Phenolphthalein tablets for treating constipation and preparation method thereof
A technology for treating constipation and phenolphthalein, which is applied in the field of medicine to achieve the effect of high efficiency and remarkable curative effect
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Embodiment 1
[0029] Phenolphthalein tablets for treating constipation, which are prepared from the following raw materials:
[0030] 50kg of phenolphthalein, 25kg of starch, 20kg of 10% (by weight) starch slurry, 0.77kg of magnesium stearate, 0.23kg of sodium dodecyl sulfonate
[0031] Get above-mentioned raw material, granulate according to conventional method, prepare 500,000 tablets.
Embodiment 2
[0033] Phenolphthalein tablets for treating constipation, which are prepared from the following raw materials:
[0034] 18kg of phenolphthalein, 25kg of active ingredients of traditional Chinese medicine, 25kg of starch, 22kg of 10% (by weight) starch slurry, 0.77kg of magnesium stearate, 0.23kg of sodium dodecylsulfonate
[0035] Get above-mentioned raw material, granulate according to conventional method, prepare 500,000 tablets.
[0036] The active ingredient of the traditional Chinese medicine is prepared from the raw materials of the following weight:
[0037] 35 parts of cistanche, 35 parts of big belly skin, 35 parts of cassia seed, 35 parts of dandelion, 35 parts of almond,
[0038] 30 parts of privet fruit, 30 parts of mulberry fruit, 30 parts of turmeric, 30 parts of melon, 30 parts of aurantium,
[0039] 25 parts of Artemisia annua, 25 parts of Burdock, 25 parts of Cortex Phellodendri, 25 parts of Baibu, 25 parts of Angelica,
[0040] 20 parts of tangerine peel, 20...
Embodiment 3
[0052] Acute toxicity test: 60 mice, half male and half female, weighing 30-40 g, were used for acute toxicity test. The mice were randomly divided into two groups, i.e. the control group and Example 1 group, Example 2 group, 20 in each group, fasted for 12 hours before the experiment, and the administration group was given the preparation of Example 1 and Example 2 of the present invention respectively. The pharmaceutical composition was dissolved in water for intragastric administration, and the control group was given the same amount of normal saline, administered twice a day, with an interval of 6 hours between administrations. After administration, the mice were continuously observed for two weeks, and the toxic reactions and symptoms of the mice were recorded. deaths. The experimental results showed that: compared with the control group, there was no significant difference in the mice after administration. The experiment was observed for two consecutive weeks, and the ge...
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