Feedback control in microfluidic systems
Systems and methods for controlling fluids in microfluidic systems are generally described. In some embodiments, control of fluids involves the use of feedback from one or more processes or events taking place in the microfluidic system. For instance, a detector may detect one or more fluids at a measurement zone of a microfluidic system and one or more signals, or a pattern of signals, may be generated corresponding to the fluid(s). In some cases, the signal or pattern of signals may correspond to an intensity, a duration, a position in time relative to a second position in time or relative to another process, and/or an average time period between events. Using this data, a control system may determine whether to modulate subsequent fluid flow in the microfluidic system. In some embodiments, these and other methods can be used to conduct quality control to determine abnormalities in operation of the microfluidic system.
1. A method, comprising:
introducing at least a portion of a fluid sample into a first measurement zone of a microfluidic system;
measuring light transmittance or light absorbance through the fluid sample at the first measurement zone;
forming a signal corresponding to the fluid sample at the first measurement zone,
wherein an intensity of the signal is indicative of the fluid sample at the first measurement zone, and wherein a duration of the signal is indicative of a volume and/or flow rate of the fluid sample at the first measurement zone; and
determining whether to cease an analysis being performed in the microfluidic system based at least in part on information derived from the intensity and/or duration of one or more signals from the fluid sample; and/or alerting a user of an abnormality in an analysis being conducted in the microfluidic system based at least in part on information derived from the intensity and/or duration of one or more signals from the fluid sample.
2. A method as in claim 1 , comprising introducing at least a portion of the fluid sample into a second measurement zone of the microfluidic system, measuring light transmittance or light absorbance through the fluid sample at the second measurement zone, and forming a signal corresponding to the fluid sample at the second measurement zone.
3. A method as in claim 2 , comprising determining whether to cease an analysis being performed in the microfluidic system and/or alerting a user of an abnormality in an analysis being conducted in the microfluidic system based at least in part on information derived from the signal from the fluid sample at the first measurement zone and the signal from the fluid sample at the second measurement zone.
4. A method as in claim 3 , comprising reducing the flow rate of the fluid sample based at least in part on the signal corresponding to the fluid sample at the first measurement zone and the signal from the fluid sample at the second measurement zone.
5. A method as in claim 4 , wherein reducing the flow rate comprises stopping flow of the fluid sample.
6. A method as in claim 1 , comprising reducing the flow rate of the fluid sample based at least in part on the signal corresponding to the fluid sample at the first measurement zone.
7. A method as in claim 6 , wherein reducing the flow rate comprises stopping flow of the fluid sample.
8. A method as in claim 1 , comprising determining flow rate of the fluid sample, and determining whether to cease an analysis being performed in the microfluidic system and/or alerting a user of an abnormality in an analysis being conducted in the microfluidic system based at least in part on the flow rate of the fluid sample.
9. A method as in claim 8 , wherein the flow rate of the fluid sample is a first flow rate, the method comprising reducing the flow rate of the fluid sample to a second flow rate based at least in part on the first flow rate.
10. A method as in claim 9 , wherein the second flow rate is zero.
11. A method as in claim 1 , comprising determining whether to cease an analysis being performed in the microfluidic system and/or alerting a user of an abnormality in an analysis being conducted in the microfluidic system based at least in part on the intensity and duration of the signal corresponding to the fluid sample at the first measurement zone.
12. A method as in claim 11 , comprising reducing the flow rate of the fluid sample based at least in part on the intensity and duration of the signal corresponding to the fluid sample at the first measurement zone.
13. A method as in claim 12 , wherein reducing the flow rate comprises stopping flow of the fluid sample.
14. A method as in claim 11 , comprising alerting a user of an abnormality in an analysis being conducted in the microfluidic system based at least in part on the intensity and duration of the signal corresponding to the fluid sample at the first measurement zone.
15. A method as in claim 1 , wherein the sample comprises whole blood.
16. A method as in claim 1 , wherein the sample is serum or plasma.
17. A method as in claim 1 , comprising continuously or periodically detecting the passing of any fluids across the first and a second measurement zone of the microfluidic system, wherein the first and second measurement zones are positioned in series with respect to one another.
18. A method as in claim 1 , comprising continuously or periodically detecting the passing of any fluids across the first measurement zone.
19. A method as in claim 18 , comprising forming signals corresponding to the passing of each fluid passing across the first measurement zone.
20. A method as in claim 19 , wherein an intensity of each signal is indicative of the concentration of a component in a fluid and/or the amount of a component in a fluid passing across the first measurement zone.
21. A method as in claim 19 , wherein the intensity of each signal is indicative of the type of fluid passing across the first measurement zone.
22. A method as in claim 1 , comprising determining whether to cease an analysis being performed in the microfluidic system and/or alerting a user of an abnormality in an analysis being conducted in the microfluidic system based at least in part on the timing of the signal corresponding to the fluid sample at the first measurement zone.
23. A method as in claim 1 , wherein the intensity of the signal is determined by an opacity of the sample.
24. A method as in claim 1 , wherein the signal is produced absent a label.