CN113197814A - 一种玻尿酸微针贴片制备方法 - Google Patents
一种玻尿酸微针贴片制备方法 Download PDFInfo
- Publication number
- CN113197814A CN113197814A CN202110402936.7A CN202110402936A CN113197814A CN 113197814 A CN113197814 A CN 113197814A CN 202110402936 A CN202110402936 A CN 202110402936A CN 113197814 A CN113197814 A CN 113197814A
- Authority
- CN
- China
- Prior art keywords
- microneedle
- solution
- hyaluronic acid
- extract
- preparation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 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 title claims abstract description 46
- 229920002674 hyaluronan Polymers 0.000 title claims abstract description 46
- 229960003160 hyaluronic acid Drugs 0.000 title claims abstract description 46
- 238000002360 preparation method Methods 0.000 title claims abstract description 24
- 239000000243 solution Substances 0.000 claims abstract description 44
- 239000000284 extract Substances 0.000 claims abstract description 32
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 18
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- YDNKGFDKKRUKPY-JHOUSYSJSA-N C16 ceramide Natural products CCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)C=CCCCCCCCCCCCCC YDNKGFDKKRUKPY-JHOUSYSJSA-N 0.000 claims abstract description 13
- 102000008186 Collagen Human genes 0.000 claims abstract description 13
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- CRJGESKKUOMBCT-VQTJNVASSA-N N-acetylsphinganine Chemical compound CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)NC(C)=O CRJGESKKUOMBCT-VQTJNVASSA-N 0.000 claims abstract description 13
- 229940106189 ceramide Drugs 0.000 claims abstract description 13
- ZVEQCJWYRWKARO-UHFFFAOYSA-N ceramide Natural products CCCCCCCCCCCCCCC(O)C(=O)NC(CO)C(O)C=CCCC=C(C)CCCCCCCCC ZVEQCJWYRWKARO-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229920001436 collagen Polymers 0.000 claims abstract description 13
