CN114650803A - 呈压实、耐冲击粉末形式的化妆品组合物 - Google Patents
呈压实、耐冲击粉末形式的化妆品组合物 Download PDFInfo
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- CN114650803A CN114650803A CN202080054012.6A CN202080054012A CN114650803A CN 114650803 A CN114650803 A CN 114650803A CN 202080054012 A CN202080054012 A CN 202080054012A CN 114650803 A CN114650803 A CN 114650803A
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Abstract
一种呈粉末形式的粉状组合物(C1),该粉状组合物对于100%其重量包含:i)按重量计从89.5%至94.65%的至少一种填充剂(FA);ii)按重量计从5%至10%的至少一种有色颜料(CP);iii)按重量计从0.35%至0.5%的至少一种交联的阴离子聚电解质类型的聚合物(P),其对于100mol%包含从65mol%至95mol%的衍生自部分或完全成盐的2‑甲基‑2‑[(1‑氧代‑2‑丙烯基)氨基]‑1‑丙磺酸的单体单元,从4.8mol%至25mol%的衍生自至少一种选自由以下构成的组的要素的中性单体的单体单元:丙烯酸2‑羟乙酯、甲基丙烯酸2‑羟乙酯、N,N‑二烷基丙烯酰胺——其中每个烷基包含一与四个之间的碳原子,以及从0.1mol%至5mol%的衍生自至少一种具有式(I)的单体的单体单元。
Description
本发明涉及一种组合物,该组合物包含至少一种填充剂、至少一种有色颜料,以及至少一种交联的阴离子聚电解质类型的聚合物,所述组合物在环境温度下呈粉状形式。
本发明还涉及一种呈压实形式的用于局部使用的化妆品组合物,其包含所述粉状组合物和至少一种粘合剂,展现出改善的耐冲击性。
本发明还涉及此类压实化妆品组合物作为用于化妆人体皮肤的产品的用途,以及一种用于使用此类压实组合物化妆人体皮肤的方法。
旨在用于化妆皮肤的某些用于局部使用的化妆品组合物,例如像用于面部的粉底、用于面部的粉饼、眼影或腮红,通常呈压实粉末或浇注粉末的形式。
出于本发明的目的,术语“压实粉末”应理解为意指主要由粉末的混合物组成的组合物,这些粉末包含至少一种填充剂、至少一种颜料、至少一种交联的阴离子聚电解质类型的聚合物、以及至少一种粘合剂。一旦形成,该混合物通过在罐中压实而成型。
这些压实粉末通常通过取少量并然后用手指或使用涂抹器例如像刷子或海绵将其施用至皮肤来使用。
优质的压实粉末要求其易于吸收,其易于涂抹,由此产生的涂抹是均匀的,并且涂抹在皮肤上后其具有柔软的手感。更具体地,优质的压实粉末必须具有光滑平整的表面,并且随着时间的推移保持其特性。优质的压实粉末还必须具有足够高的冲击强度以免碎裂并且以保持其特性。
为了改善冲击强度特性,旨在用于化妆皮肤的压实粉末的设计者基于特定粘合剂的优化开发了解决方案。
例如,以编号WO 9/17660 A1公开的国际专利申请描述了使用至少一种硅酮油、至少一种硅酮蜡,以及至少一种硅酮树脂的混合物,构成脂肪粘合剂,其旨在与固体微粒相混合以便随后获得压实粉末。然而,待使用的粘合剂的量被证明是显著的,并且压实粉末的表面外观然后变得油性并且在施用前转移到手指或涂抹器的效率更低。
以编号EP 0 171 979 A2公开的欧洲专利申请描述了一种用于制备组合物的方法,该组合物采用压实、储存稳定、耐冲击粉末的形式,其特征在于平整光滑的表面。形成欧洲专利申请EP 0 717 979 A2的主题方法包括将粉状相分散在预先形成的水包油乳液中的步骤,然后是将获得的分散体浇铸到模具中的步骤,以及然后是通过冻干来干燥先前获得的分散体的步骤。然而,此种方法具有难以在工业规模上实施的缺点,因为该方法涉及消耗大量能量的昂贵设备。
以编号US 2005/0186235 A1公开的美国专利申请描述了这样的化妆品组合物,其采用压实粉末形式并且包含粉状相、固体脂肪相,并且为了其制备需要实施被证明是非常耗能的熔化固体脂肪相(或蜡)的步骤。
以编号US 2016/167040 A1公开的美国专利申请描述了交联的阴离子聚电解质类型的聚合物,其聚合物骨架由用三羟甲基丙烷三丙烯酸酯交联的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸(ATBS)的铵盐、丙烯酸(2-羟乙基)酯(HEA)、甲基丙烯酸硬脂酯(SMA)以及甲基丙烯酸月桂酯(LAUMA)(ATBS/HEA/SMA/LAUMA:88.1/9.9/1.5/0.5;聚电解质1)组成。以编号US 2016/167040 A1公开的美国专利申请也描述了一种压实粉末的化妆品组合物(实例52),其包含按质量计2%的聚电解质1。
以编号FR 2980108 A1公开的法国专利申请描述了呈压实、耐冲击粉末形式的彩妆组合物,其包含粉状相和液相,但不含交联的阴离子聚电解质类型的聚合物。
为了克服这些缺点,诸位发明人已经设法提供一种化妆品组合物,其采用压实、耐冲击粉末的形式,特征在于用于促进吸收和施用至皮肤的良好转移品质,并且根据不需要输入大量能量的方法来制备。
因此,本发明的主题是一种呈粉末形式的粉状组合物(C1),该粉状组合物每100%其质量包含:
i)按质量计从84.3%至95.8%、优选地按质量计从86.9%至95.2%、并且甚至更优先地按质量计从89.5%至94.65%的至少一种填充剂(FA)
ii)按质量计从4%至15%、优选地按质量计从4.5%至12.5%、并且甚至更优先地按质量计从5%至10%的至少一种有色颜料(CP)
iii)按质量计从0.2%至0.7%、优选地按质量计从0.3%至0.6%、并且甚至更优先地按质量计从0.35%至0.5%的至少一种交联的阴离子聚电解质类型的聚合物(P),该至少一种交联的阴离子聚电解质类型的聚合物衍生自在至少一种交联剂的存在下的部分或完全成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸与至少一种选自由丙烯酸2-羟乙酯、甲基丙烯酸2-羟乙酯、N,N-二烷基丙烯酰胺(其中每个烷基包含在一与四个之间的碳原子)组成的组的要素的中性单体,和至少一种具有式(I)的单体的聚合,该具有式(I)的单体:
[化学式1]
其中R表示直链或支链的包含从八至二十个碳原子的烷基,并且n表示大于或等于零且小于或等于二十的数。
出于本发明的目的,术语“填充剂”应理解为意指与水不混溶并分散在基质中的固体化学物质。将填充剂引入混合物中,在此情况下为彩妆组合物,以便改善其成本以及某些特性,例如像在皮肤上的覆盖力或粉状组合物的密度。
根据更具体的方面,粉状组合物(C1)包含按体积计至少90%的直径小于或等于200微米、并且更特别地直径小于或等于100微米的颗粒。在本发明的上下文中,这意指粉末组合物C1与颗粒的粉末相当,这些颗粒与其直径小于或等于200微米、并且更特别地其直径直径小于或等于100微米的球体相当。应该注意的是,这种尺寸的颗粒使得随后获得的压实粉末可以获得更好的内聚力。
此参数借助于激光衍射分析仪确定,例如Malvern MastersizeTM 2000激光粒度仪,该粒度仪配备有分散装置,例如MS1-Small Volume Sample DispersionTM类型的分散装置,并连接到计算软件上,这使得可以获得由所分析粉末中呈现的每种尺寸的颗粒的衍射图像的叠加组成的衍射图。
在分析如此收集的数据时,估计初始尺寸分布并计算理论衍射图,并且然后将其与记录的实际数据进行比较。随后使用最小二乘法将估计数据与实际数据之间的差最小化。软件随后将体积分布计算为基本结果,并假设颗粒具有球形形状,则从该结果推导出任何其他信息。
这种测定方法特别很好地适合于粉末的表征,其中构成它们的颗粒与具有在3000微米与0.1微米之间的直径的球体相当,并且适合于干粉末。对于大于10微米的颗粒尺寸,此类型方法的使用特别地已经示出了良好的结果[P.Bowen,“Particle SizeDistribution Measurement from Millimeters to Nanometers and from Rods toPlatelets[从毫米至纳米以及从棒至片晶的颗粒尺寸分布测量]”;J.Dispersion Scienceand Technology[分散科学与技术杂志],23(5),第631-662页(2002)]。
在粉状组合物(C1)的定义中,术语“交联的阴离子聚电解质类型的聚合物(P)”表示非线性的交联的阴离子聚电解质,其呈不溶于水但在水中溶胀的三维网络的形式并且因此导致化学凝胶的产生。
在粉状组合物(C1)的定义中,术语“部分成盐或完全成盐”意指2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸的酸官能团是部分或完全成盐的,通常是呈碱金属盐的形式,例如钠盐或钾盐,或呈铵盐的形式。
在如上定义的并且作为本发明的主题的粉状组合物(C1)中,使用的所述交联的阴离子聚电解质类型的聚合物(P)每100mol%总体上包含在65mol%与95mol%之间、更特别地在65mol%与90mol%之间、并且甚至更特别地在68mol%与95mol%之间、并且甚至更特别地在70mol%与95mol%之间、并且甚至更特别地在70mol%与90mol%之间的衍生自部分或完全成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸的单体单元。
