JPH0138762B2 - - Google Patents
Info
- Publication number
- JPH0138762B2 JPH0138762B2 JP59235423A JP23542384A JPH0138762B2 JP H0138762 B2 JPH0138762 B2 JP H0138762B2 JP 59235423 A JP59235423 A JP 59235423A JP 23542384 A JP23542384 A JP 23542384A JP H0138762 B2 JPH0138762 B2 JP H0138762B2
- Authority
- JP
- Japan
- Prior art keywords
- ginseng
- polysaccharide
- panax
- medicinal
- cosmetic
- 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics 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
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Botany (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
Description
この発明は薬用ニンジン中に存在する多糖類を
有効成分として配合した、皮膚及び毛髪の美容と
健康に好適な化粧料に関する。
薬用ニンジン中、特にウコギ科(Araliaceae)
に属するオタネニンジン(パナツクス・ギンセン
グ、シー・エー・メイヤー、Panax dinseng C.
A.MEYER)は一名チヨウセンニンジンと呼ば
れ、古来より強壮、強精、消炎、利尿、血圧降
下、抗糖尿用の薬剤として用いられてきたことは
広く知られるところである。近時、これらの薬効
が、チヨウセンニンジン中のサポニン成分による
のではないかとの研究が進められている。
この発明の発明者らは、薬用ニンジンに、サポ
ニン成分ではなくて従来その存在が知られていな
かつた多糖類が含有され、しかもこの多糖類が皮
膚賦活作用を有することを見出してこの発明に到
達したものである。
得られた多糖類の特性は、原料の薬用ニンジン
の種類によつて若干異なるがいずれも下記のよう
な特性を有する。
(i) 皮膚賦活作用を有する
(ii) 水に可溶、メタノールに難溶、エタノール、
エーテル、ベンゼン、クロロホルム及びアセト
ンに不溶
(iii) 1%水溶液のPHは約5.5
(iv) 分解温度
約218℃
(v) 2%フエノール水溶液と濃硫酸との混液で淡
黄赤色を呈しかつ銀鏡反応とフエーリング試液
に陽性
かくしてこの発明は、薬用ニンジンに含有さ
れ、上記特性を有することによつて特徴づけられ
る多糖類を有効成分として含有することを特徴と
する化粧料を提供するものである。
この発明における多糖類を含有するニンジンと
しては、オタネニンジンが最も好ましいものであ
る。その他、これと類緑植物であるトチバニンジ
ン(パナツクス・ヤポニクス、シー・エー・メイ
ヤー、Panax japonicus C.A.MEYER)、アメリ
カニンジン(パナツクス・キンキエホリウム、リ
ンネ、Panax quinquefolium LINNE)、三七ニ
ンジン(パナツクス・ノトギンセング・バーギ
ル、Panax notoginseng BURKILLまたはパナ
ツクス・プソイドギンセング、ワーリツヒPanax
pseudoginseng WALLICH)が挙げられる。
この発明の多糖類の原料としては、上記ニンジ
ンの根及び根茎のなま、乾燥品及び生薬、並びに
上記ニンジンを組織培養して得た培養組織を用い
ることができる。そして、有効成分の多糖類は次
のようにして得られる。
まず上記原料を脱脂しないままか又は通常の脂
