JP2022031399A - 透明組成物および透明化粧料 - Google Patents
透明組成物および透明化粧料 Download PDFInfo
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Landscapes
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Abstract
【解決手段】
(a)紫外線吸収剤と、
(b)屈折率が1.5~1.7の油分と、
(c)屈折率が1.3~1.5未満の油分と、
(d)屈折率が1.45~1.55の粉末と、
(e)油分増粘剤と
を含み、(b)屈折率が1.5~1.7の油分および(C)屈折率が1.3~1.5未満の油分の混合油分の屈折率が1.44~1.56であり、(e)油分増粘剤をデキストリン脂肪酸エステル、ショ糖脂肪酸エステル、グリセリル脂肪酸エステル、アミノ酸系ゲル化剤(ただし、リジン誘導体変性シリコーンを除く)脂肪酸もしくはその塩、または有機変性粘土鉱物とする。
【選択図】なし
Description
配合した、透明固形組成物が開示されている。
(b)屈折率が1.5~1.7の油分と、
(c)屈折率が1.3~1.5未満の油分と、
(d)屈折率が1.45~1.55の粉末と
を含み、(b)屈折率が1.5~1.7の油分および(C)屈折率が1.3~1.5未満の油分の混合油分の屈折率が1.44~1.56である。
本発明の透明組成物(以下、単に組成物ともいう)は、
(a)紫外線吸収剤と、
(b)屈折率が1.5~1.7の油分と、
(c)屈折率が1.3~1.5未満の油分と、
(d)屈折率が1.45~1.55の粉末と、を含み、(b)屈折率が1.5~1.7の油分および(C)屈折率が1.3~1.5未満の油分の混合油分の屈折率が1.44~1.56である。
以下、各成分について詳細に説明する。
本発明で用いられる(a)紫外線吸収剤(以下、単に(a)成分ともいう)は、化粧料等の皮膚外用剤に配合し得るものから選択され、特に限定はされないが、油溶性吸収剤であることが好ましい。具体例として、例えば、t-ブチルメトキシジベンゾイルメタン、メトキシケイヒ酸エチルヘキシル(オクチルメトキシシンナメート)、サリチル酸フェニル、サリチル酸オクチル、サリチル酸ホモメンチル(ホモサレート)、サリチル酸エチルヘキシル、オクトクリレン、2-ヒドロキシ4-メトキシベンゾフェノン、ポリシリコン-15、エチルヘキシルトリアゾン、エチルヘキシルトリアゾン、ジエチルアミノヒドロキシベンゾイル安息香酸ヘキシル、ビスエチルヘキシルオキシフェノールメトキシフェニルトリアジン、オキシベンゾン-3、メチレンビスベンゾトリアゾリルテトラメチルブチルフェノール、2,4,6-トリアニリノ-p-(カルボ-2’-エチルヘキシル-1’-オキシ)-1,3,5-トリアジン、{2-[4-(ジエチルアミノ)-2-ヒドロキシベンゾイル]}安息香酸ヘキシルエステル、2,4-ビス-[{4-(2-エチルヘキシルオキシ)-2-ヒドロキシ}-フェニル]-6-(4-メトキシフェニル)-1,3,5-トリアジ
ン、ドロメトリゾールトリシロキサン等を挙げることができる。
紫外線吸収剤は単独で用いてもよいし、2種以上を適宜組み合わせて用いてもよい。
(b)屈折率が1.5~1.7の油分は、25℃における屈折率が1.5~1.7の相対的に高い屈折率を有する油分(以下、単に(b)成分あるいは高屈折率油分ともいう)
である。そのような高屈折率油分として、限定はされないが、例えば水添ポリイソブテン、トリメチルペンタフェニルポリシロキサン、ジフェニルシロキシフェニルトリメチコン、ジフェニルジメチコン、マカデミアナッツ脂肪酸フィトステリル、イソステアリン酸フィトステリルなどが挙げられる。例えば、トリメチルペンタフェニルポリシロキサンとして、東レ・ダウコーニング社のPH-1555HRIC(屈折率1.58)、信越化学工業社製のシリコーンKF56(屈折率約1.5)日本ユニカー製のFZ-3156(屈折率:1.575)、ジフェニルジメチコンとして信越化学工業社製のKF-54(屈折率1.505)、マカデミアナッツ脂肪酸フィトステリルとして日本精化社製のPlandool-MAS(屈折率:1.501)等が市販されており、これらを好適に使用することができる。
