JP2007063177A - Composition for oral intake intended for lustrous skin - Google Patents

Composition for oral intake intended for lustrous skin Download PDF

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JP2007063177A
JP2007063177A JP2005250453A JP2005250453A JP2007063177A JP 2007063177 A JP2007063177 A JP 2007063177A JP 2005250453 A JP2005250453 A JP 2005250453A JP 2005250453 A JP2005250453 A JP 2005250453A JP 2007063177 A JP2007063177 A JP 2007063177A
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skin
composition
ascorbic acid
wrinkles
hyaluronic acid
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JP4982718B2 (en
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Shigeharu Fukuda
恵温 福田
Toshio Miyake
俊雄 三宅
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Hayashibara Seibutsu Kagaku Kenkyujo KK
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Hayashibara Biochemical Laboratories Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a composition for oral intake which is capable of attaining ameliorating skin flabbiness, wrinkles and/or fine wrinkles and rough skin and improving skin moisture. <P>SOLUTION: The composition for oral intake is such that the compounding mass ratio of hyaluronic acid to an L-ascorbic acid compound on an L-ascorbic acid basis is (1:4) to (4:1). <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

本発明は、肌の弛み、シワ及び/又はコジワを改善する美肌用の経口摂取用組成物に関する。   The present invention relates to a composition for oral intake for beautifying skin that improves skin sag, wrinkles and / or wrinkles.

従来から、肌の弛み、シワ及びコジワを改善し、美しい肌を保つことは多くの人々が希望とするところであり、これらを目的とする種々の製品が開発されている。これらの製品は、一般には化粧品という形態で提供され皮膚に塗布されるものが多いが、他方においては経口的に摂取されることにより上記目的を達成しようとする製品もある。   Conventionally, many people have desired to improve skin slackness, wrinkles and wrinkles, and to keep beautiful skin, and various products for these purposes have been developed. Many of these products are generally provided in the form of cosmetics and applied to the skin. On the other hand, there are products that try to achieve the above-mentioned purpose by being taken orally.

ヒアルロン酸は、真皮層に多く存在し、皮膚の保湿性や弾力性に関与していることが知られている。そのため、皮膚の保湿性や弾力性の維持を目的にした、ヒアルロン酸を含有させた食品が幾つか開発されている(特許文献1、特許文献2参照)。   Hyaluronic acid is abundant in the dermis layer and is known to be involved in the moisture retention and elasticity of the skin. For this reason, several foods containing hyaluronic acid have been developed for the purpose of maintaining the moisture retention and elasticity of the skin (see Patent Document 1 and Patent Document 2).

L−アスコルビン酸類は、皮膚や粘膜の健康維持を助ける抗酸化ビタミンとして、或いは、抗酸化剤として経口摂取用の組成物に利用されている(特許文献3)。また、L−アスコルビン酸類は、メラニンの生成を抑制することから、美白用の化粧料にも使用されている(特許文献4)。また、L−アスコルビン酸類を利用した、コラーゲン産生増強用の組成物も提案されている(特許文献5)。しながら、特定の割合で、ヒアルロン酸とL−アスコルビン酸類とを経口的に摂取することにより、肌の弛み、シワ及び/又はコジワを改善する美肌効果が顕著に発揮されることについての報告はない。   L-ascorbic acids are used in compositions for oral intake as antioxidant vitamins that help maintain the health of skin and mucous membranes or as antioxidants (Patent Document 3). L-ascorbic acids are also used in whitening cosmetics because they suppress the production of melanin (Patent Document 4). A composition for enhancing collagen production using L-ascorbic acids has also been proposed (Patent Document 5). However, there is a report that the skin beautifying effect that improves skin slackness, wrinkles and / or wrinkles is remarkably exhibited by taking hyaluronic acid and L-ascorbic acid orally at a specific ratio Absent.

特開平10−165138号公報JP-A-10-165138 特開2005−80532号公報JP 2005-80532 A 特開2003−339353号公報JP 2003-339353 A 特開平3−139288号公報JP-A-3-139288

本発明は、肌の弛み、シワ及び/又はコジワを改善し、肌荒れの改善や肌のうるおいの向上を達成することができる経口摂取用の組成物を提供することを課題とする。   An object of the present invention is to provide a composition for oral intake that can improve skin looseness, wrinkles and / or wrinkles, and can achieve improvement of rough skin and improvement of moisture of the skin.

本発明者は、上記課題を解決するために、鋭意研究した結果、特定の割合でヒアルロン酸およびL−アスコルビン酸類を併せて経口的に摂取すると、効果的に美しい肌を保つことができることを見出し、本発明を完成した。すなわち、本発明は、ヒアルロン酸とL−アスコルビン酸に換算したときのL−アスコルビン酸類との配合割合が、質量比で1:4乃至4:1である経口摂取用組成物を提供することにより上記課題を解決するものである。   As a result of earnest research to solve the above problems, the present inventor has found that when hyaluronic acid and L-ascorbic acids are taken orally in a specific ratio, beautiful skin can be effectively maintained. The present invention has been completed. That is, the present invention provides a composition for oral consumption in which the blending ratio of hyaluronic acid and L-ascorbic acid when converted to L-ascorbic acid is 1: 4 to 4: 1 by mass ratio. The present invention solves the above problems.

本発明の経口摂取用組成物は経口摂取することにより、摂取した者の、肌の弛み、シワ及び/又はコジワを改善すると共に、角層のバリア機能を改善し、皮膚の保水力を高め、肌荒れの改善、肌のうるおいが向上し、美しい肌が保持される。   The composition for oral ingestion of the present invention, when orally ingested, improves the slackness, wrinkles and / or wrinkles of the ingested person, improves the barrier function of the stratum corneum, and enhances the water retention capacity of the skin, Improves rough skin, improves moisture and keeps beautiful skin.

本発明の経口摂取用組成物に使用するヒアルロン酸は、化学合成されたものでもよく、発酵法で製造したものや、動物の組織や微生物等から抽出したものであっても良い。ヒアルロン酸は、本発明の効果を妨げない限り、必ずしも精製または単離されたものを用いる必要はなく、未分離組成物としての形態、それらを部分精製、或いは、高度に精製したものであってもよい。また、本発明の経口摂取用組成物に含まれるヒアルロン酸は、その少なくとも一部がヒアルロン酸ナトリウムなどの塩の形態になっていてもよい。   The hyaluronic acid used in the composition for oral ingestion of the present invention may be chemically synthesized, may be produced by fermentation, or may be extracted from animal tissues or microorganisms. Hyaluronic acid does not necessarily need to be purified or isolated as long as it does not interfere with the effects of the present invention, and is in the form of an unseparated composition, partially purified or highly purified. Also good. Moreover, at least a part of the hyaluronic acid contained in the composition for oral consumption of the present invention may be in the form of a salt such as sodium hyaluronate.

