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Preparation method of crystalline clopidogrel bisulfate tablets

A technology of clopidogrel bisulfate tablets and clopidogrel bisulfate, which is applied to medical preparations containing no active ingredients, medical preparations containing active ingredients, pill delivery, etc. If it is not processed, there are still problems such as sticking and punching when pressing tablets

Active Publication Date: 2013-04-10
天津泰普制药有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In order to ensure that its related substances will not increase, therefore: the conventional wet granulation tabletting method cannot be used; if the raw material and auxiliary materials are used for direct tableting, it is not feasible to stick the raw material and have cracks; if the dry granulation tabletting method is used, the raw material granules The surface treatment is not complete, and it is better than direct tableting during tableting. There is also the possibility of sticking and splitting, and it increases the processing process, which is not suitable for large-scale production; if hot-melt granulation is used, the main drug is added with other excipients and then mixed with polyethylene Diol 6000 is mixed and heated, and related substances increase; and the main drug and polyethylene glycol 6000 do not infiltrate, the surface of the main drug cannot be treated, and the tablet is still sticky.

Method used

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  • Preparation method of crystalline clopidogrel bisulfate tablets
  • Preparation method of crystalline clopidogrel bisulfate tablets

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0054] Type I clopidogrel hydrogen sulfate 98.875g

[0055] Methanol 300ml

[0056] Polyethylene glycol 4000 10g

[0057] Hydroxypropyl cellulose 2g

[0058] Lactose 118g

[0059] Microcrystalline cellulose 19g

[0060] Pregelatinized starch 8.125g

[0061] Hydrogenated vegetable oil 3g

[0062] Process: Sieving type I clopidogrel hydrogen sulfate according to the above weight for later use; take polyethylene glycol and hydroxypropyl cellulose in methanol and stir to dissolve and let cool, add type I clopidogrel hydrogen sulfate; evaporate the solvent, Leave to cool to room temperature; sieve to obtain clopidogrel hydrogen sulfate clathrate granules and other auxiliary materials, mix and tablet.

Embodiment 2

[0064] Clopidogrel hydrogen sulfate 97.875g

[0065] Acetone 50ml

[0066] Polyethylene glycol 6000 5g

[0067] Lactose 118g

[0068] Microcrystalline cellulose 19g

[0069] Pregelatinized starch 8.125g

[0070] Hydrogenated vegetable oil 3g

[0071] Process: Sieving clopidogrel bisulfate according to the above weight for use; stir the polyethylene glycol in acetone and dissolve it by heating, then let it cool, add clopidogrel bisulfate, evaporate the solvent, and sieve to obtain clopidogrel bisulfate The inclusion agent granules are then mixed with other excipients and compressed into tablets.

Embodiment 3

[0073] Clopidogrel hydrogen sulfate 97.875g

[0074] Chloroform 250ml

[0075] Polyethylene glycol 10000 10g

[0076] Lactose 118g

[0077] Microcrystalline cellulose 19g

[0078] Pregelatinized starch 8.125g

[0079] Hydrogenated vegetable oil 3g

[0080] Process: Sieving clopidogrel bisulfate according to the above weight for use; take polyethylene glycol in chloroform, stir and heat to dissolve and then let it cool, add clopidogrel bisulfate, stir and heat to 45°C to dissolve the evaporated solvent, and sieve to obtain Clopidogrel bisulfate clathrate granules are then mixed with other excipients and compressed into tablets.

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Abstract

The invention provides a preparation method of crystalline clopidogrel bisulfate tablets, comprising the following steps of: mixing a medicinal solvent and an inclusion agent with stirring, dissolving by heating to the temperature of 35-90 DEG C, staying cool to room temperature; adding the crystalline clopidogrel bisulfate with uniformly stirring; drying the medicinal solvent by distillation, sieving to obtain clopidogrel bisulfate inclusion particles; uniformly mixing the obtained clopidogrel bisulfate inclusion particles and a pharmaceutic adjuvant at the weight part ratio of 1:0.02-10, followed by tabletting, wherein the addition amount of the inclusion agent is 0.05-0.2 times the weight of clopidogrel bisulfate and the addition amount of the medicinal solvent is 0.5-10 times the weight of clopidogrel bisulfate. According to the clopidogrel bisulfate tablets provided by the invention, the crystal form is not changed; related substances are not increased, the fluidity and compressibility of the raw materials are enhanced, and the stability of the tablets is raised; in addition, the preparation method of the tablets is more suitable for large-scale industrial production.

Description

Technical field [0001] The invention belongs to the technical field of pharmaceutical preparations, and relates to a preparation method of crystalline clopidogrel hydrogen sulfate tablets. Background technique [0002] Cardiovascular and cerebrovascular thrombotic diseases are a common disease in my country and an important cause of death. Especially in recent years, the incidence of thromboembolic diseases, mainly coronary thrombosis and cerebral thrombosis, has been on the rise, seriously endangering human health. [0003] Clopidogrel is a platelet aggregation inhibitor. The ATC classification is: B01AC / 04. Clopidogrel also selectively inhibits the binding of adenosine diphosphate (ADP) to its platelet receptor and the secondary activation of the ADP-mediated glycoprotein GP111b / llla complex, so it can inhibit platelet aggregation. Clopidogrel must Only through biotransformation can platelet aggregation be inhibited, but the active metabolites that produce this effect have not...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/20A61K31/4365A61K47/34A61K47/38A61K47/36A61K47/44A61P9/10A61P9/00A61P7/02
Inventor 周世旺刘衡姜瑛
Owner 天津泰普制药有限公司
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