Compound preparation containing ribavirin and new decanoy acetaldehyde sodium and its preparation method
A new technology for sodium houttuyniacin and compound preparation, which can be applied in the field of medicine and can solve the problems of large toxic and side effects, limited wide application and the like
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Embodiment 1
[0018] Example 1 (freeze-dried powder for injection): take the prescribed amount of Houttuyfonate Sodium, add 14000ml of water for injection, heat to 70-80°C and stir to dissolve until clear; take another prescribed amount of ribavirin plus 6000ml of water for injection , heated and stirred to dissolve. After mixing the above two solutions, add the prescribed amount of Dextran S 40 , heated and stirred until the solution was clear. Add 20g of activated carbon, stir and adsorb for 30 minutes, filter to remove carbon, and adjust the pH to 6.0 with hydrochloric acid (1→10) solution. Filter through a 0.22μm microporous membrane, measure the content, and pack in 2.0ml each. It can be obtained by freeze-drying. Freeze-drying conditions: vacuum degree 750mmHg, pre-freezing temperature -40°C, pre-freezing time 2 hours; sublimation temperature -20°C, sublimation time 10 hours; first drying temperature 20°C, drying time 4 hours; second drying temperature 40 ℃, drying time 6 to 8 hour...
Embodiment 2
[0019]Embodiment 2 (powder for injection) In the aseptic operation room, take ribavirin and neohouttuycin sodium of the prescription amount, fully mix, and aseptically pack in 10ml vials, seal, press Aluminum cover will do.
Embodiment 3
[0020] Example 3 (injection) Take by weighing the prescribed amount of ribavirin and neohouttuyfonate sodium, add the prescribed amount of houttuyfonate sodium, add 14000ml of water for injection, heat to 70-80°C and stir to dissolve until clear; Prescribed amount of ribavirin plus water for injection 6000ml, heated and stirred to dissolve. After mixing the above two solutions, heat and stir until the solution becomes clear. Add 20g of activated carbon, stir and adsorb for 30 minutes, filter to remove carbon, and adjust the pH to 6.0 with hydrochloric acid (1→10) solution. Filter through a 0.22μm microporous membrane, measure the content, and pack in aliquots.
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