Preparation method of exosome and stem cell proliferation reagent containing exosome
A technology of stem cell proliferation and exosomes, applied in the field of bioengineering, can solve the problem of no large-scale cell expansion, easy to meet quality standards, easy to use, and harmless ingredients
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Embodiment 1
[0035] Example 1 Preparation of bone marrow mesenchymal stem cell exosomes
[0036] 1. Preparation of bone marrow mesenchymal stem cell supernatant:
[0037] The bone marrow mesenchymal stem cells of the third generation in the logarithmic phase of growth were digested, and an appropriate amount of medium without exosome serum was added to make a cell suspension, which was inoculated in a T25 cell culture flask, and the cell culture medium was harvested after 60 hours. The supernatant was collected to reach more than 200ml, and the exosomes were extracted.
[0038] 2. Isolation and storage of exosomes from bone marrow mesenchymal stem cells:
[0039]Centrifuge the supernatant collected above at 4°C, 400×g for 10 minutes, transfer the supernatant to remove cell debris; centrifuge at 4°C, 2000×g for 10 minutes, transfer the supernatant to remove dead cells; Filter the supernatant to further remove impurities; 4°C, 120,000×g, ultracentrifuge for 150 minutes to precipitate exoso...
Embodiment 2
[0044] Example 2 Separation, Purification and Culture of Human Umbilical Cord Mesenchymal Stem Cells
[0045] First, discard the excess preservation solution in the fresh umbilical cord obtained from the hospital, pour 75% alcohol into it for disinfection for three minutes, then take out the umbilical cord, put it in normal saline with double antibody and wash it repeatedly to remove the residual alcohol on the surface. Cut off the ligated part and discard it. Divide the remaining umbilical cord evenly into small pieces for cleaning, wash the residual blood repeatedly, remove the umbilical vein and umbilical artery, peel off the Wharton glue, and cut it to 1mm 3 The size of the organization block. According to the amount of tissue pieces, add an appropriate amount of conventional medium, mix evenly, spread it on a 15cm petri dish, and place it at 37°C, 5% CO 2 And culture in a humidity-saturated incubator for 24 hours, and add 8ml of culture solution to each dish. Replenish ...
Embodiment 3
[0046] Example three cell function test
[0047] 1. Preparation of exosome culture medium:
[0048] After the exosomes obtained above were taken out from -80°C and thawed, they were added to the culture medium of human umbilical cord mesenchymal stem cells at a final concentration of 20 μg / ml, and stirred evenly.
[0049] Second, the cell proliferation test steps are as follows
[0050] Human umbilical cord mesenchymal stem cells in the logarithmic growth phase of 10 passages were digested, resuspended in human umbilical cord mesenchymal stem cell culture medium supplemented with bone marrow mesenchymal stem cell exosomes, and mixed with 2×10 4 Inoculate in a 24-well plate, 500L / well, at 37°C, 5% CO 2 , 95% O 2 Cultured in an incubator, set up a blank control group. After culturing for 24 hours, trypsinize the cells in the three wells for 2 minutes at room temperature, collect the cells in each well, centrifuge at 1200r for 5 minutes, resuspend with a small amount of mediu...
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