JP2006306804A - Wrinkle formation inhibitor - Google Patents
Wrinkle formation inhibitor Download PDFInfo
- Publication number
- JP2006306804A JP2006306804A JP2005132793A JP2005132793A JP2006306804A JP 2006306804 A JP2006306804 A JP 2006306804A JP 2005132793 A JP2005132793 A JP 2005132793A JP 2005132793 A JP2005132793 A JP 2005132793A JP 2006306804 A JP2006306804 A JP 2006306804A
- Authority
- JP
- Japan
- Prior art keywords
- wrinkle formation
- acteoside
- formation inhibitor
- wrinkle
- mass
- 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.)
- Pending
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Classifications
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- 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
- A61Q19/08—Anti-ageing preparations
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
-
- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/60—Sugars; Derivatives thereof
- A61K8/602—Glycosides, e.g. rutin
-
- 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
- A61K8/9728—Fungi, e.g. yeasts
-
- 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
- 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]
- A61K8/9794—Liliopsida [monocotyledons]
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/92—Oral administration
Abstract
Description
本発明は、アクテオシドを有効成分として含有してなるシワ形成抑制剤に関する。 The present invention relates to a wrinkle formation inhibitor comprising acteoside as an active ingredient.
皮膚は生体の最外層にあるため、紫外線の曝露などの環境からの影響を直接受け、種々のトラブルが発生する。中でもシワは加齢による老化と紫外線による老化(光老化)により形成され、美容上大きな問題となっている。特に紫外線により形成されるシワは深く顕著であり、活性酸素種の慢性的な産生やSOD活性の低下などがその形成に関与していると考えられている。 Since the skin is the outermost layer of the living body, it is directly affected by the environment such as exposure to ultraviolet rays, and various troubles occur. Among them, wrinkles are formed by aging due to aging and aging due to ultraviolet rays (photoaging), which is a major cosmetic problem. In particular, wrinkles formed by ultraviolet rays are prominent and prominent, and it is considered that chronic production of reactive oxygen species and a decrease in SOD activity are involved in the formation thereof.
そこでシワの形成を抑制するために、これまで化粧料においては抗酸化剤(特許文献1)、植物抽出物(特許文献2)、レチノイン酸δ−トコフェリル(特許文献3)の利用などが提案されている。一方、経口食品としてはイソフラボン配糖体(特許文献4)やコエンザイムQ10(非特許文献1)の利用が報告されている。しかしながら、これらのシワ形成抑制効果は必ずしも十分に満足のいくものとはいえず、より実効のあるシワ形成抑制素材が求められていた。 Thus, in order to suppress the formation of wrinkles, the use of antioxidants (Patent Document 1), plant extracts (Patent Document 2), retinoic acid δ-tocopheryl (Patent Document 3), etc. has been proposed so far. ing. On the other hand, use of isoflavone glycosides (Patent Document 4) and coenzyme Q 10 (Non-Patent Document 1) has been reported as oral foods. However, these wrinkle formation suppressing effects are not always satisfactory, and a more effective wrinkle formation suppressing material has been demanded.
一方、アクテオシドは植物中に広く含まれる化合物であり、抗酸化作用を有することが報告されている(非特許文献2)。そして、紫外線吸収剤(特許文献5)、5−リポキシゲナーゼ阻害剤(特許文献6)、アレルギー及び成人病予防食品(特許文献7)、退色抑制剤(特許文献8)等として、様々な機能や生理活性が見出されている。 On the other hand, acteoside is a compound widely contained in plants, and has been reported to have an antioxidant effect (Non-patent Document 2). And various functions and physiology as an ultraviolet absorber (patent document 5), 5-lipoxygenase inhibitor (patent document 6), allergy and adult disease prevention food (patent document 7), fading inhibitor (patent document 8), etc. Activity has been found.
斯かる状況下、本発明の目的とするところは、紫外線等の外的要因や老化等の内的要因により形成されるシワを、外用塗布及び/又は内服による手法により、効果的に抑制する
ことが可能なシワ形成抑制剤を提供することにある。
Under such circumstances, the object of the present invention is to effectively suppress wrinkles formed by external factors such as ultraviolet rays and internal factors such as aging by means of external application and / or internal use. It is in providing the wrinkle formation inhibitor which can do.
本発明者らは、上記事情に鑑みて鋭意研究を行った結果、アクテオシドを外用塗布及び/又は経口摂取することで、紫外線照射によるシワ形成が抑制されることを確認し、本発明を完成するに至った。即ち、本願発明は、下式で表されるアクテオシドを有効成分として含有することを特徴とするシワ形成抑制剤にある。
本願第2の発明は、上記シワ形成抑制剤が、オリーブの実を圧搾して得られるベジテーション水、或いはオリーブの実を圧搾して得られる固相部及び/又は水相部であることを特徴とするシワ形成抑制剤にあり、第3の発明は、上記シワ形成抑制剤が、オリーブの実を圧搾して得られる固相部及び/又は水相部より、水及び/又は有機溶媒を用い抽出して得られる抽出物であることを特徴とするシワ形成抑制剤にある。また第4の発明は、上記シワ形成抑制剤におけるアクテオシドの含有量が1.0質量%以上であることを特徴とする上記のシワ形成抑制剤にある。 The second invention of the present application is that the wrinkle formation inhibitor is a vegetation water obtained by squeezing olive fruit, or a solid phase part and / or an aqueous phase part obtained by squeezing olive fruit. According to a third aspect of the present invention, there is provided a wrinkle formation inhibitor, wherein the wrinkle formation inhibitor contains water and / or an organic solvent from a solid phase part and / or an aqueous phase part obtained by pressing olive fruit. A wrinkle formation inhibitor characterized by being an extract obtained by use and extraction. According to a fourth aspect of the present invention, there is provided the aforementioned wrinkle formation inhibitor, wherein the content of acteoside in the wrinkle formation inhibitor is 1.0% by mass or more.
本願第5の発明は、上記シワ形成抑制剤を配合することを特徴とする化粧料であり、当該シワ形成抑制剤の有効成分であるアクテオシドの配合量が、化粧料の総量を基準として、0.001〜2.0質量%であることを特徴とするシワ形成抑制用化粧料にある。また本願第6の発明は、上記シワ形成抑制剤を配合することを特徴とする飲食品組成物であり、当該シワ形成抑制剤の有効成分であるアクテオシドの配合量が、飲食品組成物の総量を基準として、0.001〜10.0質量%であることを特徴とするシワ形成抑制用飲食品組成物にある。さらに本願第7の発明は、上記シワ形成抑制剤の有効成分であるアクテオシドを、1日当り、経口的に0.001〜0.05g摂取させることを特徴とする摂取方法にある。 The fifth invention of the present application is a cosmetic comprising the above-mentioned wrinkle formation inhibitor, and the amount of acteoside as an active ingredient of the wrinkle formation inhibitor is 0 based on the total amount of the cosmetic. It is in the cosmetic for wrinkle formation suppression characterized by being 0.001-2.0 mass%. The sixth invention of the present application is a food / beverage product composition containing the wrinkle formation inhibitor, and the amount of acteoside, which is an active ingredient of the wrinkle formation inhibitor, is the total amount of the food / beverage product composition. The wrinkle formation-inhibiting food / beverage composition, which is 0.001 to 10.0% by mass based on Further, the seventh invention of the present application lies in an ingestion method characterized in that 0.001 to 0.05 g of acteoside, which is an active ingredient of the wrinkle formation inhibitor, is orally administered per day.