高屈折率油分は単独で用いてもよいし、2種以上を適宜組み合わせて用いてもよい。
(c)屈折率が1.3~1.5未満の油分は、25℃における屈折率が1.3~1.5未満の相対的に低い屈折率を有する油分(以下、単に(c)成分あるいは低屈折率油分ともいう)である。そのような低屈折率油分として、限定はされないが、例えば、セバシン酸ジイソプロピル(屈折率約1.43)、トリエチルヘキサノイン(屈折率約1.45)、ミリスチン酸イソプロピル(屈折率約1.43)、水添ポリデセン(屈折率約1.46)、トリ(カプリル酸/カプリン酸)グリセリル(屈折率約1.45)、トリ2-エチルヘキサン酸グリセリル(屈折率約1.44)、2-エチルヘキサン酸セチル(屈折率約1.44)、トリオクタン酸トリメチロールプロパン(屈折率約1.45)、スクワラン(屈折率約1.45)、α-オレフィンオリゴマー(屈折率約1.46)、ジイソステアリン酸グリセリル(屈折率約1.46)、リンゴ酸ジイソステアリル(屈折率約1.46)、トリイソステアリン酸ポリグリセリル(屈折率約1.47)、マカデミアナッツ油(屈折率約1.47)、流動パラフィン(屈折率約1.47)、イソドデカン(屈折率約1.42)、イソヘキサデカン(屈折率約1.43)、軽質イソパラフィン(屈折率約1.43)、ジメチルポリシロキサン(屈折率約1.40)、ポリオキシアルキレン・ポリアルキルシロキサン(アルキレン=エチレン:屈折率約1.42)等が挙げられる。特に、セバシン酸ジイソプロピル、トリエチルヘキサノイン、トリ(カプリル酸/カプリン酸)グリセリル等を好ましく用いることができる。
低屈折率油分は単独で用いてもよいし、2種以上を適宜組み合わせて用いてもよい。
がりを付与することは難しい場合があり、また、80質量%を超えて配合するとベタツキが生じる場合がある。(b)成分と(c)成分の配合量を調整して、これら混合油分の平均屈折率が1.44~1.56の範囲内になるように配合する。
(d)屈折率が1.45~1.55の粉末(以下、単に(d)成分ともいう)は、文献値の屈折率が1.45~1.55である粉末である。屈折率がこの範囲であると、本発明で用いられる油性成分との屈折率差が小さく、それによって基剤の高い透明性が実現できる。そのような粉末としては、限定はされないが、例えば、シリカ、ジメチルシリル化シリカ(約1.46)、ポリメタクリル酸メチル(約1.49)、(HDl/トリメチロールヘキシル ラクトン)クロスポリマー(約1.5)、(IPDI/ポリ(1,4-ブタ
ンジオール)-14)クロスポリマー(約1.49)、ナイロン(約1.53)、セルロース(約1.49)、ポリエチレン(約1.51)、ポリウレタン(約1.50)、無水珪酸(約1.45~1.50)等が挙げられる。また、これらの粉末を常法により疎水化処理等の表面処理をして配合してもよい。
本アエロジル株式会社製)、オクチルシラン処理品であるAEROSIL R805(日
本アエロジル株式会社製)、ヘキサメチルジシラザン処理品であるAEROSIL R8
12、R812S、RX200(日本アエロジル株式会社製)、ジメチルシリコーンオイル処理品であるAEROSIL R202、RY200(日本アエロジル株式会社製)等
を挙げることができる。
市販品としては、例えば、ガンツパールGMX-0810(ガンツ化成社製)、マイクロスフェアー M-330(松本油脂製薬社製)等が挙げられる。
市販品としては、例えば、TPパウダー Uシリーズ(東色ピグメント株式会社)等が挙げられる。
<(e)油分増粘剤>
本発明の透明組成物は(e)油分増粘剤を含むことが好ましい。
(e)油分増粘剤(以下、単に(e)成分ともいう)は、化粧料等において油分に溶解または油分で膨潤することにより油分を増粘する効果を発揮する成分として使用されている物質から適宜選択できる。例えば、デキストリン脂肪酸エステル、ショ糖脂肪酸エステル、グリセリル脂肪酸エステル、アミノ酸系ゲル化剤、脂肪酸もしくはその塩、または有機変性粘土鉱物等が好ましい。油分増粘剤は単独で用いてもよいし、2種以上を適宜組み合わせて用いてもよく、2種以上を配合するのが特に好ましい。
