Photoelectrochemical immunoassay

• US 4,293,310 A
• Filed: 03/14/1980
• Issued: 10/06/1981
• Est. Priority Date: 03/14/1980
• Status: Expired due to Term

• Current Assignee: University Of Pittsburgh (University of Pittsburgh of The Commonwealth System of Higher Education)
• Original Assignee: University Of Pittsburgh (University of Pittsburgh of The Commonwealth System of Higher Education)
• Inventors: Weber, Stephen G.
• Primary Examiner(s): Marantz, Sidney
• Application Number:
  US06/130,555
• Time in Patent Office: 571 Days
• Field of Search: 23/230 B, 23/915, 424/8, 424/12, 204/195 B, 422/68
• US Class Current: 436/536
• CPC Class Codes: G01N 33/532 Production of labelled immunochemicals
• CPC Class Codes: G01N 33/533 with fluorescent label
• CPC Class Codes: G01N 33/5438 Electrodes
• CPC Class Codes: G01N 33/58 involving labelled substances G01N33/53 takes precedence
• CPC Class Codes: Y10S 436/805 Optical property
• CPC Class Codes: Y10S 436/807 Apparatus included in process claim, e.g. physical support structures
• CPC Class Codes: Y10S 436/816 Alkaloids, amphetamines, and barbiturates
• CPC Class Codes: Y10S 436/817 Steroids or hormones

Abstract

A method and apparatus for the determination of trace amounts of chemicals in a system, as for example the immunoassay determination of hormones, peptides and drugs in biological fluids, applies photoelectrochemistry to the field of immunoassay. The apparatus and method comprise a photoelectrochemically active molecule as a label in an immunoassay system of labeled analyte, antibody sensitive to analyte, quencher and an electrochemical flow cell with light means. The photoelectrochemically active molecule upon photoexcitation transfers an electron to a quencher molecule; the oxidized molecule is subsequently reduced with an electron from an electrode of the flow cell which is held at suitable potential. This electron is measured as photocurrent. The electrochemical flow cell is channeled for the flow of solution containing photoelectrochemically active species and quencher; and has at least one wall transparent to light such as a laser which is trained on the appropriate region of the cell; and further comprises means to isolate the spectral region of interest and means to distinguish photocurrent from nonphotocurrent. The amount of free labeled analyte in the system is determined by the photocurrent signal.

Claims

1. Immunoassay apparatus comprising:

(i) a catalytic photoelectrochemical label capable of photoexcitation such that a photocurrent is generated at an electrode of appropriate potential;

(ii) a quencher; and

(iii) an electrochemical flow cell having,

at least one wall transparent to light of a spectrum which will excite said photoelectrochemically active label, and

(iv) light means which further comprise,

a light source having a spectrum capable of exciting said photoelectrochemically active label, and means for isolating said spectrum, wherein the relative planes of orientation of the electrodes of said cell, and said spectrum are disposed such that said photoelectrochemically active label will react with said quencher to generate said photocurrent, and

means for distinguishing between said photocurrent and non-photocurrent.

2. The detecting apparatus of claim 1 wherein said photoelectrochemically active label is a ruthenium complex.

3. The detecting apparatus of claim 2 wherein said ruthenium complex is RuL₃ and L is a derivative of o-phenanthroline or 2,2'"'"'-bipyridine or combination thereof.

4. The detecting apparatus of claim 3 wherein said RuL₃ is tris (2,2'"'"'-bipyridyl) ruthenium (ii).

5. The detecting apparatus of claim 1 wherein said photoelectrochemically active label is an osmium complex.

6. The detecting apparatus of claim 5 wherein said osmium complex is OsL₃ and L₃ is a derivative of o-phenanthroline or 2,2'"'"'-bipyridine or combinations thereof.

7. The detecting apparatus of claim 1 wherein said quencher is Co(C₂ O₄)₃^3-.

8. The detecting apparatus of claim 1 wherein said quencher is hydrazine.

9. The detecting apparatus of claim 1 wherein said light source is a hollow cathode lamp.

10. The detecting apparatus of claim 9 wherein said cathode is a strontium lamp.

11. The detecting apparatus of claim 1 wherein said light source is a Xe arc lamp.

12. The detecting apparatus of claim 1 wherein said light source is a laser.

13. The detecting apparatus of claim 1 wherein said means for distinguishing between said photocurrent and non-photocurrent further comprises a light beam chopper, filters, lenses and lock-in amplifier.

14. The detecting apparatus of claim 1 wherein said means for distinguishing between said photocurrent and non-photocurrent further comprises a first working electrode exposed to said light and a second working electrode in the dark, such that the difference in current signals is the signal due to the presence of light.

15. The detecting apparatus of claim 1 wherein said isolated spectrum is in one range at 430-500 nm.

16. The detecting apparatus of claim 14 wherein said means for isolating said spectrum further comprises a monochromater.

17. The detecting apparatus of claim 1 wherein said relative planes of orientation are disposed such that said spectrum impinges perpendicularly to said electrodes.

18. The detecting apparatus of claim 1 wherein said relative planes of orientation are such that said spectrum impinges parallel to said electrodes.

19. A catalytic photoelectrochemical method of immunoassay comprising the steps of:

(i) utilizing a photoelectrochemically labeled antigen and quencher in an assay of analyte, labeled analyte and antibody specific to said analyte, and

(ii) measuring the concentration of said photoelectrochemically labeled analyte with an electrochemical flow cell, having means for distinguishing photocurrent and non-photocurrent;

light means which further comprises a light source, having a spectrum capable of exciting said photoelectrochemically active label, and means for isolating said spectrum, wherein the relative planes of orientation of the electrodes of said cell, and said spectrum are disposed such that said photoelectrochemically active label will react with said quencher to generate said photocurrent.

20. A catalytic photochemical method of immunoassay comprising the steps of:

(i) utilizing a photoelectrochemical as a label with a labeled analyte, and a quencher, in an assay mixture of analyte, labeled analyte and antibodies specific to said analyte, and

(ii) measuring the concentration of said photoelectrochemically labeled analyte with an electrochemical flow cell, having,

at least one wall transparent to light of a spectrum which will excite said photoelectrochemically active label, means for distinguishing between said photocurrent and nonphotocurrent and

light means which further comprises,

a light source having a spectrum capable of exciting said photoelectrochemically active label, and means for isolating said spectrum, wherein the relative planes of orientation of the electrodes of said cell, as a spectrum are disposed such that said photoelectrochemically active label will react with said quencher to generate said photocurrent.