CN117137829A - 一种油珠次抛精华液及其制备方法 - Google Patents
一种油珠次抛精华液及其制备方法 Download PDFInfo
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- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 claims abstract description 30
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Classifications
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
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- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
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- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
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Abstract
本发明涉及化妆品技术领域,且公开了一种油珠次抛精华液及其制备方法,由以下组分组成,水相:3‑8%甘油、2‑10%1,3丙二醇、0.01‑0.03%卡波姆、0.2‑0.3%丙烯酸类或C10‑30烷醇丙烯酸酯交联聚合物、3‑5%烟酰胺、0.05‑0.1%季铵盐接枝透明质酸、0.1‑0.5%对羟基苯乙酮、0.2‑0.5%1,2‑己二醇、0.06‑0.08%卡瓦胡椒根提取物、0.1‑0.4%氨甲基丙醇、0.01‑0.1%乙二胺四乙酸二钠、0.06‑0.2%二葡糖基棓酸;油相:4‑6%异壬酸异壬酯、0.5‑1.3%生育酚乙酸酯、0.3‑1.2%抗坏血酸四异棕榈酸酯、0.04‑1.1%野大豆油、0.05‑0.7%角鲨烷、0.01‑0.8%霍霍巴籽油、0.02‑0.05%灵芝孢子油提取物、0.06‑0.8%胡萝卜根提取物、0.07‑0.3%β‑胡萝卜素;本发明的油珠次抛精华液具有美白、抗紫外线、抗皱功效,同时携带和使用方便,生产成本低,工艺简单。
Description
技术领域
本发明涉及化妆品技术领域,具体为一种油珠次抛精华液及其制备方法。
背景技术
精华液有提拉紧致,保湿,祛皱,促进细胞再生的作用,让肌肤保持更好的状态,目前,常见的水、乳霜、面霜中营养分子因为成分体积相对较大,吸收效果和渗透能力不足,很难起到护肤的效果,次抛就是“一次一支一抛”,次抛一般是小软瓶进行包装,每支独立包装,体积小,携带和使用方便,皮肤衰老主要为自然衰老和光老化,自然衰老主要为遗传基因引起的,明显特征为皱纹和松弛,同时出现色素沉淀现象,光老化主要是自然衰老和紫外线共同作用的结果,皮肤粗糙无光和色素沉着加深,皮肤微循环变差,弹性组织变形,真皮厚度变薄,如专利CN105997828B公开了一种涂抹水光精华液,具有消炎抗敏、保湿滋润、美白淡斑、祛痘抗皱和修复肌肤等功效,但是携带不方便。
发明内容
(一)解决的技术问题
针对现有技术的不足,本发明提供了一种具有抗衰老、保湿、促进新陈代谢的油珠次抛精华液及其制备方法。
(二)技术方案
