CN101474270B - Cough-relieving tablet - Google Patents
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- CN101474270B CN101474270B CN2008100257369A CN200810025736A CN101474270B CN 101474270 B CN101474270 B CN 101474270B CN 2008100257369 A CN2008100257369 A CN 2008100257369A CN 200810025736 A CN200810025736 A CN 200810025736A CN 101474270 B CN101474270 B CN 101474270B
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- 206010011224 Cough Diseases 0.000 title claims abstract description 15
- 239000000843 powder Substances 0.000 claims abstract description 57
- 239000000463 material Substances 0.000 claims abstract description 45
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims abstract description 37
- 229930006000 Sucrose Natural products 0.000 claims abstract description 37
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims abstract description 36
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 34
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000005720 sucrose Substances 0.000 claims abstract description 32
- 239000008187 granular material Substances 0.000 claims abstract description 25
- 235000019359 magnesium stearate Nutrition 0.000 claims abstract description 18
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 17
- 238000002156 mixing Methods 0.000 claims abstract description 16
- 238000002360 preparation method Methods 0.000 claims abstract description 13
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims description 22
- 239000006071 cream Substances 0.000 claims description 13
- 229910000831 Steel Inorganic materials 0.000 claims description 12
- 239000010959 steel Substances 0.000 claims description 12
- 238000012946 outsourcing Methods 0.000 claims description 5
- 229960004793 sucrose Drugs 0.000 claims 7
- 210000000582 semen Anatomy 0.000 claims 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims 1
- 229940126678 chinese medicines Drugs 0.000 claims 1
- 239000000796 flavoring agent Substances 0.000 claims 1
- 235000019634 flavors Nutrition 0.000 claims 1
- 238000003754 machining Methods 0.000 claims 1
- 238000010298 pulverizing process Methods 0.000 claims 1
- 239000013078 crystal Substances 0.000 abstract description 9
- 238000004519 manufacturing process Methods 0.000 abstract description 8
- 238000000034 method Methods 0.000 abstract description 4
- 238000003860 storage Methods 0.000 abstract description 2
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 238000001514 detection method Methods 0.000 abstract 1
- 239000002994 raw material Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 238000000605 extraction Methods 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 238000005469 granulation Methods 0.000 description 8
- 230000003179 granulation Effects 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 239000007888 film coating Substances 0.000 description 7
- 238000009501 film coating Methods 0.000 description 7
- 239000003814 drug Substances 0.000 description 6
- 208000000059 Dyspnea Diseases 0.000 description 3
- 206010013975 Dyspnoeas Diseases 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 208000013220 shortness of breath Diseases 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 241000218671 Ephedra Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 235000008753 Papaver somniferum Nutrition 0.000 description 2
- 240000001090 Papaver somniferum Species 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 206010062717 Increased upper airway secretion Diseases 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 208000026435 phlegm Diseases 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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Abstract
