Aspirin sustained-release tablets and preparation method thereof

A technology of aspirin and sustained-release tablets, which is applied in the direction of pharmaceutical formulas, medical preparations with non-active ingredients, medical preparations containing active ingredients, etc., can solve problems such as poor quality stability, large quality differences, stimulation, etc., and achieve uniform quality Good sex, good stability, safe drug effect

Inactive Publication Date: 2020-09-25
郑州市协和制药厂
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] The patent number is CN201310099684.0, and the patent name is an aspirin sustained-release tablet and its preparation method. It is the applicant's prior patent. From this prior patent, it can be concluded that it is used to prepare aspirin sustained-release tablets Tablets and their preparation method, the problems solved by the previous patents are unstable release rate, large quality differences between different batches of tablets and different tablets in the same batch, but because of the selection of auxiliary materials and long drying time, etc., In the following quality stability inspection, we found that the product produced by this method will have a faster release rate and an increase in the content

Method used

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  • Aspirin sustained-release tablets and preparation method thereof
  • Aspirin sustained-release tablets and preparation method thereof
  • Aspirin sustained-release tablets and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0017] Take 750 parts of aspirin (the corresponding weight is 75.0g, and the rest of the ingredients follow this ratio), 35 parts of starch, 63 parts of polyacrylic acid resin II, 54 parts of hypromellose, and 8 parts of ethyl cellulose, and grind them through an 80-mesh sieve net, spare.

[0018] 3% hypromellose alcohol solution prescription, including tartaric acid, water, polysorbate 80, hypromellose, 95% ethanol.

[0019] Prepare 3% hypromellose alcohol solution: add 135 parts of tartaric acid to 360 parts of purified water, heat to about 70°C and stir to completely dissolve, then add 36 parts of polysorbate 80, stir to completely dissolve, and obtain solution A; Another 54 parts of hypromellose was added while stirring, and it was evenly dispersed in 1152 parts of ethanol to obtain solution B; the obtained two solutions of A and B were mixed evenly, and placed at 18°C ​​for 8 hours.

[0020] The above tartaric acid, water, polysorbate 80, hypromellose, ethyl cellulose, and

Embodiment 2

[0029] Take 750 parts of aspirin, 30 parts of starch, 50 parts of polyacrylic resin II, 40 parts of hypromellose, and 8 parts of ethyl cellulose, grind them through an 80-mesh sieve, and set aside.

[0030] 3% hypromellose alcohol solution prescription, including tartaric acid, water, polysorbate 80, hypromellose, 95% ethanol.

[0031] Prepare 3% hypromellose alcohol solution: add 100 parts of tartaric acid to 200 parts of purified water, heat to about 70°C and stir to completely dissolve, then add 20 parts of polysorbate 80, stir to completely dissolve, and obtain solution A; Another 54 parts of hypromellose was added while stirring, and it was evenly dispersed in 600 parts of ethanol to obtain solution B; the obtained two solutions of A and B were mixed evenly, and placed at 20°C for 30 hours.

[0032] The above tartaric acid, water, polysorbate 80, hypromellose, ethyl cellulose, and 95% ethanol all should meet the requirements of "The Pharmacopoeia of the People's Republic of

Embodiment 3

[0041] Take 750 parts of aspirin, 50 parts of starch, 70 parts of polyacrylic resin II, 60 parts of hypromellose, and 8 parts of ethyl cellulose, grind them through an 80-mesh sieve, and set aside.

[0042] 3% hypromellose alcohol solution prescription, including tartaric acid, water, polysorbate 80, hypromellose, 95% ethanol.

[0043]Prepare 3% hypromellose alcohol solution: add 150 parts of tartaric acid to 500 parts of purified water, heat to about 70°C and stir to completely dissolve, then add 50 parts of polysorbate 80, stir to completely dissolve, and obtain solution A; Another 60 parts of hypromellose was added while stirring, and it was evenly dispersed in 1500 parts of ethanol to obtain solution B; the obtained two solutions of A and B were mixed evenly, and placed at 26°C for 72 hours.

[0044] The above tartaric acid, water, polysorbate 80, hypromellose, ethyl cellulose, and 95% ethanol all should meet the requirements of "The Pharmacopoeia of the People's Republic of

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Abstract

The invention relates to aspirin sustained-release tablets and a preparation method thereof. The sustained-release tablets include main drug-aspirin and ingredients; the ingredients include starch, polyacrylic resin II, hydroxypropyl methylcellulose, ethyl cellulose and a 3% hydroxypropyl methylcellulose alcoholic solution; and the starch, the polyacrylic resin II, the hydroxypropyl methylcellulose and the ethyl cellulose in the ingredients are smashed and sieved through a sieve with 80 meshes for later use. The preparation method of the 3% hydroxypropyl methylcellulose alcoholic solution in the ingredients includes taking 135 parts of tartaric acid to add to 360 parts of purified water, performing heating to about 70 DEG C to stir to complete dissolution, then adding 36 parts of polysorbate 80, and performing stirring to complete dissolution so as to obtain a solution A; taking 54 parts of the hydroxypropyl methylcellulose, while adding, performing stirring to uniformly dispersing thehydroxypropyl methylcellulose in 1152 parts of ethanol, and obtaining a solution B; and uniformly mixing the solutions A and B, and performing standing for 8-72 h at 18-26 DEG C. The sustained-release tablets have the advantages of being sustainably stable in release rate, free from pollution and almost insoluble in stomach.

Description

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Claims

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Application Information

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Owner 郑州市协和制药厂
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