为实现上述目的,本发明提供以下技术方案:一种油珠次抛精华液,所述油珠次抛精华液包括组分水相和组分油相。
优选的,所述水相以质量分数计含有:3-8%甘油、2-10%1,3丙二醇、0.01-0.03%卡波姆、0.2-0.3%丙烯酸类或C10-30烷醇丙烯酸酯交联聚合物、3-5%烟酰胺、0.05-0.1%季铵盐接枝透明质酸、0.1-0.5%对羟基苯乙酮、0.2-0.5%1,2-己二醇、0.06-0.08%卡瓦胡椒根提取物、0.1-0.4%氨甲基丙醇、0.01-0.1%乙二胺四乙酸二钠、0.06-0.2%二葡糖基棓酸。
优选的,所述油相以质量分数计含有:4-6%异壬酸异壬酯、0.5-1.3%生育酚乙酸酯、0.3-1.2%抗坏血酸四异棕榈酸酯、0.04-1.1%野大豆油、0.05-0.7%角鲨烷、0.01-0.8%霍霍巴籽油、0.02-0.05%灵芝孢子油提取物、0.06-0.8%胡萝卜根提取物、0.07-0.3%β-胡萝卜素。
优选的,所述季铵盐接枝透明质酸的制备方法为:将2-3g透明质酸、39.27-41.35g异丙醇、6-8g2-羟基-3-(辛酰氧基)丙基-2-(三甲铵基)乙基磷酸酯加入反应器中,水浴加热至70-80℃搅拌反应12-14min,冷却后过滤,依次用甲醇、丙酮洗涤70-90℃烘箱中烘干,得到季铵盐接枝透明质酸。
优选的,所述灵芝孢子油提取物中各个组分及其占油珠次抛精华液总质量的百分比为:三萜类0.02-0.13%、脂肪酸类0.001-0.009%、醇类0.08-0.21%、油脂类0.01-0.31%。
优选的,所述灵芝孢子油提取物的制备方法为:取经过60-70目分子筛的灵芝孢子粉0.5-0.7g加入反应器中,在向其加入溶剂,放入微波提取器中,微波功率400-500W,反应温度55-60℃,提取4-6min后吸取上清液得到灵芝孢子油提取物。
优选的,所述加入溶剂为:质量比为1:3.55-3.57的四丁基氯化铵、癸酸。
优选的,所述油珠次抛精华液的制备方法为:
(1)将去离子水、卡波姆、丙烯酸类或C10-30烷醇丙烯酸酯交联聚合物加入真空乳化锅中分散,再加入甘油、烟酰胺、季铵盐接枝透明质酸、乙二胺四乙酸二钠,搅拌升温至80-85℃,搅拌均匀至无颗粒呈均匀液体,降温至50-60℃,加入预溶好的1,3-丙二醇、对羟基苯乙酮、1,2-己二醇,继续降温至40-45℃,加入卡瓦胡椒根提取物、二葡糖基棓酸和0.1-0.2%氨甲基丙醇,得到水相;
(2)将异壬酸异壬酯、生育酚乙酸酯、抗坏血酸四异棕榈酸酯、野大豆油、角鲨烷、霍霍巴籽油、胡萝卜根提取物、灵芝孢子油提取物、β-胡萝卜素、生育酚混合,并搅拌0.5-2h得到油相,备用;
(3)在搅拌状态下将所述(2)中油相加入到乳化锅中,搅拌0.5-3h形成悬浮油珠,将0.1-0.2%氨甲基丙醇加入去离子水中预分散,再加入至所述乳化锅中搅拌0.5-4h,将悬浮油珠分散均匀,停止搅拌,送检合格后出料;
(4)采用无菌灌装技术,对塑料进行吹瓶成型,将(3)中的悬浮油珠灌装到瓶中,灌装量为1.0-1.6mL,将灌装好的塑料瓶进行封口,得到油珠次抛精华液。
优选的,所述水相稠度为1000-5500mpa.s。
(三)有益的技术效果
本发明通过将季铵盐接枝透明质酸起到对皮肤美白保湿、去除角质、改善皮肤毛孔粗大和修复角质损伤的作用,其中的磷脂基团对皮肤起到保湿、抗氧化、减少油脂分泌的作用;季铵盐会吸附到菌体表面,疏水基插入类脂层,破坏细胞膜通透性影响细胞的代谢过程,导致菌体死亡;瓦胡椒根提取物和灵芝孢子油提取物协同作用促进角质细胞的增生,加快新陈代谢使皮肤更润滑;本发明的透明质酸能够形成保护膜增强肌肤的防护功能,同时具有保湿的功效;1,2-己二醇、1,3丙二醇起到抑菌保湿的作用,较好的保护皮肤;对羟基苯乙酮可以起到防腐的作用;乙二胺四乙酸二钠抑制细菌生长所需的金属离子,起到保护皮肤的作用。
