CN112569151B - 一种抗敏修护屏障组合物及其制备方法和应用 - Google Patents
一种抗敏修护屏障组合物及其制备方法和应用 Download PDFInfo
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Abstract
本发明公开了一种抗敏修护屏障组合物及其制备方法和应用。按重量百分比计,该抗敏修护屏障组合物包含:寡肽‑1 0.1~20%;积雪草提取物0.1~50%;凤凰单丛茶茶叶挥发油0.1~30%;反式‑4‑叔丁基环己醇0.1~20%;神经酰胺2脂质体0.1~20%;低分子量透明质酸钠0.1~10%;高分子量透明质酸钠0.1~10%;尿素0.1~10%;去离子水余量。本发明在上百种原料中选取合适的原料,经过多种原料的科学配比,上百次功效验证实验后证明,寡肽‑1、积雪草提取物、凤凰单丛茶茶叶挥发油、反式‑4‑叔丁基己醇、神经酰胺2、透明质酸钠、尿素等组合后能达到舒缓皮肤敏感状态,修护皮肤屏障,抗炎等功效。
Description
技术领域
本发明涉及一种抗敏修护组合物,属于护肤品技术领域,特别是涉及一种抗敏修护屏障组合物及其制备方法和应用。
背景技术
敏感性皮肤(Sensitive Skin SS)是一种反应性高、耐受性差、较易过敏的皮肤,即对多种因素易感而诱发的主观感觉症状的皮肤情况。敏感性皮肤的成因较为复杂,目前行业内被普遍接受的成因有三种,一是皮肤的屏障受损;二是皮肤的神经反应增强;三是炎症反应。敏感性皮肤是一种皮肤的状态,主要特点是更为干燥、容易紧绷和发红;受到刺激会产生脱屑、瘙痒、灼热、刺痛等感受。
随着环境的污染加剧,人们生活工作的压力加大,对五花八门化妆品不假思索的随意使用,导致了敏感性皮肤的比例越来越多。有研究数据表明,在18~25岁的青年之中,敏感性肌肤发生率为31%,且女性的比例更高。
目前,市面上并没有能有效达到抗敏作用及修护皮肤屏障的化妆品,受到敏感性皮肤症状困扰的人们迫切需要可以解决这个问题的产品。
发明内容
本发明的目的是提供一种抗敏修护屏障组合物及其制备方法,组合后能达到舒缓皮肤敏感状态,修护皮肤屏障,抗炎等护肤功效。
本发明的另一目的是提供一种上述抗敏修护屏障组合物的应用,其可以应用到各种护肤剂型中,起到缓皮肤敏感状态,修护皮肤屏障,抗炎等护肤功效。
本发明的目的及解决其技术问题是采用以下技术方案来实现的。依据本发明提出的一种抗敏修护屏障组合物,按重量百分比计,是由如下原料制成:
进一步而言,上述抗敏修护屏障组合物,按重量百分比计,是由如下原料制成:
进一步而言,所述积雪草提取物是通过以下工艺制得的:
1)粉碎过筛:将干积雪草用破壁机粉碎,过50~200目筛;
2)提取:取积雪草50g,加入10~30倍体积水,在温度60~80℃下提取1~2h,重复提取3次,合并提取液;
3)浓缩过滤:对提取液过滤除去滤渣,并进行浓缩处理;
4)吸附洗脱:将浓缩液用D101B大孔树脂进行吸附,用50%乙醇进行洗脱1~3次,合并解脱液,进行减压浓缩将乙醇分离,得积雪草浸膏。
进一步而言,所述凤凰单丛茶茶叶挥发油是通过以下工艺制得的:
1)水蒸气蒸馏:将凤凰单丛茶茶叶置于水蒸气蒸馏发生器内,进行茶叶挥发油的蒸馏提取;
2)分离:将制得的茶叶挥发油和水的混合物进行分离,得凤凰单丛茶茶叶挥发油。
优选地,上述抗敏修护屏障组合物的制备方法,是由以下工艺制得:
将寡肽-1、积雪草提取物、凤凰单丛茶茶叶挥发油、反式-4-叔丁基环己醇、神经酰胺2脂质体、低分子量透明质酸钠、高分子量透明质酸钠、尿素、去离子水按照比例混合,搅拌均匀。
