Medicine composition containing sodium L-ascorbate and preparing method of medicine composition
A vitamin and composition technology, applied in the field of pharmaceutical composition and its preparation, can solve problems affecting human health, unstable preparations, adverse reactions, etc., and achieve the effects of reducing the risk of medication, easy operation, and definite curative effect
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Embodiment 1
[0028] The preparation method of the pharmaceutical composition tablet containing sodium vitamin C comprises the steps:
[0029] S1: Weigh the components according to the following weights: 75 parts of sodium vitamin C, 5 parts of potassium chloride, 1 part of starch, 1 part of sucrose, and 0.5 parts of maltodextrin;
[0030] S2: Crush sodium vitamin C, potassium chloride, starch, sucrose, and maltodextrin into fine powders, and pass through an 80-mesh sieve;
[0031] S3: The sieved fine powder is mixed evenly, granulated, dried, granulated, and tabletted to obtain the product.
Embodiment 2
[0033] The preparation method of the pharmaceutical composition tablet containing sodium vitamin C comprises the steps:
[0034] S1: Weigh the components according to the following weights: 95 parts of sodium vitamin C, 10 parts of potassium chloride, 1.5 parts of starch, 2 parts of sucrose, and 1 part of maltodextrin;
[0035] S2: Crush sodium vitamin C, potassium chloride, starch, sucrose, and maltodextrin into fine powders, and pass through an 80-mesh sieve;
[0036] S3: The sieved fine powder is mixed evenly, granulated, dried, granulated, and tabletted to obtain the product.
[0037] Two, the preparation method that contains vitamin C sodium sterile powder injection
Embodiment 3
[0039] The preparation method of sodium aseptic powder containing vitamin C comprises the following steps:
[0040] S1. Weigh 85 parts of sodium vitamin C and 8 parts of potassium chloride;
[0041] S2. Add the weighed vitamin C sodium and potassium chloride into the water for injection, stir to dissolve it, and obtain a mixed solution;
[0042] S3. The mixed solution is filtered with a microporous membrane with a pore size of 0.22um, and then filtered through a 0.01um ultrafiltration membrane to remove impurities, bacteria and heat sources to obtain a medicinal solution;
[0043] S4. The medicinal solution is spray-dried at a low temperature of 50°C under aseptic conditions to obtain sterile powder, which is then quantitatively dispensed into vials under aseptic conditions, and packed with stoppers and caps.
[0044] Take 1 g of the prepared sample of Example 3, add 10 ml of water at room temperature to dissolve, the sample solution is clear, free of particles, and the measu...
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