Method and apparatus for the measurement of analyte concentration levels by the steady-state determination of fluorescence lifetime

• US 5,626,134 A
• Filed: 04/20/1995
• Issued: 05/06/1997
• Est. Priority Date: 04/21/1994
• Status: Expired due to Term

• Current Assignee: Cellview Imaging Inc.
• Original Assignee: Ralph Zuckerman
• Inventors: Zuckerman, Ralph
• Primary Examiner(s): Sykes, Angela D.
• Assistant Examiner(s): WINAKUR, ERIC FRANK
• Application Number:
  US08/425,757
• Time in Patent Office: 747 Days
• Field of Search: 128/633, 128/634, 128/665, 356/41, 250/461.1
• US Class Current: 600/317
• CPC Class Codes: A61B 5/14555 specially adapted for the eye fundus
• CPC Class Codes: G01N 21/6445 Measuring fluorescence polarisation

Abstract

The use of luminescent probe substances is detailed in methods and an apparatus for the determination of the concentration and distribution in space and time of numerous analytes of biologic and physical import in vivo and in vitro by the steady-state determination of luminescence lifetime. In the instance of analytes that quench excited states, a fluorophore whose excited state is quenched by the analyte in question is free to undergo Brownian rotation alone or when conjugated to a carrier molecule within a medium of suitable viscosity. The analysis medium is irradiated with continuous linearly polarized light at a wavelength strongly absorbed by the fluorophore. The emitted luminescence is resolved into its vector components parallel and perpendicular to the plane of polarization of the excitation light, thereby permitting the calculation of the luminescence anisotropy of the irradiated specimen. The concentration of the quencher is determined by applying a mathematical function which relates the luminescence anisotropy of the fluorophore to the concentration of the quencher. For the determination of the concentration of substances which do not themselves quench excited states a known quantity of the analyte is conjugated to a quencher molecule or an energy transfer acceptor molecule and a competition reaction is set up in which the luminescently labelled substance and the unlabelled substance within the sample compete for sites on a labelled carrier molecule. To the extent that the concentration of unlabelled substance in the sample increases and displaces labelled material on the carrier molecule the luminescence lifetime of the carrier fluorophore will increase. The luminescence anisotropy is measured at the emission band of the luminescent label on the carrier molecule and the concentration of the substance under measurement is determined by applying an empirically determined mathematical function which relates luminescence anisotropy to the concentration of the analyte.

Claims

1. A method of measuring concentration of an analyte in a medium, the method comprising the steps of:

a) introducing, into the medium, a probe substance which becomes luminescent when irradiated and whose luminescence is quenched by the analyte in the medium,

b) irradiating the medium with linearly polarized light so as to cause the probe substance to become luminescent,

c) resolving luminescence emitted by the probe substance into vector components parallel and perpendicular to a plane of polarization of said linearly polarized light,

d) calculating a luminescence anisotropy, as a function of said vector components, in space or in time, of the irradiated medium, and

e) applying a mathematical function which relates said luminescence anisotropy to said concentration of the analyte in said medium, the mathematical function being in the form of an equation.

2. The method of claim 1, further comprising the step of calculating a luminescence lifetime of the probe substance according to the following equation:

##EQU7## wherein τ

is the luminescence lifetime, is the concentration of the analyte, K_D is a dynamic quench constant, and τ

₀ is a luminescence lifetime in the absence of analyte.

3. The method of claim 1, further comprising the step of selecting the equation as follows:

##EQU8## wherein A is fluorescence anisotropy, defined as ##EQU9## wherein I.sub.

and I.sub.⊥

are intensities of luminescence emission with their electric vectors respectively parallel and perpendicular to the linearly polarized light of step (b), G is an empirical correction factor used to correct for transmission efficiency in parallel and perpendicular planes, R is mean molecular rotation time in radians/sec, A_o is fluorescence anisotropy in a "frozen" state, in the absence of Brownian rotation, K_D is a dynamic quench constant, τ

_o is luminescence lifetime in the absence of quencher, and is the concentration of the analyte which is to be determined.

4. The method of claim 1, further comprising the step of determining a topographic distribution of said analyte concentration in said medium.

5. The method of claim 1, wherein the probe substance is disposed in an optical sensor which comprises a tip and a thermistor, the method further comprising the step of correcting anisotropy measurements for temperature of the tip of the sensor according to the following equation:

##EQU10## wherein R_g is a gas constant, T is temperature, η

is viscosity, V is hydrodynamic volume of the probe substance, A is luminescence anisotropy, A_o is a luminescence anisotropy in a "frozen " state, in the absence of Brownian rotation, and τ

is a fluorescence lifetime.

6. The method of claim 1, further comprising the step of determining tomographically a topographic distribution of said analyte concentration within the medium by means of optical serial sectioning methodologies.

