Preparation method of medicine for treating hypertension
A technology for treating drugs and hypertension, which is applied in the field of preparing drugs for treating hypertension, can solve problems such as adverse reactions, instability of sustained-release system, etc., and achieves increasing compatibility, maintaining effective blood drug concentration, and increasing storage stability. Effect
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Embodiment 1
[0021] First, mix shell powder, organic microspheres, and polyvinyl alcohol with a mass ratio of 100:5:1 to make a green body; then remove organic matter by sintering at 900°C to form micropores, and ball mill it into powder to obtain a support material; weigh 0.2g Hydrochlorothiazide, 9.3g carbonate polymer, mixed uniformly according to the method of equal addition, then added 0.3g support material and 0.2g hydroxypropylcellulose propylene glycol solution with a mass concentration of 12%, granulated with a 30-mesh sieve, and dried at 60°C for 4h , after being sized through a 24-mesh sieve, mixed evenly, and compressed into tablets to obtain the drug.
Embodiment 2
[0023] First, mix shell powder, organic microspheres, and polyvinyl alcohol with a mass ratio of 100:4:1 to make a green body; then remove organic matter by sintering at 850°C to form micropores, and ball mill into powder to obtain a support material; weigh 0.3g Losartan, 9g carbonate polymer, mixed uniformly according to the method of equal addition, then add 0.6g support material and 0.1g mass concentration of 12% hydroxypropyl cellulose propylene glycol solution, granulate with 30 mesh sieve, dry at 60°C After 4 hours, 24-mesh sieve sieves the granules, mixes them evenly, and compresses them into tablets to complete.
Embodiment 3
[0025] First, mix shell powder, organic microspheres, and polyvinyl alcohol with a mass ratio of 100:4.5:1 to make a green body; then remove organic matter by sintering at 900°C to form micropores, and ball mill into powder to obtain a support material; weigh 0.3g Losartan, 9g carbonate polymer, mixed uniformly according to the method of equal addition, then add 0.6g support material and 0.1g mass concentration of 12% hydroxypropyl cellulose propylene glycol solution, granulate with 30 mesh sieve, dry at 60°C After 4 hours, 24-mesh sieve sieves the granules, mixes them evenly, and compresses them into tablets to complete.
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