另外,本发明还公开了上述抗敏修护屏障组合物在护肤品中的应用,按重量百分比计,所述抗敏修护屏障组合物占护肤品总量的0.1%~10%;及90~99.9%的常规辅料。
进一步而言,上述抗敏修护屏障组合物在护肤品中的应用,按重量百分比计,所述抗敏修护屏障组合物占护肤品总量的0.5%~5%。
进一步而言,上述抗敏修护屏障组合物在护肤品中的应用,所述常规辅料包括表面活性剂、增稠剂、调理剂、保湿剂、防腐剂、螯合剂、香精、去离子水。
进一步而言,上述抗敏修护屏障组合物在护肤品中的应用,所述护肤品可制成爽肤水、柔肤水、紧肤水、营养化妆水、营养霜、按摩霜、精华、眼霜、眼部精华、洁肤霜、洁肤泡沫、洁肤水、面膜、粉饼、体露、体霜、体油、身体乳和体精华的各种剂型。
借由上述技术方案,本发明具有如下优点和有益效果:
1)本发明在上百种原料中选取合适的原料,经过多种原料的科学配比,上百次功效验证实验后证明,寡肽-1,积雪草提取物,凤凰单丛茶茶叶挥发油,反式-4-叔丁基环己醇,神经酰胺2,透明质酸钠(低分子量、高分子量),尿素等组合后能达到舒缓皮肤敏感状态,修护皮肤屏障,抗炎等功效;
2)寡肽-1和积雪草提取物可以促进角质层适度增殖,修护受损细胞,达到修护皮肤屏障的效果;
3)神经酰胺2、透明质酸钠(低分子量、高分子量),尿素,尿囊素组合可以达到最优的保湿效果,提高皮肤含水量从而牢固皮肤屏障;
4)凤凰单丛茶茶叶挥发油中的活性成分可以达到杀菌抑菌作用,抑制机体炎症因子的表达,从而起到抗炎效果;
5)反式-4-叔丁基环己醇能降低神经敏感性,起到镇静舒缓作用。
附图说明
图1是本发明实施例的含屏障修护组合物与与空白和市售产品的保湿效果对比图。
图2是实施例2抗敏测试效果图。
具体实施方式
以下通过具体较佳实施例结合效果试验例,对本发明作进一步详细说明,但本发明并不仅限于以下的实施例。
按重量百分比计,本发明的抗敏修护屏障组合物包含:寡肽-1 0.1~20%;积雪草提取物0.1~50%;凤凰单丛茶茶叶挥发油0.1~30%;反式-4-叔丁基环己醇0.1~20%;神经酰胺2脂质体0.1~20%;低分子量透明质酸钠0.1~10%;高分子量透明质酸钠0.1~10%;尿素0.1~10%;去离子水余量。
上述的原料组分分别介绍如下:
①寡肽-1:
甘氨酸、组氨酸和赖氨酸组成的多肽聚合物,能够促进细胞增殖分化,使皮肤光滑细嫩,强化皮肤屏障,加快皮肤修复过程,增加细胞间质,保持皮肤水分,减少皮肤水分流失;
②积雪草提取物:
伞形科雷公根属植物积雪草全草提取物,含有积雪草甙、参枯尼甙、异参枯尼甙、羟基积雪草甙等多种物质及胡萝卜烃类、叶绿素、槲皮素和葡萄糖的黄酮甙。可促进体内胶原合成和心血管生成,刺激肉芽生长等功效,故能促进伤口愈合,促进新陈代谢作用。
③凤凰单丛茶茶叶挥发油:
产自广东潮州凤凰山上的凤凰单枞茶,取其新鲜茶叶进行植物挥发油提取,经试验有抗炎活性。
④反式-4-叔丁基环己醇:
人工合成,能抑制香草酸亚型瞬时受体电位1通道蛋白(Transient receptorpotential vanilloid 1,TRPV-1)过表达,降低神经敏感度,达到舒缓镇静的效果。
⑤神经酰胺2脂质体:
神经酰胺是细胞间基质的主要部分,在保持角质层水分的平衡中起着重要作用,神经酰胺具有很强缔合水分子能力,它通过在角质层中形成网状结构维持皮肤水分。
⑥透明质酸钠(高分子量、小分子量):
天然保湿因子;大分子量(150~180万道尔顿)的透明质酸钠保湿效果更好;小分子量(1000~2000道尔顿)的透明质酸钠可渗入皮肤表皮层,促进皮肤营养的供给和废物的排泄,从而防止皮肤老化,起到美容和养颜作用;
⑦尿素:保湿剂。
其中,积雪草提取物的制备工艺可表述如下:
1)粉碎过筛:将干积雪草用破壁机粉碎,过50~200目筛;
