JP2007246492A - Humectant, cell activator and antioxidant - Google Patents

Humectant, cell activator and antioxidant Download PDF

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JP2007246492A
JP2007246492A JP2006075836A JP2006075836A JP2007246492A JP 2007246492 A JP2007246492 A JP 2007246492A JP 2006075836 A JP2006075836 A JP 2006075836A JP 2006075836 A JP2006075836 A JP 2006075836A JP 2007246492 A JP2007246492 A JP 2007246492A
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plant
antioxidant
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plants
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JP4994684B2 (en
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Akira Hatani
彰 葉谷
Yumiko Okumura
由美子 奥村
Hayashi Maeda
速 前田
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Noevir Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To obtain a humectant, a cell activator or an antioxidant that is obtained by finding an active ingredient having excellent moisture retaining action, cell activating action or antioxidant action and is widely applicable in the field of skin care preparation, food and beverage, etc. <P>SOLUTION: The humectant, the cell activator or the antioxidant comprises an extract of a plant of the family Fouquieriaceae having excellent moisture retaining action, cell activating action and antioxidant action. Various compositions exhibiting excellent moisture retaining action, cell activating action or antioxidant action are obtained by mixing an extract of plant of the family Fouquieriaceae with compositions of skin care preparation, food and beverage, etc. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

本発明は、保湿剤、細胞賦活剤、及び抗酸化剤に関する。さらに詳しくは、フォウクィエリア科植物の抽出物を含有する保湿剤、細胞賦活剤、及び抗酸化剤、並びにフォウクィエリア科植物の抽出物を含有する皮膚外用剤及び食品に関する。   The present invention relates to a humectant, a cell activator, and an antioxidant. More specifically, the present invention relates to a moisturizer, a cell activator, and an antioxidant containing an extract of a fulquiaceae plant, and an external preparation for skin and a food containing an extract of a focus area family.

加齢、紫外線、ストレスなどによるシワ、シミ、皮膚の弾性低下といった皮膚症状の要因として、乾燥、細胞機能低下、紫外線によるメラニン産生や色素沈着、真皮マトリックス成分の減少や変性、紫外線等による細胞の酸化傷害などが挙げられる。このような皮膚症状を防止・改善するために、様々な有効成分の検索及び配合検討が従来なされてきた。細胞賦活剤としては、ポンカンのエッセンス(特許文献1参照)、抗酸化剤としては、サルオガセ科サルオガセ属植物の抽出物(特許文献2参照)が知られている。   Causes of skin symptoms such as aging, ultraviolet rays, stress, wrinkles, stains, skin elasticity decrease, dryness, decreased cellular function, melanin production and pigmentation due to ultraviolet rays, decrease or degeneration of dermal matrix components, ultraviolet rays, etc. Examples include oxidative damage. In order to prevent and ameliorate such skin symptoms, search for various active ingredients and formulation studies have been conventionally conducted. As the cell activator, the essence of Ponkan (see Patent Document 1) is known, and as the antioxidant, an extract of the plant belonging to the genus Sarogase (see Patent Document 2) is known.

なお、フォウクィエリア科植物の抽出物を有効成分とする保湿剤、細胞賦活剤、及び抗酸化剤に関する先行技術は認められなかった。   In addition, the prior art regarding a moisturizer, a cell activator, and an antioxidant containing an extract of a fulquiaceae plant as an active ingredient was not recognized.

特開2001−131045号公報JP 2001-131045 A 特開平10−182413号公報Japanese Patent Laid-Open No. 10-182413

天然由来成分は、様々な薬理作用や美容効果を有することが知られ、これまでにも多数の植物や菌類などが皮膚外用剤や飲食品などの分野に幅広く応用されている。しかし、天然由来成分の中には未だその効果が知られていないものも数多く存在し、優れた保湿作用、細胞賦活作用、あるいは抗酸化作用を有する有効成分の開発が期待されていた。本発明は、このような有効成分を見出すためになされたものであり、皮膚外用剤や飲食品などの分野に幅広く応用が可能な保湿剤、細胞賦活剤、及び抗酸化剤を提供することを目的とする。   Naturally-derived components are known to have various pharmacological and cosmetic effects, and so far many plants and fungi have been widely applied to fields such as external preparations for skin and foods and drinks. However, there are many naturally-derived components whose effects are not yet known, and the development of an effective component having an excellent moisturizing action, cell activation action or antioxidant action has been expected. The present invention has been made in order to find such an active ingredient, and provides a moisturizer, a cell activator, and an antioxidant that can be widely applied to fields such as external preparations for skin and foods and drinks. Objective.

本発明者らは、皮膚外用剤や飲食品などの分野に幅広く応用が可能な保湿剤、細胞賦活剤、及び抗酸化剤を見出すために、天然由来の種々の物質について検討を行った。その結果、フォウクィエリア科植物の抽出物に優れた保湿作用、細胞賦活作用、及び抗酸化作用を見出し、さらに検討を重ね、本発明を完成するに至った。すなわち、本発明は、フォウクィエリア科植物を有効成分とする保湿剤、細胞賦活剤、及び抗酸化剤、並びにフォウクィエリア科植物の1種または2種以上の植物の抽出物を含有する皮膚外用剤及び食品を提供するものである。   In order to find a moisturizer, a cell activator, and an antioxidant that can be widely applied to fields such as external preparations for skin and foods and drinks, the present inventors have examined various naturally-derived substances. As a result, the present inventors have found an excellent moisturizing action, cell activation action, and antioxidant action for the extract of the Fauqueriaceae plant, and have further studied to complete the present invention. That is, the present invention relates to a skin containing a moisturizer, a cell activator, an antioxidant, and an extract of one or more plants of the focuiaceae family, comprising the fouciaceae family plant as an active ingredient. It provides external preparations and foods.

本発明によれば、優れた効果を有する保湿剤、細胞賦活剤、及び抗酸化剤を提供することができ、これらを皮膚外用剤や食品等の組成物に配合することにより、シワ、タルミ、肌のハリ、シミ、クスミといった種々の皮膚症状の防止や改善に優れた効果を発揮する様々な組成物を提供することができる。   According to the present invention, it is possible to provide a moisturizer, a cell activator, and an antioxidant that have excellent effects. By blending these into a composition such as a skin external preparation or food, wrinkles, tarmi, It is possible to provide various compositions that exhibit an excellent effect in preventing and improving various skin symptoms such as skin firmness, spots, and kusumi.

