JP2008539239A - 局所用組成物の蛍光検出 - Google Patents
局所用組成物の蛍光検出 Download PDFInfo
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- JP2008539239A JP2008539239A JP2008508970A JP2008508970A JP2008539239A JP 2008539239 A JP2008539239 A JP 2008539239A JP 2008508970 A JP2008508970 A JP 2008508970A JP 2008508970 A JP2008508970 A JP 2008508970A JP 2008539239 A JP2008539239 A JP 2008539239A
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- water
- fluorescent chromophore
- soluble
- sunscreen
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Abstract
【解決手段】1または複数種の油溶性または水溶性の紫外線保護剤および蛍光発色団を含む組成物であって、この蛍光発色団は、油溶性または水溶性で、約400nmを超える励起波長を有する、組成物(いわゆる昼光蛍光化合物)が第1の実施形態において開示されている。蛍光発色団と日焼け止め剤とを十分に混合して、単相組成物を生成するステップを含む、局所用組成物を製造する方法が開示されている。さらに、蛍光組成物と共に使用するための装置が記述され、この装置は、発光装置、光検出器、蛍光発色団の蛍光レベルを決定する電子評価システム、およびディスプレイシステムを含み、表面における前記組成物の存在を決定する。
【選択図】図1
Description
本発明は、局所用薬剤、および蛍光発色団を含む組成物、ならびに皮膚などの表面におけるこのような組成物の存在を検出するための方法および装置に関する。
スキンケアおよびヘアケア組成物や日焼け止め剤などの化粧品は、様々な利点を提供する。しかしながら、このような製品の利点は、適正な量使用することに大きく依存する。例えば、日焼け止め剤は、日光の紫外線による急性および慢性のダメージから皮膚を十分に保護する。このような効果を得るためには、消費者は、適正な量の日焼け止め剤を塗布しなければならない。研究結果から、消費者が塗布する日焼け止め剤の量が常習的に少ないため、日焼け止め剤使用による効果を制限していることが分かった。
本発明は、1または複数種の油溶性または水溶性の紫外線保護剤(ultraviolet sunscreen agents)および蛍光発色団を含む組成物を提供する。この蛍光発色団は、油溶性であって、約400nmを超える励起波長を有する。
特段の記載がない限り、本明細書で用いる全ての技術用語および科学用語は、本発明の属する技術分野の一般的な技術者が一般に理解する意味を有する。本明細書で言及する全ての刊行物、特許出願、特許、および他の参考文献は、参照して開示内容の全てを本明細書に組み入れる。本明細書で用いる「化合物」は、特段の記載がない限り、その全ての異性体(例えば、トコフェロール)を含む。
・3−ベンジリデンカンフル(3-benzylidene campher)、特に3−ベンジリデンノルカンフル(3-benzylidene norcampher)およびその誘導体、例えば、3−(4−メチルベンジリデン)カンフル
・4−アミノ安息香酸誘導体、特に4−(ジメチルアミノ)安息香酸−2−エチルヘキシルエステル、4−(ジメチルアミノ)安息香酸−2−オクチルエステル、および4−(ジメチルアミノ)安息香酸アミルエステル
・シナモン酸(cinnamonic acid)のエステル、特に4−メトキシシナモン酸−2−エチルヘキシルエステル(4-methoxycinnamonic acid-2- ethylhexylester)、4−メトキシシナモン酸プロピルエステル(4-methoxycinnamonicacid propylester)、4−メトキシシナモン酸イソアミルエステル(4-methoxycinnamonic acid isoamyl ester)、2−シアノ−3,3−フェニルシナモン酸−2−エチルヘキシルエステル(2-cyano-3,3-phenylcinnamonic acid-2-ethylhexyl ester)(オクトクレリン)
・サリチル酸エステル、すなわち、サリチル酸−2−エチルヘキシルエステル、サリチル酸−4−イソプロピルベンジルエステル、サリチル酸ホモメンチルエステル(salicylic acid homomenthyl ester)
・ベンゾフェノン誘導体、特に2−ヒドロキシ−4−メトキシベンゾフェノン、2−ヒドロキシ−4−メトキシ−4’−メチルベンゾフェノン、2,2’−ジヒドロキシ−4−メトキシベンゾフェノン
・ベンザルマロン酸エステル(esters of benzalmalonic acid)、特に4−メトキシベンズマロン酸ジ−2−エチルヘキシルエステル(4-methoxybenzmalonic acid di-2- ethylhexyl ester)
