JP7457650B2 - テオブロマカカオl豆の加水分解物、少なくとも一つのプレバイオティクスおよびプロバイオティクスの含むメイクアップ組成物 - Google Patents
テオブロマカカオl豆の加水分解物、少なくとも一つのプレバイオティクスおよびプロバイオティクスの含むメイクアップ組成物 Download PDFInfo
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- Cosmetics (AREA)
Description
-一過性菌叢:一過性菌叢は、環境から腐敗した有機物を餌とする腐生菌と称される、大抵は無害な真菌、ウイルスおよび細菌からなる。この菌叢は恒久的なものではなく、行われる活動や周辺条件の変化、個体がこれらの条件に露出されることに応じて日中に変化する。最も一般的な一過性菌叢の種としては、スタフィルオコックス・アウロイス(Staphylococcus aureus)、エスケリキア・コリ(Escherichia coli)、シュードモナス・アエルギノーサ(Pseudomonas aeruginosa)およびバチルス(Bacillus)の種がある。
-常在菌叢:常在菌叢は共生菌からなり、すなわちそれらの宿主のおかげで何の損傷も与えずに生きている。この菌叢の構成は固定されており、妨害された後、同じ構成に自発的に再形成される。これらの微生物(グラム陽性細菌、グラム陰性細菌など)は表皮に生息しており、主に角質層の上層ならびに汗腺や毛嚢脂腺の毛包(pilosebaceous follicle)の管、爪や毛髪のような表皮付属器で見つかられる。
-細胞凝集の構成要素を形成し、それによって表皮の抵抗力を形成するタンパク質であるデスモグレイン-1の形成を減少させることにより(Straseski J et al. Wound Repair Regen. 2009; 17(4): 606-616)
-また水分を表皮に輸送し、皮膚に水分補給するタンパク質であるアクアポリン3の形成を減少させることにより(Straseski J et al. Wound Repair Regen. 2009; 17(4): 606-616)
-皮膚の構成成分や細胞を変化させる活性酸素種(ROS)の産生を刺激することにより(Nys K et al. Free Radic Biol Med. 2012;52(6):1111-20)
-ケラチン10などの分化ケラチンの形成を抑制することにより(Straseski J et al. Wound Repair Regen. 2009; 17(4): 606-616)、および/または
-マトリックスメタロプロテアーゼまたはMMPの存在を増加させることにより(Xia YP et al. J. Invest. Dermatol. 2001; 116: 50-56)、コラーゲンなどの皮膚の構成成分を壊し、皮膚密集度や弾力に影響を与え、その結果として、毛穴の開きおよび細かい線やしわの形成をもたらし得る。
-皮膚バリアの強化や皮脂産生の制御などが可能な皮膚状態を提供することで、微生物叢およびその多様性を維持することにより、
-表皮の凝集を高め、皮膚の抵抗力を強化することにより、
-皮膚バリアの形成を刺激し、皮膚に十分な水分を維持することにより、
-皮膚の活性酸素種を無毒化することにより、
-MMPの形成を抑制することにより、および/または
-低酸素症から皮膚細胞を保護する低酸素症誘導因子またはHIFの形成を刺激することにより。
a)テオブロマカカオL豆の加水分解物、
b)プレバイオティクスおよびプロバイオティクス、ならびに
c)一つまたはそれ以上の色材。
本発明によれば、「ケラチン物質」とは、皮膚、粘膜(特に唇)および毛髪および爪を意味する。特定の実施態様によれば、組成物は、皮膚、唇または毛髪および爪、好ましくは皮膚への局所適用を目的とする。
したがって、本発明の第一の目的は、ケラチン物質、特に皮膚、唇または眼、好ましくは皮膚をメイクアップするための化粧品組成物であって、生理学的に許容できる媒体中に、少なくとも以下の物質を含む化粧品組成物に関する:
a)テオブロマカカオL豆の加水分解物;
b)プレバイオティクスおよびプロバイオティクス;ならびに
c)一つまたはそれ以上の色材。
本発明によるテオブロマカカオL豆の加水分解物は、主にペプチドおよびサッカライドを含む、テオブロマカカオL豆のペプチドおよびサッカライド加水分解物である。用語「主にペプチドおよびサッカライド」とは、50%を超える量、好ましくは60%を超える量、好ましくは70%を超える量、最大90%(重量/重量)のペプチドおよびサッカライドの乾燥物質、好ましくは90%の乾燥物質を意味する。
a)挽いたテオブロマカカオL豆を水相中に分散させ;
b)工程a)で得られる水分散液を酵素処理し;
c)固液分離により酵素加水分解物を回収し;
d)超ナノ濾過により加水分解物精製し、その後、場合により
e)工程d)で得られる加水分解物を凍結乾燥させる。
