春期に発現する皮膚
疾患で、その正式な病名を尋常性座瘡といい、臨床的に
は“毛嚢脂腺系を中心に毛孔に起こる慢性の炎症性変
化”と定義されている。その発症病理はいまだ不明な点
が多いが、一般には皮脂分泌過剰,毛嚢角化,毛嚢内細
菌が重要な役割を果たしつつ、種々の要因が複雑に絡み
合っている皮膚疾患であると考えられている。従って、
ニキビ治療用の外用剤としては、上記の各要因に対応し
て、皮脂分泌抑制成分、角質溶解成分、消炎成分及び/
又は抗菌物質を配合したクリームや軟膏が一般に多く用
いられている。
2. Description of the Related Art Acne is a skin disease that mainly develops during puberty, and its formal name is acne vulgaris. Clinically, "acne acne is a chronic inflammatory change that occurs in pores mainly in the pilosebaceous system. Is defined. Although the pathogenesis is still largely unknown, it is generally considered to be a skin disease in which various factors are intricately intertwined while hypersecretion of sebum, keratinization of hair follicles, and bacteria in hair follicles play important roles. ing. Therefore,
External preparations for treating acne include sebum secretion inhibiting components, keratolytic components, anti-inflammatory components and / or
Or creams and ointments containing an antibacterial substance are generally used in many cases.

【0003】[0003]

【発明が解決しようとする課題】しかし、上記の各種成
分を配合した既存のニキビ治療薬においても種々の欠点
が報告されている。例えば、皮脂分泌抑制成分である女
性ホルモンは、表皮の成長を抑制し皮脂の分泌を減少さ
せるが、この種のホルモンがひきおこす副作用は、特に
思春期の男女には好ましいものではない。また、皮脂抑
制作用を有する塩酸ピリドキシンやシャクヤクエキス,
ゴボウエキスといった生薬類は単独でクリームや軟膏等
に配合しても十分な皮脂抑制効果はみられず、ニキビ治
療の効果は必ずしも十分なものではなかった。さらに、
角質溶解成分の代表例である硫黄や二硫化セレン等の硫
黄化合物は、上記の女性ホルモンのような副作用は認め
られないが、連用することにより皮膚刺激や皮膚のかさ
つき等を起こす場合が多い。
However, various drawbacks have also been reported in existing acne remedies containing the various components described above. For example, female hormones, which are sebum secretion inhibiting components, suppress epidermal growth and reduce sebum secretion, but the side effects caused by these hormones are not particularly favorable for adolescent men and women. In addition, pyridoxine hydrochloride and peony extract, which have sebum-suppressing action,
Crude drugs such as burdock extract alone did not show a sufficient sebum-suppressing effect even when incorporated in creams or ointments, etc., and the effect of acne treatment was not always sufficient. further,
Sulfur compounds such as sulfur and selenium disulfide, which are typical examples of the keratolytic components, do not have side effects like the female hormones described above, but often cause skin irritation and skin bulking when used continuously.

【0004】本発明の目的は、かかる事情に鑑み、ホル
モン様の副作用を有さず、皮膚に対して温和で、かつニ
キビ治療効果に優れたニキビ治療用の皮膚外用剤を提供
することにある。
[0004] In view of such circumstances, an object of the present invention is to provide a skin external preparation for acne treatment which has no hormonal side effects, is mild to the skin, and has an excellent acne treatment effect. .

【0005】[0005]

【課題を解決するための手段】そこで、本発明者は上記
課題を解決すべく鋭意検討を重ねた結果、エリスリトー
ルと消炎成分並びに抗菌成分を配合した皮膚外用剤は、
皮膚に対して温和で、さらに異常角化を抑え、ニキビ治
療の目的を良好に達成することを見出し、本発明を完成
するに至った。
The inventors of the present invention have made intensive studies to solve the above-mentioned problems, and as a result, an external preparation for skin containing erythritol, an anti-inflammatory component and an antibacterial component has been developed.
The present inventors have found that the present invention is gentle on the skin, further suppresses abnormal keratinization, and satisfactorily achieves the purpose of acne treatment, thereby completing the present invention.

