Medicinal composition containing carbazochrome sodium sulfonate compound and preparation method thereof
A technology of sodium carbosulfonate and its composition, which is applied in the field of pharmaceutical compositions containing sodium carbosulfonate and its preparation, can solve the problems of poor stability and difficulty in long-term storage, and achieve the effect of overcoming poor stability
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Embodiment 1
[0021] 1. Formula (weight: g): sodium carbosulfate 1, mannitol 0.1, dextran 2 and sodium hydroxide 0.5.
[0022] 2. Preparation method:
[0023] 1) Add the prescribed amount of sodium carbosulfonate, mannitol and dextran into an appropriate amount of water for injection, and stir until completely dissolved to obtain solution A;
[0024] 2) adding sodium hydroxide into an appropriate amount of water for injection to dissolve, then adding the sodium hydroxide solution into solution A, stirring evenly, so that the pH value of the mixed solution is 5, and obtaining solution B;
[0025] 3) Add activated carbon with a prepared volume of 0.5% to solution B, boil for 30 minutes, filter and decarbonize, collect the filtrate, and then sterilize and filter with a 0.2 μm microporous membrane to collect filtrate C;
[0026] 4) The filtrate C is freeze-dried to make a powdery pharmaceutical composition.
Embodiment 2
[0028] 1. Formula (weight: g): sodium carbosulfonate 1, mannitol 1, dextran 8 and sodium hydroxide 2.
[0029] 2. Preparation method:
[0030] 1) Add the prescribed amount of sodium carbosulfonate, mannitol and dextran into an appropriate amount of water for injection, and stir until completely dissolved to obtain solution A;
[0031] 2) adding sodium hydroxide into an appropriate amount of water for injection to dissolve, then adding the sodium hydroxide solution into solution A, stirring evenly, so that the pH of the mixed solution is 6, and obtaining solution B;
[0032] 3) Add activated carbon with a prepared volume of 0.5% to solution B, boil for 30 minutes, filter and decarbonize, collect the filtrate, and then sterilize and filter with a 0.2 μm microporous membrane to collect filtrate C;
[0033] 4) The filtrate C is freeze-dried to make a powdery pharmaceutical composition.
Embodiment 3
[0035] 1. Formula (weight: g): sodium carbosulfonate 1, mannitol 0.6, dextran 6 and sodium hydroxide 1.
[0036] 2. Preparation method:
[0037] 1) Add the prescribed amount of sodium carbosulfonate, mannitol and dextran into an appropriate amount of water for injection, and stir until completely dissolved to obtain solution A;
[0038] 2) Dissolve sodium hydroxide in an appropriate amount of water for injection, then add the sodium hydroxide solution into solution A, stir evenly, make the pH of the mixed solution 5.5, and obtain solution B;
[0039] 3) Add activated carbon with a prepared volume of 0.5% to solution B, boil for 30 minutes, filter and decarbonize, collect the filtrate, and then sterilize and filter with a 0.2 μm microporous membrane to collect filtrate C;
[0040] 4) The filtrate C is freeze-dried to make a powdery pharmaceutical composition.
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