本発明の経口摂取用組成物に含まれるヒアルロン酸の含有量は、特に制限はなく、通常は、該組成物全質量に対して0.1質量%乃至25質量%であることが好ましい。   There is no restriction | limiting in particular in content of the hyaluronic acid contained in the composition for oral intake of this invention, Usually, it is preferable that it is 0.1 mass% thru | or 25 mass% with respect to this composition total mass.

本発明で使用するL−アスコルビン酸類としては、経口摂取が可能で、生体内において、ビタミンCとしての生理機能を発揮できるものであれば、特に限定されない。具体的には、例えば、L−アスコルビン酸や、L−アスコルビン酸配糖体、L−アスコルビン酸脂肪酸エステル、L−アスコルビン酸リン酸エステルなどのL−アスコルビン酸の誘導体、ニコチン酸アミド−Lアスコルビン酸複合体、これらL−アスコルビン酸類のアルカリ金属塩又はアルカリ土類金属塩の他、アンモニウム塩、アミノ酸塩等の塩も同様に使用することができる。なかでも、L−アスコルビン酸配糖体の1種であるL−アスコルビン酸2−グルコシドは、経口摂取用組成物に配合しても安定であるばかりでなく、経口摂取すると、生体内で徐々に分解されて、持続的にビタミンC作用を発揮し、ヒアルロン酸と組み合わせた場合には、他のL−アスコルビン酸類に比して、強い美肌作用を持続することができるので、特に望ましい。   The L-ascorbic acid used in the present invention is not particularly limited as long as it can be taken orally and can exhibit physiological functions as vitamin C in vivo. Specifically, for example, L-ascorbic acid, L-ascorbic acid glycosides, L-ascorbic acid fatty acid esters, L-ascorbic acid phosphates and other derivatives of L-ascorbic acid, nicotinamide-L ascorbine In addition to acid complexes and alkali metal salts or alkaline earth metal salts of these L-ascorbic acids, salts such as ammonium salts and amino acid salts can also be used. Among them, L-ascorbic acid 2-glucoside, which is one of L-ascorbic acid glycosides, is not only stable even when blended in an oral intake composition, but gradually in vivo when ingested. When it is decomposed and continuously exerts vitamin C action and is combined with hyaluronic acid, it is particularly desirable because it can maintain a strong skin beautifying action compared to other L-ascorbic acids.

本発明の経口摂取用組成物に含まれるL−アスコルビン酸類の含有量は、特に制限はなく、通常は、L−アスコルビン酸に換算して、該組成物全質量に対して0.1質量%乃至25質量%であることが好ましい。   The content of L-ascorbic acid contained in the composition for oral consumption of the present invention is not particularly limited, and is usually 0.1% by mass in terms of the total mass of the composition in terms of L-ascorbic acid. It is preferable that it is thru | or 25 mass%.

本発明の経口摂取用組成物におけるヒアルロン酸とL−アスコルビン酸類との配合割合は、本発明の所期の作用効果が達成できればよく、ヒアルロン酸とL−アスコルビン酸に換算したときのL−アスコルビン酸類との配合割合が、質量比で1:4乃至4:1、望ましくは1:2乃至2:1のものが、美肌効果の点で優れている。   The blending ratio of hyaluronic acid and L-ascorbic acid in the composition for oral consumption of the present invention is only required to achieve the intended effect of the present invention. L-ascorbine when converted to hyaluronic acid and L-ascorbic acid A compounding ratio with acids is 1: 4 to 4: 1, preferably 1: 2 to 2: 1 in terms of mass ratio, which is excellent in terms of skin beautifying effect.

また、このヒアルロン酸とL−アスコルビン酸類との経口摂取は、これらの2成分を含む組成物を摂取することが望ましいが、ヒアルロン酸とL−アスコルビン酸に換算したときのL−アスコルビン酸類との摂取割合が、質量比で1:4乃至4:1となるように、各々の成分を、別々に経口摂取する場合も、本発明に含まれる。   Moreover, although it is desirable to ingest these hyaluronic acid and L-ascorbic acids with a composition containing these two components, the hyaluronic acid and the L-ascorbic acids when converted to L-ascorbic acid are preferable. The case where each component is orally ingested separately so that the ingestion ratio is 1: 4 to 4: 1 by mass ratio is also included in the present invention.

本発明の経口摂取物組成物の成人1日当たりの摂取量は、所期の作用効果が達成できる限り、特に制限はないが、通常は、ヒアルロン酸の摂取量及びL−アスコルビン酸に換算したときのL−アスコルビン酸類の摂取量は、何れも、1日当たり60mg以上とするのが望ましく、90mg以上が好適であり、120mg以上とするのが特に望ましい。   The daily intake of the oral ingestion composition of the present invention is not particularly limited as long as the desired effect can be achieved, but usually when converted into hyaluronic acid intake and L-ascorbic acid In any case, the intake of L-ascorbic acid is preferably 60 mg or more, more preferably 90 mg or more, and particularly preferably 120 mg or more.

