Hi everyone!
I am working on a bioreactor measuring pressure differences. We have introduced a membrane with cells inside a chamber, which creates the pressure differences. The cell media is introduced in the system with a constant flow. The set up is located in the incubator at 37ºC and 5% Co2.
However, we are afraid the chamber does not allow the proper gas exchange. Although the cell media does not change its color (maintains reddish color, no pH alterations) after overnight trials (~20h), we are afraid the cells enter in hypoxia.
To overcome this problem, we are thinking of previously bubbling the cell media with oxygen and then infusing trough the system.
Is this a logical approach? Could it work? Has someone other ideas?
Pd: It is important to avoid any kind of bubbles in the system because alterations in pressure reads could happen.
Thank you very much!