【0006】すなわち、本発明の第1は、エリスリトー
ル、消炎成分および抗菌成分を配合することを特徴とす
る皮膚外用剤である。本発明の第2は、エリスリトー
ル、消炎成分および抗菌成分を配合することを特徴とす
るニキビ治療用皮膚外用剤である。本発明の第3は、エ
リスリトール、消炎成分および抗菌成分からなることを
特徴とするニキビ治療剤である。なお、本発明において
消炎成分としてはグリチルリチン酸またはその誘導体が
好ましく、抗菌成分としてはオウバク抽出液が好まし
い。
[0006] That is, a first aspect of the present invention is a skin external preparation characterized by containing erythritol, an anti-inflammatory component and an antibacterial component. The second aspect of the present invention is an external preparation for acne treatment, which comprises erythritol, an anti-inflammatory component and an antibacterial component. A third aspect of the present invention is a remedy for acne comprising erythritol, an anti-inflammatory component and an antibacterial component. In the present invention, glycyrrhizic acid or a derivative thereof is preferable as the anti-inflammatory component, and oak extract is preferable as the antibacterial component.

【0007】以下、本発明の実施の形態について説明す
る。本発明において用いられるエリスリトールはメソ−
エリスリトールとも呼ばれ、天然界では地衣類、担子
菌、果実などに含まれる4炭糖の糖アルコールである。
以前より高い保湿効果を有することが知られており、化
粧料等に応用されているが、本発明のように抗炎症剤と
抗菌成分との組み合わせにおいて高いニキビ治療効果を
有することは知られていない。
Hereinafter, embodiments of the present invention will be described. Erythritol used in the present invention is meso-
Also called erythritol, it is a 4-carbon sugar alcohol contained in lichens, basidiomycetes, fruits and the like in the natural world.
It is known that it has a higher moisturizing effect than before, and it is applied to cosmetics and the like, but it is known that a combination of an anti-inflammatory agent and an antibacterial component has a high acne treatment effect as in the present invention. Absent.

【0008】本発明皮膚外用剤に有効成分として配合可
能なエリスリトールの配合量は、皮膚外用剤全体に対し
て0.01重量%以上,10.0重量%以下が好まし
く、0.1重量%以上,5.0重量%以下が特に好まし
い。エリスリトールの配合量が皮膚外用剤全体に対して
0.01重量%未満では所望する効果が発揮され難い故
に好ましくなく、同10.0重量%を超えるとべたつき
が顕著になり製剤上好ましくなく、配合量に見合ったニ
キビ抑制効果の増大が認められない傾向にもなり好まし
くない。
[0008] The amount of erythritol which can be incorporated as an active ingredient in the skin external preparation of the present invention is preferably 0.01% by weight or more and 10.0% by weight or less, and more preferably 0.1% by weight or less based on the whole skin external preparation. , 5.0% by weight or less is particularly preferred. If the amount of erythritol is less than 0.01% by weight based on the total amount of the external preparation for skin, it is not preferable because the desired effect is hardly exhibited, and if it exceeds 10.0% by weight, stickiness becomes remarkable and the formulation is not preferred. It is not preferable because the acne suppression effect corresponding to the amount tends not to increase.

【0009】また、本発明皮膚外用剤に配合可能な消炎
成分としては、炎症を抑えるという機能を有し、かつ皮
膚外用剤の配合成分として安全性等の面で適切であれば
特に限定されるものではない。
The anti-inflammatory component that can be incorporated into the external preparation for skin of the present invention is not particularly limited as long as it has a function of suppressing inflammation and is appropriate as a component of the external preparation for skin in terms of safety and the like. Not something.

【0010】具体的には、従来より消炎成分として用い
られている成分、例えばアラントイン,グリチルリチン
酸(塩),グリチルレチン酸またはその誘導体,グルタ
チオン,アシルサルコシン酸,甘草抽出成分,黄連抽出
成分,シコン抽出成分,西洋ノコギリ草抽出成分,ヒリ
ハリ草抽出成分,アロエ抽出成分,ギシギシ抽出成分,
コウホネ抽出成分,ゼニアオイ抽出成分,トウキ抽出成
分,スギナ抽出成分,ユキノシタ抽出成分,アルニカ抽
出成分,ユリ属植物の抽出成分,ヨモギ抽出成分,クチ
ナシ抽出成分、カミツレ抽出成分等を挙げることができ
る。
[0010] Specifically, components conventionally used as anti-inflammatory components, such as allantoin, glycyrrhizic acid (salt), glycyrrhetinic acid or a derivative thereof, glutathione, acyl sarcosine acid, licorice extract component, orchid extract component, and sicon Extract component, Western saw grass extract component, Hilihari grass extract component, Aloe extract component, Rigix japonicus extract component,
Examples of the components include a corn extract, a mallow extract, a corn extract, a horsetail extract, a saxifrage extract, an arnica extract, a lily plant extract, a mugwort extract, a gardenia extract, and a chamomile extract.