Description
【技术领域】 【Technical field】
本发明涉及一种中药制剂及其制备方法,特别是一种用于治疗咳嗽、喘急气短的克咳片及其制备方法。 The invention relates to a traditional Chinese medicine preparation and a preparation method thereof, in particular to a Keke tablet for treating cough and shortness of breath and a preparation method thereof. the
【背景技术】 【Background technique】
克咳片是一个具有止嗽,定喘,祛痰功能的中成药,用于咳嗽,喘急气短的治疗,该产品处方由麻黄、罂粟壳、甘草、苦杏仁、桔梗、莱菔子、石膏七味中药组成。现有的克咳片制备方法为取麻黄和罂粟壳粉碎成细粉,过筛,留取45.8%细粉备用;剩余粗粉加酸性水溶液(用10%盐酸溶液调PH至5左右)煎煮二次,第一次加水10倍,第二次加水8倍,每次2小时,过滤,滤液用10%氢氧化钠溶液调PH值至7,药液备用;其余甘草等五味加水煎煮二次,第一次加水10倍,第二次加水8倍,每次1小时,过滤,滤液与上述溶液合并,浓缩至相对密度为1.20~1.25(60℃测)的稠膏,加入麻黄、罂粟壳细粉,混合均匀,在60~70℃干燥,粉碎成粗粉,过40目筛,得药材提取干膏粉;然后加入糖粉和硬脂酸镁适量,混匀,压制成1000片,包薄膜衣,即得。该药品由于疗效好,服用方便,已广泛地应用于咳嗽、喘急气短的治疗,但采用上述方法制备克咳片,由于压片前药粉含生药材的细粉量大,生药材细粉在每片克咳片中所占比例为61.1%,采用上述制备方法用压片机压片后所得的素片(素片即未包 薄膜衣前的药片)极易出现硬度差,容易裂片、松解、无法包薄膜衣或包薄膜衣后出现表面粗糙等现象,以致现有的克咳片在有效期内常出现裂片、稳定性差、检测不合格等问题,难以被生产厂家及广大消费者所接受。 Keke Tablets is a Chinese patent medicine with the functions of relieving cough, relieving asthma and eliminating phlegm. It is used for the treatment of cough and shortness of breath. Composition of traditional Chinese medicine. The existing Keke tablet preparation method is to take ephedra and poppy shells and crush them into fine powder, sieve, and keep 45.8% fine powder for later use; add acidic aqueous solution (use 10% hydrochloric acid solution to adjust the pH to about 5) and decoct the remaining coarse powder Second time, add water 10 times for the first time, add water 8 times for the second time, 2 hours each time, filter, adjust the pH value of the filtrate to 7 with 10% sodium hydroxide solution, and prepare the liquid medicine for later use; For the first time, add 10 times of water for the first time, add 8 times of water for the second time, each time for 1 hour, filter, combine the filtrate with the above solution, concentrate to a thick paste with a relative density of 1.20-1.25 (measured at 60°C), add ephedra and poppy Shell fine powder, mixed evenly, dried at 60-70°C, crushed into coarse powder, passed through a 40-mesh sieve, to obtain dry cream powder extracted from medicinal materials; then add appropriate amount of powdered sugar and magnesium stearate, mix well, and press into 1000 tablets, Film-coated, that is. The drug has been widely used in the treatment of cough and shortness of breath due to its good curative effect and convenient administration. The proportion in every Keke Tablet is 61.1%. The obtained plain tablet (the plain tablet is the tablet before the film coating) is very prone to poor hardness, easy to split, loose Problems such as unresolved, unable to be film-coated or surface rough after film-coating, so that the existing Keke tablets often have problems such as splits, poor stability, and unqualified testing within the validity period, which are difficult to be accepted by manufacturers and consumers . the
【发明内容】 【Content of invention】
本发明的目的在于针对上述存在的问题,提供一种可有效提高克咳片硬度和稳定性,防止其裂片、松片,并使所制得的素片符合包薄膜衣要求的克咳片及其制备方法。 The purpose of the present invention is to address the above existing problems, to provide a Keke tablet that can effectively improve the hardness and stability of the Keke tablet, prevent its splits and loose tablets, and make the prepared plain tablet meet the requirements of the film coating and the Keke tablet. its preparation method. the
本发明的技术方案如下: Technical scheme of the present invention is as follows:
本发明所述的克咳片,其组分包括药材提取干膏粉、蔗糖粉、药用滑石粉、药用二氧化硅、药用硬脂酸镁,其特点是还包括浓度为20-95%的药用酒精; The Keke Tablets of the present invention, its components include medicinal material extraction dry paste powder, sucrose powder, medicinal talcum powder, medicinal silicon dioxide, medicinal magnesium stearate, and is characterized in that it also includes a concentration of 20-95 % medicinal alcohol;