溶性溶媒を用いて脱脂後、水又は水性有機溶媒で
抽出される(原料の5〜7倍相当量)。抽出は水
で十分行えるが、抽出液の腐敗を防止するために
水性有機溶媒を用いてもよく、また両方で抽出し
てもよい。水性有機溶媒の有機溶媒としてはメタ
ノール、エタノールなどの低級アルコール又はア
セトンが用いられ、原料の種類などによつて50%
以下、好ましくは30%以下の有機溶媒含有のもの
が用いられる。またこの抽出は加温することによ
つて促進され、原料は破砕もしくは粉砕するのが
好ましい。
得られた抽出液そのまま、これを減圧下濃縮し
た濃縮液、又は該抽出液や濃縮液に低級アルコー
ルを添加して目的物質を沈澱させこれを濾別しエ
タノールで洗滌して得た沈澱物を、水に溶解した
溶液をそれぞれ内液として、24オングストローム
以下の大きさの物質を除去するセルロース透析膜
〔ビスキング社製の36/32型〕によつて、水を外
液として用い6日間にわたつて透析する。また上
記抽出液を減圧下乾燥して得たエキスを水に溶解
し不溶物を除去した溶液を透析に付してもよい。
上記のようにして得られた透析内液を減圧下乾
燥して淡褐白色のこの発明の多糖類の粉末が得ら
れる。
次にこの発明の多糖類の製造例を述べる。
薬用ニンジン多糖類の製造例 1
オタネニンジン(4年生)の乾燥根10Kgを細切
し、約60の水:メタノール(1:1)混合液に
撹拌しながら3日間室温で浸漬して抽出する。こ
の抽出を合計2回行つた後、さらに残渣を約60
の水に撹拌しながら3日間浸漬して抽出する。全
抽出液を合して濾過し、減圧下溶媒を留去して約
10まで濃縮する(発泡する場合n−ブタノール
を少量加えて消泡する)。得られた濃縮液を濾過
して不溶物を除去する。この濾液をビスキング社
製の36/32型セルロース透析膜中に入れ、精製水
を外液として6日間透析を行う。得られた内液を
60℃以下で減圧下溶媒を留去し、デシケータ中で
一夜乾燥して淡褐白色粉末の多糖類152gを得た。
この生成物は下記の物性を有する多糖類であり、
後記のような皮膚賦活作用を有する。
(i) 淡褐白色〜白色の粉末で無味無臭ある。
(ii) 水に可溶であり、メタノールに難溶、エタノ
ール、エーテル、ベンゼン、クロロホルム及び
アトンに不溶
(iii) 1%水溶液のPHは約5.5である。
(iv) 赤外吸収スペクトル(KBr法)
νmax:3450、1745、1625、1415、1350、1250
及び1020cm-1
(v) 核磁気共鳴スペクトル(90MHz、D2O)
5.21(s)、3.63(s)、3.56(s)、3.49(s)、
3.43(s)及び3.34(s)
(vi) 分解温度
約218℃
(vii) 比旋光度
〔α〕25 D+116゜(c5、水)
(viii) 呈色、沈澱反応
a 1%水溶液1mlに2%フエノール水溶液1
mlを濃硫酸1mlを加えると淡黄色を呈する。
b 1%水溶液2〜3滴を沸騰フエーリング試
薬5mlに加えると赤色沈澱を生ずる。
c 1%水溶液は銀鏡反応に対し陽性である。
(ix) 元素分析
元素、水素、酸素及び窒素の核原子が含まれ
ている。
薬用ニンジン多糖類の製造例 2
オタネニンジン(4年生)の乾燥根10Kgを細切
し、約60の水に撹拌しながら3日間室温で浸漬
して抽出する。この抽出を合計3回行つた後、全
抽出液を合して濾過する。この濾液を減圧下溶媒
を留去して約10まで濃縮する(発泡する場合n
ブタノールを少量加えて消泡する)。得られた濃
縮液に約100のエタノールを加えて粗多糖類を
析出させて濾別し3のエタノールで洗浄し減圧
下溶媒を除去して淡褐色白色粉末の粗多糖類を約
350gを得た。この多糖類を10の精製水に溶解
し濾過して不溶物を除去する。この濾液をビスキ
ング社製の36/32型セルロース透析膜中に入れ精
製水を外液として6日間透析を行う。得られた内
液を約100のエタノール中に注加し析出する絮
状沈澱を濾取し60℃以下で減圧下溶媒を留去し、