・トリアジン誘導体、例えば、2,4,6−トリアニリロ−(p−カルボ−2’−エチル−1’−ヘキシロキシ)−1,3,5−トリアジン(2,4,6-trianilino-(p-carbo-2'-ethyl-1'-hexyloxy)-1,3,5-triazine)およびオクチルトリアゾン(octyltriazone);または安息香酸、4,4’−[[6−[[[(1,1−ジメチルエチル)アミノ]カルボニル]フェニル]アミノ]−1,3,5−トリアジン−2,4−ジイル]ジイミノ]ビス−,ビス(2−エチルヘキシル)エステル(UVASORB HEB)(4,4'-[[6-[[[(1,1-dimethyletyl)amino]carbonyl]phenyl]amimo]-1,3,5-triazine-2,4-diyl]diimino]bis-,bis(2-ethylhexyl) ester (UVASORB HEB))
・プロパン−1,3−ジオン、例えば、1−(4−tert−ブチルフェニル)−3−(4’−メトキシフェニル)プロパン−1,3−ジオン(1-(4-tert.butylphenyl)-3-(4'-methoxyphenyl)propane-1,3-dione)
・ケトリサイクロ(5.2.1.0)デカン誘導体(Ketotricyclo(5.2.1.0)decane derivatives)
・2−フェニルベンズイミダゾール−5−スルホン酸(2-phenylbenzimidazol-5-sulfonic acid)およびそのアルカリ塩、アルカリ土類塩、アンモニウム塩、アルキルアンモニウム塩、アルカノールアンモニウム(alkanolammonium)塩、およびグルカンモニウム塩(glucammonium salts)
・ベンゾフェノンのスルホン酸誘導体、特に2−ヒドロキシ−4−メトキシベンゾフェノン−5−スルホン酸およびその塩
・3−ベンジリデンカンフル(3-benzylidene campher)のスルホン酸誘導体、例えば、4−(2−オキソ−3−ボルニリデンメチル)ベンゾスルホン酸(4-(2-oxo-3-bornylidene methyl)benzolsulfonic acid)および2−メチル−5−(2−オキソ−3−ボルニリデン)スルホン酸(2-methyl-5-(2-oxo-3-bornylidene)sulfonic acid)およびその塩
本発明に従った組成物は、カリフォルニア州ハンチントンビーチのリスク・リアクター社(Risk Reactor)が販売するDFSB−K43を0.1gだけ100gのSUNDOWN SPF60日焼け止め製品に添加して調製した。次に、この組成物を、PMMAプレートの研磨面の表面に0.5mg/cm2、1.0mg/cm2、1.5mg/cm2、2.0mg/cm2、および2.5mg/cm2(約1平方インチ(約6.5cm2)の試験部位)の密度で塗布した。塗布した日焼け止め剤中のDFSB−K43の蛍光を、450nmの放射線(単色光分光器からの)でDFSB−K43を励起して500nmの放出された蛍光を測定して求めることができる。試験部位における蛍光強度は、4回測定して、その結果を以下に示す表にプロットした。
同じサンプル調製物を、従来のインビトロSPF測定器具であるラブスフィアー社(Labsphere)のUV分光光度計を用いて測定して、塗布した密度サンプルのそれぞれのSPFを求めた。日焼け止め剤中の蛍光発色団の蛍光信号は、プレート上の製品のSPFと密接に相関することが示されている。
黄色色素43番を0.1%含むSPF 30 日焼け止め剤のサンプルを、約10分で乾燥できる1.6mg/cm2の密度でPMMAプレートの研磨面に塗布した。サンプルのSPFおよびサンプルからの蛍光信号を、上記したように分光蛍光計およびラブスフィアー社(Labsphere)のSPF分光光度計の両方で測定した。初めの測定の後で、サンプルを10秒〜15秒、強く流している水道水の下に置き、水流中で指の先で軽く擦り、再び測定を繰り返した。洗浄して擦った後の蛍光信号が低下しており、蛍光発色団の一部が除去されたことを示唆している。しかしながら、例2の線の傾斜が例1に類似しており(約12%以内)、蛍光発色団とUVフィルターがほぼ同じ割合で除去されていることを示唆している。これは、蛍光発色団とUVフィルターが互いに十分に結合し、かつ装置が、蛍光信号の変化から、UVフィルターの存在量の変化を予測できることを示している。
(1)1または複数種の油溶性または水溶性の紫外線保護剤、および蛍光発色団を含む組成物において、
前記蛍光発色団は、油溶性であって、約400nmを超える励起波長を有する、組成物。
(2)実施態様(1)に記載の組成物において、
前記蛍光発色団は、約1wt%未満の水への溶解度を有する、組成物。
(3)1または複数種の水溶性紫外線保護剤、および蛍光発色団を含む組成物において、
前記蛍光発色団は、水溶性であって、約400nmを超える励起波長を有する、組成物。
(4)局所用組成物を製造する方法において、
蛍光発色団と日焼け止め剤とを十分に混合して単相組成物を生成するステップ、
を含む、方法。
(5)実施態様(4)に記載の方法において、
希釈剤を前記日焼け止め剤および前記蛍光発色団に混合して前記単相組成物を生成するステップ、
をさらに含む、方法。
前記希釈剤は、1または複数種の疎水性物質を含む、方法。
(7)実施態様(5)に記載の方法において、
前記希釈剤は、水、アルコール、またはこれらの組合せを含む、方法。
(8)実施態様(4)に記載の方法において、
前記単相組成物に追加成分を添加して、安定した多相組成物を生成するステップ、
をさらに含む、方法。
(9)実施態様(8)に記載の方法において、
前記安定した多相組成物は、乳剤である、方法。
(10)実施態様(9)に記載の方法において、
前記乳剤は、油中水型相(a water exterior phase)または水中油型相(an oil exterior phase)を有する、方法。
(a)実施態様(1)に記載の組成物と、
(b)表面における前記組成物の存在を決定するための装置と、
を含み、
前記装置は、発光装置、光検出器、蛍光発色団の蛍光レベルを決定する電子評価システム、およびディスプレイシステムを含む、キット。