本発明の原料として用いられる植物であるフォウクィエリア科植物(Fouquieriaceae)は、フォウクィエリア属(Fouquieria)など11種の植物が知られている。フォウクィエリア属の植物としては、フォウクィエリア・コルムナリス(Fouquieria columnaris)、フォウクィエリア・スプレンデンス(Fouquieria splendens)、フォウクィエリア・ミクロフィラ(Fouquieria microphylla)、フォウクィエリア・シュレウェイ(Fouquieria shrevei)などが知られている。 It is a plant used as the raw material of the present invention Fou Quy area Plants (Fouquieriaceae) is Fou Quy area genus (Fouquieria) including 11 species of plants are known. The Fou Quy area plants of the genus, Fou Quy area Korumunarisu (Fouquieria columnaris), Fou Quy area Supurendensu (Fouquieria splendens), Fou Quy area micro Philadelphia (Fouquieria microphylla), Fou Quy area Schlesinger Way (Fouquieria shrevei) Etc. are known.

本発明に用いられる原料となる植物は、フォウクィエリア科植物であれば特に限定されないが、入手が比較的容易であることや有効性などの理由から、フォウクィエリア・ミクロフィラやフォウクィエリア・シュレウェイを用いることが特に好ましい。   The plant used as a raw material used in the present invention is not particularly limited as long as it is a foucoliaceae plant. However, for reasons such as availability and effectiveness, foucia area, microphylla and foucia area. -It is particularly preferable to use a shreway.

本発明におけるフォウクィエリア科植物の抽出物には、フォウクィエリア科植物の原体や乾燥物も抽出物に含まれるが、各種溶媒を用いて抽出した抽出物を用いるのが好ましい。抽出には、フォウクィエリア科植物の幹、枝、葉、花、種子、樹皮、樹液、根、茎、芽などのいずれの部位を用いても構わないが、簡便に利用するには葉を用いるとよい。抽出の際は、生のまま用いてもよいが、抽出効率を考えると、細切、乾燥、粉砕等の処理を行った後に抽出を行うことが好ましい。抽出は、抽出溶媒に浸漬するか、超臨界流体や亜臨界流体を用いた抽出方法でも行うことができる。抽出効率を上げるため、撹拌や抽出溶媒中でホモジナイズしてもよい。抽出温度としては、5℃程度から抽出溶媒の沸点以下の温度とするのが適切である。抽出時間は抽出溶媒の種類や抽出温度によっても異なるが、1時間〜14日間程度とするのが適切である。   In the present invention, the extract of the focus area family plant includes the active substance and the dried product of the focus area family plant, but it is preferable to use an extract extracted with various solvents. For extraction, you can use any part of the trunk, branch, leaf, flower, seed, bark, sap, root, stem, bud, etc. Use it. In the extraction, it may be used as it is, but considering the extraction efficiency, it is preferable to perform the extraction after performing processing such as shredding, drying, and pulverization. The extraction can be performed by immersing in an extraction solvent or by an extraction method using a supercritical fluid or a subcritical fluid. In order to increase the extraction efficiency, homogenization may be performed in stirring or an extraction solvent. The extraction temperature is suitably about 5 ° C. to the boiling point of the extraction solvent. The extraction time varies depending on the type of extraction solvent and the extraction temperature, but it is appropriate to set it to about 1 hour to 14 days.

抽出溶媒としては、水の他、メタノール、エタノール、プロパノール、イソプロパノール等の低級アルコール、1、3−ブチレングリコール、プロピレングリコール、ジプロピレングリコール、グリセリン等の多価アルコール、エチルエーテル、プロピルエーテル等のエーテル類、酢酸ブチル、酢酸エチル等のエステル類、アセトン、エチルメチルケトン等のケトン類などの溶媒を用いることができ、これらより1種又は2種以上を選択して用いる。また、生理食塩水、リン酸緩衝液、リン酸緩衝生理食塩水等を用いてもよい。さらに、水や二酸化炭素、エチレン、プロピレン、エタノール、メタノール、アンモニアなどの1種又は2種以上の超臨界流体や亜臨界流体を用いてもよい。   Extraction solvents include water, lower alcohols such as methanol, ethanol, propanol and isopropanol, polyhydric alcohols such as 1,3-butylene glycol, propylene glycol, dipropylene glycol and glycerin, ethers such as ethyl ether and propyl ether. , Solvents such as esters such as butyl acetate and ethyl acetate, and ketones such as acetone and ethyl methyl ketone can be used, and one or more of these can be selected and used. Further, physiological saline, phosphate buffer, phosphate buffered saline, or the like may be used. Furthermore, you may use 1 type, or 2 or more types of supercritical fluids and subcritical fluids, such as water, a carbon dioxide, ethylene, propylene, ethanol, methanol, ammonia.

フォウクィエリア科植物の上記溶媒による抽出物は、そのままでも使用することができるが、濃縮、乾固した物を水や極性溶媒に再度溶解して使用することもでき、これらの生理作用を損なわない範囲で脱色、脱臭、脱塩等の精製処理やカラムクロマトグラフィー等による分画処理を行った後に用いてもよい。フォウクィエリア科植物の前記抽出物やその処理物及び分画物は、各処理及び分画後に凍結乾燥し、用時に溶解して用いることもできる。   Extracts from the above-mentioned solvents of Fauqueriaceae plants can be used as they are, but the concentrated and dried solids can be used again by dissolving them in water or a polar solvent, which impairs their physiological functions. It may be used after performing purification treatment such as decolorization, deodorization, desalting, etc., or fractionation treatment by column chromatography or the like within a range. The said extract of Fauquiliaceae plant, its processed material, and the fractionation thing can also be freeze-dried after each processing and fractionation, and can also be melt | dissolved and used at the time of use.

フォウクィエリア科植物の抽出物は、優れた保湿作用、細胞賦活作用、及び抗酸化作用を有し、保湿剤、細胞賦活剤、及び抗酸化剤として利用することができる。また、フォウクィエリア科植物の抽出物を有効成分とする保湿剤、細胞賦活剤、及び抗酸化剤は、皮膚に外用するだけではなく、毛髪に利用することや経口摂取も可能であり、食品、飲料、あるいは医薬品などにも応用することが可能である。   The extract of Fauquiliaceae plant has excellent moisturizing action, cell activation action, and antioxidant action, and can be used as a moisturizing agent, cell activator, and antioxidant. In addition, moisturizers, cell activators, and antioxidants that contain extracts from Fouquilliaceae plants as active ingredients can be used not only for the skin but also for hair and can be taken orally. It can also be applied to beverages or pharmaceuticals.

フォウクィエリア科植物の抽出物を有効成分とする保湿剤は、皮膚や毛髪に対して優れた保湿作用を発揮し、特に皮膚に対する保湿効果が高い。   A moisturizing agent containing an extract of a fauqueriaceae plant as an active ingredient exhibits an excellent moisturizing effect on the skin and hair, and in particular has a high moisturizing effect on the skin.

フォウクィエリア科植物の抽出物を有効成分とする細胞賦活剤は、種々の細胞に対して優れた賦活作用を発揮するが、特に真皮線維芽細胞に対して優れた効果を発揮する。   A cell activator comprising an extract of a fauqueriaceae plant as an active ingredient exerts an excellent activation action on various cells, but particularly exhibits an excellent effect on dermal fibroblasts.

