JP2542849B2 - Topical skin - Google Patents

Topical skin

Info

Publication number
JP2542849B2
JP2542849B2 JP62140658A JP14065887A JP2542849B2 JP 2542849 B2 JP2542849 B2 JP 2542849B2 JP 62140658 A JP62140658 A JP 62140658A JP 14065887 A JP14065887 A JP 14065887A JP 2542849 B2 JP2542849 B2 JP 2542849B2
Authority
JP
Japan
Prior art keywords
skin
extract
present
effect
external preparation
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.)
Expired - Lifetime
Application number
JP62140658A
Other languages
Japanese (ja)
Other versions
JPS63303909A (en
Inventor
千春 渡辺
伊都子 西川
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.)
KOSEI KK
Original Assignee
KOSEI KK
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 KOSEI KK filed Critical KOSEI KK
Priority to JP62140658A priority Critical patent/JP2542849B2/en
Publication of JPS63303909A publication Critical patent/JPS63303909A/en
Application granted granted Critical
Publication of JP2542849B2 publication Critical patent/JP2542849B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/004Aftersun preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
    • A61K8/9783Angiosperms [Magnoliophyta]
    • A61K8/9789Magnoliopsida [dicotyledons]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、新規な皮膚外用剤に関し、さらに詳しく
は、イブキトラノオ抽出物を含有することを特徴とす
る、皮膚の炎症を防止・緩和する皮膚外用剤に関するも
のである。
TECHNICAL FIELD The present invention relates to a novel external preparation for skin, more specifically, it prevents or alleviates skin inflammation, which is characterized by containing an extract of Ibuquitranoo. It relates to a skin external preparation.

本発明の目的とするところは、日焼け・肌荒れ・外傷
・にきび等による皮膚の炎症を防止・緩和する、肌荒れ
防止効果、肌荒れ改善効果に優れた皮膚外用剤に関す
る。
The object of the present invention is to provide a skin external preparation which is excellent in the effect of preventing skin roughness and the effect of improving skin roughness, which prevents and relieves inflammation of the skin due to sunburn, rough skin, trauma, acne and the like.

[従来の技術] 従来、抗炎症作用を有する植物抽出物として、甘草、
黄柏、紫根等の種々のものが知られており、肌荒れ防
止、肌荒れ改善効果を期待して、これらを皮膚外用剤に
配合する試みがなされてきた。
[Prior Art] Conventionally, as a plant extract having an anti-inflammatory effect, licorice,
Various materials such as yellow oak and purple root are known, and attempts have been made to blend them into an external preparation for skin in the hope of preventing rough skin and improving rough skin.

[発明が解決しようとする問題点] しかしながら、従来使用されてきた植物抽出物では、
有効な肌荒れ改善効果を有するものは限られていた。
[Problems to be Solved by the Invention] However, in the plant extracts that have been conventionally used,
Those having an effective effect of improving rough skin have been limited.

[問題点を解決するための手段] 本発明者等は、係る点に鑑み、種々の植物抽出物につ
いて鋭意研究した結果、イブキトラノオ抽出物が優れた
抗炎症作用を有し、かつこれを含有する皮膚外用剤にお
いても顕著な肌荒れ防止効果が得られることを見出し、
本発明を完成させたのである。
[Means for Solving the Problems] In view of the above points, the present inventors have conducted diligent research on various plant extracts, and as a result, the Ibuquitranoo extract has an excellent anti-inflammatory action and contains it. It was found that even in the external preparation for skin, a remarkable effect of preventing rough skin can be obtained,
The present invention has been completed.

すなわち本発明は、イブキトラノオ抽出物を含有する
ことを特徴とし、肌荒れ防止効果、肌荒れ改善効果に優
れた、皮膚の炎症を防止・緩和する皮膚外用剤を提供す
るものである。
That is, the present invention provides an external preparation for skin which is characterized by containing an extract of Ibuquitranoo and which is excellent in the effect of preventing rough skin and the effect of improving rough skin, and which prevents or reduces inflammation of the skin.

