CN108531339A - 一种功能性药酒及其制备工艺 - Google Patents
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Abstract
一种功能性药酒及其制备工艺,属于保健酒制备技术领域,包括以下原料:米酒120‑200mL、中药提取液22‑30mL及去离子水6‑10mL;所述的中药提取液采用以下重量的中药进行提取:黄精6‑10g、山茱萸5‑8g、高良姜5‑8g、丁香1‑2g、肉桂1‑2g、砂仁1‑2g、葛根2‑4g、太子参2‑4g、川明参2‑4g、何首乌2‑4g、天麻2‑4g、莲子2‑4g、茯苓2‑4g。本发明在配方上,开创性的将黄精、山茱萸等其它中药材组合到一起使用,开发出黄精山茱萸酒新配方。本发明制得的保健酒质量稳定、口感佳、具有优良的保健效果。
Description
技术领域
本发明属于保健酒制备技术领域,具体涉及一种功能性药酒及其制备工艺。
背景技术
保健酒,顾名思义,就是指喝后对人体有营养价值并能起到保健作用的酒。保健酒是以不同的原辅料与基酒按照特定的工艺研制而成,而要研发高质量的保健酒产品一直是许多科研工作者和保健酒公司梦寐以求的事情。当然,研发生产高质量的保健酒产品并不是简单的事情,它不仅工作量大,而且非常复杂,需要做大量的比较性影响配制酒的感官最重要的两个因素是:药材的配比和基酒的种类。
另外,目前保健酒的生产技术科技含量低,产品更新换代速度慢;产品大同小异,差异化小,缺乏卖点和新颖性;一些产品沉淀、失光及口味差等。今天随着科学技术的进步,从中药浸酒的传统工艺的基础上已发展到利用萃取、浸提和生物工程等现代化手段,提取中药中的有效成份制成高含量的功能型保健酒。但是保健酒仍然处于快速成长阶段,市面上的产品普遍质量不高,保健效果有待提升。
发明内容
为了解决现有技术中存在的问题,本发明提供了一种功能性药酒及其制备工艺,可以制得高品质的药酒,且口感醇正、具有优良的保健效果。
本发明采用以下技术方案:
一种功能性药酒,包括以下原料:米酒120-200mL、中药提取液22-30mL及去离子水6-10mL;所述的中药提取液采用以下重量的中药进行提取:黄精6-10g、山茱萸5-8g、高良姜5-8g、丁香1-2g、肉桂1-2g、砂仁1-2g、葛根2-4g、太子参2-4g、川明参2-4g、何首乌2-4g、天麻2-4g、莲子2-4g、茯苓2-4g。
优选的,所述的米酒的酒精度为50%voL。
一种功能性药酒的制备工艺,包括以下步骤:
步骤一:用破碎机将所需中药进行破碎,精确称取,置于容器中,并按料液比1:9加入体积浓度70%乙醇溶液,容器置于88℃水浴锅内加热回流提取2h,重复提取3次,将3次提取液合并,经真空过滤后得到澄清液,然后用旋转蒸发仪浓缩至15-20mL,得初提取液,初提取液放于4℃下备用,过滤后的药渣于60℃下恒温烘干备用;
步骤二:将烘干后的药渣按料液比1:9加入去离子水,在发酵条件为温度32℃、酵母接种量0.5%、初始糖度18%、pH值4、发酵时间7d的条件下进行发酵,发酵完成后,在75℃、25min条件下进行灭菌处理,然后用真空抽滤装置进行过滤,再采用离心装置进行澄清处理,然后将澄清液用旋转蒸发仪浓缩至7-10mL,得药渣提取液,并放置于4℃下备用;
步骤三:将初提取液和药渣提取液合并,混合均匀得中药提取液;
步骤四:将中药提取液注入容器中,不停搅拌,并加120-200mL米酒,同时加入6-10mL去离子水,充分摇匀,静置30min,然后再次充分摇匀,再静置30min,再次充分摇匀,然后用真空抽滤装置进行过滤,收集滤液再采用离心装置进行澄清处理。
