JP2019131548A - Composition - Google Patents
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- Publication number
- JP2019131548A JP2019131548A JP2019015221A JP2019015221A JP2019131548A JP 2019131548 A JP2019131548 A JP 2019131548A JP 2019015221 A JP2019015221 A JP 2019015221A JP 2019015221 A JP2019015221 A JP 2019015221A JP 2019131548 A JP2019131548 A JP 2019131548A
- Authority
- JP
- Japan
- Prior art keywords
- oil
- carotenoid
- asteraceae
- astaxanthin
- composition
- 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.)
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Abstract
Description
本発明は、カロテノイドと特定の植物から得られる油剤及びニコチン酸アミドを含有することを特徴とする組成物に関する。そして、本発明は特定の植物から得られる油剤によるカロテノイドの安定化剤及びカロテノイドの安定化方法に関する。 The present invention relates to a composition comprising a carotenoid, an oil obtained from a specific plant, and nicotinamide. The present invention also relates to a carotenoid stabilizer using an oil agent obtained from a specific plant and a carotenoid stabilization method.
アスタキサンチン等のカロテノイドは、老化防止、シミの予防・改善等の肌に有用な効果を有することが知られている。カロテノイドは、天然に存在する黄色から赤のテルペノイド類の色素で、植物類、藻類、及びバクテリアに見つけることができる。カロテノイドの一種であるアスタキサンチン類(アスタキサンチンおよびそのエステル等も含む)は、自然界では動植物界に広く分布しており、主として養殖魚や養鶏の色揚げ剤として使用されている。また、アスタキチンサン類は、酸化防止効果、抗炎症効果(特許文献1、特許文献2参照)、皮膚老化防止効果(特許文献3参照)などの機能を有することも知られている。このため、アスタキチンサン類を食品、化粧料、医薬品の原材料及びそれらの加工品等へ添加することが検討・実施されている。 It is known that carotenoids such as astaxanthin have useful effects on the skin such as prevention of aging and prevention / improvement of spots. Carotenoids are naturally occurring yellow to red terpenoid pigments that can be found in plants, algae, and bacteria. Astaxanthins (including astaxanthin and esters thereof), which is a kind of carotenoid, are widely distributed in the animal and plant kingdoms in nature, and are mainly used as a color frying agent for farmed fish and chickens. In addition, astaxanthin is also known to have functions such as an antioxidant effect, an anti-inflammatory effect (see Patent Document 1 and Patent Document 2), and an anti-skin aging effect (see Patent Document 3). For this reason, it has been studied and implemented to add astaxanthins to foods, cosmetics, raw materials for pharmaceuticals and processed products thereof.
また、ニコチン酸アミドは、ニコチンアミド、ナイアシンアミドともよばれる、ニコチン酸の誘導体であり、ニコチン酸欠乏症の予防及び治療等に利用されている。また、肌あれ改善、美白効果、抗老化効果などが知られており、ニコチン酸アミドとアスタキサンチン類とを組み合わせることで、より優れた抗老化化粧料等の開発が期待される。 Nicotinamide is a derivative of nicotinic acid, also called nicotinamide or niacinamide, and is used for prevention and treatment of nicotinic acid deficiency. Furthermore, skin roughness improvement, whitening effect, anti-aging effect and the like are known, and development of more excellent anti-aging cosmetics and the like is expected by combining nicotinamide and astaxanthins.
一方、アスタキサンチン等のカロテノイドは構造的に不安定であり、熱、光、酸化などにより劣化が促進されることが知られており、製剤に安定に含有させることが困難である。そのため、これまでに安定化剤としてアスコルビン酸と併用する技術や、硬質カプセルによる包接等の工夫がなされてきたほか(特許文献4参照)、特定の油溶性植物エキスとアルコールとナッツポリフェノールおよびキレート剤とを組み合わせる方法(特許文献5参照)や、有機酸をカロテノイド含有組成物に添加する方法(特許文献6参照)、鉄イオン、鉄キレート剤、ジブロピレングリコール、水溶性酸化防止剤との併用(特許文献7参照)、赤ワインエキスやコラーゲンペプチドとの併用(特許文献8参照)などによる、アスタキサンチン等のカロテノイドの安定化方法が開示されている。 On the other hand, carotenoids such as astaxanthin are structurally unstable, and it is known that deterioration is accelerated by heat, light, oxidation, etc., and it is difficult to stably contain them in a preparation. Therefore, in addition to the technology used in combination with ascorbic acid as a stabilizer and the inclusion such as inclusion with hard capsules (see Patent Document 4), specific oil-soluble plant extracts, alcohols, nut polyphenols and chelates In combination with an agent (see Patent Document 5), a method of adding an organic acid to a carotenoid-containing composition (see Patent Document 6), iron ion, iron chelating agent, dibromopyrene glycol, water-soluble antioxidant (See Patent Document 7), a method for stabilizing carotenoids such as astaxanthin by using a combination of red wine extract or collagen peptide (see Patent Document 8) is disclosed.
しかしながら、これらの方法はいずれも安定化剤が高価であったり、安定化の効果が十分でなかったり、あるいは安定化剤が水溶性成分である場合はアスタキサンチン等のカロテノイドを溶解させる油性成分への分散が困難であり十分な効果が発揮できない等の問題があった。さらに、有用な効果を有することが知られているアスタキサンチン等のカロテノイドの安定性を高め、その効果を長期にわたって持続させるという観点からみた場合に満足のいくものではなかった。 However, in any of these methods, the stabilizer is expensive, the effect of stabilization is not sufficient, or when the stabilizer is a water-soluble component, the oil component that dissolves carotenoids such as astaxanthin is dissolved. There was a problem that dispersion was difficult and sufficient effects could not be exhibited. Furthermore, it was not satisfactory from the viewpoint of enhancing the stability of carotenoids such as astaxanthin, which are known to have useful effects, and sustaining the effects over a long period of time.
また、発明者らは、肌あれ改善、美白効果、抗老化効果などにより優れた組成物を得るために、カロテノイドを含有する組成物にニコチン酸アミドを含有させることを試みたが、熱、光、酸化などによるカロテノイドの劣化が促進されてしまうことが分かった。 In addition, the inventors tried to contain nicotinamide in a composition containing carotenoids in order to obtain a composition excellent in improving skin roughness, whitening effect, anti-aging effect, etc. It was found that deterioration of carotenoids due to oxidation and the like was promoted.
本発明が解決しようとする課題は、老化防止等に有用であることが知られているアスタキサンチン等のカロテノイドの劣化を抑制し、その効果を長期にわたって維持させるための安定化剤や安定化方法を提供することである。さらに、抗老化効果等により優れた化粧料等を得るために、カロテノイドを含有する組成物にニコチン酸アミドを含有させた場合に生じるカロテノイドの劣化促進を抑制し、その効果を長期にわたって維持させた組成物の提供である。 The problem to be solved by the present invention is to provide a stabilizer and a stabilization method for suppressing deterioration of carotenoids such as astaxanthin, which are known to be useful for preventing aging, and maintaining the effect for a long period of time. Is to provide. Furthermore, in order to obtain cosmetics and the like that are superior in anti-aging effects, etc., the carotenoid-containing composition contains nicotinic acid amide, which suppresses the promotion of carotenoid degradation and maintains its effect over a long period of time. Providing a composition;
かかる実情に鑑み、本発明者らは上記課題を解決すべく鋭意検討した結果、アスタキサンチン等のカロテノイドと特定の植物から得られる油剤とを組み合わせることにより、アスタキサンチン等のカロテノイドの光による褪色の防止等の安定化に著しい効果を発揮することを見出し、本発明を完成するに至った。また、ニコチン酸アミドを含有させた際に生じるカロテノイドの劣化促進においても著しい抑制効果を発揮することを見出した。 In view of such a situation, the present inventors have intensively studied to solve the above problems, and as a result, by combining a carotenoid such as astaxanthin and an oil obtained from a specific plant, prevention of fading due to light of the carotenoid such as astaxanthin, etc. It has been found that it exhibits a remarkable effect on stabilization of the present invention, and the present invention has been completed. It has also been found that a remarkable inhibitory effect is exerted in promoting the deterioration of carotenoids produced when nicotinamide is contained.
すなわち、本発明は次の成分(a)〜(c);
(a)カロテノイド
(b)イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤
(c)ニコチン酸アミド
を含有する組成物に関するものである。
That is, the present invention includes the following components (a) to (c);
(A) Carotenoid (b) Contains oil agent (c) nicotinic acid amide obtained from one or more plants selected from the family Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Asteraceae, Spiraceae, Simondiaceae, Acetaceae It is related with the composition to do.
前記成分(a)がアスタキサンチン類である前記記載の組成物に関するものである。 The said component (a) is related with the said composition of astaxanthin.
前記成分(b)が、イネ科イネ属、イネ科ジュズダマ属、シソ科シソ属、ゴマ科ゴマ属、ツバキ科ツバキ属、キク科ベニバナ属、モクセイ科オリーブ属、シモンジア科シモンジア属、アカテツ科アルガンノキ属から選ばれる1種以上の植物から得られる油剤である前記記載の組成物に関するものである。 The component (b) is the genus Gramineae, Gramineae Zuzudama, Lamiaceae Perilla, Sesame Sesame, Camellia Camellia, Asteraceae Safflower, Asteraceae Olive, Simmonidae Simmonia, Acatezaceae Arganoki It is related with the said composition which is an oil agent obtained from the 1 or more types of plant chosen from a genus.
