JP2006028150A - Skin elasticity activation cosmetic - Google Patents

Skin elasticity activation cosmetic Download PDF

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JP2006028150A
JP2006028150A JP2004236865A JP2004236865A JP2006028150A JP 2006028150 A JP2006028150 A JP 2006028150A JP 2004236865 A JP2004236865 A JP 2004236865A JP 2004236865 A JP2004236865 A JP 2004236865A JP 2006028150 A JP2006028150 A JP 2006028150A
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skin
skin elasticity
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wrinkles
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Fumiyuki Terada
文行 寺田
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Abstract

<P>PROBLEM TO BE SOLVED: To prepare a cosmetic that can activate skin elasticity unavoidably lowered by aging or accumulation of the ultraviolet stimulation, not by skin humidity retention, without reliance on uncertain percutaneous absorption or forced injection of a dermal elastic fiber material. <P>SOLUTION: Panax pseudoginseng wall extract and/or Panax pseudoginseng wall bud extract and/or a saponin fraction from the Panax pseudoginseng wall bud extract is contained in the cosmetic as active ingredient. The cosmetic is applied to the skin, thereby preventing the skin from lowering skin elasticity or improving and activating the skin elasticity. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は皮膚弾力性賦活化粧料にかかわり、その目的は加齢や紫外線刺激など様ざまな原因の蓄積で低下する皮膚弾力性を賦活する、生薬である三七(Panax pseudoginseng wall)抽出物、及びまたは三七花莟部抽出物、及びまたは三七花莟部抽出物のサポニン分画成分を有効成分とする安全性すぐれた皮膚弾力性賦活化粧料を提供することにある。  The present invention relates to skin elasticity activating cosmetics, the purpose of which is a herbal medicine, Panax pseudogonseng extract, which activates skin elasticity that decreases due to accumulation of various causes such as aging and ultraviolet ray stimulation, Another object of the present invention is to provide a skin elasticity activating cosmetic with excellent safety, comprising as an active ingredient the saponin fraction component of the nanaka bud extract and / or the nanaka bud extract.

皮膚の弾力性とくに成人女性顔面のそれは、加齢により不可避的に低下する。しかもその低下度は、成人に至るまでの顔面曝光時間の累積にも相関するから、皮膚弾力性低下のあらわれである顔面各部位のしわの予防、改善は過去の皮膚ダメージの遡及挽回という点からも容易でない。従来そのことの対策には専ら化粧料、化粧法の工夫が充てられてきたが、その効果はほとんど不鮮明で、現在のところ、化粧料、化粧法による対策は、効果の期待よりも、何もしなければ皮膚弾力性低下が加速するという不安により行われている。  Skin elasticity, especially that of adult female faces, inevitably decreases with age. Moreover, the degree of reduction correlates with the accumulation of facial exposure time up to adulthood, so the prevention and improvement of wrinkles in each part of the face, which is a manifestation of skin elasticity reduction, is a retroactive recovery of past skin damage. Is not easy. Conventionally, cosmetics and makeup methods have been exclusively devised for countermeasures, but the effects are almost unclear, and at present, the countermeasures by cosmetics and makeup methods do nothing more than expected effects. Otherwise, it is done because of anxiety that the skin elasticity decline will accelerate.

