Double tagged immunoassay

• US 4,385,126 A
• Filed: 11/19/1980
• Issued: 05/24/1983
• Est. Priority Date: 11/19/1980
• Status: Expired due to Term

• Current Assignee: BioWhittaker, Inc. (Lonza Group AG)
• Original Assignee: International Diagnostic Technologies Incorporated
• Inventors: Maggio, Edward T., Chen, Janet H., Rehbinder, Dietrich
• Primary Examiner(s): Fagelson, Anna P.
• Application Number:
  US06/217,011
• Time in Patent Office: 916 Days
• Field of Search: 424/8, 424/12, 23/230 B, 436/500, 436/508, 436/518, 436/546, 436/800
• US Class Current: 436/518
• CPC Class Codes: G01N 33/54306 Solid-phase reaction mechanisms
• CPC Class Codes: G01N 33/582 with fluorescent label
• CPC Class Codes: Y10S 436/80 Fluorescent dyes, e.g. rhodamine

Abstract

Immunoassays are performed with two different ligands tagged with two different tagging constituents which are independent of each other and the two tagged ligands are immunologically bound together. The two different ligands may be detected independently through their independent tagging constituents for quality control, internal calibration (standardization), determination of viability and shelf life and the like.

Claims

1. In a method of performing an immunoassay in which a receptor ligand is contacted with a test ligand which binds immunologically with the receptor ligand and the receptor and/or test ligands are contacted with an assay ligand which is capable of immunologically binding to the receptor and/or test ligand the improvement which comprises employing a receptor ligand containing a tagging constituent which is independent of the tagging constituent on the test ligand.

2. The method of claim 1 which further includes the steps of quantitatively detecting at least one of the tagged constituents after contacting the receptor ligand and the test ligand.

3. In a method of performing an immunoassay in which a receptor ligand is contacted with a test ligand which binds immunologically with the receptor ligand and the receptor and/or test ligands are contacted with an assay ligand which is capable of immunologically binding to the receptor and/or test ligand the improvement which comprises employing a receptor ligand containing a tagging constituent which is independent of the tagging constituent on the test ligand, and measuring the quantity of assay ligand by measuring the quantities of tagging constituents on both the receptor ligand and test ligand while said receptor and test ligand are immunologically bound together.

4. The method of claim 3 in which said measurement is performed by detecting fluorescent light from both the receptor and test ligands with the same fluorometer.

5. The method of claim 3 in which the receptor and/or test ligand is supported on a surface.

6. The method of claim 3 in which the two tagging constituents are formed of fluorescent materials which fluoresce at different wavelengths.