Emission quenching sensors

• US 5,518,694 A
• Filed: 05/30/1995
• Issued: 05/21/1996
• Est. Priority Date: 10/14/1993
• Status: Expired due to Fees

• Current Assignee: Terumo Cardiovascular Systems Corporation (Terumo Corporation)
• Original Assignee: 3M Company
• Inventors: Bentsen, James G.
• Primary Examiner(s): Snay, Jeffrey R.
• Application Number:
  US08/454,055
• Time in Patent Office: 357 Days
• Field of Search: 422/82.07, 422/82.08, 422/79, 422/91, 436/172, 250/458.1
• US Class Current: 422/82.08
• CPC Class Codes: G01N 2021/6432 Quenching
• CPC Class Codes: G01N 21/274 Calibration, base line adjustment, drift correction
• CPC Class Codes: G01N 21/6408 with measurement of decay time, time resolved fluorescence
• CPC Class Codes: G01N 21/643 non-biological material
• CPC Class Codes: Y10T 436/207497 Molecular oxygen
• CPC Class Codes: Y10T 436/209163 Dissolved or trace oxygen or oxygen content of a sealed environment

Abstract

The present invention relates to a sensing instrument and method for measuring the concentration of an analyte. The sensing instrument includes: a sensing element including at least a first emissive indicator characterized by a bimolecular quenching rate constant k_q, one or more fluorescence lifetimes τ_o above a lowest lifetime τ_oL, and capable of emitting analyte concentration dependent signals when exposed to an excitation signal in the presence of quencher; an excitation system which provides an amplitude modulated excitation signal at one or more radial modulation frequencies ω; a detector; and a processor. The processor univariantly processes the detected signals and provides output signals representative of analyte concentration. The sensing element and/or excitation system are configured to enable the instrument to operate sufficiently within the condition [(k_q [Q])² +ω² ]τ_o² >>1+2k_q τ_o [Q] such that a slope of the relationship between the concentration dependent parameter and analyte concentration is independent of τ_o variability and/or heterogeneity for all analyte concentrations within the operating range and for all lifetimes τ _o greater than τ_oL.

Claims

1. An instrument for measuring the concentration of an analyte within an operating range of interest, comprising:

a sensing element comprising a matrix material and an emissive indicator, wherein said matrix material is permeable to a quencher comprising said analyte or a substance related to said analyte by a known relationship, and wherein said emissive indicator has a bimolecular quenching rate constant k_q for said quencher, one or more fluoresence liftimes τ

_o above a lowest lifetime τ

_oL, and capable of emitting analyte concentration dependent signals having a concentration dependent parameter which varies as a function of analyte concentration when exposed to a excitation signal in the presence of quencher;

an excitation system coupled to the sensing element for providing the excitation signal at one or more radial frequencies ω

;

a detector coupled to the sensing element for detecting the analyte concentration dependent signal(s) and for providing detected signal(s);

a processor including memory for storing calibration information characterizing a relationship between analyte concentration and the first concentration dependent parameter, for univariantly processing the first detected signal(s) to derive the first concentration dependent parameter and providing output signal(s) representative of analyte concentration as a function of the derived concentration dependent parameter and the stored calibration information; and

wherein the sensing element and excitation system are configured to enable the instrument to operate sufficiently within the operating condition where the quantity {[(k_q [Q])² +ω

² ]τ

_o² } is greater than 4 times the quantity {1+2k_q τ

_o [Q]} for all analyte concentrations within the operating range of interest and for all lifetimes τ

_o greater than τ

_oL, where [Q] is the concentration of said quencher in said matrix.

2. The instrument of claim 1, wherein the frequency of said excitation signal provides an operating condition where the quantity ω

τ

_o is greater than 4 for all analyte concentrations within the operating range of interest and for all lifetimes τ

_o greater than τ

_oL, and wherein said analyte and said quencher are oxygen.

3. The instrument of claim 1, wherein the frequency of said excitation signal provides an operating condition where the quantity ω

τ

_o is greater than 6 for all analyte concentrations within the operating range of interest and for all lifetimes τ

_o greater than τ

_oL, and wherein said matrix comprises a polymer.

4. The instrument of claim 1, wherein the sensing element is configured to provide an operating condition where the quantity k_q τ

_o [Q] is greater than 10 for all analyte concentrations within the operating range of interest and for all lifetimes τ

_o greater than τ

_oL.

5. The instrument of claim 1, wherein the sensing element is configured to provide an operating condition where the quantity k_q τ

_o [Q] is greater than 15 for all analyte concentrations within the operating range of interest and for all lifetimes τ

_o greater than τ

_oL, and wherein said analyte is selected from the group consisting of oxygen, ionized hydrogen, and carbon dioxide.

