Yuanhuzhitong granule and preparation method thereof
A Yuanhu analgesic and granule technology, which is applied in the direction of non-central analgesics, pharmaceutical formulas, medical preparations with non-active ingredients, etc., can solve problems such as poor stability and slow drug onset
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Embodiment 1
[0014] Example 1 Preparation of Yuanhu Zhitong Granules
[0015] Take 200g of Angelica dahurica and grind it into fine powder, pass through a 100-mesh sieve; crush 1800g of Angelica dahurica and 4000g of vinegar corydalis and sieve into coarse powder, soak with 6 times the amount of 60% ethanol for 14 hours, heat and reflux for 3 hours, and collect the extract; then Add 8 times the amount of 70% ethanol and heat to reflux for 3 hours, collect the extract, combine the two extracts, filter, and concentrate the filtrate to obtain a thick paste; then add the prepared fine powder of Angelica dahurica, mix well, dry in vacuum, and pulverize Pass through a 80-mesh sieve; add 9g of ethyl cellulose, 13g of mannitol and 18g of sucrose to the dried medicinal powder; use 70% ethanol as a soft material, granulate with a 16-mesh sieve, and dry and fill it (5g per bag).
Embodiment 2
[0016] Example 2 Investigation of the performance of Yuanhu Zhitong Granules
[0017] (1) Measurement of angle of repose
[0018] The fixed funnel method was used to measure the angle of repose. Three funnels were connected in series and fixed at a height of 1 cm on the horizontal coordinate paper, and the Chinese medicine particles were poured into the top funnel along the funnel wall until the tip of the cone of particles formed on the coordinate paper touched the funnel. The diameter of the cone bottom is measured from the coordinate paper, and the angle of repose is calculated. The specific results are as follows:
[0019]
Embodiment 3
[0027] Example 3 Investigation on the Stability of Yuanhuzhitong Granules
[0028] The stability of the relevant granules was investigated in accordance with the guidelines on stability in the fourth part of the Chinese Pharmacopoeia 2015 edition, and the stability of the drug was investigated at 25°C for 36 months, at 45°C and at a relative humidity of 75% for 60 days. According to the Chinese Pharmacopoeia 2015 edition one about the quality inspection method of Yuanhu Zhitong Granules, the content of imperatorin and tetrahydropalmatine in the granules was determined by HPLC method.
[0029] Content of active ingredients in granules after storage at 25°C for 36 months
[0030]
[0031] Stored at 45°C and 75% relative humidity for 60 days
[0032]
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