JPS6087224A - Emulsion-type dermatic drug for external use - Google Patents

Emulsion-type dermatic drug for external use

Info

Publication number
JPS6087224A
JPS6087224A JP58194732A JP19473283A JPS6087224A JP S6087224 A JPS6087224 A JP S6087224A JP 58194732 A JP58194732 A JP 58194732A JP 19473283 A JP19473283 A JP 19473283A JP S6087224 A JPS6087224 A JP S6087224A
Authority
JP
Japan
Prior art keywords
extract
ethanol
organic solvent
aqueous phase
drug
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
JP58194732A
Other languages
Japanese (ja)
Other versions
JPH045004B2 (en
Inventor
Makoto Fukushima
福島 信
Yoshio Kitada
北田 好男
Tadao Nakamura
中村 直生
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.)
Pola Orbis Holdings Inc
Original Assignee
Pola Chemical Industries Inc
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 Pola Chemical Industries Inc filed Critical Pola Chemical Industries Inc
Priority to JP58194732A priority Critical patent/JPS6087224A/en
Publication of JPS6087224A publication Critical patent/JPS6087224A/en
Publication of JPH045004B2 publication Critical patent/JPH045004B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • 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

Abstract

PURPOSE:To obtain the titled external drug, by extracting the crude drug such as TOKI (root of Angelica acutiloba), BYAKUSHI (root of Angelica duhurica) and SHIKON (root of Lithospermum erythrorhizon) with a specific organic solvent to obtain an oil phase containing viscous extract, esparately extracting the above crude durg with ethanol to obtain an aqueous phase containing powdery extract, and mixing and emulsifying the oily phase and the aqueous phase. CONSTITUTION:One or more crude drugs selected from TOKI, BYAKUSHI and SHIKON are extracted with an organic solvent having low polarity (e.g. benzene, n- hexane, chloroform, etc.) and the obtained viscous extract is used as a component of an oily phase. Separately, the crude drugs are extracted with a 50-80% ethanol and the obtained powdery extract is used as a component of an aqueous phase. The oily phase is mixed and emulsified with the aqueous phase to obtain the objective emulsion- type dermatic drug for external use. The ethanol fraction extract of the above three kinds of crude drugs contains a component effective to keep the moisture of the skin and give the moistness to the skin. EFFECT:Compared with the simple ethanol extraction of the crude drug, the use of the extraction residue with the organic solvent having low polarity is advantageous, and the extraction efficiency can be improved.

Description

【発明の詳細な説明】 本発明は、皮膚外用剤における薬用効果を保持しつつ、
皮膚への塗布性、吸収性を改善し、更には皮膚水分保持
機能をも付与し得る新規な乳化型皮膚外用剤に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a skin external preparation that retains its medicinal effects,
The present invention relates to a novel emulsified skin preparation for external use that has improved applicability and absorption to the skin and can also provide a skin moisture retaining function.

古米より、当帰は強壮、鎮静、通経薬として8正は鎮痛
、止血、排膿、浄血薬として、また紫根は解毒、解熱薬
として漢方の療法に広く利用さnてきた。そしてとnら
の使用にあたっては前列等の用法をもって熱水で抽出し
、その抽出液を内服するという方法が通常であった。但
し、中国では8正、当帰等を油脂で抽出し、軟膏として
使用していた事例が幾つか見うけらn。
Since ancient times, Danggui has been widely used in Chinese medicine as a tonic, sedative, and emetic, eight positives as an analgesic, hemostasis, purulent, and purifying agent, and purple root as a detoxifying and antipyretic agent. When using Ton et al., the usual method was to extract it with hot water using the method described above, and then take the extracted liquid internally. However, in China, there are several cases where 8-zheng, dang-gu, etc. were extracted with oil and fat and used as an ointment.

一方日本においても紫根と当HIIを油脂で抽出し軟膏
として使用する紫雲膏と呼ばnるものがあつ念。
On the other hand, in Japan, there is also something called shiun-yang, which is made by extracting purple root and HII with oil and using it as an ointment.

しかしこれら公知の軟膏群Fi伺nも油脂をもって抽出
する為、本発明考らの研究によって抽出成分中に11%
抗菌性、抗炎症性を有する成分は存在するものの、余効
、例えば皮膚水分保持作用、湿潤作用等を有する成分は
全く存在しないことが突止めら扛ていた。
However, since these known ointments are also extracted with fats and oils, research by the present inventors revealed that 11% of the extracted ingredients are
Although there are components that have antibacterial and anti-inflammatory properties, it has been discovered that there are no components that have aftereffects such as skin moisture retaining and moisturizing effects.

