CN107441194A - 一种温经散寒伸筋草药浴液及其制备方法 - Google Patents

一种温经散寒伸筋草药浴液及其制备方法 Download PDF

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CN107441194A
CN107441194A CN201710727842.0A CN201710727842A CN107441194A CN 107441194 A CN107441194 A CN 107441194A CN 201710727842 A CN201710727842 A CN 201710727842A CN 107441194 A CN107441194 A CN 107441194A
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廖艳卿
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Abstract

本发明公开了温经散寒伸筋草药浴液,其由以下重量份的中草药原料制成:伸筋草25~35份,威灵仙15~25份,续断10~20份,麻黄10~15份,桂枝10~20份,当归10~15份,红花3~6份,川乌10~15份,草乌10~15份,乳香5~12份,没药5~10份,川芎5~10份。本发明还公开了温经散寒伸筋草药浴液的制备方法,通过原料粉碎酶解、微生物发酵、超声波辅助水浸提和超声波辅助醇浸提为主要步骤制成。本发明中草药原料来源广,价格低廉,配方科学合理,制备工艺简单,提取中草药功能性成分高,产品安全环保,对人体无任何副作用,消脂瘦身效果显著。

Description

一种温经散寒伸筋草药浴液及其制备方法
技术领域
本发明公开了一种药浴液,尤其涉及一种温经散寒伸筋草药浴液及其制备方法,属中医中药领域。
背景技术
风寒湿痹是风、寒、湿三气外邪侵袭人体经络,造成气血闭阻不畅,引起关节、肢体等处出现酸、痛、麻、重及屈伸不利等症状。可见于现代医学诊断的风湿热、风湿性关节炎、类风湿性关节炎、纤维组织炎及神经痛等。
正气不足是痹病的内在因素和病变的基础。外感风寒湿邪,多因居处潮湿,涉水冒雨,或睡卧当风,或冒雾露,气候变化,冷热交错等原因,以致风寒湿邪乘虚侵袭人体所致。现代人不正当生活方式如夏天长时间呆在空调房,长时间吹风扇,大量喝冷饮吃凉菜,这些都能引起风寒湿痹。
风寒湿痹症可以采用中西药对症处理,如疼痛时可服一些解热镇痛药;麻木者可选用B族维生素类药物;关节肿胀有积液者可给予局部抽取积液或局部封闭等疗法。但这些治疗方法均不理想,病情易复发。或是用理疗的方法,直流电药物离子导入法充分发挥了药物的作用,但因导入药物为液体,易挥发,药效不持久,限制了该方法的治疗效果。其他可采用紫外线,红外线,微波,激光等治疗方法都有一定的效果,但是由于该症较为顽劣,采取一般的治疗方法多数不易治愈,造成病程长、花费多、康复慢,给患者和家属带来较重的负担。
药浴对人体具有独到功效,在中国已有几千年的历史,自古以来一直受医学界重视。药浴法是外治法之一,即用药液或含有药液水洗浴全身或局部的一种方法,其形式多种多样。药浴作用机理概言之,药物作用于全身肌表、局部、患处,并经吸收,循行经络血脉,内达脏腑,由表及里,因而产生效应。药浴洗浴,可起到疏通经络、活血化淤、驱风散寒、清热解毒、消肿止痛、调整阴阳、协调脏腑、通行气血、濡养全身等养生功效。药浴避免了药物对脾胃的刺激和对肝脏的损害,使药物有效成分通过皮肤吸收而发挥功效,是防治各种慢性疾病和养生保健的理想方法。
中草药是我国传统文化的瑰宝,在实践中证明多种中草药具有促进新陈代谢,改善血液循环,补肝强肾,问津活络,祛风散寒,解肌除湿,强筋健骨等功效,因此,将中草药应用于温经散寒对于提高国民生活质量,保障生活安全具有十分重要的意义,但目前中草药减肥药浴在温经散寒,治疗风寒湿痹应用尚未实现规模化和产业化,主要问题是中草药配伍不合理、功能成分提取率低、难以工业化生产、功效不显著等弊端,因此开发新型的温经散寒,治疗风寒湿痹药浴具有重要的现实意义。