前記成分(b)が、コメ胚芽油、コメヌカ油、エゴマ油、ゴマ種子油、ツバキ種子油、ハトムギ油、サフラワー油、オリーブ果実油、ホホバ油、アルガンオイルから選ばれる1種以上である前記記載の組成物に関するものである。 Said component (b) is at least one selected from rice germ oil, rice bran oil, sesame oil, sesame seed oil, camellia seed oil, pearl barley oil, safflower oil, olive fruit oil, jojoba oil, argan oil It relates to the composition described.
前記組成物が、化粧料又は皮膚外用剤である前記記載の組成物に関するものである。 The said composition is related with the said composition which is cosmetics or a skin external preparation.
イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤を有効成分とするカロテノイドの安定化剤に関するものである。 The present invention relates to a carotenoid stabilizer comprising as an active ingredient an oil agent obtained from one or more plants selected from the family of Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Asteraceae, Spiraceae, Simmondiaceae, and Acetaceae.
カロテノイドを含有する組成物に、イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤を添加することを特徴とするカロテノイドの安定化方法に関するものである。 It is characterized by adding to the composition containing carotenoid an oil agent obtained from one or more kinds of plants selected from the family Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Asteraceae, Spiraceae, Simondiaceae, Acetaceae The present invention relates to a method for stabilizing carotenoids.
カロテノイド及びニコチン酸アミドを含有する組成物にイネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤を添加するカロテノイド安定化方法に関するものである。 A carotenoid in which an oil agent obtained from one or more plants selected from the family Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Asteraceae, Asteraceae, Simondiaceae, Acatezaceae is added to a composition containing carotenoid and nicotinamide It relates to a stabilization method.
本発明の組成物、安定化剤及び安定化方法は、アスタキサンチン類等のカロテノイドの劣化を抑制することでアスタキサンチン類等のカロテノイドの効果を有効に発揮させることができる。 The composition, stabilizer and stabilization method of the present invention can effectively exert the effects of carotenoids such as astaxanthins by suppressing the degradation of carotenoids such as astaxanthins.
以下、本発明を詳細に説明する。なお、本明細書において、「〜」はその前後の数値を含む範囲を意味するものとする。 Hereinafter, the present invention will be described in detail. In the present specification, “to” means a range including numerical values before and after.
本発明における成分(a)のカロテノイドは、植物類、藻類及びバクテリアのいずれのものも含まれる。また天然由来のものに限定されず、常法に従って得られるものであればいずれのものも本発明におけるカロテノイドに包含される。 In the present invention, the carotenoid of component (a) includes any of plants, algae and bacteria. Moreover, it is not limited to the thing of natural origin, Any thing will be included by the carotenoid in this invention if it is obtained according to a conventional method.
カロテノイドとしては、炭化水素類(カロテン類)及びこれらの酸化アルコール誘導体類(キサントフィル類)並びにこれらのエステルが挙げられる。本発明では特に断らない限り、これらの化合物を含めて「カロテノイド」と称する。カロテノイドの例としては、アクチニオエリスロール、アスタキサンチン、ビキシン、カンタキサンチン、カプサンチン、カプソルビン、β−8’−アポ−カロテナール(アポカロテナール)、β−12’−アポ−カロテナール、α−カロテン、β−カロテン、”カロテン”(α−及びβ−カロテン類の混合物)、γ−カロテン、δ−カロテン、β−クリプトキサンチン、エキネノン、パーム油カロテン、ルテイン、リコピン、ビオレリトリン、ゼアキサンチン、フコキサンチン及びそれらのうちヒドロキシル又はカルボキシルを含有するもののエステル類を挙げることができる。 Examples of carotenoids include hydrocarbons (carotenes), oxidized alcohol derivatives thereof (xanthophylls), and esters thereof. In the present invention, these compounds are referred to as “carotenoid” unless otherwise specified. Examples of carotenoids include actinioerythrol, astaxanthin, bixin, canthaxanthin, capsanthin, capsorubin, β-8′-apo-carotenal (apocarotenal), β-12′-apo-carotenal, α-carotene, β-carotene , “Carotene” (a mixture of α- and β-carotenes), γ-carotene, δ-carotene, β-cryptoxanthine, echinone, palm oil carotene, lutein, lycopene, biorelythrin, zeaxanthin, fucoxanthin and among them hydroxyl Or ester of what contains carboxyl can be mentioned.
本発明に用いられるカロテノイドとしては、好ましくは常温で液状のものである。特に好ましい例としては、酸化防止効果、抗炎症効果、皮膚老化防止効果、美白効果などを有し、黄色から赤色の範囲の着色料として知られているアスタキサンチン類である。 The carotenoid used in the present invention is preferably liquid at room temperature. Particularly preferred examples are astaxanthins that have an antioxidant effect, an anti-inflammatory effect, a skin aging prevention effect, a whitening effect, and the like and are known as colorants in the yellow to red range.
アスタキサンチンは、476nm(エタノール)、468nm(ヘキサン)に吸収極大を持つ赤色の色素でキサントフィル類に分類され、化学構造は3,3’−dihydroxy−β,β−carotene−4,4’−dione(C40H5204、分子量596.82)である。本発明においては、特に断らない限り、上記のアスタキサンチン及びアスタキサンチンエステル等の誘導体を含めて「アスタキサンチン類」と称する。 Astaxanthin is a red pigment having an absorption maximum at 476 nm (ethanol) and 468 nm (hexane), and is classified into xanthophylls, and its chemical structure is 3,3′-dihydroxy-β, β-carotene-4, 4′-dione ( C 40 H 52 0 4 , molecular weight 596.82). In the present invention, the term “astaxanthin” includes the above-mentioned derivatives such as astaxanthin and astaxanthin ester unless otherwise specified.
本発明に用いられるアスタキサンチン類は、例えば、オキアミ、サケ、マス、福寿草、赤色酵母、ヘマトコッカス藻等の天然物から抽出したものや合成品を用いることができるが、ヘマトコッカス藻から抽出されたもの(以下、ヘマトコッカス藻抽出物ともいう)が、品質、生産性の点から特に好ましい。天然物からアスタキサンチンを得る場合の抽出溶媒については、水系溶媒でも有機溶媒であってもよい。有機溶媒としてはメタノール、エタノール、イソプロパノール、アセトン、1,3−ブチレングリコール、エチレングリコール、プロピレングリコール、グリセリン、酢酸エチル、エーテル、ヘキサン等を用いることができる。また、超臨界状態の二酸化炭素等を用いることもできる。これらの溶媒は単独で用いてもよいし2種類以上を混合して用いてもよい。 Astaxanthins used in the present invention can be extracted from natural products such as krill, salmon, trout, cypress, red yeast, hematococcus algae or synthetic products, but extracted from hematococcus algae. A thing (henceforth Haematococcus alga extract) is especially preferable from the point of quality and productivity. The extraction solvent for obtaining astaxanthin from a natural product may be an aqueous solvent or an organic solvent. As the organic solvent, methanol, ethanol, isopropanol, acetone, 1,3-butylene glycol, ethylene glycol, propylene glycol, glycerin, ethyl acetate, ether, hexane, or the like can be used. Also, carbon dioxide in a supercritical state can be used. These solvents may be used alone or in combination of two or more.
本発明に使用できるヘマトコッカス藻抽出物の由来としては、具体的には、ヘマトコッカス・プルビアリス(Haematococcus pluvialis)、ヘマトコッカス・ラキュストリス(Haematococcus lacustris)、ヘマトコッカス・カペンシス(Haematococcus capensis)、ヘマトコッカス・ドロエバゲンシス(Haematococcus droebakensis)、ヘマトコッカス・ジンバビエンシス(Haematococcus zimbabwiensis)等が挙げられる。また、広く市販されているヘマトコッカス藻抽出物を用いることができ、例えば、富士フィルム社製のASTOTS−S、同−5O、同−10O等、富士化学工業社製のアスタリールオイル50F、同5F等、オリザ油化社製のアスタキサンチン−5C、同20C、バイオアクティブズジャパン社製のアスタキサンチン5%オイル、バイオジェニック社製のAstabio(登録商標)AR1、AR5等が挙げられる。またオキアミ由来としては、マリン大王社製Astax−S等が挙げられる。 Specific examples of the origin of the Haematococcus alga extract usable in the present invention include Haematococcus pluvialis, Haematococcus lacustris, Haematococcus capensis, Haematococcus capensis, Examples thereof include Haematococcus droebakensis and Haematococcus zimbabwiensis. Further, commercially available Haematococcus alga extract can be used, for example, ASTOTS-S, -5O, -10O, etc. manufactured by Fuji Film, Asteryl Oil 50F manufactured by Fuji Chemical Industry Co., Ltd. And 5F, Astaxanthin-5C manufactured by Oriza Oil Chemical Co., Ltd., 20C, Astaxanthin 5% oil manufactured by Bioactives Japan, Astabio (registered trademark) AR1, AR5 manufactured by Biogenic, and the like. Moreover, as Krill origin, Marin Daio company Astax-S etc. are mentioned.
本発明における成分(a)の含有量は、特に限定されないが、酸化防止、老化防止、シミの予防・改善等の肌に有用な効果を発揮する等の観点から、好ましくは0.000001〜0.1質量%(以下単に「%」と示す)であり、より好ましくは0.00001〜0.01%である。抽出液を使用する場合は、溶質の量が上記範囲内であれば、その抽出液濃度等は何ら限定されるものではない。 Although content of the component (a) in this invention is not specifically limited, From a viewpoint of exhibiting a useful effect on skin, such as antioxidant, anti-aging, and the prevention and improvement of a spot, Preferably it is 0.000001-0. 0.1% by mass (hereinafter simply referred to as “%”), more preferably 0.00001 to 0.01%. When an extract is used, the concentration of the extract is not limited as long as the amount of solute is within the above range.
