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Slow-releasing tablets of oral medicine and preparation thereof

A technology for sustained-release tablets and oral medicines, which is applied in the field of oral drug sustained-release tablets and its preparation, which can solve problems such as inability to achieve a good sustained-release effect, achieve enhanced blocking effects, ensure sustained-release effects, and reduce The effect of release area

Inactive Publication Date: 2007-08-08
南京亿华药业有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This sustained-release tablet often cannot achieve a good sustained-release effect for the main drug with good water solubility.

Method used

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  • Slow-releasing tablets of oral medicine and preparation thereof
  • Slow-releasing tablets of oral medicine and preparation thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] First, put the raw materials and auxiliary materials at 60°C and dry them for 4 hours, pass through a 80-mesh sieve, and set aside; then, prepare a drug-free blank layer: take 200 g of glyceryl behenate, polyvinylpyrrolidone (PVP) K30 15g was mixed uniformly by the method of increasing in equal amounts, passed through a 60-mesh sieve, and dry-granulated; the second drug-containing slow-release layer of the preparation layer: metformin hydrochloride 500g, glyceryl behenate 150g, polyvinylpyrrolidone (PVP) K30 20g were increased in equal amounts Mix evenly by 60-mesh sieve, dry granulate, and weigh; Tablet: layer 1 and layer 2 are mixed with 1% magnesium stearate respectively, and the particles of layer 1 and layer 2 are separated into two hoppers in a double-layer Compressed into 1000 tablets on a tablet press, each containing 500 mg of metformin hydrochloride. The blood concentration-time curve after taking the medicine is shown in Figure 2.

Embodiment 2

[0039] First, put the raw materials and auxiliary materials at 60°C for 4 hours, pass through an 80-mesh sieve for later use; then, prepare a blank layer without drugs: take 275g of high-viscosity hydroxypropyl methylcellulose, polyvinylpyrrolidone (PVP) K30 15g was uniformly mixed according to equal increment method, passed through a 60-mesh sieve, dry-granulated, and weighed; preparation layer 2 slow-release layer: get metformin hydrochloride 500g, hydroxypropyl methylcellulose 150g, polyvinylpyrrolidone ( PVP) K30 15g is mixed evenly by the method of equal increment, passed through a 60-mesh sieve, dry granulated, and weighed; tableting: layer 1 and layer 2 are mixed with 1% micropowder silica gel respectively, and the particles of layer 1 and layer 2 are separated Two hoppers are pressed into 1000 tablets on a double-layer tablet press, and each tablet contains 500 mg of metformin hydrochloride. The blood drug concentration-time curve after taking the medicine is similar t...

Embodiment 3

[0041] First, put the raw materials and auxiliary materials at 60°C for 4 hours, pass through an 80-mesh sieve for later use; then, prepare a blank layer without drugs: take 300 g of ethyl cellulose, 15 g of polyvinylpyrrolidone (PVP) K30 and press Mix evenly by the equal-volume incremental method, pass through a 60-mesh sieve, use water as a binder, wet granulate, and weigh; prepare the second sustained-release layer: take 500g of metformin hydrochloride, 200g of ethyl cellulose, and polyvinylpyrrolidone (PVP) K30 10g was mixed evenly by the method of equal increment, passed through a 60-mesh sieve, wet granulated, and weighed; tableting: layer 1 and layer 2 were mixed with 1% magnesium stearate respectively, and the granules of layer 1 and layer 2 were separated into two A hopper is compressed into 1000 tablets on a double-layer tablet press, and each tablet contains 500 mg of metformin hydrochloride. The blood drug concentration-time curve after taking medicine is similar t...

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Abstract

A slow-releasing tablet of orally taken medicine is composed of a blank layer consisting of slow-releasing material, adhesive and lubricant, and a slow-releasing layer prepared from water-soluble medicine, slow releasing material, adhesive and lubricant. Its advantage is durable and stable blood concentration.

Description

1. Technical field [0001] The invention relates to a slow-release tablet for oral administration and a preparation method thereof 2. Background technology [0002] Some drugs used clinically, due to the nature of some drugs, are made into ordinary tablets and taken, and will be quickly metabolized in the human body. In order to achieve an effective therapeutic effect, the frequency of taking such drugs must be increased. This will cause the shortcomings of many times of taking medicine, large fluctuations in blood drug concentration, and large side effects. In order to improve the curative effect of medicines, reduce the number of times of taking medicines, and ensure the safety of medicines, these medicines must be made into slow-release tablets. Sustained-release tablets are usually made of uniform sustained-release tablets by mixing the main drug, sustained-release materials, binders and lubricants uniformly and then compressing the tablets. Such sustained-release tabl...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/22A61K31/155A61K31/215A61K31/404A61P3/10A61P25/00A61P9/12
Inventor 杨鹏辉
Owner 南京亿华药业有限公司