JP2015160821A - 美白用組成物及び化粧料 - Google Patents
美白用組成物及び化粧料 Download PDFInfo
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- JP2015160821A JP2015160821A JP2014036035A JP2014036035A JP2015160821A JP 2015160821 A JP2015160821 A JP 2015160821A JP 2014036035 A JP2014036035 A JP 2014036035A JP 2014036035 A JP2014036035 A JP 2014036035A JP 2015160821 A JP2015160821 A JP 2015160821A
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- extract
- acid
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- cosmetics
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Landscapes
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Abstract
Description
本発明は、マタタビ科(Actinidiaceae)マタタビ属(Actinidia)のキウイの果実の抽出物と美白剤とを含有する美白用組成物、及び当該組成物を配合した化粧料である。
なお、本明細書において化粧料なる文言は、所謂化粧料のほかに医薬部外品までも含む広義で用いる。
キウイ(Actinidia chinensis)の未成熟果実300gをミンチ状にし、これに精製水50gを添加する。この精製水により冷蔵で一晩抽出を行う。抽出液を濾過し、淡褐色透明のキウイの未成熟果実抽出物300g(固形分濃度 2.0%)を得た。
[A成分] 部
流動パラフィン 5.0
パラフィン 5.0
グリセリルモノステアレート 2.0
ポリオキシエチレン(20)ソルビタンモノステアレート 6.0
フェノキシエタノール 0.1
[B成分] 部
製造例1の抽出物溶液 2.5
グリセリン 5.0
カルボキシメチルモノステアレート 0.1
精製水 全量が100部となる量
[C成分]
香料 適量
上記のA成分とB成分をそれぞれ80℃以上に加熱した後、攪拌混合した。これを50℃まで冷却した後、C成分を加えてさらに攪拌混合してクリームを得た。
[A成分] 部
流動パラフィン 6.0
オリーブ油 1.0
ポリオキシエチレン(20)ソルビタンモノステアレート 2.0
大豆レシチン 1.5
メチルパラベン 0.15
[B成分] 部
製造例1の抽出物溶液 2.0
タケノコの皮の抽出物溶液 2.0
グリセリン 3.0
1、3−ブチレングリコール 2.0
カルボキシメチルセルロース 0.3
コラーゲン 0.1
精製水 全量が100部となる量
[C成分]
香料 適量
上記のA成分とB成分をそれぞれ80℃以上に加熱した後、攪拌混合した。これを50℃まで冷却した後、C成分を加えてさらに攪拌混合して乳液を得た。
[A成分] 部
製造例1の抽出物溶液 2.0
エタノール 10.0
グリセリン 3.0
1、3−ブチレングリコール 2.0
フェノキシエタノール 0.2
クエン酸 0.1
クエン酸ナトリウム 0.3
カルボキシビニルポリマー 0.1
香料 適量
水酸化カリウム 適量
精製水 全量が100部となる量
上記の成分を混合してローションを得た。
[A成分] 部
オリーブ油 1.0
ポリオキシエチレン(5.5)セチルアルコール 5.0
[B成分] 部
製造例1の抽出物溶液 5.0
モモの未成熟果実の抽出物溶液 2.0
エタノール 5.0
グリセリン 5.0
1,3−ブチレングリコール 5.0
水酸化カリウム 適量
精製水 全量が100部となる量
[C成分] 部
香料 適量
A成分及びB成分をそれぞれ80℃以上に加温後、A成分にB成分を加えて攪拌し、さらにヒスコトロン(5000rpm)で2分間ホモジナイズを行った。これを50℃まで冷却した後、C成分を加えて攪拌混合し、さらに30℃以下まで冷却して化粧水を得た。
