Slow release preparation of Kui-Liu-Ping
A slow-release preparation and preparation technology, which is applied in the directions of inorganic inactive ingredients, non-active ingredients of polymer compounds, inactive ingredients of oil/fat/wax, etc., can solve the problems of short biological half-life, inconvenient use by patients, etc. Or the effect of improving adaptability and reducing the frequency of medication
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Embodiment 1
[0049] The preparation of embodiment 1-quetiapine sustained-release tablet (1)
[0050] Method: Take 100 grams of quetiapine, 50 grams of hydroxypropyl cellulose, 15 grams of hypromellose, 10 grams of lactose, 10 grams of microcrystalline cellulose, 1 gram of carbomer, and 30 grams of polyethylene glycol 4000 , mixed evenly, dry granulated, mixed with magnesium stearate, and compressed into tablets to obtain a finished product with a drug content of 100mg / tablet. Then, the dissolution rate of the quetiapine sustained-release tablet (1) in 900 ml of water at 37° C. was measured. After release measurement, the results are shown in Table 1, which meets the requirements.
[0051] The dissolution rate of table 1 quetiapine sustained-release tablet (1)
[0052] Sampling time (hours)
Embodiment 2
[0053] The preparation of embodiment 2-quetiapine sustained release tablet (2)
[0054] Method: Take 100 grams of quetiapine, 10 grams of hydroxypropyl cellulose, 20 grams of stearyl alcohol, 15 grams of hypromellose, 1 gram of carbomer, and 10 grams of lactose, respectively, pass through 80 mesh sieves, grind and mix Evenly, add a 95% ethanol solution of 10% polyvinylpyrrolidone as a binder and stir to make a soft material, granulate through a 16-mesh sieve, dry the granules at room temperature for 2 hours, granulate with a 16-mesh sieve, and then add stearin Magnesium acid 4.5 grams, micropowder silica gel 2 grams, mix evenly, and tabletting obtains finished product, and containing medicine amount is 100mg / sheet. Then the dissolution rate of the quetiapine sustained-release tablet (2) in 900 ml of water at 37° C. was measured. After release measurement, the results are shown in Table 2, which meets the requirements.
[0055] The dissolution rate of tab...
Embodiment 3
[0057] The preparation of embodiment 3-quetiapine sustained release tablet (3)
[0058] Method: Take 100g of quetiapine, 35g of hypromellose, 5g of microcrystalline cellulose, and 1g of carbomer respectively, pass through 80 mesh sieves, mix well, and add 95% ethanol solution of polyvinylpyrrolidone with a concentration of 10% Used as a binder and stirred to make a soft material, granulated through a 16-mesh sieve, dried at 60°C for 1 hour, granulated with a 16-mesh sieve, then added with 2.5 grams of magnesium stearate, mixed evenly, and pressed into tablets to obtain a finished product, containing drugs The dosage is 100mg / tablet. Then the dissolution rate of the quetiapine sustained-release tablet (3) in 900 ml of water at 37° C. was measured. After release measurement, the results are shown in Table 3, meeting the requirements.
[0059] The dissolution rate of table 3 quetiapine sustained release tablet (3)
[0060] Sampling time (hours)
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