Medicine for treating climacteric syndrome
A kind of medicine and age-related technology, which is applied in the direction of drug combination, pharmaceutical formula, medical preparations containing active ingredients, etc., can solve the problems that have not been used to treat menopausal syndrome, and achieve clinical effect relief, small side effects, and small stimulating effects Effect
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Embodiment 1
[0036] Process 25 grams of Prasterone Sulfate Sodium (medicinal Prosterosterone Sulfate Sodium, conforming to the 2000 edition of the Chinese Pharmacopoeia, produced by Jiangsu Yangzhou Pharmaceutical Factory) into powder by jet milling and other methods so that the particle size is 20 to 100 microns. Powdered prasterone sulfate sodium and 39 grams of pregelatinized starch (pregelatinized starch, medicinal, Chinese Pharmacopoeia 2000 edition, produced by Huzhou Food and Chemical United Company) and 16 grams of microcrystalline cellulose (microcrystalline cellulose, pharmaceutical Use, Chinese Pharmacopoeia 2000 edition, produced by Shanghai Zhaotun Pharmaceutical Factory) and mix uniformly, add a concentration of 10% (percentage by weight) of starch slurry in an appropriate amount (it is advisable to make the resulting mixture suitable for granulation by conventional methods), mix uniformly , made into a soft material, granulated with a 20-mesh nylon sieve, dried at 50°C for 2 ...
Embodiment 2
[0038] According to the method of Example 1, commercially available Prasterone Sulfate Sodium with common particle size (medicinal Prasterone Sulfate Sodium, conforming to the Chinese Pharmacopoeia 2000 edition, produced by Jiangsu Yangzhou Pharmaceutical Factory) was mixed with other components to prepare pharmaceutical preparation B of the present invention.
Embodiment 3
[0040] Investigate the fluidity of the granules of the preparation A obtained in Example 1, the degree of difficulty of tableting, and the disintegration and dissolution properties after tableting, and the results are listed in the following table. It can be seen from the data in the table that the granules of preparation A have good fluidity, the tablets are formed well, and the disintegration and dissolution rates all meet the requirements.
[0041] Table 1 Quality inspection results after tablet compression
[0042]
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