Indicator immobilization on assay devices

• US 7,935,538 B2
• Filed: 12/15/2006
• Issued: 05/03/2011
• Est. Priority Date: 12/15/2006
• Status: Active Grant

• Current Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Original Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Inventors: Sayre, Curtis, Feaster, Shawn R., Villanueva, Julie, Song, Xuedong
• Primary Examiner(s): NGUYEN, BAO THUY L
• Application Number:
  US11/640,100
• Publication Number:
  US 20080145949A1
• Time in Patent Office: 1,600 Days
• Field of Search: 422/50, 422/55, 422/56, 422/68.1, 435/4, 435/287.1, 435/288.7, 436/518, 436/528
• US Class Current: 436/514
• CPC Class Codes: G01N 21/78 producing a change of colour
• CPC Class Codes: G01N 33/54388 based on lateral flow
• CPC Class Codes: G01N 33/54393 Improving reaction conditions or stability, e.g. by coating or irradiation of surface, by reduction of non-specific binding, by promotion of specific binding
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387
• CPC Class Codes: Y10S 435/97 Test strip or test slide
• CPC Class Codes: Y10S 436/81 Tube, bottle, or dipstick

Abstract

A lateral flow assay device for detecting the presence or quantity of an analyte in a test sample is provided. The device comprises a chromatographic medium that defines a detection zone, wherein a crosslinked network is non-diffusively immobilized within the detection zone. The crosslinked network contains a small molecule indicator that is configured to undergo a detectable color change in the presence of the analyte.

Claims

1. A lateral flow assay device for detecting the presence or quantity of an analyte in a test sample comprising a chromatographic medium that includes a conjugate pad located upstream of a detection zone, wherein a crosslinked network is non-diffusively immobilized within the detection zone, the crosslinked network containing a plurality of small molecule indicators that are configured to undergo a detectable color change in the presence of the analyte, the small molecule indicators of the crosslinked network being crosslinked to one another either directly or via a crosslinking agent that binds the small molecule indicators, the crosslinked network further comprising an anchoring compound that links the chromatographic medium and one of the plurality of small molecular indicators of the crosslinked network.

2. The lateral flow assay device of claim 1, wherein the small molecule indicator is covalently bound to the anchoring compound.

3. The lateral flow assay device of claim 1, wherein the small molecule indicator is bound to the anchoring compound via charge-charge interactions.

4. The lateral flow assay device of claim 1, wherein the anchoring compound is covalently bound to the chromatographic medium.

5. The lateral flow assay device of claim 1, wherein the anchoring compound is bound to the chromatographic medium via charge-charge interactions.

6. The lateral flow assay device of claim 1, wherein the anchoring compound is a macromolecular compound.

7. The lateral flow assay device of claim 6, wherein the macromolecular anchoring compound is a polymer.

8. The lateral flow assay device of claim 1, wherein the small molecule indicators include a diazonium compound.

9. The lateral flow assay device of claim 1, wherein the small molecule indicators include a benzidine compound, phthalein compound, aminobenzaldehyde compound, or a combination thereof.

10. The lateral flow assay device of claim 1, further comprising an enzyme substrate contained within the conjugate pad.

11. The lateral flow assay device of claim 1, further comprising a control zone.

12. The lateral flow assay device of claim 1, further comprising detectable reagents in fluid communication with the chromatographic medium.

13. The lateral flow assay device of claim 1, wherein the crosslinked network is formed with electromagnetic radiation.

14. The lateral flow assay device of claim 13, wherein the radiation is ultraviolet radiation.

15. The lateral flow assay device of claim 1, wherein the crosslinked network is formed with thermal energy.