Ibuprofen and lysine medicament compound as well as preparation method and application thereof
A technology of lysine and composition, which is applied to the pharmaceutical composition of ibuprofen and lysine and the field of preparation thereof, can solve the problems of affecting the scope of application and clinical effect, being difficult to be prepared into oral solution preparations and injections, etc. The effect of improving production efficiency and simplifying the preparation process
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Embodiment 1
[0014] prescription:
[0015] Ibuprofen: 100g
[0016] Lysine: 78g
[0017] Water for injection 1000ml
[0018] Preparation method: According to the process of small-capacity injection, first dissolve lysine in about 800ml of water, add ibuprofen while stirring until it is completely dissolved, add water for injection to 1000ml; absorb with activated carbon, decarbonize, followed by 0.45 micron, 0.22 micron microporous membrane filtration; after the filtrate content is qualified, it is filled in a washed, dried and sterilized ampoule, and melted; sterilized at 115°C for 30 minutes to make a finished product.
Embodiment 2
[0020] prescription:
[0021] Ibuprofen: 100g
[0022] Lysine: 78g
[0023] Water for injection 1000ml
[0024] Preparation method: According to the process of small-volume injection, mix ibuprofen and lysine, add about 800ml of water for injection, stir until it is completely dissolved, add water for injection to 1000ml; 0.45 micron, 0.22 micron microporous membrane filtration; after the filtrate content is qualified, it is filled in a washed, dried and sterilized ampoule, and melted; sterilized at 115°C for 30 minutes to make a finished product.
Embodiment 3
[0026] prescription:
[0027] Ibuprofen: 100g
[0028] Lysine: 78g
[0029] Water for injection 1000ml
[0030] Preparation method: According to the preparation process of oral liquid, first dissolve lysine in about 800ml of water, add ibuprofen while stirring until completely dissolved, add flavoring agent, etc., add water for injection to 1000ml, filter After the determination of the filtrate content is qualified, it is filled in the oral liquid bottle that has been washed, dried and sterilized, and sealed; sterilized at 115° C. for 30 minutes to make a finished product.
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