デシケータ中で一夜乾燥して淡褐白色粉末の多糖
類210gを得た。この生成物は製造例1の多糖類
と同様の物性と皮膚賦活作用を有する。
この発明の化粧料の剤形は化粧水、ローシヨ
ン、クリーム、パツクなどの皮膚化粧料、シヤン
プー、ヘヤトニツク、トリートメント、ヘヤクリ
ームなどの毛髪化粧料、シロツプ、茶、錠剤など
の内服美容化粧料又は石けんなどのいずれであつ
てもよい。
この発明の化粧料に用いる化粧用に受容な基剤
としては当該技術分野で公知のものを使用するこ
とができる。
またこの発明の化粧料には、香料、酸化防止
剤、防腐剤、界面活性剤などの各種添加剤を、必
要に応じて適宜加えてもよい。
またこの発明の化粧料は当該技術分野の調製法
によつて製造することができる。
そしてこの発明の化粧料には、一般に前記の多
糖類が0.001〜3重量%添加され、適切なものは
0.01〜0.5重量%、より好ましくは0.01〜0.1重量
%添加される。
化粧料が特に石けんの場合には前記多糖類は
0.01〜0.5重量%添加するのが好ましい。
次にこの発明の薬用ニンジン多糖類を有効成分
として含有する各種化粧料の実施例を示す。いず
れも処方のみを記載したがこれらの処方の化粧料
は常法によつて製造できる。
実施例 1
(化粧水)
エチルアルコール 15.00%
薬用ニンジン粘液多糖類 0.10
グリセリン 8.00
プロピレングリコール 5.00
ポリオキシエチレンオレイン 2.00
アルコールエーテル
香 料 0.50
精製水 69.40
実施例 2
(クリーム)
薬用ニンジン粘液多糖類 0.10%
ステアリン酸 8.00
プロピレングリコール 5.00
オリーブ油 5.00
ポリオキシエチレンソルビタン 3.00
モノステアレート
イソプロピルミリステート 2.00
香 料 0.30
精製水 76.60
実施例 3
(ヘヤトニツク)
薬用ニンジン粘液多糖類 0.05%
エチルアルコール 55.00
グリセリン 5.00
ポリオキシエチレンオレイル 2.00
アルコールエーテル
香 料 0.25
精製水 37.70
実施例 4
(ミルクローシヨン)
薬用ニンジン粘液多糖類 0.05%
ステアリン酸 10.00
セチルアルコール 8.00
グリセリンモノステアレート 8.00
ラノリン 2.00
ポリオキシエチレンソルビタン 0.20
モノステアレート
香 料 0.30
精製水 71.45
実施例 5
(透明石けん)
薬用ニンジン粘液多糖類 0.20%
石けん分 60.00
蔗 糖 11.50
グリセリン 9.40
エチルアルコール 0.90
香 料 1.40
染料その他 1.10
精製水 15.50
次にこの発明の化粧料の使用効果について説明
する。
(i) 試験方法
30〜40才の女性で肌あれのひどい人、しみの
ある人、かゆみの強い人をそれぞれ20名づつ試
験対象として選んだ。
実施例2の処方のクリームを、上記の肌あれ
としみのグループに朝夕2回2ケ月間、かゆみ
のグループには朝夕2回1ケ月間、それぞれ連
続塗布し、さらに実施例5の処方の透明石けん
を肌あれグループとしみグループに1日1回入
浴時に2ケ月使用して、その効果を次の方法で
調べた。
すなわち各症状について下記第1表に示す5
段階の評価基準を作成し、前記使用試験の前後
の症状を第1表に段階で判定した。
This invention relates to cosmetics suitable for the beauty and health of skin and hair, containing polysaccharides present in medicinal ginseng as active ingredients. Medicinal ginseng, especially Araliaceae
Panax ginseng (Panax ginseng, C.A. Meyer, Panax ginseng C.
