Intestinal disease treatment pharmaceutical composition and preparation method thereof
A technology of composition and prescription, which is applied in the field of pharmaceutical composition for treating intestinal diseases and its preparation, can solve problems such as incomplete disintegration of polycarbophil calcium, and achieve improved disintegration performance, good disintegration effect, and void space uniform effect
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Embodiment 1
[0046] The formulation of polycarbophil calcium composition:
[0047] calcium polycarbophil
100g
16g
[0048] microcrystalline cellulose
33g
1g
6g
[0049] The preparation method of polycarbophil calcium composition tablet is:
[0050] The croscarmellose sodium and polycarbophil calcium of 50% recipe quantity are mixed at room temperature by equal volume increasing method; the preparation mass concentration is 10% propylene glycol aqueous solution, standby, and 10% propylene glycol aqueous solution is added to the above-mentioned mixture Medium granulation, drying and sizing at 60°C, then adding the remaining amount of croscarmellose sodium, prescription amount of microcrystalline cellulose, and magnesium stearate to it, and finally compressing into tablets to obtain tablets .
Embodiment 2
[0052] The prescription is the same as in Example 1, and the preparation method is: the croscarmellose sodium and polycarbophil calcium of 50% recipe quantity are mixed at room temperature by an equal increase method; the preparation mass concentration is 10% propylene glycol aqueous solution, Standby, add 10% propylene glycol aqueous solution to the above mixture to granulate, dry and granulate at 60°C, then add the remaining amount of croscarmellose sodium and the prescribed amount of microcrystalline cellulose, hard Magnesium steatate, filled capsules, to obtain calcium polycarbophil capsules.
Embodiment 3
[0054] The prescription is the same as in Example 1, and the preparation method is: the croscarmellose sodium and polycarbophil calcium of 50% recipe quantity are mixed at room temperature by an equal increase method; the preparation mass concentration is 10% propylene glycol aqueous solution, Standby, add 10% propylene glycol aqueous solution to the above mixture to granulate, dry and granulate at 60°C, then add the remaining amount of croscarmellose sodium and the prescribed amount of microcrystalline cellulose, hard Magnesium fatty acid, finally divided into granules.
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