JP6631805B2 - 白髪化防止のためのヘアケアにおけるエーデルワイス抽出物の使用 - Google Patents
白髪化防止のためのヘアケアにおけるエーデルワイス抽出物の使用 Download PDFInfo
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- JP6631805B2 JP6631805B2 JP2016530144A JP2016530144A JP6631805B2 JP 6631805 B2 JP6631805 B2 JP 6631805B2 JP 2016530144 A JP2016530144 A JP 2016530144A JP 2016530144 A JP2016530144 A JP 2016530144A JP 6631805 B2 JP6631805 B2 JP 6631805B2
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- 229960000943 tartrazine Drugs 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 229940098465 tincture Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 229940042585 tocopherol acetate Drugs 0.000 description 1
- 125000002640 tocopherol group Chemical class 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- QURCVMIEKCOAJU-UHFFFAOYSA-N trans-isoferulic acid Natural products COC1=CC=C(C=CC(O)=O)C=C1O QURCVMIEKCOAJU-UHFFFAOYSA-N 0.000 description 1
- LOIYMIARKYCTBW-OWOJBTEDSA-N trans-urocanic acid Chemical compound OC(=O)\C=C\C1=CNC=N1 LOIYMIARKYCTBW-OWOJBTEDSA-N 0.000 description 1
- LOIYMIARKYCTBW-UHFFFAOYSA-N trans-urocanic acid Natural products OC(=O)C=CC1=CNC=N1 LOIYMIARKYCTBW-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 1
- SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 0.000 description 1
- 108010014402 tyrosinase-related protein-1 Proteins 0.000 description 1
- 229940040064 ubiquinol Drugs 0.000 description 1
- QNTNKSLOFHEFPK-UPTCCGCDSA-N ubiquinol-10 Chemical compound COC1=C(O)C(C)=C(C\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)CCC=C(C)C)C(O)=C1OC QNTNKSLOFHEFPK-UPTCCGCDSA-N 0.000 description 1
- 229940035936 ubiquinone Drugs 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- NCYCYZXNIZJOKI-UHFFFAOYSA-N vitamin A aldehyde Natural products O=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-UHFFFAOYSA-N 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940075420 xanthine Drugs 0.000 description 1
- 235000008210 xanthophylls Nutrition 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 1
