Leucogen oral disintegration tablet and its preparing method
An orally disintegrating tablet and blood-reducing technology, which is applied in the fields of blood diseases, pill delivery, extracellular fluid diseases, etc., can solve the problems of slow dissolution of oral dosage forms, low bioavailability, and difficulty in swallowing, and achieves no unpleasant taste, High bioavailability, enhanced function
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Embodiment 1
[0033] Embodiment 1: prescription test
[0034] Lexogen 10.0g
[0035] Lactose 34.0g
[0036] Mannitol 20.0g
[0037] Microcrystalline Cellulose 26.0g
[0038] Low-substituted hydroxypropyl cellulose 2.5g
[0039] Cross-linked polyvinylpyrrolidone 2.5g
[0040] Magnesium Stearate 1.0g
[0041] Sodium bicarbonate 1.0g
[0042] Citric acid 1.0g
[0043] Aspartame 1.0g
[0044] Peppermint essence 1.0g
[0045] A total of 1000 tablets were produced
[0046] Preparation method: Take the above-mentioned components, pulverize them, pass through a 100-mesh sieve, weigh each component according to the above-mentioned prescription amount, mix them uniformly, send the powder into a conventional tablet machine, and perform tablet compression to obtain a tablet with a weight of 100 mg. Xuesheng orally disintegrating tablets.
[0047] Test result: Tablet hardness: 15~40N
[0048] Disintegration time limit: 20-50 seconds
[0049] Taste: No gritty and unpleasant taste, ...
Embodiment 2
[0050] Embodiment 2: prescription test
[0051] Lexogen 20.0g
[0052] Mannitol 60.0g
[0053] Sorbitol 33.0g
[0054] Microcrystalline Cellulose 47.0g
[0055] Low-substituted hydroxypropyl cellulose 10.0g
[0056] Cross-linked polyvinylpyrrolidone 20.0g
[0057] Magnesium Stearate 2.0g
[0058] Sodium bicarbonate 2.0g
[0059] Citric acid 2.0g
[0060] Sucralose 2.0g
[0061]Peppermint essence 2.0g
[0062] A total of 1000 tablets were produced
[0063] Preparation:
[0064] Step 1: Grind the leucogen and various auxiliary materials separately, pass through a 100-mesh sieve, and store them separately for later use;
[0065] Step 2: Weigh Lexusan, mannitol, and 75% of the prescribed amount of microcrystalline cellulose, low-substituted hydroxypropyl cellulose, and cross-linked polyvinylpyrrolidone according to the prescribed amount, and fully mix them;
[0066] Step 3: Add an appropriate amount of absolute ethanol to the above-mentioned uniformly mixed components,...
Embodiment 3
[0072] Embodiment 3: prescription test
[0073] Lexogen 10.0g
[0074] Mannitol 70.0g
[0075] Sorbitol 33.0g
[0076] Microcrystalline Cellulose 47.0g
[0077] Low-substituted hydroxypropyl cellulose 10.0g
[0078] Cross-linked polyvinylpyrrolidone 20.0g
[0079] Magnesium Stearate 2.0g
[0080] Sodium bicarbonate 2.0g
[0081] Citric acid 2.0g
[0082] Sucralose 2.0g
[0083] Peppermint essence 2.0g
[0084] A total of 1000 tablets were produced
[0085] Preparation method: Weigh each component according to the above prescription amount, mix them evenly, pass through a 100-mesh sieve, send the powder into a conventional tablet press, and perform tablet compression to obtain Lixuesheng orally disintegrating tablets with a tablet weight of 200 mg.
[0086] Test result: Tablet hardness: 15~40N
[0087] Disintegration time limit: 20-50 seconds
[0088] Taste: No gritty and unpleasant taste, no foreign body feeling.
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