ト、ソルビタンモノパルミテート、ソルビタンモノステアレート、ソルビタンセスキオレエート、ソルビタントリオレエート、ペンタ-2-エチルヘキシル酸ジグリセロールソルビタン、テトラ-2-エチルヘキシル酸ジグリセロ-ルソルビタン等);グリセリンポリグリセリン脂肪酸類(例えば、モノ綿実油脂肪酸グリセリン、モノエルカ酸グリセリン、セスキオレイン酸グリセリン、モノステアリン酸グリセリン、α,α’-オレイン酸ピログルタミン酸グリセリン、モノステアリン酸グリセリンリンゴ酸等);プロピレングリコール脂肪酸エステル類(例えば、モノステアリン酸プロピレングリコール等);硬化ヒマシ油誘導体;グリセリンアルキルエーテル等が挙げられる。
ヒマシ油誘導体(例えば、POE-ヒマシ油、POE-硬化ヒマシ油、POE-硬化ヒマシ油モノイソステアレート、POE-硬化ヒマシ油トリイソステアレート、POE-硬化ヒマシ油モノピログルタミン酸モノイソステアリン酸ジエステル、POE-硬化ヒマシ油マレイン酸等);POE-ミツロウ・ラノリン誘導体(例えば、POE-ソルビットミツロウ等);アルカノールアミド(例えば、ヤシ油脂肪酸ジエタノールアミド、ラウリン酸モノエタノールアミド、脂肪酸イソプロパノールアミド等);POE-プロピレングリコール脂肪酸エステル;POE-アルキルアミン;POE-脂肪酸アミド;ショ糖脂肪酸エステル;トリオレイルリン酸等が挙げられる。
れる。
ビタミンとしては、例えば、ビタミンA 、B1、B2、B6、C、Eおよびその誘導
体、パントテン酸およびその誘導体、ビオチン等が挙げられる。
屈折率は、Rudolph Research Analytical社製AUTOMATIC REFRACTOMETERを用いて、25℃で測定した。
[透明性]
光路長10mm×光路幅10mmのプラスティックセルに、実施例および比較例の粉体を含まないベース部分を溶融充填した測定サンプルを、分光光度計(U-4100 HITACHI社製)を用いて700nmの光の波長領域における透過率を測定した。
測定プレート(Sプレート)(5×5cmのV溝PMMA板、SPFMASTER-PA01)に各サンプルを2mg/cm2の量で滴下し、60秒間指で塗布し、15分間乾燥した後に形成された塗膜の吸光度を株式会社日立製作所社製U-4100型自記録分光光度計にて測定した。何も塗布していない測定プレートをコントロールとし、吸光度(Abs)を以下の式で算出した。
Abs=-log(T/To)
T:サンプルの透過率、To:何も塗布していない測定プレートの透過率
測定したプレートを硬度50~500の水に充分に浸し、30分間そのまま水中で静置した。その後、表面の水滴がなくなるまで15~30分程度乾燥させ、再び吸光度を測定し、水浴前後のAbs積算値(波長280~400nmの範囲)からAbs変化率(以下の式)を紫外線防御能向上効果として算出した。
紫外線防御能向上効果:
Abs変化率(%)=(水浴後のAbs積算値)/(水浴前のAbs積算値)×10
0
また、表2に示すように、本発明の透明組成物は油分増粘剤を含む場合(実施例11~15)でも、含まない実施例10と同様に高い透明性、水浴後の紫外線防御効果が向上するという特性を示した。一方、油分増粘剤を含んでいても(d)粉末を含まない比較例2は水浴後の紫外線防御効果が低下した。さらに、表3に示すように、(b)高屈折率油分を含まない比較例3や(c)低屈折率油分を含まない比較例4では、透明性に欠けた。
処方例1:化粧下地
メトキシケイヒ酸エチルヘキシル 5%
ホモサレート 5%
t-ブチルメトキシジベンゾイルメタン 2%
ビスエチルヘキシルオキシフェノールメトキシフェニルトリアジン 1%
ポリアミド-8 20%
エチルヘキサン酸セチル 40%
ジフェニルシロキシフェニルトリメチコン 15%
グリチルレチン酸ステアリル 0.1%
トコフェロール 0.5%
シリカ 5%
ヂプロプレングリコール 1%
トリエチルヘキサノイン 残渣
ヒドロキシステアリン酸 7%
メトキシケイヒ酸エチルヘキシル 10%
サリチル酸エチルヘキシル 5%
ジエチルアミノヒドロキシベンゾイル安息香酸ヘキシル 2%
ビスエチルヘキシルオキシフェノールメトキシフェニルトリアジン 1%
ジブチルラウロイルグルタミド 2%
ポリアミド-8 3%
メタクリル酸メチルクロスポリマー 10%
トリメチルペンタフェニルポリシロキサン 3%
水添ポリデセン 20%
セルロース 0.5%
ジフェニルシロキシフェニルトリメチコン 残渣
