CN109999175A - 一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂及其制备方法 - Google Patents
一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂及其制备方法 Download PDFInfo
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- CN109999175A CN109999175A CN201910283674.XA CN201910283674A CN109999175A CN 109999175 A CN109999175 A CN 109999175A CN 201910283674 A CN201910283674 A CN 201910283674A CN 109999175 A CN109999175 A CN 109999175A
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Abstract
本发明公开了一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂及其制备方法,由以下重量份的原料组成:水杨酸:0.001‑0.005mg;左旋Vc:2‑15g;鱼腥草提取物:2‑10g;金银花提取物:3‑16g;柠檬酸:10‑30g;维生素A:10‑30g;茅岩莓提取物:2‑26g;马齿笕提取物:2‑30g;纳米银溶液:0.002‑0.009mg;没药:5‑35g;寡肽‑1:0.02‑0.09mg;积雪草提取物:0.03‑0.09g;蒸馏水:750‑1000g。本发明的复合制剂通过纳米银、水杨酸、茅岩莓、马齿笕鳌合多种消炎杀菌成分,消除暗疮脓肿、皮炎感染、粉刺溃疡,有机复合多种有效成分配方,将其功效提高到鳌合前的数倍,对皮炎感染、粉刺暗疮、口腔溃疡、鼻炎均具良好的改善消除作用,同时该复合制剂原料获取容易,制备简单,具有操作简单、便于应用、疗效显著的优点。
Description
技术领域
本发明涉及水液制剂技术领域,特别是涉及一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂及其制备方法。
背景技术
目前,由于环境污染,饮食不当,精神压力等因素造成人体过氧化,体内自由基大量堆积,内在表现为体内氧化中毒,氧化燃烧形成炎症感染,溃疡脓肿,其机理为:红肿炎症感染溃疡发生时,由于中性粒细胞和巨噬细胞释放大量的自由基(·OH、·O2等),被称为“呼吸爆发”或“氧化燃烧”,结果是自由基破坏正常的组织细胞结构引起局部红肿炎症感染发生,如粉刺暗疮发生过程中,“氧化燃烧”自由基对正常皮肤细胞细胞的破坏作用引起***细胞变异、粉刺杆菌感染发炎。外在表现多为;暗疮脓肿、皮炎感染、粉刺溃疡。例如;粉刺暗疮、口腔溃疡、鼻炎等症状普遍存在。
目前市面上并没有消除暗疮脓肿皮炎感染粉刺溃疡的专用药剂,很多都是通过黄瓜汁、白醋等混合后洗脸和搓脸来进行治疗的,再有就是通过输液或者长期服用具有消炎作用的西药来治疗暗疮、痘痘。这些方法都效果差,不能完全根治。
发明内容
本发明的目的就在于为了解决上述问题而提供一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,利用纳米银、水杨酸、鱼腥草、茅岩莓、柠檬酸等植物提取物强有力消除炎症感染,灭菌消肿功能再加上其它植物成分复合配方来达到治疗暗疮脓肿、皮炎感染、粉刺溃疡的目的。
本发明通过以下技术方案来实现上述目的:
一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,由以下重量份的原料组成:水杨酸:0.001-0.005mg;左旋Vc:2-15g;鱼腥草提取物:2-10g;金银花提取物:3-16g;柠檬酸:10-30g;维生素A:10-30g;茅岩莓提取物:2-26g;马齿笕提取物:2-30g;纳米银溶液:0.002-0.009mg;没药:5-35g;寡肽-1:0.02-0.09mg;积雪草提取物:0.03-0.09g;蒸馏水:750-1000g。
