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Compound paracetamol and chlorphenamine maleate slow releasing tablet and its preparation

A technology for compound paracetamol sustained-release tablets and chlorpheniramine acid, which is applied in the directions of pharmaceutical formulations, medical preparations containing active ingredients, organic active ingredients, etc., can solve the problem of short half-life, inconvenience in taking medicine, and affecting the therapeutic effect. and other problems, to achieve the effect of reducing toxic side effects, reducing the number of times of medication, and improving compliance

Inactive Publication Date: 2006-02-15
TIANJIN PACIFIC PHARMA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Due to the short half-life of the components, the absorption is fast after oral administration, so the elimination in the body is also fast. In order to maintain the effective blood concentration, three times of daily administration should be taken in a balanced manner, which will cause peaks and valleys in the blood, which will significantly affect the therapeutic effect, and Inconvenient to take medicine

Method used

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  • Compound paracetamol and chlorphenamine maleate slow releasing tablet and its preparation

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0027] Tablet prescription:

[0028] Acetaminophen 375g

[0029] Chlorpheniramine Maleate 4.5g

[0030] Caffeine 22.5g

[0031] Artificial Bezoar 15g

[0032] Carbomer 934P 159g

[0033] Povidone K30 18g

[0034] Magnesium Stearate 3g

[0035] Talc powder 3g

[0036] Preparation process (1) method: paracetamol, chlorpheniramine maleate, caffeine, and artificial bezoar are pulverized and sieved for each use. Povidone K30, magnesium stearate, and talcum powder were sieved separately for subsequent use. Put chlorpheniramine maleate, acetaminophen, caffeine, artificial bezoar, carbomer 934P, povidone K30 in the fluidized bed, mix well, and use absolute ethanol as the wetting agent in the spray In the state, make granules in one step, after drying in a fluidized bed, add magnesium stearate, talcum powder and mix well, then press into tablets, wrap with moisture-proof film, increase in weight by 3%, after drying, discharge the material and dry in a drying room at 40°C for 8 ...

Embodiment 2

[0042] Tablet core prescription

[0043] Acetaminophen 3750g

[0044] Chlorpheniramine Maleate 45g

[0045] Caffeine 225g

[0046] Artificial Bezoar 150g

[0047] Carbomer 934P 159g

[0048] Povidone K30 18g

[0049] Magnesium Stearate 3g

[0050] Talc powder 3g

[0051] Preparation method one: crush and sieve acetaminophen, chlorpheniramine maleate, caffeine, and artificial bezoar for later use. Povidone K30, magnesium stearate, and talcum powder were sieved separately for subsequent use. Put chlorpheniramine maleate, acetaminophen, caffeine, artificial bezoar, carbomer 934P, povidone K30 in the fluidized bed, mix well, and use absolute ethanol as the wetting agent in the spray In the state, make granules in one step, after drying in a fluidized bed, add magnesium stearate and talc powder, mix well, press into tablets, wrap with a moisture-proof film, increase the weight by 3%, discharge after 20 minutes after drying, and dry at 40°C Let it dry indoors for 8 hours. ...

Embodiment 3

[0054] Tablet core prescription

[0055] Acetaminophen 1125g

[0056] Chlorpheniramine Maleate 13.5g

[0057] Caffeine 67.5g

[0058] Artificial Bezoar 45g

[0059] Hypromellose 4KM 477g

[0060] Povidone K30 54g

[0061] Magnesium Stearate 9g

[0062] Talc powder 9g

[0063]Preparation process (1): crush and sieve acetaminophen, chlorpheniramine maleate, caffeine, and artificial bezoar for later use. Povidone K30, magnesium stearate, and talcum powder were sieved separately for subsequent use. Place chlorpheniramine maleate, acetaminophen, caffeine, artificial bezoar, carbomer 934P, and povidone K30 in a fluidized bed, mix well, and mix with absolute ethanol: water (1:1 ) is a wetting agent in a spray state, and it is made into granules in one step. After drying in a fluidized bed, add magnesium stearate and talcum powder, mix well, press into tablets, wrap with a moisture-proof film, increase in weight by 3%, and discharge after drying Dry in a drying room at 40°C f...

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PUM

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Abstract

The invention relates to a compound paracetamol and chlorphenamine slow release tablet and method for preparation, which comprises paracetamol, chlorpheniramine maleate, caffeine, artificial ox gallstone and slow release matrix material, lubricating agent, core and damp-proof membrane consisting binding agent and flow adjuvant, wherein the proportion of the composition is, acetaminopher 30%-80%, chlorpheniramine maleate 0.5%-4%, caffeine 2%-10%, taurine 1%-10%.

Description

technical field [0001] The invention relates to a compound paracetamol sustained-release tablet and a preparation method thereof. Background technique [0002] The granules and capsules for treating colds made of acetaminophen, chlorpheniramine maleate, caffeine, and artificial bezoar composition have been included in the non-prescription drug management range by the state. Due to the short half-life of the components in the composition, the half-life of paracetamol is 75-180 minutes, the half-life of chlorpheniramine maleate is 2-15 hours, and the half-life of caffeine is 3-4 hours. Due to the short half-life of the components, the absorption is fast after oral administration, so the elimination in the body is also fast. In order to maintain the effective blood concentration, three times of daily administration should be taken in a balanced manner, which will cause peaks and valleys in the blood, which will significantly affect the therapeutic effect, and It is inconvenien...

Claims

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Application Information

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IPC IPC(8): A61K31/522A61K9/22A61P31/00A61K31/4402A61K31/167
Inventor 宋德成
Owner TIANJIN PACIFIC PHARMA
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