【0011】なお、本発明皮膚外用剤に配合する消炎成
分としては、安定性及び使用性に特に優れるという点に
おいてグリチルリチン酸またはその誘導体が特に好まし
い。
Glycyrrhizic acid or a derivative thereof is particularly preferred as an anti-inflammatory component to be added to the external preparation for skin of the present invention, because it is particularly excellent in stability and usability.

【0012】また、これらの消炎成分は、単独で本発明
皮膚外用剤中に配合することも可能であるが、必要に応
じて2種以上を組み合わせて本発明皮膚外用剤中に配合
することも可能である。
These anti-inflammatory components can be used alone in the external preparation for skin of the present invention, but if necessary, two or more of them can be combined in the external preparation for skin of the present invention. It is possible.

【0013】本発明皮膚外用剤における上記の消炎成分
の配合量は、具体的に配合する消炎成分の種類に応じて
適宜調整可能であり、特に限定されるものではない。例
えば、本発明皮膚外用剤に配合するのに好適なグリチル
リチン酸またはその塩の場合は、皮膚外用剤全体に対し
て0.0001重量%以上,10.0重量%以下が好ま
しく、同0.01重量%以上,5.0重量%以下が特に
好ましい。この場合、配合量が皮膚外用剤全体に対して
0.0001重量%未満では、所望する消炎効果が発揮
され難い故に好ましくなく、同10.0重量%を超える
と配合量に見合った消炎効果の増大が認められない傾向
になり好ましくない。
The amount of the anti-inflammatory component in the external preparation for skin of the present invention can be appropriately adjusted according to the type of the anti-inflammatory component to be specifically mixed, and is not particularly limited. For example, in the case of glycyrrhizic acid or a salt thereof suitable for being incorporated into the external preparation for skin of the present invention, the amount is preferably 0.0001% by weight or more and 10.0% by weight or less, and 0.01% by weight or less based on the whole external preparation for skin. It is particularly preferable that the content be not less than 5.0% by weight and not more than 5.0% by weight. In this case, if the amount is less than 0.0001% by weight based on the total amount of the external preparation for skin, it is not preferable because the desired anti-inflammatory effect is hardly exhibited. If the amount exceeds 10.0% by weight, the anti-inflammatory effect corresponding to the amount is not sufficient. It is not preferable because no increase is observed.

【0014】さらに、本発明皮膚外用剤に配合可能な抗
菌成分としては、アクネ菌の生育を抑えるという機能を
有し、かつ皮膚外用剤の配合成分として安全性等の面で
適切であれば特に限定されるものではない。
Further, the antibacterial component which can be added to the external preparation for skin of the present invention may be any antibacterial component as long as it has a function of suppressing the growth of acne bacteria and is suitable as a component of the external preparation for skin in terms of safety and the like. It is not limited.

【0015】具体的には、従来より抗菌成分としてニキ
ビを抑制する目的に用いられている成分、例えば、オウ
バク抽出液、ヒノキチオール、トリクロサン、トリクロ
ロカルバニリド、クロルヘキシジン塩酸塩、クロルヘキ
シジングルコンサン塩、ハロカルバン、クロロフェネシ
ン、塩化ベンゼトニウム、塩化ベンザルコニウム、塩化
リゾチーム、塩酸アルキルジアミノエチルグリシン、イ
ソプロピルメチルフェノール、安息香酸、感光素201
号、チモール、ヘキサクロロフェン、ベルベリン、チオ
キソロン、サリチル酸およびそれらの誘導体を挙げるこ
とができる。
Specifically, components conventionally used for controlling acne as antibacterial components, for example, oak extract, hinokitiol, triclosan, trichlorocarbanilide, chlorhexidine hydrochloride, chlorhexidine glucoconsan salt, halo Carbane, chlorophenesin, benzethonium chloride, benzalkonium chloride, lysozyme chloride, alkyldiaminoethylglycine hydrochloride, isopropylmethylphenol, benzoic acid, photosensitizer 201
No., thymol, hexachlorophen, berberine, thioxolone, salicylic acid and derivatives thereof.