在如上定义的并且作为本发明的主题的粉状组合物(C1)中,使用的所述交联的阴离子聚电解质类型的聚合物(P)每100mol%总体上包含在4.8mol%与25mol%之间、更特别地在4.8mol%与20mol%之间、并且甚至更特别地在5mol%与20mol%之间的至少一种选自由丙烯酸2-羟乙酯、甲基丙烯酸2-羟乙酯、N,N-二烷基丙烯酰胺(其中每个烷基包含在一与四个之间的碳原子)组成的组的要素的中性单体的单体单元。
根据具体方面,在作为本发明的主题的粉状组合物(C1)中使用的交联的阴离子聚电解质类型的聚合物(P)中,选自N,N-二烷基丙烯酰胺(其中每个烷基包含在一与四个之间的碳原子)的中性单体选自N,N-二甲基丙烯酰胺、N,N-二乙基丙烯酰胺和N,N-二丙基丙烯酰胺。
在如上定义的并且作为本发明的主题的粉状组合物(C1)中,使用的所述交联的阴离子聚电解质类型的聚合物(P)每100mol%总体上包含在0.1mol%与10mol%之间、更特别地在0.1mol%与5mol%之间、并且甚至更特别地在0.1mol%与4.0mol%之间的至少一种具有式(I)的单体的单体单元。
在作为本发明的主题的粉状组合物(C1)中使用的所述交联的阴离子聚电解质类型的聚合物(P)中存在的单体的式(I)中,“直链或支链的包含从八至二十个碳原子的烷基”更特别地表示,对于R:
-或者衍生自直链伯醇的基团,例如辛基、癸基、十一烷基、十二烷基、十三烷基、十四烷基、十五烷基、十六烷基、十七烷基、十八烷基、十九烷基或二十烷基;
-或者衍生自格尔伯特(Guerbet)醇的基团,其为对应于以下通式的支链1-烷醇:
CH3-(CH2)p-CH[CH3-(CH2)p-2]-CH2OH,
其中p表示在2与9之间的整数,例如2-乙基己基、2-丙基庚基、2-丁基辛基、2-戊基壬基、2-己基癸基或2-辛基十二烷基;
-或者衍生自对应于以下通式的异烷醇的基团:
CH3-CH(CH3)-(CH2)m-CH2OH,
其中m表示在2与16之间的整数,例如4-甲基戊基、5-甲基己基、6-甲基庚基、15-甲基十五烷基或16-甲基十七烷基、或2-己基辛基、2-辛基癸基或2-己基十二烷基。根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于所述交联的阴离子聚电解质类型的聚合物(P)每100mol%包含:
-从65mol%至95mol%、优选地从70mol%至95mol%的衍生自部分或完全成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸的单体单元;
-从4.8mol%至25mol%、优选地从4.8mol%至20mol%的衍生自选自由丙烯酸2-羟乙酯、甲基丙烯酸2-羟乙酯、N,N-二烷基丙烯酰胺(其中每个烷基包含在一与四个之间的碳原子)组成的组的要素的中性单体的单体单元;
-从0.1mol%至5mol%、优选地从0.5mol%至5mol%、并且更优先地从0.5mol%至4mol%的衍生自如上定义的具有式(I)的单体的单体单元,
-从0.1mol%至5mol%、优选地从0.5mol%至5mol%、并且更优先地从0.5mol%至3mol%的衍生自至少一种二烯属或多烯属交联单体的单体单元。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于,在交联的阴离子聚电解质类型的聚合物(P)中,所述中性单体选自由丙烯酸2-羟乙酯或N,N-二甲基丙烯酰胺组成的组的要素。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于,在所述交联的阴离子聚电解质类型的聚合物(P)中和对于如上定义的所述具有式(I)的单体,R表示包含从12至18个碳原子的烷基。
根据另一个具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于,在所述交联的阴离子聚电解质类型的聚合物(P)中,R表示正十二烷基或异十二烷基或正十四烷基或正十六烷基或正十八烷基,并且n表示在3与20之间的整数。
根据另一个具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于,在所述交联的阴离子聚电解质类型的聚合物(P)中,如上定义的所述具有式(I)的单体是具有式(I1)的四乙氧基化的甲基丙烯酸月桂酯,其对应于其中n等于四并且R表示正十二烷基的式(I)。
根据另一个具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于,在所述交联的阴离子聚电解质类型的聚合物(P)中,如上定义的所述具有式(I)的单体是具有式(I4)的二十乙氧基化的甲基丙烯酸硬脂酯,其对应于其中n等于二十并且R表示正十八烷基的式(I)。
根据另一个具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于,在所述交联的阴离子聚电解质类型的聚合物(P)中,R表示正十二烷基或异十二烷基或正十四烷基或正十六烷基或正十八烷基,并且n等于零。
根据另一个具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于,在所述交联的阴离子聚电解质类型的聚合物(P)中,如上定义的所述具有式(I)的单体是具有式(I2)的甲基丙烯酸月桂酯,其对应于其中R表示正十二烷基和/或异十二烷基并且其中n等于零的式(I)。
根据另一个具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于,在所述交联的阴离子聚电解质类型的聚合物(P)中,如上定义的所述具有式(I)的单体是具有式(I3)的甲基丙烯酸硬脂酯,其对应于其中R表示正十八烷基并且n等于零的式(I)。
根据更具体的方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于,在所述交联的阴离子聚电解质类型的聚合物(P)中,所述具有式(I)的单体选自由以下组成的组的要素:具有式(I1)的四乙氧基化的甲基丙烯酸月桂酯,其对应于其中R表示正十二烷基并且其中n等于四的式(I),具有式(I2)的甲基丙烯酸月桂酯,其对应于其中R表示正十二烷基并且其中n等于零的式(I),具有式(I’2)的甲基丙烯酸异癸酯,其对应于其中R表示异十二烷基并且其中n等于零的式(I),以及具有式(I3)的甲基丙烯酸硬脂酯,其对应于其中R表示正十八烷基并且其中n等于零的式(I)。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于,在所述交联的阴离子聚电解质类型的聚合物(P)中,所述二烯属或多烯属交联单体选自乙二醇二甲基丙烯酸酯、四烯丙氧基乙烷、乙二醇二丙烯酸酯、二烯丙基脲、三烯丙基胺、三羟甲基丙烷三丙烯酸酯、亚甲基双(丙烯酰胺),或这些化合物的混合物。
如上所述的粉状组合物(C1)中使用的交联的阴离子聚电解质(P)还可以包含各种添加剂,如络合剂、转移剂或链限制剂。
术语“转移剂”或“链限制剂”表示这样的化合物,当在用于制备交联的阴离子聚电解质(P)的自由基聚合反应期间存在时,这些化合物产生终止反应,如歧化或重组反应,导致形成长度较短并因此分子量较低的聚合物链。作为转移剂或链限制剂,可以提及硫醇如十二烷基硫醇、卤化物如四氯化碳、短链醇如乙醇、正丙醇、异丙醇、正丁醇或异丁醇,以及具有化学式NaPO2H2的次磷酸钠。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于所述交联的阴离子聚电解质类型的聚合物(P)选自用三羟甲基丙烷三丙烯酸酯交联的以铵盐形式部分成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸、N,N-二甲基丙烯酰胺和四乙氧基化的甲基丙烯酸月桂酯的聚合物,或选自用三羟甲基丙烷三丙烯酸酯交联的以铵盐形式部分成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸、N,N-二甲基丙烯酰胺和二十乙氧基化的甲基丙烯酸硬脂酯的聚合物。
根据甚至更具体的方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于所述交联的阴离子聚电解质类型的聚合物(P)是用三羟甲基丙烷三丙烯酸酯交联的以铵盐形式部分或完全成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸、N,N-二甲基丙烯酰胺以及具有式(I1)的四乙氧基化的甲基丙烯酸月桂酯的聚合物。
根据甚至更具体的方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于所述交联的阴离子聚电解质类型的聚合物(P)每100mol%包含:
-从65mol%至95mol%的衍生自以铵盐形式成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸的单体单元;
-从4.8mol%至25mol%的衍生自N,N-二甲基丙烯酰胺的单体单元,
-从0.1mol%至5mol%的衍生自具有式(I1)的四乙氧基化的甲基丙烯酸月桂酯的单体单元,
