CN112076197A - 一种感冒颗粒剂制备方法 - Google Patents

一种感冒颗粒剂制备方法 Download PDF

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CN112076197A
CN112076197A CN202010971325.XA CN202010971325A CN112076197A CN 112076197 A CN112076197 A CN 112076197A CN 202010971325 A CN202010971325 A CN 202010971325A CN 112076197 A CN112076197 A CN 112076197A
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granules
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张兰
付建家
付立家
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Beijing Asia East Bio Pharmaceutical Co Ltd
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4402Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 2, e.g. pheniramine, bisacodyl
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/00Medicinal preparations containing organic active ingredients
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • A61K31/522Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
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    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1617Organic compounds, e.g. phospholipids, fats
    • A61K9/1623Sugars or sugar alcohols, e.g. lactose; Derivatives thereof; Homeopathic globules
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1682Processes
    • A61K9/1694Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system

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  • Medicinal Preparation (AREA)
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Abstract

本发明公开了一种感冒颗粒剂制备方法,包括:对蔗糖粉和对乙酰氨基酚预混粉进行过筛,过筛后加入混合槽进行干混;称取浸膏,存放于浸膏桶;把咖啡因和扑尔敏倒入烧杯,加开水溶解倒入浸膏桶,烧杯加开水清洗倒入浸膏桶,对浸膏进行搅拌;搅拌后,浸膏加入槽型混合机中,边搅拌边加入,浸膏加入后,取500ml纯化水对浸膏桶进行清洗,清洗后的水加入槽型混合机进行;观察湿混软材性状,加入乙醇进行颜色调试;用打粒网进行打粒,打出颗粒后,在物料盘中对颗粒进行定型2‑3分钟后,吸入干燥机中进行干燥;整粒。本发明的制作方法简单、成本低,使用本发明方法制备的颗粒结实,均匀度高,颗粒载药均匀,载药量大,可控。

Description

一种感冒颗粒剂制备方法
技术领域
本发明涉及颗粒剂制备技术领域,具体是指一种感冒颗粒剂制备方法。
背景技术
中药或植物药颗粒的传统制备方法是将中药或植物药或其提取物采用干法或湿法制成一定粒度的颗粒状物质,供患者使用时用水冲服或吞服。由于中药或植物药浸膏粘度较高,传统颗粒的制备方法大多存在颗粒的载药量低、外观不美观、颗粒均匀度差、不结实等问题。因此提出一种新的感冒颗粒剂制备方法
发明内容
本发明要解决的技术问题是克服以上技术缺陷,提供一种感冒颗粒剂制备方法。
为了达到上述发明目的,本发明采用的技术方案为:一种感冒颗粒剂制备方法,包括以下步骤:
(1)对蔗糖粉和对乙酰氨基酚预混粉进行过筛,过筛后加入混合槽进行干混;
(2)称取浸膏,存放于浸膏桶;
(3)把咖啡因和扑尔敏倒入烧杯,加入200ml的开水进行溶解,溶解后倒入浸膏桶,烧杯加入200ml开水进行清洗,清洗后溶液倒入浸膏桶,再取500-600ml纯化水分两次对烧杯进行清洗后加入浸膏桶中,对浸膏进行搅拌;
(4)搅拌后,浸膏加入槽型混合机中,边搅拌边加入,浸膏加入后,取500ml纯化水对浸膏桶进行清洗,清洗后的水加入槽型混合机进行;
(5)观察湿混软材性状,加入乙醇进行颜色调试;
(6)用打粒网进行打粒,打出颗粒后,在物料盘中对颗粒进行定型2-3分钟后,吸入干燥机中进行干燥;
(7)整粒。
进一步的,步骤(1)中过筛目数为40目,干混时间为5-10分钟。
进一步的,步骤(3)中搅拌持续不间断时间为10-15分钟。
进一步的,步骤(4)中湿混时间为15-20分钟。
进一步的,步骤(5)中加入55%乙醇500-800ml进行颜色调试,加入乙醇后混合时间为5-10分钟。
进一步的,步骤(6)中打粒网为16目。
本发明的有益效果为:本发明的制作方法简单、成本低,使用本发明方法制备的颗粒结实,均匀度高,颗粒载药均匀,载药量大,可控。
具体实施方式
下面将结合本发明实施例,对本发明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。
一种感冒颗粒剂制备方法,包括以下步骤:
(1)对车间现有蔗糖粉和对乙酰氨基酚预混粉进行过筛,过筛目数40目,过筛后加入混合槽进行干混,干混时间5-10分钟;
(2)按工艺要求称取浸膏,存放于浸膏桶;
(3)溶咖啡因、扑尔敏,把咖啡因和扑尔敏倒入烧杯,加入200ml的开水进行溶解,溶解后加入浸膏桶,烧杯加入200ml开水进行清洗,清洗后溶液加入浸膏桶,再取500-600ml纯化水分两次对烧杯进行清洗后加入浸膏桶中,可以增加软材粘度,使颗粒更加结实,对浸膏进行搅拌,搅拌时间10-15分钟,搅拌期间不能停止;
(4)搅拌后,浸膏均匀加入槽型混合机中,边搅拌边加入浸膏,浸膏加入后,取500ml纯化水对浸膏桶进行清洗,清洗后的水加入混合槽,湿混时间15-20分钟;
(5)观察湿混软材性状,加入500-800ml55%乙醇,进行颜色调试,加入乙醇后混合时间5-10分钟;
(6)用16目打粒网进行打粒,打出颗粒后,在物料盘中对颗粒进行定型2-3分钟后,吸入干燥机中进行干燥;
(7)整粒。整粒后,合格颗粒数量在70kg左右,大颗粒1kg左右,细粉量3kg左右。每锅产出大颗粒,经摇摆颗粒机整粒后,加入下一锅湿混后制粒;产出细粉,最终进行制粒、总混并进行含量及均匀度检测。
以上对本发明及其实施方式进行了描述,这种描述没有限制性,只是本发明的实施方式之一,实际的实施方式并不局限于此。总而言之如果本领域的普通技术人员受其启示,在不脱离本发明创造宗旨的情况下,不经创造性的设计出与该技术方案相似的实施例,均应属于本发明的保护范围。

