Placenta preserving fluid
A technology for preserving liquid and placenta, which is applied in the preservation, application, animal husbandry and other directions of human or animal body, can solve the problem of decreased bacterial infection rate of the placenta, and achieve the effect of avoiding the decrease of cell activity.
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Embodiment 1
[0038] The preparation of embodiment 1 placenta preservation solution
[0039] With deionized water as solvent, add 10mmol-15mmol potassium dihydrogen phosphate, 30mmol-40mmol sodium chloride, 40mmol-50mmol potassium chloride, 8mmol-10mmol magnesium sulfate, 70mmol-100mmol histidine, 1.5mmol-2.0mmol allopurine , 45mg-55mg5,7-dihydroxy-3',4'-dimethylflavone, 3mmol reduced glutathione, 1ml-8ml2-mercaptoethanol, 8mol-10mmol adenosine, 20mg-50mg ginsenoside Rg1, 0.01 Mmol-0.08mmol dexamethasone, 100000U-1000000U penicillin, 60mg-100mg streptomycin and 50mg-70mg gentamicin were prepared into 1000ml placental preservation solution, pH7.33-7.83. Subpackage, seal, and store at 0°C-4°C.
Embodiment 2
[0040] The proliferative ability of embodiment 2 cells
[0041] The placenta was preserved in normal saline, and after 5 days, the placenta was taken out and mesenchymal stem cells were isolated (see figure 1 ).
[0042] The placenta was placed in the placenta preservation solution prepared in Example 1, and after 5 days, the placenta was taken out and separated to obtain mesenchymal stem cells (see figure 2 ).
[0043] from figure 1 with figure 2 It can be seen that the morphology of stem cells is better maintained after using the placenta preservation solution. By calculating the number of cells, it is proved that the placental cells proliferating ability is stronger after the placenta preservation solution is preserved, and the number of mesenchymal stem cells cultured at the same time is more. The results are shown in Table 1.
[0044] Table 1
[0045]
Embodiment 3
[0046] The infection rate of embodiment 3 placenta
[0047] The placenta was stored in physiological saline and the placenta preservation solution prepared in Example 1 for 5 days, and then the bacterial infection test was carried out (see Table 2).
[0048] Table 2
[0049]
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