-从0.1mol%至5mol%的衍生自三羟甲基丙烷三丙烯酸酯的单体单元。
根据甚至更具体的方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于所述交联的阴离子聚电解质类型的聚合物(P)是以钠盐形式部分或完全成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸,丙烯酸2-羟乙酯,以大于或等于1/10且小于或等于10/1的(I2)/(I3)或(I’2)/(I3)的摩尔比的具有式(I2)的甲基丙烯酸月桂酯或具有式(I’2)的甲基丙烯酸异癸酯的和具有式(I3)的甲基丙烯酸硬脂酯的并用三羟甲基丙烷三丙烯酸酯交联的聚合物。
根据甚至更具体的方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于所述交联的阴离子聚电解质类型的聚合物(P)每100mol%包含:
-从70mol%至95mol%的衍生自以钠盐形式成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸的单体单元;
-从4.8mol%至20mol%的衍生自丙烯酸2-羟乙酯的单体单元,
-从0.1mol%至5mol%的衍生自以大于或等于1/6且小于或等于6/1的(I2)/(I3)或(I’2)/(I3)的摩尔比的具有式(I2)的甲基丙烯酸月桂酯或具有式(I’2)的甲基丙烯酸异癸酯和衍生自具有式(I3)的甲基丙烯酸硬脂酯的单体单元,
-从0.1mol%至5mol%的三羟甲基丙烷三丙烯酸酯。
交联的阴离子聚电解质类型的聚合物(P)可以通过实施包括以下的方法获得:
-步骤a),在该步骤期间,将所有单体、用于2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸的含氨中和剂、交联剂以及,如有必要或者如有需要,其他添加剂在有机溶剂、优选地叔丁醇中混合;
-步骤b),在该步骤期间,聚合反应通过将自由基引发剂引入步骤a)中制备的分散体中来引发,并然后继续进行直至该聚合反应完成;
-任选地步骤c):用钠离子或钾离子交换存在的铵离子;
-步骤d):沉淀在步骤b)、任选地步骤c)结束时形成的聚合物;
-任选地步骤e):干燥在步骤d)结束时获得的沉淀物。
作为在如上定义的方法的步骤a)中使用的含氨中和剂,例如有氨或碳酸氢铵。
在如上定义的方法的步骤b)中,聚合反应在通常等于或大于50℃的温度下使用通过均裂产生自由基的自由基引发剂引发,这些自由基引发剂如过氧化二月桂酰、偶氮二(异丁腈)或偶氮衍生物。
根据如上定义的方法的另一个实施例,聚合反应由氧化还原对引发。
在如上定义的方法的步骤c)中,铵阳离子与钠阳离子或与钾阳离子的交换任选地是用叔丁醇钠或叔丁醇钾进行。
在如上定义的方法的步骤d)中,交联的阴离子聚电解质(P)的沉淀是通过蒸发溶剂或通过过滤沉淀物来进行。
然后将由此获得的交联的阴离子聚电解质(P)在至少一种有色颜料和至少一种填充剂的存在下引入碾磨机,例如像刀磨机中,以便获得研磨粉末的混合物。
将该粉状混合物在至少一种粘合剂的存在下引入金属罐中,并然后使其经受通过机器在合适的压力下压实的步骤。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于该填充剂(FA)选自由以下组成的组的要素:无机层状类型的填料、有机层状类型的填料、无机球形类型的填料和有机球形类型的填料。
每种类型的填料使能够赋予根据本发明的组合物(C1)特别的和不同的品质。因此,例如,无机层状类型的填料通常提供柔软性,无机球形类型的填料通常提供良好的崩解性,并且有机球形填料通常具有结构化作用并提供柔软性。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于填充剂(FA)是选自由以下组成的组的要素的无机层状类型的填料:滑石或水合硅酸镁;云母或硅铝酸盐,例如像白云母、珍珠云母、钒云母、锂云母、黑云母;粘土,例如像绢云母;高岭土或水合硅酸铝;以及氮化硼。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于填充剂(FA)是选自由四氟乙烯聚合物粉末和月桂酰赖氨酸组成的组的要素的有机层状类型的填料。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于填充剂(FA)是无机球形类型的填料,其选自由以下组成的组的要素:锌氧化物、钛氧化物、碳酸钙、碳酸镁、碳酸氢镁、无孔球形二氧化硅、羟磷灰石、具有开放孔隙率的二氧化硅微球、中空二氧化硅微球、玻璃微胶囊、和陶瓷微胶囊。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于填充剂(FA)是有机球形类型的填料,其选自由以下组成的组的要素:衍生自具有从8至22个碳原子的有机羧酸的金属皂,例如像硬脂酸锌、硬脂酸镁、硬脂酸锂、月桂酸锌、肉豆蔻酸镁;未膨胀的合成聚合物粉末,例如像聚乙烯粉末,聚酯粉末例如像聚间苯二甲酸乙二醇酯粉末或聚对苯二甲酸乙二醇酯粉末,聚酰胺粉末;交联的或未交联的合成聚合物粉末,例如像聚丙烯酸粉末、聚甲基丙烯酸粉末、与二乙烯基苯交联的聚苯乙烯的粉末、硅酮树脂粉末;玉米淀粉、小麦淀粉、木薯淀粉或稻米淀粉粉末;丙烯酸类聚合物微球、聚甲基丙烯酸甲酯微球、和苯乙烯-二乙烯苯共聚物微球。
根据更具体的方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于填充剂(FA)选自由以下组成的组的要素:
-无机层状层状类型的填料,其选自由以下组成的组:滑石或水合硅酸镁;云母或硅铝酸盐,例如像白云母、珍珠云母、钒云母、锂云母、黑云母;粘土,例如像绢云母;高岭土或水合硅酸铝;以及氮化硼,
-有机层状类型的填料,例如像四氟乙烯聚合物粉末和月桂酰赖氨酸,
-无机球形类型的填料,其选自由以下组成的组的要素:锌氧化物、钛氧化物、碳酸钙、碳酸镁、碳酸氢镁、无孔球形二氧化硅、羟磷灰石、具有开放孔隙率的二氧化硅微球、中空二氧化硅微球、玻璃微胶囊、和陶瓷微胶囊,
-有机球形类型的填料,其选自由以下组成的组的要素:衍生自具有从8至22个碳原子的有机羧酸的金属皂,例如像硬脂酸锌、硬脂酸镁、硬脂酸锂、月桂酸锌、肉豆蔻酸镁;未膨胀的合成聚合物粉末,例如像聚乙烯粉末,聚酯粉末例如像聚间苯二甲酸乙二醇酯粉末或聚对苯二甲酸乙二醇酯粉末,聚酰胺粉末;交联的或未交联的合成聚合物粉末,例如像聚丙烯酸粉末、聚甲基丙烯酸粉末、与二乙烯基苯交联的聚苯乙烯的粉末、硅酮树脂粉末;玉米淀粉、小麦淀粉、木薯淀粉或稻米淀粉粉末;丙烯酸类聚合物微球、聚甲基丙烯酸甲酯微球、和苯乙烯-二乙烯苯共聚物微球。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于有色颜料(CP)选自由以下组成的组的要素:无机颜料、有机颜料和珠光颜料。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于有色颜料(CP)是无机颜料,其选自由以下组成的组的要素:二氧化钛(金红石或锐钛矿),任选地经表面处理;黑色、黄色、红色和棕色铁氧化物;锰紫;群青蓝;任选地水合氧化铬;铁蓝。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于有色颜料(CP)是有机颜料,其选自由以下组成的组的要素:D&C红色颜料、D&C橙色颜料、D&C黄色颜料、炭黑、基于胭脂虫红的色淀。
根据具体方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于有色颜料(CP)是珠光颜料,其选自由以下组成的组的要素:白色珠光颜料,例如像具有铁氧化物的氧化钛涂覆的云母、具有铁蓝或氧化铬的氧化钛涂覆的云母,具有有机颜料的氧化钛涂覆的云母,基于氯氧化铋的颜料。
根据更具体的方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于有色颜料(CP)选自由以下组成的组的要素:
-无机颜料,其选自由以下组成的组的要素:二氧化钛(金红石或锐钛矿),任选地经表面处理;黑色、黄色、红色和棕色铁氧化物;锰紫;群青蓝;任选地水合氧化铬;铁蓝,
-有色颜料,其选自由以下组成的组的要素:D&C红色颜料、D&C橙色颜料、D&C黄色颜料、炭黑、基于胭脂虫红的色淀,
-珠光颜料,其选自由以下组成的组的要素:白色珠光颜料,例如像具有铁氧化物的氧化钛涂覆的云母、具有铁蓝或氧化铬的氧化钛涂覆的云母,具有有机颜料的氧化钛涂覆的云母,基于氯氧化铋的颜料。
根据更具体的方面,本发明的主题是如上所述的粉状组合物(C1),其特征在于该粉状组合物每100%其质量包含,按质量计小于或等于2%、优选地按质量计小于或等于1.5%、并且甚至更优先地按质量计小于或等于1%的按质量计的含量的水。
根据第二方面,本发明的主题是用于局部使用的组合物(F),该组合物每100%其质量包含:
-按质量计从90%至97%、优选地按质量计从92.5%至96.5%、并且甚至更优先地按质量计从94%至96%的至少一种如上定义的粉状组合物(C1),
-按质量计从3%至10%、优选地按质量计从3.5%至7.5%、并且甚至更特别地按质量计从4%至6%的至少一种在20℃下为液体的脂肪粘合剂(BA)。