本発明の経口摂取用組成物は、本発明の作用効果を妨げない範囲で、ヒアルロン酸及びL−アスコルビン酸類以外の、通常経口摂取用組成物に加えられる成分を任意に含有させることができる。例えば、ブドウ糖、果糖、グルコサミン、ラクトース、蔗糖、α,α−トレハロース、α,β−トレハロース、β,β−トレハロース、ラクトスクロース、マルトオリゴ糖、水飴などの糖類、サイクロデキストリンや同じ出願人による国際公開WO 02/10361号明細書などに記載のサイクロ{→6)−α−D−グルコピラノシル−(1→3)−α−D−グルコピラノシル−(1→6)−α−D−グルコピラノシル−(1→3)−α−D−グルコピラノシル−(1→}の構造を有する環状四糖、或いは、特開2005−95148号公報(特願2004−174880号明細書)などに記載のサイクロ{→6)−α−D−グルコピラノシル−(1→4)−α−D−グルコピラノシル−(1→6)−α−D−グルコピラノシル−(1→4)−α−D−グルコピラノシル−(1→}の構造を有する環状四糖などの環状の糖類、エリスリトール、マンニトール、ソルビトール、キシリトール、マルチトール、還元水飴などの糖アルコール類、アスパルテーム、ステビア抽出物、スクラロース、アセスルファムKなどの高甘味度甘味料、プルラン、カラギーナン、コンドロイチン硫酸などのムコ多糖体やその塩類、天然ガム類、キチン、キトサン、カルボキシメチルセルロースをはじめとする合成高分子ポリマー、コラーゲン、ゼラチンなどの増粘剤の何れか1種又は2種以上を添加することができる。なかでも、コンドロイチン硫酸やグルコサミンを併用することにより、本発明の経口摂取用組成物の美肌効果を、より増強することができる。   The composition for oral ingestion of the present invention can optionally contain components that are usually added to the composition for oral ingestion other than hyaluronic acid and L-ascorbic acids, as long as the effects of the present invention are not hindered. For example, sugars such as glucose, fructose, glucosamine, lactose, sucrose, α, α-trehalose, α, β-trehalose, β, β-trehalose, lactosucrose, maltooligosaccharide, varicella, cyclodextrin and international publication by the same applicant Cyclo {→ 6) -α-D-glucopyranosyl- (1 → 3) -α-D-glucopyranosyl- (1 → 6) -α-D-glucopyranosyl- (1 →) described in WO 02/10361 3) Cyclic tetrasaccharide having a structure of -α-D-glucopyranosyl- (1 →) or cyclo {→ 6)-described in JP-A-2005-95148 (Japanese Patent Application No. 2004-174880) etc. α-D-glucopyranosyl- (1 → 4) -α-D-glucopyranosyl- (1 → 6) -α-D-glucopyranosyl- (1 → 4) -α-D Cyclic sugars such as cyclic tetrasaccharides having the structure of glucopyranosyl- (1 →}, sugar alcohols such as erythritol, mannitol, sorbitol, xylitol, maltitol, reduced starch syrup, aspartame, stevia extract, sucralose, acesulfame K, etc. High-intensity sweeteners, mucopolysaccharides such as pullulan, carrageenan, chondroitin sulfate and their salts, natural gums, chitin, chitosan, synthetic polymer polymers such as carboxymethylcellulose, thickeners such as collagen and gelatin In particular, the skin beautifying effect of the composition for oral consumption of the present invention can be further enhanced by using chondroitin sulfate or glucosamine in combination.

また、本発明の経口摂取用組成物には、上記以外にも、例えば、ビタミンB、ビタミンB、ビタミンB、ビタミンB12、ビタミンE、ルチン・ヘスペリジン・ナリンジンなどのバイオフラボノイド類或いは、これらビタミンやフラボノイドの誘導体など、アミノ酸類、CoQ10(コエンザイムQ10)、アデノシンやその誘導体、それらのモノフォスフェイト、ジフォスフェイト或いはトリフォスフェイトのような核酸関連物質、プロポリス、フラボノイド類などの成分、海洋深層水などのミネラル類、賦形剤、結合剤、被覆剤、滑沢剤、崩壊剤、増量剤、抗酸化剤、矯味矯臭剤、呈味剤、乳化・可溶化・分散剤、安定剤、pH調節剤、着色料、香料、甘味料、酸味料などから選ばれる何れか1種又は2種以上を含有させることも随意である。 In addition to the above, the composition for oral consumption of the present invention includes, for example, bioflavonoids such as vitamin B 1 , vitamin B 2 , vitamin B 6 , vitamin B 12 , vitamin E, rutin, hesperidin, naringin, etc. , Amino acids such as vitamins and flavonoid derivatives, CoQ10 (coenzyme Q10), adenosine and derivatives thereof, nucleic acid related substances such as monophosphate, diphosphate or triphosphate, propolis, flavonoids, and other components , Minerals such as deep sea water, excipients, binders, coating agents, lubricants, disintegrants, extenders, antioxidants, flavoring agents, flavoring agents, emulsifying / solubilizing / dispersing agents, stability Any one or more selected from agents, pH adjusters, colorants, flavors, sweeteners, acidulants, etc. And it is also optional.

本発明の経口摂取用組成物は、ヒアルロン酸及びL−アスコルビン酸類を、該組成物が完成するまでの工程で、或いは、完成品に対して、含有せしめればよく、その具体的な方法としては、例えば、混和、混捏、溶解、融解、分散、懸濁、乳化、浸透、晶出、散布、塗布、付着、噴霧、被覆(コーティング)、注入、浸漬、固化、逆ミセル化などの、飲食品の製造に使用することのできる1種又は2種以上の方法の組み合わせが適宜に選ばれる。   The composition for oral ingestion of the present invention may contain hyaluronic acid and L-ascorbic acid in the process until the composition is completed or in the finished product. For example, mixing, kneading, dissolving, melting, dispersing, suspending, emulsifying, penetrating, crystallization, spraying, applying, adhering, spraying, coating (coating), pouring, dipping, solidifying, reverse micelle, etc. One or a combination of two or more methods that can be used for the production of the product is appropriately selected.

本発明の経口摂取用組成物は、その形状を問わず、例えば、液状、シラップ、マスキット、ペースト、粉末、固状、半固状、顆粒、錠剤、ゲルなどの何れの形状であってもよく、そのままで、又は、必要に応じて、増量剤、賦形剤、結合剤などと混合して、液剤、乳剤、懸濁剤、シラップ剤、ペースト、顆粒剤、粉末剤、錠剤、カプセル剤など各種剤型で使用することもできる。   The composition for oral consumption of the present invention may be in any shape, for example, liquid, syrup, muskit, paste, powder, solid, semi-solid, granule, tablet, gel, etc. , As is, or mixed with bulking agents, excipients, binders, etc. as necessary, as liquids, emulsions, suspensions, syrups, pastes, granules, powders, tablets, capsules, etc. It can also be used in various dosage forms.

以下、実験例により本発明をさらに詳細に説明する。   Hereinafter, the present invention will be described in more detail with reference to experimental examples.