2)提取:取积雪草50g,加入10~30倍体积水,在温度60~80℃下提取1~2H,重复提取3次,合并提取液;
3)浓缩过滤:对提取液过滤除去滤渣,并进行浓缩处理;
4)吸附洗脱:将浓缩液用D101B大孔树脂进行吸附,用50%乙醇进行洗脱1~3次,合并解脱液,进行减压浓缩将乙醇分离,得积雪草浸膏。
其中,凤凰单丛茶茶叶挥发油制备工艺可表述如下:
1)水蒸气蒸馏:将凤凰单丛茶茶叶置于水蒸气蒸馏发生器内,进行茶叶挥发油的蒸馏提取;
2)分离:将制得的茶叶挥发油和水的混合物进行分离,得凤凰单丛茶茶叶挥发油。
实施例1-3
一种抗敏修护屏障组合物,其原料组份如下表1所示。
表1抗敏修护屏障组合物的配方组份(重量百分比%)
原料组份 | 实施例1 | 实施例2 | 实施例3 |
寡肽-1 | 10% | 0.1% | 20% |
积雪草提取物 | 20% | 0.1% | 50% |
凤凰单丛茶茶叶挥发油 | 20% | 0.1% | 30% |
反式-4-叔丁基环己醇 | 4% | 20% | 0.1% |
神经酰胺2脂质体 | 4% | 20% | 0.1% |
低分子量透明质酸钠 | 5% | 0.1% | 10% |
高分子量透明质酸钠 | 5% | 10% | 0.1% |
尿素 | 5% | 10% | 0.1% |
去离子水 | 余量 | 余量 | 余量 |
上述实施例1-3的抗敏修护屏障组合物的制备工艺如下:
将寡肽-1、积雪草提取物、凤凰单丛茶茶叶挥发油、反式-4-叔丁基环己醇、神经酰胺2脂质体、低分子量透明质酸钠、高分子量透明质酸钠、尿素、去离子水按照比例混合,搅拌均匀。
以下实施例4-6为含有实施例1抗敏修护屏障组合物的外用护肤制品
实施例4(含抗敏修护屏障组合物的护肤凝胶)
一种含实施例1的抗敏修护屏障组合物的护肤凝胶,其配方原料如下表2所示。
表2含实施例1的抗敏修护屏障组合物的护肤凝胶的配方(重量百分比%)
上述实施例4的含抗敏修护屏障组合物的护肤凝胶的制备工艺如下:
1)先在去离子水中溶解增稠剂;
2)皮肤调理剂、防腐剂、去离子水溶解;
3)将两者混合搅拌;脱气;
4)加入pH调节剂、活性成分、香精、增溶剂等,在搅拌混合,脱气,出料。
实施例5(含抗敏修护屏障组合物的护肤水)
一种含实施例1的抗敏修护屏障组合物的护肤水,其配方原料如下表3所示。
表3含实施例1的抗敏修护屏障组合物的护肤水的配方(重量百分比%)
组分 | 原料 | 实施例5 |
活性成分 | 实施例1的抗敏修护屏障组合物 | 7% |
防腐剂 | 苯氧乙醇 | 0.1% |
芳香剂 | 日用香精 | 0.05% |
其他 | 去离子水 | 余量 |
上述实施例5的含抗敏修护屏障组合物的护肤水的制备工艺如下:
将所有成分加入去离子水中,搅拌混合,出料。
实施例6(含抗敏修护屏障组合物的护肤霜)
一种含实施例1的抗敏修护屏障组合物的护肤霜,其配方原料如下表4所示。
表4含实施例1的抗敏修护屏障组合物的护肤霜的配方(重量百分比%)
上述实施例6的含抗敏修护屏障组合物的护肤霜的制备工艺如下:
1)先加热到60℃在去离子水中溶解皮肤调理剂、增溶剂;
2)冷却至40℃以下加入活性成分、防腐剂、pH调节剂、增稠剂、防腐剂,混合搅拌,均质10min;
3)冷却出料。
以下为效果试验例的内容。
效果试验例
对比例1:
与实施例1相比,除了不含寡肽-1、积雪草提取物之外,包含凤凰单枞茶茶叶挥发油20%,反式-4-叔丁基环己醇5%,神经酰胺2脂质体5%,低分子量透明质酸钠6%,高分子量透明质酸钠6%,尿素6%,具体制备过程与实施例1相同;
对比例2:
