Method for extracting tripterygium glycosides, and product and inclusion compound and medicinal composition thereof
A technology of tripterygium glycosides and extraction methods, which is applied in the fields of extraction methods of tripterygium glycosides and the obtained products and their clathrates and pharmaceutical compositions, and can solve the problems of complex components of the extract, high labor intensity, and complicated operations, etc. Achieve the effects of improving bioavailability, reducing energy consumption, and reducing production costs
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Embodiment 1
[0045] Get dry, mildew-free, peeled Tripterygium wilfordii root coarse powder (10kg), mix evenly with 200 mesh chromatography silica gel (15kg) of 1.5 times of weight, pulverize, make it all cross 200 mesh sieves. The homogeneous mixture of the pulverization of Tripterygium wilfordii and adsorbent is packed into a chromatographic column (inner diameter × length is a stainless steel column of 300mm × 1500mm) filled with equal weight chromatographic silica gel (25kg), compacted, and 75kg of medicinal chloroform ( (approximately more than 20cm of solid material) impregnated for 24 hours, and then eluted with chloroform until the eluent was basically colorless, and checked by silica gel G thin plate chromatography, using a mixture of cyclohexane and acetone with a volume ratio of 5:3 as the developer , after unfolding and drying, after confirming that the blue fluorescent spots at the front extension have disappeared, elute with a chloroform solution containing 5% ethanol mass perc...
Embodiment 2
[0047] Get dry, mildew-free, peeled tripterygium root coarse powder (10kg), mix evenly with 1.5 times the weight of chromatographic silica gel (15kg), pulverize, and make it all pass through a 200-mesh sieve. The pulverized homogeneous mixture of Tripterygium wilfordii and adsorbent is packed into a chromatographic column (300 × 1500mm stainless steel column) filled with equal weight chromatographic silica gel (25kg), compacted, and 75kg of medicinal chloroform (about 20cm above the solid material) is added. ) for 24 hours, and then eluted with chloroform until the eluent is basically colorless, checked by silica gel G thin plate chromatography, using a mixture of cyclohexane and acetone with a volume ratio of 5:3 as the developer, and dried in the air after development. After confirming the disappearance of the blue fluorescent spots at the front extension, elute with a chloroform solution containing 5% ethanol by mass until the eluate is colorless, and collect and combine the...
Embodiment 3
[0050] Take by weighing the Tripterygium wilfordii polyglycoside 50g of embodiment 1 gained, and auxiliary material starch 98.2g, dextrin 5g, calcium hydrogen phosphate 250g, low-substituted hydroxypropyl cellulose 40g, get the starch of 13.2g and make 8% starch slurry altogether 165g, Mix with other substances, shake and granulate with 18 mesh, put it in an oven, dry at 60°C, granulate through 18 mesh, then add 4.4g of magnesium stearate, mix for 10 minutes, and calculate as each tablet contains 10mg tripterygium glycosides Tablet weight, with a 5.5mm round shallow punched tablet. The average tablet weight is 0.088-0.089g / tablet, and the content of triptolide A is 0.82mg / g.
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