CN1984636A - 包含二糖、二酸和铵离子源的头发处理组合物 - Google Patents
包含二糖、二酸和铵离子源的头发处理组合物 Download PDFInfo
- Publication number
- CN1984636A CN1984636A CNA2005800106556A CN200580010655A CN1984636A CN 1984636 A CN1984636 A CN 1984636A CN A2005800106556 A CNA2005800106556 A CN A2005800106556A CN 200580010655 A CN200580010655 A CN 200580010655A CN 1984636 A CN1984636 A CN 1984636A
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- China
- Prior art keywords
- hair
- acid
- treatment composition
- compositions
- ammonium
- Prior art date
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- Granted
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- 239000000203 mixture Substances 0.000 title claims abstract description 105
- 238000011282 treatment Methods 0.000 title claims abstract description 27
- 150000002016 disaccharides Chemical class 0.000 title claims abstract description 17
- -1 ammonium ions Chemical class 0.000 title abstract description 61
- 239000002253 acid Substances 0.000 title abstract description 10
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 29
- HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 claims description 19
- HDTRYLNUVZCQOY-WSWWMNSNSA-N Trehalose Natural products O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-WSWWMNSNSA-N 0.000 claims description 19
- HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 claims description 18
- 239000004094 surface-active agent Substances 0.000 claims description 18
- 239000001361 adipic acid Substances 0.000 claims description 15
- 235000011037 adipic acid Nutrition 0.000 claims description 15
- 239000001099 ammonium carbonate Substances 0.000 claims description 14
- 235000012501 ammonium carbonate Nutrition 0.000 claims description 14
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims description 13
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 229940116226 behenic acid Drugs 0.000 description 4