【0016】なお、本発明皮膚外用剤に配合する抗菌成
分としては、安定性及び使用性に特に優れるという点に
おいてオウバク抽出液が特に好ましい。
As an antibacterial component to be added to the external preparation for skin of the present invention, oak extract is particularly preferable in that it is particularly excellent in stability and usability.

【0017】また、これらの抗菌成分は、単独で本発明
皮膚外用剤中に配合することも可能であるが、必要に応
じて2種以上を組み合わせて本発明皮膚外用剤中に配合
することも可能である。
These antimicrobial components can be used alone in the external preparation for skin of the present invention. However, if necessary, two or more of them can be combined in the external preparation for skin of the present invention. It is possible.

【0018】本発明皮膚外用剤における上記の抗菌成分
の配合量は、具体的に配合する抗菌成分の種類に応じて
適宜調整可能であり、特に限定されるものではない。例
えば、本発明皮膚外用剤に配合するのに好適なオウバク
抽出液の場合は、皮膚外用剤全体に対して0.0001
重量%以上,10.0重量%以下が好ましく、同0.0
1重量%以上,5.0重量%以下が特に好ましい。この
場合、配合量が皮膚外用剤全体に対して0.0001重
量%未満では、所望する抗菌効果が発揮され難い故に好
ましくなく、同10.0重量%を超えると配合量に見合
った抗菌効果の増大が認められない傾向になり好ましく
ない。
The amount of the above antibacterial component in the external preparation for skin of the present invention can be appropriately adjusted according to the type of the antibacterial component to be concretely added, and is not particularly limited. For example, in the case of an oak extract suitable for blending with the external preparation for skin of the present invention, 0.0001 with respect to the whole external preparation for skin.
% By weight and not more than 10.0% by weight.
Particularly preferred is 1% by weight or more and 5.0% by weight or less. In this case, if the amount is less than 0.0001% by weight based on the total amount of the external preparation for skin, the desired antibacterial effect is hardly exhibited, so that it is not preferable. It is not preferable because no increase is observed.

【0019】このように、エリスリトールと消炎成分と
抗菌成分とを有効成分として組み合わせて配合すること
により、皮膚に対して温和で、しかも角化異常を抑制す
ることができるニキビ治療用の皮膚外用剤が提供され
る。
As described above, by combining erythritol, an anti-inflammatory component and an antibacterial component in combination as active ingredients, an external preparation for acne treatment which is mild on the skin and can suppress abnormal keratinization. Is provided.

【0020】また、上記の必須の有効成分に加えて、他
の薬効成分を、本発明の所期の効果を損なわない範囲
で、またその薬効成分を皮膚外用剤中に配合することで
発揮される効果が予測される範囲内で本発明皮膚外用剤
中に配合することができる。
Further, in addition to the above-mentioned essential active ingredients, other medicinal ingredients are exerted by blending the medicinal ingredients in a skin external preparation within a range not to impair the intended effect of the present invention. Within the range in which the effect is expected.

【0021】例えば、ビタミンB6等の皮脂抑制効果を
有する化合物、スルフォ石炭酸ソーダ等の収斂剤、ビタ
ミンA酸及びその誘導体、サリチル酸、亜鉛及びその化
合物、乳酸等の薬効成分を本発明皮膚外用剤中に配合す
ることができる。また、角質溶解剤やヒアルロン酸等の
保湿剤を本発明皮膚外用剤中に配合することができる。
For example, a compound having a sebum-suppressing effect such as vitamin B6, an astringent such as sodium sulfocarbonate, vitamin A acid and its derivatives, salicylic acid, zinc and its compounds, and lactic acid and other medicinal ingredients are contained in the skin external preparation of the present invention. Can be blended. In addition, a humectant such as a keratolytic agent or hyaluronic acid can be incorporated into the external preparation for skin of the present invention.

