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JP3565332B2 - Emulsion type solid cosmetic - Google Patents
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JP3565332B2 - Emulsion type solid cosmetic - Google Patents

Emulsion type solid cosmetic Download PDF

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Publication number
JP3565332B2
JP3565332B2 JP2000296372A JP2000296372A JP3565332B2 JP 3565332 B2 JP3565332 B2 JP 3565332B2 JP 2000296372 A JP2000296372 A JP 2000296372A JP 2000296372 A JP2000296372 A JP 2000296372A JP 3565332 B2 JP3565332 B2 JP 3565332B2
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Japan
Prior art keywords
sucrose
fatty acid
carbon atoms
monoester
glyceryl
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Expired - Fee Related
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JP2000296372A
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Japanese (ja)
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JP2002104927A (en
Inventor
尚美 辰巳
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Noevir Co Ltd
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Noevir Co Ltd
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Priority to JP2000296372A priority Critical patent/JP3565332B2/en
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Description

【0001】
【発明の属する技術分野】
本発明は、低温下における硬度上昇や経時的な硬度上昇が改善されて製剤安定性に優れ、しかも皮膚に対し低刺激性である乳化型固形化粧料に関する。さらに詳しくは、(A)ショ糖と炭素数が16以上の直鎖飽和脂肪酸とのモノエステル、(B)炭素数が16以上の直鎖飽和脂肪酸のグリセリルモノエステル、及び常温で固形状を呈する油性物質を含有する乳化化粧料において、(C)ショ糖と炭素数が14以下の脂肪酸とのモノエステル及び(D)炭素数が14以下の脂肪酸のポリグリセリルモノエステルより成る群から選択される1種又は2種以上を、さらに含有して成る乳化型固形化粧料に関する。
【0002】
【従来の技術】
エモリエントクリーム,マッサージクリーム,クレンジングクリーム,メイクアップクリーム等に代表される乳化型固形化粧料においては、化粧料の硬度を保持するため、常温で固形状を呈する油脂類やロウ類などが汎用される。また、皮膚に対し低刺激性であることや、生分解性が良好であることなどから、ショ糖の脂肪酸エステルやグリセリン等多価アルコールの脂肪酸エステルといった非イオン性界面活性剤の使用が検討されてきた。酸化安定性を維持し、化粧料の形状を固形状に保つ上で、これらを構成する脂肪酸については、炭素数が16以上の直鎖状で飽和のものが主に使用されてきた。
【0003】
しかしながら、ショ糖と炭素数が16以上の直鎖飽和脂肪酸とのモノエステル、及び炭素数が16以上の直鎖飽和脂肪酸のグリセリルモノエステルを用い、さらに常温で固形状を呈する油脂類やロウ類等を含有させて成る乳化型の固形化粧料においては、低温下において硬度が上昇し、また経時的にも硬度の上昇が見られ、製剤安定性の上で大きな問題となっていた。
【0004】
【発明が解決しようとする課題】
そこで本発明においては、ショ糖と炭素数が16以上の直鎖飽和脂肪酸とのモノエステル、炭素数が16以上の直鎖飽和脂肪酸のグリセリルモノエステル、及び常温で固形状を呈する油性物質を含有して成る乳化型固形化粧料における、上記したような低温下又は経時における硬度上昇を抑制し、製剤安定性が良好で、しかも皮膚に対し低刺激性である乳化型の固形化粧料を得ることを目的とした。
【0005】
【課題を解決するための手段】