A. MEYER), also known as Panax ginseng, is widely known to have been used as a tonic, tonic, anti-inflammatory, diuretic, blood pressure lowering, and anti-diabetic drug since ancient times. Recently, research has been underway to investigate whether these medicinal effects may be due to the saponin components in Panax ginseng. The inventors of this invention arrived at this invention by discovering that medicinal ginseng contains not a saponin component but a polysaccharide whose existence was previously unknown, and that this polysaccharide has a skin revitalizing effect. This is what I did. The properties of the obtained polysaccharide vary slightly depending on the type of medicinal ginseng used as the raw material, but all have the following properties. (i) Has a skin activating effect (ii) Soluble in water, sparingly soluble in methanol, ethanol,
Insoluble in ether, benzene, chloroform and acetone (iii) PH of 1% aqueous solution is approximately 5.5 (iv) Decomposition temperature approximately 218℃ (v) A mixture of 2% phenol aqueous solution and concentrated sulfuric acid exhibits a pale yellow-red color and a silver mirror reaction. Thus, the present invention provides a cosmetic material containing as an active ingredient a polysaccharide contained in medicinal ginseng and characterized by having the above-mentioned properties. Panax ginseng is the most preferred carrot containing polysaccharide in this invention. In addition, there are other green plants such as Panax ginseng (Panax japonicus CAMEYER), American ginseng (Panax quinquefolium LINNE), Panax ginseng (Panax quinquefolium LINNE), Panax notoginseng BURKILL or Panax pseudoginseng, Panax
pseudoginseng WALLICH). As raw materials for the polysaccharide of the present invention, raw, dried, and herbal medicines of the roots and rhizomes of the carrot, and cultured tissue obtained by tissue culturing the carrot can be used. The active ingredient polysaccharide can be obtained as follows. First, the raw material is extracted with water or an aqueous organic solvent (equivalent to 5 to 7 times the amount of the raw material), either undefatted or after defatted using a normal fat-soluble solvent. Although water is sufficient for extraction, an aqueous organic solvent may be used to prevent spoilage of the extract, or extraction may be performed with both. As the organic solvent for the aqueous organic solvent, lower alcohols such as methanol and ethanol, or acetone are used, and depending on the type of raw materials, 50%
Hereinafter, those containing an organic solvent of 30% or less are preferably used. Further, this extraction is promoted by heating, and the raw material is preferably crushed or pulverized. The obtained extract as it is, a concentrated liquid obtained by concentrating this under reduced pressure, or a lower alcohol is added to the extracted liquid or concentrated liquid to precipitate the target substance, which is filtered and washed with ethanol to obtain a precipitate. , using a solution dissolved in water as the inner solution and using a cellulose dialysis membrane (model 36/32 manufactured by Visking) that removes substances with a size of 24 angstroms or less for 6 days using water as the outer solution. and undergo dialysis. Alternatively, the extract obtained by drying the above extract under reduced pressure may be dissolved in water, and the solution obtained by removing insoluble matter may be subjected to dialysis. The dialysis solution obtained as described above is dried under reduced pressure to obtain a light brown-white powder of the polysaccharide of the present invention. Next, an example of producing the polysaccharide of this invention will be described. Example of producing medicinal carrot polysaccharide 1 Cut 10 kg of dried roots of Panax ginseng (4th year old) into small pieces, and extract by immersing them in a mixture of water and methanol (1:1) for 3 days with stirring at room temperature. After performing this extraction twice in total, approximately 60% of the residue
Extract by soaking in water for 3 days while stirring. All the extracts were combined and filtered, and the solvent was distilled off under reduced pressure to give a volume of approx.
Concentrate to 10% (if foaming occurs, add a small amount of n-butanol to defoam it). The obtained concentrate is filtered to remove insoluble matter. This filtrate is placed in a 36/32 type cellulose dialysis membrane manufactured by Visking, and dialysis is performed for 6 days using purified water as an external liquid. The obtained internal fluid
The solvent was distilled off under reduced pressure at 60° C. or lower, and the residue was dried overnight in a desiccator to obtain 152 g of a pale brown-white powder of polysaccharide.
