Medicament for curing dysuria, preparation method and quality control method thereof
A quality control method and drug technology, applied in the direction of drug combinations, pharmaceutical formulations, medical preparations containing active ingredients, etc., can solve problems such as poor controllability, unreasonable quality control methods, and affect the stability of curative effect, etc., to achieve technological controllable effect
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Embodiment 1
[0155] Embodiment 1, common tablet of the present invention
[0156] 300 parts of psoralen and 480 parts of motherwort
[0157] 300 servings of Haijinsha, 240 servings of Shanzi Mushroom
[0158] Weigh the above medicinal materials, among which sea ginseng is fried, add 8 times the amount of water each time and steam it twice, the first time is 3 hours, and the second time is 1 hour. Combine the decoctions, filter, and concentrate the filtrate under reduced pressure to a clear paste with a relative density of about 1.35 (measured at 60°C), and vacuum-dry (60°C) to obtain a dry paste. Crush, sieve (through 80 mesh sieve), add appropriate amount of starch, mix well, granulate with 80% ethanol (18 mesh sieve), dry (60°C), granulate (18 mesh sieve), add appropriate amount of microcrystalline Cellulose and 0.1% magnesium stearate, compressed into 1000 tablets, that is.
Embodiment 2
[0159] Embodiment 2, sugar-coated tablet of the present invention
[0160] 300 parts of psoralen, 480 parts of motherwort, 300 parts of desmodium
[0161] 300 parts of Haijinsha, 30 parts of amber, 240 parts of Shanzi mushroom
[0162] Weigh the six herbs, crush the amber into fine powder, pass through an 80-mesh sieve, and set aside; the rest of the five flavors such as psoralen, among which sea ginseng is fried, add 8 times the amount of water each time and cook twice, the first time for 3 hours, The second time is 1 hour; the decoction is combined, filtered, and the filtrate is concentrated under reduced pressure to a clear paste with a relative density of about 1.35 (measured at 60° C.), vacuum dried (60° C.) to obtain a dry paste. Pulverize, sieve (through 80 mesh sieve), add the amber fine powder and appropriate amount of starch, mix well, granulate (18 mesh sieve) with 80% ethanol, dry (60°C), granulate (18 mesh sieve) , add an appropriate amount of microcrystalline c...
Embodiment 3-7
[0164] The kind of medicinal material of embodiment 3-5 and preparation are the same as embodiment 1, the kind of medicinal material of embodiment 6-7 and preparation are the same as embodiment 2
[0165] Table 10 Examples 3-7
[0166]
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