System and method suitable for culturing and real-time monitoring of biological tissue
A real-time monitoring and biological tissue technology, applied in biochemical equipment and methods, biological material sampling methods, tissue cell/virus culture devices, etc., to achieve the effect of solving controllability
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example 1
[0115]Step 1. Take a transfer unit 2100, use a bio-3D printer 1000 to print a bio-3D-printed tissue with hepatocytes in it, and put it into a culture medium (DMEM medium+10% fetal bovine serum+1% penicillin streptomycin ) for 20 days, during which the culture medium was replaced every two days;
[0116] Step 2. Take another transfer unit 2100, print a bio-3D printing tissue with tumor cells in it with a bio-3D printer 1000, and put it into a culture medium (DMEM medium+10% fetal bovine serum+1% green chain Mycin) for 20 days, during which the medium was replaced every two days;
[0117] Step 3. Put the 3D bioprinted tissue containing liver cells and the 3D bioprinted tissue containing tumor cells into the transfer unit 2100, and install the transfer unit 2100 into two different culture chambers on the organ chip 2000;
[0118] Step 4. Put the organ chip 2000 into the connection base 5000, close the base cover 5010 to insert the air guide joint 5042 into the trachea interface;...
example 2
[0134] Step 1. Put the two transfer units 2100 into the two culture chambers on the organ chip 2000 respectively;
[0135] Step 2. Make the printing needle enter the cultivation chamber by adjusting the printing nozzle of the biological 3D printer 1000;
[0136] Step 3. Print the 3D bioprinted tissue with liver cells and the 3D bioprinted tissue with tumor cells on the transfer unit 2100 in the two culture chambers;
[0137] Step 4. Add medium (DMEM medium+10% fetal bovine serum+1% penicillin) to the culture chamber, and perform the operations of steps 4-7 in Example 1;
[0138] Step 5. Cultivate the cells for 20 days, during which the medium is replaced every two days according to step 6 in Example 1;
[0139] Step 6. Execute steps 8-17 in Example 1;
[0140] Step 7. Summarize and analyze the sensing records, cell proliferation results, cell growth state observation records and bio-slice results obtained during the experiment to obtain the hepatocytes and tumor cells on the...
example 3
[0142] Step 1. Execute steps 1-10 in Example 1;
[0143] Step 2. When the concentration of the marker is insufficient or the response speed of the sensor chip is insufficient to cause the medium to flow through, the obtained sensing signal is too low, stop the circulation mode in the drive system 3000, and switch to the alternate mode, set 3 clockwise Pause for 5 seconds after the cycle to perform 2 counterclockwise cycles, the cycle frequency is 0.5Hz, the positive pressure output value is 150kPa, the negative pressure output value is 65kPa, and then the alternate mode is turned on;
[0144] Step 3. Execute steps 9-17 in Example 1, wherein, in step 17, "stop the cycle mode in the drive system 3000" is changed to "stop the alternate mode in the drive system 3000";
[0145] Step 4. Summarize and analyze the sensing records, cell proliferation results, cell growth state observation records and bio-slicing results obtained during the experiment to obtain the hepatocytes and tumor...
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