This product is a polysaccharide with the following physical properties,
It has skin revitalizing effects as described below. (i) It is a pale brown to white powder, tasteless and odorless. (ii) Soluble in water, sparingly soluble in methanol, insoluble in ethanol, ether, benzene, chloroform and atone (iii) PH of 1% aqueous solution is approximately 5.5. (iv) Infrared absorption spectrum (KBr method) νmax: 3450, 1745, 1625, 1415, 1350, 1250
and 1020cm -1 (v) nuclear magnetic resonance spectrum (90MHz, D 2 O) 5.21 (s), 3.63 (s), 3.56 (s), 3.49 (s),
3.43 (s) and 3.34 (s) (vi) Decomposition temperature: Approximately 218℃ (vii) Specific rotation [α] 25 D + 116゜ (c5, water) (viii) Coloration, precipitation reaction a 2 in 1 ml of 1% aqueous solution % phenol aqueous solution 1
When 1 ml of concentrated sulfuric acid is added to the solution, it becomes pale yellow. b Adding 2-3 drops of a 1% aqueous solution to 5 ml of boiling Fehling's reagent produces a red precipitate. c 1% aqueous solution is positive for silver mirror reaction. (ix) Elemental analysis Contains nuclear atoms of the elements, hydrogen, oxygen and nitrogen. Production example of medicinal carrot polysaccharide 2 Cut 10 kg of dried roots of Panax ginseng (fourth year old) into small pieces, and extract by immersing them in about 60 ml of water at room temperature for 3 days with stirring. After performing this extraction three times in total, all extracts are combined and filtered. The filtrate is concentrated to about 10% by distilling off the solvent under reduced pressure (in case of foaming, n
Add a small amount of butanol to defoam). Approximately 100 ml of ethanol was added to the obtained concentrate to precipitate the crude polysaccharide, which was filtered and washed with ethanol from step 3. The solvent was removed under reduced pressure to obtain the crude polysaccharide as a light brown white powder.
Obtained 350g. This polysaccharide is dissolved in 10 purified water and filtered to remove insoluble matter. This filtrate is placed in a 36/32 type cellulose dialysis membrane manufactured by Visking and dialyzed for 6 days using purified water as an external liquid. The obtained internal solution was poured into about 100 ml of ethanol, the precipitate was collected by filtration, and the solvent was distilled off under reduced pressure at a temperature below 60°C.
The mixture was dried in a desiccator overnight to obtain 210 g of a pale brownish white powder polysaccharide. This product has the same physical properties and skin revitalizing effect as the polysaccharide of Production Example 1. The dosage forms of the cosmetics of this invention include skin cosmetics such as lotions, lotions, creams, and packs, hair cosmetics such as shampoos, hair tonics, treatments, and hair creams, oral beauty cosmetics such as syrups, teas, tablets, and soaps. It may be any of the following. As the cosmetically acceptable base used in the cosmetic composition of the present invention, those known in the art can be used. Furthermore, various additives such as fragrances, antioxidants, preservatives, and surfactants may be added to the cosmetics of the present invention as appropriate. Further, the cosmetic composition of the present invention can be manufactured by a preparation method known in the art. The cosmetics of this invention generally contain 0.001 to 3% by weight of the above-mentioned polysaccharides, and suitable ones include
It is added in an amount of 0.01 to 0.5% by weight, more preferably 0.01 to 0.1% by weight. When the cosmetic is especially soap, the polysaccharide is
It is preferable to add 0.01 to 0.5% by weight. Next, examples of various cosmetics containing the medicated ginseng polysaccharide of the present invention as an active ingredient will be shown. In each case, only the prescriptions are described, but cosmetics with these formulations can be manufactured by conventional methods. Example 1 (Lotion) Ethyl alcohol 15.00% Medicated carrot mucilage polysaccharide 0.10 Glycerin 8.00 Propylene glycol 5.00 Polyoxyethylene olein 2.00 Alcohol ether fragrance 0.50 Purified water 69.40 Example 2 (Cream) Medicinal carrot mucilage polysaccharide 0.10% Stearic acid 8.00 Propylene glycol 5.00 Olive oil 5.00 Polyoxyethylene sorbitan 3.00 Isopropyl myristate monostearate 2.00 Fragrance 0.30 Purified water 76.60 Example 3 (Heatnik) Medicinal carrot mucilage polysaccharide 0.05% Ethyl alcohol 55.00 Glycerin 5.00 Polyoxyethylene oleyl 2. 00 Alcohol ether scent Material 0.25 Purified water 37.70 Example 4 (Milk lotion) Medicinal carrot mucilage polysaccharide 0.05% Stearic acid 10.00 Cetyl alcohol 8.00 Glycerin monostearate 8.00 Lanolin 2.00 Polyoxyethylene sorbitan 0.20 Monostearate flavor 0.30 Purified water 71.45 Example 5 (Transparent soap) Medicinal carrot mucilage polysaccharide 0.20% Soap content 60.00 Sucrose 11.50 Glycerin 9.40 Ethyl alcohol 0.90 Fragrance 1.40 Dyes and others 1.10 Purified water 15.50 Next, the effects of using the cosmetic of this invention will be explained. (i) Test method Twenty women each between the ages of 30 and 40 with severe rough skin, those with dark spots, and those with severe itching were selected as test subjects. The cream with the formulation of Example 2 was applied continuously to the rough and blemished skin group twice in the morning and evening for two months, and to the itchy skin group twice in the morning and evening for one month, and then the transparent soap with the formulation of Example 5 was applied. was used once a day during bathing for two months on a rough skin group and a blemish group, and its effects were investigated using the following method. That is, for each symptom, the 5 shown in Table 1 below.