- GZWUQPQBOGLSIM-VOOUCTBASA-N γ msh Chemical compound C([C@H](N)C(=O)N[C@H](C(=O)N[C@@H](CCSC)C(=O)NCC(=O)N[C@@H](CC=1N=CNC=1)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC(O)=O)C(C)C)C1=CC=C(O)C=C1 GZWUQPQBOGLSIM-VOOUCTBASA-N 0.000 description 1
Classifications
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- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
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- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
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- A—HUMAN NECESSITIES
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- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
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- A—HUMAN NECESSITIES
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- Medicines Containing Plant Substances (AREA)
Description
基準(対照)として、およそ100本の毛髪を含有する一房を、頭皮の上できれいに切る。一房内の毛髪の色を、毛根近くの部分から毛先まで測定する。これは、1)目視でのスコア付けにより、2)高密度写真による記録およびスコア付けにより、3)髪の分解およびメラニン抽出に続く、色素分析および髪由来のメラニン含有量の決定により実施できる。この後者の場合、メラニンは、光度測定手段により、または化学反応(すなわち、ユーメラニンからのピロール−2,3,5トリカルボン酸の形成、およびフェオメラニンからのアミノヒドロキシフェニルアラニン異性体の形成と、それに続く定量的クロマトグラフィー、分光分析または分光光度分析)により測定され得る。
本発明に基づいて、ヘアケア組成物中に通常配合される、全ての公知の抗酸化剤が使用され得る。特に好ましいのは、アミノ酸(例えば、グリシン、ヒスチジン、チロシン、トリプトファン)およびそれらの誘導体;イミダゾール(例えば、ウロカニン酸)および誘導体;D,L−カルノシン、D−カルノシン、L−カルノシンなどのペプチドおよび誘導体(例えば、アンセリン);カロテノイド、カロテン(例えば、α−カロテン、β−カロテン、リコペン)および誘導体;クロロゲン酸および誘導体;リポ酸および誘導体(例えば、ジヒドロリポ酸);オーロチオグルコース、プロピルチオウラシル、およびその他のチオール(例えば、チオレドキシン(thioredoxine)、グルタチオン、システイン、シスチン、シスタミンおよびそのグリコシル−、N−アセチル−、メチル−、エチル−、プロピル−、アミル−、ブチル−およびラウリル−、パルミトイル−、オレイル−、y−リノリル−、コレステリル−、およびグリセリルエステル)、およびそれらの塩;ジラウリルチオジプロピオネート、ジステアリルチオジプロピオネート、ジチオジプロピオン酸、およびその誘導体(エステル、エーテル、ペプチド、脂質、ヌクレオチド、ヌクレオシド、および塩);ならびに非常に低い適合性用量(例えば、pmolからμmοl/kg)のスルホキシイミン化合物(ブチオニンスルホキシイミン、ホモシステインスルホキシイミン、ブチオニンスルホン、ペンタ−、ヘキサ−、ヘプタチオニンスルホキシイミンなど);それに加えて(金属)キレート剤(α−ヒドロキシ脂肪酸(クエン酸、乳酸、リンゴ酸)、パルミチン酸(palmic)、フィタン酸(phytinic