Preparation method and application of ginseng fruit medicinal dispersing tablets and buccal tablets
A technology of dispersible tablets and ginseng fruit, which is applied to diseases with deficiency of heart and spleen, and treats the field of deficiency of qi and yin, and achieves the effect of high bioavailability and fast absorption.
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Embodiment 1
[0046] The extraction and preparation process of the medicine of the present invention is as follows: (1) Break 5 kg of dried ginseng fruit into tiny blocks, add 8 times the amount of water to decoct 3 times, each time for 1.5 hours, filter, and combine the filtrates. (2) Clear paste concentrated to a relative density of 1.05 (60°C). (3) Add 40% and 70% ethanol in sequence, let stand at 5°C for 12 hours, filter, and combine the filtrate; recover the alcohol from the filtrate and dilute it with water to a clear paste with a relative density of 1.35 (60°C), dry, and ultrafinely pulverize , to obtain about 650g of the main ingredient superfine powder. (4) Precisely weigh 100g of the main superfine powder, add appropriate amount of auxiliary materials, mix well, and make dispersible tablets / lozenges.
[0047] Wherein, the adjuvants adopted in the dispersible tablet are respectively calcium sulfate 30g, cross-linked polyvinylpyrrolidone 4g, 10% polyvinylpyrrolidone K30 aqueous sol...
Embodiment 2
[0049] The extraction and preparation process of the medicine of the present invention is as follows: (1) Break 5 kg of dried ginseng fruit into tiny blocks, add 8 times the amount of water to decoct 3 times, each time for 1.5 hours, filter, and combine the filtrates. (2) Clear paste concentrated to a relative density of 1.10 (60°C). (3) Add 50% and 70% ethanol in turn, let stand at 8°C for 24 hours, filter, and combine the filtrate; recover the alcohol from the filtrate and dilute with water to a clear paste with a relative density of 1.36 (60°C), dry, and ultrafinely pulverize , to obtain the main drug superfine powder. (4) Add appropriate amount of auxiliary materials, mix well, and make dispersible tablets / lozenges, that is, ready.
[0050] Wherein, the adjuvants adopted in the dispersible tablet are respectively calcium sulfate 40%, cross-linked polyvinylpyrrolidone 6%, 10% polyvinylpyrrolidone K30 aqueous solution 4%, Tween- 80 0.4%, micropowder silica gel 4%; the adju...
Embodiment 3
[0052] The extraction and preparation process of the medicine of the present invention is as follows: (1) Break 5 kg of dried ginseng fruit into tiny blocks, add 8 times the amount of water to decoct 3 times, each time for 1.5 hours, filter, and combine the filtrates. (2) Clear paste concentrated to a relative density of 1.15 (60°C). (3) Add 60% and 70% ethanol in sequence, let stand at 10°C for 48 hours, filter, and combine the filtrate; recover the alcohol from the filtrate and dilute it with water to a clear paste with a relative density of 1.37 (60°C), dry, and ultrafinely pulverize , to obtain the main drug superfine powder. (4) Add appropriate amount of auxiliary materials, mix well, and make dispersible tablets / lozenges, that is, ready.
[0053] Wherein, the adjuvants adopted in the dispersible tablet are respectively calcium sulfate 50%, cross-linked polyvinylpyrrolidone 8%, 10% polyvinylpyrrolidone K30 aqueous solution 6%, Tween- 80 0.6%, micronized silica gel 6%; t...
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