皮膚弾力性低下とそのあらわれであるしわの予防、改善に用いられている化粧料には、皮膚外部からの保湿と、皮膚内部からの弾力性補強が方法として採られている。成人女性は加齢に従い女性ホルモン分泌が漸減し、それは皮膚の乾燥につながるから、より効果的な保湿剤を化粧料に配合して、皮膚の水分蒸散を防ぐのである。保湿剤としては、例えばコンドロイチン硫酸ナトリウム、1,3−ブチレングリコール、乳酸ナトリウム、マルチトール、キシリトール、ビファミン(Vifamine)、ソルビトール、グリセリン、アミノ酸(セリン、スレオニンなど)、コラーゲンほか多種のものがある。いわば皮膚のコーティング剤の用をなす。一方皮膚内部からの弾力性補強は、表皮と皮下組織をつなぐ真皮の弾力線維構築を目的とするもので、膠原線維である動物性コラーゲン、植物性コラーゲン、海洋性コラーゲン、構造蛋白質であるエラスチン、弾力線維を充填するヒアルロン酸(高分子多糖)など各物質の真皮内送りこみをはかる。但し、いうまでもなく表皮はそのウォーターバリアにより水溶性物質の、また分子量大なるものの吸収を許さず、またそれら物質の極小断片化や吸収条件の工夫で、仮に稀に吸収されることあったとしても、それらが自動的に真皮内で弾力線維に再構築されることは望めないので、化粧料に弾力線維材料を配して、皮膚弾力性低下の予防、改善を得ることは難しい。  The cosmetics used for the prevention and improvement of wrinkle, which is a decrease in skin elasticity and its appearance, employ moisture retention from the outside of the skin and elasticity reinforcement from the inside of the skin. Adult women gradually decrease female hormone secretion as they age, which leads to dry skin, so more effective moisturizers are added to cosmetics to prevent skin moisture transpiration. Examples of the humectant include sodium chondroitin sulfate, 1,3-butylene glycol, sodium lactate, maltitol, xylitol, bifamin (Vifamine), sorbitol, glycerin, amino acids (serine, threonine, etc.), collagen, and various other types. In other words, it is used as a skin coating agent. On the other hand, elastic reinforcement from the inside of the skin is intended for the construction of elastic fibers in the dermis that connects the epidermis and subcutaneous tissue. Collagen fibers such as animal collagen, plant collagen, marine collagen, structural protein elastin, Intradermal delivery of substances such as hyaluronic acid (polymer polysaccharide) that fills elastic fibers. However, it goes without saying that the epidermis does not allow the absorption of water-soluble substances or substances with a large molecular weight due to its water barrier, and it was rarely absorbed due to minimal fragmentation of the substances and devising the absorption conditions. Even so, since it cannot be expected that they are automatically reconstructed into elastic fibers in the dermis, it is difficult to prevent or improve skin elasticity by arranging elastic fiber materials in cosmetics.

皮膚の弾力性は表皮の下層にある真皮の弾力線維構造に支えられている。はじめ細胞内で合成されたコラーゲンはきわめて不安定だが、細胞外分泌に伴いコラーゲンを構成するポリペプチド鎖が三重ヘリックス構造を形成して安定化し、弾力線維と共に立体構造をつくり、ヒアルロン酸の充填を得て弾力性をもつに至る。弾力性の喪失は、紫外線などの刺激で立体構造が壊れ、機能を失した弾力線維を代償するため過産生された非構造的(コラーゲンと立体構造をつくらない)弾力線維が、結合組織における密着性を阻んで、皮膚を緩ませ、すなわち皮膚弾力性を低下させしわをふやしていくのである。皮膚外からのコラーゲンなどが、真皮内に至って、何らかのエネルギーなしに、以上のような過程を経て、自動的に皮膚弾力性を改善、賦活し得ないとする所故である。  The elasticity of the skin is supported by the elastic fiber structure of the dermis in the lower layer of the epidermis. Collagen initially synthesized in cells is extremely unstable, but the polypeptide chains that make up collagen are stabilized by forming a triple helix structure along with extracellular secretion, creating a three-dimensional structure with elastic fibers, and obtaining hyaluronic acid filling And has elasticity. Loss of elasticity is caused by non-structural (non-formation of collagen and 3D structure) elastic fibers in order to compensate for elastic fibers that have lost their function due to the destruction of the 3D structure by stimuli such as ultraviolet rays. It obstructs sex and loosens the skin, that is, reduces skin elasticity and softens wrinkles. This is because collagen or the like from outside the skin reaches the inside of the dermis and does not automatically improve or activate the skin elasticity through the above process without any energy.

化粧法による皮膚弾力性改善法は、主にエステティック施術として行われる。それはパックやピーリングといった物理的で一過的な方法による。たるみを引き上げ、一時的にしわを目立たなくするこの方法は、いうまでもなく、皮膚弾力性を賦活する方法とは言い難く、誰もが日常に為しうる簡便さにも遠い。  The skin elasticity improving method by a cosmetic method is mainly performed as an esthetic treatment. It is based on physical and transient methods such as packing and peeling. Needless to say, this method of raising sagging and temporarily making wrinkles inconspicuous is not a method of activating skin elasticity, and is far from convenient for everyone.

皮膚弾力性低下のあらわれであるしわ、とくに女性顔面のそれは筋の弾力性低下という原因はともかく、顔面各部位における成因は同じでない。  Wrinkles, which are manifestations of skin elasticity reduction, especially on the female face, are not the same cause of each facial part, regardless of the cause of muscle elasticity reduction.

