Methods and devices for multi-step cell purification and concentration
Described herein are microfluidic devices and methods that can separate and concentrate particles in a sample.
1. A system for separating white blood cells or stem cells from platelets in a sample, the system comprising:
a) a microfluidic channel comprising a first array of obstacles wherein said obstacles have a polygonal cross-section and are configured to separate cells by deterministic lateral displacement (DLD) based on their sizes, such that white blood cells or stem cells flow in a first direction and platelets flow in a second direction different from the first direction;
b) a magnetic separator comprising one or more hard magnets, soft magnets, electromagnets, superconductor magnets, or combination thereof configured to separate particles or cells with magnetically susceptible labels from particles or cells without magnetically susceptible labels, wherein the first array of obstacles is fluidically connected with the magnetic separator;
c) a particle sensor which is fluidically connected to the DLD array or magnetic separator and which, in response to particles or cells with magnetically susceptible labels arriving in a sensing zone, generates an actuation signal to create an actuation event;
d) a particle dispenser fluidically connected to the DLD array or magnetic separator for dispensing particles to a particle collector, wherein the particle dispenser comprises:
i) a fluidic duct configured to allow particles to flow into the fluid duct in a flow stream;
ii) the particle sensor of paragraph c); and
iii) a switch configured to receive the actuation signal.
2. The system of claim 1 , wherein the particle sensor includes a computer module.
3. The system of claim 1 , wherein the actuation signal is caused by magnetically labeled cells and due to a change in impedance, or due to light scatter, morphological, colorimetric, or fluorescent spectral signature or a combination thereof.
4. The system of claim 3 , wherein the actuation signal is caused by magnetically labeled cells and due to a change in impedance.
5. The system of claim 1 , wherein the particle sensor measures impedance.
6. The system of claim 1 , wherein the first array of obstacles is upstream from the magnetic separator; and the system, further comprises:
c) at least a second array of obstacles fluidically connected with the first array of obstacles and the magnetic separator wherein the second array has a critical size different from the critical size of the first array and is downstream from the magnetic separator.
7. The system of claim 1 , wherein a vertex of each of two adjacent obstacles points toward each other in a direction substantially perpendicular to a flow direction of the sample through the array of obstacles.
8. The system of claim 7 , wherein the DLD array comprises an array of obstacles that have a cross-sectional shape of a hexagon or are diamond-shaped.
9. The system of claim 1 , wherein the DLD array comprises an array of obstacles with a critical diameter of from about 1 μm to about 5 μm.
10. The system of claim 1 , wherein the particles or cells with magnetically susceptible labels are white blood cells or stem cells and the actuation signal is in response to the flow of these cells with magnetically susceptible labels into the sensing zone.
11. The system of claim 10 , wherein the particle dispenser further comprises: d) a capture tube, wherein the capture tube is movable between a first position and a second position, wherein capture tube is not fluidically connected with the fluidic duct at the first position, and is fluidically connected with the fluidic duct at the second position, wherein the capture tube remains at the first position unless driven by the switch, wherein the switch drives the capture tube from the first position to the second position after receiving the actuation signal.
12. The system of claim 1 , wherein the magnetic separator comprises one or more microfluidic channels, wherein at least one microfluidic channel in the magnetic separator is 200-1600 μm in width and wherein at least one microfluidic channel in the magnetic separator comprises one or more posts disposed along the center of the channel.
13. The system of claim 1 , wherein, during operation, the system comprises a sample which has one or more additives that block the adhesion or activation of platelets.