フォウクィエリア科植物の抽出物を有効成分とする抗酸化剤は、優れた抗酸化作用を発揮するが、特にフリーラジカル消去作用に優れた効果を発揮する。   Antioxidants containing an extract of a fulquiaceae plant as an active ingredient exhibit an excellent antioxidant effect, but in particular exhibit an excellent effect on free radical scavenging action.

また、フォウクィエリア科植物の抽出物を皮膚外用剤に配合することにより、シワ、タルミ、肌のハリ、シミ、クスミ、乾燥、小じわ等の皮膚症状の防止・改善に優れた効果を発揮する皮膚外用剤を得ることができ、保湿用皮膚外用剤あるいは老化防止改善用皮膚外用剤としても用いることができる。さらに、フォウクィエリア科植物の抽出物は、美容、健康維持、又は栄養補給を目的とするような食品にも用いることもできる。なお、本発明の食品には飲料も含まれる。   In addition, by blending the extract of Fauqueriaceae plant into the external preparation for skin, it exhibits an excellent effect in preventing and improving skin symptoms such as wrinkles, tarmi, skin firmness, spots, kumi, dryness, and fine wrinkles. A skin external preparation can be obtained, and can also be used as a moisturizing skin external preparation or a skin external preparation for anti-aging improvement. Furthermore, the extract of Fauqueriaceae plants can also be used for foods intended for beauty, health maintenance or nutritional supplementation. In addition, a drink is also contained in the foodstuff of this invention.

フォウクィエリア科植物の抽出物を皮膚外用剤に配合する際の配合量は、皮膚外用剤の種類や使用目的等によって調整することができるが、効果や安定性などの点から、全量に対して0.0001〜50.0重量%が好ましく、より好ましくは、0.001〜25.0重量%である。   The blending amount of the extract of Fauqueriaceae plant in the skin external preparation can be adjusted according to the type of skin external preparation and the purpose of use. 0.0001 to 50.0% by weight is preferable, and 0.001 to 25.0% by weight is more preferable.

フォウクィエリア科植物の抽出物を配合する皮膚外用剤の剤型は任意であり、例えば、ローションなどの可溶化系、クリームや乳液などの乳化系、カラミンローション等の分散系として提供することができる。さらに、噴射剤と共に充填したエアゾール、軟膏剤、粉末、顆粒などの種々の剤型で提供することもできる。   The dosage form of the external preparation for skin containing the extract of Fouquiria family plant is arbitrary, and for example, it can be provided as a solubilizing system such as lotion, an emulsifying system such as cream or emulsion, or a dispersing system such as calamine lotion. it can. Furthermore, it can also be provided in various dosage forms such as aerosols, ointments, powders and granules filled with a propellant.

なお、フォウクィエリア科植物の抽出物を配合する皮膚外用剤には、フォウクィエリア科植物の抽出物の他に、必要に応じて、通常医薬品、医薬部外品、皮膚化粧料、毛髪用化粧料及び洗浄料に配合される、油性成分、保湿剤、粉体、色素、乳化剤、可溶化剤、洗浄剤、紫外線吸収剤、増粘剤、薬剤、香料、樹脂、防菌防黴剤、アルコール類等を適宜配合することができる。また、本発明の効果を損なわない範囲において、他の保湿剤、細胞賦活剤、あるいは抗酸化剤との併用も可能である。   In addition to the extract of Fauquilia family plants, the preparation for external use for skin containing the extract of Fauquilia family plants usually contains drugs, quasi-drugs, skin cosmetics, and hair as needed. Oily ingredients, moisturizers, powders, pigments, emulsifiers, solubilizers, detergents, UV absorbers, thickeners, drugs, perfumes, resins, antibacterial and antifungal agents, blended in cosmetics and detergents, Alcohols etc. can be mix | blended suitably. Moreover, in the range which does not impair the effect of this invention, combined use with another moisturizer, a cell activator, or an antioxidant is also possible.

以下にフォウクィエリア科植物の抽出物の製造例、各作用を評価するための試験、皮膚外用剤や食品としての処方例、使用試験についてさらに詳細に説明するが、本発明の技術的範囲はこれによってなんら限定されるものではない。   In the following, a production example of an extract of Fouquilia family plant, a test for evaluating each action, a prescription example as a skin external preparation or food, and a use test will be described in more detail, but the technical scope of the present invention is This is not a limitation.

[製造例1]
フォウクィエリア科植物の乾燥粉砕物1kgに50重量%エタノール水溶液を10リットル加え、室温で7日間浸漬した。抽出液をろ過して回収し、溶媒を除去した後、フォウクィエリア科植物の抽出物を得た。
[Production Example 1]
10 kg of a 50 wt% aqueous ethanol solution was added to 1 kg of a dry pulverized product of Fauquiliaceae and immersed for 7 days at room temperature. The extract was collected by filtration, and after removing the solvent, an extract of Fauquiliaceae was obtained.

[製造例2]
フォウクィエリア科植物の乾燥粉砕物1kgに水を9リットル加え、90℃にて6時間還流して抽出した。抽出液をろ過して回収し、溶媒を除去した後、フォウクィエリア科植物の抽出物を得た。
[Production Example 2]
Nine liters of water was added to 1 kg of a dry pulverized product of Fauqueriaceae and extracted by refluxing at 90 ° C. for 6 hours. The extract was collected by filtration, and after removing the solvent, an extract of Fauquiliaceae was obtained.

[製造例3]
フォウクィエリア科植物の乾燥粉砕物1kgにメタノールを9リットル加え、室温で7日間浸漬した。抽出液をろ過して回収し、溶媒を除去した後、フォウクィエリア科植物の抽出物を得た。
[Production Example 3]
Nine liters of methanol was added to 1 kg of a dry pulverized product of Fauqueriaceae and immersed for 7 days at room temperature. The extract was collected by filtration, and after removing the solvent, an extract of Fauquiliaceae was obtained.

[製造例4]
超臨界抽出装置にフォウクィエリア科植物を投入し、40℃において15MPaの気圧下で二酸化炭素の超臨界流体を用いて抽出した。抽出物を回収し、フォウクィエリア科植物の抽出物を得た。
[Production Example 4]
A foucillaceae plant was introduced into a supercritical extraction apparatus, and extraction was performed using a supercritical fluid of carbon dioxide at 40 ° C. under a pressure of 15 MPa. The extract was collected to obtain an extract of the Fauqueriaceae plant.

まず、フォウクィエリア科植物の抽出物の細胞賦活作用について示す。試料には、フォウクィエリア・ミクロフィラの葉を製造例1により抽出したものを試料として評価を行った。   First, it shows about the cell activation effect | action of the extract of a Fauquilia family plant. The sample was evaluated by extracting the faux quillia microfila leaves according to Production Example 1 as samples.

