JP2013543002A - トリプシン活性を阻害又は低減するための化粧品組成物及び方法 - Google Patents
トリプシン活性を阻害又は低減するための化粧品組成物及び方法 Download PDFInfo
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Abstract
Description
本発明の実施形態は、N−アシルアミノ酸化合物とシクロヘキサン−1,2,3,4,5,6−ヘキソールとの混合物を含み、任意に、ビタミンB3化合物又は2−ヘキシルデカン−1−オールの1つ以上を更に含み得る。本発明者らは、驚くべきことに、N−アシルアミノ酸化合物とシクロヘキサン−1,2,3,4,5,6−ヘキソールとの組み合わせが、予想外に有利である程度まで又は個々の化合物によるよりも優れた程度までトリプシン活性を阻害することを発見した。本発明者らは、更に驚くべきことに、N−アシルアミノ酸化合物、シクロヘキサン−1,2,3,4,5,6−ヘキソール、ビタミンB3化合物、及び2−ヘキシルデカン−1−オールの組み合わせが、予想外に有利である程度まで又は個々の化合物によるよりも優れた程度までトリプシン活性を阻害することを発見した。
本発明の組成物は、安全かつ有効な量の1種以上のN−アシルアミノ酸化合物を含む。アミノ酸は、当該技術分野において既知のいかなるアミノ酸の1つでもあることができる。本発明のN−アシルアミノ酸化合物は、次式の化合物に相当する。
本発明の組成物は、次式に対応するシクロヘキサン−1,2,3,4,5,6−ヘキソール化合物の1種以上を安全かつ有効な量で含む。
本発明の組成物は、任意に、次式を有するビタミンB3化合物の1種以上を安全かつ有効な量で含み得る。
本発明の組成物は、一般にヘキシルデカノール(hexyldcanol)と呼ばれる2−ヘキシルデカン−1−オールを安全かつ有効な量で含む。本発明の組成物では、2−ヘキシルデカン−1−オールは、該組成物の約0.001%、約0.01%、若しくは約2.5%より大で、及び/又は約10%若しくは約5%未満で含まれる。
本発明の組成物は、組成物に、皮膚科学的に許容可能なキャリア(「キャリア」)も含むことができる。本明細書で使用するとき、「皮膚科学的に許容可能なキャリア」という語句は、該キャリアがケラチン組織への局所塗布に好適であり、良好な審美特性を有し、本発明の活性物質と適合性があり、安全性又は毒性についていかなる問題も起こさないことを意味する。一実施形態において、キャリアは、組成物の約50重量%〜約99重量%、約60重量%〜約98重量%、約70重量%〜約98重量%、又は代替的に約80重量%〜約95重量%のレベルで存在する。
以下の試験方法は、本発明の様々な実施形態の特定の特徴及び利点を説明するために提供されるものであり、本発明の範囲を限定するものとして解釈されるべきではない。
パーセント(%)トリプシン活性=[試験ウェルの勾配]/[ビヒクル対照ウェルの平均勾配] (1)
以下は、本発明の組成物の非限定的な実施例である。これらの実施例は単に説明のために示すものであり、本発明を限定するものと解釈すべきでなく、本発明の趣旨及び範囲から逸脱することなく、多くの改変が可能であり、当業者にはこれらのことが理解されよう。実施例においては、特に指定のない限り、全ての濃度が重量%として列挙されており、希釈剤、充填剤などの微量物質は除外し得る。そのため、列挙した配合は、列挙した成分及びこのような成分に関連するいかなる微量物質をも含む。当業者にとって明白なように、このような微量物質の選択は、本明細書に記載したように本発明を作るために選択した特定成分の物理的及び化学的特質によって変わることになる。
様々な治療方法が本発明の組成物を利用することができる。一実施形態において、該方法は、該組成物によって治療する1つ以上の加齢によるシミ又は不均一な皮膚色調を含む皮膚表面を識別する工程を含む。皮膚表面は、使用者、又は例えば皮膚科医、美容師、若しくは他の介護者等の第三者により識別されてもよい。識別は、寸法及び/又は色に基づいて、治療を必要とする皮膚表面の目視検査によって行われてもよい。識別はまた、SIAscope V(Astron Clinica,Ltd.,UKから入手可能)又はVISIA(登録商標)Complexion Analysisシステム(Canfield Scientific,Inc.,Fairfield,NJから入手可能)等の市販の画像化装置により行われてもよい。両方の装置は、皮膚の画像を収集し、加齢によるシミを識別することが可能である。
Claims (10)
- 皮膚への局所適用のために配合された化粧品組成物であって、
安全かつ有効な量、好ましくは前記化粧品組成物の2重量%〜3重量%のシクロヘキサン−1,2,3,4,5,6−ヘキソールと、
安全かつ有効な量の、N−アシルフェニルアラニン、N−アシルチロシン、それらの異性体、それらの塩、及びそれらの誘導体からなる群から選択されるN−アシルアミノ酸化合物、好ましくはウンデシレノイルフェニルアラニン、より好ましくはウンデシレノイルフェニルアラニンの濃度が前記化粧品組成物の0.2重量%〜1重量%であるウンデシレノイルフェニルアラニンと、