一方、前記淡方療法においても内服を中心とした適用で
あった為、その成分の外用的(特に皮膚に対して)効能
については、はとんど研究すらさnていないのが実情で
あった。
On the other hand, since the above-mentioned euphonic therapy was mainly applied internally, the reality is that there has been little research into the effectiveness of its ingredients externally (especially on the skin). Ta.

そこで本発明者らは、この皮屑に対する前記3種の生薬
の効能を詳細に調べたところ、抽出溶媒として50−8
0%エタノールを用いた分画抽出物中に、皮膚の水分を
保持し、潤いを与える成分が存在すると(を見出した。
Therefore, the present inventors investigated in detail the efficacy of the above-mentioned three types of crude drugs against this skin debris, and found that 50-8
It was discovered that components that retain moisture and moisturize the skin are present in a fractionated extract using 0% ethanol.

更に、皮膚外用剤としての効能をより発揮させる為、前
記3種の生薬を水と相溶性のほとんどない有機溶媒で抽
出し、その成分上油相中に、また上記50〜80%エタ
ノール分画抽出物を水相中にそれぞn含有させ、こnら
ti合乳化することKより優n穴皮屑外用剤が得らnる
ことを知シ本発明を完成させたものである。
Furthermore, in order to further demonstrate the efficacy as an external skin preparation, the three herbal medicines mentioned above were extracted with an organic solvent that has little compatibility with water, and the above 50-80% ethanol fraction was extracted into the oil phase. The present invention has been completed by the knowledge that a topical preparation for skin dregs can be obtained by incorporating the extracts into the aqueous phase and emulsifying them.

本発明は当帰、8正、紫根よシ選択さnる1種または2
種以上の生薬を極性の低い有機溶媒で抽出処理して得ら
nた粘稠状エキスを含有する油相と、該生薬を50〜8
0%エタノールで抽出処理して得らnた粉末状抽出物を
含有する水相とを、a合乳化してなる乳化型皮屑外用剤
に関するものである。
The present invention is based on one or two selected types of present invention, eight positive, and purple roots.
An oil phase containing a viscous extract obtained by extracting different types of herbal medicines with a low polarity organic solvent, and
The present invention relates to an emulsified skin shavings external preparation prepared by emulsifying an aqueous phase containing a powdered extract obtained by extraction with 0% ethanol.

本発明において油相中に含有さnる粘稠状エキスは次の
ような方法で調整さnる。すなわち先ず当帰、8正、紫
根の5種の生薬から目的に応じて任意K11g1乃至は
2a以上を選択し、こnt水と相溶性のほとんどない例
えばベンゼン。
In the present invention, the viscous extract contained in the oil phase is prepared by the following method. That is, first, any K11g1 to 2a or more is selected depending on the purpose from five types of herbal medicines: Dangki, 8-sei, and Shikon, and this is used, for example, benzene, which has almost no compatibility with water.

n−ヘキサン、クロロホルム、エーテル等)極性の低い
有機溶媒の単独もしくは混合溶媒中で温浸抽出処理し、
口過したロ液′t−適宜な方法により濃縮乾固して得ら
nる。こn′t−通常の乳化の際油相として用いるエー
テル類、エステル類、炭化水素類に溶解し、とnt−乳
化物の油相として用いる。
Digestion extraction treatment in a single or mixed solvent of a low polar organic solvent (n-hexane, chloroform, ether, etc.),
The filtered filtrate is obtained by concentrating to dryness by an appropriate method. It is dissolved in ethers, esters, and hydrocarbons used as the oil phase during normal emulsification, and used as the oil phase of the nt-emulsion.