評価は、以下の手順で行った。正常ヒト真皮線維芽細胞を1ウェル当たり2.0×10個となるように96穴マイクロプレートに播種した。播種培地には、ダルベッコ改変イーグル培地(DMEM)に1%のウシ胎児血清を添加したものを用いた。24時間培養後、任意の濃度の試料を添加した試験培地に交換し、さらに48時間培養した。次いで3−(4,5−ジメチル−2−チアゾリル)−2,5−ジフェニルテトラゾリウムブロミド(MTT)を400μg/mL含有する培地に交換して2時間培養し、テトラゾリウム環の開環により生じるフォルマザンを2−プロパノールにて抽出し、マイクロプレートリーダーにて550nmの吸光度を測定した。同時に濁度として650nmにおける吸光度を測定し、両測定値の差により細胞賦活作用を評価した。評価結果を、試料無添加のブランクにおける細胞賦活作用を100とした相対値にて表1に示す。なお、表中の*及び**は、t検定における有意確率P値に対し、有意確率1%未満(P<0.05)を*で有意確率1%未満(P<0.01)を**で表したものである。 The evaluation was performed according to the following procedure. Normal human dermal fibroblasts were seeded in a 96-well microplate at 2.0 × 10 4 cells per well. The seeding medium used was Dulbecco's modified Eagle medium (DMEM) supplemented with 1% fetal bovine serum. After culturing for 24 hours, the culture medium was replaced with a test medium to which a sample having an arbitrary concentration was added, and further cultured for 48 hours. Subsequently, the medium containing 400 μg / mL of 3- (4,5-dimethyl-2-thiazolyl) -2,5-diphenyltetrazolium bromide (MTT) was exchanged and cultured for 2 hours. Formazan generated by the opening of the tetrazolium ring was removed. Extraction was performed with 2-propanol, and absorbance at 550 nm was measured with a microplate reader. At the same time, the absorbance at 650 nm was measured as turbidity, and the cell activation effect was evaluated by the difference between the two measured values. The evaluation results are shown in Table 1 as relative values with the cell activation effect in the blank with no sample as 100. In the table, * and ** indicate a significance probability of less than 1% (P <0.05) and a significance probability of less than 1% (P <0.01), respectively, with respect to the significance P value in the t test. This is indicated by *.

Figure 2007246492
Figure 2007246492

表1より明らかなように、フォウクィエリア科植物の抽出物を添加した培地では、有意な真皮線維芽細胞賦活作用が認められた。このことから、フォウクィエリア科植物の抽出物は、優れた細胞賦活作用を有することが明らかとなった。   As is clear from Table 1, a significant dermal fibroblast activation effect was observed in the medium supplemented with the extract of Fauquiliaceae plants. From this, it was clarified that the extract of the Fauqueriaceae plant has an excellent cell activation effect.

次に、フォウクィエリア科植物の抽出物の抗酸化作用について示す。試料には、フォウクィエリア・ミクロフィラの葉を製造例1により抽出したものを試料として評価を行った。   Next, it shows about the antioxidant effect of the extract of Fauquiliaceae plant. The sample was evaluated by extracting the faux quillia microfila leaves according to Production Example 1 as samples.

評価は、以下の手順で行った。50重量%エタノール水溶液にて任意の濃度に希釈したフォウクィエリア科植物の抽出物溶液を96穴マイクロプレートに100μL添加した。次に、0.2mMの濃度になるようにエタノールにて調製した1、1−ジフェニル−2−ピクリルヒドラジル(DPPH)溶液を96穴マイクロプレートに100μL添加した。攪拌しながら暗所に放置し、24時間後に516nmの吸光度を測定した。試料が無添加のブランクの吸光度を(A)、試料を添加したときの吸光度を(B)としたとき、式(1)の値をラジカル消去率とした。評価結果を表2に示した。
式(1) {1−(B)/(A)}×100(%)
The evaluation was performed according to the following procedure. 100 μL of an extract solution of Fauquiliaceae plant diluted to an arbitrary concentration with a 50 wt% ethanol aqueous solution was added to a 96-well microplate. Next, 100 μL of a 1,1-diphenyl-2-picrylhydrazyl (DPPH) solution prepared in ethanol to a concentration of 0.2 mM was added to a 96-well microplate. The mixture was left in the dark with stirring, and the absorbance at 516 nm was measured after 24 hours. When the absorbance of the blank with no sample added was (A) and the absorbance when the sample was added was (B), the value of formula (1) was defined as the radical elimination rate. The evaluation results are shown in Table 2.
Formula (1) {1- (B) / (A)} × 100 (%)

Figure 2007246492
Figure 2007246492

表2より明らかなように、フォウクィエリア科植物の抽出物はラジカル消去に基づく抗酸化作用を有することが分かった。   As is clear from Table 2, it was found that the extract of Fauqueriaceae plant has an antioxidant action based on radical scavenging.

続いて、本発明に係るフォウクィエリア科植物の抽出物を配合した皮膚外用剤の処方例を示す。   Then, the prescription example of the skin external preparation which mix | blended the extract of the Fauquilia family plant based on this invention is shown.

[処方例1]乳液
(1)スクワラン 10.0(重量%)
(2)メチルフェニルポリシロキサン 4.0
(3)水素添加パーム核油 0.5
(4)水素添加大豆リン脂質 0.1
(5)モノステアリン酸ポリオキシエチレン
ソルビタン(20E.O.) 1.3
(6)モノステアリン酸ソルビタン 1.0
(7)グリセリン 4.0
(8)パラオキシ安息香酸メチル 0.1
(9)カルボキシビニルポリマー 0.15
(10)精製水 57.85
(11)アルギニン(1重量%水溶液) 20.0
(12)フォウクィエリア科植物の抽出物[製造例1] 1.0
製法:(1)〜(6)の油相成分を80℃にて加熱溶解する。一方(7)〜(10)の水相成分を80℃にて加熱溶解する。これに前記油相成分を攪拌しながら加え、ホモジナイザーにより均一に乳化する。乳化終了後、冷却を開始し、(11)と(12)を順次加え、均一に混合する。
[Formulation Example 1] Emulsion (1) Squalane 10.0 (wt%)
(2) Methylphenylpolysiloxane 4.0
(3) Hydrogenated palm kernel oil 0.5
(4) Hydrogenated soybean phospholipid 0.1
(5) Polyoxyethylene monostearate
Sorbitan (20E.O.) 1.3
(6) Sorbitan monostearate 1.0
(7) Glycerin 4.0
(8) Methyl paraoxybenzoate 0.1
(9) Carboxyvinyl polymer 0.15
(10) Purified water 57.85
(11) Arginine (1 wt% aqueous solution) 20.0
(12) Fouqui area family plant extract [Production Example 1] 1.0
Production method: The oil phase components (1) to (6) are heated and dissolved at 80 ° C. On the other hand, the aqueous phase components (7) to (10) are dissolved by heating at 80 ° C. The oil phase component is added to this while stirring and uniformly emulsified with a homogenizer. After emulsification, start cooling and add (11) and (12) sequentially and mix uniformly.