在组合物(F)的定义中使用的表述“用于局部使用”意指所述用于局部使用的组合物通过施用于身体和面部皮肤、头发、头皮或粘膜使用,无论这是在化妆品、皮肤化妆品、皮肤药物或药物配制品的情况下的直接施用,还是例如在呈纺织品或纸擦拭物形式的身体卫生产品或旨在与皮肤或粘膜接触的卫生产品的情况下的间接施用。
在本发明的上下文中,术语“脂肪粘合剂”表示脂肪、亲脂性化学组合物或物质,其功能是将呈粉末或粒料形式的颗粒聚集成固体块,以便减少其在冲击作用下破碎风险,并确保其易于吸收。
根据具体的方面,本发明的主题是如上所述的用于局部使用的组合物(F),其特征在于脂肪粘合剂(BA)选自由以下组成的组的要素:
i)包含至少一种硅酮油、至少一种硅酮蜡和至少一种硅酮树脂,以及任选地至少一种硅酮胶和至少一种苯基聚二甲基硅氧烷的组合物,如以编号WO 93/17660 A1公开的国际专利申请中所定义的,
ii)在20℃为液体的支链烷烃,例如像异十二烷或2,2,4,6,6-五甲基庚烷(CAS号:31807-55-3/93685-81-5/13475-82-6),异十六烷CAS=(93685-80-4)或2,2,4,4,6,8,8-七甲基壬烷(CAS=4390-04-9),
iii)在20℃和大气压下为液体的矿物油,例如像液体石蜡,非支链烷烃例如像正癸烷、正十一烷、正十二烷、正十三烷、正十四烷、正十五烷、正十六烷、正十七烷,
iv)基于甘油单酯和/或甘油二酯和/或甘油三酯的植物来源的油,其表示包含具有式(A1)和/或具有式(A’1)的甘油单酯,和/或具有式(A2)和/或具有式(A’2)的甘油二酯,和/或具有式(A3)的甘油三酯的化学物质,对于这些化学物质,其制备所需的原料是植物:
CH3-(CH2)x1-C(O)-O-CH2-CH(OH)-CH2-OH(A1)
HO-CH2-CH[O-C(O)-(CH2)x2-CH3]-CH2-O-H(A’1)
CH3-(CH2)x3-C(O)-O-CH2-CH(OH)-CH2-O-C(O)-(CH2)x4-CH3(A2)
CH3-(CH2)x5-C(O)-O-CH2-CH[O-C(O)-(CH2)x6-CH3]-CH2-O-H(A’2)
CH3-(CH2)x7-C(O)-O-CH2-CH[O-C(O)-(CH2)x8-CH3]-CH2-O-C(O)-(CH2)x9-CH3(A3)
其中x1、x2、x3、x4、x5、x6、x7、x8和x9,可以相同或不同,表示在7与23之间的整数。
在如上定义的基于甘油单酯和/或甘油二酯和/或甘油三酯的植物来源的油之中,可以提及例如甜杏仁油、椰仁油、蓖麻油、橄榄油、菜籽油、花生油、向日葵油、小麦胚芽油、玉米胚芽油、大豆油、棉籽油、苜蓿油、罂粟籽油、南瓜籽油、菘蓝油、琉璃苣油、月见草油、小米油、大麦油、黑麦油、红花油、烛果油、西番莲油、榛子油、棕榈油、牛油树油、杏仁油、胡桐油(calophyllum oil)、水蒜芥油(sisymbrium oil)、鳄梨油、金盏花油、火麻油(hempoil)、衍生自花的油、衍生自蔬菜的油、通过在植物来源的脂肪酸与甘油之间的酯化反应获得的甘油三酯,例如像三异硬脂酸甘油酯、由迪博斯特林公司(Stéarinerie Dubois)以名称DUB MCT出售的辛酸/癸酸甘油三酯、由迪博斯特林公司以名称DUB THG出售的通过在包含七个碳原子的脂肪酸与甘油之间的酯化反应获得的甘油三酯、由禾大公司(Croda)以名称Syncrowax HRC出售的通过在包含22个碳原子的脂肪酸与甘油之间的酯化反应获得的甘油三酯。
v)在20℃为液体的脂肪酯,例如像新戊酸异硬脂酯、癸酸二辛酯、异鲸蜡醇硬脂酸酯、肉豆蔻酸异丙酯、己二酸十六烷基酯,
vi)具有式(II)的异烷醇:
(CH3)(CH3)CH-(CH2)r-CH2-OH(II),
在该式(II)中,r表示在8与20之间的整数,例如异癸基、异十一烷基、异十二烷基、异十三烷基、异十四烷基、异十五烷基、
异十六烷基、异十五烷基、异十八烷基、异十九烷基、异二十烷基或异二十二烷基;
vii)具有式(III)的格尔伯特醇:
CH(CsH2s+1)(CtH2t+1)-CH2-OH(III)
在该式(III)中,t是在6与18之间的整数,s是介于4与18之间的整数,并且s+t之和大于或等于10且小于或等于22,例如2-丁基辛基、2-丁基癸基、2-己基辛基、2-己基癸基、2-辛基癸基、2-己基十二烷基、2-辛基十二烷基、2-癸基十四烷基、2-十二烷基十六烷基或2-十四烷基十八烷基,
viii)在20℃为液体的脂肪醇,例如像油醇或(Z)-十八碳-9-烯-1-醇,亚油醇或顺,顺-9,12-十八碳二烯-1-醇,亚麻醇或(9Z,12Z,15Z)-9,12,15-十八碳三烯-1-醇,
ix)硅酮衍生物,例如像聚二甲基硅氧烷、环戊硅氧烷、乙烯基聚二甲基硅氧烷、辛基聚甲基硅氧烷、二苯基聚二甲基硅氧烷。
根据具体的方面,在20℃下为液体的脂肪粘合剂(BA)选自由以下组成的组的要素:聚二甲基硅氧烷、环戊硅氧烷、乙烯基聚二甲基硅氧烷、辛基聚甲基硅氧烷、二苯基聚二甲基硅氧烷、异十六烷、异十二烷、液体石蜡、蓖麻油、甜杏仁油、澳洲坚果油、癸酸/辛酸甘油三酯、癸酸二辛酯、异硬脂醇新戊酸酯、辛基十二烷醇、己基癸醇。
根据更具体的方面,脂肪粘合剂选自由以下组成的组的要素:蓖麻油、辛基十二烷醇、聚二甲基硅氧烷、鲸蜡硬脂醇乙基己酸酯,以及肉豆蔻酸异丙酯。
作为本发明的主题的用于局部使用的组合物(F)特别地呈腮红、眼影、用于化妆脸部的粉末、(有香味的和/或除臭)身体粉末,包括用于脚和手的粉末的形式。
呈压实粉末形式并且作为本发明的主题的用于局部使用的组合物(F)可以包含这样的添加剂,这些添加剂在特别是化妆品、皮肤化妆品、药物或皮肤药物、用于局部使用的配制品的领域中常用,并且选自抗菌剂、收敛剂、防晒剂、愈合剂、自由基清除剂、维生素;缓和剂、润肤剂、保湿剂(甘油、山梨醇等)、皮肤美白剂、香料、稠度剂。
作为任选地存在于作为本发明的主题的用于局部使用的组合物(F)中的除臭剂的实例,可以提及碱金属硅酸盐,锌盐,如硫酸锌、葡萄糖酸锌、氯化锌或乳酸锌;季铵盐,如鲸蜡基三甲基铵盐或鲸蜡基吡啶盐;甘油衍生物,如甘油癸酸酯、甘油辛酸酯或聚甘油癸酸酯;1,2-癸二醇、1,3-丙二醇;水杨酸;碳酸氢钠;环糊精;金属沸石;TriclosanTM;水合溴化铝,水合氯化铝,氯化铝,硫酸铝,水合氯化铝锆,水合三氯化铝锆,水合四氯化铝锆,水合五氯化铝锆,水合八氯化铝锆,硫酸铝,乳酸钠铝,或水合氯化铝和二醇的络合物,如水合氯化铝和丙二醇的络合物,水合二氯化铝和丙二醇的络合物,倍半氯化羟基铝和丙二醇的络合物,水合氯化铝和聚乙二醇的络合物,水合二氯化铝和聚乙二醇的络合物,或倍半氯化羟基铝和聚乙二醇的络合物。
在可以包括在作为本发明主题的用于局部使用的组合物(F)中的用于防止太阳紫外线的试剂中,可以提及的是颜料、有机防晒剂和无机防晒剂。
作为用作可以包括在作为本发明主题的用于局部使用的组合物(F)中的用于防止太阳紫外线的试剂的颜料,存在例如二氧化钛、褐色铁氧化物、黄色铁氧化物、黑色铁氧化物或红色铁氧化物、或白色或有色珠光颜料如氧化钛涂覆的云母。
作为用作可以包括在作为本发明主题的用于局部使用的组合物(F)中的用于防止太阳紫外线的试剂的有机防晒剂,存在例如:
-苯甲酸衍生物家族的那些,如对-氨基苯甲酸(PABA),尤其是PABA的单甘油酯、N,N-丙氧基PABA的乙基酯、N,N-二乙氧基PABA的乙基酯、N,N-二甲基PABA的乙基酯、N,N-二甲基PABA的甲基酯、N,N-二甲基PABA的丁基酯;
-邻氨基苯甲酸衍生物家族的那些,如N-乙酰基邻氨基苯甲酸三甲环己酯;
-水杨酸衍生物家族的那些,如水杨酸戊酯、水杨酸三甲环己酯、水杨酸乙基己酯、水杨酸苯酯、水杨酸苄酯、水杨酸对异丙醇苯基酯;
-肉桂酸衍生物家族的那些,如肉桂酸乙基己酯、4-异丙基肉桂酸乙酯、2,5-二异丙基肉桂酸甲酯、对甲氧基肉桂酸丙酯、对甲氧基肉桂酸异丙酯、对甲氧基肉桂酸异戊酯、对甲氧基肉桂酸辛酯(对甲氧基肉桂酸2-乙基己酯)、对甲氧基肉桂酸2-乙氧基乙酯、对甲氧基肉桂酸环己酯、α-氰基-β-苯基肉桂酸乙酯、α-氰基-β-苯基肉桂酸2-乙基己酯、或二(对甲氧基肉桂酸)单(2-乙基己酰基)甘油酯;
-二苯甲酮衍生物家族的那些,如2,4-二羟基二苯甲酮、2,2’-二羟基-4-甲氧基二苯甲酮、2,2’,4,4’-四羟基二苯甲酮、2-羟基-4-甲氧基二苯甲酮、2-羟基-4-甲氧基-4’-甲基二苯甲酮、2-羟基-4-甲氧基二苯甲酮-5-磺酸酯、4-苯基二苯甲酮、4’-苯基二苯甲酮-2-甲酸2-乙基己酯、2-羟基-4-(正辛氧基)二苯甲酮、4-羟基-3-羧基二苯甲酮;3-(4’-甲基亚苄基)-d,l-樟脑、3-亚苄基-d,l-樟脑、樟脑苯扎铵甲基硫酸酯;尿刊酸、尿刊酸乙酯;
-磺酸衍生物家族的那些,如2-苯基苯并咪唑-5-磺酸及其盐;三嗪衍生物的家族,如羟基苯基三嗪、乙基己氧基羟基苯基-4-甲氧基苯基三嗪、2,4,6-三苯胺基(对-羰基(carbo)-2’-乙基己基-1’-氧基)-1,3,5-三嗪、苯甲酸的4,4-((6-(((1,1-二甲基乙基)氨基)羰基)苯基)氨基)-1,3,5-三嗪-2,4-二基二亚氨基)双-(2-乙基己基)酯、2-苯基-5-甲基苯并噁唑、2,2’-羟基-5-甲基苯基苯并三唑、2-(2’-羟基-5’-叔辛基苯基)苯并三唑、2-(2’-羟基-5’-甲基苯基)苯并三唑;二苯并吖嗪(dibenzazine);二对甲氧苯甲酰基甲烷、4-甲氧基-4”-叔丁基苯甲酰基甲烷;5-(3,3-二甲基-2-降冰片烯)-3-戊-2-酮;2-(4-二乙基氨基-2-羟基苯甲酰基)苯甲酸己酯、2,4-双{[4-(2-乙基己氧基)-2-羟基]苯基}-6-(4-甲氧基苯基)-1,3,5-三嗪、2,4,6-三[4-(2-乙基己氧基羰基)苯胺基]-1,3,5-三嗪、2-乙基己基二甲氧基亚苄基二氧代咪唑烷丙酸酯;二苯基丙烯酸酯衍生物家族,例如2-氰基-3,3-二苯基-2-丙烯酸2-乙基己基酯、或2-氰基-3,3-二苯基-2-丙烯酸乙基酯;
