Use of ocean green algae in extraction of cyclic peptide components with anti-tumor activity
A technology of anti-tumor activity and marine green algae, which is applied in the application field of unicellular multinucleated marine green algae in the extraction of anti-tumor active cyclic peptide components, which can solve the limitation of preparation and utilization of cyclic peptide compounds, limited sea squirt and sponge resources , Breeding difficulties and other problems, to achieve the effect of low cost, good applicability and simple process
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Embodiment 1
[0020] see figure 1 Shown, the preparation process of Bryopsis sp. cyclic peptide fraction.
[0021] Fresh Bryopsis sp., washed 2-3 times quickly with distilled water, squeezed dry, weighed about 1kg; reflux extracted with 2L methanol for 3 times, each 2h, filtered, combined the methanol filtrate obtained 3 times, concentrated under reduced pressure to volume 1 ~1.5L, and then sequentially extracted with equal volumes of n-butanol and chloroform; the n-butanol layer was washed 1-2 times with equal volumes of distilled water, and the n-butanol layer was taken by standing and separated, concentrated under reduced pressure, and dried in vacuo to form components 1. After the chloroform layer was concentrated to dryness under reduced pressure, add 1 L each of methanol-water (volume ratio 9:1) and n-hexane. The layers were separated; the chloroform layer was concentrated under reduced pressure and dried in vacuo to obtain component 2.
[0022] Using ninhydrin as the chromogenic a...
Embodiment 2
[0036] Take fresh moss feather algae (Bryopsis hypnoides), wash them quickly with distilled water twice, squeeze dry, and weigh about 1kg; each time extract with 3L ethanol for 3 times, each 2h, filter, combine the ethanol filtrates obtained three times, and concentrate under reduced pressure to The volume is 1-1.5L, and then extracted with an equal volume of n-butanol and chloroform in sequence. The n-butanol layer was washed with an equal volume of distilled water for 1-2 times, and the n-butanol layer was taken, concentrated under reduced pressure, and dried under vacuum to obtain component 1. After the chloroform layer was concentrated to dryness under reduced pressure, 2 L of methanol-water (volume ratio 8.5:1.5) and 1 L of n-hexane were added, and the methanol layer was taken after standing to separate layers, and the concentration of methanol was adjusted to 80%, and then an equal volume of chloroform was added to statically The layers were separated; the chloroform lay...
Embodiment 3
[0038] Take fresh Bryopsis plumosa, wash it twice quickly with distilled water, squeeze dry, and weigh about 1kg; extract twice with 2.5L ethanol each time, 4h each, filter, combine the ethanol filtrate obtained twice, and depressurize Concentrate to a volume of 1-1.5 L, and then extract with equal volumes of n-butanol and chloroform in sequence; the n-butanol layer is washed once with equal volumes of distilled water, and the n-butanol layer is taken, concentrated under reduced pressure, and vacuum-dried to obtain component 1. After the chloroform layer was concentrated to dryness under reduced pressure, add 0.8 L each of methanol-water (volume ratio 8.5:1.5) and n-hexane. After standing to separate, take the methanol layer, adjust the methanol concentration to 80%, and then add an equal volume of chloroform The layers were separated at rest; the chloroform layer was concentrated under reduced pressure and dried in vacuo to obtain component 2.
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