acid)酸、ラクトフェリンなど)β−ヒドロキシ酸、フミン酸、没食子酸、没食子抽出物、ビリルビン、ビリベルジン、EDTA、EGTA、およびそれらの誘導体;不飽和脂肪酸およびそれらの誘導体(γ−リノール酸、リノール酸、オレイン酸など);葉酸およびその誘導体;ユビキノンおよびユビキノールおよびそれらの誘導体;ビタミンCおよび誘導体(パルミチン酸アスコルビルおよびテトライソパルミチン酸アスコルビル、Mg−リン酸アスコルビル、Na−リン酸アスコルビル、酢酸アスコルビルなど);トコフェロールおよび誘導体(酢酸ビタミンEなど);天然ビタミンE、ビタミンA、および誘導体(パルミチン酸ビタミンAおよび酢酸ビタミンA)の混合物;ならびに安息香酸コニフェリル、ルチン酸、および誘導体;α−グリコシルルチン;フェルラ酸;フルフリリデングルシトール;カルノシン;ブチルヒドロキシトルエン;ブチルヒドロキシアニソール;トリヒドロキシブチロフェノン;尿素およびその誘導体;マンノースおよび誘導体;亜鉛および誘導体(例えば、ZnO、ZnSO4);セレン(selen)および誘導体(例えば、セレノメチオニン);スチルベンおよび誘導体(スチルベンオキシド、トランス−スチルベンオキシドなど);および名前を挙げた活性成分の適切な誘導体(塩、エステル、エーテル、糖、ヌクレオチド、ヌクレオシド、ペプチドおよび脂質);あるいは超酸化物ジスムターゼ、カタラーゼなどの酵素、またはこのような酵素に類似した、またはこのような酵素賦活剤からなる群から選択される抗酸化剤である。1つまたは複数の保存料/抗酸化剤が、組成物の総重量の少なくとも0.01重量%の量で存在してもよい。好ましくは、本発明の組成物の総重量の約0.01重量%〜約10重量%で存在する。最も好ましくは、1つまたは複数の保存料/抗酸化剤が約0.1重量%〜約1重量%の量で存在する。
光遮蔽剤は、有利には、UV−A、UV−Bおよび/または広帯域フィルターから選択される。UV−Bまたは広域スペクトル遮蔽剤、すなわち約290〜340nmに吸収極大を有する物質の例は、有機または無機化合物であってもよい。有機UV−Bまたは広帯域遮蔽剤は、例えば、2−エチルヘキシル2−シアノ−3,3−ジフェニルアクリレート(オクトクリレン、PARSOL(登録商標)340)、エチル2−シアノ−3,3−−ジフェニルアクリレートなどのアクリレート;4−メチルベンジリデンショウノウ(PARSOL(登録商標)5000)、3−ベンジリデンショウノウ、ショウノウベンザルコニウムメトサルフェート、ポリアクリルアミドメチルベンジリデンショウノウ、スルホベンジリデンショウノウ、スルホメチルベンジリデンショウノウ、テレフタリデン二ショウノウスルホン酸などのショウノウ誘導体;メトキシケイ皮酸エチルヘキシル(PARSOL(登録商標)MCX)、メトキシケイ皮酸エトキシエチル、メトキシケイ皮酸ジエタノールアミン(PARSOL(登録商標)ヒドロ)、メトキシケイ皮酸イソアミルなどのケイ皮酸誘導体ならびにシロキサン結合ケイ皮酸誘導体;p−アミノ安息香酸、2−エチルヘキシルp−ジメチルアミノ安息香酸、Nーオキシプロピレン化p‐アミノ安息香酸エチル、p‐アミノ安息香酸グリセリルなどのp−アミノ安息香酸誘導体;ベンゾフェノン−3、ベンゾフェノン−4,2,2’,4,4’−テトラヒドロキシ−ベンゾフェノン、2,2’−ジヒドロキシ−4,4’−ジメトキシベンゾフェノンなどのベンゾフェノン;ジ−(2−エチルヘキシル)4−メトキシベンザルマロン酸などのベンザルマロン酸のエステル;欧州特許第0895776号明細書に記載されるような2−(4−エトキシアニリノメチレン)プロパン二酸ジエチルエステルなどの2−(4−エトキシ−アニリノメチレン)プロパン二酸のエステル;ポリシリコーン−15(PARSOL(登録商標)SLX)などの欧州特許第0358584B1号明細書、欧州特許第0538431B1号明細書、および欧州特許公開第0709080A1号明細書に記載されるようなベンズマロネート基含有オルガノシロキサン化合物;ドロメトリゾールトリシロキサン(メキソリルXL);例えば、2−フェニルベンゾイミダゾールスルホン酸およびその塩(PARSOL(登録商標)HS)などのイミダゾール誘導体である。2−フェニルベンゾイミダゾールスルホン酸の塩は、例えば、ナトリウムまたはカリウム塩、アンモニウム塩、モルホリン塩、モノエタノールアミン塩、ジエタノールアミン塩などのような一級、二級、および三級アミンの塩などのアルカリ塩;サリチル酸イソプロピルベンジル、サリチル酸ベンジル、サリチル酸ブチル、サリチル酸エチルヘキシル(PARSOL(登録商標)EHS、NEO Heliopan OS)、サリチル酸イソオクチルまたはサリチル酸ホモメンチル(ホモサラート、PARSOL(登録商標)HMS、NEO Heliopan OS)などのサリチル酸誘導体;エチルヘキシルトリアゾン(Uvinul T−150)、ジエチルヘキシルブタミドトリアゾン(Uvasorb HEB)などのトリアジン誘導体、カプセル化メトキシケイ皮酸エチルヘキシル(Eusolex UV−pearls)または例えば、欧州特許第1471995号明細書で開示されるUV−フィルター装填マイクロカプセルなどのカプセル化UV−フィルターである。無機化合物は、微粒子化されたTiO2、ZnOなどの顔料である。「微粒子化された」という用語は、約5nm〜約200nm、特に約15nm〜約100nmの粒度を指す。TiO2粒子はまた、例えば、アルミニウムまたはジルコニウム酸化物などの金属酸化物により、または例えば、ポリオール、メチコン、ステアリン酸アルミニウム、アルキルシランなどの有機コーティングにより、被覆されてもよい。このようなコーティングは、当該技術分野で周知である。