[A成分] 部
流動パラフィン 6.0
ホホバ油 1.0
ポリオキシエチレン(20)ソルビタンモノステアレート 2.0
大豆レシチン 1.5
メチルパラベン 0.15
エチルパラベン 0.03
[B成分]
製造例1の抽出物溶液 5.0
L−アスコルビン酸−2−グルコシド 2.0
水酸化カリウム 0.5
グリセリン 3.0
1、3−ブチレングリコール 2.0
カルボキシメチルセルロース 0.3
ヒアルロン酸ナトリウム 0.01
精製水 全量が100部となる量
[C成分]
香料 適量
上記のA成分とB成分をそれぞれ80℃以上に加熱した後、攪拌混合した。これを50℃まで冷却した後、C成分を加えてさらに攪拌混合して乳液を得た。
実施例5のB成分中、L−アスコルビン酸−2−グルコシド2.0部及び水酸化カリウム0.5部に代えてL−アスコルビン酸−2−リン酸エステルマグネシウム2.0部を用いるほかは実施例と同様にして乳液を得た。
実施例5のB成分中、L−アスコルビン酸−2−グルコシド2.0部及び水酸化カリウム0.5部に代えてトラネキサム酸2.0部を用いるほかは実施例5と同様にして乳液を得た。
実施例5のB成分中、L−アスコルビン酸−2−グルコシド2.0部及び水酸化カリウム0.5部に代えてアルブチン2.0部を用いるほかは実施例5と同様にして乳液を得た。
[A成分] 部
流動パラフィン 6.0
ホホバ油 1.0
ポリオキシエチレン(20)ソルビタンモノステアレート 2.0
大豆レシチン 1.5
メチルパラベン 0.15
エチルパラベン 0.03
[B成分]
製造例1の抽出物溶液 5.0
L−アスコルビン酸−2−グルコシド 2.0
アルブチン 3.0
水酸化カリウム 0.5
グリセリン 3.0
1、3−ブチレングリコール 2.0
カルボキシメチルセルロース 0.3
ヒアルロン酸ナトリウム 0.01
精製水 全量が100部となる量
[C成分]
香料 適量
上記のA成分とB成分をそれぞれ80℃以上に加熱した後、攪拌混合した。これを50℃まで冷却した後、C成分を加えてさらに攪拌混合して乳液を得た。
[A成分] 部
ステアリン酸 2.4
モノステアリン酸プロピレングリコール 2.0
セトステアリルアルコール 0.2
液状ラノリン 2.0
流動パラフィン 3.0
ミリスチン酸イソプロピル 8.5
プロピルパラベン 0.05
[B成分]
製造例1の抽出物溶液 2.0
カルボキシメチルセルロースナトリウム 0.2
ベントナイト 0.5
プロピレングリコール 4.0
トリエタノールアミン 1.1
メチルパラベン 0.1
精製水 全量が100部となる量
[C成分]
酸化チタン 8.0
タルク 4.0
着色顔料 適量
上記のA成分とB成分をそれぞれ加温した後混合攪拌した。これを再加温し、上記のC成分を添加して型に流し込み、室温になるまで攪拌してリキッドファンデーションを得た。
[A成分] 部
ステアリン酸 5.0
セタノール 2.0
モノステアリン酸グリセリル 3.0
流動パラフィン 5.0
スクワラン 3.0
ミリスチン酸イソプロピル 8.0
ポリオキシエチレン(20)モノステアリン酸グリセリル 2.0
プロピルパラベン 0.1
[B成分] 部
製造例1の抽出物溶液 2.5
ソルビトール 3.0
1,3−ブチレングリコール 5.0
トリエタノールアミン 1.5
メチルパラベン 0.1
精製水 全量が100部となる量
[C成分] 部
酸化チタン 8.0
タルク 2.0
カオリン 5.0
ベントナイト 1.0
着色顔料 適量
[D成分] 部
香料 0.3
C成分を混合し、粉砕機で粉砕した。B成分を混合し、これに粉砕したC成分を加え、コロイドミルで均一分散させた。A成分及び均一分散させたB、C成分をそれぞれ80℃に加温後、B、C成分にA成分を攪拌しながら加え、さらにヒスコトロン(5000rpm)で2分間ホモジナイズを行った。これを50℃まで冷却した後、D成分を加えて攪拌混合し、さらに攪拌しながら30℃以下まで冷却してクリームファンデーションを得た。
[A成分] 部
N−ラウロイルメチルアラニンナトリウム 25.0
ヤシ油脂肪酸カリウム液(40%) 26.0
ヤシ油脂肪酸ジエタノールアミド 3.0
メチルパラベン 0.1
[B成分] 部
製造例1の抽出物溶液 5.0
1,3−ブチレングリコール 2.0
精製水 全量が100部となる量
