Method for continuous particle separation using obstacle arrays asymmetrically aligned to fields
The present invention relates to methods and devices for separating particles according to size. More specifically, the present invention relates to a microfluidic method and device for the separation of particles according to size using an array comprising a network of gaps, wherein the field flux from each gap divides unequally into subsequent gaps. In one embodiment, the array comprises an ordered array of obstacles in a microfluidic channel, in which the obstacle array is asymmetric with respect to the direction of an applied field.
1. A microfluidic device for concentrating particles, having at least a predetermined critical size, the device comprising:
a microfluidic channel, an ordered array of obstacles within the microfluidic channel, and a boundary, wherein
the device employs a field that propels particles through the microfluidic channel; and
the ordered array of obstacles is asymmetric with respect to the average direction of the field, such that, when particles are introduced into the array, particles having a size less than a predetermined critical size are transported in a first direction, and particles having a size at least that of the critical size are transported in a second direction to the boundary, wherein the first and second directions are different, thereby concentrating the particles having a size at least that of the critical size.
2. The microfluidic device of claim 1 , wherein the ordered array of obstacles comprises obstacles arranged in rows, wherein each subsequent row of obstacles is shifted laterally with respect to the previous row.
3. The microfluidic device of claim 1 , wherein the ordered array of obstacles is tilted at an offset angle θ with respect to the direction of the field.
4. The microfluidic device of claim 1 , wherein the field is fluid flow, electrical, electrophoretic, electro-osmotic, centrifugal, gravitational, hydrodynamic, pressure gradient, or capillary action.
5. The microfluidic device of claim 4 , wherein the field is a fluid flow.
6. The microfluidic device of claim 4 , wherein the field is an electrical field.
7. The microfluidic device of claim 1 , wherein the particles are bacteria, cells, organelles, viruses, nucleic acids, proteins, protein complexes, polymers, powders, latexes, emulsions, or colloids.
8. The microfluidic device of claim 7 , wherein the particles are DNA molecules.
9. A method for concentrating particles, having at least a predetermined critical size, the method comprising:
introducing particles into a microfluidic channel comprising a network of gaps within the microfluidic channel and a boundary; and applying a field to the particles to propel the particles through the microfluidic channel, wherein a flux of the field from the gaps is divided unequally into a major flux component and a minor flux component into subsequent gaps in the network, such that the average direction of the major flux component is not parallel to the average direction of the field, and particles having a size less than a predetermined critical size are transported generally in the average direction of the field, and particles having a size at least that of the critical size are transported generally in the average direction of the major flux component to the boundary, thereby concentrating the particles having a size at least that of the critical size.
10. The method of claim 9 , wherein the network of gaps is constructed from an array of obstacles.
11. The method of claim 10 , wherein the array of obstacles is an ordered array of obstacles.
12. The method of claim 11 , wherein the ordered array of obstacles comprises obstacles arranged in rows, wherein each subsequent row of obstacles is shifted laterally with respect to the previous row.
13. The method of claim 11 , wherein the ordered array of obstacles is tilted at an offset angle θ with respect to the direction of the field.
14. The method of claim 9 , wherein the field is fluid flow, electrical, electrophoretic, electro-osmotic, centrifugal, gravitational, hydrodynamic, pressure gradient, or capillary action.
15. The method of claim 14 , wherein the field is a fluid flow.
16. The method of claim 14 , wherein the field is an electrical field.
17. The method of claim 9 , wherein the particles are bacteria, cells, organelles, viruses, nucleic acids, proteins, protein complexes, polymers, powders, latexes, emulsions, or colloids.
18. The method of claim 17 , wherein the particles are DNA molecules.
19. A method for concentrating particles, having at least a predetermined critical size, the method comprising:
introducing particles into a microfluidic channel, comprising an ordered array of obstacles and a boundary; and
applying a field to the particles to propel the particles through the microfluidic channel, wherein the ordered array of obstacles is asymmetric with respect to the average direction of the field, such that particles having a size less than a predetermined critical size are transported in a first direction, and particles having a size at least that of the critical size are transported in a second direction to the boundary, wherein the first and second directions are different, thereby concentrating the particles having at least the predetermined critical size.
20. The method of claim 19 , wherein the ordered array of obstacles comprises obstacles arranged in rows, wherein each subsequent row of obstacles is shifted laterally with respect to the previous row.
21. The method of claim 19 , wherein the ordered array of obstacles is tilted at an offset angle θ with respect to the direction of the field.
22. The method of claim 19 , wherein the field is fluid flow, electrical, electrophoretic, electro-osmotic, centrifugal, gravitational, hydrodynamic, pressure gradient, or capillary action.
23. The method of claim 22 , wherein the field is a fluid flow.
24. The method of claim 22 , wherein the field is an electrical field.
25. The method of claim 19 , wherein the particles are bacteria, cells, organelles, viruses, nucleic acids, proteins, protein complexes, polymers, powders, latexes, emulsions, or colloids.