Absorbance modulated fluorescence detection methods and sensors

• US 5,143,853 A
• Filed: 02/02/1989
• Issued: 09/01/1992
• Est. Priority Date: 06/25/1986
• Status: Expired due to Term

• Current Assignee: Trustees of Tufts College
• Original Assignee: Trustees of Tufts College
• Inventors: Walt, David R.
• Primary Examiner(s): Kepplinger, Esther L.
• Assistant Examiner(s): Scheiner, Toni R.
• Application Number:
  US07/305,176
• Time in Patent Office: 1,307 Days
• Field of Search: 435/808, 436/507, 436/518, 436/528, 436/536, 436/546, 436/172, 436/800, 436/805, 436/56, 436/164, 436/165, 422/55, 422/59, 422/901, 358/901, 350/96.1, 350/96.2, 350/96.3, 350/96.17
• US Class Current: 436/501
• CPC Class Codes: G01N 2021/6434 Optrodes
• CPC Class Codes: G01N 2021/7793 Sensor comprising plural indicators
• 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 21/7703 using reagent-clad optical fibres or optical waveguides using measurement of total internal reflection or attenuated total reflection G01N21/552; optical fibres or waveguides per se G02B
• CPC Class Codes: G01N 2201/06193 Secundary in-situ sources, e.g. fluorescent particles
• CPC Class Codes: G01N 33/582 with fluorescent label
• 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
• CPC Class Codes: Y10T 436/13 Tracers or tags

Abstract

A variety of methods and apparatus for the detection of an analyte of interest in a fluid sample is provided which relies upon the interaction of a fluorophore and a chromophoric light absorbing compound for qualitative and quantitative results. The methods preferably employ fiber optic sensors in combination with fluorophores and/or proto-absorber substances in mobile and immobilized modes of use. The methods and apparatus rely upon the ability of the light absorbing compositions to absorb energy which is transferred either radiatively or non-radiatively by the fluorophore when in an excited state.

Claims

1. A method for detecting an analyte of interest in a fluid sample, said method comprising the steps of:

admixing the fluid sample comprising a discrete absorber ligand whose spectral properties are influenced by and correlatable with the analyte of interest in the sample with a chemically non-reactive fluorophore to form a reaction mixture, said absorber ligand having a definable light absorption spectrum, said fluorophore having a definable light absorption spectrum and a definable light emission spectrum each of which overlaps the light absorption spectrum of said absorber ligand, said fluorophore of said formed reaction mixture being able

(a) to absorb exciting light energy of a first wavelength,

(b) to transfer a part of said fluorophore absorbed energy to said absorber ligand of said reaction mixture for absorption, said transfer being selected from the group consisting of radiative and non-radiative energy transfers, and

(c) to emit the other part of said fluorophore absorbed energy as emitted light of a second wavelength;

introducing exciting light energy of the first wavelength to said reaction mixture sufficient to cause said fluorophore to absorb said exciting light energy, wherein a portion of said fluorphore absorbed energy is transferred to and absorbed by such absorber ligand as is present in said reaction mixture, and wherein another portion of said fluorophore absorbed energy is emitted by said fluorophore as light of the second wavelength; and

detecting said light of the second wavelength emitted by said fluorophore of said reaction mixture, said detected emitted light being a measure of the analyte of interest in the sample.

7. The method as recited in claim 1, 2, 3, 4, 5, or 6 wherein said fluorophore is immobilized using a porous matrix.

9. The method as recited in claim 1, 2, 3, 4, 5, or 6 wherein said discrete ligand is a fluorescent material.

10. The method as recited in claim 1, 2, 3, 4, 5, or 6 wherein the analyte of interest and said discrete ligand are identical.

11. The method as recited in claim 1, 2, 3, 4, 5, or 6 wherein said introduction of exciting light is achieved using a fiber optic sensor.

12. The method as recited in claim 1, 2, 3, 4, 5, or 6 wherein said detection of emitted light from said admixture is achieved using a fiber optic sensor.

13. The method as recited in claim 1, 2, 3, 4, 5, or 6 wherein said fluorophore is selected from the group consisting of eosin, eosin derivatives, rhodamine, rhodamine derivatives, fluorescein, fluorescein derivatives, acridine, acridine derivatives, erhthroscein, and cyanosine.