与实施例1相比,除了不含寡肽-1之外,包含积雪草提取物20%,凤凰单枞茶茶叶挥发油25%,反式-4-叔丁基环己醇5%,神经酰胺2脂质体5%,低分子量透明质酸钠6%,高分子量透明质酸钠6%,尿素6%,具体制备过程与实施例1相同;
对比例3:
与实施例1相比,除了不含积雪草提取物之外,包含寡肽-1 10%,凤凰单枞茶茶叶挥发油10%,反式-4-叔丁基环己醇3%,神经酰胺2脂质体3%,低分子量透明质酸钠7%,高分子量透明质酸钠3%,尿素5%,具体制备过程与实施例1相同;
对比例4:
含寡肽-1 10%;
对比例5:
含积雪草提取物20%;
对比例6:
与实施例1相比,除了不含凤凰单枞茶茶叶挥发油之外,包含寡肽-1 10%,积雪草提取物10%,反式-4-叔丁基环己醇5%,神经酰胺2脂质体5%,低分子量透明质酸钠6%,高分子量透明质酸钠6%,尿素6%,具体制备过程与实施例1相同;
对比例7:
与实施例1相比,除了不含反式-4-叔丁基环己醇之外,包含寡肽-1 15%,雪草提取物15%,凤凰单枞茶茶叶挥发油10%,神经酰胺2脂质体5%,低分子量透明质酸钠6%,高分子量透明质酸钠6%,尿素6%,具体制备过程与实施例1相同;
对比例8:
与实施例1相比,除了不含神经酰胺2脂质体、低分子量透明质酸钠,高分子量透明质酸钠,尿素之外,包含寡肽-1 10%,积雪草提取物10%,反式-4-叔丁基环己醇6%,具体制备过程与实施例1相同;
对比例9:
与实施例1相比,除了不含神经酰胺2脂质体之外,包含寡肽-1 10%,积雪草提取物10%,反式-4-叔丁基环己醇6%,低分子量透明质酸钠10%,高分子量透明质酸钠10%,尿素10%,具体制备过程与实施例1相同;
对比例10:
与实施例1相比,除了不含低分子量透明质酸钠之外,包含寡肽-1 10%,积雪草提取物10%,反式-4-叔丁基环己醇6%,神经酰胺2脂质体10%,高分子量透明质酸钠10%,尿素10%,具体制备过程与实施例1相同;
对比例11:
与实施例1相比,除了不含高分子量透明质酸钠之外,包含寡肽-1 10%,积雪草提取物10%,反式-4-叔丁基环己醇6%,神经酰胺2脂质体10%,低分子量透明质酸钠10%,尿素10%,具体制备过程与实施例1相同;
对比例12:
与实施例1相比,除了不含尿素之外,包含寡肽-1 10%,积雪草提取物10%,反式-4-叔丁基环己醇6%,神经酰胺2脂质体10%,低分子量透明质酸钠10%,高分子量透明质酸钠10%,具体制备过程与实施例1相同。
效果评价1:HaCat-MTT抑制细胞毒性试验
MTT检测法原理:
活细胞线粒体中的琥珀酸脱氢酶能使外源性MTT还原为水不溶性的蓝紫色结晶甲瓒,而死细胞无此功能。二甲基亚砜(DMSO)能溶解细胞中的甲瓒,用酶标仪在490nm波长处测定其光吸收值,在一定细胞数范围内,MTT结晶形成的量与细胞数成正比。根据测得的吸光度值(OD值),来判断活细胞数量,OD值越大,细胞活性越强。
实验选用HaCat(永生化处理人角质形成细胞)细胞悬液浓度为3*105cell/ml,100μL/孔于96孔板内,于37℃,5%CO2进行培养。加入100μL/孔样品溶液PBS溶液(阴性对照)培养24H后,在加入60μg/mLSDS溶液培养24H(60μg/mLSDS存在下细胞活率为60%),后加入20μL/孔5mg/ml MTT溶液,置于培养箱反应4H后去除上清液,加入DMSO 150μL/孔,摇床震荡10min后,用酶联免疫检测仪测量490nm处吸光度。
在此实验中,吸光度值越大,证明样品使细胞免受SDS损伤的能力越强,表明样品修护能力越强。如下表5所示。
表5不同样品的浓度与OD值
由表5可得出以下结论:
1)对比例1、4~5和阴性对照相比可知:不含寡肽-1、积雪草提取物的对比例1的OD值与阴性对照接近;只含寡肽-1和只含积雪草提取物的对比例4~5的OD值明显高于阴性对照,说明寡肽-1、积雪草提取物具备使细胞免于SDS损伤的能力,具有修护受损细胞,达到修护皮肤屏障的效果;
2)实施例1~3对比例2~3对比可知,寡肽-1和积雪草提取物复配组合后,OD值明显增大,表明组合物修护细胞受损能力增强;且当含寡肽-1 10%、积雪草提取物20%时,修护能力最强,证明该比例为最佳比例。
效果评价2:抗炎试验和修护细胞屏障能力试验
抑制炎症因子(白介素IL-6)表达和促进血管内皮生长因子(VEGF)的表达。
炎症因子白介素IL-6可引起细胞内炎症产生。
血管内皮生长因子VEGF适当浓度下可促进HaCat的增殖,修护皮肤屏障。
选用HaCat细胞悬液浓度为3*105cell/ml,100μL/孔于6孔板内,于37℃,5%CO2进行培养至贴壁。加入3mL/孔样品溶液和SDS溶液的混合溶液,SDS溶液(阳性对照),PBS溶液(阴性对照)置于培养箱继续培养48H,取出后离心,去除沉淀。
用多重液相蛋白定量技术,采用具有特定荧光信号的微球链接特定的捕获抗体,再用于捕捉溶液中的不同的待检测物,根据荧光信号强度,对待检测物进行定量检测。表6所示为抑制炎症因子(白介素IL-6)的定量检测。
表6抑制炎症因子(白介素IL-6)的定量检测
由表6可以得出以下结论:
1)实施例1~3和对比例1~6可知,在凤凰单丛茶茶叶挥发油存在的测试样品IL-6含量较阳性对照低,证明凤凰单丛茶茶叶挥发油有抑制炎症因子产生的能力,具备有良好的抗炎效果;
2)实施例1~3和对比例1~3可知,缺少寡肽-1和积雪草提取物其中之一的样品IL-6含量较阴性对照高,但较阳性对照低,证明寡肽-1、积雪草提取物和凤凰单丛茶茶叶挥发油复配的情况下,可以发挥更优的抗炎效果。且当寡肽-1 10%,积雪草提取物20%,凤凰单丛茶茶叶挥发油20%时,效果最佳。
表7促进血管内皮生长因子(VEGF)的定量检测
样品 | 浓度 | VEGF(pg/mL) |
实施例1 | 0.1% | 153.52 |
实施例2 | 0.1% | 97.53 |
实施例3 | 0.1% | 84.45 |
对比例1 | 0.1% | 20.74 |
对比例2 | 0.1% | 30.12 |
对比例3 | 0.1% | 29.47 |
对比例6 | 0.1% | 21.25 |
对比例7 | 0.1% | 23.46 |
对比例8 | 0.1% | 30.67 |
对比例9 | 0.1% | 19.45 |
对比例10 | 0.1% | 24.00 |
对比例11 | 0.1% | 25.14 |
对比例12 | 0.1% | 34.45 |
SDS(阳性对照) | 60μg/ml | 24.23 |
PBS(阴性对照) | 10% | 51.58 |
由表7可得出以下结论:
1)实施例1~3和对比例1~11可知,缺少任一组分的样品VEGF的含量明显较阴性对照低,实施例1~3VEGF的含量明显高于阴性对照,证明抗敏修护屏障组合物有促进血管内皮生长因子(VEGF)的表达能力,具备良好的修护细胞屏障能力;
2)实施例1的VEGF含量明显高于实施例2~3,证明了屏障修护组合物配伍的合理性。
效果试验例3(人体保湿测试)
选取年龄在18~60周岁之间符合要求的受试者30名;用电容法皮肤水分测定仪预检,前臂测试区域基础值在15-45(Corneometer Unit,C.U.)之间。
测试过程中受试者需要恒温恒湿(温度:20℃-22℃,湿度:40%-60%)环境中,先用干净纸巾擦拭手臂内侧标记受试部位,静坐30min,测试空白值,按照(2.0±0.1mg)/cm2的量涂抹样品。
