Medicinal composition containing pentoxifylline and prucalopride and medical application thereof
A technology of pentoxifylline and a composition, applied in the field of medicine, can solve the problems of inability to effectively improve constipation symptoms, not involving a pharmaceutical composition, lack of outlet obstruction type constipation, etc., achieving broad medical application prospects, improving constipation symptoms, treating full effect
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Embodiment 1
[0035] The preparation of embodiment 1 compound tablet
[0036]
[0037] Preparation process: mix pentoxifylline and prucalopride with auxiliary materials microcrystalline cellulose and starch evenly, add appropriate amount of 15% starch slurry to make soft material, and then granulate through a 16-mesh sieve. Dry the wet granules at 60°C, pass the dry granules through a 16-mesh sieve for granulation, sieve out the fine powder in the dry granules, mix with magnesium stearate, and then mix with the dry granules, and press into tablets to obtain the product.
Embodiment 2
[0038] The preparation of embodiment 2 compound tablet
[0039]
[0040] Preparation process: except that the components are different, the preparation process is the same as that described in Example 1.
Embodiment 3
[0041] Example 3 Preparation of compound bilayer tablet
[0042]
[0043] Preparation process: pentoxifylline is passed through a 100-mesh sieve, hydroxypropyl methylcellulose-4M and microcrystalline cellulose are passed through a 80-mesh sieve, and the prescribed amount of pentoxifylline and hydroxypropyl methylcellulose-4M is weighed , microcrystalline cellulose mixed evenly, adding 8% PVP absolute ethanol solution to granulate in an appropriate amount, drying at 60°C, sieving the dry granules with a 16-mesh sieve, adding magnesium stearate of the prescription amount in the dry granules.
[0044]
[0045] Preparation process: Prucalopride is passed through a 100-mesh sieve, sodium carboxymethylcellulose and lactose are passed through a 80-mesh sieve, the prescribed amount of prucalopride, sodium carboxymethylcellulose and lactose are weighed and mixed evenly, and 6% PVP is added. Appropriate amount of 95% ethanol solution is granulated, dried at 60° C., sieved with 16 ...
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