Optical method for measuring an analyte using area-modulated luminescence

• US 5,190,857 A
• Filed: 06/05/1991
• Issued: 03/02/1993
• Est. Priority Date: 05/19/1989
• Status: Expired due to Term

• Current Assignee: Acrogen, Inc.
• Original Assignee: Acrogen, Inc.
• Inventors: Bustamante, Carlos, Dorman, Burton P., Niemczyk, Thomas M., Allen, Fritz S.
• Primary Examiner(s): Hill, Jr., Robert J.
• Application Number:
  US07/710,669
• Time in Patent Office: 636 Days
• Field of Search: 436/172, 436/537, 436/546, 436/800, 436/805, 422/82.08, 422/82.07, 435/7.1, 435/7.21, 435/968, 356/317, 356/318, 356/417, 250/365, 250/458.1, 250/459.1, 250/461.1, 250/461.2
• US Class Current: 435/7.21
• CPC Class Codes: G01N 2021/178 Methods for obtaining spatial resolution of the property being measured
• CPC Class Codes: G01N 2021/6469 Cavity, e.g. ellipsoid
• 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 33/582 with fluorescent label
• CPC Class Codes: Y10S 435/968 High energy substrates, e.g. fluorescent, chemiluminescent, radioactive
• CPC Class Codes: Y10S 436/80 Fluorescent dyes, e.g. rhodamine
• CPC Class Codes: Y10S 436/805 Optical property

Abstract

A luminescence measuring system is provided for detecting luminescence at extremely low concentrations of luminescing moieties. The method employs alternating radiation at a plurality of loci of an inhomogenous solution, where the radiant power is maintained constant, and the irradiated volumes of pairs of loci are systematically varied. With the probability being very low that the same luminescence signal will be obtained in the two or more measurements, by comparing the measurements, one can detect a low luminescence signal in the presence of relatively high noise levels. Various techniques are described for modulating the irradiance and detecting changes in signal.

Claims

1. A method for determining the presence of an analyte in a sample employing a luminescence label, wherein at least two different regions of different volumes of an assay medium are irradiated and the number of luminescent moieties related to the amount of analyte are inhomogeneously distributed in said regions, said method comprising:

irradiating sequentially said at least two different volumes of said assay medium comprising luminescent moieties present in an amount related to the amount of analyte in said sample, said irradiating being, for a given wavelength distribution, at a constant radiant power or at a constant photon flux at each of said volumes and under the same conditions except for said difference in volume;

detecting the light emitted from said volumes and determining the difference in light emission from each of said volumes,

wherein said difference is related to the presence of analyte in said sample.

2. A method according to claim 1, wherein said irradiating of said different volumes and said detecting is cycled to obtain a plurality of values for each of said volumes;

and including the additional step of determining the difference in light emission from each of said volumes and averaging said difference or of averaging the light emission from each of said volumes and determining the difference of said averages.

3. A method according to claim 1, wherein said luminescent moieties are fluorescent particles, or cells or portions of cells.

4. A method according to claim 1, wherein said volumes comprise an overlapping region.

5. A method according to claim 1, wherein said volumes share a common center.

6. A method according to claim 1, wherein at least four volumes are irradiated, with pairs of volumes having overlapping regions.

7. A method according to claim 1, wherein said volumes comprise non-overlapping regions.

8. A method according to claim 1, wherein said volumes are of a constant thickness.

9. A method for determining the presence of an analyte in a sample employing a luminescence label, wherein at least two different regions of different volumes of an assay medium are irradiated and the number of luminescent moieties related to the amount of analyte are inhomogeneously distributed in said regions, said method comprising:

combining in an assay medium said sample with a fluorescent labeled conjugate capable of binding to a plurality of sites on said analyte to form luminescent moieties;

irradiating sequentially said at least two different volumes of said assay medium comprising luminescent moieties present in an amount related to the amount of analyte in said sample, said irradiating being, for a given wavelength distribution, at a constant radiant power or at a constant photon flux at each of said volumes and under the same conditions except for said difference in volume, wherein a portion of said volumes overlap;

detecting the light emitted from said volumes and determining the difference in light emission from each of said volumes,

wherein said difference is related to the presence of analyte in said sample.

10. A method according to claim 9, wherein said irradiating of said different volumes and said detecting is cycled to obtain a plurality of values for each of said volumes;

and including the additional step of determining the difference in light emission from each of said volumes and averaging said difference or of averaging the light emission from each of said volumes and determining the difference of said averages.

11. A method according to claim 10, wherein the luminescence signal fluctuations for each of said volumes and the magnitude of said volumes are used to determine the concentration of analyte in said sample.

12. A method for determining the presence of an analyte in a sample employing a luminescence label, wherein at least two different regions of different volumes of an assay medium are irradiated and the number of luminescent moieties related to the amount of analyte are inhomogeneously distributed in said regions, said method comprising:

combining in an assay medium fluorescent particles capable of aggregating in the presence or absence of analyte with said sample so as to cause or inhibit the formation of aggregations as luminescent moieties in relation to the amount of analyte present in said sample;

irradiating sequentially said at least two different volumes of said assay medium comprising luminescent moieties present in an amount related to the amount of analyte in said sample, said irradiating being, for a given wavelength distribution, at a constant radiant power or at a constant photon flux at each of said volumes and under the same conditions except for said difference in volume;

detecting the light emitted from said volumes and determining the difference in light emission from each of said volumes,

wherein said difference is related to the presence of analyte in said sample.

13. A method according to claim 12, wherein said irradiating of said different volumes and said detecting is cycled to obtain a plurality of values for each of said volumes;

and including the additional step of determining the difference in light emission from each of said volumes and averaging said difference or of averaging the light emission from each of said volumes and determining the difference of said averages.