Veterinary enrofloxacin flavor tablet and preparation method thereof
A technology of enrofloxacin and tablets, which is applied in the field of veterinary enrofloxacin flavored tablets and its preparation, can solve the problems of unsuitability for large-scale production of veterinary drugs, economic losses in pig breeding industry, high process costs, etc.
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Embodiment 1
[0132] The screening of solid dispersion carrier material in the enrofloxacin flavor tablet of embodiment 1 veterinary
[0133] Weigh 2.4g of the solid dispersion material as described in Table 1 and melt at 100°C, then add a small amount of enrofloxacin powder of known mass several times under continuous stirring, and stir for 30 minutes after adding until the carrier material solution Can no longer dissolve more enrofloxacin (and reach saturation), write down the mass of enrofloxacin added at this time, and calculate the maximum solubility of enrofloxacin in the solid dispersion material. See Table 1 for the maximum solubility of enrofloxacin in selected solid dispersion carrier materials (100°C, 30min). In order to ensure the stability of the prepared enrofloxacin flavor tablet and the high drug content of the product, cetyl palmitate was selected as the solid dispersion material in the formula.
[0134] Solubility of table 1 enrofloxacin in carrier material
[0135]
Embodiment 2
[0136] Example 2 Enrofloxacin flavored tablets for veterinary use are used for preparation process optimization of tablet granules
[0137] A kind of prescription (see Table 2) that is used for tableting granule in the veterinary enrofloxacin flavor tablet of the present invention.
[0138] Table 2 Recipe of Tablet Granules
[0139]
[0140]
[0141] Prepare as follows:
[0142] 1) 40 g of cetyl palmitate was heated and dissolved, then 7 g of enrofloxacin was added, and stirred to dissolve enrofloxacin in the molten cetyl palmitate to obtain solution 1;
[0143] 2) Pour solution 1 onto a cold stainless steel plate, cool and solidify for 30 minutes to obtain a solid dispersion of enrofloxacin, and pulverize the resulting solid dispersion with a pulverizer to obtain a solid dispersion of enrofloxacin with a particle size of 200 μm-800 μm body powder;
[0144] 3) After weighing 30 g of microcrystalline cellulose and 20 g of malic acid and mixing them evenly with the powd...
Embodiment 3
[0147] Example 3 Screening of prescription 1 of enrofloxacin flavor tablet for veterinary use
[0148] The design of prescription 1 of the veterinary enrofloxacin flavor tablet of the present invention is shown in Table 3.
[0149] Table 3 Composition 1 of enrofloxacin flavor tablet for veterinary use
[0150]
[0151] Prepare as follows:
[0152] 1) Heat and dissolve 40 g of cetyl palmitate, add 5 g of enrofloxacin, and stir to completely dissolve enrofloxacin in the molten cetyl palmitate to obtain solution 1.
[0153] 2) Pour solution 1 onto a cold stainless steel plate, cool and solidify for 30 minutes to obtain a solid dispersion of enrofloxacin, and pulverize the resulting solid dispersion with a pulverizer to obtain a solid dispersion of enrofloxacin with a particle size of 200 μm-600 μm body powder.
[0154] 3) After weighing 30g of microcrystalline cellulose and 21.5g of sucrose and mixing them evenly with the powder in step 2), add the 10% (3g→30mL) polyvinylpy...
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