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- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- UZBQIPPOMKBLAS-UHFFFAOYSA-N diethylazanide Chemical compound CC[N-]CC UZBQIPPOMKBLAS-UHFFFAOYSA-N 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- LWIGVRDDANOFTD-UHFFFAOYSA-N hydroxy(dimethyl)silane Chemical compound C[SiH](C)O LWIGVRDDANOFTD-UHFFFAOYSA-N 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 239000004530 micro-emulsion Substances 0.000 description 4
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- 150000003839 salts Chemical class 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
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- 235000011152 sodium sulphate Nutrition 0.000 description 4
- 125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
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- 239000002888 zwitterionic surfactant Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
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- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical class [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 3
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Abstract
本发明提供了一种头发处理组合物,其包含:i)二糖;ii)二酸,和iii)铵离子源。
Description
发明领域
本发明涉及头发处理组合物。更具体而言,本发明涉及包含活性物质特定组合的头发处理组合物。该组合物特别适合施用于头发上以增加头发的易处理性(managability)和湿度控制。
背景和现有技术
消费者需要能够使他们的头发易处理;即,当头发定型后,需要保持该发型很长一段时间,并且需要保持在有害环境条件范围下例如高湿度下。
WO 97/14401(Kao Corporation)公开了在皮肤和头发护理组合物中的宽范围的有机酸。
在WO 01/68040(L′Oreal)中公开了使用糖和植物提取物来保护角蛋白组织。在WO 01/01948中公开了海藻糖已用于提高皮肤的弹性和/或预防衰老。
在共同未决的申请WO 04/054525(Unilever)和WO 04/054526中描述了包含海藻糖的组合物。
现在,本发明已发现包含糖类、酸类和盐类的某些特定组合的组合物可提高头发的易处理性(manageability)。
发明描述
一方面,本发明提供包含占总组合物的0.05至8wt%的i)二糖;ii)铵离子源,和iii)二酸的头发处理组合物。
本发明的另一方面为上述组合物用于定型头发、使头发光滑、使头发整齐(aligning hair)和防止头发损伤的应用。
本发明还涉及通过给头发施用上述组合物的处理头发的方法。
本发明进一步地涉及制备上述的头发处理组合物的方法,其包含将二酸加入到碳酸盐离子源中的步骤。
详细描述
二糖
本发明包含作为本发明必要成分的二糖,优选地,所述二糖包含戊糖或己糖,更优选地,所述二糖包含两个己糖单元。
二糖可以是还原性糖或非还原性糖。优选非还原性糖。
优选糖的D㈩形式。特别优选的是海藻糖或纤维素二糖或其混合物。海藻糖为最优选的二糖。
在总制剂中存在的二糖含量为总组合物的0.05wt%至8wt%,优选为0.1至5wt%,更优选为0.2wt%至3wt%,最优选为0.5wt%至2wt%。
碳酸铵
组合物包含铵离子源,优选的铵离子源为碳酸铵。
碳酸铵优选存在的含量为起自总组合物的0.01wt%,更优选为起自0.05wt%。碳酸铵的最大含量优选为小于10wt%,更优选小于5wt%,最优选小于1wt%。进一步优选的是,碳酸铵的含量为总组合物的0.01至2.0wt%。
二酸
本发明的组合物中存在二酸,特别适宜的二酸具有下式:
HOOC-(CH2)n-COOH
其中n为2至8的整数,更优选其中n等于2或4(分别为琥珀酸和己二酸)。
在总制剂中最佳使用的二酸含量为总组合物的0.01wt%至5wt%,更优选地含量为0.1wt%至2wt%。
二酸与二糖的重量比为1∶10至20∶1,更优选为1∶5至5∶1。