皮膚科学的に(dematologically)許容可能なビヒクルと、を含む化粧品組成物。 - ビタミンB3化合物、好ましくはナイアシンアミドを更に含み、より好ましくは、該ビタミンB3化合物の濃度が前記化粧品組成物の3重量%〜5重量%である、請求項1に記載の化粧品組成物。
- 2−ヘキシルデカン−1−オールを更に含み、好ましくは、前記2−ヘキシルデカン−1−オールの濃度が前記化粧品組成物の2.5重量%〜5重量%である、請求項1又は2に記載の化粧品組成物。
- 不均一な皮膚色調又は加齢によるシミを改善する、低減する、又は治療するための美容方法であって、
a)かかる治療が必要な皮膚表面を識別する工程と、
b)請求項1〜3のいずれか一項に記載の化粧品組成物を前記皮膚表面に局所的に塗布する工程と、
治療期間の間、前記皮膚表面の前記不均一な皮膚色調又は加齢によるシミを改善する、低減する、又は治療するのに十分な回数、工程b)を繰り返す工程と、を含む美容方法。 - 請求項1〜3のいずれか一項に記載の化粧品組成物を皮膚表面に局所的に塗布する工程を含む、皮膚表面におけるトリプシン活性を阻害又は低減するための美容方法。
- 治療期間の間、前記皮膚表面に前記化粧品組成物を局所的に塗布する工程を繰り返すことを更に含む、請求項4又は5に記載の美容方法。
- 前記治療期間が4〜12週間、好ましくは4〜10週間であり、かつ前記化粧品組成物を局所的に塗布する前記工程が、前記治療期間中少なくとも1日1回、好ましくは前記治療期間中少なくとも1日2回繰り返される、請求項4〜6のいずれか一項に記載の美容方法。
- 前記化粧品組成物が、前記治療期間の間、十分な量の前記化粧品組成物を収容するように寸法設定されたパッケージで提供される、請求項4〜7のいずれか一項に記載の美容方法。
- 前記化粧品組成物がローション又はクリームとして提供される、請求項4〜8のいずれか一項に記載の美容方法。
- 前記皮膚表面が顔の皮膚表面である、請求項4〜9のいずれか一項に記載の美容方法。
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JP2005521658A (ja) * | 2002-01-25 | 2005-07-21 | ソシエテ・デクスプロワタシオン・デ・プロデュイ・プール・レ・アンデュストリー・シミック・セピック | 皮膚を美白化するための化粧料的に許容され得る成分を含む組成物におけるプロテインキナーゼaを不活性化する化合物の使用 |
JP2006528935A (ja) * | 2003-07-25 | 2006-12-28 | ザ プロクター アンド ギャンブル カンパニー | N−アシルアミノ酸組成物を用いた哺乳類のケラチン組織の調整 |
JP2008150311A (ja) * | 2006-12-15 | 2008-07-03 | Lintec Corp | 水性ジェル組成物および水性ジェル貼付剤 |
WO2010088225A2 (en) * | 2009-01-29 | 2010-08-05 | The Procter & Gamble Company | Regulation of mammalian keratinous tissue using skin and/or hair care actives |
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Publication number | Publication date |
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KR20160017663A (ko) | 2016-02-16 |
WO2012068357A3 (en) | 2012-08-02 |
CN103298449A (zh) | 2013-09-11 |
WO2012068357A4 (en) | 2012-10-04 |
KR20130095300A (ko) | 2013-08-27 |
US20120148515A1 (en) | 2012-06-14 |
WO2012068357A2 (en) | 2012-05-24 |
JP5815728B2 (ja) | 2015-11-17 |
EP2640346A2 (en) | 2013-09-25 |
CA2818344C (en) | 2016-06-28 |
EP2640346B1 (en) | 2016-02-10 |
US8715628B1 (en) | 2014-05-06 |
KR101845224B1 (ko) | 2018-04-05 |
CA2818344A1 (en) | 2012-05-24 |
US8524204B2 (en) | 2013-09-03 |
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