IP Library Granted Patent US 9,149,805
Granted Patent B2
US 9,149,805 · App. 13/913,321 · Granted Oct 6, 2015

Microfluidic fluid separator and related methods

Inventors: Emil P. Kartalov (Pasadena, CA); Axel Scherer (Woodstock, VT); Koichi Sayano (Montebello, CA)
Assignees: UNIVERSITY OF SOUTHERN CALIFORNIA; APIC CORPORATION; CALIFORNIA INSTITUTE OF TECHNOLOGY
B01L3/502753A61M1/3496A61M1/3633A61M1/3472B01L2300/0645B01L2300/0681B01L2300/087B01L2300/0816B01L2300/0864B01L2400/0424Y10T436/25125Y10T436/25375
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Quick Facts
Patent No.
US 9,149,805
App. No.
13/913,321
Granted
Oct 6, 2015
Kind
B2
Abstract

A microfluidic fluid separator for separating target components of a fluid by filtration is described. Methods for separating target components of a fluid by filtration and methods for processing blood on a large scale with the microfluidic fluid separator are provided.

Claims (36)

1. An array of microfluidic filter chips comprising a plurality of microfluidic filter chips, each microfluidic filter chip for separating target components of a fluid by filtration, the target components adapted to exit though a plurality of output terminals of the microfluidic filter chip, the microfluidic filter chip comprising:

a plurality of filtering stages comprising a stack of perforated surfaces including a top perforated surface and a bottom perforated surface,

wherein:

a flow channel is provided above and below each perforated surface,

each perforated surface comprises a plurality of openings through which components of the fluid commensurate with the openings are adapted to pass,

the diameter of the openings in the perforated surfaces decreases sequentially from the top perforated surface to the bottom perforated surface, such that the diameter of the openings of the top perforated surface is larger than the diameter of the openings of all other perforated surfaces in the stack,

an input of the microfluidic filter chip is provided at an entrance of the uppermost flow channel,

an output terminal of the microfluidic filter chip is provided at an end of each flow channel, and

for each stacked perforated surface, the flow channel above the stacked perforated surface is narrower and shallower than the flow channel below the stacked perforated surface,

wherein the plurality of microfluidic filter chips is stacked and a corresponding output terminal of a flow channel of each microfluidic filter chip of the array corresponding to a same filtered particle size range for the microfluidic filter chips of the array is joined together with corresponding output terminals of the microfluidic filter chips of the array.

2. The array of microfluidic filter chips of claim 1 , wherein the array is portable.

3. The array of microfluidic filter chips of claim 1 , further comprising:

at least one electrode adapted to apply an electric field to the microfluidic filter chip.

4. The array of microfluidic filter chips according to claim 1 , wherein the perforated surface comprises polycarbonate, elastomer, or silicon on insulator wafers.

5. A method for separating a fluid by filtration through the array of microfluidic filter chips according to claim 1 , the fluid comprising a plurality of target components, the method comprising:

providing the fluid to the input of the array of microfluidic filter chips; and

directing the target components to corresponding flow channels based on size of the target components, thus separating the fluid.

6. The method according to claim 5 , wherein the plurality of target components are cells, wherein the cells differ in size.

7. The method according to claim 5 , wherein the plurality of target components are biological molecules.

8. The method according to claim 5 , wherein the fluid sample comprises at least one of a protein, a peptide comprising natural and/or unnatural amino acids, an enzyme, natural or synthetic DNA or fragments thereof, and natural or synthetic RNA or fragments thereof.

9. The method according to claim 5 , wherein the fluid is a sample of bodily fluid.

10. The method according to claim 9 , wherein the bodily fluid is a blood and the fluid components are blood components.

11. The method according to claim 10 , wherein the blood components comprise at least one of WBCs, RBCS, platelets, and plasma.

12. The method of claim 5 , further comprising:

applying an electric field to the microfluidic filter chip.

13. The method of claim 12 , wherein the applying an electric field comprises dielectric separation of the target components from contaminants.

14. The method of claim 5 , further comprising:

applying a magnetic field to the microfluidic filter chip.

15. A method to detect at least one target component in a fluid comprising:

performing the method of claim 5 ; and

detecting the at least one target component.

16. The method of claim 15 , wherein the detecting comprises measuring capacitance to detect different types of cells, measuring refractive index, introducing fluorescent labels and measuring fluorescence of fluorescently-labeled species, and/or introducing nanoparticle labels and detecting nanoparticle-labeled species with optical or electromagnetic measurements.

17. A method of point-of-care testing through the array according to claim 1 , the method comprising:

isolating fluid from a patient;

providing the fluid to an input of the array; and

directing the target components to corresponding flow channels based on size of the target components, thus separating the fluid.

Assignments (4)
CONFIRMATORY LICENSE Recorded Sep 27, 2013
From: CALIFORNIA INSTITUTE OF TECHNOLOGY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 031303/0567 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2013
From: SAYANO, KOICHI
To: APIC CORPORATION
Reel/Frame 030766/0446 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2013
From: SCHERER, AXEL
To: CALIFORNIA INSTITUTE OF TECHNOLOGY
Reel/Frame 030766/0587 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 9, 2013
From: KARTALOV, EMIL P.
To: UNIVERSITY OF SOUTHERN CALIFORNIA
Reel/Frame 030762/0651 →
Continuity (3)
Division 13206362 · Aug 9, 2011
Provisional Application 61373216 · Aug 12, 2010
Related Publication 20130267005A1 · Oct 10, 2013