IP Library Granted Patent US 7,704,395
Granted Patent B2
US 7,704,395 · App. 11/594,094 · Granted Apr 27, 2010

Multiple laminar flow-based rate zonal or isopycnic separation with holographic optical trapping of blood cells and other static components

Assignee: Arryx, Inc.
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Quick Facts
Patent No.
US 7,704,395
App. No.
11/594,094
Granted
Apr 27, 2010
Kind
B2
Abstract

The invention provides a method and apparatus for separating blood into components, may be expanded to include other types of cellular components, and can be combined with holographic optical manipulation or other forms of optical tweezing. One of the exemplary methods includes providing a first flow having a plurality of blood components; providing a second flow; contacting the first flow with the second flow to provide a first separation region; and differentially sedimenting a first blood cellular component of the plurality of blood components into the second flow while concurrently maintaining a second blood cellular component of the plurality of blood components in the first flow. The second flow having the first blood cellular component is then differentially removed from the first flow having the second blood cellular component. Holographic optical traps may also be utilized in conjunction with the various flows to move selected components from one flow to another, as part of or in addition to a separation stage.

Claims (20)

1. An apparatus for separating a fluid mixture into constituent, non-motile components, the apparatus comprising:

a first separation region having a first inlet and a second inlet, said first inlet introducing a first flow and said second inlet introducing a second flow into said first separation region; means for providing said first flow and said second flow as non-turbulent, laminar flows into said first separation region;

wherein a first component of a plurality of components in said first flow sediment into said second flow to form an enriched second flow and depleted first flow to purify said first flow, while concurrently maintaining a second component of the plurality of components in said first flow;

wherein said first separation region has a first outlet through which said depleted first flow exits to a third inlet of a second separation region, and second outlet into which said enriched second flow is deposited;

wherein said second separation region is an optically transparent sorting region, and includes a fourth inlet through which a third flow enters and a third outlet and a fourth outlet;

a holographic optical trap system coupled to the second separation region, the holographic optical trap system which generates a holographic optical trap to select and move said second component from said depleted first flow into said third flow to form an enriched third flow and a further depleted first flow, said enriched third flow exiting through said third outlet;

wherein said further depleted first flow continues to said fourth outlet, connected to said fourth inlet in first recirculation loop, to recirculate into said second separation region as said third flow, and receives a fourth flow from a fifth inlet downstream form said fourth outlet, connected to said second inlet in second recirculation loop, to recirculate into said first separation region as said second flow.

2. The apparatus of claim 1 , wherein said first component and said second component are blood components that are being sorted.

3. The apparatus of claim 2 , wherein said first component is at least one of red and white blood cells.

4. The apparatus of claim 1 , wherein said first component is undesired components including one of cellular debris and impurities.

5. The apparatus of claim 3 , wherein said second component is platelets.

6. The apparatus of claim 5 , wherein said second flow, said third flow, and said fourth flow, are plasma.

7. The apparatus of claim 1 , further comprising additional separation regions for further sorting, said additional separation regions including one of an additional sedimentation separation region and an additional holographic optical trap system.

8. The apparatus of claim 1 , further comprising at least one inspection region, said inspection region including at least one of an optical inspection technique and a spectroscopic inspection technique.

9. The apparatus of claim 1 , further comprising at least one electronic measurement device to measure any of said flows.

10. The apparatus of claim 1 , wherein said second outlet and said third outlet lead to reservoirs where said enriched second and third flows, respectively, are collected.

11. The apparatus of claim 1 , wherein one or more surfaces of said separation regions are functionalized to interact physically or chemically with specific materials.

12. The apparatus of claim 1 , wherein said separation regions are constructed to align said plurality of components in a specific way.

13. The apparatus of claim 1 , further comprising a destruction region wherein one of said plurality of components are destroyed.

14. The apparatus of claim 1 , further comprising at least one of a sterilization region, a pressurization region, a temperature-controlled region, a mixing region, a bubble trap region, an electronic measurement region, a flow regulating mechanism, a pulsation suppression region, a diagnostic region, a flow leveling region, and a concentration measurement region.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 28, 2019
From: PREMIUM GENETICS (UK) LIMITED
To: ABS GLOBAL, INC.
Reel/Frame 050201/0345 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2013
From: ARRYX, INC.
To: PREMIUM GENETICS (UK) LIMITED
Reel/Frame 030914/0067 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 3, 2009
From: MUETH, DANIEL; SHIREMAN, JESSICA; ANDERSON, AMY
To: ARRYX, INC.
Reel/Frame 022502/0303 →
Continuity (3)
Division 1086732800 · Jun 13, 2004
Continuation In Part 1063090400 · Jul 31, 2003
Related Publication 20070114172A1 · May 24, 2007