CN109529015A - 一种女性hpv抗菌剂及其制备方法 - Google Patents
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Abstract
本发明公开了一种女性HPV抗菌剂及其制造方法,包括以下成分:丙二醇、芽孢杆菌发酵产物、氨基葡萄糖盐酸盐、谷胱甘肽、苦参、黄柏、蛇床子、当归、姜黄、鱼腥草、益母草、山药、紫草、苯氧乙醇、水溶凉感剂HK8465和卡波U20,所述丙二醇占比为4%、所述芽孢杆菌发酵产物占比为1%、所述氨基葡萄糖盐酸盐占比为8.97%、所述谷胱甘肽占比为5%、所述苦参占比为15%、所述黄柏占比为10%、所述蛇床子占比为5%、所述当归占比为5%、所述姜黄占比为5%、所述鱼腥草占比为10%、所述益母草占比为15%、所述山药占比为5%、所述紫草占比为10%、所述苯氧乙醇占比为0.5%、所述水溶凉感剂HK8465占比为0.03%和所述卡波占U20比为0.5%。
Description
技术领域
本发明涉及医药技术领域,尤其是涉及一种女性HPV抗菌剂及其制备方法。
背景技术
人类乳头瘤病毒(Human Papilloma Virus,简称HPV)是一种嗜上皮性病毒,有高度的特异性,长期以来,已知HPV可引起人类良性的肿瘤和疣,如生长在生殖器官附近皮肤和粘膜上的人类寻常疣、尖锐湿疣以及生长在粘膜上的乳头状瘤。像乙肝病毒一样,HPV也是一种DNA病毒。它原是多瘤空泡病毒科的一员,1999年国际病毒分类委员会(ICTV)取消多瘤空泡病毒科,代之以乳头瘤病毒科,因此,HPV便归属此门下。HPV感染途径⒈性传播途径;⒉密切接触;⒊间接接触:通过接触感染者的衣物、生活用品、用具等;⒋医源性感染:医务人员在治疗护理时防护不好,造成自身感染或通过医务人员传给患者;⒌母婴传播:是由婴儿通过孕妇产道的密切接触;
75%的女人会在一生中感染过HPV病毒(人乳头瘤状病毒,99%的宫颈癌与其相关),但又有90%的女人会在1-2年内依靠自身免疫系统将HPV病毒清除出体外,只有极少数的“漏网之鱼”会发展为宫颈癌。目前,已知的HPV有100多种不同类型,其中大部分类型被视为“低风险”,与宫颈癌并无关联。但有14种HPV类型被列为“高风险”,并已经证实它们会导致几乎所有的宫颈癌;
目前针对HPV的治疗主要是通过手术、针剂注射和口服药物治疗,这些方法由于是西药,对于身体伤害副作用大,还有通过外用药物治疗,例如通过在病患处给药,常用的药物有栓剂,泡腾片等,但这些药物或多或少存在缺陷,作用较为单一。
发明内容
本发明要解决的技术问题是克服现有的缺陷,提供一种女性HPV抗菌剂及其制备方法,从而解决上述问题。
为实现上述目的,本发明提供如下技术方案一种女性HPV抗菌剂,包括以下成分:丙二醇、芽孢杆菌发酵产物、氨基葡萄糖盐酸盐、谷胱甘肽、苦参、黄柏、蛇床子、当归、姜黄、鱼腥草、益母草、山药、紫草、苯氧乙醇、水溶凉感剂HK8465和卡波U20,所述丙二醇占比为4%、所述芽孢杆菌发酵产物占比为1%、所述氨基葡萄糖盐酸盐占比为8.97%、所述谷胱甘肽占比为5%、所述苦参占比为15%、所述黄柏占比为10%、所述蛇床子占比为5%、所述当归占比为5%、所述姜黄占比为5%、所述鱼腥草占比为10%、所述益母草占比为15%、所述山药占比为5%、所述紫草占比为10%、所述苯氧乙醇占比为0.5%、所述水溶凉感剂HK8465占比为0.03%和所述卡波占U20比为0.5%。