<実験例1:ヒアルロン酸及び/又はL−アスコルビン酸類の経口摂取の肌に及ぼす影響>
ヒアルロン酸及び/又はL−アスコルビン酸類の経口摂取の肌に及ぼす影響を調べる試験を以下のように行った。すなわち、ヒアルロン酸と、L−アスコルビン酸、L−アスコルビン酸2−グルコシド(株式会社林原商事販売、商品名「アスコフレッシュ」)、L−アスコルビン酸脂肪酸エステル、滑潤剤としてショ糖脂肪酸エステル、及び、賦形剤として精製マルトース(株式会社林原商事販売、商品名「サンマルトS」)を、表1に示す質量比で混合して、全量を10質量部として、これを常法により打錠して、各々0.3g/錠の錠剤を調製した。その各々の配合の錠剤につき、各々17名の被験者に、1日当たり6錠を、3ヶ月間経口摂取させた。各々の被験者について、肌の状態を、下記評価方法1乃至評価方法3を用いて評価し、その結果を表1に示す。なお、L−アスコルビン酸2−グルコシド及びL−アスコルビン酸脂肪酸エステルの配合量は、L−アスコルビン酸に換算した量を表1に示した。なお、陰性対照として、これらの錠剤を摂取しなかった被験者17名についても、同様に評価を行い、その結果を併せて表1に示す。
<評価方法1>
摂取前、摂取2ヵ月後及び3ヵ月後に頬の角層水分蒸散量をTEWAメーター(テヴァメーター)により測定した。配合例毎に被験者17名の頬からの角層水分蒸散量の平均値を求めた。
<評価方法2>
各々の被験者を、摂取前及び摂取3ヵ月後に、角層の重層剥離の程度について観察し、摂取前に比してどのような変化が認められたかを、5段階にスコア化した(1:減少した、2:少し減少した、3:変化無し、4:少し増加した、5:増加した)。各配合の錠剤を摂取した17名の被験者ごとにスコアの平均を求めた。
<評価方法3>
各々の被験者から、摂取3ヵ月後に肌のかさつきの程度と、肌の弛み、シワ及びコジワの変化についてのアンケート調査を行った。それぞれの項目に関して改善を自覚した者の割合を改善率とした。
<Experimental Example 1: Effect of oral intake of hyaluronic acid and / or L-ascorbic acid on skin>
A test for examining the effect of oral intake of hyaluronic acid and / or L-ascorbic acid on the skin was performed as follows. That is, hyaluronic acid, L-ascorbic acid, L-ascorbic acid 2-glucoside (sales by Hayashibara Corporation, trade name “ASCOFRESH”), L-ascorbic acid fatty acid ester, sucrose fatty acid ester as a lubricant, and Purified maltose (trade name “Sanmalto S”, sold by Hayashibara Co., Ltd.) as an excipient was mixed at a mass ratio shown in Table 1, and the total amount was 10 parts by mass. Each tablet was prepared at 0.3 g / tablet. For each tablet of each formulation, 17 subjects each took 6 tablets per day for 3 months. For each subject, the skin condition was evaluated using the following evaluation methods 1 to 3, and the results are shown in Table 1. In addition, the compounding quantity of L-ascorbic acid 2-glucoside and L-ascorbic acid fatty acid ester showed the quantity converted into L-ascorbic acid in Table 1. As a negative control, 17 subjects who did not take these tablets were similarly evaluated, and the results are shown in Table 1.
<Evaluation method 1>
Before ingestion, 2 months after ingestion and 3 months later, the amount of transpiration of the stratum corneum in the cheek was measured with a TEWA meter (Tevameter). The average value of the horny layer moisture transpiration from the cheeks of 17 subjects was determined for each formulation example.
<Evaluation method 2>
Each subject was observed for the degree of delamination of the stratum corneum before ingestion and after 3 months of ingestion, and the change observed compared to before ingestion was scored in 5 stages (1: decrease) 2: slightly decreased, 3: no change, 4: increased slightly, 5: increased). The average score was calculated for each of 17 subjects who took tablets of each formulation.
<Evaluation method 3>
Each subject conducted a questionnaire survey on the degree of skin roughness, skin looseness, wrinkles and changes in wrinkles 3 months after ingestion. The percentage of those who were aware of improvement in each item was taken as the improvement rate.

Figure 2007063177
Figure 2007063177

<結果>
表1から明らかなよう、ヒアルロン酸或いはL−アスコルビン酸類を単独で摂取した場合(配合No.1乃至配合No.4)には、頬からの水分蒸散量、角層の重層剥離の程度、肌のかさつきの程度、肌の弛み、シワ及びコジワを改善の程度の何れにおいても、摂取前に比して変化は認められなかった。これに対して、ヒアルロン酸とL−アスコルビン酸類を等質量配合した錠剤を摂取した場合(配合No.5乃至配合No.7)には、評価に使用した何れの項目においても、摂取前に比して改善が認められた。また、ヒアルロン酸と組み合わせるL−アスコルビン酸類としては、L−アスコルビン酸2−グルコシドを使用した場合に最も強い改善効果が認められた。
<Result>
As is clear from Table 1, when hyaluronic acid or L-ascorbic acid was ingested alone (Formulation No. 1 to No. 4), the amount of water transpiration from the cheeks, the degree of exfoliation of the stratum corneum, and the skin No change was observed in any of the degree of bulkiness, skin looseness, wrinkles and wrinkles to improve. On the other hand, when taking tablets containing equal amounts of hyaluronic acid and L-ascorbic acid (formulation No. 5 to No. 7), any of the items used for evaluation were compared with those before ingestion. Improvement was observed. Moreover, as L-ascorbic acid combined with hyaluronic acid, the strongest improvement effect was recognized when L-ascorbic acid 2-glucoside was used.

<実験例2:ヒアルロン酸及びL−アスコルビン酸類の摂取量の及ぼす肌への影響>
ヒアルロン酸及びL−アスコルビン酸類の摂取量の及ぼす肌への影響を調べる実験を以下のようにして行った。即ち、実験例1で調製した配合No.6のヒアルロン酸とL−アスコルビン酸2−グルコシドとを等質量配合した錠剤を使用して、1日当たり、1錠、2錠、3錠、4錠、5錠、或いは6錠の何れかを、各々17名の被験者に2ヶ月間摂取させた。各々の被験者について、実験終了時の、被験者の頬の皮膚の状態を、実験例1と同じ評価方法1乃至評価方法3を用いて評価し、その結果を表2に示す。なお、実験例2と実験例1とは、被験者が重複しないように実験を行った。
<Experimental Example 2: Effects on the skin of hyaluronic acid and L-ascorbic acid intake>
An experiment for examining the effect on the skin of the intake of hyaluronic acid and L-ascorbic acid was performed as follows. That is, the formulation No. prepared in Experimental Example 1 was obtained. 6 tablets of hyaluronic acid and L-ascorbic acid 2-glucoside in an equal mass are used, and one tablet, two tablets, three tablets, four tablets, five tablets, or six tablets per day, Each of 17 subjects ingested for 2 months. For each subject, the condition of the subject's cheek skin at the end of the experiment was evaluated using the same evaluation methods 1 to 3 as in Experimental Example 1, and the results are shown in Table 2. In addition, the experiment example 2 and the experiment example 1 were conducted so that the subjects did not overlap.