-聚硅氧烷家族的那些,如亚苄基硅氧烷丙二酸酯。
作为用作可以包括在作为本发明的主题的用于局部使用的组合物(F)中的用于防止太阳紫外线的试剂的无机防晒剂,存在例如氧化钛、氧化锌、氧化铈、氧化锆、黄色铁氧化物、红色铁氧化物或黑色铁氧化物、以及氧化铬。这些无机防晒剂可以进行或可以不进行微粉化,可以经历或可以不经历表面处理,并且可以任选地呈水性或油性预分散体的形式。
在可以包括在作为本发明的主题的用于局部使用的组合物(F)中的抗氧化剂之中,可以提及EDTA及其盐、柠檬酸、酒石酸、草酸、BHA(丁基羟基苯甲醚)、BHT(丁基羟基甲苯)、生育酚衍生物如生育酚乙酸酯、抗氧化剂化合物的混合物如Dissolvine GL 47S(INCI名称:谷氨酸二乙酸四钠)。
在可以包括在作为本发明的主题的用于局部使用的组合物(F)中的活性成分之中,可以提及:
-维生素及它们的衍生物、特别是它们的酯类,如视黄醇(维生素A)及其酯(例如棕榈酸视黄酯)、抗坏血酸(维生素C)及其酯、抗坏血酸的糖衍生物(如抗坏血酸基葡萄糖苷)、生育酚(维生素E)及其酯(如生育酚乙酸酯)、维生素B3或B10(烟酰胺及其衍生物);显示舒缓作用的化合物,特别是SepicalmTM S、尿囊素和红没药醇;抗炎剂;显示保湿作用的化合物,如脲、羟基脲、甘油葡萄糖苷、二甘油葡萄糖苷、聚甘油葡萄糖苷、甘油聚葡萄糖苷、二甘油聚葡萄糖苷以及xylityl聚葡萄糖苷(商标名AquaxylTM出售);富含多酚类的植物提取物,如葡萄提取物、松树提取物、葡萄酒提取物或橄榄提取物;显示减肥或解脂作用的化合物,如咖啡因或其衍生物、AdiposlimTM、AdipolessTM或岩藻黄质;N-酰化蛋白质;N-酰化肽如MatrixilTM;N-酰化氨基酸;N-酰化蛋白质的部分水解产物;氨基酸;肽;蛋白质的总水解产物;大豆提取物,例如RaffermineTM;小麦提取物,例如TensineTM或GliadineTM;植物提取物,如富含单宁的植物提取物、富含异黄酮的植物提取物或富含萜烯的植物提取物;淡水藻或海藻的提取物;海洋植物提取物;海洋提取物,通常如珊瑚;精华蜡(essential wax);细菌提取物;神经酰胺;磷脂;显示抗微生物作用或净化作用的化合物,如LipacideTM C8G、LipacideTM UG、SepicontrolTM A5、OctopiroxTM或SensivaTM SC50;显示激励或刺激特性的化合物,如PhysiogenylTM、或泛醇以及其衍生物如SepicapTM MP;抗衰老活性成分,例如SepiliftTM DPHP、LipacideTM PVB、SepivinolTM、SepivitalTM、ManolivaTM、Phyto-AgeTM、TimecodeTM或SurvicodeTM;抗光老化活性成分;保护真皮表皮交界处的完整性的活性成分;增加细胞外基质组分的合成的活性成分,如胶原、弹性蛋白或糖胺聚糖;在化学细胞通信上有利地作用的活性成分,如细胞因子,或在物理细胞通信上有利地作用的活性成分,如整合素;在皮肤上产生“加热”感觉的活性成分,如皮肤微循环激活剂(如烟酸衍生物)或在皮肤上产生“清凉”感觉的产品(如薄荷醇和衍生物);改善皮肤微循环的活性成分,例如静脉张力剂(venotonics);排水活性成分;具有减充血目的的活性成分,如银杏、常春藤、马栗树、竹、花竹柏(ruscus)、金雀花(butcher’s broom)、积雪草、岩藻、迷迭香或柳树的提取物;用于晒黑或致黑皮肤的试剂,例如像二羟基丙酮(DHA),赤藓酮糖,内消旋酒石醛,戊二醛,甘油醛,阿脲(alloxan)、茚三酮,植物提取物,例如像紫檀属和巴非豆(Baphia)属的红木提取物,例如檀香紫檀(Pterocarpus santalinus)、非洲紫檀(Pterocarpus osun)、绍氏紫檀(Pterocarpus soyauxii)、刺猬紫檀(Pterocarpus erinaceus)、印度紫檀(Pterocarpusindicus)或非洲小叶紫檀(Baphia nitida),如在欧洲专利申请EP 0 971 683中描述的那些;以其促进和/或加速人体皮肤的晒黑或致黑的作用和/或以其着色人体皮肤的作用已知的试剂,例如像类胡萝卜素(并且更特别地β-胡萝卜素和γ-胡萝卜素),由Provital公司以商标名Carros Oil(INCI名称:胡萝卜(Daucus carota),向日葵葵花子油)出售的产品,其含有类胡萝卜素、维生素E和维生素K;酪氨酸和/或其衍生物,以其在与暴露于紫外线辐射组合对加速人皮肤的晒黑中的作用已知,例如像由Provital公司以商标名“SunTanAcceleratorTM”出售的产品,其含有酪氨酸和核黄素(维生素B);由Zymo Line公司以商标名“Zymo Tan Complex”出售的酪氨酸和酪氨酸酶的络合物;由Mibelle公司以商标名MelanoBronzeTM(INCI名称:乙酰酪氨酸,西洋牡荆(Monk’s pepper)提取物(Vitex agnus-castus))出售的产品,其含有乙酰酪氨酸;由Unipex公司以商标名Unipertan VEG-24/242/2002(INCI名称:丁二醇和乙酰基酪氨酸和水解的植物蛋白质和三磷酸腺苷)出售的产品;由Sederma公司以商标名“Try-ExcellTM”(INCI名称:油酰基酪氨酸和丝瓜提取液(种子油和油酸)出售的产品,其含有西葫芦种子(或丝瓜油)的提取物;由Alban Muller公司以商标名“ActibronzeTM”(INCI名称:水解的小麦蛋白质和乙酰酪氨酸和葡萄糖酸铜)出售的产品;由Synerga公司以商标名TyrostanTM(INCI名称:己酰基酪氨酸钾)出售的产品;由Synerga公司以商标名Tyrosinol(INCI名称:脱水山梨糖醇异硬脂酸酯、油酸甘油酯、己酰基酪氨酸)出售的产品;由Alban Muller公司以商标名InstaBronzeTM(INCI名称:二羟基丙酮和乙酰基酪氨酸和葡萄糖酸铜)出售的产品;由爱西美公司(Exsymol)以商标名Tyrosilane(INCI名称:甲基硅烷醇和乙酰酪氨酸)出售的产品;以其激活黑素生成的作用而已知的肽,例如像由Infinitec Activos公司以商标名Bronzing SF肽粉(INCI名称:葡聚糖和八肽-5)出售的产品,以商标名Melitane(INCI名称:甘油和水和葡聚糖和乙酰六肽-1)出售的产品,其包含以α-MSH激动剂作用而已知的乙酰六肽-1,由Lipotec公司以商标名Melatimes SolutionsTM(INCI名称:丁二醇,棕榈酰三肽-40)出售的产品,糖和糖衍生物,例如像由Provital公司以商标名TanositolTM(INCI名称:肌醇)出售的产品,由Codif International公司以商标名ThalitanTM(或PhycosaccharideTMAG)出售的产品(INCI名称:水和水解藻酸盐(掌状海带(Laminaria digitata))和硫酸镁和硫酸锰),其含有海洋来源的低聚糖(与镁和锰离子螯合的古洛糖醛酸和甘露糖醛酸),由Alban Muller公司以商标名MelactivaTM(INCI名称:麦芽糊精,刺毛黧豆(Mucuna pruriens)种子提取物)出售的产品,富含类黄酮的化合物,例如由茜莱博公司(Silab)以商标名“Biotanning”(INCI名称:水解甜橙(citrus Aurantiumdulcis)果实提取物)出售并已知富含柠檬类黄酮(橙皮苷(hesperidin)类)的产品。
在可以包括在作为本发明的主题的用于局部使用的组合物(F)中的质地剂之中,可以提及月桂酰赖氨酸(由味之素公司(Ajinomoto)以名称AminohopeTM LL出售),辛烯基琥珀酸淀粉酯(由国民淀粉公司(National Starch)以名称DryfloTM出售),肉豆蔻基聚葡萄糖苷(由赛比克公司(SEPPIC)以名称MontanovTM 14出售),纤维素纤维,棉纤维或壳聚糖纤维。
在可以包括在作为本发明的主题的用于局部使用的组合物(F)中的芳香或调味物质之中,可以提及:
-植物不同部分的提取物:花、叶、茎或木、树皮或木苔藓、果实或种子、根,
-花如玫瑰、茉莉、晚香玉、黄兰花、鸡蛋花、依兰花、莲花、含羞草花、康乃馨花、桂花、金合欢花、甜橙花、苦橙花或橙花、水仙花、薰衣草、栀子的提取物,
-叶、苔藓、树皮、树脂或芽如黑加仑芽、橡木苔、山毛榉苔藓、地衣、金合欢叶、罗勒叶、缬草叶、龙胆叶、紫罗兰叶、天竺葵叶、劳丹脂叶、迷迭香、广藿香叶、马鞭草叶、肉桂皮、秦皮、桂皮、卡黎皮、檀香木、雪松木、蔷薇木、沉香木、桦树皮、愈创木、秘鲁香脂、吐鲁香脂、安息香树脂、没药、劳丹脂树脂、榄香树脂、乳香脂、红没药、印度没药、松树或云杉或冷杉的针叶和树枝的提取物,
-草药或草如龙蒿、柠檬草、鼠尾草、百里香的提取物,
-果实或种子提取物如零陵香豆、香草荚、小豆蔻、芫荽、八角茴香、苦杏仁、小茴香、丁香、杜松果、柑橘类水果如柠檬、橙子(包括甜柠檬和佛手柑)、柑橘,
