ELECTRONIC ANALYTE ASSAYING DEVICE

• US 20100240149A1
• Filed: 06/03/2010
• Published: 09/23/2010
• Est. Priority Date: 07/09/2004
• Status: Active Grant

• Current Assignee: Church & Dwight Company Incorporated
• Original Assignee: Church & Dwight Company Incorporated
• Inventors: Nazareth, Albert R., Delahanty, Francis T., Bandru, Gregory M., Synakowski, Stephen R., Wieck, Henry J.
• Granted Patent: US 8,623,635 B2
• Time in Patent Office: Days
• US Class Current: 436/501
• CPC Class Codes: G01N 21/8483 Investigating reagent band test-element handling not specific to a test method G01N33/4875; analytical elements specific to chemical analysis of biological material G01N33/52; autometer with reagent band G01N35/04
• CPC Class Codes: G01N 33/5302 Apparatus specially adapted for immunological test procedures
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387
• CPC Class Codes: G01N 33/689 related to pregnancy or the gonads

Abstract

The invention is an electronically processed single-step test device for detecting the presence of a preselected analyte in a fluid. The device includes a hollow rectangular outer casing, disposed within co-joined upper and lower sections of the casing are assay material, an electronic processing system, and a LCD display. The LCD display is observable through a viewing window. The assay material is a sorptive material including a fluid sample application region in the form of a sample wick in fluid communication with a test strip. The test strip includes an analyte capture region adjacent to a light shield. The electronic processing system includes red and green LEDs which are alternately pulsed or energized over predetermined periods of time to determine if fluid test results show a marker or markers in the capture region indicative of the presence of a preselected analyte in the fluid. If so, Yes+ is displayed on the LCD. If not, No− is displayed on the LCD.

Claims

1. A diagnostic device for detecting the presence of an analyte in a fluid sample, the device comprising:

a. a casing having a display;

b. a lateral flow diagnostic strip having a first end and an opposite second end, wherein at least a portion of said lateral flow diagnostic strip is received in said casing and said lateral flow diagnostic strip first end is configured to receive a fluid sample, said lateral flow diagnostic strip having

(i) a capture region intermediate said lateral flow diagnostic strip first and second ends,

(ii) a labeled conjugate comprising a first binding member, configured to be reactive with a first epitope of the analyte in the fluid sample and a detectable label, located proximate said lateral flow diagnostic strip first end,

(iii) a capturable component comprising of a second binding member configured to be reactive with a second epitope of the analyte located intermediate said labeled conjugate and said capture region, and

(iv) a capture component located at said lateral flow diagnostic strip capture region,

c. a processor received in said casing;

d. at least one light source received in said casing and operatively coupled to said processor;

e. at least one sensor received in said casing and operatively coupled to said processor, said at least one sensor positioned proximate said lateral flow diagnostic strip so as to sense said capture region;

wherein

when the fluid sample is received at said lateral flow diagnostic strip first end said labeled conjugate is reconstituted in the sample fluid;

the fluid sample and said reconstituted labeled conjugate move toward said capture region;

said at least one light source, said at least one sensor and said processor are configured to detect a valid fluid front by detecting a presence of said labeled conjugate in the fluid sample as it passes said capture region prior to detecting the presence of the analyte.

2. The device of claim 1, wherein said first binding member comprises a first monoclonal antibody.

3. The device of claim 1, wherein said detectable label is colloidal gold particles.

4. The device of claim 1, wherein said capturable component is biotin conjugated to monoclonal antibody.

5. The device of claim 1, wherein said capture component is avidin.

6. The device of claim 1, further comprising a display operatively coupled to said processor, wherein said processor is configured to present a message on said display if said valid fluid front is not detected.

7. The device of claim 1, wherein said processor is configured to

(i) turn said at least one light source on and activate said at least one sensor to capture data at said capture zone at a first time;

(ii) turn said at least one light source on and activate said at least one sensor to capture data at said capture zone at a second time; and

(iii) compare said first captured data with said second captured data to determine if said valid fluid front is present by detecting the presence of said detectable labeled conjugate.

