Prunella vulgaris extract dispersible tablets and preparation method and use thereof
A technology of Prunella vulgaris and its extract, which is applied in the field of traditional Chinese medicine pharmaceutical preparations, can solve the problems of slow disintegration and dissolution of drugs, reduced drug bioavailability, poor stability and the like
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Embodiment 1
[0010] Embodiment 1, take the coarse powder of Prunella vulgaris medicinal material, extract 3 times with 95% ethanol of 8 times the amount of medicinal material, 2 hours each time, filter, combine the alcohol extract, concentrate to obtain extract, degrease with petroleum ether, filter, The obtained solid was dried in an oven at 50°C for 2 hours to obtain the ethanol extract of Prunella vulgaris, which was pulverized and passed through a 120-mesh sieve for later use.
[0011] Take 25 parts of the above-mentioned Prunella vulgaris ethanol extract, 40 parts of microcrystalline cellulose, 20 parts of lactose, 4 parts of cross-linked polyvinylpyrrolidine and 2.5 parts of sodium carboxymethyl starch, and mix them uniformly; 95% ethanol is used as a wetting agent in an appropriate amount. Granulate and dry; add 4 parts of cross-linked polyvinylpyrrolidone, 2.5 parts of sodium carboxymethyl starch, 1 part of micropowdered silica gel and 1 part of magnesium stearate to the dry granule...
Embodiment 2
[0012] Example 2: Take 20 parts of Prunella vulgaris alcohol extract in Example 1, 20 parts of microcrystalline cellulose, 30 parts of lactose, 2.5 parts of cross-linked polyvinylpyrrolidine and 3 parts of sodium carboxymethyl starch, and mix evenly; 95% Appropriate amount of ethanol is used as wetting agent, granulated, and dried; add 2.5 parts of cross-linked polyvinylpyrrolidone, 3 parts of sodium carboxymethyl starch, and 1 part of micropowdered silica gel 10.5 magnesium stearate to the dry granules, granulate, and compress into tablets to obtain Dispersible tablet preparation.
Embodiment 3
[0013] Example 3: Take 25 parts of Prunella vulgaris ethanol extract, 40 parts of microcrystalline cellulose, 30 parts of lactose, 2 parts of cross-linked polyvinylpyrrolidine and 4 parts of sodium carboxymethyl starch in Example 1, and mix evenly; 95% Appropriate amount of ethanol is used as wetting agent, granulated, and dried; 2 parts of cross-linked polyvinylpyrrolidone, 3.5 parts of sodium carboxymethyl starch, 1 part of micropowder silica gel and 0.5 part of magnesium stearate are added to the dry granules, and the whole granules are compressed into tablets. That is, a dispersible tablet preparation is obtained.
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