「プレバイオティクス」とは、ヒトの健康に有益な腸のプロバイオティクス菌株(ラクトバシリ(lactobacilli)、ビフィズス菌など)およびほかの細菌の菌株の増殖や活性を調節する性質を有する非生物性食品成分を意味する。プレバイオティクスは、一般に果物や植物、蜂蜜などに自然に存在する抽出可能な単糖類、二糖類またはオリゴ糖類である。他は、多糖(例えばオリゴフルクトースまたはフルクト-オリゴ糖、略称FOS)の加水分解により工業的に生産するか、またはラクトースなどの二糖類に転移活性を有するラクターゼなどの酵素の作用を受けさせ、トランス-ガラクト-オリゴ糖(TOS)を生成するか、もしくは化学異性化反応によりラクツロースを生成することによって合成する。現在、プレバイオティクス効果が認められているものとしては、トランス-ガラクトオリゴ糖(GOS)やイヌリン型フルクタン類が挙げられる。
プロバイオティクスは細菌または酵母のどちらか一方であり得る。
本発明の意味での化粧剤は、バイオポリマー、すなわち化学合成によって得られる植物原料物質由来のポリマーからなる。
-モル質量が5~630kDaのガラクトマンナン、および
-モル質量が7~3000kDaの架橋硫酸化ガラクタンからなる。
-平均モル質量が5~120kDaのガラクトマンナンおよび平均モル質量が7~1100kDaの架橋硫酸化ガラクタンからなる。
-平均モル質量が8~80kDaのガラクトマンナンおよび平均モル質量が8~200kDaの架橋硫酸化ガラクタンからなる。
-天然ガラクトマンナン粉末または天然硫酸化ガラクタンそれぞれの水への溶解化
-化学的または酵素的ルートによる加水分解
-不溶性相を除去するための、可溶性相または不溶性相の分離
-規定のモル質量のガラクトマンナンの膜濾過による選択
本明細書による組成物は、少なくとも一つの、水溶性または非水溶性色材、脂溶性または無脂肪色材、有機または無機色材、光学効果原料物質およびこれらの混合物から選択されてもよい色材を含む。
本発明による組成物は、より詳しくは、ケラチン物質、特に皮膚への局所適用を目的とする。本発明の組成物は、化粧品分野、特にケラチン物質への局所適用を目的とする組成物であり、それらをメイクアップする目的で皮膚への局所適用を目的としてない、または適していない食品組成物とは区別される。
-皮膚の微生物叢の生物多様性および恒常性(活性成分であるActibiome(C)(水および海水およびグリセリンおよびラミナリア・ディギタータ(Laminaria digitata)抽出物およびクロレラ・ブルガリス(Chlorella vulgaris)抽出物および異性化糖(saccharide isomerate)およびフェノキシエタノールおよびエチルヘキシルグリセリン)のように、ストレスの期間によってあらかじめ低下された皮膚のpHを再調整することにより);
-細胞再生(酸性のpHで「ピーリング」効果がある活性成分の単独または組み合わせにより):
・化学的手段(αヒドロキシ酸(AHA)(グリコール酸、乳酸、クエン酸...)、βヒドロキシ酸(BHA)(サリチル酸)、ポリヒドロキシ酸(PHA)(グルコノラクトン)など)により;
・生物学的手段(Exfolactive C EL PX(C)(オプンティア・コチネリフェラ(Opuntia coccinellifera))、DERMOCH DP(C)(Chlorella vulgaris)、ALGOWHITE(C)(アスコフィラム・ノドサム(Ascophyllum nodosum)など)により
・酵素経路(MELACLEAR(C)(グルコン酸、スティラインズ))により;
-顔の肌の再生または再活性化(輝き)(以下の活性成分を用いて):
・レチノールのような平滑化(ビタミンA様)
・メラニン生成に作用することによるライトナー(ビタミンC誘導体)
・エネルギー付与剤(energizer)(栄養素および/または抗酸化剤であるビタミンCおよびビタミンE(SEPIVITAL(C)(リン酸アスコルビルトコフェロールカリウム)など)など);
-皮脂産生の減少(セボトラッピング剤(sebo-trapping agent)(クレイ)または、グルコン酸亜鉛(Mineralis GU/Zn)およびアボカドリポフィル抽出物(5αavocuta)などの皮脂調節活性剤(sebo-regulating active agent)を用いて);
-外部からの侵入(汚染、ブルーライト、化学的または鉱物フィルターを使用および/または反射粒子を拡散させるUV、またはこれらの混合物)からの保護。
これらの活性成分を単独または組み合わせて用いた転写効果に関する研究は、TaqMan Low Density Array(TLDA)技術を用いて行った。この技術のおかげで、正常なヒト角化細胞(ケラチン生成細胞)の処置に応じた、特定のタンパク質をコードする遺伝子の発現の変調が研究され、これは、上記活性成分の単独または組み合わせでの遺伝子発現のマッピングを可能にした。
用いられた細胞:正常ヒト表皮角化細胞
培地: HKGS(ヒト-角化細胞-増殖-サプリメント)が補充されたEpiLife(R)
細胞の皮膚由来:腹部採取、女性、47歳
研究モデル:TaqMan Low Density Array (TLDA)技術