本発明において必須に使用されるイブキトラノオ抽出
物としては、イブキトラノオ(Polygonum bistorta
L.)の根茎・全草、及び一般に知られている挙参等から
抽出して得られるものであれば本発明にとって好適に使
用し得る。またこの他、イブキトラノオの同属植物であ
るムカゴトラノオ(Polygonum viviparum L.)、ハルト
ラノオ(P.tenuicaule BISS.et MOORE)等も利用でき
る。抽出方法は特に限定しないが、例えば抽出溶媒とし
て、水、メチルアルコール・エチルアルコール等の低級
一価アルコール、プロピレングリコール・1,3−ブチレ
ングリコール等の液状多価アルコール、酢酸エチルエス
テル等の低級アルキルエステル、ベンゼン・ヘキサン等
の炭化水素、エチルエーテル等が挙げられ、これらの一
種、または二種以上を組み合わせて使用し得る。これら
の抽出溶媒と共に室温又は加温して抽出し、過して得
られる抽出液、またはこれを濃縮したものが用いられ
る。
Examples of the Ibuquitranoo extract that is essential in the present invention include Ibuquitranoo (Polygonum bistorta).
L.) rhizome / whole grass, and those obtained by extracting from generally known Ginseng and the like can be preferably used in the present invention. In addition to these, it is also possible to use Mucogotranoo (Polygonum viviparum L.) and Harutoranoo (P.tenuicaule BISS.et MOORE), which are plants belonging to the same genus Ibukitoranoo. The extraction method is not particularly limited, for example, as the extraction solvent, water, a lower monohydric alcohol such as methyl alcohol and ethyl alcohol, a liquid polyhydric alcohol such as propylene glycol and 1,3-butylene glycol, a lower alkyl such as ethyl acetate. Examples thereof include esters, hydrocarbons such as benzene and hexane, ethyl ether, and the like, and these may be used alone or in combination of two or more. An extract obtained by filtering with these extraction solvents at room temperature or by heating, or a concentrate thereof is used.

皮膚外用剤中におけるイブキトラノ抽出物の含有量
は、少なすぎる場合は効果がなく、固形分として0.001
〜10.0重量%の範囲が本発明の目的の為には十分であ
り、また製品配合上からは抽出液として0.01〜20.0重量
%の範囲であれば好ましく、特に固形分として0.01〜5.
0重量%、抽出液として0.1〜10.0重量%の範囲であれば
より好ましい。
The content of Ibuquitrano extract in the external preparation for skin is ineffective if it is too small, and the solid content is 0.001.
The range of -10.0% by weight is sufficient for the purpose of the present invention, and it is preferable that it is in the range of 0.01-20.0% by weight as an extract from the viewpoint of product formulation, especially 0.01-5 as a solid content.
More preferably, it is in the range of 0% by weight and the extract as 0.1 to 10.0% by weight.

本発明において上記イブキトラノオ抽出物を配合する
皮膚外用基材としては、通常化粧品・医薬部外品・医薬
品に用いられる水性成分、粉末、界面活性剤、油分、保
湿剤、アルコール類、pH調整剤、防腐剤、酸化防止剤、
増粘剤、色素、香料等を必要に応じて適宜配合して調製
されたものであれば良い。
In the present invention, as a skin external base material containing the above-mentioned Ibuquitranoo extract, an aqueous component, a powder, a surfactant, an oil component, a moisturizer, an alcohol, a pH adjusting agent which is usually used in cosmetics / quasi drugs / pharmaceuticals. , Preservatives, antioxidants,
Any thickener, pigment, fragrance, and the like may be appropriately mixed and prepared.

本発明でいう皮膚外用剤の剤型は特に限定されず、化
粧水、乳液、クリーム、パック、軟膏、分散液等の剤型
とすることができる。
The dosage form of the external preparation for skin referred to in the present invention is not particularly limited, and may be a dosage form such as a lotion, an emulsion, a cream, a pack, an ointment, a dispersion and the like.

また、本発明の皮膚外用剤には、イブキトラノオ抽出
物の外、公知の薬剤、例えば、グリチルレチン酸及びそ
の誘導体、インドメタシン等の抗炎症剤、アスコルビン
酸、グルタチオン及びこれらの誘導体、プラセンタエキ
ス、当帰エキス、桑白皮エキス等の美白効果を有する薬
剤、紫外線吸収剤等を組み合わせて配合することも可能
であり、相乗効果を期待して製品に併用しても差し支え
ない。
In addition, the external preparation for skin of the present invention includes, in addition to the extract of Ibuquitranoo, known drugs, for example, glycyrrhetinic acid and its derivatives, anti-inflammatory agents such as indomethacin, ascorbic acid, glutathione and their derivatives, placenta extract, and the like. It is also possible to mix and combine agents having a whitening effect, such as natural extract and mulberry bark extract, and ultraviolet absorbers, and they may be used in combination with products in the hope of synergistic effect.

次に本発明に係るイブキトラノオ抽出物の抗炎症作用
を示すために次の試験を行なった。
Next, the following test was carried out in order to show the anti-inflammatory effect of the Ibuquitranoo extract according to the present invention.

(炎症抑制試験) カラゲニン足蹠浮腫法に準じ、生後5週令のウィスタ
ー系雄性ラットを1群10匹とし、起炎物質として1%カ
ラゲニン生理食塩水溶液をラット後肢足蹠に皮下注射し
て浮腫を生じさせた。
(Inflammation suppression test) According to the carrageenin footpad edema method, 10 Wistar male rats aged 5 weeks were used as a group, and 1% carrageenin physiological saline solution was used as a provocative substance by subcutaneous injection into the rat hindlimb footpad. Caused.