7. A method of measuring concentration of an analyte in a medium, the method comprising the steps of:

a) conjugating probe molecules to a carrier which has an affinity for the analyte, and adding the carrier to the medium, wherein the probe molecules are chosen such that they become luminescent when irradiated,

b) adding to the medium a quantity of the analyte conjugated with a substance selected from the group consisting of a quencher of luminescence energy of the probe molecules and an energy transfer acceptor of luminescence energy of the probe molecules,

c) irradiating the medium with linearly polarized light so as to cause the probe molecules to become luminescent,

d) resolving luminescence emitted by the probe molecules into vector components parallel and perpendicular to a plane of polarization of said linearly polarized light,

e) calculating a luminescence anisotropy, as a function of said vector components, in space or in time, of the irradiated medium, and

f) applying an empirically determined mathematical function which relates said luminescence anisotropy to said concentration of analyte in said medium.

8. The method of claim 7, wherein the luminescence anisotropy (A) of step (e) is defined as:

##EQU11## wherein I.sub.

and I.sub.⊥

, are intensities of luminescence emission with their electric vectors respectively parallel and perpendicular to the linearly polarized light of step (c), and G is an empirical correction factor used to correct transmission efficiency in parallel and perpendicular planes.

9. The method of claim 7, further comprising the step of determining a topographic distribution of said analyte concentration in said medium.

10. The method of claim 7, wherein the probe molecules are disposed in an optical sensor which comprises a tip and a thermistor, the method further comprising the step of correcting anisotropy measurements for temperature of the tip of the sensor by means of an empirically determined mathematical function.

11. The method of claim 7, further comprising the step of determining tomographically a topographic distribution of said analyte concentration within the medium by means of optical serial sectioning methodologies.

12. A method of measuring concentration of an analyte in a medium, the method comprising the steps of:

a) conjugating probe molecules to a carrier which has an affinity for the analyte, and adding the carrier to the medium, wherein the probe molecules are chosen such that they become luminescent when irradiated,

b) adding to the medium a known quantity of the analyte conjugated with a substance selected from the group consisting of a quencher of luminescence energy of the probe molecules and an energy transfer acceptor of luminescence energy of the probe molecules,

c) adding to the medium a sample to be analyzed which contains an unknown quantity of the analyte,

d) irradiating the medium with linearly polarized light so as to cause the probe molecules to become luminescent,

e) resolving luminescence emitted by the probe molecules into vector components parallel and perpendicular to a plane of polarization of said linearly polarized light,

f) calculating a luminescence anisotropy, as a function of said vector components, in space or in time, of the irradiated medium, and

g) applying an empirically determined mathematical function which relates said luminescence anisotropy to said concentration of the unknown quantity of analyte in said medium.

13. The method of claim 12, wherein the luminescence anisotropy (A) of step (f) is defined as:

##EQU12## wherein I.sub.

and I.sub.⊥

are intensities of luminescence emission with their electric vectors respectively parallel and perpendicular to the linearly polarized light of step (d), and G is an empirical correction factor used to correct transmission efficiency in parallel and perpendicular planes.

14. The method of claim 12, further comprising the step of determining a topographic distribution of said analyte concentration in said medium.

15. The method of claim 12, wherein the probe molecules are disposed in an optical sensor which comprises a tip and a thermistor, the method further comprising the step of correcting anisotropy measurements for temperature of the tip of the sensor by means of an empirically determined mathematical function.

16. The method of claim 12, further comprising the step of determining tomographically a topographic distribution of said analyte concentration within the medium by means of optical serial sectioning methodologies.

17. Apparatus for measuring a concentration of an analyte, comprising:

a) means for directing polarized light to an optical sensor,

b) the optical sensor comprising means for housing a probe substance which becomes luminescent when irradiated with light, the probe substance being chosen such that its luminescence is quenched by the analyte,

c) means for resolving said luminescence, emitted by the probe substance, into vector components parallel and perpendicular to a plane of polarization of said polarized light, and for detecting intensities of said vector components, and

d) means for processing the intensities obtained from the resolving and detecting means, the processing means comprising means for calculating said concentration of the analyte based on values of said intensities.

18. The apparatus of claim 17, wherein the optical sensor contains a viscous medium, the probe substance and the viscous medium being separated from the analyte by a membrane permeable to the analyte.

19. The apparatus of claim 17, wherein the calculating means comprises means for calculating analyte concentration according to the following equation:

##EQU13## wherein A is fluorescence anisotropy, defined as ##EQU14## wherein I.sub.

and I.sub.⊥

are intensities of luminescence emission with their electric vectors respectively parallel and perpendicular to the polarized light originating from the directing means, G is an empirical correction factor used to correct for transmission efficiency in parallel and perpendicular planes, R is mean molecular rotation time in radians/sec, A_o is fluorescence anisotropy in a "frozen" state, in the absence of Brownian rotation, K_D is a dynamic quench constant, τ

is a luminescence lifetime in the absence of quencher, and is the concentration of the analyte which is to be determined.

20. The apparatus of claim 17, wherein the analyte is disposed in a medium, the apparatus further comprising means for determining a topographic distribution of said analyte concentration in said medium.

