IP Library Granted Patent US 9,086,371
Granted Patent B2
US 9,086,371 · App. 13/551,403 · Granted Jul 21, 2015

Fluidics devices

Inventors: Charles E Clemens (Encinitas, CA); Robert Mucic (Glendale, CA); Rudolph A. Montalvo (Woodland Hills, CA); Clark Foster (Mission Viejo, CA); Gary R. Gust (Huntington Beach, CA); Thomas P. Robinson (Encinitas, CA); Gary T. Olsen (La Crescenta, CA)
Assignee: OSMETECH TECHNOLOGY, INC.
G01N27/27B01L3/502715B01L3/502738B01L3/502707B01L3/502723B01L7/52B01L7/525B01L9/527B01L2200/025B01L2200/027B01L2200/0684B01L2200/10B01L2300/023B01L2300/024B01L2300/0636B01L2300/0645B01L2300/088B01L2300/0816B01L2300/0867B01L2300/0874B01L2300/0887B01L2300/123B01L2300/1827B01L2400/0439B01L2400/0442B01L2400/0478B01L2400/0481B01L2400/0487B01L2400/0605B01L2400/0655
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Quick Facts
Patent No.
US 9,086,371
App. No.
13/551,403
Granted
Jul 21, 2015
Kind
B2
Abstract

The invention relates to fluidics as used in medical and diagnostic equipment and relates further to means for purifying, abstracting, filtering, detecting and/or measuring analytes in liquid samples.

Claims (27)

1. A fluidics device comprising:

a flow channel for transporting a fluid sample;

an inlet port for receiving said fluid sample, said inlet port in fluid communication with a first bridge valve;

a diaphragm configured and adapted to interface with a pump, said diaphragm being coupled to said first bridge valve;

a second bridge valve in fluid communication with said flow channel, said second valve being coupled to said diaphragm,

wherein said diaphragm and said bridge valves are integral to a common membranous layer in a multilayer assembly, and

wherein each of said first bridge valve and said second bridge valves comprises a displaceable region between substantially parallel slits in the membranous layer, wherein the displaceable region allows said fluid sample to flow under or over said displaceable region according to a direction of displacement thereof.

2. The fluidics device of claim 1 , further comprising a working electrode located in said flow channel.

3. The fluidics device of claim 2 , further comprising an auxiliary electrode.

4. The fluidics device of claim 1 , further comprising a connector configured and adapted to interface with a detection device.

5. The fluidics device of claim 1 , further comprising an Electrically Erasable-Programmable Read-Only Memory (EEPROM).

6. The fluidics device of claim 1 , further comprising a binding partner or a ligand immobilized in said flow channel.

7. The fluidics device of claim 6 , wherein said binding partner or ligand is immobilized using a self-assembling monolayer that is affixed to an electrode surface.

8. The fluidics device of claim 6 , wherein said binding partner or ligand is selected from the group consisting of a polynucleotide, a protein, a peptide, an antibody, and a combination thereof.

9. The fluidics device of claim 1 , further comprising an array of electrodes, each bound to a binding partner or a ligand.

10. The fluidics device of claim 9 , wherein said electrode array comprises a plurality of different binding partners and/or ligands immobilized thereon.

11. The fluidics device of claim 9 , wherein said electrode array is located in a serpentine channel.

12. The fluidics device of claim 1 , wherein said flow channel comprises a cross-sectional dimension comprising a greater width than height.

13. The fluidics device of claim 1 , having a sample capacity ranging from about 50 μL to about 200 μL.

14. The fluidics device of claim 9 , having a single cartridge capacity of no more than about 200 μL, wherein said array is contained in a flow channel having a length ranging from about 100 mm to about 200 mm and a cross-sectional dimension ranging from about 0.75 mm to about 2.0 mm in width and about 0.125 mm to about 0.40 mm in height.

15. A diagnostic kit comprising the fluidics device of claim 1 .

16. A method of determining analyte binding, comprising:

providing the fluidics device according to claim 9 ;

adding to said device the fluid sample, wherein the fluid sample is suspected of containing an analyte specific for said binding partner or ligand;

circulating and recirculating said fluid sample across said electrode array; and

detecting binding of said analyte to said binding partner or ligand.

17. The method of claim 16 , wherein said circulating and recirculating is performed at a rate ranging from about 10 μL/sec to about 40 μL/sec.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 18, 2021
From: GENMARK DIAGNOSTICS, INC.
To: ROCHE MOLECULAR SYSTEMS, INC.
Reel/Frame 058189/0563 →
Continuity (5)
Continuation 12534681 · Aug 3, 2009
Division 12032356 · Feb 15, 2008
Provisional Application 60890180 · Feb 15, 2007
Provisional Application 60953197 · Jul 31, 2007
Related Publication 20130137591A1 · May 30, 2013