[処方例2]化粧水
(1)エタノール 15.0(重量%)
(2)ポリオキシエチレン(40E.O.)硬化ヒマシ油 0.3
(3)香料 0.1
(4)精製水 82.38
(5)クエン酸 0.02
(6)クエン酸ナトリウム 0.1
(7)グリセリン 1.0
(8)ヒドロキシエチルセルロース 0.1
(9)フォウクィエリア科植物の抽出物[製造例3] 1.0
製法:(1)に(2)及び(3)を溶解する。溶解後、(4)〜(8)を順次添加した後、十分に攪拌し、(9)を加え、均一に混合する。
[Prescription Example 2] Lotion (1) Ethanol 15.0 (% by weight)
(2) Polyoxyethylene (40E.O.) hydrogenated castor oil 0.3
(3) Fragrance 0.1
(4) Purified water 82.38
(5) Citric acid 0.02
(6) Sodium citrate 0.1
(7) Glycerin 1.0
(8) Hydroxyethyl cellulose 0.1
(9) Extract of Fouquilliaceae plant [Production Example 3] 1.0
Production method: (2) and (3) are dissolved in (1). After dissolution, (4) to (8) are sequentially added, and then sufficiently stirred, (9) is added and mixed uniformly.

[処方例3]クリーム
(1)スクワラン 10.0(重量%)
(2)ステアリン酸 2.0
(3)水素添加パーム核油 0.5
(4)水素添加大豆リン脂質 0.1
(5)セタノール 3.6
(6)親油型モノステアリン酸グリセリン 2.0
(7)グリセリン 10.0
(8)パラオキシ安息香酸メチル 0.1
(9)アルギニン(20重量%水溶液) 15.0
(10)精製水 40.7
(11)カルボキシビニルポリマー(1重量%水溶液) 15.0
(12)フォウクィエリア科植物の抽出物[製造例1] 1.0
製法:(1)〜(6)の油相成分を80℃にて加熱溶解する。一方(7)〜(10)の水相成分を80℃にて加熱溶解する。これに前記油相成分を攪拌しながら加え、ホモジナイザーにより均一に乳化する。乳化終了後、(11)を加え、冷却を開始し、40℃にて(12)を加え、均一に混合する。
[Prescription Example 3] Cream (1) Squalane 10.0 (% by weight)
(2) Stearic acid 2.0
(3) Hydrogenated palm kernel oil 0.5
(4) Hydrogenated soybean phospholipid 0.1
(5) Cetanol 3.6
(6) Lipophilic glyceryl monostearate 2.0
(7) Glycerin 10.0
(8) Methyl paraoxybenzoate 0.1
(9) Arginine (20% by weight aqueous solution) 15.0
(10) Purified water 40.7
(11) Carboxyvinyl polymer (1% by weight aqueous solution) 15.0
(12) Fouqui area family plant extract [Production Example 1] 1.0
Production method: The oil phase components (1) to (6) are heated and dissolved at 80 ° C. On the other hand, the aqueous phase components (7) to (10) are dissolved by heating at 80 ° C. The oil phase component is added to this while stirring and uniformly emulsified with a homogenizer. After the emulsification is completed, add (11), start cooling, add (12) at 40 ° C., and mix uniformly.

[処方例4]美容液
(1)精製水 27.45(重量%)
(2)グリセリン 14.0
(3)ショ糖脂肪酸エステル 1.3
(4)カルボキシビニルポリマー(1重量%水溶液) 17.5
(5)アルギン酸ナトリウム(1重量%水溶液) 15.0
(6)モノラウリン酸ポリグリセリル 1.0
(7)マカデミアナッツ油脂肪酸フィトステリル 3.0
(8)N-ラウロイル-L-グルタミン酸
ジ(フィトステリル−2−オクチルドデシル) 2.0
(9)硬化パーム油 2.0
(10)スクワラン(オリーブ由来) 1.0
(11)ベヘニルアルコール 0.75
(12)ミツロウ 1.0
(13)ホホバ油 1.0
(14)1、3−ブチレングリコール 10.0
(15)L−アルギニン(10重量%水溶液) 2.0
(16)フォウクィエリア科植物の抽出物[製造例1] 1.0
製法:(1)〜(6)の水相成分を混合し、75℃にて加熱溶解する。一方、(7)〜(14)の油相成分を混合し、75℃にて加熱溶解する。次いで、上記水相成分に油相成分を添加して予備乳化を行った後、ホモミキサーにて均一に乳化する。乳化終了後に冷却を開始し、50℃にて(15)を加える。さらに40℃まで冷却し、(16)を加え、均一に混合する。
[Formulation Example 4] Cosmetic liquid (1) Purified water 27.45 (% by weight)
(2) Glycerol 14.0
(3) Sucrose fatty acid ester 1.3
(4) Carboxyvinyl polymer (1% by weight aqueous solution) 17.5
(5) Sodium alginate (1 wt% aqueous solution) 15.0
(6) Polyglyceryl monolaurate 1.0
(7) Macadamia nut oil fatty acid phytosteryl 3.0
(8) N-lauroyl-L-glutamic acid di (phytosteryl-2-octyldodecyl) 2.0
(9) Hardened palm oil 2.0
(10) Squalane (from olive) 1.0
(11) Behenyl alcohol 0.75
(12) Beeswax 1.0
(13) Jojoba oil 1.0
(14) 1,3-butylene glycol 10.0
(15) L-arginine (10% by weight aqueous solution) 2.0
(16) Extract of Fouquilliaceae plant [Production Example 1] 1.0
Production method: The aqueous phase components (1) to (6) are mixed and dissolved by heating at 75 ° C. On the other hand, the oil phase components (7) to (14) are mixed and dissolved by heating at 75 ° C. Next, the oil phase component is added to the aqueous phase component and preliminary emulsification is performed, followed by uniform emulsification with a homomixer. Cooling is started after completion of emulsification, and (15) is added at 50 ° C. Cool further to 40 ° C, add (16) and mix evenly.