上記課題を解決するため種々検討した結果、(A)ショ糖と炭素数が16以上の直鎖飽和脂肪酸とのモノエステル、(B)炭素数が16以上の直鎖飽和脂肪酸のグリセリルモノエステル、及び常温で固形状を呈する油性物質を含有する乳化化粧料に、(C)ショ糖と炭素数が14以下の脂肪酸とのモノエステル及び(D)炭素数が14以下の脂肪酸のポリグリセリルモノエステルより成る群から選択される1種又は2種以上をさらに含有させることにより、低温下における硬度上昇及び経時的な硬度上昇を有効に抑制することができ、しかも皮膚に対する刺激性も低いことを見いだし、本発明を完成するに至った。
【0006】
【発明の実施の形態】
本発明において、(A)成分として用いるショ糖と炭素数が16以上の直鎖飽和脂肪酸とのモノエステルとしては、ショ糖モノパルミチン酸エステル,ショ糖モノマルガリン酸エステル,ショ糖モノステアリン酸エステル,ショ糖モノアラキン酸エステル,ショ糖モノベヘン酸エステル,ショ糖モノリグノセリン酸エステル等が挙げられ、これらの中でも、炭素数が16〜22のものが好ましく用いられる。
【0007】
また、(B)成分として用いる炭素数が16以上の直鎖飽和脂肪酸のグリセリルモノエステルとしては、モノパルミチン酸グリセリル,モノマルガリン酸グリセリル,モノステアリン酸グリセリル,モノアラキン酸グリセリル,モノベヘン酸グリセリル,モノリグノセリン酸グリセリル等が挙げられ、これらの中でも、炭素数が16〜22のものが好ましく用いられる。
【0008】
本発明において用いる常温で固形状を呈する油性物質としては、モクロウ,牛脂,硬化牛脂,硬化大豆油,硬化ヒマシ油等の固形状油脂類、カルナウバロウ,キャンデリラロウ,水添ホホバ油等の植物ロウ類、ミツロウ,鯨ロウ,ラノリン,還元ラノリン,硬質ラノリン等の動物ロウ類、オゾケライト,セレシン,マイクロクリスタリンワックス等の固形状炭化水素類、トリ牛脂脂肪酸グリセリル,トリステアリン酸グリセリル,トリパルミチン酸グリセリル,トリベヘン酸グリセリル,トリミリスチン酸グリセリル,トリヤシ油脂肪酸グリセリル,トリラウリン酸グリセリル,トリラノリン脂肪酸グリセリル等の固形状脂肪酸トリグリセリドなどが挙げられる。
【0009】
次に、本発明において上記した(A),(B)成分及び常温で固形状を呈する油性物質と併用する(C)のショ糖と炭素数が14以下の脂肪酸とのモノエステルとしては、ショ糖モノカプリン酸エステル,ショ糖モノウンデカン酸エステル,ショ糖モノラウリン酸エステル,ショ糖モノトリデカン酸エステル,ショ糖モノミリスチン酸エステル,ショ糖モノカプロレイン酸エステル,ショ糖モノ9−ウンデシレン酸エステル,ショ糖モノ10−ウンデシレン酸エステル,ショ糖モノ2−ラウロレイン酸エステル,ショ糖モノリンデル酸エステル,ショ糖モノトウハク酸エステル,ショ糖モノ5−ラウロレイン酸エステル,ショ糖モノ11−ラウロレイン酸エステル,ショ糖モノ2−トリデセン酸エステル,ショ糖モノcis−9−トリデセン酸エステル,ショ糖モノ12−トリデセン酸エステル,ショ糖モノツズ酸エステル,ショ糖モノ5−ミリストレイン酸エステル,ショ糖モノ9−ミリストレイン酸エステル等が挙げられる。これらの中でも、HLB値が12以上のものが好ましく、また脂肪酸の炭素数が12〜14のものが好ましい。
【0010】
また、本発明において上記(A),(B)成分及び常温で固形状を呈する油性物質と併用する(D)の炭素数が14以下の脂肪酸のポリグリセリルモノエステルとしては、モノカプリン酸ヘキサグリセリル,モノウンデカン酸ヘキサグリセリル,モノラウリン酸ヘキサグリセリル,モノトリデカン酸ヘキサグリセリル,モノミリスチン酸ヘキサグリセリル,モノカプロレイン酸ヘキサグリセリル,モノ9−ウンデシレン酸ヘキサグリセリル,モノ10−ウンデシレン酸ヘキサグリセリル,モノ2−ラウロレイン酸ヘキサグリセリル,モノリンデル酸ヘキサグリセリル,モノトウハク酸ヘキサグリセリル,モノ5−ラウロレイン酸ヘキサグリセリル,モノ11−ラウロレイン酸ヘキサグリセリル,モノ2−トリデセン酸ヘキサグリセリル,モノcis−9−トリデセン酸ヘキサグリセリル,モノ12−トリデセン酸ヘキサグリセリル,モノツズ酸ヘキサグリセリル,モノ5−ミリストレイン酸ヘキサグリセリル,モノ9−ミリストレイン酸ヘキサグリセリル,モノカプリン酸デカグリセリル,モノウンデカン酸デカグリセリル,モノラウリン酸デカグリセリル,モノトリデカン酸デカグリセリル,モノミリスチン酸デカグリセリル,モノカプロレイン酸デカグリセリル,モノ9−ウンデシレン酸デカグリセリル,モノ10−ウンデシレン酸デカグリセリル,モノ2−ラウロレイン酸デカグリセリル,モノリンデル酸デカグリセリル,モノトウハク酸デカグリセリル,モノ5−ラウロレイン酸デカグリセリル,モノ11−ラウロレイン酸デカグリセリル,モノ2−トリデセン酸デカグリセリル,モノcis−9−トリデセン酸デカグリセリル,モノ12−トリデセン酸デカグリセリル,モノツズ酸デカグリセリル,モノ5−ミリストレイン酸デカグリセリル,モノ9−ミリストレイン酸デカグリセリル等が挙げられる。これらの中でも、HLB値が12以上のものが好ましく、また脂肪酸の炭素数が12〜14のものが好ましい。
【0011】
本発明においては、上記(C)及び(D)より成る群から1種又は2種以上を選択し、(A),(B)成分及び常温で固形状を呈する油性物質と併用して用いる。本発明に係る乳化型固形化粧料においては、(A)成分と(C)成分を合わせて1.0〜10.0重量%、(B)成分を1.0〜5.0重量%、常温で固形状を呈する油性物質を1.0〜10.0重量%(さらに好ましくは3.0〜8.0重量%)、(D)成分を0.1〜5.0重量%含有させることが好ましい。また、(A)と(C)との重量比及び(A)と(D)との重量比を、それぞれ8:1〜1:1とすることが好ましい。