Claims (6)

1.一种感冒颗粒剂制备方法,其特征在于:包括以下步骤:
(1)对蔗糖粉和对乙酰氨基酚预混粉进行过筛,过筛后加入混合槽进行干混;
(2)称取浸膏,存放于浸膏桶;
(3)把咖啡因和扑尔敏倒入烧杯,加入200ml的开水进行溶解,溶解后倒入浸膏桶,烧杯加入200ml开水进行清洗,清洗后溶液倒入浸膏桶,再取500-600ml纯化水分两次对烧杯进行清洗后加入浸膏桶中,对浸膏进行搅拌;
(4)搅拌后,浸膏加入槽型混合机中,边搅拌边加入,浸膏加入后,取500ml纯化水对浸膏桶进行清洗,清洗后的水加入槽型混合机进行;
(5)观察湿混软材性状,加入乙醇进行颜色调试;
(6)用打粒网进行打粒,打出颗粒后,在物料盘中对颗粒进行定型2-3分钟后,吸入干燥机中进行干燥;
(7)整粒。
2.根据权利要求1所述的一种感冒颗粒剂制备方法,其特征在于:步骤(1)中过筛目数为40目,干混时间为5-10分钟。
3.根据权利要求1所述的一种感冒颗粒剂制备方法,其特征在于:步骤(3)中搅拌持续不间断时间为10-15分钟。
4.根据权利要求1所述的一种感冒颗粒剂制备方法,其特征在于:步骤(4)中湿混时间为15-20分钟。
5.根据权利要求1所述的一种感冒颗粒剂制备方法,其特征在于:步骤(5)中加入55%乙醇500-800ml进行颜色调试,加入乙醇后混合时间为5-10分钟。
6.根据权利要求1所述的一种感冒颗粒剂制备方法,其特征在于:步骤(6)中打粒网为16目。
CN202010971325.XA 2020-09-16 2020-09-16 一种感冒颗粒剂制备方法 Pending CN112076197A (zh)

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102614220A (zh) * 2012-04-14 2012-08-01 辽宁王牌速效制药有限公司 氨咖黄敏胶囊内容物功能微丸的制备方法
CN102727625A (zh) * 2011-03-30 2012-10-17 赵文志 一种治疗感冒的复方感冒灵片改进制剂
CN104383332A (zh) * 2014-11-25 2015-03-04 华润三九(郴州)制药有限公司 一种复方感冒灵颗粒及其制备方法

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102727625A (zh) * 2011-03-30 2012-10-17 赵文志 一种治疗感冒的复方感冒灵片改进制剂
CN102614220A (zh) * 2012-04-14 2012-08-01 辽宁王牌速效制药有限公司 氨咖黄敏胶囊内容物功能微丸的制备方法
CN104383332A (zh) * 2014-11-25 2015-03-04 华润三九(郴州)制药有限公司 一种复方感冒灵颗粒及其制备方法

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