ジエチルアミノヒドロキシベンゾイル安息香酸ヘキシル 2%
メトキシケイヒ酸エチルヘキシル 10%
ビスエチルヘキシルオキシフェノールメトキシフェニルトリアジン 1%
トリメチルペンタフェニルポリシロキサン 6%
カプリリルメチコン 20%
ミリスチン酸イソプロピル 5%
イソステアリン酸 0.01%
ジメチルシリル化シリカ 0.5%
ポリアミド-8 10%
ジフェニルシロキシフェニルトリメチコン 残渣
サリチル酸エチルヘキシル 5%
t-ブチルメトキシジベンゾイルメタン 2%
ビスエチルヘキシルオキシフェノールメトキシフェニルトリアジン 1%
オクトクリレン 5%エチルヘキシルトリアゾン 1.5%
ホモサレート 10%
セバシン酸ジイソプロピル 15%
ジピバリン酸PPG-3 15%
セスキイソステアリン酸ソルビタン 0.01%
パルミチン酸デキストリン 2%
(IPDI/ポリ(1,4-ブタンジオール)-14)クロスポリマー 1%
ジブチルラウロイルグルタミド 2%
ジブチルエチルヘキサノイルグルタミド 2%
PEG/PPG-14/7ジメチルエーテル 0.5%
ジフェニルシロキシフェニルトリメチコン 残渣
ホモサレート 5%
サリチル酸エチルヘキシル 5%
ジエチルアミノヒドロキシベンゾイル安息香酸ヘキシル 2%
ビスエチルヘキシルオキシフェノールメトキシフェニルトリアジン 1%
イソドデカン 20%
ジメチルシリル化シリカ 1%
トリメチルシロキケイ酸 0.1%
ジフェニルシロキシフェニルトリメチコン 20%
ミリスチン酸イソプロピル 15%
アルコール 10%
パルミチン酸エチルヘキシル 残渣
Claims (7)
- (a)紫外線吸収剤と、
(b)屈折率が1.5~1.7の油分と、
(c)屈折率が1.3~1.5未満の油分と、
(d)屈折率が1.45~1.55の粉末と、
(e)油分増粘剤と
を含み、前記(b)屈折率が1.5~1.7の油分および前記(C)屈折率が1.3~1.5未満の油分の混合油分の屈折率が1.44~1.56であり、前記(e)油分増粘剤がデキストリン脂肪酸エステル、ショ糖脂肪酸エステル、グリセリル脂肪酸エステル、アミノ酸系ゲル化剤(ただし、リジン誘導体変性シリコーンを除く)脂肪酸もしくはその塩、または有機変性粘土鉱物である透明組成物。 - 前記アミノ酸系ゲル化剤が、ジブチルラウロイルグルタミド、ジブチルエチルヘキサノイルグルタミド、ポリアミド‐8またはポリアミド-3である請求項1記載の透明組成物。
- 前記(d)屈折率が1.45~1.55の粉末が、ポリメタクリル酸メチル、シリカ、ナイロン、セルロース、ポリエチレン、ポリウレタン、またはそれらを含む共重合体もしくは被覆処理体である請求項1または2記載の透明組成物。
- 前記(a)紫外線吸収剤に対する前記(d)屈折率が1.45~1.55の粉末の質量比が0.01以上1以下である請求項1、2または3記載の透明組成物。
- 固形である、請求項2~4いずれか1項記載の透明組成物。
- スティック状である、請求項5記載の透明組成物。
- 請求項1から6いずれか1項記載の透明組成物を基剤として含有する透明化粧料。
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CN109562035A (zh) | 2016-08-08 | 2019-04-02 | 株式会社资生堂 | 透明固体组合物 |
JP7294770B2 (ja) * | 2017-12-19 | 2023-06-20 | ロート製薬株式会社 | 皮膚外用組成物、紫外線吸収剤の機能低下抑制用組成物及び紫外線吸収剤の機能低下抑制方法 |
WO2020032242A1 (ja) * | 2018-08-10 | 2020-02-13 | 株式会社 資生堂 | 油性化粧料 |
WO2020088778A1 (en) * | 2018-11-02 | 2020-05-07 | Symrise Ag | A liquid and transparent blend of uv filters |
WO2021039617A1 (ja) * | 2019-08-26 | 2021-03-04 | 信越化学工業株式会社 | 固形化粧料 |
