Method for extracting ganglioside from animal tissue
A ganglioside, animal tissue technology, applied in chemical instruments and methods, sugar derivatives, sugar derivatives and other directions, can solve the problems of high cholesterol content, high production cost, poor product purity, etc., and achieves simple production process, Yield and purity improvement, the effect of saving extraction time
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Embodiment 1
[0034] Grind 100 grams of pig brain tissue with a meat grinder, homogenate, soak three times in acetone in a cold place, use 3 times the amount for the first time, 2.5 times the amount for the second time, and 1.5 times the amount for the third time, each time 24 hours, filter with muslin or filter press;
[0035] Add 200ml of water and 1200ml of tetrahydrofuran to the above-mentioned processed pig brain tissue, stir well, centrifuge, and repeat the extraction once with 300ml of tetrahydrofuran for the residue, combine the secondary extracts, add 450ml of petroleum ether, perform multi-component distribution, and obtain the lower layer after layering. The polar solvent phase, the upper non-polar solvent phase was repeatedly extracted with 100ml of water, the lower polar solvent phase was combined, filtered, concentrated under reduced pressure at 45°C, and freeze-dried to obtain the finished product, which was grayish white, soluble in water, and soluble in chloroform— -Methano...
Embodiment 2
[0037] Grind and homogenate 500 grams of porcine brain tissue, dry it with hot air at 60°C, and grind it into a fine powder (moisture is less than 8%). Take the above-mentioned brain dry powder, soak it in acetone for 5 hours, repeat 5 times, filter, and put it on the filter cake Add 80% ethanol aqueous solution in the ratio of 1:5, stir fully for 1.5 hours, then add n-hexane according to 1:4, stir fully for 1.5 hours, after static layering, separate the ethanol solution in the lower layer, and use the upper non-polar phase Repeat extraction with 500ml of water, combine the alcohol and water extracts, concentrate under reduced pressure at 40°C, and freeze-dry to obtain the finished product, which is white or off-white with a purity of 79.0%.
Embodiment 3
[0039] 1 kg of bovine placenta, minced, homogenized, treated with acetone by the method of Example 1, added 2L of distilled water, 12L of tetrahydrofuran, fully stirred for 1.5 hours, centrifuged, and the residue was repeatedly extracted once with 3L of tetrahydrofuran. Combine the extracts, add 4.5L of n-hexane, carry out multiple partitioning for 1.5 hours, obtain the lower polar solvent phase after layering, and extract the upper non-polar solvent phase with 1L of distilled water once, combine the water phase twice, filter, and reduce pressure at 45°C Concentrated, freeze-dried. The finished product is white or off-white, with a purity of 80.5%.
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