CN106344764A - 一种中药口腔护理液及其制备方法 - Google Patents

一种中药口腔护理液及其制备方法 Download PDF

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CN106344764A
CN106344764A CN201610782304.7A CN201610782304A CN106344764A CN 106344764 A CN106344764 A CN 106344764A CN 201610782304 A CN201610782304 A CN 201610782304A CN 106344764 A CN106344764 A CN 106344764A
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宋继武
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Abstract

本发明公开了一种中药口腔护理液及其制备方法，由藏红花、田旋花、金银花、芦荟、氯化钠、灯心、玄参、决明子、艾叶、鱼腥草、桔梗、维生素C、薄荷脑和蒸馏水制备而成，将上述草药分别研磨，按配比混合，放入密闭的容器中，通入水蒸气处理，立即放入乙醇中进行超声处理，过滤去渣向滤液中加入维生素C、薄荷脑和蒸馏水，搅拌均匀，密封装罐即可。本发明的口腔护理液，制作方法简单，不含化学抑菌剂，无毒副作用，口感天然纯正，既适合口腔不适时使用，也适宜日常口腔护理，可有效清洁口腔和牙齿，缓解牙痛、牙龈出血、口腔溃疡、牙周炎、咽喉肿痛等不适症状，保护口腔的健康。

Description

一种中药口腔护理液及其制备方法
技术领域
本发明涉及中药技术领域，具体是一种中药口腔护理液及其制备方法。
背景技术
口腔、咽喉是进食和呼吸的通道，又是饮食水进入人体的必经之路，与人的健康生存息息相关。所以，其健康对人体产生重要的影响，细菌及病毒感染，空气污染，用声过度、烟酒及辛辣燥热刺激食物等因素易导致口腔问题、咽喉炎症，如果失治、误治、错治，易演变成牙周炎、慢性咽喉炎等。对慢性咽喉炎的治疗，虽然很多药物，但临床实践证实，不仅疗效不十分满意，且副作用大。
目前在临床上应用的口腔消毒剂主要由碘类、抗生素类、酸碱类或洗必泰类。碘离子氧化能力极强，但不稳定，又易于其它物质产生颜色变化，同时产生沉淀，消毒杀菌作用也随之降低；抗生素类如呋喃西林，口感差且容易产生抑菌性；酸碱类或洗必泰类其成本高、杀菌效率低、稳定性差，有毒性、腐蚀性或刺激性气味，对口腔粘膜有一定的损伤，口腔臭味无法消除，消毒后还需要大量的清水冲洗，如果误吞将造成一定的损伤。
因此，为克服上述口腔护理液存在的诸多不足，我们根据多种中草药不同药理作用，制成了一种中药口腔护理液，在预防和治疗口腔溃疡中发挥了重要作用。
发明内容
本发明的目的在于提供一种中药口腔护理液及其制备方法，以解决上述背景技术中提出的问题。
为实现上述目的，本发明提供如下技术方案：
一种中药口腔护理液，由以下重量份的原料制备而成：藏红花16～20份，田旋花12～16份，金银花18～24份，芦荟10～14份，氯化钠6～8份，灯心4～6份，玄参7～9份，决明子4～6份，艾叶11～13份，鱼腥草5～7份，桔梗11～15份，维生素C 0.5～0.9份，薄荷脑0.1～0.2份，蒸馏水150～200份。
作为本发明进一步的方案：具体由以下重量份的原料制备而成：藏红花18份，田旋花14份，金银花21份，芦荟12份，氯化钠7份，灯心5份，玄参8份，决明子5份，艾叶12份，鱼腥草6份，桔梗13份，维生素C 0.7份，薄荷脑0.15份，水180份。
一种所述的中药口腔护理液的制备方法，步骤如下：将藏红花、田旋花、金银花、芦荟、氯化钠、灯心、玄参、决明子、艾叶、鱼腥草、桔梗分别研磨至80～100目，按配比称取混合得到中药粉；将中药粉放入密闭的容器中，通入温度为290～300℃，压力为8～10MPa的水蒸气，处理6～8min，将处理后的中药粉混合液立即放入体积分数为80～85％的乙醇中，中药粉混合液与乙醇的体积比为1:6～8，在超声温度为58～62℃下用300～350r/min的搅拌速率搅拌20～24min，在超声温度为98～102℃下用300～350r/min的搅拌速率搅拌3～5min，过滤去渣，得到滤液，向滤液中加入维生素C、薄荷脑和蒸馏水，搅拌均匀，密封装罐即可。
与现有技术相比，本发明的有益效果是：
本发明的口腔护理液，制作方法简单，不含化学抑菌剂，无毒副作用，口感天然纯正，既适合口腔不适时使用，也适宜日常口腔护理，可有效清洁口腔和牙齿，缓解牙痛、牙龈出血、口腔溃疡、牙周炎、咽喉肿痛等不适症状，保护口腔的健康。
具体实施方式
下面将结合本发明实施例，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。
实施例1
中药口腔护理液，由以下重量份的原料制备而成：藏红花16份，田旋花16份，金银花18份，芦荟14份，氯化钠6份，灯心6份，玄参7份，决明子6份，艾叶11份，鱼腥草7份，桔梗11份，维生素C 0.9份，薄荷脑0.1份，蒸馏水150份。
上述中药口腔护理液的制备步骤如下：将藏红花、田旋花、金银花、芦荟、氯化钠、灯心、玄参、决明子、艾叶、鱼腥草、桔梗分别研磨至80目，按配比称取混合得到中药粉；将中药粉放入密闭的容器中，通入温度为290℃，压力为10MPa的水蒸气，处理6min，将处理后的中药粉混合液立即放入体积分数为80％的乙醇中，中药粉混合液与乙醇的体积比为1:6，在超声温度为58～62℃下用300～350r/min的搅拌速率搅拌20～24min，在超声温度为98～102℃下用300～350r/min的搅拌速率搅拌3～5min，过滤去渣，得到滤液，向滤液中加入维生素C、薄荷脑和蒸馏水，搅拌均匀，密封装罐即可。
实施例2
中药口腔护理液，由以下重量份的原料制备而成：藏红花18份，田旋花14份，金银花21份，芦荟12份，氯化钠7份，灯心5份，玄参8份，决明子5份，艾叶12份，鱼腥草6份，桔梗13份，维生素C 0.7份，薄荷脑0.15份，水180份。
上述中药口腔护理液的制备步骤如下：将藏红花、田旋花、金银花、芦荟、氯化钠、灯心、玄参、决明子、艾叶、鱼腥草、桔梗分别研磨至90目，按配比称取混合得到中药粉；将中药粉放入密闭的容器中，通入温度为295℃，压力为9MPa的水蒸气，处理7min，将处理后的中药粉混合液立即放入体积分数为83％的乙醇中，中药粉混合液与乙醇的体积比为1:7，在超声温度为60℃下用325r/min的搅拌速率搅拌22min，在超声温度为100℃下用325r/min的搅拌速率搅拌4min，过滤去渣，得到滤液，向滤液中加入维生素C、薄荷脑和蒸馏水，搅拌均匀，密封装罐即可。
实施例3
中药口腔护理液，由以下重量份的原料制备而成：藏红花20份，田旋花12份，金银花24份，芦荟10份，氯化钠8份，灯心4份，玄参9份，决明子4份，艾叶13份，鱼腥草5份，桔梗15份，维生素C 0.5份，薄荷脑0.2份，蒸馏水200份。
上述中药口腔护理液的制备步骤如下：将藏红花、田旋花、金银花、芦荟、氯化钠、灯心、玄参、决明子、艾叶、鱼腥草、桔梗分别研磨至100目，按配比称取混合得到中药粉；将中药粉放入密闭的容器中，通入温度为300℃，压力为8MPa的水蒸气，处理8min，将处理后的中药粉混合液立即放入体积分数为85％的乙醇中，中药粉混合液与乙醇的体积比为1:8，在超声温度为62℃下用350r/min的搅拌速率搅拌24min，在超声温度为102℃下用350r/min的搅拌速率搅拌5min，过滤去渣，得到滤液，向滤液中加入维生素C、薄荷脑和蒸馏水，搅拌均匀，密封装罐即可。
对于本领域技术人员而言，显然本发明不限于上述示范性实施例的细节，而且在不背离本发明的精神或基本特征的情况下，能够以其他的具体形式实现本发明。因此，无论从哪一点来看，均应将实施例看作是示范性的，而且是非限制性的，本发明的范围由所附权利要求而不是上述说明限定，因此旨在将落在权利要求的等同要件的含义和范围内的所有变化囊括在本发明内。

