Huidouba polysaccharide and preparation method thereof
A technology of Glycyrrhizae polysaccharides and polysaccharides, which is applied in the field of Glycyrrhizae polysaccharides and its preparation, can solve the problems such as the absence of Glycyrrhizae polysaccharides, achieve the effects of improving glucose tolerance, facilitating industrial production, and improving glucose and lipid metabolism
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Embodiment 1
[0035] Embodiment 1: the preparation of polysaccharide
[0036] Weigh 200g of the dry raw material of Douba huidouba, add 6L deionized water, extract at 95°C for 3h, filter through 400 mesh gauze, repeat the extraction twice under the same operating conditions, combine the extracts, and centrifuge at 4000rmp / min for 10min to obtain Supernatant: Add 200g of activated carbon to the supernatant, shake at 55°C for 2.5h, and centrifuge at a speed of 8000rmp / min for 15min to obtain the supernatant, which is light yellow; add 1250mL of Sevag reagent to the supernatant, and stir magnetically for 15min. Stand still in the separatory funnel for 15-20min, remove the middle layer and the lower layer, keep the upper layer, repeat the operation 8 times, add absolute ethanol to make the final ethanol volume fraction 80-90%, and stand at 0-4°C for 12- 24 hours; centrifuge, collect the precipitate, and freeze-dry to obtain the solid powder of Douba polysaccharide.
Embodiment 2
[0037] Embodiment 2: the preparation of polysaccharide
[0038] Weigh 200g of the dry raw material of Douba huidouba, add 6L deionized water, extract at 95°C for 3h, filter through 400 mesh gauze, repeat the extraction twice under the same operating conditions, combine the extracts, and centrifuge at 4000rmp / min for 10min to obtain Supernatant: Add 200g of activated carbon to the supernatant, shake at 55°C for 2.5h, and centrifuge at a speed of 8000rmp / min for 15min to obtain the supernatant, which is light yellow; add 1250mL of Sevag reagent to the supernatant, and stir magnetically for 15min. Let it stand in the separatory funnel for 15-20 minutes, remove the middle and lower layers, keep the upper layer, and repeat the operation 8 times. The supernatant was purified and graded with a 10kDa ultrafiltration membrane, and the solutions flowing out from the retentate end and the permeate end were collected to obtain polysaccharide 1 and polysaccharide 2 respectively; absolute e...
Embodiment 3
[0039] Embodiment 3: Molecular weight determination of polysaccharide
[0040] The molecular weight of polysaccharides was determined by high performance gel permeation chromatography (GPC). The chromatographic conditions used are: TSK-GEL G-5000PWXL column (7.8mm×300mm) chromatographic column connected in series with TSK-GEL G-3000PWXLcolumn (7.8mm×300mm) chromatographic column; 0.02mol / L KH at pH6.0 2 PO 4 The solution was used as the mobile phase, and the flow rate was 0.6mL / min; the column temperature was 35°C; the detector was a waters 2414 differential detector; Dextran series dextran was used as the standard. The GPC gel permeation chromatograms of polysaccharide 1 and polysaccharide 2 are as follows: figure 1 and figure 2 shown. The average molecular weights of polysaccharide 1 and polysaccharide 2 were 36571Da and 6277Da respectively.
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