また、水相中に含有さnる粉末状抽出物の調整法は以下
の通りである。前記3橡の生薬を50〜80%エタノー
ルで常温下または温浸抽出処理し、口過した口液を濃縮
すると皮膚の水分を保ち潤いを与える成分を含んだもの
が得らnる。しかし%仕済的(コスト的)観点から見た
時には、生薬からjILfiに50〜8ONエタノール
抽出するよシも、前記極性の低い有機溶媒による抽出し
た後の抽出!l!E1!r、用いることがより有利であ
シ、t7を抽出効率をよシ高める為には次のような別法
に従かうのがより冥際的である。即ち、主薬を極性の低
い有機fI!媒で抽出処理し、口過後1残fIiを水ま
たに熱水で充分に再抽出する。その後口遇し、cl液を
操作上便利な程度までam+する。次いでこれにアルコ
ールシタえ、そのアルコール濃度が50〜80%になる
ようにkJ11整する。すると不浴物(このものには水
分保持能がほとんどない)が沈殿してくるのでとn1口
適し、a液を集め濃縮乾固すると上述と同じ成分を含有
したものf、1得らnる。
Further, the method for preparing the powdered extract contained in the aqueous phase is as follows. When the three herbal medicines are extracted with 50-80% ethanol at room temperature or by digestion, and the oral fluid is concentrated, a product containing ingredients that retain moisture and moisturize the skin can be obtained. However, from a cost perspective, it is better to extract jILfi from herbal medicines with 50 to 8ON ethanol, but it is better to extract the jILfi after extraction with the organic solvent with low polarity. l! E1! It is more advantageous to use t7, and in order to further improve the extraction efficiency of t7, it is more practical to follow the following alternative method. That is, the main drug is a low polar organic fI! After filtration, the remaining fIi is sufficiently re-extracted with water or hot water. Thereafter, the Cl solution is am+ed to an extent convenient for operation. Next, add alcohol to this and adjust kJ11 so that the alcohol concentration is 50 to 80%. Then, unbathable substances (this substance has almost no water retention ability) will precipitate, so when liquid a is collected and concentrated to dryness, a liquid containing the same components as above is obtained. .

以上の様にして得らnた抽出物の水分保持機能を評価す
る為、本発明者らは人の足よシ剥離した角l−を用い下
記の1)%2)の方法によシその効果を検足した。その
結果については表−1及−^ − び2に示す。
In order to evaluate the water retention function of the extract obtained as described above, the present inventors used exfoliated horns of human feet and performed the following methods 1) and 2). I checked the effect. The results are shown in Tables 1, 2 and 2.

1)抽出物を用いた沖j定 0試料二A、水可溶、75%KtOH不溶部分(沈殿物
) B、水及び75%EtOH可溶部分 O0尿累(対f!@) p、水(コントロール) C方法:厚さ0.5 amm s直径1αの錠剤にプレ
スした角5t−1上記A%B%Cの5%水浴液及びD中
に50分間l!!潰し、次いで余分な液をティッシュA
 +++ A−で験く拭きを9.こnを20℃、 93%の一定温湿度下に放置し、5 日後の角層I D 011g当シの水分残存(保持):
Jtt測定した。n−5゜ 2)抽出物を含有するクリームを用いた測定#に科:a
、n−ヘキサン抽出エキス’(H2wt%含有したクリ
ーム b、水可溶、75%EtOE不溶部分 (沈殿物)を5wt%含有したク  6− リーム C0水及び75チEtOH可溶部分を5wt*含有した
クリーム (1,a及びCの両成分を含有(7wtチ)したクリー
ム(本発明品) O方法:1)の方法と同様にして行なった。n=5゜ 表−1水分保持量(抽出物)(n=5平均値)表−2水
分保持f(クリーム)(n=5平均値)表−1,2の結
果が示すように、白正、当帰、紫根の水及び751Et
OI(可溶抽出部分には明白な皮膚水分保持効果がある
ことがわかる。また表−2のクリームd(本発明品)に
おいても、水分保持効果のいささかの減少も見らnず、
漢方軟膏が持っている予想さnる作用を加味し優nた皮
膚外用剤を提供できるようになる。尚。
1) Sample 2 using extract A, water soluble, 75% KtOH insoluble part (precipitate) B, water and 75% EtOH soluble part O0 urine cumulative (vs.f!@) p, water (Control) Method C: A corner 5t-1 pressed into a tablet with a thickness of 0.5 amm s and a diameter of 1α was placed in a 5% water bath solution of the above A%B%C and D for 50 minutes! ! Crush it, then drain the excess liquid with tissue A.
+++ Try wiping with A-9. This was left at a constant temperature and humidity of 20°C and 93%, and after 5 days, the moisture remaining (retention) in the stratum corneum ID 011g:
Jtt was measured. n-5゜2) Measurement using cream containing extract #: a
, n-hexane extracted extract' (cream b containing 2 wt% of H, water soluble, cream containing 5 wt% of 75% EtOE insoluble portion (precipitate) 6-cream C0 containing 5 wt% of water and 75% EtOH soluble portion* Cream containing both components (1, A and C (7wt) (product of the present invention) Method O: The same method as in 1) was conducted.n=5゜Table-1 Moisture Retention (Extracted) (n = 5 average value) Table 2 Moisture retention f (cream) (n = 5 average value) As the results in Tables 1 and 2 show, Hakusei, Toki, Shikon water and 751Et
It can be seen that the OI (soluble extracted part) has a clear skin moisture retention effect. Also, in Cream d (product of the present invention) in Table 2, no decrease in the moisture retention effect was observed.
It becomes possible to provide an excellent external preparation for the skin by taking into account the expected effects of Chinese herbal ointments. still.