Figure 2007063177
Figure 2007063177

表2から明らかなように、錠剤を1日当たり1錠摂取した場合には、評価に使用した何れの項目においても、摂取前に比して改善は認められなかった。これに対して、1日当たり、2錠を摂取した場合には、評価に使用した何れの項目においても、摂取前に比して改善が認められ、その改善は、1日当たり3錠以上の摂取で顕著であった。   As is apparent from Table 2, when one tablet was taken per day, no improvement was observed in any of the items used for the evaluation as compared to before the intake. On the other hand, when taking 2 tablets per day, improvement was observed in all items used for evaluation compared to before taking, and the improvement was achieved by taking 3 tablets or more per day. It was remarkable.

<実験例3:経口摂取用組成物中のヒアルロン酸とL−アスコルビン酸類との配合割合の肌に及ぼす影響>
実験例1で、ヒアルロン酸とL−アスコルビン酸類とを組み合わせて経口摂取することにより、肌の弛み、シワ及びコジワが改善されることが確認されたので、経口摂取用組成物中のヒアルロン酸とL−アスコルビン酸類との配合割合の肌に及ぼす影響を調べる試験を以下のように行った。すなわち、ヒアルロン酸と、L−アスコルビン酸2−グルコシド(株式会社林原商事販売、商品名「アスコフレッシュ」)、ショ糖脂肪酸エステル、賦形剤として精製マルトース(株式会社林原商事販売、商品名「サンマルトS」)を表3に示す質量比で混合して、全量を10質量部とし、これを常法により打錠して、各々0.3g/錠の錠剤を調製した。その各々の配合につき、各々17名の被験者に、1日当たり6錠、3ヶ月間経口摂取させた。各々の被験者について、実験終了時の被験者の肌の状態を、実験例1と同じ評価方法1乃至評価方法3を用いて評価し、その結果を表3に示す。なお、L−アスコルビン酸2−グルコシドの配合量は、L−アスコルビン酸に換算した量を表3に示した。なお、実験例3と、実験例1、実験例2とは、何れも被験者が重複しないように実験を行った。
<Experimental example 3: Effect of blending ratio of hyaluronic acid and L-ascorbic acid in composition for oral consumption on skin>
Since it was confirmed in Experimental Example 1 that hyaluronic acid and L-ascorbic acid were orally ingested to improve skin looseness, wrinkles and wrinkles, hyaluronic acid in the composition for oral ingestion and The test which investigates the influence which the mixing | blending ratio with L-ascorbic acid has on the skin was done as follows. That is, hyaluronic acid, L-ascorbic acid 2-glucoside (Hayashibara Shoji Co., Ltd., trade name “Asco Fresh”), sucrose fatty acid ester, and refined maltose as excipient (Hayashibara Shoji Co., Ltd., trade name “Sanmaruto” S ") was mixed at a mass ratio shown in Table 3 to make the total amount 10 parts by weight, and this was tableted by a conventional method to prepare 0.3 g / tablet tablets each. For each formulation, 17 subjects each were orally ingested 6 tablets per day for 3 months. For each subject, the skin condition of the subject at the end of the experiment was evaluated using the same evaluation method 1 to evaluation method 3 as in Experimental Example 1, and the results are shown in Table 3. In addition, the compounding quantity of L-ascorbic acid 2-glucoside showed the quantity converted into L-ascorbic acid in Table 3. Note that in Experiment Example 3, Experiment Example 1, and Experiment Example 2, the experiment was performed so that the subjects did not overlap.

Figure 2007063177
Figure 2007063177

表3から明らかなように、ヒアルロン酸とL−アスコルビン酸を、質量比で1:4乃至4:1(配合No.3乃至配合No.9)の割合で、とりわけ1:2乃至2:1の割合で配合した錠剤を摂取した場合(配合No.5乃至配合No.7)には、評価に使用した角質の水分蒸散量、角層の重層剥離の程度、肌のかさつきの程度、肌の弛み、シワ及びコジワの改善の何れの項目においても、改善が認められた。これに対して、ヒアルロン酸とL−アスコルビン酸を、0.1:1.9(配合No.1)、0.2:1.8(配合No.2)、1.8:0.2(配合No.10)、或いは、1.9:0.1(配合No.11)の配合割合としたものでは、肌の弛み、シワ及びコジワについては、何れも摂取前に比して改善は認められなかった。   As is apparent from Table 3, hyaluronic acid and L-ascorbic acid were mixed at a mass ratio of 1: 4 to 4: 1 (formulation No. 3 to formulation No. 9), particularly 1: 2 to 2: 1. Ingestion of tablets formulated at a ratio of (No. 5 to No. 7), the amount of transpiration of keratin used in the evaluation, the degree of exfoliation of the stratum corneum, the degree of skin roughness, Improvement was recognized in any of the items of improvement of sagging, wrinkles and wrinkles. On the other hand, hyaluronic acid and L-ascorbic acid were 0.1: 1.9 (formulation No. 1), 0.2: 1.8 (formulation No. 2), 1.8: 0.2 ( In the blending ratio of No. 10) or 1.9: 0.1 (blending No. 11), the skin looseness, wrinkles and wrinkles were all improved compared to before intake. I couldn't.

これらの実験結果は、ヒアルロン酸とL−アスコルビン酸に換算したときのL−アスコルビン酸類とを、質量比で1:4乃至4:1の割合で、さらに望ましくは1:2乃至2:1の割合で配合した経口摂取用組成物が、肌の弛み、シワ及びコジワを改善し、潤いのある肌とする、優れた美肌作用を有していることを物語っている。   These experimental results show that hyaluronic acid and L-ascorbic acid converted to L-ascorbic acid are in a mass ratio of 1: 4 to 4: 1, more preferably 1: 2 to 2: 1. It indicates that the composition for oral intake formulated in a proportion has excellent skin-beautifying action that improves skin slackness, wrinkles and wrinkles, and makes the skin moist.