其中,每制备1000片上述克咳片上述各组分的重量配比为: Wherein, the weight ratio of the above-mentioned components for every 1000 above-mentioned Keke tablets prepared is:
药材提取干膏粉192~498g 蔗糖粉9.5~315.8g Medicinal extract dry paste powder 192~498g Sucrose powder 9.5~315.8g
药用滑石粉13.3~18g 药用二氧化硅13.3~18g Medicinal talcum powder 13.3~18g Medicinal silica 13.3~18g
药用硬脂酸镁0.89~1.21g 20-95%药用酒精4.7~156.6g; Medicinal magnesium stearate 0.89~1.21g 20-95% medicinal alcohol 4.7~156.6g;
上述各组分的重量配比最佳值为: The optimum weight ratio of each of the above components is:
药材提取干膏粉437g 蔗糖粉70.2g Medicinal extract dry cream powder 437g Sucrose powder 70.2g
药用滑石粉15.7g 药用二氧化硅15.7g Medicinal talcum powder 15.7g Medicinal silica 15.7g
药用硬脂酸镁1.05g 70%药用酒精34.8g; Medicinal magnesium stearate 1.05g 70% medicinal alcohol 34.8g;
本发明所述的克咳片的制备方法包括以下步骤: The preparation method of Keke tablet of the present invention comprises the following steps:
(1)、将一定重量的蔗糖粉置高效混合制粒机内,加入一定重 量的20-95%药用酒精,开动机器混合均匀。 (1), put a certain weight of sucrose powder in the high-efficiency mixing granulator, add a certain weight of 20-95% medicinal alcohol, and start the machine to mix evenly. the
(2)、将一定重量的药材提取干膏粉加入到上述高效混合制粒机内与蔗糖、20-95%药用酒精的混合物进行混合,同时开动机器及制粒切刀进行制粒(制粒即制成粒状),使全部物料形成以含20-95%药用酒精的蔗糖为晶核外包药材提取干膏粉的小颗粒。 (2), add a certain weight of medicinal material extraction dry paste powder into the above-mentioned high-efficiency mixing granulator and mix with the mixture of sucrose and 20-95% medicinal alcohol, and simultaneously start the machine and the granulation cutter for granulation ( granules (i.e. made into granules), so that all the materials form small granules that use sucrose containing 20-95% medicinal alcohol as the crystal nucleus to extract dry cream powder from outsourcing medicinal materials. the
(3)、将上述经过制粒的物料取出,通过摇摆式颗粒机过18目钢筛网。 (3), the above-mentioned granulated material is taken out, and passed through a 18-mesh steel screen by a swinging granulator. the
(4)、将上述通过18目钢筛网的物料移至三维混合机内,将一定重量的药用滑石粉、药用二氧化硅、药用硬脂酸镁加入三维混合机内与上述物料混合均匀,用压片机压片即得克咳片素片。 (4), the above-mentioned material passing through the 18-mesh steel screen is moved into the three-dimensional mixer, and a certain weight of medicinal talcum powder, medicinal silicon dioxide, and medicinal magnesium stearate are added to the three-dimensional mixer with the above-mentioned materials Mix evenly, and press into tablets with a tablet machine to obtain Keke Tablets Tablets. the
其中,上述步骤(1)中所用蔗糖粉投料前需粉碎过100目筛。 Wherein, the sucrose powder used in the above step (1) needs to be pulverized and passed through a 100-mesh sieve before feeding. the
本发明由于采用将一定重量的蔗糖粉置高效混合制粒机内加入一定重量的20-95%药用酒精先行混合均匀,使蔗糖粉呈现湿润状态并带有由20-95%酒精带入的少量水份,当将药材提取干膏粉加入高效混合制粒机开动机器混合并打开制粒切刀时,可形成无数以湿润的蔗糖颗粒为晶核,外包药材提取干膏粉的小颗粒,由于颗粒内部的蔗糖晶核含有少量水份,故此种颗粒呈现外干内湿的状态,当颗粒进入压片机模具内进行压片时,颗粒在模具内受到压片机上冲头、下冲头压力的作用,颗粒内的蔗糖晶核释放出少量的水份,导致颗粒外层的干膏粉被水份润湿,从而引发药材提取干膏粉的黏性,使受压后的颗粒与颗粒之间通过此黏性以及颗粒之间释放的水份所形成的水桥(水桥即颗粒与颗粒之间释放的水份连接在一起形成的类似于桥状的结 构,包括某些物质通过水发生的键结合作用)紧密黏结起来,使压片所得的素片硬度高,表面光洁细腻,不易裂片、松片,并完全符合包薄膜衣的要求,从而有效地提高了克咳片的稳定性,大大地减少了该制剂在生产、运输、储藏过程因素片硬度不足、裂片、松片、表面粗糙所导致的无法包薄膜衣、稳定性差、检测不合格等现象的发生,确保了本发明的克咳片在生产时的可操作性以及产品在有效期内的性能稳定性,而且其制备工艺简单、易行、生产成本低。 