6. The instrument of claim 1, wherein the sensing element is configured to provide an operating condition where the quantity k_q τ

_o [Q] is greater than 20 for all analyte concentrations within the operating range of interest and for all lifetimes τ

_o greater than τ

_oL, and wherein said analyte and said quencher are oxygen.

7. The instrument of claim 1, wherein said concentration dependent parameter is the modulated frequency required to provide a constant phase shift or demodulation factor.

8. The instrument of claim 1, wherein the frequency of said excitation signal provides an operating condition where the quantity ω

τ

_o is greater than 10 for all analyte concentrations within the operating range of interest and for all lifetimes τ

_o greater than τ

_oL.

9. The instrument of claim 8, wherein said excitation system comprises a light source selected from the group consisting of light emitting diodes, laser diodes, frequency doubled laser diodes, and solid state light sources.

10. The instrument of claim 8, wherein said sensing element is configured to operate within the a-line circuit of an arterial catheter.

11. The instrument of claim 1, wherein the sensing element and excitation signal are configured so as to provide an operating condition where the quantity {[(k_q [Q])² +ω

² ]τ

_o² } is greater than 6 times the quantity {1+2k_q τ

_o [Q]} for all analyte concentrations within the operating range of interest and for all lifetimes τ

_o greater than τ

_oL, and wherein said matrix comprises a polymer.

12. The instrument of claim 11, wherein said excitation signal has a constant radial frequency ω

₁ and said sensing element emits analyte concentration dependent signals which are phase shifted by Δ

θ

₁ and demodulated by a demodulation factor m₁ with respect to said excitation signal, and wherein said processor univariantly processes said detected signals to derive the phase shift between said emitted signal and said excitation signal.

13. The instrument of claim 12, wherein said processor includes stored information characterizing a relationship between analyte concentration and the phase shift between one of said analyte concentration dependent signals and said excitation signal, univariantly processes the detected signal(s) to derive said phase shift, and provides output signal(s) representative of analyte concentration as a function of said stored information and said derived phase shift.

14. The instrument of claim 1, wherein the sensing element and excitation signal are configured so as to provide an operating condition where the quantity {[(k_q [Q])² +ω

² ]τ

_o² } is greater than 10 times the quantity {1+2k_q τ

_o [Q]} for all analyte concentrations within the operating range of interest and for all lifetimes τ

_o greater than τ

_oL.

15. The instrument of claim 14, wherein said emissive indicator comprises at least two monomeric components wherein at least one of said monomeric components is a monomeric indicator component and wherein said sensing element, when exposed to said excitation signal, provides a first emission signal from an unreacted first excited state and a second emission signal from a reacted second excited state complex produced in said sensing element from said monomeric components, and wherein said processor univariantly processes said first emitted signal or said second emitted signal or said first and second emitted signals to determine the concentration of said analyte.

16. The instrument of claim 15, wherein said processor includes stored information characterizing a relationship between analyte concentration and the phase shift difference between the first analyte concentration dependent signal and the second analyte concentration dependent signal, univariantly processes the detected signal(s) to derive said phase shift difference, and provides output signal(s) representative of analyte concentration as a function of said stored information and said derived phase shift difference.

17. An instrument for measuring the concentration of an analyte within an operating range of interest, comprising:

a sensing element comprising an emissive indicator configured for exposure to a quencher, said quencher comprising said analyte or a substance related to said analyte by a known relationship, and wherein said emissive indicator is characterized by a bimolecular quenching rate constant k_q for said quencher, one or more fluoresence liftimes τ

_o above a lowest lifetime τ

_oL, and capable of emitting analyte concentration dependent signals having a concentration dependent parameter which varies as a function of analyte concentration when exposed to a excitation signal in the presence of quencher;

an excitation system coupled to the sensing element for providing the excitation signal at one or more radial frequencies ω

;

a detector coupled to the sensing element for detecting the analyte concentration dependent signal(s) and for providing detected signal(s);

a processor including memory for storing calibration information characterizing a relationship between analyte concentration and the concentration dependent parameter, for univariantly processing the detected signal(s) to derive the concentration dependent parameter and providing output signal(s) representative of analyte concentration as a function of the derived concentration dependent parameter and the stored calibration information; and

wherein the sensing element and excitation system are configured to enable the instrument to operate sufficiently within the operating condition where the quantity {[(k_q [Q])² +ω

² ]τ

_o² } is sufficiently greater than the quantity {1+2k_q τ

_o [Q]} such that a slope of the relationship between the concentration dependent parameter and analyte concentration is independent of τ

_o variability for all analyte concentrations within the operating range of interest and for all lifetimes τ

_o greater than τ

_oL, where [Q] is the concentration of said quencher in said sensing element.

