Aspirin slow-release tablet and its prepn. method
A technology of aspirin and sustained-release tablets, applied in the field of human medicine, can solve the problems of seldom application, large dose, gastrointestinal bleeding, etc., and achieve the effects of improving compliance, improving absorption rate, and prolonging action time.
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Embodiment 1
[0075] Aspirin sustained-release tablets, its composition includes: aspirin, starch, hypromellose, polyacrylic resin No. II, white dextrin, talc, tartaric acid, Tween-80, 75% ethanol, the above The weight ratio of the ingredients is 50 aspirin, starch 1, hypromellose 2.48, polyacrylic resin II 3.6, white dextrin 1, talc 3, tartaric acid 0.21, Tween-80 is 0.15, 75 % Ethanol 12.
[0076] Administration method and dosage, 50-150mg (1-3 tablets) each time orally, once a day or as directed by a doctor.
Embodiment 2
[0078] The above-mentioned preparation process of aspirin sustained-release tablets takes hypromellose 0.48, polyacrylic resin II 0.6, tartaric acid 0.21, Tween-80 0.15, and 75% ethanol 12 to prepare a solution for bonding. Add aspirin 50, starch 1, hypromellose 2, polyacrylic resin No. 2 3, white dextrin 1, put in a mixer for 10 minutes, and then add the prepared adhesive It is wet mixed for 100 seconds to make a soft material, granulated by a 20-mesh screen, dried by a boiling dryer, and controlled the inlet air temperature not to be higher than 100°C. Add talc powder 3 to the dry granule, and granulate with an 18-mesh screen. The prepared granules are compressed with a press to obtain aspirin sustained-release tablets.
Embodiment 3
[0080] For the bioavailability experiment of aspirin sustained-release tablets, the single-dose subjects were randomly divided into two groups (A, B), and carried out according to the crossover test. Group A was self-made sustained-release tablets, and group B was enteric-coated tablets. Each medication was taken one week apart. The subjects were taken blood on an empty stomach in the morning, followed by taking the medication. The blood was taken with 150ml of warm water. The blood collection time was 0, 1, 1.5, 2, 3, 4, 5, 6, 8, 10, 12, 24. After hours, venous blood was taken, after processing, the plasma was taken, stored at low temperature, and determined by HPLC method.
[0081] Drug source: experimental drugs, aspirin sustained-release tablets each containing 50mg of the main drug, the actual content is 101.20%. The reference substance, aspirin enteric-coated tablets (25mg / tablet), the actual content is 100.86%, produced by Jinan No. 3 Pharmaceutical Factory.
[0082] Dosage...
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