本发明还提供一种女性HPV抗菌剂的制备方法,其特征在于,包括以下步骤;
步骤一;准备材料:按照比例准备:所述丙二醇占比为4%、所述芽孢杆菌发酵产物占比为1%、所述氨基葡萄糖盐酸盐占比为8.97%、所述谷胱甘肽占比为5%、所述苦参占比为15%、所述黄柏占比为10%、所述蛇床子占比为5%、所述当归占比为5%、所述姜黄占比为5%、所述鱼腥草占比为10%、所述益母草占比为15%、所述山药占比为5%、所述紫草占比为10%、所述苯氧乙醇占比为0.5%、所述水溶凉感剂HK8465占比为0.03%和所述卡波占U20比为0.5%;
步骤二:先添加按比例准备好的所述丙二醇、所述芽孢杆菌发酵产物,要先增容透明,增容透明了才加入去离子水;
步骤三;然后向步骤二中溶液内逐一添加氨基葡萄糖盐酸盐、谷胱甘肽、苦参、黄柏、蛇床子、当归、姜黄、鱼腥草、益母草、山药、紫草、苯氧乙醇、水溶凉感剂HK8465;
步骤四;最后在步骤三的溶液内添加卡波占U20,刚投入下去30分钟内不要搅拌,卡波散开溶解来再进行搅拌。
作为本发明一种女性HPV抗菌剂的制备方法的一种优选技术方案,溶液的PH值控制在6.5-7之间。
与现有技术相比,本发明的有益效果是:本发明立足于对HPV发病机理和治疗原理,配伍合理、科学,经大量临床验证,无毒无副作用,本发明的产品涂于患处以后,能迅速扩散至不适处,深入肌理,通过药物组合发挥的药效促进细胞新陈代谢,从而增强细胞对药物的吸收能力,在皮肤表面形成一层薄膜,有效阻绝外来细菌的侵入,并快速修复皮肤组织,提高创口愈合再生能力,该凝胶中的多种植物提取物还能够提高机体免疫力,能起到良好的抗病毒效果。
具体实施方式
对本发明实施例中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做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。
本发明提供一种技术方案:一种女性HPV抗菌剂,包括以下成分:丙二醇、芽孢杆菌发酵产物、氨基葡萄糖盐酸盐、谷胱甘肽、苦参、黄柏、蛇床子、当归、姜黄、鱼腥草、益母草、山药、紫草、苯氧乙醇、水溶凉感剂HK8465和卡波U20,所述丙二醇占比为4%、所述芽孢杆菌发酵产物占比为1%、所述氨基葡萄糖盐酸盐占比为8.97%、所述谷胱甘肽占比为5%、所述苦参占比为15%、所述黄柏占比为10%、所述蛇床子占比为5%、所述当归占比为5%、所述姜黄占比为5%、所述鱼腥草占比为10%、所述益母草占比为15%、所述山药占比为5%、所述紫草占比为10%、所述苯氧乙醇占比为0.5%、所述水溶凉感剂HK8465占比为0.03%和所述卡波占U20比为0.5%。
本发明还提供一种女性HPV抗菌剂的制备方法,其特征在于,包括以下步骤;
步骤一;准备材料:按照比例准备:所述丙二醇占比为4%、所述芽孢杆菌发酵产物占比为1%、所述氨基葡萄糖盐酸盐占比为8.97%、所述谷胱甘肽占比为5%、所述苦参占比为15%、所述黄柏占比为10%、所述蛇床子占比为5%、所述当归占比为5%、所述姜黄占比为5%、所述鱼腥草占比为10%、所述益母草占比为15%、所述山药占比为5%、所述紫草占比为10%、所述苯氧乙醇占比为0.5%、所述水溶凉感剂HK8465占比为0.03%和所述卡波占U20比为0.5%;
