Biomedical fiber optic probe with frequency domain signal processing

• US 5,127,405 A
• Filed: 02/16/1990
• Issued: 07/07/1992
• Est. Priority Date: 02/16/1990
• Status: Expired due to Fees

• Current Assignee: Ohmeda Pte Limited
• Original Assignee: BOC Group Pty Limited (Linde Plc)
• Inventors: Atwater, Beauford W., Alcala, J. Ricardo
• Primary Examiner(s): Kamm, William E.
• Assistant Examiner(s): Pontius, Kevin
• Application Number:
  US07/481,131
• Time in Patent Office: 872 Days
• Field of Search: 128/633, 128/634, 128/665, 128/666, 128/667
• US Class Current: 600/342
• CPC Class Codes: A61B 5/14555 specially adapted for the eye fundus
• CPC Class Codes: A61B 5/1459 invasive, e.g. introduced into the body by a catheter A61B5/1464 takes precedence
• CPC Class Codes: A61B 5/6855 with a distal curved tip
• CPC Class Codes: G01N 21/6408 with measurement of decay time, time resolved fluorescence

Abstract

A fiber optic probe incorporating a luminescent composition is used to monitor conditions within a living subject. Response light from the fiber optic is detected and a frequency domain representation of the response light is derived. Characteristics of the frequency domain representation are used to derive values for luminescence lifetimes or similar decay parameters and these values in turn are translated into values of the conditions to be sensed.

Claims

1. Apparatus for monitoring conditions within a living subject comprising:

(a) a probe adapted for insertion into the body of a subject, said probe including an elongated optically transmissive fiber having a proximal end and a distal end, said probe also including a luminescent composition mounted at said distal end of said fiber in optical communication therewith, said luminescent composition having one or more luminescent decay time parameters affected by said condition when said distal end of said probe is disposed within the body of a subject;

(b) means for applying to said composition through said fiber excitation light varying cyclically in amplitude, said excitation light incorporating components varying in amplitude at a plurality of excitation modulation frequencies simultaneously, whereby said luminescent composition will emit response light varying cyclically in amplitude and including a plurality of response components varying in amplitude at a plurality of response modulation frequencies simultaneously and said response light will be transmitted through said fiber to said proximal end thereof;

(c) means for detecting the cyclically varying amplitude of said response light transmitted to said proximal end of said fiber and deriving a frequency domain representation of said cyclically varying response light amplitude including at least one characteristic of each of said plurality of response components; and

(d) means for deriving values of one or more luminescence decay parameters of said composition from said characteristics, whereby said derived luminescence delay parameters will vary with said conditions.

2. Apparatus as claimed in claim 1 wherein said luminescence composition has one or more rapidly decaying luminescence modes having decay time less than about 100 nanoseconds and wherein said means for detecting said cyclically varying response light amplitude and deriving a frequency domain representation include means for deriving a frequency domain representation of components in said response light representing said one or more rapidly decaying luminescence modes.

3. Apparatus as claimed in claim 1 wherein said means for detecting said cyclically varying response light amplitude and deriving a frequency domain representation include means for directly sampling the amplitude of said response light and providing a response series of digital sample values each representing the amplitude of said response light at a predetermined point in the repetitive response light cycle, and a means for transforming said response series of digital sample values into said frequency domain representation.

4. Apparatus as claimed in claim 3 wherein said means for transforming includes means for applying a digital Fourier transform to said response series of sample values.

5. Apparatus as claimed in claim 3 wherein said means for sampling the amplitude of said light includes means for sampling said response light over a plurality of cycles of said response light to provide raw sample values from said plural cycles and means for averaging raw sample values from a plurality of cycles to provide each value in said response series of sample values.

6. Apparatus as claimed in claim 3 wherein said means for providing said response series of sample values includes means for providing a plurality of said response series of sample values and said means for transforming includes means for applying a transformation independently to each said response series of sample values to thereby provide a plurality of frequency domain representations of said response light each including said at least one characteristic of each of said plurality of response components, said means for deriving a frequency domain representation further comprising means for averaging values of each said characteristic in a plurality of said independent frequency domain representations to derive an averaged frequency domain representation, said means for deriving luminescent decay parameters from said characteristics including means for deriving said luminescent decay parameters from said characteristics in said averaged frequency domain representation.

7. Apparatus as claimed in claim 3 wherein said means for sampling said response light includes means for sampling said response light at a frequency lower than the lowest one of said excitation modulation frequencies.

8. Apparatus as claimed in claim 1 wherein said means for deriving a frequency domain representation includes means for deriving a phase angle for each said response component, and said means for deriving one or more luminescence decay parameters includes means for deriving said parameters at least in part from said phase angles.

9. Apparatus as claimed in claim 8 wherein said means for deriving one or more luminescence decay parameters includes means for deriving one or more decay exponents from said phase angles.

10. Apparatus as claimed in claim 1 wherein said means for deriving a frequency domain representation includes means for deriving a modulation value for each said response component, and said means for deriving one or more luminescence decay parameters includes means for deriving said parameters at least in part from said modulation values.

11. Apparatus as claimed in claim 1 wherein said fiber has a diameter less than about 450 micrometers.

12. Apparatus as claimed in claim 11 wherein said probe includes a plurality of fibers and said probe has an overall diameter less than about 450 micrometers.