前述のように、加齢によってコラーゲン線維は少なくなり、紫外線などの刺激で弾力線維は分断化され、これの線維からなる立体構造をうめていたヒアルロン酸は充填の役をはたせず、徒らに水分をあつめてむくみのもととなる。はりや弾みを失して、皮膚は密着性を減じ、瞼などに「細かいしわ」をつくるようになる。また筋肉の動きが、密着性を減じた皮膚にくせをつけて、ひたいやみけんに「大きいしわ」をつくり、さらに細かいしわや大きいしわに連動伸縮し難くなった目尻や頬などに「表情しわ」がふえていくのである。  As mentioned above, collagen fibers decrease with aging, elastic fibers are fragmented by stimuli such as ultraviolet rays, and hyaluronic acid filled with a three-dimensional structure composed of these fibers does not serve as a filler. It becomes the source of swelling by collecting moisture. Loss of elasticity and resilience causes the skin to lose its adhesiveness and create fine wrinkles on wrinkles. In addition, the movement of the muscles creates a “large wrinkle” in the skin and the skin that has reduced adhesion, and “facial wrinkles” on the corners of the eyes and cheeks that are difficult to expand and contract in conjunction with fine wrinkles and large wrinkles. "

これらのしわに対する従来技術は、前述の化粧料や化粧法の他に、医療における対策としては次のような方法が一般に行われている。すなわち「細かいしわ」にはレーザーピーリングが施される。レーザーによって表皮や真皮を一度変性させ(表皮はなくなり、真皮も水分を失って萎縮する)、約一週間後に新しい表皮を再生させ、真皮においても、線維構造を自ら新しくつくらせるのである。もちろん麻酔が必要で、表皮再生後も約一ヶ月発赤や色素沈着が残ることがある。  In the prior art for these wrinkles, in addition to the cosmetics and makeup methods described above, the following methods are generally performed as medical measures. In other words, laser peeling is applied to “fine wrinkles”. Lasers denature the epidermis and dermis once (the epidermis disappears and the dermis loses moisture and atrophy), and after about a week, the new epidermis is regenerated, and in the dermis, a new fiber structure is created. Of course, anesthesia is required, and redness and pigmentation may remain for about one month after epidermis regeneration.

「大きいしわ」には、ひたいの横じわやみけんの縦じわの溝にそって、コラーゲンやヒアルロン酸を注入する。コラーゲンなどは皮膚外塗で吸収され難いからであるが、しわ改善効果は約6ヶ月持続するもののアレルギー発生率は約3%と低くない。  Collagen and hyaluronic acid are injected into the “large wrinkles” along the groove of the horizontal wrinkles of the sun and the vertical wrinkles of the soap. This is because collagen and the like are difficult to be absorbed by the skin external coating, but the wrinkle improving effect lasts for about 6 months, but the allergy incidence is not as low as about 3%.

「表情しわ」にはボツリヌス菌毒素の微量注入が有効とされる。顔にある約20種類の表情筋のうち、特定筋への神経伝達を遮断し、表情しわができないようにするのだが、ボツリヌス菌毒素は食中毒原因物質でもあるので、医師の管理下以外の場合に行える方法ではない。  Microinjection of Clostridium botulinum toxin is effective for “facial wrinkles”. Of the approximately 20 types of facial muscles on the face, it blocks nerve transmission to specific muscles and prevents facial wrinkles. However, since Clostridium botulinum toxin is also a food poisoning agent, it is not under the control of a doctor. It is not a method that can be done.

外塗してしわを少なくし、皮膚新生を促すものにトレチノインがある。これは活性型ビタミンA物質で表皮の新陳代謝を倍速する。約4週間である表皮のターンオーバー(表皮新生から角化角解までのプロセス)時間を約2週間に縮めるので塗布部位の発赤、炎症、角質脆弱化を避け難く、これをふつうの化粧料使用の感覚で用いることはできない。  Tretinoin is one that can be applied externally to reduce wrinkles and promote skin formation. This is an active vitamin A substance that doubles the metabolism of the epidermis. It takes about 4 weeks to shorten the epidermis turnover (process from epidermis formation to keratinization) to about 2 weeks, so it is difficult to avoid redness, inflammation and keratin weakening at the application site. Cannot be used with the sense of