【0022】なお、本発明皮膚外用剤中に配合可能な
「他の薬剤等」が、ここに例示したものに限定されるも
のではないこと、及びこれらの「他の薬剤等」を1種の
みならず、必要に応じて2種以上を組み合わせて本発明
皮膚外用剤中に配合可能であることは勿論である。
It should be noted that the "other drugs and the like" that can be incorporated into the external preparation for skin of the present invention are not limited to those exemplified here, and that only one of these "other drugs and the like" is used. It is needless to say that two or more kinds can be combined in the external preparation for skin of the present invention as needed.

【0023】また、本発明皮膚外用剤の具体的な剤型及
び形態に応じて、通常公知の基剤成分等を、本発明皮膚
外用剤の基剤成分等として用いることができる。すなわ
ち、各種油分,界面活性剤,水,エタノール,増粘剤,
香料,色素等を本発明の所期の効果を損なわない範囲で
本発明皮膚外用剤の基剤成分等として用いることができ
る。
In addition, depending on the specific dosage form and form of the external preparation for skin of the present invention, generally known base components and the like can be used as the base components and the like of the external preparation for skin of the present invention. That is, various oils, surfactants, water, ethanol, thickeners,
Fragrances, pigments and the like can be used as a base component and the like of the external preparation for skin of the present invention as long as the desired effects of the present invention are not impaired.

【0024】なお、本発明皮膚外用剤がとり得る剤型は
特に限定されず、クリーム,ローション,乳液,パッ
ク,白粉,軟膏等外皮に適用できるものであればいずれ
も選択することができる。
The form that the external preparation for skin of the present invention can take is not particularly limited, and any form such as cream, lotion, emulsion, pack, white powder, ointment and the like that can be applied to the outer skin can be selected.

【0025】[0025]

【実施例】次に実施例等を挙げて、本発明をさらに具体
的に説明するが、本発明はこれにより限定されるもので
はない。また、配合量は特に断らない限り、皮膚外用剤
全体に対する重量%である。実施例に先立ち、本発明皮
膚外用剤の評価をするために用いた試験法・基準を記載
する。
EXAMPLES Next, the present invention will be described more specifically with reference to examples and the like, but the present invention is not limited thereto. Unless otherwise specified, the compounding amount is% by weight based on the whole skin external preparation. Prior to the examples, test methods and criteria used for evaluating the skin external preparation of the present invention will be described.

【0026】試験法・基準 (使用薬剤)後述する各々の皮膚外用剤の処方に基づ
き、常法によって製造した皮膚外用剤のニキビ抑制効果
を測定した。
Test Methods / Criteria (Drugs Used) Based on the formulation of each skin external preparation described below, the acne-suppressing effect of a skin external preparation manufactured by an ordinary method was measured.

【0027】(使用対象)13才から20才までのニキ
ビに悩む男女120名。(1群20名) (使用方法および観察日)化粧石鹸を用いて顔面をよく
洗浄した後、皮疹上にのみ各々の皮膚外用剤を1日に2
〜3回塗布して、4週間後に患部の観察を行った。
(Used) 120 men and women between the ages of 13 and 20 suffering from acne. (20 people per group) (Method of use and date of observation) After thoroughly washing the face with toilet soap, each topical skin preparation was applied only on the rash 2 times a day.
塗布 3 times and the affected area was observed 4 weeks later.

【0028】(全般改善度)使用前に比較して使用薬剤
により症状が改善されたことを示す(a)、不変又は悪
化したことを示す(b)の2段階に分けた。 (有用性の評価) 全般改善度で次のように評価した。 ◎:20名中(a)が15名以上 ○:20名中(a)が10〜14名 △:20名中(a)が5〜9名 ×:20名中(a)が4名以下
(Overall degree of improvement) The symptoms were divided into two stages: (a) indicating that the symptom was improved by the drug used before use, and (b) indicating that the condition was unchanged or worsened. (Evaluation of usefulness) The overall improvement was evaluated as follows. ◎: 15 or more out of 20 (a) ○: 10 to 14 out of 20 (a) △: 5 to 9 out of 20 (a) ×: 4 or less out of 20 (a)

【0029】実施例1、比較例1〜4 表1に示した処方のローションタイプの皮膚外用剤を調
製して、上記の手法によりその有用性を評価した。この
結果を併せて表1に記載する。
Example 1, Comparative Examples 1-4 A lotion-type skin external preparation having the formulation shown in Table 1 was prepared, and its usefulness was evaluated by the above method. The results are shown in Table 1.