In the present invention, because a certain weight of sucrose powder is placed in a high-efficiency mixing granulator, a certain weight of 20-95% medicinal alcohol is added and mixed evenly, so that the sucrose powder is in a wet state and contains the 20-95% alcohol. A small amount of water, when adding the dry paste powder of medicinal material extraction to the high-efficiency mixing granulator to start the machine to mix and open the granulation cutter, countless small particles of the dry paste powder of the outsourced medicinal material extraction can be formed with moist sucrose particles as crystal nuclei. Because the sucrose crystal nuclei inside the granules contain a small amount of water, the granules are dry on the outside and wet on the inside. When the granules enter the mold of the tablet machine for tableting, the granules are pressed by the upper punch and the lower punch of the tablet machine in the mold. Under the action of pressure, the sucrose crystal nuclei in the granules release a small amount of water, which causes the dry paste powder on the outer layer of the granules to be wetted by water, thereby causing the viscosity of the dry paste powder extracted from medicinal materials, making the compressed granules and granules The water bridge formed by this viscosity and the water released between the particles (the water bridge is a bridge-like structure formed by the water released between the particles and the particles, including certain substances passing through Bonding effect of water) tightly bonded together, so that the plain tablets obtained by tableting have high hardness, smooth and delicate surface, not easy to split and loose, and fully meet the requirements of film coating, thus effectively improving the stability of Keke Tablets It greatly reduces the occurrence of phenomena such as incapability of film coating, poor stability, and unqualified testing caused by factors such as insufficient tablet hardness, splits, loose tablets, and rough surfaces during production, transportation, and storage of the preparation, ensuring that the present invention The operability of the Keke Tablet during production and the performance stability of the product within the valid period, and its preparation process is simple, easy to implement and low in production cost. the
【具体实施方式】 【Detailed ways】
下面结合具体实施方式对本发明作进一步详细描述: Below in conjunction with specific embodiment the present invention is described in further detail:
本发明所述的克咳片,其组分包括药材提取干膏粉、蔗糖粉、药用滑石粉、药用二氧化硅、药用硬脂酸镁、药用酒精。 The Keke Tablets of the present invention, its components include medicinal material extraction dry cream powder, sucrose powder, medicinal talcum powder, medicinal silicon dioxide, medicinal magnesium stearate, and medicinal alcohol. the
药用酒精的浓度为20-95%,即药用酒精中酒精的体积百分数为20-95%。 The concentration of medicinal alcohol is 20-95%, that is, the volume percentage of alcohol in medicinal alcohol is 20-95%. the
其中,每1000片上述克咳片中各组分的重量配比为: Wherein, the weight ratio of each component in every 1000 above-mentioned Keke Tablets is:
药材提取干膏粉 192~498g 蔗糖粉9.5~315.8g Medicinal extract dry cream powder 192~498g Sucrose powder 9.5~315.8g
药用滑石粉 13.3~18g 药用二氧化硅13.3~18g Medicinal talcum powder 13.3~18g Medicinal silicon dioxide 13.3~18g
药用硬脂酸镁0.89~1.21g 20-95%药用酒精4.7~156.6g Medicinal magnesium stearate 0.89~1.21g 20-95% medicinal alcohol 4.7~156.6g
上述各组分的重量配比最佳值为: The optimum weight ratio of each of the above components is:
药材提取干膏粉437g 蔗糖粉70.2g Medicinal extract dry cream powder 437g Sucrose powder 70.2g
药用滑石粉15.7g 药用二氧化硅15.7g Medicinal talcum powder 15.7g Medicinal silicon dioxide 15.7g
药用硬脂酸镁1.05g 70%药用酒精34.8g Medicinal magnesium stearate 1.05g 70% medicinal alcohol 34.8g
本发明所述的克咳片的制备方法包括以下步骤: The preparation method of Keke tablet of the present invention comprises the following steps:
(1)、将一定重量的蔗糖粉置高效混合制粒机内,加入一定重量的20-95%药用酒精,开动机器混合均匀。 (1), put a certain weight of sucrose powder in the high-efficiency mixing granulator, add a certain weight of 20-95% medicinal alcohol, and start the machine to mix evenly. the
