Polar glycolipid extract and application thereof
A polar glycolipid and extract technology, applied in the field of polar glycolipid extract, can solve the problem of slow development of marine active substances, and achieve the effects of increasing the differentiation rate of nerve cells, improving neural differentiation, and improving the neurodevelopment of children
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Embodiment 1
[0018] Embodiment 1: the preparation of sea cucumber lipid crude extract
[0019] The first step is to take the sea cucumber with internal organs removed, freeze-dry at -40°C, grind and sieve to obtain dry powder.
[0020] In the second step, 20 g of sample powder was weighed, leached once with chloroform / methanol (1:2, v / v), vortexed for 1 min and then allowed to stand for 10 min, and the upper layer extract was collected by centrifugation; the residue was washed with chloroform-methanol (3:1 , v / v) and then repeat the leaching for 2 to 3 times, combine the two supernatants and filter to obtain the leaching solution.
[0021] In the third step, add water to the extract and vortex it. After sufficient extraction, centrifuge to collect the upper methanol-water phase; add 0.01mol / L KCl solution and methanol (1:3, v / v) to the lower chloroform solution to extract again , combined the upper solution. Then the sample was loaded on an activated C8 solid-phase extraction column, elu...
Embodiment 2
[0022] Embodiment 2: Preparation of sea cucumber polar glycolipid extract
[0023] In the first step, the edible part of sea cucumber is taken, freeze-dried at -40°C, ground and sieved to obtain dry powder;
[0024] In the second step, 10 g of sample powder was weighed, leached once with chloroform / methanol (1:1, v / v), vortexed for 1 min and then allowed to stand for 10 min; the upper extract was collected by centrifugation, and the residue was washed with chloroform-methanol (1:1 , v / v) after repeated leaching for 2 to 3 times, the two supernatants were combined and filtered to obtain the leaching solution;
[0025] In the third step, add water to the extract and vortex it. After fully extracting, centrifuge to collect the upper methanol-water phase; add 0.01mol / L KCl solution and methanol (1:1, v / v) to the lower chloroform solution to extract again , combined the upper solution. Then load the sample on an activated C8 solid-phase extraction column, elute with methanol, and...
Embodiment 3
[0027] Embodiment 3: the preparation of sea urchin polar glycolipid extract
[0028] The first step is to take the edible part of the sea urchin, freeze-dry it at -40°C, grind it and sieve it to obtain a dry powder;
[0029] In the second step, weigh 40g of the sample powder, extract it once with chloroform / methanol (1:2, v / v), vortex for 1min and then let it stand for 10min; , v / v) after repeated leaching for 2 to 3 times, the two supernatants were combined and filtered to obtain the leaching solution;
[0030] In the third step, add water to the extract and vortex it. After sufficient extraction, centrifuge to collect the upper methanol-water phase; add 0.01mol / L KCl solution and methanol (1:3, v / v) to the lower chloroform solution to extract again , combined the upper solution. Then load the sample on an activated C8 solid-phase extraction column, elute with methanol, and carry out thin-layer silica gel plate chromatography (TLC) on the eluent, wherein the developing solv...
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