A成分及びB成分をそれぞれ80℃に加温して均一に溶解した後、A成分にB成分を加え、攪拌を続けて室温まで冷却してボディシャンプーを得た。
[A成分] 部
N−ヤシ油脂肪酸メチルタウリンナトリウム 10.0
ポリオキシエチレン(3)アルキルエーテル硫酸ナトリウム 20.0
ラウリルジメチルアミノ酢酸ベタイン 10.0
ヤシ油脂肪酸ジエタノールアミド 4.0
メチルパラベン 0.1
[B成分]
クエン酸 0.1
製造例1の抽出物 2.0
1,3−ブチレングリコール 2.0
精製水 全量が100部となる量
A成分及びB成分をそれぞれ80℃に加温して均一に溶解した後、A成分にB成分を加え、攪拌を続けて室温まで冷却してヘアシャンプーを得た。
[A成分] 部
ポリオキシエチレン(10)硬化ヒマシ油 1.0
塩化ジステアリルジメチルアンモニウム 1.5
塩化ステアリルトリメチルアンモニウム 2.0
2−エチルヘキサン酸グリセリル 1.0
セタノール 3.2
ステアリルアルコール 1.0
メチルパラベン 0.1
[B成分]
製造例1の抽出物 2.0
1,3−ブチレングリコール 5.0
精製水 全量が100部となる量
A成分及びB成分をそれぞれ80℃に加温して均一に溶解した後、A成分にB成分を加え、攪拌を続けて室温まで冷却してヘアリンスを得た。
製造例1の抽出物 10.0
コラーゲン 8.0
クエン酸 0.1
甘味料(スクロース) 0.01
酸化防止剤(ビタミンC)0.01
精製水 全量が100部となる量
製造例1の抽出物 20.0
ビタミンC 20.0
脂肪酸エステル 10.0
乳酸カルシウム 20.0
乳糖 30.0
上記重量部の各成分を混合した後、加圧成形し、錠剤とした。
[試験方法]
培養B16マウスメラノーマ細胞を、96穴マイクロプレートに8×103個/穴播種し、10%仔牛血清(FBS)含有RPMI培地中、37℃、5%CO2の条件下に1日間プレ培養した後、10%FBS含有RPMI培地に本発明の製造例1に係る抽出物を試料溶液として添加し、同条件で2日間培養した。ここで、本試験で用いた試料溶液としての濃度は、当該培地に対して溶液としての終濃度が1.0,2.0重量%となるように調製した。次に培養液を除去し、界面活性剤(Triton X-100)と5mMのL−ドーパ溶液を添加して37℃で反応を行った後、マイクロプレートリーダー(Model 450、バイオラッド社製)を用い、波長490nmでドーパ値を測定した。試料溶液に代えてPBS(‐)溶液(Control)を用いた場合についても上記と同様の操作を行い、ここに得られたドーパ値に対する各試料添加時のドーパ値の相対値を求め、チロシナーゼ活性率(%)とした。さらに、本発明の製造例1に係る抽出物と美白剤[アスコルビン酸 2−グルコシド(0.05%)]を試料溶液として用いた場合についても同様の操作を行い、チロシナーゼ活性率(%)を算出した。また、比較対象として、試料溶液に代えてアスコルビン酸 2−グルコシド(0.05%)を用いた場合についても同様の操作を行い、チロシナーゼ活性率(%)を算出した。
[表1]
[試験方法]
培養B16メラノーマ細胞を、フラスコに5.0×105個播種し、10%FBS含有RPMI培地中、37℃、5%CO2の条件下でプレ培養を行った後、10%FBS含有RPMI培地で本発明の製造例1に係る抽出物を希釈した液に交換し、同条件で3日間培養した。ここで、本試験で用いた試料溶液としての濃度は、当該培地に対して溶液としての終濃度が1.0,2.0重量%となるように調製した。次に、培養液を除去し、細胞を回収した後、0.1N NaOH含有10%DMSO溶液を加えて細胞内容物を抽出した。この抽出液について、分光光度計(U-2000、株式会社日立製)を用い波長475nmでメラニン量を、又プロテインアッセイキット(バイオラッド社製)でタンパク質量を測定した。ここに得られた結果から、タンパク質量当たりのメラニン量を算出した。試料溶液に代えてコントロールとしてPBS(‐)を添加したときのメラニン量も測定し、当該メラニン量を100としたときの試料添加時の当該メラニン量の相対値をメラニン生成率(%)として表した。さらに、本発明の製造例1に係る抽出物と美白剤[アスコルビン酸 2−グルコシド(0.05%)]を試料溶液として用いた場合についても同様の操作を行い、メラニン生成率(%)を算出した。また、比較対象として、試料溶液に代えてアスコルビン酸 2−グルコシド(0.05%)を用いた場合についても同様の操作を行い、メラニン生成率(%)を算出した。