以上に述べたように、加齢あるいは紫外線刺激など生存上不可避的な要因で、皮膚弾力性は低下し、顔面などでのしわは増していくのであるが、とくに成人以降の女性において、このことが美容的に、また精神的に多大のストレスを呈するので、ふるくから不断に、その予防、改善の方策が講じられ努力が続けられている。従来技術においては、このことに効果的な方法がなく、唯一効果ありとされる方法も、高率に副作用を伴いやすいので、一般人がプライベイトにスキンケア的感覚で行いうるものではない。  As mentioned above, skin elasticity decreases and wrinkles on the face increase due to unavoidable factors such as aging or UV stimulation, but this is particularly true in women after adults. Presents a great deal of stress both cosmetically and mentally, and measures are being taken to prevent and improve it constantly. In the prior art, there is no effective method for this, and the only effective method is likely to be accompanied by side effects at a high rate, so that it cannot be performed privately by a skin care sensation.

本発明者は従来技術におけるこのような状況をふまえ、皮膚弾力性賦活における三七(Panax pseudoginseng wall)抽出物含有化粧料及びまたは三七花莟部抽出物含有化粧料及びまたは三七花莟部抽出物のサポニン分画成分含有化粧料の効果研究を重ね本発明を為すに至ったものである。  In view of such a situation in the prior art, the inventor of the present invention has included cosmetics containing Panax pseudogingens wall extract and / or Sansana part extract-containing cosmetics and / The present invention has been made through repeated studies on the effects of cosmetics containing a saponin fraction component of the extract.

すなわち請求項1にかかわる発明は、生薬である三七(Panax pseudoginseng wall)からの抽出物を有効成分として含有することを特徴とする皮膚弾力性賦活化粧料に関する。
請求項2にかかわる発明は、生薬である三七(Panax pseudoginseng wall)からの抽出物が三七の花莟部からの抽出物であることを特徴とする請求項1の皮膚弾力性賦活化粧料に関する。
請求項3にかかわる発明は、生薬である三七(Panax pseudoginseng wall)花莟部からの抽出物が、そのサポニン分画成分であることを特徴とする請求項1乃至2記載の皮膚弾力性賦活化粧料に関する。
That is, the invention according to claim 1 relates to a skin elasticity activating cosmetic characterized by containing, as an active ingredient, an extract from a herbal medicine, Panax pseudogingens wall.
The invention according to claim 2 is characterized in that the extract from Panax pseudoginseng wall, which is a herbal medicine, is an extract from the floret part of the seven, About.
The invention according to claim 3 is characterized in that the extract from the floret part of the panax pseudogonseng wall which is a crude drug is a saponin fraction component thereof. Regarding cosmetics.

本発明の皮膚弾力性賦活化粧料は、三七(Panax pseudoginseng wall)抽出物及びまたは三七(Panax pseudoginseng wall)花莟部抽出物、及びまたは三七(Panax pseudoginseng wall)花莟部抽出物サポニン分画成分を化粧料基剤に含有せしめ、外塗経皮的に皮膚弾力性低下を予防し、改善し、皮膚弾力性賦活をはかるもので、皮膚弾力性低下によるしわ、とくに女性顔面のそれの予防、改善に、日常簡便に用い得て効果あり安全性もたかい。  The skin elasticity activating cosmetic composition of the present invention comprises a panax pseudodogseng extract and / or a panax pseudoseng wall extract, or a panax pseudoginseng flower extract. Incorporates a fractionation component into a cosmetic base to prevent and improve skin elasticity through skin coating, and to improve skin elasticity. Wrinkles caused by skin elasticity decrease, especially those of female faces It can be used easily for daily prevention and improvement, and is effective and safe.

本発明における皮膚弾力性賦活化粧料は、化粧料としての何れの形態をも採りうるが、とりわけ基礎化粧品類であるクリーム、ジェル(クリーム、ローション)、ローション、乳液、パックなど、メイクアップ化粧品類であるおしろい類、口紅類、頭髪用化粧品類であるシャンプー、リンス、トリートメント、トニック、育毛剤などの形態が好適に選ばれる。  The skin elasticity activating cosmetic of the present invention can take any form as a cosmetic, but makeup cosmetics such as creams, gels (creams, lotions), lotions, emulsions, packs, etc., which are basic cosmetics, among others. The forms of shampoos, rinses, treatments, tonics, hair restorers, etc., which are fungis, lipsticks, and hair cosmetics are preferably selected.