【0030】[0030]

【表1】 ────────────────────────────── 実施例 比較例 成分/試料名 ──── ──────────── 1 1 2 3 4 ────────────────────────────── エリスリトール 1.0 − 1.0 − − グリチルリチン酸ジカリウム 0.1 − − 0.1 − オウバク抽出液 0.05 − − − 0.05 ソルビトール(70%) 3.0 3.0 3.0 3.0 3.0 グリセリン 5.0 5.0 5.0 5.0 5.0 POE(60)硬化ヒマシ油誘導体 0.5 0.5 0.5 0.5 0.5 エタノール 20.0 20.0 20.0 20.0 20.0 精製水 残余 残余 残余 残余 残余 ────────────────────────────── 有用性 ◎ × △ △ △ ──────────────────────────────[Table 1] 例 Example Comparative example Component / sample name 試 料 ──── ──────── 1 1 2 3 4 ────────────────────────────── Erythritol 1.0-1.0--Glycyrrhizin Dipotassium acid 0.1 − − 0.1 − Oak extract 0.05 − − − 0.05 Sorbitol (70%) 3.0 3.0 3.0 3.0 3.0 Glycerin 5.0 5.0 5.0 5.0 5.0 POE (60) hydrogenated castor oil derivative 0.5 0.5 0.5 0.5 0.5 Ethanol 20.0 20.0 20.0 20.0 20.0 Purified water Residue Residue Residue Residue Residue ────────────────────────────── Utility ◎ × △ △ △ ────── ────────────────────────

【0031】表1に示すように、エリスリトールと、消
炎成分としてグリチルリチン酸ジカリウム、抗菌成分と
してオウバク抽出液を配合した本発明の皮膚外用剤は、
各比較例のローションに比べニキビ抑制効果に優れてい
る。
As shown in Table 1, the external preparation for skin of the present invention comprising erythritol, dipotassium glycyrrhizinate as an anti-inflammatory component, and oak extract as an antibacterial component,
It is more excellent in acne suppression effect than the lotion of each comparative example.

【0032】以下に、種々の剤型の本発明皮膚外用剤の
処方例を示すが、各実施例の本発明皮膚外用剤も、その
具体的な剤型に応じた常法により製造した。また、各実
施例の本発明皮膚外用剤に上記の試験・評価を施したと
ころ、全て上記の有用性評価結果は「◎」であった。
Formulation examples of the external preparation for skin of the present invention in various dosage forms are shown below. The external preparation for skin of the present invention in each Example was also produced by a conventional method corresponding to the specific dosage form. When the above-mentioned tests and evaluations were performed on the skin external preparations of the present invention in each of the examples, all the above-mentioned evaluation results of the usefulness were “性”.

【0033】 実施例3 ローション 配合量(重量%) (1) エリスリトール 0.5 (2) グリチルリチン酸ジカリウム 0.05 (3) オウバクエキス 0.1 (4) スルフォ石炭酸ソーダ 0.05 (5) グリセリン 4.0 (6) 1,3−ブチレングリコール 4.0 (7) エタノール 7.0 (8) ポリオキシエチレンオレイルアルコール 0.5 (9) メチルパラベン 0.05 (10)クエン酸 0.01 (11)クエン酸ソーダ 0.1 (12)香料 0.05 (13)精製水 残余Example 3 Lotion Compounding Amount (% by Weight) (1) Erythritol 0.5 (2) Dipotassium glycyrrhizinate 0.05 (3) Oubaku Extract 0.1 (4) Sulfolite Sodium Carbonate 0.05 (5) Glycerin 4.0 (6) 1,3-butylene glycol 4.0 (7) Ethanol 7.0 (8) Polyoxyethylene oleyl alcohol 0.5 (9) Methylparaben 0.05 (10) Citric acid 0.01 (11 ) Sodium citrate 0.1 (12) Fragrance 0.05 (13) Purified water residue