18. The instrument of claim 17, wherein said analyte is selected from the group consisting of oxygen, ionized hydrogen, and carbon dioxide.

19. An instrument for measuring the concentration of oxygen within an operating range of interest, comprising:

a sensing element comprising a matrix material having an oxygen solubility constant a, and an emissive indicator, wherein said matrix material is permeable to oxygen, and wherein said emissive indicator has a bimolecular quenching rate constant k_q for oxygen, one or more fluoresence liftimes τ

_o above a lowest lifetime τ

_oL, and capable of emitting oxygen concentration dependent signals having a concentration dependent parameter which varies as a function of oxygen concentration when exposed to a excitation signal in the presence of quencher;

an excitation system coupled to the sensing element for providing the excitation signal at one or more radial frequencies ω

;

a detector coupled to the sensing element for detecting the oxygen concentration dependent signal(s) and for providing detected signal(s);

a processor including memory for storing calibration information characterizing a relationship between oxygen concentration and the first concentration dependent parameter, for univariantly processing the first detected signal(s) to derive the first concentration dependent parameter and providing output signal(s) representative of oxygen concentration as a function of the derived concentration dependent parameter and the stored calibration information; and

wherein the sensing element and excitation system are configured to enable the instrument to operate sufficiently within the operating condition where the quantity {[(ak_q P_o2)² +ω

² ]τ

o² } is greater than 4 times the quantity {1+2ak_q τ

_o P_o2 } for all oxygen concentrations within the operating range of 40 to 200 mm Hg and for all lifetimes τ

o greater than τ

oL.

20. The instrument of claim 19, wherein said sensing element and said excitation signal are configured so as to provide an operating condition where the quantity {[(ak_q P_o2)² +ω

² ]τ

_o² } is greater than 6 times the quantity (1+2ak_q τ

_o P_o2 } for all oxygen partial pressures within the operating range of 40 to 120 mm Hg and for all lifetimes τ

_o greater than τ

_oL.

21. The instrument of claim 19, wherein said oxygen permeable matrix comprises a silicone polymer and said emissive indicator comprises a polyaromatic hydrocarbon.

22. The instrument of claim 19, wherein said emissive indicator comprises at least two monomeric components wherein at least one of said monomeric components is a monomeric indicator component and wherein said sensing element, when exposed to said excitation signal, provides a first emission signal from an unreacted first excited state and a second emission signal from a reacted second excited state complex produced in said sensing element from said monomeric components, and wherein said first emitted signal or said second emitted signal or said first and second emitted signals are univariantly processed to determine the concentration of said analyte.

23. The instrument of claim 19, wherein the frequency of said excitation signal provides an operating condition where the quantity ω

τ

_o is greater than 10 for all oxygen concentrations within the operating range of 40 to 200 mm Hg and for all lifetimes τ

_o greater than τ

_oL.

24. The instrument of claim 19, wherein the sensing element is configured to provide an operating condition where the quantity ak_q τ

_o P_o2 is greater than 10 for all oxygen concentrations within the operating range of 40 to 200 mm Hg and for all lifetimes τ

_o greater than τ

_oL.

25. The instrument of claim 19, wherein said excitation signal has a constant radial frequency ω

₁ and said sensing element emits analyte concentration dependent signals which are phase shifted by Δ

θ

₁ and demodulated by a demodulation factor m₁ with respect to said excitation signal, and wherein said processor univariantly processes said detected signals to derive the phase shift between said emitted signal and said excitation signal.

26. The instrument of claim 19, wherein said medium is blood.

27. The instrument of claim 19, wherein said sensing element and said excitation signal are configured so as to provide an operating condition where the quantity {[(ak_q P_o2)² +ω

² ]τ

_o² } is greater than 10 times the quantity {1+2ak_q τ

_o P_o2 } such that a slope of the relationship between the concentration dependent parameter and oxygen partial pressure is independent of τ

_o variability or heterogeneity or both for all oxygen partial pressures within the operating range of 40 to 200 mm Hg and for all lifetimes τ

_o greater than τ

_oL.

28. The instrument of claim 27, wherein the sensing element is configured to provide an operating condition where the quantity ak_q τ

_o P_o2 is greater than 10 such that the intercept of the relationship between the concentration dependent parameter and oxygen partial pressure is independent of τ

_o variability or heterogeneity or both.