[処方例5]水性ジェル
(1)カルボキシビニルポリマー 0.5(重量%)
(2)精製水 86.7
(3)水酸化ナトリウム(10重量%水溶液) 0.5
(4)エタノール 10.0
(5)パラオキシ安息香酸メチル 0.1
(6)香料 0.1
(7)フォウクィエリア科植物の抽出物[製造例4] 2.0
(8)ポリオキシエチレン(60E.O.)硬化ヒマシ油 0.1
製法:(1)を(2)に加え、均一に攪拌した後、(3)を加える。均一に攪拌した後、(4)に予め溶解した(5)を加える。均一に攪拌した後、予め混合しておいた(6)〜(8)を加え、均一に攪拌混合する。
[Formulation Example 5] Aqueous gel (1) Carboxyvinyl polymer 0.5 (% by weight)
(2) Purified water 86.7
(3) Sodium hydroxide (10% by weight aqueous solution) 0.5
(4) Ethanol 10.0
(5) Methyl paraoxybenzoate 0.1
(6) Fragrance 0.1
(7) Fouqui area family plant extract [Production Example 4] 2.0
(8) Polyoxyethylene (60E.O.) hydrogenated castor oil 0.1
Manufacturing method: (1) is added to (2), and after stirring uniformly, (3) is added. After stirring uniformly, (5) previously dissolved in (4) is added. After stirring uniformly, the previously mixed (6) to (8) are added and stirred and mixed uniformly.

[処方例6]クレンジング料
(1)スクワラン 81.0(重量%)
(2)イソステアリン酸ポリオキシエチレングリセリル 15.0
(3)精製水 3.0
(4)フォウクィエリア科植物の抽出物[製造例4] 1.0
製法:(1)と(2)を均一に溶解する。これに、(3)と(4)を順次加え、均一に混合する。
[Formulation Example 6] Cleansing Fee (1) Squalane 81.0 (wt%)
(2) Polyoxyethylene glyceryl isostearate 15.0
(3) Purified water 3.0
(4) Extract of Fouquilliaceae plant [Production Example 4] 1.0
Manufacturing method: (1) and (2) are uniformly dissolved. (3) and (4) are sequentially added to this and mixed uniformly.

[処方例7]洗顔フォーム
(1)ステアリン酸 16.0(重量%)
(2)ミリスチン酸 16.0
(3)親油型モノステアリン酸グリセリン 2.0
(4)グリセリン 20.0
(5)水酸化ナトリウム 7.5
(6)ヤシ油脂肪酸アミドプロピルベタイン 1.0
(7)精製水 36.5
(8)フォウクィエリア科植物の抽出物[製造例3] 1.0
製法:(1)〜(4)の油相成分を80℃にて加熱溶解する。一方(5)〜(7)の水相成分を80℃にて加熱溶解し、油相成分と均一に混合撹拌する。冷却を開始し、40℃にて(8)を加え、均一に混合する。
[Prescription Example 7] Face-wash foam (1) Stearic acid 16.0 (% by weight)
(2) Myristic acid 16.0
(3) Lipophilic glyceryl monostearate 2.0
(4) Glycerin 20.0
(5) Sodium hydroxide 7.5
(6) Palm oil fatty acid amidopropyl betaine 1.0
(7) Purified water 36.5
(8) Fouqui area family plant extract [Production Example 3] 1.0
Production method: The oil phase components (1) to (4) are heated and dissolved at 80 ° C. On the other hand, the aqueous phase components (5) to (7) are heated and dissolved at 80 ° C., and mixed and stirred uniformly with the oil phase components. Cooling is started, and (8) is added at 40 ° C. and mixed uniformly.

[処方例8]メイクアップベースクリーム
(1)スクワラン 10.0(重量%)
(2)セタノール 2.0
(3)グリセリントリ−2−エチルヘキサン酸エステル 2.5
(4)親油型モノステアリン酸グリセリル 1.0
(5)プロピレングリコール 11.0
(6)ショ糖脂肪酸エステル 1.3
(7)精製水 69.4
(8)酸化チタン 1.0
(9)ベンガラ 0.1
(10)黄酸化鉄 0.4
(11)香料 0.1
(12)フォウクィエリア科植物の抽出物[製造例2] 1.2
製法:(1)〜(4)の油相成分を混合し、75℃にて加熱溶解する。一方、(5)〜(7)の水相成分を混合し、75℃にて加熱溶解し、これに(8)〜(10)の顔料を加え、ホモミキサーにて均一に分散させる。この水相成分に前記油相成分を加え、ホモミキサーにて乳化する。乳化終了後に冷却を開始し、40℃にて(11)と(12)の成分を加え、均一に混合する。
[Prescription Example 8] Make-up base cream (1) Squalane 10.0 (% by weight)
(2) Cetanol 2.0
(3) Glycerin tri-2-ethylhexanoate 2.5
(4) Lipophilic glyceryl monostearate 1.0
(5) Propylene glycol 11.0
(6) Sucrose fatty acid ester 1.3
(7) Purified water 69.4
(8) Titanium oxide 1.0
(9) Bengala 0.1
(10) Yellow iron oxide 0.4
(11) Fragrance 0.1
(12) Extract of Fouquilliaceae plant [Production Example 2] 1.2
Production method: The oil phase components (1) to (4) are mixed and dissolved by heating at 75 ° C. On the other hand, the aqueous phase components (5) to (7) are mixed and dissolved by heating at 75 ° C., and the pigments (8) to (10) are added thereto and dispersed uniformly with a homomixer. The oil phase component is added to the water phase component and emulsified with a homomixer. Cooling is started after the emulsification is completed, and the components (11) and (12) are added at 40 ° C. and mixed uniformly.

[処方例9]乳液状ファンデーション
(1)メチルポリシロキサン 2.0(重量%)
(2)スクワラン 5.0
(3)ミリスチン酸オクチルドデシル 5.0
(4)セタノール 1.0
(5)ポリオキシエチレン(20E.O.)
ソルビタンモノステアリン酸エステル 1.3
(6)モノステアリン酸ソルビタン 0.7
(7)1、3−ブチレングリコール 8.0
(8)キサンタンガム 0.1
(9)パラオキシ安息香酸メチル 0.1
(10)精製水 57.4
(11)酸化チタン 9.0
(12)タルク 7.4
(13)ベンガラ 0.5
(14)黄酸化鉄 1.1
(15)黒酸化鉄 0.1
(16)香料 0.1
(17)フォウクィエリア科植物の抽出物[製造例4] 1.0
製法:(1)〜(6)の油相成分を混合し、75℃にて加熱溶解する。一方、(7)〜(10)の水相成分を混合し、75℃にて加熱溶解し、これに(11)〜(15)の顔料を加え、ホモミキサーにて均一に分散する。油相成分を加え、乳化を行う。乳化終了後に冷却を開始し、40℃にて(16)と(17)の成分を順次加え、均一に混合する。
[Formulation Example 9] Emulsion foundation (1) Methylpolysiloxane 2.0 (wt%)
(2) Squalane 5.0
(3) Octyldodecyl myristate 5.0
(4) Cetanol 1.0
(5) Polyoxyethylene (20E.O.)
Sorbitan monostearate 1.3
(6) Sorbitan monostearate 0.7
(7) 1,3-butylene glycol 8.0
(8) Xanthan gum 0.1
(9) Methyl paraoxybenzoate 0.1
(10) Purified water 57.4
(11) Titanium oxide 9.0
(12) Talc 7.4
(13) Bengala 0.5
(14) Yellow iron oxide 1.1
(15) Black iron oxide 0.1
(16) Fragrance 0.1
(17) Extract from Fouquilliaceae plant [Production Example 4] 1.0
Production method: The oil phase components (1) to (6) are mixed and dissolved by heating at 75 ° C. On the other hand, the aqueous phase components (7) to (10) are mixed and dissolved by heating at 75 ° C., and the pigments (11) to (15) are added thereto and uniformly dispersed with a homomixer. Add oil phase ingredients and emulsify. Cooling is started after the emulsification is completed, and components (16) and (17) are sequentially added at 40 ° C. and mixed uniformly.