发明内容
本发明的目的在于根据现有温经散寒产品存在的上述问题,开发一种温经散寒伸筋草药浴液,使人们通过药浴来促进机体新陈代谢,改善机体血液循环,祛风散寒,解肌除湿,问津活络,补肝强肾,强筋健骨,从根源上祛除病因,让人们远离风寒湿痹的困扰。
为了实现上述目的,本发明采用以下技术方案:
一种温经散寒伸筋草药浴液,由以下重量份的中草药原料制成:伸筋草25~35份,威灵仙15~25份,续断10~20份,麻黄10~15份,桂枝10~20份,当归10~15份,红花3~6份,川乌10~15份,草乌10~15份,乳香5~12份,没药5~10份,川芎5~10份。
本发明温经散寒伸筋草药浴液的制备方法,包括如下步骤:
(1)备料:剔除中草药原料中的杂质,霉变和生虫原料后,按照上述比例备料;
(2)原料处理:将中草药原料清洗干净,在50~75 ℃下,鼓风烘干后,粉碎机粉碎,过60~100目筛,混匀,得复合中草药原料;
(3)酶解:将步骤(2)所得复合中草药原料加水至固液比1:3~5,按1.5~2.0 g/L、1.0~1.5 g/L、2.0~2.5 g/L比例分别添加非淀粉多糖酶、糖化酶、纤维素酶,在600~900 W超声波辅助作用下,在35~50 ℃条件下协同酶解50~75 min;
(4)微生物发酵:向步骤(3)所得酶解浸提液中加入3~5%活化后的双歧杆菌(活菌数≥200亿/ml),厌氧条件下发酵15~20 h,控制发酵温度30~35 ℃;
(5)超声波辅助水浸提:将步骤(4)微生物发酵混合液,加温到85~95 ℃,在600~1000W超声波辅助作用下,浸提40~60 min,浸提结束后,过150~200目滤布得水浸提液。滤渣加2~4倍纯净水,按同样方法进行超声波辅助浸提,过滤得滤液,合并两次提取液即为水浸提液;
(6)超声波辅助乙醇浸提:向步骤(5)所得滤渣中加入3~5倍浓度为50~60%的乙醇,在600~900 W 超声波辅助条件下,浸提40~60 min,浸提温度60~75 ℃;
(7)离心:浸提结束后离心分离固体残渣和醇提液;
(8)浓缩蒸馏:将醇提液减压浓缩蒸馏回收乙醇;
(9)混合:将步骤(8)回收乙醇后的浸提液与步骤(5)水浸提液混合;
(10)过滤:将混合液经硅藻过滤机过滤除去其中的杂质及不溶物即得温经散寒伸筋草药浴液。
本发明提供一种温经散寒伸筋草药浴液,结合配方中各中草药的特性,采用中医辨证理论所研制,配方科学合理,各组分之间协同作用,经长期使用证明本发明对各种风寒湿痹症,包括腰痛,腿痛,颈椎病,肩周炎及股骨头病,椎管狭窄,骨质增生均有良好的疗效。本发明的优势在于:(1)产品使用药浴时药物不需经过体内吸收,将药效直接作用于患处,安全环保,药性平和,对人体无任何副作用;(2)产品具有宜人的中草药清香,使用便捷,使用时只需取本产品按1:300~600比例调入热浴水中,便可进行浸泡洗浴;((3)与药浴粉单纯添加相比,本发明采用原料粉碎酶解、微生物发酵、超声波辅助水浸提和超声波辅助醇浸提为主要制备步骤,提高中草药功能性成分,祛风散寒功效显著;(4)本发明中原料来源广,价格低廉,生产加工工艺简单,适合规模化生产。
具体实施方式
下面通过具体实施方式对本发明做进一步的描述。在本发明中,若非特指,所有百分比均为重量单位,所有设备和原料均可从市场购得或是本行业常用的,下述实施例中的方法,如无特别说明,均为本领域常规方法。
实施例1
一种温经散寒伸筋草药浴液,由以下各组分的中草药原料制成:伸筋草,威灵仙,续断,麻黄,桂枝,当归,红花,川乌,草乌,乳香,没药和川芎。中草药原料中各组分的具体配比如表1所示。
本发明温经散寒伸筋草药浴液的制备方法,包括如下步骤:
(1)备料:剔除中草药原料中的杂质,霉变和生虫原料后,按照上述比例备料;
