Pharmaceutical composition for improving osteoarticular diseases, disintegrating tablets and preparation method of pharmaceutical composition
A technology for bone and joint diseases and compositions, which is applied in the field of pharmaceutical compositions for improving bone and joint diseases, and can solve problems such as insignificant drug effects and slow onset of bone and joint diseases
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Embodiment 1
[0039] Formula: 95 parts of glucosamine, 15 parts of taurine, 20 parts of microcrystalline cellulose, 15 parts of crospovidone, 10 parts of xylitol, 5 parts of hydroxypropyl methylcellulose, 2.8 parts of talc, micronized 2.8 parts of silica gel, 1.4 parts of magnesium stearate.
[0040] Process: Weigh each raw material according to the prescription, crush glucosamine, taurine, microcrystalline cellulose, xylitol and partially cross-linked povidone, mix them evenly, put them in a mixer, and add hydroxypropyl methylcellulose , and stir evenly to make a soft material. Extrude the soft material through the sieve to make granules, or pass the soft material through the sieve twice to make the granules more uniform and less fine powder. Place the wet granules in a desiccator to remove excess moisture from the granules. Arranging the dried granules to disperse the agglomerated and cohesive granules to obtain granules of uniform size. After the granulation is completed, add talcum p...
Embodiment 2
[0042] Formula: 95 parts of glucosamine, 25 parts of taurine, 20 parts of microcrystalline cellulose, 15 parts of crospovidone, 10 parts of xylitol, 8 parts of hydroxypropyl methylcellulose, 2.8 parts of talcum powder, micronized 2.8 parts of silica gel, 1.4 parts of magnesium stearate.
[0043] Disintegrating tablets were prepared according to the same preparation process as in Example 1.
Embodiment 3
[0045] Formula: 105 parts of glucosamine, 15 parts of taurine, 25 parts of microcrystalline cellulose, 18 parts of crospovidone, 16 parts of xylitol, 7 parts of hydroxypropyl methylcellulose, 4 parts of talc, micronized 4 parts of silica gel, 2 parts of magnesium stearate.
[0046] Disintegrating tablets were prepared according to the same preparation process as in Example 1.
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