Medicinal composition containing pimobendan and preparation method of medicinal composition
A technology of pimobendan and its composition, which is applied in the field of pimobendan-containing pharmaceutical composition and its preparation, can solve the problem of low solubility of pimobendan, achieve strong vasodilation and platelet aggregation, Improved solubility and good stability
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Embodiment 1
[0037]
[0038]
[0039] Preparation:
[0040] a) uniformly mix pimobendan and anhydrous citric acid in a ratio of 1:20, and ultrafinely pulverize them in an ultrafine pulverizer to obtain a micronized mixture with a particle size of 200 mesh;
[0041] b) Other ingredients are passed through a 100-mesh sieve respectively, and set aside;
[0042] c) mix a) with cornstarch, microcrystalline cellulose, 75% low-substituted hydroxypropyl cellulose, and beef powder in equal increments;
[0043] d) adding an aqueous solution of hypromellose to c) to make a soft material;
[0044] e) Perform wet granulation of the prepared soft material, dry at 65°C until the moisture content of the granules is about 3%, and granulate;
[0045] f) Add 25% low-substituted hydroxypropyl cellulose to e), and mix well;
[0046] g) adding micropowder silica gel and magnesium stearate to f), and mixing uniformly;
[0047] h) Compressing the obtained g) into tablets.
Embodiment 2
[0049]
[0050] Preparation:
[0051] a) uniformly mix pimobendan and anhydrous citric acid in a ratio of 1:20, and ultrafinely pulverize them in an ultrafine pulverizer to obtain a micronized mixture with a particle size of 400 mesh;
[0052] b) Other ingredients are passed through a 100-mesh sieve respectively, and set aside;
[0053] c) mix a) with cornstarch, microcrystalline cellulose, 75% low-substituted hydroxypropyl cellulose, and beef powder in equal increments;
[0054] d) adding an aqueous solution of hypromellose to c) to make a soft material;
[0055] e) Perform wet granulation of the prepared soft material, dry at 65°C until the moisture content of the granules is about 3%, and granulate;
[0056] f) Add 25% low-substituted hydroxypropyl cellulose to e), and mix well;
[0057] g) adding micropowder silica gel and magnesium stearate to f), and mixing uniformly;
[0058] h) Compressing the obtained g) into tablets.
Embodiment 3
[0060]
[0061] Preparation:
[0062] a) uniformly mix pimobendan and anhydrous citric acid according to the ratio of 1:20, and ultrafinely pulverize them in an ultrafine pulverizer to obtain a micronized mixture with a particle size of 300 mesh;
[0063] b) Other ingredients are passed through a 100-mesh sieve respectively, and set aside;
[0064] c) mix a) with cornstarch, microcrystalline cellulose, 75% low-substituted hydroxypropyl cellulose, and beef powder in equal increments;
[0065]d) adding an aqueous solution of hypromellose to c) to make a soft material;
[0066] e) Perform wet granulation of the prepared soft material, dry at 65°C until the moisture content of the granules is about 3%, and granulate;
[0067] f) Add 25% low-substituted hydroxypropyl cellulose to e), and mix well;
[0068] g) adding micropowder silica gel and magnesium stearate to f), and mixing uniformly;
[0069] h) Compressing the obtained g) into tablets.
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