(2)原料处理:将中草药原料清洗干净,在70 ℃下,鼓风烘干后,粉碎机粉碎,过80目筛,混匀,得复合中草药原料;
(3)酶解:将步骤(2)所得复合中草药原料加水至固液比1:5,按1.6 g/L、1.4 g/L、2.1g/L比例分别添加非淀粉多糖酶、糖化酶、纤维素酶,在800 W超声波辅助作用下,在40 ℃条件下协同酶解65 min;
(4)微生物发酵:向步骤(3)所得酶解浸提液中加入4%活化后的双歧杆菌(活菌数≥200亿/ml),厌氧条件下发酵18 h,控制发酵温度30 ℃;
(5)超声波辅助水浸提:将步骤(4)微生物发酵混合液,加温到86 ℃,在700 W超声波辅助作用下,浸提45 min,浸提结束后,过200目滤布得水浸提液。滤渣加4倍纯净水,按同样方法进行超声波辅助浸提,过滤得滤液,合并两次提取液即为水浸提液;
(6)超声波辅助乙醇浸提:向步骤(5)所得滤渣中加入3倍浓度为58%的乙醇,在600 W超声波辅助条件下,浸提56 min,浸提温度63 ℃;
(7)离心:浸提结束后离心分离固体残渣和醇提液;
(8)浓缩蒸馏:将醇提液减压浓缩蒸馏回收乙醇;
(9)混合:将步骤(8)回收乙醇后的浸提液与步骤(5)水浸提液混合;
(10)过滤:将混合液经硅藻过滤机过滤除去其中的杂质及不溶物即得温经散寒伸筋草药浴液。
实施例2
一种温经散寒伸筋草药浴液,由以下各组分的中草药原料制成:伸筋草,威灵仙,续断,麻黄,桂枝,当归,红花,川乌,草乌,乳香,没药和川芎。中草药原料中各组分的具体配比如表1所示。
本发明温经散寒伸筋草药浴液的制备方法,包括如下步骤:
(1)备料:剔除中草药原料中的杂质,霉变和生虫原料后,按照上述比例备料;
(2)原料处理:将中草药原料清洗干净,在65 ℃下,鼓风烘干后,粉碎机粉碎,过90目筛,混匀,得复合中草药原料;
(3)酶解:将步骤(2)所得复合中草药原料加水至固液比1:4,按1.8 g/L、1.2 g/L、2.3g/L比例分别添加非淀粉多糖酶、糖化酶、纤维素酶,在700 W超声波辅助作用下,在44 ℃条件下协同酶解70 min;
(4)微生物发酵:向步骤(3)所得酶解浸提液中加入3%活化后的双歧杆菌(活菌数≥200亿/ml),厌氧条件下发酵20 h,控制发酵温度32 ℃;
(5)超声波辅助水浸提:将步骤(4)微生物发酵混合液,加温到90 ℃,在800 W超声波辅助作用下,浸提50 min,浸提结束后,过180目滤布得水浸提液。滤渣加3倍纯净水,按同样方法进行超声波辅助浸提,过滤得滤液,合并两次提取液即为水浸提液;
(6)超声波辅助乙醇浸提:向步骤(5)所得滤渣中加入4倍浓度为54%的乙醇,在700 W超声波辅助条件下,浸提52 min,浸提温度68 ℃;
(7)离心:浸提结束后离心分离固体残渣和醇提液;
(8)浓缩蒸馏:将醇提液减压浓缩蒸馏回收乙醇;
(9)混合:将步骤(8)回收乙醇后的浸提液与步骤(5)水浸提液混合;
(10)过滤:将混合液经硅藻过滤机过滤除去其中的杂质及不溶物即得温经散寒伸筋草药浴液。
实施例3
一种温经散寒伸筋草药浴液,由以下各组分的中草药原料制成:伸筋草,威灵仙,续断,麻黄,桂枝,当归,红花,川乌,草乌,乳香,没药,川芎。中草药原料中各组分的具体配比如表1所示。
本发明温经散寒伸筋草药浴液的制备方法,包括如下步骤:
(1)备料:剔除中草药原料中的杂质,霉变和生虫原料后,按照上述比例备料;
(2)原料处理:将中草药原料清洗干净,在55 ℃下,鼓风烘干后,粉碎机粉碎,过70目筛,混匀,得复合中草药原料;
(3)酶解:将步骤(2)所得复合中草药原料加水至固液比1:3,按2.0 g/L、1.0 g/L、2.5g/L比例分别添加非淀粉多糖酶、糖化酶、纤维素酶,在600 W超声波辅助作用下,在48 ℃条件下协同酶解55 min;
(4)微生物发酵:向步骤(3)所得酶解浸提液中加入5%活化后的双歧杆菌(活菌数≥200亿/ml),厌氧条件下发酵16 h,控制发酵温度34 ℃;
