A kind of microencapsulated animal drug and preparation method thereof
A technology for medicines and animals, applied in microcapsules, pharmaceutical formulations, inactive components of polymer compounds, etc. It can solve the problems of inapplicability of easily oxidized and heat-sensitive materials, inability to meet the requirements of assembly lines, and irregular product particles. , to achieve good market prospects, improve production efficiency, and achieve the effect of particle rounding
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Embodiment 1
[0033] Embodiment 1, microencapsulated animal drug of the present invention and preparation method thereof
[0034] Formula: tilmicosin 25kg, gelatin 30kg, sucrose 40kg, Tween-80 5kg, corn starch 30kg, microcrystalline cellulose 3kg;
[0035] Preparation:
[0036] S1. Preparation of wall materials: dissolve gelatin and sucrose in 200 kg of water to obtain water phase A;
[0037] S2, preparation of capsule material: dissolve tilmicosin in 300kg water, then add Tween-80 to obtain oil phase B;
[0038] S3. Preparation of dispersion system: under the conditions of shear power of 50kW and stirring speed of 10000r / min, the oil phase B was added to the water phase A, and then the stirring time was 15min and the temperature was 50°C Under certain conditions, part of the water is removed to form a microemulsion;
[0039] S4, spray granulation and drying: in the spray granulation tower, add the mixed filler of the cornstarch of formula quantity and microcrystalline cellulose, then pu...
Embodiment 2
[0041] Embodiment 2, microencapsulated animal drug of the present invention and preparation method thereof
[0042] Formula: tiamulin fumarate 30kg, gelatin 30kg, glucose 35kg, Tween-80 5kg, corn starch 40kg, microcrystalline cellulose 8kg;
[0043] Preparation:
[0044] S1. Preparation of wall materials: dissolve gelatin and glucose in 200 kg of water to obtain water phase A;
[0045] S2. Preparation of capsule material: dissolve tiamulin fumarate in 400 kg of ethanol with a volume fraction of 85%, and then add Tween-80 to obtain oil phase B;
[0046] S3. Preparation of dispersion system: under the conditions of shear power of 50kW and stirring speed of 5000r / min, the oil phase B was added to the water phase A, and then the stirring time was 15min and the temperature was 50°C Under the conditions, ethanol is removed to form a microemulsion;
[0047] S4, spray granulation and drying: in the spray granulation tower, add the mixed filler of the cornstarch of formula quantity an...
Embodiment 3
[0049] Embodiment 3, microencapsulated animal drug of the present invention and preparation method thereof
[0050] Formula: enrofloxacin sodium 25kg, gelatin 30kg, sucrose 40kg, Tween-80 5kg, rice bran 35kg, microcrystalline cellulose 5kg;
[0051] Preparation:
[0052] S1. Preparation of wall materials: dissolve gelatin and sucrose in 200 kg of water to obtain water phase A;
[0053] S2. Preparation of capsule material: dissolving enrofloxacin sodium in 300kg of water, then adding Tween-80 to obtain oil phase B;
[0054] S3. Preparation of dispersion system: under the conditions of shear power of 80kW and stirring speed of 5000r / min, the oil phase B was added to the water phase A, and then the stirring time was 20min and the temperature was 50°C Under certain conditions, part of the water is removed to form a microemulsion;
[0055] S4. Spray granulation and drying: Add the mixed filler of rice bran and microcrystalline cellulose in the formula amount into the spray granu...
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