而且,最佳使用的酸量为二酸:二糖摩尔比为0.1∶1至10∶1,优选为0.1∶1至2∶1。
本发明制剂的pH为pH3至pH6的范围内,更优选使用pH3-5。
产品形式
根据本发明的头发处理组合物的最终产品形式可以适宜地为,例如洗发香波、调理剂、喷雾剂、摩丝、凝胶剂、蜡状物或洗剂。特别优选的产品形式为洗发香波、洗后调理剂(保留型(leave-in)和漂洗型(rinse-off))和头发处理产品例如洗发精(hair essences)。
对于定型免洗型组合物而言,特别优选例如摩丝、蜡状物和喷雾剂。
洗发香波组合物优选包含一种或多种清洁表面活性剂,其为可化妆用的,并且适于局部应用于头发。也可存在作为乳化剂的另外的表面活性剂。
适宜的清洁表面活性剂选自阴离子表面活性剂、两性表面活性剂和两性离子表面活性剂及其混合物。清洁表面活性剂可以是与乳化剂相同的表面活性剂,或者可以是不同的。
阴离子清洁表面活性剂
根据本发明的洗发香波组合物典型地包含一种或多种阴离子清洁表面活性剂,其为可化妆用的且适于局部应用于头发。
适宜的阴离子清洁表面活性剂的实例为烷基硫酸酯、烷基醚硫酸酯、烷芳基磺酸酯、烷酰基羟乙基磺酸酯、烷基琥珀酸酯、烷基磺基琥珀酸酯、N-烷基肌氨酸酯、烷基磷酸酯、烷基醚磷酸酯、烷基醚羧酸酯和α-烯烃磺酸酯,特别是它们的钠、镁、铵和单、二和三乙醇胺盐。所述烷基和酰基通常包含8至18个碳原子,目可以是不饱和的。所述烷基醚硫酸酯、烷基醚磷酸酯和烷基醚羧酸酯每分子可包含1至10个氧化乙烯或氧化丙烯单元。
典型地在本发明的洗发香波组合物种使用的阴离子清洁表面活性剂包括油基磺基琥珀酸钠、月桂基磺基琥珀酸铵、月桂基硫酸铵、椰油酰基羟乙磺酸钠(sodium cocoyl isethionate)、月桂基羟乙基磺酸钠和N-月桂基肌氨酸钠。最优选的阴离子表面活性剂为月桂基硫酸钠、月桂基醚硫酸(n)EO钠(其中n为1至3)、月桂基硫酸铵和月桂基醚硫酸(n)EO铵(其中n为1至3)。
在本发明的洗发香波组合物中的阴离子清洁表面活性剂的总量通常为总组合物的5至30wt%,优选6至20wt%,更优选8至16wt%。
辅助表面活性剂
洗发香波组合物可任选地包括辅助表面活性剂,优选两性或两性离子表面活性剂,其可以包括的量可为0至约8,优选1至4wt%。
两性和两性离子表面活性剂的实例包括烷基甜菜碱、烷基酰氨基丙基甜菜碱、烷基磺基甜菜碱(sultaines)、烷基氨基乙酸酯、烷基羧基氨基乙酸酯、N-烷酰胺基乙基-N-羟基乙基氨基丙酸钠(alkyl amphopropionates)、N-烷酰胺基乙基-N-羟基乙基氨基乙酸钠(alkylamphoglycinates)、烷基酰氨基丙基羟基磺基甜菜碱(alkyl amidopropyl hydroxysultaines)、酰基牛磺酸酯(acyl taurates)和酰基谷氨酸酯,其中烷基和酰基含有8至19个碳原子。在本发明的洗发香波中使用的典型的两性和两性离子表面活性剂包括月桂基氧化胺、椰油二甲基磺基丙基甜菜碱(cocodimethyl sulphopropyl betaine)和优选的月桂基甜菜碱、椰油酰氨基丙基甜菜碱和N-椰油酰胺基乙基-N-羟基乙基氨基丙酸钠(sodiumcocamphopropionate)。
另一种优选的辅助表面活性剂为非离子表面活性剂,其可以包括的量为总组合物的0至8wt%,优选2至5wt%。
例如,可包括在本发明的洗发香波组合物中的有代表性的非离子表面活性剂包括脂族(C8-C18)、直链或支链伯或仲醇类或酚类与氧化烯的缩合产物,所述氧化烯通常为氧化乙烯且通常含有6至30个氧化乙烯基。
可包括在本发明的洗发香波组合物中的另外的非离子表面活性剂为烷基多糖苷类(alkyl polyglycosides)(APGs)。典型地,APG为包含连接到(任选地通过桥连基)一个或多个糖葡基(glycosyl)的嵌段上的烷基的APG。优选地,APG为下式定义的:
RO-(G)n
其中R为支链或直链C5至C20烷基或者链烯基,G为糖基,n为从1至10。
其它的可包括在本发明的洗发香波组合物中的糖-衍生的非离子表面活性剂包括C10-C18 N-烷基(C1-C6)多羟基脂肪酸酰胺,例如C12-C18 N-甲基葡萄糖酰胺,例如在WO 9206154和US 5194639中描述的,和N-烷氧基多羟基脂肪酸酰胺,例如C10-C18N-(3-甲氧基丙基)葡萄糖酰胺。
所述洗发香波组合物也可以任选地包括一种或多种阳离子辅助表面活性剂,其包含的量可为总组合物的0.01至10,更优选0.05至5,最优选0.05至2wt%。有用的阳离子表面活性剂在本文相关的调理剂组合物中描述。
在本发明的洗发香波组合物中的表面活性剂(包括任意辅助表面活性剂,和/或任意的乳化剂)的总量通常为5至50,优选为5至30,更优选为10至25wt%。
阳离子聚合物
可以存在阳离子聚合物。阳离子聚合物可以是均聚物或由两种或多种类型的单体形成。聚合物的分子量通常为5000至10000000,典型地至少10000,优选为100000至约2000000。聚合物包含阳离子含氮基例如季铵或质子化氨基或其混合物。