本発明における皮膚弾力性賦活化粧料に含有せしめる三七は、生薬である三七(Panax pseudoginseng wall)すなわちウコギ科Araliaceae人参三七の根茎乾燥物で田三七(デンサンシチ)、田七(デンシチ)とも称される。
主たる成分は三七サポニンA(C305210)、三七サポニンB(C233810)Flavon配糖体などで、止血(出血血液の凝固時間を短縮し、血管を収縮する)、消炎、冠血流量増加(同時に心筋の酸素消費量を減少させる)、抗ウィルス、抗真菌などの作用が知られており、とくに血液流状改善(血液粘度低下、赤血球変形能賦活による)の働きにすぐれる。三七は止血作用にすぐれるとされ、事実その目的で賞用されるが、それは止血時間が短いのに血流をなめらかにするという二律反的な利点を有するからである。
In the present invention, the skin elasticity activating cosmetic contains the seventy-three (7) Panax pseudoginseng wall, that is, the dried rhizome of Arachaceae Aralaceae ginseng. Also called.
The main ingredients are 37 saponin A (C 30 H 52 O 10 ), 37 saponin B (C 23 H 38 O 10 ) Flavon glycoside, etc., and hemostasis (reducing the coagulation time of bleeding blood and contracting blood vessels) ), Anti-inflammation, increased coronary blood flow (decrease myocardial oxygen consumption at the same time), antiviral, antifungal and other actions are known, especially blood flow improvement (by reducing blood viscosity, erythrocyte deformability activation) Excellent at working. Thirty-seven is said to be superior in hemostatic action, and in fact is used for that purpose, because it has the dual advantage of smoothing blood flow despite its short hemostasis time.

本発明において用いる三七花莟部抽出物は、三七(Panax pseudoginseng wall)の花莟部乾燥物による。主たる成分は前述の三七根茎部と同じながら、生薬としての用途はいささか異なり、清熱(消炎)、鎮痛、降圧、それに頭昏、目眩、耳鳴、咽頭炎などの緩解に利用されている。  The three-necked flower bud extract used in the present invention is a dried flower bud part of a three-necked (Panax pseudogonseng wall). The main ingredient is the same as the above-mentioned 37th rhizome, but its use as a herbal medicine is slightly different, and it is used for relieving cleansing (anti-inflammatory), analgesic, antihypertensive, scalp, dizziness, tinnitus, pharyngitis, etc.

同じく本発明で用いられる三七花莟部抽出物のサポニン分画成分は抽出物の富サポニン分画成分で、トリテルペノイドサポニンであるダンマラン型サポニン(Dammarane Types aponin)を主に含有する。但し通常生薬として三七抽出物を抽出する場合には、この分画はその発泡性を嫌って除去されることが少なくない。  Similarly, the saponin fraction component of the extract of the nanaka bud part used in the present invention is a rich saponin fraction component of the extract, and mainly contains dammarane type saponin (Dammarane Types saponin) which is a triterpenoid saponin. However, when a 37 extract is extracted as a normal crude drug, this fraction is often removed because of its foaming property.

本発明の皮膚弾力性賦活化粧料調製においては、上記の三七抽出物、及びまたは三七花莟部抽出物、及びまたは三七花莟部抽出物のサポニン分画成分などの配合に加え、通常化粧料に用いられる各種原料、成分を適宜任意に用いて剤型を整えることも差支えない。それら原料、成分にはとくに限定ないが、通常化粧料(医薬部外品を含む)に用いられる公知の原料、成分、例えば油脂類、ロウ類、炭化水素、脂肪酸類、アルコール類、多価アルコール類、エステル類、天然高分子化合物、界面活性剤、酸化防止剤、金属イオン封鎖剤、pH調製剤、合成有機塩類、保湿剤、香料、ビタミン類、酵素類、有機薬品類、無機薬品類。動植物抽出成分、ガム質、アミン・アミド・金属石鹸、ホルモン類、抗生物質、防腐殺菌剤、アミノ酸類などである。  In the preparation of the skin elasticity activating cosmetic of the present invention, in addition to the above-mentioned 37 extract, and / or 37 flower bud extract, or saponin fraction component of the 37 flower bud extract, There is no doubt that the dosage form is adjusted by appropriately using various raw materials and ingredients usually used in cosmetics. These raw materials and components are not particularly limited, but are known raw materials and components that are usually used in cosmetics (including quasi drugs) such as fats and oils, waxes, hydrocarbons, fatty acids, alcohols, polyhydric alcohols. , Esters, natural polymer compounds, surfactants, antioxidants, sequestering agents, pH adjusters, synthetic organic salts, humectants, fragrances, vitamins, enzymes, organic chemicals, inorganic chemicals. Animal and plant extract ingredients, gum, amine / amide / metal soap, hormones, antibiotics, antiseptics, amino acids, etc.