[処方例10]油中水型エモリエントクリーム
(1)流動パラフィン 30.0(重量%)
(2)マイクロクリスタリンワックス 2.0
(3)ワセリン 5.0
(4)ジグリセリンオレイン酸エステル 5.0
(5)塩化ナトリウム 1.3
(6)塩化カリウム 0.1
(7)プロピレングリコール 3.0
(8)1、3−ブチレングリコール 5.0
(9)パラオキシ安息香酸メチル 0.1
(10)フォウクィエリア科植物の抽出物[製造例1] 1.0
(11)精製水 47.4
(12)香料 0.1
製法:(5)と(6)を(11)の一部に溶解して50℃とし、50℃に加熱した(4)に撹拌しながら徐々に加える。これを混合した後、70℃にて加熱溶解した(1)〜(3)に均一に分散する。これに(7)〜(10)を(11)の残部に70℃にて加熱溶解したものを撹拌しながら加え、ホモミキサーにて乳化する。乳化終了後に冷却を開始し、40℃にて(12)を加え、均一に混合する。
[Formulation Example 10] Water-in-oil emollient cream (1) Liquid paraffin 30.0 (% by weight)
(2) Microcrystalline wax 2.0
(3) Vaseline 5.0
(4) Diglycerin oleate 5.0
(5) Sodium chloride 1.3
(6) Potassium chloride 0.1
(7) Propylene glycol 3.0
(8) 1,3-butylene glycol 5.0
(9) Methyl paraoxybenzoate 0.1
(10) Fouqui area family plant extract [Production Example 1] 1.0
(11) Purified water 47.4
(12) Fragrance 0.1
Production method: Dissolve (5) and (6) in a part of (11) to 50 ° C., and gradually add to (4) heated to 50 ° C. with stirring. After mixing this, it disperse | distributes uniformly to (1)-(3) heated and melt | dissolved at 70 degreeC. (7) to (10) are added to the remainder of (11) heated and dissolved at 70 ° C. while stirring and emulsified with a homomixer. Cooling is started after completion of emulsification, and (12) is added at 40 ° C. and mixed uniformly.

[処方例11]パック
(1)精製水 62.9(重量%)
(2)ポリビニルアルコール 12.0
(3)エタノール 17.0
(4)グリセリン 5.0
(5)ポリエチレングリコール(平均分子量1000) 2.0
(6)フォウクィエリア科植物の抽出物[製造例2] 1.0
(7)香料 0.1
製法:(2)と(3)を混合し、80℃に加温した後、80℃に加温した(1)に溶解する。均一に溶解した後、(4)と(5)を加え、攪拌しながら冷却を開始する。40℃まで冷却し、(6)と(7)を加え、均一に混合する。
[Prescription Example 11] Pack (1) Purified water 62.9 (% by weight)
(2) Polyvinyl alcohol 12.0
(3) Ethanol 17.0
(4) Glycerin 5.0
(5) Polyethylene glycol (average molecular weight 1000) 2.0
(6) Fouqui area family plant extract [Production Example 2] 1.0
(7) Fragrance 0.1
Production method: (2) and (3) are mixed, heated to 80 ° C, and then dissolved in (1) heated to 80 ° C. After uniformly dissolving, add (4) and (5), and start cooling while stirring. Cool to 40 ° C, add (6) and (7) and mix uniformly.

[処方例12]入浴剤
(1)香料 0.3(重量%)
(2)フォウクィエリア科植物の抽出物[製造例1] 1.0
(3)炭酸水素ナトリウム 50.0
(4)硫酸ナトリウム 48.7
製法:(1)〜(4)を均一に混合する。
[Prescription Example 12] Bath agent (1) Fragrance 0.3 (% by weight)
(2) Fouqui area family plant extract [Production Example 1] 1.0
(3) Sodium bicarbonate 50.0
(4) Sodium sulfate 48.7
Production method: (1) to (4) are mixed uniformly.

[処方例13]ヘアーワックス
(1)ステアリン酸 3.0(重量%)
(2)マイクロクリスタリンワックス 2.0
(3)セチルアルコール 3.0
(4)高重合メチルポリシロキサン 2.0
(5)メチルポリシロキサン 5.0
(6)ポリ(オキシエチレン・オキシプロピレン)
メチルポリシロキサン共重合体 1.0
(7)パラオキシ安息香酸メチル 0.1
(8)1、3−ブチレングリコール 7.5
(9)アルギニン 0.7
(10)精製水 74.6
(11)フォウクィエリア科植物の抽出物[製造例1] 1.0
(12)香料 0.1
製法:(1)〜(6)の油相成分を混合し、75℃にて加熱溶解後する。一方、(7)〜(10)の水相成分を75℃にて加熱溶解し、前記油相成分を加え、ホモミキサーにて乳化する。乳化終了後に冷却を開始し、40℃にて(11)と(12)の成分を加え、均一に混合する。
[Prescription Example 13] Hair wax (1) Stearic acid 3.0 (% by weight)
(2) Microcrystalline wax 2.0
(3) Cetyl alcohol 3.0
(4) Highly polymerized methylpolysiloxane 2.0
(5) Methylpolysiloxane 5.0
(6) Poly (oxyethylene / oxypropylene)
Methylpolysiloxane copolymer 1.0
(7) Methyl paraoxybenzoate 0.1
(8) 1,3-butylene glycol 7.5
(9) Arginine 0.7
(10) Purified water 74.6
(11) Fouqui area family plant extract [Production Example 1] 1.0
(12) Fragrance 0.1
Production method: The oil phase components (1) to (6) are mixed and heated and dissolved at 75 ° C. On the other hand, the aqueous phase components (7) to (10) are dissolved by heating at 75 ° C., the oil phase component is added, and the mixture is emulsified with a homomixer. Cooling is started after the emulsification is completed, and the components (11) and (12) are added at 40 ° C. and mixed uniformly.