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 claims abstract description 13
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- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 8
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- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 claims description 2
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- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
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Classifications
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Landscapes
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- Cosmetics (AREA)
Abstract
本发明涉及一种玻尿酸微针贴片制备方法,包括以下原材料:微针溶液:透明质酸10‑15%、活性提取物5‑10%、神经酰胺3‑6%、水解胶原蛋白4‑8%、积雪草6‑12%、防腐剂0.5‑2%和去离子水60‑72%,基层原液:基质材料聚合物和去离子水,固液比为1:3,所述制备方法包括以下步骤:(1)微针溶液的制备:称取去离子水60‑72%,缓慢加入称量好的透明质酸10‑15%,待透明质酸完全溶胀后,加入活性提取物5‑10%、神经酰胺3‑6%、水解胶原蛋白4‑8%、积雪草6‑12%、防腐剂0.5‑2%,加热并提高搅拌速度直至溶液沸腾;(2)基层原液的制备:称取基质材料按照固液比为1:3加入去离子水,搅拌至溶解。本发明采用微针将天然活性成分送达皮肤内部,具有保湿、美白祛斑、延缓衰老、抗过敏、抗菌抗炎等功效。
Description
技术领域
本发明涉及护肤品技术领域,具体是指一种玻尿酸微针贴片制备方法。
背景技术
玻尿酸,又名透明质酸,是由葡糖醛酸和N-乙酰氨基葡糖为重复单位组成直链高分子多糖,是一种广泛存在于脊椎动物组织细胞外基质的生物大分子物质,在医药领域透明质酸又被称作玻璃酸,目前透明质酸的商品形式均为其钠盐。当玻尿酸涂于皮肤表面时,会形成一层具有黏弹性的透明水化膜,起到优良的保水功效,而且具有良好的透气性,无油腻感,令皮肤感觉自然,光滑透软。玻尿酸以其特有的保湿功效和理化兴性质,已成为国家上公认的优良天然保湿因子。
微针技术是一种新型的无痛微创给药系统,结合了透皮贴剂和注射剂型的优点,能够穿透皮肤角质层屏障,为大分子药物如蛋白质、疫苗等药物提供了新型的给药途径,克服了大分子药物的口服、透皮吸收问题。微针技术已逐渐成为医药领域、美容领域、微生物领域、精密制造领域的研究热点。
目前市面上的玻尿酸护肤产品种类繁多,但是大多数的产品作用仅停留在皮肤表层,护肤效果不够显著。金属微针皮肤穿透性高,但是对皮肤的创伤较大;硅微针有良好的传感性能和机电性能,但是硅微针容易断裂。因此,很有必要研发一种既能促进皮肤对玻尿酸的有效吸收,性能又十分良好的玻尿酸微针贴片。
发明内容
本发明的目的是提供一种玻尿酸微针贴片制备方法,以玻尿酸、神经酰胺、水解胶原蛋白等为主要成分,该产品具有保湿、抗皱、美白、抗炎等作用。
为解决上述技术问题,本发明提供的技术方案为:
一种玻尿酸微针贴片制备方法,包括以下原材料:微针溶液:透明质酸10-15%、活性提取物5-10%、神经酰胺3-6%、水解胶原蛋白4-8%、积雪草6-12%、防腐剂0.5-2%和去离子水60-72%,基层原液:基质材料聚合物和去离子水,固液比为1:3,所述制备方法包括以下步骤:
(1)微针溶液的制备:称取去离子水60-72%,在低速搅拌的条件下,缓慢加入称量好的透明质酸10-15%,待透明质酸完全溶胀后,加入活性提取物5-10%、神经酰胺3-6%、水解胶原蛋白4-8%、积雪草6-12%、防腐剂0.5-2%,加热并提高搅拌速度直至溶液沸腾,超声去除溶液中的气泡;
