Preparation method of cariprazine-hydrophilic material blend solid preparation
A technology of hydrophilic materials and solid preparations, which is applied in the direction of drug combinations, pharmaceutical formulations, organic active ingredients, etc., and can solve problems that affect the therapeutic effect, are difficult to dissolve, and affect bioavailability
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Embodiment 1
[0012]
[0013] Preparation Process
[0014] Mix cariprazine and 10 times the weight of lactose through an 80-mesh sieve for 3 times, add microcrystalline cellulose and sodium carboxymethyl starch and pass through an 80-mesh sieve for 3 times and mix well, 2% hydroxypropyl cellulose is used as a binder, Granulate with a 24-mesh sieve, air-dry at 50°C, dry to 1-3% moisture, pass the dried granules through a 24-mesh sieve for granulation, weigh, convert the yield, add sodium carboxymethyl starch, aspartame and Magnesium stearate, mix-filled capsules.
Embodiment 2
[0016]
[0017] Preparation Process
[0018] Mix cariprazine and 15 times the weight of mannitol through an 80 mesh sieve for 5 times, add microcrystalline cellulose and pass through an 80 mesh sieve for 3 times and mix evenly, 2% povidone is used as a binder, 30 mesh sieve is granulated, 50 Blow dry at ℃, dry to 1~3% moisture, pass the dried granules through a 30-mesh sieve to sieve, weigh, convert the yield, add sodium carboxymethyl starch, silicon dioxide and mint essence, mix and fill capsules.
Embodiment 3
[0020]
[0021] Preparation Process
[0022] Mix cariprazine and 30 times the weight of lactose through an 80-mesh sieve for 4 times, add the remaining lactose, microcrystalline cellulose and sodium carboxymethyl starch, pass through an 80-mesh sieve for 3 times and mix well, and use 2% povidone as a binder , 24-mesh sieve granulation, blast drying at 50 ℃, drying to 1~3% moisture, passing the dried granules through a 24-mesh sieve for granulation, weighing, conversion yield, plus aspartame, magnesium stearate, Mix filling capsules.
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