また本発明においての三七抽出物、及びまたは三七花莟部抽出物の皮膚弾力性賦活化粧料への配合量は0.07〜3.5重量%の範囲、好ましくは0.1〜1.5重量%であればよく、三七花莟部抽出物サポニン分画成分の皮膚弾力性賦活化粧料への配合量は0.05〜2.5重量%の範囲、好ましくは0.07〜2.0重量%を至適とする。  In addition, the amount of the 37 extract and / or the 37 flower bud extract in the present invention is in the range of 0.07 to 3.5% by weight, preferably 0.1 to 1%. The amount of the saponin fraction saponin fraction component added to the skin elasticity activating cosmetic is in the range of 0.05 to 2.5% by weight, preferably 0.07 to 2.0% by weight is optimal.

以下本発明を実施例により説明する。但し本発明は以下の実施例に何ら限定されるものではない。
(実施例1)
三七(Panax pseudoginseng wall)抽出物の調製
三七根茎細切物(水分量10%以下)75gに20倍量の50%エタノール液を加え2時間加温(80℃)還流抽出し、これを濾過して濾液を約1/10量に濃縮し、濃縮物を凍結乾燥し、約21gの褐色粉末を得た。
Hereinafter, the present invention will be described by way of examples. However, the present invention is not limited to the following examples.
Example 1
Preparation of Panax pseudogonseng wall extract Add 75 volumes of 50% ethanol solution to 75 g of chopped radish (water content of 10% or less) and extract under reflux for 2 hours by heating (80 ° C). The filtrate was concentrated to about 1/10 volume by filtration, and the concentrate was lyophilized to obtain about 21 g of a brown powder.

(実施例2)
三七(Panax pseudoginseng wall)花莟部抽出部の調製
実施例1の三七根茎細切物75gを、三七花莟部細切物(水分量10%以下)にかえたもので、抽出物として褐色粉末約23gを得た。
(Example 2)
Preparation of Panax pseudoginseng flower floret part extraction part 75 g of 37 radish cuts of Example 1 were replaced with 37 floret part cuts (water content of 10% or less). As a result, about 23 g of brown powder was obtained.

(実施例3)
三七(Panax pseudoginseng wall)花莟部抽出物サポニン分画成分の調製
三七花莟細切物(水分量10%以下)10gを70%メタノール80mlで30分間加温(80%)還流抽出し、濾過した濾液を減圧濃縮し、これを脱脂してのち、水飽和n−ブタノール60mlで3回抽出し、n−ブタノール層を減圧濃縮乾固して花莟部抽出物サポニン分画成分0.7gを得た。
Example 3
Preparation of saponin fraction component of Panax pseudogonseng wall saponin extract 10g of crumpled crumpled flower (moisture content 10% or less) was extracted by refluxing with 80ml of 70% methanol for 30 minutes (80%). The filtered filtrate was concentrated under reduced pressure, degreased and extracted three times with 60 ml of water-saturated n-butanol. The n-butanol layer was concentrated under reduced pressure to dryness, and the floret extract saponin fraction component 0. 7 g was obtained.

(実施例4)
試験に供する化粧料1
ジェル処方
グリセリン 10.0重量%(以下同)
1,3−ブチレングリコール 5.0
オクチルドデセス−25 1.0
(アクリル酸アクリル酸アルキル(C10−30)コポリマー 0.5
メチルパラベン 0.3
クエン酸 1.0
水酸化ナトリウム(pH調整) 適量
PEG−60水添ヒマシ油 1.0
実施例1の三七抽出物 1.0
水 残量
合計 100.0
Example 4
Cosmetics for test 1
Gel prescription glycerin 10.0% by weight (same below)
1,3-butylene glycol 5.0
Octilde Dess-25 1.0
(Alkyl acrylate (C10-30) copolymer 0.5
Methylparaben 0.3
Citric acid 1.0
Sodium hydroxide (pH adjustment) PEG-60 hydrogenated castor oil 1.0
37 extract of Example 1 1.0
Remaining water <br/> Total 100.0

(実施例5)
試験に供する化粧料2
実施例4のジエル処方中、実施例1の三七抽出物を除き、実施例2の三七花莟部抽出物1.0重量%を加入したもの。
(Example 5)
Cosmetics for test 2
In the jelly formulation of Example 4, except for the 37th extract of Example 1, 1.0% by weight of the 37th flower bud extract of Example 2 was added.

