Enzymatic immunoassay involving detecting fluorescence while oscillating magnetic beads

• US 5,238,815 A
• Filed: 05/20/1992
• Issued: 08/24/1993
• Est. Priority Date: 08/30/1985
• Status: Expired due to Term

• Current Assignee: Toyo Soda Manufacturing Co., Ltd.
• Original Assignee: Toyo Soda Manufacturing Co., Ltd.
• Inventors: Kamada, Satoru, Higo, Yuji
• Primary Examiner(s): Rosen, Sam
• Application Number:
  US07/885,241
• Time in Patent Office: 461 Days
• Field of Search: 435/7.9, 435/7.92, 435/21
• US Class Current: 435/7.92
• CPC Class Codes: G01N 33/557 using kinetic measurement, i.e. time rate of progress of an antigen-antibody interaction
• CPC Class Codes: Y10S 435/808 Optical sensing apparatus
• CPC Class Codes: Y10S 436/80 Fluorescent dyes, e.g. rhodamine
• CPC Class Codes: Y10S 436/805 Optical property

Abstract

Enzymatic immunoassay for estimating the concentration of antigen or antibody comprising bringing an antigen-antibody complex, which is labelled by an enzyme and is present heterogeneously in a solution, into contact with a substrate where pH of the solution is so adjusted as to be suitable for the enzyme to be activated and also for measuring the fluorescence of the substrate, measuring the time-variation of fluorescent intensity of the substrate produced by the enzyme reaction, and estimating the concentration of the antigen or the antibody from the slope of the substantially linear portion, on a characteristic curve representing variation of the fluorescence intensity with the time.

Fluorescence is measured while magnetic beads with antigen-antibody complex attached are oscillated at a specific frequency.

Claims

1. In an enzymatic immunoassay for estimating the concentration of antigen or antibody in a sample, comprising bringing an antigen-antibody complex of said antigen and antibody, which is labelled by an enzyme into contact with a substrate which is converted into a substance emitting fluorescence by the enzyme, adjusting the pH of the solution to be suitable for the enzyme to be activated and for measuring the fluorescence of the substrate, measuring the variation as a function of time or fluorescent intensity of the substrate produced by the activation of the enzyme, the improvement comprising estimating the concentration of the antigen or the antibody from the slope of the substantially linear portion on a curve representing variation of the fluorescence intensity as a function of time, said complex being affixed to the surface of insoluble beads comprising magnetic material and the fluorescent intensity is measured while the beads are being oscillated at a frequency of 70 to 120/min, wherein said enzyme is alkaliphosphatase, said substrate is 4-methylumbeliferone, said immunoassay is free from the requirement of correcting the zero point and said immunoassay is free from the requirement of controlling the time.

2. The immunoassay of claim 1, wherein the error is less than 1%.