附图说明
图1是季铵盐接枝透明质酸反应线路图。
具体实施方式
实施例1
(1)将2g透明质酸、39.27g异丙醇、6g2-羟基-3-(辛酰氧基)丙基-2-(三甲铵基)乙基磷酸酯加入反应器中,水浴加热至70℃搅拌反应12min,冷却后过滤,依次用甲醇、丙酮洗涤70℃烘箱中烘干,得到季铵盐接枝透明质酸;
(2)灵芝孢子油提取物的制备方法为:取经过60目分子筛的灵芝孢子粉0.5g加入反应器中,在向其加入质量比为1:3.55的四丁基氯化铵、癸酸,放入微波提取器中,微波功率400W,反应温度55℃,提取4min后吸取上清液得到灵芝孢子油提取物;所述灵芝孢子油提取物中各个组分及其占油珠次抛精华液总质量的百分比为:三萜类0.02%、脂肪酸类0.001%、醇类0.08%、油脂类0.01%;
(3)将去离子水、0.01%卡波姆、0.2%丙烯酸类或C10-30烷醇丙烯酸酯交联聚合物加入真空乳化锅中分散,再加入6%甘油、3%烟酰胺、0.05%季铵盐接枝透明质酸、0.01%乙二胺四乙酸二钠,搅拌升温至80℃,搅拌均匀至无颗粒呈均匀液体,降温至50℃,加入预溶好的5%1,3-丙二醇、0.1%对羟基苯乙酮、0.2%1,2-己二醇,继续降温至40℃,加入0.06%卡瓦胡椒根提取物、0.06%二葡糖基棓酸和0.1%氨甲基丙醇,得到水相,稠度为1000mpa.s;
(4)将4%异壬酸异壬酯、0.5%生育酚乙酸酯、0.3%抗坏血酸四异棕榈酸酯、0.04%野大豆油、0.05%角鲨烷、0.01%霍霍巴籽油、0.06%胡萝卜根提取物、0.02%灵芝孢子油提取物、0.07%β-胡萝卜素混合,并搅拌1h得到油相,备用;
(5)在搅拌状态下将所述(2)中油相加入到乳化锅中,搅拌2h形成悬浮油珠,将0.1%氨甲基丙醇加入去离子水中预分散,再加入至所述乳化锅中搅拌2h,将悬浮油珠分散均匀,停止搅拌,送检合格后出料;
(6)采用无菌灌装技术,对塑料进行吹瓶成型,将(3)中的悬浮油珠灌装到瓶中,灌装量为1.2mL,将灌装好的塑料瓶进行封口,得到油珠次抛精华液。
实施例2
(1)将3g透明质酸、41.35g异丙醇、8g2-羟基-3-(辛酰氧基)丙基-2-(三甲铵基)乙基磷酸酯加入反应器中,水浴加热至80℃搅拌反应14min,冷却后过滤,依次用甲醇、丙酮洗涤90℃烘箱中烘干,得到季铵盐接枝透明质酸;
(2)灵芝孢子油提取物的制备方法为:取经过70目分子筛的灵芝孢子粉0.7g加入反应器中,在向其加入质量比为1: 3.57的四丁基氯化铵、癸酸,放入微波提取器中,微波功率500W,反应温度60℃,提取6min后吸取上清液得到灵芝孢子油提取物;所述灵芝孢子油提取物中各个组分及其占油珠次抛精华液总质量的百分比为:三萜类0.13%、脂肪酸类0.009%、醇类0.21%、油脂类0.31%;
(3)将去离子水、0.03%卡波姆、0.3%丙烯酸类或C10-30烷醇丙烯酸酯交联聚合物加入真空乳化锅中分散,再加入8%甘油、5%烟酰胺、0.1%季铵盐接枝透明质酸、0.1%乙二胺四乙酸二钠,搅拌升温至80℃,搅拌均匀至无颗粒呈均匀液体,降温至60℃,加入预溶好的10%1,3-丙二醇、0.5%对羟基苯乙酮、0.5%1,2-己二醇,继续降温至45℃,加入0.08%卡瓦胡椒根提取物、0.2%二葡糖基棓酸和0.2%氨甲基丙醇,得到水相,稠度为2500mpa.s;