本発明における成分(b)のイネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤とは、各々の科に属する植物から得られる油性成分のことである。植物から油性成分を得る方法については、特に制限されず一般的な方法を利用できる。例えば、植物の根、根茎、茎、葉、花、果実、種子等、もしくはその混合物を圧搾する方法、もしくは、溶媒により抽出する方法等を用いることができる。抽出に用いられる溶媒としては、特に限定されないが、メタノール、エタノール、イソプロパノール、アセトン、1,3−ブチレングリコール、エチレングリコール、プロピレングリコール、グリセリン、酢酸エチル、エーテル、ヘキサン等を用いることができる。また、超臨界状態の二酸化炭素等を用いることもできる。これらの溶媒は単独で用いてもよいし2種類以上を混合して用いてもよい。上記溶媒による抽出物は液状、ペースト状、ゲル状、固形状、粉末状等のいずれの形態であってもよい。また、抽出物は調製後そのまま使用することができるが、濃縮または乾固またはスプレードライしたものを油や極性溶媒に再度溶解して用いてもよい。特に限定されないが、油性成分がより多く得られるなどの観点から、植物の根、根茎、茎、葉、花、果実、種子等、もしくはその混合物を圧搾する方法を用いることが特に好ましい。さらに、必要であれば本発明の効果に影響のない範囲でろ過、活性炭、イオン交換樹脂等を用いて、脱色、脱臭、脱塩などの処理を施して用いることもできる。また、限外ろ過やイオン交換クロマトグラフィー、ゲルろ過クロマトグラフィーなどの方法により分画して用いることもできる The oil agent obtained from one or more kinds of plants selected from the family Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Asteraceae, Solanumaceae, Simondiaceae, Acatezidae of component (b) in the present invention includes It is an oily component obtained from the plant to which it belongs. A method for obtaining an oily component from a plant is not particularly limited, and a general method can be used. For example, a method of squeezing plant roots, rhizomes, stems, leaves, flowers, fruits, seeds, or the like, or a mixture thereof, or a method of extracting with a solvent can be used. Although it does not specifically limit as a solvent used for extraction, Methanol, ethanol, isopropanol, acetone, 1, 3- butylene glycol, ethylene glycol, propylene glycol, glycerol, ethyl acetate, ether, hexane, etc. can be used. Also, carbon dioxide in a supercritical state can be used. These solvents may be used alone or in combination of two or more. The extract by the solvent may be in any form such as liquid, paste, gel, solid, and powder. Further, the extract can be used as it is after preparation, but it may be concentrated, dried or spray-dried and dissolved again in oil or polar solvent. Although not particularly limited, it is particularly preferable to use a method of squeezing plant roots, rhizomes, stems, leaves, flowers, fruits, seeds, etc., or a mixture thereof from the viewpoint of obtaining more oily components. Furthermore, if necessary, it can be used after being subjected to treatments such as decolorization, deodorization, and desalting using filtration, activated carbon, ion exchange resin and the like within a range not affecting the effects of the present invention. In addition, it can be fractionated and used by methods such as ultrafiltration, ion exchange chromatography and gel filtration chromatography.
イネ科植物とは、イネ科(Poaceae(Gramineae))に属する植物全体を含むものである。イネ科は約600属9500種以上からなる大型の科である。イネ科のほとんどは、細長い葉と茎(稈)をもった草本である。 The grass family plant includes the whole plant belonging to the grass family (Poaceae (Gramineae)). The Gramineae is a large family consisting of more than 9,500 species of about 600 genera. Most grasses are herbs with elongated leaves and stems.
イネ科の主な属としてモウチクソウ属(Phyllostachys)、イネ属(Oryza)、カラスムギ属(Avena)、モロコシ属(Sorghum)、サトウキビ属(Saccharum)、ジュズダマ属(Coix)、クマザサ属(Sasa)などがあるがこれらのいずれであっても使用でき、その産地や採取時期は特に限定されない。具体的な植物としては、特に限定されないが、マダケ(Phyllostachys bambusoides Siebold et Zucc.)、イネ(Oryza sativa L.)、カラスムギ(Avena fatua L.)、モロコシ(Sorghumbicolar Moench var.bicolor)、サトウキビ(Saccharum spontaneum L.var.arenicola Ohwi)、クマザサ(Sasa veitchii Rehder)、ジュズダマ(Coix lachrymal-jobi L.)、ハトムギ(Coix lachrymal-jobi L.)などがあげられる。使用部位も根、根茎、茎、葉、花、果実、種子など特に限定されないが、種子を用いるのが特に好ましい。特に限定されないが、経時での変臭、変色などの組成物の安定性確保の観点から、イネ属(Oryza)、ジュズダマ属(Coix)から得られる、コメ胚芽油、コメヌカ油、ハトムギ油を用いることが特に好ましい。市販品としては、オリザ玄米胚芽油―S(オリザ油化社製)、こめサラダ油(築野)(築野食品工業社製)、オリザトコトリエノール(オリザ油化社製)、ヨクイニン油(千葉製粉社製)等が挙げられ、1種又は2種以上を用いることができる。 Major genera of the family Gramaceae (Phyllostachys), Rice genus (Oryza), Oatza (Avena), Sorghum (Sorghum), Saccharum (Coix), Sasa (genus Sasa), etc. However, any of these can be used, and the production area and collection time are not particularly limited. Specific plants include, but are not limited to, mushroom (Phyllostachys bambusoides Siebold et Zucc.), Rice (Oryza sativa L.), oat (Avena fatua L.), sorghum (Sorghumbicolar Moench var.bicolor), sugarcane (Saccharum spontaneum L.var.arenicola Ohwi), Kumazasa (Sasa veitchii Rehder), Juzdama (Coix lachrymal-jobi L.), pearl barley (Coix lachrymal-jobi L.) and the like. The use site is not particularly limited, such as roots, rhizomes, stems, leaves, flowers, fruits and seeds, but it is particularly preferable to use seeds. Although it is not particularly limited, rice germ oil, rice bran oil, or barley oil obtained from the genus Oryza or Coix is used from the viewpoint of ensuring the stability of the composition such as odor and discoloration over time. It is particularly preferred. Commercially available products include Oriza Brown Rice Germ Oil-S (Orisa Oil Chemical Co., Ltd.), Rice Salad Oil (Tsukino) (Tsukino Food Industry Co., Ltd.), Orizatocotrienol (Orisa Oil Chemical Co., Ltd.), Yokuinin Oil (Chiba Flour Mills Co. 1 type or 2 types or more can be used.
シソ科植物とは、シソ科(Labiatae(Lamiaceae))に属する植物全体を含むものである。シソ科は約180属2500種がほとんど全世界に分布しているが、日本には32属97種が自生している。シソ科のほとんどは、草木で茎は四稜形だが、まれに低木になり、この場合の茎は広い。葉は十字対生で、拓葉はなく、植物体に精油を含むものが多い。がくの中に4個の種子を入れた分果になる。 The Labiatae plant includes the whole plant belonging to Labiatae (Labiatae (Lamiaceae)). There are about 180 genera and 2500 species distributed almost all over the world, while Japan has 32 genera and 97 species native to Japan. Most Lamiaceae are vegetation with four-ridged stems, but rarely become shrubs, and in this case the stems are wide. The leaves are cruciform, there are no takuya leaves, and many plants contain essential oils. It becomes the fruit which put four seeds in the gargle.
シソ科の主な属としては、ローズマリー属(Rosmarinus)、タツナミソウ属(Scutellaria)、ジャコウゾウ属(Chelonopsis)、オドリコウ属(Lamium)、アキギリ属(Salvia)、ハッカ属(Mentha)、シソ属(Perilla)、ヤマハッカ属(Isodon)、ラバンドゥラ属(Lavendura)などがあるがこれらのいずれであっても使用でき、その産地や採取時期は特に限定されない。具体的な植物としては、特に限定されないが、ローズマリー(Rosmarinus officinalis L.)、コガネヤナギ(Scutellaria baicalensis Georgi)、ジャコウゾウ(Chelonopsis moschata Miq.)、オドリコソウ(Lamium album L.)、セージ(Salvia officinalis L.)、ベニバナサルビア(Salvia coccinea L.)、ハッカ(Mentha arvensis L.)、シソ(Perilla frutescens Britton)、エゴマ(Perilla frutescens Britton)、ヒキオコシ(Isodn japonicus H Hara)、ラベンダー(Lavandula angustifolia)などが挙げられる。使用部位も根、根茎、茎、葉、花、果実、種子など特に限定されないが、種子を用いるのが特に好ましい。特に限定されないが、経時での変臭、変色などの組成物の安定性確保の観点から、シソ属(Perilla)から得られるエゴマ油を用いることが特に好ましい。市販品としては、エゴマ油(丸善製薬社製)、エゴマオイル(太田油脂社製)、エゴマ油(精製)(サミット製油社製)等が挙げられ、1種又は2種以上を用いることができる。 The major genera of the family Lamiaceae include Rosemaryus, Scutellaria, Chelonopsis, Lamium, Salvia, Mentha, Perilla ), Genus Isodon, genus Labandura, etc., but any of these can be used, and the production area and collection time are not particularly limited. Although it does not specifically limit as a specific plant, Rosemary (Rosmarinus officinalis L.), Scarella willow (Scutellaria baicalensis Georgi), Musk elephant (Chelonopsis moschata Miq.), Odorikosou (Lamium album L.), Sage (Salvia officinalis L.) ), Safflower salvia (Salvia coccinea L.), mint (Mentha arvensis L.), perilla (Perilla frutescens Britton), egoma (Perilla frutescens Britton), cassow (Isodn japonicus H Hara), lavender (Lavandula angustifolia) . The use site is not particularly limited, such as roots, rhizomes, stems, leaves, flowers, fruits and seeds, but it is particularly preferable to use seeds. Although not particularly limited, it is particularly preferable to use egoma oil obtained from Perilla from the viewpoint of ensuring the stability of the composition such as odor change and discoloration over time. Examples of commercially available products include sesame oil (manufactured by Maruzen Pharmaceutical Co., Ltd.), sesame oil (manufactured by Ota Oil & Fats Co., Ltd.), sesame oil (refined) (manufactured by Summit Oil Co., Ltd.), and the like, and one or more can be used. .