【0034】 実施例4 クリーム 配合量(重量%) (1) セトステアリルアルコール 3.5 (2) スクワラン 40.0 (3) ミツロウ 3.0 (4) 還元ラノリン 5.0 (5) エチルパラベン 0.3 (6) ポリオキシエチレン(20) ソルビタンモノパルミチン酸エステル 2.0 (7) ステアリン酸モノグリセリド 2.0 (8) 香料 0.03 (9) エリスリトール 5.0 (10)アラントイン 0.1 (11)ヒノキチオール 0.05 (12)1,3−ブチレングリコール 5.0 (13)グリセリン 5.0 (14)精製水 残余Example 4 Cream Content (% by Weight) (1) Cetostearyl Alcohol 3.5 (2) Squalane 40.0 (3) Beeswax 3.0 (4) Reduced Lanolin 5.0 (5) Ethyl Paraben 0 0.3 (6) polyoxyethylene (20) sorbitan monopalmitate 2.0 (7) stearic acid monoglyceride 2.0 (8) fragrance 0.03 (9) erythritol 5.0 (10) allantoin 0.1 ( 11) Hinokitiol 0.05 (12) 1,3-butylene glycol 5.0 (13) Glycerin 5.0 (14) Purified water residue

【0035】 実施例5 乳液 配合量(重量%) (1) エリスリトール 1.0 (2) カミツレエキス 0.1 (3) 安息香酸 0.1 (4) ステアリン酸 1.5 (5) セチルアルコール 0.5 (6) ミツロウ 2.0 (7) ポリオキシエチレン(10)モノオレイン酸エステル 1.0 (8) グリセリンモノステアリン酸エステル 1.0 (9) プロピレングリコール 5.0 (10)エタノール 3.0 (11)エチルパラベン 0.3 (12)香料 0.03 (13)精製水 残余Example 5 Emulsion Compounding amount (% by weight) (1) Erythritol 1.0 (2) Chamomile extract 0.1 (3) Benzoic acid 0.1 (4) Stearic acid 1.5 (5) Cetyl alcohol 0 2.5 (6) Beeswax 2.0 (7) Polyoxyethylene (10) monooleate 1.0 (8) Glycerin monostearate 1.0 (9) Propylene glycol 5.0 (10) Ethanol 3. 0 (11) Ethyl paraben 0.3 (12) Fragrance 0.03 (13) Purified water residue

【0036】 実施例6 軟膏 配合量(重量%) (1) エリスリトール 2.0 (2) グリチルレチン酸 0.1 (3) サリチル酸 0.1 (4) ステアリルアルコール 18.0 (5) モクロウ 20.0 (6) ポリオキシエチレン(10)モノオレイン酸エステル 0.25 (7) グリセリンモノステアリン酸エステル 0.25 (8) ワセリン 40.0 (9) 精製水 残 余 Example 6 Ointment Compounding amount (% by weight) (1) Erythritol 2.0 (2) Glycyrrhetinic acid 0.1 (3) Salicylic acid 0.1 (4) Stearyl alcohol 18.0 (5) Mokurou 20.0 (6) Polyoxyethylene (10) monooleate 0.25 (7) Glycerin monostearate 0.25 (8) Vaseline 40.0 (9) Purified water residue

【0037】[0037]

【発明の効果】以上説明したように、本発明によれば皮
膚に対して温和で、かつ優れたニキビ治療効果を有する
皮膚外用剤を提供することが可能となる。
As described above, according to the present invention, it is possible to provide an external preparation for skin that is mild to the skin and has an excellent acne treatment effect.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI A61K 9/06 A61K 9/06 G 35/78 ADA 35/78 ADAW ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 6 Identification code FI A61K 9/06 A61K 9/06 G 35/78 ADA 35/78 ADAW