适宜的阳离子含氮聚合物描述于CTFA Cosmetic Ingredient Directory,第3版。
阳离子调理聚合物可包含由胺和/或季铵取代的单体和/或可相容的间隔基单体衍生得到的单体单元的混合物。
适宜的阳离子调理聚合物包括1-乙烯基-2-吡咯烷和1-乙烯基-3-甲基-咪唑盐的共聚物(CTFA名:Polyquaternium-16);1-乙烯基-2-吡咯烷和二甲基氨乙基的甲基丙烯酸酯的共聚物(CTFA名:Polyquaternium-11);含有阳离子二烯丙基季铵的聚合物,尤其是(CTFA Polyquaternium 6和Polyquaternium 7,如在美国专利U.S.4,009,256中描述的不饱和羧酸的均聚物和共聚物的氨基-烷基酯的无机酸盐;阳离子聚丙烯酰胺(如在WO95/22311中描述的)。
适宜用于本发明组合物中的阳离子多糖聚合物包括具有葡糖酐残基的那些,例如淀粉或纤维素。阳离子纤维素可以从其Polymer JR(商品名)和LR(商品名)系列的聚合物购自Amerchol Corp.(Edison,NJ,USA),作为羟乙基纤维素与三甲基铵取代的环氧化物反应的盐,工业上(CTFA)也称为Polyquaternium10。另一种类型的阳离子纤维素包括羟乙基纤维素与月桂基二甲基铵取代的环氧化物反应的聚合季铵盐,工业上(CTFA)也称为Polyquaternium 24。这些物质获自Amerchol Corp.(Edison,NJ,USA),商品名为Polymer LM-200。
其它适宜的阳离子多糖聚合物包括含季氮的纤维素醚(例如在美国专利3,962,418中描述的),和醚化的纤维素和淀粉的共聚物(例如在美国专利3,958,581中描述的)。
可使用的特别适宜的阳离子多糖聚合物的类型为阳离子瓜尔胶衍生物,例如guar hydroxypropyltrimonium chloride(以它们的JAGUAR商品名系列售自Rhone-Poulenc)。特别优选的阳离子聚合物为JAGUAR C13S、JAGUAR C14、JAGUAR C15、JAGUAR C17和JAGUAR C16 Jaguar CHT和JAGUAR C162。
在本发明的组合物中,阳离子调理聚合物通常存在的量为总组合物的0.01至5,优选0.05至1,更优选0.08至0.5wt%。
调理表面活性剂
调理组合物通常包含一种或多种可化妆用和适于局部应用于头发的调理表面活性剂。
适宜的调理表面活性剂选自阳离子表面活性剂,单独使用或以混合物使用。
本发明的组合物中应用的阳离子表面活性剂包含氨基或季铵亲水性部分,当将其溶解在本发明的水性组合物中时其带正电荷。
适宜的阳离子表面活性剂的实例为相应于以下通式的那些:
[N(R1)(R2)(R3)(R4)]+(X)-
其中,R1、R2、R3和R4独立地选自(a)1至22个碳原子的脂族基,或(b)具有最多22个碳原子的芳香基、烷氧基、聚氧化烯基、烷基酰胺基、羟烷基、芳基或烷芳基;X为成盐阴离子,例如那些选自卤素(例如氯化物、溴化物)、醋酸根、柠檬酸根、乳酸根、羟乙酸根、磷酸根、硝酸根、硫酸根和烷基硫酸酯基的阴离子。
所述脂族基除了包含碳和氢原子之外,还可以包含醚键和其它基团例如氨基。较长链的脂族基例如约12个或更多碳原子的那些脂族基可以是饱和的或不饱和的。
用于本发明调理组合物的最优选的阳离子表面活性剂为单烷基季铵化合物,其中烷基链长为C16至C22。
适宜的阳离子表面活性剂的实例包括季铵化合物,尤其是三甲基季铵化合物。
优选的季铵化合物包括氯化十六烷基三甲基铵、氯化苄基三甲基铵(BTAC)、西吡氯铵、氯化四甲铵、氯化四乙铵、氯化辛烷基三甲基铵、氯化十二烷基三甲基铵、氯化十六烷基三甲基铵、氯化辛基二甲基苄基铵、氯化癸基二甲基苄基铵、氯化硬脂基二甲基苄基铵、氯化双十二烷基二甲基铵、氯化双十八烷基二甲基铵、氯化牛脂三甲基铵、氯化椰油三甲基铵(cocotrimethylammonium chloride)、氯化PEG-2油基铵及这些化合物的盐,其中氯化物可以被卤素(例如溴化物)、乙酸盐、柠檬酸盐、乳酸盐、乙醇酸盐、磷酸盐、硝酸盐、硫酸盐或烷基硫酸盐代替。更适宜的阳离子表面活性剂包括具有CTFA命名的那些材料:Quaternium-5,Quaternium-31和Quaternium-18。任何前述材料的混合物也都是适宜的。在本发明的头发调理剂中使用的特别有用的阳离子表面活性剂为氯化十六烷基三甲基铵,例如以GENAMIN CTAC,ex HoechstCelanese市售。
脂肪伯胺、脂肪仲胺和脂肪叔胺的盐也是适宜的阳离子表面活性剂。这些胺的烷基优选地具有12至22个碳原子,可以是取代的或非取代的。
