A new immunoassay based on fluorescence excitation by internal reflection spectroscopy

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Abstract

A new immunoassay technique is described which uses totally internally reflected light to excite the fluorescence of fluorescein labeled antibody which has become bound to a hapten-protein conjugate adsorbed on a quartz-plate in the antibody solution. The presence of any free hapten in solution reduces the amount of antibody free to bind to the surface and thus reduces the fluorescence signal. Measurement of the decrease of the fluorescent signal then gives a measure of the concentration of free hapten present. The technique is simple, fast and has high intrinsic sensitivity and specificitty. It has been demonstrated for phenyl arsonic acid and morphine. Free morphine at a concentration of 2 × 10−7 M is readily detected.

References (14)

  • C.K. Carniglia et al.

    J. Opt. Soc. Amer.

    (1972)
  • P. Cuatrecasas et al.

    Ann. Rev. Biochem.

    (1971)
  • M. Goldman

    Fluorescent Antibody Techniques

  • M. Goldman

    Fluorescent Antibody Techniques

  • N.J. Harrick

    Internal Reflection Spectroscopy

    (1967)
  • N.J. Harrick

    Internal Reflection Spectroscopy

  • N.J. Harrick et al.

    Anal. Chem.

    (1973)
There are more references available in the full text version of this article.

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Present address: Laboratory of Chemical Biodynamics, Lawrence Berkeley Laboratory, University of California, Berkeley, Ca. 94720, U.S.A.

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