(4)将6%异壬酸异壬酯、1.3%生育酚乙酸酯、1.2%抗坏血酸四异棕榈酸酯、1.1%野大豆油、0.7%角鲨烷、0.8%霍霍巴籽油、0.8%胡萝卜根提取物、0.05%灵芝孢子油提取物、0.3%β-胡萝卜素混合,并搅拌2h得到油相,备用;
(5)在搅拌状态下将所述(2)中油相加入到乳化锅中,搅拌3h形成悬浮油珠,将0.2%氨甲基丙醇加入去离子水中预分散,再加入至所述乳化锅中搅拌4h,将悬浮油珠分散均匀,停止搅拌,送检合格后出料;
(6)采用无菌灌装技术,对塑料进行吹瓶成型,将(3)中的悬浮油珠灌装到瓶中,灌装量为1.6mL,将灌装好的塑料瓶进行封口,得到油珠次抛精华液。
实施例3
(1)将2.5g透明质酸、40.31g异丙醇、7g2-羟基-3-(辛酰氧基)丙基-2-(三甲铵基)乙基磷酸酯加入反应器中,水浴加热至75℃搅拌反应13min,冷却后过滤,依次用甲醇、丙酮洗涤80℃烘箱中烘干,得到季铵盐接枝透明质酸;
(2)灵芝孢子油提取物的制备方法为:取经过65目分子筛的灵芝孢子粉0.6g加入反应器中,在向其加入质量比为1:3.56的四丁基氯化铵、癸酸,放入微波提取器中,微波功率450W,反应温度57.5℃,提取5min后吸取上清液得到灵芝孢子油提取物;所述灵芝孢子油提取物中各个组分及其占油珠次抛精华液总质量的百分比为:三萜类0.075%、脂肪酸类0.005%、醇类0.145%、油脂类0.16%;
(3)将去离子水、0.02%卡波姆、0.25%丙烯酸类或C10-30烷醇丙烯酸酯交联聚合物加入真空乳化锅中分散,再加入7%甘油、4%烟酰胺、0.075%季铵盐接枝透明质酸、0.055%乙二胺四乙酸二钠,搅拌升温至85℃,搅拌均匀至无颗粒呈均匀液体,降温至55℃,加入预溶好的7.5%1,3-丙二醇、0.3%对羟基苯乙酮、0.35%1,2-己二醇,继续降温至42.5℃,加入0.07%卡瓦胡椒根提取物、0.13%二葡糖基棓酸和0.15%氨甲基丙醇,得到水相,稠度为1750mpa.s;
(4)将5%异壬酸异壬酯、0.9%生育酚乙酸酯、0.75%抗坏血酸四异棕榈酸酯、0.57%野大豆油、0.375%角鲨烷、0.405%霍霍巴籽油、0.43%胡萝卜根提取物、0.035%灵芝孢子油提取物、0.185%β-胡萝卜素混合,并搅拌1.5h得到油相,备用;
(5)在搅拌状态下将所述(2)中油相加入到乳化锅中,搅拌2.5h形成悬浮油珠,将0.15%氨甲基丙醇加入去离子水中预分散,再加入至所述乳化锅中搅拌3h,将悬浮油珠分散均匀,停止搅拌,送检合格后出料;
(6)采用无菌灌装技术,对塑料进行吹瓶成型,将(3)中的悬浮油珠灌装到瓶中,灌装量为1.4mL,将灌装好的塑料瓶进行封口,得到油珠次抛精华液。
实施例4
(1)将2g透明质酸、39.27g异丙醇、6g2-羟基-3-(辛酰氧基)丙基-2-(三甲铵基)乙基磷酸酯加入反应器中,水浴加热至70℃搅拌反应12min,冷却后过滤,依次用甲醇、丙酮洗涤70℃烘箱中烘干,得到季铵盐接枝透明质酸;
(2)灵芝孢子油提取物的制备方法为:取经过60目分子筛的灵芝孢子粉0.5g加入反应器中,在向其加入质量比为1:3.55的四丁基氯化铵、癸酸,放入微波提取器中,微波功率400W,反应温度55℃,提取4min后吸取上清液得到灵芝孢子油提取物;所述灵芝孢子油提取物中各个组分及其占油珠次抛精华液总质量的百分比为:三萜类0.02%、脂肪酸类0.001%、醇类0.08%、油脂类0.01%;