优选的,所述的步骤四中离心后再采用超滤。
进一步优选的,所述的超滤截留分子量分别为500-1000。
本发明的有益效果在于:
1)本发明在配方上,开创性的将黄精、山茱萸等其它中药材组合到一起使用,开发出黄精山茱萸酒新配方。
2)本发明制得的保健酒质量稳定、口感佳、具有优良的保健效果。
3)本发明特别采用黄精作为原料,具有补脾润肺,益气养阴的功能,常用于治疗阴虚肺燥、干咳、肾虚、内热消渴以及脾胃虚弱等症状。现代药理研究证明了黄精有增强免疫力、降血糖、降血脂、抗菌、抗肿瘤、抗病毒等作用,在研制药物和开发保健品方面具有着广泛的应用前景。
具体实施方式
以下结合实施例,对本发明中的技术方案进行清楚、完整地描述。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
一种功能性药酒,包括以下原料:米酒120mL、中药提取液22mL及去离子水6mL;所述的中药提取液采用以下重量的中药进行提取:黄精6g、山茱萸5g、高良姜5g、丁香1g、肉桂1g、砂仁1g、葛根2g、太子参2g、川明参2g、何首乌2g、天麻2g、莲子2g、茯苓2g。
所述的米酒的酒精度为50%voL。
一种功能性药酒的制备工艺,包括以下步骤:
步骤一:用破碎机将所需中药进行破碎,精确称取,置于容器中,并按料液比1:9加入体积浓度70%乙醇溶液,容器置于88℃水浴锅内加热回流提取2h,重复提取3次,将3次提取液合并,经真空过滤后得到澄清液,然后用旋转蒸发仪浓缩至15mL,得初提取液,初提取液放于4℃下备用,过滤后的药渣于60℃下恒温烘干备用;
步骤二:将烘干后的药渣按料液比1:9加入去离子水,在发酵条件为温度32℃、酵母接种量0.5%、初始糖度18%、pH值4、发酵时间7d的条件下进行发酵,发酵完成后,在75℃、25min条件下进行灭菌处理,然后用真空抽滤装置进行过滤,再采用离心装置进行澄清处理,然后将澄清液用旋转蒸发仪浓缩至7mL,得药渣提取液,并放置于4℃下备用;
步骤三:将初提取液和药渣提取液合并,混合均匀得中药提取液;
步骤四:将中药提取液注入容器中,不停搅拌,并加120mL米酒,同时加入6mL去离子水,充分摇匀,静置30min,然后再次充分摇匀,再静置30min,再次充分摇匀,然后用真空抽滤装置进行过滤,收集滤液再采用离心装置进行澄清处理。
所述的步骤四中离心后再采用超滤,所述的超滤截留分子量分别为500-1000。
实施例2
一种功能性药酒,包括以下原料:米酒200mL、中药提取液30mL及去离子水10mL;所述的中药提取液采用以下重量的中药进行提取:黄精10g、山茱萸8g、高良姜8g、丁香2g、肉桂2g、砂仁2g、葛根4g、太子参4g、川明参4g、何首乌4g、天麻4g、莲子4g、茯苓4g。
所述的米酒的酒精度为50%voL。
一种功能性药酒的制备工艺,包括以下步骤:
步骤一:用破碎机将所需中药进行破碎,精确称取,置于容器中,并按料液比1:9加入体积浓度70%乙醇溶液,容器置于88℃水浴锅内加热回流提取2h,重复提取3次,将3次提取液合并,经真空过滤后得到澄清液,然后用旋转蒸发仪浓缩至20mL,得初提取液,初提取液放于4℃下备用,过滤后的药渣于60℃下恒温烘干备用;
步骤二:将烘干后的药渣按料液比1:9加入去离子水,在发酵条件为温度32℃、酵母接种量0.5%、初始糖度18%、pH值4、发酵时间7d的条件下进行发酵,发酵完成后,在75℃、25min条件下进行灭菌处理,然后用真空抽滤装置进行过滤,再采用离心装置进行澄清处理,然后将澄清液用旋转蒸发仪浓缩至10mL,得药渣提取液,并放置于4℃下备用;