本発明のシワ形成抑制剤は、有効成分としてアクテオシドを含有することを特徴とし、紫外線曝露による光老化や加齢による自然老化に伴って発生するシワの形成を抑制することができる。 The wrinkle formation inhibitor of the present invention is characterized by containing acteoside as an active ingredient, and can suppress the formation of wrinkles that occur due to photoaging due to ultraviolet exposure and natural aging due to aging.
本発明のシワ形成抑制剤の有効成分であるアクテオシドは、モクセイ科、シソ科、イワタバコ科、ハマウツボ科、コショウ科等の各種植物に含まれることが知られているが、これら植物由来のものに限定されるものではない。本発明で使用されるアクテオシドは、例えば、前記植物から適当なものを選択し、抽出精製することにより得ることができる。また、一般の市販品を使用しても良い。モクセイ科オリーブ(Olea europaea L.)の果実は、原料として比較的入手し易く、またアクテオシドの収率も良いため、好ましく用いられる。果実としては産地、品種、食用、搾油用を問わず使用できる。また品種としては、特にコラティナ(Coratina)種がアクテオシドの含有率が高いため、特に好ましく用いられる。 Acteoside, which is an active ingredient of the wrinkle formation inhibitor of the present invention, is known to be contained in various plants such as oleaceae, perillaceae, saccharidaceae, lobster, pepper, etc. It is not limited. The acteoside used in the present invention can be obtained, for example, by selecting an appropriate one from the plant and extracting and purifying it. Moreover, you may use a general commercial item. Olea europaea L. fruit is preferably used because it is relatively easy to obtain as a raw material and the yield of acteoside is good. As a fruit, it can be used regardless of origin, variety, food, and oil extraction. As varieties, particularly, the Coratina species are particularly preferably used because of their high acteoside content.
本発明のアクテオシドを有効成分として含有するシワ形成抑制剤としては、特にオリーブの実を圧搾して得られるベジテーション水、或いはオリーブの実を圧搾して得られる固相部及び/又は水相部が好ましく用いられる。オリーブの実を圧搾して得られるベジテーション水は、通常のオリーブの果実からオリーブ油を得る圧搾過程において産する水溶液部である。またオリーブの実を圧搾して得られる固相部及び/又は水相部における固相部とは、オリーブの実の圧搾物において分離する液相以外の、固形分である圧搾残渣を含む沈澱部分であり、その一部として液相も含まれている。また水相部とは、液相部から、例えば遠心分離等の処理を経て、オリーブ油である油相を除いた後の残りの部分である。 The wrinkle formation inhibitor containing the acteoside of the present invention as an active ingredient is, in particular, vegetation water obtained by squeezing olive fruit, or a solid phase part and / or an aqueous phase part obtained by squeezing olive fruit. Is preferably used. Vegitation water obtained by squeezing olive fruits is an aqueous solution part produced in the squeezing process of obtaining olive oil from ordinary olive fruits. Moreover, the solid phase part obtained by squeezing olive fruit and / or the solid phase part in the aqueous phase part is a precipitated part containing a pressed residue which is a solid content other than the liquid phase separated in the compressed product of olive fruit. And a liquid phase is also included as part of it. The aqueous phase portion is the remaining portion after removing the oil phase, which is olive oil, from the liquid phase portion through a process such as centrifugation.
これらベジテーション水、或いは固相部及び/又は水相部は、そのまま使用することも可能であるが、通常は混入する脂質成分、繊維質成分や種子殻等を濾過や遠心分離を行うことにより除去、精製して用いることが好ましい。また、雑菌の混入による異臭の発生等を抑える目的で、ベジテーション水、或いは固相部及び/又は水相部にアルコール類を添加した後に、濾過や遠心分離を行うことも可能である。ここで用いられるアルコール類としては、エチルアルコール、イソプロピルアルコール、1,3−ブチレングリコール、プロピレングリコール等の親水性のアルコール類や多価アルコールが挙げられ、総量中に好ましくは5〜80質量%、特に好ましくは10〜40質量%の量になるように添加することが好ましい。 These vegetation water, or the solid phase part and / or the aqueous phase part can be used as they are, but usually by filtering or centrifuging the lipid component, fiber component, seed shell, etc. to be mixed. It is preferable to use after removing and purifying. In addition, for the purpose of suppressing the generation of off-flavors due to contamination with germs, it is possible to perform filtration or centrifugation after adding alcohols to the vegetation water or the solid phase and / or the aqueous phase. Examples of the alcohols used here include hydrophilic alcohols such as ethyl alcohol, isopropyl alcohol, 1,3-butylene glycol, and propylene glycol, and polyhydric alcohols. The total amount is preferably 5 to 80% by mass, It is particularly preferable to add so that the amount is 10 to 40% by mass.
さらに本発明においては、有効成分であるアクテオシドを効率的に回収するため、オリーブの実を圧搾して得られる固相部及び/又は水相部より、水及び/又は有機溶媒を用いて抽出し、その抽出物を用いることが好ましい。使用される水及び又は有機溶媒としては、水、エチルアルコール、イソプロピルアルコール、1,3−ブチレングリコール、プロピレングリコール等の親水性のアルコール類や多価アルコール、又はこれらの混液を挙げることができる。 Furthermore, in the present invention, in order to efficiently recover the active ingredient acteoside, extraction is performed using water and / or an organic solvent from the solid phase part and / or the aqueous phase part obtained by pressing olive fruit. It is preferable to use the extract. Examples of the water and / or organic solvent used include water, hydrophilic alcohols such as ethyl alcohol, isopropyl alcohol, 1,3-butylene glycol, and propylene glycol, polyhydric alcohols, and mixtures thereof.
上記のベジテーション水、固相部及び/又は水相部、抽出物は、必要に応じて、濃縮、乾固等させて用いることができる。さらに、これらにおけるアクテオシドの含有率を高めるために、公知の各種精製手段にて精製することも可能である。本発明のシワ形成抑制剤の有効成分であるアクテオシドの含有量は、シワ形成抑制剤に対し1.0質量%以上であることが好ましい。アクテオシドの含有量が1.0質量%以上だと、本発明の目的とするシワ形成抑制効果が十分に発揮され、かつシワ形成抑制剤を機能成分として各種化粧料や飲食品組成物に適用する際に、配合の自由度を十分に確保することが可能となる。 The above-mentioned vegetation water, the solid phase part and / or the aqueous phase part, and the extract can be used after being concentrated, dried or solidified, if necessary. Furthermore, in order to increase the content of acteoside in these, it is also possible to purify by various known purification means. The content of acteoside which is an active ingredient of the wrinkle formation inhibitor of the present invention is preferably 1.0% by mass or more based on the wrinkle formation inhibitor. When the content of acteoside is 1.0% by mass or more, the wrinkle formation inhibitory effect of the present invention is sufficiently exerted, and the wrinkle formation inhibitor is used as a functional ingredient in various cosmetics and food and beverage compositions. At this time, it becomes possible to ensure a sufficient degree of freedom in blending.