(3)将去离子水、0.03%卡波姆、0.3%丙烯酸类或C10-30烷醇丙烯酸酯交联聚合物加入真空乳化锅中分散,再加入8%甘油、5%烟酰胺、0.1%季铵盐接枝透明质酸、0.1%乙二胺四乙酸二钠,搅拌升温至80℃,搅拌均匀至无颗粒呈均匀液体,降温至60℃,加入预溶好的10%1,3-丙二醇、0.5%对羟基苯乙酮、0.5%1,2-己二醇,继续降温至45℃,加入0.08%卡瓦胡椒根提取物、0.2%二葡糖基棓酸和0.2%氨甲基丙醇,得到水相,稠度为2500mpa.s;
(4)将6%异壬酸异壬酯、1.3%生育酚乙酸酯、1.2%抗坏血酸四异棕榈酸酯、1.1%野大豆油、0.7%角鲨烷、0.8%霍霍巴籽油、0.8%胡萝卜根提取物、0.05%灵芝孢子油提取物、0.3%β-胡萝卜素混合,并搅拌2h得到油相,备用;
(5)在搅拌状态下将所述(2)中油相加入到乳化锅中,搅拌2.5h形成悬浮油珠,将0.2%氨甲基丙醇加入去离子水中预分散,再加入至所述乳化锅中搅拌3h,将悬浮油珠分散均匀,停止搅拌,送检合格后出料;
(6)采用无菌灌装技术,对塑料进行吹瓶成型,将(3)中的悬浮油珠灌装到瓶中,灌装量为1.4mL,将灌装好的塑料瓶进行封口,得到油珠次抛精华液。
实施例5
(1)将3g透明质酸、41.35g异丙醇、8g2-羟基-3-(辛酰氧基)丙基-2-(三甲铵基)乙基磷酸酯加入反应器中,水浴加热至80℃搅拌反应14min,冷却后过滤,依次用甲醇、丙酮洗涤90℃烘箱中烘干,得到季铵盐接枝透明质酸;
(2)灵芝孢子油提取物的制备方法为:取经过70目分子筛的灵芝孢子粉0.7g加入反应器中,在向其加入质量比为1: 3.57的四丁基氯化铵、癸酸,放入微波提取器中,微波功率500W,反应温度60℃,提取6min后吸取上清液得到灵芝孢子油提取物;所述灵芝孢子油提取物中各个组分及其占油珠次抛精华液总质量的百分比为:三萜类0.13%、脂肪酸类0.009%、醇类0.21%、油脂类0.31%;
(3)将去离子水、0.02%卡波姆、0.25%丙烯酸类或C10-30烷醇丙烯酸酯交联聚合物加入真空乳化锅中分散,再加入7%甘油、4%烟酰胺、0.075%季铵盐接枝透明质酸、0.055%乙二胺四乙酸二钠,搅拌升温至85℃,搅拌均匀至无颗粒呈均匀液体,降温至55℃,加入预溶好的7.5%1,3-丙二醇、0.3%对羟基苯乙酮、0.35%1,2-己二醇,继续降温至42.5℃,加入0.07%卡瓦胡椒根提取物、0.13%二葡糖基棓酸和0.1%氨甲基丙醇,得到水相,稠度为1750mpa.s;
(4)将5%异壬酸异壬酯、0.9%生育酚乙酸酯、0.75%抗坏血酸四异棕榈酸酯、0.57%野大豆油、0.375%角鲨烷、0.405%霍霍巴籽油、0.43%胡萝卜根提取物、0.035%灵芝孢子油提取物、0.185%β-胡萝卜素混合,并搅拌1.5h得到油相,备用;
(5)在搅拌状态下将所述(2)中油相加入到乳化锅中,搅拌2h形成悬浮油珠,将0.1%氨甲基丙醇加入去离子水中预分散,再加入至所述乳化锅中搅拌2h,将悬浮油珠分散均匀,停止搅拌,送检合格后出料;
(6)采用无菌灌装技术,对塑料进行吹瓶成型,将(3)中的悬浮油珠灌装到瓶中,灌装量为1.2mL,将灌装好的塑料瓶进行封口,得到油珠次抛精华液。
对比例1
(1)灵芝孢子油提取物的制备方法为:取经过65目分子筛的灵芝孢子粉0.6g加入反应器中,在向其加入质量比为1:3.56的四丁基氯化铵、癸酸,放入微波提取器中,微波功率450W,反应温度57.5℃,提取5min后吸取上清液得到灵芝孢子油提取物;所述灵芝孢子油提取物中各个组分及其占油珠次抛精华液总质量的百分比为:三萜类0.075%、脂肪酸类0.005%、醇类0.145%、油脂类0.16%;