8. The device of claim 1, further comprising a sample receiving member coupled to said lateral flow diagnostic strip first end for delivering the urine sample to said lateral flow diagnostic strip first end.

9. The device of claim 1, wherein

a. said at least one light source is a light emitting diode;

and

b. said at least one sensor is a photo detector.

10. The device of claim 1, wherein said processor is a software driven processor.

11. The device of claim 1, wherein said processor is a state machine.

12. A diagnostic device for detecting the presence of an analyte in a fluid sample, the device comprising:

a. a casing having a display;

b. a lateral flow diagnostic strip having a first end and an opposite second end, wherein said lateral flow diagnostic strip is received in said casing and said lateral flow diagnostic strip first end is configured to receive a fluid sample, said lateral flow diagnostic strip having a capture region intermediate said lateral flow diagnostic strip first and second ends;

c. a processor received in said casing;

d. at least one light source mounted in said casing and operatively coupled to said processor;

e. at least one sensor mounted in said casing and operatively coupled to said processor, said at least one sensor positioned proximate said lateral flow diagnostic strip so as to sense said capture region;

wherein

when the fluid sample is received at said lateral flow diagnostic strip first end said detectable labeled conjugate is reconstituted in the sample fluid and moves laterally along said lateral flow diagnostic strip toward said capture region, and

said at least one light source, said at least one sensor and said processor are configured to detect a valid fluid front by detecting a presence of said detectable labeled conjugate in the fluid sample as it passes said capture region.

13. The device of claim 12, said lateral flow diagnostic strip further comprising:

a. a labeled conjugate comprising of a first binding member, configured to be reactive with a first epitope of the analyte in the fluid sample, and a detectable label located proximate said lateral flow diagnostic strip first end,

b. a first capturable component comprising a second binding member configured to be reactive with a second epitope of the analyte located intermediate said first binding member and said capture region, and

c. a capture component located at said lateral flow diagnostic strip capture region.

14. The device of claim 12, wherein said first binding member comprises a first monoclonal antibody.

15. The device of claim 12, wherein said detectable label is colloidal gold particles.

16. The device of claim 12, wherein said capturable component is biotin conjugated to a monoclonal antibody.

17. The device of claim 12, wherein said capture component is avidin.

18. The device of claim 12, wherein said processor is a software driven processor.

19. The device of claim 12, wherein said processor is a state machine.

20. A method of detecting a valid fluid front in a diagnostic device for detecting the presence of an analyte in a fluid sample, said method comprising:

a. providing

(i) a lateral flow diagnostic strip having a first end configured to receive a fluid sample, said lateral flow diagnostic strip having a capture region and a detectable labeled conjugate proximate said first end,

(ii) a processor,

(iii) at least one light source operatively coupled to said processor and positioned proximate said lateral flow diagnostic strip capture region, and

(iv) at least one sensor operatively coupled to said processor and positioned proximate said lateral flow diagnostic strip capture region;

b. illuminating said lateral flow diagnostic strip capture region with said at least one light source;

c. electronically sensing said lateral flow diagnostic strip capture region with said at least one sensor at a first and a second predetermined time;

d. electronically detecting the presence of a valid fluid front by detecting the presence of said detectable labeled conjugate prior to detecting the presence of the analyte to determine whether the lateral flow diagnostic strip is operating correctly.

21. The method of detecting a valid fluid front in a diagnostic device of claim 20, wherein

a. said at least one light source is a light emitting diode;

and

b. said at least one sensor is a photo detector.

22. The method of detecting a valid fluid front in a diagnostic device of claim 20, wherein the step of detecting the presence of said detectable labeled conjugate further comprises

a. subtracting the a sensed signal at said second predetermined time from a sensed signal at said first predetermined time;

and

b. determining whether said result is greater than a predetermined threshold value.

23. The method of detecting a valid fluid front in a diagnostic device of claim 20, further comprising the step of electronically displaying an error message if said valid fluid front is not detected within a predetermined time.