ゴマ科植物とは、ゴマ科(Pedaliaceae)に属する植物全体を含むものである。代表的な油料植物のゴマで知られるゴマ科は最大20属80種ともいわれる。ゴマ科の主な属としては、ゴマ属(Sesamum)、ヤハズカズラ属(Thunbergia)、オギノツメ属(Hygrophia)などがあるがこれらのいずれであっても使用でき、その産地や採取時期は特に限定されない。具体的な植物としては、特に限定されないが、ゴマ(Sesamum indicum L.)、ローレンカズラ(Thunbergia laurifolia Lindl)、オギノツメ(Hygrophila salicifolia Nees)などが挙げられる。使用部位も根、根茎、茎、葉、花、果実、種子など特に限定されないが種子を用いるのが特に好ましい。特に限定されないが、経時での変臭、変色などの組成物の安定性確保の観点から、ゴマ属(Sesamum)から得られるゴマ種子油を用いることが特に好ましい。市販品としては、精製ゴマ油(サミット製油社製)、金印純正ゴマ油(かどや製油社製)、純正ゴマ油(日清オイリオ社製)、オーガニックセサミ油(香栄興業社製)等が挙げられ、1種又は2種以上を用いることができる。 Sesame plant includes all plants belonging to Pedaliaceae. The sesame family known as sesame, a typical oil plant, is said to have a maximum of 20 genera and 80 species. The main genus of the sesame family includes Sesamum, Thunbergia, and Hygrophia, but any of these can be used, and the production area and collection time are not particularly limited. Specific examples of the plant include, but are not limited to, sesame (Sesamum indicum L.), Lorenka quail (Thunbergia laurifolia Lindl), and ogitsume (Hygrophila salicifolia Nees). The use site is not particularly limited, such as roots, rhizomes, stems, leaves, flowers, fruits, and seeds, but it is particularly preferable to use seeds. Although not particularly limited, it is particularly preferable to use sesame seed oil obtained from Sesamum from the viewpoint of ensuring the stability of the composition such as odor and discoloration over time. Commercially available products include refined sesame oil (manufactured by Summit Oil Co., Ltd.), gold seal genuine sesame oil (manufactured by Kadoya Oil Co., Ltd.), genuine sesame oil (manufactured by Nisshin Oil Rio Co., Ltd.), organic sesame oil (manufactured by Koei Kogyo Co., Ltd.), etc. 1 type (s) or 2 or more types can be used.
ツバキ科植物とは、ツバキ科(Theaceae)に属する植物全体を含むものである。ツバキ科は約28属種600種以上である。ツバキ科の主な属としてはツバキ属(Camellia)で、その産地や採取時期は特に限定されない。具体的な植物としては、特に限定されないが、ツバキまたはヤブツバキ(Camellia japonica L.)等が挙げられる。使用部位も根、根茎、茎、葉、花、果実、種子など特に限定されないが種子を用いるのが特に好ましい。特に限定されないが、経時での変臭、変色などの組成物の安定性確保の観点から、ツバキ属(Camellia)から得られるツバキ種子油を用いることが特に好ましい。市販品としては、ツバキ油(大島椿社製)、精製椿油(横関油脂社製)等が挙げられ、1種又は2種以上を用いることができる。 A camellia plant includes the whole plant which belongs to the camellia family (Theaceae). The camellia family has more than 600 species of about 28 genera. The main genus of Camellia is Camellia, and its production area and collection time are not particularly limited. Specific plants include, but are not limited to, camellia or camellia (Camellia japonica L.). The use site is not particularly limited, such as roots, rhizomes, stems, leaves, flowers, fruits, and seeds, but it is particularly preferable to use seeds. Although not particularly limited, it is particularly preferable to use camellia seed oil obtained from Camellia from the viewpoint of ensuring the stability of the composition such as odor change and color change over time. Examples of commercially available products include camellia oil (manufactured by Oshima Coffee Co., Ltd.), refined camellia oil (manufactured by Yokoseki Oil & Fat Co., Ltd.), and the like, and one or more can be used.
キク科植物とは、キク科(Asteraceae)に属する植物全体を含むものである。キク科は1100〜1200属に分類され、2万3000を超える種があるとされる大型の科である。キク科のほとんどは、多年草であるが、約7%は一年草、約3%は木本で本格的な高木もある。キク科の大まかな特徴は、密に集まった多数の小花とそれを取り巻く総苞片とで頭花を構成している。キク科の主な属としてはキク属(Chrysanthemum)、ムラサキバレンギク属(Echinacea)、ノコギリソウ属(Achillea)、ベニバナ属(Carthamus)、シカギク属(Matricaria)、ヨモギ属(Artemisia)、キンセンカ属(Calendula)などがあるがこれらのいずれであっても使用でき、その産地や採取時期は特に限定されない。具体的な植物としては、特に限定されないが、キク(Chrysanthemum morifolium Ramat)、ナツシロギク(Chrysanthemum Parthenium Pers.)、エキナセア・アングスティフォリア(Echinacea angustifolia DC.)、セイヨウノコギリソウ(Achillea millefolium L.)、ベニバナ(Carthamus tinctorius L. )、カミツレ(Matricaria chamomilla L. )、ヨモギ(Artemisia princeps Pampan)、トウキンセンカ(Calendula officinalis L. )などが挙げられる。使用部位も根、根茎、茎、葉、花、果実、種子など特に限定されないが種子を用いるのが特に好ましい。特に限定されないが、経時での変臭、変色などの組成物の安定性確保の観点から、ベニバナ属(Carthamus)から得られるサフラワー油を用いることが特に好ましい。市販品としては、日清ベニ花油(日清オイリオ社製)、サフラワーサラダ油(精製)(サミット製油社製)、オーガニックサフラワー油(SNOI社製)等が挙げられ、1種又は2種以上を用いることができる。 Asteraceae includes all plants belonging to the Asteraceae family. The Asteraceae is a large family that is classified into 1100-1200 genera and has more than 23,000 species. Most of the Asteraceae are perennials, but about 7% are annuals, about 3% are woody and some are full-fledged. The rough feature of the Asteraceae is a head flower composed of a large number of closely spaced florets and a total septum surrounding them. The main genus of the Asteraceae is Chrysanthemum, Echinacea, Achillea, Carthamus, Matricaria, Artemisia, Calendula, etc. However, any of these can be used, and the production area and collection time are not particularly limited. Although it does not specifically limit as a specific plant, Chrysanthemum morifolium Ramat, feverfew (Chrysanthemum Parthenium Pers.), Echinacea angustifolia (Echinacea angustifolia DC.), Achillea millefolium L. (Achillea millefolium L.), Carthamus tinctorius L.), chamomile (Matricaria chamomilla L.), mugwort (Artemisia princeps Pampan), eucalyptus (Calendula officinalis L.) and the like. The use site is not particularly limited, such as roots, rhizomes, stems, leaves, flowers, fruits, and seeds, but it is particularly preferable to use seeds. Although not particularly limited, it is particularly preferable to use safflower oil obtained from the genus Carthamus from the viewpoint of ensuring the stability of the composition such as odor change and color change over time. Examples of commercially available products include Nissin Beni Flower Oil (Nisshin Oilio Co., Ltd.), Saflower Salad Oil (refined) (Summit Oil Co., Ltd.), Organic Saflower Oil (SNOI Co., Ltd.), and the like. The above can be used.
モクセイ科植物とは、モクセイ科(Oleaceae)に属する植物全体を含むものである。モクセイ科は世界の熱帯から温帯にかけて約30属600種が見られ、日本には7属26種ほどが分布する。モクセイ科は、低木や木材になる高木、オリーブなどの果樹、ジャスミンなどの香料に用いられる低木を含む木本性の科で、つる性のものもある。モクセイ科の主な属としてはオリーブ属(Olea)、モクセイ属(Osmanthus)、ハシドイ属(Syringa)やフジウツギ属(Buddleja)などがあるがこれらのいずれであっても使用でき、その産地や採取時期は特に限定されない。具体的な植物としては、特に限定されないが、オリーブ(Olea europaeaL.)、キンモクセイ(Osmanthus fragrans Lour. Var. aurantiacus Makino)、フサフジウツギ(Buddeleja davidii Franch. )などが挙げられる。使用部位も根、根茎、茎、葉、花、果実、種子など特に限定されないが種子を用いるのが特に好ましい。特に限定されないが、経時での変臭、変色などの組成物の安定性確保の観点から、オリーブ属(Olea)から得られるオリーブ果実油を用いることが特に好ましい。市販品としては、精製オリーブ油(日油社製)、精製オリーブ油(サミット製油社製)、オーガニック精製オリーブ油(香栄興業社製)等が挙げられ、1種又は2種以上を用いることができる。 The oleaceae plant includes all plants belonging to the oleaceae family (Oleaceae). There are about 30 genera and 600 species from the world tropical to temperate, and about 26 species of 7 genera are distributed in Japan. The oleaceae is a woody family that includes shrubs, tall trees that become timber, fruit trees such as olives, and shrubs used in perfumes such as jasmine. The main genus of the family Oxaceae includes the genus Olive (Olea), the genus Osmanthus, the genus Syringa, and the genus Buddleja. Is not particularly limited. Specific examples of the plant include, but are not limited to, olives (Olea europaea L.), betel oysters (Osmanthus fragrans Lour. Var. Aurantiacus Makino), and Fusafujitsugi (Buddeleja davidii Franch.). The use site is not particularly limited, such as roots, rhizomes, stems, leaves, flowers, fruits, and seeds, but it is particularly preferable to use seeds. Although not particularly limited, it is particularly preferable to use olive fruit oil obtained from Olea, from the viewpoint of ensuring the stability of the composition such as odor change and color change over time. Examples of commercially available products include refined olive oil (manufactured by NOF Corporation), refined olive oil (produced by Summit Oil Co., Ltd.), and organic refined olive oil (produced by Koei Kogyo Co., Ltd.), and one or more kinds can be used.