(2)基层原液的制备:称取基质材料按照固液比为1:3加入去离子水,搅拌至溶解,超声去除溶液中的气泡;
(3)模具的填充:取适量的微针溶液,倾倒于模具表面,均匀涂布后,使微针溶液进入并填满模具针状凹槽,将模具水平放置于真空干燥器内,打开真空泵,真空度为0.06-0.09MPa,连续抽真空1-1.5h,再加入基层原液,相同条件真空干燥;
(4)微针贴片的干燥:模具填充后,-80℃预冻1-2h,转入真空冷冻干燥机冻干24-36h;
(5)脱模:微针干燥至恒重后,缓慢剥离模具,即可得到微针贴片。
进一步的,所述防腐剂包括聚赖氨酸、苯甲酸、水杨酸或苯甲醇中的至少一种。
进一步的,所述活性提取物包括灵芝提取物、银耳提取物、芦荟提取物、红花提取物、丹参提取物、紫草根提取物、红景天提取物或乳香提取物中的至少一种。
进一步的,所述基质材料聚合物包括聚乳酸、聚乙醇酸、聚乳酸-乙醇酸、羟甲基纤维素、聚乙烯吡咯烷酮、硫酸软骨素、海藻糖、麦芽糖、半乳糖或蔗糖中的至少一种。
进一步的,所述模具使用聚四氟乙烯作为模具材料,模具凹槽为圆锥状,深度为100-500μm,圆锥底部直径为200-500μm。
采用以上制备方法,本发明具有如下优点:
微针属于中胚层疗法,微针作用于皮肤,刺入表皮内或表皮层下,形成无数微小通道,彻底破坏表皮牢固的屏障,使有效护肤成分经通道渗透,在皮下部位蓄积,足量直接作用,增强保湿、抗皱、抗氧化等护肤效果;玻尿酸具有高度的粘弹性、可塑性、渗透性以及独特的流变性能,是一种非常理想、安全可靠的生物材料和药物载体;本发明采用真空冷冻干燥机进行冻干,有效防止升温对微针内的活性成分的破坏;采用玻尿酸制备可溶性微针,可在皮肤内完全溶解,同时将内部包封的生物活性物质释放到人体皮肤内发挥作用,避免了金属微针对人体皮肤来的伤害和硅微针断裂的发生;添加多种天然活性提取物成分,减少了化学成分的使用,产品更加安全,赋予产品美白祛斑、延缓衰老、抗氧化、抗过敏、抗菌抗炎等功效。
具体实施方式
下面结合实施例对本发明做进一步的详细说明。
实施例一
一种玻尿酸微针贴片制备方法,包括以下原材料:微针溶液:透明质酸15%、活性提取物6%、神经酰胺3%、水解胶原蛋白4%、积雪草7%、聚赖氨酸1%和去离子水64%,基层原液:基质材料聚合物和去离子水,固液比为1:3,所述制备方法包括以下步骤:
(1)微针溶液的制备:称取去离子水64%,在低速搅拌的条件下,缓慢加入称量好的透明质酸15%,待透明质酸完全溶胀后,加入活性提取物6%、神经酰胺3%、水解胶原蛋白4%、积雪草7%、聚赖氨酸1%,加热并提高搅拌速度直至溶液沸腾,超声去除溶液中的气泡;
(2)基层原液的制备:称取基质材料按照固液比为1:3加入去离子水,搅拌至溶解,超声去除溶液中的气泡;
(3)模具的填充:取适量的微针溶液,倾倒于模具表面,均匀涂布后,使微针溶液进入并填满模具针状凹槽,将模具水平放置于真空干燥器内,打开真空泵,真空度为0.06MPa,连续抽真空1.5h,再加入基层原液,相同条件真空干燥;
(4)微针贴片的干燥:模具填充后,-80℃预冻1h,转入真空冷冻干燥机冻干24h;
(5)脱模:微针干燥至恒重后,缓慢剥离模具,即可得到微针贴片。
所述活性提取物为灵芝提取物和紫草根提取物。
所述基质材料聚合物为羟甲基纤维素。
所述模具使用聚四氟乙烯作为模具材料,模具凹槽为圆锥状,深度为100μm,圆锥底部直径为200μm。
实施例二
一种玻尿酸微针贴片制备方法,包括以下原材料:微针溶液:透明质酸13%、活性提取物5%、神经酰胺5%、水解胶原蛋白8%、积雪草8%、水杨酸1%和去离子水60%,基层原液:基质材料聚合物和去离子水,固液比为1:3,所述制备方法包括以下步骤:
(1)微针溶液的制备:称取去离子水60%,在低速搅拌的条件下,缓慢加入称量好的透明质酸13%,待透明质酸完全溶胀后,加入活性提取物5%、神经酰胺5%、水解胶原蛋白8%、积雪草8%、水杨酸1%,加热并提高搅拌速度直至溶液沸腾,超声去除溶液中的气泡;
(2)基层原液的制备:称取基质材料按照固液比为1:3加入去离子水,搅拌至溶解,超声去除溶液中的气泡;
(3)模具的填充:取适量的微针溶液,倾倒于模具表面,均匀涂布后,使微针溶液进入并填满模具针状凹槽,将模具水平放置于真空干燥器内,打开真空泵,真空度为0.09MPa,连续抽真空1h,再加入基层原液,相同条件真空干燥;