【0012】
本発明に係る乳化型固形化粧料は、エモリエントクリーム,マッサージクリーム等の皮膚用化粧料、クレンジングクリーム等の洗浄用化粧料、メイクアップクリーム,ベースクリーム等の下地化粧料、サンスクリーンクリーム,サンタンクリーム等の日焼け止めもしくは日焼け用化粧料、ヘアクリーム等の毛髪用化粧料、ハンドクリーム,ネッククリーム,レッグクリーム等の身体用化粧料などとして提供され得る。
【0013】
さらに本発明に係る乳化型固形化粧料においては、上記(A)〜(D)の各成分及び常温で固形状を呈する油性物質の他に、本発明の特徴を損なわない範囲で、油脂,炭化水素油,エステル油,高級アルコール等の他の油性成分、他の界面活性剤、多価アルコール,アミノ酸等の保湿剤、水溶性高分子化合物、防菌防黴剤、抗酸化剤、塩基成分等、一般的な化粧料用成分を含有させることができる。
【0014】
【実施例】
さらに本発明の特徴について、実施例により詳細に説明する。
【0015】
[実施例1〜実施例7] マッサージクリーム
以下に示す処方により、本発明に係るマッサージクリームとして、実施例1〜実施例7を調製した。また、同時に比較例1〜比較例3を調製した。
(1)ミツロウ 6.00(重量%)
(2)スクワラン 33.00
(3)オクタン酸セチル 16.00
(4)ベヘニルアルコール 1.00
(5)表1に示す(B)成分 表1に示す量
(6)表1に示す(A)成分 表1に示す量
(7)表1に示す(C)成分 表1に示す量
(8)表1に示す(D)成分 表1に示す量
(9)N−ステアロイル−L−グルタミン酸ナトリウム 0.30
(10)1,3−ブチレングリコール 6.00
(11)カルボキシビニルポリマー 0.20
(12)パラオキシ安息香酸メチル 0.05
(13)L−アルギニン 0.25
(14)精製水 全量を100.00とする量
製法:(1)〜(5)の油相成分を混合して加熱溶解し、75℃とする。(13)を(14)の一部に溶解して水溶液とする。(6)〜(12)を(14)の残部に添加溶解して、75℃に加熱し、これに前記油相成分を添加,混合してホモジナイザーにより均一に乳化し、(13)の水溶液を添加,混合した後、冷却する。
【0016】
【表1】

Figure 0003565332
【0017】
上記実施例1〜実施例7及び比較例1〜比較例3について、低温下における硬度変化と経時的な硬度変化を観察した。まず、実施例及び比較例のそれぞれを25℃及び5℃の各温度にて24時間静置した後、不動工業株式会社製レオメーターにて硬度を測定し、次いで25℃で3カ月間静置した後の硬度を同様に測定して、それぞれの測定値を比較した。結果は表2に示す。
【0018】
【表2】
Figure 0003565332
【0019】
低温時における硬度変化としては、5℃にて24時間静置後の硬度が500を超えると使用性が低下する。また、硬度の経時変化としては、25℃にて3カ月間静置後の硬度が200を超えると、使用上問題となる。表2より明らかなように、本発明の実施例1〜実施例7については、5℃,24時間静置後の硬度が172〜450であり、25℃,3カ月間静置後の硬度についても51〜98と、硬度の上昇は使用上問題のない範囲内に抑制されていた。これに対し、比較例1〜比較例3はすべて25℃,3カ月間静置後の硬度が200を超えており、比較例1及び比較例2については、5℃,24時間静置後の硬度上昇も顕著に認められていた。
【0020】
続いて、本発明に係る他の実施例の処方を示す。
【0021】
[実施例8] エモリエントクリーム
(1)ミツロウ 6.0(重量%)
(2)スクワラン 25.0
(3)ホホバ油 5.0
(4)ミリスチン酸イソセチル 15.0
(5)モノステアリン酸グリセリル 2.0
(6)ショ糖モノステアリン酸エステル 4.0
(7)ショ糖モノラウリン酸エステル 1.5
(8)モノラウリン酸デカグリセリル 0.5
(9)1,3−ブチレングリコール 6.0
(10)グリセリン 4.0
(11)パラオキシ安息香酸メチル 0.1
(12)精製水 30.7
(13)ヒアルロン酸ナトリウム1.0重量%水溶液 0.1
(14)香料 0.1
製法:(1)〜(5)の油相成分を混合,加熱溶解して、75℃とする。一方、(6)〜(12)の水相成分を混合,溶解して75℃とし、これに前記油相成分を加えて混合し、ホモジナイザーにて均一に乳化する。次いで冷却し、40℃にて(13),(14)を添加,混合する。
【0022】
[実施例9] クレンジングクリーム
(1)カルナウバロウ 5.0(重量%)
(2)ワセリン 10.0
(3)流動パラフィン 38.0
(4)ミリスチン酸イソプロピル 10.0
(5)モノステアリン酸グリセリル 2.5
(6)ポリオキシエチレン(20E.O.)ソルビタン 0.5
モノステアリン酸エステル
(7)ショ糖モノパルミチン酸エステル 5.0
(8)モノラウリン酸ヘキサグリセリル 1.5
(9)モノミリスチン酸デカグリセリル 1.5
(10)プロピレングリコール 5.0
(11)パラオキシ安息香酸メチル 0.1
(12)精製水 20.8
(13)香料 0.1
製法:(1)〜(6)の油相成分を混合,加熱溶解して、75℃とする。一方、(7)〜(12)の水相成分を混合,溶解して75℃とし、これに前記油相成分を加えて混合し、ホモジナイザーにて均一に乳化する。次いで冷却し、40℃にて(13)を添加,混合する。
【0023】
[実施例10] メイクアップクリーム
(1)マイクロクリスタリンワックス 2.5(重量%)