步骤二:先添加按比例准备好的所述丙二醇、所述芽孢杆菌发酵产物,要先增容透明,增容透明了才加入去离子水;
步骤三;然后向步骤二中溶液内逐一添加氨基葡萄糖盐酸盐、谷胱甘肽、苦参、黄柏、蛇床子、当归、姜黄、鱼腥草、益母草、山药、紫草、苯氧乙醇、水溶凉感剂HK8465;
步骤四;最后在步骤三的溶液内添加卡波占U20,刚投入下去30分钟内不要搅拌,卡波散开溶解来再进行搅拌。
作为本发明一种女性HPV抗菌剂的制备方法的一种优选技术方案,溶液的PH值控制在6.5-7之间。
本发明立足于对HPV发病机理和治疗原理,配伍合理、科学,经大量临床验证,无毒无副作用,本发明的产品涂于患处以后,能迅速扩散至不适处,深入肌理,通过药物组合发挥的药效促进细胞新陈代谢,从而增强细胞对药物的吸收能力,在皮肤表面形成一层薄膜,有效阻绝外来细菌的侵入,并快速修复皮肤组织,提高创口愈合再生能力,该凝胶中的多种植物提取物还能够提高机体免疫力,能起到良好的抗病毒效果。
最后应说明的是:以上所述仅为本发明的优选实施例而已,并不用于限制本发明,尽管参照前述实施例对本发明进行了详细的说明,对于本领域的技术人员来说,其依然可以对前述各实施例所记载的技术方案进行修改,或者对其中部分技术特征进行等同替换,凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
Claims (3)
1.一种女性HPV抗菌剂及其制造方法,其特征在于,包括以下成分:丙二醇、芽孢杆菌发酵产物、氨基葡萄糖盐酸盐、谷胱甘肽、苦参、黄柏、蛇床子、当归、姜黄、鱼腥草、益母草、山药、紫草、苯氧乙醇、水溶凉感剂HK8465和卡波U20,所述丙二醇占比为4%、所述芽孢杆菌发酵产物占比为1%、所述氨基葡萄糖盐酸盐占比为8.97%、所述谷胱甘肽占比为5%、所述苦参占比为15%、所述黄柏占比为10%、所述蛇床子占比为5%、所述当归占比为5%、所述姜黄占比为5%、所述鱼腥草占比为10%、所述益母草占比为15%、所述山药占比为5%、所述紫草占比为10%、所述苯氧乙醇占比为0.5%、所述水溶凉感剂HK8465占比为0.03%和所述卡波占U20比为0.5%。
2.一种女性HPV抗菌剂的制备方法,其特征在于,包括以下步骤;
步骤一;准备材料:按照比例准备:所述丙二醇占比为4%、所述芽孢杆菌发酵产物占比为1%、所述氨基葡萄糖盐酸盐占比为8.97%、所述谷胱甘肽占比为5%、所述苦参占比为15%、所述黄柏占比为10%、所述蛇床子占比为5%、所述当归占比为5%、所述姜黄占比为5%、所述鱼腥草占比为10%、所述益母草占比为15%、所述山药占比为5%、所述紫草占比为10%、所述苯氧乙醇占比为0.5%、所述水溶凉感剂HK8465占比为0.03%和所述卡波占U20比为0.5%;
步骤二:先添加按比例准备好的所述丙二醇、所述芽孢杆菌发酵产物,要先增容透明,增容透明了才加入去离子水;
步骤三;然后向步骤二中溶液内逐一添加氨基葡萄糖盐酸盐、谷胱甘肽、苦参、黄柏、蛇床子、当归、姜黄、鱼腥草、益母草、山药、紫草、苯氧乙醇、水溶凉感剂HK8465;
步骤四;最后在步骤三的溶液内添加卡波占U20,刚投入下去30分钟内不要搅拌,卡波散开溶解来再进行搅拌。
3.根据权利要求2所述的一种女性HPV抗菌剂的制备方法,其特征在于,溶液的PH值控制在6.5-7之间。
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