Solid dispersible granule for treating peptic ulcer
A peptic ulcer and solid dispersion technology, which is applied to the digestive system, medical preparations containing active ingredients, plant/algae/fungus/moss components, etc., can solve the problems of high cost, high medicinal taste, and large amount of medicinal materials. Enhanced anti-ulcer activity, good analgesic effect, and improved bioavailability
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Embodiment 1
[0027] The preparation of embodiment 1 pharmaceutical composition of the present invention
[0028] Zushima 3g, Anisopolamine 0.5g, Dried Ginger 9g, Seabuckthorn 10g; after drying, crush to 300 mesh, mix evenly to get raw material medicine powder.
[0029] Take raw drug powder: polyethylene glycol-6000=1:1w / w, mix well, heat until polyethylene glycol-6000 is in a molten state, stir, immediately place in 0°C environment and quench until solidified, crush to obtain Solid dispersion.
[0030] Take the solid dispersion: dextrin = 1:1w / w, use water as the binder, and wet granulate to obtain solid dispersion granules.
Embodiment 2
[0031] The preparation of embodiment 2 pharmaceutical compositions of the present invention
[0032] Zushima 1g, Anisopolamine 0.6g, Dried Ginger 6g, Seabuckthorn 10g; after drying, crush to 400 mesh, mix evenly to get the raw material medicine powder.
[0033] Take raw drug powder: polyethylene glycol-6000=1:3w / w, mix well, heat until polyethylene glycol-6000 is in a molten state, stir, immediately place in 0°C environment and quench until solidified, crush to obtain Solid dispersion.
[0034] Take solid dispersion: starch=1:3w / w, use starch slurry as binder, wet granulate to obtain solid dispersion granules.
Embodiment 3
[0035] The preparation of embodiment 3 pharmaceutical composition of the present invention
[0036] Zushima 1g, anisopolamine 0.3g, dried ginger 10g, seabuckthorn 6g; after drying, crush into 500 meshes, and mix well to obtain the raw material medicine powder.
[0037] Take raw drug powder: polyethylene glycol-6000=3:1w / w, mix well, heat until polyethylene glycol-6000 is in a molten state, stir, immediately place in 0°C environment and quench until solidified, pulverize to obtain Solid dispersion.
[0038] Take solid dispersion: microcrystalline cellulose: dextrin = 1:1:1 w / w, use 70% v / v ethanol as binder, and wet granulate to obtain solid dispersion granules.
[0039] The beneficial effects of the present invention are further demonstrated through specific test examples below.
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