Anti-influenza virus pharmaceutical composition
A compound and dry suspension technology, applied in the field of pharmaceutical preparations, to achieve the effects of improving the operating environment, reducing the loss of raw materials and reducing production costs
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Embodiment 1
[0030] Embodiment 1, the preparation of the oral dry suspension of compound I
[0031] The prescription contents are as follows:
[0032]
[0033]
[0034] Preparation method: First, after crushing the raw and auxiliary materials of the prescription amount respectively, pass through an 80-mesh sieve, and set aside; then mix the compound I of the recipe amount, 33.36% (w / w) sorbitol and xanthan gum evenly to obtain drug granules; then mix the remaining amount of sorbitol, titanium dioxide, orange flavor essence, and sodium saccharin evenly to obtain blank granules; mix the drug-containing granules, blank granules, and sodium benzoate according to the method of equal increments, and pass through a 60-mesh sieve; dry method After granulation, the granules were passed through a 18-mesh sieve for granulation, and then packaged to obtain an oral dry suspension containing Compound I. The content of Compound I was 3 mg / 100 mg.
[0035] Wherein the particle size of compound I D(...
Embodiment 2
[0036] Embodiment 2, the preparation of the oral dry suspension of compound I
[0037] prescription:
[0038]
[0039]
[0040] Preparation method: first, after pulverizing the raw and auxiliary materials of the prescription amount respectively, pass through an 80 mesh sieve, and set aside; then mix the compound I of the prescription amount, 33.40% (w / w) sorbitol and xanthan gum evenly to obtain Then mix the remaining amount of sorbitol, titanium dioxide, sodium dihydrogen citrate, orange flavor essence, and sodium saccharin evenly to obtain blank granules; mix the drug-containing granules, blank granules and sodium benzoate according to the method of equal increments, and pass 60-mesh sieve; after dry granulation, pass through a 18-mesh sieve for sizing, and pack separately to obtain a dry suspension containing Compound I, and the content of Compound I is 5 mg / 100 mg.
[0041] Wherein the particle size of compound I D(v,90)=35 μm.
Embodiment 3
[0042] Embodiment 3, the preparation of the oral dry suspension of compound I
[0043] The prescription contents are as follows:
[0044]
[0045]
[0046] Preparation method: First, after crushing the raw and auxiliary materials of the prescription amount respectively, pass through an 80-mesh sieve, and set aside; then mix the compound I of the recipe amount, 33.36% (w / w) sorbitol and xanthan gum evenly to obtain Then mix the remaining amount of sorbitol, titanium dioxide, sodium dihydrogen citrate, orange flavor essence, and sodium saccharin evenly to obtain blank granules; mix the drug-containing granules, blank granules and sodium benzoate according to the method of equal increments, and pass 60-mesh sieve; after dry granulation, pass through a 18-mesh sieve for sizing, and pack separately to obtain an oral dry suspension containing Compound I, and the content of Compound I is 3 mg / 100 mg.
[0047] Wherein the particle size of compound I D(v,90)=30 μm.
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