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Lumbrokinase enteric-coated tablet and preparation method thereof

A lumbrokinase entero and lumbrokinase technology, which is applied in pharmaceutical formulations, medical preparations with non-active ingredients, and medical preparations containing active ingredients, etc., can solve the problems of low probability of capsules, increased pollution, and high product cost, and achieves The quality and curative effect are stable and reliable, the effect of overcoming the reduction of potency and overcoming technical defects

Active Publication Date: 2013-11-13
长春雷允上药业有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the quality of lumbrokinase enteric-coated capsules is unstable, and they tend to become brittle when stored, and the probability of capsules being used is very low.
The drug powder in the damaged capsule is easy to stick to the surface of other intact capsules. Although most of the drug powder can be removed by polishing, the drug powder at the interface is difficult to remove, which not only causes a lot of waste of drug powder, but also increases the chance of pollution and prolongs production. cycle
In addition, gastric acid may penetrate into the capsule through the interface, destroying the active ingredients and reducing the efficacy of the medicine.
The preparation process of lumbrokinase enteric-coated pellets is to freeze-dry the lumbrokinase concentrated solution to obtain lumbrokinase dry powder, and wrap the mixed powder of dry powder and starch on the blank pellet core through the action of adhesive. The drying process requires a lot of energy and the product cost is high
Relatively speaking, the preparation of lumbrokinase enteric-coated tablets can avoid these defects, but in the production of lumbrokinase enteric-coated tablets, the type and amount of excipients, drying time and temperature of granules will all affect the product quality
For example, Xu Jian (“Research on Lumbrokinase Enteric-Coated Tablets”, Xu Jian, Proceedings of the Fourth China New Medicine Doctor Forum, pp. 242-246) proposed a preparation process for lumbrokinase enteric-coated tablets, However, this preparation process causes fragmentation and capping of the tablets during the tableting process, and the disintegration time limit does not meet the requirements, so it cannot be applied to the industrial production of lumbrokinase enteric-coated tablets.

Method used

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  • Lumbrokinase enteric-coated tablet and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] The preparation of embodiment 1 lumbrokinase enteric-coated tablets

[0031] 1. Prescription (600,000 tablets):

[0032]

[0033] 2. Preparation process

[0034] 1. wet granules

[0035] All raw and auxiliary materials must reach 80-mesh fineness, sucrose is crushed with a universal grinder, and passed through a 80-mesh sieve. Prepare wet granules in four batches, each batch of raw and auxiliary materials is: 45 billion units of lumbrokinase raw material powder (about 2.5kg), 3.75kg of hydroxypropyl cellulose, 30.45kg of sucrose, 0.575kg of sodium carboxymethyl starch, Put 1.9kg of talcum powder in the mixer of the high-speed mixing granulator, turn on the stirring paddle (1500 rpm) and mix for 15 minutes; add 15kg of 50% (volume ratio) ethanol aqueous solution, turn on the stirring paddle (1500 rpm) and mix for 2 ~7 minutes, then turn on the stirring paddle (3000 rpm) and the granulating paddle (3000 rpm) to mix and granulate for 1-2 minutes; open the discharge v...

Embodiment 2

[0113] Preparation of embodiment 2 lumbrokinase enteric-coated tablets

[0114] 1. Prescription (600,000 tablets):

[0115]

[0116] 2. Preparation process

[0117] 1. wet granules

[0118] All raw and auxiliary materials must reach 80-mesh fineness, sucrose is crushed with a universal grinder, and passed through a 80-mesh sieve. Prepare wet granules in four batches, each batch of raw and auxiliary materials: Lumbrokinase raw material powder 45 billion units (about 2.5kg), hydroxypropyl cellulose 3.75kg, sucrose 30.45kg, sodium carboxymethyl starch 0.575kg, talc Put 1.9kg of powder into the mixer of the high-speed mixing granulator, turn on the stirring paddle (1500 rpm) and mix for 15 minutes; add 15kg of 50% (volume ratio) ethanol aqueous solution, turn on the stirring paddle (1500 rpm) and mix for 2~ After 7 minutes, turn on the stirring paddle (3000 rpm) and the granulating paddle (3000 rpm) to mix and granulate for 1 to 2 minutes; open the discharge valve and discha...

Embodiment 3

[0136] The preparation of embodiment 3 lumbrokinase enteric-coated tablets

[0137] 1. Prescription (600,000 tablets):

[0138]

[0139]

[0140] 2. Preparation process

[0141] 1. wet granules

[0142] All raw and auxiliary materials must reach 80-mesh fineness, sucrose is crushed with a universal grinder, and passed through a 80-mesh sieve. Prepare wet granules in four batches, each batch of raw and auxiliary materials: Lumbrokinase raw material powder 45 billion units (about 2.50kg), hydroxypropyl cellulose 3kg, sucrose 36.54kg, carboxymethyl starch sodium 0.575kg, talc powder 2.28kg, put it in the mixer of the high-speed mixing granulator, turn on the stirring paddle (1500 rpm) and mix for 15 minutes; add 15kg of ethanol (50%) aqueous solution, turn on the stirring paddle (1500 rpm) and mix for 2 to 7 minutes , and then turn on the stirring paddle (3000 rpm) and the granulating paddle (3000 rpm) to mix and granulate for 1 to 2 minutes; open the discharge valve and...

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Abstract

The invention provides a lumbrokinase enteric-coated tablet and a preparation method thereof. The lumbrokinase enteric-coated tablet comprises following components in parts by weight: 5 to 15 parts of lumbrokinase, 7.5 to 22.5 parts of hydroxy propyl cellulose, 3.8 to 11.4 parts of powdered steatile, 1.5 to 4.5 parts of magnesium stearate, 2.3 to 6.9 parts of carboxy methyl starch sodium, and 63.9 to 185.7 part of cane sugar, wherein the titer of the lumbrokinase is between 0.9 multiply 104 and 2.7 multiple 104 unit / milligram. Compared to the conventional lumbrokinase preparation and the preparation technology thereof, the lumbrokinase enteric-coated tablet and the preparation method thereof are improved, the quality and curative effect of the lumbrokinase enteric-coated tablet are more stable and reliable, each parameter of the product reaches or exceeds the national drug standards, furthermore, the lumbrokinase stability of the active components is prominently improved, the technical defect that the titer of the thermal sensitive components reduces during the preparation and storage processes is overcome, so that the curative effect of the lumbrokinase on corresponding diseases in clinic is largely improved.

Description

technical field [0001] The invention belongs to the field of pharmacy, and relates to an enteric-coated tablet and a preparation method thereof, in particular to a lumbrokinase enteric-coated tablet and a preparation method thereof. Background technique [0002] Lumbrokinase is a kind of proteolytic enzyme extracted and isolated from the artificially cultivated Eisenia chinensis. It has a selective affinity for fibrinogen, can directly hydrolyze fibrinogen, produce soluble fibrinogen degradation products, and reduce fibrin The original content, preventing thrombosis. Lumbrokinase contains plasminogen activator, plasmin and other components, which can degrade insoluble fibrin by promoting the conversion of plasminogen into plasmin, and can dissolve thrombus in early cerebral infarction. A large number of clinical studies have shown that lumbrokinase has a strong role in dissolving thrombus, inhibiting platelet aggregation, reducing fibrinogen and improving the hypercoagulabl...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K38/48A61K9/20A61K47/12A61K47/02A61K47/26A61P7/02A61P9/10A61P25/00A61P25/28A61P25/20
Inventor 邵春杰
Owner 长春雷允上药业有限公司
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