-根如当归、芹菜、小豆蔻、鸢尾花、白菖蒲、仙人掌、或香根草的根的提取物,
-芳烃提取物、净油、醇化物和精油。
术语“精油”理解为意指根据化妆品法规从植物学定义的植物原料获得的通常具有复杂组成的芳香产品。标准ISO 9235中描述了用于获得精油的方法,并且这些精油也许可能经历了适当的后续处理,如已脱萜、脱倍半萜、或精馏。
作为可以与做为本发明的主题的用于局部使用的组合物(F)组合的精油,可以提及例如蓍草精油、菖蒲(Acorus calamus)精油、大蒜精油、香旱芹精油、阿米香树精油、莳萝精油、茴香芹精油、当归精油、茶树精油、罗勒精油、Bay Saint Thomas精油、安息香精油、佛手柑精油、愈创木精油、芳樟精油、花梨木精油、檀香精油、暹罗木精油、黑桦木精油、洋甘菊精油、樟树精油、肉桂精油、小豆蔻精油、胡萝卜精油、葛缕子精油、雪松精油、芹菜精油、海茴香精油、岩蔷薇精油、柠檬精油、香茅精油、克莱门柑橘精油、泰国柠檬精油、苦配巴精油、芫荽精油、柳杉精油、孜然精油、姜黄精油、丝柏精油、乳香精油、云杉精油、龙蒿精油、茴香精油、芳枸叶精油、白松香精油、冬青精油、杜松精油、天竺葵精油、生姜精油、丁香或丁香叶精油、永久花精油、牛膝草精油、iary精油、土木香精油、卡塔芙精油、阿密茴精油、昆士亚精油、薰衣草精油、杂薰衣草精油、柑橘精油、绿花白千层精油、薄荷精油、橙子精油、葡萄柚精油、迷迭香精油、百里香精油、依兰依兰精油、罗文莎叶精油、鼠尾草精油、红檀香精油、柠檬草精油、玫瑰草精油、圣约翰草精油(St.John’s wort essential oil)、茉莉精油、洋甘菊精油、香蜂草精油、松树精油、生姜精油、欧芹精油、艾草精油、火麻精油(hemp essentialoil)、啤酒花精油、或者野百里香精油。
在可以与作为本发明的主题的用于局部使用的组合物(F)组合的动物“芳香或调味物质”中,可以提及例如麝香、海狸香、麝猫香、龙涎香、蜂蜡净油和蹄兔香。这些物质还可以通过合成重构。
在可以与作为本发明的主题的用于局部使用的组合物(F)组合的合成“芳香或调味物质”中,可以提及例如:
a)萜烯烃(单萜烯和倍半萜烯),如月桂烯(α-月桂烯或β-月桂烯,和α-月桂烯)、柠檬烯、α-蒎烯、β-蒎烯、莰烯、杜松烯、柏木烯、法呢烯、石竹烯、母菊兰烯、1,1-二甲氧基-2,2,5-三甲基-4-己烯、姜黄烯、海茴香烯、雪松烯、柠檬烯、对伞花烃、玫瑰醚、由芬美意公司(Firmenich)以名称Ambrox出售的四降半日花烷氧化物(tetranorlabdane oxide)、松油烯和萜品油烯、岩兰烯,
b)酯类如乙酸苄酯、乙酸冰片酯、乙酸香茅酯、乙酸柏木酯、乙酸二氢月桂烯酯、乙酸二甲基苄基原酯、乙酸乙酯、乙酸法呢酯、乙酸葑酯、乙酸己酯、乙酸香叶酯、乙酸异丁酯、乙酸异壬酯、乙酸异戊酯、乙酸异冰片酯、乙酸异胡薄荷酯、乙酸芳樟酯、乙酸薄荷酯、乙酸甲基苯基原酯、乙酸橙花酯、乙酸壬酯、乙酸邻叔丁基环己酯、乙酸苯乙酯、乙酸对叔丁基环己酯、乙酸苯乙酯、乙酸异戊二烯酯、乙酸苏合香酯、乙酸萜烯酯、乙酸4-叔丁基环己酯、乙酸香根酯、邻氨基苯甲酸甲酯、苯甲酸苄酯、苯甲酸异丁酯、苯甲酸芳樟酯、香豆素、丁酸乙酯(ethyl butanoate)、丁酸苄酯(benzyl butanoate)、丁酸异戊酯(isoamyl butanoate)、丁酸苄酯(benzyl butyrate)、丁酸乙酯(ethyl butyrate)、丁酸乙酯(ethyl butyrate)、丁酸异戊酯(isoamyl butyrate)、丁酸芳樟酯、肉桂酸丁酯、己酸烯丙酯、肉桂酸乙酯、甲酸苄酯、甲酸香茅酯、希蒂莺(二氢茉莉酮酸甲酯)、甲酸香叶酯、甲酸甲酯、甘氨酸乙基甲基苯酯、格蓬酯、庚酸烯丙酯、异丁酸苯氧基乙酯、异丁酸顺式-3-己烯酯、甲基丙烯酸异戊酯、萘甲酸乙酯、新戊酸己酯、丙酸戊酯、丙酸烷基环己酯、丙酸烯丙基环己酯、丙酸芳樟酯、丙酸苏合香酯、丙酸香茅酯、水杨酸甲酯、水杨酸苄酯、水杨酸乙酯、惕各酸己酯,
c)醇类和酚类,如苄醇、α-萜品醇、茴香脑、胡萝卜醇、佳味酚、草蒿脑、桉树脑、肉桂醇、香茅醇、对甲酚、枯基醇、3,7-二甲基-1-辛醇、二甲基苄基甲醇、葑醇、桉油精、法尼醇、丁香酚、异壬醇、异丁香酚、愈创木酚、香叶醇、蓝桉醇、芳樟醇、薄荷醇、二氢月桂烯醇、橙花叔醇、橙花醇、苯乙醇、黄樟脑、异黄樟脑、植醇、异植醇、萜品醇、四氢芳樟醇、四氢月桂烯醇、百里酚、岩兰草醇、甲基癸烯醇(undecavertol),
d)醛类,如苯乙醛、水杨醛、茴香醛、辛醛(caprylaldehyde)、肉桂醛、己基肉桂醛、波洁红醛(bourgeonal)、柠檬醛(橙花醛)、香茅醛、羟基香茅醛、香茅氧基乙醛、仙客来醛、枯茗醛、四氮杂环十五烷、2,4-二甲基-3-环己烯-1-甲醛(女贞醛)、十二醛、癸醛(decylaldehyde)、乙醛、辛醛(octanal)、癸醛(decanal)、香叶醛、新洋茉莉醛、月桂醛、内酯如γ-十一内酯、铃兰醛、甲基-正壬基乙醛、甲基辛基乙醛、十一醛、水杨醛、香草醛,
e)酮类,如苄基丙酮、西瓜酮(7-甲基-2H-苯并-1,5-二氧杂卓-3(4H)-酮)、香芹酮、樟脑、灵猫酮、大马酮、大马烯酮、乙基戊基酮、乙基己基酮、香叶基丙酮、茉莉酮、鸢尾酮、麦芽酚(3-羟基-2-甲基-4H-吡喃-4-酮)、乙基麦芽酚、薄荷酮、异薄荷酮、麝香酮、甲基庚烯酮、紫罗兰酮类如甲基紫罗兰酮、4-甲基苯乙酮、甲基戊基酮、甲基庚基酮、甲基已基酮、α-异甲基紫罗兰酮、和由国际香料公司(IFF)以名称Vertofix出售的甲基柏木酮,
f)醚类如茴香脑、苄基乙基醚、柏木甲醚、对甲酚甲醚,
g)衍生自不同硝基化合物、葵子麝香、麝香酮、二甲苯麝香、大环麝香的人造麝香,
h)腈类,如三甲基-3,5,7-辛烷(烯)腈及其α-取代衍生物、香茅腈、柑桔腈、香叶腈。
根据另一方面,本发明的主题是如上定义的交联的阴离子聚电解质类型的聚合物(P)用于改善如上所述的用于局部使用的化妆品配制品(F)的冲击强度的用途。
根据另一方面,本发明的主题是一种用于化妆人体皮肤的方法,该方法包括向所述人体或动物皮肤施用如上定义的用于局部使用的组合物(F)的至少一个步骤。
根据另一方面,本发明的主题是根据本发明的用于局部使用的组合物(F),该组合物包含有效量的至少一种有机防晒剂和/或至少一种无机防晒剂,用于保护人体皮肤免受太阳紫外线对所述人体皮肤的不美观影响。
术语“太阳紫外线对所述人体皮肤的不美观影响”表示不希望的过度着色,如皮肤上的红色斑块、可能可以导致皮肤起皱的皮肤可塑性变化、出现皱纹和/或明显的细纹,处于表面脱屑,通常称为“皮肤脱皮”,对应于由于皮肤长时间暴露于太阳紫外线而导致死皮脱落增加。
可使用手指或涂抹器例如像刷子或海绵进行所述将用于局部使用的组合物(F)施用于皮肤的步骤。
以下实例阐明本发明,然而不限制本发明。
实例1:
1.1.用三羟甲基丙烷三丙烯酸酯(TMPTA)交联的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸铵、N,N-二甲基丙烯酰胺和四乙氧基化的甲基丙烯酸月桂酯[AMPS/DMAM/LMA(4EO)77.4/19.2/3.4摩尔]的三元共聚物的制备。[根据本发明的实例]
将592g含有在叔丁醇/水混合物(按体积计97.5/2.5)中的按质量计15%的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸铵的水溶液、10.1g的N,N-二甲基丙烯酰胺、4.2g的四乙氧基化的甲基丙烯酸月桂酯和0.75g的三羟甲基丙烷三丙烯酸酯装载到保持在25℃在搅拌下的反应器中。
在足够时间以实现溶液的良好均化之后,将其通过用加热至70℃的氮气鼓泡而脱氧。然后添加0.42g的过氧化二月桂酰并且然后将反应介质在70℃保持约60分钟并且然后在80℃下保持2小时。
冷却后,将在聚合期间形成的粉末过滤掉并干燥以得到所希望的产物,以下称为:聚电解质1
1.2用三羟甲基丙烷三丙烯酸酯交联的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸铵、丙烯酸(2-羟乙基)酯、甲基丙烯酸硬脂酯和甲基丙烯酸月桂酯(ATBS/HEA/SMA/LAUMA:88.1/9.9/1.0/1.0;聚电解质2)的交联的聚电解质。
将以下装载到保持在25℃在搅拌下的并含有245g叔丁醇的反应器中:
-33.8g的2-丙烯酰胺基-2-甲基丙磺酸(ATBS);
-12.9g的碳酸氢铵;
-2.12g的丙烯酸(2-羟乙基)酯(HEA);
-0.62g的甲基丙烯酸硬脂酯(SMA);
-0.48g的甲基丙烯酸月桂酯(LAUMA);
-0.54g的三羟甲基丙烷三丙烯酸酯(TMPTA)。
在足够时间以实现溶液的良好均化之后,将其通过用氮气鼓泡而脱氧,并然后使介质温度达到70℃。当达到所希望的温度时,添加0.50g的过氧化二月桂酰。聚合立即开始。然后将反应介质在该温度下保持大约60分钟,并然后将混合物加热至80℃。在冷却之前保持该温度持续2小时。将在聚合期间形成的粉末过滤掉并干燥以获得聚电解质2。
1.3.用三羟甲基丙烷三丙烯酸酯(TMPTA)交联的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸铵、丙烯酸2-羟乙酯和四乙氧基化的甲基丙烯酸月桂酯[AMPS/HEA/LMA(4EO)77.4/19.2/3.4摩尔]的三元共聚物的制备。
