Claims
- 1) an improved method for manipulating small particles in a microfluidic system wherein at least one tolerance of the microfluidic system is greater than the size of the small particles, the improvement comprising providing a layer of large particles, said large particles being sufficiently small enough to capture the small particles, but sufficiently large to not escape through the tolerances within the microfluidic system.
- 2) The improved method of claim 1 further comprising providing the layer of large particles as a mixture with the small particles in a fluid flow through the microfluidic system.
- 3) The improved method of claim 1 further comprising first providing the layer of large particles in a fluid flow of the microfluidic system into a region of the microfluidic system having the tolerance, wherein the large particles are stopped by the tolerance and the fluid flow is allowed and to pass through the tolerance, and subsequently providing the small particles in the fluid flow, thereby trapping the small particles above or within the large particles and allowing the fluid flow to pass through the tolerance.
- 4) The improved method of claim 1 further wherein the small particles are provided as having a diameter of between about 5 and 6 microns.
- 5) The improved method of claim 1 further wherein the large particles are provided as having a diameter of about 20 microns.
- 6) The improved method of claim 1 wherein particles are selected from the group consisting of Sr-resin, TRU-resin, TEVA-resin, glass, Sepharose, polystyrene, Tepnel, Qiagen, zirconium, hydroxyapatite, POROS, PEG-PS, PS, and polymeric micro-beads covalently linked to specific oligonucleotide capture probes.
- 7) An improved method for manipulating small particles having a diameter of between about 5 and 6 microns in a microfluidic system wherein at least one tolerance of the microfluidic system is greater than the size of the small particles, the improvement comprising providing a layer of large particles, said large particles being sufficiently small enough to capture the small particles, but sufficiently large to not escape through the tolerances within the microfluidic system.
- 8) The improved method of claim 7 further comprising providing the layer of large particles as a mixture with the small particles in a fluid flow through the microfluidic system.
- 9) The improved method of claim 7 further comprising first providing the layer of large particles in a fluid flow of the microfluidic system into a region of the microfluidic system having the tolerance, wherein the large particles are stopped by the tolerance and the fluid flow is allowed and to pass through the tolerance, and subsequently providing the small particles in the fluid flow, thereby trapping the small particles above or within the large particles and allowing the fluid flow to pass through the tolerance.
- 10) The improved method of claim 7 further wherein the large particles are provided as having a diameter of about 20 microns.
- 11) The improved method of claim 7 wherein particles are selected from the group consisting of Sr-resin, TRU-resin, TEVA-resin, glass, Sepharose, polystyrene, Tepnel, Qiagen, zirconium, hydroxyapatite, POROS, PEG-PS, PS, and polymeric micro-beads covalently linked to specific oligonucleotide capture probes.
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This is a Continuation in Part of U.S. patent application Ser. No. 09/177,902 filed Oct. 23, 1998, now U.S. Patent ______.
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT
[0002] This invention was made with Government support under Contract DE-AC0676RL01830 awarded by the U.S. Department of Energy. The Government has certain rights in the invention.
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
09177902 |
Oct 1998 |
US |
Child |
10132498 |
Apr 2002 |
US |