Antibiotic premixing agent for inhibiting porcine reproductive and respiratory syndrome virus for livestock and preparation method thereof
A technology of premix and mycocin, applied in antiviral agents, pharmaceutical formulations, medical preparations with non-active ingredients, etc., can solve problems such as unfavorable therapeutic effects, increase the number of administrations, and affect animal feed intake, etc., to achieve change Drug release rate, increasing molecular force, increasing the effect of drug dissolution rate
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Embodiment 1
[0037] A veterinary acetylisovaleryl tylosin tartrate premix, the preparation method of which is as follows:
[0038] (1) Stir and mix 10 g of acetylisovaleryl tylosin tartrate API and 10 g of polyacrylic acid resin II for 30 minutes to make a drug-coated carrier mixture;
[0039] (2) Add 0.1g of carboxymethylcellulose, 0.2g of D-sorbitol and 0.4ml of absolute ethanol to the drug-coated carrier mixture obtained in step (1), and continue to stir and mix to obtain a semi-included drug;
[0040] (3) Add 0.05ml of polyethylene glycol 200 dropwise to the half-encapsulated drug in step (2) under stirring to increase the encapsulation efficiency. The complex was washed with water, and then dried in vacuum until the absolute ethanol volatilized completely to obtain a powdered acetylisovaleryl tartrate inclusion compound of tylosin. The measured encapsulation rate was 78.5%, and the drug loading was 25.8%;
[0041] (4) According to the drug loading, add starch to the acetylisovaleryl ...
Embodiment 2
[0043] A veterinary acetylisovaleryl tylosin tartrate premix, the preparation method of which is as follows:
[0044] (1) Mix 10g of acetylisovaleryl tylosin tartrate API with 20g of coating carrier complex (the coating carrier complex is hydroxypropyl-β-cyclodextrin and polyethylene glycol 6000 in a weight ratio of 2:1 The mixture) was stirred and mixed for 30 minutes to make a drug-coated carrier mixture;
[0045] (2) Add 0.3g of carboxymethylcellulose, 0.3g of D-sorbitol and 1.2ml of absolute ethanol to the drug-coated carrier mixture obtained in step (1), and continue to stir and mix to obtain a semi-included drug;
[0046] (3) Add 0.075ml of polyethylene glycol 200 dropwise to the semi-encapsulated drug in step (2) under stirring to increase the encapsulation efficiency. The compound was washed with water, and then dried in vacuum until the absolute ethanol volatilized completely, and the powdery acetylisovaleryl tylosin tartrate inclusion compound was obtained, the enca...
Embodiment 3
[0049] A veterinary acetylisovaleryl tylosin tartrate premix, the preparation method of which is as follows:
[0050] (1) Mix 10g of acetylisovaleryl tylosin tartrate API with 30g of coating carrier complex (the coating carrier complex is hydroxypropyl-β-cyclodextrin and polyethylene glycol 6000 in a weight ratio of 3:1 The mixture) was stirred and mixed for 30 minutes to make a drug-coated carrier mixture;
[0051] (2) Add 0.6 g of carboxymethyl cellulose, 1.6 g of D-sorbitol and 2.0 ml of absolute ethanol to the drug-coated carrier mixture obtained in step (1), and continue to stir and mix to obtain a semi-included drug;
[0052] (3) Add 0.2ml of polyethylene glycol 200 dropwise to the half-encapsulation drug in step (2) under stirring to increase the encapsulation efficiency. The complex was washed with water, and then dried in vacuum until the absolute ethanol volatilized completely, and the powdery acetylisovaleryl tartrate inclusion compound of tylosin was obtained. The...
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