試料塗布群には、カラゲニン注射2時間前、1時間前
及び注射直後に、イブキトラノオ根茎メチルアルコール
抽出物を最終的に固形分として5%の割合でオリーブ油
に溶解したものを0.1mlずつ塗布し、対照群にはオリー
ブ油のみを塗布した。カラゲニン注射3時間後の浮腫容
積及び浮腫生成の抑制率を表1に示す。尚、表中の値は
各群における平均値である。
Two hours before, one hour before and immediately after the injection of carrageenin, the sample application group was prepared by applying 0.1 ml each of the methyl alcohol extract of Rhizophora rhizome finally dissolved in olive oil at a ratio of 5% as a solid content. The control group was applied only with olive oil. Table 1 shows the volume of edema and the rate of inhibition of edema formation 3 hours after the injection of carrageenin. The values in the table are average values in each group.

表1の結果から明らかな如く、本発明に係るイブキト
ラノオ抽出物は、カラゲニンにより惹起された炎症を抑
制することが認められた。
As is clear from the results in Table 1, it was confirmed that the Ibucchitrano extract according to the present invention suppressed the inflammation caused by carrageenin.

[実施例] 次に、本発明について、実施例を挙げてさらに説明す
る。これらは本発明を何ら限定するものではない。
[Examples] Next, the present invention will be further described with reference to examples. These do not limit the invention in any way.

実施例[I] クリーム (処方) (重量%) (1) イブキトラノオ全草エーテル 抽出物(固形分として) 3.0 (2) ステアリン酸 1.0 (3) ステアリルアルコール 4.0 (4) モノステアリン酸グリセリン 3.0 (5) 硬化油 7.0 (6) 流動パラフィン 10.0 (7) サフラワーオイル 2.0 (8) ソルビタンセスキオレエート 1.0 (9) 香料 0.1 (10) カルボキシビニルポリマー 0.1 (11) 水酸化ナトリウム 0.05 (12) 防腐剤 0.1 (13) 精製水 残量 (製法) A (1)〜(9)を加熱溶解する。Example [I] Cream (formulation) (% by weight) (1) Ibuquitranoo whole plant ether extract (as solid content) 3.0 (2) Stearic acid 1.0 (3) Stearyl alcohol 4.0 (4) Glycerin monostearate 3.0 ( 5) Hardened oil 7.0 (6) Liquid paraffin 10.0 (7) Safflower oil 2.0 (8) Sorbitan sesquioleate 1.0 (9) Perfume 0.1 (10) Carboxyvinyl polymer 0.1 (11) Sodium hydroxide 0.05 (12) Preservative 0.1 (13) Remaining amount of purified water (Production method) A (1) to (9) are heated and dissolved.

B (10)〜(13)を加熱溶解する。B. Dissolve (10) to (13) by heating.

C AにBを加えて乳化をし、冷却してクリームを得
る。
B is added to C A to emulsify and cool to obtain a cream.

実施例[2] 軟膏 (処方) (重量%) (1) イブキトラノオ根茎50%1,3− ブチレングリコール抽出液 1.0 (2) カルボキシビニルポリマー 1.0 (3) ヒドロキシエチルセルロース 1.0 (4) ポリエチレングリコール 10.0 (5) エチルアルコール 30.0 (6) ジイソプロピルアジペート 2.0 (7) ジイソプロパノールアミン 1.1 (8) 精製水 残 量 (製法) A (8)の一部に(2)、(3)を膨潤させる。Example [2] Ointment (formulation) (% by weight) (1) 50% ibukitranano rhizome 1,3-butylene glycol extract 1.0 (2) carboxyvinyl polymer 1.0 (3) hydroxyethyl cellulose 1.0 (4) polyethylene glycol 10.0 ( 5) Ethyl alcohol 30.0 (6) Diisopropyl adipate 2.0 (7) Diisopropanolamine 1.1 (8) Residual amount of purified water (Production method) A (8) is partially swollen with (2) and (3).

B (1)、(4)〜(6)をAに添加、撹拌する。B Add (1), (4) to (6) to A and stir.

C (8)の一部に(7)を溶解してBに添加する。C) (7) is dissolved in a part of (8) and added to B.

D Cに残量の水を加え、均一に撹拌して軟膏を得る。The remaining amount of water is added to DC and the mixture is stirred uniformly to obtain an ointment.

比較例[1] 軟膏 実施例[2]の処方中、(1)を除いて軟膏とする。Comparative Example [1] Ointment An ointment is prepared by excluding (1) in the formulation of Example [2].