(2)セタノール 2.0
(3)グリセリルトリ2−エチルヘキサン酸エステル 10.0
(4)モノパルミチン酸グリセリル 2.0
(5)ショ糖モノステアリン酸エステル 5.5
(6)ショ糖モノラウリン酸エステル 1.0
(7)ショ糖モノミリスチン酸エステル 0.2
(8)1,3−ブチレングリコール 10.0
(9)パラオキシ安息香酸メチル 0.1
(10)精製水 64.1
(11)酸化チタン 2.0
(12)ベンガラ 0.4
(13)黄酸化鉄 0.1
(14)香料 0.1
製法:(1)〜(4)の油相成分を混合,加熱溶解して、75℃とする。一方、(5)〜(10)の水相成分を混合,加熱溶解し、(11)〜(13)の顔料成分を添加してホモミキサーにて均一に分散して75℃とする。次いでこの水相成分に前記油相成分を加えて混合し、ホモジナイザーにて均一に乳化する。次いで冷却し、40℃にて(14)を添加,混合する。
【0024】
本発明の実施例1〜実施例10について使用試験を行い、5℃にて1日保存した後の使用性、室温にて1年間保存した後の指へのとれと伸び、及び皮膚刺激感について評価した。その際、実施例8〜実施例10において、それぞれ含有されるショ糖モノラウリン酸エステル,ショ糖モノミリスチン酸エステル,モノラウリン酸ヘキサグリセリル,モノラウリン酸デカグリセリル及びモノミリスチン酸デカグリセリルを、すべて精製水に代替したものを比較例4〜比較例6とし、比較例1〜比較例3とともに同時に使用試験に供した。
【0025】
使用試験は、20才代〜50才代の女性パネラー20名を1群とし、各群に実施例及び比較例のそれぞれをブラインドにて使用させて行った。5℃にて1日保存した後の使用性については、各試料を指にとって皮膚上に塗布した際に使用に耐え得るかどうかを評価させ、「充分使用に耐え得る;3点」,「やや使用しにくい;2点」,「使用に耐えない;1点」として点数化させて20名の平均値を算出した。室温にて1年間保存した後の指へのとれと伸び、及び皮膚刺激感については、表3に示す基準に従って官能評価させて点数化し、20名の平均値を算出して表4に示した。
【0026】
【表3】
Figure 0003565332
【0027】
【表4】
Figure 0003565332
【0028】
表4より明らかなように、本発明の実施例については、5℃で保存した後においても、ほぼ使用に耐え得ると評価されていた。一方、比較例3以外の比較例については、5℃程度の低温下に置かれた場合に、使用性が著しく損なわれることが示されていた。また室温保存後の指へのとれ及び伸びについて、実施例使用群では全群でほぼ良好な評価が得られていた。これに対し比較例使用群では、全群において評価は低くなっていた。また、本発明の実施例使用群及び比較例使用群においては、使用時に問題となる皮膚の刺激感は認められていなかった。
【0029】
さらに本発明の実施例1〜実施例10については、男性パネラー30名を1群とする48時間の背部閉塞貼付試験においても、皮膚刺激性反応は認められなかった。
【0030】
【発明の効果】
以上詳述したように、本発明により、ショ糖と炭素数が16以上の直鎖飽和脂肪酸とのモノエステル、炭素数が16以上の直鎖飽和脂肪酸のグリセリルモノエステル、及び常温で固形状を呈する油性物質を含有して成る乳化型固形化粧料における、低温下における硬度上昇や経時的な硬度上昇が改善され、製剤安定性に優れ、しかも皮膚に対し低刺激性である乳化型固形化粧料を得ることができた。[0001]
TECHNICAL FIELD OF THE INVENTION
TECHNICAL FIELD The present invention relates to an emulsified solid cosmetic which has improved formulation stability at low temperatures and improved hardness over time, has excellent formulation stability, and has low skin irritation. More specifically, (A) a monoester of sucrose and a straight-chain saturated fatty acid having 16 or more carbon atoms, (B) a glyceryl monoester of a straight-chain saturated fatty acid having 16 or more carbon atoms, and a solid at room temperature. In an emulsified cosmetic containing an oily substance, 1 is selected from the group consisting of (C) a monoester of sucrose and a fatty acid having 14 or less carbon atoms and (D) a polyglyceryl monoester of a fatty acid having 14 or less carbon atoms. The present invention relates to an emulsified solid cosmetic further comprising one or more kinds.