念のため市販の紫雲膏と本発明のクリームdとの創傷治
癒効果(治癒軍、治癒日数)の比較検討をウサギを用い
て測定したところ紫雲膏と同等乃至はそn以上の効果が
見らnた。
Just to be sure, we compared the wound healing effects (healing forces, healing days) of commercially available Shiun Gypsum and Cream d of the present invention using rabbits, and found that it had an effect equal to or better than that of Shiun Gypsum. It was.

本発明により得られる乳化型皮膚外用剤は、更に以下に
挙げる如き利点及び特徴を肩するものである。
The emulsified skin preparation obtained by the present invention further has the following advantages and characteristics.

(1)今までの漢方軟膏は硬く適量をとりすらく、皮膚
の表面に均一に塗布しに< 25為ったが乳化すること
によりこの欠点は解消さn友。
(1) Conventional Chinese herbal ointments are hard and difficult to apply in an appropriate amount, making it difficult to apply them evenly to the skin surface, but emulsification eliminates this drawback.

(21漢方の軟ifは油脂で4温で抽出することによシ
油脂の酸化が促進さ几皮膚に悪い作用を及ぼすpov他
の上昇が見ら几たが今回こnが解消さnた。
(21 Chinese medicine soft if extracts with oil at 4 temperatures promotes the oxidation of the oil and fat, but an increase in POV and other factors that have a negative effect on the skin was observed, but this problem has been resolved this time.

(3)乳化することにより、薬効成分の吸収がよくない
1桑の使用tt軟質の時より減ら丁ことが出来るように
なった。
(3) By emulsifying, it is possible to use less mulberry than in the case of soft mulberry, which does not absorb the medicinal ingredients well.

 9− 以下に本発明の冥施例を示す。尚、処方中の配合割合は
そn −t” n重量部である。
9- Examples of the present invention are shown below. The blending ratio in the prescription is n-t''n parts by weight.

実施例1 クリーム 当帰100 t s8正100fを混合し、ヘキサン1
tで2回温浸し、口過し7’Cロ液を濃縮乾固しこay
エキス1とする。次に口過した残渣を熱水1.5tで2
回抽出し、口遇したΩ液を適当に濃縮し、アルコールシ
タえてそのts度が80%となるように調製する。次に
沈殿したものを口遇し、0液を濃縮乾固し、エキス2と
する。
Example 1 Mix 100 t of cream and 100 f of s8, and add 1 part of hexane.
Digest twice at t and concentrate the 7'C filtrate to dryness.
Let it be extract 1. Next, the filtered residue was washed with 1.5 tons of hot water for 2 hours.
Extract twice, concentrate the obtained Ω solution appropriately, and add alcohol to adjust the TS content to 80%. Next, the precipitate is mixed, and the 0 liquid is concentrated to dryness to obtain Extract 2.

こnらエキス1%エキス2を次に示すクリーム処方中に
そn−tJn配合し乳化する。
These extracts 1% extract 2 were blended into the following cream formulation and emulsified.

!l!施例2 乳液 当帰、8正、紫根を709ずつ増り混合する。! l! Example 2 Emulsion Increase Toki, 8 Sei, and Shikon by 709 and mix.

混合物をエーテル1tで2回温浸し、口過しQ液を濃縮
乾固し、エキス1とする。次に残at−熱水1.5tで
2回抽出し、Q液を適当に濃縮し、アルコールを加え、
その濃度が70%となるように調製する。こnt−口過
し、0液を濃縮乾固し、エキス2とする。こnらエキス
1、及び2を下に示す乳液処方中にそ1ぞれ配付し乳化
する。
The mixture was digested twice with 1 t of ether, and the filtered Q solution was concentrated to dryness to obtain Extract 1. Next, extract the remaining attenuate twice with 1.5 t of hot water, concentrate the Q solution appropriately, add alcohol,
Adjust the concentration to 70%. This was passed through the mouth, and the 0 solution was concentrated to dryness to obtain Extract 2. Each of these extracts 1 and 2 was distributed into the emulsion formulation shown below and emulsified.

