Efficient separation and analysis method for active ingredients in enteromorpha prolifera
A technology for separation and analysis of active components, applied in the field of efficient separation and analysis of active components in Enteromorpha, which can solve problems such as low yield, unsatisfactory purification effect, and short service life
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Embodiment 1
[0034] Sample extraction:
[0035] The dried strips of Enteromorpha enteromorpha (1 kg) were completely pulverized into powder, extracted with 3 L of 60% ethanol for 3 times, each time for 3 days, and then the extract was filtered using a vacuum filter. All extracts were combined and concentrated to no alcohol smell, and then the concentrate was extracted with an equal amount of ethyl acetate. The ethyl acetate fraction was rotary evaporated to dryness at 55 °C to obtain 10 g of crude sample, which was stored in a refrigerator at 4 °C for further HSCCC purification.
[0036] Enrichment of polyphenolic compounds in Enteromorpha segmented by gradient countercurrent chromatography:
[0037] The two-phase solvent system tert-butyl methyl ether / n-butanol / acetonitrile / water (4:0:1:5, v / v) and tert-butyl methyl ether / n-butanol / acetonitrile / water (3:1:1:5, v / v) Prepare the solvent system according to the above solvent ratio respectively, put it in a separatory funnel, shake it up an...
Embodiment 2
[0048] The difference from Example 1 is that the upper phase is directly eluted and enriched using tert-butyl methyl ether / n-butanol / acetonitrile / water (3:1:1:5, v / v) solvent system, and the remaining steps are the same as in Example 1 same, the result is as image 3 shown.
[0049] Depend on image 3 It can be seen that if only a two-phase solvent system is used, the effective components cannot be separated.
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