以下、実施例により本発明をさらに詳細に説明するが、本発明はこれら実施例に何ら限定されるものではない。   EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited to these Examples at all.

<美肌用の経口摂取用組成物>
精製マルトース(株式会社林原商事販売、
商品名「サンマルトS」) 63.5質量部
含水結晶α,α−トレハロース(株式会社
林原商事販売、商品名「トレハ」) 25質量部
滑沢剤 5質量部
牡蠣殻カルシウム 2質量部
ヒアルロン酸 2質量部
L−アスコルビン酸2−グルコシド(株式会社
林原商事販売、商品名「アスコフレッシユ」) 1質量部
糖転移ルチン(東洋精糖株式会社販売、商品名
「αGルチンP」) 0.5質量部
酸味料(有機酸類) 適 量
レモン及びライムのフレーバー 適 量
全量を100質量部とし、これらの成分を均質になるまで攪拌混合し、常法により、0.5gずつ打錠して、錠剤を調製した。
<Composition for oral intake for beautiful skin>
Refined maltose (Hayashibara Corporation sales,
Product name “Sanmalto S”) 63.5 parts by weight Water-containing crystal α, α-trehalose (Hayashibara Shoji Co., Ltd., trade name “Treha”) 25 parts by weight Lubricant 5 parts by weight Oyster shell calcium 2 parts by weight Hyaluronic acid 2 1 part by mass L-ascorbic acid 2-glucoside (trade name “Asco-Freshille” sold by Hayashibara Shoji Co., Ltd.) 1 part by mass sugar transfer rutin (sold by Toyo Seika Co., Ltd., trade name “αG rutin P”) 0.5 part by mass Acidulant (organic acids) Appropriate amount Lemon and lime flavor Appropriate amount Make the total amount 100 parts by weight, stir and mix these ingredients until homogenous, and tablet by 0.5g by a conventional method to prepare tablets did.

本品は、肌の弛み、シワ及び/又はコジワを改善することができる。また、本品は、角層のバリア機能を改善し、皮膚の保水力を高め、肌荒れの改善し、肌のうるおいの向上することができる。本品はこれらの作用効果を標榜して、美肌用の健康補助食品として販売することもできる。   This product can improve skin looseness, wrinkles and / or wrinkles. In addition, this product can improve the barrier function of the stratum corneum, increase the water retention capacity of the skin, improve the rough skin, and improve the moisture of the skin. This product can also be marketed as a health supplement for beautifying skin with these action effects.

<美肌用の経口摂取用組成物>
粉末マルチトール 500質量部
アスコルビン酸2−グルコシド(株式会社
林原商事販売、商品名「アスコフレッシユ」) 50質量部
ヒアルロン酸 25質量部
粉末卵黄 190質量部
脱脂粉乳 200質量部
塩化ナトリウム 4.4質量部
塩化カリウム 1.85質量部
硫酸マグネシウム 4質量部
コンドロイチン硫酸 0.1質量部
グルコサミン 0.5質量部
チアミン 0.01質量部
ビタミンEアセテート 0.6質量部
ニコチン酸アミド 0.04質量部
コエンザイムQ10 0.03質量部
糖転移ヘスペリジン(東洋精糖株式会社販売、
商品名「αGヘスペリジンPS」) 0.02質量部
上記配合組成からなる配合物を調製した。この配合物25質量部を精製水150質量部に均一に分散・溶解させ、200gずつ褐色ガラス瓶に封入した。
<Composition for oral intake for beautiful skin>
Powdered maltitol 500 parts by weight Ascorbic acid 2-glucoside (Hayashibara Shoji Co., Ltd., trade name “ASCO Fresh”) 50 parts by weight Hyaluronic acid 25 parts by weight Powdered egg yolk 190 parts by weight Nonfat dry milk 200 parts by weight Sodium chloride 4.4 parts by weight Part Potassium chloride 1.85 parts by weight Magnesium sulfate 4 parts by weight Chondroitin sulfate 0.1 part by weight Glucosamine 0.5 part by weight Thiamine 0.01 part by weight Vitamin E acetate 0.6 part by weight Nicotinamide 0.04 part by weight Coenzyme Q10 0.03 parts by mass glycosylated hesperidin (sold by Toyo Seika Co., Ltd.,
(Product name “αG Hesperidin PS”) 0.02 parts by mass A composition comprising the above composition was prepared. 25 parts by mass of this formulation was uniformly dispersed and dissolved in 150 parts by mass of purified water, and 200 g each was enclosed in a brown glass bottle.

本品は、肌の弛み、シワ及び/又はコジワを改善することができる。また、本品は、角層のバリア機能を改善し、皮膚の保水力を高め、肌荒れの改善し、肌のうるおいの向上することができる。本品はこれらの作用効果を標榜して、美肌用の健康補助食品として販売することもできる。なお、本品は、ヒトのみならず、家畜、ペットなどの動物のための経口摂取又は、胃や腸へゾンデ等を使用して直接投与する経管投与用の組成物としても有利に利用できる。また、本品は糖転移ヘスペリジンを含んでいるので、血中脂質や血中コレステロールなどの、血中脂質の低減のために用いられる旨を標榜することも随意である。   This product can improve skin looseness, wrinkles and / or wrinkles. In addition, this product can improve the barrier function of the stratum corneum, increase the water retention capacity of the skin, improve the rough skin, and improve the moisture of the skin. This product can also be marketed as a health supplement for beautifying skin with these action effects. In addition, this product can be advantageously used as a composition for oral ingestion not only for humans but also for animals such as domestic animals and pets, or for direct administration using a sonde or the like to the stomach or intestine. . In addition, since this product contains transglycosylated hesperidin, it is also optional to advocate that it is used to reduce blood lipids such as blood lipids and blood cholesterol.