化合物での細胞の処理:24時間
・0.25%のECOSKIN(R)(α-グルカンオリゴ糖およびヤーコン(Polymnia Sonchifolia)根の搾汁およびマルトデキストリンおよびラクトバシラス(Lactobacillus))
・0.05%のBLUMILIGHTTM(ブチレングリコールおよび水およびテオブロマカカオ(ココア) 種子抽出物)
・0.25%のECOSKIN(R)+0.05%のBLUMILIGHTTMの組み合わせ
以下の表1は、研究した遺伝子の活性の変動を示している。
-各試験は、3回実施する(未処理の3回、同一条件で処理される3回);
-Fischer F-検定は、最初に2つのデータ行列を比較することによって適用する。値がα= 0.05より大きい場合、スチューデントのt-検定の分散は2で、FischerのF-検定がα= 0.05より小さい場合、分散は3になる。
-保持される転写変動(有意)は、スチューデントのt検定においてα(またはp)=0.05未満またはそれに等しく対応するものになる。抑制は淡い灰色で示し、刺激は濃い灰色(下記参照)で示し、白色の背景は、有意でない変動、すなわちスチューデントのt検定においてα(またはp)=0.05より大きく対応するものを示す。
-「測定されていない」の表示「ND」は、遺伝子の転写活性が小さすぎて、使用されるTLDA方法により定量化することができないことを意味する。
-皮膚表皮の適当な発達および、その表面の均質性および質を確保するその落屑を促進させ、特に、KRT1、KLK7およびZNF750などの遺伝子の活性を刺激することにより、落屑および/または表皮再生を促進させる。
-TGM1、PLIN1、DSG1、SPRR1B、PI3遺伝子の活性を刺激することにより、皮膚バリアを改善および/または強化し、こうして、内部および外部因子からの皮膚保護を促進させる。
-ABCC2、GPX4、GSR、PRDX3、SEPW1遺伝子の活性を刺激することにより、ストレスを無毒化することによって、ストレス(例えば酸化的ストレス)に対する皮膚の抵抗力を改善および/または強化する。
-MMP3、MMP9、MMP10およびCTSS遺伝子の活性を抑制することにより、毛穴の開きを制限し、皮膚を緻密化する弾力(firmness)の損失を低下させ、細かい線やしわの形成を減少させる。
-IL8およびCSF2の炎症遺伝子を抑制し、PIAS3阻害遺伝子を活性化することにより、皮膚を鎮静させ、それによって皮膚の快適さおよび平坦度を改善する。
-PI3およびKL7遺伝子を刺激することにより、微生物叢の発達を調節し、皮膚の恒常性を確保し、特に、皮膚生態系を維持し、および/または皮膚の微生物叢、特に微生物多様性を維持する。
脂性肌は、皮脂腺の分泌産物である皮脂がその表面に過度に存在することを特徴とする。この皮脂の産生は、より詳しくは、脂質生成と呼ばれる脂質の細胞分化および合成または蓄積の過程を通して、脂腺細胞によって確保される。脂質生成は、インビトロで実験的に理解できる多くの因子(食事、活性成分など)の影響を受ける。
用いられた細胞:適切な培地中の皮脂腺細胞(培養条件:37℃、5% CO2)
試験培地:25μg/mlのゲンタマイシンが補充されたKeratinocytes-SFM(無血清培地)(商品名)
研究試料:脂肪合成因子(ビタミンD3 50nM+ビタミンC 50μg/ml+インスリン 5μg/ml+カルシウム 1.5mM)により刺激されたヒト脂腺細胞株
対照群:未処理で未刺激のヒト脂腺細胞株+未処理で脂肪合成因子により刺激されたヒト脂腺細胞株
方法:RT-qPCR
試験化合物:
・0.25%のECOSKIN(R)(α-グルカンオリゴ糖およびヤーコン(Polymnia Sonchifolia)根の搾汁およびマルトデキストリンおよびラクトバシラス(Lactobacillus))
・0.05%のBLUMILIGHTTM(ブチレングリコールおよび水およびテオブロマカカオ(ココア)種子抽出物)
-皮脂依存性炎症遺伝子であるIL1βおよびTNFの抑制し、皮脂を制御し、ファンデーションの皮膚表面への持ちおよび付着を改善し、
-細胞外マトリックス(コラーゲン、プロテオグリカン、ラミニン、など)の分解遺伝子(MMP9、MMP1、MMP2、MMP3およびCTSK)を抑制することにより、より良い皮膚のきめやファンデーションの皮膚へのより良い均質性を確保する毛穴弛緩を制限する
Claims (18)
- ケラチン物質をメイクアップするための化粧品組成物であって、生理学的に許容できる媒体中に、少なくとも以下の物質を含む化粧品組成物:
a)テオブロマカカオL豆の加水分解物、
b)α-グルコ-オリゴ糖、ヤーコン根抽出物、ラクトバチルス属細菌溶解物およびマルトデキストリンを含むプレ/プロバイオティクス複合体の形態である、プレバイオティクスおよびプロバイオティクス、ならびに
c)一つまたはそれ以上の色材。 - 化粧品組成物が、皮膚、唇または眼のためのものであることを特徴とする、請求項1に記載の化粧品組成物。
- 化粧品組成物が、皮膚をメイクアップするためのものであることを特徴とする、請求項1に記載の化粧品組成物。