(4)微针贴片的干燥:模具填充后,-80℃预冻2h,转入真空冷冻干燥机冻干24h;
(5)脱模:微针干燥至恒重后,缓慢剥离模具,即可得到微针贴片。
所述活性提取物为银耳提取物、芦荟提取物、丹参提取物和紫草根提取物。
所述基质材料聚合物为硫酸软骨素。
所述模具使用聚四氟乙烯作为模具材料,模具凹槽为圆锥状,深度为500μm,圆锥底部直径为300μm。
实施例三
一种玻尿酸微针贴片制备方法,包括以下原材料:微针溶液:透明质酸14%、活性提取物6%、神经酰胺3%、水解胶原蛋白4%、积雪草6%、苯甲醇0.5%和去离子水66.5%,基层原液:基质材料聚合物和去离子水,固液比为1:3,所述制备方法包括以下步骤:
(1)微针溶液的制备:称取去离子水66.5%,在低速搅拌的条件下,缓慢加入称量好的透明质酸14%,待透明质酸完全溶胀后,加入活性提取物6%、神经酰胺3%、水解胶原蛋白4%、积雪草6%、苯甲醇0.5%,加热并提高搅拌速度直至溶液沸腾,超声去除溶液中的气泡;
(2)基层原液的制备:称取基质材料按照固液比为1:3加入去离子水,搅拌至溶解,超声去除溶液中的气泡;
(3)模具的填充:取适量的微针溶液,倾倒于模具表面,均匀涂布后,使微针溶液进入并填满模具针状凹槽,将模具水平放置于真空干燥器内,打开真空泵,真空度为0.08MPa,连续抽真空1.5h,再加入基层原液,相同条件真空干燥;
(4)微针贴片的干燥:模具填充后,-80℃预冻1h,转入真空冷冻干燥机冻干36h;
(5)脱模:微针干燥至恒重后,缓慢剥离模具,即可得到微针贴片。
所述活性提取物为芦荟提取物、红花提取物、红景天提取物和乳香提取物。
所述基质材料聚合物为聚乳酸和半乳糖。
所述模具使用聚四氟乙烯作为模具材料,模具凹槽为圆锥状,深度为300μm,圆锥底部直径为400μm。
以上所述,仅为本发明较佳的具体实施方式,但本发明的保护范围并不局限于此,任何熟悉本技术领域的技术人员在本发明揭露的技术范围内,根据本发明的技术方案及其发明构思加以等同替换或改变,都应涵盖在本发明的保护范围之内。
Claims (5)
1.一种玻尿酸微针贴片制备方法,其特征在于,包括以下原材料:微针溶液:透明质酸10-15%、活性提取物5-10%、神经酰胺3-6%、水解胶原蛋白4-8%、积雪草6-12%、防腐剂0.5-2%和去离子水60-72%,基层原液:基质材料聚合物和去离子水,固液比为1:3,所述制备方法包括以下步骤:
(1)微针溶液的制备:称取去离子水60-72%,在低速搅拌的条件下,缓慢加入称量好的透明质酸10-15%,待透明质酸完全溶胀后,加入活性提取物5-10%、神经酰胺3-6%、水解胶原蛋白4-8%、积雪草6-12%、防腐剂0.5-2%,加热并提高搅拌速度直至溶液沸腾,超声去除溶液中的气泡;
(2)基层原液的制备:称取基质材料按照固液比为1:3加入去离子水,搅拌至溶解,超声去除溶液中的气泡;
(3)模具的填充:取适量的微针溶液,倾倒于模具表面,均匀涂布后,使微针溶液进入并填满模具针状凹槽,将模具水平放置于真空干燥器内,打开真空泵,真空度为0.06-0.09MPa,连续抽真空1-1.5h,再加入基层原液,相同条件真空干燥;
(4)微针贴片的干燥:模具填充后,-80℃预冻1-2h,转入真空冷冻干燥机冻干24-36h;
(5)脱模:微针干燥至恒重后,缓慢剥离模具,即可得到微针贴片。
2.根据权利要求1所述的一种玻尿酸微针贴片制备方法,其特征在于,所述防腐剂包括聚赖氨酸、苯甲酸、水杨酸或苯甲醇中的至少一种。
3.根据权利要求1所述的一种玻尿酸微针贴片制备方法,其特征在于,所述活性提取物包括灵芝提取物、银耳提取物、芦荟提取物、红花提取物、丹参提取物、紫草根提取物、红景天提取物或乳香提取物中的至少一种。
4.根据权利要求1所述的一种玻尿酸微针贴片制备方法,其特征在于,所述基质材料聚合物包括聚乳酸、聚乙醇酸、聚乳酸-乙醇酸、羟甲基纤维素、聚乙烯吡咯烷酮、硫酸软骨素、海藻糖、麦芽糖、半乳糖或蔗糖中的至少一种。
5.根据权利要求1所述的一种玻尿酸微针贴片制备方法,其特征在于,所述模具使用聚四氟乙烯作为模具材料,模具凹槽为圆锥状,深度为100-500μm,圆锥底部直径为200-500μm。
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