Fluorescent immunoassay employing optical fiber in capillary tube

• US 4,447,546 A
• Filed: 08/23/1982
• Issued: 05/08/1984
• Est. Priority Date: 08/23/1982
• Status: Expired due to Term

• Current Assignee: Roche Diagnostics Corporation (Roche Holding AG)
• Original Assignee: Myron J. Block
• Inventors: Hirschfeld, Tomas E.
• Primary Examiner(s): Marantz, Sidney
• Application Number:
  US06/410,340
• Time in Patent Office: 624 Days
• Field of Search: 436/527, 436/805, 436/807, 422/56, 422/57, 250/227, 250/365, 356/445
• US Class Current: 436/527
• CPC Class Codes: G01N 2021/0346 Capillary cells; Microcells
• 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: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• 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

Fluorescent immunoassay apparatus and method employing a disposable consisting, in a preferred embodiment, of a short length of precise diameter capillary tubing having an axially disposed optical fiber to which is immobilized a monolayer of a component of the antibody-antigen complex (e.g., an antibody), an inert diluent, and a preload of a known amount of tagged complement to the immobilized component (e.g., a fluorescent-tagged antigen). The dimensions of the fiber and the capillary tubing are chosen so as to allow the tube to fill itself by capillary action once an end of the tube is immersed into the sample. Precise timing and ballistic measurements may, if desired, be avoided by insuring the incubation time is larger than the diffusion time necessary to scavenge the volume between the fiber and the capillary tubing. Fluorimetric measurement is made by total reflection fluorescence techniques.

Claims

1. Apparatus for performing immunoassays using an antigen-antibody complex incorporating a fluorescent tag capable of emitting fluorescent radiation when excited by exciting radiation, said apparatus comprising in combination:

an optical fiber transmissive to both said exciting radiation and said fluorescent radiation;

a coating on at least a portion of said fiber, said coating having a plurality of sites, each being capable of having attached thereto a selected moiety of said antigen-antibody complex so as to leave substantially unaffected the activity of said selected moiety for forming said antigen-antibody complex; and

means for controlling a volume of capillary dimensions bounded by said portion of said fiber.

2. Apparatus according to claim 1 wherein said coating is on a predetermined length of said fiber.

3. Apparatus according to claim 1 wherein a plurality of selected moieties of said antigen-antibody complex are attached to said coating.

4. Apparatus according to claim 3 wherein said selected moieties are attached to substantially all of said plurality of sites.

5. Apparatus according to claim 3 wherein said selected moieties and a plurality of particles of an immunologically inert material are attached in a predetermined ratio to substantially all of said plurality of sites.

6. Apparatus according to claim 5 wherein a plurality of tagged complement to said moieties are complexed to said moieties.

7. Apparatus according to claim 1 wherein said capillary dimensions are predetermined.

8. Apparatus according to claim 7 wherein said means for controlling comprises an elongate enclosure means dimensioned to surround said fiber in a spaced-apart relationship of capillary dimensions and means for positioning said fiber in said relationship within said enclosure means.

9. Apparatus according to claim 8 wherein said elongate enclosure means is a capillary tube.

10. Apparatus according to claim 9 wherein at least a portion of the interior of said capillary tube is provided a reagent coating.

11. Apparatus according to claim 9 wherein said means for positioning said fiber includes a substantially centrally apertured stopper mounted in a first end of said capillary tube, said fiber being positioned in said aperture.

12. Apparatus according to claim 11 wherein said stopper is provided with locating means for defining the location of an end of said fiber.

13. Apparatus according to claim 11 wherein the opposite end of said capillary tube is dimensioned to have a smaller inside diameter than the remainder of said capillary tube.

14. Apparatus for performing immunoassays wherein a fluorescent tag capable of emitting fluorescent radiation when excited by more energetic exciting radiation is incorporated in a constituent of an antigen-antibody complex, said apparatus comprising in combination:

an optical fiber transmissive to both said exciting radiation and said fluorescent radiation, a predetermined length of said fiber having immobilized thereto a selected moiety of a desired antigen-antibody complex in a predetermined surface concentration;

a capillary tube dimensioned to accept said fiber in spaced-apart relationship; and

a stopper affixed to a first end of said capillary tube, said stopper supporting said fiber substantially coaxially within said capillary tube with said fiber passing through said stopper substantially centrally, said stopper having a locating means for defining the location of an end of said fiber.

15. A method for immunoassay employing an optical element transmissive to excitation radiation which can excite fluorescence of a fluorescent tag included as a constituent of an antigen-antibody complex, said element being also transmissive to said fluorescence, said optical element having selected moieties of said antibody-antigen complex attached to a pre-determined area of its surface, said method comprising the steps of:

immersing said optical element in a fluid sample to be assayed so that the portion of said sample immunologically reactive with said selected moieties can react therewith to form said complex;

controlling the immersion of said optical element in said fluid sample so as to insure that said predetermined area is completely covered with a layer of known thickness of said fluid sample;

incubating said optical element in said layer of fluid sample for a time in excess of the time required for diffusional processes to scavenge the volume of sample defined by said known area and said known thickness;

illuminating said optical element with an evanescent electromagnetic wave of said excitation radiation so as to excite fluorescence of said tag in said complex attached to said optical element; and

measuring the intensity of said fluorescence.