(12)実施態様(11)に記載のキットにおいて、
取扱説明書、
をさらに含む、キット。
(13)実施態様(11)に記載のキットにおいて、
前記局所用薬剤は、日焼け止め剤を含む、キット。
(14)キットにおいて、
(a)実施態様(3)に記載の組成物と、
(b)表面における前記組成物の存在を決定するための装置と、
を含み、
前記装置は、発光装置、光検出器、蛍光発色団の蛍光レベルを決定する電子評価システム、およびディスプレイシステムを含む、キット。
Claims (14)
- 1または複数種の油溶性または水溶性の紫外線保護剤、および蛍光発色団を含む組成物において、
前記蛍光発色団は、油溶性であって、約400nmを超える励起波長を有する、組成物。 - 請求項1に記載の組成物において、
前記蛍光発色団は、約1wt%未満の水への溶解度を有する、組成物。 - 1または複数種の水溶性紫外線保護剤、および蛍光発色団を含む組成物において、
前記蛍光発色団は、水溶性であって、約400nmを超える励起波長を有する、組成物。 - 局所用組成物を製造する方法において、
蛍光発色団と日焼け止め剤とを十分に混合して単相組成物を生成するステップ、
を含む、方法。 - 請求項4に記載の方法において、
希釈剤を前記日焼け止め剤および前記蛍光発色団に混合して前記単相組成物を生成するステップ、
をさらに含む、方法。 - 請求項5に記載の方法において、
前記希釈剤は、1または複数種の疎水性物質を含む、方法。 - 請求項5に記載の方法において、
前記希釈剤は、水、アルコール、またはこれらの組合せを含む、方法。 - 請求項4に記載の方法において、
前記単相組成物に追加成分を添加して、安定した多相組成物を生成するステップ、
をさらに含む、方法。 - 請求項8に記載の方法において、
前記安定した多相組成物は、乳剤である、方法。 - 請求項9に記載の方法において、
前記乳剤は、油中水型相または水中油型相を有する、方法。 - キットにおいて、
(a)請求項1に記載の組成物と、
(b)表面における前記組成物の存在を決定するための装置と、
を含み、
前記装置は、発光装置、光検出器、蛍光発色団の蛍光レベルを決定する電子評価システム、およびディスプレイシステムを含む、キット。 - 請求項11に記載のキットにおいて、
取扱説明書、
をさらに含む、キット。 - 請求項11に記載のキットにおいて、
前記局所用薬剤は、日焼け止め剤を含む、キット。 - キットにおいて、
(a)請求項3に記載の組成物と、
(b)表面における前記組成物の存在を決定するための装置と、
を含み、
前記装置は、発光装置、光検出器、蛍光発色団の蛍光レベルを決定する電子評価システム、およびディスプレイシステムを含む、キット。
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PCT/US2006/015314 WO2006118835A2 (en) | 2005-04-29 | 2006-04-21 | Topical composition fluorescence detection |
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EP (3) | EP1874261B1 (ja) |
JP (2) | JP5188958B2 (ja) |
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CN (3) | CN102053075B (ja) |
AT (1) | ATE489070T1 (ja) |
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US20100224795A1 (en) | 2010-09-09 |
KR20080063445A (ko) | 2008-07-04 |
US20100226861A1 (en) | 2010-09-09 |
JP2012103262A (ja) | 2012-05-31 |
WO2006118835A2 (en) | 2006-11-09 |
CA2605754C (en) | 2014-08-12 |
EP2275176A1 (en) | 2011-01-19 |
WO2006118835A3 (en) | 2007-04-12 |
BRPI0607683A2 (pt) | 2009-09-22 |
CN101198376A (zh) | 2008-06-11 |
JP5188958B2 (ja) | 2013-04-24 |
EP2275177A1 (en) | 2011-01-19 |
EP1874261B1 (en) | 2010-11-24 |
ATE489070T1 (de) | 2010-12-15 |
CN102053076A (zh) | 2011-05-11 |
DE602006018440D1 (de) | 2011-01-05 |
ES2535082T3 (es) | 2015-05-05 |
CN102053075B (zh) | 2014-06-04 |
CN102053075A (zh) | 2011-05-11 |
US20060246020A1 (en) | 2006-11-02 |
EP1874261A2 (en) | 2008-01-09 |
CA2605754A1 (en) | 2006-11-09 |
EP2275177B1 (en) | 2015-01-21 |
KR101367118B1 (ko) | 2014-02-26 |
JP5399464B2 (ja) | 2014-01-29 |
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