步骤三:将初提取液和药渣提取液合并,混合均匀得中药提取液;
步骤四:将中药提取液注入容器中,不停搅拌,并加120-200mL米酒,同时加入10mL去离子水,充分摇匀,静置30min,然后再次充分摇匀,再静置30min,再次充分摇匀,然后用真空抽滤装置进行过滤,收集滤液再采用离心装置进行澄清处理。
上面对本发明进行了示例性描述,显然本发明具体实现并不受上述方式的限制,只要采用了本发明的方法构思和技术方案进行的各种非实质性的改进,或未经改进将本发明的构思和技术方案直接应用于其它场合的,均在本发明的保护范围之内。本发明的保护范围应该以权利要求书所限定的保护范围为准。
Claims (7)
1.一种功能性药酒,其特征在于,包括以下原料:米酒120-200mL、中药提取液22-30mL及去离子水6-10mL;所述的中药提取液采用以下重量的中药进行提取:黄精6-10g、山茱萸5-8g、高良姜5-8g、丁香1-2g、肉桂1-2g、砂仁1-2g、葛根2-4g、太子参2-4g、川明参2-4g、何首乌2-4g、天麻2-4g、莲子2-4g、茯苓2-4g。
2.根据权利要求1所述的一种功能性药酒,其特征在于,包括以下原料:米酒120mL、中药提取液22mL及去离子水6mL;所述的中药提取液采用以下重量的中药进行提取:黄精6g、山茱萸5g、高良姜5g、丁香1g、肉桂1g、砂仁1g、葛根2g、太子参2g、川明参2g、何首乌2g、天麻2g、莲子2g、茯苓2g。
3.根据权利要求1所述的一种功能性药酒,其特征在于,包括以下原料:米酒200mL、中药提取液30mL及去离子水10mL;所述的中药提取液采用以下重量的中药进行提取:黄精10g、山茱萸8g、高良姜8g、丁香2g、肉桂2g、砂仁2g、葛根4g、太子参4g、川明参4g、何首乌4g、天麻4g、莲子4g、茯苓4g。
4.根据权利要求1所述的一种功能性药酒,其特征在于:所述的米酒的酒精度为50%voL。
5.一种如权利要求1-4任一项所述的功能性药酒的制备工艺,其特征在于,包括以下步骤:
步骤一:用破碎机将所需中药进行破碎,精确称取,置于容器中,并按料液比1:9加入体积浓度70%乙醇溶液,容器置于88℃水浴锅内加热回流提取2h,重复提取3次,将3次提取液合并,经真空过滤后得到澄清液,然后用旋转蒸发仪浓缩至15-20mL,得初提取液,初提取液放于4℃下备用,过滤后的药渣于60℃下恒温烘干备用;
步骤二:将烘干后的药渣按料液比1:9加入去离子水,在发酵条件为温度32℃、酵母接种量0.5%、初始糖度18%、pH值4、发酵时间7d的条件下进行发酵,发酵完成后,在75℃、25min条件下进行灭菌处理,然后用真空抽滤装置进行过滤,再采用离心装置进行澄清处理,然后将澄清液用旋转蒸发仪浓缩至7-10mL,得药渣提取液,并放置于4℃下备用;
步骤三:将初提取液和药渣提取液合并,混合均匀得中药提取液;
步骤四:将中药提取液注入容器中,不停搅拌,并加120-200mL米酒,同时加入6-10mL去离子水,充分摇匀,静置30min,然后再次充分摇匀,再静置30min,再次充分摇匀,然后用真空抽滤装置进行过滤,收集滤液再采用离心装置进行澄清处理。
6.根据权利要求5所述的一种功能性药酒的制备工艺,其特征在于:所述的步骤四中离心后再采用超滤。
7.根据权利要求6所述的一种功能性药酒的制备工艺,其特征在于:所述的超滤截留分子量分别为500-1000。
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