Application of puerarin or medicinal composition containing puerarin in preparation of medicament with effect of preventing or treating senile dementia
A technology for senile dementia and puerarin, applied in the direction of drug combinations, medical preparations containing active ingredients, active ingredients of heterocyclic compounds, etc., can solve the problem of unclear application of Pueraria total flavonoids composition, prone to severe adverse reactions, Problems that do not meet the principles of medication, etc., to achieve the effect of improving motor function and therapeutic effect, improving cognitive ability and quality of life, and complementing the mechanism of drug action
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Embodiment 1
[0027] Example 1 Preparation of Puerarin Tablets
[0028] Puerarin 0.1g
[0029] Starch 25g
[0030] Dextrin 35g
[0031] Low-substituted hydroxypropyl cellulose 5g
[0032] 60% ethanol appropriate amount
[0034] Preparation process: Weigh the prescribed amount of puerarin, starch, dextrin and low-substituted hydroxypropyl cellulose and mix evenly. Another appropriate amount of 60% (volume percentage, the same below) ethanol is added to the mixed powder, mixed evenly to make a soft material, granulated through a 16-mesh sieve, and dried below 60°C. After drying, use an 18-mesh sieve to carry out granulation, sieve out the fine powder in the dry granules, mix with the sieved magnesium stearate, and then mix with the dry granules evenly, and press into tablets to obtain the product. The content of puerarin in each preparation unit is 0.1 mg-200 mg, and the dosage for human use is 0.1 mg / kg·d~5 mg / kg·d.
Embodiment 2
[0035] Example 2 Preparation of Puerarin Tablets
[0036] Puerarin 25g
[0037] Microcrystalline Cellulose 180g
[0038] Hydroxypropyl Cellulose 15g
[0039] 8% (mass percentage content) starch slurry appropriate amount
[0040] Magnesium Stearate 1.5g
[0041] Preparation process: Weigh the prescribed amount of puerarin, microcrystalline cellulose and hydroxypropyl cellulose and mix evenly. Take another appropriate amount of 8% starch slurry solution, add it to the mixed powder, mix evenly to make soft material, pass through a 16-mesh sieve to granulate, and dry below 60°C. After drying, use an 18-mesh sieve to carry out granulation, sieve out the fine powder in the dry granules, mix with the sieved magnesium stearate, and then mix with the dry granules evenly, and press into tablets to obtain the product.
[0042] The content of puerarin in each preparation unit is 0.1mg~200mg, and the dosage for human use is 0.1mg / kg·d~5mg / kg·d.
Embodiment 3
[0043] Example 3 Preparation of Puerarin Tablets
[0044] Puerarin 25g
[0045] Triptolide 2.5g
[0046] Starch 25g
[0047] Dextrin 35g
[0048] Low-substituted hydroxypropyl cellulose 5g
[0049] 60% ethanol appropriate amount
[0051] Preparation process: Weigh the prescription amount, puerarin, triptolide starch, dextrin and low-substituted hydroxypropyl cellulose and mix evenly. Take another appropriate amount of 60% ethanol, add it to the mixed powder, mix it evenly to make a soft material, granulate it through a 16-mesh sieve, and dry it below 60°C. After drying, use an 18-mesh sieve to carry out granulation, sieve out the fine powder in the dry granules, mix with the sieved magnesium stearate, and then mix with the dry granules evenly, and press into tablets to obtain the product. The content of puerarin in each preparation unit is 0.1 mg-200 mg, and the dosage for human use is 0.1 mg / kg·d~5 mg / kg·d.
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