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 エリスリトール、消炎成分および抗菌成
分を配合することを特徴とする皮膚外用剤。
1. An external preparation for skin, comprising erythritol, an anti-inflammatory component and an antibacterial component.
【請求項2】 消炎成分がグリチルリチン酸またはその
誘導体である請求項1記載の皮膚外用剤。
2. The external preparation for skin according to claim 1, wherein the anti-inflammatory component is glycyrrhizic acid or a derivative thereof.
【請求項3】 抗菌成分がオウバク抽出液である請求項
1または2記載の皮膚外用剤。
3. The external preparation for skin according to claim 1, wherein the antibacterial component is an extract of oak.
【請求項4】 皮膚外用剤がニキビ治療用皮膚外用剤で
ある請求項1〜3のいずれかに記載の皮膚外用剤。
4. The external preparation for skin according to claim 1, wherein the external preparation for skin is an external preparation for acne treatment.
【請求項5】 エリスリトール、消炎成分および抗菌成
分からなることを特徴とするニキビ治療剤。
5. A therapeutic agent for acne, comprising erythritol, an anti-inflammatory component and an antibacterial component.
JP9297860A 1997-10-15 1997-10-15 Preparation for external use for skin Withdrawn JPH11116436A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9297860A JPH11116436A (en) 1997-10-15 1997-10-15 Preparation for external use for skin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9297860A JPH11116436A (en) 1997-10-15 1997-10-15 Preparation for external use for skin

Publications (1)

Publication Number Publication Date
JPH11116436A true JPH11116436A (en) 1999-04-27

Family

ID=17852089

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9297860A Withdrawn JPH11116436A (en) 1997-10-15 1997-10-15 Preparation for external use for skin

Country Status (1)

Country Link
JP (1) JPH11116436A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1358872A1 (en) * 2002-04-30 2003-11-05 Cognis Iberia, S.L. Use of mixtures of active compounds comprising azelaic acid and glycyrrhetic acid in the treatment of acne
JP2011098901A (en) * 2009-11-05 2011-05-19 Noevir Co Ltd Skin care preparation for acne
US11517578B1 (en) * 2021-07-29 2022-12-06 Innomed Technologies, Inc. Topical formulations containing erythritol and methods of treating skin conditions

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1358872A1 (en) * 2002-04-30 2003-11-05 Cognis Iberia, S.L. Use of mixtures of active compounds comprising azelaic acid and glycyrrhetic acid in the treatment of acne
WO2003092655A3 (en) * 2002-04-30 2004-04-15 Cognis Iberia Sl Use of active ingredient mixtures with azelaic acids and glycyrrhetic acids as anti-acne agents
JP2011098901A (en) * 2009-11-05 2011-05-19 Noevir Co Ltd Skin care preparation for acne
US11517578B1 (en) * 2021-07-29 2022-12-06 Innomed Technologies, Inc. Topical formulations containing erythritol and methods of treating skin conditions
WO2023009829A1 (en) * 2021-07-29 2023-02-02 Innomed Technologies, Inc. Topical formulations containing erythritol and methods of treating skin conditions

Similar Documents

Publication Publication Date Title
KR101420599B1 (en) Compositions containing anti-acne agents and the use thereof
JPS59108716A (en) Antiacne composition
JP2000169321A (en) Cell activation agent and preparation for external use for skin and skin cleaning agent containing the activation agent
US20110236503A1 (en) Topical Skincare Composition
US8513225B2 (en) Composition and method for topical treatment of skin lesions
US20040247633A1 (en) Novel dermatological composition
JP2003238379A (en) Skin care preparation and hair cosmetic
JPH09157172A (en) Skin external agent and treating agent for eczema
JP2878353B2 (en) External preparation for skin
JP2007332078A (en) Agent for external use containing ozone-dissolved glycerol solution such as cosmetic, quasi-drug or medicament (pharmaceutical)
US5886038A (en) Composition and method for treatment of psoriasis
JPH11100324A (en) Composition for treating pimple
JPH11116436A (en) Preparation for external use for skin
JPH11269043A (en) Cosmetic for scalp and hair
JP4669595B2 (en) External agent for preventing and treating acne vulgaris and cosmetics containing the external agent
JPS63188628A (en) Drug for skin external use
JPH10265365A (en) External preparation for skin for pimple
JP2781982B2 (en) External preparation for skin
JP3421071B2 (en) External preparation containing oil-soluble licorice extract
JPH11302133A (en) Cosmetic for scalp and hair
JP3582951B2 (en) External preparation for skin
JP3516792B2 (en) External preparation for skin
JP2003113070A (en) Stabilizer for oil-soluble licorice extract and method of stabilizing the same
JPH0640858A (en) Hair tonic
JP2826141B2 (en) Dandruff inhibitor composition

Legal Events

Date Code Title Description
A300 Withdrawal of application because of no request for examination

Free format text: JAPANESE INTERMEDIATE CODE: A300

Effective date: 20050104