在采用以上实例1.1中描述的方法的操作条件的同时,在保持在25℃下在搅拌下的反应器中装入引入77.4摩尔当量的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸铵所需的按质量计的量的含有在叔丁醇/水混合物(按体积计97.5/2.5)中的按质量计15%的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸铵的水溶液,引入19.2摩尔当量的丙烯酸2-羟乙酯所需的按质量计的量的丙烯酸2-羟乙酯,引入3.4摩尔当量的四乙氧基化的甲基丙烯酸月桂酯所需的按质量计的量的四乙氧基化的甲基丙烯酸月桂酯,以及获得与实例1.1中相同摩尔比例的三羟甲基丙烷三丙烯酸酯所需的按质量计的量的三羟甲基丙烷三丙烯酸酯。
在足够时间以实现溶液的良好均化之后,将其通过用加热至70℃的氮气鼓泡而脱氧。然后添加0.42g的过氧化二月桂酰并且然后将反应介质在70℃保持约60分钟并且然后在80℃下保持2小时。
冷却后,将在聚合期间形成的粉末过滤掉并干燥以得到所希望的产物,以下称为:聚电解质3。
1.4.制备用亚甲基双(丙烯酰胺)(MBA)交联的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸铵和丙烯酸2-羟乙酯[AMPS/HEA 90/10摩尔]的共聚物的制备。
在搅拌下,将以下各项置于烧杯中:
-608.8g的含有50%2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸钠盐的商业溶液,
-72.6g的丙烯酸(2-羟乙基)酯,
-0.18g的二亚乙基三胺五乙酸钠,和
-0.121g的亚甲基双(丙烯酰胺),
-通过添加0.7g的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸将上面描述的水相的pH调节至3.5。
平行地,通过将以下依次引入搅拌烧杯中来制备有机相:
-220g的Isopar M,
-25g的Montane 70VG(由赛比克公司出售的用20摩尔环氧乙烷乙氧基化的脱水山梨醇油酸酯)和
-0.2g的偶氮双(异丁腈)。
将水相逐渐引入有机相中,并且然后使用由IKA公司出售的Ultra-Turrax使其经受强烈机械搅拌。
然后将获得的乳液转移到聚合反应器中。使乳液经受显著的氮气鼓泡以便除去氧并冷却至约5℃-6℃。
然后引入10g在异十六烷中含有按重量计1.1%的氢过氧化枯烯活性物质的溶液。在足够时间进行溶液的良好均化之后,在约25分钟内引入25g的焦亚硫酸钠水溶液(0.2%溶液)。在此引入期间,允许聚合反应器中的温度升至最终聚合温度,并然后将反应介质在此温度下保持大约90分钟。
然后将所得混合物冷却至约35℃的温度以获得乳液,然后借助于NiroTM型装置将其雾化,并获得呈粉末形式的聚电解质4。
在上述实例1.4中,具有式(1)单体不参与聚合反应,从而具有交联的阴离子聚电解质(聚电解质4),其旨在用于比较与在交联的阴离子聚电解质的聚合物骨架中具有式(1)单体的存在相关的作用。
实例2:
A-根据本发明的包含聚电解质1至4的压实组合物和对比配制品的制备。
将待测试的有色颜料、填充剂(滑石粉)和交联的阴离子聚电解质引入ThermomixTM3300型号的Vorwerk牌刀磨机。然后在25℃的温度下、在7700转/分钟的搅拌速度下,使粉末混合物经受连续的研磨操作,3次30秒。在每次研磨操作之间刮转筒壁,以便在研磨步骤期间夹带所有粉末。
然后使粘合剂分布于由此在粉碎机转筒中获得的粉末混合物中,并然后使这种新混合物经受研磨操作,3次30秒,在每次研磨之间有效地刮转筒壁。
将最佳量的11g这种混合物引入直径3cm的金属罐中,并将“佛手柑”型织物(100%聚酰胺)放置在罐的表面上。
然后将此罐放置在手动“压实机”中,即用于通过施加确定的压力来压实罐中存在的粉末的装置。
然后在25℃的温度下向罐施用130巴的压力持续1秒的时间段。
得到了如下表1和表2中所描述的根据本发明的配制品(F1)、(F2)、(F3)、(F4)以及对比配制品(F5)、(F6)、(F’1)和(F’2)。
[表1]
[表2]
B-与现有技术的那些相比,根据本发明的压实配制品的特性和特征的证明。
然后如下评估预先制备的配制品(F1)至(F6)以及对比配制品(F’1)和(F’2):
-根据“跌落测试”方法测量其冲击强度,
-评估在环境温度(25℃)下对皮肤的转移,
-评估在50℃潮湿大气中储存后对皮肤的转移。
根据用于配制品(F1)至(F6)和配制品(F’1)和(F’2)的“跌落测试”方法评估冲击
强度的实验方案
·原理:确定待测试的压实配制品表面开始出现裂纹和/或破碎的连续跌落次数。
·设备:金属罐,直径3cm,含有待测试的压实配制品,用于跌落的管状导承
·程序:根据上述程序制备待测试的配制品,并在直径3cm的罐中获得。每个罐放置在距地面20cm的高度,并从所述高度沿管状导承释放x次。在每次跌落之后,实验者观察存在于罐中的配制品的表面,并根据情况注明“表面上不存在裂纹或破碎”或“表面上存在裂纹或破碎”。然后实验者确定第一次观察到“表面上存在裂纹或破碎”所需的连续跌落次数。对每种配制品重复测试3次。
用于评估在25℃和50℃下配制品(F1)至(F6)和配制品(F’1)对皮肤的转移品质的
实验方案
·原理:通过估计将手指划过罐之后收集到的量的充分性,来定性在25℃和50℃下待测试的压实配制品向实验者手指的转移。
·设备:金属罐,直径3cm,含有待测试的压实配制品
·程序:根据上述程序制备待测试的配制品,并在直径3cm的罐中获得。在每次测试之前,实验者用肥皂洗手并擦干手以去除因冲洗产生的水分。然后实验者将其手指划过包含待测试的配制品的罐的表面,以便取一些。然后实验者使用以下标准确定收集的量的充足性:“吸收不充足”、“吸收一般”和“吸收良好”。
·测量条件:配制品在25℃和环境湿度以及在50℃潮湿条件下储存7天后进行测试:对于这些测量,将罐放置在置于在50℃的烘箱的封闭的腔室中的水床上方持续7天。在第1天、第3天和第7天测量。
这些评价的结果在下表3和4中示出。
[表3]
[表4]
评论和结论
在以下情况下,认为结果是令人满意的:
-实验者没有观察到“表面上存在裂纹或破碎”的连续跌落次数大于或等于5,并且
-判定在25℃的吸收品质为“吸收良好”
-判定在50℃的吸收品质为“吸收良好”
分别包含按质量计0.5%的聚电解质1、聚电解质2和聚电解质3的配制品(F1)、(F2)和(F3)显示出所希望的冲击强度(在观察到裂纹之前的跌落次数分别为8、7和5)并判定在25℃和50℃下的吸收品质为“吸收良好”。相比之下,包含基于用亚甲基双(丙烯酰胺)交联的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸的钠盐和丙烯酸2-羟乙酯的共聚物,但不包含如上定义的具有式(I)单体的配制品(F’1),展现出差的冲击强度,因为只进行单次跌落,压实配制品(F’1)的表面上就出现裂纹。
根据50℃的测试,包含组合物(C1)中的按质量计的比例大于0.7%的交联的阴离子聚电解质(P)的对比配制品(F5)和(F6)的特征在于在皮肤上的吸收较差。
对比配制品(F’2),其特征在于不存在交联的阴离子聚电解质型聚合物(P),显示出未改善的冲击强度。
Claims (16)
1.一种呈粉末形式的粉状组合物(C1),该粉状组合物每100%其质量包含:
i)按质量计从84.3%至95.8%的至少一种填充剂(FA)
ii)按质量计从4%至15%的至少一种有色颜料(CP)
-iii)按质量计从0.2%至0.7%的至少一种交联的阴离子聚电解质类型的聚合物(P),其每100mol%包含从65mol%至95mol%的衍生自部分或完全成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸的单体单元,从4.8mol%至25mol%的衍生自至少一种选自由以下组成的组的要素的中性单体的单体单元:丙烯酸2-羟乙酯、甲基丙烯酸2-羟乙酯、N,N-二烷基丙烯酰胺——其中每个烷基包含一与四个之间的碳原子,以及从0.1mol%至5mol%的衍生自至少一种具有式(I)的单体的单体单元:
[化学式1]
其中R表示直链或支链的包含从八至二十个碳原子的烷基,并且n表示大于或等于零且小于或等于二十的数,以及从0.1mol%至5mol%的衍生自至少一种二烯属或多烯属交联单体的单体单元。
2.如权利要求1所述的粉状组合物(C1),其特征在于,在该交联的阴离子聚电解质类型的聚合物(P)中,所述中性单体选自由丙烯酸2-羟乙酯或N,N-二甲基丙烯酰胺组成的组的要素。
3.如权利要求1和2中任一项所述的粉状组合物(C1),其特征在于,在该交联的阴离子聚电解质类型的聚合物(P)中,所述具有式(I)的单体选自由以下组成的组的要素:具有式(I1)的四乙氧基化的甲基丙烯酸月桂酯,其对应于其中R表示正十二烷基并且其中n等于四的式(I),具有式(I2)的甲基丙烯酸月桂酯,其对应于其中R表示正十二烷基并且其中n等于零的式(I),具有式(I’2)的甲基丙烯酸异癸酯其对应于其中R表示异十二烷基并且其中n等于零的式(I),以及具有式(I3)的甲基丙烯酸硬脂酯,其对应于其中R表示正十八烷基并且其中n等于零的式(I)。
4.如权利要求1至3之一所述的粉状组合物(C1),其特征在于,在该交联的阴离子聚电解质类型的聚合物(P)中,该二烯属或多烯属交联单体选自乙二醇二甲基丙烯酸酯、四烯丙氧基乙烷、乙二醇二丙烯酸酯、二烯丙基脲、三烯丙基胺、三羟甲基丙烷三丙烯酸酯、亚甲基双(丙烯酰胺),或这些化合物的混合物。