シモンジア科植物とは、シモンジア科(Simmondsiaceae)に属する植物全体を含むものである。シモンジア科はシモンジア科シモンジア属に属するシムモンドシア・キネシスただ1種からなる木本性の科である。シムモンドシア・キネシス(Simmondsia chinensis)は、ホホバとも呼ばれる。高いものでも3メートルにしかならないが、200年以上も生存している個体もある。種子はオイル(液体蝋)を含む。産地や採取時期は特に限定されず、使用部位も根、根茎、茎、葉、花、果実、種子など特に限定されないが種子を用いるのが特に好ましい。特に限定されないが、経時での変臭、変色などの組成物の安定性確保の観点から、シモンジア属から得られるホホバ油を用いることが特に好ましい。市販品としては、精製ホホバ油(香栄興業社製)、オーガニック精製ホホバ油(香栄興業社製)、ホホバ油(精製)(サミット製油社製)等が挙げられ、1種又は2種以上を用いることができる。 Simmondiaceae plants include all plants belonging to the Simmondsiaceae family. Simmondiaceae is a woody family consisting of only one species of Simmondsia kinesis, belonging to the genus Simmonia. Simmondsia chinensis is also called jojoba. Even tall ones are only 3 meters, but some individuals have survived for over 200 years. Seeds contain oil (liquid wax). There are no particular restrictions on the production area or the collection time, and the use site is not particularly limited, such as roots, rhizomes, stems, leaves, flowers, fruits, and seeds, but it is particularly preferable to use seeds. Although not particularly limited, it is particularly preferable to use jojoba oil obtained from the genus Simmonia from the viewpoint of ensuring the stability of the composition such as odor change and color change over time. Examples of commercially available products include refined jojoba oil (manufactured by Koei Kogyo Co., Ltd.), organic refined jojoba oil (manufactured by Koei Kogyo Co., Ltd.), jojoba oil (refined) (manufactured by Summit Oil Co., Ltd.), and the like. Can be used.
アカテツ科植物とは、アカテツ科(Sapotaceae)に属する植物全体を含むものである。アカテツ科は53属約1100種以上からなる大型の科である。アカテツ科の樹木は、高さ40メートルにもなる熱帯多雨林の巨大高木から森林の下層をなす小高木、さらには乾燥地域に生え、とげのある低木の種までさまざまである。アカテツ科の主な属としてはアルガンノキ属(Argania)、シアバターノキ属(Vitellaria)などがあるがこれらのいずれであっても使用でき、その産地や採取時期は特に限定されない。具体的な植物としては、特に限定されないが、アルガニア・スピノサ(Argania spinosa)、シアバターノキ(Vitellaria paradoxa)などが挙げられる。使用部位も根、根茎、茎、葉、花、果実、種子など特に限定されないが種子を用いるのが特に好ましい。特に限定されないが、経時での変臭、変色などの組成物の安定性確保の観点から、アルガンノキ属(Argania)から得られるアルガンオイルを用いることが特に好ましい。市販品としては、アルガンオイル(ニュートリッション・アクト社製)、アルガンオイル(BASF社製)、ARGAN OIL(DSM社製)等が挙げられ、1種又は2種以上を用いることができる。 The Acateaceae plant includes all plants belonging to the Sacateaceae family. The Acatezaceae is a large family consisting of more than 1,100 species of 53 genera. Trees of the Acatezaceae range from a huge tropical rainforest that is as high as 40 meters to a small tree that forms the bottom of the forest, as well as species of thorny shrubs that grow in dry areas. The main genera of the Acetaceae family include the genus Arganania and the genus Vitellaria, but any of these can be used, and the production area and collection time are not particularly limited. Specific plants include, but are not limited to, Argania spinosa, Vitellaria paradoxa, and the like. The use site is not particularly limited, such as roots, rhizomes, stems, leaves, flowers, fruits, and seeds, but it is particularly preferable to use seeds. Although not particularly limited, it is particularly preferable to use an argan oil obtained from the genus Argania from the viewpoint of ensuring the stability of the composition such as odor change and color change over time. Examples of commercially available products include argan oil (manufactured by Nutrition Act), argan oil (manufactured by BASF), and ARGAN OIL (manufactured by DSM), and one or more of them can be used.
本発明における成分(b)の含有量は、特に限定されず、成分(a)の安定化効果を発揮することができるという観点から、0.0001〜70%となることが好ましく、より好ましくは0.0005〜50%であり、さらに好ましくは、0.001〜10%である。 The content of the component (b) in the present invention is not particularly limited, and is preferably 0.0001 to 70%, more preferably from the viewpoint that the stabilizing effect of the component (a) can be exhibited. It is 0.0005-50%, More preferably, it is 0.001-10%.
また、成分(a)と成分(b)の含有質量割合は、特に限定されないが、成分(a)の安定化の効果に優れるという観点から、(b)/(a)=0.01〜500000であることが好ましく、0.1〜300000であることがより好ましく、0.1〜200000であると特に好ましい。 Further, the content mass ratio of the component (a) and the component (b) is not particularly limited, but (b) / (a) = 0.01 to 500,000 from the viewpoint that the effect of stabilizing the component (a) is excellent. It is preferable that it is 0.1-300,000, and it is especially preferable that it is 0.1-200000.
本発明における成分(c)のニコチン酸アミドとは、ニコチン酸(ビタミンB3、ナイアシンともよばれる)のアミド化合物であり、ニコチンアミド、ナイアシンアミドともよばれる、ニコチン酸の誘導体である。ニコチン酸アミドは水溶性ビタミンで、ビタミンB群の一つである公知の物質であり、天然物(米ぬかなど)から抽出されたり、あるいは公知の方法によって合成することができる。具体的には、第15改正日本薬局方2008に収載されているものを用いることが出来る。 The nicotinic acid amide of component (c) in the present invention is an amide compound of nicotinic acid (also called vitamin B3 or niacin), and is a derivative of nicotinic acid also called nicotinamide or niacinamide. Nicotinamide is a water-soluble vitamin and is a known substance that is one of the vitamin B groups, and can be extracted from a natural product (rice bran or the like) or synthesized by a known method. Specifically, those listed in the 15th revision Japanese Pharmacopoeia 2008 can be used.
本発明における成分(c)の含有量は、特に限定されず、抗老化作用に優れるという観点から、0.01〜10%であることが好ましく、0.5〜8%であることがより好ましく、1〜6%であることが特に好ましい。 The content of the component (c) in the present invention is not particularly limited, and is preferably 0.01 to 10%, more preferably 0.5 to 8% from the viewpoint of excellent anti-aging action. 1 to 6% is particularly preferable.
また、成分(b)と成分(c)の含有質量割合は、特に限定されないが、成分(a)の安定化効果に優れ、成分(c)に由来するべたつきを抑えることができるという観点から、(b)/(c)=0.00001〜1000であることが好ましく、0.0005〜500であることがより好ましく、0.0001〜100であることが特に好ましい。 Moreover, although the content mass ratio of a component (b) and a component (c) is not specifically limited, From the viewpoint that it is excellent in the stabilization effect of a component (a) and can suppress the stickiness originating in a component (c), (B) / (c) = 0.00001 to 1000 is preferable, 0.0005 to 500 is more preferable, and 0.0001 to 100 is particularly preferable.
成分(a)と成分(c)の含有質量割合は、特に限定されないが、成分(a)の安定化効果に優れるという観点から、(c)/(a)=1〜500000であることが好ましく、10〜300000であることがより好ましく、100〜200000であることが特に好ましい。 The content mass ratio of the component (a) and the component (c) is not particularly limited, but is preferably (c) / (a) = 1 to 500,000 from the viewpoint of being excellent in the stabilizing effect of the component (a). 10 to 300,000 is more preferable, and 100 to 200,000 is particularly preferable.