进一步的,它主要由如下最佳重量份配比的原材料组成:水杨酸:0.002mg;左旋Vc:8g;鱼腥草提取物:6g;金银花提取物:9g;柠檬酸:10g;维生素A:20g;茅岩莓提取物:3g;马齿笕提取物:10g;纳米银溶液:0.006mg;没药:10g;寡肽-1:0.06mg;积雪草提取物:0.03g;蒸馏水:800g。
进一步的,没药使用前经过研磨处理,得到粉末状药粉。
本发明还提供一种用于制备上述用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂的制备方法,包括如下步骤:
(1)按上述配方重量计,取水杨酸、鱼腥草提取物、马齿笕提取物、茅岩莓、柠檬酸及蒸馏水混合,并加热至85℃,保温搅拌15分钟、以15转/分钟的转速搅拌,得A相溶液;
(2)按上述配方重量计,取金银花提取物、纳米银溶液、寡肽-1、积雪草提取物、没药、维生素A、左旋Vc混合,均质7分钟后,加热至55℃得B相溶液;
(3)得到上述B相溶液后保温并以45转/分钟的搅拌速度搅拌,在搅拌下将上述A相溶液滴入到上述B相溶液中,搅拌均匀后过滤和冷却,冷却完全后制成水液剂;
(4)在无菌条件下将上述水液剂进行灌装和包装储存。
进一步的,所述步骤(3)中搅拌时间为30-45min。
本发明中的药材纯度要求:
水杨酸有效成分纯度99%,左旋Vc有效纯度99%,鱼腥草提取物有效成分纯度98%,金银花提取物有效成分纯度90%,柠檬酸有效成分纯度98%,维生素A有效成分纯度98%,茅岩莓提取物有效纯度98%,马齿笕提取物有效成分纯度90%,纳米银溶液有效成分纯度98%,没药有效成分纯度98%,寡肽-1有效成分纯度99%;积雪草提取物有效成分纯度90%。
本发明的药材功效解析如下:
鱼腥草:味辛,微寒;归肺经;功能与主治:清热解毒,消痈排脓,利尿通淋;用于肺痈吐脓,痰热喘咳,热痢,热淋,痈肿疮毒;
金银花:味甘、性寒;归肺、心、胃经,功用主治:清热,解毒;治温病发热,热毒血痢,痈疡,肿毒,瘰疬,痔漏;
马齿笕:性寒,味甘酸;入心、肝、脾、大肠经;功效主治:清热解毒,利水去湿,散血消肿,除尘杀菌,消炎止痛,止血凉血;主治痢疾,肠炎,肾炎,产后子宫出血,便血,乳腺炎等病症;
没药:味苦辛,性平,无毒,入十二经,功用主治:散血去瘀,消肿定痛;治跌损,金疮,筋骨,心腹诸痛,癥瘕,闭经,痈疽肿痛,痔漏,目障;
积雪草:味苦、辛,性寒;归肝、脾、肾经;功能与主治:清热利湿,解毒消肿:用于湿热黄疸,中暑腹泻,砂淋血淋,痈肿疮毒,跌扑损伤;
本发明中其他原料功效解析如下:
纳米银:纳米银外用一种广谱抗菌物质,能够缓释放出纳米银抑制并杀灭与之接触的病菌,包括痤疮丙酸杆菌、糠秕孢子菌、表皮葡萄球菌,并有促进皮肤愈合的作用;
水杨酸:水杨酸抗茵诈用强、抗菌谱广,水杨酸对常见细菌具有显著的抗菌作用,水扬酸对格兰氏阳性菌、格曼氏阴性菌耐黄色葡萄球菌均有灭活作用;
茅岩莓:茅岩莓具有很强的抗菌消炎作用减少炎性细胞的参与、活化血液中红细胞,增加血红蛋白的含量,提高氧的利用率,减轻各种慢性炎症,茅岩莓通过对杆菌有灭活作用,消除口腔粘膜的炎症,促进鼻炎粘膜溃疡愈合;
寡肽-1:防粉刺、祛疤痕,由于EGF能刺激肉芽组织的形成和促进肉芽组织的上皮化,还可调节胶原降解及更新,使胶原纤维以线性方式排列,防止***异常增生,故而有缩短创伤愈合时间以及减少疤痕形成的作用,对防止痤疮的形成有很好的效果;
左旋Vc:促进骨胶原的生物合成,利于组织创伤口的更快愈合,促进牙齿和骨骼的生长,防止牙床出血,防止关节痛、腰腿痛;增强肌体对外界环境的抗应激能力和免疫力;维生素C,可使皮肤黑色素沉着减少,从而减少黑斑和雀斑,使皮肤白皙;
维生素A:有抗呼吸***感染作用;有助于免疫***功能正常;能保持组织或器官表层的健康;有助于祛除老年斑;外用有助于对粉刺、脓包、疖疮,皮肤表面溃疡等症的治疗;
本发明的有益效果在于:本发明的复合制剂通过纳米银、水杨酸、茅岩莓、马齿笕鳌合多种消炎杀菌成分,消除暗疮脓肿、皮炎感染、粉刺溃疡,有机复合多种有效成分配方,将其功效提高到鳌合前的数倍,对皮炎感染、粉刺暗疮、口腔溃疡、鼻炎均具良好的改善消除作用,同时该复合制剂原料获取容易,制备简单,具有操作简单、便于应用、疗效显著的优点。
具体实施方式
下面将结合实施例对本发明的技术方案进行清楚、完整地描述,显然,所描述的实施例仅仅是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有作出创造性劳动前提下所获得的所有其他实施例,都属于本发明保护的范围。
实施例一:
