A Chinese veterinary drug composition for improving body immunity and its preparation method and application
A technology of immunity and use, applied in the direction of drug combination, pharmaceutical formula, medical preparations containing active ingredients, etc., can solve the problems of extensive preparation, difficult quality control, large dosage, etc., and achieve simple preparation process and low production cost. Inexpensive, dissolution-enhancing effect
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Embodiment 1
[0023] The preparation of embodiment 1 pharmaceutical particle of the present invention
[0024] Get 10kg of Radix Astragali, 10kg of Rhizoma Polygonatum, and 10kg of Curcuma longa, dry the two herbs until the moisture is 6%-8%, pulverize them with a hammer mill to 100 mesh and mix them uniformly for later use. Take the uniformly mixed 80-mesh drug powder and grind it to 500-2000 mesh with an ultrafine pulverizer. This process must be carried out at -20°C to -30°C to prevent polysaccharides from melting and bonding and damage to active ingredients. Finally, dry the obtained ultrafine powder into coarse particles to obtain the drug granules of the present invention.
Embodiment 2
[0025] The preparation of embodiment 2 pharmaceutical granules of the present invention
[0026] Get 5kg of Radix Astragali, 10kg of Polygonatum, and 15kg of Turmeric, dry the two medicines until the moisture is 6%-8%, pulverize them with a hammer mill to 100 mesh and mix them uniformly for later use. Take the uniformly mixed 80-mesh drug powder and grind it to 500-2000 mesh with an ultrafine pulverizer. This process must be carried out at -20°C to -30°C to prevent polysaccharides from melting and bonding and damage to active ingredients. Finally, dry the obtained ultrafine powder into coarse particles to obtain the drug granules of the present invention.
Embodiment 3
[0027] The preparation of embodiment 3 pharmaceutical granules of the present invention
[0028] Get 15kg of Radix Astragali, 10kg of Rhizoma Polygonatum, and 5kg of Curcuma Longa, dry the two herbs until the water content is 6%-8%, pulverize them with a hammer mill to 100 mesh and mix them uniformly for later use. Take the uniformly mixed 80-mesh drug powder and grind it to 500-2000 mesh with an ultrafine pulverizer. This process must be carried out at -20°C to -30°C to prevent polysaccharides from melting and bonding and damage to active ingredients. Finally, dry the obtained ultrafine powder into coarse particles to obtain the drug granules of the present invention.
[0029] The hammer mill model used in the embodiment is Jishou City Zhongcheng Pharmaceutical Machinery Factory LH-08B, the model of the ultrafine pulverizer: Bailey BFM-6, in addition to the equipment described in the present invention, other models can also be used device of.
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