[0002]
[Prior art]
In emulsifying solid cosmetics represented by emollient creams, massage creams, cleansing creams, make-up creams, etc., oils and waxes that are solid at room temperature are commonly used in order to maintain the hardness of the cosmetics. . In addition, the use of nonionic surfactants such as fatty acid esters of sucrose and fatty acid esters of polyhydric alcohols such as glycerin has been studied because of their low irritation to the skin and good biodegradability. Have been. In order to maintain oxidative stability and maintain the shape of cosmetics in a solid state, fatty acids constituting these are mainly linear and saturated fatty acids having 16 or more carbon atoms.
[0003]
However, a monoester of sucrose and a linear saturated fatty acid having 16 or more carbon atoms and a glyceryl monoester of a linear saturated fatty acid having 16 or more carbon atoms are used, and further, fats and oils and waxes exhibiting a solid state at normal temperature. In the case of emulsified solid cosmetics containing such an ingredient, the hardness increases at a low temperature, and the hardness also increases over time, which has been a major problem in the stability of preparations.
[0004]
[Problems to be solved by the invention]
Therefore, in the present invention, a monoester of sucrose and a straight-chain saturated fatty acid having 16 or more carbon atoms, a glyceryl monoester of a straight-chain saturated fatty acid having 16 or more carbon atoms, and an oily substance which exhibits a solid state at normal temperature are contained. To obtain an emulsified solid cosmetic composition comprising the above-mentioned emulsified solid cosmetic composition, which suppresses an increase in hardness at a low temperature or over time as described above, has good formulation stability, and has low skin irritation. Aimed at.
[0005]
[Means for Solving the Problems]
As a result of various studies to solve the above problems, (A) a monoester of sucrose and a linear saturated fatty acid having 16 or more carbon atoms, (B) a glyceryl monoester of a linear saturated fatty acid having 16 or more carbon atoms, And (C) a monoester of sucrose and a fatty acid having a carbon number of 14 or less and (D) a polyglyceryl monoester of a fatty acid having a carbon number of 14 or less. By further containing one or more selected from the group consisting of, it is possible to effectively suppress the increase in hardness at low temperatures and the increase in hardness over time, and also find that the skin has low irritation, The present invention has been completed.
[0006]
BEST MODE FOR CARRYING OUT THE INVENTION
In the present invention, the monoester of sucrose and a linear saturated fatty acid having 16 or more carbon atoms used as the component (A) includes sucrose monopalmitate, sucrose monomalgalate, sucrose monostearate, Examples thereof include sucrose monoarachinate, sucrose monobehenate, and sucrose monolignocerate, among which those having 16 to 22 carbon atoms are preferably used.
[0007]
The glyceryl monoester of a linear saturated fatty acid having 16 or more carbon atoms used as the component (B) includes glyceryl monopalmitate, glyceryl monomalgallate, glyceryl monostearate, glyceryl monoarachiate, glyceryl monobehenate, and monolignoserine. And glyceryl acid. Among them, those having 16 to 22 carbon atoms are preferably used.
[0008]
Examples of the oily substance which exhibits a solid state at normal temperature used in the present invention include solid oils and fats such as mokuro, tallow, hardened tallow, hardened soybean oil, hardened castor oil and the like, and vegetable waxes such as carnauba wax, candelilla wax and hydrogenated jojoba oil. , Animal waxes such as beeswax, whale wax, lanolin, reduced lanolin, hard lanolin, solid hydrocarbons such as ozokerite, ceresin, microcrystalline wax, triglyceride triglyceride, glyceryl tristearate, glyceryl tripalmitate, Examples include solid fatty acid triglycerides such as glyceryl tribehenate, glyceryl trimyristate, glyceryl tricoconut oil, glyceryl trilaurate, and glyceryl trilanolin fatty acid.
[0009]
Next, in the present invention, as the monoester of sucrose and a fatty acid having 14 or less carbon atoms, which is used in combination with the above-mentioned components (A) and (B) and the oily substance which exhibits a solid state at normal temperature, is sucrose. Sugar monocaprate, sucrose monoundecanoate, sucrose monolaurate, sucrose monotridecanoate, sucrose monomyristate, sucrose monocaprolate, sucrose mono9-undecylate, sucrose Sugar mono 10-undecylenate, sucrose mono 2-laurate, sucrose monolindelate, sucrose monosuccinate, sucrose mono 5-laurate, sucrose mono 11-laurate, sucrose Mono 2-tridecene ester, sucrose mono cis-9-tridecene Ester, sucrose mono-12-tridecenoic acid esters, sucrose Monotsuzu acid ester, sucrose mono-5-myristoleic acid ester, sucrose mono-9-myristoleic acid esters. Among them, those having an HLB value of 12 or more are preferable, and those having a fatty acid having 12 to 14 carbon atoms are preferable.
