A pharmaceutical composition for treating gallbladder-related diseases, preparation method and application thereof
A technology of composition and medicine, which is applied in the field of pharmaceutical composition for treating gallbladder-related diseases, preparation, and herbal medicine composition for treating digestive system diseases. It can solve the problems of patient death, relieve pain, inhibit normal bile secretion, The effect of suppressing excessive secretion of abnormal bile
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Embodiment 1
[0078] The preparation method step of oral liquid of the present invention is as follows:
[0079] Take 4.0-2.0 parts by weight of emblica, 3.2-0.5 parts by weight of myrobalan, and 2.8-0.4 parts by weight of myrobalan. After cleaning, there is no impurity, no moth, no mildew, and it is ready for use after passing the inspection.
[0080] Mix the above components, add 6-20 times the weight of water to decoct twice, each time for 1 hour, filter, combine the filtrate, put it in a vacuum concentration tank, and concentrate under reduced pressure at 60°C and 0.02mpa to a relative density of 1.10- 1. 25 (20°C) extract, add agar and honey, mix evenly, place at 4°C for 48 hours, filter, add appropriate amount of flavoring agent to the filtrate, mix evenly, add appropriate amount of bentonite, mix evenly, place at 4°C for 48 hours, and filter repeatedly , the filtrate is sent to the 100,000 clean level automatic bottling workshop for filling, 30 milliliters per bottle, sterilized, ins...
Embodiment 2
[0100] The steps of the preparation technology of capsule of the present invention are as follows:
[0101] Take 4.0-2.0 parts by weight of emblica, 3.2-0.5 parts by weight of myrobalan, and 2.8-0.4 parts by weight of myrobalan. After cleaning, there is no impurity, no moth, no mildew, and it is ready for use after passing the inspection.
[0102] Mix the above components, add 6-20 times the amount of water to decoct twice, each time for 1 hour, filter, combine the filtrate, put it in a vacuum concentration tank, and concentrate under reduced pressure at 60°C and 0.02mpa to a relative density of 1.10- 1.25 (20°C) extract, add ethanol until the ethanol content reaches 70%, mix well, let it stand overnight, filter, after the filtrate recovers ethanol, put it in a vacuum concentration tank, 60°C, 0.02mpa reduced pressure and concentrate to relative Thick paste with a density of 1.28-1.40 (20°C). Take starch, dextrin, and sugar powder (7:1:1) as auxiliary materials, mix with thic...
Embodiment 3
[0115] Embodiment 3, research on the pharmacological effectiveness of the combination of the present invention
[0116] Experiment 1. The influence of the combination of the present invention on normal bile secretion:
[0117] Guinea pigs were randomly divided into groups according to body weight, 10 in each group. Fasting without food and water for 12 hours before the experiment, the animals in each group were anesthetized with 20% urethane 1mL / 100g.bw intraperitoneally, and then the common bile duct was inserted into the silicone tube for surgery. After the operation was completed, the bile was collected and the volume of bile was measured to observe the stability of bile secretion. The test substance is mainly based on the proposed clinical dose. The equivalent dose converted into guinea pigs based on body surface area is 1.17g crude drug / kg, take 0.52g crude drug / mL SLJ oral liquid, and administer 1mL / 100g, that is, 5.2g crude drug / kg. After the bile secretion was stabl...
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