- テオブロマカカオL豆の加水分解物が、テオブロマカカオL豆のペプチドおよびサッカライド加水分解物であることを特徴とする、請求項1~3のいずれか一項に記載の化粧品組成物。
- ペプチドおよびサッカライドが、200Da~10kDaの分子量を有することを特徴とする、請求項4に記載の化粧品組成物。
- テオブロマカカオL豆の加水分解物が、組成物総重量に対して0.0005重量%~0.025重量%の範囲の活性成分の含有量で組成物中に存在することを特徴とする、請求項1~5のいずれか一項に記載の化粧品組成物。
- テオブロマカカオL豆の加水分解物が、組成物総重量に対して0.001重量%~0.01重量%の範囲の活性成分の含有量で組成物中に存在することを特徴とする、請求項6に記載の化粧品組成物。
- プレバイオティクスおよびプロバイオティクスが、組成物総重量に対して0.05重量%~3重量%の範囲の活性成分の総含有量で組成物中に存在することを特徴とする、請求項1~7のいずれか一項に記載の化粧品組成物。
- プレバイオティクスおよびプロバイオティクスが、組成物総重量に対して0.1重量%~1重量%の範囲の活性成分の総含有量で組成物中に存在することを特徴とする、請求項8に記載の化粧品組成物。
- 一つまたはそれ以上の色材が、鉱物および/または有機顔料、複合顔料、着色剤、真珠層または真珠光沢顔料、およびこれらの混合物から選択されることを特徴とする、請求項1~9のいずれか一項に記載の化粧品組成物。
- 一つまたはそれ以上の色材が、組成物総重量に対して2重量%~30重量%の範囲の含有量で組成物中に存在することを特徴とする、請求項1~10のいずれか一項に記載の化粧品組成物。
- 一つまたはそれ以上の色材が、組成物総重量に対して4重量%~15重量%の範囲の含有量で組成物中に存在することを特徴とする、請求項11に記載の化粧品組成物。
- 顔の肌、唇または眼のためのメイクアップ組成物の形態であることを特徴とする、請求項1~12のいずれか一項に記載の化粧品組成物。
- ケラチン物質をメイクアップするための化粧方法であって、請求項1~13のいずれか一項に記載の化粧品組成物を、少なくとも該ケラチン物質に適用することを含む方法。
- 化粧品組成物が、顔の肌のための化粧品組成物であることを特徴とする、請求項14に記載のケラチン物質をメイクアップするための化粧方法。
- さらに皮膚生態系を維持すること、および/または皮膚微生物叢のバランス、微生物多様性を維持すること、皮膚バリアを強化すること、および/またはストレスに対する皮膚の抵抗力を改善すること、を可能にすることを特徴とする、請求項14または15に記載の化粧方法。
- a)テオブロマカカオL豆の加水分解物、
b)α-グルコ-オリゴ糖、ヤーコン根抽出物、ラクトバチルス属細菌溶解物およびマルトデキストリンを含むプレ/プロバイオティクス複合体の形態である、プレバイオティクスおよびプロバイオティクス、
を含む、非治療的化粧品としての使用のための組み合わせ剤であって、該非治療的化粧品としての使用は、皮膚生態系を維持、および/または皮膚微生物叢のバランス、微生物多様性を維持、皮膚バリアを強化、および/またはストレスに対する皮膚の抵抗力を改善するためのものである、組み合わせ剤。 - 非治療的化粧品としての使用のための、請求項1~13のいずれか一項に記載の化粧品組成物であって、該非治療的化粧品としての使用は、皮膚生態系を維持、および/または皮膚微生物叢のバランス、微生物多様性を維持、皮膚バリアを強化、および/またはストレスに対する皮膚の抵抗力を改善するためのものである、化粧品組成物。
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FR1763151 | 2017-12-22 | ||
FR1763151A FR3075647B1 (fr) | 2017-12-22 | 2017-12-22 | Composition de maquillage comprenant un hydrolysat de feves de theobroma cacao l, et au moins un prebiotique et un probiotique |
PCT/FR2018/053508 WO2019122780A1 (fr) | 2017-12-22 | 2018-12-21 | Composition de maquillage comprenant un hydrolysat de fèves de theobroma cacao l, et au moins un prébiotique et un probiotique |
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JP2021508329A JP2021508329A (ja) | 2021-03-04 |
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US (1) | US20210212925A1 (ja) |