[0010]
In the present invention, the polyglyceryl monoester of a fatty acid having 14 or less carbon atoms of (D) used in combination with the components (A) and (B) and an oily substance which exhibits a solid state at normal temperature includes hexaglyceryl monocaprate, Hexaglyceryl monoundecanoate, Hexaglyceryl monolaurate, Hexaglyceryl monotridecanoate, Hexaglyceryl monomyristate, Hexaglyceryl monocaprolate, Hexaglyceryl mono9-undecylenate, Hexaglyceryl mono10-undecylenate, Mono-2-lauroleic acid Hexaglyceryl, hexaglyceryl monolindelate, hexaglyceryl monosuccinate, hexaglyceryl mono-5-laurate, hexaglyceryl mono-11-lauroate, hexaglyceryl mono-2-tridecenoate, mono Hexaglyceryl is-9-tridecenoate, hexaglyceryl mono-12-tridecenoate, hexaglyceryl monotuzunate, hexaglyceryl mono-5-myristoleate, hexaglyceryl mono9-myristoleate, decaglyceryl monocaprate, deca monoundecanoate Glyceryl, decaglyceryl monolaurate, decaglyceryl monotridecanoate, decaglyceryl monomyristate, decaglyceryl monocaproleate, decaglyceryl mono9-undecylenate, decaglyceryl mono10-undecylenate, decaglyceryl mono-2-laurolate, mono Decaglyceryl lindelate, decaglyceryl monosuccinate, decaglyceryl mono-5-laurate, decaglyceryl mono-11-lauroate, decaglycerate mono-2-tridecenoate Lil, mono cis-9-tridecenoic decaglyceryl mono- 12-tridecenoic decaglyceryl, Monotsuzu decaglyceryl mono- 5- myristoleic decaglyceryl mono- 9-myristoleic decaglyceryl the like. Among them, those having an HLB value of 12 or more are preferable, and those having a fatty acid having 12 to 14 carbon atoms are preferable.
[0011]
In the present invention, one or more kinds are selected from the group consisting of the above (C) and (D), and used in combination with the components (A) and (B) and the oily substance which is solid at room temperature. In the emulsified solid cosmetic according to the present invention, the components (A) and (C) are combined at 1.0 to 10.0% by weight, and the component (B) is 1.0 to 5.0% by weight at room temperature. 1.0 to 10.0% by weight (more preferably 3.0 to 8.0% by weight) of a solid oily substance, and 0.1 to 5.0% by weight of the component (D). preferable. The weight ratio of (A) to (C) and the weight ratio of (A) to (D) are preferably set to 8: 1 to 1: 1.
[0012]
Emulsifying solid cosmetics according to the present invention include skin cosmetics such as emollient creams and massage creams, cleaning cosmetics such as cleansing creams, base cosmetics such as makeup creams and base creams, sunscreen creams and suntan creams. And sunscreen cosmetics, hair cosmetics such as hair creams, and body cosmetics such as hand creams, neck creams, and leg creams.
[0013]
Further, in the emulsified solid cosmetic according to the present invention, in addition to the components (A) to (D) and the oily substance which exhibits a solid state at ordinary temperature, oils and fats, carbonized oils and the like may be used as long as the characteristics of the present invention are not impaired. Other oily components such as hydrogen oil, ester oil, higher alcohol, other surfactants, humectants such as polyhydric alcohols and amino acids, water-soluble polymer compounds, antibacterial and fungicides, antioxidants, base components, etc. General cosmetic ingredients can be contained.
[0014]
【Example】
Further, features of the present invention will be described in detail with reference to examples.
[0015]
[Examples 1 to 7] Massage creams Examples 1 to 7 were prepared as massage creams according to the present invention by the following formulation. Simultaneously, Comparative Examples 1 to 3 were prepared.
(1) Beeswax 6.00 (% by weight)
(2) Squalane 33.00
(3) Cetyl octoate 16.00
(4) Behenyl alcohol 1.00
(5) Component shown in Table 1 Component (B) Amount shown in Table 1 (6) Component shown in Table 1 (A) Component shown in Table 1 (7) Component shown in Table 1 (C) Component shown in Table 1 (8 ) (D) component shown in Table 1) Amount shown in Table 1 (9) N-stearoyl-L-sodium glutamate 0.30
(10) 1,3-butylene glycol 6.00
(11) Carboxyvinyl polymer 0.20
(12) Methyl paraoxybenzoate 0.05
(13) L-arginine 0.25
(14) Purified water Amount to make the total amount 100.00 Production method: The oil phase components (1) to (5) are mixed, heated and dissolved, and brought to 75 ° C. (13) is dissolved in a part of (14) to form an aqueous solution. (6) to (12) are added and dissolved in the remainder of (14), heated to 75 ° C., the oil phase component is added thereto, mixed, and uniformly emulsified by a homogenizer, and the aqueous solution of (13) is added. After addition and mixing, the mixture is cooled.
