Extracellular polysaccharide complex of Chlorella protothecoides with immunity regulation activity, and preparation method and application thereof
An immunomodulatory activity and extracellular polysaccharide technology, which is applied in the directions of organic active ingredients, medical preparations containing active ingredients, and applications, and can solve the application of less researched and no Chlorella protothecoides exopolysaccharides and their complexes. Value and other issues, to achieve the effect of simple preparation, reduction of inflammatory factors ROS, and cost reduction
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Embodiment 1
[0038] Preparation of Chlorella exopolysaccharide complex with immunomodulatory activity
[0039] (1) Inoculate Chlorella protothecoides CS-41 on Basal solid medium, and culture it under 28°C and 2000Lux light conditions for 5 days to rejuvenate the algae; pick the rejuvenated Chlorella and transfer it to common In the Basal liquid culture medium, 2000Lux (12h light: 12h darkness is carried out alternately), 28 ℃, 160rpm concurrent culture 5 days, obtains first-class seed liquid; 5% first-class seed liquid is inoculated in the fresh liquid medium, isotropic Obtain secondary seed liquid after cultivating for 5 days;
[0040] (2) Get 1% secondary seed liquid to expand and cultivate in the Basal liquid medium that contains 10‰NaCl salinity (about 2.784g / L), the light intensity is 2000Lux, and the light cycle is 8h light: 16h dark (light- Darkness is carried out alternately) under the condition of 28 ℃, 160rpm concurrent culture culture 7 days, obtain the chlorella fermented liquid...
Embodiment 2
[0045] Composition, Purity and Molecular Weight Determination of Chlorella exopolysaccharide complexes with immunomodulatory activity
[0046] (1) Determination of sugar content
[0047] Take 0, 0.05mL, 0.1mL, 0.15mL, 0.2mL and 0.25mL glucose standard solution (100μg / mL) respectively, make up to 0.25mL with distilled water, and add 1mL of anthrone (mass percentage: 0.2%)-sulfuric acid solution, mix well; after boiling water bath for 10 minutes, quickly stop the reaction in ice bath, and then equilibrate to room temperature. Detect its absorbance value at 620nm by a spectrophotometer, and take the glucose concentration as the abscissa, and use the OD 620 As the ordinate, make a standard curve. At the same time, take 2 μL of the aqueous solution (10 mg / mL) of the chlorella exopolysaccharide complex and make up to 0.25 mL with distilled water. The other steps are the same as above, and the sugar content is calculated according to the standard curve.
[0048] (2) Determination ...
Embodiment 3
[0053] Monosaccharide composition and fatty acid composition analysis of exopolysaccharide complexes of Chlorella algae with immunomodulatory activity
[0054] (1) Monosaccharide composition
[0055] Weigh 20mg of dried chlorella exopolysaccharide CPEPS-2, add 10mL trifluoroacetic acid (2mol / L), hydrolyze at 110°C for 6h; add 2mL methanol after drying the hydrolyzate, evaporate to dryness under reduced pressure, repeat 3-4 times , to remove trifluoroacetic acid; then the sample was mixed with 10 mg of hydroxylamine hydrochloride and 0.6 mL of pyridine, and reacted in a water bath at 90 ° C for 30 min; after cooling, 0.5 mL of acetic anhydride was added to continue the reaction at 90 ° C for 30 min; the reaction product was dried and dissolved in 1 mL of chloroform. GC-MS analysis. Chromatographic conditions: HP-5 chromatographic column, injection volume: 2 μL, inlet temperature: 250°C, flow rate 1mL / min; heating program: keep at 110°C for 2 minutes, increase temperature from ...
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