Electrophoretic bar code assay devices and methods for making and using the same

Patent metadata

Field	Value
Publication number	US-10634673-B2
Application number	US-201314440852-A
Country	US
Kind code	B2
Filing date	Nov 11, 2013
Priority date	Nov 12, 2012
Publication date	Apr 28, 2020
Grant date	Apr 28, 2020

Abstract

A microfluidic device for determining whether an analyte is present in a sample is provided. The microfluidic device includes an elongated flow path having a polymeric medium, where the polymeric medium includes a first analyte detection domain having a first immobilized capture member that specifically binds to a first analyte and a second analyte detection domain having a second immobilized capture member that specifically binds to a second analyte. Also provided are methods, systems and kits in which the subject microfluidic devices find use, as well as methods of producing the same.

First claim

That which is claimed is:

1. An assay device comprising:
a microchannel comprising a polymeric medium, wherein the polymeric medium comprises:
a first analyte detection domain, wherein the first analyte detection domain comprises a first immobilized capture member that specifically binds to a first analyte;
a second analyte detection domain, wherein the second analyte domain comprises a second immobilized capture member that specifically binds to a second analyte; and
a spacer domain disposed between the first analyte detection domain and the second analyte detection domain, wherein the spacer domain comprises a first member of a specific binding member pair bound to a second member of the specific binding member pair, wherein the second member of the specific binding member pair is not bound to a capture member, wherein the first member and the second member do not bind to the first analyte or the second analyte,
wherein the first member of the specific member binding pair is coupled to the polymeric medium throughout the entire polymeric medium,
wherein the first immobilized capture member and the second immobilized capture member are immobilized to the polymeric medium through the first member.

2. The assay device according to claim 1 , wherein the polymeric medium comprises a polymeric gel.

3. The assay device according to claim 1 , wherein the first immobilized capture member is bound to the polymeric medium in the first analyte detection domain.

4. The assay device according to claim 3 , wherein the first immobilized capture member is non-covalent bound to the polymeric medium in the first analyte detection domain via a specific binding member pair.

5. The assay device according to claim 4 , wherein the specific binding member pair comprises biotin and streptavidin.

6. The assay device according to claim 5 , wherein the first immobilized capture member comprises streptavidin bound to the polymeric medium and biotin bound to a ligand of the first analyte.

7. The assay device according to claim 1 , wherein the second immobilized capture member is bound to the polymeric medium in the second analyte detection domain.

8. The assay device according to claim 7 , wherein the second immobilized capture member is non-covalently bound to the polymeric medium in the second analyte detection domain via a specific binding member pair.

9. The assay device according to claim 8 , wherein the specific binding member pair comprises biotin and streptavidin.

10. The assay device according to claim 9 , wherein the second immobilized capture member comprises streptavidin bound to the polymeric medium and biotin bound to a ligand of the second analyte.

11. A method of determining whether an analyte is present in a sample, the method comprising:
introducing a sample into a microchannel comprising a polymeric medium, wherein the polymeric medium comprises:
a first analyte domain comprising a first immobilized capture member that specifically binds to a first analyte;
a second analyte domain comprising a second immobilized capture member that specifically binds to a second analyte; and
a spacer domain disposed between the first analyte detection domain and the second analyte detection domain, wherein the spacer domain comprises a first member of a specific binding member pair bound to a second member of the specific binding member pair, wherein the second member of the specific binding member pair is not bound to a capture member, wherein the first member and the second member do not bind to the first analyte or the second analyte,
wherein the first member of the specific member binding pair is coupled to the polymeric medium throughout the entire polymeric medium,
wherein the first immobilized capture member and the second immobilized capture member are immobilized to the polymeric medium through the first member;

applying a directional electric field to the microchannel in a manner sufficient to move components through the polymeric medium; and
obtaining a signal from the first analyte detection domain and the second analyte detection domain to determine whether the first analyte and the second analyte are present in the sample.

12. The method according to claim 11 , comprising labeling the sample prior to introducing the sample into the microchannel.

13. The method according to claim 11 , comprising introducing a label into the elongated flow path after the sample is introduced into the microchannel.

14. The method according to claim 13 , wherein the label is a detectable label.

15. The method according to claim 14 , wherein the detectable label comprises a fluorescent moiety.

16. The method according to claim 11 , wherein the analyte is selected from a protein, a peptide, an antibody, a diabody, a Fab fragment, a DNA binding protein, an RNA binding protein, a phosphorylated protein, a peptide aptamer, and an epitope.

17. The method according to claim 11 , wherein the sample comprises urine, blood, serum, plasma, saliva, semen, prostatic fluid, nipple aspirate fluid, lachrymal fluid, perspiration, feces, cheek swabs, cerebrospinal fluid, cell lysate samples, amniotic fluid, gastrointestinal fluid, biopsy tissue, or a sample obtained from laser capture microdissection (LCM).

18. A system for assaying a fluid sample for the presence of two or more analytes, the system comprising:
(a) an assay device according to claim 1 ; and
(b) a detector.

19. The system according to claim 18 , further comprising components configured to direct a fluid through the assay device.

20. A kit comprising:
(a) an assay device according to claim 1 ; and
(b) a packaging configured to contain the assay device.

21. A method of producing an assay device, the method comprising:
producing a precursor polymeric medium in a microchannel, wherein the precursor polymeric medium comprises a first member of a specific binding pair coupled to the polymeric medium throughout the entire polymeric medium;
introducing into the microchannel a defined amount of a first capture member bound to a second member of the specific binding pair in a manner sufficient to produce a first analyte detection domain that comprises a first immobilized capture member that specifically binds to a first analyte in the microchannel, wherein the first immobilization capture member is immobilized to the polymeric medium through the first member;
introducing into the microchannel a defined amount of the second member of the specific binding pair in a manner sufficient to produce a spacer domain,
wherein the spacer domain comprises the first member of the specific binding member pair bound to the second member of the specific binding member pair, wherein the second member of the specific binding member pair is not bound to a capture member;

and
introducing into the microchannel a defined amount of a second capture member bound to the second member of the specific binding pair in a manner sufficient to produce a second analyte detection domain that comprises a second immobilized capture member that specifically binds to a second analyte in the microchannel, wherein the second immobilization capture member is Immobilized to the polymeric medium through the first member;
wherein the spacer domain is disposed between the first analyte detection domain and the second analyte detection domain, wherein the first member and the second member do not bind to the first analyte or the second analyte
to produce the assay device.

22. The

Assignees

• Univ California

Inventors

• Araz M Kursad
• Apori Akwasi A
• Herr Amy E

Classifications

• B01L2300/0825

  Test strips · CPC title

• B01L2300/0636

  Integrated biosensor, microarrays · CPC title

• B01L2400/0421

  electrophoretic flow · CPC title

• G01N33/54366

  Apparatus specially adapted for solid-phase testing · CPC title

• B01L2400/0415

  electrical forces, e.g. electrokinetic · CPC title