本発明に基づいて、ヘアケア組成物中に通常配合される、電磁放射線の可視光(400nm〜800nm)に吸収を有する着色剤は、全て使用され得る。吸収は、アゾ−(モノ−、ジ−、トリス−、またはポリ−)スチルベン−、カロテノイド(carotenoide)−、ジアリールメタン−、トリアリールメタン−、キサンテン−、アクリジン−、キノリン−、メチン−(ポリメチン−もまた)チアゾール−、インダミン−、インドフェノール−、アジン−、オキサジン−、チアジン−、アントラキノン−、インジゴ−、フタロシアニン(phthalocyanin)、およびさらなる合成、天然および/または無機発色団の発色団によって引き起こされることが多い。
生物活性物質は、有利には、チロシナーゼ賦活剤のようなメラニン形成の一般的賦活剤、ペプチドホルモン、cAMP賦活剤、およびニューロトロフィンから選択される。
ヘアケア組成物は、好ましくは、
1.)水
2.)好ましくはC1〜C4アルカノールである、水溶性有機溶媒
3.)油、脂肪性物質、ワックス
4.)3)とは異なる、一価、二価または三価のアルコールとC6〜C30モノカルボン酸との様々なエステル
5.)飽和非環式および環式炭化水素
6.)脂肪酸
7.)脂肪アルコール
8.)シリコーン油
9.)界面活性成分
およびそれらの混合物から選択される、追加的な美容のまたは皮膚科補助剤および/または添加剤(化粧品担体)を含み得る。
1.0.1〜20重量%、好ましくは1〜10重量%の少なくとも1つのヘアポリマー;
2.C2−C5アルコールから選択され、好ましくはエタノールである、0〜10重量%の少なくとも1つの担体(溶媒);
3.0.01〜5重量%、好ましくは0.2〜3重量%の少なくとも1つの増粘剤;
4.0〜50重量%の噴霧剤;
5.0〜10重量%、好ましくは0.1〜3重量%の1.)とは異なる、好ましくは水溶性非イオン性ポリマーである、スタイリングポリマー;
6.好ましくはグリセリンおよびグリセリン誘導体から選択される、0〜1重量%の少なくとも1つの再脂肪化剤;
7.例えば、シリコーン成分である、0〜30重量%のその他の通例の添加剤;
8.0.005〜5重量%の本発明によるエーデルワイス抽出物;
9.100重量%になる量の水
を含み得る。
1.0.05〜10重量%のヘアポリマー
2.5〜95重量%の水
3.5〜50重量%の界面活性剤
4.0〜5重量%の追加的なコンディショニング剤
5.0〜10重量%のその他の通例の添加剤
6.20重量%までのエーデルワイス抽出物
を含んでもよく、全成分を合わせると100重量%になる。
1.0.1〜10重量%の少なくとも1つのヘアポリマー;
2.20〜99重量%の水および/またはアルコール;
3.0〜70重量%の少なくとも1つの噴霧剤;
4.0〜20重量%の通例の添加剤;
5.0.005〜5重量%の本発明によるエーデルワイス抽出物
を含み得る。
1.0.1〜10重量%のヘアポリマー;
2.60〜99.85重量%の水および/またはアルコール;
3.0.05〜10重量%のゲル形成剤;
4.0〜20重量%のその他の通例の添加剤;
5.0.005〜5重量%の本発明によるエーデルワイス抽出物
を含み得る。
1.0.005〜5重量%の本発明によるエーデルワイス抽出物;
2.水、水混和性溶媒、およびそれらの混合物から選択される、30〜99.5重量%、好ましくは40〜99重量%の少なくとも1つの溶媒;
3.0〜70重量%の噴霧剤;
4.0.1〜10重量%の少なくとも1つの水溶性または水分散性ヘアポリマー;
5.0〜0.3重量%の少なくとも1つの水不溶性シリコーン;
6.好ましくは少なくとも1つの脂肪酸アミドである、0〜0.5重量%の少なくとも1つのワックス;
7.通例の添加剤
を含み得る。
1.0.05〜20重量%の少なくとも1つのヘアポリマー;
2.20〜99.95重量%の水および/またはアルコール;
3.0〜79.5重量%の通例の添加剤;
4.0.005〜5重量%の本発明によるエーデルワイス抽出物
を含み得る。
1.0.1〜10重量%の少なくとも1つのヘアポリマー;
2.55〜99.8重量%の水および/またはアルコール;
3.5〜20重量%の噴霧剤;
