Sensor for Internal Monitoring of Tissue O2 and/or pH/CO2 In Vivo

• US 20110105869A1
• Filed: 11/09/2010
• Published: 05/05/2011
• Est. Priority Date: 01/04/2006
• Status: Abandoned Application

• Current Assignee: Trustees Of The University Of Pennsylvania (University of Pennsylvania)
• Original Assignee: Trustees Of The University Of Pennsylvania (University of Pennsylvania)
• Inventors: Vinogradov, Sergei, Wilson, David F.
• Application Number:
  US12/942,696
• Publication Number:
  US 20110105869A1
• Time in Patent Office: Days
• US Class Current: 600/323
• CPC Class Codes: A61B 5/14539 for measuring pH
• CPC Class Codes: A61B 5/14542 for measuring blood gases A61B5/14551 takes precedence
• CPC Class Codes: A61B 5/1459 invasive, e.g. introduced into the body by a catheter A61B5/1464 takes precedence
• CPC Class Codes: A61B 5/1495 Calibrating or testing of in-vivo probes
• CPC Class Codes: A61B 5/6848 Needles

Abstract

Provided is a durable tissue pH/pCO₂ and/or tissue oxygen sensitive probe of sufficient strength to withstand direct tissue pressures in vivo, the probe comprising one or more sensor chambers within a biocompatible, gas-permeable membrane containing together in a single chamber, or in separate chambers, respectively, a pH sensitive fluorophor from which pCO₂ level(s) are calculated when the fluorophor is excited and the resulting fluorescence is measured and/or an oxygen sensitive phosphor solution producing oxygen quenchable phosphorescence when excited. Further provided is a tissue pH/pCO₂ and/or tissue oxygen detection and measurement system comprising the probe, and methods for use of the probe and the system to directly, rapidly and accurately measure tissue pH/pCO₂ and/or tissue oxygen levels in a patient without reliance on blood vessels or fluid protection of the probe.

Claims

1. An tissue-insertable, in vivo system for real-time measurement of tissue pCO₂ of an animal or human patient, the system comprising:

a fiber optic sensor chamber forming a probe having the wall-strength to withstand external tissue pressure;

a highly fluorescent, aqueous, buffered, pH-sensitive fluorophor, sealed within the fiber optic sensor chamber;

an excitation light source for activating the fluorescence of the fluorophor; and

an instrument for measuring and reporting fluorescence from the activated fluorophor in the fiber optic sensor chamber in place within the tissue of the patient, from which level(s) of pCO₂ are calculated.

2. The system of claim 1, wherein the fluorophor comprises a pH sensitive porphyrin-based dye.

3. The system of claim 1, wherein the pH buffer is bicarbonate buffer, sealed within the fiber optic sensor chamber.

4. The system of claim 1, further comprising optical fibers to 1) transport the excitation light to the fluorophor, and 2) to transport the fluorescence from the fluorophor following excitation to the measuring and reporting instrument.

5. The system of claim 3, further comprising wireless connections to 1) transport the excitation light to the fluorophor, and 2) to transport the fluorescence from the fluorophor following excitation to the measuring and reporting instrument.

6. The system of claim 3, further comprising a combiner for coupling the excitation light source to the optical fiber of the fiber optic sensor chamber.

7. The system of claim 6, further comprising an amplifier to amplify the fluorescence signals.

8. The system of claim 1, further comprising a central processor for calculating and reporting fluorescence measurements.

9. The method of claim 1, further comprising a temperature sensor circuit for measuring temperature at the site of insertion.

20. The system of claim 1, further comprising in the system an element for real-time measurement of tissue oxygen lifetime in the tissue, said system comprising:

a oxygen-quenchable phosphor solution within the probe, wherein refractive index of the phosphor solution is higher than that of the surrounding gas-permeable layer;

an excitation light source for activating the phosphorescence of the phosphor; and

an instrument for measuring and reporting phosphorescence from the activated phosphor from within the tissue of the patient.