5.如权利要求1至4之一所述的粉状组合物(C1),其特征在于,所述交联的阴离子聚电解质类型的聚合物(P)是用三羟甲基丙烷三丙烯酸酯交联的以铵盐形式部分或完全成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸、N,N-二甲基丙烯酰胺以及具有式(I1)的四乙氧基化的甲基丙烯酸月桂酯的聚合物。
6.如权利要求5所述的粉状组合物(C1),其特征在于,所述交联的阴离子聚电解质类型的聚合物(P)每100mol%包含:
-从65mol%至95mol%的衍生自以铵盐形式成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸的单体单元;
-从4.8mol%至25mol%的衍生自N,N-二甲基丙烯酰胺的单体单元,
-从0.1mol%至5mol%的衍生自具有式(I1)的四乙氧基化的甲基丙烯酸月桂酯的单体单元,
-从0.1mol%至5mol%的衍生自三羟甲基丙烷三丙烯酸酯的单体单元。
7.如权利要求1至4之一或之中任一项所述的粉状组合物(C1),其特征在于,所述交联的阴离子聚电解质类型的聚合物(P)是以钠盐形式部分或完全成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸,丙烯酸2-羟乙酯,以大于或等于1/10且小于或等于10/1的(I2)/(I3)或(I’2)/(I3)的摩尔比的具有式(I2)的甲基丙烯酸月桂酯或具有式(I’2)的甲基丙烯酸异癸酯的和具有式(I3)的甲基丙烯酸硬脂酯的并用三羟甲基丙烷三丙烯酸酯交联的聚合物。
8.如权利要求7所述的粉状组合物(C1),其特征在于,所述交联的阴离子聚电解质类型的聚合物(P)每100mol%包含:
-从70mol%至95mol%的衍生自以钠盐形式成盐的2-甲基-2-[(1-氧代-2-丙烯基)氨基]-1-丙磺酸的单体单元;
-从4.8mol%至20mol%的衍生自丙烯酸2-羟乙酯的单体单元,
-从0.1mol%至5mol%的衍生自以大于或等于1/6且小于或等于6/1的(I2)/(I3)或(I’2)/(I3)的摩尔比的具有式(I2)的甲基丙烯酸月桂酯或具有式(I’2)的甲基丙烯酸异癸酯和衍生自具有式(I3)的甲基丙烯酸硬脂酯的单体单元,
-从0.1mol%至5mol%的三羟甲基丙烷三丙烯酸酯。
9.如权利要求1至8之一或之中任一项所述的粉状组合物(C1),其特征在于,该填充剂(FA)选自由以下组成的组的要素:无机层状类型的填料、有机层状类型的填料、无机球形类型的填料和有机球形类型的填料。
10.如权利要求1至9之一或之中任一项所述的粉状组合物(C1),其特征在于,该有色颜料(CP)选自由以下组成的组的要素:无机颜料、有机颜料和珠光颜料。
11.如权利要求1至10之一或之中任一项所述的粉状组合物(C1),其特征在于,该粉状组合物每100%其质量包含按质量计小于或等于2%的按质量计的含量的水。
12.一种用于局部使用的组合物(F),该组合物每100%其质量包含:
i)按质量计从90%至97%的至少一种如权利要求1至11之一或之中任一项所述的粉状组合物(C1)
ii)按质量计从3%至10%的至少一种在20℃下为液体的脂肪粘合剂(BA)。
13.如权利要求12所述的用于局部使用的组合物(F),其特征在于,该粘合剂(BA)选自由以下组成的组的要素:蓖麻油、辛基十二烷醇、聚二甲基硅氧烷、鲸蜡硬脂醇乙基己酸酯以及肉豆蔻酸异丙酯。
14.如权利要求1至8之一或之中任一项所述的交联的阴离子聚电解质类型的聚合物(P)用于改善用于局部使用的包含至少一种粘合剂(BA)的压实化妆品配制品的冲击强度的用途。
15.如权利要求12和13中任一项所述的用于局部使用的组合物(F),该组合物包含有效量的至少一种有机防晒剂和/或至少一种无机防晒剂,其用于保护人体皮肤免受太阳紫外线对所述人体皮肤的不美观影响。
16.一种用于化妆人体皮肤的方法,其特征在于,该方法包括向所述人体皮肤施用如权利要求12和13中之一或之中任一项所述的用于局部使用的组合物(F)的至少一个步骤。
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PCT/FR2020/051313 WO2021019151A1 (fr) | 2019-07-31 | 2020-07-21 | Composition cosmétique sous la forme d'une poudre compacte, résistante aux chocs |
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CN102325520A (zh) * | 2009-02-19 | 2012-01-18 | 化工产品开发公司Seppic | 粉状的烷基聚糖苷乳化组合物、其用于制备化妆品乳液的用途及其制备方法 |
FR2980108A1 (fr) * | 2011-09-21 | 2013-03-22 | Oreal | Composition cosmetique solide sous forme de poudre compacte |
US20160167040A1 (en) * | 2013-07-24 | 2016-06-16 | Societe D'exploitation De Produits Pour Les Industries Chimiques Seppic | Novel powder polymer, method for the preparation thereof, and use as a thickener |
CN107530271A (zh) * | 2015-04-20 | 2018-01-02 | 化工产品开发公司Seppic | 以泡沫形式提供的新颖的化妆品乳液、其获得方法及其化妆用途 |
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US4557581A (en) | 1984-08-03 | 1985-12-10 | Xerox Corporation | Full-frame short focal length imaging system |
FR2688134B1 (fr) | 1992-03-05 | 1994-04-29 | Oreal | Composition cosmetique sous forme de poudre contenant un liant gras silicone. |
FR2727312B1 (fr) | 1994-11-24 | 1997-05-23 | Oreal | Composition cosmetique sous forme de poudre compacte et procede de preparation |
FR2761595B1 (fr) | 1997-04-04 | 1999-09-17 | Oreal | Compositions comprenant des santalines, santarubines pour la coloration artificielle de la peau et utilisations |
US20050186235A1 (en) | 2004-01-27 | 2005-08-25 | Guenaelle Martin | Compact powder cosmetic compositions with a solid fatty phase |
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CN102325520A (zh) * | 2009-02-19 | 2012-01-18 | 化工产品开发公司Seppic | 粉状的烷基聚糖苷乳化组合物、其用于制备化妆品乳液的用途及其制备方法 |
FR2980108A1 (fr) * | 2011-09-21 | 2013-03-22 | Oreal | Composition cosmetique solide sous forme de poudre compacte |
US20160167040A1 (en) * | 2013-07-24 | 2016-06-16 | Societe D'exploitation De Produits Pour Les Industries Chimiques Seppic | Novel powder polymer, method for the preparation thereof, and use as a thickener |
CN107530271A (zh) * | 2015-04-20 | 2018-01-02 | 化工产品开发公司Seppic | 以泡沫形式提供的新颖的化妆品乳液、其获得方法及其化妆用途 |
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EP4003271A1 (fr) | 2022-06-01 |
FR3099368B1 (fr) | 2022-08-19 |
US20220257475A1 (en) | 2022-08-18 |
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