等待1h,2h,4h,8h后进行皮肤水分值测试。如图1和下表8所示。
表8人体保湿测试水分值(C.U)结果
样品 | 0H | 1H | 2H | 4H | 8H |
实施例4 | 32.5 | 60.1 | 59.2 | 57.2 | 45.7 |
实施例4水分变化率 | / | 84.9% | 82.2% | 76.0% | 40.61% |
市售竞品 | 33.1 | 52.1 | 45.1 | 40.3 | 35.1 |
市售竞品水分变化率 | / | 57.4% | 36.3% | 21.8% | 6.0% |
空白对照 | 30.1 | 31.2 | 33.4 | 29.8 | 32.3 |
空白水分变化率 | / | 3.7% | 11.0% | -1.0% | 7.3% |
由图1和表8的结果可知:
受试者在用了含屏障修护组合物的实施例4后,水分值明显比市售竞品和空白高,且与空白和市售产品相比均存在显著性差异,证明含有屏障修护组合物的实施例4具有保湿效果且保湿效果优于市售竞品,保湿效果较佳。
效果试验例4(人体抗敏测试)
样品为:实施例2和市面上口碑佳的保湿凝胶。
表9实施例2和市面上口碑佳的保湿凝胶的使用前后对比
由图2和表9的结果可知:
在使用样品1个月后,受试者红色区降低了46%,脸部皮肤敏感度下降。
以上所述,仅是本发明的较佳实施例而已,并非对本发明作任何形式上的限制,故凡是未脱离本发明技术方案内容,依据本发明的技术实质对以上实施例所作的任何简单修改、等同变化与修饰,均仍属于本发明技术方案的范围内。
Claims (9)
3.如权利要求1所述的抗敏修护屏障组合物,其特征在于:所述积雪草提取物是通过以下工艺制得的:
1)粉碎过筛:将干积雪草用破壁机粉碎,过50~200目筛;
2)提取:取积雪草50g,加入10~30倍体积水,在温度60~80℃下提取1~2h,重复提取3次,合并提取液;
3)浓缩过滤:对提取液过滤除去滤渣,并进行浓缩处理;
4)吸附洗脱:将浓缩液用D101B大孔树脂进行吸附,用50%乙醇进行洗脱1~3次,合并解脱液,进行减压浓缩将乙醇分离,得积雪草浸膏。
4.如权利要求1所述的抗敏修护屏障组合物,其特征在于:所述凤凰单丛茶茶叶挥发油是通过以下工艺制得的:
1)水蒸气蒸馏:将凤凰单丛茶茶叶置于水蒸气蒸馏发生器内,进行茶叶挥发油的蒸馏提取;
2)分离:将制得的茶叶挥发油和水的混合物进行分离,得凤凰单丛茶茶叶挥发油。
5.权利要求1-4中任一项所述的抗敏修护屏障组合物的制备方法,其特征在于:是由以下工艺制得:
将寡肽-1、积雪草提取物、凤凰单丛茶茶叶挥发油、反式-4-叔丁基环己醇、神经酰胺2脂质体、低分子量透明质酸钠、高分子量透明质酸钠、尿素、去离子水按照比例混合,搅拌均匀。
6.权利要求1-4中任一项所述的抗敏修护屏障组合物在护肤品中的应用,其特征在于:按重量百分比计,所述抗敏修护屏障组合物占护肤品总量的0.1%~10%;及90~99.9%的常规辅料。
7.根据权利要求6所述的抗敏修护屏障组合物在护肤品中的应用,其特征在于:按重量百分比计,所述抗敏修护屏障组合物占护肤品总量的0.5%~5%。
8.根据权利要求6所述的抗敏修护屏障组合物在护肤品中的应用,其特征在于:所述常规辅料包括表面活性剂、增稠剂、调理剂、保湿剂、防腐剂、螯合剂、香精、去离子水。
9.根据权利要求6所述的抗敏修护屏障组合物在护肤品中的应用,其特征在于:所述护肤品制成爽肤水、柔肤水、紧肤水、营养化妆水、营养霜、按摩霜、精华、眼霜、洁肤霜、洁肤泡沫、洁肤水、面膜、粉饼、体露、体油、身体乳的各种剂型。
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