一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,由以下重量份的原料组成:水杨酸:0.002mg;左旋Vc:8g;鱼腥草提取物:6g;金银花提取物:9g;柠檬酸:10g;维生素A:20g;茅岩莓提取物:3g;马齿笕提取物:10g;纳米银溶液:0.006mg;没药:10g;寡肽-1:0.06mg;积雪草提取物:0.03g;蒸馏水:800g。
实施例二:
一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,由以下重量份的原料组成:水杨酸:0.001mg;左旋Vc:2g;鱼腥草提取物:10g;金银花提取物:5g;柠檬酸:15g;维生素A:15g;茅岩莓提取物:8g;马齿笕提取物:29g;纳米银溶液:0.005mg;没药:18g;寡肽-1:0.02mg;积雪草提取物:0.08g;蒸馏水:750g。
实施例三:
一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,由以下重量份的原料组成:水杨酸:0.003mg;左旋Vc:15g;鱼腥草提取物:15g;金银花提取物:15g;柠檬酸:25g;维生素A:28g;茅岩莓提取物:9g;马齿笕提取物:15g;纳米银溶液:0.006mg;没药:22g;寡肽-1:0.09mg;积雪草提取物:0.07g;蒸馏水:800g。
实施例四:
一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,由以下重量份的原料组成:水杨酸:0.002mg;左旋Vc:4g;鱼腥草提取物:5g;金银花提取物:12g;柠檬酸:26g;维生素A:19g;茅岩莓提取物:6g;马齿笕提取物:20g;纳米银溶液:0.002mg;没药:16g;寡肽-1:0.07mg;积雪草提取物:0.09g;蒸馏水:870g。
实施例五:
一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,由以下重量份的原料组成:水杨酸:0.004mg;左旋Vc:10g;鱼腥草提取物:25g;金银花提取物:8g;柠檬酸:18g;维生素A:25g;茅岩莓提取物:10g;马齿笕提取物:18g;纳米银溶液:0.003mg;没药:12g;寡肽-1:0.03mg;积雪草提取物:0.06g;蒸馏水:895g。
实施例六:
一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,由以下重量份的原料组成:水杨酸:0.005mg;左旋Vc:11g;鱼腥草提取物:20g;金银花提取物:8g;柠檬酸:30g;维生素A:30g;茅岩莓提取物:7g;马齿笕提取物:25;纳米银溶液:0.009mg;没药:25g;寡肽-1:0.08mg;积雪草提取物:0.04g;蒸馏水:950g。
实施例七:
一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,由以下重量份的原料组成:水杨酸:0.001mg;左旋Vc:10g;鱼腥草提取物:8g;金银花提取物:10g;柠檬酸:28g;维生素A:10g;茅岩莓提取物:15g;马齿笕提取物:8g;纳米银溶液:0.007mg;没药:15g;寡肽-1:0.05mg;积雪草提取物:0.05g;蒸馏水:900g。
实施例八:
一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,由以下重量份的原料组成:水杨酸:0.003mg;左旋Vc:9g;鱼腥草提取物:26g;金银花提取物:13g;柠檬酸:22g;维生素A:20g;茅岩莓提取物:16g;马齿笕提取物:13g;纳米银溶液:0.005mg;没药:30g;寡肽-1:0.04mg;积雪草提取物:0.06g;蒸馏水:850g。
本发明还提供一种用于制备上述用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂的制备方法,包括如下步骤:
(1)按上述配方重量计,取水杨酸、鱼腥草提取物、马齿笕提取物、茅岩莓、柠檬酸及蒸馏水混合,并加热至85℃,保温搅拌15分钟、以15转/分钟的转速搅拌,得A相溶液;
(2)按上述配方重量计,取金银花提取物、纳米银溶液、寡肽-1、积雪草提取物、没药、维生素A、左旋Vc混合,均质7分钟后,加热至55℃得B相溶液;
