A kind of pharmaceutical composition and application thereof for treating diabetes and its complications
A composition and complication technology, applied in the field of medicine, can solve the problems of edema, weight gain, increased insecurity, insulin resistance, etc., and achieve the effects of reducing hypertension, reducing incidence, and reducing blood sugar
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Embodiment 1
[0043] Embodiment 1 Compound pioglitazone bromocriptine tablet
[0044]
[0045] Preparation process: Weigh the bromocriptine, pioglitazone, starch, dextrin and low-substituted hydroxypropyl cellulose in the prescribed amount and mix them evenly. Another appropriate amount of 60% ethanol is added to the mixed powder, mixed evenly to make a soft material, granulated through a 16-mesh sieve, and dried below 60°C. After the drying is completed, use an 18-mesh sieve to carry out granulation, sieve out the fine powder in the dry granules, mix with the sieved magnesium stearate, and then mix with the dry granules evenly, and press into tablets to obtain the product.
Embodiment 2
[0046] Embodiment 2 Compound pioglitazone bromocriptine tablet
[0047]
[0048] Preparation process: Weigh the prescribed amount of bromocriptine, pioglitazone, microcrystalline cellulose and hydroxypropyl cellulose and mix evenly. Take another appropriate amount of 8% starch slurry solution, add it to the mixed powder, mix evenly to make a soft material, pass through a 16-mesh sieve to granulate, and dry below 60°C. After the drying is completed, use an 18-mesh sieve to carry out granulation, sieve out the fine powder in the dry granules, mix with the sieved magnesium stearate, and then mix with the dry granules evenly, and press into tablets to obtain the product.
Embodiment 3
[0049] Embodiment 3 compound pioglitazone bromocriptine tablet
[0050]
[0051] Preparation process: Weigh the bromocriptine, pioglitazone, starch, dextrin and low-substituted hydroxypropyl cellulose in the prescribed amount and mix them evenly. Another appropriate amount of 60% ethanol is added to the mixed powder, mixed evenly to make a soft material, granulated through a 16-mesh sieve, and dried below 60°C. After the drying is completed, use an 18-mesh sieve to carry out granulation, sieve out the fine powder in the dry granules, mix with the sieved magnesium stearate, and then mix with the dry granules evenly, and press into tablets to obtain the product.
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