(2)将去离子水、0.03%卡波姆、0.3%丙烯酸类或C10-30烷醇丙烯酸酯交联聚合物加入真空乳化锅中分散,再加入8%甘油、5%烟酰胺、0.1%季铵盐接枝透明质酸、0.1%乙二胺四乙酸二钠,搅拌升温至80℃,搅拌均匀至无颗粒呈均匀液体,降温至60℃,加入预溶好的10%1,3-丙二醇、0.5%对羟基苯乙酮、0.5%1,2-己二醇,继续降温至45℃,加入0.08%卡瓦胡椒根提取物、0.2%二葡糖基棓酸和0.15%氨甲基丙醇,得到水相,稠度为2500mpa.s;
(3)将6%异壬酸异壬酯、1.3%生育酚乙酸酯、1.2%抗坏血酸四异棕榈酸酯、1.1%野大豆油、0.7%角鲨烷、0.8%霍霍巴籽油、0.8%胡萝卜根提取物、0.05%灵芝孢子油提取物、0.3%β-胡萝卜素,并搅拌2h得到油相,备用;
(4)在搅拌状态下将所述(2)中油相加入到乳化锅中,搅拌3h形成悬浮油珠,将0.15%氨甲基丙醇加入去离子水中预分散,再加入至所述乳化锅中搅拌4h,将悬浮油珠分散均匀,停止搅拌,送检合格后出料;
(5)采用无菌灌装技术,对塑料进行吹瓶成型,将(3)中的悬浮油珠灌装到瓶中,灌装量为1.6mL,将灌装好的塑料瓶进行封口,得到油珠次抛精华液。
实验例1
采用电容法测定人体皮肤角质层的水分含量是基于水和其他物质的介电常数差异显著,按照皮肤角质层水分含量的不同,测得的皮肤的电容值不同,其参数可代表皮肤水分含量。
随机选取100名20-40岁的试用者,分成6组,每组30名。6组试用者分别使用实施例1至实施例5和对比例1的油珠次抛精华液,每天早晚各使用一次,持续30天。
在第0天和第40天用皮肤含水量测试仪Corneometer CM825检测皮肤含水量,评估使用美白精华液前后皮肤的含水量情况。
保湿功效测试结果见表1。
表1
由表1可知使用本发明油抛次珠精华液的实施例1-5相较于对比例1,40天后皮肤的含水量显著提高。
实验例2
采用量化皮肤颜色的测量方法是由国际照明委员会(CIE)规定的色度系统(Lab色度系统)测量皮肤颜色的变化,该法量化比较准确,能反映皮肤颜色空间多维的变化,使肤色的量化更可靠。测试指标为皮肤白度L值(L值表征L*为白平衡,值越大,颜色越偏向白色)△L*=Tn-T0;式中Tn为受试区域随时间变化数值;T0为受试区域起始值。
筛选面部肤色较为暗淡的成年100名,随机分为6组,每组30名作为试用者,试用样品前对其面部皮肤进行黑色素和色差数据采集分析测试,数据作为皮肤本底值。试用者早晚各使用一次样品,连续使用5周。分别于第1周、第5周时进行数据采集。评测受试者使用化妆品前后皮肤白度的变化,从而确定化妆品的美白效果。
美白功效测试结果见表2
表2
由表2可以看出,在测试周期5周内,实施例1-5相较于对比例1受试者使用本发明油抛次珠精华液后提高了皮肤的白度。
以上公开的本发明优选实施例只是用于帮助阐述本发明。优选实施例并没有详尽叙述所有的细节,也不限制该发明仅为所述的具体实施方式。显然,根据本说明书的内容,可作很多的修改和变化。本说明书选取并具体描述这些实施例,是为了更好地解释本发明的原理和实际应用,从而使所属技术领域技术人员能很好地理解和利用本发明。本发明仅受权利要求书及其全部范围和等效物的限制。
Claims (7)
1.一种油珠次抛精华液,其特征在于,所述油珠次抛精华液包括组分水相和组分油相;