EP (1) | EP3727593B1 (ja) |
JP (1) | JP7457650B2 (ja) |
KR (1) | KR20200128516A (ja) |
CN (1) | CN111601583B (ja) |
ES (1) | ES2965918T3 (ja) |
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FR3104421B1 (fr) * | 2019-12-17 | 2022-12-02 | Lvmh Rech | Composition cosmétique comprenant du D-chiro-inositol |
CN113897300B (zh) * | 2021-04-27 | 2023-04-28 | 江南大学 | 一株具有改善皮肤屏障功能损伤与皮肤敏感的动物双歧杆菌 |
FR3148720A1 (fr) | 2023-05-18 | 2024-11-22 | Le Rouge Francais | Composition cosmétique aqueuse contenant un agent probiotique, un composé choisi parmi l'acide hyaluronique et ses dérivés, un colorant particulier et une huile végétale. |
FR3151215A1 (fr) | 2023-07-23 | 2025-01-24 | Le Rouge Francais | Composition cosmétique topique anhydre pulvérulente comprenant un agent probiotique, de l'acide hyaluronique ou un de ses dérivés, un colorant particulier et une poudre minérale particulière. |
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JP2010051250A (ja) * | 2008-08-28 | 2010-03-11 | Ezaki Glico Co Ltd | カカオ発酵処理物およびその製造方法 |
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WO2016142767A1 (en) | 2015-03-09 | 2016-09-15 | Bioimmunizer Sagl | Anti-age composition comprising a combination of antioxidant agents in association with bifidobacteria and cell walls isolated from probiotics |
WO2017157998A1 (fr) | 2016-03-16 | 2017-09-21 | ISP Investments LLC. | Hydrolysat peptidique et osidique des fèves de cacao, compositions cosmetiques le comprenant et leurs utilisations cosmétiques |
WO2017173244A1 (en) | 2016-03-31 | 2017-10-05 | Gojo Industries, Inc. | Topical composition for reducing pathogen binding |
CN107397714A (zh) | 2017-07-19 | 2017-11-28 | 广东丸美生物技术股份有限公司 | 具有抗蓝光污染和淡化细纹功效的精华乳及其制备与应用 |
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KR20200128516A (ko) | 2020-11-13 |
JP2021508329A (ja) | 2021-03-04 |
WO2019122780A9 (fr) | 2019-08-08 |
EP3727593A1 (fr) | 2020-10-28 |
FR3075647B1 (fr) | 2020-05-22 |
US20210212925A1 (en) | 2021-07-15 |
FR3075647A1 (fr) | 2019-06-28 |
WO2019122780A1 (fr) | 2019-06-27 |
CN111601583A (zh) | 2020-08-28 |
EP3727593B1 (fr) | 2023-09-20 |
ES2965918T3 (es) | 2024-04-17 |
CN111601583B (zh) | 2023-08-25 |
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