本発明のシワ形成抑制剤は、一般の各種化粧料に機能成分として配合することにより、これら化粧料にシワ形成抑制機能を付与することが可能となる。化粧料としては、一般に皮膚に塗布する形の化粧料の他、入浴剤として用いてもよい。剤型としては、一般に用いられる、水溶液、W/O型又はO/W型エマルション、適当な賦形剤等を用いて顆粒剤その他の粉末、錠剤等とすることが考えられ、具体的にはクリーム、乳液、化粧水、パック、ジェル、スティック、シート、パップ等が挙げられるが、これらに限定されるものではない。化粧料に対するシワ形成抑制剤の配合量は、その剤型により適宜選択されるべきものであり一概に規定することはできないが、一般には化粧料の総量に対し、本発明のシワ形成抑制剤を、その有効成分であるアクテオシドとして0.001〜2.0質量%となるように配合するのが好ましく、特に好ましくは0.001〜1.0質量%である。配合量が0.001質量%未満では、シワ形成抑制効果が十分に得られない場合があり、2.0質量%を超えても、その増加分に見合った効果の向上は望めない場合があり、使用時の官能が悪くなる問題、特ににおいが強くなりすぎる問題が生じ易く、個々の剤型を保持し難くなる場合がある。 The wrinkle formation inhibitor of the present invention can be imparted with a wrinkle formation inhibitory function to these cosmetics by being blended as a functional ingredient in various general cosmetics. As cosmetics, in addition to cosmetics generally applied to the skin, they may be used as bathing agents. As the dosage form, it is possible to use a commonly used aqueous solution, W / O type or O / W type emulsion, appropriate excipients, etc. to form granules or other powders, tablets, etc., specifically Examples include, but are not limited to, creams, emulsions, lotions, packs, gels, sticks, sheets, and pops. The blending amount of the wrinkle formation inhibitor with respect to the cosmetics should be appropriately selected according to the dosage form and cannot be specified unconditionally. However, in general, the wrinkle formation inhibitor of the present invention is used with respect to the total amount of the cosmetics. The acteoside, which is the active ingredient, is preferably blended in an amount of 0.001 to 2.0% by mass, particularly preferably 0.001 to 1.0% by mass. If the blending amount is less than 0.001% by mass, the effect of suppressing the formation of wrinkles may not be sufficiently obtained, and if it exceeds 2.0% by mass, the improvement corresponding to the increase may not be expected. The problem that the sensory sensation at the time of use deteriorates, particularly the problem that the smell becomes too strong is likely to occur, and it may be difficult to maintain individual dosage forms.
本発明のシワ形成抑制剤を化粧料に適用する際には、必要に応じて、本願発明の効果を損なわない範囲で、一般に化粧料に適用可能な各種の成分、例えば、タール系色素、酸化鉄等の着色顔料、パラベン等の防腐剤、脂肪酸セッケン、セチル硫酸ナトリウム等の陰イオン性界面活性剤、ポリオキシエチレンアルキルエーテル、ポリオキシエチレン脂肪酸エステル、ポリオキシエチレン多価アルコール脂肪酸エステル、ポリオキシエチレン硬化ヒマシ油、多価アルコール脂肪酸エステル、ポリグリセリン脂肪酸エステル等の非イオン性界面活性剤、テトラアルキルアンモニウム塩等の陽イオン性界面活性剤、ベタイン型、スルホベタイン型、スルホアミノ酸型、N−ステアロイル−L−グルタミン酸ナトリウム等の両イオン性界面活性剤、レシチン、リゾフォスファチジルコリン等の天然系界面活性剤、ゼラチン、カゼイン、デンプン、アラビアガム、カラヤガム、グアガム、ローカストビーンガム、ドラガカントガム、クインスシード、ペクチン、カラギーナン、アルギン酸ソーダ等の天然高分子、メチルセルロース、ヒドロキシエチルセルロース、ヒドロキシプロピルセルロース、カルボキシメチルセルロースナトリウム、エチルセルロース等の半合成高分子、ポリビニルアルコール、ポリビニルメチルエーテル及びコーポリマー、ポリビニルピロリドン、ポリアクリル酸ソーダ、カルボキシビニルポリマー、ポリエチレンオキシドポリマー等の合成高分子、キサンテンガム等の増粘剤、酸化チタン等の顔料、ジブチルヒドロキシトルエン等の抗酸化剤等を適宜配合することができる。 When applying the wrinkle formation inhibitor of the present invention to cosmetics, various components that are generally applicable to cosmetics, such as tar dyes, oxidation, and the like, as long as they do not impair the effects of the present invention. Color pigments such as iron, preservatives such as parabens, fatty acid soaps, anionic surfactants such as sodium cetyl sulfate, polyoxyethylene alkyl ethers, polyoxyethylene fatty acid esters, polyoxyethylene polyhydric alcohol fatty acid esters, polyoxy Nonionic surfactants such as ethylene hydrogenated castor oil, polyhydric alcohol fatty acid ester, polyglycerin fatty acid ester, cationic surfactants such as tetraalkylammonium salt, betaine type, sulfobetaine type, sulfoamino acid type, N- Zwitterionic surfactants such as stearoyl-L-glutamate sodium, , Natural surfactants such as lysophosphatidylcholine, gelatin, casein, starch, gum arabic, karaya gum, guar gum, locust bean gum, dragacanto gum, quince seed, pectin, carrageenan, sodium alginate, methylcellulose , Semi-synthetic polymers such as hydroxyethyl cellulose, hydroxypropyl cellulose, sodium carboxymethyl cellulose, ethyl cellulose, synthetic polymers such as polyvinyl alcohol, polyvinyl methyl ether and copolymer, polyvinyl pyrrolidone, sodium polyacrylate, carboxyvinyl polymer, polyethylene oxide polymer , Thickeners such as xanthene gum, pigments such as titanium oxide, antioxidants such as dibutylhydroxytoluene, etc. That.
また本発明のシワ形成抑制剤は、一般の各種飲食品組成物に機能成分として配合することにより、これら飲食品組成物にシワ形成抑制機能を付与することが可能となる。飲食品組成物としては、経口摂取に適した任意の剤型のものが可能であり、例えば、錠剤、顆粒剤、各種カプセル剤、ドリンク製剤、固形剤等が挙げられる。飲食物としては、飲料、ゼリー、チューインガム、キャンディ、錠菓等が挙げられるが、これらに限定されるものではない。飲食品組成物に対するシワ形成抑制剤の配合量は、その剤型により適宜選択されるべきものであり一概に規定することはできないが、一般には飲食品組成物の総量に対し、本願シワ形成抑制剤を、その有効成分であるアクテオシドとして0.001〜10.0質量%ととなるように配合するのが好ましく、特に好ましくは0.001〜5.0質量%である。配合量が0.001質量%未満では、シワ形成抑制効果を発揮するのに必要なアクテオシドを摂取するのが実質的に難しくなる。また10.0質量%を超えても、それに見合った効果が得られるとは限らず、必要以上に飲食品組成物を過剰摂取した場合には健康上好ましくない影響を与えるおそれもある。 Moreover, the wrinkle formation inhibitor of this invention can provide a wrinkle formation inhibitory function to these food / beverage products compositions by mix | blending as a functional component with various general food / beverage products compositions. The food / beverage composition can be in any dosage form suitable for oral intake, and examples thereof include tablets, granules, various capsules, drink preparations, solid preparations and the like. Examples of the food and drink include, but are not limited to, beverages, jelly, chewing gum, candy, and tablet confectionery. The blending amount of the wrinkle formation inhibitor with respect to the food / beverage composition should be appropriately selected depending on the dosage form and cannot be specified unconditionally. The agent is preferably blended so as to be 0.001 to 10.0% by mass, particularly preferably 0.001 to 5.0% by mass, as the active ingredient, acteoside. If the blending amount is less than 0.001% by mass, it is substantially difficult to ingest acteoside necessary for exerting the effect of suppressing wrinkle formation. Moreover, even if it exceeds 10.0 mass%, the effect commensurate with it is not necessarily acquired, and when an excessive intake of the food / beverage product composition is more than necessary, there is a possibility of having an unfavorable effect on health.
