JP6506695B2 - 化粧品組成物 - Google Patents
化粧品組成物 Download PDFInfo
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- JP6506695B2 JP6506695B2 JP2015548176A JP2015548176A JP6506695B2 JP 6506695 B2 JP6506695 B2 JP 6506695B2 JP 2015548176 A JP2015548176 A JP 2015548176A JP 2015548176 A JP2015548176 A JP 2015548176A JP 6506695 B2 JP6506695 B2 JP 6506695B2
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- 239000002537 cosmetic Substances 0.000 title claims description 34
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- -1 iron oxide Chemical compound 0.000 claims description 46
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- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 8
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 8
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
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- 238000003384 imaging method Methods 0.000 description 3
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- FSEXLNMNADBYJU-UHFFFAOYSA-N 2-phenylquinoline Chemical compound C1=CC=CC=C1C1=CC=C(C=CC=C2)C2=N1 FSEXLNMNADBYJU-UHFFFAOYSA-N 0.000 description 2
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Landscapes
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- Inorganic Chemistry (AREA)
- Emergency Medicine (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dermatology (AREA)
- Zoology (AREA)
- Gerontology & Geriatric Medicine (AREA)
- Cosmetics (AREA)
Description
耐洗い流し性/耐摩耗性試験
1.較正曲線の作成
ベース処方物(表1のサンプルA)をバイオスキンプレート(色:30#、日本、東京のビューラックス社より)上に、0、0.5、1、1.5、2、2.5、3、3.5、4、5および6mg/cm2の表面密度で均一にコーティングした。およそ25℃で8時間自然乾燥させた後、これらのコーティングしたバイオスキンプレートのL(明度に関して)、aおよびb(反対色次元に関して)を、デジアイ・イメージング・システム(Verivide、英国)を使用して測定した。ITA値を式ITA=[arctan(L−50/b)]×180/πによって計算した。次にITA値対表面密度をプロットし、多項式モデルに当てはめて曲線を得た。Rの二乗は0.999より大きく、多項式モデルがベース処方物の明度と表面密度との間の関数関係への当てはめに好適であることを示した。
サンプル30mgをバイオスキンプレート上に、10cm2の面積で均一にコーティングした。コーティングしたバイオスキンをおよそ25℃で8時間自然乾燥させた。バイオスキンプレートのL、aおよびbをデジアイ・イメージング・システム(Verivide、英国)を使用して測定した。ITA値(ITA1)を上の式に従って計算した。較正曲線に従って、洗い流し/摩耗性試験前の表面密度値(SD1)を得た。コーティングしたバイオスキンを脱イオン水に30秒間浸漬した。次に、市販の洗顔剤(ポンズ・ゴールド・ラディアンス(商標)ラディアンス・ブースティング・クレンジング・ムース)を5mg/cm2の量でバイオスキンプレートに適用し、コーティングされたバイオスキンプレートをマーチンデール摩耗性およびピリング試験機(型番:M235、SDL Altas、米国)によって、33.72gのモーションプレートを用いて、30rpmの速度で1分間洗浄した。続いて、コーティングしたバイオスキンプレートをさらに1分間水に浸漬して、脱イオン水で洗浄した。およそ25℃で2時間自然乾燥させた後、バイオスキンプレートのL、aおよびbをデジアイ・イメージング・システムによって再度測定して、バイオスキンプレート(ITA2)のITA値を計算した。較正曲線に従って、洗い流し/摩耗性試験後の表面密度(SD2)を得た。
ダウコーニングによるダウコーニング(商標)MQ−1640フレーク樹脂、ダウコーニング(商標)MQ−1600固形樹脂、ダウコーニング(商標)670液、ルーブリゾールからのアバルア(商標)UR450、イノレックスからのレキソレッツ(商標)100を含む5種類の膜形成ポリマーの接触角を測定した。ダウコーニング(商標)MQ−1600固形樹脂およびダウコーニング(商標)670液をジメチコン中に、1:9のポリマー対溶媒重量比で分散させた。他の3種類のポリマーをエタノール中に、1:9のポリマー対溶媒重量比で分散させた。
本実施例は、各種の膜形成ポリマーと共に脂肪酸を組成物中へ包含させることで組成物の耐洗い流し性が改善されたことを説明する。
[実施例2]
本実施例は、膜形成ポリマーと共に各種脂肪酸を組成物中に包含することで組成物の耐洗い流し性が改善されたことを説明する。
Claims (12)
- a)化粧品組成物の重量の0.01から9%の、少なくとも85°の接触角を有する膜形成ポリマー(ここで、使用される「接触角」(CA)は、水/蒸気界面が25℃の温度にて固体表面に接する角度を意味する)と、
b)化粧品組成物の重量の0.01から3.5%の脂肪化合物と、
c)化粧品組成物の重量の0.001から7%の光学粒子と
を含み、
前記脂肪化合物が脂肪酸、石鹸およびその混合物より選択され、
前記膜形成ポリマーがシリコーン樹脂であり、該シリコーン樹脂がMQシリコーン樹脂およびTシリコーン樹脂の混合物である、化粧品組成物。 - 前記シリコーン樹脂がトリメチルシロキシシリケートおよびポリプロピルシルセスキオキサンの混合物である、請求項1に記載の化粧品組成物。
- 膜形成ポリマーの量が前記化粧品組成物の0.3から7重量%である、請求項1または2に記載の化粧品組成物。
- 前記脂肪酸がC12−C24脂肪酸である、請求項1から3のいずれか一項に記載の化粧品組成物。
- 前記脂肪酸がステアリン酸、ラウリン酸、パルミチン酸、イソステアリン酸、ミリスチン酸またはその混合物を含む、請求項4に記載の化粧品組成物。
- 前記石鹸がC12−C24脂肪酸の塩である、請求項1から5のいずれか一項に記載の化粧品組成物。
- 膜形成ポリマーの前記脂肪化合物に対する重量比が10:1から1:2である、請求項1から6のいずれか一項に記載の化粧品組成物。
- 前記光学粒子がチタンジオキシド、亜鉛オキシド、ジルコニウムオキシド、マイカ、鉄オキシドまたはその組合せを含む、請求項1から7のいずれか一項に記載の化粧品組成物。
- 前記化粧品組成物の重量の少なくとも20%の水を含む、請求項1から8のいずれか一項に記載の化粧品組成物。
- 前記化粧品組成物の重量の少なくとも40%の水を含む、請求項9に記載の化粧品組成物。
- 皮膚に請求項1から10のいずれか一項に記載の化粧品組成物を局所適用するステップを含む、皮膚特性を改善する方法。
- 不透明性、不透明性の持続性、光学粒子の累積被着、耐洗い流し性、耐摩耗性またはその組合せより選択されるいずれかの属性を改善するための、請求項1から10のいずれか一項に記載の化粧品組成物の使用。
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CNPCT/CN2012/087301 | 2012-12-24 | ||
CN2012087267 | 2012-12-24 | ||
CNPCT/CN2012/087267 | 2012-12-24 | ||
CN2012087301 | 2012-12-24 | ||
EP13153664.1 | 2013-02-01 | ||
EP13153662 | 2013-02-01 | ||
EP13153662.5 | 2013-02-01 | ||
EP13153664 | 2013-02-01 | ||
PCT/CN2013/089863 WO2014101701A1 (en) | 2012-12-24 | 2013-12-18 | Cosmetic composition |
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