Apparatus including optical fiber for fluorescence immunoassay

• US 4,582,809 A
• Filed: 08/09/1982
• Issued: 04/15/1986
• Est. Priority Date: 06/14/1982
• Status: Expired due to Term

• Current Assignee: Roche Diagnostics Corporation (Roche Holding AG)
• Original Assignee: Myron J. Block
• Inventors: Block, Myron J., Hirschfeld, Tomas B.
• Primary Examiner(s): Marantz, Sidney
• Application Number:
  US06/406,324
• Time in Patent Office: 1,345 Days
• Field of Search: 436/527, 436/805, 436/172, 422/56, 422/57, 422/68, 250/227, 250/302, 250/365, 356/73.1, 356/445
• US Class Current: 436/527
• CPC Class Codes: G01N 2021/7786 Fluorescence
• 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 21/7703 using reagent-clad optical fibres or optical waveguides using measurement of total internal reflection or attenuated total reflection G01N21/552; optical fibres or waveguides per se G02B
• CPC Class Codes: Y10S 436/805 Optical property

Abstract

A method and apparatus for fluorescent immunoassay utilizes total internal reflection at the interface between a solid phase and a liquid phase of lower index of refraction to produce an evanescent wave in the liquid phase. The solid phase is arranged and illuminated so as to provide multiple total internal reflections at the interface. In a preferred embodiment, the solid phase is in the form of an optical fiber to which is immobilized a component of the complex formed in the immunochemical reaction. A fluorophore is attached to another component of the complex. The fluorescent labelled component may be either the complement to or an analog of the immobilized component, depending on whether competitive or sandwich assays are to be performed. In the case of competitive assays, the labelled component is preferably pre-loaded to the immobilized component in a controlled concentration. The fiber (and the attached constituent of the assay) is immersed in the liquid phase sample. The evanescent wave is used to excite fluorescence in the liquid phase, and that fluorescence which tunnels back into the solid phase and accumulates during multiple reflections while channeled in the solid phase is detected. Diffusional preconcentration onto the reactive surface and double passing enhance the signal and signal/background ratio.

Claims

1. Apparatus for fluorescence immunoassays relying on an immunochemical complex formed by reaction between a first constituent of said immunochemical complex and a second constituent of said immunochemical complex, which second constituent includes a fluorescent tag, said apparatus comprising in combination:

an optical fiber transmissive to radiation which can excite fluorescene of said fluorescent tag and transmissive to fluorescent radiation from said fluorescent tag; and

a plurality of said first constituents so attached to at least a portion of the side surface of said optical fiber as to leave substantially unaffected the reactivity of said first constituent to form said immunochemical complex, with at least a part of said first constituent being complexed with a predetermined amount of said second constituent.

2. Apparatus for fluorescence immunoassays relying on an immunochemical complex formed by a reaction between a first constituent of said immunochemical complex and a second constituent of said immunochemical complex, which second constituent includes a fluorescent tag, said apparatus comprising in combination:

a radiation source capable of producing radiation having a first spectral energy distribution that can excite fluorescence in said fluorescent tag;

an optical fiber transmissive to radiation having said first spectral energy distribution and further being transmissive to radiation having a second spectral energy distribution corresponding to the fluorescence of said fluorescent tag;

means for injecting radiation of said first spectral energy distribution from said source into one end of said optical fiber;

means on said optical fiber for so attaching a plurality of said first constituents to the side surface of said fiber as to leave substantially unaffected the reactivity of said first constituent to form said immunochemical complex; and

means for detecting radiation of said second spectral energy distribution propagating within said fiber.

3. Apparatus as claimed in claim 2 wherein said means for attaching comprises a coating reactive with said plurality of first constituents.

4. Apparatus as claimed in claim 2 including a plurality of said first constituents attached to at least a portion of said side surface of said optical fiber by said means for attaching.

5. Apparatus as claimed in claim 4 wherein at least part of first constitutents are complexed with a predetermined amount of said constituents incorporating a fluorescent tag.

6. Apparatus as claimed in claim 4 wherein said first constitutents are antibodies.

7. Apparatus as claimed in claim 4 wherein said first constitutents are antigen-reactive antibody fragments.

8. Apparatus as claimed in claim 4 wherein said first constitutents are antigens.

9. Apparatus as claimed in claim 4 wherein said first constitutents are haptens.

10. Apparatus as defined in claim 2 wherein said means for detecting radiation is disposed for detecting said radiation of said first spectral energy exiting from said one end of said optical fiber.

11. In an immunoassay relying on a constituent of an immunochemical complex wherein said constituent includes a fluorescent tag, the improvement comprising:

immersing in a sample to be assayed an optical fiber transmissive to excitation radiation that can excite fluorescence of said tag and transmissive to fluorescent radiation from said tag, said optical fiber having selected constituents of said immunochemical complex attached to its surface for forming said immunochemical complex with said sample;

illuminating at least one end of said optical fiber with said excitation radiation so as to excite fluorescence of said fluorescent tag in said immunochemical complex attached to said optical fiber, said excitation radiation being supplied to said one end of said optical fiber over a solid angle equal to or smaller than that defined by the numerical aperture of said optical fiber so that said excitation radiation propagates within said optical fiber along paths substantially above the critical angle with regard to the side surface of said optical fiber;

collecting over a similar limited solid angle fluorescent radiation that arises from the excitation of said fluorescent tag in said immunochemical complex attached to said optical fiber and that exits from an end of said fiber; and

measuring the intensity of said fluorescent radiation exiting from said optical fiber.

12. The immunoassay as set forth in cliam 11 wherein said step of collecting is with respect to said fluorescent radiation exiting from said one end.