本発明のシワ形成抑制剤を飲食品組成物に適用する際には、必要に応じて、本願発明の効果を損なわない範囲で、一般に飲食品に適用可能な各種の有効成分、例えばビタミンC、ビタミンE、ビタミンB2、ビタミンB6、ニコチン酸アミド等のビタミン類、マグネシウム、亜鉛、クロム等のミネラル類、バナバ、ギムネマ、アロエ、ラカンカ、マコモ、クワの葉、ビワの葉、荷葉、サラシア、紅景天、難消化性デキストリン、石蓮花、茶ポリフェノール、テアニン、ヒスチジン、高麗ニンジン、海藻、ホップ、カイアポイモ、ビール酵母等を配合すると、より効果的である。また、乳化剤、分散剤、懸濁剤、展着剤、浸透剤、湿潤剤、安定剤等を組み合わせて配合することもできる。 When applying the wrinkle formation inhibitor of the present invention to a food / beverage product composition, various active ingredients generally applicable to food / beverage products, such as vitamin C, as long as they do not impair the effects of the present invention. Vitamins such as Vitamin E, Vitamin B2, Vitamin B6, Nicotinamide, Minerals such as Magnesium, Zinc, Chromium, Banaba, Gymnema, Aloe, Lacanca, Macomo, Mulberry Leaves, Loquat Leaves, Cargo Leaves, Salacia, Red It is more effective to add geiten, indigestible dextrin, stone lotus, tea polyphenol, theanine, histidine, ginseng, seaweed, hops, caiapoimo, brewer's yeast and the like. Moreover, an emulsifier, a dispersing agent, a suspending agent, a spreading agent, a penetrating agent, a wetting agent, a stabilizer and the like can be combined.
本発明のシワ形成抑制剤は、適当量を日常的に経口摂取させることにより、その目的である、シワ形成抑制作用を効果的に発揮させることが可能となる。好ましいシワ形成抑制剤の摂取方法としては、成人で1日当り、アクテオシドとして0.001〜0.05g、特に好ましくは0.001〜0.01gとなるように、1〜3回に分けて摂取させる方法が挙げられる。1日の摂取量が0.001g未満ではシワ形成抑制効果が不十分な場合があり、また0.05gを超えてもそれに見合った効果が得られるとは限らない。 The wrinkle formation inhibitor of the present invention can effectively exert the wrinkle formation inhibitory effect, which is its purpose, by ingesting an appropriate amount orally on a daily basis. As a preferred method of ingesting wrinkle formation inhibitors, it is divided into 1 to 3 times so that it is 0.001 to 0.05 g, particularly preferably 0.001 to 0.01 g as acteoside per day for adults. A method is mentioned. If the daily intake is less than 0.001 g, the wrinkle formation inhibitory effect may be insufficient, and even if it exceeds 0.05 g, an effect commensurate with it may not be obtained.
以下、実施例に基づいて本願発明を詳述するが、本願発明がこれら実施例に限定されるわけではない。 EXAMPLES Hereinafter, although this invention is explained in full detail based on an Example, this invention is not necessarily limited to these Examples.
実施例1(アクテオシド粗精製品の製造)
コラティナ種のオリーブ果実2kgを圧搾し、常法に従って固相部と水相部を回収した。回収した固相部及び水相部に含水エタノールを加え、2回抽出した。得られた抽出液を常法にて濃縮乾固させ、アクテオシド含有率が5.0質量%の「アクテオシド粗精製品」を得た。
Example 1 (Production of Acteoside Crude Product)
2 kg of colatina olive fruit was squeezed, and a solid phase part and an aqueous phase part were recovered according to a conventional method. Hydrous ethanol was added to the recovered solid phase part and aqueous phase part and extracted twice. The obtained extract was concentrated and dried by a conventional method to obtain an “acteoside crude product” having an acteoside content of 5.0% by mass.
実施例2(アクテオシド精製品の製造)
実施例1で得たアクテオシド粗精製品250gをメタノールで抽出し、抽出液から溶媒を減圧下にて除去し、メタノール抽出物210gを得た。次にスチレン系合成吸着剤(アンバーライトXAD1180、オルガノ株式会社製)を充填したカラムに、上記メタノール抽出物を精製水に再溶解させた水溶液14.4Lを通液し、精製水で洗浄後、濃度を段階的に変化させたメタノール水溶液を用い順次溶出した。50質量%メタノール水溶液溶出画分から減圧下溶媒を除去した後、凍結乾燥し、アクテオシド含有率が34.0質量%の「アクテオシド精製品」を得た。
Example 2 (Production of purified acteoside product)
250 g of crude acteoside product obtained in Example 1 was extracted with methanol, and the solvent was removed from the extract under reduced pressure to obtain 210 g of a methanol extract. Next, 14.4 L of an aqueous solution in which the methanol extract was re-dissolved in purified water was passed through a column packed with a styrene synthetic adsorbent (Amberlite XAD1180, manufactured by Organo Corporation), washed with purified water, Elution was carried out sequentially using an aqueous methanol solution whose concentration was changed stepwise. After removing the solvent under reduced pressure from the fraction eluted with 50% by mass methanol aqueous solution, the solution was freeze-dried to obtain an “acteoside purified product” having an acteoside content of 34.0% by mass.
実施例3、4、比較例1(外用塗布によるシワ形成抑制試験)
本発明のシワ形成抑制剤の有効成分であるアクテオシドの、外用塗布によるシワ形成抑制効果を、次の光老化モデルを用いた試験により調べた。
Examples 3 and 4, Comparative Example 1 (wrinkle formation suppression test by external application)
The effect of suppressing wrinkle formation by external application of acteoside, which is an active ingredient of the wrinkle formation inhibitor of the present invention, was examined by a test using the following photoaging model.
(試験方法)
1.試験動物
試験開始時10週齢のへアレスマウス1群8匹を用いた。
(Test method)
1. Test animals One group of 8 hairless mice aged 10 weeks at the start of the test was used.
2.シワ形成抑制試験
2−1.光老化条件
光老化は、UVAとUVBそれぞれを、1日1回、週5回の頻度で、ヘアレスマウス背部に4週間連続で照射することにより誘発させた。照射量は、UVAが20J/cm2、25J/cm2、30J/cm2、UVBが20mJ/cm2、30mJ/cm2、40mJ/cm2と、1週毎に段階的に照射量を増量し、3週目以降はそれぞれの最大照射量で照射した。
2. 2. Wrinkle formation inhibition test 2-1. Photoaging conditions Photoaging was induced by irradiating the back of hairless mice with UVA and UVB, once a day, 5 times a week for 4 consecutive weeks. Irradiation dose, UVA has a 20J / cm 2, 25J / cm 2, 30J / cm 2, UVB is 20mJ / cm 2, 30mJ / cm 2, 40mJ / cm 2, escalated the dose every week And after the 3rd week, it irradiated with each maximum irradiation amount.