上記の如くして得られた実施例[2]、比較例[2]
の軟膏を用いて、前記のカラゲニン足蹠浮腫法による炎
症抑制試験を同様にして行なった。尚、試料は各軟膏0.
1gずつ3回塗布した。結果は表2に示す。
Example [2] and Comparative Example [2] obtained as described above
In the same manner, the above-mentioned carrageenin footpad edema method was used for the inflammation suppression test using the ointment of No. The sample is 0.
1g was applied 3 times. The results are shown in Table 2.

表2の結果から明らかな如く、実施例[2]の軟膏は
皮膚の炎症を抑制する効果を有していた。また、実際に
使用したところ、実施例[2]の軟膏は、優れた肌荒れ
改善効果を有するものであった。
As is clear from the results in Table 2, the ointment of Example [2] had an effect of suppressing skin inflammation. In addition, when actually used, the ointment of Example [2] had an excellent effect of improving rough skin.

実施例[3] 化粧水 (処方) (重量%) (1) 挙参50%エチルアルコール抽出液 0.5 (2) エチルアルコール 7.0 (3) 1,3−ブチレングリコール 7.0 (4) 酢酸トコフェロール 0.05 (5) 防腐剤 0.1 (6) 香料 0.05 (7) モノオレイン酸ポリオキシ エチレンソルビタン(20E.O.) 1.0 (8) 乳酸ナトリウム 0.2 (9) セイヨウトチノキエキス 0.5 (10) 精製水 残 量 (製法) A (1)〜(7)を混合溶解する。Example [3] Lotion (prescription) (% by weight) (1) Ginseng 50% ethyl alcohol extract 0.5 (2) Ethyl alcohol 7.0 (3) 1,3-butylene glycol 7.0 (4) Tocopherol acetate 0.05 (5) ) Preservative 0.1 (6) Perfume 0.05 (7) Polyoxyethylene sorbitan monooleate (20E.O.) 1.0 (8) Sodium lactate 0.2 (9) Horse chestnut extract 0.5 (10) Residual amount of purified water (production method) A ( 1) to (7) are mixed and dissolved.

B (8)〜(10)を混合溶解する。B: Mix and dissolve (8) to (10).

C BにAを加えて混合し、化粧水を得る。A is added to CB and mixed to obtain a lotion.

[発明の効果] 以上詳述した如く、本発明は、イブキトラノオ抽出物
を必須に含有することにより、その作用効果が十分発揮
され、皮膚の炎症を防止・緩和する新規な皮膚外用剤を
提供するものである。
[Effects of the Invention] As described in detail above, the present invention provides a novel external preparation for skin, which contains the ibukitrano extract as an essential component so that its action effects are sufficiently exerted and skin inflammation is prevented and alleviated. To do.

すなわち、本発明により、抗炎症作用によって日焼け
・肌荒れ・外傷・にきび等に起因する皮膚の炎症に対し
て有効に働く、肌荒れ防止効果に優れた皮膚外用剤の提
供が可能となったのである。
That is, according to the present invention, it is possible to provide a skin external preparation having an excellent anti-roughness effect, which works effectively against inflammation of the skin caused by sunburn, rough skin, trauma, acne and the like due to its anti-inflammatory effect.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】イブキトラノオ抽出物を含有することを特
徴とする、皮膚の炎症を防止・緩和する皮膚外用剤。
1. A skin external preparation for preventing and relieving skin inflammation, which comprises an extract of Ibuquitranoo.
JP62140658A 1987-06-04 1987-06-04 Topical skin Expired - Lifetime JP2542849B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62140658A JP2542849B2 (en) 1987-06-04 1987-06-04 Topical skin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62140658A JP2542849B2 (en) 1987-06-04 1987-06-04 Topical skin

Publications (2)

Publication Number Publication Date
JPS63303909A JPS63303909A (en) 1988-12-12
JP2542849B2 true JP2542849B2 (en) 1996-10-09

Family

ID=15273759

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62140658A Expired - Lifetime JP2542849B2 (en) 1987-06-04 1987-06-04 Topical skin

Country Status (1)

Country Link
JP (1) JP2542849B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007186457A (en) * 2006-01-13 2007-07-26 Ichimaru Pharcos Co Ltd Tryptase activity inhibitor and its utilization
JP4800049B2 (en) * 2006-01-31 2011-10-26 一丸ファルコス株式会社 Formulation for activating mTOR and method for activating mTOR
FR3003758B1 (en) * 2013-03-27 2015-07-17 Basf Beauty Care Solutions France Sas COSMETIC OR DERMATOLOGICAL USE OF A POLYGONUM BISTORTA EXTRACT
JP6185743B2 (en) * 2013-04-24 2017-08-23 花王株式会社 Hair growth inhibitor

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60104005A (en) * 1983-11-08 1985-06-08 Kobayashi Kooc:Kk Skin beutifying cosmetic

Also Published As

Publication number Publication date
JPS63303909A (en) 1988-12-12

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