(実施例6)
試験に供する化粧料3
実施例4のジェル処方中、実施例1の三七抽出物を除き、実施例3の三七花莟部抽出物サポニン分画成分0.75重量%を加入したもの。
(Example 6)
Cosmetics for test 3
In the gel formulation of Example 4, except for the 37 extract of Example 1, 0.75% by weight of the saponin fraction saponin fraction of Example 3 was added.

(試験例1)
コラーゲンを分解するコラゲナーゼの活性を阻害する試験
ヤガイ製1型コラゲナーゼ活性測定キットを用いて、その手順に従い行う。
実施例2で得た三七花莟部抽出物を測定用緩衝液(0.4M NaCl,10mM CaCl,0.04% NaNをpH7.5の0.1M Tris HClで希釈)で濃度調整して用いI型コラーゲン分解率を求め、コントロール(測定用緩衝液のみ)でのコラーゲン分解率に対する分解率割合より三七花莟部抽出物のコラゲナーゼ活性阻害率を求めた。なお比較例としてはコラゲナーゼ活性阻害作用物質であるエチレンジアミン4酢酸(EDTA)についても上記と同様に処理した。結果を表1に示す。
(Test Example 1)
Test for inhibiting the activity of collagenase which degrades collagen Using a kit for measuring type 1 collagenase activity manufactured by potato, the procedure is carried out.
Concentration adjustment of the extract of the 37 flower buds obtained in Example 2 with a buffer for measurement (0.4 M NaCl, 10 mM CaCl 2 , 0.04% NaN 3 diluted with 0.1 M Tris HCl at pH 7.5) Then, the collagen type I decomposition rate was determined, and the collagenase activity inhibition rate of the extract of the 37th flower bud was determined from the rate of the degradation rate relative to the collagen degradation rate in the control (measurement buffer only). As a comparative example, the same treatment was applied to ethylenediaminetetraacetic acid (EDTA), which is a collagenase activity inhibitory agent. The results are shown in Table 1.

Figure 2006028150
Figure 2006028150

(試験例2)
実施例4,5,6の化粧料使用による効果を次の基準により評価した。すなわち成人女性15人(29〜46才)を三群に分け、各5人ずつ実施例4,5,6の化粧料を就寝前洗顔後の顔面に塗布せしめ、4週間の使用期間前後の顔のしわの状態を比較した。基準において二段階以上の改善を有効、一段階の改善をやや有効、その他を無効とした。結果を表2に示す。(なお試験参加15人全員において、試験期間中及び試験後2週間のあいだ発赤、かゆみをはじめ、何らかの顔面皮膚異常も認められなかった。)
(Test Example 2)
The effects of using cosmetics in Examples 4, 5, and 6 were evaluated according to the following criteria. That is, 15 adult women (29 to 46 years old) are divided into three groups, and each of the five is applied with the cosmetics of Examples 4, 5, and 6 on the face after washing before sleeping. The state of wrinkles was compared. Two or more improvements in the standard were effective, one improvement was somewhat effective, and others were disabled. The results are shown in Table 2. (Note that in all 15 participants in the study, no facial skin abnormalities were observed, including redness and itching during the study period and for 2 weeks after the study.)

(評価基準)
5〜目尻、下瞼にしわが目立ち,下瞼にかいこ状のむくみがみえる。
4〜下瞼内角がすすけた感じで、目尻にもしわがみえる。
3〜下瞼にむくみやすすけた感じはないが、共にしわがみえる。
2〜表情を動かせると下瞼、目尻にしわがみえる。
1〜下瞼、目尻に気になるほどのしわはみえない。
(Evaluation criteria)
5 Wrinkles are conspicuous in the corners of the eyes and under the armpits, and a swollen shape appears in the armpits.
4-The inner corner of the lower eyelid is refreshing, and wrinkles can be seen in the corners of the eyes.
3-There is no feeling of swelling or mottling in the lower arm, but wrinkles can be seen together.
2 If you can move the expression, wrinkles will appear in the lower eyelids and the corners of the eyes.
No wrinkles that are worrisome in 1 to lower armpits and eyes.