さらに本発明には、成分(d)として、アルコール類を含有させると、成分(c)の成分(a)及び(b)への分散性に優れるため、より好ましい。アルコール類としては、化粧料、皮膚外用剤、食品、インク、洗剤、衣料用柔軟仕上剤、芳香剤、消臭剤、織物等に使用されているものであれば、特に限定されず用いることができる。例えば、エタノール、n−プロピルアルコール、イソプロピルアルコール、n−ブチルアルコール等の低級アルコール、プロピレングリコール、ジプロピレングリコール、1,3−ブチレングリコール、グリセリン、ジグリセリン、1,2−ペンタンジオール、エチレングリコール、ポリエチレングリコール等の多価アルコール等が挙げられ、これらを1種又は2種以上用いることができる。これらの中でも、成分(c)の成分(a)及び(b)への分散性により優れる等の観点から、低級アルコールを用いることが好ましく、エタノールを用いることが特に好ましい。 Further, in the present invention, it is more preferable to add an alcohol as the component (d) because the dispersibility of the component (c) in the components (a) and (b) is excellent. Alcohols are not particularly limited as long as they are used in cosmetics, external preparations for skin, foods, inks, detergents, softeners for clothing, fragrances, deodorants, fabrics, and the like. it can. For example, lower alcohols such as ethanol, n-propyl alcohol, isopropyl alcohol, n-butyl alcohol, propylene glycol, dipropylene glycol, 1,3-butylene glycol, glycerin, diglycerin, 1,2-pentanediol, ethylene glycol, Examples thereof include polyhydric alcohols such as polyethylene glycol, and one or more of these can be used. Among these, from the viewpoint of excellent dispersibility of the component (c) in the components (a) and (b), it is preferable to use a lower alcohol, and it is particularly preferable to use ethanol.
本発明におけるの成分(d)の含有量は、特に限定されないが、成分(c)の成分(a)及び(b)への分散性により優れる等の観点から、0.1〜50%であることが好ましく、1〜40%であることが好ましく、5〜30%であることが特に好ましい。 Although content of the component (d) in this invention is not specifically limited, From a viewpoint of being excellent by the dispersibility to the component (a) and (b) of a component (c), it is 0.1 to 50%. It is preferably 1 to 40%, particularly preferably 5 to 30%.
また、成分(c)と成分(d)の含有質量割合は、特に限定されないが、成分(c)の成分(a)及び(b)への分散性により優れる等の観点から、(d)/(c)=0.1〜100であることが好ましく、0.5〜60であることがより好ましく、1〜45であることが特に好ましい。 Further, the content mass ratio of the component (c) and the component (d) is not particularly limited, but from the viewpoint of being excellent in dispersibility of the component (c) in the components (a) and (b), (d) / (C) is preferably 0.1 to 100, more preferably 0.5 to 60, and particularly preferably 1 to 45.
本発明の組成物には、必要に応じて本発明の効果を損なわない範囲で、上記成分の他に、化粧料、皮膚外用剤、食品、インク、洗剤、衣料用柔軟仕上剤、芳香剤、消臭剤、織物等の製剤に使用される成分、すなわち、水(精製水、温泉水、深層水等)、油剤、界面活性剤、金属セッケン、ゲル化剤、粉体、水溶性高分子、皮膜形成剤、樹脂、紫外線防御剤、包接化合物、抗菌剤、香料、消臭剤、塩類、pH調整剤、清涼剤、動物・微生物由来抽出物、植物抽出物、血行促進剤、収斂剤、抗脂漏剤、美白剤、抗炎症剤、活性酸素消去剤、細胞賦活剤、保湿剤、キレート剤、角質溶解剤、酵素、ホルモン類、ビタミン類等を加えることができる。 In the composition of the present invention, in addition to the above components, cosmetics, external preparations for skin, foods, inks, detergents, softeners for clothing, fragrance, Ingredients used in preparations such as deodorants and fabrics, that is, water (purified water, hot spring water, deep water, etc.), oil agents, surfactants, metal soaps, gelling agents, powders, water-soluble polymers, Film-forming agents, resins, UV protection agents, inclusion compounds, antibacterial agents, fragrances, deodorants, salts, pH adjusters, refreshing agents, animal / microbe-derived extracts, plant extracts, blood circulation promoters, astringents, Antiseborrheic agents, whitening agents, anti-inflammatory agents, active oxygen scavengers, cell activators, moisturizers, chelating agents, keratolytic agents, enzymes, hormones, vitamins and the like can be added.
本発明の組成物の製造方法は、特に限定されず、常法により調製される。例えば、上記成分(a)〜(d)さらに必要に応じて上記任意成分を加え、これを混合することにより調製する方法が挙げられる。 The manufacturing method of the composition of this invention is not specifically limited, It prepares by a conventional method. For example, the said components (a)-(d) Furthermore, the method of preparing by adding the said arbitrary component as needed and mixing this is mentioned.
本発明の組成物は、液状、ジェル状、クリーム状、固形状、ムース状等の種々の形態で実施することが可能であり、霧状に噴霧可能な容器に収容して霧状に噴霧して用いてもよい。また、本発明品の剤型は、可溶化型、水中油型、油中水型、油性型、水中油中水型、油中水中油型、多層型等特に限定されるものではない。 The composition of the present invention can be implemented in various forms such as liquid, gel, cream, solid, mousse, etc., and is stored in a sprayable container and sprayed in a mist. May be used. The dosage form of the product of the present invention is not particularly limited, such as a solubilizing type, an oil-in-water type, a water-in-oil type, an oily type, a water-in-oil-in-water type, an oil-in-water-in-oil type, and a multilayer type.
本発明の組成物の用途に関しては特に制限はなく、化粧料、皮膚外用剤、食品、インク、洗剤、衣料用柔軟仕上剤、芳香剤、消臭剤、織物等種々の用途の組成物として用いることができる。本発明の組成物は、老化防止効果等に優れるという観点から、化粧料又は皮膚外用剤として用いることが好ましい。 There is no restriction | limiting in particular regarding the use of the composition of this invention, It uses as a composition for various uses, such as cosmetics, an external preparation for skin, foodstuffs, ink, detergent, the softening finishing agent for clothes, a fragrance | flavor, a deodorant, and a textile. be able to. The composition of the present invention is preferably used as a cosmetic or a skin external preparation from the viewpoint of excellent anti-aging effect and the like.
本発明の食品(動物飼料を含む)の例としては、冷凍食品、粉末食品、シート状食品、瓶詰食品、缶詰食品、レトルト食品、カプセル状食品、タブレット状食品等の形態の他、例えば蛋白質、糖類、脂肪、微量元素、ビタミン類、乳化剤、香料等が含有された自然流動食、半消化栄養食および成分栄養食、ドリンク剤等の加工形態等、いずれの形態でもよい。 Examples of the food (including animal feed) of the present invention include frozen food, powdered food, sheet food, bottled food, canned food, retort food, capsule food, tablet food, etc. It may be in any form, such as natural liquid foods containing sugars, fats, trace elements, vitamins, emulsifiers, fragrances, etc., processed forms such as semi-digested nutrient foods and component nutrient foods, and drinks.
本発明の化粧料の例としては、特に限定されず、例えば、乳液、クリーム、化粧水、美容液、パック等のスキンケア化粧料、ファンデーション、頬紅、口紅、アイカラー、マスカラ、アイライナー、マニキュア等のメーキャップ化粧料、養毛料、ヘアトニック、シャンプー、リンス、ヘアワックス等の頭髪用化粧料、洗顔料等の洗浄料、等のいずれの形態であってもよい。 Examples of the cosmetics of the present invention are not particularly limited. For example, skin care cosmetics such as milky lotion, cream, lotion, cosmetic liquid, pack, foundation, blusher, lipstick, eye color, mascara, eyeliner, nail polish, etc. It may be in any form of makeup cosmetics, hair nourishing agents, hair tonics, shampoos, rinses, hair waxes and other cosmetics for hair, and facial cleansers.
本発明の皮膚外用剤の例としては、特に限定されず、例えば、外用ゲル剤、クリーム剤、軟膏剤、液剤、リニメント剤、ハップ剤等のいずれの形態であってもよい。 Examples of the external preparation for skin of the present invention are not particularly limited, and may be any form such as an external gel, cream, ointment, liquid, liniment, and haptic.
また、アスタキサンチン等のカロテノイドは、上述のとおり、有用な効果を有するものの、構造的に不安定であるため期待する効果を得難く、またその効果を長期にわたって維持しにくい。しかしながら、後記実施例に示すように、カロテノイド含有の組成物に、前記イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤を含有することで、組成物中のカロテノイドの安定化を図ることができる。 Moreover, although carotenoids such as astaxanthin have a useful effect as described above, it is difficult to obtain the expected effect due to structural instability, and it is difficult to maintain the effect over a long period of time. However, as shown in the Examples below, the carotenoid-containing composition is composed of one or more plants selected from the Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Asteraceae, Asteraceae, Simondiaceae, Acateaceae. By containing the obtained oil agent, the carotenoid in the composition can be stabilized.
本発明の前記イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤を利用することにより、カロテノイドの安定性を向上させることが可能となり、これによりカロテノイドの効能を有効に発揮させることができる。例えば、前記イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤は、カロテノイドの光による褪色の防止、光劣化抑制に著しい効果を発揮することができる。そして、カロテノイドは、肌荒れやシワの予防、改善、シミの予防、改善に有用であり、さらに老化防止や美白に有用であるので、前記イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤は、カロテノイドの持つこれら効果(例えば、老化防止効果や美白効果)を飛躍的に高めることができる。前記イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤を用いることで、より長期にわたってカロテノイドの効果を維持することができる、又は、カロテノイドの含有量を減らしても同等以上の効果を期待することができる。 By utilizing an oil agent obtained from one or more kinds of plants selected from the aforementioned Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Compositaeaceae, Spiraceae, Simondiaceae, and Acetaceae of the present invention, the stability of carotenoids is improved. It is possible to improve the efficiency of carotenoids. For example, the oil agent obtained from one or more plants selected from the Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Asteraceae, Moleaceae, Simondiaceae, and Acetaceae is used to prevent carotenoids from fading and photodegradation. It is possible to exert a remarkable effect on suppression. And carotenoids are useful for preventing and improving rough skin and wrinkles, preventing and improving stains, and also useful for preventing aging and whitening, so the gramineae, perilla, sesame, camellia, asteraceae, Oils obtained from one or more kinds of plants selected from the family Moleaceae, Simondiaceae, and Acanthaceae can dramatically enhance these effects (for example, anti-aging effect and whitening effect) possessed by carotenoids. Maintaining the effects of carotenoids over a longer period by using an oil agent obtained from one or more plants selected from the grass family, Lamiaceae, sesame family, camellia family, asteraceae family, oleaceae family, Simondiaceae family, Acetaceae family Even if the carotenoid content is reduced, the same or higher effect can be expected.
