Huperzine A pellets preparation and its preparation method
A technology for Huperzine A pellets and Huperzine A, applied in the field of medicine, can solve problems such as low bioavailability, and achieve the effects of high bioavailability, improved drug stability, and uniform size
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Embodiment 1
[0047] Embodiment 1 of the present invention: Huperzine A 10g
[0048] Take huperzine A, add microcrystalline cellulose with a ratio of 1:1000 to the drug powder and starch with a ratio of 1:2000 to the drug powder in the method of progressive dilution, sieve and mix step by step, and add an appropriate amount of ethanol with a concentration of 60%. Wetting agent, HPMC with a concentration of 5% is used as a binder to make soft materials, and then these materials are moved into a pellet machine, extruded into strips through a 1mm sieve, cut into granules, spheronized at a speed of 850r / min, and released Material, drying, with Opadry 2 as coating material, top spray coating: nozzle diameter 1mm, fluidization air volume 100m 3 / h, inlet air temperature 55°C, bed temperature 35°C, atomization pressure 0.15MPa, liquid spray rate 15mL / min, that is, this product is taken orally, twice a day, 1 pack (0.3g) each time.
Embodiment 2
[0049] Embodiment 2 of the present invention: Huperzine A 100g
[0050] After granulating the microcrystalline cellulose, add it to the coating pan, spray it with ethanol with a concentration of 60% to moisten it, roll it into small balls, then wet the mother pellets, then add huperzine A to roll and coat, repeat the operation, The rotating speed of the coating pan is 25r / min, and the preparation time is 10-12 hours. Take out the pan, select the pellets, and coat them. Opadry 2 is used as the coating material. The coating adopts the top spray method: the diameter of the nozzle is 1mm, and the fluidization air volume is 100m 3 / h, inlet air temperature 55°C, bed temperature 35°C, atomization pressure 0.15MPa, liquid spray rate 15mL / min.
Embodiment 3
[0051] Embodiment 3 of the present invention: Huperzine A 50g
[0052] Take huperzine A, mix it with 15% sorbitol, 25% microcrystalline cellulose, and 30% dextrin, and add 8% crospovidone, 10% CCMC -Na, 5% L-HPC, 5% stevioside and an appropriate amount of flavoring agent, mixed evenly, granulated, sized, and compressed into tablets to obtain orally disintegrating tablets.
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