(2)、将一定重量的药材提取干膏粉加入到上述高效混合制粒机内与蔗糖、20-95%药用酒精的混合物进行混合,同时开动机器及制粒切刀进行制粒(制粒即制成粒状),使全部物料形成无数以含20-95%药用酒精的蔗糖为晶核外包药材提取干膏粉的小颗粒。 (2), add a certain weight of medicinal material extraction dry paste powder into the above-mentioned high-efficiency mixing granulator and mix with the mixture of sucrose and 20-95% medicinal alcohol, and simultaneously start the machine and the granulation cutter for granulation ( (i.e., granules are made into granules), so that all the materials form numerous small granules that use sucrose containing 20-95% medicinal alcohol as the crystal nucleus to extract dry cream powder from outsourcing medicinal materials. the
(3)、将上述经过制粒的物料取出,通过摇摆式颗粒机过18目钢筛网。 (3), the above-mentioned granulated material is taken out, and passed through a 18-mesh steel screen by a swinging granulator. the
(4)、将上述通过18目钢筛网的物料移至三维混合机内,将一定重量的药用滑石粉、药用二氧化硅、药用硬脂酸镁加入三维混合机内与上述物料混合均匀,用压片机压片即得克咳片素片。 (4), the above-mentioned material passing through the 18-mesh steel screen is moved into the three-dimensional mixer, and a certain weight of medicinal talcum powder, medicinal silicon dioxide, and medicinal magnesium stearate are added to the three-dimensional mixer with the above-mentioned materials Mix evenly, and press into tablets with a tablet machine to obtain Keke Tablets Tablets. the
其中,上述步骤(1)中所用蔗糖粉投料前需粉碎过100目筛。 Wherein, the sucrose powder used in the above step (1) needs to be pulverized and passed through a 100-mesh sieve before feeding. the
实施例1:先将315.8g蔗糖粉置高效混合制粒机内,加入156.6g的95%药用酒精,开动机器混合均匀;将192g的药材提取干膏粉加入到上述高效混合制粒机内与蔗糖、95%药用酒精的混合物进行混合,同时开动机器及制粒切刀进行制粒(即制成粒状),使全部物料形成以含95%药用酒精的蔗糖为晶核外包药材提取干膏粉的小颗粒;将上述经过制粒的物料取出,通过摇摆式颗粒机过18目钢筛网;将上述通过18目钢筛网的物料移至三维混合机内,将15.7g的药用滑石粉、15.7g的药用二氧化硅、1.05g的药用硬脂酸镁加入三维混合机内与上述物料混合均匀,用压片机压片即得1000片克咳片素片。 Example 1: First put 315.8g of sucrose powder in the high-efficiency mixing granulator, add 156.6g of 95% medicinal alcohol, start the machine and mix evenly; add 192g of medicinal material extraction dry paste powder into the above-mentioned high-efficiency mixing granulator Mix with a mixture of sucrose and 95% medicinal alcohol, and at the same time start the machine and granulation cutter to granulate (i.e. make granules), so that all materials are formed and the sucrose containing 95% medicinal alcohol is used as the crystal nucleus to extract medicinal materials outsourced Small particles of dry paste powder; take out the above-mentioned granulated material, and pass through a 18-mesh steel screen through a swing granulator; move the above-mentioned material that has passed through the 18-mesh steel screen into a three-dimensional mixer, and mix 15.7g of the medicine Add talcum powder, 15.7g of medicinal silicon dioxide, and 1.05g of medicinal magnesium stearate into a three-dimensional mixer and mix with the above-mentioned materials evenly, and press into tablets with a tablet machine to obtain 1000 grams of cough tablets. the
实施例2:先将70.2g蔗糖粉置高效混合制粒机内,加入34.8g 的70%药用酒精,开动机器混合均匀;将437g的药材提取干膏粉加入到上述高效混合制粒机内与蔗糖、70%药用酒精的混合物进行混合,同时开动机器及制粒切刀进行制粒,使全部物料形成以含70%药用酒精的蔗糖为晶核外包药材提取干膏粉的小颗粒;将上述经过制粒的物料取出,通过摇摆式颗粒机过18目钢筛网;将上述通过18目钢筛网的物料移至三维混合机内,将15.7g的药用滑石粉、15.7g的药用二氧化硅、1.05g的药用硬脂酸镁加入三维混合机内与上述物料混合均匀,用压片机压片即得1000片克咳片素片。 