所述水相以质量分数计含有:3-8%甘油、2-10%1,3丙二醇、0.01-0.03%卡波姆、0.2-0.3%丙烯酸类或C10-30烷醇丙烯酸酯交联聚合物、3-5%烟酰胺、0.05-0.1%季铵盐接枝透明质酸、0.1-0.5%对羟基苯乙酮、0.2-0.5%1,2-己二醇、0.06-0.08%卡瓦胡椒根提取物、0.1-0.4%氨甲基丙醇、0.01-0.1%乙二胺四乙酸二钠、0.06-0.2%二葡糖基棓酸;
所述油相以质量分数计含有:4-6%异壬酸异壬酯、0.5-1.3%生育酚乙酸酯、0.3-1.2%抗坏血酸四异棕榈酸酯、0.04-1.1%野大豆油、0.05-0.7%角鲨烷、0.01-0.8%霍霍巴籽油、0.02-0.05%灵芝孢子油提取物、0.06-0.8%胡萝卜根提取物、0.07-0.3%β-胡萝卜素。
2.根据权利要求1所述的油珠次抛精华液,其特征在于,所述季铵盐接枝透明质酸的制备方法为:将2-3g透明质酸、39.27-41.35g异丙醇、6-8g2-羟基-3-(辛酰氧基)丙基-2-(三甲铵基)乙基磷酸酯加入反应器中,水浴加热至70-80℃搅拌反应12-14min,冷却后过滤,依次用甲醇、丙酮洗涤70-90℃烘箱中烘干,得到季铵盐接枝透明质酸。
3.根据权利要求1所述的油珠次抛精华液,其特征在于,所述灵芝孢子油提取物中各个组分及其占油珠次抛精华液总质量的百分比为:三萜类0.02-0.13%、脂肪酸类0.001-0.009%、醇类0.08-0.21%、油脂类0.01-0.31%。
4.根据权利要求3所述的油珠次抛精华液,其特征在于,所述灵芝孢子油提取物的制备方法为:取经过60-70目分子筛的灵芝孢子粉0.5-0.7g加入反应器中,在向其加入溶剂,放入微波提取器中,微波功率400-500W,反应温度55-60℃,提取4-6min后吸取上清液得到灵芝孢子油提取物。
5.根据权利要求4所述的油珠次抛精华液,其特征在于,所述加入溶剂为:质量比为1:3.55-3.57的四丁基氯化铵、癸酸。
6.根据权利要求1所述的油珠次抛精华液的制备方法,其特征在于,所述油珠次抛精华液的制备方法为:
(1)将去离子水、水相增稠卡波姆、丙烯酸类或C10-30烷醇丙烯酸酯交联聚合物加入真空乳化锅中分散,再加入甘油、烟酰胺、季铵盐接枝透明质酸、乙二胺四乙酸二钠,搅拌升温至80-85℃,搅拌均匀至无颗粒呈均匀液体,降温至50-60℃,加入预溶好的1,3-丙二醇、对羟基苯乙酮、1,2-己二醇,继续降温至40-45℃,加入卡瓦胡椒根提取物、二葡糖基棓酸和0.1-0.2%氨甲基丙醇,得到水相;
(2)将异壬酸异壬酯、生育酚乙酸酯、抗坏血酸四异棕榈酸酯、野大豆油、角鲨烷、霍霍巴籽油、胡萝卜根提取物、灵芝孢子油提取物、β-胡萝卜素、生育酚混合,并搅拌0.5-2h得到油相,备用;
(3)在搅拌状态下将所述(2)中油相加入到乳化锅中,搅拌0.5-3h形成悬浮油珠,将0.1-0.2%氨甲基丙醇加入去离子水中预分散,再加入至所述乳化锅中搅拌0.5-4h,将悬浮油珠分散均匀,停止搅拌,送检合格后出料;
(4)采用无菌灌装技术,对塑料进行吹瓶成型,将(3)中的悬浮油珠灌装到瓶中,灌装量为1.0-1.6mL,将灌装好的塑料瓶进行封口,得到油珠次抛精华液。
7.根据权利要求6所述的油珠次抛精华液的制备方法,其特征在于,所述(1)中水相稠度为1000-5500mpa.s。
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