[処方例14]ヘアートニック
(1)エタノール 50.0(重量%)
(2)精製水 48.9
(3)フォウクィエリア科植物の抽出物[製造例3] 1.0
(4)香料 0.1
製法:(1)〜(4)の成分を混合、均一化する。
[Prescription Example 14] Hair artic (1) Ethanol 50.0 (% by weight)
(2) Purified water 48.9
(3) Fouqui area family plant extract [Production Example 3] 1.0
(4) Fragrance 0.1
Production method: Components (1) to (4) are mixed and homogenized.

[処方例15]錠剤
(1)フォウクィエリア科植物の抽出物[製造例1] 100.0(mg)
(2)還元麦芽糖水飴 461.0
(3)トウモロコシデンプン 15.0
(4)グリセリン脂肪酸エステル 12.0
(5)香料 12.0
製法:(1)〜(3)をそれぞれ篩過して混合し、次いで、(4)〜(5)を添加して混合した。その後、常法により打錠して、全量が600mgの錠剤を得た。
[Prescription Example 15] Tablet (1) Extract from Fauquilariaceae [Production Example 1] 100.0 (mg)
(2) Reduced maltose starch syrup 461.0
(3) Corn starch 15.0
(4) Glycerin fatty acid ester 12.0
(5) Fragrance 12.0
Production method: (1) to (3) were sieved and mixed, and then (4) to (5) were added and mixed. Thereafter, tableting was performed by a conventional method to obtain a tablet having a total amount of 600 mg.

次に、フォウクィエリア科植物の抽出物を配合した処方を用いて使用試験を行い、乾燥による肌荒れについて改善効果を評価した。その際、処方例1に示した乳液の処方に表3に記載するフォウクィエリア科植物の抽出物をそれぞれ配合し、実施例1〜2として使用試験を行った。また、フォウクィエリア科植物の抽出物を精製水に代替し、比較例1として同時に使用試験を行った。   Next, a use test was conducted using a formulation in which an extract of a fauque area family plant was blended, and an improvement effect was evaluated for rough skin caused by drying. At that time, the extract of Fauquiliaceae plant listed in Table 3 was blended in the emulsion formulation shown in Formulation Example 1, and the use test was conducted as Examples 1-2. Moreover, the extract of the Fauquilia family plant was replaced with purified water, and a use test was simultaneously conducted as Comparative Example 1.

Figure 2007246492
Figure 2007246492

各試料について、肌荒れ症状が顕著に認められる30〜50才代の乾燥肌の女性パネラー20名をそれぞれ一群とし、ブラインドにて1週間使用させ、使用前後の皮膚状態の変化を観察して評価した。皮膚症状の指標として、乾燥による肌荒れについて、「改善」、「やや改善」、「変化なし」の三段階で評価し、表4に各評価を得たパネラー数にて示した。   For each sample, 20 female panelists with dry skin in their 30s to 50s whose skin symptom was remarkably recognized were grouped and used for one week blindly, and the skin condition before and after use was observed and evaluated. . As an index of skin symptoms, rough skin due to dryness was evaluated in three stages of “improvement”, “slight improvement”, and “no change”, and Table 4 shows the number of panelists that obtained each evaluation.

Figure 2007246492
Figure 2007246492

表4より、フォウクィエリア科植物の抽出物を含有しない比較例使用群においては、8割以上のパネラーに改善は認められなかったが、フォウクィエリア科植物の抽出物を配合した実施例使用群においては、7割以上のパネラーに明確な肌荒れの改善が認められた。このことから、フォウクィエリア科植物の抽出物は優れた保湿効果を有することが明らかとなった。


From Table 4, in the comparative example use group that does not contain the extract of the focus area family plant, an improvement was not recognized in more than 80% of the panelists, but the use of the example in which the extract of the focus area family plant was blended In the group, more than 70% of panelists showed a clear improvement in rough skin. From this, it was clarified that the extract of the Fauqueriaceae plant has an excellent moisturizing effect.


Claims (5)

フォウクィエリア科植物より選ばれる1種又は2種以上の植物の抽出物を有効成分とする保湿剤。 A moisturizing agent containing as an active ingredient an extract of one or more kinds of plants selected from Fouquiria family plants. フォウクィエリア科植物より選ばれる1種又は2種以上の植物の抽出物を有効成分とする細胞賦活剤。 A cell activator comprising, as an active ingredient, an extract of one or more kinds of plants selected from Fouqui area family plants. フォウクィエリア科植物より選ばれる1種又は2種以上の植物の抽出物を有効成分とする抗酸化剤。 The antioxidant which uses the extract of 1 type, or 2 or more types of plants chosen from a Fauquilia family plant as an active ingredient. フォウクィエリア科植物より選ばれる1種又は2種以上の植物の抽出物を含有する皮膚外用剤。 A skin external preparation containing an extract of one or two or more kinds of plants selected from the Fauquilia family plants. フォウクィエリア科植物より選ばれる1種又は2種以上の植物の抽出物を含有する食品。

A food containing an extract of one or two or more kinds of plants selected from Fouqui area family plants.

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2945943A1 (en) * 2009-06-01 2010-12-03 Lvmh Rech USE OF A VEGETABLE EXTRACT RICH IN POLYPHENOLS AS ANTIOXIDANT AGENT IN ASSOCIATION WITH A HYDRATING OR HUMICIZING AGENT

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1239313A (en) * 1917-05-31 1917-09-04 Edgar W Snyder Chewing-gum.
JPS6248611A (en) * 1985-08-28 1987-03-03 Shiseido Co Ltd External preparation for skin
US5824312A (en) * 1994-03-10 1998-10-20 Imarx Pharmaceutical Corp. Sunscreen agents from natural sources
JP2004115513A (en) * 2002-09-23 2004-04-15 Merck Patent Gmbh Preparation having antioxidant property

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1239313A (en) * 1917-05-31 1917-09-04 Edgar W Snyder Chewing-gum.
JPS6248611A (en) * 1985-08-28 1987-03-03 Shiseido Co Ltd External preparation for skin
US5824312A (en) * 1994-03-10 1998-10-20 Imarx Pharmaceutical Corp. Sunscreen agents from natural sources
JP2004115513A (en) * 2002-09-23 2004-04-15 Merck Patent Gmbh Preparation having antioxidant property

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2945943A1 (en) * 2009-06-01 2010-12-03 Lvmh Rech USE OF A VEGETABLE EXTRACT RICH IN POLYPHENOLS AS ANTIOXIDANT AGENT IN ASSOCIATION WITH A HYDRATING OR HUMICIZING AGENT
US8168211B2 (en) 2009-06-01 2012-05-01 Lvmh Recherche Use of a polyphenol-rich plant extract as antioxidant in combination with a hydrating or humectant agent

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