Systems and methods for biomimetic fluid processing
Systems and methods generating physiologic models that can produce functional biological substances are provided. In some aspects, a system includes a substrate and a first and second channel formed therein. The channels extend longitudinally and are substantially parallel to each other. A series of apertures extend between the first channel and second channel to create a fluid communication path passing through columns separating the channels that extends further along the longitudinal dimension than other dimensions. The system also includes a first source configured to selectively introduce into the first channel a first biological composition at a first channel flow rate and a second source configured to selectively introduce into the second channel a second biological composition at a second channel flow rate, wherein the first channel flow rate and the second channel flow rate create a differential configured to generate physiological shear rates within a predetermined range in the channels.
1. A method for producing a biological substance, the method comprising:
introducing, through a first flow filter, a first biological composition into a first channel of a microfluidic system at a first channel flow rate, the first biological composition including a biological source material capable of producing a target biological substance;
introducing, through a second flow filter, a second biological composition into a second channel of the microfluidic system at a second channel flow rate;
selectively capturing, by a membrane separating the first channel and the second channel and forming a fluid communication path between the first channel and the second channel, the biological source material from the first biological composition passing through the membrane;
generating physiological shear rates on the captured biological source material that induce the captured biological source material to produce the target biological substance; and
harvesting, using the second biological composition, the produced target biological substance from the second channel.
2. The method of claim 1 , wherein the microfluidic system further comprises a substrate in which the first channel and the second channel are formed.
3. The method of claim 1 , wherein the first channel extends from a first input to a first output substantially along a longitudinal direction and the second channel extends from a second input to a second output along the longitudinal direction, wherein at least a portion of the first and second channels extends substantially parallel along the longitudinal direction.
4. The method of claim 3 , wherein the membrane separates the first channel and the second channel along a transverse direction.
5. The method of claim 3 , wherein a first flow resistor positioned between the first input and the first flow filter; and a second flow resistor positioned between the second input and the second flow filter.
6. The method of claim 1 , wherein generating physiological shear rates comprises adjusting the first channel flow rate and the second channel flow rate to create a differential between the first channel and the second channel that generates physiological shear rates along the second channel.
7. The method of claim 1 , wherein the membrane includes a plurality of pores sized less than the biological source material to allow capture of the biological source material generally about the pores.
8. The method of claim 7 , wherein the pores have a diameter in a range between 3 micrometers and 12 micrometers.
9. The method of claim 1 , wherein the physiological shear rates are in a range between 100 s-1 and 10,000 s-1.
10. A method for producing a biological substance, the method comprising:
introducing, through a first flow filter, a first biological composition into a first channel of a microfluidic system at a first channel flow rate, the first biological composition including a biological source material, wherein the biological source material comprises megakaryocytes (MKs) capable of generating platelets (PLTs);
introducing, through a second flow filter, a second biological composition into a second channel of the microfluidic system at a second channel flow rate;
selectively capturing, by a membrane separating the first channel and the second channel and forming a fluid communication path between the first channel and the second channel, the MKs from the first biological composition passing through the membrane;
generating physiological shear rates on the MKs that induce the captured MKs to produce the PLTs; and
harvesting, using the second biological composition, the produced PLTs from the second channel.
11. The method of claim 10 , wherein generating physiological shear rates comprises adjusting the first channel flow rate and the second channel flow rate to create a differential between the first channel and the second channel that generates physiological shear rates along the second channel.
12. The method of claim 10 , wherein the physiological shear rates are in a range between 100 s −1 and 10,000 s −1 .