13. Apparatus as claimed in claim 11 wherein said luminescent composition is disposed in a mass abutting the distal end of said fiber and wherein said mass has a maximum dimension in the direction transverse to the direction of elongation of said fiber less than about 450 micrometers.

14. Apparatus as claimed in claim 1 wherein said luminescent composition includes a luminescent material dispersed in a polymer.

15. Apparatus as claimed in claim 14 wherein said luminescent material is sensitive to oxygen and wherein said polymer is selected from the group consisting polyurethanes, polysiloxanes, polysiloxanepolycarbonate copolymers and combinations thereof.

16. Apparatus as claimed in claim 14 wherein said luminescent material is a compound selected from the group consisting of porphyrin;

chlorin, bacteriochlorin, phosphorinogen and derivatives and combinations thereof.

17. A method of monitoring conditions within a living subject comprising the steps of:

(a) inserting a probe including an elongated optically transmissive fiber and a luminescent composition mounted at a distal end of the fiber in optical communication therewith, into the body of the subject so that the distal end of the fiber is disposed within the body and one or more luminescent decay time parameters of the composition are affected by the condition to be monitored, and so that a proximal end of the fiber is disposed outside of the body;

(b) directing excitation light through said fiber to said composition, said excitation light varying cyclically in amplitude, and incorporating components varying in amplitude at a plurality of excitation modulation frequencies simultaneously, whereby said luminescent composition will emit response light varying cyclically and including a plurality of response components varying in amplitude at a plurality of response modulation frequencies simultaneously and said response light will be transmitted through said fiber to said proximal end thereof;

(c) detecting the cyclically varying amplitude of said response light transmitted to said proximal end of said fiber;

(d) deriving a frequency domain representation of said cyclically varying response light amplitude including at least one characteristic of each of said plurality of response components; and

(e) deriving a value of one or more luminescence decay parameters of said composition from said characteristics, whereby said derived luminescence delay parameters will vary with said conditions.

18. A method as claimed in claim 17 further comprising the step of translating said one or more derived luminescence decay parameters into a value of the condition to be monitored.

19. A method as claimed in claim 17 wherein one or more luminescence decay parameters include a decay time less than about 100 monoseconds.

20. A method as claimed in claim 17 wherein said step of detecting the cyclically varying amplitude of said response light and deriving a frequency domain representation includes the step of sampling the amplitude of said response light and providing a response series of sample values in digital form so that each said response light at a predetermined point in the repetitive response light cycle, and transforming said response series of sample values into said frequency domain representation.

21. A method as claimed in claim 20 wherein said step of transforming includes the step of applying a digital Fourier transform to said response series of sample values.

22. A method as claimed in claim 20 wherein said step of sampling the amplitude of said response light includes steps of sampling the response light over a plurality of cycles of said response light to provide raw sample values from said plural cycles and averaging raw sample values from a plurality of cycles to provide each value in said response series of sample values.

23. A method as claimed in claim 20 wherein said step of providing said response series of sample values includes the step of sampling the amplitude of said response light repeatedly to provide a plurality of said response series of sample values and said transforming step includes the step of applying a transformation independently to each said response series of sample values to thereby provide a plurality of frequency domain representations of said response light, each such representation including said at least one characteristic of each of said plurality of response components, said step of deriving a frequency domain representation further including the step of averaging values of each said characteristic in a plurality of said independent frequency domain representations to derive an average frequency domain representation, said step of deriving luminescent decay parameters from said characteristics including the step of deriving said luminescent decay parameters from said characteristics in said averaged frequency domain representation.

24. A method as claimed in claim 20 wherein said step of applying excitation light includes the step of applying said excitation light as a series of pulses at a fundamental frequency whereby said response light will include components varying in amplitude at said fundamental frequency and at harmonics thereof, and wherein said step of sampling the amplitude of said response light includes the step of sampling the amplitude of said response light at a sampling frequency lower than said fundamental frequency.

25. A method as claimed in claim 20 wherein said step of deriving a frequency domain representation includes the step of deriving a phase angle for each said response component, and said step of deriving one or more luminescence decay parameters includes the step of deriving said parameters at least in part from said phase angles.

26. A method as claimed in claim 20 wherein said step of the deriving a frequency domain representation includes the step of deriving a modulation value for each said response component, and wherein said step of deriving one or more luminescence decay parameters includes the step of deriving said parameters at least in part from said modulation values.

27. A method as claimed in claim 17 wherein said condition is the PO₂ of the blood in a mammal.

28. A method as claimed in claim 17 wherein said condition is the pH of the blood in a mammal.

29. A method as claimed in claim 17 wherein said condition is the PCO₂ of the blood in a mammal.

30. A method as claimed in claim 17 wherein said probe includes a plurality of optically transmissive fibers each having a luminescent composition mounted at the digital end thereof, each said luminescent composition being sensitive to a different condition to be sensed, said step of inserting said probe including the step of positioning all of said luminescent compositions within said subject, said step of directing excitation light, and response light including the steps of directing excitation light along each of said fibers, said step of detecting the cyclically varying amplitude of said response light including the step of detecting the amplitude of response light transmitted to the proximal end of each fiber, said step of deriving a frequency domain representation including the step of deriving a frequency domain representation of the response light amplitude from at least one of said fibers.