Metroprolol succinate sustained-release tablets and preparation method thereof
A technology of metoprolol succinate and sustained-release tablets, which can be applied in pharmaceutical formulations, medical preparations with inactive ingredients, cardiovascular system diseases, etc., and can solve problems such as sudden drug release, large environmental pollution, and solvent solvent residues , to achieve the effect of improving production efficiency
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Embodiment 1
[0029] Metoprolol Succinate Extended Release Tablets
[0030] Material name percentage(%) Silica blank ball core 15.0 metoprolol succinate 19.0 Aqueous dispersion of ethyl cellulose (solid content) 7.2 Ethyl cellulose 37.2 Hydroxyethyl cellulose 18.6 Micropowder silica gel 3.0 total 100.0
[0031] According to the prescription ratio, weigh the prescription amount of silica blank pellet core (100~200μm), metoprolol succinate (d 0.9 =34μm), ethyl cellulose (d 0.9 =16μm), hydroxyethyl cellulose was premixed and set aside. At the same time, dilute the ethylcellulose aqueous dispersion to a concentration of 10-15% with purified water. Open the fluidized bed top spray one-step granulator, put the premixed material into the granulator, start the preheating step, preheat for a period of time, when the product temperature reaches 30℃~35℃, spray diluted ethyl alcohol The cellulose-based aqueous dispersion solution is used for g...
Embodiment 2
[0033] Metoprolol Succinate Extended Release Tablets
[0034] Material name percentage(%) Silica blank ball core 15.0 metoprolol succinate 19.0 Aqueous dispersion of ethyl cellulose (solid content) 7.2 Ethyl cellulose 37.2 Hydroxyethyl cellulose 18.6 Micropowder silica gel 3.0 total 100.0
[0035] In embodiment 2, prescription is identical with embodiment 1, and difference is that metoprolol succinate d 0.9 =12μm, ethyl cellulose d 0.9 = 8 μm, using the same preparation process as in Example 1 to granulate, the recovery rate in the granulation process was 90.1%, which was significantly lower than the recovery rate reported in Example 1, showing that it is very necessary to control the particle size of the material .
Embodiment 3
[0037] Metoprolol Succinate Extended Release Tablets
[0038] Material name percentage(%) Silica blank ball core 10.0 metoprolol succinate 19.0 Aqueous dispersion of ethyl cellulose (solid content) 8.0 Ethyl cellulose 41.0 Hydroxyethyl cellulose 20.5 Micropowder silica gel 1.5 total 100.0
[0039] Using the same preparation process in Example 1, the prepared sustained-release tablets were compared with the commercially available products of AstraZeneca for dissolution in vitro, f 2 =57, proving that the dissolution of the two is consistent.
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