従って、本発明の前記イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤は、カロテノイドの安定化作用を有するため、前記イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤を有効成分とするカロテノイド安定化剤として使用することが可能である。本発明の前記イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤は、カロテノイドの安定化のために使用してもよく、またカロテノイド安定化の使用を目的とした各種製剤に使用することができ、これら各種製剤を製造するために使用することも可能である。よって、本発明のイネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤は、カロテノイドの安定化のために、皮膚外用剤、化粧料、医薬品、医薬部外品、飲食品や機能性食品(例えば特定保健用食品、サプリメント等)に含有することが可能である。本発明の前記イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤の使用量は、特に限定されないが、カロテノイド1質量部に対して、好ましくは1〜50000000質量部、より好ましくは1〜3000000質量部、特に好ましくは1〜2000000である。 Therefore, the oil agent obtained from one or more kinds of plants selected from the Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Asteraceae, Asteraceae, Simondiaceae, Acetaceae of the present invention has a carotenoid stabilizing effect. Therefore, it is used as a carotenoid stabilizer comprising as an active ingredient an oil agent obtained from one or more kinds of plants selected from the aforementioned gramineae, persimmonaceae, sesameaceae, camelliaceae, asteraceae, oleaceae, simoniaceae, and acetaceae. It is possible. The oil of the present invention obtained from one or more plants selected from the family Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Asteraceae, Oxaliaceae, Simondiaceae and Acetaceae is used for stabilizing carotenoids. It can also be used in various formulations intended for carotenoid stabilization and can be used to produce these various formulations. Therefore, the oil agent obtained from one or more plants selected from the family Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Asteraceae, Spiraceae, Simondiaceae, Acetaceae of the present invention is for stabilizing carotenoids. It can be contained in external preparations for skin, cosmetics, pharmaceuticals, quasi drugs, foods and drinks, and functional foods (for example, foods for specified health use, supplements, etc.). The amount of the oil agent obtained from one or more kinds of plants selected from the Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Compositaeaceae, Oleaceae, Simondiaceae, and Acetaceae of the present invention is not particularly limited, but carotenoid Preferably it is 1-50 million mass parts with respect to 1 mass part, More preferably, it is 1-3000 mass parts, Most preferably, it is 1-2 million.
以下、実施例を挙げて本発明をさらに具体的に説明するが、本発明の範囲はこれらに限定されるものではない。 Hereinafter, the present invention will be described more specifically with reference to examples, but the scope of the present invention is not limited thereto.
<アスタキサンチンの光安定化効果試験> <Photostabilization test of astaxanthin>
アスタキサンチンは波長470nmに特有の光吸収を有しており、アスタキサンチンの劣化が生じた場合には波長470nmの光吸収が減少するという性質を利用して、以下の手順に従ってアスタキサンチンの残存率を算出した。結果を表1に示した。
表1に示した各試料溶液を96ウェルプレートに200μl分注し、紫外線(UVB露光量:1.65J/cm2)を照射した。
Astaxanthin has light absorption peculiar to a wavelength of 470 nm, and when the degradation of astaxanthin occurs, the residual ratio of astaxanthin was calculated according to the following procedure using the property that light absorption at a wavelength of 470 nm decreases. . The results are shown in Table 1.
200 μl of each sample solution shown in Table 1 was dispensed into a 96-well plate and irradiated with ultraviolet rays (UVB exposure: 1.65 J / cm 2).
アスタキサンチン残存率は各試料溶液の470nmでの吸光度を測定し、下記式(1)を用いて算出した。ここで、アスタキサンチン含有系とは、アスタキサンチンを含有する実施例、参考例及び比較例を指し、アスタキサンチン非含有系とは、それぞれの実施例、参考例及び比較例中のアスタキサンチン5%溶液(アスタキサンチン−5C(オリザ油化社製))を、トリ(カプリル・カプリン酸)グリセリルに代えて調製したものを指す。
アスタキサンチン残存率(%)=((A−B)/(C−D))×100・・・(1)
A=紫外線照射アスタキサンチン含有系の吸光度
B=紫外線照射アスタキサンチン非含有系の吸光度
C=紫外線未照射アスタキサンチン含有系の吸光度
D=紫外線未照射アスタキサンチン非含有系の吸光度
The astaxanthin residual rate was calculated by measuring the absorbance at 470 nm of each sample solution and using the following formula (1). Here, the astaxanthin-containing system refers to Examples, Reference Examples and Comparative Examples containing astaxanthin, and the astaxanthin-free system refers to an astaxanthin 5% solution (astaxanthin − in each of Examples, Reference Examples and Comparative Examples). 5C (manufactured by Oriza Oil Chemical Co., Ltd.)) is referred to instead of tri (capryl / capric acid) glyceryl.
Astaxanthin residual rate (%) = ((A−B) / (C−D)) × 100 (1)
A = absorbance of an astaxanthin-containing system irradiated with ultraviolet light B = absorbance of an astaxanthin-free system irradiated with ultraviolet C = absorbance of an astaxanthin-containing system not irradiated with ultraviolet light D = absorbance of an astaxanthin-free system not irradiated with ultraviolet light
表1の結果より、参考例1〜8は、成分(b)のかわりに、トリ(カプリル・カプリン酸)グリセリル(MファインオイルCCT−1:ミヨシ油脂社製)を用いた参考例9に比べて、いずれもアスタキサンチンの光安定化効果に優れるものであった。 From the results in Table 1, Reference Examples 1 to 8 were compared to Reference Example 9 using tri (capryl / capric acid) glyceryl (M Fine Oil CCT-1: manufactured by Miyoshi Oil & Fats Co., Ltd.) instead of component (b). All of them were excellent in the photostabilization effect of astaxanthin.
<ニコチン酸アミド含有時におけるアスタキサンチン光安定化効果試験> <Astaxanthin light stabilization effect test when nicotinamide is contained>
本発明者らは、アスタキサンチン等のカロテノイドとニコチン酸アミドを組み合わせることにより、アスタキサンチン等のカロテノイドの光による褪色が促進されること(比較例1)、さらにその褪色促進は特定の植物から得られる油剤において抑制可能であることを見出した。その結果を表2に示す。 By combining carotenoids such as astaxanthin with nicotinic acid amide, the present inventors can promote the fading of carotenoids such as astaxanthin by light (Comparative Example 1), and further the fading promotion is an oil agent obtained from a specific plant. It was found that it can be suppressed. The results are shown in Table 2.
表2に示した各試料溶液を96ウェルプレートに200μl分注し、紫外線(UVB露光量:1.65J/cm2)を照射した。なお、アスタキサンチン残存率は、実施例1〜8と同様の方法にて測定した。 200 μl of each sample solution shown in Table 2 was dispensed into a 96-well plate and irradiated with ultraviolet rays (UVB exposure: 1.65 J / cm 2). In addition, the astaxanthin residual rate was measured by the method similar to Examples 1-8.
表2の結果より、驚くべきことに、成分(c)を含有しない参考例9よりも、成分(c)を含有する比較例1の方がアスタキサンチンの褪色が促進しており、成分(c)によるアスタキサンチンへの安定性上の影響がある事が示唆される。
一方、実施例1〜10は、成分(c)を配合しながらもアスタキサンチンの顕著な褪色が観察されず、成分(b)のかわりに、トリ(カプリル・カプリン酸)グリセリル(MファインオイルCCT−1:ミヨシ油脂社製)を用いた比較例1に比べて、表1の参考例1〜8の結果同様にいずれもアスタキサンチンの光安定化効果に優れるものであった。
From the results of Table 2, surprisingly, the discoloration of astaxanthin is promoted more in Comparative Example 1 containing component (c) than in Reference Example 9 not containing component (c), and component (c) It is suggested that there is an effect on the stability of astaxanthin by.
On the other hand, in Examples 1 to 10, no significant discoloration of astaxanthin was observed while compounding component (c), and instead of component (b), tri (capryl / capric acid) glyceryl (M fine oil CCT- 1: Compared to Comparative Example 1 using Miyoshi Oil & Fats Co., Ltd., all of the results of Reference Examples 1 to 8 in Table 1 were excellent in the light stabilization effect of astaxanthin.