(3)得到上述B相溶液后保温并以45转/分钟的搅拌速度搅拌,在搅拌下将上述A相溶液滴入到上述B相溶液中,搅拌均匀后过滤和冷却,冷却完全后制成水液剂;
(4)在无菌条件下将上述水液剂进行灌装和包装储存。
进一步的,所述步骤(3)中搅拌时间为30-45min。
本发明中的药材纯度要求:
水杨酸有效成分纯度99%,左旋Vc有效纯度99%,鱼腥草提取物有效成分纯度98%,金银花提取物有效成分纯度90%,柠檬酸有效成分纯度98%,维生素A有效成分纯度98%,茅岩莓提取物有效纯度98%,马齿笕提取物有效成分纯度90%,纳米银溶液有效成分纯度98%,没药有效成分纯度98%,寡肽-1有效成分纯度99%;积雪草提取物有效成分纯度90%。
以下为使用本发明复合制剂的临床例子:
1:刘某某,男,19岁,脸部有中度粉刺暗疮,使用本制剂一星期后有明显效果,两星期后脸上粉刺全部消失。
2:王某某,女,38岁,有中度鼻炎脓肿,使用本制剂两星期后,鼻出血现象消失,一个月后,脓肿消失,鼻腔通透。
3:杨某,男,53岁,口腔溃疡一个星期没见好,使用本制剂后1天疼痛感觉消失,3天后痊愈。
选取粉刺暗疮、口腔溃疡、鼻炎皮疹患者各三十名进行临床实验,实验效果如下:
种类 | 病例人数 | 观察时间 | 有效治疗 | 完全治愈 | 无效 |
粉刺暗疮 | 30 | 15天 | 3 | 27 | 0 |
口腔溃疡 | 30 | 4天 | 2 | 28 | 0 |
鼻炎皮疹 | 30 | 30天 | 5 | 24 | 1 |
经初步统计,在对消除暗疮粉刺、口腔溃疡、鼻炎皮疹效果良好,有效率达到90%以上;同时使用本发明对皮肤止痒消炎伤口感染等也有很好的愈合作用,有效率达到80%以上。
以上显示和描述了本发明的基本原理、主要特征和优点。本行业的技术人员应该了解,本发明不受上述实施例的限制,上述实施例和说明书中描述的只是说明本发明的原理,在不脱离本发明精神和范围的前提下,本发明还会有各种变化和改进,这些变化和改进都落入要求保护的本发明范围内。
Claims (5)
1.一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,其特征在于:由以下重量份的原料组成:水杨酸:0.001-0.005mg;左旋Vc:2-15g;鱼腥草提取物:2-10g;金银花提取物:3-16g;柠檬酸:10-30g;维生素A:10-30g;茅岩莓提取物:2-26g;马齿笕提取物:2-30g;纳米银溶液:0.002-0.009mg;没药:5-35g;寡肽-1:0.02-0.09mg;积雪草提取物:0.03-0.09g;蒸馏水:750-1000g。
2.根据权利要求1所述的一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,其特征在于:它主要由如下最佳重量份配比的原材料组成:水杨酸:0.002mg;左旋Vc:8g;鱼腥草提取物:6g;金银花提取物:9g;柠檬酸:10g;维生素A:20g;茅岩莓提取物:3g;马齿笕提取物:10g;纳米银溶液:0.006mg;没药:10g;寡肽-1:0.06mg;积雪草提取物:0.03g;蒸馏水:800g。
3.根据权利要求1所述的一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂,其特征在于:没药使用前经过研磨处理,得到粉末状药粉。
4.制备权利要求1或2所述的用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂的制备方法,其特征在于:包括如下步骤:
按上述配方重量计,取水杨酸、鱼腥草提取物、马齿笕提取物、茅岩莓、柠檬酸及蒸馏水混合,并加热至85℃,保温搅拌15分钟、以15转/分钟的转速搅拌,得A相溶液;
按上述配方重量计,取金银花提取物、纳米银溶液、寡肽-1、积雪草提取物、没药、维生素A、左旋Vc混合,均质7分钟后,加热至55℃得B相溶液;
得到上述B相溶液后保温并以45转/分钟的搅拌速度搅拌,在搅拌下将上述A相溶液滴入到上述B相溶液中,搅拌均匀后过滤和冷却,冷却完全后制成水液剂;
在无菌条件下将上述水液剂进行灌装和包装储存。
5.根据权利要求4所述的一种用于消除暗疮脓肿皮炎感染粉刺溃疡的复合制剂的制备方法,其特征在于:所述步骤(3)中搅拌时间为30-45min。
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