特别有用的为酰氨基取代的脂肪叔胺,特别是具有一个C12至C22烷基或链烯基链的叔胺。本文使用的这类胺包括硬脂酰氨基丙基二甲基胺、硬脂酰氨基丙基二乙基胺、硬脂酰氨基乙基二乙基胺,硬脂酰氨基乙基二甲基胺、棕榈酸酰氨基丙基二甲基胺、棕榈酸酰氨基丙基二乙基胺、棕榈酸酰氨基乙基二乙基胺、棕榈酸酰氨基乙基二甲基胺、二十二烷酸酰氨基丙基二甲基胺、二十二烷酸酰氨基丙基二乙基胺、二十二烷酸酰氨基乙基二乙基胺、二十二烷酸酰氨基乙基二甲基胺、花生酸酰氨基丙基二甲基胺(rachidamidopropyldimethylamine)、花生酸酰氨基丙基二乙基胺、花生酸酰氨基乙基二乙基胺、花生酸酰氨基乙基二甲基胺、二乙基氨基乙基硬脂酰胺。也有用的是二甲基十八胺、二甲基豆胺、豆胺(soyamine)、肉豆蔻基胺、十三烷基胺、乙基硬脂酰胺、N-牛脂丙二胺、乙氧基化的(具有5摩尔的氧化乙烯)硬脂胺、二羟乙基硬脂胺和花生烷基(arachidyl)二十二烷基胺。
这些胺典型地用于与酸结合以提供阳离子种类。本文应用的这些优选的酸包括L-谷氨酸、乳酸、盐酸、苹果酸、琥珀酸、醋酸、富马酸、酒石酸、柠檬酸、L-谷氨酸盐酸盐及其混合物;更优选L-谷氨酸、乳酸、柠檬酸。在本发明中所用的那些中包括的阳离子胺表面活性剂公开于Nachtiga等的美国专利4,275,055(1981年6月23日授权)中的那些。
质子化胺与来自酸的H+的摩尔比率优选为约1∶0.3至1∶1.2,更优选为约1∶0.5至约1∶1.1。
在本发明的调理剂中,阳离子表面活性剂的含量优选为总组合物的0.01至10,更优选为0.05至5,最优选为0.1至2wt%。
在这一部分中详细描述的阳离子表面活性剂也适用于本发明的其它方面,其中在将调理物质加入到最终的头发调理组合物之前,将阳离子表面活性剂与thermotropic mesogenic material和与油性调理物质紧密混合。
脂肪物质
本发明的调理组合物优选还包含脂肪物质。在调理组合物中脂肪物质与阳离子表面活性剂的组合应用被认为是特别有利的,因为这将导致形成阳离子表面活性剂分散在其中的结构相。
“脂肪物质”指脂肪醇、烷氧基化脂肪醇、脂肪酸或其混合物。
优选地,脂肪物质的烷基链为完全饱和的。
有代表性的脂肪物质包含8至22个碳原子,更优选16至22个碳原子。适宜的脂肪醇的实例包括鲸蜡醇、硬脂醇及其混合物。使用这些物质也是有利的,因为它们有助于本发明组合物的整体调理性质。
在烷基链上具有约12至约18个碳原子的烷氧化(例如乙氧化的或丙氧化)脂肪醇可代替脂肪醇本身使用,或除脂肪醇本身此之外可使用这类物质。适宜的实例包括乙二醇鲸蜡醚、聚氧乙烯(2)硬脂醚、聚氧乙烯(4)鲸蜡醚及其混合物。
在本发明的调理剂中的脂肪醇物质的含量适宜地为0.01至15,优选为0.1至10,更优选0.1至5wt%。阳离子表面活性剂与脂肪醇的重量比适宜地为10∶1至1∶10,优选为4∶1至1∶8,最适宜为1∶1至1∶7,例如1∶3。
混悬剂
在优选的实施方案中,头发处理组合物,尤其是如果它是洗发香波组合物,进一步包含0.1至5wt%的混悬剂。适宜的混悬剂选自聚丙烯酸、丙烯酸的交联聚合物、丙烯酸与疏水性单体的共聚物、包含羧酸的单体与丙烯酸酯的共聚物、丙烯酸和丙烯酸酯的交联共聚物、杂多糖胶(heteropolysaccharide gums)和结晶的长链酰基衍生物。期望的长链酰基衍生物选自乙二醇硬脂酸酯、具有16至22个碳原子的脂肪酸的烷醇酰胺及其混合物。乙二醇二硬脂酸酯和聚乙二醇3二硬脂酸酯是优选的长链酰基衍生物。聚丙烯酸以Carbopol 420、Carbopol488或Carbopol 493市售。也可使用丙烯酸与多功能药剂交联的聚合物,它们以Carbopol 910、Carbopol 934、Carbopol 941和Carbopol 980市售。含有羧酸的单体和丙烯酸酯的适宜共聚物的实例为Carbopol 1342。所有的Carbopol(商品名)物质购自Goodrich。
适宜的丙烯酸和丙烯酸酯的交联共聚物为Pemulen TR1或Pemulen TR2。适宜的杂多糖胶为黄原胶,例如以Kelzan mu出售。
调理剂
硅氧烷调理剂
本发明的组合物可包含硅氧烷调理剂的乳化的小滴,用于增强调理特征。
适宜的硅氧烷包括聚二有机硅氧烷,尤其是具有CTFA命名的二甲硅油(dimethicone)的聚二甲基硅氧烷。也适宜用于本发明的组合物(尤其是洗发香波和调理剂)的为具有羟基端基的聚二甲基硅氧烷,其CTFA命名为聚二甲基硅烷醇(dimethiconol)。也适宜用于本发明的组合物的为具有少量交联度的硅氧烷胶,例如在WO 96/31188中描述的。
在25℃下,乳化的硅氧烷本身(不是乳剂或最终的头发调理组合物)的粘度典型地为至少10,000 cst,硅氧烷自身的粘度优选为至少60,000 cst,最优选为至少500,000 cst,理想地至少为1,000,000 cst。为便于配制优选的粘度不超过109cst。
在本发明的洗发香波组合物中所用的乳化的硅氧烷典型地具有在组合物中的平均硅氧烷小滴粒径小于30,优选小于20,更优选小于10μm,理想地为0.01至1μm。具有≤0.15μm的平均硅氧烷小滴粒径的硅氧烷乳剂通常称为微乳剂。
