CN107213200A - 一种辛夷花鲜榨喷雾干燥颗粒饮片及其制备工艺 - Google Patents
一种辛夷花鲜榨喷雾干燥颗粒饮片及其制备工艺 Download PDFInfo
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Abstract
本发明公布了一种辛夷花鲜榨喷雾干燥颗粒饮片及其制备工艺。该工艺在辛夷花药材采收后,净选、淋洗,并趁鲜压榨,滤取药汁。药渣再加水搅拌,过滤压榨。所得药汁合并后减压浓缩,喷雾干燥;浓缩冷凝液分离挥发油,经β‑环糊精包合后,与喷雾干燥物混合,整粒,装袋,真空封装。此法制备的辛夷花颗粒饮片,最大限度的保留了药材中的有效成分。颗粒饮片流动性好,便于储运,方便调剂,质量可控,疗效可靠,对保障中医药临床疗效具有重要的意义。本法的推广实施,将有显著的社会意义和经济效益。
Description
技术领域
本发明属于中药材加工领域,尤其涉及中药辛夷花饮片的加工工艺。
背景技术
中药辛夷花为木兰科植物望春花Magnolia biondii Pamp.、玉兰Magnolia denudata Desr. 或武当玉兰Magnolia sprengeri Pamp.的干燥花蕾。本品具有散风寒,通鼻窍的功效。用于风寒头痛,鼻塞流涕,鼻渊等的治疗。
常用的辛夷花饮片的加工方式为:冬末春初花未开放时采收,除去枝梗,阴干,打包储藏和运输。此类中药饮片,体积庞大,容易污染和霉变,卫生学条件差,质量很难保证,不利于配方调剂和确保其临床疗效。
目前,市场上也有辛夷花药材经过提取后制成的颗粒饮片销售。由于颗粒饮片制备过程中,提取不仅耗时耗能,而且因常用水做溶媒,药材中的非极性有效成分很难被提取出来。此外,由于提取用的辛夷花药材也是干燥并经过长时间储藏的,因此,有效成分的损失也是很大的。为了确保辛夷花药材的临床有效、质量稳定,一种新型的辛夷花饮片及其制备工艺亟待开发。
发明内容
本发明公布了 “一种辛夷花鲜榨喷雾干燥颗粒饮片及其制备工艺”。本工艺可以最大限度的保留辛夷花药材中的极性和非极性有效成分,避免药材在现有的饮片加工和储运过程中引起的有效成分的丢失和药材品质的下降,减少药材受霉菌等的污染,对确保辛夷花饮片的质量稳定和临床安全有效具有重要的意义。
为了实现上述目的,本发明的技术方案为:
在辛夷花采收期采集其地上部分,净选,洗涤后,趁鲜压榨取汁,药渣加入1~3倍量的水,搅拌5~30min,板框压滤机压滤,所得药渣再压榨取汁,合并药汁并用80~200目筛网过滤。将所得的药液,40~80℃减压浓缩,所得相对密度为1.02~1.10的浓缩液喷雾干燥,进风口温度为90~120℃,出风口温度为70~100℃,收集喷干产物并粉碎。同时,收集减压浓缩所得的辛夷花冷凝水,加入1%~5%重量的NaCl,搅拌使溶解,溶液置油水分离器中,于4℃~10℃环境下放置12~48小时,收集上部油层,并往其中加入1%~5%重量的无水Na2SO4,振摇5~10min钟后,25℃以下室温放置1~6小时,过滤,得辛夷花挥发油。将得到的辛夷花挥发油,与1~6倍重量的β-环糊精等量递增法研磨包合,并将包合物与上述喷雾干产物混合均匀,湿法制粒,60~75℃下干燥4~8小时,整粒,真空包装即可。
在产品包装袋的标签上,印刷上品名、药用部位、种植地、生产商、生产日期、主要成分含量、性味归经、功能主治、用法用量、毒副作用及禁忌证等信息。袋内附上辛夷花的薄层鉴别图谱和/或高效液相特征图谱,作为产品的“身份证”。此外,在产品的包装袋上,印有二维码,通过扫描可以链接获取产品的原植物照片、药材照片、饮片照片、性状及显微鉴别特征等信息。
本发明的有益之处在于:
新鲜辛夷花药材净选洗涤后直接压榨、过滤、减压浓缩、喷雾干燥、分离挥发油、环糊精包合、混合制粒,所得到的颗粒饮片,可以最大限度地完整保留药材中的有效成分,特别是对保留挥发性有效成分,具有重要意义。 这种饮片体积较之于传统饮片体积大大地减小,质量更加稳定,颗粒流动性好,利于储运和临床调剂,具有十分显著的社会意义和经济意义。
具体实施方式
实施例1
将新鲜采集的辛夷花药材,净选,用水淋洗,趁鲜用压榨机压榨,取汁。所得药渣加2倍量的饮用水,搅拌20min,板框压滤机压榨取汁。所得药渣再用压榨机榨取药汁。将上述3次药汁合并,减压浓缩,温度设定为65℃。在浓缩液相对密度为1.05时,喷雾干燥,进风口温度为110℃,出风口温度为80℃,收集干燥物并粉碎。另外,将减压浓缩时收集的辛夷花冷凝水,加入重量5%的NaCl,搅拌使溶解。将此溶液放置于油水分离器中,并于10℃环境中静置24小时,分离收集上层挥发油。往此挥发油中加入2%重量的无水Na2SO4,振摇10min钟后,25℃以下室温放置6小时,过滤,得辛夷花挥发油。将此挥发油与2倍重量的β-环糊精研磨包合,再与上述辛夷花喷雾干燥粉碎物混合均匀,制软材,制粒,于65℃下,干燥8小时,整粒,过筛,收集能通过24目筛,且不能通过60筛的颗粒,装袋,1kg/袋,加入袋装干燥剂、抗氧化剂,真空封装,贴签即可。
实施例2
将新鲜采集的辛夷花药材,净选,用水淋洗,趁鲜用压榨机压榨,取汁。所得药渣加3倍量的饮用水,搅拌30min,板框压滤机压榨取汁。所得药渣再用压榨机榨取药汁。将上述3次药汁合并,减压浓缩,温度设定为60℃。在浓缩液相对密度为1.08时,喷雾干燥,进风口温度为120℃,出风口温度为90℃,收集干燥物并粉碎。另外,将减压浓缩时收集的辛夷花冷凝水,加入重量3%的NaCl,搅拌使溶解。将此溶液放置于油水分离器中,并于10℃环境中静置12小时,分离收集上层挥发油。往此挥发油中加入5%重量的无水Na2SO4,振摇10min钟后,25℃以下室温放置12小时,过滤,得辛夷花挥发油。将此挥发油与5倍重量的β-环糊精用等量递增法研磨包合,再与上述辛夷花喷雾干燥粉碎物混合均匀,制软材,制粒,于70℃下,干燥6小时,整粒,过筛,收集能通过24目筛,且不能通过60筛的颗粒,装袋,1kg/袋,加入袋装干燥剂、抗氧化剂,真空封装,贴签即可。
以上实施例,仅为说明本项发明的技术思想,不能凭此限定本发明的保护范围 凡是按照本发明提出的技术思想,在技术方案基础上所做的任何改动,均落入本发明保护的范围之内。
Claims (4)
1.一种辛夷花鲜榨喷雾干燥颗粒饮片及其制备工艺,其特征在于:在辛夷花采收后,净选,洗涤,趁鲜压榨取汁,药渣加入1~3倍量的水,搅拌5~30min,板框压滤机压滤,所得药渣再压榨取汁,合并药汁并用80~200目筛网过滤。
2.根据权利要求1所述的一种辛夷花鲜榨喷雾干燥粉末饮片及其制备工艺,其特征在于:将权利要求1中所得的药液,40~80℃减压浓缩,所得相对密度为1.02~1.10的浓缩液喷雾干燥,进风口温度为90~120℃,出风口温度为70~100℃,收集喷干产物并粉碎。
3.根据权利要求1所述的一种辛夷花鲜榨喷雾干燥粉末饮片及其制备工艺,其特征在于:收集权利要求2中的减压浓缩所得的辛夷花冷凝水,加入1%~5%重量的NaCl,搅拌使溶解,溶液置油水分离器中,于4℃~10℃环境下放置12~48小时,收集上部油层,并往其中加入1%~5%重量的无水Na2SO4,振摇5~10min钟后,25℃以下室温放置1~6小时,过滤,得辛夷花挥发油。
4.根据权利要求1所述的一种辛夷花鲜榨喷雾干燥粉末饮片及其制备工艺,其特征在于:将权利要求3中得到的辛夷花挥发油,与1~6倍重量的β-环糊精等量递增法研磨包合,并将包合物与权利要求2中的喷雾干产物混合均匀,湿法制粒,60~75℃下干燥4~8小时,整粒,真空包装即可。
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