IP Library Granted Patent US 9,903,799
Granted Patent B2
US 9,903,799 · App. 15/493,061 · Granted Feb 27, 2018

Whole blood analytic device and method therefor

Inventors: Michael Poirier (Vista, CA); John Stephen Middleton (Carlsbad, CA); Suzanne Marie Poirier (Vista, CA)
Assignee: Qualigen, Inc.
G01N1/4005B01D69/02G01N33/491B01D2319/06B01D2325/36B01D2325/38
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Quick Facts
Patent No.
US 9,903,799
App. No.
15/493,061
Granted
Feb 27, 2018
Kind
B2
Abstract

Devices and methods are presented in which a plasma separation device with a first and second portion separates a blood containing fluid. Most preferably, the first portion produces a cell fraction and a plasma fraction, and the second portion captures the plasma fraction. A first actuator then fluidly isolates a portion of the plasma fraction within the second portion, and a second actuator moves the isolated portion of the plasma fraction from the second portion.

Claims (35)

1. An analytic device, comprising:

a sample receiving compartment;

a plasma separation device that is at least partially disposed in the sample receiving compartment and comprises (1) a first portion configured to separate blood into a cell fraction and a plasma fraction, and (2) a second portion configured to capture at least a portion of the plasma fraction;

wherein the analytic device comprises a flexible first area that, when compressed by a first actuator, exerts pressure on a first part of the second portion and thereby restricts flow of the plasma fraction between the first and the second portion;

wherein the analytic device has a third flexible area that is fluidly coupled to the sample receiving compartment and that, when compressed by a third actuator, allows for flow of a reagent from the third flexible area to a second part of the second portion to thereby mix the reagent with the plasma fraction in the second part of the second portion; and

wherein the analytic device has a flexible second area that, when compressed by a second actuator, allows for flow of the mixture out of the sample receiving compartment.

2. The device of claim 1 , wherein the first portion comprises a hydrophobic separation membrane.

3. The device of claim 1 , wherein the second portion comprises a hydrophilic membrane having a void volume for collection of a predetermined volume of plasma.

4. The device of claim 1 , wherein the first and second portions are fluidly coupled to each other to allow capillary flow of the plasma fraction from the first portion to the second portion.

5. The device of claim 1 , wherein the flexible first area is formed from a flexible wall of the analytic device.

6. The device of claim 1 , wherein the first actuator is configured as a knife edge.

7. The device of claim 1 , wherein the flexible second area is formed from a flexible wall of the analytic device.

8. The device of claim 1 , wherein the analytic device is configured to allow bidirectional flow of the mixture between the sample receiving compartment and the third flexible area.

9. The device of claim 1 , wherein the analytic device is configured as a pouch having multiple compartments that are fluidly coupled to each other.

10. A method of manipulating a sample for a diagnostic test, comprising:

contacting a plasma separation device with a blood-containing fluid, wherein the plasma separation device has a first portion and a second portion;

using the first portion to separate the blood-containing fluid into a cell fraction and a plasma fraction, and using the second portion to capture the plasma fraction;

using a first actuator to fluidly isolate a portion of the plasma fraction within the second portion by applying pressure to a first part of the second portion;

using a third actuator to move a reagent to the isolated portion of the plasma fraction to form a mixture between the reagent and the isolated portion of the plasma fraction while the first actuator compresses the one part of the second portion; and

using a second actuator to move the mixture away from the second portion by applying pressure to a second part of the second portion while the first actuator compresses the one part of the second portion.

11. The method of claim 10 , wherein the plasma separation device is at least partially disposed within a container.

12. The method of claim 10 , wherein separation of the blood-containing fluid is driven by capillary action.

13. The method of claim 10 , wherein the first actuator has a knife edge that applies pressure to the one part of the second portion of the plasma separation device.

14. The method of claim 10 , wherein the first, second, and third actuators apply pressure to respective first, second, and third flexible portions of a pouch having multiple compartments that are fluidly coupled to each other.

15. The method of claim 10 further comprising a step of reacting a component in the plasma fraction with the reagent while the plasma fraction is in the second portion.

16. The method of claim 15 generating a signal from the reaction and measuring the signal.

17. A method of manipulating a sample for a diagnostic test, comprising:

using capillary force in a plasma separation device to separate a blood-containing fluid into a cell fraction and a plasma fraction;

receiving and retaining at least some of the plasma fraction in a membrane;

applying pressure to a first portion of the membrane to thereby fluidly isolate a portion of the plasma fraction within a second portion of the membrane, wherein the second portion of the membrane provides a predetermined sample volume;

moving a reagent to the isolated portion of the plasma fraction to form a mixture between the reagent and the isolated portion of the plasma fraction while maintaining pressure to the first portion of the membrane; and

applying pressure to the mixture while maintaining pressure to the first portion of the membrane to thereby move the mixture away from the second portion of the membrane.

18. The method of claim 17 , wherein the membrane is disposed within a sample receiving compartment and coupled to a hydrophobic separation membrane that is disposed outside the sample receiving compartment.

19. The method of claim 17 , wherein at least one of the steps of compressing the first and the second portion is performed through a flexible wall of a container.

20. The method of claim 17 , further comprising a step of reacting a component in the plasma fraction with the reagent while the plasma fraction is in the second portion.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Dec 2, 2020
From: SEKISUI DIAGNOSTICS, LLC
To: QUALIGEN, INC.
Reel/Frame 054521/0829 →
SECURITY INTEREST Recorded Jun 12, 2019
From: QUALIGEN, INC.
To: SEKISUI DIAGNOSTICS, LLC
Reel/Frame 049444/0663 →
SECURITY INTEREST Recorded Mar 19, 2018
From: QUALIGEN, INC.
To: SEKISUI DIAGNOSTICS LLC
Reel/Frame 045274/0593 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2017
From: POIRIER, MICHAEL; MIDDLETON, JOHN STEPHEN; POIRIER, SUZANNE MARIE
To: QUALIGEN, INC.
Reel/Frame 042087/0293 →
Continuity (2)
Division 14398409
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