适宜的预形成的乳剂的实例包括乳剂DC2-1766、DC2-1784、DC-1785、DC-1786和微乳剂DC2-1865和DC2-1870,所有都购自Dow Corning。这些都是聚二甲基硅烷醇(dimethiconol)的乳化剂/微乳剂。交联的硅氧烷胶也以预乳化的形式市售,其对于方便配制有利。优选的实例为购自Dow Corning的如DC X2-1787的物质,其为交联的聚二甲基硅烷醇(dimethiconol)胶的乳剂。进一步优选的实例为购自Dow Corning的DC X2-1391物质,其为交联聚二甲基硅烷醇(dimethiconol)胶的微乳剂。
包括在本发明的洗发香波和调理剂中的进一步优选类型的硅氧烷为氨基功能基硅氧烷。“氨基官能基硅氧烷”指含有至少一个伯胺、仲胺或叔胺基或季铵基的硅氧烷。适宜的氨基官能基硅氧烷的实例包括具有CTFA命名的“氨基二甲基硅氧烷(aminodimethicone)”的聚硅氧烷。
在本发明中应用的适宜的氨基官能基硅氧烷的特定的实例为氨基硅氧烷油类DC2-8220、DC2-8166、DC2-8466和DC2-8950-114(所有都购自Dow Corning)和GE 1149-75(购自General Electric Silicones)。适宜的季硅氧烷聚合物描述于EP-A-0530974。优选的季硅氧烷聚合物为K3474,购自Goldschmidt。
也适宜的为含非离子和/或阳离子表面活性剂的氨基官能硅氧烷油类的乳剂。预形成的氨基官能基硅氧烷乳化剂也购自硅氧烷油类的供应商,如DowCorning和General Electric。特别的实例包括DC929阳离子乳剂、DC939阳离子乳剂和非离子乳剂DC2-7224、DC2-8467、DC2-8177和DC2-81 54(所有购自Dow Corning)。
对于某些洗发香波而言,特别优选使用氨基和非氨基官能基硅氧烷的组合。硅氧烷的总量优选为总组合物的0.01至10wt%,更优选为0.3至5;最优选0.5至3wt%为适宜的水平。
(ii)非硅氧烷油性调理剂组分
根据本发明,组合物也可包含分散的、非挥发性的、水不溶的油性调理剂。
“不溶的”指物质在水(蒸馏的或等同物)中不溶,在25℃下浓度为0.1%(w/w)。
适宜的油性或脂肪物质选自烃油类、脂肪酯类及其混合物。直链的烃油类优选含有约12至约30个碳原子。链烯基单体,例如C2-C6链烯基单体的聚合烃类也是适宜的。
适宜的烃油类的具体实例包括石蜡油、矿物油、饱和的和不饱和的十二烷、饱和的和不饱和的十三烷、饱和的和不饱和的十四烷、饱和的和不饱和的十五烷、饱和的和不饱和的十六烷及其混合物。也可以使用这些化合物的支链异构体,以及更长链的烃类。
适宜的脂肪酯的特征在于具有至少十个碳原子,并且包括由脂肪酸或醇衍生的烃链酯类,单羧酸酯类包括式R’COOR的醇和/或酸的酯,其中R’和R独立地代表烷基或链烯基,在R’和R中的碳原子总和为至少10,优选为至少20。也可使用羧酸的二和三烷基和链烯基酯。
特别优选的脂肪酯为甘油单酯、甘油二酯和甘油三酯,更特别地为甘油和长链羧酸例如C1-C22羧酸的单、二和三酯。优选的物质包括可可脂、棕榈硬脂精(palm stearin)、葵花油、大豆油和椰子油。
油类或脂肪物质适宜存在的量为0.05至10,优选为0.2至5,更优选为约0.5至3wt%。
在包含调理剂的头发处理组合物中,优选地还存在阳离子聚合物。
定型聚合物
如果产物是定型产品,优选存在定型聚合物。
如果存在头发定型聚合物,优选地在本发明的组合物中的存在量为0.001%至10%重量,更优选为0.1%至10%重量,例如从1%至8%。
头发定型聚合物是公知的。适宜的头发定型聚合物包括市售聚合物,其包含提供聚合物性质上为阳离子、阴离子、两性或非离子的部分。适宜的头发定型聚合物包括,例如嵌段和接枝共聚物。聚合物可以是合成的或天然产生的。
助剂
本发明的组合物也可包含适于头发护理的助剂。通常,这样的成分独立被包含的含量最高为总组合物的2wt%,优选最高为1wt%。
适宜的头发护理助剂包括氨基酸和神经酰胺。
本发明现在可进一步通过下述非限制性的实施例来阐述。
数字编号的是本发明的实施例;字母编号的是比较例。
除非另有说明,引证的所有百分比为基于总重量的重量百分比。
具体实施方式
实施例
在用包含活性成分的洗发香波基质处理前和处理后,进行测定单个头发纤维的抗扭刚度(torsional stiffness)的试验,以测定活性分子对头发物理性质的影响。在12∶2(SLES∶CAPB)基质洗发香波中洗涤(2×30s)和冲洗(2×30s)单个头发纤维,然后在22℃和50%相对湿度下储存12小时以保持平衡。
下表显示了用于处理纤维的基质制剂的细节。
12∶2基质 | 12∶2基质+活性成分 | |
月桂基醚硫酸钠(2EO) | 12 | 12 |
椰油酰氨基丙基甜菜碱 | 2 | 2 |
海藻糖 | 0.40 | |
己二酸 | 0.10 | |
活性成分 | 0.10 | |
水 | 至100 | 至100 |