Claims (1)

【特許請求の範囲】 1)@帰、8正、紫根よυ選択さnる1棟または2種以
上の生薬を極性の低い有機溶媒で抽出処理して得らnた
粘稠状エキスt−含有する油相と一該生薬を50〜80
Xエタノールで抽出処理して得らf′した粉末状抽出物
を含有する水相とヲ、混合乳化してなる乳化型皮膚外用
剤。 2)極性の低い有機溶媒がベンゼン、n−ヘキサン、ク
ロロホルム、エーテル等よ#)a択さnる18!または
2棟以上の混合物である特許請求の範囲第1)項記載の
乳化型皮膚外用剤。 3)粉末状抽dI!!IJがg:桑を極性の低い有機溶
媒で抽出処理して得らnた抽出残渣を50〜80%エタ
ノールで再抽出処理して得らnたものである特許請求の
範囲第1)項記載の乳化型皮膚外用剤。
[Scope of Claims] 1) A viscous extract obtained by extracting one or more selected herbal medicines, such as @ki, 8sei, and purple root, with a low polarity organic solvent. The oil phase and the herbal medicine containing 50 to 80%
An emulsified skin preparation prepared by mixing and emulsifying an aqueous phase containing a powdered extract obtained by extraction with X ethanol. 2) Select a less polar organic solvent such as benzene, n-hexane, chloroform, ether, etc. or the emulsified skin preparation for external use according to claim 1, which is a mixture of two or more. 3) Powdered extraction dI! ! IJ is obtained by re-extracting the extraction residue obtained by extracting mulberry with a low polar organic solvent with 50 to 80% ethanol, as described in claim 1). emulsified skin preparation for external use.
JP58194732A 1983-10-18 1983-10-18 Emulsion-type dermatic drug for external use Granted JPS6087224A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58194732A JPS6087224A (en) 1983-10-18 1983-10-18 Emulsion-type dermatic drug for external use

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58194732A JPS6087224A (en) 1983-10-18 1983-10-18 Emulsion-type dermatic drug for external use

Publications (2)

Publication Number Publication Date
JPS6087224A true JPS6087224A (en) 1985-05-16
JPH045004B2 JPH045004B2 (en) 1992-01-30

Family

ID=16329309

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58194732A Granted JPS6087224A (en) 1983-10-18 1983-10-18 Emulsion-type dermatic drug for external use

Country Status (1)

Country Link
JP (1) JPS6087224A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60199807A (en) * 1984-03-22 1985-10-09 Kao Corp Humectant
JPS60258104A (en) * 1984-06-06 1985-12-20 Inahata Koryo Kk Cosmetic composition having moisture retention
JPWO2003086433A1 (en) * 2002-04-15 2005-08-18 哲夫 山東 Dermatitis treatment cream
JPWO2003086432A1 (en) * 2002-04-15 2005-08-18 哲夫 山東 Dermatitis lotion
CN102697857A (en) * 2012-05-29 2012-10-03 株洲千金药业股份有限公司 Maternal towel liquid medicament for preventing puerperal infection and preparation method thereof
JP2014527989A (en) * 2011-09-30 2014-10-23 伽藍(集団)股▲分▼有限公司 Microemulsion containing button extract and its preparation method and application
CN112156128A (en) * 2020-11-11 2021-01-01 苏州健雄职业技术学院 Preparation method of multi-effect lithospermum paste for infants

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60199807A (en) * 1984-03-22 1985-10-09 Kao Corp Humectant
JPS60258104A (en) * 1984-06-06 1985-12-20 Inahata Koryo Kk Cosmetic composition having moisture retention
JPH0140002B2 (en) * 1984-06-06 1989-08-24 Inahata Koryo Kk
JPWO2003086433A1 (en) * 2002-04-15 2005-08-18 哲夫 山東 Dermatitis treatment cream
JPWO2003086432A1 (en) * 2002-04-15 2005-08-18 哲夫 山東 Dermatitis lotion
US7572469B2 (en) 2002-04-15 2009-08-11 Tetsuo Santo Therapeutic lotion for dermatitis
JP2014527989A (en) * 2011-09-30 2014-10-23 伽藍(集団)股▲分▼有限公司 Microemulsion containing button extract and its preparation method and application
CN102697857A (en) * 2012-05-29 2012-10-03 株洲千金药业股份有限公司 Maternal towel liquid medicament for preventing puerperal infection and preparation method thereof
CN112156128A (en) * 2020-11-11 2021-01-01 苏州健雄职业技术学院 Preparation method of multi-effect lithospermum paste for infants
CN112156128B (en) * 2020-11-11 2022-07-22 苏州健雄职业技术学院 Preparation method of multi-effect lithospermum paste for infants

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