Figure 2006028150
Figure 2006028150

表1、表2に示された結果から、実施例4,5,6の皮膚弾力性賦活化粧料は、皮膚弾力性低下の予防、改善、そして皮膚弾力性賦活にすぐれた効果をもつことがわかる。  From the results shown in Tables 1 and 2, the skin elasticity activating cosmetics of Examples 4, 5, and 6 have excellent effects in preventing and improving skin elasticity reduction and skin elasticity activation. Recognize.

以下本発明にかかわる皮膚弾力性賦活化粧料の処方例を示す。なお含有量は何れも重量%である。
処方例:クリーム、100g中
ステアリン酸 10.0
セタノール 2.0
ラノリン 1.0
ミリスチン酸イソプロピル 3.0
モノステアリン酸ポリエチレングリコール 1.5
トリエタノールアミン 0.8
香料 微量
ソルビトール(70%) 4.0
メチルパラベン 0.1
実施例1の抽出物 1.0
水 残部
Hereinafter, formulation examples of skin elasticity activating cosmetics according to the present invention will be shown. In addition, all content is weight%.
Formulation example: cream, stearic acid in 100 g 10.0
Cetanol 2.0
Lanolin 1.0
Isopropyl myristate 3.0
Polyethylene glycol monostearate 1.5
Triethanolamine 0.8
Fragrance Trace amount of sorbitol (70%) 4.0
Methylparaben 0.1
Extract of Example 1 1.0
Water balance

処方例:ローション、100g中
エタノール 15.0
モノラウリン酸POE(20)ソルビタン 1.0
1,3−ブチレングリコール 3.0
ソルビトール(70%) 2.0
ピロリドンカルボン酸ナトリウム 3.0
メチルパラベン 0.1
香料 微量
実施例2の抽出物 0.8
水 残部
Formulation example: lotion, ethanol in 100 g 15.0
Monolauric acid POE (20) sorbitan 1.0
1,3-butylene glycol 3.0
Sorbitol (70%) 2.0
Sodium pyrrolidonecarboxylate 3.0
Methylparaben 0.1
Fragrance Extract from Example 2 0.8
Water balance

処方例:乳液、100g中
トリオクタン酸グリセリン 10.0
ジカプリン酸ネオベンチルグリコール 8.0
セタノール 6.0
ヒドロキシステアリン酸コレステリル 1.0
ステアリン酸 3.0
パラベン 0.2
オクチルアクリルアミドアクリル樹脂 0.3
プロテアーゼ 0.1
1,3−ブチレングリコール 3.0
実施例3の三七サポニン分画成分 0.5
香料 微量
水 残量
Formulation example: emulsion, glycerin trioctanoate in 100 g 10.0
Diventric acid neobenchyl glycol 8.0
Cetanol 6.0
Cholesteryl hydroxystearate 1.0
Stearic acid 3.0
Paraben 0.2
Octylacrylamide acrylic resin 0.3
Protease 0.1
1,3-butylene glycol 3.0
37 saponin fraction component of Example 3 0.5
Perfume Trace water Remaining

Claims (3)

生薬である三七(Panax pseudoginseng wall)からの抽出物を有効成分として含有する事を特徴とする皮膚弾力性賦活化粧料  Skin elasticity activating cosmetic characterized in that it contains an extract from the herbal medicine Panax pseudodogseng wall as an active ingredient 生薬である三七(Panax pseudoginseng wall)からの抽出物が三七の花莟部からの抽出物である事を特徴とする請求項1の皮膚弾力性賦活化粧料  The skin elasticity activating cosmetic according to claim 1, wherein the extract from Panax pseudoseng wall is a herbal extract. 生薬である三七(Panax pseudoginseng wall)花莟部からの抽出物がそのサポニン分画成分であることを特徴とする請求項1乃至2記載の皮膚弾力性賦活化粧料  3. The skin elasticity activating cosmetic according to claim 1 or 2, wherein an extract from the bud part of a panax pseudogonseng wall is a saponin fraction component.
JP2004236865A 2004-07-20 2004-07-20 Skin elasticity activation cosmetic Pending JP2006028150A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE1027772A1 (en) 2019-11-21 2021-06-15 Botalys Sa COMPOSITION OF GINSENG TO IMPROVE SKIN CONDITION AND ITS USE FOR THE TREATMENT OF DERMATOLOGICAL DISEASES

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE1027772A1 (en) 2019-11-21 2021-06-15 Botalys Sa COMPOSITION OF GINSENG TO IMPROVE SKIN CONDITION AND ITS USE FOR THE TREATMENT OF DERMATOLOGICAL DISEASES

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