<美肌用の経口摂取用組成物>
粉末マルチトール 25質量部
含水結晶α,α−トレハロース(株式会社林原商事
販売、商品名「トレハ」) 54質量部
滑沢剤 3質量部
L−アスコルビン酸2−グルコシド(株式会社
林原商事販売、商品名「アスコフレッシユ」) 10質量部
グルコサミン 2.5質量部
コンドロイチン硫酸ナトリウム 1.5質量部
ヒアルロン酸 4質量部
上記配合処方に基づき、これらの成分を均質になるまで攪拌混合し、常法により、0.5gずつ打錠して、錠剤を調製した。
<Composition for oral intake for beautiful skin>
Powdered maltitol 25 parts by weight Hydrous crystals α, α-trehalose (Hayashibara Corporation, trade name “Treha”) 54 parts by weight Lubricant 3 parts by weight L-ascorbic acid 2-glucoside (Hayashibara Corporation sales, product) 10 parts by weight Glucosamine 2.5 parts by weight Sodium chondroitin sulfate 1.5 parts by weight Hyaluronic acid 4 parts by weight Based on the above formulation, these ingredients are stirred and mixed until homogenous, Tablets were prepared by tableting 0.5 g each.

本品は、肌の弛み、シワ及び/又はコジワを改善することができる。また、本品は、角層のバリア機能を改善し、皮膚の保水力を高め、肌荒れの改善し、肌のうるおいの向上することができる。本品はこれらの作用効果を標榜して、美肌用の健康補助食品として販売することもできる。   This product can improve skin looseness, wrinkles and / or wrinkles. In addition, this product can improve the barrier function of the stratum corneum, increase the water retention capacity of the skin, improve the rough skin, and improve the moisture of the skin. This product can also be marketed as a health supplement for beautifying skin with these action effects.

本発明の経口摂取用組成物を摂取することにより、肌の弛み、シワ及び/又はコジワを改善することができるだけでなく、肌のバリア機能を高め、肌の保水力を高めることができるので、肌を美しく保つことができる。本発明は、斯くも顕著な作用効果を奏する発明であり、斯界に多大の貢献をする、誠に意義のある発明である。   By ingesting the composition for oral consumption of the present invention, not only can it improve skin slackness, wrinkles and / or wrinkles, but also can enhance the skin barrier function and increase the water retention capacity of the skin, Can keep skin beautiful. The present invention is an invention that exhibits such remarkable effects, and is a truly significant invention that contributes greatly to the world.

Claims (5)

ヒアルロン酸とL−アスコルビン酸に換算したときのL−アスコルビン酸類との配合割合が、質量比で1:4乃至4:1であることを特徴とする美肌用の経口摂取用組成物。   An orally ingestible composition for beautiful skin, wherein the blending ratio of hyaluronic acid and L-ascorbic acid when converted to L-ascorbic acid is 1: 4 to 4: 1 by mass ratio. さらに、コンドロイチン硫酸及び/又はグルコサミンを含有することを特徴とする請求項1記載の美肌用の経口摂取用組成物。   Furthermore, chondroitin sulfate and / or glucosamine is contained, The composition for oral intake for the beautiful skin of Claim 1 characterized by the above-mentioned. L−アスコルビン酸類が、L−アスコルビン酸2−グルコシドであることを特徴とする請求項1又は2記載の美肌用の経口摂取用組成物。   L-ascorbic acid is L-ascorbic acid 2-glucoside, The composition for oral intake of the beautiful skin of Claim 1 or 2 characterized by the above-mentioned. 美肌作用を有することを標榜してなる請求項1乃至3の何れかに記載の美肌用の経口摂取用組成物。   4. The composition for oral intake for beautifying skin according to any one of claims 1 to 3, wherein it is advocated to have a beautifying skin action. 肌の弛み、シワ及び/又はコジワの改善剤・抑制剤としての請求項1乃至4の何れかに記載の美肌用の経口摂取用組成物。   The composition for oral ingestion for beautiful skin according to any one of claims 1 to 4, as an improver / inhibitor for skin looseness, wrinkles and / or wrinkles.
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US20110171286A1 (en) * 2010-01-13 2011-07-14 Allergan, Inc. Hyaluronic acid compositions for dermatological use
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US8318695B2 (en) 2007-07-30 2012-11-27 Allergan, Inc. Tunably crosslinked polysaccharide compositions
US8338375B2 (en) 2007-05-23 2012-12-25 Allergan, Inc. Packaged product
US8338388B2 (en) 2003-04-10 2012-12-25 Allergan, Inc. Cross-linking of low-molecular weight and high-molecular weight polysaccharides, preparation of injectable monophase hydrogels, polysaccharides and hydrogels obtained
JPWO2011007885A1 (en) * 2009-07-16 2012-12-27 サンスター株式会社 Contains proteoglycan
US8357795B2 (en) 2008-08-04 2013-01-22 Allergan, Inc. Hyaluronic acid-based gels including lidocaine
US8394782B2 (en) 2007-11-30 2013-03-12 Allergan, Inc. Polysaccharide gel formulation having increased longevity
US8394784B2 (en) 2007-11-30 2013-03-12 Allergan, Inc. Polysaccharide gel formulation having multi-stage bioactive agent delivery
US8586562B2 (en) 2010-03-12 2013-11-19 Allergan Industrie, Sas Fluid compositions for improving skin conditions
US8691279B2 (en) 2010-03-22 2014-04-08 Allergan, Inc. Polysaccharide and protein-polysaccharide cross-linked hydrogels for soft tissue augmentation
US8697044B2 (en) 2007-10-09 2014-04-15 Allergan, Inc. Crossed-linked hyaluronic acid and collagen and uses thereof
US8697057B2 (en) 2010-08-19 2014-04-15 Allergan, Inc. Compositions and soft tissue replacement methods
US8883139B2 (en) 2010-08-19 2014-11-11 Allergan Inc. Compositions and soft tissue replacement methods
US8889123B2 (en) 2010-08-19 2014-11-18 Allergan, Inc. Compositions and soft tissue replacement methods
US8946192B2 (en) 2010-01-13 2015-02-03 Allergan, Inc. Heat stable hyaluronic acid compositions for dermatological use
US9005605B2 (en) 2010-08-19 2015-04-14 Allergan, Inc. Compositions and soft tissue replacement methods
US9114188B2 (en) 2010-01-13 2015-08-25 Allergan, Industrie, S.A.S. Stable hydrogel compositions including additives
US9149422B2 (en) 2011-06-03 2015-10-06 Allergan, Inc. Dermal filler compositions including antioxidants
US9228027B2 (en) 2008-09-02 2016-01-05 Allergan Holdings France S.A.S. Threads of Hyaluronic acid and/or derivatives thereof, methods of making thereof and uses thereof
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US9284359B2 (en) 2011-01-19 2016-03-15 Hirosaki University Method for mass preparation of proteoglycan
JP2016069286A (en) * 2014-09-26 2016-05-09 株式会社ファンケル L-ascorbic acid sustained-release formulation
US9393263B2 (en) 2011-06-03 2016-07-19 Allergan, Inc. Dermal filler compositions including antioxidants
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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0967262A (en) * 1995-08-31 1997-03-11 Shiseido Co Ltd Skin activator and skin activating food
JP2002223726A (en) * 2001-01-31 2002-08-13 Ribateepu Seiyaku Kk Food for beauty
JP2003095961A (en) * 2001-09-27 2003-04-03 Combi Corp Skin beautifying promoter
JP2004250372A (en) * 2003-02-20 2004-09-09 Fancl Corp Skin aging inhibitor/improver and/or rough skin inhibitor/improver kit
JP2006265287A (en) * 2005-03-22 2006-10-05 Q P Corp Low molecular weight hyaluronic acid and/or its salt, its manufacturing process and cosmetic and food composition containing it
JP2007043960A (en) * 2005-08-10 2007-02-22 Towa Kagaku Kk Energy-promoting/aging-preventing jellied food and method for producing the same

