Tablet used for treating prostate diseases as well as preparation method and application thereof
A prostate and tablet technology, which is applied in the field of tablet preparation for the treatment of prostate diseases, can solve the problems of difficult to meet the quality standards of pharmaceutical tablets, the shelf life of pharmaceuticals, and unqualified pharmaceutical quality, and achieve moderate hardness and friability. character, the amount of excipients and the effect of small quantity
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Embodiment 1
[0021] Example 1 : the preparation method of tablet of the present invention
[0022] The present embodiment is the preparation method of tablet of the present invention, specifically comprises the following steps:
[0023] (1) Take 250 kg of bristle grass and 125 kg of saponins, add 1800 L of water, heat and reflux for extraction for 2 hours, and concentrate the extract to a relative density of 1.20-1.25 (80°C).
[0024] (2) 25 kg of Wang Buliuxing were stir-fried and processed at a temperature of 160-170°C for 5-6 minutes, crushed and passed through a 40-mesh sieve.
[0025] (3) Mix the fine powder of wangbuliuxing with the above-mentioned extract prepared from bristle grass and saponaria thorn, vacuum dry and pulverize, and pass through a 40-mesh sieve to obtain extract powder.
[0026] (4) Processing of mole crickets: Heat the pot with a slow fire, sprinkle 3.75 kg of bran with a mesh size greater than 20, stir fry continuously to generate smoke, add 15 kg of mole cricke...
Embodiment 2
[0031] Example 2 : identification of tablet of the present invention
[0032] Respectively according to the Chinese Pharmacopoeia 2005 Edition 1 Appendix XIIA "Disintegration Time Limit Inspection Method", Chinese Pharmacopoeia 2005 Edition 2 Edition Appendix XG "Tablet Friability Inspection Method", and Chinese Pharmacopoeia 2005 2 Edition Appendix XIXC "Drug Preparation Stability Test Guidelines", the disintegration, friability, and stability of the tablet prepared in the above-mentioned embodiment 1 are tested and investigated, and compared with the tablet made by conventional technology (according to Chinese patent CN1235608C Prepared by the method disclosed in) is carried out comparative test as a contrast, and in fact the results are as follows:
[0033] 1) Disintegration time limit test of tablets
[0034]The test is divided into three groups, and each group takes 6 tablets made by the technology of the present invention. According to the Chinese Pharmacopoeia in 200...
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