(5)超声波辅助水浸提:将步骤(4)微生物发酵混合液,加温到93 ℃,在900 W超声波辅助作用下,浸提55 min,浸提结束后,过160目滤布得水浸提液。滤渣加2~4倍纯净水,按同样方法进行超声波辅助浸提,过滤得滤液,合并两次提取液即为水浸提液;
(6)超声波辅助乙醇浸提:向步骤(5)所得滤渣中加入5倍浓度为52%的乙醇,在800 W超声波辅助条件下,浸提48 min,浸提温度72 ℃;
(7)离心:浸提结束后离心分离固体残渣和醇提液;
(8)浓缩蒸馏:将醇提液减压浓缩蒸馏回收乙醇;
(9)混合:将步骤(8)回收乙醇后的浸提液与步骤(5)水浸提液混合;
(10)过滤:将混合液经硅藻过滤机过滤除去其中的杂质及不溶物即得温经散寒伸筋草药浴液。
表1. 各实施例中草药原料的组成配比
序号 组分 实施例1 实施例2 实施例3
1 伸筋草(份) 28 30 33
2 威灵仙(份) 24 21 19
3 续断(份) 13 16 18
4 麻黄(份) 13 14 11
5 桂枝(份) 17 15 12
6 当归(份) 11 13 12
7 红花(份) 3 4 5
8 川乌(份) 11 13 12
9 草乌(份) 13 11 12
10 乳香(份) 6 8 7
11 没药(份) 8 9 6
12 川芎(份) 7 6 9
13 总和(份) 154 160 156
尽管为达到说明目的,以上所述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 (2)

1.一种温经散寒伸筋草药浴液,其特征在于,由以下按重量份的中草药原料制成:伸筋草25~35份,威灵仙15~25份,续断10~20份,麻黄10~15份,桂枝10~20份,当归10~15份,红花3~6份,川乌10~15份,草乌10~15份,乳香5~12份,没药5~10份,川芎5~10份。
2.一种如权利要求1所述的温经散寒伸筋草药浴液的制备方法,其特征在于,包括以下步骤:
(1)备料:剔除中草药原料中的杂质,霉变和生虫原料后,按照上述比例备料;
(2)原料处理:将中草药原料清洗干净,在50~75 ℃下,鼓风烘干后,粉碎机粉碎,过60~100目筛,混匀,得复合中草药原料;
(3)酶解:将步骤(2)所得复合中草药原料加水至固液比1:3~5,按1.5~2.0 g/L、1.0~1.5 g/L、2.0~2.5 g/L比例分别添加非淀粉多糖酶、糖化酶、纤维素酶,在600~900 W超声波辅助作用下,在35~50 ℃条件下协同酶解50~75 min;
(4)微生物发酵:向步骤(3)所得酶解浸提液中加入3~5%活化后的双歧杆菌(活菌数≥200亿/ml),厌氧条件下发酵15~20 h,控制发酵温度30~35 ℃;
(5)超声波辅助水浸提:将步骤(4)微生物发酵混合液,加温到85~95 ℃,在600~1000W超声波辅助作用下,浸提40~60 min,浸提结束后,过150~200目滤布得水浸提液;滤渣加2~4倍纯净水,按同样方法进行超声波辅助浸提,过滤得滤液,合并两次提取液即为水浸提液;
(6)超声波辅助乙醇浸提:向步骤(5)所得滤渣中加入3~5倍浓度为50~60%的乙醇,在600~900 W 超声波辅助条件下,浸提40~60 min,浸提温度60~75 ℃;
(7)离心:浸提结束后离心分离固体残渣和醇提液;
(8)浓缩蒸馏:将醇提液减压浓缩蒸馏回收乙醇;
(9)混合:将步骤(8)回收乙醇后的浸提液与步骤(5)水浸提液混合;
(10)过滤:将混合液经硅藻过滤机过滤除去其中的杂质及不溶物即得温经散寒伸筋草药浴液。
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CN110384783A (zh) * 2018-04-18 2019-10-29 李同春 一种用于薰蒸治病的中药组合物及中药发酵液
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