Device and method for carrying out fluoresence immunotests

• US 6,686,208 B2
• Filed: 08/06/2002
• Issued: 02/03/2004
• Est. Priority Date: 03/18/1997
• Status: Expired due to Fees

• Current Assignee: PES Gesellschaft Fur Medizinische Diagnose-Systeme MbH
• Original Assignee: Institut Fur Chemo- Und Biosensorik Munster e.V.
• Inventors: Katerkamp, Andreas, Meusel, Markus, Trau, Dieter
• Primary Examiner(s): Le, Long V.
• Assistant Examiner(s): Padmanabhan, Kartic
• Application Number:
  US10/212,954
• Publication Number:
  US 20030032199A1
• Time in Patent Office: 546 Days
• Field of Search: 333/210, 356/73.1, 356/129, 356/130, 356/246, 356/318, 356/337, 356/339, 356/340, 356/369, 356/445, 356/477, 356/481, 356/484, 356/517, 356/519, 356/521, 356/927, 356/928, 422/52, 422/57, 422/58, 422/60, 422/68.1, 422/82.08, 422/82.09, 422/82.11, 435/4, 435/7.1, 435/7.9, 435/7.92, 435/174, 435/177, 435/178, 435/179, 435/180, 435/287.1, 435/287.2, 435/287.9, 435/288.5, 435/808, 435/968, 435/969, 436/164, 436/170, 436/172, 436/518, 436/528, 436/529, 436/530, 436/805, 436/807
• US Class Current: 436/518
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: G01N 21/648 using evanescent coupling or surface plasmon coupling for the excitation of fluorescence
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: Y10S 435/808 Optical sensing apparatus
• CPC Class Codes: Y10S 435/968 High energy substrates, e.g. fluorescent, chemiluminescent, radioactive
• CPC Class Codes: Y10S 435/969 Multiple layering of reactants
• CPC Class Codes: Y10S 436/805 Optical property
• CPC Class Codes: Y10S 436/807 Apparatus included in process claim, e.g. physical support structures

Abstract

The invention relates to devices and methods for carrying out quantitative fluorescence immunoassays using evanescent field excitation. Light from at least one light source is directed onto the boundary between two media which have differing refractive indices. The light source emits practically monochromatic light with a wavelength suitable for exciting a marking substance. The light is directed onto a boundary surface disposed between an optically transparent base plate, the refractive index of which is greater than that of the material above the boundary surface, and a receiving region for the sample. The receiving region is covered with a covering plate on the side disposed opposite the base plate, there being arranged between the base plate and covering plate at least one functional layer. A detector for detecting the fluorescent light is disposed on the same side of the base plate as the light source.

Claims

1. A device for carrying out fluorescence immunoassays by means of evanescent field excitation, the device comprising:

an optically transparent base plate;

a receiving region for a sample;

a boundary surface between the base plate and the receiving region, the base plate having a refractive index greater than that of a material above the boundary surface;

a plate covering the receiving region on a side opposite the base plate;

a functional layer between the base plate and covering plate or in an inflow region for the sample into the receiving region, flowed through laterally or transversally by means of suction, pressure, or capillary force;

a light source, emitting practically monochromatic light, directing light rays with a wavelength causing fluorescence of a marking substance bound to a chemical or biochemical partner of a receptor-ligand system onto the boundary surface on a side of the base plate opposite the covering plate; and

a fluorescence detector disposed on the side of the base plate opposite the covering plate, the fluorescence detector disposed to detect fluorescence passing through the base plate and then passing through air to the fluorescence detector, the fluorescence detector not disposed to detect fluorescence coupled into the base plate acting as a waveguide.

2. The device according to claim 1, further comprising:

a spacer between the base plate and covering plate forming the receiving region.

3. The device according to claim 1, further comprising:

an inlet aperture and an outlet aperture in the covering plate.

4. The device according to claim 3, wherein a plurality of functional layers, separated by separating layers, are disposed alternating one above another, making possible a connection of the inlet and outlet apertures via the receiving region by means of openings.

5. The device according to claim 4, wherein at least two different functional layers are disposed beside one another in one plane.

6. The device according to claim 1, wherein the functional layer consists of fibrous material, cellulose, nitrocellulose, polypropylene, poly-carbonate, polyvinyl difluoride, or of a hydrogel, or of polyelectrolytes, or of track-etch membrane or glass fibre membranes, or is configured as a packed column.

7. The device according to claim 1, wherein at least one functional layer in the receiving region is in direct contact with the base plate.

8. The device according to claim 1, wherein a plurality of functional layers are disposed one directly above another.

9. The device according to claim 1, further comprising:

a sample container that defines a sample volume, the sample container so disposed that a formed between the receiving region and sample container.

10. The device according to claim 9, wherein a solid phase is formed in the sample container, in an inflow region, in the receiving region, or as a functional layer.

11. A method of carrying out fluorescence immunoassays by means of evanescent field excitation, the method comprising:

guiding a sample volume by means of suction, pressure, or by capillary forces, through at least one functional layer and thereafter through a receiving region;

emitting light with a wavelength causing fluorescence of marked chemical or biochemical components bound to a surface in the receiving region; and

measuring fluorescence with a detector, the detector disposed to detect fluorescence passing through a base plate adjoining the receiving region and then passing through air to the detector, the detector not disposed to detect fluorescence coupled into the base plate acting as a waveguide.

12. The method according to claim 11, wherein the at least one functional layer carries out a function from the group consisting of filtration, separation, elimination of interfering substances, and release of reagents.

13. The method according to claim 11, wherein a rise in a measured fluorescent light intensity correlates with and is used to determine an analyte concentration.

14. The method according to claim 11, wherein a difference between two fluorescence intensity signals, measured in intervals, is used to determine an analyte concentration.

15. The method according to claim 11, wherein with the sample volume is carried out a biochemical assay of a receptor-ligand system selected from the group consisting of:

antigen-antibody, lectin-carbohydrate, DNA-complementary nucleic acid, RNA-complementary nucleic acid, DNA-protein, RNA-protein, hormone-receptor, enzyme—

enzyme cofactors, protein G-immunoglobin, protein A-immunoglobin, and avidin-biotin.

16. The method according to claim 11, wherein a sandwich assay is carried out by:

leading an analyte into the receiving region, at least some of the analyte binding to the bound chemical or biochemical components; and

leading a marked antibody into the receiving region, at least some of the marked antibody binding to the analyte, wherein there is a direct correlation between an amount of measured fluorescent light and a concentration of the analyte in the receiving region.

17. The method according to claim 11, in which a competition assay is carried out by:

leading an analyte into the receiving region, at least some of the analyte binding to the bound chemical or biochemical components; and

leading a marked test compound into the receiving region, at least some of the marked test compound binding to the bound chemical or biochemical components, wherein there is an inverse correlation between an amount of measured fluorescent light and a concentration of the analyte in the receiving region.