Pharmaceutical compound preparation and application of pharmaceutical compound preparation in preparing medicines for treating hypertension with coronary heart disease
A compound preparation and drug technology, applied in the field of medicine, can solve the problems of poor patient compliance, high cost of long-term medication, and a wide variety of medication, and achieve significant curative effects.
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Embodiment 1
[0020] Formula composition:
[0021] 15 parts by weight of lovastatin
[0022] 15 parts by weight of bumetanide
[0023] 20 parts by weight of metolazone
[0024] 10 parts by weight of citric acid
[0025] 10 parts by weight of butylated hydroxyanisole
[0026] 40 parts by weight of lactose
[0027] 25 parts by weight of hydroxypropyl cellulose
[0028] 20 parts by weight of sodium carboxymethyl starch
[0029] 10 parts by weight of micronized silica gel
[0030] Preparation:
[0031] 1) Take prescription amounts of lovastatin, bumetanide, and metolazone, add citric acid, butylated hydroxyanisole, and lactose to mix well, and set aside.
[0032] 2) Add hydroxypropyl cellulose, cross-linked polyvinylpyrrolidone and sodium carboxymethyl starch to 1) and mix thoroughly, pass 80 mesh sieve, ethanol made soft material, pass 14 mesh sieve for granulation.
[0033] 3) Dry, granulate, add micro-powdered silica gel and mix well, then press into tablets, ready to be obtained.
Embodiment 2
[0035] Formula composition:
[0036] Lovastatin 20 parts by weight
[0037] Bumetanide 20 parts by weight
[0038] 35 parts by weight of metolazone
[0039] 20 parts by weight of citric acid
[0040] 20 parts by weight of butylated hydroxyanisole
[0041] 50 parts by weight of lactose
[0042] 30 parts by weight of hydroxypropyl cellulose
[0043] 30 parts by weight of sodium carboxymethyl starch
[0044] 15 parts by weight of micronized silica gel
[0045] Preparation:
[0046] 1) Take prescription amounts of lovastatin, bumetanide, and metolazone, add citric acid, butylated hydroxyanisole, and lactose to mix well, and set aside.
[0047] 2) Add hydroxypropyl cellulose, cross-linked polyvinylpyrrolidone and sodium carboxymethyl starch to 1) and mix thoroughly, pass 80 mesh sieve, ethanol made soft material, pass 14 mesh sieve for granulation.
[0048] 3) Dry, granulate, add micro-powdered silica gel and mix well, then press into tablets, ready to be obtained.
Embodiment 3
[0050] Formula composition:
[0051] 5 parts by weight of lovastatin
[0052] 10 parts by weight of bumetanide
[0053] 10 parts by weight of metolazone
[0054] 5 parts by weight of citric acid
[0055] 5 parts by weight of butylated hydroxyanisole
[0056] 25 parts by weight of lactose
[0057] 15 parts by weight of hydroxypropyl cellulose
[0058] 10 parts by weight of sodium carboxymethyl starch
[0059] 2 parts by weight of micronized silica gel
[0060] Preparation
[0061] 1) Take prescription amounts of lovastatin, bumetanide, and metolazone, add citric acid, butylated hydroxyanisole, and lactose to mix well, and set aside.
[0062] 2) Add hydroxypropyl cellulose, cross-linked polyvinylpyrrolidone and sodium carboxymethyl starch to 1) and mix thoroughly, pass 80 mesh sieve, ethanol made soft material, pass 14 mesh sieve for granulation.
[0063] 3) Dry, granulate, add micro-powdered silica gel and mix well, then press into tablets, ready to be obtained.
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