4.0.1〜5重量%の乳化剤;
5.0〜10重量%の通例の添加剤;
6.0.005〜5重量%の本発明によるエーデルワイス抽出物
を含み得る。
1.0.05〜10重量%のヘアポリマー;
2.25〜94.95重量%の水;
3.5〜50重量%の界面活性剤;
4.0〜5重量%の追加的なコンディショニング剤
5.0〜10重量%のその他の通例の添加剤;
6.0.005〜5重量%の本発明によるエーデルワイス抽出物;
7.0〜5重量%の乳白剤および/または真珠光沢付与物質
を含み得る。
[実施例1:培養されたヒト毛嚢中の遺伝子発現に対するエーデルワイス抽出物の効果]
[1−材料および方法]:
A)試験材料および調製品:5重量%乾燥残留物の濃度のエーデルワイス抽出物(DSMからのALPAFLOR(登録商標)エーデルワイス)が、60%エタノール中の原液として調製された。原液は、細胞培養液中で最終試験濃度に希釈された。
培養条件:37℃、5%CO2
培養液:ペニシリン50U/ml、ストレプトマイシン50μg/ml、L−グルタミン2mM、インスリン10μg/ml、ヒドロコルチゾン0.004μg/mlを添加したウイリアムスE培地
条件あたり13個の高品質毛球毛髪鱗茎が72時間培養された。培養の終了時に、毛球は液体窒素中で即座に冷凍されて、RNA抽出のために−80℃で保存された。
各処理について細胞単層から抽出されたmRNA上で、RT−qPCR方法を使用して、選択された遺伝子の発現が解析された。RNA抽出前に、レプリカがプールされた。次に、遺伝子発現の解析が、二重反復試験(n=2)で実施された。
逆転写:TriPure溶液試薬を使用して、供給業者の勧告に従って、全RNAが各サンプルから抽出された。ラボ・オン・チップ・バイオアナライザ(Agilent Technologies)を使用して、RNAの量および質が評価された。ゲノムDNAの可能な汚染物質痕跡は、DNAfreeシステム(Ambion)を使用して除去された。RNAの量は、Nanovue(GE Healthcare)を使用して評価された。mRNAの逆転転写は、オリゴ(dT)およびSuperscript II逆転写酵素(Invitrogen)の存在下で実施された。Nanovueはまた、cDNA定量化およびDNA濃度調節でも使用された。
定量PCR:PCR(ポリメラーゼ鎖反応)は、Light Cyclerシステム(Roche Molecular Systems Inc.)を使用して、供給業者の取扱説明書に従って実施された。このシステムは、試験プライマーの解析条件決定後の迅速なおよび強力なPCRを可能にする。反応混合物は、希釈DNA、順方向および逆方向プライマー、taqDNAポリメラーゼ含有試薬混合物、SYBRグリーンIおよびMgCl2を含有する。増幅DNA中への蛍光の組み込みが、PCRサイクル中に連続的に測定された。これは、PCRサイクルプロットに対する蛍光強度をもたらして、各遺伝子の相対的発現(RE)値の評価を可能にした。RE計算のために選択された値は、蛍光曲線の出力点(Ct)である。検討される遺伝子では、サイクル数が高いほど、mRNA量は低くなる。RE値は、式、(サイクル数の1/2)×106に従って、任意の単位(AU)で表される。追加的な対照のために、本発明者らは、未処理対照細胞と処理細胞の双方で、3つのハウスキーピング遺伝子、すなわちリボソームタンパク質S28、グリセルアルデヒド−3−リン酸デヒドロゲナーゼ、およびβアクチンの発現レベルもまた定量化した。3つのハウスキーピング遺伝子の平均相対発現レベルは、100%に設定されて、個々の3つの遺伝子の発現レベルの変動は、100±50%未満以内であった。
表1に要約されるように、エーデルワイス抽出物は、以下の重要なメラニン形成マーカーの遺伝子発現を調節した。
チロシナーゼ:メラニン合成中の2つの反応(チロシンおよびL−Dopaの酸化)を触媒する、重要な律速酵素。
チロシナーゼ−関連タンパク質1:Tyrp1は、メラニン合成に関与するメラノサイト−特異的遺伝子産物である。マウスTyrp1がジヒドロキシインドールカルボン酸オキシダーゼ活性を有する一方で、ヒトメラノサイト中の機能は、あまり明らかでない。メラニン合成におけるその役割に加えて、Tyrp1は、チロシナーゼタンパク質の安定化に関与して、その触媒活性を調節する。Tyrp1はまた、メラノソーム構造の維持に関与して、メラノサイト増殖およびメラノサイト細胞死に影響を及ぼす。(Wikipediaより)
シルバーホモログ:メラノソームのマーカー。
