Low-potential electrochemical redox sensors

• US 4,805,624 A
• Filed: 04/14/1987
• Issued: 02/21/1989
• Est. Priority Date: 09/09/1985
• Status: Expired due to Term

• Current Assignee: University Of Pittsburgh Medical Center (Western Maryland Health System Corp.)
• Original Assignee: Montefiore Hospital Association Of Western Pennsylvania
• Inventors: Wolfson, Sidney K. Jr., Yao, Shang J.
• Primary Examiner(s): Coven, Edward M.
• Application Number:
  US07/037,976
• Time in Patent Office: 679 Days
• Field of Search: 128/635-640, 204/1 K, 204/5 T, 204/403, 204/406, 204/422, 204/415
• US Class Current: 600/345
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: G01N 27/3277 being a redox reaction, e.g. detection by cyclic voltammetry voltammetry per se G01N27/42, G01N27/48

Abstract

Improved low-potential electrochemical sensors and method for rapid, accurate, in vitro and in vivo measurement of the concentration of carbohydrates in organic or biological fluids by cyclic voltammetric or coulometric scan within a restricted voltage domain and identifying one or more oxidation and/or reduction current peaks, with the concentration of the carbohydrate being a linear function of the current output. Two well defined, sharp, distinctly separated, specific, reproducable and interference-free peaks have been discovered in the low-potential voltage domain of -0.9V to -0.2V, cathodic reduction Peak 1 and anodic oxidation Peak 2 in the range of -0.70V to -0.90V. The scan is pulsed or a steady sweep, and sensitivity increases with increased scan rate in the range of 30-50 mV/sec. Pulses may range on the order of 20-50 millisecond in duration, and sampling during the last 1.5 milliseconds of the pulse restricts values to pure oxidation/reduction currents. Cyclic and/or pulsed scanning regenerates the electrodes making the sensor drift free. A system is disclosed employing the sensor as part of an implantable insulin pump which is microprocessor controlled, thus functioning as an artificial pancreas. The sensors can also be used in bedside monitoring systems as an indwelling sensor introduced by catheterization, for in-line extracorporeal shunt systems, or for non-invasive measurement of carbohydrate levels.

Claims

1. An improved electrochemical redox sensor for precise in vitro and in vivo measurement of one or more carbohydrates present in organic and biological fluids and tissues by cyclic voltammetric or coulometric scanning, comprising in operative combination:

(a) a cell having;

(i) a first, working electrode adapted to permit contact with a test specimen of said carbohydrate being measured, said test specimen exhibiting at least one voltage peak upon said cyclic scanning;

(ii) a second, counter electrode;

(iii) a third, reference electrode;

(iv) said working electrode being disposed to contact one or more carbohydrates present in a test specimen, and said second and said third electrodes being in ionic contact with each other and with said first electrode;

(b) means for providing a current to said working electrode and withdrawing it from said counter electrode;

(c) means for cyclic scan of said cell within a low potential far negative voltage domain of -0.9 V to -0.2 V vs. silver/silver chloride;

(d) means for sensing the amount of current flow between said working and said counter electrodes for at least one voltage peak exhibited by said test specimen when scanned in said voltage domain, said voltage peak being selected from a cathodic reduction peak and an anodic oxidation peak, said peak being present in the range of about -0.70 V to -0.90 V vs. silver/silver chloride at 37 C; and

(e) means for correlating said test specimen peak height sensed to a value of carbohydrate in said test specimen.

2. A sensor as in claim 1 wherein:

(a) said scan rate controlling means includes means providing a pulsed scan at least at said voltage peak.

3. A sensor as in claim 2 which includes:

(a) means for selectively controlling said scan rate in the range of from about 30 mV/sec to about 50 mV/sec.

4. A sensor as in claim 3 wherein:

(a) said cyclic scan means includes means providing a steady sweep scan.

5. A sensor as in claim 2 which:

(a) includes means for sampling current during the last about 1.5 milliseconds of said pulse at said peak.

6. A sensor as in claim 5 wherein said pulse duration is on the order of 20-50 milliseconds.

7. A sensor as in claim 6 wherein:

(a) said working electrode is selected from wire, disc and metal film deposited on a biologically acceptable support.

8. A sensor as in claim 6 wherein:

(a) said cell includes means for in vivo implantation comprising a tissue compatible material covering at least a portion of said first, working electrode.

9. A sensor as in claim 6 wherein:

(a) said cell includes means for removably introducing at least said first, working electrode into a patient'"'"'s body for positioning therein as an indwelling sensor for bedside monitoring.

10. A sensor as in claim 5 wherein:

(a) said cell includes means for in vivo implantation comprising a tissue compatible material covering at least a portion of said first, working electrode.

11. A sensor as in claim 5 wherein:

(a) said cell includes means for removably introducing at least said first, working electrode into a patient'"'"'s body for positioning therein as an indwelling sensor for bedside monitoring.

12. A sensor as in claim 2 wherein:

(a) said working electrode is selected from smooth platinum, platinum-black, palladium, palladium-black, rhodium, rhodium-black and alloys of platinum, iridium, and palladium.

13. A sensor as in claim 12 wherein:

(a) said cell includes means for in vivo implantation comprising a tissue compatible material covering at least a portion of said first, working electrode.

14. A sensor as in claim 12 wherein:

(a) said cell includes means for removably introducing at least said first, working electrode into a patient'"'"'s body for positioning therein as an indwelling sensor for bedside monitoring.

15. A sensor as in claim 2 wherein:

(a) said cell includes means for in vivo implantation comprising a tissue compatible material covering at least a portion of said first, working electrode.

16. A sensor as in claim 2 wherein:

(a) said cell includes means for removably introducing at least said first, working electrode into a patient'"'"'s body for positioning therein as an indwelling sensor for bedside monitoring.

17. A sensor as in claim 1 wherein:

(a) said cell includes means for in vivo implantation comprising a tissue compatible material covering at least a portion of said first, working electrode.

18. A sensor as in claim 1 wherein:

(a) said cell includes means for removably introducing at least said first, working electrode into a patient'"'"'s body for positioning therein as an indwelling sensor for bedside monitoring.