Preparation method and application deep sea water and fucoidin composite liquid
A technology of deep ocean water and fucoidan, applied in the field of marine biology, can solve the problems of insulin resistance and metabolic diseases that have not been reported, and achieve the effects of reducing glycogen output, regulating insulin signaling pathway, and strengthening the regulatory effect
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Embodiment 1
[0039] Embodiment 1. Preparation method of deep ocean water and fucoidan compound solution
[0040] 1. The preparation method of deep ocean water with hardness of 1000ppm
[0041] Put the deep ocean water taken from 20km away from the coastline and 500m deep at the sea level into the water storage tank, filter it with a filter to remove phytoplankton and microorganisms in the seawater, and filter it through an activated carbon filter to further remove organic matter; the pretreatment The obtained deep ocean water enters the reverse osmosis device through a high-pressure pump to divide the deep ocean water into fresh water and concentrated water (the water quality of the fresh water is the same as that of pure water, or the water quality is close to pure water); the separated concentrated water is concentrated under reduced pressure, Concentrate its volume to 0.67-3.33% of the original volume, and then filter and remove the precipitated sodium chloride to obtain a highly concen...
Embodiment 2
[0046] Example 2. The improvement effect and mechanism of the compound solution of deep ocean water and fucoidan on insulin resistance
[0047] 1. Experimental method
[0048] 1) Cell culture: human liver cancer cells HepG2 cells, the cell culture medium is low-sugar DMEM (5.5mmol / L) medium containing 10% fetal bovine serum, the culture environment is 37 ° C, 5% CO2, every 3 days by 1:3 Ratio passaging once.
[0049] 2) Cytotoxicity of the compound solution of deep ocean water and fucoidan on HepG2 cells: collect the logarithmic phase cells, adjust the concentration of the cell suspension and inoculate them in a 96-well plate with 10,000 cells per well. 37°C, 5% CO 2 Culture, when the cell confluency reaches 70%, replace with serum-free DMEM, starve overnight, then add deep ocean water with a hardness of 1000ppm and different concentrations of fucoidan (5, 10, 50, 100, and 500mg / L) ) compound solution, 6 parallel wells were set up for each concentration. Continue culturing...
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