[0016]
[Table 1]
Figure 0003565332
[0017]
With respect to Examples 1 to 7 and Comparative Examples 1 to 3, a change in hardness at a low temperature and a change in hardness over time were observed. First, each of the Examples and Comparative Examples was allowed to stand at 25 ° C. and 5 ° C. for 24 hours, and then measured for hardness with a rheometer manufactured by Fudo Kogyo Co., Ltd., and then allowed to stand at 25 ° C. for 3 months. After that, the hardness was similarly measured, and the respective measured values were compared. The results are shown in Table 2.
[0018]
[Table 2]
Figure 0003565332
[0019]
As for a change in hardness at a low temperature, if the hardness after standing at 5 ° C. for 24 hours exceeds 500, the usability decreases. Regarding the change with time in hardness, if the hardness after standing at 25 ° C. for 3 months exceeds 200, there is a problem in use. As is clear from Table 2, in Examples 1 to 7 of the present invention, the hardness after standing at 5 ° C. for 24 hours is 172 to 450, and the hardness after standing at 25 ° C. for 3 months. The hardness was 51 to 98, and the increase in hardness was suppressed within a range where there was no problem in use. In contrast, Comparative Examples 1 to 3 all had a hardness of more than 200 after standing at 25 ° C. for 3 months, and Comparative Examples 1 and 2 had a hardness after standing at 5 ° C. for 24 hours. A remarkable increase in hardness was also observed.
[0020]
Subsequently, the prescription of another example according to the present invention will be described.
[0021]
Example 8 Emollient Cream (1) Beeswax 6.0 (% by weight)
(2) Squalane 25.0
(3) Jojoba oil 5.0
(4) Isocetyl myristate 15.0
(5) Glyceryl monostearate 2.0
(6) Sucrose monostearate 4.0
(7) Sucrose monolaurate 1.5
(8) Decaglyceryl monolaurate 0.5
(9) 1,3-butylene glycol 6.0
(10) Glycerin 4.0
(11) Methyl paraoxybenzoate 0.1
(12) Purified water 30.7
(13) 1.0% by weight aqueous solution of sodium hyaluronate 0.1
(14) Fragrance 0.1
Production method: The oil phase components (1) to (5) are mixed and dissolved by heating to 75 ° C. On the other hand, the aqueous phase components (6) to (12) are mixed and dissolved to 75 ° C., and the oil phase component is added thereto, mixed, and uniformly emulsified by a homogenizer. Then, the mixture is cooled, (13) and (14) are added and mixed at 40 ° C.
[0022]
[Example 9] Cleansing cream (1) Carnauba wax 5.0 (% by weight)
(2) Vaseline 10.0
(3) Liquid paraffin 38.0
(4) Isopropyl myristate 10.0
(5) Glyceryl monostearate 2.5
(6) Polyoxyethylene (20EO) sorbitan 0.5
Monostearate (7) Sucrose monopalmitate 5.0
(8) Hexaglyceryl monolaurate 1.5
(9) Decaglyceryl monomyristate 1.5
(10) Propylene glycol 5.0
(11) Methyl paraoxybenzoate 0.1
(12) Purified water 20.8
(13) Fragrance 0.1
Production method: The oil phase components (1) to (6) are mixed and dissolved by heating to 75 ° C. On the other hand, the aqueous phase components (7) to (12) are mixed and dissolved to 75 ° C., and the oil phase component is added thereto, mixed, and uniformly emulsified by a homogenizer. Then, the mixture is cooled and (13) is added and mixed at 40 ° C.
[0023]
[Example 10] Make-up cream (1) Microcrystalline wax 2.5 (% by weight)
(2) Cetanol 2.0
(3) Glyceryl tri-2-ethylhexanoate 10.0
(4) Glyceryl monopalmitate 2.0
(5) Sucrose monostearate 5.5
(6) Sucrose monolaurate 1.0
(7) Sucrose monomyristate 0.2
(8) 1,3-butylene glycol 10.0
(9) Methyl paraoxybenzoate 0.1
(10) Purified water 64.1
(11) Titanium oxide 2.0
(12) Bengala 0.4
(13) Yellow iron oxide 0.1
(14) Fragrance 0.1
Production method: The oil phase components (1) to (4) are mixed and dissolved by heating to 75 ° C. On the other hand, the aqueous phase components of (5) to (10) are mixed and dissolved by heating, and the pigment components of (11) to (13) are added and uniformly dispersed by a homomixer to 75 ° C. Next, the oil phase component is added to the aqueous phase component, mixed, and uniformly emulsified by a homogenizer. Then, the mixture is cooled and (14) is added and mixed at 40 ° C.
[0024]
A usage test was conducted on Examples 1 to 10 of the present invention, and the usability after storage at 5 ° C. for one day, the removal and elongation to the finger after storage at room temperature for one year, and the feeling of skin irritation evaluated. At that time, in Examples 8 to 10, sucrose monolaurate, sucrose monomyristate, hexaglyceryl monolaurate, decaglyceryl monolaurate, and decaglyceryl monomyristate contained in purified water were all contained. The alternatives were referred to as Comparative Examples 4 to 6, and were subjected to use tests simultaneously with Comparative Examples 1 to 3.