21. The system of claim 20, wherein the phosphor comprises an aqueously soluble oxygen quenching, dendrimeric metalloporphyrin sensor, which is capable of phosphorescence, and having the formula:

10. A tissue-insertable probe device containing therein a fluororphor analyte within a sealed sensor chamber, wherein the fluorophor operably responds to pH levels in the surrounding tissue, thereby providing calculated pCO₂ levels in the tissue.

11. The probe of claim 10, further comprising one or more aligned optic fibers, each having two opposing ends, and each of which is operably connected and sealed at the distal end to the probe, thereby forming an operably-linked light guide for collecting emitted fluorescence from the fluorophor at less than the numerical aperture of the light guide;

wherein at the proximal end, at least one first fiber is externally, operably-connected to the light source to transmit excitation light to the fluorophor within the sealed sensor chamber, and wherein at least one second fiber is externally connected to the detecting device to collect and transmit emitted fluorescence from the fluorophor to the detector device.

22. The probe of claim 10 further comprising:

a phosphor solution within the probe, wherein refractive index of the phosphor solution is higher than that of the surrounding gas-permeable layer;

an excitation light source for activating the phosphorescence of the phosphor; and

an instrument for measuring and reporting phosphorescence from the activated phosphor from within the tissue of the patient.

23. The probe of claim 22, wherein the phosphor comprises an aqueously soluble oxygen quenching, dendrimeric metalloporphyrin sensor, which is capable of phosphorescence, and having the formula:

12. A method for making real-time, in vivo measurement of tissue pCO₂ in the animal or human patient, the method comprising:

inserting into the tissue of a patient the probe containing the sealed fiber optic sensor chamber containing the buffered, pH sensitive fluorophor into the tissue;

activating the excitation light source to excite the fluorophor;

measuring the fluorescence from the excited fluorophor; and

calculating pCO₂ from the pH measurement.

13. The method of claim 12, wherein the fluorophor comprises a pH sensitive porphyrin-based dye.

14. The method of claim 12, wherein the pH buffer is bicarbonate buffer.

15. The method of claim 12, further comprising connecting optical fibers to 1) transport the excitation light to the fluorophor within the sensor chamber, and 2) to transport the fluorescence from the fluorophor following excitation to the measuring and reporting instrument.

16. The method of claim 15, further comprising connecting a combiner for coupling the excitation light source to the optical fiber of the fiber optic sensor chamber.

17. The method of claim 16, further comprising connecting an amplifier to amplify the fluorescence signals.

18. The method of claim 12, further comprising connecting a central processor for calculating and reporting fluorescence measurements.

19. The method of claim 12, further comprising connecting a temperature sensor circuit for measuring temperature at the site of insertion, and measuring temperature.

24. A method of using the system of claim 12 for also making real-time, in vivo measurement of tissue pO₂ and oxygen pressure in the animal or human patient, the method comprising:

adding an oxygen quenchable phosphor solution into the probe containing the sealed fiber optic sensor chamber containing the buffered, pH sensitive fluorophor, or adding a second sealed fiber optic sensor chamber containing the oxygen quenchable phosphor solution into the probe;

inserting the probe into the tissue;

activating the excitation light source to activate the phosphor as well as the fluorophor and the phosphor;

measuring and reporting the phosphorescence from the excited phosphor for real-time measurement of tissue oxygen lifetime in the tissue as well as the fluorescence from the excited fluorophor.

25. The method of claim 24, wherein the phosphor comprises an aqueously soluble oxygen quenching, dendrimeric metalloporphyrin sensor, which is capable of phosphorescence, and having the formula:

26. The method of claim 25, further comprising one or more of the additional steps consisting of connecting optical fibers to 1) transport the excitation light to the phosphor within the sensor chamber, and 2) to transport the phosphorescence from the phosphor following excitation to the measuring and reporting instrument;

connecting a combiner for coupling the excitation light source to the optical fiber of the fiber optic sensor chamber;

connecting an amplifier to amplify the phosphorescence signals; and

connecting a central processor for calculating and reporting phosphorescence measurements.

27. The method of claim 12, further comprising monitoring oxygen supplied to the patient'"'"'s ischemic bowel, to the patient'"'"'s surgically transplanted muscle flap or to the patient'"'"'s tissue during cardiopulmonary resuscitation.