A graded evaluation standard was created, and the symptoms before and after the use test were graded as shown in Table 1.
【表】【table】
【表】
そして使用試験前の症状と試験終了後の症状
とを比較して、3段階以上改善効果のあつたも
のを著効、2段階改善効果のあつたものを有
効、1段階の改善効果のあつものをやや有効、
不変もしくは悪化したものを無効として、集計
した結果、下記第2〜6表の結果が得られた。[Table] Comparing the symptoms before the test and the symptoms after the test, those with an improvement effect of 3 or more levels are markedly effective, those with a 2 level improvement effect are effective, and those with a 1 level improvement effect. Slightly effective,
The results shown in Tables 2 to 6 below were obtained by counting those that remained unchanged or deteriorated as invalid.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】
(ii) 試験効果
上記の表のように、著効と有効とを合して有
効群とし、やや有効と無効とを合して無効群と
して2分した場合、この発明の化粧料のクリー
ムと透明石けんは、肌あれについては美容上重
要な化粧のり効果も含めて有効率65%という優
れた改善効果を示し、また無効群に含まれるも
のでもやや有効の例が多かつた。このことか
ら、この発明の多糖類が皮膚に活力を与えかつ
しつとりとしたうるおいを与える保水性を有す
ると考えられる。
またかゆみについてはクリームが有効率55%
という優れた改善効果を示した。
さらに従来改善がむつかしいとされていたし
みについては、クリームと石けんがそれぞれ35
%と40%の有効率を示した。
なお上記の効果の外に、この発明の多糖類が
毛髪に対しても活力とうるおいを与えることが
認められた。
上記の結果から明らかなように、この発明の
薬用ニンジン多糖類含有の化粧料はすぐれた美
容効果を有する[Table] (ii) Test effect As shown in the table above, when the cosmetics of this invention are divided into two groups: markedly effective and effective are combined into an effective group, and moderately effective and ineffective are combined into an ineffective group. The cream and transparent soap showed an excellent improvement effect on rough skin, with an effectiveness rate of 65%, including the cosmetically important effect of applying makeup, and even those in the ineffective group were slightly effective in many cases. From this, it is considered that the polysaccharide of the present invention has water-retaining properties that give vitality to the skin and keep it moisturized. Also, creams have a 55% effectiveness rate for itching.
This showed an excellent improvement effect. Furthermore, for stains that are conventionally considered difficult to improve, cream and soap each have 35%
% and showed an efficacy rate of 40%. In addition to the above-mentioned effects, the polysaccharide of the present invention was also found to impart vitality and moisture to the hair. As is clear from the above results, the cosmetic containing medicated ginseng polysaccharide of this invention has excellent beauty effects.