2−2.評価方法
シワ抑制効果は真皮コラーゲン含有量と表皮厚の変化により評価した。
真皮コラ−ゲン量:全層皮膚を採取してポリトロンホモジナイザー(KINEMATICA社製)で破砕後、コラーゲン画分を抽出して酸加水分解し、ヒドロキシプロリン含有量をアミノ酸分析装置(日本分光製)を用いて定量した。1cm2当たりのヒドロキシプロリン量を真皮コラーゲン含有量の相対的指標とした。
表皮厚:全層皮膚を採取して常法に従って皮膚切片標本を作製したのちヘマトキシリン・エオシン染色を施し、表皮の厚さを画像解析ソフト(マイクロアナライザー、日本ポラデジタル社製)で測定した。
2-2. Evaluation method The wrinkle suppression effect was evaluated by changes in the dermis collagen content and skin thickness.
Dermal collagen amount: The whole skin is collected and crushed with a Polytron homogenizer (KINEMATICA), then the collagen fraction is extracted and acid hydrolyzed, and the hydroxyproline content is determined using an amino acid analyzer (manufactured by JASCO). And quantified. The amount of hydroxyproline per cm 2 was used as a relative index of dermis collagen content.
Epidermis thickness: The skin of all layers was collected and a skin section sample was prepared according to a conventional method, followed by hematoxylin and eosin staining, and the thickness of the epidermis was measured with image analysis software (Microanalyzer, manufactured by Pola Digital Japan).
2−3.試料と試験手順
50質量%エタノール水溶液を基剤(比較例1)として、アクテオシド(ChromaDex社製)を0.5質量%配合した試料と実施例1のアクテオシド粗精製品を10質量%配合した試料を調製し、試験動物に塗布した(実施例3、4)。塗布はUV照射と同じ頻度で行い、1日1回UV照射終了後に、試料0.1mLをヘアレスマウス背部皮膚(直径約2.5cm)に塗布した。最終塗布終了後、屠殺して皮膚を採取し、真皮コラーゲン含有量(1cm2当たりのヒドロキシプロリン量)及び表皮厚を測定し、比較例1の基剤塗布群を対照として、その差を比較した。
2-3. Sample and Test Procedure Using 50% by mass ethanol aqueous solution as a base (Comparative Example 1), a sample containing 0.5% by mass of Acteoside (manufactured by ChromaDex) and a sample containing 10% by mass of Acteoside crude purified product of Example 1 Was prepared and applied to test animals (Examples 3 and 4). Application was performed at the same frequency as UV irradiation, and once UV irradiation was completed once a day, 0.1 mL of the sample was applied to the back skin of hairless mice (diameter: about 2.5 cm). After finishing the final application, the skin was collected by slaughter, and the dermis collagen content (hydroxyproline amount per 1 cm 2 ) and epidermis thickness were measured, and the difference was compared using the base application group of Comparative Example 1 as a control. .
(結果)
本発明のシワ形成抑制剤のマウスの紫外線誘発シワ形成に及ぼす効果を、シワ形成に重要な役割をもつ真皮コラーゲン含有量および表皮厚を指標として評価した結果を表1、2に示す。
(result)
Tables 1 and 2 show the results of evaluating the effect of the wrinkle formation inhibitor of the present invention on ultraviolet ray-induced wrinkle formation in mice using the dermis collagen content and skin thickness, which have an important role in wrinkle formation, as indices.
[表1](真皮コラーゲン含有量)
――――――――――――――――――――――――――――――――
被験試料 濃度 ヒドロキシプロリン量a)
(質量%) (μmol/cm2)
――――――――――――――――――――――――――――――――
実施例3 アクテオシド 0.5 4.98±0.35b)
実施例4 アクテオシド粗精製品 10.0 4.96±0.34b)
比較例1 −(基剤のみ) − 3.85±0.44
――――――――――――――――――――――――――――――――
a)数値は平均値±標準誤差、b)p<0.05(比較例1との有意差)
[Table 1] (Dermal collagen content)
――――――――――――――――――――――――――――――――
Sample concentration Concentration of hydroxyproline a)
(Mass%) (μmol / cm 2 )
――――――――――――――――――――――――――――――――
Example 3 Acteoside 0.5 4.98 ± 0.35 b)
Example 4 Acteoside Crude Product 10.0 4.96 ± 0.34 b)
Comparative Example 1-(Base only)-3.85 ± 0.44
――――――――――――――――――――――――――――――――
a) Values are mean values ± standard error, b) p <0.05 (significant difference from Comparative Example 1)
実施例3、4のアクテオシド及びアクテオシド粗精製品塗布群は、基剤のみの比較例1と比較して、有意に高いコラーゲン含有量(ヒドロキシプロリン量)を示し、光老化により減少する真皮コラーゲン量に対し、アクテオシドが有効であることを示した。 The actineoside and acteoside crude product application groups of Examples 3 and 4 showed significantly higher collagen content (hydroxyproline amount) than that of Comparative Example 1 with only the base, and the amount of dermal collagen decreased by photoaging. In contrast, acteoside was shown to be effective.
[表2](表皮厚)
―――――――――――――――――――――――――――――――――
被験試料 濃度 表皮厚c)
(質量%) (μm)
―――――――――――――――――――――――――――――――――
実施例3 アクテオシド 0.5 45.02±1.56d)
実施例4 アクテオシド粗精製品 10.0 46.03±1.66d)
比較例1 −(基剤のみ) − 55.27±2.52
―――――――――――――――――――――――――――――――――
c)数値は平均値±標準誤差、d)p<0.01(比較例1との有意差)
[Table 2] (Skin thickness)
―――――――――――――――――――――――――――――――――
Test sample concentration Skin thickness c)
(Mass%) (μm)
―――――――――――――――――――――――――――――――――
Example 3 Acteoside 0.5 45.02 ± 1.56 d)
Example 4 Acteoside Crude Product 10.0 46.03 ± 1.66 d)
Comparative Example 1-(Base only)-55.27 ± 2.52
―――――――――――――――――――――――――――――――――
c) Numerical values are mean ± standard error, d) p <0.01 (significant difference from Comparative Example 1)
実施例3、4のアクテオシド及びアクテオシド粗精製品塗布群は、基剤のみの比較例1と比較して、有意に低い表皮厚の数値を示し、光老化により肥厚する表皮厚に対し、アクテオシドが有効であることを示した。 In the groups of Acteoside and Acteoside crude product application of Examples 3 and 4, the value of the skin thickness is significantly lower than that of Comparative Example 1 with only the base, and the Acteoside has a thickness that is thickened by photoaging. It was shown to be effective.
本試験の結果からアクテオシドが、比較例1と比較して明らかに、光老化により減少するコラーゲン量を有意に増加させると共に、表皮厚の肥厚も抑制することから、シワ形成を抑制する効果を有すると考えられた。 From the results of this test, Acteoside clearly has an effect of suppressing wrinkle formation because it significantly increases the amount of collagen decreased by photoaging and also suppresses thickening of the epidermis. It was thought to be.
実施例5、6、比較例2(経口シワ形成抑制試験)
本発明のシワ形成抑制剤の有効成分であるアクテオシドの経口シワ形成抑制効果を、次の光老化モデルを用いた試験により調べた。
Examples 5 and 6, Comparative Example 2 (oral wrinkle formation inhibition test)
The oral wrinkle formation inhibitory effect of acteoside, which is an active ingredient of the wrinkle formation inhibitor of the present invention, was examined by a test using the following photoaging model.
(試験方法)
1.試験動物
試験開始時10週齢のへアレスマウス1群9匹を用いた。
(Test method)
1. Test animals One group of 9 hairless mice 10 weeks of age at the start of the test was used.
2.シワ形成抑制試験
2−1.光老化条件及び評価方法
光老化は、前記の「外用塗布によるシワ形成抑制試験」と同じ条件でUV照射することにより誘発させた。但し照射期間は12週間とした。シワ抑制効果はシワスコアにより評価した。シワスコアは、Bissettらの方法(Photochem. Photobiol.,46:367-378, 1987)に従って採点した。即ち、シワの大きさ及び深さを総合した肉眼判定で、最高点を3点として、「大きく深いシワが観察できる」を3点、「シワが確認できる」を2点、「シワが確認できない」を1点、「正常なキメが観察できる」を0点と採点した。
2. 2. Wrinkle formation inhibition test 2-1. Photoaging conditions and evaluation method Photoaging was induced by UV irradiation under the same conditions as in the “wrinkle formation inhibition test by external application” described above. However, the irradiation period was 12 weeks. The wrinkle suppression effect was evaluated by the wrinkle score. The wrinkle score was scored according to the method of Bissett et al. (Photochem. Photobiol., 46: 367-378, 1987). That is, with the naked eye judgment that combines the size and depth of the wrinkles, the highest point is 3 points, 3 points can be observed for large and deep wrinkles, 2 points can be confirmed for wrinkles, and wrinkles cannot be confirmed. Was scored as 1 point, and “normal texture can be observed” as 0 point.
2−2.試料と試験手順
被験試料として、アクテオシド(ChromaDex社製)、実施例2のアクテオシド精製品を用い、0.5質量%カルボキシメチルセルロース水溶液を基剤(比較例2)として、被験試料を基剤に分散させて試験動物に投与した(実施例5、6)。UV照射開始後5週目から投与を開始し、各照射日のUV照射開始前に、各試験動物に表3に示す投与量になるように、ゾンデで直接胃の中に試料を投与した。尚、各群における投与容量が同じになるように、各被験試料の濃度を適宜調整した。そして、最終照射終了3日後にシワスコアを採点し、比較例2の基剤投与群を対照として、その差を比較した。
2-2. Sample and test procedure As test sample, Acteoside (manufactured by ChromaDex), Acteoside purified product of Example 2 was used, 0.5% by mass carboxymethylcellulose aqueous solution was used as a base (Comparative Example 2), and the test sample was dispersed in the base And administered to test animals (Examples 5 and 6). The administration was started from the 5th week after the start of UV irradiation, and the sample was administered directly into the stomach with a sonde so that the dose shown in Table 3 was given to each test animal before the start of UV irradiation on each irradiation day. The concentration of each test sample was adjusted as appropriate so that the administration volume in each group was the same. And the wrinkle score was scored 3 days after the end of the final irradiation, and the difference was compared using the base administration group of Comparative Example 2 as a control.
(結果)
本発明のシワ形成抑制剤のマウスの紫外線誘発シワ形成に及ぼす効果を、シワスコアを指標として評価した結果を表3に示す。
(result)
Table 3 shows the results of evaluating the effect of the wrinkle formation inhibitor of the present invention on UV-induced wrinkle formation in mice using the wrinkle score as an index.
[表3](シワスコア)
―――――――――――――――――――――――――――――――――
被験試料 投与量 シワスコアe)
(mg/kg)
―――――――――――――――――――――――――――――――――
実施例5 アクテオシド 2.10 1.80±0.30
8.50 1.50±0.25f)
実施例6 アクテオシド精製品 6.25 1.75±0.32
25.0 1.60±0.28f)
比較例2 −(基剤のみ) − 2.65±0.18
―――――――――――――――――――――――――――――――――
e)数値は平均値±標準誤差、f)p<0.05(比較例2との有意差)
[Table 3] (wrinkle score)
―――――――――――――――――――――――――――――――――
Test sample Dose wrinkle score e)
(Mg / kg)
―――――――――――――――――――――――――――――――――
Example 5 Acteoside 2.10 1.80 ± 0.30
8.50 1.50 ± 0.25 f)
Example 6 Acteoside purified product 6.25 1.75 ± 0.32
25.0 1.60 ± 0.28 f)
Comparative Example 2-(Base only)-2.65 ± 0.18
―――――――――――――――――――――――――――――――――
e) Numerical values are mean ± standard error, f) p <0.05 (significant difference from Comparative Example 2)
実施例5及び6におけるアクテオシド及びアクテオシド精製品の低用量投与群は、比較例2の基剤投与群と比較し、紫外線照射により誘発されるシワ形成を抑制する傾向があることがわかった。さらに、高用量投与群では、どちらも有意にシワ形成を抑制することがわかった。 The low dose administration group of acteoside and acteoside purified product in Examples 5 and 6 was found to have a tendency to suppress wrinkle formation induced by ultraviolet irradiation as compared with the base administration group of Comparative Example 2. Furthermore, it was found that both the wrinkle formations were significantly suppressed in the high dose administration group.
尚、本試験においては、経口投与の失敗等による体重減少は認められず、正常な成長曲線が得られた。従って、本試験結果が単に体調不良等によるものでないことも明らかとなった。 In this test, weight loss due to failure of oral administration or the like was not observed, and a normal growth curve was obtained. Therefore, it became clear that this test result was not simply due to poor physical condition.
本発明のシワ形成抑制剤は、以下の例に示すように、各種製剤として提供することができるが、これらに限定されるものではない。尚、配合量の%は全て質量%である。 The wrinkle formation inhibitor of the present invention can be provided as various preparations as shown in the following examples, but is not limited thereto. In addition,% of a compounding quantity is all the mass%.
実施例7(スキンローション)
B成分をC成分中に、均一に溶解した後、A成分とC成分を均一に混合攪拌、分散し次いで容器に充填し、スキンローションを調製した。
配合成分 配合量(%)
−−−−−−−−−−−−−−−−−−−−−−−
(A)
エタノール 10.0
モノラウリン酸 5.0
ポリオキシエチレン(20)ソルビタン
ジブチルヒドロキシトルエン 0.01
香料 0.05
(B)
実施例1のアクテオシド粗精製品 0.5
(C)
グリセリン 5.0
キサンタンガム 0.1
ヒドロキシエチルセルロース 0.1
精製水 残 量
Example 7 (skin lotion)
After the B component was uniformly dissolved in the C component, the A component and the C component were mixed and stirred and dispersed uniformly, and then filled into a container to prepare a skin lotion.
Compounding ingredients Compounding amount (%)
-----------------------
(A)
Ethanol 10.0
Monolauric acid 5.0
Polyoxyethylene (20) sorbitan dibutylhydroxytoluene 0.01
Fragrance 0.05
(B)
Acteoside crude product of Example 1 0.5
(C)
Glycerin 5.0
Xanthan gum 0.1
Hydroxyethyl cellulose 0.1
Purified water balance
実施例8(スキンクリーム)
A成分とB成分を混合したものとを、それぞれ均一に加熱溶解して温度を80℃にする。次いで、これにC成分を注入乳化した後、攪拌しながら30℃まで冷却し、スキンクリームを調製した。
配合成分 配合量(%)
−−−−−−−−−−−−−−−−−−−−−−−
(A)
グリセリンモノステアレート 2.0
蜜ロウ 1.0
モノオレイン酸 6.0
ポリオキシエチレン(20)ソルビタン
ワセリン 4.0
流動パラフィン 12.0
(B)
実施例1のアクテオシド粗精製品 0.5
(C)
N−ステアロイル 1.0
−L−グルタミン酸ナトリウム
カラギーナン 0.3
メチルパラベン 0.1
精製水 残 量
Example 8 (skin cream)
The mixture of component A and component B is heated and dissolved uniformly to bring the temperature to 80 ° C. Next, component C was injected and emulsified therein, and then cooled to 30 ° C. with stirring to prepare a skin cream.
Compounding ingredients Compounding amount (%)
-----------------------
(A)
Glycerol monostearate 2.0
Honey wax 1.0
Monooleic acid 6.0
Polyoxyethylene (20) sorbitan petrolatum 4.0
Liquid paraffin 12.0
(B)
Acteoside crude product of Example 1 0.5
(C)
N-stearoyl 1.0
-Sodium L-glutamate carrageenan 0.3
Methylparaben 0.1
Purified water balance
実施例9(錠剤)
下記の各成分を均一に混合し、常法により錠剤を調製した。
配合成分 配合量(%)
−−−−−−−−−−−−−−−−−−−−−−−
アクテオシド(ChromaDex社製) 0.15
還元麦芽水飴 49.0
結晶セルロース 43.85
寒天末 4.0
香料 1.0
ショ糖脂肪酸エステル 2.0
Example 9 (tablet)
The following components were uniformly mixed, and tablets were prepared by a conventional method.
Compounding ingredients Compounding amount (%)
-----------------------
Acteoside (ChromaDex) 0.15
Reduced malt syrup 49.0
Crystalline cellulose 43.85
Agar powder 4.0
Fragrance 1.0
Sucrose fatty acid ester 2.0
実施例10(顆粒剤)
下記の各成分を均一に粉砕混合し、常法により顆粒剤を調製した。
配合成分 配合量(%)
−−−−−−−−−−−−−−−−−−−−−−−
実施例2のアクテオシド精製品 1.0
でんぷん 40.0
乳糖 58.0
結晶セルロース 1.0
Example 10 (granule)
The following components were uniformly ground and mixed, and granules were prepared by a conventional method.
Compounding ingredients Compounding amount (%)
-----------------------
Acteoside purified product of Example 2 1.0
Starch 40.0
Lactose 58.0
Crystalline cellulose 1.0
実施例11(ソフトカプセル剤)
下記の各成分を混合し、ゼラチンとグリセリンからなるゼラチン皮膜に充填し、常法によりソフトカプセル剤とした。
配合成分 配合量(%)
−−−−−−−−−−−−−−−−−−−−−−−
実施例2のアクテオシド精製品 3.0
大豆油 52.0
ビタミンE 20.0
小麦胚芽油 15.0
グリセリン脂肪酸エステル 5.0
ミツロウ 5.0
Example 11 (soft capsule)
The following components were mixed, filled into a gelatin film composed of gelatin and glycerin, and made into a soft capsule by a conventional method.
Compounding ingredients Compounding amount (%)
-----------------------
Acteoside purified product of Example 2 3.0
Soybean oil 52.0
Vitamin E 20.0
Wheat germ oil 15.0
Glycerin fatty acid ester 5.0
Beeswax 5.0
実施例12(ハードカプセル剤)
下記の各成分を混合し、ゼラチンからなるカプセル容器に充填し、常法によりハードカプセル剤とした。
配合成分 配合量(%)
−−−−−−−−−−−−−−−−−−−−−−−
実施例2のアクテオシド精製品 5.0
還元麦芽水飴 60.0
デキストリン 34.0
グリセリン脂肪酸エステル 1.0
Example 12 (hard capsule)
The following components were mixed and filled into a capsule container made of gelatin to obtain a hard capsule by a conventional method.
Compounding ingredients Compounding amount (%)
-----------------------
Acteoside purified product of Example 2 5.0
Reduced malt syrup 60.0
Dextrin 34.0
Glycerin fatty acid ester 1.0
実施例13(ドリンク剤)
下記の各成分を混合し、常法によりドリンク剤とした。
配合成分 配合量(%)
−−−−−−−−−−−−−−−−−−−−−−−
アクテオシド(ChromaDex社製) 0.004
還元麦芽水飴 20.0
エリスリトール 10.0
クエン酸 1.0
精製水 残 量
Example 13 (drink agent)
The following components were mixed and used as a drink by a conventional method.
Compounding ingredients Compounding amount (%)
-----------------------
Acteoside (ChromaDex) 0.004
Reduced malt syrup 20.0
Erythritol 10.0
Citric acid 1.0
Purified water balance
実施例14(ゼリー製剤)
下記の各成分を混合し、常法によりゼリー製剤とした。
配合成分 配合量(%)
−−−−−−−−−−−−−−−−−−−−−−−
実施例2のアクテオシド精製品 0.04
デキストリン 24.0
パラチノース 5.0
ゼラチン 1.0
ペクチン 0.5
イノシトール 5.0
クエン酸 0.8
アスコルビン酸 3.0
ニコチン酸アミド 0.01
精製水 残 量
Example 14 (jelly preparation)
The following components were mixed and made into a jelly preparation by a conventional method.
Compounding ingredients Compounding amount (%)
-----------------------
Acteoside purified product of Example 2 0.04
Dextrin 24.0
Palatinose 5.0
Gelatin 1.0
Pectin 0.5
Inositol 5.0
Citric acid 0.8
Ascorbic acid 3.0
Nicotinamide 0.01
Purified water balance
実施例15(チューインガム)
下記の各成分を混合し、常法によりチューインガムを調製した。
配合成分 配合量(%)
−−−−−−−−−−−−−−−−−−−−−−−
実施例1のアクテオシド粗精製品 1.0
ガムベース 25.0
マルチトール 45.0
マンニット 20.0
ソルビトール 5.0
香料 1.0
精製水 残 量
Example 15 (chewing gum)
The following components were mixed and a chewing gum was prepared by a conventional method.
Compounding ingredients Compounding amount (%)
-----------------------
Acteoside crude product of Example 1 1.0
Gum base 25.0
Maltitol 45.0
Mannit 20.0
Sorbitol 5.0
Fragrance 1.0
Purified water balance
実施例16(グミキャンディ)
下記の各成分を混合し、常法によりグミキャンディを調製した。
配合成分 配合量(%)
−−−−−−−−−−−−−−−−−−−−−−−
実施例1のアクテオシド粗精製品 1.0
グラニュー糖 34.0
水飴 30.0
ゼラチン 10.0
クエン酸 0.5
酒石酸 0.3
香料 1.0
精製水 残 量
Example 16 (Gummy Candy)
The following components were mixed and gummy candy was prepared by a conventional method.
Compounding ingredients Compounding amount (%)
-----------------------
Acteoside crude product of Example 1 1.0
Granulated sugar 34.0
Minamata 30.0
Gelatin 10.0
Citric acid 0.5
Tartaric acid 0.3
Fragrance 1.0
Purified water balance
本発明のシワ形成抑制剤は、外用塗布及び/又は経口摂取することで優れたシワ形成抑制作用を有し、水溶液、W/O型又はO/W型エマルション、錠剤、顆粒剤、各種カプセル剤、ドリンク製剤、固形剤等、任意の剤型とすることができる。化粧料としては、クリーム、乳液、化粧水、パック、ジェル、スティック、シート、パップとすることができる。また飲食物としては、飲料、ゼリー、チューインガム、キャンディ、錠菓等とすることができ、シワ形成抑制を目的とした用途に有用である。
The wrinkle formation inhibitor of the present invention has an excellent wrinkle formation inhibitory action when applied externally and / or taken orally, and is an aqueous solution, W / O type or O / W type emulsion, tablet, granule, various capsules , Drink preparations, solid preparations, etc. Cosmetics can be creams, emulsions, lotions, packs, gels, sticks, sheets, and papps. Moreover, as food and drink, it can be set as a drink, jelly, chewing gum, a candy, a tablet confectionery, etc., and it is useful for the use aiming at wrinkle formation suppression.
Claims (7)
An ingestion method comprising orally administering 0.001 g to 0.05 g of acteoside, which is an active ingredient of the wrinkle formation inhibitor according to any one of claims 1 to 4, per day.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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JP2005132793A JP2006306804A (en) | 2005-04-28 | 2005-04-28 | Wrinkle formation inhibitor |
PCT/EP2006/003119 WO2006114189A1 (en) | 2005-04-28 | 2006-04-06 | Anti-wrinkle composition |
Applications Claiming Priority (1)
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JP2005132793A JP2006306804A (en) | 2005-04-28 | 2005-04-28 | Wrinkle formation inhibitor |
Publications (1)
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Family
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JP2005132793A Pending JP2006306804A (en) | 2005-04-28 | 2005-04-28 | Wrinkle formation inhibitor |
Country Status (2)
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JP (1) | JP2006306804A (en) |
WO (1) | WO2006114189A1 (en) |
Cited By (6)
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JP2008280271A (en) * | 2007-05-09 | 2008-11-20 | Oriza Yuka Kk | Agent for preventing photoaging of skin |
JP2009067749A (en) * | 2007-09-14 | 2009-04-02 | Maruzen Pharmaceut Co Ltd | Matrix metalloprotease-1(mmp-1) inhibitor, matrix metalloprotease-2(mmp-2) inhibitor, estrogen-like action agent, profilaggrin production promoter, filaggrin production promoter, antiobese agent and cyclic amp phosphodiesterase activity inhibitor |
JP2009263279A (en) * | 2008-04-25 | 2009-11-12 | Oriza Yuka Kk | Elastase inhibitor |
JP2010510173A (en) * | 2006-10-17 | 2010-04-02 | ウォン,ハイロング | Cosmetic composition and preparation method and application thereof |
JP2013501512A (en) * | 2009-08-11 | 2013-01-17 | トトュム ビオ コスメティック | Method for producing whole olive juice, composition obtained by the method, and use of the composition in cosmetics and nutritional foods |
KR101356797B1 (en) * | 2012-02-02 | 2014-01-29 | (주)모아캠 | Extract Containing Acteoside Derived from Lippia citriodora and Cosmetic Composition Containing the Same |
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JP2008239505A (en) * | 2007-03-26 | 2008-10-09 | Oriza Yuka Kk | Neuroblast growth promoter and neurite extender |
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US20110144040A1 (en) * | 2009-12-10 | 2011-06-16 | MN Intellectual Property Corp, LLC | Acteoside and acteoside-rich plant extracts for increasing athletic performance in humans |
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JPH08119842A (en) * | 1994-01-21 | 1996-05-14 | Pola Chem Ind Inc | Ultraviolet light absorber |
JPH07223964A (en) * | 1994-02-01 | 1995-08-22 | Du Pont Merck Pharmaceut Co | Phospholipase a2 inhibitor |
FR2772235B1 (en) * | 1997-12-12 | 2000-07-21 | Fabre Pierre Sante | POLYPHENOLIC COMPOSITION, USEFUL AS A FOOD SUPPLEMENT, NUTRACEUTICAL OR COSMETIC COMPOSITION |
JP4067074B2 (en) * | 1999-03-09 | 2008-03-26 | 花王株式会社 | Skin cosmetics |
WO2001034169A1 (en) * | 1999-11-11 | 2001-05-17 | Dietrich Paper | Use of an extract from plantago lanceolata |
JP2001252054A (en) * | 2000-01-07 | 2001-09-18 | Kanebo Ltd | Food composition |
JP3882106B2 (en) * | 2000-12-06 | 2007-02-14 | 三栄源エフ・エフ・アイ株式会社 | Fading inhibitor |
FR2825022B1 (en) * | 2001-05-23 | 2005-01-14 | Seppic Sa | COMPOSITION OF OLIVE POLYPHENOLS. USE AS A COSMETIC AND DIETETIC ACTIVE |
FR2850572B1 (en) * | 2003-02-03 | 2005-04-01 | Rocher Yves Biolog Vegetale | USE OF VERBASCOSIDE AS AGENT STIMULATING THE SYNTHESIS OF THERMAL SHOCK PROTEINS BY SKIN CELLS |
JP2005029481A (en) * | 2003-07-09 | 2005-02-03 | Kao Corp | Oral prophylactic and ameliorating agent for wrinkle formation |
JP2005082522A (en) * | 2003-09-08 | 2005-03-31 | Kanebo Cosmetics Inc | Bleaching cosmetic |
-
2005
- 2005-04-28 JP JP2005132793A patent/JP2006306804A/en active Pending
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2006
- 2006-04-06 WO PCT/EP2006/003119 patent/WO2006114189A1/en active Application Filing
Cited By (6)
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JP2010510173A (en) * | 2006-10-17 | 2010-04-02 | ウォン,ハイロング | Cosmetic composition and preparation method and application thereof |
JP2008280271A (en) * | 2007-05-09 | 2008-11-20 | Oriza Yuka Kk | Agent for preventing photoaging of skin |
JP2009067749A (en) * | 2007-09-14 | 2009-04-02 | Maruzen Pharmaceut Co Ltd | Matrix metalloprotease-1(mmp-1) inhibitor, matrix metalloprotease-2(mmp-2) inhibitor, estrogen-like action agent, profilaggrin production promoter, filaggrin production promoter, antiobese agent and cyclic amp phosphodiesterase activity inhibitor |
JP2009263279A (en) * | 2008-04-25 | 2009-11-12 | Oriza Yuka Kk | Elastase inhibitor |
JP2013501512A (en) * | 2009-08-11 | 2013-01-17 | トトュム ビオ コスメティック | Method for producing whole olive juice, composition obtained by the method, and use of the composition in cosmetics and nutritional foods |
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