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Biospecific multianalyte assay method

Assignee: Wallac Oy
•
Filing: 1988-06-09
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Granted: 1991-07-02
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Expires: 2008-06-09
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Abstract

Abstract In a biospecific multianalyte assay the use of microspheres and fluorescent labels with substantially different fluorescence decay times, is combined. The assay is performed in a suspension of microspheres in the form of a pool of different microsphere categories, where the categories represent different analytes. The microspheres belonging to the respective categories are first coated with a specific reactant, i.e. the microspheres function as a solid support for the reactant and for a biospecific reaction. Fluorescent labels having a short decay time are used to identify the category of each individual microsphere, while fluorescent labels having a long decay time are used to determine the concentration of a particular analyte on the microsphere by means of the biospecific reaction.

Inventors

  • 👤 Erkki J. Soini

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 16:34
CPC Classifications
G; G01; G01N; G01N33/00; G01N33/48; G01N33/50; G01N33/53; G01N33/543; G01N33/54313; G01N21/00; G01N21/62; G01N21/63; G01N21/64; G01N21/6408; G01N33/58; G01N33/582; G01N15/00; G01N15/10; G01N15/14

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 193 words
Biospecific multianalyte assay method, characterized by preparing categories of microspheres representing different analytes to be assayed, said categories comprising different amounts of a fluorescent substance having a short decay time, coating each category of microspheres with a biospecific reactant, pooling the different categories of microspheres together in a suspension, adding a sample containing analytes to be assayed to the suspension, adding a mixture of biospecific reactants labelled with a fluorescent compound having a long decay time to the suspension to initiate biospecific reactions between the analytes and the belled reactants and microsphere-associated reactants, diluting the suspension to reduce the concentration of labelled reactants not bound to the microspheres, exciting both the fluorescent substance having a short decay time and the fluorescent compound having a long decay time, associated with the microspheres, to generate fluorescence emissions, converting the fluorescence emissions to electrical signals, identifying the category of each microsphere on the basis of the strength of the electrical signal resulting from the short decay time fluorescent substance, measuring the concentration of the analyte on each microsphere on the basis of the strength of the electrical signal resulting from the long decay time fluorescent compound.
Claim 2
Dependent Claim 193 words
Biospecific multianalyte assay method, characterized by preparing categories of microspheres representing different analytes to be assayed, said categories comprising different amounts of a fluorescent substance having a short decay time, coating each category of microspheres with a biospecific reactant, pooling the different categories of microspheres together in a suspension, adding a sample containing analytes to be assayed to the suspension, adding a mixture of biospecific reactants labelled with a fluorescent compound having a long decay time to the suspension to initiate biospecific reactions between the analytes and the belled reactants and microsphere-associated reactants, diluting the suspension to reduce the concentration of labelled reactants not bound to the microspheres, exciting both the fluorescent substance having a short decay time and the fluorescent compound having a long decay time, associated with the microspheres, to generate fluorescence emissions, converting the fluorescence emissions to electrical signals, identifying the category of each microsphere on the basis of the strength of the electrical signal resulting from the short decay time fluorescent substance, measuring the concentration of the analyte on each microsphere on the basis of the strength of the electrical signal resulting from the long decay time fluorescent compound.

References Cited (Backward Citations)

WO1980002076A1 Cited
GB2126341A Cited
EP0121262A2 Cited
EP0121442A2 Cited
US4584277A Cited
EP0126450A2 Cited
EP0193356A2 Cited
EP1219309A1 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1994-07-01 1994-12-31 1995-07-02 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1998-07-01 1998-12-31 1999-07-02 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2002-07-01 2002-12-31 2003-07-02 $7700.00 Window Closed / Lapsed

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