注:SLES=月桂基醚硫酸钠~2EO
CAPB=椰油酰氨基丙基甜菜碱
平衡后,将纤维的一端连接到传动器(motor),另一端连接到扭摆上。启动传动器使纤维旋转135o后停止。在传动器停止后,然后测定扭摆的振动周期。
然后采用与如上相同的步骤清洗上述使用的相同的纤维,但是使用12∶2(SLES∶CAPB)基质洗发香波,其还包含海藻糖(0.4wt%)、己二酸(0.1wt%)和其它的活性成分(0.1wt%)-用少量柠檬酸或NaCl(没有记录质量)调节包含活性成分的制剂的pH为pH5.5。然后在与上述相同的条件下使纤维平衡12小时。然后对这些处理的纤维,如上所述测定扭转振动周期。
所测试的与海藻糖和己二酸组合的活性化合物为:
实施例A 碳酸胍(Guanadine carbonate)
实施例B 碳酸钠
实施例C 磷酸钠
实施例D 硫酸钠
实施例1 碳酸铵
实施例2 磷酸氢铵
下表含处理之前(仅用基质洗涤)和用各种在12∶2基质中的活性成分组合处理后纤维的扭转振动周期数据。
该表显示出碳酸铵和磷酸氢铵增加了接受这些处理的头发纤维的扭转振动周期,然而硫酸钠降低了扭转振动周期。振动周期的增加表示抗扭刚度的降低,而振动周期的降低表示抗扭刚度的增加。
海藻糖(0.4wt%)+己二酸(0.1wt%)+碳酸胍(0.1wt%) | 海藻糖(0.4wt%)+己二酸(0.1wt%)+碳酸钠(0.1wt%) | 海藻糖(0.4wt%)+己二酸(0.1wt%)+磷酸钠(0.1wt%) | 海藻糖(0.4wt%)+己二酸(0.1wt%)+硫酸钠(0.1wt%) | 海藻糖(0 4wt%)+己二酸(0.1wt%)+碳酸铵(0.1wt%) | 海藻糖(0.4wt%)+己二酸(0.1wt%)+磷酸氢铵(0.1wt%) | 海藻糖(0.4wt%)+己二酸(0.1wt%)+碳酸铵(0.1wt%) | |||||||
处理前 | 处理后 | 处理前 | 处理后 | 处理前 | 处理后 | 处理前 | 处理后 | 处理前 | 处理后 | 处理前 | 处理后 | 处理前 | 处理后 |
5.7134.5645.6405.1346.2444.7595.1523.7005.2777.8765.1757.8156.2335.7174.0534.3194.6045.859 | 5.7274.5705.5915.1326.2374.7625.1993.7325.2707.8005.1947.6596.2895.7074.0844.3594.5845.885 | 4.4484.7025.0375.4274.5075.3024.1464.4394.1005.0344.5393.8793.6824.3414.3975.5866.5974.2815.6924.474 | 4.4094.7165.0545.4254.4865.3434.1564.4514.0805.0324.5343.8803.6894.3024.3615.5356.5444.2735.6854.442 | 6.4045.0353.4417.6175.3594.6095.5444.7895.0655.7994.8197.7408.5035.2755.0885.0334.3266.9905.0025.999 | 6.4154.9773.4317.6385.4254.5825.5364.7965.0705.7964.8427.8248.5135.3785.0965.0364.3287.0465.0335.077 | 5.0874.9526.6824.5657.1294.8934.8153.8925.1004.6274.6825.6565.4975.3324.1686.6154.6153.7165.1575.400 | 5.0014.9056.6414.5047.0354.8024.7433.8575.0124.5804.6175.5995.4255.2714.1238.4814.5443.6275.0885.327 | 4.3984.1363.9074.5755.4414.3214.7264.2584.6585.8924.7584.2264.9288.1453.8753.7113.7706.8265.5507.034 | 4.4954.2323.9794.6605.5934.4114.8814.3774.7335.9984.8564.3125.0606.1593.9233.7623.8356.9465.6657.113 | 4.7615.6534.9764.2774.6235.0584.1894.8457.4916.4045.7445.6354.7164.3804.1766.1795.855 | 4.9855.8915.2254.4734.8515.3134.4285.0667.8835.7496.0515.8684.9154.5864.3776.552 | 5.1915.7718.6963.9844.0375.3515.3714.9605.4105.1715.9315.7514.4374.2985.9703.7064.8198.5355.0083.579 | 5.3055.9808.9524.1134.1815.4935.4685.0995.6425.3586.1175.9554.5414.3325.9683.7314.8098.5015.0743.611 |
在含铵的组合中观察到的刚度的降低将被消费者感知,因为当采用含铵的组合物处理后提供更柔顺和更柔软的头发。这也可从消费者的家用(in-homes)试验结果中反映出:其中发现当与硫酸钠的组合相比时,发现有更多的增加水分的感觉(显著)、更柔顺的感觉(显著)。
制备下述的实施例:
制备下述基质洗发香波组合物:
实施例3 | |
月桂基醚硫酸钠(2EO) | 12 |
椰油酰氨基丙基甜菜碱 | 2 |
海藻糖 | 0.40 |
己二酸 | 0.10 |
碳酸铵 | 0.10 |
水 | 至100 |
表3-洗发香波制剂
Wt% | |
成分 | 实施例4 |
月桂基醚硫酸钠(2EO) | 12 |
椰油酰氨基丙基二甲基氨基乙酸 | 2 |
硅氧烷乳剂 | 2 |
瓜尔胶羟丙基三甲基氯化铵(Guar hydroxypropyltrimethylammonium chloride) | 0.30 |
防腐剂 | 0.35 |
香料 | 0.42 |
柠檬酸 | 0.17 |
海藻糖 | 0.40 |
己二酸 | 0.10 |
碳酸铵 | 0.10 |
水和微量成分(minors) | 加至100wt% |
表4摩丝制剂
成分 | 基质制剂 | 原材料供应商 |
CF2259(50%活性成分)交联聚二甲基硅氧烷醇乳剂 | 3 | Toray DowCorning |
HC聚合物3M(20%活性成分)Polyquaternium 11 | 3.0 | Osaka OrganicChemicals |
Volpo CS50乙氧基(50)十六/十八烷醇 | 0.3 | CrodaOleochemicals |
乙醇 | 8 | |
水 | 加至100% | |
CAP40 | 8 | Calor |
下述实施例是通过将下列成分加入到基质制剂中制备的:
成分 | 实施例1 | 实施例2 | 实施例3 | 实施例C |
海藻糖,得自SigmaChemicals | 0.4 | 0.2 | 0.6 | - |
己二酸,得自SigmaChemicals | 0.1 | 0.05 | 0.15 | - |
碳酸铵,得自SigmaChemicals | 0.1 | 0.05 | 0.15 | - |
已发现,与比较例相比,可看到本发明所有的制剂有最好的卷曲效果(definiton)和最小的体积。在周围环境和潮湿的条件下,用本发明的实施例处理的头发保持其形状(shape)和形态(form)良好。
Claims (17)
1.头发处理组合物,其包含占总组合物的0.05至8wt%的i)二糖;ii)二酸,和iii)铵离子源。
2.根据权利要求1的头发处理组合物,其中铵离子源为碳酸铵。
3.根据权利要求1或2的头发处理组合物,其中二糖具有两个己糖环。
4.根据任一前述权利要求的头发处理组合物,其中二糖选自海藻糖、纤维素二糖或其混合物。
5.根据任一前述权利要求的头发处理组合物,其中二糖为海藻糖。
6.根据任一前述权利要求的头发处理组合物,其中二酸具有下式:
HOOC-(CH2)n-COOH
其中n为从2至8的整数。
7.根据权利要求6的头发处理组合物,其中n等于2或4。
8.根据权利要求7的头发处理组合物,其中二酸为己二酸。
9.根据任一前述权利要求的头发处理组合物,其中碳酸铵的含量为总组合物的0.01wt%至2.0wt%。
10.根据任一前述权利要求的头发处理组合物,其还进一步包含表面活性剂。
11.根据任一前述权利要求的头发处理组合物,其包含含水基质。
12.根据任一前述权利要求的组合物用于头发定型的用途。
13.根据任一前述权利要求的组合物用于使头发光滑的用途。
14.根据权利要求1至11中任一项的组合物用于使头发整齐的用途。
15.根据权利要求1至11中任一项的组合物用于防止头发损伤的用途。
16.一种处理头发的方法,其包含给头发施用权利要求1至11中任一项的组合物。
17.一种制备根据权利要求1至11中任一项的头发处理组合物的方法,包含将二酸加入到碳酸盐离子源中的步骤。
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US4390625A (en) * | 1981-02-06 | 1983-06-28 | Richter Gedeon Vegyeszeti Gyar Rt | Method for controlling the amount and distribution of alkaloids formed in a fermentation process |
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