Florfenicol taste masking preparation and preparation method for same
A preparation technology of florfenicol, which is applied in the field of veterinary antibiotic preparations, can solve the problems of florfenicol bitter taste and poor palatability, etc., and achieve the effect of simple and reliable preparation process
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Embodiment 1
[0050] Mix Florfenicol (10%), starch (37.5%), and microcrystalline cellulose (37.5%) evenly to obtain a physical mixture; then dissolve Eudragit E100 (15%) in 60% ethanol aqueous solution, Add to the physical mixture to make soft material, granulate with a swing granulator, pass through a 20-mesh sieve to obtain wet granules, dry at 50°C, and granulate with a 18-mesh sieve. The dissolution of the drug in water was 1.6% in 1 minute, and 7.2% in 10 minutes; the dissolution of the drug in 0.1mol / L hydrochloric acid was 81.5% in 2 minutes, and the dissolution was complete in 10 minutes.
[0051] With reference to the Chinese Pharmacopoeia 2010 edition two appendix X C the third method detects drug dissolution rate, draws dissolution curve, such as figure 1 shown. Dissolution medium: 250 ml deionized water or 0.1molL -1 Hydrochloric acid solution, speed: 100rpm / min, temperature: 37.0°C±0.5°C, sample 6ml at 0.33, 0.67, 1, 2, 5, 8, 10, 20, 30, 45, 60min, and supplement the same vol...
Embodiment 2
[0053] Mix Florfenicol (10%), starch (51%), and Eudragit EPO (30.5%) evenly to obtain a physical mixture; then dissolve Eudragit E100 (8.5%) in 70% ethanol aqueous solution, Add to the physical mixture to make soft material, granulate with a swing granulator, pass through a 65-mesh sieve to obtain wet granules, and dry at 50°C to obtain the product. The dissolution rate of the drug in water was 8.6% in 1 minute, 71.6% in 1 minute in 0.1 mol / L hydrochloric acid, and 94.7% in 5 minutes.
Embodiment 3
[0055] Mix florfenicol (10%), lactose (20%), low-substituted hydroxypropyl cellulose (10%), and microcrystalline cellulose (45%) to obtain a physical mixture; then Eudragit E100 ( 15%) dissolved in 60% ethanol aqueous solution, added to the physical mixture to make a soft material, passed through a 0.5mm aperture sieve, extruded through a screw extruder to make strips, and placed in a rounding equipment for 2 minutes to obtain pellets , 55 ℃ drying, that is. The dissolution of the drug in water was 3.0% in 1 minute, and 9.3% in 5 minutes; the dissolution of the drug in 0.1mol / L hydrochloric acid water reached 81.6% in 20 minutes, and was greater than 90% in 30 minutes.
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