21. The apparatus of claim 17, wherein the optical sensor comprises a tip and a thermistor, the apparatus further comprising means for correcting anisotropy measurements for temperature of the tip of the sensor according to the following equation:

##EQU15## wherein R_g is a gas constant, T is temperature, η

is viscosity, V is hydrodynamic volume of the probe substance, A is luminescence anisotropy, A_o is a luminescence anisotropy in a "frozen" state, in the absence of Brownian rotation, and τ

is a fluorescence lifetime.

22. Apparatus for measuring concentration of an analyte, comprising:

a) means for directing polarized light to an optical sensor,

b) the optical sensor comprising means for housing a carrier with a high affinity for the analyte, the carrier being conjugated to probe molecules that become luminescent when irradiated, the optical sensor also housing a known quantity of the analyte conjugated to a substance selected from the group consisting of a quencher of luminescence energy of the probe molecules and an energy transfer acceptor of luminescence energy of the probe molecules,

c) the optical sensor being disposed in a medium which contains an unconjugated form of the analyte,

d) means for resolving said luminescence, emitted by the carrier probe molecules, into vector components parallel and perpendicular to a plane of polarization of said polarized light, and for detecting intensities of said vector components, and

e) means for processing the intensities obtained from the resolving and detecting means, the processing means comprising means for calculating a concentration of the unconjugated form of the analyte contacted by the optical sensor, based on values of said intensities.

23. The apparatus of claim 22, wherein the optical sensor contains a viscous medium containing the carrier and the conjugated analyte, the carrier and the conjugated analyte being separated from the unconjugated form of the analyte by a membrane permeable to the analyte in its unconjugated form but impermeable to the conjugated analyte.

24. The apparatus of claim 22, the apparatus further comprising means for determining a topographic distribution of said analyte concentration in said medium.

25. The apparatus of claim 22, wherein the optical sensor comprises a tip and a thermistor, the apparatus further comprising means for correcting anisotropy measurements for temperature of the tip of the sensor by an empirically determined mathematical function.

26. The apparatus of claim 22, the apparatus further comprising means for determining a spatial distribution of said analyte concentration within the medium.

27. Apparatus for measuring concentration of an analyte disposed in a medium, the apparatus comprising:

a) means for directing polarized light towards the medium,

b) the medium including a probe substance which becomes luminescent when irradiated with light, the probe substance being chosen such that its luminescence is quenched by the analyte,

c) means for resolving said luminescence, emitted by the probe substance, into vector components parallel and perpendicular to a plane of polarization of said polarized light, and for detecting intensities of said vector components, and

d) means for processing the intensities obtained from the resolving and detecting means, the processing means comprising means for calculating said concentration of the analyte based on values of said intensities.

28. The apparatus of claim 27, wherein the calculating means comprises means for calculating said analyte concentration according to the following equation:

##EQU16## wherein A is fluorescence anisotropy, defined as ##EQU17## wherein I.sub.

and I.sub.⊥

are intensities of luminescence emission with their electric vectors respectively parallel and perpendicular to the polarized light originating from the directing means, G is an empirical correction factor used to correct for transmission efficiency in parallel and perpendicular planes, R is mean molecular rotation time in radians/sec, A_o is a fluorescence anisotropy in a "frozen" state, in the absence of Brownian an rotation, K_D is a dynamic quench constant, τ

is a luminescence lifetime in the absence of quencher, and is the concentration of the analyte which is to be determined.

29. The apparatus of claim 27, the apparatus further comprising means for determining a topographic distribution of said analyte concentration in the medium.

30. The apparatus of claim 27, further comprising means for correcting anisotropy measurements for temperature according to the following equation:

##EQU18## wherein R_g is a gas constant, T is temperature, η

is viscosity, V is hydrodynamic volume of the probe substance, A is luminescence anisotropy, A_o is luminescence anisotropy in a "frozen" state, in the absence of Brownian rotation, and τ

is fluorescence lifetime.

31. The apparatus of claim 27, the apparatus further comprising means for determining tomographically a topographic distribution of said analyte concentration within the medium by means of optical serial sectioning methodologies.

32. Apparatus for measuring concentration of an analyte disposed in a medium, the apparatus comprising:

a) means for directing polarized light towards the medium,

b) the medium including carriers conjugated with probe molecules which become luminescent when irradiated with light, the medium also including a known quantity of the analyte conjugated with substances selected from the group consisting of a quencher of luminescence energy of the probe molecules and an energy transfer acceptor of luminescence energy of the probe molecules,

c) means for resolving said luminescence, emitted by the probe molecules, into vector components parallel and perpendicular to a plane of polarization of said polarized light, and for detecting intensities of said vector components, and

d) means for processing the intensities obtained from the resolving and detecting means, the processing means comprising means for calculating said concentration of the analyte based on values of said intensities.

33. The apparatus of claim 32, wherein the calculating means comprises means for calculating said analyte concentration according to an empirically determined mathematical function.

34. The apparatus of claim 32, the apparatus further comprising means for determining a topographic distribution of said analyte concentration in the medium.

35. The apparatus of claim 32, further comprising means for correcting anisotropy measurements for temperature of the medium according to an empirically determined function.

36. The apparatus of claim 32, further comprising means for determining tomographically a topographic distribution of said analyte concentration within the medium by means of optical serial sectioning methodologies.