2. A method for detecting an analyte of interest in a fluid sample, said method comprising the steps of:

mixing the fluid sample comprising a discrete ligand whose presence is indicative of the analyte of interest in the sample with a specifically binding protoabsorber whose spectral properties are influenced by and correlatable with said ligand to form an absorption complex having a definable light absorption spectrum, at least a portion of said proto-absorber binding with such ligand as is present to form said absorption complex while the remainder of said proto-absorber remains unbound;

admixing a chemically non-reactive fluorophore with said absorption complex to form a reaction mixture, said fluorophore having a definable light absorption spectrum and a definable light emission spectrum each of which overlaps the light absorption spectrum of said absorption complex, said fluorophore of said formed ereaction mixture being able

(a) to absorb exciting light energy of a first wavelength,

(b) to transfer a part of said fluorophore absorbed energy to said absorber complex of said reaction mixture for absorption, said transfer being selected from the group consisting of radiative and non-radiative energy transfers, and

(c) to emit the other part of said fluorophore absorbed energy as emitted light of a second wavelength;

introducing exciting light energy of the first wavelength to said reaction mixture sufficient to cause said fluorophore to absorb said exciting light energy, wherein a portion of said fluorphore absorbed energy is transferred to and absorbed by such absorber complex as is present in said reaction mixture, and wherein another portion of said fluorophore absorbed energy is emitted by said fluorophore as light of the second wavelength; and

detecting said light of the second wavelength emitted by said fluorophore of said reaction mixture, said detected emitted light being a measure of the analyte of interest in the sample.

8. The method as recited in claim 2, 3, 4, 5, or 6 wherein said proto-absorber is immobilized using a porous matrix.

14. The method as recited in claim 2, 3, 5, or 6 wherein said proto-absorber is selected from the group consisting of phenol red, brilliant yellow, rosolic acid, pararosaniline, ortho cresolphthalein, and bromo pyrogalol red.

3. A method for detecting an analyte of interest in a fluid sample, said method comprising the steps of:

mixing the fluid sample comprising a discrete ligand whose presence is indicative of the analyte of interest in the sample with a specifically binding proto-absorber whose spectral properties are influenced by and correlatable with said ligand and which has a definable light absorption spectrum in the unbound state, at least a portion of said proto-absorber binding with such ligand as is present to form a complex while the remainder of said proto-absorber remains unbound;

admixing a chemically non-reactive fluorophore with said unbound proto-absorber to form a reaction mixture, said fluorophore having a definable light absorption spectrum and a definable light emission spectrum each of which overlaps the light absorption spectrum of said unbound proto-absorber, said fluorophore of said formed reaction mixture being able

(a) to absorb exciting light energy of a first wavelength,

(b) to transfer a part of said fluorophore absorbed energy to said unbound proto-absorber of said reaction mixture for absorption, said transfer being selected from the group consisting of radiative and non-radiative energy transfers, and

(c) to emit the other part of said fluorophore absorbed energy as emitted light of a second wavelength;

introducing exciting light energy of the first wavelength to said reaction mixture sufficient to cause said fluorophore to absorb said exciting light energy, wherein a portion of said fluorophore absorbed energy is transferred to and absorbed by such unbound proto-absorber as is present in said reaction mixture, and wherein another portion of said fluorophore absorbed energy is emitted by said fluorophore as light of the second wavelength; and

detecting said light of the second wavelength emitted by said fluorophore of said reaction mixture, said detected emitted light being a measure of the analyte of interst in the sample.

4. A method for detecting an analyte of interest in a fluid sample, said method comprising the steps of:

admixing the fluid sample comprising a discrete absorber ligand whose spectral properties are influenced by and correlatable with the analyte of interest in the sample with a plurality of different chemically non-reactive fluorophores to form a reaction mixture, said absorber ligand having a definable light absorption spectrum, each of said different fluorophores having a definable light absorption spectrum and a definable light emission spectrum wherein at least one of said different fluorophores has a definable light absorption spectrum which overlaps the light absorption spectrum of said absorber ligand and another of said different fluorophores has a definable light emission spectrum which overlaps the light absorption spectrum of said absorber ligand, and wherein

(a) at least one fluorophore of said formed reaction mixture is able to absorb exciting light energy of a first wavelength and to transfer at least a part of said fluorophore absorbed energy to another fluoropbore for energy absorption,

(b) at least one other fluorophore of said reaction mixture is able to absorb energy transferred from a different fluorophore and to emit at least part of said absorbed energy as emitted light of a second wavelength, and

(c) at least one of said different fluorophores transfers at least a part of said fluorophore absorbed energy to said absorber ligand for absorption, said transfer being selected from the group consisting of radiative and non-radiative energy transfers;

introducing exciting light energy of the first wavelength to said reaction mixture sufficient to cause at least one of said different fluorophores to absorb said exciting light energy wherein portions of said fluorophore absorbed energy are transferred to and absorbed by at least one other of said fluorophores and such absorber ligand as is present in said reaction mixture, and wherein at least one other portion of said fluorophore absorbed energy is emitted by said fluorophore as light of the second wavelength; and

detecting said light of the second wavelength emitted by said fluorophore of said reaction mixture, said detected emitted light being a measure of the analyte of interest in the sample.