無傷の色素性ユニットがある毛嚢の最適な品質のために、Philpottおよび同僚により発表されたプロトコル(Philpott et al.1990,Philpott 1999)をわずかに変更したものに従って、髪周期の成長期VIにある正常なヒトの頭皮皮膚毛嚢を単離した。簡単に述べると、切開用双眼顕微鏡により皮下脂肪から表皮および真皮を分離した後、真皮/皮下組織境界の直上の真皮、皮下脂肪中に位置する発育期毛包の近位の3分の2を、時計修理用ピンセットを使用して単離し、引き続いて、完全毛嚢培地(Williams E,Biochrom KG seromed,ドイツ国ベルリン(Berlin,Germany));1%ペニシリン−ストレプトマイシン(Life Technologies,ドイツ国エッゲンシュタイン(Eggenstein,Germany));1%L−グルタミン200mM(Life Technologies,ドイツ国エッゲンシュタイン);0.02%ヒドロコルチゾン(Sigma,ドイツ国タウフキルヘン(Taufkirchen,Germany));0.1%インスリン(Sigma,ドイツ国タウフキルヘン)を含有するペトリ皿内に収集した。次に、ウェルあたり3つの毛嚢をランダムに分配し、ウェルあたり500mlの完全毛嚢培地を含む24ウェルプレート(Costar,米国ニューヨーク(NY,USA))で培養した。
Claims (8)
- 白髪化を防止するためのエーデルワイス抽出物を含む局所用ヘアケア組成物(但し、タウリン、メチオニン、ヒスチジンまたは7−オキソ−DHEA誘導体を含む組成物を除く)の使用であって、
前記局所用ヘアケア組成物が、前記局所用ヘアケア組成物の総重量を基準にして、0.001重量%〜1重量%のエーデルワイス抽出物を含み、
前記エーデルワイス抽出物が、セイヨウウスユキソウの気中部分を熱気流下で乾燥し、続いてミル粉砕し、得られた乾燥植物をエタノール水溶液で抽出し、次にエタノールを真空蒸留によって除去し、得られた濃縮物をグリセリンまたはグルセリンとエタノールの混合物で希釈することにより調製された抽出物である、使用。 - 前記局所用ヘアケア組成物が、抗酸化剤、光遮蔽剤、および/または毛髪着色剤をさらに含む、請求項1に記載の使用。
- 前記局所用ヘアケア組成物が、ヘアトニック、コンディショナー、トリートメント、またはスタイリングジェルである、請求項1または2に記載の使用。
- 前記局所用ヘアケア組成物が、1日あたり少なくとも2回塗布される、請求項1〜3のいずれか一項に記載の使用。
- エーデルワイス抽出物の有効量を含む局所用組成物(但し、タウリン、メチオニン、ヒスチジンまたは7−オキソ−DHEA誘導体を含む組成物を除く)をヒト毛髪を有する皮膚に塗布するステップを含む、白髪化を防止する方法であって、
前記エーデルワイス抽出物の有効量が、前記局所用組成物の総重量を基準にして、0.001重量%〜1重量%の範囲で選択され、
前記エーデルワイス抽出物が、セイヨウウスユキソウの気中部分を熱気流下で乾燥し、続いてミル粉砕し、得られた乾燥植物をエタノール水溶液で抽出し、次にエタノールを真空蒸留によって除去し、得られた濃縮物をグリセリンまたはグルセリンとエタノールの混合物で希釈することにより調製された抽出物である、方法。 - 前記局所用組成物がヘアケア組成物である、請求項5に記載の方法。
- 前記ヘアケア組成物が、ヘアトニック、コンディショナー、トリートメント、またはスタイリングジェルである、請求項6に記載の方法。
- 前記局所用組成物が、抗酸化剤、光遮蔽剤、および着色剤からなる群から選択される少なくとも1つの追加的な活性物質をさらに含む、請求項5〜7のいずれか一項に記載の方法。
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EP20130193397 EP2873414A1 (en) | 2013-11-19 | 2013-11-19 | Use of an edelweiss extract in hair care for the prevention of hair graying |
EP13193397.0 | 2013-11-19 | ||
PCT/EP2014/074780 WO2015074997A1 (en) | 2013-11-19 | 2014-11-17 | Use of an edelweiss extract in hair care for the prevention of hair graying |
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JP2016537350A JP2016537350A (ja) | 2016-12-01 |
JP6631805B2 true JP6631805B2 (ja) | 2020-01-15 |