[0025]
The use test was conducted by setting 20 female panelists in their 20s to 50s as one group, and using each of the examples and the comparative examples in a blind. With respect to the usability after storage at 5 ° C. for 1 day, each sample was evaluated for whether it was durable when applied to the finger and applied to the skin. Difficult to use; 2 points "and" Not usable; 1 point "were scored and the average value of 20 persons was calculated. After storage at room temperature for one year, the peeling and elongation to the finger and the feeling of skin irritation were scored by sensory evaluation according to the criteria shown in Table 3, and the average value of 20 persons was calculated and shown in Table 4. .
[0026]
[Table 3]
Figure 0003565332
[0027]
[Table 4]
Figure 0003565332
[0028]
As is evident from Table 4, the examples of the present invention were evaluated to be almost usable even after storage at 5 ° C. On the other hand, in Comparative Examples other than Comparative Example 3, it was shown that the usability was significantly impaired when placed at a low temperature of about 5 ° C. In addition, in the group using the examples, almost good evaluation was obtained in the group using the examples with respect to the removal and the elongation to the finger after storage at room temperature. On the other hand, in the group using the comparative example, the evaluation was low in all groups. In addition, in the group using the examples and the group using the comparative examples of the present invention, no irritating skin sensation which is a problem at the time of use was observed.
[0029]
Furthermore, in Examples 1 to 10 of the present invention, no skin irritating reaction was observed in a 48-hour back obstruction sticking test using 30 male panelists as a group.
[0030]
【The invention's effect】
As described above in detail, according to the present invention, a monoester of sucrose and a linear saturated fatty acid having 16 or more carbon atoms, a glyceryl monoester of a linear saturated fatty acid having 16 or more carbon atoms, and a solid at room temperature. Emulsion-type solid cosmetics containing an oily substance exhibiting improved hardness at low temperatures and increased hardness over time, exhibit excellent formulation stability, and have low irritation to the skin. Could be obtained.

Claims (2)

(A)ショ糖と炭素数が16以上の直鎖飽和脂肪酸とのモノエステル、および(B)炭素数が16以上の直鎖飽和脂肪酸のグリセリルモノエステルおよび常温で固形状を呈する油性物質を含有し、さらに(C)ショ糖と炭素数が14以下の脂肪酸とのモノエステルおよび(D)炭素数が14以下の脂肪酸のポリグリセリルモノエステルより成る群から選択される1種又は2種以上を含有し、(A)と(C)との重量比および/または(A)と(D)との重量比を、8:1〜1:1とすることを特徴とする乳化型固形化粧料。 (A) a monoester of sucrose and a linear saturated fatty acid having 16 or more carbon atoms, and (B) a glyceryl monoester of a linear saturated fatty acid having 16 or more carbon atoms and an oily substance which exhibits a solid state at normal temperature. And one or more selected from the group consisting of (C) a monoester of sucrose and a fatty acid having 14 or less carbon atoms and (D) a polyglyceryl monoester of a fatty acid having 14 or less carbon atoms. An emulsified solid cosmetic wherein the weight ratio of (A) and (C) and / or the weight ratio of (A) and (D) is 8: 1 to 1: 1. (A)ショ糖と炭素数が16〜22の直鎖飽和脂肪酸とのモノエステル、および(B)炭素数が16〜22の直鎖飽和脂肪酸のグリセリルモノエステルおよび常温で固形状を呈する油性物質を含有し、さらに(C)ショ糖と炭素数が12〜14の脂肪酸とのモノエステルおよび(D)炭素数が12〜14の脂肪酸のポリグリセリルモノエステルより成る群から選択される1種又は2種以上を含有し、(A)と(C)との重量比および/または(A)と(D)との重量比を、8:1〜1:1とすることを特徴とする乳化型固形化粧料。 (A) a monoester of sucrose and a linear saturated fatty acid having 16 to 22 carbon atoms, and (B) a glyceryl monoester of a linear saturated fatty acid having 16 to 22 carbon atoms and an oily substance which exhibits a solid state at normal temperature One or two selected from the group consisting of (C) a monoester of sucrose and a fatty acid having 12 to 14 carbon atoms and (D) a polyglyceryl monoester of a fatty acid having 12 to 14 carbon atoms. And / or (A) and (D), and / or (A) and (D) in a weight ratio of 8: 1 to 1: 1. Cosmetics.
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JP3532910B2 (en) 2002-03-26 2004-05-31 花王株式会社 Cleansing cosmetics
JP4646673B2 (en) * 2005-03-31 2011-03-09 株式会社ナリス化粧品 Emulsified composition
KR101619085B1 (en) * 2009-09-30 2016-05-11 (주)아모레퍼시픽 Cosmetic composition for massage
CN105769662A (en) * 2016-03-16 2016-07-20 广州丹奇日用化工厂有限公司 Cleansing cream with anti-allergy function and method for preparing cleansing cream

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