Bulk medicament for treating orthopedic disorders and preparation method thereof
A technology for orthopedic diseases and raw materials, applied in bone diseases, medical formulas, plant raw materials, etc., can solve the problem of the preparation method of high-purity Dipsacus saponin VI reported, and the application of high-purity Dipsacosa saponin VI in orthopedic diseases Reporting and other issues
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Embodiment 1
[0046] Take 1 kg of Dipsacus, extract twice with 8L 70% ethanol, reflux for 2 hours each time, combine the extracts, concentrate under reduced pressure, recover the ethanol until there is no alcohol smell, add water to dilute to a liquid containing 1.0g of medicinal materials per ml, and use 5% Adjust the pH of the calcium hydroxide suspension to 8-9, let it stand for 12 hours, take the supernatant, and filter to obtain the filtrate. Add the filtrate to the chromatographic column of 1.0kg SA-2 macroporous resin, and after cyclic adsorption twice, use 3L of 1.0% KOH to elute, then wash with water until nearly neutral, then use 3L of 30% ethanol to elute, before discarding Two eluents; finally washed with 7L of 60% ethanol, collected eluate, decolorized with 0.5% activated carbon, filtered, recovered ethanol under reduced pressure, concentrated and dried to obtain 80.9 grams of light yellow Dipsacus saponin VI crude product.
[0047] Add water to the crude product of Dipsacus sa...
Embodiment 2
[0049] Take 1 kg of Dipsacus, crush it, soak it in 6L of water-saturated n-butanol overnight, then start percolating, collect n-butanol, extract it with an equal volume of n-butanol saturated water for 3 times, recover n-butanol under reduced pressure until it is nearly dry, add water Dilute to a liquid containing 0.8g medicinal material per milliliter, let it stand for 12 hours, filter, take the filtrate, add the filtrate to the chromatographic column of 1.5kg ADS-5 macroporous resin, circulate and adsorb for 3 times, wash with 3L of 0.5% NaOH Then wash with water until it is nearly neutral, then use 3L of 30% ethanol to elute, discard the first two eluents, and finally wash with 5L of 70% ethanol, collect the 70% ethanol eluate, and decolorize it with D208 decolorizing resin. The ethanol was recovered under reduced pressure, concentrated and dried to obtain 52.6 g of crude product of light yellow Dipsacus saponin VI.
[0050] Soak 200g of reverse-phase column ODS packing mat...
Embodiment 3
[0052] Take 1 kg of Dipsacus, crush it, moisten it with 1 times the amount of 80% ethanol, soak it in 6L of 80% ethanol for 15 hours, and then start percolation, 5ml / min, collect the percolation liquid, concentrate under reduced pressure, and recover the ethanol until it has no alcohol smell Finally, add water to 3000ml, let it stand for 4 hours, filter, take the filtrate, add the filtrate to the chromatographic column of 1.2kg ADS-8 macroporous resin, after circulating and adsorbing for 3 times, elute with 4L of water, and then use 4L of 30 % ethanol for elution, discard the eluent, discard the first two eluents, then rinse with 4L 90% ethanol, collect the 90% ethanol eluate, and decolorize the 90% ethanol eluate per acidic alumina column (6.0 cm × 8.0cm), ethanol was recovered under reduced pressure, concentrated, and vacuum-dried to obtain 51.3 grams of crude product of Dipsacus saponin VI in light yellow color.
[0053] Take 8 g of the crude product of Dipsacus saponin VI ...
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