Example 2: First put 70.2g of sucrose powder in the high-efficiency mixing granulator, add 34.8g of 70% medicinal alcohol, start the machine and mix evenly; add 437g of medicinal material extraction dry paste powder into the above-mentioned high-efficiency mixing granulator Mix with a mixture of sucrose and 70% medicinal alcohol, and at the same time start the machine and granulating cutter to granulate, so that all materials form small particles of dry cream powder extracted from outsourcing medicinal materials with 70% medicinal alcohol as the crystal nucleus The above-mentioned material through granulation is taken out, and crosses 18 mesh steel screens by a swinging granulator; the above-mentioned material passing through 18 mesh steel screens is moved to a three-dimensional mixer, and 15.7g of medicinal talcum powder, 15.7g The medicinal silica of 1.05g and the medicinal magnesium stearate of 1.05g are added in the three-dimensional mixer and mixed evenly with the above-mentioned materials, and are pressed into tablets with a tablet machine to obtain 1000 grams of cough tablets. the
实施例3:先将9.5g蔗糖粉置高效混合制粒机内,加入4.7g的25%药用酒精,开动机器混合均匀;将498g的药材提取干膏粉加入到上述高效混合制粒机内与蔗糖、25%药用酒精的混合物进行混合,同时开动机器及制粒切刀进行制粒,使全部物料形成以含25%药用酒精的蔗糖为晶核外包药材提取干膏粉的小颗粒;将上述经过制粒的物料取出,通过摇摆式颗粒机过18目钢筛网;将上述通过18目钢筛网的物料移至三维混合机内,将15.7g的药用滑石粉、15.7g的药用二氧化硅、1.05g的药用硬脂酸镁加入三维混合机内与上述物料混合均匀,用压片机压片即得1000片克咳片素片。 Example 3: first put 9.5g of sucrose powder in the high-efficiency mixing granulator, add 4.7g of 25% medicinal alcohol, start the machine and mix evenly; add 498g of medicinal material extraction dry paste powder into the above-mentioned high-efficiency mixing granulator Mix with a mixture of sucrose and 25% medicinal alcohol, and at the same time start the machine and granulating cutter to granulate, so that all the materials form small particles of dry paste powder extracted from outsourcing medicinal materials with 25% medicinal alcohol as the crystal nucleus. The above-mentioned material through granulation is taken out, and crosses 18 mesh steel screens by a swinging granulator; the above-mentioned material passing through 18 mesh steel screens is moved to a three-dimensional mixer, and 15.7g of medicinal talcum powder, 15.7g The medicinal silica of 1.05g and the medicinal magnesium stearate of 1.05g are added in the three-dimensional mixer and mixed evenly with the above-mentioned materials, and are pressed into tablets with a tablet machine to obtain 1000 grams of cough tablets. the
为表明本发明所述克咳片所具备的硬度以及稳定性,将上述实施例1、实施例2、实施例3所制备的克咳片素片分别与采用现有技术生产的克咳片进行硬度测试,脆碎度测试,包薄膜衣试验,恒温加速试验,破坏性试验,结果显示本发明的克咳片与现有的克咳片相比表现出较高的硬度和相当的稳定性,包薄膜衣后的效果非常理想,表面 光滑细腻、美观。 In order to demonstrate the hardness and stability of the Keke Tablets of the present invention, the Keke Tablets prepared in Example 1, Example 2, and Example 3 were respectively compared with the Keke Tablets produced by the prior art. Hardness test, friability test, film coating test, constant temperature acceleration test, destructive test, the results show that compared with the existing Keke Tablets, Keke Tablets of the present invention exhibit higher hardness and considerable stability, The effect after film coating is very ideal, the surface is smooth, delicate and beautiful. the
其中,硬度测试的结果如下:现有技术的工艺生产硬度:<5Kgf;采用本发明的工艺生产硬度:>12Kgf(Kgf即千克力,相当于一千克的物体所受到重力的一个这么大的力,也就是9.8N的力);脆碎度测试的结果如下:现有技术的工艺生产脆碎度:>3%;采用本发明的工艺生产脆碎度:<0.3%。 Wherein, the result of hardness test is as follows: the technology production hardness of prior art:<5Kgf; Adopt the technology production hardness of the present invention:>12Kgf (Kgf is the kilogram force, is equivalent to such a large force of the suffered gravity of a kilogram , that is, a force of 9.8N); the results of the friability test are as follows: the friability produced by the process of the prior art: > 3%; the friability produced by the process of the present invention: <0.3%. the
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吕晓英等.克服中药片剂松片的方法探讨.《基层中药杂志》.1997,第11卷(第2期),24-25页. * |
张国安.影响中药片剂硬度的因素及解决方法.《时珍国医国药》.2003,第14卷(第7期),430-431页. * |
谢秀琼等.现代中药制剂新技术.《现代中药制剂新技术》.2004,251-257页. * |
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