Salinomycin sodium suspension as well as preparation method and application thereof
A technology of salinomycin sodium and dry suspension, applied in pharmaceutical formulations, medical preparations with inactive ingredients, medical preparations containing active ingredients, etc., can solve the problem of narrow safety range of salinomycin sodium and poor mixing effect. Ideal, uneven feed mixing, etc., to achieve the effect of improving the scope of clinical application, fast onset of drug effect, and easy storage
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Embodiment 1
[0047] Salinomycin Sodium 2g
[0048] Sucrose 90g
[0050] Methylcellulose 2g
[0051] Glycerin 1g
[0052] The preparation method is as follows:
[0053] (1) accurately weigh the salinomycin sodium of prescription quantity and cross 80 mesh sieves;
[0054](2) Accurately weigh the sucrose, sodium saccharin, and methylcellulose of the prescribed amount respectively, pass through an 80-mesh sieve respectively, and mix uniformly in equal increments;
[0055] (3) Steps (1) and (2) are mixed in equal increments to obtain mixed powder;
[0056] (4) Add 1g of glycerin to the mixed powder to make a soft material, and pass through a 40-mesh sieve;
[0057] (5) Dry at 60°C-80°C, granulate with a 40-mesh sieve;
[0058] (6) After passing the intermediate inspection, the finished product can be obtained by sub-packaging.
Embodiment 2
[0060] Salinomycin Sodium 30g
[0061] Mannose 20g
[0062] Cyclamate 40g
[0063] Hydroxypropyl Methyl Cellulose 20g
[0064] 50 volume% ethanol 30g
[0065] The preparation method is as follows:
[0066] (1) accurately weigh the salinomycin sodium of prescription quantity and cross 120 mesh sieves;
[0067] (2) Accurately weigh the mannose, cyclamate, and hydroxypropyl methylcellulose of the prescription amount respectively, pass through a 120 mesh sieve respectively, and mix uniformly in equal increments;
[0068] (3) Steps (1) and (2) are mixed in equal increments to obtain mixed powder;
[0069] (4) Add 50% ethanol 30g to the mixed powder to make a soft material, and pass through a 30-mesh sieve;
[0070] (5) Dry at 60°C-80°C, and granulate with a 30-mesh sieve;
[0071] (6) After passing the intermediate inspection, the finished product can be obtained by sub-packaging.
Embodiment 3
[0073] Salinomycin Sodium 6g
[0074] Sorbitol 70g
[0075] Acesulfame Potassium 10g
[0076] Polyvinylpyrrolidone 15g
[0077] Propylene glycol 2g
[0078] The preparation method is as follows:
[0079] (1) accurately weigh the salinomycin sodium of prescription quantity and cross 100 mesh sieves;
[0080] (2) Accurately weigh sorbitol, acesulfame potassium, and polyvinylpyrrolidone of the prescribed amount respectively, pass through a 100-mesh sieve respectively, and mix uniformly in equal increments;
[0081] (3) Steps (1) and (2) are mixed in equal increments to obtain mixed powder;
[0082] (4) Add 2 g of propylene glycol to the mixed powder to make a soft material, and pass through a 35-mesh sieve;
[0083] (5) Dry at 60°C-80°C, granulate with a 35-mesh sieve;
[0084] (6) After passing the intermediate inspection, the finished product can be obtained by sub-packaging.
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