実施例11[化粧水]
(成分) (%)
1.グリセリン 5.0
2.1,3−ブチレングリコール 5.0
3.乳酸 0.05
4. ニコチン酸アミド(注13) 2.5
5.乳酸ナトリウム 0.1
6.モノオレイン酸ポリオキシエチレン(20モル)ソルビタン 1.2
7.エタノール 8.0
8.コメ胚芽油(注2) 0.1
9.アスタキサンチン5%溶液(注14) 0.001
10.パラオキシ安息香酸メチル 0.1
11.香料 0.05
12.精製水 残 量
(注14)Astax−S (マリン大王社製)
Example 11 [skin lotion]
(Ingredient) (%)
1. Glycerin 5.0
2. 1,3-butylene glycol 5.0
3. Lactic acid 0.05
4. Nicotinamide (Note 13) 2.5
5). Sodium lactate 0.1
6). Polyoxyethylene monooleate (20 mol) sorbitan 1.2
7). Ethanol 8.0
8). Rice germ oil (Note 2) 0.1
9. Astaxanthin 5% solution (Note 14) 0.001
10. Methyl paraoxybenzoate 0.1
11. Fragrance 0.05
12 Purified water remaining amount (Note 14) Astax-S (manufactured by Marine Daio)
(製造方法)
A:成分(6)〜(11)を混合溶解する。
B:成分(1)〜(5)及び(12)を混合溶解する。
C:BにAを添加混合し、化粧水を得た。
(Production method)
A: Components (6) to (11) are mixed and dissolved.
B: Components (1) to (5) and (12) are mixed and dissolved.
C: A was added to B and mixed to obtain a skin lotion.
実施例11の化粧水は、アスタキサンチン類の安定化効果に優れたものであった。 The lotion of Example 11 was excellent in the stabilization effect of astaxanthins.
実施例12[乳液]
(成分) (%)
1.モノステアリン酸ポリオキシエチレン(20モル)ソルビタン 1.0
2.トリオレイン酸ポリオキシエチレン(20モル)ソルビタン 0.5
3.グリセリルモノステアレート 1.0
4.コメヌカ油(注3) 1.0
5.ステアリン酸 0.5
6.ベヘニルアルコール 0.5
7.スクワラン 4.0
8.カルボキシビニルポリマー 0.1
9.パラオキシ安息香酸メチル 0.1
10.水酸化ナトリウム 0.05
11. ニコチン酸アミド(注13) 5.0
12.精製水 残 量
13.エタノール 5.0
14.アスタキサンチン5%溶液(注1) 0.01
15.香料 0.05
Example 12 [Emulsion]
(Ingredient) (%)
1. Polyoxyethylene monostearate (20 mol) sorbitan 1.0
2. Polyoxyethylene trioleate (20 mol) sorbitan 0.5
3. Glyceryl monostearate 1.0
4). Rice bran oil (Note 3) 1.0
5). Stearic acid 0.5
6). Behenyl alcohol 0.5
7). Squalane 4.0
8). Carboxyvinyl polymer 0.1
9. Methyl paraoxybenzoate 0.1
10. Sodium hydroxide 0.05
11. Nicotinamide (Note 13) 5.0
12 Purified water remaining amount 13. Ethanol 5.0
14 Astaxanthin 5% solution (Note 1) 0.01
15. Fragrance 0.05
(製造方法)
A:成分(1)〜(7)を70℃で均一に混合する。
B:成分(8)〜(12)を70℃で均一に混合する。
C:BにAを加えて乳化し、室温まで冷却する。
D:(13)〜(15)を加えて均一に混合し、乳液を得た。
(Production method)
A: Components (1) to (7) are uniformly mixed at 70 ° C.
B: Components (8) to (12) are uniformly mixed at 70 ° C.
C: A is added to B to emulsify, and cooled to room temperature.
D: (13) to (15) were added and mixed uniformly to obtain an emulsion.
実施例12の乳液は、アスタキサンチン類の安定化効果に優れたものであった。 The emulsion of Example 12 was excellent in the stabilization effect of astaxanthins.
実施例13[日焼け止め化粧料(油中水型クリーム状)]
(成分) (%)
1.モノラウリン酸ポリオキシエチレン(20モル)ソルビタン 0.2
2.ポリオキシエチレン(60モル)硬化ヒマシ油 0.1
3.精製水 残 量
4.ジプロピレングリコール 10.0
5.硫酸マグネシウム 0.5
6.アスコルビン酸グルコシド 2.0
7.ニコチン酸アミド(注13) 4.0
8.シリコーン化合物(注15) 3.0
9.デカメチルシクロペンタシロキサン 20.0
10.イソノナン酸イソトリデシル 5.0
11.パラメトキシケイ皮酸2−エチルヘキシル 8.0
12.オリーブ果実油(注7) 3.0
13.アスタキサンチン5%溶液(注16) 0.01
14.ジメチルステアリルアンモニウムヘクトライト 1.2
(注15)KF−6028 (信越化学工業社製)
(注16)アスタキサンチン5%オイル(バイオアクティブズジャパン社製)
Example 13 [sunscreen cosmetic (water-in-oil cream)]
(Ingredient) (%)
1. Polyoxyethylene monolaurate (20 mol) sorbitan 0.2
2. Polyoxyethylene (60 mol) hydrogenated castor oil 0.1
3. Residual amount of purified water 4. Dipropylene glycol 10.0
5). Magnesium sulfate 0.5
6). Ascorbic acid glucoside 2.0
7). Nicotinamide (Note 13) 4.0
8). Silicone compound (Note 15) 3.0
9. Decamethylcyclopentasiloxane 20.0
10. Isotridecyl isononanoate 5.0
11. 2-Ethylhexyl paramethoxycinnamate 8.0
12 Olive fruit oil (Note 7) 3.0
13. Astaxanthin 5% solution (Note 16) 0.01
14 Dimethylstearyl ammonium hectorite 1.2
(Note 15) KF-6028 (Shin-Etsu Chemical Co., Ltd.)
(Note 16) Astaxanthin 5% oil (manufactured by Bioactives Japan)
(製造方法)
A:成分(1)〜(7)を均一に分散する。
B:成分(8)〜(14)を均一に分散する。
C:Bを攪拌しながら徐々にAを加えて乳化し、油中水型クリーム状日焼け止め化粧料を得た。
(Production method)
A: Components (1) to (7) are uniformly dispersed.
B: Components (8) to (14) are uniformly dispersed.
C: While stirring B, A was gradually added to emulsify to obtain a water-in-oil cream sunscreen cosmetic.
実施例13の日焼け止め化粧料(油中水型クリーム状)は、アスタキサンチン類の安定化効果に優れたものであった。 The sunscreen cosmetic of Example 13 (water-in-oil cream) was excellent in the astaxanthin stabilizing effect.
実施例14[軟膏剤]
(成分) (%)
1.トリエタノールアミン 2.0
2.グリセリン 5.0
3.グリチルリチン酸ジカリウム 0.5
4.精製水 残 量
5.ニコチン酸アミド(注13) 6.0
6.ステアリン酸 18.0
7.セタノール 4.0
8.ホホバ油(注8) 0.5
9.アスタキサンチン5%溶液(注1) 0.01
10.酢酸dl−α―トコフェロール 0.2
11.パラオキシ安息香酸メチル 0.1
Example 14 [Ointment]
(Ingredient) (%)
1. Triethanolamine 2.0
2. Glycerin 5.0
3. Dipotassium glycyrrhizinate 0.5
4). 4. Purified water balance Nicotinamide (Note 13) 6.0
6). Stearic acid 18.0
7). Cetanol 4.0
8). Jojoba oil (Note 8) 0.5
9. Astaxanthin 5% solution (Note 1) 0.01
10. Dl-α-tocopherol acetate 0.2
11. Methyl paraoxybenzoate 0.1
(製造方法)
A.成分(1)〜(5)を均一溶解し、75℃に保つ。
B.成分(6)〜(11)を加熱混合し、75℃に保つ。
C.AにBを徐々に加え、軟膏剤を得た。
(Production method)
A. Ingredients (1) to (5) are uniformly dissolved and kept at 75 ° C.
B. Ingredients (6) to (11) are heated and mixed and maintained at 75 ° C.
C. B was gradually added to A to obtain an ointment.
実施例14の軟膏剤は、アスタキサンチン類の安定化効果に優れたものであった。
The ointment of Example 14 was excellent in the stabilization effect of astaxanthins.
本発明のアスタキサンチン類等のカロテノイドの安定化方法は、飲食品や組成物に配合することが可能であり、老化防止、シミ、シワの予防・改善等の肌への効果を発揮するのに有用である。 The method for stabilizing carotenoids such as astaxanthins of the present invention can be blended in foods and drinks and compositions, and is useful for exerting skin effects such as anti-aging, prevention of wrinkles and wrinkles. It is.
Claims (8)
(a)カロテノイド
(b)イネ科、シソ科、ゴマ科、ツバキ科、キク科、モクセイ科、シモンジア科、アカテツ科から選ばれる1種以上の植物から得られる油剤
(c)ニコチン酸アミド
を含有する組成物。 The following components (a) to (c);
(A) Carotenoid (b) Contains oil agent (c) nicotinic acid amide obtained from one or more plants selected from the family Gramineae, Lamiaceae, Sesameaceae, Camelliaaceae, Asteraceae, Spiraceae, Simondiaceae, Acetaceae Composition.
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011032171A (en) * | 2009-07-29 | 2011-02-17 | Fuji Chem Ind Co Ltd | Skin whitening composition |
JP2014156456A (en) * | 2013-01-21 | 2014-08-28 | Fujifilm Corp | External preparation for skin |
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2011032171A (en) * | 2009-07-29 | 2011-02-17 | Fuji Chem Ind Co Ltd | Skin whitening composition |
JP2014156456A (en) * | 2013-01-21 | 2014-08-28 | Fujifilm Corp | External preparation for skin |
Non-Patent Citations (1)
Title |
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VITAMIN C ESTER EYE SERUM,ID 1173979,MINTEL GNPD[ONLINE],2009年9月,[検索日2022.12.22],URL,HTTPS, JPN6022055016, ISSN: 0004955370 * |
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