JPWO2021132018A1 (ja) * | 2019-12-27 | 2021-07-01 | ||
JP7354078B2 (ja) * | 2020-09-29 | 2023-10-02 | 富士フイルム株式会社 | 化粧料 |
FR3115457B1 (fr) * | 2020-10-23 | 2022-10-21 | Oreal | Composition photoprotectrice |
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KR102429950B1 (ko) | 2014-09-09 | 2022-08-04 | 가부시키가이샤 시세이도 | 입술용 고형 화장료 |
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WO2016068300A1 (ja) | 2014-10-31 | 2016-05-06 | 株式会社 資生堂 | 日焼け止め化粧料 |
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WO2017061604A1 (ja) * | 2015-10-09 | 2017-04-13 | 株式会社 資生堂 | 噴霧型日焼け止め化粧料 |
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2017
- 2017-04-26 JP JP2017087082A patent/JP7320914B2/ja active Active
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- 2018-04-12 WO PCT/JP2018/015402 patent/WO2018198800A1/ja unknown
- 2018-04-12 EP EP18792135.8A patent/EP3616679A4/en active Pending
- 2018-04-12 CN CN201880026759.3A patent/CN110573134B/zh active Active
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- 2018-04-12 KR KR1020197032176A patent/KR102735424B1/ko active IP Right Grant
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US20040185019A1 (en) * | 2003-02-11 | 2004-09-23 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Antiperspirant compositions |
JP2007314459A (ja) * | 2006-05-25 | 2007-12-06 | Shiseido Co Ltd | 透明固形組成物およびそれを基剤として含有する透明固形化粧料 |
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CN110573134B (zh) | 2023-03-21 |
KR102735424B1 (ko) | 2024-11-29 |
WO2018198800A1 (ja) | 2018-11-01 |
JP2018184370A (ja) | 2018-11-22 |
EP3616679A4 (en) | 2021-03-10 |
TW201841617A (zh) | 2018-12-01 |
EP3616679A1 (en) | 2020-03-04 |
KR20190136046A (ko) | 2019-12-09 |
CN110573134A (zh) | 2019-12-13 |
US20200375874A1 (en) | 2020-12-03 |
JP7320914B2 (ja) | 2023-08-04 |
US11413234B2 (en) | 2022-08-16 |
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