[表2]
正常ヒト表皮メラニン細胞を増殖添加剤含有DermaLife(登録商標)「クラボウ社製」にて1×105個/mLに調製し、96穴マイクロプレートに100μLずつ播種して、5%炭酸ガス、飽和水蒸気下、37℃で培養した。24時間後、本発明の製造例1に係る抽出物を試料溶液として含んだ培養液を追添加しさらに培養した。ここで、試料溶液は、培養液に対する溶液としての終濃度が1.0%,2.0%となるように調製した。また、コントロールとして、試料溶液に代えてPBS(−)を含んだ培養液を追添加した対照区を設定した。なお、PBS(‐)は、試料溶液と同様に溶液としての培養液に対して終濃度2.0%となるように調製した。48時間後、培養上清を除去して、PBS(−)を200μLずつ添加して除去し、次に10%トリクロロ酢酸(和光純薬社)を50μLずつ添加して冷温下で30分間インキュベートした後、上清を除去した。PBS(−)を100μL用いて洗浄し、0.2%Triton-X含有PBS(−)を50μLずつ添加して室温下で1時間インキュベートをした。上清を除去して8%牛血清アルブミン(SIGMA社)含有PBS(−)を50μLずつ添加して室温下で2時間インキュベートした。上清を除去し0.2%Triton-X含有PBS(−)を100μL用いて洗浄し、抗SVCTマウスモノクローナル抗体(Santa Cruz社)を50μLずつ添加して冷温下で24時間インキュベートした。上清を除去し0.2%Triton-X含有PBS(−)100μLを用いて洗浄を3回繰り返した。Alexa Fluor 488抗マウス二次抗体(Life Technologies社)を50μL添加して室温下、暗所にて2時間インキュベートした。上清を除去し0.2%Triton-X含有PBS(−)100μLを用いて洗浄を3回繰り返し、PBS(−)を100μLずつ添加して蛍光プレートリーダー(大日本製薬社)を用いてEx485/Em520における蛍光強度を測定した。対照区の測定値に対する蛍光強度の相対値をSVCT合成率(%)とした。
[表3]
正常ヒト表皮細胞を、96穴マイクロプレートに1×104個/穴播種した。培地は、Humedia KG2(クラボウ社製)を加えたものを用いた。これを37℃,5.0%CO2の条件下に3日間プレ培養した後、本発明の製造例1に係る抽出物を試料溶液として培地に添加し、同条件でさらに4日間培養した。ここで、試料溶液は、培養液に対する溶液としての終濃度が1.0%,2.0%となるように調製した。次に、培地を除去し、PBS(-)で洗浄した後、PMSF含有1%TritonX−100溶液を添加し、細胞の溶解操作を行ったものを酵素溶液とした。次いで、基質溶液(1mMの4‐Methylumbelliferyl-β-Glucopyranoside)を加え、ボルテックスミキサーで穏やかに攪拌しながら37℃で1時間反応させた。反応停止液(0.2M carbonate bicarbonate buffer(pH10.5))を加えて反応停止させた後、蛍光強度(励起:355nm、放射:460nm:蛍光マイクロプレートリーダー(フルオロスキャンアセント、Thermo Fisher Scientific社製))を測定した。また、コントロールとして試料溶液に代えてPBS(-)を添加した場合(対照区)についても上記と同様の操作を行い、ここに得られた蛍光強度に対する各試料添加時の蛍光強度の相対値を求め、表皮細胞内のβ-グルコセレブロシダーゼ活性亢進率(%)とした。
[表4]
Claims (4)
- マタタビ科(Actinidiaceae)マタタビ属(Actinidia)のキウイの果実の抽出物を有効成分とする美白用組成物。
- マタタビ科(Actinidiaceae)マタタビ属(Actinidia)のキウイの果実の抽出物と美白剤とを含有する美白用組成物。
- マタタビ科(Actinidiaceae)マタタビ属(Actinidia)のキウイの果実の抽出物を有効成分とする保湿用組成物。
- 請求項1から3のいずれか一項に記載の組成物を含む化粧料。
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