A kind of levetiracetam sustained-release tablet and preparation method thereof
A technology of sustained-release tablet and sustained-release layer, which is applied in the field of levetiracetam sustained-release tablet and its preparation, and can solve the problems of ineffectiveness and the like
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0031] 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: take 200 g of glyceryl behenic acid and 15 g of polyvinylpyrrolidone K3015 g and mix them uniformly in equal increments. Granulation by method, weighing; Preparation of drug-containing sustained-release layer: levetiracetam 500g, glyceryl behenate 150g, polyvinylglycerol 150g, polyvinylpyrrolidone K3020g are mixed with equal increments, dry granulation, Weighing; tableting: add 1% magnesium stearate to the blank layer and the drug-containing layer and mix them evenly, separate them into two hoppers and compress them into 1000 tablets on a double-layer tablet press. Each tablet contains 500mg of levetiracetam.
Embodiment 2
[0033] First, put the raw materials and auxiliary materials at 60°C and dry them for 4 hours, pass through an 80-mesh sieve for later use; then, prepare a blank layer: take 300 g of ethyl cellulose and 15 g of polyvinylpyrrolidone K3015 g and mix them uniformly in equal increments, and wet-process Granules, weighed; preparation of drug-containing sustained-release layer: levetiracetam 500g, ethyl cellulose 200g, polyvinylpyrrolidone K3020g were mixed in equal increments, wet granulated, weighed; tabletting: the blank Add 1% magnesium stearate to the layer and the drug-containing layer and mix evenly, separate the two hoppers and compress it into 1000 tablets on a double-layer tablet press. Each tablet contains 500mg of levetiracetam.
Embodiment 3
[0035] 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: take 180 g of hypromellose and 20 g of polyvinylpyrrolidone K3020 g and mix them uniformly in an equal increment method, dry Granulation by method, weighing; preparation of drug-containing sustained-release layer: levetiracetam 500g hypromellose 150g, polyvinylpyrrolidone K30 20g were mixed with the same amount increasing method, dry granulation, weighing; tabletting: the The blank layer and the drug-containing layer are respectively added with 1% magnesium stearate and mixed evenly, separated into two hoppers and compressed into 1000 tablets on a double-layer tablet press. Each tablet contains 500mg of levetiracetam.
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com