Isradipine composition medicine, capsule preparation, and preparation method and application of capsule preparation
A technology of isradipine and capsules, which is applied in the field of pharmaceutical composition preparations, can solve the problems of slow effect and long duration, and achieve good active effect
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Embodiment 1
[0012] The investigation of embodiment 1 isradipine combination drug capsule preparation method
[0013] Take the medicinal material according to the weight ratio of isradipine, ferulic acid, calcium sulfate, low-substituted hydroxypropyl cellulose, carboxymethyl cellulose and magnesium stearate in a ratio of 5:2:12:3:2:1, According to different processes, drug test groups were granulated, drug test group 1: purified water; drug test group 2: 50% ethanol; drug test group 3: 5% PVP; drug test group 4: 10% starch paste. All kinds of granules were taken, respectively packed by hard capsule filling machine, and the dissolution rate was checked by an intelligent dissolution apparatus according to the Pharmacopoeia method, and the corresponding dissolution rates of granules with different hardness of each variety were measured, and the results are shown in Table 1.
[0014] Table 1 Effect of different particle hardness on dissolution rate
[0015]
[0016] Take the original powd...
Embodiment 2
[0023] The preparation of embodiment 2 isradipine combination drug capsules
[0024] Take the medicinal materials according to the weight ratio of isradipine, ferulic acid, calcium sulfate, low-substituted hydroxypropyl cellulose, carboxymethyl cellulose and magnesium stearate in a ratio of 5:6:12:3:2:1, Isradipine, ferulic acid, calcium sulfate, low-substituted hydroxypropyl cellulose, carboxymethyl cellulose, and magnesium stearate are wetted with water and granulated, passed through a 100-mesh sieve, and no pressure is applied when the capsules are divided, Obtain drug experiment group I;
[0025] Take the medicinal material according to the weight ratio of isradipine, ferulic acid, calcium sulfate, low-substituted hydroxypropyl cellulose, carboxymethyl cellulose and magnesium stearate in a ratio of 5:2:12:3:2:1, According to the above-mentioned method, the drug experiment group II was obtained;
[0026] Take the medicinal materials according to the weight ratio of isradi...
Embodiment 3
[0027] Example 3 Experimental drug activity investigation on atherosclerosis
[0028] 64 male New Zealand white rabbits, weighing (1.67±0.21) kg. They were randomly divided into 8 groups with 8 animals in each group. The control group received normal pellet feed; the high-fat diet non-intervention group (hereinafter referred to as the non-intervention group) received high-cholesterol feed (1% cholesterol+5% lard pellet feed); the fluvastatin group (hereinafter referred to as the statin group) received high-cholesterol feed. Cholesterol feed + fluvastatin sodium capsule 20 mg, once a day; ferulic acid tablet group received high cholesterol feed + commercially available ferulic acid tablet 35 mg (weight of ferulic acid monomer), once a day; isradipine Tablet group was given high-cholesterol feed+commercially available isradipine tablet 50mg (isradipine monomer weight), once a day; drug experiment group I was given drug experiment group I 30mg (irradipine monomer weight) of high...
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