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0967262A (en) * 1995-08-31 1997-03-11 Shiseido Co Ltd Skin activator and skin activating food
JP2002223726A (en) * 2001-01-31 2002-08-13 Ribateepu Seiyaku Kk Food for beauty
JP2003095961A (en) * 2001-09-27 2003-04-03 Combi Corp Skin beautifying promoter
JP2004250372A (en) * 2003-02-20 2004-09-09 Fancl Corp Skin aging inhibitor/improver and/or rough skin inhibitor/improver kit
JP2006265287A (en) * 2005-03-22 2006-10-05 Q P Corp Low molecular weight hyaluronic acid and/or its salt, its manufacturing process and cosmetic and food composition containing it
JP2007043960A (en) * 2005-08-10 2007-02-22 Towa Kagaku Kk Energy-promoting/aging-preventing jellied food and method for producing the same

Cited By (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11045490B2 (en) 2003-04-10 2021-06-29 Allergan Industrie, Sas Injectable monophase hydrogels
US10653716B2 (en) 2003-04-10 2020-05-19 Allergan Industrie, Sas Injectable monophase hydrogels
US10080767B2 (en) 2003-04-10 2018-09-25 Allergan Industrie Sas Injectable monophase hydrogels
US8563532B2 (en) 2003-04-10 2013-10-22 Allergan Industrie Sas Cross-linking of low-molecular weight and high-molecular weight polysaccharides, preparation of injectable monophase hydrogels, polysaccharides and hydrogels obtained
US8338388B2 (en) 2003-04-10 2012-12-25 Allergan, Inc. Cross-linking of low-molecular weight and high-molecular weight polysaccharides, preparation of injectable monophase hydrogels, polysaccharides and hydrogels obtained
US9062130B2 (en) 2003-04-10 2015-06-23 Allergan Industrie Sas Cross-linking of low-molecular weight and high-molecular weight polysaccharides, preparation of injectable monophase hydrogels, polysaccharides and hydrogels obtained
US8338375B2 (en) 2007-05-23 2012-12-25 Allergan, Inc. Packaged product
US8318695B2 (en) 2007-07-30 2012-11-27 Allergan, Inc. Tunably crosslinked polysaccharide compositions
US8703118B2 (en) 2007-10-09 2014-04-22 Allergan, Inc. Crossed-linked hyaluronic acid and collagen and uses thereof
US8697044B2 (en) 2007-10-09 2014-04-15 Allergan, Inc. Crossed-linked hyaluronic acid and collagen and uses thereof
US9265761B2 (en) 2007-11-16 2016-02-23 Allergan, Inc. Compositions and methods for treating purpura
US8394782B2 (en) 2007-11-30 2013-03-12 Allergan, Inc. Polysaccharide gel formulation having increased longevity
US8394784B2 (en) 2007-11-30 2013-03-12 Allergan, Inc. Polysaccharide gel formulation having multi-stage bioactive agent delivery
US8394783B2 (en) 2007-11-30 2013-03-12 Allergan, Inc. Polysaccharide gel formulation having multi-stage bioactive agent delivery
US8853184B2 (en) 2007-11-30 2014-10-07 Allergan, Inc. Polysaccharide gel formulation having increased longevity
US8513216B2 (en) 2007-11-30 2013-08-20 Allergan, Inc. Polysaccharide gel formulation having increased longevity
US8357782B2 (en) 2008-03-21 2013-01-22 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo Monoclonal antibodies specific for human interferon-alpha subtype alpha 8
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US9238013B2 (en) 2008-08-04 2016-01-19 Allergan Industrie, Sas Hyaluronic acid-based gels including lidocaine
US9089517B2 (en) 2008-08-04 2015-07-28 Allergan Industrie Sas Hyaluronic acid-based gels including lidocaine
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US9089518B2 (en) 2008-08-04 2015-07-28 Allergan Industrie Sas Hyaluronic acid-based gels including lidocaine
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US9861570B2 (en) 2008-09-02 2018-01-09 Allergan Holdings France S.A.S. Threads of hyaluronic acid and/or derivatives thereof, methods of making thereof and uses thereof
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JP5933264B2 (en) * 2009-07-16 2016-06-08 サンスター株式会社 Contains proteoglycan
JPWO2011007885A1 (en) * 2009-07-16 2012-12-27 サンスター株式会社 Contains proteoglycan
US9585828B2 (en) 2009-07-16 2017-03-07 Sunstar Inc. Proteoglycan-containing material
US9265781B2 (en) 2009-09-03 2016-02-23 Hayashibara Co., Ltd. Process for producing a particulate composition comprising anhydrous crystalline 2-O-alpha-D-glucosyl-L-ascorbic acid
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US8765416B2 (en) 2009-09-03 2014-07-01 Hayashibara Co., Ltd. Particulate composition containing anhydrous crystalline 2-O-alpha-D-glucosyl-L-ascorbic acid, process for producing the same, and uses thereof
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US20120225842A1 (en) * 2010-01-13 2012-09-06 Allergan, Inc. Hyaluronic acid compositions for dermatological use
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