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US (1) | US20160271195A1 (ja) |
EP (2) | EP2873414A1 (ja) |
JP (1) | JP6631805B2 (ja) |
KR (1) | KR102327760B1 (ja) |
CN (1) | CN105744928A (ja) |
BR (1) | BR112016011184B1 (ja) |
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WO (1) | WO2015074997A1 (ja) |
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KR102406640B1 (ko) * | 2015-09-30 | 2022-06-08 | (주)아모레퍼시픽 | 두피와 모발의 노화지수 산출방법 |
WO2017182401A1 (en) * | 2016-04-20 | 2017-10-26 | L'oreal | Cosmetic composition comprising a particular combination of surfactants, a polyol, a cationic or amphoteric polymer and optionally a silicone. |
EP3296961A1 (en) * | 2016-09-16 | 2018-03-21 | Noxell Corporation | Calculating a composition for a preparation for treating hair fibers |
JP6994970B2 (ja) * | 2018-02-08 | 2022-01-14 | 株式会社サニープレイス | ヘアカラー方法 |
WO2020002523A1 (en) * | 2018-06-28 | 2020-01-02 | L'oreal | Cosmetic composition comprising surfactants, a polymer comprising at least one (meth)acrylic unit and a silicone |
CN109363978B (zh) * | 2018-12-28 | 2021-07-20 | 汕头市润晶化妆品有限公司 | 温和天然植物护发素及其制备方法 |
KR102150716B1 (ko) | 2019-12-18 | 2020-09-01 | (주)웰포트 | 주사기 일체형 혈소판 추출기구 |
CN114028275B (zh) * | 2021-12-16 | 2022-11-29 | 四川大学 | 香皂催化黑色素聚合的染发剂、其制备方法及使用方法 |
DE102022109519A1 (de) | 2022-04-20 | 2023-10-26 | Güven Öztürk | Haarpflegemittel auf Pflanzenbasis |
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- 2014-11-17 CN CN201480062902.6A patent/CN105744928A/zh active Pending
- 2014-11-17 ES ES14802843T patent/ES2775212T3/es active Active
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BR112016011184A2 (pt) | 2017-09-12 |
BR112016011184B1 (pt) | 2020-07-14 |
JP2016537350A (ja) | 2016-12-01 |
ES2775212T3 (es) | 2020-07-24 |
EP2873414A1 (en) | 2015-05-20 |
KR20160086336A (ko) | 2016-07-19 |
KR102327760B1 (ko) | 2021-11-17 |
EP3071180B1 (en) | 2019-12-25 |
WO2015074997A1 (en) | 2015-05-28 |
US20160271195A1 (en) | 2016-09-22 |
EP3071180A1 (en) | 2016-09-28 |
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