Claims (1)
エーテル、ベンゼン、クロロホルム及びアセト
ンに不溶 (iii) 1%水溶液のPHは約5.5 (iv) 分解温度 約218℃ (v) 2%フエノール水溶液と濃硫酸との混液で淡
黄赤色を呈しかつ銀鏡反応とフエーリング試液
に陽性 を有することによつて特徴づけられる多糖類を有
効成分として含有することを特徴とする化粧料。 2 薬用ニンジンがオタネニンジン(パナツク
ス・ギンセング、シー・エー・メイヤー)、トチ
バニンジン(パナツクス・ヤポニクス、シー・エ
ー・メイヤー)、アメリカニンジン(パナツク
ス・キンキエホリウム、リンネ)、三七ニンジン
(パナツクス・ノトギンセング、バーキルまたは
パナツクスプソイドギンセング、ワーリツヒ)で
ある特許請求の範囲第1項記載の化粧料。 3 薬用ニンジンがオタネニンジンである特許請
求の範囲第2項記載の化粧料。 4 薬用ニンジンの各糖類が0.001〜3重量%配
合されてなる特許請求の範囲第1項記載の化粧
料。 5 薬用ニンジンの多糖類が0.01〜0.5重量%配
合され剤形が石けんである特許請求の範囲第4項
の化粧料。[Claims] 1. Contained in medicinal ginseng and having the following properties: (i) Has a skin activating effect (ii) Soluble in water, sparingly soluble in methanol, ethanol,
Insoluble in ether, benzene, chloroform and acetone (iii) PH of 1% aqueous solution is approximately 5.5 (iv) Decomposition temperature approximately 218℃ (v) A mixture of 2% phenol aqueous solution and concentrated sulfuric acid exhibits a pale yellow-red color and a silver mirror reaction. 1. A cosmetic containing as an active ingredient a polysaccharide characterized by having a positive result in Fehling's test solution. 2. Medicinal ginseng is Panax ginseng (Panatucus ginseng, C.A. Mayer), Panax ginseng (Panatchus japonicus, C.A. Mayer), American ginseng (Panatux quinquefolium, Linnaeus), Panax ginseng (Panatchus notoginseng, Burkill or 2. The cosmetic composition according to claim 1, wherein the cosmetic composition is Panax pseudoginseng, Warritsch). 3. The cosmetic according to claim 2, wherein the medicinal ginseng is Panax ginseng. 4. The cosmetic according to claim 1, which contains 0.001 to 3% by weight of each saccharide of medicinal ginseng. 5. The cosmetic according to claim 4, which contains 0.01 to 0.5% by weight of medicated ginseng polysaccharide and is in the form of a soap.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59235423A JPS61115013A (en) | 1984-11-08 | 1984-11-08 | Cosmetic |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59235423A JPS61115013A (en) | 1984-11-08 | 1984-11-08 | Cosmetic |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61115013A JPS61115013A (en) | 1986-06-02 |
| JPH0138762B2 true JPH0138762B2 (en) | 1989-08-16 |
Family
ID=16985882
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59235423A Granted JPS61115013A (en) | 1984-11-08 | 1984-11-08 | Cosmetic |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61115013A (en) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63112690A (en) * | 1986-10-30 | 1988-05-17 | Fumio Honma | Production of combustion improver for petroleum fuel |
| JPS63198609A (en) * | 1987-02-14 | 1988-08-17 | Eikoudou:Kk | Cosmetic |
| JP2001151663A (en) * | 1999-11-25 | 2001-06-05 | Iho Tokuma | Method for extracting silk essence, extracted solution of silk essence, beauty solution, soap and shampoo containing the extracted solution of silk essence |
| KR100423521B1 (en) * | 2001-08-29 | 2004-03-18 | 네비온 주식회사 | Cosmetic compositions containing panax ginseng polysaccharides |
| KR100479803B1 (en) * | 2002-04-08 | 2005-03-30 | 홍림통산(주) | Composition containing an extract of specially treated ginseng for preventing brain cells and treating brain stroke |
| WO2004017980A1 (en) * | 2002-08-26 | 2004-03-04 | Taisho Pharmaceutical Co.,Ltd | Whitening agent |
| US7585518B2 (en) | 2002-11-19 | 2009-09-08 | Kimberly-Clark Worldwide, Inc. | Products and methods for maintaining or increasing ceramide levels in skin |
| JP5264106B2 (en) * | 2007-06-01 | 2013-08-14 | 小林製薬株式会社 | Composition having antioxidative action |
| JP5264107B2 (en) * | 2007-06-01 | 2013-08-14 | 小林製薬株式会社 | Composition having antioxidative action |
| JP5261457B2 (en) * | 2010-09-13 | 2013-08-14 | 花王株式会社 | Cathepsin D production promoter |
-
1984
- 1984-11-08 JP JP59235423A patent/JPS61115013A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61115013A (en) | 1986-06-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |