CN113164365A - 用于抑制脱发或皮肤炎症的组合物 - Google Patents
用于抑制脱发或皮肤炎症的组合物 Download PDFInfo
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- CN113164365A CN113164365A CN201980078316.3A CN201980078316A CN113164365A CN 113164365 A CN113164365 A CN 113164365A CN 201980078316 A CN201980078316 A CN 201980078316A CN 113164365 A CN113164365 A CN 113164365A
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- Prior art keywords
- composition
- skin inflammation
- inhibiting
- hair loss
- alopecia
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Abstract
本发明涉及一种用于抑制脱发或皮肤炎症的组合物,包含:穗花杉双黄酮(Amentoflavone);以及选自由柏子仁提取物、染料木素(Genistein)以及鹰嘴豆芽素A(Biochanin A)组成的组中的一种以上的成分。
Description
技术领域
本申请主张基于2018年11月29日提出的韩国专利申请第10-2018-0150304号的优先权的利益,并且该韩国专利申请文献中公开的全部内容作为本说明书的一部分包含在本说明书中。
本发明涉及一种具有前列腺素D2合成酶(prostaglandin D2 synthase,PTGDS)活性抑制效果的用于脱发或皮肤炎症的组合物,更详细地涉及一种通过优异的前列腺素D2合成酶活性抑制效果来抑制脱发或皮肤炎症的组合物,包含穗花杉双黄酮(Amentoflavone);以及选自由柏子仁提取物、染料木素(Genistein)以及鹰嘴豆芽素A(Biochanin A)组成的组中的一种以上的成分。
背景技术
通常,脱发的原因可以举出遗传因素、药物服用、老化的进行、放射治疗以及重病后压力等。另外,众所周知,从生化或生理学角度来看,脱发现象是由于过度活动、头皮血液循环的问题以及毛发代谢所必需的营养素的缺乏引起的。这些因素通过单独或复合而加速脱发且加重症状。尤其,由于遗传因素或后天因素导致男性荷尔蒙的生成、变化、识别以及信号传递过程过度地进展,因此当毛囊组织早期老化时,脱发症加重的概率会增加。
为了治疗脱发,到目前为止进行了各种尝试,作为外科的方法具有基于头皮皮瓣术、脱发部位缩小术以及组织扩张术的头皮整形术与自身毛发移植术等。所述外科治疗方法在效果方面有优势,但缺点是因患者的经济、精神负担非常大而难以广泛使用。
除此之外,各种治疗剂正在使用中,代表性的外用制剂即米诺地尔(Minoxidil)具有毛细血管扩张功能,涂抹在头皮上,从而防止脱发,但是具有在瘙痒、刺激等的副作用和脱发治疗中,还没有明确表明主动靶向的问题。众所周知,内服药即非那雄胺(Finasteride)具有抑制诱发脱发的男性荷尔蒙5α-双氢睾酮(5α-dihydrotestosterone,DHT)生成的作用,服用6个月到1年左右时表现生发或抑制脱发的效果,但是存在如果停止服用,则在2个月内恢复原状的问题,据悉可能发生生殖能力障碍等的副作用。
因此,实际上持续要求一种无副作用且对人体无害的同时具有抑制脱发效果的脱发抑制剂的开发。
前列腺素D2合成酶(Prostagladin D2 Synthase,PTGDS)作为生成前列腺素D2(prostaglandin D2,PGD2)的酶,已发现前列腺素D2在与在没有脱发症的男性头皮上相比,以更高的水平存在于具有脱发症的男性头皮上,因此被认为引起脱发的重要因素(Garzaet al.(2012)Sci.Transl.Med.4126ra34)。另外,已发现前列腺素D2合成酶通过前列腺素D2来调节炎症反应(R.Rajakariar et al.PNAS,2007,104,20979-20984),并作为炎症反应的介质,能够抑制前列腺素D2合成酶的活性而阻碍炎症反应。
因此,本发明人确认通过抑制前列腺素D2合成酶的活性来抑制皮肤炎症反应的同时,还可以抑制脱发反应,从而完成了本发明。
[现有技术文献]
[专利文献]
(专利文献1)韩国授权专利第10-1766752号(含有米诺地尔的药剂学组合物)
(专利文献2)韩国公开专利第10-2015-0046332号(聚合非那雄胺纳米粒子、包含其的水性组合物、用于治疗脱发的组合物及其制备工程以及其组合物的用途)
发明内容
本发明人为了解决如上所述的问题,以提供持续使用带来的副作用小且有效抑制脱发以及皮肤炎症的组合物为目的。
为了达到所述目的,根据本发明的一实施例的用于抑制脱发或皮肤炎症的组合物包含穗花杉双黄酮(Amentoflavone)以及选自由柏子仁提取物、染料木素(Genistein)以及鹰嘴豆芽素A(Biochanin A)组成的组中的一种以上的成分。
可以是,所述穗花杉双黄酮(Amentoflavone)相对于所述组合物总重量含有0.1ppm至1,000ppm。可以是,穗花杉双黄酮是从选自由佛手、卷柏、拳柏、扁柏以及银杏组成的组中的一种以上提取而成的。
可以是,所述柏子仁提取物相对于所述组合物总重量含有10ppm至10,000ppm。
可以是,染料木素(Genistein)相对于所述组合物总重量含有1ppm至1,000ppm。可以是,染料木素从选自由豆、异黄酮(Isoflavone)组成的组中的一种以上提取而成的。
可以是,所述鹰嘴豆芽素A(Biochanin A)相对于所述组合物总重量含有10ppm至1,000ppm。可以是,鹰嘴豆芽素A从选自由降香、豆、红三叶以及异黄酮(Isoflavone)组成的组中的一种以上提取而成的。
可以是,所述组合物抑制体内前列腺素D2合成酶(Prostagladin D2Synthase,PTGDS)的活性。可以是,所述用于抑制脱发或者皮肤炎症的组合物包含化妆料,化妆料的剂型选自溶液、面霜、乳液、洗发水、护发素、喷雾剂以及凝胶中。
可以是,所述用于抑制脱发或者皮肤炎症的组合物通过经皮注射或皮下注射投入到人体中,并且选自皮肤外用制剂或口服给药制剂中。
可以是,所述皮肤包括毛囊以及头皮。
本发明所提供的组合物在穗花杉双黄酮(Amentoflavone)中含有选自由柏子仁提取物、染料木素(Genistein)以及鹰嘴豆芽素A(Biochanin A)组成的组中的一种以上的成分,从而能够取得抑制脱发或皮肤炎症的协同效果。另外,本发明的用于抑制脱发或者皮肤炎症的组合物使用了天然物质而能够长时间使用的同时没有副作用。
附图说明
图1是示出根据本发明的一实施例的通过酶联免疫吸附试验(ELISA)方法来显示前列腺素D2合成酶的前列腺素D2生成抑制效果的结果的图表。
具体实施方式
以下,为了有助于理解本发明,对本发明进行更详细地说明。
对在本发明中作为有效成分使用的穗花杉双黄酮(Amentoflavone)的抗氧化作用(Mora A.et al.,Biochem.Pharmacol.,40(4),pp793-7,1990)、淋巴细胞增殖(lymphocyteproliferation)抑制作用(Lee SJ.et al.,Life Sci.,57(6),pp551-558,1995)、磷脂酶(phospholipase)C-γ1酶活性抑制作用(Lee HS.et al.,Planta.Med.,1996,62(4),pp293-296)、抗艾滋病病毒作用、通过抑制环氧化酶(cyclooxygenase)以及脂氧合酶(lipoxygenase)的抗炎作用(Kim HP.et al.,Prostaglandins Leukot Essent FattyAcids,58(1),pp17-24,1998)、cAMP-磷酸二酯酶(cAMP-phosphodiesterase)抑制作用、病毒的抗生作用、抗菌作用等进行了研究(Kim HK.et al.,Arch.Pharm.Res.,21(4),pp406-410,1998;Lin YM.et al.,Planta.Med.,65(2),pp120-125,1999;Krauze-BaranowskaM.et al.,Planta.Med.,65(6),pp572-573,1999)。
穗花杉双黄酮可以从选自由佛手、卷柏、拳柏、扁柏以及银杏组成的组中的一种以上提取而成。佛手是属于佛手科的多年生草本,生长约5~20cm左右,其特征在于从底部衍生出来的根茎非常坚硬且短,长出很多须根。卷柏是属于佛手科的维管植物,其特征在于在岩石上生长,地下茎伸向地下或苔藓植物之间,末端笔直生长。拳柏属于佛手科,是一种滋生在岩石上的隐花植物,晒干后呈拳头形状而得名。扁柏是柏树科的常绿乔木,叶子是倒卵型或卵形,两面都是绿色或浅黄绿色。银杏是银杏科的落叶乔木,叶子呈扇形,从中央分两叉,但有不分叉和分两叉以上等。
穗花杉双黄酮(Amentoflavone)由以下化学式1表示。
<化学式1>
在本发明中,作为有效成分使用的柏子仁(Thujae semen)是柏树(Thujaorientalis(occidentalis)(柏树科)Curpressaceae)的种子,呈卵圆形到长椭圆形或长圆柱形。据悉,柏子仁在东医宝鉴三圣膏处方中,使脱落的胡须和头发重新生长出来,并包含在四圣不老丹和斑龙丸等的主要出现身体虚弱或老化症状时使用的处方中。另外,经现代科学方面的证实,在两种动物模型中,毛发生长活性显示较高而调节雌激素转化,由此能够作为对脱毛症有用的物质来使用。
在本发明中,例如可以通过以下方法制备柏子仁提取物。将柏子仁用2倍容量的95%乙醇进行提取而过滤、浓缩后加入5倍容量的水和5倍容量的乙酸乙酯进行震荡而分离层。利用硫酸镁去除乙酸乙酯层的水分,通过过滤、浓缩而获得柏子仁提取物。
在本发明中,作为有效成分使用的染料木素(Genistain)其为植物界的雌激素类似物,具有强烈的抗氧化效果、抗炎效果、抗癌效果的同时,促进正常细胞的复制。作为抑制脱发的成分发表过SCI级临床论文,而且最近还报告了作为抑制光老化的物质的临床结果。在一实现例中,染料木素具有作为雌激素类似物的荷尔蒙效果、细胞再生效果、光老化抑制效果、抑制脱发以及促进毛发生长的作用。染料木素为多酚的一种,例如可以从大豆异黄酮(isoflavone)中分离提取,但不限于此。
染料木素(Genistein)由以下化学式2表示。
<化学式2>
在本发明中作为有效成分使用的鹰嘴豆芽素A(Biochanin A),例如可以从选自由降香、豆、红三叶以及异黄酮组成的组中的一种以上分离,但不限于此。
鹰嘴豆芽素A(Biochanin A)由以下化学式3表示。
<化学式3>
在本发明的一实施例中,与将穗花杉双黄酮作为单独有效成分包含的组合物相比,当包含选自由柏子仁提取物、染料木素以及鹰嘴豆芽素A组成的组中的一种以上的成分而进行组合时,确认到抑制前列腺素D2合成酶活性的效果更优异。
即,本发明提供如下组合物,可以通过有效地抑制前列腺素D2合成酶的活性,减少引起脱发的因素即前列腺素D2的生成而抑制脱发反应,并抑制皮肤上产生的炎症反应。
在本发明的一实施例中,所述组合物可以用作药学组合物。
所述药学组合物除了包含穗花杉双黄酮与选自由柏子仁提取物、染料木素以及鹰嘴豆芽素A组成的组中的一种以上的成分的有效成分之外,可以进一步含有防腐剂、稳定剂、水合剂或乳化促进剂、用于调节渗透压的盐和/或缓冲剂等的药剂学辅助剂以及其他治疗上有用的物质,根据常规的方法,可以配制成各种口服给药制剂或非口服给药制剂形态。
所述口服给药制剂为例如,片剂、丸剂、硬胶囊和软胶囊、液体制剂、悬浮剂、乳化剂、糖浆剂、粉剂、栓剂、细粒剂、颗粒剂、微丸剂等,这些剂型除了有效成分之外,可以含有表面活性剂、稀释剂(例:乳糖、葡萄糖、蔗糖、甘露醇、山梨醇、纤维素以及甘氨酸)、润滑剂(例:二氧化硅、滑石粉、硬脂酸及其镁或钙盐以及聚乙二醇)。片剂还可以含有镁铝硅酸盐、淀粉膏、黄芪胶、甲基纤维素、羧甲基纤维素钠以及聚乙烯吡咯啶之类的结合剂,根据情况,可以含有淀粉、琼脂、海藻酸或其钠盐之类的崩解剂、吸收剂、着色剂、芳香剂以及甜味剂等的药剂学添加剂。所述片剂可以通过常规的混合、颗粒化或涂层方法来制备。
另外,作为所述非口服给药形态可以为经皮、皮下、静脉以及肌肉给药型剂型,例如,可以为注射剂、点滴剂、软膏、乳液、凝胶、面霜、喷雾剂、悬浮剂、乳剂、佐剂、贴剂等剂型,但不限于此。
所述有效成分的投入量决定在于通常的技术人员的水平内,药物的1日给药量根据待给药对象的进展程度、发病时期、年龄、健康状态、并发症等各种因素而不同,当以成人为基准时,在一方面,可以将所述组合物按1μg/kg~200mg/kg,在另一方面,按50μg~50mg/kg的量每天分1次至3次进行给药,所述给药量并不是用任何方法来限定本发明的范围。
所述药学组合物可以为皮肤外用制剂,所述皮肤外用制剂作为可以包括任何在皮肤外部上涂抹的总称,各种剂型的医药品可以包括在其中。
在本发明的一实施例中,所述组合物可以用作化妆料组合物。在所述化妆料组合物中,除了乳酸乳球菌W-Camellia菌株的溶出物之外,可以进一步包含功能性添加物以及包含在常规化妆料组合物中的成分。作为所述功能性添加物可以包含选自由水溶性维生素、油溶性维生素、高分子肽、高分子多糖、鞘脂以及海藻提取物组成的组中的成分。作为除此之外所包含的调配成分可以举出油脂成分、保湿剂、润滑剂、表面活性剂、有机和无机颜料、有机粉体、紫外线吸收剂、防腐剂、杀菌剂、抗氧化剂、植物提取物、pH调节剂、醇、色素、香料、血液循环促进剂、冷感剂、止汗剂、净化水等。
所述化妆料组合物的剂型不受特别限定,根据所需目的,可以适当地进行选择。例如,可以制备成选自由润肤液、柔肤水、爽肤水、收敛水、乳液、牛奶润肤露、保湿乳液、营养乳液、按摩霜、营养霜、保湿霜、护手霜、粉底、精华液、营养精华液、面膜、香皂、泡沫洗面奶、卸妆乳、洁面霜、身体乳以及沐浴乳组成的组中的一种以上的剂型,但不限于此。
另外,所述化妆料组合物可以通过含有化妆品学或皮肤科学可接受的介质或机制而剂型化。其作为适合局部用的所有剂型,例如,可以提供为如下形态:将在溶液、凝胶、固体、面团无水产物、水相中分散油相而获得的乳液、悬浮液、微乳液、微胶囊、微粒球或离子型(脂质体)以及非离子型的小囊分散剂的形态,或者面霜、爽肤水、乳液、粉饼、软膏、喷雾剂或遮瑕棒的形态。另外,还可以用作泡沫(foam)形态或进一步含有压缩推进剂的气溶胶组合物的形态。这些组合物可以根据本技术领域中的常规方法制得。
不仅如此,所述化妆料组合物可以用作头皮用或毛发用组合物等。因此,所述化妆料组合物可以配制成在头皮和毛发上一起使用的剂型,例如洗发水、护发素、护发素、头皮调理乳、发膜、头皮毛发两用发膜、防脱发毛发用发膜、受损头发用发膜、免洗(leave-in)护发素、冲洗(wash-off)护发素或护发精华液等头皮或毛发、头皮和毛发两用产品等。
在本发明的剂型为糊剂、面霜或凝胶的情况下,可以利用动物纤维、植物纤维、蜡、石蜡、淀粉、黄芪胶、纤维素衍生物、聚乙二醇、硅、膨润土、二氧化硅、滑石粉或氧化锌等作为载体成分。
在本发明的剂型为散粉或喷雾剂的情况下,可以利用乳糖、滑石粉、二氧化硅、氢氧化铝、硅酸钙或聚酰胺粉末作为载体成分,尤其是喷雾剂的情况下,可以进一步包含氯氟烃、丙烷/丁烷或二甲醚之类的推进剂。
在本发明的剂型为溶液或乳浊液的情况下,可以利用溶剂、溶解剂或乳浊化剂作为载体成分,例如有水、乙醇、异丙醇、碳酸乙酯、乙酸乙酯、苯甲醇、苯甲酸苄酯、丙二醇、1、3-丁二醇油、脂肪族甘油酯、聚乙二醇或山梨聚糖的脂肪酸酯。
在本发明的剂型为悬浮液的情况下,可以利用水、乙醇或丙二醇之类的液态稀释剂、乙氧基化异硬脂醇、聚氧乙烯山梨醇酯以及聚氧乙烯山梨聚糖酯之类的悬浮剂、微晶纤维素、偏氢氧化铝、膨润土、琼脂或黄芪胶等作为载体成分。
在本发明的剂型为含有表面活性剂的清洁剂的情况下,可以利用脂肪醇硫酸盐、脂肪醇醚硫酸盐、磺基琥珀酸单酯、依西酸盐、咪唑啉衍生物、甲基牛磺酸酯、肌氨酸盐、脂肪酸酰胺醚硫酸盐、烷基酰胺甜菜碱、脂肪醇、脂肪酸甘油酯、脂肪酸二乙醇酰胺、植物油、羊毛脂衍生物或乙氧基化甘油脂肪酸酯等作为载体成分。
另一方面,根据本发明的一实施例的组合物,在保持稳定度的范围内可以含有色素、防腐剂、金属离子螯合剂、香等。
脱发或皮肤炎症抑制方法
本发明还涉及一种脱发或皮肤炎症抑制方法。所述脱发或皮肤炎症抑制方法,包括将如上所述的用于抑制脱发或皮肤炎症的组合物,适用于患有脱发或皮肤炎症的对象的步骤。所述脱发或皮肤炎症抑制方法可能意指预防、改善和/或治疗脱发或皮肤炎症的方法。
此时,所述用于抑制脱发或皮肤炎症的组合物可以在皮肤上涂抹而适用,优选的是,可以在担心脱发现象或出现脱发现象的头皮或担心炎症或出现炎症的皮肤上进行涂抹而适用。在将所述组合物涂抹在脸部皮肤上的情况下,能够从柚子油珠的香气中得到身心的安定而对睡眠更加有利。
另外,所述用于抑制脱发或皮肤炎症的组合物可以每天一次,涂抹在头皮或皮肤上。在所述组合物中含有的穗花杉双黄酮(Amentoflavone);以及选自由柏子仁提取物、染料木素(Genistein)以及鹰嘴豆芽素A(Biochanin A)组成的组中的一种以上的成分的组合通过抑制前列腺素D2合成酶的活性,减少引起脱发的因素即前列腺素D2的生成而抑制脱发反应,并抑制皮肤上的炎症反应,从而能够有利于抑制脱发或皮肤炎症。
另外,所述用于抑制脱发或皮肤炎症的组合物,当在皮肤上按每天1次,涂抹3周至8周时,能够表现脱发或皮肤炎症抑制效果得到了更好的改善。所述用于抑制脱发或皮肤炎症的组合物,每天仅适用于皮肤1次,也能够表现出优异的脱发或皮肤炎症抑制效果,通常,持续使用3周以上,优选为3周至8周时,能够表现非常优异的脱发或皮肤炎症抑制效果。
另外,所述用于抑制脱发或皮肤炎症的组合物的1次用量根据患有脱发或皮肤炎症的对象的状态、睡眠障碍程度、涂抹面积以及组合物形态不同,但通常可以为25mg~150mg,并且可以在所述1次用量范围内进行适当地调节而涂抹。
发明的实施方式
以下,通过实施例将更详细地说明本发明。这些实施例是用于例示本发明,对于本领域中具有通常知识的人来说显而易见的是,本发明的范围不应被解释为通过这些实施例所限制。
<实施例>用于抑制脱发或皮肤炎症的组合物的制备
<实施例1至实施例3>
在1000ml的净化水中添加穗花杉双黄酮(Amentoflavone)与选自由柏子仁提取物、染料木素(Genistein)以及鹰嘴豆芽素A(Biochanin A)组成的组中的一种以上的成分之后进行搅拌。具体有效成分的含量示于下表1中。
<比较例1至比较例4>
比较例的组合物为单独使用在实施例1至实施例3中利用的相同有效成分,并以成分含量达到10倍进行制备。具体地,在1000ml的净化水中添加穗花杉双黄酮(Amentoflavone)、柏子仁提取物、染料木素(Genistain)以及鹰嘴豆芽素A(Biochan A)中的一种后进行搅拌。具体有效成分的含量如下表1所示。
[表1]
<试验例>前列腺素D2合成酶活性抑制效果(酶联免疫吸附试验方法)
向前列腺素D2合成酶处理酶反应的基质即前列腺素H2(PGH2)而生成前列腺素D2(PGD2),将通过实施例1至实施例3制成的组合物一起投入之后,测定前列腺素D2的生成减少量,由此确认前列腺素D2合成酶活性抑制效果。
所述前列腺素D2的生成量测定是通过酶联免疫吸附试验(Enzyme Linked ImmunoSorbent Assay;ELISA)方法进行测定。酶联免疫吸附试验(ELISA)的实施由以下步骤组成:
(a)将实施例1至实验例3涂抹于固体基质的表面上的步骤;
(b)将前列腺素D2合成酶与所述前列腺素H2进行反应的步骤;
(c)将所述步骤b的产物与结合有酶的二级抗体进行反应的步骤;以及
(d)通过使用酶标仪(ELISA reader)在410nm下测定吸光度来显示所述酶的活性的步骤。
适合用作所述固体基质的是碳氢聚合物(例如,聚乙烯以及聚丙烯)、玻璃、金属或凝胶,最优选为微量滴定板。与所述二级抗体结合的酶包含催化显色反应、荧光反应、发光反应或红外线反应的酶,但不限于此,例如,包含碱性磷酸酶、β-半乳糖苷酶、辣根过氧化物酶、荧光素酶以及细胞色素P450。在作为与所述二级抗体结合的酶利用碱性磷酸酶的情况下,作为基质可以利用5-溴-4-氯-3-吲哚基磷酸盐(BCIP)、硝基四氮唑蓝(NBT)、萘酚AS-BI磷酸盐(naphthol-AS-B1-Phosphate)以及ECF(enhanced chemiflorescence)之类的显色反应基质,在利用辣根过氧化物酶的情况下,可以利用氯萘酚、氨基乙基咔唑、二氨基联苯胺、D-荧光素、光泽精(双-N-甲基吖啶硝酸盐)、甲香豆素苄醚、鲁米诺、荧光红试剂(10-乙酰基-3,7-二羟基吩嗪)、3,3,5,5-四甲基联苯胺(3,3,5,5-tetramethylbenzidine,TMB)、2,2'-叠氮二[3-乙基苯并噻唑啉磺酸盐(2,2'-Azine-di[3-ethylbenzthiazolinesulfonate],ABTS)以及邻苯二胺(OPD)等基质。
分析结果,如图1所示,本发明的实施例1至实施例3与成分含量多10倍的比较例1至比较例4相比,显示前列腺素D2的生成量减少。因此,通过所述结果,本发明人可知组合有穗花杉双黄酮与选自由柏子仁提取物、染料木素以及鹰嘴豆芽素A组成的组中的一种以上的成分的组合物,与单独使用所述成分物质的情况相比,前列腺素D2合成酶活性抑制能力更优异。
以下对根据本发明的一实施例的组合物的剂型例进行说明,但除这些剂型例以外,还可以应用为各种剂型,这只是用于例示本发明,本发明的范围并不受这些剂型例的限定。
<剂型例1>片剂
将根据本发明的实施例1至实施例3制成的组合物100mg、乳糖400mg,玉米淀粉400mg以及硬脂酸镁2mg进行混合后,按照常规的片剂的制备方法进行压片而制备片剂。
<剂型例2>胶囊剂
将根据本发明的实施例1至实施例3制成的组合物100mg、乳糖400mg、玉米淀粉400mg以及硬脂酸镁2mg进行混合后,按照常规的胶囊剂的制备方法填充到明胶胶囊中而制备胶囊剂。
<剂型例3>颗粒剂
将根据本发明的实施例1至实施例3制成的组合物50mg、无水结晶葡萄糖250mg以及淀粉550mg进行混合,使用流化床造粒机成型为颗粒之后,填充到袋中。
<剂型例4>饮品剂
将根据本发明的实施例1至实施例3制成的组合物50mg、葡萄糖10g、枸橼酸0.6g以及液态低聚糖25g进行混合后,加入300ml的净化水并在每瓶中按200ml的量填充后,在130℃下杀菌4~5秒钟,制备饮品剂。
<剂型例5>注射剂
按照下表2中记载的组分,通过常规方法制备注射剂。
[表2]
调配成分 | 含量 |
根据实施例1至实施例3制成的组合物 | 10-50mg |
注射用灭菌蒸馏水 | 适量 |
pH调节剂 | 适量 |
<剂型例6>柔软化妆水(润肤液)
按照下表3中记载的组分,通过常规方法制备柔软化妆水。
[表3]
<剂型例7>营养化妆水(牛奶润肤露)
按照下表4中记载的组分,通过常规方法制备营养化妆水。
[表4]
调配成分 | 含量(重量%) |
根据实施例1至实施例3制成的组合物 | 1.0 |
甘油 | 3.0 |
丁二醇 | 3.0 |
丙二醇 | 3.0 |
羧乙烯聚合物 | 0.1 |
蜜蜡 | 4.0 |
聚山梨酯60 | 1.5 |
辛酸/癸酸甘油三酯 | 5.0 |
角鲨烷 | 5.0 |
倍半油酸山梨糖醇酯 | 1.5 |
液体石蜡 | 0.5 |
鲸蜡硬脂醇 | 1.0 |
三乙醇胺 | 0.2 |
防腐剂、色素、香料 | 适量 |
净化水 | 余量 |
<剂型例8>按摩霜
按照下表5中记载的组分,通过常规方法制备按摩霜。
[表5]
<剂型例9>洗发乳的制备
按照下表6中记载的组分,通过常规方法制备洗发乳。
[表6]
成分 | 含量(重量%) |
根据实施例1至实施例3制成的组合物 | 2.0 |
净化水 | 余量 |
甘油 | 3.0 |
丁二醇 | 3.0 |
液体石蜡 | 7.0 |
β-葡聚糖 | 7.0 |
卡波姆 | 0.1 |
雪绒花提取物 | 2.0 |
辛酸/癸酸甘油三酯 | 3.0 |
角鲨烷 | 5.0 |
鲸蜡硬脂基葡糖苷 | 1.5 |
山梨醇硬脂酸酯 | 0.4 |
聚山梨酯 | 1.2 |
防腐剂 | 适量 |
香料 | 适量 |
色素 | 适量 |
三乙醇胺 | 0.1 |
<剂型例10>洗发水组合物的制备
按照下表7中记载的组分,通过常规方法制备洗发水组合物。
[表7]
成分(重量%) | 含量(重量%) |
聚季铵盐-10 | 0.5 |
月桂醇聚醚硫酸钠 | 20 |
根据实施例1至实施例3制成的组合物 | 0.3 |
香料 | 1.0 |
羟苯甲酯 | 0.1 |
鲸蜡醇 | 0.5 |
氯化钠 | 0.8 |
净化水 | 至100 |
<剂型例11>发膜的制备
按照下表8中记载的组分,通过常规方法制备发膜。
[表8]
区分(重量%) | 含量(重量%) |
根据实施例1至实施例3制成的组合物 | 0.5 |
硬脂酰胺丙基二甲胺 | 2 |
甘油 | 0.5 |
香料 | 0.5 |
防腐剂 | 0.03 |
十八醇 | 5 |
乳酸 | 1 |
蒸馏水 | 至100 |
Claims (15)
1.一种用于抑制脱发或皮肤炎症的组合物,包含:穗花杉双黄酮(Am entoflavone);以及选自由柏子仁提取物、染料木素(Genistein)以及鹰嘴豆芽素A(Biochanin A)组成的组中的一种以上的成分。
2.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述穗花杉双黄酮(Amentoflavone)相对于所述组合物总重量,含有0.1ppm至1,000ppm。
3.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述穗花杉双黄酮(Amentoflavone)是从选自由佛手、卷柏、拳柏、扁柏以及银杏组成的组中的一种以上提取而成的。
4.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述柏子仁提取物相对于所述组合物总重量,含有10ppm至10,000ppm。
5.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述染料木素(Genistein)相对于所述组合物总重量,含有1ppm至1,000ppm。
6.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述染料木素(Genistein)是从选自由豆、异黄酮(Isoflavone)组成的组中的一种以上提取而成的。
7.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述鹰嘴豆芽素A(Biochanin A)相对于所述组合物总重量,含有10ppm至1,000ppm。
8.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述鹰嘴豆芽素A(Biochanin A)是从选自由降香、豆、红三叶以及异黄酮(Isoflavone)组成的组中的一种以上提取而成的。
9.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述组合物抑制体内前列腺素D2合成酶(Prostagladin D2 Synthase,PTGDS)的活性。
10.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述用于抑制脱发或皮肤炎症的组合物为化妆料。
11.根据权利要求10所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述化妆料的剂型选自溶液、面霜、乳液、洗发水、护发素、喷雾剂以及凝胶中。
12.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述用于抑制脱发或皮肤炎症的组合物通过经皮注射或皮下注射投入到人体中。
13.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述用于抑制脱发或皮肤炎症的组合物为皮肤外用制剂或口服给药制剂。
14.根据权利要求1所述的用于抑制脱发或皮肤炎症的组合物,其特征在于,
所述皮肤包括毛囊以及头皮。
15.一种脱发或皮肤炎症抑制方法,利用权利要求1至14中任一项所述的组合物。
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KR100755983B1 (ko) * | 2006-10-02 | 2007-09-06 | 주식회사 라이프투게더 | 대나무 추출물을 함유하는 발모 촉진 또는 탈모 방지용조성물 및 이의 제조 방법 |
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JP7441217B2 (ja) | 2024-02-29 |
KR20200064309A (ko) | 2020-06-08 |
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