Oligomeric guluronic acid phosphate as well as preparation method and application thereof
A technology of guluronic acid phosphate and polyguluronic acid, which is applied in the fields of marine medicine and immune enhancer, can solve the problem of high industrialization cost, achieve low production cost, significant immune enhancement effect, and enhance humoral immunity. and cellular immunity
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Embodiment 1
[0025] Example 1: Preparation of oligomeric guluronic acid phosphate
[0026] The raw material used in the present invention is oligomeric guluronic acid (purity>80%, weight-average molecular weight<20kDa) which is obtained through degradation and classification of alginate, and existing oligomeric guluron in the prior art can also be used aldehyde acid. Weigh 10 g of oligomeric guluronic acid into a reaction flask, add 180 g of urea, add 800 mL of N,N-dimethylformamide, and then add 70 mL of phosphoric acid (mass volume ratio is 85%), and stir evenly. The suspension formed by mixing the above components was refluxed at 130° C. for 4 hours. After the reaction is over, collect the reaction precipitate, wash it repeatedly with 95% ethanol and dissolve it in water, adjust the pH of the solution to 8-9 with NaOH, then use semi-permeable membrane dialysis to remove residual urea and phosphate during the reaction, spray dry, The oligomeric guluronic acid phosphate is obtained.
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Embodiment 2
[0036] Example 2: Immunopotentiation of oligomeric guluronic acid phosphate
[0037] According to the internationally recognized method, the immune enhancing effect of oligomeric guluronic acid phosphate was evaluated at the animal level.
[0038] 1) Effects on body weight and immune organ / body weight ratio of immunocompromised mice
[0039] Take 72 SPF-level Kunming mice (18-22g) and feed them adaptively for 3 days, and then randomly divide them into 6 groups, 12 mice in each group, which are blank group, model group, low polyguluronic acid phosphate , medium and high dose groups and lentinan group. The administration was administered by intragastric administration for 10 consecutive days; except for the blank group, the mice in the other groups were intraperitoneally injected with cyclophosphamide 100 mg / kg·d on the sixth day of administration to establish a model. 24 hours after the last administration, the mice were weighed, sacrificed by cervical dislocation, the spleen a...
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