Claims (3)

1.一种中药口腔护理液，其特征在于，由以下重量份的原料制备而成：藏红花16～20份，田旋花12～16份，金银花18～24份，芦荟10～14份，氯化钠6～8份，灯心4～6份，玄参7～9份，决明子4～6份，艾叶11～13份，鱼腥草5～7份，桔梗11～15份，维生素C 0.5～0.9份，薄荷脑0.1～0.2份，蒸馏水150～200份。
2.根据权利要求1所述的中药口腔护理液及其制备方法，其特征在于，具体由以下重量份的原料制备而成：藏红花18份，田旋花14份，金银花21份，芦荟12份，氯化钠7份，灯心5份，玄参8份，决明子5份，艾叶12份，鱼腥草6份，桔梗13份，维生素C 0.7份，薄荷脑0.15份，水180份。
3.一种如权利要求1或2所述的中药口腔护理液的制备方法，其特征在于，步骤如下：将藏红花、田旋花、金银花、芦荟、氯化钠、灯心、玄参、决明子、艾叶、鱼腥草、桔梗分别研磨至80～100目，按配比称取混合得到中药粉；将中药粉放入密闭的容器中，通入温度为290～300℃，压力为8～10MPa的水蒸气，处理6～8min，将处理后的中药粉混合液立即放入体积分数为80～85％的乙醇中，中药粉混合液与乙醇的体积比为1:6～8，在超声温度为58～62℃下用300～350r/min的搅拌速率搅拌20～24min，在超声温度为98～102℃下用300～350r/min的搅拌速率搅拌3～5min，过滤去渣，得到滤液，向滤液中加入维生素C、薄荷脑和蒸馏水，搅拌均匀，密封装罐即可。
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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