Optimizing method for attenuation processing of Tripterygium wilfordii and related formulation
An optimization method, the technology of Tripterygium wilfordii, which is applied in the field of purification and identification, and extraction of natural medicines, can solve difficult problems and achieve the effects of simple operation, reduced toxicity and significant efficacy
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Embodiment 1
[0021] Weigh 200g of Tripterygium wilfordii, soak it in concentrated hydrochloric acid, and place it in a -20°C refrigerator for 5 minutes. After taking it out, extract it with chloroform three times, 300ml each time, wash the extract with water until it is neutral, and then wash it with anhydrous Na 2 SO 4 After drying and concentrating under reduced pressure, 5.68 g of a concentrate was obtained to prepare a preparation. Add 20mL of water to dissolve, filter and add 2g of potassium sorbate to prepare decoction or mixture; or add hypromellose (HPMC) and mix well, dissolve citric acid in ethanol as wetting agent to make soft material, granulate and dry , whole grains, mixed with magnesium stearate, and pressed into tablets; or dried, ground and passed through a 400-mesh sieve, mixed with 10 mg of sucrose 40 mg, added 0.8 mg of stearic acid, filled into No. 5 empty capsules and sealed to prepare capsules agent; or add water, add simple syrup, add glycerin to aid dissolution, ...
Embodiment 2
[0023] Weigh 200 g of Tripterygium wilfordii, soak it in a hydrochloric acid solution with a pH of 6.0, and place it in a refrigerator at 4°C for 48 hours. After taking it out, extract it with chloroform three times, 300ml each time, wash the extract with water until it is neutral, and then wash it with anhydrous Na 2 SO 4 After drying and concentrating under reduced pressure, 5.37 g of a concentrate was obtained to prepare a preparation. The relevant preparation method is the same as in Example 1.
Embodiment 3
[0025] Weigh 200 g of Tripterygium wilfordii, soak it in a hydrochloric acid solution with a pH of 6.0, and place it at 50° C. for 48 hours. After taking it out, extract it with chloroform three times, 300ml each time, wash the extract with water until it is neutral, and then wash it with anhydrous Na 2 SO 4 After drying and concentrating under reduced pressure, 5.62 g of a concentrate was obtained to prepare a preparation. The relevant preparation method is the same as in Example 1.
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