5. A method for detecting an analyte of interest in a fluid sample, said method comprising the steps of:

mixing the fluid sample comprising a discrete ligand whose presence is indicative of the analyte of interest in the sample with a specifically binding proto-absorber whose spectral properties are influenced by and correlatable with said ligand to form an absorption complex having a definable light absorption spectrum, at least a portion of said proto-absorber binding with such ligand as is present to form said absorption complex while the remainder of said proto-absorber remains unbound;

admixing a plurality of different chemically non-reactive fluorophores with said absorption complex to form a reaction mixture, each of said fluorophores having a definable light absorption spectrum and a definable light emission spectrum wherein at least one of said different fluorophores has a definable light absorption spectrum which overlaps the light absorption spectrum of said absorption complex and another of said different fluorophores has a definable light emission spectrum which overlaps the light absorption spectrum of said absorption complex, and wherein

(a) at least one fluorophore of said formed reaction mixture is able to absorb exciting light energy of a first wavelength and to transfer a part of said fluorophore absorbed energy to another fluorophore for energy absorption,

(b) at least one other fluorophore is able to absorb energy transferred from a different fluorophore and to emit said absorbed energy as emitted light of a second wavelength,

(c) at least one of said fluorophores transfers at least a part of said fluorophore absorbed energy to said absorption complex for energy absorption, said transfer being selected from the group consisting of radiative and non-radiative energy transfers;

introducing exciting light energy of the first wavelength to said reaction mixture sufficient to cause at least one of said different fluorophores to absorb said exciting light energy, wherein portions of said fluorophore absorbed energy are transferred to and absorbed by at least one other of said fluorophores and such absorber complex as is present in said reaction mixture, and wherein a portion of said fluorophore absorbed energy is emitted by a fluorophore as light of the second wavelength; and

detecting said light of the second wavelength emitted by said fluorophore of said reaction mixture, said detected emitted light being a measure of the analyte of interest in the sample.

6. A method for detecting an analyte of interest in a fluid sample, said method comprising the steps of:

mixing the fluid sample comprising a discrete ligand whose presence is indicative of the analyte of interest in the sample with a specifically binding proto-absorber whose spectral properties are influenced by and correlatable with said ligand and which has a definable light absorption spectrum in the unbound state, at least a portion of said proto-absorber binding with such ligand as is present to form a complex while the remainder of said proto-absorber remains unbound;

admixing a plurality of different chemically non-reactive fluorophores with said unbound proto-absorber to form a reaction mixture, each of said fluorophores having a definable light absorption spectrum and a definable light emission spectrum wherein at least one of said different fluorophores has a definable light absorption spectrum which overlaps the light absorption spectrum of said unbound proto-absorber and another of said different fluorophores has a definable light emission spectrum which overlaps the light absorption spectrum of said unbound proto-absorber, and wherein

(a) at least one fluorophore of said formed reaction mixture is able to absorb exciting light energy of a first wavelength and to transfer a part of said fluorophore absorbed energy to another fluorophore for energy absorption,

(b) at least one other fluorophore is able to absorb energy transferred from a different fluorophore and to emit said absorbed energy as light of a second wavelength,

(c) at least one of said fluorophores transfers at least a part of said fluorophore absorbed energy to said unbound proto-absorber for energy absorption, said transfer being selected from the group consisting of radiative and non-radiative energy transfers;

introducing exciting light energy of the first wavelength to said reaction mixture sufficient to cause at least one of said different fluorophore to absorb said exciting light energy, wherein portions of said fluorophore absorbed energy are transferred to and absorbed by at least one other of said fluorophores and such unbound proto-absorber as is present in said reaction mixture, and wherein a portion of said fluorophore absorbed energy is emitted by a fluorophore as light of the second wavelength; and

detecting said light of the second wavlength emitted by said fluorophore of said reaction mixture, said detected emitted light being a measure of the analyte of interest in the sample.