CN108670996A - 人参鲜提冷冻干燥粉末饮片 - Google Patents
人参鲜提冷冻干燥粉末饮片 Download PDFInfo
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- CN108670996A CN108670996A CN201810733206.3A CN201810733206A CN108670996A CN 108670996 A CN108670996 A CN 108670996A CN 201810733206 A CN201810733206 A CN 201810733206A CN 108670996 A CN108670996 A CN 108670996A
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/25—Araliaceae (Ginseng family), e.g. ivy, aralia, schefflera or tetrapanax
- A61K36/258—Panax (ginseng)
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/10—Preparation or pretreatment of starting material
- A61K2236/13—Preparation or pretreatment of starting material involving cleaning, e.g. washing or peeling
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/10—Preparation or pretreatment of starting material
- A61K2236/15—Preparation or pretreatment of starting material involving mechanical treatment, e.g. chopping up, cutting or grinding
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/30—Extraction of the material
- A61K2236/33—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones
- A61K2236/331—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones using water, e.g. cold water, infusion, tea, steam distillation, decoction
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/30—Extraction of the material
- A61K2236/39—Complex extraction schemes, e.g. fractionation or repeated extraction steps
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/50—Methods involving additional extraction steps
- A61K2236/51—Concentration or drying of the extract, e.g. Lyophilisation, freeze-drying or spray-drying
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Abstract
本发明公布了一种“人参鲜提冷冻干燥粉末饮片”,其主要特征在于:人参药材采收后,趁鲜洗涤、切片、榨汁、提取,提取液浓缩后,冻结、真空冷冻干燥,再经粉碎、过筛后真空包装。冷冻粉末饮片的含水量少于12%,含人参皂苷Rg1(C42H72O14)和人参皂苷Re(C48H82O18)的总量不得低于0.40%。本饮片质量稳定,既可以入汤剂煎煮,也可以直接入丸剂、散剂、片剂、膏滋,利于携带,临床使用方便。
Description
技术领域
本发明属于中药饮片技术领域,尤其属于中药人参饮片的加工领域。
背景技术
中药人参为五加科植物人参Panaxginseng C.A.Mey.的干燥根和根茎。常在秋季采挖,洗净后晒干或烘干。传统生晒人参饮片的加工方法为,将在产地晒干或者烘干的人参药材,去芦头,分档,加水润软,或者烘软后切片,干燥,包装。这样的饮片体积大,卫生学标准差,易于受潮、长霉,带有虫卵,不利于保管,储存和运输成本高。此外,这样的饮片质量稳定性差,临床疗效难以保障,病人服用不方便,起效慢。因此,开发一种质量稳定可靠、储存/运输成本低、利于保管、携带和使用方便、起效快的新型人参饮片,势在必行。目前市场有人参超微粉饮片和人参浓缩颗粒饮片,但两者都是以传统人参饮片为原料,其质量决定于人参饮片的质量,且超微饮片不能解决药材污染的问题;浓缩颗粒只能提取出水溶性成分。
发明内容
本发明公布了一种“人参鲜提喷雾干燥粉末饮片”,其主要特征在于:人参药材采收后,净选,除去杂质,在6小时内趁鲜洗净泥沙,并于24小时内切成2~5mm厚的片,压榨取汁。所得药渣中加1~5倍重量的水,搅拌5~30分钟,过滤,药渣再压榨取汁。第二次所得药渣中再加入5~10倍重量的水,煮沸10~30分钟提取,趁热过滤,药渣再次榨汁,收集药汁。合并上述药汁,减压浓缩,温度设定为50~70℃,浓缩至相对密度为1.05~1.20的清膏。将此清膏置于-20~-80℃冰箱内冻结12~24小时,取出后于-20~-40℃真空冷冻干燥,收集冻干物,再于60℃真空干燥箱内干燥至干燥物含水量少于12%,粉碎,过60目筛,真空包装,即得成品。饮片成品含人参皂苷Rg1(C42H72O14)和人参皂苷Re(C48H82O18)的总量不得低于0.40%。 本饮片临床一般使用量为1~3g。此饮片既可入汤剂煎服或冲服,也可直接入丸剂、散剂、胶囊剂及片剂中,从而大大提高了临床使用的便捷性和顺应性,有利于临床急症的治疗。
具体实施例
将人参药材采收后,净选,除去杂质和芦头,在6小时内趁鲜洗净泥沙,并于24小时内切成3mm厚的片,压榨取汁。所得药渣中加5倍重量的水,搅拌30分钟,过滤,药渣再压榨取汁。第二次所得药渣中再加入8倍重量的水,煮沸20分钟提取,趁热过滤,药渣再次榨汁,收集药汁。合并上述药汁,减压浓缩,温度为设定为70℃,浓缩至相对密度为1.20清膏。将所得的清膏于-80℃冰箱冻结24小时,再于-40℃真空冷冻干燥。收集冻干物,于60℃真空干燥至干燥物含水量低于12%,取出,粉碎,过60目筛,真空包装,即得成品。饮片成品含人参皂苷Rg1(C42H72O14)和人参皂苷Re(C48H82O18)的总量不得低于0.40%。
Claims (2)
1.一种人参鲜提冷冻干燥粉末饮片,其主要特征在于:人参药材采收后,净选,6小时内趁鲜洗净泥沙,24小时内切成2~5mm厚的片;压榨取汁,药渣中加1~5倍重量的水,搅拌5~30分钟,过滤,药渣压榨取汁;所得药渣中再加入5~10倍重量的水,煮沸10~30分钟,趁热过滤,药渣再榨汁,收集药汁;合并上述药汁,减压浓缩,温度为50~70℃,浓缩至相对密度为1.05~1.20的清膏;将此清膏冻结后真空冷冻干燥,收集冻干物,控制干燥物含水量为10%以内,粉碎,过60目筛,真空包装,即得成品;成品含人参皂苷Rg1(C42H72O14)和人参皂苷Re(C48H82O18)的总量不得低于0.40%。
2.根据权利要求1所述的人参鲜提冷冻干燥粉末饮片,其主要特征在于:临床一般使用量为1~3g,此饮片既可入汤剂煎服,也可直接入丸剂、散剂、胶囊剂及片剂中。
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN109999072A (zh) * | 2019-05-16 | 2019-07-12 | 康美(北京)药物研究院有限公司 | 一种鲜人参活性物质的制备方法 |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN109999072A (zh) * | 2019-05-16 | 2019-07-12 | 康美(北京)药物研究院有限公司 | 一种鲜人参活性物质的制备方法 |
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